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Journal Abstract Search

100 related items for PubMed ID: 992027

  • 41. Aspartylglucosaminuria in the United States.
    Hreidarsson S, Thomas GH, Valle DL, Stevenson RE, Taylor H, McCarty J, Coker SB, Green WR.
    Clin Genet; 1983 Jun; 23(6):427-35. PubMed ID: 6883788
    [Abstract] [Full Text] [Related]

  • 42. Mutations causing aspartylglucosaminuria (AGU): a lysosomal accumulation disease.
    Ikonen E, Peltonen L.
    Hum Mutat; 1992 Jun; 1(5):361-5. PubMed ID: 1301945
    [Abstract] [Full Text] [Related]

  • 43. Aspartylglucosaminuria in a Canadian family.
    Gordon BA, Rupar CA, Rip JW, Haust MD, Coulter-Mackie MB, Scott E, Hinton GG.
    Clin Invest Med; 1998 Jun; 21(3):114-23. PubMed ID: 9627765
    [Abstract] [Full Text] [Related]

  • 44. Novel mannosidase inhibitor blocking conversion of high mannose to complex oligosaccharides.
    Fuhrmann U, Bause E, Legler G, Ploegh H.
    Nature; 1998 Jun; 307(5953):755-8. PubMed ID: 6230538
    [Abstract] [Full Text] [Related]

  • 45. Spectrum of mutations in aspartylglucosaminuria.
    Ikonen E, Aula P, Grön K, Tollersrud O, Halila R, Manninen T, Syvänen AC, Peltonen L.
    Proc Natl Acad Sci U S A; 1991 Dec 15; 88(24):11222-6. PubMed ID: 1722323
    [Abstract] [Full Text] [Related]

  • 46. [Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway].
    Torp KH, Borud O.
    Tidsskr Nor Laegeforen; 1978 Aug 30; 98(24):1145-6. PubMed ID: 684720
    [No Abstract] [Full Text] [Related]

  • 47. Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samples.
    Aula P, Raivio K, Autio S.
    Pediatr Res; 1976 Jun 30; 10(6):625-9. PubMed ID: 1272639
    [Abstract] [Full Text] [Related]

  • 48. Purification and characterization of a neutral processing mannosidase from calf liver acting on (Man)9(GlcNAc)2 oligosaccharides.
    Schweden J, Legler G, Bause E.
    Eur J Biochem; 1986 Jun 16; 157(3):563-70. PubMed ID: 2941301
    [Abstract] [Full Text] [Related]

  • 49. Regional distribution of glycoasparagine storage material in the brain in aspartylglycosaminuria.
    Maury CP, Haltia M, Palo J.
    J Neurol Sci; 1981 May 16; 50(2):291-8. PubMed ID: 6164750
    [Abstract] [Full Text] [Related]

  • 50. The control of glycoprotein synthesis: N-acetylglucosamine linkage to a mannose residue as a signal for the attachment of L-fucose to the asparagine-linked N-acetylglucosamine residue of glycopeptide from alpha1-acid glycoprotein.
    Wilson JR, Williams D, Schachter H.
    Biochem Biophys Res Commun; 1976 Oct 04; 72(3):909-16. PubMed ID: 985526
    [No Abstract] [Full Text] [Related]

  • 51.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 52. [Contribution of ion exchange chromatography of amino acids to the diagnosis of aspartylglucosaminuria].
    Candito M, Parvy P, Bardet J, Rabier D, Chambon P, Mariani R, Kamoun P.
    Ann Biol Clin (Paris); 1995 Oct 04; 53(3):145-6. PubMed ID: 7574100
    [No Abstract] [Full Text] [Related]

  • 53. Chronic arthritis in patients with aspartylglucosaminuria.
    Arvio MA, Rapola JM, Pelkonen PM.
    J Rheumatol; 1998 Jun 04; 25(6):1131-4. PubMed ID: 9632076
    [Abstract] [Full Text] [Related]

  • 54. The E3-20.5K membrane protein of subgroup B human adenoviruses contains O-linked and complex N-linked oligosaccharides.
    Hawkins LK, Wold WS.
    Virology; 1995 Jul 10; 210(2):335-44. PubMed ID: 7618271
    [Abstract] [Full Text] [Related]

  • 55. Structures of asparagine-linked oligosaccharides of the glycoprotein fetuin having sialic acid linked to N-acetylglucosamine.
    Cumming DA, Hellerqvist CG, Harris-Brandts M, Michnick SW, Carver JP, Bendiak B.
    Biochemistry; 1989 Jul 25; 28(15):6500-12. PubMed ID: 2477057
    [Abstract] [Full Text] [Related]

  • 56. The nature of mannose-containing material which accumulates in cultured fibroblasts from patients with mannosidosis.
    Chester A, Hultberg B, Nordén N E, Szabó L.
    Biochim Biophys Acta; 1980 Feb 07; 627(3):244-9. PubMed ID: 7353055
    [Abstract] [Full Text] [Related]

  • 57. Urinary abnormalities in fucosidosis. Characterization of a disaccharide and two glycoasparagines.
    Lundblad A, Lundsten J, Nordén NE, Sjöblad S, Svensson S, Ockerman PA, Gehlhoff M.
    Eur J Biochem; 1978 Feb 07; 83(2):513-21. PubMed ID: 631132
    [Abstract] [Full Text] [Related]

  • 58. Structural analysis of the major caprine beta-mannosidosis urinary oligosaccharides.
    Matsuura F, Jones MZ, Frazier SE.
    Biochim Biophys Acta; 1983 Aug 23; 759(1-2):67-73. PubMed ID: 6882792
    [Abstract] [Full Text] [Related]

  • 59. Detection of terminal N-linked N-acetylglucosamine residues in the Golgi apparatus using galactosyltransferase and endoglucosaminidase F/peptide N-glycosidase F: adaptation of a biochemical approach to electron microscopy.
    Lucocq JM, Berger EG, Roth J.
    J Histochem Cytochem; 1987 Jan 23; 35(1):67-74. PubMed ID: 2432113
    [Abstract] [Full Text] [Related]

  • 60. The enzymic degradation of ovalbumin and its glycopeptides.
    Conchie J, Hay AJ, Strachan I, Levvy GA.
    Biochem J; 1969 Dec 23; 115(4):717-23. PubMed ID: 5357018
    [Abstract] [Full Text] [Related]

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