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)
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