User contributions

From WikiPathways

Search for contributions

 Show contributions of new accounts only
 IP Address or username: Namespace: all (Main) Talk User User talk WikiPathways WikiPathways talk Image Image talk MediaWiki MediaWiki talk Template Template talk Help Help talk Category Category talk Thread Thread talk Summary Summary talk Pw Old Pw Old Talk Pathway Pathway Talk Wishlist Wishlist Talk Portal Portal Talk

From year (and earlier): From month (and earlier): all January February March April May June July August September October November December

(Latest | Earliest) View (newer 50) (older 50) (20 | 50 | 100 | 250 | 500)

• 12:49, 29 March 2023 Homo sapiens:1p36 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 12:46, 29 March 2023 Homo sapiens:8p23.1 copy number variation syndrome‎ (Modified title)
• 12:32, 29 March 2023 Homo sapiens:Kleefstra syndrome‎ (added missing ID)
• 12:29, 29 March 2023 Homo sapiens:Kleefstra syndrome‎ (Ontology Term : 'altered histone modification pathway' added !)
• 12:29, 29 March 2023 Homo sapiens:Kleefstra syndrome‎ (Ontology Term : 'Kleefstra syndrome 2' added !)
• 12:28, 29 March 2023 Homo sapiens:Kleefstra syndrome‎ (Ontology Term : 'Kleefstra syndrome 1' added !)
• 12:28, 29 March 2023 Homo sapiens:Kleefstra syndrome‎ (Ontology Term : 'Kleefstra syndrome' added !)
• 12:28, 29 March 2023 Homo sapiens:Kleefstra syndrome‎ (Ontology Term : 'disease pathway' added !)
• 12:26, 29 March 2023 N Homo sapiens:Kleefstra syndrome‎ (New pathway)
• 09:02, 23 March 2023 Homo sapiens:Glycolysis and gluconeogenesis‎ (Replaced double-headed arrows with single arrows)
• 13:00, 7 March 2023 Homo sapiens:16p11.2 proximal deletion syndrome‎ (removed pseudogenes)
• 16:10, 8 November 2022 Homo sapiens:17q12 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 13:13, 29 September 2022 Mus musculus:Biogenic amine synthesis‎ (Changed identifier for D-Glutamic acid to L-Glutamic acid) (top)
• 05:59, 31 August 2022 Homo sapiens:Angiopoietin-like protein 8 regulatory pathway‎ (removed one "type your comment here")
• 09:44, 30 August 2022 Homo sapiens:Dravet syndrome‎ (Added release of GABA)
• 09:37, 30 August 2022 Homo sapiens:Dravet syndrome‎ (Ontology Term : 'GABAergic interneuron' added !)
• 12:53, 4 August 2022 Homo sapiens:Arsenic metabolism and reactive oxygen species generation‎ (Ontology Term : 'cancer' added !)
• 10:35, 3 August 2022 Homo sapiens:Dravet syndrome‎ (Modified description)
• 12:21, 27 July 2022 Homo sapiens:Dravet syndrome‎ (added more nodes)
• 08:12, 27 July 2022 Homo sapiens:Dravet syndrome‎ (Updated references)
• 07:18, 27 July 2022 Homo sapiens:Dravet syndrome‎ (Changed some faulty identifiers)
• 12:01, 15 July 2022 Homo sapiens:Prader-Willi and Angelman syndrome‎ (update in progress)
• 10:51, 15 July 2022 Homo sapiens:Prader-Willi and Angelman syndrome‎ (update)
• 11:08, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎ (Modified description)
• 10:44, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎
• 10:41, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎
• 10:32, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎ (Ontology Term : 'disease pathway' added !)
• 10:30, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎ (Ontology Term : 'portal hypertension' added !)
• 10:30, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎ (Ontology Term : 'chronic granulomatous disease' added !)
• 10:29, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎ (Ontology Term : 'Adams-Oliver syndrome' added !)
• 10:29, 13 July 2022 Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎ (Ontology Term : 'X-linked agammaglobulinemia' added !)
• 10:22, 13 July 2022 N Homo sapiens:Genetic causes of porto-sinusoidal vascular disease‎ (New pathway)
• 10:25, 24 June 2022 Homo sapiens:Estradiol regulation in porto-sinusoidal vascular disease‎ (Ontology Term : 'disease pathway' added !)
• 10:25, 24 June 2022 Homo sapiens:Estradiol regulation in porto-sinusoidal vascular disease‎ (Ontology Term : 'portal hypertension' added !)
• 10:24, 24 June 2022 Homo sapiens:Cholestasis‎ (Ontology Term : 'hepatocyte' added !)
• 12:08, 31 May 2022 Homo sapiens:Bardet-Biedl syndrome‎ (Ontology Term : 'ciliopathy' added !)
• 12:07, 31 May 2022 Homo sapiens:Bardet-Biedl syndrome‎ (Ontology Term : 'disease pathway' added !)
• 15:19, 20 May 2022 Homo sapiens:Markers of kidney cell lineage‎ (work in progress)
• 14:23, 20 May 2022 Homo sapiens:Markers of kidney cell lineage‎ (Modified title)
• 14:17, 20 May 2022 Homo sapiens:Markers of kidney cell lineage‎
• 12:03, 20 May 2022 N Homo sapiens:Markers of kidney cell lineage‎ (New pathway)
• 11:48, 22 April 2022 RareDisease/SpecialIssue‎ (top)
• 10:56, 22 April 2022 Homo sapiens:2q37 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 10:56, 22 April 2022 Homo sapiens:2q21.1 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 10:55, 22 April 2022 Homo sapiens:2q11.2 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 10:54, 22 April 2022 Homo sapiens:Creatine pathway‎ (Updated pathway node layout)
• 10:53, 22 April 2022 Homo sapiens:Leukotriene metabolic pathway‎ (Updated layout for pathways)
• 10:49, 22 April 2022 Homo sapiens:Gamma-glutamyl cycle for the biosynthesis and degradation of glutathione, including diseases‎ (Adapted layout for pathways)
• 12:37, 20 April 2022 Homo sapiens:2q13 copy number variation syndrome‎ (Ontology Term : 'disease pathway' added !)
• 08:18, 6 April 2022 RareDisease/SpecialIssue‎

(Latest | Earliest) View (newer 50) (older 50) (20 | 50 | 100 | 250 | 500)