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Items: 1 to 20 of 99

1.

Retrocochlear function of the peripheral deafness gene Cacna1d.

Satheesh SV, Kunert K, Rüttiger L, Zuccotti A, Schönig K, Friauf E, Knipper M, Bartsch D, Nothwang HG.

Hum Mol Genet. 2012 Sep 1;21(17):3896-909. doi: 10.1093/hmg/dds217. Epub 2012 Jun 7.

2.

Egr2::cre mediated conditional ablation of dicer disrupts histogenesis of mammalian central auditory nuclei.

Rosengauer E, Hartwich H, Hartmann AM, Rudnicki A, Satheesh SV, Avraham KB, Nothwang HG.

PLoS One. 2012;7(11):e49503. doi: 10.1371/journal.pone.0049503. Epub 2012 Nov 12.

3.

Null mutation of alpha1D Ca2+ channel gene results in deafness but no vestibular defect in mice.

Dou H, Vazquez AE, Namkung Y, Chu H, Cardell EL, Nie L, Parson S, Shin HS, Yamoah EN.

J Assoc Res Otolaryngol. 2004 Jun;5(2):215-26.

4.
5.

Downregulation of Cav1.3 calcium channel expression in the cochlea is associated with age-related hearing loss in C57BL/6J mice.

Chen J, Chu H, Xiong H, Yu Y, Huang X, Zhou L, Chen Q, Bing D, Liu Y, Wang S, Cui Y.

Neuroreport. 2013 Apr 17;24(6):313-7. doi: 10.1097/WNR.0b013e32835fa79c.

PMID:
23470431
6.
7.

Synaptic organization in cochlear inner hair cells deficient for the CaV1.3 (alpha1D) subunit of L-type Ca2+ channels.

Nemzou N RM, Bulankina AV, Khimich D, Giese A, Moser T.

Neuroscience. 2006 Sep 15;141(4):1849-60. Epub 2006 Jul 10.

PMID:
16828974
8.

[Mice lacking of voltage-gated L-type calcium channel alpha1D subunit have impaired sinoatrial node function and caused deafness].

Chu H, Zhou X, Song H, Cui Y, Xiong H, Zhou L.

Lin Chung Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2007 May;21(10):468-72. Chinese.

PMID:
17650821
9.

Lateral superior olive function in congenital deafness.

Couchman K, Garrett A, Deardorff AS, Rattay F, Resatz S, Fyffe R, Walmsley B, Leão RN.

Hear Res. 2011 Jul;277(1-2):163-75. doi: 10.1016/j.heares.2011.01.012. Epub 2011 Jan 27.

10.

Cav1.3 calcium channels are required for normal development of the auditory brainstem.

Hirtz JJ, Boesen M, Braun N, Deitmer JW, Kramer F, Lohr C, Müller B, Nothwang HG, Striessnig J, Löhrke S, Friauf E.

J Neurosci. 2011 Jun 1;31(22):8280-94. doi: 10.1523/JNEUROSCI.5098-10.2011.

11.

Developmental expression of Ca(v)1.3 (alpha1d) calcium channels in the mouse inner ear.

Hafidi A, Dulon D.

Brain Res Dev Brain Res. 2004 Jun 21;150(2):167-75. Erratum in: Brain Res Dev Brain Res. 2004 Oct 15;153(1):151.

PMID:
15158080
12.

Adenomatous Polyposis Coli Protein Deletion in Efferent Olivocochlear Neurons Perturbs Afferent Synaptic Maturation and Reduces the Dynamic Range of Hearing.

Hickman TT, Liberman MC, Jacob MH.

J Neurosci. 2015 Jun 17;35(24):9236-45. doi: 10.1523/JNEUROSCI.4384-14.2015.

13.

Two classes of outer hair cells along the tonotopic axis of the cochlea.

Engel J, Braig C, Rüttiger L, Kuhn S, Zimmermann U, Blin N, Sausbier M, Kalbacher H, Münkner S, Rohbock K, Ruth P, Winter H, Knipper M.

Neuroscience. 2006 Dec;143(3):837-49. Epub 2006 Oct 30.

PMID:
17074442
14.

Cochlear expression of a dominant-negative GJB2R75W construct delivered through the round window membrane in mice.

Maeda Y, Fukushima K, Kawasaki A, Nishizaki K, Smith RJ.

Neurosci Res. 2007 Jul;58(3):250-4. Epub 2007 Mar 24.

PMID:
17462767
15.

Expression and function of chloride transporters during development of inhibitory neurotransmission in the auditory brainstem.

Balakrishnan V, Becker M, Löhrke S, Nothwang HG, Güresir E, Friauf E.

J Neurosci. 2003 May 15;23(10):4134-45.

16.

L-type CaV1.2 deletion in the cochlea but not in the brainstem reduces noise vulnerability: implication for CaV1.2-mediated control of cochlear BDNF expression.

Zuccotti A, Lee SC, Campanelli D, Singer W, Satheesh SV, Patriarchi T, Geisler HS, Köpschall I, Rohbock K, Nothwang HG, Hu J, Hell JW, Schimmang T, Rüttiger L, Knipper M.

Front Mol Neurosci. 2013 Aug 9;6:20. doi: 10.3389/fnmol.2013.00020. eCollection 2013.

17.

Deafness in mice lacking the T-box transcription factor Tbx18 in otic fibrocytes.

Trowe MO, Maier H, Schweizer M, Kispert A.

Development. 2008 May;135(9):1725-34. doi: 10.1242/dev.014043. Epub 2008 Mar 19.

18.

Sensorineural hearing loss in insulin-like growth factor I-null mice: a new model of human deafness.

Cediel R, Riquelme R, Contreras J, Díaz A, Varela-Nieto I.

Eur J Neurosci. 2006 Jan;23(2):587-90.

PMID:
16420467
19.

LIMP-2/LGP85 deficiency causes ureteric pelvic junction obstruction, deafness and peripheral neuropathy in mice.

Gamp AC, Tanaka Y, Lüllmann-Rauch R, Wittke D, D'Hooge R, De Deyn PP, Moser T, Maier H, Hartmann D, Reiss K, Illert AL, von Figura K, Saftig P.

Hum Mol Genet. 2003 Mar 15;12(6):631-46.

20.

Suppression of the deafness and thyroid dysfunction in Thrb-null mice by an independent mutation in the Thra thyroid hormone receptor alpha gene.

Ng L, Rüsch A, Amma LL, Nordström K, Erway LC, Vennström B, Forrest D.

Hum Mol Genet. 2001 Nov 1;10(23):2701-8.

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