PMC Links for GEO Profiles (Select 94263181) - PMC

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

Abstract Article PDF–13M

Select item 75472255.

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

Abstract Article PDF–5.1M

Select item 66739076.

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

Abstract Article PDF–1.0M

Select item 61682017.

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

Abstract Article PDF–1.5M

Select item 60538318.

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

Abstract Article PDF–752K

Select item 58598289.

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

Abstract Article PDF–4.6M

Select item 578990610.

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

Abstract Article PDF–1.4M

Select item 556086311.

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

Abstract Article PDF–805K

Select item 544441712.

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

Abstract Article PDF–307K

Select item 536395313.

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

Abstract Article PDF–1.6M

Select item 527889814.

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

Abstract Article PDF–1.6M

Select item 510274515.

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

Abstract Article PDF–5.0M

Select item 507399416.

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

Abstract Article PDF–547K

Select item 500864217.

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

Abstract Article PDF–1.7M

Select item 495065218.

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

Abstract Article PDF–949K

Select item 493774219.

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

Abstract Article PDF–1.0M

Select item 489350320.

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

Abstract Article PDF–330K

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