Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuclease Cas9 are enabling the systematic interrogation of mammalian genome function. Analogous to the search function in modern word processors, Cas9 can be guided to specific locations within complex genomes by a short RNA search string. Using this system, DNA sequences within the endogenous genome and their functional outputs are now easily edited or modulated in virtually any organism of choice. Cas9-mediated genetic perturbation is simple and scalable, empowering researchers to elucidate the functional organization of the genome at the systems level and establish causal linkages between genetic variations and biological phenotypes. In this ...
The development of precise and modulated methods for customized manipulation of DNA is an important ...
Gene therapy is based on the principle of the genetic manipulation of DNA or RNA for treating and pr...
Targeted nucleases are powerful genomic tools to precisely change the target genome of living cells,...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
Targeted genome editing technology has been widely used in biomedical studies. The CRISPR-associated...
The Clustered regularly interspaced short palindromic repeat (CRISPR) CRISPR associated 9 (Cas9) sys...
The Clustered regularly interspaced short palindromic repeat (CRISPR) CRISPR associated 9 (Cas9) sys...
Clustered regularly interspaced palindromic repeats (CRISPR)-associated (Cas9) technology has proven...
The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (Cas9) sy...
CRISPR-Cas9 is a RNA-protein complex from adaptive bacterial immune systems that has been repurposed...
CRISPR-Cas9 is a RNA-protein complex from adaptive bacterial immune systems that has been repurposed...
Targeted nucleases are powerful genomic tools to precisely change the target genome of living cells,...
The discovery that the machinery of the Clustered Regularly Interspaced Short Palindromic Repeats (C...
The development of precise and modulated methods for customized manipulation of DNA is an important ...
Gene therapy is based on the principle of the genetic manipulation of DNA or RNA for treating and pr...
Targeted nucleases are powerful genomic tools to precisely change the target genome of living cells,...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
Recent advances in genome engineering technologies based on the CRISPR-associated RNA-guided endonuc...
Targeted genome editing technology has been widely used in biomedical studies. The CRISPR-associated...
The Clustered regularly interspaced short palindromic repeat (CRISPR) CRISPR associated 9 (Cas9) sys...
The Clustered regularly interspaced short palindromic repeat (CRISPR) CRISPR associated 9 (Cas9) sys...
Clustered regularly interspaced palindromic repeats (CRISPR)-associated (Cas9) technology has proven...
The clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated 9 (Cas9) sy...
CRISPR-Cas9 is a RNA-protein complex from adaptive bacterial immune systems that has been repurposed...
CRISPR-Cas9 is a RNA-protein complex from adaptive bacterial immune systems that has been repurposed...
Targeted nucleases are powerful genomic tools to precisely change the target genome of living cells,...
The discovery that the machinery of the Clustered Regularly Interspaced Short Palindromic Repeats (C...
The development of precise and modulated methods for customized manipulation of DNA is an important ...
Gene therapy is based on the principle of the genetic manipulation of DNA or RNA for treating and pr...
Targeted nucleases are powerful genomic tools to precisely change the target genome of living cells,...