Longo-Guess CM - Search Results

1

Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation.

Longo-Guess CM, Gagnon LH, Fritzsch B, Johnson KR. Longo-Guess CM, et al. Mamm Genome. 2007 Sep;18(9):646-56. doi: 10.1007/s00335-007-9049-x. Epub 2007 Sep 18. Mamm Genome. 2007. PMID: 17876667 Free PMC article.

2

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. 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.

3

A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.

Longo-Guess CM, Gagnon LH, Cook SA, Wu J, Zheng QY, Johnson KR. Longo-Guess CM, et al. Proc Natl Acad Sci U S A. 2005 May 31;102(22):7894-9. doi: 10.1073/pnas.0500760102. Epub 2005 May 19. Proc Natl Acad Sci U S A. 2005. PMID: 15905332 Free PMC article.

4

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: longo guess cm. J Neurosci. 2006 Oct 4;26(40):10188-98. doi: 10.1523/JNEUROSCI.2166-06.2006. J Neurosci. 2006. PMID: 17021174 Free PMC article.

5

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. Among authors: longo guess cm. PLoS One. 2012;7(4):e36074. doi: 10.1371/journal.pone.0036074. Epub 2012 Apr 27. PLoS One. 2012. PMID: 22558334 Free PMC article.

6

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. Among authors: longo guess cm. 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.

7

A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice.

Johnson KR, Longo-Guess C, Gagnon LH, Yu H, Zheng QY. Johnson KR, et al. Genomics. 2008 Oct;92(4):219-25. doi: 10.1016/j.ygeno.2008.06.007. Epub 2008 Aug 15. Genomics. 2008. PMID: 18662770 Free PMC article.

8

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.

9

Hearing loss without overt metabolic acidosis in ATP6V1B1 deficient MRL mice, a new genetic model for non-syndromic deafness with enlarged vestibular aqueducts.

Tian C, Gagnon LH, Longo-Guess C, Korstanje R, Sheehan SM, Ohlemiller KK, Schrader AD, Lett JM, Johnson KR. Tian C, et al. Hum Mol Genet. 2017 Oct 1;26(19):3722-3735. doi: 10.1093/hmg/ddx257. Hum Mol Genet. 2017. PMID: 28934385 Free PMC article.

10

A spontaneous mouse deletion in Mctp1 uncovers a long-range cis-regulatory region crucial for NR2F1 function during inner ear development.

Tarchini B, Longo-Guess C, Tian C, Tadenev ALD, Devanney N, Johnson KR. Tarchini B, et al. Dev Biol. 2018 Nov 15;443(2):153-164. doi: 10.1016/j.ydbio.2018.09.011. Epub 2018 Sep 11. Dev Biol. 2018. PMID: 30217595 Free PMC article.

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