BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

263 related articles for article (PubMed ID: 28137943)

  • 1. 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]  

  • 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. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis.
    Bauß K; Knapp B; Jores P; Roepman R; Kremer H; Wijk EV; Märker T; Wolfrum U
    Hum Mol Genet; 2014 Aug; 23(15):3923-42. PubMed ID: 24608321
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retina.
    Overlack N; Kilic D; Bauss K; Märker T; Kremer H; van Wijk E; Wolfrum U
    Biochim Biophys Acta; 2011 Oct; 1813(10):1883-92. PubMed ID: 21767579
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Studies of the Periciliary Membrane Complex in the Syrian Hamster Photoreceptor.
    Zou J; Li R; Wang Z; Yang J
    Adv Exp Med Biol; 2019; 1185():543-547. PubMed ID: 31884668
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. [The Usher Syndrome, a Human Ciliopathy].
    Wolfrum U; Nagel-Wolfrum K
    Klin Monbl Augenheilkd; 2018 Mar; 235(3):273-280. PubMed ID: 29534264
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Usher syndrome protein network functions in the retina and their relation to other retinal ciliopathies.
    Sorusch N; Wunderlich K; Bauss K; Nagel-Wolfrum K; Wolfrum U
    Adv Exp Med Biol; 2014; 801():527-33. PubMed ID: 24664740
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Distinct expression and function of whirlin isoforms in the inner ear and retina: an insight into pathogenesis of USH2D and DFNB31.
    Mathur PD; Zou J; Zheng T; Almishaal A; Wang Y; Chen Q; Wang L; Vashist D; Brown S; Park A; Yang J
    Hum Mol Genet; 2015 Nov; 24(21):6213-28. PubMed ID: 26307081
    [TBL] [Abstract][Full Text] [Related]  

  • 18. CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A.
    Testa F; Melillo P; Bonnet C; Marcelli V; de Benedictis A; Colucci R; Gallo B; Kurtenbach A; Rossi S; Marciano E; Auricchio A; Petit C; Zrenner E; Simonelli F
    Retina; 2017 Aug; 37(8):1581-1590. PubMed ID: 27828912
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.
    Khalaileh A; Abu-Diab A; Ben-Yosef T; Raas-Rothschild A; Lerer I; Alswaiti Y; Chowers I; Banin E; Sharon D; Khateb S
    Invest Ophthalmol Vis Sci; 2018 Feb; 59(2):1095-1104. PubMed ID: 29490346
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.