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.
Details on Person Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma
| Class:Id | LiteratureReference:9606534 |
|---|
| _displayName | Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma |
|---|
| _timestamp | 2018-04-23 17:29:36 |
|---|
| author | [Person:9606541] Forsbring, Monika
[Person:9606538] Vik, Erik S
[Person:9606536] Dalhus, Bjørn
[Person:9606537] Karlsen, Tom H
[Person:9606543] Bergquist, Annika
[Person:9606542] Schrumpf, Erik
[Person:5610066] Bjørås, Magnar
[Person:9606540] Boberg, Kirsten M
[Person:9606544] Alseth, Ingrun |
|---|
| created | [InstanceEdit:9606539] Orlic-Milacic, Marija, 2018-04-23 |
|---|
| journal | Carcinogenesis |
|---|
| pages | 1147-54 |
|---|
| pubMedIdentifier | 19443904 |
|---|
| title | Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma |
|---|
| volume | 30 |
|---|
| year | 2009 |
|---|
| (literatureReference) | [FailedReaction:9605313] Defective MUTYH mutants do not cleave adenine mispaired with 8-oxoguanine [Homo sapiens]
[FailedReaction:9608288] Defective MUTYH mutants do not bind adenine mispaired with 8-oxoguanine [Homo sapiens]
[Pathway:9608290] Defective MUTYH substrate processing [Homo sapiens]
[Pathway:9616334] Defective Base Excision Repair Associated with NEIL1 [Homo sapiens]
[EntityWithAccessionedSequence:9606359] MUTYH-3 R260Q [nucleoplasm] [Homo sapiens]
[EntityWithAccessionedSequence:9616340] NEIL1 G83D [nucleoplasm] [Homo sapiens]
[Summation:9628741] NEIL1 G83D variant is a low frequency polymorphism, estimate...
[Summation:9628757] NEIL1 G83D variant is a low frequency polymorphism, estimate...
[Summation:9628761] NEIL1 G83D variant is a low frequency polymorphism, estimate...
[Summation:9629147] NEIL1 G83D variant is a low frequency polymorphism, estimate... |
|---|
|
[Change default viewing format]
|
No pathways have been reviewed or authored by Catalytically impaired hMYH and NEIL1 mutant proteins identified in patients with primary sclerosing cholangitis and cholangiocarcinoma (9606534)
