-
1
-
-
84891600532
-
VSX1 mutation and corneal dystrophies
-
author reply 171 172
-
Aldave A J. VSX1 mutation and corneal dystrophies. Ophthalmology 2005 112 170-171; author reply 171 172
-
(2005)
Ophthalmology
, vol.112
, pp. 170-171
-
-
Aldave, A.J.1
-
3
-
-
19944416896
-
VSX1 mutational analysis in a series of Italian patients affected by keratoconus: Detection of a novel mutation.
-
Bisceglia L, Ciaschetti M, De Bonis P et al. VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation. Invest Ophthalmol Vis Sci 2005 46 39-45
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 39-45
-
-
Bisceglia, L.1
Ciaschetti, M.2
De Bonis, P.3
-
4
-
-
0035504694
-
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
-
Biswas S, Munier F L., Yardley J et al. Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy. Hum Mol Genet 2001 10 2415-2423
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2415-2423
-
-
Biswas, S.1
Munier, F.L.2
Yardley, J.3
-
5
-
-
0017692072
-
The clinical spectrum of posterior polymorphous dystrophy.
-
Cibis G W., Krachmer J A., Phelps C D. et al. The clinical spectrum of posterior polymorphous dystrophy. Arch Ophthalmol 1977 95 1529-1537
-
(1977)
Arch Ophthalmol
, vol.95
, pp. 1529-1537
-
-
Cibis, G.W.1
Krachmer, J.A.2
Phelps, C.D.3
-
6
-
-
33644805177
-
Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene.
-
Gwilliam R, Liskova P, Filipec M et al. Posterior polymorphous corneal dystrophy in Czech families maps to chromosome 20 and excludes the VSX1 gene. Invest Ophthalmol Vis Sci 2005 46 4480-4484
-
(2005)
Invest Ophthalmol Vis Sci
, vol.46
, pp. 4480-4484
-
-
Gwilliam, R.1
Liskova, P.2
Filipec, M.3
-
7
-
-
0034661280
-
RINX(VSX1), a novel homeobox gene expressed in the inner nuclear layer of the adult retina.
-
Hayashi T, Huang J, Deeb S S. RINX(VSX1), a novel homeobox gene expressed in the inner nuclear layer of the adult retina. Genomics 2000 67 128-139
-
(2000)
Genomics
, vol.67
, pp. 128-139
-
-
Hayashi, T.1
Huang, J.2
Deeb, S.S.3
-
8
-
-
0036566556
-
VSX1: A gene for posterior polymorphous dystrophy and keratoconus.
-
Heon E, Greenberg A, Kopp K K. et al. VSX1: a gene for posterior polymorphous dystrophy and keratoconus. Hum Mol Genet 2002 11 1029-1036
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1029-1036
-
-
Heon, E.1
Greenberg, A.2
Kopp, K.K.3
-
9
-
-
0028920471
-
Linkage of posterior polymorphous corneal dystrophy to 20q11.
-
Heon E, Mathers W D., Alward W L. et al. Linkage of posterior polymorphous corneal dystrophy to 20q11. Hum Mol Genet 1995 4 485-488
-
(1995)
Hum Mol Genet
, vol.4
, pp. 485-488
-
-
Heon, E.1
Mathers, W.D.2
Alward, W.L.3
-
10
-
-
33947095039
-
Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients.
-
Jirsova K, Merjava S, Martincova R et al. Immunohistochemical characterization of cytokeratins in the abnormal corneal endothelium of posterior polymorphous corneal dystrophy patients. Exp Eye Res 2007 84 680-686
-
(2007)
Exp Eye Res
, vol.84
, pp. 680-686
-
-
Jirsova, K.1
Merjava, S.2
Martincova, R.3
-
11
-
-
0022271735
-
Posterior polymorphous corneal dystrophy: A disease characterized by epithelial-like endothelial cells which influence management and prognosis.
-
Krachmer J H. Posterior polymorphous corneal dystrophy: a disease characterized by epithelial-like endothelial cells which influence management and prognosis. Trans Am Ophthalmol Soc 1985 83 413-475
-
(1985)
Trans Am Ophthalmol Soc
, vol.83
, pp. 413-475
-
-
Krachmer, J.H.1
-
12
-
-
0017895893
-
Corneal endothelial dystrophy. A study of 64 families.
-
Krachmer J H., Purcell J Jr, Young C W. et al. Corneal endothelial dystrophy. A study of 64 families. Arch Ophthalmol 1978 96 2036-2039
-
(1978)
Arch Ophthalmol
, vol.96
, pp. 2036-2039
-
-
Krachmer, J.H.1
Purcell Jr., J.2
Young, C.W.3
-
13
-
-
1842475539
-
VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells.
-
Mintz-Hittner H A., Semina E V., Frishman L J. et al. VSX1 (RINX) mutation with craniofacial anomalies, empty sella, corneal endothelial changes, and abnormal retinal and auditory bipolar cells. Ophthalmology 2004 111 828-836
-
(2004)
Ophthalmology
, vol.111
, pp. 828-836
-
-
Mintz-Hittner, H.A.1
Semina, E.V.2
Frishman, L.J.3
-
14
-
-
0031715039
-
Cloning of zebrafish vsx1: Expression of a paired-like homeobox gene during CNS development.
-
Passini M A., Kurtzman A L., Canger A K. et al. Cloning of zebrafish vsx1: expression of a paired-like homeobox gene during CNS development. Dev Genet 1998 23 128-141
-
(1998)
Dev Genet
, vol.23
, pp. 128-141
-
-
Passini, M.A.1
Kurtzman, A.L.2
Canger, A.K.3
-
15
-
-
0019250388
-
Epithelialization of the corneal endothelium in posterior polymorphous dystrophy.
-
Rodrigues M M., Sun T T., Krachmer J et al. Epithelialization of the corneal endothelium in posterior polymorphous dystrophy. Invest Ophthalmol Vis Sci 1980 19 832-835
-
(1980)
Invest Ophthalmol Vis Sci
, vol.19
, pp. 832-835
-
-
Rodrigues, M.M.1
Sun, T.T.2
Krachmer, J.3
-
17
-
-
0034234546
-
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice.
-
Semina E V., Murray J C., Reiter R et al. Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. Hum Mol Genet 2000 9 1575-1585
-
(2000)
Hum Mol Genet
, vol.9
, pp. 1575-1585
-
-
Semina, E.V.1
Murray, J.C.2
Reiter, R.3
-
18
-
-
7444226218
-
A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.
-
Shimizu S, Krafchak C, Fuse N et al. A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10. Am J Med Genet A 2004 130A 372-377
-
(2004)
Am J Med Genet A
, vol.130
, pp. 372-377
-
-
Shimizu, S.1
Krafchak, C.2
Fuse, N.3
-
19
-
-
33749148802
-
A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32.
-
Sundin O H., Broman K W., Chang H H. et al. A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32. Invest Ophthalmol Vis Sci 2006 47 3919-3926
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 3919-3926
-
-
Sundin, O.H.1
Broman, K.W.2
Chang, H.H.3
-
20
-
-
33644843021
-
Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13 pTel-13q12.13.
-
Sundin O H., Jun A S., Broman K W. et al. Linkage of late-onset Fuchs corneal dystrophy to a novel locus at 13 pTel-13q12.13. Invest Ophthalmol Vis Sci 2006 47 140-145
-
(2006)
Invest Ophthalmol Vis Sci
, vol.47
, pp. 140-145
-
-
Sundin, O.H.1
Jun, A.S.2
Broman, K.W.3
-
21
-
-
65349167054
-
The IC 3D Classification of the Corneal Dystrophies.
-
Weiss J S MH, Lisch W, Kinoshita S et al. The IC 3D Classification of the Corneal Dystrophies. Cornea 2008 27 S1-S42
-
(2008)
Cornea
, vol.27
-
-
Weiss, J.S.M.1
Lisch, W.2
Kinoshita, S.3
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