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Journal Articles

A Novel 2 Amino Acids Deletion in the Leucine Zipper Domain of C/EBPε Leads to Neutrophil-Specific Granule Deficiency (SGD)

Tadayuki Akagi, PhD, Taizo Wada, MD PhD, Masahiro Muraoka, MD, Tomoko Toma, MD, Kenzo Kaji, MD, Kazunaga Agematsu, MD, H. Phillip Koeffler, MD, Takashi Yokota, PhD, Akihiro Yachie, MD PhD

Blood (2014) 124 (21): 4101.

https://doi.org/10.1182/blood.V124.21.4101.4101

Published: 2014

Journal Articles

Expansion of Liver-Infiltrating CTL Clone In Concert with the Development of Hepatitis-Associated AA.

Yasuhiro Ikawa, MD, PhD, Ryosei Nishimura, MD, PhD, Shintaro Mase, MD, Rie Kuroda, MD, Raita Araki, MD, Hideaki Maeba, MD, Masaki Shimizu, MD, PhD, Taizo Wada, MD, PhD, Tomoko Toma, MD, PhD, Shoichi Koizumi, MD, PhD, Akihiro Yachie, MD, PhD

Blood (2010) 116 (21): 1159.

https://doi.org/10.1182/blood.V116.21.1159.1159

Published: 2010

Journal Articles

Detection of T lymphocytes with a second-site mutation in skin lesions of atypical X-linked severe combined immunodeficiency mimicking Omenn syndrome

Taizo Wada, Masahiro Yasui, Tomoko Toma, Yuko Nakayama, Mika Nishida, Masaki Shimizu, Michiko Okajima, Yoshihito Kasahara, Shoichi Koizumi, Masami Inoue, Keisei Kawa, Akihiro Yachie

Blood (2008) 112 (5): 1872–1875.

https://doi.org/10.1182/blood-2008-04-149708

Published: 2008

Journal Articles

Somatic revertant mosaicism in a patient with leukocyte adhesion deficiency type 1

Yumi Tone, Taizo Wada, Fumie Shibata, Tomoko Toma, Yoko Hashida, Yoshihito Kasahara, Shoichi Koizumi, Akihiro Yachie

Blood (2006) 109 (3): 1182–1184.

https://doi.org/10.1182/blood-2006-08-039057

Published: 2006

Journal Articles

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1- deficient severe combined immunodeficiency

Taizo Wada, Tomoko Toma, Hiroyuki Okamoto, Yoshihito Kasahara, Shoichi Koizumi, Kazunaga Agematsu, Hirokazu Kimura, Akira Shimada, Yasuhide Hayashi, Masahiko Kato, Akihiro Yachie

Blood (2005) 106 (6): 2099–2101.

https://doi.org/10.1182/blood-2005-03-0936

Published: 2005

Journal Articles

Oligoclonal Expansion of Revertant T Cells Leads to Omenn Syndrome in a Patient with RAG1-Deficient Severe Combined Immunodeficiency.

Taizo Wada, MD, Hiroyuki Okamoto, MD, Tomoko Toma, MD, Yoshihito Kasahara, MD, Shoichi Koizumi, MD, Masahiko Kato, MD, Akihiro Yachie, MD

Blood (2004) 104 (11): 1333.

https://doi.org/10.1182/blood.V104.11.1333.1333

Published: 2004

Journal Articles

CD8αα memory effector T cells descend directly from clonally expanded CD8α + β high TCRαβ T cells in vivo

Akihiro Konno, Kanae Okada, Kazunori Mizuno, Mika Nishida, Shuya Nagaoki, Tomoko Toma, Takahiro Uehara, Kazuhide Ohta, Yoshihito Kasahara, Hidetoshi Seki, Akihiro Yachie, Shoichi Koizumi

Blood (2002) 100 (12): 4090–4097.

https://doi.org/10.1182/blood-2002-04-1136

Published: 2002

NARROW

A Novel 2 Amino Acids Deletion in the Leucine Zipper Domain of C/EBPε Leads to Neutrophil-Specific Granule Deficiency (SGD)

Expansion of Liver-Infiltrating CTL Clone In Concert with the Development of Hepatitis-Associated AA.

Detection of T lymphocytes with a second-site mutation in skin lesions of atypical X-linked severe combined immunodeficiency mimicking Omenn syndrome

Somatic revertant mosaicism in a patient with leukocyte adhesion deficiency type 1

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1- deficient severe combined immunodeficiency

Oligoclonal Expansion of Revertant T Cells Leads to Omenn Syndrome in a Patient with RAG1-Deficient Severe Combined Immunodeficiency.

CD8αα memory effector T cells descend directly from clonally expanded CD8α + β high TCRαβ T cells in vivo

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ASH Publications

American Society of Hematology

A Novel 2 Amino Acids Deletion in the Leucine Zipper Domain of C/EBPε Leads to Neutrophil-Specific Granule Deficiency (SGD)

Expansion of Liver-Infiltrating CTL Clone In Concert with the Development of Hepatitis-Associated AA.

Detection of T lymphocytes with a second-site mutation in skin lesions of atypical X-linked severe combined immunodeficiency mimicking Omenn syndrome

Somatic revertant mosaicism in a patient with leukocyte adhesion deficiency type 1

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1- deficient severe combined immunodeficiency

Oligoclonal Expansion of Revertant T Cells Leads to Omenn Syndrome in a Patient with RAG1-Deficient Severe Combined Immunodeficiency.

CD8αα memory effector T cells descend directly from clonally expanded CD8α + β high TCRαβ T cells in vivo

Email alerts

ASH Publications

American Society of Hematology

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