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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

239 related items for PubMed ID: 16341202

  • 1. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
    Gabellini D, D'Antona G, Moggio M, Prelle A, Zecca C, Adami R, Angeletti B, Ciscato P, Pellegrino MA, Bottinelli R, Green MR, Tupler R.
    Nature; 2006 Feb 23; 439(7079):973-7. PubMed ID: 16341202
    [Abstract] [Full Text] [Related]

  • 2. Direct interplay between two candidate genes in FSHD muscular dystrophy.
    Ferri G, Huichalaf CH, Caccia R, Gabellini D.
    Hum Mol Genet; 2015 Mar 01; 24(5):1256-66. PubMed ID: 25326393
    [Abstract] [Full Text] [Related]

  • 3. Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation.
    Bodega B, Ramirez GD, Grasser F, Cheli S, Brunelli S, Mora M, Meneveri R, Marozzi A, Mueller S, Battaglioli E, Ginelli E.
    BMC Biol; 2009 Jul 16; 7():41. PubMed ID: 19607661
    [Abstract] [Full Text] [Related]

  • 4. FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1).
    Feeney SJ, McGrath MJ, Sriratana A, Gehrig SM, Lynch GS, D'Arcy CE, Price JT, McLean CA, Tupler R, Mitchell CA.
    PLoS One; 2015 Jul 16; 10(2):e0117665. PubMed ID: 25695429
    [Abstract] [Full Text] [Related]

  • 5. Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).
    Pistoni M, Shiue L, Cline MS, Bortolanza S, Neguembor MV, Xynos A, Ares M, Gabellini D.
    PLoS Genet; 2013 Jul 16; 9(1):e1003186. PubMed ID: 23300487
    [Abstract] [Full Text] [Related]

  • 6. AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy.
    Bortolanza S, Nonis A, Sanvito F, Maciotta S, Sitia G, Wei J, Torrente Y, Di Serio C, Chamberlain JR, Gabellini D.
    Mol Ther; 2011 Nov 16; 19(11):2055-64. PubMed ID: 21829175
    [Abstract] [Full Text] [Related]

  • 7. 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 20; 68(8):569-77. PubMed ID: 17151338
    [Abstract] [Full Text] [Related]

  • 8. Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD).
    Jones TI, Parilla M, Jones PL.
    PLoS One; 2016 Feb 20; 11(3):e0150938. PubMed ID: 26942723
    [Abstract] [Full Text] [Related]

  • 9. Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle.
    Gabellini D, Green MR, Tupler R.
    Cell; 2002 Aug 09; 110(3):339-48. PubMed ID: 12176321
    [Abstract] [Full Text] [Related]

  • 10. Molecular basis of facioscapulohumeral muscular dystrophy.
    Tupler R, Gabellini D.
    Cell Mol Life Sci; 2004 Mar 09; 61(5):557-566. PubMed ID: 15004695
    [Abstract] [Full Text] [Related]

  • 11. Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1).
    Sancisi V, Germinario E, Esposito A, Morini E, Peron S, Moggio M, Tomelleri G, Danieli-Betto D, Tupler R.
    Am J Physiol Regul Integr Comp Physiol; 2014 Jan 15; 306(2):R124-37. PubMed ID: 24305066
    [Abstract] [Full Text] [Related]

  • 12. Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.
    Masny PS, Chan OY, de Greef JC, Bengtsson U, Ehrlich M, Tawil R, Lock LF, Hewitt JE, Stocksdale J, Martin JH, van der Maarel SM, Winokur ST.
    Eur J Hum Genet; 2010 Apr 15; 18(4):448-56. PubMed ID: 19888305
    [Abstract] [Full Text] [Related]

  • 13. Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein.
    Hanel ML, Sun CY, Jones TI, Long SW, Zanotti S, Milner D, Jones PL.
    Differentiation; 2011 Feb 15; 81(2):107-18. PubMed ID: 20970242
    [Abstract] [Full Text] [Related]

  • 14. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.
    Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, Ehrlich M.
    Hum Mol Genet; 2003 Nov 15; 12(22):2909-21. PubMed ID: 14506132
    [Abstract] [Full Text] [Related]

  • 15. The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.
    Grewal PK, van Deutekom JC, Mills KA, Lemmers RJ, Mathews KD, Frants RR, Hewitt JE.
    Mamm Genome; 1997 Jun 15; 8(6):394-8. PubMed ID: 9166581
    [Abstract] [Full Text] [Related]

  • 16. FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy.
    Wuebbles RD, Hanel ML, Jones PL.
    Dis Model Mech; 2009 Jun 15; 2(5-6):267-74. PubMed ID: 19383939
    [Abstract] [Full Text] [Related]

  • 17. Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level.
    Klooster R, Straasheijm K, Shah B, Sowden J, Frants R, Thornton C, Tawil R, van der Maarel S.
    Eur J Hum Genet; 2009 Dec 15; 17(12):1615-24. PubMed ID: 19809486
    [Abstract] [Full Text] [Related]

  • 18. FRG2, an FSHD candidate gene, is transcriptionally upregulated in differentiating primary myoblast cultures of FSHD patients.
    Rijkers T, Deidda G, van Koningsbruggen S, van Geel M, Lemmers RJ, van Deutekom JC, Figlewicz D, Hewitt JE, Padberg GW, Frants RR, van der Maarel SM.
    J Med Genet; 2004 Nov 15; 41(11):826-36. PubMed ID: 15520407
    [Abstract] [Full Text] [Related]

  • 19. Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD).
    Fisher J, Upadhyaya M.
    Neuromuscul Disord; 1997 Jan 15; 7(1):55-62. PubMed ID: 9132141
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.