MCCC1 gene

Known as: MCCA, 3-METHYLCROTONYL-CoA CARBOXYLASE 1, methylcrotonoyl-CoA carboxylase alpha 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1974-2017
02419742017

Papers overview

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2013
2013
Canonical correlation analysis (CCA) between recorded electroencephalogram (EEG) and designed reference signals of sine-cosine… (More)
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2013
2013
Multimodal brain imaging data have shown increasing utility in answering both scientifically interesting and clinically relevant… (More)
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2009
2009
We have characterized the master regulator of cysteine metabolism, CymR, in Staphylococcus aureus. CymR repressed the… (More)
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2008
2008
Synthetic phosphoramidate analogues of nucleosides have been used as enzyme inhibitors for decades and have therapeutic… (More)
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2007
2007
In bacterial c-type cytochromes, the haem cofactor is covalently attached via two cysteine residues organized in a haem c-binding… (More)
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2005
2005
Isolated 3-methylcrotonyl-CoA carboxylase (MCC) deficiency is an autosomal recessive disorder that appears to be the most… (More)
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2004
2004
Deficiency of 3-methylcrotonyl-CoA carboxylase (MCC) results in elevated excretion of 3-methylcrotonylglycine (3-MCG) and 3… (More)
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2001
2001
Isolated biotin-resistant 3-methylcrotonyl-CoA carboxylase (MCC) deficiency is an autosomal recessive disorder of leucine… (More)
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2001
2001
3-Methylcrotonyl-CoA: carboxylase (EC 6.4.1.4; MCC) deficiency is an inborn error of the leucine degradation pathway (MIM *210200… (More)
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1995
1995
The translation inhibitor microcin C7 (MccC7) is a linear heptapeptide whose N terminus has been replaced by an N-formyl group… (More)
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