These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
189 related articles for article (PubMed ID: 1059104)
1. Genetic complementation in heterokaryons of human fibroblasts defective in cobalamin metabolism. Gravel RA; Mahoney MJ; Ruddle FH; Rosenberg LE Proc Natl Acad Sci U S A; 1975 Aug; 72(8):3181-5. PubMed ID: 1059104 [TBL] [Abstract][Full Text] [Related]
2. Inborn errors of cobalamin metabolism: effect of cobalamin supplementation in culture on methylmalonyl CoA mutase activity in normal and mutant human fibroblasts. Willard HF; Rosenberg LE Biochem Genet; 1979 Feb; 17(1-2):57-75. PubMed ID: 36882 [TBL] [Abstract][Full Text] [Related]
3. Genetic complementation of propionyl-CoA carboxylase deficiency in cultured human fibroblasts. Gravel RA; Lam KF; Scully KJ; Hsia Y Am J Hum Genet; 1977 Jul; 29(4):378-88. PubMed ID: 195466 [TBL] [Abstract][Full Text] [Related]
4. Differential diagnosis of mut and cbl methylmalonic aciduria by DNA-mediated gene transfer in primary fibroblasts. Wilkemeyer MF; Crane AM; Ledley FD J Clin Invest; 1991 Mar; 87(3):915-8. PubMed ID: 1671869 [TBL] [Abstract][Full Text] [Related]
5. Rapid prenatal and postnatal detection of inborn errors of propionate, methylmalonate, and cobalamin metabolism: a sensitive assay using cultured cells. Willard HF; Ambani LM; Hart AC; Mahoney MJ; Rosenberg LE Hum Genet; 1976 Dec; 34(3):277-83. PubMed ID: 1002151 [TBL] [Abstract][Full Text] [Related]
6. Inherited methylmalonyl CoA mutase apoenzyme deficiency in human fibroblasts: evidence for allelic heterogeneity, genetic compounds, and codominant expression. Willard HF; Rosenberg LE J Clin Invest; 1980 Mar; 65(3):690-8. PubMed ID: 6101601 [TBL] [Abstract][Full Text] [Related]
7. Methylmalonicacidemia: biochemical heterogeneity in defects of 5'-deoxyadenosylcobalamin synthesis. Mahoney MJ; Hart AC; Steen VD; Rosenberg LE Proc Natl Acad Sci U S A; 1975 Jul; 72(7):2799-803. PubMed ID: 1058495 [TBL] [Abstract][Full Text] [Related]
8. Identification of ABC transporters acting in vitamin B McDonald MK; Fritz JA; Jia D; Scheuchner D; Snyder FF; Stanislaus A; Curle J; Li L; Stabler SP; Allen RH; Mains PE; Gravel RA Mol Genet Metab; 2017 Dec; 122(4):160-171. PubMed ID: 29153845 [TBL] [Abstract][Full Text] [Related]
10. Causes of and diagnostic approach to methylmalonic acidurias. Fowler B; Leonard JV; Baumgartner MR J Inherit Metab Dis; 2008 Jun; 31(3):350-60. PubMed ID: 18563633 [TBL] [Abstract][Full Text] [Related]
11. Clustering of mutations in methylmalonyl CoA mutase associated with mut- methylmalonic acidemia. Crane AM; Ledley FD Am J Hum Genet; 1994 Jul; 55(1):42-50. PubMed ID: 7912889 [TBL] [Abstract][Full Text] [Related]
12. The natural history of the inherited methylmalonic acidemias. Matsui SM; Mahoney MJ; Rosenberg LE N Engl J Med; 1983 Apr; 308(15):857-61. PubMed ID: 6132336 [TBL] [Abstract][Full Text] [Related]
13. Metabolic cooperation among cell lines from patients with inborn errors of vitamin B12 metabolism: differential response of cblC and cblD. Byck S; Rosenblatt DS Clin Invest Med; 1991 Apr; 14(2):153-9. PubMed ID: 1676355 [TBL] [Abstract][Full Text] [Related]
14. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism. Schuh S; Rosenblatt DS; Cooper BA; Schroeder ML; Bishop AJ; Seargeant LE; Haworth JC N Engl J Med; 1984 Mar; 310(11):686-90. PubMed ID: 6700644 [TBL] [Abstract][Full Text] [Related]
15. Transcobalamin in cultured fibroblasts from patients with inborn errors of vitamin B12 metabolism. Yamani L; Gibbs BF; Gilfix BM; Watkins D; Hosack A; Rosenblatt DS Mol Genet Metab; 2008; 95(1-2):104-6. PubMed ID: 18606554 [TBL] [Abstract][Full Text] [Related]
16. Cobalamin binding and cobalamin-dependent enzyme activity in normal and mutant human fibroblasts. Mellman I; Willard HF; Rosenberg LE J Clin Invest; 1978 Nov; 62(5):952-60. PubMed ID: 30783 [TBL] [Abstract][Full Text] [Related]
18. Recent advances in the inherited methylmalonic acidemias. Mahoney MJ; Bick D Acta Paediatr Scand; 1987 Sep; 76(5):689-96. PubMed ID: 2889315 [TBL] [Abstract][Full Text] [Related]
19. Inborn Error of Cobalamin Metabolism Associated with the Intracellular Accumulation of Transcobalamin-Bound Cobalamin and Mutations in ZNF143, Which Codes for a Transcriptional Activator. Pupavac M; Watkins D; Petrella F; Fahiminiya S; Janer A; Cheung W; Gingras AC; Pastinen T; Muenzer J; Majewski J; Shoubridge EA; Rosenblatt DS Hum Mutat; 2016 Sep; 37(9):976-82. PubMed ID: 27349184 [TBL] [Abstract][Full Text] [Related]
20. Recognition of two intracellular cobalamin binding proteins and their identification as methylmalonyl-CoA mutase and methionine synthetase. Kolhouse JF; Allen RH Proc Natl Acad Sci U S A; 1977 Mar; 74(3):921-5. PubMed ID: 15259 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]