BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

291 related articles for article (PubMed ID: 30483052)

  • 1. The Development of an AAV-Based CRISPR SaCas9 Genome Editing System That Can Be Delivered to Neurons
    Kumar N; Stanford W; de Solis C; Aradhana ; Abraham ND; Dao TJ; Thaseen S; Sairavi A; Gonzalez CU; Ploski JE
    Front Mol Neurosci; 2018; 11():413. PubMed ID: 30483052
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Development of a Viral Mediated CRISPR/Cas9 System with Doxycycline Dependent gRNA Expression for Inducible In vitro and In vivo Genome Editing.
    de Solis CA; Ho A; Holehonnur R; Ploski JE
    Front Mol Neurosci; 2016; 9():70. PubMed ID: 27587996
    [TBL] [Abstract][Full Text] [Related]  

  • 3. AAV-CRISPR Gene Editing Is Negated by Pre-existing Immunity to Cas9.
    Li A; Tanner MR; Lee CM; Hurley AE; De Giorgi M; Jarrett KE; Davis TH; Doerfler AM; Bao G; Beeton C; Lagor WR
    Mol Ther; 2020 Jun; 28(6):1432-1441. PubMed ID: 32348718
    [TBL] [Abstract][Full Text] [Related]  

  • 4.
    Li Q; Su J; Liu Y; Jin X; Zhong X; Mo L; Wang Q; Deng H; Yang Y
    Mol Ther Methods Clin Dev; 2021 Mar; 20():652-659. PubMed ID: 33718515
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Split Staphylococcus aureus Cas9 as a Compact Genome-Editing Tool in Plants.
    Kaya H; Ishibashi K; Toki S
    Plant Cell Physiol; 2017 Apr; 58(4):643-649. PubMed ID: 28371831
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Divergent susceptibilities to AAV-SaCas9-gRNA vector-mediated genome-editing in a single-cell-derived cell population.
    Morsy SG; Tonne JM; Zhu Y; Lu B; Budzik K; Krempski JW; Ali SA; El-Feky MA; Ikeda Y
    BMC Res Notes; 2017 Dec; 10(1):720. PubMed ID: 29221488
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A consolidated AAV system for single-cut CRISPR correction of a common Duchenne muscular dystrophy mutation.
    Zhang Y; Nishiyama T; Li H; Huang J; Atmanli A; Sanchez-Ortiz E; Wang Z; Mireault AA; Mammen PPA; Bassel-Duby R; Olson EN
    Mol Ther Methods Clin Dev; 2021 Sep; 22():122-132. PubMed ID: 34485599
    [TBL] [Abstract][Full Text] [Related]  

  • 8. CRISPR/Cas9-mediated genome editing via postnatal administration of AAV vector cures haemophilia B mice.
    Ohmori T; Nagao Y; Mizukami H; Sakata A; Muramatsu SI; Ozawa K; Tominaga SI; Hanazono Y; Nishimura S; Nureki O; Sakata Y
    Sci Rep; 2017 Jun; 7(1):4159. PubMed ID: 28646206
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Editing of the Bacillus subtilis Genome by the CRISPR-Cas9 System.
    Altenbuchner J
    Appl Environ Microbiol; 2016 Sep; 82(17):5421-7. PubMed ID: 27342565
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Promoter Orientation within an AAV-CRISPR Vector Affects Cas9 Expression and Gene Editing Efficiency.
    Fry LE; Peddle CF; Stevanovic M; Barnard AR; McClements ME; MacLaren RE
    CRISPR J; 2020 Aug; 3(4):276-283. PubMed ID: 32833533
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Inhibition of hepatitis B virus replication via HBV DNA cleavage by Cas9 from Staphylococcus aureus.
    Liu Y; Zhao M; Gong M; Xu Y; Xie C; Deng H; Li X; Wu H; Wang Z
    Antiviral Res; 2018 Apr; 152():58-67. PubMed ID: 29458131
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Self-Deleting AAV-CRISPR System for
    Li A; Lee CM; Hurley AE; Jarrett KE; De Giorgi M; Lu W; Balderrama KS; Doerfler AM; Deshmukh H; Ray A; Bao G; Lagor WR
    Mol Ther Methods Clin Dev; 2019 Mar; 12():111-122. PubMed ID: 30619914
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comparison of CRISPR/Cas Endonucleases for
    Li F; Wing K; Wang JH; Luu CD; Bender JA; Chen J; Wang Q; Lu Q; Nguyen Tran MT; Young KM; Wong RCB; Pébay A; Cook AL; Hung SSC; Liu GS; Hewitt AW
    Front Cell Neurosci; 2020; 14():570917. PubMed ID: 33132845
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid, Selection-Free, High-Efficiency Genome Editing in Protozoan Parasites Using CRISPR-Cas9 Ribonucleoproteins.
    Soares Medeiros LC; South L; Peng D; Bustamante JM; Wang W; Bunkofske M; Perumal N; Sanchez-Valdez F; Tarleton RL
    mBio; 2017 Nov; 8(6):. PubMed ID: 29114029
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Lau CH; Suh Y
    F1000Res; 2017; 6():2153. PubMed ID: 29333255
    [TBL] [Abstract][Full Text] [Related]  

  • 16. AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo.
    Hung SS; Chrysostomou V; Li F; Lim JK; Wang JH; Powell JE; Tu L; Daniszewski M; Lo C; Wong RC; Crowston JG; Pébay A; King AE; Bui BV; Liu GS; Hewitt AW
    Invest Ophthalmol Vis Sci; 2016 Jun; 57(7):3470-6. PubMed ID: 27367513
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Factors Impacting Efficacy of AAV-Mediated CRISPR-Based Genome Editing for Treatment of Choroidal Neovascularization.
    Chung SH; Mollhoff IN; Nguyen U; Nguyen A; Stucka N; Tieu E; Manna S; Meleppat RK; Zhang P; Nguyen EL; Fong J; Zawadzki R; Yiu G
    Mol Ther Methods Clin Dev; 2020 Jun; 17():409-417. PubMed ID: 32128346
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Efficient
    Ginn SL; Amaya AK; Liao SHY; Zhu E; Cunningham SC; Lee M; Hallwirth CV; Logan GJ; Tay SS; Cesare AJ; Pickett HA; Grompe M; Dilworth K; Lisowski L; Alexander IE
    JHEP Rep; 2020 Feb; 2(1):100065. PubMed ID: 32039406
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In vivo genome editing using Staphylococcus aureus Cas9.
    Ran FA; Cong L; Yan WX; Scott DA; Gootenberg JS; Kriz AJ; Zetsche B; Shalem O; Wu X; Makarova KS; Koonin EV; Sharp PA; Zhang F
    Nature; 2015 Apr; 520(7546):186-91. PubMed ID: 25830891
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.