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Morphological and functional alterations of neuromuscular synapses in a mouse model of ACTA1 congenital myopathy

Human Molecular Genetics(2023)10.1093/hmg/ddad183Source: DataRank Database

Morphological and functional alterations of neuromuscular synapses in a mouse model of ACTA1 congenital myopathy is a research paper published in Human Molecular Genetics (2023). On theSindex it has a DataRank of 0. It has been cited 5 times.

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0DataRank · unranked

Scored on demand from live citation data

Open Access5 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (6 grants)Impact (FWCI 0.46)OA: greenTopics (27)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 (2)

Weichun Lin ORCID,Yun Liu ORCID

Live enrichment

PubMed:37883471 PMC:PMC10800017 OpenAlex:https://openalex.org/W4387966806

The Paul D. Wellstone Muscular Dystrophy Cooperative Research Center

Grant: HD-087351

National Institute of Neurological Disorders and Strokes

Grant: R01 NS055028

NICHD NIH HHS

Grant: U54 HD087351

NICHD NIH HHS

Grant: P50 HD087351

NIH HHS

National Institutes of Health

FWCI

0.46

Citation Percentile

0.6%

Influential Citations

Citation Trend

2023

2025

2026

greenLicense: https://academic.oup.com/pages/standard-publication-reuse-rights

repositoryhttps://pmc.ncbi.nlm.nih.gov/articles/PMC10800017/pdf/ddad183.pdf

publisherhttps://academic.oup.com/hmg/advance-article-pdf/doi/10.1093/hmg/ddad183/53343979/ddad183.pdf

publisherhttps://academic.oup.com/hmg/article-pdf/33/3/233/56290047/ddad183.pdf

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/10800017

Fields of Study

Muscle Physiology and DisordersCardiomyopathy and Myosin StudiesIon channel regulation and functionMedicineBiology

MeSH Terms

ActinsAnimalsDisease Models, AnimalHumansMuscular DiseasesMutationMyotonia CongenitaNeuromuscular JunctionMyopathies, NemalineMuscle, SkeletalMice

Keywords

Nemaline myopathySkeletal muscleBiologyActinNeuroscienceAnatomyCell biologySynapseNeuromuscular junctionacetylcholine receptorSkeletal Muscle Α-actin

Sustainable Development Goals

SDG 0: Good health and well-being