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المؤلفون: Jue-Sheng Ong, René Thieme, Janusz Jankowski, Jiyuan An, Anne C. Böhmer, Stuart MacGregor, David C. Whiteman, Johannes Schumacher, Claire Palles, Rachel E. Neale, Matthew Law, Puya Gharahkhani, Ines Gockel, John Lai, Catherine M. Olsen, Xikun Han, Beacon, Rebecca C. Fitzgerald, Tom L. Vaughan
المساهمون: Gharahkhani, Puya [0000-0002-4203-5952], Law, Matthew H [0000-0002-4303-8821], Ong, Jue-Sheng [0000-0002-6062-710X], Han, Xikun [0000-0002-3823-7308], Olsen, Catherine M [0000-0003-4483-1888], Böhmer, Anne C [0000-0002-5716-786X], Fitzgerald, Rebecca C [0000-0002-3434-3568], MacGregor, Stuart [0000-0001-6731-8142], Apollo - University of Cambridge Repository
المصدر: Nature Communications, Vol 10, Iss 1, Pp 1-10 (2019)
Nature Communicationsمصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Science, General Physics and Astronomy, Genome-wide association study, Disease, Esophageal Diseases, Genome-wide association studies, Polymorphism, Single Nucleotide, Gastroenterology, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, Gastro-oesophageal reflux disease, Internal medicine, Humans, Medicine, Genetic Predisposition to Disease, Allele, Esophagus, Risk factor, lcsh:Science, Cancer genetics, Multidisciplinary, business.industry, Esophageal disease, Oesophageal cancer, General Chemistry, medicine.disease, humanities, digestive system diseases, 3. Good health, 030104 developmental biology, medicine.anatomical_structure, Genetic Loci, 030220 oncology & carcinogenesis, Gastroesophageal Reflux, GERD, Adenocarcinoma, lcsh:Q, Female, business, Genome-Wide Association Study
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a530542f0d7f586e929d882bc728eb4dTest
https://doaj.org/article/69989b38dc994e248ea97c1493de2f41Test -
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المؤلفون: Lisa S. Kearns, Helena Liang, Nona Farbehi, Xikun Han, Alex W. Hewitt, Drew Neavin, Grace E. Lidgerwood, Stuart MacGregor, M Isabel G Lopez Sanchez, Lerna Gulluyan, Damián Hernández, David A. Mackey, Angela Steinmann, Linda Clarke, Vivek Gupta, Louise A. Rooney, Joseph E. Powell, Alice Pébay, Chia-Ling Chan, Robyn H. Guymer, Ran Zhang, Joao A. Paulo, Maciej Daniszewski, Guy Bylsma, Uyen Nguyen, Vikkitharan Gnanasambandapillai, Rachael Zekanovic, Anne Senabouth, Nitin Verma, Mehdi Mirzaei
المصدر: Nature communications. 13(1)
مصطلحات موضوعية: Genetics, Proteomics, Multidisciplinary, Retinal pigment epithelium, Neurodegeneration, General Physics and Astronomy, General Chemistry, Retinal Pigment Epithelium, Biology, Macular degeneration, Quantitative trait locus, medicine.disease, General Biochemistry, Genetics and Molecular Biology, Transcriptome, Macular Degeneration, medicine.anatomical_structure, Geographic Atrophy, Expression quantitative trait loci, medicine, Humans, sense organs, Induced pluripotent stem cell
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49df11c858c66f28265e3899aa36f2d7Test
https://pubmed.ncbi.nlm.nih.gov/35882847Test -
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المؤلفون: Shea Ping Yip, Patrick Y. P. Kao, Fumihiko Matsuda, Hideo Nakanishi, Maria Schache, Tien Yin Wong, Satoshi Morooka, Kyoko Ohno-Matsui, Ozen Polasek, Kenji Yamashiro, Akitaka Tsujikawa, Zhenglin Yang, Chiea Chuen Khor, E-Shyong Tai, Norimoto Gotoh, Yumiko Akagi-Kurashige, Peng Chen, Stuart MacGregor, David A. Mackey, Isao Nakata, Alan F. Wright, Akira Meguro, Seang-Mei Saw, Maurice Yap, Fan Qiao, Yasuharu Tabara, Paul N. Baird, Muka Moriyama, Caroline Hayward, Ching-Yu Cheng, Luling Huang, Andrea J. Richardson, Nobuhisa Mizuki, Veronique Vitart, Yi Shi, Alex W. Hewitt, Sentaro Kusuhara, Tin Aung, Harry Campbell, Kim Hung Leung, Masaki Takeuchi, Gabriel Cuellar, Kenji Suda, Masahiro Miyake, Ryo Yamada, Nagahisa Yoshimura
المصدر: Miyake, M, Yamashiro, K, Tabara, Y, Suda, K, Morooka, S, Nakanishi, H, Khor, C-C, Chen, P, Qiao, F, Nakata, I, Akagi-Kurashige, Y, Gotoh, N, Tsujikawa, A, Meguro, A, Kusuhara, S, Polasek, O, Hayward, C, Wright, A F, Campbell, H, Richardson, A J, Schache, M, Takeuchi, M, Mackey, D A, Hewitt, A W, Cuellar, G, Shi, Y, Huang, L, Yang, Z, Leung, K H, Kao, P Y P, Yap, M K H, Yip, S P, Moriyama, M, Ohno-Matsui, K, Mizuki, N, MacGregor, S, Vitart, V, Aung, T, Saw, S-M, Tai, E-S, Wong, T Y, Cheng, C-Y, Baird, P N, Yamada, R & Matsuda, F & Yoshimura, N 2015, ' Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia ', Nature Communications, vol. 6, 6689 . https://doi.org/10.1038/ncomms7689Test
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, genetic structures, Adolescent, Genotype, General Physics and Astronomy, Animals, Asian Continental Ancestry Group, Cohort Studies, Cornea, Disease Models, Animal, European Continental Ancestry Group, Female, Genetic Predisposition to Disease, Humans, Immunohistochemistry, Mice, Middle Aged, Myopia, Polymorphism, Single Nucleotide, Proto-Oncogene Proteins, Retina, RNA, Messenger, Severity of Illness Index, Wnt Proteins, Young Adult, Genome-wide association study, General Biochemistry, Genetics and Molecular Biology, White People, Asian People, Polymorphism (computer science), Ophthalmology, Severity of illness, medicine, Young adult, Multidisciplinary, business.industry, General Chemistry, Odds ratio, eye diseases, medicine.anatomical_structure, Choroidal neovascularization, sense organs, medicine.symptom, business
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54c98516bbd4611cfefdd1d755849650Test
https://pubmed.ncbi.nlm.nih.gov/25823570Test