Mitsuru Hattori
Nagasaki, 8528523, Japan
Last Updated: 09/26/2026
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Found 19 publications
Field survey of ticks following cases of severe fever with thrombocytopenia syndrome in companion animals in Japan.
Journal: Ticks and tick-borne diseases
Published: February 16, 2026
National Distribution of Bisexual and Parthenogenetic Haemaphysalis longicornis of Japan, and a Real-Time PCR-Based Method to Distinguish the Two Reproductive Groups.
Journal: Journal of parasitology research
Published: January 04, 2026
Emerging Multi-Source Transmission of SFTS Virus on a Remote Japanese Island: A One-Health Perspective.
Journal: International journal of molecular sciences
Published: January 03, 2026
Positive geographic correlation between soldiers' weapon size and defensive prowess in a eusocial aphid, Ceratovacuna japonica.
Journal: Scientific reports
Published: June 15, 2022
Intraspecific convergence of floral size correlates with pollinator size on different mountains: a case study of a bumblebee-pollinated Lamium (Lamiaceae) flowers in Japan.
Journal: BMC ecology and evolution
Published: January 28, 2021
Seasonal Migration in the Aphid Genus Stomaphis (Hemiptera: Aphididae): Discovery of Host Alternation Between Woody Plants in Subfamily Lachninae.
Journal: Journal of insect science (Online)
Published: June 23, 2020
Evolutionary diversification of Japanese Stomaphis aphids (Aphididae, Lachninae) in relation to their host plant use and ant association.
Journal: Die Naturwissenschaften
Published: November 07, 2019
Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review.
Journal: The Annals of otology, rhinology, and laryngology
Published: May 23, 2015
Gene expression profiles of the cochlea and vestibular endorgans: localization and function of genes causing deafness.
Journal: The Annals of otology, rhinology, and laryngology
Published: March 28, 2015
Mutations in the MYO15A gene are a significant cause of nonsyndromic hearing loss: massively parallel DNA sequencing-based analysis.
Journal: The Annals of otology, rhinology, and laryngology
Published: March 21, 2015
Hearing loss caused by a P2RX2 mutation identified in a MELAS family with a coexisting mitochondrial 3243AG mutation.
Journal: The Annals of otology, rhinology, and laryngology
Published: March 20, 2015
Last Updated: 09/26/2026