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Mapping quantitative trait loci for hearing loss in Black Swiss mice.

Drayton M, Noben-Trauth K.

Hear Res. 2006 Feb;212(1-2):128-39. Epub 2006 Jan 19.


High-frequency sensorineural hearing loss and its underlying genetics (Hfhl1 and Hfhl2) in NIH Swiss mice.

Keller JM, Neely HR, Latoche JR, Noben-Trauth K.

J Assoc Res Otolaryngol. 2011 Oct;12(5):617-31. doi: 10.1007/s10162-011-0270-7. Epub 2011 May 19.


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.

Mamm Genome. 2015 Aug;26(7-8):338-47. doi: 10.1007/s00335-015-9574-y. Epub 2015 Jun 20.


Polygenic inheritance of sensorineural hearing loss (Snhl2, -3, and -4) and organ of Corti patterning defect in the ALR/LtJ mouse strain.

Latoche JR, Neely HR, Noben-Trauth K.

Hear Res. 2011 May;275(1-2):150-9. doi: 10.1016/j.heares.2010.12.017. Epub 2010 Dec 24.


Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss.

Noben-Trauth K, Zheng QY, Johnson KR.

Nat Genet. 2003 Sep;35(1):21-3. Epub 2003 Aug 10.


Quantitative trait loci on chromosome 5 for susceptibility to frequency-specific effects on hearing in DBA/2J mice.

Suzuki S, Ishikawa M, Ueda T, Ohshiba Y, Miyasaka Y, Okumura K, Yokohama M, Taya C, Matsuoka K, Kikkawa Y.

Exp Anim. 2015;64(3):241-51. doi: 10.1538/expanim.14-0110. Epub 2015 Mar 10.


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.

Genomics. 2008 Oct;92(4):219-25. doi: 10.1016/j.ygeno.2008.06.007. Epub 2008 Aug 15.


Phenotype and genetics of progressive sensorineural hearing loss (Snhl1) in the LXS set of recombinant inbred strains of mice.

Noben-Trauth K, Latoche JR, Neely HR, Bennett B.

PLoS One. 2010 Jul 7;5(7):e11459. doi: 10.1371/journal.pone.0011459.


A novel QTL underlying early-onset, low-frequency hearing loss in BXD recombinant inbred strains.

Nagtegaal AP, Spijker S, Crins TT; Neuro-Bsik Mouse Phenomics Consortium, Borst JG.

Genes Brain Behav. 2012 Nov;11(8):911-20. doi: 10.1111/j.1601-183X.2012.00845.x. Epub 2012 Oct 8.


Natural variation in neuron number in mice is linked to a major quantitative trait locus on Chr 11.

Williams RW, Strom RC, Goldowitz D.

J Neurosci. 1998 Jan 1;18(1):138-46.


Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss.

Ikeda A, Zheng QY, Rosenstiel P, Maddatu T, Zuberi AR, Roopenian DC, North MA, Naggert JK, Johnson KR, Nishina PM.

Hum Mol Genet. 1999 Sep;8(9):1761-7.


Genomic structure, alternative splice forms and normal and mutant alleles of cadherin 23 (Cdh23).

Di Palma F, Pellegrino R, Noben-Trauth K.

Gene. 2001 Dec 27;281(1-2):31-41.


Mapping quantitative trait loci for serum insulin-like growth factor-1 levels in mice.

Rosen CJ, Churchill GA, Donahue LR, Shultz KL, Burgess JK, Powell DR, Ackert C, Beamer WG.

Bone. 2000 Oct;27(4):521-8. Erratum in: Bone 2000 Dec;27(6):877.


Strain background effects and genetic modifiers of hearing in mice.

Johnson KR, Zheng QY, Noben-Trauth K.

Brain Res. 2006 May 26;1091(1):79-88. Epub 2006 Mar 31. Review.


Mapping quantitative trait loci for seizure response to a GABAA receptor inverse agonist in mice.

Gershenfeld HK, Neumann PE, Li X, St Jean PL, Paul SM.

J Neurosci. 1999 May 15;19(10):3731-8.


Mapping of quantitative trait loci for hypnotic sensitivity to ethanol in crosses derived from the C57BL/6 and DBA/2 mouse strains.

Radcliffe RA, Bohl ML, Lowe MV, Cycowski CS, Wehner JM.

Alcohol Clin Exp Res. 2000 Sep;24(9):1335-42.


An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.

Manji SS, Miller KA, Williams LH, Andreasen L, Siboe M, Rose E, Bahlo M, Kuiper M, Dahl HH.

Am J Pathol. 2011 Aug;179(2):903-14. doi: 10.1016/j.ajpath.2011.04.002. Epub 2011 Jun 2.


Effects of Cdh23 single nucleotide substitutions on age-related hearing loss in C57BL/6 and 129S1/Sv mice and comparisons with congenic strains.

Johnson KR, Tian C, Gagnon LH, Jiang H, Ding D, Salvi R.

Sci Rep. 2017 Mar 13;7:44450. doi: 10.1038/srep44450.

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