December 01, 2015 article Open access Optimizing sgRNA structure to improve CRISPR-Cas9 knockout efficiency Genome biology DOI: 10.1186/s13059-015-0846-3 Full text (OA) OpenAlex Authors 0 Author list not loaded yet. Cited by 8 stored of 369 Search Sort Most cited Newest Oldest Patent citations Title Any typearticle review book-chapter conference-paper preprint dissertation book dataset other Any fieldAgricultural and Biological Sciences Arts and Humanities Biochemistry, Genetics and Molecular Biology Business, Management and Accounting Chemical Engineering Chemistry Computer Science Decision Sciences Dentistry Earth and Planetary Sciences Economics, Econometrics and Finance Energy Engineering Environmental Science Health Professions Immunology and Microbiology Materials Science Mathematics Medicine Neuroscience Nursing Pharmacology, Toxicology and Pharmaceutics Physics and Astronomy Psychology Social Sciences Veterinary Open access Precision genome editing using combinatorial viral vector delivery of CRISPR-Cas9 nucleases and donor DNA constructs 2024 Nucleic Acids Research article Biochemistry, Genetics and Molecular Biology CRISPR and Genetic Engineering Open access cited by 1 patent 15 citations Selection-free precise gene repair using high-capacity adenovector delivery of advanced prime editing systems rescues dystrophin synthesis in DMD muscle cells 2024 Nucleic Acids Research article Biochemistry, Genetics and Molecular Biology CRISPR and Genetic Engineering Open access 24 citations A CRISPR /Cas9‐based multicopy integration system for protein production in Aspergillus niger 2023 FEBS Journal article Biochemistry, Genetics and Molecular Biology Fungal and yeast genetics research Open access 29 citations High-capacity adenovector delivery of forced CRISPR-Cas9 heterodimers fosters precise chromosomal deletions in human cells 2023 Molecular Therapy — Nucleic Acids article Biochemistry, Genetics and Molecular Biology CRISPR and Genetic Engineering Open access 7 citations Large-scale genome editing based on high-capacity adenovectors and CRISPR-Cas9 nucleases rescues full-length dystrophin synthesis in DMD muscle cells 2022 Nucleic Acids Research article Biochemistry, Genetics and Molecular Biology CRISPR and Genetic Engineering Open access 21 citations A primer to gene therapy: Progress, prospects, and problems 2020 Journal of Inherited Metabolic Disease article Biochemistry, Genetics and Molecular Biology Virus-based gene therapy research Open access cited by 4 patents 27 citations High-Capacity Adenoviral Vectors Permit Robust and Versatile Testing of DMD Gene Repair Tools and Strategies in Human Cells 2020 Cells article Biochemistry, Genetics and Molecular Biology Virus-based gene therapy research Open access 30 citations Integrating gene delivery and gene-editing technologies by adenoviral vector transfer of optimized CRISPR-Cas9 components 2020 Gene Therapy article Biochemistry, Genetics and Molecular Biology CRISPR and Genetic Engineering Open access cited by 1 patent 66 citations 8 results References 0