about
The Trafficking of the Water Channel Aquaporin-2 in Renal Principal Cells-a Potential Target for Pharmacological Intervention in Cardiovascular DiseasesOsmotic homeostasisPharmacoperones: a new therapeutic approach for diseases caused by misfolded G protein-coupled receptorsInvolvement of the V2 vasopressin receptor in adaptation to limited water supplyA large deletion of the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family.Excess maternal salt intake produces sex-specific hypertension in offspring: putative roles for kidney and gastrointestinal sodium handlingNephrogenic diabetes insipidus in mice caused by deleting COOH-terminal tail of aquaporin-2.Trafficking of G-protein-coupled receptors to the plasma membrane: insights for pharmacoperone drugs.Characterization of D150E and G196D aquaporin-2 mutations responsible for nephrogenic diabetes insipidus: importance of a mild phenotype.Functional characterization of vasopressin type 2 receptor substitutions (R137H/C/L) leading to nephrogenic diabetes insipidus and nephrogenic syndrome of inappropriate antidiuresis: implications for treatments.High-throughput chemical screening identifies AG-490 as a stimulator of aquaporin 2 membrane expression and urine concentrationClinical overview of nephrogenic diabetes insipidus based on a nationwide survey in Japan.Congenital progressive hydronephrosis (cph) is caused by an S256L mutation in aquaporin-2 that affects its phosphorylation and apical membrane accumulation.Novel mutation in the AVPR2 gene in a Danish male with nephrogenic diabetes insipidus caused by ER retention and subsequent lysosomal degradation of the mutant receptor.Pharmacological chaperones for misfolded gonadotropin-releasing hormone receptorsNovel compound aquaporin 2 mutations in nephrogenic diabetes insipidusNovel autosomal recessive gene mutations in aquaporin-2 in two Chinese congenital nephrogenic diabetes insipidus pedigrees.Evolutionary Influenced Interaction Pattern as Indicator for the Investigation of Natural Variants Causing Nephrogenic Diabetes Insipidus.A Rare Case of Congenital Diabetes Insipidus.Diagnosis of diabetes insipidus observed in Swiss Duroc boarsNephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.Soluble (pro)renin receptor via β-catenin enhances urine concentration capability as a target of liver X receptor.Conivaptan: a step forward in the treatment of hyponatremia?Lithium-induced nephrogenic diabetes insipidus: renal effects of amiloride.Mouse models and the urinary concentrating mechanism in the new millennium.Defective Store-Operated Calcium Entry Causes Partial Nephrogenic Diabetes InsipidusHsp90 inhibitor partially corrects nephrogenic diabetes insipidus in a conditional knock-in mouse model of aquaporin-2 mutation.Localization and trafficking of aquaporin 2 in the kidney.A novel v2 vasopressin receptor mutation with x-linked nephrogenic diabetes insipidusMechanisms of cell polarity and aquaporin sorting in the nephron.Inherited secondary nephrogenic diabetes insipidus: concentrating on humans.Molecular physiology of the medullary collecting duct.Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus.Development and Diseases of the Collecting Duct System.Mutations in the AVPR2, AVP-NPII, and AQP2 genes in Turkish patients with diabetes insipidus.A novel mutation in AVPR2 causing congenital nephrogenic diabetes insipidus with complete resistance to antidiuretic hormone.A de novo novel missense mutation in AVPR2 with severe nephrogenic diabetes insipidus.Nephrogenic diabetes insipidus (NDI): clinical, laboratory and genetic characterization of five Brazilian patients.A novel AVPR2 gene mutation of X-linked congenital nephrogenic diabetes insipidus in an Asian pedigreePemetrexed-Induced Nephrogenic Diabetes Insipidus.
P2860
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P2860
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
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Molecular biology of hereditary diabetes insipidus.
@ast
Molecular biology of hereditary diabetes insipidus.
@en
Molecular biology of hereditary diabetes insipidus.
@nl
type
label
Molecular biology of hereditary diabetes insipidus.
@ast
Molecular biology of hereditary diabetes insipidus.
@en
Molecular biology of hereditary diabetes insipidus.
@nl
prefLabel
Molecular biology of hereditary diabetes insipidus.
@ast
Molecular biology of hereditary diabetes insipidus.
@en
Molecular biology of hereditary diabetes insipidus.
@nl
P356
P1476
Molecular biology of hereditary diabetes insipidus
@en
P2093
T Mary Fujiwara
P304
P356
10.1681/ASN.2005040371
P577
2005-08-10T00:00:00Z