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Field
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preconception environmental exposures in animal models. Contribute to research projects investigating seminal plasma metabolomics, sperm mitochondrial biomarkers, and related mechanisms influencing reproductive
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waveguides (such as photonic crystal fibres and capillaries) filled with gases, liquids, and plasmas. We use these light sources for both fundamental science (such as the physics of nonlinear optics, ultrafast
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of Ageing, the CZI and ongoing collaboration with the pharma industry. Our current research projects include the analysis of: • Plasma, CSF and Brain Proteomic analysis • Biomarker identification through
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. Extensive hands-on experience with analytical characterization of bioprocess samples, including high-performance liquid chromatography (HPLC), gas chromatography (GC), inductively coupled plasma optical
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diagnostic techniques such as infrared imaging and spectroscopy, thermal imaging, Raman spectroscopy for metals and ceramics, plasma emission spectroscopy, non-destructive ultrasonic spectroscopy and testing
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-of-the-art facilities, explore fundamental plasma dynamics and non-equilibrium plasma chemistry inherent to air-breathing thrusters, and assess propulsion performance using industry-standard thrust stands
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website: https://cruchagalab.wustl.edu/ . Research Projects: Plasma, CSF and Brain Proteomic analysis. Biomarker identification through the use of machine learning and AI approaches. Integration
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of metallic/alloy powders, AM of metals and/or other powderbased manufacturing technologies such as hot isostatic pressing or spark plasma sintering of alloys/composites, alloy development including a strong
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staining, Golgi staining, and use of fluorescent probes to interrogate cellular and subcellular mechanisms. Apply advanced subcellular fractionation workflows to isolate mitochondria, ER, MAM, plasma
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University of North Carolina at Chapel Hill | Chapel Hill, North Carolina | United States | about 2 months ago
); fibrin(ogen) degradation and the cellular and enzymatic drivers of thrombus resolution beyond plasminogen; and cellular and plasma mediators of FXI biology that influence bleeding risk. Additional