1037 related articles for article (PubMed ID: 16545802)
1. 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]
2. 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]
3. Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C).
Reiners J; Märker T; Jürgens K; Reidel B; Wolfrum U
Mol Vis; 2005 May; 11():347-55. PubMed ID: 15928608
[TBL] [Abstract][Full Text] [Related]
4. The usher syndromes.
Keats BJ; Corey DP
Am J Med Genet; 1999 Sep; 89(3):158-66. PubMed ID: 10704190
[TBL] [Abstract][Full Text] [Related]
5. A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells.
Maerker T; van Wijk E; Overlack N; Kersten FF; McGee J; Goldmann T; Sehn E; Roepman R; Walsh EJ; Kremer H; Wolfrum U
Hum Mol Genet; 2008 Jan; 17(1):71-86. PubMed ID: 17906286
[TBL] [Abstract][Full Text] [Related]
6. Characterization of the ternary Usher syndrome SANS/ush2a/whirlin protein complex.
Sorusch N; Bauß K; Plutniok J; Samanta A; Knapp B; Nagel-Wolfrum K; Wolfrum U
Hum Mol Genet; 2017 Mar; 26(6):1157-1172. PubMed ID: 28137943
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Usher syndrome: from genetics to pathogenesis.
Petit C
Annu Rev Genomics Hum Genet; 2001; 2():271-97. PubMed ID: 11701652
[TBL] [Abstract][Full Text] [Related]
9. An update on the genetics of usher syndrome.
Millán JM; Aller E; Jaijo T; Blanco-Kelly F; Gimenez-Pardo A; Ayuso C
J Ophthalmol; 2011; 2011():417217. PubMed ID: 21234346
[TBL] [Abstract][Full Text] [Related]
10. SANS (USH1G) expression in developing and mature mammalian retina.
Overlack N; Maerker T; Latz M; Nagel-Wolfrum K; Wolfrum U
Vision Res; 2008 Feb; 48(3):400-12. PubMed ID: 17923142
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. The roles of USH1 proteins and PDZ domain-containing USH proteins in USH2 complex integrity in cochlear hair cells.
Zou J; Chen Q; Almishaal A; Mathur PD; Zheng T; Tian C; Zheng QY; Yang J
Hum Mol Genet; 2017 Feb; 26(3):624-636. PubMed ID: 28031293
[TBL] [Abstract][Full Text] [Related]
13. A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing loss.
Ebermann I; Scholl HP; Charbel Issa P; Becirovic E; Lamprecht J; Jurklies B; Millán JM; Aller E; Mitter D; Bolz H
Hum Genet; 2007 Apr; 121(2):203-11. PubMed ID: 17171570
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Bolz H; von Brederlow B; Ramírez A; Bryda EC; Kutsche K; Nothwang HG; Seeliger M; del C-Salcedó Cabrera M; Vila MC; Molina OP; Gal A; Kubisch C
Nat Genet; 2001 Jan; 27(1):108-12. PubMed ID: 11138009
[TBL] [Abstract][Full Text] [Related]
17. [Syndromic hereditary deafness. Usher's syndrome. Oto-neurologic and genetic factors].
Espinós C; Pérez-Garrigues H; Beneyto M; Vilela C; Rodrigo O; Nájera C
An Otorrinolaringol Ibero Am; 1999; 26(1):83-95. PubMed ID: 10091368
[TBL] [Abstract][Full Text] [Related]
18. Extended mutation spectrum of Usher syndrome in Finland.
Västinsalo H; Jalkanen R; Bergmann C; Neuhaus C; Kleemola L; Jauhola L; Bolz HJ; Sankila EM
Acta Ophthalmol; 2013 Jun; 91(4):325-34. PubMed ID: 22681893
[TBL] [Abstract][Full Text] [Related]
19. Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Weil D; Blanchard S; Kaplan J; Guilford P; Gibson F; Walsh J; Mburu P; Varela A; Levilliers J; Weston MD
Nature; 1995 Mar; 374(6517):60-1. PubMed ID: 7870171
[TBL] [Abstract][Full Text] [Related]
20. Mutations in myosin VIIA (MYO7A) and usherin (USH2A) in Spanish patients with Usher syndrome types I and II, respectively.
Nájera C; Beneyto M; Blanca J; Aller E; Fontcuberta A; Millán JM; Ayuso C
Hum Mutat; 2002 Jul; 20(1):76-7. PubMed ID: 12112664
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
