BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

267 related articles for article (PubMed ID: 24334608)

  • 1. Deletion of PDZD7 disrupts the Usher syndrome type 2 protein complex in cochlear hair cells and causes hearing loss in mice.
    Zou J; Zheng T; Ren C; Askew C; Liu XP; Pan B; Holt JR; Wang Y; Yang J
    Hum Mol Genet; 2014 May; 23(9):2374-90. PubMed ID: 24334608
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Whirlin and PDZ domain-containing 7 (PDZD7) proteins are both required to form the quaternary protein complex associated with Usher syndrome type 2.
    Chen Q; Zou J; Shen Z; Zhang W; Yang J
    J Biol Chem; 2014 Dec; 289(52):36070-88. PubMed ID: 25406310
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Localization of PDZD7 to the stereocilia ankle-link associates this scaffolding protein with the Usher syndrome protein network.
    Grati M; Shin JB; Weston MD; Green J; Bhat MA; Gillespie PG; Kachar B
    J Neurosci; 2012 Oct; 32(41):14288-93. PubMed ID: 23055499
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Individual USH2 proteins make distinct contributions to the ankle link complex during development of the mouse cochlear stereociliary bundle.
    Zou J; Mathur PD; Zheng T; Wang Y; Almishaal A; Park AH; Yang J
    Hum Mol Genet; 2015 Dec; 24(24):6944-57. PubMed ID: 26401052
    [TBL] [Abstract][Full Text] [Related]  

  • 9. PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.
    Ebermann I; Phillips JB; Liebau MC; Koenekoop RK; Schermer B; Lopez I; Schäfer E; Roux AF; Dafinger C; Bernd A; Zrenner E; Claustres M; Blanco B; Nürnberg G; Nürnberg P; Ruland R; Westerfield M; Benzing T; Bolz HJ
    J Clin Invest; 2010 Jun; 120(6):1812-23. PubMed ID: 20440071
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 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. Whirlin replacement restores the formation of the USH2 protein complex in whirlin knockout photoreceptors.
    Zou J; Luo L; Shen Z; Chiodo VA; Ambati BK; Hauswirth WW; Yang J
    Invest Ophthalmol Vis Sci; 2011 Apr; 52(5):2343-51. PubMed ID: 21212183
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Whirlin interacts with espin and modulates its actin-regulatory function: an insight into the mechanism of Usher syndrome type II.
    Wang L; Zou J; Shen Z; Song E; Yang J
    Hum Mol Genet; 2012 Feb; 21(3):692-710. PubMed ID: 22048959
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Current understanding of usher syndrome type II.
    Yang J; Wang L; Song H; Sokolov M
    Front Biosci (Landmark Ed); 2012 Jan; 17(3):1165-83. PubMed ID: 22201796
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ablation of whirlin long isoform disrupts the USH2 protein complex and causes vision and hearing loss.
    Yang J; Liu X; Zhao Y; Adamian M; Pawlyk B; Sun X; McMillan DR; Liberman MC; Li T
    PLoS Genet; 2010 May; 6(5):e1000955. PubMed ID: 20502675
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.