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)
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