Kelly N. Owens

Affiliations: 
Biological Structure University of Washington, Seattle, Seattle, WA 
Area:
hearing and genetics
Google:
"Kelly Owens"
Mean distance: 13.65 (cluster 6)
 
SNBCP
Cross-listing: FlyTree

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Publications

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Chowdhury S, Owens KN, Herr RJ, et al. (2017) Phenotypic Optimization of Urea-Thiophene Carboxamides to Yield Potent, Well Tolerated and Orally Active Protective Agents Against Aminoglycoside-Induced Hearing Loss. Journal of Medicinal Chemistry
Stawicki TM, Hernandez L, Esterberg R, et al. (2016) Cilia-Associated Genes Play Differing Roles in Aminoglycoside-Induced Hair Cell Death in Zebrafish. G3 (Bethesda, Md.)
Stawicki TM, Owens KN, Linbo T, et al. (2014) The zebrafish merovingian mutant reveals a role for pH regulation in hair cell toxicity and function. Disease Models & Mechanisms. 7: 847-56
Hailey DW, Roberts B, Owens KN, et al. (2012) Loss of Slc4a1b chloride/bicarbonate exchanger function protects mechanosensory hair cells from aminoglycoside damage in the zebrafish mutant persephone. Plos Genetics. 8: e1002971
Vlasits AL, Simon JA, Raible DW, et al. (2012) Screen of FDA-approved drug library reveals compounds that protect hair cells from aminoglycosides and cisplatin. Hearing Research. 294: 153-65
Namdaran P, Reinhart KE, Owens KN, et al. (2012) Identification of modulators of hair cell regeneration in the zebrafish lateral line. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 3516-28
Coffin AB, Ou H, Owens KN, et al. (2010) Chemical screening for hair cell loss and protection in the zebrafish lateral line. Zebrafish. 7: 3-11
Coffin AB, Reinhart KE, Owens KN, et al. (2009) Extracellular divalent cations modulate aminoglycoside-induced hair cell death in the zebrafish lateral line. Hearing Research. 253: 42-51
Owens KN, Coffin AB, Hong LS, et al. (2009) Response of mechanosensory hair cells of the zebrafish lateral line to aminoglycosides reveals distinct cell death pathways. Hearing Research. 253: 32-41
Gorden NT, Arts HH, Parisi MA, et al. (2008) CC2D2A is mutated in Joubert syndrome and interacts with the ciliopathy-associated basal body protein CEP290. American Journal of Human Genetics. 83: 559-71
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