Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization.
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Dab2 is a key regulator of endocytosis and post-endocytic trafficking of the cystic fibrosis transmembrane conductance regulatorDistribution of aquaporin water channels AQP1 and AQP5 in the ductal system of the human pancreasWNK4 regulates apical and basolateral Cl- flux in extrarenal epitheliaDistribution of ClC-2 chloride channel in rat and human epithelial tissuesDisruption of the K+ channel beta-subunit KCNE3 reveals an important role in intestinal and tracheal Cl- transportCell-specific expression of epithelial sodium channel alpha, beta, and gamma subunits in aldosterone-responsive epithelia from the rat: localization by in situ hybridization and immunocytochemistryCellular bicarbonate protects rat duodenal mucosa from acid-induced injurySTa and cGMP stimulate CFTR translocation to the surface of villus enterocytes in rat jejunum and is regulated by protein kinase GEnteric bacterial toxins: mechanisms of action and linkage to intestinal secretion.Functional Cftr in crypt epithelium of organotypic enteroid cultures from murine small intestineDifferential roles of NHERF1, NHERF2, and PDZK1 in regulating CFTR-mediated intestinal anion secretion in mice.CFTR chloride channel as a molecular target of anthraquinone compounds in herbal laxativesTissue and cellular expression patterns of porcine CFTR: similarities to and differences from human CFTRA host defense mechanism involving CFTR-mediated bicarbonate secretion in bacterial prostatitis.DeltaF508 CFTR protein expression in tissues from patients with cystic fibrosis.Salmonella enterica serovar typhi modulates cell surface expression of its receptor, the cystic fibrosis transmembrane conductance regulator, on the intestinal epithelium.WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epithelia.Electrolyte transport in the mammalian colon: mechanisms and implications for disease.The mitochondrial complex I activity is reduced in cells with impaired cystic fibrosis transmembrane conductance regulator (CFTR) function.Physiological relevance of cell-specific distribution patterns of CFTR, NKCC1, NBCe1, and NHE3 along the crypt-villus axis in the intestine.Abnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect.Animal models of gastrointestinal and liver diseases. Animal models of cystic fibrosis: gastrointestinal, pancreatic, and hepatobiliary disease and pathophysiology.Cystic fibrosis: an inherited disease affecting mucin-producing organs.Nucleosome occupancy reveals regulatory elements of the CFTR promoter.A mouse model for the delta F508 allele of cystic fibrosis.Increased levels of anti-glycan antibodies in patients with cystic fibrosis.Cyclic AMP-induced K+ secretion occurs independently of Cl- secretion in rat distal colonCFTR, mucins, and mucus obstruction in cystic fibrosis.Chloride channel diseases resulting from impaired transepithelial transport or vesicular functionCFTR Knockdown induces proinflammatory changes in intestinal epithelial cells.Pancreatic and biliary secretion are both altered in cystic fibrosis pigs.In vivo analysis of DNase I hypersensitive sites in the human CFTR gene.Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.Regulated traffic of anion transporters in mammalian Brunner's glands: a role for water and fluid transport.The cystic fibrosis intestine.Characterization of CFTR High Expresser cells in the intestine.Expression of Cystic Fibrosis Transmembrane Conductance Regulator in Ganglia of Human Gastrointestinal TractCholera toxin disrupts barrier function by inhibiting exocyst-mediated trafficking of host proteins to intestinal cell junctionsPlasma membrane glutathione transporters and their roles in cell physiology and pathophysiologyNa-K-2Cl cotransporter gene expression and function during enterocyte differentiation. Modulation of Cl- secretory capacity by butyrate
P2860
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P2860
Localization of cystic fibrosis transmembrane conductance regulator mRNA in the human gastrointestinal tract by in situ hybridization.
description
1994 nî lūn-bûn
@nan
1994 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1994 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
name
Localization of cystic fibrosi ...... ract by in situ hybridization.
@ast
Localization of cystic fibrosi ...... ract by in situ hybridization.
@en
Localization of cystic fibrosi ...... ract by in situ hybridization.
@nl
type
label
Localization of cystic fibrosi ...... ract by in situ hybridization.
@ast
Localization of cystic fibrosi ...... ract by in situ hybridization.
@en
Localization of cystic fibrosi ...... ract by in situ hybridization.
@nl
prefLabel
Localization of cystic fibrosi ...... ract by in situ hybridization.
@ast
Localization of cystic fibrosi ...... ract by in situ hybridization.
@en
Localization of cystic fibrosi ...... ract by in situ hybridization.
@nl
P2093
P2860
P356
P1476
Localization of cystic fibrosi ...... ract by in situ hybridization.
@en
P2093
P2860
P304
P356
10.1172/JCI116966
P407
P577
1994-01-01T00:00:00Z