KONO Michihiro | 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
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
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
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
Establishment of a Screening System for Chemicals that Upregulate a Melanoma Antigen, Melan-A/MART-1

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