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MMAB gene

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

Related topics

Related topics

2 relations
Cob(I)alamin adenosyltransferaseMMAA gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
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
Highly Cited
2016
Highly Cited
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
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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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
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
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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