Skip to search formSkip to main contentSkip to account menu

SLC22A5 gene

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

Related topics

Related topics

2 relations
Renal carnitine transport defectSLC22A2 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
Up-regulation of hepatic fatty acid transporters and inhibition/down-regulation of hepatic OCTN2 contribute to olanzapine-induced liver steatosis.
2010
2010
Quantitative structure activity relationship for inhibition of human organic cation/carnitine transporter.
Organic cation/carnitine transporter (OCTN2; SLC22A5) is an important transporter for L-carnitine homeostasis, but can be… 
2010
2010
OCTN2 is associated with carnitine transport capacity of rat skeletal muscles
Aim:  Carnitine plays an essential role in fat oxidation in skeletal muscles; therefore carnitine influx could be crucial for… 
2008
2008
The inhibitory effects of fluoroquinolones on L-carnitine transport in placental cell line BeWo.
2007
2007
OCTN2-mediated carnitine uptake in a newly discovered human proximal tubule cell line (Caki-1).
The proximal tubular reabsorption of carnitine in the human kidney is significant because more than 95% of the carnitine filtered… 
2005
2005
SATURABLE DISTRIBUTION OF TACRINE INTO THE STRIATAL EXTRACELLULAR FLUID OF THE RAT: EVIDENCE OF INVOLVEMENT OF MULTIPLE ORGANIC CATION TRANSPORTERS IN THE TRANSPORT
The kinetics and mechanism by which tacrine is distributed in the rat brain were examined. Tacrine levels in plasma and striatal… 
2005
2005
Carnitine/organic cation transporter OCTN2-mediated transport of carnitine in primary-cultured epididymal epithelial cells.
Carnitine is essential for the acquisition of motility and maturation of spermatozoa in the epididymis, and is accumulated in… 
2003
2003
Downregulation of carnitine acyltransferases and organic cation transporter OCTN2 in mononuclear cells in healthy elderly and patients with myelodysplastic syndromes
Changes in key enzymes of oxidative metabolism at the mitochondrial level are known to be associated with the aging process… 
2003
2003
Functional Domains in the Carnitine Transporter OCTN2, Defective in Primary Carnitine Deficiency*
Primary carnitine deficiency is an autosomal recessive disorder of fatty acid oxidation characterized by hypoketotic hypoglycemia… 
2002
2002
Age-associated cardiomyopathy in heterozygous carrier mice of a pathological mutation of carnitine transporter gene, OCTN2.
The purpose of this study was to test whether heterozygotes of juvenile visceral steatosis mice, a model for systemic carnitine… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)