Identification of transport abnormalities in duodenal mucosa and duodenal enterocytes from patients with cystic fibrosis.
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Acute regulation of the SLC26A3 congenital chloride diarrhoea anion exchanger (DRA) expressed in Xenopus oocytesCellular bicarbonate protects rat duodenal mucosa from acid-induced injuryLung infections associated with cystic fibrosis.Defective goblet cell exocytosis contributes to murine cystic fibrosis-associated intestinal disease.Effect of E. coli heat-stable enterotoxin on colonic transport in guanylyl cyclase C receptor-deficient mice.Impact of CFTR Modulation on Intestinal pH, Motility, and Clinical Outcomes in Patients With Cystic Fibrosis and the G551D Mutation.Clinical and pharmacological experience with LJP-394.Functional vacuolar ATPase (V-ATPase) proton pumps traffic to the enterocyte brush border membrane and require CFTR.Pharmacological treatment of the ion transport defect in cystic fibrosis.Efficacy and safety of a unique enteric-coated bicarbonate-buffered pancreatic enzyme replacement therapy in children and adults with cystic fibrosis.Measurements of CFTR-mediated Cl- secretion in human rectal biopsies constitute a robust biomarker for Cystic Fibrosis diagnosis and prognosis.Electrolyte transport in the mammalian colon: mechanisms and implications for disease.Molecular mechanisms of calcium-sensing receptor-mediated calcium signaling in the modulation of epithelial ion transport and bicarbonate secretionCFTR and bicarbonate secretion by [correction of to] epithelial cells.Stimulation of Airway and Intestinal Mucosal Secretion by Natural Coumarin CFTR ActivatorsMyosin Ia is required for CFTR brush border membrane trafficking and ion transport in the mouse small intestine.Gender-specific protection of estrogen against gastric acid-induced duodenal injury: stimulation of duodenal mucosal bicarbonate secretion.Regulated traffic of anion transporters in mammalian Brunner's glands: a role for water and fluid transport.Role of down-regulated in adenoma anion exchanger in HCO3- secretion across murine duodenum.Normal mouse intestinal mucus release requires cystic fibrosis transmembrane regulator-dependent bicarbonate secretion.Infectious diarrhea: Cellular and molecular mechanisms.New advances in the pathophysiology of intestinal ion transport and barrier function in diarrhea and the impact on therapy.Molecular motors and apical CFTR traffic in epithelia.Expression of a wild-type CFTR maintains the integrity of the biosynthetic/secretory pathway in human cystic fibrosis pancreatic duct cells.Choosing sides in the battle against gastric acid.Mechanism of augmented duodenal HCO(3)(-) secretion after elevation of luminal CO(2).Chloride conductance of CFTR facilitates basal Cl-/HCO3- exchange in the villous epithelium of intact murine duodenum.PAT-1 (Slc26a6) is the predominant apical membrane Cl-/HCO3- exchanger in the upper villous epithelium of the murine duodenum.A new role for bicarbonate secretion in cervico-uterine mucus release.Human duodenal spheroids for noninvasive intracellular pH measurement and quantification of regulation mechanisms under physiological conditions.Dehydrocostuslactone, a sesquiterpene lactone activates wild-type and ΔF508 mutant CFTR chloride channel.Quantitative assessment of motility-associated changes in gastric and duodenal luminal pH in humans.Protein kinase C potentiates cAMP-stimulated mouse duodenal mucosal bicarbonate secretion in vitro.Lateral intercellular space volume as a determinant of CFTR-mediated anion secretion across small intestinal mucosa.Small intestinal glucose absorption in cystic fibrosis: a study in human and transgenic DeltaF508 cystic fibrosis mouse tissues.Fat absorption in cystic fibrosis mice is impeded by defective lipolysis and post-lipolytic events.AP2 α modulates cystic fibrosis transmembrane conductance regulator function in the human intestine.
P2860
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P2860
Identification of transport abnormalities in duodenal mucosa and duodenal enterocytes from patients with cystic fibrosis.
description
2000 nî lūn-bûn
@nan
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
2000年论文
@zh
2000年论文
@zh-cn
name
Identification of transport ab ...... patients with cystic fibrosis.
@en
type
label
Identification of transport ab ...... patients with cystic fibrosis.
@en
prefLabel
Identification of transport ab ...... patients with cystic fibrosis.
@en
P2093
P1433
P1476
Identification of transport ab ...... patients with cystic fibrosis.
@en
P2093
B A Martensson
J I Isenberg
V S Pratha
P304
P356
10.1016/S0016-5085(00)70358-1
P407
P577
2000-06-01T00:00:00Z