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AD, yet the mechanisms through which it shapes immune responses in the human brain remain poorly understood. This PhD project aims to uncover how genetic risk influences immune cell function in AD by
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Human Stem Cell-based Neural Models is available at the Language & Genetics Department of the Max Planck Institute, Nijmegen, the Netherlands. The position is in the research group of Simon Fisher, co
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to investigate the genetic influences underlying human growth and behaviour in infancy. A central component of the project is the meta-analysis of infant twin studies, with an explicit focus on modelling
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disorder with a prevalence of 1:2,100. The genetic cause of DM1 results from an amplified CTG trinucleotide repeat in the 3’ untranslated region of the DMPK gene. It is well accepted that the expanded CTG
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the Job related to staff position within a Research Infrastructure? No Offer Description Welcome to Maastricht University! What if you could uncover how genetic variation in one of the largest human
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the future of sustainable protein crops in the Netherlands? Are you excited about combining plant physiology, genetics, and cutting-edge phenotyping to advance the protein transition? Then one of these two PhD
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damage is a major driver of human neurodegeneration and aging. DNA damage obstructs elongating RNA polymerase II directly, leading to the initiation of transcription-coupled DNA repair to remove the DNA
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forward to meet you! Facioscapulohumeral muscular dystrophy (FSHD) is a progressive genetic muscle disorder, causing progressive weakness in the face, shoulders, and upper arms. As individuals with FSHD age
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this ambition, we are building a scalable data platform that integrates molecular, genetic, phenotyping, and agronomic datasets. In this role, you play a key part in designing and implementing the technical