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Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) miceRAPHAEL, Yehoash; KOBAYASHI, Karen N; DOOTZ, Gary A et al.Hearing research. 2001, Vol 151, Num 1-2, pp 237-249, issn 0378-5955Article

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Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationBEN-YOSEF, Tamar; BELYANTSEVA, Inna A; RASMUSSEN, Julia et al.Human molecular genetics (Print). 2003, Vol 12, Num 16, pp 2049-2061, issn 0964-6906, 13 p.Article

Characterization of two transgene insertional mutations at pirouette, a mouse deafness locusODEH, Hana; HAGIWARA, Nobuko; KOHRMAN, David C et al.Audiology & neuro-otology. 2004, Vol 9, Num 5, pp 303-314, issn 1420-3030, 12 p.Article

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Electromotile hearing : Acoustic tones mask psychophysical response to high-frequency electrical stimulation of intact guinea pig cochleaeLE PRELL, Colleen G; KAWAMOTO, Kohei; RAPHAEL, Yehoash et al.The Journal of the Acoustical Society of America. 2006, Vol 120, Num 6, pp 3889-3900, issn 0001-4966, 12 p.Article

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Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereociliaKAROLYI, I. Jill; PROBST, Frank J; RAPHAEL, Yehoash et al.Human molecular genetics (Print). 2003, Vol 12, Num 21, pp 2797-2805, issn 0964-6906, 9 p.Article

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6MITCHEM, Kristina L; HIBBARD, Ellen; BEYER, Lisa A et al.Human molecular genetics (Print). 2002, Vol 11, Num 16, pp 1887-1898, issn 0964-6906Article