The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.
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Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770Pulmonary epithelial barrier function: some new players and mechanismsHyperacidification of cellubrevin endocytic compartments and defective endosomal recycling in cystic fibrosis respiratory epithelial cellsMultidrug resistance-like genes of Arabidopsis required for auxin transport and auxin-mediated developmentCl- interference with the epithelial Na+ channel ENaCLung infections associated with cystic fibrosis.Immunolocalization and regulation of cystic fibrosis transmembrane conductance regulator in the adult rat epididymis.Understanding the molecular basis of the interaction between NDPK-A and AMPK alpha 1The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular Cl- concentrationElectrophysiological evidence for the presence of cystic fibrosis transmembrane conductance regulator (CFTR) in mouse sperm.Molecular basis for defective glycosylation and Pseudomonas pathogenesis in cystic fibrosis lung.Cystic fibrosis transmembrane conductance regulator and the outwardly rectifying chloride channel: a relationship between two chloride channels expressed in epithelial cells.Regulation of male fertility by CFTR and implications in male infertility.Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channelsInterregulation of proton-gated Na(+) channel 3 and cystic fibrosis transmembrane conductance regulator.Flow cytometry analysis reveals a decrease in intracellular sodium during sperm capacitation.Defective regulatory volume decrease in human cystic fibrosis tracheal cells because of altered regulation of intermediate conductance Ca2+-dependent potassium channelsStatus of fluid and electrolyte absorption in cystic fibrosis.Assessing the Disease-Liability of Mutations in CFTRMutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators.Regulation of the epithelial Na+ channel and airway surface liquid volume by serine proteases.Proteases, cystic fibrosis and the epithelial sodium channel (ENaC).Does epithelial sodium channel hyperactivity contribute to cystic fibrosis lung disease?Ion channels in the endometrium: regulation of endometrial receptivity and embryo implantation.Cystic fibrosis transmembrane conductance regulator modulates neurosecretory function in pulmonary neuroendocrine cell-related tumor cell line models.Activation of large conductance sodium channels upon expression of amiloride-sensitive sodium channel in Sf9 insect cells.Introduction to section IV: biophysical methods to approach CFTR structure.Genistein restores functional interactions between Delta F508-CFTR and ENaC in Xenopus oocytes.Genistein improves regulatory interactions between G551D-cystic fibrosis transmembrane conductance regulator and the epithelial sodium channel in Xenopus oocytes.Synergistic effects of cystic fibrosis transmembrane conductance regulator and aquaporin-9 in the rat epididymis.The effect of ambroxol on chloride transport, CFTR and ENaC in cystic fibrosis airway epithelial cells.Evidence for up-regulation of the endogenous Na-K-2Cl co-transporter by molecular interactions with the anion exchanger tAE1 expressed in Xenopus oocyte.Sodium and epithelial sodium channels participate in the regulation of the capacitation-associated hyperpolarization in mouse sperm.Aquaporin 3 cloned from Xenopus laevis is regulated by the cystic fibrosis transmembrane conductance regulator.Epithelial sodium channels regulate cystic fibrosis transmembrane conductance regulator chloride channels in Xenopus oocytes.Regulatory interactions of N1303K-CFTR and ENaC in Xenopus oocytes: evidence that chloride transport is not necessary for inhibition of ENaC.Abnormal regulatory interactions of I148T-CFTR and the epithelial Na+ channel in Xenopus oocytes.CFTR fails to inhibit the epithelial sodium channel ENaC expressed in Xenopus laevis oocytes.
P2860
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P2860
The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
The first-nucleotide binding d ...... of the epithelial Na+ channel.
@ast
The first-nucleotide binding d ...... of the epithelial Na+ channel.
@en
type
label
The first-nucleotide binding d ...... of the epithelial Na+ channel.
@ast
The first-nucleotide binding d ...... of the epithelial Na+ channel.
@en
prefLabel
The first-nucleotide binding d ...... of the epithelial Na+ channel.
@ast
The first-nucleotide binding d ...... of the epithelial Na+ channel.
@en
P2093
P2860
P356
P1476
The first-nucleotide binding d ...... of the epithelial Na+ channel
@en
P2093
P2860
P304
P356
10.1073/PNAS.96.9.5310
P407
P577
1999-04-01T00:00:00Z