Results 181 to 190 of about 1,104,554 (244)

Using muscle homing peptide CyPep10 to deliver phosphorodiamidate morpholino oligomers in the mdx mouse. [PDF]

Mol Ther Nucleic Acids
Schneider AE, Tanganyika-de Winter CL, Jirka SMG, Tan X, Thompson EG, Ha K, Mitra A, Garcia S, Luimes M, Oliver RA, Guerlavais V, Aartsma-Rus A.   +11 more
europepmc   +1 more source

Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy

, 2009
Jachinta E. Rooney, Praveen B. Gurpur, Dean J. Burkin   +2 more
openalex   +1 more source

Improvement of the mdx mouse dystrophic phenotype by systemic in utero AAV8 delivery of a minidystrophin gene

, 2020
B M Koppanati, J Li, D P Reay, B Wang, M Daood, H Zheng, X Xiao, J F Watchko, P R Clemens   +8 more
openalex   +1 more source

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

Author Correction: Humanizing the mdx mouse model of DMD: the long and the short of it. [PDF]

NPJ Regen Med, 2020
Yucel N, Chang AC, Day JW, Rosenthal N, Blau HM.   +4 more
europepmc   +1 more source

A role for caveolin-3 in the pathogenesis of the mdx mouse [PDF]

, 2012
Dean P. Larner
openalex  

Antisense-induced exon skipping and synthesis of dystrophin in the mdx mouse

, 2000
Christopher J. Mann
openalex   +1 more source

Stress exposure in the mdx mouse model of Duchenne muscular dystrophy provokes a widespread metabolic response. [PDF]

FEBS J
Johnson EE, Ervasti JM.
europepmc   +1 more source

Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation.

American Journal of Physiology - Cell Physiology, 2018
R. G. Barker, V. Wyckelsma, Hongyang Xu, R. Murphy   +3 more
semanticscholar   +1 more source

Repurposed Nrf2 activator dimethyl fumarate rescues muscle inflammation and fibrosis in an aggravated mdx mouse model of Duchenne muscular dystrophy. [PDF]

Redox Biol
Kourakis S, Timpani CA, Bagaric RM, Qi B, Ali BA, Boyer R, Spiesberger G, Kandhari N, Yan X, Kuang J, Tulangekar A, de Haan JB, Deveson-Lucas D, Stupka N, Fischer D, Rybalka E.   +15 more
europepmc   +1 more source