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Systems Genetics in Human Endothelial Cells Identifies Non-coding Variants Modifying Enhancers, Expression, and Complex Disease Traits

The identification of causal variants and mechanisms underlying complex disease traits in humans is important for the progress of human disease genetics; this requires finding strategies to detect functional regulatory variants in disease-relevant cell types. To achieve this, we collected genetic an...

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Detaylı Bibliyografya
Yayımlandı:Am J Hum Genet
Asıl Yazarlar: Stolze, Lindsey K., Conklin, Austin C., Whalen, Michael B., López Rodríguez, Maykel, Õunap, Kadri, Selvarajan, Ilakya, Toropainen, Anu, Örd, Tiit, Li, Jin, Eshghi, Anna, Solomon, Alice E., Fang, Yun, Kaikkonen, Minna U., Romanoski, Casey E.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Elsevier 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7273528/
https://ncbi.nlm.nih.gov/pubmed/32442411
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2020.04.008
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