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state-of-the-art magnetic resonance imaging (MRI) in parallel to behavioural assessment and histology. The overall goal of the project is to investigate the impact of radiotherapy in brain development
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to neurodegenerative disorders. Your PhD project specifically will focus on developing and applying a versatile high-throughput fluorescence imaging platform. In this function you will: optically design a microscope
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X-ray videocystometry in awake mice. The candidate will design and conduct experiments exploring the signalling interactions between urothelial cells and sensory nerves innervating the bladder, and
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advanced techniques such as ex vivo calcium imaging and transcriptomics of mouse and human urothelium and DRG neurons, and X-ray videocystometry in awake mice. The candidate will design and conduct
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their evolution during catalytic operation and activation. You will apply advanced electron diffraction techniques (3DED, 4D-STEM tomography), atomic resolution STEM imaging (HAADF, ABF), EDX and EELS
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characterized ex situ by electron microscopy and x-ray photoelectron spectroscopy, and under operating conditions by X-ray absorption spectroscopy (XANES and EXAFS) and high-resolution Raman and diffuse
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nanotubes. The most efficient catalysts will be characterized ex situ by electron microscopy and x-ray photoelectron spectroscopy, and under operating conditions by X-ray absorption spectroscopy (XANES and
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. This is still a very new research topic and many scientific questions remain unanswered. Alongside the modelling research, there will also be a measurement campaign using high-speed imaging and in-line
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highly motivated by applied research involving conceptual evaluation as well as experimental evaluation by means of prototype implementations, able to work well in a diverse group, comfortable giving and
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the genetic and clinical variability of PRPH2-IRD by studying a large patient cohort with detailed genetic analysis and advanced imaging techniques. The project will focus on identifying genotype–phenotype