Longo-Guess C - Search Results

1

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.

2

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. Among authors: longo guess c. 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.

3

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: longo guess cm. 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.

4

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. Among authors: longo guess cm. 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.

5

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.

6

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.

7

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. Among authors: longo guess c. Hum Mol Genet. 2017 Oct 1;26(19):3722-3735. doi: 10.1093/hmg/ddx257. Hum Mol Genet. 2017. PMID: 28934385 Free PMC article.

8

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.

9

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.

10

The R109H variant of fascin-2, a developmentally regulated actin crosslinker in hair-cell stereocilia, underlies early-onset hearing loss of DBA/2J mice.

Shin JB, Longo-Guess CM, Gagnon LH, Saylor KW, Dumont RA, Spinelli KJ, Pagana JM, Wilmarth PA, David LL, Gillespie PG, Johnson KR. Shin JB, et al. J Neurosci. 2010 Jul 21;30(29):9683-94. doi: 10.1523/JNEUROSCI.1541-10.2010. J Neurosci. 2010. PMID: 20660251 Free PMC article.

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