methylcyanocarbamate dimer

Known as: MCCD 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1989-2016
01219892016

Papers overview

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2016
2016
We present the main results of the performance test campaign of the Mid-Infrared European Extremely Large Telescope Imager and… (More)
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2015
2015
Purpose:3-Methylcrotonyl-CoA carboxylase deficiency (MCCD) is an autosomal recessive disorder of leucine catabolism that has a… (More)
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2014
2014
Translation inhibitor microcin C (McC) is a heptapeptide with an aspartate α-carboxyl group linked to AMP via phosphoramidate… (More)
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2014
2014
OBJECTIVE 3-Methylcrotonyl-coenzyme A carboxylase deficiency (MCCD) is an autosomal recessive inborn error of leucine catabolism… (More)
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2009
2009
Polycystic kidney diseases result from disruption of the genetically defined program that controls the size and geometry of renal… (More)
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2006
2006
New technology enables expansion of newborn screening (NBS) of inborn errors aimed to prevent adverse outcome. In conditions with… (More)
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2000
2000
To determine the incidence of campylobacters in Northern Ireland pigs, ileal contents and anal swabs were taken shortly after… (More)
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1993
1993
 
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1992
1992
Counts of thermophilic campylobacters from 31 different waste water samples were parallel estimated with two different… (More)
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1989
1989
 
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