Phenotypic Characterization of Mice Carrying Homozygous Deletion of KLF11, a Gene in Which Mutations Cause Human Neonatal and MODY VII Diabetes

We have previously shown that amino acid changes in the human Kruppel-Like Factor (KLF) 11 protein is associated with the development of maturity onset diabetes of the young VII, whereas complete inactivation of this pathway by the −331 human insulin mutation causes neonatal diabetes mellitus. Here,...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Endocrinology
मुख्य लेखकों: Mathison, Angela, Escande, Carlos, Calvo, Ezequiel, Seo, Seungmae, White, Thomas, Salmonson, Ann, Faubion, William A., Buttar, Navtej, Iovanna, Juan, Lomberk, Gwen, Chini, Eduardo N., Urrutia, Raul
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Endocrine Society 2015
विषय:
Original Research
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC4588811/
https://ncbi.nlm.nih.gov/pubmed/26248217
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/en.2015-1145
टैग : टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!

समान संसाधन