Yang J - Search Results

1

Studies of the Periciliary Membrane Complex in the Syrian Hamster Photoreceptor.

Zou J, Li R, Wang Z, Yang J. Zou J, et al. Among authors: yang j. Adv Exp Med Biol. 2019;1185:543-547. doi: 10.1007/978-3-030-27378-1_89. Adv Exp Med Biol. 2019. PMID: 31884668

2

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. Zou J, et al. Among authors: yang j. Invest Ophthalmol Vis Sci. 2011 Apr 12;52(5):2343-51. doi: 10.1167/iovs.10-6141. Print 2011 Apr. Invest Ophthalmol Vis Sci. 2011. PMID: 21212183 Free PMC article.

3

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. Wang L, et al. Among authors: yang j. Hum Mol Genet. 2012 Feb 1;21(3):692-710. doi: 10.1093/hmg/ddr503. Epub 2011 Nov 2. Hum Mol Genet. 2012. PMID: 22048959 Free PMC article.

4

Current understanding of usher syndrome type II.

Yang J, Wang L, Song H, Sokolov M. Yang J, et al. Front Biosci (Landmark Ed). 2012 Jan 1;17(3):1165-83. doi: 10.2741/3979. Front Biosci (Landmark Ed). 2012. PMID: 22201796 Free PMC article.

5

The expression of whirlin and Cav1.3α₁ is mutually independent in photoreceptors.

Zou J, Lee A, Yang J. Zou J, et al. Among authors: yang j. Vision Res. 2012 Dec 15;75:53-9. doi: 10.1016/j.visres.2012.07.020. Epub 2012 Aug 7. Vision Res. 2012. PMID: 22892111 Free PMC article.

6

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. Zou J, et al. Among authors: yang j. Hum Mol Genet. 2014 May 1;23(9):2374-90. doi: 10.1093/hmg/ddt629. Epub 2013 Dec 11. Hum Mol Genet. 2014. PMID: 24334608 Free PMC article.

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. Chen Q, et al. Among authors: yang j. J Biol Chem. 2014 Dec 26;289(52):36070-88. doi: 10.1074/jbc.M114.610535. Epub 2014 Nov 18. J Biol Chem. 2014. PMID: 25406310 Free PMC article.

8

Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Mathur P, Yang J. Mathur P, et al. Among authors: yang j. Biochim Biophys Acta. 2015 Mar;1852(3):406-20. doi: 10.1016/j.bbadis.2014.11.020. Epub 2014 Dec 4. Biochim Biophys Acta. 2015. PMID: 25481835 Free PMC article. Review.

9

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. Mathur PD, et al. Among authors: yang j. Hum Mol Genet. 2015 Nov 1;24(21):6213-28. doi: 10.1093/hmg/ddv339. Epub 2015 Aug 24. Hum Mol Genet. 2015. PMID: 26307081 Free PMC article.

10

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. Zou J, et al. Among authors: yang j. Hum Mol Genet. 2015 Dec 15;24(24):6944-57. doi: 10.1093/hmg/ddv398. Epub 2015 Sep 23. Hum Mol Genet. 2015. PMID: 26401052 Free PMC article.

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