ID
45412
Beschrijving
Principal Investigator: Geoffrey Ginsburg, MD, PhD, Institute for Genome Science and Policy, Duke University, Durham, NC, USA MeSH: https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000548 The study protocol for both cohorts has been previously described (Journal of Thrombosis and Thrombolysis 2012:1-12). HV1 cohort: Briefly 50 healthy volunteers were exposed to two weeks of 325mg/day aspirin after which whole blood RNA was collected in PAXgene tubes and profiled by microarray before and after aspirin exposure. The pre-aspirin samples were profiled on the U133A 2.0 array and the post-aspirin samples were profiled on the U1333plus 2.0 array. HV2 cohort: Briefly 53 healthy volunteers were exposed to four weeks of 325mg/day aspirin after which whole blood RNA was collected in PAXgene tubes and profiled by U133plus 2.0 array before and after aspirin exposure.
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Trefwoorden
Versies (1)
- 20-11-22 20-11-22 - Chiara Middel
Houder van rechten
Geoffrey Ginsburg, MD, PhD, Institute for Genome Science and Policy, Duke University, Durham, NC, USA
Geüploaded op
20 november 2022
DOI
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Licentie
Creative Commons BY 4.0
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dbGaP phs000548 Aspirin Pharmacogenomics
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID and consent group of healthy participants involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Subject ID, sample ID, and sample use variable obtained from the healthy participants involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Subject ID, platelet function score, pre vs. post aspirin time point obtained from healthy participants [HV1] involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Subject ID, platelet function score, pre vs. post aspirin time point obtained from healthy participants [HV2] involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Sample ID, body site where sample was collected, and analyte type of samples obtained from healthy participants involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
Similar models
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- Subject ID and consent group of healthy participants involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Subject ID, sample ID, and sample use variable obtained from the healthy participants involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Subject ID, platelet function score, pre vs. post aspirin time point obtained from healthy participants [HV1] involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Subject ID, platelet function score, pre vs. post aspirin time point obtained from healthy participants [HV2] involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
- Sample ID, body site where sample was collected, and analyte type of samples obtained from healthy participants involved in the "Phase I Clinical Trial Describing the Pharmacogenomics of Aspirin" project.
C0680251 (UMLS CUI [1,2])
C1552738 (UMLS CUI [1,2])
C0332152 (UMLS CUI [1,3])