Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retina

By Howard P.L.  

Human Molecular Genetics, Vol. 7, Iss. 9, 1998-09 ,pp. : 1385-1391

Oxford University Press

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Expression of the dystrophin isoform Dp71 in differentiating human fetal myogenic cultures

By Tennyson Christine N.   Dally Ghassan Y.   Ray Peter N.   Worton Ronald G.  

Human Molecular Genetics, Vol. 5, Iss. 10, 1996-10 ,pp. : 1559-1566

Oxford University Press

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Targeted inactivation of dystrophin gene product Dp71: phenotypic impact in mouse retina

By Mornet D.  

Human Molecular Genetics, Vol. 12, Iss. 13, 2003-07 ,pp. : 1543-1554

Oxford University Press

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Nell1-deficient mice have reduced expression of extracellular matrix proteins causing cranial and vertebral defects

By Desai Jayashree   Shannon Mark E.   Johnson Mahlon D.   Ruff David W.   Hughes Lori A.   Kerley Marilyn K.   Carpenter Donald A.   Johnson Dabney K.   Rinchik Eugene M.   Culiat Cymbeline T.  

Human Molecular Genetics, Vol. 15, Iss. 8, 2006-04 ,pp. : 1329-1341

Oxford University Press

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Upregulation of brain utrophin does not rescue behavioral alterations in dystrophin-deficient mice

By Perronnet Caroline   Chagneau Carine   Le Blanc Pascale   Samson-Desvignes Nathalie   Mornet Dominique   Laroche Serge   De La Porte Sabine   Vaillend Cyrille  

Human Molecular Genetics, Vol. 21, Iss. 10, 2012-05 ,pp. : 2263-2276

Oxford University Press

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