Hair cells in the inner ear of the pirouette and shaker 2 mutant mice

Journal of Neurocytology

Volumn 29, Issue 4, 2000, Pages 227-240

  Beyer, L A ^a   Odeh, H ^a   Probst, F J ^b   Lambert, E H ^a   Dolan, D F ^a   Camper, S A ^b   Kohrman, D C ^a   Raphael, Y ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

^b UNIVERSITY OF MICHIGAN SCHOOL OF PUBLIC HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL TISSUE; ARTICLE; BASEMENT MEMBRANE; CELL DIFFERENTIATION; CONTROLLED STUDY; EVOKED BRAIN STEM AUDITORY RESPONSE; HAIR CELL; HEARING IMPAIRMENT; INNER EAR; MOUSE; NONHUMAN; PRIORITY JOURNAL; STEREOCILIUM;

ANIMALIA;

EID: 0033636642     PISSN: 03004864     EISSN: None     Source Type: Journal    
DOI: 10.1023/a:1026515619443     Document Type: Article

References (16)

1. Vestibular hair cell pathology in the Shaker 2 mouse
2. Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice
3. Inner ear pathology in the deafness mutant mouse
4. Morphologic changes in vestibular hair cells in a strain of the waltzing guinea pig
5. Unconventional myosins in inner-ear sensory epithelia
6. Developmental morphology of the mouse inner ear. A scanning electron microscopic observation
7. Correction of deafness in shaker 2 mice by an unconventional myosin in a BAC transgene
8. The sensory epithelium and its innervation in the mole rat cochlea
9. The embryonic and postnatal development of the inner ear of the mouse
10. Structure of the mammalian cochlea
11. Rods of actin filaments in type I hair cells of the Shaker 2 mouse
12. Sensory hairs and filaments rods in vestibular hair cells of the waltzing guinea pig. Organization and identification of actin
13. Immunohistochemical identification and localization of actin and fimbrin in vestibular hair cells in the normal guinea pig and in a strain of the waltzing guinea pig
14. Inherited hearing defects in mice
15. Hereditary inner-ear abnormalities in animals. Relationships with human abnormalities
16. Genetics of deafness