SFX by Ex Libris Inc.

Title:	Repair of DNA Double-Strand Breaks by the Nonhomologous End Joining Pathway
Source:	Annual Review of Biochemistry [0066-4154] Stinson, Benjamin yr:2021

Basic

Full text

Full text available via Annual Reviews

Year:

Volume:

Issue:

Start Page:

Document delivery

Request document via Library/Bibliothek

Users interested in this article also expressed an interest in the following:
description	1.	Tsai, Shengdar Q. "GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases." Nature biotechnology 33.2 (2014): 187-197.
description	2.	Kim, D. "Digenome-seq: genome-wide profiling of CRISPR-Cas9 off-target effects in human cells." Nature Methods 12.3 (2015): 237-243.
description	3.	Fu, Y. "High-frequency off-target mutagenesis induced by CRISPR-Cas nucleases in human cells." Nature biotechnology 31.9 (2013): 822-826.
description	4.	Frock, Richard L. "Genome-wide detection of DNA double-stranded breaks induced by engineered nucleases." Nature biotechnology 33.2 (2014): 179-186.
description	5.	Fire, B. X. H. Z. "Landscape of target: guide homology effects on Cas9-mediated cleavage." Nucleic acids research 42.22 (2014): 13778-13787.
description	6.	Kim, J. "Analysis of off-target effects of CRISPR/Cas-derived RNA-guided endonucleases and nickases." Genome research 24.1 (2013): 132-141.
description	7.	Zhang, F. "DNA targeting specificity of RNA-guided Cas9 nucleases." Nature biotechnology 31.9 (2013): 827-832.
description	8.	Zhang, F. "Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity." Cell 154.6 (2013): 1380-1389.
description	9.	Fu, Y. "Improving CRISPR-Cas nuclease specificity using truncated guide RNAs." Nature biotechnology 32.3 (2014): 279-284.
description	10.	Cho, Seung W. "Targeted genome engineering in human cells with the Cas9 RNA-guided endonuclease." Nature biotechnology 31.3 (2013): 230-232.
description	11.	Tsai, Shengdar Q. "CIRCLE-seq: a highly sensitive in vitro screen for genome-wide CRISPR–Cas9 nuclease off-targets." Nature Methods 14.6 (2017): 607-614.
description	12.	Kim, D. "Genome-wide target specificities of CRISPR-Cas9 nucleases revealed by multiplex Digenome-seq." Genome research 26.3 (2016): 406-415.
description	13.	Kleinstiver, Benjamin P. "High-fidelity CRISPR–Cas9 nucleases with no detectable genome-wide off-target effects." Nature 529.7587 (2016): 490-495.
description	14.	Shwartz, V. "Derivation of novel human ground state naive pluripotent stem cells." Nature 504.7479 (2013): 282-286.
description	15.	Burt, A. "Site-specific selfish genes as tools for the control and genetic engineering of natural populations." Proceedings of the Royal Society B: Biological Sciences 270.1518 (2003): 921-928.
description	16.	Robison, Aaron D. "High-throughput single-molecule studies of protein–DNA interactions." FEBS letters 588.19 (2014): 3539-3546.
description	17.	Tsai, Shengdar Q. "Genome Editing: A Tool For Research and Therapy: Towards a functional understanding of variants for molecular diagnostics using genome editing." Nature medicine 20.10 (2014): 1103-1104.
description	18.	Pattanayak, V. "High-throughput profiling of off-target DNA cleavage reveals RNA-programmed Cas9 nuclease specificity." Nature biotechnology 31.9 (2013): 839-843.
description	19.	Charpentier, E. "A Programmable Dual-RNA-Guided DNA Endonuclease in Adaptive Bacterial Immunity." Science 337.6096 (2012): 816-820.
description	20.	Akagi, K., Li, J., Stephens, R. M, Volfovsky, N.,, K. "Extensive variation between inbred mouse strains due to endogenous L1 retrotransposition." Genome research 18.6: 869-880.