-
1
-
-
0029740113
-
Retinal degeneration in mice lacking the gamma subunit of rod cGMF phosphodiesterase
-
Tsang SH, Gouras P, Yumashita CK, et al. Retinal degeneration in mice lacking the gamma subunit of rod cGMF phosphodiesterase. Science. 1996;272:1026-1029.
-
(1996)
Science
, vol.272
, pp. 1026-1029
-
-
Tsang, S.H.1
Gouras, P.2
Yumashita, C.K.3
-
2
-
-
0032475826
-
Role for the target enzyme in deactivation of photoreceptor g-protein in vivo
-
Tsang SH, Burns ME, Calvert PD, et al. Role for the target enzyme in deactivation of photoreceptor G-protein in vivo. Science. 1998; 282:117-121.
-
(1998)
Science
, vol.282
, pp. 117-121
-
-
Tsang, S.H.1
Burns, M.E.2
Calvert, P.D.3
-
3
-
-
0027248024
-
Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary nightblindness
-
Dryja TP, Berson EL, Rao VR, Oprian DD. Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary nightblindness. Nat Genet. 1993;4:280-283.
-
(1993)
Nat Genet.
, vol.4
, pp. 280-283
-
-
Dryja, T.P.1
Berson, E.L.2
Rao, V.R.3
Oprian, D.D.4
-
4
-
-
0028128535
-
Heterozygous missense mutation in the rod GMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness
-
Gal A, Orth U, Baehr W, et al. Heterozygous missense mutation in the rod GMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness. Nat Genet. 1994;7:64-68.
-
(1994)
Nat Genet.
, vol.7
, pp. 64-68
-
-
Gal, A.1
Orth, U.2
Baehr, W.3
-
5
-
-
0028798659
-
Dark-light model for night blindness from the human rhodopsin Gly-90-Asp mutation
-
Sieving P, Richards JE, Naarendorp F, et al. Dark-light model for night blindness from the human rhodopsin Gly-90-Asp mutation. Proc Natl Acad Sci USA. 1995;92:880-884.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 880-884
-
-
Sieving, P.1
Richards, J.E.2
Naarendorp, F.3
-
6
-
-
0029067542
-
A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese
-
Fuchs S, Nakazawa M, Maw M, et al. A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese. Nat Genet. 1995;10:360-362.
-
(1995)
Nat Genet.
, vol.10
, pp. 360-362
-
-
Fuchs, S.1
Nakazawa, M.2
Maw, M.3
-
7
-
-
0029902034
-
Missense mutation in the gene encoding the alpha unit of rod transducin in the Nougaret form of congenital stationary night blindness
-
Dryja TP, Hahn LB, Beboul T, Armaud B. Missense mutation in the gene encoding the alpha unit of rod transducin in the Nougaret form of congenital stationary night blindness. Nat Genet. 1996;13: 358-360.
-
(1996)
Nat Genet.
, vol.13
, pp. 358-360
-
-
Dryja, T.P.1
Hahn, L.B.2
Beboul, T.3
Armaud, B.4
-
8
-
-
0031038950
-
Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness
-
Yamamoto S, Kimberly C, Berson EL, Dryja TP. Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness. Nat Genet. 1997;15:175-178.
-
(1997)
Nat Genet.
, vol.15
, pp. 175-178
-
-
Yamamoto, S.1
Kimberly, C.2
Berson, E.L.3
Dryja, T.P.4
-
9
-
-
17344366487
-
An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness
-
Strom TM, Nyakatura G, Apfelstedt-Sylla E, et al. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:260-263.
-
(1998)
Nat Genet.
, vol.19
, pp. 260-263
-
-
Strom, T.M.1
Nyakatura, G.2
Apfelstedt-Sylla, E.3
-
10
-
-
0041104621
-
Loss of function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 causes incomplete X-linked congenital stationary night blindness
-
Bech-Hansen NT, Naylor MU, Maybaum TA, et al. Loss of function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 causes incomplete X-linked congenital stationary night blindness. Nat Genet. 1998;19:264-267.
-
(1998)
Nat Genet.
, vol.19
, pp. 264-267
-
-
Bech-Hansen, N.T.1
Naylor, M.U.2
Maybaum, T.A.3
-
11
-
-
0030842611
-
Prolonged photoresponses in transgenic mouse rods lacking arrestin
-
Xu J, Dodd RL, Makino CL, et al. Prolonged photoresponses in transgenic mouse rods lacking arrestin. Nat Genet. 1997;389:505-508.
-
(1997)
Nat Genet.
, vol.389
, pp. 505-508
-
-
Xu, J.1
Dodd, R.L.2
Makino, C.L.3
-
12
-
-
4243775690
-
Arrestin knock-out mice as a model of Oguchi's disease
-
Abstract nr 2993
-
Lyubarsky AL, Pugh EN Jr, Falsini B, et al. Arrestin knock-out mice as a model of Oguchi's disease [ARVO Abstract]. Invest Ophthalmol Vis Sci. 1998;39(4):S643. Abstract nr 2993.
-
(1998)
Invest Ophthalmol Vis Sci.
, vol.39
, Issue.4
-
-
Lyubarsky, A.L.1
Pugh E.N., Jr.2
Falsini, B.3
-
13
-
-
0009473315
-
A potential mouse model of X-linked congenital stationary night blindness
-
Abstract nr 3332
-
Pardue MT, Camille S, Lavail MM, et al. A potential mouse model of X-linked congenital stationary night blindness [ARVO Abstract]. Invest Ophthalmol Vis Sci. 1998;39(4):S725. Abstract nr 3332.
-
(1998)
Invest Ophthalmol Vis Sci.
, vol.39
, Issue.4
-
-
Pardue, M.T.1
Camille, S.2
Lavail, M.M.3
-
14
-
-
0028858741
-
Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene
-
Goto Y, Peachey NS, Ripps H, Naash M. Functional abnormalities in transgenic mice expressing a mutant rhodopsin gene. Invest Ophthalmol Vis Sci. 1995;36:62-71.
-
(1995)
Invest Ophthalmol Vis Sci.
, vol.36
, pp. 62-71
-
-
Goto, Y.1
Peachey, N.S.2
Ripps, H.3
Naash, M.4
-
15
-
-
0026427027
-
Retinal receptors in rodents maximally sensitive to ultraviolet light
-
Jacobs GH, Neitz J, Deegan JF. Retinal receptors in rodents maximally sensitive to ultraviolet light. Nature. 1991;353:655-656.
-
(1991)
Nature
, vol.353
, pp. 655-656
-
-
Jacobs, G.H.1
Neitz, J.2
Deegan, J.F.3
-
16
-
-
0025328952
-
A phosphodiesterase inhibitor specific to a subset of bovine retinal cones
-
Hamilton SE, Hurley JB. A phosphodiesterase inhibitor specific to a subset of bovine retinal cones. J Biol Chem. 1990;265:11259-11264.
-
(1990)
J Biol Chem.
, vol.265
, pp. 11259-11264
-
-
Hamilton, S.E.1
Hurley, J.B.2
-
17
-
-
0027473894
-
Affinities of photoreceptor cGMP phosphodiesterases for rod and cone inhibitory subunits
-
Hamilton SE, Prusti RK, Bentley JK, et al. Affinities of photoreceptor cGMP phosphodiesterases for rod and cone inhibitory subunits. FEBS Lett. 1993;318:157-161.
-
(1993)
FEBS Lett.
, vol.318
, pp. 157-161
-
-
Hamilton, S.E.1
Prusti, R.K.2
Bentley, J.K.3
-
18
-
-
0014020201
-
Das adaptive Verhalten der Mäusenetzhaut
-
Hellner KA. Das adaptive Verhalten der Mäusenetzhaut. Graefes Arch Klin Exp Ophthalmol. 1966;169:166-175.
-
(1966)
Graefes Arch Klin Exp Ophthalmol.
, vol.169
, pp. 166-175
-
-
Hellner, K.A.1
-
19
-
-
0030786395
-
Mechanisms of spectral tuning in the mouse green cone pigment
-
Sun H, Macke JP, Nathans J. Mechanisms of spectral tuning in the mouse green cone pigment. Proc Natl Acad Sci USA. 1997;94: 8860-8865.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 8860-8865
-
-
Sun, H.1
Macke, J.P.2
Nathans, J.3
-
20
-
-
0031789648
-
Rod and cone function in the Nougaret form of stationary night blindness
-
Sandberg MA, Pawlyk BS, Dan J, et al. Rod and cone function in the Nougaret form of stationary night blindness. Arch Ophthalmol. 1998;116:867-872.
-
(1998)
Arch Ophthalmol.
, vol.116
, pp. 867-872
-
-
Sandberg, M.A.1
Pawlyk, B.S.2
Dan, J.3
|