Tomoko Makishima

Summary

Affiliation: University of Texas Medical Branch
Country: USA

Publications

  1. pmc Inner ear dysfunction in caspase-3 deficient mice
    Tomoko Makishima
    Department of Otolaryngology, University of Texas Medical Branch, Galveston, Texas, USA
    BMC Neurosci 12:102. 2011
  2. doi request reprint Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss
    Brent Kelly
    University of Texas Medical Branch, Galveston, and Baylor College of Medicine, Houston, Texas, USA
    Int J Dermatol 47:443-7. 2008

Collaborators

  • Brent Kelly
  • Annabelle Lozano
  • Guillermo Altenberg

Detail Information

Publications2

  1. pmc Inner ear dysfunction in caspase-3 deficient mice
    Tomoko Makishima
    Department of Otolaryngology, University of Texas Medical Branch, Galveston, Texas, USA
    BMC Neurosci 12:102. 2011
    ..In contrast with the auditory system, details of the vestibular phenotype have not been characterized. Here we report the vestibular phenotype and inner ear anatomy in the caspase-3 deficient (Casp3(-/-)) mouse strain...
  2. doi request reprint Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss
    Brent Kelly
    University of Texas Medical Branch, Galveston, and Baylor College of Medicine, Houston, Texas, USA
    Int J Dermatol 47:443-7. 2008
    ..Keratitis-ichthyosis-deafness (KID) syndrome most commonly results from a mutation in the gap-junctional protein connexin 26 (Cx26) gene, GJB2. Most cases are sporadic and are associated with sensorineural hearing loss...