[1] |
Cong, L., Ran, F.A., Cox, D. et al. Multiplex genome engineering using CRISPR/Cas systems Science, 339 (2013),pp. 819-823
|
[2] |
Gao, L., Cox, D.B.T., Yan, W.X. et al. Engineered Cpf1 variants with altered PAM specificities Nat. Biotechnol., 35 (2017),pp. 789-792
|
[3] |
Gaudelli, N.M., Komor, A.C., Rees, H.A. et al. Programmable base editing of A·T to G·C in genomic DNA without DNA cleavage Nature, 551 (2017),pp. 464-471
|
[4] |
He, Y., Zhang, T., Yang, N. et al. Self-cleaving ribozymes enable the production of guide RNAs from unlimited choices of promoters for CRISPR/Cas9 mediated genome editing J. Genet. Genomics, 44 (2017),pp. 469-472
|
[5] |
Hu, J.H., Miller, S.M., Geurts, M.H. et al. Evolved Cas9 variants with broad PAM compatibility and high DNA specificity Nature, 556 (2018),pp. 57-80
|
[6] |
Hu, X., Wang, C., Fu, Y. et al. Expanding the range of CRISPR/Cas9 genome editing in rice Mol. Plant, 9 (2016),pp. 943-945
|
[7] |
Komor, A.C., Kim, Y.B., Packer, M.S. et al. Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage Nature, 533 (2016),pp. 420-424
|
[8] |
Kim, H., Kim, S.-T., Ryu, J. et al. CRISPR/Cpf1-mediated DNA-free plant genome editing Nat. Commun., 8 (2017),p. 14406
|
[9] |
Li, J., Sun, Y., Du, J. et al. Generation of targeted point mutations in rice by a modified CRISPR/Cas9 system Mol. Plant, 10 (2017),pp. 526-529
|
[10] |
Li, S., Zhang, X., Wang, W. et al. Expanding the scope of CRISPR/Cpf1-mediated genome editing in rice Mol. Plant, 11 (2018),pp. 995-998
|
[11] |
Lu, Y., Zhu, J.K. Precise editing of a target base in the rice genome using a modified CRISPR/Cas9 system Mol. Plant, 10 (2017),pp. 523-525
|
[12] |
Ma, X., Zhang, Q., Zhu, Q. et al. A robust CRISPR/Cas9 system for convenient, high-efficiency multiplex genome editing in monocot and dicot plants Mol. Plant, 8 (2015),pp. 1274-1284
|
[13] |
Miao, J., Guo, D., Zhang, J. et al. Targeted mutagenesis in rice using CRISPR-Cas system Cell Res., 23 (2013),pp. 1233-1236
|
[14] |
Nishimasu, H., Shi, X., Ishiguro, S. et al. Engineered CRISPR-Cas9 nuclease with expanded targeting space Science, 361 (2018),p. 1259
|
[15] |
Ran, F.A., Cong, L., Yan, W.X. et al. Nature, 520 (2015),p. 186
|
[16] |
Ren, B., Yan, F., Kuang, Y. et al. Improved base editor for efficiently inducing genetic variations in rice with CRISPR/Cas9-guided hyperactive hAID mutant Mol. Plant, 11 (2018),pp. 623-626
|
[17] |
Tang, X., Lowder, L.G., Zhang, T. et al. A CRISPR-Cpf1 system for efficient genome editing and transcriptional repression in plants Nat. Plants, 3 (2017),p. 17018
|
[18] |
Wang, J., Meng, X., Hu, X. et al. xCas9 expands the scope of genome editing with reduced efficiency in rice Plant Biotechnol. J., 17 (2018),pp. 709-711
|
[19] |
Wang, M., Mao, Y., Lu, Y. et al. Multiplex gene editing in rice using the CRISPR-Cpf1 system Mol. Plant, 10 (2017),pp. 1011-1013
|
[20] |
Zetsche, B., Gootenberg, Jonathan S., Abudayyeh, Omar O. et al. Cpf1 is a single RNA-guided endonuclease of a class 2 CRISPR-Cas system Cell, 163 (2015),pp. 759-771
|