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Regulation of the cardiac L-type Ca2+ channel by the actin-binding proteins α-actinin and dystrophin
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AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2002)
Function and genetics of dystrophin and dystrophin-related proteins in muscle
DJ Blake et al.
PHYSIOLOGICAL REVIEWS (2002)
Nitric oxide-dependent modulation of sympathetic neural control of oxygenation in exercising human skeletal muscle
B Chavoshan et al.
JOURNAL OF PHYSIOLOGY-LONDON (2002)
Cytochalasin D reduces Ca2+ currents via cofilin-activated depolymerization of F-actin in guinea-pig cardiomyocytes
U Rueckschloss et al.
JOURNAL OF PHYSIOLOGY-LONDON (2001)
Alteration in calcium handling at the subcellular level in mdx myotubes
V Robert et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Cationic channels in normal and dystrophic human myotubes
C Vandebrouck et al.
NEUROMUSCULAR DISORDERS (2001)
Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy
M Sander et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Immune responses to dystrophin: implications for gene therapy of Duchenne muscular dystrophy
A Ferrer et al.
GENE THERAPY (2000)
Deflazacort increases laminin expression and myogenic repair, and induces early persistent functional gain in mdx mouse muscular dystrophy
JE Anderson et al.
CELL TRANSPLANTATION (2000)
PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): Defective regulation in failing hearts
SO Marx et al.
CELL (2000)