Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Disease and GAP43[original query] |
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| Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease. Journal of cellular and molecular medicine 2018 Apr . Wang Yang, Yan Weihui, Wang Jun, Zhou Ying, Chen Jie, Gu Beilin, Cai W |
Genome-wide association study for proliferative diabetic retinopathy in Africans.
NPJ genomic medicine 2019 4 20. Liu Chang, Chen Guanjie, Bentley Amy R, Doumatey Ayo, Zhou Jie, Adeyemo Adebowale, Yang Jinkui, Rotimi Charl |
| Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Aging 2020 3 12 (5): 4379-4393. Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W |
| Apolipoprotein B is a novel marker for early tau pathology in Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association 2021 9 18 (5): 875-887. Picard Cynthia, Nilsson Nathalie, Labonté Anne, Auld Daniel, Rosa-Neto Pedro, , Ashton Nicholas J, Zetterberg Henrik, Blennow Kaj, Breitner John C B, Villeneuve Sylvia, Poirier Judes, |
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