Research ID
hum0139-v1Release info
Research title
Research for drug discovery and elucidation of pathophysiology using disease-specific iPS cells
Research overview
- Aims
- To address how status of KRAS in iPS cells impacts upon self-renewal and differentiation propensity
- Methods
- Roles of KRAS on stemness were investigated in the context of induced pluripotent stem cells (iPSCs). KRAS mutant (G13C/WT) and wild-type isogenic (WT/WT) iPSCs from a Ras-associated autoimmune leukoproliferative disorder (RALD) patient were used. Retention of self-renewal and capacity for neuronal differentiation were compared.
- Participants/materials
- A RALD patient-derived iPSC clones (one with KRAS G13C mutation and the other one with no mutation derived from the same patient).
- URL
- N/A
Datasets
| Cart | Dataset ID | Type of data | Analysis method | Access criteria | Date published |
|---|---|---|---|---|---|
| JGAD000205 | NGS (Exome) |
| Controlled-access (Type I) | 2020-09-28 |
Data provider
- Principal investigator
- Makoto Otsu
- Affiliation
- Institute of Medical Science, University of Tokyo
Research projects
| Name | URL |
|---|---|
The program for intractable diseases research utilizing disease-specific iPS cells | N/A |
Grants
| Name | Title | Project number |
|---|---|---|
Research Center Network for Realization of Regenerative Medicine, Japan Agency for Medical Research and Development (AMED) | The program for intractable diseases research utilizing disease-specific iPS cells |
|
Related publications
| Title | DOI | Dataset ID |
|---|---|---|
Status of KRAS in iPS cells impacts upon self-renewal and differentiation propensity. |
Controlled access users
No use of the controlled access data has been recorded.