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interception studies aimed at identifying biological and behavioral targets for preventing progression from premalignant to invasive disease Integration of lifestyle, metabolic, and genomic data to refine early
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state-of-the-art genome engineering, molecular biology, and high-throughput tools to drive discovery and characterisation of new molecular targets both within the sensory nervous system and in other
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: https://rmes.univ-nantes.fr TENS : https://www.inserm-tens.com/home PhAN : https://eng-phan.angers-nantes.hub.inrae.fr TaRGeT: https://umr1089.univ-nantes.fr CEISAM: https://ceisam.univ-nantes.fr/en
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This innovative pipeline aims to identify therapeutic targets to halt MS progression by rejuvenating microglial function. Key Responsibilities Culturing human iPSCs, neural precursor cells, and brain organoids
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targeted and omic approaches to investigate patient-derived materials (fibroblasts and stem cell derived models) and transgenic mice of mitochondrial DNA disorders. We are looking for a creative and highly
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after chemotherapy. Experience and interest in mutation calling from targeted next generation sequencing, whole genome sequencing, and whole exome sequencing approaches is preferred for this position
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Science, Department of Pediatrics, and Gehr Family Center for Leukemia Research. You will directly work on the following projects: 1) Identification of novel therapeutic target using high-throughput CRISPR
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research associate in a post-doctoral position to study CD8 T-cell targeting of human tumor cells via immunopeptidome shift technologies in conjunction with novel T cell receptor (TCR) mechanobiology
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backgrounds, a strong interest in understanding differential protein expression in in vivo samples and development of methods to further assess, identify and validate potential targets is required. Our