PubMed (RefSeq) for id: 1812636094

Year	Number of Results
1993	1
1997	2
1998	3
1999	4
2001	1
2002	1
2003	1
2004	1
2006	2
2007	4
2008	4
2009	2
2010	3
2011	4
2012	5
2013	2
2014	5
2015	3
2016	3
2017	3
2019	2
2020	1
2021	2
2022	1
2023	1
2024	0

1

Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing loss.

Chen R, Diaz-Miranda MA, Aref-Eshghi E, Hartman TR, Griffith C, Morrison JL, Wheeler PG, Torti E, Richard G, Kenna M, Dechene ET, Spinner NB, Bai R, Conlin LK, Krantz ID, Amr SS, Luo M. Chen R, et al. Hum Mutat. 2022 Dec;43(12):1837-1843. doi: 10.1002/humu.24443. Epub 2022 Aug 2. Hum Mutat. 2022. PMID: 35870179

2

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

Mei X, Zhou Y, Amjad M, Yang W, Zhu R, Asif M, Hussain HMJ, Yang T, Iqbal F, Hu H. Mei X, et al. Neural Plast. 2021 Apr 22;2021:5528434. doi: 10.1155/2021/5528434. eCollection 2021. Neural Plast. 2021. PMID: 33976695 Free PMC article.

3

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, Szpyt J, Gassaway BM, Panov A, Parzen H, Fu S, Golbazi A, Maenpaa E, Stricker K, Guha Thakurta S, Zhang T, Rad R, Pan J, Nusinow DP, Paulo JA, Schweppe DK, Vaites LP, Harper JW, Gygi SP. Huttlin EL, et al. Cell. 2021 May 27;184(11):3022-3040.e28. doi: 10.1016/j.cell.2021.04.011. Epub 2021 May 6. Cell. 2021. PMID: 33961781 Free PMC article.

4

A comparative analysis of genetic hearing loss phenotypes in European/American and Japanese populations.

Walls WD, Moteki H, Thomas TR, Nishio SY, Yoshimura H, Iwasa Y, Frees KL, Nishimura CJ, Azaiez H, Booth KT, Marini RJ, Kolbe DL, Weaver AM, Schaefer AM, Wang K, Braun TA, Usami SI, Barr-Gillespie PG, Richardson GP, Smith RJ, Casavant TL. Walls WD, et al. Hum Genet. 2020 Oct;139(10):1315-1323. doi: 10.1007/s00439-020-02174-y. Epub 2020 May 7. Hum Genet. 2020. PMID: 32382995 Free PMC article.

5

Inflammation-dependent overexpression of c-Myc enhances CRL4^DCAF4 E3 ligase activity and promotes ubiquitination of ST7 in colitis-associated cancer.

Liu H, Lu W, He H, Wu J, Zhang C, Gong H, Yang C. Liu H, et al. J Pathol. 2019 Aug;248(4):464-475. doi: 10.1002/path.5273. Epub 2019 Apr 22. J Pathol. 2019. PMID: 30945288

6

[Diagnosis and reproductive guidance for a couple carrying a novel c.1893C>T mutation of the TECTA gene].

Zhou C, Li S, Song Q, Liu X, Miao Z. Zhou C, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Feb 10;36(2):147-150. doi: 10.3760/cma.j.issn.1003-9406.2019.02.013. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 30703234 Chinese.

7

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

Yamamoto N, Mutai H, Namba K, Morita N, Masuda S, Nishi Y, Nakano A, Masuda S, Fujioka M, Kaga K, Ogawa K, Matsunaga T. Yamamoto N, et al. Orphanet J Rare Dis. 2017 Sep 25;12(1):157. doi: 10.1186/s13023-017-0708-z. Orphanet J Rare Dis. 2017. PMID: 28946916 Free PMC article.

8

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

Fei T, Chen Y, Xiao T, Li W, Cato L, Zhang P, Cotter MB, Bowden M, Lis RT, Zhao SG, Wu Q, Feng FY, Loda M, He HH, Liu XS, Brown M. Fei T, et al. Proc Natl Acad Sci U S A. 2017 Jun 27;114(26):E5207-E5215. doi: 10.1073/pnas.1617467114. Epub 2017 Jun 13. Proc Natl Acad Sci U S A. 2017. PMID: 28611215 Free PMC article.

9

A novel TECTA mutation causes ARNSHL.

Asgharzade S, Tabatabaiefar MA, Modarressi MH, Ghahremani MH, Reiisi S, Tahmasebi P, Abdollahnejad F, Chaleshtori MH. Asgharzade S, et al. Int J Pediatr Otorhinolaryngol. 2017 Jan;92:88-93. doi: 10.1016/j.ijporl.2016.11.010. Epub 2016 Nov 15. Int J Pediatr Otorhinolaryngol. 2017. PMID: 28012541 Free article.

10

A novel biallelic splice site mutation of TECTA causes moderate to severe hearing impairment in an Algerian family.

Behlouli A, Bonnet C, Abdi S, Hasbellaoui M, Boudjenah F, Hardelin JP, Louha M, Makrelouf M, Ammar-Khodja F, Zenati A, Petit C. Behlouli A, et al. Int J Pediatr Otorhinolaryngol. 2016 Aug;87:28-33. doi: 10.1016/j.ijporl.2016.04.040. Epub 2016 May 20. Int J Pediatr Otorhinolaryngol. 2016. PMID: 27368438

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