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Select item 81650301.

Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome

Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi

Cell. Author manuscript; available in PMC 2022 May 27.

Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011

PMCID:: PMC8165030

Abstract Article PDF–2.2M

Select item 80846642.

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 74870543.

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 56133824.

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 54952255.

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

Select item 44901326.

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 43678577.

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 40162318.

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 39949669.

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 372955910.

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 338112411.

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 332666512.

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 317805913.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 305400814.

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