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Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Nature genetics, 2006-01, Vol.38 (1), p.93-100

2006

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Seven novel mutations in mut methylmalonic aciduria

Human mutation, 1998, Vol.11 (4), p.270-274

1998

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Hyperhomocysteinemia Due to Methionine Synthase Deficiency, cblG: Structure of the MTR Gene, Genotype Diversity, and Recognition of a Common Mutation, P1173L

American journal of human genetics, 2002-07, Vol.71 (1), p.143-153

2002

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Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B 12 metabolism

Molecular genetics and metabolism, 2008-09, Vol.95 (1), p.104-106

2008

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Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B sub(12 metabolism)

Molecular genetics and metabolism, 2008-10, Vol.95 (1-2), p.104-106

2008

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Parallel changes in metabolite and expression profiles in crooked-tail mutant and folate-reduced wild-type mice

Human molecular genetics, 2006-12, Vol.15 (23), p.3387-3393

2006

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Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B12 metabolism

Molecular genetics and metabolism, 2008-09, Vol.95 (1-2), p.104-106

2008

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Homocysteine levels in A/J and C57BL/6J mice: genetic, diet, gender, and parental effects

Physiological genomics, 2005-05, Vol.21 (3), p.404-410

2005

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Nutrigenes, Functional Genomics and Systems Biology1

The Journal of nutrition, 2003-12, Vol.133 (12), p.4267

2003

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Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Nature genetics, 2006-08, Vol.38 (8), p.957-957

2006

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Nutrigenes, Functional Genomics and Systems Biology

The Journal of nutrition, 2003-12, Vol.133 (12), p.4267-4268

2003

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Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cb1C type

Nature genetics, 2006, Vol.38 (1), p.93-100

2006

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A common mutation among blacks with mut− methylmalonic aciduria

Human mutation, 1998, Vol.11 (S1), p.S248-S250

1998

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Genetic and molecular control of folate-homocysteine metabolism in mutant mice

Mammalian genome, 2002-05, Vol.13 (5), p.259-267

2002

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Seven novel mutations inmut methylmalonic aciduria

Human mutation, 1998, Vol.11 (4), p.270-274

1998

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Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism

Science (American Association for the Advancement of Science), 1985-06, Vol.228 (4705), p.1319-1321

1985

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Expression of transcobalamin II by amniocytes

Prenatal diagnosis, 1987-01, Vol.7 (1), p.35-39

1987

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Defect in Vitamin B 12 Release from Lysosomes: Newly Described Inborn Error of Vitamin B 12 Metabolism

Science (American Association for the Advancement of Science), 1985-06, Vol.228 (4705), p.1319-1321

1985

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Defect in Vitamin B$_{12}$ Release from Lysosomes: Newly Described Inborn Error of Vitamin B$_{12}$ Metabolism

Science (American Association for the Advancement of Science), 1985-06, Vol.228 (4705), p.1319-1321

1985

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Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Seven novel mutations in mut methylmalonic aciduria

Hyperhomocysteinemia Due to Methionine Synthase Deficiency, cblG: Structure of the MTR Gene, Genotype Diversity, and Recognition of a Common Mutation, P1173L

Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B 12 metabolism

Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B sub(12 metabolism)

Parallel changes in metabolite and expression profiles in crooked-tail mutant and folate-reduced wild-type mice

Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B12 metabolism

Homocysteine levels in A/J and C57BL/6J mice: genetic, diet, gender, and parental effects

Nutrigenes, Functional Genomics and Systems Biology1

Erratum: Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type

Nutrigenes, Functional Genomics and Systems Biology

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cb1C type

A common mutation among blacks with mut− methylmalonic aciduria

Genetic and molecular control of folate-homocysteine metabolism in mutant mice

Seven novel mutations inmut methylmalonic aciduria

Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism

Expression of transcobalamin II by amniocytes

Defect in Vitamin B 12 Release from Lysosomes: Newly Described Inborn Error of Vitamin B 12 Metabolism

Defect in Vitamin B$_{12}$ Release from Lysosomes: Newly Described Inborn Error of Vitamin B$_{12}$ Metabolism

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