BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

444 related articles for article (PubMed ID: 28334779)

  • 21. A multifunctional AAV-CRISPR-Cas9 and its host response.
    Chew WL; Tabebordbar M; Cheng JK; Mali P; Wu EY; Ng AH; Zhu K; Wagers AJ; Church GM
    Nat Methods; 2016 Oct; 13(10):868-74. PubMed ID: 27595405
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Post-translational Regulation of Cas9 during G1 Enhances Homology-Directed Repair.
    Gutschner T; Haemmerle M; Genovese G; Draetta GF; Chin L
    Cell Rep; 2016 Feb; 14(6):1555-1566. PubMed ID: 26854237
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The nontoxic cell cycle modulator indirubin augments transduction of adeno-associated viral vectors and zinc-finger nuclease-mediated gene targeting.
    Rahman SH; Bobis-Wozowicz S; Chatterjee D; Gellhaus K; Pars K; Heilbronn R; Jacobs R; Cathomen T
    Hum Gene Ther; 2013 Jan; 24(1):67-77. PubMed ID: 23072634
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Co-incident insertion enables high efficiency genome engineering in mouse embryonic stem cells.
    Shy BR; MacDougall MS; Clarke R; Merrill BJ
    Nucleic Acids Res; 2016 Sep; 44(16):7997-8010. PubMed ID: 27484482
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A precise gene delivery approach for human induced pluripotent stem cells using Cas9 RNP complex and recombinant AAV6 donor vectors.
    Chupradit K; Thongsin N; Tayapiwatana C; Wattanapanitch M
    PLoS One; 2022; 17(7):e0270963. PubMed ID: 35797389
    [TBL] [Abstract][Full Text] [Related]  

  • 26. One-step high-efficiency CRISPR/Cas9-mediated genome editing in Streptomyces.
    Huang H; Zheng G; Jiang W; Hu H; Lu Y
    Acta Biochim Biophys Sin (Shanghai); 2015 Apr; 47(4):231-43. PubMed ID: 25739462
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Homologous Recombination-Independent Large Gene Cassette Knock-in in CHO Cells Using TALEN and MMEJ-Directed Donor Plasmids.
    Sakuma T; Takenaga M; Kawabe Y; Nakamura T; Kamihira M; Yamamoto T
    Int J Mol Sci; 2015 Oct; 16(10):23849-66. PubMed ID: 26473830
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A Versatile and Efficient Plant Protoplast Platform for Genome Editing by Cas9 RNPs.
    Jiang W; Bush J; Sheen J
    Front Genome Ed; 2021; 3():719190. PubMed ID: 35005700
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Enhanced genome editing to ameliorate a genetic metabolic liver disease through co-delivery of adeno-associated virus receptor.
    Yin S; Ma L; Shao T; Zhang M; Guan Y; Wang L; Hu Y; Chen X; Han H; Shen N; Qiu W; Geng H; Yu Y; Li S; Yu W; Liu M; Li D
    Sci China Life Sci; 2022 Apr; 65(4):718-730. PubMed ID: 32815069
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Insertional Mutagenesis by CRISPR/Cas9 Ribonucleoprotein Gene Editing in Cells Targeted for Point Mutation Repair Directed by Short Single-Stranded DNA Oligonucleotides.
    Rivera-Torres N; Banas K; Bialk P; Bloh KM; Kmiec EB
    PLoS One; 2017; 12(1):e0169350. PubMed ID: 28052104
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Adeno-associated virus inverted terminal repeats stimulate gene editing.
    Hirsch ML
    Gene Ther; 2015 Feb; 22(2):190-5. PubMed ID: 25503695
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Combining Engineered Nucleases with Adeno-associated Viral Vectors for Therapeutic Gene Editing.
    Epstein BE; Schaffer DV
    Adv Exp Med Biol; 2017; 1016():29-42. PubMed ID: 29130152
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The application of CRISPR-Cas9 genome editing in Caenorhabditis elegans.
    Xu S
    J Genet Genomics; 2015 Aug; 42(8):413-21. PubMed ID: 26336798
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Increasing Cas9-mediated homology-directed repair efficiency through covalent tethering of DNA repair template.
    Aird EJ; Lovendahl KN; St Martin A; Harris RS; Gordon WR
    Commun Biol; 2018; 1():54. PubMed ID: 30271937
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of Staphylococcus aureus Cas9: a smaller Cas9 for all-in-one adeno-associated virus delivery and paired nickase applications.
    Friedland AE; Baral R; Singhal P; Loveluck K; Shen S; Sanchez M; Marco E; Gotta GM; Maeder ML; Kennedy EM; Kornepati AV; Sousa A; Collins MA; Jayaram H; Cullen BR; Bumcrot D
    Genome Biol; 2015 Nov; 16():257. PubMed ID: 26596280
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genetic engineering in primary human B cells with CRISPR-Cas9 ribonucleoproteins.
    Wu CM; Roth TL; Baglaenko Y; Ferri DM; Brauer P; Zuniga-Pflucker JC; Rosbe KW; Wither JE; Marson A; Allen CDC
    J Immunol Methods; 2018 Jun; 457():33-40. PubMed ID: 29614266
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Bacterial CRISPR/Cas DNA endonucleases: A revolutionary technology that could dramatically impact viral research and treatment.
    Kennedy EM; Cullen BR
    Virology; 2015 May; 479-480():213-20. PubMed ID: 25759096
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Combining CRISPR/Cas9 and rAAV Templates for Efficient Gene Editing.
    Kaulich M; Dowdy SF
    Nucleic Acid Ther; 2015 Dec; 25(6):287-96. PubMed ID: 26540648
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Self-inactivating, all-in-one AAV vectors for precision Cas9 genome editing via homology-directed repair in vivo.
    Ibraheim R; Tai PWL; Mir A; Javeed N; Wang J; Rodríguez TC; Namkung S; Nelson S; Khokhar ES; Mintzer E; Maitland S; Chen Z; Cao Y; Tsagkaraki E; Wolfe SA; Wang D; Pai AA; Xue W; Gao G; Sontheimer EJ
    Nat Commun; 2021 Nov; 12(1):6267. PubMed ID: 34725353
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Delivering Transgenic DNA Exceeding the Carrying Capacity of AAV Vectors.
    Hirsch ML; Wolf SJ; Samulski RJ
    Methods Mol Biol; 2016; 1382():21-39. PubMed ID: 26611576
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 23.