-
1
-
-
0032792185
-
Clinical and genetic heterogeneity in autosomal dominant cataract
-
Ionides A, Francis P, Berry V, et al. Clinical and genetic heterogeneity in autosomal dominant cataract. Br J Ophthalmol. 1999;83: 802-808.
-
(1999)
Br J Ophthalmol
, vol.83
, pp. 802-808
-
-
Ionides, A.1
Francis, P.2
Berry, V.3
-
2
-
-
0029929286
-
Genetic aspects of embryonic eye development in vertebrates
-
Graw J. Genetic aspects of embryonic eye development in vertebrates. Dev Genet. 1996;18:181-197.
-
(1996)
Dev Genet
, vol.18
, pp. 181-197
-
-
Graw, J.1
-
3
-
-
0030731478
-
Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16
-
Sidjanin DJ, Grimes PA, Pretsch W, et al. Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16. Invest Ophthalmol Vis Sci. 1997;38:2502-2507.
-
(1997)
Invest Ophthalmol Vis Sci
, vol.38
, pp. 2502-2507
-
-
Sidjanin, D.J.1
Grimes, P.A.2
Pretsch, W.3
-
4
-
-
0032815059
-
Mouse models of congenital cataract
-
Graw J. Mouse models of congenital cataract. Eye. 1999;13:438-444.
-
(1999)
Eye
, vol.13
, pp. 438-444
-
-
Graw, J.1
-
5
-
-
0034060264
-
Congenital cataracts: Gene mapping
-
He W, Li S. Congenital cataracts: gene mapping. Hum Genet. 2000; 106:1-13.
-
(2000)
Hum Genet
, vol.106
, pp. 1-13
-
-
He, W.1
Li, S.2
-
6
-
-
0035103149
-
Genetic analysis of cataract in Ihara epileptic rat
-
Yokoyama M, Amano S, Tsuji A, et al. Genetic analysis of cataract in Ihara epileptic rat. Mamm Genome. 2001;12:207-211.
-
(2001)
Mamm Genome
, vol.12
, pp. 207-211
-
-
Yokoyama, M.1
Amano, S.2
Tsuji, A.3
-
7
-
-
0027368678
-
The UPL rat: A new model for hereditary cataracts with two cataract formation types
-
Tomohiro M, Maruyama Y, Yazawa K, Shinzawa S, Mizuno A. The UPL rat: a new model for hereditary cataracts with two cataract formation types. Exp Eye Res. 1993;57:507-510.
-
(1993)
Exp Eye Res
, vol.57
, pp. 507-510
-
-
Tomohiro, M.1
Maruyama, Y.2
Yazawa, K.3
Shinzawa, S.4
Mizuno, A.5
-
8
-
-
0029880456
-
Lens development and crystallin distribution of the early onset hereditary cataract in the UPL rat
-
Tomohiro M, Murata S, Yazawa K, et al. Lens development and crystallin distribution of the early onset hereditary cataract in the UPL rat. Jpn J Ophthalmol. 1996;40:42-52.
-
(1996)
Jpn J Ophthalmol
, vol.40
, pp. 42-52
-
-
Tomohiro, M.1
Murata, S.2
Yazawa, K.3
-
10
-
-
0030837684
-
Immunohistochemical study of calpain-mediated alpha-crystallin proteolysis in the UPL rat hereditary cataract
-
Tomohiro M, Aida Y, Inomata M, et al. Immunohistochemical study of calpain-mediated alpha-crystallin proteolysis in the UPL rat hereditary cataract. Jpn J Ophthalmol. 1997;41:121-129.
-
(1997)
Jpn J Ophthalmol
, vol.41
, pp. 121-129
-
-
Tomohiro, M.1
Aida, Y.2
Inomata, M.3
-
11
-
-
0033777784
-
Construction of a high-throughput rat genetic mapping system with 466 arbitrarily primed-representational difference analysis markers
-
Yamashita S, Yoshida Y, Kurahashi A, Sugimura T, Ushijima T. Construction of a high-throughput rat genetic mapping system with 466 arbitrarily primed-representational difference analysis markers. Mamm Genome. 2000;11:982-988.
-
(2000)
Mamm Genome
, vol.11
, pp. 982-988
-
-
Yamashita, S.1
Yoshida, Y.2
Kurahashi, A.3
Sugimura, T.4
Ushijima, T.5
-
12
-
-
0033582241
-
Development of the arbitrarily primed-representational difference analysis method and chromosomal mapping of isolated high throughput rat genetic markers
-
Yoshida Y, Ushijima T, Yamashita S, et al. Development of the arbitrarily primed-representational difference analysis method and chromosomal mapping of isolated high throughput rat genetic markers. Proc Natl Acad Sci USA. 1999;96:610-615.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 610-615
-
-
Yoshida, Y.1
Ushijima, T.2
Yamashita, S.3
-
13
-
-
0034652582
-
Chromosomal mapping of genes controlling development, histological grade, depth of invasion, and size of rat stomach carcinomas
-
Ushijima T, Yamamoto M, Suzui M, et al. Chromosomal mapping of genes controlling development, histological grade, depth of invasion, and size of rat stomach carcinomas. Cancer Res. 2000;60: 1092-1096.
-
(2000)
Cancer Res
, vol.60
, pp. 1092-1096
-
-
Ushijima, T.1
Yamamoto, M.2
Suzui, M.3
-
14
-
-
0023426747
-
Mapmaker: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations
-
Lander ES, Green P, Abrahamson J, et al. Mapmaker: an interactive computer package for constructing primary genetic linkage maps of experimental and natural populations. Genomics. 1987;1:174-181.
-
(1987)
Genomics
, vol.1
, pp. 174-181
-
-
Lander, E.S.1
Green, P.2
Abrahamson, J.3
-
15
-
-
0024293278
-
Resolution of quantitative traits into Mendelian factors by using a complete linkage map of restriction fragment length polymorphisms
-
Paterson AH, Lander ES, Hewitt JD, et al. Resolution of quantitative traits into Mendelian factors by using a complete linkage map of restriction fragment length polymorphisms. Nature. 1988;335: 721-726.
-
(1988)
Nature
, vol.335
, pp. 721-726
-
-
Paterson, A.H.1
Lander, E.S.2
Hewitt, J.D.3
-
16
-
-
0032931687
-
A radiation hybrid map of the rat genome containing 5,255 markers
-
Watanabe TK, Bihoreau MT, McCarthy LC, et al. A radiation hybrid map of the rat genome containing 5,255 markers. Nat Genet. 1999;22:27-36.
-
(1999)
Nat Genet
, vol.22
, pp. 27-36
-
-
Watanabe, T.K.1
Bihoreau, M.T.2
McCarthy, L.C.3
-
17
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander E, Kruglyak L. Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat Genet. 1995;11:241-247.
-
(1995)
Nat Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
18
-
-
0031959735
-
A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q
-
Shiels A, Mackay D, Ionides A, et al. A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q. Am J Hum Genet. 1998;62:526-532.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 526-532
-
-
Shiels, A.1
Mackay, D.2
Ionides, A.3
-
19
-
-
0032780886
-
Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin
-
Berry V, Mackay D, Khaliq S, et al. Connexin 50 mutation in a family with congenital "zonular nuclear" pulverulent cataract of Pakistani origin. Hum Genet. 1999;105:168-170.
-
(1999)
Hum Genet
, vol.105
, pp. 168-170
-
-
Berry, V.1
Mackay, D.2
Khaliq, S.3
-
20
-
-
0033365199
-
Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes
-
Annunen S, Korkko J, Czarny M, et al. Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes. Am J Hum Genet. 1999;65:974-983.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 974-983
-
-
Annunen, S.1
Korkko, J.2
Czarny, M.3
-
21
-
-
0033942141
-
A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2
-
Conley YP, Erturk D, Keverline A, et al. A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2. Am J Hum Genet. 2000;66:1426-1431.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1426-1431
-
-
Conley, Y.P.1
Erturk, D.2
Keverline, A.3
-
22
-
-
0033942142
-
Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2
-
Jakobs PM, Hess JF, FitzGerald PG, et al. Autosomal-dominant congenital cataract associated with a deletion mutation in the human beaded filament protein gene BFSP2. Am J Hum Genet. 2000;66:1432-1436.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1432-1436
-
-
Jakobs, P.M.1
Hess, J.F.2
FitzGerald, P.G.3
-
23
-
-
0032789891
-
Gap junctions containing alpha8-connexin (MP70) in the adult mammalian lens epithelium suggests a re-evaluation of its role in the lens
-
Dahm R, van Marle J, Prescott AR, Quinlan RA. Gap junctions containing alpha8-connexin (MP70) in the adult mammalian lens epithelium suggests a re-evaluation of its role in the lens. Exp Eye Res. 1999;69:45-56.
-
(1999)
Exp Eye Res
, vol.69
, pp. 45-56
-
-
Dahm, R.1
Van Marle, J.2
Prescott, A.R.3
Quinlan, R.A.4
-
24
-
-
0031658660
-
A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract
-
Steele EC Jr, Lyon MF, Favor J, et al. A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract. Curr Eye Res. 1998;17:883-889.
-
(1998)
Curr Eye Res
, vol.17
, pp. 883-889
-
-
Steele E.C., Jr.1
Lyon, M.F.2
Favor, J.3
-
25
-
-
0036501610
-
A Gja8 (Cx50) point mutation causes an alteration of alpha3 connexin (Cx46) in semi-dominant cataracts of LoplO mice
-
Chang B, Wang X, Hawes NL, et al. A Gja8 (Cx50) point mutation causes an alteration of alpha3 connexin (Cx46) in semi-dominant cataracts of LoplO mice. Hum Mol Genet. 2002;11:507-513.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 507-513
-
-
Chang, B.1
Wang, X.2
Hawes, N.L.3
-
26
-
-
0032476578
-
Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts
-
White TW, Goodenough DA, Paul DL. Targeted ablation of connexin50 in mice results in microphthalmia and zonular pulverulent cataracts. J Cell Biol. 1998;143:815-825.
-
(1998)
J Cell Biol
, vol.143
, pp. 815-825
-
-
White, T.W.1
Goodenough, D.A.2
Paul, D.L.3
-
27
-
-
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, et al. Disruption of Gja8 (alpha8 connexin) in mice leads to microphthalmia associated with retardation of lens growth and lens fiber maturation. Development. 2002;129:167-174.
-
(2002)
Development
, vol.129
, pp. 167-174
-
-
Rong, P.1
Wang, X.2
Niesman, I.3
-
28
-
-
0034080924
-
Connexin gene mutations in human genetic diseases
-
Krutovskikh V, Yamasaki H. Connexin gene mutations in human genetic diseases. Mutat Res. 2000;462:197-207.
-
(2000)
Mutat Res
, vol.462
, pp. 197-207
-
-
Krutovskikh, V.1
Yamasaki, H.2
-
29
-
-
0035253581
-
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts
-
Semina EV, Brownell I, Mintz-Hittner HA, Murray JC, Jamrich M. Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts. Hum Mol Genet. 2001;10:231-236.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 231-236
-
-
Semina, E.V.1
Brownell, I.2
Mintz-Hittner, H.A.3
Murray, J.C.4
Jamrich, M.5
-
30
-
-
0037059499
-
Unique and redundant connexin contributions to lens development
-
White TW. Unique and redundant connexin contributions to lens development. Science. 2002;295:319-320.
-
(2002)
Science
, vol.295
, pp. 319-320
-
-
White, T.W.1
|