Usami S - Search Results

1

TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion.

Moteki H, Nishio SY, Hashimoto S, Takumi Y, Iwasaki S, Takeichi N, Fukuda S, Usami S. Moteki H, et al. Among authors: usami s. J Hum Genet. 2012 Sep;57(9):587-92. doi: 10.1038/jhg.2012.73. Epub 2012 Jun 21. J Hum Genet. 2012. PMID: 22718023

2

Cell death in the inner ear associated with aging is apoptosis?

Usami S, Takumi Y, Fujita S, Shinkawa H, Hosokawa M. Usami S, et al. Brain Res. 1997 Jan 30;747(1):147-50. doi: 10.1016/s0006-8993(96)01243-7. Brain Res. 1997. PMID: 9042539

3

Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.

Usami S, Abe S, Kasai M, Shinkawa H, Moeller B, Kenyon JB, Kimberling WJ. Usami S, et al. Laryngoscope. 1997 Apr;107(4):483-90. doi: 10.1097/00005537-199704000-00011. Laryngoscope. 1997. PMID: 9111378

4

Discrete cellular and subcellular localization of glutamine synthetase and the glutamate transporter GLAST in the rat vestibular end organ.

Takumi Y, Matsubara A, Danbolt NC, Laake JH, Storm-Mathisen J, Usami S, Shinkawa H, Ottersen OP. Takumi Y, et al. Among authors: usami s. Neuroscience. 1997 Aug;79(4):1137-44. doi: 10.1016/s0306-4522(97)00025-0. Neuroscience. 1997. PMID: 9219972

5

Sensorineural hearing loss caused by mitochondrial DNA mutations: special reference to the A1555G mutation.

Usami S, Abe S, Shinkawa H, Kimberling WJ. Usami S, et al. J Commun Disord. 1998 Sep-Oct;31(5):423-34; quiz 434-5. doi: 10.1016/s0021-9924(98)00014-8. J Commun Disord. 1998. PMID: 9777488 Review.

6

Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.

Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ. Abe S, et al. Among authors: usami s. Eur J Hum Genet. 1998 Nov-Dec;6(6):563-9. doi: 10.1038/sj.ejhg.5200239. Eur J Hum Genet. 1998. PMID: 9887373

7

Fluctuating sensorineural hearing loss associated with enlarged vestibular aqueduct maps to 7q31, the region containing the Pendred gene.

Abe S, Usami S, Hoover DM, Cohn E, Shinkawa H, Kimberling WJ. Abe S, et al. Among authors: usami s. Am J Med Genet. 1999 Feb 12;82(4):322-8. Am J Med Genet. 1999. PMID: 10051166

8

Immunoelectron microscopy of AMPA receptor subunits reveals three types of putative glutamatergic synapse in the rat vestibular end organs.

Matsubara A, Takumi Y, Nakagawa T, Usami S, Shinkawa H, Ottersen OP. Matsubara A, et al. Among authors: usami s. Brain Res. 1999 Feb 20;819(1-2):58-64. doi: 10.1016/s0006-8993(98)01345-6. Brain Res. 1999. PMID: 10082861

9

Quantitative immunogold cytochemistry reveals sources of glutamate release in inner ear ischemia.

Matsubara A, Kawabata Y, Takumi Y, Usami S, Shinkawa H, Haruta A, Matsuda K, Tono T. Matsubara A, et al. Among authors: usami s. Acta Otolaryngol Suppl. 1998;539:48-51. Acta Otolaryngol Suppl. 1998. PMID: 10095861

10

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations.

Usami S, Abe S, Weston MD, Shinkawa H, Van Camp G, Kimberling WJ. Usami S, et al. Hum Genet. 1999 Feb;104(2):188-92. doi: 10.1007/s004390050933. Hum Genet. 1999. PMID: 10190331

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