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Journal Abstract Search
700 related items for 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 15; 14(24):3921-32. PubMed ID: 16301217 [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 15; 118(Pt 20):4593-603. PubMed ID: 16219682 [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 15; 83(1):97-119. PubMed ID: 16545802 [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 15; 29(3):451. PubMed ID: 18273898 [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 15; 135(8):1427-37. PubMed ID: 18339676 [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 15; 18(4):655-66. PubMed ID: 19028668 [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 01; 468(1):125-34. PubMed ID: 14648695 [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 15; 280(2):295-306. PubMed ID: 15882574 [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 13; 27(24):6478-88. PubMed ID: 17567809 [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 01; 14(3):391-400. PubMed ID: 15590699 [Abstract] [Full Text] [Related]
16. Evidence for functional importance of usherin/fibronectin interactions in retinal basement membranes. Bhattacharya G, Cosgrove D. Biochemistry; 2005 Aug 30; 44(34):11518-24. PubMed ID: 16114888 [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 01; 14(3):347-56. PubMed ID: 15590703 [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 13; 104(11):4413-8. PubMed ID: 17360538 [Abstract] [Full Text] [Related]