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Journal Abstract Search
110 related items for PubMed ID: 3318108
1. [Characteristics of biogenesis and substrate specificity of lysosomal glycosidases under normal conditions and in glycosidoses]. Vidershaĭn GIa. Vopr Med Khim; 1987; 33(5):24-33. PubMed ID: 3318108 [Abstract] [Full Text] [Related]
2. [Lysosomal glycosidases and glycoproteinoses]. Montreuil J. C R Seances Soc Biol Fil; 1981; 175(5):694-707. PubMed ID: 6456795 [Abstract] [Full Text] [Related]
10. 4-Trifluoromethylumbelliferyl glycosides as new substrates for revealing diseases connected with hereditary deficiency of lysosome glycosidases. Karpova EA, Voznyi YaV, Dudukina TV, Tsvetkova IV. Biochem Int; 1991 Aug; 24(6):1135-44. PubMed ID: 1781792 [Abstract] [Full Text] [Related]
11. Several cooperating binding sites mediate the interaction of a lysosomal enzyme with phosphotransferase. Tikkanen R, Peltola M, Oinonen C, Rouvinen J, Peltonen L. EMBO J; 1997 Nov 17; 16(22):6684-93. PubMed ID: 9362483 [Abstract] [Full Text] [Related]
13. [Design of fluorogenic substrates of lysosomal hydrolases and their use in the study and diagnosis of hereditary enzyme defects]. Tsvetkova IV. Vestn Ross Akad Med Nauk; 1995 Nov 17; (2):52-6. PubMed ID: 7756932 [Abstract] [Full Text] [Related]
17. [Glycosidases of various mollusks: general properties, kinetic studies and action on natural substrates]. Cabezas JA, Calvo P, Díez T, Melgar MJ, Ortíz de la Tabla MV, de Pedro A, Pérez N, Reglero A, Santamaría MG, Villar E. Rev Esp Fisiol; 1982 Nov 17; 38 Suppl():73-9. PubMed ID: 6293019 [Abstract] [Full Text] [Related]
19. Lysosomal enzymuria is a feature of hereditary Fanconi syndrome and is related to elevated CI-mannose-6-P-receptor excretion. Norden AG, Gardner SC, Van't Hoff W, Unwin RJ. Nephrol Dial Transplant; 2008 Sep 17; 23(9):2795-803. PubMed ID: 18174267 [Abstract] [Full Text] [Related]