AbstractDystrophin, which is absent in skeletal muscle of Duchenne muscular dystrophy patients, has not been considered to play a major structural role in the cell membrane of skeletal muscle because of its low abundance (∼ 0.002% of total muscle protein). Here, were have determined the relative abundance of dystrophin in a membrane cytoskeleton preparation and found that dystrophin constitutes approximately 5% of the total membrane cytoskeleton fraction of skeletal muscle sarcolemma. In addition, dystrophin can be removed from surcolemma by alkaline treatment. Thus, our results have demonstrated that dystrophin is a major component of the subsurcolemmal cytoskeleton in skeletal muscle and suggest that dystrophin could play a major structur...
Supramolecular membrane complexes of low abundance are difficult to study by routine bioanalytical t...
The almost complete loss of the membrane cytoskeletal protein dystrophin and concomitant drastic red...
The dystroglycan complex contains the transmembrane protein β-dystroglycan and its interacting extra...
Dystrophin is localized, in normal muscle fibers, on the cytoplasmic surface of the sarcolemma. The ...
Duchene muscular dystrophy (DMD)-is a lethal inherited disease, affecting 1 in 3500 boys. DMD is cha...
International audienceThe dystrophin-glycoprotein complex (DGC) is a large trans-sarcolemmal complex...
AbstractDuchenne muscular dystrophy is the most prevalent and severe form of human muscular dystroph...
Abstractβ-Dystroglycan is the central member of a transmembrane protein complex of the skeletal musc...
AbstractDuchenne muscular dystrophy (DMD) patients and mdx mice are characterized by the absence of ...
AbstractDue to its restricted localisation to the neuromuscular junction and based on sequence homol...
Dystrophin was purified by immunoaffinity chromatography from detergent-solubilized Torpedo electric...
The cell biological hypothesis of Duchenne muscular dystrophy assumes that deficiency in the membran...
The discovery of the dystrophin gene, whose mutations lead to Duchenne's and Becker's muscular dystr...
\ua9 2021 by the authors. Licensee MDPI, Basel, Switzerland. The systematic bioanalytical characteri...
Abstract. Dystrophin, the protein product of the hu-man Duchenne muscular dystrophy gene, exists in ...
Supramolecular membrane complexes of low abundance are difficult to study by routine bioanalytical t...
The almost complete loss of the membrane cytoskeletal protein dystrophin and concomitant drastic red...
The dystroglycan complex contains the transmembrane protein β-dystroglycan and its interacting extra...
Dystrophin is localized, in normal muscle fibers, on the cytoplasmic surface of the sarcolemma. The ...
Duchene muscular dystrophy (DMD)-is a lethal inherited disease, affecting 1 in 3500 boys. DMD is cha...
International audienceThe dystrophin-glycoprotein complex (DGC) is a large trans-sarcolemmal complex...
AbstractDuchenne muscular dystrophy is the most prevalent and severe form of human muscular dystroph...
Abstractβ-Dystroglycan is the central member of a transmembrane protein complex of the skeletal musc...
AbstractDuchenne muscular dystrophy (DMD) patients and mdx mice are characterized by the absence of ...
AbstractDue to its restricted localisation to the neuromuscular junction and based on sequence homol...
Dystrophin was purified by immunoaffinity chromatography from detergent-solubilized Torpedo electric...
The cell biological hypothesis of Duchenne muscular dystrophy assumes that deficiency in the membran...
The discovery of the dystrophin gene, whose mutations lead to Duchenne's and Becker's muscular dystr...
\ua9 2021 by the authors. Licensee MDPI, Basel, Switzerland. The systematic bioanalytical characteri...
Abstract. Dystrophin, the protein product of the hu-man Duchenne muscular dystrophy gene, exists in ...
Supramolecular membrane complexes of low abundance are difficult to study by routine bioanalytical t...
The almost complete loss of the membrane cytoskeletal protein dystrophin and concomitant drastic red...
The dystroglycan complex contains the transmembrane protein β-dystroglycan and its interacting extra...