Defects in neuromuscular junction structure in dystrophic muscle are corrected by expression of a NOS transgene in dystrophin-deficient muscles, but not in muscles lacking α- and 1-syntrophins

By Shiao Terry  

Human Molecular Genetics, Vol. 13, Iss. 17, 2004-09 ,pp. : 1873-1884

Oxford University Press

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Muscle-specific BCL2 expression ameliorates muscle disease in laminin α2-deficient, but not in dystrophin-deficient, mice

By Dominov Janice A.   Kravetz Amanda J.   Ardelt Magdalena   Kostek Christine A.   Beermann Mary Lou   Miller Jeffrey B.  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1029-1040

Oxford University Press

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Dissection of temporal gene expression signatures of affected and spared muscle groups in dystrophin-deficient ( mdx ) mice

By Porter J.D.  

Human Molecular Genetics, Vol. 12, Iss. 15, 2003-08 ,pp. : 1813-1821

Oxford University Press

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Temporal gene expression profiling of dystrophin-deficient ( mdx ) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy

By Porter John D.  

Human Molecular Genetics, Vol. 13, Iss. 3, 2004-02 ,pp. : 257-269

Oxford University Press

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Simple Tandem Repeat Polymorphisms in the Neuronal Nitric Oxide Synthase Gene in Different Ethnic Populations

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Human Heredity, Vol. 49, Iss. 3, 1999-05 ,pp. : 139-141

Karger

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