User contributions
From WikiPathways
(Latest | Earliest) View (newer 100) (older 100) (20 | 50 | 100 | 250 | 500)
- 16:11, 4 August 2023 Homo sapiens:10q22q23 copy number variation (Ontology Term : 'chromosomal duplication syndrome' added !)
- 16:11, 4 August 2023 Homo sapiens:10q22q23 copy number variation (Ontology Term : 'chromosomal deletion syndrome' added !)
- 16:11, 4 August 2023 Homo sapiens:10q22q23 copy number variation (Ontology Term : 'disease pathway' added !)
- 16:09, 4 August 2023 N Homo sapiens:10q22q23 copy number variation (New pathway)
- 14:11, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (Modified description) (top)
- 14:10, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (Modified description)
- 13:59, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (corrections in progress)
- 12:29, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (correction in progress)
- 12:10, 4 August 2023 Homo sapiens:11p11.2 copy number variation syndrome (correction in progress)
- 17:28, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (Modified description)
- 17:26, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (corrections in progress)
- 16:25, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (correction in progress)
- 14:56, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (correction in progress)
- 14:40, 3 August 2023 Homo sapiens:10q11.21q11.23 copy number variation syndrome (correction in progress)
- 13:39, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress) (top)
- 13:33, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (Modified description)
- 13:32, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (Ontology Term : 'chromosomal deletion syndrome' added !)
- 13:30, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
- 08:59, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
- 07:54, 3 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
- 16:07, 2 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (correction in progress)
- 15:03, 2 August 2023 Homo sapiens:8p23.1 copy number variation syndrome (corrections in progress)
- 14:41, 2 August 2023 Homo sapiens:7q11.23 distal copy number variation (Ontology Term : 'disease pathway' added !)
- 14:40, 2 August 2023 Homo sapiens:7q11.23 distal copy number variation (Modified description)
- 14:35, 2 August 2023 Homo sapiens:7q11.23 distal copy number variation (work in progress)
- 12:16, 2 August 2023 N Homo sapiens:7q11.23 distal copy number variation (New pathway)
- 11:35, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'Down syndrome' added !) (top)
- 11:34, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'melanocortin system pathway' added !)
- 11:34, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'leptin system pathway' added !)
- 11:34, 2 August 2023 Homo sapiens:6q16 copy number variation (Ontology Term : 'disease pathway' added !)
- 11:32, 2 August 2023 N Homo sapiens:6q16 copy number variation (New pathway)
- 10:48, 2 August 2023 Homo sapiens:5q35 copy number variation (Ontology Term : 'disease pathway' added !)
- 10:48, 2 August 2023 Homo sapiens:5q35 copy number variation (Ontology Term : 'Sotos syndrome' added !)
- 10:47, 2 August 2023 Homo sapiens:5q35 copy number variation (Modified description)
- 10:42, 2 August 2023 Homo sapiens:5q35 copy number variation (correction)
- 10:00, 2 August 2023 Homo sapiens:5q35 copy number variation (correction and update in progress)
- 14:01, 1 August 2023 Homo sapiens:5q35 copy number variation (update and correction in progress)
- 10:24, 1 August 2023 Homo sapiens:5q35 copy number variation (correcton and update in progress)
- 16:37, 27 July 2023 Homo sapiens:Smith-Magenis and Potocki-Lupski syndrome copy number variation (correction and update in progress)
- 16:17, 27 July 2023 Homo sapiens:Smith-Magenis and Potocki-Lupski syndrome copy number variation (Ontology Term : 'disease pathway' added !)
- 13:02, 27 July 2023 Homo sapiens:5q35 copy number variation (correction in progress)
- 12:20, 27 July 2023 Homo sapiens:5q35 copy number variation (correction in progress)
- 11:33, 27 July 2023 Homo sapiens:5q35 copy number variation (correction in progress)
- 11:25, 27 July 2023 Homo sapiens:5q35 copy number variation (corrections)
- 10:18, 27 July 2023 Homo sapiens:5q35 copy number variation (corrections)
- 09:49, 27 July 2023 Homo sapiens:5q35 copy number variation (corrections)
- 09:11, 27 July 2023 Homo sapiens:4p16.3 copy number variation (Modified description)
- 09:06, 27 July 2023 Homo sapiens:4p16.3 copy number variation (Ontology Term : 'disease pathway' added !)
- 09:04, 27 July 2023 Homo sapiens:4p16.3 copy number variation (correction and updates)
- 08:45, 27 July 2023 Homo sapiens:4p16.3 copy number variation (correction and updates)
- 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)
(Latest | Earliest) View (newer 100) (older 100) (20 | 50 | 100 | 250 | 500)