Tomita Y | Department Of Dermatology Nagoya University Graduate School Of Medicine

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概要

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著作論文

Genotyping of Candida albicans by Fragment Analysis of Microsatellites Combined with 25S rDNA and RPS-based Strategies
Epidemiological study of Candida species in cutaneous candidiasis based on PCR using a primer mix specific for the DNA topoisomerase II gene
PCR and PCR-RFLP techniques targeting the DNA topoisomerase II gene for rapid clinical diagnosis of the etiologic agent of dermatophytosis
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
Genotype analysis of Candida albicans isolates obtained from different body locations of patients with superficial candidiasis using PCRs targeting 25S rDNA and ALT repeat sequences of the RPS
Genotyping of Candida albicans on the basis of polymorphisms of ALT repeats in the repetitive sequence (RPS)
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
Effects of topical vehicles on growth of the lipophilic Malassezia species
Antigenic components of Malassezia species for immunoglobulin E antibodies in sera of patients with atopic dermatitis
Isolation and Characterization of a Major Antigenic Component of Malassezia globosa to IgE Antibodies in Sera of Patients with Atopic Dermatitis
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
Oculocutaneous Albinism and Analysis of Tyrosinase Gene in Japanese Patients
Mutation analyses of patients with dyschromatosis symmetrica hereditaria : Five novel mutations of the ADAR1 gene
Microsatellite-based Genotyping of Candida albicans Isolated from Patients with Superficial Candidiasis

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