Cited by 123

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Optimization of Genome Engineering Approaches with the CRISPR/Cas9 System

Li, Kai, Wang, Gang, Andersen, Troels, Zhou, Pingzhu, Pu, William T.·2014·PLoS ONE

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Crossref · 10.1371/journal.pone.0105779

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  • Due to the high efficiency of Cas9 activity and the relatively higher efficiency of NHEJ when compared to HDR, three kinds of entities coexist in this process: wild-type sequences, NHEJ-repaired sequences, and a smaller population of the intended HDR-repaired sequence.

    “Due to the high efficiency of Cas9 activity and the relatively higher efficiency of NHEJ when compared to HDR, three kinds of entities coexist in this process: wild-type sequences, NHEJ-repaired sequences, and a smaller population of the intended HDR-repaired sequence [73].”

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Research works printed but not linked: 14

  1. D Hockemeyer, 2011, Genetic engineering of human pluripotent cells using TALE nucleases, Nat Biotechnol, 29, 731, 10.1038/nbt.1927 · DOI
  2. T Cermak, 2011, Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting, Nucleic Acids Res, 39, e82, 10.1093/nar/gkr218 · DOI
  3. L Cong, 2013, Multiplex genome engineering using CRISPR/Cas systems, Science, 339, 819, 10.1126/science.1231143 · DOI · Paper page
  4. Mali P, Yang L, Esvelt KM, Aach J, Guell M, <etal>et al</etal>.. (2013) RNA-Guided Human Genome Engineering via Cas9. Science. · DOI · Paper page
  5. L Yang, 2013, Optimization of scarless human stem cell genome editing, Nucleic Acids Res, 41, 9049, 10.1093/nar/gkt555 · DOI
  6. Y Miyaoka, 2014, Isolation of single-base genome-edited human iPS cells without antibiotic selection, Nat Methods, 11, 291, 10.1038/nmeth.2840 · DOI
  7. P Liu, 2003, A highly efficient recombineering-based method for generating conditional knockout mutations, Genome Res, 13, 476, 10.1101/gr.749203 · DOI
  8. DG Gibson, 2009, Enzymatic assembly of DNA molecules up to several hundred kilobases, Nat Methods, 6, 343, 10.1038/nmeth.1318 · DOI
  9. P Zhou, 2013, Interrogating translational efficiency and lineage-specific transcriptomes using ribosome affinity purification, Proc Natl Acad Sci U S A, 110, 15395, 10.1073/pnas.1304124110 · DOI
  10. FA Ran, 2013, Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity, Cell, 154, 1380, 10.1016/j.cell.2013.08.021 · DOI · Paper page
  11. Shen B, Zhang W, Zhang J, Zhou J, Wang J, <etal>et al</etal>.. (2014) Efficient genome modification by CRISPR-Cas9 nickase with minimal off-target effects. Nat Methods. · DOI · Paper page
  12. E de Boer, 2003, Efficient biotinylation and single-step purification of tagged transcription factors in mammalian cells and transgenic mice, Proc Natl Acad Sci U S A, 100, 7480, 10.1073/pnas.1332608100 · DOI
  13. I Zhidkov, 2011, CHILD: a new tool for detecting low-abundance insertions and deletions in standard sequence traces, Nucleic Acids Res, 39, e47, 10.1093/nar/gkq1354 · DOI
  14. A Hendel, 2014, Quantifying genome-editing outcomes at endogenous loci with SMRT sequencing, Cell Rep, 7, 293, 10.1016/j.celrep.2014.02.040 · DOI

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Metadata

Authors
Li, K., Wang, G., Andersen, T., Zhou, P., & Pu, W. T.
Venue
PLoS ONE
Published
2014-08-28
Volume
9
Issue
8
Pages
e105779
ISSN
1932-6203
Cited by
123
References
4
Language
en

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