scholarly article | Q13442814 |
P356 | DOI | 10.1002/CPMB.89 |
P698 | PubMed publication ID | 31237422 |
P2093 | author name string | Jian-Feng Li | |
Zhenxiang Li | |||
Fengzhu Wang | |||
P2860 | cites work | RNA-guided human genome engineering via Cas9 | Q24598394 |
Efficient construction of sequence-specific TAL effectors for modulating mammalian transcription | Q24605428 | ||
Multiplex genome engineering using CRISPR/Cas systems | Q24609428 | ||
Toward controlling gene expression at will: specific regulation of the erbB-2/HER-2 promoter by using polydactyl zinc finger proteins constructed from modular building blocks | Q24645403 | ||
Gene overexpression: uses, mechanisms, and interpretation | Q27001204 | ||
Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana | Q27860555 | ||
Gene Overexpression Resources in Cereals for Functional Genomics and Discovery of Useful Genes | Q28069558 | ||
RNA-guided gene activation by CRISPR-Cas9-based transcription factors | Q28295458 | ||
CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineering | Q29615783 | ||
CRISPR RNA-guided activation of endogenous human genes | Q29617072 | ||
A protein-tagging system for signal amplification in gene expression and fluorescence imaging | Q30604320 | ||
Touchdown PCR for increased specificity and sensitivity in PCR amplification | Q33366975 | ||
RNA-guided transcriptional activation via CRISPR/dCas9 mimics overexpression phenotypes in Arabidopsis | Q33806984 | ||
Agrobacterium-mediated transformation of Arabidopsis thaliana using the floral dip method | Q34003305 | ||
Genome-scale transcriptional activation by an engineered CRISPR-Cas9 complex | Q34042665 | ||
Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. | Q34323082 | ||
Genome-Scale CRISPR-Mediated Control of Gene Repression and Activation | Q34443093 | ||
The presence of multiple introns is essential for ERECTA expression in Arabidopsis | Q35262636 | ||
Highly efficient Cas9-mediated transcriptional programming | Q35372727 | ||
A highly efficient rice green tissue protoplast system for transient gene expression and studying light/chloroplast-related processes | Q35462124 | ||
Comparison of Cas9 activators in multiple species | Q37052928 | ||
Versatile in vivo regulation of tumor phenotypes by dCas9-mediated transcriptional perturbation. | Q37086614 | ||
Multiplexed activation of endogenous genes by CRISPR-on, an RNA-guided transcriptional activator system | Q37214501 | ||
Phenome analysis in plant species using loss-of-function and gain-of-function mutants | Q37259014 | ||
Repurposing CRISPR System for Transcriptional Activation | Q39390088 | ||
The OsSPL16-GW7 regulatory module determines grain shape and simultaneously improves rice yield and grain quality | Q39575698 | ||
Activation tagging: a means of isolating genes implicated as playing a role in plant growth and development | Q40594430 | ||
A Robust CRISPR/Cas9 System for Convenient, High-Efficiency Multiplex Genome Editing in Monocot and Dicot Plants | Q41008314 | ||
Activation tagging in Arabidopsis | Q41729552 | ||
Multiplex and homologous recombination-mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9. | Q42055857 | ||
A modular toolbox for gRNA-Cas9 genome engineering in plants based on the GoldenBraid standard | Q42542096 | ||
A CRISPR/Cas9 Toolbox for Multiplexed Plant Genome Editing and Transcriptional Regulation | Q44859216 | ||
Robust transcriptional activation in plants using multiplexed CRISPR-Act2.0 and mTALE-Act systems. | Q44877573 | ||
RNA-guided transcriptional regulation in planta via synthetic dCas9-based transcription factors. | Q45909715 | ||
Overexpression of receptor-like kinase ERECTA improves thermotolerance in rice and tomato | Q46683474 | ||
A potent Cas9-derived gene activator for plant and mammalian cells | Q47329461 | ||
Activation of a plant gene by T-DNA tagging: auxin-independent growth in vitro | Q48147904 | ||
CRISPR-GE: A Convenient Software Toolkit for CRISPR-Based Genome Editing. | Q52428070 | ||
Direct PCR of intact bacteria (colony PCR). | Q54517256 | ||
DNA sequencing by the dideoxy method. | Q54547151 | ||
The CRISPR tool kit for genome editing and beyond. | Q55233775 | ||
Improved quantitative PCR using nested primers | Q72701548 | ||
Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis | Q80513396 | ||
Enzymatic amplification of DNA by PCR: standard procedures and optimization | Q80673634 | ||
Agarose gel electrophoresis | Q80673757 | ||
Agrobacterium-mediated transformation of rice using immature embryos or calli induced from mature seed | Q81201355 | ||
Quantitative analysis of protein-protein interactions by split firefly luciferase complementation in plant protoplasts | Q88196336 | ||
cis-trans Engineering: Advances and Perspectives on Customized Transcriptional Regulation in Plants | Q88957656 | ||
P433 | issue | 1 | |
P921 | main subject | Cas9 | Q16965677 |
P304 | page(s) | e89 | |
P577 | publication date | 2019-06-01 | |
P1433 | published in | Current protocols in molecular biology | Q26841809 |
P1476 | title | Targeted Transcriptional Activation in Plants Using a Potent Dead Cas9-Derived Synthetic Gene Activator | |
P478 | volume | 127 |