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Journal Abstract Search

184 related items for PubMed ID: 11092764

  • 1. Interchromosomal repeat array interactions between chromosomes 4 and 10: a model for subtelomeric plasticity.
    van Overveld PG, Lemmers RJ, Deidda G, Sandkuijl L, Padberg GW, Frants RR, van der Maarel SM.
    Hum Mol Genet; 2000 Nov 22; 9(19):2879-84. PubMed ID: 11092764
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  • 4. Hybridization analysis of D4Z4 repeat arrays linked to FSHD.
    Ehrlich M, Jackson K, Tsumagari K, Camaño P, Lemmers RJ.
    Chromosoma; 2007 Apr 22; 116(2):107-16. PubMed ID: 17131163
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  • 5. 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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  • 8. Complete allele information in the diagnosis of facioscapulohumeral muscular dystrophy by triple DNA analysis.
    Lemmers RJL, de Kievit P, van Geel M, van der Wielen MJ, Bakker E, Padberg GW, Frants RR, van der Maarel SM.
    Ann Neurol; 2001 Dec 02; 50(6):816-9. PubMed ID: 11761483
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  • 9. Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophy.
    Lemmers RJ, Wohlgemuth M, Frants RR, Padberg GW, Morava E, van der Maarel SM.
    Am J Hum Genet; 2004 Dec 02; 75(6):1124-30. PubMed ID: 15467981
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  • 14. Somatic mosaicism in FSHD often goes undetected.
    Lemmers RJ, van der Wielen MJ, Bakker E, Padberg GW, Frants RR, van der Maarel SM.
    Ann Neurol; 2004 Jun 02; 55(6):845-50. PubMed ID: 15174019
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  • 15. Exchange of subtelomeric regions between chromosomes 4q and 10q reverts the FSHD genotype and phenotype.
    Ma Y, Schwager Karpukhina A, Dib C, Gautier C, Hermine O, Allemand E, Vassetzky YS.
    Sci Adv; 2024 May 03; 10(18):eadl1922. PubMed ID: 38691604
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  • 16. Possible phenotypic dosage effect in patients compound heterozygous for FSHD-sized 4q35 alleles.
    Wohlgemuth M, Lemmers RJ, van der Kooi EL, van der Wielen MJ, van Overveld PG, Dauwerse H, Bakker E, Frants RR, Padberg GW, van der Maarel SM.
    Neurology; 2003 Oct 14; 61(7):909-13. PubMed ID: 14557558
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  • 17. 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
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  • 19. 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 22; 41(11):826-36. PubMed ID: 15520407
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