Masae Okura
Sapporo, Japan
Last Updated: 09/26/2026
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Found 31 publications
Fusion Gene Detection in Driver Mutation-Negative Melanomas Using RNA-Based Anchored Multiplex Polymerase Chain Reaction.
Journal: Pigment cell & melanoma research
Published: January 09, 2025
Dominant inheritance in hereditary angioedema associated with carboxypeptidase N deficiency.
Journal: Allergology international : official journal of the Japanese Society of Allergology
Published: November 24, 2024
A case of familial progressive hyperpigmentation with or without hypopigmentation presenting with hypopigmented striae along the lines of Blaschko.
Journal: The Journal of dermatology
Published: May 17, 2024
Mosaic SUFU mutation associated with a mild phenotype of multiple hereditary infundibulocystic basal cell carcinoma syndrome.
Journal: The Journal of dermatology
Published: April 05, 2024
Genetic Characteristics of Cutaneous, Acral, and Mucosal Melanoma in Japan.
Journal: Cancer medicine
Published: January 30, 2024
Significant and Various Effects of ML329-Induced MITF Suppression in the Melanoma Cell Line.
Journal: Cancers
Published: December 06, 2023
Effects of temozolomide on tumor mutation burden and microsatellite instability in melanoma cells.
Journal: The Journal of dermatology
Published: June 23, 2023
A Japanese patient with hereditary angioedema caused by deep intron variation in the SERPING1 gene.
Journal: The Journal of dermatology
Published: January 31, 2023
Genetic analyses of a secondary poroma and trichoblastoma in a HRAS-mutated sebaceous nevus.
Journal: The Journal of dermatology
Published: January 28, 2021
Neurofibromatosis type 1 without cutaneous neurofibromas: a rare genotype-phenotype correlation?
Journal: European journal of dermatology : EJD
Published: November 13, 2020
Homozygous promoter variant of SLC45A2 causes diverse hair color and patterns.
Journal: The Journal of dermatology
Published: July 21, 2020
Last Updated: 09/26/2026