These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 518612)

  • 1. beta-Galactosidase deficient-type mucolipidosis: a complementation study of neuraminidase in somatic cell hybrids.
    Kato T; Okada S; Yutaka T; Inui K; Yabuuchi H; Chiyo H; Furuyama JI; Okada Y
    Biochem Biophys Res Commun; 1979 Nov; 91(1):114-7. PubMed ID: 518612
    [No Abstract]   [Full Text] [Related]  

  • 2. Human beta-galactosidase and alpha-neuraminidase deficient mucolipidosis: genetic complementation analysis of the neuraminidase deficiency.
    Mueller OT; Shows TB
    Hum Genet; 1982; 60(2):158-62. PubMed ID: 7076257
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The complementation of beta-galactosidase in fused cells of mucolipidosis II with another variants of beta-galactosidase deficiency using new single cell enzyme assay.
    Okada S; Kato T; Yabuuchi H; Okada Y
    Biochem Biophys Res Commun; 1979 May; 88(2):559-62. PubMed ID: 111672
    [No Abstract]   [Full Text] [Related]  

  • 4. Oligosaccharide and ganglioside neuraminidase activities of mucolipidosis I (sialidosis) and mucolipidosis II (I-cell disease) fibroblasts.
    Cantz M; Messer H
    Eur J Biochem; 1979 Jun; 97(1):113-8. PubMed ID: 477659
    [No Abstract]   [Full Text] [Related]  

  • 5. Genetic heterogeneity in human neuraminidase deficiency.
    Hoogeveen AT; Verheijen FW; d'Azzo A; Galjaard H
    Nature; 1980 Jun; 285(5765):500-2. PubMed ID: 6772959
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adult mucolipidosis with beta-galactosidase and neuraminidase deficiencies.
    Kuriyama M; Okada S; Tanaka Y; Umezaki H
    J Neurol Sci; 1980 May; 46(2):245-54. PubMed ID: 6770051
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Adult type GMl-gangliosidosis: a complementation study on somatic cell hybrids.
    Suzuki Y; Furukawa T; Hoogeveen A; Verheijen F; Galjaard H
    Brain Dev; 1979; 1(2):83-6. PubMed ID: 121869
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 32(4):519-28. PubMed ID: 6772024
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Studies on sialidosis and mucolipidosis. Properties of neuraminidase in cultured skin fibroblasts].
    Beauregard G; Melançon SB; Dallaire L; Potier M
    Biochim Biophys Acta; 1982 Sep; 706(2):212-20. PubMed ID: 7126599
    [No Abstract]   [Full Text] [Related]  

  • 10. Sialidosis and galactosialidosis: chromosomal assignment of two genes associated with neuraminidase-deficiency disorders.
    Mueller OT; Henry WM; Haley LL; Byers MG; Eddy RL; Shows TB
    Proc Natl Acad Sci U S A; 1986 Mar; 83(6):1817-21. PubMed ID: 3081902
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Interspecific genetic complementation analysis of human and sheep fibroblasts with beta-galactosidase deficiency.
    Ahern-Rindell AJ; Murnane RD; Prieur DJ
    Somat Cell Mol Genet; 1989 Nov; 15(6):525-33. PubMed ID: 2512653
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Neuraminidase in mucolipidoses: normal activity in frozen autopsy tissues from three patients with I-cell disease and adult beta-galactosidase deficiency.
    Suzuki Y; Fukuoka K
    Clin Chim Acta; 1979 Dec; 99(2):107-12. PubMed ID: 116781
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Km defect in neuraminidase of dysmorphic type sialidosis with and without beta-galactosidase deficiency.
    Ben-Yoseph Y; Momoi T; Baylerian MS; Nadler HL
    Clin Chim Acta; 1982 Aug; 123(3):233-40. PubMed ID: 6811161
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Correction of human mucolipidosis II enzyme abnormalities in somatic cell hybrids.
    Champion MJ; Shows TB
    Nature; 1977 Nov; 270(5632):64-6. PubMed ID: 562989
    [No Abstract]   [Full Text] [Related]  

  • 15. Fusion with enucleated fibroblasts corrects "I-cell" defect.
    D'Azzo A; Konings A; Verkerk A; Jongkind JF; Galjaard H
    Exp Cell Res; 1980 Jun; 127(2):484-7. PubMed ID: 6769689
    [No Abstract]   [Full Text] [Related]  

  • 16. Neuraminidase activity in liver and brain from patients with I-cell disease.
    Minami R; Kudoh T; Oyanagi K; Nakao T
    Clin Chim Acta; 1979 Aug; 96(1-2):107-11. PubMed ID: 113136
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Intergenic complementation after fusion of fibroblasts from different patients with beta-galactosidase deficiency.
    Hoeksema HL; van Diggelen OP; Galjaard H
    Biochim Biophys Acta; 1979 Jan; 566(1):72-9. PubMed ID: 103586
    [No Abstract]   [Full Text] [Related]  

  • 18. A case of neuraminidase deficiency associated with a partial beta-galactosidase defect. Clinical, biochemical and radiological studies.
    Okada S; Yutaka T; Kato T; Ikehara C; Yabuuchi H; Okawa M; Inui M; Chiyo H
    Eur J Pediatr; 1979 Apr; 130(4):239-49. PubMed ID: 436849
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 12(3):343-53. PubMed ID: 6287841
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Adult type mucolipidosis with beta-galactosidase and sialidase deficiency. Histological and biochemical studies.
    Kobayashi T; Ohta M; Goto I; Tanaka Y; Kuroiwa Y
    J Neurol; 1979 Sep; 221(3):137-49. PubMed ID: 91667
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.