Faculty Members Currently Qualified to Supervise Graduate Students
      
          ![]() Dr. Kristi Baker  | 
          Our lab studies differences in how the specialized mucosal immune in the intestine sees tumors with different patterns of genomic instability and how this translates into different forms of anti-tumor immune responses.
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          ![]() Dr. Vickie Baracos  | 
          Metabolism in 
                        wasting disorders: skeletal muscle atrophy and 
                        cancer-associated cachexia. A number of pathological 
                        states may be defined as wasting disorders - several 
                        examples include cancer, AIDS, chronic obstructive 
                        pulmonary disease. My research program focuses on the 
                        metabolic abnormalities that underlie this wasting, 
                        particularly of the skeletal muscles.
                        More... | 
        
![]() Dr. Gordon Chan  | 
           In my laboratory, research is centered on the mechanism 
                        of cell cycle control and particularly the regulation of 
                        accurate, chromosome segregation during mitosis. The 
                        mitotic checkpoint is a failsafe mechanism by which the 
                        cell prevents premature anaphase and ensures accurate 
                        chromosome segregation.  By investigating the 
                        molecular mechanism of the mitotic checkpoint, we can 
                        better evaluate these genes as potential cancer drug 
                        targets as well as contributing to the basic 
                        understanding of cancer.More | 
        
![]() Dr. Yangxin Fu  | 
            The objective of the Fu laboratory is to better understand the molecular mechanisms underlying ovarian tumorigenesis, with a particular interest in the role of Notch signaling pathway in ovarian cancer development and progression. More... 
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![]() Dr. Armin Gamper  | 
           My research examines how cells respond to genotoxic stress, how aberrant regulation of these response pathways affects tumorigenesis and how the DNA damage response can be targeted by drugs to improve radiation or chemotherapy. By studying the influence of genetic factors on the DNA damage response, I hope to discover diagnostic and predictive biomarkers that can be applied for personalized medicine. My approach integrates protein chemistry, proteomics, reverse chemical genetics, molecular and cell biological methods, and animal models. 
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![]() Dr. Roseline Godbout  | 
           Retinoblastoma, a childhood tumour of the retina, 
                        results from malignant transformation of precursor 
                        cells. Retinal precursors are multipotent 
                        neuroectodermal cells that can differentiate into all 
                        the different types of neuronal and glial cells that 
                        make up the mature tissue. There are  currently two major projects in the lab. The first is to study the function and regulation of genes that are expressed at the early stages of retinal development. The second is to study the role of the DEAD box gene DDX1, encoding an RNA unwinding protein, in normal retinal development and in retinoblastoma. More...  | 
        
![]() Dr. Michael Hendzel  | 
          In my laboratory, we are examining how chromatin and 
                        regulatory molecules are compartmentalized within the 
                        cell nucleus. Our current research programs involve 
                        defining the dynamics of movement of chromatin, 
                        subnuclear structures involved in compartmentalizing 
                        regulatory molecules that act on chromatin and RNA, and 
                        the movement of individual regulatory molecules within 
                        the cell nucleus. We have found that most molecules move 
                        considerably slower than expected for their molecular 
                        weight. More... | 
        
![]() Dr. Ismail Ismail  | 
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![]() Dr. Mary Hitt  | 
           My research focuses on the development of gene therapy  
                        vectors that minimize these side effects without 
                        compromising anticancer activity. Currently we are 
                        investigating adenovirus vectors carrying modified fiber 
                        proteins and/or tissue-specific promoters to target 
                        expression of toxic genes specifically to the tumor.
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![]() Dr. John Lewis 
  | 
           We study prostate cancer, the most commonly diagnosed cancer in Canadian men. Our goal is to foster an environment where scientists, doctors and clinical researchers work together to address key challenges in prostate cancer care. As a team, we hope to accelerate the transfer of research discoveries from the "bench to the bedside" to make an impact on those living with cancer.  More...  | 
        
![]() Dr. David Murray  | 
          The basic research in my 
                        laboratory focuses on understanding the basic
                        mechanisms by which mammalian cells respond to ionizing 
                        radiation and
                        DNA-damaging anticancer drugs, with an emphasis on 
                        DNA-repair pathways. My major
                        area of translational research interest is in 
                        identifying the genetic factors
                        (polymorphisms) that determine the extreme response of 
                        some cancer patients to
                        anticancer therapeutics such as radiation therapy and 
                        cisplatin-based
                        chemotherapy.
                        More...
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![]() Dr. Lynne-Marie Postovit  | 
          One of our major goals is to see the work that we do in the lab translate into new treatments or early detection methods for cancer patients:  We want to translate our scientific results into clinical practice. 
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![]() Dr.Alan Underhill  | 
          The Underhill laboratory is interested in 
deciphering how master regulators of melanocyte development contribute to 
melanoma pathogenesis. In addition, we are also examining how histone 
modifications regulate the balance between cell proliferation and 
differentiation, and how this is overridden in cancer..
More.... 
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![]() Dr. Michael Weinfeld  | 
          Several years ago we 
                        developed a postlabelling assay that allowed us to 
                        detect a number of lesions in irradiated DNA. We have 
                        applied this assay to the study of drugs that enhance 
                        the level of DNA damage in radioresistant and 
                        chemotherapy-resistant hypoxic cells. We observed that 
                        these drugs can mimic oxygen by producing DNA strand 
                        breaks with specific termini that require additional 
                        processing before the strands can be rejoined. We have 
                        also made use of the assay to monitor the repair of 
                        these lesions by purified enzymes and cell-free 
                        extracts.
                        More.... | 
        
![]() Dr. Frank Wuest  | 
          My research is embedded in the multidisciplinary field of translational cancer research. Research efforts are mainly aimed at the evaluation and translation of the diagnostic and therapeutic potential of novel molecular targets involved in the development and progression of cancer by means of molecular imaging techniques to enhance patient care. 
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