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Journal Articles

Novel Heterozygous Mutation 572insA in TACI Identified in a Patient with Selective IgA Deficiency.

Satoshi Okada, MD, PhD, Teruyuki Kajiume, MD, PhD, Miyuki Tsumura, MSc, Kenichiro Shirao, MD, Yoshinori Ohno, MSc, Shin’ichiro Yasunaga, MD, PhD, Motoaki Ohtsubo, PhD, Mostafa Mofamed Sira, Hirokazu Kanegane, MD, PhD, Toshio Miyawaki, MD, PhD, Yoshihiro Takihara, MD, PhD, Masao Kobayashi, MD, PhD

Blood (2008) 112 (11): 1473.

https://doi.org/10.1182/blood.V112.11.1473.1473

Published: 2008

Journal Articles

Rapid detection of intracellular SH2D1A protein in cytotoxic lymphocytes from patients with X-linked lymphoproliferative disease and their family members

Yasuhiro Tabata, Joyce Villanueva, Susan Molleran Lee, Kejian Zhang, Hirokazu Kanegane, Toshio Miyawaki, Janos Sumegi, Alexandra H. Filipovich

Blood (2005) 105 (8): 3066–3071.

https://doi.org/10.1182/blood-2004-09-3651

Published: 2005

Journal Articles

Rapid Detection of SAP Deficiency in Cytotoxic Lymphocytes from Patients with X-Linked Lymphoproliferative Disease and Their Family Members.

Yasuhiro Tabata, MD, Joyce Villanueva, BS, Susan M. Lee, BS, Kejian Zhang, MD, Hirokazu Kanegane, MD, Toshio Miyawaki, MD, Janos Sumegi, MD, Alexandra H. Filipovich, MD

Blood (2004) 104 (11): 3846.

https://doi.org/10.1182/blood.V104.11.3846.3846

Published: 2004

Journal Articles

Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivation

Hidetoshi Takada, Hirokazu Kanegane, Akihiko Nomura, Ken Yamamoto, Kenji Ihara, Yasuhiko Takahashi, Satoshi Tsukada, Toshio Miyawaki, Toshiro Hara

Blood (2004) 103 (1): 185–187.

https://doi.org/10.1182/blood-2003-06-1964

Published: 2004

Journal Articles

SH2D1A mutations in Japanese males with severe Epstein-Barr virus–associated illnesses

Ryo Sumazaki, Hirokazu Kanegane, Maki Osaki, Takashi Fukushima, Masahiro Tsuchida, Hiroyoshi Matsukura, Kentaro Shinozaki, Hiroshi Kimura, Akira Matsui, Toshio Miyawaki

Blood (2001) 98 (4): 1268–1270.

https://doi.org/10.1182/blood.V98.4.1268

Published: 2001

Journal Articles

Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway

Keiko Nomura, Hirokazu Kanegane, Hajime Karasuyama, Satoshi Tsukada, Kazunaga Agematsu, Gyokei Murakami, Satoru Sakazume, Masahiro Sako, Rieko Tanaka, Yoshinori Kuniya, Takuya Komeno, Shigehiko Ishihara, Keizo Hayashi, Tadamitsu Kishimoto, Toshio Miyawaki

Blood (2000) 96 (2): 610–617.

https://doi.org/10.1182/blood.V96.2.610

Published: 2000

Journal Articles

X-linked thrombocytopenia identified by flow cytometric demonstration of defective Wiskott-Aldrich syndrome protein in lymphocytes

Hirokazu Kanegane, Keiko Nomura, Toshio Miyawaki, Yoji Sasahara, Shin Kawai, Shigeru Tsuchiya, Gyokei Murakami, Takeshi Futatani, Hans D. Ochs

Blood (2000) 95 (3): 1110–1111.

https://doi.org/10.1182/blood.V95.3.1110

Published: 2000

Journal Articles

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

Takeshi Futatani, Toshio Miyawaki, Satoshi Tsukada, Shoji Hashimoto, Toshio Kunikata, Shigeyuki Arai, Masashi Kurimoto, Yo Niida, Hiroshi Matsuoka, Yukio Sakiyama, Tsutomu Iwata, Shigeru Tsuchiya, Osamu Tatsuzawa, Kazuyuki Yoshizaki, Tadamitsu Kishimoto

Blood (1998) 91 (2): 595–602.

https://doi.org/10.1182/blood.V91.2.595

Published: 1998

Journal Articles

Involvement of Reactive Oxygen Intermediates in Spontaneous and CD95(Fas/APO-1)–Mediated Apoptosis of Neutrophils

Yoshihito Kasahara, Kazuyuki Iwai, Akihiro Yachie, Kunio Ohta, Akihiro Konno, Hidetoshi Seki, Toshio Miyawaki, Noboru Taniguchi

Blood (1997) 89 (5): 1748–1753.

https://doi.org/10.1182/blood.V89.5.1748

Published: 1997

NARROW

Novel Heterozygous Mutation 572insA in TACI Identified in a Patient with Selective IgA Deficiency.

Rapid detection of intracellular SH2D1A protein in cytotoxic lymphocytes from patients with X-linked lymphoproliferative disease and their family members

Rapid Detection of SAP Deficiency in Cytotoxic Lymphocytes from Patients with X-Linked Lymphoproliferative Disease and Their Family Members.

Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivation

SH2D1A mutations in Japanese males with severe Epstein-Barr virus–associated illnesses

Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway

X-linked thrombocytopenia identified by flow cytometric demonstration of defective Wiskott-Aldrich syndrome protein in lymphocytes

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

Involvement of Reactive Oxygen Intermediates in Spontaneous and CD95(Fas/APO-1)–Mediated Apoptosis of Neutrophils

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American Society of Hematology

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ASH Publications

American Society of Hematology

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