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validation assays with guidance as needed. • Assist with gene manipulation workflows, including CRISPR/Cas9 editing and validation, and learn new molecular approaches required for ongoing projects
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culture. · CRISPR /Cas genome editing. · Developmental or cellular disease models. · RNA biology. · Gene-expression or transcriptional regulation. · Noncoding
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development of scalable gene editing platform to engineer therapeutic T cells for clinical trials in inherited disorders. This post will form part of a large, international, collaborative effort focused
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Clelland lab is to develop novel therapies for neurodegenerative diseases including dementias and ALS. Projects are focused on basic mechanisms of disease and CRISPR gene editing in iPSCs, and iPSC
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focused on hematological malignancies, genetics, gene editing, and mouse models. Overview of the position: We are seeking a highly motivated postgraduate research associate interested in joining the
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, Advanced Therapies (CAR-T, gene/cell therapy), Biomedicine, or Bioinformatics applied to health sciences. Proven prior experience in genome editing (CRISPR-Cas9). Proven prior experience in flow
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culture, CRISPR-Cas9-based gene editing, and molecular cloning), data analysis, manuscript preparation, and scientific communication. Please see the Lu lab website for more information about our
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DNA damage, in the Svejstrup lab, DNRF Center of Excellence, Center for Gene Expression (CGEN), Department of Cellular and Molecular Medicine (ICMM), Faculty of Health and Medical Sciences, University
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users. • Utilize and advance tools including gene editing (CRISPR and related), pangenomics, genome assembly, transcriptomics, proteomics, metabolomics, and multi-omics integration. • Collaborate closely
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Specification We are looking for a person with a PhD in molecular biology, cellular biology, biochemistry or a related discipline. You should have practical expertise with gene editing methodologies