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SLC19A3 gene

Known as: THTR2, solute carrier family 19 member 3, SLC19A3 
National Institutes of Health

Papers overview

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2020
2020
Abstract Background Growing evidence reports an association between inflammatory markers, obesity and blood pressure (BP… 
2016
2016
Background Biotin-thiamine responsive basal ganglia disease is a severe, but potentially treatable disorder caused by mutations… 
2015
2015
Breast cancer is the most common cancer in women worldwide. Triple-negative breast cancer patients have higher metastatic rate… 
2015
2015
Deficiency of thiamine transporter-2 is autosomal recessive hereditary disease caused by mutations in SLC19A3 gene on 2q26.3… 
2014
2014
Sir, The research articles ‘Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathy… 
2012
2012
ABSTRACT Feline leukemia virus (FeLV) is still a major cause of morbidity and mortality in domestic cats and some wild cats… 
2011
2011
Background: Previously, we have examined the methylation status of SLC19A3 (solute carrier family 19, member 3) promoter and…