Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus
- 1 July 2015
- journal article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 97 (1) , 177-185
Abstract
No abstract availableKeywords
This publication has 34 references indexed in Scilit:
- Many faces of monogenic diabetesJournal of Diabetes Investigation, 2014
- Joint Effect of Insulin Signaling Genes on Insulin Secretion and Glucose HomeostasisThe Journal of Clinical Endocrinology & Metabolism, 2013
- A solid quality-control analysis of AB SOLiD short-read sequencing dataBriefings in Bioinformatics, 2012
- The Mammalian Tribbles Homolog TRIB3, Glucose Homeostasis, and Cardiovascular DiseasesEndocrine Reviews, 2012
- MODYDiabetes Care, 2011
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing dataGenome Research, 2010
- Subcellular membrane curvature mediated by the BAR domain superfamily proteinsSeminars in Cell & Developmental Biology, 2010
- The endoplasmic reticulum in pancreatic beta cells of type 2 diabetes patientsDiabetologia, 2007
- Crystal Structures of the BAR-PH and PTB Domains of Human APPL1Structure, 2007
- Phenotypic characteristics of early-onset autosomal-dominant type 2 diabetes unlinked to known maturity-onset diabetes of the young (MODY) genes.Diabetes Care, 1999