H. Niizeki

发表

A novel indel COL7A1 mutation 8068del17insGA causes dominant dystrophic epidermolysis bullosa

H. Shimizu, S. Miyagawa, D. Sawamura, 2006, The British journal of dermatology.

Novel homozygous mutation, c.400C>T (p.Arg134*), in the PVRL1 gene underlies cleft lip/palate‐ectodermal dysplasia syndrome in an Asian patient

M. Kubota, Kazue Yoshida, Y. Shimomura, 2015, The Journal of dermatology.

HLA-DQA1, -DQB1 and -DRB1 genotyping in Japanese pemphigus vulgaris patients by the PCR-RFLP method.

H. Inoko, T. Nishikawa, H. Niizeki, 1994, Tissue antigens.

Novel heterozygous mutation, c.74C>G (p.Pro25Arg), in the U2HR gene underlies Marie Unna hereditary hypotrichosis in a Japanese family

Kazue Yoshida, Y. Shimomura, H. Niizeki, 2017, The Journal of dermatology.

Transepidermal water loss measurement during infancy can predict the subsequent development of atopic dermatitis regardless of filaggrin mutations.

Takashi Sasaki, E. Inoue, Y. Ohya, 2016, Allergology international : official journal of the Japanese Society of Allergology.

Application of moisturizer to neonates prevents development of atopic dermatitis.

Takashi Sasaki, E. Inoue, Y. Ohya, 2014, The Journal of allergy and clinical immunology.

Lack of association of the interleukin-1 receptor antagonist gene with palmoplantar pustulosis in Japanese.

H. Inoko, T. Nishikawa, T. Naruse, 2003, European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics.

Complete type of pachydermoperiostosis with a novel mutation c.510G>A of the SLCO2A1 gene

K. Nakabayashi, Y. Tokura, H. Niizeki, 2017, The Journal of dermatology.

Genotyping for HLA‐A, B and C alleles in Japanese patients with pemphigus: prevalence of Asian alleles of the HLA‐B15 family

Y. Yamashina, S. Miyagawa, H. Niizeki, 2002, The British journal of dermatology.

Prenatal diagnosis of oculocutaneous albinism by analysis of the fetal tyrosinase gene.

H. Shimizu, T. Nishikawa, R. Kawaguchi, 1994, The Journal of investigative dermatology.

Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations.

T. Kanekura, Y. Chinen, Tamio Suzuki, 2016, Journal of dermatological science.

Polymorphism in the tumor necrosis factor B gene is associated with Palmoplantar pustulosis.

H. Shimizu, T. Nishikawa, K. Hashigucci, 1999, Tissue antigens.

A new concept of skin-associated lymphoid tissue (SALT): UVB light impaired cutaneous immunity reveals a prominent role for cutaneous nerves.

J. Streilein, H. Niizeki, P. Alard, 1999, The Keio journal of medicine.

Adjuvant effect of lipopolysaccharide on the induction of contact hypersensitivity to haptens in mice.

H. Asada, S. Miyagawa, H. Niizeki, 2009, Journal of dermatological science.

Polymorphisms in the tumor necrosis factor (TNF) genes are associated with susceptibility to effects of ultraviolet-B radiation on induction of contact hypersensitivity.

H. Inoko, T. Naruse, J. Taylor, 2001, Tissue antigens.

A case of pemphigus foliaceus after interferon alpha-2a therapy.

T. Nishikawa, K. Nakamura, H. Niizeki, 1994, Dermatology.

Neural Influences on Induction of Contact Hypersensitivity

J. Streilein, H. Niizeki, P. Alard, 1999, Annals of the New York Academy of Sciences.

Inhibition of programmed cell death by cyclosporin A; preferential blocking of cell death induced by signals via TCR/CD3 complex and its mode of action.

T. Tadakuma, H. Kizaki, H. Niizeki, 1992, Immunology.

Hapten‐specific tolerance induced by acute, low‐dose ultraviolet B radiation of skin requires mast cell degranulation

J. Streilein, H. Niizeki, P. Alard, 2001, European journal of immunology.

A substance p agonist acts as an adjuvant to promote hapten-specific skin immunity.

J. Streilein, H. Niizeki, I. Kurimoto, 1998, The Journal of investigative dermatology.

Regulatory effects of antihistamines on the responses to staphylococcal enterotoxin B of human monocyte-derived dendritic cells and CD4+ T cells.

H. Asada, E. Kita, S. Miyagawa, 2008, Journal of dermatological science.

Role for connexin 26 in metastasis of human malignant melanoma

H. Asada, H. Nojima, H. Kuniyasu, 2007, Cancer.

XXIV World Allergy Congress 2015

Dong Hun Lee, Young Han Kim, Byung Soo Kim, 2016, The World Allergy Organization Journal.

Polymorphisms in the TNFA promoter region is not associated with palmoplantar pustulosis.

H. Inoko, T. Nishikawa, T. Naruse, 2000, Tissue antigens.

Intravascular histiocytosis associated with rheumatoid arthritis: report of a case with lymphatic endothelial proliferation

A. Nonomura, S. Miyagawa, H. Niizeki, 2005, The British journal of dermatology.

A clinical feature associated with polymorphisms of the TNF region in Japanese patients with palmoplantar pustulosis.

H. Inoko, T. Nishikawa, M. Ota, 2003, Human immunology.

Exclusion of the TAP1 and TAP2 genes within the HLA class II region as candidate susceptibility genes to pemphigus in the Japanese population.

T. Nishikawa, M. Amagai, Y. Yamashina, 2004, Journal of dermatological science.

Distinct Characteristics in Japanese Dermatitis Herpetiformis: A Review of All 91 Japanese Patients over the Last 35 Years

T. Dainichi, T. Hashimoto, Y. Shimomura, 2012, Clinical & developmental immunology.

HLA-DRB1 polymorphisms and autoimmune responses to desmogleins in Japanese patients with pemphigus.

H. Inoko, T. Nishikawa, M. Amagai, 1999, Tissue antigens.

Unusually located lymphocutaneous nocardiosis caused by Nocardia brasiliensis

T. Nishikawa, Y. Mikami, H. Niizeki, 1995, The British journal of dermatology.

Paraneoplastic pemphigus presenting as erythrodermic lichenoid dermatitis with concomitant features of pemphigus foliaceus

H. Asada, T. Hashimoto, N. Kobayashi, 2007, The Journal of dermatology.

Japanese guidelines for the management of pemphigus

M. Amagai, T. Hashimoto, Y. Aoyama, 2014, The Journal of dermatology.

Polymorphisms in the TNF region confer susceptibility to UVB-induced impairment of contact hypersensitivity induction in mice and humans.

H. Inoko, H. Niizeki, J. Wayne Streilein, 2002, Methods.

Local ultraviolet B irradiation impairs contact hypersensitivity induction by triggering release of tumor necrosis factor-alpha from mast cells. Involvement of mast cells and Langerhans cells in susceptibility to ultraviolet B.

J. Streilein, H. Niizeki, P. Alard, 1999, The Journal of investigative dermatology.

Effectiveness of non-steroidal anti-inflammatory drugs among patients with primary hypertrophic osteoarthropathy: A systematic review.

E. Ota, P. Shakya, L. Mlunde, 2017, Journal of dermatological science.

Pathological characterization of pachydermia in pachydermoperiostosis

A. Shiohama, Takashi Sasaki, J. Kudoh, 2015, The Journal of dermatology.

Calcitonin gene-related peptide is necessary for ultraviolet B-impaired induction of contact hypersensitivity.

J. Streilein, H. Niizeki, P. Alard, 1997, Journal of immunology.

An epidemiological survey of anhidrotic/hypohidrotic ectodermal dysplasia in Japan: High prevalence of allergic diseases

Kazue Yoshida, Y. Shimomura, H. Yokozeki, 2021, The Journal of dermatology.

Grading criteria for disease severity by pemphigus disease area index

T. Takebayashi, V. Werth, M. Amagai, 2014, The Journal of dermatology.

Contact dermatitis from ketotifen fumarate eyedrops

H. Niizeki, N. Inamoto, J. Nakanoma, 1994, Contact dermatitis.

Compound heterozygous mutations including a de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity.

J. R. McMillan, M. Akiyama, H. Shimizu, 2006, The Journal of investigative dermatology.

Ampicillin-induced cutaneous eruption associated with Epstein-Barr virus reactivation.

H. Asada, S. Miyagawa, H. Niizeki, 2005, Journal of the American Academy of Dermatology.

Unique characteristics in Japanese dermatitis herpetiformis

H. Inoko, J. Zone, Y. Shimomura, 2016, British Journal of Dermatology.

HLA class II antigens are associated with Japanese pemphigus patients.

A Ando, H. Inoko, T. Tadakuma, 1991, Human immunology.

Delayed‐onset heat intolerance in a Japanese patient with X‐linked hypohidrotic ectodermal dysplasia associated with a large deletion involving four genes

R. Abe, Kazue Yoshida, Y. Shimomura, 2018, The Journal of dermatology.

Novel EDA hemizygous frame‐shift mutation c. 731delG (p.R244Qfs*36) underlies hypohidrotic ectodermal dysplasia in a Japanese family

Kazue Yoshida, Y. Shimomura, H. Niizeki, 2014, The Journal of dermatology.

A Japanese case of the fibrillar type of dermatitis herpetiformis.

H. Shimizu, T. Nishikawa, T. Hashimoto, 1995, Dermatology.

Relationship among human herpesvirus 6 reactivation, serum interleukin 10 levels, and rash/graft-versus-host disease after allogeneic stem cell transplantation.

H. Asada, N. Kobayashi, S. Miyagawa, 2008, Journal of the American Academy of Dermatology.

Mutations in SERPINB7, encoding a member of the serine protease inhibitor superfamily, cause Nagashima-type palmoplantar keratosis.

A. Shiohama, Takashi Sasaki, J. Kudoh, 2013, American Journal of Human Genetics.

Mosquito salivary gland extracts induce EBV-infected NK cell oncogenesis via CD4 T cells in patients with hypersensitivity to mosquito bites.

H. Asada, S. Miyagawa, Y. Tokura, 2005, The Journal of investigative dermatology.

Safety and Efficacy of the Sirolimus Gel for TSC Patients With Facial Skin Lesions in a Long-Term, Open-Label, Extension, Uncontrolled Clinical Trial

H. Nagai, M. Wataya-Kaneda, H. Yokozeki, 2020, Dermatology and Therapy.

Sirolimus Gel Treatment vs Placebo for Facial Angiofibromas in Patients With Tuberous Sclerosis Complex: A Randomized Clinical Trial

H. Nagai, M. Wataya-Kaneda, H. Yokozeki, 2018, JAMA dermatology.

Bucillamine‐Induced Toxic Epidermal Necrolysis and Fixed Drug Eruption

H. Asada, N. Kobayashi, S. Katsumi, 2005, The Journal of dermatology.

Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype-genotype correlation in Japanese patients with pachydermoperiostosis.

H. Okano, A. Shiohama, Takashi Sasaki, 2012, Journal of dermatological science.

Hapten-specific tolerance induced by acute, low-dose ultraviolet B radiation of skin is mediated via interleukin-10.

J. Streilein, H. Niizeki, 1997, The Journal of investigative dermatology.

A male Korean who was diagnosed with chronic enteropathy associated with SLCO2A1 (CEAS): case report with literature review

H. Ogata, N. Hosoe, T. Kanai, 2018, BMJ open gastroenterology.

[HLA antigens in 11 cases of patients with recurrent erythema and anti-SS-B antibody].

T. Nishikawa, T. Hashimoto, H. Niizeki, 1990, Nihon Hifuka Gakkai zasshi. The Japanese journal of dermatology.

Role of Prostaglandin E-major Urinary Metabolite Levels in Identifying the Phenotype of Pachydermoperiostosis.

T. Nomura, K. Kabashima, H. Niizeki, 2021, Journal of Investigative Dermatology.

Infiltration of mast cells in pachydermia of pachydermoperiostosis

K. Nakabayashi, Y. Tokura, K. Tanese, 2017, The Journal of dermatology.

The novel SLCO2A1 heterozygous missense mutation p.E427K and nonsense mutation p.R603* in a female patient with pachydermoperiostosis with an atypical phenotype

A. Shiohama, J. Kudoh, K. Kabashima, 2014, The British journal of dermatology.

Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations

H. Mizukami, K. Kabashima, K. Nakabayashi, 2015, The Journal of dermatology.

Involvement of prostaglandin E2 in the first Japanese case of pachydermoperiostosis with HPGD mutation and recalcitrant leg ulcer.

K. Nakabayashi, Y. Tokura, H. Niizeki, 2015, Journal of dermatological science (Amsterdam).

The complete type of pachydermoperiostosis: a novel nonsense mutation p.E141* of the SLCO2A1 gene.

A. Shiohama, J. Kudoh, K. Matsuoka, 2014, Journal of dermatological science.

Eicosanoid profiling in patients with complete form of pachydermoperiostosis carrying SLCO2A1 mutations

T. Nomura, R. Uozumi, K. Kabashima, 2021, The Journal of dermatology.

Congenital nail clubbing

K. Nakabayashi, Y. Tokura, K. Tanese, 2018, The Journal of dermatology.

Primary hypertrophic osteoarthropathy with severe arthralgia identified by gene mutation of SLCO2A1

H. Morita, K. Nakabayashi, H. Niizeki, 2020, Modern rheumatology case reports.

First Japanese case of congenital generalized hypertrichosis with a copy number variation on chromosome 17q24.

R. Abe, Y. Shimomura, H. Niizeki, 2017, Journal of dermatological science.

Linear keratinocytic epidermal nevi on trunk skin caused by a somatic FGFR2 p.C382R mutation

Takashi Sasaki, N. Umegaki-Arao, A. Kubo, 2018, The Journal of dermatology.

Intestinal Behçet disease: serial changes at radiography.

M. Fujishima, T. Matsumoto, M. Iida, 1993, Radiology.

Japanese guidelines for the management of pemphigus

M. Amagai, T. Hashimoto, Y. Aoyama, 2014, The Journal of dermatology.

Distinct roles for transforming growth factor-beta2 and tumour necrosis factor-alpha in immune deviation elicited by hapten-derivatized antigen-presenting cells.

K. Hecker, J. Streilein, H. Niizeki, 1999, Immunology.

Occult myopathy of the vastus intermedius muscles detected by magnetic resonance imaging in subclinical dermatomyositis: report of two cases

S. Kuramochi, H. Niizeki, M. Nishikai, 2003, Modern Rheumatology.

Unique characteristics in Japanese dermatitis herpetiformis

H. Inoko, J. Zone, H. Uhara, 2016, British Journal of Dermatology.

The MICA5.1 allele is not associated with susceptibility to effects of ultraviolet-B radiation on induction of contact hypersensitivity.

H. Inoko, T. Naruse, T. Iwata, 2004, Journal of dermatological science.

Splicing abnormality of integrin β4 gene (ITGB4) due to nucleotide substitutions far from splice site underlies pyloric atresia-junctional epidermolysis bullosa syndrome.

M. Amagai, T. Masunaga, H. Niizeki, 2015, Journal of dermatological science.

Genetic analyses of oculocutaneous albinism types 2 and 4 with eight novel mutations.

T. Kanekura, Y. Chinen, Tamio Suzuki, 2016, Journal of dermatological science.