707 related articles for article (PubMed ID: 16301217)
1. 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]
2. Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells.
El-Amraoui A; Petit C
J Cell Sci; 2005 Oct; 118(Pt 20):4593-603. PubMed ID: 16219682
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2.
Reiners J; van Wijk E; Märker T; Zimmermann U; Jürgens K; te Brinke H; Overlack N; Roepman R; Knipper M; Kremer H; Wolfrum U
Hum Mol Genet; 2005 Dec; 14(24):3933-43. PubMed ID: 16301216
[TBL] [Abstract][Full Text] [Related]
5. A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Verpy E; Leibovici M; Zwaenepoel I; Liu XZ; Gal A; Salem N; Mansour A; Blanchard S; Kobayashi I; Keats BJ; Slim R; Petit C
Nat Genet; 2000 Sep; 26(1):51-5. PubMed ID: 10973247
[TBL] [Abstract][Full Text] [Related]
6. [Usher syndrome type I and the differentiation of inner ear sensory cells' hair bundles].
El-Amraoui A; Lefèvre G; Hardelin JP; Petit C
Med Sci (Paris); 2005; 21(8-9):737-40. PubMed ID: 16115459
[TBL] [Abstract][Full Text] [Related]
7. Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly.
Delprat B; Michel V; Goodyear R; Yamasaki Y; Michalski N; El-Amraoui A; Perfettini I; Legrain P; Richardson G; Hardelin JP; Petit C
Hum Mol Genet; 2005 Feb; 14(3):401-10. PubMed ID: 15590698
[TBL] [Abstract][Full Text] [Related]
8. Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II.
Dreyer B; Brox V; Tranebjaerg L; Rosenberg T; Sadeghi AM; Möller C; Nilssen O
Hum Mutat; 2008 Mar; 29(3):451. PubMed ID: 18273898
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment.
Schneider E; Märker T; Daser A; Frey-Mahn G; Beyer V; Farcas R; Schneider-Rätzke B; Kohlschmidt N; Grossmann B; Bauss K; Napiontek U; Keilmann A; Bartsch O; Zechner U; Wolfrum U; Haaf T
Hum Mol Genet; 2009 Feb; 18(4):655-66. PubMed ID: 19028668
[TBL] [Abstract][Full Text] [Related]
11. Correlation of expression of the actin filament-bundling protein espin with stereociliary bundle formation in the developing inner ear.
Li H; Liu H; Balt S; Mann S; Corrales CE; Heller S
J Comp Neurol; 2004 Jan; 468(1):125-34. PubMed ID: 14648695
[TBL] [Abstract][Full Text] [Related]
12. Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.
Lagziel A; Ahmed ZM; Schultz JM; Morell RJ; Belyantseva IA; Friedman TB
Dev Biol; 2005 Apr; 280(2):295-306. PubMed ID: 15882574
[TBL] [Abstract][Full Text] [Related]
13. Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning.
Michalski N; Michel V; Bahloul A; Lefèvre G; Barral J; Yagi H; Chardenoux S; Weil D; Martin P; Hardelin JP; Sato M; Petit C
J Neurosci; 2007 Jun; 27(24):6478-88. PubMed ID: 17567809
[TBL] [Abstract][Full Text] [Related]
14. A domain-specific usherin/collagen IV interaction may be required for stable integration into the basement membrane superstructure.
Bhattacharya G; Kalluri R; Orten DJ; Kimberling WJ; Cosgrove D
J Cell Sci; 2004 Jan; 117(Pt 2):233-42. PubMed ID: 14676276
[TBL] [Abstract][Full Text] [Related]
15. Mutant analysis reveals whirlin as a dynamic organizer in the growing hair cell stereocilium.
Kikkawa Y; Mburu P; Morse S; Kominami R; Townsend S; Brown SD
Hum Mol Genet; 2005 Feb; 14(3):391-400. PubMed ID: 15590699
[TBL] [Abstract][Full Text] [Related]
16. Evidence for functional importance of usherin/fibronectin interactions in retinal basement membranes.
Bhattacharya G; Cosgrove D
Biochemistry; 2005 Aug; 44(34):11518-24. PubMed ID: 16114888
[TBL] [Abstract][Full Text] [Related]
17. Interactions in the network of Usher syndrome type 1 proteins.
Adato A; Michel V; Kikkawa Y; Reiners J; Alagramam KN; Weil D; Yonekawa H; Wolfrum U; El-Amraoui A; Petit C
Hum Mol Genet; 2005 Feb; 14(3):347-56. PubMed ID: 15590703
[TBL] [Abstract][Full Text] [Related]
18. Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells.
Liu X; Bulgakov OV; Darrow KN; Pawlyk B; Adamian M; Liberman MC; Li T
Proc Natl Acad Sci U S A; 2007 Mar; 104(11):4413-8. PubMed ID: 17360538
[TBL] [Abstract][Full Text] [Related]
19. Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin alpha8beta1.
Littlewood Evans A; Müller U
Nat Genet; 2000 Apr; 24(4):424-8. PubMed ID: 10742111
[TBL] [Abstract][Full Text] [Related]
20. Lack of PDZD7 long isoform disrupts ankle-link complex and causes hearing loss in mice.
Du H; Zou L; Ren R; Li N; Li J; Wang Y; Sun J; Yang J; Xiong W; Xu Z
FASEB J; 2020 Jan; 34(1):1136-1149. PubMed ID: 31914662
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
