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Genomics|June 1, 1997
Human cholecystokinin type A receptor gene: cytogenetic localization, physical mapping, and identification of two missense variants in patients with obesity and non-insulin-dependent diabetes mellitus (NIDDM)H Inoue, C A Iannotti, C M Welling, et al.
Diabetologia|September 8, 2010
Conditional ablation of Gsk-3β in islet beta cells results in expanded mass and resistance to fat feeding-induced diabetes in miceY Liu, K Tanabe, D Baronnier, et al.
Diabetologia|December 29, 1998
Missense mutations in the pancreatic islet beta cell inwardly rectifying K+ channel gene (KIR6.2/BIR): a meta-analysis suggests a role in the polygenic basis of Type II diabetes mellitus in CaucasiansE H Hani, P Boutin, E Durand, et al.
Genomics|July 1, 1992
Mapping the human liver/islet glucose transporter (GLUT2) gene within a genetic linkage map of chromosome 3q using a (CA)n dinucleotide repeat polymorphism and characterization of the polymorphism in three racial groupsA Matsutani, A Hing, T Steinbrueck, et al.
The Journal of Clinical Investigation|December 1, 1984
Polymorphism in the 5' flanking region of the human insulin gene. Relationships with noninsulin-dependent diabetes mellitus, glucose and insulin concentrations, and diabetes treatment in the Pima IndiansW C Knowler, D J Pettitt, B Vasquez, et al.
The American Journal of Physiology|October 1, 1990
Glucose transporter protein content and glucose transport capacity in rat skeletal musclesE J Henriksen, R E Bourey, K J Rodnick, et al.
Diabetologia|April 1, 1996
A human pancreatic islet inwardly rectifying potassium channel: cDNA cloning, determination of the genomic structure and genetic variations in Japanese NIDDM patientsY Tanizawa, A Matsubara, K Ueda, et al.
The Journal of Clinical Investigation|May 1, 1984
An in vivo analysis of pancreatic protein and insulin biosynthesis in a rat model for non-insulin-dependent diabetesM A Permutt, K Kakita, P Malinas, et al.
Human Mutation|August 14, 1999
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinismB Glaser, J Furth, C A Stanley, et al.
Diabetes|July 2, 1998
Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancyS L Shyng, T Ferrigni, J B Shepard, et al.
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