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to establish foundational models to predict the effects of potential drug candidates on cardiovascular diseases. By combining genome engineering, functional genomics, and tissue models, we aim to advance
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researcher to work on Cellular Regulation and Mechanisms of Protein Arginylation Modification. Our research is aiming to elucidate the biological functions of arginylation, discover the protein substrates
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offers the opportunity to work on translational models, cutting-edge omics technologies, and contribute to high-impact publications in a collaborative research environment. Job Description Primary Duties
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hematopoietic stem and multipotent progenitor populations to modulate lineage output for therapeutic purpose in diseases and aging context. This project will involve primary mouse and human stem cell sorting
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. Mellon Foundation, DSISS is starting a new phase of translational work to advance practical and technical solutions for integrating CARE into professional practice and infrastructure, with a focus on
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, as well as clinical medicine, work together to both computationally design and experimentally characterize novel biomolecules. Current projects include the design of novel therapeutics for cancer
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system. This role would advance three, ongoing NIH/NIA R01 funded grants that investigate the long-term impact of AD brain pathology on driving behavior and driving cessation among persons with and without
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candidate will investigate the functions of bile metabolites induced by bacterial infection. We aim to advance our understanding of how infection-stimulated bile metabolites influence intestinal defense
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processing of social information in patients with psychiatric conditions remain largely unclear. We use a suite of cutting-edge techniques, including in vivo multi-photon imaging, fiber photometry, and custom
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Position Summary Candidate will conduct full-time research on topics including novel histone modifications (epigenetic marks) and their role in immune regulation, cancer and metabolism. Job