Moriya Kunihiko 森谷邦彦

… Alternative Names

森谷邦彦モリヤクニヒコ

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Researcher Number	40646999
Other IDs
Affiliation (Current)	2025: 東北大学, 医学系研究科, 大学院非常勤講師 2025: 防衛医科大学校(医学教育部医学科進学課程及び専門課程、動物実験施設、共同利用研究施設、病院並びに防衛, 小児科学, 講師
Affiliation (based on the past Project Information) *help	2024: 防衛医科大学校(医学教育部医学科進学課程及び専門課程、動物実験施設、共同利用研究施設、病院並びに防衛, 小児科学, 助教 2023 – 2024: 防衛医科大学校(医学教育部医学科進学課程及び専門課程、動物実験施設、共同利用研究施設、病院並びに防衛, 小児科学, 講師 2022: 防衛医科大学校(医学教育部医学科進学課程及び専門課程、動物実験施設、共同利用研究施設、病院並びに防衛, 小児科学, 助教 2021: 東北大学, 医学系研究科, 非常勤講師 2019 – 2020: 東北大学, 大学病院, 助教 2015: 東北大学, 大学病院, 助教
Review Section/Research Field	Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related / 0802:Biomedical structure and function and related fields / Pediatrics Except Principal Investigator Basic Section 52050:Embryonic medicine and pediatrics-related
Keywords	Principal Investigator Ⅰ型インターフェロン / NF-κB経路 / 先天性免疫調節異常症 / 自己炎症症候群 / ドミナントネガティブ効果 / 小児全身性エリテマトーデス / Type I IFN / 優性阻害効果 / RelA / 自己炎症性疾患 … More / オーダーメイド治療 / サイトカイン阻害剤 / 若年性特発性関節炎 / トランスレーショナルリサーチ / 免疫学 / シグナル伝達 / 遺伝子 / STAT1 GOF / LRBA / CTLA4 / DIRA / エクソーム解析 / JIA … More Except Principal Investigator エピジェネティクス / 免疫学的記憶 / B細胞 / 原発性免疫不全症 / 抗体産生不全症 Less

NF-κB経路とⅠ型インターフェロン産生異常による自己炎症性疾患の病態解明Principal Investigator
- Principal Investigator
  
  森谷邦彦
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  National Defense Medical College
Elucidation of human Immunological memory through the analysis of primary antibody deficiency
- Principal Investigator
  
  今井耕輔
- Project Period (FY)
  2024 – 2026
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  National Defense Medical College
Pathophysiology elucidation of NFKB related autoimmune diseasesPrincipal Investigator
- Principal Investigator
  
  Moriya Kunihiko
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  National Defense Medical College
  Tohoku University
Responsible genes and molecular pathogenesis of JIAPrincipal Investigator
- Principal Investigator
  
  Moriya Kunihiko
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Research Activity Start-up
- Review Section
  
  0802:Biomedical structure and function and related fields
- Research Institution
  Tohoku University
臍帯血コホートを用いた小児白血病多段階発癌メカニズムの解明Principal Investigator
- Principal Investigator
  
  森谷邦彦
- Project Period (FY)
  2015 – 2016
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Tohoku University

All 2022 2021 2020

All Journal Article Presentation

[Journal Article] A partial form of inherited human USP18 deficiency underlies infection and inflammation2022
- Author(s)
  Martin-Fernandez Marta、Buta Sofija、Le Voyer Tom、Li Zhi、Dynesen Lasse Toftdal、Vuillier Fran?oise、Franklin Lina、Ailal Fatima、Muglia、 Benhsaien Ibtihal、Moriya Kunihiko、Bousfiha Aziz、Casanova Jean-Laurent、Bustamante Jacinta、Bogunovic Dusan
- Journal Title
  
  Journal of Experimental Medicine
  
  Volume: 219 Issue: 4
- DOI
  10.1084/jem.20211273
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07791
[Journal Article] Case report: Cerebellar swelling and hydrocephalus in familial hemophagocytic lymphohistiocytosis2022
- Author(s)
  Yoshida Taro、Moriya Kunihiko、Oikawa Keisuke、Miura Shoko、Asakura Yoshiko、Tanifuji Sachiko、Kusano Shuji、Endo Mikiya、Akasaka Manami
- Journal Title
  
  Frontiers in Pediatrics
  
  Volume: 10 Pages: 1051623-1051623
- DOI
  10.3389/fped.2022.1051623
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07791
[Journal Article] Novel<i>POLE</i>mutations identified in patients with IMAGE-I syndrome cause aberrant subcellular localisation and protein degradation in the nucleus2022
- Author(s)
  Nakano Tomohiro、Sasahara Yoji、Kikuchi Atsuo、Moriya Kunihiko、Niizuma Hidetaka、Niihori Tetsuya、Shirota Matsuyuki、Funayama Ryo、Nakayama Keiko、Aoki Yoko、Kure Shigeo
- Journal Title
  
  Journal of Medical Genetics
  
  Volume: 59 Issue: 11 Pages: 1116-1122
- DOI
  10.1136/jmedgenet-2021-108300
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07791, KAKENHI-PROJECT-22K12241
[Journal Article] Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome2022
- Author(s)
  Irie Masahiro、Katayama Saori、Moriya Kunihiko、Niizuma Hidetaka、Suzuki Nobu、Saito-Nanjo Yuka、Onuma MasaeiIkeda Junji、Kato Motohiro、Takita Junko、Maeda Miho、Aoki Yoko、Imaizumi Masue、Sasahara Yoji
- Journal Title
  
  International Journal of Hematology
  
  Volume: 117 Issue: 4 Pages: 598
- DOI
  10.1007/s12185-022-03505-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07791, KAKENHI-PROJECT-20H00528, KAKENHI-PROJECT-20H03637, KAKENHI-PROJECT-19K08855, KAKENHI-PROJECT-21K19405, KAKENHI-PROJECT-23K07286
[Journal Article] Stage M Infantile Neuroblastoma With Involvement of Falx Cerebri: Case Report and Literature Review2022
- Author(s)
  Sai Miyu、Moriya Kunihiko、Kaino Akira、Suzuki Tasuku、Katayama Saori、Aoki Hidekazu、Sasahara Yoji
- Journal Title
  
  Journal of Pediatric Hematology/Oncology
  
  Volume: 45 Issue: 4 Pages: 220-222
- DOI
  10.1097/mph.0000000000002548
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21K07791
[Journal Article] Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents2021
- Author(s)
  Levy R, Langlais D, Rapaport F, Moriya K, Markle J, Lim AI, Ogishi M, Yang R, Pelham S, Emam M, Migaud M, Deswarte C, Habib T, Saraiva LR, Moussa EA, Guennoun A, Boisson B, Belkaya S, Martinez-Barricarte R, Rosain J, Casanova JL, Puel A.
- Journal Title
  
  J Clin Invest
  
  Volume: 131(17) Issue: 17 Pages: 677572-677590
- DOI
  10.1172/jci150143
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07791
[Journal Article] The incidence of symptomatic osteonecrosis is similar between Japanese children and children in Western countries with acute lymphoblastic leukaemia treated with a Berlin‐Frankfurt‐M?nster (BFM)95‐based protocol2021
- Author(s)
  Moriya Kunihiko、Suenobu Souichi、et al、Japan Association of Childhood Leukemia Study Group (JACLS)
- Journal Title
  
  British Journal of Haematology
  
  Volume: 196 Issue: 5 Pages: 1257-1261
- DOI
  10.1111/bjh.17988
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07822, KAKENHI-PROJECT-21K07866, KAKENHI-PROJECT-21K07791
[Journal Article] Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants2021
- Author(s)
  Totsune E, Nakano T, Moriya K, Sato D, Suzuki D, Miura A, Katayama S, Niizuma H, Kanno J, van Zelm MC, Imai K, Kanegane H, Sasahara Y, Kure S.
- Journal Title
  
  Front Immunol
  
  Volume: 12:677572 Pages: 677572-677578
- DOI
  10.3389/fimmu.2021.677572
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K23819, KAKENHI-PROJECT-21K07791
[Journal Article] Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia-telangiectasia caused by novel compound heterozygous variants in ATM2021
- Author(s)
  Sato D, Moriya K, Nakano T, Miyagawa C, Katayama S, Niizuma H, Sasahara Y, Kure S.
- Journal Title
  
  Int J Hematol.
  
  Volume: 196(5) Issue: 6 Pages: 1257-1261
- DOI
  10.1007/s12185-021-03203-w
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21K07791
[Journal Article] Impaired respiratory burst contributes to infections in PKCδ-deficient patients2021
- Author(s)
  Neehus AL, Moriya K, Ikinciogullari A, Casanova JL, Puel A, Bustamante J.
- Journal Title
  
  J Exp Med.
  
  Volume: 218(9):e20210501. Issue: 9 Pages: 677572-677590
- DOI
  10.1084/jem.20210501
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21K07791
[Journal Article] Ruxolitinib treatment of a patient with steroid-dependent severe autoimmunity due to STAT1 gain-of-function mutation2020
- Author(s)
  Moriya K, Suzuki T, Uchida N, Nakano T, Katayama S, Irie M, Rikiishi T, Niizuma H, Okada S, Imai K, Sasahara Y, Kure S
- Journal Title
  
  Int J Hematol
  
  Volume: - Issue: 2 Pages: 258-262
- DOI
  10.1007/s12185-020-02860-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07814, KAKENHI-PROJECT-19H03620, KAKENHI-PROJECT-19K23819, KAKENHI-PROJECT-18KK0228
[Journal Article] IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation2020
- Author(s)
  Nishimura Shiho、Kobayashi Yoshiyuki、Ohnishi Hidenori、Moriya Kunihiko、Tsumura Miyuki、Sakata Sonoko、Mizoguchi Yoko、Takada Hidetoshi、Kato Zenichiro、Sancho-Shimizu Vanessa、Picard Capucine、Irani Sarosh R.、Ohara Osamu、Casanova Jean-Laurent、Puel Anne、Ishikawa Nobutsune、Okada Satoshi、Kobayashi Masao
- Journal Title
  
  Journal of Clinical Immunology
  
  Volume: 41 Issue: 1 Pages: 125-135
- DOI
  10.1007/s10875-020-00885-5
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-20K08158, KAKENHI-PROJECT-19H03613, KAKENHI-PROJECT-19H03620, KAKENHI-PROJECT-18K07840, KAKENHI-PROJECT-18K07847, KAKENHI-PROJECT-18K15716, KAKENHI-PROJECT-18KK0228, KAKENHI-PROJECT-21K07791
[Journal Article] The IL1RN Mutation Creating the Most-Upstream Premature Stop Codon Is Hypomorphic Because of a Reinitiation of Translation.2020
- Author(s)
  Moriya K, Kadowaki S, Nakano T, Akarcan SE, Kutukculer N, Aksu G, Sasahara Y, Kure S, Ohnishi H, Casanova JL, Puel A, Fukao T.
- Journal Title
  
  J Clin Immunol.
  
  Volume: 40 Issue: 4 Pages: 643-645
- DOI
  10.1007/s10875-020-00770-1
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07840, KAKENHI-PROJECT-19K23819
[Presentation] NF-κB経路の異常による免疫調節障害2022
- Author(s)
  森谷　邦彦
- Organizer
  第11回中四国免疫不全症研究会
- Invited
- Data Source
  KAKENHI-PROJECT-21K07791
[Presentation] Dominant negative RelA mutation causes autoinflammatory and autoimmune disorders2022
- Author(s)
  森谷邦彦, 中野智太,本田吉孝, 園田素史, 津村弥来, 石村匡崇, 内田崇, 角田文彦, 虻川大樹, 井澤　和司, 八角高裕, 岡田賢, 笹原洋二, 呉繁夫
- Organizer
  第5回日本免疫不全・自己炎症学会総会・学術集会
- Data Source
  KAKENHI-PROJECT-21K07791
[Presentation] Dominant negative RelA mutation causes autoinflammatory and autoimmune disorders2021
- Author(s)
  森谷邦彦, 中野智太,本田吉孝, 園田素史, 津村弥来, 石村匡崇, 内田崇, 角田文彦, 虻川大樹, 井澤　和司, 八角高裕, 岡田賢, 笹原洋二, 呉繁夫
- Organizer
  日本人類遺伝学会第66回大会
- Data Source
  KAKENHI-PROJECT-21K07791
[Presentation] Infantile-onset fulminant type 1 diabetes mellitus caused by novel compound heterozygous LRBA variants2021
- Author(s)
  森谷邦彦, 戸恒恵理子, 中野智太, 佐藤大地, 片山紗乙莉, 新妻秀剛, 今井耕輔, 金兼弘和, 笹原洋二, 呉繁夫
- Organizer
  第83回日本血液学会
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] Dominant negative RelA mutation causes autoinflammatory and autoimmune disorders2021
- Author(s)
  森谷邦彦, 中野智太,本田吉孝, 園田素史, 津村弥来, 石村匡崇, 内田崇, 角田文彦, 虻川大樹, 井澤　和司, 八角高裕, 岡田賢, 笹原洋二, 呉繁夫
- Organizer
  第124回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-21K07791
[Presentation] The IL1RN mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation2021
- Author(s)
  森谷邦彦, 門脇沙織, 中野智太,笹原洋二, 呉繁夫, 大西秀典, Jean-Laurent Casanova, Anne Puel, 深尾敏幸
- Organizer
  第4回日本免疫不全・自己炎症学会総会・学術集会
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] Utility of Ruxolitinib in a Boy with Severe Autoimmunity and Chronic Mucocutaneous Candidiasis Caused by a STAT1 Gain-of-Function Mutation2020
- Author(s)
  Kunihiko Moriya
- Organizer
  第3回日本免疫不全・自己炎症学会総会・学術集会
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] Disseminated Fusarium infection within normal range of β-D glucan in a boy with aplastic anemia following sibling donor bone marrow transplantation2020
- Author(s)
  森谷　邦彦
- Organizer
  第82回日本血液学会
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] Human Inborn Errors of the NF-κB Pathway2020
- Author(s)
  Kunihiko Moriya
- Organizer
  第3回日本免疫不全・自己炎症学会総会・学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] Autosomal dominant RelA mutation causes autoinflammatory and autoimmune disorders2020
- Author(s)
  Kunihiko Moriya
- Organizer
  3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies (APSID)
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] Autosomal dominant RELA haploinsufficiency causes autoinflammatory and autoimmune disorders2020
- Author(s)
  Kunihiko Moriya
- Organizer
  3rd Scientific Congress of Asia Pacific Society for Immunodeficiencies (APSID)
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] ヨーロッパにおける男女共同参画、フランスを例にして2020
- Author(s)
  森谷　邦彦
- Organizer
  第123回日本小児科学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-19K23819
[Presentation] The IL1RN mutation creating the most-upstream premature stop codon is hypomorphic because of a reinitiation of translation2020
- Author(s)
  Kunihiko Moriya
- Organizer
  第82回日本血液学会
- Data Source
  KAKENHI-PROJECT-19K23819

1. 今井耕輔 (90332626)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
2. 磯田健志 (80815225)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
3. OKADA Satoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
4. TSUMURA Miyuki

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
5. 末延聡一

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
6. 大西秀典

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Moriya Kunihiko 森谷 邦彦

森谷 邦彦 モリヤ クニヒコ

Research Projects

Research Products

Co-Researchers

NF-κB経路とⅠ型インターフェロン産生異常による自己炎症性疾患の病態解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Elucidation of human Immunological memory through the analysis of primary antibody deficiency

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Pathophysiology elucidation of NFKB related autoimmune diseasesPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

Responsible genes and molecular pathogenesis of JIAPrincipal Investigator

Principal Investigator

Project Period (FY)

Research Category

Review Section

Research Institution

臍帯血コホートを用いた小児白血病多段階発癌メカニズムの解明Principal Investigator

Principal Investigator

Project Period (FY)

Research Category

Research Field

Research Institution

[Journal Article] A partial form of inherited human USP18 deficiency underlies infection and inflammation2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Case report: Cerebellar swelling and hydrocephalus in familial hemophagocytic lymphohistiocytosis2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Novel<i>POLE</i>mutations identified in patients with IMAGE-I syndrome cause aberrant subcellular localisation and protein degradation in the nucleus2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Stage M Infantile Neuroblastoma With Involvement of Falx Cerebri: Case Report and Literature Review2022

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] The incidence of symptomatic osteonecrosis is similar between Japanese children and children in Western countries with acute lymphoblastic leukaemia treated with a Berlin‐Frankfurt‐M?nster (BFM)95‐based protocol2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Infantile-Onset Fulminant Type 1 Diabetes Mellitus Caused by Novel Compound Heterozygous LRBA Variants2021

Author(s)

Journal Title

DOI

Data Source

[Journal Article] Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia-telangiectasia caused by novel compound heterozygous variants in ATM2021

Author(s)

Journal Title

DOI

Data Source

Moriya Kunihiko 森谷邦彦

森谷邦彦モリヤクニヒコ