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to elucidate cellular and molecular mechanisms underlying DMD and healthy aging, employing iPSC-derived cellular models, skeletal muscle differentiation, and three-dimensional muscle tissue engineering
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genetics and cell biology applied to Duchenne Muscular Dystrophy (DMD) and aging, using induced pluripotent stem cells (iPSCs). The project aims to elucidate cellular and molecular mechanisms underlying DMD
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, with a view to circular economy. The scholarship recipient will be responsible for further investigating the interaction mechanisms involved during the sorption and desorption process, evaluating
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collisions applied to Large Hadron Collider (LHC) and/or the Electron-Ion Collider (EIC) and experimental data analysis with ALICE (A Large Ion Collider Experiment) or Stellar Intensity Interferometry (SII) in
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secretion system (T6SS) found in bacteria of the Xanthomonaceae family. For that, a combination of biochemical and structural biology techniques will be employed to dissect the mechanisms of recruitment
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such as cryo-electron microscopy, omics analyses, synchrotron light, and computational approaches. Responsibilities include integrating experimental and theoretical results, contributing to scientific
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monitoring, dental hydraulic conductance, animal experimentation, and pulp response in rats. Applications must be sent by e-mail to André Luiz Fraga Briso (andre.briso@unesp.br ), the project's Co-PI, between
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on subcellular Ca2+ oscillations and their impact on genomic integrity and on the recruitment of different DNA repair mechanisms. Candidates must have a proven track record of scientific achievements in post