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 *

98 related articles for article (PubMed ID: 3115318)

  • 21. Relationship of genotype and in vitro contractility in mdg/mdg in equilibrium +/+ "mosaic" myotubes.
    Peterson A; Pena S
    Muscle Nerve; 1984; 7(3):194-203. PubMed ID: 6708965
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Muscular dysgenesis in mice: a model system for studying excitation-contraction coupling.
    Adams BA; Beam KG
    FASEB J; 1990 Jul; 4(10):2809-16. PubMed ID: 2165014
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Ca2+ sparks in embryonic mouse skeletal muscle selectively deficient in dihydropyridine receptor alpha1S or beta1a subunits.
    Conklin MW; Powers P; Gregg RG; Coronado R
    Biophys J; 1999 Feb; 76(2):657-69. PubMed ID: 9929471
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Prolonged depolarization promotes fast gating kinetics of L-type Ca2+ channels in mouse skeletal myotubes.
    O'Connell KM; Dirksen RT
    J Physiol; 2000 Dec; 529 Pt 3(Pt 3):647-59. PubMed ID: 11118495
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Development of the excitation-contraction coupling machinery and its relation to myofibrillogenesis in human iPSC-derived skeletal myocytes.
    Lainé J; Skoglund G; Fournier E; Tabti N
    Skelet Muscle; 2018 Jan; 8(1):1. PubMed ID: 29304851
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Ca2+-dependent excitation-contraction coupling triggered by the heterologous cardiac/brain DHPR beta2a-subunit in skeletal myotubes.
    Sheridan DC; Carbonneau L; Ahern CA; Nataraj P; Coronado R
    Biophys J; 2003 Dec; 85(6):3739-57. PubMed ID: 14645065
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Restoration of normal function in genetically defective myotubes by spontaneous fusion with fibroblasts.
    Chaudhari N; Delay R; Beam KG
    Nature; 1989 Oct; 341(6241):445-7. PubMed ID: 2507925
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Triad formation: organization and function of the sarcoplasmic reticulum calcium release channel and triadin in normal and dysgenic muscle in vitro.
    Flucher BE; Andrews SB; Fleischer S; Marks AR; Caswell A; Powell JA
    J Cell Biol; 1993 Dec; 123(5):1161-74. PubMed ID: 8245124
    [TBL] [Abstract][Full Text] [Related]  

  • 29. S165F mutation of junctophilin 2 affects Ca2+ signalling in skeletal muscle.
    Woo JS; Hwang JH; Ko JK; Weisleder N; Kim DH; Ma J; Lee EH
    Biochem J; 2010 Mar; 427(1):125-34. PubMed ID: 20095964
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Appearance of contractile activity in muscular dysgenesis (mdg/mdg) mouse myotubes during coculture with normal spinal cord cells.
    Koenig J; Bournaud R; Powell JA; Rieger F
    Dev Biol; 1982 Jul; 92(1):188-96. PubMed ID: 7106378
    [No Abstract]   [Full Text] [Related]  

  • 31. Perchlorate potentiation of excitation-contraction coupling in mammalian skeletal muscles.
    Gallant EM; Taus NS; Fletcher TF; Lentz LR; Louis CF; Mickelson JR
    Am J Physiol; 1993 Mar; 264(3 Pt 1):C559-67. PubMed ID: 8384784
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Muscular dysgenesis in the mouse (mdg/mdg). I. Ultrastructural study of skeletal and cardiac muscle.
    Banker BQ
    J Neuropathol Exp Neurol; 1977 Jan; 36(1):100-27. PubMed ID: 137961
    [TBL] [Abstract][Full Text] [Related]  

  • 33. T-tubule depolarization-induced SR Ca2+ release is controlled by dihydropyridine receptor- and Ca(2+)-dependent mechanisms in cell homogenates from rabbit skeletal muscle.
    Anderson K; Meissner G
    J Gen Physiol; 1995 Mar; 105(3):363-83. PubMed ID: 7769380
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Effects of perchlorate on the molecules of excitation-contraction coupling of skeletal and cardiac muscle.
    Ma J; Anderson K; Shirokov R; Levis R; González A; Karhanek M; Hosey MM; Meissner G; Ríos E
    J Gen Physiol; 1993 Sep; 102(3):423-48. PubMed ID: 8245818
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Abnormal enwrapment of intramuscular axons by distal Schwann cells with defective basal lamina in the muscular dysgenic mouse embryo.
    Pinçon-Raymond M; Murawsky M; Mege RM; Rieger F
    Dev Biol; 1987 Nov; 124(1):259-68. PubMed ID: 3666308
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The pore region of the skeletal muscle ryanodine receptor is a primary locus for excitation-contraction uncoupling in central core disease.
    Avila G; O'Connell KM; Dirksen RT
    J Gen Physiol; 2003 Apr; 121(4):277-86. PubMed ID: 12642598
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling.
    Tanabe T; Beam KG; Adams BA; Niidome T; Numa S
    Nature; 1990 Aug; 346(6284):567-9. PubMed ID: 2165570
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Effects of the muscular dysgenesis gene on developmental stability in the mouse mandible.
    Atchley WR; Herring SW; Riska B; Plummer AA
    J Craniofac Genet Dev Biol; 1984; 4(3):179-89. PubMed ID: 6501560
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The effect of internal sodium and caesium on phasic contraction of patch-clamped rabbit ventricular myocytes.
    Levi AJ; Mitcheson JS; Hancox JC
    J Physiol; 1996 Apr; 492 ( Pt 1)(Pt 1):1-19. PubMed ID: 8730578
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Early effects in vitro of the muscular dysgenesis mutation on nervous tissue in the mouse.
    Wieczorek DF
    Muscle Nerve; 1984; 7(3):179-93. PubMed ID: 6708964
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.