Regulation of CFTR expression and function during differentiation of intestinal epithelial cells.
about
The multidrug resistance and cystic fibrosis genes have complementary patterns of epithelial expression.Cell-type-specific long-range looping interactions identify distant regulatory elements of the CFTR geneThe mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.CFTR and differentiation markers expression in non-CF and delta F 508 homozygous CF nasal epithelium.CFTR: covalent modification of cysteine-substituted channels expressed in Xenopus oocytes shows that activation is due to the opening of channels resident in the plasma membraneCell culture models demonstrate that CFTR dysfunction leads to defective fatty acid composition and metabolismNa-K-2Cl cotransporter gene expression and function during enterocyte differentiation. Modulation of Cl- secretory capacity by butyrateDirected differentiation of human pluripotent stem cells into mature airway epithelia expressing functional CFTR protein.Cytokine-Regulation of Na+-K+-Cl- Cotransporter 1 and Cystic Fibrosis Transmembrane Conductance Regulator-Potential Role in Pulmonary Inflammation and Edema Formation.A dicistronic construct allows easy detection of human CFTR expression from YAC DNA in human cells.Tetramethylpyrazine stimulates cystic fibrosis transmembrane conductance regulator-mediated anion secretion in distal colon of rodents.Differential Cl- and HCO3- mediated anion secretion by different colonic cell types in response to tetromethylpyrazine.Conformational maturation of CFTR but not its mutant counterpart (delta F508) occurs in the endoplasmic reticulum and requires ATPFunctional expression and apical localization of the cystic fibrosis transmembrane conductance regulator in MDCK I cells.Cyclic AMP-induced mucin exocytosis is independent of Cl- movements in human colonic epithelial cells (HT29-Cl.16E).Recent Progress in CFTR Interactome Mapping and Its Importance for Cystic Fibrosis.SLC6A14, an amino acid transporter, modifies the primary CF defect in fluid secretionProlonged co-treatment with HGF sustains epithelial integrity and improves pharmacological rescue of Phe508del-CFTR
P2860
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P2860
Regulation of CFTR expression and function during differentiation of intestinal epithelial cells.
description
1992 nî lūn-bûn
@nan
1992 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年学术文章
@wuu
1992年学术文章
@zh-cn
1992年学术文章
@zh-hans
1992年学术文章
@zh-my
1992年学术文章
@zh-sg
1992年學術文章
@yue
name
Regulation of CFTR expression ...... f intestinal epithelial cells.
@ast
Regulation of CFTR expression ...... f intestinal epithelial cells.
@en
type
label
Regulation of CFTR expression ...... f intestinal epithelial cells.
@ast
Regulation of CFTR expression ...... f intestinal epithelial cells.
@en
prefLabel
Regulation of CFTR expression ...... f intestinal epithelial cells.
@ast
Regulation of CFTR expression ...... f intestinal epithelial cells.
@en
P2093
P2860
P1433
P1476
Regulation of CFTR expression ...... f intestinal epithelial cells.
@en
P2093
Auerbach W
Buchwald M
Riordan JR
P2860
P304
P407
P577
1992-07-01T00:00:00Z