-
1
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type IB
-
Weil, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M.D. et al. (1995) Defective myosin VIIA gene responsible for Usher syndrome type IB. Nature (London) 374, 60-61
-
(1995)
Nature (London)
, 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
-
2
-
-
18344404410
-
The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A)
-
Kelley, P.M., Weston, M.D., Chen, Z.Y., Orten, D.J., Hasson, T., Overbeck, L.D., Pinnt, J., Talmadge, C.B., Ing, P., Mooseker, M.S., Corey, D., Sumegi, J. & Kimberling, W.J. (1997) The genomic structure of the gene defective in Usher syndrome type Ib (MYO7A). Genomics 40, 73-79
-
(1997)
Genomics
, vol.40
, pp. 73-79
-
-
Kelley, P.M.1
Weston, M.D.2
Chen, Z.Y.3
Orten, D.J.4
Hasson, T.5
Overbeck, L.D.6
Pinnt, J.7
Talmadge, C.B.8
Ing, P.9
Mooseker, M.S.10
Corey, D.11
Sumegi, J.12
Kimberling, W.J.13
-
3
-
-
0030951102
-
The autosomal recessive isolated deafness, DFNB2, and the Usher IB syndrome are allelic defects of the myosin-VIIA gene
-
Weil, D., Kussel, P., Blanchard, S., Levy, G., Levi-Acobas, F., Drira, M., Ayadi, H. & Petit, C. (1997) The autosomal recessive isolated deafness, DFNB2, and the Usher IB syndrome are allelic defects of the myosin-VIIA gene. Nat. Genet. 16, 191-193
-
(1997)
Nat. Genet.
, vol.16
, pp. 191-193
-
-
Weil, D.1
Kussel, P.2
Blanchard, S.3
Levy, G.4
Levi-Acobas, F.5
Drira, M.6
Ayadi, H.7
Petit, C.8
-
4
-
-
0031750338
-
Myosin VIIa as a common component of cilia and microvilli
-
Wolfrum, U., Liu, X., Schmitt, A., Udovichenko, I.P. & Williams, D.S. (1998) Myosin VIIa as a common component of cilia and microvilli. Cell Motility Cytoskel. 40, 261-271
-
(1998)
Cell Motility Cytoskel.
, vol.40
, pp. 261-271
-
-
Wolfrum, U.1
Liu, X.2
Schmitt, A.3
Udovichenko, I.P.4
Williams, D.S.5
-
5
-
-
0030965704
-
Effects of shaker-I mutations on myosin-VIIa protein and mRNA expression
-
Hasson, T., Walsh, J., Cable, J., Mooseker, M.S., Brown, S.D. & Steel, K.P. (1997) Effects of shaker-I mutations on myosin-VIIa protein and mRNA expression. Cell Motility Cytoskel. 37, 127-138
-
(1997)
Cell Motility Cytoskel.
, vol.37
, pp. 127-138
-
-
Hasson, T.1
Walsh, J.2
Cable, J.3
Mooseker, M.S.4
Brown, S.D.5
Steel, K.P.6
-
6
-
-
0031278277
-
Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene
-
Liu, X.Z., Walsh, J., Tamagawa, Y., Kitamura, K., Nishizawa, M., Steel, K.P. & Brown, S.D. (1997) Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene. Nat. Genet. 17, 268-269
-
(1997)
Nat. Genet.
, vol.17
, pp. 268-269
-
-
Liu, X.Z.1
Walsh, J.2
Tamagawa, Y.3
Kitamura, K.4
Nishizawa, M.5
Steel, K.P.6
Brown, S.D.7
-
7
-
-
0030960855
-
Mutations in the myosin VIIA gene cause non-syndromic recessive deafness
-
Liu, X.Z., Walsh, J., Mburu, P., Kendrick-Jones, J., Cope, M.J., Steel, K.P. & Brown, S.D. (1997) Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nat. Genet. 16, 188-190
-
(1997)
Nat. Genet.
, vol.16
, pp. 188-190
-
-
Liu, X.Z.1
Walsh, J.2
Mburu, P.3
Kendrick-Jones, J.4
Cope, M.J.5
Steel, K.P.6
Brown, S.D.7
-
8
-
-
0032216552
-
Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome
-
Liu, X.Z., Hope, C., Walsh, J., Newton, V., Ke, X.M., Liang, C.Y., Xu, L.R., Zhou, J.M., Trump, D., Steel, K.P. et al. (1998) Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome [letter]. Am. J. Hum. Genet. 63, 909-912
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 909-912
-
-
Liu, X.Z.1
Hope, C.2
Walsh, J.3
Newton, V.4
Ke, X.M.5
Liang, C.Y.6
Xu, L.R.7
Zhou, J.M.8
Trump, D.9
Steel, K.P.10
-
9
-
-
15144351296
-
Conservation within the myosin motor domain: Implications for structure and function
-
Cope, M.J.T., Whisstock, J., Rayment, I. & Kendrick-Jones, J. (1996) Conservation within the myosin motor domain: implications for structure and function. Structure 4, 969-987
-
(1996)
Structure
, vol.4
, pp. 969-987
-
-
Cope, M.J.T.1
Whisstock, J.2
Rayment, I.3
Kendrick-Jones, J.4
-
10
-
-
0002624845
-
Spectrum of myosin VIIa mutations causing Usher syndrome type Ib
-
Weston, M.D., Carney, C.A., Rivedal, S.A. & Kimberling, W.J. (1998) Spectrum of myosin VIIa mutations causing Usher syndrome type Ib. Assoc. Res. Otolaryngol. Abstr. 21, 41
-
(1998)
Assoc. Res. Otolaryngol. Abstr.
, vol.21
, pp. 41
-
-
Weston, M.D.1
Carney, C.A.2
Rivedal, S.A.3
Kimberling, W.J.4
-
11
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene shaker-I
-
Gibson, F., Walsh, J., Mburu, P., Varela, A., Brown, K.A., Antonio, M., Beisel, K.W., Steel, K.P. & Brown, S.D. (1995) A type VII myosin encoded by the mouse deafness gene shaker-I. Nature (London) 374, 62-64
-
(1995)
Nature (London)
, 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.9
-
12
-
-
0001345615
-
Shaker, a new mutation of the house mouse (Mus musculus)
-
Lord, E.M. & Gates, W.H. (1929) Shaker, a new mutation of the house mouse (Mus musculus). Am. Nat. 63, 435-442
-
(1929)
Am. Nat.
, vol.63
, pp. 435-442
-
-
Lord, E.M.1
Gates, W.H.2
-
13
-
-
0030973305
-
Unconventional myosins in inner-ear sensory epithelia
-
Hasson, T., Gillespie, P.G., Garcia, J.A., MacDonald, R.B., Zhao, Y., Yee, A.G., Mooseker, M.S. & Corey, D.P. (1997) Unconventional myosins in inner-ear sensory epithelia. J. Cell Biol. 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.8
-
14
-
-
0028787263
-
Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type IB
-
Hasson, T., Heintzelman, M.B., Santos-Sacchi, J., Corey, D.P. & Mooseker, M.S. (1995) Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type IB. Proc. Natl. Acad. Sci. U.S.A. 92, 9815-9819
-
(1995)
Proc. Natl. Acad. Sci. U.S.A.
, vol.92
, pp. 9815-9819
-
-
Hasson, T.1
Heintzelman, M.B.2
Santos-Sacchi, J.3
Corey, D.P.4
Mooseker, M.S.5
-
15
-
-
0031770385
-
Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells
-
Xiang, M., Gao, W.Q., Hasson, T. & Shin, J.J. (1998) Requirement for Brn-3c in maturation and survival, but not in fate determination of inner ear hair cells. Development 125, 3935-3946
-
(1998)
Development
, vol.125
, pp. 3935-3946
-
-
Xiang, M.1
Gao, W.Q.2
Hasson, T.3
Shin, J.J.4
-
16
-
-
0031151953
-
Mutation analysis of the mouse myosin VIIA deafness gene
-
Mburu, P., Liu, X.Z., Walsh, J., Saw, Jr., D., Cope, M.J., Gibson, F., Kendrick-Jones, J., Steel, K.P. & Brown, S.D. (1997) Mutation analysis of the mouse myosin VIIA deafness gene. Genes Funct. I, 191-203
-
(1997)
Genes Funct.
, vol.1
, pp. 191-203
-
-
Mburu, P.1
Liu, X.Z.2
Walsh, J.3
Saw Jr., D.4
Cope, M.J.5
Gibson, F.6
Kendrick-Jones, J.7
Steel, K.P.8
Brown, S.D.9
-
17
-
-
0000870234
-
The anatomy and development of the mutants pirouette, shaker-I and waltzer in the mouse
-
Deol, M.S. (1956) The anatomy and development of the mutants pirouette, shaker-I and waltzer in the mouse. Proc. R. Soc. Lond. B 145, 206-213
-
(1956)
Proc. R. Soc. Lond. B
, vol.145
, pp. 206-213
-
-
Deol, M.S.1
-
18
-
-
0031884319
-
Shaker-I mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells
-
Self, T., Mahony, M., Fleming, J., Walsh, J., Brown, S.D. & Steel, K.P. (1998) Shaker-I mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells. Development 125, 557-566
-
(1998)
Development
, vol.125
, pp. 557-566
-
-
Self, T.1
Mahony, M.2
Fleming, J.3
Walsh, J.4
Brown, S.D.5
Steel, K.P.6
-
19
-
-
0028803112
-
The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
-
Avraham, K.B., Hasson, T., Steel, K.P., Kingsley, D.M., Russell, L.B., Mooseker, M.S., Copeland, N.G. & Jenkins, N.A. (1995) The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells. Nat. Genet. 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
Mooseker, M.S.6
Copeland, N.G.7
Jenkins, N.A.8
-
20
-
-
0030751937
-
Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice
-
Avraham, K.B., Hasson, T., Sobe, T., Balsara, B., Testa, J.R., Skvorak, A.B., Morton, C.C., Copeland, N.G. & Jenkins, N.A. (1997) Characterization of unconventional MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice. Hum. Mol. Genet. 6, 1225-1231
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1225-1231
-
-
Avraham, K.B.1
Hasson, T.2
Sobe, T.3
Balsara, B.4
Testa, J.R.5
Skvorak, A.B.6
Morton, C.C.7
Copeland, N.G.8
Jenkins, N.A.9
-
21
-
-
0033569707
-
Role of myosin VI in the differentiation of cochlear hair cells
-
20a. Self, T., Sobe, T., Copeland, N.G., Jenkins, N.A., Avraham, K.B. & Steel, K.P. (1999) Role of myosin VI in the differentiation of cochlear hair cells. Dev. Biol. 214, 331-341
-
(1999)
Dev. Biol.
, vol.214
, pp. 331-341
-
-
Self, T.1
Sobe, T.2
Copeland, N.G.3
Jenkins, N.A.4
Avraham, K.B.5
Steel, K.P.6
-
22
-
-
0029048771
-
The 95F unconventional myosin is required for proper organization of the Drosophila syncytial blastoderm
-
Mermall, V. & Miller, K.G. (1995) The 95F unconventional myosin is required for proper organization of the Drosophila syncytial blastoderm. J. Cell Biol. 129, 1575-1588
-
(1995)
J. Cell Biol.
, vol.129
, pp. 1575-1588
-
-
Mermall, V.1
Miller, K.G.2
-
23
-
-
0032577293
-
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3
-
Wang, A., Liang, Y., Fridell, R.A., Probst, F.J., Wilcox, E.R., Touchman, J.W., Morton, C.C., Morell, R.J., Noben-Trauth, K., Camper, S.A. & Friedman, T.B. (1998) Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3. Science 280, 1447-1451
-
(1998)
Science
, vol.280
, pp. 1447-1451
-
-
Wang, A.1
Liang, Y.2
Fridell, R.A.3
Probst, F.J.4
Wilcox, E.R.5
Touchman, J.W.6
Morton, C.C.7
Morell, R.J.8
Noben-Trauth, K.9
Camper, S.A.10
Friedman, T.B.11
-
24
-
-
17644442703
-
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
-
Probst, F.J., Fridell, R.A., Raphael, Y., Saunders, T.L., Wang, A., Liang, Y., Morell, R.J., Touchman, J.W., Lyons, R.H., Noben-Trauth, K., Friedman, T.B. & Camper, S.A. (1998) Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene. Science 280, 1444-1447
-
(1998)
Science
, vol.280
, pp. 1444-1447
-
-
Probst, F.J.1
Fridell, R.A.2
Raphael, Y.3
Saunders, T.L.4
Wang, A.5
Liang, Y.6
Morell, R.J.7
Touchman, J.W.8
Lyons, R.H.9
Noben-Trauth, K.10
Friedman, T.B.11
Camper, S.A.12
-
25
-
-
0003154314
-
Molecular cloning of myosins from bullfrog saccular macula: A canidate for the hair-cell adaptation motor
-
Solc, C.K., Derfler, B.H., Duyk, G.M. & Corey, D.P. (1994) Molecular cloning of myosins from bullfrog saccular macula: a canidate for the hair-cell adaptation motor. Auditory Neurosci. 1, 63-75
-
(1994)
Auditory Neurosci.
, vol.1
, pp. 63-75
-
-
Solc, C.K.1
Derfler, B.H.2
Duyk, G.M.3
Corey, D.P.4
-
26
-
-
0031106188
-
Cloning of the genes encoding two murine and human cochlear unconventional type I myosins
-
Crozet, F., el Amraoui, A., Blanchard, S., Lenoir, M., Ripoll, C., Vago, P., Hamel, C., Fizames, C., Levi-Acobas, F., Depetris, D., Mattei, M.G. et al. (1997) Cloning of the genes encoding two murine and human cochlear unconventional type I myosins. Genomics 40, 332-341
-
(1997)
Genomics
, vol.40
, pp. 332-341
-
-
Crozet, F.1
El Amraoui, A.2
Blanchard, S.3
Lenoir, M.4
Ripoll, C.5
Vago, P.6
Hamel, C.7
Fizames, C.8
Levi-Acobas, F.9
Depetris, D.10
Mattei, M.G.11
-
27
-
-
0032525347
-
Myosin I beta is located at tip link anchors in vestibular hair bundles
-
Steyger, P.S., Gillespie, P.G. & Baird, R.A. (1998) Myosin I beta is located at tip link anchors in vestibular hair bundles. J. Neurosci. 18, 4603-4615
-
(1998)
J. Neurosci.
, vol.18
, pp. 4603-4615
-
-
Steyger, P.S.1
Gillespie, P.G.2
Baird, R.A.3
-
28
-
-
0032194948
-
Localization of myosin I beta near both ends of tip links in frog saccular hair cells
-
Garcia, J.A., Yee, A.G., Gillespie, P.G. & Corey, D.P. (1998) Localization of myosin I beta near both ends of tip links in frog saccular hair cells. J. Neurosci. 18, 8637-8647
-
(1998)
J. Neurosci.
, vol.18
, pp. 8637-8647
-
-
Garcia, J.A.1
Yee, A.G.2
Gillespie, P.G.3
Corey, D.P.4
-
29
-
-
0031612929
-
Recommendations for a nomenclature system for human gene mutations
-
Antonarakis, S.E. & Nomenclature Working Group (1998) Recommendations for a nomenclature system for human gene mutations. Hum. Mut. 11, 1-3
-
(1998)
Hum. Mut.
, vol.11
, pp. 1-3
-
-
Antonarakis, S.E.1
|