Pathogenesis of congenital alkalosis with diarrhea. Implications for the physiology of normal ileal electrolyte absorption and secretion.
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LPA stimulates intestinal DRA gene transcription via LPA2 receptor, PI3K/AKT, and c-Fos-dependent pathwayFunctional analysis of diastrophic dysplasia sulfate transporter. Its involvement in growth regulation of chondrocytes mediated by sulfated proteoglycansAbsorption and secretion by the colon.Jejunal absorption and secretion of calcium in patients with chronic renal disease on hemodialysis.Stimulation of active and passive sodium absorption by sugars in the human jejunum.Effect of dietary calcium and age on jejunal calcium absorption in humans studied by intestinal perfusionCongenital chloride diarrhoea. Clinical analysis of 21 Finnish patientsAbnormal passive chloride absorption in cystic fibrosis jejunum functionally opposes the classic chloride secretory defect.Congenital chloridorrhoeaColonic electrolyte transport in health and in congenital chloride diarrheaJejunal and ileal absorption in patients with chronic renal disease. Effect of 1alpha-hydroxycholecalciferol.Magnesium absorption in the human small intestine. Results in normal subjects, patients with chronic renal disease, and patients with absorptive hypercalciuria.Acid-base transport systems in gastrointestinal epitheliaCaptopril in congenital chloride diarrhoea: a case studyAll-trans-retinoic Acid Increases SLC26A3 DRA (Down-regulated in Adenoma) Expression in Intestinal Epithelial Cells via HNF-1βThe gene for congenital chloride diarrhea maps close to but is distinct from the gene for cystic fibrosis transmembrane conductance regulatorActive chloride secretion in the normal human jejunum.Transcriptional modulation of SLC26A3 (DRA) by sphingosine-1-phosphate.Functional coupling of the downregulated in adenoma Cl-/base exchanger DRA and the apical Na+/H+ exchangers NHE2 and NHE3.The role of intestinal oxalate transport in hyperoxaluria and the formation of kidney stones in animals and man.Acute pre-renal failure: acquired chloride diarrhea after bowel resectionSulfate and chloride transport in Caco-2 cells: differential regulation by thyroxine and the possible role of DRA gene.Electroneutral, HCO3(-)-independent, pH gradient-dependent uphill transport of Cl- by ileal brush-border membrane vesicles. Possible role in the pathogenesis of chloridorrhea.Three distinct mechanisms of HCO3- secretion in rat distal colon.Defective jejunal brush border membrane sodium/proton exchange in association with lethal familial protracted diarrhoea.
P2860
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P2860
Pathogenesis of congenital alkalosis with diarrhea. Implications for the physiology of normal ileal electrolyte absorption and secretion.
description
1972 nî lūn-bûn
@nan
1972 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
1972 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
1972年の論文
@ja
1972年論文
@yue
1972年論文
@zh-hant
1972年論文
@zh-hk
1972年論文
@zh-mo
1972年論文
@zh-tw
1972年论文
@wuu
name
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@ast
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@en
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@nl
type
label
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@ast
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@en
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@nl
prefLabel
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@ast
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@en
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@nl
P2093
P2860
P356
P1476
Pathogenesis of congenital alk ...... lyte absorption and secretion.
@en
P2093
Bieberdorf FA
Fordtran JS
P2860
P304
P356
10.1172/JCI107002
P407
P577
1972-08-01T00:00:00Z