Defective integrin switch and matrix composition at alpha 7-deficient myotendinous junctions precede the onset of muscular dystrophy in mice

By Nawrotzki R.  

Human Molecular Genetics, Vol. 12, Iss. 5, 2003-03 ,pp. : 483-495

Oxford University Press

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Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the α M β 2 leukocyte integrin receptor

By Vidal Berta   Ardite Esther   Suelves Mònica   Ruiz-Bonilla Vanessa   Janué Anna   Flick Matthew J.   Degen Jay L.   Serrano Antonio L.   Muñoz-Cánoves Pura  

Human Molecular Genetics, Vol. 21, Iss. 9, 2012-05 ,pp. : 1989-2004

Oxford University Press

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Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for Duchenne muscular dystrophy

By Ahmad A.  

Human Molecular Genetics, Vol. 9, Iss. 17, 2000-10 ,pp. : 2507-2515

Oxford University Press

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A Cysteine 3340 Substitution in the Dystroglycan-Binding Domain of Dystrophin Associated with Duchenne Muscular Dystrophy, Mental Retardation and Absence of the ERG b-Wave

By Lenk Uwe  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 973-975

Oxford University Press

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Myogenic Akt signaling attenuates muscular degeneration, promotes myofiber regeneration and improves muscle function in dystrophin-deficient mdx mice

By Kim Michelle H.   Kay Danielle I.   Rudra Renuka T.   Chen Bo Ming   Hsu Nigel   Izumiya Yasuhiro   Martinez Leonel   Spencer Melissa J.   Walsh Kenneth   Grinnell Alan D.   Crosbie Rachelle H.  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1324-1338

Oxford University Press

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