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Journal Abstract Search

198 related items for PubMed ID: 11829491

  • 1. 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; 79(2):210-7. PubMed ID: 11829491
    [Abstract] [Full Text] [Related]

  • 2. 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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  • 3. Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.
    Lemmers RJ, de Kievit P, Sandkuijl L, Padberg GW, van Ommen GJ, Frants RR, van der Maarel SM.
    Nat Genet; 2002 Oct 02; 32(2):235-6. PubMed ID: 12355084
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  • 4. 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
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  • 5. Genomic analysis of facioscapulohumeral muscular dystrophy.
    Clapp J, Bolland DJ, Hewitt JE.
    Brief Funct Genomic Proteomic; 2003 Oct 15; 2(3):213-23. PubMed ID: 15239924
    [Abstract] [Full Text] [Related]

  • 6. The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements.
    van Geel M, Heather LJ, Lyle R, Hewitt JE, Frants RR, de Jong PJ.
    Genomics; 1999 Oct 01; 61(1):55-65. PubMed ID: 10512680
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 41(11):826-36. PubMed ID: 15520407
    [Abstract] [Full Text] [Related]

  • 8. [Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy].
    Wang N, Wu ZY, Wang CD, Wang ZQ, Lin MT, Fang L, Murong SX.
    Zhonghua Yi Xue Za Zhi; 2003 Apr 25; 83(8):650-3. PubMed ID: 12887821
    [Abstract] [Full Text] [Related]

  • 9. Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2).
    Bodega B, Cardone MF, Müller S, Neusser M, Orzan F, Rossi E, Battaglioli E, Marozzi A, Riva P, Rocchi M, Meneveri R, Ginelli E.
    BMC Evol Biol; 2007 Mar 14; 7():39. PubMed ID: 17359533
    [Abstract] [Full Text] [Related]

  • 10. Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
    Tsien F, Sun B, Hopkins NE, Vedanarayanan V, Figlewicz D, Winokur S, Ehrlich M.
    Mol Genet Metab; 2001 Nov 14; 74(3):322-31. PubMed ID: 11708861
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  • 13. Distinguishing the 4qA and 4qB variants is essential for the diagnosis of facioscapulohumeral muscular dystrophy in the Chinese population.
    Wang ZQ, Wang N, van der Maarel S, Murong SX, Wu ZY.
    Eur J Hum Genet; 2011 Jan 14; 19(1):64-9. PubMed ID: 20736973
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  • 14. [Characteristics of gene structure in facioscapulohumeral muscular dystrophy-related 4q35 subtelomere and genotype-phenotype correlation in Chinese Han population].
    Wang ZQ, Wu ZY, Wang N, Lin MT, Murong SX.
    Zhonghua Yi Xue Za Zhi; 2009 Feb 10; 89(5):304-9. PubMed ID: 19563705
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  • 16. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
    Deak KL, Lemmers RJ, Stajich JM, Klooster R, Tawil R, Frants RR, Speer MC, van der Maarel SM, Gilbert JR.
    Neurology; 2007 Feb 20; 68(8):578-82. PubMed ID: 17229919
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  • 17. Hybridization analysis of D4Z4 repeat arrays linked to FSHD.
    Ehrlich M, Jackson K, Tsumagari K, Camaño P, Lemmers RJ.
    Chromosoma; 2007 Apr 20; 116(2):107-16. PubMed ID: 17131163
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  • 19. Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD.
    de Greef JC, Wohlgemuth M, Chan OA, Hansson KB, Smeets D, Frants RR, Weemaes CM, Padberg GW, van der Maarel SM.
    Neurology; 2007 Sep 04; 69(10):1018-26. PubMed ID: 17785671
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