Diabetes insipidus in mice with a mutation in aquaporin-2. - Wikidata - awgldk - TriplyDB

Diabetes insipidus in mice with a mutation in aquaporin-2.

Diabetes insipidus in mice with a mutation in aquaporin-2.

http://www.wikidata.org/entity/Q24814986

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Reduced cholesterol and triglycerides in mice with a mutation in Mia2, a liver protein that localizes to ER exit sites The Trafficking of the Water Channel Aquaporin-2 in Renal Principal Cells-a Potential Target for Pharmacological Intervention in Cardiovascular Diseases A gain-of-function mutation in adenylate cyclase 3 protects mice from diet-induced obesity Data and animal management software for large-scale phenotype screening.Nephrogenic diabetes insipidus in mice caused by deleting COOH-terminal tail of aquaporin-2.Claudin-4 deficiency results in urothelial hyperplasia and lethal hydronephrosis.Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation.The epithelial sodium/proton exchanger, NHE3, is necessary for renal and intestinal calcium (re)absorption Regulation of transport in the connecting tubule and cortical collecting duct Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.Mouse models and the urinary concentrating mechanism in the new millennium.Hsp90 inhibitor partially corrects nephrogenic diabetes insipidus in a conditional knock-in mouse model of aquaporin-2 mutation.Physiology and pathophysiology of the vasopressin-regulated renal water reabsorption.Dissecting the roles of aquaporins in renal pathophysiology using transgenic mice.Beta1-integrin is required for kidney collecting duct morphogenesis and maintenance of renal function.Congenital nephrogenic diabetes insipidus: what can we learn from mouse models?Genetic and developmental basis for urinary tract obstruction.A selective EP4 PGE2 receptor agonist alleviates disease in a new mouse model of X-linked nephrogenic diabetes insipidus.Inactivation of Notch signaling in the renal collecting duct causes nephrogenic diabetes insipidus in mice.Hyperactivation of Nrf2 in early tubular development induces nephrogenic diabetes insipidus.Cell culture models and animal models for studying the patho-physiological role of renal aquaporins.Congenital nephrogenic diabetes insipidus: the current state of affairs.Molecular physiology of the medullary collecting duct.Dynamic regulation and dysregulation of the water channel aquaporin-2: a common cause of and promising therapeutic target for water balance disorders.Characterization of V71M mutation in the aquaporin-2 gene causing nephrogenic diabetes insipidus.Hereditary Nephrogenic Diabetes Insipidus: Pathophysiology and Possible Treatment. An Update.Development and performances of a Japanese quail line homozygous for the diabetes insipidus (di) mutation.

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P2860

Diabetes insipidus in mice with a mutation in aquaporin-2.

http://www.wikidata.org/entity/Q24814986

description

2005 nî lūn-bûn

@nan

2005 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

@zh-hans

2005年学术文章

@zh-my

2005年学术文章

@zh-sg

2005年學術文章

@yue

name

Diabetes insipidus in mice with a mutation in aquaporin-2

@nl

Diabetes insipidus in mice with a mutation in aquaporin-2.

@ast

Diabetes insipidus in mice with a mutation in aquaporin-2.

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type

label

Diabetes insipidus in mice with a mutation in aquaporin-2

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Diabetes insipidus in mice with a mutation in aquaporin-2.

@ast

Diabetes insipidus in mice with a mutation in aquaporin-2.

@en

prefLabel

Diabetes insipidus in mice with a mutation in aquaporin-2

@nl

Diabetes insipidus in mice with a mutation in aquaporin-2.

@ast

Diabetes insipidus in mice with a mutation in aquaporin-2.

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JOURNAL.PGEN.0010020

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Diabetes insipidus in mice with a mutation in aquaporin-2.

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P2093

David J Lloyd

http://www.w3.org/2001/XMLSchema#string

Frank Wesley Hall

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Lisa M Tarantino

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Nicholas Gekakis

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P2860

Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin-CD water channels to plasma membrane

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene

Requirement of human renal water channel aquaporin-2 for vasopressin-dependent concentration of urine

Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus

Oligosaccharyl transferase: gatekeeper to the secretory pathway

Inositol (1,4,5) trisphosphate 3 kinase B controls positive selection of T cells and modulates Erk activity

Severely impaired urinary concentrating ability in transgenic mice lacking aquaporin-1 water channels

Erythrocyte water permeability and renal function in double knockout mice lacking aquaporin-1 and aquaporin-3

Heteroligomerization of an Aquaporin-2 mutant with wild-type Aquaporin-2 and their misrouting to late endosomes/lysosomes explains dominant nephrogenic diabetes insipidus.

Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing.

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e20

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scholarly article

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10.1371/JOURNAL.PGEN.0010020

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