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Items: 1 to 20 of 179

1.

Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.

Manji SS, Miller KA, Williams LH, Dahl HH.

Am J Pathol. 2012 Apr;180(4):1560-9. doi: 10.1016/j.ajpath.2011.12.034. Epub 2012 Feb 11.

PMID:
22330676
2.

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

Di Palma F, Holme RH, Bryda EC, Belyantseva IA, Pellegrino R, Kachar B, Steel KP, Noben-Trauth K.

Nat Genet. 2001 Jan;27(1):103-7.

PMID:
11138008
3.

A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family.

Zhao Y, Wang D, Zong L, Zhao F, Guan L, Zhang P, Shi W, Lan L, Wang H, Li Q, Han B, Yang L, Jin X, Wang J, Wang J, Wang Q.

PLoS One. 2014 May 14;9(5):e97064. doi: 10.1371/journal.pone.0097064. eCollection 2014.

4.

Mouse tales from Kresge: the deafness mouse.

Drury SS, Keats BJ.

J Am Acad Audiol. 2003 Aug;14(6):296-301. Review.

PMID:
14552423
5.

Progressive sensorineural hearing loss and normal vestibular function in a Dutch DFNB7/11 family with a novel mutation in TMC1.

de Heer AM, Collin RW, Huygen PL, Schraders M, Oostrik J, Rouwette M, Kunst HP, Kremer H, Cremers CW.

Audiol Neurootol. 2011;16(2):93-105. doi: 10.1159/000313282. Epub 2010 Jun 26.

PMID:
21252500
6.

[Advances in hereditary hearing loss caused by TMC1 mutations].

Wu K, Wang H, Wang Q.

Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Mar;51(3):224-9. doi: 10.3760/cma.j.issn.1673-0860.2016.03.016. Chinese.

PMID:
27033582
7.

Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.

Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC.

Hum Mol Genet. 2002 Aug 1;11(16):1887-98.

PMID:
12140191
8.

Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.

Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP.

Nat Genet. 2002 Mar;30(3):257-8. Epub 2002 Feb 19.

PMID:
11850623
9.

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.

Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF Jr, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ.

Nat Genet. 2002 Mar;30(3):277-84. Epub 2002 Feb 19.

PMID:
11850618
10.

The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon.

Rhodes CR, Parkinson N, Tsai H, Brooker D, Mansell S, Spurr N, Hunter AJ, Steel KP, Brown SD.

J Neurocytol. 2003 Nov;32(9):1143-54.

PMID:
15044845
11.

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.

12.

Mutations of TMC1 cause deafness by disrupting mechanoelectrical transduction.

Nakanishi H, Kurima K, Kawashima Y, Griffith AJ.

Auris Nasus Larynx. 2014 Oct;41(5):399-408. doi: 10.1016/j.anl.2014.04.001. Epub 2014 Jun 2.

13.

Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family.

Gao X, Su Y, Guan LP, Yuan YY, Huang SS, Lu Y, Wang GJ, Han MY, Yu F, Song YS, Zhu QY, Wu J, Dai P.

PLoS One. 2013 May 14;8(5):e63026. doi: 10.1371/journal.pone.0063026. Print 2013.

14.

Tailchaser (Tlc): a new mouse mutation affecting hair bundle differentiation and hair cell survival.

Kiernan AE, Zalzman M, Fuchs H, Hrabe de Angelis M, Balling R, Steel KP, Avraham KB.

J Neurocytol. 1999 Oct-Nov;28(10-11):969-85.

PMID:
10900098
15.

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1.

Young TL, Ives E, Lynch E, Person R, Snook S, MacLaren L, Cater T, Griffin A, Fernandez B, Lee MK, King MC.

Hum Mol Genet. 2001 Oct 15;10(22):2509-14. Erratum in: Hum Mol Genet 2001 Dec 15;10(26):3111. Cator T [corrected to Cater T].

PMID:
11709538
16.

Localization of efferent neurotransmitters in the inner ear of the homozygous Bronx waltzer mutant mouse.

Kong WJ, Scholtz AW, Hussl B, Kammen-Jolly K, Schrott-Fischer A.

Hear Res. 2002 May;167(1-2):136-55.

PMID:
12117537
17.

Ultrastructural and physiological defects in the cochlea of the Mpv17 mouse strain. A comparison between young and old adult animals.

Meyer zum Gottesberge AM, Felix H, Reuter A, Weiher H.

Hear Res. 2001 Jun;156(1-2):69-80.

PMID:
11377883
18.

Mutations in Mcoln3 associated with deafness and pigmentation defects in varitint-waddler (Va) mice.

Di Palma F, Belyantseva IA, Kim HJ, Vogt TF, Kachar B, Noben-Trauth K.

Proc Natl Acad Sci U S A. 2002 Nov 12;99(23):14994-9. Epub 2002 Oct 25.

19.

A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice.

Sato H, Suzuki T, Ikeda K, Masuya H, Sezutsu H, Kaneda H, Kobayashi K, Miura I, Kurihara Y, Yokokura S, Nishida K, Tamai M, Gondo Y, Noda T, Wakana S.

Mol Vis. 2010 Mar 10;16:378-91.

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