Shin-Ichi Usami
Department of Otorhinolaryngology
Shinshu University School of Medicine
Asahi
Matsumoto
Japan
[email]@hsp.md.shinshu-u.ac.jp
Name/email consistency: high
- The responsible genes in Japanese deafness patients and clinical application using Invader assay. Usami, S., Wagatsuma, M., Fukuoka, H., Suzuki, H., Tsukada, K., Nishio, S., Takumi, Y., Abe, S. Acta Otolaryngol. (2008)
- The localization of proteins encoded by CRYM, KIAA1199, UBA52, COL9A3, and COL9A1, genes highly expressed in the cochlea. Usami, S., Takumi, Y., Suzuki, N., Oguchi, T., Oshima, A., Suzuki, H., Kitoh, R., Abe, S., Sasaki, A., Matsubara, A. Neuroscience (2008)
- Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease. Usami, S., Takahashi, K., Yuge, I., Ohtsuka, A., Namba, A., Abe, S., Fransen, E., Patthy, L., Otting, G., Van Camp, G. Eur. J. Hum. Genet. (2003)
- Molecular diagnosis of deafness: impact of gene identification. Usami, S., Koda, E., Tsukamoto, K., Otsuka, A., Yuge, I., Asamura, K., Abe, S., Akita, J., Namba, A. Audiol. Neurootol. (2002)
- Endoscopic-assisted myringoplasty. Usami, S., Iijima, N., Fujita, S., Takumi, Y. ORL J. Otorhinolaryngol. Relat. Spec. (2001)
- Neurotransmission in the vestibular endorgans--glutamatergic transmission in the afferent synapses of hair cells. Usami, S.I., Takumi, Y., Matsubara, A., Fujita, S., Ottersen, O.P. Biol. Sci. Space (2001)
- Sensorineural hearing loss associated with the mitochondrial mutations. Usami, S., Abe, S., Akita, J., Shinkawa, H., Kimberling, W.J. Adv. Otorhinolaryngol. (2000)
- Rapid mass screening method and counseling for the 1555A-->G mitochondrial mutation. Usami, S., Abe, S., Shinkawa, H., Inoue, Y., Yamaguchi, T. J. Hum. Genet. (1999)
