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| Title / Description | Expression data from young and old healthy humans, as well as HGPS patients |
| Accession | GSE69391 |
| Summary | HGPS is a rare premature ageing disease, caused by a mutation in the LMNA gene, which activates a cryptic splice site, resulting in the production of a mutant lamin A isoform, called progerin. Sporadic usage of the same cryptic splice site has been observed with normal physiological aging. As it is unknown how HGPS causes premature ageing defects, we set out to determine the gene signature of both young healthy individuals, old healthy individuals, as well as HGPS patients. |
| Organism | Homo sapiens |
| Platform | GPL570 |
| Normalized | False |
| Parsed SOFT file |
| Differential expression method | Characteristic Direction |
| Cutoff | 500 |
| Cell | Blood |
| Perturbation | Aging |
| Disease | Aging |
| Young | 2 |
| Old | 18 |
| Time unit | months |
| Gene lists | Enrichr | L1000CDS2 | PAEA | |
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