Cystic fibrosis transmembrane conductance regulator. Structure and function of an epithelial chloride channel.
about
Mechanisms of the noxious inflammatory cycle in cystic fibrosisHematopoietic and mesenchymal stem cells for the treatment of chronic respiratory diseases: role of plasticity and heterogeneityStructural basis of the Na+/H+ exchanger regulatory factor PDZ1 interaction with the carboxyl-terminal region of the cystic fibrosis transmembrane conductance regulatorThe elements of life and medicinesAdditive effect of multiple pharmacological chaperones on maturation of CFTR processing mutants4'-Methyl-4,5'-bithiazole-based correctors of defective delta F508-CFTR cellular processing.Regulation of volume-activated chloride channels by P-glycoprotein: phosphorylation has the final say!Binding and Selectivity of Halides with Macrocyclic polyamines.Experimental and theoretical studies on halide binding with a p-xylyl-based azamacrocycle.Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect.The phenotypic consequences of CFTR mutations.Small molecule inhibition of the Na(+)/H(+) exchange regulatory factor 1 and parathyroid hormone 1 receptor interaction.Divergent CFTR orthologs respond differently to the channel inhibitors CFTRinh-172, glibenclamide, and GlyH-101ATP release via anion channels.Regulation of calcium-activated chloride channels in smooth muscle cells: a complex picture is emerging.Animal Enterotoxigenic Escherichia coli.Stem cell therapy for cystic fibrosis: current status and future prospects.Golgi bypass: skirting around the heart of classical secretion.The application of Ussing chambers for determining the impact of microbes and probiotics on intestinal ion transport.Functional architecture of the CFTR chloride channel.The plant multidrug resistance ABC transporter AtMRP5 is involved in guard cell hormonal signalling and water use.Control of cellular GADD34 levels by the 26S proteasome.Processing mutations located throughout the human multidrug resistance P-glycoprotein disrupt interactions between the nucleotide binding domains.Binding of sulfonylurea by AtMRP5, an Arabidopsis multidrug resistance-related protein that functions in salt tolerance.Introduction of the most common cystic fibrosis mutation (Delta F508) into human P-glycoprotein disrupts packing of the transmembrane segments.Localization of sequences within the C-terminal domain of the cystic fibrosis transmembrane conductance regulator which impact maturation and stability.Hematopoietic stem/progenitor cells express functional mitochondrial energy-dependent cystic fibrosis transmembrane conductance regulator.Increased Expression of Plasma-Induced ABCC1 mRNA in Cystic Fibrosis.Cystic fibrosis transmembrane conductance regulator: the NBF1+R (nucleotide-binding fold 1 and regulatory domain) segment acting alone catalyses a Co2+/Mn2+/Mg2+-ATPase activity markedly inhibited by both Cd2+ and the transition-state analogue orthoAnalysis of c.3499+200TA(7_56) and D7S523 Microsatellites Linked to Cystic Fibrosis Transmembrane Regulator.Molecular dynamics simulation of the transmembrane subunit of BtuCD in the lipid bilayer.Identification of a region of strong discrimination in the pore of CFTR.Disassembly and degradation of photosystem I in an in vitro system are multievent, metal-dependent processes.Purification and crystallization of the cystic fibrosis transmembrane conductance regulator (CFTR).Destabilization of the transmembrane domain induces misfolding in a phenotypic mutant of cystic fibrosis transmembrane conductance regulator.The distribution of Abcc6 in normal mouse tissues suggests multiple functions for this ABC transporter.CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes.Use of a 4-week up-titration regimen of roflumilast in patients with severe COPD.Topology studies of the chloroplast protein import channel Toc75.Revisiting sweat chloride test results based on recent guidelines for diagnosis of cystic fibrosis.
P2860
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P2860
Cystic fibrosis transmembrane conductance regulator. Structure and function of an epithelial chloride channel.
description
2000 nî lūn-bûn
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2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Cystic fibrosis transmembrane ...... n epithelial chloride channel.
@ast
Cystic fibrosis transmembrane ...... n epithelial chloride channel.
@en
type
label
Cystic fibrosis transmembrane ...... n epithelial chloride channel.
@ast
Cystic fibrosis transmembrane ...... n epithelial chloride channel.
@en
prefLabel
Cystic fibrosis transmembrane ...... n epithelial chloride channel.
@ast
Cystic fibrosis transmembrane ...... n epithelial chloride channel.
@en
P2860
P356
P1476
Cystic fibrosis transmembrane ...... n epithelial chloride channel.
@en
P2093
P2860
P304
P356
10.1074/JBC.275.6.3729
P407
P577
2000-02-01T00:00:00Z