-
1
-
-
0029953583
-
Novel rhodopsin mutation in an autosomal dominant retinitis pigmentosa family: phenotypic variation in both heterozygote and homozygote Val137Met mutant patients
-
Ayuso C., Trujillo M.J., et al. Novel rhodopsin mutation in an autosomal dominant retinitis pigmentosa family: phenotypic variation in both heterozygote and homozygote Val137Met mutant patients. Hum. Genet. 98 1 (1996) 51-54
-
(1996)
Hum. Genet.
, vol.98
, Issue.1
, pp. 51-54
-
-
Ayuso, C.1
Trujillo, M.J.2
-
2
-
-
0024352638
-
Absolute mRNA quantification using the polymerase chain reaction (PCR). A novel approach by a PCR aided transcript titration assay (PATTY)
-
Becker-Andre M., and Hahlbrock K. Absolute mRNA quantification using the polymerase chain reaction (PCR). A novel approach by a PCR aided transcript titration assay (PATTY). Nucleic Acids Res. 17 22 (1989) 9437-9446
-
(1989)
Nucleic Acids Res.
, vol.17
, Issue.22
, pp. 9437-9446
-
-
Becker-Andre, M.1
Hahlbrock, K.2
-
3
-
-
0018823543
-
Population genetic studies of retinitis pigmentosa
-
Boughman J.A., Conneally P.M., et al. Population genetic studies of retinitis pigmentosa. Am. J. Hum. Genet. 32 2 (1980) 223-235
-
(1980)
Am. J. Hum. Genet.
, vol.32
, Issue.2
, pp. 223-235
-
-
Boughman, J.A.1
Conneally, P.M.2
-
4
-
-
2442606621
-
The spectrum of human rhodopsin disease mutations through the lens of interspecific variation
-
Briscoe A.D., Gaur C., et al. The spectrum of human rhodopsin disease mutations through the lens of interspecific variation. Gene 332 (2004) 107-118
-
(2004)
Gene
, vol.332
, pp. 107-118
-
-
Briscoe, A.D.1
Gaur, C.2
-
5
-
-
0021356281
-
Prevalence of retinitis pigmentosa in Maine
-
Bunker C.H., Berson E.L., et al. Prevalence of retinitis pigmentosa in Maine. Am. J. Ophthalmol. 97 3 (1984) 357-365
-
(1984)
Am. J. Ophthalmol.
, vol.97
, Issue.3
, pp. 357-365
-
-
Bunker, C.H.1
Berson, E.L.2
-
6
-
-
0032499711
-
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man
-
Cideciyan A.V., Hood D.C., et al. Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man. Proc. Natl. Acad. Sci. U.S.A. 95 12 (1998) 7103-7108
-
(1998)
Proc. Natl. Acad. Sci. U.S.A.
, vol.95
, Issue.12
, pp. 7103-7108
-
-
Cideciyan, A.V.1
Hood, D.C.2
-
7
-
-
0025105161
-
A point mutation of the rhodopsin gene in one form of retinitis pigmentosa
-
Dryja T.P., McGee T.L., et al. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature 343 6256 (1990) 364-366
-
(1990)
Nature
, vol.343
, Issue.6256
, pp. 364-366
-
-
Dryja, T.P.1
McGee, T.L.2
-
8
-
-
0032033777
-
Rhodopsins from three frog and toad species: sequences and functional comparisons
-
Fyhrquist N., Donner K., et al. Rhodopsins from three frog and toad species: sequences and functional comparisons. Exp. Eye Res. 66 3 (1998) 295-305
-
(1998)
Exp. Eye Res.
, vol.66
, Issue.3
, pp. 295-305
-
-
Fyhrquist, N.1
Donner, K.2
-
9
-
-
0031016243
-
Rhodopsin mutations in inherited retinal dystrophies and dysfunctions
-
Gal A., Apfelstedt-Sylla E., et al. Rhodopsin mutations in inherited retinal dystrophies and dysfunctions. Prog. Retin. Eye Res. 16 (1997) 51-79
-
(1997)
Prog. Retin. Eye Res.
, vol.16
, pp. 51-79
-
-
Gal, A.1
Apfelstedt-Sylla, E.2
-
10
-
-
24144473671
-
Rhodopsin maturation defects induce photoreceptor death by apoptosis: a fly model for RhodopsinPro23His human retinitis pigmentosa
-
Galy A., Roux M.J., et al. Rhodopsin maturation defects induce photoreceptor death by apoptosis: a fly model for RhodopsinPro23His human retinitis pigmentosa. Hum. Mol. Genet. 14 17 (2005) 2547-2557
-
(2005)
Hum. Mol. Genet.
, vol.14
, Issue.17
, pp. 2547-2557
-
-
Galy, A.1
Roux, M.J.2
-
11
-
-
0025967305
-
Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin
-
Heckenlively J.R., Rodriguez J.A., et al. Autosomal dominant sectoral retinitis pigmentosa. Two families with transversion mutation in codon 23 of rhodopsin. Arch. Ophthalmol. 109 1 (1991) 84-91
-
(1991)
Arch. Ophthalmol.
, vol.109
, Issue.1
, pp. 84-91
-
-
Heckenlively, J.R.1
Rodriguez, J.A.2
-
12
-
-
0023884236
-
Clinical findings and common symptoms in retinitis pigmentosa
-
Heckenlively J.R., Yoser S.L., et al. Clinical findings and common symptoms in retinitis pigmentosa. Am. J. Ophthalmol. 105 5 (1988) 504-511
-
(1988)
Am. J. Ophthalmol.
, vol.105
, Issue.5
, pp. 504-511
-
-
Heckenlively, J.R.1
Yoser, S.L.2
-
13
-
-
33748688814
-
Reversal of functional loss in the P23H-3 rat retina by management of ambient light
-
Jozwick C., Valter K., et al. Reversal of functional loss in the P23H-3 rat retina by management of ambient light. Exp. Eye Res. 83 5 (2006) 1074-1080
-
(2006)
Exp. Eye Res.
, vol.83
, Issue.5
, pp. 1074-1080
-
-
Jozwick, C.1
Valter, K.2
-
14
-
-
0026592409
-
Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation
-
Kemp C.M., Jacobson S.G., et al. Abnormal rod dark adaptation in autosomal dominant retinitis pigmentosa with proline-23-histidine rhodopsin mutation. Am. J. Ophthalmol. 113 2 (1992) 165-174
-
(1992)
Am. J. Ophthalmol.
, vol.113
, Issue.2
, pp. 165-174
-
-
Kemp, C.M.1
Jacobson, S.G.2
-
15
-
-
0032548811
-
Transgene expression in Xenopus rods
-
Knox B.E., Schlueter C., et al. Transgene expression in Xenopus rods. FEBS Lett. 423 2 (1998) 117-121
-
(1998)
FEBS Lett.
, vol.423
, Issue.2
, pp. 117-121
-
-
Knox, B.E.1
Schlueter, C.2
-
16
-
-
0029806183
-
Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation
-
Kroll K.L., and Amaya E. Transgenic Xenopus embryos from sperm nuclear transplantations reveal FGF signaling requirements during gastrulation. Development 122 10 (1996) 3173-3183
-
(1996)
Development
, vol.122
, Issue.10
, pp. 3173-3183
-
-
Kroll, K.L.1
Amaya, E.2
-
17
-
-
0031880563
-
Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa
-
Lewin A.S., Drenser K.A., et al. Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa. Nat. Med. 4 8 (1998) 967-971
-
(1998)
Nat. Med.
, vol.4
, Issue.8
, pp. 967-971
-
-
Lewin, A.S.1
Drenser, K.A.2
-
18
-
-
0033827846
-
P23H rhodopsin transgenic rat: correlation of retinal function with histopathology
-
Machida S., Kondo M., et al. P23H rhodopsin transgenic rat: correlation of retinal function with histopathology. Invest. Ophthalmol. Vis. Sci. 41 10 (2000) 3200-3209
-
(2000)
Invest. Ophthalmol. Vis. Sci.
, vol.41
, Issue.10
, pp. 3200-3209
-
-
Machida, S.1
Kondo, M.2
-
19
-
-
0035965360
-
Xenopus rhodopsin promoter. Identification of immediate upstream sequences necessary for high level, rod-specific transcription
-
Mani S.S., Batni S., et al. Xenopus rhodopsin promoter. Identification of immediate upstream sequences necessary for high level, rod-specific transcription. J. Biol. Chem. 276 39 (2001) 36557-36565
-
(2001)
J. Biol. Chem.
, vol.276
, Issue.39
, pp. 36557-36565
-
-
Mani, S.S.1
Batni, S.2
-
20
-
-
0033372525
-
Asymmetric growth and development of the Xenopus laevis retina during metamorphosis is controlled by type III deiodinase
-
Marsh-Armstrong N., Huang H., et al. Asymmetric growth and development of the Xenopus laevis retina during metamorphosis is controlled by type III deiodinase. Neuron 24 4 (1999) 871-878
-
(1999)
Neuron
, vol.24
, Issue.4
, pp. 871-878
-
-
Marsh-Armstrong, N.1
Huang, H.2
-
21
-
-
0024234940
-
Monoclonal antibodies to rhodopsin and other proteins of rod outer segments
-
Molday R.S. Monoclonal antibodies to rhodopsin and other proteins of rod outer segments. Prog. Retin. Eye Res. 8 (1989) 173-209
-
(1989)
Prog. Retin. Eye Res.
, vol.8
, pp. 173-209
-
-
Molday, R.S.1
-
22
-
-
0027251934
-
Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene
-
Naash M.I., Hollyfield J.G., et al. Simulation of human autosomal dominant retinitis pigmentosa in transgenic mice expressing a mutated murine opsin gene. Proc. Natl. Acad. Sci. U.S.A. 90 12 (1993) 5499-5503
-
(1993)
Proc. Natl. Acad. Sci. U.S.A.
, vol.90
, Issue.12
, pp. 5499-5503
-
-
Naash, M.I.1
Hollyfield, J.G.2
-
23
-
-
0029972409
-
Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin
-
Naash M.L., Peachey N.S., et al. Light-induced acceleration of photoreceptor degeneration in transgenic mice expressing mutant rhodopsin. Invest. Ophthalmol. Vis. Sci. 37 5 (1996) 775-782
-
(1996)
Invest. Ophthalmol. Vis. Sci.
, vol.37
, Issue.5
, pp. 775-782
-
-
Naash, M.L.1
Peachey, N.S.2
-
25
-
-
0026463972
-
Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa
-
Olsson J.E., Gordon J.W., et al. Transgenic mice with a rhodopsin mutation (Pro23His): a mouse model of autosomal dominant retinitis pigmentosa. Neuron 9 5 (1992) 815-830
-
(1992)
Neuron
, vol.9
, Issue.5
, pp. 815-830
-
-
Olsson, J.E.1
Gordon, J.W.2
-
26
-
-
0037311463
-
Susceptibility to retinal light damage in transgenic rats with rhodopsin mutations
-
Organisciak D.T., Darrow R.M., et al. Susceptibility to retinal light damage in transgenic rats with rhodopsin mutations. Invest. Ophthalmol. Vis. Sci. 44 2 (2003) 486-492
-
(2003)
Invest. Ophthalmol. Vis. Sci.
, vol.44
, Issue.2
, pp. 486-492
-
-
Organisciak, D.T.1
Darrow, R.M.2
-
27
-
-
0028110523
-
Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene
-
Roof D.J., Adamian M., et al. Rhodopsin accumulation at abnormal sites in retinas of mice with a human P23H rhodopsin transgene. Invest. Ophthalmol. Vis. Sci. 35 12 (1994) 4049-4062
-
(1994)
Invest. Ophthalmol. Vis. Sci.
, vol.35
, Issue.12
, pp. 4049-4062
-
-
Roof, D.J.1
Adamian, M.2
-
28
-
-
0026356244
-
Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene
-
Stone E.M., Kimura A.E., et al. Regional distribution of retinal degeneration in patients with the proline to histidine mutation in codon 23 of the rhodopsin gene. Ophthalmology 98 12 (1991) 1806-1813
-
(1991)
Ophthalmology
, vol.98
, Issue.12
, pp. 1806-1813
-
-
Stone, E.M.1
Kimura, A.E.2
-
29
-
-
0026058548
-
Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa
-
Sung C.H., Schneider B.G., et al. Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa. Proc. Natl. Acad. Sci. U.S.A. 88 19 (1991) 8840-8844
-
(1991)
Proc. Natl. Acad. Sci. U.S.A.
, vol.88
, Issue.19
, pp. 8840-8844
-
-
Sung, C.H.1
Schneider, B.G.2
-
30
-
-
33748100274
-
Characterization of rhodopsin P23H-induced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa
-
Tam B.M., and Moritz O.L. Characterization of rhodopsin P23H-induced retinal degeneration in a Xenopus laevis model of retinitis pigmentosa. Invest. Ophthalmol. Vis. Sci. 47 8 (2006) 3234-3241
-
(2006)
Invest. Ophthalmol. Vis. Sci.
, vol.47
, Issue.8
, pp. 3234-3241
-
-
Tam, B.M.1
Moritz, O.L.2
-
31
-
-
34548169402
-
Dark rearing rescues P23H rhodopsin-induced retinal degeneration in a transgenic Xenopus laevis model of retinitis pigmentosa: a chromophore-dependent mechanism characterized by production of N-terminally truncated mutant rhodopsin
-
Tam B.M., and Moritz O.L. Dark rearing rescues P23H rhodopsin-induced retinal degeneration in a transgenic Xenopus laevis model of retinitis pigmentosa: a chromophore-dependent mechanism characterized by production of N-terminally truncated mutant rhodopsin. J. Neurosci. 27 34 (2007) 9043-9053
-
(2007)
J. Neurosci.
, vol.27
, Issue.34
, pp. 9043-9053
-
-
Tam, B.M.1
Moritz, O.L.2
-
32
-
-
30644475101
-
Mislocalized rhodopsin does not require activation to cause retinal degeneration and neurite outgrowth in Xenopus laevis
-
Tam B.M., Xie G., et al. Mislocalized rhodopsin does not require activation to cause retinal degeneration and neurite outgrowth in Xenopus laevis. J. Neurosci. 26 1 (2006) 203-209
-
(2006)
J. Neurosci.
, vol.26
, Issue.1
, pp. 203-209
-
-
Tam, B.M.1
Xie, G.2
-
33
-
-
0035095225
-
The relationship between opsin overexpression and photoreceptor degeneration
-
Tan E., Wang Q., et al. The relationship between opsin overexpression and photoreceptor degeneration. Invest. Ophthalmol. Vis. Sci. 42 3 (2001) 589-600
-
(2001)
Invest. Ophthalmol. Vis. Sci.
, vol.42
, Issue.3
, pp. 589-600
-
-
Tan, E.1
Wang, Q.2
-
34
-
-
0036327111
-
Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His
-
To K., Adamian M., et al. Histopathologic study of variation in severity of retinitis pigmentosa due to the dominant rhodopsin mutation Pro23His. Am. J. Ophthalmol. 134 2 (2002) 290-293
-
(2002)
Am. J. Ophthalmol.
, vol.134
, Issue.2
, pp. 290-293
-
-
To, K.1
Adamian, M.2
-
35
-
-
0028306459
-
Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate
-
Turner D.L., and Weintraub H. Expression of achaete-scute homolog 3 in Xenopus embryos converts ectodermal cells to a neural fate. Genes Dev. 8 12 (1994) 1434-1447
-
(1994)
Genes Dev.
, vol.8
, Issue.12
, pp. 1434-1447
-
-
Turner, D.L.1
Weintraub, H.2
-
36
-
-
0030808480
-
Expression of a mutant opsin gene increases the susceptibility of the retina to light damage
-
Wang M., Lam T.T., et al. Expression of a mutant opsin gene increases the susceptibility of the retina to light damage. Vis. Neurosci. 14 1 (1997) 55-62
-
(1997)
Vis. Neurosci.
, vol.14
, Issue.1
, pp. 55-62
-
-
Wang, M.1
Lam, T.T.2
-
37
-
-
0037925829
-
Retinitis pigmentosa and allied disorders
-
Ryan S.J., Hinton R., Schachat A.P., and Wilkinson P. (Eds), Elsevier Mosby, Philadelphia
-
Weleber R.G., and Gregory K. Retinitis pigmentosa and allied disorders. In: Ryan S.J., Hinton R., Schachat A.P., and Wilkinson P. (Eds). Retina (2006), Elsevier Mosby, Philadelphia
-
(2006)
Retina
-
-
Weleber, R.G.1
Gregory, K.2
-
38
-
-
0742321905
-
The nature of dominant mutations of rhodopsin and implications for gene therapy
-
Wilson J.H., and Wensel T.G. The nature of dominant mutations of rhodopsin and implications for gene therapy. Mol. Neurobiol. 28 2 (2003) 149-158
-
(2003)
Mol. Neurobiol.
, vol.28
, Issue.2
, pp. 149-158
-
-
Wilson, J.H.1
Wensel, T.G.2
-
39
-
-
0032483063
-
Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa
-
Wu T.H., Ting T.D., et al. Opsin localization and rhodopsin photochemistry in a transgenic mouse model of retinitis pigmentosa. Neuroscience 87 3 (1998) 709-717
-
(1998)
Neuroscience
, vol.87
, Issue.3
, pp. 709-717
-
-
Wu, T.H.1
Ting, T.D.2
|