-
1
-
-
0026545407
-
A temporally regulated, diffusible activity is required for rod photoreceptor development in vitro
-
(1992)
Development
, vol.114
, pp. 947-957
-
-
Altshuler, D.1
Cepko, C.2
-
5
-
-
0030587607
-
Correlations between terminal mitosis and differentiated fate of retinal precursor cells in vivo and in vitro: Analysis with the "window-labeling" technique
-
(1996)
Dev. Biol.
, vol.178
, pp. 304-315
-
-
Belecky-Adams, T.1
Cook, B.2
Adler, R.3
-
12
-
-
0031800728
-
Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome
-
(1998)
Nat. Genet.
, vol.19
, pp. 47-50
-
-
Dreyer, S.D.1
Zhou, G.2
Baldini, A.3
Winterpacht, A.4
Zabel, B.5
Cole, W.6
Johnson, R.L.7
Lee, B.8
-
14
-
-
0031458813
-
Pax6 controls progenitor cell identity and neuronal fate in response to graded Shh signaling
-
(1997)
Cell
, vol.90
, pp. 169-180
-
-
Ericson, J.1
Rashbass, P.2
Schedl, A.3
Brenner-Morton, S.4
Kawakami, A.5
Van Heyningen, V.6
Jessell, T.M.7
Briscoe, J.8
-
19
-
-
0031043428
-
Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 457-464
-
-
Gage, P.J.1
Camper, S.A.2
-
20
-
-
0032826288
-
Genomic cloning and characterization of the human homeobox gene SIX6 reveals a cluster of SIX genes in chromosome 14 and associates SIX6 hemizygosity with bilateral anophthalmia and pituitary anomalies
-
(1999)
Genomics
, vol.61
, pp. 82-91
-
-
Gallardo, M.E.1
Lopez-Rios, J.2
Fernaud-Espinosa, I.3
Granadino, B.4
Sanz, R.5
Ramos, C.6
Ayuso, C.7
Seller, M.J.8
Brunner, H.G.9
Bovolenta, P.10
Rodriguez de Cordoba, S.11
-
22
-
-
0014009334
-
Role of the lens in the morphogenesis of the iris and cornea
-
(1966)
Nature
, vol.210
, pp. 209-210
-
-
Genis-Galvez, J.M.1
-
25
-
-
0026800666
-
Embryonic lens induction: Shedding light on vertebrate tissue determination
-
(1992)
Trends Genet.
, vol.8
, pp. 349-355
-
-
Grainger, R.M.1
-
26
-
-
0029929286
-
Genetic aspects of embryonic eye development in vertebrates
-
(1996)
Dev. Genet.
, vol.18
, pp. 181-197
-
-
Graw, J.1
-
29
-
-
0026345992
-
Mouse small eye results from mutations in a paired-like homeobox-containing gene
-
(1991)
Nature
, vol.354
, pp. 522-525
-
-
Hill, R.E.1
Favor, J.2
Hogan, B.L.3
Ton, C.C.4
Saunders, G.F.5
Hanson, I.M.6
Prosser, J.7
Jordan, T.8
Hastie, N.D.9
Van Heyningen, V.10
-
32
-
-
0022240737
-
Monoclonal antibody against chicken type IX collagen: Preparation, characterization, and recognition of the intact form of type IX collagen secreted by chondrocytes
-
(1985)
J. Cell Biol.
, vol.101
, pp. 814-823
-
-
Irwin, M.H.1
Silvers, S.H.2
Mayne, R.3
-
33
-
-
0032804010
-
Six6 (Optx2) is a novel murine Six3-related homeobox gene that demarcates the presumptive pituitary/hypothalamic axis and the ventral optic stalk
-
(1999)
Mech. Dev.
, vol.84
, pp. 31-40
-
-
Jean, D.1
Bernier, G.2
Gruss, P.3
-
44
-
-
0032575555
-
The cloning of mouse keratocan cDNA and genomic DNA and the characterization of its expression during eye development
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 22584-22588
-
-
Liu, C.Y.1
Shiraishi, A.2
Kao, C.W.3
Converse, R.L.4
Funderburgh, J.L.5
Corpuz, L.M.6
Conrad, G.W.7
Kao, W.W.8
-
48
-
-
0032471924
-
Mutation analysis of LMX1B gene in nail-patella syndrome patients
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1651-1658
-
-
McIntosh, I.1
Dreyer, S.D.2
Clough, M.V.3
Dunston, J.A.4
Eyaid, W.5
Roig, C.M.6
Montgomery, T.7
Ala-Mello, S.8
Kaitila, I.9
Winterpacht, A.10
Zabel, B.11
Frydman, M.12
Cole, W.G.13
Francomano, C.A.14
Lee, B.15
-
49
-
-
0032231330
-
Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 1316-1328
-
-
Mears, A.J.1
Jordan, T.2
Mirzayans, F.3
Dubois, S.4
Kume, T.5
Parlee, M.6
Ritch, R.7
Koop, B.8
Kuo, W.L.9
Collins, C.10
Marshall, J.11
Gould, D.B.12
Pearce, W.13
Carlsson, P.14
Enerback, S.15
Morissette, J.16
Bhattacharya, S.17
Hogan, B.18
Raymond, V.19
Walter, M.A.20
more..
-
53
-
-
0035125059
-
A spectrum of FOXC1 mutations suggests gene dosage as a mechanism for developmental defects of the anterior chamber of the eye
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 364-372
-
-
Nishimura, D.Y.1
Searby, C.C.2
Alward, W.L.3
Walton, D.4
Craig, J.E.5
Mackey, D.A.6
Kawase, K.7
Kanis, A.B.8
Patil, S.R.9
Stone, E.M.10
Sheffield, V.C.11
-
54
-
-
17344368672
-
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
-
(1998)
Nat. Genet.
, vol.19
, pp. 140-147
-
-
Nishimura, D.Y.1
Swiderski, R.E.2
Alward, W.L.3
Searby, C.C.4
Patil, S.R.5
Bennet, S.R.6
Kanis, A.B.7
Gastier, J.M.8
Stone, E.M.9
Sheffield, V.C.10
-
57
-
-
0029617682
-
Six3, a murine homologue of the sine oculis gene, demarcates the most anterior border of the developing neural plate and is expressed during eye development
-
(1995)
Development
, vol.121
, pp. 4045-4055
-
-
Oliver, G.1
Mailhos, A.2
Wehr, R.3
Copeland, N.G.4
Jenkins, N.A.5
Gruss, P.6
-
59
-
-
0034117963
-
Mutations in KERA, encoding keratocan, cause cornea plana
-
(2000)
Nat. Genet.
, vol.25
, pp. 91-95
-
-
Pellegata, N.S.1
Dieguez-Lucena, J.L.2
Joensuu, T.3
Lau, S.4
Montgomery, K.T.5
Krahe, R.6
Kivela, T.7
Kucherlapati, R.8
Forsius, H.9
De la Chapelle, A.10
-
61
-
-
0034090670
-
LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye
-
(2000)
Genesis
, vol.26
, pp. 15-25
-
-
Pressman, C.L.1
Chen, H.2
Johnson, R.L.3
-
68
-
-
0034103010
-
Heterozygous loss of Six5 in mice is sufficient to cause ocular cataracts
-
(2000)
Nat. Genet.
, vol.25
, pp. 110-114
-
-
Sarkar, P.S.1
Appukuttan, B.2
Han, J.3
Ito, Y.4
Ai, C.5
Tsai, W.6
Chai, Y.7
Stout, J.T.8
Reddy, S.9
-
70
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene. RIEG, involved in Rieger syndrome
-
(1996)
Nat. Genet.
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Alward, W.L.4
Small, K.W.5
Datson, N.A.6
Siegel-Bartelt, J.7
Bierke-Nelson, D.8
Bitoun, P.9
Zabel, B.U.10
Carey, J.C.11
Murray, J.C.12
-
72
-
-
18144437181
-
Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1021-1032
-
-
Smith, R.S.1
Zabaleta, A.2
Kume, T.3
Savinova, O.V.4
Kidson, S.H.5
Martin, J.E.6
Nishimura, D.Y.7
Alward, W.L.8
Hogan, B.L.9
John, S.W.10
-
76
-
-
0029068775
-
Cranial paraxial mesoderm and neural crest cells of the mouse embryo: Co-distribution in the craniofacial mesenchyme but distinct segregation in branchial arches
-
(1995)
Development
, vol.121
, pp. 2569-2582
-
-
Trainor, P.A.1
Tam, P.P.2
-
77
-
-
0031750061
-
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 1091-1098
-
-
Vollrath, D.1
Jaramillo-Babb, V.L.2
Clough, M.V.3
McIntosh, I.4
Scott, K.M.5
Lichter, P.R.6
Richards, J.E.7
-
78
-
-
0033064156
-
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
-
(1999)
Nat. Genet.
, vol.22
, pp. 196-198
-
-
Wallis, D.E.1
Roessler, E.2
Hehr, U.3
Nanni, L.4
Wiltshire, T.5
Richieri-Costa, A.6
Gillessen-Kaesbach, G.7
Zackai, E.H.8
Rommens, J.9
Muenke, M.10
-
82
-
-
0029839804
-
Flk-1, a receptor for vascular endothelial growth factor (VEGF), is expressed by retinal progenitor cells
-
(1996)
J. Neurosci.
, vol.16
, pp. 6089-6099
-
-
Yang, X.J.1
Cepko, C.L.2
|