D
David W. Dales
Researcher at London Health Sciences Centre
Publications - 10
Citations - 743
David W. Dales is an academic researcher from London Health Sciences Centre. The author has contributed to research in topics: Metastasis & Cell culture. The author has an hindex of 10, co-authored 10 publications receiving 725 citations. Previous affiliations of David W. Dales include University of Western Ontario & Lawson Health Research Institute.
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Journal ArticleDOI
Correction: Corrigendum: Stage of Breast Cancer Progression Influences Cellular Response to Activation of the WNT/Planar Cell Polarity Pathway
Connor D. MacMillan,Hon S. Leong,David W. Dales,Amy E. Robertson,John D. Lewis,Ann F. Chambers,Alan B. Tuck +6 more
TL;DR: Evidence is provided that PCP signaling can act in a context dependent manner to promote breast cancer progression and is expressed highest in 21MT-1 cells (invasive mammary carcinoma) and lowest in 21PT and 21NT cells.
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Crystal structure of human sex hormone-binding globulin: steroid transport by a laminin G-like domain.
Irina Grishkovskaya,George V. Avvakumov,Gisela Sklenar,David W. Dales,Geoffrey L. Hammond,Yves A. Muller +5 more
TL;DR: The crystal structure of the N‐terminal G domain of SHBG in complex with 5α‐dihydrotestosterone at 1.55 Å resolution reveals both the architecture of the steroid‐binding site and the quaternary structure ofThe dimer, and shows that G domains have jellyroll topology and are structurally related to pentraxin.
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Cloning of an ovine 11 beta-hydroxysteroid dehydrogenase complementary deoxyribonucleic acid: tissue and temporal distribution of its messenger ribonucleic acid during fetal and neonatal development.
TL;DR: Results demonstrate that 11 beta-HSD gene expression in sheep is regulated in a tissue-specific and developmentally programmed manner.
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Downregulation of osteopontin contributes to metastasis suppression by breast cancer metastasis suppressor 1.
Benjamin D. Hedley,Danny R. Welch,Alison L. Allan,Alison L. Allan,Waleed Al-Katib,David W. Dales,Carl O. Postenka,Graham Casey,Ian C. MacDonald,Ann F. Chambers +9 more
TL;DR: This study tested the hypothesis that re‐expression of OPN in metastasis‐suppressed 435/BRMS1 cells would reverse metastasis suppression and confer protection from stress‐induced apoptosis, and suggested that OPN downregulation by BRMS1 may be responsible, at least in part, for BR MS1‐mediated metastasis suppressed by sensitizing cancer cells to stress induced apoptosis.
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BRMS1 suppresses breast cancer metastasis in multiple experimental models of metastasis by reducing solitary cell survival and inhibiting growth initiation
Benjamin D. Hedley,Benjamin D. Hedley,Kedar S. Vaidya,Pushar Phadke,Lisa Mackenzie,David W. Dales,Carl O. Postenka,Ian C. MacDonald,Ann F. Chambers,Ann F. Chambers +9 more
TL;DR: Novel findings demonstrate that BR MS1 is a potent suppressor of metastasis in multiple organs, and identify two steps in the metastatic process that are sensitive to inhibition by BRMS1.