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methylcyanocarbamate dimer

Known as: MCCD 
 
National Institutes of Health

Papers overview

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2019
2019
Reduction of sulfite to sulfide is an essential step in the biogeochemical sulfur cycle. The Epsilonproteobacterium Wolinella… Expand
2016
2016
To mimic multilevel nerve root compression and intervertebral foramina stenosis in human, we established a new animal model of… Expand
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2015
2015
Purpose:3-Methylcrotonyl-CoA carboxylase deficiency (MCCD) is an autosomal recessive disorder of leucine catabolism that has a… Expand
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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… Expand
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2014
2014
OBJECTIVE 3-Methylcrotonyl-coenzyme A carboxylase deficiency (MCCD) is an autosomal recessive inborn error of leucine catabolism… Expand
2012
2012
OBJECTIVES The aims of this study were to evaluate whether there are changes in lung volumes, capnography, pulse oximetry and… Expand
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2011
2011
The study was conducted to find out errors in the medical certification of cause of death during July 2011 at a new teaching… Expand
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2010
2010
Statistics of mortality is an apart of vital registration system. Registraction system ie. fertility, mortality, merriage and… Expand
2007
2007
Significant changes in the sawtooth period have been observed on the Alcator C-Mod tokamak during phased ion cyclotron range of… Expand
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Highly Cited
2006
Highly Cited
2006
New technology enables expansion of newborn screening (NBS) of inborn errors aimed to prevent adverse outcome. In conditions with… Expand