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Journal of Leukocyte Biology|May 2, 2009
Pivotal Advance: Eosinophilia in the MES rat strain is caused by a loss-of-function mutation in the gene for cytochrome b(-245), alpha polypeptide (Cyba)Masayuki Mori, Guixin Li, Maiko Hashimoto, et al.
Clinical Case Reports|January 25, 2021
Cochlear implantation in a patient with a POU4F3 mutationKeitaro Miyake, Kyoko Shirai, Nobuhiro Nishiyama, et al.
Audiology & Neuro-Otology|June 8, 2002
Molecular diagnosis of deafness: impact of gene identificationShin-ichi Usami, Eiko Koda, Koji Tsukamoto, et al.
Brain Research. Molecular Brain Research|December 14, 2002
Microtubule associated protein (MAP1A) mRNA was up-regulated by hypergravity in the rat inner earYutaka Takumi, Naoya Iijima, Nobuyoshi Suzuki, et al.
Human Genetics|February 1, 2003
GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutationAkihiro Ohtsuka, Isamu Yuge, Shinobu Kimura, et al.
Acta Oto-Laryngologica|April 14, 2009
Semi-quantitative evaluation of endolymphatic hydrops by bilateral intratympanic gadolinium-based contrast agent (GBCA) administration with MRI for Meniere's diseaseHisakuni Fukuoka, Keita Tsukada, Maiko Miyagawa, et al.
Acta Oto-Laryngologica|October 30, 2009
Endolymphatic hydrops and therapeutic effects are visualized in 'atypical' Meniere's diseaseMaiko Miyagawa, Hisakuni Fukuoka, Keita Tsukada, et al.
Plos One|October 21, 2014
Gene expression pattern after insertion of dexamethasone-eluting electrode into the guinea pig cochleaYutaka Takumi, Shin-ya Nishio, Kenneth Mugridge, et al.
BMC Medical Genetics|October 13, 2011
Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutationHideki Mutai, Hiroko Kouike, Eiko Teruya, et al.
Acta Oto-Laryngologica|March 25, 2017
The clinical features and prognosis of mumps-associated hearing loss: a retrospective, multi-institutional investigation in JapanShinya Morita, Keishi Fujiwara, Atsushi Fukuda, et al.
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