Johnson KR - Search Results

1

Hearing impairment in hypothyroid dwarf mice caused by mutations of the thyroid peroxidase gene.

Johnson KR, Gagnon LH, Longo-Guess CM, Harris BS, Chang B. Johnson KR, et al. J Assoc Res Otolaryngol. 2014 Feb;15(1):45-55. doi: 10.1007/s10162-013-0427-7. Epub 2013 Dec 3. J Assoc Res Otolaryngol. 2014. PMID: 24297261 Free PMC article.

2

The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear function.

Gagnon LH, Longo-Guess CM, Berryman M, Shin JB, Saylor KW, Yu H, Gillespie PG, Johnson KR. Gagnon LH, et al. Among authors: johnson kr. J Neurosci. 2006 Oct 4;26(40):10188-98. doi: 10.1523/JNEUROSCI.2166-06.2006. J Neurosci. 2006. PMID: 17021174 Free PMC article.

3

Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2.

Johnson KR, Marden CC, Ward-Bailey P, Gagnon LH, Bronson RT, Donahue LR. Johnson KR, et al. Mol Endocrinol. 2007 Jul;21(7):1593-602. doi: 10.1210/me.2007-0085. Epub 2007 Apr 17. Mol Endocrinol. 2007. PMID: 17440044

4

A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9.

Longo-Guess C, Gagnon LH, Bergstrom DE, Johnson KR. Longo-Guess C, et al. Among authors: johnson kr. Hear Res. 2007 Dec;234(1-2):21-8. doi: 10.1016/j.heares.2007.09.005. Epub 2007 Sep 29. Hear Res. 2007. PMID: 17967520 Free PMC article.

5

Separate and combined effects of Sod1 and Cdh23 mutations on age-related hearing loss and cochlear pathology in C57BL/6J mice.

Johnson KR, Yu H, Ding D, Jiang H, Gagnon LH, Salvi RJ. Johnson KR, et al. Hear Res. 2010 Sep 1;268(1-2):85-92. doi: 10.1016/j.heares.2010.05.002. Epub 2010 May 12. Hear Res. 2010. PMID: 20470874 Free PMC article.

6

Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice.

Johnson KR, Gagnon LH, Longo-Guess C, Kane KL. Johnson KR, et al. Neurobiol Aging. 2012 Aug;33(8):1720-9. doi: 10.1016/j.neurobiolaging.2011.05.009. Epub 2011 Jul 30. Neurobiol Aging. 2012. PMID: 21803452 Free PMC article.

7

Genetic background effects on age-related hearing loss associated with Cdh23 variants in mice.

Kane KL, Longo-Guess CM, Gagnon LH, Ding D, Salvi RJ, Johnson KR. Kane KL, et al. Among authors: johnson kr. Hear Res. 2012 Jan;283(1-2):80-8. doi: 10.1016/j.heares.2011.11.007. Epub 2011 Nov 22. Hear Res. 2012. PMID: 22138310 Free PMC article.

8

Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia.

Johnson KR, Longo-Guess CM, Gagnon LH. Johnson KR, et al. PLoS One. 2012;7(4):e36074. doi: 10.1371/journal.pone.0036074. Epub 2012 Apr 27. PLoS One. 2012. PMID: 22558334 Free PMC article.

9

A QTL on Chr 5 modifies hearing loss associated with the fascin-2 variant of DBA/2J mice.

Johnson KR, Longo-Guess CM, Gagnon LH. Johnson KR, et al. Mamm Genome. 2015 Aug;26(7-8):338-47. doi: 10.1007/s00335-015-9574-y. Epub 2015 Jun 20. Mamm Genome. 2015. PMID: 26092689 Free PMC article.

10

A hypomorphic mutation of the gamma-1 adaptin gene (Ap1g1) causes inner ear, retina, thyroid, and testes abnormalities in mice.

Johnson KR, Gagnon LH, Chang B. Johnson KR, et al. Mamm Genome. 2016 Jun;27(5-6):200-12. doi: 10.1007/s00335-016-9632-0. Epub 2016 Apr 18. Mamm Genome. 2016. PMID: 27090238 Free PMC article.

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