39
Views
3
CrossRef citations to date
0
Altmetric
ORIGINAL ARTICLE

The inner ear phenotype of Volchok (Vlk): An ENU-induced mouse model for CHARGE syndrome

, , , , &
Pages 110-119 | Published online: 01 Jun 2010

References

  • Highstein SM. Anatomy and Physiology of the Central and Peripheral Vestibular System: Overview. Fay RR, Popper AN. The Vestibular System. New York: Springer-Verlag; 2004. 1–10.
  • Bear MF, Connors BW, Paradiso MA. The Auditory and Vestibular Systems. Lupash E, Connolly E, Dilernia B, Williams PC. Neuroscience: Exploring the Brain. Baltimore: Lippincott Williams & Wilkins; 2006. 343–86.
  • Petit C, Levilliers J, Hardelin JP. Molecular genetics of hearing loss. Annu Rev Genet. 2001;35:589–646.
  • Dror AA, Avraham KB. Hearing loss: mechanisms revealed by genetics and cell biology. Annu Rev Genet. 2009;43:411–37.
  • Hrabe de Angelis MH, Flaswinkel H, Fuchs H, Rathkolb B, Soewarto D, Marschall S, . Genome-wide, large-scale production of mutant mice by ENU mutagenesis. Nat Genet. 2000;25:444–7.
  • Wall C 3rd, Merfeld DM, Rauch SD, Black FO. Vestibular prostheses: the engineering and biomedical issues. J Vestib Res. 2002;12:95–113.
  • Staecker H, Praetorius M, Baker K, Brough DE. Vestibular hair cell regeneration and restoration of balance function induced by math1 gene transfer. Otol Neurotol. 2007;28: 223–31.
  • Gananca CF, Caovilla HH, Gazzola JM, Gananca MM, Gananca FF. Epley's manoeuvre in benign paroxysmal positional vertigo associated with Ménière's disease. Rev Bras Otorrinolaringol (Engl Ed). 2007;73:506–12.
  • Vissers LE, van Ravenswaaij CM, Admiraal R, Hurst JA, de Vries BB, Janssen IM, . Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Nat Genet. 2004;36:955–7.
  • Bosman EA, Penn AC, Ambrose JC, Kettleborough R, Stemple DL, Steel KP. Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. Hum Mol Genet. 2005;14:3463–76.
  • Abadie V, Wiener-Vacher S, Morisseau-Durand MP, Poree C, Amiel J, Amanou L, . Vestibular anomalies in CHARGE syndrome: investigations on and consequences for postural development. Eur J Pediatr. 2000;159:569–74.
  • Delahaye A, Sznajer Y, Lyonnet S, Elmaleh-Berges M, Delpierre I, Audollent S, . Familial CHARGE syndrome because of CHD7 mutation: clinical intra- and inter-familial variability. Clin Genet. 2007;72:112–21.
  • Adams ME, Hurd EA, Beyer LA, Swiderski DL, Raphael Y, Martin DM. Defects in vestibular sensory epithelia and innervation in mice with loss of Chd7 function: implications for human CHARGE syndrome. J Comp Neurol. 2007;504:519–32.
  • Green EC, Gkoutos GV, Lad HV, Blake A, Weekes J, Hancock JM. EMPReSS: European mouse phenotyping resource for standardized screens. Bioinformatics. 2005;21:2930–1.
  • Self T, Sobe T, Copeland NG, Jenkins NA, Avraham KB, Steel KP. Role of myosin VI in the differentiation of cochlear hair cells. Dev Biol. 1999;214:331–41.
  • Bissonnette JP, Fekete DM. Standard atlas of the gross anatomy of the developing inner ear of the chicken. J Comp Neurol. 1996;368:620–30.
  • Kiernan AE, Erven A, Voegeling S, Peters J, Nolan P, Hunter J, . ENU mutagenesis reveals a highly mutable locus on mouse chromosome 4 that affects ear morphogenesis. Mamm Genome. 2002;13:142–8.
  • Alavizadeh A, Kiernan AE, Nolan P, Lo C, Steel KP, Bucan M. The Wheels mutation in the mouse causes vascular, hindbrain, and inner ear defects. Dev Biol. 2001;234:244–60.
  • Avni R, Elkan T, Dror AA, Shefer S, Eilam D, Avraham KB, . Mice with vestibular deficiency display hyperactivity, disorientation, and signs of anxiety. Behav Brain Res. 2009;202:210–7.
  • Smith PF, Darlington CL, Zheng Y. Move it or lose it: is stimulation of the vestibular system necessary for normal spatial memory? Hippocampus. 2010;20:36–43.
  • Kandler K, Clause A, Noh J. Tonotopic reorganization of developing auditory brainstem circuits. Nat Neurosci. 2009;12:711–7.
  • Srinivasan S, Dorighi KM, Tamkun JW. Drosophila Kismet regulates histone H3 lysine 27 methylation and early elongation by RNA polymerase II. PLoS Genet. 2008;4:1000217.
  • Hall JA, Georgel PT. CHD proteins: a diverse family with strong ties. Biochem Cell Biol. 2007;85:463–76.
  • Schnetz MP, Bartels CF, Shastri K, Balasubramanian D, Zentner GE, Balaji R, . Genomic distribution of CHD7 on chromatin tracks H3K4 methylation patterns. Genome Res. 2009;19:590–601.
  • Takada I, Mihara M, Suzawa M, Ohtake F, Kobayashi S, Igarashi M, . A histone lysine methyltransferase activated by non-canonical Wnt signalling suppresses PPAR-gamma transactivation. Nat Cell Biol. 2007;9:1273–85.
  • Qian D, Jones C, Rzadzinska A, Mark S, Zhang X, Steel KP, . Wnt5a functions in planar cell polarity regulation in mice. Dev Biol. 2007;306:121–33.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.