310 related articles for article (PubMed ID: 27693694)
1. Progressive hearing loss and degeneration of hair cell stereocilia in taperin gene knockout mice.
Chen M; Wang Q; Zhu GH; Hu P; Zhou Y; Wang T; Lai RS; Xiao ZA; Xie DH
Biochem Biophys Res Commun; 2016 Oct; 479(4):703-707. PubMed ID: 27693694
[TBL] [Abstract][Full Text] [Related]
2. Tprn is essential for the integrity of stereociliary rootlet in cochlear hair cells in mice.
Men Y; Li X; Tu H; Zhang A; Fu X; Wang Z; Jin Y; Hou C; Zhang T; Zhang S; Zhou Y; Li B; Li J; Sun X; Wang H; Gao J
Front Med; 2019 Dec; 13(6):690-704. PubMed ID: 30159668
[TBL] [Abstract][Full Text] [Related]
3. GRXCR2 Regulates Taperin Localization Critical for Stereocilia Morphology and Hearing.
Liu C; Luo N; Tung CY; Perrin BJ; Zhao B
Cell Rep; 2018 Oct; 25(5):1268-1280.e4. PubMed ID: 30380417
[TBL] [Abstract][Full Text] [Related]
4. Critical role of TPRN rings in the stereocilia for hearing.
Qi J; Tan F; Zhang L; Zhou Y; Zhang Z; Sun Q; Li N; Fang Y; Chen X; Wu Y; Zhong G; Chai R
Mol Ther; 2024 Jan; 32(1):204-217. PubMed ID: 37952086
[TBL] [Abstract][Full Text] [Related]
5. CLIC5 stabilizes membrane-actin filament linkages at the base of hair cell stereocilia in a molecular complex with radixin, taperin, and myosin VI.
Salles FT; Andrade LR; Tanda S; Grati M; Plona KL; Gagnon LH; Johnson KR; Kachar B; Berryman MA
Cytoskeleton (Hoboken); 2014 Jan; 71(1):61-78. PubMed ID: 24285636
[TBL] [Abstract][Full Text] [Related]
6. Methionine sulfoxide reductase B3 deficiency causes hearing loss due to stereocilia degeneration and apoptotic cell death in cochlear hair cells.
Kwon TJ; Cho HJ; Kim UK; Lee E; Oh SK; Bok J; Bae YC; Yi JK; Lee JW; Ryoo ZY; Lee SH; Lee KY; Kim HY
Hum Mol Genet; 2014 Mar; 23(6):1591-601. PubMed ID: 24191262
[TBL] [Abstract][Full Text] [Related]
7. The BEACH protein LRBA is required for hair bundle maintenance in cochlear hair cells and for hearing.
Vogl C; Butola T; Haag N; Hausrat TJ; Leitner MG; Moutschen M; Lefèbvre PP; Speckmann C; Garrett L; Becker L; Fuchs H; Hrabe de Angelis M; Nietzsche S; Kessels MM; Oliver D; Kneussel M; Kilimann MW; Strenzke N
EMBO Rep; 2017 Nov; 18(11):2015-2029. PubMed ID: 28893864
[TBL] [Abstract][Full Text] [Related]
8. Pejvakin, a Candidate Stereociliary Rootlet Protein, Regulates Hair Cell Function in a Cell-Autonomous Manner.
Kazmierczak M; Kazmierczak P; Peng AW; Harris SL; Shah P; Puel JL; Lenoir M; Franco SJ; Schwander M
J Neurosci; 2017 Mar; 37(13):3447-3464. PubMed ID: 28209736
[TBL] [Abstract][Full Text] [Related]
9. Reducing Taperin Expression Restores Hearing in Grxcr2 Mutant Mice.
Liu C; Luo N; Zhao B
Neuroscience; 2022 Aug; 498():85-92. PubMed ID: 35752427
[TBL] [Abstract][Full Text] [Related]
10. A humanized mouse model, demonstrating progressive hearing loss caused by MYO6 p.C442Y, is inherited in a semi-dominant pattern.
Wang J; Shen J; Guo L; Cheng C; Chai R; Shu Y; Li H
Hear Res; 2019 Aug; 379():79-88. PubMed ID: 31103816
[TBL] [Abstract][Full Text] [Related]
11. Tmc2 expression partially restores auditory function in a mouse model of DFNB7/B11 deafness caused by loss of Tmc1 function.
Nakanishi H; Kurima K; Pan B; Wangemann P; Fitzgerald TS; Géléoc GS; Holt JR; Griffith AJ
Sci Rep; 2018 Aug; 8(1):12125. PubMed ID: 30108230
[TBL] [Abstract][Full Text] [Related]
12. Elmod3 knockout leads to progressive hearing loss and abnormalities in cochlear hair cell stereocilia.
Li W; Feng Y; Chen A; Li T; Huang S; Liu J; Liu X; Liu Y; Gao J; Yan D; Sun J; Mei L; Liu X; Ling J
Hum Mol Genet; 2019 Dec; 28(24):4103-4112. PubMed ID: 31628468
[TBL] [Abstract][Full Text] [Related]
13. Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79.
Rehman AU; Morell RJ; Belyantseva IA; Khan SY; Boger ET; Shahzad M; Ahmed ZM; Riazuddin S; Khan SN; Riazuddin S; Friedman TB
Am J Hum Genet; 2010 Mar; 86(3):378-88. PubMed ID: 20170899
[TBL] [Abstract][Full Text] [Related]
14. Mutations of the mouse ELMO domain containing 1 gene (Elmod1) link small GTPase signaling to actin cytoskeleton dynamics in hair cell stereocilia.
Johnson KR; Longo-Guess CM; Gagnon LH
PLoS One; 2012; 7(4):e36074. PubMed ID: 22558334
[TBL] [Abstract][Full Text] [Related]
15. Stereocilia defects in waltzer (Cdh23), shaker1 (Myo7a) and double waltzer/shaker1 mutant mice.
Holme RH; Steel KP
Hear Res; 2002 Jul; 169(1-2):13-23. PubMed ID: 12121736
[TBL] [Abstract][Full Text] [Related]
16. A short splice form of Xin-actin binding repeat containing 2 (XIRP2) lacking the Xin repeats is required for maintenance of stereocilia morphology and hearing function.
Francis SP; Krey JF; Krystofiak ES; Cui R; Nanda S; Xu W; Kachar B; Barr-Gillespie PG; Shin JB
J Neurosci; 2015 Feb; 35(5):1999-2014. PubMed ID: 25653358
[TBL] [Abstract][Full Text] [Related]
17. OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67).
Thoenes M; Zimmermann U; Ebermann I; Ptok M; Lewis MA; Thiele H; Morlot S; Hess MM; Gal A; Eisenberger T; Bergmann C; Nürnberg G; Nürnberg P; Steel KP; Knipper M; Bolz HJ
Orphanet J Rare Dis; 2015 Feb; 10():15. PubMed ID: 25759012
[TBL] [Abstract][Full Text] [Related]
18. Disruption of the autism-related gene Pak1 causes stereocilia disorganization, hair cell loss, and deafness in mice.
Cheng C; Hou Y; Zhang Z; Wang Y; Lu L; Zhang L; Jiang P; Gao S; Fang Q; Zhu C; Gao J; Liu X; Xie W; Jia Z; Xu Z; Gao X; Chai R
J Genet Genomics; 2021 Apr; 48(4):324-332. PubMed ID: 34049799
[TBL] [Abstract][Full Text] [Related]
19. EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness.
Behlouli A; Bonnet C; Abdi S; Bouaita A; Lelli A; Hardelin JP; Schietroma C; Rous Y; Louha M; Cheknane A; Lebdi H; Boudjelida K; Makrelouf M; Zenati A; Petit C
Orphanet J Rare Dis; 2014 Apr; 9():55. PubMed ID: 24741995
[TBL] [Abstract][Full Text] [Related]
20. Diaphanous homolog 3 (Diap3) overexpression causes progressive hearing loss and inner hair cell defects in a transgenic mouse model of human deafness.
Schoen CJ; Burmeister M; Lesperance MM
PLoS One; 2013; 8(2):e56520. PubMed ID: 23441200
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
