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Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome

Scientific reports, 2018-08, Vol.8 (1), p.12824-11, Article 12824

2018

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Studies on thermal and mechanical properties of polyimide–clay nanocomposites

Polymer (Guilford), 2001-04, Vol.42 (8), p.3399-3408

2001

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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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Novel Benzoxazine Monomers Containing p-Phenyl Propargyl Ether: Polymerization of Monomers and Properties of Polybenzoxazines

Macromolecules, 2001-10, Vol.34 (21), p.7257-7263

2001

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Influence of SEBS-g-MA on morphology, mechanical, and thermal properties of PA6/PP/organoclay nanocomposites

European polymer journal, 2008-04, Vol.44 (4), p.1023-1039

2008

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A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease

British journal of dermatology (1951), 2020-02, Vol.182 (2), p.491-493

2020

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Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study

Journal of the European Academy of Dermatology and Venereology, 2021-08, Vol.35 (8), p.e528-e531

2021

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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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Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation

British journal of dermatology (1951), 2017-10, Vol.177 (4), p.e133-e135

2017

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A juvenile male case of dermatofibrosarcoma protuberans on the breast

Clinical and experimental dermatology, 2020-01, Vol.45 (1), p.111-113

2020

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Cutaneous extramedullary hematopoiesis in a patient with secondary myelofibrosis due to MPL gene mutation

Journal of the European Academy of Dermatology and Venereology, 2021-04, Vol.35 (4), p.e257-e259

2021

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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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Polybenzoxazine–montmorillonite hybrid nanocomposites: synthesis and characterization

Polymer (Guilford), 2000, Vol.41 (19), p.7083-7090

2000

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Unique reticular hyperkeratotic eruptions seen in a patient with Darier's disease and attention deficit hyperactivity disorder

Journal of the European Academy of Dermatology and Venereology, 2020-01, Vol.34 (1), p.e41-e43

2020

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Two cases of generalized pustular psoriasis complicated by IgG4‐related disease

British journal of dermatology (1951), 2018-08, Vol.179 (2), p.537-539

2018

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A patient with bullous pemphigoid with mucosal involvement serologically positive for anti‐BP230 autoantibodies only

British journal of dermatology (1951), 2020-01, Vol.182 (1), p.221-223, Article bjd.18343

2020

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Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory

British journal of dermatology (1951), 2015-01, Vol.172 (1), p.94-100

2015

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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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Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C‐terminus of KIT

British journal of dermatology (1951), 2018-11, Vol.179 (5), p.1210-1211

2018

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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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Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RN

British journal of dermatology (1951), 2017-12, Vol.177 (6), p.1732-1736

2017

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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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A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient

British journal of dermatology (1951), 2018-02, Vol.178 (2), p.e111-e113

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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Mutational analysis of 29 patients with autosomal‐recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal‐recessive woolly hair and hypotrichosis in Japan

British journal of dermatology (1951), 2017-07, Vol.177 (1), p.290-292

2017

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Roles of aberrant hemichannel activities due to mutant connexin26 in the pathogenesis of KID syndrome

Studies on thermal and mechanical properties of polyimide–clay nanocomposites

Epithelioid cell granuloma formation in CARD14‐associated papulosquamous eruptions

Novel Benzoxazine Monomers Containing p-Phenyl Propargyl Ether: Polymerization of Monomers and Properties of Polybenzoxazines

Influence of SEBS-g-MA on morphology, mechanical, and thermal properties of PA6/PP/organoclay nanocomposites

A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease

Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study

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

Autosomal dominant familial generalized pustular psoriasis caused by a CARD14 mutation

A juvenile male case of dermatofibrosarcoma protuberans on the breast

Cutaneous extramedullary hematopoiesis in a patient with secondary myelofibrosis due to MPL gene mutation

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

Polybenzoxazine–montmorillonite hybrid nanocomposites: synthesis and characterization

Unique reticular hyperkeratotic eruptions seen in a patient with Darier's disease and attention deficit hyperactivity disorder

Two cases of generalized pustular psoriasis complicated by IgG4‐related disease

A patient with bullous pemphigoid with mucosal involvement serologically positive for anti‐BP230 autoantibodies only

Whole-exome sequencing improves mutation detection in a diagnostic epidermolysis bullosa laboratory

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

Autosomal dominant progressive hyperpigmentation and lentigines in a Japanese pedigree due to a missense mutation near the C‐terminus of KIT

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

Granulocyte and monocyte apheresis can control juvenile generalized pustular psoriasis with mutation of IL36RN

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

A novel IFIH1 mutation in the pincer domain underlies the clinical features of both Aicardi–Goutières and Singleton–Merten syndromes in a single patient

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

Mutational analysis of 29 patients with autosomal‐recessive woolly hair and hypotrichosis: LIPH mutations are extremely predominant in autosomal‐recessive woolly hair and hypotrichosis in Japan

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