Preferential motor unit loss in the SOD1 G93A transgenic mouse model of amyotrophic lateral sclerosis (Q81243139)

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scientific article published on 08 May 2008

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English	Preferential motor unit loss in the SOD1 G93A transgenic mouse model of amyotrophic lateral sclerosis	scientific article published on 08 May 2008

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scholarly article

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Europe PubMed Central

PubMed publication ID

18467368

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

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title

Preferential motor unit loss in the SOD1 G93A transgenic mouse model of amyotrophic lateral sclerosis (English)

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Europe PubMed Central

PubMed publication ID

18467368

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

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7 January 2020

main subject

amyotrophic lateral sclerosis

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author name string

J Hegedus

series ordinal

1

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Europe PubMed Central

PubMed publication ID

18467368

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

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C T Putman

series ordinal

2

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Europe PubMed Central

PubMed publication ID

18467368

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

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N Tyreman

series ordinal

3

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Europe PubMed Central

PubMed publication ID

18467368

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

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T Gordon

series ordinal

4

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Europe PubMed Central

PubMed publication ID

18467368

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publication date

8 May 2008

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Europe PubMed Central

PubMed publication ID

18467368

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

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7 January 2020

number of pages

15

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published in

Journal of Physiology

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Europe PubMed Central

PubMed publication ID

18467368

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volume

586

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Europe PubMed Central

PubMed publication ID

18467368

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issue

14

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Europe PubMed Central

PubMed publication ID

18467368

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7 January 2020

page(s)

3337-3351

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Europe PubMed Central

PubMed publication ID

18467368

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

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7 January 2020

cites work

Skeletal muscle fiber function and rate of disease progression in amyotrophic lateral sclerosis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Effect of exercise on stability of chronically enlarged motor units

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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AMPK activation increases uncoupling protein-3 expression and mitochondrial enzyme activities in rat muscle without fibre type transitions

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Sexual differences in onset of disease and response to exercise in a transgenic model of ALS

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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Hyperexcitability of cultured spinal motoneurons from presymptomatic ALS mice.

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PubMed

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12 December 2020

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Amyotrophic lateral sclerosis is a distal axonopathy: evidence in mice and man

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Mechanisms controlling axonal sprouting at the neuromuscular junction

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PubMed

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12 December 2020

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Adaptive and maladaptive motor axonal sprouting in aging and motoneuron disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Effects of strength, endurance and combined training on myosin heavy chain content and fibre-type distribution in humans

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Functional compensation in partially denervated muscles

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Terminal innervation ratio in neuromuscular disease. II. Disorders of lower motor neuron, peripheral nerve, and muscle

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Pattern of recruiting human motor units in neuropathies and motor neurone disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Contractile and electrical properties of human motor units in neuropathies and motor neurone disease

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Some electrical properties of motor units and their effects on the methods of estimating motor unit numbers

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Specific effects of low-frequency stimulation upon energy metabolism in tibialis anterior muscles of mouse, rat, guinea pig and rabbit.

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Three myosin heavy chain isoforms in type 2 skeletal muscle fibres.

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PubMed

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12 December 2020

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EMG patterns of rat ankle extensors and flexors during treadmill locomotion and swimming

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12 December 2020

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The histochemical profiles of fast fiber types IIB, IID, and IIA in skeletal muscles of mouse, rat, and rabbit

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Erratum: Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Morphological changes during fiber type transitions in low-frequency-stimulated rat fast-twitch muscle

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PubMed

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12 December 2020

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Does muscle reinnervation produce electromechanical dissociation in amyotrophic lateral sclerosis?

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12 December 2020

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Age-dependent penetrance of disease in a transgenic mouse model of familial amyotrophic lateral sclerosis

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Self-reinnervated cat medial gastrocnemius muscles. II. analysis of the mechanisms and significance of fiber type grouping in reinnervated muscles.

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Neuromuscular function impairment is not caused by motor neurone loss in FALS mice: an electromyographic study

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Progressive motor neuron impairment in an animal model of familial amyotrophic lateral sclerosis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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Fast-to-slow conversion following chronic low-frequency activation of medial gastrocnemius muscle in cats. I. Muscle and motor unit properties.

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https://pubmed.ncbi.nlm.nih.gov/18467368

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Coordinated expression of myosin heavy chain isoforms and metabolic enzymes within overloaded rat muscle fibers

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Functional properties of motor units in motor neuron diseases and neuropathies

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

based on heuristic

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Mice lacking cytosolic copper/zinc superoxide dismutase display a distinctive motor axonopathy

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Chronic low-frequency stimulation upregulates uncoupling protein-3 in transforming rat fast-twitch skeletal muscle

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Properties of slow- and fast-twitch muscle fibres in a mouse model of amyotrophic lateral sclerosis.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Gait analysis detects early changes in transgenic SOD1(G93A) mice

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PubMed

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12 December 2020

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A compensatory subpopulation of motor neurons in a mouse model of amyotrophic lateral sclerosis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

based on heuristic

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Selective vulnerability and pruning of phasic motoneuron axons in motoneuron disease alleviated by CNTF

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Altered axonal excitability properties in amyotrophic lateral sclerosis: impaired potassium channel function related to disease stage

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

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Effect of satellite cell ablation on low-frequency-stimulated fast-to-slow fibre-type transitions in rat skeletal muscle

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12 December 2020

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The expression of the chemorepellent Semaphorin 3A is selectively induced in terminal Schwann cells of a subset of neuromuscular synapses that display limited anatomical plasticity and enhanced vulnerability in motor neuron disease

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

based on heuristic

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Increased nodal persistent Na+ currents in human neuropathy and motor neuron disease estimated by latent addition

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

based on heuristic

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Method for counting motor units in mice and validation using a mathematical model.

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/18467368

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12 December 2020

based on heuristic

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Time course of preferential motor unit loss in the SOD1 G93A mouse model of amyotrophic lateral sclerosis

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12 December 2020

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Early and selective loss of neuromuscular synapse subtypes with low sprouting competence in motoneuron diseases

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12 December 2020

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From Charcot to SOD1: mechanisms of selective motor neuron death in ALS.

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12 December 2020

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Early detection of denervated muscle fibers in hindlimb muscles after sciatic nerve transection in wild type mice and in the G93A mouse model of amyotrophic lateral sclerosis.

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Satellite cell proliferation in low frequency-stimulated fast muscle of hypothyroid rat

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https://pubmed.ncbi.nlm.nih.gov/18467368

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Skeletal muscle properties in a transgenic mouse model for amyotrophic lateral sclerosis: effects of creatine treatment

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Identifiers

DOI

10.1113/JPHYSIOL.2007.149286

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18467368

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 January 2020

PubMed publication ID

18467368

1 reference

stated in

Europe PubMed Central

PubMed publication ID

18467368

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18467368%20AND%20SRC:MED&resulttype=core&format=json

retrieved

7 January 2020

 

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