Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation.
about
Expression of a renal type I sodium/phosphate transporter (NaPi-1) induces a conductance in Xenopus oocytes permeable for organic and inorganic anionsCase studies in cholera: lessons in medical history and science.Flufenamic acid as an ion channel modulator.Phosphate stimulates CFTR Cl- channelsBiochemical status of renal epithelial Na+ channels determines apparent channel conductance, ion selectivity, and amiloride sensitivity.Effect of ATP concentration on CFTR Cl- channels: a kinetic analysis of channel regulationLocalization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization.Defective fluid transport by cystic fibrosis airway epithelia.The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.The interaction of gut microbes with host ABC transporters.The cystic fibrosis transmembrane conductance regulator gene.Comparative genomic sequence analysis of the human and mouse cystic fibrosis transmembrane conductance regulator genes.Cell and gene therapy for genetic diseases: inherited disorders affecting the lung and those mimicking sudden infant death syndromeEfficient expression of CFTR function with adeno-associated virus vectors that carry shortened CFTR genes.Functionally distinct phospho-forms underlie incremental activation of protein kinase-regulated Cl- conductance in mammalian heart.ATP dependence of Na+/H+ exchange. Nucleotide specificity and assessment of the role of phospholipidsPermeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions.Status of fluid and electrolyte absorption in cystic fibrosis.Functional characterization of novel ABCB6 mutations and their clinical implications in familial pseudohyperkalemiaRepeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosisMechanism of dysfunction of two nucleotide binding domain mutations in cystic fibrosis transmembrane conductance regulator that are associated with pancreatic sufficiency.ABC proteins protect the human body and maintain optimal health.Research on cystic fibrosis: a journey from the Heart House.EG-VEGF, BV8, and their receptor expression in human bronchi and their modification in cystic fibrosis: Impact of CFTR mutation (delF508).Gene therapy for the respiratory manifestations of cystic fibrosis.Sequence homologies between nucleotide binding regions of CFTR and G-proteins suggest structural and functional similarities.Cystic fibrosis transmembrane conductance regulator mediates sulphonylurea block of the inwardly rectifying K+ channel Kir6.1.CFTR Cl- channel and CFTR-associated ATP channel: distinct pores regulated by common gates.Alternate stimulation of apical CFTR by genistein in epithelia.Effects of lovastatin on trafficking of cystic fibrosis transmembrane conductance regulator in human tracheal epithelium.Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels.Differential expression of ORCC and CFTR induced by low temperature in CF airway epithelial cells.Induction of multidrug resistance downregulates the expression of CFTR in colon epithelial cells.The cystic fibrosis mutation (delta F508) does not influence the chloride channel activity of CFTR.Nucleotide occlusion in the human cystic fibrosis transmembrane conductance regulator. Different patterns in the two nucleotide binding domains.Alternate translation initiation codons can create functional forms of cystic fibrosis transmembrane conductance regulator.Phorbol ester activation of chloride current in guinea-pig ventricular myocytes.Cystic fibrosis genotypes and views on screening are both heterogeneous and population related.Deactivation of CFTR-Cl conductance by endogenous phosphatases in the native sweat duct.Characterization of cyclic AMP-regulated chloride conductance in the pigmented rabbit conjunctival epithelial cells.
P2860
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P2860
Cystic fibrosis transmembrane conductance regulator: a chloride channel with novel regulation.
description
1992 nî lūn-bûn
@nan
1992 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի մայիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Cystic fibrosis transmembrane ...... channel with novel regulation.
@ast
Cystic fibrosis transmembrane ...... channel with novel regulation.
@en
type
label
Cystic fibrosis transmembrane ...... channel with novel regulation.
@ast
Cystic fibrosis transmembrane ...... channel with novel regulation.
@en
prefLabel
Cystic fibrosis transmembrane ...... channel with novel regulation.
@ast
Cystic fibrosis transmembrane ...... channel with novel regulation.
@en
P2093
P1433
P1476
Cystic fibrosis transmembrane ...... channel with novel regulation.
@en
P2093
Anderson MP
Denning GM
Gregory RJ
Ostedgaard LS
Sheppard DN
P304
P356
10.1016/0896-6273(92)90196-K
P407
P577
1992-05-01T00:00:00Z