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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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: 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
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(including Crohn’s disease and ulcerative colitis) using molecular and cell biology, multi-omics technologies, murine models, and human tissues. We currently have three major focuses: 1) Innate lymphoid cells
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experience in molecular and cellular neurobiology to study neuronal regeneration and preservation in retinal mouse models of injury and disease. This project will examine how cellular metabolism impacts