Biology Reference
In-Depth Information
Cable J, Barkway C, Steel KP (1992) Characteristics of stria vascularis melanocytes
of viable dominant spotting ( W v /W v ) mouse mutants. Hear Res 64:6-20.
Cable J, Huszar D, Jaenisch R, Steel KP (1994) Effects of mutations at the W locus
( c-kit ) on inner ear pigmentation and function in the mouse. Pigm Cell Res
7:17-32.
Cable J, Jackson IJ, Steel KP (1993) Light ( B lt ), a mutation causing melanocyte
death, leads to strial dysfunction in the inner ear. Pigm Cell Res 6:215-225.
Cable J, Jackson IJ, Steel KP (1995) Mutations at the W locus affect survival of
neural crest-derived melanocytes in the mouse. Mech Dev 50:139-150.
Cable J, Steel KP (1991) Identification of two types of melanocyte within the stria
vascularis of the mouse inner ear. Pigment Cell Res 4:87-101.
Cable J, Steel KP (1998) Combined cochleo-saccular and neuroepithelial abnor-
malities in the Varitint-waddler-J ( Va J ) mouse. Hear Res 123:125-136.
Campos Barros A, Erway LC, Krezel W, Curran T, et al. (1998) Absence of thyroid
hormone receptor b-retinoid X receptor interactions in auditory function and in
the pituitary-thyroid axis. Neuroreport 9:2933-2937.
Chabot B, Stephenson DA, Chapman VM, Besmer P, Bernstein A (1988) The proto-
oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the
mouse W locus. Nature 335:88-89.
Chai CK, Chiang MSM (1962) The inheritance of careener, unbalanced locomotion
in mice. Genetics 47:435-441.
Chan E, Baron S, Wang W, Lufkin T, Van De Water T (2000) Vestibular defects in
mice lacking the Hmx2 homeobox gene: Embryonic day 14.5 to birth. ARO
Abstracts 23:192.
Chen P, Segil N (1999) p27 Kip1 links cell proliferation to morphogenesis in the
developing organ of Corti. Dev 126:1581-1590.
Chisaka O, Musci TS, Capecchi MR (1992) Developmental defects of the ear, cranial
nerves and hindbrain resulting from targeted disruption of the mouse homeobox
gene Hox-1.6 . Nature 355:516-520.
Clouthier DE, Hosoda K, Richardson JA, Williams SC, et al. (1998) Cranial and
cardiac neural crest defects in endothelin-A receptor-deficient mice. Dev 125:
813-824.
Colvin JS, Bohne BA, Harding GW, McEwen DG, Ornitz DM (1996) Skeletal over-
growth and deafness in mice lacking fibroblast growth factor receptor 3. Nat
Genet 12:390-397.
Conlee JW, Jensen RP, Parks TN, Creel DJ (1991) Turn-specific and pigment-
dependent differences in the stria vascularis of normal and gentamicin-treated
albino and pigmented guinea pigs. Hear Res 55:57-69.
Copeland NG, Gilbert KJ, Cho BC, Donovan PJ, et al. (1990) Mast cell growth factor
maps near the steel locus on mouse chromosome 10 and is deleted in a number
of steel alleles. Cell 63:175-183.
Cordes SP, Barsh GS (1994) The mouse segmentation gene kr encodes a novel basic
domain-leucine zipper transciption factor. Cell 79:1025-1034.
Cosgrove D, Samuelson G, Meehan DT, Miller C, et al. (1998) Ultrastructural,
physiological, and molecular defects in the inner ear of a gene-knockout mouse
model for autosomal Alport syndrome. Hear Res 121:84-98.
Creel D, Conlee JW, Parks TN (1983) Auditory brainstem anomalies in albino cats.
I. Evoked potential studies. Brain Res 260:1-9.
Search WWH ::




Custom Search