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Journal Abstract Search
228 related items for PubMed ID: 6708943
1. The effects of sucrose loading on lysosomal hydrolases. Kato T, Okada S, Yutaka T, Yabuuchi H. Mol Cell Biochem; 1984; 60(1):83-98. PubMed ID: 6708943 [Abstract] [Full Text] [Related]
2. Normalization of intracellular lysosomal hydrolases in I-cell disease fibroblasts with sucrose loading. Kato T, Okada S, Ohshima T, Inui K, Yutaka T, Yabuuchi H. J Biol Chem; 1982 Jul 10; 257(13):7814-9. PubMed ID: 7085649 [Abstract] [Full Text] [Related]
3. Genetic heterogeneity of I-cell disease is demonstrated by complementation of lysosomal enzyme processing mutants. Shows TB, Mueller OT, Honey NK, Wright CE, Miller AL. Am J Med Genet; 1982 Jul 10; 12(3):343-53. PubMed ID: 6287841 [Abstract] [Full Text] [Related]
4. Lysosomal enzymes in medium from cultured skin fibroblasts from normal individuals and patients with lysosomal diseases. Hultberg B, Sjöblad S. Clin Chim Acta; 1977 Oct 01; 80(1):79-86. PubMed ID: 409577 [Abstract] [Full Text] [Related]
5. Heterogeneity in mucolipidosis II (I-cell disease). Okada S, Kato T, Oshima T, Yutaka T, Yabuuchi H. Clin Genet; 1983 Feb 01; 23(2):155-9. PubMed ID: 6839528 [Abstract] [Full Text] [Related]
6. Induction of beta-galactosidase in beta-galactosidase-alpha-neuraminidase deficiency: effects of leupeptin and sucrose. Kato T, Okada S, Yutaka T, Yabuuchi H. Biochem Int; 1983 Feb 01; 6(2):267-73. PubMed ID: 6433925 [Abstract] [Full Text] [Related]
7. Correction of I-cell defect by hybridization with lysosomal enzyme deficient human fibroblasts. d'Azzo A, Halley DJ, Hoogeveen A, Galjaard H. Am J Hum Genet; 1980 Jul 01; 32(4):519-28. PubMed ID: 6772024 [Abstract] [Full Text] [Related]
8. The role of lysosomal enzymes in killing of mammalian cells by the lysosomotropic detergent N-dodecylimidazole. Wilson PD, Firestone RA, Lenard J. J Cell Biol; 1987 May 01; 104(5):1223-9. PubMed ID: 3571330 [Abstract] [Full Text] [Related]
9. Biochemical studies on lymphoblastoid cells with inherited N-acetyl-glucosamine 1-phosphotransferase deficiency (I-cell disease). Okada S, Handa M, Hashimoto T, Nishimoto J, Inui K, Furukawa M, Furuyama J, Yabuuchi H, Tate M, Gasa S. Biochem Int; 1988 Aug 01; 17(2):375-83. PubMed ID: 2847740 [Abstract] [Full Text] [Related]
10. Preferential inhibition of lysosomal beta-mannosidase by sucrose. McCabe NR, Biliter W, Dawson G. Enzyme; 1990 Aug 01; 43(3):137-45. PubMed ID: 2095335 [Abstract] [Full Text] [Related]
11. Biochemical heterogeneity in I-cell disease. Sucrose-loading test classifies two distinct subtypes. Okada S, Inui K, Furukawa M, Midorikawa M, Nishimoto J, Yabuuchi H, Kato T, Watanabe M, Gasa S, Makita A. Enzyme; 1987 Aug 01; 38(1-4):267-72. PubMed ID: 2831041 [Abstract] [Full Text] [Related]
12. Properties of N-acetyl-beta-D-hexosaminidase from isolated normal and I-cell lysosomes. Miller AL, Kress BC, Stein R, Kinnon C, Kern H, Schneider JA, Harms E. J Biol Chem; 1981 Sep 10; 256(17):9352-62. PubMed ID: 7263719 [Abstract] [Full Text] [Related]
13. The mucolipidoses: identification by abnormal electrophoretic patterns of lysosomal hydrolases. Honey NK, Miller AL, Shows TB. Am J Med Genet; 1981 Sep 10; 9(3):239-53. PubMed ID: 7282783 [Abstract] [Full Text] [Related]
14. Effect on lysosomes of invertase endocytosed by rat-liver. Jadot M, Wattiaux-De Coninck S, Wattiaux R. Eur J Biochem; 1985 Sep 16; 151(3):485-8. PubMed ID: 4029143 [Abstract] [Full Text] [Related]
19. [Intracellular activity and secretion of various lysosomal glycosidases in cultured human skin fibroblasts]. Ivleva TS, Beliaeva ID, Vidershaĭn GIa. Biokhimiia; 1986 Jul 16; 51(7):1150-5. PubMed ID: 2942192 [Abstract] [Full Text] [Related]
20. 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 16; 3(4):313-8. PubMed ID: 8400547 [Abstract] [Full Text] [Related] Page: [Next] [New Search]