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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

243 related items for PubMed ID: 18490429

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  • 8. Expression of the murine Pomt1 gene in both the developing brain and adult muscle tissues and its relationship with clinical aspects of Walker-Warburg syndrome.
    Prados B, Peña A, Cotarelo RP, Valero MC, Cruces J.
    Am J Pathol; 2007 May; 170(5):1659-68. PubMed ID: 17456771
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  • 11. O-mannosylation in mammalian cells.
    Endo T, Manya H.
    Methods Mol Biol; 2006 May; 347():43-56. PubMed ID: 17072003
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  • 12. Characterization of POMT2, a novel member of the PMT protein O-mannosyltransferase family specifically localized to the acrosome of mammalian spermatids.
    Willer T, Amselgruber W, Deutzmann R, Strahl S.
    Glycobiology; 2002 Nov; 12(11):771-83. PubMed ID: 12460945
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  • 13. An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene.
    Balci B, Uyanik G, Dincer P, Gross C, Willer T, Talim B, Haliloglu G, Kale G, Hehr U, Winkler J, Topaloğlu H.
    Neuromuscul Disord; 2005 Apr; 15(4):271-5. PubMed ID: 15792865
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  • 15. Expression and localization of fukutin, POMGnT1, and POMT1 in the central nervous system: consideration for functions of fukutin.
    Yamamoto T, Kato Y, Kawaguchi M, Shibata N, Kobayashi M.
    Med Electron Microsc; 2004 Dec; 37(4):200-7. PubMed ID: 15614444
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  • 16. Different roles of the two components of human protein O-mannosyltransferase, POMT1 and POMT2.
    Akasaka-Manya K, Manya H, Hayashi M, Endo T.
    Biochem Biophys Res Commun; 2011 Aug 12; 411(4):721-5. PubMed ID: 21782786
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  • 20. Glyc-O-genetics of Walker-Warburg syndrome.
    van Reeuwijk J, Brunner HG, van Bokhoven H.
    Clin Genet; 2005 Apr 12; 67(4):281-9. PubMed ID: 15733261
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