PMC Links for Nucleotide (Select 358001058) - PMC

Select item 63757071.

Zooming in on cadherin-23: Structural diversity and potential mechanisms of inherited deafness

Avinash Jaiganesh, Pedro De-la-Torre, Aniket A. Patel, Domenic J. Termine, Florencia Velez-Cortes, Conghui Chen, Marcos Sotomayor

Structure. Author manuscript; available in PMC 2019 Sep 4.

Published in final edited form as: Structure. 2018 Sep 4; 26(9): 1210–1225.e4. Published online 2018 Jul 19. doi: 10.1016/j.str.2018.06.003

PMCID:: PMC6375707

Abstract Article PDF–4.0M

Select item 14689742.

An inherited kidney disease of mice resembling human nephronophthisis.

M F Lyon, E V Hulse

J Med Genet. 1971 Mar; 8(1): 41–48. doi: 10.1136/jmg.8.1.41

Correction in:: J Med Genet. 1971 Jun; 8(2): 254.

PMCID:: PMC1468974

Summary Page Browse PDF–1.9M

Select item 60900393.

CDH23 Methylation Status and Presbycusis Risk in Elderly Women

Amal Bouzid, Ibtihel Smeti, Amine Chakroun, Salma Loukil, Abdullah Ahmed Gibriel, Mhamed Grati, Abdelmonem Ghorbel, Saber Masmoudi

Front Aging Neurosci. 2018; 10: 241. Published online 2018 Aug 7. doi: 10.3389/fnagi.2018.00241

PMCID:: PMC6090039

Abstract Article PDF–1.2M

Select item 53473804.

Effects of Cdh23 single nucleotide substitutions on age-related hearing loss in C57BL/6 and 129S1/Sv mice and comparisons with congenic strains

Kenneth R. Johnson, Cong Tian, Leona H. Gagnon, Haiyan Jiang, Dalian Ding, Richard Salvi

Sci Rep. 2017; 7: 44450. Published online 2017 Mar 13. doi: 10.1038/srep44450

PMCID:: PMC5347380

Abstract Article PDF–1.0M

Select item 49238615.

Cadherin 23-C Regulates Microtubule Networks by Modifying CAMSAP3’s Function

Satoe Takahashi, Vincent J. Mui, Samuel K. Rosenberg, Kazuaki Homma, Mary Ann Cheatham, Jing Zheng

Sci Rep. 2016; 6: 28706. Published online 2016 Jun 28. doi: 10.1038/srep28706

PMCID:: PMC4923861

Abstract Article PDF–2.3M

Select item 34081396.

Transcriptional Regulation of the Protocadherin β Cluster during Her-2 Protein-induced Mammary Tumorigenesis Results from Altered N-Glycan Branching

Huabei Guo, Alison Nairn, Mitche dela Rosa, Tamas Nagy, Shaying Zhao, Kelley Moremen, Michael Pierce

J Biol Chem. 2012 Jul 20; 287(30): 24941–24954. Published online 2012 Jun 4. doi: 10.1074/jbc.M112.369355

PMCID:: PMC3408139

Abstract Article PDF–2.4M

Select item 30008767.

A new mouse mutant of the Cdh23 gene with early-onset hearing loss facilitates evaluation of otoprotection drugs

Fengchan Han, Heping Yu, Cong Tian, Hui E Chen, Cindy Benedict-Alderfer, Yuxi Zheng, Qiuju Wang, Xu Han, Qing Y Zheng

Pharmacogenomics J. Author manuscript; available in PMC 2012 Aug 1.

Published in final edited form as: Pharmacogenomics J. 2012 Feb; 12(1): 30–44. Published online 2010 Jul 20. doi: 10.1038/tpj.2010.60

PMCID:: PMC3000876

Abstract Article PDF–2.1M

Select item 29898208.

Targeting of the Hair Cell Proteins Cadherin 23, Harmonin, Myosin XVa, Espin, and Prestin in an Epithelial Cell Model

Lili Zheng, Jing Zheng, Donna S. Whitlon, Jaime García-Añoveros, James R. Bartles

J Neurosci. 2010 May 26; 30(21): 7187–7201. doi: 10.1523/JNEUROSCI.0852-10.2010

PMCID:: PMC2989820

Abstract Article PDF–4.5M

Select item 27438059.

Expression of cadherin 23 isoforms is not conserved: implications for a mouse model of Usher syndrome type 1D

Ayala Lagziel, Nora Overlack, Steven L. Bernstein, Robert J. Morell, Uwe Wolfrum, Thomas B. Friedman

Mol Vis. 2009; 15: 1843–1857. Published online 2009 Sep 12.

PMCID:: PMC2743805

Abstract Article PDF–8.3M

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