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Journal Abstract Search

231 related items for PubMed ID: 32970669

  • 1. 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.
    PLoS Genet; 2020 Sep; 16(9):e1009040. PubMed ID: 32970669
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  • 4. 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. PubMed ID: 15254021
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  • 5. Pou4f3 gene mutation promotes autophagy and apoptosis of cochlear hair cells in cisplatin-induced deafness mice.
    Xu F, Yan W, Cheng Y.
    Arch Biochem Biophys; 2020 Feb 15; 680():108224. PubMed ID: 31830441
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  • 8. 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 15; 57(4):125-8. PubMed ID: 24556497
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  • 9. 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 15; 23(22):7957-64. PubMed ID: 14585957
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  • 11. 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. PubMed ID: 9506947
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  • 12. 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 20; 24(12):6978-6987. PubMed ID: 32390314
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  • 13. 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 Jun 20; 14(5):303-7. PubMed ID: 19372648
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  • 14. In Vivo Interplay between p27Kip1, GATA3, ATOH1, and POU4F3 Converts Non-sensory Cells to Hair Cells in Adult Mice.
    Walters BJ, Coak E, Dearman J, Bailey G, Yamashita T, Kuo B, Zuo J.
    Cell Rep; 2017 Apr 11; 19(2):307-320. PubMed ID: 28402854
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  • 15. Anti-apoptotic factor z-Val-Ala-Asp-fluoromethylketone promotes the survival of cochlear hair cells in a mouse model for human deafness.
    Atar O, Avraham KB.
    Neuroscience; 2010 Jul 14; 168(3):851-7. PubMed ID: 20394804
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  • 16. 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 Jul 14; 12(5):e0177636. PubMed ID: 28545070
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  • 18. A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss.
    Zhang C, Wang M, Xiao Y, Zhang F, Zhou Y, Li J, Zheng Q, Bai X, Wang H.
    Neural Plast; 2016 Jul 14; 2016():1512831. PubMed ID: 27999687
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  • 19. Ramifications of POU4F3 variants associated with autosomal dominant hearing loss in various molecular aspects.
    Lee SY, Kim MY, Han JH, Park SS, Yun Y, Jee SC, Han JJ, Lee JH, Seok H, Choi BY.
    Sci Rep; 2023 Aug 03; 13(1):12584. PubMed ID: 37537203
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