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Presentations

Cas9-Based Strategies to Rescue Deep-Intronic Mutations in ABCA4
Establishing a CRISPR/Cas9 Based System Designed to Explore the Similarities and Differences between Lysyl Oxidases
In Vivo analysis of CAS1/2-CAS3 Proteins Interaction during Primed Adaptation
Possible Targets for Heterochromatin to Euchromatin Transition of Genes Using CRISPR/dCas9-Mediated Epigenome Editing
Co-Expressing the S. Pyogenes Cas9 and Its Tracrrna Induces Potent, Strain-Specific Cytotoxicity in Lactobacilli
Natural Diversity of CRISPR Spacers
A Novel One-Step Method for Targeted Multiplication of DNA Fragments in Escherichia coli chromosome
Analysis of Spacers Precursors in Cells Undergoing Naive Adaptation
Modular, One-Pot Assembly of CRISPR Arrays Enables Library Generation, Multi-Nuclease Targeting and Reveals Factors Influencing CRISPR RNA Biogenesis
Detection of Recbcd-Generated DNA Products in Escherichia coli Cells Undergoing CRISPR Interference
Genome Editing for FVIII and AAT Gene Therapy Cures
Adaptation By T. Thermophilus Type III CRISPR-Cas System in the Presence of Different Phages and Appearance of Viral Escapes
CRISPR/Cas9 meets recombineering in P. putida KT2440
DNA Mimic Protein Ocr from Phage T7 Is a Potent Inhibitor of Brex Defence System
Harnessing Endogenous Repair Mechanisms for Precise Modification of in Vitrofertilized Bovine Embryos
CRISPR Array Reconstruction Shields Light on Diversity and Dynamics of Escherichia coli Populations
Binding Does Not Equal Function: Linking Glucocorticoid Receptor Binding to the Regulation of Genes in the Endogenous Genomic Context
Precision gene-engineering meets cancer immunotherapy: Targeted insertion of chimeric antigen receptors into the T-cell genome using a novel, virus-free CRISPR/Cas9 knock-in strategy
SuCms1 is a type V CRISPR nuclease variant with a broad PAM preference and tolerance to anti-CRISPR proteins
Outcomes of Genome Targeting in Bacteria Vary between CRISPR Nucleases
CRISPR/Cas9-Mediated Regulation of GAS5-Encoded Box-C/D Small Nucleolar RNAs
Direct Targeting the Expanded CAG Repeat in Huntington's Diseases Using CRISPR/Cas9
Generation and Validation of Human Pluripotent Stem Cell Disease Models Using CRISPR/Cas9 Genome Engineering
Extensive Self-Targeting By CRISPR-Cas Systems in the Plant Pathogen Xanthomonas Albilineans
Endogenous Tagging Strategies for Accelerated Target Validation and Detection
The Impact of Cellular Genome Maintenance Proteins on Primed CRISPR Adaptation By the Escherichia coli Type I-E CRISPR-Cas System
Optimization and Modeling of Crrna Design for Pathogen Detection By Cas13 Enzymes
Specificity of Prespacer Choice during CRISPR Adaptation
A Cas12a-Mediated Crispri Screen for Small Noncoding RNAs in the Human Commensal Bacteroides Thetaiotaomicron
CRISPR-Cas9 Mediated Knockout of Host Restriction Factors Allows Increasing Influenza A Virus Replication in Human Cell Line
Utilizing CRISPR/Cas Technology for Point-of-Care Diagnosis
Evaluation of CRISPR Spacers Diversity in Clostridium Difficile Clinical Isolates

Topics 

Biological Engineering