167 results on '"S., Ad"'
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2. e-Journal of Portuguese History. vol. 19, no. 2
- Author
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Fonseca, Lu��s Ad��o da, Almeida, On��simo T., Pinto, Ant��nio Costa, Cardoso, Jos�� Lu��s, Cunha, Mafalda Soares da, and Kantor, Iris
- Published
- 2021
- Full Text
- View/download PDF
3. e-Journal of Portuguese History. vol. 19, no. 1
- Author
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Fonseca, Lu��s Ad��o da, Almeida, On��simo T., Pinto, Ant��nio Costa, Cardoso, Jos�� Lu��s, Cunha, Mafalda Soares da, and Kantor, Iris
- Published
- 2021
- Full Text
- View/download PDF
4. Table of Contents
- Author
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Fonseca, Lu��s Ad��o da, Almeida, On��simo, Costa Pinto, Ant��nio, Cardoso, Jos�� Lu��s, Cunha, Mafalda Soares da, Kantor, Iris, and Jer��nimo, Miguel Bandeira
- Published
- 2021
- Full Text
- View/download PDF
5. Prospective study of inflammatory biomarkers in patients undergoing peritoneal dialysis: PO 230
- Author
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Rios, D RA, Velloso, M SS, Lima, S MA, Turani, S AD, Rodrigues, L SM, Pinheiro, M B, Dusse, L MS, Sabino, A P, Gomes, K B, and Pinto, S W
- Published
- 2013
6. Cocrystal Screening of Ibuprofen with Oxalic Acid and Citric Acid via Grinding Method
- Author
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Muhamad Fitri Othman, S. Ad Rahman, N. A. Ahmad Taifuddin, and Nornizar Anuar
- Subjects
Oxalic acid ,02 engineering and technology ,010402 general chemistry ,021001 nanoscience & nanotechnology ,01 natural sciences ,Cocrystal ,0104 chemical sciences ,Grinding ,Propanol ,Solvent ,chemistry.chemical_compound ,Differential scanning calorimetry ,chemistry ,Solubility ,Fourier transform infrared spectroscopy ,0210 nano-technology ,Nuclear chemistry - Abstract
Ibuprofen is a Class II Biological Safety Class (BSC) drugs used for relief of arthritis, as an analgesic and possesses the effect of antiplatelet. The major problem involves in ibuprofen is it has a low solubility and high permeability thus causes an unsatisfactory therapeutic effect to humans. Thus, in this work, alteration of ibuprofen's physicochemical properties is conducted by means of cocrystallization technique. Co-crystallizations of ibuprofen were prepared with selected coformers using dry grinding and liquid assisted grinding (LAG) techniques in different molar ratios while ethanol and propanol were used as a solvent. The new crystalline forms were identified and characterized by differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD) and fourier transform infrared spectroscopy (FTIR). Analysis for Ibuprofen-Citric acid (IBP-CA) system, co-crystal was successfully formed in 1:2, 1:3, 2:1 and 3:1 molar ratios for neat grinding method although the co-crystal produced is unstable. Meanwhile, for Ibuprofen-Oxalic acid (IBP-OA) system, the co-crystal formation was identified only in 1:1, 1:2 and 1:3 molar ratios for the neat grinding method. LAG method shows that co-crystal formation was unsuccessful in both solvents for IBP-CA, while IBP-OA co-crystal was formed in the molar ratio 1:1, 2:1 and 3:1 in ethanol, and 2:1 and 3:1 in propanol.
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- 2018
- Full Text
- View/download PDF
7. Arachidonic acid mediates non-capacitative calcium entry evoked by CB1-cannabinoid receptor activation in DDT1 MF-2 smooth muscle cells
- Author
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Dirk G. Demuth, M. E. Parsons, Rutger M. van Ree, E Gkoumassi, Johan Zaagsma, Bart G. J. Dekkers, Henk J. Esselink, S. Ad Nelemans, A Molleman, Melloney J. Dröge, Molecular Pharmacology, and Faculty of Science and Engineering
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STIMULATION ,medicine.medical_specialty ,Cannabinoid receptor ,Physiology ,Myocytes, Smooth Muscle ,Clinical Biochemistry ,SIGNAL-TRANSDUCTION ,Gadolinium ,Stimulation ,Electric Capacitance ,Phospholipases A ,Cell Line ,Nitric oxide ,chemistry.chemical_compound ,Receptor, Cannabinoid, CB1 ,Lanthanum ,Internal medicine ,CA2+ INFLOW SYSTEM ,medicine ,Cannabinoid receptor type 2 ,Calcium Signaling ,CANNABINOID CB1 RECEPTORS ,Arachidonic Acid ,RECIPROCAL REGULATION ,NITRIC-OXIDE ,CHANNELS ,ADENYLATE-CYCLASE ,Cell Biology ,Anandamide ,2-AMINOETHOXYDIPHENYL BORATE ,Phospholipases A2 ,Endocrinology ,ANANDAMIDE ,chemistry ,Capacitative calcium entry ,Calcium ,Arachidonic acid ,Mitogen-Activated Protein Kinases ,Signal transduction ,Histamine - Abstract
Cannabinoid CB1-receptor stimulation in DDT1 MF-2 smooth muscle cells induces a rise in [Ca2+](i), which is dependent on extracellular Ca2+ and modulated by thapsigargin-sensitive stores, suggesting capacitative Ca2+ entry (CCE), and by MAP kinase. Non-capacitative Ca2+ entry (NCCE) stimulated by arachidonic acid (AA) partly mediates histamine H-1-receptor-evoked increases in [Ca2+](i) in DDT1 MF-2 cells. In the current study, both Ca2+ entry mechanisms and a possible link between MAP kinase activation and increasing [Ca2+](i) were investigated. In the whole-cell patch clamp configuration, the CB-receptor agonist CP 55, 940 evoked a transient, Ca2+-dependent K+ current, which was not blocked by the inhibitors of CCE, 2-APB, and SKF 96365. AA, but not its metabolites, evoked a transient outward current and inhibited the response to CP 55,940 in a concentration-dependent manner. CP 55,940 induced a concentration-dependent release of AA, which was inhibited by the CB1 antagonist SR141716. The non-selective Ca2+ channel blockers La3+ and Gd3+ inhibited the CP 55,940-induced at concentrations that had no effect on thapsigargin-evoked CCE. La3+ also inhibited the AA-induced current. CP 55,940-induced AA release was abolished by Gd3+ and by phospholipase A(2) inhibition using quinacrine; this compound also inhibited the outward current. The CP 55,940-induced AA release was strongly reduced by the MAP kinase inhibitor PD 98059. The data suggest that in DDT1 MF-2 cells, AA is an integral component of the CB1 receptor signaling pathway, upstream of NCCE and, via PLA(2), downstream of MAP kinase.
- Published
- 2005
8. A Geometric Approach to the Landauer-B��ttiker Formula
- Author
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S��ad, R. Ben and Pillet, C. -A.
- Subjects
Statistical Mechanics (cond-mat.stat-mech) ,FOS: Physical sciences ,Mathematical Physics (math-ph) ,Quantum Physics (quant-ph) - Abstract
We consider an ideal Fermi gas confined to a geometric structure consisting of a central region -- the sample -- connected to several infinitely extended ends -- the reservoirs. Under physically reasonable assumptions on the propagation properties of the one-particle dynamics within these reservoirs, we show that the state of the Fermi gas relaxes to a steady state. We compute the expected value of various current observables in this steady state and express the result in terms of scattering data, thus obtaining a geometric version of the celebrated Landauer-B��ttiker formula.
- Published
- 2014
- Full Text
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9. Emulsion sheet doublets as interface trackers for the OPERA experiment
- Author
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Anokhina, A. w, Aoki, S. q, Ariga, A. y, Arrabito, L. s, Autiero, D. s, Badertscher, A. al, Bay, F. a, Greggio, F. G. ai, Bertolin, A. ad, Besnier, M. b, Bick, D. n, Bozza, C. ag, Brugiere, T. s, Brugnera, R. ae, Brunetti, G. h, Buontempo, S. z, Carrara, E. ae, Cazes, A. k, Chaussard, L. s, Chernyavsky, M. v, Chiarella, V. k, Chon Sen, N. ah, Chukanov, A. z, Consiglio, L. h, Cozzi, M. h, Cuha, V. a, Dal Corso, F. ad, D'Amato, G. ag, D'Ambrosio, N. c, De Lellis, G. aa, Déclais, Y. s, De Serio, M. e, z, Di Ferdinando, D. g, Di Giovanni, A. r, Di Marco, N. r, Di Troia, C. k, Dmitrievski, S. j, Dominjon, A. s, Dracos, M. ah, Duchesneau, D. b, Dusini, S. ad, Ebert, J. n, Egorov, O. u, Enikeev, R. t, Ereditato, A. f, Esposito, L. S. c, Favier, J. b, Felici, G. k, Ferber, T. n, Fini, R. e, Frekers, D. x, Fukuda, T. y, Galkin, V. I. w, Galkin, V. A. ac, Garfagnini, A. ae, Giacomelli, G. h, Giorgini, M. h, Goellnitz, C. n, Goldberg, J. m, Golubkov, D. u, Gornushkin, Y. j, Grella, Grianti, F. ai, Guler, M. a, Gusev, G. v, Gustavino, C. c, Hagner, C. n, Hara, T. q, Hierholzer, M. n, Hiramatsu, S. y, Hoshino, K. y, Ieva, M. e, Jakovcic, K. ak, Janicsko Csathy, J. ab, Janutta, B. n, Jollet, C. ah, Juget, F. ab, Kawai, T. y, Kazuyama, M. y, Kim, S. H. oam, Knuesel, J. f, Kodama, K. p, Komatsu, M. y, Kose, U. a, Kreslo, I. f, Laktineh, I. s, Lazzaro, C. al, Lenkeit, J. n, Ljubicic, A. ak, Longhin, Lutter, G. ab, Manai, K. s, Mandrioli, G. g, Marotta, A. z, Marteau, J. s, Matsuo, T. l, Matsuoka, H. y, Mauri, N. h, Meisel, Meregaglia, A. ah, Messina, M. f, Migliozzi, P. z, Mikado, S. lan, Miyamoto, S. y, Monacelli, P. r, Morishima, K. y, Moser, U. f, Muciaccia, M. T. d, Naganawa, N. y, Naka, T. y, Nakamura, M. y, Nakamura, T. y, Nakano, T. y, Nikitina, V. w, Niwa, K. y, Nonoyama, Y. y, Ogawa, S. l, Osedlo, V. w, Ossetski, D. ac, Paoloni, A. k, Park, B. D. o, Park, I. G. o, Pastore, A. d, Patrizii, L. g, Pennacchio, E. s, Pessard, H. b, Pilipenko, V. x, Pistillo, C. f, Polukhina, N. v, Pozzato, M. h, Pretzl, K. f, Publichenko, P. w, Pupilli, F. r, Roganova, T. w, Rosa, G. af, Rostovtseva, I. u, Rubbia, Russo, A. z, Ryazhskaya, O. t, Ryzhikov, Sato, O. y, Sato, Y. aj, Saveliev, V. ac, Sazhina, G. w, Schembri, A. c, Scotto Lavina, L. z, Shibuya, H. l, Simone, S. d, Sioli, M. h, Sirignano, Sirri, G. g, Song, J. S. o, Spinetti, M. k, Stanco, L. ad, Starkov, N. v, Stipcevic, M. ak, Strauss, T. al, Strolin, P. aa, Sugonyaev, V. ad, Taira, Y. y, Takahashi, S. y, Tenti, M. h, Terranova, F. k, Tezuka, I. aj, Tioukov, V. z, Tolun, P. a, Tsarev, V. v, Tufanli, S. a, Ushida, N. p, Vilain, P. i, Vladimirov, M. v, Votano, L. k, Vuilleumier, J. L. ab, Wilquet, G. i, Wonsak, B. n, Yoon, C. S. o, Yoshida, J. y, Zaitsev, Y. u, Zemskova, S. j, Zghiche, A. b, Zimmermann, R. n., DI CAPUA, FRANCESCO, Anokhina, A. w, Aoki, S. q, Ariga, A. y, Arrabito, L., Autiero, D., Badertscher, A., Al, Bay, F. a, Greggio, F. G., Ai, Bertolin, A., Ad, Besnier, M. b, Bick, D. n, Bozza, C., Ag, Brugiere, T., Brugnera, R., Ae, Brunetti, G. h, Buontempo, S. z, Carrara, E., Ae, Cazes, A. k, Chaussard, L., Chernyavsky, M. v, Chiarella, V. k, Chon, Sen, N., Ah, Chukanov, A. z, Consiglio, L. h, Cozzi, M. h, Cuha, V. a, Dal, Corso, F., Ad, D'Amato, G., Ag, D'Ambrosio, N. c, De, Lelli, G., Aa, Déclais, Y., De, Serio, M., E., DI CAPUA, Francesco, Z, Di, Ferdinando, D., G., Di, Giovanni, A., R., Di, Marco, N., R., Di, Troia, C. k, Dmitrievski, S. j, Dominjon, A. s, Draco, M., Ah, Duchesneau, D. b, Dusini, S., Ad, Ebert, J. n, Egorov, O. u, Enikeev, R. t, Ereditato, A. f, Esposito, L. S. c, Favier, J. b, Felici, G. k, Ferber, T. n, Fini, R. e, Frekers, D. x, Fukuda, T. y, Galkin, V. I. w, Galkin, V. A., Ac, Garfagnini, A., Ae, Giacomelli, G. h, Giorgini, M. h, Goellnitz, C. n, Goldberg, J. m, Golubkov, D. u, Gornushkin, Y. j, Grella, Grianti, F., Ai, Guler, M. a, Gusev, G. v, Gustavino, C. c, Hagner, C. n, Hara, T. q, Hierholzer, M. n, Hiramatsu, S. y, Hoshino, K. y, Ieva, M. e, Jakovcic, K., Ak, Janicsko, Csathy, J., Ab, Janutta, B. n, Jollet, C., Ah, Juget, F., Ab, Kawai, T. y, Kazuyama, M. y, Kim, S. H., Oam, Knuesel, J. f, Kodama, K. p, Komatsu, M. y, Kose, U. a, Kreslo, I. f, Laktineh, I., Lazzaro, C., Al, Lenkeit, J. n, Ljubicic, A., Ak, Longhin, Lutter, G., Ab, Manai, K., Mandrioli, G. g, Marotta, A. z, Marteau, J., Matsuo, T. l, Matsuoka, H. y, Mauri, N. h, Meisel, Meregaglia, A., Ah, Messina, M. f, Migliozzi, P. z, Mikado, S., Lan, Miyamoto, S. y, Monacelli, P. r, Morishima, K. y, Moser, U. f, Muciaccia, M. T. d, Naganawa, N. y, Naka, T. y, Nakamura, M. y, Nakamura, T. y, Nakano, T. y, Nikitina, V. w, Niwa, K. y, Nonoyama, Y. y, Ogawa, S. l, Osedlo, V. w, Ossetski, D., Ac, Paoloni, A. k, Park, B. D. o, Park, I. G. o, Pastore, A. d, Patrizii, L. g, Pennacchio, E., Pessard, H. b, Pilipenko, V. x, Pistillo, C. f, Polukhina, N. v, Pozzato, M. h, Pretzl, K. f, Publichenko, P. w, Pupilli, F. r, Roganova, T. w, Rosa, G., Af, Rostovtseva, I. u, Rubbia, Russo, A. z, Ryazhskaya, O. t, Ryzhikov, Sato, O. y, Sato, Y., Aj, Saveliev, V., Ac, Sazhina, G. w, Schembri, A. c, Scotto, Lavina, L. z, Shibuya, H. l, Simone, S. d, Sioli, M. h, Sirignano, Sirri, G. g, Song, J. S. o, Spinetti, M. k, Stanco, L., Ad, Starkov, N. v, Stipcevic, M., Ak, Strauss, T., Al, Strolin, P., Aa, Sugonyaev, V., Ad, Taira, Y. y, Takahashi, S. y, Tenti, M. h, Terranova, F. k, Tezuka, I., Aj, Tioukov, V. z, Tolun, P. a, Tsarev, V. v, Tufanli, S. a, Ushida, N. p, Vilain, P. i, Vladimirov, M. v, Votano, L. k, Vuilleumier, J. L., Ab, Wilquet, G. i, Wonsak, B. n, Yoon, C. S. o, Yoshida, J. y, Zaitsev, Y. u, Zemskova, S. j, Zghiche, A. b, and Zimmermann, R. n.
- Subjects
Detector alignment and calibration methods (Lasers,Sources,Particle-beams) ,Detector design and construction technologies and material ,Particle tracking detectors ,Large detector systems for particle and astroparticle physic - Abstract
New methods for efficient and unambiguous interconnection between electronic position sensitive detectors and target units based on nuclear photographic emulsion films have been developed. The application to the OPERA experiment,that aims at detecting Vμ⇋Vτoscillations in the CNGS neutrino beam,is reported in this paper. In order to reduce background due to latent tracks collected before installation in the detector,on-site large-scale treatments of the emulsions (“refreshing”) have been applied. Changeable Sheet (CSd) packages,each made of a doublet of emulsion films,have been designed,assembled and coupled to the OPERA target units (“ECC bricks”). A device has been built to print X-ray spots for accurate interconnection both within the CSd and between the CSd and the related ECC brick. Sample emulsion films have been extensively scanned with state-of-the-art automated optical microscopes. Efficient track-matching and powerful background rejection have been achieved in tests with electronically tagged penetrating muons. Further improvement of in-doublet film alignment was obtained by matching the pattern of low-energy electron tracks. The commissioning of the overall OPERA alignment procedure is in progress.
- Published
- 2008
10. Hydrozoan species richness in the Mediterranean Sea: past and present
- Author
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Gravili, C. ad, Di Camillo, C.G. b, Piraino, S. ad, Boero, F. acd, Gravili, Cinzia, Cristina Gioia Di, Camillo, Piraino, Stefano, and Boero, Ferdinando
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0106 biological sciences ,Mediterranean climate ,Extinction ,Ecology ,species diversity ,Range (biology) ,010604 marine biology & hydrobiology ,Fauna ,Introduced species ,Aquatic Science ,Biology ,010603 evolutionary biology ,01 natural sciences ,Mediterranean sea ,Hydrozoa ,Zoogeography ,Mediterranean Sea fauna ,14. Life underwater ,Species richness ,Ecology, Evolution, Behavior and Systematics ,benthos ,new species ,range expansion ,species richness ,taxonomy ,zoogeography - Abstract
The Mediterranean hydrozoan fauna (Siphonophora excluded) comprises 400 species; most (68%) occur in the Atlantic Ocean, 20% are endemic to the Mediterranean, 8% are of Indo-Pacific origin, and 4% are non-classifiable. There are 69 nonindigenous (NIS) species in the basin: 44% of these are casual (recorded just one or very few times), 28% established (widely recorded in the basin), 6% invasive (established NIS that are able rapidly or largely to disseminate away from the area of initial introduction, having a noticeable impact on the recipient community), and 22% questionable (of doubtful taxonomic status). Entry through the Suez Canal and range expansion through the Gibraltar Strait, often enhanced by ship traffic, appear to be the main processes for recent species introductions, but uncertainties remain for many NIS. Species additions immediately result in larger local or regional species pools, but the newcomers might impact on populations of native species, altering extinction probabilities. A more reliable evaluation of the species pool can be accomplished by adding new species when they enter the taxonomic record (i.e. the records of any taxon in all types of literature), and by removing species that have not been found for a 'reasonable' time (e.g. several decades). Of the 400 non-siphonophoran hydrozoan species known to occur in the Mediterranean Sea, positive records in the last 10 years are available for 156 species (39%), whereas records of the remaining 244 species are older than a decade: 67 species have not been recorded for 41 years, 13 for 31-40 years, 79 for 21-30 years, and 85 for 11-20 years. © 2013 Blackwell Verlag GmbH.
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- 2013
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11. Innesto di 'graft' autologo nel trattamento del 'buried penis' dopo circoncisione
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A. s. i. m. a. k. o. p. o. u. l. o. s., Ad, Iorio, B, Casilio, M, and Spera, E
- Subjects
Settore MED/24 - Urologia - Published
- 2011
12. Two Archaic Poetic Compositions in Soqotri: 1905-1981-2012
- Author
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Naumkin, V., primary, Kogan, L., additional, Cherkashin, D., additional, s ad-Da rh , A., additional, and Ad-Da rh , sa G., additional
- Published
- 2014
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13. Arachidonic acid mediates non-capacitative calcium entry evoked by CB1-cannabinoid receptor activation in DDT1 MF-2 smooth muscle cells
- Author
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Demuth, Dirk G., primary, Gkoumassi, Effimia, additional, Dröge, Melloney J., additional, Dekkers, Bart G.J., additional, Esselink, Henk J., additional, van Ree, Rutger M., additional, Parsons, Mike E., additional, Zaagsma, Johan, additional, Molleman, Areles, additional, and Nelemans, S. Ad, additional
- Published
- 2005
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14. CᵊMIYYᵊTIN SOSIAL STRUKTURU HAQQINDA NᵊZᵊRIYYᵊLᵊR.
- Author
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MᵊMMᵊDOVA, Sᵊad ᵊt Davud Q.
- Abstract
Copyright of Electronic Turkish Studies is the property of Electronic Turkish Studies and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2014
15. Microviscosity changes during differentiation of neuroblastoma cells
- Author
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Meir Shinitzky, Siegfried W. de Laat, Paul T. Van Der Saag, and S. Ad Nelemans
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Viscosity ,Vesicle ,Cell Membrane ,Dipalmitoyl Phosphatidylcholine ,Temperature ,Biophysics ,Cell Differentiation ,Cell Biology ,Metabolism ,Biology ,Mouse Neuroblastoma ,Biochemistry ,Fluorescence ,Cell Line ,Cell biology ,Microviscosity ,Neuroblastoma cell ,Neuroblastoma ,Spectrometry, Fluorescence ,Membrane fluidity ,Microscopy, Phase-Contrast - Abstract
Microviscosity η of the plasma-membrane lipid matrix was measured in exponentially growing and differentiating C1300 mouse neuroblastoma cells, attached to a glass substratum, by fluorescence polarisation of 1,6-diphenyl-1,3,5-hexatriene. Upon differentiation η decreases progressively, reaching values below those observed in the growth phase. Treatment of the cells with dipalmitoyl phosphatidylcholine vesicles reversibly inhibits morphological differentiation. The results show that a high membrane fluidity is a prerequisite for differentiation.
- Published
- 1978
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16. The distribution of phosphatidylinositol in microsomal membranes from rat liver after biosynthesis de novo. Evidence for the existence of different pools of microsomal phosphatidylinositol by the use of phosphatidylinositol-exchange protein
- Author
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Peter H. Burbach, Jan Westerman, Karel W. A. Wirtz, S. Ad Nelemans, Peter J. Brophy, and Laurens L. M. Van Deenen
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History ,Phospholipid ,Biology ,Computer Science Applications ,Education ,chemistry.chemical_compound ,Membrane ,chemistry ,Membrane protein ,Biochemistry ,Biosynthesis ,Cytoplasm ,Microsome ,Inositol ,Phosphatidylinositol - Abstract
1. The phosphatidylinositol-exchange protein from bovine brain was used to determine to what extent phosphatidylinositol in rat liver microsomal membranes is available for transfer. 2. The microsomal membranes used in the transfer reaction contained either phosphatidyl[2-3H]inositol or 32P-labelled phospholipid. The 32P-labelled microsomal membranes were isolated from rat liver after an intraperitoneal injection of [32P]Pi. The 3H-labelled microsomal membranes and rough- and smooth-endoplasmic-reticulum membranes were prepared in vitro by the incorporation of myo-[2-3H]inositol into phosphatidylinositol by either exchange in the presence of Mn2+ or biosynthesis de novo in the presence of CTP and Mg2+. 3. Tryptic or chymotryptic treatment of the microsomes impaired the biosynthesis de novo of phosphatidylinositol. It was therefore concluded that the biosynthesis of phosphatidylinositol and/or its immediate precursor CDP-diacylglycerol takes place on the cytoplasmic surface of the microsomal membrane. 4. Under the conditions of incubation 42% of the microsomal phosphatidyl[2-3H]inositol was transferred with an estimated half-life of 5min; 38% was transferred with an estimated half-life of about 1h; the remaining 20% was not transferable. Identical results were obtained irrespective of the method of myo-[2-3H]inositol incorporation. 5. Both measurement of phosphatidylinositol phosphorus in the microsomes after transfer and the transfer of microsomal [32P]phosphatidylinositol indicate that phosphatidyl[2-3H]-inositol formed by exchange or biosynthesis de novo was homogeneously distributed throughout the microsomal phosphatidylinositol. 6. We present evidence that the slowly transferable pool of phosphatidylinositol does not represent the luminal side of the microsomal membrane; hence we suggest that this phosphatidylinositol is bound to membrane proteins.
- Published
- 1978
- Full Text
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17. The distribution of phosphatidylinositol in microsomal membranes from rat liver after biosynthesis de novo. Evidence for the existence of different pools of microsomal phosphatidylinositol by the use of phosphatidylinositol-exchange protein
- Author
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Brophy, Peter J., Burbach, Peter, Nelemans, S. Ad, Westerman, Jan, Wirtz, Karel W. A., and Van Deenen, Laurens L. M.
- Abstract
1. The phosphatidylinositol-exchange protein from bovine brain was used to determine to what extent phosphatidylinositol in rat liver microsomal membranes is available for transfer. 2. The microsomal membranes used in the transfer reaction contained either phosphatidyl[2-3H]inositol or 32P-labelled phospholipid. The 32P-labelled microsomal membranes were isolated from rat liver after an intraperitoneal injection of [32P]Pi. The 3H-labelled microsomal membranes and rough- and smooth-endoplasmic-reticulum membranes were prepared in vitro by the incorporation of myo-[2-3H]inositol into phosphatidylinositol by either exchange in the presence of Mn2+ or biosynthesis de novo in the presence of CTP and Mg2+. 3. Tryptic or chymotryptic treatment of the microsomes impaired the biosynthesis de novo of phosphatidylinositol. It was therefore concluded that the biosynthesis of phosphatidylinositol and/or its immediate precursor CDP-diacylglycerol takes place on the cytoplasmic surface of the microsomal membrane. 4. Under the conditions of incubation 42% of the microsomal phosphatidyl[2-3H]inositol was transferred with an estimated half-life of 5min; 38% was transferred with an estimated half-life of about 1h; the remaining 20% was not transferable. Identical results were obtained irrespective of the method of myo-[2-3H]inositol incorporation. 5. Both measurement of phosphatidylinositol phosphorus in the microsomes after transfer and the transfer of microsomal [32P]phosphatidylinositol indicate that phosphatidyl[2-3H]-inositol formed by exchange or biosynthesis de novo was homogeneously distributed throughout the microsomal phosphatidylinositol. 6. We present evidence that the slowly transferable pool of phosphatidylinositol does not represent the luminal side of the microsomal membrane; hence we suggest that this phosphatidylinositol is bound to membrane proteins.
- Published
- 1978
- Full Text
- View/download PDF
18. Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing
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Kunkle, BW, Grenier-Boley, B, Sims, R, Bis, JC, Naj, AC, Boland, A, Vronskaya, M, Van Der Lee, SJ, Amlie-Wolf, A, Bellenguez, C, Frizatti, A, Chouraki, V, Martin, ER, Sleegers, K, Badarinarayan, N, Jakobsdottir, J, Hamilton-Nelson, KL, Aloso, R, Raybould, R, Chen, Y, Kuzma, AB, Hiltunen, M, Morgan, T, Ahmad, S, Vardarajan, BN, Epelbaum, J, Hoffmann, P, Boada, M, Beecham, GW, Garnier, JG, Harold, D, Fitzpatrick, AL, Valladares, O, Moutet, ML, Gerrish, A, Smith, AV, Qu, L, Bacq, D, Denning, N, Jian, X, Zhao, Y, Zompo, MD, Fox, NC, Grove, ML, Choi, SH, Mateo, I, Hughes, JT, Adams, HH, Malamon, J, Garcia, FS, Patel, Y, Brody, JA, Dombroski, B, Naranjo, MCD, Daniilidou, M, Eiriksdottir, G, Mukherjee, S, Wallon, D, Uphill, J, Aspelund, T, Cantwell, LB, Garzia, F, Galimberti, D, Hofer, E, Butkiewics, M, Fin, B, Scarpini, E, Sarnowski, C, Bush, W, Meslage, S, Kornhuber, J, White, CC, Song, Y, Barber, RC, Engelborghs, S, Pichler, S, Voijnovic, D, Adams, PM, Vandenberghe, R, Mayhaus, M, Cupples, LA, Albert, MS, De Deyn, PP, Gu, W, Himali, JJ, Beekly, D, Squassina, A, Hartmann, AM, Orellana, A, Blacker, D, Rodriguez-Rodriguez, E, Lovestone, S, Garcia, ME, Doody, RS, Fernadez, CM, Sussams, R, Lin, H, Fairchild, TJ, Benito, YA, Holmes, C, Comic, H, Frosch, MP, Thonberg, H, Maier, W, Roschupkin, G, Ghetti, B, Giedraitis, V, Kawalia, A, Li, S, Huebinger, RM, Kilander, L, Moebus, S, Hernández, I, Kamboh, MI, Brundin, R, Turton, J, Yang, Q, Katz, MJ, Concari, L, Lord, J, Beiser, AS, Keene, CD, Helisalmi, S, Kloszewska, I, Kukull, WA, Koivisto, AM, Lynch, A, Tarraga, L, Larson, EB, Haapasalo, A, Lawlor, B, Mosley, TH, Lipton, RB, Solfrizzi, V, Gill, M, Longstreth, WT, Montine, TJ, Frisardi, V, Ortega-Cubero, S, Rivadeneira, F, Petersen, RC, Deramecourt, V, Ciaramella, A, Boerwinkle, E, Reiman, EM, Fievet, N, Caltagirone, C, Rotter, JI, Reisch, JS, Hanon, O, Cupidi, C, Uitterlinden, AG, Royall, DR, Dufouil, C, Maletta, RG, Moreno-Grau, S, Sano, M, Brice, A, Cecchetti, R, St George-Hyslop, P, Ritchie, K, Tsolaki, M, Tsuang, DW, Dubois, B, Craig, D, Wu, CK, Soininen, H, Avramidou, D, Albin, RL, Fratiglioni, L, Germanou, A, Apostolova, LG, Keller, L, Koutroumani, M, Arnold, SE, Panza, F, Gkatzima, O, Asthana, S, Hannequin, D, Whitehead, P, Atwood, CS, Caffarra, P, Hampel, H, Baldwin, CT, Lannfelt, L, Rubinsztein, DC, Barnes, LL, Pasquier, F, Frölich, L, Barral, S, McGuinness, B, Beach, TG, Johnston, JI, Becker, JT, Passmore, P, Bigio, EH, Schott, JM, Bird, TD, Warren, JD, Boeve, BF, Lupton, MK, Bowen, JD, Proitsi, P, Boxer, A, Powell, JF, Burke, Kauwe, JK, Burns, JM, Mancuso, M, Buxbaum, JD, Bonuccelli, U, Cairns, NJ, McQuillin, A, Cao, C, Livingston, G, Carlson, CS, Bass, NJ, Carlsson, CM, Hardy, J, Carney, RM, Bras, J, Carrasquillo, MM, Guerreiro, R, Allen, M, Chui, HC, Fisher, E, Cribbs, DH, Masullo, C, Crocco, EA, DeCarli, C, Bisceglio, G, Dick, M, Ma, L, Duara, R, Graff-Radford, NR, Evans, DA, Hodges, A, Faber, KM, Scherer, M, Fallon, KB, Riemenschneider, M, Fardo, DW, Heun, R, Farlow, MR, Ferris, S, Leber, M, Foroud, TM, Heuser, I, Galasko, DR, Giegling, I, Gearing, M, Hüll, M, Geschwind, DH, Gilbert, Morris, J, Green, RC, Mayo, K, Growdon, JH, Feulner, T, Hamilton, RL, Harrell, LE, Drichel, D, Honig, LS, Cushion, TD, Huentelman, MJ, Hollingworth, P, Hulette, CM, Hyman, BT, Marshall, R, Jarvik, GP, Meggy, A, Abner, E, Menzies, G, Jin, LW, Leonenko, G, Jun, G, Grozeva, D, Karydas, A, Russo, G, Kaye, JA, Kim, R, Jessen, F, Kowall, NW, Vellas, B, Kramer, JH, Vardy, E, LaFerla, FM, Jöckel, KH, Lah, JJ, Dichgans, M, Leverenz, JB, Mann, D, Levey, AI, Pickering-Brown, S, Lieberman, AP, Klopp, N, Lunetta, KL, Wichmann, HE, Lyketsos, CG, Morgan, K, Marson, DC, Brown, K, Martiniuk, F, Medway, C, Mash, DC, Nöthen, MM, Masliah, E, Hooper, NM, McCormick, WC, Daniele, A, McCurry, SM, Bayer, A, McDavid, AN, Gallacher, J, McKee, AC, Van Den Bussche, H, Mesulam, M, Brayne, C, Miller, BL, Riedel-Heller, S, Miller, CA, Miller, JW, Al-Chalabi, A, Morris, JC, Shaw, CE, Myers, AJ, Wiltfang, J, O’Bryant, S, Coto, E, Olichney, JM, Alvarez, V, Parisi, JE, Singleton, AB, Paulson, HL, Collinge, J, Perry, W, Mead, S, Peskind, E, Rosser, M, Pierce, A, Ryan, N, Poon, WW, Nacmias, B, Potter, H, Sorbi, S, Quinn, JF, Sacchinelli, E, Raj, A, Spalletta, G, Raskind, M, Bossù, P, Reisberg, B, Clarke, R, Reitz, C, and S, AD
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2 Aetiology ,Aging ,Prevention ,Human Genome ,4202 Epidemiology ,42 Health Sciences ,Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) ,Neurodegenerative ,3101 Biochemistry and Cell Biology ,Alzheimer's Disease ,3105 Genetics ,3. Good health ,Brain Disorders ,Clinical Research ,FOS: Biological sciences ,Neurological ,Acquired Cognitive Impairment ,Genetics ,2.1 Biological and endogenous factors ,Dementia ,31 Biological Sciences - Abstract
Introduction Late-onset Alzheimer’s disease (LOAD, onset age > 60 years) is the most prevalent dementia in the elderly 1 , and risk is partially driven by genetics 2 . Many of the loci responsible for this genetic risk were identified by genome-wide association studies (GWAS) 3–8 . To identify additional LOAD risk loci, the we performed the largest GWAS to date (89,769 individuals), analyzing both common and rare variants. We confirm 20 previous LOAD risk loci and identify four new genome-wide loci ( IQCK , ACE , ADAM10 , and ADAMTS1 ). Pathway analysis of these data implicates the immune system and lipid metabolism, and for the first time tau binding proteins and APP metabolism. These findings show that genetic variants affecting APP and Aβ processing are not only associated with early-onset autosomal dominant AD but also with LOAD. Analysis of AD risk genes and pathways show enrichment for rare variants ( P = 1.32 × 10 −7 ) indicating that additional rare variants remain to be identified.
19. Fibrin Substrate Supports Chondrogenesis of Adipose-Derived Stem Cells Supplemented by Human Platelet-Rich Plasma and L-Ascorbic Acid 2-Phosphate
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K. Fernandi Moegni, S. Ad, Iis Rosliana, Siti Sobariah, Irsyah Afini, Komang Ardi Wahyuningsih, Wismo Reja Subroto, Imam Rosadi, and Tias Widyastuti
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Cancer Research ,Transplantation ,biology ,Chemistry ,Immunology ,Cell Biology ,Chondrogenesis ,Fibrin ,Glycosaminoglycan ,Andrology ,Red blood cell ,medicine.anatomical_structure ,Oncology ,White blood cell ,biology.protein ,medicine ,Immunology and Allergy ,Platelet ,Platelet activation ,Genetics (clinical) ,Fetal bovine serum - Abstract
Background & Aim Cartilage engineering study is globally rising nowadays to overcome the need of cartilage tissue. Induced chondrogenesis of adipose-derived stem cells (ADSCs) supplemented by platelet-rich plasma (PRP) or L-ascorbic acid 2-phosphate (LAA2P) has been reported. The PRP contains TGF-β to induce chondrogenesis while LAA2P induced chondrogenesis through sodium vitamin C transporter 2 (SCVT-2). Type 2 collagen (T2Col) is chondrogenesis marker and type 1 collagen (T1Col) is osteogenesis marker. However, the use of fibrin clot PRP as a substrate for chondrogenesis is still lack of data. This research aimed to study chondrogenesis of ADSCs supplemented by 10% PRP or LAA2P (50µg/mL) with fibrin as substrate. Methods, Results & Conclusion The ADSCs was isolated from human lipoaspirates while PRP was isolated from human blood. The fibrin clot substrate was fabricated trough platelet activation as a waste form. The characteristic of ADSCs, PRP composition and wet weight of fibrin substrate were conducted. Then, the ADSCs cultured in fibrin substrate with different groups of supplementation which were 10% fetal bovine serum (FBS), 10% PRP, and combination of 10%FBS-LAA2P (50µg/mL). Chondrogenesis of ADSCs on day 12 were evaluated by glycosaminoglycans (GAG) and gene expression of T2Col and T1Col. The results showed that the cell was fibroblast-like shape with the viability more than 85% and the doubling time about 2.1 days. The PRP contains highest level of platelet but lack of red blood cell (RBC), white blood cell (WBC), lymphocyte and neutrophils. The GAG value of PRP and LAA2P groups were higher than FBS group. Furthermore, the T2Col and T1Col expression of PRP was significantly higher (p
20. Léonora, traduction de l'anglais (d'après l'allemand de Bürger, par W. R. Spencer, et en français) par S.-Ad. de La Madelaine
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La Madelaine, S.-Ad. de. Traducteur, Bürger, Gottfried August (1747-1794). Auteur du texte, La Madelaine, S.-Ad. de. Traducteur, and Bürger, Gottfried August (1747-1794). Auteur du texte
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Avec mode texte
21. Léonora, traduction de l'anglais (d'après l'allemand de Bürger, par W. R. Spencer, et en français) par S.-Ad. de La Madelaine
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La Madelaine, S.-Ad. de. Traducteur, Bürger, Gottfried August (1747-1794). Auteur du texte, La Madelaine, S.-Ad. de. Traducteur, and Bürger, Gottfried August (1747-1794). Auteur du texte
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Avec mode texte
22. Cocrystal Screening of Ibuprofen with Oxalic Acid and Citric Acid via Grinding Method.
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M F Othman, N Anuar, S Ad Rahman, and N A Ahmad Taifuddin
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- 2018
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23. SYNCHRONISATION OF CELL PHASE IN TREATMENT OF LEUKÆMIA
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Al-Ismail S. Ad, J.A. Whittaker, and M. Khurshid
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Adult ,Male ,Adolescent ,business.industry ,Cytological Techniques ,Cytarabine ,General Medicine ,Middle Aged ,S Phase ,Cell phase ,Cell biology ,Leukemia, Myeloid, Acute ,Doxorubicin ,Antineoplastic Combined Chemotherapy Protocols ,Humans ,Medicine ,Female ,business ,Aged - Published
- 1977
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24. Cocrystal Screening of Ibuprofen with Oxalic Acid and Citric Acid via Grinding Method
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Othman, M F, Anuar, N, Rahman, S Ad, and Ahmad, N A
- Abstract
Ibuprofen is a Class II Biological Safety Class (BSC) drugs used for relief of arthritis, as an analgesic and possesses the effect of antiplatelet. The major problem involves in ibuprofen is it has a low solubility and high permeability thus causes an unsatisfactory therapeutic effect to humans. Thus, in this work, alteration of ibuprofen's physicochemical properties is conducted by means of cocrystallization technique. Co-crystallizations of ibuprofen were prepared with selected coformers using dry grinding and liquid assisted grinding (LAG) techniques in different molar ratios while ethanol and propanol were used as a solvent. The new crystalline forms were identified and characterized by differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD) and fourier transform infrared spectroscopy (FTIR). Analysis for Ibuprofen-Citric acid (IBP-CA) system, co-crystal was successfully formed in 1:2, 1:3, 2:1 and 3:1 molar ratios for neat grinding method although the co-crystal produced is unstable. Meanwhile, for Ibuprofen-Oxalic acid (IBP-OA) system, the co-crystal formation was identified only in 1:1, 1:2 and 1:3 molar ratios for the neat grinding method. LAG method shows that co-crystal formation was unsuccessful in both solvents for IBP-CA, while IBP-OA co-crystal was formed in the molar ratio 1:1, 2:1 and 3:1 in ethanol, and 2:1 and 3:1 in propanol.
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- 2018
25. Missing mass spectra in hadronic events from e +e −collisions at [formula omitted] 161–172 GeV and limits on invisible Higgs decays
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Acciarri, M, Adriani, O, Aguilar-Benitez, M, Ahlen, S, Alcaraz, J, Alemanni, G, Allaby, J, Aloisio, A, Alverson, G, Alviggi, M.G, Ambrosi, G, Anderhub, H, Andreev, V.P, Angelescu, T, Anselmo, F, Arefiev, A, Azemoon, T, Aziz, T, Bagnaia, P, Baksay, L, Banerjee, S, Banerjee, Sw, Banicz, K, Barczyk, A, Barillère, R, Barone, L, Bartalini, P, Baschirotto, A, Basile, M, Battiston, R, Bay, A, Becattini, F, Becker, U, Behner, F, Berdugo, J, Berges, P, Bertucci, B, Betev, B.L, Bhattacharya, S, Biasini, M, Biland, A, Bilei, G.M, Blaising, J.J, Blyth, S.C, Bobbink, G.J, Bock, R, Böhm, A, Boldizsar, L, Borgia, B, Bourilkov, D, Bourquin, M, Braccini, S, Branson, J.G, Brigljevic, V, Brock, I.C, Buffini, A, Buijs, A, Burger, J.D, Burger, W.J, Busenitz, J, Button, A, Cai, X.D, Campanelli, M, Capell, M, Cara Romeo, G, Carlino, G, Cartacci, A.M, Casaus, J, Castellini, G, Cavallari, F, Cavallo, N, Cecchi, C, Cerrada, M, Cesaroni, F, Chamizo, M, Chang, Y.H, Chaturvedi, U.K, Chekanov, S.V, Chemarin, M, Chen, A, Chen, G, Chen, G.M, Chen, H.F, Chen, H.S, Chereau, X, Chiefari, G, Chien, C.Y, Cifarelli, L, Cindolo, F, Civinini, C, Clare, I, Clare, R, Cohn, H.O, Coignet, G, Colijn, A.P, Colino, N, Commichau, V, Costantini, S, Cotorobai, F, de la Cruz, B, Csilling, A, Dai, T.S, D'Alessandro, R, de Asmundis, R, Degré, A, Deiters, K, della Volpe, D, Denes, P, DeNotaristefani, F, DiBitonto, D, Diemoz, M, van Dierendonck, D, Di Lodovico, F, Dionisi, C, Dittmar, M, Dominguez, A, Doria, A, Dova, M.T, Duchesneau, D, Duinker, P, Duran, I, Dutta, S, Easo, S, Efremenko, Yu, El Mamouni, H, Engler, A, Eppling, F.J, Erné, F.C, Ernenwein, J.P, Extermann, P, Fabre, M, Faccini, R, Falciano, S, Favara, A, Fay, J, Fedin, O, Felcini, M, Fenyi, B, Ferguson, T, Ferroni, F, Fesefeldt, H, Fiandrini, E, Field, J.H, Filthaut, F, Fisher, P.H, Fisk, I, Forconi, G, Fredj, L, Freudenreich, K, Furetta, C, Galaktionov, Yu, Ganguli, S.N, Garcia-Abia, P, Gau, S.S, Gentile, S, Gheordanescu, N, Giagu, S, Goldfarb, S, Goldstein, J, Gong, Z.F, Gougas, A, Gratta, G, Gruenewald, M.W, Gupta, V.K, Gurtu, A, Gutay, L.J, Hartmann, B, Hasan, A, Hatzifotiadou, D, Hebbeker, T, Hervé, A, van Hoek, W.C, Hofer, H, Hong, S.J, Hoorani, H, Hou, S.R, Hu, G, Innocente, V, Jenkes, K, Jin, B.N, Jones, L.W, de Jong, P, Josa-Mutuberria, I, Kasser, A, Khan, R.A, Kamrad, D, Kamyshkov, Yu, Kapustinsky, J.S, Karyotakis, Y, Kaur, M, Kienzle-Focacci, M.N, Kim, D, Kim, D.H, Kim, J.K, Kim, S.C, Kim, Y.G, Kinnison, W.W, Kirkby, A, Kirkby, D, Kirkby, J, Kiss, D, Kittel, W, Klimentov, A, König, A.C, Kopp, A, Korolko, I, Koutsenko, V, Kraemer, R.W, Krenz, W, Kunin, A, Ladron de Guevara, P, Laktineh, I, Landi, G, Lapoint, C, Lassila-Perini, K, Laurikainen, P, Lebeau, M, Lebedev, A, Lebrun, P, Lecomte, P, Lecoq, P, Le Coultre, P, Lee, H.J, Le Goff, J.M, Leiste, R, Leonardi, E, Levtchenko, P, Li, C, Lin, C.H, Lin, W.T, Linde, F.L, Lista, L, Liu, Z.A, Lohmann, W, Longo, E, Lu, W, Lu, Y.S, Lübelsmeyer, K, Luci, C, Luckey, D, Luminari, L, Lustermann, W, Ma, W.G, Maity, M, Majumder, G, Malgeri, L, Malinin, A, Maña, C, Mangeol, D, Mangla, S, Marchesini, P, Marin, A, Martin, J.P, Marzano, F, Massaro, G.G.G, McNally, D, McNeil, R.R, Mele, S, Merola, L, Meschini, M, Metzger, W.J, von der Mey, M, Mi, Y, Mihul, A, van Mil, A.J.W, Milcent, H, Mirabelli, G, Mnich, J, Molnar, P, Monteleoni, B, Moore, R, Morganti, S, Moulik, T, Mount, R, Müller, S, Muheim, F, Muijs, A.J.M, Nahn, S, Napolitano, M, Nessi-Tedaldi, F, Newman, H, Niessen, T, Nippe, A, Nisati, A, Nowak, H, Oh, Y.D, Opitz, H, Organtini, G, Ostonen, R, Palomares, C, Pandoulas, D, Paoletti, S, Paolucci, P, Park, H.K, Park, I.H, Pascale, G, Passaleva, G, Patricelli, S, Paul, T, Pauluzzi, M, Paus, C, Pauss, F, Peach, D, Pei, Y.J, Pensotti, S, Perret-Gallix, D, Petersen, B, Petrak, S, Pevsner, A, Piccolo, D, Pieri, M, Piroué, P.A, Pistolesi, E, Plyaskin, V, Pohl, M, Pojidaev, V, Postema, H, Produit, N, Prokofiev, D, Rahal-Callot, G, Raja, N, Rancoita, P.G, Rattaggi, M, Raven, G, Razis, P, Read, K, Ren, D, Rescigno, M, Reucroft, S, van Rhee, T, Riemann, S, Riles, K, Robohm, A, Rodin, J, Roe, B.P, Romero, L, Rosier-Lees, S, Rosselet, Ph, van Rossum, W, Roth, S, Rubio, J.A, Ruschmeier, D, Rykaczewski, H, Salicio, J, Sanchez, E, Sanders, M.P, Sarakinos, M.E, Sarkar, S, Sassowsky, M, Schäfer, C, Schegelsky, V, Schmidt-Kaerst, S, Schmitz, D, Schmitz, P, Scholz, N, Schopper, H, Schotanus, D.J, Schwenke, J, Schwering, G, Sciacca, C, Sciarrino, D, Servoli, L, Shevchenko, S, Shivarov, N, Shoutko, V, Shukla, J, Shumilov, E, Shvorob, A, Siedenburg, T, Son, D, Sopczak, A, Smith, B, Spillantini, P, Steuer, M, Stickland, D.P, Stone, A, Stone, H, Stoyanov, B, Straessner, A, Strauch, K, Sudhakar, K, Sultanov, G, Sun, L.Z, Susinno, G.F, Suter, H, Swain, J.D, Tang, X.W, Tauscher, L, Taylor, L, Ting, Samuel C.C, Ting, S.M, Tonutti, M, Tonwar, S.C, Tóth, J, Tully, C, Tuchscherer, H, Tung, K.L, Uchida, Y, Ulbricht, J, Uwer, U, Valente, E, Van de Walle, R.T, Vesztergombi, G, Vetlitsky, I, Viertel, G, Vivargent, M, Völkert, R, Vogel, H, Vogt, H, Vorobiev, I, Vorobyov, A.A, Vorvolakos, A, Wadhwa, M, Wallraff, W, Wang, J.C, Wang, X.L, Wang, Z.M, Weber, A, Wittgenstein, F, Wu, S.X, Wynhoff, S, Xu, J, Xu, Z.Z, Yang, B.Z, Yang, C.G, Yao, X.Y, Ye, J.B, Yeh, S.C, You, J.M, Zalite, An, Zalite, Yu, Zemp, P, Zeng, Y, Zhang, Z, Zhang, Z.P, Zhou, B, Zhu, G.Y, Zhu, R.Y, Zichichi, A, and Ziegler, F
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- 1998
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26. Class and Client in Beirut: The Sunni Muslim Community and the Lebanese State 1840-1985.
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Abukhalil, A. S.'Ad
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LEBANESE politics & government, 1946- ,NONFICTION - Abstract
The article reviews the book "Class and Client in Beirut: The Sunni Muslim Community and the Lebanese State 1840-1985," by Michael Johnson.
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- 1988
27. Advancement in biomedical implant materials-a mini review.
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S AD, P SPA, Naveen J, Khan T, and Khahro SH
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Metal alloys like stainless steel, titanium, and cobalt-chromium alloys are preferable for bio-implants due to their exceptional strength, tribological properties, and biocompatibility. However, long-term implantation of metal alloys can lead to inflammation, swelling, and itching because of ion leaching. To address this issue, polymers are increasingly being utilized in orthopedic applications, replacing metallic components such as bone fixation plates, screws, and scaffolds, as well as minimizing metal-on-metal contact in total hip and knee joint replacements. Ceramics, known for their hardness, thermal barrier, wear, and corrosion resistance, find extensive application in electrochemical, fuel, and biomedical industries. This review delves into a variety of biocompatible materials engineered to seamlessly integrate with the body, reducing adverse reactions like inflammation, toxicity, or immune responses. Additionally, this review examines the potential of various biomaterials including metals, polymers, and ceramics for implant applications. While metallic biomaterials remain indispensable, polymers and ceramics show promise as alternative options. However, surface-modified metallic materials offer a hybrid effect, combining the strengths of different constituents. The future of biomedical implant materials lies in advanced fabrication techniques and personalized designs, facilitating tailored solutions for complex medical needs., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 S., P., Naveen, Khan and Khahro.)
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- 2024
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28. Identification and characterization of a small molecule that activates thiosulfate sulfurtransferase and stimulates mitochondrial respiration.
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Al-Dahmani ZM, Hadian M, Ruiz-Moreno AJ, Maria SA, Batista FA, Zhang R, Luo Y, Sadremomtaz A, van der Straat R, Spoor M, Dolga AM, Dekker FJ, S S AD, van Goor H, and Groves MR
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- Mice, Humans, Animals, Molecular Docking Simulation, Kinetics, Mitochondria metabolism, Respiration, Obesity metabolism, Thiosulfate Sulfurtransferase chemistry, Thiosulfate Sulfurtransferase genetics, Thiosulfate Sulfurtransferase metabolism, Diabetes Mellitus metabolism
- Abstract
The enzyme Thiosulfate sulfurtransferase (TST, EC 2.8.1.1), is a positive genetic predictor of diabetes type 2 and obesity. As increased TST activity protects against the development of diabetic symptoms in mice, an activating compound for TST may provide therapeutic benefits in diabetes and obesity. We identified a small molecule activator of human TST through screening of an inhouse small molecule library. Kinetic studies in vitro suggest that two distinct isomers of the compound are required for full activation as well as an allosteric mode of activation. Additionally, we studied the effect of TST protein and the activator on TST activity through mitochondrial respiration. Molecular docking and molecular dynamics (MD) approaches supports an allosteric site for the binding of the activator, which is supported by the lack of activation in the Escherichia coli. mercaptopyruvate sulfurtransferase. Finally, we show that increasing TST activity in isolated mitochondria increases mitochondrial oxygen consumption., (© 2023 The Authors. Protein Science published by Wiley Periodicals LLC on behalf of The Protein Society.)
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- 2023
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29. Dietary self-management practices among persons with T2DM: An exploratory qualitative study from western-coast of India.
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Matpady P, Maiya AG, Saraswat PP, Mayya SS, Pai MS, S AD, and Umakanth S
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- Adult, Aged, Diabetes Mellitus, Type 2 psychology, Female, Follow-Up Studies, Humans, Male, Middle Aged, Prognosis, Qualitative Research, Social Support, Diabetes Mellitus, Type 2 diet therapy, Exercise, Health Behavior, Health Knowledge, Attitudes, Practice, Self-Management
- Abstract
Background: Diabetes is a significant public health challenge for India. Self-management, including dietary management, physical activity, stress management, and adherence to medication, is critical in glycaemic control. Though data concerning self-management, in general, are available among persons with Type 2 Diabetes Mellitus (T2DM), exclusive research on dietary self-management was limited., Aims: A qualitative study to explore the knowledge, current dietary practices, and the barriers and enablers for dietary self-care management in persons with T2DM., Methods: In this qualitative study, in-depth interviews were conducted among 35 participants with T2DM who scored minimally and optimally in the Diabetes Self-Management Questionnaire (DSMQ). Interviews were conducted using a validated interview guide. In-depth interviews were audio-recorded, transcribed to verbatim and thematically analysed., Results: The study included 20 males and 15 females. The three major themes derived in the study. Firstly, "Knowledge, Interpretation and Information" the majority of the participants have understood the influence of diet on control of blood glucose level includes food choices and quantum of food. Secondly, "Current Dietary Practices-Preferences, Availability of food and Convenience influence dietary practices': All participants had their own belief on the side effects and benefits of certain food items. Most of the participants followed a three-meal pattern: breakfast, lunch and dinner. Finally, Barriers and Enablers in dietary self-management practice. Knowledge, physical and emotional factors, behaviour, planning were the intrinsic factors. Elements of the research, social support, season and climate, food environment were the extrinsic factors and communication, and financial management was the intermediate influences observed., Conclusion: The themes generated by this research provide insight into self-management and patient expectations in dietary matters. It would be desirable for physicians and health care providers to be aware of these practices when advising people with T2DM on dietary self - management., Competing Interests: Declaration of competing interest The authors declare no conflict of interest., (Copyright © 2020 Diabetes India. Published by Elsevier Ltd. All rights reserved.)
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- 2020
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30. COVID-19 Special Column: COVID-19 Hits Native Hawaiian and Pacific Islander Communities the Hardest.
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Kaholokula JK, Samoa RA, Miyamoto RES, Palafox N, and Daniels SA
- Subjects
- COVID-19, Hawaii, Humans, Native Hawaiian or Other Pacific Islander, Residence Characteristics, Resilience, Psychological, SARS-CoV-2, Betacoronavirus, Coronavirus Infections economics, Coronavirus Infections epidemiology, Pandemics economics, Pneumonia, Viral economics, Pneumonia, Viral epidemiology
- Published
- 2020
31. Protective effect of Abutilon indicum against lead-induced reproductive toxicity in male Wistar rats.
- Author
-
R S and S AD
- Abstract
Despite ample literature on the toxic impact of lead on the environment and health, the exact mechanism of pathogenesis/toxicity is not clearly known. Because it is well established that lead induces oxidative stress, it is assumed that exposure to antioxidants may reduce the toxic impact of lead. In this study, we evaluated the impact of coadministration of the methanolic root extract of a plant Abutilon indicum (50, 100, 200 mg kg
-1 b.wt.) in mitigating the toxic impact of lead on the reproductive system of rats. In brief, Wistar rats were exposed to lead acetate in drinking water with or without coadministration of plant root extract and compared with that of control animals. After 45 days of exposure as outlined above, the animals were killed and the reproductive toxicity was assessed by sperm parameters, hormone and antioxidant enzyme assays, and testis histopathology. Significant reduction in testis weight, sperm count, testosterone levels, and antioxidant enzymes levels such as Superoxide Dismutase, Catalase, and Glutathione peroxidase was seen in lead-treated animals, confirming the toxic impact. The coadministration of A. Indicum (100 and 200 mg kg-1 b.wt.) was found to bring the studied parameters close to the levels seen in untreated (control) animals. Our findings are indicative of the protective nature of A. Indicum against lead-induced reproductive toxicity in a dose-dependent manner. However, further characterization of the root extract is required to elucidate the probable mechanism of protection., (© 2019 Wiley Periodicals, Inc.)- Published
- 2019
- Full Text
- View/download PDF
32. Mobilization of Hematopoietic Progenitor Cells for Autologous Transplantation Using Pegfilgrastim and Plerixafor: Efficacy and Cost Implications.
- Author
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Watts NL, Marques MB, Peavey DB, Innis-Shelton R, Saad A, Ad S, Salzman D, Lamb LS Jr, and Costa LJ
- Subjects
- Adult, Aged, Female, Humans, Male, Middle Aged, Transplantation, Autologous, Costs and Cost Analysis, Filgrastim administration & dosage, Filgrastim economics, Hematopoietic Stem Cell Mobilization economics, Lymphoma economics, Lymphoma pathology, Lymphoma therapy, Peripheral Blood Stem Cell Transplantation economics, Polyethylene Glycols administration & dosage, Polyethylene Glycols economics
- Abstract
Filgrastim (FIL) is the most common growth factor combined with plerixafor for autologous hematopoietic progenitor cell mobilization, but requires daily, multi-injection administration. We adopted a standardized mobilization regimen with pegfilgrastim (PEG) and upfront plerixafor, allowing for a single injection given the long half-life and slow elimination of PEG. Between 2015 and 2017, a total of 235 patients with lymphoma or plasma cell dyscrasias underwent mobilization with PEG 6 mg on day 1 and upfront plerixafor 24 mg on day 3, followed by apheresis on day 4 regardless of peripheral blood CD34
+ cells. The median CD34+ cells/mm3 in peripheral blood on first day of collection was 48 and median collection yield was 7.27 × 106 CD34+ cells/kg (range, 0.32 to 39.6 × 106 CD34+ cells/kg) after a mean of 1.6 apheresis collections. Overall, 83% of patients achieved the mobilization target, and 95% reached the minimum necessary CD34+ cell yield to proceed with transplantation (2 × 106 CD34+ cells/kg). Because FIL is weight-based and dosed daily, the cost comparison with PEG is influenced by patient weight and number of apheresis sessions required. A cost simulation using actual patient data indicates that PEG is associated with lower cost than FIL for the majority of patients. Autologous hematopoietic progenitor cell mobilization with PEG and plerixafor is practical, effective, and not associated with increased cost compared with FIL mobilization., (Copyright © 2018. Published by Elsevier Inc.)- Published
- 2019
- Full Text
- View/download PDF
33. Blue emitting copper nanoclusters as colorimetric and fluorescent probe for the selective detection of bilirubin.
- Author
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R S A, J S AD, John N, K A, S S S, and George S
- Subjects
- Color, Fluorescence, Humans, Limit of Detection, Bilirubin urine, Colorimetry methods, Copper chemistry, Fluorescent Dyes chemistry, Metal Nanoparticles chemistry, Spectrometry, Fluorescence methods
- Abstract
Hurdles to develop point of care diagnostic methods restrict the translation of progress in the health care sector from bench side to bedside. In this article a simple, cost effective fluorescent as well as colorimetric nanosensor was developed for the early and easy detection of hyperbilirubinemia. A stable, water soluble bovine serum albumin stabilised copper nanocluster (BSA CuNC) was used as the fluorescent probe which exhibited strong blue emission (404nm) upon 330nm excitation. The fluorescence of the BSA CuNC can be effectively quenched by the addition of bilirubin by the formation of copper-bilirubin complex. Meanwhile the copper-bilirubin complex resulted in an observable colour change from pale violet to green facilitating colorimetric detection. The prepared sensor displayed good selectivity and sensitivity over other co-existing molecules, and can be used for quantifying bilirubin with a detection limit down to 257fM. Additionally, the as-prepared probe was coated on a paper strip to develop a portable paper strip sensor of bilirubin. Moreover, the method was successfully applied in real sample analysis and obtained promising result., (Copyright © 2018 Elsevier B.V. All rights reserved.)
- Published
- 2018
- Full Text
- View/download PDF
34. ATP-driven and AMPK-independent autophagy in an early branching eukaryotic parasite.
- Author
-
Li FJ, Xu ZS, Soo AD, Lun ZR, and He CY
- Subjects
- Amino Acids deficiency, Animals, Autophagosomes drug effects, Autophagosomes metabolism, Energy Metabolism drug effects, Glucose metabolism, Life Cycle Stages, Parasites drug effects, Proline metabolism, Trypanosoma brucei brucei drug effects, Trypanosoma brucei brucei growth & development, AMP-Activated Protein Kinases metabolism, Adenosine Triphosphate pharmacology, Autophagy drug effects, Parasites cytology, Parasites enzymology, Trypanosoma brucei brucei cytology, Trypanosoma brucei brucei enzymology
- Abstract
Autophagy is a catabolic cellular process required to maintain protein synthesis, energy production and other essential activities in starved cells. While the exact nutrient sensor(s) is yet to be identified, deprivation of amino acids, glucose, growth factor and other nutrients can serve as metabolic stimuli to initiate autophagy in higher eukaryotes. In the early-branching unicellular parasite Trypanosoma brucei, which can proliferate as procyclic form (PCF) in the tsetse fly or as bloodstream form (BSF) in animal hosts, autophagy is robustly triggered by amino acid deficiency but not by glucose depletion. Taking advantage of the clearly defined adenosine triphosphate (ATP) production pathways in T. brucei, we have shown that autophagic activity depends on the levels of cellular ATP production, using either glucose or proline as a carbon source. While autophagosome formation positively correlates with cellular ATP levels; perturbation of ATP production by removing carbon sources or genetic silencing of enzymes involved in ATP generation pathways, also inhibited autophagy. This obligate energy dependence and the lack of glucose starvation-induced autophagy in T. brucei may reflect an adaptation to its specialized, parasitic life style.
- Published
- 2017
- Full Text
- View/download PDF
35. Effects of crude extracts of a saxitoxin-producer strain of the cyanobacterium Cylindrospermopsis raciborskii on the swimming behavior of wild and laboratory reared guppy Poecilia vivipara.
- Author
-
Lopes KC, Ferrão-Filho AD, Dos Santos EG, Cunha RA, and Santos CP
- Subjects
- Alkaloids, Animals, Bacterial Toxins toxicity, Cyanobacteria Toxins, Enzyme-Linked Immunosorbent Assay, Uracil analogs & derivatives, Uracil toxicity, Behavior, Animal drug effects, Cylindrospermopsis chemistry, Poecilia, Saxitoxin toxicity, Swimming
- Abstract
The cyanobacterium Cylindrospermopsis raciborskii is an invasive species in water supply reservoirs worldwide, which can produces cylindrospermopsins and saxitoxins. In the wild, guppy (Poecilia vivipara) can be exposed to cyanotoxins, but those born and reared in laboratory are free of this contact. The aim of this paper was to comparatively measure the locomotor activity of 'wild' and 'lab' P. vivipara before and after exposure to crude extracts of two different cultures of C. raciborskii (CYRF-01), a saxitoxin-procucer strain. The movement of each fish was recorded using an image monitoring system (Videomex V
® ) before and after 48 h exposure to cyanobacterial extracts. Each experiment was performed during 4 h, with 1 h acclimation and 3 h recording period of the parameters Distance performed (DP), Swimming time (SwT), Stereotypic time (StT), Resting time (RT) and Average speed (AS). The quantification of saxitoxin in the solutions was performed by the enzyme-linked immunosorbent assay (ELISA). The weight or the total length did not influence the locomotor activity of fish in any of the experiments. The saxitoxin value was similar for both cultures (Culture 1: 7.3 μg L-1 and Culture 2: 8.6 μg L-1 ). However, in experiments with Culture 1 an increased activity in most parameters was observed, while in Culture 2, a decreased activity was observed only in 'lab' fish. Wild fish was less affected, showing higher resistance to both cyanobacterial crude extracts. This study showed that different cultures of the same strain of C. raciborskii and with similar contents of saxitoxin are able to change the locomotor activity of P. vivipara, contributing to the validation of the use of behavioral parameters to the evaluation of sublethal effects of toxic cyanobacteria on fish., (Copyright © 2017 Elsevier Ltd. All rights reserved.)- Published
- 2017
- Full Text
- View/download PDF
36. The yielding transition in amorphous solids under oscillatory shear deformation.
- Author
-
Leishangthem P, Parmar AD, and Sastry S
- Abstract
Amorphous solids are ubiquitous among natural and man-made materials. Often used as structural materials for their attractive mechanical properties, their utility depends critically on their response to applied stresses. Processes underlying such mechanical response, and in particular the yielding behaviour of amorphous solids, are not satisfactorily understood. Although studied extensively, observed yielding behaviour can be gradual and depend significantly on conditions of study, making it difficult to convincingly validate existing theoretical descriptions of a sharp yielding transition. Here we employ oscillatory deformation as a reliable probe of the yielding transition. Through extensive computer simulations for a wide range of system sizes, we demonstrate that cyclically deformed model glasses exhibit a sharply defined yielding transition with characteristics that are independent of preparation history. In contrast to prevailing expectations, the statistics of avalanches reveals no signature of the impending transition, but exhibit dramatic, qualitative, changes in character across the transition.
- Published
- 2017
- Full Text
- View/download PDF
37. Essential Oil of Aristolochia trilobata: Synthesis, Routes of Exposure, Acute Toxicity, Binary Mixtures and Behavioral Effects on Leaf-Cutting Ants.
- Author
-
de Oliveira BM, Melo CR, Alves PB, Santos AA, Santos AC, Santana AD, Araújo AP, Nascimento PE, Blank AF, and Bacci L
- Subjects
- Animals, Ants physiology, Behavior, Animal drug effects, Chromatography, Gas, Fumigation, Insecticides pharmacology, Oils, Volatile pharmacology, Plant Leaves chemistry, Plant Oils chemistry, Plant Oils pharmacology, Ants drug effects, Aristolochia chemistry, Insecticides chemistry, Oils, Volatile chemistry
- Abstract
Plants of the genus Aristolochia have been frequently reported as important medicinal plants. Despite their high bioactive potential, to date, there are no reports of their effects on leaf-cutting ants. Therefore, the present study aimed to evaluate the insecticidal activity of the essential oil of Aristolochia trilobata and its major components on Atta sexdens and Acromyrmex balzani , two species of leaf-cutting ants. The bioassays were performed regarding routes of exposure, acute toxicity, binary mixtures of the major components and behavioral effects. Twenty-five components were identified in the essential oil of A. trilobata using a gas chromatographic system equipped with a mass spectrometer and a flame ionization detector. The components found in higher proportions were sulcatyl acetate, limonene, p -cymene and linalool. The essential oil of A. trilobata and its individual major components were efficient against A. balzani and A. sexdens workers when applied by fumigation. These components showed fast and efficient insecticidal activity on ants. The components acted synergistically and additively on A. balzani and A. sexdens , respectively, and caused a strong repellency/irritability in the ants. Thus, our results demonstrate the great potential of the essential oil of A. trilobata and its major components for the development of new insecticides.
- Published
- 2017
- Full Text
- View/download PDF
38. Emergence of mmpT5 Variants during Bedaquiline Treatment of Mycobacterium intracellulare Lung Disease.
- Author
-
Alexander DC, Vasireddy R, Vasireddy S, Philley JV, Brown-Elliott BA, Perry BJ, Griffith DE, Benwill JL, Cameron AD, and Wallace RJ Jr
- Subjects
- Aged, Female, Genome, Bacterial, Humans, Male, Microbial Sensitivity Tests, Middle Aged, Mycobacterium avium Complex isolation & purification, Recurrence, Sequence Analysis, DNA, Tuberculosis, Pulmonary microbiology, Antitubercular Agents therapeutic use, Diarylquinolines therapeutic use, Drug Resistance, Bacterial, Mutation, Missense, Mycobacterium avium Complex genetics, Transcription Factors genetics, Tuberculosis, Pulmonary drug therapy
- Abstract
Bedaquiline (BDQ), a diarylquinoline antibiotic that targets ATP synthase, is effective for the treatment of Mycobacterium tuberculosis infections that no longer respond to conventional drugs. While investigating the off-label use of BDQ as salvage therapy, seven of 13 patients with Mycobacterium intracellulare lung disease had an initial microbiological response and then relapsed. Whole-genome comparison of pretreatment and relapse isolates of M. intracellulare uncovered mutations in a previously uncharacterized locus, mmpT5 Preliminary analysis suggested similarities between mmpT5 and the mmpR5 locus, which is associated with low-level BDQ resistance in M. tuberculosis Both genes encode transcriptional regulators and are adjacent to orthologs of the mmpS5-mmpL5 drug efflux operon. However, MmpT5 belongs to the TetR superfamily, whereas MmpR5 is a MarR family protein. Targeted sequencing uncovered nonsynonymous mmpT5 mutations in isolates from all seven relapse cases, including two pretreatment isolates. In contrast, only two relapse patient isolates had nonsynonymous changes in ATP synthase subunit c (atpE), the primary target of BDQ. Susceptibility testing indicated that mmpT5 mutations are associated with modest 2- to 8-fold increases in MICs for BDQ and clofazimine, whereas one atpE mutant exhibited a 50-fold increase in MIC for BDQ. Bedaquiline shows potential for the treatment of M. intracellulare lung disease, but optimization of treatment regimens is required to prevent the emergence of mmpT5 variants and microbiological relapse., (Copyright © 2017 American Society for Microbiology.)
- Published
- 2017
- Full Text
- View/download PDF
39. Whole-Genome Sequence and Annotation of Salmonella enterica subsp. enterica Serovar Enteritidis Phage Type 8 Strain EN1660.
- Author
-
Perry BJ, Fitzgerald SF, Kröger C, and Cameron AD
- Abstract
The genome of Salmonella enterica subspecies enterica serovar Enteritidis phage type 8 strain EN1660, isolated from an outbreak in Thunder Bay, Canada, was sequenced to 46-fold coverage using an Illumina MiSeq with 300-bp paired-end sequencing chemistry to produce 28 contigs with an N
50 value of 490,721 bp., (Copyright © 2017 Perry et al.)- Published
- 2017
- Full Text
- View/download PDF
40. A circuitry for sleep in Parkinson´s disease.
- Author
-
Targa AD and Lima MM
- Published
- 2017
- Full Text
- View/download PDF
41. Initial development and preliminary evaluation of a multiplex bead assay to detect antibodies to Ehrlichia canis, Anaplasma platys, and Ehrlichia chaffeensis outer membrane peptides in naturally infected dogs from Grenada, West Indies.
- Author
-
Wilkerson MJ, Black KE, Lanza-Perea M, Sharma B, Gibson K, Stone DM, George A, Nair AD, and Ganta RR
- Subjects
- Anaplasma immunology, Anaplasma isolation & purification, Animals, Antibodies, Bacterial blood, Dog Diseases blood, Dog Diseases microbiology, Dogs, Ehrlichia canis immunology, Ehrlichia canis isolation & purification, Ehrlichia chaffeensis immunology, Ehrlichia chaffeensis isolation & purification, Ehrlichiosis diagnosis, Enzyme-Linked Immunosorbent Assay veterinary, Grenada, Predictive Value of Tests, Dog Diseases diagnosis, Ehrlichiosis veterinary
- Abstract
Tick-borne bacteria, Ehrlichia canis, Anaplasma platys, and Ehrlichia chaffeensis are significant pathogens of dogs worldwide, and coinfections of E. canis and A. platys are common in dogs on the Caribbean islands. We developed and evaluated the performance of a multiplex bead-based assay to detect antibodies to E. canis, A. platys, and E. chaffeensis peptides in dogs from Grenada, West Indies, where E. canis and A. platys infections are endemic. Peptides from outer membrane proteins of P30 of E. canis, OMP-1X of A. platys, and P28-19/P28-14 of E. chaffeensis were coupled to magnetic beads. The multiplex peptide assay detected antibodies in dogs experimentally infected with E. canis and E. chaffeensis, but not in an A. platys experimentally infected dog. In contrast, the multiplex assay and an in-house enzyme-linked immunosorbent assay (ELISA) detected A. platys antibodies in naturally infected Grenadian dogs. Following testing of 104 Grenadian canine samples, multiplex assay results had good agreement with commercially available ELISA and immunofluorescent assay for E. canis antibody-positive dogs ( K values of 0.73 and 0.84), whereas A. platys multiplex results had poor agreement with these commercial assays ( K values of -0.02 and 0.01). Prevalence of seropositive E. canis and A. platys Grenadian dogs detected by the multiplex and commercial antibody assays were similar to previous reports. Although the multiplex peptide assay performed well in detecting the seropositive status of dogs to E. canis and had good agreement with commercial assays, better antigen targets are necessary for the antibody detection of A. platys.
- Published
- 2017
- Full Text
- View/download PDF
42. Genetic Regulation of Virulence and Antibiotic Resistance in Acinetobacter baumannii.
- Author
-
Kröger C, Kary SC, Schauer K, and Cameron AD
- Abstract
Multidrug resistant microorganisms are forecast to become the single biggest challenge to medical care in the 21st century. Over the last decades, members of the genus Acinetobacter have emerged as bacterial opportunistic pathogens, in particular as challenging nosocomial pathogens because of the rapid evolution of antimicrobial resistances. Although we lack fundamental biological insight into virulence mechanisms, an increasing number of researchers are working to identify virulence factors and to study antibiotic resistance. Here, we review current knowledge regarding the regulation of virulence genes and antibiotic resistance in Acinetobacter baumannii . A survey of the two-component systems AdeRS, BaeSR, GacSA and PmrAB explains how each contributes to antibiotic resistance and virulence gene expression, while BfmRS regulates cell envelope structures important for pathogen persistence. A. baumannii uses the transcription factors Fur and Zur to sense iron or zinc depletion and upregulate genes for metal scavenging as a critical survival tool in an animal host. Quorum sensing, nucleoid-associated proteins, and non-classical transcription factors such as AtfA and small regulatory RNAs are discussed in the context of virulence and antibiotic resistance., Competing Interests: The authors declare no conflict of interest. The funding sponsors had no role in the writing of the manuscript.
- Published
- 2016
- Full Text
- View/download PDF
43. Structure-behavior study of a family of "hybrid cyanine" dyes which exhibit inverted solvatochromism.
- Author
-
Stock RI, de Melo CE, Schramm AD, Nicoleti CR, Bortoluzzi AJ, Heying RD, Machado VG, and Rezende MC
- Abstract
The inverted solvatochromism of twenty dyes containing an electron-donor phenolate conjugated with an electron-withdrawing nitro-substituted phenyl ring was analyzed in terms of the dye structure and substituents. Structural factors that increased the difference between the electrophilicities of the donor and acceptor moieties, or the donor-acceptor strength of the phenolate dyes, also increased the sensitivity of the dyes to solvent-polarity changes and red-shifted their solvatochromic absorption bands.
- Published
- 2016
- Full Text
- View/download PDF
44. Unraveling a new circuitry for sleep regulation in Parkinson's disease.
- Author
-
Targa AD, Rodrigues LS, Noseda AC, Aurich MF, Andersen ML, Tufik S, da Cunha C, and Lima MM
- Subjects
- 3,4-Dihydroxyphenylacetic Acid metabolism, Animals, Corpus Striatum drug effects, Dopamine Agonists pharmacology, Dopamine D2 Receptor Antagonists pharmacology, Male, Methoxyhydroxyphenylglycol analogs & derivatives, Methoxyhydroxyphenylglycol metabolism, Nerve Net drug effects, Pars Compacta drug effects, Rats, Rats, Wistar, Sleep Stages drug effects, Corpus Striatum metabolism, Nerve Net metabolism, Parkinson Disease metabolism, Pars Compacta metabolism, Sleep Stages physiology
- Abstract
Sleep disturbances are among the most disabling non-motor symptoms in Parkinson's disease. The pedunculopontine tegmental nucleus and basal ganglia are likely involved in these dysfunctions, as they are affected by neurodegeneration in Parkinson's disease and have a role in sleep regulation. To investigate this, we promoted a lesion in the pedunculopontine tegmental nucleus or substantia nigra pars compacta of male rats, followed by 24 h of REM sleep deprivation. Then, we administrated a dopaminergic D2 receptor agonist, antagonist or vehicle directly in the striatum. After a period of 24 h of sleep-wake recording, we observed that the ibotenic acid infusion in the pedunculopontine tegmental nucleus blocked the so-called sleep rebound effect mediated by REM sleep deprivation, which was reversed by striatal D2 receptors activation. Rotenone infusion in the substantia nigra pars compacta also blocked the sleep rebound, however, striatal D2 receptors activation did not reverse it. In addition, rotenone administration decreased the time spent in NREM sleep, which was corroborated by positive correlations between dopamine levels in both substantia nigra pars compacta and striatum and the time spent in NREM sleep. These findings suggest a new circuitry for sleep regulation in Parkinson's disease, involving the triad composed by pedunculopontine nucleus, substantia nigra pars compacta and striatum, evidencing a potential therapeutic target for the sleep disturbances associated to this pathology., (Copyright © 2016 Elsevier Ltd. All rights reserved.)
- Published
- 2016
- Full Text
- View/download PDF
45. Reverse solvatochromism in solvent binary mixtures: a case study using a 4-(nitrostyryl)phenolate as a probe.
- Author
-
Stock RI, Schramm AD, Rezende MC, and Machado VG
- Abstract
A 4-(nitrostyryl)phenolate was synthesized and its use in pure solvents revealed a reversion in solvatochromism. Solutions of a dye in binary solvent mixtures, using as components the solvents in the region of the occurrence of the reversion, provided the first case in the literature of reverse solvatochromism in a binary mixture.
- Published
- 2016
- Full Text
- View/download PDF
46. Drying kinetics and mathematical modeling of hot air drying of coconut coir pith.
- Author
-
Fernando JA and Amarasinghe AD
- Abstract
Drying kinetics of coir pith was studied and the properties of compressed coir pith discs were analyzed. Coir pith particles were oven dried in the range of temperatures from 100 to 240 °C and the rehydration ability of compressed coir pith was evaluated by finding the volume expansion. The optimum drying temperature was found to be 140 °C. Hot air drying was carried out to examine the drying kinetics by allowing the coir pith particles to fluidize and circulate inside the drying chamber. Particle motion within the drying chamber closely resembled the particle motion in a flash dryer. The effective moisture diffusivity was found to increase from 1.18 × 10(-8) to 1.37 × 10(-8) m(2)/s with the increase of air velocity from 1.4 to 2.5 m/s respectively. Correlation analysis and residual plots were used to determine the adequacy of existing mathematical models for describing the drying behavior of coir pith. The empirical models, Wang and Singh model and Linear model, were found to be adequate for accurate prediction of drying behavior of coir pith. A new model was proposed by modifying the Wang and Singh model and considering the effect of air velocity. It gave the best correlation between observed and predicted moisture ratio with high value of coefficient of determination (R(2)) and lower values of root mean square error, reduced Chi square (χ(2)) and mean relative deviation (E%).
- Published
- 2016
- Full Text
- View/download PDF
47. A Specific Angiographic View of Left Coronary Artery Bifurcation in the Left Main Percutaneous Coronary Intervention Era.
- Author
-
Reis SS, Botelho RV, Abizaid A, Pereira AD, Alves R, de Souza DF, and Ferreira-Filho SR
- Subjects
- Aged, Female, Humans, Male, Middle Aged, Observer Variation, Reproducibility of Results, Coronary Angiography methods, Coronary Vessels diagnostic imaging, Percutaneous Coronary Intervention methods
- Abstract
Objectives: We propose a right lateral (90-120° RAO) with 30° cranial angiographic view to expose the bifurcation of the left main coronary artery (LMCA) when previously used routine projections were inefficient at clearly showing this region., Background: Little has been published in the medical literature regarding angiographic projections dedicated to special anatomies., Methods: A total of 84 patients were subjected to the proposed projections. A reproducibility study, conducted with the participation of 2 independent observers, judged the effectiveness of the proposed projection. The Prevalence and Bias Adjusted Kappa (PABAK) index, with a 95% confidence interval (CI), was used to demonstrate the intensity of intra/inter-observer agreement., Results: The proposed projection was efficient in 79% of the angiograms, with agreement of 0.76 (0.6-0.9; P ≤ 0.001). The origins and the proximal segments of: the anterior descending coronary artery were exposed in 89% of the angiograms, agreement of 0.86 (0.7-1.0; P ≤ 0.001); the circumflex artery were exposed in 83% of the angiograms, with agreement of 0.72 (0.5-1.0; P ≤ 0.001); and the intermediate branch, when present, were exposed in 89% of the angiograms, agreement of 0.79 (0.6-1.0; P ≤ 0.001)., Conclusion: The right lateral (90-120° RAO) with 30° cranial projection is effective, safe, and reproducible. In special situations where routine projections fail, this proposed projection can reveal important details of the anatomy of the bifurcation of the LMCA during conventional coronary angiography or be the working projection during coronary angioplasty. (J Interven Cardiol 2016;29:293-299)., (© 2016, Wiley Periodicals, Inc.)
- Published
- 2016
- Full Text
- View/download PDF
48. A New Dicynodont (Therapsida: Anomodontia) from the Permian of Southern Brazil and Its Implications for Bidentalian Origins.
- Author
-
Boos AD, Kammerer CF, Schultz CL, Soares MB, and Ilha AL
- Subjects
- Animals, Brazil, Biological Evolution, Fossils, Mammals anatomy & histology, Mammals classification
- Abstract
Dicynodonts were a highly successful group of herbivorous therapsids that inhabited terrestrial ecosystems from the Middle Permian through the end of the Triassic periods. Permian dicynodonts are extremely abundant in African deposits, but are comparatively poorly known from the other regions of Gondwana. Here we describe a new South American dicynodont, Rastodon procurvidens gen. et sp. nov., from the Boqueirão farm site of the Rio do Rasto Formation, Paraná Basin, Guadalupian/Lopingian of Brazil. Diagnostic features of R. procurvidens include uniquely anteriorly-curved maxillary tusks, well-developed ridges extending from the crista oesophagea anteriorly along the pterygoid rami, strong posterior angulation of the posterior pterygoid rami, and a bulbous, well-developed retroarticular process of the articular. Phylogenetic analysis indicates that R. procurvidens is the earliest and most basal member of Bidentalia, a cosmopolitan clade that includes Permian and Triassic dicynodonts whose dentition is usually reduced to a pair of maxillary tusks.
- Published
- 2016
- Full Text
- View/download PDF
49. Study on small molecular organic compounds pyrolysed from rubber seed oil and its sodium soap.
- Author
-
Fernando TL, Prashantha MA, and Amarasinghe AD
- Abstract
Rubber seed oil (RSO) and its sodium soap were pyrolysed in a batch reactor to obtain low molar mass organic substances. The pyrolitic oil of RSO was redistilled and the distillates were characterized by GC-MS and FTIR. Density, acid value, saponification value and ester values were also measured according to the ASTM standard methods. A similar analysis was done for samples taken out at different time intervals from the reaction mixture. Industrially important low molar mass alkanes, alkenes, aromatics, cyclic compounds and carboxylic acids were identified in the pyrolysis process of rubber seed oil. However, pyrolysis of the sodium soap of rubber seed oil gave a mixture of hydrocarbons in the range of C14-C17 and hence it has more applications as a fuel.
- Published
- 2016
- Full Text
- View/download PDF
50. Lactobacillus reuteri Inhibition of Enteropathogenic Escherichia coli Adherence to Human Intestinal Epithelium.
- Author
-
Walsham AD, MacKenzie DA, Cook V, Wemyss-Holden S, Hews CL, Juge N, and Schüller S
- Abstract
Enteropathogenic Escherichia coli (EPEC) is a major cause of diarrheal infant death in developing countries, and probiotic bacteria have been shown to provide health benefits in gastrointestinal infections. In this study, we have investigated the influence of the gut symbiont Lactobacillus reuteri on EPEC adherence to the human intestinal epithelium. Different host cell model systems including non-mucus-producing HT-29 and mucus-producing LS174T intestinal epithelial cell lines as well as human small intestinal biopsies were used. Adherence of L. reuteri to HT-29 cells was strain-specific, and the mucus-binding proteins CmbA and MUB increased binding to both HT-29 and LS174T cells. L. reuteri ATCC PTA 6475 and ATCC 53608 significantly inhibited EPEC binding to HT-29 but not LS174T cells. While pre-incubation of LS174T cells with ATCC PTA 6475 did not affect EPEC attaching/effacing (A/E) lesion formation, it increased the size of EPEC microcolonies. ATCC PTA 6475 and ATCC 53608 binding to the mucus layer resulted in decreased EPEC adherence to small intestinal biopsy epithelium. Our findings show that L. reuteri reduction of EPEC adhesion is strain-specific and has the potential to target either the epithelium or the mucus layer, providing further rationale for the selection of probiotic strains.
- Published
- 2016
- Full Text
- View/download PDF
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