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SLC6A20 gene

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

Papers overview

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2015
2015
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
Hirschsprung disease (HSCR) is a congenital and heterogeneous disorder characterized by the absence of intramural nervous… Expand
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2014
2014
AIMS To investigate whether polymorphisms in SLC6A20 are associated with susceptibility to Type 2 diabetes. METHODS In the… Expand
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2011
2011
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
DNA methylation-dependent gene silencing is one of the most characterized mechanisms in epigenetic regulation of gene expression… Expand
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2009
2009
The system IMINO transporter plays an essential role in the transport of proline and hydroxyproline in the intestine and kidney… Expand
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2008
2008
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
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
Amino acid homeostasis depends on specific amino acid transport systems, many of which have been characterized at the molecular… Expand
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