User contributions
From WikiPathways
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- 08:41, 19 April 2024 Homo sapiens:Ovarian infertility (connected unconnected lines, created complex for TSC2 and 1) (top)
- 08:37, 19 April 2024 Homo sapiens:Ovarian infertility (added more missing protein IDs)
- 08:33, 19 April 2024 Homo sapiens:Ovarian infertility (Corrected database for FMR1 protein (Uniprot))
- 08:46, 23 January 2024 Homo sapiens:KCNQ2-related epilepsies (changed data nodes to graphical elements in legend) (top)
- 08:42, 23 January 2024 Homo sapiens:Spina bifida (Changed legend labels from data nodes to labels) (top)
- 08:35, 23 January 2024 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis (Annotated missing nodes and changed data nodes to graphical elements)
- 15:05, 21 August 2023 Homo sapiens:8q11.23 (RB1CC1) copy number variation (Ontology Term : 'schizophrenia' added !) (top)
- 15:04, 21 August 2023 Homo sapiens:8q11.23 (RB1CC1) copy number variation (Ontology Term : 'disease pathway' added !)
- 15:04, 21 August 2023 Homo sapiens:8q11.23 (RB1CC1) copy number variation (Modified description)
- 15:00, 21 August 2023 N Homo sapiens:8q11.23 (RB1CC1) copy number variation (New pathway)
- 09:38, 17 August 2023 Homo sapiens:10q22q23 copy number variation (added new complex ID)
- 14:23, 15 August 2023 Homo sapiens:15q24 copy number variation (work in progress) (top)
- 09:00, 11 August 2023 N Homo sapiens:15q24 copy number variation (New pathway)
- 09:25, 9 August 2023 Homo sapiens:17p13.3 (YWHAE) copy number variation (Ontology Term : 'Miller-Dieker lissencephaly syndrome' added !)
- 09:23, 9 August 2023 Homo sapiens:17p13.3 (YWHAE) copy number variation (Ontology Term : 'disease pathway' added !)
- 09:04, 9 August 2023 Homo sapiens:PAFAH1B1 copy number variation (Ontology Term : 'Miller-Dieker lissencephaly syndrome' added !) (top)
- 09:03, 9 August 2023 Homo sapiens:PAFAH1B1 copy number variation (Ontology Term : 'disease pathway' added !)
- 09:00, 9 August 2023 Homo sapiens:PAFAH1B1 copy number variation (Modified description)
- 08:54, 9 August 2023 N Homo sapiens:PAFAH1B1 copy number variation (New pathway)
- 06:20, 9 August 2023 Homo sapiens:Cell cycle (box for pathway)
- 06:16, 9 August 2023 Homo sapiens:Focal adhesion (gave pathway nodes boxes)
- 19:23, 8 August 2023 Homo sapiens:15q25 copy number variation (Ontology Term : 'chromosome 15q25 deletion syndrome' added !)
- 19:23, 8 August 2023 Homo sapiens:15q25 copy number variation (Ontology Term : 'disease pathway' added !)
- 19:22, 8 August 2023 Homo sapiens:15q25 copy number variation (Modified description)
- 19:19, 8 August 2023 N Homo sapiens:15q25 copy number variation (New pathway)
- 08:31, 8 August 2023 Homo sapiens:15q11q13 copy number variation (Ontology Term : 'chromosomal duplication syndrome' added !)
- 08:31, 8 August 2023 Homo sapiens:15q11q13 copy number variation (Ontology Term : 'chromosomal deletion syndrome' added !)
- 08:30, 8 August 2023 Homo sapiens:15q11q13 copy number variation (Ontology Term : 'disease pathway' added !)
- 08:28, 8 August 2023 Homo sapiens:15q11q13 copy number variation (Modified description)
- 08:21, 8 August 2023 N Homo sapiens:15q11q13 copy number variation (New pathway)
- 15:16, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome (legend correction) (top)
- 15:12, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome (Modified description)
- 15:09, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome (Modified description)
- 15:07, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome (update)
- 10:31, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome (update)
- 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation (Ontology Term : 'chromosomal duplication syndrome' added !) (top)
- 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation (Ontology Term : 'chromosomal deletion syndrome' added !)
- 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation (Ontology Term : 'disease pathway' added !)
- 10:00, 7 August 2023 Homo sapiens:13q12.12 copy number variation (Modified description)
- 09:55, 7 August 2023 N Homo sapiens:13q12.12 copy number variation (New pathway)
- 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation (Ontology Term : 'chromosomal duplication syndrome' added !) (top)
- 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation (Ontology Term : 'chromosomal deletion syndrome' added !)
- 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation (Ontology Term : 'PW:0000001' removed !)
- 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation (Ontology Term : 'disease pathway' added !)
- 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation (Ontology Term : 'Pathway Ontology' added !)
- 13:47, 6 August 2023 N Homo sapiens:13q12 or CRYL1 copy number variation (New pathway)
- 13:21, 6 August 2023 Homo sapiens:10q22q23 copy number variation (Modified description)
- 13:20, 6 August 2023 Homo sapiens:10q22q23 copy number variation (Modified description)
- 13:11, 6 August 2023 Homo sapiens:10q22q23 copy number variation (progress save)
- 12:56, 6 August 2023 Homo sapiens:10q22q23 copy number variation (work in progress)
- 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)
- 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 !)
- 14:06, 30 November 2021 Homo sapiens:Inclusion body myositis (added new pathway)
- 13:48, 30 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis (expert curation workshop updates)
- 09:41, 30 November 2021 Homo sapiens:Serine metabolism (boxed pathway node) (top)
- 09:39, 30 November 2021 Homo sapiens:Riboflavin and CoQ disorders (boxed pathway node)
- 09:37, 30 November 2021 Homo sapiens:Ethylmalonic encephalopathy (fixed graphical clash)
- 09:35, 30 November 2021 Homo sapiens:GABA metabolism (aka GHB) (boxed pathway node)
- 09:34, 30 November 2021 Homo sapiens:Proline and hydroxyproline pathways (boxed pathway node)
- 09:33, 30 November 2021 Homo sapiens:Glycine metabolism, including IMDs (boxed pathway nodes)
- 09:31, 30 November 2021 Homo sapiens:Kisspeptin/kisspeptin receptor system in the ovary (boxed pathway nodes)
- 09:29, 30 November 2021 Homo sapiens:Oxysterols derived from cholesterol (boxed pathway node)
- 09:27, 30 November 2021 Homo sapiens:Krebs cycle disorders (boxed pathway node)
- 09:26, 30 November 2021 Homo sapiens:Thiamine metabolic pathways (boxed pathway nodes)
- 09:24, 30 November 2021 Homo sapiens:Vitamin B12 disorders (small graphical change in pathway node)
- 09:21, 30 November 2021 Homo sapiens:MTHFR deficiency (boxed pathway nodes)
- 09:20, 30 November 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders (boxed pathway nodes)
- 09:18, 30 November 2021 Homo sapiens:Tyrosine metabolism and related disorders (boxed pathway node)
- 09:16, 30 November 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (boxed pathway node)
- 09:13, 30 November 2021 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (boxed pathway nodes)
- 09:12, 30 November 2021 Homo sapiens:Thyroid hormones production and peripheral downstream signaling effects (boxed pathway nodes)
- 09:09, 30 November 2021 Homo sapiens:Pyrimidine metabolism and related diseases (boxed pathway nodes)
- 09:08, 30 November 2021 Homo sapiens:Purine metabolism and related disorders (boxed pathway node)
- 09:06, 30 November 2021 Homo sapiens:Overlap between signal transduction pathways contributing to LMNA laminopathies (small graphical change, boxed pathway nodes)
- 09:02, 30 November 2021 Homo sapiens:Influence of laminopathies on Wnt signaling (small graphical change, boxed pathway nodes)
- 08:59, 30 November 2021 Homo sapiens:Lamin A processing pathway (boxed pathway node)
- 08:56, 30 November 2021 Homo sapiens:Joubert syndrome (boxed pathway nodes)
- 08:52, 30 November 2021 Homo sapiens:Hippo signaling regulation pathways (boxed pathway nodes)
- 08:51, 30 November 2021 Homo sapiens:Degradation pathway of sphingolipids, including diseases (small graphical change)
- 08:49, 30 November 2021 Homo sapiens:Urea cycle and associated pathways (small graphical change: pathway nodes got rounded rectangles)
- 08:44, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 3 (small graphical change) (top)
- 08:42, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 2 (fixed weird characters in literature list) (top)
- 08:39, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 1 (small layout change) (top)
- 08:37, 30 November 2021 Homo sapiens:Acquired partial lipodystrophy / Barraquer-Simons syndrome (small graphical change)
- 08:34, 30 November 2021 Homo sapiens:Kallmann syndrome (Connected unconnected lines)
- 10:07, 22 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis (Ontology Term : 'inclusion body myositis' added !)
- 10:06, 22 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis (converted protein to metabolite)
- 13:13, 11 October 2021 Homo sapiens:22q11.2 copy number variation syndrome (Reverted to version '11:20, 17 September 2021' by <a href="/index.php/User:Fehrhart" title="User:Fehrhart">Fehrhart</a>)
- 11:20, 17 September 2021 Homo sapiens:22q11.2 copy number variation syndrome (Update HIST1H4A for H4C1)
- 09:24, 17 September 2021 Homo sapiens:Male infertility (Updated SEPT12 label to SEPTIN12) (top)
- 09:07, 17 September 2021 Homo sapiens:Parkinson's disease pathway (Updated SEPT5 to SEPTIN5 label)
- 09:07, 17 September 2021 Homo sapiens:Parkin-ubiquitin proteasomal system pathway (Updated SEPT5 to SEPTIN5 label)
- 09:03, 17 September 2021 Homo sapiens:Apoptosis modulation and signaling (Updated ARTS to actual gene symbol SEPTIN4 with an ENSID)
- 12:19, 5 July 2021 Homo sapiens:Network map of SARS-CoV-2 signaling pathway (Ontology Term : 'disease pathway' added !)
- 12:18, 5 July 2021 Homo sapiens:Network map of SARS-CoV-2 signaling pathway (Ontology Term : 'severe acute respiratory syndrome' added !)
- 08:15, 22 June 2021 Homo sapiens:Inclusion body myositis (Modified description)
- 08:14, 22 June 2021 Homo sapiens:Inclusion body myositis (work in progress)
- 08:12, 22 June 2021 Homo sapiens:Inclusion body myositis (Ontology Term : 'muscle cell' added !)
- 08:12, 22 June 2021 Homo sapiens:Inclusion body myositis (Ontology Term : 'inclusion body myositis' added !)
- 08:12, 22 June 2021 Homo sapiens:Inclusion body myositis (Ontology Term : 'disease pathway' added !)
- 08:10, 22 June 2021 Homo sapiens:Inclusion body myositis (work in progress)
- 08:09, 22 June 2021 N Homo sapiens:Inclusion body myositis (New pathway)
- 06:42, 17 June 2021 Homo sapiens:Congenital generalized lipodystrophy (changed a few unreviewed Uniprot IDs to something reviewed)
- 06:33, 17 June 2021 Homo sapiens:Congenital generalized lipodystrophy (Checked and corrected a few interactions)
- 07:01, 7 June 2021 Homo sapiens:TCA cycle in senescence (added ID for ROS)
- 06:55, 7 June 2021 Homo sapiens:Pentose phosphate pathway in senescent cells (made pathway nodes clickable by adding shapes)
- 06:52, 7 June 2021 Homo sapiens:NAD metabolism in oncogene-induced senescence and mitochondrial dysfunction-associated senescence (connected unconnected connections and gave pathway nodes shapes) (top)
- 06:48, 7 June 2021 Homo sapiens:Kynurenine pathway and links to cell senescence (connected unconnected connection and gave pathway nodes shapes)
- 06:45, 7 June 2021 Homo sapiens:Glycolysis in senescence (connected unconnected connection)
- 11:39, 2 June 2021 RareDisease/FeaturedPathways (top)
- 11:37, 2 June 2021 RareDisease/News
- 11:34, 2 June 2021 Homo sapiens:Nucleotide excision repair in xeroderma pigmentosum (Ontology Term : 'xeroderma pigmentosum' added !)
- 11:33, 2 June 2021 Homo sapiens:Nucleotide excision repair in xeroderma pigmentosum (Modified title)
- 06:37, 2 June 2021 Homo sapiens:7q11.23 copy number variation syndrome (connected unconnected line)
- 15:59, 1 June 2021 Homo sapiens:Development of ureteric collection system (Ontology Term : 'CAKUT' added !) (top)
- 15:58, 1 June 2021 Homo sapiens:Nephrogenesis (Ontology Term : 'CAKUT' added !) (top)
- 15:58, 1 June 2021 Homo sapiens:Genes controlling nephrogenesis (Ontology Term : 'CAKUT' added !)
- 15:56, 1 June 2021 Homo sapiens:Nephrogenesis (added WNT4 interaction with WNT3A)
- 15:50, 1 June 2021 Homo sapiens:Development of ureteric collection system (added PBX1)
- 15:48, 1 June 2021 Homo sapiens:GDNF/RET signaling axis (added reference for EYA1)
- 15:45, 1 June 2021 Homo sapiens:Genes controlling nephrogenesis (added reference for EYA1)
- 15:44, 1 June 2021 Homo sapiens:Development of ureteric collection system (added reference for EYA1)
- 15:42, 1 June 2021 Homo sapiens:GDNF/RET signaling axis (added literature for SALL1)
- 15:41, 1 June 2021 Homo sapiens:GDNF/RET signaling axis (added literature for SALL1/EYA1/PAX2 regulation on GDNF)
- 15:38, 1 June 2021 Homo sapiens:Development of ureteric collection system (update SIX1 and EYA1 information)
- 15:23, 1 June 2021 Homo sapiens:Genes controlling nephrogenesis (added information and literature for HNF1B and LHX1)
- 15:13, 1 June 2021 Homo sapiens:GDNF/RET signaling axis (added literature)
- 14:58, 1 June 2021 Homo sapiens:Development of ureteric collection system
- 14:47, 1 June 2021 Homo sapiens:Development of ureteric collection system (updated with BMP pathway information)
- 11:35, 31 May 2021 Homo sapiens:Meta pathway lipodystrophy, dyslipidemia and hyperlipidemia (Ontology Term : 'disease pathway' added !)
- 11:34, 31 May 2021 Homo sapiens:Meta pathway lipodystrophy, dyslipidemia and hyperlipidemia (Ontology Term : 'PW:0000001' removed !)
- 11:33, 31 May 2021 Homo sapiens:Progeria-associated lipodystrophy (Ontology Term : 'lipodystrophy' added !)
- 11:25, 31 May 2021 Homo sapiens:Progeria-associated lipodystrophy (Ontology Term : 'PW:0000001' removed !)
- 11:25, 31 May 2021 Homo sapiens:Progeria-associated lipodystrophy (Ontology Term : 'disease pathway' added !)
- 13:54, 28 May 2021 RareDisease/FeaturedPathways
- 13:52, 28 May 2021 RareDisease/News
- 13:49, 28 May 2021 RareDisease/FeaturedPathways
- 13:47, 28 May 2021 RareDisease/News
- 13:44, 28 May 2021 RareDisease/News
- 13:43, 28 May 2021 RareDisease/FeaturedPathways
- 13:40, 28 May 2021 RareDisease/FeaturedPathways
- 13:38, 28 May 2021 RareDisease/News
- 13:36, 28 May 2021 Homo sapiens:Serine metabolism (adapted disease node graphics to the one in the legend)
- 10:46, 28 May 2021 RareDisease/News
- 10:45, 28 May 2021 RareDisease/FeaturedPathways
- 10:44, 28 May 2021 RareDisease/FeaturedPathways
- 10:14, 28 May 2021 RareDisease/News
- 09:44, 28 May 2021 RareDisease/FeaturedPathways
- 09:41, 28 May 2021 RareDisease/FeaturedPathways
- 09:37, 28 May 2021 RareDisease/News
- 09:29, 28 May 2021 RareDisease/SpecialIssue
- 09:26, 28 May 2021 RareDisease/FeaturedPathways
- 09:19, 28 May 2021 RareDisease/FeaturedPathways (→Inborn errors of metabolism)
- 09:15, 28 May 2021 RareDisease/News
- 15:17, 27 May 2021 Caenorhabditis elegans:Fatty acid beta-oxidation 2 (added metabolite identifiers)
- 15:07, 27 May 2021 Caenorhabditis elegans:Fatty acid beta-oxidation 2 (added anchors and catalysis)
- 15:02, 27 May 2021 Caenorhabditis elegans:Fatty acid beta-oxidation 3 (added catalysis, anchors and metabolite identifiers)
- 14:54, 27 May 2021 Caenorhabditis elegans:Fatty acid biosynthesis (connected line, added metabolite identifiers and proper catalysis and anchors)
- 14:39, 27 May 2021 Caenorhabditis elegans:Glycogen metabolism (replaced metabolite labels with metabolite nodes, connected lines) (top)
- 14:25, 27 May 2021 Caenorhabditis elegans:mRNA processing (converted graphical lines)
- 14:20, 27 May 2021 Caenorhabditis elegans:mRNA processing (converted graphical lines)
- 14:14, 27 May 2021 Caenorhabditis elegans:Translation factors (fixed unconnected line)
- 12:44, 29 April 2021 Homo sapiens:Neuroinflammation and glutamatergic signaling (Ontology Term : 'signaling pathway pertinent to the brain and nervous system' added !)
- 14:56, 15 April 2021 Homo sapiens:22q11.2 copy number variation syndrome (added literature reference)
- 11:19, 22 March 2021 RareDisease (top)
- 11:18, 22 March 2021 RareDisease/SpecialIssue
- 16:10, 18 March 2021 Homo sapiens:FOXP3 in COVID-19 (graphical adjustments)
- 16:02, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (Modified title)
- 16:01, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (Ontology Term : 'severe acute respiratory syndrome' added !)
- 16:01, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (Ontology Term : 'disease pathway' added !)
- 16:00, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (small graphical adaptions)
- 15:10, 18 March 2021 Homo sapiens:SARS-CoV-2 and COVID-19 pathway (added S2 identifiers)
- 14:53, 18 March 2021 Homo sapiens:SARS-CoV-2 innate immunity evasion and cell-specific immune response (fixed unconnected lines, added S1 ID)
- 14:43, 18 March 2021 Homo sapiens:Mitochondrial immune response to SARS-CoV-2 (Updated S1/S2 identifiers)
- 14:32, 18 March 2021 Homo sapiens:SARS-CoV-2 altering angiogenesis via NRP1 (added IDs for S1 and S2)
- 08:37, 12 March 2021 Homo sapiens:15q13.3 copy number variation syndrome (update in progress) (top)
- 08:32, 12 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (fixed unconnected line)
- 08:29, 12 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (update in progress)
- 08:09, 12 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (update in progress)
- 07:45, 12 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (graphical update)
- 16:19, 11 March 2021 Homo sapiens:16p11.2 distal deletion syndrome (update in progress)
- 16:08, 11 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 15:48, 11 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 15:46, 11 March 2021 Homo sapiens:22q11.2 copy number variation syndrome (updated to GRCH37)
- 15:26, 11 March 2021 Homo sapiens:16p11.2 distal deletion syndrome (Modified description)
- 15:24, 11 March 2021 Homo sapiens:16p11.2 distal deletion syndrome (update to GHRCh37)
- 15:17, 11 March 2021 Homo sapiens:16p11.2 proximal deletion syndrome (Modified description)
- 14:01, 11 March 2021 Homo sapiens:15q13.3 copy number variation syndrome (Modified description)
- 14:00, 11 March 2021 Homo sapiens:15q13.3 copy number variation syndrome (update to GHRC37)
- 13:44, 11 March 2021 Homo sapiens:15q11.2 copy number variation syndrome (Modified description)
- 13:43, 11 March 2021 Homo sapiens:15q11.2 copy number variation syndrome (updated to GRCh37)
- 13:39, 11 March 2021 Homo sapiens:3q29 copy number variation syndrome (update to GRCh37)
- 13:37, 11 March 2021 Homo sapiens:1q21.1 copy number variation syndrome (update to GRCh37)
- 13:13, 11 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (Modified description)
- 13:11, 11 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (update in progress)
- 13:04, 11 March 2021 Homo sapiens:7q11.23 copy number variation syndrome (update according to GRCh37/hg19)
- 12:42, 11 March 2021 Homo sapiens:3q29 copy number variation syndrome (Modified description)
- 12:40, 11 March 2021 Homo sapiens:3q29 copy number variation syndrome (updated breakpoints)
- 12:31, 11 March 2021 Homo sapiens:1q21.1 copy number variation syndrome (Modified description)
- 12:28, 11 March 2021 Homo sapiens:1q21.1 copy number variation syndrome (corrected break point positions)
- 12:14, 10 March 2021 Homo sapiens:Kallmann syndrome (Ontology Term : 'disease pathway' added !)
- 08:10, 8 March 2021 Homo sapiens:FOXP3 in COVID-19 (connected unconnected line)
- 08:08, 8 March 2021 Homo sapiens:FOXA2 pathway (connected unconnected line)
- 16:13, 26 February 2021 Homo sapiens:Development of ureteric collection system (minor graphical adjustment)
- 12:14, 17 February 2021 RareDisease/News
- 12:13, 17 February 2021 Homo sapiens:Development of ureteric collection system (added TGFB2 and references)
- 11:53, 17 February 2021 Homo sapiens:Development of ureteric collection system (added new reference)
- 11:47, 17 February 2021 Homo sapiens:Development of ureteric collection system (work in progress)
- 14:41, 11 February 2021 Homo sapiens:Development of ureteric collection system (fixed unconnected line)
- 14:40, 11 February 2021 Homo sapiens:Development of ureteric collection system (Modified description)
- 14:37, 11 February 2021 Homo sapiens:Development of ureteric collection system (work in progress)
- 14:28, 11 February 2021 Homo sapiens:Development of ureteric collection system (Modified title)
- 18:37, 9 February 2021 Homo sapiens:Development of ureteric collection system (work in progress)
- 18:30, 9 February 2021 Homo sapiens:Development of ureteric collection system (work in progress)
- 18:15, 9 February 2021 Homo sapiens:Development of ureteric collection system (work in progress)
- 16:49, 9 February 2021 Homo sapiens:SARS-CoV-2 and COVID-19 pathway (Added peer reviewed paper to preprint version of reference)
- 09:28, 9 February 2021 RareDisease/FeaturedPathways (→CAKUT (congenital anomalies of the kidney and urinary tract))
- 09:28, 9 February 2021 RareDisease/FeaturedPathways (→Rare diseases in general)
- 09:27, 9 February 2021 RareDisease/News
- 09:18, 8 February 2021 Homo sapiens:Development of ureteric collection system (Modified description)
- 09:18, 8 February 2021 Homo sapiens:Nephrogenesis (Modified description)
- 09:17, 8 February 2021 RareDisease/FeaturedPathways (→CAKUT (congenital anomalies of the kidney and urinary tract))
- 09:13, 8 February 2021 RareDisease/News
- 09:02, 8 February 2021 Homo sapiens:Nephrogenesis (Ontology Term : 'kidney disease' added !)
- 09:02, 8 February 2021 Homo sapiens:Nephrogenesis (Ontology Term : 'Notch signaling pathway' added !)
- 09:01, 8 February 2021 Homo sapiens:Nephrogenesis (Ontology Term : 'signaling pathway' added !)
- 09:01, 8 February 2021 Homo sapiens:Development of ureteric collection system (Ontology Term : 'kidney disease' added !)
- 09:01, 8 February 2021 Homo sapiens:Development of ureteric collection system (Ontology Term : 'signaling pathway' added !)
- 08:48, 8 February 2021 N Homo sapiens:Development of ureteric collection system (New pathway)
- 08:47, 8 February 2021 N Homo sapiens:Nephrogenesis (New pathway)
- 15:42, 4 February 2021 Homo sapiens:Genes controlling nephrogenesis (CAKUT expert curation round 1)
- 10:54, 4 February 2021 Homo sapiens:Genes controlling nephrogenesis (Modified title)
- 17:46, 2 February 2021 Homo sapiens:SARS-CoV-2 innate immunity evasion and cell-specific immune response (Corrected some identifiers)
- 17:17, 2 February 2021 Homo sapiens:SARS-CoV-2 innate immunity evasion and cell-specific immune response (Untangled tangles, corrected some IDs)
- 16:57, 2 February 2021 Homo sapiens:Mitochondrial immune response to SARS-CoV-2 (Corrected some graphical standards (metabolite = blue) and IDs)
- 14:51, 25 January 2021 Homo sapiens:Mitochondrial immune response to SARS-CoV-2
- 12:51, 18 January 2021 RareDisease/SpecialIssue
- 13:06, 11 January 2021 Homo sapiens:nsp1 from SARS-CoV-2 inhibits translation initiation in the host cell (Ontology Term : 'viral infectious disease' added !)
- 13:05, 11 January 2021 Homo sapiens:nsp1 from SARS-CoV-2 inhibits translation initiation in the host cell (Ontology Term : 'severe acute respiratory syndrome' added !)
- 15:36, 17 December 2020 Mus musculus:Toll-like receptor signaling pathway (connect unconnected lines)
- 15:29, 17 December 2020 Mus musculus:Endochondral ossification (connected lines)
- 15:25, 17 December 2020 Mus musculus:Selenium metabolism / selenoproteins (connected lines)
- 15:19, 17 December 2020 Mus musculus:mRNA processing (connected lines)
- 15:05, 17 December 2020 Mus musculus:TGF-beta signaling pathway (connected unconnected line)
- 15:02, 17 December 2020 Mus musculus:Myometrial relaxation and contraction pathways (connected unconnected lines)
- 15:00, 17 December 2020 Mus musculus:Prostaglandin synthesis and regulation (added reference mentioned in description)
- 14:59, 17 December 2020 Mus musculus:Prostaglandin synthesis and regulation (connected line)
- 14:51, 17 December 2020 Mus musculus:Complement and coagulation cascades (connected lines)
- 11:05, 7 December 2020 Homo sapiens:22q11.2 copy number variation syndrome (corrected a typo)
- 16:32, 3 December 2020 Homo sapiens:Prader-Willi and Angelman syndrome (updated IPW ID and color (RNA))
- 15:55, 3 December 2020 Homo sapiens:22q11.2 copy number variation syndrome (added breakpoints LCR22A-D)
- 11:33, 3 December 2020 Homo sapiens:22q11.2 copy number variation syndrome (major update done)
- 10:57, 3 December 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 10:48, 3 December 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 16:41, 30 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 16:31, 30 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 08:50, 30 November 2020 Homo sapiens:CAMKK2 pathway (connected some of the unconnected lines)
- 08:46, 30 November 2020 Homo sapiens:Cholesterol biosynthesis with skeletal dysplasias (Ontology Term : 'genetic disease' added !)
- 08:41, 30 November 2020 Homo sapiens:Diclofenac metabolic pathway (Ontology Term : 'Disease' added !)
- 08:29, 30 November 2020 Homo sapiens:RAS and bradykinin pathways in COVID-19 (Ontology Term : 'disease pathway' added !)
- 08:29, 30 November 2020 Homo sapiens:RAS and bradykinin pathways in COVID-19 (Ontology Term : 'viral infectious disease' added !)
- 08:29, 30 November 2020 Homo sapiens:RAS and bradykinin pathways in COVID-19 (Ontology Term : 'severe acute respiratory syndrome' added !)
- 08:28, 30 November 2020 Homo sapiens:RAS and bradykinin pathways in COVID-19 (small graphical adaptions)
- 08:26, 30 November 2020 Homo sapiens:STING pathway in Kawasaki-like disease and COVID-19 (Modified description)
- 15:39, 27 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 15:10, 27 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 08:59, 17 November 2020 Homo sapiens:SARS-CoV-2 and COVID-19 pathway (small graphical updates)
- 08:30, 17 November 2020 Homo sapiens:1q21.1 copy number variation syndrome (format update for pathway node)
- 14:49, 16 November 2020 Homo sapiens:7q11.23 copy number variation syndrome (Corrected typo)
- 20:50, 9 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (Update in progress)
- 15:06, 9 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 10:08, 4 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update)
- 08:18, 4 November 2020 Homo sapiens:16p11.2 proximal deletion syndrome (connected unconnected lines)
- 08:17, 4 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update)
- 08:01, 4 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update)
- 14:24, 3 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (update legend)
- 13:55, 3 November 2020 Homo sapiens:22q11.2 copy number variation syndrome (Update)
- 15:58, 29 October 2020 Homo sapiens:Aspirin and miRNAs (added node IDs)
- 10:30, 29 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (first complete draft done)
- 10:19, 29 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 09:34, 29 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 13:14, 28 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 15:22, 22 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 15:03, 22 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 09:01, 22 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 10:24, 20 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 10:08, 20 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (converted legend to graphical line)
- 10:07, 20 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 09:36, 20 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 13:25, 15 October 2020 Homo sapiens:Metabolism of angiotensinogen to angiotensins (fixed screwed up complex graphics for this version)
- 13:14, 15 October 2020 Homo sapiens:LDLRAD4 and what we know about it (updated miR nomenclature and WP style)
- 13:08, 15 October 2020 Homo sapiens:Perturbations to host-cell autophagy, induced by SARS-CoV-2 proteins (fixed unconnected lines)
- 13:15, 9 October 2020 Homo sapiens:Glucocorticoid receptor pathway
- 13:14, 9 October 2020 Homo sapiens:Glucocorticoid receptor pathway
- 13:02, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 12:14, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 11:34, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 11:05, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 10:16, 9 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 15:03, 8 October 2020 Homo sapiens:16p11.2 proximal deletion syndrome (work in progress)
- 14:07, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (first draft finished)
- 13:38, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 12:52, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 12:35, 8 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 16:22, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 15:24, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 12:42, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 11:54, 1 October 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 09:34, 1 October 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 09:22, 1 October 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 08:54, 25 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 08:05, 25 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 15:52, 21 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 15:41, 21 September 2020 Homo sapiens:16p11.2 distal deletion syndrome (work in progress)
- 08:36, 18 September 2020 RareDisease/FeaturedPathways (→Copy number variation syndromes)
- 08:35, 18 September 2020 RareDisease/News
- 14:37, 17 September 2020 Homo sapiens:7q11.23 copy number variation syndrome (Modified description)
- 14:36, 17 September 2020 Homo sapiens:7q11.23 copy number variation syndrome (Modified title)
- 14:35, 17 September 2020 Homo sapiens:22q11.2 copy number variation syndrome (Modified title)
- 12:43, 25 August 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 11:56, 25 August 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 11:16, 25 August 2020 Homo sapiens:22q11.2 copy number variation syndrome (update in progress)
- 07:11, 21 August 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 07:03, 21 August 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 13:58, 20 August 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 13:14, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Modified description)
- 13:05, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Ontology Term : 'disease pathway' added !)
- 13:04, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Ontology Term : 'chromosome 15q13.3 microdeletion syndrome' added !)
- 13:03, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (Ontology Term : 'genetic disease' added !)
- 13:00, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 09:06, 20 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 12:19, 19 August 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 08:59, 28 July 2020 RareDisease/FeaturedPathways
- 08:56, 28 July 2020 RareDisease/News
- 08:21, 28 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 08:10, 28 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 06:28, 28 July 2020 Homo sapiens:7q11.23 copy number variation syndrome (work in progress)
- 16:20, 27 July 2020 Homo sapiens:22q11.2 copy number variation syndrome (Undergoing reconstruction and completion of deleted gene list)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Modified description)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Ontology Term : 'genetic disease' added !)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Ontology Term : 'disease pathway' added !)
- 15:35, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Ontology Term : 'chromosome 16p11.2 deletion syndrome, 220kb' added !)
- 15:34, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Ontology Term : 'chromosome 16p11.2 deletion syndrome, 220kb' added !)
- 15:34, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Ontology Term : 'disease pathway' added !)
- 15:34, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Ontology Term : 'genetic disease' added !)
- 15:33, 27 July 2020 Homo sapiens:16p11.2 distal deletion syndrome (Modified description)
- 15:32, 27 July 2020 Homo sapiens:16p11.2 proximal deletion syndrome (Modified description)
- 15:28, 27 July 2020 N Homo sapiens:16p11.2 distal deletion syndrome (New pathway)
- 15:20, 27 July 2020 N Homo sapiens:16p11.2 proximal deletion syndrome (New pathway)
- 15:54, 23 July 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 15:16, 23 July 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
- 11:18, 22 July 2020 Homo sapiens:15q13.3 copy number variation syndrome (work in progress)
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