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niida yo  新井田 要

ORCIDConnect your ORCID iD *help
… Alternative Names

新井田 要  ニイダ ヨウ

NIIDA Yo  新井田 要

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Researcher Number 40293344
Other IDs
External Links
Affiliation (Current) 2022: 金沢医科大学, 総合医学研究所, 教授
Affiliation (based on the past Project Information) *help 2022: 金沢医科大学, 総合医学研究所, 教授
2017 – 2018: 金沢医科大学, 総合医学研究所, 教授
2016: 金沢医科大学, 総合医学研究所, 准教授
2013: 金沢大学, 金沢医科大学, 准教授
2012: 金沢大学, 医学部, 准教授 … More
2011 – 2012: 金沢大学, 子どものこころの発達研究センター, 准教授
2010 – 2012: 金沢大学, 子どものこころの発達研究センター, 特任准教授
2007: Kanazawa University, Hospital, Lecturer
2005 – 2006: 金沢大学, 医学部附属病院, 助手 Less
Review Section/Research Field
Principal Investigator
Pediatrics / Laboratory medicine / Basic Section 52050:Embryonic medicine and pediatrics-related
Except Principal Investigator
Pediatrics / Psychiatric science / Embryonic/Neonatal medicine / Basic Section 54020:Connective tissue disease and allergy-related
Keywords
Principal Investigator
遺伝子診断 / 自閉症 / ゲノム刷り込み現象 / マイクロアレイ / X染色体 / リアルタイムPCR / DNAマイクロアレイ / リンカーPCR / 相関解析 / 酵素ミスマッチ法 … More / MLPA法 / 遺伝子診 / 遺伝子検査学 / 臨床遺伝学 / 遺伝子変異 / 遺伝子検査 / 体細胞モザイク / スプライシング変異 / CHIPS 法 / COLD PCR法 / MugCap法 / 次世代シーケンサー / CHIPS法 / 遺伝学 / 結節性硬化症 / ハプロ不全 / バイオマーカー … More
Except Principal Investigator
ヘムオキシゲナーゼ / 炎症 / 血管炎 / 腎尿細管 / 内皮細胞 / 幼児 / CD163 / ヘモグロビン / 骨髄移植 / 乳児白血病 / GVHD / 出生前診断 / 染色体異常 / CNV / DNAアレイ法 / 脳科学 / 脳磁図 / 聴覚 / 自閉症 / 言語 / ヘムオキシゲナーゼ1欠損症 / 溶血性貧血 / 血管内皮細胞 / ビリルビン代謝 / ヘムオキシゲナーゼ1欠損症、インド / 脳座標 / MRI / 脳画像 / 小児 / 凝固線溶系 / 単球 / CD 163 / ヘムオキシゲナーゼ1 / ヘム / 炎症防御 / ヒトHO-1欠損症 / HO / HO-1 / Heme omenase / Inflammation / Coagulation / fibrinolvsis system / Monnsvts / Endothelial cell / Vasculitis / Renal tubular enitherial cell / TAFRO症候群 / 多中心性Castleman病 / マルチプレックス解析 / DNAマイクロアレイ / バイオバンク Less
  • Research Projects

    (11 results)
  • Research Products

    (59 results)
  • Co-Researchers

    (37 People)
  •  結節性硬化症の超早期治療介入のための神経・精神症状重症度予測バイオマーカーの同定Principal Investigator

    • Principal Investigator
      新井田 要
    • Project Period (FY)
      2022 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 52050:Embryonic medicine and pediatrics-related
    • Research Institution
      Kanazawa Medical University
  •  Novel biomarker search of TAFRO syndrome and multicentric Castleman disease

    • Principal Investigator
      正木 康史
    • Project Period (FY)
      2022 – 2024
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Review Section
      Basic Section 54020:Connective tissue disease and allergy-related
    • Research Institution
      Kanazawa Medical University
  •  Construction of complementary genetic testing system for Mendelian genetic disease and social implementation in genetic medicinePrincipal Investigator

    • Principal Investigator
      NIIDA Yo
    • Project Period (FY)
      2016 – 2018
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Laboratory medicine
    • Research Institution
      Kanazawa Medical University
  •  The discovery of the second case of human heme oxygenase-1 deficiency: biological evidence of HO-1 enzyme

    • Principal Investigator
      KOIZUMI SHOICHI
    • Project Period (FY)
      2011 – 2013
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kanazawa University
  •  Algorithm for estimation of brain structural location from head surface shape in young children

    • Principal Investigator
      KIKUCHI Mitsuru
    • Project Period (FY)
      2011 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Psychiatric science
    • Research Institution
      Kanazawa University
  •  遺伝子検査の社会的要請に応じた簡便な遺伝子変異スクリーニング法の開発と普及Principal Investigator

    • Principal Investigator
      NIIDA Yo
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kanazawa University
  •  How far can the MLPA method and the DNA array method do the limit of a water chromosomal test in conquest

    • Principal Investigator
      OZAKI Mamoru
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Embryonic/Neonatal medicine
    • Research Institution
      Kanazawa Medical University
  •  広汎性発達障害におけるプロソディ理解力の生理学的指標の確立

    • Principal Investigator
      下道 喜代美
    • Project Period (FY)
      2010 – 2012
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Psychiatric science
    • Research Institution
      Kanazawa University
  •  Physiological importance of heme oxygenase-1 on hemopoiesis, inflammation and immunology system

    • Principal Investigator
      KOIZUMI Shoichi
    • Project Period (FY)
      2008 – 2010
    • Research Category
      Grant-in-Aid for Scientific Research (C)
    • Research Field
      Pediatrics
    • Research Institution
      Kanazawa University
  •  自閉症に関連するX染色体上の刷り込み遺伝子の同定Principal Investigator

    • Principal Investigator
      新井田 要
    • Project Period (FY)
      2005 – 2006
    • Research Category
      Grant-in-Aid for Exploratory Research
    • Research Field
      Pediatrics
    • Research Institution
      Kanazawa University
  •  Heme oxygenase-1 deficiency and failure of human defense mechanisms against generalized chronic inflammation

    • Principal Investigator
      KOIZUMI Shoichi
    • Project Period (FY)
      2005 – 2007
    • Research Category
      Grant-in-Aid for Scientific Research (B)
    • Research Field
      Pediatrics
    • Research Institution
      Kanazawa University

All 2019 2018 2017 2016 2013 2012 2011 2010 2008 2007 Other

All Journal Article Presentation Book

  • [Book] 小児神経専門医テキスト2017

    • Author(s)
      新井田 要
    • Total Pages
      12
    • Publisher
      診断と治療社
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Book] 小児内科 2017 Vol.49 増刊号2017

    • Author(s)
      新井田 要
    • Total Pages
      4
    • Publisher
      東京医学社
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Book] 週刊医学のあゆみ Vol.260 No.12 20172017

    • Author(s)
      新井田 要
    • Total Pages
      2
    • Publisher
      医歯薬出版
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Book] 皮膚科の臨床 Vol.59 No.6 2017 5月臨時増刊号2017

    • Author(s)
      新井田 要
    • Total Pages
      6
    • Publisher
      金原出版
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] A novel PHEX mutation associated with vitamin D-resistant rickets.2019

    • Author(s)
      Sako Saori、Niida Yo、Shima Kosuke Robert、Takeshita Yumie、Ishii Kiyo-aki、Takamura Toshinari
    • Journal Title

      Hum Genome Var.

      Volume: 6 Pages: 1-3

    • DOI

      10.1038/s41439-019-0040-3

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-18K08507, KAKENHI-PROJECT-16K08980, KAKENHI-PROJECT-19K08975, KAKENHI-PROJECT-16K09739
  • [Journal Article] Familial multifocal micronodular pneumocyte hyperplasia with a novel splicing mutation in TSC1: Three cases in one family2019

    • Author(s)
      Shoji Tetsuaki、Konno Satoshi、Niida Yo、Ogi Takahiro、Suzuki Masaru、Shimizu Kaoruko、Hida Yasuhiro、Kaga Kichizo、Seyama Kuniaki、Naka Tomoaki、Matsuno Yoshihiro、Nishimura Masaharu
    • Journal Title

      PLOS ONE

      Volume: 14 Pages: 0212370-0212370

    • DOI

      10.1371/journal.pone.0212370

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Autopsy case of right ventricular rhabdomyoma in tuberous sclerosis complex2019

    • Author(s)
      Kondo Takeshi、Niida Yo、Mizuguchi Masashi、Nagasaki Yasushi、Ueno Yasuhiro、Nishimura Akiyoshi
    • Journal Title

      Legal Medicine

      Volume: 36 Pages: 37-40

    • DOI

      10.1016/j.legalmed.2018.10.001

    • NAID

      120006888555

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Spinal muscular atrophy with respiratory distress type 1 associated with novel compound heterozygous mutations in <i>IGHMBP2</i> : Differential diagnosis in a case with congenital diaphragm eventration2018

    • Author(s)
      Yasui Y, Sato H, Niida Y, Kohno M
    • Journal Title

      Congenital Anomalies

      Volume: 印刷中 Issue: 1 Pages: 22-23

    • DOI

      10.1111/cga.12280

    • ISSN
      0914-3505
    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Human Malformation Syndromes of Defective <b><i>GLI</i></b>: Opposite Phenotypes of 2q14.2 (<b><i>GLI2</i></b>) and 7p14.2 (<b><i>GLI3</i></b>) Microdeletions and a GLIA/R Balance Model2018

    • Author(s)
      Niida Yo、Inoue Mika、Ozaki Mamoru、Takase Etsuko
    • Journal Title

      Cytogenetic and Genome Research

      Volume: 153 Pages: 56-65

    • DOI

      10.1159/000485227

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Diffusion tensor imaging and magnetic resonance spectroscopy in a patient with adult onset tuberous sclerosis complex.2018

    • Author(s)
      Ishikawa Hidehiro、Niwa Atsushi、Asahi Masaru、Matsuura Keita、Masuzugawa Satoshi、Niida Yo、Maeda Masayuki、Kondo Mineo、Tomimoto Hidekazu
    • Journal Title

      J Clin Neurosci.

      Volume: 48 Pages: 108-108

    • DOI

      10.1016/j.jocn.2017.10.072

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K08980, KAKENHI-PROJECT-16K15246
  • [Journal Article] B-cell-specific accumulation of inclusion bodies loaded with HLA class II molecules in patients with mucolipidosis II (I-cell disease)2018

    • Author(s)
      Yokoi Ayano、Niida Yo、Kuroda Mondo、Imi-Hashida Yoko、Toma Tomoko、Yachie Akihiro
    • Journal Title

      Pediatric Research

      Volume: 87 Pages: 1-7

    • DOI

      10.1038/s41390-018-0234-2

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Classification of Uniparental Isodisomy Patterns That Cause Autosomal Recessive Disorders: Proposed Mechanisms of Different Proportions and Parental Origin in Each Pattern2018

    • Author(s)
      Niida Y, Ozaki M, Shimizu M, Ueno K, Tanaka T
    • Journal Title

      Cytogenetic and Genome Research

      Volume: 印刷中 Pages: 137-146

    • DOI

      10.1159/000488572

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Clinical and molecular investigation of 14 Japanese patients with complete TFP deficiency: a comparison with Caucasian cases2017

    • Author(s)
      Bo Ryosuke、Yamada Kenji、Kobayashi Hironori、Jamiyan Purevsuren、Hasegawa Yuki、Taketani Takeshi、Fukuda Seiji、Hata Ikue、Niida Yo、Shigematsu Yosuke、Iijima Kazumoto、Yamaguchi Seiji
    • Journal Title

      J Hum Genet

      Volume: 62 Pages: 809-814

    • DOI

      10.1038/jhg.2017.52

    • Peer Reviewed / Open Access
    • Data Source
      KAKENHI-PROJECT-15K09593, KAKENHI-PROJECT-16K08980, KAKENHI-PROJECT-16K21179
  • [Journal Article] Cartilage-hair hypoplasia associated with isolated hypoganglionosis: A case report2017

    • Author(s)
      Yasui Y, Kohno M, Nishida S, Shironomae T, Satomi M, Kuwahara T, Takahashi S, Niida Y.
    • Journal Title

      Congenital Anomalies

      Volume: 57 Issue: 1 Pages: 32-34

    • DOI

      10.1111/cga.12175

    • NAID

      130008142330

    • ISSN
      0914-3505
    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] A Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome with a <i>KAT6B</i> 10-base pair palindromic duplication: A recurrent mutation causing a severe phenotype mixed with genitopatellar syndrome2017

    • Author(s)
      Niida Y, Mitani Y, Kuroda M, Yokoi A, Nakagawa H, Kato A.
    • Journal Title

      Congenital Anomalies

      Volume: 57 Issue: 3 Pages: 86-88

    • DOI

      10.1111/cga.12196

    • NAID

      130008142355

    • ISSN
      0914-3505
    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Reply to:Uniparental disomy of chromosome 1 unmasks recessive mutations of PPT1 in a boy with neuronal ceroid lipofuscinosis type 1.2017

    • Author(s)
      Niida Y, Yokoi A, Kuroda M, Mitani Y, Nakagawa H, Ozaki M.
    • Journal Title

      Brain Dev.

      Volume: 39 Pages: 184-185

    • DOI

      10.1016/j.braindev.2016.08.009

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] A novel frameshift mutation in the <i>TRPS1</i> gene caused Tricho-rhino-phalangeal syndrome type I and III in a Japanese family2016

    • Author(s)
      Itoh M, Kittaka Y, Niida Y, Saikawa Y.
    • Journal Title

      Clin Pediatr Endocrinol

      Volume: 25 Issue: 3 Pages: 115-118

    • DOI

      10.1297/cpe.25.115

    • NAID

      130005165828

    • ISSN
      0918-5739, 1347-7358
    • Language
      English
    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Angelman Syndrome Caused by Chromosomal Rearrangements: A Case Report of 46,XX,+der(13)t(13;15)(q14.1;q12)mat,-15 with an Atypical Phenotype and Review of the Literature.2016

    • Author(s)
      Niida Y, Sato H, Ozaki M, Itoh M, Ikeno K, Takase E.
    • Journal Title

      Cytogenet Genome Res.

      Volume: 149 Pages: 247-257

    • DOI

      10.1159/000450847

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] A girl with infantile neuronal ceroid lipofuscinosis caused by novel PPT1 mutation and paternal uniparental isodisomy of chromosome 1.2016

    • Author(s)
      Niida Y, Yokoi A, Kuroda M, Mitani Y, Nakagawa H, Ozaki M.
    • Journal Title

      Brain Dev.

      Volume: 38 Pages: 674-677

    • DOI

      10.1016/j.braindev.2016.01.004

    • Peer Reviewed / Acknowledgement Compliant
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Journal Article] Mutational analysis of TSC1 and TSC2 in Japanese patients with tuberous sclerosis complex revealed higher incidence of TSC1 patients than previously reported2013

    • Author(s)
      Niida Y, Wakisaka A, Tsuji T, Yamada H, Kuroda M, Mitani Y, Okumura A, Yokoi A.
    • Journal Title

      J Hum Genet

      Volume: Epub ahead of print

    • DOI

      10.1038/jhg.2013.3

    • NAID

      10031169423

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] An infant with recurrent convulsive seizures of 3 weeks duration : Questions2013

    • Author(s)
      Shimizu M
    • Journal Title

      Pediatr Nephrol published online

      Volume: 13

    • DOI

      10.1007/s00467-013-2615-4

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591531
  • [Journal Article] Anterior prefrontal hemodynamic connectivity in conscious 3- to 7-year-old children with typical development and autism spectrum disorder2013

    • Author(s)
      Kikuchi, M., Yoshimura, Y., Shitamichi, K., Ueno, S., et al., Remijn, G.B., Takahashi, T., Suzuki, M., Higashida, H., Minabe, Y.
    • Journal Title

      PLOS ONE.

      Volume: 8 Pages: 56087-56087

    • DOI

      10.1371/journal.pone.0056087

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591276, KAKENHI-PROJECT-23591697, KAKENHI-PROJECT-24390282, KAKENHI-PROJECT-24659541, KAKENHI-PROJECT-25293248
  • [Journal Article] A custom magnetoencephalography device reveals brain connectivity and high reading/decoding ability in children with autism2013

    • Author(s)
      Kikuchi, M., Yoshimura, Y., Shitamichi, K., Ueno, S., et al., Remijn, G.B., Takahashi, T., Suzuki, M., Higashida, H., Minabe, Y.
    • Journal Title

      Sci Rep

      Volume: 3 Pages: 1139-1139

    • DOI

      10.1038/srep01139

    • NAID

      120005821068

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591276, KAKENHI-PROJECT-23591697, KAKENHI-PROJECT-24659541, KAKENHI-PROJECT-25293248
  • [Journal Article] Paternal uniparental isodisomy of chromosome 22 in a patient with metachromatic leukodystrophy2012

    • Author(s)
      Niida Y, Kuroda M, Mitani Y, Yokoi A, Ozaki M
    • Journal Title

      J Hum Genet

      Volume: 57 Pages: 687-90

    • DOI

      10.1038/jhg.2012.97

    • NAID

      10031122251

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis2012

    • Author(s)
      Niida Y, Kuroda M, Mitani Y, Okumura A, Yokoi A
    • Journal Title

      Mol Genet Metab(3)

      Volume: 107 Pages: 580-5

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] Applying and testing the conveniently optimized enzyme mismatch cleavage method to clinical DNA diagnosis2012

    • Author(s)
      Niida Y
    • Journal Title

      Mol Genet Metab

      Volume: 107 Pages: 580-5

    • DOI

      10.1016/j.ymgme.2012.09.008

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] A case of acute encephalopathy with hemophagocytic lymphoh istiocytosis and clonal T-cell expansion2012

    • Author(s)
      Wada T, Nishiura K, Kuroda M, Asai E, Vu QV, Toma T, Niida Y, Yachie A
    • Journal Title

      Brain Dev

      Volume: 34 Pages: 376-379

    • DOI

      10.1016/j.braindev.2011.07.005

    • NAID

      10031050761

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] Birt-Hogg-Dube症候群の姉弟例2011

    • Author(s)
      中川研, 北楯祥子, 長内和弘, 栂博久, 新井田要
    • Journal Title

      臨床放射線

      Volume: 56(1) Pages: 133-137

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] Vascular-type Ehlers-Danlos syndrome presenting as recurrent compartment syndrome2011

    • Author(s)
      Yoshimura Y, Nishijima C, Ikeda Kikeda K, Niida Y, Inaoki M.
    • Journal Title

      Eur J Dermatol

      Volume: 21 Pages: 1022-3

    • DOI

      10.1684/ejd.2011.1542

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] Birt-Hogg-Dube症候群の姉弟例2011

    • Author(s)
      中川研, 北楯祥子, 齋藤雅俊, 藤本由貴, 小島好司, 及川卓, 土原一貴, 井口晶晴, 黄寿正, 長内和弘, 栂博久, 新井田要
    • Journal Title

      臨床放射線

      Volume: 56 Pages: 133-137

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Journal Article] Long-term follow-up of a case of hypomagnesemia with secondary hypocalcemia caused by novel TRPM6 mutation

    • Author(s)
      Shimizu, M., Niida, Y., Koizumi, S., Yachie, A.
    • Journal Title

      Pediatric Nephrology

      Volume: (in press)

    • Peer Reviewed
    • Data Source
      KAKENHI-PROJECT-23591531
  • [Presentation] がん遺伝子パネル検査 NCC Oncopanel Pilot study2018

    • Author(s)
      新井田 要
    • Organizer
      第38回北陸臨床遺伝研究会
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] Mutational Analysis of TSC1 and TSC2 in Japanese Patients with Tuberous Sclerosis Complex2018

    • Author(s)
      Yo NIIDA, Hiroki Ura, Sumihito Togi, Mamoru Ozaki
    • Organizer
      International TSC Research Conference 2018
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] 結節性硬化症の遺伝子診断の問題点と意義2018

    • Author(s)
      新井田要
    • Organizer
      第60回日本小児神経学会
    • Invited
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] Mutational Analysis of TSC1 and TSC2 in Japanese Patients with Tuberous Sclerosis Complex2017

    • Author(s)
      Niida Y, Ozaki M
    • Organizer
      14th Asian and Oceanian Congress of Child Neurology (AOCCN 2017)
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] 診療連携における遺伝科(遺伝診療部)の役割 ~ 遺伝性出血性末梢血管拡張症(オスラー病)の事例を通じて考える ~2017

    • Author(s)
      新井田 要
    • Organizer
      第56回日本鼻科学会総会
    • Invited
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] 塗抹標本とは異なる方法で作成した口腔粘膜細胞標本スライドにFISH法を行った染色体モザイクの2症例2017

    • Author(s)
      尾崎 守、新井田 要
    • Organizer
      第62回日本人類遺伝学会大会
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] 常染色体劣性遺伝性疾患発症の原因となる片親性イソダイソミーの分類2017

    • Author(s)
      新井田 要
    • Organizer
      第59回日本小児神経学会学術集会
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] 日本人結節性硬化症患者のTSC遺伝子解析2016

    • Author(s)
      新井田 要
    • Organizer
      第58回日本小児神経学会学術集会
    • Place of Presentation
      京王プラザホテル(東京都新宿区)
    • Year and Date
      2016-06-03
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] Mutational Analysis of TSC1 and TSC2 in Japanese Patients with Tuberous Sclerosis Complex Revealed Higher Incidence of TSC1 Patients than Previously Reported and unique TSC1 mutational pool2016

    • Author(s)
      Yo NIIDA, Mamoru Ozaki, Akiko Wakisaka, Takanori Tsuji, Mondo Kuroda, Yusuke Mitani and Ayano Yokoi
    • Organizer
      The 13th International Congress of Human Genetics
    • Place of Presentation
      国立京都国際会館(京都府京都市)
    • Year and Date
      2016-04-03
    • Int'l Joint Research
    • Data Source
      KAKENHI-PROJECT-16K08980
  • [Presentation] 父親由来片親性ダイソミーにより発症した後期乳児型異染性白質ジストロフィ-の一例2012

    • Author(s)
      新井田要(4) 池野郁、横井彩乃、三谷裕介、黒田文人、, 黒田文人,三谷裕介,横井彩乃,池野郁
    • Organizer
      第54回日本小児神経学会
    • Place of Presentation
      ロイトン札幌(北海道)
    • Year and Date
      2012-05-17
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] 新生児期よりdysostosis multiplexを呈し、I-cell病と診断された1例2012

    • Author(s)
      池野郁、横井彩乃、三谷裕介、黒田文人、, 黒田文人,三谷裕介,横井彩乃,池野郁.父親由来片親性ダイソミーにより発症した後期乳児型異染性白質ジストロフィ-の一例,第54回日本小児神経学会,2012年5月17日,ロイトン札幌(北海道)新井田要
    • Organizer
      第61回日本小児神経学会北陸地方会
    • Place of Presentation
      金沢駅西健康ホール(石川県)
    • Year and Date
      2012-02-05
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] 遺伝子検査におけるアレル発現テストの意義について2012

    • Author(s)
      新井田要、伊藤順庸、高瀬悦子、尾崎守、黒田文人、三谷裕介
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      京王プラザホテル(東京都)
    • Year and Date
      2012-10-26
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] 母由来7番染色体部分片親性ダイソミーにより発症した遠位尿細管性アシドーシスの1例2012

    • Author(s)
      新井田要, 高瀬悦子,尾崎守,黒田文人,三谷裕介,上野和之,清水正樹
    • Organizer
      第33回北陸臨床遺伝研究会
    • Place of Presentation
      福井商工会議所ビル(福井県)
    • Year and Date
      2012-11-23
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] MAP7D2 (Microtuble-associated protein 7 domain containing 2)はヒトX染色体上の母性刷り込み遺伝子である2011

    • Author(s)
      新井田要
    • Organizer
      第56回日本人類遺伝学会
    • Place of Presentation
      幕張メッセ(千葉県)
    • Year and Date
      2011-11-11
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] Only Dendritic Cells, but Not Lymphocytes, Acquired Tolerogenicity by PUVA-Treatment by Upregulation of Indoleamine 2,3-Dioxygenase (IDO)2011

    • Author(s)
      Hideaki Maeba, Rie Kuroda, Yo Niida, Shintaro Mase, Raita Araki, Toshihiro Fujiki, Akihiro Yachie, Shoichi Koizumi, Ryosei Nishimura
    • Organizer
      54th Annual Meeting of the American Society of Hematology (ASH)
    • Place of Presentation
      San Diego Convention Center (USA)
    • Data Source
      KAKENHI-PROJECT-23591531
  • [Presentation] コラーゲン異常症の遺伝子診断:CHIPSの応2011

    • Author(s)
      新井田要
    • Organizer
      第59回日本小児神経学会北陸地方会
    • Place of Presentation
      金沢駅西健康ホール(石川県)
    • Year and Date
      2011-02-06
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] コラーゲン異常症の遺伝子診断:CHIPSの応用2011

    • Author(s)
      新井田要
    • Organizer
      日本小児神経学会北陸地方会
    • Place of Presentation
      金沢駅西健康ホール(石川県)
    • Year and Date
      2011-02-06
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] 日本人結節性硬化症患者のTSC遺伝子解析2011

    • Author(s)
      新井田要(7), 黒田文人, 脇坂晃子, 辻隆範
    • Organizer
      第53回日本小児神経学会
    • Place of Presentation
      パシフィコ横浜(神奈川県)
    • Year and Date
      2011-05-27
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] MAP7D2はヒトX染色体上の母性刷り込み遺伝子である2011

    • Author(s)
      新井田要
    • Organizer
      第56回日本人類遺伝学会
    • Place of Presentation
      幕張メッセ(千葉県)
    • Year and Date
      2011-11-11
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] 金沢医科大学病院遺伝子医療センターの2009年度の活動について2010

    • Author(s)
      新井田要
    • Organizer
      第55回日本人類遺伝学会
    • Place of Presentation
      大宮ソニックシティ(埼玉県)
    • Year and Date
      2010-10-28
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] Donor Bone Marrow Derived IL-17 Expressing Cells Exacerbate Chronic Graft-Versus-Host Disease in a Murine Bone Marrow Transplantation2008

    • Author(s)
      Rie Kuroda, Ryosei Nishimura, Katsuaki Sato, Hideaki Maeba, Kazuhito Naka, Yo Niida, Raita Araki, Yoichiro Iwakura, Shoichi Koizumi, Akihiro Yachie
    • Organizer
      51st annual meeting of the American Society of Hematology.
    • Place of Presentation
      San Francisco Convention Center, USA
    • Year and Date
      2008-12-05
    • Data Source
      KAKENHI-PROJECT-20591275
  • [Presentation] Donor bone marrow derived IL-17 expressing cells exacerbate chronic graft-versus-host disease in a murine bone marrow transplantation.2008

    • Author(s)
      Kuroda R, Nishimura R, Sato K, Maeba H, Naka K, Niida Y, Araki R, Iwakura Y, Koizumi S, Yachie A
    • Organizer
      American Society of Hematology
    • Place of Presentation
      San Francisco
    • Data Source
      KAKENHI-PROJECT-20591275
  • [Presentation] Heme oxygenase (HO)-1 and hematopoiesis : a lesson from the first human case of HO-1 deficiency2007

    • Author(s)
      Koizumi, S., Yachie, A., Kasahara, Y., Saikawa, Y., Niida, Y., Yoma, T., Ohta, Ka., Ohta, Ku
    • Organizer
      36th Annual Scientific Meeting of the ISEH-Society for Hematology and Stem Cells
    • Place of Presentation
      Hamburg, Germany
    • Description
      「研究成果報告書概要(欧文)」より
    • Data Source
      KAKENHI-PROJECT-17390298
  • [Presentation] Heme oxygenase(HO)-1 and hematopoiesis: a lesson from the first human case of HO-1 deficiency.2007

    • Author(s)
      Koizumi S, Yachie A, Kasahara Y, Saikawa Y, Niida Y, Yoma T, Ohta Ka, Ohta ku
    • Organizer
      36th Annual Scientific Meeting of the ISEH-Society for Hematology and Stem Cells
    • Place of Presentation
      Hamburg, Germany
    • Description
      「研究成果報告書概要(和文)」より
    • Data Source
      KAKENHI-PROJECT-17390298
  • [Presentation] PUVA-treated dendritic cells have strong tolerogenic function by upregulation of IDO.

    • Author(s)
      Maeba H, Kuroda R, Niida Y, Araki R, Mase S, Fujiki T, Koizumi S, Yachie A, Nishimura R
    • Organizer
      第73回日本血液学会
    • Place of Presentation
      名古屋国際会議場(愛知県)
    • Data Source
      KAKENHI-PROJECT-23591531
  • [Presentation] 母由来7番染色体部分片親性ダイソミーにより発症した遠位尿細管性アシドーシスの1例

    • Author(s)
      新井田 要
    • Organizer
      第33回北陸臨床遺伝研究会
    • Place of Presentation
      福井商工会議所ビル(福井県)
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] 遺伝子検査におけるアレル発現テストの意義について

    • Author(s)
      新井田 要
    • Organizer
      第57回日本人類遺伝学会
    • Place of Presentation
      京王プラザホテル(東京都)
    • Data Source
      KAKENHI-PROJECT-22591122
  • [Presentation] 父親由来片親性ダイソミーにより発症した後期乳児型異染性白質ジストロフィ―の一例

    • Author(s)
      新井田 要
    • Organizer
      第54回日本小児神経学会
    • Place of Presentation
      ロイトン札幌(北海道)
    • Data Source
      KAKENHI-PROJECT-22591122
  • 1.  OHTA Kunio (00303280)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 2 results
  • 2.  KOIZUMI Shoichi (50019973)
    # of Collaborated Projects: 3 results
    # of Collaborated Products: 8 results
  • 3.  WADA Tatzou (30313646)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 4.  YACHIE Akihiro (40210281)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 6 results
  • 5.  NISHIMURA Ryousei (50324116)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 4 results
  • 6.  SUGIMOTO Naotoshi (80272954)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 7.  SAIKAWA Yutaka (60283107)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 2 results
  • 8.  ISHIGAKI Yasuhito (20232275)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 0 results
  • 9.  KIKUCHI Mitsuru (00377384)
    # of Collaborated Projects: 2 results
    # of Collaborated Products: 2 results
  • 10.  OZAKI Mamoru (50319068)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 11.  SHIMIZU Masaki (10401902)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 12.  SANADA Shigeru (50020029)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 13.  KASAHARA Yoshihito (30204366)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 14.  OHTA Kazuhide (20283129)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 15.  下道 喜代美 (70569475)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 16.  松井 智子 (20296792)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 17.  棟居 俊夫 (50293353)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 2 results
  • 18.  研 澄仁 (40709391)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 19.  浦 大樹 (90624958)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 20.  正木 康史 (40238895)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 21.  塚本 憲史 (10292583)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 22.  黒瀬 望 (10319048)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 23.  川端 浩 (10329401)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 24.  飯田 安保 (10337173)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 25.  三浦 勝浩 (10468738)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 26.  青木 定夫 (40242408)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 27.  山田 壮亮 (90525453)
    # of Collaborated Projects: 1 results
    # of Collaborated Products: 0 results
  • 28.  YAMADA Kenji
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 29.  ISHII Kiyoaki
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 30.  Niwa Atsushi
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 31.  Ishikawa Hidehiro
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 32.  REMIJN Gerard Bastiaan
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 33.  山口 清次
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 34.  竹下 有美枝
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 35.  冨本 秀和
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 1 results
  • 36.  吉村 優子
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results
  • 37.  上野 沙奈絵
    # of Collaborated Projects: 0 results
    # of Collaborated Products: 2 results

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