MSC_busulfan_small_intestine_organoids
This dataset represent the RNA-seq, which was done on untreated small intestinal organoids; small intestinal organoids treated with chemotherapeutic, busulfan; untreated small intestinal organoids co-cultured wth mesenchymak stromal/stem cells (MSCs; busulfan treated small intestinal organoids co-cultured with MSCs. The same set of samples was done for 3 different primary bone marrow MSC donors.
- 12 samples
- DAC: EGAC00001000432
- Technology: NextSeq 500
- DS DUO:0000007 (version: 2021-02-23)disease specific researchThis data use permission indicates that use is allowed provided it is related to the specified disease.ModifiersMONDO:0004335
- NPUNCU DUO:0000018 (version: 2021-02-23)not for profit, non commercial use onlyThis data use modifier indicates that use of the data is limited to not-for-profit organizations and not-for-profit use, non-commercial use.
- PUB DUO:0000019 (version: 2021-02-23)publication requiredThis data use modifier indicates that requestor agrees to make results of studies using the data available to the larger scientific community.
- COL DUO:0000020 (version: 2021-02-23)collaboration requiredThis data use modifier indicates that the requestor must agree to collaboration with the primary study investigator(s).
Access policy for study "Regenerative effects of MSC treatment on busulfan-induced small intestine damaged organoids.'
* DUO:0000007; MONDO:0004335 (only for purposes that are related to the specific disease, namely regarding the digestive tract) * DUO:0000018 (only by not-for-profit organizations) * DUO:0000019 (only if the requestor agrees to make the results, of the studies using these data, available to the larger scientific community.) * DUO:0000020 (only if the requestor agrees to collaborate with the primary study investigator(s)). For details contact dacdbg@umcutrecht.nl
Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.
| Study ID | Study Title | Study Type |
|---|---|---|
| Other |