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590
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ShareScore release 0.9.0
Dataset results
590 results for “muscular dystrophies.”
Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy [RNA-seq]
GEO Series GSE232047. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy.
GEO Series GSE232049. Mus musculus. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing.
Targeting Galectin-3 to modulate inflammation in LAMA2-deficient congenital muscular dystrophy
GEO Series GSE292894. Mus musculus. 18 samples. Type: Expression profiling by high throughput sequencing.
Gene expression profiles using microarrays in diaphragm of normal Beagle dogs and Beagle-based canine muscular dystrophy (CXMDJ) before and 1 hour after initial respiration.
GEO Series GSE32460. Canis lupus familiaris. 15 samples. Type: Expression profiling by array.
The microRNA, miR-133b, functions to slow Duchenne muscular dystrophy pathogenesis
GEO Series GSE156267. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
Cardiac response to thromboxane-prostanoid receptor antagonism in a mouse model of muscular dystrophy
GEO Series GSE120625. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy [snRNA-seq]
GEO Series GSE232048. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
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.
Hit-and-run silencing of endogenous DUX4 by targeting DNA hypomethylation on D4Z4 repeats in facioscapulohumeral muscular dystrophy [RNA-seq]
GEO Series GSE201178. Homo sapiens. 4 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>
Dataset related to the article "Reprogramming of dermal fibroblasts from a Duchenne muscular dystrophy patient carrying a deletion of exons 45–50 into an induced pluripotent stem cell line (CCMi005-A)"
<p>This record contains raw data related to the article " "Reprogramming of dermal fibroblasts from a Duchenne muscular dystrophy patient carrying a deletion of exons 45–50 into an induced pluripotent stem cell line (CCMi005-A)"</p> <p>Abstract</p> <p>Duchenne muscular dystrophy (DMD) is an X-linked syndrome that affects skeletal and cardiac muscle and is caused by mutation of the dystrophin gene. Induced pluripotent stem cells (iPSCs) were generated from dermal fibroblasts by electroporation with episomal vectors containing the reprogramming factors (OCT4, SOX2, LIN28, KLF4, and L-MYC). The donor carried an out-of-frame deletion of exons 45–50 of the dystrophin gene. The established iPSC line exhibited normal morphology, expressed pluripotency markers, had normal karyotype and possessed trilineage differentiation potential.</p>
The Expanded Access Use of Viltolarsen in Duchenne Muscular Dystrophy With Confirmed Exon 53 Amenable Mutation
ClinicalTrials.gov study NCT04337112. IPD Sharing: Not stated. Countries: 0. Publications: 0.
miR-206 modulates the pathogenesis of muscular dystrophy of mdx mice
GEO Series GSE36077. Mus musculus. 6 samples. Type: Expression profiling by array.
Cardiac Myoediting Mitigates Cardiomyopathy in Human and Mouse Models of Duchenne Muscular Dystrophy
GEO Series GSE169551. Mus musculus. 4 samples. Type: Expression profiling by high throughput sequencing.
Hit-and-run silencing of endogenous DUX4 by targeting DNA hypomethylation on D4Z4 repeats in facioscapulohumeral muscular dystrophy
GEO Series GSE201185. Homo sapiens. 11 samples. Type: Methylation profiling by genome tiling array; Expression profiling by high throughput sequencing.
Epigenetic control of myogenic identity of human muscle stem cells in Duchenne Muscular Dystrophy
GEO Series GSE232667. Homo sapiens. 18 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Gene expression data from Duchenne muscular dystrophy patients versus controls
GEO Series GSE38417. Homo sapiens. 22 samples. Type: Expression profiling by array.
Net39 protects muscle nuclei from mechanical stress during the pathogenesis of Emery-Dreifuss muscular dystrophy [ChIP-seq]
GEO Series GSE232046. Mus musculus. 4 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
ScienceDex guides
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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.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.