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Sucla2 Knock‐Out in Skeletal Muscle Yields Mouse Model of Mitochondrial Myopathy With Muscle Type–Specific Phenotypes

Journal of Cachexia Sarcopenia and Muscle(2024)10.1002/jcsm.13617Source: DataRank Database

Sucla2 Knock‐Out in Skeletal Muscle Yields Mouse Model of Mitochondrial Myopathy With Muscle Type–Specific Phenotypes is a research paper published in Journal of Cachexia Sarcopenia and Muscle (2024). On theSindex it has a DataRank of 0. It has been cited 4 times.

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Open Access4 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (7 grants)Impact (FWCI 0.76)OA: goldTopics (59)IDs (PubMed, PMC, OpenAlex)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (12)

Paul S. Hafen ORCID,Andrew Law,Catalina Matias,Timothy Meyer ORCID,Kathryn D. Fischer

Live enrichment

PubMed:39482887 PMC:PMC11634519 OpenAlex:https://openalex.org/W4403989457

National Institutes of Health

Grant: NIH R01AR070200

National Institutes of Health

Grant: R01GM098387

National Institutes of Health

Grant: R01NS126597

NIAMS NIH HHS

Grant: R01 AR070200

National Institutes of Health

Grant: 4R01GM098387-05

Succinyl-COA Synthetase Deficiency: A Model to Study Mitochondrial DNA (MTDNA) De

National Institutes of Health

Grant: 5R01AR070200-05

CELLULAR ENERGETICS AS A REGULATOR OF MUSCLE MASS AND MITOCHONDRIAL CONTENT DURING MUSCLE ATROPHY

National Institutes of Health

Grant: 5R01NS126597-04

Determination of pathogenetic mechanisms in cortex-specific Sucla2 deficiency as a model for mitochondrial encephalopathy

FWCI

0.76

Citation Percentile

0.7%

Citation Trend

2025

2026

goldLicense: cc-by

journalhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/jcsm.13617

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/jcsm.13617

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/jcsm.13617

journalhttps://doi.org/10.1002/jcsm.13617

repositoryhttps://pubmed.ncbi.nlm.nih.gov/39482887

Fields of Study

Genetic Neurodegenerative DiseasesMitochondrial Function and PathologyMuscle Physiology and Disorders03 medical and health sciences0303 health sciencesAnimalsMiceDisease Models, AnimalMuscle, SkeletalMice, KnockoutPhenotypeMitochondrial MyopathiesSuccinate-CoA LigasesHumans

MeSH Terms

AnimalsDisease Models, AnimalHumansPhenotypeSuccinate-CoA LigasesMitochondrial MyopathiesMice, KnockoutMuscle, SkeletalMice

Keywords

Skeletal muscleSarcopeniaMyopathyIn vivoWild typePhenotypeMolecular biologyBiologyInternal medicineEndocrinologyMutantMedicineBiochemistryGeneticsGeneExtensor digitorum longuscontractilitysoleusMitochondrial MyopathyFibre‐type SwitchingSuccinyl‐coa Synthetase570610Diseases of the musculoskeletal systemMiceSuccinate-CoA LigasesAnimalsHumansMuscle, SkeletalMice, KnockoutQM1-695Mitochondrial MyopathiesDisease Models, AnimalRC925-935Human anatomyOriginal Article

Sustainable Development Goals

SDG 0: Decent work and economic growth