Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
about
Sugar binding residue affects apparent Na+ affinity and transport stoichiometry in mouse sodium/glucose cotransporter type 3BCloning and functional characterization of the human GLUT7 isoform SLC2A7 from the small intestine.Neutralization of a conserved amino acid residue in the human Na+/glucose transporter (hSGLT1) generates a glucose-gated H+ channel.A single amino acid change converts the sugar sensor SGLT3 into a sugar transporter.Inherited epithelial transporter disorders--an overview.Regulation of the human Na(+)-glucose cotransporter gene, SGLT1, by HNF-1 and Sp1.Use of systems pharmacology modeling to elucidate the operating characteristics of SGLT1 and SGLT2 in renal glucose reabsorption in humansMolecular characterization of Vibrio parahaemolyticus vSGLT: a model for sodium-coupled sugar cotransporters.Characterization of the Vibrio parahaemolyticus Na+/Glucose cotransporter. A bacterial member of the sodium/glucose transporter (SGLT) family.Multiple transcription factors in 5'-flanking region of human polymeric Ig receptor control its basal expression.Intestinal sugar transport.Functional role of specific amino acid residues in human thiamine transporter SLC19A2: mutational analysis.
P2860
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P2860
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
description
1999 nî lūn-bûn
@nan
1999 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@ast
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@en
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@nl
type
label
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@ast
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@en
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@nl
prefLabel
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@ast
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@en
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@nl
P2093
P1476
Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects
@en
P2093
B A Hirayama
B Steinmann
E M Wright
M G Martín
N U Bosshard
P304
P356
10.1016/S0925-4439(98)00109-4
P407
P577
1999-02-24T00:00:00Z