Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

V2R mutations and nephrogenic diabetes insipidus.

Progress in molecular biology and translational science - 1 Jan 2009

Bichet Daniel G

Abstract excerpt

Nephrogenic diabetes insipidus (NDI), which can be inherited or acquired, is characterized by an inability to concentrate urine despite normal or elevated plasma concentrations of the antidiuretic hormone, arginine vasopressin (AVP). Polyuria, with hyposthenuria, and polydipsia are the cardinal clinical manifestations of the disease. Nephrogenic failure to concentrate urine maximally may be due to a defect in...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Diabetes Insipidus, Nephrogenic
Share to Genetic Predisposition to Disease
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Mutant Proteins

Share to Mutation

Share to Protein Folding

Share to Protein Transport

Share to Receptors, Vasopressin

Source

Identifiers

PMID: 20374732
DOI: 10.1016/S1877-1173(09)89002-9

Genes

AVP
AQP2
AVPR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

V2R mutations and nephrogenic diabetes insipidus.PMID 20374732Read ↗

Nephrogenic diabetes insipidus.Semantic proximity Read ↗

Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant).Semantic proximity Read ↗

Nephrogenic diabetes insipidus.Semantic proximity Read ↗

Genetic basis of nephrogenic diabetes insipidus.Semantic proximity Read ↗

Hereditary Nephrogenic Diabetes Insipidus: Pathophysiology and Possible Treatment. An Update.Semantic proximity Read ↗

A Novel Mutation in the AVPR2 Gene Causing Congenital Nephrogenic Diabetes InsipidusSemantic proximity Read ↗

GENETICS IN ENDOCRINOLOGY Pathophysiology, diagnosis and treatment of familial nephrogenic diabetes insipidus.Semantic proximity Read ↗

Nephrogenic diabetes insipidus.Semantic proximity Read ↗

Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.Semantic proximity Read ↗

Aquaporin-2 water channel mutations causing nephrogenic diabetes insipidus.Semantic proximity Read ↗

Aquaporin 2 mutations in nephrogenic diabetes insipidus.Semantic proximity Read ↗

Physiopathology and diagnosis of nephrogenic diabetes insipidus.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.