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tissues in the joint are affected. Recently, multiple OA risk genes were identified based on small genetic variations (SNPs) in the regulatory sequences of these genes. These variations can lead to
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specifically address whether additional translocations are required to establish new populations on other islands, or to mix genetic variation between already established populations, to protect the species from
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of regenerative medicine, locomotion, genetics and reproduction. More information For more information, please contact Jos Malda external link at j.malda@uu.nl or Riccardo Levato external link at r.levato@uu.nl
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early steps in lung tumor development. You will use cutting-edge techniques including lung organoid models, single-cell transcriptomics and epigenomics, and CRISPR-based genetic perturbation. Key
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language and communication, including departments on genetics, psychology, development, neurobiology and multimodality of these fundamental human abilities. We investigate how children and adults acquire
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to fill evidence gaps; and advancing personalised medicine that incorporates patient preferences and genetic testing. Through these initiatives, ESHPM is at the forefront of shaping healthcare policy and
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child deals with social media, and what influence genetic predisposition and the environment within and outside the family have on this. Valkenburg is one of the leading figures in this field of study