Torn apart: membrane rupture in muscular dystrophies and associated cardiomyopathies

scientific article published on July 2007

Torn apart: membrane rupture in muscular dystrophies and associated cardiomyopathies is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1172/JCI32686
P932PMC publication ID1904332
P698PubMed publication ID17607350

P2093author name stringRichard T Lee
Jan Lammerding
P2860cites workMyoferlin, a candidate gene and potential modifier of muscular dystrophyQ22010963
Loss of A-type lamin expression compromises nuclear envelope integrity leading to muscular dystrophyQ24681029
Defective membrane repair in dysferlin-deficient muscular dystrophyQ28203095
Abnormal nuclear shape and impaired mechanotransduction in emerin-deficient cellsQ28268495
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyQ28281738
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2BQ28281749
In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patientsQ30478576
Cardiac involvement in Emery-Dreifuss muscular dystrophyQ33152322
Dysferlin and the plasma membrane repair in muscular dystrophyQ33201061
Plasma Membrane Disruption: Repair, Prevention, AdaptationQ34271469
A clamping mechanism involved in SNARE-dependent exocytosisQ34541145
The heart in human dystrophinopathiesQ35067344
Nuclear envelope proteins and neuromuscular diseasesQ35093315
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction.Q35632054
Disruptions of muscle fiber plasma membranes. Role in exercise-induced damageQ35831693
Dysferlin-mediated membrane repair protects the heart from stress-induced left ventricular injuryQ35865366
LaminopathiesQ35923554
An emergency response team for membrane repairQ36146942
Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin geneQ40893835
Dystrophic heart failure blocked by membrane sealant poloxamerQ46604988
Ultrastructural abnormality of sarcolemmal nuclei in Emery-Dreifuss muscular dystrophy (EDMD).Q47699129
Poloxamer 188 failed to prevent exercise-induced membrane breakdown in mdx skeletal muscle fibers.Q50473991
Decreased mechanical stiffness in LMNA-/- cells is caused by defective nucleo-cytoskeletal integrity: implications for the development of laminopathies.Q51616068
Loss of cytoplasmic basic fibroblast growth factor from physiologically wounded myofibers of normal and dystrophic muscle.Q52515753
Lamins A and C but not lamin B1 regulate nuclear mechanics.Q53613002
Architectural abnormalities in muscle nuclei. Ultrastructural differences between X-linked and autosomal dominant forms of EDMDQ73366593
Pharmacokinetics of RheothRx injection in healthy male volunteersQ73533574
Nuclear sequestration of delta-sarcoglycan disrupts the nuclear localization of lamin A/C and emerin in cardiomyocytesQ79428627
P433issue7
P407language of work or nameEnglishQ1860
P304page(s)1749-1752
P577publication date2007-07-01
P1433published inJournal of Clinical InvestigationQ3186904
P1476titleTorn apart: membrane rupture in muscular dystrophies and associated cardiomyopathies
P478volume117

Reverse relations

cites work (P2860)
Q34118633Biochemical markers of muscular damage
Q93384433Cardiac MRI biomarkers for Duchenne muscular dystrophy
Q34497771Caveolae protect endothelial cells from membrane rupture during increased cardiac output
Q56981953Dysferlin, dystrophy, and dilatative cardiomyopathy
Q90634574Heart disease in a mutant mouse model of spontaneous eosinophilic myocarditis maps to three loci
Q42209023Muscle membrane repair and inflammatory attack in dysferlinopathy.
Q49704946Nuclear envelope proteins Nesprin2 and LaminA regulate proliferation and apoptosis of vascular endothelial cells in response to shear stress
Q46801990Qualitative electron microscopic analysis of cultured chick embryonic cardiac and skeletal muscle cells: the cellular effect of coenzyme q10 after exposure to triton x-100.
Q48695970The susceptibility to experimental autoimmune encephalomyelitis is not related to dysferlin-deficiency

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