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Journal Abstract Search


81 related items for PubMed ID: 1912068

  • 21. Cathepsin A/protective protein: an unusual lysosomal multifunctional protein.
    Hiraiwa M.
    Cell Mol Life Sci; 1999 Dec; 56(11-12):894-907. PubMed ID: 11212324
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  • 22. New mutations in the PPBG gene lead to loss of PPCA protein which affects the level of the beta-galactosidase/neuraminidase complex and the EBP-receptor.
    Malvagia S, Morrone A, Caciotti A, Bardelli T, d'Azzo A, Ancora G, Zammarchi E, Donati MA.
    Mol Genet Metab; 2004 May; 82(1):48-55. PubMed ID: 15110321
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  • 23. Structure of the lysosomal neuraminidase-beta-galactosidase-carboxypeptidase multienzymic complex.
    Potier M, Michaud L, Tranchemontagne J, Thauvette L.
    Biochem J; 1990 Apr 01; 267(1):197-202. PubMed ID: 2109603
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  • 25. Association of N-acetylgalactosamine-6-sulfate sulfatase with the multienzyme lysosomal complex of beta-galactosidase, cathepsin A, and neuraminidase. Possible implication for intralysosomal catabolism of keratan sulfate.
    Pshezhetsky AV, Potier M.
    J Biol Chem; 1996 Nov 08; 271(45):28359-65. PubMed ID: 8910459
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  • 30. Characterization of beta-galactosidase mutations Asp332-->Asn and Arg148-->Ser, and a polymorphism, Ser532-->Gly, in a case of GM1 gangliosidosis.
    Zhang S, Bagshaw R, Hilson W, Oho Y, Hinek A, Clarke JT, Callahan JW.
    Biochem J; 2000 Jun 15; 348 Pt 3(Pt 3):621-32. PubMed ID: 10839995
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  • 31. [Active centers of gamma-glutamyltransferase in the aerosol OT reverse micellar system in octane by an inhibitor analysis method].
    Nametkin SI, Kabanov AV, Levashov AV.
    Bioorg Khim; 1991 Aug 15; 17(8):1027-32. PubMed ID: 1721511
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  • 32. Role of beta-galactosidase and elastin binding protein in lysosomal and nonlysosomal complexes of patients with GM1-gangliosidosis.
    Caciotti A, Donati MA, Boneh A, d'Azzo A, Federico A, Parini R, Antuzzi D, Bardelli T, Nosi D, Kimonis V, Zammarchi E, Morrone A.
    Hum Mutat; 2005 Mar 15; 25(3):285-92. PubMed ID: 15714521
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  • 33. [Angiotensin-converting enzyme in an OAT-octane reversed micelle system: interaction with the matrix].
    Kost OA, Ort TA, Nikol'skaia II, Nametkin SN, Levashov AV.
    Bioorg Khim; 1995 Jun 15; 21(6):403-7. PubMed ID: 7544974
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  • 35. Identification and in vitro reconstitution of lysosomal neuraminidase from human placenta.
    van der Horst GT, Galjart NJ, d'Azzo A, Galjaard H, Verheijen FW.
    J Biol Chem; 1989 Jan 15; 264(2):1317-22. PubMed ID: 2492018
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  • 36. Inactivation of GM1-ganglioside beta-galactosidase by a specific inhibitor: a model for ganglioside storage disease.
    Singer HS, Tiemeyer M, Slesinger PA, Sinnott ML.
    Ann Neurol; 1987 May 15; 21(5):497-503. PubMed ID: 3035998
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  • 38. Inherited lysosomal storage disease associated with deficiencies of beta-galactosidase and alpha-neuraminidase in sheep.
    Ahern-Rindell AJ, Prieur DJ, Murnane RD, Raghavan SS, Daniel PF, McCluer RH, Walkley SU, Parish SM.
    Am J Med Genet; 1988 Sep 15; 31(1):39-56. PubMed ID: 3146925
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  • 40. [Enzymes incorporated into reversed micelles of surfactants in organic solvents. Study of the protein-aerosol OT-H2O-octane system by sedimentation analysis].
    Khmel'nitskiĭ IuL, Levashov AV, Kliachko NL, Cherniak VIa, Martinek K.
    Biokhimiia; 1982 Jan 15; 47(1):86-99. PubMed ID: 6175348
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