User contributions
From WikiPathways
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- 16:18, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders (Ontology Term : 'tyrosinemia type III' added !)
- 16:18, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders (Ontology Term : 'tyrosinemia type I pathway' added !)
- 16:18, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders (Ontology Term : 'tyrosinemia type I' added !)
- 16:17, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders (Ontology Term : 'PW:0000013' removed !)
- 16:17, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders (Added biomarker vis. to legend.)
- 16:14, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders (Added legend.)
- 16:13, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Additional comment for THD (SEGAWA))
- 16:11, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Ontology Term : 'Segawa syndrome pathway' added !)
- 16:11, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Updating OMIM ID for tyrosine hydroxylase deficiency.)
- 16:07, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Ontology Term : 'dystonia 5' added !)
- 16:06, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Ontology Term : 'sepiapterin reductase deficiency' added !)
- 16:06, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Ontology Term : 'megaloblastic anemia' added !)
- 16:04, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Ontology Term : 'PW:0000013' removed !)
- 16:03, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (More updates for readability of full PW.)
- 15:59, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Visual updates for readability)
- 15:56, 9 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (Added legend)
- 21:56, 8 January 2021 IEM/CoveredPathways
- 21:52, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'ubiquinone biosynthetic pathway' added !)
- 21:52, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'primary coenzyme Q10 deficiency 6' added !)
- 21:51, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'primary coenzyme Q10 deficiency 5' added !)
- 21:51, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'primary coenzyme Q10 deficiency 4' added !)
- 21:51, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'primary coenzyme Q10 deficiency 3' added !)
- 21:51, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'primary coenzyme Q10 deficiency 2' added !)
- 21:49, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added another litref for APTX disorder)
- 21:47, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added lit. refs for CoQ2 and APTX related disorders)
- 21:45, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added APTX info and OXPHOS PW link.)
- 21:37, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added lit. ref. for CABC1 disorder)
- 21:35, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added CABC1 info)
- 21:25, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added PDSS1 and 2 info)
- 21:02, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added CoQ10 link to PW)
- 21:00, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added link to PW)
- 20:59, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Connected ubiquinol to CoQ10)
- 20:56, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added CoQ6 and 9)
- 20:40, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added COQ2 details)
- 20:26, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added details on ETFA and B)
- 19:53, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Added more details on ETFDH)
- 19:31, 8 January 2021 Saccharomyces cerevisiae:Glycolysis and gluconeogenesis (Updated duplicate ID for glucose from cas to wikidata)
- 19:31, 8 January 2021 Saccharomyces cerevisiae:Glycolysis and gluconeogenesis (removed genmap comment on clickable link)
- 19:30, 8 January 2021 Saccharomyces cerevisiae:Principal pathways of carbon metabolism (Updated duplicate ID for glucose from cas to wikidata)
- 19:28, 8 January 2021 Rattus norvegicus:Glycolysis and gluconeogenesis (Updated duplicate ID for glucose from cas to wikidata)
- 19:26, 8 January 2021 Drosophila melanogaster:Glycolysis and gluconeogenesis (Updating duplicate cas to wikidata for glucose)
- 19:24, 8 January 2021 Bos taurus:Glycogen metabolism (Updating duplicate cas to wikidata for glucose)
- 15:35, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Removed reactome IDs from interactions.)
- 15:33, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Removed comment from Reactome on RIB translocation.)
- 15:32, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'Brown-Vialetto-Van Laere syndrome 2' added !)
- 15:32, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'Brown-Vialetto-Van Laere syndrome 1' added !)
- 15:31, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'Brown-Vialetto-Van Laere syndrome' added !)
- 15:31, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'coenzyme Q10 deficiency disease' added !)
- 15:31, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'primary coenzyme Q10 deficiency 1' added !)
- 15:31, 8 January 2021 Homo sapiens:Riboflavin and CoQ disorders (Ontology Term : 'riboflavin metabolic pathway' added !)
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