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SLC5A1 wt Allele

Known as: NAGT, SGLT1, Solute Carrier Family 5 (Sodium/Glucose Cotransporter), Member 1 wt Allele 
Human SLC5A1 wild-type allele is located in the vicinity of either 22q13.1 or 22q12.3 and is approximately 67 kb in length. This allele, which… Expand
National Institutes of Health

Papers overview

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Highly Cited
2014
Highly Cited
2014
Intestinal glucose absorption is mediated by SGLT1 whereas GLUT2 is considered to provide basolateral exit. Recently, it was… Expand
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Highly Cited
2011
Highly Cited
2011
To clarify the physiological role of Na+-d-glucose cotransporter SGLT1 in small intestine and kidney, Sglt1−/− mice were… Expand
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Highly Cited
2007
Highly Cited
2007
We tested whether the dominant intestinal sugar transporter GLUT2 was inhibited by intestinal luminal compounds that are… Expand
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Highly Cited
2000
Highly Cited
2000
Intestinal glucose uptake is mainly performed by the sodium-dependent glucose transporter, SGLT1. The transport activity of SGLT1… Expand
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Highly Cited
2000
Highly Cited
2000
Although it has been suggested that the intestinal glucose transporter may actively absorb dietary flavonoid glucosides, there is… Expand
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Highly Cited
1997
Highly Cited
1997
Tight junctions serve as the rate-limiting barrier to passive movement of hydrophilic solutes across intestinal epithelia. After… Expand
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Highly Cited
1996
Highly Cited
1996
Cotransporters harness ion gradients to drive ‘active’ transport of substrates into cells, for example, the Na+/glucose… Expand
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Highly Cited
1995
Highly Cited
1995
The distribution of beta 1,2 N-acetylglucosaminyltransferase I (NAGT I), alpha 1,3-1,6 mannosidase II (Mann II), beta 1,4… Expand
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Highly Cited
1994
Highly Cited
1994
We report the primary structure, functional characterization, and tissue distribution of the high affinity Na+/glucose… Expand
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Highly Cited
1991
Highly Cited
1991
GLUCOSE/galactose malabsorption (GGM) is an autosomal recessive disease manifesting within the first weeks of life and… Expand
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