PMC Links for Gene (Select 7007) - PMC

Links from Gene

Items: 1 to 20 of 23

<< First< Prev

Page of 2

Select item 56133821.

Prevalence of TECTA mutation in patients with mid-frequency sensorineural hearing loss

Nobuko Yamamoto, Hideki Mutai, Kazunori Namba, Noriko Morita, Shin Masuda, Yasuyuki Nishi, Atsuko Nakano, Sawako Masuda, Masato Fujioka, Kimitaka Kaga, Kaoru Ogawa, Tatsuo Matsunaga

Orphanet J Rare Dis. 2017; 12: 157. Published online 2017 Sep 25. doi: 10.1186/s13023-017-0708-z

PMCID:: PMC5613382

Abstract Article PDF–2.2M

Select item 40162312.

Whole-Exome Sequencing Identifies a Novel Genotype-Phenotype Correlation in the Entactin Domain of the Known Deafness Gene TECTA

Byung Yoon Choi, Jiwoong Kim, Juyong Chung, Ah Reum Kim, Sue Jean Mun, Seong Il Kang, Sang-Heon Lee, Namshin Kim, Seung-Ha Oh

PLoS One. 2014; 9(5): e97040. Published online 2014 May 9. doi: 10.1371/journal.pone.0097040

PMCID:: PMC4016231

Abstract Article PDF–830K

Select item 39949663.

A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family

Haihua Bai, Xukui Yang, Temuribagen, Guilan, Suyalatu, Narisu Narisu, Huiguang Wu, Yujie Chen, Yangjian Liu, Qizhu Wu

BMC Med Genet. 2014; 15: 34. Published online 2014 Mar 19. doi: 10.1186/1471-2350-15-34

PMCID:: PMC3994966

Abstract Article PDF–1.9M

Select item 37295594.

Identification of a Novel TECTA Mutation in a Chinese DFNA8/12 Family with Prelingual Progressive Sensorineural Hearing Impairment

Zhengyue Li, Yilian Guo, Yu Lu, Jianzhong Li, Zhanguo Jin, Hongbo Li, Yanping Lu, Pu Dai, Dongyi Han, Jing Cheng, Huijun Yuan

PLoS One. 2013; 8(7): e70134. Published online 2013 Jul 31. doi: 10.1371/journal.pone.0070134

PMCID:: PMC3729559

Abstract Article PDF–522K

Select item 33266655.

DFNA8/12 Caused by TECTA Mutations is the Most Identified Subtype of Non-syndromic Autosomal Dominant Hearing Loss

Michael S. Hildebrand, Matías Morín, Nicole C. Meyer, Fernando Mayo, Silvia Modamio-Hoybjor, Angeles Mencía, Leticia Olavarrieta, Carmelo Morales-Angulo, Carla J. Nishimura, Heather Workman, Adam P. DeLuca, Ignacio del Castillo, Kyle R. Taylor, Bruce Tompkins, Corey W. Goodman, Isabelle Schrauwen, Maarten Van Wesemael, K. Lachlan, A. Eliot Shearer, Terry A. Braun, Patrick L.M. Huygen, Hannie Kremer, Guy Van Camp, Felipe Moreno, Thomas L. Casavant, Richard J.H. Smith, Miguel A. Moreno-Pelayo

Hum Mutat. Author manuscript; available in PMC 2012 Apr 16.

Published in final edited form as: Hum Mutat. 2011 Jul; 32(7): 825–834. Published online 2011 Jun 7. doi: 10.1002/humu.21512

PMCID:: PMC3326665

Abstract Article PDF–1.8M

Select item 25384176.

Audiological Evaluation of Affected Members from a Dutch DFNA8/12 (TECTA) Family

Rutger F. Plantinga, Cor W.R.J. Cremers, Patrick L.M. Huygen, Henricus P.M. Kunst, Arjan J. Bosman

J Assoc Res Otolaryngol. 2007 Mar; 8(1): 1–7. Published online 2006 Nov 30. doi: 10.1007/s10162-006-0060-9

PMCID:: PMC2538417

Abstract Article PDF–311K

Select item 25045777.

A Novel TECTA Mutation in a Dutch DFNA8/12 Family Confirms Genotype–Phenotype Correlation

Rutger F. Plantinga, Arjan P.M. de Brouwer, Patrick L.M. Huygen, Henricus P.M. Kunst, Hannie Kremer, Cor W.R.J. Cremers

J Assoc Res Otolaryngol. 2006 Jun; 7(2): 173–181. Published online 2006 Apr 25. doi: 10.1007/s10162-006-0033-z

PMCID:: PMC2504577

Abstract Article PDF–364K

Select item 17354548.

Distinctive audiometric profile associated with DFNB21 alleles of TECTA

S Naz, F Alasti, A Mowjoodi, S Riazuddin, M Sanati, T Friedman, A Griffith, E Wilcox, S Riazuddin

J Med Genet. 2003 May; 40(5): 360–363. doi: 10.1136/jmg.40.5.360

PMCID:: PMC1735454

Summary PDF–243K

Select item 17348709.

A cysteine substitution in the zona pellucida domain of α-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family

M. A. Moreno-Pelayo, I. del Castillo, M. Villamar, L. Romero, F. J. Hernandez-Calvin, C. Herraiz, R. Barbera, C. Navas, F. Moreno

J Med Genet. 2001 May; 38(5): e13. doi: 10.1136/jmg.38.5.e13

PMCID:: PMC1734870

Summary PDF–125K

Select item 171244010.

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

K Verhoeven, G Van Camp, P J Govaerts, W Balemans, I Schatteman, M Verstreken, L Van Laer, R J Smith, M R Brown, P H Van de Heyning, T Somers, F E Offeciers, P J Willems

Am J Hum Genet. 1997 May; 60(5): 1168–1173.

PMCID:: PMC1712440

Summary Page Browse PDF–918K

Select item 137740011.

Evidence for digenic inheritance of nonsyndromic hereditary hearing loss in a Swedish family.

J Balciuniene, N Dahl, E Borg, E Samuelsson, M J Koisti, U Pettersson, E E Jazin

Am J Hum Genet. 1998 Sep; 63(3): 786–793. doi: 10.1086/302012

PMCID:: PMC1377400

Abstract

Select item 449013212.

RWDD3 and TECTA variants not linked to paclitaxel induced peripheral neuropathy in North American trial N08C1

Amit A. Kulkarni, Ganesh Boora, Rahul Kanwar, Kathryn J. Ruddy, Michaela S. Banck, Nguyet Le-Lindqwister, Terry M. Therneau, Charles L. Loprinzi, Andreas S. Beutler

Acta Oncol. Author manuscript; available in PMC 2015 Sep 1.

Published in final edited form as: Acta Oncol. 2015 Sep; 54(8): 1227–1229. Published online 2014 Dec 31. doi: 10.3109/0284186X.2014.985388

PMCID:: PMC4490132

Article PDF–260K

Select item 171247413.

Nonsyndromic hearing impairment: unparalleled heterogeneity.

G Van Camp, P J Willems, R J Smith

Am J Hum Genet. 1997 Apr; 60(4): 758–764.

PMCID:: PMC1712474

Summary Page Browse PDF–1.2M

Select item 748705414.

A Comparative Analysis of Genetic Hearing Loss Phenotypes in European/American and Japanese Populations

W. Daniel Walls, Hideaki Moteki, Taylor R. Thomas, Shin-ya Nishio, Hidekane Yoshimura, Yoichiro Iwasa, Kathy L. Frees, Carla J. Nishimura, Hela Azaiez, Kevin T. Booth, Robert J. Marini, Diana L. Kolbe, A. Monique Weaver, Amanda M. Schaefer, Kai Wang, Terry A. Braun, Shin-ichi Usami, Peter G. Barr-Gillespie, Guy P. Richardson, Richard J. Smith, Thomas L. Casavant

Hum Genet. Author manuscript; available in PMC 2021 Oct 1.

Published in final edited form as: Hum Genet. 2020 Oct; 139(10): 1315–1323. Published online 2020 May 7. doi: 10.1007/s00439-020-02174-y

PMCID:: PMC7487054

Abstract Article PDF–1.1M

Select item 808466415.

Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families

Xueshuang Mei, Yaqi Zhou, Muhammad Amjad, Weiqiang Yang, Rufei Zhu, Muhammad Asif, Hafiz Muhammad Jafar Hussain, Tao Yang, Furhan Iqbal, Hongyi Hu

Neural Plast. 2021; 2021: 5528434. Published online 2021 Apr 22. doi: 10.1155/2021/5528434

PMCID:: PMC8084664

Abstract Article PDF–1.0M

Select item 286930416.

Deficient forward transduction and enhanced reverse transduction in the alpha tectorin C1509G human hearing loss mutation

Anping Xia, Simon S. Gao, Tao Yuan, Alexander Osborn, Andreas Bress, Markus Pfister, Stephen M. Maricich, Fred A. Pereira, John S. Oghalai

Dis Model Mech. 2010 Mar-Apr; 3(3-4): 209–223. Published online 2010 Feb 8. doi: 10.1242/dmm.004135

PMCID:: PMC2869304

Abstract Article

Select item 338112417.

Loss of Mammal-specific Tectorial Membrane Component Carcinoembryonic Antigen Cell Adhesion Molecule 16 (CEACAM16) Leads to Hearing Impairment at Low and High Frequencies

Robert Kammerer, Lukas Rüttiger, Rainer Riesenberg, Constanze Schäuble, Rosemarie Krupar, Annegret Kamp, Kishiko Sunami, Andreas Eisenried, Martin Hennenberg, Fritz Grunert, Andreas Bress, Sebastiano Battaglia, Heinrich Schrewe, Marlies Knipper, Marlon R. Schneider, Wolfgang Zimmermann

J Biol Chem. 2012 Jun 22; 287(26): 21584–21598. Published online 2012 Apr 27. doi: 10.1074/jbc.M111.320481

PMCID:: PMC3381124

Abstract Article PDF–4.0M

Select item 305400818.

Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with α-tectorin and is mutated in autosomal dominant hearing loss (DFNA4)

Jing Zheng, Katharine K. Miller, Tao Yang, Michael S. Hildebrand, A. Eliot Shearer, Adam P. DeLuca, Todd E. Scheetz, Jennifer Drummond, Steve E. Scherer, P. Kevin Legan, Richard J. Goodyear, Guy P. Richardson, Mary Ann Cheatham, Richard J. Smith, Peter Dallos

Proc Natl Acad Sci U S A. 2011 Mar 8; 108(10): 4218–4223. Published online 2011 Feb 22. doi: 10.1073/pnas.1005842108

PMCID:: PMC3054008

Abstract Article PDF–922K

Select item 436785719.

New interaction partners for Nek4.1 and Nek4.2 isoforms: from the DNA damage response to RNA splicing

Fernanda Luisa Basei, Gabriela Vaz Meirelles, Germanna Lima Righetto, Deivid Lucas dos Santos Migueleti, Juliana Helena Costa Smetana, Jörg Kobarg

Proteome Sci. 2015; 13: 11. Published online 2015 Feb 26. doi: 10.1186/s12953-015-0065-6

PMCID:: PMC4367857

Abstract Article PDF–3.1M

Select item 549522520.

Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing

Teng Fei, Yiwen Chen, Tengfei Xiao, Wei Li, Laura Cato, Peng Zhang, Maura B. Cotter, Michaela Bowden, Rosina T. Lis, Shuang G. Zhao, Qiu Wu, Felix Y. Feng, Massimo Loda, Housheng Hansen He, X. Shirley Liu, Myles Brown

Proc Natl Acad Sci U S A. 2017 Jun 27; 114(26): E5207–E5215. Published online 2017 Jun 13. doi: 10.1073/pnas.1617467114

PMCID:: PMC5495225

Abstract Article PDF–1.3M

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 23

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity