User contributions
From WikiPathways
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- 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 !)
- 15:34, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Ontology Term : 'chromosome 16p11.2 deletion syndrome, 220kb' added !)
- 15:34, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Ontology Term : 'disease pathway' added !)
- 15:34, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Ontology Term : 'genetic disease' added !)
- 15:33, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Modified description)
- 15:32, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Modified description)
- 15:28, 27 July 2020 N Homo sapiens:16p11.2 distal deletion syndrome (New pathway)
- 15:20, 27 July 2020 N Homo sapiens:16p11.2 proximal deletion syndrome (New pathway)
- 15:54, 23 July 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 15:16, 23 July 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 11:18, 22 July 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 11:04, 22 July 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 13:47, 16 July 2020 RareDisease/FeaturedPathways
- 13:45, 16 July 2020 RareDisease/News
- 13:43, 16 July 2020 Homo sapiens:Nitric oxide metabolism in cystic fibrosis (fixed unconnected line)
- 13:09, 16 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (SPDYE11)
- 12:40, 16 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (update on TRIM50)
- 13:43, 9 July 2020 Homo sapiens:Nitric oxide metabolism in cystic fibrosis (Modified description)
- 13:42, 9 July 2020 Homo sapiens:Nitric oxide metabolism in cystic fibrosis (Ontology Term : 'disease pathway' added !)
- 13:41, 9 July 2020 Homo sapiens:Nitric oxide metabolism in cystic fibrosis (Ontology Term : 'cystic fibrosis' added !)
- 13:41, 9 July 2020 Homo sapiens:Nitric oxide metabolism in cystic fibrosis (Ontology Term : 'nitric oxide mediated signaling pathway' added !)
- 13:39, 9 July 2020 N Homo sapiens:Nitric oxide metabolism in cystic fibrosis (New pathway)
- 07:16, 7 July 2020 Homo sapiens:15q11.2 copy number variation syndrome (FRX pathway)
- 04:43, 2 July 2020 Homo sapiens:Amino acid conjugation of benzoic acid (added new ChEBI ID for Benzoic acid AMP ester)
- 14:19, 30 June 2020 Homo sapiens:7q11.23 copy number variation syndrome
- 05:59, 30 June 2020 Homo sapiens:MAPK pathway in congenital thyroid cancer (Ontology Term : 'thyroid cancer' added !)
- 05:58, 30 June 2020 Homo sapiens:MAPK pathway in congenital thyroid cancer (Ontology Term : 'thyroid cancer pathway' added !)
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