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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Name Email address

Pathways reviewed by Harper, J Wade (2859007)

DB_ID Name
8949613 Cristae formation

Details on Person Harper, J Wade

Class:IdPerson:2859007
_displayNameHarper, J Wade
_timestamp2017-08-22 20:44:49
created[InstanceEdit:2859008] Orlic-Milacic, M, 2012-12-18
firstnameJ Wade
initialJW
surnameHarper
(author)[InstanceEdit:8955549] Harper, J Wade, 2017-01-11
[LiteratureReference:5336461] Defining human ERAD networks through an integrative mapping strategy
[LiteratureReference:5634968] Structures of SPOP-substrate complexes: insights into molecular architectures of BTB-Cul3 ubiquitin ligases
[LiteratureReference:5656417] DNA unwinding by ASCC3 helicase is coupled to ALKBH3-dependent DNA alkylation repair and cancer cell proliferation
[LiteratureReference:5685015] A DNA damage response screen identifies RHINO, a 9-1-1 and TopBP1 interacting protein required for ATR signaling
[LiteratureReference:6785967] A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair
[LiteratureReference:6813760] An OBSL1-Cul7Fbxw8 ubiquitin ligase signaling mechanism regulates Golgi morphology and dendrite patterning
[LiteratureReference:8852041] Dual E1 activation systems for ubiquitin differentially regulate E2 enzyme charging
[LiteratureReference:8862518] Parallel SCF adaptor capture proteomics reveals a role for SCFFBXL17 in NRF2 activation via BACH1 repressor turnover
[LiteratureReference:8863290] Dynamics of cullin-RING ubiquitin ligase network revealed by systematic quantitative proteomics
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