-
1
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene shaker-1
-
Gibson F, Walsh J, Mburu P, Varela A, Brown KA, Antonio M, Beisel KW, Steel KP, Brown SDM: A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 1995, 374:62-64.
-
(1995)
Nature
, vol.374
, pp. 62-64
-
-
Gibson, F.1
Walsh, J.2
Mburu, P.3
Varela, A.4
Brown, K.A.5
Antonio, M.6
Beisel, K.W.7
Steel, K.P.8
Brown, S.D.M.9
-
2
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type 1B
-
Weil D, Blanchard S, Kaplan J, Guilford P, Gibson F, Walsh J, Mburu P, Varela A, Levilliers J, Weston MD, et al.: Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 1995, 374:60-61.
-
(1995)
Nature
, vol.374
, pp. 60-61
-
-
Weil, D.1
Blanchard, S.2
Kaplan, J.3
Guilford, P.4
Gibson, F.5
Walsh, J.6
Mburu, P.7
Varela, A.8
Levilliers, J.9
Weston, M.D.10
-
3
-
-
0030973305
-
Unconventional myosins in inner-ear sensory epithelia
-
Hasson T, Gillespie PG, Garcia JA, MacDonald RB, Zhao Y, Yee AG, Mooseker MS, Corey DP Corey, Gillepsie PG: Unconventional myosins in inner-ear sensory epithelia. J Cell Biol 1997, 137:1287-1307.
-
(1997)
J Cell Biol
, vol.137
, pp. 1287-1307
-
-
Hasson, T.1
Gillespie, P.G.2
Garcia, J.A.3
MacDonald, R.B.4
Zhao, Y.5
Yee, A.G.6
Mooseker, M.S.7
Corey, D.P.C.8
Gillepsie, P.G.9
-
4
-
-
0031467787
-
Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cells
-
Richardson GP, Forge A, Kros CJ, Fleming J, Brown SD, Steel KP: Myosin VIIA is required for aminoglycoside accumulation in cochlear hair cells. J Neurosci 1997, 17:9506-951 9.
-
(1997)
J Neurosci
, vol.17
, pp. 9506-9519
-
-
Richardson, G.P.1
Forge, A.2
Kros, C.J.3
Fleming, J.4
Brown, S.D.5
Steel, K.P.6
-
5
-
-
0028803112
-
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
-
Avraham KB, Hasson T, Steel KP, Kingsley DM, Russell LB, Moosekar MS, Copeland NG, Jenkins NA: The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells. Nat Genet 1995, 11:369-375.
-
(1995)
Nat Genet
, vol.11
, pp. 369-375
-
-
Avraham, K.B.1
Hasson, T.2
Steel, K.P.3
Kingsley, D.M.4
Russell, L.B.5
Moosekar, M.S.6
Copeland, N.G.7
Jenkins, N.A.8
-
6
-
-
0031007349
-
Connexin 26 mutations in hereditary nonsyndromic sensorineural deafness
-
Kelsell DP, Dunlop J, Stevens HP, Lench NJ, Liang JN, Parry G, Mueller RF, Leigh IM: Connexin 26 mutations in hereditary nonsyndromic sensorineural deafness. Nature 387:80-83.
-
Nature
, vol.387
, pp. 80-83
-
-
Kelsell, D.P.1
Dunlop, J.2
Stevens, H.P.3
Lench, N.J.4
Liang, J.N.5
Parry, G.6
Mueller, R.F.7
Leigh, I.M.8
-
7
-
-
0030707797
-
Nonsyndromic deafness DFNA1 associated with mutation of the human homolog HDIA1 of the Drosophila diaphanous gene
-
Lynch ED, Lee MK, Morrow JE, Welsh PL, Leon PE, King MC: Nonsyndromic deafness DFNA1 associated with mutation of the human homolog HDIA1 of the Drosophila diaphanous gene. Science 1997, 278:1315-1318.
-
(1997)
Science
, vol.278
, pp. 1315-1318
-
-
Lynch, E.D.1
Lee, M.K.2
Morrow, J.E.3
Welsh, P.L.4
Leon, P.E.5
King, M.C.6
-
8
-
-
7144257859
-
Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans
-
Vahava O, Morell R, Lynch ED, Weiss S, Kagan ME, Ahituv N, Morrow JE, Lee MK, Skvorak AB, Morton CC, et al.: Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science 1998, 279:1950-1954.
-
(1998)
Science
, vol.279
, pp. 1950-1954
-
-
Vahava, O.1
Morell, R.2
Lynch, E.D.3
Weiss, S.4
Kagan, M.E.5
Ahituv, N.6
Morrow, J.E.7
Lee, M.K.8
Skvorak, A.B.9
Morton, C.C.10
-
9
-
-
0030134593
-
Touch at the molecular level: Mechanosensation
-
Garcia-Anoveros J, Corey DP: Touch at the molecular level: Mechanosensation. Curr Biol 1996, 6:541-543.
-
(1996)
Curr Biol
, vol.6
, pp. 541-543
-
-
Garcia-Anoveros, J.1
Corey, D.P.2
-
10
-
-
0030042571
-
Early ear development in the embryo of the zebrafish, Danio rerio
-
Haddon C, Lewis J: Early ear development in the embryo of the zebrafish, Danio rerio. J Comp Neurol 1996, 365:113-128.
-
(1996)
J Comp Neurol
, vol.365
, pp. 113-128
-
-
Haddon, C.1
Lewis, J.2
-
11
-
-
12644251056
-
Mutations affecting development of the zebrafish inner ear and lateral line
-
Whitfield TT, Granato M, van Eeden FJ, Schach U, Brand M, Furutani-Seiki M, Haffter P, Hammerschmidt M, Heisenberg CP, Jiang YJ, et al.: Mutations affecting development of the zebrafish inner ear and lateral line. Development 1996, 123:241-254.
-
(1996)
Development
, vol.123
, pp. 241-254
-
-
Whitfield, T.T.1
Granato, M.2
Van Eeden, F.J.3
Schach, U.4
Brand, M.5
Furutani-Seiki, M.6
Haffter, P.7
Hammerschmidt, M.8
Heisenberg, C.P.9
Jiang, Y.J.10
-
12
-
-
0032006996
-
Genetic analysis of vertebrate sensory hair cell mechanosensation: The zebrafish circler mutants
-
Nicolson T, Rusch A, Friedrich RW, Granato M, Ruppersberg JP, Nusslein-Volhard C: Genetic analysis of vertebrate sensory hair cell mechanosensation: the zebrafish circler mutants. Neuron 1998, 20:271-283.
-
(1998)
Neuron
, vol.20
, pp. 271-283
-
-
Nicolson, T.1
Rusch, A.2
Friedrich, R.W.3
Granato, M.4
Ruppersberg, J.P.5
Nusslein-Volhard, C.6
-
13
-
-
0031887992
-
Zebrafish hox genes: Genomic organization and modified colinear expression patterns in the trunk
-
Prince VE, Joly L, Ekker M, Ho RK: Zebrafish hox genes: genomic organization and modified colinear expression patterns in the trunk. Development 1998, 125:407-420.
-
(1998)
Development
, vol.125
, pp. 407-420
-
-
Prince, V.E.1
Joly, L.2
Ekker, M.3
Ho, R.K.4
|