D. Sawamura

Hajime Nakano, Genji Imokawa, G. Imokawa, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Hair follicle stem cells provide a functional niche for melanocyte stem cells.

H. Nakauchi, J. R. McMillan, N. Binh, 2011, Cell stem cell.

In-frame Val216-Ser217 deletion of KIT in mild piebaldism causes aberrant secretion and SCF response.

K. Kaira, O. Ishikawa, D. Sawamura, 2018, Journal of dermatological science.

Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism.

H. Shimizu, Hideki Nakamura, D. Sawamura, 2004, Journal of dermatological science.

UVA Induced Darkening of Lower Epidermal Cells as an in vitro System of Immediate Pigment Darkening (IPD) and Mechanisms of IPD

I. Hashimoto, D. Sawamura, Y. Katabira, 1986, The Journal of dermatology.

Case of oculocutaneous albinism complicated with squamous cell carcinoma, Bowen's disease and actinic keratosis

H. Mizukami, Tamio Suzuki, Y. Matsuzaki, 2014, The Journal of dermatology.

Photoprotective effect of esterified glutathione against ultraviolet B-induced sunburn cell formation in the hairless mice.

K. Tamai, I. Hashimoto, K. Hanada, 1997, The Journal of investigative dermatology.

Cutaneous adenocarcinoma metastases associated with swelling of the neck and cheeks.

D. Sawamura, K. Yasukawa, S. Shimizu, 2004, Acta dermato-venereologica.

Squamous cell carcinoma arising from Darier's disease

T. Shimizu, T. Makino, D. Sawamura, 2009, Clinical and experimental dermatology.

A study of the steroid sulfatase gene in families with X-linked ichthyosis using polymerase chain reaction.

K. Tamai, K. Nomura, I. Hashimoto, 1995, Acta dermato-venereologica.

Treatment for poikilodermatous erythema of dermatomyositis with the pulsed dye laser

H. Shimizu, D. Sawamura, A. Shibaki, 2005, The British journal of dermatology.

Novel ATP2A2 nonsense mutation in a Japanese case with Darier's disease

D. Sawamura, H. Nakano, K. Fukai, 2021, The Journal of dermatology.

Transformation‐specific matrix metalloproteinases (MMP)‐7 and MMP‐13 are expressed by tumour cells in epidermolysis bullosa‐associated squamous cell carcinomas

H. Shimizu, J. McGrath, V. Kähäri, 2008, The British journal of dermatology.

A novel deletion mutation of the ATP2C1 gene in a family with Hailey-Hailey disease

M. Mizawa, T. Makino, K. Shimizu, 2016, European Journal of Dermatology.

External chalazion as reddish and intractable lower eyelid nodules in a child

D. Sawamura, H. Nakano, K. Nakajima, 2017, The Journal of dermatology.

CARD14 Glu138 mutation in familial pityriasis rubra pilaris does not warrant differentiation from familial psoriasis

T. Dainichi, K. Kabashima, D. Sawamura, 2016, The Journal of dermatology.

Significance of IL36RN mutation analyses in the management of impetigo herpetiformis: A case report and review of published cases

A. Kimura, Y. Yokoyama, D. Sawamura, 2021, The Journal of dermatology.

Detection of circulating lymphoma cells in subcutaneous panniculitis‐like T‐cell lymphoma

H. Shimizu, K. Yokota, D. Sawamura, 2003, The British journal of dermatology.

Blue Rubber Bleb Nevus Syndrome Showing Vascular Skin Lesions Predominantly on the Face

D. Sawamura, H. Nakano, T. Aizu, 2015, Case Reports in Dermatology.

Dermoscopy of eccrine poroma with calcification.

Y. Matsuzaki, Yohei Nishikawa, D. Sawamura, 2009, Journal of dermatological case reports.

Involvement of the histamine H1 receptor in the regulation of sympathetic nerve activity.

T. Yoshikawa, M. Murakami, T. Ohba, 2015, Biochemical and biophysical research communications.

Pediculus humanus capitis: Pyrethroid resistance and utility of scanning electron microscopy

Y. Matsuzaki, D. Sawamura, Sayaka Yamaguchi, 2019, Journal of dermatology (Print).

A novel ABCA12 mutation 3270delT causes harlequin ichthyosis

J. R. McMillan, M. Akiyama, H. Shimizu, 2006, The British journal of dermatology.

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.

Expression of the keratinocyte lipid transporter ABCA12 in developing and reconstituted human epidermis.

J. R. McMillan, M. Akiyama, H. Shimizu, 2007, The American journal of pathology.

The first case of multiple pilomatricomas caused by somatic mutations of CTNNB1 without any associated disorder.

D. Sawamura, H. Nakano, T. Aizu, 2017, Journal of dermatological science.

Immunosuppressive effect of adipose-derived stromal cells on imiquimod-induced psoriasis in mice.

Y. Matsuzaki, D. Sawamura, H. Nakano, 2016, Journal of dermatological science.

Subcutaneous dermoid cysts on the eyebrow and neck

D. Sawamura, H. Nakano, K. Nakajima, 2019, Pediatric dermatology.

Two cases of ichthyosis and their EPR analyses of stratum corneum

K. Nomura, Y. Matsuzaki, D. Sawamura, 2019, Journal of Cutaneous Immunology and Allergy.

Normolipidaemic xanthomatosis with systemic involvement of the skin, bone and pharynx

Y. Matsuzaki, D. Sawamura, H. Nakano, 2012, Clinical and experimental dermatology.

Case of epidermolytic palmoplantar keratoderma with knuckle pads

Tamio Suzuki, D. Sawamura, H. Nakano, 2012, The Journal of dermatology.

Scleroedema adultorum associated with sarcoidosis

H. Shimizu, D. Sawamura, R. Abe, 2009, Clinical and experimental dermatology.

Keratinocyte gene therapy: cytokine gene expression in local keratinocytes and in circulation by introducing cytokine genes into skin

K. Tamai, I. Hashimoto, K. Hanada, 2002, Experimental dermatology.

Successful treatment of Kyrle disease with narrowband ultraviolet B

Y. Matsuzaki, D. Sawamura, H. Nakano, 2017, The Journal of dermatology.

Incomplete erythropoietic protoporphyria caused by a splice site modulator homozygous IVS3‐48C polymorphism in the ferrochelatase gene

T. Shimizu, M. Mizawa, T. Makino, 2016, The British journal of dermatology.

Erythropoietic Protoporphyria in a Japanese Population.

M. Mizawa, T. Makino, D. Sawamura, 2019, Acta dermato-venereologica.

A Novel Humanized Neonatal Autoimmune Blistering Skin Disease Model Induced by Maternally Transferred Antibodies1

H. Shimizu, E. Olasz, K. Yancey, 2009, The Journal of Immunology.

Paraneoplastic syndrome associated with chronic myelogenous leukemia mimicking adult‐onset Still's disease

D. Sawamura, H. Nakano, K. Nakajima, 2019, The Journal of dermatology.

CD20+ primary cutaneous T‐cell lymphoma presenting as a solitary extensive plaque

Y. Matsuzaki, D. Sawamura, H. Nakano, 2009, The British journal of dermatology.

Contribution of dynamic sentinel lymphoscintigraphy images to the diagnosis of patients with malignant skin neoplasms in the upper and lower extremities

Y. Takai, D. Sawamura, K. Hirose, 2014, SpringerPlus.

Intralymphatic Histiocytosis with Rheumatoid Arthritis: Possible Association with the Joint Involvement

D. Sawamura, H. Nakano, T. Kaneko, 2014 .

Intravascular Histiocytosis Associated with Rheumatoid Arthritis

H. Shimizu, D. Sawamura, W. Nishie, 2008, Dermatology.

Usefulness of thermography techniques for evaluating the disease activity in Kimura’s disease

H. Shimizu, K. Natsuga, S. Aoyagi, 2008, Clinical and experimental dermatology.

Dominant dystrophic epidermolysis bullosa albopapuloidea Pasini -- ultrastructural observations of albopapuloid lesions and a type VII collagen DNA polymorphism study of a family.

K. Nomura, I. Hashimoto, D. Sawamura, 1997, Acta dermato-venereologica.

Bone marrow transplantation restores epidermal basement membrane protein expression and rescues epidermolysis bullosa model mice

J. R. McMillan, M. Akiyama, H. Shimizu, 2010, Proceedings of the National Academy of Sciences.

A case of penile malignant melanoma in a 93-year-old man

H. Shimizu, S. Aoyagi, H. Hata, 2003 .

Leuprorelin acetate granulomas: case reports and review of the literature

D. Sawamura, K. Yasukawa, H. Sugawara, 2005, The British journal of dermatology.

Amelanotic acral lentiginous melanoma mimicking diabetic ulcer: a challenge to diagnose and treat

D. Sawamura, H. Nakano, T. Kaneko, 2016, European Journal of Dermatology.

Pembrolizumab-Induced Lichen Planus on the Scalp of a Patient with Non-Small-Cell Lung Carcinoma

D. Sawamura, H. Nakano, E. Akasaka, 2021, Case Reports in Dermatology.

Fibroblasts show more potential as target cells than keratinocytes in COL7A1 gene therapy of dystrophic epidermolysis bullosa.

M. Akiyama, H. Shimizu, D. Sawamura, 2006, The Journal of investigative dermatology.

A Japanese family with dominant pretibial dystrophic epidermolysis bullosa: Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen.

T. Hashimoto, T. Hamada, D. Sawamura, 2009, Journal of dermatological science.

Annular leukocytoclastic vasculitis associated with essential mixed cryoglobulinemia

Y. Matsuzaki, D. Sawamura, H. Nakano, 2016, EJD. European journal of dermatology.

Modulation of Stimulator of Interferon Genes (STING) Expression by Interferon-γ in Human Keratinocytes

Y. Matsuzaki, Yohei Nishikawa, D. Sawamura, 2017, Biochemical Genetics.

The 6-year follow-up of a Japanese patient with silent erythropoietic protoporphyria

M. Mizawa, F. Furukawa, T. Makino, 2017, JAAD case reports.

Native Autoantigen Complex Detects Pemphigoid Autoantibodies

F. Schauer, K. Natsuga, D. Sawamura, 2023, JID innovations : skin science from molecules to population health.

Extracellular cleavage of collagen XVII is essential for correct cutaneous basement membrane formation.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2016, Human molecular genetics.

ITGB4 missense mutation in a transmembrane domain causes non-lethal variant of junctional epidermolysis bullosa with pyloric atresia.

H. Shimizu, Hideki Nakamura, H. Kawasaki, 2007, Journal of dermatological science.

The Inhibitory Effect of Selenium on Mice Inoculated with B16 Melanoma Cells

I. Hashimoto, K. Hanada, D. Sawamura, 1986, The Journal of dermatology.

A unique monoclonal antibody 29A stains the cytoplasm of amniotic epithelia and cutaneous basement membrane.

H. Shimizu, Y. Horiguchi, K. Kodama, 2006, Journal of dermatological science.

Expression of laminin, type IV procollagen and 230 kDa bullous pemphigoid antigen genes by keratinocytes and fibroblasts in culture: application of the polymerase chain reaction for detection of small amounts of messenger RNA

J. Uitto, K. Nomura, I. Hashimoto, 2004, Archives of Dermatological Research.

Multiple apocrine hidrocystoma showing plane pigmented macules.

H. Shimizu, D. Sawamura, A. Shibaki, 2006, Journal of American Academy of Dermatology.

Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA.

H. Sueki, D. Sawamura, H. Nakano, 2015, Journal of dermatological science.

Vörner type palmoplantar keratoderma: novel KRT9 mutation associated with knuckle pad‐like lesions and recurrent mutation causing digital mutilation

I. Katayama, N. Umegaki, D. Sawamura, 2011, The British journal of dermatology.

Instructions for use Title A novel ABCA 12 mutation 3270 delT causes harlequin ichthyosis

J. R. McMillan, H. Shimizu, I. Hausser, 2017 .

A Palindromic Motif in the −2084 to −2078 Upstream Region is Essential for ABCA12 Promoter Function in Cultured Human Keratinocytes

M. Akiyama, H. Shimizu, Jun-ichi Takeda, 2014, Scientific Reports.

Compound Heterozygous ABCA12 Mutations Including a Novel Nonsense Mutation Underlie Harlequin Ichthyosis

J. R. McMillan, M. Akiyama, H. Shimizu, 2007, Dermatology.

Low‐grade myxofibrosarcoma invaded into the underlying skeletal muscle

M. Akiyama, H. Shimizu, S. Aoyagi, 2007, The Journal of dermatology.

Cholesterotic fibrous histiocytoma with no associated dyslipidemia

Y. Matsuzaki, D. Sawamura, H. Nakano, 2017, International Journal of Dermatology.

Elephantiasis Nostras Verrucosa Successfully Treated by Surgical Debridement

H. Shimizu, D. Sawamura, K. Sato-Matsumura, 2004, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

Depigmented Macula as an Initial Manifestation of Extramammary Paget's Disease

I. Hashimoto, T. Yotsuyanagi, D. Sawamura, 1996, The Journal of dermatology.

Relation between the expression levels of the POU transcription factors Skn-1a and Skn-1n and keratinocyte differentiation.

K. Tamai, N. Umegaki, D. Sawamura, 2010, Journal of dermatological science.

Functional analysis of the nuclear localization signal of the POU transcription factor Skn‑1a in epidermal keratinocytes.

K. Tamai, D. Sawamura, H. Nakano, 2014, International journal of molecular medicine.

Stratum Corneum Structure of PsoriasisVulgaris Investigated by EPR Spin-Probe Method

D. Sawamura, K. Nakagawa, S. Minakawa, 2013 .

Spectroscopic evidence of abnormal structure of psoriasis vulgaris stratum corneum.

D. Sawamura, K. Nakagawa, S. Minakawa, 2012, Journal of dermatological science.

Vitamin D(3) inhibits expression of bullous pemphigoid antigen 1 through post-transcriptional mechanism without new protein synthesis.

K. Tamai, Y. Matsuzaki, D. Sawamura, 2008, Journal of dermatological science.

Identification of Skn-1n, a splice variant induced by high calcium concentration and specifically expressed in normal human keratinocytes.

J. Uitto, K. Tamai, T. Yamazaki, 2008, The Journal of investigative dermatology.

In vivo gene transfer method in keratinocyte gene therapy: intradermal injection of DNA complexed with high mobility group-1 protein in rats.

K. Tamai, I. Hashimoto, K. Hanada, 2000, Acta dermato-venereologica.

THE INTERACTION OF PHOTOPROTECTIVE EFFECTS BETWEEN KERATINOCYTES AND MELANOCYTES VIA ENDOTHELIN-1 / STEM CELL FACTOR SIGNALINGS

G. Imokawa, D. Sawamura, H. Nakano, 2012 .

Benign neonatal hemangiomatosis with early regression of skin lesions: A case report and review of the published work.

D. Sawamura, H. Nakano, K. Nakajima, 2020, The Journal of dermatology.

Disseminated lupus vulgaris diagnosed more than 63 years after onset due to early misdiagnosis as a port‐wine stain

Y. Matsuzaki, D. Sawamura, H. Nakano, 2010, Clinical and experimental dermatology.

Haber’s syndrome may be a clinical entity different from Dowling–Degos disease

T. Satoh, H. Yokozeki, D. Sawamura, 2009, The British journal of dermatology.

G2028R mutation in COL7A1 leads to marked heterogeneous clinical phenotypes of dominant dystrophic epidermolysis bullosa

H. Shimizu, T. Masunaga, J. Laduca, 2002 .

Two cases of folliculosebaceous cystic hamartoma

H. Shimizu, R. Abe, H. Kawasaki, 2006, Clinical and experimental dermatology.

COL7A1 mutation G2037E causes epidermal retention of type VII collagen

M. Akiyama, H. Shimizu, M. Furue, 2006, Journal of Human Genetics.

Role of beta-defensins in oral epithelial health and disease.

T. Kaku, Y. Abiko, M. Nishimura, 2007, Medical molecular morphology.

Elderly-Onset Generalized Pustular Psoriasis without a Previous History of Psoriasis Vulgaris

M. Akiyama, D. Sawamura, H. Nakano, 2015, Case Reports in Dermatology.

Subcutaneous histiocytoid Sweet's syndrome followed by acute myelocytic leukemia

D. Sawamura, H. Nakano, K. Nakajima, 2016, The Journal of dermatology.

p.Glu477Lys mutation in keratin 5 is not necessarily mortal in generalized severe epidermolysis bullosa simplex

T. Dainichi, K. Kabashima, A. Otsuka, 2018, The Journal of dermatology.

Small-diameter porous poly (epsilon-caprolactone) films enhance adhesion and growth of human cultured epidermal keratinocyte and dermal fibroblast cells.

J. R. McMillan, M. Akiyama, H. Shimizu, 2007, Tissue engineering.

Recurrent COL7A1 mutations in Japanese patients with dystrophic epidermolysis bullosa: positional effects of premature termination codon mutations on clinical severity. Japanese Collaborative Study Group on Epidermolysis Bullosa.

H. Shimizu, T. Nishikawa, J. Uitto, 1999, The Journal of investigative dermatology.

A Severe and Refractory Case of Anti-p200 Pemphigoid Resulting in Multiple Skin Ulcers and Scar Formation

M. Akiyama, H. Shimizu, T. Hashimoto, 2008, Dermatology.

Non‐Hodgkin lymphoma preceded by recalcitrant eczema

H. Shimizu, T. Koike, K. Natsuga, 2007, European journal of haematology.

Acute generalized exanthematous pustulosis due to hydroxychloroquine after a prolonged latent period

D. Sawamura, H. Nakano, T. Kaneko, 2018 .

Dystrophic epidermolysis bullosa pruriginosa successfully treated with immunosuppressants

Mitsuru Ito, M. Seishima, D. Sawamura, 2016, The Journal of dermatology.

Tegafur/gimeracil/oteracil (TS-1) induced Stevens–Johnson syndrome: Case report

Y. Matsuzaki, D. Sawamura, H. Nakano, 2013 .

Translucent basal cell carcinoma with a single cyst of the upper eyelid

D. Sawamura, H. Nakano, K. Nakajima, 2017, Journal of dermatology (Print).

Three cases of drug‐induced hypersensitivity syndrome associated with mRNA‐based coronavirus disease 2019 vaccines

D. Sawamura, H. Nakano, K. Nakajima, 2022, Journal of dermatology (Print).

Tuberculous granuloma developed 9 years after bacillus Calmette–Guérin vaccination in a patient with immunodeficiency

Y. Matsuzaki, D. Sawamura, K. Terui, 2018, The Journal of dermatology.

Hyper‐IgE syndrome with a novel mutation of the STAT3 gene

M. Akiyama, Y. Matsuzaki, Y. Minegishi, 2016, Clinical and experimental dermatology.

Psoriasis Area and Severity Index is closely related to serum C‐reactive protein level and neutrophil to lymphocyte ratio in Japanese patients

Y. Matsuzaki, D. Sawamura, T. Kaneko, 2017, The Journal of dermatology.

A 1,035-subject study suggesting a history of bone fracture as a possible factor associated with the development of anti-BP180 autoantibodies.

K. Sawada, S. Nakaji, D. Sawamura, 2021, The Journal of investigative dermatology.

Immunohistochemical analysis of in vivo UVB-induced secretion of IL-1α and IL-6 in keratinocytes.

Y. Matsuzaki, D. Sawamura, H. Nakano, 2011, Molecular medicine reports.

Mutations in FLG , the gene‐coding profilaggrin/filaggrin, are associated with putative hay fever in patients with atopic dermatitis

M. Akiyama, Y. Matsuzaki, D. Sawamura, 2020 .

A novel N14Y mutation in Connexin26 in keratitis-ichthyosis-deafness syndrome: analyses of altered gap junctional communication and molecular structure of N terminus of mutated Connexin26.

M. Akiyama, H. Shimizu, T. Aizawa, 2006, The American journal of pathology.

Partial anhidrosis demonstrated by Q‐SART in a patient with a novel mutation in the EDARADD gene

M. Wataya-Kaneda, I. Katayama, D. Sawamura, 2015, Journal of the European Academy of Dermatology and Venereology : JEADV.

Severe scoliosis associated with the WNT10A mutation

M. Wataya-Kaneda, I. Katayama, A. Tanemura, 2015, The Journal of dermatology.

A new EDA gene mutation in a family of X-linked hypohidrotic ectodermal dysplasia.

M. Seishima, D. Sawamura, H. Nakano, 2014, Journal of dermatological science.

Endoplasmic reticulum stress in the pathogenesis of pretibial dystrophic epidermolysis bullosa

K. Kaira, O. Ishikawa, D. Sawamura, 2017, The British journal of dermatology.

Case report: A case of epidermolysis bullosa acquisita with IgG and IgM anti-basement membrane zone antibodies relapsed after COVID-19 mRNA vaccination

H. Koga, T. Hashimoto, Y. Matsuzaki, 2023, Frontiers in Medicine.

Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib

D. Sawamura, H. Nakano, H. Kitamura, 2017, Case Reports in Dermatology.

Effect of Cepharanthin on Superoxide Anion (O2–) Production by Macrophages

K. Nomura, I. Hashimoto, K. Hanada, 1988, The Journal of dermatology.

Eruptive melanocytic nevi associated with encorafenib and cetuximab combination therapy

D. Sawamura, H. Nakano, E. Akasaka, 2022, The Journal of dermatology.

Ultraviolet B irradiation leads to the development of experimental bullous pemphigoid targeting BPAG1e.

H. Kijima, Y. Matsuzaki, D. Sawamura, 2022, Journal of dermatological science.

Incontinentia pigmenti in a male (XY) infant with long‐term follow up over 8 years

E. Ito, K. Nomura, Y. Matsuzaki, 2018, The Journal of dermatology.

Acquired cutis laxa secondary to acute generalized exanthematous pustulosis: A case report and mini-review of literature.

D. Sawamura, H. Nakano, E. Akasaka, 2023, The Journal of dermatology.

Spontaneous remission of methotrexateassociated lymphoproliferative disorder with Epstein-Barr virus type II latency

Y. Matsuzaki, D. Sawamura, H. Nakano, 2018, European Journal of Dermatology.

Hidradenitis suppurativa with perifolliculitis capitis abscedens et suffodiens successfully treated with a human anti‐tumour necrosis factor monoclonal antibody

Y. Matsuzaki, D. Sawamura, A. Kurose, 2021, Clinical and experimental dermatology.

Facial erythema alone as a manifestation of chronic graft-versus-host disease.

H. Shimizu, H. Hata, D. Sawamura, 2004, Acta dermato-venereologica.

A case of dominant dystrophic epidermolysis bullosa with diabetes mellitus presenting as progressive recalcitrant blisters and erosions

K. Kabashima, Y. Miyachi, D. Sawamura, 2014, International wound journal.

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.

Characterization of retinoic acid-inducible gene-I (RIG-I) expression corresponding to viral infection and UVB in human keratinocytes.

T. Imaizumi, K. Satoh, Y. Matsuzaki, 2012, Journal of dermatological science.

Two cases of the intermediate phenotype of recessive dystrophic epidermolysis bullosa harboring the novel COL7A1 mutation c.3570G>A.

D. Sawamura, H. Nakano, E. Akasaka, 2022, Journal of dermatological science.

Dystrophic epidermolysis bullosa pruriginosa of elderly onset

Tamio Suzuki, D. Sawamura, H. Nakano, 2011, The Journal of dermatology.

Leukemia cutis is an early sign of blast transformation that may mimic a common skin disease: Sycosis‐like eruptions in chronic myelomonocytic leukemia

Y. Matsuzaki, D. Sawamura, H. Nakano, 2010, The Journal of dermatology.

Identification of COL7A1 alternative splicing inserting 9 amino acid residues into the fibronectin type III linker domain.

M. Akiyama, H. Shimizu, D. Sawamura, 2003, The Journal of investigative dermatology.

The compound heterozygote for new/recurrent COL7A1 mutations in a Japanese patient with bullous dermolysis of the newborn.

T. Hashimoto, K. Tamai, T. Hamada, 2009, Journal of dermatological science.

The majority of keratinocytes incorporate intradermally injected plasmid DNA regardless of size but only a small proportion of cells can express the gene product.

H. Shimizu, K. Kodama, D. Sawamura, 2002, The Journal of investigative dermatology.

Recessive dystrophic epidermolysis bullosa: identification of a novel COL7A1 mutation of D44N.

E. Makino, W. Fujimoto, D. Sawamura, 2012, Journal of dermatological science (Amsterdam).

Bullous dermolysis of the newborn and dystrophic epidermolysis bullosa pruriginosa within the same family: two phenotypes associated with a COL7A1 mutation.

T. Hashimoto, M. Seishima, D. Sawamura, 2011, Acta dermato-venereologica.

Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen

H. Shimizu, G. Varigos, D. Murrell, 2011, The Australasian journal of dermatology.

A linear basal cell carcinoma undergoing spontaneous regression

D. Sawamura, H. Nakano, K. Kimura, 2009, Clincal and Experimental Dermatology.

Keratinocyte responsive element 3: analysis of a keratinocyte-specific regulatory sequence in the 230-kDa bullous pemphigoid antigen gene promoter.

J. Uitto, K. Tamai, I. Hashimoto, 2003, The Journal of investigative dermatology.

Bullous pemphigoid antigens (BPAGs): identification of RFLPs in human BPAG1 and BPAG2, and exclusion as candidate genes in a large kindred with dominant epidermolysis bullosa simplex.

J. Uitto, M. Ryynänen, R. Knowlton, 1991, Genomics.

Maternally Transferred Antibodies Blistering Skin Disease Model Induced by A Novel Humanized Neonatal Autoimmune

H. Shimizu, E. Olasz, K. Yancey, 2009 .

Decreased cardiac pacemaking and attenuated β-adrenergic response in TRIC-A knockout mice

H. Tomita, M. Nishi, H. Takeshima, 2020, PloS one.

Nagashima‐type palmoplantar keratoderma and malignant melanoma in Japanese patients

D. Sawamura, H. Nakano, T. Kaneko, 2018, The British journal of dermatology.

Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa: the splice site mutation c.6216+5G > T in the COL7A1 gene results in aberrant and normal splicings.

T. Hashimoto, T. Hamada, D. Sawamura, 2008, Journal of dermatological science.

Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa

H. Shimizu, Hideki Nakamura, D. Sawamura, 2005, Journal of Human Genetics.

The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa.

H. Shimizu, T. Masunaga, J. Laduca, 2004, Journal of dermatological science.

A novel insertion mutation in COL7A1 identified in Hallopeau-Siemens recessive dystrophic epidermolysis bullosa.

H. Shimizu, Hideki Nakamura, D. Sawamura, 2003, Acta dermato-venereologica.

Incontinentia pigmenti with retinal vascular anomaly and deletion of exons 4–10 in NEMO

H. Yamashita, Tamio Suzuki, D. Sawamura, 2017, The Journal of dermatology.

Follicular mucinosis associated with radiation therapy

Y. Matsuzaki, D. Sawamura, H. Takeda, 2011, The Journal of dermatology.

Atopic diathesis in hypohidrotic/anhidrotic ectodermal dysplasia.

M. Wataya-Kaneda, H. Murota, I. Katayama, 2015, Acta dermato-venereologica.

Sarcoidosis developing after stopping oral prednisolone for systemic lupus erythematosus.

D. Sawamura, T. Sugawara, K. Umeki, 2001, Acta dermato-venereologica.

Mild dystrophic epidermolysis bullosa associated with homozygous gene mutation c.6216+5G>T in type VII collagen ultrastructurally suggestive of the decreased number of anchoring fibrils

T. Dainichi, K. Kabashima, A. Otsuka, 2018, The Journal of dermatology.

Characterization of Stimulator of Interferon Genes (STING) Expression in Human Epidermal Keratinocytes [Innovation in Transplant and Regenerative Medicine. The 13th Meeting of Hirosaki International Forum of Medical Science. Communication Center of Hirosaki University School of Medicine. September 9

Y. Matsuzaki, Yohei Nishikawa, D. Sawamura, 2013 .

TGF-β1 Induces Fibroblast Proliferation Partly Through Actibation of RaF/MEK/ERK Signaling Pathway by Inhibition of RAF-KINASE Inhibitor Protein Expression

S. Tsuchida, K. Tamai, K. Hanada, 2016 .

Thymus and activation‐regulated chemokine elevation and lymphocytosis in a case of diffuse large B‐cell lymphoma

Y. Matsuzaki, D. Sawamura, T. Takahata, 2018 .

Dystrophic calcinosis cutis in a patient with cutaneous sarcoidosis in remission

D. Sawamura, Miyuki Yoshikawa, H. Nakano, 2022, Skin health and disease.

Keratinocyte gene therapy: inducible promoters and in vivo control of transgene expression

I. Hashimoto, D. Sawamura, K. Itai, 2001, Clinical and experimental dermatology.

Successful umbilical cord blood transplantation for intractable eczematous eruption in hypohidrotic ectodermal dysplasia with immunodeficiency

E. Ito, Y. Takahashi, D. Sawamura, 2009, Clincal and Experimental Dermatology.

Treatment of acquired reactive perforating collagenosis with 308‐nm excimer laser

D. Sawamura, H. Nakano, A. Matsui, 2016, Clinical and experimental dermatology.

Cerebrospinal fluid interleukin 8 concentrations and the subsequent development of postherpetic neuralgia.

A. Matsuki, D. Sessler, M. Yasujima, 2004, The American journal of medicine.

A case of lichen amyloidosis treated with pulsed dye laser

M. Akiyama, H. Shimizu, D. Sawamura, 2005, Journal of the European Academy of Dermatology and Venereology.

Analysis of the mechanism underlying a mild phenotype of hereditary coproporphyria due to a homozygous missense mutation in the transcription initiation codon of the coproporphyrinogen III oxidase gene.

K. Kabashima, Y. Matsuzaki, D. Sawamura, 2020, Journal of dermatological science (Amsterdam).

Squamous cell carcinoma developing in a 12‐year‐old boy with nonHallopeau–Siemens recessive dystrophic epidermolysis bullosa

H. Shimizu, H. Kawasaki, D. Sawamura, 2003, The British journal of dermatology.

Simultaneous occurrence of three squamous cell carcinomas in a recessive dystrophic epidermolysis bullosa patient.

H. Shimizu, D. Sawamura, K. Sato-Matsumura, 2003, Acta dermato-venereologica.

Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa

H. Shimizu, Hideki Nakamura, D. Sawamura, 2006, Journal of Human Genetics.

Response of epidermolysis bullosa fibroblasts to factors derived from macrophages and polymorphonuclear leukocytes in terms of collagenase production.

K. Nomura, I. Hashimoto, D. Sawamura, 1988, The Journal of investigative dermatology.

Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen.

H. Shimizu, H. Morioka, Gang Wang, 2010, The American journal of pathology.

Garlic‐induced irritant contact dermatitis mimicking nail psoriasis

Hajime Nakano, Kazuyuki Kimura, Y. Matsuzaki, 2011, The Journal of dermatology.

Late-onset, eruptive syringoma in an elderly man: correlation with carbamazepine.

Y. Matsuzaki, Yohei Nishikawa, D. Sawamura, 2012, Acta dermato-venereologica.

Giant cutaneous granular cell tumour with papillomatous appearance

D. Sawamura, H. Nakano, T. Kaneko, 2010, Clinical and experimental dermatology.

Angiolymphoid hyperplasia with eosinophilia in infancy

D. Sawamura, H. Nakano, T. Kaneko, 2012, The Journal of dermatology.

Novel gross deletion mutation c.‐105_4042+498del in the TNXB gene in a Japanese woman with classical‐like Ehlers–Danlos syndrome: A case of uneventful pregnancy and delivery

M. Itoh, D. Sawamura, O. Samura, 2021, The Journal of dermatology.

Actinic granuloma associated with erythema nodosum.

Y. Matsuzaki, Yohei Nishikawa, D. Sawamura, 2011, EJD. European journal of dermatology.

A case of COVID‐19 with pernio‐like skin lesions and increased red blood cell distribution width

Y. Matsuzaki, D. Sawamura, S. Minakawa, 2022, Journal of Cutaneous Immunology and Allergy.

Exon 87 skipping of the COL7A1 gene in dominant dystrophic epidermolysis bullosa

H. Koga, T. Hashimoto, T. Hamada, 2011, The Journal of dermatology.

A Novel Active Mouse Model for Bullous Pemphigoid Targeting Humanized Pathogenic Antigen

M. Akiyama, H. Shimizu, Gang Wang, 2010, Journal of Immunology.

Analysis of the COL17A1 in non-Herlitz junctional epidermolysis bullosa and amelogenesis imperfecta.

H. Shimizu, T. Ariga, Y. Sakiyama, 2006, International journal of molecular medicine.

Remodeling of desmosomal and hemidesmosomal adhesion systems during human hair follicle development.

M. Akiyama, H. Shimizu, D. Sawamura, 2004, Journal of dermatological science.

Reduction in epidermal Langerhans cells in patients with necrolytic migratory erythema.

T. Kusumi, Y. Tando, N. Umegaki, 2008, Journal of dermatological science.

Dipeptidyl peptidase‐4 inhibitor‐associated anti‐laminin‐γ1 (p200) pemphigoid in a patient with psoriasis vulgaris

T. Hashimoto, Y. Matsuzaki, D. Sawamura, 2020, The Journal of dermatology.

A diagnostically challenging case of tuberculous lymphadenitis

D. Sawamura, T. Takahata, T. Kaneko, 2016 .

Anti‐p200 pemphigoid in a 17‐year‐old girl successfully treated with systemic corticosteroid and dapsone

H. Shimizu, T. Hashimoto, K. Kodama, 2007, The British journal of dermatology.

Elevated levels of circulating immunoglobulin E autoantibodies against BP180 and BP230 in an intractable case of bullous pemphigoid.

D. Sawamura, H. Nakano, E. Akasaka, 2016, Journal of dermatological science.

Usefulness of ultrasonography in the diagnosis of ischaemic fasciitis

D. Sawamura, H. Nakano, T. Kaneko, 2016, Clinical and experimental dermatology.

Inhibitory Effect of TGF-β on Expression of 230KD Bullous Pemphigoid Antigen

K. Tamai, I. Hashimoto, K. Hanada, 2007 .

Genomic organization of collagenous domains and chromosomal assignment of human 180-kDa bullous pemphigoid antigen-2, a novel collagen of stratified squamous epithelium.

J. Uitto, M. Mattei, D. Sawamura, 1991, Journal of Biological Chemistry.

Assessment of a Case of Immediate-Type Allergy against Human Insulin in a Type 2 Diabetic Patient and Allergic Reactions to Human Insulin in Japan

D. Sawamura, T. Kaneko, N. Takiyoshi, 2014 .

Epistatic connections between microphthalmia‐associated transcription factor and endothelin signaling in Waardenburg syndrome and other pigmentary disorders

G. Imokawa, Jinyan Du, K. Hanada, 2008, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Response of intractable skin ulcers in recessive dystrophic epidermolysis bullosa patients to an allogeneic cultured dermal substitute.

M. Akiyama, H. Shimizu, K. Natsuga, 2010, Acta dermato-venereologica.

Novel mutation in a fumalate hydratase gene of a Japanese patient with multiple cutaneous and uterine leiomyomatosis.

H. Shimizu, T. Makino, D. Sawamura, 2007, Journal of dermatological science.

Novel function of metallothionein in photoprotection: metallothionein-null mouse exhibits reduced tolerance against ultraviolet B injury in the skin.

N. Miura, A. Naganuma, K. Tamai, 1998, The Journal of investigative dermatology.

Hailey-Hailey disease diagnosed based on an exacerbation of contact dermatitis with topical crotamiton

M. Mizawa, T. Makino, D. Sawamura, 2014, EJD. European journal of dermatology.

Garlic‐induced irritant contact dermatitis mimicking nail psoriasis

Y. Matsuzaki, D. Sawamura, H. Nakano, 2011, Journal of dermatology (Print).