Cystathionine-synthase-deficient patients do not use the transamination pathway of methionine to reduce hypermethioninemia and homocystinemia
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism
Reference20 articles.
1. Disorders of transsulfuration;Mudd,1983
2. Biochemistry of sulfur-containing amino acids;Cooper;Annu Rev Biochem,1983
3. Evidence for alternative pathways of methionine catabolism;Benevenga;Adv Nutr Res,1984
4. Methionine degradation: “Anabolic and catabolic”;Livesey;Trends Biochem Sci,1984
5. Oxidative decarboxylation of 4-methyl thio-2-oxobutyrate by branched-chain 2-oxo acid dehydrogenase complex;Jones;Biochem J,1986
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2. Adenosine kinase deficiency: expanding the clinical spectrum and evaluating therapeutic options;Journal of Inherited Metabolic Disease;2015-12-07
3. Long-term betaine therapy in a murine model of cystathionine beta-synthase deficient homocystinuria: Decreased efficacy over time reveals a significant threshold effect between elevated homocysteine and thrombotic risk;Molecular Genetics and Metabolism;2012-03
4. The biochemical and toxicological significance of hypermethionemia: new insights and clinical relevance;Expert Opinion on Drug Metabolism & Toxicology;2010-09-28
5. Gender differences in methionine accumulation and metabolism in freshly isolated mouse hepatocytes: Potential roles in toxicity;Toxicology and Applied Pharmacology;2009-05-01
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