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Field
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Hospital. The Han laboratory studies the biology of primary cilia and how cilia-dependent signaling regulates cell behavior in normal development and disease, with particular emphasis on brain development
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of the Bacterial Cell Wall Unit headed by Ivo G. Boneca. This is a collaborative project with the teams of Raquel Mejias-Luque of the Technical University of Munich and of Richard Ferrero of the Monash University
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and maximise data sharing within the Oxford–AbbVie initiative. It is essential that you hold a PhD/DPhil (or be close to completion) in immunology or a related area and demonstrate commitment to a team
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of the scientific career or a Post-Doc, with an interest to pursue scientific goals in the area of polymer chemistry and material chemistry by means of polymer synthesis, physicochemical characterization of polymeric
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University of North Carolina at Greensboro | Greensboro, Indiana | United States | about 3 hours ago
or Chemistry; fully trained and very experienced in cell culturing, biological sample preparation from cells and tissues; skilled in biological interpretation of research data in the context of disease mechanism
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electromagnetic shielding performance. Current focus areas include magnetic MXenes and large-unit-cell magnetic hexaferrites, although candidates with expertise in related aspects of computational materials
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also performs a number of molecular biology and immunologic techniques, including flow cytometry and other cell-based assays. The successful candidate will join a collaborative, multidisciplinary team
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the biology inside the chip. Using human bone explants and cells, you will optimise the BBoC model for studying bone remodelling, with a particular focus on osteoclasts and their interaction with osteoblasts
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mice -Xenotransplantation if human cells and PDX models -IP, SQ, and IV injection of cancer and immune cells -Bioluminescent imaging of mice -Caliper measurments and calculation of tumor volumes Routine
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orofacial cleft, in zebrafish and/or in tissue culture, · testing non-coding variants associated with orofacial cleft by engineering the genotype of human IPSCs and differentiating them into oral cell