Similar articles for PMID: 18228599

Year	Number of Results
1996	1
1998	1
1999	1
2000	3
2001	1
2002	5
2003	8
2004	6
2005	4
2006	7
2007	6
2008	13
2009	9
2010	9
2011	12
2012	13
2013	7
2014	8
2015	5
2016	6
2017	4
2018	2
2019	4
2020	4
2021	3
2022	3
2023	2
2024	0

1

Missense mutations in POU4F3 cause autosomal dominant hearing impairment DFNA15 and affect subcellular localization and DNA binding.

Collin RW, Chellappa R, Pauw RJ, Vriend G, Oostrik J, van Drunen W, Huygen PL, Admiraal R, Hoefsloot LH, Cremers FP, Xiang M, Cremers CW, Kremer H. Collin RW, et al. Hum Mutat. 2008 Apr;29(4):545-54. doi: 10.1002/humu.20693. Hum Mutat. 2008. PMID: 18228599 Free PMC article.

2

Identification of two novel mutations in POU4F3 gene associated with autosomal dominant hearing loss in Chinese families.

Bai X, Zhang F, Xiao Y, Jin Y, Zheng Q, Wang H, Xu L. Bai X, et al. J Cell Mol Med. 2020 Jun;24(12):6978-6987. doi: 10.1111/jcmm.15359. Epub 2020 May 11. J Cell Mol Med. 2020. PMID: 32390314 Free PMC article.

3

The DFNA15 deafness mutation affects POU4F3 protein stability, localization, and transcriptional activity.

Weiss S, Gottfried I, Mayrose I, Khare SL, Xiang M, Dawson SJ, Avraham KB. Weiss S, et al. Mol Cell Biol. 2003 Nov;23(22):7957-64. doi: 10.1128/MCB.23.22.7957-7964.2003. Mol Cell Biol. 2003. PMID: 14585957 Free PMC article.

4

Vestibular impairment in a Dutch DFNA15 family with an L289F mutation in POU4F3.

van Drunen FJ, Pauw RJ, Collin RW, Kremer H, Huygen PL, Cremers CW. van Drunen FJ, et al. Audiol Neurootol. 2009;14(5):303-7. doi: 10.1159/000212109. Epub 2009 Apr 15. Audiol Neurootol. 2009. PMID: 19372648

5

A Missense Mutation in POU4F3 Causes Midfrequency Hearing Loss in a Chinese ADNSHL Family.

Gao X, Xu JC, Wang WQ, Yuan YY, Bai D, Huang SS, Wang GJ, Su Y, Li J, Kang DY, Zhang MG, Lin X, Dai P. Gao X, et al. Biomed Res Int. 2018 Apr 4;2018:5370802. doi: 10.1155/2018/5370802. eCollection 2018. Biomed Res Int. 2018. PMID: 29850532 Free PMC article.

6

SNP linkage analysis and whole exome sequencing identify a novel POU4F3 mutation in autosomal dominant late-onset nonsyndromic hearing loss (DFNA15).

Kim HJ, Won HH, Park KJ, Hong SH, Ki CS, Cho SS, Venselaar H, Vriend G, Kim JW. Kim HJ, et al. PLoS One. 2013 Nov 18;8(11):e79063. doi: 10.1371/journal.pone.0079063. eCollection 2013. PLoS One. 2013. PMID: 24260153 Free PMC article. Clinical Trial.

7

A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities.

Bai D, Zhang X, Li Y, Ni J, Lan K. Bai D, et al. Biomed Res Int. 2021 Jun 21;2021:5574136. doi: 10.1155/2021/5574136. eCollection 2021. Biomed Res Int. 2021. PMID: 34250087 Free PMC article.

8

Aldh inhibitor restores auditory function in a mouse model of human deafness.

Zhu GJ, Gong S, Ma DB, Tao T, He WQ, Zhang L, Wang F, Qian XY, Zhou H, Fan C, Wang P, Chen X, Zhao W, Sun J, Chen H, Wang Y, Gao X, Zuo J, Zhu MS, Gao X, Wan G. Zhu GJ, et al. PLoS Genet. 2020 Sep 24;16(9):e1009040. doi: 10.1371/journal.pgen.1009040. eCollection 2020 Sep. PLoS Genet. 2020. PMID: 32970669 Free PMC article.

9

POU4F3 mutation screening in Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis identified novel variants associated with autosomal dominant hearing loss.

Kitano T, Miyagawa M, Nishio SY, Moteki H, Oda K, Ohyama K, Miyazaki H, Hidaka H, Nakamura KI, Murata T, Matsuoka R, Ohta Y, Nishiyama N, Kumakawa K, Furutate S, Iwasaki S, Yamada T, Ohta Y, Uehara N, Noguchi Y, Usami SI. Kitano T, et al. PLoS One. 2017 May 17;12(5):e0177636. doi: 10.1371/journal.pone.0177636. eCollection 2017. PLoS One. 2017. PMID: 28545070 Free PMC article.

10

Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3.

Pauw RJ, van Drunen FJ, Collin RW, Huygen PL, Kremer H, Cremers CW. Pauw RJ, et al. Arch Otolaryngol Head Neck Surg. 2008 Mar;134(3):294-300. doi: 10.1001/archotol.134.3.294. Arch Otolaryngol Head Neck Surg. 2008. PMID: 18347256

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