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MMAB gene

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

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Related topics

2 relations
Cob(I)alamin adenosyltransferaseMMAA gene

Papers overview

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2017
2017
Protein destabilization and loss of protein‐protein interaction are fundamental mechanisms in cblA‐type methylmalonic aciduria
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
Inhibition of CBLB protects from lethal Candida albicans sepsis
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
Targeting CBLB as a Potential Therapeutic Approach for Disseminated Candidiasis
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
Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population
BackgroundSeveral genome-wide association studies have discovered novel loci at chromosome 12q24, which includes mevalonate… Expand
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2012
2012
Adoptive Transfer of siRNA Cblb-Silenced CD8+ T Lymphocytes Augments Tumor Vaccine Efficacy in a B16 Melanoma Model
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
The methylmalonic aciduria related genes, Mmaa, Mmab, and Mut, are broadly expressed in placental and embryonic tissues during mouse organogenesis.
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
Photoinduced isothermal phase transition of ionic liquid crystals.
Ionic liquid crystals (ILCs), low-melting ionic compounds exhibiting mesophases, have attracted considerable interest because… Expand
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2010
2010
Allelic expression imbalance at high-density lipoprotein cholesterol locus MMAB-MVK.
Genome-wide association studies (GWAS) have identified numerous loci associated with various complex traits for which the… Expand
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2009
2009
Ligand-binding by catalytically inactive mutants of the cblB complementation group defective in human ATP:cob(I)alamin adenosyltransferase.
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
Mutation analysis of the MMAA and MMAB genes in Japanese patients with vitamin B(12)-responsive methylmalonic acidemia: identification of a prevalent MMAA mutation.
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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