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2. 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]
3. Usher proteins in inner ear structure and function. Ahmed ZM; Frolenkov GI; Riazuddin S Physiol Genomics; 2013 Nov; 45(21):987-9. PubMed ID: 24022220 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. The retinal phenotype of Usher syndrome: pathophysiological insights from animal models. El-Amraoui A; Petit C C R Biol; 2014 Mar; 337(3):167-77. PubMed ID: 24702843 [TBL] [Abstract][Full Text] [Related]
6. 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]
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9. 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]
10. 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]
11. Genetics and pathological mechanisms of Usher syndrome. Yan D; Liu XZ J Hum Genet; 2010 Jun; 55(6):327-35. PubMed ID: 20379205 [TBL] [Abstract][Full Text] [Related]
12. A homozygous MYO7A mutation associated to Usher syndrome and unilateral auditory neuropathy spectrum disorder. Xia H; Hu P; Yuan L; Xiong W; Xu H; Yi J; Yang Z; Deng X; Guo Y; Deng H Mol Med Rep; 2017 Oct; 16(4):4241-4246. PubMed ID: 28731162 [TBL] [Abstract][Full Text] [Related]
13. The Time Course of Deafness and Retinal Degeneration in a Kunming Mouse Model for Usher Syndrome. Yao L; Zhang L; Qi LS; Liu W; An J; Wang B; Xue JH; Zhang ZM PLoS One; 2016; 11(5):e0155619. PubMed ID: 27186975 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Microarray-based mutation analysis of 183 Spanish families with Usher syndrome. Jaijo T; Aller E; García-García G; Aparisi MJ; Bernal S; Avila-Fernández A; Barragán I; Baiget M; Ayuso C; Antiñolo G; Díaz-Llopis M; Külm M; Beneyto M; Nájera C; Millán JM Invest Ophthalmol Vis Sci; 2010 Mar; 51(3):1311-7. PubMed ID: 19683999 [TBL] [Abstract][Full Text] [Related]
16. Usher protein functions in hair cells and photoreceptors. Cosgrove D; Zallocchi M Int J Biochem Cell Biol; 2014 Jan; 46():80-9. PubMed ID: 24239741 [TBL] [Abstract][Full Text] [Related]
17. Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism. Jacobson SG; Cideciyan AV; Aleman TS; Sumaroka A; Roman AJ; Gardner LM; Prosser HM; Mishra M; Bech-Hansen NT; Herrera W; Schwartz SB; Liu XZ; Kimberling WJ; Steel KP; Williams DS Hum Mol Genet; 2008 Aug; 17(15):2405-15. PubMed ID: 18463160 [TBL] [Abstract][Full Text] [Related]
18. 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]
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20. Disease mechanisms and gene therapy for Usher syndrome. Géléoc GGS; El-Amraoui A Hear Res; 2020 Sep; 394():107932. PubMed ID: 32199721 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]