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. The models will help interpret how different damage scenarios affect the ambient vibration signature. Both black-box and white-box damage identification algorithms will be assessed. The resulting digital twin
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MV-CT workflow for historical waste characterization at SCK CEN’s LNK (Laboratory of nuclear calibrations) facility. Key innovations include advanced physics-informed reconstruction algorithms and
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signature. Both black-box and white-box damage identification algorithms will be assessed. The resulting digital twin will serve as the foundation for a permanent SHM system for the galleries in the HADES URL
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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
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from strong hybridization barriers and does not fully exploit available genetic variation. To address this, an international consortium consisting of local breeding institutes in Asia and Africa
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Autosomal dominant polycystic kidney disease (ADPKD) is the leading genetic cause of end-stage kidney disease, affecting over 12 million patients worldwide. Loss-of-function mutations in PKD1 (accounting
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is to integrate genetics, cell biology, genomics, and bio-computing to unravel plant biological processes and to further translate this knowledge into value for society. Please visit us at
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unique advantages for drug and radionuclide delivery due to their biocompatibility, structural regularity and capacity for precise genetic modification. By integrating tumor-targeting ligands, radiometal
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nucleolar organization. We combine molecular genetics, cell biology, biochemistry, and high-resolution sequencing (short- and long-read) to understand how ribosome production is regulated in health and
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the genetic etiology and developing diagnostics and treatment methods for these diseases. Approaches range from human genetics, genomics, protein biochemistry and neuronal and glial cell biology to integrative