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short and long-read sequencing and transcriptomics, and iPSC-based disease modeling to better understand the genetic etiologies of intractable epilepsy. The team is part of the European STXBP1 consortium
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, this project could be a perfect fit for you. External and internal post-doc researchers who are eligible to submit an FWO or MSCA post-doc application are invited to apply. The top ranked candidate(s) with
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-causing mutations. Finally, we will validate the identified key (epi)genetic molecular and eplore their therapeutic potential in in vitro and in vivo disease models. Profile The candidate should: have an
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reconstruction framework for reproducible estimation of the cerebral blood flow in the mouse brain. Once established, the framework will be applied in animal models of Huntington’s Disease. You will publish
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, will serve as input to generate a statistical prediction model, that will be built together with the bioinformatics team. You will publish scientific articles related to the research project, disseminate
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biological and CRISPR/CAS9 technologies and organoid models derived from CRC patients. You will publish scientific articles related to the research project and will participate to scientific conferences
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, this project could be a perfect fit for you. External and internal post-doc researchers who are eligible to submit an FWO or MSCA post-doc application are invited to apply. The top ranked candidate(s) with