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Takeshi Futatani

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Shihomi Ina; Shoetsu Shimura; Hiroyuki Higashiyama; Noboru Igarashi; Shuhei Fujita; Takeshi Futatani; Nobuko Hashida; Kiyoshi Hatasaki
Left atrium thrombus in an extremely low-birthweight infant with late-onset circulatory dysfunction.
Shuhei Fujita; Takeshi Futatani; Hiroyuki Higashiyama; Noboru Igarashi; Shihomi Ina; Uta Koura; Taichi Nakamura; Shoetsu Shimura; Akiko Toga; Kiyoshi Hatasaki
Commotio Cordis presenting as a temporary complete atrioventricular block in a 2-year-old girl with congenitally corrected transposition of the great arteries.
Takashi Arai; Tadashi Ariga; Takeshi Futatani; Hirokazu Kanegane; Toshio Miyawaki; Hans D Ochs; Menno van Zelm; Masafumi Yamada; Meina Zhao; Tsutomu Oh-ishi
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes.

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All Publications

2012: Shihomi Ina; Shoetsu Shimura; Hiroyuki Higashiyama; Noboru Igarashi; Shuhei Fujita; Takeshi Futatani; Nobuko Hashida; Kiyoshi Hatasaki
Left atrium thrombus in an extremely low-birthweight infant with late-onset circulatory dysfunction.
Pediatrics international : official journal of the Japan Pediatric Society 2012;54(4):555-8.
2011: Shuhei Fujita; Takeshi Futatani; Hiroyuki Higashiyama; Noboru Igarashi; Shihomi Ina; Uta Koura; Taichi Nakamura; Shoetsu Shimura; Akiko Toga; Kiyoshi Hatasaki
Commotio Cordis presenting as a temporary complete atrioventricular block in a 2-year-old girl with congenitally corrected transposition of the great arteries.
Pediatric cardiology 2011;32(7):1043-7.
2011: Takashi Arai; Tadashi Ariga; Takeshi Futatani; Hirokazu Kanegane; Toshio Miyawaki; Hans D Ochs; Menno van Zelm; Masafumi Yamada; Meina Zhao; Tsutomu Oh-ishi
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes.
Journal of human genetics 2011;56(8):577-82.
2009: Mostafa Sira; Taketoshi Yoshida; Makoto Takeuchi; Yoshinori Kashiwayama; Takeshi Futatani; Hirokazu Kanegane; Akiko Sasahara; Yasunori Ito; Mineyuki Mizuguchi; Tsuneo Imanaka; Toshio Miyawaki
A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells.
International immunology 2009;21(9):1013-23.
2009: Kazuhiro Watabnabe; Keiichiro Uese; Osamu Higuchi; Takeshi Futatani; Naoki Yoshimura; Tsuneyuki Nakamura; Fukiko Ichida
Three-dimensional computed tomographic findings of bilateral tracheal bronchus.
Pediatric cardiology 2009;30(1):87-8.
2008: Dong-Min Shin; Eun-Kyeong Jo; Hirokazu Kanegane; Takeshi Futatani; Meina Zhao; Chang-Hwa Song; Atsushi Yamagishi; Toshio Miyawaki
Transcriptional regulatory defects in the first intron of Bruton's tyrosine kinase.
Pediatrics international : official journal of the Japan Pediatric Society 2008;50(6):801-5.
2008: Jiro Ogawa; Hirokazu Kanegane; Koichi tsuneyama; Rika Kanezaki; Takeshi Futatani; Keiko Nomura; Shin Ishizawa; Masakiyo Sasahara; Etsuro Ito; Toshio Miyawaki
Platelet-derived growth factor may be associated with fibrosis in a Down syndrome patient with transient myeloproliferative disorder.
European journal of haematology 2008;81(1):58-64.
2008: Lishen Shan; Naomasa Makita; Yanlin Xing; Sayake Watanabe; Takeshi Futatani; Fei Ye; Kazuyoshi Saito; Keijiro Ibuki; Kazuhiro Watanabe; Keiichi Hirono; Keiichiro Uese; Fukiko Ichida; Toshio Miyawaki; Hideki Origasa; Neil E Bowles; Jeffrey A Towbin
SCN5A variants in Japanese patients with left ventricular noncompaction and arrhythmia.
Molecular genetics and metabolism 2008;93(4):468-74.
2008: Takeshi Futatani; Eiji Nii; Makoto Obata; Fukiko Ichida; Yoshie Okabe; Hirokazu Kanegane; Toshio Miyawaki
Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease.
Pediatrics international : official journal of the Japan Pediatric Society 2008;50(1):116-8.
2008: Hiromichi Taneichi; Hirokazu Kanegane; Mostafa Sira; Takeshi Futatani; Kazunaga Agematsu; Masahiro Sako; Hideo Kaneko; Naomi Kondo; Tsuneyasu Kaisho; Toshio Miyawaki
Toll-like receptor signaling is impaired in dendritic cells from patients with X-linked agammaglobulinemia.
Clinical immunology (Orlando, Fla.) 2008;126(2):148-54.
2007: Tatsuya Fuchizawa; Yuichi Adachi; Yasunori Ito; Hiroyuki Higashiyama; Hirokazu Kanegane; Takeshi Futatani; Ichiro Kobayashi; Yoshiro Kamachi; Tatsuo Sakamoto; Ikuya Tsuge; Hiroshi Tanaka; Alison H Banham; Hans D Ochs; Toshio Miyawaki
Developmental changes of FOXP3-expressing CD4+CD25+ regulatory T cells and their impairment in patients with FOXP3 gene mutations.
Clinical immunology (Orlando, Fla.) 2007;125(3):237-46.
2007: H Kanegane; Kazunaga Agematsu; Takeshi Futatani; Mostafa Sira; K Suga; T Sekiguchi; Menno van Zelm; T Miyawaki
Novel mutations in a Japanese patient with CD19 deficiency.
Genes and immunity 2007;8(8):663-70.
2007: Anna Sedivá; C I Edvard Smith; A Charlotta Asplund; Jan Hadac; Ales Janda; Jirí Zeman; Hana Hansíková; Lenka Dvoráková; Lenka Mrázová; Sirje Velbri; Carla Koehler; Karin Roesch; Kathleen E Sullivan; Takeshi Futatani; Hans D Ochs
Contiguous X-chromosome deletion syndrome encompassing the BTK, TIMM8A, TAF7L, and DRP2 genes.
Journal of clinical immunology 2007;27(6):640-6.
2007: Lida Atarod; Asghar Aghamohammadi; Mostafa Moin; Hiro Kanegane; Nima Rezaei; Kiara Rezaei Kalantari; Ali Akbar Amirzagar; Takeshi Futatani; Miyawaki Miyawaki
Successful management of neutropenia in a patient with CD40 ligand deficiency by immunoglobulin replacement therapy.
Iranian journal of allergy, asthma, and immunology 2007;6(1):37-40.
2006: Keiichi Hirono; Dirk Foell; Yanlin Xing; Sachiko Miyagawa-Tomita; Fei Ye; Martina Ahlmann; Thomas Vogl; Takeshi Futatani; Chen Rui; Xianyi Yu; Kazuhiro Watanabe; Sayaka Wanatabe; Shinichi Tsubata; Keiichiro Uese; Ikuo Hashimoto; Fukiko Ichida; Makoto Nakazawa; Johannes Roth; Toshio Miyawaki
Expression of myeloid-related protein-8 and -14 in patients with acute Kawasaki disease.
Journal of the American College of Cardiology 2006;48(6):1257-64.
2006: Hiromichi Taneichi; Hirokazu Kanegane; Takeshi Futatani; Keisuke Otsubo; Keiko Nomura; Yuya Sato; Asahito Hama; Seiji Kojima; Urara Kohdera; Takahide Nakano; Hiroki Hori; Hisashi Kawashima; Yoko Inoh; Junji Kamizono; Naoto Adachi; Yuko Osugi; Haruo Mizuno; Noriko Hotta; Hiroshi Yoneyama; Eiji Nakashima; Shiro Ikegawa; Toshio Miyawaki
Clinical and genetic analyses of presumed Shwachman-Diamond syndrome in Japan.
International journal of hematology 2006;84(1):60-2.
2006: Yanlin Xing; Fukiko Ichida; Taro Matsuoka; Takeshi Isobe; Yumiko Ikemoto; Takashi Higaki; Tohru Tsuji; Noriyuki Haneda; Atsushi Kuwabara; Rui Chen; Takeshi Futatani; Shinichi Tsubata; Sayaka Watanabe; Kazuhiro Watanabe; Keiichi Hirono; Keiichiro Uese; Toshio Miyawaki; Karla R Bowles; Neil E Bowles; Jeffrey A Towbin
Genetic analysis in patients with left ventricular noncompaction and evidence for genetic heterogeneity.
Molecular genetics and metabolism 2006;88(1):71-7.
2005: Hirokazu Kanegane; Hiromichi Taneichi; Keiko Nomura; Takeshi Futatani; Toshio Miyawaki
Severe neutropenia in Japanese patients with x-linked agammaglobulinemia.
Journal of clinical immunology 2005;25(5):491-5.
2005: Naoko Tanaka-Kitajima; Naomi Sugaya; Takeshi Futatani; Hirokazu Kanegane; Chizuko Suzuki; Makoto Oshiro; Masahiro Hayakawa; Masahide Futamura; Tsuneo Morishima; Hiroshi Kimura
Ganciclovir therapy for congenital cytomegalovirus infection in six infants.
The Pediatric infectious disease journal 2005;24(9):782-5.
2005: Takeshi Futatani; Hirokazu Kanegane; Toshio Miyawaki
[Primary immunodeficiency diseases].
Nihon rinsho. Japanese journal of clinical medicine 2005;63 Suppl 5():559-64.
2005: Hirokazu Kanegane; Yoshikiyo Ito; Koichi Ohshima; Takeshi Shichijo; Kunio Tomimasu; Keiko Nomura; Takeshi Futatani; Ryo Sumazaki; Toshio Miyawaki
X-linked lymphoproliferative syndrome presenting with systemic lymphocytic vasculitis.
American journal of hematology 2005;78(2):130-3.
2004: Asghar Aghamohammadi; Nima Parvaneh; Hirokazu Kanegana; Mostafa Moin; Ali Akbar Amirzargar; Abolhassan Farhoudi; Zahra Pourpak; Masoud Movahedi; Mohammad Gharagozlou; Nima Rezaei; Takeshi Futatani; Toshio Miyawaki
Screening of the Bruton Tyrosine Kinase (BTK) Gene Mutations in 13 Iranian Patients with Presumed X-Linked Agammaglobulinemia.
Iranian journal of allergy, asthma, and immunology 2004;3(4):175-9.
2004: Takenori Mikami; Seiji Hayasaka; Yasunori Nagaki; Shuichiro Yanagisawa; Takeshi Futatani; Yasuo Takano
Congenital corneal staphyloma associated with aphakia.
Journal of pediatric ophthalmology and strabismus 2004;41(3):180-2.
2004: Jiro Ogawa; Akiko Sasahara; Taketoshi Yoshida; Mostafa Sira; Takeshi Futatani; Hirokazu Kanegane; Toshio Miyawaki
Role of transforming growth factor-beta in breast milk for initiation of IgA production in newborn infants.
Early human development 2004;77(1-2):67-75.
2003: Satomi Miyazaki; Hiroshi Tsuda; Masatoshi Sakai; Shinichi Hori; Yasushi Sasaki; Takeshi Futatani; Toshio Miyawaki; Shigeru Saito
Predominance of Th2-promoting dendritic cells in early human pregnancy decidua.
Journal of leukocyte biology 2003;74(4):514-22.
2003: Eun-Kyeong Jo; Takeshi Futatani; Hirokazu Kanegane; Takeo Kubota; Young-Ho Lee; Jin-A Jung; Chang-Hwa Song; Jeong-Kyu Park; Shigeaki Nonoyama; Toshio Miyawaki
Mutational analysis of the WASP gene in 2 Korean families with Wiskott-Aldrich syndrome.
International journal of hematology 2003;78(1):40-4.
2003: Shinichiro Hirokawa; Hideyuki Uotani; Hideo Okami; Kazuhiro Tsukada; Takeshi Futatani; Ikuo Hashimoto
A case of congenital midline cervical cleft with congenital heart disease.
Journal of pediatric surgery 2003;38(7):1099-101.
2003: Shinichiro Hirokawa; Hideyuki Uotani; Takeshi Futatani; Y Sasaki; J Ogawa; M Sakai; Kazuhiro Tsukada; S Saito
A case of body stalk anomaly arising in the second baby of a triplet pregnancy after in-vitro fertilization and embryo transfer.
Pediatric surgery international 2003;19(3):223-5.
2003: Hirokazu Kanegane; Maria Marluce dos Santos Vilela; Yue Wang; Takeshi Futatani; Hiroyoshi Matsukura; Toshio Miyawaki
Autoimmune lymphoproliferative syndrome presenting with glomerulonephritis.
Pediatric nephrology (Berlin, Germany) 2003;18(5):454-6.
2003: Cristián Rodríguez; Flavio Carrión; María Angélica Marinovic; Eduardo Chávez; Jessica Preisler; Francisco Pooley; Takeshi Futatani; Hans D Ochs
[X-linked hyper-IGM syndrome associated to sclerosing cholangitis and gallbladder neoplasm: clinical case].
Revista médica de Chile 2003;131(3):303-8.
2003: Eun-Kyeong Jo; Yue Wang; Hirokazu Kanegane; Takeshi Futatani; Chang-Hwa Song; Jeong-Kyu Park; Jung Soo Kim; Dong Soo Kim; Kang-Mo Ahn; Sang-Il Lee; Hyeon Jin Park; Youn Soo Hahn; Jae-Ho Lee; Toshio Miyawaki
Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients.
Journal of human genetics 2003;48(6):322-6.
2002: Sergio Massayuki Tani; Yue Wang; Hirokazu Kanegane; Takeshi Futatani; Jorge Pinto; Maria Marluce dos Santos Vilela; Toshio Miyawaki
Identification of mutations of Bruton's tyrosine kinase gene (BTK) in Brazilian patients with X-linked agammaglobulinemia.
Human mutation 2002;20(3):235-6.
2002: Hirokazu Kanegane; Keiko Nomura; Takeshi Futatani; Toshio Miyawaki
[Intravenous immunoglobulin replacement therapy in X-linked agammaglobulinemia].
Nihon Rinshō Men'eki Gakkai kaishi = Japanese journal of clinical immunology 2002;25(4):337-43.
2002: Kazunaga Agematsu; Takeshi Futatani; Sho Hokibara; Norimoto Kobayashi; Masaya Takamoto; Satoshi Tsukada; Harumi Suzuki; Shigeo Koyasu; Toshio Miyawaki; Kazuo Sugane; Atsushi Komiyama; Hans D Ochs
Absence of memory B cells in patients with common variable immunodeficiency.
Clinical immunology (Orlando, Fla.) 2002;103(1):34-42.
2002: Yue Wang; Hirokazu Kanegane; Ozden Sanal; Ilhan Tezcan; Fügen Ersoy; Takeshi Futatani; Toshio Miyawaki
Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia.
American journal of medical genetics 2002;108(4):333-6.
2001: Hirokazu Kanegane; Takeshi Futatani; Yue Wang; Keiko Nomura; K Shinozaki; Hiroyoshi Matsukura; T Kubota; Satoshi Tsukada; Toshio Miyawaki
Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis.
The Journal of allergy and clinical immunology 2001;108(6):1012-20.
2001: Yue Wang; Hirokazu Kanegane; Ozden Sanal; F Ersoy; Ilhan Tezcan; Takeshi Futatani; Satoshi Tsukada; Toshio Miyawaki
Bruton tyrosine kinase gene mutations in Turkish patients with presumed X-linked agammaglobulinemia.
Human mutation 2001;18(4):356.
2001: Takeshi Futatani; C Watanabe; Y Baba; Satoshi Tsukada; Hans D Ochs
Bruton's tyrosine kinase is present in normal platelets and its absence identifies patients with X-linked agammaglobulinaemia and carrier females.
British journal of haematology 2001;114(1):141-9.
2001: Yuji Hamamichi; Fukiko Ichida; Xianyi Yu; Keiichi Hirono; Keiichiro Uese; Ikuo Hashimoto; Shinichi Tsubata; T Yoshida; Takeshi Futatani; Hirokazu Kanegane; Toshio Miyawaki
Neutrophils and mononuclear cells express vascular endothelial growth factor in acute Kawasaki disease: its possible role in progression of coronary artery lesions.
Pediatric research 2001;49(1):74-80.
2000: Toshio Miyawaki; Hirokazu Kanegane; Takeshi Futatani
[Agammaglobulinemia as early B cell defects].
Nihon Rinshō Men'eki Gakkai kaishi = Japanese journal of clinical immunology 2000;23(5):435-44.
2000: Hirokazu Kanegane; Satoshi Tsukada; T Iwata; Takeshi Futatani; Keiko Nomura; J Yamamoto; T Yoshida; Kazunaga Agematsu; Atsushi Komiyama; Toshio Miyawaki
Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese Immunodeficiency Registry.
Clinical and experimental immunology 2000;120(3):512-7.
1999: Shouji Hashimoto; T Miyawaki; Takeshi Futatani; Hirokazu Kanegane; Kazuhiro Usui; T Nukiwa; S Namiuchi; M Matsushita; Tomoki Yamadori; Masaki Suemura; Tadamitsu Kishimoto; Satoshi Tsukada
Atypical X-linked agammaglobulinemia diagnosed in three adults.
Internal medicine (Tokyo, Japan) 1999;38(9):722-5.
1998: Takeshi Futatani; Toshio Miyawaki; Satoshi Tsukada; Shouji Hashimoto; T Kunikata; S Arai; M Kurimoto; Yo Niida; H Matsuoka; Yukio Sakiyama; T Iwata; S Tsuchiya; O Tatsuzawa; K Yoshizaki; Tadamitsu Kishimoto
Deficient expression of Bruton's tyrosine kinase in monocytes from X-linked agammaglobulinemia as evaluated by a flow cytometric analysis and its clinical application to carrier detection.
Blood 1998;91(2):595-602.