-
1
-
-
0033860406
-
A mouse model of galactose-induced cataracts
-
Ai Y., Zheng Z., O'Brien-Jenkins A., Bernard D. J., Wynshaw-Boris T., Ning C. et al. 2000 A mouse model of galactose-induced cataracts. Hum. Mol. Genet. 9, 1821-1827.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1821-1827
-
-
Ai, Y.1
Zheng, Z.2
O'Brien-Jenkins, A.3
Bernard, D.J.4
Wynshaw-Boris, T.5
Ning, C.6
-
2
-
-
0032780886
-
Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin
-
Berry V., Mackay D., Khaliq S., Francis P. J., Hameed A., Anwar K. et al. 1999 Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin. Hum. Genet. 105, 168-170.
-
(1999)
Hum. Genet.
, vol.105
, pp. 168-170
-
-
Berry, V.1
Mackay, D.2
Khaliq, S.3
Francis, P.J.4
Hameed, A.5
Anwar, K.6
-
3
-
-
33751542492
-
Connexin43 is required for production of the aqueous humor in the murine eye
-
Calera M. R., Topley H. L., Liao Y., Duling B. R., Paul D. L. and Goodenough D. A. 2006 Connexin43 is required for production of the aqueous humor in the murine eye. J. Cell Sci. 119, 4510-4519.
-
(2006)
J. Cell Sci.
, vol.119
, pp. 4510-4519
-
-
Calera, M.R.1
Topley, H.L.2
Liao, Y.3
Duling, B.R.4
Paul, D.L.5
Goodenough, D.A.6
-
4
-
-
33947237989
-
Identification of a missense mutation in the alphaA- crystallin gene of the lop18 mouse
-
Chang B., Hawes N. L., Roderick T. H., Smith R. S., Heckenlively J. R., Horwitz J. and Davisson M. T. 1999 Identification of a missense mutation in the alphaA- crystallin gene of the lop18 mouse. Mol. Vis. 5, 21.
-
(1999)
Mol. Vis.
, vol.5
, pp. 21
-
-
Chang, B.1
Hawes, N.L.2
Roderick, T.H.3
Smith, R.S.4
Heckenlively, J.R.5
Horwitz, J.6
Davisson, M.T.7
-
5
-
-
0036501610
-
A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice
-
Chang B., Wang X., Hawes N. L., Ojakian R., Davisson M. T., Lo W. K. and Gong X. 2002 A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice. Hum. Mol. Genet. 11, 507-513.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 507-513
-
-
Chang, B.1
Wang, X.2
Hawes, N.L.3
Ojakian, R.4
Davisson, M.T.5
Lo, W.K.6
Gong, X.7
-
6
-
-
0030802170
-
Epidemiology of cataract in childhood: a global perspective
-
Foster A., Gilbert C. and Rahi J. 1997 Epidemiology of cataract in childhood: a global perspective. J. Cataract Refract. Surg. 23, suppl 1, 601-604.
-
(1997)
J. Cataract Refract. Surg.
, vol.23
, Issue.SUPPL. 1
, pp. 601-604
-
-
Foster, A.1
Gilbert, C.2
Rahi, J.3
-
7
-
-
8544223794
-
Lens rupture; a new recessive gene in the house mouse
-
Fraser F. C. and Herer M. L. 1948 Lens rupture; a new recessive gene in the house mouse. J. Hered. 39, 149.
-
(1948)
J. Hered.
, vol.39
, pp. 149
-
-
Fraser, F.C.1
Herer, M.L.2
-
8
-
-
55749096082
-
Twenty years of childhood blindness: what have we learnt?
-
Gilbert C. and Muhit M. 2008 Twenty years of childhood blindness: what have we learnt? Community Eye Health21, 46-47.
-
(2008)
Community Eye Health
, vol.21
, pp. 46-47
-
-
Gilbert, C.1
Muhit, M.2
-
9
-
-
11144298645
-
Congenital hereditary cataracts
-
Graw J. 2004 Congenital hereditary cataracts. Int. J. Dev. Biol. 48, 1031-1044.
-
(2004)
Int. J. Dev. Biol.
, vol.48
, pp. 1031-1044
-
-
Graw, J.1
-
10
-
-
0036137847
-
A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse
-
Graw J., Neuhauser-Klaus A., Loster J. and Favor J. 2002 A 6-bp deletion in the Crygc gene leading to a nuclear and radial cataract in the mouse. Invest. Ophthalmol. Vis. Sci. 43, 236-240.
-
(2002)
Invest. Ophthalmol. Vis. Sci.
, vol.43
, pp. 236-240
-
-
Graw, J.1
Neuhauser-Klaus, A.2
Loster, J.3
Favor, J.4
-
11
-
-
68249120153
-
EPHA2 is associated with age-related cortical cataract in mice and humans
-
Jun G., Guo H., Klein B. E., Klein R., Wang J. J., Mitchell P. et al. 2009 EPHA2 is associated with age-related cortical cataract in mice and humans. PLoS Genet. 5, e1000584.
-
(2009)
PLoS Genet.
, vol.5
-
-
Jun, G.1
Guo, H.2
Klein, B.E.3
Klein, R.4
Wang, J.J.5
Mitchell, P.6
-
12
-
-
3042696951
-
Dense cataract and microphthalmia-new spontaneous mutation in BALB/c mice
-
Kohale K., Ingle A., Kelkar A. and Parab P. 2004 Dense cataract and microphthalmia-new spontaneous mutation in BALB/c mice. Comp. Med. 54, 275-279.
-
(2004)
Comp. Med.
, vol.54
, pp. 275-279
-
-
Kohale, K.1
Ingle, A.2
Kelkar, A.3
Parab, P.4
-
13
-
-
0014519324
-
Abnormal development of eyes in mice homozygous for the fidget gene
-
Konyukhov B. V. and Vakhrusheva M. P. 1969 Abnormal development of eyes in mice homozygous for the fidget gene. Teratology2, 147-157.
-
(1969)
Teratology
, vol.2
, pp. 147-157
-
-
Konyukhov, B.V.1
Vakhrusheva, M.P.2
-
14
-
-
57349192021
-
Quantitative trait loci affecting phenotypic variation in the vacuolated lens mouse mutant, a multigenic mouse model of neural tube defects
-
Korstanje R., Desai J., Lazar G., King B., Rollins J., Spurr M. et al. 2008 Quantitative trait loci affecting phenotypic variation in the vacuolated lens mouse mutant, a multigenic mouse model of neural tube defects. Physiol. Genomics35, 296-304.
-
(2008)
Physiol. Genomics
, vol.35
, pp. 296-304
-
-
Korstanje, R.1
Desai, J.2
Lazar, G.3
King, B.4
Rollins, J.5
Spurr, M.6
-
15
-
-
0030028301
-
The gap junction communication channel
-
Kumar N. M. and Gilula N. B. 1996 The gap junction communication channel. Cell84, 381-388.
-
(1996)
Cell
, vol.84
, pp. 381-388
-
-
Kumar, N.M.1
Gilula, N.B.2
-
16
-
-
0035990077
-
Naphthoquinone cataract in mice: mitochondrial change and protection by superoxide dismutase
-
Martynkina L. P., Qian W. and Shichi H. 2002 Naphthoquinone cataract in mice: mitochondrial change and protection by superoxide dismutase. J. Ocul. Pharmacol. Ther. 18, 231-239.
-
(2002)
J. Ocul. Pharmacol. Ther.
, vol.18
, pp. 231-239
-
-
Martynkina, L.P.1
Qian, W.2
Shichi, H.3
-
17
-
-
78349234338
-
-
The National Advisory Eye Council Vision Research, NIH publication No. 87-2755, Bethesda, USA: National Institute of Health
-
The National Advisory Eye Council Vision Research 1987 A National Plan 1987 Evaluation and Update, National Institute of Health, Bethesda, USA, (NIH publication No. 87-2755).
-
(1987)
A National Plan 1987 Evaluation and Update
-
-
-
18
-
-
70350243052
-
Connexins, cell motility, and the cytoskeleton
-
Olk S., Zoidl G. and Dermietzel R. 2009 Connexins, cell motility, and the cytoskeleton. Cell Motil. Cytoskeleton66, 1000-1016.
-
(2009)
Cell Motil. Cytoskeleton
, vol.66
, pp. 1000-1016
-
-
Olk, S.1
Zoidl, G.2
Dermietzel, R.3
-
19
-
-
66849136796
-
Enhanced diabetes-induced cataract in copper-zinc superoxide dismutasenull mice
-
Olofsson E. M., Marklund S. L. and Behndig A. 2009 Enhanced diabetes-induced cataract in copper-zinc superoxide dismutasenull mice. Invest. Ophthalmol. Vis. Sci. 50, 2913-2918.
-
(2009)
Invest. Ophthalmol. Vis. Sci.
, vol.50
, pp. 2913-2918
-
-
Olofsson, E.M.1
Marklund, S.L.2
Behndig, A.3
-
20
-
-
0026352039
-
Connexin46, a novel lens gap junction protein, induces voltage-gated currents in nonjunctional plasma membrane of Xenopus oocytes
-
Paul D. L., Ebihara L., Takemoto L. J., Swenson K. I. and Goodenough D. A. 1991 Connexin46, a novel lens gap junction protein, induces voltage-gated currents in nonjunctional plasma membrane of Xenopus oocytes. J. Cell Biol. 115, 1077-1089.
-
(1991)
J. Cell Biol.
, vol.115
, pp. 1077-1089
-
-
Paul, D.L.1
Ebihara, L.2
Takemoto, L.J.3
Swenson, K.I.4
Goodenough, D.A.5
-
21
-
-
0036023359
-
Disruption of Gja8 (alpha8 connexin) in mice leads to microphthalmia associated with retardation of lens growth and lens fiber maturation
-
Rong P., Wang X., Niesman I., Wu Y., Benedetti L. E., Dunia I. et al. 2002 Disruption of Gja8 (alpha8 connexin) in mice leads to microphthalmia associated with retardation of lens growth and lens fiber maturation. Development129, 167-174.
-
(2002)
Development
, vol.129
, pp. 167-174
-
-
Rong, P.1
Wang, X.2
Niesman, I.3
Wu, Y.4
Benedetti, L.E.5
Dunia, I.6
-
22
-
-
0026727930
-
Autosomal dominant mouse cataract (Lop-10). Consistent differences of expression in heterozygotes
-
Runge P. E., Hawes N. L., Heckenlively J. R., Langley S. H. and Roderick T. H. 1992 Autosomal dominant mouse cataract (Lop-10). Consistent differences of expression in heterozygotes. Invest. Ophthalmol. Vis. Sci. 33, 3202-3208.
-
(1992)
Invest. Ophthalmol. Vis. Sci.
, vol.33
, pp. 3202-3208
-
-
Runge, P.E.1
Hawes, N.L.2
Heckenlively, J.R.3
Langley, S.H.4
Roderick, T.H.5
-
23
-
-
17344390158
-
Plasma membrane channels formed by connexins: their regulation and functions
-
Saez J. C., Berthoud V. M., Branes M. C., Martinez A. D. and Beyer E. C. 2003 Plasma membrane channels formed by connexins: their regulation and functions. Physiol Rev. 83, 1359-1400.
-
(2003)
Physiol Rev.
, vol.83
, pp. 1359-1400
-
-
Saez, J.C.1
Berthoud, V.M.2
Branes, M.C.3
Martinez, A.D.4
Beyer, E.C.5
-
24
-
-
0022897223
-
Map position of dysgenetic lens (dyl) locus on chromosome 4 in the mouse
-
Sanyal S., van Nie R., De Moes J. and Hawkins R. K. 1986 Map position of dysgenetic lens (dyl) locus on chromosome 4 in the mouse. Genet. Res. 48, 199-200.
-
(1986)
Genet. Res.
, vol.48
, pp. 199-200
-
-
Sanyal, S.1
van Nie, R.2
de Moes, J.3
Hawkins, R.K.4
-
25
-
-
0034143650
-
Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract
-
Smith R. S., Hawes N. L., Chang B., Roderick T. H., Akeson E. C. and Heckenlively J. R. 2000 Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract. Genomics63, 314-320.
-
(2000)
Genomics
, vol.63
, pp. 314-320
-
-
Smith, R.S.1
Hawes, N.L.2
Chang, B.3
Roderick, T.H.4
Akeson, E.C.5
Heckenlively, J.R.6
-
26
-
-
0026529805
-
Genetic localization of Hao-1, blind-sterile (bs), and Emv-13 on mouse chromosome 2
-
Spence S. E., Gilbert, D. J., Harris B. S., Davisson M. T., Copeland N. G. and Jenkins N. A. 1992 Genetic localization of Hao-1, blind-sterile (bs), and Emv-13 on mouse chromosome 2. Genomics12, 403-404.
-
(1992)
Genomics
, vol.12
, pp. 403-404
-
-
Spence, S.E.1
Gilbert, D.J.2
Harris, B.S.3
Davisson, M.T.4
Copeland, N.G.5
Jenkins, N.A.6
-
27
-
-
33744911966
-
Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice
-
Talamas E., Jackson L., Koeberl M., Jackson T., McElwee J. L., Hawes N. L. et al. 2006 Early transposable element insertion in intron 9 of the Hsf4 gene results in autosomal recessive cataracts in lop11 and ldis1 mice. Genomics88, 44-51.
-
(2006)
Genomics
, vol.88
, pp. 44-51
-
-
Talamas, E.1
Jackson, L.2
Koeberl, M.3
Jackson, T.4
McElwee, J.L.5
Hawes, N.L.6
-
28
-
-
39549088084
-
A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin
-
Vanita V., Singh J. R., Singh D., Varon R. and Sperling K. 2008 A novel mutation in GJA8 associated with jellyfish-like cataract in a family of Indian origin. Mol. Vis. 14, 323-326.
-
(2008)
Mol. Vis.
, vol.14
, pp. 323-326
-
-
Vanita, V.1
Singh, J.R.2
Singh, D.3
Varon, R.4
Sperling, K.5
-
29
-
-
52449116005
-
UV-B-induced damage to the lens in vitro: prevention by caffeine
-
Varma S. D., Hegde K. R. and Kovtun S. 2008 UV-B-induced damage to the lens in vitro: prevention by caffeine. J. Ocul. Pharmacol. Ther. 24, 439-444.
-
(2008)
J. Ocul. Pharmacol. Ther.
, vol.24
, pp. 439-444
-
-
Varma, S.D.1
Hegde, K.R.2
Kovtun, S.3
-
30
-
-
3042809348
-
Nuclear cataract (nuc)
-
Varnum D. 1981 Nuclear cataract (nuc). Mouse Newslett. 64, 59.
-
(1981)
Mouse Newslett.
, vol.64
, pp. 59
-
-
Varnum, D.1
-
31
-
-
0035789140
-
Characterization of Corn1 mice: Alteration of epithelial and stromal cell gene expression
-
Wang I., Kao C. W., Liu C., Saika S., Nishina P. M., Sundberg J. P. et al. 2001 Characterization of Corn1 mice: Alteration of epithelial and stromal cell gene expression. Mol. Vis. 7, 20-26.
-
(2001)
Mol. Vis.
, vol.7
, pp. 20-26
-
-
Wang, I.1
Kao, C.W.2
Liu, C.3
Saika, S.4
Nishina, P.M.5
Sundberg, J.P.6
-
32
-
-
0027070644
-
Mouse Cx50, a functional member of the connexin family of gap junction proteins, is the lens fiber protein MP70
-
White T. W., Bruzzone R., Goodenough D. A. and Paul D. L. 1992 Mouse Cx50, a functional member of the connexin family of gap junction proteins, is the lens fiber protein MP70. Mol. Biol. Cell3, 711-720.
-
(1992)
Mol. Biol. Cell
, vol.3
, pp. 711-720
-
-
White, T.W.1
Bruzzone, R.2
Goodenough, D.A.3
Paul, D.L.4
-
33
-
-
0032476578
-
Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts
-
White T. W., Goodenough D. A. and Paul D. L. 1998 Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts. J. Cell Biol. 143, 815-825.
-
(1998)
J. Cell Biol.
, vol.143
, pp. 815-825
-
-
White, T.W.1
Goodenough, D.A.2
Paul, D.L.3
-
34
-
-
0036290184
-
Aetiology of congenital and paediatric cataract in an Australian population
-
Wirth M. G., Russell-Eggitt I. M., Craig J. E., Elder J. E. and Mackey D. A. 2002 Aetiology of congenital and paediatric cataract in an Australian population. Br. J. Ophthalmol. 86, 782-786.
-
(2002)
Br. J. Ophthalmol.
, vol.86
, pp. 782-786
-
-
Wirth, M.G.1
Russell-Eggitt, I.M.2
Craig, J.E.3
Elder, J.E.4
Mackey, D.A.5
-
35
-
-
0345517256
-
Characterization of a mouse Cx50 mutation associated with the No2 mouse cataract
-
Xu X. and Ebihara L. 1999 Characterization of a mouse Cx50 mutation associated with the No2 mouse cataract. Invest Ophthalmol. Vis. Sci. 40, 1844-1850.
-
(1999)
Invest Ophthalmol. Vis. Sci.
, vol.40
, pp. 1844-1850
-
-
Xu, X.1
Ebihara, L.2
-
36
-
-
40649092855
-
A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract
-
Yan M., Xiong C., Ye S. Q., Chen Y., Ke M., Zheng F. and Zhou X. 2008 A novel connexin 50 (GJA8) mutation in a Chinese family with a dominant congenital pulverulent nuclear cataract. Mol. Vis. 14, 418-424.
-
(2008)
Mol. Vis.
, vol.14
, pp. 418-424
-
-
Yan, M.1
Xiong, C.2
Ye, S.Q.3
Chen, Y.4
Ke, M.5
Zheng, F.6
Zhou, X.7
|