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Plos One|March 6, 2018
Development of a multiple-gene-loading method by combining multi-integration system-equipped mouse artificial chromosome vector and CRISPR-Cas9Kazuhisa Honma, Satoshi Abe, Takeshi Endo, et al.
Molecular Therapy. Nucleic Acids|August 7, 2023
Treatment of CHO cells with Taxol and reversine improves micronucleation and microcell-mediated chromosome transfer efficiencyNarumi Uno, Hiroyuki Satofuka, Hitomaru Miyamoto, et al.
Stem Cell Reports|September 26, 2017
Transfer of a Mouse Artificial Chromosome into Spermatogonial Stem Cells Generates Transchromosomic MiceTakashi Shinohara, Kanako Kazuki, Narumi Ogonuki, et al.
Scientific Reports|October 9, 2024
Rejuvenation of human mesenchymal stem cells using a nonintegrative and conditionally removable Sendai virus vectorMitsuo Oshimura, Toshiaki Tabata, Narumi Uno, et al.
Scientific Reports|October 9, 2021
Construction of stable mouse artificial chromosome from native mouse chromosome 10 for generation of transchromosomic miceSatoshi Abe, Kazuhisa Honma, Akane Okada, et al.
Scientific Reports|November 11, 2017
Modification of single-nucleotide polymorphism in a fully humanized CYP3A mouse by genome editing technologySatoshi Abe, Kaoru Kobayashi, Asami Oji, et al.
Scientific Reports|August 28, 2014
Down syndrome-associated haematopoiesis abnormalities created by chromosome transfer and genome editing technologiesYasuhiro Kazuki, Yuwna Yakura, Satoshi Abe, et al.
Stem Cell Research & Therapy|March 21, 2026
Rejuvenation of mesenchymal stromal cells via partial reprogramming enables scalable generation of transcriptionally diverse MSC librariesHaochen Tu, Aoi Hosaka, Genki Hichiwa, et al.
Scientific Reports|March 15, 2023
Characterization of human anti-EpCAM antibodies for developing an antibody-drug conjugateHiroyuki Satofuka, Yayan Wang, Kyotaro Yamazaki, et al.
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