User contributions
From WikiPathways
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- 00:24, 30 January 2024 Homo sapiens:Immune infiltration in pancreatic cancer (Ontology Term : 'regulatory T cell' added !)
- 00:24, 30 January 2024 Homo sapiens:Immune infiltration in pancreatic cancer (Ontology Term : 'macrophage' added !)
- 00:23, 30 January 2024 Homo sapiens:Hippo-Merlin signaling dysregulation (Standardize case) (top)
- 00:16, 30 January 2024 Homo sapiens:Hepatitis C and hepatocellular carcinoma (Standardize case)
- 00:10, 30 January 2024 Homo sapiens:FGFR3 signaling in chondrocyte proliferation and terminal differentiation (Remove OMIM IDs from shown label, keep in comments as in all other disease nodes)
- 00:06, 30 January 2024 Homo sapiens:FGFR3 signaling in chondrocyte proliferation and terminal differentiation (Soften disease color)
- 00:02, 30 January 2024 Homo sapiens:FGFR3 signaling in chondrocyte proliferation and terminal differentiation (Ontology Term : 'chondrocyte' added !)
- 00:01, 30 January 2024 Homo sapiens:Ethylmalonic encephalopathy (Soften disease color)
- 23:55, 29 January 2024 Homo sapiens:Glyoxylate metabolism (Soften and use solid-lined rounded rectangles for disease nodes)
- 23:49, 29 January 2024 Homo sapiens:Glycosylation and related congenital defects (Soften disease color, standardize case)
- 23:46, 29 January 2024 Homo sapiens:Glycosylation and related congenital defects (Modified description)
- 23:45, 29 January 2024 Homo sapiens:Gamma-glutamyl cycle for the biosynthesis and degradation of glutathione (Refine legend, soften disease color, standardize case)
- 23:39, 29 January 2024 Homo sapiens:GABA metabolism (aka GHB) (Soften disease, standardize case)
- 23:33, 29 January 2024 Homo sapiens:GABA metabolism (aka GHB) (Ontology Term : 'astrocyte' added !)
- 23:32, 29 January 2024 Homo sapiens:Ethylmalonic encephalopathy (Soften disease color)
- 23:30, 29 January 2024 Homo sapiens:Ether lipid biosynthesis (Soften disease color, standardize case)
- 13:48, 29 January 2024 Homo sapiens:Disorders of galactose metabolism (Soften disease color; standardize case, pathway node shape)
- 13:44, 29 January 2024 Homo sapiens:Disorders of fructose metabolism (Soften color, use standard line thickness in disease nodes; use standard shape in pathway nodes)
- 13:42, 29 January 2024 Homo sapiens:Disorders of bile acid synthesis and biliary transport (Soften disease color)
- 13:39, 29 January 2024 Homo sapiens:Creatine pathway (Soften disease color)
- 13:36, 29 January 2024 Homo sapiens:Ciliopathies (Soften disease color)
- 13:32, 29 January 2024 Homo sapiens:Disorders in ketone body synthesis (Standardize case)
- 13:29, 29 January 2024 Homo sapiens:Disorders in ketone body synthesis (Standardize case, trim node padding)
- 13:24, 29 January 2024 Homo sapiens:Disorders in ketone body synthesis (Soften color, use standard font weight in disease nodes)
- 13:22, 29 January 2024 Homo sapiens:Disorders in ketone body synthesis (Use standard pathway node shape)
- 13:20, 29 January 2024 Homo sapiens:Disorders in ketolysis (Soften disease color, standardize case)
- 13:17, 29 January 2024 Homo sapiens:Degradation pathway of sphingolipids, including diseases (Standardize case)
- 13:09, 29 January 2024 Homo sapiens:Degradation pathway of sphingolipids, including diseases (Soften disease color)
- 04:13, 29 January 2024 Homo sapiens:Vitamin B12 disorders (Modified description)
- 04:11, 29 January 2024 Homo sapiens:Vitamin B12 disorders (Soften disease color, standardize case)
- 04:02, 29 January 2024 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders (Soften disease color, standardize case)
- 03:52, 29 January 2024 Homo sapiens:Pyrimidine metabolism and related diseases (Soften disease color; refine case, size)
- 03:40, 29 January 2024 Homo sapiens:Purine metabolism and related disorders (Standardize case)
- 03:35, 29 January 2024 Homo sapiens:Purine metabolism and related disorders (Soften disease color)
- 03:29, 29 January 2024 Homo sapiens:Hemesynthesis defects and porphyrias (Refine legend)
- 03:26, 29 January 2024 Homo sapiens:Hemesynthesis defects and porphyrias (Use standard color, shape for disease)
- 03:08, 29 January 2024 Homo sapiens:Copper metabolism (Use standard shape, shorten names per convention)
- 03:03, 29 January 2024 Homo sapiens:Copper metabolism (Soften color, use rounded rectangle for disease)
- 02:50, 29 January 2024 Homo sapiens:Copper metabolism (Ontology Term : 'hepatocyte' added !)
- 02:49, 29 January 2024 Homo sapiens:Copper metabolism (Ontology Term : 'enterocyte' added !)
- 02:43, 29 January 2024 Homo sapiens:Urea cycle and associated pathways (Soften disease color, refine nodes)
- 02:28, 29 January 2024 Homo sapiens:Molybdenum cofactor (Moco) biosynthesis (Soften disease color, standardize case)
- 02:23, 29 January 2024 Homo sapiens:Urea cycle and related diseases (Refine legend, nodes; soften disease color)
- 02:13, 29 January 2024 Homo sapiens:Mitochondrial fatty acid oxidation disorders (Use standard rectangle for metabolites, standardize case)
- 02:10, 29 January 2024 Homo sapiens:Mitochondrial fatty acid oxidation disorders (Use rounded rectangle disease node shapes, mitigate overlap, standardize case)
- 01:58, 29 January 2024 Homo sapiens:Tyrosine metabolism and related disorders (Soften disease color) (top)
- 01:55, 29 January 2024 Homo sapiens:Type I collagen synthesis in the context of osteogenesis imperfecta (Soften disease color)
- 01:52, 29 January 2024 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Soften disease color)
- 01:49, 29 January 2024 Homo sapiens:Cholesterol synthesis disorders (Refine legend)
- 01:39, 29 January 2024 Homo sapiens:Cholesterol synthesis disorders (Soften color and use rounded rectangle in disease nodes)
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