- 21.
-
Nishizawa A, Nakano H, Satoh T, Takayama K, Sawamura D, Yokozeki H. Haber’s syndrome may be a clinical entity different from Dowling-Degos disease.
Br J Dermatol, 2008; 160(1): 215-217. - 20.
-
Nakano H, Akasaka E, Rokunohe D, Yokoyama S, Toyomaki Y, Umegaki N, Mitsuhashi Y, Sawamura D. A novel homozygous missense mutation in the fatty aldehyde dehydrogenase gene causes Sjogren-Larsson syndrome.
J Dermatol Sci 2008; 52(2): 136-138. - 19.
-
Kivisaari AK, Kallajoki M, Mirtti T, McGrath JA, Bauer JW, Weber F, Konigova R, Sawamura D, Sato-Matsumura KC, Shimizu H, Csikos M, Sinemus K, Beckert W, Kahari VM.Transformation-specific matrix metalloproteinases (MMP)-7 and MMP-13 are expressed by tumour cells in epidermolysis bullosa-associated squamous cell carcinomas.
Br J Dermatol 2008; 158(4): 778-85. - 18.
-
Nomura T, Kodama K, Moriuchi R, Yaosaka M, Kawasaki H, Abe M, Sawamura D, Shimizu H.Papuloerythroderma of Ofuji associated with early gastric cancer.
Int J Dermatol 2008; 47(6): 590-591. - 17.
-
Nishie W, Sawamura D, Iitoyo M, Shimizu H.Intravascular histiocytosis associated with rheumatoid arthritis.
Dermatology 2008; 217(2): 144-145. - 16.
-
Takiyoshi N, Nakano H, Kaneko T, Aizu T, Nakajima K, Akasaka E, Rokunohe D, Sawamura D. Multiple desmoplastic trichoepitheliomas with ossification and cholesterol deposition.
Exp Dermatol 2009; 34(5): 634-635. - 15.
-
Minakawa S, Nakajima K, Aizu T, Nomura K, Kaimori K, A case of zosteriform metastatic skin cancer.
Clin Exp Dermatol 2008; 33(6): 808-810. - 14.
-
Nagasaki A, Nishie W, Sato K, Oba I, Noguchi E, Akitsu H, Sawamura D, Shimizu H. Clinical and Genetic analysis of Fabry disease: report of 6 cases including 3 heterozygous females.
J Dermatol Sci 2008; 52(1): 61-64. - 13.
-
Yamamoto C, Tamai K, Nakano H, Matsuzaki Y, Kaneko T, Sawamura D. Vitamin D3 inhibits expression of pemphigus vulgaris antigen, desmoglein 3: implication of partial mechanism in pharmacological effect of VD3 on skin diseases.
Mol Med Rep 2008; 1: 581-583. - 12.
-
Kitamura H, Kaneko T, Nakano H, Terui H, Ito E, Sawamura D. Juvenile myelomonocytic leukemia presenting multiple painful erythematous lesions diagnosed as Sweet’s syndrome.
J Dermatol 2008; 35: 368-370. - 11.
-
Kakizaki I, Itano N, Kimata K, Hanada K, Kon A, Yamaguchi M, Takahashi T, Takagaki KFUp-regulation of hyaluronan synthase genes in cultured human epidermal keratinocytes by UVB irradiation.
Arch Biochem Biophys 2008; 471(1): 85-93. - 10.
-
Nanashima N, Akita M, Yamada T, Shimizu T, Nakano H, Fan Y, Tsuchida S.The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes.
J Biol Chem 2008; 283(24): 16868-16875. - 9.
-
Nishizawa A, Nakajima R, Nakano H, Sawamura D, Takayama K, Satoh T, Yokozeki H. A de novo missense mutation in the keratin 13 gene in oral white sponge nevus.
Br J Dermatol 2008; 159(4): 974-975. - 8.
-
Rokunohe A, Nakano H, Aizu T, Kaneko T, Nakajima K, Ikenaga S, Matsuzaki Y, Murai T, Tamai K, Sawamura D. Significance of sentinel node biopsy in the management of squamous cell carcinoma arising from recessive dystrophic epidermolysis bullosa.
J Dermatol 2008; 35(6): 336-340. - 7.
-
Aizu T, Tamai K, Nakano H, Rokunohe D, Toyomaki Y, Uitto J, Sawamura D. Calcineurin/NFAT-Dependent Regulation of 230-kD Bullous Pemphigoid Antigen (BPAG1) Gene Expression in Normal Human Epidermal Keratinocytes.
J Dermatol Sci 2008; 51(1): 45-51. - 6.
-
Nakajima K, Tamai K, Yamazaki T, Toyomaki Y, Nakano H, Uitto J, Sawamura D. Identification of Skn-1n, a splice variant that is induced by high calcium concentration and specifically expressed in normal human keratinocytes.
J Invest Dermatol 2008; 128(5): 1336-9. - 5.
-
Rokunohe D, Nakano H, Ikenaga S, Umegaki N, Kaneko T, Matsuhashi Y, Tandoh Y, Toyoki Y, Hakamada K, Kusumi T, Harada K, SawamuraD. Reduction in epidermal Langerhans cells in patients with necrolytic migratory erythema.
J Dermatol Sci 2008; 50(1): 76-80. - 4.
-
Nakajima K, Nakano H, Takiyoshi N, Rokunohe A, Ikenaga S, Aizu T, Kaneko T, Mitsuhashi Y, Sawamura D. Papillon-Lef?vre syndrome and malignant melanoma: a high incidence of melanoma development in Japanese palmoplantar keratoderma patients.
Dermatol 2008; 217(1): 58-62. - 3.
-
Sato-Jin K, Nishimura EK, Akasaka E, Huber W, Nakano H, Miller A, Du J, Wu M, Hanada K, Sawamura D, Fisher DE, and Imokawa G. Epistatic connections between MITF and endothelin signaling in Waardenburg syndrome and other pigmentary disorders.
FASEB J 2008; 22(4): 1155-68. - 2.
-
Hamada T, Fukuda S, Ishii N, Sakaguchi S, Ishikawa T, Abe T, Yasumoto S, Hashimoto T, Nakano H, Sawamura D. Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa: The splice site mutation c.6216+5G>T in the COL7A1 gene results in aberrant and normal splicings.
J Dermatol Sci 2008; 50(2): 147-50. - 1.
-
Yamamoto C, Tamai K, Nakano H, Matsuzaki Y, Kaneko T, Sawamura D. Vitamin D(3) inhibits expression of bullous pemphigoid antigen 1 through post-transcriptional mechanism without new protein synthesis.
J Dermatol Sci 2008; 50(2): 155-158.
