BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

328 related articles for article (PubMed ID: 31306642)

  • 41. Facioscapulohumeral muscular dystrophy.
    Tawil R
    Handb Clin Neurol; 2018; 148():541-548. PubMed ID: 29478599
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Systemic antisense therapeutics inhibiting DUX4 expression ameliorates FSHD-like pathology in an FSHD mouse model.
    Lu-Nguyen N; Malerba A; Herath S; Dickson G; Popplewell L
    Hum Mol Genet; 2021 Jul; 30(15):1398-1412. PubMed ID: 33987655
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Cellular and animal models for facioscapulohumeral muscular dystrophy.
    DeSimone AM; Cohen J; Lek M; Lek A
    Dis Model Mech; 2020 Oct; 13(10):. PubMed ID: 33174531
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Neuromuscular electrical stimulation promotes development in mice of mature human muscle from immortalized human myoblasts.
    Sakellariou P; O'Neill A; Mueller AL; Stadler G; Wright WE; Roche JA; Bloch RJ
    Skelet Muscle; 2016; 6():4. PubMed ID: 26925213
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Knocking Down DUX4 in Immortalized Facioscapulohumeral Muscular Dystrophy Patient-Derived Muscle Cells.
    Lim KRQ; Yokota T
    Methods Mol Biol; 2023; 2587():197-208. PubMed ID: 36401032
    [TBL] [Abstract][Full Text] [Related]  

  • 46. β-Catenin is central to DUX4-driven network rewiring in facioscapulohumeral muscular dystrophy.
    Banerji CR; Knopp P; Moyle LA; Severini S; Orrell RW; Teschendorff AE; Zammit PS
    J R Soc Interface; 2015 Jan; 12(102):20140797. PubMed ID: 25551153
    [TBL] [Abstract][Full Text] [Related]  

  • 47. It's not all about muscle: fibroadipogenic progenitors contribute to facioscapulohumeral muscular dystrophy.
    Serra C; Wagner KR
    J Clin Invest; 2020 May; 130(5):2186-2188. PubMed ID: 32250345
    [TBL] [Abstract][Full Text] [Related]  

  • 48. WDR5 is required for DUX4 expression and its pathological effects in FSHD muscular dystrophy.
    Mocciaro E; Giambruno R; Micheloni S; Cernilogar FM; Andolfo A; Consonni C; Pannese M; Ferri G; Runfola V; Schotta G; Gabellini D
    Nucleic Acids Res; 2023 Jun; 51(10):5144-5161. PubMed ID: 37021550
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Facioscapulohumeral muscular dystrophy: genetics, gene activation and downstream signalling with regard to recent therapeutic approaches: an update.
    Schätzl T; Kaiser L; Deigner HP
    Orphanet J Rare Dis; 2021 Mar; 16(1):129. PubMed ID: 33712050
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Transcriptional and cytopathological hallmarks of FSHD in chronic DUX4-expressing mice.
    Bosnakovski D; Shams AS; Yuan C; da Silva MT; Ener ET; Baumann CW; Lindsay AJ; Verma M; Asakura A; Lowe DA; Kyba M
    J Clin Invest; 2020 May; 130(5):2465-2477. PubMed ID: 32250341
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Improving Molecular and Histopathology in Diaphragm Muscle of the Double Transgenic ACTA1-MCM/FLExDUX4 Mouse Model of FSHD with Systemic Antisense Therapy.
    Lu-Nguyen N; Malerba A; Antoni Pineda M; Dickson G; Popplewell L
    Hum Gene Ther; 2022 Sep; 33(17-18):923-935. PubMed ID: 35078334
    [TBL] [Abstract][Full Text] [Related]  

  • 52. MATR3 is an endogenous inhibitor of DUX4 in FSHD muscular dystrophy.
    Runfola V; Giambruno R; Caronni C; Pannese M; Andolfo A; Gabellini D
    Cell Rep; 2023 Sep; 42(9):113120. PubMed ID: 37703175
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Testing the effects of FSHD candidate gene expression in vertebrate muscle development.
    Wuebbles RD; Long SW; Hanel ML; Jones PL
    Int J Clin Exp Pathol; 2010 Mar; 3(4):386-400. PubMed ID: 20490329
    [TBL] [Abstract][Full Text] [Related]  

  • 54. The Genetics and Epigenetics of Facioscapulohumeral Muscular Dystrophy.
    Himeda CL; Jones PL
    Annu Rev Genomics Hum Genet; 2019 Aug; 20():265-291. PubMed ID: 31018108
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4.
    Homma S; Beermann ML; Yu B; Boyce FM; Miller JB
    Skelet Muscle; 2016 Dec; 6(1):42. PubMed ID: 27906075
    [TBL] [Abstract][Full Text] [Related]  

  • 56. A feedback loop between nonsense-mediated decay and the retrogene DUX4 in facioscapulohumeral muscular dystrophy.
    Feng Q; Snider L; Jagannathan S; Tawil R; van der Maarel SM; Tapscott SJ; Bradley RK
    Elife; 2015 Jan; 4():. PubMed ID: 25564732
    [TBL] [Abstract][Full Text] [Related]  

  • 57. A Targeted Approach for Evaluating DUX4-Regulated Proteins as Potential Serum Biomarkers for Facioscapulohumeral Muscular Dystrophy Using Immunoassay Proteomics.
    Campbell AE; Arjomand J; King OD; Tawil R; Jagannathan S
    J Neuromuscul Dis; 2023; 10(6):1031-1040. PubMed ID: 37899061
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Facioscapulohumeral dystrophy: activating an early embryonic transcriptional program in human skeletal muscle.
    Campbell AE; Belleville AE; Resnick R; Shadle SC; Tapscott SJ
    Hum Mol Genet; 2018 Aug; 27(R2):R153-R162. PubMed ID: 29718206
    [TBL] [Abstract][Full Text] [Related]  

  • 59. A cre-inducible DUX4 transgenic mouse model for investigating facioscapulohumeral muscular dystrophy.
    Jones T; Jones PL
    PLoS One; 2018; 13(2):e0192657. PubMed ID: 29415061
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Model systems of DUX4 expression recapitulate the transcriptional profile of FSHD cells.
    Jagannathan S; Shadle SC; Resnick R; Snider L; Tawil RN; van der Maarel SM; Bradley RK; Tapscott SJ
    Hum Mol Genet; 2016 Oct; 25(20):4419-4431. PubMed ID: 28171552
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.