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HLCS gene

Known as: HCS, HLCS, HOLOCARBOXYLASE SYNTHETASE 
 
National Institutes of Health

Papers overview

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2011
2011
Previous studies suggest that histones H3 and H4 are posttranslationally modified by binding of the vitamin biotin, catalyzed by… Expand
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2009
2009
Biotin influences transcription in organisms from bacteria to humans. The enzyme, biotin protein ligase, which catalyzes post… Expand
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Highly Cited
2008
Highly Cited
2008
The sodium-dependent multivitamin transporter (SMVT) is essential for mediating and regulating biotin entry into mammalian cells… Expand
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Highly Cited
2008
Highly Cited
2008
Biotinylation is a recent addition to the list of reported posttranslational modifications made to histones. Holocarboxylase… Expand
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2007
2007
Protein biotinylation is an original and very specific posttranslational modification, compartmented in plants, between… Expand
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2007
2007
SummaryCarnitine transporter deficiency (CTD) and holocarboxylase synthetase deficiency (HLCSD) are frequent in The Faroe Islands… Expand
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Review
2005
Review
2005
Holocarboxylase synthetase (HLCS) deficiency is an autosomal recessive disorder. HLCS is an enzyme that catalyzes biotin… Expand
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2005
2005
In evaluating potential indicators of biotin status, we quantitated the expression of biotin-related genes in leukocytes from… Expand
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2001
2001
Biotin is the cofactor of carboxylases [pyruvate (PC), propionyl-CoA (PCC), 3-methyl crotonyl-CoA and acetyl-CoA], to which it is… Expand
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1981
1981
Biotin-responsive multiple carboxylase deficiency is an inherited disorder of organic acid metabolism in man in which there are… Expand
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