Výsledky vyhledávání - "Hiroshi Hachisuka"

Cultured keratinocytes from plectin/HD1-deficient epidermolysis bullosa simplex showed altered ability of adhesion to the matrix

Autor: Hiroshi Hachisuka, Koichiro Kurose, Katsushi Owaribe, Takashi Hashimoto, Osamu Mori, Hiroshi Shimizu

Publikováno v: Journal of Dermatological Science. 24:184-189

Epidermolysis bullosa simplex associated with late onset of muscular dystrophy has been found to show defective expression of plectin, an intracytoplasmic protein in hemidesmosomes. In this report, we examined ability of cell-to-matrix attachment of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f0f39ebdc249e21b10e55526de361c7
https://doi.org/10.1016/s0923-1811(00)00100-6

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Epidermolysis bullosa simplex associated with muscular dystrophy: Phenotype-genotype correlations and review of the literature

Autor: Hiroshi Hachisuka, Takeji Nishikawa, Hiroshi Shimizu, Jouni Uitto, Yasuko Takizawa, Masako Udono, Mitsuru Kawai, Satoru Murata, Leena Pulkkinen

Publikováno v: Journal of the American Academy of Dermatology. 41:950-956

Background: Epidermolysis bullosa simplex associated with muscular dystrophy (EBS-MD; OMIM# 226670) is an autosomal recessive disorder caused by genetic defects in the plectin gene. Because EBS-MD is relatively rare, and gene defects have been elucid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a186dbfaf9ac52a3d4f5063e6182a65
https://doi.org/10.1016/s0190-9622(99)70252-5

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Cameo

Autor: Hiroshi Hachisuka, Masahiro Kusuhara

Publikováno v: International Journal of Dermatology. 36:684-688

A 67-year-old Japanese man had been treated occasionally for asthma by oral administration of prednisolone at a dose between 5 and 15 mg/day for 18 years. In December 1993, the patient had a severe asthma attack, during which he developed a pneumotho

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bd4b5cedd71062d764e045ee4dd18d5a
https://doi.org/10.1046/j.1365-4362.1997.00287.x

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

Autor: Hiroshi Hachisuka, W.H. Irwin McLean, Hideo Yaoita, Takeji Nishikawa, Satoru Murata, Hiroshi Shimizu, Frances J.D. Smith, Leena Pulkkinen, Jouni Uitto

Publikováno v: Scopus-Elsevier

In a distinct autosomal recessive variant of epidermolysis bullosa, EB-MD, life-long skin blistering is associated with late-onset muscular dystrophy of unknown etiology. Electron microscopy of these patients' skin suggests that tissue separation occ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c4ef1a9f268ae5b3d5dd6b8f22bf14
https://doi.org/10.1093/hmg/5.10.1539

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Keratin 14 gene point mutation in the K�bner and Dowling-Meara types of epidermolysis bullosa simplex as detected by the PASA method

Autor: Hiroshi Hachisuka, Tadashi Karashima, Yoichiro Sasai, Mihoko Morita

Publikováno v: Archives of Dermatological Research. 287:142-145

Recent advances in molecular biology have enabled the association of epidermolysis bullosa simplex (EBS) with point mutations of keratin 14 and/or keratin 5 genes to be established. We describe here the detection of point mutations in genomic DNA fro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f03c421f50d68eb5388814cc8bec61eb
https://doi.org/10.1007/bf01262322

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A flow cytometric analysis of the DNA content of Paget cells in the epidermis and the tumor of extramammary Paget's disease

Autor: Yasuhiko Maeyama, Yoichiro Sasai, Hiroshi Hachisuka, Osamu Mori

Publikováno v: Acta Histochemica. 97:99-104

Summary In the present study, we have examined whether or not the Paget cells in cases with dermal invasion or metastasis exhibit a different DNA distribution pattern to that seen in the epidermis in extramammary Paget's disease. The DNA contents of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce0bbf68ad3a66b22b4728cc48a22576
https://doi.org/10.1016/s0065-1281(11)80210-2

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Bullous pemphigoid in a 19-year-old woman. A case with unusual target antigens

Autor: S. Fujiwara, Hiroshi Hachisuka, Masahiro Kusuhara, Yoichiro Sasai, Osamu Mori

Publikováno v: British Journal of Dermatology. 130:241-245

Summary We report a 19-year-old woman with typical clinical histological and immunofluorescence features of bullous pemphigoid. By immunoblotting, the serum was shown to detect antigens at 240 and 138 kDa. Elevated serum IgK levels were present, and

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6f65bec22ee01dab604a269a80bce58
https://doi.org/10.1111/j.1365-2133.1994.tb02909.x

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