Reactome: A Curated Pathway Database
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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Pathways reviewed by Christodoulou, John (5432498)

DB_ID Name
9022534 Loss of MECP2 binding ability to 5hmC-DNA
9022538 Loss of MECP2 binding ability to 5mC-DNA
9022537 Loss of MECP2 binding ability to the NCoR/SMRT complex
9022535 Loss of phosphorylation of MECP2 at T308
9022699 MECP2 regulates neuronal receptors and channels
9022707 MECP2 regulates transcription factors
9022927 MECP2 regulates transcription of genes involved in GABA signaling
9022702 MECP2 regulates transcription of neuronal ligands
9022692 Regulation of MECP2 expression and activity
9005891 Loss of function of MECP2 in Rett syndrome
8986944 Transcriptional Regulation by MECP2

Details on Person Christodoulou, John

Class:IdPerson:5432498
_displayNameChristodoulou, John
_timestamp2019-08-16 02:57:56
affiliation[Affiliation:9640592] Murdoch Children's Research Institute
created[InstanceEdit:5432556] May, Bruce, 2014-05-11
crossReference[DatabaseIdentifier:9658531] ORCID:0000-0002-8431-0641
firstnameJohn
initialJ
modified[InstanceEdit:9640593] Orlic-Milacic, Marija, 2019-04-01
[InstanceEdit:9658533] Orlic-Milacic, Marija, 2019-08-16
surnameChristodoulou
(author)[LiteratureReference:5432420] Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation
[LiteratureReference:5638214] Mutations in SLC33A1 cause a lethal autosomal-recessive disorder with congenital cataracts, hearing loss, and low serum copper and ceruloplasmin
[LiteratureReference:9006581] Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype
[LiteratureReference:9615846] RettBASE: Rett syndrome database update
[URL:9615850] http://mecp2.chw.edu.au/
[LiteratureReference:9831596] Origin of the prevalent SFTPB indel g.1549C > GAA (121ins2) mutation causing surfactant protein B (SP-B) deficiency
[LiteratureReference:9865895] Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression
[InstanceEdit:9608114] Christodoulou, John, 2018-08-07
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