K
Keisuke Okita
Researcher at Kyoto University
Publications - 115
Citations - 26472
Keisuke Okita is an academic researcher from Kyoto University. The author has contributed to research in topics: Induced pluripotent stem cell & Embryonic stem cell. The author has an hindex of 46, co-authored 110 publications receiving 24423 citations. Previous affiliations of Keisuke Okita include Kumamoto University & Hokkaido University.
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Journal ArticleDOI
Generation of retinal cells from mouse and human induced pluripotent stem cells.
Yasuhiko Hirami,Fumitaka Osakada,Kazutoshi Takahashi,Keisuke Okita,Shinya Yamanaka,Hanako Ikeda,Nagahisa Yoshimura,Masayo Takahashi +7 more
TL;DR: It is proposed that iPSCs can be induced to differentiate into retinal cells which have a possibility to be used as patient-specific donor cells for transplantation therapies.
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Correction: Corrigendum: Epigenetic regulation of the nuclear-coded GCAT and SHMT2 genes confers human age-associated mitochondrial respiration defects
Osamu Hashizume,Sakiko Ohnishi,Takayuki Mito,Akinori Shimizu,Kaori Ishikawa,Kazuto Nakada,Manabu Soda,Hiroyuki Mano,Sumie Togayachi,Hiroyuki Miyoshi,Keisuke Okita,Jun-Ichi Hayashi +11 more
TL;DR: In this article, the authors show that reprogramming of elderly fibroblasts restores age-associated mitochondrial respiration defects, indicating that these aging phenotypes are reversible and are similar to differentiation phenotypes in that both are controlled by epigenetic regulation, not by mutations in either the nuclear or the mitochondrial genome.
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Premature Termination of Reprogramming In Vivo Leads to Cancer Development through Altered Epigenetic Regulation
Kotaro Ohnishi,Kotaro Ohnishi,Katsunori Semi,Takuya Yamamoto,Masahito Shimizu,Akito Tanaka,Kanae Mitsunaga,Keisuke Okita,Kenji Osafune,Yuko Arioka,Toshiyuki Maeda,Hidenobu Soejima,Hisataka Moriwaki,Shinya Yamanaka,Knut Woltjen,Yasuhiro Yamada,Yasuhiro Yamada +16 more
TL;DR: It is demonstrated that iPSCs derived from Dox-withdrawn kidney tumor cells give rise to nonneoplastic kidney cells in mice, proving that they have not undergone irreversible genetic transformation and suggest that epigenetic regulation associated with iPSC derivation may drive development of particular types of cancer.
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Targeted Disruption of HLA Genes via CRISPR-Cas9 Generates iPSCs with Enhanced Immune Compatibility.
Huaigeng Xu,Bo Wang,Miyuki Ono,Akihiro Kagita,Kaho Fujii,Noriko Sasakawa,Noriko Sasakawa,Tatsuki Ueda,Peter Gee,Peter Gee,Misato Nishikawa,Masaki Nomura,Fumiyo Kitaoka,Tomoko Takahashi,Keisuke Okita,Yoshinori Yoshida,Shin Kaneko,Akitsu Hotta,Akitsu Hotta +18 more
TL;DR: Two genome-editing strategies for making immunocompatible donor iPSCs are shown, estimated to be immunologically compatible with >90% of the world's population, greatly facilitating iPSC-based regenerative medicine applications.
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Donor-dependent variations in hepatic differentiation from human-induced pluripotent stem cells
Masatoshi Kajiwara,Takashi Aoi,Keisuke Okita,Ryosuke Takahashi,Haruhisa Inoue,Naoya Takayama,Hiroshi Endo,Koji Eto,Junya Toguchida,Shinji Uemoto,Shinya Yamanaka +10 more
TL;DR: An improved hepatic differentiation protocol was developed and compared 28 hiPSC lines originated from various somatic cells and derived using retroviruses, Sendai viruses, or episomal plasmids and found that variations in hepatic differentiate were largely attributable to donor differences, rather than to the types of the original cells.