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CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes  through Induction of STOP Codons
CRISPR-Mediated Base Editing Enables Efficient Disruption of Eukaryotic Genes through Induction of STOP Codons

CRISPR-STOP: gene silencing through base-editing-induced nonsense mutations  | Nature Methods
CRISPR-STOP: gene silencing through base-editing-induced nonsense mutations | Nature Methods

CRISPR Start-Loss: A Novel and Practical Alternative for Gene Silencing  through Base-Editing-Induced Start Codon Mutations: Molecular Therapy -  Nucleic Acids
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:  Molecular Therapy
CRISPR-Pass: Gene Rescue of Nonsense Mutations Using Adenine Base Editors: Molecular Therapy

CRISPR-Pass: Gene Rescue of Nonsense Mutations Using Adenine Base Editors -  ScienceDirect
CRISPR-Pass: Gene Rescue of Nonsense Mutations Using Adenine Base Editors - ScienceDirect

Functional interrogation of DNA damage response variants with base editing  screens - ScienceDirect
Functional interrogation of DNA damage response variants with base editing screens - ScienceDirect

CRISPR/Cas gene therapy - Zhang - 2021 - Journal of Cellular Physiology -  Wiley Online Library
CRISPR/Cas gene therapy - Zhang - 2021 - Journal of Cellular Physiology - Wiley Online Library

CRISPR/Cas gene therapy - Zhang - 2021 - Journal of Cellular Physiology -  Wiley Online Library
CRISPR/Cas gene therapy - Zhang - 2021 - Journal of Cellular Physiology - Wiley Online Library

Base Editing
Base Editing

i-Silence, Please! An Alternative for Gene Disruption via Adenine Base  Editors: Molecular Therapy
i-Silence, Please! An Alternative for Gene Disruption via Adenine Base Editors: Molecular Therapy

CRISPR/Cas9-mediated genome editing induces gene knockdown by altering the  pre-mRNA splicing in mice | BMC Biotechnology | Full Text
CRISPR/Cas9-mediated genome editing induces gene knockdown by altering the pre-mRNA splicing in mice | BMC Biotechnology | Full Text

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)
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)

Frontiers | Delivery Platforms for CRISPR/Cas9 Genome Editing of Glial  Cells in the Central Nervous System
Frontiers | Delivery Platforms for CRISPR/Cas9 Genome Editing of Glial Cells in the Central Nervous System

Cells | Free Full-Text | BE4max and AncBE4max Are Efficient in Germline  Conversion of C:G to T:A Base Pairs in Zebrafish
Cells | Free Full-Text | BE4max and AncBE4max Are Efficient in Germline Conversion of C:G to T:A Base Pairs in Zebrafish

In situ CRISPR‐Cas9 base editing for the development of genetically  engineered mouse models of breast cancer | The EMBO Journal
In situ CRISPR‐Cas9 base editing for the development of genetically engineered mouse models of breast cancer | The EMBO Journal

Clinical and Experimental Pediatrics
Clinical and Experimental Pediatrics

Current Status and Challenges of DNA Base Editing Tools - ScienceDirect
Current Status and Challenges of DNA Base Editing Tools - ScienceDirect

Genes | Free Full-Text | Applications of CRISPR-Cas Technologies to  Proteomics
Genes | Free Full-Text | Applications of CRISPR-Cas Technologies to Proteomics

CRISPR base editing and prime editing: DSB and template-free editing  systems for bacteria and plants - ScienceDirect
CRISPR base editing and prime editing: DSB and template-free editing systems for bacteria and plants - ScienceDirect

CRISPR-Cas9 Genome Editing for Treatment of Atherogenic Dyslipidemia |  Arteriosclerosis, Thrombosis, and Vascular Biology
CRISPR-Cas9 Genome Editing for Treatment of Atherogenic Dyslipidemia | Arteriosclerosis, Thrombosis, and Vascular Biology

PDF) CRISPR-STOP: gene silencing through base-editing-induced nonsense  mutations
PDF) CRISPR-STOP: gene silencing through base-editing-induced nonsense mutations

Highly efficient multiplex human T cell engineering without double-strand  breaks using Cas9 base editors | Nature Communications
Highly efficient multiplex human T cell engineering without double-strand breaks using Cas9 base editors | Nature Communications

IJMS | Free Full-Text | Dead Cas Systems: Types, Principles, and  Applications
IJMS | Free Full-Text | Dead Cas Systems: Types, Principles, and Applications

CRISPR-Cas9 base editors and their current role in human therapeutics -  Cytotherapy
CRISPR-Cas9 base editors and their current role in human therapeutics - Cytotherapy

Bioorthogonally Activatable Base Editing for On-Demand Pyroptosis | Journal  of the American Chemical Society
Bioorthogonally Activatable Base Editing for On-Demand Pyroptosis | Journal of the American Chemical Society

CRISPR-STOP: Gene silencing through base editing- induced nonsense mutations
CRISPR-STOP: Gene silencing through base editing- induced nonsense mutations

Bioorthogonally Activatable Base Editing for On-Demand Pyroptosis | Journal  of the American Chemical Society
Bioorthogonally Activatable Base Editing for On-Demand Pyroptosis | Journal of the American Chemical Society