Cargando…

Nonmechanical Roles of Dystrophin and Associated Proteins in Exercise, Neuromuscular Junctions, and Brains

Dystrophin-glycoprotein complex (DGC) is an important structural unit in skeletal muscle that connects the cytoskeleton (f-actin) of a muscle fiber to the extracellular matrix (ECM). Several muscular dystrophies, such as Duchenne muscular dystrophy, Becker muscular dystrophy, congenital muscular dys...

Descripción completa

Detalles Bibliográficos
Autores principales:	Nichols, Bailey, Takeda, Shin’ichi, Yokota, Toshifumi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2015
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588140/ https://www.ncbi.nlm.nih.gov/pubmed/26230713 http://dx.doi.org/10.3390/brainsci5030275

Ejemplares similares

Restoring Dystrophin Expression in Duchenne Muscular Dystrophy: Current Status of Therapeutic Approaches
por: Shimizu-Motohashi, Yuko, et al.
Publicado: (2019)

α1-Syntrophin–deficient skeletal muscle exhibits hypertrophy and aberrant formation of neuromuscular junctions during regeneration
por: Hosaka, Yukio, et al.
Publicado: (2002)

Antisense PMO cocktails effectively skip dystrophin exons 45-55 in myotubes transdifferentiated from DMD patient fibroblasts
por: Lee, Joshua, et al.
Publicado: (2018)

A disease- and phosphorylation-related nonmechanical function for keratin 8
por: Ku, Nam-On, et al.
Publicado: (2006)

Multi-exon Skipping Using Cocktail Antisense Oligonucleotides in the Canine X-linked Muscular Dystrophy
por: Miskew Nichols, Bailey, et al.
Publicado: (2016)

Syncope, Near Syncope, or Nonmechanical Falls as a Presenting Feature of COVID-19
por: Chen, Tara, et al.
Publicado: (2020)

Rejuvenation of the aged neuromuscular junction by exercise
por: Kreko-Pierce, Tabita, et al.
Publicado: (2018)

Nonmechanical parfocal and autofocus features based on wave propagation distribution in lensfree holographic microscopy
por: Dharmawan, Agus Budi, et al.
Publicado: (2021)

The Ependymal Region Prevents Glioblastoma From Penetrating Into the Ventricle via a Nonmechanical Force
por: Li, Kaishu, et al.
Publicado: (2021)

The Neuromuscular Junction: Roles in Aging and Neuromuscular Disease
por: Iyer, Shama R., et al.
Publicado: (2021)

iNOS is not responsible for RyR1 S-nitrosylation in mdx mice with truncated dystrophin
por: Nogami, Ken’ichiro, et al.
Publicado: (2020)

Nonmechanical Infrared Beam Steering Using Blue Addressed Quantum Dot Doped Liquid Crystal Grating
por: Wang, Xiangru, et al.
Publicado: (2017)

Full-length human dystrophin on human artificial chromosome compensates for mouse dystrophin deficiency in a Duchenne muscular dystrophy mouse model
por: Hiramuki, Yosuke, et al.
Publicado: (2023)

Cardiac Involvement in Dystrophin-Deficient Females: Current Understanding and Implications for the Treatment of Dystrophinopathies
por: Lim, Kenji Rowel Q., et al.
Publicado: (2020)

Odontoid process metastasis of bronchial carcinoma as a rare cause for nonmechanical neck pain: a case report
por: Lakemeier, Stefan, et al.
Publicado: (2009)

Protein–lipid interplay at the neuromuscular junction
por: Unwin, Nigel
Publicado: (2022)

Molecular Diagnosis and Novel Therapies for Neuromuscular Diseases
por: Maruyama, Rika, et al.
Publicado: (2020)

Accumulation of Dystrophin-Positive Muscle Fibers and Improvement of Neuromuscular Junctions in mdx Mouse Muscles after Bone Marrow Transplantation under Different Conditions
por: Sokolova, Anastasiia V., et al.
Publicado: (2023)

Pharmacological activation of SERCA ameliorates dystrophic phenotypes in dystrophin-deficient mdx mice
por: Nogami, Ken'ichiro, et al.
Publicado: (2021)

Gene Expression Profile at the Motor Endplate of the Neuromuscular Junction of Fast-Twitch Muscle
por: Huang, Kun, et al.
Publicado: (2020)

Treatment with the anti-IL-6 receptor antibody attenuates muscular dystrophy via promoting skeletal muscle regeneration in dystrophin-/utrophin-deficient mice
por: Wada, Eiji, et al.
Publicado: (2017)

The importance of dystrophin and the dystrophin associated proteins in vascular smooth muscle
por: Kaplan, Katherine M., et al.
Publicado: (2022)

Splicing regulation of GFPT1 muscle-specific isoform and its roles in glucose metabolisms and neuromuscular junction
por: Farshadyeganeh, Paniz, et al.
Publicado: (2023)

The Role of Muscle microRNAs in Repairing the Neuromuscular Junction
por: Valdez, Gregorio, et al.
Publicado: (2014)

The role of Rapsyn in neuromuscular junction and congenital myasthenic syndrome
por: Liao, Xufeng, et al.
Publicado: (2023)

Localization of the DMDL gene-encoded dystrophin-related protein using a panel of nineteen monoclonal antibodies: presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles, and in proliferating brain cell lines
Publicado: (1991)

Characterization of brain dystrophins absence and impact in dystrophin-deficient Dmd(mdx) rat model
por: Caudal, Dorian, et al.
Publicado: (2020)

The Effects of Exercise-induced Fatigue on Acetylcholinesterase Expression and Activity at Rat Neuromuscular Junctions
por: Wen, Guo, et al.
Publicado: (2009)

The expression and function of gelatinolytic activity at the rat neuromuscular junction upon physical exercise
por: Yeghiazaryan, Marine, et al.
Publicado: (2014)

Morphological peculiarities of neuromuscular junctions among different fiber types: Effect of exercise
por: Seene, Teet, et al.
Publicado: (2017)

Effects of Nandrolone Decanoate on Skeletal Muscle and Neuromuscular Junction of Sedentary and Exercised Rats
por: Tibúrcio, Felipe Cantore, et al.
Publicado: (2023)

Reconstruction of the neuromuscular junction connectome
por: Srinivasan, Ranga, et al.
Publicado: (2010)

Axons Compete for Neuromuscular Junctions
por: Robinson, Richard
Publicado: (2012)

Autoimmune Channelopathies at Neuromuscular Junction
por: Huang, Kun, et al.
Publicado: (2019)

Long-Term Efficacy of Systemic Multiexon Skipping Targeting Dystrophin Exons 45–55 With a Cocktail of Vivo-Morpholinos in Mdx52 Mice
por: Echigoya, Yusuke, et al.
Publicado: (2015)

Diversity of the Brain Dystrophin-Glycoprotein Complex
por: Culligan, Kevin, et al.
Publicado: (2002)

Morpholino Oligomer-Induced Dystrophin Isoforms to Map the Functional Domains in the Dystrophin Protein
por: Li, Dunhui, et al.
Publicado: (2020)

Natural History of a Mouse Model Overexpressing the Dp71 Dystrophin Isoform
por: Lim, Kenji Rowel Q., et al.
Publicado: (2021)

Impaired regenerative capacity and lower revertant fibre expansion in dystrophin-deficient mdx muscles on DBA/2 background
por: Rodrigues, Merryl, et al.
Publicado: (2016)

Antisense PMO Found in Dystrophic Dog Model Was Effective in Cells from Exon 7-Deleted DMD Patient
por: Saito, Takashi, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_65qn41bujb7d0enoh0bf3o5oeo