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ShareScore release 0.9.0
Dataset results
80 results for “Spinocerebellar ataxia”
Dual targeting of brain region-specific kinases potentiates neurological rescue in Spinocerebellar ataxia type 1
GEO Series GSE151276. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Gain of function of the ATXN1-CIC complex drives cerebellar pathology in Spinocerebellar ataxia type 1
GEO Series GSE108256. Mus musculus. 22 samples. Type: Expression profiling by high throughput sequencing.
Identifying common and region-specific disease signatures in Spinocerebellar Ataxia type 1 cortex and cerebellum
GEO Series GSE211678. Mus musculus. 12 samples. Type: Expression profiling by high throughput sequencing.
Gain of function of the ATXN1-CIC complex drives cerebellar pathology in Spinocerebellar ataxia type 1 (part 1)
GEO Series GSE108254. Mus musculus. 7 samples. Type: Expression profiling by high throughput sequencing.
Modeling spinocerebellar ataxias 2 and 3 with iPSCs reveals a major role of glutamate in disease pathology
GEO Series GSE96826. Homo sapiens. 11 samples. Type: Expression profiling by array.
Epigenetic and transcriptional impairments in a retina of SCA7140Q/140Q and SCA7140Q/5Q knock-in mouse model of spinocerebellar ataxia type 7
GEO Series GSE181325. Mus musculus. 19 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1
GEO Series GSE218302. Mus musculus. 104 samples. Type: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing.
Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1 [RNA-seq]
GEO Series GSE218283. Mus musculus. 59 samples. Type: Expression profiling by high throughput sequencing.
Epigenetic and transcriptional impairments in a retina of SCA7140Q/140Q and SCA7140Q/5Q knock-in mouse model of spinocerebellar ataxia type 7 [ChIP-seq]
GEO Series GSE181324. Mus musculus. 12 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Glucocorticoid receptor-dependent therapeutic efficacy of tauroursodeoxycholic acid in preclinical models of Spinocerebellar ataxia type 3
GEO Series GSE252250. Mus musculus. 9 samples. Type: Expression profiling by high throughput sequencing.
RNA sequencing of a Spinocerebellar ataxia type 3 (SCA3) mouse model containing the full human ATXN3 gene with a repeat expansion of 75-80 CAGs I
GEO Series GSE107958. Mus musculus. 53 samples. Type: Expression profiling by high throughput sequencing.
Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1 [CUT&RUN]
GEO Series GSE218301. Mus musculus. 45 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Use of a New Smartphone Application to Determine Changes in Eyeblink Conditioning From Home Training in Individuals With Spinocerebellar Ataxia
ClinicalTrials.gov study NCT06177626. IPD Sharing: NO. Countries: 1. Publications: 0.
Stemchymal® for Polyglutamine Spinocerebellar Ataxia
ClinicalTrials.gov study NCT06397274. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Umbilical Cord Mesenchymal Stem Cells Therapy (19#iSCLife®-SA) for Patients With Spinocerebellar Ataxia
ClinicalTrials.gov study NCT03378414. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Efficacy of Cerebellar Transcranial Magnetic Stimulation to Treat Hereditary Spinocerebellar Ataxias
ClinicalTrials.gov study NCT06898645. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Transcriptomic profiling of peripheral blood mononuclear cells (PBMC) from patients with Parkinson’s disease (PD), Spinocerebellar ataxia (SCA2) and control subjects
GEO Series GSE75249. Homo sapiens. 33 samples. Type: Expression profiling by array.
Dateset related to article "Spinocerebellar Ataxia Type 1: One‑Year Longitudinal Study to Identify Clinical and MRI Measures of Disease Progression in Patients and Presymptomatic Carriers "
<p>This dataset contains clinical information (neuropsychological evaluations, structural MRI measures, etc.) on patients with Spinocerebellar Ataxia included in the study reported at title</p>
Expanded Access Protocol of Troriluzole in Patients With Spinocerebellar Ataxia (SCA)
ClinicalTrials.gov study NCT06034886. IPD Sharing: Not stated. Countries: 0. Publications: 0.
Transcriptome analysis of Spinocerebellar Ataxia 17 Aug
GEO Series GSE72176. Mus musculus. 8 samples. Type: Expression profiling by array.
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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.