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.
346 related articles for article (PubMed ID: 33321292)
1. PLGA-Nanoparticles for Intracellular Delivery of the CRISPR-Complex to Elevate Fetal Globin Expression in Erythroid Cells. Cruz LJ; van Dijk T; Vepris O; Li TMWY; Schomann T; Baldazzi F; Kurita R; Nakamura Y; Grosveld F; Philipsen S; Eich C Biomaterials; 2021 Jan; 268():120580. PubMed ID: 33321292 [TBL] [Abstract][Full Text] [Related]
2. Optimization of CRISPR/Cas9 Delivery to Human Hematopoietic Stem and Progenitor Cells for Therapeutic Genomic Rearrangements. Lattanzi A; Meneghini V; Pavani G; Amor F; Ramadier S; Felix T; Antoniani C; Masson C; Alibeu O; Lee C; Porteus MH; Bao G; Amendola M; Mavilio F; Miccio A Mol Ther; 2019 Jan; 27(1):137-150. PubMed ID: 30424953 [TBL] [Abstract][Full Text] [Related]
3. CRISPR-Cas9 Editing of the Sharma A; Boelens JJ; Cancio M; Hankins JS; Bhad P; Azizy M; Lewandowski A; Zhao X; Chitnis S; Peddinti R; Zheng Y; Kapoor N; Ciceri F; Maclachlan T; Yang Y; Liu Y; Yuan J; Naumann U; Yu VWC; Stevenson SC; De Vita S; LaBelle JL N Engl J Med; 2023 Aug; 389(9):820-832. PubMed ID: 37646679 [TBL] [Abstract][Full Text] [Related]
4. Genome editing using CRISPR-Cas9 to create the HPFH genotype in HSPCs: An approach for treating sickle cell disease and β-thalassemia. Ye L; Wang J; Tan Y; Beyer AI; Xie F; Muench MO; Kan YW Proc Natl Acad Sci U S A; 2016 Sep; 113(38):10661-5. PubMed ID: 27601644 [TBL] [Abstract][Full Text] [Related]
5. Induction of fetal hemoglobin synthesis by CRISPR/Cas9-mediated editing of the human β-globin locus. Antoniani C; Meneghini V; Lattanzi A; Felix T; Romano O; Magrin E; Weber L; Pavani G; El Hoss S; Kurita R; Nakamura Y; Cradick TJ; Lundberg AS; Porteus M; Amendola M; El Nemer W; Cavazzana M; Mavilio F; Miccio A Blood; 2018 Apr; 131(17):1960-1973. PubMed ID: 29519807 [TBL] [Abstract][Full Text] [Related]
6. Cellular function reinstitution of offspring red blood cells cloned from the sickle cell disease patient blood post CRISPR genome editing. Wen J; Tao W; Hao S; Zu Y J Hematol Oncol; 2017 Jun; 10(1):119. PubMed ID: 28610635 [TBL] [Abstract][Full Text] [Related]
7. Two Distinct Approaches for CRISPR-Cas9-Mediated Gene Editing in Cryptococcus neoformans and Related Species. Wang P mSphere; 2018 Jun; 3(3):. PubMed ID: 29898980 [No Abstract] [Full Text] [Related]
8. Combined lentiviral- and RNA-mediated CRISPR/Cas9 delivery for efficient and traceable gene editing in human hematopoietic stem and progenitor cells. Yudovich D; Bäckström A; Schmiderer L; Žemaitis K; Subramaniam A; Larsson J Sci Rep; 2020 Dec; 10(1):22393. PubMed ID: 33372184 [TBL] [Abstract][Full Text] [Related]
9. CRISPR-Cas9 interrogation of a putative fetal globin repressor in human erythroid cells. Chung JE; Magis W; Vu J; Heo SJ; Wartiovaara K; Walters MC; Kurita R; Nakamura Y; Boffelli D; Martin DIK; Corn JE; DeWitt MA PLoS One; 2019; 14(1):e0208237. PubMed ID: 30645582 [TBL] [Abstract][Full Text] [Related]
10. Reactivation of γ-globin in adult β-YAC mice after ex vivo and in vivo hematopoietic stem cell genome editing. Li C; Psatha N; Sova P; Gil S; Wang H; Kim J; Kulkarni C; Valensisi C; Hawkins RD; Stamatoyannopoulos G; Lieber A Blood; 2018 Jun; 131(26):2915-2928. PubMed ID: 29789357 [TBL] [Abstract][Full Text] [Related]
11. Chemical Modification of Guide RNAs for Improved CRISPR Activity in CD34+ Human Hematopoietic Stem and Progenitor Cells. Shapiro J; Tovin A; Iancu O; Allen D; Hendel A Methods Mol Biol; 2021; 2162():37-48. PubMed ID: 32926376 [TBL] [Abstract][Full Text] [Related]
12. Development and IND-enabling studies of a novel Cas9 genome-edited autologous CD34 Katta V; O'Keefe K; Li Y; Mayuranathan T; Lazzarotto CR; Wood RK; Levine RM; Powers A; Mayberry K; Manquen G; Yao Y; Zhang J; Jang Y; Nimmagadda N; Dempsey EA; Lee G; Uchida N; Cheng Y; Fazio F; Lockey T; Meagher M; Sharma A; Tisdale JF; Zhou S; Yen JS; Weiss MJ; Tsai SQ Mol Ther; 2024 Oct; 32(10):3433-3452. PubMed ID: 39086133 [TBL] [Abstract][Full Text] [Related]
14. CRISPR/Cas9-Based Genome Editing for Disease Modeling and Therapy: Challenges and Opportunities for Nonviral Delivery. Wang HX; Li M; Lee CM; Chakraborty S; Kim HW; Bao G; Leong KW Chem Rev; 2017 Aug; 117(15):9874-9906. PubMed ID: 28640612 [TBL] [Abstract][Full Text] [Related]
15. Synthetic multi-layer nanoparticles for CRISPR-Cas9 genome editing. Tang H; Zhao X; Jiang X Adv Drug Deliv Rev; 2021 Jan; 168():55-78. PubMed ID: 32147450 [TBL] [Abstract][Full Text] [Related]
16. Gene Therapy with CRISPR/Cas9 Coming to Age for HIV Cure. Soriano V AIDS Rev; 2017; 19(3):167-172. PubMed ID: 29019352 [TBL] [Abstract][Full Text] [Related]
17. Fabrication and characterization of PLGA nanoparticles encapsulating large CRISPR-Cas9 plasmid. Jo A; Ringel-Scaia VM; McDaniel DK; Thomas CA; Zhang R; Riffle JS; Allen IC; Davis RM J Nanobiotechnology; 2020 Jan; 18(1):16. PubMed ID: 31959180 [TBL] [Abstract][Full Text] [Related]
18. Automated Good Manufacturing Practice-Compatible CRISPR-Cas9 Editing of Hematopoietic Stem and Progenitor Cells for Clinical Treatment of β-Hemoglobinopathies. Ureña-Bailén G; Block M; Grandi T; Aivazidou F; Quednau J; Krenz D; Daniel-Moreno A; Lamsfus-Calle A; Epting T; Handgretinger R; Wild S; Mezger M CRISPR J; 2023 Feb; 6(1):5-16. PubMed ID: 36662546 [TBL] [Abstract][Full Text] [Related]
19. Different Methods of Delivering CRISPR/Cas9 Into Cells. Chandrasekaran AP; Song M; Kim KS; Ramakrishna S Prog Mol Biol Transl Sci; 2018; 159():157-176. PubMed ID: 30340786 [TBL] [Abstract][Full Text] [Related]
20. Development of a CRISPR/Cas9 System for Methylococcus capsulatus Tapscott T; Guarnieri MT; Henard CA Appl Environ Microbiol; 2019 Jun; 85(11):. PubMed ID: 30926729 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]