Yoko Mizoguchi

Hiroshima University

Japan

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Articles (14)

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2025

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2025

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2025

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2025

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

Collaborators (15)

Hideki Yoshida

Assistant professor

Kyoto Prefectural University of Medicine

JAPAN

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Shun Ohki

Assistant Professor

Hiroshima University

JAPAN

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MARTA MURGIA

Assistant Professor

University of Padua

ITALY

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Yoshitaka Honda

特定助教 / Program-Specific Assistant Professor

Kyoto University

JAPAN

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Motoshi Sonoda

Kyushu University

JAPAN

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Shinji Matsuda

Hiroshima University

JAPAN

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Ejona Rusha

Head of Core Facility

Helmholtz Zentrum München

GERMANY

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Takaki Asano

Assistant professor

Hiroshima University

JAPAN

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Peng Zhang

Rockefeller University

UNITED STATES

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Shigeo Kure

JAPAN

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Tomoharu Yasuda

Professor

Hiroshima University

JAPAN

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Satoshi Okada

Professor

Hiroshima University

JAPAN

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Ralf Zimmer

Professor

Ludwig-Maximilians-Universität München

GERMANY

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Jean-Laurent Casanova

Levy Family Professor

Rockefeller University

UNITED STATES

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Takahiro Kamiya

Tokyo Medical and Dental University

JAPAN

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Yoko Mizoguchi

Research Interests

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Articles (14)

Fine mapping of heterozygous IL6ST nonsense variants underlying autosomal dominant hyper-IgE syndrome.

Multiple Hematopoietic Stem Cell Transplantations in Pediatric Acute Myeloid Leukemia: Prognostic Significance of Remission and Severe Sinusoidal Obstruction Syndrome

Monoallelic mutations in MMD2 cause autosomal dominant aggressive periodontitis

X-linked severe combined immunodeficiency with Down syndrome identified by newborn screening

Structural basis of spike RBM-specific human antibodies counteracting broad SARS-CoV-2 variants

A complementary approach for genetic diagnosis of inborn errors of immunity using proteogenomic analysis

Human RELA dominant-negative mutations underlie type I interferonopathy with autoinflammation and autoimmunity

Age‐specific incidence of joint disease in paediatric patients with haemophilia: A single‐centre real‐world outcome based on consecutive US examination

Analyzing mitochondrial respiration of human induced pluripotent stem cell-derived myeloid progenitors using Seahorse technology

Human genetic defects in SRP19 and SRPRA cause severe congenital neutropenia with distinctive proteome changes.

Neutralizing Type I Interferon Autoantibodies in Japanese Patients with Severe COVID-19

Human T-bet governs the generation of a distinct subset of CD11c<sup>high</sup>CD21<sup>low</sup> B cells.

HAX1-dependent control of mitochondrial proteostasis governs neutrophil granulocyte differentiation

Mendelian susceptibility to mycobacterial diseases: state of the art.

Collaborators (15)

Hideki Yoshida

Shun Ohki

MARTA MURGIA

Yoshitaka Honda

Motoshi Sonoda

Shinji Matsuda

Ejona Rusha

Takaki Asano

Peng Zhang

Shigeo Kure

Tomoharu Yasuda

Satoshi Okada

Ralf Zimmer

Jean-Laurent Casanova

Takahiro Kamiya

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