Hiroshi Shimizu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Hiroshi Shimizu has a total of 214 co-authors. Here are the top co-authors by number of shared publications:
- Yasuyuki Fujita
Department of Dermatology, Asahikawa Medical University , Asahikawa
18 shared publications - Ken Natsuga
Department of Dermatology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University
17 shared publications - Toshifumi Nomura
Department of Dermatology, Institute of Medicine University of Tsukuba Tsukuba Ibaraki Japan
14 shared publications - Riichiro Abe
Division of Dermatology, Niigata University Graduate School of Medical and Dental Sciences
10 shared publications Satoru Shinkuma
Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan; Division of Dermatology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan
9 shared publications- Satoru Shinkuma
Department of Dermatology Nara Medical University Kashihara Japan
9 shared publications
Latest Publications
- 1 April 2021
- Published by Wiley in Journal of the European Academy of Dermatology and Venereology
- Vol. 35 (4) , E282-E285
A case of non-bullous pemphigoid induced by IgG4 autoantibodies targeting BP230
Bullous pemphigoid (BP) is an autoimmune blistering disorder characterized by tense blisters and urticarial erythema. However, more than 20% of patients with BP do not present typical blister formation, but instead present pruritic erythema, a condition called nonbullous pemphigoid (NBP).1,2 The present report is the first to address IgG subclasses of autoantibodies in NBP. We describe a case of NBP with IgG4 autoantibodies alone targeting BP230 but not BP180.
- 1 April 2021
- Published by Wiley in Journal of the European Academy of Dermatology and Venereology
- Vol. 35 (4) , E282-E285
A case of non-bullous pemphigoid induced by IgG4 autoantibodies targeting BP230
Bullous pemphigoid (BP) is an autoimmune blistering disorder characterized by tense blisters and urticarial erythema. However, more than 20% of patients with BP do not present typical blister formation, but instead present pruritic erythema, a condition called nonbullous pemphigoid (NBP).1,2 The present report is the first to address IgG subclasses of autoantibodies in NBP. We describe a case of NBP with IgG4 autoantibodies alone targeting BP230 but not BP180.
- Open Access
- 3 March 2021
- Published by Wiley in Journal of the European Academy of Dermatology and Venereology
- Vol. 35 (8) , E528-E531
Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study
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- 3 March 2021
- Published by Wiley in Journal of the European Academy of Dermatology and Venereology
- Vol. 35 (8) , E528-E531
Open AccessIntravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study
Click on the article title to read more.
- 1 January 2021
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 141 (1) , 198-202.e6
Intravenous Injection of Muse Cells as a Potential Therapeutic Approach for Epidermolysis Bullosa
- 1 January 2021
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 141 (1) , 198-202.e6
Intravenous Injection of Muse Cells as a Potential Therapeutic Approach for Epidermolysis Bullosa
- 24 September 2020
- Published by Wiley in International Journal of Dermatology
- Vol. 60 (3) , E92-E94
A case of mucous membrane pemphigoid with anti‐BP230 autoantibodies alone
- 24 September 2020
- Published by Wiley in International Journal of Dermatology
- Vol. 60 (3) , E92-E94
A case of mucous membrane pemphigoid with anti‐BP230 autoantibodies alone
- 1 August 2020
- Published by Elsevier in Journal of Dermatological Science
- Vol. 99 (2) , 109-118
Loss of dynamin-related protein 1 (Drp1) does not affect epidermal development or UVB-induced apoptosis but does accelerate UVB-induced carcinogenesis
- 1 August 2020
- Published by Elsevier in Journal of Dermatological Science
- Vol. 99 (2) , 109-118
Loss of dynamin-related protein 1 (Drp1) does not affect epidermal development or UVB-induced apoptosis but does accelerate UVB-induced carcinogenesis
- 6 April 2020
- Published by Wiley in Journal of the European Academy of Dermatology and Venereology
- Vol. 34 (9) , E510-E513
Drp1 expression levels correlate with clinical stage in extramammary Paget’s disease
Extramammary Paget’s disease (EMPD) is a rare malignant neoplasm that often presents in areas that abound in apocrine sweat glands1. Dynamin related protein 1 (Drp1) is a GTPase that regulates mitochondrial fission2. Recently, several studies have reported that Drp1 plays critical roles in malignant neoplasms3, 4. However, little is known about the Drp1 function in EMPD. Further, mTOR is reported to be associated with malignancy in EMPD5. In this study, we investigate Drp1 and mTOR expression levels in EMPD through immunochemical analyses of clinical samples and analyzed the correlation between the expression levels of Drp1 or mTOR and the clinical information. We found a positive correlation between the expression levels of Drp1 or mTOR and clinical stage of EMPD.
- 6 April 2020
- Published by Wiley in Journal of the European Academy of Dermatology and Venereology
- Vol. 34 (9) , E510-E513
Drp1 expression levels correlate with clinical stage in extramammary Paget’s disease
Extramammary Paget’s disease (EMPD) is a rare malignant neoplasm that often presents in areas that abound in apocrine sweat glands1. Dynamin related protein 1 (Drp1) is a GTPase that regulates mitochondrial fission2. Recently, several studies have reported that Drp1 plays critical roles in malignant neoplasms3, 4. However, little is known about the Drp1 function in EMPD. Further, mTOR is reported to be associated with malignancy in EMPD5. In this study, we investigate Drp1 and mTOR expression levels in EMPD through immunochemical analyses of clinical samples and analyzed the correlation between the expression levels of Drp1 or mTOR and the clinical information. We found a positive correlation between the expression levels of Drp1 or mTOR and clinical stage of EMPD.
- 1 October 2019
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 139 (10) , 2115-2124.e11
Cultured Epidermal Autografts from Clinically Revertant Skin as a Potential Wound Treatment for Recessive Dystrophic Epidermolysis Bullosa
- 1 October 2019
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 139 (10) , 2115-2124.e11
Cultured Epidermal Autografts from Clinically Revertant Skin as a Potential Wound Treatment for Recessive Dystrophic Epidermolysis Bullosa
- Open Access
- 28 August 2019
- Published by Morressier GmbH
The impact of Fc-binding proteins on IgG targeting BP180
Immunoglobulins consist of two antigen-binding F(ab’)2 variable regions and one constant (Fc) region. Several proteins have the ability to bind to the Fc region, e.g. Fc-receptors, complement C1q, protein A and rheumatoid factor (RF). It is well known that some Fc-binding proteins, including complement C1q and rheumatoid factor, are physiologically present in the body. Regarding
- 28 August 2019
- Published by Morressier GmbH
Open AccessThe impact of Fc-binding proteins on IgG targeting BP180
Immunoglobulins consist of two antigen-binding F(ab’)2 variable regions and one constant (Fc) region. Several proteins have the ability to bind to the Fc region, e.g. Fc-receptors, complement C1q, protein A and rheumatoid factor (RF). It is well known that some Fc-binding proteins, including complement C1q and rheumatoid factor, are physiologically present in the body. Regarding
- 1 August 2019
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 139 (8) , 1711-1721.e4
Efficient Gene Reframing Therapy for Recessive Dystrophic Epidermolysis Bullosa with CRISPR/Cas9
- 1 August 2019
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 139 (8) , 1711-1721.e4
Efficient Gene Reframing Therapy for Recessive Dystrophic Epidermolysis Bullosa with CRISPR/Cas9
- Open Access
- 1 December 2018
- Published by Elsevier in Environment International
- Vol. 121, 102-110
Association of filaggrin gene mutations and childhood eczema and wheeze with phthalates and phosphorus flame retardants in house dust: The Hokkaido study on Environment and Children's Health
- 1 December 2018
- Published by Elsevier in Environment International
- Vol. 121, 102-110
Open AccessAssociation of filaggrin gene mutations and childhood eczema and wheeze with phthalates and phosphorus flame retardants in house dust: The Hokkaido study on Environment and Children's Health