User contributions
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- 15:46, 5 February 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Update EEF2K interactions) (top)
- 15:24, 5 February 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Update with more EEF2K interactors)
- 15:25, 4 February 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Arrange EEF2K interactions)
- 15:09, 3 February 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Add interactions to EEF2K)
- 14:55, 3 February 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Update EEF2K interactions)
- 14:35, 3 February 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Add more interactions to EEF2K)
- 12:08, 3 February 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Update of interactions)
- 12:19, 30 January 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (Ontology Term : 'disease pathway' added !)
- 11:42, 30 January 2025 Homo sapiens:16p12.2 copy number variation syndrome (520kb) (add more interactions)
- 13:29, 22 January 2025 N Homo sapiens:16p12.2 copy number variation syndrome (520kb) (New pathway)
- 13:10, 13 December 2024 Alval (→About Me) (top)
- 11:44, 11 December 2024 Homo sapiens:16p13.11 copy number variation syndrome (Correct and add more interactions)
- 15:25, 10 December 2024 Homo sapiens:16p13.11 copy number variation syndrome (Correct and add interactions; Add proteins to the complexes)
- 08:02, 9 December 2024 N Homo sapiens:16p13.11 copy number variation syndrome (New pathway)
- 12:58, 28 November 2024 N Alval (Initial user page) (top)
- 12:58, 28 November 2024 N Alval (Initial user page)
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