-
1دورية أكاديمية
المؤلفون: Shaika Shanbagh, Jyoti Matalia, Ramaraj Kannan, Rohit Shetty, Pratibha Panmand, Sumitha O Muthu, Shyam S Chaurasia, Vrushali Deshpande, Shomi S Bhattacharya, Abilash V Gopalakrishnan, Arkasubhra Ghosh
المصدر: Indian Journal of Ophthalmology, Vol 71, Iss 5, Pp 2143-2151 (2023)
مصطلحات موضوعية: cataract, fibrosis, gene expression, lens, transcription factors, Ophthalmology, RE1-994
وصف الملف: electronic resource
-
2دورية أكاديمية
المؤلفون: Naushin H Waseem, Sancy Low, Amna Z Shah, Deepa Avisetti, Pia Ostergaard, Michael Simpson, Katarzyna A Niemiec, Belen Martin-Martin, Hebah Aldehlawi, Saima Usman, Pak Sang Lee, Anthony P Khawaja, Jonathan B Ruddle, Ameet Shah, Ege Sackey, Alexander Day, Yuzhen Jiang, Geoff Swinfield, Ananth Viswanathan, Giovanna Alfano, Christina Chakarova, Heather J Cordell, David F Garway-Heath, Peng T Khaw, Shomi S Bhattacharya, Ahmad Waseem, Paul J Foster
المصدر: PLoS Genetics, Vol 16, Iss 4, p e1008721 (2020)
وصف الملف: electronic resource
-
3دورية أكاديمية
المؤلفون: Barbara Czub, Amna Z Shah, Giovanna Alfano, Przemysław M Kruczek, Christina F Chakarova, Shomi S Bhattacharya
المصدر: PLoS ONE, Vol 11, Iss 2, p e0148678 (2016)
وصف الملف: electronic resource
-
4دورية أكاديمية
المؤلفون: Giovanna Alfano, Przemyslaw M Kruczek, Amna Z Shah, Barbara Kramarz, Glen Jeffery, Andrew C Zelhof, Shomi S Bhattacharya
المصدر: PLoS ONE, Vol 11, Iss 11, p e0166397 (2016)
وصف الملف: electronic resource
-
5دورية أكاديمية
المؤلفون: Dunja eLukovic, Victoria eMoreno-Manzano, Martin eKlabusay, Miodrag eStojkovic, Shomi S Bhattacharya, SLAVEN eERCEG
المصدر: Frontiers in Genetics, Vol 5 (2014)
مصطلحات موضوعية: Pluripotent Stem Cells, differentiation, human embryonic stem cells, non coding RNA, pluripotency, Genetics, QH426-470
وصف الملف: electronic resource
-
6دورية أكاديمية
المؤلفون: Monisha E Nongpiur, Chiea Chuen Khor, Hongyan Jia, Belinda K Cornes, Li-Jia Chen, Chunyan Qiao, K Saidas Nair, Ching-Yu Cheng, Liang Xu, Ronnie George, Do Tan, Khaled Abu-Amero, Shamira A Perera, Mineo Ozaki, Takanori Mizoguchi, Yasuo Kurimoto, Sancy Low, Liza-Sharmini A Tajudin, Ching-Lin Ho, Clement C Y Tham, Ileana Soto, Paul T K Chew, Hon-Tym Wong, Balekudaru Shantha, Masako Kuroda, Essam A Osman, Guangxian Tang, Sujie Fan, Hailin Meng, Hua Wang, Bo Feng, Victor H K Yong, Serena M L Ting, Yang Li, Ya-Xing Wang, Zheng Li, Raghavan Lavanya, Ren-Yi Wu, Ying-Feng Zheng, Daniel H Su, Seng-Chee Loon, Vernon K Y Yong, R Rand Allingham, Michael A Hauser, Nagaswamy Soumittra, Vedam L Ramprasad, Naushin Waseem, Azhany Yaakub, Kee-Seng Chia, Govindasamy Kumaramanickavel, Tina T Wong, Alicia C How, Tran Nguyen Bich Chau, Cameron P Simmons, Jin-Xin Bei, Yi-Xin Zeng, Shomi S Bhattacharya, Mingzhi Zhang, Donald T Tan, Yik-Ying Teo, Saleh A Al-Obeidan, Do Nhu Hon, E-Shyong Tai, Seang-Mei Saw, Paul J Foster, Lingam Vijaya, Jost B Jonas, Tien-Yin Wong, Simon W M John, Chi-Pui Pang, Eranga N Vithana, Ningli Wang, Tin Aung
المصدر: PLoS Genetics, Vol 10, Iss 3, p e1004089 (2014)
وصف الملف: electronic resource
-
7دورية أكاديمية
المؤلفون: Giulia Venturini, Anna M Rose, Amna Z Shah, Shomi S Bhattacharya, Carlo Rivolta
المصدر: PLoS Genetics, Vol 8, Iss 11, p e1003040 (2012)
وصف الملف: electronic resource
-
8دورية أكاديمية
المؤلفون: Petra Liskova, Rhian Gwilliam, Martin Filipec, Katerina Jirsova, Stanislava Reinstein Merjava, Panos Deloukas, Tom R Webb, Shomi S Bhattacharya, Neil D Ebenezer, Alex G Morris, Alison J Hardcastle
المصدر: PLoS ONE, Vol 7, Iss 9, p e45495 (2012)
وصف الملف: electronic resource
-
9
المؤلفون: İlhan E. Acar, Laura Lores-Motta, Johanna M. Colijn, Magda A. Meester-Smoor, Timo Verzijden, Audrey Cougnard-Gregoire, Soufiane Ajana, Benedicte M.J. Merle, Anita de Breuk, Thomas J. Heesterbeek, Erik van den Akker, Mohamed R. Daha, Birte Claes, Daniel Pauleikhoff, Hans-Werner Hense, Cornelia M. van Duijn, Sascha Fauser, Carel B. Hoyng, Cécile Delcourt, Caroline C.W. Klaver, Tessel E. Galesloot, Anneke I. den Hollander, Blanca Arango-Gonzalez, Angela Armento, Franz Badura, Vaibhav Bhatia, Shomi S. Bhattacharya, Marc Biarnés, Anna Borrell, Sofia M. Calado, Sascha Dammeier, Berta De la Cerda, Francisco J. Diaz-Corrales, Sigrid Diether, Eszter Emri, Tanja Endermann, Lucia L. Ferraro, Míriam Garcia, Sabina Honisch, Ellen Kilger, Elod Kortvely, Claire Lastrucci, Hanno Langen, Imre Lengyel, Phil Luthert, Jordi Monés, Everson Nogoceke, Tunde Peto, Frances M. Pool, Eduardo Rodriguez-Bocanegra, Luis Serrano, Jose Sousa, Eric Thee, Marius Ueffing, Karl U. Ulrich Bartz-Schmidt, Markus Zumbansen
المصدر: Ophthalmology. 127:1693-1709
مصطلحات موضوعية: Apolipoprotein E, Very low-density lipoprotein, genetic structures, Metabolite, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Metabolomics, Metabolome, Medicine, 030304 developmental biology, Genetic association, 2. Zero hunger, Genetics, 0303 health sciences, biology, business.industry, Case-control study, eye diseases, 3. Good health, Ophthalmology, chemistry, ABCA1, 030221 ophthalmology & optometry, biology.protein, sense organs, business
-
10
المؤلفون: Wassila Carpentier, Thierry Léveillard, Christine Lonjou, Jean-Paul Saraiva, Christel Condroyer, Saddek Mohand-Said, Shomi S. Bhattacharya, Hélène Dollfus, Maria Solaguren-Beascoa, Vanessa Démontant, Lisa Emmenegger, Marie-Elise Lancelot, Elise Orhan, Kinga M. Bujakowska, Christelle Michiels, Marion Neuillé, José-Alain Sahel, Isabelle Audo, Cécile Méjécase, Eric A. Pierce, Mélanie Letexier, Christina Zeitz, Aline Antonio
المساهمون: Ministère de l’Enseignement supérieur et de la Recherche (France), Fondation de France, Foundation Fighting Blindness, Fondation Voir et Entendre, Agence Nationale de la Recherche (France), National Eye Institute (US), Région Ile-de-France, Association Française contre les Myopathies
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instname
Clin Genetمصطلحات موضوعية: Adult, Male, 0301 basic medicine, Candidate gene, WD40 Repeats, genetic structures, WDR34, Whole-exomesequencing, 030105 genetics & heredity, Biology, medicine.disease_cause, Article, 03 medical and health sciences, Retinitis pigmentosa, Genetics, Rod-cone dystrophy, medicine, Humans, Genetic Association Studies, Genetics (clinical), Exome sequencing, Non-syndromic rod-cone dystrophy, Mutation, Dystrophy, Disease gene identification, medicine.disease, Pedigree, KIAA2026, Ciliopathy, 030104 developmental biology, sense organs, Carrier Proteins, Cone-Rod Dystrophies