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→ Apply until 09/07/2024 (DD/MM/YYYY) 23:59 (Brussels time) → Faculty of Medicine and Health Sciences → Department GE31 - Department of Biomolecular Medicine → AAP temporary appointment - 100
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application date Jun 01, 2024 00:00 Department GE31 - Department of Biomolecular Medicine Contract Limited duration Degree Master’s degree in Medicine, Biomedical Sciences, Biotechnology, Bioengineering
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of protein-focused biomolecular and bioinformatics research and engineering technologies. CMB educates and trains the next generation of medical biotechnology researchers and informs the public on the impact
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strategies for successful personal healthcare. We are part of the Department of Biomedical Molecular Biology and the Department of Biomolecular Medicine, with recognised expertise in molecular biology, omics
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the boundaries of protein-focused biomolecular and bioinformatics research and engineering technologies. CMB educates and trains the next generation of medical biotechnology researchers and informs the public
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biomolecular function? We are looking for an experienced postdoctoral researcher with a strong background in modelling of proteins and their interactions, including using empirical force fields, like FoldX. What
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KU Leuven/BioTeC+ (Chemical & Biochemical Process Technology & Control) | Belgium | about 1 month ago
, dynamics, evolution, and manipulation of complex biological systems. Specifically, at CSIC-I2SysBio, the DC will benefit from the expertise in advanced mathematical analysis andcontrol of biomolecular
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into widely applicable research tools, vaccines, diagnostics, and biopharmaceuticals. The research at CMB pushes the boundaries of biomolecular and bioinformatics research and engineering technologies. Your
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this knowledge in the development of novel preventive or therapeutic strategies for successful personal healthcare. We are part of the Department of Biomedical Molecular Biology and the Department of Biomolecular
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/biomolecular-medicine/en/research/research-labs/htad-lab/overview.htm ). Marfan syndrome is a heritable connective tissue disease caused by (likely) pathogenic variants in the gene coding for fibrillin-1 (FBN1