-
1
-
-
0025983772
-
An improved method for isolation and culture of pigment epithelial cells from rat retina
-
Chang, C. W., Roque, R. S., Defoe, D. M., and Caldwell, R. B., 1991, An improved method for isolation and culture of pigment epithelial cells from rat retina. Curr. Eye Res. 10:1081-1086.
-
(1991)
Curr. Eye Res.
, vol.10
, pp. 1081-1086
-
-
Chang, C.W.1
Roque, R.S.2
Defoe, D.M.3
Caldwell, R.B.4
-
2
-
-
0029920657
-
Localization of the human RGR opsin gene to chromosome 10q23
-
Chen, X. N., Korenberg, J. R., Jiang, M., Shen, D., and Fong, H. K., 1996, Localization of the human RGR opsin gene to chromosome 10q23. Hum. Genet. 97:720-722.
-
(1996)
Hum. Genet.
, vol.97
, pp. 720-722
-
-
Chen, X.N.1
Korenberg, J.R.2
Jiang, M.3
Shen, D.4
Fong, H.K.5
-
3
-
-
0022453392
-
Phagocytosis of light- and dark-adapted rod outer segments by cultured RPE cells: A reassessment
-
Colley, N. J., and Hall, M. O., 1986, Phagocytosis of light- and dark-adapted rod outer segments by cultured RPE cells: a reassessment. Exp. Eye Res. 42:323-329.
-
(1986)
Exp. Eye Res.
, vol.42
, pp. 323-329
-
-
Colley, N.J.1
Hall, M.O.2
-
4
-
-
0028903353
-
A human retinal pigment epithelial cell line that retains epithelial characteristics after prolonged culture
-
Davis, A. A., Bernstein, P. S., Bok, D., Turner, J., Nachtigal, M., and Hunt, R. C., 1995, A human retinal pigment epithelial cell line that retains epithelial characteristics after prolonged culture. Invest. Ophthalmol. Vis. Sci. 36:955-964.
-
(1995)
Invest. Ophthalmol. Vis. Sci.
, vol.36
, pp. 955-964
-
-
Davis, A.A.1
Bernstein, P.S.2
Bok, D.3
Turner, J.4
Nachtigal, M.5
Hunt, R.C.6
-
5
-
-
0037053320
-
Mertk triggers uptake of photoreceptor outer segments during phagocytosis by cultured retinal pigment epithelial cells
-
Feng, W., Yasumura, D., Matthes, M. T., LaVail, M. M., and Vollrath, D., 2002, Mertk triggers uptake of photoreceptor outer segments during phagocytosis by cultured retinal pigment epithelial cells. J. Biol. Chem. 277:17016-17022.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 17016-17022
-
-
Feng, W.1
Yasumura, D.2
Matthes, M.T.3
LaVail, M.M.4
Vollrath, D.5
-
6
-
-
0030695436
-
Phagocytosis of rod outer segments by retinal pigment epithelial cells requires alpha(v)beta5 integrin for binding but not for internalization
-
Finnemann, S. C., Bonilha, V. L., Marmorstein, A. D., and Rodriguez-Boulan, E., 1997, Phagocytosis of rod outer segments by retinal pigment epithelial cells requires alpha(v)beta5 integrin for binding but not for internalization. Proc. Natl. Acad. Sci. U S A 94:12932-12937.
-
(1997)
Proc. Natl. Acad. Sci. U S A
, vol.94
, pp. 12932-12937
-
-
Finnemann, S.C.1
Bonilha, V.L.2
Marmorstein, A.D.3
Rodriguez-Boulan, E.4
-
7
-
-
0033757463
-
Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
-
Gal, A., Li, Y., Thompson, D. A., Weir, J., Orth, U., Jacobson, S. G., Apfelstedt-Sylla, E., and Vollrath, D., 2000, Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa. Nat. Genet. 26:270-271.
-
(2000)
Nat. Genet.
, vol.26
, pp. 270-271
-
-
Gal, A.1
Li, Y.2
Thompson, D.A.3
Weir, J.4
Orth, U.5
Jacobson, S.G.6
Apfelstedt-Sylla, E.7
Vollrath, D.8
-
8
-
-
0030593238
-
The gene for PEDF, a retinal growth factor is a prime candidate for retinitis pigmentosa and is tightly linked to the RP13 locus on chromosome 17p13.3
-
Goliath, R., Tombran-Tink, J., Rodriquez, I. R., Chader, G., Ramesar, R., and Greenberg, J., 1996, The gene for PEDF, a retinal growth factor is a prime candidate for retinitis pigmentosa and is tightly linked to the RP13 locus on chromosome 17p13.3. Mol. Vis. 2:5.
-
(1996)
Mol. Vis.
, vol.2
, pp. 5
-
-
Goliath, R.1
Tombran-Tink, J.2
Rodriquez, I.R.3
Chader, G.4
Ramesar, R.5
Greenberg, J.6
-
9
-
-
0031255068
-
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy
-
Gu, S. M., Thompson, D. A., Srikumari, C. R., Lorenz, B., Finckh, U., Nicoletti, A., Murthy, K. R., Rathmann, M., Kumaramanickavel, G., Denton, M. J., and Gal, A., 1997, Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat. Genet. 17:194-197.
-
(1997)
Nat. Genet.
, vol.17
, pp. 194-197
-
-
Gu, S.M.1
Thompson, D.A.2
Srikumari, C.R.3
Lorenz, B.4
Finckh, U.5
Nicoletti, A.6
Murthy, K.R.7
Rathmann, M.8
Kumaramanickavel, G.9
Denton, M.J.10
Gal, A.11
-
10
-
-
0018068531
-
Phagocytosis of light- and dark-adapted rod outer segments by cultured pigment epithelium
-
Hall, M. O., 1978, Phagocytosis of light- and dark-adapted rod outer segments by cultured pigment epithelium. Science 202:526-528.
-
(1978)
Science
, vol.202
, pp. 526-528
-
-
Hall, M.O.1
-
11
-
-
0028787263
-
Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B
-
Hasson, T., Heintzelman, M. B., Santos-Sacchi, J., Corey, D. P., and Mooseker, M. S., 1995, Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B. Proc. Natl. Acad Sci. USA 92:9815-9819.
-
(1995)
Proc. Natl. Acad Sci. USA
, vol.92
, pp. 9815-9819
-
-
Hasson, T.1
Heintzelman, M.B.2
Santos-Sacchi, J.3
Corey, D.P.4
Mooseker, M.S.5
-
12
-
-
0021358277
-
Distribution of microtubules in cultured RPE cells from normal and dystrophic RCS rats
-
Irons, M. J., and Kalnins, V. I., 1984, Distribution of microtubules in cultured RPE cells from normal and dystrophic RCS rats. Invest. Ophthalmol. Vis. Sci. 25:434-439.
-
(1984)
Invest. Ophthalmol. Vis. Sci.
, vol.25
, pp. 434-439
-
-
Irons, M.J.1
Kalnins, V.I.2
-
13
-
-
0032085412
-
Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice
-
Liu, X., Ondek, B., and Williams, D. S., 1998a, Mutant myosin VIIa causes defective melanosome distribution in the RPE of shaker-1 mice. Nat. Genet. 19:117-118.
-
(1998)
Nat. Genet.
, vol.19
, pp. 117-118
-
-
Liu, X.1
Ondek, B.2
Williams, D.S.3
-
14
-
-
0033178341
-
Myosin VIIa participates in opsin transport through the photoreceptor cilium
-
Liu, X., Udovichenko, I. P., Brown, S. D. M., Steel, K. P., and Williams, D. S., 1999, Myosin VIIa participates in opsin transport through the photoreceptor cilium. J. Neurosci. 19:6267-6274.
-
(1999)
J. Neurosci.
, vol.19
, pp. 6267-6274
-
-
Liu, X.1
Udovichenko, I.P.2
Brown, S.D.M.3
Steel, K.P.4
Williams, D.S.5
-
15
-
-
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., Bundey, S., and Brown, S. D., 1998b, Mutations in the myosin VIIA gene cause a wide phenotypic spectrum, including atypical Usher syndrome. 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
Bundey, S.11
Brown, S.D.12
-
16
-
-
0031252434
-
Mutations in RPE65 cause Leber's congenital amaurosis
-
Marlhens, F., Bareil, C., Griffoin, J. M., Zrenner, E., Amalric, P., Eliaou, C., Liu, S. Y., Harris, E., Redmond, T. M., Arnaud, B., Claustres, M., and Hamel, C. P., 1997, Mutations in RPE65 cause Leber's congenital amaurosis. Nat. Genet. 17:139-141.
-
(1997)
Nat. Genet.
, vol.17
, pp. 139-141
-
-
Marlhens, F.1
Bareil, C.2
Griffoin, J.M.3
Zrenner, E.4
Amalric, P.5
Eliaou, C.6
Liu, S.Y.7
Harris, E.8
Redmond, T.M.9
Arnaud, B.10
Claustres, M.11
Hamel, C.P.12
-
17
-
-
0022180810
-
An improved method for isolation and culture of rat retinal pigment epithelial cells
-
Mayerson, P. L., Hall, M. O., Clark, V., and Abrams, T., 1985, An improved method for isolation and culture of rat retinal pigment epithelial cells. Invest. Ophthalmol. Vis. Sci. 26:1599-1609.
-
(1985)
Invest. Ophthalmol. Vis. Sci.
, vol.26
, pp. 1599-1609
-
-
Mayerson, P.L.1
Hall, M.O.2
Clark, V.3
Abrams, T.4
-
18
-
-
0027289136
-
Spontaneously arising immortal cell line of rat retinal pigmented epithelial cells
-
McLaren, M. J., Sasabe, T., Li, C. Y., Brown, M. E., and Inana, G., 1993, Spontaneously arising immortal cell line of rat retinal pigmented epithelial cells. Exp. Cell Res. 204:311-320.
-
(1993)
Exp. Cell Res.
, vol.204
, pp. 311-320
-
-
McLaren, M.J.1
Sasabe, T.2
Li, C.Y.3
Brown, M.E.4
Inana, G.5
-
19
-
-
0032708573
-
Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa
-
Morimura, H., Saindelle-Ribeaudeau, F., Berson, E. L., and Dryja, T. P., 1999, Mutations in RGR, encoding a light-sensitive opsin homologue, in patients with retinitis pigmentosa. Nat. Genet. 23:393-394.
-
(1999)
Nat. Genet.
, vol.23
, pp. 393-394
-
-
Morimura, H.1
Saindelle-Ribeaudeau, F.2
Berson, E.L.3
Dryja, T.P.4
-
20
-
-
0027506111
-
Immortalization of polarized rat retinal pigment epithelium
-
Nabi, I. R., Mathews, A. P., Cohen-Gould, L., Gundersen, D., and Rodriguez-Boulan, E., 1993, Immortalization of polarized rat retinal pigment epithelium. J. Cell Sci. 104:37-49.
-
(1993)
J. Cell Sci.
, vol.104
, pp. 37-49
-
-
Nabi, I.R.1
Mathews, A.P.2
Cohen-Gould, L.3
Gundersen, D.4
Rodriguez-Boulan, E.5
-
21
-
-
0032475826
-
Role for the target enzyme in deactivation of photoreceptor G protein in vivo
-
Tsang, S. H., Burns, M. E., Calvert, P. D., Gouras, P., Baylor, D. A., Goff, S. P., and Arshavsky, V. Y., 1998, Role for the target enzyme in deactivation of photoreceptor G protein in vivo. Science 282:117-121.
-
(1998)
Science
, vol.282
, pp. 117-121
-
-
Tsang, S.H.1
Burns, M.E.2
Calvert, P.D.3
Gouras, P.4
Baylor, D.A.5
Goff, S.P.6
Arshavsky, V.Y.7
-
22
-
-
0035940504
-
Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk
-
Vollrath, D., Feng, W., Duncan, J. L., Yasumura, D., D'Cruz, P. M., Chappelow, A., Matthes, M. T., Kay, M. A., and LaVail, M. M., 2001, Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk. Proc. Natl. Acad. Sci. U S A 98:12584-12589.
-
(2001)
Proc. Natl. Acad. Sci. U S A
, vol.98
, pp. 12584-12589
-
-
Vollrath, D.1
Feng, W.2
Duncan, J.L.3
Yasumura, D.4
D'Cruz, P.M.5
Chappelow, A.6
Matthes, M.T.7
Kay, M.A.8
LaVail, M.M.9
-
23
-
-
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, M. D., Kelley, P. M., Kimberling, W. J., Wagenaar, M., Levi-Acobas, F., Larget-Piet, D., Munnich, A., Steel, K. P., Brown, S. D. M., and Petit, C., 1995, Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 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
Kelley, P.M.11
Kimberling, W.J.12
Wagenaar, M.13
Levi-Acobas, F.14
Larget-Piet, D.15
Munnich, A.16
Steel, K.P.17
Brown, S.D.M.18
Petit, C.19
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