Find research datasets worth reusing
Search datasets from major research repositories and use ShareScore to quickly assess how well each record supports discovery, access, and reuse.
54
datasets available to search
ShareScore release 0.9.0
Dataset results
54 results for “Dystrophin”
CRISPR/Cas9 editing of directly reprogrammed myogenic progenitors restores dystrophin expression in a dystrophic mouse model
GEO Series GSE164599. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
In vivo genome editing restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers [RNA-seq]
GEO Series GSE167585. Homo sapiens. 18 samples. Type: Expression profiling by high throughput sequencing.
In vivo genome editing restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers [GUIDE-seq]
GEO Series GSE167583. Homo sapiens. 14 samples. Type: Other.
Signaling through the dystrophin glycoprotein complex affects the stress-dependent transcriptome in Drosophila
GEO Series GSE223505. Drosophila melanogaster. 15 samples. Type: Expression profiling by high throughput sequencing.
Dystrophin deficiency dysregulates cell junctions during somite formation from pluripotent stem cells
GEO Series GSE233682. Homo sapiens. 41 samples. Type: Expression profiling by high throughput sequencing.
RNA sequencing of control and dystrophin-mutant engineered heart tissues from human induced pluripotent stem cell-derived cardiomyocytes
GEO Series GSE199242. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.
Safety and Dystrophin Expression of SPOT-mRNA03 in Duchenne Muscular Dystrophy (DMD) Patients
ClinicalTrials.gov study NCT07188012. IPD Sharing: NO. Countries: 1. Publications: 0.
Transcriptome of mouse primary muscle cultures upon dystrophin knockdown by RNAi.
GEO Series GSE20548. Mus musculus. 18 samples. Type: Expression profiling by array.
In vivo genome editing restores dystrophin expression in Duchenne muscular dystrophy patient muscle fibers [WES]
GEO Series GSE167586. Homo sapiens. 14 samples. Type: Other.
Multi-level omics analysis of gene expression in a murine model of dystrophin loss and therapeutic restoration [mRNA]
GEO Series GSE64418. Mus musculus. 11 samples. Type: Expression profiling by array.
Multi-level omics analysis of dystrophin loss and therapeutic restoration in a murine model [microRNA]
GEO Series GSE64419. synthetic construct; Mus musculus. 11 samples. Type: Non-coding RNA profiling by array.
Array profiling of dystrophin-deficient mice with a secondary glycosylation defect
GEO Series GSE16438. Mus musculus. 24 samples. Type: Expression profiling by array.
Dystrophin-deficient and dystrophin and utrophin double-deficient mice crossed with mice with full-length hDMD genes
GEO Series GSE6790. Mus musculus. 9 samples. Type: Expression profiling by array.
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.
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.
Molecular profiles (HG-U95A) of dystrophin-deficient and normal human muscle
GEO Series GSE1004. Homo sapiens. 24 samples. Type: Expression profiling by array.
Molecular profiles of dystrophin-deficient and normal murine muscle
GEO Series GSE897. Mus musculus. 36 samples. Type: Expression profiling by array.
Molecular profiles(HG-U95B,C,D,E) of dystrophin-deficient and normal human skeletal muscle
GEO Series GSE1007. Homo sapiens. 86 samples. Type: Expression profiling by array.
RNA sequencing of TA skeletal muscle of mice with conditional ablation of dystrophin within the myofiber
GEO Series GSE284723. Mus musculus. 9 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>
ScienceDex guides
Understand access before you commit
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.