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Terry Fox Laboratory - BC Cancer Agency

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Biennial Research Report 2005 ‐200639. Role of DNA methylation in controlling syncytin: a novel gene implicated in multiple sclerosisPI: D MagerMultiple Sclerosis Society$35,000 (2005)$35,000 (2006)$70,000 (2005‐2006)40. Role of LFA‐1 in cell mediated cytotoxicityPI: F TakeiCIHR$58,632 (2005)$58,632 (2006)$586,315 (2005‐2010)41. Role of RasGRP1 in <strong>BC</strong>R‐induced deletion of immature B cellsPI: R KayCIHR$117,336 (2005)$117,336 (2006)$821,347 (2004‐2008)This project will investigate if the ERV transcriptional promoter ofthe syncytin gene is a sensitive target for epigenetic regulation andthat perturbations in this regulation may be involved in multiplesclerosis.The goal of this study is to understand how a protein called LFA‐1involved in cell‐cell binding acts to initiate the cascade of events toguide ‘killer lymphoctye’ cells of the immune system to attackdiseased cells.The goal is to understand the molecular mechanism by which RasGRP1 increases the sensitivity of immature B cells to survivalsignal suppression and induction of cell death. Insight intoregulation of B cell activation vs. deletion is critical to ensureeffective immune response to foreign antigens while avoidingauto‐immunity.TERRY FOX LABORATORY42. Role of retroelements in age related gene expressionPI: D MagerCIHR (Pilot Project)$49,942 (2005)$49,942 (2006)$100,000 (2006‐2007)43. Stem cell and gene regulationPI: A EavesCo‐PIs: C Eaves, D Hogge, PHoodless, K Humphries, RKay, G Krystal, P Lansdorp, DMager, C Smith, HSutherland, F TakeiMSFHR Research Unit$250,000 (2005)$250,000 (2006)$1,000,000 (2003‐2008)44. Stem cell centrePI: P LansdorpCFI$1,008,384 (2005)$1,008,384 (2006)$3,775,195 (2002‐2005)45. Stem cell centre ‐ infrastructure operating fundsPI: P LansdorpCFI$110,079 / yr (2005, 2006)$231,346 (2003‐2006)This project will investigate whether the gradual, age‐relateddemethylation of retroelements, located within or near genes canlead to altered expression of genes.This goal is to enhance studies to understand the molecularpathways that govern stem cell renewal, viability, theirdevelopment into specific types of cells, their ability to multiplyand their genome stability.This project will address new questions in stem cell biology andexplore emerging possibilities for the use of stem cells inregenerative medicine. The centre will comprise of threelaboratories: a stem cell sorting and analysis laboratory, a genevector laboratory and a Good Manufacturing Practice (GMP) StemCell Processing <strong>Laboratory</strong>.Partial infrastructure operating funds for the stem cell centreproject.161

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