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Journal Abstract Search

109 related items for PubMed ID: 8894690

  • 1. 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]

  • 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
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  • 3. The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.
    Lyle R, Wright TJ, Clark LN, Hewitt JE.
    Genomics; 1995 Aug 10; 28(3):389-97. PubMed ID: 7490072
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  • 4. Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat family.
    Clark LN, Koehler U, Ward DC, Wienberg J, Hewitt JE.
    Chromosoma; 1996 Sep 10; 105(3):180-9. PubMed ID: 8781186
    [Abstract] [Full Text] [Related]

  • 5. 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 10; 2(3):225-34. PubMed ID: 8069466
    [Abstract] [Full Text] [Related]

  • 6. 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 10; 3(8):1287-95. PubMed ID: 7987304
    [Abstract] [Full Text] [Related]

  • 7. Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD).
    Fisher J, Upadhyaya M.
    Neuromuscul Disord; 1997 Jan 10; 7(1):55-62. PubMed ID: 9132141
    [Abstract] [Full Text] [Related]

  • 8. 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.
    Hum Mol Genet; 1997 Mar 10; 6(3):502. PubMed ID: 9147656
    [No Abstract] [Full Text] [Related]

  • 9. Genomic analysis of facioscapulohumeral muscular dystrophy.
    Clapp J, Bolland DJ, Hewitt JE.
    Brief Funct Genomic Proteomic; 2003 Oct 10; 2(3):213-23. PubMed ID: 15239924
    [Abstract] [Full Text] [Related]

  • 10. 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
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  • 13. 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
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  • 14. Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin.
    van Geel M, Dickson MC, Beck AF, Bolland DJ, Frants RR, van der Maarel SM, de Jong PJ, Hewitt JE.
    Genomics; 2002 Feb 02; 79(2):210-7. PubMed ID: 11829491
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  • 15. Hybridization analysis of D4Z4 repeat arrays linked to FSHD.
    Ehrlich M, Jackson K, Tsumagari K, Camaño P, Lemmers RJ.
    Chromosoma; 2007 Apr 02; 116(2):107-16. PubMed ID: 17131163
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  • 16. 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 Apr 02; (2):S6-13. PubMed ID: 23573580
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  • 18. 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 Apr 02; (2):S19-26. PubMed ID: 23573582
    [Abstract] [Full Text] [Related]

  • 19. Evolutionary conservation of a coding function for D4Z4, the tandem DNA repeat mutated in facioscapulohumeral muscular dystrophy.
    Clapp J, Mitchell LM, Bolland DJ, Fantes J, Corcoran AE, Scotting PJ, Armour JA, Hewitt JE.
    Am J Hum Genet; 2007 Aug 02; 81(2):264-79. PubMed ID: 17668377
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  • 20. Worldwide population analysis of the 4q and 10q subtelomeres identifies only four discrete interchromosomal sequence transfers in human evolution.
    Lemmers RJ, van der Vliet PJ, van der Gaag KJ, Zuniga S, Frants RR, de Knijff P, van der Maarel SM.
    Am J Hum Genet; 2010 Mar 12; 86(3):364-77. PubMed ID: 20206332
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