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2,107
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ShareScore release 0.9.0
Dataset results
2,107 results for “Spectrum”
VG1 JUP PWS RESAMPLED SPECTRUM ANALYZER 48SEC V1.1
Voyager 1 Plasma Wave Subsystem (PWS) averaged spectrum analyzer 48.0 second data at Jupiter.
CRISPR-Cas9 base editor screening identifies the spectrum of MEN1 mutations impacting menin inhibitors in clinical trials [RNA-Seq]
GEO Series GSE294623. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
Gene expression profiles of fibroblasts and induced pluripotent stem cells (iPSCs) from individuals with Zellweger spectrum disorder (ZSD), a class of peroxisome biogenesis disorder, and healthy contr
GEO Series GSE43996. Homo sapiens. 35 samples. Type: Expression profiling by array.
B7-H3-Targeted CAR-Vδ1T Cells Exhibit Potent Broad-Spectrum Activity Against Solid Tumors
GEO Series GSE275242. Homo sapiens. 2 samples. Type: Expression profiling by high throughput sequencing.
SINE-MIR enhancer rewiring by Esrrb architecturally reprogram the pluripotency spectrum [HiChIP]
GEO Series GSE215452. Mus musculus. 6 samples. Type: Genome binding/occupancy profiling by high throughput sequencing; Other.
Dectin-1 intracellular domain determines species-specific ligand spectrum by modulating receptor sensitivity [mouse]
GEO Series GSE98825. Mus musculus. 2 samples. Type: Expression profiling by array.
SINE-MIR enhancer rewiring by Esrrb architecturally reprogram the pluripotency spectrum [Hi-C]
GEO Series GSE215449. Mus musculus. 8 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Using RNA sequencing to identify a putative network in placenta accreta spectrum
GEO Series GSE211003. Homo sapiens. 20 samples. Type: Expression profiling by high throughput sequencing; Non-coding RNA profiling by high throughput sequencing.
De novo structural variants in autism spectrum disorder disrupt distal regulatory interactions of neuronal genes [Hi-C]
GEO Series GSE281283. Homo sapiens. 6 samples. Type: Other.
Epigenome analysis of autism spectrum disorder samples
GEO Series GSE164563. Homo sapiens. 66 samples. Type: Methylation profiling by genome tiling array.
SINE-MIR enhancer rewiring by Esrrb architecturally reprogram the pluripotency spectrum [ChIP-Seq]
GEO Series GSE215207. Mus musculus. 17 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Vascular tumor spectrum in aP2-Cre mice
GEO Series GSE191239. Mus musculus. 8 samples. Type: Expression profiling by array.
CRISPR-Cas9 base editor screening identifies the spectrum of MEN1 mutations impacting menin inhibitors in clinical trials [CRISPRseq]
GEO Series GSE294624. Homo sapiens. 42 samples. Type: Other.
Dectin-1 intracellular domain determines species-specific ligand spectrum by modulating receptor sensitivity
GEO Series GSE98826. Mus musculus; Homo sapiens. 4 samples. Type: Expression profiling by array.
Gene Expresion in Ausitm Spectrum Disorders (ASD)
GEO Series GSE49105. Homo sapiens. 50 samples. Type: Expression profiling by array.
The novel RNA polymerase I transcription inhibitor PMR-116 exploits a critical therapeutic vulnerability in a broad-spectrum of high MYC malignancies [ChIP-Seq]
GEO Series GSE302076. Homo sapiens. 45 samples. Type: Genome binding/occupancy profiling by high throughput sequencing.
Dataset related to article "Profiling the Spectrum of Headache Disorders on 440 Breast Cancer Patients: Highlights on Clinical and Pathological Mechanisms"
<p>This record contains raw data related to article "Profiling the Spectrum of Headache Disorders on 440 Breast Cancer Patients: Highlights on Clinical and Pathological Mechanisms"</p><p>Abstract</p><p>Although widely studied, the association between migraines (M) and breast cancer (BC) risk remains evasive. In this prospective single-center study, 440 early or locally advanced BC patients were enrolled at IRCCS Humanitas Research Hospital. Clinical and demographical data were collected. Those who suffered from headaches were evaluated with the International Classification of Headache Disorders. M was found to be significantly more prevalent in BC patients: 56.1% versus an expected prevalence of 17% in the global population. M patients showed a higher risk of having stage II or III BC than stage I, which was more frequently found in the non-headache population. Interestingly, the frequency of headache attacks was positively correlated with estrogen (<i>r</i> = 0.11, <i>p</i> = 0.05) and progesterone (<i>r</i> = 0.15, <i>p</i> = 0.007) expression, especially in patients with migraine without aura. The higher the expression of hormone receptors in BC, the higher the headache frequency. Moreover, patients suffering from headaches showed an overall earlier onset of BC. Our findings challenge the idea of a net preventive role of M on BC, suggesting a rather complex interaction in which M mostly influences some BC subtypes and vice versa. Further multi-center studies with extended follow-up are needed.</p>
Broadband CP-FTMW spectrum of glycoaldehyde and water
Open the record for dataset details and reuse information.
SUFU haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum
<p>Joubert syndrome (JS) is a recessively inherited ciliopathy characterized by congenital ocular motor apraxia (COMA), developmental delay, intellectual disability, ataxia, multiorgan involvement and a unique cerebellar and brainstem malformation. Over 40 JS-associated genes are known, with diagnostic yield of 60-75%.</p> <p>In 2018, we reported homozygous hypomorphic missense variants of the SUFU gene in two families with mild JS. Recently, heterozygous truncating SUFU variants were identified in families with dominantly inherited COMA, occasionally associated with mild DD and subtle cerebellar anomalies.</p> <p>We reanalyzed NGS data in two cohorts comprising 1097 probands referred for genetic testing of JS genes. Heterozygous truncating and splice-site SUFU variants were detected in 22 patients from 17 families (1.5%) with strong male prevalence (86%), and in eight asymptomatic parents. The majority of affected children presented with the same constellation of neurological features seen at the mildest end of the JS spectrum, characterized by early onset hypotonia persisting in infancy, COMA, mild motor and speech delay and mild truncal and limb ataxia.</p> <p>Ataxia occurred in over 60% of the patients, while only about one third eventually manifested intellectual disability. Abnormal neonatal breathing was reported only in a minority of patients. Of note, macrocephaly was present in 19 out of 22 children, while extra-neurological involvement was extremely rare. Attention-Deficit/Hyperactivity Disorder, autism traits, obsessive-compulsive disrdr and other behavioral defects were reported in a minority of patient.</p>
Functional and structural impairment of small nerve fibers in patients suffering from hypermobile Ehlers Danlos Syndrome/Hypermobility Spectrum Disorder
<p>In this retrospective chart extraction from 79 hEDS/HSD patients referred to a pain center due to neuropathic pain or dysautonomia, both functional (Quantitative Sensory Testing (QST), N=79) and structural (IENFD, N=69) evaluations of small nerve fibers were analyzed in combination with clinical data and standardized questionnaires.</p>
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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.