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590
datasets available to search
ShareScore release 0.9.0
Dataset results
590 results for “muscular dystrophies.”
fhl2b expression ameliorates muscular dystrophy
GEO Series GSE242137. Danio rerio. 40 samples. Type: Expression profiling by high throughput sequencing.
Prednisolone rescues Duchenne Muscular Dystrophy phenotypes in human pluripotent stem cells-derived skeletal muscle in vitro
GEO Series GSE164874. Homo sapiens. 45 samples. Type: Expression profiling by high throughput sequencing.
Yin Yang 1 Deficiency in Skeletal Muscle Stem Cell Aggravates Muscle Fibrosis in Duchenne Muscular Dystrophy Mouse by Disrupting Muscle Stem Cell/Macrophage/Fibro-adipogenic Progenitor Crosstalk [Hi-C
GEO Series GSE250193. Mus musculus. 6 samples. Type: Other.
In vivo genome editing restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers [Nanopore sequencing]
GEO Series GSE167584. Homo sapiens. 12 samples. Type: Other.
Expression profiling in the muscular dystrophies
GEO Series GSE465. Homo sapiens. 57 samples. Type: Expression profiling by array.
In vivo genome editing restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers [Amplicon-seq]
GEO Series GSE167572. Homo sapiens. 60 samples. Type: Other.
Mouse Models for Muscular Dystrophy
GEO Series GSE2112. Mus musculus. 26 samples. Type: Expression profiling by array.
Transcriptional profiling in facioscapulohumeral muscular dystrophy to identify candidate biomarkers
GEO Series GSE36398. Homo sapiens. 50 samples. Type: Expression profiling by array.
DNA Replication Timing is Maintained Genome-wide in Primary Human Myoblasts Independent of D4Z4 Contraction in FSH Muscular Dystrophy
GEO Series GSE34197. Homo sapiens. 7 samples. Type: Genome variation profiling by genome tiling array.
Transcriptional profile in dermal fibroblasts from patients with collagen VI related muscular dystrophy
GEO Series GSE103270. Homo sapiens. 19 samples. Type: Expression profiling by high throughput sequencing.
Effects of chronic hypoxia on Duchenne Muscular Dystrophy Drosophila melanogaster model
GEO Series GSE15879. Drosophila melanogaster. 16 samples. Type: Expression profiling by array.
Transcriptome analysis of collagen VI-related muscular dystrophy muscle biopsies [Microarray].
GEO Series GSE103972. Homo sapiens. 36 samples. Type: Expression profiling by array.
Asynchronous remodeling is a driver of failed regeneration in Duchenne muscular dystrophy
GEO Series GSE109178. Homo sapiens. 49 samples. Type: Expression profiling by array.
Deletion of DMD exon 52 in the pig results in fulminant muscular dystrophy
GEO Series GSE44096. Sus scrofa. 13 samples. Type: Expression profiling by array.
Rbfox1 downregulation and altered Calpain 3 splicing by FRG1 in a mouse model of facioscapulohumeral muscular dystrophy (FSHD).
GEO Series GSE32073. Mus musculus. 24 samples. Type: Expression profiling by array.
Human iPSC-based model for Duchenne muscular dystrophy
GEO Series GSE70955. Homo sapiens. 15 samples. Type: Expression profiling by array.
Metabolic reprogramming of skeletal muscle by resident macrophages points to CSF1R inhibitors as muscular dystrophy therapeutics (RNA-Seq).
GEO Series GSE198054. Mus musculus. 20 samples. Type: Expression profiling by high throughput sequencing.
Dataset related to the article "Complete phenotype rescue through the restoration of full-length dystrophin using CRISPR/Cas9 genome editing in Duchenne muscular dystrophy patient-derived iPSCs carrying the deletion of two exons."
<p><span>This record contains raw data related to the article Dataset related to the article “Complete phenotype rescue through the restoration of full-length dystrophin using CRISPR/Cas9 genome editing in Duchenne muscular dystrophy patient-derived iPSCs carrying the deletion of two exons".</span></p> <p><span>Here we describe for the first time the restoration of the full-length dystrophin protein, by CRISPR/Cas9, in an iPSC derived from a Duchenne patient carrying the deletion of two exons, allowing the recovery of the cardiac pathological phenotypes and mechanisms, as assessed from the transcriptional, structural, and functional point of view.</span></p>
A Study of Deflazacort (Emflaza®) in Participants With Duchenne Muscular Dystrophy (DMD)
ClinicalTrials.gov study NCT03642145. IPD Sharing: Not stated. Countries: 0. Publications: 0.
A Multicenter Randomized Placebo-Controlled Double-Blind Study to Assess Efficacy and Safety of Glutamine and Creatine Monohydrate in Duchenne Muscular Dystrophy (DMD)
ClinicalTrials.gov study NCT00018109. IPD Sharing: Not stated. Countries: 1. Publications: 0.
ScienceDex guides
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These curated guides explain access requirements, typical timelines, costs, and reuse considerations for widely used research datasets.
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.