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2,316 results

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A catechol-O-methyltransferase that is essential for auditory function in mice and humans.
Du X, Schwander M, Moresco EM, Viviani P, Haller C, Hildebrand MS, Pak K, Tarantino L, Roberts A, Richardson H, Koob G, Najmabadi H, Ryan AF, Smith RJ, Müller U, Beutler B. Du X, et al. Among authors: smith rj. Proc Natl Acad Sci U S A. 2008 Sep 23;105(38):14609-14. doi: 10.1073/pnas.0807219105. Epub 2008 Sep 15. Proc Natl Acad Sci U S A. 2008. PMID: 18794526 Free PMC article.
Characterisation of DRASIC in the mouse inner ear.
Hildebrand MS, de Silva MG, Klockars T, Rose E, Price M, Smith RJ, McGuirt WT, Christopoulos H, Petit C, Dahl HH. Hildebrand MS, et al. Among authors: smith rj. Hear Res. 2004 Apr;190(1-2):149-60. doi: 10.1016/S0378-5955(04)00015-2. Hear Res. 2004. PMID: 15051137
Gene expression profiling analysis of the inner ear.
Hildebrand MS, de Silva MG, Klockars T, Campbell CA, Smith RJ, Dahl HH. Hildebrand MS, et al. Among authors: smith rj. Hear Res. 2007 Mar;225(1-2):1-10. doi: 10.1016/j.heares.2007.01.015. Epub 2007 Jan 18. Hear Res. 2007. PMID: 17300888 Review.
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function.
Schwander M, Sczaniecka A, Grillet N, Bailey JS, Avenarius M, Najmabadi H, Steffy BM, Federe GC, Lagler EA, Banan R, Hice R, Grabowski-Boase L, Keithley EM, Ryan AF, Housley GD, Wiltshire T, Smith RJ, Tarantino LM, Müller U. Schwander M, et al. Among authors: smith rj. J Neurosci. 2007 Feb 28;27(9):2163-75. doi: 10.1523/JNEUROSCI.4975-06.2007. J Neurosci. 2007. PMID: 17329413 Free PMC article.
Clinical aspects of hereditary hearing loss.
Kochhar A, Hildebrand MS, Smith RJ. Kochhar A, et al. Among authors: smith rj. Genet Med. 2007 Jul;9(7):393-408. doi: 10.1097/gim.0b013e3180980bd0. Genet Med. 2007. PMID: 17666886 Free article. Review.
Advances in molecular and cellular therapies for hearing loss.
Hildebrand MS, Newton SS, Gubbels SP, Sheffield AM, Kochhar A, de Silva MG, Dahl HH, Rose SD, Behlke MA, Smith RJ. Hildebrand MS, et al. Among authors: smith rj. Mol Ther. 2008 Feb;16(2):224-36. doi: 10.1038/sj.mt.6300351. Epub 2007 Nov 27. Mol Ther. 2008. PMID: 18223547 Free article. Review.
GJB2 mutations in Baluchi population.
Naghavi A, Nishimura C, Kahrizi K, Riazalhosseini Y, Bazazzadegan N, Mohseni M, Smith RJ, Najmabadi H. Naghavi A, et al. Among authors: smith rj. J Genet. 2008 Aug;87(2):195-7. doi: 10.1007/s12041-008-0031-5. J Genet. 2008. PMID: 18776652 No abstract available.
2,316 results