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Items: 1 to 20 of 105

1.

Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation.

Xia A, Gao SS, Yuan T, Osborn A, Bress A, Pfister M, Maricich SM, Pereira FA, Oghalai JS.

Dis Model Mech. 2010 Mar-Apr;3(3-4):209-23. doi: 10.1242/dmm.004135. Epub 2010 Feb 8.

2.

Biophysical mechanisms underlying outer hair cell loss associated with a shortened tectorial membrane.

Liu CC, Gao SS, Yuan T, Steele C, Puria S, Oghalai JS.

J Assoc Res Otolaryngol. 2011 Oct;12(5):577-94. doi: 10.1007/s10162-011-0269-0. Epub 2011 May 13.

3.

Activity-dependent regulation of prestin expression in mouse outer hair cells.

Song Y, Xia A, Lee HY, Wang R, Ricci AJ, Oghalai JS.

J Neurophysiol. 2015 Jun 1;113(10):3531-42. doi: 10.1152/jn.00869.2014. Epub 2015 Mar 25.

4.

Structural and mechanical analysis of tectorial membrane Tecta mutants.

Gueta R, Levitt J, Xia A, Katz O, Oghalai JS, Rousso I.

Biophys J. 2011 May 18;100(10):2530-8. doi: 10.1016/j.bpj.2011.04.024.

5.

Prestin regulation and function in residual outer hair cells after noise-induced hearing loss.

Xia A, Song Y, Wang R, Gao SS, Clifton W, Raphael P, Chao SI, Pereira FA, Groves AK, Oghalai JS.

PLoS One. 2013 Dec 20;8(12):e82602. doi: 10.1371/journal.pone.0082602. eCollection 2013.

6.

Sharpened cochlear tuning in a mouse with a genetically modified tectorial membrane.

Russell IJ, Legan PK, Lukashkina VA, Lukashkin AN, Goodyear RJ, Richardson GP.

Nat Neurosci. 2007 Feb;10(2):215-23. Epub 2007 Jan 14.

7.

A deafness mutation isolates a second role for the tectorial membrane in hearing.

Legan PK, Lukashkina VA, Goodyear RJ, Lukashkin AN, Verhoeven K, Van Camp G, Russell IJ, Richardson GP.

Nat Neurosci. 2005 Aug;8(8):1035-42. Epub 2005 Jul 3.

PMID:
15995703
8.

Cochlear outer hair cells in a dominant-negative connexin26 mutant mouse preserve non-linear capacitance in spite of impaired distortion product otoacoustic emission.

Minekawa A, Abe T, Inoshita A, Iizuka T, Kakehata S, Narui Y, Koike T, Kamiya K, Okamura HO, Shinkawa H, Ikeda K.

Neuroscience. 2009 Dec 15;164(3):1312-9. doi: 10.1016/j.neuroscience.2009.08.043. Epub 2009 Aug 25.

PMID:
19712724
9.

A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

Legan PK, Lukashkina VA, Goodyear RJ, Kössi M, Russell IJ, Richardson GP.

Neuron. 2000 Oct;28(1):273-85.

10.

Three deaf mice: mouse models for TECTA-based human hereditary deafness reveal domain-specific structural phenotypes in the tectorial membrane.

Legan PK, Goodyear RJ, Morín M, Mencia A, Pollard H, Olavarrieta L, Korchagina J, Modamio-Hoybjor S, Mayo F, Moreno F, Moreno-Pelayo MA, Richardson GP.

Hum Mol Genet. 2014 May 15;23(10):2551-68. doi: 10.1093/hmg/ddt646. Epub 2013 Dec 20.

11.

Characterization of a spontaneous, recessive, missense mutation arising in the Tecta gene.

Moreno-Pelayo MA, Goodyear RJ, Mencía A, Modamio-Høybjør S, Legan PK, Olavarrieta L, Moreno F, Richardson GP.

J Assoc Res Otolaryngol. 2008 Jun;9(2):202-14. doi: 10.1007/s10162-008-0116-0. Epub 2008 May 2.

12.

Loss of mammal-specific tectorial membrane component carcinoembryonic antigen cell adhesion molecule 16 (CEACAM16) leads to hearing impairment at low and high frequencies.

Kammerer R, Rüttiger L, Riesenberg R, Schäuble C, Krupar R, Kamp A, Sunami K, Eisenried A, Hennenberg M, Grunert F, Bress A, Battaglia S, Schrewe H, Knipper M, Schneider MR, Zimmermann W.

J Biol Chem. 2012 Jun 22;287(26):21584-98. doi: 10.1074/jbc.M111.320481. Epub 2012 Apr 27.

13.

A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.

Pfister M, Thiele H, Van Camp G, Fransen E, Apaydin F, Aydin O, Leistenschneider P, Devoto M, Zenner HP, Blin N, Nürnberg P, Ozkarakas H, Kupka S.

Cell Physiol Biochem. 2004;14(4-6):369-76.

14.

TECTA mutations in Japanese with mid-frequency hearing loss affected by zona pellucida domain protein secretion.

Moteki H, Nishio SY, Hashimoto S, Takumi Y, Iwasaki S, Takeichi N, Fukuda S, Usami S.

J Hum Genet. 2012 Sep;57(9):587-92. doi: 10.1038/jhg.2012.73. Epub 2012 Jun 21.

PMID:
22718023
15.

Vibration of the organ of Corti within the cochlear apex in mice.

Gao SS, Wang R, Raphael PD, Moayedi Y, Groves AK, Zuo J, Applegate BE, Oghalai JS.

J Neurophysiol. 2014 Sep 1;112(5):1192-204. doi: 10.1152/jn.00306.2014. Epub 2014 Jun 11.

16.

Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

Verhoeven K, Van Laer L, Kirschhofer K, Legan PK, Hughes DC, Schatteman I, Verstreken M, Van Hauwe P, Coucke P, Chen A, Smith RJ, Somers T, Offeciers FE, Van de Heyning P, Richardson GP, Wachtler F, Kimberling WJ, Willems PJ, Govaerts PJ, Van Camp G.

Nat Genet. 1998 May;19(1):60-2. Erratum in: Nat Genet 1999 Apr;21(4):449.

PMID:
9590290
17.

Functional prestin transduction of immature outer hair cells from normal and prestin-null mice.

Xia A, Wooltorton JR, Palmer DJ, Ng P, Pereira FA, Eatock RA, Oghalai JS.

J Assoc Res Otolaryngol. 2008 Sep;9(3):307-20. doi: 10.1007/s10162-008-0121-3. Epub 2008 May 28.

18.

Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.

Alloisio N, Morlé L, Bozon M, Godet J, Verhoeven K, Van Camp G, Plauchu H, Muller P, Collet L, Lina-Granade G.

Eur J Hum Genet. 1999 Feb-Mar;7(2):255-8.

19.

Prestin-Dependence of Outer Hair Cell Survival and Partial Rescue of Outer Hair Cell Loss in PrestinV499G/Y501H Knockin Mice.

Cheatham MA, Edge RM, Homma K, Leserman EL, Dallos P, Zheng J.

PLoS One. 2015 Dec 18;10(12):e0145428. doi: 10.1371/journal.pone.0145428. eCollection 2015.

20.

A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.

Alasti F, Sanati MH, Behrouzifard AH, Sadeghi A, de Brouwer AP, Kremer H, Smith RJ, Van Camp G.

Int J Pediatr Otorhinolaryngol. 2008 Feb;72(2):249-55. Epub 2007 Nov 19.

PMID:
18022253
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