SLC52A2 gene

Known as: SOLUTE CARRIER FAMILY 52 (RIBOFLAVIN TRANSPORTER), MEMBER 2, RFVT2, PERV-A RECEPTOR 1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2005-2018
02420052018

Papers overview

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2016
2016
While it is well recognized that riboflavin accumulates in breast milk as an essential vitamin for neonates, transport mechanisms… (More)
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2016
2016
Ataxia is a symptom that is often associated with syndromic inherited diseases. We previously reported the linkage of a novel… (More)
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Review
2016
Review
2016
AIM Mutations in the genes encoding the riboflavin transporters RFVT2 and RFVT3 have been identified in Brown-Vialetto-Van Laere… (More)
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2015
2015
PURPOSE To generate a comprehensive "Secretome" of proteins potentially found in the blood and derive a virtual Affymetrix array… (More)
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2015
2015
Purpose: To generate a comprehensive "Secretome" of proteins potentially found in the blood and derive a virtual Affymetrix array… (More)
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2014
2014
Childhood onset motor neuron diseases or neuronopathies are a clinically heterogeneous group of disorders. A particularly severe… (More)
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2014
2014
OBJECTIVE As clinical studies conducted to explore the safety and efficacy of new procedures are considered an important focus in… (More)
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Review
2013
Review
2013
Riboflavin, a water-soluble vitamin also known as vitamin B2, is essential for normal cellular functions. Riboflavin transporters… (More)
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2012
2012
Clinical reports stating the efficacy of novel root canal disinfection protocols are an important focus in endodontic research… (More)
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2010
2010
We isolated cDNA coding a new human riboflavin transporter (hRFT)3, which exhibits 86.7 and 44.1% amino acid identity with hRFT1… (More)
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