User contributions
From WikiPathways
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- 21:14, 17 March 2018 Homo sapiens:Pyrimidine metabolism and related diseases (Ontology Term : 'pyrimidine metabolic pathway' added !)
- 21:13, 17 March 2018 Homo sapiens:Pyrimidine metabolism and related diseases (Ontology Term : 'inborn error purine-pyrimidine metabolism disease pathway' added !)
- 21:13, 17 March 2018 Homo sapiens:Purine metabolism and related disorders (Ontology Term : 'purine metabolic pathway' added !)
- 21:12, 17 March 2018 Homo sapiens:Purine metabolism and related disorders (Ontology Term : 'inborn error purine-pyrimidine metabolism disease pathway' added !)
- 21:11, 17 March 2018 Homo sapiens:Pyrimidine metabolism and related diseases (Added lit. ref.)
- 21:08, 17 March 2018 DeSl
- 21:07, 17 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Connected all unconnected lines)
- 21:04, 17 March 2018 Homo sapiens:Purine metabolism and related disorders (Added lit. reference)
- 21:00, 17 March 2018 Homo sapiens:Purine metabolism and related disorders (Changed KEGG genes datasource to Enzyme Nomenclature, removed EC for ID number.)
- 20:58, 17 March 2018 Homo sapiens:Pyrimidine metabolism and related diseases (Changed KEGG genes datasource to Enzyme Nomenclature, removed EC for ID number.)
- 20:56, 17 March 2018 Homo sapiens:Pyrimidine metabolism and related diseases (Added OMIM IDs for diseases)
- 20:55, 17 March 2018 Homo sapiens:Purine metabolism and related disorders (Added OMIM IDs for diseases)
- 16:16, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'neural cell' added !)
- 16:13, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'hyperprolinemia type II disease pathway' added !)
- 16:12, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'hypophosphatasia disease pathway' added !)
- 16:12, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'infantile hypophosphatasia' added !)
- 16:12, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'childhood hypophosphatasia' added !)
- 16:11, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'hypophosphatasia' added !)
- 16:11, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'lysine degradation pathway' added !)
- 16:10, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Ontology Term : 'vitamin B6 metabolic pathway' added !)
- 16:08, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (added last 2 diseases, changed layout a bit more.)
- 15:38, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Modified description)
- 15:37, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Added OMIM IDs for diseases, removed BIND IDs for conversions which were not needed.)
- 15:35, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Modified description)
- 15:25, 16 March 2018 Homo sapiens:Vitamin B6-dependent and responsive disorders (Made various layout changes, added more metabolites+enzymes, changed wrong IDs)
- 14:13, 16 March 2018 DeSl
- 21:34, 15 March 2018 Danio rerio:CRD motif and sFRPs influence on Wnt signaling (Changed gene node to textlabel where needed, slight modification of title.) (top)
- 21:32, 15 March 2018 Danio rerio:CRD motif and sFRPs influence on Wnt signaling (Added more IDs)
- 21:16, 15 March 2018 Danio rerio:CRD motif and sFRPs influence on Wnt signaling (Ontology Term : 'embryonic stem cell' added !)
- 21:11, 15 March 2018 Danio rerio:CRD motif and sFRPs influence on Wnt signaling (Ontology Term : 'Wnt signaling pathway' added !)
- 21:11, 15 March 2018 Danio rerio:CRD motif and sFRPs influence on Wnt signaling (Modified description)
- 21:08, 15 March 2018 N Danio rerio:CRD motif and sFRPs influence on Wnt signaling (New pathway)
- 16:23, 15 March 2018 Danio rerio:Biogenic amine synthesis (Ontology Term : 'dopamine degradation pathway' added !)
- 16:22, 15 March 2018 Danio rerio:Biogenic amine synthesis (Tried to find other gene IDs, but not findable in bridgeDb for species)
- 16:09, 15 March 2018 Danio rerio:Biogenic amine synthesis (Added wikidata as database source where applicable)
- 16:07, 15 March 2018 Danio rerio:Biogenic amine synthesis (Added last IDs needed to annotate full PW.)
- 15:48, 15 March 2018 Danio rerio:Biogenic amine synthesis (Modified description)
- 15:47, 15 March 2018 Danio rerio:Biogenic amine synthesis (Annotated all metabolites.)
- 15:27, 15 March 2018 Danio rerio:Biogenic amine synthesis (Removed "last modified" item)
- 15:26, 15 March 2018 Danio rerio:Biogenic amine synthesis (Connected enzymes to arrows, changed arrows to MIM-conversion, changed layout slightly.)
- 15:59, 7 March 2018 Homo sapiens:Irinotecan pathway (Changed layout)
- 13:29, 1 March 2018 Mus musculus:One-carbon metabolism and related pathways (Removed licence number and last modified part.)
- 13:28, 1 March 2018 Mus musculus:One-carbon metabolism and related pathways (Added small side branch to opthalmate conversion.)
- 08:57, 1 March 2018 Homo sapiens:Neurotransmitter disorders (Modified description)
- 13:46, 23 February 2018 Homo sapiens:Neurotransmitter disorders (Added OMIM IDs for disease)
- 13:43, 23 February 2018 Homo sapiens:Neurotransmitter disorders (Added DISEASE info to node)
- 13:32, 23 February 2018 Homo sapiens:Neurotransmitter disorders (Ontology Term : 'dopamine beta hydroxylase deficiency pathway' added !)
- 13:32, 23 February 2018 Homo sapiens:Neurotransmitter disorders (Ontology Term : 'dopamine beta-hydroxylase deficiency' added !)
- 13:30, 23 February 2018 Homo sapiens:Neurotransmitter disorders (Ontology Term : 'neurotransmitter metabolic pathway' added !)
- 09:23, 23 February 2018 DeSl (→Pathways of Interest)
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