Author: "Saberi B" - Searchworks@Jio Institute Digital Library Search Results

428 results on '"Saberi B"'

1. Impact of Local Therapy on Outcomes in Patients with Recurrent Hepatocellular Carcinoma after Liver Transplantation

Author: Lin, T.A., primary, Paul, N., additional, Cheung, D., additional, Saberi, B., additional, Ottman, S., additional, Gurakar, A., additional, Yarchoan, M., additional, Narang, A., additional, Kim, A.K., additional, and Meyer, J.J., additional
Published: 2023
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2. The impact of peppermint oil on the irritable bowel syndrome: a meta-analysis of the pooled clinical data

Author: Alammar, N., Wang, L., Saberi, B., Nanavati, J., Holtmann, G., Shinohara, R. T., and Mullin, G. E.
Published: 2019
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3. Fehlbildungen

Author: Riede, U.N., Brand-Saberi, B., Riede, Ursus-Nikolaus, Werner, Martin, and Freudenberg, Nikolaus
Published: 2009
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4. Ätiologie und Pathogenese der Arthrofibrose auf zellulärer Ebene: Was ist für den Kliniker relevant?

Author: Krenn, V., Haj, A. A., Gehrke, T., Kendoff, D., Perino, G., Brand-Saberi, B., Faust, I., and Traut, P.
Published: 2016
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5. Emerging inflammatory bowel disease demographics, phenotype, and treatment in South Asia, South-East Asia, and Middle East: Preliminary findings from the Inflammatory Bowel Disease-Emerging Nations' Consortium

Author: Banerjee, R, Pal, P, Hilmi, I, Ghoshal, UC, Desai, DC, Rahman, MM, Dutta, U, Mohiuddin, SA, Al Mohannadi, M, Philip, M, Ramesh, GN, Niriella, MA, De Silva, AP, de Silva, HJ, Pisespongsa, P, Limsrivilai, J, Aniwan, S, Nawarathne, M, Fernandopulle, N, Aye, TT, Ni, N, Al Awadhi, S, Joshi, N, Ngoc, PTV, Kieu, TV, Nguyen, AD, Abdullah, M, Ali, E, Zeid, A, Sollano, JD, Saberi, B, Omar, M, Mohsin, MN, Aftab, H, Wai, TM, Shastri, YM, Chaudhuri, S, Ahmed, F, Bhatia, SJ, Travis, SPL, and group, Inflammatory Bowel Disease-Emerging Nations' Consortium (IBD-ENC) study
Subjects: Male, Delayed Diagnosis, Hepatology, Asia, Eastern, Incidence, Gastroenterology, Inflammatory Bowel Diseases, Cross-Sectional Studies, Phenotype, Crohn Disease, Humans, Immunologic Factors, Colitis, Ulcerative, Female, Mesalamine, Asia, Southeastern, Aged
Abstract: Background and Aim: Inflammatory bowel disease (IBD) is emerging in the newly industrialized countries of South Asia, South-East Asia, and the Middle East, yet epidemiological data are scarce. Methods: We performed a cross-sectional study of IBD demographics, disease phenotype, and treatment across 38 centers in 15 countries of South Asia, South-East Asia, and Middle East. Intergroup comparisons included gross national income (GNI) per capita. Results: Among 10 400 patients, ulcerative colitis (UC) was twice as common as Crohn's disease (CD), with a male predominance (UC 6678, CD 3495, IBD unclassified 227, and 58% male). Peak age of onset was in the third decade, with a low proportion of elderly-onset IBD (5% age > 60). Familial IBD was rare (5%). The extent of UC was predominantly distal (proctitis/left sided 67%), with most being treated with mesalamine (94%), steroids (54%), or immunomodulators (31%). Ileocolic CD (43%) was the commonest, with low rates of perianal disease (8%) and only 6% smokers. Diagnostic delay for CD was common (median 12 months; interquartile range 5–30). Treatment of CD included mesalamine, steroids, and immunomodulators (61%, 51%, and 56%, respectively), but a fifth received empirical antitubercular therapy. Treatment with biologics was uncommon (4% UC and 13% CD), which increased in countries with higher GNI per capita. Surgery rates were 0.1 (UC) and 2 (CD) per 100 patients per year. Conclusions: The IBD-ENC cohort provides insight into IBD in South-East Asia and the Middle East, but is not yet population based. UC is twice as common as CD, familial disease is uncommon, and rates of surgery are low. Biologic use correlates with per capita GNI.
Published: 2022

6. On the development of the human hand

Author: Christ, B., Jacob, H. J., Brand-Saberi, B., Grim, M., Preuschoft, Holger, editor, and Chivers, David J., editor
Published: 1993
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7. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Author: Klionsky, DJ, Abdel-Aziz, AK, Abdelfatah, S, Abdellatif, M, Abdoli, A, Abel, S, Abeliovich, H, Abildgaard, MH, Abudu, YP, Acevedo-Arozena, A, Adamopoulos, IE, Adeli, K, Adolph, TE, Adornetto, A, Aflaki, E, Agam, G, Agarwal, A, Aggarwal, BB, Agnello, M, Agostinis, P, Agrewala, JN, Agrotis, A, Aguilar, PV, Ahmad, ST, Ahmed, ZM, Ahumada-Castro, U, Aits, S, Aizawa, S, Akkoc, Y, Akoumianaki, T, Akpinar, HA, Al-Abd, AM, Al-Akra, L, Al-Gharaibeh, A, Alaoui-Jamali, MA, Alberti, S, Alcocer-Gómez, E, Alessandri, C, Ali, M, Alim Al-Bari, MA, Aliwaini, S, Alizadeh, J, Almacellas, E, Almasan, A, Alonso, A, Alonso, GD, Altan-Bonnet, N, Altieri, DC, Álvarez, ÉMC, Alves, S, Alves da Costa, C, Alzaharna, MM, Amadio, M, Amantini, C, Amaral, C, Ambrosio, S, Amer, AO, Ammanathan, V, An, Z, Andersen, SU, Andrabi, SA, Andrade-Silva, M, Andres, AM, Angelini, S, Ann, D, Anozie, UC, Ansari, MY, Antas, P, Antebi, A, Antón, Z, Anwar, T, Apetoh, L, Apostolova, N, Araki, T, Araki, Y, Arasaki, K, Araújo, WL, Araya, J, Arden, C, Arévalo, M-A, Arguelles, S, Arias, E, Arikkath, J, Arimoto, H, Ariosa, AR, Armstrong-James, D, Arnauné-Pelloquin, L, Aroca, A, Arroyo, DS, Arsov, I, Artero, R, Asaro, DML, Aschner, M, Ashrafizadeh, M, Ashur-Fabian, O, Atanasov, AG, Au, AK, Auberger, P, Auner, HW, Aurelian, L, Autelli, R, Avagliano, L, Ávalos, Y, Aveic, S, Aveleira, CA, Avin-Wittenberg, T, Aydin, Y, Ayton, S, Ayyadevara, S, Azzopardi, M, Baba, M, Backer, JM, Backues, SK, Bae, D-H, Bae, O-N, Bae, SH, Baehrecke, EH, Baek, A, Baek, S-H, Baek, SH, Bagetta, G, Bagniewska-Zadworna, A, Bai, H, Bai, J, Bai, X, Bai, Y, Bairagi, N, Baksi, S, Balbi, T, Baldari, CT, Balduini, W, Ballabio, A, Ballester, M, Balazadeh, S, Balzan, R, Bandopadhyay, R, Banerjee, S, Bánréti, Á, Bao, Y, Baptista, MS, Baracca, A, Barbati, C, Bargiela, A, Barilà, D, Barlow, PG, Barmada, SJ, Barreiro, E, Barreto, GE, Bartek, J, Bartel, B, Bartolome, A, Barve, GR, Basagoudanavar, SH, Bassham, DC, Bast, RC, Basu, A, Batoko, H, Batten, I, Baulieu, EE, Baumgarner, BL, Bayry, J, Beale, R, Beau, I, Beaumatin, F, Bechara, LRG, Beck, GR, Beers, MF, Begun, J, Behrends, C, Behrens, GMN, Bei, R, Bejarano, E, Bel, S, Behl, C, Belaid, A, Belgareh-Touzé, N, Bellarosa, C, Belleudi, F, Belló Pérez, M, Bello-Morales, R, Beltran, JSDO, Beltran, S, Benbrook, DM, Bendorius, M, Benitez, BA, Benito-Cuesta, I, Bensalem, J, Berchtold, MW, Berezowska, S, Bergamaschi, D, Bergami, M, Bergmann, A, Berliocchi, L, Berlioz-Torrent, C, Bernard, A, Berthoux, L, Besirli, CG, Besteiro, S, Betin, VM, Beyaert, R, Bezbradica, JS, Bhaskar, K, Bhatia-Kissova, I, Bhattacharya, R, Bhattacharya, S, Bhattacharyya, S, Bhuiyan, MS, Bhutia, SK, Bi, L, Bi, X, Biden, TJ, Bijian, K, Billes, VA, Binart, N, Bincoletto, C, Birgisdottir, AB, Bjorkoy, G, Blanco, G, Blas-Garcia, A, Blasiak, J, Blomgran, R, Blomgren, K, Blum, JS, Boada-Romero, E, Boban, M, Boesze-Battaglia, K, Boeuf, P, Boland, B, Bomont, P, Bonaldo, P, Bonam, SR, Bonfili, L, Bonifacino, JS, Boone, BA, Bootman, MD, Bordi, M, Borner, C, Bornhauser, BC, Borthakur, G, Bosch, J, Bose, S, Botana, LM, Botas, J, Boulanger, CM, Boulton, ME, Bourdenx, M, Bourgeois, B, Bourke, NM, Bousquet, G, Boya, P, Bozhkov, PV, Bozi, LHM, Bozkurt, TO, Brackney, DE, Brandts, CH, Braun, RJ, Braus, GH, Bravo-Sagua, R, Bravo-San Pedro, JM, Brest, P, Bringer, M-A, Briones-Herrera, A, Broaddus, VC, Brodersen, P, Brodsky, JL, Brody, SL, Bronson, PG, Bronstein, JM, Brown, CN, Brown, RE, Brum, PC, Brumell, JH, Brunetti-Pierri, N, Bruno, D, Bryson-Richardson, RJ, Bucci, C, Buchrieser, C, Bueno, M, Buitrago-Molina, LE, Buraschi, S, Buch, S, Buchan, JR, Buckingham, EM, Budak, H, Budini, M, Bultynck, G, Burada, F, Burgoyne, JR, Burón, MI, Bustos, V, Büttner, S, Butturini, E, Byrd, A, Cabas, I, Cabrera-Benitez, S, Cadwell, K, Cai, J, Cai, L, Cai, Q, Cairó, M, Calbet, JA, Caldwell, GA, Caldwell, KA, Call, JA, Calvani, R, Calvo, AC, Calvo-Rubio Barrera, M, Camara, NO, Camonis, JH, Camougrand, N, Campanella, M, Campbell, EM, Campbell-Valois, F-X, Campello, S, Campesi, I, Campos, JC, Camuzard, O, Cancino, J, Candido de Almeida, D, Canesi, L, Caniggia, I, Canonico, B, Cantí, C, Cao, B, Caraglia, M, Caramés, B, Carchman, EH, Cardenal-Muñoz, E, Cardenas, C, Cardenas, L, Cardoso, SM, Carew, JS, Carle, GF, Carleton, G, Carloni, S, Carmona-Gutierrez, D, Carneiro, LA, Carnevali, O, Carosi, JM, Carra, S, Carrier, A, Carrier, L, Carroll, B, Carter, AB, Carvalho, AN, Casanova, M, Casas, C, Casas, J, Cassioli, C, Castillo, EF, Castillo, K, Castillo-Lluva, S, Castoldi, F, Castori, M, Castro, AF, Castro-Caldas, M, Castro-Hernandez, J, Castro-Obregon, S, Catz, SD, Cavadas, C, Cavaliere, F, Cavallini, G, Cavinato, M, Cayuela, ML, Cebollada Rica, P, Cecarini, V, Cecconi, F, Cechowska-Pasko, M, Cenci, S, Ceperuelo-Mallafré, V, Cerqueira, JJ, Cerutti, JM, Cervia, D, Cetintas, VB, Cetrullo, S, Chae, H-J, Chagin, AS, Chai, C-Y, Chakrabarti, G, Chakrabarti, O, Chakraborty, T, Chami, M, Chamilos, G, Chan, DW, Chan, EYW, Chan, ED, Chan, HYE, Chan, HH, Chan, H, Chan, MTV, Chan, YS, Chandra, PK, Chang, C-P, Chang, C, Chang, H-C, Chang, K, Chao, J, Chapman, T, Charlet-Berguerand, N, Chatterjee, S, Chaube, SK, Chaudhary, A, Chauhan, S, Chaum, E, Checler, F, Cheetham, ME, Chen, C-S, Chen, G-C, Chen, J-F, Chen, LL, Chen, L, Chen, M, Chen, M-K, Chen, N, Chen, Q, Chen, R-H, Chen, S, Chen, W, Chen, X-M, Chen, X-W, Chen, X, Chen, Y, Chen, Y-G, Chen, Y-J, Chen, Y-Q, Chen, ZS, Chen, Z, Chen, Z-H, Chen, ZJ, Cheng, H, Cheng, J, Cheng, S-Y, Cheng, W, Cheng, X, Cheng, X-T, Cheng, Y, Cheng, Z, Cheong, H, Cheong, JK, Chernyak, BV, Cherry, S, Cheung, CFR, Cheung, CHA, Cheung, K-H, Chevet, E, Chi, RJ, Chiang, AKS, Chiaradonna, F, Chiarelli, R, Chiariello, M, Chica, N, Chiocca, S, Chiong, M, Chiou, S-H, Chiramel, AI, Chiurchiù, V, Cho, D-H, Choe, S-K, Choi, AMK, Choi, ME, Choudhury, KR, Chow, NS, Chu, CT, Chua, JP, Chua, JJE, Chung, H, Chung, KP, Chung, S, Chung, S-H, Chung, Y-L, Cianfanelli, V, Ciechomska, IA, Cifuentes, M, Cinque, L, Cirak, S, Cirone, M, Clague, MJ, Clarke, R, Clementi, E, Coccia, EM, Codogno, P, Cohen, E, Cohen, MM, Colasanti, T, Colasuonno, F, Colbert, RA, Colell, A, Čolić, M, Coll, NS, Collins, MO, Colombo, MI, Colón-Ramos, DA, Combaret, L, Comincini, S, Cominetti, MR, Consiglio, A, Conte, A, Conti, F, Contu, VR, Cookson, MR, Coombs, KM, Coppens, I, Corasaniti, MT, Corkery, DP, Cordes, N, Cortese, K, Costa, MDC, Costantino, S, Costelli, P, Coto-Montes, A, Crack, PJ, Crespo, JL, Criollo, A, Crippa, V, Cristofani, R, Csizmadia, T, Cuadrado, A, Cui, B, Cui, J, Cui, Y, Culetto, E, Cumino, AC, Cybulsky, AV, Czaja, MJ, Czuczwar, SJ, D'Adamo, S, D'Amelio, M, D'Arcangelo, D, D'Lugos, AC, D'Orazi, G, da Silva, JA, Dafsari, HS, Dagda, RK, Dagdas, Y, Daglia, M, Dai, X, Dai, Y, Dal Col, J, Dalhaimer, P, Dalla Valle, L, Dallenga, T, Dalmasso, G, Damme, M, Dando, I, Dantuma, NP, Darling, AL, Das, H, Dasarathy, S, Dasari, SK, Dash, S, Daumke, O, Dauphinee, AN, Davies, JS, Dávila, VA, Davis, RJ, Davis, T, Dayalan Naidu, S, De Amicis, F, De Bosscher, K, De Felice, F, De Franceschi, L, De Leonibus, C, de Mattos Barbosa, MG, De Meyer, GRY, De Milito, A, De Nunzio, C, De Palma, C, De Santi, M, De Virgilio, C, De Zio, D, Debnath, J, DeBosch, BJ, Decuypere, J-P, Deehan, MA, Deflorian, G, DeGregori, J, Dehay, B, Del Rio, G, Delaney, JR, Delbridge, LMD, Delorme-Axford, E, Delpino, MV, Demarchi, F, Dembitz, V, Demers, ND, Deng, H, Deng, Z, Dengjel, J, Dent, P, Denton, D, DePamphilis, ML, Der, CJ, Deretic, V, Descoteaux, A, Devis, L, Devkota, S, Devuyst, O, Dewson, G, Dharmasivam, M, Dhiman, R, di Bernardo, D, Di Cristina, M, Di Domenico, F, Di Fazio, P, Di Fonzo, A, Di Guardo, G, Di Guglielmo, GM, Di Leo, L, Di Malta, C, Di Nardo, A, Di Rienzo, M, Di Sano, F, Diallinas, G, Diao, J, Diaz-Araya, G, Díaz-Laviada, I, Dickinson, JM, Diederich, M, Dieudé, M, Dikic, I, Ding, S, Ding, W-X, Dini, L, Dinić, J, Dinic, M, Dinkova-Kostova, AT, Dionne, MS, Distler, JHW, Diwan, A, Dixon, IMC, Djavaheri-Mergny, M, Dobrinski, I, Dobrovinskaya, O, Dobrowolski, R, Dobson, RCJ, Đokić, J, Dokmeci Emre, S, Donadelli, M, Dong, B, Dong, X, Dong, Z, Dorn Ii, GW, Dotsch, V, Dou, H, Dou, J, Dowaidar, M, Dridi, S, Drucker, L, Du, A, Du, C, Du, G, Du, H-N, Du, L-L, du Toit, A, Duan, S-B, Duan, X, Duarte, SP, Dubrovska, A, Dunlop, EA, Dupont, N, Durán, RV, Dwarakanath, BS, Dyshlovoy, SA, Ebrahimi-Fakhari, D, Eckhart, L, Edelstein, CL, Efferth, T, Eftekharpour, E, Eichinger, L, Eid, N, Eisenberg, T, Eissa, NT, Eissa, S, Ejarque, M, El Andaloussi, A, El-Hage, N, El-Naggar, S, Eleuteri, AM, El-Shafey, ES, Elgendy, M, Eliopoulos, AG, Elizalde, MM, Elks, PM, Elsasser, H-P, Elsherbiny, ES, Emerling, BM, Emre, NCT, Eng, CH, Engedal, N, Engelbrecht, A-M, Engelsen, AST, Enserink, JM, Escalante, R, Esclatine, A, Escobar-Henriques, M, Eskelinen, E-L, Espert, L, Eusebio, M-O, Fabrias, G, Fabrizi, C, Facchiano, A, Facchiano, F, Fadeel, B, Fader, C, Faesen, AC, Fairlie, WD, Falcó, A, Falkenburger, BH, Fan, D, Fan, J, Fan, Y, Fang, EF, Fang, Y, Fanto, M, Farfel-Becker, T, Faure, M, Fazeli, G, Fedele, AO, Feldman, AM, Feng, D, Feng, J, Feng, L, Feng, Y, Feng, W, Fenz Araujo, T, Ferguson, TA, Fernández, ÁF, Fernandez-Checa, JC, Fernández-Veledo, S, Fernie, AR, Ferrante, AW, Ferraresi, A, Ferrari, MF, Ferreira, JCB, Ferro-Novick, S, Figueras, A, Filadi, R, Filigheddu, N, Filippi-Chiela, E, Filomeni, G, Fimia, GM, Fineschi, V, Finetti, F, Finkbeiner, S, Fisher, EA, Fisher, PB, Flamigni, F, Fliesler, SJ, Flo, TH, Florance, I, Florey, O, Florio, T, Fodor, E, Follo, C, Fon, EA, Forlino, A, Fornai, F, Fortini, P, Fracassi, A, Fraldi, A, Franco, B, Franco, R, Franconi, F, Frankel, LB, Friedman, SL, Fröhlich, LF, Frühbeck, G, Fuentes, JM, Fujiki, Y, Fujita, N, Fujiwara, Y, Fukuda, M, Fulda, S, Furic, L, Furuya, N, Fusco, C, Gack, MU, Gaffke, L, Galadari, S, Galasso, A, Galindo, MF, Gallolu Kankanamalage, S, Galluzzi, L, Galy, V, Gammoh, N, Gan, B, Ganley, IG, Gao, F, Gao, H, Gao, M, Gao, P, Gao, S-J, Gao, W, Gao, X, Garcera, A, Garcia, MN, Garcia, VE, García-Del Portillo, F, Garcia-Escudero, V, Garcia-Garcia, A, Garcia-Macia, M, García-Moreno, D, Garcia-Ruiz, C, García-Sanz, P, Garg, AD, Gargini, R, Garofalo, T, Garry, RF, Gassen, NC, Gatica, D, Ge, L, Ge, W, Geiss-Friedlander, R, Gelfi, C, Genschik, P, Gentle, IE, Gerbino, V, Gerhardt, C, Germain, K, Germain, M, Gewirtz, DA, Ghasemipour Afshar, E, Ghavami, S, Ghigo, A, Ghosh, M, Giamas, G, Giampietri, C, Giatromanolaki, A, Gibson, GE, Gibson, SB, Ginet, V, Giniger, E, Giorgi, C, Girao, H, Girardin, SE, Giridharan, M, Giuliano, S, Giulivi, C, Giuriato, S, Giustiniani, J, Gluschko, A, Goder, V, Goginashvili, A, Golab, J, Goldstone, DC, Golebiewska, A, Gomes, LR, Gomez, R, Gómez-Sánchez, R, Gomez-Puerto, MC, Gomez-Sintes, R, Gong, Q, Goni, FM, González-Gallego, J, Gonzalez-Hernandez, T, Gonzalez-Polo, RA, Gonzalez-Reyes, JA, González-Rodríguez, P, Goping, IS, Gorbatyuk, MS, Gorbunov, NV, Görgülü, K, Gorojod, RM, Gorski, SM, Goruppi, S, Gotor, C, Gottlieb, RA, Gozes, I, Gozuacik, D, Graef, M, Gräler, MH, Granatiero, V, Grasso, D, Gray, JP, Green, DR, Greenhough, A, Gregory, SL, Griffin, EF, Grinstaff, MW, Gros, F, Grose, C, Gross, AS, Gruber, F, Grumati, P, Grune, T, Gu, X, Guan, J-L, Guardia, CM, Guda, K, Guerra, F, Guerri, C, Guha, P, Guillén, C, Gujar, S, Gukovskaya, A, Gukovsky, I, Gunst, J, Günther, A, Guntur, AR, Guo, C, Guo, H, Guo, L-W, Guo, M, Gupta, P, Gupta, SK, Gupta, S, Gupta, VB, Gupta, V, Gustafsson, AB, Gutterman, DD, H B, R, Haapasalo, A, Haber, JE, Hać, A, Hadano, S, Hafrén, AJ, Haidar, M, Hall, BS, Halldén, G, Hamacher-Brady, A, Hamann, A, Hamasaki, M, Han, W, Hansen, M, Hanson, PI, Hao, Z, Harada, M, Harhaji-Trajkovic, L, Hariharan, N, Haroon, N, Harris, J, Hasegawa, T, Hasima Nagoor, N, Haspel, JA, Haucke, V, Hawkins, WD, Hay, BA, Haynes, CM, Hayrabedyan, SB, Hays, TS, He, C, He, Q, He, R-R, He, Y-W, He, Y-Y, Heakal, Y, Heberle, AM, Hejtmancik, JF, Helgason, GV, Henkel, V, Herb, M, 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Y, Oshima, S, Rong, Y, Sluimer, JC, Stallings, CL, and Tong, C-K
Abstract: In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.
Published: 2021

8. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Author: Klionsky, D, Abdel-Aziz, A, Abdelfatah, S, Abdellatif, M, Abdoli, A, Abel, S, Abeliovich, H, Abildgaard, M, Abudu, Y, Acevedo-Arozena, A, Adamopoulos, I, Adeli, K, Adolph, T, Adornetto, A, Aflaki, E, Agam, G, Agarwal, A, Aggarwal, B, Agnello, M, Agostinis, P, Agrewala, J, Agrotis, A, Aguilar, P, Ahmad, S, Ahmed, Z, Ahumada-Castro, U, Aits, S, Aizawa, S, Akkoc, Y, Akoumianaki, T, Akpinar, H, Al-Abd, A, Al-Akra, L, Al-Gharaibeh, A, Alaoui-Jamali, M, Alberti, S, Alcocer-Gómez, E, Alessandri, C, Ali, M, Alim Al-Bari, M, Aliwaini, S, Alizadeh, J, Almacellas, E, Almasan, A, Alonso, A, Alonso, G, Altan-Bonnet, N, Altieri, D, Álvarez, É, Alves, S, Alves da Costa, C, Alzaharna, M, Amadio, M, Amantini, C, Amaral, C, Ambrosio, S, Amer, A, Ammanathan, V, An, Z, Andersen, S, Andrabi, S, Andrade-Silva, M, Andres, A, Angelini, S, Ann, D, Anozie, U, Ansari, M, Antas, P, Antebi, A, Antón, Z, Anwar, T, Apetoh, L, Apostolova, N, Araki, T, Araki, Y, Arasaki, K, Araújo, W, Araya, J, Arden, C, 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Josephine W, Thirumalaikumar, V P, Thomas, Sufi Mary, Thomes, Paul G, Thorburn, Andrew, Thukral, Lipi, Thum, Thomas, Thumm, Michael, Tian, Ling, Tichy, Ales, Till, Andreas, Timmerman, Vincent, Titorenko, Vladimir I, Todi, Sokol V, Todorova, Krassimira, Toivonen, Janne M, Tomaipitinca, Luana, Tomar, Dhanendra, Tomas-Zapico, Cristina, Tomić, Sergej, Tong, Benjamin Chun-Kit, Tong, Chao, Tong, Xin, Tooze, Sharon A, Torgersen, Maria L, Torii, Satoru, Torres-López, Liliana, Torriglia, Alicia, Towers, Christina G, Towns, Roberto, Toyokuni, Shinya, Trajkovic, Vladimir, Tramontano, Donatella, Tran, Quynh-Giao, Travassos, Leonardo H, Trelford, Charles B, Tremel, Shirley, Trougakos, Ioannis P, Tsao, Betty P, Tschan, Mario P, Tse, Hung-Fat, Tse, Tak Fu, Tsugawa, Hitoshi, Tsvetkov, Andrey S, Tumbarello, David A, Tumtas, Yasin, Tuñón, María J, Turcotte, Sandra, Turk, Boris, Turk, Vito, Turner, Bradley J, Tuxworth, Richard I, Tyler, Jessica K, Tyutereva, Elena V, Uchiyama, Yasuo, Ugun-Klusek, 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Alexandre T, Victor, Victor M, Vidal, Michel, Vidoni, Chiara, Vieira, Otilia V, Vierstra, Richard D, Viganó, Sonia, Vihinen, Helena, Vijayan, Vinoy, Vila, Miquel, Vilar, Marçal, Villalba, José M, Villalobo, Antonio, Villarejo-Zori, Beatriz, Villarroya, Francesc, Villarroya, Joan, Vincent, Olivier, Vindis, Cecile, Viret, Christophe, Viscomi, Maria Teresa, Visnjic, Dora, Vitale, Ilio, Vocadlo, David J, Voitsekhovskaja, Olga V, Volonté, Cinzia, Volta, Mattia, Vomero, Marta, Von Haefen, Clarissa, Vooijs, Marc A, Voos, Wolfgang, Vucicevic, Ljubica, Wade-Martins, Richard, Waguri, Satoshi, Waite, Kenrick A, Wakatsuki, Shuji, Walker, David W, Walker, Mark J, Walker, Simon A, Walter, Jochen, Wandosell, Francisco G, Wang, Bo, Wang, Chao-Yung, Wang, Chen, Wang, Chenran, Wang, Chenwei, Wang, Cun-Yu, Wang, Dong, Wang, Fangyang, Wang, Feng, Wang, Fengming, Wang, Guansong, Wang, Han, Wang, Hao, Wang, Hexiang, Wang, Hong-Gang, Wang, Jianrong, Wang, Jigang, Wang, Jiou, Wang, Jundong, Wang, Kui, Wang, Lianrong, Wang, Liming, Wang, Maggie Haitian, Wang, Meiqing, Wang, Nanbu, Wang, Pengwei, Wang, Peipei, Wang, Ping, Wang, Qing Jun, Wang, Qing, Wang, Qing Kenneth, Wang, Qiong A, Wang, Wen-Tao, Wang, Wuyang, Wang, Xinnan, Wang, Xuejun, Wang, Yan, Wang, Yanchang, Wang, Yanzhuang, Wang, Yen-Yun, Wang, Yihua, Wang, Yipeng, Wang, Yu, Wang, Yuqi, Wang, Zhe, Wang, Zhenyu, Wang, Zhouguang, Warnes, Gary, Warnsmann, Verena, Watada, Hirotaka, Watanabe, Eizo, Watchon, Maxinne, Wawrzyńska, Anna, Weaver, Timothy E, Wegrzyn, Grzegorz, Wehman, Ann M, Wei, Huafeng, Wei, Lei, Wei, Taotao, Wei, Yongjie, Weiergräber, Oliver H, Weihl, Conrad C, Weindl, Günther, Weiskirchen, Ralf, Wells, Alan, Wen, Runxia H, Wen, Xin, Werner, Antonia, Weykopf, Beatrice, Wheatley, Sally P, Whitton, J Lindsay, Whitworth, Alexander J, Wiktorska, Katarzyna, Wildenberg, Manon E, Wileman, Tom, Wilkinson, Simon, Willbold, Dieter, Williams, Brett, Williams, Robin S B, Williams, Roger L, Williamson, Peter R, Wilson, Richard 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Dun-Sheng, Yang, Huan, Yang, Huang-Tian, Yang, Hui, Yang, Jin-Ming, Yang, Jing, Yang, Jingyu, Yang, Ling, Yang, Liu, Yang, Ming, Yang, Pei-Ming, Yang, Qian, Yang, Seungwon, Yang, Shu, Yang, Shun-Fa, Yang, Wannian, Yang, Wei Yuan, Yang, Xiaoyong, Yang, Xuesong, Yang, Yi, Yang, Ying, Yao, Honghong, Yao, Shenggen, Yao, Xiaoqiang, Yao, Yong-Gang, Yao, Yong-Ming, Yasui, Takahiro, Yazdankhah, Meysam, Yen, Paul M, Yi, Cong, Yin, Xiao-Ming, Yin, Yanhai, Yin, Zhangyuan, Yin, Ziyi, Ying, Meidan, Ying, Zheng, Yip, Calvin K, Yiu, Stephanie Pei Tung, Yoo, Young H, Yoshida, Kiyotsugu, Yoshii, Saori R, Yoshimori, Tamotsu, Yousefi, Bahman, Yu, Boxuan, Yu, Haiyang, Yu, Jun, Yu, Li, Yu, Ming-Lung, Yu, Seong-Woon, Yu, Victor C, Yu, W Haung, Yu, Zhengping, Yu, Zhou, Yuan, Junying, Yuan, Ling-Qing, Yuan, Shilin, Yuan, Shyng-Shiou F, Yuan, Yanggang, Yuan, Zengqiang, Yue, Jianbo, Yue, Zhenyu, Yun, Jeanho, Yung, Raymond L, Zacks, David N, Zaffagnini, Gabriele, Zambelli, Vanessa O, Zanella, Isabella, Zang, Qun S, Zanivan, Sara, Zappavigna, Silvia, Zaragoza, Pilar, Zarbalis, Konstantinos S, Zarebkohan, Amir, Zarrouk, Amira, Zeitlin, Scott O, Zeng, Jialiu, Zeng, Ju-Deng, Žerovnik, Eva, Zhan, Lixuan, Zhang, Bin, Zhang, Donna D, Zhang, Hanlin, Zhang, Hong, Zhang, Honghe, Zhang, Huafeng, Zhang, Huaye, Zhang, Hui, Zhang, Hui-Ling, Zhang, Jianbin, Zhang, Jianhua, Zhang, Jing-Pu, Zhang, Kalin Y B, Zhang, Leshuai W, Zhang, Lin, Zhang, Lisheng, Zhang, Lu, Zhang, Luoying, Zhang, Menghuan, Zhang, Peng, Zhang, Sheng, Zhang, Wei, Zhang, Xiangnan, Zhang, Xiao-Wei, Zhang, Xiaolei, Zhang, Xiaoyan, Zhang, Xin, Zhang, Xinxin, Zhang, Xu Dong, Zhang, Yang, Zhang, Yanjin, Zhang, Yi, Zhang, Ying-Dong, Zhang, Yingmei, Zhang, Yuan-Yuan, Zhang, Yuchen, Zhang, Zhe, Zhang, Zhengguang, Zhang, Zhibing, Zhang, Zhihai, Zhang, Zhiyong, Zhang, Zili, Zhao, Haobin, Zhao, Lei, Zhao, Shuang, Zhao, Tongbiao, Zhao, Xiao-Fan, Zhao, Ying, Zhao, Yongchao, Zhao, Yongliang, Zhao, Yuting, Zheng, Guoping, Zheng, Kai, Zheng, Ling, Zheng, Shizhong, Zheng, Xi-Long, Zheng, Yi, Zheng, Zu-Guo, Zhivotovsky, Boris, Zhong, Qing, Zhou, Ao, Zhou, Ben, Zhou, Cefan, Zhou, Gang, Zhou, Hao, Zhou, Hong, Zhou, Hongbo, Zhou, Jie, Zhou, Jing, Zhou, Jiyong, Zhou, Kailiang, Zhou, Rongjia, Zhou, Xu-Jie, Zhou, Yanshuang, Zhou, Yinghong, Zhou, Yubin, Zhou, Zheng-Yu, Zhou, Zhou, Zhu, Binglin, Zhu, Changlian, Zhu, Guo-Qing, Zhu, Haining, Zhu, Hongxin, Zhu, Hua, Zhu, Wei-Guo, Zhu, Yanping, Zhu, Yushan, Zhuang, Haixia, Zhuang, Xiaohong, Zientara-Rytter, Katarzyna, Zimmermann, Christine M, Ziviani, Elena, Zoladek, Teresa, Zong, Wei-Xing, Zorov, Dmitry B, Zorzano, Antonio, Zou, Weiping, Zou, Zhen, Zou, Zhengzhi, Zuryn, Steven, Zwerschke, Werner, Brand-Saberi, Beate, Dong, X Charlie, Kenchappa, Chandra Shekar, Li, Zuguo, Lin, Yong, Oshima, Shigeru, Rong, Yueguang, Sluimer, Judith C, Stallings, Christina L, and Tong, Chun-Kit
Abstract: In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field.
Published: 2021

9. Hepatology: Portal vein cavernoma imitating cholangiocarcinoma in a patient with erythropoietic protoporphyria

Author: Saberi, B, Deurdulian, C, Pandya, H, and Kahn, JA
Published: 2014
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10. Outcomes of Liver Transplantation for Hereditary Hemorrhagic Telangiectasia (HHT).: Abstract# C1969

Author: Saberi, B., Heimbach, J., Larson, J., Raghavaiah, S., Krowka, M., Kamath, P., and Leise, M.
Published: 2014

11. Characterization of migration behavior of myogenic precursor cells in the limb bud with respect to Lmx1b expression

Author: Schweizer, H., Johnson, R. L., and Brand-Saberi, B.
Published: 2004
Full Text: View/download PDF

12. Expression of thymosin beta4 during chick development

Author: Dathe, V. and Brand-Saberi, B.
Published: 2004
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13. Expression of kinesin kif5c during chick development

Author: Dathe, V., Pröls, F., and Brand-Saberi, B.
Published: 2004
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14. Natural history of acute upper GI bleeding due to tumours: short-term success and long-term recurrence with or without endoscopic therapy

Author: Sheibani, S., Kim, J. J., Chen, B., Park, S., Saberi, B., Keyashian, K., Buxbaum, J., and Laine, L.
Published: 2013
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15. Brief Review on Some Neurological Diseases Which Have Association with Trinucleotide Repeat Sequences

Author: Saberi B
Subjects: General Engineering
Abstract: Trinucleotide repeat sequences can be seen in some neurological diseases. This study will briefly review some of these neurological diseases and the associated trinucleotide repeat sequences.
Published: 2021

16. cDermo-1 expression indicates a role in avian skin development

Author: Scaal, Martin, Füchtbauer, Ernst-Martin, and Brand-Saberi, B.
Published: 2001
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17. New experimental evidence for somite resegmentation

Author: Huang, R., Zhi, Q., Brand-Saberi, B., and Christ, B.
Published: 2000
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18. Pathophysiology of increased nuchal translucency in chromosomally abnormal fetuses

Author: von Kaisenberg, C. S., Nicolaides, K. H., Jonat, W., and Brand-Saberi, B.
Published: 1999
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19. Genetic and epigenetic control of muscle development in vertebrates

Author: Brand-Saberi, B. and Christ, Bodo
Published: 1999
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20. Expression of Lefty predicts Merkel cell carcinoma‐specific death

Author: Gambichler, T., primary, Ardabili, S., additional, Lang, K., additional, Dreißigacker, M., additional, Scheel, C., additional, Brand‐Saberi, B., additional, Skrygan, M., additional, Stockfleth, E., additional, Käfferlein, H.U., additional, Brüning, T., additional, and Becker, J.C., additional
Published: 2020
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21. Lymphatic capillary hypoplasia in the skin of fetuses with increased nuchal translucency and Turnerʼs syndrome: comparison with trisomies and controls

Author: von Kaisenberg, C.S., Wilting, J., Dörk, T., Nicolaides, K.H., Meinhold-Heerlein, I., Hillemanns, P., and Brand-Saberi, B.
Published: 2010
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22. Defect repair after somite removal in avian embryos is not true regeneration

Author: Jüngel-Waas, K., Christ, B., and Brand-Saberi, B.
Published: 1998
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23. Morphological classification of nuchal skin in human fetuses with trisomy 21, 18, and 13 at 12—18 weeks and in a trisomy 16 mouse

Author: von Kaisenberg, C. S., Krenn, V., Ludwig, M., Nicolaides, K. H., and Brand-Saberi, B.
Published: 1998
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24. Distribution of extracellular matrix components in nuchal skin from fetuses carrying trisomy 18 and trisomy 21

Author: Brand-Saberi, B., Epperlein, H. H., Romanos, G. E., and Christ, B.
Published: 1994
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25. Differences in the fibronectin-dependence of migrating cell populations

Author: Brand-Saberi, B., Krenn, V., Grim, M., and Christ, B.
Published: 1993
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26. Scatter factor/hepatocyte growth factor (SF/HGF) induces emigration of myogenic cells at interlimb level in vivo

Author: Brand-Saberi, B., Muller, T.S., Wilting, J., Christ, B., and Birchmeier, C.
Subjects: Myogenesis -- Research, Growth factors -- Research, Biological sciences
Published: 1996

27. Glycosaminoglycans and proteoglycans in the skin of aneuploid fetuses with increased nuchal translucency

Author: von Kaisenberg, C. S., Prols, F., Nicolaides, K. H., Maass, N., Meinhold-Heerlein, I., and Brand-Saberi, B.
Published: 2003

28. 1. Entwicklungsbiologische Grundlagen der Teratogenese

Author: Christ, B., primary, Brand-Saberi, B., additional, and Wilting, J., additional
Published: 1993
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29. 3:45 PM Abstract No. 276 Can pretransplant TACE improve overall posttransplant survival for patients with hepatocellular carcinoma?

Author: Buethe, J., primary, Werner, J., additional, Liddell, R., additional, Frangakis, C., additional, Ruck, J., additional, Hong, K., additional, Philosophe, B., additional, Cameron, A., additional, Saberi, B., additional, Gurakar, A., additional, and Georgiades, C., additional
Published: 2018
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30. THE ICE TEST FOR DIAGNOSING MYASTHENIA GRAVIS

Author: Tabassi, A., alireza dehghani, and Saberi, B.
Subjects: myasthenia gravis, lcsh:R5-920, Tensilon test, ice test, Ptosis, lcsh:Medicine (General)
Abstract: There are many tests for diagnosis of myasthenia gravis including Tensilon test and ice test.To compare the ice test with Tensilon test in sub jects with myasthenic and nonmyasthenic ptosis a process research study was designed. This study was performed in patients complaining of acquired ptosis in the neuro-ophthalmology center of Farabi Hospital. All 156 patients were tested with ice pack and edrophonium with an interval of 15 minutes. The patient was instructed to hold an ice filled plastic glove on the closed ptotic eyelid. Before and after 2 minutes of ice application on the ptotic eyelid, the distance between the upper and lower margin was measured by the neuro-ophthalmologist. An increase of 2 mm or hig her was considered a positive test result. Patients with positive Tensilon test were considered as control. In all 61 patients with positive Tensilon test the ice test was positive, and in none of the 95 patients with negative Tensilon test the ice test was positive. The ice test is a simple, fast, specific and sensitive test for the diagnosis of myasthenic ptosis.
Published: 2005

31. The control of directed myogenic cell migration in the avian limb bud

Author: Brand-Saberi, B., Krenn, V., and Christ, B.
Published: 1989
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32. Grundlagen der Limbusentwicklung im Hühnerembryo

Author: Chankiewitz, E., Chankiewitz, V., Theiß, C., Steuhl, K.-P., Meller, D., and Brand-Saberi, B.
Subjects: ddc: 610, 610 Medical sciences, Medicine
Abstract: Störungen der Limbusstammzellfunktion bedingen eine schwere Beeinträchtigung der Oberflächenintegrität des Auges, so dass die Sehfunktion beeinträchtigt wird. Die fehlende Regenerationsreserve des Hornhautepithels führt dabei zu einer Konjunktivalisierung, Vaskularisierung,[for full text, please go to the a.m. URL], 174. Versammlung des Vereins Rheinisch-Westfälischer Augenärzte
Published: 2012
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33. Wahlfach im vorklinischen Abschnitt an der Albert-Ludwigs-Universität Freiburg

Author: Brand-Saberi, B and Streitlein-Böhme, I
Subjects: ddc: 610
Published: 2005

34. CXCR4 and Gab1 cooperate to control the development of migrating muscle progenitor cells

Author: Vasyutina, E., Stebler, J., Brand-Saberi, B., Schulz, S., Raz, E., and Birchmeier, C.
Subjects: Function and Dysfunction of the Nervous System
Abstract: Long-range migrating progenitor cells generate hypaxial muscle, for instance the muscle of the limbs, hypoglossal cord, and diaphragm. We show here that migrating muscle progenitors express the chemokine receptor CXCR4. The corresponding ligand, SDF1, is expressed in limb and branchial arch mesenchyme; i.e., along the routes and at the targets of the migratory cells. Ectopic application of SDF1 in the chick limb attracts muscle progenitor cells. In CXCR4 mutant mice, the number of muscle progenitors that colonize the anlage of the tongue and the dorsal limb was reduced. Changes in the distribution of the muscle progenitor cells were accompanied by increased apoptosis, indicating that CXCR4 signals provide not only attractive cues but also control survival. Gab1 encodes an adaptor protein that transduces signals elicited by tyrosine kinase receptors, for instance the c-Met receptor, and plays a role in the migration of muscle progenitor cells. We found that CXCR4 and Gab1 interact genetically. For instance, muscle progenitors do not reach the anlage of the tongue in CXCR4;Gab1 double mutants; this target is colonized in either of the single mutants. Our analysis reveals a role of SDF1/CXCR4 signaling in the development of migrating muscle progenitors and shows that a threshold number of progenitor cells is required to generate muscle of appropriate size.
Published: 2005

35. Congenital myopathy with arrest of myogenesis prior to formation of myotubes

Author: Laberke Hg, Uhlenberg B, Wagner M, Heymut Omran, Brand-Saberi B, and U.-P. Ketelsen
Subjects: medicine.medical_specialty, Muscle Fibers, Skeletal, Neuromuscular Junction, MyoD, Muscle Development, Internal medicine, Medicine, Humans, Myopathy, Muscle, Skeletal, Neural Cell Adhesion Molecules, Myogenin, MyoD Protein, Myosin Heavy Chains, business.industry, Myogenesis, Cardiac muscle, Infant, Newborn, Skeletal muscle, General Medicine, medicine.disease, Congenital myopathy, Immunohistochemistry, Endocrinology, medicine.anatomical_structure, Pediatrics, Perinatology and Child Health, Myogenic regulatory factors, Female, Neurology (clinical), Laminin, medicine.symptom, business, Myopathies, Structural, Congenital
Abstract: We report a novel type of congenital myopathy, which is characterized by an early arrest of muscle formation prior to formation of myotubes. A female infant born prematurely at 32 weeks of gestational age died after six weeks of continuous ventilatory support. Various muscle specimens including quadriceps, deltoid, pectoral, neck, psoas, tongue, and diaphragm musculature were studied. Light and electron microscopy revealed well-demarcated fascicular structures interspersed with undifferentiated, mononuclear myogenic cells. Multinucleated myotubes and muscle fibres were not detectable, pointing towards a defect prior to the generation of myotubes during myogenesis. Immunohistochemistry identified the absence of dystrophin, N-CAM, MyoD and myogenin expression in these myogenic cells, compatible with a block of the complex transcriptional network necessary for correct embryonic muscle formation at an early stage of muscle development. These myopathological findings were absent in cardiac muscle, indicating that the defect exclusively affects skeletal muscle formation.
Published: 2005

36. Fehlbildungen

Author: Riede, U.N., primary and Brand-Saberi, B., additional
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37. Outcomes of Liver Transplantation for Hereditary Hemorrhagic Telangiectasia (HHT).

Author: Saberi, B., primary, Heimbach, J., additional, Larson, J., additional, Raghavaiah, S., additional, Krowka, M., additional, Kamath, P., additional, and Leise, M., additional
Published: 2014
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38. P3 Migration behaviour of myogenic precursor cells in the limb bud with respect to dorsoventral patterning

Author: Schweizer, H, Johnson, RL, and Brand-Saberi, B
Subjects: Proceedings of the Anatomical Society of Great Britain and Ireland
Published: 2002

39. c-Dermol expression is upregulated by BMP signal

Author: Scaal, M., Füchtbauer, Ernst-Martin, and Brand-Saberi, B.
Published: 2001

40. Grundlagen der Limbusentwicklung im Hühnerembryo

Author: Chankiewitz, E, Chankiewitz, V, Theiß, C, Steuhl, KP, Meller, D, Brand-Saberi, B, Chankiewitz, E, Chankiewitz, V, Theiß, C, Steuhl, KP, Meller, D, and Brand-Saberi, B
Published: 2012

41. Histopathological, immunohistochemical criteria and confocal laser-scanning data of arthrofibrosis

Author: Ruppert, M., primary, Theiss, C., additional, Knöß, P., additional, Kendoff, D., additional, Krukemeyer, M.G., additional, Schröder, N., additional, Brand-Saberi, B., additional, Gehrke, T., additional, and Krenn, V., additional
Published: 2013
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42. Changes of cytokeratin expression in the epidermis with chronic venous insufficiency

Author: Peschen M, Grenz H, Lahayé T, Brand-Saberi B, Jc, Simon, Schöpf E, and Vanscheidt W
Subjects: Adult, Aged, 80 and over, Male, Venous Insufficiency, Biopsy, Antibodies, Monoclonal, Humans, Keratins, Female, Middle Aged, Fluorescent Antibody Technique, Indirect, Aged, Skin
Abstract: A specific, individual pattern of cytokeratins (Cks) is expressed by each epithelial cells as part of the cytoskeleton. Cks are established as markers of epidermal differentiation. Basal cells are characterized by CK5 and 14 expression, whereas CK 1, 10 and 11 are typical for the suprabasal compartment of normal epidermis. Here, we investigated changes of Pan-CK, CK 10, and CK 14 expression in the epidermis in various stages of chronic venous insufficiency (CVI).In punch biopsies of 24 patients with chronic venous insufficiency and of 6 volunteers with normal skin Cks were detected by indirect immunofluorescence using monoclonal antibodies against CK 10, CK 14 and Pan-CK.CK 10 and Pan-CK staining intensity increased with the severity of CVI changes. Suprabasal cells showed an upregulation of CK 10 and Pan-CK expression first in venous eczema. CK 14 expression is under normal condition confined to the basal cell layer of the epidermis. However in venous eczema and lipodermatosclerosis, CK 14 is detected in the suprabasal epidermal compartment.It is therefore concluded that altered differentiation and stratification mechanisms occur in keratinocytes in the epidermis with CVI first detectable in the stage of venous eczema. These changes are accompanied by a characteristic CK expression pattern.
Published: 1997

43. Das Mentorenprogramm

Author: Brand-Saberi, B, Streitlein-Böhme, I, Brand-Saberi, B, and Streitlein-Böhme, I
Published: 2005

44. Genetische Analyse entwicklungsbiologischer Funktionen des Neuregulin-1/ErbB Signalsystems

Author: Brand-Saberi, B., Stehle, J. H., Britsch, Stefan, Brand-Saberi, B., Stehle, J. H., and Britsch, Stefan
Abstract: Neureguline (NDF, Heregulin, GGF ARIA, oder SMDF) sind EGF-ähnliche, extrazelluläre Signalmoleküle, die mit transmembranären Tyrosinkinaserezeptoren der ErbB-Familie interagieren. Neuregulin-1/ErbB Signale steuern während der Embryonalentwicklung und im adulten Organismus vielfältige zelluläre Prozesse, wie z. B. Proliferation, Migration und Differenzierung. In der vorliegenden Arbeit wurde die Rolle des Neuregulin-1/ErbB Signalsystems in der Entwicklung von Neuralleistenzellen und sich daraus entwickelnden Komponenten des peripheren Nervensystems (sympathisches Nervensystem und periphere Glia) untersucht. Neuregulin-1 Signale werden in Neuralleistenzellen und ihren Gliaderivaten durch ErbB2/ErbB3 Rezeptor-Heterodimere übertragen. Mit Hilfe von Mäusen mit gezielter Mutation (knock-out) des Neuregulin-1, ErbB2 oder ErbB3 Gens wurde gezeigt, daß Neuregulin-1/ErbB2/3 Signale die Migration sympathogener Neuralleistenzellen steuern. Mutante Tiere entwickeln daher eine hochgradige Hypoplasie des sympathischen Nervensystems. Neuregulin-1 Signale kontrollieren darüber hinaus die Entwicklung von Schwann Zellen. Die Unterbrechung des Neuregulin-1/ErbB2/3 Signalwegs in mutanten Mäusen führt zum Verlust von Schwann Zellen während der Embryogenese. Es wurde außerdem gezeigt, daß der Transkriptionsfaktor Sox10 die Expression von ErbB3 in Neuralleistenzellen kontrolliert. Sox10 und ErbB3 Mutanten besitzen daher übereinstimmende Defekte in der Neuralleistenzellentwicklung. Neben den ErbB3-abhängigen Funktionen von Sox10 wurde eine ErbB3-unabhängige Schlüsselfunktion von Sox10 bei der Differenzierung von Neuralleistenzellen zu peripherer Glia identifiziert. Das Neuregulin-1/ErbB2/3 Signalsystem und der Transkriptionsfaktor Sox10 besitzen also gemeinsam zentrale Funktionen in der Entwicklung peripherer Glia, steuern diesen Prozess aber über unterschiedliche Mechanismen und während unterschiedlicher Entwicklungsphasen. Sox10, ErbB2 und ErbB3 mutante Mäuse entwickeln neben dem Verlust, Neuregulins (NDF, heregulin, GGF ARIA, or SMDF) are EGF-like growth and differentiation factors that signal through tyrosine kinase receptors of the erbB family. The neuregulin-1 proteins and their receptors play essential roles during embryonic development and in the adult. Functions of the neuregulin/erbB signaling system in developing neural crest cells and their derivatives (sympathetic nervous system, peripheral glial cells) were analyzed in mice with targeted mutations in the erbB2, erbB3, or neuregulin-1 genes. All three mutations cause severe hypoplasia of the primary sympathetic ganglion chain, and migration of sympathogenic neural crest cells to their target sites, where they differentiate into sympathetic neurons, depends on neuregulin-1 and its receptors. Neuregulin-1 signals are also essential for the development of Schwann cells. As a consequence, mice with targeted mutations in the neuregulin-1/erbB signaling system completely lack Schwann cells. Moreover, the HMG-box transcription factor sox10 is shown to control expression of erbB3 in neural crest cells. In accordance, sox10 and erbB3 mutant mice share phenotypes in the developing neural crest. Additionally, a novel, erbB3-independent developmental function of sox10 was identified: Sox10 is a key regulator for glial fate determination in undifferentiated neural crest cells. Thus, the transcription factor sox10 and the neuregulin-1/erbB signalling system both serve critical functions during development of peripheral glial cells. However, they act via different cellular mechanisms and during different developmental stages. At later developmental stages lack of peripheral glial cells in sox10, erbB2 and erbB3 mutant mice results in a severe degeneration of sensory and motor neurons. The comparison of the mutant phenotypes demonstrates, that peripheral glial cells generate essential signals for the survival and maintenance of accompanying neurons.
Published: 2004

45. Congenital Myopathy with Arrest of Myogenesis Prior to Formation of Myotubes

Author: Ketelsen, U.-P., primary, Brand-Saberi, B., additional, Uhlenberg, B., additional, Wagner, M., additional, Laberke, H.-G., additional, and Omran, H., additional
Published: 2005
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46. The scoliosis (sco) mouse: a new allele of Pax1

Author: Adham, I.M., primary, Gille, M., additional, Gamel, A.J., additional, Reis, A., additional, Dressel, R., additional, Steding, G., additional, Brand-Saberi, B., additional, and Engel, W., additional
Published: 2005
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47. Blut- und Lymphgefäße bei Feten mit erhöhter Nackentransparenz von 11 - 14 Schwangerschaftswochen: ein Review

Author: von Kaisenberg, C. S., primary, Nicolaides, K. H., additional, and Brand-Saberi, B., additional
Published: 2004
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48. Development of the vertebral column: Morphogenesis and genes

Author: Wilting, J, Müller, T S, Ebensperger, C, Brand-Saberi, B, Christ, B, Neubüser, A, Balling, Rudi, Koseki, H, Wilting, J, Müller, T S, Ebensperger, C, Brand-Saberi, B, Christ, B, Neubüser, A, Balling, Rudi, and Koseki, H
Published: 1996

49. Pax-1, a regulator of sclerotome development is induced by notochord and floor plate signals in avian embryos.

Author: Ebensperger, C., Wilting, J., Brand-Saberi, B., Mizutani, Y., Christ, B., Balling, Rudi, Koseki, H., Ebensperger, C., Wilting, J., Brand-Saberi, B., Mizutani, Y., Christ, B., Balling, Rudi, and Koseki, H.
Abstract: Pax-1 encodes for a DNA-binding transcriptional activator that was originally discovered in murine embryos using a probe from the Drosophila paired-box-containing gene, gooseberry-distal. We have cloned the avian Pax-1 gene as a basis for experimental studies of the induction of Pax-1 in the paraxial mesoderm. The amino acid sequence of the paired-domain is exactly the same in the quail and mouse, whereas outside the paired-domain there is 61% homology. Starting at about the eight-somite stage, quail Pax-1 is expressed in the paraxial mesoderm in a craniocaudal sequence. The unsegmented paraxial mesoderm and the two most recently formed somites do not express Pax-1. In the epithelial somite, the somitocoele cells and the cells of the ventral two-thirds of the epithelial wall are positive. As soon as the sclerotome is formed, only a subset of sclerotome cells expresses Pax-1. These are the cells that migrate towards the notochord to form the perinotochordal tube. Expression then becomes restricted to the intervertebral discs, the perichondrium of the vertebral bodies and the connective tissue surrounding the spinal ganglia. Additional expression domains are found in the scapula and the pelvic region, distinct areas of the head, and the epithelium of the second to the fourth visceral pouch. In later stages the thymus is positive. In vitro and in vivo experiments show that the notochord induces Pax-1 in the paraxial mesoderm, but limb bud mesoderm is not competent to respond to notochordal signals. Floor plate is also capable of inducing Pax-1 expression in sclerotome cells. Our studies show that in competent cells of the paraxial mesoderm, Pax-1 is a mediator of signals emanating from the notochord and the floor plate.
Published: 1995
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50. WS10: Chromosomopathies WS10-01Pathophysiology of increased nuchal translucency-abnormalities of the extracellular matrix

Author: Von Kaisenberg, C.S., primary, Jonat, W., additional, Brand-Saberi, B., additional, Farzaneh, F., additional, and Nicolaides, K.H., additional
Published: 2000
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