Generation of Centromere-Associated Protein-E CENP-E^-/- Knockout Cell Lines using the CRISPR/Cas9 System

Generation of Transgenic Hydra by Embryo Microinjection

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Efficient iPS Cell Generation from Blood Using Episomes and HDAC Inhibitors

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Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9

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Silencing the Spark: CRISPR/Cas9 Genome Editing in Weakly Electric Fish

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Preparing and Injecting Embryos of Culex Mosquitoes to Generate Null Mutations using CRISPR/Cas9

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Genome Engineering of Primary Human B Cells Using CRISPR/Cas9

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TGF-β-mediated Endothelial to Mesenchymal Transition (EndMT) and the Functional Assessment of EndMT Effectors using CRISPR/Cas9 Gene Editing

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Functional Assessment of Kinesin-7 CENP-E in Spermatocytes Using In Vivo Inhibition, Immunofluorescence and Flow Cytometry

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Construction of Homozygous Mutants of Migratory Locust Using CRISPR/Cas9 Technology

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CRISPR/Cas9 Gene Editing of Hematopoietic Stem and Progenitor Cells for Gene Therapy Applications

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