BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

77 related articles for article (PubMed ID: 644316)

  • 21. Myoadenylate deaminase deficiency does not affect muscle anaplerosis during exhaustive exercise in humans.
    Tarnopolsky MA; Parise G; Gibala MJ; Graham TE; Rush JW
    J Physiol; 2001 Jun; 533(Pt 3):881-9. PubMed ID: 11410643
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Clinical heterogeneity and molecular mechanisms in inborn muscle AMP deaminase deficiency.
    Gross M
    J Inherit Metab Dis; 1997 Jun; 20(2):186-92. PubMed ID: 9211191
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Alternative splicing: a mechanism for phenotypic rescue of a common inherited defect.
    Morisaki H; Morisaki T; Newby LK; Holmes EW
    J Clin Invest; 1993 May; 91(5):2275-80. PubMed ID: 8486786
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Isolation and characterization of AMP deaminase from mammalian (rabbit) myocardium.
    Thakkar JK; Janero DR; Yarwood C; Sharif H; Hreniuk D
    Biochem J; 1993 Mar; 290 ( Pt 2)(Pt 2):335-41. PubMed ID: 8452518
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Ergometer exercise in myoadenylate deaminase deficient patients.
    Gross M; Gresser U
    Clin Investig; 1993 Jun; 71(6):461-5. PubMed ID: 8353405
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular biology of AMP deaminase deficiency.
    Gross M
    Pharm World Sci; 1994 Apr; 16(2):55-61. PubMed ID: 8032342
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Disruption of the purine nucleotide cycle. A potential explanation for muscle dysfunction in myoadenylate deaminase deficiency.
    Sabina RL; Swain JL; Patten BM; Ashizawa T; O'Brien WE; Holmes EW
    J Clin Invest; 1980 Dec; 66(6):1419-23. PubMed ID: 7440723
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Exercise-induced pain, stiffness, and tubular aggregation in skeletal muscle.
    Brumback RA; Staton RD; Susag ME
    J Neurol Neurosurg Psychiatry; 1981 Mar; 44(3):250-4. PubMed ID: 7229649
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Pathology of skeletal muscle: principles of reaction patterns and histochemistry and experience with 195 biopsies.
    Manz HJ
    Virchows Arch A Pathol Anat Histol; 1980; 386(1):1-19. PubMed ID: 6996309
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Increased ammonia production during forearm ischemic work test in McArdle's disease.
    Rumpf KW; Wagner H; Kaiser H; Meinck HM; Goebel HH; Scheler F
    Klin Wochenschr; 1981 Dec; 59(23):1319-20. PubMed ID: 6947119
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Myoadenylate deaminase deficiency. Functional and metabolic abnormalities associated with disruption of the purine nucleotide cycle.
    Sabina RL; Swain JL; Olanow CW; Bradley WG; Fishbein WN; DiMauro S; Holmes EW
    J Clin Invest; 1984 Mar; 73(3):720-30. PubMed ID: 6707201
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Diagnostic significance of muscle biopsies in metabolic myopathies. II. Clinical biochemistry].
    Deufel T; Paetzke I; Pongratz D; Hübner G; Wieland OH
    Klin Wochenschr; 1984 Jul; 62(14):651-8. PubMed ID: 6590924
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Histochemical demonstration of differences in AMP deaminase activity in rat skeletal muscle-fibres.
    Meyer RA; Gilloteaux J; Terjung RL
    Experientia; 1980 Jun; 36(6):676-7. PubMed ID: 6448162
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Purine biosynthesis de novo in rat skeletal muscle.
    Sheehan TG; Tully ER
    Biochem J; 1983 Dec; 216(3):605-10. PubMed ID: 6421275
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Fetal congenital lethal hypophosphatasia: histochemical absence of alkaline phosphatase activity in endothelial cells of intramuscular capillaries.
    Goebel HH; Schlie M; Burck U
    Acta Neuropathol; 1982; 57(2-3):236-8. PubMed ID: 6214919
    [No Abstract]   [Full Text] [Related]  

  • 36. Myoadenylate deaminase deficiency in a patient with facial and limb girdle myopathy.
    Mercelis R; Martin JJ; Dehaene I; de Barsy T; Van den Berghe G
    J Neurol; 1981; 225(3):157-66. PubMed ID: 6167680
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Neonatal rotavirus infection.
    Santosham M; Pathak A; Kottapalli S; Vergara J; Wong SJ; Frochlick J; Sack RB
    Lancet; 1982 May; 1(8280):1070-1. PubMed ID: 6122872
    [No Abstract]   [Full Text] [Related]  

  • 38. Myoadenylate deaminase deficiency in twins with recessive olivopontocerebellar atrophy.
    Uziel G; Cornelio F; Gellera C; Perego C; Rimoldi M; DiDonato S
    Ital J Neurol Sci; 1986 Feb; 7(1):107-12. PubMed ID: 3957624
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Deficiency of AMP deaminase in erythrocytes.
    Ogasawara N; Goto H; Yamada Y; Nishigaki I; Itoh T; Hasegawa I; Park KS
    Hum Genet; 1987 Jan; 75(1):15-8. PubMed ID: 3804327
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Myoadenylate deaminase deficiency.
    Goebel HH; Bardosi A; Conrad B; Kuhlendahl HD; DiMauro S; Rumpf KW
    Klin Wochenschr; 1986 Apr; 64(7):342-7. PubMed ID: 3713108
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.