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SLC6A20 gene
Known as:
SLC6A20
, solute carrier family 6 member 20
, Xtrp3
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National Institutes of Health
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Related topics
Related topics
6 relations
SLC16A14 gene
SLC35F2 gene
SLC35F3 gene
SLC35F5 gene
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2015
2015
Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma
Jurjen J. Luykx
,
Steven C. Bakker
,
+19 authors
Roel A. Ophoff
Molecular Psychiatry
2015
The N-methyl-d-aspartate receptor (NMDAR) coagonists glycine, d-serine and l-proline play crucial roles in NMDAR-dependent…
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2014
2014
A Genome-Wide Association Study Identifies Potential Susceptibility Loci for Hirschsprung Disease
Jeong-Hyun Kim
,
Hyun Sub Cheong
,
+11 authors
Stacey Cherny
PloS one
2014
Hirschsprung disease (HSCR) is a congenital and heterogeneous disorder characterized by the absence of intramural nervous…
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2014
2014
A genetic variant in SLC6A20 is associated with Type 2 diabetes in white-European and Chinese populations.
Yan Ling
,
Thijs T. W. van Herpt
,
+10 authors
E J G Sijbrands
Diabetic medicine : a journal of the British…
2014
AIMS To investigate whether polymorphisms in SLC6A20 are associated with susceptibility to Type 2 diabetes. METHODS In the…
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2011
2011
Metabolomics reveals attenuation of the SLC6A20 kidney transporter in nonhuman primate and mouse models of type 2 diabetes mellitus.
Andrew D. Patterson
,
Jessica A. Bonzo
,
+8 authors
Frank J. Gonzalez
The Journal of biological chemistry
2011
To enhance understanding of the metabolic indicators of type 2 diabetes mellitus (T2DM) disease pathogenesis and progression, the…
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2010
2010
Genome-wide analysis of epigenetic signatures for kidney-specific transporters.
Ryota Kikuchi
,
Shintaro Yagi
,
Hiroyuki Kusuhara
,
Satoki Imai
,
Yuichi Sugiyama
,
Kunio Shiota
Kidney international
2010
DNA methylation-dependent gene silencing is one of the most characterized mechanisms in epigenetic regulation of gene expression…
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2009
2009
Sodium translocation by the iminoglycinuria associated imino transporter (SLC6A20).
Angelika Bröer
,
Sarojini Balkrishna
,
Gábor Kottra
,
S. A. Davis
,
Aaron J Oakley
,
Stefan Bröer
Molecular membrane biology
2009
The system IMINO transporter plays an essential role in the transport of proline and hydroxyproline in the intestine and kidney…
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2008
2008
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.
Stefan Bröer
,
Charles G. Bailey
,
+7 authors
John E J Rasko
The Journal of clinical investigation
2008
Iminoglycinuria (IG) is an autosomal recessive abnormality of renal transport of glycine and the imino acids proline and…
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2006
2006
Neutral amino acid transport mediated by ortholog of imino acid transporter SIT1/SLC6A20 in opossum kidney cells.
Zorica Ristic
,
Simone Camargo
,
+6 authors
François Verrey
American journal of physiology. Renal physiology
2006
Most neutral l-amino acid acids are transported actively across the luminal brush-border membrane of small intestine and kidney…
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2006
2006
Iminoglycinuria is not caused by mutations in SLC6A20 or SLC36A1
William A Gahl
,
Isa Bernardini
,
+5 authors
Robert Kleta
2006
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Highly Cited
2005
Highly Cited
2005
Identification of mammalian proline transporter SIT1 (SLC6A20) with characteristics of classical system imino.
Hitomi Takanaga
,
Bryan Mackenzie
,
Yoshiro Suzuki
,
M A Hediger
The Journal of biological chemistry
2005
Amino acid homeostasis depends on specific amino acid transport systems, many of which have been characterized at the molecular…
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