-
1
-
-
0002844973
-
A history of the homeobox
-
Duboule D (ed) Oxford University Press, Oxford
-
Gehring WJ 1994 A history of the homeobox. In: Duboule D (ed) Guidebook to the Homeobox Genes. Oxford University Press, Oxford, pp 3-10
-
(1994)
Guidebook to the Homeobox Genes
, pp. 3-10
-
-
Gehring, W.J.1
-
3
-
-
0028561818
-
A class act: Conservation of homeodomain protein functions
-
Manak JR, Scott MP 1994 A class act: conservation of homeodomain protein functions. Development 1994, Suppl., 61-71
-
(1994)
Development 1994
, Issue.SUPPL.
, pp. 61-71
-
-
Manak, J.R.1
Scott, M.P.2
-
4
-
-
0028003107
-
The molecular architects of body design
-
McGinnis W, Kuziora M 1994 The molecular architects of body design. Sci Am 270:36-42
-
(1994)
Sci am
, vol.270
, pp. 36-42
-
-
McGinnis, W.1
Kuziora, M.2
-
5
-
-
0018240421
-
A gene complex controlling segmentation in Drosophila
-
Lewis EB 1978 A gene complex controlling segmentation in Drosophila. Nature 276:565-570
-
(1978)
Nature
, vol.276
, pp. 565-570
-
-
Lewis, E.B.1
-
6
-
-
0027932522
-
Colinearity and functional hierarchy among genes of the homeotic complexes
-
Duboule D, Morata G 1994 Colinearity and functional hierarchy among genes of the homeotic complexes. Trends Genet 10:358-364
-
(1994)
Trends Genet
, vol.10
, pp. 358-364
-
-
Duboule, D.1
Morata, G.2
-
7
-
-
0024328536
-
Altering the genome by homologous recombination
-
Capecchi MR 1989 Altering the genome by homologous recombination. Science 244:1288-1292
-
(1989)
Science
, vol.244
, pp. 1288-1292
-
-
Capecchi, M.R.1
-
8
-
-
0024283304
-
Transgenic animals
-
Jaenisch R 1988 Transgenic animals. Science 240:1468-1474
-
(1988)
Science
, vol.240
, pp. 1468-1474
-
-
Jaenisch, R.1
-
9
-
-
0025342695
-
Variations of cervical vertebrae after expression of a Hox-1:1 transgene in mice
-
Kessel M, Balling R, Gruss P 1990 Variations of cervical vertebrae after expression of a Hox-1:1 transgene in mice. Cell 61:301-308
-
(1990)
Cell
, vol.61
, pp. 301-308
-
-
Kessel, M.1
Balling, R.2
Gruss, P.3
-
10
-
-
0026497470
-
Homeotic transformation of the occipital bones of the skull by ectopic expression of a homeobox gene
-
Lufkin T, Mark M, Hart CP, Dollé P, LeMeur M, Chambon P 1992 Homeotic transformation of the occipital bones of the skull by ectopic expression of a homeobox gene. Nature 359:835-841
-
(1992)
Nature
, vol.359
, pp. 835-841
-
-
Lufkin, T.1
Mark, M.2
Hart, C.P.3
Dollé, P.4
LeMeur, M.5
Chambon, P.6
-
11
-
-
0030057027
-
Rescue of Drosophila labial null mutant by the chicken ortholog Hoxb-1 demonstrates that the function of Hox genes is phylogenetically conserved
-
Lutz B, Lu HC, Eichele G, Miller D, Kaufman TC 1996 Rescue of Drosophila labial null mutant by the chicken ortholog Hoxb-1 demonstrates that the function of Hox genes is phylogenetically conserved. Genes Dev 10:176-184
-
(1996)
Genes Dev
, vol.10
, pp. 176-184
-
-
Lutz, B.1
Lu, H.C.2
Eichele, G.3
Miller, D.4
Kaufman, T.C.5
-
12
-
-
0001028848
-
Alteration of Hox gene expression in the branchial region of the head causes homeotic transformations, hindbrain segmentation defects and atavistic changes
-
Mark M, Rijli FM, Chambon P 1995 Alteration of Hox gene expression in the branchial region of the head causes homeotic transformations, hindbrain segmentation defects and atavistic changes. Semin Dev Biol 6:275-284
-
(1995)
Semin Dev Biol
, vol.6
, pp. 275-284
-
-
Mark, M.1
Rijli, F.M.2
Chambon, P.3
-
13
-
-
0031062972
-
Developmental functions of mammalian Hox genes
-
Favier B, Dollé P 1997 Developmental functions of mammalian Hox genes. Mol Hum Reprod 3:115-131
-
(1997)
Mol Hum Reprod
, vol.3
, pp. 115-131
-
-
Favier, B.1
Dollé, P.2
-
14
-
-
0027375604
-
Mice homozygous for a targeted disruption of Hoxd-3 (Hox-4.1) exhibit anterior transformations of the first and second cervical vertebrae, the atlas and the axis
-
Condie BG, Capecchi MR 1993 Mice homozygous for a targeted disruption of Hoxd-3 (Hox-4.1) exhibit anterior transformations of the first and second cervical vertebrae, the atlas and the axis. Development 119:579-595
-
(1993)
Development
, vol.119
, pp. 579-595
-
-
Condie, B.G.1
Capecchi, M.R.2
-
15
-
-
0027189536
-
Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cervical vertebra and defects in the closure of the sternal rudiments
-
Ramirez-Solis R, Zheng H, Whiting J, Krumlauf R, Bradley A 1993 Hoxb-4 (Hox-2.6) mutant mice show homeotic transformation of a cervical vertebra and defects in the closure of the sternal rudiments. Cell 73:279-294
-
(1993)
Cell
, vol.73
, pp. 279-294
-
-
Ramirez-Solis, R.1
Zheng, H.2
Whiting, J.3
Krumlauf, R.4
Bradley, A.5
-
16
-
-
0026602808
-
Homeosis in the mouse induced by a null mutation in the Hox 3:1 gene
-
Le Mouellic H, Lallemand Y, Brûlet P 1992 Homeosis in the mouse induced by a null mutation in the Hox 3:1 gene. Cell 69:251-269
-
(1992)
Cell
, vol.69
, pp. 251-269
-
-
Le Mouellic, H.1
Lallemand, Y.2
Brûlet, P.3
-
17
-
-
0028921493
-
Axial skeleton homeosis and forelimb malformations in Hoxd-11 mutant mice
-
Favier B, LeMeur M, Chambon P, Dollé P 1995 Axial skeleton homeosis and forelimb malformations in Hoxd-11 mutant mice. Proc Natl Acad Sci USA 92:310-314
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 310-314
-
-
Favier, B.1
LeMeur, M.2
Chambon, P.3
Dollé, P.4
-
18
-
-
0030019608
-
Functional cooperation between the non-paralogous genes Hoxa-10 and Hoxd-11 in the developing forelimb and axial skeleton
-
Favier B, Rijli FM, Fromental-Ramain C, Fraulob V, Chambon P, Dollé P 1996 Functional cooperation between the non-paralogous genes Hoxa-10 and Hoxd-11 in the developing forelimb and axial skeleton. Development 122:449-460
-
(1996)
Development
, vol.122
, pp. 449-460
-
-
Favier, B.1
Rijli, F.M.2
Fromental-Ramain, C.3
Fraulob, V.4
Chambon, P.5
Dollé, P.6
-
19
-
-
0028124772
-
Mice with targeted disruption in the paralogous genes Hoxa-3 and Hoxd-3 reveal synergistic interaction
-
Condie BG, Capecchi MR 1994 Mice with targeted disruption in the paralogous genes Hoxa-3 and Hoxd-3 reveal synergistic interaction. Nature 370:304-307
-
(1994)
Nature
, vol.370
, pp. 304-307
-
-
Condie, B.G.1
Capecchi, M.R.2
-
20
-
-
0029143166
-
Compound mutants for the paralogous hoxa-4, hoxb-4, and hoxd-4 genes show more complete homeotic transformations and a dose-dependent increase in the number of vertebrae transformed
-
Horan GSB, Ramirez-Solis R, Featherstone MS, Wolgemuth DJ, Bradley A, Behringer RR 1995 Compound mutants for the paralogous hoxa-4, hoxb-4, and hoxd-4 genes show more complete homeotic transformations and a dose-dependent increase in the number of vertebrae transformed. Genes Dev 9:1667-1677
-
(1995)
Genes Dev
, vol.9
, pp. 1667-1677
-
-
Gsb, H.1
Ramirez-Solis, R.2
Featherstone, M.S.3
Wolgemuth, D.J.4
Bradley, A.5
Behringer, R.R.6
-
21
-
-
0030040552
-
Specific and redundant functions of the paralogous Hoxa-9 and Hoxd-9 genes in forelimb and axial skeleton patterning
-
Fromental-Ramain C, Warot X, Lakkaraju S, Favier B, Haack H, Birling C, Dierich A, Dollé P, Chambon P 1996 Specific and redundant functions of the paralogous Hoxa-9 and Hoxd-9 genes in forelimb and axial skeleton patterning. Development 122:461-472
-
(1996)
Development
, vol.122
, pp. 461-472
-
-
Fromental-Ramain, C.1
Warot, X.2
Lakkaraju, S.3
Favier, B.4
Haack, H.5
Birling, C.6
Dierich, A.7
Dollé, P.8
Chambon, P.9
-
22
-
-
0028859990
-
Genetic interaction between Hoxb-5 and Hoxb-6 revealed by nonallelic noncomplementation
-
Rancout DE, Tsuzuki T, Capecchi MR 1995 Genetic interaction between Hoxb-5 and Hoxb-6 revealed by nonallelic noncomplementation. Genes Dev 9:108-122
-
(1995)
Genes Dev
, vol.9
, pp. 108-122
-
-
Rancout, D.E.1
Tsuzuki, T.2
Capecchi, M.R.3
-
23
-
-
0025941823
-
Homeotic transformations of murine vertebrae and concomilant alteration of Hox codes induced by retinoic acid
-
Kessel M, Gruss P 1991 Homeotic transformations of murine vertebrae and concomilant alteration of Hox codes induced by retinoic acid. Cell 67:89-104
-
(1991)
Cell
, vol.67
, pp. 89-104
-
-
Kessel, M.1
Gruss, P.2
-
24
-
-
0026200238
-
Patterning in the vertebrate limb
-
Duboule D 1991 Patterning in the vertebrate limb. Curr Opin Gen Dev 1:211-216
-
(1991)
Curr Opin Gen Dev
, vol.1
, pp. 211-216
-
-
Duboule, D.1
-
25
-
-
0028085623
-
Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of Hoxd-11
-
Davis AP, Capecchi MR 1994 Axial homeosis and appendicular skeleton defects in mice with a targeted disruption of Hoxd-11. Development 120:2187-2198
-
(1994)
. Development
, vol.120
, pp. 2187-2198
-
-
Davis, A.P.1
Capecchi, M.R.2
-
26
-
-
0029963585
-
A mutational analysis of the 5′ HoxD genes: Dissection of genetic interactions during limb development in the mouse
-
Davis AP, Capecchi MR 1996 A mutational analysis of the 5′ HoxD genes: dissection of genetic interactions during limb development in the mouse. Development 122:1175-1185
-
(1996)
Development
, vol.122
, pp. 1175-1185
-
-
Davis, A.P.1
Capecchi, M.R.2
-
27
-
-
0027358721
-
Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs
-
Dollé P, Dierich A, LeMeur M, Schimmang T, Schuhbaur B, Chambon P, Duboule D 1993 Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs. Cell 75:431-441
-
(1993)
Cell
, vol.75
, pp. 431-441
-
-
Dollé, P.1
Dierich, A.2
Lemeur, M.3
Schimmang, T.4
Schuhbaur, B.5
Chambon, P.6
Duboule, D.7
-
28
-
-
0029851376
-
Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod
-
Fromental-Ramain C, Warot X, Messadecq N, LeMeur M, Dollé P, Chambon P 1996 Hoxa-13 and Hoxd-13 play a crucial role in the patterning of the limb autopod. Development 122:2997-3011
-
(1996)
Development
, vol.122
, pp. 2997-3011
-
-
Fromental-Ramain, C.1
Warot, X.2
Messadecq, N.3
LeMeur, M.4
Dollé, P.5
Chambon, P.6
-
29
-
-
0029026767
-
Absence of radius and ulna in mice lacking Hoxa-11 and Hoxd-11
-
Davis AP, Witte DP, Hsieh-Li HM, Potter SS, Capecchi MR 1995 Absence of radius and ulna in mice lacking Hoxa-11 and Hoxd-11. Nature 375:791-795
-
(1995)
Nature
, vol.375
, pp. 791-795
-
-
Davis, A.P.1
Witte, D.P.2
Hsieh-Li, H.M.3
Potter, S.S.4
Capecchi, M.R.5
-
30
-
-
0029871929
-
Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13
-
Muragaki Y, Mundlos S, Upton J, Olsen BR 1996 Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. Science 272:548-551
-
(1996)
Science
, vol.272
, pp. 548-551
-
-
Muragaki, Y.1
Mundlos, S.2
Upton, J.3
Olsen, B.R.4
-
31
-
-
0031050961
-
Mutation of HOXA13 in hand-foot-genital syndrome
-
Mortlock DP, Innis JW 1997 Mutation of HOXA13 in hand-foot-genital syndrome. Nat Genet 15:179-180
-
(1997)
Nat Genet
, vol.15
, pp. 179-180
-
-
Mortlock, D.P.1
Innis, J.W.2
-
32
-
-
0029854152
-
Synpolydactyly in mice with a targeted deficiency in the HoxD complex
-
Zákány J, Duboule D 1996 Synpolydactyly in mice with a targeted deficiency in the HoxD complex. Nature 384:69-71
-
(1996)
Nature
, vol.384
, pp. 69-71
-
-
Zákány, J.1
Duboule, D.2
-
33
-
-
0029160520
-
Cryptochidism and homeotic transformations of spinal nerves and vertebrae in Hoxa-10 mutant mice
-
Rijli F, Matyas R, Pellegrini M, Dierich A, Gruss P, Dollé P, Chambon P 1995 Cryptochidism and homeotic transformations of spinal nerves and vertebrae in Hoxa-10 mutant mice. Proc Natl Acad Sci USA 92:8185-8189
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 8185-8189
-
-
Rijli, F.1
Matyas, R.2
Pellegrini, M.3
Dierich, A.4
Gruss, P.5
Dollé, P.6
Chambon, P.7
-
34
-
-
0028926210
-
Sexually dimorphic sterility phenotypes in Hoxa-10 deficient mice
-
Satokata I, Benson G, Maas R 1995 Sexually dimorphic sterility phenotypes in Hoxa-10 deficient mice. Nature 374:460-463
-
(1995)
Nature
, vol.374
, pp. 460-463
-
-
Satokata, I.1
Benson, G.2
Maas, R.3
-
35
-
-
0029793280
-
Mechanisms of reduced fertility in Hoxa-10 mutant mice: Uterine homeosis and loss of maternal Hoxa-10 expression
-
Benson GV, Lim H, Paria BC, Satokata I, Dey SK, Maas RL 1996 Mechanisms of reduced fertility in Hoxa-10 mutant mice: uterine homeosis and loss of maternal Hoxa-10 expression. Development 122:2687-2696
-
(1996)
Development
, vol.122
, pp. 2687-2696
-
-
Benson, G.V.1
Lim, H.2
Paria, B.C.3
Satokata, I.4
Dey, S.K.5
Maas, R.L.6
-
36
-
-
0029069318
-
Hoxa-11 structure, extensive antisence transcription, and function in male and female fertility
-
Hsieh-Li HM, Witte DP, Weinstein M, Branford W, Li H, Small K, Potter SS 1995 Hoxa-11 structure, extensive antisence transcription, and function in male and female fertility. Development 121:1373-1385
-
(1995)
Development
, vol.121
, pp. 1373-1385
-
-
Hsieh-Li, H.M.1
Witte, D.P.2
Weinstein, M.3
Branford, W.4
Li, H.5
Small, K.6
Potter, S.S.7
-
37
-
-
0029835646
-
Function of posterior HoxD genes in the morphogenesis of the anal sphincter
-
Kondo T, Dollé P, Zákány J, Duboule D 1996 Function of posterior HoxD genes in the morphogenesis of the anal sphincter. Development 122:2651-2659
-
(1996)
Development
, vol.122
, pp. 2651-2659
-
-
Kondo, T.1
Dollé, P.2
Zákány, J.3
Duboule, D.4
-
38
-
-
0025271329
-
Segmentation and the origin of regional diversity in the vertebrate central nervous system
-
Keynes R, Lumsden A 1990 Segmentation and the origin of regional diversity in the vertebrate central nervous system. Neuron 4:1-9
-
(1990)
Neuron
, vol.4
, pp. 1-9
-
-
Keynes, R.1
Lumsden, A.2
-
39
-
-
0027413198
-
Hox genes and pattern formation in the branchial region of the vertebrate head
-
Krumlauf R 1993 Hox genes and pattern formation in the branchial region of the vertebrate head. Trends Genet 9:106-112
-
(1993)
Trends Genet
, vol.9
, pp. 106-112
-
-
Krumlauf, R.1
-
40
-
-
0027739813
-
A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene
-
Rijli FM, Mark M, Lakkaraju S, Dierich A, Dollé P, Chambon P 1993 A homeotic transformation is generated in the rostral branchial region of the head by disruption of Hoxa-2, which acts as a selector gene. Cell 75:1333-1349
-
(1993)
Cell
, vol.75
, pp. 1333-1349
-
-
Rijli, F.M.1
Mark, M.2
Lakkaraju, S.3
Dierich, A.4
Dollé, P.5
Chambon, P.6
-
41
-
-
0027759447
-
Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest
-
Gendron-Maguire M, Mallo M, Zhang M, Gridley T 1993 Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest. Cell 75:1317-1331
-
(1993)
Cell
, vol.75
, pp. 1317-1331
-
-
Gendron-Maguire, M.1
Mallo, M.2
Zhang, M.3
Gridley, T.4
-
42
-
-
0029030722
-
The role of Hoxa-3 in mouse thymus and thyroid development
-
Manley NR, Capecchi MR 1995 The role of Hoxa-3 in mouse thymus and thyroid development. Development 121:1989-2003
-
(1995)
Development
, vol.121
, pp. 1989-2003
-
-
Manley, N.R.1
Capecchi, M.R.2
-
43
-
-
15844403609
-
A common region of 10p deleted in DiGeorge and velocardiofacial syndromes
-
Daw SCM, Taylor C, Kraman M, Call K, Mao J, Schulfenhauer S, Meitinger T, Lipson T, Goodship J, Scambler P 1996 A common region of 10p deleted in DiGeorge and velocardiofacial syndromes. Nat Genet 13:458-460
-
(1996)
Nat Genet
, vol.13
, pp. 458-460
-
-
Daw, S.C.M.1
Taylor, C.2
Kraman, M.3
Call, K.4
Mao, J.5
Schulfenhauer, S.6
Meitinger, T.7
Lipson, T.8
Goodship, J.9
Scambler, P.10
-
44
-
-
0027384351
-
Two rhombomeres are altered in Hoxa-1 mutant mice
-
Mark M, Lufkin T, Vonesch JL, Ruberte E, Olivo JC, Dollé P, Gorry P, Lumsden A, Chambon P 1993 Two rhombomeres are altered in Hoxa-1 mutant mice. Development 119:319-388
-
(1993)
Development
, vol.119
, pp. 319-388
-
-
Mark, M.1
Lufkin, T.2
Vonesch, J.L.3
Ruberte, E.4
Olivo, J.C.5
Dollé, P.6
Gorry, P.7
Lumsden, A.8
Chambon, P.9
-
45
-
-
0027249799
-
Loss of Hoxa-1 (Hox-1.6) function results in the reorganization of the murine hindbrain
-
Carpenter EM, Goddard JM, Chisaka O, Manley NR, Capecchi MR 1993 Loss of Hoxa-1 (Hox-1.6) function results in the reorganization of the murine hindbrain. Development 118:1063-1075
-
(1993)
Development
, vol.118
, pp. 1063-1075
-
-
Carpenter, E.M.1
Goddard, J.M.2
Chisaka, O.3
Manley, N.R.4
Capecchi, M.R.5
-
46
-
-
0029824070
-
Mice with targeted disruption of Hoxb-1 fail to form the motor nucleus of the VIIth nerve
-
Goddard JM, Rossel M, Manley NR, Capecchi MR 1996 Mice with targeted disruption of Hoxb-1 fail to form the motor nucleus of the VIIth nerve. Development 122:3217-3228
-
(1996)
Development
, vol.122
, pp. 3217-3228
-
-
Goddard, J.M.1
Rossel, M.2
Manley, N.R.3
Capecchi, M.R.4
-
47
-
-
0030447736
-
Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1
-
Studer M, Lumsden A, Ariza-McNaughton L, Bradley A, Krumlauf R 1996 Altered segmental identity and abnormal migration of motor neurons in mice lacking Hoxb-1. Nature 384:630-634
-
(1996)
Nature
, vol.384
, pp. 630-634
-
-
Studer, M.1
Lumsden, A.2
Ariza-McNaughton, L.3
Bradley, A.4
Krumlauf, R.5
-
48
-
-
0030481054
-
Targeted disruption of the Hoxb-2 locus in mice interferes with expression of Hoxb-1 and Hoxh-4
-
Barrow JR, Capecchi MR 1996 Targeted disruption of the Hoxb-2 locus in mice interferes with expression of Hoxb-1 and Hoxh-4. Development 122:3817-3828
-
(1996)
Development
, vol.122
, pp. 3817-3828
-
-
Barrow, J.R.1
Capecchi, M.R.2
-
49
-
-
0027982374
-
From fly head to mammalian forebrain: The story of otd and Otx
-
Finkelstein R, Boncinelli E 1994 From fly head to mammalian forebrain: the story of otd and Otx. Trends Genet 10:310-315
-
(1994)
Trends Genet
, vol.10
, pp. 310-315
-
-
Finkelstein, R.1
Boncinelli, E.2
-
50
-
-
0028807157
-
Forebrain and midbrain regions are deleted in Otx2-/- Mutants due to a defective anterior neurectoderm specification during gastrulation
-
Acampora D Mazan, S., Lallemand, Y., Avantaggiato, V., Maury, M., Simeone, A., Brûlet, P. 1995 Forebrain and midbrain regions are deleted in Otx2-/- mutants due to a defective anterior neurectoderm specification during gastrulation. Development 121:3279-3290
-
(1995)
Development
, vol.121
, pp. 3279-3290
-
-
Acampora D Mazan, S.1
Lallemand, Y.2
Avantaggiato, V.3
Maury, M.4
Simeone, A.5
Brûlet, P.6
-
51
-
-
0030050751
-
A targeted mouse Otx-2 mutation leads to severe defects in gastrulation and formation of axial mesoderm and to deletion of rostral brain
-
Ang SL, Jin O, Rhinn M, Daigle N, Stevenson L, Rossant J 1996 A targeted mouse Otx-2 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
-
52
-
-
0030482082
-
Dentate gyrus formation requires Emx2
-
Pellegrini, M., Mansouri, A., Simeone, A., Boncinelli, E., Gruss, P. 1996 Dentate gyrus formation requires Emx2 Development 122:3893-3898
-
(1996)
Development
, vol.122
, pp. 3893-3898
-
-
Pellegrini, M.1
Mansouri, A.2
Simeone, A.3
Boncinelli, E.4
Gruss, P.5
-
53
-
-
0030065606
-
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
-
V
-
Brunelli S, Faiella A, Capra V, Nigro V, Simeone A, Cama A, V Boncinelli E 1996 Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Nat Genet 12:94-96
-
(1996)
Nat Genet
, vol.12
, pp. 94-96
-
-
Brunelli, S.1
Faiella, A.2
Capra, V.3
Nigro, V.4
Simeone, A.5
Cama, A.6
Boncinelli, E.7
-
54
-
-
0029820548
-
Epilepsy and brain abnormalities in mice lacking the Otx1 gene
-
Acampora D, Mazan S, Avantaggiato V, Barone P, Tuorto F, Lallemand Y, Brûlet P, Simeone A 1996 Epilepsy and brain abnormalities in mice lacking the Otx1 gene. Nat Genet 14:218-222
-
(1996)
Nat Genet
, vol.14
, pp. 218-222
-
-
Acampora, D.1
Mazan, S.2
Avantaggiato, V.3
Barone, P.4
Tuorto, F.5
Lallemand, Y.6
Brûlet, P.7
Simeone, A.8
-
55
-
-
0029059790
-
Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2
-
Hanks M, Wurst W, Anson-Cartwright L, Auerbach AB, Joyner AL 1995 Rescue of the En-1 mutant phenotype by replacement of En-1 with En-2. Science 269:679-682
-
(1995)
Science
, vol.269
, pp. 679-682
-
-
Hanks, M.1
Wurst, W.2
Anson-Cartwright, L.3
Auerbach, A.B.4
Joyner, A.L.5
-
57
-
-
0028074973
-
PAX6 gene dosage effect in a family with congenital cataracts, anophthalmia and central nervous system defects
-
Glaser T, Jepeal L, Edwards JG, Young SR, Favor J, Maas RL 1994 PAX6 gene dosage effect in a family with congenital cataracts, anophthalmia and central nervous system defects. Nat Genet 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
-
58
-
-
0030162151
-
PAX6 missense mutation in isolated foveal hypoplasia
-
Azuma N, Nishina S, Yanagisawa H, Okuyama T, Yamada M 1996 PAX6 missense mutation in isolated foveal hypoplasia. Nat Genet 13:141-142
-
(1996)
Nat Genet
, vol.13
, pp. 141-142
-
-
Azuma, N.1
Nishina, S.2
Yanagisawa, H.3
Okuyama, T.4
Yamada, M.5
-
60
-
-
0030560840
-
Tooth morphogenesis and cell differentiation
-
Thesleff I, Nieminen P 1996 Tooth morphogenesis and cell differentiation. Current Opin Cell Biol 8:844-850
-
(1996)
Current Opin Cell Biol
, vol.8
, pp. 844-850
-
-
Thesleff, I.1
Nieminen, P.2
-
61
-
-
0029188387
-
Homeobox genes in orofacial development
-
Sharpe PT 1995 Homeobox genes in orofacial development. Connect Tissue Res 32:17-25
-
(1995)
Connect Tissue Res
, vol.32
, pp. 17-25
-
-
Sharpe, P.T.1
-
62
-
-
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 WLM, Small KW, Datson NA, Siegel-Bartelt J, Bierke-Nelson D, Bitoun P, Zabel BU, Carey JC, Murray JC 1996 Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome. Nat Genet 14:392-399
-
(1996)
Nat Genet
, vol.14
, pp. 392-399
-
-
Semina, E.V.1
Reiter, R.2
Leysens, N.J.3
Wlm, A.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
-
63
-
-
0029278635
-
Craniofacial genetics makes headway
-
Richman JM 1995 Craniofacial genetics makes headway. Curr Biol 5:345-348
-
(1995)
Curr Biol
, vol.5
, pp. 345-348
-
-
Richman, J.M.1
-
64
-
-
0028138679
-
Transcriptional mechanisms in anterior pituitary cell differentiation
-
Rhodes SJ, DiMattia GE, Rosenfeld MG 1994 Transcriptional mechanisms in anterior pituitary cell differentiation. Curr Opin Genet Dev 4:709-717
-
(1994)
Curr Opin Genet Dev
, vol.4
, pp. 709-717
-
-
Rhodes, S.J.1
DiMattia, G.E.2
Rosenfeld, M.G.3
-
65
-
-
0028988233
-
Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4
-
Kok YJM, van der Maarel SM, Bitner-Glindzicz M, Huber I, Monaco AP, Malcolm S, Pembrey ME, Ropers HH, Cremers FPM 1995 Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4. Science 267:685-688
-
(1995)
Science
, vol.267
, pp. 685-688
-
-
Yjm, K.1
Van Der Maarel, S.M.2
Bitner-Glindzicz, M.3
Huber, I.4
Monaco, A.P.5
Malcolm, S.6
Pembrey, M.E.7
Ropers, H.H.8
Cremers, F.P.M.9
-
67
-
-
0030034673
-
Cooperative activation of Hoxa and Pbx1-related genes in murine myeloid leukaemias
-
Nakamura T, Largaespada DA, Shaughnessy JD Jr, Jenkins NA, Copeland NG 1996 Cooperative activation of Hoxa and Pbx1-related genes in murine myeloid leukaemias. Nat Genet 12:149-153
-
(1996)
Nat Genet
, vol.12
, pp. 149-153
-
-
Nakamura, T.1
Largaespada, D.A.2
Shaughnessy J.D., Jr.3
Jenkins, N.A.4
Copeland, N.G.5
-
68
-
-
0028869112
-
Altered Hox expression and segmental identity in Mll-mutant mice
-
Yu BD, Hess JL, Horning SE, Brown GAJ, Korsmeyer SJ 1995 Altered Hox expression and segmental identity in Mll-mutant mice. Nature 378:505-508
-
(1995)
Nature
, vol.378
, pp. 505-508
-
-
Yu, B.D.1
Hess, J.L.2
Horning, S.E.3
Gaj, B.4
Korsmeyer, S.J.5
-
69
-
-
0029990114
-
Gene fusions encoding chimaeric transcription factors in solid tumours
-
Sorensen PHB, Triche TJ 1996 Gene fusions encoding chimaeric transcription factors in solid tumours. Semin Cancer Biol 7:3-14
-
(1996)
Semin Cancer Biol
, vol.7
, pp. 3-14
-
-
Sorensen, P.H.B.1
Triche, T.J.2
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