Zenichiro Kato

Gifu-shi, Japan

Last Updated: 09/26/2026

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Found 39 publications

Correction to: Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency.

Correction to: Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency.

Journal: Journal of clinical immunology

Published: August 14, 2024

Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency.

Exclusive Characteristics of the p.E555K Dominant-Negative Variant in Autosomal Dominant E47 Deficiency.

Journal: Journal of clinical immunology

Published: February 02, 2024

Monoallelic mutations in MMD2 cause autosomal dominant aggressive periodontitis.

Monoallelic mutations in MMD2 cause autosomal dominant aggressive periodontitis.

Journal: The Journal of experimental medicine

Published: October 17, 2023

Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan.

Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan.

Journal: Journal of clinical immunology

Published: August 18, 2022

Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases.

Novel STAT1 Variants in Japanese Patients with Isolated Mendelian Susceptibility to Mycobacterial Diseases.

Journal: Journal of clinical immunology

Published: March 30, 2022

Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica.

Novel nonsense mutation in the SLC39A4 gene in a Japanese boy with mild acrodermatitis enteropathica.

Journal: The Journal of dermatology

Published: April 09, 2021

Correction to: Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.

Correction to: Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.

Journal: Journal of clinical immunology

Published: March 11, 2021

Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.

Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.

Journal: Journal of clinical immunology

Published: October 09, 2020

IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation.

IRAK4 Deficiency Presenting with Anti-NMDAR Encephalitis and HHV6 Reactivation.

Journal: Journal of clinical immunology

Published: May 11, 2020

A Novel Homozygous Mutation Destabilizes IKKβ and Leads to Human Combined Immunodeficiency.

A Novel Homozygous Mutation Destabilizes IKKβ and Leads to Human Combined Immunodeficiency.

Journal: Frontiers in immunology

Published: December 04, 2019

Oral immunotherapy with antigenicity-modified casein induces desensitization in cow's milk allergy.

Oral immunotherapy with antigenicity-modified casein induces desensitization in cow's milk allergy.

Journal: Allergy

Published: February 08, 2019

An innate interaction between IL-18 and the propeptide that inactivates its precursor form.

An innate interaction between IL-18 and the propeptide that inactivates its precursor form.

Journal: Scientific reports

Published: January 17, 2019

Showing 1-12 of 39

Last Updated: 09/26/2026