Hiroshi Shimizu
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Researcher ORCID 0000-0002-9930-1326
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Hiroshi Shimizu's Degrees
- PhD Computer Science University of Tokyo
- Masters Computer Science University of Tokyo
- Bachelors Computer Science University of Tokyo
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(Suggest an Edit or Addition)Hiroshi Shimizu's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB. (2008) (858)
- Inherited epidermolysis bullosa: updated recommendations on diagnosis and classification. (2014) (762)
- Mesenchymal Stem Cells Are Recruited into Wounded Skin and Contribute to Wound Repair by Transdifferentiation into Multiple Skin Cell Type1 (2008) (725)
- Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009. (2010) (644)
- Consensus statement on definitions of disease, end points, and therapeutic response for pemphigus. (2008) (465)
- Revised classification system for inherited epidermolysis bullosa: Report of the Second International Consensus Meeting on diagnosis and classification of epidermolysis bullosa. (2000) (417)
- Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer. (2005) (362)
- Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome. (2003) (337)
- Definitions and outcome measures for bullous pemphigoid: recommendations by an international panel of experts. (2012) (274)
- Toxic epidermal necrolysis and Stevens-Johnson syndrome are induced by soluble Fas ligand. (2003) (260)
- Unique mutations in the filaggrin gene in Japanese patients with ichthyosis vulgaris and atopic dermatitis. (2007) (228)
- A novel subepidermal blistering disease with autoantibodies to a 200-kDa antigen of the basement membrane zone. (1996) (217)
- A randomized double-blind trial of intravenous immunoglobulin for pemphigus. (2009) (209)
- Diagnosis and Management of Pemphigus: recommendations by an International Panel of Experts. (2018) (197)
- Autoantibody Profile Differentiates between Inflammatory and Noninflammatory Bullous Pemphigoid. (2016) (186)
- Clinical severity correlates with impaired barrier in filaggrin-related eczema. (2009) (167)
- Lupus erythematosus panniculitis (lupus profundus): Clinical, histopathological, and molecular analysis of nine cases (2005) (159)
- Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy. (1996) (159)
- Humanization of autoantigen (2007) (153)
- Production of rabbit antibodies against carboxy-terminal epitopes encoded by bullous pemphigoid cDNA. (1990) (152)
- Regulation of human melanoma growth and metastasis by AGE-AGE receptor interactions. (2004) (146)
- Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan. (2008) (135)
- Impaired Epidermal Permeability Barrier in Mice Lacking Elovl1, the Gene Responsible for Very-Long-Chain Fatty Acid Production (2013) (133)
- Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation. (2003) (131)
- Overexpression of pigment epithelium-derived factor decreases angiogenesis and inhibits the growth of human malignant melanoma cells in vivo. (2004) (129)
- Epidermal basement membrane zone components: ultrastructural distribution and molecular interactions. (2003) (127)
- Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan. (2004) (124)
- The extracellular domain of BPAG2 localizes to anchoring filaments and its carboxyl terminus extends to the lamina densa of normal human epidermal basement membrane. (1997) (110)
- Oncostatin M receptor-beta mutations underlie familial primary localized cutaneous amyloidosis. (2008) (106)
- Dietary glucosylceramide improves skin barrier function in hairless mice. (2006) (105)
- PDGF isoforms induce and maintain anagen phase of murine hair follicles. (2006) (105)
- Correlation of clinical severity and ELISA indices for the NC16A domain of BP180 measured using BP180 ELISA kit in bullous pemphigoid. (2005) (105)
- Distinct behavior of human Langerhans cells and inflammatory dendritic epidermal cells at tight junctions in patients with atopic dermatitis. (2014) (101)
- Kikuchi's disease and the skin: case report and review of the literature (2001) (100)
- Granulysin as a marker for early diagnosis of the Stevens-Johnson syndrome. (2009) (99)
- Filaggrin gene defects and the risk of developing allergic disorders. (2011) (96)
- CTACK/CCL27 Accelerates Skin Regeneration via Accumulation of Bone Marrow‐Derived Keratinocytes (2006) (96)
- The clinical spectrum of nonbullous congenital ichthyosiform erythroderma and lamellar ichthyosis (2003) (93)
- Coexistence of psoriasis and an unusual IgG‐mediated subepidermal bullous dermatosis: identification of a novel 200‐kDa lower lamina lucida target antigen (1996) (93)
- A case of linear IgA buUous dermatosis with IgA anti‐type VII collagen autoantibodies (1996) (92)
- Clinical histopathological characteristics of basal cell carcinoma in Japanese patients. (1996) (92)
- Sequential reorganization of cornified cell keratin filaments involving filaggrin-mediated compaction and keratin 1 deimination. (2002) (92)
- An update on molecular aspects of the non‐syndromic ichthyoses (2008) (91)
- Paper-based ELISA for the detection of autoimmune antibodies in body fluid-the case of bullous pemphigoid. (2014) (90)
- Epidermolysis bullosa simplex associated with pyloric atresia is a novel clinical subtype caused by mutations in the plectin gene (PLEC1). (2005) (87)
- Ultraviolet A-induced Production of Matrix Metalloproteinase-1 Is Mediated by Macrophage Migration Inhibitory Factor (MIF) in Human Dermal Fibroblasts* (2004) (87)
- A group of atopic dermatitis without IgE elevation or barrier impairment shows a high Th1 frequency: possible immunological state of the intrinsic type. (2012) (86)
- Truncation of CGI-58 protein causes malformation of lamellar granules resulting in ichthyosis in Dorfman-Chanarin syndrome. (2003) (86)
- Pemphigus vulgaris and pemphigus foliaceus sera show an inversely graded binding pattern to extracellular regions of desmosomes in different layers of human epidermis. (1995) (86)
- Bullous Pemphigoid Autoantibodies Directly Induce Blister Formation without Complement Activation (2014) (85)
- An annexin A1–FPR1 interaction contributes to necroptosis of keratinocytes in severe cutaneous adverse drug reactions (2014) (83)
- Autoantibodies from patients with cicatricial pemphigoid target different sites in epidermal basement membrane. (1995) (83)
- Mutation analysis of the ADAR1 gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis. (2005) (82)
- Development of pemphigus vulgaris in a patient with pemphigus foliaceus: antidesmoglein antibody profile shift confirmed by enzyme-linked immunosorbent assay. (2000) (82)
- Novel duplication mutation in the patatin domain of adipose triglyceride lipase (PNPLA2) in neutral lipid storage disease with severe myopathy (2007) (82)
- Molecular basis of recessive dystrophic epidermolysis bullosa: genotype/phenotype correlation in a case of moderate clinical severity. (1996) (81)
- Fibroblasts show more potential as target cells than keratinocytes in COL7A1 gene therapy of dystrophic epidermolysis bullosa. (2006) (80)
- Changing patterns of localization of putative stem cells in developing human hair follicles. (2000) (80)
- Macrophage Migration Inhibitory Factor Is Induced by Thrombin and Factor Xa in Endothelial Cells* (2004) (80)
- 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. (2006) (79)
- Delayed assembly of desmosomes in keratinocytes with disrupted classic-cadherin-mediated cell adhesion by a dominant negative mutant. (1995) (79)
- A denatured collagen microfiber scaffold seeded with human fibroblasts and keratinocytes for skin grafting. (2011) (76)
- Most anchoring fibrils in human skin originate and terminate in the lamina densa. (1997) (76)
- Type XVII collagen coordinates proliferation in the interfollicular epidermis (2017) (75)
- HLA-DQB1*03:01 as a Biomarker for Genetic Susceptibility to Bullous Pemphigoid Induced by DPP-4 Inhibitors. (2017) (74)
- Harlequin ichthyosis model mouse reveals alveolar collapse and severe fetal skin barrier defects. (2008) (74)
- Increased soluble Fas ligand levels in patients with Stevens-Johnson syndrome and toxic epidermal necrolysis preceding skin detachment. (2008) (74)
- 97-kDa linear IgA bullous dermatosis (LAD) antigen localizes to the lamina lucida of the epidermal basement membrane. (1996) (73)
- Dissociation of intra‐ and extracellular domainsof desmosomal cadherins and E‐cadherin inHailey–Hailey disease and Darier’s disease (2000) (73)
- FLG mutation p.Lys4021X in the C‐terminal imperfect filaggrin repeat in Japanese patients with atopic eczema (2009) (72)
- Minodronate, a newly developed nitrogen-containing bisphosphonate, suppresses melanoma growth and improves survival in nude mice by blocking vascular endothelial growth factor signaling. (2004) (71)
- Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa. (1997) (70)
- Localization of ABCA12 from Golgi apparatus to lamellar granules in human upper epidermal keratinocytes (2007) (70)
- Rapid immunochromatographic test for serum granulysin is useful for the prediction of Stevens-Johnson syndrome and toxic epidermal necrolysis. (2011) (70)
- Protective effects of platinum nanoparticles against UV‐light‐induced epidermal inflammation (2010) (70)
- Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma (2012) (69)
- Periderm cells form cornified cell envelope in their regression process during human epidermal development. (1999) (68)
- Antibodies to Pathogenic Epitopes on Type XVII Collagen Cause Skin Fragility in a Complement-Dependent and -Independent Manner (2012) (66)
- Alterations in desmosome size and number coincide with the loss of keratinocyte cohesion in skin with homozygous and heterozygous defects in the desmosomal protein plakophilin 1. (2003) (64)
- Desmosomes: Structure and Function in Normal and Diseased Epidermis (2001) (64)
- Bone marrow transplantation restores epidermal basement membrane protein expression and rescues epidermolysis bullosa model mice (2010) (63)
- High macrophage migration inhibitory factor (MIF) serum levels associated with extended psoriasis. (2001) (63)
- Transformation‐specific matrix metalloproteinases (MMP)‐7 and MMP‐13 are expressed by tumour cells in epidermolysis bullosa‐associated squamous cell carcinomas (2008) (62)
- Epidermolysis bullosa acquisita antigen and the carboxy terminus of type VII collagen have a common immunolocalization to anchoring fibrils and lamina densa of basement membrane (1990) (61)
- Solitary cutaneous malignant schwannoma. Immunohistochemical and ultrastructural studies. (1993) (61)
- White fibrous papulosis of the neck: a new clinicopathologic entity? (1989) (61)
- A novel variant of acquired epidermolysis bullosa with autoantibodies against the central triple-helical domain of type VII collagen. (1997) (61)
- Epidermolysis bullosa simplex associated with muscular dystrophy: phenotype-genotype correlations and review of the literature. (1999) (60)
- Type XVII collagen is a key player in tooth enamel formation. (2009) (60)
- Pityriasis Rubra Pilaris Type V as an Autoinflammatory Disease by CARD14 Mutations (2017) (59)
- Induction of therapeutically relevant cytotoxic T lymphocytes in humans by percutaneous peptide immunization. (2006) (58)
- Human IgG1 Monoclonal Antibody against Human Collagen 17 Noncollagenous 16A Domain Induces Blisters via Complement Activation in Experimental Bullous Pemphigoid Model (2010) (58)
- Autoantibodies in anti‐p200 pemphigoid stain skin lacking laminin 5 and type VII collagen (2000) (55)
- Prevalent LIPH founder mutations lead to loss of P2Y5 activation ability of PA‐PLA1α in autosomal recessive hypotrichosis (2010) (55)
- Regulatory T‐cell dysfunction induces autoantibodies to bullous pemphigoid antigens in mice and human subjects (2018) (54)
- A Novel Active Mouse Model for Bullous Pemphigoid Targeting Humanized Pathogenic Antigen (2010) (54)
- Expression of RNA-binding protein Musashi in hair follicle development and hair cycle progression. (2006) (54)
- Zinc dental fillings and palmoplantar pustulosis (2005) (54)
- The use of silver-enhanced 1-nm gold probes for light and electron microscopic localization of intra- and extracellular antigens in skin. (1992) (54)
- Novel ITGB4 mutations in a patient with junctional epidermolysis bullosa-pyloric atresia syndrome and altered basement membrane zone immunofluorescence for the alpha6beta4 integrin. (1997) (53)
- Neutral lipid storage leads to acylceramide deficiency, likely contributing to the pathogenesis of Dorfman-Chanarin syndrome. (2010) (53)
- Prenatal Diagnosis for Recessive Dystrophic Epidermolysis Bullosa in 10 Families by Mutation and Haplotype Analysis in the Type VII Collagen Gene (COL7A1) (1996) (53)
- Beta defensin-3 engineered epidermis shows highly protective effect for bacterial infection (2005) (52)
- In vivo analysis of IgE autoantibodies in bullous pemphigoid: a study of 100 cases. (2015) (52)
- DNA-based prenatal diagnosis of harlequin ichthyosis and characterization of ABCA12 mutation consequences. (2007) (52)
- Comprehensive screening for a complete set of Japanese‐population‐specific filaggrin gene mutations (2014) (51)
- Successful treatment of severe recalcitrant erosive oral lichen planus with topical tacrolimus (2006) (51)
- What’s new in bullous pemphigoid (2010) (51)
- The role of PEDF in tumor growth and metastasis. (2010) (50)
- Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis. (2009) (50)
- Plectin defects in epidermolysis bullosa simplex with muscular dystrophy (2007) (50)
- Self-improvement of keratinocyte differentiation defects during skin maturation in ABCA12-deficient harlequin ichthyosis model mice. (2010) (49)
- Complete Paternal Uniparental Isodisomy of Chromosome 1: A Novel Mechanism for Herlitz Junctional Epidermolysis Bullosa (2000) (49)
- Compound heterozygous mutations including a de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity. (2006) (49)
- Childhood epidermolysis bullosa acquisita with autoantibodies against the noncollagenous 1 and 2 domains of type VII collagen: case report and review of the literature (2006) (49)
- Embryonic hair follicle fate change by augmented β-catenin through Shh and Bmp signaling (2009) (48)
- Plectin Deficiency Leads to Both Muscular Dystrophy and Pyloric Atresia in Epidermolysis Bullosa Simplex (2010) (48)
- Novel ABCA12 mutations identified in two cases of non-bullous congenital ichthyosiform erythroderma associated with multiple skin malignant neoplasia. (2007) (48)
- Lupus erythematosus profundus successfully treated with dapsone: review of the literature. (2006) (48)
- Tissue regeneration using macrophage migration inhibitory factor-impregnated gelatin microbeads in cutaneous wounds. (2005) (48)
- Is tubular apocrine adenoma a distinct clinical entity? (1993) (47)
- Demonstration of intra- and extracellular localization of bullous pemphigoid antigen using cryofixation and freeze substitution for postembedding immunoelectron microscopy (2004) (47)
- Japanese-specific filaggrin gene mutations in Japanese patients suffering from atopic eczema and asthma. (2010) (46)
- Small-diameter porous poly (epsilon-caprolactone) films enhance adhesion and growth of human cultured epidermal keratinocyte and dermal fibroblast cells. (2007) (46)
- Interleukin-1beta and macrophage migration inhibitory factor (MIF) in dermal fibroblasts mediate UVA-induced matrix metalloproteinase-1 expression. (2008) (45)
- A homozygous missense mutation in the cytoplasmic tail of beta4 integrin, G931D, that disrupts hemidesmosome assembly and underlies Non-Herlitz junctional epidermolysis bullosa without pyloric atresia? (2000) (45)
- Dipeptidyl peptidase‐4 inhibitors‐associated bullous pemphigoid: A retrospective study of 168 pemphigoid and 9,304 diabetes mellitus patients (2018) (45)
- Dermatitis herpetiformis in Japan: An Update (2002) (45)
- High expression of Ki-67 and cyclin D1 in invasive extramammary Paget's disease. (2008) (45)
- Dominant and Recessive Compound Heterozygous Mutations in Epidermolysis Bullosa Simplex Demonstrate the Role of the Stutter Region in Keratin Intermediate Filament Assembly* (2002) (45)
- A novel splice site mutation in NCSTN underlies a Japanese family with hidradenitis suppurativa (2013) (44)
- Mutational analysis of the ATP2A2 gene in two Darier disease families with intrafamilial variability (2004) (44)
- Oculocutaneous albinism type 4: six novel mutations in the membrane-associated transporter protein gene and their phenotypes. (2006) (44)
- Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations (2009) (44)
- Unique clinical and serological features of bullous pemphigoid associated with dipeptidyl peptidase‐4 inhibitors (2018) (44)
- Malignant skin tumours in patients with inherited ichthyosis (2011) (44)
- Presence of Circulating CCR10+ T cells and Elevated Serum CTACK/CCL27 in the Early Stage of Mycosis Fungoides (2006) (43)
- Usefulness of real‐time tissue elastography for detecting lymph‐node metastases in squamous cell carcinoma (2009) (43)
- Compound heterozygosity for silent and dominant glycine substitution mutations in COL7A1 leads to a marked transient intracytoplasmic retention of procollagen VII and a moderately severe dystrophic epidermolysis bullosa phenotype. (1999) (43)
- Regional difference in expression of characteristic abnormality of harlequin ichthyosis in affected fetuses (1998) (43)
- Novel mutations of TGM1 in a child with congenital ichthyosiform erythroderma (2001) (43)
- Desmoyokin/AHNAK protein localizes to the non-desmosomal keratinocyte cell surface of human epidermis. (1995) (43)
- 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. (1999) (42)
- Pyoderma gangrenosum associated with Takayasu's arteritis (2004) (42)
- Blockade of autoantibody-initiated tissue damage by using recombinant fab antibody fragments against pathogenic autoantigen. (2010) (42)
- Stratum corneum hydration and flexibility are useful parameters to indicate clinical severity of congenital ichthyosis (2005) (42)
- Changes in Gap Junction Distribution and Connexin Expression Pattern During Human Fetal Skin Development (2002) (42)
- Keratin 1 gene mutation detected in epidermal nevus with epidermolytic hyperkeratosis. (2007) (42)
- The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa. (2004) (41)
- Hidradenoma papilliferum with mixed histopathologic features of syringocystadenoma papilliferum and anogenital mammary‐like glands (2004) (41)
- Expression of transglutaminase activity in developing human epidermis (2000) (41)
- 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. (2006) (40)
- Human bullous pemphigoid antigen 2 transgenic skin elicits specific IgG in wild-type mice. (2007) (40)
- Ultrastructure and molecular pathogenesis of epidermolysis bullosa. (2011) (39)
- Plectin expression patterns determine two distinct subtypes of epidermolysis bullosa simplex (2010) (39)
- Ichthyosis bullosa of Siemens: its correct diagnosis facilitated by molecular genetic testing (2005) (39)
- Glycine substitution mutations by different amino acids in the same codon of COL7A1 lead to heterogeneous clinical phenotypes of dominant dystrophic epidermolysis bullosa (2000) (39)
- Elephantiasis Nostras Verrucosa Successfully Treated by Surgical Debridement (2004) (39)
- Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa (2005) (39)
- Ultrastructural Orientation of Laminin 5 in the Epidermal Basement Membrane: an Updated Model for Basement Membrane Organization 1 (2003) (39)
- Circulating IgA and IgE autoantibodies in antilaminin‐332 mucous membrane pemphigoid (2010) (39)
- Maternal uniparental meroisodisomy in the LAMB3 region of chromosome 1 results in lethal junctional epidermolysis bullosa. (1998) (38)
- Is cutaneous plasmacytosis a distinct clinical entity? (1997) (38)
- The extracellular domain of BPAG2 has a loop structure in the carboxy terminal flexible tail in vivo. (2000) (38)
- Second harmonic generation and multiphoton microscopic detection of collagen without the need for species specific antibodies. (2011) (37)
- Expression of the keratinocyte lipid transporter ABCA12 in developing and reconstituted human epidermis. (2007) (37)
- Bullous Pemphigoid Triggered by Thermal Burn Under Medication With a Dipeptidyl Peptidase-IV Inhibitor: A Case Report and Review of the Literature (2018) (37)
- Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism. (2004) (37)
- Four novel plectin gene mutations in Japanese patients with epidermolysis bullosa with muscular dystrophy disclosed by heteroduplex scanning and protein truncation tests. (1999) (36)
- A case of interstitial granulomatous drug reaction due to sennoside (2004) (36)
- Promoter region polymorphism of macrophage migration inhibitory factor is strong risk factor for young onset of extensive alopecia areata (2005) (36)
- Changing pattern of deiminated proteins in developing human epidermis. (2003) (36)
- Nail dystrophy and blisters as sole manifestations in myeloma-associated amyloidosis. (2006) (36)
- Epidermolysis bullosa simplex in Japanese and Korean patients: genetic studies in 19 cases (2006) (36)
- 97 kDa linear IgA bullous dermatosis antigen localizes in the lamina lucida between the NC16A and carboxyl terminal domains of the 180 kDa bullous pemphigoid antigen. (1998) (36)
- A comparative immunoelectron microscopic study of typical and atypical cases of pemphigoid (1988) (35)
- Granulomatous arteritis in cutaneous lesions of Churg–Strauss syndrome (2007) (35)
- Expression and ultrastructural localization of HMB‐45 antigen (1996) (35)
- Analysis of ATP2C1 gene mutation in 10 unrelated Japanese families with Hailey-Hailey disease. (2002) (35)
- Abca12-mediated lipid transport and Snap29-dependent trafficking of lamellar granules are crucial for epidermal morphogenesis in a zebrafish model of ichthyosis (2011) (35)
- Differences in recurrent COL7A1 mutations in dystrophic epidermolysis bullosa: ethnic-specific and worldwide recurrent mutations (2004) (35)
- Pemphigus: from immunofluorescence to molecular biology. (1996) (34)
- Absence of detectable alpha 6 integrin in pyloric atresia-junctional epidermolysis bullosa syndrome. Application for prenatal diagnosis in a family at risk for recurrence. (1996) (34)
- Identification of the hemidesmosomal 500 kDa protein (HD1) as plectin. (1999) (34)
- Clinical and serological transition from pemphigus vulgaris to pemphigus foliaceus demonstrated by desmoglein ELISA system. (2002) (34)
- Efficient Gene Reframing Therapy for Recessive Dystrophic Epidermolysis Bullosa with CRISPR/Cas9. (2019) (34)
- A novel subepidermal blistering disease with autoantibodies to a 200-kDa antigen of the basement membrane zone. (1996) (34)
- Japanese guidelines for the management of pemphigoid (including epidermolysis bullosa acquisita) (2019) (34)
- Granzyme B inhibition reduces disease severity in autoimmune blistering diseases (2021) (34)
- The South African "bathing suit ichthyosis" is a form of lamellar ichthyosis caused by a homozygous missense mutation, p.R315L, in transglutaminase 1. (2007) (33)
- A Novel Humanized Neonatal Autoimmune Blistering Skin Disease Model Induced by Maternally Transferred Antibodies1 (2009) (33)
- Toenail dystrophy with COL7A1 glycine substitution mutations segregates as an autosomal dominant trait in 2 families with dystrophic epidermolysis bullosa. (2002) (33)
- Meeting Report of the Pathogenesis of Pemphigus and Pemphigoid Meeting in Munich, September 2016. (2017) (33)
- Life before and beyond blistering: The role of collagen XVII in epidermal physiology (2018) (33)
- Collagen XVII participates in keratinocyte adhesion to collagen IV, and in p38MAPK-dependent migration and cell signaling. (2009) (33)
- Clinical approaches toward tumor angiogenesis: past, present and future. (2008) (33)
- Clinical heterogeneity of 1649delG mutation in the tail domain of keratin 5: a Japanese family with epidermolysis bullosa simplex with mottled pigmentation. (2005) (32)
- Successful treatment of nail lichen planus with topical tacrolimus. (2010) (32)
- Subcutaneous nodules on the buttocks as a manifestation of dialysis‐related amyloidosis: a clinicopathological entity? (2003) (32)
- Squamous cell carcinoma developing in a 12‐year‐old boy with nonHallopeau–Siemens recessive dystrophic epidermolysis bullosa (2003) (32)
- Topical application of anti-angiogenic peptides based on pigment epithelium-derived factor can improve psoriasis. (2010) (31)
- Prenatal diagnosis of harlequin ichthyosis by the examination of keratinized hair canals and amniotic fluid cells at 19 weeks' estimated gestational age (1999) (31)
- Macrophage migration inhibitory factor is essential for eosinophil recruitment in allergen-induced skin inflammation. (2011) (31)
- Impaired contact hypersensitivity in macrophage migration inhibitory factor‐deficient mice (2003) (31)
- Novel ALDH3A2 heterozygous mutations are associated with defective lamellar granule formation in a Japanese family of Sjögren-Larsson syndrome. (2004) (31)
- A novel NCSTN mutation alone may be insufficient for the development of familial hidradenitis suppurativa. (2014) (31)
- ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma. (2009) (31)
- Highly prevalent SERPINB7 founder mutation causes pseudodominant inheritance pattern in Nagashima‐type palmoplantar keratosis (2014) (30)
- Epitope-Dependent Pathogenicity of Antibodies Targeting a Major Bullous Pemphigoid Autoantigen Collagen XVII/BP180. (2016) (30)
- Six novel P gene mutations and oculocutaneous albinism type 2 frequency in Japanese albino patients. (2003) (30)
- Development of lichen planus and psoriasis on lesions of vitiligo vulgaris (2006) (30)
- Linagliptin‐associated bullous pemphigoid that was most likely caused by IgG autoantibodies against the midportion of BP180 (2017) (29)
- Mutation report: complete paternal uniparental isodisomy of chromosome 1: a novel mechanism for Herlitz junctional epidermolysis bullosa. (2000) (29)
- The majority of keratinocytes incorporate intradermally injected plasmid DNA regardless of size but only a small proportion of cells can express the gene product. (2002) (29)
- Epidermal triglyceride levels are correlated with severity of ichthyosis in Dorfman-Chanarin syndrome. (2010) (29)
- Formation of cornified cell envelope in human hair follicle development (2002) (29)
- Drp1 regulates mitochondrial morphology and cell proliferation in cutaneous squamous cell carcinoma. (2017) (29)
- Malignant epithelioid schwannoma of the skin showing partial HMB-45 positivity. (1993) (29)
- CGI-58 is an alpha/beta-hydrolase within lipid transporting lamellar granules of differentiated keratinocytes. (2008) (29)
- Immunological Reconstitution after Autologous Hematopoietic Stem Cell Transplantation in Patients with Systemic Sclerosis: Relationship Between Clinical Benefits and Intensity of Immunosuppression (2009) (29)
- A case of bullous pemphigoid with antidesmoplakin autoantibodies (1994) (29)
- Revertant Mosaicism in Ichthyosis with Confetti Caused by a Frameshift Mutation in KRT1. (2016) (28)
- Characterization of Kdap, a protein secreted by keratinocytes. (2004) (28)
- Two cases of atypical membranous aplasia cutis with hair collar sign: one with dermal melanocytosis, and the other with naevus flammeus (2005) (28)
- ABCA12 dysfunction causes a disorder in glucosylceramide accumulation during keratinocyte differentiation. (2010) (28)
- The 97 kDa linear IgA bullous dermatosis antigen is not expressed in a patient with generalized atrophic benign epidermolysis bullosa with a novel homozygous G258X mutation in COL17A1. (1998) (28)
- Prenatal exclusion of harlequin ichthyosis; potential pitfalls in the timing of the fetal skin biopsy (2005) (27)
- Response of intractable skin ulcers in recessive dystrophic epidermolysis bullosa patients to an allogeneic cultured dermal substitute. (2010) (27)
- Development of bullous pemphigoid during treatment of psoriatic onycho‐pachydermo periostitis with ustekinumab (2015) (27)
- Detection of 1733insC mutations in an Asian family with Birt–Hogg–Dubé syndrome (2005) (27)
- Filaggrin Mutation in Korean Patients with Atopic Dermatitis (2017) (27)
- Extracellular cleavage of collagen XVII is essential for correct cutaneous basement membrane formation. (2016) (27)
- The development of induced pluripotent stem cell-derived mesenchymal stem/stromal cells from normal human and RDEB epidermal keratinocytes. (2018) (27)
- Compound heterozygous TGM1 mutations including a novel missense mutation L204Q in a mild form of lamellar ichthyosis. (2001) (27)
- Upregulation of P‐cadherin expression in the lesional skin of pemphigus, Hailey‐Hailey disease and Darier’s disease (2001) (26)
- Bacterial infection‐induced generalized Hailey–Hailey disease successfully treated by etretinate (2006) (26)
- Prolonged elevation of serum granulysin in drug‐induced hypersensitivity syndrome (2012) (26)
- Stevens-Johnson syndrome/toxic epidermal necrolysis mouse model generated by using PBMCs and the skin of patients. (2013) (26)
- Loss of TRIM29 Alters Keratin Distribution to Promote Cell Invasion in Squamous Cell Carcinoma. (2018) (26)
- New insights into the immunoultrastructural organization of cutaneous basement membrane zone molecules (1998) (26)
- Extensive proliferative nodules in a case of giant congenital naevus (2008) (26)
- Keratinocyte-/fibroblast-targeted rescue of Col7a1-disrupted mice and generation of an exact dystrophic epidermolysis bullosa model using a human COL7A1 mutation. (2009) (26)
- Establishment of a novel experimental model of human angiosarcoma and a VEGF-targeting therapeutic experiment. (2013) (26)
- Spontaneous giant aneurysm of the superficial temporal artery: case report. (2009) (26)
- Gentamicin-Induced Readthrough and Nonsense-Mediated mRNA Decay of SERPINB7 Nonsense Mutant Transcripts. (2017) (25)
- Cetirizine, an H1‐receptor antagonist, suppresses the expression of macrophage migration inhibitory factor: its potential anti‐inflammatory action (2004) (25)
- 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. (2012) (25)
- A case of drug-associated dermatomyositis following ipilimumab therapy (2016) (25)
- Deficient deletion of apoptotic cells by macrophage migration inhibitory factor (MIF) overexpression accelerates photocarcinogenesis. (2009) (25)
- Prenatal diagnosis as a test for genodermatoses: its past, present and future. (1999) (25)
- Staging and Assessment of Lymph Node Involvement by18F‐Fluorodeoxyglucose–Positron Emission Tomography in Invasive Extramammary Paget's Disease (2005) (25)
- 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. (2018) (25)
- Detection of anti‐BP180 NC16A autoantibodies after the onset of dipeptidyl peptidase‐IV inhibitor‐associated bullous pemphigoid: a report of three patients (2018) (25)
- Pathogenesis of bullous pemphigoid. (2012) (25)
- Isolated adrenocorticotropic hormone deficiency associated with nivolumab therapy (2017) (24)
- Novel mutations in the LAMB3 gene shared by two Japanese unrelated families with Herlitz junctional epidermolysis bullosa, and their application for prenatal testing. (1998) (24)
- Demonstration of desmosomal antigens by electron microscopy using cryofixed and cryosubstituted skin with silver-enhanced gold probe. (1994) (24)
- Epidermolysis bullosa acquisita associated with psoriasis vulgaris (2007) (24)
- Animal models of epidermolysis bullosa. (2010) (24)
- Follicular mucinosis associated with imatinib (STI571) (2004) (24)
- Prenatal exclusion of pyloric atresia-junctional epidermolysis bullosa syndrome. (1994) (24)
- Epithelioid sarcoma presenting as pulmonary cysts with cancer antigen 125 expression (2006) (24)
- Cornified cell envelope proteins and keratins are normally distributed in harlequin ichthyosis (1996) (24)
- Autoantibodies to Multiple Epitopes on the Non-Collagenous-1 Domain of Type VII Collagen Induce Blisters. (2015) (24)
- Deficient stratum corneum intercellular lipid in a Japanese patient with lamellar ichthyosis with a homozygous deletion mutation in SDR9C7 (2017) (24)
- Expression of c-maf and mafB genes in the skin during rat embryonic development. (2004) (23)
- CADM1 is a diagnostic marker in early‐stage mycosis fungoides: Multicenter study of 58 cases (2018) (23)
- Hair follicle stem cell-targeted gene transfer and reconstitution system (2006) (23)
- Exclusion of COL7A1 mutation in Kindler syndrome. (2002) (23)
- Direct injection of plasmid DNA into the skin induces dermatitis by activation of monocytes through toll‐like receptor 9 (2005) (23)
- Mild recessive bullous congenital ichthyosiform erythroderma due to a previously unidentified homozygous keratin 10 nonsense mutation. (2008) (23)
- CD8+ cutaneous anaplastic large‐cell lymphoma: report of two cases with immunophenotyping, T‐cell‐receptor gene rearrangement and electron microscopic studies (1992) (23)
- Prenatal diagnosis of oculocutaneous albinism by analysis of the fetal tyrosinase gene. (1994) (23)
- Pazopanib does not bring remarkable improvement in patients with angiosarcoma (2017) (22)
- An acquired bullous dermatosis due to an autoimmune reaction against uncein (1996) (22)
- Paraneoplastic pemphigus: the first case report from Japan. (1995) (22)
- Anti‐p200 pemphigoid in a 17‐year‐old girl successfully treated with systemic corticosteroid and dapsone (2007) (22)
- Localized linear IgA/IgG bullous dermatosis. (2010) (22)
- Rapid remission of severe pruritus from angiolymphoid hyperplasia with eosinophilia by pulsed dye laser therapy (2003) (22)
- Allogeneic hematopoietic stem cell transplantation following reduced‐intensity conditioning for mycosis fungoides and Sezary syndrome (2016) (22)
- DNA-based prenatal exclusion of harlequin ichthyosis. (2008) (22)
- Severe generalized deep dermatophytosis due to Trichophyton rubrum (trichophytic granuloma) in a patient with atopic dermatitis. (2004) (22)
- A novel GJB2 mutation p.Asn54His in a patient with palmoplantar keratoderma, sensorineural hearing loss and knuckle pads. (2007) (22)
- Dermoscopic features of plasma cell cheilitis and actinic cheilitis. (2014) (22)
- Gap junction development in the human fetal hair follicle and bulge region (2004) (22)
- Comparative study of bullous pemphigoid antigens among Japanese, British, and U.S. patients indicates similar antigen profiles with the 170-kD antigen present both in the basement membrane and on the keratinocyte cell membrane. (1993) (21)
- Cutaneous pemphigus vulgaris with skin features similar to the classic mucocutaneous type: a case report and review of the literature (2008) (21)
- Pigment epithelium-derived factor prevents melanoma growth via angiogenesis inhibition. (2008) (21)
- Eccrine porocarcinoma and Bowen's disease arising in a seborrhoeic keratosis (2006) (21)
- C-Terminal Processing of Collagen XVII Induces Neoepitopes for Linear IgA Dermatosis Autoantibodies. (2017) (21)
- Possible involvement of exon 31 alternative splicing in phenotype and severity of epidermolysis bullosa caused by mutations in PLEC1. (2007) (21)
- Wells' syndrome as a manifestation of hypereosinophilic syndrome (2002) (21)
- Amicrobial pustulosis associated with IgA nephropathy and Sjögren's syndrome. (2007) (21)
- Immunohistochemical study of mixed tumor of the skin with marked ossification. (1996) (21)
- Novel compound heterozygous nonsense and missense ABCA12 mutations lead to nonbullous congenital ichthyosiform erythroderma (2008) (21)
- Dystrophic form of inherited epidermolysis bullosa in a dog (Akita Inu) (1995) (21)
- Colocalization of Multiple Laminin Isoforms Predominantly beneath Hemidesmosomes in the Upper Lamina Densa of the Epidermal Basement Membrane (2006) (21)
- Increase in macrophage migration inhibitory factor levels in lacrimal fluid of patients with severe atopic dermatitis (2006) (20)
- A novel homozygous mutation 371delA in TGM1 leads to a classic lamellar ichthyosis phenotype (2003) (20)
- Rituximab therapy for refractory autoimmune bullous diseases: A multicenter, open‐label, single‐arm, phase 1/2 study on 10 Japanese patients (2019) (20)
- Macropinocytosis of type XVII collagen induced by bullous pemphigoid IgG is regulated via protein kinase C (2016) (20)
- Partially disturbed lamellar granule secretion in mild congenital ichthyosiform erythroderma with ALOX12B mutations (2010) (20)
- PCTAIRE1/CDK16/PCTK1 is overexpressed in cutaneous squamous cell carcinoma and regulates p27 stability and cell cycle. (2017) (20)
- Difference in binding sites of autoantibodies against 230- and 170-kD bullous pemphigoid antigens on salt-split skin. (1994) (20)
- Analysis of the COL17A1 in non-Herlitz junctional epidermolysis bullosa and amelogenesis imperfecta. (2006) (20)
- Mycosis fungoides with marked hyperpigmentation. (1996) (20)
- Type VII collagen deficiency causes defective tooth enamel formation due to poor differentiation of ameloblasts. (2012) (20)
- Intravenous pyogenic granuloma of the hand. (2001) (20)
- Tropical-Wood-Induced Bullous Erythema multiforme (2000) (20)
- Evidence for pathogenicity of autoreactive T cells in autoimmune bullous diseases shown by animal disease models (2012) (19)
- A novel ABCA12 mutation 3270delT causes harlequin ichthyosis (2006) (19)
- Direct Immunofluorescence Using Non-Lesional Buccal Mucosa in Mucous Membrane Pemphigoid (2018) (19)
- Expression of plectin and HD1 epitopes in patients with epidermolysis bullosa simplex associated with muscular dystrophy (1999) (19)
- A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease (2019) (19)
- Circumscribed palmar hypokeratosis: correlation between histopathological patterns and dermoscopic findings (2012) (19)
- Direct injection of naked DNA and cytokine transgene expression: implications for keratinocyte gene therapy (2002) (19)
- Eccrine porocarcinoma and eccrine poroma arising in a scar (2004) (19)
- MUC5AC expression correlates with invasiveness and progression of extramammary Paget's disease (2014) (19)
- Cutaneous manifestations of Helicobacter cinaedi infection. (2013) (19)
- A novel keratin K5 gene mutation in Dowling-Meara epidermolysis bullosa simplex. (1996) (19)
- Cultured epidermal autografts from clinically revertant skin as a potential wound treatment for recessive dystrophic epidermolysis bullosa. (2019) (19)
- Severe refractory chronic actinic dermatitis successfully treated with tacrolimus ointment (2002) (19)
- Aggressive squamous cell carcinoma developing in a giant epidermal cyst of the abdomen (2006) (19)
- Combined features of pemphigus foliaceus and bullous pemphigoid: immunoblot and immunoelectron microscopic studies. (1995) (19)
- Successful treatment of hidradenitis suppurativa with rituximab for a patient with idiopathic carpotarsal osteolysis and chronic active antibody‐mediated rejection (2018) (18)
- Epidermolysis bullosa in Japan. (2010) (18)
- Congenital ichthyosiform erythroderma mimicking ichthyosis bullosa of Siemens (2007) (18)
- An infantile case of pityriasis lichenoides et varioliformis acuta (2007) (18)
- BP180 Autoantibodies Target Different Epitopes in Multiple Sclerosis or Alzheimer's Disease than in Bullous Pemphigoid. (2019) (18)
- Compound Heterozygous ABCA12 Mutations Including a Novel Nonsense Mutation Underlie Harlequin Ichthyosis (2007) (18)
- Collodion baby: ultrastructure and distribution of cornified cell envelope proteins and keratins. (1997) (18)
- Immunoelectron microscopy of skin basement membrane zone antigens: a pre-embedding method using 1-nm immunogold with silver enhancement. (1994) (18)
- [White fibrous papulosis of the neck; review of our 16 cases]. (1985) (18)
- DNA-based prenatal exclusion of bullous congenital ichthyosiform erythroderma at the early stage, 10 to 11 weeks' of pregnancy, in two consequent siblings. (2004) (18)
- Macrophage migration inhibitory factor in zinc-allergic systemic contact dermatitis. (2006) (18)
- Eosinophilic annular erythema is clinically characterized by central pigmentation reflecting basal melanosis: a clinicopathological study of 10 cases (2017) (18)
- Polymorphism in the tumor necrosis factor B gene is associated with Palmoplantar pustulosis. (1999) (17)
- Erythrokeratoderma variabilis without connexin 31 or connexin 30.3 gene mutation: immunohistological, ultrastructural and genetic studies. (2003) (17)
- Possible role of endoplasmic reticulum stress in the pathogenesis of Darier's disease. (2006) (17)
- Two cases of atypical melanocytic lesions in recessive dystrophic epidermolysis bullosa infants (2005) (17)
- Nail deformity associated with hereditary multiple exostoses. (2005) (17)
- Absence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosa (1997) (17)
- Papuloerythroderma of Ofuji associated with early gastric cancer (2008) (17)
- New insight into genotype/phenotype correlations in ABCA12 mutations in harlequin ichthyosis. (2011) (17)
- Lichen striatus affecting a mother and her son. (2005) (17)
- Clinical and immunological features of pemphigus relapse (2019) (17)
- Epidermolysis bullosa acquisita: report of a case with comparison of immunogold electron microscopy using pre‐ and postembedding labelling (1996) (17)
- Novel mutation p.Gly59Arg in GJB6 encoding connexin 30 underlies palmoplantar keratoderma with pseudoainhum, knuckle pads and hearing loss (2009) (17)
- Epidermolysis bullosa: directions for future research and new challenges for treatment (2003) (17)
- 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 (2002) (16)
- Loss of interaction between plectin and type XVII collagen results in epidermolysis bullosa simplex (2017) (16)
- Epidermal aspects of type VII collagen: Implications for dystrophic epidermolysis bullosa and epidermolysis bullosa acquisita (2018) (16)
- Metastasis of lung cancer to the finger: a report of two cases (2005) (16)
- Dipeptidyl Peptidase-4 Inhibitor-associated Bullous Pemphigoid: Recurrence with Epitope Spreading. (2018) (16)
- Transglutaminase1 preferred substrate peptide K5 is an efficient tool in diagnosis of lamellar ichthyosis. (2010) (16)
- Immunofluorescence studies using skin sections of recessive dystrophic epidermolysis bullosa patients indicated that the antigen of anti-p200 pemphigoid is not a fragment of type VII collagen. (2003) (16)
- Preferential Reactivity of Dipeptidyl Peptidase-IV Inhibitor-Associated Bullous Pemphigoid Autoantibodies to the Processed Extracellular Domains of BP180 (2019) (16)
- Intravenous IgG Reduces Pathogenic Autoantibodies, Serum IL-6 Levels, and Disease Severity in Experimental Bullous Pemphigoid Models. (2018) (16)
- Prenatal diagnosis of tyrosinase-negative oculocutaneous albinism (1992) (16)
- Sequential Local Injection of Low-Dose Interferon-Beta for Maintenance Therapy in Stage II and III Melanoma: A Single-Institution Matched Case-Control Study (2012) (16)
- Generalized exacerbation of systemic allergic dermatitis due to zinc patch test and dental treatments (2010) (16)
- Intravascular Histiocytosis Associated with Rheumatoid Arthritis (2008) (16)
- Chain saw blade granuloma: reaction to a deeply embedded metal fragment. (2006) (16)
- Plaquelike cutaneous lupus mucinosis. (1993) (16)
- Two cases of folliculosebaceous cystic hamartoma (2006) (16)
- Multicentric reticulohistiocytosis associated with rheumatoid arthritis (2005) (15)
- Polymorphisms in the muscarinic receptor 1 gene confer susceptibility to asthma in Japanese subjects. (2006) (15)
- Context-Dependent Regulation of Collagen XVII Ectodomain Shedding in Skin. (2015) (15)
- Consequences of two different amino-acid substitutions at the same codon in KRT14 indicate definitive roles of structural distortion in epidermolysis bullosa simplex pathogenesis. (2011) (15)
- Birt–Hogg–Dubé syndrome with clear‐cell and oncocytic renal tumour and trichoblastoma associated with a novel FLCN mutation (2009) (15)
- Recurrence of hydroxyurea-induced leg ulcer after discontinuation of treatment. (2011) (15)
- A case of lichen amyloidosis treated with pulsed dye laser (2005) (15)
- Human monoclonal anti‐basement membrane zone antibodies derived from virally transformed lymphocytes of a patient with bullous pemphigoid recognize epitopes associated with hemidesmosomes (1991) (15)
- Topical application of dehydroxymethylepoxyquinomicin improves allergic inflammation via NF-kappaB inhibition. (2010) (15)
- Epidermodysplasia verruciformis and generalized verrucosis: the same disease? (2006) (15)
- 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 (2019) (15)
- Prurigo pigmentosa. Case report with an electron microscopic observation. (1985) (15)
- Immunohistochemical evaluation of epidermis overlying basal cell carcinomas (1993) (15)
- A Severe and Refractory Case of Anti-p200 Pemphigoid Resulting in Multiple Skin Ulcers and Scar Formation (2008) (15)
- A case of linear IgA bullous dermatosis of childhood: immunoelectron microscopic and IgA subclass studies. (1990) (15)
- A novel leucine to valine mutation in residue 7 of the helix initiation motif of keratin10 leads to bullous congenital ichthyosiform erythroderma. (2001) (15)
- Oral mucosa is a useful substrate for detecting autoantibodies of mucous membrane pemphigoid (2018) (15)
- Prevalent founder mutation c.736T>A of LIPH in autosomal recessive woolly hair of Japanese leads to variable severity of hypotrichosis in adulthood (2013) (15)
- Three‐base deletion mutation c.120_122delGTT in ATP2A2 leads to the unique phenotype of comedonal Darier disease (2010) (15)
- Controlling the histological margin for non‐melanoma skin cancer conveniently using a double‐bladed scalpel (2010) (15)
- Cutaneous manifestations of Helicobacter cinaedi: a review (2016) (14)
- Bowen's disease of the nail matrix presenting as melanonychia: detection of human papillomavirus type 56. (2009) (14)
- Increased macrophage migration inhibitory factor (MIF) in the sera of patients with extensive alopecia areata. (2002) (14)
- Glycosylation Specific for Adhesion Molecules in Epidermis and Its Receptor Revealed by Glycoform-focused Reverse Genomics *S (2009) (14)
- Wells' syndrome associated with chronic myeloid leukaemia. (2013) (14)
- Altered lipid profiles in the stratum corneum of Sjögren-Larsson syndrome. (2011) (14)
- Melanoma antigen A12 regulates cell cycle via tumor suppressor p21 expression. (2017) (14)
- Histology of fetal eyes with oculocutaneous albinism. (1996) (14)
- Keratosis follicularis squamosa (Dohi): a follicular keratotic disorder well known in Japan (2001) (14)
- Establishment of integration-free induced pluripotent stem cells from human recessive dystrophic epidermolysis bullosa keratinocytes. (2017) (14)
- Prenatal diagnosis of epidermolysis bullosa: first successful trial in Asia. (1994) (14)
- Dermoscopy of pseudoxanthoma elasticum-like papillary dermal elastolysis. (2013) (14)
- Abnormal cornified cell envelope formation in mutilating palmoplantar keratoderma unrelated to epidermal differentiation complex. (1998) (14)
- Anti-idiotypic Antibodies against BP-IgG Prevent Type XVII Collagen Depletion (2017) (14)
- Eosinophilic folliculitis in a patient after allogeneic bone marrow transplantation: Case report and review of the literature (2004) (13)
- Pathogenesis of bullous pemphigoid. (2011) (13)
- Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study (2021) (13)
- Scrotal metastases originating from colorectal carcinoma (2003) (13)
- Ultrastructural features of trafficking defects are pronounced in melanocytic nevus in Hermansky-Pudlak syndrome type 1. (2005) (13)
- Immunomapping of EBA sera to multiple epitopes on collagen VII: further evidence that anchoring fibrils originate and terminate in the lamina densa (2003) (13)
- Linear verrucous haemangioma on the abdomen. (2003) (13)
- Cutaneous Manifestations of Thymoma-associated Multi-organ Autoimmunity: A Fatal Sign. (2016) (13)
- Bone marrow-derived cells are not the origin of the cancer stem cells in ultraviolet-induced skin cancer. (2009) (13)
- An elderly patient with mycosis fungoides successfully treated with chronic low‐dose oral etoposide therapy (2004) (13)
- Mucous membrane pemphigoid with generalized blisters: IgA and IgG autoantibodies target both laminin‐332 and type XVII collagen (2012) (13)
- Simultaneous occurrence of three squamous cell carcinomas in a recessive dystrophic epidermolysis bullosa patient. (2003) (13)
- Evaluation of the clinical usefulness of measuring urinary excretion of 5-S-cysteinyldopa in melanoma: ten years' experience of 50 patients. (1997) (13)
- Pagetoid dyskeratosis with parallel ridge pattern under dermoscopy. (2013) (13)
- Autoantibodies of non‐inflammatory bullous pemphigoid hardly deplete type XVII collagen of keratinocytes (2017) (13)
- Two cases of erosive oral lichen planus with autoantibodies to desmoglein 3 (2016) (13)
- Intravenous injection of Muse cells as a potential therapeutic approach for epidermolysis bullosa. (2020) (13)
- A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2). (2003) (13)
- Punctate palmoplantar keratoderma type 1: a novel AAGAB mutation and efficacy of etretinate. (2015) (13)
- The direct binding of collagen XVII and collagen IV is disrupted by pemphigoid autoantibodies (2018) (13)
- Giant dermatofibroma: a rare variant of dermatofibroma preferentially developing on the lower limbs (2006) (13)
- Squamous cell carcinoma in a patient with non‐bullous congenital ichthyosiform erythroderma (2003) (13)
- Pyoderma Gangrenosum of the Eyelid: Report of Two Cases and Review of the Literature (2010) (12)
- Prenatal diagnosis of tyrosinase‐negative oculocutaneous albinism by an electron microscopic dopa reaction test of fetal skin (1994) (12)
- Novel ALDH3A2 heterozygous mutations in a Japanese family with Sjögren-Larsson syndrome. (2006) (12)
- Perforating Granuloma Annulare (1985) (12)
- Compound heterozygotes for filaggrin gene mutations do not always show severe atopic dermatitis (2017) (12)
- The β9 loop domain of PA-PLA1α has a crucial role in autosomal recessive woolly hair/hypotrichosis. (2012) (12)
- Ultrasonographic findings can identify ‘pseudoprogression’ under nivolumab therapy (2017) (12)
- Rapid remission of severe pain from livedoid vasculopathy by apixaban (2017) (12)
- Cutaneous chronic graft-versus-host disease localized to the field of total lymphoid irradiation. (1996) (12)
- Kindler's syndrome with recurrence of bullae in the fifth decade (1996) (12)
- Somatic recombination underlies frequent revertant mosaicism in loricrin keratoderma (2019) (12)
- Galectin-7 as a potential biomarker of Stevens-Johnson syndrome/toxic epidermal necrolysis: identification by targeted proteomics using causative drug-exposed peripheral blood cells. (2019) (12)
- Severe cholinergic urticaria successfully treated with scopolamine butylbromide in addition to antihistamines (2006) (12)
- Electron microscopic DOPA reaction test for oculocutaneous albinism (2000) (12)
- Anti-laminin-gamma 1 Pemphigoid with Generalized Pustular Psoriasis and Psoriasis Vulgaris. (2016) (12)
- Combination of a novel frameshift mutation (1929delCA) and a recurrent nonsense mutation (W610X) of the LAMB3 gene in a Japanese patient with Herlitz junctional epidermolysis bullosa, and their application for prenatal testing. (1998) (12)
- Multiple fixed drug eruption caused by acetaminophen (2003) (12)
- Durable Remission of Sézary Syndrome after Unrelated Bone Marrow Transplantation by Reduced-Intensity Conditioning (2008) (12)
- Novel mutation in a fumalate hydratase gene of a Japanese patient with multiple cutaneous and uterine leiomyomatosis. (2007) (12)
- Immunomolecular mapping of adherens junction and desmosomal components in normal human epidermis (2003) (12)
- Generalized acute subcutaneous edema as a rare cutaneous manifestation of severe dermatomyositis (2016) (12)
- Disturbed balance in three subpopulations of CD4(+)Foxp3(+) regulatory T cells in Stevens-Johnson syndrome and toxic epidermal necrolysis patients. (2013) (12)
- DNA vaccination against macrophage migration inhibitory factor improves atopic dermatitis in murine models. (2009) (11)
- Plasma exchange; a promising treatment for toxic epidermal necrolysis with AIDS. (2004) (11)
- Pyloric atresia‐junctional epidermolysis bullosa syndrome showing novel 594insC/Q425P mutations in integrin β4 gene (ITGB4) (2004) (11)
- Dermoscopic findings of irritated seborrheic keratosis (2016) (11)
- Compound heterozygous missense mutations p.Leu207Pro and p.Tyr544Cys in TGM1 cause a severe form of lamellar ichthyosis (2018) (11)
- Treatment for poikilodermatous erythema of dermatomyositis with the pulsed dye laser (2005) (11)
- Complete paternal isodisomy of chromosome 17 in junctional epidermolysis bullosa with pyloric atresia. (2010) (11)
- A founder effect of c.1938delC in ITGB4 underlies junctional epidermolysis bullosa and its application for prenatal testing (2011) (11)
- Tumour‐like muscular sarcoidosis (2007) (11)
- Spitz naevus of the glans penis: an unusual location. (2004) (11)
- Dermoscopic features of hidroacanthoma simplex: Usefulness in distinguishing it from Bowen's disease and seborrheic keratosis (2015) (11)
- Histochemical analysis of macrophage migration inhibitory factor in psoriasis vulgaris (2002) (11)
- Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome. (2011) (11)
- Long-term follow-up of cultured epidermal autograft in a patient with recessive dystrophic epidermolysis bullosa. (2014) (11)
- Conradi–Hünermann–Happle syndrome with abnormal lamellar granule contents (2009) (11)
- High Expression of Collagen XVII Compensates for its Depletion Induced by Pemphigoid IgG in the Oral Mucosa. (2018) (11)
- Characteristics of IgG subclasses and complement deposition in BP230‐type bullous pemphigoid (2018) (11)
- Extremely severe palmoplantar hyperkeratosis in a generalized epidermolytic hyperkeratosis patient with a keratin 1 gene mutation. (2011) (11)
- Novel adenosine triphosphate (ATP)‐binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma (2012) (11)
- Multiple Nodular Lesions Seen in a Patient with Neurocutaneous Melanosis (1996) (11)
- Application of an image analyzer to gold labeling in immunoelectron microscopy to achieve better demonstration and quantitative analysis. (1993) (11)
- A novel asparagine-->aspartic acid mutation in the rod 1A domain in keratin 2e in a Japanese family with ichthyosis bullosa of Siemens. (2000) (11)
- Evaluation of immunoelectron microscopic techniques in the study of basement membrane antigens (1998) (10)
- A Japanese case of the fibrillar type of dermatitis herpetiformis. (1995) (10)
- Morphological and genetic analysis of steatocystoma multiplex in an Asian family with pachyonychia congenita type 2 harbouring a KRT17 missense mutation (2009) (10)
- Mucocutaneous pyoderma gangrenosum due to trisomy 8 neutrophilic infiltrates in a patient with myelodysplastic syndrome (2016) (10)
- Keratotic lesions in epidermolysis bullosa simplex with mottled pigmentation. (2005) (10)
- Erythema annulare centrifugum-like neutrophilic dermatosis: effects of potassium iodide. (2012) (10)
- Structural, enzymatic and molecular studies in a series of nonbullous congenital ichthyosiform erythroderma patients (2005) (10)
- Papuloerythroderma associated with hepatitis C virus infection. (2005) (10)
- Ultrasound B‐mode and elastographic findings of angiomatoid fibrous histiocytoma (2014) (10)
- Skipped exon in COL7A1 determines the clinical phenotypes of dystrophic epidermolysis bullosa (2015) (10)
- Ramucirumab-induced Multiple Haemangiomas of the Skin: Two Case Reports. (2018) (10)
- Neonatal vesiculopustular eruption of the face: a sign of trisomy 21‐associated transient myeloproliferative disorder (2007) (10)
- Novel premature termination codon mutations in the laminin gamma2-chain gene (LAMC2) in Herlitz junctional epidermolysis bullosa. (1998) (10)
- Detection of mucous membrane pemphigoid autoantibodies by full-length BP180 enzyme-linked immunosorbent assay. (2017) (10)
- Contact dermatitis due to eugenol used to treat oral lichen planus (2003) (10)
- Intraepidermal neutrophilic IgA pemphigus successfully treated with dapsone. (2012) (10)
- Unilateral periorbital oedema due to sarcoid infiltration of the eyelid: an unusual presentation of sarcoidosis with facial nerve palsy and parotid gland enlargement (2007) (10)
- Electron microscopy in diagnosis of autoimmune bullous disorders. (2001) (10)
- Prenatal diagnosis of inherited skin diseases. (1996) (10)
- Annular Lichen planus: Study of the Cellular Mechanisms of Annularity (2004) (10)
- Warty intralymphatic histiocytosis successfully treated with topical tacrolimus (2015) (10)
- Immunohistochemical and Ultrastructural Studies (1993) (10)
- Combination of novel premature termination codon and glycine substitution mutations in COL7A1 leads to moderately severe recessive dystrophic epidermolysis bullosa. (2000) (10)
- Histone deacetylase inhibitors preferentially augment transient transgene expression in human dermal fibroblasts (2007) (10)
- ITGB4 missense mutation in a transmembrane domain causes non-lethal variant of junctional epidermolysis bullosa with pyloric atresia. (2007) (10)
- A novel indel COL7A1 mutation 8068del17insGA causes dominant dystrophic epidermolysis bullosa (2006) (10)
- Dermoscopic observation in adenoma of the nipple (2015) (10)
- Dermoscopy of periungual pigmented Bowen's disease: its usefulness in differentiation from malignant melanoma (2016) (9)
- Localized bullous pemphigoid associated with dipeptidyl peptidase-4 inhibitor treatment (2018) (9)
- Potential role of extracellular vesicle-mediated antigen presentation in Helicobacter pylori hypersensitivity during eradication therapy. (2018) (9)
- Transglutaminase and major cornified cell envelope precursor proteins, loricrin, small proline-rich proteins 1 and 2, and involucrin are coordinately expressed in the sites defined to form hair canal in developing human hair follicle. (1999) (9)
- Characteristic findings of handprint and dermoscopy in reticulate acropigmentation of Kitamura (2014) (9)
- Spontaneous Remission of Solitary-Type Infantile Myofibromatosis (2011) (9)
- Bullous pemphigoid developed in a patient with prurigo nodularis (2017) (9)
- Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagen (2011) (9)
- Compound heterozygosity for novel splice site mutations of ITGA6 in lethal junctional epidermolysis bullosa with pyloric atresia (2017) (9)
- Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa (2006) (9)
- Current advances in gene therapy for the treatment of genodermatoses. (2009) (9)
- Cultured keratinocytes from plectin/HD1-deficient epidermolysis bullosa simplex showed altered ability of adhesion to the matrix. (2000) (9)
- Multiple apocrine hidrocystoma showing plane pigmented macules. (2006) (9)
- Compound heterozygosity for a point mutation and a deletion located at splice acceptor sites in the LAMB3 gene leads to generalized atrophic benign epidermolysis bullosa. (2000) (9)
- Generalized pustular psoriasis and Hepatitis C virus infection. (2004) (9)
- Coexistence of pustular and vegetative pyoderma gangrenosum in a patient with myelodysplastic syndrome. (2012) (9)
- Epidermal vacuolation: An artifact due to injection of local anesthetics (2004) (9)
- Glycine substitution mutations by different amino acids at the same codon in COL7A1 cause different modes of dystrophic epidermolysis bullosa inheritance (2006) (9)
- Hereditary benign telangiectasia: two families with punctate telangiectasias surrounded by anemic halos. (2010) (9)
- AKT has an anti-apoptotic role in ABCA12-deficient keratinocytes. (2011) (8)
- Expression of transglutaminase 1 (transglutaminase K) in harlequin ichthyosis (1997) (8)
- Filaggrin gene mutations may influence the persistence of food allergies in Japanese primary school children (2018) (8)
- Pigmented skin metastasis of breast cancer showing dermoscopic features of malignant melanoma (2015) (8)
- Efficacy of N‐(3,4‐dimethoxycinnamoyl)‐anthranilic acid (tranilast) against eruptive syringoma: Report of two cases and review of published work (2012) (8)
- COL7A1 mutation G2037E causes epidermal retention of type VII collagen (2006) (8)
- Chromosomal inversions as a hidden disease-modifying factor for somatic recombination phenotypes. (2018) (8)
- DNA‐based prenatal diagnosis of plectin‐deficient epidermolysis bullosa simplex associated with pyloric atresia (2011) (8)
- Thymoma‐associated multi‐organ autoimmunity: two cases and a review of the literature (2017) (8)
- Altered balance of epidermis-related chemokines in epidermolysis bullosa. (2017) (8)
- Type XVII collagen interacts with the aPKC‐PAR complex and maintains epidermal cell polarity (2020) (8)
- R278TER and P431L mutations of the tyrosinase gene exist in Japanese patients with tyrosinase-negative oculocutaneous albinism. (1996) (7)
- Loss‐of‐function mutations in the gene encoding filaggrin underlie a Japanese family with food‐dependent exercise‐induced anaphylaxis (2015) (7)
- A possible association between BP230‐type bullous pemphigoid and dementia: a report of two cases in elderly patients (2018) (7)
- Cutaneous reactions to imatinib mesylate treated by topical steroid (2005) (7)
- Heterogeneous reactivity with LH7.2 and the first prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa among Japanese patients. (1996) (7)
- Portable negative‐pressure wound therapy for pyoderma gangrenosum: Report of two cases (2018) (7)
- Dipeptidyl peptidase‐4 inhibitor‐associated bullous pemphigoid in a patient with acquired reactive perforating collagenosis (2018) (7)
- Recent advances in electron microscopic immunocytochemistry in dermatology (1993) (7)
- Striate palmoplantar keratoderma: Report of a novel DSG1 mutation and atypical clinical manifestations. (2015) (7)
- Two cases of cutaneous sporotrichosis in continental/microthermal climate zone: global warming alert? (2010) (7)
- Acquired perforating dermatosis appearing as elastosis perforans serpiginosa and perforating folliculitis (2008) (7)
- The identification of autoantigens in mucous membrane pemphigoid using immortalized oral mucosal keratinocytes (2018) (7)
- The different intensity of autoantibody deposits in bullous pemphigoid associated with psoriasis vulgaris (2015) (7)
- Conversion from human haematopoietic stem cells to keratinocytes requires keratinocyte secretory factors (2012) (7)
- Indomethacin for refractory infantile eosinophilic pustular folliculitis. (2013) (7)
- Vesicular pemphigoid--ultrastructural and immunoelectron microscopic study. (1989) (7)
- Detection of circulating lymphoma cells in subcutaneous panniculitis‐like T‐cell lymphoma (2003) (7)
- Cryofixed, freeze-dried and paraffin-embedded skin enables successful immunohistochemical staining of skin basement membrane antigens (1992) (7)
- Three Cases of Darier’s Disease in a Family Showing Marked Heterogeneous Clinical Severity (1999) (7)
- Filaggrin: an emerging star in atopic march. (2008) (7)
- Ultrasonographic features of intravascular fasciitis: case report and review of the literature (2017) (7)
- Genetic analysis of a novel splice‐site mutation in TMC8 reveals the in vivo importance of the transmembrane channel‐like domain of TMC8 (2016) (7)
- Regulatory T cell subsets in bullous pemphigoid and dipeptidyl peptidase-4 inhibitor-associated bullous pemphigoid. (2020) (7)
- Dermoscopy is useful for bed bug (Cimex lectularius) bites (2016) (7)
- Granulomatous blepharitis successfully treated with tranilast (2003) (7)
- The Unique Dermoscopic Structure ‘Large black web’ in basal cell carcinoma on the areola (2016) (7)
- Disruption of the suprabasal keratin network by mutation M150T in the helix initiation motif of keratin 10 does not affect cornified cell envelope formation in human epidermis (2003) (7)
- Higher density of label-retaining cells in gingival epithelium. (2009) (7)
- 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. (2013) (7)
- mTOR expression correlates with invasiveness and progression of extramammary Paget's disease (2014) (7)
- X-linked recessive inheritance in a family with isolated congenital alopecia (1996) (6)
- Plasma cell cheilitis extending beyond vermillion border (2015) (6)
- Pazopanib can preserve cosmetic quality of life even in end‐stage angiosarcoma (2015) (6)
- Trichilemmal carcinoma in situ. (1998) (6)
- Bilateral axillary Paget’s disease: diagnostic pitfalls of dermoscopic features (2014) (6)
- Bullous pemphigoid associated with psoriasis showing marked neutrophilic infiltrates (2020) (6)
- Diagnostic features of acquired dermal melanocytosis of the face and extremities (2018) (6)
- Modified Dufourmentel flap, easy to design and tailor to the defect (2017) (6)
- Hair colour shampoo dermatitis (2017) (6)
- Epidermal melanocytes in normal and tyrosinase-negative oculocutaneous albinism fetuses (2004) (6)
- The use of ELISA to detect desmoglein antibodies in a pregnant woman and fetus. (2003) (6)
- Bloody nipple discharge in an infant. (2009) (6)
- Immune Reaction to Type XVII Collagen Induces Intramolecular and Intermolecular Epitope Spreading in Experimental Bullous Pemphigoid Models (2019) (6)
- Prolonged dermatitis distant to the site of squaric acid dibutyl ester applications and recovery of alopecia areata (2005) (6)
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa. (2005) (6)
- Low‐dose etretinate shows promise in management of punctate palmoplantar keratoderma type 1: Case report and review of the published work (2015) (6)
- Prenatal diagnosis of epidermolysis bullosa (2006) (6)
- Intractable erythema nodosum associated with severe breast abscesses: reports of two cases (2005) (6)
- Autoantibodies undetectable by chemiluminescent enzyme immunoassay require extended antigen–antibody reaction time for detection (2018) (6)
- Dermoscopic features of tungiasis (2018) (6)
- Melanoma antigen A12 regulates cell cycle via tumor suppressor p21 expression (2017) (6)
- Identification of SERPINB7 mutations in Korean patients with Nagashima‐type palmoplantar keratosis (2017) (6)
- Marked swollen erythema of the face together with sicca syndrome as a sign for chronic active Epstein–Barr virus infection (2000) (6)
- A case of anti-BP230 antibody-positive bullous pemphigoid receiving DPP-4 inhibitor (2020) (6)
- A severe case of mango dermatitis (2018) (6)
- Hair shaft abnormalities in localized autosomal recessive hypotrichosis 2 and a review of other non-syndromic human alopecias. (2011) (6)
- Widespread erythema ab igne caused by hot bathing (2015) (6)
- Tubular apocrine adenoma clinically and dermoscopically mimicking basal cell carcinoma. (2014) (6)
- Linear IgA Bullous Dermatosis in a Pregnant Woman with Autoantibodies to the Non-collagenous 16A Domain of Type XVII Collagen. (2017) (6)
- Acrokeratoelastoidosis successfully treated with 10% salicylic acid ointment (2017) (6)
- Large subcutaneous abscesses caused by Mycobacterium fortuitum infection. (2008) (6)
- Marked and restricted cutaneous pigmentation induced by selective intra-arterial cisplatin infusion. (2006) (6)
- Do pigmented naevi in albinism provide evidence of tyrosinase positivity? (1992) (5)
- CYP4F22 is highly expressed at the site and timing of onset of keratinization during skin development. (2012) (5)
- Expression of macrophage migration inhibitory factor in rat skin during embryonic development (2005) (5)
- A novel OSMR mutation in familial primary localized cutaneous amyloidosis in a Japanese family. (2009) (5)
- Identification of previously unknown SERPINB7 splice variants in patients with Nagashima‐type palmoplantar keratosis reveals the importance of the CD‐loop of SERPINB7 (2015) (5)
- Retrospective study on the correlation between 18‐fluorodeoxyglucose uptake in positron emission tomography–computer tomography and tumour volume, cytological activity as assessed with Ki‐67 and GLUT‐1 staining in 10 cases of Merkel cell carcinoma (2018) (5)
- Macrophage migration inhibitory factor (MIF) in bullous pemphigoid. (2008) (5)
- A subcutaneous tumor on the forehead of a 12-year-old child: a rare clinical presentation of a frontal mucocele. (2004) (5)
- Low‐grade myxofibrosarcoma invaded into the underlying skeletal muscle (2007) (5)
- CD4/CD8 double-negative T-cell lymphoma: a variant of primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma? (2015) (5)
- Medical genetics: An Indian family with Sjögren‐Larsson syndrome caused by a novel ALDH3A2 mutation (2010) (5)
- Hair follicle stem cell progeny heal blisters while pausing skin development (2020) (5)
- Lipofuscin deposition causes the pigmentation of apocrine hidrocystoma (2018) (5)
- Subepidermal blistering disease with 3 distinct autoantibodies: anti-BP230, anti-laminin gamma-1, and anti-laminin-332. (2011) (5)
- Peginterferon alfa-2b for mycosis fungoides. (2006) (5)
- Keratitis-ichthyosis-deafness syndrome lacking subjective hearing impairment. (2008) (5)
- Ultrasound B‐mode and elastographic findings of mixed tumour of the skin on the scalp (2016) (5)
- Solitary fibrous tumour fluctuating in size with menstrual cycle (2014) (5)
- Diagnostic pitfalls of using dermoscopic features to differentiate between malignant melanoma and pigmented seborrhoeic keratosis. (2010) (5)
- Plasma cell cheilitis successfully treated with topical calcineurin inhibitors (2016) (5)
- Autoantibodies against type XVII collagen C‐terminal domain in a patient with bullous pemphigoid associated with psoriasis vulgaris (2009) (5)
- RNA recognition motif of LEMD3 as a key player in the pathogenesis of Buschke-Ollendorff syndrome. (2016) (5)
- Coexistence of a systemic lupus erythematosus and porphyria cutanea tarda: case successfully improved by avoidance of sun exposure (2006) (5)
- Absence of anti-human herpesvirus 8 antibody in 32 Japanese hemophiliacs with advanced HIV infection (2001) (5)
- “Sprinkle brightness lesion” appearance in ultrasound B‐mode findings of sinusoidal hemangioma (2014) (5)
- Two cases of interleukin-7 (IL-7)-deficient generalized verrucosis. (2020) (5)
- Diagnosis of Werner syndrome by immunoblot analysis (2002) (5)
- Precursor B-cell lymphoblastic lymphoma presented with intraocular involvement and unusual skin manifestations (2008) (5)
- Disseminated cutaneous Mycobacterium kansasii infection in an patient infected with the human immunodeficiency virus (2009) (5)
- From epidemiology and genetics to diagnostics, outcome measures, and novel treatments in autoimmune bullous diseases. (2014) (4)
- Aleukemic leukemia cutis with extensive bone involvement. (2010) (4)
- A novel insertion mutation in COL7A1 identified in Hallopeau-Siemens recessive dystrophic epidermolysis bullosa. (2003) (4)
- Localized cutaneous amyloidosis associated with poikilodermatous mycosis fungoides. (2014) (4)
- Non-pulsatile aneurysm of the superficial temporal artery. (1999) (4)
- A novel PTPN11 missense mutation in a patient with LEOPARD syndrome (2009) (4)
- MMP13 can be a useful differentiating marker between squamous cell carcinoma and benign hyperkeratotic lesions in recessive dystrophic epidermolysis bullosa (2015) (4)
- A case of non‐bullous pemphigoid induced by IgG4 autoantibodies targeting BP230 (2020) (4)
- Zonula occludens-1 demonstrates a unique appearance in buccal mucosa over several layers (2021) (4)
- Erythema annulare centrifugum‐like mycosis fungoides after unrelated bone marrow transplantation (2015) (4)
- Two cases of generalized pustular psoriasis complicated by IgG4‐related disease (2018) (4)
- Extensive Eruptive Syringoma After Liver Transplantation. (2018) (4)
- Reticulated acanthoma with sebaceous differentiation (2017) (4)
- Altered replication stress response due to CARD14 mutations promotes recombination-induced revertant mosaicism. (2021) (4)
- Comprehensive cancer-related gene analysis reveals that active KRAS mutation is a prognostic mutation in mycosis fungoides. (2017) (4)
- Diagnosis of Hailey-Hailey disease facilitated by DNA testing: a novel mutation in ATP2C1. (2008) (4)
- Cutis Verticis Gyrata Fluctuation with Atopic Dermatitis Disease Activity. (2017) (4)
- Hallopeau–Siemens dystrophic epidermolysis bullosa due to homozygous 5818delC mutation in the COL7A gene (2013) (4)
- Autoantibody profile differentiates between inflammatory and non-inflammatory bullous pemphigoid (2016) (4)
- Loss of dynamin-related protein 1 (Drp1) does not affect epidermal development or UVB-induced apoptosis but does accelerate UVB-induced carcinogenesis. (2020) (4)
- Drp1 expression levels correlate with clinical stage in extramammary Paget’s disease (2020) (4)
- Case of bullous pemphigoid associated with teneligliptin accompanied by severe mucous membrane involvement (2018) (4)
- Linear IgA/IgG bullous dermatosis with autoantibodies directing the native and processed forms of BP180 (2020) (4)
- Close association of dermatitis herpetiformis and chronic tonsillitis in a Japanese patient without gluten sensitivity. (2001) (4)
- Disseminated subcutaneous nodules alone as manifestations of Churg–Strauss syndrome (2008) (4)
- Safety of ustekinumab for the treatment of psoriasis vulgaris with myotonic dystrophy (2016) (4)
- Linear Congenital Molluscum Contagiosum on the Coccygeal Region (2013) (4)
- Technical advances in prenatal diagnosis of tyrosinase-negative oculocutaneous albinism. (1997) (4)
- Squamous cell carcinoma in a chronic genital ulcer in Behçet's disease. (2010) (4)
- In‐transit metastasis of advanced eccrine porocarcinoma (2015) (4)
- Extensive Erythema and Hyperkeratosis on the Extremities and Lumbar Area as an Unusual Mani-festation of Nagashima-type Palmoplantar Keratosis. (2016) (4)
- A new clinical variant of acquired reactive perforating dermatosis‐like bullous pemphigoid (2018) (4)
- A case of erythroplasia of Queyrat successfully treated with combination carbon dioxide laser vaporization and surgery (2016) (4)
- Compound heterozygosity for premature termination codon and glycine substitution mutations in the COL7A1 gene in Korean siblings with a moderately severe phenotype of recessive dystrophic epidermolysis bullosa. (2003) (4)
- An immunohistochemical and ultrastructural study of an unusual case of multiple non-X histiocytoma. (1988) (4)
- Erythrokeratoderma Variabilis Caused by p.Gly45Glu in Connexin 31: Importance of the First Extracellular Loop Glycine Residue for Gap Junction Function. (2016) (4)
- Perianal cytomegalovirus ulcer following herpes simplex virus in a patient with idiopathic thrombocytopenic purpura treated with immunosuppressants (2005) (4)
- Dermoscopic features of genital pigmented Bowen's disease: Report of a case and review of the published work (2019) (4)
- Xanthoma striatum palmare as an early sign of familial type III hyperlipoproteinemia with an apoprotein E genotype epsilon2/epsilon2. (2003) (4)
- Squamous cell carcinoma of the auricle with rhabdoid features (2009) (4)
- CD30‐positive primary cutaneous anaplastic large‐cell lymphoma and definite squamous cell carcinoma (2009) (4)
- Lichenoid drug eruption caused by clonazepam (2017) (4)
- Kindler syndrome with severe intestinal involvement: a 31-year follow-up. (2014) (4)
- Spatial expression of matrilysin-1 in epidermolysis bullosa-associated and sporadic cutaneous squamous cell carcinomas (2006) (4)
- Classic (non‐AlDS‐related) Kaposi's sarcoma in a Japanese patient, successfully treated with alpha‐2b‐interferon (1995) (4)
- Pruritic Papules Following Lumbar Corset Use: A Quiz. Grover's disease. (2015) (3)
- Multiple skin metastases of amelanotic melanoma originating from the sinonasal mucosa. (2005) (3)
- Seborrheic keratosis arising on an epidermal nevus with HRAS p.G13R mutation (2017) (3)
- Post-embedding immunoelectron microscopy of tissue processed by rapid freezing and freeze-substitution without chemical fixatives. (1991) (3)
- HPV16‐related pigmented Bowen's disease on the palm (2016) (3)
- A Palindromic Motif in the −2084 to −2078 Upstream Region is Essential for ABCA12 Promoter Function in Cultured Human Keratinocytes (2014) (3)
- A new filaggrin gene mutation in a Korean patient with ichthyosis vulgaris (2014) (3)
- Sweet syndrome‐like eruption with prominent dermal leukocytoclasis associated with systemic lupus erythematosus (2015) (3)
- Association of infantile cutaneous haemangioma on the face and neck with respiratory distress in infancy. (2003) (3)
- Scleroedema adultorum associated with sarcoidosis (2009) (3)
- 032 DNA based prenatal diagnosis of recessive dystrophic epidermolysis bullosa: first successful application in a Japanese family (1995) (3)
- Psoriasis vulgaris with fibrokeratoma from pityriasis amiantacea (2017) (3)
- Lichen planus in childhood showing various cutaneous features. (2012) (3)
- Carebastine, an H1‐receptor antagonist, suppresses the expression of macrophage migration inhibitory factor (2008) (3)
- Repeated skin sampling and prolonged incubation period identified cutaneous Mycobacterium chelonae infection on the face in an immunocompetent man (2014) (3)
- Spontaneously resolving granulomatous tattoo reaction in multiple color regions (2014) (3)
- LAMB3 gene transfection into SV40-transformed keratinocytes from patient with Herlitz junctional epidermolysis bullosa (2000) (3)
- Advanced malignant melanoma successfully treated with dacarbazine following anti‐PD‐1/CTLA‐4 treatment (2020) (3)
- A case of linear basal cell carcinoma: evaluation of proliferative activity by immunohistochemical staining of PCTAIRE1 and p27 (2017) (3)
- Successful prenatal exclusion of an unspecified subtype of severe epidermolysis bullosa. (1998) (3)
- Tubular spitz naevus mimicking eccrine spiradenoma. (2014) (3)
- Technique for histological control of surgical margins in lip cancer (2014) (3)
- Chromosome 11q13.5 variant: No association with atopic eczema in the Japanese population. (2010) (3)
- Primary mucinous carcinoma of the skin with in‐transit metastasis (2015) (3)
- Clinical characteristics and outcomes of bullous pemphigoid patients with versus without oral prednisolone treatment (2021) (3)
- Secondary syphilis mimicking warts in an HIV-positive patient (2009) (3)
- Yellow nail syndrome: Nail change reflects disease severity (2012) (3)
- Altered ultrastructural localization of the C-terminus of bullous pemphigoid antigen 2 (BPAG2) in human skin lacking laminin 5 (1998) (3)
- Bullous pemphigoid following the replacement of vildagliptin with anagliptin (2017) (3)
- Rapid response to clinical symptoms in early psoriatic onycho‐pachydermo‐periostitis treated with infliximab (2018) (3)
- Psoriatic onycho‐pachydermo‐periostitis progressing to generalized pustular psoriasis (2012) (3)
- Cutaneous‐type pemphigus vulgaris successfully treated with topical corticosteroids (2016) (3)
- Possible modifier effects of keratin 17 gene mutation on keratitis–ichthyosis–deafness syndrome (2012) (3)
- [Prenatal diagnosis of lethal junctional epidermolysis bullosa by fetal skin biopsy]. (1991) (3)
- Identification of COL7A1 alternative splicing inserting 9 amino acid residues into the fibronectin type III linker domain. (2003) (3)
- Early severe pachyonychia congenita subtype PC‐K6a with a novel mutation in the KRT6A gene (2017) (3)
- Appearance of antidesmocollin 1 autoantibodies leading to a vegetative lesion in a patient with pemphigus vulgaris (2018) (3)
- Psoriasis vulgaris associated with Vogt‐Koyanagi–Harada Syndrome (2001) (3)
- A severe case of X‐linked ichthyosis showing palmar hyperlinearity without FLG mutations (2017) (3)
- Childhood subepidermal blistering disease with autoantibodies to type VII collagen and laminin‐332 (2011) (3)
- Epidermolysis Bullosa (EB) - Diagnosis and Therapy (2009) (3)
- Ulcerative contact dermatitis caused by benzethonium chloride (2017) (3)
- Novel COL7A1 mutation in a family with bullous dermolysis of the newborn: Phenotypic variability associated with a COL7A1 mutation within the same family (2018) (3)
- Linear IgA Bullous Dermatosis Associated with Immunoglobulin Light-chain Amyloidosis. (2017) (3)
- Two cases of melanomas paradoxically metastasizing to the intestinal tract during nivolumab therapy (2017) (3)
- A recurrent 'hot spot' glycine substitution mutation, G2043R in COL7A1, induces dominant dystrophic epidermolysis bullosa associated with intracytoplasmic accumulation of pro-collagen VII. (2014) (3)
- Acute vascular reaction due to lipo‐prostaglandin E1 (2018) (3)
- A novel ATP2A2 missense mutation p.Asp254Gly in Darier disease restricted to the extremities. (2008) (3)
- Mucosal hyperpigmentation from prophylactic minocycline for EGFR inhibitor (2016) (3)
- G2028R mutation in COL7A1 leads to marked heterogeneous clinical phenotypes of dominant dystrophic epidermolysis bullosa (2002) (3)
- Prevalence of infectious diseases in patients with autoimmune blistering diseases (2020) (3)
- Solitary Piloleiomyoma with an Unusual Clinical Appearance (1996) (3)
- Bone marrow transplantation restores deficient epidermal basement membrane protein and improves the clinical phenotype in epidermolysis bullosa model mice (2009) (3)
- Hypertrophic lupus erythematosus successfully treated with hydroxychloroquine (2017) (2)
- Intractable erythematous plaques on the hands: palmoplantar eosinophilic pustular folliculitis (2013) (2)
- Collagen deposition assessment in burn scar tissue using second harmonic generation and multi-photon microscopy (2010) (2)
- Nodular morphoea: a first case associated with linear morphoea (2016) (2)
- Anti-BP180-type mucous membrane pemphigoid: report of two cases (2014) (2)
- Unique mouse monoclonal antibodies reactive with maturation‐related epitopes on type VII collagen (2017) (2)
- A case of mucous membrane pemphigoid with anti‐BP230 autoantibodies alone (2020) (2)
- Refractory oral ulcers in eosinophilic granulomatosis with polyangiitis (2019) (2)
- Pigmented purpuric dermatosis in mixed cryoglobulinaemia associated with rheumatoid arthritis and hepatitis C infection. (2005) (2)
- Remodeling of desmosomal and hemidesmosomal adhesion systems during human hair follicle development. (2004) (2)
- Severely hyperkeratotic erythroderma associated with Hodgkin's disease: does a high serum level of granulocyte-colony stimulating factor contribute to formation of skin lesions? (2003) (2)
- Epitope spreading possibly from BP230 to the NC16A domain of BP180 preceding disease progression in bullous pemphigoid (2020) (2)
- Proliferating trichilemmal cyst of the mamma (2017) (2)
- Unusual cutaneous manifestations of Churg-Strauss syndrome mimicking Wells' syndrome. (2012) (2)
- Coexistence case of bullous pemphigoid and pemphigus foliaceus. (2013) (2)
- A case of bullous pemphigoid with antidesmoplakin autoantibodies. (1994) (2)
- Renal failure in dogs kept by a man with severe psoriasis (2017) (2)
- N-Linked neutral oligosaccharides in the stratum corneum of normal and ichthyotic skin (2006) (2)
- Disappearing subcutaneous papules and nodules: Characteristic features of muscle herniation and piezogenic pedal papules (2017) (2)
- Metal implant‐induced skin ulcer mimicking scrofuloderma (2016) (2)
- Progressive refractory ulcer of the nipple: a quiz. (2009) (2)
- Maculopapular drug eruption induced by linagliptin (2018) (2)
- Altered expression of actin and focal adhesion-associated proteins in Kindler syndrome (2004) (2)
- A case of toxic epidermal necrolysis with extensive intestinal involvement (2014) (2)
- Pemphigus foliaceus associated with oesophageal cancer (2009) (2)
- Type XVII collagen ELISA indices significantly decreased after bullous pemphigoid remission (2011) (2)
- An erythematous plaque on the breast: a quiz. Solitary T-cell pseudolymphoma, superficial type. (2013) (2)
- Psoriasiform mycosis fungoides masquerading as tumourous plaques (2017) (2)
- Mycosis fungoides bullosa. Commentary (2006) (2)
- Lymphangiosarcoma with strong positivity of D2‐40 and LYVE‐1 presenting different clinical features from angiosarcoma (2014) (2)
- Human type VII collagen harbors multiple pathogenically relevant epitopes (2013) (2)
- A unique monoclonal antibody 29A stains the cytoplasm of amniotic epithelia and cutaneous basement membrane. (2006) (2)
- Calcinosis cutis in self‐healing dominant dystrophic epidermolysis bullosa (2020) (2)
- Collagen XVII deficiency alters epidermal patterning (2022) (2)
- Abnormalities of basal cell keratin in epidermolysis bullosa simplex do not affect the expression patterns of suprabasal keratins and cornified cell envelope proteins (1998) (2)
- CDK16/PCTK1/PCTAIRE1 is highly expressed in melanomas but not in melanocytic nevi or sarcomas (2019) (2)
- Positron emission tomography–computed tomography can be useful in the early detection of metastases in primary mucinous carcinoma of the skin on the head and neck (2015) (2)
- Mucosal substrates successfully identify the autoantigen in a case of mucous membrane pemphigoid (2018) (2)
- Late‐onset skin involvement on the forehead in multicentric Castleman disease (2017) (2)
- Complement fixation by Brazilian pemphigus foliaceus antibodies in vitro. (1986) (2)
- Usefulness of thermography techniques for evaluating the disease activity in Kimura’s disease (2008) (2)
- Speckled lentiginous nevus in a patient with Hermansky–Pudlak syndrome type 1 (2020) (2)
- Confluent and reticulated papillomatosis associated with 15q tetrasomy syndrome. (2013) (2)
- Occupational contact dermatitis caused by asparagus (2010) (2)
- Severe subcutaneous hematoma in a patient with psoriatic arthritis: Changes of platelet count in psoriatic patients with biologic agents (2017) (2)
- Sweet's Syndrome Mimicking Anti-Neutrophil Cytoplasmic Antibodies-Associated Vasculitis. (2018) (2)
- A case of recessive dystrophic epidermolysis bullosa with a novel c.6885_6898del14 mutation in the COL7A1 gene. (2017) (2)
- Generalized Pustular Psoriasis. (2017) (2)
- The First Case of Hereditary Fibrosing Poikiloderma with Tendon Contractures, Myopathy, and Pulmonary Fibrosis (POIKTMP) Who Showed Efficacy of Corticosteroids for Pulmonary Involvement (2020) (2)
- Recurrent course and CD30 expression of atypical T lymphocytes distinguish lymphomatoid papulosis from primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma. (2014) (2)
- Epidermolysis bullosa: diagnosis and therapy (2009) (2)
- Unusual post‐patch testing erythema: a late, granulomatous, non‐eczematous reaction to gold sodium thiosulphate (2018) (2)
- Fc‐binding proteins enhance autoantibody‐induced BP180 depletion in pemphigoid (2019) (2)
- Angiosarcoma on the lower abdominal wall associated with chronic lymphedema in an obese woman (2012) (2)
- Clinical and genetic analysis of Fabry disease: report of six cases including three heterozygous females. (2008) (2)
- Adjuvant therapy with low‐dose interferon‐beta for stage II and III melanoma: results of a retrospective analysis (2017) (2)
- Induction of macrophage migration inhibitory factor precedes the onset of acute tonsillitis. (2004) (2)
- Dermoscopic features of Bednar tumor: Report of a case (2018) (2)
- Vulvar basal cell carcinoma with adhesion of the labia majora and minora (2017) (2)
- Chronic papillomatous dermatitis around an ileostoma (2016) (2)
- Bowen's disease on the palm presents refractory skin erosion without erythematous plaque (2015) (2)
- Widespread keratosis follicularis squamosa (2009) (2)
- Chemiluminescent enzyme immunoassay failed to detect anti‐desmoglein 3 antibodies in a case of pemphigus vulgaris (2017) (2)
- Non‐Hodgkin lymphoma preceded by recalcitrant eczema (2007) (2)
- Infantile eczema caused by formula milk (2013) (2)
- Lethal junctional epidermolysis bullosa showing mild blister at birth (1999) (1)
- Bone marrow clonal T-cell population in lymphomatoid papulosis. (2005) (1)
- Case of peripheral T‐cell lymphoma, not otherwise specified, presenting dyshidrosis‐like eruptions as the first clinical manifestation (2017) (1)
- Case of bullous erythema ab igne mimicking localized bullous pemphigoid. (2020) (1)
- Collagen XVII participates in keratinocyte adhesion to collagen IV, and in p38-MAPK-dependent migration and cell signaling (2009) (1)
- A Nodular Lesion of the Foot Detected by 18F-FDG PET/CT in Mycosis Fungoides: A Plantar Wart. (2019) (1)
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- Keratinocyte lipid transporter ABCA12 is highly expressed In the late stages of human epidermal development (2006) (0)
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- Prevalent and Rare Filaggrin Mutations in Japanese Patients with Atopic Dermatitis (2008) (0)
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- Welcome all international dermatology researchers to the 34th Annual Meeting of the Japanese Society of Investigative Dermatology (JSID) and the JSID-Asia-Oceania-Forum on Hair Research and Stem Cells December 4-6, 2009, in Fukuoka City, Kyushu, Japan (2009) (0)
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- 158 Generation of junctional epidermolysis bullosa model mice with revertant mosaicism (2021) (0)
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- Instructions for use Title Possible role of endoplasmic reticulum stress in thepathogenesis of Darier ' s disease (2017) (0)
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- 198 Immunohistochemical features in the lesional skin of severe congenital ichthyosis (1995) (0)
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- Small diameter porous honeycomb substrates are more effective at cultivating human keratinocyte and dermal fibroblast cultures (2006) (0)
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- A novel frameshift mutation in a V2 domain of KRT1 causes ichthyosis hystrix Curth-Macklin type and may alter keratin organization (2013) (0)
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- Prevalent and rare filaggrin mutations in Japanese patients with ichthyosis vulgaris and atopic dermantitis (2008) (0)
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- Instructions for use Title A novel ABCA 12 mutation 3270 delT causes harlequin ichthyosis (2017) (0)
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- Several laminin subunits colocalize beneath hemidesmosomes in the human epidermal basement membrane zone (2003) (0)
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- Transglutaminase 1 in human hair follicle. (1999) (0)
- Cutaneous inflammatory myofibroblastic tumour: a case report and literature review (2017) (0)
- 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 (2017) (0)
- Kindlin-1 is important in human keratinocyte-substrate focal contact-mediated-adhesion, and cell survival/protection from apoptosis in vitro (2006) (0)
- Immunohistochemical, and morphological alterations in epidermal. Basement membrane in skin cancers study using cryofixed, freeze-dried and paraffin-embedded skin sections (1993) (0)
- Silicone medical adhesive removers for hyperkeratosis in epidermolysis bullosa (2016) (0)
- The expression of laminin 5 is concurrent with the assembly of hemidesmosomes in the developing human epidermal basement membrane (2004) (0)
- Isolation of mouse monoclonal antibodies reactive with maturation-related unique epitope(s) on human type VII collagen (2013) (0)
- Laminin 10 colocalizes with laminin 5 in the epidermal basement membrane zone beneath hemidesmosomes (2003) (0)
- The first familial cases of epidermolysis bullosa simplex, generalized severe with p.Asn176Ser in KRT5 revealing the clinical chronology (2017) (0)
- 011 Intravenous immunoglobulin reduces pathogenic antibodies, serum IL-6 levels and disease severity in experimental bullous pemphigoid (2018) (0)
- 583 Selective epidermal removal is a robust platform for understanding context-dependent epithelial cell activation (2019) (0)
- Ultrastructural localization of HMB-45 antigen in the fetal melanocytes and melanoma cells (1993) (0)
- [Localized scleroderma and PSS specific anti-Og antibody (author's transl)]. (1981) (0)
- Urticaria, prurigo, and pruritus (2016) (0)
- Pemphigoid Model Activation in Experimental Bullous Domain Induces Blisters via Complement Human Collagen 17 Noncollagenous 16A Human IgG1 Monoclonal Antibody against (2010) (0)
- 085 Type XVII collagen suppresses interfollicular epidermal proliferation in neonatal and aged skin, and helps rejuvenate epidermis (2017) (0)
- 358 Treg dysfunction leads to spontaneous production of autoantibodies to bullous pemphigoid antigens in mice (2017) (0)
- Unique ontogenic localization of possible stem cells of follicular epithelium in developing human hair follicle (1998) (0)
- Contents, Vol. 180, 1990 (1990) (0)
- 012 Treg dysfunction induces autoantibodies to type XVII collagen and BP230 in mice and humans (2018) (0)
- 368 Novel mevalonate kinase mutation in a patient with porokeratosis ptychotropica (2019) (0)
- A case of squamous cell carcinoma on the external genitalia in the oldest old: A struggle for the choice of appropriate therapy (2007) (0)
- DNA-based prenatal diagnosis of harlequin ichthyosis with residual ABCA12 expression (2006) (0)
- Basal Cell Carcinoma or Trichoblastoma ? Dermoscopic Examination of Black Macules Developing in the Same Nevus (2016) (0)
- Collagen XVII in hemidesmosomes is involved in keratinocyte-collagen IV adhesion and p38-MAPK-dependent cell migration and signaling (2009) (0)
- Monoclonal human IgG1 and IgG4 against COL17 induce skin fragility in neonatal COL17-humanized mice in a complement-independent manner (2013) (0)
- Double-negative T-cell Lymphoma : A Variant of Primary Cutaneous CD 8 + Aggressive Epidermotropic Cytotoxic T-cell Lymphoma ? (0)
- Expression of various epidermal basement membrane associated antigens in 36 Japanese patients with epidermolysis bullosa (1994) (0)
- A Case of Pulmonary Metastasis of Epithelioid Sarcoma Presenting as Pulmonary Cysts with CA 125 Expression (2017) (0)
- Minute reddish patch of extramammary Paget’s disease with notable lymph node metastases (2013) (0)
- 053 Novel mutations in the LAMB3 gene in two Japanese families with Herlitz junctional epidermolysis bullosa and their application for prenatal diagnosis (1997) (0)
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What Schools Are Affiliated With Hiroshi Shimizu?
Hiroshi Shimizu is affiliated with the following schools:
