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139 related items for PubMed ID: 1822239

  • 1. Biosynthesis, processing, and secretion of alpha-L-fucosidase in lymphoid cells from patients with I-cell disease and pseudo-Hurler polydystrophy.
    DiCioccio RA, Miller AL.
    Glycobiology; 1991 Dec; 1(6):595-604. PubMed ID: 1822239
    [Abstract] [Full Text] [Related]

  • 2. Phosphorylation and subcellular location of alpha-L-fucosidase in lymphoid cells from patients with I-cell disease and pseudo-Hurler polydystrophy.
    DiCioccio RA, Miller AL.
    Glycobiology; 1993 Oct; 3(5):489-95. PubMed ID: 8286862
    [Abstract] [Full Text] [Related]

  • 3. Biosynthesis, processing, and extracellular release of alpha-L-fucosidase in lymphoid cell lines of different genetic origins.
    DiCioccio RA, Brown KS.
    Biochem Genet; 1988 Jun; 26(5-6):401-20. PubMed ID: 3265056
    [Abstract] [Full Text] [Related]

  • 4. Defective expression of alpha-L-fucosidase by lymphoid cells of a fucosidosis patient.
    DiCioccio RA, Gordon BA.
    Clin Biochem; 1991 Jun; 24(3):265-70. PubMed ID: 1873910
    [Abstract] [Full Text] [Related]

  • 5. Abnormal expression of alpha-L-fucosidase in lymphoid cell lines of fucosidosis patients.
    DiCioccio RA, Darby JK, Willems PJ.
    Biochem Genet; 1989 Jun; 27(5-6):279-90. PubMed ID: 2803224
    [Abstract] [Full Text] [Related]

  • 6. Binding receptors for alpha-L-fucosidase in human B-lymphoid cell lines.
    Dicioccio RA, Miller AL.
    Glycoconj J; 1992 Feb; 9(1):56-62. PubMed ID: 1327338
    [Abstract] [Full Text] [Related]

  • 7. Effect of glycosylation inhibitors and acidotropic amines on the synthesis, processing, and intracellular-extracellular distribution of alpha-L-fucosidase in B-lymphoblastoid cells.
    DiCioccio RA, Mahoney CM.
    Carbohydr Res; 1990 Mar 25; 197():217-26. PubMed ID: 2140711
    [Abstract] [Full Text] [Related]

  • 8. Fibroblasts from patients with I-cell disease and pseudo-Hurler polydystrophy are deficient in uridine 5'-diphosphate-N-acetylglucosamine: glycoprotein N-acetylglucosaminylphosphotransferase activity.
    Reitman ML, Varki A, Kornfeld S.
    J Clin Invest; 1981 May 25; 67(5):1574-9. PubMed ID: 6262380
    [Abstract] [Full Text] [Related]

  • 9. Identification of a variant of mucolipidosis III (pseudo-Hurler polydystrophy): a catalytically active N-acetylglucosaminylphosphotransferase that fails to phosphorylate lysosomal enzymes.
    Varki AP, Reitman ML, Kornfeld S.
    Proc Natl Acad Sci U S A; 1981 Dec 25; 78(12):7773-7. PubMed ID: 6461005
    [Abstract] [Full Text] [Related]

  • 10. Lack of proteolytic processing of alpha-L-fucosidase in human skin fibroblasts.
    Leibold DM, Robinson CB, Scanlin TF, Glick MC.
    J Cell Physiol; 1988 Dec 25; 137(3):411-20. PubMed ID: 3192622
    [Abstract] [Full Text] [Related]

  • 11. Light and heavy lysosomes: characterization of N-acetyl-beta-D-hexosaminidase isolated from normal and I-cell disease lymphoblasts.
    Miller AL, Norton V, Robertson R, Jenks M, Yeh RY, Wright D.
    Glycobiology; 1993 Aug 25; 3(4):313-8. PubMed ID: 8400547
    [Abstract] [Full Text] [Related]

  • 12. Altered molecular size of N-acetylglucosamine 1-phosphotransferase in I-cell disease and pseudo-Hurler polydystrophy.
    Ben-Yoseph Y, Potier M, Mitchell DA, Pack BA, Melançon SB, Nadler HL.
    Biochem J; 1987 Dec 15; 248(3):697-701. PubMed ID: 2829837
    [Abstract] [Full Text] [Related]

  • 13. Synthesis and processing of rat sperm-associated alpha-L-fucosidase.
    Hancock LW, Raab LS, Aronson NN.
    Biol Reprod; 1993 Jun 15; 48(6):1228-38. PubMed ID: 8318578
    [Abstract] [Full Text] [Related]

  • 14. Synthesis and processing of lysosomal alpha-fucosidase in cultured human fibroblasts.
    Johnson KF, Hancock LW, Dawson G.
    Biochim Biophys Acta; 1991 Jan 23; 1073(1):120-8. PubMed ID: 1899340
    [Abstract] [Full Text] [Related]

  • 15. Metabolic correction of fucosidosis lymphoid cells by galaptin-alpha-L-fucosidase conjugates.
    Allen HJ, Ahmed H, DiCioccio RA.
    Biochem Biophys Res Commun; 1990 Oct 15; 172(1):335-40. PubMed ID: 2222477
    [Abstract] [Full Text] [Related]

  • 16. Characterization of the mannose 6-phosphate-dependent pathway of lysosomal enzyme routing in an invertebrate.
    Alvarez V, Parodi AJ, Couso R.
    Biochem J; 1995 Sep 01; 310 ( Pt 2)(Pt 2):589-95. PubMed ID: 7654199
    [Abstract] [Full Text] [Related]

  • 17. Characterization of the mutant N-acetylglucosaminylphosphotransferase in I-cell disease and pseudo-Hurler polydystrophy: complementation analysis and kinetic studies.
    Ben-Yoseph Y, Pack BA, Mitchell DA, Elwell DG, Potier M, Melançon SB, Nadler HL.
    Enzyme; 1986 Sep 01; 35(2):106-16. PubMed ID: 3017692
    [Abstract] [Full Text] [Related]

  • 18. Steps in the phosphorylation of the high mannose oligosaccharides of lysosomal enzymes.
    Kornfeld S, Reitman ML, Varki A, Goldberg D, Gabel CA.
    Ciba Found Symp; 1982 Sep 01; (92):138-56. PubMed ID: 6295719
    [Abstract] [Full Text] [Related]

  • 19. Molecular defect in processing alpha-fucosidase in fucosidosis.
    Johnson K, Dawson G.
    Biochem Biophys Res Commun; 1985 Nov 27; 133(1):90-7. PubMed ID: 4074382
    [Abstract] [Full Text] [Related]

  • 20. Effect of tunicamycin and cycloheximide on the secretion of acid hydrolases from I-cell cultured fibroblasts.
    Miller AL, Kress BC, Lewis L, Stein R, Kinnon C.
    Biochem J; 1980 Mar 15; 186(3):971-5. PubMed ID: 7396846
    [Abstract] [Full Text] [Related]

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