Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,496,984 papers from all fields of science
Search
Sign In
Create Free Account
SLC19A3 gene
Known as:
THTR2
, solute carrier family 19 member 3
, SLC19A3
Expand
National Institutes of Health
Create Alert
Alert
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Obesity status modifies the association between rs7556897T>C in the intergenic region SLC19A3-CCL20 and blood pressure in French children
S. El Shamieh
,
M. Stathopoulou
,
+10 authors
S. Visvikis-Siest
Clinical Chemistry and Laboratory Medicine
2020
Corpus ID: 214766623
Abstract Background Growing evidence reports an association between inflammatory markers, obesity and blood pressure (BP…
Expand
2016
2016
Novel SLC19A3 Promoter Deletion and Allelic Silencing in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy
I. Flønes
,
P. Sztromwasser
,
+9 authors
C. Tzoulis
PLoS ONE
2016
Corpus ID: 1854118
Background Biotin-thiamine responsive basal ganglia disease is a severe, but potentially treatable disorder caused by mutations…
Expand
2015
2015
Association of EP 2 receptor and SLC 19 A 3 in regulating breast cancer metastasis
I. Cheuk
,
V. Shin
,
+7 authors
A. Kwong
2015
Corpus ID: 120237788
Breast cancer is the most common cancer in women worldwide. Triple-negative breast cancer patients have higher metastatic rate…
Expand
2015
2015
Klinička raznolikost bolesti uzrokovane nasljednim mutacijama gena za prijenosnik tiamina-2 (ThTr2)
Lucija Debeljak
2015
Corpus ID: 89585581
Deficiency of thiamine transporter-2 is autosomal recessive hereditary disease caused by mutations in SLC19A3 gene on 2q26.3…
Expand
2014
2014
Whole exome sequencing reveals compound heterozygous mutations in SLC19A3 causing biotin-thiamine responsive basal ganglia disease
L. Sremba
,
R. Chang
,
N. Elbalalesy
,
E. J. Cambray-Forker
,
J. Abdenur
Molecular Genetics and Metabolism Reports
2014
Corpus ID: 17478313
2014
2014
Genetic variation of SLC19A3 is associated to diabetic retinopathy and nephropathy in type 1 diabetes
L. Toppila
,
M. Porta
,
+7 authors
Groop Ph
2014
Corpus ID: 81681049
2014
2014
Reply: Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable disease.
Mike Gerards
,
R. de Coo
,
H. Smeets
Brain : a journal of neurology
2014
Corpus ID: 8725662
Sir, The research articles ‘Exome sequencing reveals mutated SLC19A3 in patients with an early-infantile, lethal encephalopathy…
Expand
2012
2012
Disruption of Thiamine Uptake and Growth of Cells by Feline Leukemia Virus Subgroup A
R. Mendoza
,
A. Miller
,
J. Overbaugh
Journal of Virology
2012
Corpus ID: 35887173
ABSTRACT Feline leukemia virus (FeLV) is still a major cause of morbidity and mortality in domestic cats and some wild cats…
Expand
2011
2011
Title Quantitative analysis and diagnostic significance of methylated SLC 19 A 3 DNA in the plasma of breast and gastric cancer patients
E. Ng
,
C. Leung
,
+6 authors
A. Kwong
2011
Corpus ID: 73645499
Background: Previously, we have examined the methylation status of SLC19A3 (solute carrier family 19, member 3) promoter and…
Expand
2009
2009
1089 Promoter Hypermethylation Mediates Downregulation of Thiamin Receptor SLC19A3 But Not SLC19A2 in Gastric Cancer
Xin Liu
,
Hongchuan Jin
,
+6 authors
J. Sung
2009
Corpus ID: 72995693
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)
ACCEPT & CONTINUE