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experiments involving gene editing technologies in renal systems. Develop and optimize delivery strategies for genetic therapies. Perform advanced molecular, cellular, and tissue analyses (e.g., flow cytometry
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organisms, the project focuses on uncovering the molecular basis of lactose utilization in eukaryotic microorganisms. The work combines bioinformatic and comparative genomic analyses to identify key genes and
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for treatments. Increasing our understanding of the underlying molecular disease mechanisms will aid in the development treatment strategies. We have previously identified that mutations in the genes Col4a1 and
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of cell and gene therapy for selected rare diseases. We cooperate with the Fraunhofer Institute IZI (Germany), the University of Leipzig (Germany) and the University of Copenhagen (Denmark
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, and in vivo imaging • Exposure to mRNA/siRNA delivery or gene-editing systems • Solid publication record and strong communication skills Appointment and Benefits • Full-time position with an initial one
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(e.g. Gibson, Goldengate), CRISPR-mediated gene editing (particularly to edit RNA), lentivirus handling, fluourescent cell imaging, flow cytometry,in vivo mice experiments, next generation sequencing
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(2025), where CRISPR-Cas9 gene editing successfully created artificial protein supercomplexes that enhanced photosynthetic performance in algae. The Challenge : Photosynthesis underpins all life on Earth
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gene expression regulation. Main responsibilities include cell culture of mammalian cells, molecular biology and biochemical experiments. Your profile Applicants should have a degree as “Laborant/in
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Progenitors to Deliver Regenerative Medicine and Disease Modelling”), the project builds on our recent breakthrough findings (The EMBO Journal, 2025) revealing a pivotal role for the transcription factor HAND1
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Cytotoxicity studies Cell signaling analysis Protein function analysis Gene editing and expression analysis - International and Friendly Environment Join a diverse team of researchers in a well-equipped lab with