These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 32646486)

  • 21. Genome editing through large insertion leads to the skipping of targeted exon.
    Uddin B; Chen NP; Panic M; Schiebel E
    BMC Genomics; 2015 Dec; 16():1082. PubMed ID: 26691863
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Postnatal Cardiac Gene Editing Using CRISPR/Cas9 With AAV9-Mediated Delivery of Short Guide RNAs Results in Mosaic Gene Disruption.
    Johansen AK; Molenaar B; Versteeg D; Leitoguinho AR; Demkes C; Spanjaard B; de Ruiter H; Akbari Moqadam F; Kooijman L; Zentilin L; Giacca M; van Rooij E
    Circ Res; 2017 Oct; 121(10):1168-1181. PubMed ID: 28851809
    [TBL] [Abstract][Full Text] [Related]  

  • 23. One-step generation of complete gene knockout mice and monkeys by CRISPR/Cas9-mediated gene editing with multiple sgRNAs.
    Zuo E; Cai YJ; Li K; Wei Y; Wang BA; Sun Y; Liu Z; Liu J; Hu X; Wei W; Huo X; Shi L; Tang C; Liang D; Wang Y; Nie YH; Zhang CC; Yao X; Wang X; Zhou C; Ying W; Wang Q; Chen RC; Shen Q; Xu GL; Li J; Sun Q; Xiong ZQ; Yang H
    Cell Res; 2017 Jul; 27(7):933-945. PubMed ID: 28585534
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A novel human muscle cell model of Duchenne muscular dystrophy created by CRISPR/Cas9 and evaluation of antisense-mediated exon skipping.
    Shimo T; Hosoki K; Nakatsuji Y; Yokota T; Obika S
    J Hum Genet; 2018 Mar; 63(3):365-375. PubMed ID: 29339778
    [TBL] [Abstract][Full Text] [Related]  

  • 25. One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering.
    Wang H; Yang H; Shivalila CS; Dawlaty MM; Cheng AW; Zhang F; Jaenisch R
    Cell; 2013 May; 153(4):910-8. PubMed ID: 23643243
    [TBL] [Abstract][Full Text] [Related]  

  • 26. CRISPR/Cas9-mediated genome editing of splicing mutation causing congenital hearing loss.
    Ryu N; Kim MA; Choi DG; Kim YR; Sonn JK; Lee KY; Kim UK
    Gene; 2019 Jun; 703():83-90. PubMed ID: 30898719
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Splice donor site sgRNAs enhance CRISPR/Cas9-mediated knockout efficiency.
    García-Tuñón I; Alonso-Pérez V; Vuelta E; Pérez-Ramos S; Herrero M; Méndez L; Hernández-Sánchez JM; Martín-Izquierdo M; Saldaña R; Sevilla J; Sánchez-Guijo F; Hernández-Rivas JM; Sánchez-Martín M
    PLoS One; 2019; 14(5):e0216674. PubMed ID: 31071190
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Adenine base-editing-mediated exon skipping induces gene knockout in cultured pig cells.
    Zhu XX; Pan JS; Lin T; Yang YC; Huang QY; Yang SP; Qu ZX; Lin ZS; Wen JC; Yan AF; Feng J; Liu L; Zhang XL; Lu JH; Tang DS
    Biotechnol Lett; 2022 Jan; 44(1):59-76. PubMed ID: 34997407
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Efficient CRISPR/Cas9-assisted gene targeting enables rapid and precise genetic manipulation of mammalian neural stem cells.
    Bressan RB; Dewari PS; Kalantzaki M; Gangoso E; Matjusaitis M; Garcia-Diaz C; Blin C; Grant V; Bulstrode H; Gogolok S; Skarnes WC; Pollard SM
    Development; 2017 Feb; 144(4):635-648. PubMed ID: 28096221
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genome-Wide Off-Target Analysis in CRISPR-Cas9 Modified Mice and Their Offspring.
    Dong Y; Li H; Zhao L; Koopman P; Zhang F; Huang JX
    G3 (Bethesda); 2019 Nov; 9(11):3645-3651. PubMed ID: 31492696
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Unexpected extra exon skipping in the DYSF gene during restoring the reading frame by CRISPR/Cas9.
    Levchenko O; Panchuk I; Kochergin-Nikitsky K; Petrova I; Nagieva S; Pilkin M; Yakovlev I; Smirnikhina S; Deev R; Lavrov A
    Biosystems; 2024 Jan; 235():105072. PubMed ID: 37944631
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Biological plasticity rescues target activity in CRISPR knock outs.
    Smits AH; Ziebell F; Joberty G; Zinn N; Mueller WF; Clauder-Münster S; Eberhard D; Fälth Savitski M; Grandi P; Jakob P; Michon AM; Sun H; Tessmer K; Bürckstümmer T; Bantscheff M; Steinmetz LM; Drewes G; Huber W
    Nat Methods; 2019 Nov; 16(11):1087-1093. PubMed ID: 31659326
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Full-length dystrophin restoration via targeted exon integration by AAV-CRISPR in a humanized mouse model of Duchenne muscular dystrophy.
    Pickar-Oliver A; Gough V; Bohning JD; Liu S; Robinson-Hamm JN; Daniels H; Majoros WH; Devlin G; Asokan A; Gersbach CA
    Mol Ther; 2021 Nov; 29(11):3243-3257. PubMed ID: 34509668
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Simple generation of albino C57BL/6J mice with G291T mutation in the tyrosinase gene by the CRISPR/Cas9 system.
    Mizuno S; Dinh TT; Kato K; Mizuno-Iijima S; Tanimoto Y; Daitoku Y; Hoshino Y; Ikawa M; Takahashi S; Sugiyama F; Yagami K
    Mamm Genome; 2014 Aug; 25(7-8):327-34. PubMed ID: 24879364
    [TBL] [Abstract][Full Text] [Related]  

  • 35.
    Liu L; Cao J; Chang Q; Xing F; Yan G; Fu L; Wang H; Ma Z; Chen X; Li Y; Li S
    Hum Gene Ther; 2019 Sep; 30(9):1079-1092. PubMed ID: 31144528
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Evaluation of CRISPR/Cas9 exon-skipping vector for choroideremia using human induced pluripotent stem cell-derived RPE.
    Iwagawa T; Masumoto H; Tabuchi H; Tani K; Conklin BR; Watanabe S
    J Gene Med; 2023 Feb; 25(2):e3464. PubMed ID: 36413603
    [TBL] [Abstract][Full Text] [Related]  

  • 37. CRISPR/Cas9-Mediated Highly Efficient Gene Targeting in Embryonic Stem Cells for Developing Gene-Manipulated Mouse Models.
    Ozawa M; Emori C; Ikawa M
    J Vis Exp; 2022 Aug; (186):. PubMed ID: 36094255
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Generation of a New Tau Knockout (tauΔex1) Line Using CRISPR/Cas9 Genome Editing in Mice.
    Tan DCS; Yao S; Ittner A; Bertz J; Ke YD; Ittner LM; Delerue F
    J Alzheimers Dis; 2018; 62(2):571-578. PubMed ID: 29480201
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Pipeline for the generation of gene knockout mice using dual sgRNA CRISPR/Cas9-mediated gene editing.
    Ghassemi B; Shamsara M; Soleimani M; Kiani J; Rassoulzadegan M
    Anal Biochem; 2019 Mar; 568():31-40. PubMed ID: 30593779
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A Convenient Cas9-based Conditional Knockout Strategy for Simultaneously Targeting Multiple Genes in Mouse.
    Chen J; Du Y; He X; Huang X; Shi YS
    Sci Rep; 2017 Mar; 7(1):517. PubMed ID: 28364122
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.