SLC25A19 gene

Known as: MITOCHONDRIAL THIAMINE PYROPHOSPHATE CARRIER, TPC, MUP1 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2002-2017
02420022017

Papers overview

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2016
2016
Many factors, such as must composition, juice clarification, fermentation temperature, or inoculated yeast strain, strongly… (More)
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Review
2016
Review
2016
INTRODUCTION Thiamine is a key cofactor for energy metabolism in brain tissue. There are four major genetic defects (SLC19A2… (More)
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2015
2015
microRNA-155 (miR-155) is one of the well-known oncogenic miRNA implicated in various types of tumors. Thiamine, commonly known… (More)
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2013
2013
An increased carbon flux and exploitation of metabolic pathways for the rapid generation of biosynthetic precursors is a common… (More)
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2013
2013
Transcriptional regulation of expression of the human mitochondrial thiamine pyrophosphate transporter (the product of the… (More)
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2010
2010
Amish microcephaly (MCPHA, OMIM #607196) is a metabolic disorder that has been previously characterized by severe infantile… (More)
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Review
2008
Review
2008
We review the evidence that the function of the SLC25A19 gene product, previously identified as the mitochondrial… (More)
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2006
2006
SLC25A19 mutations cause Amish lethal microcephaly (MCPHA), which markedly retards brain development and leads to alpha… (More)
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2003
2003
Sixteen unrelated Southern European patients with the mitochondrial depletion syndrome (MDS) were analyzed for mutations in the… (More)
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2002
2002
The disorder Amish microcephaly (MCPHA) is characterized by severe congenital microcephaly, elevated levels of α-ketoglutarate in… (More)
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