Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Sclerosis and NR3C1[original query] |
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Sequencing analysis of the human glucocorticoid receptor (NR3C1) gene in multiple sclerosis patients. Journal of the neurological sciences 2016 Apr 363 165-9. Kassi Eva, Semaniakou Anna, Sertedaki Amalia, Evangelopoulos Maria-Eleftheria, Kazazoglou Theodosia, Kominakis Antonios, Sfagos Constantinos, Charmandari Evangelia, Chrousos George P, Moutsatsou Paraske |
Functional fine-mapping of noncoding risk variants in amyotrophic lateral sclerosis utilizing convolutional neural network. Scientific reports 2020 8 10 (1): 12872. Yousefian-Jazi Ali, Sung Min Kyung, Lee Taeyeop, Hong Yoon-Ho, Choi Jung Kyoon, Choi Jinwo |
Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population.
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2021 3 73 (10): 1860-1870. Jamieson Sarra E, Fakiola Michaela, Tang Dave, Scaman Elizabeth, Syn Genevieve, Francis Richard W, Coates Harvey L, Anderson Denise, Lassmann Timo, Cordell Heather J, Blackwell Jenefer |
ABCB1 gene polymorphisms impact the effect of high-dose intravenous methylprednisolone therapy on optic neuritis associated with AQP4-IgG-positive neuromyelitis optica spectrum disorder. Journal of clinical pharmacy and therapeutics 2022 4 47 (9): 1379-1387. Dai Yuyang, Ni Siyang, Wu Feng, Guo Shaojie, Zhao Xiuli, Wang Jiaw |
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- Page last updated:Apr 22, 2024
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