Beyer LA - Search Results

1

Impaired intracellular signal transduction in gastric smooth muscle of diabetic BB/W rats.

Takahashi T, Kojima Y, Tsunoda Y, Beyer LA, Kamijo M, Sima AA, Owyang C. Takahashi T, et al. Among authors: beyer la. Am J Physiol. 1996 Mar;270(3 Pt 1):G411-7. doi: 10.1152/ajpgi.1996.270.3.G411. Am J Physiol. 1996. PMID: 8638706

2

Severe vestibular and auditory impairment in three alleles of Ames waltzer (av) mice.

Raphael Y, Kobayashi KN, Dootz GA, Beyer LA, Dolan DF, Burmeister M. Raphael Y, et al. Among authors: beyer la. Hear Res. 2001 Jan;151(1-2):237-249. doi: 10.1016/s0378-5955(00)00233-1. Hear Res. 2001. PMID: 11124469

3

Morphological and physiological effects of long duration infusion of strychnine into the organ of Corti.

Dolan DF, Yamasoba T, Leonova E, Beyer LA, Raphael Y. Dolan DF, et al. Among authors: beyer la. J Neurocytol. 1999 Mar;28(3):197-206. doi: 10.1023/a:1007071905824. J Neurocytol. 1999. PMID: 10617902 Free article.

4

Hair cells in the inner ear of the pirouette and shaker 2 mutant mice.

Beyer LA, Odeh H, Probst FJ, Lambert EH, Dolan DF, Camper SA, Kohrman DC, Raphael Y. Beyer LA, et al. J Neurocytol. 2000 Apr;29(4):227-40. doi: 10.1023/a:1026515619443. J Neurocytol. 2000. PMID: 11276175 Free article.

5

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.

Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC. Mitchem KL, et al. Among authors: beyer la. Hum Mol Genet. 2002 Aug 1;11(16):1887-98. doi: 10.1093/hmg/11.16.1887. Hum Mol Genet. 2002. PMID: 12140191

6

Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degeneration.

Ben-Yosef T, Belyantseva IA, Saunders TL, Hughes ED, Kawamoto K, Van Itallie CM, Beyer LA, Halsey K, Gardner DJ, Wilcox ER, Rasmussen J, Anderson JM, Dolan DF, Forge A, Raphael Y, Camper SA, Friedman TB. Ben-Yosef T, et al. Among authors: beyer la. Hum Mol Genet. 2003 Aug 15;12(16):2049-61. doi: 10.1093/hmg/ddg210. Hum Mol Genet. 2003. PMID: 12913076

7

Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.

Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Karolyi IJ, et al. Hum Mol Genet. 2003 Nov 1;12(21):2797-805. doi: 10.1093/hmg/ddg308. Epub 2003 Sep 9. Hum Mol Genet. 2003. PMID: 12966030

8

Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus.

Odeh H, Hagiwara N, Skynner M, Mitchem KL, Beyer LA, Allen ND, Brilliant MH, Lebart MC, Dolan DF, Raphael Y, Kohrman DC. Odeh H, et al. Among authors: beyer la. Audiol Neurootol. 2004 Sep-Oct;9(5):303-14. doi: 10.1159/000080701. Epub 2004 Sep 3. Audiol Neurootol. 2004. PMID: 15347914

9

Chronic excitotoxicity in the guinea pig cochlea induces temporary functional deficits without disrupting otoacoustic emissions.

Le Prell CG, Yagi M, Kawamoto K, Beyer LA, Atkin G, Raphael Y, Dolan DF, Bledsoe SC Jr, Moody DB. Le Prell CG, et al. Among authors: beyer la. J Acoust Soc Am. 2004 Aug;116(2):1044-56. doi: 10.1121/1.1772395. J Acoust Soc Am. 2004. PMID: 15376671

10

p27(Kip1) deficiency causes organ of Corti pathology and hearing loss.

Kanzaki S, Beyer LA, Swiderski DL, Izumikawa M, Stöver T, Kawamoto K, Raphael Y. Kanzaki S, et al. Among authors: beyer la. Hear Res. 2006 Apr;214(1-2):28-36. doi: 10.1016/j.heares.2006.01.014. Epub 2006 Mar 2. Hear Res. 2006. PMID: 16513305

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