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28
datasets available to search
ShareScore release 0.9.0
Dataset results
28 results for “Becker Muscular Dystrophy”
L-citrulline and Metformin in Becker's Muscular Dystrophy
ClinicalTrials.gov study NCT02018731. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Phase 2 Study of EDG-5506 in Becker Muscular Dystrophy (GRAND CANYON)
ClinicalTrials.gov study NCT05291091. IPD Sharing: NO. Countries: 12. Publications: 0.
Effectiveness of 5-week Digital Respiratory Practice in Children With Duchenne and Becker Muscular Dystrophies.
ClinicalTrials.gov study NCT06363526. IPD Sharing: NO. Countries: 1. Publications: 0.
CRD007 for the Treatment of Duchenne Muscular Dystrophy, Becker Muscular Dystrophy and Symptomatic Carriers
ClinicalTrials.gov study NCT01540604. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Transcriptomic Profile of Skeletal Muscle Biopsies from Duchenne and Becker Muscular Dystrophy Patients
GEO Series GSE291383. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
Intron Mutations and Early Transcription Termination in Duchenne and Becker muscular dystrophy
GEO Series GSE175861. Homo sapiens. 11 samples. Type: Expression profiling by high throughput sequencing.
Dataset related to the article:"Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C."
<p>This record contains raw data related to the article: "Generation of the Becker muscular dystrophy patient derived induced pluripotent stem cell line carrying the DMD splicing mutation c.1705-8 T>C."</p> <p>Abstract:</p> <p>Becker Muscular dystrophy (BMD) is an X-linked syndrome characterized by progressive muscle weakness. BMD is generally less severe than Duchenne Muscular<br> Dystrophy. BMD is caused by mutations in the dystrophin gene that normally give rise to the production of a truncated but partially functional dystrophin protein. We<br> generated an induced pluripotent cell line from dermal fibroblasts of a BMD patient carrying a splice mutation in the dystrophin gene (c.1705-8 T>C). The iPSC cellline<br> displayed the characteristic pluripotent-like morphology, expressed pluripotency markers, differentiated into cells of the three germ layers and had a normal<br> karyotype.</p>
Dataset related to article "Quantitative Muscle MRI Protocol as Possible Biomarker in Becker Muscular Dystrophy"
<p>The database contains descriptive tables with clinical scores and quantitative MRI parameters values extracted from the thigh and the calf of the subjects involve in the study. A comparison table with the statistical correlation is also reported.</p>
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
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DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.