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dc.contributor.authorSharp, A
dc.contributor.authorWelti, J
dc.contributor.authorBlagg, J
dc.contributor.authorde Bono, JS
dc.date.accessioned2017-03-02T11:34:41Z
dc.date.issued2016-09-01
dc.identifier.citationClinical cancer research : an official journal of the American Association for Cancer Research, 2016, 22 (17), pp. 4280 - 4282
dc.identifier.issn1078-0432
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/464
dc.identifier.eissn1557-3265
dc.identifier.doi10.1158/1078-0432.ccr-16-1137
dc.description.abstractAndrogen receptor (AR) splice variants (SV) have been implicated in the development of metastatic castration-resistant prostate cancer and resistance to AR targeting therapies, including abiraterone and enzalutamide. Agents targeting AR-SV are urgently needed to test this hypothesis and further improve the outcome of patients suffering from this lethal disease. Clin Cancer Res; 22(17); 4280-2. ©2016 AACRSee related article by Yang et al., p. 4466.
dc.formatPrint-Electronic
dc.format.extent4280 - 4282
dc.languageeng
dc.language.isoeng
dc.publisherAMER ASSOC CANCER RESEARCH
dc.rights.urihttps://www.rioxx.net/licenses/all-rights-reserved
dc.subjectAnimals
dc.subjectHumans
dc.subjectMice
dc.subjectReceptors, Androgen
dc.subjectAntineoplastic Agents
dc.subjectAlternative Splicing
dc.subjectMale
dc.subjectProtein Interaction Domains and Motifs
dc.subjectMolecular Targeted Therapy
dc.subjectAndrogen Receptor Antagonists
dc.subjectProstatic Neoplasms, Castration-Resistant
dc.titleTargeting Androgen Receptor Aberrations in Castration-Resistant Prostate Cancer.
dc.typeJournal Article
dcterms.dateAccepted2016-05-26
rioxxterms.versionofrecord10.1158/1078-0432.ccr-16-1137
rioxxterms.licenseref.urihttps://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2016-09
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfClinical cancer research : an official journal of the American Association for Cancer Research
pubs.issue17
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Medicinal Chemistry 1
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Translational Therapeutics
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Therapeutics/Medicinal Chemistry 1
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Prostate Cancer Targeted Therapy Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Translational Therapeutics
pubs.publication-statusPublished
pubs.volume22
pubs.embargo.termsNot known
icr.researchteamMedicinal Chemistry 1
icr.researchteamProstate Cancer Targeted Therapy Group
icr.researchteamTranslational Therapeutics
dc.contributor.icrauthorSharp, Adam
dc.contributor.icrauthorDe Bono, Johann


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