No abstract listed.
slender rice, a constitutive gibberellin response mutant, is caused by a null mutation of the SLR1 gene, an ortholog of the height-regulating gene GAI/RGA/RHT/D8
A recombinant polypeptide extends the in vivo half-life of peptides and proteins in a tunable manner
Multiplex and homologous recombination-mediated genome editing in Arabidopsis and Nicotiana benthamiana using guide RNA and Cas9
From classical mutagenesis to nuclease-based breeding - directing natural DNA repair for a natural end-product
CRISPR/Cas9-mediated base-editing system efficiently generates gain-of-function mutations in Arabidopsis
Cas9/sgRNA-based genome editing and other reverse genetic approaches for functional genomic studies in rice
The CRISPR/Cas revolution continues: From efficient gene editing for crop breeding to plant synthetic biology
A method for the production and expedient screening of CRISPR/Cas9-mediated non-transgenic mutant plants
Mimicking natural polymorphism in eIF4E by CRISPR-Cas9 base editing is associated with resistance to potyviruses
Recent developments and applications of genetic transformation and genome editing technologies in wheat.
Improved base excision repair inhibition and bacteriophage Mu Gam protein yields C:G-to-T:A base editors with higher efficiency and product purity
Flax tubulin and CesA superfamilies represent attractive and challenging targets for a variety of genome- and base-editing applications
High-efficient and precise base editing of C•G to T•A in the allotetraploid cotton (Gossypium hirsutum) genome using a modified CRISPR/Cas9 system
Manipulating Cellular Factors to Combat Viruses: A Case Study From the Plant Eukaryotic Translation Initiation Factors eIF4
Application of Cas12a and nCas9-activation-induced cytidine deaminase for genome editing and as a non-sexual strategy to generate homozygous/multiplex edited plants in the allotetraploid genome of tobacco
More precise, more universal and more specific - the next generation of RNA-guided endonucleases for genome editing
Base Editing: The Ever Expanding Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) Tool Kit for Precise Genome Editing in Plants.
Genome Editing for Crop Improvement - Applications in Clonally Propagated Polyploids With a Focus on Potato (Solanum tuberosum L.)
Increasing Cytosine Base Editing Scope and Efficiency With Engineered Cas9-PmCDA1 Fusions and the Modified sgRNA in Rice
Target-specific mutations efficiency at multiple loci of CRISPR/Cas9 system using one sgRNA in soybean.
Discriminated sgRNAs-Based SurroGate System Greatly Enhances the Screening Efficiency of Plant Base-Edited Cells
Prospects of Improving Nitrogen Use Efficiency in Potato: Lessons From Transgenics to Genome Editing Strategies in Plants
A blueprint for gene function analysis through Base Editing in the model plant Physcomitrium (Physcomitrella) patens.
The efficacy of CRISPR-mediated cytosine base editing with the RPS5a promoter in Arabidopsis thaliana.
Expanding plant genome-editing scope by an engineered iSpyMacCas9 system that targets A-rich PAM sequences.
Clustered regularly interspaced short palindromic repeats (CRISPR) are DNA sequences in the genome that are recognized and cleaved by CRISPR-associated proteins (Cas). CRISPR-Cas system enables the editing of genes to create or correct mutations. Discover the latest research on CRISPR here.
CRISPR Ribonucleases Deactivation
CRISPR-Cas system enables the editing of genes to create or correct mutations. This feed focuses on mechanisms that underlie deactivation of CRISPR ribonucleases. Here is the latest research.
CRISPR for Genome Editing
Genome editing technologies enable the editing of genes to create or correct mutations. Clustered regularly interspaced short palindromic repeats (CRISPR) are DNA sequences in the genome that are recognized and cleaved by CRISPR-associated proteins (Cas). Here is the latest research on the use of CRISPR-Cas system in gene editing.