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SLC6A18 gene

Known as: Xtrp2, solute carrier family 6 member 18, FLJ31236 
 
National Institutes of Health

Papers overview

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2019
2019
Several genes lost in the ancestors of whales and dolphins likely contributed to adapting to a fully aquatic environment. The… Expand
2019
2019
Myopia is one of the most common ocular disorders in the world, yet the genetic etiology of the disease remains poorly understood… Expand
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2019
2019
Myopia is one of the most common ocular disorders in the world, yet the genetic etiology of the disease remains poorly understood… Expand
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2018
2018
The mRNA expressions of the epithelial neutral amino acid transporters slc6a18 and slc6a19a in the five segments (HL, PMC, GL… Expand
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2011
2011
OBJECTIVE SLC6A18 (solute carrier family 6, member 18) acts as a specific transporter for neurotransmitters, amino acids and… Expand
2010
2010
Renal maturation occurs post-natally in many species and reabsorption capacity at birth can vary substantially from the mature… Expand
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2009
2009
The orphan transporter Slc6a18 (XT2) is highly expressed at the luminal membrane of kidney proximal tubules and displays ∼50… Expand
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2009
2009
* These authors contributed equally to this work 1 Institute of Physiology and Center for Integrative Human Physiology (ZIHP… Expand
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2006
2006
We investigated the possible association of solute carrier family 6 member 18 (SLC6A18) with hypertension and blood pressure in… 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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