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Journal Abstract Search

63 related items for PubMed ID: 1418627

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  • 2. Correction of glycogen storage disease type II by enzyme replacement with a recombinant human acid maltase produced by over-expression in a CHO-DHFR(neg) cell line.
    Martiniuk F, Chen A, Donnabella V, Arvanitopoulos E, Slonim AE, Raben N, Plotz P, Rom WN.
    Biochem Biophys Res Commun; 2000 Oct 05; 276(3):917-23. PubMed ID: 11027569
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  • 4. Production of recombinant human acid α-glucosidase with high-mannose glycans in gnt1 rice for the treatment of Pompe disease.
    Jung JW, Huy NX, Kim HB, Kim NS, Van Giap D, Yang MS.
    J Biotechnol; 2017 May 10; 249():42-50. PubMed ID: 28363873
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  • 7. Production and characterization of recombinant human acid α-glucosidase in transgenic rice cell suspension culture.
    Jung JW, Kim NS, Jang SH, Shin YJ, Yang MS.
    J Biotechnol; 2016 May 20; 226():44-53. PubMed ID: 27050503
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  • 11. cDNA cloning and functional expression of alpha-glucosidase from Mortierella alliacea.
    Tanaka Y, Aki T, Ishihara K, Kawamoto S, Shigeta S, Ono K.
    Appl Microbiol Biotechnol; 2003 Aug 20; 62(2-3):202-9. PubMed ID: 12883865
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  • 12. Recombinant human acid alpha-glucosidase corrects acid alpha-glucosidase-deficient human fibroblasts, quail fibroblasts, and quail myoblasts.
    Yang HW, Kikuchi T, Hagiwara Y, Mizutani M, Chen YT, Van Hove JL.
    Pediatr Res; 1998 Mar 20; 43(3):374-80. PubMed ID: 9505277
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  • 13. Biochemical characterization of Candida albicans alpha-glucosidase I heterologously expressed in Escherichia coli.
    Frade-Pérez MD, Hernández-Cervantes A, Flores-Carreón A, Mora-Montes HM.
    Antonie Van Leeuwenhoek; 2010 Oct 20; 98(3):291-8. PubMed ID: 20358285
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  • 16. Identification of the promoter region and gene expression for human acid alpha glucosidase.
    Tzall S, Martiniuk F.
    Biochem Biophys Res Commun; 1991 May 15; 176(3):1509-15. PubMed ID: 1645546
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  • 17. Correction of glycogen storage disease type II by an adeno-associated virus vector containing a muscle-specific promoter.
    Sun B, Zhang H, Franco LM, Brown T, Bird A, Schneider A, Koeberl DD.
    Mol Ther; 2005 Jun 15; 11(6):889-98. PubMed ID: 15922959
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  • 20. Replacing acid alpha-glucosidase in Pompe disease: recombinant and transgenic enzymes are equipotent, but neither completely clears glycogen from type II muscle fibers.
    Raben N, Fukuda T, Gilbert AL, de Jong D, Thurberg BL, Mattaliano RJ, Meikle P, Hopwood JJ, Nagashima K, Nagaraju K, Plotz PH.
    Mol Ther; 2005 Jan 15; 11(1):48-56. PubMed ID: 15585405
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