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| Title / Description | Infantile-onset Pompe disease: biceps |
| Accession | GSE4410 |
| Summary | Analysis of biceps biopsies from untreated patients with infantile-onset Pompe. Pompe disease is a genetic disorder resulting from lysosomal acid alpha-glucosidase (GAA) deficiency; the severest form affects infants. Results provide insight into the molecular basis of infantile-onset Pompe disease. |
| Organism | mouse |
| Platform | GPL339 |
| Normalized | False |
| Parsed SOFT file |
| Differential expression method | Characteristic Direction |
| Cutoff | 500 |
| Drug_name | SODIUM BUTYRATE |
| Smiles | CCCC(=O)[O-].[Na+] |
| Pubchem_cid | 5222465 |
| Cell_type | Colonic epithelial cells - 24 Hours |
| Organism | mouse |
| Principal Component Analysis | |
| Hierarchical clustering |
| Gene lists | Enrichr | L1000CDS2 | PAEA | Crowdsourcing | |
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