Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct - Wikidata - awgldk - TriplyDB

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

http://www.wikidata.org/entity/Q24607623

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Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin-CD water channels to plasma membrane Clint: a novel clathrin-binding ENTH-domain protein at the Golgi The aquaporin family of molecular water channels Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene Hyponatremia Associated with Heart Failure: Pathological Role of Vasopressin-Dependent Impaired Water Excretion A novel therapeutic effect of statins on nephrogenic diabetes insipidus Molecular cloning and characterization of an aquaporin cDNA from salivary, lacrimal, and respiratory tissues Lithium-induced downregulation of aquaporin-2 water channel expression in rat kidney medulla Localization and functional characterization of rat kidney-specific chloride channel, ClC-K1 A panoramic view of gene expression in the human kidney Three families with autosomal dominant nephrogenic diabetes insipidus caused by aquaporin-2 mutations in the C-terminus.Water channels encoded by mutant aquaporin-2 genes in nephrogenic diabetes insipidus are impaired in their cellular routing.Characterization of growth, glomerular number, and tubular proteins in the developing rhesus monkey kidney.Countercurrent exchange in the renal medulla.Increased urinary excretion of aquaporin 2 in patients with liver cirrhosis Novel compound aquaporin 2 mutations in nephrogenic diabetes insipidus Aquaporins: a promising target for drug development.Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.Congestive heart failure in rats is associated with increased expression and targeting of aquaporin-2 water channel in collecting duct Increased CSF aquaporin-4, and interleukin-6 levels in dogs with idiopathic communicating internal hydrocephalus and a decrease after ventriculo-peritoneal shunting Familial forms of diabetes insipidus: clinical and molecular characteristics.Urinary concentration: different ways to open and close the tap.Dynamic regulation and dysregulation of the water channel aquaporin-2: a common cause of and promising therapeutic target for water balance disorders.Pathophysiology, diagnosis and management of nephrogenic diabetes insipidus.Expression and distribution of aquaporin of collecting duct are regulated by vasopressin V2 receptor in rat kidney.Nephrogenic diabetes insipidus (NDI): clinical, laboratory and genetic characterization of five Brazilian patients.Differential stability of biogenesis intermediates reveals a common pathway for aquaporin-1 topological maturation.Phosphorylation of serine 256 is required for cAMP-dependent regulatory exocytosis of the aquaporin-2 water channel.cAMP-dependent phosphorylation stimulates water permeability of aquaporin-collecting duct water channel protein expressed in Xenopus oocytes.Hypotonicity reduces the activity of murine aquaporin-2 promoter induced by dibutyryl cAMP.Adipocytes support cAMP-dependent translocation of aquaporin-2 from intracellular sites distinct from the insulin-responsive GLUT4 storage compartment.Molecular and functional characterization of a vasotocin-sensitive aquaporin water channel in quail kidney.Single-tubule RNA-Seq uncovers signaling mechanisms that defend against hyponatremia in SIADH.Effect of water deprivation and hypertonic saline infusion on urinary AQP2 excretion in healthy humans.AQP2 is a substrate for endogenous PP2B activity within an inner medullary AKAP-signaling complex.Chronic elevation of IL-1β induces diuresis via a cyclooxygenase 2-mediated mechanism.Hypertonicity regulates the aquaporin-2 promoter independently of arginine vasopressin.The perinatal expression of aquaporin-2 and aquaporin-3 in developing kidney.Urinary excretion of the water channel aquaporin 2 correlated with the pharmacological effect of tolvaptan in cirrhotic patients with ascites.Aquaporins passively transport water into cells

P2860

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P2860

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

http://www.wikidata.org/entity/Q24607623

description

1994 nî lūn-bûn

@nan

1994 թուականի Մարտին հրատարակուած գիտական յօդուած

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1994 թվականի մարտին հրատարակված գիտական հոդված

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1994年の論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年論文

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1994年论文

@wuu

name

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@ast

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@en

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@nl

type

label

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@ast

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@en

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@nl

prefLabel

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@ast

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@en

Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

@nl

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Journal of Clinical Investigation

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Cloning, characterization, and chromosomal mapping of human aquaporin of collecting duct

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P2093

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P2860

Isolation of the cDNA for erythrocyte integral membrane protein of 28 kilodaltons: member of an ancient channel family

Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus

Cleavage of structural proteins during the assembly of the head of bacteriophage T4

Appearance of water channels in Xenopus oocytes expressing red cell CHIP28 protein

Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus

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

Amino acid sequence of in vivo phosphorylation sites in the main intrinsic protein (MIP) of lens membranes

Erythrocyte Mr 28,000 transmembrane protein exists as a multisubunit oligomer similar to channel proteins

Cloning and characterization of a vasopressin V2 receptor and possible link to nephrogenic diabetes insipidus

Identification, purification, and partial characterization of a novel Mr 28,000 integral membrane protein from erythrocytes and renal tubules

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1250-6

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399655

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10.1172/JCI117079

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