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Journal Abstract Search

299 related items for PubMed ID: 17034757

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  • 4. [Hint and luck for identification of a gene for Fukuyama muscular dystrophy, fukutin].
    Toda T.
    Rinsho Shinkeigaku; 2007 Nov; 47(11):743-8. PubMed ID: 18210789
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  • 6. Fukutin expression in mouse non-muscle somatic organs: its relationship to the hypoglycosylation of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.
    Saito Y, Yamamoto T, Ohtsuka-Tsurumi E, Oka A, Mizuguchi M, Itoh M, Voit T, Kato Y, Kobayashi M, Saito K, Osawa M.
    Brain Dev; 2004 Oct; 26(7):469-79. PubMed ID: 15351084
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  • 7. Mislocalization of fukutin protein by disease-causing missense mutations can be rescued with treatments directed at folding amelioration.
    Tachikawa M, Kanagawa M, Yu CC, Kobayashi K, Toda T.
    J Biol Chem; 2012 Mar 09; 287(11):8398-406. PubMed ID: 22275357
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  • 8. Intracellular binding of fukutin and alpha-dystroglycan: relation to glycosylation of alpha-dystroglycan.
    Yamamoto T, Kawaguchi M, Sakayori N, Muramatsu F, Morikawa S, Kato Y, Shibata N, Kobayashi M.
    Neurosci Res; 2006 Dec 09; 56(4):391-9. PubMed ID: 17005282
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  • 9. Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan.
    Longman C, Brockington M, Torelli S, Jimenez-Mallebrera C, Kennedy C, Khalil N, Feng L, Saran RK, Voit T, Merlini L, Sewry CA, Brown SC, Muntoni F.
    Hum Mol Genet; 2003 Nov 01; 12(21):2853-61. PubMed ID: 12966029
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  • 12. Residual laminin-binding activity and enhanced dystroglycan glycosylation by LARGE in novel model mice to dystroglycanopathy.
    Kanagawa M, Nishimoto A, Chiyonobu T, Takeda S, Miyagoe-Suzuki Y, Wang F, Fujikake N, Taniguchi M, Lu Z, Tachikawa M, Nagai Y, Tashiro F, Miyazaki J, Tajima Y, Takeda S, Endo T, Kobayashi K, Campbell KP, Toda T.
    Hum Mol Genet; 2009 Feb 15; 18(4):621-31. PubMed ID: 19017726
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  • 13. [Dystroglycan linkage and muscular dystrophy].
    Shimizu T.
    Rinsho Shinkeigaku; 2002 Nov 15; 42(11):1091-4. PubMed ID: 12784674
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  • 14. Phenotypic spectrum of Fukutinopathy: most severe phenotype of Fukutinopathy.
    Yoshioka M.
    Brain Dev; 2009 Jun 15; 31(6):419-22. PubMed ID: 18834683
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  • 15. Co-localization of fukutin and alpha-dystroglycan in the mouse central nervous system.
    Ohtsuka-Tsurumi E, Saito Y, Yamamoto T, Voit T, Kobayashi M, Osawa M.
    Brain Res Dev Brain Res; 2004 Sep 17; 152(2):121-7. PubMed ID: 15351499
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  • 16. Deficiency of alpha-dystroglycan in muscle-eye-brain disease.
    Kano H, Kobayashi K, Herrmann R, Tachikawa M, Manya H, Nishino I, Nonaka I, Straub V, Talim B, Voit T, Topaloglu H, Endo T, Yoshikawa H, Toda T.
    Biochem Biophys Res Commun; 2002 Mar 15; 291(5):1283-6. PubMed ID: 11883957
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  • 17. Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.
    Matsumoto H, Hayashi YK, Kim DS, Ogawa M, Murakami T, Noguchi S, Nonaka I, Nakazawa T, Matsuo T, Futagami S, Campbell KP, Nishino I.
    Neuromuscul Disord; 2005 May 15; 15(5):342-8. PubMed ID: 15833426
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  • 18. Subcellular localization of fukutin and fukutin-related protein in muscle cells.
    Matsumoto H, Noguchi S, Sugie K, Ogawa M, Murayama K, Hayashi YK, Nishino I.
    J Biochem; 2004 Jun 15; 135(6):709-12. PubMed ID: 15213246
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  • 19. [Recent Advances in α-dystroglycanopathy].
    Kuga A, Kanagawa M, Toda T.
    Brain Nerve; 2011 Nov 15; 63(11):1189-95. PubMed ID: 22068471
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  • 20. Fukutin is prerequisite to ameliorate muscular dystrophic phenotype by myofiber-selective LARGE expression.
    Ohtsuka Y, Kanagawa M, Yu CC, Ito C, Chiyo T, Kobayashi K, Okada T, Takeda S, Toda T.
    Sci Rep; 2015 Feb 09; 5():8316. PubMed ID: 25661440
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