Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis.
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Mechanisms of Muscle Denervation in Aging: Insights from a Mouse Model of Amyotrophic Lateral SclerosisPostnatal muscle modification by myogenic factors modulates neuropathology and survival in an ALS mouse modelALS as a distal axonopathy: molecular mechanisms affecting neuromuscular junction stability in the presymptomatic stages of the diseaseA conditioning lesion provides selective protection in a rat model of Amyotrophic Lateral Sclerosis.Androgen receptors in muscle fibers induce rapid loss of force but not mass: implications for spinal bulbar muscular atrophy.Complement C5a-C5aR1 signalling drives skeletal muscle macrophage recruitment in the hSOD1G93A mouse model of amyotrophic lateral sclerosis.Skeletal muscle-restricted expression of human SOD1 causes motor neuron degeneration in transgenic miceShared resistance to aging and ALS in neuromuscular junctions of specific muscles.Early changes of neuromuscular transmission in the SOD1(G93A) mice model of ALS start long before motor symptoms onsetContractile dysfunction in muscle may underlie androgen-dependent motor dysfunction in spinal bulbar muscular atrophy.A metabolic switch toward lipid use in glycolytic muscle is an early pathologic event in a mouse model of amyotrophic lateral sclerosisEarly vulnerability to ischemia/reperfusion injury in motor terminals innervating fast muscles of SOD1-G93A mice.CLP1 links tRNA metabolism to progressive motor-neuron loss.A plural role for lipids in motor neuron diseases: energy, signaling and structure.Species-dependent neuropathology in transgenic SOD1 pigs.Amyotrophic lateral sclerosis and skeletal muscle: an update.The Role of Skeletal Muscle in Amyotrophic Lateral Sclerosis.New perspectives on amyotrophic lateral sclerosis: the role of glial cells at the neuromuscular junction.Mice Overexpressing Both Non-Mutated Human SOD1 and Mutated SOD1(G93A) Genes: A Competent Experimental Model for Studying Iron Metabolism in Amyotrophic Lateral Sclerosis.Slow myosin heavy chain expression in the absence of muscle activity.Altered in vitro proliferation of mouse SOD1-G93A skeletal muscle satellite cells.Compensatory plasticity in diaphragm and intercostal muscle utilization in a rat model of ALS.Dysregulation of microRNA biogenesis machinery and microRNA/RNA ratio in skeletal muscle of amyotrophic lateral sclerosis mice.Traumatic Brain Injury Results in Cellular, Structural and Functional Changes Resembling Motor Neuron Disease.Tweak regulates astrogliosis, microgliosis and skeletal muscle atrophy in a mouse model of amyotrophic lateral sclerosis.Sporadic amyotrophic lateral sclerosis (SALS) - skeletal muscle response to cerebrospinal fluid from SALS patients in a rat model.Phosphorylated TDP-43 (pTDP-43) aggregates in the axial skeletal muscle of patients with sporadic and familial amyotrophic lateral sclerosis.Neuromuscular dysfunction in the mutant superoxide dismutase mouse model of amyotrophic lateral sclerosis
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P2860
Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh-hant
name
Properties of slow- and fast-t ...... amyotrophic lateral sclerosis.
@en
Properties of slow- and fast-t ...... amyotrophic lateral sclerosis.
@nl
type
label
Properties of slow- and fast-t ...... amyotrophic lateral sclerosis.
@en
Properties of slow- and fast-t ...... amyotrophic lateral sclerosis.
@nl
prefLabel
Properties of slow- and fast-t ...... amyotrophic lateral sclerosis.
@en
Properties of slow- and fast-t ...... amyotrophic lateral sclerosis.
@nl
P2093
P1476
Properties of slow- and fast-t ...... amyotrophic lateral sclerosis
@en
P2093
Alvin K J Quah
Elizabeth Lopes
Jan M West
Rachel L Scott
Surindar S Cheema
P304
P356
10.1016/J.NMD.2005.02.005
P577
2005-05-01T00:00:00Z