PMC Links for Gene (Select 690865) - PMC

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Items: 14

Select item 30624281.

Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain

Stuart W. Webb, Nicolas Grillet, Leonardo R. Andrade, Wei Xiong, Lani Swarthout, Charley C. Della Santina, Bechara Kachar, Ulrich Müller

Development. 2011 Apr 15; 138(8): 1607–1617. doi: 10.1242/dev.060061

PMCID:: PMC3062428

Abstract Article

Select item 28553062.

A new spontaneous mutation in the mouse protocadherin 15 gene

Q.Y. Zheng, H Yu, J.L. Washington, III, L.B. Kisley, Y.S. Kikkawa, K.S. Pawlowski, C.G. Wright, K.N. Alagramam

Hear Res. Author manuscript; available in PMC 2010 Apr 15.

Published in final edited form as: Hear Res. 2006 Sep; 219(1-2): 110–120. Published online 2006 Aug 2. doi: 10.1016/j.heares.2006.06.010

PMCID:: PMC2855306

Abstract Article PDF–2.1M

Select item 26319813.

Calcium-dependent Binding of HCN1 Channel Protein to Hair Cell Stereociliary Tip Link Protein Protocadherin 15 CD3

Neeliyath A. Ramakrishnan, Marian J. Drescher, Roberto L. Barretto, Kirk W. Beisel, James S. Hatfield, Dennis G. Drescher

J Biol Chem. 2009 Jan 30; 284(5): 3227–3238. doi: 10.1074/jbc.M806177200

PMCID:: PMC2631981

Abstract Article PDF–856K

Select item 33109594.

SENSING SOUND: MOLECULES THAT ORCHESTRATE MECHANOTRANSDUCTION BY HAIR CELLS

Piotr Kazmierczak, Ulrich Müller

Trends Neurosci. Author manuscript; available in PMC 2013 Apr 1.

Published in final edited form as: Trends Neurosci. 2012 Apr; 35(4): 220–229. Published online 2011 Dec 15. doi: 10.1016/j.tins.2011.10.007

PMCID:: PMC3310959

Abstract Article PDF–2.2M

Select item 25645785.

Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%

A‐F Roux, V Faugère, S Le Guédard, N Pallares‐Ruiz, A Vielle, S Chambert, S Marlin, C Hamel, B Gilbert, S Malcolm, M Claustres

J Med Genet. 2006 Sep; 43(9): 763–768. Published online 2006 Apr 5. doi: 10.1136/jmg.2006.041954

PMCID:: PMC2564578

Abstract Article PDF–198K

Select item 28582226.

Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans

Qing Yin Zheng, Denise Yan, Xiao Mei Ouyang, Li Lin Du, Heping Yu, Bo Chang, Kenneth R. Johnson, Xue Zhong Liu

Hum Mol Genet. Author manuscript; available in PMC 2010 Apr 21.

Published in final edited form as: Hum Mol Genet. 2005 Jan 1; 14(1): 103–111. Published online 2004 Nov 10. doi: 10.1093/hmg/ddi010

PMCID:: PMC2858222

Abstract Article PDF–2.2M

Select item 34880417.

HCN1 and HCN2 Proteins Are Expressed in Cochlear Hair Cells: HCN1 CAN FORM A TERNARY COMPLEX WITH PROTOCADHERIN 15 CD3 AND F-ACTIN-BINDING FILAMIN A OR CAN INTERACT WITH HCN2

Neeliyath A. Ramakrishnan, Marian J. Drescher, Khalid M. Khan, James S. Hatfield, Dennis G. Drescher

J Biol Chem. 2012 Nov 2; 287(45): 37628–37646. Published online 2012 Sep 4. doi: 10.1074/jbc.M112.375832

PMCID:: PMC3488041

Abstract Article PDF–4.2M

Select item 27128358.

Physical and Functional Interaction between Protocadherin 15 and Myosin VIIa in Mechanosensory Hair Cells

Mathias Senften, Martin Schwander, Piotr Kazmierczak, Concepcion Lillo, Jung-Bum Shin, Tama Hasson, Gwenaëlle S. G. Géléoc, Peter G. Gillespie, David Williams, Jeffrey R. Holt, Ulrich Müller

J Neurosci. 2006 Feb 15; 26(7): 2060–2071. doi: 10.1523/JNEUROSCI.4251-05.2006

PMCID:: PMC2712835

Abstract Article PDF–943K

Select item 14606929.

A new mouse insertional mutation that causes sensorineural deafness and vestibular defects.

K N Alagramam, H Y Kwon, N L Cacheiro, L Stubbs, C G Wright, L C Erway, R P Woychik

Genetics. 1999 Aug; 152(4): 1691–1699. doi: 10.1093/genetics/152.4.1691

PMCID:: PMC1460692

Summary PDF–332K

Select item 288851610.

Mechanotransduction by Hair Cells: Models, Molecules, and Mechanisms

Peter G. Gillespie, Ulrich Müller

Cell. Author manuscript; available in PMC 2010 Jun 21.

Published in final edited form as: Cell. 2009 Oct 2; 139(1): 33–44. doi: 10.1016/j.cell.2009.09.010

PMCID:: PMC2888516

Abstract Article PDF–3.7M

Select item 122604511.

Mutations of the Protocadherin Gene PCDH15 Cause Usher Syndrome Type 1F

Zubair M. Ahmed, Saima Riazuddin, Steve L. Bernstein, Zahoor Ahmed, Shaheen Khan, Andrew J. Griffith, Robert J. Morell, Thomas B. Friedman, Sheikh Riazuddin, Edward R. Wilcox

Am J Hum Genet. 2001 Jul; 69(1): 25–34. Published online 2001 Jun 7. doi: 10.1086/321277

PMCID:: PMC1226045

Abstract Article PDF–273K

Select item 352217812.

TMHS is an Integral Component of the Mechanotransduction Machinery of Cochlear Hair Cells

Wei Xiong, Nicolas Grillet, Heather M. Elledge, Thomas F.J. Wagner, Bo Zhao, Kenneth R. Johnson, Piotr Kazmierczak, Ulrich Müller

Cell. Author manuscript; available in PMC 2013 Dec 7.

Published in final edited form as: Cell. 2012 Dec 7; 151(6): 1283–1295. doi: 10.1016/j.cell.2012.10.041

PMCID:: PMC3522178

Abstract Article PDF–2.7M

Select item 473838613.

Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth

Andrea Lelli, Vincent Michel, Jacques Boutet de Monvel, Matteo Cortese, Montserrat Bosch-Grau, Asadollah Aghaie, Isabelle Perfettini, Typhaine Dupont, Paul Avan, Aziz El-Amraoui, Christine Petit

J Cell Biol. 2016 Jan 18; 212(2): 231–244. doi: 10.1083/jcb.201509017