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by lentiviral and genome editing (e.g. CRISPR) methods Conduct qualitative and advanced quantitative fluorescence microscopy analyses Isolate proteins and assemblies from cancer cells for proteomic
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-Microscopy, in particular high-throughput approaches In vivo / ex vivo approaches: -Cognitive behavioral testing in mice (Y-maze, Barnes maze, EPM) -Analysis and interpretation of behavioral data
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, neurodegeneration, advanced microscopy, stem cell biology, and cell biology. The project will leverage state-of-the-art imaging facilities and established human iPSC-derived models of Alzheimer's disease. The work is
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operando monitoring of solid/solution interfaces. This will be done using advanced characterization techniques such as environmental scanning electron microscopy (ESEM), atomic force microscopy (AFM), Raman
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-paracrystalline (SPC) microstructure and the nanomorphology of donor-acceptor (BHJ) blends using techniques such as GISAXS and transmission electron microscopy (TEM) (Task 3.1). • Evaluation of the degradation and
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of animal material (e.g., electron microscopy, molecular analyses, in-vitro cell and tissue cultures, NGS sequencing); • experience in obtaining funding (e.g., grants from the National Science Centre
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of donor-acceptor (BHJ) blends using techniques such as GISAXS and transmission electron microscopy (TEM) (Task 3.1). • Evaluation of the degradation and aging of simple OSC devices, correlating the temporal
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our research program, see https://meyer-lab-cshl.github.io/ Position Responsibilities The successful candidate will study tolerance induction and generation of diversity in the immune system as part of
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responsible for studying neuronal swelling and dysfunction after excitotoxic injury, using advanced imaging techniques (including 2-photon microscopy) and electrophysiology. The position is within the Stead