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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

223 related items for PubMed ID: 8733123

  • 21.
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  • 22. FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates.
    Grewal PK, Todd LC, van der Maarel S, Frants RR, Hewitt JE.
    Gene; 1998 Aug 17; 216(1):13-9. PubMed ID: 9714712
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  • 26. 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 17; 149(1):73-9. PubMed ID: 9168169
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  • 28. 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 Jul 17; (2):S6-13. PubMed ID: 23573580
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  • 29. 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 17; 74(3):322-31. PubMed ID: 11708861
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  • 31. A functional role for 4qA/B in the structural rearrangement of the 4q35 region and in the regulation of FRG1 and ANT1 in facioscapulohumeral dystrophy.
    Pirozhkova I, Petrov A, Dmitriev P, Laoudj D, Lipinski M, Vassetzky Y.
    PLoS One; 2008 Nov 17; 3(10):e3389. PubMed ID: 18852887
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  • 33. [Facioscapulohumeral muscular dystrophy (FSHD)].
    Funakoshi M, Goto K, Kim BY, Arahata K.
    Nihon Rinsho; 1997 Dec 17; 55(12):3181-5. PubMed ID: 9436432
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  • 35. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
    Gabellini D, D'Antona G, Moggio M, Prelle A, Zecca C, Adami R, Angeletti B, Ciscato P, Pellegrino MA, Bottinelli R, Green MR, Tupler R.
    Nature; 2006 Feb 23; 439(7079):973-7. PubMed ID: 16341202
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  • 40. 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 23; 5(10):1567-75. PubMed ID: 8894690
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