Results 161 to 170 of about 7,799 (249)

Genetic strategies for therapy of Duchenne muscular dystrophy. [PDF]

Mol Ther Nucleic Acids
Łoboda A, Chamberlain JS, Dulak J.
europepmc   +1 more source

Differential expression of dystrophin, utrophin and dystrophin‐associated proteins in peripheral nerve [PDF]

, 1993
Kiichiro Matsumura, Hiroki Yamada, Teruo Shimizu, Kevin P. Campbell   +3 more
openalex   +1 more source

Obestatin treatment links mitochondrial homeostasis and skeletal muscle repair in Duchenne muscle dystrophy. [PDF]

Mol Biomed
Lodeiro AC, Costas-Abalde S, Cid-Díaz T, Debasa-Corral L, Leal-López S, Mamchaoui K, Mouly V, Casabiell X, Gallego R, Relova JL, Pazos Y, Santos-Zas I, Camiña JP.   +12 more
europepmc   +1 more source

MicroRNA-33 inhibition ameliorates muscular dystrophy by enhancing skeletal muscle regeneration. [PDF]

EMBO Mol Med
Sowa N, Horie T, Ide Y, Baba O, Kora K, Yoshida T, Nakamura Y, Matsumura S, Matsushita K, Imanaka M, Zou F, Kume E, Kojima H, Qian Q, Kimura K, Otsuka R, Hara N, Yamasaki T, Otani C, Tsujisaka Y, Takaya T, Nishimura C, Watanabe D, Hasegawa K, Kotera J, Oka K, Fujita R, Takemiya A, Sasaki T, Kasahara Y, Obika S, Kimura T, Ono K.   +32 more
europepmc   +1 more source

35. Systemic Administration of rAAV6-Microdystrophin Preserves Muscle Function and Extends Lifespan in the Dystrophin-/Utrophin- Mouse Model of Severe Muscular Dystrophy

, 2006
Paul Gregorevic, Michael J. Blankinship, Elina Minami, James M. Allen, Charles E. Murry, Jeffrey S. Chamberlain   +5 more
openalex   +1 more source

Utrophin Lacks the Rod Domain Actin Binding Activity of Dystrophin [PDF]

, 1999
Kurt J. Amann, Athena Guo, James M. Ervasti   +2 more
openalex   +1 more source

Human dystrophin tandem calponin homology actin-binding domain crystallized in a closed-state conformation. [PDF]

Acta Crystallogr D Struct Biol
Streeter O, Shi K, Vavra J, Aihara H, Ervasti JM, Evans R, Muretta JM.   +6 more
europepmc   +1 more source

Molecular pathways involved in the control of contractile and metabolic properties of skeletal muscle fibers as potential therapeutic targets for Duchenne muscular dystrophy. [PDF]

Front Physiol
Bonato A, Raparelli G, Caruso M.
europepmc   +1 more source

The α-Syntrophin PH and PDZ Domains Scaffold Acetylcholine Receptors, Utrophin, and Neuronal Nitric Oxide Synthase at the Neuromuscular Junction [PDF]

, 2010
Marvin E. Adams, Kendra Anderson, Stanley C. Froehner   +2 more
openalex   +1 more source

Cardiac Cell and Animal Models for Duchenne Muscular Dystrophy in the Era of Gene Therapy and Precision Medicine. [PDF]

Cells
Moriyama H, Yokota T.
europepmc   +1 more source