User contributions
From WikiPathways
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- 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
- 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 (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)
- 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)
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