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518
datasets available to search
ShareScore release 0.9.0
Dataset results
518 results for “Hereditary”
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss
GEO Series GSE64088. Homo sapiens. 308 samples. Type: Genome variation profiling by genome tiling array.
Hereditary Chronic Pancreatitis Induced Plasticity Cooperates with Mutant Kras in Early Pancreatic Carcinogenesis
GEO Series GSE297058. Mus musculus. 128 samples. Type: Expression profiling by high throughput sequencing; Other.
Human transthyretin (TTR) gene expression is markedly increased in repair phenotype of hereditary ATTR Schwann cell model
GEO Series GSE213537. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
Induced Endothelial Cell Cycle Arrest Prevents Arterio-venous Malformations in Hereditary Hemorrhagic Telangiectasia (Bulk RNA-Seq)
GEO Series GSE245197. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
MIRnome Profiling of Hereditary Pheochromocytoma and Paraganglioma Reveals Specific Signatures According to Primary Mutation: Possible Implications in the Differentiation Status of Tumor Cells
GEO Series GSE29742. Homo sapiens. 54 samples. Type: Non-coding RNA profiling by array.
Brca1 haploinsufficiency promotes early tumor onset and epigenetic alterations in a mouse model of hereditary breast cancer (scRNA-Seq)
GEO Series GSE247451. Mus musculus. 21 samples. Type: Expression profiling by high throughput sequencing.
Identification of Exosomal microRNA signature by liquid biopsy in Hereditary Hemorrhagic Telangiectasia patients
GEO Series GSE179382. Homo sapiens. 33 samples. Type: Non-coding RNA profiling by high throughput sequencing.
RNA Biological Characteristics at the Peak of Cell Death in Different Hereditary Retinal Degeneration Mutants
GEO Series GSE178928. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.
Mutations in RABL3 Alter KRAS Prenylation and are Associated with Hereditary Pancreatic Cancer
GEO Series GSE129081. Danio rerio. 7 samples. Type: Expression profiling by high throughput sequencing.
Application of RNA-seq for single nucleotide variation identification patients with hereditary diseases: analysis of trasncriptomic data and perspective use
GEO Series GSE273325. Homo sapiens. 54 samples. Type: Expression profiling by high throughput sequencing.
RNA-Seq and microarray analysis of the Xenopus inner ear transcriptome discloses orthologous OMIM® genes for hereditary disorders of hearing and balance
GEO Series GSE69701. Xenopus laevis. 1 samples. Type: Expression profiling by high throughput sequencing.
The pathogenesis of common Gjb2 mutation associated with human hereditary deafness in mice
GEO Series GSE215106. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
A human hereditary cardiomyopathy shares a genetic substrate with bicuspid aortic valve
GEO Series GSE185395. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Establishment of human Leber’s hereditary optic neuropathy model using iPSC-derived retinal organoids
GEO Series GSE305550. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
mRNA Levels in the Rat Liver Display Strain-Specific, Hereditary and AHR-Dependent Components
GEO Series GSE10448. Rattus norvegicus. 20 samples. Type: Expression profiling by array.
Distinct tumorigenic pathways within hereditary nonpolyposis colorectal cancer
GEO Series GSE36335. Homo sapiens. 132 samples. Type: Expression profiling by array.
Digitoxin Inhibits Epithelial-to-Mesenchymal-Transition in Hereditary Castration Resistant Prostate Cancer
GEO Series GSE133696. Rattus norvegicus. 6 samples. Type: Expression profiling by high throughput sequencing.
Single cell lineage tracing of pulmonary endothelial cells in mouse model of Hereditary Hemorrhagic Telangiectasia 2
GEO Series GSE269174. Mus musculus. 2 samples. Type: Expression profiling by high throughput sequencing.
dateset relate to article (submitted) Evaluation of mitochondrial dysfunction and idebenone responsiveness in fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) subjects.
<p>raw data related to the article at title</p>
Involvement of Monocytic B1 and B2 Receptors in Inflammation and Chronic Vascular Disease in Patients With Hereditary Bradykinetic Angioedema
ClinicalTrials.gov study NCT04032002. IPD Sharing: NO. 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.