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...

Полное описание

Сохранить в:
Библиографические подробности
Опубликовано в: :Proc Natl Acad Sci U S A
Главные авторы: 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.
Формат: Artigo
Язык:Inglês
Опубликовано: National Academy of Sciences 2016
Предметы:
PNAS Plus
Online-ссылка: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
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы