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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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Generation of retinal cells from mouse and human induced pluripotent stem cells.

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

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

TL;DR: It is demonstrated that iPSCs derived from Dox-withdrawn kidney tumor cells give rise to nonneoplastic kidney cells in mice, proving that they have not undergone irreversible genetic transformation and suggest that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.

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

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.