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Journal Abstract Search

103 related items for PubMed ID: 10587581

  • 1.
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  • 2. Targeted mutagenesis of the POU-domain gene Brn4/Pou3f4 causes developmental defects in the inner ear.
    Phippard D, Lu L, Lee D, Saunders JC, Crenshaw EB.
    J Neurosci; 1999 Jul 15; 19(14):5980-9. PubMed ID: 10407036
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  • 3. Mutation of the POU-domain gene Brn4/Pou3f4 affects middle-ear sound conduction in the mouse.
    Samadi DS, Saunders JC, Crenshaw EB.
    Hear Res; 2005 Jan 15; 199(1-2):11-21. PubMed ID: 15574296
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  • 4. Changes in the subcellular localization of the Brn4 gene product precede mesenchymal remodeling of the otic capsule.
    Phippard D, Heydemann A, Lechner M, Lu L, Lee D, Kyin T, Crenshaw EB.
    Hear Res; 1998 Jun 15; 120(1-2):77-85. PubMed ID: 9667433
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  • 5. The role of Brn4/Pou3f4 and Pax6 in forming the pancreatic glucagon cell identity.
    Heller RS, Stoffers DA, Liu A, Schedl A, Crenshaw EB, Madsen OD, Serup P.
    Dev Biol; 2004 Apr 01; 268(1):123-34. PubMed ID: 15031110
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  • 7. Otic mesenchyme expression of Cre recombinase directed by the inner ear enhancer of the Brn4/Pou3f4 gene.
    Ahn KJ, Passero F, Crenshaw EB.
    Genesis; 2009 Mar 01; 47(3):137-41. PubMed ID: 19217071
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  • 9. Multiple enhancers located in a 1-Mb region upstream of POU3F4 promote expression during inner ear development and may be required for hearing.
    Naranjo S, Voesenek K, de la Calle-Mustienes E, Robert-Moreno A, Kokotas H, Grigoriadou M, Economides J, Van Camp G, Hilgert N, Moreno F, Alsina B, Petersen MB, Kremer H, Gómez-Skarmeta JL.
    Hum Genet; 2010 Oct 01; 128(4):411-9. PubMed ID: 20668882
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  • 10. Clinical and molecular characterizations of novel POU3F4 mutations reveal that DFN3 is due to null function of POU3F4 protein.
    Lee HK, Song MH, Kang M, Lee JT, Kong KA, Choi SJ, Lee KY, Venselaar H, Vriend G, Lee WS, Park HJ, Kwon TK, Bok J, Kim UK.
    Physiol Genomics; 2009 Nov 06; 39(3):195-201. PubMed ID: 19671658
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  • 12. A duplication/paracentric inversion associated with familial X-linked deafness (DFN3) suggests the presence of a regulatory element more than 400 kb upstream of the POU3F4 gene.
    de Kok YJ, Merkx GF, van der Maarel SM, Huber I, Malcolm S, Ropers HH, Cremers FP.
    Hum Mol Genet; 1995 Nov 06; 4(11):2145-50. PubMed ID: 8589693
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  • 15. Molecular analysis of the POU3F4 gene in patients with clinical and radiographic evidence of X-linked mixed deafness with perilymphatic gusher.
    Friedman RA, Bykhovskaya Y, Tu G, Talbot JM, Wilson DF, Parnes LS, Fischel-Ghodsian N.
    Ann Otol Rhinol Laryngol; 1997 Apr 06; 106(4):320-5. PubMed ID: 9109724
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  • 17. Research progress of the transcription factor Brn4 (Review).
    Wu Y, Zhang X, Wang J, Jin G, Zhang X.
    Mol Med Rep; 2021 Mar 06; 23(3):. PubMed ID: 33398372
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  • 18. Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4.
    de Kok YJ, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, Pembrey ME, Ropers HH, Cremers FP.
    Science; 1995 Feb 03; 267(5198):685-8. PubMed ID: 7839145
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  • 19. HRCT and MRI findings in X-linked non-syndromic deafness patients with a POU3F4 mutation.
    Gong WX, Gong RZ, Zhao B.
    Int J Pediatr Otorhinolaryngol; 2014 Oct 03; 78(10):1756-62. PubMed ID: 25175280
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  • 20. The molecular basis of X-linked deafness type 3 (DFN3) in two sporadic cases: identification of a somatic mosaicism for a POU3F4 missense mutation.
    de Kok YJ, Cremers CW, Ropers HH, Cremers FP.
    Hum Mutat; 1997 Oct 03; 10(3):207-11. PubMed ID: 9298820
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