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Steffen Graether

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The main goal of our research program is to understand how the intrinsically disordered late embryogenesis abundant (LEA) proteins are able to protect plants from damage caused by cold, drought and high salinity. Our main focus has been on dehydrins, a group of abiotic stress response proteins that have been shown to protect plants from damage caused by drought and cold. Dehydrins are interesting in that they are composed of a variable number of conserved motifs that appear to have roles in protection of proteins, membranes and DNA from abiotic damage, as well as roles in localization.

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Philip Millar

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The primary aim of my research is to better understand the mechanisms that control, and functional consequences of, sympathetic outflow at rest and during stress in humans with and without cardiovascular disease. To uncover these mechanisms, my laboratory employs direct intra-neural recordings of postganglionic sympathetic traffic, studying both multi- and single-fibre preparations. Additionally, we are also interested in understanding the mechanisms responsible for the large inter-individual variability in blood pressure responses to stress, as well as testing novel interventions to reduce resting blood pressure, a major modifiable risk factor for cardiovascular disease.

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Georgina Cox

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The Cox lab aims to gain a better understanding of the molecular underpinnings of resistance mechanisms. Specifically, we study bacterial efflux systems, which will provide insight into their physiological functions and origins and will also support future drug discovery efforts and antibiotic stewardship. In addition, recognizing the need for innovation in the search for new antibacterial agents, we are exploring novel approaches to control bacterial infections by investigating the inhibition of bacterial adhesion to host cells.

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Kevin McCann

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Generally speaking, we are interested in understanding how biological structure, broadly defined to include structure of all biological forms, mitigates the stability and functioning of ecosystems. This question naturally leads to understanding how human impacts alter biological structure and so also how impacts may potentially alter the stability and functioning of whole ecosystems. This latter aspect of human impacts brings has our empirically motivated interests in developing practical biomonitoring techniques that span the ecological hierarchy. Our work is theoretical, empirical and experimental, and most often in aquatic ecosystems like streams, lakes and coastal oceans. We are highly collaborative and have worked globally on different ecosystems.

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Frederic Laberge

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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.

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