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Qiu M, Bulfone A, Ghattas I, Meneses JJ, et al. (1997) Role of the Dlx homeobox
genes in proximodistal patterning of the branchial arches: Mutations of Dlx-1 ,
Dlx-2 , and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue
structures derived from the first and second arches. Dev Biol 185:165-184.
Rask-Andersen H, Erwall C, Steel KP, Friberg U (1987) The endolymphatic sac in
a mouse mutant with cochleo-saccular degeneration. Hear Res 26:177-190.
Rauch SD (1992) Malformation and degeneration in the inner ear of mos trans-
genic mice. Ann Otol Rhinol Laryngol 101:430-436.
Rayner EM, Mulroy MJ (1997) Sensorineural hearing loss in the mdx mouse: A
model of Duchenne muscular dystrophy. Laryngoscope 107:1053-1056.
Refetoff S, DeWind LT, DeGroot LJ (1967) Familial syndrome combining deaf-
mutism, stuppled epiphyses, goiter and abnormally high PBI: Possible target organ
refractoriness to thyroid hormone. J Clin Endocrinol Metab 27:279-294.
Reimer K, Urbánek P, Busslinger M, Ehret G (1996) Normal brainstem auditory
evoked potentials in Pax 5 -deficient mice despite morphologic alterations in the
auditory midbrain region. Audiology 35:55-61.
Reimold AM, Grusby MJ, Kosaras B, Fries JWU, et al. (1996) Chondrodysplasia and
neurological abnormalities in ATF-2-deficient mice. Nature 379:262-265.
Reuter A, Nestl A, Zwacka RM, Tuckermann J, et al. •• Expression of the recessive
glomerulosclerosis gene Mpv17 regulates MMP-2 expression in fibroblasts, the
kidney, and the inner ear of mice. Mol Biol Cell 9:1675-1682.
Richardson GP, Forge A, Kros CJ, Fleming J, Brown SDM, Steel KP (1997)
Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cells.
J Neurosci 17:9506-9519.
Rijli FM, Mark M, Lakkaraju S, Dierich A, Dollé P, Chambon P (1993) A homeotic
transformation is generated in the rostral branchial region of the head by dis-
ruption of Hoxa-2 , which acts as a selector gene. Cell 75:1333-1349.
Rivera-Pérez JA, Mallo M, Gengron-Maguire M, Gridley T, Behringer RR (1995)
goosecoid is not an essential component of the mouse gastrula organizer but is
required for craniofacial and rib development. Dev 121:3005-3012.
Rio C, Adams JC, Liberman MC, Corfas G (1999) Loss of cochlear neurons in trans-
genic mice expressing a dominant negative erb4 receptor under the control of the
GFAP promotor. ARO abstracts. 22:138.
Robertson NG, Lu L, Heller S, Merchant SN, et al. (1998) Mutations in a novel
cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular
dysfunction. Nat Genet 20:299-303.
Rolfsen RM, Erway LC (1984) Trace metals and otolith defects in mocha mice. J
Hered 75:158-162.
Rossel M, Capecchi MR (1999) Mice mutant for both Hoxa1 and Hoxb1 show
extensive remodeling of the hindbrain and defects in craniofacial development.
Dev 126:5027-5040.
Ruben RJ (1973) Development and cell kinetics of the kreisler ( kr/kr ) mouse.
Laryngoscope 83:1440-1468.
Ruckenstein MJ, Mount RJ, Harrison RV (1993) The MRL- lpr/lpr mouse: A poten-
tial model of autoimmune inner ear disease. Acta Otolaryng 113:160-165.
Rüsch A, Erway LC, Oliver D, Vennstrom B, Forrest D (1998) Thyroid hormone
receptor b-dependent expression of a potassium conductance in inner hair cells
at the onset of hearing. Proc Natl Acad Sci USA 95:15758-15762.
Salminen M, Meyer BI, Bober E, Gruss P (2000) Netrin 1 is required for semicircular
canal formation in the mouse inner ear. Dev 127:13-22.
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