The WNK1 and WNK4 protein kinases that are mutated in Gordon's hypertension syndrome phosphorylate and activate SPAK and OSR1 protein kinases

Mutations in the human genes encoding WNK1 [with no K (lysine) protein kinase-1] and the related protein kinase WNK4 are the cause of Gordon's hypertension syndrome. Little is known about the molecular mechanism by which WNK isoforms regulate cellular processes. We immunoprecipitated WNK1 from...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Vitari, Alberto C., Deak, Maria, Morrice, Nick A., Alessi, Dario R.
Médium: Artigo
Jazyk:Inglês
Vydáno: Portland Press Ltd. 2005
Témata:
Accelerated Publication
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1237134/
https://ncbi.nlm.nih.gov/pubmed/16083423
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20051180
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky