Héritage Mise à jour dans crispr stop gene silencing through base editing induced nonsense mutations chemise Dégoûter esclave
CRISPR-STOP: Gene silencing through base editing- induced nonsense mutations
PDF] CRISPR base editing applications for identifying cancer-driving mutations | Semantic Scholar
CRISPR-Cas9 Genome Editing for Treatment of Atherogenic Dyslipidemia | Arteriosclerosis, Thrombosis, and Vascular Biology
CRISPR Start-Loss: A Novel and Practical Alternative for Gene Silencing through Base-Editing-Induced Start Codon Mutations: Molecular Therapy - Nucleic Acids
CRISPR-Pass: Gene Rescue of Nonsense Mutations Using Adenine Base Editors - ScienceDirect
CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes through Induction of STOP Codons
Frontiers | Genome Editing for CNS Disorders
Bioorthogonally Activatable Base Editing for On-Demand Pyroptosis | Journal of the American Chemical Society
Clinical and Experimental Pediatrics
Efficient Gene Silencing by Adenine Base Editor-Mediated Start Codon Mutation: Molecular Therapy
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors | Nature Communications
Genes | Free Full-Text | Applications of CRISPR-Cas Technologies to Proteomics
Cells | Free Full-Text | BE4max and AncBE4max Are Efficient in Germline Conversion of C:G to T:A Base Pairs in Zebrafish
65 YEARS OF THE DOUBLE HELIX: The advancements of gene editing and potential application to hereditary cancer in: Endocrine-Related Cancer Volume 25 Issue 8 (2018)
IJMS | Free Full-Text | Dead Cas Systems: Types, Principles, and Applications
CRISPR-STOP: gene silencing through base-editing-induced nonsense mutations | Nature Methods
Applications of genome editing technology in the targeted therapy of human diseases: mechanisms, advances and prospects | Signal Transduction and Targeted Therapy