Access the full text.
Sign up today, get DeepDyve free for 14 days.
Loading next page...
/lp/wiley/dual-supramolecular-nanoparticle-vectors-enable-crispr-cas9-mediated-esAtfDhDfN
References (45)
-
Dominik Paquet, Dylan Kwart, Antonia Chen, A. Sproul, Samson Jacob, Shaun Teo, Kimberly Olsen, Andrew Gregg, S. Noggle, M. Tessier-Lavigne (2016)
Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9Nature, 533
-
Qi Liu, Kai Zhao, Chun Wang, Zhanzhan Zhang, C. Zheng, Yu Zhao, Yadan Zheng, Chaoyong Liu, Yingli An, Linqi Shi, C. Kang, Yang Liu (2018)
Multistage Delivery Nanoparticle Facilitates Efficient CRISPR/dCas9 Activation and Tumor Growth Suppression In VivoAdvanced Science, 6
-
Peng Wang, Lingmin Zhang, Wenfu Zheng, L. Cong, Zhaorong Guo, Yangzhouyun Xie, Le Wang, Rongbing Tang, Qiang Feng, Yoh Hamada, K. Gonda, Zhijian Hu, Xiaochun Wu, Xingyu Jiang (2018)
Thermo-triggered Release of CRISPR-Cas9 System by Lipid-Encapsulated Gold Nanoparticles for Tumor Therapy.Angewandte Chemie, 57 6
-
Hao Wang, Kuan-Ju Chen, Shutao Wang, M. Ohashi, K. Kamei, Jing Sun, J. Ha, Kan Liu, H. Tseng (2010)
A small library of DNA-encapsulated supramolecular nanoparticles for targeted gene delivery.Chemical communications, 46 11
-
Jin-sil Choi, Yazhen Zhu, Hongsheng Li, P. Peyda, T. Nguyen, Mo-Yuan Shen, Yanghui Yang, Jingyi Zhu, Mei Liu, Mandy Lee, Shih‐Sheng Sun, Yang Yang, Hsiao-hua Yu, Kai Chen, G. Chuang, H. Tseng (2017)
Cross-Linked Fluorescent Supramolecular Nanoparticles as Finite Tattoo Pigments with Controllable Intradermal Retention Times.ACS nano, 11 1
-
Jae‐Hyun Lee, Kuan-Ju Chen, Seung-hyun Noh, M. Garcia, Hao Wang, Wei‐Yu Lin, Heeyeong Jeong, Brian Kong, D. Stout, J. Cheon, H. Tseng (2013)
On-demand drug release system for in vivo cancer treatment through self-assembled magnetic nanoparticles.Angewandte Chemie, 52 16
-
C. Cukras, H. Wiley, B. Jeffrey, H. Sen, Amy Turriff, Yong Zeng, C. Vijayasarathy, D. Marangoni, L. Ziccardi, S. Kjellstrom, T. Park, S. Hiriyanna, J. Wright, P. Colosi, Zhijian Wu, R. Bush, L. Wei, P. Sieving (2018)
Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery.Molecular therapy : the journal of the American Society of Gene Therapy, 26 9
-
Xue Gao, Yong Tao, Yong Tao, Yong Tao, Verónica Lamas, Mingqian Huang, Wei-Hsi Yeh, B. Pan, Yujuan Hu, Yujuan Hu, J. Hu, J. Hu, J. Hu, David Thompson, David Thompson, Y. Shu, Y. Shu, Yamin Li, Hongyang Wang, Shi-ming Yang, Qiaobing Xu, D. Polley, M. Liberman, W. Kong, J. Holt, Zheng-Yi Chen, David Liu, David Liu, David Liu (2017)
Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agentsNature, 553
-
L. Swiech, Matthias Heidenreich, A. Banerjee, Naomi Habib, Yinqing Li, John Trombetta, M. Sur, Feng Zhang (2014)
In vivo interrogation of gene function in the mammalian brain using CRISPR-Cas9Nature Biotechnology, 33
-
Justin Eyquem, J. Mansilla-Soto, Theodoros Giavridis, S. Stegen, Mohamad Hamieh, K. Cunanan, Ashlesha Odak, M. Gönen, M. Sadelain (2017)
Targeting a CAR to the TRAC locus with CRISPR/Cas9 enhances tumour rejectionNature, 543
-
John Zuris, David Thompson, Y. Shu, J. Guilinger, Jeffrey Bessen, J. Hu, Morgan Maeder, J. Joung, Zheng-Yi Chen, David Liu, Z. C, Z. C (2014)
Efficient Delivery of Genome-Editing Proteins In Vitro and In VivoNature biotechnology, 33
-
Shutao Wang, Kuan-Ju Chen, Ting-Hsiang Wu, Hao Wang, Wei‐Yu Lin, M. Ohashi, P. Chiou, H. Tseng (2010)
Photothermal effects of supramolecularly assembled gold nanoparticles for the targeted treatment of cancer cells.Angewandte Chemie, 49 22
-
J. Doudna, E. Charpentier (2014)
The new frontier of genome engineering with CRISPR-Cas9Science, 346
-
Hao Wang, Kan Liu, Kuan-Ju Chen, Yujie Lu, Shutao Wang, Wei‐Yu Lin, Feng Guo, K. Kamei, Yi-Chun Chen, M. Ohashi, Mingwei Wang, M. Garcia, Xingzhong Zhao, C. Shen, H. Tseng (2010)
A rapid pathway toward a superb gene delivery system: programming structural and functional diversity into a supramolecular nanoparticle library.ACS nano, 4 10
-
F. Ran, P. Hsu, Jason Wright, Vineeta Agarwala, Vineeta Agarwala, David Scott, Feng Zhang (2013)
Genome engineering using the CRISPR-Cas9 systemNature Protocols, 8
-
V. Chu, Timm Weber, B. Wefers, W. Wurst, Sandrine Sander, K. Rajewsky, R. Kühn (2015)
Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cellsNature Biotechnology, 33
-
Hong-Xia Wang, Mingqiang Li, Ciaran Lee, S. Chakraborty, Hae-Won Kim, Gang Bao, K. Leong (2017)
CRISPR/Cas9-Based Genome Editing for Disease Modeling and Therapy: Challenges and Opportunities for Nonviral Delivery.Chemical reviews, 117 15
-
Ling Li, Linjiang Song, Xiaowei Liu, Xi Yang, Xia Li, Tao He, Ning Wang, Suleixin Yang, Chuan-jiang Yu, Tao Yin, Yanzhu Wen, Zhiyao He, Xiawei Wei, Weijun Su, Qinjie Wu, Shaohua Yao, C. Gong, Yuquan Wei (2017)
Artificial Virus Delivers CRISPR-Cas9 System for Genome Editing of Cells in Mice.ACS nano, 11 1
-
F. Jiang, J. Doudna (2017)
CRISPR-Cas9 Structures and Mechanisms.Annual review of biophysics, 46
-
P. Mora-Raimundo, D. Lozano, M. Manzano, M. Vallet‐Regí (2019)
Nanoparticles to Knockdown Osteoporosis-Related Gene and Promote Osteogenic Marker Expression for Osteoporosis TreatmentACS Nano, 13
-
Hong-Xia Wang, Ziyuan Song, Yeh-Hsing Lao, Xin Xu, Jing Gong, Du Cheng, S. Chakraborty, J. Park, Mingqiang Li, Dantong Huang, Lichen Yin, Jianjun Cheng, K. Leong (2018)
Nonviral gene editing via CRISPR/Cas9 delivery by membrane-disruptive and endosomolytic helical polypeptideProceedings of the National Academy of Sciences of the United States of America, 115
-
S. Alsaiari, S. Patil, Mram Alyami, K. Alamoudi, Fajr Aleisa, J. Merzaban, Mo Li, N. Khashab (2018)
Endosomal Escape and Delivery of CRISPR/Cas9 Genome Editing Machinery Enabled by Nanoscale Zeolitic Imidazolate Framework.Journal of the American Chemical Society, 140 1
-
Yang Liu, Juanjuan Du, Jin-sil Choi, Kuan-Ju Chen, S. Hou, Ming Yan, Wei‐Yu Lin, Ke Chen, Tracy Ro, G. Lipshutz, Lily Wu, Linqi Shi, Yunfeng Lu, H. Tseng, Hao Wang (2016)
A High-Throughput Platform for Formulating and Screening Multifunctional Nanoparticles Capable of Simultaneous Delivery of Genes and Transcription Factors.Angewandte Chemie, 55 1
-
Kathrin Schumann, Steven Lin, E. Boyer, Dimitre Simeonov, Meena Subramaniam, Rachel Gate, Genevieve Haliburton, Chun Ye, J. Bluestone, J. Doudna, A. Marson (2015)
Generation of knock-in primary human T cells using Cas9 ribonucleoproteinsProceedings of the National Academy of Sciences, 112
-
Hao Yin, Chun‐Qing Song, J. Dorkin, L. Zhu, Yingxiang Li, Qiongqiong Wu, Angela Park, Jung Yang, Sneha Suresh, Aizhan Bizhanova, Ankit Gupta, M. Bolukbasi, Stephen Walsh, R. Bogorad, G. Gao, Z. Weng, Yizhou Dong, V. Koteliansky, S. Wolfe, R. Langer, Wen Xue, Daniel Anderson (2016)
Therapeutic genome editing by combined viral and non-viral delivery of CRISPR system components in vivoNature biotechnology, 34
-
Zhijian Wu, Hongyan Yang, P. Colosi (2010)
Effect of genome size on AAV vector packaging.Molecular therapy : the journal of the American Society of Gene Therapy, 18 1
-
Ling Li, Shuo Hu, Xiaoyuan Chen (2018)
Non-viral delivery systems for CRISPR/Cas9-based genome editing: Challenges and opportunities.Biomaterials, 171
-
Yuxuan Wu, Dan Liang, Yinghua Wang, M. Bai, Wei Tang, Shi-min Bao, Zhiqiang Yan, Dangsheng Li, Jinsong Li (2013)
Correction of a genetic disease in mouse via use of CRISPR-Cas9.Cell stem cell, 13 6
-
Kuan-Ju Chen, Stephanie Wolahan, Hao Wang, Chao-Hsiung Hsu, Hsing-Wei Chang, A. Durazo, L. Hwang, Mitch Garcia, Z. Jiang, Lily Wu, Yung-Ya Lin, H. Tseng (2011)
A small MRI contrast agent library of gadolinium(III)-encapsulated supramolecular nanoparticles for improved relaxivity and sensitivity.Biomaterials, 32 8
-
Jared Carlson-Stevermer, Amr Abdeen, Lucille Kohlenberg, Madelyn Goedland, Kaivalya Molugu, Meng Lou, Krishanu Saha (2017)
Assembly of CRISPR ribonucleoproteins with biotinylated oligonucleotides via an RNA aptamer for precise gene editingNature Communications, 8
-
Alexandre Orthwein, S. Noordermeer, M. Wilson, S. Landry, Radoslav Enchev, Alana Sherker, Meagan Munro, J. Pinder, Jayme Salsman, G. Dellaire, B. Xia, M. Peter, D. Durocher (2015)
A mechanism for the suppression of homologous recombination in G1 cellsNature, 528
-
Gerald Schwank, B. Koo, Valentina Sasselli, J. Dekkers, Inha Heo, T. Demircan, Nobuo Sasaki, S. Boymans, E. Cuppen, C. Ent, E. Nieuwenhuis, J. Beekman, H. Clevers (2013)
Functional repair of CFTR by CRISPR/Cas9 in intestinal stem cell organoids of cystic fibrosis patients.Cell stem cell, 13 6
-
Hao Wang, Shutao Wang, H. Su, Kuan-Ju Chen, Amanda Armijo, Wei‐Yu Lin, Yanju Wang, Jing Sun, K. Kamei, J. Czernin, C. Radu, H. Tseng (2009)
A supramolecular approach for preparation of size-controlled nanoparticles.Angewandte Chemie, 48 24
-
A. Tantri, T. Vrabec, Andrew Cu-Unjieng, A. Frost, W. Annesley, L. Donoso (2004)
X-linked retinoschisis: a clinical and molecular genetic review.Survey of ophthalmology, 49 2
-
Gerard Rodrigues, E. Shalaev, Thomas Karami, J. Cunningham, N. Slater, Hongwen Rivers (2018)
Pharmaceutical Development of AAV-Based Gene Therapy Products for the EyePharmaceutical Research, 36
-
Kunwoo Lee, M. Conboy, Hyo Park, F. Jiang, Hyun Kim, M. DeWitt, Vanessa Mackley, K. Chang, Anirudh Rao, Colin Skinner, Tamanna Shobha, Melod Mehdipour, Hui Liu, Wen-chin Huang, F. Lan, Nicolas Bray, Song Li, J. Corn, K. Kataoka, J. Doudna, I. Conboy, N. Murthy (2017)
Nanoparticle delivery of Cas9 ribonucleoprotein and donor DNA in vivo induces homology-directed DNA repairNature biomedical engineering, 1
-
Keiichiro Suzuki, Yuji Tsunekawa, R. Hernández-Benítez, Jun Wu, Jie Zhu, Euiseok Kim, Fumiyuki Hatanaka, Mako Yamamoto, T. Araoka, Zhe Li, M. Kurita, Tomoaki Hishida, Mo Li, Emi Aizawa, Shicheng Guo, S. Chen, April Goebl, R. Soligalla, J. Qu, Tingshuai Jiang, Xin-Yuan Fu, Maryam Jafari, C. Esteban, W. Berggren, J. Lajara, E. Núñez-Delicado, P. Guillen, J. Campistol, F. Matsuzaki, Guang-Hui Liu, P. Magistretti, Kun Zhang, E. Callaway, Kang Zhang, J. Belmonte (2016)
In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integrationNature, 540
-
Wujin Sun, Wenyan Ji, Jordan Hall, Quanyin Hu, Chao Wang, Chase Beisel, Zhen Gu (2015)
Self-assembled DNA nanoclews for the efficient delivery of CRISPR-Cas9 for genome editing.Angewandte Chemie, 54 41
-
Wenhua Zhou, Haodong Cui, L. Ying, Xuefeng Yu (2018)
Enhanced Cytosolic Delivery and Release of CRISPR/Cas9 by Black Phosphorus Nanosheets for Genome Editing.Angewandte Chemie, 57 32
-
Ming Wang, John Zuris, Fantao Meng, H. Rees, Shuo Sun, Pu Deng, Yong Han, Xue Gao, Dimitra Pouli, Qi Wu, I. Georgakoudi, David Liu, Qiaobing Xu (2016)
Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticlesProceedings of the National Academy of Sciences, 113
-
E. Papapetrou, A. Schambach (2016)
Gene Insertion Into Genomic Safe Harbors for Human Gene Therapy.Molecular therapy : the journal of the American Society of Gene Therapy, 24 4
-
Xiangjun He, Chunlai Tan, Feng Wang, Yaofeng Wang, Rui Zhou, Dexuan Cui, Wenxing You, Hui Zhao, Jianwei Ren, Bo Feng (2016)
Knock-in of large reporter genes in human cells via CRISPR/Cas9-induced homology-dependent and independent DNA repairNucleic Acids Research, 44
-
Bumwhee Lee, Kunwoo Lee, Shree Panda, Rodrigo Gonzales-Rojas, Anthony Chong, V. Bugay, Hyo Park, R. Brenner, N. Murthy, Hye Lee (2018)
Nanoparticle delivery of CRISPR into the brain rescues a mouse model of fragile X syndrome from exaggerated repetitive behavioursNature Biomedical Engineering, 2
-
(2016)
34, 328; c) -
Sarah Golding, E. Rosenberg, A. Khalil, A. McEwen, M. Holmes, S. Neill, L. Povirk, K. Valerie (2004)
Double Strand Break Repair by Homologous Recombination Is Regulated by Cell Cycle-independent Signaling via ATM in Human Glioma Cells*Journal of Biological Chemistry, 279
- Publisher
- Wiley
- Copyright
- © 2020 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim
- eISSN
- 2198-3844
- DOI
- 10.1002/advs.201903432
- Publisher site
- See Article on Publisher Site
Abstract
Journal
Advanced Science – Wiley
Published: May 1, 2020
Keywords: ; ; ; ; ;