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The Thermal Influence of an Electromagnetic Field with a Radio Frequency Depending on the Type of Electrode Used

International journal of environmental research and public health, 2022-09, Vol.19 (18), p.11378

2022

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SARS-CoV-2-induced disruption of a vascular bed in a microphysiological system caused by type-I interferon from bronchial organoids

Lab on a chip, 2024-01

2024

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Prevalence of filaggrin gene mutations in patients with atopic dermatitis and ichthyosis vulgaris in Kyushu area of Japan and South Korea

Journal of dermatological science, 2017-05, Vol.86 (2), p.174-177

2017

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Isolation of All CD44 Transcripts in Human Epidermis and Regulation of Their Expression by Various Agents

PloS one, 2016-08, Vol.11 (8), p.e0160952-e0160952

2016

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Evaluation of apoptosis-associated protein (Bcl-2, Bax, cleaved caspase-3 and p53) expression in canine mammary tumors: An immunohistochemical and prognostic study

Research in veterinary science, 2016-04, Vol.105, p.124-133

2016

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Elucidation of the liver pathophysiology of COVID-19 patients using liver-on-a-chips

PNAS nexus, 2023-03, Vol.2 (3), p.pgad029

2023

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A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome

Experimental dermatology, 2016-07, Vol.25 (7), p.568-570

2016

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Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease

Journal of dermatological science, 2014-07, Vol.75 (1), p.36-42

2014

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Ten cases of severe oral lichen planus showing granular C3 deposition in oral mucosal basement membrane zone

EJD. European journal of dermatology, 2015-11, Vol.25 (6), p.539-547

2015

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Isolation of all CD44 transcripts in human epidermis and regulation of their expression by various agents

Journal of dermatological science, 2016-10, Vol.84 (1), p.e40-e41

2016

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Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

Journal of dermatological science, 2015-04, Vol.78 (1), p.82-85

2015

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A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases

Journal of dermatological science, 2016-05, Vol.82 (2), p.134-137

2016

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Identification of CD44 transcripts that segregate with proliferation, redox and differentiation activities in human epidermal keratinocytes

Journal of dermatological science, 2016-10, Vol.84 (1), p.e110-e110

2016

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Towards understanding mechanisms of autoimmune bullous skin diseases

North American journal of medical sciences, 2013-10, Vol.5 (10), p.609-610

2013

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Mutation and pathogenic study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

Journal of dermatological science, 2016-10, Vol.84 (1), p.e48-e48

2016

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Corrigendum to ‘Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia’ [Journal of Dermatological Science 78 (2015) 82–85]

Journal of dermatological science, 2015-08, Vol.79 (2), p.179-180

2015

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2D LC as a tool for standardization of Foenugraeci semen extracts containing compounds with anti-Helicobacter pylori activity

Food & function, 2021-03, Vol.12 (6), p.2686-2692

2021

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New Frontiers in Electrocardiography, Cardiac Arrhythmias, and Arrhythmogenic Disorders

Journal of clinical medicine, 2024-04, Vol.13 (7), p.2047

2024

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Immunological and Statistical Studies of Anti-BP180 Antibodies in Paraneoplastic Pemphigus

Journal of investigative dermatology, 2014-08, Vol.134 (8), p.2283-2287

2014

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Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome

Pediatric research, 2007-04, Vol.61 (4), p.502-505

2007

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The impact of the distribution method for struvite (Crystal Green) on the chemical composition of soybean and their utility in animal nutrition

Scientific reports, 2024-01, Vol.14 (1), p.1093-1093, Article 1093

2024

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Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners

Experimental dermatology, 2014-09, Vol.23 (9), p.682-684

2014

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Could incarceration of inguinal hernia in children be prevented?

Medical science monitor, 2003-01, Vol.9 (1), p.CR16-CR18

2003

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Influence of different dispersants on the quality and stability of aqueous quinacridone magenta pigment dispersion for ink‐jet applications

Coloration technology, 2023-12, Vol.139 (6), p.637-653

2023

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Anti-early endosome antigen 1 autoantibodies were detected in a pemphigus-like patient but not in the majority of pemphigus diseases

Experimental dermatology, 2016-05, Vol.25 (5), p.368-374

2016

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The Thermal Influence of an Electromagnetic Field with a Radio Frequency Depending on the Type of Electrode Used

SARS-CoV-2-induced disruption of a vascular bed in a microphysiological system caused by type-I interferon from bronchial organoids

Prevalence of filaggrin gene mutations in patients with atopic dermatitis and ichthyosis vulgaris in Kyushu area of Japan and South Korea

Isolation of All CD44 Transcripts in Human Epidermis and Regulation of Their Expression by Various Agents

Evaluation of apoptosis-associated protein (Bcl-2, Bax, cleaved caspase-3 and p53) expression in canine mammary tumors: An immunohistochemical and prognostic study

Elucidation of the liver pathophysiology of COVID-19 patients using liver-on-a-chips

A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome

Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease

Ten cases of severe oral lichen planus showing granular C3 deposition in oral mucosal basement membrane zone

Isolation of all CD44 transcripts in human epidermis and regulation of their expression by various agents

Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases

Identification of CD44 transcripts that segregate with proliferation, redox and differentiation activities in human epidermal keratinocytes

Towards understanding mechanisms of autoimmune bullous skin diseases

Mutation and pathogenic study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia

Corrigendum to ‘Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia’ [Journal of Dermatological Science 78 (2015) 82–85]

2D LC as a tool for standardization of Foenugraeci semen extracts containing compounds with anti-Helicobacter pylori activity

New Frontiers in Electrocardiography, Cardiac Arrhythmias, and Arrhythmogenic Disorders

Immunological and Statistical Studies of Anti-BP180 Antibodies in Paraneoplastic Pemphigus

Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome

The impact of the distribution method for struvite (Crystal Green) on the chemical composition of soybean and their utility in animal nutrition

Human dermal fibroblast migration induced by fibronectin in autocrine and paracrine manners

Could incarceration of inguinal hernia in children be prevented?

Influence of different dispersants on the quality and stability of aqueous quinacridone magenta pigment dispersion for ink‐jet applications

Anti-early endosome antigen 1 autoantibodies were detected in a pemphigus-like patient but not in the majority of pemphigus diseases

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