-
3
-
-
0032563188
-
Protein kinase C regulates chondrogenesis of mesenchymes via mitogen-activated protein kinase signaling
-
Chang S. H., Oh C. D., Yang M. S., Kang S. S., Lee Y. S., Sonn J. K., Chun J. S. Protein kinase C regulates chondrogenesis of mesenchymes via mitogen-activated protein kinase signaling. J. Biol. Chem. 273:1998;19213-19219.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 19213-19219
-
-
Chang, S.H.1
Oh, C.D.2
Yang, M.S.3
Kang, S.S.4
Lee, Y.S.5
Sonn, J.K.6
Chun, J.S.7
-
4
-
-
0001912623
-
Lens development. The role of the lens in eye growth
-
Coulombre A. J., Coulombre J. L. Lens development. The role of the lens in eye growth. J. Exp. Zool. 156:1964;39-48.
-
(1964)
J. Exp. Zool.
, vol.156
, pp. 39-48
-
-
Coulombre, A.J.1
Coulombre, J.L.2
-
5
-
-
0345092879
-
Physiology
-
G. Smolin, & R. A. Thoft. Boston: Little, Brown
-
Edelhauser H. F., Geroski D. H., Ubels J. L. Physiology. Smolin G., Thoft R. A. The Cornea. 1994;25-46 Little, Brown, Boston.
-
(1994)
The Cornea
, pp. 25-46
-
-
Edelhauser, H.F.1
Geroski, D.H.2
Ubels, J.L.3
-
6
-
-
0030844354
-
Bone morphogenetic proteins (BMPs) as regulators of dorsal forebrain development
-
Furuta Y., Piston D. W., Hogan B. L. M. Bone morphogenetic proteins (BMPs) as regulators of dorsal forebrain development. Development. 124:1997;2203-2212.
-
(1997)
Development
, vol.124
, pp. 2203-2212
-
-
Furuta, Y.1
Piston, D.W.2
Hogan, B.L.M.3
-
7
-
-
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
-
8
-
-
0014035180
-
Causal factors in corneal development: An experimental analysis in the chick embryo
-
Genis-Galvez J. M., Santos-Gutierrez L., Rios-Gonzalez A. Causal factors in corneal development: An experimental analysis in the chick embryo. Exp. Eye Res. 6:1967;48-56.
-
(1967)
Exp. Eye Res.
, vol.6
, pp. 48-56
-
-
Genis-Galvez, J.M.1
Santos-Gutierrez, L.2
Rios-Gonzalez, A.3
-
9
-
-
0003290037
-
Congenital hydrocephalus in the mouse, a case of spurious pleiotropism
-
Gruneberg H. Congenital hydrocephalus in the mouse, a case of spurious pleiotropism. J. Genet. 45:1943;1-21.
-
(1943)
J. Genet.
, vol.45
, pp. 1-21
-
-
Gruneberg, H.1
-
10
-
-
0030056968
-
Cell adhesion: The molecular basis of tissue architecture and morphogenesis
-
Gumbiner B. M. Cell adhesion: The molecular basis of tissue architecture and morphogenesis. Cell. 84:1996;345-357.
-
(1996)
Cell
, vol.84
, pp. 345-357
-
-
Gumbiner, B.M.1
-
11
-
-
0021066058
-
On the ultrastructure of the developing and adult mouse corneal stroma
-
Haustein J. On the ultrastructure of the developing and adult mouse corneal stroma. Anat. Embryol. 168:1983;291-305.
-
(1983)
Anat. Embryol.
, vol.168
, pp. 291-305
-
-
Haustein, J.1
-
12
-
-
0019306591
-
Development of the vertebrate cornea
-
Hay E. D. Development of the vertebrate cornea. Int. Rev. Cytol. 63:1979;263-322.
-
(1979)
Int. Rev. Cytol.
, vol.63
, pp. 263-322
-
-
Hay, E.D.1
-
13
-
-
0014611096
-
Fine structure of the developing avian cornea
-
Hay E. D., Revel J. P. Fine structure of the developing avian cornea. Monogr. Dev. Biol. 1:1969;1-144.
-
(1969)
Monogr. Dev. Biol.
, vol.1
, pp. 1-144
-
-
Hay, E.D.1
Revel, J.P.2
-
15
-
-
0033041178
-
Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcription factor gene
-
Hong H.-K., Lass J. H., Chakravarti A. Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcription factor gene. Hum. Mol. Genet. 8:1999;625-637.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 625-637
-
-
Hong, H.-K.1
Lass, J.H.2
Chakravarti, A.3
-
16
-
-
0023128462
-
Congenital hereditary corneal oedema of Maumenee: Its clinical features, management and pathology
-
Kirkness C. M., McCartney A., Rice N. S. C., Garner A., Steele A. D. M. Congenital hereditary corneal oedema of Maumenee: Its clinical features, management and pathology. Br. J. Ophthalmol. 71:1987;130-144.
-
(1987)
Br. J. Ophthalmol.
, vol.71
, pp. 130-144
-
-
Kirkness, C.M.1
McCartney, A.2
Rice, N.S.C.3
Garner, A.4
Steele, A.D.M.5
-
17
-
-
0032511231
-
The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus
-
Kume T., Deng K. Y., Winfrey V., Gould D. B., Walter M. A., Hogan B. L. The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus. Cell. 93:1998;985-996.
-
(1998)
Cell
, vol.93
, pp. 985-996
-
-
Kume, T.1
Deng, K.Y.2
Winfrey, V.3
Gould, D.B.4
Walter, M.A.5
Hogan, B.L.6
-
18
-
-
0032231330
-
Mutations of the forkhead/winged helix gene, FREAC3, in patients with glaucoma and anterior segment dysgenesis
-
Mears A. J., Jordan T., Mirzayans F., Dubois S., Kume T., Parlee M., Ritch R., Koop B., Kuo W.-L., Collins C., Marshall J., Gould D. B., Pearce W., Carlsson P., Enerback S., Morissette J., Battacharya S., Hogan B., Raymond V., Walter M. A. Mutations of the forkhead/winged helix gene, FREAC3, in patients with glaucoma and anterior segment dysgenesis. Am. J. Hum. Genet. 63:1998;1316-1328.
-
(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
Battacharya, S.17
Hogan, B.18
Raymond, V.19
Walter, M.A.20
more..
-
19
-
-
0029807866
-
Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25
-
Mears A. J., Mirzayans F., Gould D. B., Pearce W. G., Walter M. A. Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25. Am. J. Hum. Genet. 59:1996;1321-1327.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 1321-1327
-
-
Mears, A.J.1
Mirzayans, F.2
Gould, D.B.3
Pearce, W.G.4
Walter, M.A.5
-
20
-
-
85029463873
-
-
Submitted for publication
-
Mirzayans, F, Gould, D. B, Heon, E, Billingsley, G. D, Cheung, J. C, Mears, A. J, and, Walter, M. A. 1999, Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25. Submitted for publication.
-
(1999)
Axenfeld-Rieger Syndrome Resulting from Mutation of the FKHL7 Gene on Chromosome 6p25
-
-
Mirzayans, F.1
Gould, D.B.2
Heon, E.3
Billingsley, G.D.4
Cheung, J.C.5
Mears, A.J.6
Walter, M.A.7
-
21
-
-
0026663734
-
A PDGF receptor mutation in the mouse (Patch) perturbs the development of a non-neuronal subset of neural crest-derived cells
-
Morrison-Graham K., Schatteman G. C., Bork T., Bowen-Pope D. F., Weston J. A. A PDGF receptor mutation in the mouse (Patch) perturbs the development of a non-neuronal subset of neural crest-derived cells. Development. 115:1992;133-142.
-
(1992)
Development
, vol.115
, pp. 133-142
-
-
Morrison-Graham, K.1
Schatteman, G.C.2
Bork, T.3
Bowen-Pope, D.F.4
Weston, J.A.5
-
22
-
-
0028838036
-
Congenital hereditary endothelial dystrophy associated with glaucoma
-
Mullaney P. B., Risco J. M., Teichmann K., Millar L. Congenital hereditary endothelial dystrophy associated with glaucoma. Ophthalmology. 102:1995;186-192.
-
(1995)
Ophthalmology
, vol.102
, pp. 186-192
-
-
Mullaney, P.B.1
Risco, J.M.2
Teichmann, K.3
Millar, L.4
-
23
-
-
17344368672
-
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
-
Nishimura D. Y., Swiderski R. E., Alward W. L., Searby C. C., Patil S. R., Bennet S. R., Kanis A. B., Gastier J. M., Stone E. M., Sheffield V. C. The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nat. Genet. 19:1998;140-147.
-
(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
-
24
-
-
0028107165
-
Expression and functional involvement of N-cadherin in embryonic limb chondrogenesis
-
Oberlender S. A., Tuan R. S. Expression and functional involvement of N-cadherin in embryonic limb chondrogenesis. Development. 120:1994;177-187.
-
(1994)
Development
, vol.120
, pp. 177-187
-
-
Oberlender, S.A.1
Tuan, R.S.2
-
25
-
-
0015149369
-
Electron microscopic study of the development of the mouse corneal endothelium
-
Pei Y. F., Rhodin J. A. Electron microscopic study of the development of the mouse corneal endothelium. Invest. Opthalmol. 10:1971;811-825.
-
(1971)
Invest. Opthalmol.
, vol.10
, pp. 811-825
-
-
Pei, Y.F.1
Rhodin, J.A.2
-
26
-
-
0030589515
-
Lens-specific expression of PDGF-A alters lens growth and development
-
Reneker L. W., Overbeek P. A. Lens-specific expression of PDGF-A alters lens growth and development. Dev. Biol. 180:1996;554-565.
-
(1996)
Dev. Biol.
, vol.180
, pp. 554-565
-
-
Reneker, L.W.1
Overbeek, P.A.2
-
27
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
Semina E. V., Reiter R., Leysens N. J., Alward W. L. M., Small K. W., Datson N. A., Siegel-Bartelt J., Bierke-Nelson D., Bitoun P., Zabel B. U., Carey J. C., Murray J. C. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat. Genet. 14:1996;392-399.
-
(1996)
Nat. Genet.
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Alward, W.L.M.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
-
29
-
-
0023030826
-
Identification of ZO-1: A high molecular weight polypeptide associated with the tight junction (zonula occludens) in a variety of epithelia
-
Stevenson B. R., Siliciano J. D., Mooseker M. S., Goodenough D. A. Identification of ZO-1: A high molecular weight polypeptide associated with the tight junction (zonula occludens) in a variety of epithelia. J. Cell Biol. 103:1986;755-766.
-
(1986)
J. Cell Biol.
, vol.103
, pp. 755-766
-
-
Stevenson, B.R.1
Siliciano, J.D.2
Mooseker, M.S.3
Goodenough, D.A.4
-
30
-
-
0023926935
-
The cadherins: Cell-cell adhesion molecules controlling animal morphogenesis
-
Takeichi M. The cadherins: Cell-cell adhesion molecules controlling animal morphogenesis. Development. 102:1988;639-655.
-
(1988)
Development
, vol.102
, pp. 639-655
-
-
Takeichi, M.1
-
31
-
-
0027962501
-
N-CAM and N-cadherin expression during in vitro chondrogenesis
-
Tavella S., Raffo P., Tacchetti C., Cancedda R., Castognola P. N-CAM and N-cadherin expression during in vitro chondrogenesis. Exp. Cell Res. 215:1994;354-362.
-
(1994)
Exp. Cell Res.
, vol.215
, pp. 354-362
-
-
Tavella, S.1
Raffo, P.2
Tacchetti, C.3
Cancedda, R.4
Castognola, P.5
|