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• 15:26, 10 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Added alt. name for MAT deficiency.)
• 15:24, 10 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Ontology Term : 'cysteine and methionine metabolic pathway' added !)
• 15:23, 10 January 2021 IEM/CoveredPathways‎
• 15:21, 10 January 2021 Homo sapiens:Vitamin B12 disorders‎ (Added legend)
• 15:18, 10 January 2021 Homo sapiens:Vitamin B12 disorders‎ (Typo fix for methionine)
• 15:17, 10 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Added some alternative names for diseases as comments; checked all OMIM IDs.)
• 16:38, 9 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Added info on SAHH deficiency.)
• 16:37, 9 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Ontology Term : 'hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase' added !)
• 16:36, 9 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Ontology Term : 'hypermethioninemia' added !)
• 16:35, 9 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Ontology Term : 'hypermethioninemia pathway' added !)
• 16:35, 9 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Ontology Term : 'hypermethioninemia pathway' added !)
• 16:34, 9 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Added links to Vit. B12 PW from IEM-portal chapter 13 Blau book)
• 16:29, 9 January 2021 Homo sapiens:Methionine metabolism leading to sulfur amino acids and related disorders‎ (Added legend)
• 16:21, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders‎ (Ontology Term : 'tyrosinemia pathway' added !)
• 16:21, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders‎ (Ontology Term : 'tyrosinemia type II pathway' added !)
• 16:21, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders‎ (Ontology Term : 'tyrosinemia type II' added !)
• 16:20, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders‎ (Fixed typo for Type II.)
• 16:19, 9 January 2021 Homo sapiens:Tyrosine metabolism and related disorders‎ (Ontology Term : 'tyrosinemia type III pathway' added !)
• 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)

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