User contributions
From WikiPathways
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- 15:58, 26 July 2023 Homo sapiens:2q37 copy number variation syndrome (Modified description) (top)
- 15:56, 26 July 2023 Homo sapiens:2q37 copy number variation syndrome (Added information on chromosomal location found in the Kirov et al. 2014 paper)
- 15:48, 26 July 2023 Homo sapiens:2q21.1 copy number variation syndrome (Modified description) (top)
- 15:47, 26 July 2023 Homo sapiens:2q21.1 copy number variation syndrome (corrected legend position)
- 15:46, 26 July 2023 Homo sapiens:2q21.1 copy number variation syndrome (correcting starting positions according to Kirov et al 2014 in addition to Gimelli et al.)
- 15:18, 26 July 2023 Homo sapiens:NPHP1 deletion syndrome (Ontology Term : 'disease pathway' added !) (top)
- 15:18, 26 July 2023 Homo sapiens:NPHP1 deletion syndrome (Ontology Term : 'nephronophthisis 3' added !)
- 15:16, 26 July 2023 N Homo sapiens:NPHP1 deletion syndrome (New pathway)
- 14:44, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (Update to GRCh37 numbers) (top)
- 14:38, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (Reverted to version '12:56, 7 May 2022' by <a href="/index.php/User:Fehrhart" title="User:Fehrhart">Fehrhart</a>)
- 11:00, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (correction of chr numbers)
- 10:48, 26 July 2023 Homo sapiens:2q11.2 copy number variation syndrome (update to GRCh37)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'paranoid schizophrenia' added !) (top)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'autism spectrum disorder' added !)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'schizophrenia pathway' added !)
- 10:14, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Ontology Term : 'disease pathway' added !)
- 10:13, 26 July 2023 Homo sapiens:NRXN1 deletion syndrome (Modified description)
- 10:12, 26 July 2023 N Homo sapiens:NRXN1 deletion syndrome (New pathway)
- 09:38, 26 July 2023 Homo sapiens:TAR syndrome (Ontology Term : 'Disease' added !) (top)
- 09:38, 26 July 2023 Homo sapiens:TAR syndrome (Ontology Term : 'disease pathway' added !)
- 09:37, 26 July 2023 Homo sapiens:TAR syndrome (Modified description)
- 09:30, 26 July 2023 Homo sapiens:TAR syndrome (corrections and updates (done))
- 07:47, 26 July 2023 Homo sapiens:TAR syndrome (update in progress)
- 06:54, 26 July 2023 Homo sapiens:TAR syndrome (update in progress)
- 13:11, 24 July 2023 Homo sapiens:TAR syndrome (update)
- 12:36, 24 July 2023 Homo sapiens:TAR syndrome (upgrade)
- 12:00, 24 July 2023 Homo sapiens:TAR syndrome (upgrade)
- 10:08, 24 July 2023 Homo sapiens:1p36 copy number variation syndrome (Modified description)
- 10:06, 24 July 2023 Homo sapiens:1p36 copy number variation syndrome (update and corrections)
- 07:16, 11 July 2023 Homo sapiens:Primary ovarian insufficiency (Graphical update)
- 13:17, 5 June 2023 Homo sapiens:NF1 copy number variation syndrome (Ontology Term : 'disease pathway' added !)
- 13:17, 5 June 2023 Homo sapiens:NF1 copy number variation syndrome (Ontology Term : 'neurofibromatosis 1' added !)
- 09:04, 30 May 2023 Homo sapiens:1p36 copy number variation syndrome (Converted interaction to graphical line)
- 08:59, 30 May 2023 Homo sapiens:1p36 copy number variation syndrome (graphical update)
- 08:38, 30 May 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (Graphical update)
- 11:40, 4 May 2023 RareDisease/News (top)
- 15:21, 6 April 2023 Homo sapiens:1p36 copy number variation syndrome (Modified title)
- 15:19, 6 April 2023 Homo sapiens:11p11.2 copy number variation syndrome (Ontology Term : 'disease pathway' added !)
- 15:18, 6 April 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (Ontology Term : 'disease pathway' added !)
- 15:17, 6 April 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (Modified title)
- 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) (top)
- 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) (top)
- 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
- 08:10, 6 April 2022 Homo sapiens:Cholesterol synthesis disorders (Modified title)
- 08:09, 6 April 2022 Homo sapiens:Alstrom syndrome (connected unconnected lines)
- 08:07, 6 April 2022 Homo sapiens:Alstrom syndrome (Ontology Term : 'disease pathway' added !)
- 08:06, 6 April 2022 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis (Ontology Term : 'disease pathway' added !)
- 12:59, 28 March 2022 Homo sapiens:Dravet syndrome (Corrected references)
- 12:16, 28 March 2022 Homo sapiens:Dravet syndrome (Ontology Term : 'neuron' added !)
- 12:16, 28 March 2022 Homo sapiens:Dravet syndrome (Ontology Term : 'disease pathway' added !)
- 12:16, 28 March 2022 Homo sapiens:Dravet syndrome (Ontology Term : 'Dravet syndrome' added !)
- 12:15, 13 December 2021 Homo sapiens:Spina bifida (reference check)
- 08:38, 7 December 2021 Homo sapiens:Spina bifida (Ontology Term : 'folate metabolic pathway' added !)
(Latest | Earliest) View (newer 100) (older 100) (20 | 50 | 100 | 250 | 500)