BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 31884668)

  • 1. 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]  

  • 2. Usherin defects lead to early-onset retinal dysfunction in zebrafish.
    Dona M; Slijkerman R; Lerner K; Broekman S; Wegner J; Howat T; Peters T; Hetterschijt L; Boon N; de Vrieze E; Sorusch N; Wolfrum U; Kremer H; Neuhauss S; Zang J; Kamermans M; Westerfield M; Phillips J; van Wijk E
    Exp Eye Res; 2018 Aug; 173():148-159. PubMed ID: 29777677
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Genetics, pathogenesis and therapeutic developments for Usher syndrome type 2.
    Stemerdink M; García-Bohórquez B; Schellens R; Garcia-Garcia G; Van Wijk E; Millan JM
    Hum Genet; 2022 Apr; 141(3-4):737-758. PubMed ID: 34331125
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. 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]  

  • 9. Affinity purification of in vivo assembled whirlin-associated protein complexes from the zebrafish retina.
    Schellens RTW; Slijkerman RWN; Hetterschijt L; Peters TA; Broekman S; Clemént A; Westerfield M; Phillips JB; Boldt K; Kremer H; De Vrieze E; Van Wijk E
    J Proteomics; 2022 Aug; 266():104666. PubMed ID: 35788411
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy.
    Han S; Liu X; Xie S; Gao M; Liu F; Yu S; Sun P; Wang C; Archacki S; Lu Z; Hu X; Qin Y; Qu Z; Huang Y; Lv Y; Tu J; Li J; Yimer TA; Jiang T; Tang Z; Luo D; Chen F; Liu M
    Hum Genet; 2018 Oct; 137(10):779-794. PubMed ID: 30242501
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Auditory and olfactory findings in patients with USH2A-related retinal degeneration-Findings at baseline from the rate of progression in USH2A-related retinal degeneration natural history study (RUSH2A).
    Iannaccone A; Brewer CC; Cheng P; Duncan JL; Maguire MG; Audo I; Ayala AR; Bernstein PS; Bidelman GM; Cheetham JK; Doty RL; Durham TA; Hufnagel RB; Myers MH; Stingl K; Zein WM;
    Am J Med Genet A; 2021 Dec; 185(12):3717-3727. PubMed ID: 34331386
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2.
    Kaiserman N; Obolensky A; Banin E; Sharon D
    Arch Ophthalmol; 2007 Feb; 125(2):219-24. PubMed ID: 17296898
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews.
    Auslender N; Bandah D; Rizel L; Behar DM; Shohat M; Banin E; Allon-Shalev S; Sharony R; Sharon D; Ben-Yosef T
    Genet Test; 2008 Jun; 12(2):289-94. PubMed ID: 18452394
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1.
    Tebbe L; Mwoyosvi ML; Crane R; Makia MS; Kakakhel M; Cosgrove D; Al-Ubaidi MR; Naash MI
    Nat Commun; 2023 Feb; 14(1):972. PubMed ID: 36810733
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The effects of ush2a gene knockout on vesicle transport in photoreceptors.
    Han S; Wang Q; Cheng M; Hu Y; Liu P; Hou W; Liang L
    Gene; 2024 Jan; 892():147885. PubMed ID: 37813209
    [TBL] [Abstract][Full Text] [Related]  

  • 20. USH2A Gene Mutations in Rabbits Lead to Progressive Retinal Degeneration and Hearing Loss.
    Nguyen VP; Song J; Prieskorn D; Zou J; Li Y; Dolan D; Xu J; Zhang J; Jayasundera KT; Yang J; Raphael Y; Khan N; Iannuzzi M; Bisgaier C; Chen YE; Paulus YM; Yang D
    Transl Vis Sci Technol; 2023 Feb; 12(2):26. PubMed ID: 36795064
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.