User contributions
From WikiPathways
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- 13:15, 9 October 2020 Homo sapiens:Glucocorticoid receptor pathway
- 13:14, 9 October 2020 Homo sapiens:Glucocorticoid receptor pathway
- 13:02, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 12:14, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 11:34, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 11:05, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 10:16, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 15:03, 8 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 14:07, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (first draft finished)
- 13:38, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 12:52, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 12:35, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 16:22, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 15:24, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 12:42, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 11:54, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 09:34, 1 October 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 09:22, 1 October 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 08:54, 25 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 08:05, 25 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 15:52, 21 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 15:41, 21 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 08:36, 18 September 2020 RareDisease/FeaturedPathways (→Copy number variation syndromes)
- 08:35, 18 September 2020 RareDisease/News
- 14:37, 17 September 2020 Homo sapiens:7q11.23 copy number variation syndrome (Modified description)
- 14:36, 17 September 2020 Homo sapiens:7q11.23 copy number variation syndrome (Modified title)
- 14:35, 17 September 2020 Homo sapiens:22q11.2 copy number variation syndrome (Modified title)
- 12:43, 25 August 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 11:56, 25 August 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 11:16, 25 August 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 07:11, 21 August 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 07:03, 21 August 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 13:58, 20 August 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 13:14, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Modified description)
- 13:05, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Ontology Term : 'disease pathway' added !)
- 13:04, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Ontology Term : 'chromosome 15q13.3 microdeletion syndrome' added !)
- 13:03, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Ontology Term : 'genetic disease' added !)
- 13:00, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 09:06, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 12:19, 19 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 08:59, 28 July 2020 RareDisease/FeaturedPathways
- 08:56, 28 July 2020 RareDisease/News
- 08:21, 28 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 08:10, 28 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 06:28, 28 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 16:20, 27 July 2020 Homo sapiens:22q11.2 copy number variation syndrome (Undergoing reconstruction and completion of deleted gene list)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Modified description)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Ontology Term : 'genetic disease' added !)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Ontology Term : 'disease pathway' added !)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Ontology Term : 'chromosome 16p11.2 deletion syndrome, 220kb' added !)
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