W. Nishie

发表

Long-term follow-up of cultured epidermal autograft in a patient with recessive dystrophic epidermolysis bullosa.

H. Shimizu, H. Kawasaki, D. Sawamura, 2014, Acta dermato-venereologica.

In vitro and in vivo models to investigate the pathomechanisms and novel treatments for pemphigoid diseases

H. Koga, K. Bieber, W. Nishie, 2017, Experimental dermatology.

Follicular germinative cells in pilomatricoma.

W. Nishie, Tetsunori Kimura, 2006, The American Journal of dermatopathology.

Birt–Hogg–Dubé syndrome with clear‐cell and oncocytic renal tumour and trichoblastoma associated with a novel FLCN mutation

H. Shimizu, K. Urabe, A. Yokomizo, 2009, The British journal of dermatology.

Ramucirumab-induced Multiple Haemangiomas of the Skin: Two Case Reports.

H. Shimizu, Y. Kitamura, Hiroyuki Nakamura, 2018, Acta dermato-venereologica.

“Sprinkle brightness lesion” appearance in ultrasound B‐mode findings of sinusoidal hemangioma

H. Shimizu, H. Hata, W. Nishie, 2014, The Journal of dermatology.

BP180 Autoantibodies Target Different Epitopes in Multiple Sclerosis or Alzheimer's Disease than in Bullous Pemphigoid.

H. Shimizu, S. Herukka, K. Tasanen, 2019, The Journal of investigative dermatology.

Pyoderma gangrenosum associated with Takayasu's arteritis

H. Shimizu, K. Yokota, D. Sawamura, 2004, Clinical and experimental dermatology.

MOB1-YAP1/TAZ-NKX2.1 axis controls bronchioalveolar cell differentiation, adhesion and tumour formation

T. Sasaki, K. Nakao, K. Mimori, 2017, Oncogene.

The β9 loop domain of PA-PLA1α has a crucial role in autosomal recessive woolly hair/hypotrichosis.

M. Akiyama, H. Shimizu, J. Aoki, 2012, The Journal of investigative dermatology.

Pemphigoid Model Activation in Experimental Bullous Domain Induces Blisters via Complement Human Collagen 17 Noncollagenous 16A Human IgG1 Monoclonal Antibody against

H. Shimizu, K. Natsuga, Gang Wang, 2010 .

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

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

Regulatory T‐cell dysfunction induces autoantibodies to bullous pemphigoid antigens in mice and human subjects

H. Shimizu, I. Kobayashi, K. Natsuga, 2018, The Journal of allergy and clinical immunology.

Type XVII collagen is a key player in tooth enamel formation.

M. Akiyama, H. Shimizu, K. Natsuga, 2009, The American journal of pathology.

Animal models of epidermolysis bullosa.

H. Shimizu, K. Natsuga, S. Shinkuma, 2010, Dermatologic clinics.

Preferential Reactivity of Dipeptidyl Peptidase-IV Inhibitor-Associated Bullous Pemphigoid Autoantibodies to the Processed Extracellular Domains of BP180

H. Shimizu, K. Izumi, W. Nishie, 2019, Front. Immunol..

Gliptin-Associated Bullous Pemphigoid: A Valuable Model of the Mechanism of Breakdown of Immune Tolerance against BP180.

K. Tasanen, W. Nishie, 2019, The Journal of investigative dermatology.

Dipeptidyl peptidase IV inhibitor-associated bullous pemphigoid: a recently recognized autoimmune blistering disease with unique clinical, immunological and genetic characteristics

W. Nishie, 2019, Immunological medicine.

Somatic recombination underlies frequent revertant mosaicism in loricrin keratoderma

M. Akiyama, H. Shimizu, A. Ishida-Yamamoto, 2019, Life Science Alliance.

Morphological and genetic analysis of steatocystoma multiplex in an Asian family with pachyonychia congenita type 2 harbouring a KRT17 missense mutation

M. Akiyama, H. Shimizu, T. Shimizu, 2009, The British journal of dermatology.

[Clinical and molecular findings of pachyonychia congenita type 2 (PC-2)].

H. Shimizu, K. Natsuga, W. Nishie, 2015, Gaceta medica de Mexico.

Granzyme B inhibition reduces disease severity in autoimmune blistering diseases

A. Burleigh, H. Shimizu, N. Van Laeken, 2021, Nature communications.

Epitope-Dependent Pathogenicity of Antibodies Targeting a Major Bullous Pemphigoid Autoantigen Collagen XVII/BP180.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2016, The Journal of investigative dermatology.

The different intensity of autoantibody deposits in bullous pemphigoid associated with psoriasis vulgaris

H. Shimizu, H. Iwata, C. Nakayama, 2015, European Journal of Dermatology.

Doxycycline-Inducible Autoimmune Blistering Skin Disease Model

H. Shimizu, W. Nishie, 2015 .

Bullous Pemphigoid ( BP ) , The Most Common Autoimmune Blistering Disease

H. Shimizu, W. Nishie, 2015 .

Antibodies to Pathogenic Epitopes on Type XVII Collagen Cause Skin Fragility in a Complement-Dependent and -Independent Manner

H. Shimizu, K. Natsuga, D. Sawamura, 2012, The Journal of Immunology.

Pathogenesis of bullous pemphigoid.

H. Shimizu, H. Ujiie, W. Nishie, 2012, Immunology and allergy clinics of North America.

MannerComplement-Dependent and -Independent XVII Collagen Cause Skin Fragility in a Antibodies to Pathogenic Epitopes on Type

Hiroshi, K. Natsuga, D. Sawamura, 2012 .

Pathogenesis of bullous pemphigoid.

H. Shimizu, H. Ujiie, W. Nishie, 2011, Dermatologic clinics.

Deep venous thrombosis in patients with Behçet's disease

H. Shimizu, T. Nomura, K. Izumi, 2015, The Journal of dermatology.

Molecular Pathogenesis of Genetic and Inherited Diseases Keratinocyte-/ Fibroblast-Targeted Rescue of Col 7 a 1-Disrupted Mice and Generation of an Exact Dystrophic Epidermolysis Bullosa Model Using a Human COL 7 A 1 Mutation

M. Akiyama, H. Shimizu, J. Uitto, 2010 .

Plectin Deficiency Leads to Both Muscular Dystrophy and Pyloric Atresia in Epidermolysis Bullosa Simplex

H. Shimizu, H. Osaka, Hideki Nakamura, 2010, Human mutation.

Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex

J. R. McMillan, M. Akiyama, H. Shimizu, 2010, Human mutation.

CD44-Deficient Mice Do Not Exhibit Impairment of Epidermal Langerhans Cell Migration to Lymph Nodes after Epicutaneous Sensitization with Protein

M. Akiyama, H. Shimizu, Hideki Nakamura, 2010 .

Hidradenoma papilliferum with mixed histopathologic features of syringocystadenoma papilliferum and anogenital mammary‐like glands

H. Shimizu, D. Sawamura, W. Nishie, 2004, Journal of cutaneous pathology.

DNA‐based prenatal diagnosis of plectin‐deficient epidermolysis bullosa simplex associated with pyloric atresia

J. R. McMillan, M. Akiyama, H. Shimizu, 2011, International journal of dermatology.

The differences of collagen XVII between the oral mucosa and the skin discover the pathogenesis of oral lesions in pemphigoid

H. Shimizu, K. Natsuga, Y. Kitagawa, 2020 .

High Expression of Collagen XVII Compensates for its Depletion Induced by Pemphigoid IgG in the Oral Mucosa.

H. Shimizu, K. Natsuga, Y. Kitagawa, 2018, The Journal of investigative dermatology.

C-Terminal Processing of Collagen XVII Induces Neoepitopes for Linear IgA Dermatosis Autoantibodies.

H. Shimizu, W. Fujimoto, K. Natsuga, 2017, The Journal of investigative dermatology.

A recurrent 'hot spot' glycine substitution mutation, G2043R in COL7A1, induces dominant dystrophic epidermolysis bullosa associated with intracytoplasmic accumulation of pro-collagen VII.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2014, Journal of dermatological science.

Ectodomain Shedding Generates Neoepitopes on Collagen XVII, the Major Autoantigen for Bullous Pemphigoid

J. Jacków, A. Schlosser, Claus-Werner Franzke, 2010, The Journal of Immunology.

Bullous Pemphigoid for on Collagen XVII, the Major Autoantigen Ectodomain Shedding Generates Neoepitopes

J. Jacków, A. Schlosser, Claus-Werner Franzke, 2010 .

Intravenous IgG Reduces Pathogenic Autoantibodies, Serum IL-6 Levels, and Disease Severity in Experimental Bullous Pemphigoid Models.

H. Shimizu, K. Natsuga, S. Shinkuma, 2018, The Journal of investigative dermatology.

Unique clinical and serological features of bullous pemphigoid associated with dipeptidyl peptidase‐4 inhibitors

H. Shimizu, H. Itoh, M. Amagai, 2018, The British journal of dermatology.

Autoantibody Profile Differentiates between Inflammatory and Noninflammatory Bullous Pemphigoid.

H. Shimizu, K. Natsuga, K. Izumi, 2016, The Journal of investigative dermatology.

In vivo analysis of IgE autoantibodies in bullous pemphigoid: a study of 100 cases.

H. Shimizu, K. Natsuga, H. Ujiie, 2015, Journal of dermatological science.

Targeted skipping of a single exon harboring a premature termination codon mutation: implications and potential for gene correction therapy for selective dystrophic epidermolysis bullosa patients.

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

A case of anti-BP230 antibody-positive bullous pemphigoid receiving DPP-4 inhibitor

H. Shimizu, K. Sawada, T. Matsushita, 2020, Immunological medicine.

Clinical and genetic analysis of Fabry disease: report of six cases including three heterozygous females.

H. Shimizu, E. Noguchi, D. Sawamura, 2008, Journal of dermatological science.

Skipped exon in COL7A1 determines the clinical phenotypes of dystrophic epidermolysis bullosa

H. Shimizu, M. Komine, M. Ohtsuki, 2015, The British journal of dermatology.

HLA-DQB1*03:01 as a Biomarker for Genetic Susceptibility to Bullous Pemphigoid Induced by DPP-4 Inhibitors.

T. Mushiroda, H. Shimizu, H. Miyoshi, 2017, The Journal of investigative dermatology.

Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA‐PLA1α in autosomal recessive hypotrichosis

M. Akiyama, H. Shimizu, J. Aoki, 2010, Human mutation.

Fc‐binding proteins enhance autoantibody‐induced BP180 depletion in pemphigoid

H. Shimizu, K. Natsuga, H. Ujiie, 2019, The Journal of pathology.

A Case of Follicular Lymphoma with Cutaneous Infiltration.

S. Kano, W. Nishie, T. Ishihara, 2002 .

Sarcomatoid carcinoma of the liver with skin and pleural metastases

W. Nishie, T. Kusama, T. Koshiyama, 2003, The British journal of dermatology.

Humanization of autoantigen

J. R. McMillan, M. Akiyama, H. Shimizu, 2007, Nature Medicine.

Rituximab therapy for refractory autoimmune bullous diseases: A multicenter, open‐label, single‐arm, phase 1/2 study on 10 Japanese patients

H. Shimizu, M. Amagai, T. Hashimoto, 2019, The Journal of dermatology.

Type XVII collagen interacts with the aPKC‐PAR complex and maintains epidermal cell polarity

H. Shimizu, K. Natsuga, Tomonori Hirose, 2020, Experimental dermatology.

Japanese guidelines for the management of pemphigoid (including epidermolysis bullosa acquisita)

H. Shimizu, W. Fujimoto, M. Amagai, 2019, The Journal of dermatology.

Subepidermal blistering disease with 3 distinct autoantibodies: anti-BP230, anti-laminin gamma-1, and anti-laminin-332.

H. Shimizu, K. Natsuga, S. Shinkuma, 2011, Journal of the American Academy of Dermatology.

Complete paternal isodisomy of chromosome 17 in junctional epidermolysis bullosa with pyloric atresia.

M. Akiyama, H. Shimizu, Hideki Nakamura, 2010, The Journal of investigative dermatology.

Acquired Haemophilia A in DPP4 Inhibitor-induced Bullous Pemphigoid as Immune Reconstitution Syndrome

Y. Aoyama, K. Izumi, H. Hayashi, 2020, Acta dermato-venereologica.

Progressive refractory ulcer of the nipple: a quiz.

M. Akiyama, H. Shimizu, W. Nishie, 2009, Acta dermato-venereologica.

Primary cutaneous diffuse large B‐cell lymphoma presenting as a solitary subcutaneous nodule with TP53 and FBXW7 mutations

H. Shimizu, H. Nishihara, K. Fujii, 2017, International journal of dermatology.

Infantile eczema caused by formula milk

H. Shimizu, R. Abe, Y. Fujita, 2013, The Lancet.

Update on the pathogenesis of bullous pemphigoid: an autoantibody-mediated blistering disease targeting collagen XVII.

W. Nishie, 2014, Journal of dermatological science.

Childhood epidermolysis bullosa acquisita with autoantibodies against the noncollagenous 1 and 2 domains of type VII collagen: case report and review of the literature

M. Akiyama, H. Shimizu, T. Hashimoto, 2006, The British journal of dermatology.

Circulating IgA and IgE autoantibodies in antilaminin‐332 mucous membrane pemphigoid

H. Shimizu, T. Hashimoto, K. Natsuga, 2010, The British journal of dermatology.

Autoantibodies against type XVII collagen C‐terminal domain in a patient with bullous pemphigoid associated with psoriasis vulgaris

H. Shimizu, T. Hashimoto, K. Natsuga, 2009, The British journal of dermatology.

Bullous pemphigoid associated with psoriasis showing marked neutrophilic infiltrates

H. Shimizu, H. Hata, H. Ujiie, 2020, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.

Development of an ELISA for sensitive and specific detection of IgA autoantibodies against BP180 in pemphigoid diseases

T. Hashimoto, M. Hertl, L. Bruckner-Tuderman, 2011, Orphanet journal of rare diseases.

Oral mucosa is a useful substrate for detecting autoantibodies of mucous membrane pemphigoid

H. Shimizu, K. Natsuga, Y. Kitagawa, 2018, The British journal of dermatology.

Intraepidermal neutrophilic IgA pemphigus successfully treated with dapsone.

H. Shimizu, T. Nomura, R. Abe, 2012, European journal of dermatology : EJD.

Collagen XVII participates in keratinocyte adhesion to collagen IV, and in p38MAPK-dependent migration and cell signaling.

J. R. McMillan, M. Akiyama, H. Shimizu, 2009, The Journal of investigative dermatology.

Cutaneous pemphigus vulgaris with skin features similar to the classic mucocutaneous type: a case report and review of the literature

H. Shimizu, M. Amagai, K. Natsuga, 2008, Clinical and experimental dermatology.

Dynamic interactions of epidermal collagen XVII with the extracellular matrix: laminin 332 as a major binding partner.

L. Bruckner-Tuderman, A. Nyström, D. Kiritsi, 2011, The American journal of pathology.

Dipeptidyl peptidase‐4 inhibitors‐associated bullous pemphigoid: A retrospective study of 168 pemphigoid and 9,304 diabetes mellitus patients

H. Shimizu, H. Arima, H. Sobajima, 2018, Journal of diabetes investigation.

The direct binding of collagen XVII and collagen IV is disrupted by pemphigoid autoantibodies

H. Shimizu, K. Natsuga, Y. Kitagawa, 2018, Laboratory Investigation.

BJD-2005-01478 Revised Version Case Report Childhood epidermolysis bullosa acquisita with autoantibodies against the non-collagenous 1 and 2 domains of type VII collagen : a case report and a review of the literature

M. Akiyama, H. Shimizu, T. Hashimoto, 2017 .

Bullous Pemphigoid Triggered by Thermal Burn Under Medication With a Dipeptidyl Peptidase-IV Inhibitor: A Case Report and Review of the Literature

H. Shimizu, K. Izumi, W. Nishie, 2018, Front. Immunol..

Paper-based ELISA for the detection of autoimmune antibodies in body fluid-the case of bullous pemphigoid.

Hiroshi Shimizu, Chao-Min Cheng, Hsi-Kai Wang, 2014, Analytical chemistry.

Congenital nevi with hypomelanosis and fine scales

H. Shimizu, A. Kawada, Hideki Nakamura, 2019, European Journal of Dermatology.

What’s new in bullous pemphigoid

H. Shimizu, A. Shibaki, H. Ujiie, 2010, The Journal of dermatology.

Detection of mucous membrane pemphigoid autoantibodies by full-length BP180 enzyme-linked immunosorbent assay.

H. Shimizu, K. Natsuga, K. Izumi, 2017, Journal of dermatological science.

Two cases of erosive oral lichen planus with autoantibodies to desmoglein 3

H. Shimizu, Tamaki Yamada, K. Natsuga, 2016, The Journal of dermatology.

Dipeptidyl Peptidase-4 Inhibitor-Associated Bullous Pemphigoid

K. Tasanen, W. Nishie, O. Varpuluoma, 2019, Front. Immunol..

Multiple nodules on the face and in the nasal cavity are the symptoms of vegetative pyoderma gangrenosum complicated with myelodysplastic syndrome

W. Nishie, K. Ohnishi, K. Sato-Matsumura, 2006, Clinical and experimental dermatology.

Sweet's Syndrome Evolved from Recurrent Erythema Nodosum in a Patient with Myelodysplastic Syndrome

W. Nishie, Tetsunori Kimura, M. Kanagawa, 2002, The Journal of dermatology.

Widespread erythema ab igne caused by hot bathing

H. Shimizu, H. Iwata, S. Takashima, 2015, Journal of the European Academy of Dermatology and Venereology : JEADV.

Plasma cell cheilitis successfully treated with topical calcineurin inhibitors

H. Shimizu, W. Nishie, T. Ito, 2016, European Journal of Dermatology.

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

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

Life before and beyond blistering: The role of collagen XVII in epidermal physiology

H. Shimizu, K. Natsuga, W. Nishie, 2018, Experimental dermatology.

Type XVII collagen coordinates proliferation in the interfollicular epidermis

F. Watt, H. Shimizu, Giacomo Donati, 2017, eLife.

Chromosomal inversions as a hidden disease-modifying factor for somatic recombination phenotypes.

M. Akiyama, H. Shimizu, T. Nomura, 2018, JCI insight.

Autoantibody profile differentiates between inflammatory and non-inflammatory bullous pemphigoid

H. Shimizu, K. Natsuga, K. Izumi, 2016 .

A possible association between BP230‐type bullous pemphigoid and dementia: a report of two cases in elderly patients

H. Shimizu, K. Izumi, M. Zheng, 2018, The British journal of dermatology.

Macropinocytosis of type XVII collagen induced by bullous pemphigoid IgG is regulated via protein kinase C

H. Shimizu, K. Natsuga, K. Izumi, 2016, Laboratory Investigation.

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

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

Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects.

M. Akiyama, H. Shimizu, H. Nishihara, 2008, Human molecular genetics.

Consequences of two different amino-acid substitutions at the same codon in KRT14 indicate definitive roles of structural distortion in epidermolysis bullosa simplex pathogenesis.

Brian J. Smith, M. Akiyama, H. Shimizu, 2011, The Journal of investigative dermatology.

Bullous Pemphigoid Autoantibodies Directly Induce Blister Formation without Complement Activation

H. Shimizu, Hideki Nakamura, K. Natsuga, 2014, The Journal of Immunology.

Noncollagenous 16A domain of type XVII collagen-reactive CD4+ T cells play a pivotal role in the development of active disease in experimental bullous pemphigoid model.

H. Shimizu, A. Shibaki, S. Shinkuma, 2012, Clinical immunology.

Human IgG1 Monoclonal Antibody against Human Collagen 17 Noncollagenous 16A Domain Induces Blisters via Complement Activation in Experimental Bullous Pemphigoid Model

H. Shimizu, H. Morioka, Gang Wang, 2010, The Journal of Immunology.

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.

Intravascular Histiocytosis Associated with Rheumatoid Arthritis

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

Case of hereditary leiomyomatosis and renal cell cancer showing multiple cutaneous leiomyomas harboring a recurrent nonsense mutation in the fumarate hydratase gene

H. Ujiie, W. Nishie, K. Arita, 2021, The Journal of 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.

Early severe pachyonychia congenita subtype PC‐K6a with a novel mutation in the KRT6A gene

H. Shimizu, E. Bellacchio, K. Natsuga, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

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.

Dermoscopic observation in adenoma of the nipple

H. Shimizu, T. Nomura, Y. Fujita, 2015, The Journal of dermatology.

A subcutaneous tumor on the forehead of a 12-year-old child: a rare clinical presentation of a frontal mucocele.

M. Akiyama, H. Shimizu, W. Nishie, 2004, Journal of the American Academy of 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.

Highly prevalent SERPINB7 founder mutation causes pseudodominant inheritance pattern in Nagashima‐type palmoplantar keratosis

M. Akiyama, H. Shimizu, T. Nomura, 2014, The British journal of dermatology.

Coiled Coils Ensure the Physiological Ectodomain Shedding of Collagen XVII*

J. Jacków, Claus-Werner Franzke, L. Bruckner-Tuderman, 2012, The Journal of Biological Chemistry.

Simultaneous development of cutaneous vasculitis and an autoimmune bullous skin disease during anti-TNF therapy for rheumatoid arthritis: a case report and review of the literature

H. Shimizu, K. Ohmura, T. Mimori, 2018 .

Autoantibodies of non‐inflammatory bullous pemphigoid hardly deplete type XVII collagen of keratinocytes

H. Shimizu, K. Natsuga, K. Izumi, 2017, Experimental dermatology.

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.

A founder effect of c.1938delC in ITGB4 underlies junctional epidermolysis bullosa and its application for prenatal testing

M. Akiyama, H. Shimizu, T. Kusaka, 2011, Experimental dermatology.

Subepidermal autoimmune bullous disease affecting predominantly mucocutaneous junctions and the palms with autoantibodies to BP230 and laminin γ1

T. Dainichi, K. Kabashima, Y. Miyachi, 2016, The British journal of dermatology.

Loss of interaction between plectin and type XVII collagen results in epidermolysis bullosa simplex

H. Shimizu, Hideki Nakamura, K. Natsuga, 2017, Human mutation.

Multiple apocrine hidrocystoma showing plane pigmented macules.

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

A case of idiopathic angioedema exacerbated by angiotensin receptor blocker administration

H. Shimizu, W. Nishie, Y. Ohguchi, 2017, International journal of dermatology.

Bullous pemphigoid suggestive of complement‐independent blister formation with anti‐BP180 IgG4 autoantibodies

T. Dainichi, K. Kabashima, H. Ujiie, 2016, The British journal of dermatology.

A severe case of mango dermatitis

H. Shimizu, H. Hata, H. Miyazawa, 2018, Journal of the European Academy of Dermatology and Venereology : JEADV.

Successful treatment of severe recalcitrant erosive oral lichen planus with topical tacrolimus

H. Shimizu, A. Shibaki, W. Nishie, 2006, Journal of the European Academy of Dermatology and Venereology : JEADV.

Hair follicle stem cell progeny heal blisters while pausing skin development

H. Shimizu, Yasuaki Kobayashi, Hideki Nakamura, 2020, bioRxiv.

Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome.

H. Shimizu, M. Komine, Hideki Nakamura, 2011, Journal of dermatological science.

Kindler syndrome with severe intestinal involvement: a 31-year follow-up.

H. Shimizu, Hideki Nakamura, D. Inokuma, 2014, Acta dermato-venereologica.

Collagen XVII deficiency alters epidermal patterning

H. Shimizu, H. Kitahata, K. Natsuga, 2022, Laboratory Investigation.

Epidermolysis bullosa in Japan.

H. Shimizu, K. Natsuga, S. Shinkuma, 2010, Dermatologic clinics.

Refractory Pemphigoid with Autoantibodies to Both BP230 and Laminin gamma1.

T. Hashimoto, Y. Hosokawa, W. Nishie, 2019, Acta dermato-venereologica.

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.

A Cross-Sectional Study Comparing the Prevalence of Bullous Pemphigoid Autoantibodies in 275 Cases of Type II Diabetes Mellitus Treated With or Without Dipeptidyl Peptidase-IV Inhibitors

H. Shimizu, M. Beniko, K. Izumi, 2019, Front. Immunol..

Follicular cyst in a patient with myotonic dystrophy: a case of cyst with differentiation toward follicular infundibulum, isthmus, inner root sheath, and hair.

H. Miyazawa, W. Nishie, M. Iitoyo, 2001, The American Journal of dermatopathology.

Disappearing subcutaneous papules and nodules: Characteristic features of muscle herniation and piezogenic pedal papules

H. Shimizu, W. Nishie, K. Arita, 2017, The Journal of dermatology.

A new clinical variant of acquired reactive perforating dermatosis‐like bullous pemphigoid

H. Shimizu, F. Schauer, L. Bruckner-Tuderman, 2018, The British journal of dermatology.

Lichenoid drug eruption caused by clonazepam

H. Shimizu, K. Natsuga, H. Ujiie, 2017, Journal of the European Academy of Dermatology and Venereology.

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.

Meeting Report of the Pathogenesis of Pemphigus and Pemphigoid Meeting in Munich, September 2016.

H. Koga, H. Shimizu, E. Sprecher, 2017, The Journal of investigative dermatology.

Linear IgA/IgG bullous dermatosis with autoantibodies directing the native and processed forms of BP180

H. Shimizu, K. Natsuga, H. Ujiie, 2020, The British journal of dermatology.

Thymoma‐associated multi‐organ autoimmunity: two cases and a review of the literature

H. Shimizu, T. Nomura, J. Taguchi, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

A novel keratin 5 mutation in an African family with epidermolysis bullosa simplex indicates the importance of the amino acid located at the boundary site between the H1 and coil 1A domains.

M. Akiyama, H. Shimizu, Hideki Nakamura, 2013, Acta dermato-venereologica.

Collagen XVII Processing and Blistering Skin Diseases

W. Nishie, 2020, Acta dermato-venereologica.

Context-Dependent Regulation of Collagen XVII Ectodomain Shedding in Skin.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2015, The American journal of pathology.

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.

Hair follicle stem cell progeny heal blisters while pausing skin development

H. Shimizu, Yasuaki Kobayashi, Hideki Nakamura, 2020, bioRxiv.

Mouse models of autoimmune blistering diseases induced by the passive transfer of antibodies.

W. Nishie, 2013, Methods in molecular biology.

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

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

Bullous pemphigoid developed in a patient with prurigo nodularis

H. Shimizu, K. Izumi, H. Ujiie, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Secondary syphilis mimicking warts in an HIV-positive patient

H. Shimizu, T. Nomura, K. Natsuga, 2009, Sexually Transmitted Infections.

Clinical and immunological characterization of 14 cases of dipeptidyl peptidase‐4 inhibitor‐associated bullous pemphigoid: a single‐centre study

K. Izumi, M. Hayashi, W. Nishie, 2019, The British journal of dermatology.

Disseminated cutaneous Mycobacterium kansasii infection in an patient infected with the human immunodeficiency virus

H. Shimizu, A. Shibaki, W. Nishie, 2009, Clinical and experimental dermatology.

Dipeptidyl peptidase‐4 inhibitor‐associated bullous pemphigoid in a patient with acquired reactive perforating collagenosis

H. Shimizu, K. Izumi, W. Nishie, 2018, Journal of dermatology (Print).

Regression of acquired reactive perforating collagenosis after dipeptidyl peptidase‐4 inhibitor cessation

Y. Matsuno, H. Ujiie, W. Nishie, 2022, The Journal of dermatology.

Dipeptidyl peptidase 4 inhibitor‐associated mucous membrane pemphigoid

H. Koga, T. Dainichi, K. Izumi, 2021, Journal of dermatology (Print).

Immune Reaction to Type XVII Collagen Induces Intramolecular and Intermolecular Epitope Spreading in Experimental Bullous Pemphigoid Models

H. Shimizu, K. Natsuga, H. Ujiie, 2019, Front. Immunol..

Detection of anti‐BP180 NC16A autoantibodies after the onset of dipeptidyl peptidase‐IV inhibitor‐associated bullous pemphigoid: a report of three patients

Masahiko Watanabe, H. Shimizu, T. Nomura, 2018, The British journal of dermatology.

Circumscribed palmar hypokeratosis: correlation between histopathological patterns and dermoscopic findings

H. Shimizu, Y. Fujita, W. Nishie, 2012, The British journal of 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.

Two cases of granular C3 dermatosis with intraepidermal neutrophilic and eosinophilic infiltration possibly induced by anti‐hypertensive drugs

T. Hashimoto, K. Izumi, W. Nishie, 2021, Australasian Journal of Dermatology.

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

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

Wells' syndrome associated with chronic myeloid leukaemia.

H. Shimizu, Y. Fujita, W. Nishie, 2013, Acta dermato-venereologica.

Anti-BP180-type mucous membrane pemphigoid: report of two cases

H. Shimizu, K. Natsuga, Y. Kitagawa, 2014, Odontology.

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.

Dermoscopic observation in adenoma of the nipple

H. Shimizu, T. Nomura, Y. Fujita, 2015, The Journal of dermatology.

Chromosomal inversions as a hidden disease-modifying factor for somatic recombination phenotypes.

M. Akiyama, H. Shimizu, T. Nomura, 2018, JCI insight.

Early severe pachyonychia congenita subtype PC‐K6a with a novel mutation in the KRT6A gene

K. Natsuga, A. Avendaño, W. Nishie, 2017, Journal of the European Academy of Dermatology and Venereology : JEADV.

Update on the pathogenesis of bullous pemphigoid: an autoantibody-mediated blistering disease targeting collagen XVII.

W. Nishie, 2014, Journal of dermatological science.

Detection of a natural antibody targeting the shed ectodomain of BP180 in mice.

K. Izumi, H. Ujiie, W. Nishie, 2023, Journal of dermatological science.

Neonatal Linear IgA Bullous Dermatosis Mediated by Breast Milk-Borne Maternal IgA.

M. Sakamoto, M. Amagai, A. Kubo, 2021, JAMA dermatology.

The direct binding of collagen XVII and collagen IV is disrupted by pemphigoid autoantibodies

H. Shimizu, K. Natsuga, Y. Kitagawa, 2018, Laboratory Investigation.

Noncollagenous 16A domain of type XVII collagen-reactive CD4+ T cells play a pivotal role in the development of active disease in experimental bullous pemphigoid model.

H. Shimizu, A. Shibaki, S. Shinkuma, 2012, Clinical Immunology.

Childhood epidermolysis bullosa acquisita with autoantibodies against the noncollagenous 1 and 2 domains of type VII collagen: case report and review of the literature

W. Nishie, M. Abe, S. Ukae, 2006, The British journal of dermatology.

Mucous membrane pemphigoid with generalized blisters: IgA and IgG autoantibodies target both laminin‐332 and type XVII collagen

H. Shimizu, K. Natsuga, S. Shinkuma, 2012, The British journal of dermatology.

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.

Epitope-Dependent Pathogenicity of Antibodies Targeting a Major Bullous Pemphigoid Autoantigen Collagen XVII/BP180.

H. Shimizu, Hideki Nakamura, K. Natsuga, 2016, The Journal of investigative dermatology.

Intravenous IgG Reduces Pathogenic Autoantibodies, Serum IL-6 Levels, and Disease Severity in Experimental Bullous Pemphigoid Models

K. Natsuga, S. Shinkuma, H. Ujiie, 2019 .

Complement Activation Induce Blister Formation without Bullous Pemphigoid Autoantibodies Directly

H. Shimizu, Hideki Nakamura, K. Natsuga, 2017 .

Dipeptidyl Peptidase-4 Inhibitor-associated Bullous Pemphigoid: Recurrence with Epitope Spreading.

M. Akiyama, H. Shimizu, K. Izumi, 2018, Acta dermato-venereologica.

Case of dipeptidyl peptidase 4 inhibitor‐associated bullous pemphigoid that developed after a scabies infestation

H. Iriki, Katsuya Chinen, M. Yokouchi, 2020, The Journal of dermatology.

Case of bullous pemphigoid accompanied by collagenous gastroenteritis

K. Izumi, W. Nishie, Y. Koike, 2017, The Journal of dermatology.