Lataa...

Identification of common genetic variants controlling transcript isoform variation in human whole blood

An understanding of the genetic variation underlying transcript splicing is essential to dissect the molecular mechanisms of common disease. The available evidence from splicing quantitative trait locus (sQTL) studies has been limited to small samples. We performed genome-wide screening to identify...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Nat Genet
Päätekijät: Zhang, Xiaoling, Joehanes, Roby, Chen, Brian H, Huan, Tianxiao, Ying, Saixia, Munson, Peter J, Johnson, Andrew D, Levy, Daniel, O’Donnell, Christopher J
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2015
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC8273720/
https://ncbi.nlm.nih.gov/pubmed/25685889
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.3220
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!