Mutation of Fnip1 is associated with B-cell deficiency, cardiomyopathy, and elevated AMPK activity

Folliculin (FLCN) is a tumor-suppressor protein mutated in the Birt–Hogg–Dubé (BHD) syndrome, which associates with two paralogous proteins, folliculin-interacting protein (FNIP)1 and FNIP2, forming a complex that interacts with the AMP-activated protein kinase (AMPK). Although it is clear that this...

Descrizione completa

Salvato in:
Dettagli Bibliografici
Pubblicato in:Proc Natl Acad Sci U S A
Autori principali: Siggs, Owen M., Stockenhuber, Alexander, Deobagkar-Lele, Mukta, Bull, Katherine R., Crockford, Tanya L., Kingston, Bethany L., Crawford, Greg, Anzilotti, Consuelo, Steeples, Violetta, Ghaffari, Sahar, Czibik, Gabor, Bellahcene, Mohamed, Watkins, Hugh, Ashrafian, Houman, Davies, Benjamin, Woods, Angela, Carling, David, Yavari, Arash, Beutler, Bruce, Cornall, Richard J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: National Academy of Sciences 2016
Soggetti:
PNAS Plus
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4932993/
https://ncbi.nlm.nih.gov/pubmed/27303042
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1607592113
Tags: Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !

Documenti analoghi