Cargando…
STK39 and WNK1 Are Potential Hypertension Susceptibility Genes in the BELHYPGEN Cohort
The serine/threonine kinase With-No-Lysine (K) Kinase 1 (WNK1) activates the thiazide-sensitive Na(+)/Cl(−) cotransporter through phosphorylation of STE20/SPS1-related proline/alanine-rich kinase, another serine/threonine kinase encoded by STK39. The aim of this study was to look for association bet...
Autores principales: | Persu, Alexandre, Evenepoel, Lucie, Jin, Yu, Mendola, Antonella, Ngueta, Gérard, Yang, Wen-Yi, Gruson, Damien, Horman, Sandrine, Staessen, Jan A., Vikkula, Miikka |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839787/ https://www.ncbi.nlm.nih.gov/pubmed/27082544 http://dx.doi.org/10.1097/MD.0000000000002968 |
Ejemplares similares
-
A meta-analytical assessment of STK39 three well-defined polymorphisms in susceptibility to hypertension
por: Yang, Hualing, et al.
Publicado: (2016) -
Relationship of SELE A561C and G98T Variants With the Susceptibility to CAD
por: Liao, Bihong, et al.
Publicado: (2016) -
Association of polymorphisms of preptin, irisin and adropin genes with susceptibility to coronary artery disease and hypertension
por: Wang, Haidong, et al.
Publicado: (2020) -
Connection of GLI1 variants to congenital heart disease susceptibility: A case-control study
por: Guan, Weiwei, et al.
Publicado: (2020) -
Genomics of Fibromuscular Dysplasia
por: Di Monaco, Silvia, et al.
Publicado: (2018)