Hasil Pencarian - Emi Qian

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  1. 1
    A New Horizon in Reproductive Research with Pluripotent Stem Cells: Successful In Vitro Gametogenesis in Rodents, Its Application to Large Animals, and Future In Vitro Reconstitution of Reproductive Organs Such as “Uteroid” and “Oviductoid”

    A New Horizon in Reproductive Research with Pluripotent Stem Cells: Successful In Vitro Gametogenesis in Rodents, Its Application to Large Animals, and Future In Vitro Reconstituti... oleh Sho Yoshimatsu, Iori Kisu, Emi Qian, Toshiaki Noce

    Diterbitkan 2022-06-01
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  2. 2
    Establishing an induced pluripotent stem cell line from neonatal common marmoset fibroblasts by an all-in-one episomal vector approach

    Establishing an induced pluripotent stem cell line from neonatal common marmoset fibroblasts by an all-in-one episomal vector approach oleh Sho Yoshimatsu, Emi Qian, Tsukika Sato, Masafumi Yamamoto, Mitsuru Ishikawa, Hideyuki Okano

    Diterbitkan 2021-05-01
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  3. 3
    Homologous Recombination-Enhancing Factors Identified by Comparative Transcriptomic Analyses of Pluripotent Stem Cell of Human and Common Marmoset

    Homologous Recombination-Enhancing Factors Identified by Comparative Transcriptomic Analyses of Pluripotent Stem Cell of Human and Common Marmoset oleh Sho Yoshimatsu, Mayutaka Nakajima, Emi Qian, Tsukasa Sanosaka, Tsukika Sato, Hideyuki Okano

    Diterbitkan 2022-01-01
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  4. 4
    Generation of a control human induced pluripotent stem cell line using the defective and persistent Sendai virus vector system

    Generation of a control human induced pluripotent stem cell line using the defective and persistent Sendai virus vector system oleh Zhi Zhou, Sho Yoshimatsu, Emi Qian, Mitsuru Ishikawa, Tsukika Sato, Manami Ohtaka, Mahito Nakanishi, Hideyuki Okano

    Diterbitkan 2021-10-01
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  5. 5
    A human induced pluripotent stem cell model from a patient with hereditary cerebral small vessel disease carrying a heterozygous R302Q mutation in HTRA1

    A human induced pluripotent stem cell model from a patient with hereditary cerebral small vessel disease carrying a heterozygous R302Q mutation in HTRA1 oleh Emi Qian, Masahiro Uemura, Hiroya Kobayashi, Shiho Nakamura, Fumiko Ozawa, Sho Yoshimatsu, Mitsuru Ishikawa, Osamu Onodera, Satoru Morimoto, Hideyuki Okano

    Diterbitkan 2023-04-01
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