講演・口頭発表等 - 森尾　友宏

分割表示  1,049 件中 41 - 60 件目  ／  全件表示 >>

  1. Cardinez C, Miraghazadeh B, Tanita K, da Silva E, Hoshino A, Okada S, Chand R, Asano T, Tsumura M, Yoshida K, Ohnishi H, Kato Z, Yamazaki M, Okuno Y, Miyano S, Kojima S, Ogawa S, Andrews TD, Field MA, Burgio G, Morio T, Vinuesa CG, Kanegane H, Cook M. Gain-of-Function IKBKB Mutation Causes Human Combined Immune Deficiency. 2019 Focused Meeting of the European Society of Immunodeficiencies (ESID2019) 2019.09.19 Brussels

  2. Morio T. Disorders caused by a defect in IKAROS family protein. 2019 Samsung Medeikal Center Primary Immunodeficiency Symposium 2019.07.06 Seoul

  3. Morio T. Primary immunodeficiency disorders caused by a mutation in IKAROS family gene. RIKEN IMS-JSI International Symposium on Immunology 2019 2019.06.25 Tokyo

  4. Nishimura Akira, Aoki Yuki, Ishiwata Yasuyoshi, Inoue Maiko, Ichimura Takuya, Ueyama Junichi, Matsumoto Kazuaki, Inoue Kento, Hiroki Haruka, Ono Shintaro, Okano Tsubasa, Tanaka Mari, Miyamoto Satoshi, Ashiarai Miho, Miyawaki Reiji, Yamagishi Chika, Tezuka Mari, Okawa Teppei, Hoshino Akihiro, Endo Akifumi, Yasuhara Masato, Kamiya Takahiro, Mitsuiki Noriko, Ono Toshiaki, Yanagimachi Masakatsu, Isoda Takeshi, Tomizawa Daisuke, Nagasawa Masayuki, Kajiwara Michiko, Takagi Masatoshi, Mizutani Shuki, Kanegane Hirokazu, Imai Kohsuke, Morio Tomohiro. Hematopoietic cell transplantation with reduced intensity conditioning regimen using fludarabine/busulfan and fludarabine/melphalan for primary immunodeficiency diseases . The 45th Annual Meeting of the European Society for Blood and Marrow Transplantation 2019.03.24 Frankfurt

  5. Tanita K, Cardinez C, Miraghanzadeh B, Hoshino A, Okada S, Asano T, Tsumura M, Ohnishi H, Kato Z, Morio T, Vinuesa CG, Kanegane H, Cook MC. Gain-of-function IKBKB mutation causes human combined immune deficiency. 第2回日本免疫不全・自己炎症学会総会・学術集会 2019.02.02 東京

  6. Lin HT, Kubara K, Yamazaki K, Takagi M, Naruto T, Morio T, Okumura T, Otsu M. Enhanced Selective Inhibition of KRAS Mutant Hematopoietic Progenitor Cell Expansion By MEK and Bcl-2 Inhibition . 60st American society of Hematology Annual Meeting & Exposition 2018.12.01 San Diego

  7. Isoda T, Nishimura A, Miyamoto S, Morio T, Takagi M, Murre C. Non-Coding RNA thymod transcription modulates nuclear architecture to Orchestratet-Cell fate and block T-Cell malignancies. SIOP2018 2018.11.17 Kyoto

  8. Satoshi Miyamoto, Takuya Naruto, Tomohiro Morio, Kevin Urayama, Atsushi Manabe, Masatoshi Takagi. 小児B前駆細胞性急性リンパ性白血病患者におけるTCF3のバリアント. 第60回日本小児血液・がん学会学術集会 2018.11.15 京都

  9. Okano T, Cho K, Kwamura S, Onai N, Fujii W, Kakuta S, Kanai-Azuma M, Ohteki T, Otsu M, Ariga T, Morio T. . Induced Pluripotent Stem Cell (IPSC)-Derived Macrophages Recapitulate the Pathological Features of Pulmonary Alveolar Proteinosis Caused by OAS1 Mutation.. 18th Biennial Meeting of the European Society of Immunodeficiencies (ESID2018) 2018.10.25 Lisbon

  10. Leiding J,Vogel T, Heimall J, Gignon Jadoul V, Mhaskar R, Cooper M, O`Sullivan M, Giovannini-Chami L, Thatayatikom B, Bauer C, Hamalainen S, Taskinen M, Seppanen M,Adeli M, Formankova R, Heeg M, Pozos T, Szabolcs P, Morio T, Chua I, Hague R, Hambleton S, Tangye S, Gennery A, Cunningham-Rundles C, Su H, Rao K, Milner J, Ehl S, Forbes L.. The Natural Hisory of STAT3-GOF-The Range of Clinical Manifestations and Treatment Options.. 18th Biennial Meeting of the European Society of Immunodeficiencies (ESID2018) 2018.10.25 Lisbon

  11. Yeh T. W, Okano T, Okamoto K, Yamashita M, Takashima T, Mitsuki N, Okada S, Kanegane H, Imai K, Morio T.. April Deficiency as a Cause of Common Variable Immunodeficiency. . 18th Biennial Meeting of the European Society of Immunodeficiencies (ESID2018) 2018.10.25 Lisbon

  12. Morio T, Nakajima K, Okado H.. Benzodiazepine-resistant status epilepticus in children: Alteration in GABAAR signal in children and its potential preventive measure. The World Federation of Societies of Biological Psychiatry (WFSBP). 2018.09.07 Kobe

  13. Tomohiro Morio. Overview and Updates on PID. 2018 Samsung Medeikal Center Primary Immunodeficiency Symposium 2018.07.14 Seoul,Korea

  14. Okamoto K, Shigemizu D, Okano T, Yeh TW, Takashima T, Yamashita M, Ono S, Mitsuiki N, Takagi M, Mori M, Kanegane H, Tsunoda T, Imai K, Morio T. Gwhole exome sequence analysis using the known and candidate genes for primary immunodeficiency diseases. The 2nd APSID Scientific Congress 2018.05.07 Chonquing, China

  15. Yeh TW, Okano T, Okamoto K, Yamashta M, Takashima T, Mitusiki N, Okada S, Kaneganwe H, Imai K, Morio T. APRIL deficiency a as a cause of common variable immunodeficiency. The 2nd APSID Scientific Congress 2018.05.07 Chonquing, China

  16. 中川竜一, 高澤啓, 葉姿文, 今井耕輔, 鹿島田健一, 森尾友宏. P13Kδ活性型変異により発症したと考えられる1型糖尿病の1例 . 第91回日本内分泌学会学術集会 2018.04.27 宮崎

  17. 髙澤啓, 辻敦美, 野村莉紗, 滝島茂, 和田泰格, 長崎啓祐, 伊達木澄人, 沼倉周彦, 森尾友宏, 鹿島田健一. 小児A型インスリン抵抗症の臨床像と遺伝学的背景. 第91回日本内分泌学会学術集会 2018.04.26 宮崎

  18. Tsuji-Hosokawa A, Kato T, Ogawa Y, Nomura R, Lavery R, Takasawa K, Harley V, Morio T, Takeda S, Kashimada K. SOX9 and FOXL2 Antagonistically Regulate Peptidyl Arginine Deiminase 2 (PADI2) Expression during testicular Development. 8th International Symposium on the Biology of Vertebrate Sex determination 2018.04.16 Kona

  19. Tomohiro Morio. Multi-virus specific T cell therapy for drug-resistant viral infection following hematopoietic cell transplantation. The 5th IMSUT-CGCT Symposium 2018.01.30 Tokyo

  20. 山下基, 満生紀子, 岡田賢, 井上裕三朗, 中世古知昭, Aditya K. Padhi, Kam Y Zhang, 小原收, 今井耕輔, 高木正稔, 金兼弘和, 谷内一郎, 森尾友宏. IKZF3ヘテロ結合型ミスセンス変異によるB細胞欠損症. 第1回日本免役不全・自己炎症学会総会・学術集会 2018.01.20 東京

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