-
1
-
-
0028936980
-
Lens aplasia: a new mutation producing lens abnormality in the mouse
-
Aso S., Horiwaki S., and Noda S. Lens aplasia: a new mutation producing lens abnormality in the mouse. Lab. Anim. Sci. 45 (1995) 41-46
-
(1995)
Lab. Anim. Sci.
, vol.45
, pp. 41-46
-
-
Aso, S.1
Horiwaki, S.2
Noda, S.3
-
2
-
-
0034030689
-
Hypoplastic basement membrane of the lens anlage in the inheritable lens aplastic mouse (lap mouse)
-
Aso S., Baba R., Noda S., Ikuno S., and Fujita M. Hypoplastic basement membrane of the lens anlage in the inheritable lens aplastic mouse (lap mouse). Teratology 61 (2000) 262-272
-
(2000)
Teratology
, vol.61
, pp. 262-272
-
-
Aso, S.1
Baba, R.2
Noda, S.3
Ikuno, S.4
Fujita, M.5
-
3
-
-
0030468324
-
Genetic dissection of the retinotectal projection
-
Baier H., Klostermann S., Trowe T., Karlstrom R.O., Nusslein-Volhard C., and Bonhoeffer F. Genetic dissection of the retinotectal projection. Development 123 (1996) 415-425
-
(1996)
Development
, vol.123
, pp. 415-425
-
-
Baier, H.1
Klostermann, S.2
Trowe, T.3
Karlstrom, R.O.4
Nusslein-Volhard, C.5
Bonhoeffer, F.6
-
4
-
-
0034656096
-
The lens organizes the anterior segment: specification of neural crest cell differentiation in the avian eye
-
Beebe D.C., and Coats J.M. The lens organizes the anterior segment: specification of neural crest cell differentiation in the avian eye. Dev. Biol. 220 (2000) 424-431
-
(2000)
Dev. Biol.
, vol.220
, pp. 424-431
-
-
Beebe, D.C.1
Coats, J.M.2
-
5
-
-
0345550397
-
FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies
-
Beggs H.E., Schahin-Reed D., Zang K., Goebbels S., Nave K.A., Gorski J., Jones K.R., Sretavan D., and Reichardt L.F. FAK deficiency in cells contributing to the basal lamina results in cortical abnormalities resembling congenital muscular dystrophies. Neuron 40 (2003) 501-514
-
(2003)
Neuron
, vol.40
, pp. 501-514
-
-
Beggs, H.E.1
Schahin-Reed, D.2
Zang, K.3
Goebbels, S.4
Nave, K.A.5
Gorski, J.6
Jones, K.R.7
Sretavan, D.8
Reichardt, L.F.9
-
6
-
-
0034650544
-
A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle
-
Blixt A., Mahlapuu M., Aitola M., Pelto-Huikko M., Enerback S., and Carlsson P. A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle. Genes Dev. 14 (2000) 245-254
-
(2000)
Genes Dev.
, vol.14
, pp. 245-254
-
-
Blixt, A.1
Mahlapuu, M.2
Aitola, M.3
Pelto-Huikko, M.4
Enerback, S.5
Carlsson, P.6
-
7
-
-
33745261734
-
Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly
-
Breedveld G., de Coo R.F., Lequin M.H., Arts W.F., Heutink P., Gould D.B., John S.W., Oostra B., and Mancini G.M. Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly. J. Med. Genet. (2006)
-
(2006)
J. Med. Genet.
-
-
Breedveld, G.1
de Coo, R.F.2
Lequin, M.H.3
Arts, W.F.4
Heutink, P.5
Gould, D.B.6
John, S.W.7
Oostra, B.8
Mancini, G.M.9
-
8
-
-
0033897180
-
Forkhead Foxe3 maps to the dysgenetic lens locus and is critical in lens development and differentiation
-
Brownell I., Dirksen M., and Jamrich M. Forkhead Foxe3 maps to the dysgenetic lens locus and is critical in lens development and differentiation. Genesis 27 (2000) 81-93
-
(2000)
Genesis
, vol.27
, pp. 81-93
-
-
Brownell, I.1
Dirksen, M.2
Jamrich, M.3
-
9
-
-
0034075654
-
Form and function: the laminin family of heterotrimers
-
Colognato H., and Yurchenco P.D. Form and function: the laminin family of heterotrimers. Dev. Dyn. 218 (2000) 213-234
-
(2000)
Dev. Dyn.
, vol.218
, pp. 213-234
-
-
Colognato, H.1
Yurchenco, P.D.2
-
10
-
-
0041468624
-
Activity and distribution of paxillin, focal adhesion kinase, and cadherin indicate cooperative roles during zebrafish morphogenesis
-
Crawford B.D., Henry C.A., Clason T.A., Becker A.L., and Hille M.B. Activity and distribution of paxillin, focal adhesion kinase, and cadherin indicate cooperative roles during zebrafish morphogenesis. Mol. Biol. Cell 14 (2003) 3065-3081
-
(2003)
Mol. Biol. Cell
, vol.14
, pp. 3065-3081
-
-
Crawford, B.D.1
Henry, C.A.2
Clason, T.A.3
Becker, A.L.4
Hille, M.B.5
-
11
-
-
17744397133
-
pitx3 defines an equivalence domain for lens and anterior pituitary placode
-
Dutta S., Dietrich J.E., Aspock G., Burdine R.D., Schier A., Westerfield M., and Varga Z.M. pitx3 defines an equivalence domain for lens and anterior pituitary placode. Development 132 (2005) 1579-1590
-
(2005)
Development
, vol.132
, pp. 1579-1590
-
-
Dutta, S.1
Dietrich, J.E.2
Aspock, G.3
Burdine, R.D.4
Schier, A.5
Westerfield, M.6
Varga, Z.M.7
-
12
-
-
0032715703
-
Restricted distribution of laminin alpha1 chain in normal adult mouse tissues
-
Falk M., Ferletta M., Forsberg E., and Ekblom P. Restricted distribution of laminin alpha1 chain in normal adult mouse tissues. Matrix Biol. 18 (1999) 557-568
-
(1999)
Matrix Biol.
, vol.18
, pp. 557-568
-
-
Falk, M.1
Ferletta, M.2
Forsberg, E.3
Ekblom, P.4
-
13
-
-
18444389460
-
Lack of collagen XVIII/endostatin results in eye abnormalities
-
Fukai N., Eklund L., Marneros A.G., Oh S.P., Keene D.R., Tamarkin L., Niemela M., Ilves M., Li E., Pihlajaniemi T., and Olsen B.R. Lack of collagen XVIII/endostatin results in eye abnormalities. EMBO J. 21 (2002) 1535-1544
-
(2002)
EMBO J.
, vol.21
, pp. 1535-1544
-
-
Fukai, N.1
Eklund, L.2
Marneros, A.G.3
Oh, S.P.4
Keene, D.R.5
Tamarkin, L.6
Niemela, M.7
Ilves, M.8
Li, E.9
Pihlajaniemi, T.10
Olsen, B.R.11
-
14
-
-
15944376601
-
New perspectives on eye development and the evolution of eyes and photoreceptors
-
Gehring W.J. New perspectives on eye development and the evolution of eyes and photoreceptors. J. Heredity 96 (2005) 171-184
-
(2005)
J. Heredity
, vol.96
, pp. 171-184
-
-
Gehring, W.J.1
-
15
-
-
0014009334
-
Role of the lens in the morphogenesis of the iris and cornea
-
Genis-Galvez J.M. Role of the lens in the morphogenesis of the iris and cornea. Nature 210 (1966) 209-210
-
(1966)
Nature
, vol.210
, pp. 209-210
-
-
Genis-Galvez, J.M.1
-
16
-
-
0037326951
-
The zebrafish as a tool for understanding the biology of visual disorders
-
Goldsmith P., and Harris W.A. The zebrafish as a tool for understanding the biology of visual disorders. Semin. Cell Dev. Biol. 14 (2003) 11-18
-
(2003)
Semin. Cell Dev. Biol.
, vol.14
, pp. 11-18
-
-
Goldsmith, P.1
Harris, W.A.2
-
17
-
-
33644815534
-
Fuchs corneal dystrophy: aberrant collagen distribution in an L450W mutant of the COL8A2 gene
-
Gottsch J.D., Zhang C., Sundin O.H., Bell W.R., Stark W.J., and Green W.R. Fuchs corneal dystrophy: aberrant collagen distribution in an L450W mutant of the COL8A2 gene. Invest. Ophthalmol. Visual Sci. 46 (2005) 4504-4511
-
(2005)
Invest. Ophthalmol. Visual Sci.
, vol.46
, pp. 4504-4511
-
-
Gottsch, J.D.1
Zhang, C.2
Sundin, O.H.3
Bell, W.R.4
Stark, W.J.5
Green, W.R.6
-
18
-
-
4744376027
-
Genetically increasing Myoc expression supports a necessary pathologic role of abnormal proteins in glaucoma
-
Gould D.B., Miceli-Libby L., Savinova O.V., Torrado M., Tomarev S.I., Smith R.S., and John S.W. Genetically increasing Myoc expression supports a necessary pathologic role of abnormal proteins in glaucoma. Mol. Cell. Biol. 24 (2004) 9019-9025
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 9019-9025
-
-
Gould, D.B.1
Miceli-Libby, L.2
Savinova, O.V.3
Torrado, M.4
Tomarev, S.I.5
Smith, R.S.6
John, S.W.7
-
19
-
-
11144294168
-
Anterior segment development relevant to glaucoma
-
Gould D.B., Smith R.S., and John S.W. Anterior segment development relevant to glaucoma. Int. J. Dev. Biol. 48 (2004) 1015-1029
-
(2004)
Int. J. Dev. Biol.
, vol.48
, pp. 1015-1029
-
-
Gould, D.B.1
Smith, R.S.2
John, S.W.3
-
20
-
-
21044442223
-
Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly
-
Gould D.B., Phalan F.C., Breedveld G.J., van Mil S.E., Smith R.S., Schimenti J.C., Aguglia U., van der Knaap M.S., Heutink P., and John S.W. Mutations in Col4a1 cause perinatal cerebral hemorrhage and porencephaly. Science 308 (2005) 1167-1171
-
(2005)
Science
, vol.308
, pp. 1167-1171
-
-
Gould, D.B.1
Phalan, F.C.2
Breedveld, G.J.3
van Mil, S.E.4
Smith, R.S.5
Schimenti, J.C.6
Aguglia, U.7
van der Knaap, M.S.8
Heutink, P.9
John, S.W.10
-
21
-
-
11144298645
-
Congenital hereditary cataracts
-
Graw J. Congenital hereditary cataracts. Int. J. Dev. Biol. 48 (2004) 1031-1044
-
(2004)
Int. J. Dev. Biol.
, vol.48
, pp. 1031-1044
-
-
Graw, J.1
-
22
-
-
0037351438
-
Developmental genetics in ophthalmology
-
Graw J., and Loster J. Developmental genetics in ophthalmology. Ophthalmic Genet. 24 (2003) 1-33
-
(2003)
Ophthalmic Genet.
, vol.24
, pp. 1-33
-
-
Graw, J.1
Loster, J.2
-
23
-
-
84907115386
-
Congenital cataract with microcornea and Peters' anomaly as expressions of one autosomal dominant gene
-
Green J.S., and Johnson G.J. Congenital cataract with microcornea and Peters' anomaly as expressions of one autosomal dominant gene. Ophthalmic Paediatr. Genet. 7 (1986) 187-194
-
(1986)
Ophthalmic Paediatr. Genet.
, vol.7
, pp. 187-194
-
-
Green, J.S.1
Johnson, G.J.2
-
24
-
-
0031659016
-
Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8
-
Grimes P.A., Koeberlein B., Favor J., Neuhauser-Klaus A., and Stambolian D. Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8. Invest. Ophthalmol. Visual Sci. 39 (1998) 1863-1869
-
(1998)
Invest. Ophthalmol. Visual Sci.
, vol.39
, pp. 1863-1869
-
-
Grimes, P.A.1
Koeberlein, B.2
Favor, J.3
Neuhauser-Klaus, A.4
Stambolian, D.5
-
25
-
-
20444401225
-
Identification of zebrafish insertional mutants with defects in visual system development and function
-
Gross J.M., Perkins B.D., Amsterdam A., Egana A., Darland T., Matsui J.I., Sciascia S., Hopkins N., and Dowling J.E. Identification of zebrafish insertional mutants with defects in visual system development and function. Genetics 170 (2005) 245-261
-
(2005)
Genetics
, vol.170
, pp. 245-261
-
-
Gross, J.M.1
Perkins, B.D.2
Amsterdam, A.3
Egana, A.4
Darland, T.5
Matsui, J.I.6
Sciascia, S.7
Hopkins, N.8
Dowling, J.E.9
-
26
-
-
0032551513
-
Disruption of the retinal basal lamina during early embryonic development leads to a retraction of vitreal end feet, an increased number of ganglion cells, and aberrant axonal outgrowth
-
Halfter W. Disruption of the retinal basal lamina during early embryonic development leads to a retraction of vitreal end feet, an increased number of ganglion cells, and aberrant axonal outgrowth. J. Comp. Neurol. 397 (1998) 89-104
-
(1998)
J. Comp. Neurol.
, vol.397
, pp. 89-104
-
-
Halfter, W.1
-
27
-
-
0035894523
-
Roles for zebrafish focal adhesion kinase in notochord and somite morphogenesis
-
Henry C.A., Crawford B.D., Yan Y.L., Postlethwait J., Cooper M.S., and Hille M.B. Roles for zebrafish focal adhesion kinase in notochord and somite morphogenesis. Dev. Biol. 240 (2001) 474-487
-
(2001)
Dev. Biol.
, vol.240
, pp. 474-487
-
-
Henry, C.A.1
Crawford, B.D.2
Yan, Y.L.3
Postlethwait, J.4
Cooper, M.S.5
Hille, M.B.6
-
28
-
-
23444448102
-
Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye
-
Hopfer U., Fukai N., Hopfer H., Wolf G., Joyce N., Li E., and Olsen B.R. Targeted disruption of Col8a1 and Col8a2 genes in mice leads to anterior segment abnormalities in the eye. FASEB J. 19 (2005) 1232-1244
-
(2005)
FASEB J.
, vol.19
, pp. 1232-1244
-
-
Hopfer, U.1
Fukai, N.2
Hopfer, H.3
Wolf, G.4
Joyce, N.5
Li, E.6
Olsen, B.R.7
-
29
-
-
0038642451
-
Optic cup morphogenesis requires pre-lens ectoderm but not lens differentiation
-
Hyer J., Kuhlman J., Afif E., and Mikawa T. Optic cup morphogenesis requires pre-lens ectoderm but not lens differentiation. Dev. Biol. 259 (2003) 351-363
-
(2003)
Dev. Biol.
, vol.259
, pp. 351-363
-
-
Hyer, J.1
Kuhlman, J.2
Afif, E.3
Mikawa, T.4
-
30
-
-
0036156544
-
Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma
-
Jamieson R.V., Perveen R., Kerr B., Carette M., Yardley J., Heon E., Wirth M.G., van Heyningen V., Donnai D., Munier F., and Black G.C. Domain disruption and mutation of the bZIP transcription factor, MAF, associated with cataract, ocular anterior segment dysgenesis and coloboma. Hum. Mol. Genet. 11 (2002) 33-42
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 33-42
-
-
Jamieson, R.V.1
Perveen, R.2
Kerr, B.3
Carette, M.4
Yardley, J.5
Heon, E.6
Wirth, M.G.7
van Heyningen, V.8
Donnai, D.9
Munier, F.10
Black, G.C.11
-
31
-
-
3242685047
-
Age-related macular degeneration and the extracellular matrix
-
Johnson L.V., and Anderson D.H. Age-related macular degeneration and the extracellular matrix. N. Engl. J. Med. 351 (2004) 320-322
-
(2004)
N. Engl. J. Med.
, vol.351
, pp. 320-322
-
-
Johnson, L.V.1
Anderson, D.H.2
-
32
-
-
0029045033
-
Stages of embryonic development of the zebrafish
-
Kimmel C.B., Ballard W.W., Kimmel S.R., Ullmann B., and Schilling T.F. Stages of embryonic development of the zebrafish. Dev. Dyn. 203 (1995) 253-310
-
(1995)
Dev. Dyn.
, vol.203
, pp. 253-310
-
-
Kimmel, C.B.1
Ballard, W.W.2
Kimmel, S.R.3
Ullmann, B.4
Schilling, T.F.5
-
33
-
-
0030857559
-
Disulfide-bonding between Drosophila laminin beta and gamma chains is essential for alpha chain to form alpha betagamma trimer
-
Kumagai C., Kadowaki T., and Kitagawa Y. Disulfide-bonding between Drosophila laminin beta and gamma chains is essential for alpha chain to form alpha betagamma trimer. FEBS Lett. 412 (1997) 211-216
-
(1997)
FEBS Lett.
, vol.412
, pp. 211-216
-
-
Kumagai, C.1
Kadowaki, T.2
Kitagawa, Y.3
-
34
-
-
0036039827
-
In vivo imaging of embryonic vascular development using transgenic zebrafish
-
Lawson N.D., and Weinstein B.M. In vivo imaging of embryonic vascular development using transgenic zebrafish. Dev. Biol. 248 (2002) 307-318
-
(2002)
Dev. Biol.
, vol.248
, pp. 307-318
-
-
Lawson, N.D.1
Weinstein, B.M.2
-
35
-
-
0033216631
-
Disruption of laminin beta2 chain production causes alterations in morphology and function in the CNS
-
Libby R.T., Lavallee C.R., Balkema G.W., Brunken W.J., and Hunter D.D. Disruption of laminin beta2 chain production causes alterations in morphology and function in the CNS. J. Neurosci. 19 (1999) 9399-9411
-
(1999)
J. Neurosci.
, vol.19
, pp. 9399-9411
-
-
Libby, R.T.1
Lavallee, C.R.2
Balkema, G.W.3
Brunken, W.J.4
Hunter, D.D.5
-
36
-
-
0034279184
-
Laminin expression in adult and developing retinae: evidence of two novel CNS laminins
-
Libby R.T., Champliaud M.F., Claudepierre T., Xu Y., Gibbons E.P., Koch M., Burgeson R.E., Hunter D.D., and Brunken W.J. Laminin expression in adult and developing retinae: evidence of two novel CNS laminins. J. Neurosci. 20 (2000) 6517-6528
-
(2000)
J. Neurosci.
, vol.20
, pp. 6517-6528
-
-
Libby, R.T.1
Champliaud, M.F.2
Claudepierre, T.3
Xu, Y.4
Gibbons, E.P.5
Koch, M.6
Burgeson, R.E.7
Hunter, D.D.8
Brunken, W.J.9
-
37
-
-
0034082512
-
The zebrafish young mutation acts non-cell-autonomously to uncouple differentiation from specification for all retinal cells
-
Link B.A., Fadool J.M., Malicki J., and Dowling J.E. The zebrafish young mutation acts non-cell-autonomously to uncouple differentiation from specification for all retinal cells. Development 127 (2000) 2177-2188
-
(2000)
Development
, vol.127
, pp. 2177-2188
-
-
Link, B.A.1
Fadool, J.M.2
Malicki, J.3
Dowling, J.E.4
-
38
-
-
4243754390
-
Isolation of zebrafish mutations that affect the development and maintenance of the lens
-
[Abstract]
-
Link B.A., Darland T., and Dowling J.E. Isolation of zebrafish mutations that affect the development and maintenance of the lens. [Abstract]. Invest. Ophthalmol. Visual Sci. 42 (2001) S537
-
(2001)
Invest. Ophthalmol. Visual Sci.
, vol.42
-
-
Link, B.A.1
Darland, T.2
Dowling, J.E.3
-
39
-
-
9444223950
-
Intraocular pressure in zebrafish: comparison of inbred strains and identification of a reduced melanin mutant with raised IOP
-
Link B.A., Gray M.P., Smith R.S., and John S.W. Intraocular pressure in zebrafish: comparison of inbred strains and identification of a reduced melanin mutant with raised IOP. Invest. Ophthalmol. Visual Sci. 45 (2004) 4415-4422
-
(2004)
Invest. Ophthalmol. Visual Sci.
, vol.45
, pp. 4415-4422
-
-
Link, B.A.1
Gray, M.P.2
Smith, R.S.3
John, S.W.4
-
40
-
-
18144404148
-
Physiological role of collagen XVIII and endostatin
-
Marneros A.G., and Olsen B.R. Physiological role of collagen XVIII and endostatin. FASEB J. 19 (2005) 716-728
-
(2005)
FASEB J.
, vol.19
, pp. 716-728
-
-
Marneros, A.G.1
Olsen, B.R.2
-
41
-
-
13444301115
-
Structure and laminin-binding specificity of the NtA domain expressed in eukaryotic cells
-
Mascarenhas J.B., Ruegg M.A., Sasaki T., Eble J.A., Engel J., and Stetefeld J. Structure and laminin-binding specificity of the NtA domain expressed in eukaryotic cells. Matrix Biol. 23 (2005) 507-513
-
(2005)
Matrix Biol.
, vol.23
, pp. 507-513
-
-
Mascarenhas, J.B.1
Ruegg, M.A.2
Sasaki, T.3
Eble, J.A.4
Engel, J.5
Stetefeld, J.6
-
43
-
-
7944231499
-
Using zebrafish to study the complex genetics of glaucoma
-
McMahon C., Semina E.V., and Link B.A. Using zebrafish to study the complex genetics of glaucoma. Comp. Biochem. Physiol. 138 (2004) 343-350
-
(2004)
Comp. Biochem. Physiol.
, vol.138
, pp. 343-350
-
-
McMahon, C.1
Semina, E.V.2
Link, B.A.3
-
44
-
-
0035504763
-
Understanding human disease mutations through the use of interspecific genetic variation
-
Miller M.P., and Kumar S. Understanding human disease mutations through the use of interspecific genetic variation. Hum. Mol. Genet. 10 (2001) 2319-2328
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2319-2328
-
-
Miller, M.P.1
Kumar, S.2
-
45
-
-
3042790010
-
Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation
-
Miner J.H., Li C., Mudd J.L., Go G., and Sutherland A.E. Compositional and structural requirements for laminin and basement membranes during mouse embryo implantation and gastrulation. Development 131 (2004) 2247-2256
-
(2004)
Development
, vol.131
, pp. 2247-2256
-
-
Miner, J.H.1
Li, C.2
Mudd, J.L.3
Go, G.4
Sutherland, A.E.5
-
46
-
-
0036237994
-
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
-
Ormestad M., Blixt A., Churchill A., Martinsson T., Enerback S., and Carlsson P. Foxe3 haploinsufficiency in mice: a model for Peters' anomaly. Invest. Ophthalmol. Visual Sci. 43 (2002) 1350-1357
-
(2002)
Invest. Ophthalmol. Visual Sci.
, vol.43
, pp. 1350-1357
-
-
Ormestad, M.1
Blixt, A.2
Churchill, A.3
Martinsson, T.4
Enerback, S.5
Carlsson, P.6
-
47
-
-
0037509990
-
Focal adhesion kinase: the first ten years
-
Parsons J.T. Focal adhesion kinase: the first ten years. J. Cell Sci. 116 (2003) 1409-1416
-
(2003)
J. Cell Sci.
, vol.116
, pp. 1409-1416
-
-
Parsons, J.T.1
-
48
-
-
0036333446
-
Zebrafish mutants identify an essential role for laminins in notochord formation
-
Parsons M.J., Pollard S.M., Saude L., Feldman B., Coutinho P., Hirst E.M., and Stemple D.L. Zebrafish mutants identify an essential role for laminins in notochord formation. Development 129 (2002) 3137-3146
-
(2002)
Development
, vol.129
, pp. 3137-3146
-
-
Parsons, M.J.1
Pollard, S.M.2
Saude, L.3
Feldman, B.4
Coutinho, P.5
Hirst, E.M.6
Stemple, D.L.7
-
49
-
-
33644971971
-
Zebrafish bashful/laminin-alpha1 mutants exhibit multiple axon guidance defects
-
Paulus J.D., and Halloran M.C. Zebrafish bashful/laminin-alpha1 mutants exhibit multiple axon guidance defects. Dev. Dyn. 235 (2006) 213-224
-
(2006)
Dev. Dyn.
, vol.235
, pp. 213-224
-
-
Paulus, J.D.1
Halloran, M.C.2
-
50
-
-
29144519398
-
Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation
-
Pollard S.M., Parsons M.J., Kamei M., Kettleborough R.N., Thomas K.A., Pham V.N., Bae M.K., Scott A., Weinstein B.M., and Stemple D.L. Essential and overlapping roles for laminin alpha chains in notochord and blood vessel formation. Dev. Biol. (2006)
-
(2006)
Dev. Biol.
-
-
Pollard, S.M.1
Parsons, M.J.2
Kamei, M.3
Kettleborough, R.N.4
Thomas, K.A.5
Pham, V.N.6
Bae, M.K.7
Scott, A.8
Weinstein, B.M.9
Stemple, D.L.10
-
51
-
-
0033960925
-
Formation of corneal endothelium is essential for anterior segment development-A transgenic mouse model of anterior segment dysgenesis
-
Reneker L.W., Silversides D.W., Xu L., and Overbeek P.A. Formation of corneal endothelium is essential for anterior segment development-A transgenic mouse model of anterior segment dysgenesis. Development 127 (2000) 533-542
-
(2000)
Development
, vol.127
, pp. 533-542
-
-
Reneker, L.W.1
Silversides, D.W.2
Xu, L.3
Overbeek, P.A.4
-
52
-
-
3342982949
-
Congenital corneal opacities in a cornea referral practice
-
Rezende R.A., Uchoa U.B., Uchoa R., Rapuano C.J., Laibson P.R., and Cohen E.J. Congenital corneal opacities in a cornea referral practice. Cornea 23 (2004) 565-570
-
(2004)
Cornea
, vol.23
, pp. 565-570
-
-
Rezende, R.A.1
Uchoa, U.B.2
Uchoa, R.3
Rapuano, C.J.4
Laibson, P.R.5
Cohen, E.J.6
-
53
-
-
0035864962
-
A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice
-
Rieger D.K., Reichenberger E., McLean W., Sidow A., and Olsen B.R. A double-deletion mutation in the Pitx3 gene causes arrested lens development in aphakia mice. Genomics 72 (2001) 61-72
-
(2001)
Genomics
, vol.72
, pp. 61-72
-
-
Rieger, D.K.1
Reichenberger, E.2
McLean, W.3
Sidow, A.4
Olsen, B.R.5
-
54
-
-
0037439268
-
Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney
-
Rossi M., Morita H., Sormunen R., Airenne S., Kreivi M., Wang L., Fukai N., Olsen B.R., Tryggvason K., and Soininen R. Heparan sulfate chains of perlecan are indispensable in the lens capsule but not in the kidney. EMBO J. 22 (2003) 236-245
-
(2003)
EMBO J.
, vol.22
, pp. 236-245
-
-
Rossi, M.1
Morita, H.2
Sormunen, R.3
Airenne, S.4
Kreivi, M.5
Wang, L.6
Fukai, N.7
Olsen, B.R.8
Tryggvason, K.9
Soininen, R.10
-
55
-
-
0031811116
-
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
-
Semina E.V., Ferrell R.E., Mintz-Hittner H.A., Bitoun P., Alward W.L., Reiter R.S., Funkhauser C., Daack-Hirsch S., and Murray J.C. A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat. Genet. 19 (1998) 167-170
-
(1998)
Nat. Genet.
, vol.19
, pp. 167-170
-
-
Semina, E.V.1
Ferrell, R.E.2
Mintz-Hittner, H.A.3
Bitoun, P.4
Alward, W.L.5
Reiter, R.S.6
Funkhauser, C.7
Daack-Hirsch, S.8
Murray, J.C.9
-
56
-
-
0034234546
-
Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice
-
Semina E.V., Murray J.C., Reiter R., Hrstka R.F., and Graw J. Deletion in the promoter region and altered expression of Pitx3 homeobox gene in aphakia mice. Hum. Mol. Genet. 9 (2000) 1575-1585
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1575-1585
-
-
Semina, E.V.1
Murray, J.C.2
Reiter, R.3
Hrstka, R.F.4
Graw, J.5
-
57
-
-
0035253581
-
Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts
-
Semina E.V., Brownell I., Mintz-Hittner H.A., Murray J.C., and Jamrich M. Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts. Hum. Mol. Genet. 10 (2001) 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
-
58
-
-
0034641597
-
Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome)
-
Sertie A.L., Sossi V., Camargo A.A., Zatz M., Brahe C., and Passos-Bueno M.R. Collagen XVIII, containing an endogenous inhibitor of angiogenesis and tumor growth, plays a critical role in the maintenance of retinal structure and in neural tube closure (Knobloch syndrome). Hum. Mol. Genet. 9 (2000) 2051-2058
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2051-2058
-
-
Sertie, A.L.1
Sossi, V.2
Camargo, A.A.3
Zatz, M.4
Brahe, C.5
Passos-Bueno, M.R.6
-
59
-
-
15944427842
-
Zebrafish pitx3 is necessary for normal lens and retinal development
-
Shi X., Bosenko D.V., Zinkevich N.S., Foley S., Hyde D.R., Semina E.V., and Vihtelic T.S. Zebrafish pitx3 is necessary for normal lens and retinal development. Mech. Dev. 122 (2005) 513-527
-
(2005)
Mech. Dev.
, vol.122
, pp. 513-527
-
-
Shi, X.1
Bosenko, D.V.2
Zinkevich, N.S.3
Foley, S.4
Hyde, D.R.5
Semina, E.V.6
Vihtelic, T.S.7
-
60
-
-
0028609363
-
Microphthalmia and associated abnormalities in inbred black mice
-
Smith R.S., Roderick T.H., and Sundberg J.P. Microphthalmia and associated abnormalities in inbred black mice. Lab. Anim. Sci. 44 (1994) 551-560
-
(1994)
Lab. Anim. Sci.
, vol.44
, pp. 551-560
-
-
Smith, R.S.1
Roderick, T.H.2
Sundberg, J.P.3
-
61
-
-
23944494639
-
Morphogenesis of the anterior segment in the zebrafish eye
-
Soules K., and Link B. Morphogenesis of the anterior segment in the zebrafish eye. BMC Dev. Biol. 5 (2005) 12
-
(2005)
BMC Dev. Biol.
, vol.5
, pp. 12
-
-
Soules, K.1
Link, B.2
-
62
-
-
12644303220
-
Mutations affecting development of the notochord in zebrafish
-
Stemple D.L., Solnica-Krezel L., Zwartkruis F., Neuhauss S.C., Schier A.F., Malicki J., Stainier D.Y., Abdelilah S., Rangini Z., Mountcastle-Shah E., and Driever W. Mutations affecting development of the notochord in zebrafish. Development 123 (1996) 117-128
-
(1996)
Development
, vol.123
, pp. 117-128
-
-
Stemple, D.L.1
Solnica-Krezel, L.2
Zwartkruis, F.3
Neuhauss, S.C.4
Schier, A.F.5
Malicki, J.6
Stainier, D.Y.7
Abdelilah, S.8
Rangini, Z.9
Mountcastle-Shah, E.10
Driever, W.11
-
63
-
-
3242719404
-
Missense variations in the fibulin 5 gene and age-related macular degeneration
-
Stone E.M., Braun T.A., Russell S.R., Kuehn M.H., Lotery A.J., Moore P.A., Eastman C.G., Casavant T.L., and Sheffield V.C. Missense variations in the fibulin 5 gene and age-related macular degeneration. N. Engl. J. Med. 351 (2004) 346-353
-
(2004)
N. Engl. J. Med.
, vol.351
, pp. 346-353
-
-
Stone, E.M.1
Braun, T.A.2
Russell, S.R.3
Kuehn, M.H.4
Lotery, A.J.5
Moore, P.A.6
Eastman, C.G.7
Casavant, T.L.8
Sheffield, V.C.9
-
64
-
-
0035281572
-
A large-scale in situ screen provides molecular evidence for the induction of eye anterior segment structures by the developing lens
-
Thut C.J., Rountree R.B., Hwa M., and Kingsley D.M. A large-scale in situ screen provides molecular evidence for the induction of eye anterior segment structures by the developing lens. Dev. Biol. 231 (2001) 63-76
-
(2001)
Dev. Biol.
, vol.231
, pp. 63-76
-
-
Thut, C.J.1
Rountree, R.B.2
Hwa, M.3
Kingsley, D.M.4
-
65
-
-
27744515121
-
Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy
-
Van Agtmael T., Schlotzer-Schrehardt U., McKie L., Brownstein D.G., Lee A.W., Cross S.H., Sado Y., Mullins J.J., Poschl E., and Jackson I.J. Dominant mutations of Col4a1 result in basement membrane defects which lead to anterior segment dysgenesis and glomerulopathy. Hum. Mol. Genet. 14 (2005) 3161-3168
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 3161-3168
-
-
Van Agtmael, T.1
Schlotzer-Schrehardt, U.2
McKie, L.3
Brownstein, D.G.4
Lee, A.W.5
Cross, S.H.6
Sado, Y.7
Mullins, J.J.8
Poschl, E.9
Jackson, I.J.10
-
66
-
-
0036177597
-
Zebrafish mutagenesis yields eye morphological mutants with retinal and lens defects
-
Vihtelic T.S., and Hyde D.R. Zebrafish mutagenesis yields eye morphological mutants with retinal and lens defects. Vision Res. 42 (2002) 535-540
-
(2002)
Vision Res.
, vol.42
, pp. 535-540
-
-
Vihtelic, T.S.1
Hyde, D.R.2
-
67
-
-
0035213154
-
Arrested differentiation and epithelial cell degeneration in zebrafish lens mutants
-
Vihtelic T.S., Yamamoto Y., Sweeney M.T., Jeffery W.R., and Hyde D.R. Arrested differentiation and epithelial cell degeneration in zebrafish lens mutants. Dev. Dyn. 222 (2001) 625-636
-
(2001)
Dev. Dyn.
, vol.222
, pp. 625-636
-
-
Vihtelic, T.S.1
Yamamoto, Y.2
Sweeney, M.T.3
Jeffery, W.R.4
Hyde, D.R.5
-
68
-
-
17444377948
-
Lens opacity and photoreceptor degeneration in the zebrafish lens opaque mutant
-
Vihtelic T.S., Yamamoto Y., Springer S.S., Jeffery W.R., and Hyde D.R. Lens opacity and photoreceptor degeneration in the zebrafish lens opaque mutant. Dev. Dyn. 233 (2005) 52-65
-
(2005)
Dev. Dyn.
, vol.233
, pp. 52-65
-
-
Vihtelic, T.S.1
Yamamoto, Y.2
Springer, S.S.3
Jeffery, W.R.4
Hyde, D.R.5
-
69
-
-
0037379295
-
PITs and FOXes in ocular genetics: the Cogan lecture
-
Walter M.A. PITs and FOXes in ocular genetics: the Cogan lecture. Invest. Ophthalmol. Visual Sci. 44 (2003) 1402-1405
-
(2003)
Invest. Ophthalmol. Visual Sci.
, vol.44
, pp. 1402-1405
-
-
Walter, M.A.1
-
71
-
-
21244461514
-
A GFP-based genetic screen reveals mutations that disrupt the architecture of the zebrafish retinotectal projection
-
Xiao T., Roeser T., Staub W., and Baier H. A GFP-based genetic screen reveals mutations that disrupt the architecture of the zebrafish retinotectal projection. Development 132 (2005) 2955-2967
-
(2005)
Development
, vol.132
, pp. 2955-2967
-
-
Xiao, T.1
Roeser, T.2
Staub, W.3
Baier, H.4
-
72
-
-
0642333828
-
Lack of type XVIII collagen results in anterior ocular defects
-
Ylikarppa R., Eklund L., Sormunen R., Kontiola A.I., Utriainen A., Maatta M., Fukai N., Olsen B.R., and Pihlajaniemi T. Lack of type XVIII collagen results in anterior ocular defects. FASEB J. 17 (2003) 2257-2259
-
(2003)
FASEB J.
, vol.17
, pp. 2257-2259
-
-
Ylikarppa, R.1
Eklund, L.2
Sormunen, R.3
Kontiola, A.I.4
Utriainen, A.5
Maatta, M.6
Fukai, N.7
Olsen, B.R.8
Pihlajaniemi, T.9
-
73
-
-
8444221929
-
Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
-
Zenker M., Aigner T., Wendler O., Tralau T., Muntefering H., Fenski R., Pitz S., Schumacher V., Royer-Pokora B., Wuhl E., Cochat P., Bouvier R., Kraus C., Mark K., Madlon H., Dotsch J., Rascher W., Maruniak-Chudek I., Lennert T., Neumann L.M., and Reis A. Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities. Hum. Mol. Genet. 13 (2004) 2625-2632
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 2625-2632
-
-
Zenker, M.1
Aigner, T.2
Wendler, O.3
Tralau, T.4
Muntefering, H.5
Fenski, R.6
Pitz, S.7
Schumacher, V.8
Royer-Pokora, B.9
Wuhl, E.10
Cochat, P.11
Bouvier, R.12
Kraus, C.13
Mark, K.14
Madlon, H.15
Dotsch, J.16
Rascher, W.17
Maruniak-Chudek, I.18
Lennert, T.19
Neumann, L.M.20
Reis, A.21
more..
-
74
-
-
24344432695
-
Demonstration of two novel LAMB2 mutations in the original Pierson syndrome family reported 42 years ago
-
Zenker M., Pierson M., Jonveaux P., and Reis A. Demonstration of two novel LAMB2 mutations in the original Pierson syndrome family reported 42 years ago. Am. J. Med. Genet. A 138 (2005) 73-74
-
(2005)
Am. J. Med. Genet. A
, vol.138
, pp. 73-74
-
-
Zenker, M.1
Pierson, M.2
Jonveaux, P.3
Reis, A.4
-
75
-
-
33646367199
-
Laminin alpha 1 gene is essential for normal lens development in zebrafish
-
Zinkevich N.S., Bosenko D.V., Link B.A., and Semina E.V. Laminin alpha 1 gene is essential for normal lens development in zebrafish. BMC Dev. Biol. 6 (2006) 13
-
(2006)
BMC Dev. Biol.
, vol.6
, pp. 13
-
-
Zinkevich, N.S.1
Bosenko, D.V.2
Link, B.A.3
Semina, E.V.4
|