BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 11084353)

  • 1. Muscular dystrophy: the worm turns to genetic disease.
    Chamberlain JS; Benian GM
    Curr Biol; 2000 Nov; 10(21):R795-7. PubMed ID: 11084353
    [TBL] [Abstract][Full Text] [Related]  

  • 2.
    Ellwood RA; Piasecki M; Szewczyk NJ
    Int J Mol Sci; 2021 May; 22(9):. PubMed ID: 34063069
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transcriptome changes during the initiation and progression of Duchenne muscular dystrophy in Caenorhabditis elegans.
    Hrach HC; O'Brien S; Steber HS; Newbern J; Rawls A; Mangone M
    Hum Mol Genet; 2020 Jun; 29(10):1607-1623. PubMed ID: 32227114
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic suppression of phenotypes arising from mutations in dystrophin-related genes in Caenorhabditis elegans.
    Gieseler K; Grisoni K; Ségalat L
    Curr Biol; 2000 Sep; 10(18):1092-7. PubMed ID: 10996789
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prednisone reduces muscle degeneration in dystrophin-deficient Caenorhabditis elegans.
    Gaud A; Simon JM; Witzel T; Carre-Pierrat M; Wermuth CG; Ségalat L
    Neuromuscul Disord; 2004 Jun; 14(6):365-70. PubMed ID: 15145337
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Repression of phosphatidylinositol transfer protein α ameliorates the pathology of Duchenne muscular dystrophy.
    Vieira NM; Spinazzola JM; Alexander MS; Moreira YB; Kawahara G; Gibbs DE; Mead LC; Verjovski-Almeida S; Zatz M; Kunkel LM
    Proc Natl Acad Sci U S A; 2017 Jun; 114(23):6080-6085. PubMed ID: 28533404
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Gene expression profiling studies on Caenorhabditis elegans dystrophin mutants dys-1(cx-35) and dys-1(cx18).
    Towers PR; Lescure P; Baban D; Malek JA; Duarte J; Jones E; Davies KE; Ségalat L; Sattelle DB
    Genomics; 2006 Nov; 88(5):642-9. PubMed ID: 16962739
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Shrinking genes for therapy.
    Bonetta L
    Nat Med; 2002 Mar; 8(3):222. PubMed ID: 11875490
    [No Abstract]   [Full Text] [Related]  

  • 9. Overexpression of dystrobrevin delays locomotion defects and muscle degeneration in a dystrophin-deficient Caenorhabditis elegans.
    Gieseler K; Grisoni K; Mariol MC; Ségalat L
    Neuromuscul Disord; 2002 May; 12(4):371-7. PubMed ID: 12062255
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Duchenne muscular dystrophy: stalled at the junction?
    Ségalat L; Anderson JE
    Eur J Hum Genet; 2005 Jan; 13(1):4-5. PubMed ID: 15483645
    [No Abstract]   [Full Text] [Related]  

  • 11. Ultra-structural time-course study in the C. elegans model for Duchenne muscular dystrophy highlights a crucial role for sarcomere-anchoring structures and sarcolemma integrity in the earliest steps of the muscle degeneration process.
    Brouilly N; Lecroisey C; Martin E; Pierson L; Mariol MC; Qadota H; Labouesse M; Streichenberger N; Mounier N; Gieseler K
    Hum Mol Genet; 2015 Nov; 24(22):6428-45. PubMed ID: 26358775
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Dystrophin-deficient zebrafish feature aspects of the Duchenne muscular dystrophy pathology.
    Berger J; Berger S; Hall TE; Lieschke GJ; Currie PD
    Neuromuscul Disord; 2010 Dec; 20(12):826-32. PubMed ID: 20850317
    [TBL] [Abstract][Full Text] [Related]  

  • 13. What do animal models have to tell us regarding Duchenne muscular dystrophy?
    Wells DJ; Wells KE
    Acta Myol; 2005 Dec; 24(3):172-80. PubMed ID: 16629050
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript.
    Todeschini A; Gualandi F; Trabanelli C; Armaroli A; Ravani A; Fanin M; Rota S; Bello L; Ferlini A; Pegoraro E; Padovani A; Filosto M
    Neuromuscul Disord; 2016 Oct; 26(10):662-665. PubMed ID: 27616544
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation-Based Therapy for Duchenne Muscular Dystrophy: Antisense Treatment Arrives in the Clinic.
    McNally EM; Wyatt EJ
    Circulation; 2017 Sep; 136(11):979-981. PubMed ID: 28893959
    [No Abstract]   [Full Text] [Related]  

  • 16. The worm in us - Caenorhabditis elegans as a model of human disease.
    Baumeister R; Ge L
    Trends Biotechnol; 2002 Apr; 20(4):147-8. PubMed ID: 11906745
    [No Abstract]   [Full Text] [Related]  

  • 17. IGF-II ameliorates the dystrophic phenotype and coordinately down-regulates programmed cell death.
    Smith J; Goldsmith C; Ward A; LeDieu R
    Cell Death Differ; 2000 Nov; 7(11):1109-18. PubMed ID: 11139285
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [C. elegans as a model for human inherited degenerative diseases].
    Ségalat L; Néri C
    Med Sci (Paris); 2003 Dec; 19(12):1218-25. PubMed ID: 14691746
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice.
    Burkin DJ; Wallace GQ; Nicol KJ; Kaufman DJ; Kaufman SJ
    J Cell Biol; 2001 Mar; 152(6):1207-18. PubMed ID: 11257121
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Genotype-phenotype discordance in a Duchenne muscular dystrophy patient due to a novel mutation: insights into the shock absorber function of dystrophin].
    López-Hernández LB; van Heusden D; Soriano-Ursúa MA; Figuera-Villanueva L; Vázquez-Cárdenas NA; Canto P; Gómez-Díaz B; Coral-Vázquez RM
    Rev Neurol; 2011 Jun; 52(12):720-4. PubMed ID: 21594857
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.