These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
407 related articles for article (PubMed ID: 21073336)
1. How the genetics of deafness illuminates auditory physiology. Richardson GP; de Monvel JB; Petit C Annu Rev Physiol; 2011; 73():311-34. PubMed ID: 21073336 [TBL] [Abstract][Full Text] [Related]
2. [Molecular mechanisms underlying function of hair bundle: study on genetic deafness in mouse models]. Liang LZ; Zheng BJ; Zheng J; Fang F; Wu Y; Guan MX Sheng Li Xue Bao; 2012 Aug; 64(4):481-8. PubMed ID: 22907311 [TBL] [Abstract][Full Text] [Related]
3. Hair-Bundle Links: Genetics as the Gateway to Function. Richardson GP; Petit C Cold Spring Harb Perspect Med; 2019 Dec; 9(12):. PubMed ID: 30617060 [TBL] [Abstract][Full Text] [Related]
4. Linking genes underlying deafness to hair-bundle development and function. Petit C; Richardson GP Nat Neurosci; 2009 Jun; 12(6):703-10. PubMed ID: 19471269 [TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 15995703 [TBL] [Abstract][Full Text] [Related]
6. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Adato A; Lefèvre G; Delprat B; Michel V; Michalski N; Chardenoux S; Weil D; El-Amraoui A; Petit C Hum Mol Genet; 2005 Dec; 14(24):3921-32. PubMed ID: 16301217 [TBL] [Abstract][Full Text] [Related]
7. A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Lefèvre G; Michel V; Weil D; Lepelletier L; Bizard E; Wolfrum U; Hardelin JP; Petit C Development; 2008 Apr; 135(8):1427-37. PubMed ID: 18339676 [TBL] [Abstract][Full Text] [Related]
8. Auditory and vestibular hair cell stereocilia: relationship between functionality and inner ear disease. Ciuman RR J Laryngol Otol; 2011 Oct; 125(10):991-1003. PubMed ID: 21774850 [TBL] [Abstract][Full Text] [Related]
9. More deafness genes. Steel KP; Brown SD Science; 1998 May; 280(5368):1403. PubMed ID: 9634418 [No Abstract] [Full Text] [Related]
10. Molecular basis of human Usher syndrome: deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease. Reiners J; Nagel-Wolfrum K; Jürgens K; Märker T; Wolfrum U Exp Eye Res; 2006 Jul; 83(1):97-119. PubMed ID: 16545802 [TBL] [Abstract][Full Text] [Related]
12. Usher syndrome and non-syndromic deafness: Functions of different whirlin isoforms in the cochlea, vestibular organs, and retina. Mathur PD; Yang J Hear Res; 2019 Apr; 375():14-24. PubMed ID: 30831381 [TBL] [Abstract][Full Text] [Related]
13. Hair cells, plasma membrane Ca²⁺ ATPase and deafness. Giacomello M; De Mario A; Primerano S; Brini M; Carafoli E Int J Biochem Cell Biol; 2012 May; 44(5):679-83. PubMed ID: 22349217 [TBL] [Abstract][Full Text] [Related]
14. Development of the hair bundle and mechanotransduction. Nayak GD; Ratnayaka HS; Goodyear RJ; Richardson GP Int J Dev Biol; 2007; 51(6-7):597-608. PubMed ID: 17891720 [TBL] [Abstract][Full Text] [Related]
15. Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane. Verpy E; Leibovici M; Michalski N; Goodyear RJ; Houdon C; Weil D; Richardson GP; Petit C J Comp Neurol; 2011 Feb; 519(2):194-210. PubMed ID: 21165971 [TBL] [Abstract][Full Text] [Related]
16. A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells. Schwander M; Xiong W; Tokita J; Lelli A; Elledge HM; Kazmierczak P; Sczaniecka A; Kolatkar A; Wiltshire T; Kuhn P; Holt JR; Kachar B; Tarantino L; Müller U Proc Natl Acad Sci U S A; 2009 Mar; 106(13):5252-7. PubMed ID: 19270079 [TBL] [Abstract][Full Text] [Related]
17. The mechanosensory structure of the hair cell requires clarin-1, a protein encoded by Usher syndrome III causative gene. Geng R; Melki S; Chen DH; Tian G; Furness DN; Oshima-Takago T; Neef J; Moser T; Askew C; Horwitz G; Holt JR; Imanishi Y; Alagramam KN J Neurosci; 2012 Jul; 32(28):9485-98. PubMed ID: 22787034 [TBL] [Abstract][Full Text] [Related]
18. CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells. Giese APJ; Tang YQ; Sinha GP; Bowl MR; Goldring AC; Parker A; Freeman MJ; Brown SDM; Riazuddin S; Fettiplace R; Schafer WR; Frolenkov GI; Ahmed ZM Nat Commun; 2017 Jun; 8(1):43. PubMed ID: 28663585 [TBL] [Abstract][Full Text] [Related]
20. Control of a hair bundle's mechanosensory function by its mechanical load. Salvi JD; Ó Maoiléidigh D; Fabella BA; Tobin M; Hudspeth AJ Proc Natl Acad Sci U S A; 2015 Mar; 112(9):E1000-9. PubMed ID: 25691749 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]