Hiroshi Shimizu

发表

Detection of Antigens by Immunofluorescence on Ultrathin Cryosections of Skin

T. Nishikawa, Y. Kurihara, T. Masunaga, 1998, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

Immunohistochemical, ultrastructural, and molecular features of Kindler syndrome distinguish it from dystrophic epidermolysis bullosa.

R. Burgeson, H. Shimizu, T. Nishikawa, 1997, Archives of dermatology.

Xanthoma striatum palmare as an early sign of familial type III hyperlipoproteinemia with an apoprotein E genotype ε2/ε2

H. Yokoshiki, K. Sato-Matsumura, T. Matsumura, 2003 .

Molecular basis of recessive dystrophic epidermolysis bullosa: genotype/phenotype correlation in a case of moderate clinical severity.

H. Shimizu, T. Nishikawa, J. Uitto, 1996, The Journal of investigative dermatology.

Gap junction development in the human fetal hair follicle and bulge region

J. R. McMillan, M. Akiyama, H. Shimizu, 2004, The British journal of dermatology.

Dystrophic form of inherited epidermolysis bullosa in a dog (Akita Inu)

H. Shimizu, T. Nishikawa, T. Masunaga, 1995, The British journal of dermatology.

Expression and ultrastructural localization of HMB‐45 antigen

T. Nishikawa, A. Kikuchi, Hiroshi Shimizu, 1996, British Journal of Dermatology.

Development of pemphigus vulgaris in a patient with pemphigus foliaceus: antidesmoglein antibody profile shift confirmed by enzyme-linked immunosorbent assay.

H. Shimizu, T. Nishikawa, M. Amagai, 2000, Journal of the American Academy of Dermatology.

Immunohistochemical and Ultrastructural Studies

M. Akiyama, H. Shimizu, T. Nishikawa, 1993, The American Journal of dermatopathology.

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?

H. Shimizu, J. McGrath, T. Hashimoto, 2000, The Journal of investigative dermatology.

Coexistence of psoriasis and an unusual IgG‐mediated subepidermal bullous dermatosis: identification of a novel 200‐kDa lower lamina lucida target antigen

H. Shimizu, T. Hashimoto, A. Ishiko, 1996, The British journal of dermatology.

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.

H. Shimizu, T. Nishikawa, Hayato Takahashi, 2000, The Journal of investigative dermatology.

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.

H. Shimizu, T. Saida, T. Nishikawa, 1998, The Journal of investigative dermatology.

Demonstration of intra- and extracellular localization of bullous pemphigoid antigen using cryofixation and freeze substitution for postembedding immunoelectron microscopy

H. Shimizu, R. Eady, A. Kennedy, 2004, Archives of Dermatological Research.

A novel subepidermal blistering disease with autoantibodies to a 200-kDa antigen of the basement membrane zone.

H. Shimizu, E. Bröcker, D. Zillikens, 1996, The Journal of investigative dermatology.

Delayed assembly of desmosomes in keratinocytes with disrupted classic-cadherin-mediated cell adhesion by a dominant negative mutant.

H. Shimizu, T. Nishikawa, M. Takeichi, 1995, The Journal of investigative dermatology.

Pemphigus vulgaris and pemphigus foliaceus sera show an inversely graded binding pattern to extracellular regions of desmosomes in different layers of human epidermis.

H. Shimizu, T. Nishikawa, T. Hashimoto, 1995, The Journal of investigative dermatology.

White fibrous papulosis of the neck: a new clinicopathologic entity?

H. Shimizu, T. Nishikawa, S. Kimura, 1989, Journal of the American Academy of Dermatology.

Dissociation of intra‐ and extracellular domainsof desmosomal cadherins and E‐cadherin inHailey–Hailey disease and Darier’s disease

M. Akiyama, H. Shimizu, T. Nishikawa, 2000, The British journal of dermatology.

Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy.

H. Shimizu, T. Nishikawa, J. Uitto, 1996, Human molecular genetics.

Unusual variants of pemphigoid: from pruritus to pemphigoid nodularis

N. Smith, M. Black, W. Griffiths, 1992, Journal of cutaneous pathology.

A novel subepidermal blistering disease with autoantibodies to a 200-kDa antigen of the basement membrane zone.

H. Shimizu, E. Bröcker, D. Zillikens, 1996, The Journal of investigative dermatology.

Pemphigus: from immunofluorescence to molecular biology.

H. Shimizu, T. Nishikawa, M. Amagai, 1996, Journal of dermatological science.

Autoantibodies from patients with cicatricial pemphigoid target different sites in epidermal basement membrane.

H. Shimizu, T. Nishikawa, K. Yancey, 1995, The Journal of investigative dermatology.

A case of linear IgA buUous dermatosis with IgA anti‐type VII collagen autoantibodies

H. Shimizu, T. Nishikawa, T. Hashimoto, 1996, The British journal of dermatology.

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.

H. Shimizu, T. Nishikawa, K. Yancey, 1998, The Journal of investigative dermatology.

Most anchoring fibrils in human skin originate and terminate in the lamina densa.

H. Shimizu, T. Nishikawa, L. Bruckner-Tuderman, 1997, Laboratory investigation; a journal of technical methods and pathology.

A case of bullous pemphigoid with antidesmoplakin autoantibodies

H. Shimizu, T. Nishikawa, T. Hashimoto, 1994, The British journal of dermatology.

Polymorphism in the tumor necrosis factor B gene is associated with Palmoplantar pustulosis.

H. Shimizu, T. Nishikawa, K. Hashigucci, 1999, Tissue antigens.