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Journal Abstract Search

221 related items for PubMed ID: 16632607

  • 1. Chromatin loop domain organization within the 4q35 locus in facioscapulohumeral dystrophy patients versus normal human myoblasts.
    Petrov A, Pirozhkova I, Carnac G, Laoudj D, Lipinski M, Vassetzky YS.
    Proc Natl Acad Sci U S A; 2006 May 02; 103(18):6982-7. PubMed ID: 16632607
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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 16; 18(4):448-56. PubMed ID: 19888305
    [Abstract] [Full Text] [Related]

  • 4. DNaseI hypersensitivity at gene-poor, FSH dystrophy-linked 4q35.2.
    Xu X, Tsumagari K, Sowden J, Tawil R, Boyle AP, Song L, Furey TS, Crawford GE, Ehrlich M.
    Nucleic Acids Res; 2009 Dec 16; 37(22):7381-93. PubMed ID: 19820107
    [Abstract] [Full Text] [Related]

  • 5. A nuclear matrix attachment site in the 4q35 locus has an enhancer-blocking activity in vivo: implications for the facio-scapulo-humeral dystrophy.
    Petrov A, Allinne J, Pirozhkova I, Laoudj D, Lipinski M, Vassetzky YS.
    Genome Res; 2008 Jan 16; 18(1):39-45. PubMed ID: 18032730
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 12(22):2895-907. PubMed ID: 14519683
    [Abstract] [Full Text] [Related]

  • 7. A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere.
    Thomas NS, Wiseman K, Spurlock G, MacDonald M, Ustek D, Upadhyaya M.
    J Med Genet; 2007 Mar 15; 44(3):215-8. PubMed ID: 16987949
    [Abstract] [Full Text] [Related]

  • 8. Cytogenetic and immuno-FISH analysis of the 4q subtelomeric region, which is associated with facioscapulohumeral muscular dystrophy.
    Yang F, Shao C, Vedanarayanan V, Ehrlich M.
    Chromosoma; 2004 May 15; 112(7):350-9. PubMed ID: 15138770
    [Abstract] [Full Text] [Related]

  • 9. Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
    Lemmers RJ, Wohlgemuth M, van der Gaag KJ, van der Vliet PJ, van Teijlingen CM, de Knijff P, Padberg GW, Frants RR, van der Maarel SM.
    Am J Hum Genet; 2007 Nov 15; 81(5):884-94. PubMed ID: 17924332
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. Localization of 4q35.2 to the nuclear periphery: is FSHD a nuclear envelope disease?
    Masny PS, Bengtsson U, Chung SA, Martin JH, van Engelen B, van der Maarel SM, Winokur ST.
    Hum Mol Genet; 2004 Sep 01; 13(17):1857-71. PubMed ID: 15238509
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 25(12):1781-90. PubMed ID: 26359233
    [Abstract] [Full Text] [Related]

  • 13. The Krüppel-like factor 15 as a molecular link between myogenic factors and a chromosome 4q transcriptional enhancer implicated in facioscapulohumeral dystrophy.
    Dmitriev P, Petrov A, Ansseau E, Stankevicins L, Charron S, Kim E, Bos TJ, Robert T, Turki A, Coppée F, Belayew A, Lazar V, Carnac G, Laoudj D, Lipinski M, Vassetzky YS.
    J Biol Chem; 2011 Dec 30; 286(52):44620-31. PubMed ID: 21937448
    [Abstract] [Full Text] [Related]

  • 14. Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD).
    Fisher J, Upadhyaya M.
    Neuromuscul Disord; 1997 Jan 30; 7(1):55-62. PubMed ID: 9132141
    [Abstract] [Full Text] [Related]

  • 15. Hybridization analysis of D4Z4 repeat arrays linked to FSHD.
    Ehrlich M, Jackson K, Tsumagari K, Camaño P, Lemmers RJ.
    Chromosoma; 2007 Apr 30; 116(2):107-16. PubMed ID: 17131163
    [Abstract] [Full Text] [Related]

  • 16. D4F104S1 deletion in facioscapulohumeral muscular dystrophy: phenotype, size, and detection.
    Lemmers RJ, Osborn M, Haaf T, Rogers M, Frants RR, Padberg GW, Cooper DN, van der Maarel SM, Upadhyaya M.
    Neurology; 2003 Jul 22; 61(2):178-83. PubMed ID: 12874395
    [Abstract] [Full Text] [Related]

  • 17. 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 27; 4():67. PubMed ID: 21951698
    [Abstract] [Full Text] [Related]

  • 18. 4q-D4Z4 chromatin architecture regulates the transcription of muscle atrophic genes in facioscapulohumeral muscular dystrophy.
    Cortesi A, Pesant M, Sinha S, Marasca F, Sala E, Gregoretti F, Antonelli L, Oliva G, Chiereghin C, Soldà G, Bodega B.
    Genome Res; 2019 Jun 27; 29(6):883-895. PubMed ID: 31097473
    [Abstract] [Full Text] [Related]

  • 19. Genetic and epigenetic characteristics of FSHD-associated 4q and 10q D4Z4 that are distinct from non-4q/10q D4Z4 homologs.
    Zeng W, Chen YY, Newkirk DA, Wu B, Balog J, Kong X, Ball AR, Zanotti S, Tawil R, Hashimoto N, Mortazavi A, van der Maarel SM, Yokomori K.
    Hum Mutat; 2014 Aug 27; 35(8):998-1010. PubMed ID: 24838473
    [Abstract] [Full Text] [Related]

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