نتایج جستجو برای: myofibrillar myopathy

تعداد نتایج: 14255  

Journal: :International Journal of Molecular Sciences 2023

Myofibrillar myopathies (MFMs) are a group of hereditary neuromuscular disorders sharing common histological features, such as myofibrillar derangement, Z-disk disintegration, and the accumulation degradation products into protein aggregates. They caused by mutations in several genes that encode either structural proteins or molecular chaperones. Nevertheless, mechanisms which mutated result ag...

2016
Teet Seene Priit Kaasik

Muscle weakness in corticosteroid myopathy is mainly the result of the destruction and atrophy of the myofibrillar compartment of fast-twitch muscle fibers. Decrease of titin and myosin, and the ratio of nebulin and MyHC in myopathic muscle, shows that these changes of contractile and elastic proteins are the result of increased catabolism of the abovementioned proteins in skeletal muscle. Slow...

Journal: :Brain : a journal of neurology 2012
Monica Ohlsson Carola Hedberg Björn Brådvik Christopher Lindberg Homa Tajsharghi Olof Danielsson Atle Melberg Bjarne Udd Tommy Martinsson Anders Oldfors

Hereditary myopathy with early respiratory failure and extensive myofibrillar lesions has been described in sporadic and familial cases and linked to various chromosomal regions. The mutated gene is unknown in most cases. We studied eight individuals, from three apparently unrelated families, with clinical and pathological features of hereditary myopathy with early respiratory failure. The inve...

Journal: :Neuropathology and applied neurobiology 2011
J A Bevilacqua N Monnier M Bitoun B Eymard A Ferreiro S Monges F Lubieniecki A L Taratuto A Laquerrière K G Claeys I Marty M Fardeau P Guicheney J Lunardi N B Romero

AIMS To report the clinical, pathological and genetic findings in a group of patients with a previously not described phenotype of congenital myopathy due to recessive mutations in the gene encoding the type 1 muscle ryanodine receptor channel (RYR1). METHODS Seven unrelated patients shared a predominant axial and proximal weakness of varying severity, with onset during the neonatal period, a...

2007
Rolf Schröder Alexandra Vrabie Hans H Goebel

Mutations of the human desmin gene on chromosome 2q35 cause a familial or sporadic form of skeletal myopathy frequently associated with cardiac abnormalities. Skeletal and cardiac muscle from patients with primary desminopathies characteristically display cytoplasmic accumulation of desmin-immunoreactive material and myofibrillar changes. However, desmin-positive protein aggregates in conjuncti...

Journal: :The Biochemical journal 2011
Pernilla von Nandelstadh Rabah Soliymani Marc Baumann Olli Carpen

MFM (myofibrillar myopathies) are caused by mutations in several sarcomeric components, including the Z-disc protein myotilin. The morphological changes typical of MFM include Z-disc alterations and aggregation of dense filamentous sarcomeric material. The causes and mechanisms of protein aggregation in myotilinopathies and other forms of MFM remain unknown, although impaired degradation may ex...

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