标题
Dynamic neuromuscular remodeling precedes motor-unit loss in a mouse model of ALS
作者
关键词
-
出版物
eLife
Volume 7, Issue -, Pages -
出版商
eLife Sciences Publications, Ltd
发表日期
2018-10-15
DOI
10.7554/elife.41973
参考文献
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。- miR126-5p down-regulation facilitates axon degeneration and NMJ disruption via a non-cell-autonomous mechanism in ALS
- (2018) Roy Maimon et al. JOURNAL OF NEUROSCIENCE
- Preserving neuromuscular synapses in ALS by stimulating MuSK with a therapeutic agonist antibody
- (2018) Sarah Cantor et al. eLife
- Opposite Synaptic Alterations at the Neuromuscular Junction in an ALS Mouse Model: When Motor Units Matter
- (2017) Elsa Tremblay et al. JOURNAL OF NEUROSCIENCE
- The Role of Skeletal Muscle in Amyotrophic Lateral Sclerosis
- (2016) Jean-Philippe Loeffler et al. BRAIN PATHOLOGY
- Axonal degeneration, distal collateral branching and neuromuscular junction architecture alterations occur prior to symptom onset in the SOD1G93A mouse model of amyotrophic lateral sclerosis
- (2016) Jayden A. Clark et al. JOURNAL OF CHEMICAL NEUROANATOMY
- Immune response in peripheral axons delays disease progression in SOD1G93A mice
- (2016) Giovanni Nardo et al. Journal of Neuroinflammation
- Muscle Fibers Secrete FGFBP1 to Slow Degeneration of Neuromuscular Synapses during Aging and Progression of ALS
- (2016) Thomas Taetzsch et al. JOURNAL OF NEUROSCIENCE
- New perspectives on amyotrophic lateral sclerosis: the role of glial cells at the neuromuscular junction
- (2016) Danielle Arbour et al. JOURNAL OF PHYSIOLOGY-LONDON
- Branch-Specific Microtubule Destabilization Mediates Axon Branch Loss during Neuromuscular Synapse Elimination
- (2016) Monika S. Brill et al. NEURON
- Length-dependent axo-terminal degeneration at the neuromuscular synapses of type II muscle in SOD1 mice
- (2016) C. Tallon et al. NEUROSCIENCE
- Gamma motor neurons survive and exacerbate alpha motor neuron degeneration in ALS
- (2016) Melanie Lalancette-Hebert et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Prion-like propagation of mutant SOD1 misfolding and motor neuron disease spread along neuroanatomical pathways
- (2015) Jacob I. Ayers et al. ACTA NEUROPATHOLOGICA
- Elevated Mitochondrial Bioenergetics and Axonal Arborization Size Are Key Contributors to the Vulnerability of Dopamine Neurons
- (2015) Consiglia Pacelli et al. CURRENT BIOLOGY
- Early and Persistent Abnormal Decoding by Glial Cells at the Neuromuscular Junction in an ALS Model
- (2015) D. Arbour et al. JOURNAL OF NEUROSCIENCE
- A Computational Model of Motor Neuron Degeneration
- (2014) Gwendal Le Masson et al. NEURON
- Intercellular propagated misfolding of wild-type Cu/Zn superoxide dismutase occurs via exosome-dependent and -independent mechanisms
- (2014) Leslie I. Grad et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- ALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the disease
- (2014) Elizabeth B. Moloney et al. Frontiers in Neuroscience
- Enhancing Mitochondrial Calcium Buffering Capacity Reduces Aggregation of Misfolded SOD1 and Motor Neuron Cell Death without Extending Survival in Mouse Models of Inherited Amyotrophic Lateral Sclerosis
- (2013) P. A. Parone et al. JOURNAL OF NEUROSCIENCE
- Early Changes of Neuromuscular Transmission in the SOD1(G93A) Mice Model of ALS Start Long before Motor Symptoms Onset
- (2013) Mariana C. Rocha et al. PLoS One
- Characterization of early pathogenesis in the SOD1G93Amouse model of ALS: part II, results and discussion
- (2013) Sharon Vinsant et al. Brain and Behavior
- Selective knockdown of mutant SOD1 in Schwann cells ameliorates disease in G85R mutant SOD1 transgenic mice
- (2012) Lijun Wang et al. NEUROBIOLOGY OF DISEASE
- Increasing MuSK Activity Delays Denervation and Improves Motor Function in ALS Mice
- (2012) María J. Pérez-García et al. Cell Reports
- Changes in Aging Mouse Neuromuscular Junctions Are Explained by Degeneration and Regeneration of Muscle Fiber Segments at the Synapse
- (2011) Y. Li et al. JOURNAL OF NEUROSCIENCE
- Live imaging of amyotrophic lateral sclerosis pathogenesis: Disease onset is characterized by marked induction of GFAP in Schwann cells
- (2009) A. Florence Keller et al. GLIA
- Dismutase-competent SOD1 mutant accumulation in myelinating Schwann cells is not detrimental to normal or transgenic ALS model mice
- (2009) B. J. Turner et al. HUMAN MOLECULAR GENETICS
- Non–cell autonomous toxicity in neurodegenerative disorders: ALS and beyond
- (2009) Hristelina Ilieva et al. JOURNAL OF CELL BIOLOGY
- Schwann cells expressing dismutase active mutant SOD1 unexpectedly slow disease progression in ALS mice
- (2009) C. S. Lobsiger et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Activation of innate and humoral immunity in the peripheral nervous system of ALS transgenic mice
- (2009) I. M. Chiu et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Preferential motor unit loss in the SOD1G93Atransgenic mouse model of amyotrophic lateral sclerosis
- (2008) J. Hegedus et al. JOURNAL OF PHYSIOLOGY-LONDON
Become a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get StartedAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started