Reference |
---|
Kwon J, Kim M, Hwang W, Jo A, Hwang G, Jung M, et al. Extru-seq: a method for predicting genome-wide Cas9 off-target sites with advantages of both cell-based and in vitro approaches. Genome Biol. 2023;24:4 pubmed publisher
|
Pardieck J, Harb M, Sakiyama Elbert S. A transgenic mouse embryonic stem cell line for puromycin selection of V0V interneurons from heterogenous induced cultures. Stem Cell Res Ther. 2022;13:131 pubmed publisher
|
Kwon T, Ra J, Lee S, Baek I, Khim K, Lee E, et al. Precision targeting tumor cells using cancer-specific InDel mutations with CRISPR-Cas9. Proc Natl Acad Sci U S A. 2022;119: pubmed publisher
|
Hathi D, Chanswangphuwana C, Cho N, Fontana F, Maji D, Ritchey J, et al. Ablation of VLA4 in multiple myeloma cells redirects tumor spread and prolongs survival. Sci Rep. 2022;12:30 pubmed publisher
|
Akter M, Cui H, Chen Y, Ding B. Generation of two induced pluripotent stem cell lines with heterozygous and homozygous GAG deletion in TOR1A gene from a healthy hiPSC line. Stem Cell Res. 2021;56:102536 pubmed publisher
|
Gartrell J, Mellado Largarde M, Clay M, Bahrami A, Sahr N, Sykes A, et al. SLFN11 is Widely Expressed in Pediatric Sarcoma and Induces Variable Sensitization to Replicative Stress Caused By DNA-Damaging Agents. Mol Cancer Ther. 2021;20:2151-2165 pubmed publisher
|
Kim E, Kim J, Choi B, Kweon J, Park S, Lee H, et al. AWP1 Restrains the Aggressive Behavior of Breast Cancer Cells Induced by TNF-α. Front Oncol. 2021;11:631469 pubmed publisher
|
Chen Y, Sasaki Y, DiAntonio A, Milbrandt J. SARM1 is required in human derived sensory neurons for injury-induced and neurotoxic axon degeneration. Exp Neurol. 2021;:113636 pubmed publisher
|
Shin H, See J, Kweon J, Kim H, Sung G, Park S, et al. Small-molecule inhibitors of histone deacetylase improve CRISPR-based adenine base editing. Nucleic Acids Res. 2021;: pubmed publisher
|
Freibaum B, Messing J, Yang P, Kim H, Taylor J. High-fidelity reconstitution of stress granules and nucleoli in mammalian cellular lysate. J Cell Biol. 2021;220: pubmed publisher
|
Shin H, Kweon J, Kim Y. Gene Manipulation Using Fusion Guide RNAs for Cas9 and Cas12a. Methods Mol Biol. 2021;2162:185-193 pubmed publisher
|
Kang S, Lee W, An J, Lee J, Kim Y, Kim H, et al. Prediction-based highly sensitive CRISPR off-target validation using target-specific DNA enrichment. Nat Commun. 2020;11:3596 pubmed publisher
|
Munroe M, Niero E, Fok W, Vessoni A, Jeong H, Brenner K, et al. Telomere dysfunction activates p53 and represses HNF4α expression leading to impaired human hepatocyte development and function. Hepatology. 2020;: pubmed publisher
|
Mondal B, Jin H, Kallappagoudar S, Sedkov Y, Martinez T, Sentmanat M, et al. The histone deacetylase complex MiDAC regulates a neurodevelopmental gene expression program to control neurite outgrowth. elife. 2020;9: pubmed publisher
|
Zeineldin M, Federico S, Chen X, Fan Y, Xu B, Stewart E, et al. MYCN amplification and ATRX mutations are incompatible in neuroblastoma. Nat Commun. 2020;11:913 pubmed publisher
|
Nickolls A, Lee M, Espinoza D, Szczot M, Lam R, Wang Q, et al. Transcriptional Programming of Human Mechanosensory Neuron Subtypes from Pluripotent Stem Cells. Cell Rep. 2020;30:932-946.e7 pubmed publisher
|
Nagati J, Xu M, Garcia T, Comerford S, Hammer R, Garcia J. A substitution mutation in a conserved domain of mammalian acetate-dependent acetyl CoA synthetase 2 results in destabilized protein and impaired HIF-2 signaling. PLoS ONE. 2019;14:e0225105 pubmed publisher
|
Wang B, Maxwell B, Joo J, Gwon Y, Messing J, Mishra A, et al. ULK1 and ULK2 Regulate Stress Granule Disassembly Through Phosphorylation and Activation of VCP/p97. Mol Cell. 2019;74:742-757.e8 pubmed publisher
|
Niwa Y, Kanda G, Yamada R, Shi S, Sunagawa G, Ukai Tadenuma M, et al. Muscarinic Acetylcholine Receptors Chrm1 and Chrm3 Are Essential for REM Sleep. Cell Rep. 2018;24:2231-2247.e7 pubmed publisher
|
Lee J, Jeong E, Lee J, Jung M, Shin E, Kim Y, et al. Directed evolution of CRISPR-Cas9 to increase its specificity. Nat Commun. 2018;9:3048 pubmed publisher
|
Suzuki T, Asami M, Patel S, Luk L, Tsai Y, Perry A. Switchable genome editing via genetic code expansion. Sci Rep. 2018;8:10051 pubmed publisher
|
Urick M, Bell D. In vitro effects of FBXW7 mutation in serous endometrial cancer: Increased levels of potentially druggable proteins and sensitivity to SI-2 and dinaciclib. Mol Carcinog. 2018;57:1445-1457 pubmed publisher
|
Cooper M, Choi J, Staser K, Ritchey J, Devenport J, Eckardt K, et al. An "off-the-shelf" fratricide-resistant CAR-T for the treatment of T cell hematologic malignancies. Leukemia. 2018;32:1970-1983 pubmed publisher
|
Sentmanat M, Peters S, Florian C, Connelly J, Pruett Miller S. A Survey of Validation Strategies for CRISPR-Cas9 Editing. Sci Rep. 2018;8:888 pubmed publisher
|
Kweon J, Jang A, Kim D, Yang J, Yoon M, Rim Shin H, et al. Fusion guide RNAs for orthogonal gene manipulation with Cas9 and Cpf1. Nat Commun. 2017;8:1723 pubmed publisher
|
Chen Y, Kim M, Chen X, Batista P, Aoyama S, Wilusz J, et al. Sensing Self and Foreign Circular RNAs by Intron Identity. Mol Cell. 2017;67:228-238.e5 pubmed publisher
|
Kim D, Lim K, Kim S, Yoon S, Kim K, Ryu S, et al. Genome-wide target specificities of CRISPR RNA-guided programmable deaminases. Nat Biotechnol. 2017;35:475-480 pubmed publisher
|
Xu H, Iyer N, Huettner J, Sakiyama Elbert S. A puromycin selectable cell line for the enrichment of mouse embryonic stem cell-derived V3 interneurons. Stem Cell Res Ther. 2015;6:220 pubmed publisher
|
Sung Y, Jin Y, Kim S, Lee H. Generation of knockout mice using engineered nucleases. Methods. 2014;69:85-93 pubmed publisher
|
Cho S, Kim S, Kim J, Kim J. Targeted genome engineering in human cells with the Cas9 RNA-guided endonuclease. Nat Biotechnol. 2013;31:230-2 pubmed publisher
|