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SLC3A1 gene

Known as: SOLUTE CARRIER FAMILY 3 (CYSTINE, DIBASIC, AND NEUTRAL AMINO ACID TRANSPORTER), MEMBER 1, solute carrier family 3 member 1, RBAT 
This gene is involved in the transport of amino acids.
National Institutes of Health

Papers overview

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2018
2018
BACKGROUND Cystinuria is a rare inherited renal stone disease caused by mutations in the SLC3A1 and SLC7A9 genes. The Chinese… 
2016
2016
Introduction. Available information about the impact of the polymorphic structure of type 1 angiotensin receptor (ATR1) gene on… 
2015
2015
AbstractCystinuria is an autosomal inherited disorder of renal reabsorption of cystine, arginine, lysine, and ornithine… 
2015
2015
Cystinuria, one of the first inborn errors of metabolism, is characterized by hyperexcretion of cystine, arginine, lysine, and… 
2010
2010
AIM To analyze the impact of polymorphism of a group of genes encoding for endothelial function on the development of target… 
2010
2010
Groundwater is of utmost significance to socioeconomic development and ecological recovery for the Loess Plateau. However… 
2009
2009
Background. We have previously demonstrated a glomerulo-tubular ‘crosstalk’ operating in the pathogenesis of tubulointerstitial… 
2005
2005
La cistinuria es una aminoaciduria hereditaria autosomica recessiva (tipus I, OMIM 220100) i dominant amb penetranca incompleta… 
1996
1996
We have established rBAT (named as SLC3A1 in the Genome Data Base) as a gene responsible for cystinuria, a heritable disorder of… 
Review
1987
Review
1987
Formulation of diets to a specified metabolisable energy (ME) is of major importance for the productivity of broiler chickens…