User contributions
From WikiPathways
(Latest | Earliest) View (newer 50) (older 50) (20 | 50 | 100 | 250 | 500)
- 14:48, 13 August 2018 Homo sapiens:Purine metabolism and related disorders (Changed last disease nodes to labels)
- 14:26, 13 August 2018 Homo sapiens:Purine metabolism and related disorders (Changed more disease nodes to labels)
- 14:11, 13 August 2018 Homo sapiens:Purine metabolism and related disorders (Changed first diseases into labels with URLs to OMIM)
- 14:04, 13 August 2018 Homo sapiens:Purine metabolism and related disorders (Changed interaction arrows from PRPP to AICARP, to connect proper with right part of PW)
- 13:25, 3 August 2018 DeSl
- 14:59, 2 August 2018 Homo sapiens:Mevalonate arm of cholesterol biosynthesis pathway with inhibitors (Added chembl compound prefix for IDs.)
- 13:48, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Changed location of THMEM126B)
- 11:42, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Modified description)
- 11:42, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Modified description)
- 11:37, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Modified description)
- 11:32, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Annotated MT-ND1 (really the last protein without annotation)
- 11:29, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Modified description)
- 11:27, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Annotated last protein node, added states to all chaperone nodes.)
- 11:20, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Ontology Term : 'oxidative phosphorylation pathway' added !)
- 11:16, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Added linkout to Electron transport chain PW.)
- 11:12, 31 July 2018 Homo sapiens:Electron transport chain: OXPHOS system in mitochondria (Added linkout to assemly PW for Complex 1)
- 11:10, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Modified description)
- 11:06, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Modified description)
- 11:05, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Modified description)
- 11:00, 31 July 2018 Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (Ontology Term : 'electron transport chain pathway' added !)
- 10:57, 31 July 2018 N Homo sapiens:Mitochondrial complex I assembly model OXPHOS system (New pathway)
- 12:37, 25 July 2018 WikiPathways Webservice/API (changed link to swagger.ui)
- 12:10, 25 July 2018 Homo sapiens:Degradation pathway of sphingolipids, including diseases (Changed part of wrong symbols in globoside example 2)
- 12:01, 25 July 2018 Homo sapiens:Degradation pathway of sphingolipids, including diseases (changed weird symbols (again))
- 11:12, 25 July 2018 Homo sapiens:Degradation pathway of sphingolipids, including diseases (Changed two IDs from Ensembl Human to Ensembl, changed disease nodes to labels with linkouts to OMIM.)
- 10:03, 25 July 2018 Homo sapiens:Degradation pathway of sphingolipids, including diseases (changed weird symbols)
- 10:03, 25 July 2018 Homo sapiens:Degradation pathway of sphingolipids, including diseases (changed weird symbols)
- 09:55, 25 July 2018 Homo sapiens:Degradation pathway of sphingolipids, including diseases (changed weird symbols)
- 09:52, 25 July 2018 Homo sapiens:Degradation pathway of sphingolipids, including diseases (Reverted to version '08:44, 23 May 2018' by <a href="/index.php/User:DeSl" title="User:DeSl">DeSl</a>)
- 08:58, 25 July 2018 Homo sapiens:Codeine and morphine metabolism (Added stereochemically correct ID for Norcodeine; changed layout slightly due to overlapping references on nodes.)
- 07:56, 25 July 2018 Homo sapiens:Codeine and morphine metabolism (Ontology Term : 'Gilbert syndrome' added !)
- 15:15, 24 July 2018 Homo sapiens:Electron transport chain: OXPHOS system in mitochondria (Removed licence number and last modified part.)
- 15:14, 24 July 2018 Homo sapiens:Electron transport chain: OXPHOS system in mitochondria (changed title slightly)
- 11:23, 20 July 2018 CLemmens (Discussion edited) (top)
- 11:23, 20 July 2018 N Pathway contributions to WikiPathways (1) (New page: Dear Claire Lemmens, Back in 2016, you created two pathway for WikiPathways, https://www.wikipathways.org/index.php/Pathway:WP3602 and https://www.wikipathways.org/index.php?title=Pathway...) (top)
- 11:11, 20 July 2018 Homo sapiens:Glycerophospholipid biosynthetic pathway (Ontology Term : 'glycerophospholipid metabolic pathway' added !)
- 13:18, 14 July 2018 WikiPathways
- 10:57, 5 July 2018 Homo sapiens:WikiPathways Test: Metabolites and Metabolic Interactions (Added new testcase for recently added LIPID Maps IDs to wikidata)
- 09:54, 5 July 2018 Homo sapiens:WikiPathways Test: Metabolites and Metabolic Interactions (Added correct ID for latest testcase.)
- 09:46, 5 July 2018 Homo sapiens:WikiPathways Test: Metabolites and Metabolic Interactions (Added lit. ref to BridgeDb paper and BridgeDb Cytoscape app paper.)
- 09:43, 5 July 2018 Homo sapiens:WikiPathways Test: Metabolites and Metabolic Interactions (Changed version number.)
- 09:41, 5 July 2018 Homo sapiens:WikiPathways Test: Metabolites and Metabolic Interactions (Added more testcases)
- 09:33, 4 July 2018 Homo sapiens:Rett syndrome (Changed Ref. layout)
- 09:25, 4 July 2018 Homo sapiens:Rett syndrome (Changed Ref. layout)
- 09:23, 4 July 2018 Homo sapiens:Rett syndrome (Changed Ref. layout)
- 09:06, 4 July 2018 Homo sapiens:Rett syndrome (Changes layout (again).)
- 09:05, 4 July 2018 Homo sapiens:Rett syndrome (More layout changes, every single line should be visible now in terms of connectivity)
- 09:02, 4 July 2018 Homo sapiens:Rett syndrome (Changed layout some more)
- 09:00, 4 July 2018 Homo sapiens:Rett syndrome (Changed layout, how lines are connected etc.)
- 08:52, 4 July 2018 Homo sapiens:Rett syndrome (Found Gene ID in left bottom corner, which screwed up visualisation)
(Latest | Earliest) View (newer 50) (older 50) (20 | 50 | 100 | 250 | 500)