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• 13:27, 17 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Added lit. ref for CSAT conversion.) (top)
• 13:20, 17 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Added rhea ID for homocysteine -> methionine interaction.)
• 13:18, 17 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Updated ID for MS to Uniprot.)
• 13:15, 17 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Added rhea for CySD interaction, updated Uniprot ID to reviewed.)
• 13:01, 17 January 2021 IEM/CoveredPathways‎ (top)
• 12:58, 17 January 2021 IEM/CoveredPathways‎
• 12:55, 17 January 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine‎ (Added small textual details) (top)
• 15:38, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Updated complex vis. in legend.)
• 15:36, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Updated visual style of PW for webview.)
• 15:34, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Added two more alternative names for disease nodes.)
• 15:33, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'hypermethioninemia due to adenosine kinase deficiency' added !)
• 15:32, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'isolated sulfite oxidase deficiency' added !)
• 15:31, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (alt. name for Cystathionine beta-synthase deficiency.)
• 15:30, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'cystathioninuria pathway' added !)
• 15:30, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'cystathioninuria' added !)
• 15:28, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'homocystinuria pathway' added !)
• 15:28, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'homocystinuria' added !)
• 15:26, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Added alt. name for MAT deficiency.)
• 15:24, 10 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur 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) (top)
• 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 Sulphur 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 Sulphur Amino Acids and related disorders‎ (Added info on SAHH deficiency.)
• 16:37, 9 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur 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 Sulphur Amino Acids and related disorders‎ (Ontology Term : 'hypermethioninemia' added !)
• 16:35, 9 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'hypermethioninemia pathway' added !)
• 16:35, 9 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur Amino Acids and related disorders‎ (Ontology Term : 'hypermethioninemia pathway' added !)
• 16:34, 9 January 2021 Homo sapiens:Methionine metabolism leading to Sulphur 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 Sulphur Amino Acids and related disorders‎ (Added legend)
• 16:21, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'tyrosinemia pathway' added !) (top)
• 16:21, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'tyrosinemia type II pathway' added !)
• 16:21, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'tyrosinemia type II' added !)
• 16:20, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Fixed typo for Type II.)
• 16:19, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'tyrosinemia type III pathway' added !)
• 16:18, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'tyrosinemia type III' added !)
• 16:18, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'tyrosinemia type I pathway' added !)
• 16:18, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'tyrosinemia type I' added !)
• 16:17, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Ontology Term : 'PW:0000013' removed !)
• 16:17, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (Added biomarker vis. to legend.)
• 16:14, 9 January 2021 Homo sapiens:Tyrosine Metabolism‎ (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)

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