SLC22A5 gene

Known as: solute carrier family 22 member 5, SCD, SLC22A5 
 
National Institutes of Health

Papers overview

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Review
2013
Review
2013
The carnitine/organic cation transporter (OCTN) family consists of three transporter isoforms, i.e. OCTN1 (SLC22A4) and OCTN2… (More)
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Highly Cited
2009
Highly Cited
2009
Cisplatin is one of the most widely used anticancer agents for the treatment of solid tumors. The clinical use of cisplatin is… (More)
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Highly Cited
2007
Highly Cited
2007
Eukaryotic gene transcription is accompanied by acetylation and methylation of nucleosomes near promoters, but the locations and… (More)
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Highly Cited
2006
Highly Cited
2006
A vast number of drugs are subjected to active or facilitated transport and multiple transport mechanism may contribute to the… (More)
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2005
2005
Urinary excretion of cationic xenobiotics is believed to be mediated by organic cation transporter (OCT and OCTN) families… (More)
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2001
2001
1. The release of acetylcholine was investigated in the human placenta villus, a useful model for the characterization of the non… (More)
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2001
2001
OCTN2 is an Na-dependent transporter for carnitine, which is essential for fatty acid metabolism, and its functional defect leads… (More)
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2000
2000
This report describes the structure, function, and tissue distribution pattern of rat OCTN1 (novel organic cation transporter 1… (More)
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Highly Cited
1999
Highly Cited
1999
Primary systemic carnitine deficiency (SCD; OMIM 212140) is an autosomal recessive disorder characterized by progressive… (More)
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Highly Cited
1998
Highly Cited
1998
Primary carnitine deficiency, because of a defect of the tissue plasma membrane carnitine transporters, causes critical symptoms… (More)
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