-
1
-
-
0029807805
-
Genes responsible for human hereditary deafness: Symphony of a thousand
-
Petit, C. Genes responsible for human hereditary deafness: symphony of a thousand. Nature Genet. 14, 385-391 (1996).
-
(1996)
Nature Genet.
, vol.14
, pp. 385-391
-
-
Petit, C.1
-
2
-
-
0031443872
-
Otogelin: A glycoprotein specific to the acellular membranes of the inner ear
-
Cohen-Salmon, M., El-Amraoui, A., Leibovici, M. & Petit, C. Otogelin: a glycoprotein specific to the acellular membranes of the inner ear. Proc. Natl Acad. Sci. USA 94, 14450-14455 (1997).
-
(1997)
Proc. Natl Acad. Sci. USA
, vol.94
, pp. 14450-14455
-
-
Cohen-Salmon, M.1
El-Amraoui, A.2
Leibovici, M.3
Petit, C.4
-
3
-
-
0024433313
-
How the ear's works work
-
Hudspeth, A.J. How the ear's works work. Nature 341, 397-404 (1989).
-
(1989)
Nature
, vol.341
, pp. 397-404
-
-
Hudspeth, A.J.1
-
4
-
-
0025005344
-
Sodium arsanilate-induced vestibular dysfunction in rats: Effects of open-field behavior and spontaneous activity in the automated digiscan monitoring system
-
Ossenkopp, K.P., Prkacin, A. & Hargreaves, E.L. Sodium arsanilate-induced vestibular dysfunction in rats: effects of open-field behavior and spontaneous activity in the automated digiscan monitoring system. Pharmacol. Biochem. Behav. 36, 875-881 (1990).
-
(1990)
Pharmacol. Biochem. Behav.
, vol.36
, pp. 875-881
-
-
Ossenkopp, K.P.1
Prkacin, A.2
Hargreaves, E.L.3
-
5
-
-
0025108084
-
An open-field activity analysis of labyrinthectomized rats
-
Porter, J.D., Pellis, S.M. & Meyer, M.E. An open-field activity analysis of labyrinthectomized rats. Physiol. Behav. 48, 27-30 (1990).
-
(1990)
Physiol. Behav.
, vol.48
, pp. 27-30
-
-
Porter, J.D.1
Pellis, S.M.2
Meyer, M.E.3
-
6
-
-
0027491851
-
The behavioral syndrome caused by 3,3′-iminodipropionitrile and related nitriles in the rat is associated with degeneration of the vestibular sensory hair cells
-
Liorens, J., Dermenes, D. & Sans, A. The behavioral syndrome caused by 3,3′-iminodipropionitrile and related nitriles in the rat is associated with degeneration of the vestibular sensory hair cells. Toxicol. Applied Pharmacol. 123, 199-210 (1993).
-
(1993)
Toxicol. Applied Pharmacol.
, vol.123
, pp. 199-210
-
-
Liorens, J.1
Dermenes, D.2
Sans, A.3
-
7
-
-
0018386571
-
Auditory nerve and brain stem volume-conducted potentials by pure-tone pips in the CBA/J laboratory mouse
-
Henry, K.R. Auditory nerve and brain stem volume-conducted potentials by pure-tone pips in the CBA/J laboratory mouse. Audiology 18, 93-108 (1979).
-
(1979)
Audiology
, vol.18
, pp. 93-108
-
-
Henry, K.R.1
-
8
-
-
0030889074
-
The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system
-
Legan, P.K., Rau, A., Keen, J.N. & Richardson, G.P. The mouse tectorins. Modular matrix proteins of the inner ear homologous to components of the sperm-egg adhesion system. J. Biol. Chem. 272, 8791-8801 (1997).
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 8791-8801
-
-
Legan, P.K.1
Rau, A.2
Keen, J.N.3
Richardson, G.P.4
-
9
-
-
0033535316
-
Tectorin mRNA expression is spatially and temporally restricted during mouse inner ear development
-
Rau, A., Legan, P.K. & Richardson, G.P. Tectorin mRNA expression is spatially and temporally restricted during mouse inner ear development. J. Comp. Neurol. 405, 271-280 (1999).
-
(1999)
J. Comp. Neurol.
, vol.405
, pp. 271-280
-
-
Rau, A.1
Legan, P.K.2
Richardson, G.P.3
-
10
-
-
0028106530
-
Immunohistochemical localization of keratan sulfate and chondroitin 4- and 6-sulfate proteoglycans in subregions of the tectorial and basilar membranes
-
Munyer, P.D. & Schulte, B.A. Immunohistochemical localization of keratan sulfate and chondroitin 4- and 6-sulfate proteoglycans in subregions of the tectorial and basilar membranes. Hearing Res. 79, 83-93 (1994).
-
(1994)
Hearing Res.
, vol.79
, pp. 83-93
-
-
Munyer, P.D.1
Schulte, B.A.2
-
11
-
-
0015403485
-
Fine morphology of the tectorial membrane. Its relationship to the organ of Corti
-
Lim, D.J. Fine morphology of the tectorial membrane. Its relationship to the organ of Corti. Arch. Otolaryngol. 96, 199-215 (1972).
-
(1972)
Arch. Otolaryngol.
, vol.96
, pp. 199-215
-
-
Lim, D.J.1
-
12
-
-
0018172093
-
Ultrastructure of the different zones of the tectorial membrane
-
Kronester-Frei, A. Ultrastructure of the different zones of the tectorial membrane. Cell Tissue Res. 193, 11-23 (1978).
-
(1978)
Cell Tissue Res.
, vol.193
, pp. 11-23
-
-
Kronester-Frei, A.1
-
13
-
-
0023759376
-
The ultrastructural organization and properties of the mouse tectorial membrane matrix
-
Hasko, J.A. & Richardson, G.P. The ultrastructural organization and properties of the mouse tectorial membrane matrix. Hearing Res. 35, 21-38 (1988).
-
(1988)
Hearing Res.
, vol.35
, pp. 21-38
-
-
Hasko, J.A.1
Richardson, G.P.2
-
14
-
-
0030757333
-
Ultrastructure organization of proteoglycans and fibrillar matrix of the tectorial membrane
-
Tsuprun, V. & Santi, P. Ultrastructure organization of proteoglycans and fibrillar matrix of the tectorial membrane. Hearing Res. 110, 107-118 (1997).
-
(1997)
Hearing Res.
, vol.110
, pp. 107-118
-
-
Tsuprun, V.1
Santi, P.2
-
15
-
-
0026515616
-
Type II and type IX collagen form heterotypic fibers in the tectorial membrane of the inner ear
-
Slepecky, N.B., Cefaratti, L.K. & Yoo, T.J. Type II and type IX collagen form heterotypic fibers in the tectorial membrane of the inner ear. Matrix 12, 80-86 (1992).
-
(1992)
Matrix
, vol.12
, pp. 80-86
-
-
Slepecky, N.B.1
Cefaratti, L.K.2
Yoo, T.J.3
-
16
-
-
0026547507
-
Electron-microscopic localization of type II,IX and V collagen in the organ of corti
-
Slepecky, N.B., Savage, S.E., Cerafatti, L.K. & Yoo, T.J. Electron-microscopic localization of type II,IX and V collagen in the organ of Corti. Cell Tissue Res. 267, 413-418 (1992).
-
(1992)
Cell Tissue Res.
, vol.267
, pp. 413-418
-
-
Slepecky, N.B.1
Savage, S.E.2
Cerafatti, L.K.3
Yoo, T.J.4
-
17
-
-
0023895565
-
Tectorial membrane. I: Static mechanical properties in vivo
-
Zwislocki, J.J., Chamberlain, S.C. & Slepecky, N.B. Tectorial membrane. I: static mechanical properties in vivo. Hearing Res. 33, 207-222 (1988).
-
(1988)
Hearing Res.
, vol.33
, pp. 207-222
-
-
Zwislocki, J.J.1
Chamberlain, S.C.2
Slepecky, N.B.3
-
18
-
-
0028226978
-
Tightly linked flanking microsatellite markers for the usher syndrome type I locus on the short arm of chromosome 11
-
Keats, B.J., Noury, N., Pelias, M.Z., Deininger, P.L. & Litt, M. Tightly linked flanking microsatellite markers for the Usher syndrome type I locus on the short arm of chromosome 11. Am. J. Hum. Genet. 54, 681-686 (1994).
-
(1994)
Am. J. Hum. Genet.
, vol.54
, pp. 681-686
-
-
Keats, B.J.1
Noury, N.2
Pelias, M.Z.3
Deininger, P.L.4
Litt, M.5
-
19
-
-
0032104235
-
A gene responsible for nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene
-
Jain, P.K. et al. A gene responsible for nonsyndromic sensorineural deafness (DFNB18) maps to the chromosomal region 11p14-p15.1 containing the Usher syndrome type 1C gene. Genomics 50, 290-292 (1998).
-
(1998)
Genomics
, vol.50
, pp. 290-292
-
-
Jain, P.K.1
-
20
-
-
0032811509
-
Mapping of the otogelin gene (OTGN) to mouse chromosome 7 and human chromosome 11p14.3: A candidate for human autosomal recessive nonsyndromic deafness DFNB18
-
Cohen-Salmon, M., Mattei, M.-G. & Petit, C. Mapping of the otogelin gene (OTGN) to mouse chromosome 7 and human chromosome 11p14.3: a candidate for human autosomal recessive nonsyndromic deafness DFNB18. Mamm. Genome 10, 520-522 (1999).
-
(1999)
Mamm. Genome
, vol.10
, pp. 520-522
-
-
Cohen-Salmon, M.1
Mattei, M.-G.2
Petit, C.3
-
21
-
-
0031007349
-
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness
-
Kelsell, D.P. et al. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 387, 80-83 (1997).
-
(1997)
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
-
22
-
-
17344373747
-
Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment
-
Xia, J.-h. et al. Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment. Nature Genet. 20, 370-373 (1998).
-
(1998)
Nature Genet.
, vol.20
, pp. 370-373
-
-
Xia, J.-H.1
-
23
-
-
0033524936
-
KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness
-
Kubisch, C. et al. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell 96, 437-446 (1999).
-
(1999)
Cell
, vol.96
, pp. 437-446
-
-
Kubisch, C.1
-
24
-
-
85069240579
-
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
-
Grifa, A. et al. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus Nature Genet. 23, 16-18 (1999).
-
(1999)
Nature Genet.
, vol.23
, pp. 16-18
-
-
Grifa, A.1
-
25
-
-
0029450413
-
Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease
-
Cohen-Tannoudji, M. et al. Disruption of murine Hexa gene leads to enzymatic deficiency and to neuronal lysosomal storage, similar to that observed in Tay-Sachs disease. Mamm. Genome 6, 844-849 (1995).
-
(1995)
Mamm. Genome
, vol.6
, pp. 844-849
-
-
Cohen-Tannoudji, M.1
-
26
-
-
0033582330
-
Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals
-
Verpy, E., Leibovici, M. & Petit, C. Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals. Proc. Natl Acad. Sci. USA 96, 529-534 (1999).
-
(1999)
Proc. Natl Acad. Sci. USA
, vol.96
, pp. 529-534
-
-
Verpy, E.1
Leibovici, M.2
Petit, C.3
-
27
-
-
0029845831
-
lacZ mouse embryos
-
lacZ mouse embryos. Development 122, 3023-3033 (1996).
-
(1996)
Development
, vol.122
, pp. 3023-3033
-
-
Bernex, F.1
-
28
-
-
0002860064
-
Assessing hearing, vision and balance in mice
-
Soc. Neurosci. short course syllabus, Washington DC
-
Steel, K.P. & Hardisty, R. Assessing hearing, vision and balance in mice. in What's Wrong with My Mouse? New Interplays Between Mouse Genes and Behavior 26-38 (Soc. Neurosci. short course syllabus, Washington DC, 1996).
-
(1996)
What's Wrong with My Mouse? New Interplays Between Mouse Genes and Behavior
, pp. 26-38
-
-
Steel, K.P.1
Hardisty, R.2
-
29
-
-
0001633148
-
Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses
-
Zheng, Q.Y., Johnson, K.R. & Reway, L.C. Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses. Hearing Res. 130, 94-107 (1999).
-
(1999)
Hearing Res.
, vol.130
, pp. 94-107
-
-
Zheng, Q.Y.1
Johnson, K.R.2
Reway, L.C.3
-
30
-
-
0027392717
-
Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains
-
Erway, L.C., Willott, J.F., Archer, J.R. & Harrison, D.E. Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains. Hearing Res. 65, 125-132 (1993).
-
(1993)
Hearing Res.
, vol.65
, pp. 125-132
-
-
Erway, L.C.1
Willott, J.F.2
Archer, J.R.3
Harrison, D.E.4
|