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Select item 101282371.

刘晓宙, 陈森, 孙宇, 孔维佳

Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2021 Mar 5; 35(3): 229-233, 237. Chinese. doi: 10.13201/j.issn.2096-7993.2021.03.008

PMCID:: PMC10128237

Abstract Article PDF–3.7M

Select item 83124412.

Methylation silencing CDH23 is a poor prognostic marker in diffuse large B-cell lymphoma

Baoping Cao, Xiaochuan Guo, Lefu Huang, Bin Wang, Weixia Wang, Dong Han, Weijing Zhang, Kaili Zhong

Aging (Albany NY) 2021 Jul 15; 13(13): 17768–17788. Published online 2021 Jul 12. doi: 10.18632/aging.203268

PMCID:: PMC8312441

Abstract Article PDF–2.2M

Select item 64876933.

The strong propensity of Cadherin‐23 for aggregation inhibits cell migration

Malay K. Sannigrahi, Cheerneni S. Srinivas, Nilesh Deokate, Sabyasachi Rakshit

Mol Oncol. 2019 May; 13(5): 1092–1109. Published online 2019 Mar 19. doi: 10.1002/1878-0261.12469

PMCID:: PMC6487693

Abstract Article PDF–1.9M

Select item 54203494.

Germline Mutations in CDH23, Encoding Cadherin-Related 23, Are Associated with Both Familial and Sporadic Pituitary Adenomas

Qilin Zhang, Cheng Peng, Jianping Song, Yichao Zhang, Jianhua Chen, Zhijian Song, Xuefei Shou, Zengyi Ma, Hong Peng, Xuemin Jian, Wenqiang He, Zhao Ye, Zhiqiang Li, Yongfei Wang, Hongying Ye, Zhaoyun Zhang, Ming Shen, Feng Tang, Hong Chen, Zhifeng Shi, Chunjui Chen, Zhengyuan Chen, Yue Shen, Ye Wang, Shaoyong Lu, Jian Zhang, Yiming Li, Shiqi Li, Ying Mao, Liangfu Zhou, Hai Yan, Yongyong Shi, Chuanxin Huang, Yao Zhao

Am J Hum Genet. 2017 May 4; 100(5): 817–823. Published online 2017 Apr 13. doi: 10.1016/j.ajhg.2017.03.011

PMCID:: PMC5420349

Abstract Article PDF–1.8M

Select item 50850945.

Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans

Bong Jik Kim, Ah Reum Kim, Chung Lee, So Young Kim, Nayoung K. D. Kim, Mun Young Chang, Jihye Rhee, Mi-Hyun Park, Soo Kyung Koo, Min Young Kim, Jin Hee Han, Seung-ha Oh, Woong-Yang Park, Byung Yoon Choi

PLoS One. 2016; 11(10): e0165680. Published online 2016 Oct 28. doi: 10.1371/journal.pone.0165680

PMCID:: PMC5085094

Abstract Article PDF–2.4M

Select item 45341056.

Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric population

So Young Kim, Ah Reum Kim, Nayoung K D Kim, Min Young Kim, Eun-Hee Jeon, Bong Jik Kim, Young Eun Han, Mun Young Chang, Woong-Yang Park, Byung Yoon Choi

J Transl Med. 2015; 13: 263. Published online 2015 Aug 13. doi: 10.1186/s12967-015-0624-8

PMCID:: PMC4534105

Abstract Article PDF–3.3M

Select item 44517187.

High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss

Kunio Mizutari, Hideki Mutai, Kazunori Namba, Yuko Miyanaga, Atsuko Nakano, Yukiko Arimoto, Sawako Masuda, Noriko Morimoto, Hirokazu Sakamoto, Kimitaka Kaga, Tatsuo Matsunaga

Orphanet J Rare Dis. 2015; 10: 60. Published online 2015 May 13. doi: 10.1186/s13023-015-0276-z

PMCID:: PMC4451718

Abstract Article PDF–879K

Select item 40364258.

Identification of CDH23 mutations in Korean families with hearing loss by whole-exome sequencing

Hae-Mi Woo, Hong-Joon Park, Mi-Hyun Park, Bo-Young Kim, Joong-Wook Shin, Won Gi Yoo, Soo Kyung Koo

BMC Med Genet. 2014; 15: 46. Published online 2014 Apr 28. doi: 10.1186/1471-2350-15-46

PMCID:: PMC4036425

Abstract Article PDF–867K

Select item 34168299.

Prevalence and Clinical Features of Hearing Loss Patients with CDH23 Mutations: A Large Cohort Study

Maiko Miyagawa, Shin-ya Nishio, Shin-ichi Usami

PLoS One. 2012; 7(8): e40366. Published online 2012 Aug 10. doi: 10.1371/journal.pone.0040366

PMCID:: PMC3416829

Abstract Article PDF–762K

Select item 329668910.

Cadherin-23 Mediates Heterotypic Cell-Cell Adhesion between Breast Cancer Epithelial Cells and Fibroblasts

Maria Apostolopoulou, Lee Ligon

PLoS One. 2012; 7(3): e33289. Published online 2012 Mar 7. doi: 10.1371/journal.pone.0033289

PMCID:: PMC3296689

Abstract Article PDF–2.8M

Select item 239989511.

Mutation Profile of the CDH23 Gene in 56 Probands with Usher Syndrome Type I

A. Oshima, T. Jaijo, E. Aller, J.M. Millan, C. Carney, S. Usami, C. Moller, W.J. Kimberling

Hum Mutat. Author manuscript; available in PMC 2009 Jun 1.

Published in final edited form as: Hum Mutat. 2008 Jun; 29(6): E37–E46. doi: 10.1002/humu.20761

PMCID:: PMC2399895

Abstract Article PDF–305K

Select item 37915912.

CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

L. M. Astuto, J. M. Bork, M. D. Weston, J. W. Askew, R. R. Fields, D. J. Orten, S. J. Ohliger, S. Riazuddin, R. J. Morell, S. Khan, S. Riazuddin, H. Kremer, P. van Hauwe, C. G. Moller, C. W. R. J. Cremers, C. Ayuso, J. R. Heckenlively, K. Rohrschneider, U. Spandau, J. Greenberg, R. Ramesar, W. Reardon, P. Bitoun, J. Millan, R. Legge, T. B. Friedman, W. J. Kimberling

Am J Hum Genet. 2002 Aug; 71(2): 262–275. Published online 2002 Jun 19. doi: 10.1086/341558

PMCID:: PMC379159

Abstract Article PDF–562K

Select item 776756813.

Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, Masoud Garshasbi

Mol Genet Genomic Med. 2020 Dec; 8(12): e1550. Published online 2020 Nov 18. doi: 10.1002/mgg3.1550

PMCID:: PMC7767568

Abstract Article PDF–1.9M

Select item 637570714.

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 358144615.

Study of USH1 Splicing Variants through Minigenes and Transcript Analysis from Nasal Epithelial Cells

María José Aparisi, Gema García-García, Elena Aller, María Dolores Sequedo, Cristina Martínez-Fernández de la Cámara, Regina Rodrigo, Miguel Armengot, Julio Cortijo, Javier Milara, Manuel Díaz-LLopis, Teresa Jaijo, José María Millán

PLoS One. 2013; 8(2): e57506. Published online 2013 Feb 25. doi: 10.1371/journal.pone.0057506

PMCID:: PMC3581446

Abstract Article PDF–446K

Select item 346044716.

Large Protein Assemblies Formed by Multivalent Interactions between Cadherin23 and Harmonin Suggest a Stable Anchorage Structure at the Tip Link of Stereocilia

Lin Wu, Lifeng Pan, Chuchu Zhang, Mingjie Zhang

J Biol Chem. 2012 Sep 28; 287(40): 33460–33471. Published online 2012 Aug 8. doi: 10.1074/jbc.M112.378505

PMCID:: PMC3460447

Abstract Article PDF–3.8M

Select item 266705217.

Assembling stable hair cell tip link complex via multidentate interactions between harmonin and cadherin 23

Lifeng Pan, Jing Yan, Lin Wu, Mingjie Zhang

Proc Natl Acad Sci U S A. 2009 Apr 7; 106(14): 5575–5580. Published online 2009 Mar 18. doi: 10.1073/pnas.0901819106

PMCID:: PMC2667052

Abstract Article PDF–958K

Select item 123492318.

Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23

Julie M. Bork, Linda M. Peters, Saima Riazuddin, Steve L. Bernstein, Zubair M. Ahmed, Seth L. Ness, Robert Polomeno, Arabandi Ramesh, Melvin Schloss, C. R. Srikumari Srisailpathy, Sigrid Wayne, Susan Bellman, Dilip Desmukh, Zahoor Ahmed, Shaheen N. Khan, Vazken M. Der Kaloustian, X. Cindy Li, Anil Lalwani, Sheikh Riazuddin, Maria Bitner-Glindzicz, Walter E. Nance, Xue-Zhong Liu, Graeme Wistow, Richard J. H. Smith, Andrew J. Griffith, Edward R. Wilcox, Thomas B. Friedman, Robert J. Morell

Am J Hum Genet. 2001 Jan; 68(1): 26–37. Published online 2000 Nov 21. doi: 10.1086/316954

PMCID:: PMC1234923

Abstract Article PDF–818K

Select item 1107896919.

Comparison of vestibular function in hereditary hearing loss patients with GJB2, CDH23, and SLC26A4 variants

Keita Tsukada, Shin-ya Nishio, Yutaka Takumi, Shin-ichi Usami

Sci Rep. 2024; 14: 10596. Published online 2024 May 8. doi: 10.1038/s41598-024-61442-3

PMCID:: PMC11078969

Abstract Article PDF–1.2M

Select item 723056220.

High-Throughput Sequencing Identifies 3 Novel Susceptibility Genes for Hereditary Melanoma

Catarina Campos, Sofia Fragoso, Rafael Luís, Filipe Pinto, Cheila Brito, Susana Esteves, Margarida Pataco, Sidónia Santos, Patrícia Machado, João B. Vicente, Joaninha Costa Rosa, Branca M. Cavaco, Cecília Moura, Marta Pojo

Genes (Basel) 2020 Apr; 11(4): 403. Published online 2020 Apr 8. doi: 10.3390/genes11040403

PMCID:: PMC7230562

Abstract Article PDF–2.7M

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