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• 10:03, 7 November 2024 Homo sapiens:Dravet syndrome‎ (Added SNTA1) (top)
• 08:43, 22 August 2024 Homo sapiens:Development of ureteric derived collecting system‎ (update) (top)
• 08:41, 22 August 2024 Homo sapiens:GDNF/RET signaling axis‎ (Update) (top)
• 14:07, 21 August 2024 Homo sapiens:GDNF/RET signaling axis‎ (update with more actual information and graphical improvement)
• 13:59, 21 August 2024 Homo sapiens:Development of ureteric derived collecting system‎ (update with more actual literature)
• 13:37, 21 August 2024 Homo sapiens:GDNF/RET signaling axis‎
• 08:41, 19 April 2024 Homo sapiens:Ovarian infertility‎ (connected unconnected lines, created complex for TSC2 and 1)
• 08:37, 19 April 2024 Homo sapiens:Ovarian infertility‎ (added more missing protein IDs)
• 08:33, 19 April 2024 Homo sapiens:Ovarian infertility‎ (Corrected database for FMR1 protein (Uniprot))
• 08:46, 23 January 2024 Homo sapiens:KCNQ2-related epilepsies‎ (changed data nodes to graphical elements in legend) (top)
• 08:42, 23 January 2024 Homo sapiens:Spina bifida‎ (Changed legend labels from data nodes to labels)
• 08:35, 23 January 2024 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis‎ (Annotated missing nodes and changed data nodes to graphical elements)
• 15:05, 21 August 2023 Homo sapiens:8q11.23 (RB1CC1) copy number variation‎ (Ontology Term : 'schizophrenia' added !)
• 15:04, 21 August 2023 Homo sapiens:8q11.23 (RB1CC1) copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 15:04, 21 August 2023 Homo sapiens:8q11.23 (RB1CC1) copy number variation‎ (Modified description)
• 15:00, 21 August 2023 N Homo sapiens:8q11.23 (RB1CC1) copy number variation‎ (New pathway)
• 09:38, 17 August 2023 Homo sapiens:10q22q23 copy number variation‎ (added new complex ID)
• 14:23, 15 August 2023 Homo sapiens:15q24 copy number variation‎ (work in progress) (top)
• 09:00, 11 August 2023 N Homo sapiens:15q24 copy number variation‎ (New pathway)
• 09:25, 9 August 2023 Homo sapiens:17p13.3 (YWHAE) copy number variation‎ (Ontology Term : 'Miller-Dieker lissencephaly syndrome' added !)
• 09:23, 9 August 2023 Homo sapiens:17p13.3 (YWHAE) copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 09:04, 9 August 2023 Homo sapiens:PAFAH1B1 copy number variation‎ (Ontology Term : 'Miller-Dieker lissencephaly syndrome' added !)
• 09:03, 9 August 2023 Homo sapiens:PAFAH1B1 copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 09:00, 9 August 2023 Homo sapiens:PAFAH1B1 copy number variation‎ (Modified description)
• 08:54, 9 August 2023 N Homo sapiens:PAFAH1B1 copy number variation‎ (New pathway)
• 06:20, 9 August 2023 Homo sapiens:Cell cycle‎ (box for pathway)
• 06:16, 9 August 2023 Homo sapiens:Focal adhesion‎ (gave pathway nodes boxes)
• 19:23, 8 August 2023 Homo sapiens:15q25 copy number variation‎ (Ontology Term : 'chromosome 15q25 deletion syndrome' added !)
• 19:23, 8 August 2023 Homo sapiens:15q25 copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 19:22, 8 August 2023 Homo sapiens:15q25 copy number variation‎ (Modified description)
• 19:19, 8 August 2023 N Homo sapiens:15q25 copy number variation‎ (New pathway)
• 08:31, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Ontology Term : 'chromosomal duplication syndrome' added !)
• 08:31, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Ontology Term : 'chromosomal deletion syndrome' added !)
• 08:30, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 08:28, 8 August 2023 Homo sapiens:15q11q13 copy number variation‎ (Modified description)
• 08:21, 8 August 2023 N Homo sapiens:15q11q13 copy number variation‎ (New pathway)
• 15:16, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (legend correction)
• 15:12, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (Modified description)
• 15:09, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (Modified description)
• 15:07, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (update)
• 10:31, 7 August 2023 Homo sapiens:Prader-Willi and Angelman syndrome‎ (update)
• 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Ontology Term : 'chromosomal duplication syndrome' added !)
• 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Ontology Term : 'chromosomal deletion syndrome' added !)
• 10:03, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Ontology Term : 'disease pathway' added !)
• 10:00, 7 August 2023 Homo sapiens:13q12.12 copy number variation‎ (Modified description)
• 09:55, 7 August 2023 N Homo sapiens:13q12.12 copy number variation‎ (New pathway)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'chromosomal duplication syndrome' added !)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'chromosomal deletion syndrome' added !)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'PW:0000001' removed !)
• 13:49, 6 August 2023 Homo sapiens:13q12 or CRYL1 copy number variation ‎ (Ontology Term : 'disease pathway' added !)

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