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Journal Abstract Search

121 related items for PubMed ID: 1917896

  • 1. Isolation and characterization of major urinary oligosaccharides excreted by a patient with type 3 GM1 gangliosidosis.
    Tsuji S, Ariga T, Ando S, Tanaka Y, Kon K, Yahagi T, Ohta K, Miyatake T.
    J Biochem; 1991 May; 109(5):722-7. PubMed ID: 1917896
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  • 4. Characterization of a novel type of chain-terminator Gal beta 1-6Gal beta 1-4)GlcNAc in an oligosaccharide related to N-glycosylated protein glycans isolated from GM1 the urine of patients with gangliosidosis.
    Michalski JC, Lemoine J, Wieruszeski JM, Fournet B, Montreuil J, Strecker G.
    Eur J Biochem; 1991 Jun 01; 198(2):521-6. PubMed ID: 1904026
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  • 5. Urinary oligosaccharides of GM1-gangliosidosis. Different excretion patterns of oligosaccharides in the urine of type 1 and type 2 subgroups.
    Yamashita K, Ohkura T, Okada S, Yabuuchi H, Kobata A.
    J Biol Chem; 1981 May 25; 256(10):4789-98. PubMed ID: 6785275
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  • 7. Structure of seven oligosaccharides excreted in the urine of a patient with Sandhoff's disease (GM2 gangliosidosis-variant O).
    Strecker G, Herlant-Peers MC, Fournet B, Montreul J.
    Eur J Biochem; 1977 Nov 15; 81(1):165-71. PubMed ID: 412673
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  • 10. Diagnosis of subtypes of GM1 gangliosidosis in vitro and in vivo--using urinary oligosaccharides as substrates.
    Takahashi Y, Orii T.
    Clin Chim Acta; 1989 Feb 22; 179(3):219-27. PubMed ID: 2496942
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  • 15. Structure of two sulphated oligosaccharides from respiratory mucins of a patient suffering from cystic fibrosis. A fast-atom-bombardment m.s. and 1H-n.m.r. spectroscopic study.
    Lamblin G, Rahmoune H, Wieruszeski JM, Lhermitte M, Strecker G, Roussel P.
    Biochem J; 1991 Apr 01; 275 ( Pt 1)(Pt 1):199-206. PubMed ID: 2018475
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  • 17. Primary structure of a trisialylated oligosaccharide from human milk.
    Fievre S, Wieruszeski JM, Michalski JC, Lemoine J, Montreuil J, Strecker G.
    Biochem Biophys Res Commun; 1991 Jun 14; 177(2):720-5. PubMed ID: 2049094
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  • 18. The simple detection of neuraminic acid-containing urinary oligosaccharides in patients with glycoprotein storage diseases.
    Sewell AC.
    J Inherit Metab Dis; 1983 Jun 14; 6(4):153-7. PubMed ID: 6422155
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