Desmin and vimentin are two intermediate filaments, abundant in fetal skeletal nuscle, ahnost undetectable in mature skeletal muscle which increase in regenerating and partially damaged skeletal muscle fibers. To determine their content in neuromuscular disorders immunohistochemical studies of desmin and vimentin were performed on 53 human nuscle specimens . The labelled streptavidin biotin technique (DAKO, LSAB Kit, alkaline phosphatase) was used. Strong staining intensity was seen in regenerating and partially damaged fibers of inflammatory myopathies and muscular dystrophy. Necrotic fibers lost their reactivity for both filaments. Type II glycogenosis showed an increased reactivity for desmin and vimentin. A mild increase in desmin and...
We used immunohistochemistry to study the expression of some proteins of the cytoskeleton (desmin an...
Mice lacking desmin produce muscle fibers with Z disks and normal sarcomeric organization. However, ...
The Protein Surplus Myopathies (PSM) are characterized by accumulation of protein aggregates, ident...
The developmental status of muscle fibers was investigated in three cases of myotubular myopathy: on...
Abstract--Expression patterns of the intermediate filament proteins (IFPs) desmin and vimentin, in b...
An expression vector was prepared containing a cDNA coding for a truncated version of the intermedia...
Desmin is the intermediate filament (IF) protein occurring exclusively in muscle and endothelial cel...
The muscle fibre cytoskeleton of skeletal and heart muscle cells is composed mainly of intermediate ...
We investigated the immunohistochemical distribution of cytoskeletal proteins in smooth muscles of 1...
Muscular dystrophies are a heterogeneous group of genetically determined progressive disorders of th...
PURPOSE. To investigate whether the distribution of intermediate filament protein desmin is related ...
We examined by immunofluorescence the distribution of vimentin, desmin, α-smooth muscle actin and α-...
Autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) is one of a number of allelic disorde...
Desmin is a type III intermediate filament protein found in the cytoskeleton of skeletal muscle. Mut...
Many biochemical studies on skeletal muscle have been reported in experimental muscular dystrophy of...
We used immunohistochemistry to study the expression of some proteins of the cytoskeleton (desmin an...
Mice lacking desmin produce muscle fibers with Z disks and normal sarcomeric organization. However, ...
The Protein Surplus Myopathies (PSM) are characterized by accumulation of protein aggregates, ident...
The developmental status of muscle fibers was investigated in three cases of myotubular myopathy: on...
Abstract--Expression patterns of the intermediate filament proteins (IFPs) desmin and vimentin, in b...
An expression vector was prepared containing a cDNA coding for a truncated version of the intermedia...
Desmin is the intermediate filament (IF) protein occurring exclusively in muscle and endothelial cel...
The muscle fibre cytoskeleton of skeletal and heart muscle cells is composed mainly of intermediate ...
We investigated the immunohistochemical distribution of cytoskeletal proteins in smooth muscles of 1...
Muscular dystrophies are a heterogeneous group of genetically determined progressive disorders of th...
PURPOSE. To investigate whether the distribution of intermediate filament protein desmin is related ...
We examined by immunofluorescence the distribution of vimentin, desmin, α-smooth muscle actin and α-...
Autosomal dominant Emery-Dreifuss muscular dystrophy (AD-EDMD) is one of a number of allelic disorde...
Desmin is a type III intermediate filament protein found in the cytoskeleton of skeletal muscle. Mut...
Many biochemical studies on skeletal muscle have been reported in experimental muscular dystrophy of...
We used immunohistochemistry to study the expression of some proteins of the cytoskeleton (desmin an...
Mice lacking desmin produce muscle fibers with Z disks and normal sarcomeric organization. However, ...
The Protein Surplus Myopathies (PSM) are characterized by accumulation of protein aggregates, ident...