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.
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Pharmacological chaperoning: a primer on mechanism and pharmacologyAltered agonist sensitivity of a mutant v2 receptor suggests a novel therapeutic strategy for nephrogenic diabetes insipidus.Biased signaling favoring gi over β-arrestin promoted by an apelin fragment lacking the C-terminal phenylalanineOxytocin and vasopressin agonists and antagonists as research tools and potential therapeutics.The μ-opioid receptor variant N190K is unresponsive to peptide agonists yet can be rescued by small-molecule drugs.Enhanced BRET Technology for the Monitoring of Agonist-Induced and Agonist-Independent Interactions between GPCRs and β-ArrestinsSignaling Modification by GPCR Heteromer and Its Implication on X-Linked Nephrogenic Diabetes Insipidus.Identification and characterization of an activating F229V substitution in the V2 vasopressin receptor in an infant with NSIAD.Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.Functional polymorphisms affecting the clinically important arginine-137 residue of AVPR2 do not influence serum sodium concentration at the population levelMutations of Vasopressin Receptor 2 Including Novel L312S Have Differential Effects on Trafficking.Familial forms of diabetes insipidus: clinical and molecular characteristics.Nephrogenic syndrome of inappropriate antidiuresis secondary to an activating mutation in the arginine vasopressin receptor AVPR2.V2 vasopressin receptor (V2R) mutations in partial nephrogenic diabetes insipidus highlight protean agonism of V2R antagonists.Characterization of three vasopressin receptor 2 variants: an apparent polymorphism (V266A) and two loss-of-function mutations (R181C and M311V)Genetic variants affecting equivalent protein family positions reflect human diversity.Lack of responsiveness to 1-desamino-D arginin vasopressin (desmopressin) in male patients with nephrogenic syndrome of inappropriate antidiuresis: from bench to bedside.Hereditary Nephrogenic Diabetes Insipidus: Pathophysiology and Possible Treatment. An Update.GPCR Retreat 2012: timing is everything.
P2860
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P2860
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.
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Functional characterization of ...... : implications for treatments.
@ast
Functional characterization of ...... : implications for treatments.
@en
type
label
Functional characterization of ...... : implications for treatments.
@ast
Functional characterization of ...... : implications for treatments.
@en
prefLabel
Functional characterization of ...... : implications for treatments.
@ast
Functional characterization of ...... : implications for treatments.
@en
P2093
P2860
P356
P1476
Functional characterization of ...... : implications for treatments.
@en
P2093
Abraham Kovoor
Eric Carpentier
Gabriel A Vargas
Geneviève Oligny-Longpré
Moulay D Rochdi
Stanford Chen
Stephen E Gitelman
Stephen M Rosenthal
P2860
P304
P356
10.1124/MOL.109.061804
P577
2010-02-16T00:00:00Z