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modeling. 80% research - The project focuses on developing theoretical models using optimization and information theory to improve understanding of plant hydraulic regulation at the leaf, plant, and
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, Molecular Biology, or a closely related biomedical field • Experience with retinal immunopathology, photoreceptor biology, or RPE-related degenerative disease models • Demonstrated expertise in retinal
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validate polarizable force field models. Responsibilities will include both macroscopic property analysis (e.g., density, diffusion coefficients, ion conductivity, interfacial tension) and atomistic-level
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-activated immunogenicity, scaled-up vector production, and assessment of AAV efficacy in pre-clinical animal models. The goal of our research is to ensure advancement of gene therapy treatment for patients
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tissue culture, experimental virology, transcriptome analyses, and immunologic assays. Prior experience conducting relevant experiments using in vitro and in vivo models of infection, such as flow
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of innovative models that simulate the intestinal environment and study disease progression. Participate in peer-reviewed manuscripts in top scientific journals and contribute to scientific grant funding
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) as models. PXR and CAR transcriptionally regulate cytochrome P450 3A4 (CYP3A4) and CYP3A5-drug-metabolizing enzymes that metabolize more than 50% of clinical drugs, the dysregulation of which
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induced pluripotent stem cells derived cardiac organoids for disease modeling and gene editing. This research aims to deepen our understanding of dystrophic cardiomyopathy and develop novel therapeutic
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with mouse models of neurodegenerative diseases, demyelinating conditions, and brain tumors • Expertise in flow cytometry, including high-dimensional (spectral) flow cytometry for immune phenotyping
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(Including histone modification and DNA methylation) and 3D genome organization studies on the interplay between EBV infection and host interactions. Using in vitro B cell transformation model and 3D organoid