A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
about
Metabolon disruption: a mechanism that regulates bicarbonate transportFunctional analysis of nonsynonymous single nucleotide polymorphisms in human SLC26A9SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epitheliaSLC26A9 is a Cl(-) channel regulated by the WNK kinasesAcute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytesCoupling modes and stoichiometry of Cl-/HCO3- exchange by slc26a3 and slc26a6Epithelial Anion Transport as Modulator of Chemokine SignalingNovel Roles for Chloride Channels, Exchangers, and Regulators in Chronic Inflammatory Airway DiseasesSTAS domain structure and functionMolecular mechanism of pancreatic and salivary gland fluid and HCO3 secretionPhysiology and pathophysiology of bicarbonate secretion by pancreatic duct epitheliumCritical role of bicarbonate and bicarbonate transporters in cardiac functionSLC26A6 and SLC26A7 anion exchangers have a distinct distribution in human kidneyA synthetic chloride channel relaxes airway smooth muscle of the ratIRBIT coordinates epithelial fluid and HCO3- secretion by stimulating the transporters pNBC1 and CFTR in the murine pancreatic ductRegulation of anion exchanger Slc26a6 by protein kinase CDeletion of Slc26a6 alters the stoichiometry of apical Cl-/HCO-3 exchange in mouse pancreatic ductBestrophin Cl- channels are highly permeable to HCO3-Dynamic control of cystic fibrosis transmembrane conductance regulator Cl(-)/HCO3(-) selectivity by external Cl(-)The divergence, actions, roles, and relatives of sodium-coupled bicarbonate transportersInteraction between CFTR and prestin (SLC26A5)The solute carrier 26 family of proteins in epithelial ion transport.The role of the STAS domain in the function and biogenesis of a sulfate transporter as probed by random mutagenesis.Mechanism and synergism in epithelial fluid and electrolyte secretion.Determinants of coupled transport and uncoupled current by the electrogenic SLC26 transporters.The SLC4 family of bicarbonate (HCO₃⁻) transporters.Purinergic regulation of duodenal surface pH and ATP concentration: implications for mucosal defence, lipid uptake and cystic fibrosisCFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.Renal vacuolar H+-ATPase.Open chromatin mapping identifies transcriptional networks regulating human epididymis epithelial function.Native and recombinant Slc26a3 (downregulated in adenoma, Dra) do not exhibit properties of 2Cl-/1HCO3- exchangeCorticosteroids correct aberrant CFTR localization in the duct and regenerate acinar cells in autoimmune pancreatitis.Reciprocal regulation of the primary sodium absorptive pathways in rat intestinal epithelial cells.Regulation of intestinal Cl-/HCO3- exchanger SLC26A3 by intracellular pH.Slc26a6 regulates CFTR activity in vivo to determine pancreatic duct HCO3- secretion: relevance to cystic fibrosisSodium-bicarbonate cotransporter NBCn1/Slc4a7 inhibits NH4Cl-mediated inward current in Xenopus oocytes.SLC26 anion exchangers of guinea pig pancreatic duct: molecular cloning and functional characterization.Composition of mineralizing incisor enamel in cystic fibrosis transmembrane conductance regulator-deficient mice.Value of genetic testing in the management of pancreatitisBicarbonate exchangers SLC26A3 and SLC26A6 are localized at the apical membrane of porcine vas deferens epithelium
P2860
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P2860
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
description
2002 nî lūn-bûn
@nan
2002 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
A molecular mechanism for aberrant CFTR-dependent HCO
@nl
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
@ast
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
@en
type
label
A molecular mechanism for aberrant CFTR-dependent HCO
@nl
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
@ast
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
@en
prefLabel
A molecular mechanism for aberrant CFTR-dependent HCO
@nl
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
@ast
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
@en
P2093
P2860
P356
P1433
P1476
A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.
@en
P2093
Joo Young Choi
Joo Young Kim
Kenichi Ishibashi
Kyung Hwan Kim
Nikolay Shcheynikov
Philip J Thomas
Satoru Naruse
Shigeru B H Ko
Shmuel Muallem
P2860
P304
P356
10.1093/EMBOJ/CDF580
P407
P50
P577
2002-11-01T00:00:00Z