-
2
-
-
83055187553
-
Mouse model resources for vision research
-
2011:391384
-
Won J, Shi LY, Hicks W, et al. Mouse model resources for vision research. J Ophthalmol. 2011;2011:391384.
-
(2011)
J Ophthalmol
-
-
Won, J.1
Shi, L.Y.2
Hicks, W.3
-
3
-
-
32944473999
-
Gene therapy restores visiondependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis
-
Pang JJ, Chang B, Kumar A, et al. Gene therapy restores visiondependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis. Mol Ther. 2006;13:565-572.
-
(2006)
Mol Ther
, vol.13
, pp. 565-572
-
-
Pang, J.J.1
Chang, B.2
Kumar, A.3
-
4
-
-
34249987381
-
Restoration of cone vision in a mouse model of achromatopsia
-
Alexander JJ, Umino Y, Everhart D, et al. Restoration of cone vision in a mouse model of achromatopsia. Nat Med. 2007;13: 685-687.
-
(2007)
Nat Med
, vol.13
, pp. 685-687
-
-
Alexander, J.J.1
Umino, Y.2
Everhart, D.3
-
5
-
-
0000087516
-
The inheritance of a retinal abnormality in white mice
-
Keeler C. The inheritance of a retinal abnormality in white mice. Proc Natl Acad Sci U S A. 1924;10:329-350.
-
(1924)
Proc Natl Acad Sci U S A
, vol.10
, pp. 329-350
-
-
Keeler, C.1
-
6
-
-
0013893075
-
Retinal degeneration in the mouse is rodless retina
-
Keeler C. Retinal degeneration in the mouse is rodless retina. J Hered. 1966;57:47-50.
-
(1966)
J Hered
, vol.57
, pp. 47-50
-
-
Keeler, C.1
-
7
-
-
0027363757
-
PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect
-
Pittler SJ, Keeler C., Sidman RL, Baehr W. PCR analysis of DNA from 70-year-old sections of rodless retina demonstrates identity with the mouse rd defect. Proc Natl Acad Sci U S A. 1993;90:9616-9619.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 9616-9619
-
-
Pittler, S.J.1
Keeler, C.2
Sidman, R.L.3
Baehr, W.4
-
8
-
-
0018174467
-
A new H-2-linked mutation, rds, causing retinal degeneration in the mouse
-
van Nie R, Ivanyi D, Demant P. A new H-2-linked mutation, rds, causing retinal degeneration in the mouse. Tissue Antigens. 1978;12:106-108.
-
(1978)
Tissue Antigens
, vol.12
, pp. 106-108
-
-
van Nie, R.1
Ivanyi, D.2
Demant, P.3
-
10
-
-
0036181472
-
Retinal degeneration mutants in the mouse
-
Chang B, Hawes NL, Hurd RE, Davisson MT, Nusinowitz S, Heckenlively JR. Retinal degeneration mutants in the mouse. Vision Res. 2002;42:517-525.
-
(2002)
Vision Res
, vol.42
, pp. 517-525
-
-
Chang, B.1
Hawes, N.L.2
Hurd, R.E.3
Davisson, M.T.4
Nusinowitz, S.5
Heckenlively, J.R.6
-
11
-
-
84880725319
-
Retinal Degenerations: Biology, Diagnostics, and Therapeutics
-
Mouse models of RP. In: Tombran-Tink J, Barnstable C, eds, New York, NY
-
Chang B, Hawes N, Davisson M, Heckenlively J. Mouse models of RP. In: Tombran-Tink J, Barnstable C, eds. Retinal Degenerations: Biology, Diagnostics, and Therapeutics. New York, NY: The Humana Press, Inc.; 2007:149-164.
-
(2007)
The Humana Press, Inc
, pp. 149-164
-
-
Chang, B.1
Hawes, N.2
Davisson, M.3
Heckenlively, J.4
-
12
-
-
0027500565
-
Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase
-
Bowes C, Li T, Frankel WN, et al. Localization of a retroviral element within the rd gene coding for the beta subunit of cGMP phosphodiesterase. Proc Natl Acad Sci U S A. 1993;90: 2955-2959.
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 2955-2959
-
-
Bowes, C.1
Li, T.2
Frankel, W.N.3
-
13
-
-
84863723643
-
The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/ 6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes
-
Mattapallil MJ, Wawrousek EF, Chan CC, et al. The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/ 6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes. Invest Ophthalmol Vis Sci. 2012; 53:2921-2927.
-
(2012)
Invest Ophthalmol Vis Sci
, vol.53
, pp. 2921-2927
-
-
Mattapallil, M.J.1
Wawrousek, E.F.2
Chan, C.C.3
-
14
-
-
34247146385
-
Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2
-
Chang B, Dacey MS, Hawes NL, et al. Cone photoreceptor function loss-3, a novel mouse model of achromatopsia due to a mutation in Gnat2. Invest Ophthalmol Vis Sci. 2006;47: 5017-5021.
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 5017-5021
-
-
Chang, B.1
Dacey, M.S.2
Hawes, N.L.3
-
15
-
-
73349130033
-
A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene
-
Chang B, Grau T, Dangel S, et al. A homologous genetic basis of the murine cpfl1 mutant and human achromatopsia linked to mutations in the PDE6C gene. Proc Natl Acad Sci U S A. 2009;106:19581-19586.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 19581-19586
-
-
Chang, B.1
Grau, T.2
Dangel, S.3
-
16
-
-
33644872908
-
The nob2 mouse, a null mutation in Cacna1f: Anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses
-
Chang B, Heckenlively J., Bayley PR, et al. The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses. Vis Neurosci. 2006;23:11-24.
-
(2006)
Vis Neurosci
, vol.23
, pp. 11-24
-
-
Chang, B.1
Heckenlively, J.2
Bayley, P.R.3
-
17
-
-
51849116871
-
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses
-
Maddox DM, Vessey KA, Yarbrough GL, et al. Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responses. J Physiol. 2008;586:4409-4424.
-
(2008)
J Physiol
, vol.586
, pp. 4409-4424
-
-
Maddox, D.M.1
Vessey, K.A.2
Yarbrough, G.L.3
-
18
-
-
85057473970
-
Electrophysiological testing of the mouse visual system
-
Boca Raton, FL, CRC Press
-
Nusinowitz S, Ridder WH III, Heckenlively JR. Electrophysiological testing of the mouse visual system. In: Smith RS, ed. Systematic Evaluation of the Mouse Eye: Anatomy, Pathology, and Biomethods. Boca Raton, FL: CRC Press; 2002:320- 344.
-
(2002)
Systematic Evaluation of the Mouse Eye: Anatomy, Pathology, and Biomethods
, pp. 320
-
-
Nusinowitz, S.1
Ridder, W.H.2
Heckenlively, J.R.3
-
19
-
-
0033922371
-
Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT)
-
Truett GE, Heeger P, Mynatt RL, Truett AA, Walker JA, Warman ML. Preparation of PCR-quality mouse genomic DNA with hot sodium hydroxide and tris (HotSHOT). Biotechniques. 2000; 29:52-54.
-
(2000)
Biotechniques
, vol.29
, pp. 52-54
-
-
Truett, G.E.1
Heeger, P.2
Mynatt, R.L.3
Truett, A.A.4
Walker, J.A.5
Warman, M.L.6
-
20
-
-
0037379831
-
Photoreceptor degeneration and rd1 mutation in grizzled/ mocha mouse strain
-
Qiao X, Pennesi M, Seong E, Gao H, Burmeister M, Wu SM. Photoreceptor degeneration and rd1 mutation in grizzled/ mocha mouse strain. Vision Res. 2003;43:859-865.
-
(2003)
Vision Res
, vol.43
, pp. 859-865
-
-
Qiao, X.1
Pennesi, M.2
Seong, E.3
Gao, H.4
Burmeister, M.5
Wu, S.M.6
-
21
-
-
0035065567
-
A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation (Pdeb(rd1)) in FVB/N-derived transgenic mice
-
Giménez E, Montoliu L. A simple polymerase chain reaction assay for genotyping the retinal degeneration mutation (Pdeb(rd1)) in FVB/N-derived transgenic mice. Lab Anim. 2001;35:153-156.
-
(2001)
Lab Anim
, vol.35
, pp. 153-156
-
-
Giménez, E.1
Montoliu, L.2
-
22
-
-
10744224972
-
CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina
-
Mehalow AK, Kameya S, Smith RS, et al. CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina. Hum Mol Genet. 2003;12:2179-2189.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2179-2189
-
-
Mehalow, A.K.1
Kameya, S.2
Smith, R.S.3
-
23
-
-
74549181020
-
Animal models for retinal degeneration
-
Pang I, Clark AF, ed
-
Samardzija M, Neuhauss SCF, Joly S, Kurz-Levin M, Grimm C. Animal models for retinal degeneration. In: Pang I, Clark AF, ed. Animal Models for Retinal Diseases. New York, NY: The Humana Press, Inc.; 2010:51-79.
-
(2010)
Animal Models For Retinal Diseases. New York, NY: The Humana Press, Inc
, pp. 51-79
-
-
Samardzija, M.1
Neuhauss, S.C.F.2
Joly, S.3
Kurz-Levin, M.4
Grimm, C.5
-
24
-
-
57649185427
-
New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene
-
Sakamoto K, McCluskey M, Wensel TG, Naggert JK, Nishina PM. New mouse models for recessive retinitis pigmentosa caused by mutations in the Pde6a gene. Hum Mol Genet. 2009;18:178-192.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 178-192
-
-
Sakamoto, K.1
McCluskey, M.2
Wensel, T.G.3
Naggert, J.K.4
Nishina, P.M.5
-
25
-
-
0033978890
-
Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene
-
Ikeda S, Shiva N, Ikeda A, et al. Retinal degeneration but not obesity is observed in null mutants of the tubby-like protein 1 gene. Hum Mol Genet. 2000;9:155-163.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 155-163
-
-
Ikeda, S.1
Shiva, N.2
Ikeda, A.3
|