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Novel Thrombotic Function of a Human SNP in STXBP5 Revealed by CRISPR-Cas9 Gene Editing in Mice

OBJECTIVE: To identify and characterize the effect of a single nucleotide polymorphism (SNP) in the STXBP5 locus that is associated with altered thrombosis in humans. Genome wide association studies (GWAS) have identified numerous SNPs associated with human thrombotic phenotypes, but determining the...

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Detalhes bibliográficos
Publicado no:Arterioscler Thromb Vasc Biol
Main Authors: Zhu, Qiuyu Martin, Ko, Kyung Ae, Ture, Sara, Mastrangelo, Michael A., Chen, Ming-Huei, Johnson, Andrew D., O’Donnell, Christopher J., Morrell, Craig N., Miano, Joseph M., Lowenstein, Charles J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5269475/
https://ncbi.nlm.nih.gov/pubmed/28062498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/ATVBAHA.116.308614
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