|
Chen, Kejian; Godfrey, Donald A; Ilyas, Omer et al. (2009) Cerebellum-related characteristics of Scn8a-mutant mice. Cerebellum 8:192-201
|
|
Mustapha, Mirna; Beyer, Lisa A; Izumikawa, Masahiko et al. (2007) Whirler mutant hair cells have less severe pathology than shaker 2 or double mutants. J Assoc Res Otolaryngol 8:329-37
|
|
Cho, Younsook; Gong, Tzy-Wen L; Kanicki, Ariane et al. (2004) Noise overstimulation induces immediate early genes in the rat cochlea. Brain Res Mol Brain Res 130:134-48
|
|
Gong, Tzy-Wen L; Huang, Li; Warner, Steven J et al. (2003) Characterization of the human UBE3B gene: structure, expression, evolution, and alternative splicing. Genomics 82:143-52
|
|
Karolyi, I Jill; Probst, Frank J; Beyer, Lisa et al. (2003) Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia. Hum Mol Genet 12:2797-805
|
|
Cho, Younsook; Gong, Tzy-Wen L; Stover, Timo et al. (2002) Gene expression profiles of the rat cochlea, cochlear nucleus, and inferior colliculus. J Assoc Res Otolaryngol 3:54-67
|
|
Mitchem, Kristina L; Hibbard, Ellen; Beyer, Lisa A et al. (2002) Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6. Hum Mol Genet 11:1887-98
|
|
Stover, T; Nam, Y; Gong, T L et al. (2001) Glial cell line-derived neurotrophic factor (GDNF) and its receptor complex are expressed in the auditory nerve of the mature rat cochlea. Hear Res 155:143-51
|
|
Bespalova, I N; Van Camp, G; Bom, S J et al. (2001) Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Hum Mol Genet 10:2501-8
|
|
Chung, J W; Schacht, J (2001) ATP and nitric oxide modulate intracellular calcium in isolated pillar cells of the guinea pig cochlea. J Assoc Res Otolaryngol 2:399-407
|
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