CRISPR-Cas9 nuclear dynamics and target recognition in living cells
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Shaojie Zhang | Maximiliaan Huisman | David Grunwald | Thoru Pederson | Ardalan Naseri | Hanhui Ma | D. Grunwald | Hanhui Ma | Shaojie Zhang | A. Naseri | T. Pederson | Maximiliaan Huisman | Li-Chun Tu | Li-Chun Tu
[1] J. Bähler. Faculty Opinions recommendation of Genome-wide protein-DNA binding dynamics suggest a molecular clutch for transcription factor function. , 2012 .
[2] A. Regev,et al. Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System , 2015, Cell.
[3] Meagan E. Sullender,et al. Optimized sgRNA design to maximize activity and minimize off-target effects of CRISPR-Cas9 , 2015, Nature Biotechnology.
[4] Michael Unser,et al. A pyramid approach to subpixel registration based on intensity , 1998, IEEE Trans. Image Process..
[5] Grigory S. Filonov,et al. Broccoli: Rapid Selection of an RNA Mimic of Green Fluorescent Protein by Fluorescence-Based Selection and Directed Evolution , 2014, Journal of the American Chemical Society.
[6] Le Cong,et al. Multiplex Genome Engineering Using CRISPR/Cas Systems , 2013, Science.
[7] Jennifer A. Doudna,et al. Structures of Cas9 Endonucleases Reveal RNA-Mediated Conformational Activation , 2014, Science.
[8] J. Joung,et al. High-fidelity CRISPR-Cas9 variants with undetectable genome-wide off-targets , 2015, Nature.
[9] L. Banaszynski,et al. A Rapid, Reversible, and Tunable Method to Regulate Protein Function in Living Cells Using Synthetic Small Molecules , 2006, Cell.
[10] David A. Scott,et al. In vivo genome editing using Staphylococcus aureus Cas9 , 2015, Nature.
[11] A. Fire,et al. Distinct patterns of Cas9 mismatch tolerance in vitro and in vivo , 2016, Nucleic acids research.
[12] Konstantin Severinov,et al. Kinetics of the CRISPR-Cas9 effector complex assembly and the role of 3′-terminal segment of guide RNA , 2016, Nucleic acids research.
[13] Luke A. Gilbert,et al. Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression , 2013, Cell.
[14] J. Doudna,et al. A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity , 2012, Science.
[15] M. Rutkauskas,et al. Directional R-Loop Formation by the CRISPR-Cas Surveillance Complex Cascade Provides Efficient Off-Target Site Rejection. , 2015, Cell reports.
[16] Jennifer A. Doudna,et al. A Cas9–guide RNA complex preorganized for target DNA recognition , 2015, Science.
[17] Luke A. Gilbert,et al. CRISPR interference (CRISPRi) for sequence-specific control of gene expression , 2013, Nature Protocols.
[18] Jennifer A. Doudna,et al. DNA interrogation by the CRISPR RNA-guided endonuclease Cas9 , 2014, Nature.
[19] R. Tjian,et al. Dynamics of CRISPR-Cas9 genome interrogation in living cells , 2015, Science.
[20] James E. DiCarlo,et al. RNA-Guided Human Genome Engineering via Cas9 , 2013, Science.
[21] Martin J. Aryee,et al. GUIDE-Seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases , 2014, Nature Biotechnology.
[22] Nicholas E. Propson,et al. Efficient genome engineering in human pluripotent stem cells using Cas9 from Neisseria meningitidis , 2013, Proceedings of the National Academy of Sciences.
[23] Tautvydas Karvelis,et al. Direct observation of R-loop formation by single RNA-guided Cas9 and Cascade effector complexes , 2014, Proceedings of the National Academy of Sciences.
[24] R. Singer,et al. In Vivo Imaging of Labelled Endogenous β-actin mRNA During Nucleocytoplasmic Transport , 2010, Nature.
[25] Shaojie Zhang,et al. Multiplexed labeling of genomic loci with dCas9 and engineered sgRNAs using CRISPRainbow , 2016, Nature Biotechnology.
[26] David A. Scott,et al. Genome-wide binding of the CRISPR endonuclease Cas9 in mammalian cells , 2014, Nature Biotechnology.
[27] P. Stadler,et al. An updated human snoRNAome , 2016, Nucleic acids research.
[28] Jacob E Corn,et al. Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA , 2016, Nature Biotechnology.
[29] Jennifer A. Doudna,et al. Structures of a CRISPR-Cas9 R-loop complex primed for DNA cleavage , 2016, Science.
[30] J. Keith Joung,et al. 731. High-Fidelity CRISPR-Cas9 Nucleases with No Detectable Genome-Wide Off-Target Effects , 2016 .
[31] Wei Zhang,et al. Dynamic Imaging of Genomic Loci in Living Human Cells by an Optimized CRISPR/Cas System , 2014, Cell.
[32] Howard M. Salis,et al. A Biophysical Model of CRISPR/Cas9 Activity for Rational Design of Genome Editing and Gene Regulation , 2016, PLoS Comput. Biol..
[33] Jennifer A. Doudna,et al. Conformational control of DNA target cleavage by CRISPR–Cas9 , 2015, Nature.
[34] Shaojie Zhang,et al. Multicolor CRISPR labeling of chromosomal loci in human cells , 2015, Proceedings of the National Academy of Sciences.
[35] David A. Scott,et al. Rationally engineered Cas9 nucleases with improved specificity , 2015, Science.
[36] James G McNally,et al. Quantitative FRAP in analysis of molecular binding dynamics in vivo. , 2008, Methods in cell biology.
[37] Mazhar Adli,et al. Genome-wide analysis reveals characteristics of off-target sites bound by the Cas9 endonuclease , 2014, Nature Biotechnology.
[38] G. Church,et al. Cas9 gRNA engineering for genome editing, activation and repression , 2015, Nature Methods.
[39] Eli J. Fine,et al. DNA targeting specificity of RNA-guided Cas9 nucleases , 2013, Nature Biotechnology.