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Journal Abstract Search

160 related items for PubMed ID: 8894417

  • 1. The molecular genetics of human facioscapulohumeral muscular dystrophy and the myodystrophy mouse model.
    Mathews KD, Mills KA.
    Curr Opin Neurol; 1996 Oct; 9(5):394-9. PubMed ID: 8894417
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  • 2. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
    Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC.
    Muscle Nerve Suppl; 1995 Oct; 2():S98-102. PubMed ID: 7739634
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  • 3. Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q.
    Mathews KD, Mills KA, Bailey HL, Schelper RL, Murray JC.
    Muscle Nerve Suppl; 1995 Oct; (2):S98-102. PubMed ID: 23573594
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  • 8. The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.
    Bartsch JW, Mukai H, Takahashi N, Ronsiek M, Fuchs S, Jockusch H, Ono Y.
    Genomics; 1998 Apr 01; 49(1):129-32. PubMed ID: 9570957
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  • 11. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R.
    Neurology; 2007 Feb 20; 68(8):569-77. PubMed ID: 17151338
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  • 12. Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library.
    Upadhyaya M, Osborn M, Maynard J, Altherr M, Ikeda J, Harper PS.
    Am J Med Genet; 1995 Jun 19; 60(3):244-51. PubMed ID: 7573180
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  • 13. [Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy].
    Su Q, Zhang C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Oct 19; 18(5):398-401. PubMed ID: 11592052
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  • 14. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.
    Heilig R, Lemaire C, Mandel JL, Dandolo L, Amar L, Avner P.
    Nature; 2001 Oct 19; 328(6126):168-70. PubMed ID: 3600794
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  • 15. [Genetic analysis of facioscapulohumeral muscular dystrophy (FSHD)].
    Goto K, Song MD, Lee JH, Arahata K.
    Rinsho Shinkeigaku; 1995 Dec 19; 35(12):1416-8. PubMed ID: 8752415
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  • 16. 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 Dec 19; 3(5-6):487-91. PubMed ID: 8186699
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  • 17. [Facioscapulohumeral muscular dystrophy. The spectrum of clinical manifestations and molecular genetic changes].
    Krasnianski M, Neudecker S, Eger K, Schulte-Mattler W, Zierz S.
    Nervenarzt; 2003 Feb 19; 74(2):151-8. PubMed ID: 12596016
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  • 19. [Translocation between chromosomes 4q35 and 10q26 in facioscapulohumeral muscular dystrophy].
    Su QX, Zhang C, Zeng Y, Lu XL, Liu XR, Wang ZH, Zhu YZ.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Oct 19; 25(5):581-4. PubMed ID: 14650163
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  • 20. Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.
    Araki E, Nakamura K, Nakao K, Kameya S, Kobayashi O, Nonaka I, Kobayashi T, Katsuki M.
    Biochem Biophys Res Commun; 1997 Sep 18; 238(2):492-7. PubMed ID: 9299538
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