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 NEIL3 Repairs Telomere Damage during S Phase to Secure Chromosome Segregation at Mitosis

Class:IdLiteratureReference:9629201
_displayNameNEIL3 Repairs Telomere Damage during S Phase to Secure Chromosome Segregation at Mitosis
_timestamp2018-11-19 19:48:57
author[Person:9009243] Zhou, Jia
[Person:9629196] Chan, Jany
[Person:9629194] Lambelé, Marie
[Person:5687489] Yusufzai, Timur
[Person:9629200] Stumpff, Jason
[Person:9629198] Opresko, Patricia L
[Person:9629202] Thali, Markus
[Person:5655876] Wallace, Susan S
created[InstanceEdit:9629199] Orlic-Milacic, Marija, 2018-11-19
journalCell Rep
pages2044-2056
pubMedIdentifier28854357
titleNEIL3 Repairs Telomere Damage during S Phase to Secure Chromosome Segregation at Mitosis
volume20
year2017
(literatureReference)[Reaction:9629195] NEIL3 recognizes and binds to 5-guanidinohydantoin (Gh) in telomeric DNA [Homo sapiens]
[Reaction:9629216] NEIL3 cleaves 5-guanidinohydantoin (Gh) from damaged telomeric DNA [Homo sapiens]
[Pathway:9629232] Defective Base Excision Repair Associated with NEIL3 [Homo sapiens]
[Summation:9629212] NEIL3 cleaves oxidatively damaged guanine, in the form of 5-...
[Summation:9629231] NEIL3 D132V is a NEIL3 disease variant caused by a missense ...
[Change default viewing format]
No pathways have been reviewed or authored by NEIL3 Repairs Telomere Damage during S Phase to Secure Chromosome Segregation at Mitosis (9629201)