BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

444 related articles for article (PubMed ID: 28334779)

  • 1. Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery.
    Gaj T; Staahl BT; Rodrigues GMC; Limsirichai P; Ekman FK; Doudna JA; Schaffer DV
    Nucleic Acids Res; 2017 Jun; 45(11):e98. PubMed ID: 28334779
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Generation of knock-in primary human T cells using Cas9 ribonucleoproteins.
    Schumann K; Lin S; Boyer E; Simeonov DR; Subramaniam M; Gate RE; Haliburton GE; Ye CJ; Bluestone JA; Doudna JA; Marson A
    Proc Natl Acad Sci U S A; 2015 Aug; 112(33):10437-42. PubMed ID: 26216948
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Manufacturing and Delivering Genome-Editing Proteins.
    Liu J; Liang YJ; Ren PL; Gaj T
    Methods Mol Biol; 2018; 1867():253-273. PubMed ID: 30155829
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Enhanced CRISPR/Cas9-mediated precise genome editing by improved design and delivery of gRNA, Cas9 nuclease, and donor DNA.
    Liang X; Potter J; Kumar S; Ravinder N; Chesnut JD
    J Biotechnol; 2017 Jan; 241():136-146. PubMed ID: 27845164
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Virus-Mediated Genome Editing via Homology-Directed Repair in Mitotic and Postmitotic Cells in Mammalian Brain.
    Nishiyama J; Mikuni T; Yasuda R
    Neuron; 2017 Nov; 96(4):755-768.e5. PubMed ID: 29056297
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Versatile and efficient genome editing in human cells by combining zinc-finger nucleases with adeno-associated viral vectors.
    Händel EM; Gellhaus K; Khan K; Bednarski C; Cornu TI; Müller-Lerch F; Kotin RM; Heilbronn R; Cathomen T
    Hum Gene Ther; 2012 Mar; 23(3):321-9. PubMed ID: 21980922
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Engineering Protein-Secreting Plasma Cells by Homology-Directed Repair in Primary Human B Cells.
    Hung KL; Meitlis I; Hale M; Chen CY; Singh S; Jackson SW; Miao CH; Khan IF; Rawlings DJ; James RG
    Mol Ther; 2018 Feb; 26(2):456-467. PubMed ID: 29273498
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CRISPR/Cas9-mediated genome engineering: an adeno-associated viral (AAV) vector toolbox.
    Senís E; Fatouros C; Große S; Wiedtke E; Niopek D; Mueller AK; Börner K; Grimm D
    Biotechnol J; 2014 Nov; 9(11):1402-12. PubMed ID: 25186301
    [TBL] [Abstract][Full Text] [Related]  

  • 9. AAV Vectorization of DSB-mediated Gene Editing Technologies.
    Moser RJ; Hirsch ML
    Curr Gene Ther; 2016; 16(3):207-19. PubMed ID: 27280971
    [TBL] [Abstract][Full Text] [Related]  

  • 10. CRISPR-READI: Efficient Generation of Knockin Mice by CRISPR RNP Electroporation and AAV Donor Infection.
    Chen S; Sun S; Moonen D; Lee C; Lee AY; Schaffer DV; He L
    Cell Rep; 2019 Jun; 27(13):3780-3789.e4. PubMed ID: 31242412
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genome Engineering Using Adeno-associated Virus: Basic and Clinical Research Applications.
    Gaj T; Epstein BE; Schaffer DV
    Mol Ther; 2016 Mar; 24(3):458-64. PubMed ID: 26373345
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Highly efficient homology-driven genome editing in human T cells by combining zinc-finger nuclease mRNA and AAV6 donor delivery.
    Wang J; DeClercq JJ; Hayward SB; Li PW; Shivak DA; Gregory PD; Lee G; Holmes MC
    Nucleic Acids Res; 2016 Feb; 44(3):e30. PubMed ID: 26527725
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Intracellular generation of single-strand template increases the knock-in efficiency by combining CRISPR/Cas9 with AAV.
    Xiao Q; Min T; Ma S; Hu L; Chen H; Lu D
    Mol Genet Genomics; 2018 Aug; 293(4):1051-1060. PubMed ID: 29671068
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Engineered Viruses as Genome Editing Devices.
    Chen X; Gonçalves MA
    Mol Ther; 2016 Mar; 24(3):447-57. PubMed ID: 26336974
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CRISPR/Cas9 Genome Editing in Caenorhabditis elegans: Evaluation of Templates for Homology-Mediated Repair and Knock-Ins by Homology-Independent DNA Repair.
    Katic I; Xu L; Ciosk R
    G3 (Bethesda); 2015 Jun; 5(8):1649-56. PubMed ID: 26044730
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Gene editing using ssODNs with engineered endonucleases.
    Chen F; Pruett-Miller SM; Davis GD
    Methods Mol Biol; 2015; 1239():251-65. PubMed ID: 25408411
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome engineering using Adeno-Associated Virus (AAV).
    Howes R; Schofield C
    Methods Mol Biol; 2015; 1239():75-103. PubMed ID: 25408402
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CRISPR-Mediated Integration of Large Gene Cassettes Using AAV Donor Vectors.
    Bak RO; Porteus MH
    Cell Rep; 2017 Jul; 20(3):750-756. PubMed ID: 28723575
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Homologous Recombination-Based Genome Editing by Clade F AAVs Is Inefficient in the Absence of a Targeted DNA Break.
    Rogers GL; Chen HY; Morales H; Cannon PM
    Mol Ther; 2019 Oct; 27(10):1726-1736. PubMed ID: 31540849
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Designed nucleases for targeted genome editing.
    Lee J; Chung JH; Kim HM; Kim DW; Kim H
    Plant Biotechnol J; 2016 Feb; 14(2):448-62. PubMed ID: 26369767
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.