about
Early pulmonary inflammation and lung damage in children with cystic fibrosisMitochondrial cAMP signalingRegulation of ion channels and transporters by AMP-activated kinase (AMPK).Abnormal n-6 fatty acid metabolism in cystic fibrosis is caused by activation of AMP-activated protein kinaseCellular distribution and function of ion channels involved in transport processes in rat tracheal epithelium.Abnormal unsaturated fatty acid metabolism in cystic fibrosis: biochemical mechanisms and clinical implications.Hydrogen peroxide stimulation of CFTR reveals an Epac-mediated, soluble AC-dependent cAMP amplification pathway common to GPCR signallingPharmGKB summary: very important pharmacogene information for CFTRPhosphoproteomic analysis of the highly-metastatic hepatocellular carcinoma cell line, MHCC97-HTgf-beta downregulation of distinct chloride channels in cystic fibrosis-affected epithelia.Using Drugs to Probe the Variability of Trans-Epithelial Airway Resistance."Store-operated" cAMP signaling contributes to Ca2+-activated Cl- secretion in T84 colonic cellsCFTR Knockdown induces proinflammatory changes in intestinal epithelial cells.Calcium-ATPases: Gene disorders and dysregulation in cancer.Synergy of cAMP and calcium signaling pathways in CFTR regulation.The secret life of CFTR as a calcium-activated chloride channel.Nucleoside diphosphate kinases (NDPKs) in animal development.Repairing the basic defect in cystic fibrosis - one approach is not enough.Insulin signaling via the PI3-kinase/Akt pathway regulates airway glucose uptake and barrier function in a CFTR-dependent manner.Hydrogen sulfide stimulates CFTR in Xenopus oocytes by activation of the cAMP/PKA signalling axisAnoctamin 1 (Ano1) is required for glucose-induced membrane potential oscillations and insulin secretion by murine β-cells.New Insights into the Molecular Mechanisms Targeting Tubular Channels/Transporters in PKD Development.Mutations of Cystic Fibrosis Transmembrane Conductance Regulator Gene Cause a Monocyte-Selective Adhesion Deficiency.Localization of cystic fibrosis transmembrane conductance regulator signaling complexes in human salivary gland striated duct cells.Airway surface liquid pH is not acidic in children with cystic fibrosis.NM23 proteins: innocent bystanders or local energy boosters for CFTR?A role for the cystic fibrosis transmembrane conductance regulator in the nitric oxide-dependent release of Cl- from acidic organelles in amacrine cells.CFTR mutation enhances Dishevelled degradation and results in impairment of Wnt-dependent hematopoiesis.Functional roles of glutamic acid E143 and E705 residues in the N-terminus and transmembrane domain 7 of Anoctamin 1 in calcium and noxious heat sensing.Calcium-induced chloride secretion is decreased by Resveratrol in ileal porcine tissue
P2860
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P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@ast
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@en
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@nl
type
label
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@ast
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@en
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@nl
prefLabel
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@ast
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@en
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@nl
P2860
P3181
P356
P1433
P1476
CFTR: a hub for kinases and crosstalk of cAMP and Ca2+
@en
P2093
Anil Mehta
P2860
P304
P3181
P356
10.1111/FEBS.12457
P407
P577
2013-08-27T00:00:00Z