User contributions
From WikiPathways
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- 12:08, 27 February 2019 Homo sapiens:Metabolic pathway of LDL, HDL and TG, including diseases (Added more PW linkouts)
- 11:53, 27 February 2019 Homo sapiens:Metabolic pathway of LDL, HDL and TG, including diseases (Added steroid PW links)
- 11:47, 27 February 2019 Homo sapiens:Metabolic pathway of LDL, HDL and TG, including diseases (Updated LDL transport into cell.)
- 09:51, 27 February 2019 Homo sapiens:Metabolic pathway of LDL, HDL and TG, including diseases (Removed weird signs in lit. ref; changed long OMIM linkouts to short ones)
- 09:45, 27 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Removed weird signs in lit. ref; changed long OMIM links to short ones.)
- 19:14, 25 February 2019 Homo sapiens:Metabolic pathway of LDL, HDL and TG, including diseases (Connected diseases to anchors with enzymes, trying to fix test in Jenkins...)
- 19:08, 25 February 2019 Homo sapiens:Cerebral organic acidurias, including diseases (Updated ID for N-acetylaspartate (was annotated with protein ID, not metabolite ID).)
- 15:33, 25 February 2019 Homo sapiens:Cerebral organic acidurias, including diseases (Removed weird signs in lit. ref)
- 14:31, 25 February 2019 Homo sapiens:Glycosylation and related congenital defects (Removed weird signs in lit. ref, part 2)
- 14:26, 25 February 2019 Homo sapiens:Glycosylation and related congenital defects (Removed weird signs in lit. ref, part 1)
- 14:17, 25 February 2019 Homo sapiens:Gamma-glutamyl cycle for the biosynthesis and degradation of glutathione, including diseases (Removed weird signs in lit. ref)
- 09:13, 25 February 2019 Homo sapiens:Regulatory circuits of STAT3 signaling (Added more details about dephosphorylation/phosphorylation modifications.)
- 09:03, 25 February 2019 Homo sapiens:Regulatory circuits of STAT3 signaling (Added some details as requested by Marvin)
- 13:04, 22 February 2019 Homo sapiens:Glycosylation and related congenital defects (Updated Rhea for reaction connected to 30.11 (was undirected), added lit.refs for disease and protein.)
- 12:55, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Connected unconnected line to P450c17)
- 12:54, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Updated OMIM for Aromatase deficiency (was linked to gene iso disease before).)
- 12:51, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'pseudohermaphroditism' added !)
- 12:47, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'congenital adrenal hyperplasia' added !)
- 12:45, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'congenital adrenal hyperplasia pathway' added !)
- 12:44, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'apparent mineralocorticoid excess syndrome pathway' added !)
- 12:43, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'lipoid congenital adrenal hyperplasia pathway' added !)
- 12:43, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'congenital adrenal insufficiency' added !)
- 12:42, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Changed Omim for Cholesterol side-chain cleavage deficiency to correct one (previous OMIM was for gene, not for disease).)
- 12:36, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'apparent mineralocorticoid excess syndrome' added !)
- 12:36, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'apparent mineralocorticoid excess' added !)
- 12:36, 22 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Ontology Term : 'cortisone reductase deficiency' added !)
- 12:24, 22 February 2019 Homo sapiens:Regulatory circuits of STAT3 signaling (Ontology Term : 'regulatory pathway' added !)
- 11:23, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Ontology Term : 'transport pathway' added !)
- 11:20, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Modified title)
- 11:19, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Modified description)
- 11:18, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Remoced wrong comment from BGD2)
- 11:17, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Added lit.refs for ciliopathies)
- 11:14, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Modified description)
- 11:12, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Connected other gene groups to drawing)
- 11:07, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Added more drawings, connected first groups of genes to items in schematics)
- 10:45, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Added transport direction)
- 10:42, 22 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Added some more graphical details from reference)
- 16:32, 21 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Added figure)
- 16:21, 21 February 2019 Homo sapiens:Genes related to primary cilium development (based on CRISPR) (Modified description)
- 16:05, 21 February 2019 N Homo sapiens:Genes related to primary cilium development (based on CRISPR) (New pathway)
- 13:15, 21 February 2019 Homo sapiens:Alternative pathway of fetal androgen synthesis (Changed conversion to modification fot POR catalysed reaction between protein nodes)
- 21:00, 20 February 2019 Homo sapiens:Alternative pathway of fetal androgen synthesis (Ontology Term : 'steroid inherited metabolic disorder' added !)
- 20:58, 20 February 2019 Homo sapiens:Alternative pathway of fetal androgen synthesis (Annotated missing protein Nodes.)
- 20:51, 20 February 2019 Homo sapiens:Alternative pathway of fetal androgen synthesis (Added more Rheas for bottom left part.)
- 20:25, 20 February 2019 Homo sapiens:Alternative pathway of fetal androgen synthesis (Added more Rhea Ids to the right bottom part)
- 17:28, 20 February 2019 Homo sapiens:Alternative pathway of fetal androgen synthesis (Annotated some more reaction with Rhea (top part), added lit. refs, added first disease node.)
- 12:37, 20 February 2019 Homo sapiens:Vitamin A and carotenoid metabolism (Modified description)
- 15:18, 17 February 2019 Homo sapiens:Classical pathway of steroidogenesis with glucocorticoid and mineralocorticoid metabolism (Changed arrows for diseases to graphical lines; small layout changes.)
- 14:49, 17 February 2019 Homo sapiens:Glycosylation and related congenital defects (Typed alpha to avoid weird characters.)
- 14:48, 17 February 2019 Homo sapiens:Glycosylation and related congenital defects (Changed arrows for diseases to graphical lines, small layout changes)
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