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157 related items for PubMed ID: 1203056

  • 21. Mapping of the gene for X-linked liver glycogenosis due to phosphorylase kinase deficiency to human chromosome region Xp22.
    Willems PJ, Hendrickx J, Van der Auwera BJ, Vits L, Raeymaekers P, Coucke PJ, Van den Bergh I, Berger R, Smit GP, Van Broeckhoven C.
    Genomics; 1991 Apr; 9(4):565-9. PubMed ID: 1674721
    [Abstract] [Full Text] [Related]

  • 22. Mammalian skeletal muscle myosin light chain kinases. A comparison by antiserum cross-reactivity.
    Nunnally MH, Stull JT.
    J Biol Chem; 1984 Feb 10; 259(3):1776-80. PubMed ID: 6546381
    [Abstract] [Full Text] [Related]

  • 23. Skeletal muscle glycogen content, structure, and metabolism are normal in rats with hepatic glycogen phosphorylase kinase deficiency.
    Calder PC, Geddes R.
    Biochem Int; 1989 Dec 10; 19(6):1231-9. PubMed ID: 2635861
    [Abstract] [Full Text] [Related]

  • 24. Monoclonal antibodies to rabbit skeletal muscle phosphorylase kinase. Probes for studies of subunit function.
    Hessová Z, Thieleczek R, Varsányi M, Falkenberg FW, Heilmeyer LM.
    J Biol Chem; 1985 Aug 25; 260(18):10111-7. PubMed ID: 4019502
    [Abstract] [Full Text] [Related]

  • 25. Myopathy and phosphorylase kinase deficiency caused by a mutation in the PHKA1 gene.
    Wuyts W, Reyniers E, Ceuterick C, Storm K, de Barsy T, Martin JJ.
    Am J Med Genet A; 2005 Feb 15; 133A(1):82-4. PubMed ID: 15637709
    [Abstract] [Full Text] [Related]

  • 26. Expressed phosphorylase b kinase and its alphagammadelta subcomplex as regulatory models for the rabbit skeletal muscle holoenzyme.
    Boulatnikov IG, Peters JL, Nadeau OW, Sage JM, Daniels PJ, Kumar P, Walsh DA, Carlson GM.
    Biochemistry; 2009 Oct 27; 48(42):10183-91. PubMed ID: 19764815
    [Abstract] [Full Text] [Related]

  • 27. Liver phosphorylase kinase: characterization of two interconvertible forms and partial purification of phosphorylase kinase a.
    Doorneweerd DD, Tan AW, Nuttall FQ.
    Mol Cell Biochem; 1982 Aug 20; 47(1):45-53. PubMed ID: 7132965
    [Abstract] [Full Text] [Related]

  • 28. The effect of heart and skeletal muscle troponin complexes and calmodulin on the Ca2+-dependent reactions of phosphorylase kinase isoenzymes.
    Yoshikawa K, Usui H, Imazu M, Takeda M, Ebashi S.
    Eur J Biochem; 1983 Nov 02; 136(2):413-9. PubMed ID: 6628392
    [Abstract] [Full Text] [Related]

  • 29. Phosphorylase kinase isozymes in normal and electrically stimulated skeletal muscles.
    Lawrence JC, Krsek JA, Salsgiver WJ, Hiken JF, Salmons S, Smith RL.
    Am J Physiol; 1986 Jan 02; 250(1 Pt 1):C84-9. PubMed ID: 3942208
    [Abstract] [Full Text] [Related]

  • 30. Phosphorylase-kinase-deficient liver glycogenosis with an unusual biochemical phenotype in blood cells associated with a missense mutation in the beta subunit gene (PHKB).
    Burwinkel B, Moses SW, Kilimann MW.
    Hum Genet; 1997 Dec 02; 101(2):170-4. PubMed ID: 9402963
    [Abstract] [Full Text] [Related]

  • 31. Human muscle glycogenosis due to phosphorylase kinase deficiency associated with a nonsense mutation in the muscle isoform of the alpha subunit.
    Wehner M, Clemens PR, Engel AG, Kilimann MW.
    Hum Mol Genet; 1994 Nov 02; 3(11):1983-7. PubMed ID: 7874115
    [Abstract] [Full Text] [Related]

  • 32. Mutations in the testis/liver isoform of the phosphorylase kinase gamma subunit (PHKG2) cause autosomal liver glycogenosis in the gsd rat and in humans.
    Maichele AJ, Burwinkel B, Maire I, Søvik O, Kilimann MW.
    Nat Genet; 1996 Nov 02; 14(3):337-40. PubMed ID: 8896567
    [Abstract] [Full Text] [Related]

  • 33. Is muscle glycogenolysis impaired in X-linked phosphorylase b kinase deficiency?
    Ørngreen MC, Schelhaas HJ, Jeppesen TD, Akman HO, Wevers RA, Andersen ST, ter Laak HJ, van Diggelen OP, DiMauro S, Vissing J.
    Neurology; 2008 May 13; 70(20):1876-82. PubMed ID: 18401027
    [Abstract] [Full Text] [Related]

  • 34. X-linked liver phosphorylase kinase deficiency is associated with mutations in the human liver phosphorylase kinase alpha subunit.
    van den Berg IE, van Beurden EA, Malingré HE, van Amstel HK, Poll-The BT, Smeitink JA, Lamers WH, Berger R.
    Am J Hum Genet; 1995 Feb 13; 56(2):381-7. PubMed ID: 7847371
    [Abstract] [Full Text] [Related]

  • 35. A B2 repeat insertion generates alternate structures of the mouse muscle gamma-phosphorylase kinase gene.
    Maichele AJ, Farwell NJ, Chamberlain JS.
    Genomics; 1993 Apr 13; 16(1):139-49. PubMed ID: 8486349
    [Abstract] [Full Text] [Related]

  • 36. Caspase-3 dependent cleavage and activation of skeletal muscle phosphorylase b kinase.
    Hilder TL, Carlson GM, Haystead TA, Krebs EG, Graves LM.
    Mol Cell Biochem; 2005 Jul 13; 275(1-2):233-42. PubMed ID: 16335803
    [Abstract] [Full Text] [Related]

  • 37. Dephosphorylation and inactivation of phosphorylase kinase: subunit specificity of rabbit skeletal muscle protein phosphatases.
    Ganapathi MK, Lee EY.
    Arch Biochem Biophys; 1984 Aug 15; 233(1):19-31. PubMed ID: 6087741
    [Abstract] [Full Text] [Related]

  • 38. Quantitative genetics of age-related retinal degeneration: a second F1 intercross between the A/J and C57BL/6 strains.
    Danciger M, Yang H, Ralston R, Liu Y, Matthes MT, Peirce J, Lavail MM.
    Mol Vis; 2007 Jan 25; 13():79-85. PubMed ID: 17277741
    [Abstract] [Full Text] [Related]

  • 39. Muscle phosphorylase b kinase deficiency revisited.
    Echaniz-Laguna A, Akman HO, Mohr M, Tranchant C, Talmant-Verbist V, Rolland MO, Dimauro S.
    Neuromuscul Disord; 2010 Feb 25; 20(2):125-7. PubMed ID: 20080404
    [Abstract] [Full Text] [Related]

  • 40. Assignment of human genes for phosphorylase kinase subunits alpha (PHKA) to Xq12-q13 and beta (PHKB) to 16q12-q13.
    Francke U, Darras BT, Zander NF, Kilimann MW.
    Am J Hum Genet; 1989 Aug 25; 45(2):276-82. PubMed ID: 2757032
    [Abstract] [Full Text] [Related]

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