258 related articles for article (PubMed ID: 20095043)
1. Deafness and retinal degeneration in a novel USH1C knock-in mouse model.
Lentz JJ; Gordon WC; Farris HE; MacDonald GH; Cunningham DE; Robbins CA; Tempel BL; Bazan NG; Rubel EW; Oesterle EC; Keats BJ
Dev Neurobiol; 2010 Mar; 70(4):253-67. PubMed ID: 20095043
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Ush1c216A knock-in mouse survives Katrina.
Lentz J; Pan F; Ng SS; Deininger P; Keats B
Mutat Res; 2007 Mar; 616(1-2):139-44. PubMed ID: 17174357
[TBL] [Abstract][Full Text] [Related]
4. Ames Waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of Pcdh15 transcripts.
Haywood-Watson RJ; Ahmed ZM; Kjellstrom S; Bush RA; Takada Y; Hampton LL; Battey JF; Sieving PA; Friedman TB
Invest Ophthalmol Vis Sci; 2006 Jul; 47(7):3074-84. PubMed ID: 16799054
[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. Direct Delivery of Antisense Oligonucleotides to the Middle and Inner Ear Improves Hearing and Balance in Usher Mice.
Lentz JJ; Pan B; Ponnath A; Tran CM; Nist-Lund C; Galvin A; Goldberg H; Robillard KN; Jodelka FM; Farris HE; Huang J; Chen T; Zhu H; Zhou W; Rigo F; Hastings ML; Géléoc GSG
Mol Ther; 2020 Dec; 28(12):2662-2676. PubMed ID: 32818431
[TBL] [Abstract][Full Text] [Related]
7. Harmonin in the murine retina and the retinal phenotypes of Ush1c-mutant mice and human USH1C.
Williams DS; Aleman TS; Lillo C; Lopes VS; Hughes LC; Stone EM; Jacobson SG
Invest Ophthalmol Vis Sci; 2009 Aug; 50(8):3881-9. PubMed ID: 19324851
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness.
Lentz JJ; Jodelka FM; Hinrich AJ; McCaffrey KE; Farris HE; Spalitta MJ; Bazan NG; Duelli DM; Rigo F; Hastings ML
Nat Med; 2013 Mar; 19(3):345-50. PubMed ID: 23380860
[TBL] [Abstract][Full Text] [Related]
10. A mutation in Myo15 leads to Usher-like symptoms in LEW/Ztm-ci2 rats.
Held N; Smits BM; Gockeln R; Schubert S; Nave H; Northrup E; Cuppen E; Hedrich HJ; Wedekind D
PLoS One; 2011 Mar; 6(3):e15669. PubMed ID: 21479269
[TBL] [Abstract][Full Text] [Related]
11. Rescue of Outer Hair Cells with Antisense Oligonucleotides in Usher Mice Is Dependent on Age of Treatment.
Ponnath A; Depreux FF; Jodelka FM; Rigo F; Farris HE; Hastings ML; Lentz JJ
J Assoc Res Otolaryngol; 2018 Feb; 19(1):1-16. PubMed ID: 29027038
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.
Heckenlively JR; Chang B; Erway LC; Peng C; Hawes NL; Hageman GS; Roderick TH
Proc Natl Acad Sci U S A; 1995 Nov; 92(24):11100-4. PubMed ID: 7479945
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c.
Pan B; Askew C; Galvin A; Heman-Ackah S; Asai Y; Indzhykulian AA; Jodelka FM; Hastings ML; Lentz JJ; Vandenberghe LH; Holt JR; Géléoc GS
Nat Biotechnol; 2017 Mar; 35(3):264-272. PubMed ID: 28165476
[TBL] [Abstract][Full Text] [Related]
16. The USH1C 216G-->A splice-site mutation results in a 35-base-pair deletion.
Lentz J; Savas S; Ng SS; Athas G; Deininger P; Keats B
Hum Genet; 2005 Feb; 116(3):225-7. PubMed ID: 15578223
[TBL] [Abstract][Full Text] [Related]
17. A Natural Occurring Mouse Model with Adgrv1 Mutation of Usher Syndrome 2C and Characterization of its Recombinant Inbred Strains.
Yan W; Long P; Chen T; Liu W; Yao L; Ren Z; Li X; Wang J; Xue J; Tao Y; Zhang L; Zhang Z
Cell Physiol Biochem; 2018; 47(5):1883-1897. PubMed ID: 29961073
[TBL] [Abstract][Full Text] [Related]
18. Rescue of peripheral vestibular function in Usher syndrome mice using a splice-switching antisense oligonucleotide.
Vijayakumar S; Depreux FF; Jodelka FM; Lentz JJ; Rigo F; Jones TA; Hastings ML
Hum Mol Genet; 2017 Sep; 26(18):3482-3494. PubMed ID: 28633508
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
Johnson KR; Gagnon LH; Webb LS; Peters LL; Hawes NL; Chang B; Zheng QY
Hum Mol Genet; 2003 Dec; 12(23):3075-86. PubMed ID: 14519688
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]