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9 in total

1. Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver.

Authors: I S Mellman; P Youngdahl-Turner; H F Willard; L E Rosenberg
Journal: Proc Natl Acad Sci U S A Date: 1977-03 Impact factor: 11.205

2. Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesis.

Authors: M J Mahoney; A C Hart; V D Steen; L E Rosenberg
Journal: Proc Natl Acad Sci U S A Date: 1975-07 Impact factor: 11.205

3. Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.

Authors: H F Willard; I S Mellman; L E Rosenberg
Journal: Am J Hum Genet Date: 1978-01 Impact factor: 11.025

4. Genetic control of cobalamin binding in normal and mutant cells: assignment of the gene for 5-methyltetrahydrofolate:L-homocysteine S-methyltransferase to human chromosome 1.

Authors: I S Mellman; P F Lin; F H Ruddle; L E Rosenberg
Journal: Proc Natl Acad Sci U S A Date: 1979-01 Impact factor: 11.205

5. Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.

Authors: C Melissa Dobson; Timothy Wai; Daniel Leclerc; Aaron Wilson; Xuchu Wu; Carole Doré; Thomas Hudson; David S Rosenblatt; Roy A Gravel
Journal: Proc Natl Acad Sci U S A Date: 2002-11-15 Impact factor: 11.205

Synthesis of cobalamin coenzymes by human cells in tissue culture.

1. Intracellular binding of radioactive hydroxocobalamin to cobalamin-dependent apoenzymes in rat liver.

2. Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesis.

3. Genetic complementation among inherited deficiencies of methylmalonyl-CoA mutase activity: evidence for a new class of human cobalamin mutant.

4. Genetic control of cobalamin binding in normal and mutant cells: assignment of the gene for 5-methyltetrahydrofolate:L-homocysteine S-methyltransferase to human chromosome 1.

5. Identification of the gene responsible for the cblA complementation group of vitamin B12-responsive methylmalonic acidemia based on analysis of prokaryotic gene arrangements.

6. Methylmalonic acidemia controlled with oral administration of vitamin B12.

7. Treatment of the cbl B form of methylmalonic acidaemia with adenosylcobalamin.

8. Characterization of functional domains of the cblD (MMADHC) gene product.

9. Accurate assessment and identification of naturally occurring cellular cobalamins.