-
1
-
-
0028836920
-
A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17
-
(1995)
Nature Genet.
, vol.9
, pp. 86-91
-
-
Friedman, T.B.1
Liang, Y.2
Weber, J.L.3
Hinnant, J.T.4
Barber, T.D.5
Winata, S.6
Arhya, I.N.7
Asher, J.H.J.8
-
2
-
-
17344372052
-
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 904-915
-
-
Liang, Y.1
Wang, A.2
Probst, F.J.3
Arhya, I.N.4
Barber, T.D.5
Chen, K.S.6
Deshmukh, D.7
Dolan, D.F.8
Hinnant, J.T.9
Carter, L.E.10
-
3
-
-
17644442703
-
Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene
-
(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
-
4
-
-
0008367497
-
Linkage tests of the new shaker mutation with other factors in the house mouse (Mus musculus)
-
(1934)
Am. Nature
, vol.68
, pp. 173
-
-
Gates, W.H.1
-
6
-
-
0032729835
-
Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2
-
(1999)
Genomics
, vol.61
, pp. 243-258
-
-
Liang, Y.1
Wang, A.2
Belyantseva, I.A.3
Anderson, D.W.4
Probst, F.J.5
Barber, T.D.6
Miller, W.7
Touchman, J.W.8
Jin, L.9
Sullivan, S.L.10
-
8
-
-
0024284065
-
The drosophila ninaC locus encodes two photoreceptor cell specific proteins with domains homologous to protein kinases and the myosin heavy chain head
-
(1988)
Cell
, vol.52
, pp. 757-772
-
-
Montell, C.1
Rubin, G.M.2
-
10
-
-
1842296915
-
Synaptic vesicle endocytosis impaired by disruption of dynamin-SH3 domain interactions
-
(1997)
Science
, vol.276
, pp. 259-263
-
-
Shupliakov, O.1
Low, P.2
Grabs D.3
Gad, H.4
Chen, H.5
David, C.6
Takei, K.7
De Camilli, P.8
Brodin, L.9
-
11
-
-
0032526679
-
The Src homology domain 3 (SH3) of a yeast type I myosin, Myo5p, binds to verprolin and is required for targeting to sites of actin polarization
-
(1998)
J. Cell Biol.
, vol.141
, pp. 1357-1370
-
-
Anderson, B.L.1
Boldogh, I.2
Evangelista, M.3
Boone, C.4
Greene, L.A.5
Pon, L.A.6
-
12
-
-
0031683065
-
The FERM domain: A unique module involved in the linkage of cytoplasmic proteins to the membrane [letter]
-
(1998)
Trends Biochem. Sci.
, vol.23
, pp. 281-282
-
-
Chishti, A.H.1
Kim, A.C.2
Marfatia, S.M.3
Lutchman, M.4
Hanspal, M.5
Jindal, H.6
Liu, S.C.7
Low, P.S.8
Rouleau, G.A.9
Mohandas, N.10
-
13
-
-
0032559637
-
Ezrin/radixin/moesin (ERM) proteins bind to a positively charged amino acid cluster in the juxta-membrane cytoplasmic domain of CD44, CD43, and ICAM-2
-
(1998)
J. Cell Biol.
, vol.140
, pp. 885-895
-
-
Yonemura, S.1
Hirao, M.2
Doi, Y.3
Takahashi, N.4
Kondo, T.5
Tsukita, S.6
-
14
-
-
0030587490
-
Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B
-
(1996)
Genomics
, vol.36
, pp. 440-448
-
-
Chen, Z.Y.1
Hasson, T.2
Kelley, P.M.3
Schwender, B.J.4
Schwartz, M.F.5
Ramakrishnan, M.6
Kimberling, W.J.7
Mooseker, M.S.8
Corey, D.P.9
-
15
-
-
0031151953
-
Mutation analysis of the mouse myosin VIIA deafness gene
-
(1997)
Genes Funct.
, vol.1
, pp. 191-203
-
-
Mburu, P.1
Liu, X.Z.2
Walsh, J.3
Saw, D.J.4
Cope, M.J.5
Gibson, F.6
Kendrick-Jones, J.7
Steel, K.P.8
Brown, S.D.9
-
18
-
-
0032577293
-
Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3
-
(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
-
22
-
-
0028803112
-
The mouse snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
-
(1995)
Nature 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
-
23
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene shaker-1
-
(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.9
-
32
-
-
0003575881
-
The house mouse: Atlas of embryonic development
-
Springer-Verlag, New York, NY.
-
(1989)
-
-
Theiler, K.1
-
39
-
-
0000747819
-
The anomalies of the labyrinth of the mutants varitint-waddler, shaker-2 and jerker in the mouse
-
(1954)
J. Genet.
, vol.52
, pp. 562-588
-
-
Deol, M.S.1
|