3rd International Conference on CRISPR Technologies

Session: Registered Posters

Presentations

Generation and Validation of Human Pluripotent Stem Cell Disease Models Using CRISPR/Cas9 Genome Engineering
Turan, S., Kavyanifar, A., Wend, H., Pozner, T., Loskarn, S., Kaindl, J., Lanfer, J., Rizo, T., Riedlberger, J., Winner, B., Lie, D. C.
Adaptation By T. Thermophilus Type III CRISPR-Cas System in the Presence of Different Phages and Appearance of Viral Escapes
Artamonova, D., Karneyeva, K., Severinov, K., Yasinskaya, A., Milenkin, A.
Evaluation of CRISPR Spacers Diversity in Clostridium Difficile Clinical Isolates
Muzyukina, P., Severinov, K., Savitskaya, E.
Outcomes of Genome Targeting in Bacteria Vary between CRISPR Nucleases
Beisel, C., Yu, Y., Vialetto, E., Collias, D., Barquist, L.
Analysis of Spacers Precursors in Cells Undergoing Naive Adaptation
Savitskaya, E., M. Guzman, N., Musharova, O., Severinov, K., J.M.Mojica, F.
Specificity of Prespacer Choice during CRISPR Adaptation
Vyhovskyi, D., Savitskaya, E., Severinov, K.
CRISPR Array Reconstruction Shields Light on Diversity and Dynamics of Escherichia coli Populations
Savitskaya, E., Rykachevckiy, A., Muzyukina, P., Medvedeva, S., Severinov, K.
Possible Targets for Heterochromatin to Euchromatin Transition of Genes Using CRISPR/dCas9-Mediated Epigenome Editing
Keshavarz Farajkhah, K.
Extensive Self-Targeting By CRISPR-Cas Systems in the Plant Pathogen Xanthomonas Albilineans
Wimmer, F., Beisel, C.
Modular, One-Pot Assembly of CRISPR Arrays Enables Library Generation, Multi-Nuclease Targeting and Reveals Factors Influencing CRISPR RNA Biogenesis
Liao, C., Ttofali, F., Slotkowski, R. A., Denny, S. R., Leenay, R. T., Keung, A., Beisel, C.
A Cas12a-Mediated Crispri Screen for Small Noncoding RNAs in the Human Commensal Bacteroides Thetaiotaomicron
Prezza, G., Ryan, D., Liao, C., Beisel, C., Westermann, A. J.
Binding Does Not Equal Function: Linking Glucocorticoid Receptor Binding to the Regulation of Genes in the Endogenous Genomic Context
Meijsing, S., Thormann, V., Vingron, M., Charpentier, E., Schapflin, R.
Co-Expressing the S. Pyogenes Cas9 and Its Tracrrna Induces Potent, Strain-Specific Cytotoxicity in Lactobacilli
Vento, J., Beisel, C.
Endogenous Tagging Strategies for Accelerated Target Validation and Detection
Ciotta, G., Hock, A., Carter, N., Cuomo, E.
CRISPR/Cas9 meets recombineering in P. putida KT2440
Aparicio, T., de Lorenzo, V., Martanez-Garcaa, E.
Cas9-Based Strategies to Rescue Deep-Intronic Mutations in ABCA4
De Angeli, P., Kohl, S., Reuter, P., Wissinger, B.
CRISPR/Cas9-Mediated Regulation of GAS5-Encoded Box-C/D Small Nucleolar RNAs
Matveeva, A., Julia, F., Evgenii, Z., Grigory, S., Evgenia, B., Sergey, M., Raihan, S. M., Tatiana, G., Dmitry, S., Valentin, V.
Detection of Recbcd-Generated DNA Products in Escherichia coli Cells Undergoing CRISPR Interference
Shiriaeva, A., Savitskaya, E., Kurilovich, E., Metlitskaya, A., Datsenko, K., Semenova, E., Severinov, K.
CRISPR-Cas9 Mediated Knockout of Host Restriction Factors Allows Increasing Influenza A Virus Replication in Human Cell Line
Grigory, S., Sergeeva, M., Vasilieva, A., Eschenko, N., Vasiliev, K., Medvedev, S., Malakhova, A., Evgenii, Z., Richter, V., Komissarov, A.
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
Weber, J.
Natural Diversity of CRISPR Spacers
Medvedeva, S., Severinov, K., Liu, Y., Krupovic, M.
The Impact of Cellular Genome Maintenance Proteins on Primed CRISPR Adaptation By the Escherichia coli Type I-E CRISPR-Cas System
Kurilovich, E., Shiriaeva, A., Metlitskaya, A., Ivan?i?-Ba?e, I., Savitskaya, E., Severinov, K.
DNA Mimic Protein Ocr from Phage T7 Is a Potent Inhibitor of Brex Defence System
Isaev, A., Drobiazko, A., Gordeeva, J., Severinov, K.
Establishing a CRISPR/Cas9 Based System Designed to Explore the Similarities and Differences between Lysyl Oxidases
Nir Zvi, I., Liburkin Dan, T., Kessler, O., Neufeld, G.
Direct Targeting the Expanded CAG Repeat in Huntington's Diseases Using CRISPR/Cas9
Choi, D., Lee, J. M.
Genome Editing for FVIII and AAT Gene Therapy Cures
Lorincz, R., Curiel, D., Dmitriev, I., Lu, Z. H.
Utilizing CRISPR/Cas Technology for Point-of-Care Diagnosis
Franch, O., Bengtson, M., Bharadwaj, M., Torre, J. V. D., Dekker, C.
SuCms1 is a type V CRISPR nuclease variant with a broad PAM preference and tolerance to anti-CRISPR proteins
Dmytrenko, O.
A Novel One-Step Method for Targeted Multiplication of DNA Fragments in Escherichia coli chromosome
Igonina, O., Hook, C., Stoynova, N., Samsonov, V., Krylov, A.
Optimization and Modeling of Crrna Design for Pathogen Detection By Cas13 Enzymes
Schultzhaus, Z., Wang, Z., Stenger, D.
Harnessing Endogenous Repair Mechanisms for Precise Modification of in Vitrofertilized Bovine Embryos
Owen, J., Hennig, S., Paulson, E., Lin, J., Ross, P., Van Eenennaam, A.
In Vivo analysis of CAS1/2-CAS3 Proteins Interaction during Primed Adaptation
Musharova, O., Klimuk, E., Savitskaya, E., Severinov, K.