Reactome: A Curated Pathway Database

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 Fousteri, Maria (5690488)

DB_ID Name
5696400 Dual Incision in GG-NER
5696398 Nucleotide Excision Repair
5696399 Global Genome Nucleotide Excision Repair (GG-NER)
5696397 Gap-filling DNA repair synthesis and ligation in GG-NER
5696394 DNA Damage Recognition in GG-NER
5696395 Formation of Incision Complex in GG-NER
6781823 Formation of TC-NER Pre-Incision Complex
6781827 Transcription-Coupled Nucleotide Excision Repair (TC-NER)
6782135 Dual incision in TC-NER
6782210 Gap-filling DNA repair synthesis and ligation in TC-NER

Details on Person Fousteri, Maria

Class:IdPerson:5690488
_displayNameFousteri, Maria
_timestamp2017-08-22 20:42:01
affiliation[Affiliation:6797382] Biomedical Sciences Research Center 'Alexander Fleming'
created[InstanceEdit:5690484] Orlic-Milacic, Marija, 2015-04-28
crossReference[DatabaseIdentifier:6797384] ORCID:0000-0003-1729-5899
firstnameMaria
initialM
modified[InstanceEdit:6792684] Orlic-Milacic, Marija, 2015-08-25
[InstanceEdit:6797383] Orlic-Milacic, Marija, 2015-09-09
[InstanceEdit:6797386] Orlic-Milacic, Marija, 2015-09-09
surnameFousteri
(author)[InstanceEdit:6790576] Fousteri, Maria, 2015-08-03
[LiteratureReference:5690482] Replication protein A safeguards genome integrity by controlling NER incision events
[LiteratureReference:5690486] Sealing of chromosomal DNA nicks during nucleotide excision repair requires XRCC1 and DNA ligase III alpha in a cell-cycle-specific manner
[LiteratureReference:5690489] Three DNA polymerases, recruited by different mechanisms, carry out NER repair synthesis in human cells
[LiteratureReference:6781834] Cockayne syndrome A and B proteins differentially regulate recruitment of chromatin remodeling and repair factors to stalled RNA polymerase II in vivo
[LiteratureReference:6781993] UV-sensitive syndrome protein UVSSA recruits USP7 to regulate transcription-coupled repair
[LiteratureReference:6790538] Mammalian transcription-coupled excision repair
[LiteratureReference:6790549] A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair
[LiteratureReference:6790550] Enhanced chromatin dynamics by FACT promotes transcriptional restart after UV-induced DNA damage
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