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Year | Number of Results |
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2000 | 1 |
2001 | 2 |
2004 | 1 |
2009 | 1 |
2024 | 0 |
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5 results
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Page 1
Selective activation of nuclear factor kappa B in the cochlea by sensory and inflammatory stress.
Neuroscience. 2009 May 5;160(2):530-9. doi: 10.1016/j.neuroscience.2009.02.073. Epub 2009 Mar 11.
Neuroscience. 2009.
PMID: 19285117
Free PMC article.
Isolation from cochlea of a novel human intronless gene with predominant fetal expression.
Resendes BL, Kuo SF, Robertson NG, Giersch AB, Honrubia D, Ohara O, Adams JC, Morton CC.
Resendes BL, et al.
J Assoc Res Otolaryngol. 2004 Jun;5(2):185-202. doi: 10.1007/s10162-003-4042-x.
J Assoc Res Otolaryngol. 2004.
PMID: 15357420
Free PMC article.
Item in Clipboard
Potassium ion recycling pathway via gap junction systems in the mammalian cochlea and its interruption in hereditary nonsyndromic deafness.
Kikuchi T, Adams JC, Miyabe Y, So E, Kobayashi T.
Kikuchi T, et al.
Med Electron Microsc. 2000;33(2):51-6. doi: 10.1007/s007950070001.
Med Electron Microsc. 2000.
PMID: 11810458
Review.
Item in Clipboard
Mice overexpressing genes from the 22q11 region deleted in velo-cardio-facial syndrome/DiGeorge syndrome have middle and inner ear defects.
Funke B, Epstein JA, Kochilas LK, Lu MM, Pandita RK, Liao J, Bauerndistel R, Schüler T, Schorle H, Brown MC, Adams J, Morrow BE.
Funke B, et al.
Hum Mol Genet. 2001 Oct 15;10(22):2549-56. doi: 10.1093/hmg/10.22.2549.
Hum Mol Genet. 2001.
PMID: 11709542
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Inner ear localization of mRNA and protein products of COCH, mutated in the sensorineural deafness and vestibular disorder, DFNA9.
Robertson NG, Resendes BL, Lin JS, Lee C, Aster JC, Adams JC, Morton CC.
Robertson NG, et al.
Hum Mol Genet. 2001 Oct 15;10(22):2493-500. doi: 10.1093/hmg/10.22.2493.
Hum Mol Genet. 2001.
PMID: 11709536
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