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Notch signaling regulates Akap12 expression and primary cilia length during renal tubule morphogenesis.

Alagille syndrome patients present with loss of function mutations in either JAG1 or NOTCH2. About 40-50% of patients have kidney abnormalities, and frequently display multi-cystic, dysplastic kidneys. Additionally, gain-of-function mutations in NOTCH2 are associated with cystic kidneys in Hajdu-Che...

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Bibliografski detalji
Izdano u:FASEB J
Glavni autori: Mukherjee, Malini, Ratnayake, Ishara, Janga, Madhusudhana, Fogarty, Eric, Scheidt, Shania, Grassmeyer, Justin, deRiso, Jennifer, Chandrasekar, Indra, Ahrenkiel, Phil, Kopan, Raphael, Surendran, Kameswaran
Format: Artigo
Jezik:Inglês
Izdano: 2020
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC7501208/
https://ncbi.nlm.nih.gov/pubmed/32474964
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1096/fj.201902358RR
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