Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression
about
Disrupted membrane structure and intracellular Ca²⁺ signaling in adult skeletal muscle with acute knockdown of Bin1.The zebrafish dag1 mutant: a novel genetic model for dystroglycanopathies.Localized nuclear and perinuclear Ca(2+) signals in intact mouse skeletal muscle fibers.Hyperactive intracellular calcium signaling associated with localized mitochondrial defects in skeletal muscle of an animal model of amyotrophic lateral sclerosisMicroarchitecture is severely compromised but motor protein function is preserved in dystrophic mdx skeletal muscle.Analysis of osmotic stress induced Ca2+ spark termination in mammalian skeletal muscle.Altered Ca(2+) signaling in skeletal muscle fibers of the R6/2 mouse, a model of Huntington's diseaseLong-term blocking of calcium channels in mdx mice results in differential effects on heart and skeletal muscleThe Sick and the Weak: Neuropathies/Myopathies in the Critically Ill.Nitrosative stress elicited by nNOSµ delocalization inhibits muscle force in dystrophin-null miceAssessment of calcium sparks in intact skeletal muscle fibersUtrophin suppresses low frequency oscillations and coupled gating of mechanosensitive ion channels in dystrophic skeletal muscleElevated extracellular glucose and uncontrolled type 1 diabetes enhance NFAT5 signaling and disrupt the transverse tubular network in mouse skeletal muscleComparative proteomic profiling of soleus, extensor digitorum longus, flexor digitorum brevis and interosseus muscles from the mdx mouse model of Duchenne muscular dystrophyThe common hereditary elliptocytosis-associated α-spectrin L260P mutation perturbs erythrocyte membranes by stabilizing spectrin in the closed dimer conformation.DHPR activation underlies SR Ca2+ release induced by osmotic stress in isolated rat skeletal muscle fibersCardiac and respiratory dysfunction in Duchenne muscular dystrophy and the role of second messengers.Myofibrillar misalignment correlated to triad disappearance of mdx mouse gastrocnemius muscle probed by SHG microscopy.Drug Discovery of Therapies for Duchenne Muscular Dystrophy.New factors contributing to dynamic calcium regulation in the skeletal muscle triad-a crowded placeDetection of calcium sparks in intact and permeabilized skeletal muscle fibers.Altered functional differentiation of mesoangioblasts in a genetic myopathyPartial opening and subconductance gating of mechanosensitive ion channels in dystrophic skeletal muscle.Calcium-induced release of calcium in muscle: 50 years of work and the emerging consensus.
P2860
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P2860
Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression
description
2008 nî lūn-bûn
@nan
2008 թուականին հրատարակուած գիտական յօդուած
@hyw
2008 թվականին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@ast
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@en
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@nl
type
label
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@ast
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@en
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@nl
prefLabel
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@ast
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@en
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@nl
P2093
P2860
P1433
P1476
Inhibitory control over Ca(2+) ...... by mini-dystrophin expression
@en
P2093
Boris Martinac
Frederic V Wegner
Jeffrey S Chamberlain
Martin D H Teichmann
Oliver Friedrich
Rainer H A Fink
P2860
P356
10.1371/JOURNAL.PONE.0003644
P407
P577
2008-01-01T00:00:00Z