Tapping into the Unsung Potential of CRISPR/CAS Technology in Agriculture

References (232)

1. 1 A Programmable Dual-RNA–Guided DNA Endonuclease in Adaptive Bacterial Immunity [DOI]
2. 2 Multiplex Genome Engineering Using CRISPR/Cas Systems [DOI]
3. 3 RNA-Guided Human Genome Engineering via Cas9 [DOI]
4. 4 Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression [DOI]
5. 5 Cpf1 Is a Single RNA-Guided Endonuclease of a Class 2 CRISPR-Cas System [DOI]
6. 6 CRISPR-Mediated Modular RNA-Guided Regulation of Transcription in Eukaryotes [DOI]
7. 7 Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex [DOI]
8. 8 Genome-Scale CRISPR-Mediated Control of Gene Repression and Activation [DOI]
9. 9 In vivo genome editing using Staphylococcus aureus Cas9 [DOI]
10. 10 A Robust CRISPR/Cas9 System for Convenient, High-Efficiency Multiplex Genome Editing in Monocot and Dicot Plants [DOI]
11. 11 Simultaneous editing of three homoeoalleles in hexaploid bread wheat confers heritable resistance to powdery mildew [DOI]
12. 12 Targeting DNA Double-Strand Breaks with TAL Effector Nucleases [DOI]
13. 13 Targeted genome modification of crop plants using a CRISPR-Cas system [DOI]
14. 14 CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering [DOI]
15. 15 A CRISPR/Cas9 toolkit for multiplex genome editing in plants [DOI]
16. 16 Highly efficient Cas9-mediated transcriptional programming [DOI]
17. 17 A Protein-Tagging System for Signal Amplification in Gene Expression and Fluorescence Imaging [DOI]
18. 18 Boosting CRISPR/Cas9 multiplex editing capability with the endogenous tRNA-processing system [DOI]
19. 19 Multiplex and homologous recombination–mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9 [DOI]
20. 20 Discovery and Functional Characterization of Diverse Class 2 CRISPR-Cas Systems [DOI]
21. 21 DNA-free genome editing in plants with preassembled CRISPR-Cas9 ribonucleoproteins [DOI]
22. 22 Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells [DOI]
23. 23 Increasing the efficiency of precise genome editing with CRISPR-Cas9 by inhibition of nonhomologous end joining [DOI]
24. 24 Targeted mutagenesis in the model plant Nicotiana benthamiana using Cas9 RNA-guided endonuclease [DOI]
25. 25 Efficient genome editing in plants using a CRISPR/Cas system [DOI]
26. 26 Egg cell-specific promoter-controlled CRISPR/Cas9 efficiently generates homozygous mutants for multiple target genes in Arabidopsis in a single generation [DOI]
27. 27 Dimeric CRISPR RNA-guided FokI nucleases for highly specific genome editing [DOI]
28. 28 Engineering Complex Synthetic Transcriptional Programs with CRISPR RNA Scaffolds [DOI]
29. 29 Targeted Chromosomal Cleavage and Mutagenesis in Drosophila Using Zinc-Finger Nucleases [DOI]
30. 30 Multiplexed activation of endogenous genes by CRISPR-on, an RNA-guided transcriptional activator system [DOI]
31. 31 A CRISPR/Cas9 Toolbox for Multiplexed Plant Genome Editing and Transcriptional Regulation [DOI]
32. 32 High-frequency, precise modification of the tomato genome [DOI]
33. 33 Programmable RNA recognition and cleavage by CRISPR/Cas9 [DOI]
34. 34 Broadening the targeting range of Staphylococcus aureus CRISPR-Cas9 by modifying PAM recognition [DOI]
35. 35 DNA Replicons for Plant Genome Engineering [DOI]
36. 36 Turning Meiosis into Mitosis [DOI]
37. 37 Microhomology-based choice of Cas9 nuclease target sites [DOI]
38. 38 The CRISPR / C as system can be used as nuclease for in planta gene targeting and as paired nickases for directed mutagenesis in A rabidopsis resulting in heritable progeny [DOI]
39. 39 Multiplexable, locus-specific targeting of long RNAs with CRISPR-Display [DOI]
40. 40 Transcript-RNA-templated DNA recombination and repair [DOI]
41. 41 Crystal structure of human uracil-DNA glycosylase in complex with a protein inhibitor: Protein mimicry of DNA [DOI]
42. 42 Characterization of Staphylococcus aureus Cas9: a smaller Cas9 for all-in-one adeno-associated virus delivery and paired nickase applications [DOI]
43. 43 Pharmacological inhibition of DNA-PK stimulates Cas9-mediated genome editing [DOI]
44. 44 Gene Therapy for Mitochondrial Disease by Delivering Restriction Endonuclease SmaI into Mitochondria [DOI]
45. 45 CRISPR/Cas mutagenesis of soybean and Medicago truncatula using a new web-tool and a modified Cas9 enzyme [DOI]
46. 46 Manipulating mitochondrial DNA heteroplasmy by a mitochondrially targeted restriction endonuclease [DOI]
47. 47 A chemical compound that stimulates the human homologous recombination protein RAD51 [DOI]
48. 48 YAO is a nucleolar WD40-repeat protein critical for embryogenesis and gametogenesis in Arabidopsis [DOI]
49. 49 The dual nature of homologous recombination in plants [DOI]
50. 50 Correction of mutations within the cystic fibrosis transmembrane conductance regulator by site-directed RNA editing [DOI]
51. 51 Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage [DOI]
52. 52 High-fidelity CRISPR–Cas9 nucleases with no detectable genome-wide off-target effects [DOI]
53. 53 An updated evolutionary classification of CRISPR–Cas systems [DOI]
54. 54 Rationally engineered Cas9 nucleases with improved specificity [DOI]
55. 55 Targeted nucleotide editing using hybrid prokaryotic and vertebrate adaptive immune systems [DOI]
56. 56 Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA [DOI]
57. 57 Efficient and transgene-free genome editing in wheat through transient expression of CRISPR/Cas9 DNA or RNA [DOI]
58. 58 Genome editing in maize directed by CRISPR–Cas9 ribonucleoprotein complexes [DOI]
59. 59 Genome-wide analysis reveals specificities of Cpf1 endonucleases in human cells [DOI]
60. 60 Genome-wide specificities of CRISPR-Cas Cpf1 nucleases in human cells [DOI]
61. 61 New CRISPR–Cas systems from uncultivated microbes [DOI]
62. 62 Efficient targeted multiallelic mutagenesis in tetraploid potato (Solanum tuberosum) by transient CRISPR-Cas9 expression in protoplasts [DOI]
63. 63 Engineering Herbicide-Resistant Rice Plants through CRISPR/Cas9-Mediated Homologous Recombination of Acetolactate Synthase [DOI]
64. 64 Targeted DNA demethylation in vivo using dCas9–peptide repeat and scFv–TET1 catalytic domain fusions [DOI]
65. 65 CRISPR/Cas9 Platforms for Genome Editing in Plants: Developments and Applications [DOI]
66. 66 Multiplexed labeling of genomic loci with dCas9 and engineered sgRNAs using CRISPRainbow [DOI]
67. 67 High-Efficiency Genome Editing in Arabidopsis Using YAO Promoter-Driven CRISPR/Cas9 System [DOI]
68. 68 DNA Repair Profiling Reveals Nonrandom Outcomes at Cas9-Mediated Breaks [DOI]
69. 69 RS-1 enhances CRISPR/Cas9- and TALEN-mediated knock-in efficiency [DOI]
70. 70 Precise Editing of a Target Base in the Rice Genome Using a Modified CRISPR/Cas9 System [DOI]
71. 71 Significant enhancement of fatty acid composition in seeds of the allohexaploid, Camelina sativa , using CRISPR /Cas9 gene editing [DOI]
72. 72 Structure and Engineering of Francisella novicida Cas9 [DOI]
73. 73 Generation of Targeted Point Mutations in Rice by a Modified CRISPR/Cas9 System [DOI]
74. 74 Efficient targeted mutagenesis of rice and tobacco genomes using Cpf1 from Francisella novicida [DOI]
75. 75 Streptococcus thermophilus CRISPR-Cas9 Systems Enable Specific Editing of the Human Genome [DOI]
76. 76 The Neisseria meningitidis CRISPR-Cas9 System Enables Specific Genome Editing in Mammalian Cells [DOI]
77. 77 A scalable strategy for high-throughput GFP tagging of endogenous human proteins [DOI]
78. 78 Site-directed mutagenesis in Petunia × hybrida protoplast system using direct delivery of purified recombinant Cas9 ribonucleoproteins [DOI]
79. 79 Structures of human ADAR2 bound to dsRNA reveal base-flipping mechanism and basis for site selectivity [DOI]
80. 80 Rapid characterization of CRISPR-Cas9 protospacer adjacent motif sequence elements [DOI]
81. 81 High-efficiency CRISPR/Cas9 multiplex gene editing using the glycine tRNA-processing system-based strategy in maize [DOI]
82. 82 Structural Plasticity of PAM Recognition by Engineered Variants of the RNA-Guided Endonuclease Cas9 [DOI]
83. 83 Biallelic Gene Targeting in Rice [DOI]
84. 84 Turning rice meiosis into mitosis [DOI]
85. 85 A Single Transcript CRISPR-Cas9 System for Efficient Genome Editing in Plants [DOI]
86. 86 A modular toolbox for gRNA–Cas9 genome engineering in plants based on the GoldenBraid standard [DOI]
87. 87 Long-term dual-color tracking of genomic loci by modified sgRNAs of the CRISPR/Cas9 system [DOI]
88. 88 Highly specific targeted mutagenesis in plants using Staphylococcus aureus Cas9 [DOI]
89. 89 Expanding the Range of CRISPR/Cas9 Genome Editing in Rice [DOI]
90. 90 Different DNA End Configurations Dictate Which NHEJ Components Are Most Important for Joining Efficiency [DOI]
91. 91 Targeted mutagenesis in rice using CRISPR-Cpf1 system [DOI]
92. 92 Double Nicking by RNA-Guided CRISPR Cas9 for Enhanced Genome Editing Specificity [DOI]
93. 93 731. High-Fidelity CRISPR-Cas9 Nucleases with No Detectable Genome-Wide Off-Target Effects [DOI]
94. 94 CRISPR/Cas9 genome editing of rubber producing dandelion Taraxacum kok-saghyz using Agrobacterium rhizogenes without selection [DOI]
95. 95 Rapid Evolution of Manifold CRISPR Systems for Plant Genome Editing [DOI]
96. 96 Development of a mono-promoter-driven CRISPR/Cas9 system in mammalian cells [DOI]
97. 97 High efficiency of targeted mutagenesis in arabidopsis via meiotic promoter-driven expression of Cas9 endonuclease [DOI]
98. 98 Multiplex CRISPR/Cas9-based genome engineering enhanced by Drosha-mediated sgRNA-shRNA structure [DOI]
99. 99 CRISPR-Cas9-AID base editor is a powerful gain-of-function screening tool [DOI]
100. 100 Optimizing multiplex CRISPR/Cas9-based genome editing for wheat [DOI]
101. 101 Nucleic acid detection with CRISPR-Cas13a/C2c2 [DOI]
102. 102 RNA virus interference via CRISPR/Cas13a system in plants [DOI]
103. 103 Enhanced proofreading governs CRISPR–Cas9 targeting accuracy [DOI]
104. 104 Engineering Quantitative Trait Variation for Crop Improvement by Genome Editing [DOI]
105. 105 Diversity and evolution of class 2 CRISPR–Cas systems [DOI]
106. 106 Efficient DNA-free genome editing of bread wheat using CRISPR/Cas9 ribonucleoprotein complexes [DOI]
107. 107 Precise base editing in rice, wheat and maize with a Cas9-cytidine deaminase fusion [DOI]
108. 108 Targeted base editing in rice and tomato using a CRISPR-Cas9 cytidine deaminase fusion [DOI]
109. 109 Improved base excision repair inhibition and bacteriophage Mu Gam protein yields C:G-to-T:A base editors with higher efficiency and product purity [DOI]
110. 110 DNA-Free Genetically Edited Grapevine and Apple Protoplast Using CRISPR/Cas9 Ribonucleoproteins [DOI]
111. 111 In vivo genome editing with a small Cas9 orthologue derived from Campylobacter jejuni [DOI]
112. 112 Directed evolution of CRISPR-Cas9 to increase its specificity [DOI]
113. 113 CRISPR/Cpf1-mediated DNA-free plant genome editing [DOI]
114. 114 Efficient precise knockin with a double cut HDR donor after CRISPR/Cas9-mediated double-stranded DNA cleavage [DOI]
115. 115 In Vivo Target Gene Activation via CRISPR/Cas9-Mediated Trans-epigenetic Modulation [DOI]
116. 116 Progress and prospects in plant genome editing [DOI]
117. 117 Multiplex Gene Editing in Rice Using the CRISPR-Cpf1 System [DOI]
118. 118 Genome-wide Targeted Mutagenesis in Rice Using the CRISPR/Cas9 System [DOI]
119. 119 Transgenerational CRISPR-Cas9 Activity Facilitates Multiplex Gene Editing in Allopolyploid Wheat [DOI]
120. 120 A potent Cas9-derived gene activator for plant and mammalian cells [DOI]
121. 121 Plant genome editing with TALEN and CRISPR [DOI]
122. 122 Construction of a Genome-Wide Mutant Library in Rice Using CRISPR/Cas9 [DOI]
123. 123 Increased efficiency of targeted mutagenesis by CRISPR/Cas9 in plants using heat stress [DOI]
124. 124 Gene Targeting by Homology-Directed Repair in Rice Using a Geminivirus-Based CRISPR/Cas9 System [DOI]
125. 125 Genome Editing in Cotton with the CRISPR/Cas9 System [DOI]
126. 126 Elimination of Toxic Microsatellite Repeat Expansion RNA by RNA-Targeting Cas9 [DOI]
127. 127 Live cell imaging of low- and non-repetitive chromosome loci using CRISPR-Cas9 [DOI]
128. 128 Robust Transcriptional Activation in Plants Using Multiplexed CRISPR-Act2.0 and mTALE-Act Systems [DOI]
129. 129 Improved Base Editor for Efficiently Inducing Genetic Variations in Rice with CRISPR/Cas9-Guided Hyperactive hAID Mutant [DOI]
130. 130 Multiplex gene regulation by CRISPR-ddCpf1 [DOI]
131. 131 Characterization of the interplay between DNA repair and CRISPR/Cas9-induced DNA lesions at an endogenous locus [DOI]
132. 132 Selectable marker independent transformation of recalcitrant maize inbred B73 and sorghum P898012 mediated by morphogenic regulators BABY BOOM and WUSCHEL2 [DOI]
133. 133 Rapid and reversible epigenome editing by endogenous chromatin regulators [DOI]
134. 134 Generation of a Collection of Mutant Tomato Lines Using Pooled CRISPR Libraries [DOI]
135. 135 Enhanced base editing by co-expression of free uracil DNA glycosylase inhibitor [DOI]
136. 136 Perfectly matched 20-nucleotide guide RNA sequences enable robust genome editing using high-fidelity SpCas9 nucleases [DOI]
137. 137 Harnessing CRISPR/Cas systems for programmable transcriptional and post-transcriptional regulation [DOI]
138. 138 Efficient generation of mice carrying homozygous double-floxp alleles using the Cas9-Avidin/Biotin-donor DNA system [DOI]
139. 139 A CRISPR/Cas9 toolkit for efficient targeted base editing to induce genetic variations in rice [DOI]
140. 140 Editing Citrus Genome via SaCas9/sgRNA System [DOI]
141. 141 Increasing the efficiency of CRISPR‐Cas9‐VQR precise genome editing in rice [DOI]
142. 142 In trans paired nicking triggers seamless genome editing without double-stranded DNA cutting [DOI]
143. 143 Programmable RNA Cleavage and Recognition by a Natural CRISPR-Cas9 System from Neisseria meningitidis [DOI]
144. 144 Gene activation in human cells using CRISPR/Cpf1-p300 and CRISPR/Cpf1-SunTag systems [DOI]
145. 145 Programming sites of meiotic crossovers using Spo11 fusion proteins [DOI]
146. 146 In Planta Processing of the SpCas9–gRNA Complex [DOI]
147. 147 The contribution of homology arms to nuclease-assisted genome engineering [DOI]
148. 148 Generation of stable nulliplex autopolyploid lines of Arabidopsis thaliana using CRISPR/Cas9 genome editing [DOI]
149. 149 DNA Epigenome Editing Using Crispr-Cas Suntag-Directed DNMT3A [DOI]
150. 150 Design and specificity of long ssDNA donors for CRISPR-based knock-in [DOI]
151. 151 Repair of double-strand breaks induced by CRISPR–Cas9 leads to large deletions and complex rearrangements [DOI]
152. 152 Base editing: precision chemistry on the genome and transcriptome of living cells [DOI]
153. 153 Evolved Cas9 variants with broad PAM compatibility and high DNA specificity [DOI]
154. 154 Programmed DNA destruction by miniature CRISPR-Cas14 enzymes [DOI]
155. 155 Engineered CRISPR-Cas9 nuclease with expanded targeting space [DOI]
156. 156 De novo domestication of wild tomato using genome editing [DOI]
157. 157 A high-fidelity Cas9 mutant delivered as a ribonucleoprotein complex enables efficient gene editing in human hematopoietic stem and progenitor cells [DOI]
158. 158 Cytosine, but not adenine, base editors induce genome-wide off-target mutations in rice [DOI]
159. 159 Domestication of wild tomato is accelerated by genome editing [DOI]
160. 160 Functionally diverse type V CRISPR-Cas systems [DOI]
161. 161 Predicting the mutations generated by repair of Cas9-induced double-strand breaks [DOI]
162. 162 Nanoparticle-Mediated Delivery towards Advancing Plant Genetic Engineering [DOI]
163. 163 A highly specific SpCas9 variant is identified by in vivo screening in yeast [DOI]
164. 164 A male-expressed rice embryogenic trigger redirected for asexual propagation through seeds [DOI]
165. 165 CasX enzymes comprise a distinct family of RNA-guided genome editors [DOI]
166. 166 Applications and potential of genome editing in crop improvement [DOI]
167. 167 An APOBEC3A-Cas9 base editor with minimized bystander and off-target activities [DOI]
168. 168 Efficient C-to-T base editing in plants using a fusion of nCas9 and human APOBEC3A [DOI]
169. 169 Site-specific manipulation of Arabidopsis loci using CRISPR-Cas9 SunTag systems [DOI]
170. 170 Genome editing of upstream open reading frames enables translational control in plants [DOI]
171. 171 Engineering of CRISPR-Cas12b for human genome editing [DOI]
172. 172 Clonal seeds from hybrid rice by simultaneous genome engineering of meiosis and fertilization genes [DOI]
173. 173 Optimized base editors enable efficient editing in cells, organoids and mice [DOI]
174. 174 A large-scale whole-genome sequencing analysis reveals highly specific genome editing by both Cas9 and Cpf1 (Cas12a) nucleases in rice [DOI]
175. 175 Precision genome engineering through adenine base editing in plants [DOI]
176. 176 Efficient base editing in methylated regions with a human APOBEC3A-Cas9 fusion [DOI]
177. 177 Repurposing CRISPR-Cas12b for mammalian genome engineering [DOI]
178. 178 CRISPR/Cas9-mediated gene targeting in Arabidopsis using sequential transformation [DOI]
179. 179 Minimal PAM specificity of a highly similar SpCas9 ortholog [DOI]
180. 180 Expanding the base editing scope in rice by using Cas9 variants [DOI]
181. 181 Highly Efficient A·T to G·C Base Editing by Cas9n-Guided tRNA Adenosine Deaminase in Rice [DOI]
182. 182 Programmed Self-Elimination of the CRISPR/Cas9 Construct Greatly Accelerates the Isolation of Edited and Transgene-Free Rice Plants [DOI]
183. 183 Potential high-frequency off-target mutagenesis induced by CRISPR/Cas9 in Arabidopsis and its prevention [DOI]
184. 184 Genome editing in plants by engineered CRISPR–Cas9 recognizing NG PAM [DOI]
185. 185 CRISPR-Sirius: RNA scaffolds for signal amplification in genome imaging [DOI]
186. 186 Plant Genome Editing Using FnCpf1 and LbCpf1 Nucleases at Redefined and Altered PAM Sites [DOI]
187. 187 Genome-wide tracking of dCas9-methyltransferase footprints [DOI]
188. 188 CRISPR/Cas-mediated gene targeting in plants: finally a turn for the better for homologous recombination [DOI]
189. 189 Engineering Introns to Express RNA Guides for Cas9- and Cpf1-Mediated Multiplex Genome Editing [DOI]
190. 190 Precision genome engineering through adenine and cytosine base editing [DOI]
191. 191 Multiplex gene editing in rice with simplified CRISPR‐Cpf1 and CRISPR‐Cas9 systems [DOI]
192. 192 Engineering RNA Virus Interference via the CRISPR/Cas13 Machinery in Arabidopsis [DOI]
193. 193 High-efficiency generation of fertile transplastomic Arabidopsis plants [DOI]
194. 194 Synthesis-dependent repair of Cpf1-induced double strand DNA breaks enables targeted gene replacement in rice [DOI]
195. 195 Multiplexed orthogonal genome editing and transcriptional activation by Cas12a [DOI]
196. 196 Manipulating mRNA splicing by base editing in plants [DOI]
197. 197 A Highly Efficient Cell Division-Specific CRISPR/Cas9 System Generates Homozygous Mutants for Multiple Genes in Arabidopsis [DOI]
198. 198 Advanced editing of the nuclear and plastid genomes in plants [DOI]
199. 199 Three-Component Repurposed Technology for Enhanced Expression: Highly Accumulable Transcriptional Activators via Branched Tag Arrays [DOI]
200. 200 ZFN, TALEN and CRISPR-Cas9 mediated homology directed gene insertion in Arabidopsis: A disconnect between somatic and germinal cells [DOI]
201. 201 Engineered CRISPR-Cas9 nucleases with altered PAM specificities [DOI]
202. 202 CRISPR/Cas Genome Editing and Precision Plant Breeding in Agriculture [DOI]
203. 203 Orthogonal Cas9 proteins for RNA-guided gene regulation and editing [DOI]
204. 204 Crystal Structure of Cpf1 in Complex with Guide RNA and Target DNA [DOI]
205. 205 Transcriptome-wide off-target RNA editing induced by CRISPR-guided DNA base editors [DOI]
206. 206 High aspect ratio nanomaterials enable delivery of functional genetic material without DNA integration in mature plants [DOI]
207. 207 The emerging and uncultivated potential of CRISPR technology in plant science [DOI]
208. 208 One-step genome editing of elite crop germplasm during haploid induction [DOI]
209. 209 CRISPR/Cas-Mediated Base Editing: Technical Considerations and Practical Applications [DOI]
210. 210 CRISPR-Cpf1 mediates efficient homology-directed repair and temperature-controlled genome editing [DOI]
211. 211 Analysis and minimization of cellular RNA editing by DNA adenine base editors [DOI]
212. 212 Increasing Cas9-mediated homology-directed repair efficiency through covalent tethering of DNA repair template [DOI]
213. 213 Application of CRISPR-Cas12a temperature sensitivity for improved genome editing in rice, maize, and Arabidopsis [DOI]
214. 214 Development of a Haploid-Inducer Mediated Genome Editing System for Accelerating Maize Breeding [DOI]
215. 215 An efficient DNA- and selectable-marker-free genome-editing system using zygotes in rice [DOI]
216. 216 Precise insertion and guided editing of higher plant genomes using Cpf1 CRISPR nucleases [DOI]
217. 217 Repurposing CRISPR as an RNA-guided platform for sequence-specific control of gene expression [DOI]
218. 218 Introducing a Spectrum of Long-Range Genomic Deletions in Human Embryonic Stem Cells Using Type I CRISPR-Cas [DOI]
219. 219 Assessment of Cas12a‐mediated gene editing efficiency in plants [DOI]
220. 220 Cas9-NG Greatly Expands the Targeting Scope of the Genome-Editing Toolkit by Recognizing NG and Other Atypical PAMs in Rice [DOI]
221. 221 Genome Engineering in Rice Using Cas9 Variants that Recognize NG PAM Sequences [DOI]
222. 222 CRISPR directed evolution of the spliceosome for resistance to splicing inhibitors [DOI]
223. 223 Precise gene replacement in rice by RNA transcript-templated homologous recombination [DOI]
224. 224 A Cas9 with PAM recognition for adenine dinucleotides [DOI]
225. 225 5′-Modifications improve potency and efficacy of DNA donors for precision genome editing [DOI]
226. 226 Optimizing base editors for improved efficiency and expanded editing scope in rice [DOI]
227. 227 Abscisic Acid Mediated Abiotic Stress Tolerance in Plants [DOI]
228. 228 Plant genome editing using xCas9 with expanded PAM compatibility [DOI]
229. 229 Self-processing of ribozyme-flanked RNAs into guide RNAs in vitro and in vivo for CRISPR-mediated genome editing
230. 230 CRISPR-Cas Mediated Genome Editing: A Paradigm Shift towards Sustainable Agriculture and Biotechnology [DOI]
231. 231 Plant Pan-genomes: A New Frontier in Understanding Genomic Diversity in Plants [DOI]
232. 232 Chromosomal Engineering through CRISPR– Cas Technology: A Way Forward [DOI]

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