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 *

108 related articles for article (PubMed ID: 5032277)

  • 1. Failure of enzymatic induction.
    Applegarth DA; Dunn HG
    N Engl J Med; 1972 Jul; 287(3):148-9. PubMed ID: 5032277
    [No Abstract]   [Full Text] [Related]  

  • 2. Enzymic differentiation between different types of Tay-Sachs disease of similar clinical appearance.
    Clausen J; Melchior JC; Paerregaard P
    Eur Neurol; 1972; 7(1):56-64. PubMed ID: 4336274
    [No Abstract]   [Full Text] [Related]  

  • 3. Gm2-gangliosidosis: studies in cultured fibroblasts.
    Kolodny EH; Milunsky A; Sheng GS
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):130-5. PubMed ID: 4611525
    [No Abstract]   [Full Text] [Related]  

  • 4. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts.
    Hickman S; Shapiro LJ; Neufeld EF
    Biochem Biophys Res Commun; 1974 Mar; 57(1):55-61. PubMed ID: 4364008
    [No Abstract]   [Full Text] [Related]  

  • 5. The correction, in vitro, of lysosomal enzyme deficiencies by means of immunoglobulin-coated liposomes.
    Weissman G; Cohen C; Hoffstein S
    Adv Exp Med Biol; 1976; 68():509-521. PubMed ID: 937118
    [No Abstract]   [Full Text] [Related]  

  • 6. Hexosaminidase C in Tay-Sachs and Sandhoff disease.
    Penton E; Poenaru L; Dreyfus JC
    Biochim Biophys Acta; 1975 May; 391(1):162-9. PubMed ID: 237554
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Tay-Sachs disease: prospects for therapeutic intervention.
    Desnick RJ; Goldberg JD
    Prog Clin Biol Res; 1977; 18():129-41. PubMed ID: 601073
    [No Abstract]   [Full Text] [Related]  

  • 8. Some aspects of the cellular biochemistry of lysosomal and related glycosidases.
    Touster O
    Mol Cell Biochem; 1973 Dec; 2(2):169-77. PubMed ID: 4594433
    [No Abstract]   [Full Text] [Related]  

  • 9. Lysosomes and mental retardation.
    Hirsch I
    Q Rev Biol; 1972 Sep; 47(3):303-12. PubMed ID: 4563310
    [No Abstract]   [Full Text] [Related]  

  • 10. The Tay-Sachs disease fibroblast model: failure to respond to exogenous hexosaminidase A.
    Schneck L; Amsterdam D; Brooks SE; Rosenthal AL; Volk BW
    Pediatrics; 1973 Aug; 52(2):221-6. PubMed ID: 4721444
    [No Abstract]   [Full Text] [Related]  

  • 11. The metabolism of Tay-Sachs ganglioside: catabolic studies with lysosomal enzymes from normal and Tay-Sachs brain tissue.
    Tallman JF; Johnson WG; Brady RO
    J Clin Invest; 1972 Sep; 51(9):2339-45. PubMed ID: 4639018
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Letter: Features of I-cell disease in normal tissues.
    Vladutiu GD
    N Engl J Med; 1976 Jul; 295(2):112-3. PubMed ID: 1272313
    [No Abstract]   [Full Text] [Related]  

  • 13. Disorders of ganglioside metabolism.
    Brady RO; Kolodny EH
    Prog Med Genet; 1972; 8():225-41. PubMed ID: 4336471
    [No Abstract]   [Full Text] [Related]  

  • 14. Tay-Sachs disease: interrelation of hexosaminidases A and B.
    Robinson D; Carroll M
    Lancet; 1972 Feb; 1(7745):322-3. PubMed ID: 4109961
    [No Abstract]   [Full Text] [Related]  

  • 15. Investigations in enzyme replacement therapy in lipid storage diseases.
    Brady RO; Pentchev PG; Gal AG
    Fed Proc; 1975 Apr; 34(5):1310-5. PubMed ID: 804420
    [TBL] [Abstract][Full Text] [Related]  

  • 16. GM2 Type 2--gangliosidosis (Sandhoff's disease)--ocular and pathological manifestations.
    Tremblay M; Szots F
    Can J Ophthalmol; 1974 Jul; 9(3):338-46. PubMed ID: 4276769
    [No Abstract]   [Full Text] [Related]  

  • 17. Multiple human hexosaminidases.
    Sandhoff K
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):214-22. PubMed ID: 4611533
    [No Abstract]   [Full Text] [Related]  

  • 18. Current concepts in genetics. Lysosomal storage diseases.
    Kolodny EH
    N Engl J Med; 1976 May; 294(22):1217-20. PubMed ID: 817200
    [No Abstract]   [Full Text] [Related]  

  • 19. [The activity of various lysosomal acid hydrolases in the normal child. Premise to the biochemical study of cerebral lipidosis].
    Giovannini M; Perego O; Crollari P; Sacchi G; Riva E
    Minerva Pediatr; 1978 Feb; 30(4):339-48. PubMed ID: 25375
    [No Abstract]   [Full Text] [Related]  

  • 20. [Human cerebrospinal fluid hexosaminidases. Activity on N-acetyl-beta-D-glucosaminidic and N-acetyl-beta-galactosaminidic derivatives of 4-methyl-umbelliferone. Evaluation of A and B forms by their thermostability difference].
    Viallard JL; Motta C; Dastugue G
    C R Seances Soc Biol Fil; 1972; 166(12):1704-8. PubMed ID: 4665267
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.