PKA signaling drives mammary tumorigenesis through Src.

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Bibliographic Details
Title: PKA signaling drives mammary tumorigenesis through Src.
Authors: Beristain AG; Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada., Molyneux SD; 1] Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada [2] Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada., Joshi PA; 1] Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada [2] Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada., Pomroy NC; Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada., Di Grappa MA; Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada., Chang MC; Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada., Kirschner LS; Division of Endocrinology, Diabetes and Metabolism, The Ohio State University, Columbus, OH, USA., Privé GG; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada., Pujana MA; Breast Cancer and Systems Biology Unit, Translational Research Laboratory, Catalan Institute of Oncology, IDIBELL, L'Hospitalet del Llobregat, Barcelona, Spain., Khokha R; 1] Ontario Cancer Institute, Princess Margaret Hospital, Toronto, Ontario, Canada [2] Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada [3] Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, Ontario, Canada.
Source: Oncogene [Oncogene] 2015 Feb 26; Vol. 34 (9), pp. 1160-73. Date of Electronic Publication: 2014 Mar 24.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 8711562 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5594 (Electronic) Linking ISSN: 09509232 NLM ISO Abbreviation: Oncogene Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1476-5594
DOI:10.1038/onc.2014.41