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, and society. We're proud of our strong reputation in molecular biology and biotechnology, but even more of the people behind it. Currently, we are looking for a Learning & Development manager Do you
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medical development are welcome and we might actually recruit two persons with complementary expertise. Additional information may be found in the following selected references: De Strooper, B. & Karran, E
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developing genetic risk scores as biomarkers for neurological disorders. The Rademakers lab leads cutting-edge research into risk genes and molecular mechanisms in Frontotemporal Dementia (FTD), while
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diverse classes of inhibitory neurons are specified and integrated into brain circuits during development. Our work bridges developmental neurobiology, disease modeling, and systems neuroscience. To do
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Postdoctoral position to study species-specific mechanisms of gene regulation in human neurons. The Vanderhaeghen Lab (https://pvdhlab.org ) and the Aerts Lab (www.aertslab.org ) at VIB KULeuven are seeking creative postdoctoral scientists to study the human-specific mechanisms of gene...
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human-specific features of brain development influence early cortical circuit function and the pathophysiology of autism spectrum disorders (ASD) Research Project “Linking human-specific synaptic
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supported by a Foundation against Cancer (2025 – 2030). We have developed in vivo single-cell CRISPR technologies to screen for dozens of molecular factors in tumor-associated macrophages (TAMs) in vivo. We
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Alzheimer’s disease to develop and/or apply computational approaches to large scale genomic or transcriptomic datasets for identification of targets for early detection, prevention or treatment of Alzheimer’s
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preparation. Perform daily maintenance and quality control of flow cytometers and cell sorters. Assist researchers with sample preparation, acquisition, and data analysis (e.g., FlowJo). Train users
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the development of genetic autoinflammatory diseases. Using techniques in cell biology, molecular biology and biophysics you will investigate how loss of function of the RNA editing enzyme ADAR1 causes the human