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Publications by Naoe Kaneko

Novel Heterozygous C243Y A20/Tnfaip3 Gene Mutation Is Responsible for Chronic Inflammation in Autosomal-Dominant Behçet's Disease

RMD Open

English

The Role of Interleukin-1 in General Pathology

Inflammation and Regeneration

Allergy

Immunology

2019

English

Related publications

Juvenile Onset Autoinflammatory Disease Due to a Novel Mutation in TNFAIP3 (A20)

Arthritis Research & Therapy

2018

English

A Novel Heterozygous Mutation in Cardiac Calsequestrin Causes Autosomal Dominant Catecholaminergic Polymorphic Ventricular Tachycardia

Heart Rhythm

Cardiovascular Medicine

Physiology

Cardiology

2016

English

A Patient With a Novel Gene Mutation Leading to Autosomal Dominant Polycystic Kidney Disease

Clinical Journal of the American Society of Nephrology

Intensive Care Medicine

2017

English

Haploinsufficiency of TNFAIP3 ( A20 ) by Germline Mutation Is Involved in Autoimmune Lymphoproliferative Syndrome

Journal of Allergy and Clinical Immunology

Allergy

Immunology

2017

English

a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family

G3: Genes, Genomes, Genetics

English

A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

BioMed Research International

English

OPA3 Gene Mutations Responsible for Autosomal Dominant Optic Atrophy and Cataract

Journal of Medical Genetics

Genetics

2004

English

A Rhodopsin Gene Mutation Responsible for Autosomal Dominant Retinitis Pigmentosa Results in a Protein That Is Defective in Localization to the Photoreceptor Outer Segment

Journal of Neuroscience

Neuroscience

1994

English

A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome

Molecular Medicine Reports

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Naoe Kaneko

Novel Heterozygous C243Y A20/Tnfaip3 Gene Mutation Is Responsible for Chronic Inflammation in Autosomal-Dominant Behçet's Disease

The Role of Interleukin-1 in General Pathology

Related publications

Juvenile Onset Autoinflammatory Disease Due to a Novel Mutation in TNFAIP3 (A20)

A Novel Heterozygous Mutation in Cardiac Calsequestrin Causes Autosomal Dominant Catecholaminergic Polymorphic Ventricular Tachycardia

A Patient With a Novel Gene Mutation Leading to Autosomal Dominant Polycystic Kidney Disease

Haploinsufficiency of TNFAIP3 ( A20 ) by Germline Mutation Is Involved in Autoimmune Lymphoproliferative Syndrome

a Novel HSF4 Gene Mutation Causes Autosomal-Dominant Cataracts in a Chinese Family

A Novel Heterozygous Missense Mutation in GNAT1 Leads to Autosomal Dominant Riggs Type of Congenital Stationary Night Blindness

OPA3 Gene Mutations Responsible for Autosomal Dominant Optic Atrophy and Cataract

A Rhodopsin Gene Mutation Responsible for Autosomal Dominant Retinitis Pigmentosa Results in a Protein That Is Defective in Localization to the Photoreceptor Outer Segment

A Novel FBN1 Mutation Causes Autosomal Dominant Marfan Syndrome