BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

269 related articles for article (PubMed ID: 12868502)

  • 1. Facioscapulohumeral muscular dystrophy (FSHD) myoblasts demonstrate increased susceptibility to oxidative stress.
    Winokur ST; Barrett K; Martin JH; Forrester JR; Simon M; Tawil R; Chung SA; Masny PS; Figlewicz DA
    Neuromuscul Disord; 2003 May; 13(4):322-33. PubMed ID: 12868502
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Expression profiling of FSHD muscle supports a defect in specific stages of myogenic differentiation.
    Winokur ST; Chen YW; Masny PS; Martin JH; Ehmsen JT; Tapscott SJ; van der Maarel SM; Hayashi Y; Flanigan KM
    Hum Mol Genet; 2003 Nov; 12(22):2895-907. PubMed ID: 14519683
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Gene expression during normal and FSHD myogenesis.
    Tsumagari K; Chang SC; Lacey M; Baribault C; Chittur SV; Sowden J; Tawil R; Crawford GE; Ehrlich M
    BMC Med Genomics; 2011 Sep; 4():67. PubMed ID: 21951698
    [TBL] [Abstract][Full Text] [Related]  

  • 4. DUX4-induced constitutive DNA damage and oxidative stress contribute to aberrant differentiation of myoblasts from FSHD patients.
    Dmitriev P; Bou Saada Y; Dib C; Ansseau E; Barat A; Hamade A; Dessen P; Robert T; Lazar V; Louzada RAN; Dupuy C; Zakharova V; Carnac G; Lipinski M; Vassetzky YS
    Free Radic Biol Med; 2016 Oct; 99():244-258. PubMed ID: 27519269
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cancer-related genes in the transcription signature of facioscapulohumeral dystrophy myoblasts and myotubes.
    Dmitriev P; Kairov U; Robert T; Barat A; Lazar V; Carnac G; Laoudj-Chenivesse D; Vassetzky YS
    J Cell Mol Med; 2014 Feb; 18(2):208-17. PubMed ID: 24341522
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Defective regulation of microRNA target genes in myoblasts from facioscapulohumeral dystrophy patients.
    Dmitriev P; Stankevicins L; Ansseau E; Petrov A; Barat A; Dessen P; Robert T; Turki A; Lazar V; Labourer E; Belayew A; Carnac G; Laoudj-Chenivesse D; Lipinski M; Vassetzky YS
    J Biol Chem; 2013 Dec; 288(49):34989-5002. PubMed ID: 24145033
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Skeletal muscle regeneration in facioscapulohumeral muscular dystrophy is correlated with pathological severity.
    Banerji CRS; Henderson D; Tawil RN; Zammit PS
    Hum Mol Genet; 2020 Sep; 29(16):2746-2760. PubMed ID: 32744322
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Membrane Repair Deficit in Facioscapulohumeral Muscular Dystrophy.
    Bittel AJ; Sreetama SC; Bittel DC; Horn A; Novak JS; Yokota T; Zhang A; Maruyama R; Rowel Q Lim K; Jaiswal JK; Chen YW
    Int J Mol Sci; 2020 Aug; 21(15):. PubMed ID: 32759720
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ; Welle S; Venance SL; Thornton CA; Tawil R
    Neurology; 2007 Feb; 68(8):569-77. PubMed ID: 17151338
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Facioscapulohumeral dystrophy myoblasts efficiently repair moderate levels of oxidative DNA damage.
    Bou Saada Y; Dib C; Dmitriev P; Hamade A; Carnac G; Laoudj-Chenivesse D; Lipinski M; Vassetzky YS
    Histochem Cell Biol; 2016 Apr; 145(4):475-83. PubMed ID: 26860865
    [TBL] [Abstract][Full Text] [Related]  

  • 11. PAX7 target genes are globally repressed in facioscapulohumeral muscular dystrophy skeletal muscle.
    Banerji CRS; Panamarova M; Hebaishi H; White RB; Relaix F; Severini S; Zammit PS
    Nat Commun; 2017 Dec; 8(1):2152. PubMed ID: 29255294
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Expression profiling of FSHD-1 and FSHD-2 cells during myogenic differentiation evidences common and distinctive gene dysregulation patterns.
    Cheli S; François S; Bodega B; Ferrari F; Tenedini E; Roncaglia E; Ferrari S; Ginelli E; Meneveri R
    PLoS One; 2011; 6(6):e20966. PubMed ID: 21695143
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Dynamic transcriptomic analysis reveals suppression of PGC1α/ERRα drives perturbed myogenesis in facioscapulohumeral muscular dystrophy.
    Banerji CRS; Panamarova M; Pruller J; Figeac N; Hebaishi H; Fidanis E; Saxena A; Contet J; Sacconi S; Severini S; Zammit PS
    Hum Mol Genet; 2019 Apr; 28(8):1244-1259. PubMed ID: 30462217
    [TBL] [Abstract][Full Text] [Related]  

  • 14. p53-independent DUX4 pathology in cell and animal models of facioscapulohumeral muscular dystrophy.
    Bosnakovski D; Gearhart MD; Toso EA; Recht OO; Cucak A; Jain AK; Barton MC; Kyba M
    Dis Model Mech; 2017 Oct; 10(10):1211-1216. PubMed ID: 28754837
    [TBL] [Abstract][Full Text] [Related]  

  • 15. SORBS2 transcription is activated by telomere position effect-over long distance upon telomere shortening in muscle cells from patients with facioscapulohumeral dystrophy.
    Robin JD; Ludlow AT; Batten K; Gaillard MC; Stadler G; Magdinier F; Wright WE; Shay JW
    Genome Res; 2015 Dec; 25(12):1781-90. PubMed ID: 26359233
    [TBL] [Abstract][Full Text] [Related]  

  • 16. FSHD myotubes with different phenotypes exhibit distinct proteomes.
    Tassin A; Leroy B; Laoudj-Chenivesse D; Wauters A; Vanderplanck C; Le Bihan MC; Coppée F; Wattiez R; Belayew A
    PLoS One; 2012; 7(12):e51865. PubMed ID: 23272181
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Overexpression of the double homeodomain protein DUX4c interferes with myofibrillogenesis and induces clustering of myonuclei.
    Vanderplanck C; Tassin A; Ansseau E; Charron S; Wauters A; Lancelot C; Vancutsem K; Laoudj-Chenivesse D; Belayew A; Coppée F
    Skelet Muscle; 2018 Jan; 8(1):2. PubMed ID: 29329560
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Profiling Serum Antibodies Against Muscle Antigens in Facioscapulohumeral Muscular Dystrophy Finds No Disease-Specific Autoantibodies.
    Greco A; Straasheijm KR; Mul K; van den Heuvel A; van der Maarel SM; Joosten LAB; van Engelen BGM; Pruijn GJM
    J Neuromuscul Dis; 2021; 8(5):801-814. PubMed ID: 34024774
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ANT1 overexpression models: Some similarities with facioscapulohumeral muscular dystrophy.
    Arbogast S; Kotzur H; Frank C; Compagnone N; Sutra T; Pillard F; Pietri S; Hmada N; Moussa DMA; Bride J; Françonnet S; Mercier J; Cristol JP; Dabauvalle MC; Laoudj-Chenivesse D
    Redox Biol; 2022 Oct; 56():102450. PubMed ID: 36030628
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Interaction between mesenchymal stem cells and myoblasts in the context of facioscapulohumeral muscular dystrophy contributes to the disease phenotype.
    Kiseleva E; Serbina O; Karpukhina A; Mouly V; Vassetzky YS
    J Cell Physiol; 2022 Aug; 237(8):3328-3337. PubMed ID: 35621301
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.