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Journal Abstract Search

159 related items for PubMed ID: 1363156

  • 1. 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
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  • 2. 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 30; 8():24. PubMed ID: 17470278
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  • 4. Molecular cloning of L-methylmalonyl-CoA mutase: gene transfer and analysis of mut cell lines.
    Ledley FD, Lumetta M, Nguyen PN, Kolhouse JF, Allen RH.
    Proc Natl Acad Sci U S A; 1988 May 30; 85(10):3518-21. PubMed ID: 2453061
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  • 6. Perspectives on methylmalonic acidemia resulting from molecular cloning of methylmalonyl CoA mutase.
    Ledley FD.
    Bioessays; 1990 Jul 30; 12(7):335-40. PubMed ID: 1975493
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  • 7. 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 30; 87(3):915-8. PubMed ID: 1671869
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  • 11. Identification of two novel mutations in the methylmalonyl-CoA mutase gene with decreased levels of mutant mRNA in methylmalonic acidemia.
    Ogasawara M, Matsubara Y, Mikami H, Narisawa K.
    Hum Mol Genet; 1994 Jun 30; 3(6):867-72. PubMed ID: 7951229
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  • 15. 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 30; 87(8):3147-50. PubMed ID: 1970180
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  • 16. Liver-directed recombinant adeno-associated viral gene delivery rescues a lethal mouse model of methylmalonic acidemia and provides long-term phenotypic correction.
    Carrillo-Carrasco N, Chandler RJ, Chandrasekaran S, Venditti CP.
    Hum Gene Ther; 2010 Sep 30; 21(9):1147-54. PubMed ID: 20486773
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  • 17. Molecular analysis of methylmalonyl-CoA mutase deficiency: identification of three missense mutations in mut0 patients.
    Mikami H, Ogasawara M, Matsubara Y, Kikuchi M, Miyabayashi S, Kure S, Narisawa K.
    J Hum Genet; 1999 Sep 30; 44(1):35-9. PubMed ID: 9929975
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  • 18. Heterogeneous alleles and expression of methylmalonyl CoA mutase in mut methylmalonic acidemia.
    Ledley FD, Crane AM, Lumetta M.
    Am J Hum Genet; 1990 Mar 30; 46(3):539-47. PubMed ID: 1968706
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  • 19. Heterozygous mutations at the mut locus in fibroblasts with mut0 methylmalonic acidemia identified by polymerase-chain-reaction cDNA cloning.
    Jansen R, Ledley FD.
    Am J Hum Genet; 1990 Nov 30; 47(5):808-14. PubMed ID: 1977311
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  • 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 30; 25(2):167-76. PubMed ID: 15643616
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