Results 541-550 of about 1,000
  1. Date: 2024-01-01
    Authors: Chakraborty M, Powichrowski J, Bruder MR, Nielsen L, Sung C, Boegel SJ, Aucoin MG.
    Journal: Methods in molecular biology (Clifton, N.J.)
  2. The CRISPR/Cas9 system is an extremely powerful tool for targeted mutagenesis in plants. However, plant genome editing relies on the labor-intensive plant regeneration method for generating gene-edited plants. To overcome this bottleneck, several
    Date: (2023)
    Authors: Hyeonjin Kim , Youngbin Oh , Eunae Park , Moonyoung Kang ... Sang-Gyu Kim
    Ref: Base Editors
  3. Date: 2024-01-01
    Authors: Daniel C, Willcocks S, Bhakta S.
    Journal: Methods in molecular biology (Clifton, N.J.)
  4. DNA base editors, one of the CRISPR-based genome editing tools, can induce targeted point mutations at desired sites. Their superiority is based on the fact that they can perform efficient and precise gene editing without generating a DNA
    Date: (2023)
    Authors: Beomjong Song , Sangsu Bae
    Ref: Base Editors
  5. Date: 2024-01-01
    Authors: Inwood S, Cheng K, Betenbaugh MJ, Shiloach J.
    Journal: Methods in molecular biology (Clifton, N.J.)
  6. CRISPR systems can be leveraged to direct recombinases to integrate gene-sized DNA sequences.
    Date: (2023)
    Authors: Lei Tang
  7. Generation of conditional knockout mice using the Cre-loxP system is essential for the analysis of gene functions. The use of CRISPR-Cas9 in combination with two sets of guide RNAs and single-stranded oligonucleotides including loxP sites enables
    Date: (2023)
    Authors: Takuro Horii , Ryosuke Kobayashi , Izuho Hatada
    Ref: Genome Editing in Animals
  8. Transposable element insertions can have broad effects on gene expression, ranging from new regulatory functions to pathogenic consequences by transplanting new cis-regulating elements or perturbing existing ones. Genetic manipulation of such DNA
    Date: (2023)
    Authors: Vivien Marie Weber , Aurélien J. Doucet , Gael Cristofari
    Ref: Transposable Elements
  9. CRISPR base editors are genome-modifying proteins capable of creating single-base substitutions in DNA but without the requirement for a DNA double-strand break. Given their ability to precisely edit DNA, they hold tremendous therapeutic potential.
    Date: (2023)
    Authors: Colin K. Lim , Angelo J. Miskalis , Pablo Perez-Pinera , Thomas Gaj
    Ref: Base Editors
  10. Date: 2024-01-01
    Authors: Poot M.
    Journal: Methods in molecular biology (Clifton, N.J.)
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