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molecular biology and ideally with proven track record in the fields of biomedical research, rare diseases or vascular/lymphovascular sciences. Post-doc experience preferentially in the fields of lympho
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Activities: Research Topic: Alveolar injury and repair in Pompe disease. Job Description: Pompe disease (PD), is a rare autosomal recessive disorder caused by a deficiency of acid alpha-glucosidase (GAA) – a
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therapeutic strategy using genetically engineered MSCs to provide novel treatment options for two rare ocular surface diseases leading progressively to blindness. The project is funded by AFM-Téléthon and
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position within a Research Infrastructure? No Offer Description One post-doctoral position is available within the scope of the project “Modeling of monogenic diseases for pathophysiological studies and
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researcher to investigate iron homeostasis in rare human diseases, focusing on how cellular iron levels impact metabolic functions and contribute to disease pathologies. Additionally, the research will involve
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The Department of Biomedicine (DBM) integrates basic and clinical researchers from University of Basel and University Hospitals committed to deepen the understanding of health and disease while
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Post-doctoral Fellow in the Department of Orthopaedics and Traumatology, School of Clinical Medicine
talented Post-doctoral Fellow to join our multidisciplinary research team focusing on the molecular mechanisms of musculoskeletal diseases, including intervertebral disc degeneration (IVDD) and rare bone
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-sustainable incumbents in light-emitting applications, such as rare-earth-based phosphors and heavy-metal-based quantum dots. We will explore the potential of these sustainable luminescent nanomaterials as
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applicants for a 12-month, 100%-time postdoctoral associate. This position is intended for candidates with strong training in quantitative epidemiology, data analysis, and population-level disease research
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Post-doctoral Fellow in the Department of Orthopaedics and Traumatology, School of Clinical Medicine
diseases, including intervertebral disc degeneration (IVDD) and rare bone diseases like Pseudoachondroplasia (PSACH). Given that skeletal disorders often involve complex "ER storage" pathologies and genetic