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Journal Abstract Search

304 related items for PubMed ID: 23614009

  • 1. Continued expression of GATA3 is necessary for cochlear neurosensory development.
    Duncan JS, Fritzsch B.
    PLoS One; 2013; 8(4):e62046. PubMed ID: 23614009
    [Abstract] [Full Text] [Related]

  • 2. Conditional deletion of Atoh1 using Pax2-Cre results in viable mice without differentiated cochlear hair cells that have lost most of the organ of Corti.
    Pan N, Jahan I, Kersigo J, Kopecky B, Santi P, Johnson S, Schmitz H, Fritzsch B.
    Hear Res; 2011 May; 275(1-2):66-80. PubMed ID: 21146598
    [Abstract] [Full Text] [Related]

  • 3. GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea.
    Luo XJ, Deng M, Xie X, Huang L, Wang H, Jiang L, Liang G, Hu F, Tieu R, Chen R, Gan L.
    Hum Mol Genet; 2013 Sep 15; 22(18):3609-23. PubMed ID: 23666531
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  • 4. Development in the Mammalian Auditory System Depends on Transcription Factors.
    Elliott KL, Pavlínková G, Chizhikov VV, Yamoah EN, Fritzsch B.
    Int J Mol Sci; 2021 Apr 18; 22(8):. PubMed ID: 33919542
    [Abstract] [Full Text] [Related]

  • 5. Limited inner ear morphogenesis and neurosensory development are possible in the absence of GATA3.
    Duncan JS, Lim KC, Engel JD, Fritzsch B.
    Int J Dev Biol; 2011 Apr 18; 55(3):297-303. PubMed ID: 21553382
    [Abstract] [Full Text] [Related]

  • 6. Defects in sensory organ morphogenesis and generation of cochlear hair cells in Gata3-deficient mouse embryos.
    Haugas M, Lilleväli K, Salminen M.
    Hear Res; 2012 Jan 18; 283(1-2):151-61. PubMed ID: 22094003
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  • 7. Gata3 is required in late proneurosensory development for proper sensory cell formation and organization.
    Blinkiewicz PV, Long MR, Stoner ZA, Ketchum EM, Sheltz-Kempf SN, Duncan JS.
    Sci Rep; 2023 Aug 03; 13(1):12573. PubMed ID: 37537240
    [Abstract] [Full Text] [Related]

  • 8. Gata3 is required for the functional maturation of inner hair cells and their innervation in the mouse cochlea.
    Bardhan T, Jeng JY, Waldmann M, Ceriani F, Johnson SL, Olt J, Rüttiger L, Marcotti W, Holley MC.
    J Physiol; 2019 Jul 03; 597(13):3389-3406. PubMed ID: 31069810
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  • 14. Incomplete and delayed Sox2 deletion defines residual ear neurosensory development and maintenance.
    Dvorakova M, Jahan I, Macova I, Chumak T, Bohuslavova R, Syka J, Fritzsch B, Pavlinkova G.
    Sci Rep; 2016 Dec 05; 6():38253. PubMed ID: 27917898
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  • 15. Neurosensory development and cell fate determination in the human cochlea.
    Locher H, Frijns JH, van Iperen L, de Groot JC, Huisman MA, Chuva de Sousa Lopes SM.
    Neural Dev; 2013 Oct 16; 8():20. PubMed ID: 24131517
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  • 16. Chromatin remodeler CHD7 is critical for cochlear morphogenesis and neurosensory patterning.
    Balendran V, Skidmore JM, Ritter KE, Gao J, Cimerman J, Beyer LA, Hurd EA, Raphael Y, Martin DM.
    Dev Biol; 2021 Sep 16; 477():11-21. PubMed ID: 34004180
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  • 18. Neurod1 suppresses hair cell differentiation in ear ganglia and regulates hair cell subtype development in the cochlea.
    Jahan I, Pan N, Kersigo J, Fritzsch B.
    PLoS One; 2010 Jul 22; 5(7):e11661. PubMed ID: 20661473
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  • 20. Expression of Neurog1 instead of Atoh1 can partially rescue organ of Corti cell survival.
    Jahan I, Pan N, Kersigo J, Calisto LE, Morris KA, Kopecky B, Duncan JS, Beisel KW, Fritzsch B.
    PLoS One; 2012 Jul 22; 7(1):e30853. PubMed ID: 22292060
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