-
2
-
-
0033619258
-
Myosin VI is an actin-based motor that moves backwards
-
Wells AL, Lin AW, Chen LQ, et al. Myosin VI is an actin-based motor that moves backwards. Nature. 1999; 401: 505-508.
-
(1999)
Nature
, vol.401
, pp. 505-508
-
-
Wells, A.L.1
Lin, A.W.2
Chen, L.Q.3
-
3
-
-
0013985845
-
Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse
-
Deol MS, Green MC. Snell's waltzer, a new mutation affecting behaviour and the inner ear in the mouse. Genet Res. 1966; 8: 339-345.
-
(1966)
Genet Res
, vol.8
, pp. 339-345
-
-
Deol, M.S.1
Green, M.C.2
-
4
-
-
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, et al. 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
-
5
-
-
0029895005
-
Vertebrate unconventional myosins
-
Hasson T, Mooseker MS. Vertebrate unconventional myosins. J Biol Chem. 1996; 271: 16434.
-
(1996)
J Biol Chem
, vol.271
, pp. 16434
-
-
Hasson, T.1
Mooseker, M.S.2
-
6
-
-
0034887805
-
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss
-
Melchionda S, Ahituv N, Bisceglia L, et al. MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss. Am J Hum Genet. 2001; 69: 635-640.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 635-640
-
-
Melchionda, S.1
Ahituv, N.2
Bisceglia, L.3
-
7
-
-
0037730096
-
Mutations of MYO6 are associated with recessive deafness, DFNB37
-
Ahmed ZM, Morell RJ, Riazuddin S, et al. Mutations of MYO6 are associated with recessive deafness, DFNB37. Am J Hum Genet. 2003; 72: 1315-1322.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1315-1322
-
-
Ahmed, Z.M.1
Morell, R.J.2
Riazuddin, S.3
-
8
-
-
1942437588
-
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6)
-
Mohiddin SA, Ahmed ZM, Griffith AJ, et al. Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6). J Med Genet. 2004; 41: 309-314.
-
(2004)
J Med Genet
, vol.41
, pp. 309-314
-
-
Mohiddin, S.A.1
Ahmed, Z.M.2
Griffith, A.J.3
-
9
-
-
42949161087
-
A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family
-
Sanggaard KM, Kjaer KW, Eiberg H, et al. A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family. Am J Med Genet A. 2008; 146A: 1017-1025.
-
(2008)
Am J Med Genet A
, vol.146 A
, pp. 1017-1025
-
-
Sanggaard, K.M.1
Kjaer, K.W.2
Eiberg, H.3
-
10
-
-
17844406369
-
Nuclear and mitochondrial genes mutated in nonsyndromic impaired hearing
-
Finsterer J, Fellinger J. Nuclear and mitochondrial genes mutated in nonsyndromic impaired hearing. Int J Pediatr Otorhinolaryngol. 2005; 69: 621-647.
-
(2005)
Int J Pediatr Otorhinolaryngol
, vol.69
, pp. 621-647
-
-
Finsterer, J.1
Fellinger, J.2
-
11
-
-
0033967308
-
Novel myosin VI isoform is abundantly expressed in retina
-
Breckler J, Au K, Cheng J, Hasson T, Burnside B. Novel myosin VI isoform is abundantly expressed in retina. Exp Eye Res. 2000; 70: 121-134.
-
(2000)
Exp Eye Res
, vol.70
, pp. 121-134
-
-
Breckler, J.1
Au, K.2
Cheng, J.3
Hasson, T.4
Burnside, B.5
-
12
-
-
20544453606
-
Myosin VI is required for normal retinal function
-
Kitamoto J, Libby RT, Gibbs D, Steel KP, Williams DS. Myosin VI is required for normal retinal function. Exp Eye Res. 2005; 81: 116-120.
-
(2005)
Exp Eye Res
, vol.81
, pp. 116-120
-
-
Kitamoto, J.1
Libby, R.T.2
Gibbs, D.3
Steel, K.P.4
Williams, D.S.5
-
13
-
-
64049113787
-
Identification and localization of myosin superfamily members in fish retina and retinal pigmented epithelium
-
Lin-Jones J, Sohlberg L, Dose A, Breckler J, Hillman DW, Burnside B. Identification and localization of myosin superfamily members in fish retina and retinal pigmented epithelium. J Comp Neurol. 2009; 513: 209-223.
-
(2009)
J Comp Neurol
, vol.513
, pp. 209-223
-
-
Lin-Jones, J.1
Sohlberg, L.2
Dose, A.3
Breckler, J.4
Hillman, D.W.5
Burnside, B.6
-
14
-
-
0026801481
-
Association of myosin with the connecting cilium of rod photoreceptors
-
Williams DS, Hallett MA, Arikawa K. Association of myosin with the connecting cilium of rod photoreceptors. J Cell Sci. 1992; 103(pt 1): 183-190.
-
(1992)
J Cell Sci
, vol.103
, Issue.PART 1
, pp. 183-190
-
-
Williams, D.S.1
Hallett, M.A.2
Arikawa, K.3
-
15
-
-
77950650456
-
Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse
-
Mochizuki E, Okumura K, Ishikawa M, et al. Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse. Exp Anim. 2010; 59: 57-71.
-
(2010)
Exp Anim
, vol.59
, pp. 57-71
-
-
Mochizuki, E.1
Okumura, K.2
Ishikawa, M.3
-
16
-
-
2342512884
-
Uncoated endocytic vesicles require the unconventional myosin, Myo6, for rapid transport through actin barriers
-
Aschenbrenner L, Naccache SN, Hasson T. Uncoated endocytic vesicles require the unconventional myosin, Myo6, for rapid transport through actin barriers. Mol Biol Cell. 2004; 15: 2253-2263.
-
(2004)
Mol Biol Cell
, vol.15
, pp. 2253-2263
-
-
Aschenbrenner, L.1
Naccache, S.N.2
Hasson, T.3
-
17
-
-
0038107500
-
Myo6 facilitates the translocation of endocytic vesicles from cell peripheries
-
Aschenbrenner L, Lee T, Hasson T. Myo6 facilitates the translocation of endocytic vesicles from cell peripheries. Mol Biol Cell. 2003; 14: 2728-2743.
-
(2003)
Mol Biol Cell
, vol.14
, pp. 2728-2743
-
-
Aschenbrenner, L.1
Lee, T.2
Hasson, T.3
-
18
-
-
31544450256
-
Full-length myosin VI dimerizes and moves processively along actin filaments upon monomer clustering
-
Park H, Ramamurthy B, Travaglia M, et al. Full-length myosin VI dimerizes and moves processively along actin filaments upon monomer clustering. Mol Cell. 2006; 21: 331-336.
-
(2006)
Mol Cell
, vol.21
, pp. 331-336
-
-
Park, H.1
Ramamurthy, B.2
Travaglia, M.3
-
20
-
-
83055187553
-
Mouse model resources for vision research [serial online]
-
2011 Available at, Accessed October 11, 2013
-
Won J, Shi LY, Hicks W, et al. Mouse model resources for vision research [serial online]. J Ophthalmol. 2011; 2011: 391384. Available at: http://www. ncbi. nlm. nih. gov/pmc/articles/PMC2968714/. Accessed October 11, 2013.
-
(2011)
J Ophthalmol
, pp. 391384
-
-
Won, J.1
Shi, L.Y.2
Hicks, W.3
-
22
-
-
0036478946
-
Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis
-
Herron BJ, Lu W, Rao C, et al. Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis. Nat Genet. 2002; 30: 185-189.
-
(2002)
Nat Genet
, vol.30
, pp. 185-189
-
-
Herron, B.J.1
Lu, W.2
Rao, C.3
-
23
-
-
0021980329
-
Isolation of DNA from biological specimens without extraction with phenol
-
Buffone GJ, Darlington GJ. Isolation of DNA from biological specimens without extraction with phenol. Clin Chem. 1985; 31: 164-165.
-
(1985)
Clin Chem
, vol.31
, pp. 164-165
-
-
Buffone, G.J.1
Darlington, G.J.2
-
24
-
-
77954448094
-
Light-evoked responses of the retinal pigment epithelium: Changes accompanying photoreceptor loss in the mouse
-
Samuels IS, Sturgill GM, Grossman GH, Rayborn ME, Hollyfield JG, Peachey NS. Light-evoked responses of the retinal pigment epithelium: changes accompanying photoreceptor loss in the mouse. J Neurophysiol. 2010; 104: 391-402.
-
(2010)
J Neurophysiol
, vol.104
, pp. 391-402
-
-
Samuels, I.S.1
Sturgill, G.M.2
Grossman, G.H.3
Rayborn, M.E.4
Hollyfield, J.G.5
Peachey, N.S.6
-
25
-
-
33646144314
-
Functional abnormalities in the retinal pigment epithelium of CFTR mutant mice
-
Wu J, Marmorstein AD, Peachey NS. Functional abnormalities in the retinal pigment epithelium of CFTR mutant mice. Exp Eye Res. 2006; 83: 424-428.
-
(2006)
Exp Eye Res
, vol.83
, pp. 424-428
-
-
Wu, J.1
Marmorstein, A.D.2
Peachey, N.S.3
-
26
-
-
0027993176
-
Porcine myosin-VI: Characterization of a new mammalian unconventional myosin
-
Hasson T, Mooseker MS. Porcine myosin-VI: characterization of a new mammalian unconventional myosin. J Cell Biol. 1994; 127: 425-440.
-
(1994)
J Cell Biol
, vol.127
, pp. 425-440
-
-
Hasson, T.1
Mooseker, M.S.2
-
27
-
-
0346750740
-
Myosin function in nervous and sensory systems
-
Brown ME, Bridgman PC. Myosin function in nervous and sensory systems. J Neurobiol. 2004; 58: 118-130.
-
(2004)
J Neurobiol
, vol.58
, pp. 118-130
-
-
Brown, M.E.1
Bridgman, P.C.2
-
28
-
-
55249098639
-
A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells [serial online]
-
Available at, Accessed October 13, 2013
-
Hertzano R, Shalit E, Rzadzinska AK, et al. A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells [serial online]. PLoS Genet. 2008; 4: e1000207. Available at: http://www. ncbi. nlm. nih. gov/pmc/articles/PMC2543112/. Accessed October 13, 2013.
-
(2008)
PLoS Genet
, vol.4
-
-
Hertzano, R.1
Shalit, E.2
Rzadzinska, A.K.3
-
29
-
-
0033569707
-
Role of myosin VI in the differentiation of cochlear hair cells
-
Self T, Sobe T, Copeland NG, Jenkins NA, Avraham KB, Steel KP. Role of myosin VI in the differentiation of cochlear hair cells. Dev Biol. 1999; 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
-
30
-
-
0030846814
-
Unconventional myosins, the basis for deafness in mouse and man
-
Hasson T. Unconventional myosins, the basis for deafness in mouse and man. Am J Hum Genet. 1997; 61: 801-805.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 801-805
-
-
Hasson, T.1
-
31
-
-
0030780919
-
The growing family of myosin motors and their role in neurons and sensory cells
-
Hasson T, Mooseker MS. The growing family of myosin motors and their role in neurons and sensory cells. Curr Opin Neurobiol. 1997; 7: 615-623.
-
(1997)
Curr Opin Neurobiol
, vol.7
, pp. 615-623
-
-
Hasson, T.1
Mooseker, M.S.2
-
32
-
-
84876423191
-
Adaptive evolution of the Myo6 gene in Old World fruit bats (family: Pteropodidae) [serial online]
-
Available at, Accessed October 13, 2013
-
Shen B, Han X, Jones G, Rossiter SJ, Zhang S. Adaptive evolution of the Myo6 gene in Old World fruit bats (family: Pteropodidae) [serial online]. PLoS One. 2013; 8: e62307. Available at: http://www. ncbi. nlm. nih. gov/pmc/articles/PMC3631194/. Accessed October 13, 2013.
-
(2013)
PLoS One
, vol.8
-
-
Shen, B.1
Han, X.2
Jones, G.3
Rossiter, S.J.4
Zhang, S.5
-
33
-
-
84876460957
-
Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction
-
Williams LH, Miller KA, Dahl HH, Manji SS. Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction. Hear Res. 2013; 299: 53-62.
-
(2013)
Hear Res
, vol.299
, pp. 53-62
-
-
Williams, L.H.1
Miller, K.A.2
Dahl, H.H.3
Manji, S.S.4
-
34
-
-
0026737366
-
Immunogold localization of myosin in the photoreceptor cilium
-
Chaitin MH, Coelho N. Immunogold localization of myosin in the photoreceptor cilium. Invest Ophthalmol Vis Sci. 1992; 33: 3103-3108.
-
(1992)
Invest Ophthalmol Vis Sci
, vol.33
, pp. 3103-3108
-
-
Chaitin, M.H.1
Coelho, N.2
-
35
-
-
84887012820
-
Examination of iris, ciliary body and choroid
-
In: New Delhi: Elsevier Health Sciences
-
Mukherjee PK. Examination of iris, ciliary body and choroid. In: Clinical Examination in Ophthalmology. New Delhi: Elsevier Health Sciences; 2007: 141-157.
-
(2007)
Clinical Examination in Ophthalmology
, pp. 141-157
-
-
Mukherjee, P.K.1
-
36
-
-
55949087436
-
Altered visual function in monocarboxylate transporter 3 (Slc16a8) knockout mice
-
Daniele LL, Sauer B, Gallagher SM, Pugh EN Jr, Philp NJ. Altered visual function in monocarboxylate transporter 3 (Slc16a8) knockout mice. Am J Physiol Cell Physiol. 2008; 295: C451-C457.
-
(2008)
Am J Physiol Cell Physiol
, vol.295
-
-
Daniele, L.L.1
Sauer, B.2
Gallagher, S.M.3
Pugh Jr., E.N.4
Philp, N.J.5
-
37
-
-
84867283236
-
Lack of the sodiumdriven chloride bicarbonate exchanger NCBE impairs visual function in the mouse retina [serial online]
-
Available at, Accessed October 13, 2013
-
Hilgen G, Huebner AK, Tanimoto N, et al. Lack of the sodiumdriven chloride bicarbonate exchanger NCBE impairs visual function in the mouse retina [serial online]. PLoS One. 2012; 7: e46155. Available at: http://www. ncbi. nlm. nih. gov/pmc/articles/PMC3467262/. Accessed October 13, 2013.
-
(2012)
PLoS One
, vol.7
-
-
Hilgen, G.1
Huebner, A.K.2
Tanimoto, N.3
-
38
-
-
2442648066
-
Inhibition of the ATPdriven proton pump in RPE lysosomes by the major lipofuscin fluorophore A2-E may contribute to the pathogenesis of agerelated macular degeneration
-
Bergmann M, Schütt F, Holz FG, Kopitz J. Inhibition of the ATPdriven proton pump in RPE lysosomes by the major lipofuscin fluorophore A2-E may contribute to the pathogenesis of agerelated macular degeneration. FASEB J. 2004; 18: 562-564.
-
(2004)
FASEB J
, vol.18
, pp. 562-564
-
-
Bergmann, M.1
Schütt, F.2
Holz, F.G.3
Kopitz, J.4
-
39
-
-
84867103427
-
Autophagy receptors link myosin VI to autophagosomes to mediate Tom1-dependent autophagosome maturation and fusion with the lysosome
-
Tumbarello DA, Waxse BJ, Arden SD, Bright NA, Kendrick-Jones J, Buss F. Autophagy receptors link myosin VI to autophagosomes to mediate Tom1-dependent autophagosome maturation and fusion with the lysosome. Nat Cell Biol. 2012; 14: 1024-1035.
-
(2012)
Nat Cell Biol
, vol.14
, pp. 1024-1035
-
-
Tumbarello, D.A.1
Waxse, B.J.2
Arden, S.D.3
Bright, N.A.4
Kendrick-Jones, J.5
Buss, F.6
-
40
-
-
0036086788
-
Expression of myosin VI within the early endocytic pathway in adult and developing proximal tubules
-
Biemesderfer D, Mentone SA, Mooseker M, Hasson T. Expression of myosin VI within the early endocytic pathway in adult and developing proximal tubules. Am J Physiol Renal Physiol. 2002; 282: F785-F794.
-
(2002)
Am J Physiol Renal Physiol
, vol.282
-
-
Biemesderfer, D.1
Mentone, S.A.2
Mooseker, M.3
Hasson, T.4
-
41
-
-
33947215456
-
Myosin VI targeting to clathrin-coated structures and dimerization is mediated by binding to Disabled-2 and PtdIns(4, 5)P2
-
Spudich G, Chibalina MV, Au JS, Arden SD, Buss F, Kendrick-Jones J. Myosin VI targeting to clathrin-coated structures and dimerization is mediated by binding to Disabled-2 and PtdIns(4, 5)P2. Nat Cell Biol. 2007; 9: 176-183.
-
(2007)
Nat Cell Biol
, vol.9
, pp. 176-183
-
-
Spudich, G.1
Chibalina, M.V.2
Au, J.S.3
Arden, S.D.4
Buss, F.5
Kendrick-Jones, J.6
-
42
-
-
0036242467
-
Myosin VI binds to and localises with Dab2, potentially linking receptor-mediated endocytosis and the actin cytoskeleton
-
Morris SM, Arden SD, Roberts RC, et al. Myosin VI binds to and localises with Dab2, potentially linking receptor-mediated endocytosis and the actin cytoskeleton. Traffic. 2002; 3: 331-341.
-
(2002)
Traffic
, vol.3
, pp. 331-341
-
-
Morris, S.M.1
Arden, S.D.2
Roberts, R.C.3
-
43
-
-
0035898659
-
Myosin VI isoform localized to clathrin-coated vesicles with a role in clathrin-mediated endocytosis
-
Buss F, Arden SD, Lindsay M, Luzio JP, Kendrick-Jones J. Myosin VI isoform localized to clathrin-coated vesicles with a role in clathrin-mediated endocytosis. EMBO J. 2001; 20: 3676-3684.
-
(2001)
EMBO J
, vol.20
, pp. 3676-3684
-
-
Buss, F.1
Arden, S.D.2
Lindsay, M.3
Luzio, J.P.4
Kendrick-Jones, J.5
-
44
-
-
0035941081
-
Myosin VI: New force in clathrin mediated endocytosis
-
Buss F, Luzio JP, Kendrick-Jones J. Myosin VI: new force in clathrin mediated endocytosis. FEBS Lett. 2001; 508: 295-299.
-
(2001)
FEBS Lett
, vol.508
, pp. 295-299
-
-
Buss, F.1
Luzio, J.P.2
Kendrick-Jones, J.3
-
45
-
-
79953718772
-
A high precision survey of the molecular dynamics of mammalian clathrin-mediated endocytosis [serial online]
-
Accessed October 13, 2013
-
Taylor MJ, Perrais D, Merrifield CJ. A high precision survey of the molecular dynamics of mammalian clathrin-mediated endocytosis [serial online]. PLoS Biol. 2011; 9: e1000604. http://www. ncbi. nlm. nih. gov/pmc/articles/PMC3062526/. Accessed October 13, 2013.
-
(2011)
PLoS Biol
, vol.9
-
-
Taylor, M.J.1
Perrais, D.2
Merrifield, C.J.3
-
46
-
-
84869070327
-
Dynamic exchange of myosin VI on endocytic structures
-
Bond LM, Arden SD, Kendrick-Jones J, Buss F, Sellers JR. Dynamic exchange of myosin VI on endocytic structures. J Biol Chem. 2012; 287: 38637-38646.
-
(2012)
J Biol Chem
, vol.287
, pp. 38637-38646
-
-
Bond, L.M.1
Arden, S.D.2
Kendrick-Jones, J.3
Buss, F.4
Sellers, J.R.5
-
47
-
-
77952776082
-
a-AP-2 directs myosin VI-dependent endocytosis of cystic fibrosis transmembrane conductance regulator chloride channels in the intestine
-
Collaco A, Jakab R, Hegan P, Mooseker M, Ameen N. a-AP-2 directs myosin VI-dependent endocytosis of cystic fibrosis transmembrane conductance regulator chloride channels in the intestine. J Biol Chem. 2010; 285: 17177-17187.
-
(2010)
J Biol Chem
, vol.285
, pp. 17177-17187
-
-
Collaco, A.1
Jakab, R.2
Hegan, P.3
Mooseker, M.4
Ameen, N.5
-
48
-
-
4444379442
-
Myosin VI regulates endocytosis of the cystic fibrosis transmembrane conductance regulator
-
Swiatecka-Urban A, Boyd C, Coutermarsh B, et al. Myosin VI regulates endocytosis of the cystic fibrosis transmembrane conductance regulator. J Biol Chem. 2004; 279: 38025-38031.
-
(2004)
J Biol Chem
, vol.279
, pp. 38025-38031
-
-
Swiatecka-Urban, A.1
Boyd, C.2
Coutermarsh, B.3
-
49
-
-
34447549184
-
Defective CFTR apical endocytosis and enterocyte brush border in myosin VI-deficient mice
-
Ameen N, Apodaca G. Defective CFTR apical endocytosis and enterocyte brush border in myosin VI-deficient mice. Traffic. 2007; 8: 998-1006.
-
(2007)
Traffic
, vol.8
, pp. 998-1006
-
-
Ameen, N.1
Apodaca, G.2
-
50
-
-
0032827007
-
A cognitive model of generalized anxiety disorder
-
Wells A. A cognitive model of generalized anxiety disorder. Behav Modif. 1999; 23: 526-555.
-
(1999)
Behav Modif
, vol.23
, pp. 526-555
-
-
Wells, A.1
-
52
-
-
0034739798
-
Genomic structure of the human unconventional myosin VI gene
-
Ahituv N, Sobe T, Robertson NG, Morton CC, Taggart RT, Avraham KB. Genomic structure of the human unconventional myosin VI gene. Gene. 2000; 261: 269-275.
-
(2000)
Gene
, vol.261
, pp. 269-275
-
-
Ahituv, N.1
Sobe, T.2
Robertson, N.G.3
Morton, C.C.4
Taggart, R.T.5
Avraham, K.B.6
-
53
-
-
0023788801
-
Domains, motions and regulation in the myosin head
-
Vibert P, Cohen C. Domains, motions and regulation in the myosin head. J Muscle Res Cell Motil. 1988; 9: 296-305.
-
(1988)
J Muscle Res Cell Motil
, vol.9
, pp. 296-305
-
-
Vibert, P.1
Cohen, C.2
-
54
-
-
0023484279
-
Myosin structure and function in cell motility
-
Warrick HM, Spudich JA. Myosin structure and function in cell motility. Ann Rev Cell Biol. 1987; 3: 379-421.
-
(1987)
Ann Rev Cell Biol
, vol.3
, pp. 379-421
-
-
Warrick, H.M.1
Spudich, J.A.2
-
55
-
-
0028860302
-
A type VII myosin encoded by the mouse deafness gene shaker-1
-
Gibson F, Walsh J, Mburu P, et al. 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
-
56
-
-
0028815440
-
Defective myosin VIIA gene responsible for Usher syndrome type 1B
-
Weil D, Blanchard S, Kaplan J, 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
-
57
-
-
0242509950
-
Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration
-
Libby RT, Kitamoto J, Holme RH, Williams DS, Steel KP. Cdh23 mutations in the mouse are associated with retinal dysfunction but not retinal degeneration. Exp Eye Res. 2003; 77: 731-739.
-
(2003)
Exp Eye Res
, vol.77
, pp. 731-739
-
-
Libby, R.T.1
Kitamoto, J.2
Holme, R.H.3
Williams, D.S.4
Steel, K.P.5
-
58
-
-
0035090360
-
Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B
-
Libby RT, Steel KP. Electroretinographic anomalies in mice with mutations in Myo7a, the gene involved in human Usher syndrome type 1B. Invest Ophthalmol Vis Sci. 2001; 42: 770-778.
-
(2001)
Invest Ophthalmol Vis Sci
, vol.42
, pp. 770-778
-
-
Libby, R.T.1
Steel, K.P.2
-
59
-
-
0346271777
-
Mouse models for Usher syndrome 1B
-
Lillo C, Kitamoto J, Liu X, Quint E, Steel KP, Williams DS. Mouse models for Usher syndrome 1B. Adv Exp Med Biol. 2003; 533: 143-150.
-
(2003)
Adv Exp Med Biol
, vol.533
, pp. 143-150
-
-
Lillo, C.1
Kitamoto, J.2
Liu, X.3
Quint, E.4
Steel, K.P.5
Williams, D.S.6
-
61
-
-
84855170002
-
Retinal disease course in Usher syndrome 1B due to MYO7A mutations
-
Jacobson SG, Cideciyan AV, Gibbs D, et al. Retinal disease course in Usher syndrome 1B due to MYO7A mutations. Invest Ophthalmol Vis Sci. 2011; 52: 7924-7936.
-
(2011)
Invest Ophthalmol Vis Sci
, vol.52
, pp. 7924-7936
-
-
Jacobson, S.G.1
Cideciyan, A.V.2
Gibbs, D.3
-
62
-
-
77449156194
-
Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B
-
Gibbs D, Diemer T, Khanobdee K, Hu J, Bok D, Williams DS. Function of MYO7A in the human RPE and the validity of shaker1 mice as a model for Usher syndrome 1B. Invest Ophthalmol Vis Sci. 2010; 51: 1130-1135.
-
(2010)
Invest Ophthalmol Vis Sci
, vol.51
, pp. 1130-1135
-
-
Gibbs, D.1
Diemer, T.2
Khanobdee, K.3
Hu, J.4
Bok, D.5
Williams, D.S.6
-
63
-
-
80053342176
-
The many different cellular functions of MYO7A in the retina
-
Williams DS, Lopes VS. The many different cellular functions of MYO7A in the retina. Biochem Soc Trans. 2011; 39: 1207-1210.
-
(2011)
Biochem Soc Trans
, vol.39
, pp. 1207-1210
-
-
Williams, D.S.1
Lopes, V.S.2
|