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SLC6A20 gene

Known as: SLC6A20, solute carrier family 6 member 20, Xtrp3 
 
National Institutes of Health

Related topics

Related topics

6 relations
SLC16A14 geneSLC35F2 geneSLC35F3 geneSLC35F5 gene
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Proline Absorption and SGK1 Expression are Inhibited in Intestinal Tis7 Transgenic Mice
Background/Aims: Expression of the transcriptional co-regulator tis7 is markedly increased in the adaptive small intestine in a… Expand
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2015
2015
Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma
The N-methyl-d-aspartate receptor (NMDAR) coagonists glycine, d-serine and l-proline play crucial roles in NMDAR-dependent… Expand
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2014
2014
A Genome-Wide Association Study Identifies Potential Susceptibility Loci for Hirschsprung Disease
Hirschsprung disease (HSCR) is a congenital and heterogeneous disorder characterized by the absence of intramural nervous… Expand
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2014
2014
A genetic variant in SLC6A20 is associated with Type 2 diabetes in white‐European and Chinese populations
To investigate whether polymorphisms in SLC6A20 are associated with susceptibility to Type 2 diabetes. 
Highly Cited
2011
Highly Cited
2011
Metabolomics Reveals Attenuation of the SLC6A20 Kidney Transporter in Nonhuman Primate and Mouse Models of Type 2 Diabetes Mellitus*
To enhance understanding of the metabolic indicators of type 2 diabetes mellitus (T2DM) disease pathogenesis and progression, the… Expand
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2010
2010
Genome-wide analysis of epigenetic signatures for kidney-specific transporters.
DNA methylation-dependent gene silencing is one of the most characterized mechanisms in epigenetic regulation of gene expression… Expand
2009
2009
Sodium translocation by the iminoglycinuria associated imino transporter (SLC6A20)
The system IMINO transporter plays an essential role in the transport of proline and hydroxyproline in the intestine and kidney… Expand
Highly Cited
2008
Highly Cited
2008
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.
Iminoglycinuria (IG) is an autosomal recessive abnormality of renal transport of glycine and the imino acids proline and… Expand
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2006
2006
Neutral amino acid transport mediated by ortholog of imino acid transporter SIT1/SLC6A20 in opossum kidney cells.
Most neutral l-amino acid acids are transported actively across the luminal brush-border membrane of small intestine and kidney… Expand
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Highly Cited
2005
Highly Cited
2005
Identification of Mammalian Proline Transporter SIT1 (SLC6A20) with Characteristics of Classical System Imino*
Amino acid homeostasis depends on specific amino acid transport systems, many of which have been characterized at the molecular… Expand
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