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236 results for “Inflammatory Cytokines”

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geo12/100

Cystatin C modulates the release of inflammatory cytokines in Lipopolysaccharide-activated monocytes

GEO Series GSE61572. Homo sapiens. 16 samples. Type: Expression profiling by array.

openGEO-OpenSep 2017View details →
geo12/100

Expression analysis of inflammatory cytokines in exhaled breath condensates from pediatric patients with sickle cell disease, asthma, sickle cell disease and asthma, and controls

GEO Series GSE150056. Homo sapiens. 29 samples. Type: Protein profiling by protein array.

openGEO-OpenMay 2020View details →
geo12/100

Baseline Expression of Inflammatory Cytokines and Receptors in the HCC1806 Human Breast Cancer Cell Line

GEO Series GSE80642. Homo sapiens. 3 samples. Type: Expression profiling by RT-PCR.

openGEO-OpenMay 2016View details →
geo12/100

Baseline Expression of Inflammatory Cytokines and Receptors in the HCC1954 Human Breast Cancer Cell Line

GEO Series GSE80643. Homo sapiens. 3 samples. Type: Expression profiling by RT-PCR.

openGEO-OpenMay 2016View details →
geo12/100

Effect of IQGAP3 silencing on HaCaT keratinocytes under normal conditions or inflammatory cytokine stimulation

GEO Series GSE248548. Homo sapiens. 12 samples. Type: Expression profiling by high throughput sequencing.

openGEO-OpenApr 2024View details →
geo12/100

siRNA-mediated knockdown of Sp3 induces a pro-inflammatory pattern of cytokine production: relevance to MS

GEO Series GSE7102. Homo sapiens. 12 samples. Type: Expression profiling by array.

openGEO-OpenFeb 2008View details →
geo12/100

Baseline Expression of Inflammatory Cytokines and Receptors in the T47D Human Breast Cancer Cell Line

GEO Series GSE80647. Homo sapiens. 3 samples. Type: Expression profiling by RT-PCR.

openGEO-OpenMay 2016View details →
geo12/100

Baseline Expression of Inflammatory Cytokines and Receptors in the Normal Human Breast

GEO Series GSE80625. Homo sapiens. 3 samples. Type: Expression profiling by RT-PCR.

openGEO-OpenMay 2016View details →
geo12/100

Baseline Expression of Inflammatory Cytokines and Receptors in the MCF7 Human Breast Cancer Cell Line

GEO Series GSE80644. Homo sapiens. 3 samples. Type: Expression profiling by RT-PCR.

openGEO-OpenMay 2016View details →
geo12/100

Baseline Expression of Inflammatory Cytokines and Receptors in the ZR-75 Human Breast Cancer Cell Line

GEO Series GSE80648. Homo sapiens. 3 samples. Type: Expression profiling by RT-PCR.

openGEO-OpenMay 2016View details →
geo12/100

Baseline Expression of Inflammatory Cytokines and Receptors in Normal Breast Tissue and Seven Breast Cancer Cell Lines

GEO Series GSE80649. Homo sapiens. 24 samples. Type: Expression profiling by RT-PCR.

openGEO-OpenMay 2016View details →
geo12/100

Isosorbide fatty acid diesters have synergistic anti-inflammatory effects in cytokine-induced tissue culture models of atopic dermatitis

GEO Series GSE217468. Homo sapiens. 15 samples. Type: Expression profiling by array.

openGEO-OpenNov 2022View details →
geo12/100

Exogenous Interleukin-10 versus Glucocorticoids: Effect on Gene Expression and Pro-inflammatory Cytokine Release in Polymorphonuclear Leukocytes and Monocytes of the Newborn

GEO Series GSE35683. Homo sapiens. 30 samples. Type: Expression profiling by array.

openGEO-OpenFeb 2012View details →
zenodo12/100

Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques

<p>Mazzaccaro D, Dolci M, Perego F, Delbue S, Giannetta M, Cardani R, Valentina Renna L, Costa E, Corsi-Romanelli MM, Galli C, Pariani E, Nano G, Clemente C, Basilico N. Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques. Ann Vasc Surg. 2021 Dec 11:S0890-5096(21)00912-2. doi: 10.1016/j.avsg.2021.10.070. Epub ahead of print. PMID: 34902464.</p> <p>Abstract</p> <p><strong>Background:&nbsp;</strong>To investigate the presence of genetic material of viral agents and the serum level of inflammatory cytokines in patients submitted to carotid endarterectomy having vulnerable versus stable atherosclerotic plaques.</p> <p><strong>Methods:&nbsp;</strong>Data of patients consecutively submitted to carotid endarterectomy for a significant stenosis from July 2019 to December 2019 were prospectively collected. The genetic material of Epstein-Barr (EBV), CitoMegalo (CMV), Herpes Simplex (HSV), Varicella-Zoster (VZV) and Influenza (IV) Viruses was searched in the patient&#39;s plaques, both in the &quot;mid&quot; of the plaque and in an adjacent lateral portion of no-plaque area. The serum levels of TNF-&alpha;, IL-1&beta;, IL-6, IL10 and CCL5 were determined. The obtained results were then correlated to the histologic vulnerability of the removed carotid plaque. P values &lt; 0.05 were considered statistically significant.</p> <p><strong>Results:&nbsp;</strong>Data of 50 patients were analyzed. A vulnerable plaque was found in 31 patients (62%). The genome of CMV, HSV, VZV and IV was not found in any of the vascular samples, while the EBV genome was found in the &quot;mid&quot; of 2 vulnerable plaques, but not in their respective control area. Eighty-two percent of patients who did not receive anti-IV vaccination (23/28) had vulnerable carotid plaque, compared with 36% of vaccinated patients (8/22, P = 0.001). Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque (73.6 &plusmn; 238.2 vs. 3.9 &plusmn; 13.1 pg/ml, P= 0.01, and 45.9 &plusmn; 103.6 vs. 10.1 &plusmn; 25.3 pg/ml, P= 0.01, respectively), independent of comorbidities, viral exposure or flu vaccination.</p> <p><strong>Conclusions:&nbsp;</strong>The EBV genome was found in the &quot;core&quot; of 2 vulnerable carotid plaques, but not in their respective adjacent control. Influenza vaccination was associated with a lower incidence of carotid plaque vulnerability. Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque.</p>

restrictedFeb 2022View details →
zenodo12/100

Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques

<p>Mazzaccaro D, Dolci M, Perego F, Delbue S, Giannetta M, Cardani R, Valentina Renna L, Costa E, Corsi-Romanelli MM, Galli C, Pariani E, Nano G, Clemente C, Basilico N. Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques. Ann Vasc Surg. 2022 May;82:325-333. doi: 10.1016/j.avsg.2021.10.070. Epub 2021 Dec 11. PMID: 34902464.</p> <p>Abstract</p> <p><strong>Background:&nbsp;</strong>To investigate the presence of genetic material of viral agents and the serum level of inflammatory cytokines in patients submitted to carotid endarterectomy having vulnerable versus stable atherosclerotic plaques.</p> <p><strong>Methods:&nbsp;</strong>Data of patients consecutively submitted to carotid endarterectomy for a significant stenosis from July 2019 to December 2019 were prospectively collected. The genetic material of Epstein-Barr (EBV), CitoMegalo (CMV), Herpes Simplex (HSV), Varicella-Zoster (VZV) and Influenza (IV) Viruses was searched in the patient&#39;s plaques, both in the &quot;mid&quot; of the plaque and in an adjacent lateral portion of no-plaque area. The serum levels of TNF-&alpha;, IL-1&beta;, IL-6, IL10 and CCL5 were determined. The obtained results were then correlated to the histologic vulnerability of the removed carotid plaque. P values &lt; 0.05 were considered statistically significant.</p> <p><strong>Results:&nbsp;</strong>Data of 50 patients were analyzed. A vulnerable plaque was found in 31 patients (62%). The genome of CMV, HSV, VZV and IV was not found in any of the vascular samples, while the EBV genome was found in the &quot;mid&quot; of 2 vulnerable plaques, but not in their respective control area. Eighty-two percent of patients who did not receive anti-IV vaccination (23/28) had vulnerable carotid plaque, compared with 36% of vaccinated patients (8/22, P = 0.001). Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque (73.6 &plusmn; 238.2 vs. 3.9 &plusmn; 13.1 pg/ml, P= 0.01, and 45.9 &plusmn; 103.6 vs. 10.1 &plusmn; 25.3 pg/ml, P= 0.01, respectively), independent of comorbidities, viral exposure or flu vaccination.</p> <p><strong>Conclusions:&nbsp;</strong>The EBV genome was found in the &quot;core&quot; of 2 vulnerable carotid plaques, but not in their respective adjacent control. Influenza vaccination was associated with a lower incidence of carotid plaque vulnerability. Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque.</p>

restrictedJan 2023View details →
zenodo12/100

Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques

<p>Mazzaccaro D, Dolci M, Perego F, Delbue S, Giannetta M, Cardani R, Valentina Renna L, Costa E, Corsi-Romanelli MM, Galli C, Pariani E, Nano G, Clemente C, Basilico N. Viral Agents and Systemic Levels of Inflammatory Cytokines in Vulnerable and Stable Atherosclerotic Carotid Plaques. Ann Vasc Surg. 2022 May;82:325-333. doi: 10.1016/j.avsg.2021.10.070. Epub 2021 Dec 11. PMID: 34902464.</p> <p>Abstract</p> <p><strong>Background:&nbsp;</strong>To investigate the presence of genetic material of viral agents and the serum level of inflammatory cytokines in patients submitted to carotid endarterectomy having vulnerable versus stable atherosclerotic plaques.</p> <p><strong>Methods:&nbsp;</strong>Data of patients consecutively submitted to carotid endarterectomy for a significant stenosis from July 2019 to December 2019 were prospectively collected. The genetic material of Epstein-Barr (EBV), CitoMegalo (CMV), Herpes Simplex (HSV), Varicella-Zoster (VZV) and Influenza (IV) Viruses was searched in the patient&#39;s plaques, both in the &quot;mid&quot; of the plaque and in an adjacent lateral portion of no-plaque area. The serum levels of TNF-&alpha;, IL-1&beta;, IL-6, IL10 and CCL5 were determined. The obtained results were then correlated to the histologic vulnerability of the removed carotid plaque. P values &lt; 0.05 were considered statistically significant.</p> <p><strong>Results:&nbsp;</strong>Data of 50 patients were analyzed. A vulnerable plaque was found in 31 patients (62%). The genome of CMV, HSV, VZV and IV was not found in any of the vascular samples, while the EBV genome was found in the &quot;mid&quot; of 2 vulnerable plaques, but not in their respective control area. Eighty-two percent of patients who did not receive anti-IV vaccination (23/28) had vulnerable carotid plaque, compared with 36% of vaccinated patients (8/22, P = 0.001). Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque (73.6 &plusmn; 238.2 vs. 3.9 &plusmn; 13.1 pg/ml, P= 0.01, and 45.9 &plusmn; 103.6 vs. 10.1 &plusmn; 25.3 pg/ml, P= 0.01, respectively), independent of comorbidities, viral exposure or flu vaccination.</p> <p><strong>Conclusions:&nbsp;</strong>The EBV genome was found in the &quot;core&quot; of 2 vulnerable carotid plaques, but not in their respective adjacent control. Influenza vaccination was associated with a lower incidence of carotid plaque vulnerability. Serum levels of TNF-&alpha; and IL-6 were higher in patients with a vulnerable plaque compared to patients with a stable plaque.</p>

restrictedJan 2023View details →

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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.

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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.

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Last verified 2026-04-29Open record

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.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record