User contributions
From WikiPathways
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- 13:36, 28 May 2021 Homo sapiens:Serine metabolism (adapted disease node graphics to the one in the legend)
- 10:46, 28 May 2021 RareDisease/News
- 10:45, 28 May 2021 RareDisease/FeaturedPathways
- 10:44, 28 May 2021 RareDisease/FeaturedPathways
- 10:14, 28 May 2021 RareDisease/News
- 09:44, 28 May 2021 RareDisease/FeaturedPathways
- 09:41, 28 May 2021 RareDisease/FeaturedPathways
- 09:37, 28 May 2021 RareDisease/News
- 09:29, 28 May 2021 RareDisease/SpecialIssue
- 09:26, 28 May 2021 RareDisease/FeaturedPathways
- 09:19, 28 May 2021 RareDisease/FeaturedPathways (→Inborn errors of metabolism)
- 09:15, 28 May 2021 RareDisease/News
- 15:17, 27 May 2021 Caenorhabditis elegans:Fatty acid beta-oxidation 2 (added metabolite identifiers)
- 15:07, 27 May 2021 Caenorhabditis elegans:Fatty acid beta-oxidation 2 (added anchors and catalysis)
- 15:02, 27 May 2021 Caenorhabditis elegans:Fatty acid beta-oxidation 3 (added catalysis, anchors and metabolite identifiers)
- 14:54, 27 May 2021 Caenorhabditis elegans:Fatty acid biosynthesis (connected line, added metabolite identifiers and proper catalysis and anchors)
- 14:39, 27 May 2021 Caenorhabditis elegans:Glycogen metabolism (replaced metabolite labels with metabolite nodes, connected lines) (top)
- 14:25, 27 May 2021 Caenorhabditis elegans:mRNA processing (converted graphical lines)
- 14:20, 27 May 2021 Caenorhabditis elegans:mRNA processing (converted graphical lines)
- 14:14, 27 May 2021 Caenorhabditis elegans:Translation factors (fixed unconnected line)
- 12:44, 29 April 2021 Homo sapiens:Neuroinflammation and glutamatergic signaling (Ontology Term : 'signaling pathway pertinent to the brain and nervous system' added !)
- 14:56, 15 April 2021 Homo sapiens:22q11.2 copy number variation syndrome (added literature reference)
- 11:19, 22 March 2021 RareDisease (top)
- 11:18, 22 March 2021 RareDisease/SpecialIssue
- 16:10, 18 March 2021 Homo sapiens:FOXP3 in COVID-19 (graphical adjustments)
- 16:02, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (Modified title)
- 16:01, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (Ontology Term : 'severe acute respiratory syndrome' added !)
- 16:01, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (Ontology Term : 'disease pathway' added !)
- 16:00, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (small graphical adaptions)
- 15:10, 18 March 2021 Homo sapiens:SARS-CoV-2 and COVID-19 pathway (added S2 identifiers)
- 14:53, 18 March 2021 Homo sapiens:SARS-CoV-2 innate immunity evasion and cell-specific immune response (fixed unconnected lines, added S1 ID)
- 14:43, 18 March 2021 Homo sapiens:Mitochondrial immune response to SARS-CoV-2 (Updated S1/S2 identifiers)
- 14:32, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (added IDs for S1 and S2)
- 08:37, 12 March 2021 Homo sapiens:15q13.3 copy number variation syndrome (update in progress)
- 08:32, 12 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (fixed unconnected line)
- 08:29, 12 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (update in progress)
- 08:09, 12 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (update in progress)
- 07:45, 12 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (graphical update)
- 16:19, 11 March 2021 Homo sapiens:16p11.2 distal deletion syndrome (update in progress)
- 16:08, 11 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 15:48, 11 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 15:46, 11 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (updated to GRCH37)
- 15:26, 11 March 2021 Homo sapiens:16p11.2 distal deletion syndrome (Modified description)
- 15:24, 11 March 2021 Homo sapiens:16p11.2 distal deletion syndrome (update to GHRCh37)
- 15:17, 11 March 2021 Homo sapiens:16p11.2 proximal deletion syndrome (Modified description)
- 14:01, 11 March 2021 Homo sapiens:15q13.3 copy number variation syndrome (Modified description)
- 14:00, 11 March 2021 Homo sapiens:15q13.3 copy number variation syndrome (update to GHRC37)
- 13:44, 11 March 2021 Homo sapiens:15q11.2 copy number variation syndrome (Modified description)
- 13:43, 11 March 2021 Homo sapiens:15q11.2 copy number variation syndrome (updated to GRCh37)
- 13:39, 11 March 2021 Homo sapiens:3q29 copy number variation syndrome (update to GRCh37)
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