Similar articles for PMID: 24334608

Year	Number of Results
1993	1
1999	2
2003	1
2004	1
2005	4
2006	4
2007	6
2008	5
2009	8
2010	8
2011	8
2012	10
2013	8
2014	9
2015	7
2016	5
2017	11
2018	7
2019	8
2020	4
2021	11
2022	17
2023	10
2024	0

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. Zou J, et al. 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.

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. Chen Q, et al. 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.

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. Du H, et al. FASEB J. 2020 Jan;34(1):1136-1149. doi: 10.1096/fj.201901657RR. Epub 2019 Nov 29. FASEB J. 2020. PMID: 31914662 Free PMC article.

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. Zou J, et al. Hum Mol Genet. 2017 Feb 1;26(3):624-636. doi: 10.1093/hmg/ddw421. Hum Mol Genet. 2017. PMID: 28031293 Free PMC article.

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. Reiners J, et al. Exp Eye Res. 2006 Jul;83(1):97-119. doi: 10.1016/j.exer.2005.11.010. Epub 2006 Mar 20. Exp Eye Res. 2006. PMID: 16545802 Review.

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. Grati M, et al. J Neurosci. 2012 Oct 10;32(41):14288-93. doi: 10.1523/JNEUROSCI.3071-12.2012. J Neurosci. 2012. PMID: 23055499 Free PMC article.

7

Usher protein functions in hair cells and photoreceptors.

Cosgrove D, Zallocchi M. Cosgrove D, et al. Int J Biochem Cell Biol. 2014 Jan;46:80-9. doi: 10.1016/j.biocel.2013.11.001. Epub 2013 Nov 12. Int J Biochem Cell Biol. 2014. PMID: 24239741 Free PMC article. Review.

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. Zou J, et al. 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.

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. Ebermann I, et al. J Clin Invest. 2010 Jun;120(6):1812-23. doi: 10.1172/JCI39715. Epub 2010 May 3. J Clin Invest. 2010. PMID: 20440071 Free PMC article.

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. Sorusch N, et al. Hum Mol Genet. 2017 Mar 15;26(6):1157-1172. doi: 10.1093/hmg/ddx027. Hum Mol Genet. 2017. PMID: 28137943

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