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Article: Targeting PI3K Signaling in Cancer: A Cautionary Tale of Two AKTs

TitleTargeting PI3K Signaling in Cancer: A Cautionary Tale of Two AKTs
Authors
Issue Date2016
Citation
Cancer Cell, 2016, v. 29, n. 4, p. 429-431 How to Cite?
Abstract© 2016 Elsevier Inc. AKT inhibitors represent promising therapeutics for cancers with PI3K-AKT pathway hyperactivation. In this issue of Cancer Cell, Wang et al. (2016) report the unexpected finding that ablation of AKT signaling in hepatocytes leads to hepatocellular carcinoma and enhances the incidence of lung metastases in a toxin-induced liver cancer model.
Persistent Identifierhttp://hdl.handle.net/10722/292069
ISSN
2023 Impact Factor: 48.8
2023 SCImago Journal Rankings: 17.507
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorFortin, Jérôme-
dc.contributor.authorMak, Tak W.-
dc.date.accessioned2020-11-17T14:55:42Z-
dc.date.available2020-11-17T14:55:42Z-
dc.date.issued2016-
dc.identifier.citationCancer Cell, 2016, v. 29, n. 4, p. 429-431-
dc.identifier.issn1535-6108-
dc.identifier.urihttp://hdl.handle.net/10722/292069-
dc.description.abstract© 2016 Elsevier Inc. AKT inhibitors represent promising therapeutics for cancers with PI3K-AKT pathway hyperactivation. In this issue of Cancer Cell, Wang et al. (2016) report the unexpected finding that ablation of AKT signaling in hepatocytes leads to hepatocellular carcinoma and enhances the incidence of lung metastases in a toxin-induced liver cancer model.-
dc.languageeng-
dc.relation.ispartofCancer Cell-
dc.titleTargeting PI3K Signaling in Cancer: A Cautionary Tale of Two AKTs-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1016/j.ccell.2016.03.020-
dc.identifier.pmid27070694-
dc.identifier.scopuseid_2-s2.0-84962633169-
dc.identifier.volume29-
dc.identifier.issue4-
dc.identifier.spage429-
dc.identifier.epage431-
dc.identifier.eissn1878-3686-
dc.identifier.isiWOS:000373854600004-
dc.identifier.issnl1535-6108-

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