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Postdoc position (d/f/m) developing gene editing therapies for ANO5-related muscular dystrophy Work time full-time Start date 01.04.2026 Employment period limited Application deadline 25.03.2026
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proficient in epigenome-related techniques (DNA methylation and/or histone modifications) and their analysis. Alternatively, the candidate comes with an expertise in CRISPR-based epigenetic editing
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interests, you will have the opportunity to work with: High‑throughput functional genomics: pooled CRISPR and base‑editing screens, barcoded overexpression libraries, massively parallel reporter assays
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biochemistry. Expertise in e.g. CRISPR-mediated gene editing, protein structure prediction, mass spectrometry-based proteomics, or fluorescence microscopy. Expertise and interest in functional analysis
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As part of our team, we are seeking a highly motivated postdoctoral fellow to lead the performance of novel spatial and single-cell profiling in combination with genome-editing approaches in high
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established molecular biology and genetic engineering/genome editing methodologies to enable functional investigation of genes involved in nitrogen fixation. The successful candidate will also perform both
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primary human hematopoietic cells to study myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). The studies include but are not limited to CRISPR gene editing, in vitro differentiation
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with gene editing Experience with organ-on-chip/microphysiological systems or microfluidics, particularly pregnancy on a chip Experience with molecular techniques including siRNA knockdown and gene
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in generating and evaluating human or murine immune cells, gene editing, single cell transcriptomics, flow cytometry, and murine solid tumor models. Eligibility Applicants should be prospective
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Postdoctoral Research Associate - Basic and Translational Research Training in Pediatric Classical H
to the training program. Fellows will receive training in state-of-the-art approaches in bulk and single-cell -omics, gene editing, functional genomics, and in vitro and in vivo models of hematologic