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The Behavior and Acrosomal Status of Mouse Spermatozoa In Vitro, and Within the Oviduct During Fertilization after Natural Mating

Biology of reproduction, 2016-09, Vol.95 (3), p.50-50

2016

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Magnetic structure and crystal field excitations of NdOs2Al10: a neutron scattering study

Journal of physics. Condensed matter, 2021-04, Vol.33 (18)

2021

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Simple and low-cost tabletop NMR system for chemical-shift-resolution spectra measurements

Journal of magnetic resonance (1997), 2018-09, Vol.294, p.128-132

2018

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Epithelioid cell granuloma formation in CARD14‐associated papulosquamous eruptions

Journal of the European Academy of Dermatology and Venereology, 2022-05, Vol.36 (5), p.e369-e371

2022

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Ferromagnetism and re-entrant spin-glass transition in quasicrystal approximants Au-SM-Gd (SM = Si, Ge)

Journal of physics. Condensed matter, 2013-10, Vol.25 (42), p.426004-426004

2013

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Pressure-induced ferromagnetic order in the weak ferromagnet YbRhSb

Journal of physics. Conference series, 2009-03, Vol.150 (4), p.042223

2009

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A patient with CARD14‐associated papulosquamous eruptions showing atopic dermatitis‐like features

Journal of the European Academy of Dermatology and Venereology, 2021-01, Vol.35 (1), p.e58-e59

2021

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Image Gallery: Palmoplantar hyperkeratosis in dermatomyositis with anti‐PM/Scl antibodies

British journal of dermatology (1951), 2017-05, Vol.176 (5), p.e94-e94

2017

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A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis

British journal of dermatology (1951), 2012-09, Vol.167 (3), p.699-701

2012

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Rapid increase of serum anti‐MDA‐5 antibodies and exacerbation of clinically amyopathic dermatomyositis/interstitial lung disease

Journal of the European Academy of Dermatology and Venereology, 2017-01, Vol.31 (1), p.e43-e44

2017

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Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children

British journal of dermatology (1951), 2018-07, Vol.179 (1), p.190-191

2018

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A case of late middle age‐onset recurrent rheumatic fever

Clinical and experimental dermatology, 2020-07, Vol.45 (5), p.595-596

2020

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Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations

Journal of the European Academy of Dermatology and Venereology, 2022-03, Vol.36 (3), p.e215-e218

2022

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Mild Hailey–Hailey disease cases with aberrant splicing variants of ATP2C1 successfully controlled with excimer light

Journal of the European Academy of Dermatology and Venereology, 2018-11, Vol.32 (11), p.e413-e416

2018

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MEDNIK‐like syndrome due to compound heterozygous mutations in AP1B1

Journal of the European Academy of Dermatology and Venereology, 2021-05, Vol.35 (5), p.e345-e347

2021

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High concomitance of disease marker autoantibodies in anti-DFS70/LEDGF autoantibody–positive patients with autoimmune rheumatic disease

Lupus, 2008-03, Vol.17 (3), p.171-176

2008

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A Japanese Case of Galli-Galli Disease due to a Previously Unreported POGLUT1 Mutation

Acta dermato-venereologica, 2019-04, Vol.99 (4), p.458-459

2019

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Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A–I editing efficiency of ADAR1 mutants and phenotype expression

British journal of dermatology (1951), 2018-08, Vol.179 (2), p.509-511

2018

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Hailey‐Hailey disease due to ATP2C1 splice site mutation, successfully treated with minocycline hydrochloride

Journal of the European Academy of Dermatology and Venereology, 2018-01, Vol.32 (1), p.e19-e20

2018

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Common and Specific Associations of Anti-SSA/Ro60 and Anti-Ro52/TRIM21 Antibodies in Systemic Lupus Erythematosus

TheScientificWorld, 2013-01, Vol.2013 (2013), p.1-8

2013

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Muon-spin-relaxation and inelastic neutron scattering investigations of the caged-type Kondo semimetals: CeT2Al10 (T = Fe, Ru and Os)

Physica scripta, 2013-12, Vol.88 (6)

2013

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Acrodermatitis continua of Hallopeau with dense infiltration of IgG4‐positive cells in the lesional dermis

British journal of dermatology (1951), 2019-04, Vol.180 (4), p.941-942

2019

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MEDNIK‐like syndrome due to compound heterozygous mutations in AP1B1

Journal of the European Academy of Dermatology and Venereology, 2021-05, Vol.35 (5)

2021

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Dilution effects on the antiferromagnetic Kondo semiconductor CeOs2Al10

Journal of physics. Conference series, 2017-04, Vol.807 (2)

2017

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Dyschromatosis symmetrica hereditaria with chilblains due to a novel two‐amino‐acid deletion in the double‐stranded RNA‐binding domain of ADAR1

Journal of the European Academy of Dermatology and Venereology, 2018-10, Vol.32 (10), p.e394-e396

2018

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The Behavior and Acrosomal Status of Mouse Spermatozoa In Vitro, and Within the Oviduct During Fertilization after Natural Mating

Magnetic structure and crystal field excitations of NdOs2Al10: a neutron scattering study

Simple and low-cost tabletop NMR system for chemical-shift-resolution spectra measurements

Epithelioid cell granuloma formation in CARD14‐associated papulosquamous eruptions

Ferromagnetism and re-entrant spin-glass transition in quasicrystal approximants Au-SM-Gd (SM = Si, Ge)

Pressure-induced ferromagnetic order in the weak ferromagnet YbRhSb

A patient with CARD14‐associated papulosquamous eruptions showing atopic dermatitis‐like features

Image Gallery: Palmoplantar hyperkeratosis in dermatomyositis with anti‐PM/Scl antibodies

A novel IL36RN/IL1F5 homozygous nonsense mutation, p.Arg10X, in a Japanese patient with adult-onset generalized pustular psoriasis

Rapid increase of serum anti‐MDA‐5 antibodies and exacerbation of clinically amyopathic dermatomyositis/interstitial lung disease

Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children

A case of late middle age‐onset recurrent rheumatic fever

Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations

Mild Hailey–Hailey disease cases with aberrant splicing variants of ATP2C1 successfully controlled with excimer light

MEDNIK‐like syndrome due to compound heterozygous mutations in AP1B1

High concomitance of disease marker autoantibodies in anti-DFS70/LEDGF autoantibody–positive patients with autoimmune rheumatic disease

A Japanese Case of Galli-Galli Disease due to a Previously Unreported POGLUT1 Mutation

Bilateral striatal necrosis and dyschromatosis symmetrica hereditaria: A–I editing efficiency of ADAR1 mutants and phenotype expression

Hailey‐Hailey disease due to ATP2C1 splice site mutation, successfully treated with minocycline hydrochloride

Common and Specific Associations of Anti-SSA/Ro60 and Anti-Ro52/TRIM21 Antibodies in Systemic Lupus Erythematosus

Muon-spin-relaxation and inelastic neutron scattering investigations of the caged-type Kondo semimetals: CeT2Al10 (T = Fe, Ru and Os)

Acrodermatitis continua of Hallopeau with dense infiltration of IgG4‐positive cells in the lesional dermis

MEDNIK‐like syndrome due to compound heterozygous mutations in AP1B1

Dilution effects on the antiferromagnetic Kondo semiconductor CeOs2Al10

Dyschromatosis symmetrica hereditaria with chilblains due to a novel two‐amino‐acid deletion in the double‐stranded RNA‐binding domain of ADAR1

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