Kunishima Shinji 國島伸治

… Alternative Names

國島伸治クニシマシンジ

KUNISHIMA Shinji 國島伸治

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Researcher Number	60373495
Other IDs
Affiliation (Current)	2025: 岐阜医療科学大学, 保健科学部, 教授
Affiliation (based on the past Project Information) *help	2018 – 2021: 岐阜医療科学大学, 保健科学部, 教授 2015 – 2016: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), その他部局等, 室長 2013 – 2016: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), 高度診断研究部, 室長 2015: 国立病院機構名古屋医療センター, 高度診断研究部分子診断研究室, 室長 2013: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), その他部局等, 室長 … More 2013: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), 臨床研究セーター, 室長 2012 – 2013: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), 臨床研究センター, 室長 2012: 独立行政法人国立病院機構(名古屋医療センター臨床研究センター), その他部局等, その他 2011: 名古屋医療センター, 臨床研究センター, 室長 2010 – 2011: Clinical research Center, Nagoya National Hospital., 高度診断研究部, 室長 2009: Clinical research Center, Nagoya National Hospital., 高度診断研究部, 室長 2008: Clinical research Center, Nagoya National Hospital., 高度診断研究部, 室長 2007: Clinical research Center, Nagoya National Hospital., 止血血栓研究部, 室長 2005 – 2007: National Hospital Organization Nagoya Medical Center, Clinical Research Center, Chief, 止血血栓研究部, 室長 2005: National Hospital Organization Nagoya Medical Center, Clinical Research Center, Chief, 臨床研究センター・止血血栓研究部, 室長 2004: 名古屋医療センター, 臨床研究センター・止血血栓研究部, 室長 2004: 名古屋医療センター臨床研究センター, 止血血栓研究部, 室長 Less
Review Section/Research Field	Principal Investigator Hematology / Basic Section 52050:Embryonic medicine and pediatrics-related Except Principal Investigator Pediatrics / Hematology
Keywords	Principal Investigator 先天性血小板減少症 / May-Hegglin anomaly / NMMHC-IIA / MYH9異常症 / MYH9 disorders / NMMHCA / 血小板 / 細胞骨格蛋白 / Congenital thrombocytopenias / Congenital thrombocytopenia … More / Congenital platelet disorders / 血小板減少症 / 血小板機能異常症 / 先天性血小板異常症 / チューブリン / 微小管 / 巨核球 / インテグリン / 巨大血小板 / GPIIb/IIIa / 先天性巨大血小板症 … More Except Principal Investigator 先天性血小板減少症 / NMMHCA / May-Hegglin anomaly / 巣状糸球体硬化症 / ネフローゼ症候群 / myosin IIA / podocyte / 原発性免疫不全症 / アクチン架橋蛋白 / 新規治療法の開発 / 国内患者疫学調査 / 小児消化器学 / 先天異常 / 小児科 / エキソンスキップ / FLNA / Congenital thrombocytopenia / Congenital platelet disorders / MYH9 disorders / 血小板減少症 / 血小板機能異常症 / 先天性血小板異常症 / MYH9異常症 / proteinuria / NMMHC-IIA / foot process / 細胞骨格分子 / MYH9 / 細胞骨格 / FSGS / 細胞骨格タンパク / 蛋白尿 / ポドサイト / Epstein症候群 / Myosin IIA / podocytc / nephrotic syndrome / Epstein syndrome Less

Molecular mechanisms of ACTN1-macrothrombocytopeniaPrincipal Investigator
- Principal Investigator
  
  Kunishima Shinji
- Project Period (FY)
  2018 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Gihu University of Medical Science
アクチン架橋蛋白を介した免疫調節機構の解明
- Principal Investigator
  
  安冨素子
- Project Period (FY)
  2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  University of Fukui
ヒトiPSおよび新規遺伝子改変マウスを用いたネフローゼ症候群の病因解明
- Principal Investigator
  
  SEKINE Takashi
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Pediatrics
- Research Institution
  Toho University
Molecular pathogenesis of beta1 tubulin disordersPrincipal Investigator
- Principal Investigator
  
  Kunishima Shinji
- Project Period (FY)
  2014 – 2016
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  National Hospital Organization Nagoya Medical Center
Investigation of pathology and development of specific medial care system and treatment associated with FLNA deficiency
- Principal Investigator
  
  Kawai Tomoki
- Project Period (FY)
  2014 – 2015
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kyoto University
Characterization of a novel disease entity due to GPIIb/IIIa mutationsPrincipal Investigator
- Principal Investigator
  
  KUNISHIMA SHINJI
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  National Hospital Organization Nagoya Medical Center
Molecular analysis of the pathophysiology basis of nephrotic syndrome
- Principal Investigator
  
  SEKINE Takashi
- Project Period (FY)
  2011 – 2013
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Toho University
Molecular pathogenesis of MYH9 disordersPrincipal Investigator
- Principal Investigator
  
  KUNISHIMA Shinji
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  Clinical research Center, Nagoya National Hospital.
Elucidation of the mechanisms of giant platelet production in MYH9 disordersPrincipal Investigator
- Principal Investigator
  
  KUNISHIMA Shinji
- Project Period (FY)
  2006 – 2007
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  Clinical research Center, Nagoya National Hospital.
Elucidation of molecular basis of May-Hegglin anomaly and its related disordes
- Principal Investigator
  
  SAITO Hidehiko
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Hematology
- Research Institution
  National Hospital Organization Nagoya Medical Center, Clinical Research Center
Establishment of differential diagnostic method for MYH9 disorders and characterization of mechanisms of leukocyte inclusion formationPrincipal Investigator
- Principal Investigator
  
  KUNISHIMA Shinji
- Project Period (FY)
  2004 – 2005
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Hematology
- Research Institution
  National Hospital Organization Nagoya Medical Center, Clinical Research Center

[Book] 臨床に直結する血栓止血学2018
- Author(s)
  國島伸治
- Total Pages
  687
- Publisher
  中外医学社
- ISBN
  9784498125797
- Data Source
  KAKENHI-PROJECT-18K07809
[Book] 血液科研修ノート2016
- Author(s)
  國島伸治
- Total Pages
  533
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-26461413
[Book] 小児の症候群2016
- Author(s)
  國島伸治
- Total Pages
  511
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-26461413
[Book] 小児血液・腫瘍学2015
- Author(s)
  國島伸治
- Total Pages
  8
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-26461413
[Book] 小児慢性特定疾病―診断の手引き̶2015
- Author(s)
  國島伸治
- Total Pages
  7
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-26461413
[Book] Annual Review 2015 血液2015
- Author(s)
  兼松　毅　國島伸治
- Total Pages
  240
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-26461413
[Book] 血小板産生とその異常-先天性巨大血小板症- Annual Review 2014血液2014
- Author(s)
  國島伸治, (高久史麿、小澤敬也、坂田洋一、金倉譲、小島勢二編集)
- Publisher
  中外医学社, (東京)
- Data Source
  KAKENHI-PROJECT-23591429
[Book] 血小板産生とその異常-先天性巨大血小板症-Annual Review 2014 血液2014
- Author(s)
  國島伸治
- Total Pages
  240
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-23591429
[Book] 血栓・止血異常の診療2014
- Author(s)
  國島伸治
- Total Pages
  297
- Publisher
  中山書店
- Data Source
  KAKENHI-PROJECT-26461413
[Book] Epstein症候群日本臨床新領域別症候群シリーズNo22血液症候群第2版2013
- Author(s)
  國島伸治
- Publisher
  日本臨床社, (東京)
- Data Source
  KAKENHI-PROJECT-23591429
[Book] 日本臨床　新領域別症候群シリーズNo22　血液症候群第2版2013
- Author(s)
  國島伸治
- Publisher
  日本臨床社
- Data Source
  KAKENHI-PROJECT-23591429
[Book] Sebastian症候群日本臨床新領域別症候群シリーズNo22血液症候群第2版2013
- Author(s)
  國島伸治
- Publisher
  日本臨床社, (東京)
- Data Source
  KAKENHI-PROJECT-23591429
[Book] Bernard-Soulier症候群日本臨床新領域別症候群シリーズNo22血液症候群第2版2013
- Author(s)
  國島伸治
- Publisher
  日本臨床社, (東京)
- Data Source
  KAKENHI-PROJECT-23591429
[Book] Fechtner症候群日本臨床新領域別症候群シリーズNo22血液症候群第2版2013
- Author(s)
  國島伸治
- Publisher
  日本臨床社, (東京)
- Data Source
  KAKENHI-PROJECT-23591429
[Book] May-Hegglin anomaly.標本に学ぶ血液疾患症例2012
- Author(s)
  國島伸治、齋藤英彦
- Publisher
  医薬ジャーナル社, (大阪)
- Data Source
  KAKENHI-PROJECT-23591429
[Book] 先天性巨大血小板症の原因となるGPIIb/IIIa異常Annual Review 2012血液2012
- Author(s)
  國島伸治, (高久史麿、小澤敬也、坂田洋一、金倉譲、小島勢二編集)
- Publisher
  中外医学社, (東京)
- Data Source
  KAKENHI-PROJECT-23591429
[Book] Gray platelet t症候群.小児科診療(増刊号小児の症候群)(東京都)2009
- Author(s)
  國島伸治
- Total Pages
  261
- Publisher
  診断と治療社
- Data Source
  KAKENHI-PROJECT-20591161
[Book] 先天性血小板減少症:May-Hegglin n異常.新しい診断・治療のABC Cシリーズ63「血小板減少症・増多症」(池田康夫編集)(最新医学別冊)(大阪)2009
- Author(s)
  國島伸治
- Publisher
  最新医学社
- Data Source
  KAKENHI-PROJECT-20591161
[Book] Annual Review 2006 血液遺伝性血小板減少症の遺伝子異常2006
- Author(s)
  國島伸治
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-18591094
[Book] 図説血栓・止血・血管学血栓症制圧のために2005
- Author(s)
  國島伸治
- Publisher
  中外医学社
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590971
[Book] 図説血栓・止血・血管学血栓症制圧のために2005
- Author(s)
  國島伸治
- Publisher
  中外医学社
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Expanding the genetic spectrum of TUBB1- related thrombocytopenia2021
- Author(s)
  Palma-Barqueros V, Bury L, Kunishima S, Lozano ML, Rodriguez Alen A, Revilla N, Bohdan N, Padilla J, Fernandez-Perez MP, de la Morena-Barrio ME, Marin-Quilez A, Benito R, Lopez-Fernandez MF, Marcellini-Antonio S, Zamora-Canovas A, Vicente V, Martinez C, Gresele P, Bastida JM, Rivera J
- Journal Title
  
  Blood Advances
  
  Volume: 5 Issue: 24 Pages: 5453-5467
- DOI
  10.1182/bloodadvances.2020004057
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07809
[Journal Article] Novel ACTN1 variants in cases of thrombocytopenia2019
- Author(s)
  Vincenot Anne、Saultier Paul、Kunishima Shinji、Poggi Marjorie、Hurtaud‐Roux Marie‐Fran?oise、Roussel Alain、ACTN1 study coinvestigators、Schlegel Nicole、Alessi Marie‐Christine
- Journal Title
  
  Human Mutation
  
  Volume: 40 Issue: 12 Pages: 2258-2269
- DOI
  10.1002/humu.23840
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07809
[Journal Article] Congenital thrombocytopenia2018
- Author(s)
  國島伸治
- Journal Title
  
  Rinsho Ketsueki
  
  Volume: 59 Issue: 6 Pages: 764-773
- DOI
  10.11406/rinketsu.59.764
- NAID
  130007393879
- ISSN
  0485-1439, 1882-0824
- Language
  Japanese
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07809
[Journal Article] Microtubule polyglutamylation and acetylation drive microtubule dynamics critical for platelet formation2018
- Author(s)
  128.van Dijk J, Bompard G, Cau J, Kunishima S, Rabeharivelo G, Mateos-Langerak J, Cazevieille C, Cavelier P, Boizet-Bonhoure B, Delsert C, Morin N
- Journal Title
  
  BMC Biol
  
  Volume: 16 Issue: 1 Pages: 116-116
- DOI
  10.1186/s12915-018-0584-6
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07809
[Journal Article] A novel CYCS mutation in the α‐helix of the CYCS C‐terminal domain causes non‐syndromic thrombocytopenia2018
- Author(s)
  Uchiyama Yuri、Yanagisawa Kunio、Kunishima Shinji、Shiina Masaaki、Ogawa Yoshiyuki、Nakashima Mitsuko、Hirato Junko、Imagawa Eri、Fujita Atsushi、Hamanaka Kohei、Miyatake Satoko、Mitsuhashi Satomi、Takata Atsushi、Miyake Noriko、Ogata Kazuhiro、Handa Hiroshi、Matsumoto Naomichi、Mizuguchi Takeshi
- Journal Title
  
  Clinical Genetics
  
  Volume: 94 Issue: 6 Pages: 548-553
- DOI
  10.1111/cge.13423
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17K10080, KAKENHI-PROJECT-18K07809, KAKENHI-PROJECT-18K19305, KAKENHI-PROJECT-17H01539, KAKENHI-PROJECT-16H03293, KAKENHI-PROJECT-16H06254, KAKENHI-PROJECT-17H06994, KAKENHI-PROJECT-17K15630
[Journal Article] Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia2017
- Author(s)
  Sivapalaratnam S, Westbury SK, Stephens JC, Greene D, Downes K, Kelly AM, Lentaigne CE, Astle W, Huizinga EG, Nurden P, Papadia S, Peerlinck K, Penkett CJ, Perry DJ, Rougley C, Simeoni I, Stirrups K, Hart DP, Tait RC, Mumford AD, NIHR BioResources, Laffan MA, Freson K, Ouwehand WH, Kunishima S, Turro E
- Journal Title
  
  Blood
  
  Volume: 129 Issue: 4 Pages: 520-4
- DOI
  10.1182/blood-2016-08-732248
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461413
[Journal Article] Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein function2016
- Author(s)
  Oda H., Sato T., Kunishima S., Nakagawa K., Izawa K., Hiejima E., Kawai T., Yasui T., Doi H., Katamura K., Numabe H., Okamoto S., Nakase H., Hijikata A., Ohara O., Suzuki H., Morisaki H., Morisaki T., Nunoi H., Hattori S., Nishikomori R., Heike T.
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 24 Issue: 3 Pages: 408-414
- DOI
  10.1038/ejhg.2015.119
- Peer Reviewed / Acknowledgement Compliant / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15H04876, KAKENHI-PROJECT-25461143, KAKENHI-PROJECT-26860796
[Journal Article] Linkage between the mechanisms of thrombocytopenia and thrombopoiesis.2016
- Author(s)
  Eto K, Kunishima S.
- Journal Title
  
  Blood
  
  Volume: 127 Issue: 10 Pages: 1234-41
- DOI
  10.1182/blood-2015-07-607903
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-15H03005
[Journal Article] Functional characterization of a novel GFI1B mutation causing congenital macrothrombocytopenia2016
- Author(s)
  Kitamura K, Okuno Y, Yoshida K, Sanada M, Shiraishi Y, Muramatsu H, Kobayashi R, Furukawa K, Miyano S, Kojima S, Ogawa S, Kunishima S
- Journal Title
  
  J Thromb Haemost
  
  Volume: 14 Issue: 7 Pages: 1462-9
- DOI
  10.1111/jth.13350
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840
[Journal Article] Diagnostic biomarker for ACTN1 macrothrombocytopenia.2016
- Author(s)
  Kunishima S, Kitamura K, Yasutomi M, Kobayashi R.
- Journal Title
  
  Blood
  
  Volume: 126 Issue: 22 Pages: 2525-6
- DOI
  10.1182/blood-2015-08-666180
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840
[Journal Article] ACTN1 rod domain mutation associated with congenital macrothrombocytopenia.2016
- Author(s)
  Yasutomi M, Kunishima S, Okazaki S, Tanizawa A, Tsuchida S, Ohshima Y.
- Journal Title
  
  Ann Hematol
  
  Volume: 95 Issue: 1 Pages: 141-4
- DOI
  10.1007/s00277-015-2517-6
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-16K10017
[Journal Article] The first two cases of MYH9 disorders in Thailand: an international collaborative study2015
- Author(s)
  Sirachainan N, Komwilaisak P, Kitamura K, Hongeng S, Sekine T, Kunishima S
- Journal Title
  
  Ann Hematol
  
  Volume: 94 Issue: 4 Pages: 707-709
- DOI
  10.1007/s00277-014-2234-6
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840, KAKENHI-PROJECT-15H04880
[Journal Article] IL-1 alpha induces rapid enhanced platelet biogenesis through rupture of Running title: Rupture thrombopoiesis regulated by IL-1alpha murine bone marrow megakaryocytes2015
- Author(s)
  Satoshi Nishimura, Mika Nagasaki, Shinji Kunishima, Asuka Sakata, Hiroyasu Sakaguchi, Naoya Takayama, Issei Komuro, Joe Italiano Jr., Tomiko Ryu, Tsukasa Ohmori, Takashi Kadowaki, Koji Eto, Ryozo Nagai
- Journal Title
  
  Journal of cell biology
  
  Volume: 未 Issue: 3 Pages: 453-66
- DOI
  10.1083/jcb.201410052
- Peer Reviewed / Acknowledgement Compliant / Open Access
- Data Source
  KAKENHI-PROJECT-26461356, KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-15H03005, KAKENHI-PROJECT-26713013, KAKENHI-PROJECT-26000012
[Journal Article] Genotype-phenotype Correlation of the p.R1165C Mutation in the MYH9 Disorder: Report of a Japanese Pedigree.2015
- Author(s)
  Okano S, Takase M, Iseki K, Toriumi N, Kaneda M, Kunishima S.
- Journal Title
  
  J Pediatr Hematol Oncol
  
  Volume: 37 Issue: 6 Pages: e352-e355
- DOI
  10.1097/mph.0000000000000379
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-26461413
[Journal Article] ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization2015
- Author(s)
  Bottega R, Marconi C, Faleschini M, Baj G, Cagioni C, Pecci A, Pippucci T, Ramenghi, U, Pardini S, Ngu L, Baronci C, Kunishima S, Balduini CL, Seri M, Savoia A, Noris P
- Journal Title
  
  Blood
  
  Volume: 125 Issue: 5 Pages: 869-872
- DOI
  10.1182/blood-2014-08-594531
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461413
[Journal Article] Somatic mosaicism in MYH9 disorders : the need to carefully evaluate apparently healthy parents2014
- Author(s)
  Kunishima S, Kitamura K, Matsumo T, Sekine T, Saito H
- Journal Title
  
  British Journal of Haematology
  
  Volume: 165 Issue: 6 Pages: 885-887
- DOI
  10.1111/bjh.12797
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591586, KAKENHI-PROJECT-26461413, KAKENHI-PROJECT-26860840
[Journal Article] Platelet diameters in inherited thrombocytopenias: Analysis of 376 patients with all known disorders2014
- Author(s)
  Noris P, Biino G, Pecci A, Civaschi E, Savoia A, Seri M, Melazzini F, Loffredo G, Russo G, Bozzi V, Notarangelo LD, Gresele P, Heller P, Pujol-Moix N, Kunishima S, Cattaneo M, Bussel J, De Candia E, Cagioni C, Ramenghi U, Cagioni C, Fabris F, Balduini CL
- Journal Title
  
  Blood
  
  Volume: 124 Issue: 6 Pages: e4-e10
- DOI
  10.1182/blood-2014-03-564328
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461413
[Journal Article] Bernard-Soulier syndrome due to compound heterozygosity for a novel glycoprotein Ibβ mutation.2014
- Author(s)
  Sato T, Kunishima S, Shirayama R, Ichikawa S, Sakai M, Kusuhara K.
- Journal Title
  
  Acta Haematol
  
  Volume: 131 Issue: 1 Pages: 46-9
- DOI
  10.1159/000351057
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-23591559, KAKENHI-PROJECT-24591564
[Journal Article] Spectrum of the mutations in Bernard-Soulier syndrome2014
- Author(s)
  Savoia A, Kunishima S, et al
- Journal Title
  
  Hum Mut
  
  Volume: 35 Issue: 9 Pages: 1033-1045
- DOI
  10.1002/humu.22607
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461413
[Journal Article] Normal neutrophil myosin HA localization in an immunofluorescence analysis can rule out MYH9 disorders.2013
- Author(s)
  Kitamura K, Yoshida K
- Journal Title
  
  J Thromb Haemost.
  
  Volume: 11 Issue: 11 Pages: 2071-2073
- DOI
  10.1111/jth.12406
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-12J04216, KAKENHI-PROJECT-23591429
[Journal Article] Bernard-Soulier syndrome caused by a hemizygous GPIbβ mutation and 22q11.2 deletion.2013
- Author(s)
  Kunishima S, Imai T, Kobayashi R, Kato M, Ogawa S, Saito H.
- Journal Title
  
  Pediatr Int
  
  Volume: 55 Issue: 4 Pages: 434-7
- DOI
  10.1111/ped.12105
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] CAMT-iPS Cells Exhibiting Defective MPL Signaling Dysregulate Megakaryopoiesis and Erythropoiesis.2013
- Author(s)
  Shinji Hirata, Naoya Takayama,Ryoko Jono-Ohnishi, Hiroshi Endo, Sou Nakamura, Takeaki Dohda, Masanori Nishi, Yuhei Hamazaki, Ei-ichi Ishii, Shin Kaneko, Makoto Otsu, Hiromitsu Nakauchi, Shinji Kunishima, and Koji Eto.
- Journal Title
  
  J Clin Invest.
  
  Volume: 123 Issue: 9 Pages: 3802-14
- DOI
  10.1172/jci64721
- Peer Reviewed
- Data Source
  KAKENHI-PLANNED-23106004, KAKENHI-PROJECT-23591413, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-24249056, KAKENHI-PROJECT-24300160, KAKENHI-PROJECT-24659127, KAKENHI-PROJECT-25670471, KAKENHI-PROJECT-25670489
[Journal Article] Podocyte expression of nonmuscle myosin heavy chain-IIA decreases in idiopathic nephrotic syndrome, especially in focal segmental glomerulosclerosis.2013
- Author(s)
  Miura K, Kurihara H, Horita S, Chikamoto H, Hattori M, Harita Y, Tsurumi H, Kajiho Y, Sawada Y, Sasaki S, Igarashi T, Kunishima S, Sekine T.
- Journal Title
  
  Nephrol Dial Transplant.
  
  Volume: 28 Issue: 12 Pages: 2993-3003
- DOI
  10.1093/ndt/gft350
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-13J06109, KAKENHI-PROJECT-23591176, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-23591586, KAKENHI-PROJECT-24390259, KAKENHI-PROJECT-24591214, KAKENHI-PROJECT-24591569
[Journal Article] Transient macrothrombocytopenia associated with maternal-neonatal HPA-21bw incompatibility.2013
- Author(s)
  Kunishima S, Hayakawa A, Fujita K, Saito H.
- Journal Title
  
  Thromb Res
  
  Volume: 131 Issue: 6 Pages: e286-e288
- DOI
  10.1016/j.thromres.2013.05.005
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] ACTN1 Mutations Cause Congenital Macrothrombocytopenia2013
- Author(s)
  國島伸治、吉田健一
- Journal Title
  
  Am J Hum Genet
  
  Volume: 92 Issue: 3 Pages: 431-438
- DOI
  10.1016/j.ajhg.2013.01.015
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-12J04216, KAKENHI-PROJECT-23249052, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-24390242, KAKENHI-PROJECT-24390262, KAKENHI-PROJECT-24590703, KAKENHI-PROJECT-24659127, KAKENHI-PROJECT-24659458, KAKENHI-PROJECT-24659489, KAKENHI-PROJECT-24791054, KAKENHI-PROJECT-25670471, KAKENHI-PROJECT-25670489, KAKENHI-PLANNED-22134006
[Journal Article] Demonstration of novel gain-of-function mutations of αIIbβ3: association with macrothrombocytopenia and glanzmann thrombasthenia-like phenotype.2013
- Author(s)
  Kashiwagi H, Kunishima S, Kiyomizu K, Amano Y, Shimada H, Morishita M, Kanakura Y, Tomiyama Y.
- Journal Title
  
  Mol Genet Genomic Med
  
  Volume: 1 Issue: 2 Pages: 77-86
- DOI
  10.1002/mgg3.9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-24591422, KAKENHI-PROJECT-25461448
[Journal Article] Familial cases with MYH9 disorders caused by MYH9 S96L mutation2013
- Author(s)
  Murayama S, Akiyama M, Namba H, Wada Y, Ida H, Kunishima S
- Journal Title
  
  Pediatr Int
  
  Volume: 55(1) Issue: 1 Pages: 102-4
- DOI
  10.1111/j.1442-200x.2012.03619.x
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] ANKRD26-related thrombocytopenia and myeloid malignancies.2013
- Author(s)
  Noris P, Favier R, Alessi MC, Geddis AE, Kunishima S, et al.
- Journal Title
  
  Blood
  
  Volume: 122 Issue: 11 Pages: 1987-9
- DOI
  10.1182/blood-2013-04-499319
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] Establishment of mouse model of MYH9 disorders: heterozygous R702C mutation provokes macrothrombocytopenia with leukocyte inclusion bodies, renal glomerulosclerosis and hearing disability.2013
- Author(s)
  Suzuki N, Kunishima S, Ikejiri M, Maruyama S, Sone M, Takagi A, Ikawa M, Okabe M, Kojima T, Saito H, Naoe T, Matsushita T.
- Journal Title
  
  PLoS One
  
  Volume: 8 Issue: 8 Pages: 41-50
- DOI
  10.1371/journal.pone.0071187
- NAID
  120006957397
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429, KAKENHI-PLANNED-24108008, KAKENHI-PROJECT-24591421, KAKENHI-ORGANIZER-25112001, KAKENHI-PROJECT-25293129
[Journal Article] Association of a novel in-frame deletion mutation of the MYH9 gene with end-stage renal failure : case report and review of the literature2013
- Author(s)
  Ishida M, Mori Y, Ota N, Inaba T, Kunishima S
- Journal Title
  
  Clin Nephrol
  
  Volume: 80(3) Issue: 09 Pages: 218-22
- DOI
  10.5414/cn107237
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article]2012
- Author(s)
  Matsunaga T, Mutai H, Kunishima S, Namba K, Morimoto N, Shinjo Y, Arimoto Y, Kataoka Y, Shintani T, Morita N, Sugiuchi T, Masuda S, Nakano A, Taiji H, Kaga K.
- Journal Title
  
  Clin Genet
  
  Volume: 82(5) Issue: 5 Pages: 425-32
- DOI
  10.1111/j.1399-0004.2012.01897.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22791641, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-24390391, KAKENHI-PROJECT-24592573
[Journal Article] Thrombosis from a prothrombin mutation conveying antithrombin resistance.2012
- Author(s)
  Miyawaki Y, Suzuki A, Fujita J, Maki A, Okuyama E, Murata M, Takagi A, Murate T, Kunishima S, Sakai M, Okamoto K, Matsushita T, Naoe T, Saito H, Kojima T
- Journal Title
  
  N Engl J Med.
  
  Volume: 366 Issue: 25 Pages: 2390-2396
- DOI
  10.1056/nejmoa1201994
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22590524, KAKENHI-PROJECT-22591059, KAKENHI-PROJECT-22591755, KAKENHI-PROJECT-22659114, KAKENHI-PROJECT-23591429
[Journal Article] Identification of the integrin B3 L718P mutation in a pedigree with autosomal dominant thrombocytopenia with anisocytosis2012
- Author(s)
  Kobayashi Y
- Journal Title
  
  British Journal of Haematology
  
  Volume: 31 Issue: 4 Pages: 762-772
- DOI
  10.1111/bjh.12160
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-22591161, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-25293231
[Journal Article] G to T transversion at the first nucleotide of exon 26 of the MYH9 gene results in a novel missense mutation and abnormal splicing in platelets2012
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Med Genet
  
  Volume: 55 Issue: 12 Pages: 763-5
- DOI
  10.1016/j.ejmg.2012.09.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] A large family with MYH9 disorder caused by E1841K mutation suffering from serious kidney and hearing impairment and cataracts2012
- Author(s)
  Hao J, Kunishima S, Guo X, Hu R, Gao W
- Journal Title
  
  Ann Hematol
  
  Volume: 91(7) Issue: 7 Pages: 1147-8
- DOI
  10.1007/s00277-011-1370-5
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] Adams-Oliver syndrome and familial MYH9 mutation2012
- Author(s)
  Uyeda T, Echizenya T, Eto S, Ohtani K, Sato T, Takahashi T, Ito E, Yonesaka S, Kunishima S
- Journal Title
  
  Pediatr Int
  
  Volume: 54(3) Issue: 3 Pages: 407-9
- DOI
  10.1111/j.1442-200x.2011.03466.x
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] Early diagnosis improves the quality of life in MYH9 disorder2012
- Author(s)
  Shiota M, Kunishima S, Hamabata T, Nakata M, Hata D
- Journal Title
  
  Pediatr Blood Cancer
  
  Volume: 58(2) Issue: 2 Pages: 314-5
- DOI
  10.1002/pbc.23268
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] Unusual ribbon-like periventricular heterotopia with congenital cataracts in a Japanese girl2012
- Author(s)
  Tsuburaya R, Uematsu M, Kikuchi A, Hino-Fukuyo N, Kunishima S, Kato M, Haginoya K, Tsuchiya S
- Journal Title
  
  Am J Med Genet A
  
  Volume: 158A(3) Issue: 3 Pages: 674-7
- DOI
  10.1002/ajmg.a.34258
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-23659511
[Journal Article] Transient hemiparesis in a 14-year-old boy with MYH9 disorders2012
- Author(s)
  Kitamura K, Kunishima S, Tahara M, Ogiwara S, Dobata N, Dobata T, Sugihara A, Nakashima T, Sasaki Y, Nagumo K, Kubota M, Kinugawa Y, Ieko M, Kumaki S
- Journal Title
  
  Int J Hematol
  
  Volume: 96(3) Issue: 3 Pages: 376-9
- DOI
  10.1007/s12185-012-1149-z
- NAID
  10031121267
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] Heterozygous ITGA2B R995W mutation inducing constitutive activation of the {alpha}IIb{beta}3 receptor affects proplatelet formation and causes congenital macrothrombocytopenia2011
- Author(s)
  Kunishima S, Kashiwagi H, Otsu M, Takayama N, Eto K, Onodera M, Miyajima Y, Takamatsu Y, Suzumiya J, Matsubara K, Tomiyama Y, Saito H
- Journal Title
  
  Blood
  
  Volume: 117 Issue: 20 Pages: 5479-5484
- DOI
  10.1182/blood-2010-12-323691
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21300160, KAKENHI-PROJECT-21390321, KAKENHI-PROJECT-21591231, KAKENHI-PROJECT-21591242, KAKENHI-PLANNED-23106004, KAKENHI-PROJECT-23591429, KAKENHI-PROJECT-23659514, KAKENHI-PROJECT-23659533
[Journal Article] Efficacy of inchinkoto for a patient with liver fibrosis complicated with transient abnormal myelopoiesis in Down's syndrome2011
- Author(s)
  Takeyama M, Uchida Y, Arai I, Kamamoto T, Nishikubo T, Kanehiro H, Sado T, Kunishima S, Takahashi Y
- Journal Title
  
  Pediatr Int
  
  Volume: 53(6) Issue: 6 Pages: 1093-6
- DOI
  10.1111/j.1442-200x.2011.03365.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] Successful immunostaining demonstrates abnormal intracytoplasmic MYH9 protein (NMMHC-IIA) in neutrophils of a dog with May-Hegglin anomaly2011
- Author(s)
  Flatland B, Kunishima S
- Journal Title
  
  Vet Clin Pathol
  
  Volume: 40(4) Issue: 4 Pages: 409-10
- DOI
  10.1111/j.1939-165x.2011.00378.x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23591429
[Journal Article] A family of type 2B von Willebrand disease with R1306W mutation-severe thrombocytopenia leads to the normalization of high molecular weight multimers-.2010
- Author(s)
  Ozeki M, Kunishima S, Kasahara K, Funato M, Teramoto T, Kaneko H, Fukao T, Kondo N.
- Journal Title
  
  Thromb Res 125
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Advances in the understanding of MYH9 disorders.2010
- Author(s)
  Kunishima S
- Journal Title
  
  Curr Opin Hematol
  
  Volume: 17 Pages: 405-10
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] A novel splice site mutation in intron C of PROS1 leads to markedly reduced mutant mRNA level, absence of thrombin-sensitive region, and impaired secretion and cofactor activity of mutant protein2010
- Author(s)
  Okada H, Kunishima S, Hamaguchi M, Takagi A, Yamamoto K, Takamatsu J, Matsushita T, Saito H, Kojima T, Yamazaki T.
- Journal Title
  
  S.Thromb Res 125
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafness.2010
- Author(s)
  Kunishima S
- Journal Title
  
  Genet Test Mol Biomarkers 13
  
  Pages: 705-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] FLNA p.V528M substitution is neither associated with bilateral periven tricular nodular heterotopia nor with macrothrombocytopenia.2010
- Author(s)
  Kunishima S
- Journal Title
  
  J Hum Genet
  
  Volume: 55 Pages: 844-6
- NAID
  10030738152
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Paris-Trousseau-type macrothrombocytopenia without 11q deletion.2010
- Author(s)
  Kaya Z, Kocak U, Percin F, Kunishima S, Albayrak M, Gursel T, Ozogul C.
- Journal Title
  
  Pediatr Int. 52
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] FLNA p.V528M substitution is neither associated with bilateral periventricular nodular heterotopia nor with macrothrombocytopenia.2010
- Author(s)
  Kunishima S, Ito-Yamamura Y, Hayakawa A, Yamamoto T, Saito H.
- Journal Title
  
  J Hum Genet 55
  
  Pages: 844-6
- NAID
  10030738152
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Patients with Epstein?Fechtner syndromes owing to MYH9R702 mutations develop progressive proteinuric renal disease.2010
- Author(s)
  Sekine T, Konno M, Sasaki S, Moritani S, Miura T, Wong WS, Nishio H, Nishiguchi T, Yoshinari-Ohuchi M, Tsuchiya S, Matsuyama T, Kanegane H, Ida K, Miura K, Harita Y, Igarashi T, Hattori M, Horita S, Saito H, Kunishima S.
- Journal Title
  
  Kidney Int 78
  
  Pages: 207-14
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] MYH9により制御きれる血小板産生と血小板収縮機能.2009
- Author(s)
  國島伸治
- Journal Title
  
  血栓止血誌 20
  
  Pages: 301-6
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Mutation of the β1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly2009
- Author(s)
  Kunishima S
- Journal Title
  
  Blood 113
  
  Pages: 458-61
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] May-Hegglin 異常の分子病態2009
- Author(s)
  國島伸治
- Journal Title
  
  血液腫瘍科 58
  
  Pages: 103-8
- NAID
  40019065260
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Identification of three in-frame deletion mutations in MYH9 disorders suggesting an important hot spot for small rearrangements in MYH9 exon 24.2009
- Author(s)
  Miyazaki K, Kunishima S, Fujii W, Higashihara M.
- Journal Title
  
  Eur J Haematol 83
  
  Pages: 230-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Germinal mosaicism in MYH9 disorders : a family with two affected siblings of normal parents.2009
- Author(s)
  Kunishima S, Takaki K, Ito Y, Saito H.
- Journal Title
  
  Br J Haematol 145
  
  Pages: 260-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Germinal mosaicism in MYH9 disorders : a family with two affected siblings of normal parents.2009
- Author(s)
  Kunishima S
- Journal Title
  
  Br J Haematol 145
  
  Pages: 260-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Identification of the first in cis mutations in MYH9 disorder.2009
- Author(s)
  Miyajima Y, Kunishima S.
- Journal Title
  
  Eur J Haematol 82
  
  Pages: 288-91
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] 血小板減少症と血小板機能異常症2009
- Author(s)
  國島伸治
- Journal Title
  
  小児科内科増刊号小児疾患診療のための病態生理第4版 41
  
  Pages: 1117-23
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] 先天性巨大血小板症の診断.2009
- Author(s)
  國島伸治
- Journal Title
  
  日本内科学会誌 98
  
  Pages: 1593-8
- NAID
  10025192926
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] 先天性無巨核球性血小板減少症2009
- Author(s)
  國島伸治
- Journal Title
  
  分子細胞治療 8
  
  Pages: 129-133
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] 古くて新しい病気 May-Hegglin 異常-新しい検査と新しい概念-2009
- Author(s)
  國島伸治
- Journal Title
  
  臨床病理 57
  
  Pages: 54-9
- NAID
  10025224197
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Mutations in MYH9 exons 1, 16, 26, and 30 are infrequently found in Japanese patients with nonsyndromic deafness.2009
- Author(s)
  Kunishima S, Matsunaga T, Ito Y, Saito H.
- Journal Title
  
  Genet Test Mol Biomarkers 13
  
  Pages: 705-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Mutation of the β1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly.2009
- Author(s)
  Kunishima S, Kobayashi R, Itoh TJ, Hamaguchi M, Saito H.
- Journal Title
  
  Blood 113
  
  Pages: 458-61
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] 白血球封入体を伴う巨大血小板性血小板減少症とMYH9異常症2009
- Author(s)
  國島伸治
- Journal Title
  
  臨床病理 57
  
  Pages: 365-70
- NAID
  10025224748
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] A rare case of MYH9 disorders presenting with macrothrombocytopenia and deafness caused by MYH9-R702C mutation.2009
- Author(s)
  Kodama R, Taketani T, Kunishima S, Mishima S, Yoshikawa Y, Kanai R, Suyama T, Yoshino I, Kunishi H, Shibata H, Nagai A, Yamaguchi S, MasudaJ.
- Journal Title
  
  Thromb Res 124
  
  Pages: 508-11
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] A novel homozygous 8-base pair deletion mutation in the glycoprotein Ibα gene in a patient with Bernard-Soulier syndrome.2009
- Author(s)
  Imai C, Kunishima S, Takachi T, Iwabuchi H, Nemoto T, Imamura M, Uchiyama M.
- Journal Title
  
  Blood Coagul Fibrinolysis 20
  
  Pages: 470-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Identification and characterization of the first large MYH9 gene deletion associated with MYH9 disorders2008
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 80
  
  Pages: 540-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Characterization of a patient with atypical amegakaryocytic thrombocytopenia.2008
- Author(s)
  Kanaji S, Kanaji T, Migita M, Kunishima S, Kunicki TJ, Okamura T, Izuhara K.
- Journal Title
  
  Eur J Haematol 80
  
  Pages: 361-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Accumulation of MYH9 mRNA at leukocyte inclusion bodies in MYH9 disorders2008
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 81
  
  Pages: 325-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] 病気のはなしメイヘグリン異常2008
- Author(s)
  國島伸治
- Journal Title
  
  検査と技術 36
  
  Pages: 470-4
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders2008
- Author(s)
  Kunishima S
- Journal Title
  
  Blood 111
  
  Pages: 3015-23
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders.2008
- Author(s)
  Kunishima S, Hamaguchi M, Saito H.
- Journal Title
  
  Blood 111
  
  Pages: 3015-23
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Accumulation of MYH9 mRNA at leukocyte inclusion bodies in MYH9 disorders.2008
- Author(s)
  Kunishima S, Hirano K, Hamaguchi M, Saito H.
- Journal Title
  
  Eur J Haematol 81
  
  Pages: 325-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Identification and characterization of the first large MYH9 gene deletion associated with MYH9 disorders.2008
- Author(s)
  Kunishima S, Matsushita T, Hamaguchi M, Saito H.
- Journal Title
  
  Eur J Haematol 80
  
  Pages: 540-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] May-Hegglin 異常の新規鑑別診断法2008
- Author(s)
  國島伸治
- Journal Title
  
  日本検査血液学会誌 9
  
  Pages: 395-400
- Data Source
  KAKENHI-PROJECT-20591161
[Journal Article] Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations.2007
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 78
  
  Pages: 220-6
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] EBM of hemostatic examination. Diagnosis of platelet function disorders.2007
- Author(s)
  Kunishima S
- Journal Title
  
  Medical Technology 35
  
  Pages: 168-73
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] 特集止血系検査のEBM.血小板機能異常症の診断.2007
- Author(s)
  國島伸治
- Journal Title
  
  Medical Technology 35
  
  Pages: 168-73
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Haematological characteristics of MYH9 disorders due to MYH9R702 mutations.2007
- Author(s)
  Kunishima S
- Journal Title
  
  European Joumal of Haematology 78(3)
  
  Pages: 220-6
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations2007
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 78
  
  Pages: 220-6
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Haematological charactenstics of MYH9 disorders due to MYH9 R702 mutations.2007
- Author(s)
  Kunishima S
- Journal Title
  
  Eur H Haematol 78
  
  Pages: 220-6
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Novel heterozygous missense mutation in the second leucine rich repeat of GPIbα affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpura.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 76
  
  Pages: 348-55
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Gray platelet syndrome2006
- Author(s)
  Kunishima S
- Journal Title
  
  Ketsueki Frontier 16
  
  Pages: 106-12
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Novel heterozygous missense mutation in the second leucine rich repeat of GPIbα affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpura2006
- Author(s)
  Kunishima S
- Journal Title
  
  European Jounrnal of Haematology 76(4)
  
  Pages: 348-355
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] 先天性巨大血小板症の遺伝子診断.2006
- Author(s)
  國島伸治
- Journal Title
  
  日小血会誌 20
  
  Pages: 95-7
- NAID
  10017439442
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan is frequently misdiagnosed as idiopathic thrombocytopenic purpura.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Int J Hematol 83
  
  Pages: 366-7
- NAID
  10017475827
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Congenital macrothrombocytopenias2006
- Author(s)
  Kunishima S
- Journal Title
  
  Blood Reviews 20(2)
  
  Pages: 111-21
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Gray platelet症候群.2006
- Author(s)
  國島伸治
- Journal Title
  
  血液フロンティア 16
  
  Pages: 106-12
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Further characterization of anti-platelet monoclonal antibody HPL5 as anti-glycoprotein V antibody2006
- Author(s)
  Kunishima S
- Journal Title
  
  Acta Haematologica 115(1,2)
  
  Pages: 128-30
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan is frequently misdiagnosed as idiopathic thrombocytopenic purpura.2006
- Author(s)
  Kunishima S
- Journal Title
  
  International Journal of Hematology 83(4)
  
  Pages: 366-7
- NAID
  10017475827
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Congenital macrothrombocytopenias.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Blood Rev 20
  
  Pages: 111-21
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Molecular genetic analysis of a valiant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Eur H Haematol 77
  
  Pages: 501-12
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Further characterization of anti-platelet monoclonal antibody HPL5 as anti-glycoprotein V antibody.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Acta Haematol 115
  
  Pages: 128-30
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Molecular genetic analysis of a variant Bemard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations.2006
- Author(s)
  Kunishima S
- Journal Title
  
  European Journal of Haematology 76(6)
  
  Pages: 501-12
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Further characterization of anti-platelet monoclonal antibody HPL5 as anti-glycoprotein V antibody2006
- Author(s)
  Kunishima S
- Journal Title
  
  Acta Haematologica 115(1,2)
  
  Pages: 128-30
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] Novel heterozygous missense mutation in the second leucine rich repeat of GPIbα affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpura.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Eur H Haematol 76
  
  Pages: 348-55
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Novel heterozygous missense mutation in the second leucine rich repeat of GPIbα affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpura2006
- Author(s)
  Kunishima S
- Journal Title
  
  European Journal of Haematology 76(4)
  
  Pages: 348-55
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibβ mutations.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 77
  
  Pages: 501-12
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Congenital macrothrombocytopenias2006
- Author(s)
  Kunishima S
- Journal Title
  
  Blood Reviews 20(2)
  
  Pages: 111-21
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] Novel heterozygous missense mutation in the second leucine rich repeat of GPIbα affects GPIb/IX/V expression and results in macrothrombocytopenia in a patient initially misdiagnosed with idiopathic thrombocytopenic purpura2006
- Author(s)
  Kunishima S
- Journal Title
  
  European Journal of Haematology 76(4)
  
  Pages: 348-55
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] Genetic diagnosis of congenital macrothrothrombocytopenias.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Jap J Pedoatr Hematol 20
  
  Pages: 95-7
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan is frequently misdiagnosed as idiopathic thrombocytopenic purpura.2006
- Author(s)
  Kunishima S
- Journal Title
  
  Int J Haematol 83
  
  Pages: 366-7
- NAID
  10017475827
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] First description of somatic mosaicism in MYH9 disorders2005
- Author(s)
  Kunishima S
- Journal Title
  
  Br J Haematol 128・3
  
  Pages: 360-365
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Detection of unique neutrophil nonmuscle myosin heavy chain-A localization by immunofluorescence analysis in MYH9 disorder presented with macrothrombocytopenia without leukocyte inclusions and deafness2005
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 74・1
  
  Pages: 1-5
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] First description of somatic mosaicism in MYH9 disorders2005
- Author(s)
  Kunishima S
- Journal Title
  
  Br J Haematol 128・3
  
  Pages: 360-365
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] Detection of unique neutrophil nonmuscle myosin heavy chain-A localization by immunofluorescence analysis in MYH9 disorder presented with macrothrombocytopenia without leukocyte inclusions and deafness2005
- Author(s)
  Kunishima S
- Journal Title
  
  Eur J Haematol 74・1
  
  Pages: 1-5
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders.
- Author(s)
  Kunishima S
- Journal Title
  
  Blood (印刷中)
- Description
  「研究成果報告書概要(和文)」より
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan : frequently misdiagnosed as idiopathic thrombocytopenic purpura
- Author(s)
  Kunishima S
- Journal Title
  
  International Journal of Hematology In press
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan : Frequently misdiagnosed as idiopathic thrombocytopenic purpura
- Author(s)
  Kunishima S
- Journal Title
  
  International Journal of Hematology (in press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan : frequently misdiagnosed as idiopathic thrombocytopenic purpura
- Author(s)
  Kunishima S
- Journal Title
  
  International Journal of Hematology (In press)
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-16590971
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan : frequently misdiagnosed as idiopathic thrombocytopenic purpura
- Author(s)
  Kunishima S
- Journal Title
  
  International Journal of Hematology In press
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders.
- Author(s)
  Kunishima S
- Journal Title
  
  Blood (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Differential expression of wild-type and mutant NMMHC-IIA polypeptides in blood cells suggests cell-specific regulation mechanisms in MYH9 disorders.
- Author(s)
  Kunishima S
- Journal Title
  
  Blood (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan : frequently misdiagnosed as idiopathic thrombocytopenic purpura
- Author(s)
  Kunishima S
- Journal Title
  
  International Journal of Hematology (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16390283
[Journal Article] Genetic abnormalities of inherited thrombocytopemas.
- Author(s)
  Kunishima S
- Journal Title
  
  Annual Review 2006 hematology
  
  Pages: 205-212
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Journal Article] Bernard-Soulier syndrome due to GPIX W127X mutation in Japan : frequently misdiagnosed as idiopathic thrombocytopenic purpura
- Author(s)
  Kunishima S
- Journal Title
  
  International Journal of Hematology (in press)
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-16590971
[Presentation] 先天性血小板減少症・異常症の新しい診断体制とレジストリの確立2021
- Author(s)
  石黒精、内山徹、要匡、武部淳子、秦健一郎、小原收、笹原洋二、國島伸治
- Organizer
  第43回日本血栓止血学会学術集会
- Data Source
  KAKENHI-PROJECT-18K07809
[Presentation] MYH9 Disorders in Thailand: Pediatric Case Series from Thai Macrothrombocytopenia Study Group2019
- Author(s)
  Natesirinilkul R, Sosothikul D, Komiwilaisak P, Pongtanakul B, Mekjarusgul P, Kunishima S, Sirachainan N
- Organizer
  XXVII Congress of the International Society on Thrombosis and Haemostasis
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07809
[Presentation] Molecular genetic analysis of 10 families with chronic thrombocytopenia2019
- Author(s)
  Yuri Uchiyama1,2, Yoshiyuki Ogawa3, Kunio Yanagisawa3, Shinji Kunishima4, Takeshi Mizuguchi1, Hideki Uchiumi3, Hiroshi Handa3 and Naomichi Matsumoto
- Organizer
  XXVII Congress of the International Society on Thrombosis and Haemostasis
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07809
[Presentation] Differential diagnosis of congenital macrothrombocytopenia -12-year experience in Nagoya-2016
- Author(s)
  Kunishima S, Saito H
- Organizer
  Platelets2016: 9th International Symposium
- Place of Presentation
  Wellesley, Massachusette, USA
- Year and Date
  2016-09-16
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] 新規検査法により診断された先天性巨大血小板症2016
- Author(s)
  國島伸治　北村勝誠　山村喜美
- Organizer
  第70回国立病院総合医学会
- Place of Presentation
  那覇
- Year and Date
  2016-11-11
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] Further classification of neutrophil non-muscle myosin heavy chain IIA localization for efficient genetic diagnosis of MYH9 disorders2016
- Author(s)
  Kunishima S, Kada A, Hao J
- Organizer
  XXIX International Symposium on Technical Innovations in Laboratory Hematology
- Place of Presentation
  Milano, Italy
- Year and Date
  2016-05-12
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] MYH9異常症遺伝子診断のための好中球ミオシン局在解析の細分類2016
- Author(s)
  國島伸治　嘉田晃子　Hao Jihong　北村勝誠
- Organizer
  第38回日本血栓止血学会学術集会
- Place of Presentation
  奈良
- Year and Date
  2016-06-16
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] 原因不明の血小板減少症と診断されていた2B型von Willebrand病の親子例2015
- Author(s)
  國島伸治　北村勝誠　八田京子
- Organizer
  第16回日本検査血液学会学術集会
- Place of Presentation
  名古屋
- Year and Date
  2015-07-11
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] Functional Characterization of a Novel GFI1B Mutation Causing Congenital Macrothrombocytopenia2015
- Author(s)
  Katsumasa Kitamura, Yusuke Okuno, Kenichi Yoshida, Masashi Sanada, Yuichi Shiraishi, Hideki Muramatsu, Ryoji Kobayashi, Satoru Miyano, Seiji Kojima, Seishi Ogawa, Shinji Kunishima
- Organizer
  57th American Society for Hematology Annual Meeting and Exposition, 5-8 December 2015, Orlando, FL, USA.
- Place of Presentation
  米国、オーランド
- Year and Date
  2015-12-05
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] Genetic basis of congenital macrothrombocytopenia2015
- Author(s)
  Shinji Kunishima
- Organizer
  International Society on Thrombosis and Haemostasis Academy
- Place of Presentation
  Webinar
- Year and Date
  2015-03-25
- Invited
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] 診断の迷宮-判断に迷う疾患へのアプローチ-2015
- Author(s)
  國島伸治
- Organizer
  第16回日本検査血液学会学術集会
- Place of Presentation
  名古屋
- Year and Date
  2015-07-11
- Invited
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] 幹細胞技術の検査医学研究への応用2014
- Author(s)
  國島伸治
- Organizer
  第33回日本臨床検査医学会東海北陸支部例会
- Place of Presentation
  名古屋
- Year and Date
  2014-08-02
- Invited
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] 先天性血小板減少症の分子病態と鑑別診断2014
- Author(s)
  國島伸治
- Organizer
  第32回青森小児血液・腫瘍研究会
- Place of Presentation
  青森
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 発熱時の採血を契機としてMay-Hegglin異常の診断に至った男児例2014
- Author(s)
  西村美穂　八戸由佳子　中川慎一郎　松尾陽子　大園秀一　上田耕一郎　稲田浩子　松石豊次郎　村上義比古　國島伸治
- Organizer
  第478回日本小児科学会福岡地方会例会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板症(シンポジウム「次世代シーケンサーによる小児血液、腫瘍疾患における研究の進展)2013
- Author(s)
  國島伸治
- Organizer
  第55回日本小児血液・がん学会学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Inherited platelet disorders2013
- Author(s)
  Shinji Kunishima
- Organizer
  International Workshop on Hemostasis and Thrombosis,
- Place of Presentation
  Bangkok
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 腎障害の経過が緩徐なEpstein症候群の1例2013
- Author(s)
  遣田美貴　菅野直希　古谷麻衣子　坪井伸夫　宮崎陽一　小倉誠　徳留悟朗　細谷龍男　横尾隆　海渡健　國島伸治
- Organizer
  第43回日本腎臓学会東部学術大会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性血小板異常症の分子病-先天性巨大血小板症-2013
- Author(s)
  國島伸治
- Organizer
  第35回日本血栓止血学会学術集会
- Place of Presentation
  山形, (教育講演)
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] MYH9異常症における免疫蛍光染色の有用性2013
- Author(s)
  北村勝誠　國島伸治　吉田健一　小川誠司　白石友一　千葉健一　田中洋子　宮野悟　古川鋼一
- Organizer
  第55回日本小児血液・がん学会学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性血小板減少症の分子病態と鑑別診断2013
- Author(s)
  國島伸治
- Organizer
  第17回栃木県血液疾患講演会
- Place of Presentation
  宇都宮
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Demonstration of novel gain-of-function mutations of aIIbβ3: association with macrothrombocytopenia and Glanzmann thrombasthenia-like phenotype2013
- Author(s)
  Hirokazu Kashiwagi, Shinji Kunishima, Kazunobu Kiyomizu, Yoshiro Amano, Hiroyuki Shimada, Masashi Morishita, Yuzuru Kanakura, Yoshiaki Tomiyama
- Organizer
  XXIV Congress of the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Amsterdam
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性血小板異常症の分子病態2013
- Author(s)
  國島伸治
- Organizer
  第35回日本血栓止血学会学術集会
- Place of Presentation
  山形
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板症2013
- Author(s)
  國島伸治
- Organizer
  第55回日本小児血液・がん学会学術集会
- Place of Presentation
  福岡
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性血液疾患の病態研究に関する最近の進歩2013
- Author(s)
  國島伸治
- Organizer
  第116回日本小児科学会学術集会
- Place of Presentation
  広島
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 難聴を伴ったMay-Hegglin異常の家族例2013
- Author(s)
  金田　眞　鳥海尚久　更科岳大　國島伸治　東　寛
- Organizer
  第116回日本小児科学会学術集会
- Place of Presentation
  広島
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Platelet function tests2013
- Author(s)
  Shinji Kunishima
- Organizer
  International Workshop on Hemostasis and Thrombosis,
- Place of Presentation
  Bangkok, Thailand
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Impaired proplatelet formation in a novel Glanzmann variant macrothrombocytopenia2013
- Author(s)
  Koji Miyazaki, Shinji Kunishima, Hirokazu Kashiwagi, Yoshiaki Tomiyama, Masaaki, Higashihara
- Organizer
  18th Congress of the European Hematology Association
- Place of Presentation
  Stockholm
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Successful treatment of MYH9 disorders with romiplostim for neurosurgery2013
- Author(s)
  Jun Yamanouchi, Takaaki Hato, Toshiyuki Niiya, Shinji Kunishima, Masaki Yasukawa
- Organizer
  第75回日本血液学会総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] ACTN1 mutations cause congenital macrothrombocytopenia (symposium) XXIV Congress of2013
- Author(s)
  Shinji Kunishima, Yusuke Okuno, Masashi Sanada, Koji Miyazaki, Michio Sakai, Akihiro Iguchi, Satoru Miyano, Hidehiko Saito, Seiji Kojima, and Seishi Ogawa
- Organizer
  the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Amsterdam
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Aberrant mRNA processing in compound heterozygote with glycoprotein IIb gene mutations causing Glanzmann thrombasthenia2013
- Author(s)
  Junko Fujita, Moe Murata, Yoko Kajiura, Akira Takagi, Takashi Murate, Tadashi Matsushita, Shinji Kunishima, Tetsuhito Kojima
- Organizer
  XXIV Congress of the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Amsterdam
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性血液疾患の病態研究に関する最近の進歩2013
- Author(s)
  國島伸治
- Organizer
  第116回日本小児科学会学術集会, (シンポジウム)血小板異常症
- Place of Presentation
  広島
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] A case of MYH9 disorder with kidney dysfunction successfully treated by Eltrombopag for inherited thrombocytopenia2013
- Author(s)
  Eri Tanaka, Naoko Kinugawa, Shinji Kunishima
- Organizer
  18th Congress of the European Hematology Association
- Place of Presentation
  Stockholm
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板症の病因解明と鑑別診断の進歩2013
- Author(s)
  國島伸治
- Organizer
  第23回日本産婦人科・新生児血液学会学術集会
- Place of Presentation
  奈良
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 血小板減少と末梢血標本の観察からtype2B VWDの診断に至った１症例2013
- Author(s)
  前田奈弥　高津真由美　亀山なつみ　杉浦由姫乃　三田直美　稲垣恵章　松本祐之　濱麻人　國島伸治　松下正
- Organizer
  第14回日本検査血液学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Mutations responsible for ANKRD26-related thrombocytopenia increase the risk of hematological malignancies but are not frequently involved in de novo acute leukemias2013
- Author(s)
  Carlo Balduini, Gennifer Yu, Paula Heller, Marie-Christine Alessi, Paola Giordano, Shinji Kunishima, et al.
- Organizer
  18th Congress of the European Hematology Association
- Place of Presentation
  Stockholm
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Dominant inheritance of familial thrombocytopenia caused by integrin αIIbβ3 (GPIIb/IIIa) mutation2013
- Author(s)
  Tsumura M, Kobayashi Y, Matsui H, Kanai A, Okada S, Miki M, Nakamura K, Kunishima S, Inaba T, Kobayashi M
- Organizer
  第75回日本血液学会総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 周産期血液疾患のUp to Date「先天性巨大血小板症の病因解明と鑑別診断の進歩」(ワークショップ)2013
- Author(s)
  國島伸治
- Organizer
  第23回日本産婦人科・新生児血液学会学術集会
- Place of Presentation
  奈良
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] ACTN1 mutations cause congenital macrothrombocytopenia2013
- Author(s)
  Shinji Kunishima, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Masashi Sanada, Hideki Muramatsu, Kenichi Chiba, Hiroko Tanaka, Koji Miyazaki, Michio Sakai, Masatoshi Ohtake, Ryoji Kobayashi, Akihiro Iguchi, Gen Niimi, Makoto Otsu, Yoshiyuki Takahashi, Satoru Miyano, Hidehiko Saito, Seiji Kojima, and Seishi Ogawa
- Organizer
  第75回日本血液学会総会
- Place of Presentation
  札幌
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 針生検施行時に出血傾向の存在が疑われた巨大血小板性血小板減少症(GPD)の1例2013
- Author(s)
  小川孔幸　柳澤邦雄　林　俊誠　合田　史　馬渡桃子　内海英貴　鬼頭有里　國島伸治
- Organizer
  第35回日本血栓止血学会学術集会
- Place of Presentation
  山形
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] ACTN1 mutations cause congenital macrothrombocytopenia2013
- Author(s)
  Shinji Kunishima, Yusuke Okuno, Masashi Sanada, Koji Miyazaki, Michio Sakai, Akihiro Iguchi, Satoru Miyano, Hidehiko Saito, Seiji Kojima, and Seishi Ogawa
- Organizer
  XXIV Congress of the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Amsterdam
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 血小板減少を契機にvon Willebrand病type2Bと診断された2家系の遺伝子解析2013
- Author(s)
  三田直美　田中竜平　岸本麿由子　鈴木伸明　國島伸治　高津真由美　松本祐之　中村栄男　松下正
- Organizer
  第35回日本血栓止血学会学術集会
- Place of Presentation
  山形
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Genetic analyses of two patients with von Willebrand disease (VWD) type2B Implication of type 2B in the differential diagnosis for thrombocytopenic patients2013
- Author(s)
  Naomi Sanda, Ryuhei Tanaka, Mayuko Kishimoto, Nobuaki Suzuki, Shinji Kunishima, Mayumi Takatsu, Hiroyuki Matsumoto, Shigeo Nakamura, Tadashi Matsushita
- Organizer
  XXIV Congress of the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Amsterdam
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Inherited platelet disorders2013
- Author(s)
  Shinji Kunishima
- Organizer
  International Workshop on Hemostasis and Thrombosis, (Symposium)
- Place of Presentation
  Bangkok, Thailand
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Platelet function tests2013
- Author(s)
  Shinji Kunishima
- Organizer
  International Workshop on Hemostasis and Thrombosis, (Symposium)
- Place of Presentation
  Bangkok, Thailand
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板症(教育セッション7血小板・ITP)2012
- Author(s)
  國島伸治
- Organizer
  第53回日本小児血液・がん学会学術集会
- Place of Presentation
  前橋, (教育講演)
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 母子間HPA-21bw不適合に認められた一過性巨大血小板症2012
- Author(s)
  國島伸治, 早川晶, 藤田花織
- Organizer
  第20回小児ITP研究会
- Place of Presentation
  東京
- Year and Date
  2012-11-17
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板症2011
- Author(s)
  國島伸治
- Organizer
  第53回日本小児血液・がん学会学術集会(招待講演)
- Place of Presentation
  前橋
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Diagnosis of congenital macrothrombocytopenias2011
- Author(s)
  Shinji Kunishima
- Organizer
  XXIII Congress of the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Kyoto
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Diagnosis of congenital macrothrombocytopenias2011
- Author(s)
  Shinji Kunishima
- Organizer
  XXIII Congress of the International Society on Thrombosis and Haemostasis(招待講演)
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性血小板減少症の鑑別診断2011
- Author(s)
  國島伸治
- Organizer
  第19回日本小児ITP研究会(招待講演)
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板性血小板減少症2011
- Author(s)
  國島伸治
- Organizer
  先天性造血不全シンポジウム
- Place of Presentation
  浦安市
- Year and Date
  2011-02-05
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Identical twins of Epstein/Fechtner syndrome with MYH9 R702C mutaions2011
- Author(s)
  Ohwada Y, Suzumura H, Sugita K, Kanou K, Arisaka O, Tomita S, Ueda U, Sekine T, Kunishima S
- Organizer
  The 11th Asian Congress of Pediatric Nephrology
- Place of Presentation
  Fukuoka, Japan
- Year and Date
  2011-06-04
- Data Source
  KAKENHI-PROJECT-23591586
[Presentation] May-Hegglin異常単球における封入体2011
- Author(s)
  國島伸治
- Organizer
  第12回日本検査血液学会学術集会
- Place of Presentation
  倉敷
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板性血小板減少症2011
- Author(s)
  國島伸治
- Organizer
  先天性造血不全シンポジウム
- Place of Presentation
  浦安
- Year and Date
  2011-02-05
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 異常単球における封入体2011
- Author(s)
  國島伸治, Hao Jihong(郝冀洪), 山村喜美, May-Hegglin
- Organizer
  第12回日本検査血液学会学術集会
- Place of Presentation
  倉敷
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] 先天性巨大血小板症の病因・病態解析と鑑別診断2010
- Author(s)
  國島伸治
- Organizer
  第8回血液・血管オルビス
- Place of Presentation
  東京都(指名講演)
- Year and Date
  2010-08-22
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板性血小板減少症家系において見いだした新規GPIIIa遺伝子変異2010
- Author(s)
  國島伸治
- Organizer
  第52回日本小児血液学会総会
- Place of Presentation
  大阪市
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] GPIIb/IIIa異常による新規先天性巨大血小板症2010
- Author(s)
  國島伸治
- Organizer
  第18回日本小児ITP研究会
- Place of Presentation
  東京都
- Year and Date
  2010-11-20
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板性血小板減少症家系において見いだした新規GPIIIa遺伝子変異2010
- Author(s)
  國島伸治
- Organizer
  第52回日本小児血液学会総会
- Place of Presentation
  大阪
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症における新規GPIIb変異の同定2010
- Author(s)
  國島伸治
- Organizer
  第11回日本検査血液学会学術集会
- Place of Presentation
  東京都
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] NHOネットワーク共同研究-先天性血小板減少症の診断ガイドライン作成に関する研究-2010
- Author(s)
  國島伸治
- Organizer
  第64回国立病院総合医学会
- Place of Presentation
  福
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Molecular mechanisms for macrothrombocytopenia2010
- Author(s)
  國島伸治
- Organizer
  第72回日本血液学会総会
- Place of Presentation
  横浜市
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症の病因・病態解析と鑑別診断2010
- Author(s)
  國島伸治
- Organizer
  第8回血液・血管オルビス
- Place of Presentation
  東京
- Year and Date
  2010-08-22
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] GPIIb/IIIa異常による新規先天性巨大血小板症2010
- Author(s)
  國島伸治
- Organizer
  第18回日本小児ITP研究会
- Place of Presentation
  東京
- Year and Date
  2010-11-20
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症における新規GPIIb変異の同定2010
- Author(s)
  國島伸治
- Organizer
  第11回日本検査血液学会学術集会
- Place of Presentation
  東京
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Molecular mechanisms for macrothrombocytopenia2010
- Author(s)
  國島伸治
- Organizer
  第72回日本血液学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] NHOネットワーク共同研究-先天性血小板減少症の診断ガイドライン作成に関する研究-2010
- Author(s)
  國島伸治
- Organizer
  第64回国立病院総合医学会
- Place of Presentation
  福岡市
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症の鑑別診断-九州沖縄地域の特徴を含めて-(教育講演)2009
- Author(s)
  國島伸治
- Organizer
  日本検査血液学会沖縄支部第7回学術集会
- Place of Presentation
  那覇
- Year and Date
  2009-12-05
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] A heterozygous ITGA2B R995W mutation causes constitutive activation of the αIIbβ3 receptor and results in congenital macrothrombocytopenia2009
- Author(s)
  Shinji Kunishima
- Organizer
  XXII Congress of the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Boston, MA,USA
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] GPIbβ点変異と22q11.2欠失との複合ヘテロ型異常によるBernard-Soulier症候群2009
- Author(s)
  國島伸治
- Organizer
  第51回日本小児血液学会総会
- Place of Presentation
  千葉
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] von Willebrand病type 2Bと巨大血小板症2009
- Author(s)
  國島伸治
- Organizer
  日本血栓止血学会学術標準化委員会第4回SSCシンポジウム
- Place of Presentation
  東京
- Year and Date
  2009-11-21
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] メイ・ヘグリン異常の原因遺伝子の同定、鑑別診断法の確立と新規疾患概念の提唱2009
- Author(s)
  國島伸治
- Organizer
  愛知県臨床衛生検査技師会遺伝子染色体検査研究班例会
- Place of Presentation
  名古屋
- Year and Date
  2009-11-14
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 小児の先天性血小板減少症(特別講演)2009
- Author(s)
  國島伸治
- Organizer
  第23回滋賀小児感染症・血液疾患研究会
- Place of Presentation
  大津
- Year and Date
  2009-10-31
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性血小板減少症の鑑別診断(特別講演)2009
- Author(s)
  國島伸治
- Organizer
  第26回北海道小児血液研究会
- Place of Presentation
  札幌
- Year and Date
  2009-10-17
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症の新たな原因GPIIb R995W変異2009
- Author(s)
  國島伸治
- Organizer
  第10回日本検査血液学会学術集会
- Place of Presentation
  甲府
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性血小板減少症の鑑別診断2009
- Author(s)
  國島伸治
- Organizer
  第26回北海道小児血液研究会
- Place of Presentation
  札幌
- Year and Date
  2009-10-17
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Congenital amegakaryocytic thrombocytopenia.2009
- Author(s)
  國島伸治
- Organizer
  16^<th> Annual Meeting of the Japan Childhood Aplastic Anemia Study Group.
- Place of Presentation
  Nagoya
- Year and Date
  2009-05-30
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Congenital amegakaryotcytic thrombocytopenia2009
- Author(s)
  Shinji Kunishima
- Organizer
  16^<th> Annual Meeting of the Japan Childhood Aplastic Anemia Study Group
- Place of Presentation
  名古屋
- Year and Date
  2009-05-30
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 小児の先天性血小板減少症2009
- Author(s)
  國島伸治
- Organizer
  第23回滋賀小児感染症・血液疾患研究会
- Place of Presentation
  大津
- Year and Date
  2009-10-31
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症の鑑別診断-九州沖縄地域の特徴を含めて-2009
- Author(s)
  國島伸治
- Organizer
  日本検査血液学会沖縄支部第7回学術集会
- Place of Presentation
  那覇
- Year and Date
  2009-12-05
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] A heterozygous ITGA2BR995W mutation causes constitutive activation of theαIIbβ3receptor and results in congenital macrothrombocytopenia2009
- Author(s)
  國島伸治
- Organizer
  XXII Congress of the International Society on Thrombosis and Haemostasis.
- Place of Presentation
  Boston, MA, USA
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] May-Hegglin 異常の新規鑑別診断法(シンポジウム血小板関連疾患の病態と診断の進歩)2008
- Author(s)
  國島伸治
- Organizer
  第9回日本検査血液学会学術集会
- Place of Presentation
  津
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Differential diagnosis of macrothrombocytopenias.2008
- Author(s)
  國島伸治
- Organizer
  The XXXIInd World Congress of the International Society of Hematology.
- Place of Presentation
  Bangkok, Thailand
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Congenital Macrothiombocytopenias, clinics, diagnosis, and pathology.2008
- Author(s)
  Kunishima S
- Organizer
  14th Kansai Thrombisis Forum
- Place of Presentation
  Osaka
- Year and Date
  2008-01-19
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] 先天性巨大血小板症の鑑別診断(特別講演)2008
- Author(s)
  國島伸治
- Organizer
  第46回東海小児血液懇話会
- Place of Presentation
  名古屋
- Year and Date
  2008-02-12
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] 血小板異常症についての話題2008
- Author(s)
  國島伸治
- Organizer
  第9回東海KOAG研究会
- Place of Presentation
  名古屋
- Year and Date
  2008-09-11
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Differential diagnosis of macrothrombocytopenias.2008
- Author(s)
  國島伸治
- Organizer
  The XXXIInd World Congress of the International Societyof Hematology
- Place of Presentation
  Bangkok, Thailand
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症の臨床、診断、病態(特別講演)2008
- Author(s)
  國島伸治
- Organizer
  第14回関西血栓フォーラム
- Place of Presentation
  大阪
- Year and Date
  2008-01-19
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Differential diagnosis of macrothrombocytopenias (Symposium)2008
- Author(s)
  Shinji Kunishima
- Organizer
  The XXXIInd World Congress of the International Society of Hematology
- Place of Presentation
  Bangkok, Thailand
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] MYH9遺伝子exon1に2種類の新規遺伝子変異を同時に認めたMay-Hegglin異常の1例2008
- Author(s)
  國島伸治
- Organizer
  第70回日本血液学会総会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 先天性巨大血小板症の鑑別診断(特別講演)2008
- Author(s)
  國島伸治
- Organizer
  第43回東海小児血液懇話会
- Place of Presentation
  名古屋
- Year and Date
  2008-02-12
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] 血小板異常症についての話題 (特別講演)2008
- Author(s)
  國島伸治
- Organizer
  第9回東海KOAG研究会
- Place of Presentation
  名古屋
- Year and Date
  2008-09-11
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 古くて新しい病気 May-Hegglin 異常-新しい検査と新しい概念-(シンポジウム)2008
- Author(s)
  國島伸治
- Organizer
  第27回日本臨床検査医学会東海北陸支部例会
- Place of Presentation
  浜松
- Year and Date
  2008-08-31
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Differential diagnosis of congenital macrothrombocytopenias.2008
- Author(s)
  Kunishima S
- Organizer
  43th Tokai Gathering for Pediatric Hematology
- Place of Presentation
  Nagoya
- Year and Date
  2008-02-12
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] 古くて新しい病気May-Hegglin異常-新しい検査と新しい概念-2008
- Author(s)
  國島伸治
- Organizer
  第27回日本臨床検査医学会東海北陸支部例会
- Place of Presentation
  浜松
- Year and Date
  2008-08-31
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] 新たな先天性巨大血小板症の原因となるインテグリンαIIb変異2008
- Author(s)
  國島伸治
- Organizer
  第70回日本血液学会総会
- Place of Presentation
  京都
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] May-Hegglin異常の新規鑑別診断法2008
- Author(s)
  國島伸治
- Organizer
  第9回日本検査血液学会学術集会
- Place of Presentation
  津
- Data Source
  KAKENHI-PROJECT-20591161
[Presentation] Differential detection of wild-type and mutant MYH9 mRNA and NMMHC-IIA polypeptide reveals dominant negative effect in granulocytes and haploinsufficiency in platelets in patients with MYH9 disorders2007
- Author(s)
  Kunishima S
- Organizer
  XXIst Congress of the International Society on Thrombosis and Haemostasis,
- Place of Presentation
  Geneva, Switzerland
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Utility of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-IIa in the differential diagnosis of macrothrombocytopenias.2007
- Author(s)
  Kunishima S
- Organizer
  11th Congress of the International Society of Hematology, Asian-Pacific Division
- Place of Presentation
  Beijing, China
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] 先天性巨大血小板症の診断の進歩(ワークショップ)2007
- Author(s)
  國島伸治
- Organizer
  第8回日本検査血液学会学術集会
- Place of Presentation
  福井
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Congenital macrothrombocytopenia due to a β1-tubulin mutation.2007
- Author(s)
  Kunishima S
- Organizer
  69th Annual meeting of Japanese Society of Hematology. 49th annual meeting of Japanese Society of Clinical Hematology
- Place of Presentation
  Yokohama
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Utility of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-IIa in the differential diagnosis of macrothrombocytopenias.2007
- Author(s)
  Kunishima S
- Organizer
  11th Congress of the International Society of Hematology, Asian-Pacific Division
- Place of Presentation
  Beijing,China
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] b1-tubulin異常による先天性巨大血小板症2007
- Author(s)
  國島伸治
- Organizer
  第69回日本血液学会総会・第49回日本臨床血液学会総会
- Place of Presentation
  横浜
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Utility of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-IIa in the differential diagnosis of macrothrombocytopenias.2007
- Author(s)
  Kunishima S
- Organizer
  11th Congress of the International Society of Hemotology, Asian-Pacific Division
- Place of Presentation
  Beijing, China
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Differential detection of wild-type and mutant MYH9 mRNA and NMMHC-IIA polypeptide reveals dominant negative effect in granulocytes and happloinsufficiency in platelets in patients with MYH9 disorders2007
- Author(s)
  Kunishima S
- Organizer
  XXIst Congress of the International Society on Thrombosis and Haemostasis,
- Place of Presentation
  Geneva,Switzerland
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] MYH9異常症における異常ミオシンの細胞別発現2007
- Author(s)
  國島伸治
- Organizer
  第30回日本血栓止血学会学術集会
- Place of Presentation
  志摩
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Differential detection of wild-type and mutant MYH9mRNA and NMMHC-IIA polypeptide reveals dominant negative effect in granulocytes and happloinsufficiency in platelets in patients with MYH9 disorders.2007
- Author(s)
  Kunishima S
- Organizer
  XXIst Congress of the International Society on Thrombosis and Haemostasis
- Place of Presentation
  Switzerland
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Progress of genetic diagnosis of congenital macrothrombocytopenias.2007
- Author(s)
  Kunishima S
- Organizer
  8th Congress of Japanese Society for Laboratory Hematology
- Place of Presentation
  Fukui
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] β1-tubulin異常による先天性巨大血小板症2007
- Author(s)
  國島伸治
- Organizer
  第69回日本血液学会総会・第49回日本臨床血液学会総会
- Place of Presentation
  横浜
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] MYH9遺伝子R702変異によるMYH9異常症の特徴2006
- Author(s)
  國島伸治
- Organizer
  第68回日本血液学会総会・第48回日本臨床血液学会総会
- Place of Presentation
  福岡
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] 遺伝性血小板減少症の遺伝子異常2006
- Author(s)
  國島伸治
- Organizer
  Annual Review 2006 血液(高久史麿, 溝口秀昭, 坂田洋一, 金倉譲、小島勢二編集)
- Place of Presentation
  205-212
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Charactristics of MYH9 disorders due to MYH9 R702 mutations.2006
- Author(s)
  Kunishima S
- Organizer
  59th Tokai Thrombosis Seminor
- Place of Presentation
  Nagoya
- Year and Date
  2006-10-21
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Charactristics of MYH9 disorders due to MYH9 R702 mutations.2006
- Author(s)
  Kunishima S
- Organizer
  68th Annual meeting of Japanese Society of Hematology. 48th annual meeting of Japanese Society of Clinical Hematology
- Place of Presentation
  Fukuoka
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Utility of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-IIA in the differential diagnosis of congenital macrothrombocytopenias.2006
- Author(s)
  Kunishima S
- Organizer
  XIXth International Symposium on Technological Innovations in Laboratory Hematology, ISLH2006 Amsterdam
- Place of Presentation
  Amsterdam, the netherlands
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Bernard-Soulier症候群および保因者の血小板サイズに関する研究2006
- Author(s)
  國島伸治
- Organizer
  第7回日本検査血液学会学術集会
- Place of Presentation
  東京
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] MYH9遺伝子R702変異によるMYH9異常症の特徴2006
- Author(s)
  國島伸治
- Organizer
  第59回東海血栓症セミナー
- Place of Presentation
  名古屋
- Year and Date
  2006-10-21
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Utility of immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-IIA in the differential diagnosis of congenital macrothrombocytopenias.2006
- Author(s)
  Kunishima S
- Organizer
  XIXth International Symposium on Technological Innovations in Laboratory Hematology, ISLH2006 Amsterdam,
- Place of Presentation
  Amsterdam,the Netherlands
- Description
  「研究成果報告書概要(和文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Platelet size of Bernard-soulier syndrome and its carriers.2006
- Author(s)
  Kunishima S
- Organizer
  7th Congress of Japanese Society for Laboratory Hematology
- Place of Presentation
  Tokyo
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] Differential diagnosis of congenital macrothrombocytopenia
- Author(s)
  Shinji Kunishima
- Organizer
  8th Congress of the Asian-Pacific Society of Thrombosis and Hemostasis
- Place of Presentation
  Hanoi
- Year and Date
  2014-10-09 – 2014-10-11
- Invited
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] Differential expression of abnormal myosin in MYH9 disorders.
- Author(s)
  Kunishima S
- Organizer
  30th Annual meetind of Japanese Society on Thrombosis and Hemostatis.
- Description
  「研究成果報告書概要(欧文)」より
- Data Source
  KAKENHI-PROJECT-18591094
[Presentation] 巨核球特異的β1-tubulin異常は微小管構成阻害により胞体突起形成不全を来す
- Author(s)
  國島伸治　北村勝誠　西村智　鈴木英紀　今泉益栄　齋藤英彦
- Organizer
  第36回日本血栓止血学会学術集会
- Place of Presentation
  大阪
- Year and Date
  2014-05-29 – 2014-05-31
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] 先天性血小板減少症の鑑別診断
- Author(s)
  國島伸治
- Organizer
  北陸小児血液懇話会
- Place of Presentation
  金沢
- Invited
- Data Source
  KAKENHI-PROJECT-23591429
[Presentation] Molecular mechanisms for congenital macrothrombocytopenia
- Author(s)
  國島伸治
- Organizer
  第36回日本血栓止血学会学術集会
- Place of Presentation
  大阪
- Year and Date
  2014-05-29 – 2014-05-31
- Invited
- Data Source
  KAKENHI-PROJECT-26461413
[Presentation] MYH9異常症の体細胞モザイク
- Author(s)
  國島伸治　北村勝誠　松本多絵　関根孝司
- Organizer
  第15回日本検査血液学会学術集会
- Place of Presentation
  仙台
- Year and Date
  2014-07-20 – 2014-07-21
- Data Source
  KAKENHI-PROJECT-26461413

1. SEKINE Takashi (50255402)

# of Collaborated Projects: 2 results

# of Collaborated Products: 2 results
2. MATSUSHITA Tadashi (30314008)

# of Collaborated Projects: 2 results

# of Collaborated Products: 1 results
3. KURIHARA Hidetake (80311976)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
4. SAITO Hidehiko (20153819)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
5. HAMAGUCHI Motohiro (30393177)

# of Collaborated Projects: 2 results

# of Collaborated Products: 0 results
6. MIURA Kenichiro (70408483)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
7. YAMAZAKI Tomio (00282202)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
8. KOJIMA Tetsuhito (40161913)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
9. Kawai Tomoki (20631568)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
10. Ohara Osamu (20370926)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
11. Suzuki Hidenori (30158977)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
12. Oda Hirotsugu (20772239)

# of Collaborated Projects: 1 results

# of Collaborated Products: 1 results
13. Hiejima Eitaro (60773520)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
14. 西中村隆一 (70291309)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
15. 安彦行人 (40370944)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
16. 菅野純 (90186172)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
17. 安冨素子 (80554526)

# of Collaborated Projects: 1 results

# of Collaborated Products: 0 results
18. NAKAGAWA Kenji

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
19. NAMBA Kazunori

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
20. TAKAGI Akira

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
21. KANEKO Shin

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
22. NISHIMURA Satoshi

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
23. 戸田口淳也

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
24. 西小森隆太

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
25. 平家俊男

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
26. 小林正夫

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
27. 江藤浩之

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
28. 中内啓光

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
29. 長崎実佳

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results
30. 吉田健一

# of Collaborated Projects: 0 results

# of Collaborated Products: 2 results
31. 宮武聡子

# of Collaborated Projects: 0 results

# of Collaborated Products: 1 results

Kunishima Shinji 國島 伸治

國島 伸治 クニシマ シンジ

KUNISHIMA Shinji 國島 伸治

Research Projects

Research Products

Co-Researchers

Molecular mechanisms of ACTN1-macrothrombocytopeniaPrincipal Investigator

Principal Investigator

Project Period (FY)

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Review Section

Research Institution

アクチン架橋蛋白を介した免疫調節機構の解明

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ヒトiPSおよび新規遺伝子改変マウスを用いたネフローゼ症候群の病因解明

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Molecular pathogenesis of beta1 tubulin disordersPrincipal Investigator

Principal Investigator

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Investigation of pathology and development of specific medial care system and treatment associated with FLNA deficiency

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Characterization of a novel disease entity due to GPIIb/IIIa mutationsPrincipal Investigator

Principal Investigator

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Molecular analysis of the pathophysiology basis of nephrotic syndrome

Principal Investigator

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Molecular pathogenesis of MYH9 disordersPrincipal Investigator

Principal Investigator

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Elucidation of the mechanisms of giant platelet production in MYH9 disordersPrincipal Investigator

Principal Investigator

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Elucidation of molecular basis of May-Hegglin anomaly and its related disordes

Principal Investigator

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Research Institution

Establishment of differential diagnostic method for MYH9 disorders and characterization of mechanisms of leukocyte inclusion formationPrincipal Investigator

Principal Investigator

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Research Institution

[Book] 臨床に直結する血栓止血学2018

Author(s)

Total Pages

Publisher

ISBN

Data Source

[Book] 血液科研修ノート2016

Author(s)

Kunishima Shinji 國島伸治

國島伸治クニシマシンジ

KUNISHIMA Shinji 國島伸治

[Book] 小児慢性特定疾病―診断の手引き̶2015

[Book] 日本臨床　新領域別症候群シリーズNo22　血液症候群第2版2013