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related to these general topics. Each focuses on gene regulation â“ and changes that occur in gene regulation â“ during stem cell development and differentiation. We use mice to model pediatric malignancies
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models using induced pluripotent stem cell (iPSC)-derived kidney organoids. A key aspect of this work will involve integrating bioprinting and organ-on-chip technologies to create mature and
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Department: Tomáš Bárta Research Group: Stem Cell Biology and Vision Research – Faculty of Medicine Deadline: 31 Jan 2026 Start date: April 2026 or upon agreement Job type: full-time Job field
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topics. Each focuses on gene regulation – and changes that occur in gene regulation – during stem cell development and differentiation. We use mice to model pediatric malignancies. The overall goal of our
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vivo culture models, primary cell models and stem cell models. Beyond experimental work, you will also play a key role in an in vitro model validation project. Your contributions will involve daily
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metabolism and drug transport. Examples of this include cell-based models such as induced-pluripotent stem cells, primary human hepatocytes, and clinical studies. The pharmacoepidemiological research group
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organoid-based research. For more information go to: https://www.bauschlab.org Your Qualification: High motivation, curiosity, and commitment to scientific excellence PhD in stem cell biology, developmental
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the liver microenvironment. Experiments will utilize animal models, cell culture including induced pluripotent stem cells, and human patient samples. Required Qualifications: Applicants should hold a PhD
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system (CNS). We aim to uncover the principles of gene expression regulation during development and repurpose them for regeneration. We use a multidisciplinary approach that involves stem cell biology
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-1209; Nature, 2019, Mar; 567(7746):113-117; Cell Stem Cell, 2018, Oct 4; 23(4):557; NatureCommunications, 2017 Nov 15;8(1):1523; TheEMBO Journal, 2016 Jan 4;35(1):24-45; J Cell Science, 2015 Dec 1;128(23