Similar articles for PMID: 9506947

Year	Number of Results
1992	1
1994	1
1995	2
1996	3
1997	3
1998	5
1999	4
2000	10
2001	3
2002	6
2003	4
2004	5
2006	2
2007	4
2008	7
2009	3
2010	3
2011	3
2012	3
2013	3
2014	4
2015	1
2016	5
2017	5
2018	5
2019	3
2020	5
2021	3
2023	1
2024	0

1

Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, Blumenfeld A, Frydman M, Friedman TB, King MC, Avraham KB. Vahava O, et al. Science. 1998 Mar 20;279(5358):1950-4. doi: 10.1126/science.279.5358.1950. Science. 1998. PMID: 9506947

2

Progress in progressive hearing loss.

Steel KP. Steel KP. Science. 1998 Mar 20;279(5358):1870-1. doi: 10.1126/science.279.5358.1870. Science. 1998. PMID: 9537904 No abstract available.

3

DFNA15.

Avraham KB. Avraham KB. Adv Otorhinolaryngol. 2000;56:107-15. doi: 10.1159/000059091. Adv Otorhinolaryngol. 2000. PMID: 10868222 No abstract available.

4

Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss.

Freitas ÉL, Oiticica J, Silva AG, Bittar RS, Rosenberg C, Mingroni-Netto RC. Freitas ÉL, et al. Eur J Med Genet. 2014 Mar;57(4):125-8. doi: 10.1016/j.ejmg.2014.02.006. Epub 2014 Feb 18. Eur J Med Genet. 2014. PMID: 24556497 Free article.

5

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.

6

Clinical characterization of genetic hearing loss caused by a mutation in the POU4F3 transcription factor.

Frydman M, Vreugde S, Nageris BI, Weiss S, Vahava O, Avraham KB. Frydman M, et al. Arch Otolaryngol Head Neck Surg. 2000 May;126(5):633-7. doi: 10.1001/archotol.126.5.633. Arch Otolaryngol Head Neck Surg. 2000. PMID: 10807331

7

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.

8

Transcription profiling of inner ears from Pou4f3(ddl/ddl) identifies Gfi1 as a target of the Pou4f3 deafness gene.

Hertzano R, Montcouquiol M, Rashi-Elkeles S, Elkon R, Yücel R, Frankel WN, Rechavi G, Möröy T, Friedman TB, Kelley MW, Avraham KB. Hertzano R, et al. Hum Mol Genet. 2004 Sep 15;13(18):2143-53. doi: 10.1093/hmg/ddh218. Epub 2004 Jul 14. Hum Mol Genet. 2004. PMID: 15254021

9

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.

10

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.

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