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signaling pathways that promote lung injury resolution. The studies will include using cell culture and organoid models to provide mechanistic insight of murine models of lung injury. We seek candidates with
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liver resection and transplant. We use multidisciplinary approaches including in vitro and in vivo models of I/R injury, biochemical and genetic analysis, transcriptomics, imaging with live cells and
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: Using biogeochemical evolutionary models to simulate lifeless and inhabited worlds, and Developing disequilibrium-, redox-, and information-based metrics to understand and quantify the influence of life
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models to simulate lifeless and inhabited worlds, and Developing disequilibrium-, redox-, and information-based metrics to understand and quantify the influence of life on planetary environments
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), positron emission tomography (PET), functional MRI (fMRI), electroencephalography (EEG), behavior, genetics, and proteomics using advanced quantitative modeling techniques and artificial intelligence
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: Using biogeochemical evolutionary models to simulate lifeless and inhabited worlds, and Developing disequilibrium-, redox-, and information-based metrics to understand and quantify the influence of life
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repair, oxidative stress, metabolic rewiring, and immune modulation in FLASH/UHDR-RT). Preclinical model development (orthotopic murine systems, patient-derived xenografts, 3D organoids). Correlative
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Position Summary Dr. Amargant-Riera’s research laboratory focuses on understanding the mechanisms that define oocyte quality. The lab uses mouse models and human samples to investigate
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would have the opportunity to work with colleagues working on animal models of streptococcal sepsis and IE. This project is a multi-PI collaborative project with Paul Sullam (Microbiologist at UCSF
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, tumor immunology organotypic in-vitro models, genetically engineered animal models and human tissues from clinical trials. All these approaches are brought to bear on impactful questions in tumor