User contributions
From WikiPathways
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- 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) (top)
- 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 !)
- 05:58, 30 June 2020 Homo sapiens:MAPK pathway in congenital thyroid cancer (Ontology Term : 'altered Erk5 MAPK signaling pathway' added !)
- 05:57, 30 June 2020 Homo sapiens:MAPK pathway in congenital thyroid cancer (Ontology Term : 'Pathway Ontology' added !)
- 06:16, 29 June 2020 Homo sapiens:MAPK pathway in congenital thyroid cancer (Modified title)
- 07:15, 26 June 2020 Homo sapiens:GPR143 in melanocytes and retinal pigment epithelium cells (GPR143 change)
- 15:02, 25 June 2020 Homo sapiens:Overlap between signal transduction pathways contributing to LMNA laminopathies (corrected a few conversions and added states)
- 14:28, 25 June 2020 Homo sapiens:Amino acid conjugation of benzoic acid (removed wrong ID from Benzoic acid AMP ester - ID requested from Chebi)
- 14:01, 25 June 2020 Homo sapiens:Proximal tubule transport (changed MIM conversion to graphical line)
- 13:33, 25 June 2020 Homo sapiens:7q11.23 copy number variation syndrome (POM121)
- 07:29, 25 June 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 14:11, 24 June 2020 N Homo sapiens:15q13.3 copy number variation syndrome (New pathway)
- 14:09, 24 June 2020 Homo sapiens:7q11.23 copy number variation syndrome (Ontology Term : 'genetic disease' added !)
- 14:09, 24 June 2020 Homo sapiens:7q11.23 copy number variation syndrome (Ontology Term : 'Williams-Beuren syndrome' added !)
- 14:09, 24 June 2020 Homo sapiens:7q11.23 copy number variation syndrome (Ontology Term : 'disease pathway' added !)
- 13:52, 24 June 2020 Homo sapiens:7q11.23 copy number variation syndrome (Modified description)
- 13:51, 24 June 2020 Homo sapiens:7q11.23 copy number variation syndrome (Modified title)
- 13:46, 24 June 2020 Homo sapiens:15q11.2 copy number variation syndrome (Modified description)
- 13:08, 24 June 2020 RareDisease/SpecialIssue
- 10:50, 24 June 2020 RareDisease
- 09:02, 24 June 2020 RareDisease/FeaturedPathways
- 08:59, 24 June 2020 RareDisease/News
- 08:23, 24 June 2020 Homo sapiens:15q11.2 copy number variation syndrome (Ontology Term : 'genetic disease' added !)
- 08:22, 24 June 2020 Homo sapiens:15q11.2 copy number variation syndrome (Ontology Term : 'disease pathway' added !)
- 08:22, 24 June 2020 Homo sapiens:15q11.2 copy number variation syndrome (Ontology Term : 'chromosome 15q11.2 deletion syndrome' added !)
- 08:18, 24 June 2020 Homo sapiens:15q11.2 copy number variation syndrome (work in progress)
(Latest | Earliest) View (newer 50) (older 50) (20 | 50 | 100 | 250 | 500)
