diabetes mutation

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'diabetes mutation' can also refer to...

diabetes mutation

Relapsing diabetes can result from moderately activating mutations in KCNJ11

Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus—update and epidemiology

A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes

Functional effects of KCNJ11 mutations causing neonatal diabetes: enhanced activation by MgATP

WFS1 mutations are frequent monogenic causes of juvenile-onset diabetes mellitus in Lebanon

Typical type 2 diabetes mellitus and HFE gene mutations: a population-based case – control study

Characterization of a Nonsense Mutation in the Ceruloplasmin Gene Resulting in Diabetes and Neurodegenerative Disease

A de novo novel missense mutation in AVPR2 with severe nephrogenic diabetes insipidus

Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1β

A Newborn with Transient Diabetes Mellitus Accompanied by Ketoacidosis Attributable to a ZFP57 Mutation

Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy and Deafness (DIDMOAD) Caused by Mutations in a Novel Gene (Wolframin) Coding for a Predicted Transmembrane Protein

Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability

Mitochondrial DNA heteroplasmy in diabetes and normal adults: role of acquired and inherited mutational patterns in twins

Interaction between mutations in the slide helix of Kir6.2 associated with neonatal diabetes and neurological symptoms

Identification of Nine Novel Mutations in the Hepatocyte Nuclear Factor 1 Alpha Aene Associated with Maturity-Onset Diabetes of the Young (MODY3)

Identification and Characterization of Aquaporin-2 Water Channel Mutations Causing Nephrogenic Diabetes Insipidus with Partial Vasopressin Response

A novel mutation in AVPR2 causing congenital nephrogenic diabetes insipidus with complete resistance to antidiuretic hormone

Functional characterization of novel loss-of-function mutations in the vasopressin type 2 receptor gene causing nephrogenic diabetes insipidus


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Quick Reference

A mutation first identified in mice that spontaneously develop diabetic symptoms. It appears to be a mutation in the leptin receptor gene.

Subjects: Chemistry.

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