-
1
-
-
0028807157
-
-1- mutants due to a defective anterior neuroectoderm specification during gastrulation
-
-1- mutants due to a defective anterior neuroectoderm specification during gastrulation. Development 121, 3279-3290.
-
(1995)
Development
, vol.121
, pp. 3279-3290
-
-
Acampora, D.1
Mazan, S.2
Lallemand, Y.3
Avantaggiato, V.4
Maury, M.5
Simeone, A.6
Brûlet, P.7
-
2
-
-
0030730823
-
Genetic control of brain morphogenesis through Otx gene dosage requirement
-
Acampora, D., Avantaggiato, V., Tuorto, F. and Simeone, A. (1997). Genetic control of brain morphogenesis through Otx gene dosage requirement. Development 124, 3639-3650.
-
(1997)
Development
, vol.124
, pp. 3639-3650
-
-
Acampora, D.1
Avantaggiato, V.2
Tuorto, F.3
Simeone, A.4
-
3
-
-
0032413733
-
Visceral endoderm-restricted translation of Otx1 mediates recovery of Otx2 requirements for specification of anterior neural plate and normal gastrulation
-
Acampora, D., Avantaggiato, V., Tuorto, F., Briata, P., Corte, G. and Simeone, A. (1998). Visceral endoderm-restricted translation of Otx1 mediates recovery of Otx2 requirements for specification of anterior neural plate and normal gastrulation. Development 125, 5091-5104.
-
(1998)
Development
, vol.125
, pp. 5091-5104
-
-
Acampora, D.1
Avantaggiato, V.2
Tuorto, F.3
Briata, P.4
Corte, G.5
Simeone, A.6
-
4
-
-
0027992820
-
Positive and negative signals from mesoderm regulate the expression of mouse Otx2 in ectoderm explants
-
Ang, S. L., Conlon, R. A., Jin, O. and Rossant, J. (1994). Positive and negative signals from mesoderm regulate the expression of mouse Otx2 in ectoderm explants. Development 120, 2979-2989.
-
(1994)
Development
, vol.120
, pp. 2979-2989
-
-
Ang, S.L.1
Conlon, R.A.2
Jin, O.3
Rossant, J.4
-
5
-
-
0030050751
-
A targeted mouse Otx2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain
-
Ang, S.-L., Jin, O., Rhinn, M., Daigle, N., Stevenson, L. and Rossant, J. (1996). A targeted mouse Otx2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain. Development 122, 243-252.
-
(1996)
Development
, vol.122
, pp. 243-252
-
-
Ang, S.-L.1
Jin, O.2
Rhinn, M.3
Daigle, N.4
Stevenson, L.5
Rossant, J.6
-
6
-
-
0003764871
-
QTL Cartographer: A reference manual and tutorial for QTL mapping
-
Program in Statistical Genetics, Department of Statistics, North Carolina State University
-
Basten, C. J., Weir, B. S. and Zeng, Z.-B. (2001). QTL Cartographer: A reference manual and tutorial for QTL mapping. Program in Statistical Genetics, Department of Statistics, North Carolina State University.
-
(2001)
-
-
Basten, C.J.1
Weir, B.S.2
Zeng, Z.-B.3
-
7
-
-
0031767841
-
Prx1 and Prx2 in skeletogenesis: Roles in the craniofacial region, inner ear and limbs
-
Berge, D. t., Brouwer, A., Korving, J., Martin, J. F. and Meijlink, F. (1998a). Prx1 and Prx2 in skeletogenesis: roles in the craniofacial region, inner ear and limbs. Development 125, 3831-3842.
-
(1998)
Development
, vol.125
, pp. 3831-3842
-
-
Berge, D.T.1
Brouwer, A.2
Korving, J.3
Martin, J.F.4
Meijlink, F.5
-
8
-
-
0032105472
-
Mouse Alx3: An aristaless-like homeobox gene expressed during embryogenesis in ectomesenchyme and lateral plate mesoderm
-
Berge, D. t., Brouwer, A., Bahi, S. E., Guenet, J.-L., Robert, B. and Meijlink, F. (1998b). Mouse Alx3: An aristaless-like homeobox gene expressed during embryogenesis in ectomesenchyme and lateral plate mesoderm. Dev. Biol. 199, 11-25.
-
(1998)
Dev. Biol
, vol.199
, pp. 11-25
-
-
Berge, D.T.1
Brouwer, A.2
Bahi, S.E.3
Guenet, J.-L.4
Robert, B.5
Meijlink, F.6
-
9
-
-
0021776346
-
Agnathia-holoprosencephaly: A developmental field complex involving face and brain. Report of 3 cases
-
Bixler, D., Ward, R. and Gale, D. D. (1985). Agnathia-holoprosencephaly: a developmental field complex involving face and brain. Report of 3 cases. J. Craniofac. Genet. Dev. Biol. Suppl. 1, 241-249.
-
(1985)
J. Craniofac. Genet. Dev. Biol. Suppl
, vol.1
, pp. 241-249
-
-
Bixler, D.1
Ward, R.2
Gale, D.D.3
-
10
-
-
0031694448
-
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired
-
Brown, S. A., Warburton, D., Brown, L. Y., Yu, C. Y., Roeder, E. R., Stengel-Rutkowski, S., Hennekam, R. C. and Muenke, M. (1998). Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired. Nat. Genet. 20, 180-183.
-
(1998)
Nat. Genet
, vol.20
, pp. 180-183
-
-
Brown, S.A.1
Warburton, D.2
Brown, L.Y.3
Yu, C.Y.4
Roeder, E.R.5
Stengel-Rutkowski, S.6
Hennekam, R.C.7
Muenke, M.8
-
11
-
-
0032544679
-
Human CART1, a paired-class homeodomain protein, activates transcription through palindromic binding sites
-
Cai, R. L. (1998). Human CART1, a paired-class homeodomain protein, activates transcription through palindromic binding sites. Biochem. Bioph. Res. Comm. 250, 305-311.
-
(1998)
Biochem. Bioph. Res. Comm
, vol.250
, pp. 305-311
-
-
Cai, R.L.1
-
12
-
-
0027415509
-
The triple origin of skull in higher vertebrates: A study in quail-chick chimeras
-
Couly, G. F., Colley, P. M. and le Douarin, N. M. (1993). The triple origin of skull in higher vertebrates: a study in quail-chick chimeras. Development 117, 409-429.
-
(1993)
Development
, vol.117
, pp. 409-429
-
-
Couly, G.F.1
Colley, P.M.2
le Douarin, N.M.3
-
13
-
-
0026471778
-
MHox: A mesodermally restricted homeodomain protein that binds an essential site in the muscle creatine kinase enhancer
-
Cserjesi, P., Lilly, B., Bryson, L., Wang, Y., Sassoon, D. A. and Olson, E. N. (1992). MHox: a mesodermally restricted homeodomain protein that binds an essential site in the muscle creatine kinase enhancer. Development 115, 1087-1101.
-
(1992)
Development
, vol.115
, pp. 1087-1101
-
-
Cserjesi, P.1
Lilly, B.2
Bryson, L.3
Wang, Y.4
Sassoon D.A. Olson, E.N.5
-
14
-
-
0031975307
-
Experimental strategies for the genetic dissection of complex traits in animal models
-
Darvasi, A. (1998). Experimental strategies for the genetic dissection of complex traits in animal models. Nat. Genet. 18, 19-24.
-
(1998)
Nat. Genet
, vol.18
, pp. 19-24
-
-
Darvasi, A.1
-
15
-
-
17344362762
-
Mutations in the homeobox gene HESX1/Hesxl associated with septo-optic dysplasia in human and mouse
-
Dattani, M. T., Martinez-Barbera, J. P., Thomas, P. Q., Brickman, J. M., Gupta, R., Martensson, I.-L., Toresson, H., Fox, M., Wales, J. K. H., Hindmarsh, P. C. et al. (1998). Mutations in the homeobox gene HESX1/Hesxl associated with septo-optic dysplasia in human and mouse. Nat. Genet. 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
Martensson, I.-L.6
Toresson, H.7
Fox, M.8
Wales, J.K.H.9
Hindmarsh, P.C.10
-
16
-
-
0026645062
-
A genetic map of the mouse suitable for typing intraspecific crosses
-
Dietrich, W., Katz, H., Lincoln, S. E., Shin, H.-S., Friedman, J., Dracopoli, N. C. and Lander, E. S. (1992). A genetic map of the mouse suitable for typing intraspecific crosses. Genetics 131, 423-447.
-
(1992)
Genetics
, vol.131
, pp. 423-447
-
-
Dietrich, W.1
Katz, H.2
Lincoln, S.E.3
Shin, H.-S.4
Friedman, J.5
Dracopoli, N.C.6
Lander, E.S.7
-
17
-
-
0028302127
-
A genetic map of the mouse with 4,006 simple sequence length polymorphisms
-
Dietrich, W. F., Miller., J. C., Steen, R. G., Merchant, M., Damron, D., NAhf, R., Gross, A., Joyce, D. C., Wessel, M., Dredge, R. D. et al. (1994). A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nat. Genet. 7, 220-245.
-
(1994)
Nat. Genet
, vol.7
, pp. 220-245
-
-
Dietrich, W.F.1
Miller, J.C.2
Steen, R.G.3
Merchant, M.4
Damron, D.5
NAhf, R.6
Gross, A.7
Joyce, D.C.8
Wessel, M.9
Dredge, R.D.10
-
18
-
-
0010753072
-
Reconstruction of brain and ventricle system in an anchyote prosophthalmic otocephalic newborn cephalothoracopagus rabbit
-
Faller, A. and Rossier, B. (1969). Reconstruction of brain and ventricle system in an anchyote prosophthalmic otocephalic newborn cephalothoracopagus rabbit. Acta Anat. 73, 2-31.
-
(1969)
Acta Anat
, vol.73
, pp. 2-31
-
-
Faller, A.1
Rossier, B.2
-
19
-
-
0001173773
-
Genetics and manifold effects of Strong's luxoid gene in the mouse, including its interactions with Green's luxoid and Carter's luxate genes
-
Forsthoetel, P. F. (1962). Genetics and manifold effects of Strong's luxoid gene in the mouse, including its interactions with Green's luxoid and Carter's luxate genes. J. Morphol. 110, 391-420.
-
(1962)
J. Morphol
, vol.110
, pp. 391-420
-
-
Forsthoetel, P.F.1
-
20
-
-
0014314898
-
Responses to selection for plus and minus modifiers of some effects of Strong's luxoid gene on the mouse skeleton
-
Forsthoefel, P. F. (1968). Responses to selection for plus and minus modifiers of some effects of Strong's luxoid gene on the mouse skeleton. Teratology 1, 339-51.
-
(1968)
Teratology
, vol.1
, pp. 339-351
-
-
Forsthoefel, P.F.1
-
21
-
-
16744368142
-
Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination
-
Gripp, K. W., Wotton, D., Edwards, M. C., Roessler, E., Ades, L., Meinecke, P., Richieri-Costa, A., Zackai, E. H., Massague, J., Muenke, M. and Elledge, S. J. (2000). Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination. Nat. Genet. 25, 205-208.
-
(2000)
Nat. Genet
, vol.25
, pp. 205-208
-
-
Gripp, K.W.1
Wotton, D.2
Edwards, M.C.3
Roessler, E.4
Ades, L.5
Meinecke, P.6
Richieri-Costa, A.7
Zackai, E.H.8
Massague, J.9
Muenke, M.10
Elledge, S.J.11
-
22
-
-
0029045063
-
Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton: Evidence for unique and redundant function
-
Horan, G. S. B., Kovacs, E. N., Behringer, R. R. and Featherstone, M. S. (1995). Mutations in paralogous Hox genes result in overlapping homeotic transformations of the axial skeleton: evidence for unique and redundant function. Dev. Biol. 169, 359-372.
-
(1995)
Dev. Biol
, vol.169
, pp. 359-372
-
-
Horan, G.S.B.1
Kovacs, E.N.2
Behringer, R.R.3
Featherstone, M.S.4
-
23
-
-
0030008591
-
Contribution of early-emigrating midbrain crest cells to the dental mesenchyme of mandibular molar teeth in rat embryos
-
Imai, H., Osumi-Yamashita, N., Ninomiya, Y. and Eto, K. (1996). Contribution of early-emigrating midbrain crest cells to the dental mesenchyme of mandibular molar teeth in rat embryos. Dev. Biol. 176, 151-165.
-
(1996)
Dev. Biol
, vol.176
, pp. 151-165
-
-
Imai, H.1
Osumi-Yamashita, N.2
Ninomiya, Y.3
Eto, K.4
-
24
-
-
0029022716
-
Multiple trait analysis of genetic mapping for quantitative trait loci
-
Jiang, C. and Zeng, Z.-B. (1995) Multiple trait analysis of genetic mapping for quantitative trait loci. Genetics 140, 1111-1127.
-
(1995)
Genetics
, vol.140
, pp. 1111-1127
-
-
Jiang, C.1
Zeng, Z.-B.2
-
25
-
-
0022258053
-
Genetic and developmental studies of a new mouse mutation that produces otocephaly
-
Juriloff, D. M., Sulik, K. K., Roderick, T. H. and Hogan, B. K. (1985). Genetic and developmental studies of a new mouse mutation that produces otocephaly. J. Craniofac. Genet. Dev. Biol. 5, 121-145.
-
(1985)
J. Craniofac. Genet. Dev. Biol
, vol.5
, pp. 121-145
-
-
Juriloff, D.M.1
Sulik, K.K.2
Roderick, T.H.3
Hogan, B.K.4
-
26
-
-
84907133584
-
A modified differential stain for cartilage and bone in whole mount preparations of mammalian fetuses and small vertebrates
-
Kelly, W. L. and Bryden, M. M. (1983). A modified differential stain for cartilage and bone in whole mount preparations of mammalian fetuses and small vertebrates. Stain Technol. 58, 131-134.
-
(1983)
Stain Technol
, vol.58
, pp. 131-134
-
-
Kelly, W.L.1
Bryden, M.M.2
-
27
-
-
0030774258
-
Cis-acting elements conserved between mouse and pufferfish Otx2 genes govern the expression in mesencephalic neural crest cells
-
Kimura, C., Takeda, N., Suzuki, M., Oshimura, M., Aizawa, S. and Matson, I. (1997). Cis-acting elements conserved between mouse and pufferfish Otx2 genes govern the expression in mesencephalic neural crest cells. Development 124, 3929-3941.
-
(1997)
Development
, vol.124
, pp. 3929-3941
-
-
Kimura, C.1
Takeda, N.2
Suzuki, M.3
Oshimura, M.4
Aizawa, S.5
Matson, I.6
-
28
-
-
0034665631
-
Visceral endoderm mediates forebrain development by suppressing posteriorizing signals
-
Kimura, C., Yoshinaga, K., Tian, E., Suzuki, M., Aizawa, S. and Matsuo, I. (2000). Visceral endoderm mediates forebrain development by suppressing posteriorizing signals. Dev. Biol. 225, 304-321.
-
(2000)
Dev. Biol
, vol.225
, pp. 304-321
-
-
Kimura, C.1
Yoshinaga, K.2
Tian, E.3
Suzuki, M.4
Aizawa, S.5
Matsuo, I.6
-
29
-
-
0034957797
-
Complementary functions of Otx2 and Cripto in initial patterning of mouse epiblast
-
Kimura, C., Shen, M. M., Takeda, N., Aizawa, S. and Matsuo, I. (2001). Complementary functions of Otx2 and Cripto in initial patterning of mouse epiblast. Dev. Biol. 235, 12-32.
-
(2001)
Dev. Biol
, vol.235
, pp. 12-32
-
-
Kimura, C.1
Shen, M.M.2
Takeda, N.3
Aizawa, S.4
Matsuo, I.5
-
30
-
-
0029828103
-
Rhombencephalic neural crest segmentation is preserved throughout craniofacial ontogeny
-
Koentges, G. and Lumsden, A. (1996). Rhombencephalic neural crest segmentation is preserved throughout craniofacial ontogeny. Development 122, 3229-3242.
-
(1996)
Development
, vol.122
, pp. 3229-3242
-
-
Koentges, G.1
Lumsden, A.2
-
31
-
-
0024508964
-
Mapping mendelian factors underlying quantitative traits using RFLP linkage maps
-
Lander, E. S. and Botstein, D. (1989). Mapping mendelian factors underlying quantitative traits using RFLP linkage maps. Genetics 121, 185-199.
-
(1989)
Genetics
, vol.121
, pp. 185-199
-
-
Lander, E.S.1
Botstein, D.2
-
32
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander, E. S. and Schork, N. J. (1994). Genetic dissection of complex traits. Science 265, 2037-2048.
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
33
-
-
0028877463
-
Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
-
Lander, E. and Kruglyak, L. (1995). Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat. Genet. 11, 241-247.
-
(1995)
Nat. Genet
, vol.11
, pp. 241-247
-
-
Lander, E.1
Kruglyak, L.2
-
34
-
-
0032433267
-
Strain-dependent embryonic lethality in mice lacking the retinoblastoma-related p130 gene
-
LeCouter, J. E., Kablar, B., Whyte, P. F. M., Ying, C. and Rudnicki, M. A. (1998). Strain-dependent embryonic lethality in mice lacking the retinoblastoma-related p130 gene. Development 125, 4669-4679.
-
(1998)
Development
, vol.125
, pp. 4669-4679
-
-
LeCouter, J.E.1
Kablar, B.2
Whyte, P.F.M.3
Ying, C.4
Rudnicki, M.A.5
-
36
-
-
0029162584
-
Dorsaldifferentiation of neural plate cells induced by BMP-mediated signals from epidermal ectoderm
-
Liem, K. F., Jr, Tremml, G., Roelink, H. and Jessell, T. M. (1995). Dorsal differentiation of neural plate cells induced by BMP-mediated signals from epidermal ectoderm. Cell 82, 969-979.
-
(1995)
Cell
, vol.82
, pp. 969-979
-
-
Liem K.F., Jr.1
Tremml, G.2
Roelink, H.3
Jessell, T.M.4
-
37
-
-
0025354122
-
Towards construction of a high resolution map of the mouse genome using PCR-analyzed microsatellites
-
Love, J. M., Knight, A. M., McAleer, M. A. and Todd, J. A. (1990). Towards construction of a high resolution map of the mouse genome using PCR-analyzed microsatellites. Nucleic Acids Res. 18, 4123-4130.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 4123-4130
-
-
Love, J.M.1
Knight, A.M.2
McAleer, M.A.3
Todd, J.A.4
-
38
-
-
0033000566
-
prx-1 functions cooperatively with another paired-related homeobox gene, prx-2, to maintain cell fates within the craniofacial mesenchyme
-
Lu, M.-F., Cheng, H.-T., Kern, M. J., Potter, S. S., Tran, B., Diekwisch, T. G. H. and Martin, J. F. (1999). prx-1 functions cooperatively with another paired-related homeobox gene, prx-2, to maintain cell fates within the craniofacial mesenchyme. Development 126, 495-504.
-
(1999)
Development
, vol.126
, pp. 495-504
-
-
Lu, M.-F.1
Cheng, H.-T.2
Kern, M.J.3
Potter, S.S.4
Tran, B.5
Diekwisch, T.G.H.6
Martin, J.F.7
-
39
-
-
0017741766
-
Holoprosencephaly in human embryos: Epidemiologic studies of 150 cases
-
Matsunaga, E. and Shiota, K. (1977). Holoprosencephaly in human embryos: Epidemiologic studies of 150 cases. Teratology 16, 261-272.
-
(1977)
Teratology
, vol.16
, pp. 261-272
-
-
Matsunaga, E.1
Shiota, K.2
-
40
-
-
0028895055
-
Mouse Otx2 functions in the formation and patterning of rostral head
-
Matsuo, I, Kuratani, S., Kimura, C., Takeda, N. and Aizawa, S. (1995). Mouse Otx2 functions in the formation and patterning of rostral head. Genes Dev. 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
-
41
-
-
0035158663
-
Haploinsufficiency of the human homeobox gene ALK4 causes skull ossification defects
-
Mavrogiannis, L. A., Antonopoulou, L, Baxova, A., Kutilek, S., Kim, C. A., Sugayama, S. M., Salamanca, A., Wall, S. A., Morris-Kay, G. M. and Wilkie, A. O. M. (2001). Haploinsufficiency of the human homeobox gene ALK4 causes skull ossification defects. Nat. Genet 27, 17-18.
-
(2001)
Nat. Genet
, vol.27
, pp. 17-18
-
-
Mavrogiannis, L.A.1
Antonopoulou, L.2
Baxova, A.3
Kutilek, S.4
Kim, C.A.5
Sugayama, S.M.6
Salamanca, A.7
Wall, S.A.8
Morris-Kay, G.M.9
Wilkie, A.O.M.10
-
42
-
-
0032732443
-
The mutational spectrum of the Sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly
-
Nanni, L., Ming, J. E., Bocian, M., Steinhaus, K., Bianchi, D. W., Die-Smulders, C., Giannotti, A., Imaizumi, K., Jones, K. L., Campo, M. D. et al. (1999). The mutational spectrum of the Sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly. Hum. Mol. Genet. 8, 2479-2488.
-
(1999)
Hum. Mol. Genet
, vol.8
, pp. 2479-2488
-
-
Nanni, L.1
Ming, J.E.2
Bocian, M.3
Steinhaus, K.4
Bianchi, D.W.5
Die-Smulders, C.6
Giannotti, A.7
Imaizumi, K.8
Jones, K.L.9
Campo, M.D.10
-
43
-
-
0010745283
-
Letter to the editors
-
Opitz, J. M. (1980). Letter to the editors. Clin. Genet. 17, 69-71.
-
(1980)
Clin. Genet
, vol.17
, pp. 69-71
-
-
Opitz, J.M.1
-
44
-
-
0028147035
-
The contribution of both forebrain and midbrain crest cells to the mesenchyme in the frontonasal mass of mouse embryos
-
Osumi-Yamashita, N., Ninomiya, Y., Doi, H. and Eto, K. (1994). The contribution of both forebrain and midbrain crest cells to the mesenchyme in the frontonasal mass of mouse embryos. Dev. Biol. 164, 409-419.
-
(1994)
Dev. Biol
, vol.164
, pp. 409-419
-
-
Osumi-Yamashita, N.1
Ninomiya, Y.2
Doi, H.3
Eto, K.4
-
45
-
-
0020641310
-
Familial agnathia-holoprosencephaly
-
Pauli, R. M., Pettersen, J. C., Arya, S. and Gilbert, E. F. (1983). Familial agnathia-holoprosencephaly. Am. J. Med. Genet. 14, 677-698.
-
(1983)
Am. J. Med. Genet
, vol.14
, pp. 677-698
-
-
Pauli, R.M.1
Pettersen, J.C.2
Arya, S.3
Gilbert, E.F.4
-
46
-
-
0028972869
-
Transforming growth factor-β3 is required for secondary palate fusion
-
Proetzel, G., Pawlowski, S. A., Wiles, M. V., Yin, M., Boivin, G. P., Howles, P. N., Ding, J., Ferguson, M. W. J. and Doetschman, T. (1995). Transforming growth factor-β3 is required for secondary palate fusion. Nat. Genet. 11, 409-414.
-
(1995)
Nat. Genet
, vol.11
, pp. 409-414
-
-
Proetzel, G.1
Pawlowski, S.A.2
Wiles, M.V.3
Yin, M.4
Boivin, G.P.5
Howles, P.N.6
Ding, J.7
Ferguson, M.W.J.8
Doetschman, T.9
-
47
-
-
0030608661
-
Alx4:cDNA cloning and characterization of a novel paired-type homeodomain protein
-
Qu, S., Li, L. and Wisdom, R. (1997). Alx4:cDNA cloning and characterization of a novel paired-type homeodomain protein. Gene 203, 217-223.
-
(1997)
Gene
, vol.203
, pp. 217-223
-
-
Qu, S.1
Li, L.2
Wisdom, R.3
-
48
-
-
0031875540
-
Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly
-
Qu, S., Tucker, S. C., Ehrlich, J. S., Levorse, J. M., Flaherty, L. A., Wisdom, R. and Vogt, T. F. (1998). Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly. Development 125, 2711-2721.
-
(1998)
Development
, vol.125
, pp. 2711-2721
-
-
Qu, S.1
Tucker, S.C.2
Ehrlich, J.S.3
Levorse, J.M.4
Flaherty, L.A.5
Wisdom, R.6
Vogt, T.F.7
-
49
-
-
0032915190
-
Physical and genetic interactions between Alx4 and Cart1
-
Qu, S., Tucker, S. C., Zhao, Q., deCrombrugghe, B. and Wisdom, R. (1999). Physical and genetic interactions between Alx4 and Cart1. Development 126, 359-369.
-
(1999)
Development
, vol.126
, pp. 359-369
-
-
Qu, S.1
Tucker, S.C.2
Zhao, Q.3
deCrombrugghe, B.4
Wisdom, R.5
-
50
-
-
0030294408
-
Mutations in the human Sonic Hedgehog gene cause holoprosencephaly
-
Roessler, E., Belloni, E., Gaudenz, K., Jay, P., Berta, P., Scherer, S. W., Tsui, L. C. and Muenke, M. (1996). Mutations in the human Sonic Hedgehog gene cause holoprosencephaly. Nat. Genet. 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
-
51
-
-
13344282728
-
Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor
-
Rozmahel, R., Wilschanski, M., Matin, A., Plyte, S., Oliver, M., Auerbach, W., Moore, A., Forstner, J., Durie, P., Nadeau, J., Bear, C. and Tsui, L.-C. (1996). Modulation of disease severity in cystic fibrosis transmembrane conductance regulator deficient mice by a secondary genetic factor. Nat. Genet. 12, 280-287.
-
(1996)
Nat. Genet
, vol.12
, pp. 280-287
-
-
Rozmahel, R.1
Wilschanski, M.2
Matin, A.3
Plyte, S.4
Oliver, M.5
Auerbach, W.6
Moore, A.7
Forstner, J.8
Durie, P.9
Nadeau, J.10
Bear, C.11
Tsui, L.-C.12
-
52
-
-
0004136246
-
-
2nd edn. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press
-
Sambrook, J., Fritsch, E. F. and Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
-
(1989)
Molecular Cloning: A Laboratory Manual
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
53
-
-
0028928779
-
Origins of the avian neural crest: The role of neural plate-epidermal interactions
-
Selleck, M. A. and Bronner-Fraser, M. (1995). Origins of the avian neural crest: the role of neural plate-epidermal interactions. Development 121, 525-538.
-
(1995)
Development
, vol.121
, pp. 525-538
-
-
Selleck, M.A.1
Bronner-Fraser, M.2
-
54
-
-
0026759308
-
Nested expression domains of four homeobox genes in developing rostral brain
-
Simeone, A., Acampora, D., Gulisano, M., Stornaiuolo, A. and Boncinelli, E. (1992). Nested expression domains of four homeobox genes in developing rostral brain. Nature 358, 687-690.
-
(1992)
Nature
, vol.358
, pp. 687-690
-
-
Simeone, A.1
Acampora, D.2
Gulisano, M.3
Stornaiuolo, A.4
Boncinelli, E.5
-
55
-
-
0027260743
-
A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo
-
Simeone, A., Acampora, D., Mallamaci, A., Stornaiuolo, A., D'Apice, M. R., Nigro, V. and Boncinelli, E. (1993). A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo. EMBO J. 12, 2735-2747.
-
(1993)
EMBO J
, vol.12
, pp. 2735-2747
-
-
Simeone, A.1
Acampora, D.2
Mallamaci, A.3
Stornaiuolo, A.4
D'Apice, M.R.5
Nigro, V.6
Boncinelli, E.7
-
56
-
-
0014352261
-
Agnathia and micrognathia in the sheep
-
Smith, I. D. (1968). Agnathia and micrognathia in the sheep. Aust. Vet. J. 44, 510-511.
-
(1968)
Aust. Vet. J
, vol.44
, pp. 510-511
-
-
Smith, I.D.1
-
57
-
-
0030280509
-
Otx1 function overlaps with Otx2 in development of mouse forebrain and midbrain
-
Suda, Y., Matsuo, I., Kuratani, S. and Aizawa, S. (1996). Otx1 function overlaps with Otx2 in development of mouse forebrain and midbrain. Genes Cells 1, 1031-1044.
-
(1996)
Genes Cells
, vol.1
, pp. 1031-1044
-
-
Suda, Y.1
Matsuo, I.2
Kuratani, S.3
Aizawa, S.4
-
58
-
-
0031282965
-
Cooperation between Otx1 and Otx2 genes in developmental patterning of rostral brain
-
Suda, Y., Matsuo, I. and Aizawa, S. (1997). Cooperation between Otx1 and Otx2 genes in developmental patterning of rostral brain. Mech. Dev. 69, 125-141.
-
(1997)
Mech. Dev
, vol.69
, pp. 125-141
-
-
Suda, Y.1
Matsuo, I.2
Aizawa, S.3
-
59
-
-
0034915990
-
Emx2 directs the development of diencephalon in cooperation with Otx2
-
Suda, Y., Hossain, Z. M., Kobayashi, C., Hatano, O., Yoshida, M., Matsuo, I. and Aizawa, S. (2001). Emx2 directs the development of diencephalon in cooperation with Otx2. Development 128, 2433-2450.
-
(2001)
Development
, vol.128
, pp. 2433-2450
-
-
Suda, Y.1
Hossain, Z.M.2
Kobayashi, C.3
Hatano, O.4
Yoshida, M.5
Matsuo, I.6
Aizawa, S.7
-
60
-
-
0037083389
-
Otx2 is required to respond to signals from anterior neural ridge for forebrain specification
-
Tian, E, Kimura, C., Takeda, N., Aizawa, S. and Matsuo, I. (2002). Otx2 is required to respond to signals from anterior neural ridge for forebrain specification. Dev. Biol. 242, 204-223.
-
(2002)
Dev. Biol
, vol.242
, pp. 204-223
-
-
Tian, E.1
Kimura, C.2
Takeda, N.3
Aizawa, S.4
Matsuo, I.5
-
61
-
-
0032759342
-
Molecular mechanisms of holoprosencephaly
-
Wallis, D. E. and Muenke, M. (1999). Molecular mechanisms of holoprosencephaly. Mol. Genet. Metab. 68, 126-138.
-
(1999)
Mol. Genet. Metab
, vol.68
, pp. 126-138
-
-
Wallis, D.E.1
Muenke, M.2
-
62
-
-
0033855246
-
Mutations in holoprosencephaly
-
Wallis, D. E. and Muenke, M. (2000). Mutations in holoprosencephaly. Hum. Mutat. 16, 99-108.
-
(2000)
Hum. Mutat
, vol.16
, pp. 99-108
-
-
Wallis, D.E.1
Muenke, M.2
-
63
-
-
0033064156
-
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly
-
Wallis, D. E., Roessler, E., Hehr, U., Nanni, L., Wiltshire, T., Richieri-Costa, A., Gillessen-Kaesbach, G., Zackai, E. H., Rommens, J. and Muenke, M. (1999). Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly. Nat. Genet. 22, 196-198.
-
(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
-
64
-
-
0033105981
-
BMP7 acts in murine lens placode development
-
Wawersik, S., Purcell, P., Rauchman, M., Dudley, A. T., Robertson, E. J. and Maas, R. (1999). BMP7 acts in murine lens placode development. Dev. Biol. 207, 176-188.
-
(1999)
Dev. Biol
, vol.207
, pp. 176-188
-
-
Wawersik, S.1
Purcell, P.2
Rauchman, M.3
Dudley, A.T.4
Robertson, E.J.5
Maas, R.6
-
65
-
-
0013871247
-
Congenital otocephalus in a lamb
-
Willson, J. E. (1966). Congenital otocephalus in a lamb. Vet. Med. Small Anim. Clin. 61, 58-59.
-
(1966)
Vet. Med. Small Anim. Clin
, vol.61
, pp. 58-59
-
-
Willson, J.E.1
-
66
-
-
0030031950
-
What's in a face?
-
Winter, R. M. (1996). What's in a face? Nat. Genet. 12, 124-129.
-
(1996)
Nat. Genet
, vol.12
, pp. 124-129
-
-
Winter, R.M.1
-
67
-
-
0032143608
-
Craf-1 protein kinase is essential for mouse development
-
Wojnowski, L., Stancato, L. F., Zimmer, A. M., Hahn, H., Beck, T. W., Larner, A. C., Rapp, U. R. and Zimmer, A. (1998). Craf-1 protein kinase is essential for mouse development. Mech. Dev. 76, 141-149.
-
(1998)
Mech. Dev
, vol.76
, pp. 141-149
-
-
Wojnowski, L.1
Stancato, L.F.2
Zimmer, A.M.3
Hahn, H.4
Beck, T.W.5
Larner, A.C.6
Rapp, U.R.7
Zimmer, A.8
-
68
-
-
85027471398
-
Types of subnormal development of the head from inbred strains of guinea pigs and their bearing on the classification and interpretation of vertebrate monsters
-
Wright, S. and Wagner, K. (1934). Types of subnormal development of the head from inbred strains of guinea pigs and their bearing on the classification and interpretation of vertebrate monsters. Am. J. Anat. 54, 383-447.
-
(1934)
Am. J. Anat
, vol.54
, pp. 383-447
-
-
Wright, S.1
Wagner, K.2
-
69
-
-
0033759656
-
Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome
-
Wu, Y. Q., Badano, J. L., McCaskill, C., Vogel, H., Potocki, L. and Shaffer, L. G. (2000). Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome. Am. J. Hum. Genet. 67, 1327-1332.
-
(2000)
Am. J. Hum. Genet
, vol.67
, pp. 1327-1332
-
-
Wu, Y.Q.1
Badano, J.L.2
McCaskill, C.3
Vogel, H.4
Potocki, L.5
Shaffer, L.G.6
-
70
-
-
0034530307
-
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)
-
Wuyts, W., Cleiren, E., Homfray, T., Rasore-Quartino, A., Vanhoenacker, F. and van Hul, W. (2000). The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500). J. Med Genet. 37, 916-920.
-
(2000)
J. Med Genet
, vol.37
, pp. 916-920
-
-
Wuyts, W.1
Cleiren, E.2
Homfray, T.3
Rasore-Quartino, A.4
Vanhoenacker, F.5
van Hul, W.6
-
71
-
-
0027440811
-
A novel ES cell line, TT2, with high germline-differentiating potency
-
Yagi, T., Tokunaga, T., Furuta, Y., Nada, S., Yoshida, M., Tsukada, T., Saga, Y., Takeda, N., Ikawa, Y. and Aizawa, S. (1993). A novel ES cell line, TT2, with high germline-differentiating potency. Anal. Biochem. 214, 70-76.
-
(1993)
Anal. Biochem
, vol.214
, pp. 70-76
-
-
Yagi, T.1
Tokunaga, T.2
Furuta, Y.3
Nada, S.4
Yoshida, M.5
Tsukada, T.6
Saga, Y.7
Takeda, N.8
Ikawa, Y.9
Aizawa, S.10
-
72
-
-
0028224156
-
Precision mapping of quantitative trait loci
-
Zeng, Z.-B. (1994). Precision mapping of quantitative trait loci. Genetics 136, 1457-1468.
-
(1994)
Genetics
, vol.136
, pp. 1457-1468
-
-
Zeng, Z.-B.1
-
73
-
-
0027973640
-
The gene for homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development
-
Zhao, G.-Q., Eberspaecher, H., Seldin, M. F. and de Crombrugghe, B. (1994). The gene for homeodomain-containing protein Cart-1 is expressed in cells that have a chondrogenic potential during embryonic development. Mech. Dev. 48, 245-254.
-
(1994)
Mech. Dev
, vol.48
, pp. 245-254
-
-
Zhao, G.-Q.1
Eberspaecher, H.2
Seldin, M.F.3
de Crombrugghe, B.4
-
74
-
-
0029946542
-
Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene
-
Zhao, Q., Behringer, R. R. and de Crombrugghe, B. (1996). Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene. Nat. Genet. 13, 275-283.
-
(1996)
Nat. Genet
, vol.13
, pp. 275-283
-
-
Zhao, Q.1
Behringer, R.R.2
de Crombrugghe, B.3
-
75
-
-
0033405143
-
Oto is a homeotic locus with a role in anteroposterior development that is partially redundant with Lim1
-
Zoltewicz, J. S., Plummer, N. W., Lin, M. I. and Peterson, A. S. (1999). oto is a homeotic locus with a role in anteroposterior development that is partially redundant with Lim1. Development 126, 5085-5095.
-
(1999)
Development
, vol.126
, pp. 5085-5095
-
-
Zoltewicz, J.S.1
Plummer, N.W.2
Lin, M.I.3
Peterson, A.S.4
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