33 results on '"Martins TR"'
Search Results
2. 180 Erector spinae plane block for tram – on the way to eras?
- Author
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Montenegro Ledo, LA, primary, Santos Almeida Silva, AR, additional, Alves Martins, TR, additional, Rodrigues, I, additional, Cunha Gomes Santos, HM, additional, and Pereira, EC, additional
- Published
- 2021
- Full Text
- View/download PDF
3. 114 Pheochromocytoma and C-section – is regional anaesthesia the solution for this dangerous combination?
- Author
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Montenegro Ledo, LA, primary, Alves Martins, TR, additional, Santos Almeida Silva, AR, additional, Sanches Lucas, MP, additional, and Pereira, EC, additional
- Published
- 2021
- Full Text
- View/download PDF
4. Long-range two-particle correlations of strange hadrons with charged particles in pPb and PbPb collisions at LHC energies
- Author
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Khachatryan, V[ 1 ], Sirunyan, AM[ 1 ], Tumasyan, A[ 1 ], Adam, W[ 2 ], Bergauer, T[ 2 ], Dragicevic, M[ 2 ], Ero, J[ 2 ], Fabjan, C[ 2 ], Friedl, M[ 2 ], Fruhwirth, R[ 2 ], Ghete, VM[ 2 ], Hartl, C[ 2 ], Hormann, N[ 2 ], Hrubec, J[ 2 ], Jeitler, M[ 2 ], Kiesenhofer, W[ 2 ], Knunz, V[ 2 ], Krammer, M[ 2 ], Kratschmer, I[ 2 ], Liko, D[ 2 ], Mikulec, I[ 2 ], Rabady, D[ 2 ], Rahbaran, B[ 2 ], Rohringer, H[ 2 ], Schofbeck, R[ 2 ], Strauss, J[ 2 ], Taurok, A[ 2 ], Treberer Treberspurg, W[ 2 ], Waltenberger, W[ 2 ], Wulz, CE[ 2 ], Mossolov, V[ 3 ], Shumeiko, N[ 3 ], Gonzalez, JS[ 3 ], Alderweireldt, S[ 4 ], Bansal, M[ 4 ], Bansal, S[ 4 ], Cornelis, T[ 4 ], De Wolf, EA[ 4 ], Janssen, X[ 4 ], Knutsson, A[ 4 ], Luyckx, S[ 4 ], Ochesanu, S[ 4 ], Rougny, R[ 4 ], De Klundert, MV[ 4 ], Van Haevermaet, H[ 4 ], Van Mechelen, P[ 4 ], Van Remortel, N[ 4 ], Van Spilbeeck, A[ 4 ], Blekman, F[ 5 ], Blyweert, S[ 5 ], D'Hondt, J[ 5 ], Daci, N[ 5 ], Heracleous, N[ 5 ], Keaveney, J[ 5 ], Lowette, S[ 5 ], Maes, M[ 5 ], Olbrechts, A[ 5 ], Python, Q[ 5 ], Strom, D[ 5 ], Tavernier, S[ 5 ], Van Doninck, W[ 5 ], Van Mulders, P[ 5 ], Van Onsem, GP[ 5 ], Villella, I[ 5 ], Caillol, C[ 6 ], Clerbaux, B[ 6 ], De Lentdecker, G[ 6 ], Dobur, D[ 6 ], Favart, L[ 6 ], Gay, APR[ 6 ], Grebenyuk, A[ 6 ], Leonard, A[ 6 ], Mohammadi, A[ 6 ], Pernie, L[ 6 ], Reis, T[ 6 ], Seva, T[ 6 ], Thomas, L[ 6 ], Velde, CV[ 6 ], Vanlaer, P[ 6 ], Wang, J[ 6 ], Zenoni, F[ 6 ], Adler, V[ 7 ], Beernaert, K[ 7 ], Benucci, L[ 7 ], Cimmino, A[ 7 ], Costantini, S[ 7 ], Crucy, S[ 7 ], Dildick, S[ 7 ], Fagot, A[ 7 ], Garcia, G[ 7 ], Mccartin, J[ 7 ], Rios, AAO[ 7 ], Ryckbosch, D[ 7 ], Diblen, SS[ 7 ], Sigamani, M[ 7 ], Strobbe, N[ 7 ], Thyssen, F[ 7 ], Tytgat, M[ 7 ], Yazgan, E[ 7 ], Zaganidis, N[ 7 ], Basegmez, S[ 8 ], Beluffi, C[, 8, 190, ], Bruno, G[ 8 ], Castello, R[ 8 ], Caudron, A[ 8 ], Ceard, L[ 8 ], Da Silveira, GG[ 8 ], Delaere, C[ 8 ], du Pree, T[ 8 ], Favart, D[ 8 ], Forthomme, L[ 8 ], Giammanco, A[, 8, 191, ], Hollar, J[ 8 ], Jafari, A[ 8 ], Jez, P[ 8 ], Komm, M[ 8 ], Lemaitre, V[ 8 ], Nuttens, C[ 8 ], Pagano, D[ 8 ], Perrini, L[ 8 ], Pin, A[ 8 ], Piotrzkowski, K[ 8 ], Popov, 192, ], Quertenmont, L[ 8 ], Selvaggi, M[ 8 ], Marono, MV[ 8 ], Garcia, JMV[ 8 ], Beliy, N[ 9 ], Caebergs, T[ 9 ], Daubie, E[ 9 ], Hammad, GH[ 9 ], Alda, WL[ 10 ], Alves, GA[ 10 ], Brito, L[ 10 ], Martins, MC[ 10 ], Martins, TR[ 10 ], Herrera, CM[ 10 ], Pol, ME[ 10 ], Carvalho, W[ 11 ], Chinellato, J[ 11 ], Custodio, A[ 11 ], Da Costa, EM[ 11 ], Damiao, DD[ 11 ], Martins, CD[ 11 ], De Souza, SF[ 11 ], Malbouisson, H[ 11 ], Figueiredo, DM[ 11 ], Mundim, L[ 11 ], Nogima, H[ 11 ], Da Silva, WLP[ 11 ], Santaolalla, J[ 11 ], Santoro, A[ 11 ], Sznajder, A[ 11 ], Manganote, EJT[ 11 ], Pereira, AV[ 11 ], Bernardes, CA[ 13 ], Dogra, S[ 12 ], Tomei, TRFP[ 12 ], Gregores, EM[ 13 ], Mercadante, PG[ 13 ], Novaes, SF[ 12 ], Padula, SS[ 12 ], Aleksandrov, A[, 14, 81, ], Genchev, V[, 14, 189, ], Iaydjiev, P[ 14 ], Marinov, A[ 14 ], Piperov, S[ 14 ], Rodozov, M[ 14 ], Stoykova, S[ 14 ], Sultanov, G[ 14 ], Tcholakov, V[ 14 ], Vutova, M[ 14 ], Dimitrov, A[ 15 ], Glushkov, I[ 15 ], Hadjiiska, R[ 15 ], Kozhuharov, V[ 15 ], Litov, L[ 15 ], Pavlov, B[ 15 ], Petkov, P[ 15 ], Bian, JG[ 16 ], Chen, GM[ 16 ], Chen, HS[ 16 ], Chen, M[ 16 ], R[ 16 ], Du, Jiang, CH[ 16 ], Plestina, R[, 16, 194, ], Tao, J[ 16 ], Wang, Z[ 16 ], Asawatangtrakuldee, C[ 17 ], Ban, Y[ 17 ], Liu, S[ 17 ], Mao, Y[, 17, 184, ], Qian, Sj[, 17, 18, ], Wang, D[ 17 ], Zhang, L[ 17 ], Zou, W[ 17 ], Avila, C[ 18 ], Sierra, LFC[ 18 ], Florez, C[ 18 ], Gomez, JP[ 18 ], Moreno, BG[ 18 ], Sanabria, JC[ 18 ], Godinovic, N[ 19 ], Lelas, D[ 19 ], Polic, D[ 19 ], Puljak, I[ 19 ], Antunovic, Z[ 20 ], Kovac, M[ 20 ], Brigljevic, V[ 21 ], Kadija, K[ 21 ], Luetic, J[ 21 ], Mekterovic, D[ 21 ], Sudic, L[ 21 ], Attikis, A[ 22 ], Mavromanolakis, G[ 22 ], Mousa, J[ 22 ], Nicolaou, C[ 22 ], Ptochos, F[ 22 ], Razis, PA[ 22 ], Bodlak, M[ 23 ], Finger, M[ 23 ], Finger, M[, 23, 195, ], Assran, Y[, 24, 196, ], Kamel, Ae[, 24, 197, ], Mahmoud, Ma[, 24, 198, ], Radi, A[, 24, 199, ], Kadastik, M[ 25 ], Murumaa, M[ 25 ], Raidal, M[ 25 ], Tiko, A[ 25 ], Eerola, P[ 26 ], Fedi, G[ 26 ], Voutilainen, M[ 26 ], Harkonen, J[ 27 ], Karimaki, V[ 27 ], Kinnunen, R[ 27 ], Kortelainen, MJ[ 27 ], Lampen, T[ 27 ], Lassila Perini, K[ 27 ], Lehti, S[ 27 ], Linden, T[ 27 ], Luukka, P[ 27 ], Maenpaa, T[ 27 ], Peltola, T[ 27 ], Tuominen, E[ 27 ], Tuominiemi, J[ 27 ], Tuovinen, E[ 27 ], Wendland, L[ 27 ], Talvitie, J[ 28 ], Tuuva, T[ 28 ], Besancon, M[ 29 ], Couderc, F[ 29 ], Dejardin, M[ 29 ], Denegri, D[ 29 ], Fabbro, B[ 29 ], Faure, JL[ 29 ], Favaro, C[ 29 ], Ferri, F[ 29 ], Ganjour, S[ 29 ], Givernaud, A[ 29 ], Gras, P[ 29 ], de Monchenault, GH[ 29 ], Jarry, P[ 29 ], Locci, E[ 29 ], Malcles, J[ 29 ], Rander, J[ 29 ], Rosowsky, A[ 29 ], Titov, M[ 29 ], Baffioni, S[ 30 ], Beaudette, F[ 30 ], Busson, P[ 30 ], Charlot, C[ 30 ], Dahms, T[ 30 ], Dalchenko, M[ 30 ], Dobrzynski, L[ 30 ], Filipovic, N[ 30 ], Florent, A[ 30 ], de Cassagnac, RG[ 30 ], Mastrolorenzo, L[ 30 ], Mine, P[ 30 ], Mironov, C[ 30 ], Naranjo, IN[ 30 ], Nguyen, M[ 30 ], Ochando, C[ 30 ], Paganini, P[ 30 ], Regnard, S[ 30 ], Salerno, R[ 30 ], Sauvan, JB[ 30 ], Sirois, Y[ 30 ], Veelken, C[ 30 ], Yilmaz, Y[ 30 ], Zabi, A[ 30 ], Agram, Jl[, 31, 200, ], Andrea, J[ 31 ], Aubin, A[ 31 ], Bloch, D[ 31 ], Brom, JM[ 31 ], Chabert, EC[ 31 ], Collard, C[ 31 ], Conte, E[, 31, Fontaine, Jc[, 31, Gele, D[ 31 ], Goerlach, U[ 31 ], Goetzmann, C[ 31 ], Le Bihan, AC[ 31 ], Van Hove, P[ 31 ], Gadrat, S[ 32 ], Beauceron, S[ 33 ], Beaupere, N[ 33 ], Boudoul, G[, 33, Bouvier, E[ 33 ], Brochet, S[ 33 ], Montoya, CAC[ 33 ], Chasserat, J[ 33 ], Chierici, R[ 33 ], Contardo, D[, 33, Depasse, P[ 33 ], El Mamouni, H[ 33 ], Fan, J[ 33 ], Fay, J[ 33 ], Gascon, S[ 33 ], Gouzevitch, M[ 33 ], Ille, B[ 33 ], Kurca, T[ 33 ], Lethuillier, M[ 33 ], Mirabito, L[ 33 ], Perries, S[ 33 ], Alvarez, JDR[ 33 ], Sabes, D[ 33 ], Sgandurra, L[ 33 ], Sordini, V[ 33 ], Donckt, MV[ 33 ], Verdier, P[ 33 ], Viret, S[ 33 ], Xiao, H[ 33 ], Tsamalaidze, Z[, 34, Autermann, C[ 35 ], Beranek, S[ 35 ], Bontenackels, M[ 35 ], Edelhoff, M[ 35 ], Feld, L[ 35 ], Hindrichs, O[ 35 ], Klein, K[ 35 ], Ostapchuk, A[ 35 ], Perieanu, A[ 35 ], Raupach, F[ 35 ], Sammet, J[ 35 ], Schael, S[ 35 ], Weber, H[ 35 ], Wittmer, B[ 35 ], Zhukov, V[, 35, Ata, M[ 36 ], Brodski, M[ 36 ], Dietz Laursonn, E[ 36 ], Duchardt, D[ 36 ], Erdmann, M[ 36 ], Fischer, R[ 36 ], Guth, A[ 36 ], Hebbeker, T[ 36 ], Heidemann, C[ 36 ], Hoepfner, K[ 36 ], Klingebiel, D[ 36 ], Knutzen, S[ 36 ], Kreuzer, P[ 36 ], Merschmeyer, M[ 36 ], Meyer, A[ 36 ], Millet, P[ 36 ], Olschewski, M[ 36 ], Padeken, K[ 36 ], Papacz, P[ 36 ], Reithler, H[ 36 ], Schmitz, SA[ 36 ], Sonnenschein, L[ 36 ], Teyssier, D[ 36 ], Thuer, S[ 36 ], Weber, M[, 36, 144, ], Cherepanov, V[ 37 ], Erdogan, Y[ 37 ], Flugge, G[ 37 ], Geenen, H[ 37 ], Geisler, M[ 37 ], Ahmad, WH[ 37 ], Heister, A[ 37 ], Hoehle, F[ 37 ], Kargoll, B[ 37 ], Kress, T[ 37 ], Kuessel, Y[ 37 ], Kunsken, A[ 37 ], Lingemann, J[ 37 ], Nowack, A[ 37 ], Nugent, IM[ 37 ], Perchalla, L[ 37 ], Pooth, O[ 37 ], Stahl, A[ 37 ], Asin, I[ 38 ], Bartosik, N[ 38 ], Behr, J[ 38 ], Behrenhoff, W[ 38 ], Behrens, U[ 38 ], Bell, AJ[ 38 ], Bergholz, M[, 38, 201, ], Bethani, A[ 38 ], Borras, K[ 38 ], Burgmeier, A[ 38 ], Cakir, A[ 38 ], Calligaris, L[ 38 ], Campbell, A[ 38 ], Choudhury, S[ 38 ], Costanza, F[ 38 ], Pardos, CD[ 38 ], Dooling, S[ 38 ], Dorland, T[ 38 ], Eckerlin, G[ 38 ], Eckstein, D[ 38 ], Eichhorn, T[ 38 ], Flucke, G[ 38 ], Garcia, JG[ 38 ], Geiser, A[ 38 ], Gunnellini, P[ 38 ], Hauk, J[ 38 ], Hempel, Horton, D[ 38 ], Jung, H[ 38 ], Kalogeropoulos, A[ 38 ], Kasemann, M[ 38 ], Katsas, P[ 38 ], Kieseler, J[ 38 ], Kleinwort, C[ 38 ], Krucker, D[ 38 ], Lange, W[ 38 ], Leonard, J[ 38 ], Lipka, K[ 38 ], Lobanov, A[ 38 ], Lohmann, W[, 38, Lutz, B[ 38 ], Mankel, R[ 38 ], Marfin, I[, 38, Melzer Pellmann, IA[ 38 ], Meyer, AB[ 38 ], Mittag, G[ 38 ], Mnich, J[ 38 ], Mussgiller, A[ 38 ], Naumann Emme, S[ 38 ], Nayak, A[ 38 ], Novgorodova, O[ 38 ], Ntomari, E[ 38 ], Perrey, H[ 38 ], Pitzl, D[ 38 ], Placakyte, R[ 38 ], Raspereza, A[ 38 ], Cipriano, PMR[ 38 ], Roland, B[ 38 ], Ron, E[ 38 ], Sahin, MO[ 38 ], Salfeld Nebgen, J[ 38 ], Saxena, P[ 38 ], Schmidt, R[, 38, Schoerner Sadenius, T[ 38 ], Schroder, M[ 38 ], Seitz, C[ 38 ], Spannagel, S[ 38 ], Trevino, ADRV[ 38 ], Walsh, R[ 38 ], Wissing, C[ 38 ], Martin, MA[ 39 ], Blobel, V[ 39 ], Vignali, MC[ 39 ], Draeger, AR[ 39 ], Erfle, J[ 39 ], Garutti, E[ 39 ], Goebel, K[ 39 ], Gorner, M[ 39 ], Haller, J[ 39 ], Hoffmann, M[ 39 ], Hoing, RS[ 39 ], Kirschenmann, H[ 39 ], Klanner, R[ 39 ], Kogler, R[ 39 ], Lange, J[ 39 ], Lapsien, T[ 39 ], Lenz, T[ 39 ], Marchesini, I[ 39 ], Ott, J[ 39 ], Peiffer, T[ 39 ], Pietsch, N[ 39 ], Poehlsen, J[ 39 ], Poehlsen, T[ 39 ], Rathjens, D[ 39 ], Sander, C[ 39 ], Schettler, H[ 39 ], Schleper, P[ 39 ], Schlieckau, E[ 39 ], Schmidt, A[ 39 ], Seidel, M[ 39 ], Sola, V[ 39 ], Stadie, H[ 39 ], Steinbruck, G[ 39 ], Troendle, D[ 39 ], Usai, E[ 39 ], Vanelderen, L[ 39 ], Vanhoefer, A[ 39 ], Barth, C[ 40 ], Baus, C[ 40 ], Berger, J[ 40 ], Boser, C[ 40 ], Butz, E[ 40 ], Chwalek, T[ 40 ], De Boer, W[ 40 ], Descroix, A[ 40 ], Dierlamm, A[ 40 ], Feindt, M[ 40 ], Frensch, F[ 40 ], Giffels, M[ 40 ], Hartmann, F[, 40, Hauth, T[, 40, Husemann, U[ 40 ], Katkov, I[, 40, Kornmayer, A[, 40, Kuznetsova, E[ 40 ], Pardo, PL[ 40 ], Mozer, MU[ 40 ], Muller, T[ 40 ], Nurnberg, A[ 40 ], Quast, G[ 40 ], Rabbertz, K[ 40 ], Ratnikov, F[ 40 ], Rocker, S[ 40 ], Simonis, HJ[ 40 ], Stober, FM[ 40 ], Ulrich, R[ 40 ], Wagner Kuhr, J[ 40 ], Wayand, S[ 40 ], Weiler, T[ 40 ], Wolf, R[ 40 ], Anagnostou, G[ 41 ], Daskalakis, G[ 41 ], Geralis, T[ 41 ], Giakoumopoulou, VA[ 41 ], Kyriakis, A[ 41 ], Loukas, D[ 41 ], Markou, A[ 41 ], Markou, C[ 41 ], Psallidas, A[ 41 ], Topsis Giotis, I[ 41 ], Kesisoglou, S[ 42 ], Panagiotou, A[ 42 ], Saoulidou, N[ 42 ], Stiliaris, E[ 42 ], Aslanoglou, X[ 43 ], Evangelou, I[ 43 ], Flouris, G[ 43 ], Foudas, C[ 43 ], Kokkas, P[ 43 ], Manthos, N[ 43 ], Papadopoulos, I[ 43 ], Paradas, E[ 43 ], Bencze, G[ 44 ], Hajdu, C[ 44 ], Hidas, P[ 44 ], Horvath, D[, 44, 202, ], Sikler, F[ 44 ], Veszpremi, V[ 44 ], Vesztergombi, G[, 44, 203, ], Zsigmond, AJ[ 44 ], Beni, N[ 45 ], Czellar, S[ 45 ], Karancsi, J[, 45, 204, ], Molnar, J[ 45 ], Palinkas, J[ 45 ], Szillasi, Z[ 45 ], Raics, P[ 46 ], Trocsanyi, ZL[ 46 ], Ujvari, B[ 46 ], Swain, SK[ 47 ], Beri, SB[ 48 ], Bhatnagar, V[ 48 ], Gupta, R[ 48 ], Bhawandeep, U[ 48 ], Kalsi, AK[ 48 ], Kaur, M[ 48 ], Kumar, R[ 48 ], Mittal, M[ 48 ], Nishu, N[ 48 ], Singh, JB[ 48 ], Kumar, A[ 49 ], Ahuja, S[ 49 ], Bhardwaj, A[ 49 ], Choudhary, BC[ 49 ], Kumar, A[, 49, 168, ], Malhotra, S[ 49 ], Naimuddin, M[ 49 ], Ranjan, K[ 49 ], Sharma, V[, 49, 145, ], Banerjee, S[, 50, 52, ], Bhattacharya, 142, ], Chatterjee, K[ 50 ], Dutta, S[ 50 ], Gomber, B[ 50 ], Jain, S[ 50 ], Khurana, R[ 50 ], Modak, A[ 50 ], Mukherjee, S[ 50 ], Roy, D[ 50 ], Sarkar, S[ 50 ], Sharan, M[ 50 ], Abdulsalam, A[ 51 ], Dutta, D[ 51 ], Kailas, S[ 51 ], Kumar, V[ 51 ], Mohanty, Ak[, 51, Pant, LM[ 51 ], Shukla, P[ 51 ], Topkar, A[ 51 ], Aziz, T[ 52 ], Banerjee, S, Bhowmik, S[, 52, 205, ], Chatterjee, RM[ 52 ], Dewanjee, RK[ 52 ], Dugad, S[ 52 ], Ganguly, S[ 52 ], Ghosh, S[ 52 ], Guchait, M[ 52 ], Gurtu, A[ 52 ], Kole, G[ 52 ], Kumar, S[ 52 ], Maity, M[, 52, Majumder, G[ 52 ], Mazumdar, K[ 52 ], Mohanty, GB[ 52 ], Parida, B[ 52 ], Sudhakar, K[ 52 ], Wickramage, N[, 52, 206, ], Bakhshiansohi, H[ 53 ], Behnamian, H[ 53 ], Etesami, Sm[, 53, 207, ], Fahim, A[, 53, 208, ], Goldouzian, R[ 53 ], Khakzad, M[ 53 ], Najafabadi, MM[ 53 ], Naseri, M[ 53 ], Mehdiabadi, SP[ 53 ], Hosseinabadi, FR[ 53 ], Safarzadeh, B[, 53, 209, ], Zeinali, M[ 53 ], Felcini, M[ 54 ], Grunewald, M[ 54 ], Abbrescia, M[, 55, 56, ], Barbone, L[, 55, Calabria, C[, 55, Chhibra, Ss[, 55, Colaleo, A[ 55 ], Creanza, D[, 55, 57, ], Filippis, De, N[, 55, Palma, De, Fiore, L[ 55 ], Iaselli, G[, 55, Maggi, Maggi, M[ 55 ], S[, 55, Nuzzo, Pompili, A[, 55, Pugliese, Radogna, R[, 55, Selvaggi, Silvestris, Singh, Venditti, Zito, G[ 55 ], Abbiendi, G[ 58 ], Benvenuti, AC[ 58 ], Bonacorsi, D[, 58, 59, ], Braibant, Giacomelli, S[, 58, Brigliadori, L[, 58, Campanini, R[, 58, Capiluppi, P[, 58, Castro, A[, 58, Cavallo, R[ 58 ], Codispoti, G[, 58, Cuffiani, M[, 58, Dallavalle, GM[ 58 ], Fabbri, F[ 58 ], Fanfani, Fasanella, Giacomelli, P[ 58 ], Grandi, C[ 58 ], Guiducci, Marcellini, S[ 58 ], Masetti, G[ 58 ], Montanari, A[ 58 ], Navarria, Fl[, 58, Perrotta, A[ 58 ], Primavera, F[, 58, Rossi, Am[, 58, Rovelli, T[, 58, Siroli, Gp[, 58, Tosi, N[, 58, Travaglini, Albergo, S[, 60, 61, ], Cappello, G[ 60 ], Chiorboli, M[, 60, Costa, Giordano, F[, 60, Potenza, R[, 60, Tricomi, A[, 60, Tuve, C[, 60, Barbagli, G[ 63 ], Ciulli, V[, 63, 64, ], Civinini, C[ 63 ], D'Alessandro, R[, 63, Focardi, E[, 63, Gallo, E[ 63 ], Gonzi, S[, 63, Gori, Lenzi, P[, 63, Meschini, M[ 63 ], Paoletti, S[ 63 ], Sguazzoni, G[ 63 ], Tropiano, A[, 63, Benussi, L[ 65 ], Bianco, S[ 65 ], Fabbri, F[ 65 ], Piccolo, D[ 65 ], Ferretti, Roberta, Ferro, F[ 66 ], LO VETERE, Maurizio, Robutti, E[ 66 ], Tosi, Silvano, Dinardo, Me[, 68, 69, ], Fiorendi, S[, 68, Gennai, Gerosa, R[ 189 ], Ghezzi, A[, 68, Govoni, P[, 68, Lucchini, Mt[, 68, Malvezzi, S[ 68 ], Manzoni, Ra[, 68, Martelli, Marzocchi, B, Menasce, D[ 68 ], Moroni, L[ 68 ], Paganoni, M[, 68, Pedrini, D[ 68 ], Ragazzi, Redaelli, N[ 68 ], Fatis, De, Tt[, 68, Buontempo, S[ 70 ], Cavallo, N[, 70, 72, ], Guida, Di, S[, 70, Fabozzi, F[, 70, Iorio, Aom[, 70, 71, ], Lista, L[ 70 ], Meola, Merola, M[ 70 ], Paolucci, P[, 70, Azzi, P[ 74 ], Bacchetta, N[ 74 ], Bellato, M[ 74 ], Biasotto, M[, 74, 210, ], Branca, A[, 74, 75, ], Carlin, R[, 74, Checchia, P[ 74 ], Dall'Osso, Dorigo, T[ 74 ], Fanzago, F[ 74 ], Galanti, Gasparini, F[, 74, U[, 74, Giubilato, P[, 74, Gozzelino, A[ 74 ], Kanishchev, K[, 74, 76, ], Lacaprara, S[ 74 ], Margoni, Meneguzzo, At[, 74, Pazzini, J[, 74, Pozzobon, N[, 74, Ronchese, Simonetto, Torassa, E[ 74 ], Zotto, Zucchetta, Gabusi, M[, 77, 78, ], Ratti, Sp[, 77, V[ 77 ], Re, Riccardi, C[, 77, Salvini, P[ 77 ], Vitulo, P[, 77, Biasini, M[, 79, 80, ], Bilei, GM[ 79 ], Ciangottini, D[, 79, Fano, L[, 79, Lariccia, P[, 79, Mantovani, G[, 79, Menichelli, M[ 79 ], Romeo, F[, 79, Saha, A[ 79 ], Santocchia, A[, 79, Spiezia, Androsov, K[ 211 ], Azzurri, P[ 81 ], Bagliesi, G[ 81 ], Bernardini, J[ 81 ], Boccali, T[ 81 ], Broccolo, G[, 81, 83, ], Castaldi, R[ 81 ], Ciocci, Ma[, 81, 211, ], Dell'Orso, R[ 81 ], Donato, S[, 81, Fiori, F[, 81, Foa, L[, 81, Giassi, A[ 81 ], Grippo, Mt[, 81, Ligabue, Lomtadze, T[ 81 ], Martini, 82, ], Messineo, A[, 81, Moon, Cs[, 81, 212, ], Palla, Rizzi, Savoy, Navarro, 213, ], Serban, AT[ 81 ], Spagnolo, P[ 81 ], Squillacioti, P[, 81, Tenchini, R[ 81 ], Tonelli, Venturi, A[ 81 ], Verdini, PG[ 81 ], Vernieri, C[, 81, Barone, L[, 84, 85, ], Cavallari, F[ 84 ], 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92 ], Kim, MS[ 92 ], Kong, DJ[ 92 ], Lee, S[ 92 ], YD[ 92 ], Oh, Park, H[ 92 ], Sakharov, A[ 92 ], Son, DC[ 92 ], Kim, TJ[ 93 ], Kim, JY[ 94 ], Song, S[ 94 ], Choi, S[ 95 ], Gyun, D[ 95 ], Hong, B[ 95 ], M[ 95 ], Jo, Kim, H[ 95 ], Kim, Y[ 95 ], Lee, B[ 95 ], Lee, KS[ 95 ], Park, SK[ 95 ], Roh, Y[ 95 ], Choi, M[ 96 ], Kim, JH[ 96 ], Park, IC[ 96 ], Ryu, G[ 96 ], Ryu, MS[ 96 ], Choi, Y[ 97 ], Choi, YK[ 97 ], Goh, J[ 97 ], Kim, D[ 97 ], Kwon, E[ 97 ], Lee, J[ 97 ], Seo, H[ 97 ], I[ 97 ], Yu, Juodagalvis, A[ 98 ], Komaragiri, JR[ 99 ], Ali, MABM[ 99 ], Castilla Valdez, H[ 100 ], De La Cruz Burelo, E[ 100 ], Heredia de La Cruz, I[ 100 ], Hernandez Almada, A[ 100 ], Lopez Fernandez, R[ 100 ], Sanchez Hernandez, A[ 100 ], Moreno, SC[ 101 ], Valencia, FV[ 101 ], Pedraza, I[ 102 ], Ibarguen, HAS[ 102 ], Linares, EC[ 103 ], Pineda, AM[ 103 ], Krofcheck, D[ 104 ], Butler, PH[ 105 ], Reucroft, S[ 105 ], Ahmad, A[ 106 ], Ahmad, M[ 106 ], Hassan, Q[ 106 ], Hoorani, HR[ 106 ], Khalid, S[ 106 ], Khan, WA[ 106 ], Khurshid, T[ 106 ], Shah, MA[ 106 ], Shoaib, M[ 106 ], Bialkowska, H[ 107 ], Bluj, M[ 107 ], Boimska, B[ 107 ], Frueboes, T[ 107 ], Gorski, M[ 107 ], Kazana, M[ 107 ], Nawrocki, K[ 107 ], Romanowska Rybinska, K[ 107 ], Szleper, M[ 107 ], Zalewski, P[ 107 ], Brona, G[ 108 ], Bunkowski, K[ 108 ], Cwiok, M[ 108 ], Dominik, W[ 108 ], Doroba, K[ 108 ], Kalinowski, A[ 108 ], Konecki, M[ 108 ], Krolikowski, J[ 108 ], Misiura, M[ 108 ], Olszewski, M[ 108 ], Wolszczak, W[ 108 ], Bargassa, P[ 109 ], Silva, CBDE[ 109 ], Faccioli, P[ 109 ], Parracho, PGF[ 109 ], Gallinaro, M[ 109 ], Iglesias, LL[ 109 ], Nguyen, F[ 109 ], Antunes, JR[ 109 ], Seixas, J[ 109 ], Varela, J[ 109 ], Vischia, P[ 109 ], Afanasiev, S[ 110 ], Bunin, P[ 110 ], Gavrilenko, M[ 110 ], Golutvin, I[ 110 ], Gorbunov, I[ 110 ], Kamenev, A[ 110 ], Karjavin, V[ 110 ], Konoplyanikov, V[ 110 ], Lanev, A[ 110 ], Malakhov, A[ 110 ], Matveev, V[ 110 ], Moisenz, P[ 110 ], Palichik, V[ 110 ], Perelygin, V[ 110 ], Shmatov, S[ 110 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Duric, S., Friis, E., Hall-Wilton, R., Herndon, M., Hervé, A., Klabbers, P., Lanaro, A., Lazaridis, C., Levine, A., Loveless, R., Mohapatra, A., Ojalvo, I., Perry, T., Pierro, G.A., Polese, G., Ross, I., Sarangi, T., Savin, A., Smith, W.H., Taylor, D., Verwilligen, P., Vuosalo, C., Woods, N., Institut de Recherches sur les lois Fondamentales de l'Univers (IRFU), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Paris-Saclay, Laboratoire Leprince-Ringuet (LLR), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-École polytechnique (X)-Centre National de la Recherche Scientifique (CNRS), Institut Pluridisciplinaire Hubert Curien (IPHC), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Centre de Calcul de l'IN2P3 (CC-IN2P3), Centre National de la Recherche Scientifique (CNRS)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Institut de Physique Nucléaire de Lyon (IPNL), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), CMS, Centre National de la Recherche Scientifique (CNRS)-École polytechnique (X)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Université de Strasbourg (UNISTRA)-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de Physique Nucléaire et de Physique des Particules du CNRS (IN2P3), Physics, Elementary Particle Physics, Khachatryan, V, 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Departamento de Física Teórica, Karapınar, Güler, İYTE, Fen Fakültesi, Matematik Bölümü, UCL - SST/IRMP - Institut de recherche en mathématique et physique, UNIVERSIDADE DE ESTADUAL DE CAMPINAS, Khachatryan, V. A, Sirunyan, A. M. A, Tumasyan, A. A, Adam, W. B, Bergauer, T. B, Dragicevic, M. B, Erö, J. B, Fabjan, C. B, Friedl, M. B, Frühwirth, R. B, Ghete, V. M. B, Hartl, C. B, Hörmann, N. B, Hrubec, J. B, Jeitler, M. B, Kiesenhofer, W. B, Knünz, V. B, Krammer, M. B, Krätschmer, I. B, Liko, D. B, Mikulec, I. B, Rabady, D. B, Rahbaran, B. B, Rohringer, H. B, Schöfbeck, R. B, Strauss, J. B, Taurok, A. B, Treberer Treberspurg, W. B, Waltenberger, W. B, Wulz, C. E. b, Mossolov, V. C, Shumeiko, N. C, Suarez Gonzalez, J. C, Alderweireldt, S. D, Bansal, M. D, Bansal, S. D, Cornelis, T. D, De Wolf, E. A. D, Janssen, X. D, Knutsson, A. D, Luyckx, S. D, Ochesanu, S. D, Roland, B. D, Rougny, R. D, Van De Klundert, M. D, Van Haevermaet, H. D, Van Mechelen, P. D, Van Remortel, N. D, Van Spilbeeck, A. D, Blekman, F. E, Blyweert, S. E, D’Hondt, J. E, Daci, N. E, Heracleous, N. E, Keaveney, J. E, Lowette, S. E, Maes, M. E, Olbrechts, A. E, Python, Q. E, Strom, D. E, Tavernier, S. E, Van Doninck, W. E, Van Mulders, P. E, Van Onsem, G. P. E, Villella, I. E, Caillol, C. F, Clerbaux, B. F, De Lentdecker, G. F, Dobur, D. F, Favart, L. F, Gay, A. P. R. F, Grebenyuk, A. F, Léonard, A. F, Mohammadi, A. F, Perniè, L. F, Reis, T. F, Seva, T. F, Thomas, L. F, Vander Velde, C. F, Vanlaer, P. F, Wang, J. F, Adler, V. G, Beernaert, K. G, Benucci, L. G, Cimmino, A. G, Costantini, S. G, Crucy, S. G, Dildick, S. G, Fagot, A. G, Garcia, G. G, Mccartin, J. G, Ocampo Rios, A. A. G, Ryckbosch, D. G, Salva Diblen, S. G, Sigamani, M. G, Strobbe, N. G, Thyssen, F. G, Tytgat, M. G, Yazgan, E. G, Zaganidis, N. G, Basegmez, S. H, Beluffi, C. H, Bruno, G. H, Castello, R. H, Caudron, A. H, Ceard, L. H, Da Silveira, G. G. H, Delaere, C. H, du Pree, T. H, Favart, D. H, Forthomme, L. H, Giammanco, A. H, Hollar, J. H, Jez, P. H, Komm, M. H, Lemaitre, V. H, Nuttens, C. H, Pagano, D. H, Perrini, L. H, Pin, A. H, Piotrzkowski, K. H, Popov, A. H, Quertenmont, L. H, Selvaggi, M. H, Vidal Marono, M. H, Vizan Garcia, J. M. H, Beliy, N. I, Caebergs, T. I, Daubie, E. I, Hammad, G. H. I, Júnior, W. L. A. I, Alves, G. A. J, Brito, L. J, Correa Martins Junior, M. J, Martins, T. D. R. J, Herrera, C. M. J, Pol, M. E. J, Carvalho, W. K, Chinellato, J. K, Custódio, A. K, Da Costa, E. M. K, De Jesus Damiao, D. K, De Oliveira Martins, C. K, Fonseca De Souza, S. K, Malbouisson, H. K, Matos Figueiredo, D. K, Mundim, L. K, Nogima, H. K, Prado Da Silva, W. L. K, Santaolalla, J. K, Santoro, A. K, Sznajder, A. K, Tonelli Manganote, E. J. K, Vilela Pereira, A. K, Bernardes, C. A. L, Dogra, S. L, Fernandez Perez Tomei, T. R. L, Gregores, E. M. L, Mercadante, P. G. L, Novaes, S. F. L, Padula, S. S. L, Aleksandrov, A. M, Genchev, V. M, Iaydjiev, P. M, Marinov, A. M, Piperov, S. M, Rodozov, M. M, Stoykova, S. M, Sultanov, G. M, Tcholakov, V. M, Vutova, M. M, Dimitrov, A. N, Glushkov, I. N, Hadjiiska, R. N, Kozhuharov, V. N, Litov, L. N, Pavlov, B. N, Petkov, P. N, Bian, J. G. O, Chen, G. M. O, Chen, H. S. O, Chen, M. O, Du, R. O, Jiang, C. H. O, Liang, S. O, Plestina, R. O, Tao, J. O, Wang, X. O, Wang, Z. O, Asawatangtrakuldee, C. P, Ban, Y. P, Guo, Y. P, Li, Q. P, Li, W. P, Liu, S. P, Mao, Y. P, Qian, S. J. P, Wang, D. P, Zhang, L. P, Zou, W. P, Avila, C. Q, Chaparro Sierra, L. F. Q, Florez, C. Q, Gomez, J. P. Q, Gomez Moreno, B. Q, Sanabria, J. C. Q, Godinovic, N. R, Lelas, D. R, Polic, D. R, Puljak, I. R, Antunovic, Z. S, Kovac, M. S, Brigljevic, V. T, Kadija, K. T, Luetic, J. T, Mekterovic, D. T, Sudic, L. T, Attikis, A. U, Mavromanolakis, G. U, Mousa, J. U, Nicolaou, C. U, Ptochos, F. U, Razis, P. A. U, Bodlak, M. V, Finger, M. V, Assran, Y. W, Kamel, A. E. W, Mahmoud, M. A. W, Radi, A. W, Kadastik, M. X, Murumaa, M. X, Raidal, M. X, Tiko, A. X, Eerola, P. Y, Fedi, G. Y, Voutilainen, M. Y, Härkönen, J. Z, Karimäki, V. Z, Kinnunen, R. Z, Kortelainen, M. J. Z, Lampén, T. Z, Lassila Perini, K. Z, Lehti, S. Z, Lindén, T. Z, Luukka, P. Z, Mäenpää, T. Z, Peltola, T. Z, Tuominen, E. Z, Tuominiemi, J. Z, Tuovinen, E. Z, Wendland, L. Z, Talvitie, J. Aa, Tuuva, T. Aa, Besancon, M. Ab, Couderc, F. Ab, Dejardin, M. Ab, Denegri, D. Ab, Fabbro, B. Ab, Faure, J. L. Ab, Favaro, C. Ab, Ferri, F. Ab, Ganjour, S. Ab, Givernaud, A. Ab, Gras, P. Ab, Hamel de Monchenault, G. Ab, Jarry, P. Ab, Locci, E. Ab, Malcles, J. Ab, Rander, J. Ab, Rosowsky, A. Ab, Titov, M. Ab, Baffioni, S. Ac, Beaudette, F. Ac, Busson, P. Ac, Charlot, C. Ac, Dahms, T. Ac, Dalchenko, M. Ac, Dobrzynski, L. Ac, Filipovic, N. Ac, Florent, A. Ac, Granier de Cassagnac, R. Ac, Mastrolorenzo, L. Ac, Miné, P. Ac, Mironov, C. Ac, Naranjo, I. N. Ac, Nguyen, M. Ac, Ochando, C. Ac, Paganini, P. Ac, Regnard, S. Ac, Salerno, R. Ac, Sauvan, J. B. Ac, Sirois, Y. Ac, Veelken, C. Ac, Yilmaz, Y. Ac, Zabi, A. Ac, Agram, J. L. ad, Andrea, J. Ad, Aubin, A. Ad, Bloch, D. Ad, Brom, J. M. ad, Chabert, E. C. Ad, Collard, C. Ad, Conte, E. Ad, Fontaine, J. C. ad, Gelé, D. Ad, Goerlach, U. Ad, Goetzmann, C. Ad, Le Bihan, A. C. ad, Van Hove, P. Ad, Gadrat, S. Ae, Beauceron, S. Af, Beaupere, N. Af, Boudoul, G. Af, Bouvier, E. Af, Brochet, S. Af, Carrillo Montoya, C. A. Af, Chasserat, J. Af, Chierici, R. Af, Contardo, D. Af, Depasse, P. Af, El Mamouni, H. Af, Fan, J. Af, Fay, J. Af, Gascon, S. Af, Gouzevitch, M. Af, Ille, B. Af, Kurca, T. Af, Lethuillier, M. Af, Mirabito, L. Af, Perries, S. Af, Ruiz Alvarez, J. D. Af, Sabes, D. Af, Sgandurra, L. Af, Sordini, V. Af, Vander Donckt, M. Af, Verdier, P. Af, Viret, S. Af, Xiao, H. Af, Tsamalaidze, Z. Ag, Autermann, C. Ah, Beranek, S. Ah, Bontenackels, M. Ah, Edelhoff, M. Ah, Feld, L. Ah, Hindrichs, O. Ah, Klein, K. Ah, Ostapchuk, A. Ah, Perieanu, A. Ah, Raupach, F. Ah, Sammet, J. Ah, Schael, S. Ah, Weber, H. Ah, Wittmer, B. Ah, Zhukov, V. Ah, Ata, M. Ai, Brodski, M. Ai, Dietz Laursonn, E. Ai, Duchardt, D. Ai, Erdmann, M. Ai, Fischer, R. Ai, Güth, A. Ai, Hebbeker, T. Ai, Heidemann, C. Ai, Hoepfner, K. Ai, Klingebiel, D. Ai, Knutzen, S. Ai, Kreuzer, P. Ai, Merschmeyer, M. Ai, Meyer, A. Ai, Millet, P. Ai, Olschewski, M. Ai, Padeken, K. Ai, Papacz, P. Ai, Reithler, H. Ai, Schmitz, S. A. Ai, Sonnenschein, L. Ai, Teyssier, D. Ai, Thüer, S. Ai, Weber, M. Ai, Cherepanov, V. Aj, Erdogan, Y. Aj, Flügge, G. Aj, Geenen, H. Aj, Geisler, M. Aj, Haj Ahmad, W. Aj, Heister, A. Aj, Hoehle, F. Aj, Kargoll, B. Aj, Kress, T. Aj, Kuessel, Y. Aj, Lingemann, J. Aj, Nowack, A. Aj, Nugent, I. M. Aj, Perchalla, L. Aj, Pooth, O. Aj, Stahl, A. Aj, Asin, I. Ak, Bartosik, N. Ak, Behr, J. Ak, Behrenhoff, W. Ak, Behrens, U. Ak, Bell, A. J. Ak, Bergholz, M. Ak, Bethani, A. Ak, Borras, K. Ak, Burgmeier, A. Ak, Cakir, A. Ak, Calligaris, L. Ak, Campbell, A. Ak, Choudhury, S. Ak, Costanza, F. Ak, Diez Pardos, C. Ak, Dooling, S. Ak, Dorland, T. Ak, Eckerlin, G. 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Am, Anagnostou, G. An, Daskalakis, G. An, Geralis, T. An, Giakoumopoulou, V. A. An, Kyriakis, A. An, Loukas, D. An, Markou, A. An, Markou, C. An, Psallidas, A. An, Topsis Giotis, I. An, Panagiotou, A. Ao, Agapitos, A. Ao, Kesisoglou, S. Ao, Saoulidou, N. Ao, Stiliaris, E. Ao, Aslanoglou, X. Ap, Evangelou, I. Ap, Flouris, G. Ap, Foudas, C. Ap, Kokkas, P. Ap, Manthos, N. Ap, Papadopoulos, I. Ap, Paradas, E. Ap, Bencze, G. Aq, Hajdu, C. Aq, Hidas, P. Aq, Horvath, D. Aq, Sikler, F. Aq, Veszpremi, V. Aq, Vesztergombi, G. Aq, Zsigmond, A. J. Aq, Beni, N. Ar, Czellar, S. Ar, Karancsi, J. Ar, Molnar, J. Ar, Palinkas, J. Ar, Szillasi, Z. Ar, Raics, P. A, Trocsanyi, Z. L. A, Ujvari, B. A, Swain, S. K. At, Beri, S. B. Au, Bhatnagar, V. Au, Gupta, R. Au, Bhawandeep, U. Au, Kalsi, A. K. Au, Kaur, M. Au, Mittal, M. Au, Nishu, N. Au, Singh, J. B. Au, Kumar, A. Av, Ahuja, S. Av, Bhardwaj, A. Av, Choudhary, B. C. Av, Malhotra, S. Av, Naimuddin, M. Av, Ranjan, K. Av, Sharma, V. Av, Banerjee, S. 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Dw, Alexander, J. Dx, Chatterjee, A. Dx, Chu, J. Dx, Dittmer, S. Dx, Eggert, N. Dx, Mirman, N. Dx, Nicolas Kaufman, G. Dx, Patterson, J. R. Dx, Ryd, A. Dx, Salvati, E. Dx, Skinnari, L. Dx, Sun, W. Dx, Teo, W. D. Dx, Thom, J. Dx, Thompson, J. Dx, Tucker, J. Dx, Weng, Y. Dx, Winstrom, L. Dx, Wittich, P. Dx, Winn, D. Dy, Abdullin, S. Dz, Albrow, M. Dz, Anderson, J. Dz, Apollinari, G. Dz, Bauerdick, L. A. T. Dz, Beretvas, A. Dz, Berryhill, J. Dz, Bhat, P. C. Dz, Burkett, K. Dz, Butler, J. N. Dz, Cheung, H. W. K. Dz, Chlebana, F. Dz, Cihangir, S. Dz, Elvira, V. D. Dz, Fisk, I. Dz, Freeman, J. Dz, Gao, Y. Dz, Gottschalk, E. Dz, Gray, L. Dz, Green, D. Dz, Grünendahl, S. Dz, Gutsche, O. Dz, Hanlon, J. Dz, Hare, D. Dz, Harris, R. M. Dz, Hirschauer, J. Dz, Hooberman, B. Dz, Jindariani, S. Dz, Johnson, M. Dz, Joshi, U. Dz, Kaadze, K. Dz, Klima, B. Dz, Kreis, B. Dz, Kwan, S. Dz, Linacre, J. Dz, Lincoln, D. Dz, Lipton, R. Dz, Liu, T. Dz, Lykken, J. Dz, Maeshima, K. Dz, Marraffino, J. M. Dz, Martinez Outschoorn, V. I. Dz, Maruyama, S. Dz, Mason, D. Dz, Mcbride, P. Dz, Mishra, K. Dz, Mrenna, S. Dz, Musienko, Y. Dz, Nahn, S. Dz, Newman Holmes, C. Dz, O’Dell, V. Dz, Prokofyev, O. Dz, Sexton Kennedy, E. Dz, Sharma, S. Dz, Soha, A. Dz, Spalding, W. J. Dz, Spiegel, L. Dz, Taylor, L. Dz, Tkaczyk, S. Dz, Tran, N. V. Dz, Uplegger, L. Dz, Vaandering, E. W. Dz, Vidal, R. Dz, Whitbeck, A. Dz, Whitmore, J. Dz, Yang, F. Dz, Acosta, D. Ea, Avery, P. Ea, Bourilkov, D. Ea, Carver, M. Ea, Cheng, T. Ea, Curry, D. Ea, Das, S. Ea, De Gruttola, M. Ea, Di Giovanni, G. P. Ea, Field, R. D. Ea, Fisher, M. Ea, Furic, I. K. Ea, Hugon, J. Ea, Konigsberg, J. Ea, Korytov, A. Ea, Kypreos, T. Ea, Low, J. F. Ea, Matchev, K. Ea, Milenovic, P. Ea, Mitselmakher, G. Ea, Muniz, L. Ea, Rinkevicius, A. Ea, Shchutska, L. Ea, Snowball, M. Ea, Yelton, J. Ea, Zakaria, M. Ea, Hewamanage, S. Eb, Linn, S. Eb, Markowitz, P. Eb, Martinez, G. Eb, Rodriguez, J. L. Eb, Adams, T. Ec, Askew, A. Ec, Bochenek, J. Ec, Diamond, B. Ec, Haas, J. Ec, Hagopian, S. Ec, Hagopian, V. Ec, Johnson, K. F. Ec, Prosper, H. Ec, Veeraraghavan, V. Ec, Weinberg, M. Ec, Baarmand, M. M. Ed, Hohlmann, M. Ed, Kalakhety, H. Ed, Yumiceva, F. Ed, Adams, M. R. Ee, Apanasevich, L. Ee, Bazterra, V. E. Ee, Berry, D. Ee, Betts, R. R. Ee, Bucinskaite, I. Ee, Cavanaugh, R. Ee, Evdokimov, O. Ee, Gauthier, L. Ee, Gerber, C. E. Ee, Hofman, D. J. Ee, Khalatyan, S. Ee, Kurt, P. Ee, Moon, D. H. Ee, O’Brien, C. Ee, Silkworth, C. Ee, Turner, P. Ee, Varelas, N. Ee, Albayrak, E. A. Ef, Bilki, B. Ef, Clarida, W. Ef, Dilsiz, K. Ef, Duru, F. Ef, Haytmyradov, M. Ef, Merlo, J. P. ef, Mermerkaya, H. Ef, Mestvirishvili, A. Ef, Moeller, A. Ef, Nachtman, J. Ef, Ogul, H. Ef, Onel, Y. Ef, Ozok, F. Ef, Penzo, A. Ef, Rahmat, R. Ef, Sen, S. Ef, Tan, P. Ef, Tiras, E. Ef, Wetzel, J. Ef, Yetkin, T. Ef, Yi, K. Ef, Barnett, B. A. Eg, Blumenfeld, B. Eg, Bolognesi, S. Eg, Fehling, D. Eg, Gritsan, A. V. Eg, Maksimovic, P. Eg, Martin, C. Eg, Swartz, M. Eg, Baringer, P. Eh, Bean, A. Eh, Benelli, G. Eh, Bruner, C. Eh, Kenny, R. P., Malek, M. Eh, Murray, M. Eh, Noonan, D. Eh, Sanders, S. Eh, Sekaric, J. Eh, Stringer, R. Eh, Wang, Q. Eh, Wood, J. S. Eh, Barfuss, A. F. Ei, Chakaberia, I. Ei, Ivanov, A. Ei, Khalil, S. Ei, Makouski, M. Ei, Maravin, Y. Ei, Saini, L. K. Ei, Shrestha, S. Ei, Skhirtladze, N. Ei, Svintradze, I. Ei, Gronberg, J. Ej, Lange, D. Ej, Rebassoo, F. Ej, Wright, D. Ej, Baden, A. Ek, Belloni, A. Ek, Calvert, B. Ek, Eno, S. C. Ek, Gomez, J. A. Ek, Hadley, N. J. Ek, Kellogg, R. G. Ek, Kolberg, T. Ek, Lu, Y. Ek, Marionneau, M. Ek, Mignerey, A. C. Ek, Pedro, K. Ek, Skuja, A. Ek, Tonjes, M. B. Ek, Tonwar, S. C. Ek, Apyan, A. El, Barbieri, R. El, Bauer, G. El, Busza, W. El, Cali, I. A. El, Chan, M. El, Di Matteo, L. El, Dutta, V. El, Gomez Ceballos, G. El, Goncharov, M. El, Gulhan, D. El, Klute, M. El, Lai, Y. S. El, Lee, Y. J. el, Levin, A. El, Luckey, P. D. El, Ma, T. El, Paus, C. El, Ralph, D. El, Roland, C. El, Roland, G. El, Stephans, G. S. F. El, Stöckli, F. El, Sumorok, K. El, Velicanu, D. El, Veverka, J. El, Wyslouch, B. El, Yang, M. El, Yoon, A. S. El, Zanetti, M. El, Zhukova, V. El, Dahmes, B. Em, De Benedetti, A. Em, Gude, A. Em, Kao, S. C. Em, Klapoetke, K. Em, Kubota, Y. Em, Mans, J. Em, Pastika, N. Em, Rusack, R. Em, Singovsky, A. Em, Tambe, N. Em, Turkewitz, J. Em, Acosta, J. G. En, Cremaldi, L. M. En, Kroeger, R. En, Oliveros, S. En, Perera, L. En, Sanders, D. A. En, Summers, D. En, Avdeeva, E. Eo, Bloom, K. Eo, Bose, S. Eo, Claes, D. R. Eo, Dominguez, A. Eo, Gonzalez Suarez, R. Eo, Keller, J. Eo, Knowlton, D. Eo, Kravchenko, I. Eo, Lazo Flores, J. Eo, Malik, S. Eo, Meier, F. Eo, Snow, G. R. Eo, Dolen, J. Ep, Godshalk, A. Ep, Iashvili, I. Ep, Jain, S. Ep, Kharchilava, A. Ep, Kumar, A. Ep, Rappoccio, S. Ep, Alverson, G. Eq, Barberis, E. Eq, Baumgartel, D. Eq, Chasco, M. Eq, Haley, J. Eq, Massironi, A. Eq, Nash, D. Eq, Orimoto, T. Eq, Trocino, D. Eq, Wang, R. J. eq, Wood, D. Eq, Zhang, J. Eq, Anastassov, A. Er, Hahn, K. A. Er, Kubik, A. Er, Lusito, L. Er, Mucia, N. Er, Odell, N. Er, Pollack, B. Er, Pozdnyakov, A. Er, Schmitt, M. Er, Stoynev, S. Er, Sung, K. Er, Velasco, M. Er, Won, S. Er, Brinkerhoff, A. E, Chan, K. M. E, Drozdetskiy, A. E, Hildreth, M. E, Jessop, C. E, Karmgard, D. J. E, Kellams, N. E, Lannon, K. E, Luo, W. E, Lynch, S. E, Marinelli, N. E, Pearson, T. E, Planer, M. E, Ruchti, R. E, Valls, N. E, Wayne, M. E, Wolf, M. E, Woodard, A. E, Antonelli, L. Et, Brinson, J. Et, Bylsma, B. Et, Durkin, L. S. Et, Flowers, S. Et, Hill, C. Et, Hughes, R. Et, Kotov, K. Et, Ling, T. Y. Et, Puigh, D. Et, Rodenburg, M. Et, Smith, G. Et, Winer, B. L. Et, Wolfe, H. Et, Wulsin, H. W. Et, Driga, O. Eu, Elmer, P. Eu, Hebda, P. Eu, Hunt, A. Eu, Koay, S. A. Eu, Lujan, P. Eu, Marlow, D. Eu, Medvedeva, T. Eu, Mooney, M. Eu, Olsen, J. Eu, Piroué, P. Eu, Quan, X. Eu, Saka, H. Eu, Stickland, D. Eu, Tully, C. Eu, Werner, J. S. Eu, Zuranski, A. Eu, Brownson, E. Ev, Mendez, H. Ev, Ramirez Vargas, J. E. Ev, Barnes, V. E. Ew, Benedetti, D. Ew, Bolla, G. Ew, Bortoletto, D. Ew, De Mattia, M. Ew, Hu, Z. Ew, Jha, M. K. Ew, Jones, M. Ew, Jung, K. Ew, Kress, M. Ew, Leonardo, N. Ew, Lopes Pegna, D. Ew, Maroussov, V. Ew, Merkel, P. Ew, Miller, D. H. Ew, Neumeister, N. Ew, Radburn Smith, B. C. Ew, Shi, X. Ew, Shipsey, I. Ew, Silvers, D. Ew, Svyatkovskiy, A. Ew, Wang, F. Ew, Xie, W. Ew, Xu, L. Ew, Yoo, H. D. Ew, Zablocki, J. Ew, Zheng, Y. Ew, Parashar, N. Ex, Stupak, J. Ex, Adair, A. Ey, Akgun, B. Ey, Ecklund, K. M. Ey, Geurts, F. J. M. Ey, Li, W. Ey, Michlin, B. Ey, Padley, B. P. Ey, Redjimi, R. Ey, Roberts, J. Ey, Zabel, J. Ey, Betchart, B. Ez, Bodek, A. Ez, Covarelli, R. Ez, de Barbaro, P. Ez, Demina, R. Ez, Eshaq, Y. Ez, Ferbel, T. Ez, Garcia Bellido, A. Ez, Goldenzweig, P. Ez, Han, J. Ez, Harel, A. Ez, Khukhunaishvili, A. Ez, Petrillo, G. Ez, Vishnevskiy, D. Ez, Ciesielski, R. Fa, Demortier, L. Fa, Goulianos, K. Fa, Lungu, G. Fa, Mesropian, C. Fa, Arora, S. Fb, Barker, A. Fb, Chou, J. P. Fb, Contreras Campana, C. Fb, Contreras Campana, E. Fb, Duggan, D. Fb, Ferencek, D. Fb, Gershtein, Y. Fb, Gray, R. Fb, Halkiadakis, E. Fb, Hidas, D. Fb, Kaplan, S. Fb, Lath, A. Fb, Panwalkar, S. Fb, Park, M. Fb, Patel, R. Fb, Salur, S. Fb, Schnetzer, S. Fb, Somalwar, S. Fb, Stone, R. Fb, Thomas, S. Fb, Thomassen, P. Fb, Walker, M. Fb, Rose, K. Fc, Spanier, S. Fc, York, A. Fc, Bouhali, O. Fd, Hernandez, A. C. Fd, Eusebi, R. Fd, Flanagan, W. Fd, Gilmore, J. Fd, Kamon, T. Fd, Khotilovich, V. Fd, Krutelyov, V. Fd, Montalvo, R. Fd, Osipenkov, I. Fd, Pakhotin, Y. Fd, Perloff, A. Fd, Roe, J. Fd, Rose, A. Fd, Safonov, A. Fd, Sakuma, T. Fd, Suarez, I. Fd, Tatarinov, A. Fd, Akchurin, N. Fe, Cowden, C. Fe, Damgov, J. Fe, Dragoiu, C. Fe, Dudero, P. R. Fe, Faulkner, J. Fe, Kovitanggoon, K. Fe, Kunori, S. Fe, Lee, S. W. Fe, Libeiro, T. Fe, Volobouev, I. Fe, Appelt, E. Ff, Delannoy, A. G. Ff, Greene, S. Ff, Gurrola, A. Ff, Johns, W. Ff, Maguire, C. Ff, Mao, Y. Ff, Melo, A. Ff, Sharma, M. Ff, Sheldon, P. Ff, Snook, B. Ff, Tuo, S. Ff, Velkovska, J. Ff, Arenton, M. W. Fg, Boutle, S. Fg, Cox, B. Fg, Francis, B. Fg, Goodell, J. Fg, Hirosky, R. Fg, Ledovskoy, A. Fg, Li, H. Fg, Lin, C. Fg, Neu, C. Fg, Wood, J. Fg, Clarke, C. Fg, Harr, R. Fh, Karchin, P. E. Fh, Kottachchi Kankanamge Don, C. Fh, Lamichhane, P. Fh, Sturdy, J. Fh, Belknap, D. A. Fi, Carlsmith, D. Fi, Cepeda, M. Fi, Dasu, S. Fi, Dodd, L. Fi, Duric, S. Fi, Friis, E. Fi, Hall Wilton, R. Fi, Herndon, M. Fi, Hervé, A. Fi, Klabbers, P. Fi, Lanaro, A. Fi, Lazaridis, C. Fi, Levine, A. Fi, Loveless, R. Fi, Mohapatra, A. Fi, Ojalvo, I. Fi, Perry, T. Fi, Pierro, G. A. Fi, Polese, G. Fi, Ross, I. Fi, Sarangi, T. Fi, Savin, A. Fi, Smith, W. H. Fi, Vuosalo, C. Fi, and Woods, N. Fi
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Compact Muon Solenoid ,heavy ion: scattering ,ComputerSystemsOrganization_COMPUTERSYSTEMIMPLEMENTATION ,anisotropy [angular distribution] ,2760: 5020 GeV-cms/nucleon ,Large Hadron Collider (LHC) ,COLLABORATION ,transverse momentum dependence ,hadroproduction [K0(S)] ,High Energy Physics - Experiment ,High Energy Physics - Experiment (hep-ex) ,DEPENDENCE ,ComputingMilieux_COMPUTERSANDEDUCATION ,[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex] ,angular distribution: anisotropy ,NUCLEAR COLLISIONS ,Nuclear Experiment (nucl-ex) ,Nuclear Experiment ,angular correlation: two-particle ,Flow ,CMS ,Physics ,elliptic flow ,Ridge ,Long-range ,Correlations ,High-multiplicity ,ANGULAR-CORRELATIONS ,ROOT-S(NN)=5.02 TEV ,FLOW ,MULTIPLICITY ,SIDE ,lcsh:QC1-999 ,Correlation ,CERN LHC Coll ,ComputingMethodologies_DOCUMENTANDTEXTPROCESSING ,5020 GeV-cms/nucleon [2760] ,correlation [rapidity] ,rapidity: correlation ,transverse energy ,Nuclear and High Energy Physics ,QC1-999 ,kinetic ,FOS: Physical sciences ,[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex] ,charged particle: multiplicity ,multiplicity [charged particle] ,scattering [heavy ion] ,Nuclear Physics - Experiment ,ddc:530 ,heavy-ion collisions ,proton-ion collisions ,long-range correlations ,high-multiplicity ,p nucleus: scattering ,K0(S): hadroproduction ,Fisica delle particelle ,two-particle [angular correlation] ,lead ,Lambda: hadroproduction ,hadroproduction [Lambda] ,ComputingMilieux_THECOMPUTINGPROFESSION ,PARTICLE PHYSICS ,LARGE HADRON COLLIDER ,long-range [correlation] ,correlation: long-range ,Física ,scattering [p nucleus] ,High Energy Physics::Experiment ,lcsh:Physics ,experimental results - Abstract
Measurements of two-particle angular correlations between an identified strange hadron (K0S or Lambda/anti-Lambda) and a charged particle, emitted in pPb collisions, are presented over a wide range in pseudorapidity and full azimuth. The data, corresponding to an integrated luminosity of approximately 35 inverse nanobarns, were collected at a nucleon-nucleon center-of-mass energy (sqrt(s[NN])) of 5.02 TeV with the CMS detector at the LHC. The results are compared to semi-peripheral PbPb collision data at sqrt(s[NN]) = 2.76 TeV, covering similar charged-particle multiplicities in the events. The observed azimuthal correlations at large relative pseudorapidity are used to extract the second-order (v[2]) and third-order (v[3]) anisotropy harmonics of K0S and Lambda/anti-Lambda particles. These quantities are studied as a function of the charged-particle multiplicity in the event and the transverse momentum of the particles. For high-multiplicity pPb events, a clear particle species dependence of v[2] and v[3] is observed. For pt < 2 GeV, the v[2] and v[3] values of K0S particles are larger than those of Lambda/anti-Lambda particles at the same pt. This splitting effect between two particle species is found to be stronger in pPb than in PbPb collisions in the same multiplicity range. When divided by the number of constituent quarks and compared at the same transverse kinetic energy per quark, both v[2] and v[3] for K0S particles are observed to be consistent with those for Lambda/anti-Lambda particles at the 10% level in pPb collisions. This consistency extends over a wide range of particle transverse kinetic energy and event multiplicities., Replaced with published version. Added journal reference and DOI
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- 2014
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5. Histopathological and parasitological study of the gastrointestinal tract of dogs naturally infected with Leishmania infantum
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Pinto Aldair JW, Figueiredo Maria M, Silva Fabiana L, Martins Trycia, Michalick Marilene SM, Tafuri Washington L, and Tafuri Wagner L
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Veterinary medicine ,SF600-1100 - Abstract
Abstract Background The aim of this study was to provide a systematic pathological and parasitological overview of the gastrointestinal tract (GIT), including the stomach, duodenum, jejunum, ileum, caecum and colon, of dogs naturally infected with Leishmania. Methods Twenty mongrel dogs naturally infected with Leishmania (Leishmania) infantum and obtained from the Control Zoonosis Center of the Municipality of Ribeirão das Neves, Belo Horizonte Metropolitan area, Minas Gerais (MG) state, Brazil, were analyzed. The dogs were divided into two groups: Group 1 comprised nine clinically normal dogs and group 2 comprised 11 clinically affected dogs. After necropsy, one sample was collected from each GIT segment, namely the stomach, duodenum, jejunum, ileum, caecum and colon. Furthermore, paraffin-embedded samples were used for histological and parasitological (immunohistochemistry) evaluation and a morphometrical study were carried out to determine the parasite load (immunolabeled amastigote forms of Leishmania). The Friedman and the Mann Whitney tests were used for statistical analysis. The Friedman test was used to analyze each segment of the GIT within each group of dogs and the Mann Whitney test was used to compare the GIT segments between clinically unaffected and affected dogs. Results The infected dogs had an increased number of macrophages, plasma cells and lymphocytes, but lesions were generally mild. Parasite distribution in the GIT was evident in all intestinal segments and layers of the intestinal wall (mucosal, muscular and submucosal) irrespective of the clinical status of the dogs. However, the parasite load was statistically higher in the caecum and colon than in other segments of the GIT. Conclusion The high parasite burden evident throughout the GIT mucosa with only mild pathological alterations led us to consider whether Leishmania gains an advantage from the intestinal immunoregulatory response (immunological tolerance).
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- 2011
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6. A critical evaluation of the status of HPV vaccination in São Paulo State, Brazil.
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Martins TR, Witkin SS, Ferreira ADS, Viscondi JYK, Branquinho MSF, Cury L, Boas LSV, Longatto-Filho A, and Mendes-Corrêa MC
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- Humans, Brazil epidemiology, Female, Retrospective Studies, Adult, Papanicolaou Test statistics & numerical data, Young Adult, Middle Aged, Adolescent, Vaginal Smears statistics & numerical data, Vaccination statistics & numerical data, Uterine Cervical Neoplasms prevention & control, Uterine Cervical Neoplasms virology, Papillomavirus Vaccines administration & dosage, Papillomavirus Infections prevention & control
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Cervical cancer, whose well-recognized etiological agent is the Human Papillomavirus (HPV), is responsible for approximately 300,000 deaths worldwide, 80% of cases occurring in developing countries. In Brazil, 17,010 cases were expected, with 2,550 cases in São Paulo State, in 2023. The Papanicolaou test is the diagnostic method for the detection of precancerous lesions of the cervix, and HPV vaccination is now available for prevention., Materials and Methods: This is a descriptive and exploratory, retrospective investigation, carried out through analysis of data obtained from Brazilian Information Technology (DATASUS) of the Brazilian Federal Government: Cancer Information System (SISCAN), Brazilian National Immunization Program (PNI) and Mortality Information System (SIM). Electronic Library and data made available by the Government of the State of São Paulo., Results: The number of women in São Paulo State who underwent cytological examinations and histological tests for cervical cancer decreased between the Years 2013 and 2022., Conclusion: The continuous increase in cervical cancer over the study period was probably due to the lack of adherence to the primary and secondary prevention opportunities offered by the Public Health Authorities., Competing Interests: Declaration of competing interest The authors declare no conflicts of interest., (Copyright © 2024 HCFMUSP. Published by Elsevier España, S.L.U. All rights reserved.)
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- 2024
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7. Nanotopography and oral bacterial adhesion on titanium surfaces: in vitro and in vivo studies.
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Schwartz-Filho HO, Martins TR, Sano PR, Araújo MT, Chan DCH, Saldanha NR, Silva KP, Graziano TS, Brandt WC, Torres CVR, and Cogo-Müller K
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- Humans, Fusobacterium nucleatum, Microscopy, Electron, Scanning, Research Design, Bacterial Adhesion, Titanium
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The present study aimed to evaluate the influence of titanium surface nanotopography on the initial bacterial adhesion process by in vivo and in vitro study models. Titanium disks were produced and characterized according to their surface topography: machined (Ti-M), microtopography (Ti-Micro), and nanotopography (Ti-Nano). For the in vivo study, 18 subjects wore oral acrylic splints containing 2 disks from each group for 24 h (n = 36). After this period, the disks were removed from the splints and evaluated by microbial culture method, scanning electron microscopy (SEM), and qPCR for quantification of Streptococcus oralis, Actinomyces naeslundii, Fusobacterium nucleatum, as well as total bacteria. For the in vitro study, adhesion tests were performed with the species S. oralis and A. naeslundii for 24 h. Data were compared by ANOVA, with Tukey's post-test. Regarding the in vivo study, both the total aerobic and total anaerobic bacteria counts were similar among groups (p > 0.05). In qPCR, there was no difference among groups of bacteria adhered to the disks (p > 0.05), except for A. naeslundii, which was found in lower proportions in the Ti-Nano group (p < 0.05). In the SEM analysis, the groups had a similar bacterial distribution, with a predominance of cocci and few bacilli. In the in vitro study, there was no difference in the adhesion profile for S. oralis and A. naeslundii after 24 h of biofilm formation (p > 0.05). Thus, we conclude that micro- and nanotopography do not affect bacterial adhesion, considering an initial period of biofilm formation.
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- 2024
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8. Intranasal Liposomal Formulation of Spike Protein Adjuvanted with CpG Protects and Boosts Heterologous Immunity of hACE2 Transgenic Mice to SARS-CoV-2 Infection.
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Russo M, Mendes-Corrêa MC, Lins BB, Kersten V, Pernambuco Filho PCA, Martins TR, Tozetto-Mendoza TR, Vilas Boas LS, Gomes BM, Dati LMM, Duarte-Neto AN, Reigado GR, Frederico ABT, de Brito E Cunha DRA, de Paula AV, da Silva JIG, Vasconcelos CFM, Chambergo FS, Nunes VA, Ano Bom APD, Castilho LR, Martins RAP, Hirata MH, and Mirotti L
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Mucosal vaccination appears to be suitable to protect against SARS-CoV-2 infection. In this study, we tested an intranasal mucosal vaccine candidate for COVID-19 that consisted of a cationic liposome containing a trimeric SARS-CoV-2 spike protein and CpG-ODNs, a Toll-like receptor 9 agonist, as an adjuvant. In vitro and in vivo experiments indicated the absence of toxicity following the intranasal administration of this vaccine formulation. First, we found that subcutaneous or intranasal vaccination protected hACE-2 transgenic mice from infection with the wild-type (Wuhan) SARS-CoV-2 strain, as shown by weight loss and mortality indicators. However, when compared with subcutaneous administration, the intranasal route was more effective in the pulmonary clearance of the virus and induced higher neutralizing antibodies and anti-S IgA titers. In addition, the intranasal vaccination afforded protection against gamma, delta, and omicron virus variants of concern. Furthermore, the intranasal vaccine formulation was superior to intramuscular vaccination with a recombinant, replication-deficient chimpanzee adenovirus vector encoding the SARS-CoV-2 spike glycoprotein (Oxford/AstraZeneca) in terms of virus lung clearance and production of neutralizing antibodies in serum and bronchial alveolar lavage (BAL). Finally, the intranasal liposomal formulation boosted heterologous immunity induced by previous intramuscular vaccination with the Oxford/AstraZeneca vaccine, which was more robust than homologous immunity.
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- 2023
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9. Impact of the COVID-19 Pandemic on Cervical Cancer Screening in São Paulo State, Brazil.
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Martins TR, Witkin SS, Mendes-Corrêa MC, Godoy AS, Cury L, Balancin ML, Ab'Saber AM, Peres SV, Messias S, Tozetto Mendoza TR, and Longatto-Filho A
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- Female, Humans, Brazil epidemiology, Vaginal Smears, Early Detection of Cancer, Pandemics, SARS-CoV-2, Papanicolaou Test, Mass Screening, Uterine Cervical Neoplasms diagnosis, Uterine Cervical Neoplasms epidemiology, Uterine Cervical Neoplasms pathology, COVID-19 epidemiology, Uterine Cervical Dysplasia pathology
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Introduction: The early identification of precursor lesions followed by appropriate treatment prevents development of cervical cancer and its consequences., Objective: The present study evaluated the influence of the COVID-19 pandemic on cervical cancer screening by comparing the quantity of tests to detect cervical cellular changes performed in São Paulo state in 2019, prior to the detection of SARS-CoV-2 in Brazil, to the first (2020) and second (2021) years following its appearance., Materials and Methods: Data from Fundação Oncocentro de São Paulo (FOSP), the agency that analyses approximately 220,000 Papanicolaou (Pap) tests annually, were reviewed., Results: A median of 1,835 Pap tests were performed in 55 municipalities in 2019. This was reduced to 815 tests in 2020, a 56% decrease (p = 0.0026). In 2021, the median number was 1,745, a 53% increase over 2020 levels (p = 0.0233). The 26 municipalities with >1,000 tests in 2020 had a median reduction from 4,433 in 2019 to 2,580 in 2020 (p = 0. 0046). The 29 municipalities with <1,000 tests had a median reduction from 951 in 2019 to 554 in 2020 (p < 0.0001). There was a 44% reduction in the number of follow-up cytological evaluations from 2019 to 2020, followed by a 30% increase in the following year. However, the percentage of women with a normal finding or with any abnormality remained unchanged. The findings from a histological evaluation of women in São Paulo city indicated that the percent of cases positive for CIN-1 (p < 0.0410) and CIN-3 (p < 0.0012) increased in 2020 and 2021 as compared to 2019 levels., Conclusion: A reduction in testing for cervical cancer in the first year of the COVID-19 pandemic, accompanied by an elevated incidence of precancerous lesions in each of the first 2 years following its initiation, may portend a subsequent increased occurrence of cervical cancer in Brazil., (© 2023 S. Karger AG, Basel.)
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- 2023
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10. A Collaborative Classroom Investigation of the Evolution of SABATH Methyltransferase Substrate Preference Shifts over 120 My of Flowering Plant History.
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Dubs NM, Davis BR, de Brito V, Colebrook KC, Tiefel IJ, Nakayama MB, Huang R, Ledvina AE, Hack SJ, Inkelaar B, Martins TR, Aartila SM, Albritton KS, Almuhanna S, Arnoldi RJ, Austin CK, Battle AC, Begeman GR, Bickings CM, Bradfield JT, Branch EC, Conti EP, Cooley B, Dotson NM, Evans CJ, Fries AS, Gilbert IG, Hillier WD, Huang P, Hyde KW, Jevtovic F, Johnson MC, Keeler JL, Lam A, Leach KM, Livsey JD, Lo JT, Loney KR, Martin NW, Mazahem AS, Mokris AN, Nichols DM, Ojha R, Okorafor NN, Paris JR, Reboucas TF, Sant'Anna PB, Seitz MR, Seymour NR, Slaski LK, Stemaly SO, Ulrich BR, Van Meter EN, Young ML, and Barkman TJ
- Subjects
- Methylation, Phylogeny, Salicylic Acid metabolism, Substrate Specificity, Magnoliopsida classification, Magnoliopsida enzymology, Methyltransferases genetics, Methyltransferases metabolism, Plant Proteins genetics, Plant Proteins metabolism
- Abstract
Next-generation sequencing has resulted in an explosion of available data, much of which remains unstudied in terms of biochemical function; yet, experimental characterization of these sequences has the potential to provide unprecedented insight into the evolution of enzyme activity. One way to make inroads into the experimental study of the voluminous data available is to engage students by integrating teaching and research in a college classroom such that eventually hundreds or thousands of enzymes may be characterized. In this study, we capitalize on this potential to focus on SABATH methyltransferase enzymes that have been shown to methylate the important plant hormone, salicylic acid (SA), to form methyl salicylate. We analyze data from 76 enzymes of flowering plant species in 23 orders and 41 families to investigate how widely conserved substrate preference is for SA methyltransferase orthologs. We find a high degree of conservation of substrate preference for SA over the structurally similar metabolite, benzoic acid, with recent switches that appear to be associated with gene duplication and at least three cases of functional compensation by paralogous enzymes. The presence of Met in active site position 150 is a useful predictor of SA methylation preference in SABATH methyltransferases but enzymes with other residues in the homologous position show the same substrate preference. Although our dense and systematic sampling of SABATH enzymes across angiosperms has revealed novel insights, this is merely the "tip of the iceberg" since thousands of sequences remain uncharacterized in this enzyme family alone., (© The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.)
- Published
- 2022
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11. Moving towards a strategy to accelerate cervical cancer elimination in a high-burden city-Lessons learned from the Amazon city of Manaus, Brazil.
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Torres KL, Rondon HHMF, Martins TR, Martins S, Ribeiro A, Raiol T, Marques CP, Corrêa F, Migowski A, Minuzzi-Souza TTCE, Schiffman M, Rodriguez AC, and Gage JC
- Abstract
The World Health Organization Call to Eliminate Cervical Cancer resonates in cities like Manaus, Brazil, where the burden is among the world's highest. Manaus has offered free cytology-based screening since 1990 and HPV immunization since 2013, but the public system is constrained by many challenges and performance is not well-defined. We obtained cervical cancer prevention activities within Manaus public health records for 2019 to evaluate immunization and screening coverage, screening by region and neighborhood, and the annual Pink October screening campaign. We estimated that among girls and boys age 14-18, 85.9% and 64.9% had 1+ doses of HPV vaccine, higher than rates for age 9-13 (73.4% and 43.3%, respectively). Of the 90,209 cytology tests performed, 24.9% were outside the target age and the remaining 72,230 corresponded to 40.1% of the target population (one-third of women age 25-64). The East zone had highest screening coverage (49.1%), highest high-grade cytology rate (2.5%) and lowest estimated cancers (38.1/100,000) compared with the South zone (32.9%, 1.8% and 48.5/100,000, respectively). Largest neighborhoods had fewer per capita screening locations, resulting in lower coverage. During October, some clinics successfully achieved higher screening volumes and high-grade cytology rates (up to 15.4%). Although we found evidence of some follow-up within 10 months post-screening for 51/70 women (72.9%) with high-grade or worse cytology, only 18 had complete work-up confirmed. Manaus has successfully initiated HPV vaccination, forecasting substantial cervical cancer reductions by 2050. With concerted efforts during campaigns, some clinics improved screening coverage and reached high-risk women. Screening campaigns in community locations in high-risk neighborhoods using self-collected HPV testing can achieve widespread coverage. Simplifying triage and treatment with fewer visits closer to communities would greatly improve follow-up and program effectiveness. Achieving WHO Cervical Cancer Elimination goals in high-burden cities will require major reforms for screening and simpler follow-up and treatment., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2021
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12. Recovery of copper and aluminium from coaxial cable wastes using comparative mechanical processes analysis.
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Martins TR, Mrozinski NS, Bertuol DA, and Tanabe EH
- Subjects
- Mechanical Phenomena, Metals, Recycling, Aluminum, Copper
- Abstract
This work aims to perform a comparative study of two mechanical processes for the recycling of metals from coaxial cables (aluminium and copper-clad steel): Process I - comminution, sieving and electrostatic separation; and Process II - comminution, magnetic separation and electrostatic separation. Characterization techniques were performed on the cables to discover their composition. The parameters evaluated of electrostatic separation were: roll speed ( n ), electrostatic electrode distance (D2), voltage applied to the electrodes ( U ) and splitter angle ( γ ). The best conditions for electrostatic separation were: Process I - n = 30 rpm, D2 = 8 cm, U = 30 kV and γ = 0°; Process II - n = 10 rpm, D2 = 10 cm, U = 25 kV and γ = 2.5°. Process I presented aluminium with purity of 99.51% and recovery efficiency of 94.53%, as well as copper-clad steel with purity of 96.79% and recovery efficiency of 99.68%. Process II presented aluminium with purity of 96.51% and recovery of 70.12%, as well as copper-clad steel with purity of 99.53% and recovery of 99.46%. A simplified economic assessment was performed on both process, and Process I has demonstrated to be the most profitable for coaxial cable recycling. The results showed that Process I is promising for the recovery of metals from cables due to its simplicity and lower cost, being capable of wide application to other processes that contain a mixture of conductive and non-conductive particles.
- Published
- 2021
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13. Attendance for diagnostic colposcopy among high-risk human papillomavirus positive women in a Brazilian feasibility study.
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Buss LF, Levi JE, Longatto-Filho A, Cohen DD, Cury L, Martins TR, Fuza LM, Villa LL, and Eluf-Neto J
- Subjects
- Adult, Brazil, Cohort Studies, Feasibility Studies, Female, Humans, Middle Aged, Prospective Studies, Colposcopy, Papillomaviridae isolation & purification, Papillomavirus Infections pathology, Patient Compliance, Uterine Cervical Neoplasms pathology, Uterine Cervical Dysplasia pathology
- Abstract
Objective: To investigate factors associated with colposcopy attendance in HPV-positive women in São Paulo, Brazil., Methods: We analyzed data from a prospective cohort of women positive for high-risk HPV (hr-HPV) undergoing cervical cancer screening in primary care services in São Paulo, Brazil. Non-pregnant women attending routine screening between December 2014 and March 2016 were offered an hr-HPV test, and those testing positive and aged 25 years or older were invited for colposcopy. Sociodemographic information was recorded at study enrollment. We compared variables between women who did and did not attend colposcopy within a logistic regression framework., Results: Of 1537 hr-HPV-positive women, 1235 (80.4%) attended for colposcopy, with a median time from primary test to colposcopy of 132 days. Younger age (P<0.001) and concurrent negative cytology results (P=0.025) were associated with lower attendance. Women registered at units providing both the primary test and colposcopy were more likely to attend than those at units making external referrals (788/862 [91.4%] versus 447/675 [66.2%], P<0.001)., Conclusion: Non-attendance for colposcopy may limit the success of future screening programs based on hr-HPV testing in Brazil. Transfer of colposcopy services to primary care is a simple and effective facilitator of attendance., (© 2020 International Federation of Gynecology and Obstetrics.)
- Published
- 2021
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14. Lymphocyte activation after a high-intensity street dance class.
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Borges L, Gorjão R, Gray SR, Martins TR, Santos VC, Momesso CM, Pithon-Curi TC, and Hatanaka E
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- Creatine Kinase, MB Form blood, Dancing education, Heart Rate, Humans, Inflammation, Lymphocyte Count, Male, Reactive Oxygen Species blood, Tetradecanoylphorbol Acetate pharmacology, Young Adult, Dancing physiology, L-Selectin analysis, Lymphocyte Activation drug effects
- Abstract
Intense dance training leads to inflammation, which may impair the health and performance of the practitioners. Herein, we evaluate the effect of a single street dancing class on the profile of muscle enzymes, lymphocyte activation, and cell surface CD62L expression. We also investigated the correlation between muscle enzymes, adhesion molecules, and lymphocyte activation in dancers. Fifteen male participants (mean ± standard error: age 22.4 ± 1.08 years, body mass index 24.8 ± 0.69 kg/m2, body fat 12.3 ± 1.52%), who were amateur dancers, had blood samples collected previously and subsequent to a high-intensity street dance class. After the class, dancers showed an increase in total lymphocyte count (2.0-fold), creatine kinase (CK)-NAC (4.87%), and CK-MB (3.36%). We also observed a decrease (2.5-fold) in reactive oxygen species (ROS) produced by lymphocytes, under phorbol myristate acetate-stimulated environments. Following the dance class, CD62L expression in lymphocytes decreased (51.42%), while there was a negative correlation between the intensity of the exercise and CD62L expression (r = -0.73; p = 0.01). Lymphocytes were less responsive to stimuli after a single bout of street dancing, indicating transient immunosuppression., Competing Interests: The authors have declared that no competing interests exist.
- Published
- 2020
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15. Flexible 3D Cell-Based Platforms for the Discovery and Profiling of Novel Drugs Targeting Plasmodium Hepatic Infection.
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Arez F, Rebelo SP, Fontinha D, Simão D, Martins TR, Machado M, Fischli C, Oeuvray C, Badolo L, Carrondo MJT, Rottmann M, Spangenberg T, Brito C, Greco B, Prudêncio M, and Alves PM
- Subjects
- Animals, Antimalarials chemistry, Female, Humans, Liver parasitology, Liver Diseases, Parasitic parasitology, Malaria parasitology, Male, Mice, Mice, Inbred BALB C, Plasmodium berghei physiology, Plasmodium falciparum drug effects, Plasmodium falciparum physiology, Antimalarials administration & dosage, Drug Discovery methods, Liver Diseases, Parasitic drug therapy, Malaria drug therapy, Plasmodium berghei drug effects
- Abstract
The restricted pipeline of drugs targeting the liver stage of Plasmodium infection reflects the scarcity of cell models that mimic the human hepatic phenotype and drug metabolism, as well as Plasmodium hepatic infection. Using stirred-tank culture systems, spheroids of human hepatic cell lines were generated, sustaining a stable hepatic phenotype over 4 weeks of culture. Spheroids were employed in the establishment of 3D Plasmodium berghei infection platforms that relied on static or dynamic culture conditions. P. berghei invasion and development were recapitulated in the hepatic spheroids, yielding blood-infective merozoites. The translational potential of the 3D platforms was demonstrated by comparing the in vitro minimum inhibitory concentration of M5717, a compound under clinical development, with in vivo plasma concentrations that clear liver stage P. berghei in mice. Our results show that the 3D platforms are flexible and scalable and can predict the efficacy of antiplasmodial therapies, constituting a powerful tool for integration in drug discovery programs.
- Published
- 2019
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16. High-Risk HPV Testing in Primary Screening for Cervical Cancer in the Public Health System, São Paulo, Brazil.
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Levi JE, Martins TR, Longatto-Filho A, Cohen DD, Cury L, Fuza LM, Villa LL, and Eluf-Neto J
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Brazil, Cervix Uteri diagnostic imaging, Cervix Uteri pathology, Cervix Uteri virology, Child, Colposcopy statistics & numerical data, DNA, Viral isolation & purification, Early Detection of Cancer methods, Early Detection of Cancer statistics & numerical data, Female, Humans, Mass Screening methods, Mass Screening statistics & numerical data, Middle Aged, Papillomaviridae genetics, Papillomaviridae isolation & purification, Papillomavirus Infections pathology, Papillomavirus Infections virology, Uterine Cervical Neoplasms pathology, Uterine Cervical Neoplasms virology, Vaginal Smears statistics & numerical data, Young Adult, Uterine Cervical Dysplasia pathology, Uterine Cervical Dysplasia virology, Human Papillomavirus DNA Tests statistics & numerical data, National Health Programs statistics & numerical data, Papillomavirus Infections diagnosis, Uterine Cervical Neoplasms prevention & control, Uterine Cervical Dysplasia diagnosis
- Abstract
Every year there are approximately 16,000 new cases of cervical cancer in Brazil. Novel screening technologies may reduce this number by expanding the population coverage but also by improving the detection rate of precursor lesions. We aimed to evaluate human papillomaviruses (HPV)-DNA testing in the context of routine cervical cancer screening in the public health system of the city of São Paulo, Brazil. Women participating in the primary screening program were invited to enroll. Liquid-based cytology samples were collected and cytology and Hr-HPV DNA testing were performed in parallel. Cytologists were blind to HPV results. Women older than 24 years with a positive high-risk HPV test and/or cytology class ≥ ASC-US were referred to colposcopy. From December 2014 to December 2016, 16,102 women joined the study. High-risk human papillomavirus (HR HPV) DNA prevalence was 14.9%, whereas cytologic abnormalities were found in 7.2% of the women. Per protocol, 1,592 Hr-HPV
+ women, in addition to 72 patients with cytologic classification > low-grade squamous intraepithelial lesion (LSIL) were referred. A total of 80 cervical intraepithelial neoplasia (CIN2+ ) cases were diagnosed, 79 were Hr-HPV DNA+ and 18 had normal cytology. Hr-HPV DNA detected a significant number of patients with premalignant lesions missed by cytology and all 16 CIN3+ cases were Hr-HPV DNA+ HPV genotyping may be useful in the management of Hr-HPV+ women, reducing the burden of colposcopic referral for those harboring genotypes with a weaker association to CIN3+ Use of HPV-DNA testing was shown to be feasible and advantageous over current cytologic screening in the public health system., (©2019 American Association for Cancer Research.)- Published
- 2019
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17. Self-sampling coupled to the detection of HPV 16 and 18 E6 protein: A promising option for detection of cervical malignancies in remote areas.
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Torres KL, Mariño JM, Pires Rocha DA, de Mello MB, de Melo Farah HH, Reis RDS, Alves VDCR, Gomes E, Martins TR, Soares AC, de Oliveira CM, and Levi JE
- Subjects
- Adolescent, Adult, Brazil epidemiology, Colposcopy, DNA, Viral analysis, Early Detection of Cancer methods, Female, Humans, Middle Aged, Papillomavirus Infections diagnosis, Papillomavirus Infections epidemiology, Rural Population, Specimen Handling, Uterine Cervical Neoplasms diagnosis, Uterine Cervical Neoplasms epidemiology, Vaginal Smears methods, Young Adult, DNA-Binding Proteins analysis, Human papillomavirus 16 isolation & purification, Human papillomavirus 18 isolation & purification, Oncogene Proteins, Viral analysis, Papillomavirus Infections virology, Repressor Proteins analysis, Uterine Cervical Neoplasms virology
- Abstract
Objective: To evaluate both the performance and acceptability of a method coupling self-sampling with detection of cervical malignancy via elevated HPV 16 and 18 E6 oncoproteins (OncoE6™ Cervical Test) in remote areas in Brazil., Methods: Women living in rural villages in proximity to Coari city, Amazonas, Brazil were invited to participate in a cervical cancer screening study. 412 subjects were enrolled; there were no refusals. In addition to E6 protein detection, DNA was extracted from the brushes and evaluated for HPV genotypes by PCR (PGMY09/11), followed by typing by the Papillocheck™ if positive. Subjects who were found to be positive for OncoE6 or HPV-DNA were referred for colposcopy., Results: For 110 subjects (27%) this was the first cervical cancer exam. Overall the HPV-DNA prevalence was 19.1% (n = 79); 1.4% (n = 6) were positive by the OncoE6 Test. Fifty-six women attended the invitation for colposcopy where nine had an abnormal cervix and were subsequently biopsied. Histopathological analysis revealed 2 CIN3, 2 carcinomas and 5 CIN1. OncoE6 called two out of the three HPV 16 or 18 associated CIN3+ lesions., Conclusions: The findings suggest that self-administered sample collection in combination with OncoE6 Test is feasible in this population. This could enable expanded screening coverage while ensuring a high specificity which is imperative given the remote geographic location, since women bearing abnormal test results would necessitate travel and logistical burden to access colposcopy and treatment., Competing Interests: JE Levi has received travel support from Arbor Vita Corporation, research support in the form of equipment and reagents from BD and speakers fee from Roche Diagnostics in the last 5 years. Other authors do not have any potential conflict of interest to disclose.
- Published
- 2018
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18. 3D-3-culture: A tool to unveil macrophage plasticity in the tumour microenvironment.
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Rebelo SP, Pinto C, Martins TR, Harrer N, Estrada MF, Loza-Alvarez P, Cabeçadas J, Alves PM, Gualda EJ, Sommergruber W, and Brito C
- Subjects
- Antineoplastic Agents pharmacology, Apoptosis, Carcinoma, Non-Small-Cell Lung, Cell Communication, Cell Line, Tumor, Cell Movement, Cell Plasticity, Cell Proliferation, Cell Survival, Extracellular Matrix metabolism, Fibroblasts cytology, Fibroblasts drug effects, Fibroblasts physiology, Humans, Macrophages cytology, Macrophages drug effects, Monocytes cytology, Monocytes drug effects, Monocytes physiology, Myeloid Cells, Neoplasm Invasiveness, Spheroids, Cellular cytology, Spheroids, Cellular physiology, Tumor Microenvironment drug effects, Cell Culture Techniques, Macrophages physiology, Tumor Microenvironment physiology
- Abstract
The tumour microenvironment (TME) shapes disease progression and influences therapeutic response. Most aggressive solid tumours have high levels of myeloid cell infiltration, namely tumour associated macrophages (TAM). Recapitulation of the interaction between the different cellular players of the TME, along with the extracellular matrix (ECM), is critical for understanding the mechanisms underlying disease progression. This particularly holds true for prediction of therapeutic response(s) to standard therapies and interrogation of efficacy of TME-targeting agents. In this work, we explored a culture platform based on alginate microencapsulation and stirred culture systems to develop the 3D-3-culture, which entails the co-culture of tumour cell spheroids of non-small cell lung carcinoma (NSCLC), cancer associated fibroblasts (CAF) and monocytes. We demonstrate that the 3D-3-culture recreates an invasive and immunosuppressive TME, with accumulation of cytokines/chemokines (IL4, IL10, IL13, CCL22, CCL24, CXCL1), ECM elements (collagen type I, IV and fibronectin) and matrix metalloproteinases (MMP1/9), supporting cell migration and promoting cell-cell interactions within the alginate microcapsules. Importantly, we show that both the monocytic cell line THP-1 and peripheral blood-derived monocytes infiltrate the tumour tissue and transpolarize into an M2-like macrophage phenotype expressing CD68, CD163 and CD206, resembling the TAM phenotype in NSCLC. The 3D-3-culture was challenged with chemo- and immunotherapeutic agents and the response to therapy was assessed in each cellular component. Specifically, the macrophage phenotype was modulated upon treatment with the CSF1R inhibitor BLZ945, resulting in a decrease of the M2-like macrophages. In conclusion, the crosstalk between the ECM and tumour, stromal and immune cells in microencapsulated 3D-3-culture promotes the activation of monocytes into TAM, mimicking aggressive tumour stages. The 3D-3-culture constitutes a novel tool to study tumour-immune interaction and macrophage plasticity in response to external stimuli, such as chemotherapeutic and immunomodulatory drugs., (Copyright © 2018 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2018
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19. PCR-RFLP assay as an option for primary HPV test.
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Golfetto L, Alves EV, Martins TR, Sincero TCM, Castro JBS, Dannebrock C, Oliveira JG, Levi JE, Onofre ASC, and Bazzo ML
- Subjects
- Adolescent, Adult, Aged, Early Detection of Cancer, Female, Genotype, Humans, Mass Screening, Microarray Analysis, Middle Aged, Papillomavirus Infections virology, Polymerase Chain Reaction, Polymorphism, Restriction Fragment Length, Sensitivity and Specificity, Uterine Cervical Neoplasms virology, Young Adult, Papillomaviridae genetics, Papillomavirus Infections diagnosis, Uterine Cervical Neoplasms diagnosis
- Abstract
Persistent human papillomavirus (HPV) infection is an essential factor of cervical cancer. This study evaluated the analytical performance of restriction fragment length polymorphism polymerase chain reaction (PCR-RFLP) assay compared to PapilloCheck® microarray to identify human papilloma virus (HPV) in cervical cells. Three hundred and twenty-five women were analyzed. One sample was used for conventional cytology and another sample was collected using BD SurePath™ kit for HPV tests. Eighty samples (24.6%) were positive for HPV gene by PCR-Multiplex and were then submitted to PCR-RFLP and PapilloCheck® microarray. There was a genotyping agreement in 71.25% (57/80) on at least one HPV type between PCR-RFLP and PapilloCheck® microarray. In 22 samples (27.5%), the results were discordant and those samples were additionally analyzed by DNA sequencing. HPV 16 was the most prevalent HPV type found in both methods, followed by HPVs 53, 68, 18, 39, and 66 using PCR-RFLP analysis, and HPVs 39, 53, 68, 56, 31, and 66 using PapilloCheck® microarray. In the present study, a perfect agreement using Cohen's kappa (κ) was found in HPV 33 and 58 (κ=1), very good for HPV 51, and good for types 16, 18, 53, 59, 66, 68, 70, and 73. PCR-RFLP analysis identified only 25% (20/80) HPV coinfection, and PapilloCheck® microarray found 62.5% (50/80). Our Cohen's kappa results indicate that our in-house HPV genotyping testing (PCR-RFLP analysis) could be applied as a primary HPV test screening, especially in low income countries. If multiple HPV types are found in this primary test, a more descriptive test, such as PapilloCheck® microarray, could be performed.
- Published
- 2018
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20. Influence of Prior Knowledge of Human Papillomavirus Status on the Performance of Cytology Screening.
- Author
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Martins TR, Longatto-Filho A, Cohen D, Viscondi JYK, Fuza LM, Cury L, Villa LL, Levi JE, and Eluf-Neto J
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Female, Humans, Middle Aged, Papillomavirus Infections diagnosis, Sensitivity and Specificity, Single-Blind Method, Uterine Cervical Neoplasms diagnosis, Uterine Cervical Neoplasms virology, Young Adult, Uterine Cervical Dysplasia diagnosis, Uterine Cervical Dysplasia virology, Clinical Competence, Papillomavirus Infections complications, Uterine Cervical Neoplasms pathology, Vaginal Smears, Uterine Cervical Dysplasia pathology
- Abstract
Objectives: This study aimed to evaluate the influence of prior knowledge of human papillomavirus (HPV) status in cervical cytopathology readings., Methods: Participants comprised 2,376 women who underwent parallel cytology and HPV-DNA testing. Smears were read twice by the same team, first with previous knowledge of HPV-DNA status., Results: Overall, 239 (10.2%) smears had their cytology classification altered by the HPV-informed review. Cytology readings with prior knowledge of the HPV status revealed 10.5% of abnormal smears (atypical squamous cells of undetermined significance or higher), while without prior knowledge, this rate dropped to 7.6%. When HPV status was informed, a significant increase in all categories of altered smears was observed. Cytology with prior knowledge of HPV status detected more cervical intraepithelial neoplasia grade 2 or higher (CIN 2+) compared with blinded: 86.7% vs 60.0%., Conclusions: Our data indicate that cytology interpreted with prior knowledge of the HPV status provides higher sensitivity for CIN 2+ lesions while marginally reducing the overall specificity compared with HPV status blinded cytology.
- Published
- 2018
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21. Berberine-induced cardioprotection and Sirt3 modulation in doxorubicin-treated H9c2 cardiomyoblasts.
- Author
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Coelho AR, Martins TR, Couto R, Deus C, Pereira CV, Simões RF, Rizvanov AA, Silva F, Cunha-Oliveira T, Oliveira PJ, and Serafim TL
- Subjects
- Cell Line, Doxorubicin pharmacology, Humans, Muscle Proteins metabolism, Myoblasts, Cardiac pathology, Berberine pharmacology, Cardiotonic Agents pharmacology, Doxorubicin adverse effects, Myoblasts, Cardiac enzymology, Oxidative Stress drug effects, Sirtuin 3 metabolism
- Abstract
Doxorubicin (DOX) is one of the most widely used anti-neoplastic agents. However, treatment with DOX is associated with cumulative cardiotoxicity inducing progressive cardiomyocyte death. Sirtuin 3 (Sirt3), a mitochondrial deacetylase, regulates the activity of proteins involved in apoptosis, autophagy and metabolism. Our hypothesis is that pharmacological modulation by berberine (BER) pre-conditioning of Sirt3 protein levels decreases DOX-induced cardiotoxicity. Our results showed that DOX induces cell death in all experimental groups. Increase in Sirt3 content by transfection-mediated overexpression decreased DOX cytotoxicity, mostly by maintaining mitochondrial network integrity and reducing oxidative stress. p53 was upregulated by DOX, and appeared to be a direct target of Sirt3, suggesting that Sirt3-mediated protection against cell death could be related to this protein. BER pre-treatment increased Sirt3 and Sirt1 protein levels in the presence of DOX and inhibited DOX-induced caspase 9 and 3-like activation. Moreover, BER modulated autophagy in DOX-treated H9c2 cardiomyoblasts. Interestingly, mitochondrial biogenesis markers were upregulated in in BER/DOX-treated cells. Sirt3 over-expression contributes to decrease DOX cytotoxicity on H9c2 cardiomyoblasts, while BER can be used as a modulator of Sirtuin function and cell quality control pathways to decrease DOX toxicity., (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Published
- 2017
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22. How petals change their spots: cis-regulatory re-wiring in Clarkia (Onagraceae).
- Author
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Martins TR, Jiang P, and Rausher MD
- Subjects
- Alleles, Biological Evolution, Chromosome Segregation genetics, Flowers genetics, Gene Expression Regulation, Plant, Luciferases metabolism, Phylogeny, Plant Proteins metabolism, Promoter Regions, Genetic, Species Specificity, Transcription Factors metabolism, Clarkia anatomy & histology, Clarkia genetics, Flowers anatomy & histology, Regulatory Sequences, Nucleic Acid genetics
- Abstract
A long-standing question in evolutionary developmental biology is how new traits evolve. Although most floral pigmentation studies have focused on how pigment intensity and composition diversify, few, if any, have explored how a pattern element can shift position. In the present study, we examine the genetic changes underlying shifts in the position of petal spots in Clarkia. Comparative transcriptome analyses were used to identify potential candidate genes responsible for spot formation. Co-segregation analyses in F
2 individuals segregating for different spot positions, quantitative PCR, and pyrosequencing, were used to confirm the role of the candidate gene in determining spot position. Transient expression assays were used to identify the expression domain of different alleles. An R2R3Myb transcription factor (CgMyb1) activated spot formation, and different alleles of CgMyb1 were expressed in different domains, leading to spot formation in different petal locations. Reporter assays revealed that promoters from different alleles determine different locations of expression. The evolutionary shift in spot position is due to one or more cis-regulatory changes in the promoter of CgMyb1, indicating that shifts in pattern element position can be caused by changes in a single gene, and that cis-regulatory rewiring can be used to alter the relative position of an existing character., (© 2016 The Authors. New Phytologist © 2016 New Phytologist Trust.)- Published
- 2017
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23. Multiple HPV genotype infection impact on invasive cervical cancer presentation and survival.
- Author
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Nogueira Dias Genta ML, Martins TR, Mendoza Lopez RV, Sadalla JC, de Carvalho JPM, Baracat EC, Levi JE, and Carvalho JP
- Subjects
- Alphapapillomavirus genetics, Female, Humans, Alphapapillomavirus classification, Genotype, Uterine Cervical Neoplasms virology
- Abstract
Background: Invasive cervical cancer (ICC) is the third most common malignant neoplasm affecting Brazilian women. Little is known about the impact of specific HPV genotypes in the prognosis of ICC. We hypothesized that HPV genotype would impact ICC clinical presentation and survival., Methods: Women diagnosed with ICC at the Instituto do Câncer do Estado de São Paulo (ICESP) between May 2008 and June 2012 were included in the study and were followed until December 2015. HPV genotype was detected from formalin-fixed paraffin-embedded (FFPE) tumor tissue samples using Onclarity™ system (BD Viper™ LT automated system)., Results: 292 patients aged 50±14 years were analyzed. HPVDNA was detected in 84% of patients. The HPV genotypes studied were: HPV16 (64%), HPV18 (10%), HPV33-58 (7%), HPV45 (5%), HPV31 (4%) and other high-risk HPV genotypes (11%). HPV genotypes showed different distributions regarding histological type and clinical stage. Patients were followed for 35±21 months. The overall survival at 5 years after diagnosis of cervical cancer was 54%. Age, clinical staging, histological type and multiple HPV genotypes infection detected in the same tumor specimen were associated with poorer overall survival on multivariate Cox proportional hazard analysis (p<0.05). No specific HPV genotype affected survival., Conclusion: Multiple HPV genotype infection was associated with poorer ICC survival in our study, compared with single genotype infection. HPV genotyping from FFPE tumor tissue using an automated assay such as the Onclarity BD™ assay provides a simpler alternative for routine clinical use., Impact: This is the largest study employing an automated HPV genotyping assay using FFPE of ICC. Multiple HPV genotype infection adversely influenced survival.
- Published
- 2017
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24. HPV genotype distribution in Brazilian women with and without cervical lesions: correlation to cytological data.
- Author
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Martins TR, Mendes de Oliveira C, Rosa LR, de Campos Centrone C, Rodrigues CL, Villa LL, and Levi JE
- Subjects
- Adolescent, Adult, Aged, Aged, 80 and over, Brazil epidemiology, Female, Genotype, Humans, Middle Aged, Papillomaviridae classification, Papillomaviridae genetics, Papillomavirus Infections diagnosis, Papillomavirus Infections epidemiology, Uterine Cervical Neoplasms diagnosis, Uterine Cervical Neoplasms epidemiology, Uterine Cervical Neoplasms virology, Vaginal Smears, Young Adult, Papillomaviridae isolation & purification, Papillomavirus Infections virology
- Abstract
Background: Human Papillomavirus (HPV) genotype distribution varies according to the method of assessment and population groups. This study analyzed type-specific HPV infections among women ranging from 14-95 years old, displaying normal and abnormal cytology, from São Paulo and Barretos cities, Brazil., Methods: Women found positive for High Risk-HPVs DNA by either the Hybrid Capture 2 (HC2) or Cobas HPV Test (n = 431) plus a random sample of 223 negative by both assays and 11 samples with indeterminate results, totalizing 665 samples, were submitted to HPV detection by the PapilloCheck test. Cytological distribution included 499 women with a cytological result of Negative for Intraepithelial Lesion or Malignancy and 166 with some abnormality as follows: 54 Atypical Squamous Cells of Undetermined Significance; 66 Low-Grade Squamous Intraepithelial Lesion; 43 High-Grade Squamous Intraepithelial Lesion and 3 (0.5 %) Invasive Cervical Cancer., Results: From the 323 samples (48.6 %) that had detectable HPV-DNA by the PapilloCheck assay, 31 were HPV negative by the cobas HPV and HC2 assays. Out of these 31 samples, 14 were associated with HR-HPVs types while the remaining 17 harbored exclusively low-risk HPVs. In contrast, 49 samples positive by cobas HPV and HC 2 methods tested negative by the PapilloCheck assay (19.8 %). Overall, the most frequent HR-HPV type was HPV 16 (23.2 %), followed by 56 (21.0 %), 52 (8.7 %) and 31 (7.7 %) and the most frequent LR-HPV type was HPV 42 (12.1 %) followed by 6 (6.2 %). Among the HR-HPV types, HPV 56 and 16 were the most frequent types in NILM, found in 19.1 and 17.7 % of the patients respectively while in HSIL and ICC cases, HPV 16 was the predominant type, detected in 37.2 and 66.7 % of these samples., Conclusions: In the population studied, HPV 16 and 56 were the most frequently detected HR-HPV types. HPV 56 was found mainly in LSIL and NILM suggesting a low oncogenic potential. HPV 16 continues to be the most prevalent type in high-grade lesions whereas HPV 18 was found in a low frequency both in NILM and abnormal smears. Surveillance of HPV infections by molecular methods is an important tool for the development and improvement of prevention strategies.
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- 2016
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25. Dementia in elderly inpatients admitted to medical wards in Brazil: diagnosis and comorbidity with other clinical diseases.
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Maia E, Steglich MS, Lima AP, Zanella Troncoso IH, da Silva KI, Martins TR, Correa Neto Y, and Lopes MA
- Subjects
- Activities of Daily Living psychology, Aged, Aged, 80 and over, Brazil epidemiology, Cognition Disorders diagnosis, Comorbidity, Delirium diagnosis, Dementia diagnosis, Dementia psychology, Depressive Disorder epidemiology, Female, Humans, Male, Middle Aged, Prevalence, Psychiatric Status Rating Scales, Risk Factors, Surveys and Questionnaires, Cognition Disorders epidemiology, Delirium epidemiology, Dementia epidemiology, Inpatients statistics & numerical data
- Abstract
Background: Specific comorbidities affect older patients with dementia admitted to general hospitals and may complicate the recognition of dementia. The aim of the present study was to estimate the prevalence of dementia among elderly inpatients admitted to hospital medical wards and to identify its distribution across clinical and sociodemographic conditions., Methods: From June 2011 to May 2012, a sample of elderly inpatients (≥60 years old) were screened for dementia with the Mini-Mental State Examination and the Bayer Activities of Daily Living Scale to identify cognitive and functional impairment (CFI). Subjects with CFI underwent a diagnostic procedure for dementia using the Cambridge Mental Disorders of the Elderly Examination and the Diagnostic and Statistical Manual of Mental Disorders, 4th edition. The elderly inpatients also completed a standard questionnaire to investigate sociodemographic and clinical variables and a screening procedure for depression and delirium. The data obtained were submitted to univariate and multivariate analyses., Results: The sample of 224 subjects had a mean age of 71.5 years and was mostly men (62.2%), poorly educated (≤4 years of schooling: 74.6%), and married (53.4%). CFI was observed in 84 subjects (prevalence: 37.4%; 95% confidence interval: 31.1-43.7), and dementia was observed in 31 subjects (prevalence: 17.2%; 95% confidence interval: 12.3-22.1). Dementia was related to older age and the presence of delirium, stroke, and pneumonia., Conclusions: The prevalence of CFI and dementia was high among the elderly inpatients examined. The identification of medical and sociodemographic conditions associated with a dementia diagnosis in a general hospital may be useful in the development of preventative actions., (© 2015 The Authors. Psychogeriatrics © 2015 Japanese Psychogeriatric Society.)
- Published
- 2016
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26. Pressure pain thresholds in patients with chronic nonspecific low back pain.
- Author
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Imamura M, Alfieri FM, Filippo TR, and Battistella LR
- Subjects
- Adolescent, Adult, Aged, Cross-Sectional Studies, Female, Humans, Low Back Pain diagnosis, Male, Middle Aged, Pressure, Surveys and Questionnaires, Young Adult, Chronic Pain physiopathology, Low Back Pain physiopathology, Muscle, Skeletal physiopathology, Pain Measurement methods, Pain Threshold physiology
- Abstract
Background: The lumbar back and hip muscles are important for a normal functioning of the human spine and they are considered to be of etiological significance in chronic nonspecific low back pain (nCLBP). Inactivity and a lower level of physical activity in patients with nCLBP may change muscle characteristics and may be associated with pain and disability. Pressure algometry has been found to be non-invasive, efficient and reliable in the exploration of physio-pathological mechanisms involved in muscle pain syndromes. The subjective characteristic of the pressure pain thresholds (PPTs) cannot be avoided once it is the very objective of the measurement, i.e. the minimum pain perceptible by the person, is a subjective factor. Most studies have revealed gender differences between PPTs, with females showing lower thresholds., Objective: to determine whether demographic variables and PPTs, are related pain intensity and a disability in patients with nCLBP., Methods: One hundred and twenty-four patients with nCLBP were included in the study. The Visual Analogue Scale (VAS) and the Roland-Morris Questionnaire for Low Back Pain (RM) were used to evaluate the intensity of pain and degree of disability. The PPT was performed from L1 up to S2 dermatomes, at the muscles over the Gluteus medius, minimus and maximus, including a point located at the level of the piriformis, at the Quadratus lumborum, at the Iliopsoas and points of reference located at the level of the L1 up to L5 ligaments. The pain intensity was assessed by visual analogue scale (VAS) and the lumbar function by Roland Morris questionnaire (RM). Multiple linear regression models were used for both the VAS and the RM., Results: No significant differences were found between the PPTs measured at either left or right limb. The mean VAS value was 7.3 (± 1.5) and the RM score was 14.2 (± 5.3). The PPT-values showed significant negative correlations to the VAS and the RM. The highest correlation between the mean VAS and PPT-values were found at the level of the Gluteus medius (r= -0.34, p< 0.001), which was the only measurement correlated to the intensity of pain (r2 = 0.11, p< 0.001). The RM was correlated to the BMI, the level of education and the PPT values at the level of the Iliopsoas muscle and the L4-L5 supraspinous ligament., Conclusions: This study showed that most PPT values are correlated to the VAS and the RM. Nevertheless, the variability explained by PPT values and demographic characteristics was low for pain intensity and function.
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- 2016
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27. Clinical characteristics of women diagnosed with carcinoma who tested positive for cervical and anal high-risk human papillomavirus DNA and E6 RNA.
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Veo CA, Saad SS, Fregnani JH, Scapulatempo-Neto C, Tsunoda AT, Resende JC, Lorenzi AT, Mafra A, Cinti C, Cotrim ID, Rosa LA, de Oliveira CM, Martins TR, Centrone C, Levi JE, and Longatto-Filho A
- Subjects
- Adult, Aged, Anal Canal pathology, Female, Gene Expression Regulation, Viral, Humans, Middle Aged, Oncogene Proteins, Viral genetics, Papillomaviridae genetics, Papillomaviridae pathogenicity, RNA, Viral genetics, RNA, Viral isolation & purification, Repressor Proteins genetics, Risk Factors, Uterine Cervical Neoplasms pathology, Uterine Cervical Neoplasms virology, Anal Canal virology, Carcinogenesis genetics, Oncogene Proteins, Viral biosynthesis, Repressor Proteins biosynthesis, Uterine Cervical Neoplasms genetics
- Abstract
High-risk human papillomavirus (hrHPV) is an essential cause of cervical carcinoma and is also strongly related to anal cancer development. The hrHPV E6 oncoprotein plays a major role in carcinogenesis. We aimed to evaluate the frequency of hrHPV DNA and E6 oncoprotein in the anuses of women with cervical carcinoma. We analyzed 117 women with cervical cancer and 103 controls for hrHPV and the E6 oncogene. Positive test results for a cervical carcinoma included 66.7 % with hrHPV-16 and 7.7 % with hrHPV-18. One case tested positive for both HPV variants (0.9 %). The samples from the anal canal were positive for HPV-16 in 59.8 % of the cases. Simultaneous presence of HPV in the cervix and anal canal was found in 53.8 % of the cases. Regarding expression of E6 RNA, positivity for HPV-16 in the anal canal was found in 21.2 % of the cases, positivity for HPV-16 in the cervix was found in 75.0 %, and positivity for HPV-18 in the cervix was found in 1.9 %. E6 expression in both the cervix and anal canal was found in 19.2 % of the cases. In the controls, 1 % tested positive for HPV-16 and 0 % for HPV-18. Anal samples from the controls showed a hrHPV frequency of 4.9 % (only HPV16). The presence of hrHPV in the anal canal of women with cervical cancer was detected at a high frequency. We also detected E6 RNA expression in the anal canal of women with cervical cancer, suggesting that these women are at risk for anal hrHPV infection.
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- 2015
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28. Variability of susceptibility to deltamethrin in peridomestic Triatoma sordida from Triângulo Mineiro, State of Minas Gerais, Brazil.
- Author
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Pessoa GC, dos Santos TR, Salazar GC, Dias LS, de Mello BV, Ferraz ML, and Diotaiuti L
- Subjects
- Animals, Biological Assay, Brazil, Chagas Disease transmission, Lethal Dose 50, Insecticides, Nitriles, Pyrethrins, Triatoma
- Abstract
Introduction: Despite chemical and physical vector control strategies, persistent infestations of Triatoma sordida have been reported in a large part of Minas Gerais, Brazil, and the cause for this is little investigated. We aimed to characterize the deltamethrin toxicological profile in peridomestic T. sordidapopulations from Triângulo Mineiro area of Minas Gerais., Methods: Susceptibility to deltamethrin was assessed in seventeen peridomestic T. sordida populations. Serial dilutions of deltamethrin in acetone (0.2µL) were topically applied on the first instar nymphs (F1; five days old; fasting weight, 1.2 ± 0.2mg). Dose response results were analyzed using Probit software, and the lethal doses, slope and resistance ratios were determined. Qualitative tests were also performed., Results: The deltamethrin susceptibility profile of T. sordida populations revealed resistance ratios ranging from 0.84 to 2.8. The percentage mortality in response to a diagnostic dose was 100.0% in all populations., Conclusions: From our results, the lack of resistance to insecticides but persistent T. sordida infestations in the Triângulo Mineiro area may be because of: 1) environmental degradation facilitating dispersion of T. sordida, allowing colonization in artificial ecotopes; 2) operational failures; and 3) complexity of the peridomicile in the study area.These variables are being investigated.
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- 2015
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29. Critical Analyses of the Introduction of Liquid-Based Cytology in a Public Health Service of the State of São Paulo, Brazil.
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Longatto-Filho A, Levi JE, Martins TR, Cohen D, Cury L, Villa LL, and Eluf-Neto J
- Subjects
- Adolescent, Adult, Aged, Brazil epidemiology, Case-Control Studies, Child, Diagnosis, Differential, Female, Follow-Up Studies, Humans, Middle Aged, Neoplasm Grading, Papanicolaou Test, Prognosis, Squamous Intraepithelial Lesions of the Cervix epidemiology, Squamous Intraepithelial Lesions of the Cervix prevention & control, United States, United States Public Health Service, Uterine Cervical Neoplasms epidemiology, Uterine Cervical Neoplasms prevention & control, Vaginal Smears, Young Adult, Uterine Cervical Dysplasia epidemiology, Uterine Cervical Dysplasia prevention & control, Atypical Squamous Cells of the Cervix pathology, Cervix Uteri pathology, Cytological Techniques methods, Squamous Intraepithelial Lesions of the Cervix diagnosis, Uterine Cervical Neoplasms diagnosis, Uterine Cervical Dysplasia diagnosis
- Abstract
Objective: The aim of this study was to compare the performance of the current conventional Pap smear with liquid-based cytology (LBC) preparations., Study Design: Women routinely undergoing their cytopathological and histopathological examinations at Fundação Oncocentro de São Paulo (FOSP) were recruited for LBC. Conventional smears were analyzed from women from other areas of the State of São Paulo with similar sociodemographic characteristics., Results: A total of 218,594 cases were analyzed, consisting of 206,999 conventional smears and 11,595 LBC. Among the conventional smears, 3.0% were of unsatisfactory preparation; conversely, unsatisfactory LBC preparations accounted for 0.3%. The ASC-H (atypical squamous cells - cannot exclude high-grade squamous intraepithelial lesion) frequency did not demonstrate any differences between the two methods. In contrast, the incidence of ASC-US (atypical squamous cells of undetermined significance) was almost twice as frequent between LBC and conventional smears, at 2.9 versus 1.6%, respectively. An equal percentage of high-grade squamous intraepithelial lesions were observed for the two methods, but not for low-grade squamous intraepithelial lesions, which were more significantly observed in LBC preparations than in conventional smears (2.2 vs. 0.7%). The index of positivity was importantly enhanced from 3.0% (conventional smears) to 5.7% (LBC)., Conclusions: LBC performed better than conventional smears, and we are truly confident that LBC can improve public health strategies aimed at reducing cervical lesions through prevention programs., (© 2015 S. Karger AG, Basel.)
- Published
- 2015
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30. Mitochondrial apoptosis-inducing factor is involved in doxorubicin-induced toxicity on H9c2 cardiomyoblasts.
- Author
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Moreira AC, Branco AF, Sampaio SF, Cunha-Oliveira T, Martins TR, Holy J, Oliveira PJ, and Sardão VA
- Subjects
- Active Transport, Cell Nucleus drug effects, Amino Acid Chloromethyl Ketones pharmacology, Animals, Antibiotics, Antineoplastic pharmacology, Apoptosis genetics, Apoptosis Inducing Factor genetics, Blotting, Western, Caspase Inhibitors pharmacology, Caspases metabolism, Cell Line, Cell Nucleus drug effects, Cell Nucleus metabolism, Cell Survival drug effects, Cell Survival genetics, DNA Fragmentation drug effects, Dose-Response Relationship, Drug, Microscopy, Confocal, Mitochondria drug effects, Mitochondria metabolism, Models, Biological, Myocytes, Cardiac cytology, Myocytes, Cardiac metabolism, RNA Interference, Rats, Time Factors, Apoptosis drug effects, Apoptosis Inducing Factor metabolism, Doxorubicin pharmacology, Myocytes, Cardiac drug effects
- Abstract
The cardiotoxicity induced by the anti-cancer doxorubicin involves increased oxidative stress, disruption of calcium homeostasis and activation of cardiomyocyte death. Nevertheless, antioxidants and caspase inhibitors often show little efficacy in preventing cell death. We hypothesize that a caspase-independent cell death mechanism with the release of the apoptosis-inducing factor from mitochondria is involved in doxorubicin toxicity. To test the hypothesis, H9c2 cardiomyoblasts were used as model for cardiac cells. Our results demonstrate that z-VAD-fmk, a pan-caspase inhibitor, does not prevent doxorubicin toxicity in this cell line. Doxorubicin treatment results in AIF translocation to the nuclei, as confirmed by Western Blotting of cell fractions and confocal microscopy. Also, doxorubicin treatment of H9c2 cardiomyoblasts resulted in the appearance of 50kbp DNA fragments, a hallmark of apoptosis-inducing factor nuclear effects. Apoptosis-inducing factor knockdown using a small-interfering RNA approach in H9c2 cells resulted in a reduction of doxorubicin toxicity, including decreased p53 activation and poly-ADP-ribose-polymerase cleavage. Among the proteases that could be responsible for apoptosis-inducing factor cleavage, doxorubicin decreased calpain activity but increased cathepsin B activation, with inhibition of the latter partly decreasing doxorubicin toxicity. Altogether, the results support that apoptosis-inducing factor release is involved in doxorubicin-induced H9c2 cell death, which explains the limited ability of caspase inhibitors to prevent toxicity., (Copyright © 2014 Elsevier B.V. All rights reserved.)
- Published
- 2014
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31. Precise spatio-temporal regulation of the anthocyanin biosynthetic pathway leads to petal spot formation in Clarkia gracilis (Onagraceae).
- Author
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Martins TR, Berg JJ, Blinka S, Rausher MD, and Baum DA
- Subjects
- Anthocyanins genetics, Chromatography, High Pressure Liquid, Crosses, Genetic, DNA, Plant chemistry, Flowers anatomy & histology, Flowers growth & development, Flowers metabolism, Genotype, Onagraceae anatomy & histology, Onagraceae growth & development, RNA, Messenger metabolism, Reverse Transcriptase Polymerase Chain Reaction, Sequence Analysis, DNA, Anthocyanins biosynthesis, Onagraceae metabolism
- Abstract
Petal spots are widespread in angiosperms and are often implicated in pollinator attraction. Clarkia gracilis petals each have a single red-purple spot that contrasts against a pink background. The position and presence of spots in C. gracilis are determined by the epistatic interaction of alleles at two as yet unidentified loci. We used HPLC to identify the different pigments produced in the petals, and qualitative and quantitative RT-PCR to assay for spatio-temporal patterns of expression of different anthocyanin pathway genes. We found that spots contain different pigments from the remainder of the petal, being composed of cyanidin/peonidin-based, instead of malvidin-based anthocyanins. Expression assays of anthocyanin pathway genes showed that the dihydroflavonol-4-reductase 2 (Dfr2) gene has a spot-specific expression pattern and acts as a switch for spot production. Co-segregation analyses implicated the gene products of the P and I loci as trans-regulators of this switch. Spot pigments appear earlier in development as a result of early expression of Dfr2 and the flavonoid 3' hydroxylase 1 (F3'h1) gene. Pigments in the background appear later, as a result of later expression of Dfr1 and the flavonoid 3'-5' hydroxylase 1 (F3'5'h1) genes. The evolution of this spot production mechanism appears to have been facilitated by duplication of the Dfr gene and to have required substantial reworking of the anthocyanin pathway regulatory network., (© 2012 The Authors. New Phytologist © 2012 New Phytologist Trust.)
- Published
- 2013
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32. Performance of RT-PCR in the detection of Streptococcus agalactiae in the anogenital tract of pregnant women.
- Author
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Feuerschuette OM, Serratine AC, Bazzo ML, Martins TR, Silveira SK, and da Silva RM
- Subjects
- Adult, Anal Canal microbiology, Antigens, Bacterial genetics, Bacteriological Techniques, Cross-Sectional Studies, DNA, Bacterial analysis, Female, Humans, Predictive Value of Tests, Pregnancy, Reproducibility of Results, Streptococcus agalactiae genetics, Vagina microbiology, Young Adult, Carrier State diagnosis, Pregnancy Complications, Infectious diagnosis, Real-Time Polymerase Chain Reaction, Streptococcal Infections diagnosis, Streptococcus agalactiae isolation & purification
- Abstract
Introduction: Infection with Group B Streptococcus (GBS) is the most frequent in the first weeks of life of a newborn. The identification of pregnant women with GBS colonization may reduce neonatal infection., Methods: This cross-sectional study evaluated the performance of real-time polymerase chain reaction (RT-PCR) to detect GBS colonization in the anogenital tract of pregnant women. Anogenital swabs were collected from 266 pregnant women from December 2010 to August 2011. GBS was detected using culture (gold standard) and RT-PCR to determine sip gene expression. The presence of DNA was confirmed using betaglobin amplification, and the guanidine technique was used for DNA extraction. When results were discordant, the test was repeated using conventional PCR. The results were evaluated to determine sensitivity, specificity, positive and negative predictive values and accuracy., Results: Of the 266 samples collected, 254 were adequate for analysis. Prevalence was 28.7% using the gold standard criterion and 38.2% using RT-PCR. The comparison of RT-PCR with culture revealed a sensitivity of 89% (95% CI 0.81-0.96), specificity of 82% (95% CI 0.76-0.87), positive predictive value of 67% (95% CI 0.57-0.76) and negative predictive value of 94% (95% CI 0.91-0.99)., Conclusion: Further studies using other DNA extraction techniques, targeting other GBS genes and using sample enhancement before RT-PCR should be conducted to determine whether the sensitivity and specificity recommended by the CDC may be reached using the same thermal cycler.
- Published
- 2012
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33. Positive selection for single amino acid change promotes substrate discrimination of a plant volatile-producing enzyme.
- Author
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Barkman TJ, Martins TR, Sutton E, and Stout JT
- Subjects
- Datura enzymology, Molecular Sequence Data, Mutagenesis, Site-Directed, Salicylic Acid metabolism, Substrate Specificity genetics, Amino Acid Substitution genetics, Datura genetics, Methyltransferases genetics, Selection, Genetic
- Abstract
We used a combined evolutionary and experimental approach to better understand enzyme functional divergence within the SABATH gene family of methyltransferases (MTs). These enzymes catalyze the formation of a variety of secondary metabolites in plants, many of which are volatiles that contribute to floral scent and plant defense such as methyl salicylate and methyl jasmonate. A phylogenetic analysis of functionally characterized members of this family showed that salicylic acid methyltransferase (SAMT) forms a monophyletic lineage of sequences found in several flowering plants. Most members of this lineage preferentially methylate salicylic acid (SA) as compared with the structurally similar substrate benzoic acid (BA). To investigate if positive selection promoted functional divergence of this lineage of enzymes, we performed a branch-sites test. This test showed statistically significant support (P<0.05) for positive selection in this lineage of MTs (dN/dS=10.8). A high posterior probability (pp=0.99) identified an active site methionine as the only site under positive selection in this lineage. To investigate the potential catalytic effect of this positively selected codon, site-directed mutagenesis was used to replace Met with the alternative amino acid (His) in a Datura wrightii floral-expressed SAMT sequence. Heterologous expression of wild-type and mutant D. wrightii SAMT in Escherichia coli showed that both enzymes could convert SA to methyl salicylate and BA to methyl benzoate. However, competitive feeding with equimolar amounts of SA and BA showed that the presence of Met in the active site of wild-type SAMT resulted in a >10-fold higher amount of methyl salicylate produced relative to methyl benzoate. The Met156His-mutant exhibited little differential preference for the 2 substrates because nearly equal amounts of methyl salicylate and methyl benzoate were produced. Evolution of the ability to discriminate between the 2 substrates by SAMT may be advantageous for efficient production of methyl salicylate, which is important for pollinator attraction as well as pathogen and herbivore defense. Because BA is a likely precursor for the biosynthesis of SA, SAMT might increase methyl salicylate levels directly by preferential methylation and indirectly by leaving more BA to be converted into SA.
- Published
- 2007
- Full Text
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