Gee P - Search Results

1

Minimizing off-Target Mutagenesis Risks Caused by Programmable Nucleases.

Ishida K, Gee P, Hotta A. Ishida K, et al. Among authors: gee p. Int J Mol Sci. 2015 Oct 16;16(10):24751-71. doi: 10.3390/ijms161024751. Int J Mol Sci. 2015. PMID: 26501275 Free PMC article. Review.

2

Efficient genomic correction methods in human iPS cells using CRISPR-Cas9 system.

Li HL, Gee P, Ishida K, Hotta A. Li HL, et al. Among authors: gee p. Methods. 2016 May 15;101:27-35. doi: 10.1016/j.ymeth.2015.10.015. Epub 2015 Oct 23. Methods. 2016. PMID: 26525194 Free article. Review.

3

Cellular Reprogramming, Genome Editing, and Alternative CRISPR Cas9 Technologies for Precise Gene Therapy of Duchenne Muscular Dystrophy.

Gee P, Xu H, Hotta A. Gee P, et al. Stem Cells Int. 2017;2017:8765154. doi: 10.1155/2017/8765154. Epub 2017 May 15. Stem Cells Int. 2017. PMID: 28607562 Free PMC article. Review.

4

Site-specific randomization of the endogenous genome by a regulatable CRISPR-Cas9 piggyBac system in human cells.

Ishida K, Xu H, Sasakawa N, Lung MSY, Kudryashev JA, Gee P, Hotta A. Ishida K, et al. Among authors: gee p. Sci Rep. 2018 Jan 10;8(1):310. doi: 10.1038/s41598-017-18568-4. Sci Rep. 2018. PMID: 29321585 Free PMC article.

5

Efficient mRNA delivery system utilizing chimeric VSVG-L7Ae virus-like particles.

Zhitnyuk Y, Gee P, Lung MSY, Sasakawa N, Xu H, Saito H, Hotta A. Zhitnyuk Y, et al. Among authors: gee p. Biochem Biophys Res Commun. 2018 Nov 10;505(4):1097-1102. doi: 10.1016/j.bbrc.2018.09.113. Epub 2018 Oct 10. Biochem Biophys Res Commun. 2018. PMID: 30316514

6

Targeted Disruption of HLA Genes via CRISPR-Cas9 Generates iPSCs with Enhanced Immune Compatibility.

Xu H, Wang B, Ono M, Kagita A, Fujii K, Sasakawa N, Ueda T, Gee P, Nishikawa M, Nomura M, Kitaoka F, Takahashi T, Okita K, Yoshida Y, Kaneko S, Hotta A. Xu H, et al. Among authors: gee p. Cell Stem Cell. 2019 Apr 4;24(4):566-578.e7. doi: 10.1016/j.stem.2019.02.005. Epub 2019 Mar 7. Cell Stem Cell. 2019. PMID: 30853558 Free article.

7

CRISPR-Cas3 induces broad and unidirectional genome editing in human cells.

Morisaka H, Yoshimi K, Okuzaki Y, Gee P, Kunihiro Y, Sonpho E, Xu H, Sasakawa N, Naito Y, Nakada S, Yamamoto T, Sano S, Hotta A, Takeda J, Mashimo T. Morisaka H, et al. Among authors: gee p. Nat Commun. 2019 Dec 6;10(1):5302. doi: 10.1038/s41467-019-13226-x. Nat Commun. 2019. PMID: 31811138 Free PMC article.

8

Extracellular nanovesicles for packaging of CRISPR-Cas9 protein and sgRNA to induce therapeutic exon skipping.

Gee P, Lung MSY, Okuzaki Y, Sasakawa N, Iguchi T, Makita Y, Hozumi H, Miura Y, Yang LF, Iwasaki M, Wang XH, Waller MA, Shirai N, Abe YO, Fujita Y, Watanabe K, Kagita A, Iwabuchi KA, Yasuda M, Xu H, Noda T, Komano J, Sakurai H, Inukai N, Hotta A. Gee P, et al. Nat Commun. 2020 Mar 13;11(1):1334. doi: 10.1038/s41467-020-14957-y. Nat Commun. 2020. PMID: 32170079 Free PMC article.

9

Efficient ssODN-Mediated Targeting by Avoiding Cellular Inhibitory RNAs through Precomplexed CRISPR-Cas9/sgRNA Ribonucleoprotein.

Kagita A, Lung MSY, Xu H, Kita Y, Sasakawa N, Iguchi T, Ono M, Wang XH, Gee P, Hotta A. Kagita A, et al. Among authors: gee p. Stem Cell Reports. 2021 Apr 13;16(4):985-996. doi: 10.1016/j.stemcr.2021.02.013. Epub 2021 Mar 11. Stem Cell Reports. 2021. PMID: 33711268 Free PMC article.

10

Optimized electroporation of CRISPR-Cas9/gRNA ribonucleoprotein complex for selection-free homologous recombination in human pluripotent stem cells.

Xu H, Kita Y, Bang U, Gee P, Hotta A. Xu H, et al. Among authors: gee p. STAR Protoc. 2021 Nov 16;2(4):100965. doi: 10.1016/j.xpro.2021.100965. eCollection 2021 Dec 17. STAR Protoc. 2021. PMID: 34825222 Free PMC article.

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