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.
3. Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6. Ledley FD; Lumetta MR; Zoghbi HY; VanTuinen P; Ledbetter SA; Ledbetter DH Am J Hum Genet; 1988 Jun; 42(6):839-46. PubMed ID: 2897160 [TBL] [Abstract][Full Text] [Related]
4. Correction of methylmalonyl-CoA mutase deficiency in Mut0 fibroblasts and constitution of gene expression in primary human hepatocytes by retroviral-mediated gene transfer. Sawada T; Ledley FD Somat Cell Mol Genet; 1992 Nov; 18(6):507-16. PubMed ID: 1363156 [TBL] [Abstract][Full Text] [Related]
5. Heterogeneous alleles and expression of methylmalonyl CoA mutase in mut methylmalonic acidemia. Ledley FD; Crane AM; Lumetta M Am J Hum Genet; 1990 Mar; 46(3):539-47. PubMed ID: 1968706 [TBL] [Abstract][Full Text] [Related]
6. Expression of recombinant human methylmalonyl-CoA mutase: in primary mut fibroblasts and Saccharomyces cerevisiae. Andrews E; Jansen R; Crane AM; Cholin S; McDonnell D; Ledley FD Biochem Med Metab Biol; 1993 Oct; 50(2):135-44. PubMed ID: 7903149 [TBL] [Abstract][Full Text] [Related]
7. Cloning of full-length methylmalonyl-CoA mutase from a cDNA library using the polymerase chain reaction. Jansen R; Kalousek F; Fenton WA; Rosenberg LE; Ledley FD Genomics; 1989 Feb; 4(2):198-205. PubMed ID: 2567699 [TBL] [Abstract][Full Text] [Related]
8. Analysis of Novel Mutations and Methylmalonyl-CoA Mutase Levels in Thai Patients with Isolated Methylmalonic Acidemia. Sawangareetrakul P; Ketudat Cairns JR; Vatanavicharn N; Liammongkolkul S; Wasant P; Svasti J; Champattanachai V Biochem Genet; 2015 Dec; 53(11-12):310-8. PubMed ID: 26370686 [TBL] [Abstract][Full Text] [Related]
9. Expression and kinetic characterization of methylmalonyl-CoA mutase from patients with the mut- phenotype: evidence for naturally occurring interallelic complementation. Janata J; Kogekar N; Fenton WA Hum Mol Genet; 1997 Sep; 6(9):1457-64. PubMed ID: 9285782 [TBL] [Abstract][Full Text] [Related]
10. Methylmalonyl-CoA mutase induction by cerebral ischemia and neurotoxicity of the mitochondrial toxin methylmalonic acid. Narasimhan P; Sklar R; Murrell M; Swanson RA; Sharp FR J Neurosci; 1996 Nov; 16(22):7336-46. PubMed ID: 8929440 [TBL] [Abstract][Full Text] [Related]
11. Linkage relationships of the human methylmalonyl CoA mutase to the HLA and D6S4 loci on chromosome 6. Zoghbi HY; O'Brien WE; Ledley FD Genomics; 1988 Nov; 3(4):396-8. PubMed ID: 2907507 [TBL] [Abstract][Full Text] [Related]
12. Perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl CoA mutase. Ledley FD Bioessays; 1990 Jul; 12(7):335-40. PubMed ID: 1975493 [TBL] [Abstract][Full Text] [Related]
13. Propionate metabolism in cultured human cells after overexpression of recombinant methylmalonyl CoA mutase: implications for somatic gene therapy. Wilkemeyer M; Stankovics J; Foy T; Ledley FD Somat Cell Mol Genet; 1992 Nov; 18(6):493-505. PubMed ID: 1363155 [TBL] [Abstract][Full Text] [Related]
14. Mutation eliminating mitochondrial leader sequence of methylmalonyl-CoA mutase causes muto methylmalonic acidemia. Ledley FD; Jansen R; Nham SU; Fenton WA; Rosenberg LE Proc Natl Acad Sci U S A; 1990 Apr; 87(8):3147-50. PubMed ID: 1970180 [TBL] [Abstract][Full Text] [Related]
15. [Mutation analysis of the methylmalonyl-CoA mutase gene in ten Mexican patients with methylmalonic acidemia]. Méndez ST; Vela-Amieva M; Velázquez-Arellano A; Ibarra I; Flores ME Rev Invest Clin; 2012; 64(3):255-61. PubMed ID: 23045948 [TBL] [Abstract][Full Text] [Related]
16. Adenoviral-mediated correction of methylmalonyl-CoA mutase deficiency in murine fibroblasts and human hepatocytes. Chandler RJ; Tsai MS; Dorko K; Sloan J; Korson M; Freeman R; Strom S; Venditti CP BMC Med Genet; 2007 Apr; 8():24. PubMed ID: 17470278 [TBL] [Abstract][Full Text] [Related]
17. Towards metabolic sink therapy for mut methylmalonic acidaemia: correction of methylmalonyl-CoA mutase deficiency in T lymphocytes from a mut methylmalonic acidaemia child by retroviral-mediated gene transfer. Chang CC; Hsiao KJ; Lee YM; Lin CM J Inherit Metab Dis; 1999 Oct; 22(7):773-87. PubMed ID: 10518277 [TBL] [Abstract][Full Text] [Related]
18. Cloning and expression of a mutant methylmalonyl coenzyme A mutase with altered cobalamin affinity that causes mut- methylmalonic aciduria. Crane AM; Jansen R; Andrews ER; Ledley FD J Clin Invest; 1992 Feb; 89(2):385-91. PubMed ID: 1346616 [TBL] [Abstract][Full Text] [Related]
19. Molecular analysis and heterologous expression of the gene encoding methylmalonyl-coenzyme A mutase from rifamycin SV-producing strain Amycolatopsis mediterranei U32. Zhang W; Yang L; Jiang W; Zhao G; Yang Y; Chiao J Appl Biochem Biotechnol; 1999 Dec; 82(3):209-25. PubMed ID: 10813025 [TBL] [Abstract][Full Text] [Related]
20. Molecular basis of methylmalonyl-CoA mutase apoenzyme defect in 40 European patients affected by mut(o) and mut- forms of methylmalonic acidemia: identification of 29 novel mutations in the MUT gene. Acquaviva C; Benoist JF; Pereira S; Callebaut I; Koskas T; Porquet D; Elion J Hum Mutat; 2005 Feb; 25(2):167-76. PubMed ID: 15643616 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]