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Starting Grant and an EMBO Installation Grant so your research and training will be well supported for years to come. Check out our lab page for more information: https://www.ceitec.eu/translation-control
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. As part of your PhD training, you will gain hands-on experience with advanced techniques, including CRISPR-Cas9 genome editing, protein and RNA biochemistry and biophysics methods. You’ll also develop
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, genotyping, Western blotting, cell culture. Experience with the following techniques is highly desired: Rodent liver and/or brain survival surgery, ChIP, CRISPR screening, RNAScope, AAV purification, Next-Gen
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age related fibrotic liver diseases. This work will involve genome editing using CRISPR/Cas9 and siRNA techniques both in organoids /cells and in related mouse models - mostly performed by using lipid
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biology ● Mitochondrial and metabolic biology ● Neurobiology and glial biology ● Neuroimmune interactions ● Human genetics and functional genomics ● Single-cell and spatial omics ● CRISPR
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projects independently Ideal Candidates Experience with gene delivery (mRNA, DNA, CRISPR) Background in cartilage, ECM transport, or polyelectrolyte systems Prior exposure to translational or industry-linked
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materials to the safety and function work packages. We are particularly interested in candidates with experience in filamentous fungi, fungal genetics, CRISPR/genome editing, molecular microbiology, reporter
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· CRISPR Knockout and knock in techniques · Ability to plot and interpret data and come up with follow up experiments · Demonstrates mastery of time management · Maintains a high degree of professionalism
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The Jiang Lab, The Icahn School of Medicine at Mount Sinai | New York City, New York | United States | about 2 months ago
The Jiang Lab (https://labs.icahn.mssm.edu/jianglab/) at the Icahn School of Medicine at Mount Sinai, New York is seeking a highly motivated postdoctoral fellow with expertise in genome editing and
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, astrocytes, oligodendrocytes, and microglia. Develop complex neuroimmune co-culture systems incorporating immune cells into human CNS models. Apply CRISPR/Cas-based genome engineering technologies