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Items: 1 to 20 of 97

1.

Inhibition of Myo6 gene expression by co‑expression of a mutant of transcription factor POU4F3 (BRN‑3C) in hair cells.

Ma DB, Chen J, Xia Y, Zhu GJ, Ma XF, Zhou H, Gu YJ, Yu CJ, Zhu MS, Qian XY, Gao X.

Mol Med Rep. 2014 Apr;9(4):1185-90. doi: 10.3892/mmr.2014.1953. Epub 2014 Feb 17.

PMID:
24535414
2.

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.

Hum Mol Genet. 2004 Sep 15;13(18):2143-53. Epub 2004 Jul 14.

PMID:
15254021
3.

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.

Hum Mutat. 2008 Apr;29(4):545-54. doi: 10.1002/humu.20693.

4.

Regulation of the orphan nuclear receptor Nr2f2 by the DFNA15 deafness gene Pou4f3.

Tornari C, Towers ER, Gale JE, Dawson SJ.

PLoS One. 2014 Nov 5;9(11):e112247. doi: 10.1371/journal.pone.0112247. eCollection 2014.

5.

A splice-site mutation and overexpression of MYO6 cause a similar phenotype in two families with autosomal dominant hearing loss.

Hilgert N, Topsakal V, van Dinther J, Offeciers E, Van de Heyning P, Van Camp G.

Eur J Hum Genet. 2008 May;16(5):593-602. doi: 10.1038/sj.ejhg.5202000. Epub 2008 Jan 23.

6.
7.

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.

Mol Cell Biol. 2003 Nov;23(22):7957-64.

8.

Regulation of POU4F3 gene expression in hair cells by 5' DNA in mice.

Masuda M, Dulon D, Pak K, Mullen LM, Li Y, Erkman L, Ryan AF.

Neuroscience. 2011 Dec 1;197:48-64. doi: 10.1016/j.neuroscience.2011.09.033. Epub 2011 Sep 19.

9.

TFE2 and GATA3 enhance induction of POU4F3 and myosin VIIa positive cells in nonsensory cochlear epithelium by ATOH1.

Masuda M, Pak K, Chavez E, Ryan AF.

Dev Biol. 2012 Dec 1;372(1):68-80. doi: 10.1016/j.ydbio.2012.09.002. Epub 2012 Sep 15.

10.

Molecular modelling insights into DFNA15 mediated enhancement of POU4F3 stability.

Frenz CM, Lefebvre PP.

Int J Comput Biol Drug Des. 2008;1(3):295-301.

PMID:
20054994
11.

Lhx3, a LIM domain transcription factor, is regulated by Pou4f3 in the auditory but not in the vestibular system.

Hertzano R, Dror AA, Montcouquiol M, Ahmed ZM, Ellsworth B, Camper S, Friedman TB, Kelley MW, Avraham KB.

Eur J Neurosci. 2007 Feb;25(4):999-1005.

12.

Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.

Williams LH, Miller KA, Dahl HH, Manji SS.

Hear Res. 2013 May;299:53-62. doi: 10.1016/j.heares.2013.02.006. Epub 2013 Feb 26.

PMID:
23485424
13.

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.

Science. 1998 Mar 20;279(5358):1950-4.

14.
15.

A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss.

Lee HK, Park HJ, Lee KY, Park R, Kim UK.

Biochem Biophys Res Commun. 2010 Jun 4;396(3):626-30. doi: 10.1016/j.bbrc.2010.04.132. Epub 2010 Apr 29. Erratum in: Biochem Biophys Res Commun. 2010 Aug 6;398(4):790.

PMID:
20434433
16.

Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse.

Mochizuki E, Okumura K, Ishikawa M, Yoshimoto S, Yamaguchi J, Seki Y, Wada K, Yokohama M, Ushiki T, Tokano H, Ishii R, Shitara H, Taya C, Kitamura K, Yonekawa H, Kikkawa Y.

Exp Anim. 2010;59(1):57-71.

17.

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.

Eur J Med Genet. 2014 Mar;57(4):125-8. doi: 10.1016/j.ejmg.2014.02.006. Epub 2014 Feb 18.

PMID:
24556497
18.

In vivo analysis of the myosin heavy chain IIB promoter region.

Swoap SJ.

Am J Physiol. 1998 Mar;274(3 Pt 1):C681-7.

19.

Identification and functional analysis of common sequence variants in the DFNA15 gene, Brn-3c.

Nolan LS, Jagutpal SS, Cadge BA, Woo P, Dawson SJ.

Gene. 2007 Oct 1;400(1-2):89-97. Epub 2007 Jun 12.

PMID:
17611044
20.

Atoh1 directs hair cell differentiation and survival in the late embryonic mouse inner ear.

Chonko KT, Jahan I, Stone J, Wright MC, Fujiyama T, Hoshino M, Fritzsch B, Maricich SM.

Dev Biol. 2013 Sep 15;381(2):401-10. doi: 10.1016/j.ydbio.2013.06.022. Epub 2013 Jun 21.

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