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Items: 1 to 20 of 36

1.
Genotype-Phenotype Correlations in TMPRSS3 (DFNB10/DFNB8) with Emphasis on Natural History
Eric Nisenbaum, Denise Yan, A. Eliot Shearer, Evan de Joya, Torin Thielhelm, Nicole Russell, Hinrich Staecker, Zhengyi Chen, Jeffrey R. Holt, Xuezhong Liu
Audiol Neurootol. 2023 Dec; 28(6): 407–419. Published online 2023 Jun 16. doi: 10.1159/000528766
PMCID:
PMC10857012
AbstractArticle
2.
TMPRSS3 expression is limited in spiral ganglion neurons: implication for successful cochlear implantation
Yuan-Siao Chen, Ernesto Cabrera, Brady J. Tucker, Timothy J. Shin, Jasmine V. Moawad, Douglas J. Totten, Kevin T. Booth, Rick F. Nelson
J Med Genet. Author manuscript; available in PMC 2023 Jun 7.
Published in final edited form as: J Med Genet. 2022 Dec; 59(12): 1219–1226. Published online 2022 Aug 12. doi: 10.1136/jmg-2022-108654
PMCID:
PMC10245338
AbstractArticlePDF–930K
3.
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
AbstractArticlePDF–2.2M
4.
Knockdown of TMPRSS3, a Transmembrane Serine Protease, Inhibits Proliferation, Migration, and Invasion in Human Nasopharyngeal Carcinoma Cells
Jun-Ying Wang, Xin Jin, Xiao-Feng Li
Oncol Res. 2018; 26(1): 95–101. Published online 2018 Jan 19. doi: 10.3727/096504017X14920318811695
PMCID:
PMC7844551
AbstractArticlePDF–4.4M
5.
Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss
Swee-Hee Wong, Yung-Chang Yen, Shuan-Yow Li, Jiann-Jou Yang
Int J Mol Sci. 2020 Apr; 21(7): 2382. Published online 2020 Mar 30. doi: 10.3390/ijms21072382
PMCID:
PMC7177719
AbstractArticlePDF–4.3M
6.
Overinterpretation of high throughput sequencing data in medical genetics: first evidence against TMPRSS3/GJB2 digenic inheritance of hearing loss
Monika Ołdak, Urszula Lechowicz, Agnieszka Pollak, Dominika Oziębło, Henryk Skarżyński
J Transl Med. 2019; 17: 269. Published online 2019 Aug 14. doi: 10.1186/s12967-019-2018-9
PMCID:
PMC6694500
AbstractArticlePDF–1.6M
7.
Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss
Xinlei Li, Bo Tan, Xiaoqian Wang, Xiaofei Xu, Cuicui Wang, Mingjun Zhong, Qiuling Zhao, Zhongwei Bao, Weihua Peng, Lei Zhang, Jing Cheng, Yu Lu, Peina Wu, Huijun Yuan
Mol Genet Genomic Med. 2019 Jun; 7(6): e685. Published online 2019 Apr 23. doi: 10.1002/mgg3.685
PMCID:
PMC6565588
AbstractArticlePDF–1.1M
8.
In Vivo Electrocochleography in Hybrid Cochlear Implant Users Implicates TMPRSS3 in Spiral Ganglion Function
A. Eliot Shearer, Viral D. Tejani, Carolyn J. Brown, Paul J. Abbas, Marlan R. Hansen, Bruce J. Gantz, Richard J. H. Smith
Sci Rep. 2018; 8: 14165. Published online 2018 Sep 21. doi: 10.1038/s41598-018-32630-9
PMCID:
PMC6154996
AbstractArticlePDF–3.0M
9.
Expression of trans-membrane serine protease 3 (TMPRSS3) in the human organ of Corti
Wei Liu, Hubert Löwenheim, Peter A. Santi, Rudolf Glueckert, Annelies Schrott-Fischer, Helge Rask-Andersen
Cell Tissue Res. 2018; 372(3): 445–456. Published online 2018 Feb 19. doi: 10.1007/s00441-018-2793-2
PMCID:
PMC5949142
AbstractArticlePDF–18M
10.
The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans
Ah Reum Kim, Juyong Chung, Nayoung K. D. Kim, Chung Lee, Woong-Yang Park, Doo-Yi Oh, Byung Yoon Choi
Int J Mol Sci. 2017 Nov; 18(11): 2246. Published online 2017 Oct 26. doi: 10.3390/ijms18112246
PMCID:
PMC5713216
AbstractArticlePDF–1.7M
11.
Mammalian APE1 controls miRNA processing and its interactome is linked to cancer RNA metabolism
Giulia Antoniali, Fabrizio Serra, Lisa Lirussi, Mikiei Tanaka, Chiara D’Ambrosio, Shiheng Zhang, Slobodanka Radovic, Emiliano Dalla, Yari Ciani, Andrea Scaloni, Mengxia Li, Silvano Piazza, Gianluca Tell
Nat Commun. 2017; 8: 797. Published online 2017 Oct 6. doi: 10.1038/s41467-017-00842-8
PMCID:
PMC5630600
AbstractArticlePDF–2.3M
12.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M
13.
Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population
Xue Gao, Sha-Sha Huang, Yong-Yi Yuan, Jin-Cao Xu, Ping Gu, Dan Bai, Dong-Yang Kang, Ming-Yu Han, Guo-Jian Wang, Mei-Guang Zhang, Jia Li, Pu Dai
Neural Plast. 2017; 2017: 3192090. Published online 2017 Jun 13. doi: 10.1155/2017/3192090
PMCID:
PMC5485344
AbstractArticlePDF–1.1M
14.
Iterative Sequencing and Variant Screening (ISVS) as a novel pathogenic mutations search strategy - application for TMPRSS3 mutations screen
Urszula Lechowicz, Tomasz Gambin, Agnieszka Pollak, Anna Podgorska, Piotr Stawinski, Andre Franke, Britt-Sabina Petersen, Malgorzata Firczuk, Monika Oldak, Henryk Skarzynski, Rafal Ploski
Sci Rep. 2017; 7: 2543. Published online 2017 May 31. doi: 10.1038/s41598-017-02315-w
PMCID:
PMC5451398
AbstractArticlePDF–1.3M
15.
Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment
Xue Gao, Yong-Yi Yuan, Guo-Jian Wang, Jin-Cao Xu, Yu Su, Xi Lin, Pu Dai
Biomed Res Int. 2017; 2017: 4707315. Published online 2017 Jan 29. doi: 10.1155/2017/4707315
PMCID:
PMC5303592
AbstractArticlePDF–1.9M
16.
TMPRSS3 is a novel poor prognostic factor for breast cancer
Xue Rui, Yanshu Li, Feng Jin, Feng Li
Int J Clin Exp Pathol. 2015; 8(5): 5435–5442. Published online 2015 May 1.
PMCID:
PMC4503118
AbstractArticlePDF–871K
17.
Low expression levels of hepsin and TMPRSS3 are associated with poor breast cancer survival
Mikko Pelkonen, Kaisa Luostari, Maria Tengström, Hermanni Ahonen, Bozena Berdel, Vesa Kataja, Ylermi Soini, Veli-Matti Kosma, Arto Mannermaa
BMC Cancer. 2015; 15: 431. Published online 2015 May 27. doi: 10.1186/s12885-015-1440-5
PMCID:
PMC4445813
AbstractArticlePDF–1.0M
18.
Identification of a Novel Homozygous Mutation, TMPRSS3: c.535G>A, in a Tibetan Family with Autosomal Recessive Non-Syndromic Hearing Loss
Dongyan Fan, Wei Zhu, Dejun Li, De Ji, Ping Wang
PLoS One. 2014; 9(12): e114136. Published online 2014 Dec 4. doi: 10.1371/journal.pone.0114136
PMCID:
PMC4256404
AbstractArticlePDF–921K
19.
Type II Transmembrane Serine Protease Gene Variants Associate with Breast Cancer
Kaisa Luostari, Jaana M. Hartikainen, Maria Tengström, Jorma J. Palvimo, Vesa Kataja, Arto Mannermaa, Veli-Matti Kosma
PLoS One. 2014; 9(7): e102519. Published online 2014 Jul 16. doi: 10.1371/journal.pone.0102519
PMCID:
PMC4100901
AbstractArticlePDF–451K
20.
Non-Syndromic Hearing Impairment in India: High Allelic Heterogeneity among Mutations in TMPRSS3, TMC1, USHIC, CDH23 and TMIE
Aparna Ganapathy, Nishtha Pandey, C. R. Srikumari Srisailapathy, Rajeev Jalvi, Vikas Malhotra, Mohan Venkatappa, Arunima Chatterjee, Meenakshi Sharma, Rekha Santhanam, Shelly Chadha, Arabandi Ramesh, Arun K. Agarwal, Raghunath R. Rangasayee, Anuranjan Anand
PLoS One. 2014; 9(1): e84773. Published online 2014 Jan 8. doi: 10.1371/journal.pone.0084773
PMCID:
PMC3885616
AbstractArticlePDF–2.8M

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