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on the supervisory groups emerging molecular insights into EIPH, the project will explore microvasulaturedysfunction in the initiation and progression of disease, with the ultimate goal of identifying novel
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available in the project group of Dr. Julia Madsen-Østerbye, research group of Prof. Philippe Collas, at the Division of Biochemistry, Department of Molecular Medicine, Institute of Basic Medical Sciences
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imaging, metabolomics/lipidomics, extracellular-vesicle-associated molecular profiles, experimental GBM models and patient-level information. The project will also explore how tissue-level metabolic
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cohort of patients with MASLD. Investigate MNP toxicity, accumulation and clearance using patient-derived organoid models. Develop and validate the first tissue-based biological reference materials for MNP
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research program investigating the molecular and developmental mechanisms underlying testicular dysfunction and infertility in a Wnt4 conditional knockout (Wnt4-cKO) mouse model. This position offers
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combination of biochemical and molecular approaches in cultured cells, xenograft models, and genetically engineered mice. The ideal candidate should have valid authorization to work in the United States and a
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molecular biology to establish quantitative structure–function relationships in relevant in vitro models, including 3D tissues. Your tasks As a PhD candidate, you will: Combine colloidal self-assembly and
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targeting these challenging protein regions, using β-catenin as a key model system. FlexCAT brings together academic and non-academic partners and provides an international, interdisciplinary and
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Doc Research Scholar to play a pivotal role in building the lab infrastructure, implementing organoid culture protocols, and performing functional and molecular assays. This position offers a unique
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design rules to understand their chemistry and physics. You will combine coarse-grained and atomistic simulations with surrogate models and experimental insights (with Dr. Baumgartner) to understand