205 related articles for article (PubMed ID: 25372459)
21. Generation of mature and functional hair cells by co-expression of Gfi1, Pou4f3, and Atoh1 in the postnatal mouse cochlea.
Chen Y; Gu Y; Li Y; Li GL; Chai R; Li W; Li H
Cell Rep; 2021 Apr; 35(3):109016. PubMed ID: 33882317
[TBL] [Abstract][Full Text] [Related]
22. A Novel Nonsense Mutation of
Zhang C; Wang M; Xiao Y; Zhang F; Zhou Y; Li J; Zheng Q; Bai X; Wang H
Neural Plast; 2016; 2016():1512831. PubMed ID: 27999687
[No Abstract] [Full Text] [Related]
23. The Promoter and Multiple Enhancers of the pou4f3 Gene Regulate Expression in Inner Ear Hair Cells.
Masuda M; Li Y; Pak K; Chavez E; Mullen L; Ryan AF
Mol Neurobiol; 2017 Sep; 54(7):5414-5426. PubMed ID: 27592349
[TBL] [Abstract][Full Text] [Related]
24. The Effect of the MicroRNA-183 Family on Hair Cell-Specific Markers of Human Bone Marrow-Derived Mesenchymal Stem Cells.
Mahmoudian-Sani MR; Jami MS; Mahdavinezhad A; Amini R; Farnoosh G; Saidijam M
Audiol Neurootol; 2018; 23(4):208-215. PubMed ID: 30380528
[TBL] [Abstract][Full Text] [Related]
25. In Vivo Interplay between p27
Walters BJ; Coak E; Dearman J; Bailey G; Yamashita T; Kuo B; Zuo J
Cell Rep; 2017 Apr; 19(2):307-320. PubMed ID: 28402854
[TBL] [Abstract][Full Text] [Related]
26. 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
J Cell Mol Med; 2020 Jun; 24(12):6978-6987. PubMed ID: 32390314
[TBL] [Abstract][Full Text] [Related]
27. Norrie disease protein is essential for cochlear hair cell maturation.
Hayashi Y; Chiang H; Tian C; Indzhykulian AA; Edge ASB
Proc Natl Acad Sci U S A; 2021 Sep; 118(39):. PubMed ID: 34544869
[TBL] [Abstract][Full Text] [Related]
28. Hair cell overexpression of Islet1 reduces age-related and noise-induced hearing loss.
Huang M; Kantardzhieva A; Scheffer D; Liberman MC; Chen ZY
J Neurosci; 2013 Sep; 33(38):15086-94. PubMed ID: 24048839
[TBL] [Abstract][Full Text] [Related]
29. 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
PLoS One; 2017; 12(5):e0177636. PubMed ID: 28545070
[TBL] [Abstract][Full Text] [Related]
30. Mutation in the Hair Cell Specific Gene
He L; Pang X; Chen P; Wu H; Yang T
Neural Plast; 2016; 2016():9890827. PubMed ID: 28053790
[TBL] [Abstract][Full Text] [Related]
31. BDNF gene therapy induces auditory nerve survival and fiber sprouting in deaf Pou4f3 mutant mice.
Fukui H; Wong HT; Beyer LA; Case BG; Swiderski DL; Di Polo A; Ryan AF; Raphael Y
Sci Rep; 2012; 2():838. PubMed ID: 23150788
[TBL] [Abstract][Full Text] [Related]
32. 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; 400(1-2):89-97. PubMed ID: 17611044
[TBL] [Abstract][Full Text] [Related]
33. 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
PLoS One; 2013; 8(11):e79063. PubMed ID: 24260153
[TBL] [Abstract][Full Text] [Related]
34. 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
Audiol Neurootol; 2009; 14(5):303-7. PubMed ID: 19372648
[TBL] [Abstract][Full Text] [Related]
35. 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. PubMed ID: 24556497
[TBL] [Abstract][Full Text] [Related]
36. Transcription factor induced conversion of human fibroblasts towards the hair cell lineage.
Duran Alonso MB; Lopez Hernandez I; de la Fuente MA; Garcia-Sancho J; Giraldez F; Schimmang T
PLoS One; 2018; 13(7):e0200210. PubMed ID: 29979748
[TBL] [Abstract][Full Text] [Related]
37. Sonic hedgehog (SHH) promotes the differentiation of mouse cochlear neural progenitors via the Math1-Brn3.1 signaling pathway in vitro.
Hu X; Huang J; Feng L; Fukudome S; Hamajima Y; Lin J
J Neurosci Res; 2010 Apr; 88(5):927-35. PubMed ID: 19908278
[TBL] [Abstract][Full Text] [Related]
38. A Missense Mutation in
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
Biomed Res Int; 2018; 2018():5370802. PubMed ID: 29850532
[TBL] [Abstract][Full Text] [Related]
39. Deciphering the genetic interactions between Pou4f3, Gfi1, and Rbm24 in maintaining mouse cochlear hair cell survival.
Wang G; Gu Y; Liu Z
Elife; 2024 Mar; 12():. PubMed ID: 38483314
[TBL] [Abstract][Full Text] [Related]
40. Brn-3c (POU4F3) regulates BDNF and NT-3 promoter activity.
Clough RL; Sud R; Davis-Silberman N; Hertzano R; Avraham KB; Holley M; Dawson SJ
Biochem Biophys Res Commun; 2004 Nov; 324(1):372-81. PubMed ID: 15465029
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]