תוצאות חיפוש - Shinji Kunishima

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  1. 1
    Linkage between the mechanisms of thrombocytopenia and thrombopoiesis

    Linkage between the mechanisms of thrombocytopenia and thrombopoiesis מאת Koji Eto, Shinji Kunishima

    יצא לאור 2016
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    Revisão
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  2. 2
    Mutation of the β1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly

    Mutation of the β1-tubulin gene associated with congenital macrothrombocytopenia affecting microtubule assembly מאת Shinji Kunishima, Ryōji Kobayashi, Tomohiko J. Itoh, Motohiro Hamaguchi, Hidehiko Saito

    יצא לאור 2008
    קבל טקסט מלא קבל טקסט מלא
    Artigo
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  3. 3
    Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders

    Diagnosis of inherited platelet disorders on a blood smear: a tool to facilitate worldwide diagnosis of platelet disorders מאת Andreas Greinacher, Alessandro Pecci, Shinji Kunishima, Karina Althaus, Paquita Nurden, Carlo L. Balduini, T. Bakchoul

    יצא לאור 2017
    קבל טקסט מלא קבל טקסט מלא
    Artigo
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  4. 4
    Missense Mutations of the Glycoprotein (GP) Ibβ Gene Impairing the GPIb α/β Disulfide Linkage in a Family With Giant Platelet Disorder

    Missense Mutations of the Glycoprotein (GP) Ibβ Gene Impairing the GPIb α/β Disulfide Linkage in a Family With Giant Platelet Disorder מאת Shinji Kunishima, José A. López, Sentaro Kobayashi, N. Imai, Tadashi Kamiya, Hidehiko Saito, Tomoki Naoe

    יצא לאור 1997
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    Artigo
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  5. 5
    Demonstration of novel gain‐of‐function mutations of αIIbβ3: association with macrothrombocytopenia and glanzmann thrombasthenia‐like phenotype

    Demonstration of novel gain‐of‐function mutations of αIIbβ3: association with macrothrombocytopenia and glanzmann thrombasthenia‐like phenotype מאת Hirokazu Kashiwagi, Shinji Kunishima, Kazunobu Kiyomizu, Yoshiro Amano, Hiroyuki Shimada, Masashi Morishita, Yuzuru Kanakura, Yoshiaki Tomiyama

    יצא לאור 2013
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    Artigo
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  6. 6
    Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations

    Immunofluorescence Analysis of Neutrophil Nonmuscle Myosin Heavy Chain-A in MYH9 Disorders: Association of Subcellular Localization with MYH9 Mutations מאת Shinji Kunishima, Tadashi Matsushita, Tetsuhito Kojima, Masahiro Sako, Fumihiro Kimura, Eun‐Kyeong Jo, Chikako Inoue, Tadashi Kamiya, Hidehiko Saito

    יצא לאור 2003
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    Artigo
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  7. 7
    Heterozygous ITGA2B R995W mutation inducing constitutive activation of the αIIbβ3 receptor affects proplatelet formation and causes congenital macrothrombocytopenia

    Heterozygous ITGA2B R995W mutation inducing constitutive activation of the αIIbβ3 receptor affects proplatelet formation and causes congenital macrothrombocytopenia מאת Shinji Kunishima, Hirokazu Kashiwagi, Makoto Otsu, Naoya Takayama, Koji Eto, Masafumi Onodera, Yuji Miyajima, Yasushi Takamatsu, Junji Suzumiya, Kousaku Matsubara, Yoshiaki Tomiyama, Hidehiko Saito

    יצא לאור 2011
    קבל טקסט מלא קבל טקסט מלא
    Artigo
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  8. 8
    Microtubule polyglutamylation and acetylation drive microtubule dynamics critical for platelet formation

    Microtubule polyglutamylation and acetylation drive microtubule dynamics critical for platelet formation מאת Juliette van Dijk, Guillaume Bompard, Julien Cau, Shinji Kunishima, Gabriel Rabeharivelo, Julio Mateos–Langerak, Chantal Cazevieille, Patricia Cavelier, Brigitte Boizet‐Bonhoure, Claude Delsert, Nathalie Morin

    יצא לאור 2018
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    Artigo
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  9. 9
    Congenital amegakaryocytic thrombocytopenia iPS cells exhibit defective MPL-mediated signaling

    Congenital amegakaryocytic thrombocytopenia iPS cells exhibit defective MPL-mediated signaling מאת Shinji Hirata, Naoya Takayama, Ryoko Jono-Ohnishi, Hiroshi Endô, Sou Nakamura, Takeaki Dohda, Masanori Nishi, Yuhei Hamazaki, Eiichi Ishii, Shin Kaneko, Makoto Otsu, Hiromitsu Nakauchi, Shinji Kunishima, Koji Eto

    יצא לאור 2013
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    Artigo
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  10. 10
    Thrombosis from a Prothrombin Mutation Conveying Antithrombin Resistance

    Thrombosis from a Prothrombin Mutation Conveying Antithrombin Resistance מאת Yuhri Miyawaki, Atsuo Suzuki, Junko Fujita, Asuka Maki, Eriko Okuyama, Moe Murata, Akira Takagi, Takashi Murate, Shinji Kunishima, Michio Sakai, Kohji Okamoto, Tadashi Matsushita, Tomoki Naoe, Hidehiko Saito, Tetsuhito Kojima

    יצא לאור 2012
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    Artigo
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  11. 11
    IL-1α induces thrombopoiesis through megakaryocyte rupture in response to acute platelet needs

    IL-1α induces thrombopoiesis through megakaryocyte rupture in response to acute platelet needs מאת Satoshi Nishimura, Masao Nagasaki, Shinji Kunishima, Akira Sawaguchi, Asuka Sakata, Hiroyasu Sakaguchi, Tsukasa Ohmori, Ichiro Manabe, Joseph E. Italiano, Tomiko Ryu, Naoya Takayama, Issei Komuro, Takashi Kadowaki, Koji Eto, Ryozo Nagai

    יצא לאור 2015
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    Artigo
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  12. 12
    ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization

    ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization מאת Roberta Bottega, Caterina Marconi, Michela Faleschini, Gabriele Baj, Claudia Cagioni, Alessandro Pecci, Tommaso Pippucci, Ugo Ramenghi, Simonetta Pardini, Loretta Ngu, Carlo Baronci, Shinji Kunishima, Carlo L. Balduini, Marco Seri, Anna Savoia, Patrizia Noris

    יצא לאור 2014
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    Artigo
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  13. 13
    Identification of six novel MYH9 mutations and genotype–phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions

    Identification of six novel MYH9 mutations and genotype–phenotype relationships in autosomal dominant macrothrombocytopenia with leukocyte inclusions מאת Shinji Kunishima, Tadashi Matsushita, Toshiya Kojima, N Amemiya, Y. M. Choi, Naoki Hosaka, M. Inoue, Jung Yh, S Mamiya, Kiyoshi Matsumoto, Yuji Miyajima, Guolong Zhang, Changgeng Ruan, Kazuto Saito, K S Song, H.-J. Yoon, T. Kamiya, Hajime Saito

    יצא לאור 2001
    קבל טקסט מלא קבל טקסט מלא
    Artigo
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  14. 14
    ACTN1 Mutations Cause Congenital Macrothrombocytopenia

    ACTN1 Mutations Cause Congenital Macrothrombocytopenia מאת Shinji Kunishima, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Masashi Sanada, Hideki Muramatsu, Kenichi Chiba, Hiroko Tanaka, Kôji Miyazaki, Michio Sakai, Masatoshi Ohtake, Ryōji Kobayashi, Akihiro Iguchi, Gen Niimi, Makoto Otsu, Yoshiyuki Takahashi, Satoru Miyano, Hidehiko Saito, Seiji Kojima, Seishi Ogawa

    יצא לאור 2013
    קבל טקסט מלא
    Artigo
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  15. 15
    Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease

    Patients with Epstein–Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease מאת Takashi Sekine, Mutsuko Konno, Satoshi Sasaki, Suzuko Moritani, Takuma Miura, Wai-shan Wong, Hisanori Nishio, Toshihiro Nishiguchi, Miyako Yoshinari Ohuchi, Shigeru Tsuchiya, Takeshi Matsuyama, Hirokazu Kanegane, Komei Ida, Kenichiro Miura, Yutaka Harita, Motoshi Hattori, Shigeru Horita, Takashi Igarashi, Hidehiko Saito, Shinji Kunishima

    יצא לאור 2010
    קבל טקסט מלא קבל טקסט מלא
    Artigo
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  16. 16
    GPIbα is required for platelet-mediated hepatic thrombopoietin generation

    GPIbα is required for platelet-mediated hepatic thrombopoietin generation מאת Miao Xu, June Li, Miguel A. D. Neves, Guangheng Zhu, Naadiya Carrim, Ruoying Yu, Sahil Gupta, John C. Marshall, Ori D. Rotstein, Jun Peng, Ming Hou, Shinji Kunishima, Jerry Ware, Donald R. Branch, Alan H. Lazarus, Zaverio M. Ruggeri, John Freedman, Heyu Ni

    יצא לאור 2018
    קבל טקסט מלא קבל טקסט מלא
    Artigo
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  17. 17
    Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders

    Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders מאת Patrizia Noris, Ginevra Biino, Alessandro Pecci, Elisa Civaschi, Anna Savoia, Marco Seri, Federica Melazzini, Giuseppe Loffredo, Giovanna Russo, Valeria Bozzi, Lucia Dora Notarangelo, Paolo Gresele, Paula G. Heller, Núria Pujol‐Moix, Shinji Kunishima, Marco Cattaneo, James B. Bussel, Erica De Candia, Claudia Cagioni, Ugo Ramenghi, Serena Barozzi, Fabrizio Fabris, Carlo L. Balduini

    יצא לאור 2014
    קבל טקסט מלא
    Artigo
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  18. 18
    Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia

    Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia מאת Suthesh Sivapalaratnam, Sarah K. Westbury, Jonathan Stephens, Daniel Greene, Kate Downes, Anne M. Kelly, Claire Lentaigne, William J. Astle, Eric G. Huizinga, Paquita Nurden, Sofia Papadia, Kathelijne Peerlinck, Christopher J. Penkett, David J. Perry, Catherine Roughley, Ilenia Simeoni, Kathleen Stirrups, Daniel P. Hart, Robert C. Tait, Andrew Mumford, Michael Laffan, Kathleen Freson, Willem H. Ouwehand, Shinji Kunishima, Ernest Turro

    יצא לאור 2016
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    Artigo
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  19. 19
    Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes

    Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes מאת Hideki Muramatsu, Yusuke Okuno, Kenichi Yoshida, Yuichi Shiraishi, Sayoko Doisaki, Atsushi Narita, Hirotoshi Sakaguchi, Nozomu Kawashima, Xinan Wang, Yinyan Xu, Kenichi Chiba, Hiroko Tanaka, Asahito Hama, Masashi Sanada, Yoshiyuki Takahashi, Hitoshi Kanno, Hiroki Yamaguchi, Shouichi Ohga, Atsushi Manabe, Hideo Harigae, Shinji Kunishima, Eiichi Ishii, Masao Kobayashi, Kenichi Koike, Kenichiro Watanabe, Etsuro Ito, Minoru Takata, Miharu Yabe, Seishi Ogawa, Satoru Miyano, Seiji Kojima

    יצא לאור 2017
    קבל טקסט מלא קבל טקסט מלא
    Artigo
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  20. 20
    Spectrum of the Mutations in Bernard-Soulier Syndrome

    Spectrum of the Mutations in Bernard-Soulier Syndrome מאת Anna Savoia, Shinji Kunishima, Daniela De Rocco, Barbara Zieger, Margaret L. Rand, Núria Pujol‐Moix, Ümran Çalışkan, Hüseyin Tokgöz, Alessandro Pecci, Patrizia Noris, Alok Srivastava, Christopher Wård, Marie‐Christine Morel‐Kopp, Marie‐Christine Alessi, Sylvia Bellucci, Philippe Beurrier, Emmanuel de Maistre, Rémi Favier, Nathalie Hézard, Marie-Françoise Hurtaud-Roux, Véronique Latger‐Cannard, Cécile Lavenu‐Bombled, Valérie Proulle, Sandrine Meunier, Claude Négrier, Alan T. Nurden, Hanitra Randrianaivo, Fabrizio Fabris, Helen Platokouki, Nurit Rosenberg, Basma HadjKacem, Paula G. Heller, Mehran Karimi, Carlo L. Balduini, Annalisa Pastore, François Lanza

    יצא לאור 2014
    קבל טקסט מלא
    Revisão
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