نتایج جستجو برای: muscular dystrophies

تعداد نتایج: 45375  

2013
Sonia Paco Susana G. Kalko Cristina Jou María A. Rodríguez Joan Corbera Francesco Muntoni Lucy Feng Eloy Rivas Ferran Torner Francesca Gualandi Anna M. Gomez-Foix Anna Ferrer Carlos Ortez Andrés Nascimento Jaume Colomer Cecilia Jimenez-Mallebrera

Ullrich congenital muscular dystrophy (UCMD), caused by collagen VI deficiency, is a common congenital muscular dystrophy. At present, the role of collagen VI in muscle and the mechanism of disease are not fully understood. To address this we have applied microarrays to analyse the transcriptome of UCMD muscle and compare it to healthy muscle and other muscular dystrophies. We identified 389 ge...

Journal: :Anesthesia and analgesia 2009
Harshad Gurnaney Amanda Brown Ronald S Litman

BACKGROUND Patients with muscular dystrophy have been reported to experience a variety of life-threatening complications during and after general anesthesia. We performed a systematic analysis to define the spectrum of anesthetic-related complications in patients with muscular dystrophy, with an emphasis on malignant hyperthermia susceptibility. METHODS A literature search was undertaken usin...

2017
Leigh B. Waddell Frances J. Evesson Kathryn N. North Sandra T. Cooper Nigel F. Clarke

Journal: :Muscle & nerve 2000
R D Cohn K P Campbell

Muscular dystrophies represent a heterogeneous group of disorders, which have been largely classified by clinical phenotype. In the last 10 years, identification of novel skeletal muscle genes including extracellular matrix, sarcolemmal, cytoskeletal, cytosolic, and nuclear membrane proteins has changed the phenotype-based classification and shed new light on the molecular pathogenesis of these...

Journal: :Biological & pharmaceutical bulletin 2003
Tamao Endo Tatsushi Toda

Mammalian cells produce many glycoproteins, i.e., proteins with covalently attached sugar chains. Recent advances in glycobiology have revealed the importance of sugar chains as biosignals for multi-cellular organisms including cell-cell communication, intracellular signaling, protein folding, and targeting of proteins within cells. The O-mannosyl linkage, which used to be considered specific t...

Journal: :Molecules 2015
Leonidas A Phylactou

Muscular dystrophies are a heterogeneous group of inherited diseases with different molecular basss, but sharing similar clinical features and dystrophic changes.

2016

Duchenne muscular dystrophy mouse models have a predictable and reproducible time course of cardiomyopathy progression with discrete pathogenic steps, which closely parallel what we know occurs in the cardiomyopathy of patients with Duchenne muscular dystrophy. The slow progression of early pathogenic steps common to many cardiomyopathies may make Duchenne muscular dystrophy models useful for i...

Journal: :Seminars in cell & developmental biology 2017
Antonio L Serrano Pura Muñoz-Cánoves

Duchenne muscular dystrophy (DMD) is one of the most devastating neuromuscular genetic diseases caused by the absence of dystrophin. The continuous episodes of muscle degeneration and regeneration in dystrophic muscle are accompanied by chronic inflammation and fibrosis deposition, which exacerbate disease progression. Thus, in addition of investigating strategies to cure the primary defect by ...

Journal: :Stem cells 2012
Martina Piccoli Chiara Franzin Enrica Bertin Luca Urbani Bert Blaauw Andrea Repele Elisa Taschin Angelo Cenedese Giovanni Franco Zanon Isabelle André-Schmutz Antonio Rosato Judith Melki Marina Cavazzana-Calvo Michela Pozzobon Paolo De Coppi

Mutations in the survival of motor neuron gene (SMN1) are responsible for spinal muscular atrophy, a fatal neuromuscular disorder. Mice carrying a homozygous deletion of Smn exon 7 directed to skeletal muscle (HSA-Cre, Smn(F7/F7) mice) present clinical features of human muscular dystrophies for which new therapeutic approaches are highly warranted. Herein we demonstrate that tail vein transplan...

Journal: :The Journal of clinical investigation 2015
Marco Sandri

Muscular dystrophies are monogenetic diseases that are often characterized by the degeneration of both cardiac and skeletal muscle. Gene therapy to correct the mutated gene has shown promise in both animal models and clinical trials; however, current gene delivery strategies are limited to the introduction of the corrected gene into only one tissue. Strategies to target multiple striated muscle...

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