Biology Reference
In-Depth Information
Vetter DE, Mann JR, Wangemann P, Liu J, et al. (1996) Inner ear defects induced
by null mutation of the isk gene. Neuron 17:1251-1264.
Wang W, Van de Water T, Lufkin T (1998) Inner ear and maternal reproductive
defects in mice lacking the Hmx3 homeobox gene. Dev 125:621-634.
Wang H, Allen ML, Grigg JJ, Noebels JL, Tempel BL (1995) Hypomyelination alters
K + channel expression in mouse mutants shiverer and trembler. Neuron 15:
1337-1347.
Wang A, Liang Y, Fridell RA, Probst FJ, et al. (1998) Association of unconventional
myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science
280:1447-1451.
Watanabe H, Kimata K, Line S, Strong D, et al. (1994) Mouse cartilage matrix
deficiency ( cmd ) caused by a 7 bp deletion in the aggrecan gene. Nat Genet
7:154-157.
Watanabe H, Yamada Y (1999) Mice lacking link protein develop dwarfism and
craniofacial abnormalities. Nat Genet 21:225-229.
Watanabe-Fukunaga R, Brannan CI, Copeland NG, Jenkins NA, Nagata S (1992)
Lymphoproliferation disorder in mice explained by defects in Fas antigen that
mediates apoptosis. Nature 356:314-317.
Wehr R, Mansouri A, de Maeyer T, Gruss P (1997) Fkh5 -deficient mice show
dysgenesis in the caudal midbrain and hypothalamic mammillary body. Dev 124:
4447-4456.
Weil D, Blanchard S, Kaplan J, Guilford P, et al. (1995) Defective myosin VIIA gene
responsible for Usher syndrome type 1B. Nature 374:60-61.
Weil D, Kussel P, Blanchard S, Levy G, et al. (1997) The autosomal recessive iso-
lated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the
myosin-VIIA gene. Nat Genet 16:191-193.
Wenngren B-I, Anniko M (1988) Age-related auditory brainstem response (ABR)
threshold changes in the dancer mouse mutant. Acta Otolaryng 106:386-392.
Wenngren B-I, Anniko M (1990) Aberrant frequency tuning and early stereociliary
derangement in genetic inner ear disease. Acta Otolaryng 109:202-212.
Whitlon DS, Gabel C, Zhang X (1996) Cochlear inner hair cells exist transiently in
the fetal Bronx Waltzer ( bv/bv ) mouse. J Comp Neurol 364:515-522.
Whitlon DS, Sobkowicz HM (1991) Patterns of hair cell survival and innervation in
the cochlea of the Bronx waltzer mouse. J. Neurocytol 20:886-901.
Willott JF, Erway LC (1998) Genetics of age-related hearing loss in mice. IV.
Cochlear pathology and hearing loss in 25 BXD recombinant inbred mouse
strains. Hear Res 119:27-36.
Wilson DB (1985) An ultrastructural analysis of abnormal otic development in
exencephalic mutant mice. Arch Otorhinolaryng 241:203-208.
Wilson DB, Wyatt DP (1995) Alterations in cranial morphogenesis in the Lp mutant
mouse. J Craniofac Genet Dev Biol 15:182-189.
Winograd J, Reilly MP, Roe R, Lutz J, et al. (1997) Perinatal lethality and multiple
craniofacial malformations in MSX2 transgenic mice. Hum Molec Genet 6:
369-379.
Wright CG, Robinson KS, Comerford SA (1995) Transforming growth factor alpha
in the adult mammalian inner ear. ARO Abstracts 18:109.
Xia JH, Liu CY, Tang BS, Pan Q, et al. (1998) Mutations in the gene encoding gap
junction protein beta-3 associated with autosomal dominant hearing impairment.
Nat Genet 20:370-373.
Search WWH ::




Custom Search