Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

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.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome

Class:IdLiteratureReference:9615839
_displayNameDisrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome
_timestamp2018-08-08 15:00:12
author[Person:9022731] Urdinguio, Rocio G
[Person:9022720] Fernandez, Agustin F
[Person:9022733] Lopez-Nieva, Pilar
[Person:9615840] Rossi, Simona
[Person:9615837] Huertas, Dori
[Person:5340363] Kulis, Marta
[Person:5251168] Liu, Chang-gong
[Person:141493] Croce, CM
[Person:5621670] Calin, George A
[Person:4837336] Esteller, Manel
created[InstanceEdit:9615838] Orlic-Milacic, Marija, 2018-08-08
journalEpigenetics
pages656-63
pubMedIdentifier20716963
titleDisrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome
volume5
year2010
(literatureReference)[Summation:9615836] Based on studies in mice, MECP2 represses IRAK1 gene transcr...
[Change default viewing format]
No pathways have been reviewed or authored by Disrupted microRNA expression caused by Mecp2 loss in a mouse model of Rett syndrome (9615839)