Results 231-240 of about 1,000
  1. Genome editing tools, particularly the Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) systems (e.g., CRISPR/Cas9), and their repurposing into epigenetic editing platforms, offer enormous potential as safe and customizable
    Date: (2024)
    Authors: Eleanor A. Woodward , Edina Wang , Christopher Wallis , Rohit Sharma ... Pilar Blancafort
    Ref: Epigenome Editing
  2. Date: 2025-01-01
    Authors: Renzl C, Mayer G.
    Journal: Methods in molecular biology (Clifton, N.J.)
  3. Authors: "liweiwei","Xu-Xu Fan","Xue-Jing Cao","Zhao-Yu Zhu","Dan-Shi Pei","Yi-Zhuo Wang","Ji-Yan Zhang",
  4. Authors: "Devansh Agarwal","Kevin W. Mazo","Karl Wahlin",
  5. Unbiased forward genetic screens have been extensively employed in biological research to elucidate functional genomics. In pooled clustered regularly interspaced short palindromic repeats (CRISPR) perturbation screens, various genetically encoded
    Date: (2024)
    Authors: Songhai Tian , Yuhang Qin , Yuxuan Wu , Min Dong
  6. Authors: "Tran Le Cong Huyen Bao Phan","Thomas Macartney","Dario Alessi",
  7. Genetic engineering plays an essential role in the development of cell lines for biopharmaceutical manufacturing. Advanced gene editing tools can improve both the productivity of recombinant cell lines as well as the quality of therapeutic
    Date: (2024)
    Authors: Qiong Wang , Lateef Aliyu , Cheng-Yu Chung , Julian N. Rosenberg ... Michael J. Betenbaugh
    Ref: Recombinant Protein Expression in Mammalian Cells
  8. Authors: "Andrew P. May","Peter Cameron","Alexander H. Settle","Chris K. Fuller","Matthew S. Thompson","A. Mark Cigan","Joshua K. Young",
  9. Clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9 system has been developed as a robust genome engineering tool in a variety of organisms attributed to its high efficiency and versatility. In this chapter, we described the
    Date: (2024)
    Authors: Weizhong Chen , Quanjiang Ji
    Ref: Pseudomonas aeruginosa
  10. The relatively recent discovery of CRISPR/Cas has led to a revolution in our ability to efficiently manipulate the genome of eukaryotic cells. We describe here a protocol that employs CRISPR technology to precisely knock-in a PET imaging reporter
    Date: (2024)
    Authors: Taemoon Chung , Joseph R. Merrill , Scott K. Lyons
    Ref: Positron Emission Tomography
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