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Field
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they release their toxic cargo to kill the cancer cells. Methods include, but are not limited to, in vitro culture of primary human cells and cell lines, organ-on-chip models, molecular biology, diverse
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called syncytiotrophoblasts are subsequently damaged, by the altered haemodynamics, however the molecular mechanisms are not fully understood and the impact on haemostasis remains unclear. We aim
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, which has seen little improvement in patient survival over the past decades. Utilizing genetically engineered mouse and human glioma models, our lab investigates how glioma cells interact with the tumor
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adults, characterised by severe genomic instability and a lack of targeted therapies. Using cutting-edge methods and unique primary patient-derived cell models, this project will seek to understand
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methods for single-cell data analysis (tools developed by the team : https://github.com/cantinilab ). Single-cell high-throughput sequencing, extracting huge amounts molecular data from a cell, is creating
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. in microbiology, immunology, systems biology, molecular biology, computational biology, or a related field. • Experience in one or more of the following areas: microbiome research, animal models
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soon as possible at Department of Cardiology, Angiology and Pneumology. The research group "Molecular and Translational Cardiology", headed by Prof. Dr. Patrick Most and Dr. Julia Ritterhoff, focuses
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molecular biology, quantitative imaging and biophysical approaches to investigate cell shape changes in cultured cells and in vivo. Current projects in the lab include investigating the regulation
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• Establishing an in vitro model for therapeutic screening • High throughput screening of several promising molecular therapeutics • Conducting an in vivo study to evaluate the molecular
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an efficient AI foundational exploration of the molecular space. How can we bias the generative models towards desirable molecular properties How can we integrate generative AI models and different molecular