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Rugsaseel, S
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Abe, S
Usami, S
Hoover, DM
Cohn, E
Shinkawa, H
Kimberling, WJ
Citation: S. Abe et al., Fluctuating sensorineural hearing loss associated with enlarged vestibularaqueduct maps to 7q31, the region containing the Pendred gene, AM J MED G, 82(4), 1999, pp. 322-328
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Hiramatsu, S
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Citation: S. Hiramatsu et al., Expression of a chitinase gene and lysis of the host cell wall during Chlorella virus CVK2 infection, VIROLOGY, 260(2), 1999, pp. 308-315
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Murayama, Y
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Citation: Y. Murayama et al., Transvenous Doppler guidewire sonographic monitoring during treatment of acomplex vertebral arteriovenous fistula associated with neurofibromatosis Type 1, NEURORADIOL, 41(5), 1999, pp. 328-333
Citation: Yl. Chang et al., Effects of palmatine on isometric force and intracellular calcium levels of arterial smooth muscle, LIFE SCI, 64(8), 1999, pp. 597-606
Authors:
Matsubara, A
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Nakagawa, T
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Citation: A. Matsubara et al., Immunoelectron microscopy of AMPA receptor subunits reveals three types ofputative glutamatergic synapse in the rat vestibular end organs, BRAIN RES, 819(1-2), 1999, pp. 58-64
Authors:
Kim, YD
Choi, W
Wakimoto, H
Usami, S
Tomokage, H
Ando, T
Citation: Yd. Kim et al., Direct observation of electron emission site on boron-doped polycrystalline diamond thin films using an ultra-high-vacuum scanning tunneling microscope, APPL PHYS L, 75(20), 1999, pp. 3219-3221
Authors:
Abe, S
Usami, S
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Weston, MD
Overbeck, LD
Hoover, DM
Kenyon, JB
Horai, S
Kimberling, WJ
Citation: S. Abe et al., Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation, EUR J HUM G, 6(6), 1998, pp. 563-569
Authors:
Takumi, Y
Nagelhus, EA
Eidet, J
Matsubara, A
Usami, S
Shinkawa, H
Nielsen, S
Ottersen, OP
Citation: Y. Takumi et al., Select types of supporting cell in the inner ear express aquaporin-4 waterchannel protein, EUR J NEURO, 10(12), 1998, pp. 3584-3595
Authors:
Tono, T
Ushisako, Y
Kiyomizu, K
Usami, S
Abe, S
Shinkawa, H
Komune, S
Citation: T. Tono et al., Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial mutation, AM J OTOL, 19(6), 1998, pp. 754-757