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-clamp electrophysiology, quantitative imaging, protein engineering, structural methods (cryo-EM, X-ray, MD modeling), lipid biochemistry, and/or disease models (rodents or organoid/organ-on-chip). Duke
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) and their relationships with neighboring tissues in pathophysiological conditions. We utilize in vivo mouse genetics, live imaging, 3D organoids, genome-wide Cas9/Crispr based functional genetic
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