SLC25A22 gene

Known as: FLJ13044, SLC25A22, solute carrier family 25 member 22 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1987-2017
024619872017

Papers overview

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2017
2017
Mutations in SLC25A22 are known to cause neonatal epileptic encephalopathy and migrating partial seizures in infancy. Using whole… (More)
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2017
2017
The solute carrier family 25 (SLC25) drives the import of a large diversity of metabolites into mitochondria, a key cellular… (More)
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2017
2017
SLC25A22, which encodes the mitochondrial glutamate transporter, is overexpressed in colorectal cancer (CRC) and is essential for… (More)
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2016
2016
BACKGROUND & AIMS Many colorectal cancer (CRC) cells contain mutations in KRAS. Analyses of CRC cells with mutations in APC or… (More)
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2014
2014
In his writings on the milieu intérieur, Claude Bernard first hypothesized on the presence of feedback mechanisms within the cell… (More)
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2013
2013
OBJECTIVE To identify a genetic cause for migrating partial seizures in infancy (MPSI). METHODS We characterized a… (More)
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2013
2013
in the GenBank non-redundant DNA database was examined. Two additional cases of ISAba1 associated with distinct ampC alleles were… (More)
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2009
2009
Neonatal epileptic encephalopathies with suppression bursts (SBs) are very severe and relatively rare diseases characterized by… (More)
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Highly Cited
2005
Highly Cited
2005
Severe neonatal epilepsies with suppression-burst pattern are epileptic syndromes with either neonatal onset or onset during the… (More)
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1987
1987
The expression of the rat GH (rGH) gene is limited to the anterior pituitary. Using a DNase I footprinting assay, we have sought… (More)
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