Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Neurobiology of disease - 1 Aug 2003

Derave Wim, Van Den Bosch Ludo, Lemmens Griet, Eijnde Bert O, Robberecht Wim, Hespel Peter

Abstract excerpt

The present study was undertaken to identify the metabolic and contractile characteristics of fast- and slow-twitch skeletal muscles in a transgenic mouse model of amyotrophic lateral sclerosis (ALS). In addition, we investigated the effects of oral creatine supplementation on muscle functional c...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Creatine
Share to Glycogen
Share to Models, Animal

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Muscle Contraction

Share to Muscle Fibers, Fast-Twitch

Share to Muscle Fibers, Slow-Twitch

Share to Muscular Atrophy

Share to Superoxide Dismutase-1

Source

Identifiers

PMID: 12901841
DOI: 10.1016/s0969-9961(03)00041-x

Genes

SOD1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-12901841-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Skeletal muscle properties in a transgenic mouse model for amyotrophic lateral sclerosis: effects of creatine treatment.PMID 12901841Read ↗

Running and swimming prevent the deregulation of the BDNF/TrkB neurotrophic signalling at the neuromuscular junction in mice with amyotrophic lateral sclerosis.Semantic proximity Read ↗

Respiratory impairment in a mouse model of amyotrophic lateral sclerosis.Semantic proximity Read ↗

Creatine kinase knockout mice--what is the phenotype: skeletal muscle.Semantic proximity Read ↗

Metabolic Changes Associated With Muscle Expression of SOD1G93ASemantic proximity Read ↗

Caloric restriction transiently improves motor performance but hastens clinical onset of disease in the Cu/Zn-superoxide dismutase mutant G93A mouse.Semantic proximity Read ↗

Up-regulation of mitochondrial uncoupling protein 3 reveals an early muscular metabolic defect in amyotrophic lateral sclerosis.Semantic proximity Read ↗

Creatine-supplemented diet extends Purkinje cell survival in spinocerebellar ataxia type 1 transgenic mice but does not prevent the ataxic phenotype.Semantic proximity Read ↗

Interaction of chronic creatine depletion and muscle unloading: effects on postural locomotor muscles.Semantic proximity Read ↗

L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy.Semantic proximity Read ↗

Long-lived Ames dwarf mouse exhibits increased antioxidant defense in skeletal muscle.Semantic proximity Read ↗

Contingent intramuscular boosting of P2XR7 axis improves motor function in transgenic ALS mice.Semantic proximity Read ↗

Of mice and men: Reconciling preclinical ALS mouse studies and human clinical trialsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.