Defects in Auxiliary Redox Proteins Lead to Functional Methionine Synthase Deficiency

This publication has 25 references indexed in Scilit:

• The Yin-Yang of cobalamin biochemistry
  Chemistry & Biology, 1997
• Human Methionine Synthase
  Journal of Biological Chemistry, 1997
• Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders
  Human Molecular Genetics, 1996
• Defects in human methionine synthase in cblG patients
  Human Molecular Genetics, 1996
• Hyperhomocyst(e)inemia as a Risk Factor for Occlusive Vascular Disease
  Annual Review of Nutrition, 1992
• Heterogeneity in cblG: Differential retention of cobalamin on methionine synthase
  Biochemical Medicine and Metabolic Biology, 1992
• Functional methionine synthase deficiency (cblE and cblG): Clinical and biochemical heterogeneity
  American Journal of Medical Genetics, 1989
• Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.
  Journal of Clinical Investigation, 1988
• Titanium (III) Citrate as a Nontoxic Oxidation-Reduction Buffering System for the Culture of Obligate Anaerobes
  Science, 1976
• N5-methyltetrahydrofolate: Homocysteine methyltransferase activity in extracts from normal, malignant and embryonic tissue culture cells
  Biochemical and Biophysical Research Communications, 1974