Saitoh Shinji

サイトウシンジ | Saitoh Shinji

Affiliation and department：
Job title： Professor
Homepage URL (1)： http://www.ncu-ped.com/index.html

Research field (1)： Fetal medicine/Pediatrics

Research keywords (4)：エピジェネティクス , 遺伝子診断 , 神経発達 , 知的障害

Research theme for competitive and other funds (28)：

2023 - 2026 The role of the recycling systems of cell surface protein on the mammalian development
2020 - 2025 Neurogenesis and its pathogenesis in the neonatal brain: an integrated understanding using advanced analytical techniques
2021 - 2024 遺伝病のthin slice撮像と人工知能による磁気共鳴画像診断法の樹立
2020 - 2024 Uncover pathomechanism of megalencephaly using brain organdies.
2020 - 2022 Endosomal recycling disorders: a novel disease entity caused by endosomal recycling defects

2017 - 2021 Clinical application of neural repair mechanisms in the brain by endogenous neural stem cells to neonatal hypoxic-ischemic encephalopathy

2017 - 2020 A study of molecular genetic analysis to hereditary conjugated hyperbilirubinemia with next-generation sequencing

2018 - 2020 がん遺伝子MYCNの神経発生での役割とその変異により起こる新規症候群の病態の解明

2016 - 2019 Comprehensive analysis of HBV genes in pediatric HBV carriers

2015 - 2019 Comprehensive next-generation sequencing analyses for therapeutic application to get fertility in congental hypogonadotropic hypogonadism males

2015 - 2018 Research for single cell expression analysis and epigenetic mechanism using RNA-FISH analyses

2016 - 2018 mTOR経路の異常により起こる巨脳症の診断法および治療法開発

2014 - 2016 Gillespie症候群の原因遺伝子同定と病態解明

2012 - 2015 Comprehensive next-generation sequencing analyses of the regulation of onset of puberty

2012 - 2014 The three-dimensional distances between the genes on each homologous chromosome in each cell as nuclear organization and genomic expression of the imprinted gene.

2011 - 2013 Recovering process from language dysfunction caused by brain damage in children using magnetoencephalography

2009 - 2012 アンジェルマン及びプラダー・ウイリー症候群の中枢神経機能障害の成因に関する研究

2007 - 2009 Remote support aimed at the acquisition of switch activities for children with spinal muscular atrophy type I

2005 - 2007 アンジェルマン症候群の遺伝学的診断法と遺伝カウンセリングの確立

2006 - 2007 Magnetoencepharographic analyses by spatial filtering for child patients with epilepsy

2005 - 2006 小児ミトコンドリア病の表現型を決定する遺伝的因子について

2005 - 2006 The validity and reliability of pupillary responses to gratings for children with cerebral visual impairment

2002 - 2004 X連鎖精神遅滞・αサラセミア症候群(ATR-X)の分子遺伝学的解析

2002 - 2003 A study of how to support for "a family with a disabled child" focusing on father's adaptation process and the relationship between parents.

2001 - 2002 ヒト15q11-q13およびマウス相同領域における刷り込み地図の作成に関する研究

2000 - 2002 Prader-Willi症候群における刷り込み遺伝子再活性化の研究

1998 - 2000 Angelman症候群患者におけるUBE3A遺伝子の変異解析とその応用

1997 - 1999 STRUCTURE-FUNCTION ANALYSIS OF DAX-1 USING Molecular analysis

Show all

Papers (425)：

Tomohiko Nakata, Jun Natsume, Hiroyuki Yamamoto, Yuji Ito, Takeshi Suzuki, Masahiro Kawaguchi, Anna Shiraki, Sumire Kumai, Fumi Sawamura, Ryosuke Suzui, et al. Underlying Disorders in Children With Infection-Related Acute Encephalopathy. Pediatric neurology. 2024. 155. 126-132
Takeshi Suzuki, Jun Natsume, Yuji Ito, Tadashi Ito, Koji Noritake, Fumie Kinoshita, Tatsuya Fukasawa, Takeshi Tsuji, Kazuya Itomi, Hirokazu Kurahashi, et al. Effect of levodopa on pathological gait in Dravet syndrome: A randomized crossover trial using three-dimensional gait analysis. Epilepsia. 2024
Midori Obayashi, Sachiko Iwata, Tomoya Okuda, Ichita Mori, Shigeharu Nakane, Yasuko Togawa, Mari Sugimoto, Takao Togawa, Kanji Muramatsu, Shinji Saitoh, et al. Antenatal Growth, Gestational Age, Birth, Enteral Feeding, and Blood Citrulline Levels in Very Low Birth Weight Infants. Nutrients. 2024. 16. 4
Tsutomu Shinohara, Jan-Renier Moonen, Yoon Hong Chun, Yannick C Lee-Yow, Kenichi Okamura, Jason M Szafron, Jordan Kaplan, Aiqin Cao, Lingli Wang, Shalina Taylor, et al. High Shear Stress Reduces ERG Causing Endothelial-Mesenchymal Transition and Pulmonary Arterial Hypertension. bioRxiv : the preprint server for biology. 2024
Kyoko Yokoi, Osuke Iwata, Satoru Kobayashi, Hideo Jinnou, Shin Kato, Shinji Saitoh, Haruo Goto. Intrauterine Inflammation, Excessive Fetal Growth and Respiratory Morbidities in Moderate-To-Late Preterm Neonates. Neonatology. 2023. 1-8

ｍore...

MISC (253)：

伊藤孝一, 武田理沙, 戸川貴夫, 杉浦時雄, 齋藤伸治. Transient Hepatitis B Surface Antigenemia after Hepatitis B Vaccination in Japan. 日本小児科学会雑誌. 2023. 127. 5
野田紗季, 大橋圭, 古山絢菜, 金千夏, 松原弘和, 伊藤嘉規, 滝藤明日香, 武内温子, 福原里美, 今枝正行, et al. 認知行動療法を行った選択性緘黙の4例. 日本小児科学会雑誌. 2022. 126. 12
鈴木美菜, 水谷優子, 林英傑, 深谷聡子, 川瀬恒哉, 津田兼之介, 岩田幸子, 久野正, 岩田欧介, 齋藤伸治. 新生児における短時間の血液中pH変化に寄与する因子の検討. 日本小児科学会雑誌. 2022. 126. 6
遠山潤, 遠山潤, 長崎啓祐, 小林悠, 赤坂紀幸, 赤坂紀幸, 大橋伯, 大橋伯, 入月浩美, 入月浩美, et al. Genetic counseling for siblings with Schaaf-Yang syndrome due to MAGEL2 pathogenic variant transmitted from father. 日本小児遺伝学会学術集会プログラム・抄録集. 2021. 44th (CD-ROM)
今川和生, 戸川貴夫, 伊藤彰悟, 伊藤孝一, 林久允, 高田英俊, 齋藤伸治. The molecular pathophysiology of neonatal cholestasis in preterm infants. 日本小児科学会雑誌. 2021. 125. 2

ｍore...

Education (1)：

1979 - 1985 Hokkaido University School of Medicine

Work history (6)：

2011/04 - 現在 Nagoya City University School of Medical Sciences Department of Pediatrics and Neonatology Professor
1995/10 - 2011/03 Hokkaido university hospital Department of Pediatrics
1993/08 - 1995/09 Case Western Reserve University Department of Genetics
1992/09 - 1993/07 Florida University College of Medicine Department of Neuroscience
1991/04 - 1992/08 Nagasaki University Department of Human Genetics

Show all

Association Membership(s) (6)：

Japanese Society of Sleep Research , Japan Epilepsy Society , Japanese Society ofHuman Genetics , Japan Society of Pediatric Genetics , Japanese Society of Child Neurology , Japanese Society of Pediatrics

※ Researcher’s information displayed in J-GLOBAL is based on the information registered in researchmap. For details, see here.

Return to Previous Page