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BMC Cancer|November 5, 2011
GnRH receptor activation competes at a low level with growth signaling in stably transfected human breast cell linesKevin Morgan, Colette Meyer, Nicola Miller, et al.
BMC Medical Genomics|September 23, 2008
The removal of multiplicative, systematic bias allows integration of breast cancer gene expression datasets - improving meta-analysis and prediction of prognosisAndrew H Sims, Graeme J Smethurst, Yvonne Hey, et al.
Genome Biology|October 5, 2012
Tissue of origin determines cancer-associated CpG island promoter hypermethylation patternsDuncan Sproul, Robert R Kitchen, Colm E Nestor, et al.
Cells|March 8, 2020
The G Protein-Coupled Estrogen Receptor (GPER) Expression Correlates with Pro-Metastatic Pathways in ER-Negative Breast Cancer: A Bioinformatics AnalysisMarianna Talia, Ernestina Marianna De Francesco, Damiano Cosimo Rigiracciolo, et al.
Oncotarget|May 27, 2015
Monocytes and macrophages, implications for breast cancer migration and stem cell-like activity and treatmentRebecca Ward, Andrew H Sims, Alexander Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2011
Transcriptionally repressed genes become aberrantly methylated and distinguish tumors of different lineages in breast cancerDuncan Sproul, Colm Nestor, Jayne Culley, et al.
Cancer Research|August 8, 2014
Molecular changes in lobular breast cancers in response to endocrine therapyLaura M Arthur, Arran K Turnbull, Victoria L Webber, et al.
Cancer Letters|February 22, 2019
Pharmacological inhibition of the IKKε/TBK-1 axis potentiates the anti-tumour and anti-metastatic effects of Docetaxel in mouse models of breast cancerRyan T Bishop, Silvia Marino, Daniëlle de Ridder, et al.
Oncogene|December 17, 2021
Elevated EDAR signalling promotes mammary gland tumourigenesis with squamous metaplasiaRebecca Williams, Stephanie Jobling, Andrew H Sims, et al.
Cancers|October 3, 2020
Functional Transcription Factor Target Networks Illuminate Control of Epithelial RemodellingIan M Overton, Andrew H Sims, Jeremy A Owen, et al.
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