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Journal Abstract Search

235 related items for PubMed ID: 10518277

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  • 3. 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. Adenovirus-mediated gene delivery rescues a neonatal lethal murine model of mut(0) methylmalonic acidemia.
    Chandler RJ, Venditti CP.
    Hum Gene Ther; 2008 Jan 30; 19(1):53-60. PubMed ID: 18052792
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  • 5. 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 30; 18(6):507-16. PubMed ID: 1363156
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  • 6. 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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  • 7. 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 30; 18(6):493-505. PubMed ID: 1363155
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  • 12. 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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  • 15. Molecular, biochemical, and structural analysis of a novel mutation in patients with methylmalonyl-CoA mutase deficiency.
    Keyfi F, Sankian M, Moghaddassian M, Rolfs A, Varasteh AR.
    Gene; 2016 Jan 15; 576(1 Pt 2):208-13. PubMed ID: 26449400
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  • 17. Mutation and biochemical analysis of 19 probands with mut0 and 13 with mut- methylmalonic aciduria: identification of seven novel mutations.
    Lempp TJ, Suormala T, Siegenthaler R, Baumgartner ER, Fowler B, Steinmann B, Baumgartner MR.
    Mol Genet Metab; 2007 Mar 15; 90(3):284-90. PubMed ID: 17113806
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  • 19. Correction of methylmalonic aciduria in vivo using a codon-optimized lentiviral vector.
    Wong ES, McIntyre C, Peters HL, Ranieri E, Anson DS, Fletcher JM.
    Hum Gene Ther; 2014 Jun 15; 25(6):529-38. PubMed ID: 24568291
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