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Results: 1 to 20 of 50

1.

Genome-wide linkage analyses identify Hfhl1 and Hfhl3 with frequency-specific effects on the hearing spectrum of NIH Swiss mice.

Keller JM, Noben-Trauth K.

BMC Genet. 2012 Apr 27;13:32. doi: 10.1186/1471-2156-13-32.

PMID:
22540152
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

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.

PMID:
21594677
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human.

Charizopoulou N, Lelli A, Schraders M, Ray K, Hildebrand MS, Ramesh A, Srisailapathy CR, Oostrik J, Admiraal RJ, Neely HR, Latoche JR, Smith RJ, Northup JK, Kremer H, Holt JR, Noben-Trauth K.

Nat Commun. 2011 Feb 15;2:201. doi: 10.1038/ncomms1200.

PMID:
21326233
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

The TRPML3 channel: from gene to function.

Noben-Trauth K.

Adv Exp Med Biol. 2011;704:229-37. doi: 10.1007/978-94-007-0265-3_13. Review.

PMID:
21290299
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
21185929
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Ectopic mineralization in the middle ear and chronic otitis media with effusion caused by RPL38 deficiency in the Tail-short (Ts) mouse.

Noben-Trauth K, Latoche JR.

J Biol Chem. 2011 Jan 28;286(4):3079-93. doi: 10.1074/jbc.M110.184598. Epub 2010 Nov 9.

PMID:
21062742
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

SOBP is mutated in syndromic and nonsyndromic intellectual disability and is highly expressed in the brain limbic system.

Birk E, Har-Zahav A, Manzini CM, Pasmanik-Chor M, Kornreich L, Walsh CA, Noben-Trauth K, Albin A, Simon AJ, Colleaux L, Morad Y, Rainshtein L, Tischfield DJ, Wang P, Magal N, Maya I, Shoshani N, Rechavi G, Gothelf D, Maydan G, Shohat M, Basel-Vanagaite L.

Am J Hum Genet. 2010 Nov 12;87(5):694-700. doi: 10.1016/j.ajhg.2010.10.005. Epub 2010 Oct 28.

PMID:
21035105
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

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.

PMID:
20628639
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Inheritance patterns of progressive hearing loss in laboratory strains of mice.

Noben-Trauth K, Johnson KR.

Brain Res. 2009 Jun 24;1277:42-51. doi: 10.1016/j.brainres.2009.02.012. Epub 2009 Feb 21. Review.

PMID:
19236853
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

TRPML3 mutations cause impaired mechano-electrical transduction and depolarization by an inward-rectifier cation current in auditory hair cells of varitint-waddler mice.

van Aken AF, Atiba-Davies M, Marcotti W, Goodyear RJ, Bryant JE, Richardson GP, Noben-Trauth K, Kros CJ.

J Physiol. 2008 Nov 15;586(Pt 22):5403-18. doi: 10.1113/jphysiol.2008.156992. Epub 2008 Sep 18.

PMID:
18801844
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Jxc1/Sobp, encoding a nuclear zinc finger protein, is critical for cochlear growth, cell fate, and patterning of the organ of corti.

Chen Z, Montcouquiol M, Calderon R, Jenkins NA, Copeland NG, Kelley MW, Noben-Trauth K.

J Neurosci. 2008 Jun 25;28(26):6633-41. doi: 10.1523/JNEUROSCI.1280-08.2008.

PMID:
18579736
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Single nucleotide polymorphisms in the cadherin 23 (CDH23) gene in Polish workers exposed to industrial noise.

Sliwinska-Kowalska M, Noben-Trauth K, Pawelczyk M, Kowalski TJ.

Am J Hum Biol. 2008 Jul-Aug;20(4):481-3. doi: 10.1002/ajhb.20744.

PMID:
18348277
[PubMed - indexed for MEDLINE]
13.

Normal hearing in alpha-galactosidase A-deficient mice, the mouse model for Fabry disease.

Noben-Trauth K, Neely H, Brady RO.

Hear Res. 2007 Dec;234(1-2):10-4. Epub 2007 Sep 14.

PMID:
17933476
[PubMed - indexed for MEDLINE]
14.

TRPML3 and hearing loss in the varitint-waddler mouse.

Atiba-Davies M, Noben-Trauth K.

Biochim Biophys Acta. 2007 Aug;1772(8):1028-31. Epub 2007 Jan 23. Review.

PMID:
17329082
[PubMed - indexed for MEDLINE]
Free Article
15.

Cochlear developmental defect and background-dependent hearing thresholds in the Jackson circler (jc) mutant mouse.

Calderon A, Derr A, Stagner BB, Johnson KR, Martin G, Noben-Trauth K.

Hear Res. 2006 Nov;221(1-2):44-58. Epub 2006 Sep 7.

PMID:
16962269
[PubMed - indexed for MEDLINE]
16.

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.

PMID:
16579977
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

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.

PMID:
16426780
[PubMed - indexed for MEDLINE]
18.

Balanced levels of Espin are critical for stereociliary growth and length maintenance.

Rzadzinska A, Schneider M, Noben-Trauth K, Bartles JR, Kachar B.

Cell Motil Cytoskeleton. 2005 Nov;62(3):157-65.

PMID:
16206170
[PubMed - indexed for MEDLINE]
19.

Sustained cadherin 23 expression in young and adult cochlea of normal and hearing-impaired mice.

Rzadzinska AK, Derr A, Kachar B, Noben-Trauth K.

Hear Res. 2005 Oct;208(1-2):114-21. Epub 2005 Jul 6.

PMID:
16005171
[PubMed - indexed for MEDLINE]
20.

Cellular and molecular function of mucolipins (TRPML) and polycystin 2 (TRPP2).

Qian F, Noben-Trauth K.

Pflugers Arch. 2005 Oct;451(1):277-85. Epub 2005 Jun 22. Review.

PMID:
15971078
[PubMed - indexed for MEDLINE]

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