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Journal Abstract Search

226 related items for PubMed ID: 19884343

  • 1. Impaired lysosomal trimming of N-linked oligosaccharides leads to hyperglycosylation of native lysosomal proteins in mice with alpha-mannosidosis.
    Damme M, Morelle W, Schmidt B, Andersson C, Fogh J, Michalski JC, Lübke T.
    Mol Cell Biol; 2010 Jan; 30(1):273-83. PubMed ID: 19884343
    [Abstract] [Full Text] [Related]

  • 2. Efficacy of enzyme replacement therapy in alpha-mannosidosis mice: a preclinical animal study.
    Roces DP, Lüllmann-Rauch R, Peng J, Balducci C, Andersson C, Tollersrud O, Fogh J, Orlacchio A, Beccari T, Saftig P, von Figura K.
    Hum Mol Genet; 2004 Sep 15; 13(18):1979-88. PubMed ID: 15269179
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  • 3. Lysosomal alpha-mannosidase and alpha-mannosidosis.
    Paciotti S, Codini M, Tasegian A, Ceccarini MR, Cataldi S, Arcuri C, Fioretti B, Albi E, Beccari T.
    Front Biosci (Landmark Ed); 2017 Jan 01; 22(1):157-167. PubMed ID: 27814608
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  • 4. Enzyme replacement therapy in alpha-mannosidosis guinea-pigs.
    Crawley AC, King B, Berg T, Meikle PJ, Hopwood JJ.
    Mol Genet Metab; 2006 Jan 01; 89(1-2):48-57. PubMed ID: 16807033
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  • 5. Targeted disruption of the lysosomal alpha-mannosidase gene results in mice resembling a mild form of human alpha-mannosidosis.
    Stinchi S, Lüllmann-Rauch R, Hartmann D, Coenen R, Beccari T, Orlacchio A, von Figura K, Saftig P.
    Hum Mol Genet; 1999 Aug 01; 8(8):1365-72. PubMed ID: 10400983
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  • 6. Reversal of peripheral and central neural storage and ataxia after recombinant enzyme replacement therapy in alpha-mannosidosis mice.
    Blanz J, Stroobants S, Lüllmann-Rauch R, Morelle W, Lüdemann M, D'Hooge R, Reuterwall H, Michalski JC, Fogh J, Andersson C, Saftig P.
    Hum Mol Genet; 2008 Nov 15; 17(22):3437-45. PubMed ID: 18713755
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  • 7. Alpha-Mannosidosis: Therapeutic Strategies.
    Ceccarini MR, Codini M, Conte C, Patria F, Cataldi S, Bertelli M, Albi E, Beccari T.
    Int J Mol Sci; 2018 May 17; 19(5):. PubMed ID: 29772816
    [Abstract] [Full Text] [Related]

  • 8. Direct enzyme transfer from lymphocytes corrects a lysosomal storage disease.
    Abraham D, Muir H, Olsen I, Winchester B.
    Biochem Biophys Res Commun; 1985 Jun 14; 129(2):417-25. PubMed ID: 4015639
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  • 12. A human lysosomal alpha(1----6)-mannosidase active on the branched trimannosyl core of complex glycans.
    Daniel PF, Evans JE, De Gasperi R, Winchester B, Warren CD.
    Glycobiology; 1992 Aug 14; 2(4):327-36. PubMed ID: 1421754
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  • 15. The catabolism of mammalian glycoproteins. Comparison of the storage products in bovine, feline and human mannosidosis.
    Abraham D, Blakemore WF, Jolly RD, Sidebotham R, Winchester B.
    Biochem J; 1983 Dec 01; 215(3):573-9. PubMed ID: 6661184
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  • 17. A human lysosomal alpha-mannosidase specific for the core of complex glycans.
    De Gasperi R, Daniel PF, Warren CD.
    J Biol Chem; 1992 May 15; 267(14):9706-12. PubMed ID: 1577805
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  • 18. Purification and characterization of recombinant human lysosomal alpha-mannosidase.
    Berg T, King B, Meikle PJ, Nilssen Ø, Tollersrud OK, Hopwood JJ.
    Mol Genet Metab; 2001 May 15; 73(1):18-29. PubMed ID: 11350179
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  • 19. The Application of HPLC-FLD and NMR in the Monitoring of Therapy Efficacy in Alpha-Mannosidosis.
    Krchňák M, Kodríková R, Matulová M, Nemčovič M, Uhliariková I, Katrlík J, Šalingová A, Hlavatá A, Juríčková K, Baráth P, Mucha J, Pakanová Z.
    Front Biosci (Landmark Ed); 2023 Feb 28; 28(2):39. PubMed ID: 36866557
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