Keith Bonham

Affiliations: 
University of Saskatchewan, Saskatoon, SK, Canada 
Area:
Biochemistry, Molecular Biology
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"Keith Bonham"
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Publications

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Kirzinger MWB, Vizeacoumar FS, Haave B, et al. (2019) Humanized yeast genetic interaction mapping predicts synthetic lethal interactions of FBXW7 in breast cancer. Bmc Medical Genomics. 12: 112
Parameswaran S, Vizeacoumar FS, Kalyanasundaram Bhanumathy K, et al. (2018) Molecular characterization of a MLL1 fusion and its role in chromosomal instability. Molecular Oncology
Ogunbolude Y, Dai C, Bagu ET, et al. (2017) FRK inhibits breast cancer cell migration and invasion by suppressing epithelial-mesenchymal transition. Oncotarget. 8: 113034-113065
Bagu ET, Miah S, Dai C, et al. (2017) Repression of Fyn-related kinase in breast cancer cells is associated with promoter site-specific CpG methylation. Oncotarget
Cunningham CE, Li S, Vizeacoumar FS, et al. (2016) Therapeutic relevance of the protein phosphatase 2A in cancer. Oncotarget
Miah S, Goel RK, Dai C, et al. (2014) BRK targets Dok1 for ubiquitin-mediated proteasomal degradation to promote cell proliferation and migration. Plos One. 9: e87684
Mellor P, Deibert L, Calvert B, et al. (2013) CREB3L1 is a metastasis suppressor that represses expression of genes regulating metastasis, invasion, and angiogenesis. Molecular and Cellular Biology. 33: 4985-95
Mellor P, Junek S, Just N, et al. (2011) Abstract 1450: Loss of the UPR member CREB3L1 is vital for the survival of breast cancer cells in the tumor microenvironment and development of the metastatic phenotype Cancer Research. 71: 1450-1450
Hirsch CL, Ellis DJ, Bonham K. (2010) Histone deacetylase inhibitors mediate post-transcriptional regulation of p21WAF1 through novel cis-acting elements in the 3' untranslated region. Biochemical and Biophysical Research Communications. 402: 687-92
Ellis DJ, Lawman ZK, Bonham K. (2008) Histone acetylation is not an accurate predictor of gene expression following treatment with histone deacetylase inhibitors. Biochemical and Biophysical Research Communications. 367: 656-62
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