U.S. flag

An official website of the United States government

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from GEO Profiles

Items: 1 to 20 of 79

1.
The association of genetic polymorphisms in protocadherin 15 with sudden sensorineural hearing loss in a Chinese population
Ying Lan, Tao Hou, Lu Peng, Yongpeng Li, Shihua Yin
J Clin Lab Anal. 2023 Apr; 37(8): e24896. Published online 2023 May 17. doi: 10.1002/jcla.24896
PMCID:
PMC10290222
AbstractArticlePDF–258K
2.
Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways
Yilan Zhen, Carlie L. Cullen, Raphael Ricci, Benjamin S. Summers, Sakina Rehman, Zubair M. Ahmed, Antoinette Y. Foster, Ben Emery, Robert Gasperini, Kaylene M. Young
Commun Biol. 2022; 5: 511. Published online 2022 May 30. doi: 10.1038/s42003-022-03470-1
PMCID:
PMC9151716
AbstractArticlePDF–13M
3.
Structural determinants of protocadherin-15 mechanics and function in hearing and balance perception
Deepanshu Choudhary, Yoshie Narui, Brandon L. Neel, Lahiru N. Wimalasena, Carissa F. Klanseck, Pedro De-la-Torre, Conghui Chen, Raul Araya-Secchi, Elakkiya Tamilselvan, Marcos Sotomayor
Proc Natl Acad Sci U S A. 2020 Oct 6; 117(40): 24837–24848. Published online 2020 Sep 22. doi: 10.1073/pnas.1920444117
PMCID:
PMC7547225
AbstractArticlePDF–5.1M
4.
The Tip-Link Antigen, a Protein Associated with the Transduction Complex of Sensory Hair Cells, Is Protocadherin-15
Zubair M. Ahmed, Richard Goodyear, Saima Riazuddin, Ayala Lagziel, P. Kevin Legan, Martine Behra, Shawn M. Burgess, Kathryn S. Lilley, Edward R. Wilcox, Sheikh Riazuddin, Andrew J. Griffith, Gregory I. Frolenkov, Inna A. Belyantseva, Guy P. Richardson, Thomas B. Friedman
J Neurosci. 2006 Jun 28; 26(26): 7022–7034. doi: 10.1523/JNEUROSCI.1163-06.2006
PMCID:
PMC6673907
AbstractArticlePDF–1.0M
5.
Mechanotransduction by Pcdh15 relies on a novel cis-dimeric architecture
Gilman Dionne, Xufeng Qiu, Micah Rapp, Xiaoping Liang, Bo Zhao, Guihong Peng, Phinikoula S. Katsamba, Goran Ahlsen, Rotem Rubinstein, Clinton S. Potter, Bridget Carragher, Barry Honig, Ulrich Müller, Lawrence Shapiro
Neuron. Author manuscript; available in PMC 2018 Oct 2.
Published in final edited form as: Neuron. 2018 Aug 8; 99(3): 480–492.e5. Published online 2018 Jul 26. doi: 10.1016/j.neuron.2018.07.006
PMCID:
PMC6168201
AbstractArticlePDF–1.5M
6.
Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment
Isabelle Schrauwen, Imen Chakchouk, Anushree Acharya, Khurram Liaqat, Irfanullah, University of Washington Center for Mendelian Genomics, Deborah A. Nickerson, Michael J. Bamshad, Khadim Shah, Wasim Ahmad, Suzanne M. Leal
BMC Med Genet. 2018; 19: 122. Published online 2018 Jul 20. doi: 10.1186/s12881-018-0618-5
PMCID:
PMC6053831
AbstractArticlePDF–752K
7.
Identification of Pathogenic Genes of Nonsyndromic Hearing Loss in Uyghur Families Using Massively Parallel DNA Sequencing Technique
Yu Chen, Yu Lu, Pilidong Kuyaxi, Jing Cheng, Juan Zhao, Qi Zhao, Patiguli Musha, Hua Zhang, Huijun Yuan
Dis Markers. 2018; 2018: 5298057. Published online 2018 Mar 5. doi: 10.1155/2018/5298057
PMCID:
PMC5859828
AbstractArticlePDF–4.6M
8.
Genetics of the human face: Identification of large-effect single gene variants
Daniel J. M. Crouch, Bruce Winney, Willem P. Koppen, William J. Christmas, Katarzyna Hutnik, Tammy Day, Devendra Meena, Abdelhamid Boumertit, Pirro Hysi, Ayrun Nessa, Tim D. Spector, Josef Kittler, Walter F. Bodmer
Proc Natl Acad Sci U S A. 2018 Jan 23; 115(4): E676–E685. Published online 2018 Jan 4. doi: 10.1073/pnas.1708207114
PMCID:
PMC5789906
AbstractArticlePDF–1.4M
9.
Discovery of novel plasma proteins as biomarkers for the development of incisional hernias after midline incision in colorectal cancer patients: the ColoCare Study
Jürgen Böhm, Frank Pianka, Nina Stüttgen, Junghyun Rho, Biljana Gigic, Yuzheng Zhang, Nina Habermann, Petra Schrotz-King, Clare Abbenhardt-Martin, Lin Zielske, Paul D. Lampe, Alexis Ulrich, Markus Diener, Cornelia M. Ulrich
Surgery. Author manuscript; available in PMC 2018 Mar 1.
Published in final edited form as: Surgery. 2017 Mar; 161(3): 808–817. Published online 2016 Oct 13. doi: 10.1016/j.surg.2016.08.025
PMCID:
PMC5560863
AbstractArticlePDF–805K
10.
Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss
Rongrong Wang, Shirui Han, Amjad Khan, Xue Zhang
Genet Test Mol Biomarkers. 2017 May 1; 21(5): 316–321. Published online 2017 May 1. doi: 10.1089/gtmb.2016.0328
PMCID:
PMC5444417
AbstractArticlePDF–307K
11.
A partial calcium-free linker confers flexibility to inner-ear protocadherin-15
Robert E. Powers, Rachelle Gaudet, Marcos Sotomayor
Structure. Author manuscript; available in PMC 2018 Mar 7.
Published in final edited form as: Structure. 2017 Mar 7; 25(3): 482–495. Published online 2017 Feb 23. doi: 10.1016/j.str.2017.01.014
PMCID:
PMC5363953
AbstractArticlePDF–1.6M
12.
Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders
Min-Tzu Lo, David A. Hinds, Joyce Y. Tung, Carol Franz, Chun-Chieh Fan, Yunpeng Wang, Olav B. Smeland, Andrew Schork, Dominic Holland, Karolina Kauppi, Nilotpal Sanyal, Valentina Escott-Price, Daniel J. Smith, Michael O'Donovan, Hreinn Stefansson, Gyda Bjornsdottir, Thorgeir E. Thorgeirsson, Kari Stefansson, Linda K. McEvoy, Anders M. Dale, Ole A. Andreassen, Chi-Hua Chen
Nat Genet. Author manuscript; available in PMC 2017 Jan 30.
Published in final edited form as: Nat Genet. 2017 Jan; 49(1): 152–156. Published online 2016 Dec 5. doi: 10.1038/ng.3736
PMCID:
PMC5278898
AbstractArticlePDF–1.6M
13.
Plasma Membrane Targeting of Protocadherin 15 Is Regulated by the Golgi-Associated Chaperone Protein PIST
Hongyun Nie, Yueyue Liu, Xiaolei Yin, Huiren Cao, Yanfei Wang, Wei Xiong, Yushuang Lin, Zhigang Xu
Neural Plast. 2016; 2016: 8580675. Published online 2016 Oct 27. doi: 10.1155/2016/8580675
PMCID:
PMC5102745
AbstractArticlePDF–5.0M
14.
Utilization of amplicon-based targeted sequencing panel for the massively parallel sequencing of sporadic hearing impairment patients from Saudi Arabia
Ashraf Dallol, Kamal Daghistani, Aisha Elaimi, Wissam A. Al-Wazani, Afaf Bamanie, Malek Safiah, Samira Sagaty, Layla Taha, Rawabi Zahed, Osama Bajouh, Adeel Gulzar Chaudhary, Mamdooh Abdullah Gari, Rola Turki, Mohammed Hussein Al-Qahtani, Adel Mohammed Abuzenadah
BMC Med Genet. 2016; 17(Suppl 1): 67. Published online 2016 Oct 10. doi: 10.1186/s12881-016-0329-8
PMCID:
PMC5073994
AbstractArticlePDF–547K
15.
Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome
Samia Abdi, Amel Bahloul, Asma Behlouli, Jean-Pierre Hardelin, Mohamed Makrelouf, Kamel Boudjelida, Malek Louha, Ahmed Cheknene, Rachid Belouni, Yahia Rous, Zahida Merad, Djamel Selmane, Mokhtar Hasbelaoui, Crystel Bonnet, Akila Zenati, Christine Petit
PLoS One. 2016; 11(9): e0161893. Published online 2016 Sep 1. doi: 10.1371/journal.pone.0161893
PMCID:
PMC5008642
AbstractArticlePDF–1.7M
16.
Genetic analysis of Tunisian families with Usher syndrome type 1: toward improving early molecular diagnosis
Imen Ben-Rebeh, Mhamed Grati, Crystel Bonnet, Walid Bouassida, Imen Hadjamor, Hammadi Ayadi, Abdelmonem Ghorbel, Christine Petit, Saber Masmoudi
Mol Vis. 2016; 22: 827–835. Published online 2016 Jul 19.
PMCID:
PMC4950652
AbstractArticlePDF–949K
17.
Independent validation of a mathematical genomic model for survival of glioma patients
Jason B Nikas
Am J Cancer Res. 2016; 6(6): 1408–1419. Published online 2016 Jun 1.
PMCID:
PMC4937742
AbstractArticlePDF–1.0M
18.
Frequency of Usher syndrome type 1 in deaf children by massively parallel DNA sequencing
Hidekane Yoshimura, Maiko Miyagawa, Kozo Kumakawa, Shin-ya Nishio, Shin-ichi Usami
J Hum Genet. 2016 May; 61(5): 419–422. Published online 2016 Jan 21. doi: 10.1038/jhg.2015.168
PMCID:
PMC4893503
AbstractArticlePDF–330K
19.
In silico analysis of a disease-causing mutation in PCDH15 gene in a consanguineous Pakistani family with Usher phenotype
Shamim Saleha, Muhammad Ajmal, Muhammad Jamil, Muhammad Nasir, Abdul Hameed
Int J Ophthalmol. 2016; 9(5): 662–668. Published online 2016 May 18. doi: 10.18240/ijo.2016.05.04
PMCID:
PMC4886895
AbstractArticlePDF–1021K
20.
MYO3A causes human dominant deafness and interacts with protocadherin 15-CD2 isoform
M’hamed Grati, Denise Yan, Manmeet H. Raval, Tom Walsh, Qi Ma, Imen Chakchouk, Abhiraami Kannan-Sundhari, Rahul Mittal, Saber Masmoudi, Susan H. Blanton, Mustafa Tekin, Mary-Claire King, Christopher M. Yengo, Xue Zhong Liu
Hum Mutat. Author manuscript; available in PMC 2017 May 1.
Published in final edited form as: Hum Mutat. 2016 May; 37(5): 481–487. Published online 2016 Feb 16. doi: 10.1002/humu.22961
PMCID:
PMC4833613
AbstractArticlePDF–819K

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center