Showing 1 - 8 results of 8 for search 'Hisahide Nishio', query time: 0.09s Refine Results
  1. 1
    A novel splice variant of the human MSTN gene encodes a myostatin‐specific myostatin inhibitor

    A novel splice variant of the human MSTN gene encodes a myostatin‐specific myostatin inhibitor by Kazuhiro Maeta, Manal Farea, Hisahide Nishio, Masafumi Matsuo

    Published 2023
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  2. 2
    DBS Screening for Glycogen Storage Disease Type 1a: Detection of c.648G>T Mutation in <i>G6PC</i> by Combination of Modified Competitive Oligonucleotide Priming-PCR and Melting Curve Analysis

    DBS Screening for Glycogen Storage Disease Type 1a: Detection of c.648G>T Mutation in <i>G6PC</i> by Combination of Modified Competitive Oligonucleotide Priming-PCR and Melting Cur... by Emma Tabe Eko Niba, Yogik Onky Silvana Wijaya, Hiroyuki Awano, Naoko Taniguchi, Yasuhiro Takeshima, Hisahide Nishio, Masakazu Shinohara

    Published 2021
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  3. 3
    Sodium channels of SCNIA gene mutations in generalized epilepsy with febrile seizure plus (GEFS+) spectrum related to autism

    Sodium channels of SCNIA gene mutations in generalized epilepsy with febrile seizure plus (GEFS+) spectrum related to autism by Elisabeth Herini, Yudha Patria, Gunadi Gunadi, Surini Yusoff, Indra SAri Kusuma Harahap, Sunartini Sunartini, Sutaryo Sutaryo, Satoshi Takada, Hisahide Nishio

    Published 2010
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  4. 4
    Changes in the Incidence of Infantile Spinal Muscular Atrophy in Shikoku, Japan between 2011 and 2020

    Changes in the Incidence of Infantile Spinal Muscular Atrophy in Shikoku, Japan between 2011 and 2020 by Kentaro Okamoto, Hisahide Nishio, Takahiro Motoki, Toshihiro Jogamoto, Kaori Aibara, Yoichi Kondo, Kentaro Kawamura, Yukihiko Konishi, Chiho Tokorodani, Ritsuo Nishiuchi, Mariko Eguchi

    Published 2022
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  5. 5
    Determining the association between polymorphisms of the <em>DAT1</em> and <em>DRD4</em> genes with attention deficit hyperactivity disorder in children from Java Island

    Determining the association between polymorphisms of the <em>DAT1</em> and <em>DRD4</em> genes with attention deficit hyperactivity disorder in children from Java Island by Cempaka Thursina, Dian Kesumapramudya Nurputra, Indra Sari Kusuma Harahap, Nur Imma Fatimah Harahap, Nihayatus Sa'adah, Samekto Wibowo, Sri Sutarni, Ahmad Hamim Sadewa, Hermawan Hanjaya, Hisahide Nishio

    Published 2020
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  6. 6
    Assessment of Spinal Muscular Atrophy Carrier Status by Determining <i>SMN1</i> Copy Number Using Dried Blood Spots

    Assessment of Spinal Muscular Atrophy Carrier Status by Determining <i>SMN1</i> Copy Number Using Dried Blood Spots by Yogik Onky Silvana Wijaya, Jamiyan Purevsuren, Nur Imma Fatimah Harahap, Emma Tabe Eko Niba, Yoshihiro Bouike, Dian Kesumapramudya Nurputra, Mawaddah Ar Rochmah, Cempaka Thursina, Sunartini Hapsara, Seiji Yamaguchi, Hisahide Nishio, Masakazu Shinohara

    Published 2020
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  7. 7
    Gestational Age-Dependent Increase of Survival Motor Neuron Protein in Umbilical Cord-Derived Mesenchymal Stem Cells

    Gestational Age-Dependent Increase of Survival Motor Neuron Protein in Umbilical Cord-Derived Mesenchymal Stem Cells by Sota Iwatani, Nur Imma Fatimah Harahap, Dian Kesumapramudya Nurputra, Shinya Tairaku, Akemi Shono, Daisuke Kurokawa, Keiji Yamana, Khin Kyae Mon Thwin, Makiko Yoshida, Masami Mizobuchi, Tsubasa Koda, Kazumichi Fujioka, Mariko Taniguchi-Ikeda, Hideto Yamada, Ichiro Morioka, Kazumoto Iijima, Hisahide Nishio, Noriyuki Nishimura

    Published 2017
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  8. 8
    Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in Japan

    Spinal Muscular Atrophy: Diagnosis, Incidence, and Newborn Screening in Japan by Tomokazu Kimizu, Shinobu Ida, Kentaro Okamoto, Hiroyuki Awano, Emma Tabe Eko Niba, Yogik Onky Silvana Wijaya, Shin Okazaki, Hideki Shimomura, Tomoko Lee, Koji Tominaga, Shin Nabatame, Toshio Saito, Takashi Hamazaki, Norio Sakai, Kayoko Saito, Haruo Shintaku, Kandai Nozu, Yasuhiro Takeshima, Kazumoto Iijima, Hisahide Nishio, Masakazu Shinohara

    Published 2021
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