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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

388 related items for PubMed ID: 16267784

  • 21.
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  • 22. Differential association of syntrophin pairs with the dystrophin complex.
    Peters MF, Adams ME, Froehner SC.
    J Cell Biol; 1997 Jul 14; 138(1):81-93. PubMed ID: 9214383
    [Abstract] [Full Text] [Related]

  • 23. Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface.
    Bonilla E, Samitt CE, Miranda AF, Hays AP, Salviati G, DiMauro S, Kunkel LM, Hoffman EP, Rowland LP.
    Cell; 1988 Aug 12; 54(4):447-52. PubMed ID: 3042151
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  • 24.
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  • 25. [Association between dystrophin and neuronal nitric oxide synthase in muscles of progressive muscular dystrophy].
    Wang S, Shen D.
    Zhonghua Yi Xue Za Zhi; 2002 Feb 10; 82(3):155-7. PubMed ID: 11953148
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  • 30. Deficiency of syntrophin, dystroglycan, and merosin in a female infant with a congenital muscular dystrophy phenotype lacking cysteine-rich and C-terminal domains of dystrophin.
    Tachi N, Ohya K, Chiba S, Matsuo M, Patria SY, Matsumura K.
    Neurology; 1997 Aug 10; 49(2):579-83. PubMed ID: 9270600
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  • 31. Vascular alterations in Fukuyama type congenital muscular dystrophy.
    Sugino S, Miyatake M, Ohtani Y, Yoshioka K, Miike T, Uchino M.
    Brain Dev; 1991 Aug 10; 13(2):77-81. PubMed ID: 1892223
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  • 32. Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.
    Hayashi YK, Ogawa M, Tagawa K, Noguchi S, Ishihara T, Nonaka I, Arahata K.
    Neurology; 2001 Jul 10; 57(1):115-21. PubMed ID: 11445638
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  • 33. [Dystrophin detection by immunofluorescent technique for diagnosing muscular dystrophy].
    Wang X, Xie Y, Zhang C, Liu Z.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Jun 10; 19(3):239-42. PubMed ID: 12048687
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  • 34.
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  • 35. Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy.
    Bonilla E, Schmidt B, Samitt CE, Miranda AF, Hays AP, de Oliveira AB, Chang HW, Servidei S, Ricci E, Younger DS.
    Am J Pathol; 1988 Dec 10; 133(3):440-5. PubMed ID: 3059802
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  • 37. [Expression of connective tissue growth factor in progressive muscular dystrophy].
    Sun GL, Yao F, Jiang HK, Li P, Kazuhiro H.
    Zhonghua Er Ke Za Zhi; 2005 Oct 10; 43(10):753-7. PubMed ID: 16255854
    [Abstract] [Full Text] [Related]

  • 38. Degradation of connectin (titin) in Fukuyama type congenital muscular dystrophy: immunochemical study with monoclonal antibodies.
    Matsumura K, Shimizu T, Sunada Y, Mannen T, Nonaka I, Kimura S, Maruyama K.
    J Neurol Sci; 1990 Sep 10; 98(2-3):155-62. PubMed ID: 2243226
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