MLYCD gene

Known as: MALONYL-CoA DECARBOXYLASE, MLYCD, MCD 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2006-2016
02420062016

Papers overview

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2017
2017
We evaluate the clinical findings and the treatment response of a late-diagnosed case with a novel homozygous insertion c… (More)
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2016
2016
Differentially expressed genes in the left atria of mitral regurgitation (MR) pigs have been linked to peroxisome proliferator… (More)
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2015
2015
Nordihydroguaiaretic acid (NDGA), the main metabolite of Creosote bush, has been shown to have profound effects on the core… (More)
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2015
2015
BACKGROUND Malonyl-CoA decarboxylase (MLYCD, EC 4.1.1.9) deficiency is a rare autosomal recessive disorder that is widely… (More)
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2014
2014
Utilizing molecular data to derive functional physiological models tailored for specific cancer cells can facilitate the use of… (More)
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2012
2012
Effect of cinnamaldehyde (CD), 4-hydroxy-3-methoxy cinnamaldehyde (HMCD) and 3,5-dimethoxy-4-hydroxy cinnamaldehyde (HDMCD) on… (More)
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2012
2012
A 3-year-old Chinese boy presented with prominent clinical features of malonic aciduria, including developmental delay, short… (More)
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2012
2012
BACKGROUND Fatty acids provide energy and structural substrates for the heart and brain and may influence resuscitation from… (More)
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2010
2010
Malonyl coenzyme A (CoA) decarboxylase (EC 4.1.1.9, MCD) deficiency, or malonic aciduria, is a rare inborn error of metabolism… (More)
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2006
2006
Malonyl-CoA decarboxylase (MCD) deficiency is an extremely rare inborn error of metabolism that presents with metabolic acidosis… (More)
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