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MMAB gene

Known as: MMAB, ATP:cob(I)alamin adenosyltransferase, CFAP23 
 
National Institutes of Health

Papers overview

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2017
2017
Mutations in the human MMAA gene cause the metabolic disorder cblA-type methylmalonic aciduria (MMA), although knowledge of the… Expand
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2016
2016
Fungal infections claim an estimated 1.5 million lives each year. Mechanisms that protect from fungal infections are still… Expand
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2016
2016
Disseminated candidiasis has become one of the leading causes of hospital-acquired blood stream infections with high mobility and… Expand
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2016
2016
BackgroundSeveral genome-wide association studies have discovered novel loci at chromosome 12q24, which includes mevalonate… Expand
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2012
2012
The ubiquitin ligase Cbl-b is an established regulator of T cell immune response thresholds. We recently showed that adoptive… Expand
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2012
2012
Organ-specific birth defects are seen in patients with some inborn errors of vitamin B(12) metabolism. To determine whether three… Expand
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2012
2012
Ionic liquid crystals (ILCs), low-melting ionic compounds exhibiting mesophases, have attracted considerable interest because… Expand
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2010
2010
Genome-wide association studies (GWAS) have identified numerous loci associated with various complex traits for which the… Expand
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2009
2009
MMAB (methylmalonic aciduria type B) is a mitochondrial enzyme involved in the metabolism of vitamin B(12). It functions as the… Expand
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2004
2004
Methylmalonic acidemia (MMA) is caused by the deficient activity of l-methylmalonyl-CoA mutase, which is a vitamin B(12) (or… Expand
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