BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

378 related articles for article (PubMed ID: 24922526)

  • 61. The absence of dystrophin rather than muscle degeneration causes acetylcholine receptor cluster defects in dystrophic muscle.
    Kong J; Yang L; Li Q; Cao J; Yang J; Chen F; Wang Y; Zhang C
    Neuroreport; 2012 Jan; 23(2):82-7. PubMed ID: 22124255
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Aberrant RhoA activation in macrophages increases senescence-associated secretory phenotypes and ectopic calcification in muscular dystrophic mice.
    Mu X; Lin CY; Hambright WS; Tang Y; Ravuri S; Lu A; Matre P; Chen W; Gao X; Cui Y; Zhong L; Wang B; Huard J
    Aging (Albany NY); 2020 Dec; 12(24):24853-24871. PubMed ID: 33361519
    [TBL] [Abstract][Full Text] [Related]  

  • 63. CT-GalNAc transferase overexpression in adult mice is associated with extrasynaptic utrophin in skeletal muscle fibres.
    Durko M; Allen C; Nalbantoglu J; Karpati G
    J Muscle Res Cell Motil; 2010 Sep; 31(3):181-93. PubMed ID: 20706865
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Differential targeting of nNOS and AQP4 to dystrophin-deficient sarcolemma by membrane-directed alpha-dystrobrevin.
    Adams ME; Tesch Y; Percival JM; Albrecht DE; Conhaim JI; Anderson K; Froehner SC
    J Cell Sci; 2008 Jan; 121(Pt 1):48-54. PubMed ID: 18057022
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Stabilization of the cardiac sarcolemma by sarcospan rescues DMD-associated cardiomyopathy.
    Parvatiyar MS; Brownstein AJ; Kanashiro-Takeuchi RM; Collado JR; Dieseldorff Jones KM; Gopal J; Hammond KG; Marshall JL; Ferrel A; Beedle AM; Chamberlain JS; Renato Pinto J; Crosbie RH
    JCI Insight; 2019 Apr; 5(11):. PubMed ID: 31039133
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Characterization of neuromuscular synapse function abnormalities in multiple Duchenne muscular dystrophy mouse models.
    van der Pijl EM; van Putten M; Niks EH; Verschuuren JJ; Aartsma-Rus A; Plomp JJ
    Eur J Neurosci; 2016 Jun; 43(12):1623-35. PubMed ID: 27037492
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Low dystrophin levels increase survival and improve muscle pathology and function in dystrophin/utrophin double-knockout mice.
    van Putten M; Hulsker M; Young C; Nadarajah VD; Heemskerk H; van der Weerd L; 't Hoen PA; van Ommen GJ; Aartsma-Rus AM
    FASEB J; 2013 Jun; 27(6):2484-95. PubMed ID: 23460734
    [TBL] [Abstract][Full Text] [Related]  

  • 68. RhoA mediates defective stem cell function and heterotopic ossification in dystrophic muscle of mice.
    Mu X; Usas A; Tang Y; Lu A; Wang B; Weiss K; Huard J
    FASEB J; 2013 Sep; 27(9):3619-31. PubMed ID: 23704088
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Utrophin Compensates dystrophin Loss during Mouse Spermatogenesis.
    Chen HC; Chin YF; Lundy DJ; Liang CT; Chi YH; Kuo P; Hsieh PCH
    Sci Rep; 2017 Aug; 7(1):7372. PubMed ID: 28785010
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Extensive but coordinated reorganization of the membrane skeleton in myofibers of dystrophic (mdx) mice.
    Williams MW; Bloch RJ
    J Cell Biol; 1999 Mar; 144(6):1259-70. PubMed ID: 10087268
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Comparison of skeletal muscle pathology and motor function of dystrophin and utrophin deficient mouse strains.
    van Putten M; Kumar D; Hulsker M; Hoogaars WM; Plomp JJ; van Opstal A; van Iterson M; Admiraal P; van Ommen GJ; 't Hoen PA; Aartsma-Rus A
    Neuromuscul Disord; 2012 May; 22(5):406-17. PubMed ID: 22284942
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Consequences of the combined deficiency in dystrophin and utrophin on the mechanical properties and myosin composition of some limb and respiratory muscles of the mouse.
    Deconinck N; Rafael JA; Beckers-Bleukx G; Kahn D; Deconinck AE; Davies KE; Gillis JM
    Neuromuscul Disord; 1998 Aug; 8(6):362-70. PubMed ID: 9713852
    [TBL] [Abstract][Full Text] [Related]  

  • 73. Nitric oxide signalling pathway in Duchenne muscular dystrophy mice: up-regulation of L-arginine transporters.
    Ramachandran J; Schneider JS; Crassous PA; Zheng R; Gonzalez JP; Xie LH; Beuve A; Fraidenraich D; Peluffo RD
    Biochem J; 2013 Jan; 449(1):133-42. PubMed ID: 23009292
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Expression and localization of protein inhibitor of neuronal nitric oxide synthase in Duchenne muscular dystrophy.
    Guo Y; Petrof BJ; Hussain SN
    Muscle Nerve; 2001 Nov; 24(11):1468-75. PubMed ID: 11745948
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy.
    Guo C; Willem M; Werner A; Raivich G; Emerson M; Neyses L; Mayer U
    Hum Mol Genet; 2006 Mar; 15(6):989-98. PubMed ID: 16476707
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Utrophin A is essential in mediating the functional adaptations of mdx mouse muscle following chronic AMPK activation.
    Al-Rewashdy H; Ljubicic V; Lin W; Renaud JM; Jasmin BJ
    Hum Mol Genet; 2015 Mar; 24(5):1243-55. PubMed ID: 25324540
    [TBL] [Abstract][Full Text] [Related]  

  • 77. The role of Notch signaling in muscle progenitor cell depletion and the rapid onset of histopathology in muscular dystrophy.
    Mu X; Tang Y; Lu A; Takayama K; Usas A; Wang B; Weiss K; Huard J
    Hum Mol Genet; 2015 May; 24(10):2923-37. PubMed ID: 25678553
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Exercise increases utrophin protein expression in the mdx mouse model of Duchenne muscular dystrophy.
    Gordon BS; Lowe DA; Kostek MC
    Muscle Nerve; 2014 Jun; 49(6):915-8. PubMed ID: 24375286
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Systemic investigation of bone and muscle abnormalities in dystrophin/utrophin double knockout mice during postnatal development and the mechanisms.
    Gao X; Tang Y; Amra S; Sun X; Cui Y; Cheng H; Wang B; Huard J
    Hum Mol Genet; 2019 May; 28(10):1738-1751. PubMed ID: 30689868
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Overexpression of the cytotoxic T cell GalNAc transferase in skeletal muscle inhibits muscular dystrophy in mdx mice.
    Nguyen HH; Jayasinha V; Xia B; Hoyte K; Martin PT
    Proc Natl Acad Sci U S A; 2002 Apr; 99(8):5616-21. PubMed ID: 11960016
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.