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SLC6A19 gene

Known as: Hartnup disease, SLC6A19, solute carrier family 6 member 19 
National Institutes of Health

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Hartnup DiseaseSLC6A20 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Amino acid restriction through B0ATI (Slc6a19) Inhibition: A potential target for treating diabetes
2018
2018
SLC6A19 is a novel putative gene, induced by dioxins via AhR in human hepatoma HepG2 cells.
2016
2016
Expression of apical Na+–l-glutamine co-transport activity, B0-system neutral amino acid co-transporter (B0AT1) and angiotensin-converting enzyme 2 along the jejunal crypt–villus axis in young pigs…
Gut apical amino acid (AA) transport activity is high at birth and during suckling, thus being essential to maintain luminal… 
2011
2011
Stimulation of the amino acid transporter SLC6A19 by JAK2.
2010
2010
SLC6A19 Minisatellites 7(SLC6A19-MS7)의 심근경색과의 관련성과 진화적 분석
2008
2008
Brandsch, M. 2006. Transport of L-proline, L-proline-containing peptides and related drugs at mammalian epithelial cell membranes. Amino Acids 31:119-136. Brandsch, M. und Brandsch, C. 2003…
Weiterführende Literatur findet sich in den anliegenden Publikationen. transport across the human intestinal epithelial (Caco-2… 
Highly Cited
2006
Highly Cited
2006
The Serum and Glucocorticoid Inducible Kinases SGK1-3 Stimulate the Neutral Amino Acid Transporter SLC6A19
The neutral amino acid transporter SLC6A19 (B⁰AT1) plays a decisive role in transport of neutral amino acids in the kidney and… 
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