相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Skeletal muscle: A review of molecular structure and function, in health and disease
Kavitha Mukund et al.
WILEY INTERDISCIPLINARY REVIEWS-SYSTEMS BIOLOGY AND MEDICINE (2020)
Keratin 18 is an integral part of the intermediate filament network in murine skeletal muscle
Joaquin M. Muriel et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2020)
Exercise-induced oxidative stress: Friend or foe?
Scott K. Powers et al.
JOURNAL OF SPORT AND HEALTH SCIENCE (2020)
Microtubule Plus End Dynamics - Do We Know How Microtubules Grow? Cells boost microtubule growth by promoting distinct structural transitions at growing microtubule ends
Jeffrey van Haren et al.
BIOESSAYS (2019)
The potential of utrophin and dystrophin combination therapies for Duchenne muscular dystrophy
Simon Guiraud et al.
HUMAN MOLECULAR GENETICS (2019)
Dystrophinopathy-associated dysfunction of Krebs cycle metabolism
Angus Lindsay et al.
HUMAN MOLECULAR GENETICS (2019)
The PRIDE database and related tools and resources in 2019: improving support for quantification data
Yasset Perez-Riverol et al.
NUCLEIC ACIDS RESEARCH (2019)
Mitochondrial content is preserved throughout disease progression in the mdx mouse model of Duchenne muscular dystrophy, regardless of taurine supplementation
Robert G. Barker et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2018)
Systemic AAV Micro-dystrophin Gene Therapy for Duchenne Muscular Dystrophy
Dongsheng Duan
MOLECULAR THERAPY (2018)
Striated muscle activator of Rho signalling (STARS) is reduced in ageing human skeletal muscle and targeted by miR-628-5p
A. P. Russell et al.
ACTA PHYSIOLOGICA (2017)
Progress toward Gene Therapy for Duchenne Muscular Dystrophy
Joel R. Chamberlain et al.
MOLECULAR THERAPY (2017)
Delayed onset of ambulation in boys with Duchenne muscular dystrophy: Potential use as an endpoint in clinical trials
Jacob J. Gissy et al.
NEUROMUSCULAR DISORDERS (2017)
Reduced nuclear translocation of serum response factor is associated with skeletal muscle atrophy in a cigarette smoke-induced mouse model of COPD
Ran Ma et al.
INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE (2017)
Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy
Jerry R. Mendell et al.
ANNALS OF NEUROLOGY (2016)
SWATH Mass Spectrometry Performance Using Extended Peptide MS/MS Assay Libraries
Jemma X. Wu et al.
MOLECULAR & CELLULAR PROTEOMICS (2016)
ABSENCE OF DYSTROPHIN DISRUPTS SKELETAL MUSCLE SIGNALING: ROLES OF Ca2+, REACTIVE OXYGEN SPECIES, AND NITRIC OXIDE IN THE DEVELOPMENT OF MUSCULAR DYSTROPHY
David G. Allen et al.
PHYSIOLOGICAL REVIEWS (2016)
Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy
Jarrod E. Church et al.
EXPERIMENTAL PHYSIOLOGY (2014)
ATALUREN TREATMENT OF PATIENTS WITH NONSENSE MUTATION DYSTROPHINOPATHY
Katharine Bushby et al.
MUSCLE & NERVE (2014)
Defects in Mitochondrial ATP Synthesis in Dystrophin-Deficient Mdx Skeletal Muscles May Be Caused by Complex I Insufficiency
Emma Rybalka et al.
PLOS ONE (2014)
Keratin 76 Is Required for Tight Junction Function and Maintenance of the Skin Barrier
Tia DiTommaso et al.
PLOS GENETICS (2014)
Micro-dystrophin and follistatin co-delivery restores muscle function in aged DMD model
Louise R. Rodino-Klapac et al.
HUMAN MOLECULAR GENETICS (2013)
Effect of resistance exercise contraction mode and protein supplementation on members of the STARS signalling pathway
Kristian Vissing et al.
JOURNAL OF PHYSIOLOGY-LONDON (2013)
Regulation of miRNAs in human skeletal muscle following acute endurance exercise and short-term endurance training
Aaron P. Russell et al.
JOURNAL OF PHYSIOLOGY-LONDON (2013)
Evidence-Based Path to Newborn Screening for Duchenne Muscular Dystrophy
Jerry R. Mendell et al.
ANNALS OF NEUROLOGY (2012)
Rudhira/BCAS3 is a cytoskeletal protein that controls Cdc42 activation and directional cell migration during angiogenesis
Mamta Jain et al.
EXPERIMENTAL CELL RESEARCH (2012)
Influences of Desmin and Keratin 19 on Passive Biomechanical Properties of Mouse Skeletal Muscle
Sameer B. Shah et al.
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY (2012)
Hsp72 preserves muscle function and slows progression of severe muscular dystrophy
Stefan M. Gehrig et al.
NATURE (2012)
Rapid Determination of Myosin Heavy Chain Expression in Rat, Mouse, and Human Skeletal Muscle Using Multicolor Immunofluorescence Analysis
Darin Bloemberg et al.
PLOS ONE (2012)
Striated muscle activator of Rho signalling (STARS) is a PGC-1α/oestrogen-related receptor-α target gene and is upregulated in human skeletal muscle after endurance exercise
Marita A. Wallace et al.
JOURNAL OF PHYSIOLOGY-LONDON (2011)
Actin-Binding Rho Activating Protein (Abra) Is Essential for Fluid Shear Stress-Induced Arteriogenesis
Kerstin Troidl et al.
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY (2009)
RhoA leads to up-regulation and relocalization of utrophin in muscle fibers
Cecile Gauthier-Rouviere et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2009)
Mutations and Polymorphisms of the Skeletal Muscle α-Actin Gene (ACTA1)
Nigel G. Laing et al.
HUMAN MUTATION (2009)
Rapid muscle atrophy response to unloading: pretranslational processes involving MHC and actin
Julia M. Giger et al.
JOURNAL OF APPLIED PHYSIOLOGY (2009)
Regulation of STARS and its downstream targets suggest a novel pathway involved in human skeletal muscle hypertrophy and atrophy
Severine Lamon et al.
JOURNAL OF PHYSIOLOGY-LONDON (2009)
PRECLINICAL DRUG TRIALS IN THE mdx MOUSE: ASSESSMENT OF RELIABLE AND SENSITIVE OUTCOME MEASURES
Christopher F. Spurney et al.
MUSCLE & NERVE (2009)
Adaptive and nonadaptive responses to voluntary wheel running by mdx mice
Rachel M. Landisch et al.
MUSCLE & NERVE (2008)
Prevention of muscle fibrosis and improvement in muscle performance in the mdx mouse by halofuginone
Tidhar Turgeman et al.
NEUROMUSCULAR DISORDERS (2008)
Effect of destrin mutations on the gene expression profile in vivo
Angela M. Verdoni et al.
PHYSIOLOGICAL GENOMICS (2008)
Absence of keratin 19 in mice causes skeletal myopathy with mitochondrial and sarcolemmal reorganization
Michele R. StoneO et al.
JOURNAL OF CELL SCIENCE (2007)
Two novel members of the ABLIM protein family, ABLIM-2 and -3, associate with STARS and directly bind F-actin
Tomasa Barrientos et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2007)
Nemaline myopathy caused by absence of α-skeletal muscle actin
Kristen J. Nowak et al.
ANNALS OF NEUROLOGY (2007)
Serum response factor: master regulator of the actin cytoskeleton and contractile apparatus
Joseph M. Miano et al.
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY (2007)
Phenotypic improvement of dystrophic muscles by rAAV/microdystrophin vectors is augmented by Igf1 codelivery
S Abmayr et al.
MOLECULAR THERAPY (2005)
Temporal gene expression profiling of dystrophin-deficient (mdx) mouse diaphragm identifies conserved and muscle group-specific mechanisms in the pathogenesis of muscular dystrophy
JD Porter et al.
HUMAN MOLECULAR GENETICS (2004)
The SRF target gene Fhl2 antagonizes RhoA/MAL-dependent activation of SRF
U Philippar et al.
MOLECULAR CELL (2004)
Histological parameters for the quantitative assessment of muscular dystrophy in the mdx-mouse
A Briguet et al.
NEUROMUSCULAR DISORDERS (2004)
Cloning and characterization of cytokeratins 8 and 19 in adult rat striated muscle - Interaction with the dystrophin glycoprotein complex
JA Ursitti et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2004)
STARS, a striated muscle activator of Rho signaling and serum response factor-dependent transcription
A Arai et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2002)
Function and genetics of dystrophin and dystrophin-related proteins in muscle
DJ Blake et al.
PHYSIOLOGICAL REVIEWS (2002)
Identification of a novel member of the chloride intracellular channel gene family (CLIC5) that associates with the actin cytoskeleton of placental microvilli
M Berryman et al.
MOLECULAR BIOLOGY OF THE CELL (2000)