User contributions
From WikiPathways
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- 17:45, 3 February 2024 Homo sapiens:Eukaryotic translation initiation (identifier added)
- 17:43, 3 February 2024 Homo sapiens:Eukaryotic translation initiation (eif1 identifier added.)
- 21:32, 2 February 2024 Homo sapiens:TGF-beta signaling in thyroid cells for epithelial-mesenchymal transition (Added protein complex oject and added pathway identifier for SMAD pathway) (top)
- 21:17, 2 February 2024 Homo sapiens:ERK pathway in Huntington's disease (Fixed interation of HTT)
- 20:58, 2 February 2024 Homo sapiens:Electron transport chain: OXPHOS system in mitochondria (fixed interactions)
- 09:56, 19 July 2023 Homo sapiens:Aerobic glycolysis (Datanode clickable.)
- 09:49, 19 July 2023 Homo sapiens:Aerobic glycolysis (Datanodes clickable.)
- 09:47, 19 July 2023 Homo sapiens:Aerobic glycolysis (Made datanodes clickable.)
- 09:45, 19 July 2023 Homo sapiens:Aerobic glycolysis (Made datanodes clickable.)
- 09:43, 19 July 2023 Homo sapiens:Aerobic glycolysis (Made pathway nodes clickable.)
- 09:36, 19 July 2023 Homo sapiens:Primary ovarian insufficiency (Made a datanode clickable.)
- 09:30, 19 July 2023 Homo sapiens:EGFR tyrosine kinase inhibitor resistance (Made datanode clickable.)
- 09:25, 19 July 2023 Homo sapiens:Aerobic glycolysis - simplified (AK enzyme nomenclature added.)
- 09:24, 19 July 2023 Homo sapiens:Aerobic glycolysis - simplified (AK enzyme nomenclature added.)
- 09:21, 19 July 2023 WP4628 (Discussion edited) (top)
- 09:21, 19 July 2023 N WP4628 (Talkpage autocreated when first thread was posted.)
- 09:21, 19 July 2023 N Comment on a reaction (1) (New page: Hi, Thank you for adding this pathway on WikiPathways. I had a question regarding the pyruvate uptake into mitochondria. According to the pathway, pyruvate uptake into mitochondria leads ...) (top)
- 09:14, 19 July 2023 Homo sapiens:Aerobic glycolysis (Data annotation update.)
- 08:37, 19 July 2023 Homo sapiens:Aerobic glycolysis (Ontology Term : 'cancer pathway' added !)
- 14:27, 17 July 2023 Homo sapiens:1p36 copy number variation syndrome (updated literature)
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