Results 201 to 210 of about 37,729 (256)

Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (gutted) adenovirus-encoding murine dystrophin [PDF]

, 2003
Rénald Gilbert, Roy Dudley, An‐Bang Liu, Basil J. Petrof, Joséphine Nalbantoglu, George Karpati   +5 more
openalex   +1 more source

Implications for Cardiac Function Following Rescue of the Dystrophic Diaphragm in a Mouse Model of Duchenne Muscular Dystrophy [PDF]

A Asai, A Crisp, A De Troyer, A Malerba, A Malerba, A Malerba, BJ Petrof, C Betts, C Kirchmann, CF Spurney, DJ Stuckey, DM Connuck, G Dickson, G Nigro, H Yin, H Yin, J Alter, J Kuroda, J Morrison, JG Quinlan, JM Costas, JO Benditt, JW Carnwath, K Ito, K Ohlendieck, L Loufrani, L Loufrani, L Loufrani, M Ishizaki, M Ishizaki, M Mosqueira, M Palladino, MG Dunckley, N Jearawiriyapaisarn, P Melacini, QL Lu, S Fletcher, SD Wilton   +37 more
core   +1 more source

Maltodextrin-modified lipoplexes for enhanced mucosal penetration and efficient mRNA delivery. [PDF]

Mater Today Bio
Kopilovic B, Laroui N, Berchel M, Jaffrès PA, Midoux P, Freire MG, Pichon C.   +6 more
europepmc   +1 more source

Expression of dystrophin driven by the 1.35-kb MCK promoter ameliorates muscular dystrophy in fast, but not in slow muscles of transgenic mdx mice [PDF]

, 2003
Patrick Dunant, Nancy Larochelle, Christian Thirion, Rolf Stucka, Daniel Ursu, Basil J. Petrof, Eckhard Wolf, Hanns Lochmüller   +7 more
openalex   +1 more source

Functional cardiac consequences of β-adrenergic stress-induced injury in a model of Duchenne muscular dystrophy

Disease Models & Mechanisms
Conner C. Earl, Areli J. Javier, Alyssa M. Richards, Larry W. Markham, Craig J. Goergen, Steven S. Welc   +5 more
doaj   +1 more source

Faculty Opinions recommendation of Involvement of TRPC in the abnormal calcium influx observed in dystrophic (mdx) mouse skeletal muscle fibers.

, 2002
Roger Hardie
openalex   +2 more sources

Obligatory and accessory respiratory muscle structure, function and control in early and advanced disease in the mdx mouse model of Duchenne muscular dystrophy. [PDF]

J Physiol
Slyne AD, Burns DP, Wöller K, May A, Dowd R, Drummond SE, Jasionek G, O'Halloran KD.   +7 more
europepmc   +1 more source

Inhibition of mitochondrial fission protein Drp1 ameliorates skeletal myopathy in the D2-mdx model of Duchenne muscular dystrophy. [PDF]

Am J Physiol Cell Physiol
Rosen HG, Berger NJ, Hodge SN, Fujishiro A, Lourie J, Kapadia V, Duzz T, Linden MA, Jee E, Kim J, Kim Y, Zou K.   +11 more
europepmc   +1 more source

Enhanced therapeutic potential of a microdystrophin with an extended C-terminal domain. [PDF]

Mol Ther Methods Clin Dev
Foltz SJ, Qian R, Yang J, Elliott K, Heithoff BP, Jasick H, Smith JB, Karumuthil-Melethil S, Qiao C, Liu Y, Danos O.   +10 more
europepmc   +1 more source

miR-33 inhibition as a novel therapeutic approach for treating muscular dystrophy. [PDF]

EMBO Mol Med
Lopez MA, Alexander MS.
europepmc   +1 more source