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Journal Abstract Search

297 related items for PubMed ID: 8069466

  • 1. The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: implications for a role of chromatin structure in the pathogenesis of the disease.
    Winokur ST, Bengtsson U, Feddersen J, Mathews KD, Weiffenbach B, Bailey H, Markovich RP, Murray JC, Wasmuth JJ, Altherr MR.
    Chromosome Res; 1994 May; 2(3):225-34. PubMed ID: 8069466
    [Abstract] [Full Text] [Related]

  • 2. High resolution fluorescence in situ hybridization to linearly extended DNA visually maps a tandem repeat associated with facioscapulohumeral muscular dystrophy immediately adjacent to the telomere of 4q.
    Bengtsson U, Altherr MR, Wasmuth JJ, Winokur ST.
    Hum Mol Genet; 1994 Oct; 3(10):1801-5. PubMed ID: 7849703
    [Abstract] [Full Text] [Related]

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

  • 4. Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy.
    Tupler R, Berardinelli A, Barbierato L, Frants R, Hewitt JE, Lanzi G, Maraschio P, Tiepolo L.
    J Med Genet; 1996 May; 33(5):366-70. PubMed ID: 8733044
    [Abstract] [Full Text] [Related]

  • 5. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.
    Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, Gruter AM, Hofker MH, Moerer P, Williamson R.
    Nat Genet; 1992 Sep; 2(1):26-30. PubMed ID: 1363881
    [Abstract] [Full Text] [Related]

  • 6. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit.
    van Deutekom JC, Wijmenga C, van Tienhoven EA, Gruter AM, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR.
    Hum Mol Genet; 1993 Dec; 2(12):2037-42. PubMed ID: 8111371
    [Abstract] [Full Text] [Related]

  • 7. Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter.
    Deidda G, Cacurri S, Grisanti P, Vigneti E, Piazzo N, Felicetti L.
    Eur J Hum Genet; 1995 Dec; 3(3):155-67. PubMed ID: 7583041
    [Abstract] [Full Text] [Related]

  • 8. Inter- and intrachromosomal sub-telomeric rearrangements on 4q35: implications for facioscapulohumeral muscular dystrophy (FSHD) aetiology and diagnosis.
    Lemmers RJ, van der Maarel SM, van Deutekom JC, van der Wielen MJ, Deidda G, Dauwerse HG, Hewitt J, Hofker M, Bakker E, Padberg GW, Frants RR.
    Hum Mol Genet; 1998 Aug; 7(8):1207-14. PubMed ID: 9668160
    [Abstract] [Full Text] [Related]

  • 9. The evolutionary distribution and structural organization of the homeobox-containing repeat D4Z4 indicates a functional role for the ancestral copy in the FSHD region.
    Winokur ST, Bengtsson U, Vargas JC, Wasmuth JJ, Altherr MR, Weiffenbach B, Jacobsen SJ.
    Hum Mol Genet; 1996 Oct; 5(10):1567-75. PubMed ID: 8894690
    [Abstract] [Full Text] [Related]

  • 10. Molecular genetics of facioscapulohumeral muscular dystrophy.
    Wijmenga C, Frants RR, Hewitt JE, van Deutekom JC, van Geel M, Wright TJ, Padberg GW, Hofker MH, van Ommen GJ.
    Neuromuscul Disord; 1993 Oct; 3(5-6):487-91. PubMed ID: 8186699
    [Abstract] [Full Text] [Related]

  • 11. Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan.
    Hsu YD, Kao MC, Shyu WC, Lin JC, Huang NE, Sun HF, Yang KD, Tsao WL.
    J Neurol Sci; 1997 Jul; 149(1):73-9. PubMed ID: 9168169
    [Abstract] [Full Text] [Related]

  • 12. Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35.
    Lee JH, Goto K, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 Jul; 2():S6-13. PubMed ID: 7739628
    [Abstract] [Full Text] [Related]

  • 13. Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35.
    van Deutekom JC, Hofker MH, Romberg S, van Geel M, Rommens J, Wright TJ, Hewitt JE, Padberg GW, Wijmenga C, Frants RR.
    Muscle Nerve Suppl; 1995 Jul; (2):S19-26. PubMed ID: 23573582
    [Abstract] [Full Text] [Related]

  • 14. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.
    Hewitt JE, Lyle R, Clark LN, Valleley EM, Wright TJ, Wijmenga C, van Deutekom JC, Francis F, Sharpe PT, Hofker M.
    Hum Mol Genet; 1994 Aug; 3(8):1287-95. PubMed ID: 7987304
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure.
    Rossi M, Ricci E, Colantoni L, Galluzzi G, Frusciante R, Tonali PA, Felicetti L.
    BMC Med Genet; 2007 Mar 02; 8():8. PubMed ID: 17335567
    [Abstract] [Full Text] [Related]

  • 17. Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.
    van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, Dauwerse HG, Wright TJ, Padberg GW, Hofker MH, Hewitt JE, Frants RR.
    Hum Mol Genet; 1996 May 02; 5(5):581-90. PubMed ID: 8733123
    [Abstract] [Full Text] [Related]

  • 18. Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).
    Lee JH, Goto K, Sahashi KO, Nonaka I, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 May 02; (2):S27-31. PubMed ID: 23573583
    [Abstract] [Full Text] [Related]

  • 19. Characterization of a tandemly repeated 3.3-kb Kpnl unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35.
    Lee JH, Goto K, Matsuda C, Arahata K.
    Muscle Nerve Suppl; 1995 May 02; (2):S6-13. PubMed ID: 23573580
    [Abstract] [Full Text] [Related]

  • 20. Evidence for subtelomeric exchange of 3.3 kb tandemly repeated units between chromosomes 4q35 and 10q26: implications for genetic counselling and etiology of FSHD1.
    van Deutekom JC, Bakker E, Lemmers RJ, van der Wielen MJ, Bik E, Hofker MH, Padberg GW, Frants RR.
    Hum Mol Genet; 1996 Dec 02; 5(12):1997-2003. PubMed ID: 8968754
    [Abstract] [Full Text] [Related]

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