Institute of Cancer Sciences
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The mitogenic action of insulin-like growth factor I in normal human mammary epithelial cells requires the epidermal growth factor receptor tyrosine kinase.
The Journal of biological chemistry Jan, 2004 | Pubmed ID: 14593113
Isoindolinone-based inhibitors of the MDM2-p53 protein-protein interaction.
Bioorganic & medicinal chemistry letters Mar, 2005 | Pubmed ID: 15713419
Small-molecule inhibitors of the MDM2-p53 protein-protein interaction based on an isoindolinone scaffold.
Journal of medicinal chemistry Oct, 2006 | Pubmed ID: 17034127
Novel cell culture technique for primary ductal carcinoma in situ: role of Notch and epidermal growth factor receptor signaling pathways.
Journal of the National Cancer Institute Apr, 2007 | Pubmed ID: 17440163
Mammary stem cells and breast cancer--role of Notch signalling.
Stem cell reviews Jun, 2007 | Pubmed ID: 17873349
Prolactin receptor antagonism reduces the clonogenic capacity of breast cancer cells and potentiates doxorubicin and paclitaxel cytotoxicity.
Breast cancer research : BCR , 2008 | Pubmed ID: 18681966
Are stem-like cells responsible for resistance to therapy in breast cancer?
Breast disease , 2008 | Pubmed ID: 19029627
Resistance to endocrine therapy: are breast cancer stem cells the culprits?
Journal of mammary gland biology and neoplasia Mar, 2009 | Pubmed ID: 19252972
Regulation of breast cancer stem cell activity by signaling through the Notch4 receptor.
Cancer research Jan, 2010 | Pubmed ID: 20068161
Breast cancer stem cells: something out of notching?
Cancer research Nov, 2010 | Pubmed ID: 21045140
Breast cancer stem cells and their role in resistance to endocrine therapy.
Hormones & cancer Apr, 2011 | Pubmed ID: 21761332
P-Cadherin is Co-Expressed with Cd44 and Cd49f and Mediates Stem Cell Properties in Basal-Like Breast Cancer.
Stem cells (Dayton, Ohio) Mar, 2012 | Pubmed ID: 22389315
A detailed mammosphere assay protocol for the quantification of breast stem cell activity.
Journal of mammary gland biology and neoplasia Jun, 2012 | Pubmed ID: 22665270
Targeting CXCR1/2 significantly reduces breast cancer stem cell activity and increases the efficacy of inhibiting HER2 via HER2-dependent and -independent mechanisms.
Clinical cancer research : an official journal of the American Association for Cancer Research Feb, 2013 | Pubmed ID: 23149820
Combined inhibition of ErbB1/2 and Notch receptors effectively targets breast ductal carcinoma in situ (DCIS) stem/progenitor cell activity regardless of ErbB2 status.
PloS one , 2013 | Pubmed ID: 23457626
Recent advances reveal IL-8 signaling as a potential key to targeting breast cancer stem cells.
Breast cancer research : BCR , 2013 | Pubmed ID: 24041156
Lapatinib inhibits stem/progenitor proliferation in preclinical in vitro models of ductal carcinoma in situ (DCIS).
Cell cycle (Georgetown, Tex.) , 2014 | Pubmed ID: 24247151
A differential role for CXCR4 in the regulation of normal versus malignant breast stem cell activity.
Oncotarget Feb, 2014 | Pubmed ID: 24583601
Focal adhesion kinase and Wnt signaling regulate human ductal carcinoma in situ stem cell activity and response to radiotherapy.
Stem cells (Dayton, Ohio) Feb, 2015 | Pubmed ID: 25187396
Anti-estrogen Resistance in Human Breast Tumors Is Driven by JAG1-NOTCH4-Dependent Cancer Stem Cell Activity.
Cell reports Sep, 2015 | Pubmed ID: 26387946
High mitochondrial mass identifies a sub-population of stem-like cancer cells that are chemo-resistant.
Oncotarget Oct, 2015 | Pubmed ID: 26421710
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
The Journal of pathology Nov, 2016 | Pubmed ID: 27512948
Patient-derived Mammosphere and Xenograft Tumour Initiation Correlates with Progression to Metastasis.
Journal of mammary gland biology and neoplasia Dec, 2016 | Pubmed ID: 27680982
Erratum to: Patient-Derived Mammosphere and Xenograft Tumour Initiation Correlates with Progression to Metastasis.
Journal of mammary gland biology and neoplasia Dec, 2016 | Pubmed ID: 27815673
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