Aquaporin-2: new mutations responsible for autosomal-recessive nephrogenic diabetes insipidus-update and epidemiology. - Wikidata - awgldk - TriplyDB

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

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

http://www.wikidata.org/entity/Q35452558

about

Effect of Glycyrrhiza on the Diuretic Function of Euphorbia kansui: An Ascites Mouse Model Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus.Development and Diseases of the Collecting Duct System.A farewell editorial from the Clinical Kidney Journal's former Editor-in-Chief.Function of the membrane water channel aquaporin-5 in the salivary gland Plant and Mammal Aquaporins: Same but Different.Diabetes Insipidus.The Expanding Role of Vesicles Containing Aquaporins

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P2860

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

http://www.wikidata.org/entity/Q35452558

description

2012 nî lūn-bûn

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2012 թուականի Մարտին հրատարակուած գիտական յօդուած

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2012 թվականի մարտին հրատարակված գիտական հոդված

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2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

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name

Aquaporin-2: new mutations res ...... pidus-update and epidemiology.

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Aquaporin-2: new mutations res ...... pidus-update and epidemiology.

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type

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Aquaporin-2: new mutations res ...... pidus-update and epidemiology.

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Aquaporin-2: new mutations res ...... pidus-update and epidemiology.

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Aquaporin-2: new mutations res ...... pidus-update and epidemiology.

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Aquaporin-2: new mutations res ...... pidus-update and epidemiology.

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Clinical kidney journal / an academic journal of the ERA-EDTA (European Renal Association - European Dialysis and Transplant Association)

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Aquaporin-2: new mutations res ...... ipidus-update and epidemiology

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P2093

Abdulah El Tarazi

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Detlef Bockenhauer

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Jessica Matar

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Marie-Françoise Arthus

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Michèle Lonergan

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Pierre Bissonnette

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Yoann Lussier

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P2860

Two novel mutations in the aquaporin-2 and the vasopressin V2 receptor genes in patients with congenital nephrogenic diabetes insipidus

An aquaporin-2 water channel mutant which causes autosomal dominant nephrogenic diabetes insipidus is retained in the Golgi complex

Structure and chromosomal localization of the human antidiuretic hormone receptor gene

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

Structural determinants of water permeation through aquaporin-1

Control of the selectivity of the aquaporin water channel family by global orientational tuning

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

Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus

Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure

Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion

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195-202

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scholarly article

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10.1093/CKJ/SFS029

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3

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5

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Daniel-G. Bichet

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2012-03-28T00:00:00Z

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270796347

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26069764

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4400507

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