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The University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | 1 day ago
formulations and prototypes, conducting in vitro cell culture assays, and evaluating therapeutic performance in relevant mouse models. The researcher will contribute to experimental design, data analysis, and
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. Record of peer-reviewed publications in relevant scientific journals. Knowledge of adrenal gland biology, adrenal pathology, steroidogenesis, and cell differentiation/proliferation would be highly
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bacteria. This is a collaborative project with the Mager Lab (immunology). You can find more information about our group at https://www.linkmetabolism.com . Your tasks: Construction and screening of CRISPR
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Appointment Term: 1-2 years, renewable Appointment Start Date: Negotiable Group or Departmental Website: https://profiles.stanford.edu/alisamueller (link is external) How to Submit Application Materials: Please
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flow injection of water-based slugs into a push solvent followed by NMR detection of metabolites[1] . This platform included automated sample handling robotics, a custom-built flow cell, and precise
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: Immediately available Group or Departmental Website: https://med.stanford.edu/ophthalmology.html (link is external) How to Submit Application Materials: Please send application materials to Dr. Ahmad Al
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influence neurological diseases. Our research focuses on how transcription regulators mediate immune and brain cell behavior in both healthy and diseased states. We utilize a variety of techniques, including
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The LIT - Leibniz Institute for Immunotherapy (foundation under civil law) (https://lit.eu/ ) formerly RCI – is a biomedical research center focusing on translational immunology in the fields
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. Through integrated approaches combining molecular biology, transcriptomics, and functional assays in cellular models, the factors involved in bile flow dysfunction and the progression of liver damage will
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specific emphasis on the MR1/MAIT cell axis and its role in Alzheimer’s disease. Recent work from the group has demonstrated MR1-mediated antigen presentation by microglia, astrocytes and neurons, and