-
1
-
-
0029682036
-
Eye ancestry: Old genes for new eyes
-
Nilsson DE. Eye ancestry: old genes for new eyes. Curr Biol 1996: 6: 39-42.
-
(1996)
Curr Biol
, vol.6
, pp. 39-42
-
-
Nilsson, D.E.1
-
2
-
-
0030987235
-
Pax-6: Where to be conserved is not conservative
-
Harris WA. Pax-6: where to be conserved is not conservative. Proc Natl Acad Sci USA 1997: 94: 2098-2100.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 2098-2100
-
-
Harris, W.A.1
-
3
-
-
0026345992
-
Mouse small eye results from mutations in a paired-like homeobox-containing gene
-
Hill RE, Favor J, Hogan BL, Ton CC, Saunders GF, Hanson IM, Prosser J, Jordan T, Hastie ND, van Heyningen V. Mouse small eye results from mutations in a paired-like homeobox-containing gene. Nature 1991: 354: 522-525.
-
(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
-
4
-
-
0026907123
-
The human PAX6 gene is mutated in two patients with aniridia
-
Jordan T, Hanson I, Zaletayev D, Hodgson S, Prosser J, Seawright A, Hastie N, van Heyningen V. The human PAX6 gene is mutated in two patients with aniridia. Nat Genet 1992: 1: 328-332.
-
(1992)
Nat Genet
, vol.1
, pp. 328-332
-
-
Jordan, T.1
Hanson, I.2
Zaletayev, D.3
Hodgson, S.4
Prosser, J.5
Seawright, A.6
Hastie, N.7
Van Heyningen, V.8
-
5
-
-
0027965633
-
Homolgy of the eyeless gene of Drosphila to the Small eye gene in mice and Aniridia in humans
-
Quiring R, Waldorf U, Kloter U, Gehring WJ. Homolgy of the eyeless gene of Drosphila to the Small eye gene in mice and Aniridia in humans. Science 1994: 265: 785-789.
-
(1994)
Science
, vol.265
, pp. 785-789
-
-
Quiring, R.1
Waldorf, U.2
Kloter, U.3
Gehring, W.J.4
-
6
-
-
0031459431
-
Eye development: Governed by a dictator or a junta?
-
Desplan C. Eye development: governed by a dictator or a junta? Cell 1997: 91: 861-864.
-
(1997)
Cell
, vol.91
, pp. 861-864
-
-
Desplan, C.1
-
7
-
-
0030864934
-
Transcription factors in eye development: A gorgeous mosaic?
-
Kumar J, Moses K. Transcription factors in eye development: a gorgeous mosaic? Genes Dev 1997: 11: 2023-2028.
-
(1997)
Genes Dev
, vol.11
, pp. 2023-2028
-
-
Kumar, J.1
Moses, K.2
-
8
-
-
0027953771
-
Hox genes in vertebrate development
-
Krumlauf R. Hox genes in vertebrate development. Cell 1994: 78: 191-201.
-
(1994)
Cell
, vol.78
, pp. 191-201
-
-
Krumlauf, R.1
-
9
-
-
0031745167
-
Limb development: Molecular dysmorphology is at hand!
-
Innis JW, Mortlock DP. Limb development: molecular dysmorphology is at hand!. Clin Genet 1998: 53: 337-348.
-
(1998)
Clin Genet
, vol.53
, pp. 337-348
-
-
Innis, J.W.1
Mortlock, D.P.2
-
10
-
-
0029929286
-
Genetic aspects of embryonic eye development in vertevbrates
-
Graw J. Genetic aspects of embryonic eye development in vertevbrates. Dev Genet 1996: 18: 181-197.
-
(1996)
Dev Genet
, vol.18
, pp. 181-197
-
-
Graw, J.1
-
12
-
-
0030031201
-
Cell fate determination in the vertebrate retina
-
Cepko CL, Austin CP, Yang XY, Alexiades M, Ezzedine D. Cell fate determination in the vertebrate retina. Proc Natl Acad Sci USA 1996: 93: 589-595.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 589-595
-
-
Cepko, C.L.1
Austin, C.P.2
Yang, X.Y.3
Alexiades, M.4
Ezzedine, D.5
-
13
-
-
0030218097
-
The patterning and onset of opsin expression in vertebrate retinae
-
Cepko CL. The patterning and onset of opsin expression in vertebrate retinae. Curr Opin Neurobiol 1996: 6: 542-546.
-
(1996)
Curr Opin Neurobiol
, vol.6
, pp. 542-546
-
-
Cepko, C.L.1
-
14
-
-
0030813163
-
Identification of genes causing photoreceptor degenerations leading to blindness
-
Farber DB, Danciger M. Identification of genes causing photoreceptor degenerations leading to blindness. Curr Opin Neurobiol 1997: 7: 666-673.
-
(1997)
Curr Opin Neurobiol
, vol.7
, pp. 666-673
-
-
Farber, D.B.1
Danciger, M.2
-
15
-
-
0030802112
-
Defining intermediate stages in cell determination: Acquisition of a lens-forming bias in head ectoderm during lends determination
-
Grainger RM, Mannion JE, Cook TLJ, Zygar CA. Defining intermediate stages in cell determination: acquisition of a lens-forming bias in head ectoderm during lends determination. Dev Genet 1997: 20: 246-257.
-
(1997)
Dev Genet
, vol.20
, pp. 246-257
-
-
Grainger, R.M.1
Mannion, J.E.2
Cook, T.L.J.3
Zygar, C.A.4
-
16
-
-
0029730560
-
Cellular and molecular features of lens differentiation: A review of recent advances
-
Wride MA. Cellular and molecular features of lens differentiation: a review of recent advances. Differentiation 1996: 61: 77-93.
-
(1996)
Differentiation
, vol.61
, pp. 77-93
-
-
Wride, M.A.1
-
17
-
-
0030051943
-
The biology of vision in Drosphila
-
Zuker CS. The biology of vision in Drosphila. Proc Natl Acad Sci USA 1996: 93: 571-576.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 571-576
-
-
Zuker, C.S.1
-
18
-
-
0020043627
-
Variable expressivity of autosomal dominant anterior segment mesenchymal dysgenesis in six generations
-
Hittner HM, Kretzer FL, Antoszyk JH, Ferrell RE, Mehta RS. Variable expressivity of autosomal dominant anterior segment mesenchymal dysgenesis in six generations. Am J Opthhalmol 1982: 93: 57-70.
-
(1982)
Am J Opthhalmol
, vol.93
, pp. 57-70
-
-
Hittner, H.M.1
Kretzer, F.L.2
Antoszyk, J.H.3
Ferrell, R.E.4
Mehta, R.S.5
-
19
-
-
0018855662
-
Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria
-
Hittner HM, Riccardi VM, Ferrell RE, Borda RR, Justice JJ. Variable expressivity in autosomal dominant aniridia by clinical, electrophysiologic, and angiographic criteria. Am J Opthalmol 1908: 89: 531-539.
-
(1908)
Am J Opthalmol
, vol.89
, pp. 531-539
-
-
Hittner, H.M.1
Riccardi, V.M.2
Ferrell, R.E.3
Borda, R.R.4
Justice, J.J.5
-
20
-
-
0031473505
-
Genomes and evolution postgenome, pre-chromosome
-
Ashburner M, Maizels N. Genomes and evolution postgenome, pre-chromosome. Curr Opin Genet Dev 1997: 7: 747-749.
-
(1997)
Curr Opin Genet Dev
, vol.7
, pp. 747-749
-
-
Ashburner, M.1
Maizels, N.2
-
22
-
-
0027521076
-
The rise and fall of positional cloning?
-
Ballabio A. The rise and fall of positional cloning? Nat Genet 1993: 3: 277-279.
-
(1993)
Nat Genet
, vol.3
, pp. 277-279
-
-
Ballabio, A.1
-
23
-
-
0031574611
-
Molecular fish on chips
-
Goffeau A. Molecular fish on chips. Nature 1997: 385: 202-203.
-
(1997)
Nature
, vol.385
, pp. 202-203
-
-
Goffeau, A.1
-
24
-
-
0026949405
-
Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
-
Glaser T, Walton DS, Maas RL. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene. Nat Genet 1992: 2: 232-239.
-
(1992)
Nat Genet
, vol.2
, pp. 232-239
-
-
Glaser, T.1
Walton, D.S.2
Maas, R.L.3
-
25
-
-
0026315044
-
Positional cloning and characterization of a paired box-and homebox-containing gene from the aniridia region
-
Ton CC, Hirvonen H, Miwa H, Weil MM, Monaghan P, Jordan T, van Heyningen V, Hastie ND, Meijiers-Heijboer H, Drechsler M. Positional cloning and characterization of a paired box-and homebox-containing gene from the aniridia region. Cell 1991: 67: 1059-1074.
-
(1991)
Cell
, vol.67
, pp. 1059-1074
-
-
Ton, C.C.1
Hirvonen, H.2
Miwa, H.3
Weil, M.M.4
Monaghan, P.5
Jordan, T.6
Van Heyningen, V.7
Hastie, N.D.8
Meijiers-Heijboer, H.9
Drechsler, M.10
-
26
-
-
10544233785
-
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome
-
Semina EV, Reiter R, Leysens NJ, Alward WL, Small KW, Datson NA, Siegel-Bartelt J, Bierke-Nelson D, Bitoun P, Zabel BU, Carey JC, Murray JC. Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet 1996: 14: 392-399.
-
(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
-
27
-
-
0031811116
-
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
-
Semina EV, Ferrell RE, Mintz-Hittner HA, Bitoun P, Alward WL, Reiter RS, Funkhauser C, Daack-Hirsch S, Murray JC. A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD. Nat Genet 1998: 19: 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
-
28
-
-
17344368672
-
The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25
-
Nishimura DY, Swiderski RE, Alward WL, Searby CC, Patil SR, Bennet SR, Kanis AB, Gastier JM, Stone EM, Sheffield VC. The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25. Nat Genet 1998: 19: 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
-
31
-
-
15144352798
-
-
http://www.hgu.mrc.ac.uk/Softdata/PAX6/
-
-
-
-
32
-
-
0030581164
-
Influence of PAX6 gene dosage on development: Overexpression causes severe eye abnormalities
-
Schedl A, Ross A, Lee M, Engelkamp D, Rashbass P, van Heyningen V, Hastie ND. Influence of PAX6 gene dosage on development: overexpression causes severe eye abnormalities. Cell 1996: 86: 71-82.
-
(1996)
Cell
, vol.86
, pp. 71-82
-
-
Schedl, A.1
Ross, A.2
Lee, M.3
Engelkamp, D.4
Rashbass, P.5
Van Heyningen, V.6
Hastie, N.D.7
-
33
-
-
0028074973
-
PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anotpthalmia and central nervous system defects
-
Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, Maas RL. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anotpthalmia and central nervous system defects. Nat Genet 1994: 7: 463-471.
-
(1994)
Nat Genet
, vol.7
, pp. 463-471
-
-
Glaser, T.1
Jepeal, L.2
Edwards, J.G.3
Young, S.R.4
Favor, J.5
Maas, R.L.6
-
34
-
-
0032511231
-
The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus
-
Kume T, Deng KY, Winfrey V, Gould DB, Walter MA, Hogan BL. The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus. Cell 1998: 93: 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
-
35
-
-
0030669568
-
Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gen (CRX) essential for maintenance fo the photoreceptor
-
Freund CL, Gregorh-Evans CY, Furukawa T, Papaioannou M, Looser J, Ploder L, Bellingham J, Ng D, Herbrick JA, Duncan A, Scherer SW, Tsui LC, Loutradis-Anagnostou A, Jacobson SG, Cepko CL, Bhattacharya SS, McInnes RR. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gen (CRX) essential for maintenance fo the photoreceptor. Cell 1997: 91: 543-553.
-
(1997)
Cell
, vol.91
, pp. 543-553
-
-
Freund, C.L.1
Gregorh-Evans, C.Y.2
Furukawa, T.3
Papaioannou, M.4
Looser, J.5
Ploder, L.6
Bellingham, J.7
Ng, D.8
Herbrick, J.A.9
Duncan, A.10
Scherer, S.W.11
Tsui, L.C.12
Loutradis-Anagnostou, A.13
Jacobson, S.G.14
Cepko, C.L.15
Bhattacharya, S.S.16
McInnes, R.R.17
-
36
-
-
0030725687
-
Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation
-
Furukawa T, Morrow EM, Cepko CL. Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation. Cell 1997: 91: 531-541.
-
(1997)
Cell
, vol.91
, pp. 531-541
-
-
Furukawa, T.1
Morrow, E.M.2
Cepko, C.L.3
-
37
-
-
0030781996
-
Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes
-
Chen S, Wang QL, Nie Z, Sun H, Lennon G, Copeland NG, Gilbert DJ, Jenkins NA, Zack DJ. Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes. Neuron 1997: 19: 1017-1030.
-
(1997)
Neuron
, vol.19
, pp. 1017-1030
-
-
Chen, S.1
Wang, Q.L.2
Nie, Z.3
Sun, H.4
Lennon, G.5
Copeland, N.G.6
Gilbert, D.J.7
Jenkins, N.A.8
Zack, D.J.9
-
38
-
-
0345367079
-
Mutations in the retinal guanylate cyclast (RETGC-1) gene in dominant cone-rod dystrophy
-
Kelsell RE, Gregory-Evans K, Payne AM, Perrault I, Kaplan J, Yang RB, Garbers DL, Bird AC, Moore AT, Hunt DM. Mutations in the retinal guanylate cyclast (RETGC-1) gene in dominant cone-rod dystrophy. Hum Mol Genet 1998: 7: 1179-1184.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1179-1184
-
-
Kelsell, R.E.1
Gregory-Evans, K.2
Payne, A.M.3
Perrault, I.4
Kaplan, J.5
Yang, R.B.6
Garbers, D.L.7
Bird, A.C.8
Moore, A.T.9
Hunt, D.M.10
-
39
-
-
16144363583
-
Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis
-
Perrault I, Rozet JM, Calvas P, Gerber S, Camuzat A, Dollfus H, Chatelin S, Souied E, Ghazi I, Leowski C, Bonnemaison M, Le PD, Frezal J, DuFier JL, Pittler S, Munnich A, Kaplan J. Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis. Nat Genet 1996: 14: 461-464.
-
(1996)
Nat Genet
, vol.14
, pp. 461-464
-
-
Perrault, I.1
Rozet, J.M.2
Calvas, P.3
Gerber, S.4
Camuzat, A.5
Dollfus, H.6
Chatelin, S.7
Souied, E.8
Ghazi, I.9
Leowski, C.10
Bonnemaison, M.11
Le, P.D.12
Frezal, J.13
DuFier, J.L.14
Pittler, S.15
Munnich, A.16
Kaplan, J.17
-
40
-
-
0027447531
-
Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy
-
Wells J, Wroblewski J, Keen J, Inglehearn C, Jubb C, Eckestein A, Jay M, Arden G, Bhattacharya S, Fitzke F. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet 1993: 3: 213-218.
-
(1993)
Nat Genet
, vol.3
, pp. 213-218
-
-
Wells, J.1
Wroblewski, J.2
Keen, J.3
Inglehearn, C.4
Jubb, C.5
Eckestein, A.6
Jay, M.7
Arden, G.8
Bhattacharya, S.9
Fitzke, F.10
-
41
-
-
0032539851
-
Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis
-
Morimura H, Fishman GA, Grover SA, Fulton AB, Berson EL, Dryja TP. Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or Leber congenital amaurosis. Proc Natl Acad Sci USA 1998: 95: 3088-3093.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 3088-3093
-
-
Morimura, H.1
Fishman, G.A.2
Grover, S.A.3
Fulton, A.B.4
Berson, E.L.5
Dryja, T.P.6
-
42
-
-
0032037626
-
De novo mutation in CRX homeobox gene associated with Leber congenital amaurosis
-
Freund CL, Wang QL, Chen S, Muskat BL, Wiles CD, Sheffield VC, Jacobson SG, McInnes RR, Zack DJ, Stone EM. De novo mutation in CRX homeobox gene associated with Leber congenital amaurosis. Nat Genet 1998: 18: 311-312.
-
(1998)
Nat Genet
, vol.18
, pp. 311-312
-
-
Freund, C.L.1
Wang, Q.L.2
Chen, S.3
Muskat, B.L.4
Wiles, C.D.5
Sheffield, V.C.6
Jacobson, S.G.7
McInnes, R.R.8
Zack, D.J.9
Stone, E.M.10
-
43
-
-
0031252434
-
Mutations in RPE65 cause Leber's congenital amaurosis
-
Marlhens F, Bareil C, Griffoin JM, Zrenner E, Amalric P, Eliaou C, Liu SY, Harris E, Redmond TM, Arnaud B, Claustres M, Hamel CP. Mutations in RPE65 cause Leber's congenital amaurosis. Nat Genet 1997: 17: 139-141.
-
(1997)
Nat Genet
, vol.17
, pp. 139-141
-
-
Marlhens, F.1
Bareil, C.2
Griffoin, J.M.3
Zrenner, E.4
Amalric, P.5
Eliaou, C.6
Liu, S.Y.7
Harris, E.8
Redmond, T.M.9
Arnaud, B.10
Claustres, M.11
Hamel, C.P.12
-
44
-
-
0025125431
-
Spatially and temporally restricted expression of the Pax2 during murine neurogenesis
-
Nornes HO, Dressier GR, Knapik EW, Deutsch U, Gruss P. Spatially and temporally restricted expression of the Pax2 during murine neurogenesis. Development 1990: 109: 797-809.
-
(1990)
Development
, vol.109
, pp. 797-809
-
-
Nornes, H.O.1
Dressier, G.R.2
Knapik, E.W.3
Deutsch, U.4
Gruss, P.5
-
45
-
-
0029953417
-
Pax2 contributes to inner ear patterning and optic nerve trajectory
-
Torres M, Gomez-Pardo E, Gruss P. Pax2 contributes to inner ear patterning and optic nerve trajectory. Development 1996: 122: 3381-3391.
-
(1996)
Development
, vol.122
, pp. 3381-3391
-
-
Torres, M.1
Gomez-Pardo, E.2
Gruss, P.3
-
46
-
-
0028884763
-
Mutation of PAX2 in two siblings with rena-coloborna syndrome
-
Sanyanusin P, McNoe LA, Sullivan MJ, Waver RG, Eccles MR. Mutation of PAX2 in two siblings with rena-coloborna syndrome. Hum Mol Genet 1995: 4: 2183-2184.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2183-2184
-
-
Sanyanusin, P.1
McNoe, L.A.2
Sullivan, M.J.3
Waver, R.G.4
Eccles, M.R.5
-
47
-
-
0028966947
-
Mutation of the PAX2 gene in a family with optice nerve colobomas, renal anomalies and vesicoureteral reflux
-
Sanyanusin P, Schimmenti LA, McNoe LA, Ward TA, pierpont ME, Sullivan MJ, Dobyns WB, Eccles MR. Mutation of the PAX2 gene in a family with optice nerve colobomas, renal anomalies and vesicoureteral reflux. Nat Genet 1995: 9: 358-364.
-
(1995)
Nat Genet
, vol.9
, pp. 358-364
-
-
Sanyanusin, P.1
Schimmenti, L.A.2
McNoe, L.A.3
Ward, T.A.4
Pierpont, M.E.5
Sullivan, M.J.6
Dobyns, W.B.7
Eccles, M.R.8
-
48
-
-
16944366271
-
Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations
-
Schimmenti LA, Cunliffe HE, McNoe LA, Ward TA, French MC, Shim HH, Zhang YH, Proesmans W, Leys A, Byerly KA, Braddock SR, Masuno M, Imaizumi K, Devriendt K, Eccles MR. Further delineation of renal-coloboma syndrome in patients with extreme variability of phenotype and identical PAX2 mutations. Am J Hurn Genet 1997: 60: 869-878.
-
(1997)
Am J Hurn Genet
, vol.60
, pp. 869-878
-
-
Schimmenti, L.A.1
Cunliffe, H.E.2
McNoe, L.A.3
Ward, T.A.4
French, M.C.5
Shim, H.H.6
Zhang, Y.H.7
Proesmans, W.8
Leys, A.9
Byerly, K.A.10
Braddock, S.R.11
Masuno, M.12
Imaizumi, K.13
Devriendt, K.14
Eccles, M.R.15
-
49
-
-
0028101943
-
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus
-
Keller SA, Jones JM, Boyle A, Barrow LL, Killen PD, Green DG, Kapousta NV, Hitchcock PF, Swank RT, Meisler MH. Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics 1994: 23: 309-320.
-
(1994)
Genomics
, vol.23
, pp. 309-320
-
-
Keller, S.A.1
Jones, J.M.2
Boyle, A.3
Barrow, L.L.4
Killen, P.D.5
Green, D.G.6
Kapousta, N.V.7
Hitchcock, P.F.8
Swank, R.T.9
Meisler, M.H.10
-
50
-
-
17344362762
-
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in hyman and mouse
-
Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Marensson IL, Toresson H, Fox M, Wales JK, Hindmarsh PC, Krauss S, Beddington RS, Robinson IC. Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in hyman and mouse. Nat Genet 1998: 19: 125-133.
-
(1998)
Nat Genet
, vol.19
, pp. 125-133
-
-
Dattani, M.T.1
Martinez-Barbera, J.P.2
Thomas, P.Q.3
Brickman, J.M.4
Gupta, R.5
Marensson, I.L.6
Toresson, H.7
Fox, M.8
Wales, J.K.9
Hindmarsh, P.C.10
Krauss, S.11
Beddington, R.S.12
Robinson, I.C.13
-
51
-
-
0028356007
-
PAX3 gene structure and mutations: Close analogies between Waardenburg syndrome and the Splotch mouse
-
Tassabehji M, Newton VE, Leverton K, Turnbull K, Seemanova E, Kunze J, Sperling K, Strachan T, Read AP. PAX3 gene structure and mutations: close analogies between Waardenburg syndrome and the Splotch mouse. Hum Mol Genet 1994: 3: 1069-1074.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1069-1074
-
-
Tassabehji, M.1
Newton, V.E.2
Leverton, K.3
Turnbull, K.4
Seemanova, E.5
Kunze, J.6
Sperling, K.7
Strachan, T.8
Read, A.P.9
-
52
-
-
0027518348
-
Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2
-
Tassabehji M, Read AP, Newton VE, Patton M, Gruss P, Harris R, Strachan T, Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2. Nat Genet 1993: 3: 26-30.
-
(1993)
Nat Genet
, vol.3
, pp. 26-30
-
-
Tassabehji, M.1
Read, A.P.2
Newton, V.E.3
Patton, M.4
Gruss, P.5
Harris, R.6
Strachan, T.7
-
53
-
-
0031923931
-
Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7
-
Gary ML, Friedman TB, Asher JHJ, Innis JW. Septo-optic dysplasia and WS1 in the proband of a WS1 family segregating for a novel mutation in PAX3 exon 7. J Med Genet 1998: 35: 248-250.
-
(1998)
J Med Genet
, vol.35
, pp. 248-250
-
-
Gary, M.L.1
Friedman, T.B.2
Asher, J.H.J.3
Innis, J.W.4
-
54
-
-
0028908831
-
Waardenburg syndrome type II: Phenotypic findings and diagnostic criteria
-
Liu XZ, Newton VE, Read AP. Waardenburg syndrome type II: phenotypic findings and diagnostic criteria. Am J Med Genet 1995: 55: 95-100.
-
(1995)
Am J Med Genet
, vol.55
, pp. 95-100
-
-
Liu, X.Z.1
Newton, V.E.2
Read, A.P.3
-
55
-
-
0027943189
-
Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene
-
Tassabhji M, Newton VE, Read AP. Waardenburg syndrome type 2 caused by mutations in the human microphthalmia (MITF) gene. Nat Genet 1994: 8: 251-255.
-
(1994)
Nat Genet
, vol.8
, pp. 251-255
-
-
Tassabhji, M.1
Newton, V.E.2
Read, A.P.3
-
56
-
-
0027204149
-
Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein
-
Hodgkinson CA, Moore KJ, Nakayama A, Steingrimsson E, Copeland NG, Jenkins NA, Arnheeter H. Mutations at the mouse microphthalmia locus are associated with defects in a gene encoding a novel basic-helix-loop-helix-zipper protein. Cell 1993: 74: 395-404.
-
(1993)
Cell
, vol.74
, pp. 395-404
-
-
Hodgkinson, C.A.1
Moore, K.J.2
Nakayama, A.3
Steingrimsson, E.4
Copeland, N.G.5
Jenkins, N.A.6
Arnheeter, H.7
-
57
-
-
10544249464
-
The semidominant Mi(b) mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerization
-
Steingrimsson E, Nii A, Fisher DE, Ferre-D'Amare AR, McCormick FJ, Russell LB, Burley SK, Ward JM, Jenkins NA, Copeland NG. The semidominant Mi(b) mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerization. EMBO J 1996: 15: 6280-6289.
-
(1996)
EMBO J
, vol.15
, pp. 6280-6289
-
-
Steingrimsson, E.1
Nii, A.2
Fisher, D.E.3
Ferre-D'Amare, A.R.4
McCormick, F.J.5
Russell, L.B.6
Burley, S.K.7
Ward, J.M.8
Jenkins, N.A.9
Copeland, N.G.10
-
58
-
-
0030914459
-
Mutations in the human Jagged 1 gene are responsible for Alagille syndrome
-
Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, Piccoll DA, Meltzer PS, Spinner NB, Collins FS, Chandrasekharappa SC. Mutations in the human Jagged 1 gene are responsible for Alagille syndrome. Nat Genet 1997: 16: 235-242.
-
(1997)
Nat Genet
, vol.16
, pp. 235-242
-
-
Oda, T.1
Elkahloun, A.G.2
Pike, B.L.3
Okajima, K.4
Krantz, I.D.5
Genin, A.6
Piccoll, D.A.7
Meltzer, P.S.8
Spinner, N.B.9
Collins, F.S.10
Chandrasekharappa, S.C.11
-
59
-
-
0038875342
-
Alagille syndrome is caused by mutations in human Jagged 1, which encodes a ligand for Notch 1
-
Li L, Krantz ID, Deng Y, Genin A, Banta AB, Collins CC, Qi M, Trask BJ, Kuo WL, Cochran J, Costa T, Pierpont ME, Rand EB, Piccoli DA, Hood L, Spinner NB. Alagille syndrome is caused by mutations in human Jagged 1, which encodes a ligand for Notch 1. Nat Genet 1997: 16: 243-251.
-
(1997)
Nat Genet
, vol.16
, pp. 243-251
-
-
Li, L.1
Krantz, I.D.2
Deng, Y.3
Genin, A.4
Banta, A.B.5
Collins, C.C.6
Qi, M.7
Trask, B.J.8
Kuo, W.L.9
Cochran, J.10
Costa, T.11
Pierpont, M.E.12
Rand, E.B.13
Piccoli, D.A.14
Hood, L.15
Spinner, N.B.16
-
60
-
-
15144345481
-
-
http://www.ncbi.nlm.nih.gov/dbEST/index.html
-
-
-
-
61
-
-
15144353443
-
-
http://www3.ncbi.nlm.nih.gov/Omim/searchomim.html
-
-
-
-
62
-
-
15144361974
-
-
http://www.hgmp.mrc.ac.uk/DHMHD/lddb.html
-
-
-
-
63
-
-
15144351333
-
-
http://www.ncbi.nlm.nih.gov/UniGene/index.html
-
-
-
-
64
-
-
0030293334
-
Defining the boundaries of zebrafish developmental genetics
-
Felsenfeld AL. Defining the boundaries of zebrafish developmental genetics. Nat Genet 1996: 14: 258-263.
-
(1996)
Nat Genet
, vol.14
, pp. 258-263
-
-
Felsenfeld, A.L.1
-
65
-
-
0031901225
-
The Xenopus homologue of the Drosophila gene tailless has a function in early eye development
-
Hollemann T, Bellefroid E, Pieler T. The Xenopus homologue of the Drosophila gene tailless has a function in early eye development. Development 1998: 125: 2425-2432.
-
(1998)
Development
, vol.125
, pp. 2425-2432
-
-
Hollemann, T.1
Bellefroid, E.2
Pieler, T.3
-
66
-
-
15144355013
-
-
http://www.informatics.jax.org/
-
-
-
-
67
-
-
0029777408
-
Cyclopia and defective axial patterning in mice lacking Sonic Hedgehog gene function
-
Chiang C, Litingtung Y, Lee E, Yound KE, Corden JL, Westphal H, Beachy PA. Cyclopia and defective axial patterning in mice lacking Sonic Hedgehog gene function. Nature 1996: 383: 407-413.
-
(1996)
Nature
, vol.383
, pp. 407-413
-
-
Chiang, C.1
Litingtung, Y.2
Lee, E.3
Yound, K.E.4
Corden, J.L.5
Westphal, H.6
Beachy, P.A.7
-
68
-
-
0030294408
-
Mutations in the human Sonic Hedgehog gene cause holoprossencephaly
-
Roessler E, Belloni E, Gaudenz K, Jay P, Berta P, Scherer SW, Tsui LC, Muenke M. Mutations in the human Sonic Hedgehog gene cause holoprossencephaly. Nat Genet 1996: 14: 357-360.
-
(1996)
Nat Genet
, vol.14
, pp. 357-360
-
-
Roessler, E.1
Belloni, E.2
Gaudenz, K.3
Jay, P.4
Berta, P.5
Scherer, S.W.6
Tsui, L.C.7
Muenke, M.8
-
69
-
-
0028174023
-
Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret
-
Schuchardt A, D'Agati V, Larsson-Blomberg L, Costantini F, Pachnis V. Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret. Nature 1994: 367: 380-383.
-
(1994)
Nature
, vol.367
, pp. 380-383
-
-
Schuchardt, A.1
D'Agati, V.2
Larsson-Blomberg, L.3
Costantini, F.4
Pachnis, V.5
-
70
-
-
0028120882
-
Point mutations affecting the tyrosine kinase domain of the RET proto-oncogne in Hirschsprung's disease
-
Romeo G, Ronchetto P, Luo Y, Barone V, Sen M, Ceccherini I, Pasini B, bocciardi R, Lerone M, Kaariainen H. Point mutations affecting the tyrosine kinase domain of the RET proto-oncogne in Hirschsprung's disease. Nature 1994: 367: 377-378.
-
(1994)
Nature
, vol.367
, pp. 377-378
-
-
Romeo, G.1
Ronchetto, P.2
Luo, Y.3
Barone, V.4
Sen, M.5
Ceccherini, I.6
Pasini, B.7
Bocciardi, R.8
Lerone, M.9
Kaariainen, H.10
-
71
-
-
0031444287
-
The eye-specification proteins so and Eys form a complex and regulate multiple steps in Drosophila eye development
-
Pignoni F, Hu B, Zavitz KH, Xiao J, Garrity PA, Zipursky SL. The eye-specification proteins So and Eys form a complex and regulate multiple steps in Drosophila eye development. Cell 1997: 91: 881-891.
-
(1997)
Cell
, vol.91
, pp. 881-891
-
-
Pignoni, F.1
Hu, B.2
Zavitz, K.H.3
Xiao, J.4
Garrity, P.A.5
Zipursky, S.L.6
-
72
-
-
0031441007
-
The Drosophila eyes absent gene directs ectopic eye formation in pathway conserved between flies and vertebrates
-
Bonini NM, Bui QT, Gray-Board GL, Warrick JM. The Drosophila eyes absent gene directs ectopic eye formation in pathway conserved between flies and vertebrates. Development 1997: 124: 4819-4826.
-
(1997)
Development
, vol.124
, pp. 4819-4826
-
-
Bonini, N.M.1
Bui, Q.T.2
Gray-Board, G.L.3
Warrick, J.M.4
-
73
-
-
0028096639
-
Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing
-
Epstein JA, Glaser T, Cal J, Jepeal L, Walton DS, Maas RL. Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing. Genes Dev 1994: 8: 2022-2034.
-
(1994)
Genes Dev
, vol.8
, pp. 2022-2034
-
-
Epstein, J.A.1
Glaser, T.2
Cal, J.3
Jepeal, L.4
Walton, D.S.5
Maas, R.L.6
-
75
-
-
0030162151
-
PAX6 missense mutation in isolated foveal hypoplasia
-
Azuma N, Nishina S, Yanagisawa H, Okuyama T, Yamada M. PAX6 missense mutation in isolated foveal hypoplasia. Nat Genet 1996: 13: 141 142.
-
(1996)
Nat Genet
, vol.13
, pp. 141142
-
-
Azuma, N.1
Nishina, S.2
Yanagisawa, H.3
Okuyama, T.4
Yamada, M.5
-
76
-
-
0031984554
-
Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene
-
Alward WL, Semina EV, Kalenak JW, Heon E, Sheth BP, Stone EM, Murray JC. Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. Am J Opgthalmol 1998: 125: 98-100.
-
(1998)
Am J Opgthalmol
, vol.125
, pp. 98-100
-
-
Alward, W.L.1
Semina, E.V.2
Kalenak, J.W.3
Heon, E.4
Sheth, B.P.5
Stone, E.M.6
Murray, J.C.7
-
77
-
-
0031802075
-
Mutation in the RIEG1 gene in patient with iridogoniodysgenesis syndrome
-
Kulak SC, Kozlowski K, Semina EV, Pearce WG, Walter MA. Mutation in the RIEG1 gene in patient with iridogoniodysgenesis syndrome. Hum Mol Genet 1998: 7: 1113-1117.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1113-1117
-
-
Kulak, S.C.1
Kozlowski, K.2
Semina, E.V.3
Pearce, W.G.4
Walter, M.A.5
-
78
-
-
0031447030
-
Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration
-
Swain PK, Chen S, Wang QL, Affatigato LM, Coats CL, Brady KD, Fishman GA, Jacobson SG, Swaroop A, Stone E, Sieving PA, Zack DJ. Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration. Neuron 1997: 19: 1329-1336.
-
(1997)
Neuron
, vol.19
, pp. 1329-1336
-
-
Swain, P.K.1
Chen, S.2
Wang, Q.L.3
Affatigato, L.M.4
Coats, C.L.5
Brady, K.D.6
Fishman, G.A.7
Jacobson, S.G.8
Swaroop, A.9
Stone, E.10
Sieving, P.A.11
Zack, D.J.12
-
79
-
-
0030831115
-
The effect of peripherin/rds haploinsufficiency on rod and cone photoreceptors
-
Cheng T, Peachey NS, Li S, Goto Y, Cao Y, Naash MI. The effect of peripherin/rds haploinsufficiency on rod and cone photoreceptors. J Neurosci 1997: 17: 8118-8128.
-
(1997)
J Neurosci
, vol.17
, pp. 8118-8128
-
-
Cheng, T.1
Peachey, N.S.2
Li, S.3
Goto, Y.4
Cao, Y.5
Naash, M.I.6
-
80
-
-
0031255068
-
Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy
-
Gu SM, Thompson DA, Srikumari CR, Lorenz B, Finckh U, Micoletti A, Murthy KR, Rathmann M, Kumaramanickavel G, Denton MJ, Gal A. Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy. Nat Genet 1997: 17: 194-197.
-
(1997)
Nat Genet
, vol.17
, pp. 194-197
-
-
Gu, S.M.1
Thompson, D.A.2
Srikumari, C.R.3
Lorenz, B.4
Finckh, U.5
Micoletti, A.6
Murthy, K.R.7
Rathmann, M.8
Kumaramanickavel, G.9
Denton, M.J.10
Gal, A.11
-
82
-
-
0028952247
-
Homozygosity for Waardenburg syndrome
-
Zlotogora J, Lerer I, Bar-David S, Ergaz Z, Abeliovich D. Homozygosity for Waardenburg syndrome. Am J Hum Genet 1995: 56: 1173-1178.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1173-1178
-
-
Zlotogora, J.1
Lerer, I.2
Bar-David, S.3
Ergaz, Z.4
Abeliovich, D.5
-
83
-
-
0030914931
-
Pax6 is required for differentiation of glucagon-producing alpha-cells in mouse pancreas
-
St-Onge L, Sosa-Pineda B, Chowdhury K, Mansouri A, Gurss P. Pax6 is required for differentiation of glucagon-producing alpha-cells in mouse pancreas. Nature 1997: 387: 406-409.
-
(1997)
Nature
, vol.387
, pp. 406-409
-
-
St-Onge, L.1
Sosa-Pineda, B.2
Chowdhury, K.3
Mansouri, A.4
Gurss, P.5
-
84
-
-
13344249785
-
Ocular retardation mouse caused by Ch × 10 homeobox null allele: Impaired retinal progenitor proliferation and bipolar cell differentiation
-
Burmeister M, Novak J, Liang MY, Basu S, Ploder L, Hawes NL, Vidgen D, Hoover F, Goldman D, Kalnins VI, Roderick TH, Taylor BA, Hankin MH, McInnes RR. Ocular retardation mouse caused by Ch × 10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation. Nat Genet 1996: 12: 376-384.
-
(1996)
Nat Genet
, vol.12
, pp. 376-384
-
-
Burmeister, M.1
Novak, J.2
Liang, M.Y.3
Basu, S.4
Ploder, L.5
Hawes, N.L.6
Vidgen, D.7
Hoover, F.8
Goldman, D.9
Kalnins, V.I.10
Roderick, T.H.11
Taylor, B.A.12
Hankin, M.H.13
McInnes, R.R.14
-
85
-
-
0028091741
-
Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequence
-
Steingrimsson E, Moore KJ, Lamoreux ML, Ferre-D'Amare AR, Burley SK, Zimring DC, Skow LC, Hodgkinson CA, Arnheiter H, Copeland NG. Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequence. Nat Genet 1994: 8: 256-263.
-
(1994)
Nat Genet
, vol.8
, pp. 256-263
-
-
Steingrimsson, E.1
Moore, K.J.2
Lamoreux, M.L.3
Ferre-D'Amare, A.R.4
Burley, S.K.5
Zimring, D.C.6
Skow, L.C.7
Hodgkinson, C.A.8
Arnheiter, H.9
Copeland, N.G.10
-
86
-
-
0029188455
-
Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects
-
Ishibashi M, Ang SL, Shiota K, Nakanishi S, Kageyama R, Guillemot F. Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects. Genes Dev 1995: 9: 3136-3148.
-
(1995)
Genes Dev
, vol.9
, pp. 3136-3148
-
-
Ishibashi, M.1
Ang, S.L.2
Shiota, K.3
Nakanishi, S.4
Kageyama, R.5
Guillemot, F.6
-
87
-
-
0029977614
-
Mammalian hairy and Enhancer of split homolog 1 regulated differentiation of retinal neurons and is essential for eye morphogenesis
-
Tomita K, Ishibashi M, Nakahra K, Ang SL, Nakanishi S, Guillemot F, Kageyama R. Mammalian hairy and Enhancer of split homolog 1 regulated differentiation of retinal neurons and is essential for eye morphogenesis. Neuron 1996: 16: 723-734.
-
(1996)
Neuron
, vol.16
, pp. 723-734
-
-
Tomita, K.1
Ishibashi, M.2
Nakahra, K.3
Ang, S.L.4
Nakanishi, S.5
Guillemot, F.6
Kageyama, R.7
-
88
-
-
0030767662
-
Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development
-
Porter FD, Drago J, Xu Y, Cheema SS, Wassif C, Huang SP, Lee E, Grinberg A, Massalas JS, Bodine D, Alt F, Westphal H. Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development. Development 1997: 124: 2935-2944.
-
(1997)
Development
, vol.124
, pp. 2935-2944
-
-
Porter, F.D.1
Drago, J.2
Xu, Y.3
Cheema, S.S.4
Wassif, C.5
Huang, S.P.6
Lee, E.7
Grinberg, A.8
Massalas, J.S.9
Bodine, D.10
Alt, F.11
Westphal, H.12
-
89
-
-
0028895055
-
Mouse Otx2 functions in the formaiton and patterning of rostral head
-
Matsuo I, Kuratani S, Kimura C, Takeda N, Aizawa S. Mouse Otx2 functions in the formaiton and patterning of rostral head. Genes Dev 1995: 9: 2646-2658.
-
(1995)
Genes Dev
, vol.9
, pp. 2646-2658
-
-
Matsuo, I.1
Kuratani, S.2
Kimura, C.3
Takeda, N.4
Aizawa, S.5
-
90
-
-
15844384249
-
Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development
-
Erkman L, McEvilly RJ, Luo L, Ryan AK, Hooshmand F, O'Connell SM, Keithley EM, Rapaport DH, Ryan AF, Rosenfeld MG. Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development. Nature 1996: 381: 603-606.
-
(1996)
Nature
, vol.381
, pp. 603-606
-
-
Erkman, L.1
McEvilly, R.J.2
Luo, L.3
Ryan, A.K.4
Hooshmand, F.5
O'Connell, S.M.6
Keithley, E.M.7
Rapaport, D.H.8
Ryan, A.F.9
Rosenfeld, M.G.10
-
91
-
-
0031001710
-
The Rx homeobox gene is essential for vertebrate eye development
-
Mathers PH, Grinberg A, Mahon KA, Jamrich M. The Rx homeobox gene is essential for vertebrate eye development. Nature 1997: 387: 603-607.
-
(1997)
Nature
, vol.387
, pp. 603-607
-
-
Mathers, P.H.1
Grinberg, A.2
Mahon, K.A.3
Jamrich, M.4
-
92
-
-
0032521460
-
Sox1 directly regualtes the gamma-crystallin genes and is essential for lens development in mice
-
Nishiguchi S, Wood H, Kondoh H, Lovell-Badge R, Episkopou V. Sox1 directly regualtes the gamma-crystallin genes and is essential for lens development in mice. Genes Dev 1998: 12: 776-781.
-
(1998)
Genes Dev
, vol.12
, pp. 776-781
-
-
Nishiguchi, S.1
Wood, H.2
Kondoh, H.3
Lovell-Badge, R.4
Episkopou, V.5
-
93
-
-
0028832707
-
A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye
-
Dudley AT, Lyons KM, Robertson EJ. A requirement for bone morphogenetic protein-7 during development of the mammalian kidney and eye. Genes Dev 1995: 9: 2795-2807.
-
(1995)
Genes Dev
, vol.9
, pp. 2795-2807
-
-
Dudley, A.T.1
Lyons, K.M.2
Robertson, E.J.3
-
94
-
-
0028882261
-
BMP-7 is an inducer of nephrogenesis,and is also required for eye development and skeletal patterning
-
Luo G, Hofmann C, Bronckers AL, Sohocki M, Bradley A, Karsently G. BMP-7 is an inducer of nephrogenesis,and is also required for eye development and skeletal patterning. Genes Dev 1995: 9: 2808-2820.
-
(1995)
Genes Dev
, vol.9
, pp. 2808-2820
-
-
Luo, G.1
Hofmann, C.2
Bronckers, A.L.3
Sohocki, M.4
Bradley, A.5
Karsently, G.6
-
95
-
-
0031561724
-
BMP7 null mutation in mice: Developmental defects in skeleton, kidney, and eye
-
Jena N, Martin-Seisdedos C, McCue P, Croce CM. BMP7 null mutation in mice: developmental defects in skeleton, kidney, and eye. Exp Cell Res 1997: 230: 28-37.
-
(1997)
Exp Cell Res
, vol.230
, pp. 28-37
-
-
Jena, N.1
Martin-Seisdedos, C.2
McCue, P.3
Croce, C.M.4
-
96
-
-
0027730439
-
Genetic deletion of a neural cell adhesion molecule variant (N-CAM-180) produces distinct defects in the central nervous system
-
Tomasiewicz H, Ono K, Yee D, Thompson C, Goridis C, Rutishcuser U, Magnuson T. Genetic deletion of a neural cell adhesion molecule variant (N-CAM-180) produces distinct defects in the central nervous system. Neuron 1993: 11: 1163-1174.
-
(1993)
Neuron
, vol.11
, pp. 1163-1174
-
-
Tomasiewicz, H.1
Ono, K.2
Yee, D.3
Thompson, C.4
Goridis, C.5
Rutishcuser, U.6
Magnuson, T.7
|