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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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2014
2014
Hirschsprung disease (HSCR) is a congenital and heterogeneous disorder characterized by the absence of intramural nervous… 
2014
2014
To investigate whether polymorphisms in SLC6A20 are associated with susceptibility to Type 2 diabetes. 
Review
2012
Review
2012
The choroid plexus (CP) is a highly vascularized tissue in the brain ventricles and acts as the blood-cerebrospinal fluid (CSF… 
Highly Cited
2011
Highly Cited
2011
To enhance understanding of the metabolic indicators of type 2 diabetes mellitus (T2DM) disease pathogenesis and progression, the… 
2010
2010
DNA methylation-dependent gene silencing is one of the most characterized mechanisms in epigenetic regulation of gene expression… 
2009
2009
The system IMINO transporter plays an essential role in the transport of proline and hydroxyproline in the intestine and kidney… 
Highly Cited
2008
Highly Cited
2008
Iminoglycinuria (IG) is an autosomal recessive abnormality of renal transport of glycine and the imino acids proline and… 
2006
2006
Most neutral l-amino acid acids are transported actively across the luminal brush-border membrane of small intestine and kidney… 
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…