User contributions
From WikiPathways
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- 09:16, 30 November 2021 Homo sapiens:Biosynthesis and regeneration of tetrahydrobiopterin and catabolism of phenylalanine (boxed pathway node)
- 09:13, 30 November 2021 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (boxed pathway nodes)
- 09:12, 30 November 2021 Homo sapiens:Thyroid hormones production and peripheral downstream signaling effects (boxed pathway nodes)
- 09:09, 30 November 2021 Homo sapiens:Pyrimidine metabolism and related diseases (boxed pathway nodes)
- 09:08, 30 November 2021 Homo sapiens:Purine metabolism and related disorders (boxed pathway node)
- 09:06, 30 November 2021 Homo sapiens:Overlap between signal transduction pathways contributing to LMNA laminopathies (small graphical change, boxed pathway nodes)
- 09:02, 30 November 2021 Homo sapiens:Influence of laminopathies on Wnt signaling (small graphical change, boxed pathway nodes)
- 08:59, 30 November 2021 Homo sapiens:Lamin A processing pathway (boxed pathway node)
- 08:56, 30 November 2021 Homo sapiens:Joubert syndrome (boxed pathway nodes)
- 08:52, 30 November 2021 Homo sapiens:Hippo signaling regulation (boxed pathway nodes)
- 08:51, 30 November 2021 Homo sapiens:Degradation pathway of sphingolipids, including diseases (small graphical change)
- 08:49, 30 November 2021 Homo sapiens:Urea cycle and associated pathways (small graphical change: pathway nodes got rounded rectangles)
- 08:44, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 3 (small graphical change)
- 08:42, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 2 (fixed weird characters in literature list)
- 08:39, 30 November 2021 Homo sapiens:Familial hyperlipidemia type 1 (small layout change)
- 08:37, 30 November 2021 Homo sapiens:Acquired partial lipodystrophy / Barraquer-Simons syndrome (small graphical change)
- 08:34, 30 November 2021 Homo sapiens:Kallmann syndrome (Connected unconnected lines)
- 10:07, 22 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis (Ontology Term : 'inclusion body myositis' added !)
- 10:06, 22 November 2021 Homo sapiens:Calcium mediated T-cell apoptosis involved in inclusion body myositis (converted protein to metabolite)
- 13:13, 11 October 2021 Homo sapiens:22q11.2 copy number variation syndrome (Reverted to version '11:20, 17 September 2021' by <a href="/index.php/User:Fehrhart" title="User:Fehrhart">Fehrhart</a>)
- 11:20, 17 September 2021 Homo sapiens:22q11.2 copy number variation syndrome (Update HIST1H4A for H4C1)
- 09:24, 17 September 2021 Homo sapiens:Male infertility (Updated SEPT12 label to SEPTIN12)
- 09:07, 17 September 2021 Homo sapiens:Parkinson's disease pathway (Updated SEPT5 to SEPTIN5 label)
- 09:07, 17 September 2021 Homo sapiens:Parkin-ubiquitin proteasomal system pathway (Updated SEPT5 to SEPTIN5 label)
- 09:03, 17 September 2021 Homo sapiens:Apoptosis modulation and signaling (Updated ARTS to actual gene symbol SEPTIN4 with an ENSID)
- 12:19, 5 July 2021 Homo sapiens:Network map of SARS-CoV-2 signaling (Ontology Term : 'disease pathway' added !)
- 12:18, 5 July 2021 Homo sapiens:Network map of SARS-CoV-2 signaling (Ontology Term : 'severe acute respiratory syndrome' added !)
- 08:15, 22 June 2021 Homo sapiens:Inclusion body myositis (Modified description)
- 08:14, 22 June 2021 Homo sapiens:Inclusion body myositis (work in progress)
- 08:12, 22 June 2021 Homo sapiens:Inclusion body myositis (Ontology Term : 'muscle cell' added !)
- 08:12, 22 June 2021 Homo sapiens:Inclusion body myositis (Ontology Term : 'inclusion body myositis' added !)
- 08:12, 22 June 2021 Homo sapiens:Inclusion body myositis (Ontology Term : 'disease pathway' added !)
- 08:10, 22 June 2021 Homo sapiens:Inclusion body myositis (work in progress)
- 08:09, 22 June 2021 N Homo sapiens:Inclusion body myositis (New pathway)
- 06:42, 17 June 2021 Homo sapiens:Congenital generalized lipodystrophy (changed a few unreviewed Uniprot IDs to something reviewed)
- 06:33, 17 June 2021 Homo sapiens:Congenital generalized lipodystrophy (Checked and corrected a few interactions)
- 07:01, 7 June 2021 Homo sapiens:TCA cycle in senescence (added ID for ROS)
- 06:55, 7 June 2021 Homo sapiens:Pentose phosphate pathway in senescent cells (made pathway nodes clickable by adding shapes)
- 06:52, 7 June 2021 Homo sapiens:NAD metabolism in oncogene-induced senescence and mitochondrial dysfunction-associated senescence (connected unconnected connections and gave pathway nodes shapes)
- 06:48, 7 June 2021 Homo sapiens:Kynurenine pathway and links to cell senescence (connected unconnected connection and gave pathway nodes shapes)
- 06:45, 7 June 2021 Homo sapiens:Glycolysis in senescence (connected unconnected connection)
- 11:39, 2 June 2021 RareDisease/FeaturedPathways (top)
- 11:37, 2 June 2021 RareDisease/News
- 11:34, 2 June 2021 Homo sapiens:Nucleotide excision repair in xeroderma pigmentosum (Ontology Term : 'xeroderma pigmentosum' added !)
- 11:33, 2 June 2021 Homo sapiens:Nucleotide excision repair in xeroderma pigmentosum (Modified title)
- 06:37, 2 June 2021 Homo sapiens:7q11.23 copy number variation syndrome (connected unconnected line)
- 15:59, 1 June 2021 Homo sapiens:Development of ureteric derived collecting system (Ontology Term : 'CAKUT' added !)
- 15:58, 1 June 2021 Homo sapiens:Nephrogenesis (Ontology Term : 'CAKUT' added !)
- 15:58, 1 June 2021 Homo sapiens:Genes controlling nephrogenesis (Ontology Term : 'CAKUT' added !)
- 15:56, 1 June 2021 Homo sapiens:Nephrogenesis (added WNT4 interaction with WNT3A)
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