Results 251 to 260 of about 57,573 (289)
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Desmin

1999
Abstract Desmin belongs to the intermediate filament family of proteins. Protein sequence homology and intron placement of the desmin gene classify desmin as a type Ill IF protein, together with vimentin, peripherin, and giial fibrillary acidic protein.
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Desmin‐related neuromuscular disorders

Muscle & Nerve, 1995
AbstractDesmin, the intermediate filament protein of skeletal muscle fibers, cardiac myocytes, and certain smooth muscle cells, is a member of the cytoskeleton linking Z‐bands with the plasmalemma and the nucleus. The pathology of desmin in human neuromuscular disorders is always marked by increased amounts, diffusely or focally.
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Desmin pathology in neuromuscular diseases

Virchows Archiv B Cell Pathology Including Molecular Pathology, 1993
Desmin is an intermediate filament protein that in striated muscle is normally located at Z-bands, beneath the sarcolemma, and prominently at neuromuscular junctions. It is abundant during myogenesis and in regenerating fibers, but decreases in amount with maturation; in regenerating and denervated muscle fibers it is co-expressed with vimentin ...
H H, Goebel, A, Bornemann
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Desmin mutations in the terminal consensus motif prevent synemin-desmin heteropolymer filament assembly

Experimental Cell Research, 2011
Disorganization of the desmin network is associated with cardiac and skeletal myopathies characterized by accumulation of desmin-containing aggregates in the cells. Multiple associations of intermediate filament proteins form a network to increase mechanical and functional stability. Synemin is a desmin-associated type VI intermediate filament protein.
Chourbagi O.   +6 more
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[Desmin-related cardiomyopathy].

Arkhiv patologii, 2011
The observation of 26 years old patient with desminopathy declared itself by hypertrophied cardiomyopathy with its transformation into restrictive phenotype is presented. The features of pathologic course at the patient were a dominance and diversity of cardiac manifestations.
M G, Rybakova   +4 more
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Structural and functional analysis of a new desmin variant causing desmin-related myopathy.

Human mutation, 2001
Desmin-related myopathy is a familial or sporadic disease characterized by skeletal muscle weakness and cardiomyopathy as well as the presence of intracytoplasmic aggregates of desmin-reactive material in the muscle cells. Previously, two kinds of deletions and eight missense mutations have been identified in the desmin gene and proven to be ...
Goudeau, Bertrand   +8 more
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New roles for desmin in the maintenance of muscle homeostasis

FEBS Journal, 2022
Harald Herrmann, Shenhav Cohen
exaly  

Desmin

1998
Tak W. Mak   +4 more
openaire   +1 more source

Desmin-370

Drugs of the Future, 1994
G. Tamagnone, M. Barbanti
openaire   +1 more source

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