PubMed for id: 376173

Year	Number of Results
1997	1
1998	1
2002	4
2003	2
2004	1
2005	2
2006	2
2007	1
2008	2
2009	1
2010	1
2011	1
2014	3
2015	3
2016	2
2018	1
2019	3
2020	1
2021	1
2022	5
2023	3
2024	1

1

A novel DFNA36 mutation in TMC1 orthologous to the Beethoven (Bth) mouse associated with autosomal dominant hearing loss in a Chinese family.

Zhao Y, Wang D, Zong L, Zhao F, Guan L, Zhang P, Shi W, Lan L, Wang H, Li Q, Han B, Yang L, Jin X, Wang J, Wang J, Wang Q. Zhao Y, et al. PLoS One. 2014 May 14;9(5):e97064. doi: 10.1371/journal.pone.0097064. eCollection 2014. PLoS One. 2014. PMID: 24827932 Free PMC article.

2

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11.

Hilgert N, Alasti F, Dieltjens N, Pawlik B, Wollnik B, Uyguner O, Delmaghani S, Weil D, Petit C, Danis E, Yang T, Pandelia E, Petersen MB, Goossens D, Favero JD, Sanati MH, Smith RJ, Van Camp G. Hilgert N, et al. Clin Genet. 2008 Sep;74(3):223-32. doi: 10.1111/j.1399-0004.2008.01053.x. Epub 2008 Jul 9. Clin Genet. 2008. PMID: 18616530 Free PMC article.

3

A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1.

Kitajiri S, Makishima T, Friedman TB, Griffith AJ. Kitajiri S, et al. Clin Genet. 2007 Feb;71(2):148-52. doi: 10.1111/j.1399-0004.2007.00739.x. Clin Genet. 2007. PMID: 17250663

4

Early onset and rapid progression of dominant nonsyndromic DFNA36 hearing loss.

Makishima T, Kurima K, Brewer CC, Griffith AJ. Makishima T, et al. Otol Neurotol. 2004 Sep;25(5):714-9. doi: 10.1097/00129492-200409000-00011. Otol Neurotol. 2004. PMID: 15354000

5

Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactions.

Cho SH, Yun Y, Lee DH, Cha JH, Lee SM, Lee J, Suh MH, Lee JH, Oh SH, Park MK, Lee SY. Cho SH, et al. BMC Med Genomics. 2023 Dec 8;16(1):320. doi: 10.1186/s12920-023-01766-7. BMC Med Genomics. 2023. PMID: 38066485 Free PMC article.

6

Mutation-agnostic RNA interference with engineered replacement rescues Tmc1-related hearing loss.

Iwasa Y, Klimara MJ, Yoshimura H, Walls WD, Omichi R, West CA, Shibata SB, Ranum PT, Smith RJ. Iwasa Y, et al. Life Sci Alliance. 2022 Dec 27;6(3):e202201592. doi: 10.26508/lsa.202201592. Print 2023 Mar. Life Sci Alliance. 2022. PMID: 36574989 Free PMC article.

7

Preventing autosomal-dominant hearing loss in Bth mice with CRISPR/CasRx-based RNA editing.

Zheng Z, Li G, Cui C, Wang F, Wang X, Xu Z, Guo H, Chen Y, Tang H, Wang D, Huang M, Chen ZY, Huang X, Li H, Li GL, Hu X, Shu Y. Zheng Z, et al. Signal Transduct Target Ther. 2022 Mar 14;7(1):79. doi: 10.1038/s41392-022-00893-4. Signal Transduct Target Ther. 2022. PMID: 35283480 Free PMC article.

8

Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss.

Nishio SY, Usami SI. Nishio SY, et al. Hum Genet. 2022 Apr;141(3-4):929-937. doi: 10.1007/s00439-021-02364-2. Epub 2021 Sep 14. Hum Genet. 2022. PMID: 34523024 Free PMC article.

9

Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population.

Ramzan K, Al-Owain M, Al-Numair NS, Afzal S, Al-Ageel S, Al-Amer S, Al-Baik L, Al-Otaibi GF, Hashem A, Al-Mashharawi E, Basit S, Al-Mazroea AH, Softah A, Sogaty S, Imtiaz F. Ramzan K, et al. Am J Med Genet B Neuropsychiatr Genet. 2020 Apr;183(3):172-180. doi: 10.1002/ajmg.b.32774. Epub 2019 Dec 19. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 31854501

10

The contribution of TMC1 to adaptation of mechanoelectrical transduction channels in cochlear outer hair cells.

Goldring AC, Beurg M, Fettiplace R. Goldring AC, et al. J Physiol. 2019 Dec;597(24):5949-5961. doi: 10.1113/JP278799. Epub 2019 Nov 12. J Physiol. 2019. PMID: 31633194 Free PMC article.

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