153 related articles for article (PubMed ID: 22892111)
1. The expression of whirlin and Cav1.3α₁ is mutually independent in photoreceptors.
Zou J; Lee A; Yang J
Vision Res; 2012 Dec; 75():53-9. PubMed ID: 22892111
[TBL] [Abstract][Full Text] [Related]
2. Association of whirlin with Cav1.3 (alpha1D) channels in photoreceptors, defining a novel member of the usher protein network.
Kersten FF; van Wijk E; van Reeuwijk J; van der Zwaag B; Märker T; Peters TA; Katsanis N; Wolfrum U; Keunen JE; Roepman R; Kremer H
Invest Ophthalmol Vis Sci; 2010 May; 51(5):2338-46. PubMed ID: 19959638
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Identification of whirlin domains interacting with espin: A study of the mechanism of Usher syndrome type II.
Wang L; Wei B; Fu X; Wang Y; Sui Y; Ma J; Gong X; Hao J; Xing S
Mol Med Rep; 2019 Dec; 20(6):5111-5117. PubMed ID: 31638198
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. RpgrORF15 connects to the usher protein network through direct interactions with multiple whirlin isoforms.
Wright RN; Hong DH; Perkins B
Invest Ophthalmol Vis Sci; 2012 Mar; 53(3):1519-29. PubMed ID: 22323458
[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. 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]
13. 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]
14. 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]
15. 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]
16. 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]
17. The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1.
van Wijk E; van der Zwaag B; Peters T; Zimmermann U; Te Brinke H; Kersten FF; Märker T; Aller E; Hoefsloot LH; Cremers CW; Cremers FP; Wolfrum U; Knipper M; Roepman R; Kremer H
Hum Mol Genet; 2006 Mar; 15(5):751-65. PubMed ID: 16434480
[TBL] [Abstract][Full Text] [Related]
18. Abundant L-type calcium channel Ca(v)1.3 (alpha1D) subunit mRNA is detected in rod photoreceptors of the mouse retina via in situ hybridization.
Xiao H; Chen X; Steele EC
Mol Vis; 2007 May; 13():764-71. PubMed ID: 17563731
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]