Y. Tomita

发表

Dyschromatosis symmetrica hereditaria associated with neurological disorders

T. Negoro, Tamio Suzuki, M. Kono, 2008, The Journal of dermatology.

Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria: Histological observation and comparison of genotypes and clinical phenotypes

M. Komine, H. Akita, Tamio Suzuki, 2008, The Journal of dermatology.

Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis.

H. Shimizu, Kunihiro Yoshida, T. Horikawa, 2005, The Journal of investigative dermatology.

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria.

Tamio Suzuki, M. Kono, Y. Miyamura, 2003, American journal of human genetics.

Overexpression of LEDGF/DFS70 induces IL-6 via p38 activation in HaCaT cells, similar to that seen in the psoriatic condition.

O. Kaminuma, Y. Shimoyama, Kenji Matsumoto, 2010, The Journal of investigative dermatology.

Epidermal growth factor receptor tyrosine kinase inhibitors induce CCL2 and CCL5 via reduction in IL‐1R2 in keratinocytes

Y. Shimoyama, Y. Muro, K. Sugiura, 2010, Experimental dermatology.

Postoperative DAV‐IFN‐β therapy does not improve survival rates of stage II and stage III melanoma patients significantly

H. Yatsuya, M. Akiyama, K. Yokota, 2013, Journal of the European Academy of Dermatology and Venereology.

Interval sentinel lymph nodes in patients with cutaneous melanoma: A single‐institution study in Japan

K. Yokota, Y. Shimoyama, Katsuhiko Kato, 2010, The Journal of dermatology.

Molecular cloning of cDNA encoding a novel microphthalmia-associated transcription factor isoform with a distinct amino-terminus.

K. Takahashi, S. Shibahara, M. Tamai, 1999, Journal of biochemistry.

Autoantibodies to DFS70/LEDGF are increased in alopecia areata patients.

Y. Shimomura, Y. Muro, T. Nagasaka, 2004, Journal of autoimmunity.

HLA-associated production of anti-DFS70/LEDGF autoantibodies and systemic autoimmune disease.

Y. Muro, Y. Ogawa, K. Sugiura, 2006, Journal of autoimmunity.

Anti-p80 coilin autoantibodies react with a conserved epitope and are associated with anti-DFS70/LEDGF autoantibodies.

Y. Muro, Y. Ogawa, K. Sugiura, 2006, Journal of autoimmunity.

LEDGF/DFS70, a major autoantigen of atopic dermatitis, is a component of keratohyalin granules.

T. Shinohara, J. Usukura, Y. Muro, 2008, The Journal of investigative dermatology.

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

Y. Muro, K. Sugiura, Y. Tomita, 2008, Lupus.

IgE and IgG4 autoantibodies against DFS70/LEDGF in atopic dermatitis

Y. Muro, K. Sugiura, Kanako Watanabe, 2011, Autoimmunity.

The unfolded protein response is activated in differentiating epidermal keratinocytes.

Kenji Matsumoto, J. Usukura, H. Saito, 2009, The Journal of investigative dermatology.

Identification of a cis-acting element that enhances the pigment cell-specific expression of the human tyrosinase gene.

S. Shibahara, H. Tagami, H. Tagami, 1992, The Journal of biological chemistry.

Anti-MDA5 and anti-TIF1-gamma antibodies have clinical significance for patients with dermatomyositis.

T. Mimori, Y. Muro, K. Sugiura, 2010, Rheumatology.

Anti-MDA 5 and anti-TIF 1-c antibodies have clinical significance for patients with dermatomyositis

T. Mimori, Y. Muro, K. Sugiura, 2010 .

Anti-SSA / Ro antibody determination by indirect immunofluorescence and comparison of different methods of anti-nuclear antibody screening Evaluation of the utility of HEp-2 cells transfected with the 60 kDa SSA / Ro as a substrate

Y. Muro, K. Sugiura, Y. Tomita, 2008 .

Anti-SS-A/Ro antibody determination by indirect immunofluorescence and comparison of different methods of anti-nuclear antibody screening

Y. Muro, K. Sugiura, Y. Tomita, 2008, Modern rheumatology.

Anti-SS-A/Ro antibody determination by indirect immunofluorescence and comparison of different methods of anti-nuclear antibody screening

Y. Muro, K. Sugiura, Y. Tomita, 2008 .

Malignant melanoma of mucous membranes. A clinicopathologic study of 13 cases in Japanese patients.

R. Abe, M. Takahashi, Y. Tomita, 1987, Archives of dermatology.

A pilot study of human interferon beta gene therapy for patients with advanced melanoma by in vivo transduction using cationic liposomes.

T. Saida, M. Mizuno, J. Yoshida, 2008, Japanese Journal of Clinical Oncology.

Anti-cyclic citrullinated peptide antibody in systemic sclerosis.

Y. Muro, K. Sugiura, Y. Tomita, 2008, Clinical and experimental rheumatology.

Differences in specificities of anti-centromere sera for the monomeric and dimeric C-terminal peptides of human centoromere protein C.

K. Sugimoto, Y. Muro, Y. Tomita, 2000, International immunology.

Detection of various types of human papillomavirus DNA, mainly belonging to the cutaneous-group, more frequently in normal tissue than in squamous cell carcinomas of the lip.

H. Tagami, Y. Kusakari, T. Nagasaka, 2004, Journal of dermatological science.

Effects of single therapeutic doses of promethazine, fexofenadine and olopatadine on psychomotor function and histamine-induced wheal- and flare-responses: a randomized double-blind, placebo-controlled study in healthy volunteers

T. Nabeshima, Kiyofumi Yamada, Y. Noda, 2011, Archives of Dermatological Research.

Molecular cloning and functional analysis of a cDNA coding for human DOPAchrome tautomerase/tyrosinase-related protein-2.

H. Suzuki, S. Shibahara, K. Yasumoto, 1994, Biochimica et biophysica acta.

MAT-1, a monoclonal antibody that specifically recognizes human tyrosinase.

S. Shibahara, Y. Tomita, S. Suzuki, 1995, The Journal of investigative dermatology.

An evaluation of the efficacy of the toe brachial index measuring vascular involvement in systemic sclerosis and other connective tissue diseases.

Y. Muro, K. Sugiura, Y. Tomita, 2009, Clinical and experimental rheumatology.

Cyclosporin A induces the unfolded protein response in keratinocytes

Y. Shimoyama, Y. Muro, K. Sugiura, 2011, Archives of Dermatological Research.

Radical production during tyrosinase reaction, dopa-melanin formation, and photoirradiation of dopa-melanin.

M. Seiji, Y. Tomita, Yasushi Tomita, 1984, The Journal of investigative dermatology.

Identification of mutations in the pigment cell-specific gene located at the brown locus in mouse.

S. Shibahara, H. Tagami, Y. Tomita, 2008, Pigment cell research.

Dermoscopic evaluation of vascular structures of various skin tumors in Japanese patients

M. Kamijima, M. Kono, Y. Tomita, 2010, The Journal of dermatology.

Characterization of the human RAB38 and RAB7 genes: exclusion of new major pathological loci for Japanese OCA.

Tamio Suzuki, Y. Miyamura, Y. Tomita, 2003, Journal of dermatological science.

Cloning and expression of cDNA encoding mouse tyrosinase.

S. Shibahara, R. Müller, B. Chaudhuri, 1986, Nucleic acids research.

Nucleotide sequence of the cDNA encoding human tyrosinase-related protein.

S. Shibahara, Y. Tomita, T. Cohen, 1990, Nucleic acids research.

Human oculocutaneous albinism caused by single base insertion in the tyrosinase gene.

A. Takeda, S. Shibahara, H. Tagami, 1989, Biochemical and biophysical research communications.

Cross-reactivity of murine monoclonal anti-DNA antibodies with human and murine skin: a possible pathogenetic role in skin lesions of lupus erythematosus.

H. Tagami, S. Aiba, Y. Tomita, 1989, The Journal of investigative dermatology.

Stimulation of melanogenesis by cholecalciferol in cultured human melanocytes: a possible mechanism underlying pigmentation after ultraviolet irradiation.

H. Tagami, Y. Tomita, M. Fukushima, 1986, The Tohoku journal of experimental medicine.

Establishment of a screening system for chemicals that upregulate a melanoma antigen, Melan-A/MART-1.

M. Kono, Y. Tomita, H. Song, 2009, The Tohoku journal of experimental medicine.

Improvement of Systemic Sclerosis Complicated with Interstitial Lung Disease by Intravenous Pulse Therapy with Cyclophosphamide

Y. Muro, Y. Tomita, J. Kuroda, 2006 .

Clinical features and IgG subclass distribution of anti-p80 coilin antibodies.

Y. Muro, Y. Tomita, H. Onouchi, 1999, Journal of autoimmunity.

Human papillomaviruses of the mucosal type are present in some cases of extragenital Bowen's disease

T. Nagasaka, Y. Tomita, A. Sakakibara, 2005, The British journal of dermatology.

Sequence-Based Diagnosis of Tyrosinase-Related Oculocutaneous Albinism: Successful Sequence Analysis of the Tyrosinase Gene from Blood Spots Dried on Filter Paper

Y. Miyamura, Y. Tomita, K. Satomura, 1998, Dermatology.

Sequence analysis of the human tyrosinase promoter from a patient with tyrosinase-negative oculocutaneous albinism.

Y. Miyamura, Y. Tomita, J. Matsunaga, 1997, Pigment cell research.

R278TER and P431L mutations of the tyrosinase gene exist in Japanese patients with tyrosinase-negative oculocutaneous albinism.

H. Shimizu, Y. Tomita, J. Matsunaga, 1996, Journal of dermatological science.

Stimulation of human melanocytes by vitamin D3 possibly mediates skin pigmentation after sun exposure.

H. Tagami, H. Tagami, Y. Tomita, 1988, The Journal of investigative dermatology.

XPA gene mutations resulting in subtle truncation of protein in xeroderma pigmentosum group A patients with mild skin symptoms.

S. Moriwaki, M. Iijima, M. Takigawa, 2010, The Journal of investigative dermatology.

Primary cutaneous CD30 positive T‐cell lymphoproliferative disorders with aberrant expression of PAX5: Report of three cases

K. Takata, T. Yoshino, A. Tomita, 2012, Pathology international.

Primary cutaneous T‐cell lymphoma of unspecified type with cytotoxic phenotype: Clinicopathological analysis of 27 patients

K. Takata, T. Yoshino, Y. Tamada, 2009, Cancer science.

Limited Cutaneous Systemic Sclerosis with Rapid Progression of Edematous Stiffness on the Forearms

Y. Muro, Y. Tomita, Mayumi Hirota, 2006 .

Spectrum of autoantibodies against a dynamin-related protein, dymple.

M. Hagiwara, T. Kamimoto, Y. Muro, 2000, Arthritis and rheumatism.

Comparison of the melanogenesis in human black and light brown melanocytes.

Y. Yokokawa, Y. Tomita, K. Maeda, 1997, Journal of dermatological science.

Monoclonal antibody MAT-1 against human tyrosinase can detect melanogenic cells on formalin-fixed paraffin-embedded sections.

Y. Tomita, S. Suzuki, H. Takimoto, 1996, Pigment cell research.

Histamine stimulates normal human melanocytes in vitro: one of the possible inducers of hyperpigmentation in urticaria pigmentosa.

H. Tagami, Y. Tomita, K. Maeda, 1993, Journal of dermatological science.

Microsatellite-based genotyping of Candida albicans isolated from patients with superficial candidiasis.

M. Akiyama, T. Kanbe, R. Tanaka, 2011, Medical mycology journal.

A case of a childhood linear scleroderma with limb asymmetry

Y. Muro, K. Sugiura, Y. Tomita, 2004, Modern rheumatology.

The effect of the long-term cultivation on telomere length and morphology of cultured epidermis.

H. Kagami, A. Fujimoto, M. Ueda, 2004, Journal of dermatological science.

Detection of mouse tyrosinase with a monoclonal antibody MAT-1 against human tyrosinase.

S. Shibahara, Y. Tomita, S. Suzuki, 1996, Pigment cell research.

Anti‐Ribosomal‐P Antibodies in a Sjögren Syndrome Patient Associated with Lupus Erythematosus

Y. Muro, Y. Tomita, 2004, The Journal of dermatology.

GD3 synthase gene knockout mice exhibit thermal hyperalgesia and mechanical allodynia but decreased response to formalin-induced prolonged noxious stimulation

Kazuro Furukawa, K. Furukawa, K. Furukawa, 2005, Pain.

Molecular bases of tyrosinase-negative oculocutaneous albinism: a single base insertion or a missense point mutation in the tyrosinase gene.

S. Shibahara, H. Tagami, S. Okinaga, 2008, Pigment cell research.

Downstream region of the human tyrosinase-related protein gene enhances its promoter activity.

S. Shibahara, H. Tagami, Y. Tomita, 1992, Biochemical and biophysical research communications.

Functional analysis of the cDNA encoding human tyrosinase precursor.

S. Shibahara, H. Tagami, S. Okinaga, 1989, Biochemical and biophysical research communications.

Transfer of tyrosinase to melanosomes in Harding-Passey mouse melanoma.

M. Seiji, Y. Tomita, C. Kato, 1983, Archives of biochemistry and biophysics.

ELECTROPHORETIC PROFILE OF TYROSINASE TREATED WITH NEURAMINIDASE IN VARIOUS SUBCELLULAR FRACTIONS FROM MOUSE MELANOMA *

M. Seiji, Y. Tomita, Yasushi Tomita, 1979, The Journal of dermatology.

Specific distribution patterns of hCDC47 expression in cutaneous diseases

M. Fujita, A. Hiraiwa, M. Ohashi, 1998, Journal of cutaneous pathology.

Epithelioid sarcoma on the foot masquerading as an intractable wound for > 18 years

I. Katayama, A. Morita, Y. Yamaguchi, 2010, Clinical and experimental dermatology.

Ultrastructural features of trafficking defects are pronounced in melanocytic nevus in Hermansky-Pudlak syndrome type 1.

M. Akiyama, H. Shimizu, K. Natsuga, 2005, The Journal of investigative dermatology.

Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4.

Tamio Suzuki, Y. Tomita, 2008, Journal of dermatological science.

High frequency of the Ala481Thr mutation of the P gene in the Japanese population

Tamio Suzuki, Y. Miyamura, Y. Tomita, 2003, American journal of medical genetics. Part A.

OCA4: evidence for a founder effect for the p.D157N mutation of the MATP gene in Japanese and Korean.

Tamio Suzuki, S. Ito, Y. Tomita, 2005, Pigment cell research.

LEDGF/DFS70, a Major Autoantigen of Atopic Dermatitis, Is a Component of Keratohyalin Granules

T. Shinohara, J. Usukura, Y. Muro, 2007 .

Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene

S. Shibahara, K. Yasumoto, K. Yokoyama, 1995, Molecular and cellular biology.

Structural organization of the pigment cell-specific gene located at the brown locus in mouse. Its promoter activity and alternatively spliced transcript.

S. Shibahara, H. Tagami, Y. Tomita, 1991, The Journal of biological chemistry.

Mechanism of the Inhibitory Effect of Tranexamic Acid on Melanogenesis in Cultured Human Melanocytes in the Presence of Keratinocyte-conditioned Medium

Y. Tomita, K. Maeda, 2007 .

Melanocyte-stimulating properties of arachidonic acid metabolites: possible role in postinflammatory pigmentation.

H. Tagami, H. Tagami, Y. Tomita, 1992, Pigment cell research.

Leukotrienes and thromboxane B2 stimulate normal human melanocytes in vitro: possible inducers of postinflammatory pigmentation.

H. Tagami, Y. Tomita, K. Maeda, 1988, The Tohoku journal of experimental medicine.

Stimulatory effect of prostaglandin E2 on the configuration of normal human melanocytes in vitro.

H. Tagami, H. Tagami, M. Iwamoto, 1987, The Journal of investigative dermatology.

Results of the Health Assessment Questionnaire for Japanese patients with systemic sclerosis--measuring functional impairment in systemic sclerosis versus other connective tissue diseases.

K. Tamakoshi, Y. Muro, K. Sugiura, 2007, Clinical and experimental rheumatology.

The Successful Use of Topical Tacrolimus Treatment for a Chronic Actinic Dermatitis Patient with Complications of Idiopathic Leukopenia

Y. Ogawa, Y. Tomita, A. Adachi, 2003, The Journal of dermatology.

Contact sensitivity to Pityrosporum ovale in patients with atopic dermatitis.

H. Tagami, Y. Tomita, M. Rokugo, 1990, Archives of dermatology.

PCR and PCR-RFLP techniques targeting the DNA topoisomerase II gene for rapid clinical diagnosis of the etiologic agent of dermatophytosis.

T. Kanbe, A. Kikuchi, Y. Tomita, 2004, Journal of dermatological science.

Antigenic components of Malassezia species for immunoglobulin E antibodies in sera of patients with atopic dermatitis.

T. Kanbe, A. Kikuchi, Y. Tomita, 2001, Journal of dermatological science.

Isolation and Characterization of a Major Antigenic Component of Malassezia globosa to IgE Antibodies in Sera of Patients with Atopic Dermatitis

T. Kanbe, A. Kikuchi, Y. Tomita, 2000, Microbiology and immunology.

Histamine is involved in ultraviolet B-induced pigmentation of guinea pig skin.

Y. Tomita, Masaki Yoshida, H. Uchiwa, 2002, The Journal of investigative dermatology.

Stimulatory effect of histamine on normal human melanocytes in vitro.

H. Tagami, Y. Tomita, K. Maeda, 1988, The Tohoku journal of experimental medicine.

Two Cases of Subepidermal Blistering Disease with Anti-p200 or 180-kD Bullous Pemphigoid Antigen Associated with Psoriasis

T. Hashimoto, A. Shibaki, Y. Tomita, 2004, Dermatology.

Genotype analysis of Candida albicans isolates obtained from different body locations of patients with superficial candidiasis using PCRs targeting 25S rDNA and ALT repeat sequences of the RPS.

Yasushi Tomita, Toshio Kanbe, Fumihiko Kawamoto, 2006, Journal of dermatological science.

Effects of topical vehicles on growth of the lipophilic Malassezia species.

T. Kanbe, A. Kikuchi, Y. Tomita, 2002, Journal of dermatological science.

Detection of IgE Antibodies Specific for Malassezia Species in Sera of the Patients with Atopic Dermatitis

T. Kanbe, A. Kikuchi, Y. Tomita, 2000 .

Multiple Pigmented Basal Cell Carcinomas Arising in the Normal‐Appearing Skin After Radiotherapy for Carcinoma of the Cervix

Tamio Suzuki, Y. Tomita, Y. Handa, 2003, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

Genotyping of Candida albicans on the basis of polymorphisms of ALT repeats in the repetitive sequence (RPS).

T. Kanbe, A. Kikuchi, Y. Mikami, 2006, Journal of dermatological science.

Epidemiological study of Candida species in cutaneous candidiasis based on PCR using a primer mix specific for the DNA topoisomerase II gene.

T. Kanbe, A. Kikuchi, Y. Tomita, 2005, Journal of dermatological science.

Improvement in survival rate of patients with acral melanoma observed in the past 22 years in Sendai, Japan

H. Tagami, Y. Sugiyama, H Tagami, 1993, Clinical and experimental dermatology.

Genotyping of Candida albicans by fragment analysis of microsatellites combined with 25S rDNA and RPS-based strategies.

T. Kanbe, R. Tanaka, H. Chibana, 2009, Nihon Ishinkin Gakkai zasshi = Japanese journal of medical mycology.

Zeis Gland Carcinoma

Y. Tomita, N. Kato, A. Sotodate, 1997, The Journal of dermatology.

Extramammary Paget's Disease with Distant Skin Metastasis

K. Matsue, Y. Tomita, N. Kato, 1996, The Journal of dermatology.

The role of polymorphonuclear leukocyte infiltration in herpes simplex virus infection of murine skin

Y. Nishiyama, D. Watanabe, Y. Tomita, 1999, Archives of Dermatological Research.

Involvement of the tongue by lymphomatoid papulosis.

H. Hisai, Y. Tomita, K. Yoshida, 1998, The American Journal of dermatopathology.

Characteristic Intracytoplasmic Material in a Perianal Wart That Contains Human Papillomavirus Type 56 and 16 DNA

Tamio Suzuki, Y. Tomita, A. Adachi, 2001, Dermatology.

Large Ulcerated Perianal Hidradenoma Papilliferum in a Young Female

Y. Tomita, Y. Handa, 2003, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

Mammalian tyrosinase: biosynthesis, processing, and modulation by melanocyte-stimulating hormone.

V. Hearing, W. Maloy, Y. Tomita, 1988, Proceedings of the National Academy of Sciences of the United States of America.

The expression of tyrosinase, tyrosinase-related proteins 1 and 2 (TRP1 and TRP2), the silver protein, and a melanogenic inhibitor in human melanoma cells of differing melanogenic activities.

S. Kuge, K. Wakamatsu, V. Hearing, 1995, Pigment cell research.

Anti-T4-tyrosinase monoclonal antibodies--specific markers for pigmented melanocytes.

V. Hearing, P. Montague, Y. Tomita, 1985, The Journal of investigative dermatology.

Inactivation of tyrosinase by dopa.

M. Seiji, Y. Tomita, A. Hariu, 1980, The Journal of investigative dermatology.

INACTIVATION MECHANISM OF TYROSINASE IN MOUSE MELANOMA *

M. Seiji, Y. Tomita, Yasushi Tomita, 1977, The Journal of dermatology.

A point mutation in the tyrosinase gene of BALB/c albino mouse causing the cysteine----serine substitution at position 85.

S. Shibahara, M. Sato, H. Yamamoto, 1990, European journal of biochemistry.

Tyrosinase gene mutations causing oculocutaneous albinisms.

Y. Tomita, 1993, The Journal of investigative dermatology.

Molecular basis for the heterogeneity of human tyrosinase.

S. Shibahara, R. Müller, H. Tagami, 1988, The Tohoku journal of experimental medicine.

THE POSSIBLE PROCESSING OF TYROSINASE IN THE GOLGI COMPLEXES OF THE MELANOCYTE * **

M. Seiji, Y. Tomita, Yasushi Tomita, 1985, The Journal of dermatology.

Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene

S. Shibahara, K. Yasumoto, K. Yokoyama, 1994, Molecular and cellular biology.

Increase of pro-opiomelanocortin mRNA prior to tyrosinase, tyrosinase-related protein 1, dopachrome tautomerase, Pmel-17/gp100, and P-protein mRNA in human skin after ultraviolet B irradiation.

I. Suzuki, T. Katagiri, Y. Tomita, 2002, The Journal of investigative dermatology.

Effects of staurosporine, PMA and A23187 on human melanocyte cultures with dibutyryl cyclic AMP

H. Tagami, M. Fukuda, Y. Tomita, 1992, The British journal of dermatology.

A Splicing Mutation of the Tyrosinase Gene Causes Yellow Oculocutaneous Albinism in a Japanese Patient with a Pigmented Phenotype

M. Furue, Y. Miyamura, Y. Tomita, 1999, Dermatology.

The monoclonal antibodies TMH-1 and TMH-2 specifically bind to a protein encoded at the murine b-locus, not to the authentic tyrosinase encoded at the c-locus.

S. Shibahara, H. Tagami, S. Okinaga, 1991, The Journal of investigative dermatology.

Effect of pituitary and ovarian hormones on human melanocytes in vitro.

M. Fukuda, Y. Tomita, K. Maeda, 1996, Pigment cell research.

THE HYDROXYL RADICAL IS NOT INVOLVED WITH TYROSINASE INACTIVATION

A. Igarashi, M. Seiji, A. Igarashi, 1980, The Journal of dermatology.

Nature of tyrosinase inactivation in melanosomes.

M. Seiji, Y. Tomita, M. Sasaki, 1978, The Tohoku journal of experimental medicine.

Genetics of pigmentary disorders

Tamio Suzuki, Y. Tomita, 2004, American journal of medical genetics. Part C, Seminars in medical genetics.

Efficient culturing of human melanocytes from suction blisters.

H. Tagami, Y. Tomita, T. Takeuchi, 1985, Tohoku journal of experimental medicine.

Unilateral dermatomal pigmentary dermatosis: a variant dyschromatosis?

H. Tagami, Y. Tomita, M. Hara, 1992, Journal of the American Academy of Dermatology.

Cloning and sequence analysis of the tyrosinase gene from a patient with tyrosinase-positive oculocutaneous albinism.

S. Shibahara, H. Tagami, Y. Tomita, 1992, Journal of dermatological science.

Mechanisms for hyperpigmentation in postinflammatory pigmentation, urticaria pigmentosa and sunburn.

H. Tagami, H Tagami, Y Tomita, 1989, Dermatologica.

Six novel P gene mutations and oculocutaneous albinism type 2 frequency in Japanese albino patients.

H. Shimizu, Tamio Suzuki, O. Ishikawa, 2003, The Journal of investigative dermatology.

Five novel mutations in tyrosinase gene of Japanese and Indian patients with oculocutaneous albinism type I (OCA1).

I. Verma, R. Saxena, Tamio Suzuki, 2005, The Journal of investigative dermatology.

Polymorphic sequences of the tyrosinase gene: allele analysis on 16 OCA1 patients in Japan indicate that three polymorphic sequences in the tyrosinase gene promoter could be powerful markers for indirect gene diagnosis

H. Shimizu, H. Tagami, M. Kono, 2002, Journal of Human Genetics.

Km OF TYROSINASE IN MICROSOMES IS HIGHER THAN THAT IN MELANOSOMES

M. Seiji, Y. Tomita, A. Hariu, 1982, The Journal of dermatology.

Isolation and characterization of a Golgi-rich fraction from the Harding-Passey mouse melanoma.

M. Seiji, Y. Tomita, S. Moro, 1978, The Tohoku journal of experimental medicine.

Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes.

H. Shimizu, T. Okuyama, Tamio Suzuki, 2006, Pigment cell research.

A Korean case of oculocutaneous albinism type IV caused by a D157N mutation in the MATP gene

Y. Tomita, K. Inagaki, K. Fukai, 2005, The British journal of dermatology.

Messenger RNA levels of melanogenesis-associated genes in lentigo senilis lesions.

I. Suzuki, T. Katagiri, Y. Tomita, 2005, Journal of dermatological science.

Phospholipases Induce Melanogenesis in Organ‐Cultured Skin

Y. Tomita, K. Maeda, M. Naganuma, 1996, Photochemistry and photobiology.

Monoclonal antibodies produced against murine tyrosinase identify pigmented human melanocytes.

V. Hearing, Y. Tomita, 1986, Diagnostic immunology.

Electron microscopic DOPA reaction test for oculocutaneous albinism

H. Shimizu, T. Nishikawa, R. Aozaki, 2000, Archives of Dermatological Research.

The molecular genetics of albinism and piebaldism.

Y. Tomita, 1994, Archives of dermatology.

Inhibition of aminoacyl-transfer RNA formation by low-molecular substances from melanoma extract.

K. Tsutsumi, M. Seiji, T. Kato, 1984, Gan.

Two novel mutations detected in Japanese patients with oculocutaneous albinism.

Tamio Suzuki, M. Kono, S. Ito, 2006, Journal of dermatological science.

Molecular basis of tyrosinase-negative oculocutaneous albinism. A single base mutation in the tyrosinase gene causing arginine to glutamine substitution at position 59.

S. Shibahara, H. Tagami, Y. Tomita, 1990, The Journal of biological chemistry.

Molecular analysis of the DNA segments cross-hybridizable to the tyrosinase gene in patients affected with oculocutaneous albinism.

S. Shibahara, H. Tagami, Y. Tomita, 1989, The Tohoku journal of experimental medicine.

Genotype analysis in a patient with oculocutaneous albinism 1 minimal pigment type

K. Wakamatsu, M. Kono, T. Kondo, 2012, The British journal of dermatology.

Oculocutaneous albinism type IV: A boy of Moroccan descent with a novel mutation in SLC45A2

Tamio Suzuki, W. Courtens, K. Storm, 2009, American journal of medical genetics. Part A.

Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan.

H. Shimizu, Y. Umezawa, M. Takata, 2004, American journal of human genetics.

Molecular bases of congenital hypopigmentary disorders in humans and oculocutaneous albinism 1 in Japan.

M. Kono, Y. Miyamura, Y. Tomita, 2000, Pigment cell research.

Establishment of tyrosinase sequence database in normally pigmented Indians and Japanese for rapid determination of novel mutations.

I. Verma, R. Saxena, Tamio Suzuki, 2005, Journal of dermatological science.

A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1).

Y. Kano, M. Kono, Y. Miyamura, 2002, Journal of dermatological science.

Nucleotide sequence of the putative human tyrosinase pseudogene.

S. Shibahara, H. Tagami, Y. Tomita, 1991, The Tohoku journal of experimental medicine.

Detection of point mutations in human tyrosinase gene by improved allele‐specific amplification

H. Tagami, Y. Tomita, J. Matsunaga, 1995, Experimental dermatology.

Ten novel mutations of the ADAR1 gene in Japanese patients with dyschromatosis symmetrica hereditaria.

T. Horikawa, Y. Aoyama, Tamio Suzuki, 2007, The Journal of investigative dermatology.

Y. Tomita, A. Sakakibara, T. Ikeya, 2011, The Journal of dermatology.

Detection of Merkel cell polyomavirus in cutaneous squamous cell carcinoma before occurrence of Merkel cell carcinoma.

M. Akiyama, H. Katano, K. Yokota, 2011, Journal of the American Academy of Dermatology.

Functional analysis of OCA4 mutant sequences using under white mouse melanocytes

Tamio Suzuki, M. Kawaguchi, T. Kondo, 2009, Pigment cell & melanoma research.

Anti-DFS70 antibodies in 597 healthy hospital workers.

Yasushi Tomita, Y. Takasaki, E. Tan, 2004, Arthritis and rheumatism.

Giant superficial basal cell carcinoma of the scrotum.

Y. Tomita, H. Ishikawa, Y. Kato, 2005, European journal of dermatology : EJD.

Eight cases of malignant melanoma treated with inguinal and iliac lymph node dissection

Y. Tomita, A. Sakakibara, S. Shibata, 2005 .

Leukaemic dissemination of Merkel cell carcinoma in a patient with systemic lupus erythematosus

K. Natsuga, M. Kondo, H. Ujiie, 2008, Clinical and experimental dermatology.

Prediction of additional lymph node positivity and clinical outcome of micrometastases in sentinel lymph nodes in cutaneous melanoma: A multi‐institutional study of 450 patients in Japan

Yuhei Yamamoto, H. Iizuka, F. Otsuka, 2012, The Journal of dermatology.

Nodular Fasciitis of the Forehead in a Pediatric Patient

Y. Tomita, T. Asai, Y. Handa, 2003, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

Clinicopathologic analysis of 66 Japanese thin melanomas with metastasis of sentinel or regional lymph node

M. Akiyama, K. Yokota, M. Kono, 2013, Journal of cutaneous pathology.

A Case of Malignant Melanoma in the Right Sole with Sentinel Nodes Identified in Both the Right Inguinal and Popliteal Region.

Y. Tomita, Yasushi Ogawa, A. Sakakibara, 2001 .

Dowling–Degos disease with mutations in POFUT1 is clinicopathologically distinct from reticulate acropigmentation of Kitamura

M. Akiyama, D. Bodet, M. Kono, 2015, The British journal of dermatology.

High frequency of Hermansky-Pudlak syndrome type 1 (HPS1) among Japanese albinism patients and functional analysis of HPS1 mutant protein.

R. Spritz, H. Takiwaki, K. Takamori, 2005, The Journal of investigative dermatology.

A Patient with Subclinical Oculocutaneous Albinism Type 2 Diagnosed on Getting Severely Sunburned

M. Kawai, Tamio Suzuki, S. Ito, 2005, Dermatology.

Autoepitopes on autoantigen centromere protein‐A (CENP‐A) are restricted to the N‐terminal region, which has no homology with histone H3

M. Kunimatsu, K. Sugimoto, Y. Muro, 2000, Clinical and experimental immunology.

Dyschromatosis symmetrica hereditaria by ADAR1 mutations and viral encephalitis: a hidden link?

M. Akiyama, M. Kono, Y. Tomita, 2013, International journal of dermatology.

Ethnic Variability in the Plasma Exposures of OATP1B1 Substrates Such as HMG‐CoA Reductase Inhibitors: A Kinetic Consideration of Its Mechanism

Y. Sugiyama, Y Sugiyama, K Maeda, 2013, Clinical pharmacology and therapeutics.

A Case of Cutaneous Endometriosis Developing in the Pubis

Y. Tomita, S. Shibata, T. Iwai, 2004 .

A case of systemic lupus erythematosus: continued association of circulating prolactin levels with disease activity over a 4-year follow-up period

Y. Muro, K. Sugiura, Y. Tomita, 2005, Modern rheumatology.

[Thrombotic thrombocytopenic purpura with mixed connective tissue disease. A case report].

T. Naoe, A. Tomita, T. Matsushita, 2009, Arerugi = [Allergy].

Evaluation of anti-ribosomal P protein immunoassay in Japanese patients with connective tissue diseases: comparison with an indirect immunofluorescence assay

Y. Muro, K. Sugiura, Y. Tomita, 2009, Scandinavian journal of rheumatology.

Dystonia, mental deterioration, and dyschromatosis symmetrica hereditaria in a family with ADAR1 mutation

T. Hashimoto, Kunihiro Yoshida, S. Ikeda, 2006, Movement disorders : official journal of the Movement Disorder Society.

Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations.

M. Akiyama, Yasuhiro Suzuki, N. Matsumoto, 2016, The Journal of investigative dermatology.

Sunlight is merely a temporary modifier of dyschromatosis symmetrica hereditaria

M. Akiyama, M. Kono, Y. Miyamura, 2018, EJD. European journal of dermatology.

Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.

M. Kono, Y. Miyamura, Y. Tomita, 2000, Journal of dermatological science.

Four novel ADAR1 gene mutations in patients with dyschromatosis symmetrica hereditaria

M. Akiyama, M. Wataya-Kaneda, Tamio Suzuki, 2012, The Journal of dermatology.

Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria.

Y. Kubo, W. Fujimoto, T. Horikawa, 2009, Journal of dermatological science.

Mutation analyses of patients with dyschromatosis symmetrica hereditaria: five novel mutations of the ADAR1 gene.

A. Utani, Tamio Suzuki, N. Oiso, 2010, Journal of dermatological science.

Successful treatment of warts with a combination of maxacalcitol ointment and salicylic acid sticking plaster

Tamio Suzuki, Y. Tomita, A. Adachi, 2006, The Journal of dermatology.

Successful topical hemotherapy with a new occlusive dressing for an intractable ulcer on the toe

Y. Muro, K. Sugiura, Y. Tomita, 2009, The Journal of dermatology.

Diffuse Systemic Sclerosis with Severe Complications in Multiple Organs

Y. Muro, Y. Tomita, K. Omura, 2008 .

Angiotensin‐induced hypertension and chemotherapy for multiple lesions of malignant melanoma

Y. Tomita, H. Takematsu, T. Kato, 1985, The British journal of dermatology.

Autoantigenicity of DFS70 is restricted to the conformational epitope of C-terminal alpha-helical domain.

M. Kunimatsu, M. Mishima, Y. Muro, 2004, Journal of autoimmunity.

CENP-O, a Protein Localized at the Centromere Throughout the Cell Cycle, Is a Novel Target Antigen in Systemic Sclerosis

Yasushi Tomita, K. Yoda, M. Ikeno, 2009, The Journal of Rheumatology.

Investigation on the IVS5 +5G --> a splice site mutation of HPS1 gene found in Japanese patients with Hermansky-Pudlak syndrome.

T. Hashimoto, Tamio Suzuki, S. Ito, 2004, Journal of dermatological science.

Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.

M. Akiyama, Tamio Suzuki, K. Matsunaga, 2013, Human molecular genetics.

Dowling-Degos disease is genetically and clinico-pathologically distinct from reticulate acropigmentation of Kitamura, further confirmation

M. Akiyama, Tamio Suzuki, K. Matsunaga, 2016 .

Dominant dystrophic epidermolysis bullosa caused by a novel G2037R mutation and by a known G2028R mutation in the type VII collagen gene (COL7A1)

K. Tamai, H. Nakano, Y. Tomita, 2006, The Journal of dermatology.

Oculocutaneous albinism and analysis of tyrosinase gene in Japanese patients.

Y. Miyamura, Y. Tomita, 1998, Nagoya journal of medical science.

Evaluation of cetirizine hydrochloride-based therapeutic strategy for chronic urticaria.

Tamio Suzuki, T. Usuda, K. Sugiura, 2008, Nagoya journal of medical science.

Mucoepidermoid carcinoma with cutaneous infiltration similar to a subcutaneous cystic tumour

M. Sasaki, S. Shinkuma, Y. Tomita, 2009, Clincal and Experimental Dermatology.

A case of oral geotrichosis caused by Geotrichum capitatum in an old patient.

T. Kanbe, Y. Tomita, C. Inoue, 2007, Japanese journal of infectious diseases.

New primary malignant melanoma, epidermotropism and Indian-file arrangement of metastatic tumor cells in a case with intransit metastases of acral type of malignant melanoma.

H. Tagami, Y. Tomita, T. Demitsu, 1986, Dermatologica.

Steroid‐withdrawal Rosacea‐like Dermatitis

H. Tagami, Y. Tomita, 1989, The Journal of dermatology.

Primary cutaneous T‐cell lymphoma of unspecified type with cytotoxic phenotype: Clinicopathological analysis of 27 patients

K. Takata, T. Yoshino, Y. Tamada, 2009, Cancer science.

Epidermodysplasia verruciformis accompanied by familial large granular lymphocytosis and a decrease in T lymphocytes.

H. Tagami, S. Seki, Y. Tomita, 1993, Acta dermato-venereologica.