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Volumn 385, Issue 1, 2009, Pages 33-37

Targeted connexin26 ablation arrests postnatal development of the organ of Corti

Author keywords

Cell degeneration; Cochlear development; Connexin26 mutation; Genetic deafness; Hair cells; Mechanism of deafness; Mouse models; Spiral ganglion neuron

Indexed keywords

CONNEXIN 26;

EID: 67349148585     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.05.023     Document Type: Article
Times cited : (93)

References (19)
  • 1
    • 0242266904 scopus 로고    scopus 로고
    • Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessment of connexin composition in mammals
    • Forge A., Becker D., Casalotti S., Edwards J., Marziano N., and Nevill G. Gap junctions in the inner ear: comparison of distribution patterns in different vertebrates and assessment of connexin composition in mammals. J. Comp. Neurol. 467 (2003) 207-231
    • (2003) J. Comp. Neurol. , vol.467 , pp. 207-231
    • Forge, A.1    Becker, D.2    Casalotti, S.3    Edwards, J.4    Marziano, N.5    Nevill, G.6
  • 2
    • 0038351949 scopus 로고    scopus 로고
    • Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice
    • Ahmad S., Chen S., Sun J., and Lin X. Connexins 26 and 30 are co-assembled to form gap junctions in the cochlea of mice. Biochem. Biophys. Res. Commun. 307 (2003) 362-368
    • (2003) Biochem. Biophys. Res. Commun. , vol.307 , pp. 362-368
    • Ahmad, S.1    Chen, S.2    Sun, J.3    Lin, X.4
  • 3
    • 67349248636 scopus 로고    scopus 로고
    • Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models
    • Hoang Dinh E., Ahmad S., Chang Q., Tang W., Stong B., and Lin X. Diverse deafness mechanisms of connexin mutations revealed by studies using in vitro approaches and mouse models. Brain Res. (2009)
    • (2009) Brain Res.
    • Hoang Dinh, E.1    Ahmad, S.2    Chang, Q.3    Tang, W.4    Stong, B.5    Lin, X.6
  • 5
  • 8
    • 2342510998 scopus 로고    scopus 로고
    • Generation of Pax2-Cre mice by modification of a Pax2 bacterial artificial chromosome
    • Ohyama T., and Groves A.K. Generation of Pax2-Cre mice by modification of a Pax2 bacterial artificial chromosome. Genesis 38 (2004) 195-199
    • (2004) Genesis , vol.38 , pp. 195-199
    • Ohyama, T.1    Groves, A.K.2
  • 9
    • 0032923739 scopus 로고    scopus 로고
    • Generalized lacZ expression with the ROSA26 Cre reporter strain
    • Soriano P. Generalized lacZ expression with the ROSA26 Cre reporter strain. Nat. Genet. 21 (1999) 70-71
    • (1999) Nat. Genet. , vol.21 , pp. 70-71
    • Soriano, P.1
  • 10
    • 69449102234 scopus 로고    scopus 로고
    • Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea
    • in press
    • Y. Sun, W. Tang, Q. Chang, Y.F. Wang, Y.Y. Kong, X. Lin, Connexin30 null and conditional connexin26 null mice display distinct pattern and time course of cellular degeneration in the cochlea, J. Comp. Neurol., in press.
    • J. Comp. Neurol
    • Sun, Y.1    Tang, W.2    Chang, Q.3    Wang, Y.F.4    Kong, Y.Y.5    Lin, X.6
  • 13
    • 33846590621 scopus 로고    scopus 로고
    • Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness
    • Ahmad S., Tang W., Chang Q., Qu Y., Hibshman J., Li Y., Sohl G., Willecke K., Chen P., and Lin X. Restoration of connexin26 protein level in the cochlea completely rescues hearing in a mouse model of human connexin30-linked deafness. Proc. Natl. Acad. Sci. USA 104 (2007) 1337-1341
    • (2007) Proc. Natl. Acad. Sci. USA , vol.104 , pp. 1337-1341
    • Ahmad, S.1    Tang, W.2    Chang, Q.3    Qu, Y.4    Hibshman, J.5    Li, Y.6    Sohl, G.7    Willecke, K.8    Chen, P.9    Lin, X.10
  • 14
    • 0001239698 scopus 로고    scopus 로고
    • Development of sensory and neural structures in the mammalian cochlea
    • Rubel E.W., Popper A.N., and Fay R.R. (Eds), Springer, New York
    • Pujol R., Lavigne-Rebillard M., and Lenoir M. Development of sensory and neural structures in the mammalian cochlea. In: Rubel E.W., Popper A.N., and Fay R.R. (Eds). Development of the Auditory System (1998), Springer, New York 146-192
    • (1998) Development of the Auditory System , pp. 146-192
    • Pujol, R.1    Lavigne-Rebillard, M.2    Lenoir, M.3
  • 15
    • 0036472340 scopus 로고    scopus 로고
    • Neurodevelopmental control by thyroid hormone receptors
    • Forrest D., Reh T.A., and Rusch A. Neurodevelopmental control by thyroid hormone receptors. Curr. Opin. Neurobiol. 12 (2002) 49-56
    • (2002) Curr. Opin. Neurobiol. , vol.12 , pp. 49-56
    • Forrest, D.1    Reh, T.A.2    Rusch, A.3
  • 17
    • 27244452111 scopus 로고    scopus 로고
    • Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions
    • Zhang Y., Tang W., Ahmad S., Sipp J.A., Chen P., and Lin X. Gap junction-mediated intercellular biochemical coupling in cochlear supporting cells is required for normal cochlear functions. Proc. Natl. Acad. Sci. USA 102 (2005) 15201-15206
    • (2005) Proc. Natl. Acad. Sci. USA , vol.102 , pp. 15201-15206
    • Zhang, Y.1    Tang, W.2    Ahmad, S.3    Sipp, J.A.4    Chen, P.5    Lin, X.6
  • 18
    • 12344304163 scopus 로고    scopus 로고
    • Impaired permeability to Ins(1, 4, 5)P3 in a mutant connexin underlies recessive hereditary deafness
    • Beltramello M., Piazza V., Bukauskas F.F., Pozzan T., and Mammano F. Impaired permeability to Ins(1, 4, 5)P3 in a mutant connexin underlies recessive hereditary deafness. Nat. Cell Biol. 7 (2005) 63-69
    • (2005) Nat. Cell Biol. , vol.7 , pp. 63-69
    • Beltramello, M.1    Piazza, V.2    Bukauskas, F.F.3    Pozzan, T.4    Mammano, F.5
  • 19
    • 58149354499 scopus 로고    scopus 로고
    • Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice
    • Chang Q., Tang W., Ahmad S., Zhou B., and Lin X. Gap junction mediated intercellular metabolite transfer in the cochlea is compromised in connexin30 null mice. PLoS ONE 3 (2008) e4088
    • (2008) PLoS ONE , vol.3
    • Chang, Q.1    Tang, W.2    Ahmad, S.3    Zhou, B.4    Lin, X.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.