BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

367 related articles for article (PubMed ID: 29056297)

  • 1. 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]  

  • 2. Dynamics and competition of CRISPR-Cas9 ribonucleoproteins and AAV donor-mediated NHEJ, MMEJ and HDR editing.
    Fu YW; Dai XY; Wang WT; Yang ZX; Zhao JJ; Zhang JP; Wen W; Zhang F; Oberg KC; Zhang L; Cheng T; Zhang XB
    Nucleic Acids Res; 2021 Jan; 49(2):969-985. PubMed ID: 33398341
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CRISPR/Cas9 and Agrobacterium tumefaciens virulence proteins synergistically increase efficiency of precise genome editing via homology directed repair in plants.
    Tang Y; Zhang Z; Yang Z; Wu J
    J Exp Bot; 2023 Jun; 74(12):3518-3530. PubMed ID: 36919203
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neuron-Specific Genome Modification in the Adult Rat Brain Using CRISPR-Cas9 Transgenic Rats.
    Bäck S; Necarsulmer J; Whitaker LR; Coke LM; Koivula P; Heathward EJ; Fortuno LV; Zhang Y; Yeh CG; Baldwin HA; Spencer MD; Mejias-Aponte CA; Pickel J; Hoffman AF; Spivak CE; Lupica CR; Underhill SM; Amara SG; Domanskyi A; Anttila JE; Airavaara M; Hope BT; Hamra FK; Richie CT; Harvey BK
    Neuron; 2019 Apr; 102(1):105-119.e8. PubMed ID: 30792150
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homology-directed repair in mouse cells increased by CasRx-mediated knockdown or co-expressing Kaposi's sarcoma-associated herpesvirus ORF52.
    Pan H; Yu W; Zhang M
    Biosci Rep; 2019 Oct; 39(10):. PubMed ID: 31519773
    [TBL] [Abstract][Full Text] [Related]  

  • 6. All-In-One Dendrimer-Based Lipid Nanoparticles Enable Precise HDR-Mediated Gene Editing In Vivo.
    Farbiak L; Cheng Q; Wei T; Álvarez-Benedicto E; Johnson LT; Lee S; Siegwart DJ
    Adv Mater; 2021 Jul; 33(30):e2006619. PubMed ID: 34137093
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CRISPR-Cas9 Genome Editing of Rat Embryos using Adeno-Associated Virus (AAV) and 2-Cell Embryo Electroporation.
    J Davis D; McNew JF; Walls JN; Bethune CE; Oswalt PS; Bryda EC
    J Vis Exp; 2024 Mar; (205):. PubMed ID: 38557598
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome Editing with AAV-BR1-CRISPR in Postnatal Mouse Brain Endothelial Cells.
    Song X; Cui Y; Wang Y; Zhang Y; He Q; Yu Z; Xu C; Ning H; Han Y; Cai Y; Cheng X; Wang J; Teng Y; Yang X; Wang J
    Int J Biol Sci; 2022; 18(2):652-660. PubMed ID: 35002515
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Efficient cancer modeling through CRISPR-Cas9/HDR-based somatic precision gene editing in mice.
    Bu W; Creighton CJ; Heavener KS; Gutierrez C; Dou Y; Ku AT; Zhang Y; Jiang W; Urrutia J; Jiang W; Yue F; Jia L; Ibrahim AA; Zhang B; Huang S; Li Y
    Sci Adv; 2023 May; 9(19):eade0059. PubMed ID: 37172086
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Controlled Cycling and Quiescence Enables Efficient HDR in Engraftment-Enriched Adult Hematopoietic Stem and Progenitor Cells.
    Shin JJ; Schröder MS; Caiado F; Wyman SK; Bray NL; Bordi M; Dewitt MA; Vu JT; Kim WT; Hockemeyer D; Manz MG; Corn JE
    Cell Rep; 2020 Sep; 32(9):108093. PubMed ID: 32877675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Methodologies and Challenges for CRISPR/Cas9 Mediated Genome Editing of the Mammalian Brain.
    Nishizono H; Yasuda R; Laviv T
    Front Genome Ed; 2020; 2():602970. PubMed ID: 34713226
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Adeno-associated virus-mediated gene delivery promotes S-phase entry-independent precise targeted integration in cardiomyocytes.
    Kohama Y; Higo S; Masumura Y; Shiba M; Kondo T; Ishizu T; Higo T; Nakamura S; Kameda S; Tabata T; Inoue H; Motooka D; Okuzaki D; Takashima S; Miyagawa S; Sawa Y; Hikoso S; Sakata Y
    Sci Rep; 2020 Sep; 10(1):15348. PubMed ID: 32948788
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Precise in vivo genome editing via single homology arm donor mediated intron-targeting gene integration for genetic disease correction.
    Suzuki K; Yamamoto M; Hernandez-Benitez R; Li Z; Wei C; Soligalla RD; Aizawa E; Hatanaka F; Kurita M; Reddy P; Ocampo A; Hishida T; Sakurai M; Nemeth AN; Nuñez Delicado E; Campistol JM; Magistretti P; Guillen P; Rodriguez Esteban C; Gong J; Yuan Y; Gu Y; Liu GH; López-Otín C; Wu J; Zhang K; Izpisua Belmonte JC
    Cell Res; 2019 Oct; 29(10):804-819. PubMed ID: 31444470
    [TBL] [Abstract][Full Text] [Related]  

  • 14. CRISPR-Cas9-AAV versus lentivector transduction for genome modification of X-linked severe combined immunodeficiency hematopoietic stem cells.
    Brault J; Liu T; Liu S; Lawson A; Choi U; Kozhushko N; Bzhilyanskaya V; Pavel-Dinu M; Meis RJ; Eckhaus MA; Burkett SS; Bosticardo M; Kleinstiver BP; Notarangelo LD; Lazzarotto CR; Tsai SQ; Wu X; Dahl GA; Porteus MH; Malech HL; De Ravin SS
    Front Immunol; 2022; 13():1067417. PubMed ID: 36685559
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Indel locations are determined by template polarity in highly efficient in vivo CRISPR/Cas9-mediated HDR in Atlantic salmon.
    Straume AH; Kjærner-Semb E; Ove Skaftnesmo K; Güralp H; Kleppe L; Wargelius A; Edvardsen RB
    Sci Rep; 2020 Jan; 10(1):409. PubMed ID: 31941961
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression.
    Gao P; Lyu Q; Ghanam AR; Lazzarotto CR; Newby GA; Zhang W; Choi M; Slivano OJ; Holden K; Walker JA; Kadina AP; Munroe RJ; Abratte CM; Schimenti JC; Liu DR; Tsai SQ; Long X; Miano JM
    Genome Biol; 2021 Mar; 22(1):83. PubMed ID: 33722289
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CRISPR/Cas9 system-mediated impairment of synaptobrevin/VAMP function in postmitotic hippocampal neurons.
    Horvath PM; Kavalali ET; Monteggia LM
    J Neurosci Methods; 2017 Feb; 278():57-64. PubMed ID: 28025172
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prime editing for functional repair in patient-derived disease models.
    Schene IF; Joore IP; Oka R; Mokry M; van Vugt AHM; van Boxtel R; van der Doef HPJ; van der Laan LJW; Verstegen MMA; van Hasselt PM; Nieuwenhuis EES; Fuchs SA
    Nat Commun; 2020 Oct; 11(1):5352. PubMed ID: 33097693
    [TBL] [Abstract][Full Text] [Related]  

  • 19. rAAV capsid mutants eliminate leaky expression from DNA donor template for homologous recombination.
    Ling C; Yu C; Wang C; Yang M; Yang H; Yang K; He Y; Shen Y; Tang S; Yu X; Zhou Z; Zhou S; Zhou J; Zhu L; Li J
    Nucleic Acids Res; 2024 Jun; 52(11):6518-6531. PubMed ID: 38783157
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Streamlining mouse genome editing by integrating AAV repair template delivery and CRISPR-Cas electroporation.
    Moncaut N
    Lab Anim (NY); 2024 May; 53(5):115-116. PubMed ID: 38600182
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.