Aki Oshima

Clinical features of patients with GJB2 (connexin 26) mutations: severity of hearing loss is correlated with genotypes and protein expression patterns

Tomohiro Oguchi, Akihiro Ohtsuka, Shigenari Hashimoto et al. · Journal of Human Genetics · 2005 · 89 citations · Full text

Genetic Disorder, Genetics, Audiology +9

Mutation profile of theCDH23 gene in 56 probands with Usher syndrome type I

Aki Oshima, Teresa Jaijo, Elena Aller et al. · Human Mutation · 2008 · 64 citations · Full text

Thecdh23 Gene, Congenital Deafness, Developmental Biology +14

Clinical characteristics and genotype–phenotype correlation of hearing loss patients with<i>SLC26A4</i>mutations

Hiroaki Suzuki, Aki Oshima, Koji Tsukamoto et al. · Acta Oto-Laryngologica · 2007 · 64 citations

μ-Crystallin as an Intracellular 3,5,3′-Triiodothyronine Holder in Vivo

Satoru Suzuki, Nobuyoshi Suzuki, Jun-ichirou Mori et al. · Molecular Endocrinology · 2007 · 59 citations · Full text

The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochlea

Shin‐ichi Usami, Yutaka Takumi, Naoki Suzuki et al. · Neuroscience · 2008 · 32 citations

Natural Sciences, Signal Recognition, Molecular Biology +7