Survival motor neuron deficiency slows myoblast fusion through reduced myomaker and myomixer expression
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Title
Survival motor neuron deficiency slows myoblast fusion through reduced myomaker and myomixer expression
Authors
Keywords
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Journal
Journal of Cachexia Sarcopenia and Muscle
Volume 12, Issue 4, Pages 1098-1116
Publisher
Wiley
Online
2021-06-11
DOI
10.1002/jcsm.12740
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Note: Only part of the references are listed.- Muscle-specific SMN reduction reveals motor neuron–independent disease in spinal muscular atrophy models
- (2020) Jeong-Ki Kim et al. JOURNAL OF CLINICAL INVESTIGATION
- Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophy
- (2020) Haiyan Zhou et al. Journal of Cachexia Sarcopenia and Muscle
- Myocyte-derived Myomaker expression is required for regenerative fusion but exacerbates membrane instability in dystrophic myofibers
- (2020) Michael J. Petrany et al. JCI Insight
- Nusinersen in later-onset spinal muscular atrophy
- (2019) Basil T. Darras et al. NEUROLOGY
- Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study
- (2019) Darryl C. De Vivo et al. NEUROMUSCULAR DISORDERS
- Ethical guidelines for publishing in the Journal of Cachexia, Sarcopenia and Muscle : update 2019
- (2019) Stephan Haehling et al. Journal of Cachexia Sarcopenia and Muscle
- Nusinersen versus Sham Control in Later-Onset Spinal Muscular Atrophy
- (2018) Eugenio Mercuri et al. NEW ENGLAND JOURNAL OF MEDICINE
- Myoblast fusion confusion: the resolution begins
- (2018) Srihari C. Sampath et al. Skeletal Muscle
- Myomaker and Myomerger Work Independently to Control Distinct Steps of Membrane Remodeling during Myoblast Fusion
- (2018) Evgenia Leikina et al. DEVELOPMENTAL CELL
- Impaired myogenic development, differentiation and function in hESC-derived SMA myoblasts and myotubes
- (2018) Nicole Hellbach et al. PLoS One
- Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
- (2017) Jerry R. Mendell et al. NEW ENGLAND JOURNAL OF MEDICINE
- Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
- (2017) Richard S. Finkel et al. NEW ENGLAND JOURNAL OF MEDICINE
- Control of muscle formation by the fusogenic micropeptide myomixer
- (2017) Pengpeng Bi et al. SCIENCE
- The microprotein Minion controls cell fusion and muscle formation
- (2017) Qiao Zhang et al. Nature Communications
- Myomerger induces fusion of non-fusogenic cells and is required for skeletal muscle development
- (2017) Malgorzata E. Quinn et al. Nature Communications
- The role of the immunoproteasome in interferon-γ-mediated microglial activation
- (2017) Kasey E. Moritz et al. Scientific Reports
- Optimization of Morpholino Antisense Oligonucleotides Targeting the Intronic Repressor Element1 in Spinal Muscular Atrophy
- (2016) Erkan Y Osman et al. MOLECULAR THERAPY
- Differential induction of muscle atrophy pathways in two mouse models of spinal muscular atrophy
- (2016) Marc-Olivier Deguise et al. Scientific Reports
- Myomaker, Regulated by MYOD, MYOG and miR-140-3p, Promotes Chicken Myoblast Fusion
- (2015) Wen Luo et al. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
- Myomaker is essential for muscle regeneration
- (2014) Douglas P. Millay et al. GENES & DEVELOPMENT
- Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy
- (2014) Justin G. Boyer et al. HUMAN MOLECULAR GENETICS
- Survival motor neuron protein deficiency impairs myotube formation by altering myogenic gene expression and focal adhesion dynamics
- (2014) Katherine V. Bricceno et al. HUMAN MOLECULAR GENETICS
- Myomaker is a membrane activator of myoblast fusion and muscle formation
- (2013) Douglas P. Millay et al. NATURE
- Signaling Mechanisms in Mammalian Myoblast Fusion
- (2013) S. M. Hindi et al. Science Signaling
- More than a bystander: the contributions of intrinsic skeletal muscle defects in motor neuron diseases
- (2013) Justin G. Boyer et al. Frontiers in Physiology
- Early onset muscle weakness and disruption of muscle proteins in mouse models of spinal muscular atrophy
- (2013) Justin G Boyer et al. Skeletal Muscle
- Fasudil improves survival and promotes skeletal muscle development in a mouse model of spinal muscular atrophy
- (2012) Melissa Bowerman et al. BMC Medicine
- Turning on Myogenin in Muscle: A Paradigm for Understanding Mechanisms of Tissue-Specific Gene Expression
- (2012) Herve Faralli et al. COMPARATIVE AND FUNCTIONAL GENOMICS
- A cell-autonomous defect in skeletal muscle satellite cells expressing low levels of survival of motor neuron protein
- (2012) Monica Hayhurst et al. DEVELOPMENTAL BIOLOGY
- Histone deacetylase inhibition suppresses myogenin-dependent atrogene activation in spinal muscular atrophy mice
- (2012) Katherine V. Bricceno et al. HUMAN MOLECULAR GENETICS
- Survival Motor Neuron Protein in Motor Neurons Determines Synaptic Integrity in Spinal Muscular Atrophy
- (2012) T. L. Martinez et al. JOURNAL OF NEUROSCIENCE
- Muscles in a mouse model of spinal muscular atrophy show profound defects in neuromuscular development even in the absence of failure in neuromuscular transmission or loss of motor neurons
- (2011) Young il Lee et al. DEVELOPMENTAL BIOLOGY
- Reversible molecular pathology of skeletal muscle in spinal muscular atrophy
- (2011) Chantal A. Mutsaers et al. HUMAN MOLECULAR GENETICS
- Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy
- (2011) K. K. Y. Ling et al. HUMAN MOLECULAR GENETICS
- Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN
- (2010) Kevin D Foust et al. NATURE BIOTECHNOLOGY
- Impaired Synaptic Vesicle Release and Immaturity of Neuromuscular Junctions in Spinal Muscular Atrophy Mice
- (2009) L. Kong et al. JOURNAL OF NEUROSCIENCE
- Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?
- (2009) Arthur H. M. Burghes et al. NATURE REVIEWS NEUROSCIENCE
- Antisense Masking of an hnRNP A1/A2 Intronic Splicing Silencer Corrects SMN2 Splicing in Transgenic Mice
- (2008) Yimin Hua et al. AMERICAN JOURNAL OF HUMAN GENETICS
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