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225
datasets available to search
ShareScore release 0.9.0
Dataset results
225 results for “Dilated Cardiomyopathy”
A leiomodin 2 neonatal dilated cardiomyopathy causing mutation results inaltered actin-regulatory gene signatures andcardiomyocyte dysfunction
GEO Series GSE271871. Homo sapiens; Mus musculus. 42 samples. Type: Expression profiling by high throughput sequencing.
Targeting MRTF/SRF in CAP2-dependent dilated cardiomyopathy delays disease onset
GEO Series GSE125603. Mus musculus. 16 samples. Type: Expression profiling by high throughput sequencing.
Cardiac-specific deletion of voltage dependent anion channel 2 leads to dilated cardiomyopathy by altering calcium homeostasis
GEO Series GSE168487. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
Deleterious assembly of the lamin A/C mutant p.S143P causes ER stress in familial dilated cardiomyopathy
GEO Series GSE82290. Homo sapiens. 11 samples. Type: Expression profiling by array.
Distinct cardiac transcriptomic clustering in titin and lamin a/c-associated dilated cardiomyopathy patients
GEO Series GSE146621. Homo sapiens. 29 samples. Type: Expression profiling by high throughput sequencing.
Deletion of the RS domain in RBM20 leads to dilated cardiomyopathy
GEO Series GSE212799. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Identification of signature genes of Dilated cardiomyopathy Using Integrated bioinformatics analysis
GEO Series GSE224211. Mus musculus. 6 samples. Type: Expression profiling by high throughput sequencing.
Methylome analysis reveals alterations in DNA methylation in the regulatory regions of left ventricle development genes in human dilated cardiomyopathy (methylation)
GEO Series GSE81337. Homo sapiens. 27 samples. Type: Methylation profiling by array.
TEAD1 trapping by the Q353R-Lamin A/C causes dilated cardiomyopathy.
GEO Series GSE190977. Mus musculus; Homo sapiens. 30 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Isogenic human pluripotent stem cell disease models reveal actin binding Rho activating protein deficiency underlies the cardiac troponin T DK210 mutation-induced familial dilated cardiomyopathy II
GEO Series GSE154097. Homo sapiens. 30 samples. Type: Expression profiling by high throughput sequencing.
Partial restoration of the mitochondrial dysfunction by AAV-Ant1 (Slc25a4) transduction protects against dilated cardiomyopathy in Slc25a4-/- plus mtDNA mutant mice
GEO Series GSE280991. Mus musculus. 115 samples. Type: Expression profiling by high throughput sequencing.
KDM8 epigenetically controls cardiac metabolism to prevent initiation of dilated cardiomyopathy
GEO Series GSE215794. Homo sapiens; Mus musculus. 37 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Cardiac Fibrosis in Dilated Cardiomyopathy: Transcriptomics Insights, Histological Correlations, and Organoid Model Verifications
GEO Series GSE246299. Homo sapiens. 67 samples. Type: Expression profiling by high throughput sequencing.
Simtuzumab attenuates Loxl2-mediated extracellular matrix remodeling and preserves cardiac function in LMNA mutation-induced dilated cardiomyopathy
GEO Series GSE312730. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Unravelling the etiology of dilated cardiomyopathy through differential miRNA-mRNA interactome
GEO Series GSE243406. Homo sapiens. 15 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.
Depletion of m6A reader protein YTHDC1 induces dilated cardiomyopathy by abnormal splicing of Titin
GEO Series GSE164353. Mus musculus. 18 samples. Type: Expression profiling by high throughput sequencing; Other.
Dilated cardiomyopathy vs Myocarditis
GEO Series GSE120567. Homo sapiens. 16 samples. Type: Expression profiling by high throughput sequencing.
Serum Circulating Proteins from Pediatric Dilated Cardiomyopathy Patients Cause Pathologic Remodeling and Cardiomyocyte Stiffness
GEO Series GSE181051. Homo sapiens; Rattus norvegicus. 62 samples. Type: Expression profiling by high throughput sequencing; Expression profiling by RT-PCR; Protein profiling by protein array.
Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes is Associated with Differential Gene Expression and DNA Methylation in Human Dilated Cardiomyopathy [RNA-Seq]
GEO Series GSE120836. Homo sapiens. 10 samples. Type: Expression profiling by high throughput sequencing.
I536T variant of RBM20 affects splicing of cardiac structural proteins that are causative for developing dilated cardiomyopathy
GEO Series GSE201018. Mus musculus. 3 samples. Type: Expression profiling by high throughput sequencing.
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.