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 *

163 related articles for article (PubMed ID: 269730)

  • 1. Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease.
    Sato K; Imai F; Hatayama I; Roelofs RI
    Biochem Biophys Res Commun; 1977 Sep; 78(2):663-8. PubMed ID: 269730
    [No Abstract]   [Full Text] [Related]  

  • 2. McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
    DiMauro S; Arnold S; Miranda A; Rowland LP
    Trans Am Neurol Assoc; 1977; 102():112-5. PubMed ID: 278321
    [No Abstract]   [Full Text] [Related]  

  • 3. [McArdle's disease (muscular phosphorylase deficiency)].
    Schollmeyer P; Nolte J; Meisel D; Dichgans J; Jerusalem F
    Verh Dtsch Ges Inn Med; 1977 Apr 17-21; 83():1277-80. PubMed ID: 274025
    [No Abstract]   [Full Text] [Related]  

  • 4. McArdle disease: phosphorylase activity in regenerating muscle fibers.
    Mitsumoto H
    Neurology; 1979 Feb; 29(2):258-62. PubMed ID: 285339
    [TBL] [Abstract][Full Text] [Related]  

  • 5. McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme.
    DiMauro S; Arnold S; Miranda A; Rowland LP
    Ann Neurol; 1978 Jan; 3(1):60-6. PubMed ID: 418736
    [TBL] [Abstract][Full Text] [Related]  

  • 6. McArdle's disease: a study on the molecular basis of two different etiologies of myophosphorylase deficiency.
    Koster JF; Slee RG; Jennekens FG; Wintzen AR; van Berkel TJ
    Clin Chim Acta; 1979 Jun; 94(3):229-35. PubMed ID: 111879
    [TBL] [Abstract][Full Text] [Related]  

  • 7. McArdle's disease--what limit to the age of onset?
    Hewlett RH; Gardner-Thorpe C
    S Afr Med J; 1978 Jan; 53(2):60-3. PubMed ID: 273990
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniques.
    Daegelen-Proux D; Kahn A; Marie J; Dreyfus JC
    Ann Hum Genet; 1981 May; 45(2):113-20. PubMed ID: 6797345
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Absence of biochemical heterogeneity in McArdle's disease. A high resolution SDS-polyacrylamide gel electrophoresis study.
    Mantle D; Lauffart B; Atack J; Lane RJ
    J Neurol Sci; 1987 Mar; 78(1):63-70. PubMed ID: 3471865
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Glycogenosis type V of adults: muscle phosphorylase deficiency].
    Coll Cantí J; Illa I; Beleta J; Anglada A; Pradas J; González Sastre F; Grau Veciana JM; Gella FJ
    Med Clin (Barc); 1986 Mar; 86(8):335-8. PubMed ID: 3458989
    [No Abstract]   [Full Text] [Related]  

  • 11. Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.
    Martinuzzi A; Vergani L; Carrozzo R; Fanin M; Bartoloni L; Angelini C; Askanas V; Engel WK
    J Clin Invest; 1993 Oct; 92(4):1774-80. PubMed ID: 8408630
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
    Baqué S; Newgard CB; Gerard RD; Guinovart JJ; Gómez-Foix AM
    Biochem J; 1994 Dec; 304 ( Pt 3)(Pt 3):1009-14. PubMed ID: 7818463
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart.
    Miranda AF; Nette EG; Hartlage PL; DiMauro S
    Neurology; 1979 Nov; 29(11):1538-41. PubMed ID: 291791
    [TBL] [Abstract][Full Text] [Related]  

  • 14. McArdle's & Hers' diseases: glycogen phosphorylase transcriptional expression in human tissues.
    Gorin FA; Mullinax RL; Ignacio PC; Neve RL; Kurnit DM
    J Neurogenet; 1987 Dec; 4(6):293-308. PubMed ID: 3509980
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Myophosphorylase deficiency: two different molecular etiologies.
    Feit H; Brooke MH
    Neurology; 1976 Oct; 26(10):963-7. PubMed ID: 1066528
    [TBL] [Abstract][Full Text] [Related]  

  • 16. McArdle's disease: a nonsense mutation in exon 1 of the muscle glycogen phosphorylase gene explains some but not all cases.
    Bartram C; Edwards RH; Clague J; Beynon RJ
    Hum Mol Genet; 1993 Aug; 2(8):1291-3. PubMed ID: 8401511
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.
    Gautron S; Daegelen D; Mennecier F; Dubocq D; Kahn A; Dreyfus JC
    J Clin Invest; 1987 Jan; 79(1):275-81. PubMed ID: 3466902
    [TBL] [Abstract][Full Text] [Related]  

  • 18. McArdle's disease. The unsolved mystery of the reappearing enzyme.
    Martinuzzi A; Schievano G; Nascimbeni A; Fanin M
    Am J Pathol; 1999 Jun; 154(6):1893-7. PubMed ID: 10362816
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular heterogeneity in McArdle's disease.
    McConchie SM; Coakley J; Edwards RH; Beynon RJ
    Biochim Biophys Acta; 1990 Nov; 1096(1):26-32. PubMed ID: 2268682
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carcinofetal alterations in glycogen phosphorylase isozymes in rat hepatomas.
    Sato K; Sato T; Morris HP; Weinhouse S
    Ann N Y Acad Sci; 1975 Aug; 259():273-86. PubMed ID: 173229
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.