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518
datasets available to search
ShareScore release 0.9.0
Dataset results
518 results for “Hereditary”
Expression profiling of peripheral blood gene expression of women with hereditary breast cancer and controls (set 1)
GEO Series GSE47860. Homo sapiens. 160 samples. Type: Expression profiling by array.
An antioxidant response phenotype is shared between hereditary and sporadic type 2 papillary renal cell carcinoma
GEO Series GSE26574. Homo sapiens. 67 samples. Type: Expression profiling by array.
microRNA expression profiles of reticulocytes for hereditary persistence of fetal hemoglobin and β-thalssemia minor with high fetal hemoglobin.
GEO Series GSE93973. Mus musculus; Rattus norvegicus; Homo sapiens. 14 samples. Type: Non-coding RNA profiling by array.
Activation of γ-globin gene expression by GATA1 and NF-Y in hereditary persistence of fetal hemoglobin
GEO Series GSE152338. Homo sapiens. 45 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Other.
Expression data from primary and hereditary pheochromocytomas (PHEOs) and paragangliomas (PGLs)
GEO Series GSE50442. Homo sapiens. 15 samples. Type: Expression profiling by array.
Expression profiling of peripheral blood gene expression of women with hereditary breast cancer and controls (set 2)
GEO Series GSE47861. Homo sapiens. 161 samples. Type: Expression profiling by array.
CRISPR/Cas9-mediated gene correction in newborn rabbits with hereditary tyrosinemia type I
GEO Series GSE142722. Oryctolagus cuniculus. 60 samples. Type: Genome variation profiling by high throughput sequencing.
Gene expression profiles of hiPSC-derived retinal ganglion cells in MT-ND4 mutated Leber's hereditary optic neuropathy
GEO Series GSE103619. Homo sapiens. 3 samples. Type: Expression profiling by array.
CRISPR/Cas9-mediated gene correction in newborn rabbits with hereditary tyrosinemia type I [DeepSeq1]
GEO Series GSE142704. Oryctolagus cuniculus. 18 samples. Type: Genome variation profiling by high throughput sequencing.
Modeling Hereditary Diffuse Leukoencephalopathy with Axonal Spheroids using microglia-sufficient brain organoids
GEO Series GSE271810. Homo sapiens. 32 samples. Type: Expression profiling by high throughput sequencing.
RNA-seq analysis of CRISPR/Cas9 generated human BMPR2 deficient endothelial cell lines harboring mutations characteristic for hereditary pulmonary hypertension (HPAH)
GEO Series GSE135312. Homo sapiens. 9 samples. Type: Expression profiling by high throughput sequencing.
GDF 15 in Sickle Cell Disease and Hereditary Spherocytosis
ClinicalTrials.gov study NCT01201135. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Efficacy of Topical Gentamycin for Hereditary Hypotrichosis Simplex Caused by Nonsense Mutations in CDSN
ClinicalTrials.gov study NCT03492866. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Phase III Randomized, Placebo-Controlled, Crossover Study of Soy Protein Isolate for Hereditary Hemorrhagic Telangiectasia
ClinicalTrials.gov study NCT00004654. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Pazopanib for the Treatment of Epistaxis in Hereditary Hemorrhagic Telangiectasia
ClinicalTrials.gov study NCT03850730. IPD Sharing: UNDECIDED. Countries: 0. Publications: 0.
EUROPAC-2 - Pain Treatment of Hereditary and Idiopathic Pancreatitis
ClinicalTrials.gov study NCT00142233. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Emergency Administration of EPI-743 to a Single Patient With Leber's Hereditary Optic Neuropathy [LHON]
ClinicalTrials.gov study NCT02300753. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Study of Heparin Prophylaxis of Hereditary Angioedema Exacerbations
ClinicalTrials.gov study NCT00004694. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Ranibizumab for the Management of Recurrent Nosebleeds in Patients With Hereditary Hemorrhagic Telangiectasia (HHT)
ClinicalTrials.gov study NCT01406639. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Study to Evaluate Ecallantide in Paediatric Patients With Acute Attacks of Hereditary Angioedema
ClinicalTrials.gov study NCT01253382. IPD Sharing: Not stated. Countries: 0. 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.