I study the neurophysiology of cognitive processes. My research focuses on eye movements and how they interact with cognitive and executive functions. For example, I explore how features are integrated across multiple brain areas to form object representations, how attention and object representations drive eye movements, and how the visual system prioritizes peripersonal space. I am also interested in the networks in the brain that perform all these processes and how they can be impaired due to concussion and subconcussive impacts.Learn More
Research Area: Neuroscience
My current research blends my research backgrounds in biomechanics and visuomotor control to examine how postural control is integrated and coordinated with voluntary movement (e.g. reaching, stepping, whole-body reaching). I am interested in developing an understanding of balance and movement both from a fundamental level, and in application to the immense problem of impaired mobility and falls in older adults and other clinical populations (e.g. stroke).Learn More
To date, my research program has focused on strategies used to execute safe movement during adapted locomotor tasks (steering, obstacle circumvention, obstacle stepping) and the role of vision in these tasks. I am also interested in exploring the impact of cognitive or brain function on locomotor control. Given the commonness of dual tasking in our daily living, I hope to map patterns of cognitive-locomotor interference for multiple adapted locomotor (e.g. obstacle circumvention) and cognitive activities (e.g. visuo-spatial cognitive tasks) and ascertain optimal training strategies for dual-task performance.Learn More
My research focuses on asymmetric RNA localization and localized translational control in animal species. I have also studied asymmetric RNA localization in neural stem cells and their contribution to both cellular differentiation and cortical development across species. Currently, my students and I are investigating various proteins that we think are important for RNA regulation during brain development.Learn More
The primary goals of my research program are 1) to understand where posture is controlled 2) to understand what sensory information contributes to successful movement and equilibrium.
By investigating these two key questions I believe we will have a better understanding of how sensory decline contributes to a loss of mobility as we age. My research program involves two key areas of study:
1) To perform direct recordings from sensory afferents and motor efferents in awake human subjects to investigate sensory contributions to movement, balance control, and reflex responses.
2) To elicit balance perturbations to test the function of these reflex loops, and sensory contributions to the maintenance of equilibrium and postural control.
Our research is focused on identifying and understanding the pathways by which environmental and social stressors are perceived, processed, and transduced into a neuroendocrine response. Several projects are aimed at elucidating how the neuroendocrine system orchestrates the stress response and focused specifically on the physiological functions of the corticotropin-releasing factor (CRF) system. Another major focus of the lab is to investigate the interactions between the neuroendocrine pathways that regulate the stress response and those involved in the regulation of appetite and growth.Learn More
My lab focuses on two main axes of research:
1) Unfolded Protein Response and Human Diseases: We study proteins that play key roles in animal stress responses, specifically the Unfolded Protein Response (UPR), which has been linked to animal development, cell differentiation, as well as a variety of human diseases such as Alzheimer’s, diabetes, cancer and viral infection.
2) Molecular Mechanisms of Aging: We are working to establish planarians as a new aging model to test the hypothesis that longevity requires multiplex resistance to stress. We hope to identify genes or alleles that confer such multiplex stress resistance and/or promote longevity.
In one main component, my students examine changes in the biodiversity of stream fishes caused by in-stream barriers used to control sea lamprey in the Laurentian Great Lakes. In a second main component, my students use smaller scale approaches focused on diversification in the foraging and migratory movements of brook charr (Salvelinus fontinalis) to understand the role that individual differences in behaviour have in facilitating population divergence in physiology, morphology, and life history, and the creation of new biodiversity. My research program has two, additional minor components: 1) assessing the effects of agricultural practices on stream fishes and 2) examining basic research questions related to animal movement.Learn More
We study proximate and ultimate questions around stress ecophysiology. We combine field studies and laboratory analyses to examine the persistent effects of early life stress on physiology, behaviour and fitness. We use a variety of approaches from large-scale manipulations in the wild to controlled laboratory experiments. I am excited by integrative questions that span levels of biological organization and students in the lab are encouraged to explore questions from evolutionary, ecological, physiological and molecular perspectives.Learn More
Research in our laboratory is focused on defining eukaryotic signal transduction pathways, and investigating how mutations in components of these pathways can contribute to human disease. Signal transduction is a central process in multicellular organisms that allows for the exchange of informational cues between and within cells. Current areas of research include: 1) Signalling pathways controlling kidney podocyte morphology; 2) focal adhesion dynamics in cancer cells; and, 3) characterization of a novel neuronal adaptor protein, ShcD.Learn More
While animal models have lead to huge advancements in our understanding of neurobiology, there is controversy over whether overexpression/silencing of gene expression is representative of diverse disease states. Indeed, the lack of availability of primary human neurons has made evaluating the pathological consequences of genomic mutations arduous. The use of human induced pluripotent stem cell (hiPSC) technology overcomes these limitations by providing a source of human neurons from both normal and disease genetic backgrounds. We currently focus on stem cell based models of Parkinson's Disease (PD) to study how mitochondrial stress mechanisms impact on neuronal function in human disease.Learn More
The Sanders lab is interested in how neurons use the protein-lipid modification palmitoylation to target proteins to subcellular locations and to define how palmitoylation-dependent targeting contributes to physiological neuronal function and neuropathological conditions. Current projects include characterizing how palmitoylation of vesicular transport machinery regulates fast axonal transport and how palmitoylation of ion channels and their scaffold proteins regulates clustering at the axon initial segment, a critical site of neuronal excitability where action potentials are generated.Learn More
Current projects include:
- Mechanistic and functional connections between stress and adult neurogenesis in fish
- Effects of aquatic pollutants on fish physiology, morphology, and performance
- Neuroanatomy and regenerative capacity of the hagfish brain
- Quantitative proteomics as a tool for biomarker discovery and novel insights into animal physiology
My research program adopts a broad and integrative approach to the study of chronic musculoskeletal pain, incorporating both basic and clinical sciences. A major arm to my research program is investigating the underlying pathophysiologic mechanisms using both animal and human models. My research also aims to advance reliable diagnostic criteria (imaging, biomarkers) and physical assessment techniques (quantitative sensory testing, electromyography) that enable effective and reliable treatment and management strategies. By emphasizing transdisciplinary and multi-institutional collaborations, my research program will continue to inform future clinical and experimental initiatives in the field of chronic musculoskeletal pain.Learn More
The growth of neurons and their organization into circuits is a tightly controlled process that follows a series of well-defined steps. Once differentiated and integrated into networks, neurons also retain a remarkable capacity to rapidly change the arrangement of their connections in response to activity, a feature that is believed to critically support cognition as well as our ability to learn and retain information for long periods of time. Accumulating evidence strongly suggests that perturbation of the molecular interactions responsible for the growth of neurons, or the capacity of these cells to adequately respond to activity-dependent signals, contributes to the pathophysiology of different brain disorders. Our laboratory uses a multidisciplinary approach to explore these questions.Learn More
Currently, there are several major areas of research focus including the study of basic fatty acid metabolism, understanding the association between plasma fatty acids and health outcomes, omega-3 fatty acids in the prevention of breast cancer, and examining determinants of health in the Guelph Family Health Study. In addition, related projects include the study of fats in brain health (concussion, Alzheimer's Disease), fatty liver disease, fatty acid metabolism, bone development and nutrigenomics.Learn More
Dr. Heyland's laboratory uses novel functional genomics approaches to study the endocrine and neuroendocrine systems of aquatic invertebrates. Specifically he investigates the function and evolution of hormonal and neurotransmitter signaling systems in the regulation of development and metamorphosis. His research includes evolutionary development studies of marine invertebrate metamorphosis, eco-toxicogenomic approached to understand endocrine disruption in aquatic ecosystems and water remediation technologies. These projects are integrated with several national and international collaborations ranging form basic scientific work to industry partnerships.Learn More
Our research typically involves assessing animals' preferences for and responses to 'enriched' housing conditions that are more complex and naturalistic than the standard norms; investigating abnormal behaviours like stereotypic pacing; validating potential welfare indicators (e.g. facial expressions), and we also analyse multi-species datasets to looks for species-level welfare risk and protective factors. We have worked or are working with mink, rats, mice, rhesus monkeys and zebra fish; and with large datasets from elephants, Carnivora, parrots and lemurs.Learn More
Work in the Laberge lab attempts to understand how variation in brain structure and size influences organismic function, and identify the factors that drive evolution and plasticity of the nervous system. Current projects on this topic study variation in structure and size of the brain in populations of fish and amphibians, the proximate mechanisms generating this variation, and the functional consequences of this variation. Additionally, the lab is involved in collaborative efforts aiming to develop novel indicators of ecological performance and chronic stress in wild fish.Learn More