Tomiya Yasushi | Department Of Dermatology Nagoya University Graduate School Of Medicine

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概要

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著作論文

Dyschromatosis symmetrica hereditaria associated with neurological disorders
Investigation of the IVS5 +5G → A splice site mutation of HPS1 gene found in Japanese patients with Hermansky-Pudlak syndrome
Characterization of the human RAB38 and RAB7 genes : exclusion of new major pathological loci for Japanese OCA
EVALUATION OF CETIRIZINE HYDROCHLORIDE BASED FOR CHRONIC URTICARIA
Interval sentinel lymph nodes in patients with cutaneous melanoma : A single-institution study in Japan
Four novel mutations of the ADAR1 gene in dyschromatosis symmetrica hereditaria
Two novel mutations detected in Japanese patients with oculocutaneous albinism
Establishment of tyrosinase sequence database in normally pigmented Indians and Japanese for rapid determination of novel mutations
Detection of various types of human papillomavirus DNA, mainly belonging to the cutaneous-group, more frequently in normal tissue than in squamous cell carcinomas of the lip
A novel mutation of the tyrosinase gene causing oculocutaneous albinism type 1 (OCA1)
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
Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9
R278TER and P431L mutations of the tyrosinase gene exist in Japanese patients with tyrosinase-negative oculocutaneous albinism
Dermoscopic evaluation of vascular structure of various skin tumors in Japanese patients
Six novel mutations of the ADAR1 gene in patients with dyschromatosis symmetrica hereditaria : Histological observation and comparison of genotypes and clinical phenotypes
Mutation analyses of patients with dyschromatosis symmetrica hereditaria : Five novel mutations of the ADAR1 gene

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