-
1
-
-
0036111153
-
Planar signaling and morphogenesis in Drosophila
-
Adler P.N. Planar signaling and morphogenesis in Drosophila. Dev. Cell 2 (2002) 525-535
-
(2002)
Dev. Cell
, vol.2
, pp. 525-535
-
-
Adler, P.N.1
-
2
-
-
0034161298
-
Finding the genes that direct mammalian development: ENU mutagenesis in the mouse
-
Anderson K.V. Finding the genes that direct mammalian development: ENU mutagenesis in the mouse. Trends Genet. 16 (2000) 99-102
-
(2000)
Trends Genet.
, vol.16
, pp. 99-102
-
-
Anderson, K.V.1
-
3
-
-
84981841769
-
Analysis of teh developmental effects of a lethal mutation in the house mouse
-
Auerbach R. Analysis of teh developmental effects of a lethal mutation in the house mouse. J. Exp. Zool. 127 (1954) 305-329
-
(1954)
J. Exp. Zool.
, vol.127
, pp. 305-329
-
-
Auerbach, R.1
-
4
-
-
0029638071
-
Possible homozygous Waardenburg syndrome in a fetus with exencephaly
-
Ayme S., and Philip N. Possible homozygous Waardenburg syndrome in a fetus with exencephaly. Am. J. Med. Genet. 59 (1995) 263-265
-
(1995)
Am. J. Med. Genet.
, vol.59
, pp. 263-265
-
-
Ayme, S.1
Philip, N.2
-
5
-
-
0024277960
-
Undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1
-
Balling R., et al. Undulated, a mutation affecting the development of the mouse skeleton, has a point mutation in the paired box of Pax 1. Cell 55 (1988) 531-535
-
(1988)
Cell
, vol.55
, pp. 531-535
-
-
Balling, R.1
-
6
-
-
18344389337
-
Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator
-
Bamforth S.D., et al. Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator. Nat. Genet. 29 (2001) 469-474
-
(2001)
Nat. Genet.
, vol.29
, pp. 469-474
-
-
Bamforth, S.D.1
-
7
-
-
0036471326
-
Folic acid prevents exencephaly in Cited2 deficient mice
-
Barbera J.P., et al. Folic acid prevents exencephaly in Cited2 deficient mice. Hum. Mol. Genet. 11 (2002) 283-293
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 283-293
-
-
Barbera, J.P.1
-
9
-
-
0034628471
-
Localization of apical epithelial determinants by the basolateral PDZ protein Scribble
-
Bilder D., and Perrimon N. Localization of apical epithelial determinants by the basolateral PDZ protein Scribble. Nature 403 (2000) 676-680
-
(2000)
Nature
, vol.403
, pp. 676-680
-
-
Bilder, D.1
Perrimon, N.2
-
10
-
-
0037076403
-
Epidermolysis bullosa and embryonic lethality in mice lacking the multi-PDZ domain protein GRIP1
-
Bladt F., et al. Epidermolysis bullosa and embryonic lethality in mice lacking the multi-PDZ domain protein GRIP1. Proc. Natl Acad. Sci. USA 99 (2002) 6816-6821
-
(2002)
Proc. Natl Acad. Sci. USA
, vol.99
, pp. 6816-6821
-
-
Bladt, F.1
-
11
-
-
33747588534
-
Neural tube defects and folate: Case far from closed
-
Blom H.J., et al. Neural tube defects and folate: Case far from closed. Nat. Rev. Neurosci. 7 (2006) 724-731
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 724-731
-
-
Blom, H.J.1
-
12
-
-
8444232068
-
New semidominant mutations that affect mouse development
-
Bogani D., et al. New semidominant mutations that affect mouse development. Genesis 40 (2004) 109-117
-
(2004)
Genesis
, vol.40
, pp. 109-117
-
-
Bogani, D.1
-
13
-
-
17844393354
-
Candidate gene analysis in human neural tube defects
-
Boyles A.L., et al. Candidate gene analysis in human neural tube defects. Am. J. Med. Genet. C Semin. Med. Genet. 135C (2005) 9-23
-
(2005)
Am. J. Med. Genet. C Semin. Med. Genet.
, vol.135 C
, pp. 9-23
-
-
Boyles, A.L.1
-
14
-
-
0025947203
-
Curvature of the caudal region is responsible for failure of neural tube closure in the curly tail (ct) mouse embryo
-
Brook F.A., et al. Curvature of the caudal region is responsible for failure of neural tube closure in the curly tail (ct) mouse embryo. Development 113 (1991) 671-678
-
(1991)
Development
, vol.113
, pp. 671-678
-
-
Brook, F.A.1
-
15
-
-
20144387120
-
Toward positional cloning of the curly tail gene
-
Brouns M.R., et al. Toward positional cloning of the curly tail gene. Birth Defects Res. A Clin. Mol. Teratol. 73 (2005) 154-161
-
(2005)
Birth Defects Res. A Clin. Mol. Teratol.
, vol.73
, pp. 154-161
-
-
Brouns, M.R.1
-
16
-
-
0034502484
-
A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes
-
Bultman S., et al. A Brg1 null mutation in the mouse reveals functional differences among mammalian SWI/SNF complexes. Mol. Cell 6 (2000) 1287-1295
-
(2000)
Mol. Cell
, vol.6
, pp. 1287-1295
-
-
Bultman, S.1
-
17
-
-
13444271008
-
Investigations into the etiology of neural tube defects
-
Cabrera R.M., et al. Investigations into the etiology of neural tube defects. Birth Defects Res. C Embryo Today 72 (2004) 330-344
-
(2004)
Birth Defects Res. C Embryo Today
, vol.72
, pp. 330-344
-
-
Cabrera, R.M.1
-
18
-
-
0026583899
-
Waardenburg syndrome associated with meningomyelocele
-
Carezani-Gavin M., et al. Waardenburg syndrome associated with meningomyelocele. Am. J. Med. Genet. 42 (1992) 135-136
-
(1992)
Am. J. Med. Genet.
, vol.42
, pp. 135-136
-
-
Carezani-Gavin, M.1
-
19
-
-
0141570875
-
Cordon-bleu is a conserved gene involved in neural tube formation
-
Carroll E.A., et al. Cordon-bleu is a conserved gene involved in neural tube formation. Dev. Biol. 262 (2003) 16-31
-
(2003)
Dev. Biol.
, vol.262
, pp. 16-31
-
-
Carroll, E.A.1
-
20
-
-
33748312252
-
Uncovering the uncharacterized and unexpected: Unbiased phenotype-driven screens in the mouse
-
Caspary T., and Anderson K.V. Uncovering the uncharacterized and unexpected: Unbiased phenotype-driven screens in the mouse. Dev. Dyn. 235 (2006) 2412-2423
-
(2006)
Dev. Dyn.
, vol.235
, pp. 2412-2423
-
-
Caspary, T.1
Anderson, K.V.2
-
21
-
-
0037125938
-
Mouse dispatched homolog1 is required for long-range, but not juxtacrine, Hh signaling
-
Caspary T., et al. Mouse dispatched homolog1 is required for long-range, but not juxtacrine, Hh signaling. Curr. Biol. 12 (2002) 1628-1632
-
(2002)
Curr. Biol.
, vol.12
, pp. 1628-1632
-
-
Caspary, T.1
-
22
-
-
34247558062
-
The graded response to Sonic Hedgehog depends on cilia architecture
-
Caspary T., et al. The graded response to Sonic Hedgehog depends on cilia architecture. Dev. Cell 12 (2007) 767-778
-
(2007)
Dev. Cell
, vol.12
, pp. 767-778
-
-
Caspary, T.1
-
23
-
-
0033961243
-
Increased mRNA levels of Mn-SOD and catalase in embryos of diabetic rats from a malformation-resistant strain
-
Cederberg J., et al. Increased mRNA levels of Mn-SOD and catalase in embryos of diabetic rats from a malformation-resistant strain. Diabetes 49 (2000) 101-107
-
(2000)
Diabetes
, vol.49
, pp. 101-107
-
-
Cederberg, J.1
-
24
-
-
0036723816
-
Maternal diabetes increases the risk of caudal regression caused by retinoic acid
-
Chan B.W., et al. Maternal diabetes increases the risk of caudal regression caused by retinoic acid. Diabetes 51 (2002) 2811-2816
-
(2002)
Diabetes
, vol.51
, pp. 2811-2816
-
-
Chan, B.W.1
-
25
-
-
0037955858
-
Oxidant regulation of gene expression and neural tube development: Insights gained from diabetic pregnancy on molecular causes of neural tube defects
-
Chang T.I., et al. Oxidant regulation of gene expression and neural tube development: Insights gained from diabetic pregnancy on molecular causes of neural tube defects. Diabetologia 46 (2003) 538-545
-
(2003)
Diabetologia
, vol.46
, pp. 538-545
-
-
Chang, T.I.1
-
27
-
-
0027407062
-
Waardenburg syndrome and myelomeningocele in a family
-
Chatkupt S., et al. Waardenburg syndrome and myelomeningocele in a family. J. Med. Genet. 30 (1993) 83-84
-
(1993)
J. Med. Genet.
, vol.30
, pp. 83-84
-
-
Chatkupt, S.1
-
28
-
-
0028206583
-
Prevention of spinal neural tube defects in the curly tail mouse mutant by a specific effect of retinoic acid
-
Chen W.H., et al. Prevention of spinal neural tube defects in the curly tail mouse mutant by a specific effect of retinoic acid. Dev. Dyn. 199 (1994) 93-102
-
(1994)
Dev. Dyn.
, vol.199
, pp. 93-102
-
-
Chen, W.H.1
-
29
-
-
0029777408
-
Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
-
Chiang C., et al. Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function. Nature 383 (1996) 407-413
-
(1996)
Nature
, vol.383
, pp. 407-413
-
-
Chiang, C.1
-
30
-
-
0346656870
-
Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol
-
Cogram P., et al. Specific isoforms of protein kinase C are essential for prevention of folate-resistant neural tube defects by inositol. Hum. Mol. Genet. 13 (2004) 7-14
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 7-14
-
-
Cogram, P.1
-
31
-
-
0022273459
-
Relationship between timing of posterior neuropore closure and development of spinal neural tube defects in mutant (curly tail) and normal mouse embryos in culture
-
Copp A.J. Relationship between timing of posterior neuropore closure and development of spinal neural tube defects in mutant (curly tail) and normal mouse embryos in culture. J. Embryol. Exp. Morphol. 88 (1985) 39-54
-
(1985)
J. Embryol. Exp. Morphol.
, vol.88
, pp. 39-54
-
-
Copp, A.J.1
-
32
-
-
0020002198
-
Neural tube development in mutant (curly tail) and normal mouse embryos: The timing of posterior neuropore closure in vivo and in vitro
-
Copp A.J., et al. Neural tube development in mutant (curly tail) and normal mouse embryos: The timing of posterior neuropore closure in vivo and in vitro. J. Embryol. Exp. Morphol. 69 (1982) 151-167
-
(1982)
J. Embryol. Exp. Morphol.
, vol.69
, pp. 151-167
-
-
Copp, A.J.1
-
33
-
-
0023709064
-
A cell-type-specific abnormality of cell proliferation in mutant (curly tail) mouse embryos developing spinal neural tube defects
-
Copp A.J., et al. A cell-type-specific abnormality of cell proliferation in mutant (curly tail) mouse embryos developing spinal neural tube defects. Development 104 (1988) 285-295
-
(1988)
Development
, vol.104
, pp. 285-295
-
-
Copp, A.J.1
-
34
-
-
0023736270
-
Prevention of spinal neural tube defects in the mouse embryo by growth retardation during neurulation
-
Copp A.J., et al. Prevention of spinal neural tube defects in the mouse embryo by growth retardation during neurulation. Development 104 (1988) 297-303
-
(1988)
Development
, vol.104
, pp. 297-303
-
-
Copp, A.J.1
-
35
-
-
0028040705
-
Developmental basis of severe neural tube defects in the loop-tail (Lp) mutant mouse: Use of microsatellite DNA markers to identify embryonic genotype
-
Copp A.J., et al. Developmental basis of severe neural tube defects in the loop-tail (Lp) mutant mouse: Use of microsatellite DNA markers to identify embryonic genotype. Dev. Biol. 165 (1994) 20-29
-
(1994)
Dev. Biol.
, vol.165
, pp. 20-29
-
-
Copp, A.J.1
-
36
-
-
0141483382
-
The genetic basis of mammalian neurulation
-
Copp A.J., et al. The genetic basis of mammalian neurulation. Nat. Rev. Genet. 4 (2003) 784-793
-
(2003)
Nat. Rev. Genet.
, vol.4
, pp. 784-793
-
-
Copp, A.J.1
-
37
-
-
26644460824
-
Vertebrate Smoothened functions at the primary cilium
-
Corbit K.C., et al. Vertebrate Smoothened functions at the primary cilium. Nature 437 (2005) 1018-1021
-
(2005)
Nature
, vol.437
, pp. 1018-1021
-
-
Corbit, K.C.1
-
38
-
-
0025346389
-
The induction of tail malformations in trisomy 16 mouse fetuses heterozygous for the curly tail recessive gene
-
Crolla J.A., et al. The induction of tail malformations in trisomy 16 mouse fetuses heterozygous for the curly tail recessive gene. Genet. Res. 55 (1990) 27-32
-
(1990)
Genet. Res.
, vol.55
, pp. 27-32
-
-
Crolla, J.A.1
-
39
-
-
10744227509
-
Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse
-
Curtin J.A., et al. Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse. Curr. Biol. 13 (2003) 1129-1133
-
(2003)
Curr. Biol.
, vol.13
, pp. 1129-1133
-
-
Curtin, J.A.1
-
40
-
-
0025912634
-
Waardenburg I syndrome: A clinical and genetic study of two large Brazilian kindreds, and literature review
-
da-Silva E.O. Waardenburg I syndrome: A clinical and genetic study of two large Brazilian kindreds, and literature review. Am. J. Med. Genet. 40 (1991) 65-74
-
(1991)
Am. J. Med. Genet.
, vol.40
, pp. 65-74
-
-
da-Silva, E.O.1
-
41
-
-
33846646986
-
The Meckel-Gruber syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation
-
Dawe H.R., et al. The Meckel-Gruber syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation. Hum. Mol. Genet. 16 (2007) 173-186
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 173-186
-
-
Dawe, H.R.1
-
42
-
-
34347324031
-
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
-
Delous M., et al. The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome. Nat. Genet. 39 (2007) 875-881
-
(2007)
Nat. Genet.
, vol.39
, pp. 875-881
-
-
Delous, M.1
-
43
-
-
33750039987
-
Current perspectives on the genetic causes of neural tube defects
-
De Marco P., et al. Current perspectives on the genetic causes of neural tube defects. Neurogenetics 7 (2006) 201-221
-
(2006)
Neurogenetics
, vol.7
, pp. 201-221
-
-
De Marco, P.1
-
44
-
-
0021146433
-
Waardenburg syndrome in South Africa. Part I. An evaluation of the clinical findings in 11 families
-
de Saxe M., et al. Waardenburg syndrome in South Africa. Part I. An evaluation of the clinical findings in 11 families. S. Afr. Med. J. 66 (1984) 256-261
-
(1984)
S. Afr. Med. J.
, vol.66
, pp. 256-261
-
-
de Saxe, M.1
-
45
-
-
20444424616
-
Human neural tube defects: Developmental biology, epidemiology, and genetics
-
Detrait E.R., et al. Human neural tube defects: Developmental biology, epidemiology, and genetics. Neurotoxicol. Teratol. 27 (2005) 515-524
-
(2005)
Neurotoxicol. Teratol.
, vol.27
, pp. 515-524
-
-
Detrait, E.R.1
-
46
-
-
0024292631
-
Pax 1, a member of a paired box homologous murine gene family, is expressed in segmented structures during development
-
Deutsch U., et al. Pax 1, a member of a paired box homologous murine gene family, is expressed in segmented structures during development. Cell 53 (1988) 617-625
-
(1988)
Cell
, vol.53
, pp. 617-625
-
-
Deutsch, U.1
-
47
-
-
21644443932
-
Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients
-
Doudney K., et al. Analysis of the planar cell polarity gene Vangl2 and its co-expressed paralogue Vangl1 in neural tube defect patients. Am. J. Med. Genet. A 136 (2005) 90-92
-
(2005)
Am. J. Med. Genet. A
, vol.136
, pp. 90-92
-
-
Doudney, K.1
-
49
-
-
0035849901
-
Rab23 is an essential negative regulator of the mouse Sonic hedgehog signalling pathway
-
Eggenschwiler J.T., et al. Rab23 is an essential negative regulator of the mouse Sonic hedgehog signalling pathway. Nature 412 (2001) 194-198
-
(2001)
Nature
, vol.412
, pp. 194-198
-
-
Eggenschwiler, J.T.1
-
50
-
-
0025855806
-
Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1
-
Epstein D.J., et al. Molecular characterization of a deletion encompassing the splotch mutation on mouse chromosome 1. Genomics 10 (1991) 89-93
-
(1991)
Genomics
, vol.10
, pp. 89-93
-
-
Epstein, D.J.1
-
51
-
-
0025925068
-
Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
-
Epstein D.J., et al. Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3. Cell 67 (1991) 767-774
-
(1991)
Cell
, vol.67
, pp. 767-774
-
-
Epstein, D.J.1
-
52
-
-
0027393598
-
A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant
-
Epstein D.J., et al. A mutation within intron 3 of the Pax-3 gene produces aberrantly spliced mRNA transcripts in the splotch (Sp) mouse mutant. Proc. Natl Acad. Sci. USA 90 (1993) 532-536
-
(1993)
Proc. Natl Acad. Sci. USA
, vol.90
, pp. 532-536
-
-
Epstein, D.J.1
-
53
-
-
0027323660
-
Interaction between splotch (Sp) and curly tail (ct) mouse mutants in the embryonic development of neural tube defects
-
Estibeiro J.P., et al. Interaction between splotch (Sp) and curly tail (ct) mouse mutants in the embryonic development of neural tube defects. Development 119 (1993) 113-121
-
(1993)
Development
, vol.119
, pp. 113-121
-
-
Estibeiro, J.P.1
-
54
-
-
0028630689
-
Patterning of mammalian somites by surface ectoderm and notochord: Evidence for sclerotome induction by a hedgehog homolog
-
Fan C.M., and Tessier-Lavigne M. Patterning of mammalian somites by surface ectoderm and notochord: Evidence for sclerotome induction by a hedgehog homolog. Cell 79 (1994) 1175-1186
-
(1994)
Cell
, vol.79
, pp. 1175-1186
-
-
Fan, C.M.1
Tessier-Lavigne, M.2
-
55
-
-
0033513480
-
Evidence that elevated glucose causes altered gene expression, apoptosis, and neural tube defects in a mouse model of diabetic pregnancy
-
Fine E.L., et al. Evidence that elevated glucose causes altered gene expression, apoptosis, and neural tube defects in a mouse model of diabetic pregnancy. Diabetes 48 (1999) 2454-2462
-
(1999)
Diabetes
, vol.48
, pp. 2454-2462
-
-
Fine, E.L.1
-
56
-
-
0037636320
-
Pathobiology and genetics of neural tube defects
-
Finnell R.H., et al. Pathobiology and genetics of neural tube defects. Epilepsia 44 Suppl. 3 (2003) 14-23
-
(2003)
Epilepsia
, vol.44
, Issue.SUPPL. 3
, pp. 14-23
-
-
Finnell, R.H.1
-
57
-
-
0032568871
-
Embryonic folate metabolism and mouse neural tube defects
-
Fleming A., and Copp A.J. Embryonic folate metabolism and mouse neural tube defects. Science 280 (1998) 2107-2109
-
(1998)
Science
, vol.280
, pp. 2107-2109
-
-
Fleming, A.1
Copp, A.J.2
-
58
-
-
38149045761
-
Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome
-
Frank V., et al. Mutations of the CEP290 gene encoding a centrosomal protein cause Meckel-Gruber syndrome. Hum. Mutat. 29 (2008) 45-52
-
(2008)
Hum. Mutat.
, vol.29
, pp. 45-52
-
-
Frank, V.1
-
59
-
-
0033152690
-
Notochord-dependent expression of MFH1 and PAX1 cooperates to maintain the proliferation of sclerotome cells during the vertebral column development
-
Furumoto T.A., et al. Notochord-dependent expression of MFH1 and PAX1 cooperates to maintain the proliferation of sclerotome cells during the vertebral column development. Dev. Biol. 210 (1999) 15-29
-
(1999)
Dev. Biol.
, vol.210
, pp. 15-29
-
-
Furumoto, T.A.1
-
60
-
-
20944433211
-
Analysis of mouse embryonic patterning and morphogenesis by forward genetics
-
Garcia-Garcia M.J., et al. Analysis of mouse embryonic patterning and morphogenesis by forward genetics. Proc. Natl Acad. Sci. USA 102 (2005) 5913-5919
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 5913-5919
-
-
Garcia-Garcia, M.J.1
-
61
-
-
22944452718
-
Maternal fumonisin exposure and risk for neural tube defects: Mechanisms in an in vivo mouse model
-
Gelineau-van Waes J., et al. Maternal fumonisin exposure and risk for neural tube defects: Mechanisms in an in vivo mouse model. Birth Defects Res. A Clin. Mol. Teratol. 73 (2005) 487-497
-
(2005)
Birth Defects Res. A Clin. Mol. Teratol.
, vol.73
, pp. 487-497
-
-
Gelineau-van Waes, J.1
-
62
-
-
0030854129
-
Failure of neural tube closure in the loop-tail (Lp) mutant mouse: Analysis of the embryonic mechanism
-
Gerrelli D., and Copp A.J. Failure of neural tube closure in the loop-tail (Lp) mutant mouse: Analysis of the embryonic mechanism. Brain Res. Dev. Brain Res. 102 (1997) 217-224
-
(1997)
Brain Res. Dev. Brain Res.
, vol.102
, pp. 217-224
-
-
Gerrelli, D.1
Copp, A.J.2
-
63
-
-
0030866154
-
Altered neural cell fates and medulloblastoma in mouse patched mutants
-
Goodrich L.V., et al. Altered neural cell fates and medulloblastoma in mouse patched mutants. Science 277 (1997) 1109-1113
-
(1997)
Science
, vol.277
, pp. 1109-1113
-
-
Goodrich, L.V.1
-
64
-
-
0025875226
-
Pax-3, a novel murine DNA binding protein expressed during early neurogenesis
-
Goulding M.D., et al. Pax-3, a novel murine DNA binding protein expressed during early neurogenesis. EMBO J. 10 (1991) 1135-1147
-
(1991)
EMBO J.
, vol.10
, pp. 1135-1147
-
-
Goulding, M.D.1
-
65
-
-
0027324186
-
Analysis of the Pax-3 gene in the mouse mutant splotch
-
Goulding M., et al. Analysis of the Pax-3 gene in the mouse mutant splotch. Genomics 17 (1993) 355-363
-
(1993)
Genomics
, vol.17
, pp. 355-363
-
-
Goulding, M.1
-
66
-
-
0030027060
-
Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development
-
Greco T.L., et al. Analysis of the vestigial tail mutation demonstrates that Wnt-3a gene dosage regulates mouse axial development. Genes Dev. 10 (1996) 313-324
-
(1996)
Genes Dev.
, vol.10
, pp. 313-324
-
-
Greco, T.L.1
-
67
-
-
0031033593
-
Inositol prevents folate-resistant neural tube defects in the mouse
-
Greene N.D., and Copp A.J. Inositol prevents folate-resistant neural tube defects in the mouse. Nat. Med. 3 (1997) 60-66
-
(1997)
Nat. Med.
, vol.3
, pp. 60-66
-
-
Greene, N.D.1
Copp, A.J.2
-
68
-
-
17844390637
-
Mouse models of neural tube defects: Investigating preventive mechanisms
-
Greene N.D., and Copp A.J. Mouse models of neural tube defects: Investigating preventive mechanisms. Am. J. Med. Genet. C Semin. Med. Genet. 135C (2005) 31-41
-
(2005)
Am. J. Med. Genet. C Semin. Med. Genet.
, vol.135 C
, pp. 31-41
-
-
Greene, N.D.1
Copp, A.J.2
-
69
-
-
0031979611
-
Abnormalities of floor plate, notochord and somite differentiation in the loop-tail (Lp) mouse: A model of severe neural tube defects
-
Greene N.D., et al. Abnormalities of floor plate, notochord and somite differentiation in the loop-tail (Lp) mouse: A model of severe neural tube defects. Mech. Dev. 73 (1998) 59-72
-
(1998)
Mech. Dev.
, vol.73
, pp. 59-72
-
-
Greene, N.D.1
-
70
-
-
0346096641
-
Maternal myo-inositol, glucose, and zinc status is associated with the risk of offspring with spina bifida
-
Groenen P.M., et al. Maternal myo-inositol, glucose, and zinc status is associated with the risk of offspring with spina bifida. Am. J. Obstet. Gynecol. 189 (2003) 1713-1719
-
(2003)
Am. J. Obstet. Gynecol.
, vol.189
, pp. 1713-1719
-
-
Groenen, P.M.1
-
71
-
-
0002666312
-
Genetical studies on the skeleton of the mouse. VIII. Curly tail
-
Gruneberg H. Genetical studies on the skeleton of the mouse. VIII. Curly tail. J. Genet. 52 (1954) 52-67
-
(1954)
J. Genet.
, vol.52
, pp. 52-67
-
-
Gruneberg, H.1
-
72
-
-
0028089937
-
Open brain, a new mouse mutant with severe neural tube defects, shows altered gene expression patterns in the developing spinal cord
-
Gunther T., et al. Open brain, a new mouse mutant with severe neural tube defects, shows altered gene expression patterns in the developing spinal cord. Development 120 (1994) 3119-3130
-
(1994)
Development
, vol.120
, pp. 3119-3130
-
-
Gunther, T.1
-
73
-
-
35448973405
-
Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model
-
Gustavsson P., et al. Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model. Hum. Mol. Genet. 16 (2007) 2640-2646
-
(2007)
Hum. Mol. Genet.
, vol.16
, pp. 2640-2646
-
-
Gustavsson, P.1
-
74
-
-
0036931633
-
Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure
-
Hamblet N.S., et al. Dishevelled 2 is essential for cardiac outflow tract development, somite segmentation and neural tube closure. Development 129 (2002) 5827-5838
-
(2002)
Development
, vol.129
, pp. 5827-5838
-
-
Hamblet, N.S.1
-
75
-
-
33947172588
-
Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects
-
Harris M.J., and Juriloff D.M. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects. Birth Defects Res. A Clin. Mol. Teratol. 79 (2007) 187-210
-
(2007)
Birth Defects Res. A Clin. Mol. Teratol.
, vol.79
, pp. 187-210
-
-
Harris, M.J.1
Juriloff, D.M.2
-
76
-
-
40749144679
-
Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function
-
Haycraft C.J., et al. Gli2 and Gli3 localize to cilia and require the intraflagellar transport protein polaris for processing and function. PLoS Genet. 1 (2005) e53
-
(2005)
PLoS Genet.
, vol.1
-
-
Haycraft, C.J.1
-
77
-
-
0028978478
-
Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice
-
Helwig U., et al. Interaction between undulated and Patch leads to an extreme form of spina bifida in double-mutant mice. Nat. Genet. 11 (1995) 60-63
-
(1995)
Nat. Genet.
, vol.11
, pp. 60-63
-
-
Helwig, U.1
-
78
-
-
0028954840
-
A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome
-
Hol F.A., et al. A frameshift mutation in the gene for PAX3 in a girl with spina bifida and mild signs of Waardenburg syndrome. J. Med. Genet. 32 (1995) 52-56
-
(1995)
J. Med. Genet.
, vol.32
, pp. 52-56
-
-
Hol, F.A.1
-
79
-
-
0029784135
-
PAX genes and human neural tube defects: An amino acid substitution in PAX1 in a patient with spina bifida
-
Hol F.A., et al. PAX genes and human neural tube defects: An amino acid substitution in PAX1 in a patient with spina bifida. J. Med. Genet. 33 (1996) 655-660
-
(1996)
J. Med. Genet.
, vol.33
, pp. 655-660
-
-
Hol, F.A.1
-
80
-
-
0027439075
-
Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I)
-
Hoth C.F., et al. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg syndrome (WS-III) as well as Waardenburg syndrome type I (WS-I). Am. J. Hum. Genet. 52 (1993) 455-462
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 455-462
-
-
Hoth, C.F.1
-
81
-
-
33845397717
-
Hippi is essential for node cilia assembly and Sonic hedgehog signaling
-
Houde C., et al. Hippi is essential for node cilia assembly and Sonic hedgehog signaling. Dev. Biol. 300 (2006) 523-533
-
(2006)
Dev. Biol.
, vol.300
, pp. 523-533
-
-
Houde, C.1
-
82
-
-
23844485210
-
Cilia and Hedgehog responsiveness in the mouse
-
Huangfu D., and Anderson K.V. Cilia and Hedgehog responsiveness in the mouse. Proc. Natl Acad. Sci. USA 102 (2005) 11325-11330
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 11325-11330
-
-
Huangfu, D.1
Anderson, K.V.2
-
83
-
-
0242581681
-
Hedgehog signalling in the mouse requires intraflagellar transport proteins
-
Huangfu D., et al. Hedgehog signalling in the mouse requires intraflagellar transport proteins. Nature 426 (2003) 83-87
-
(2003)
Nature
, vol.426
, pp. 83-87
-
-
Huangfu, D.1
-
84
-
-
0027478216
-
A mouse model of greig cephalopolysyndactyly syndrome: The extra-toesJ mutation contains an intragenic deletion of the Gli3 gene
-
Hui C.C., and Joyner A.L. A mouse model of greig cephalopolysyndactyly syndrome: The extra-toesJ mutation contains an intragenic deletion of the Gli3 gene. Nat. Genet. 3 (1993) 241-246
-
(1993)
Nat. Genet.
, vol.3
, pp. 241-246
-
-
Hui, C.C.1
Joyner, A.L.2
-
85
-
-
0029036701
-
A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase
-
Huibregtse J.M., et al. A family of proteins structurally and functionally related to the E6-AP ubiquitin-protein ligase. Proc. Natl Acad. Sci. USA 92 (1995) 5249
-
(1995)
Proc. Natl Acad. Sci. USA
, vol.92
, pp. 5249
-
-
Huibregtse, J.M.1
-
86
-
-
20944448235
-
Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs
-
Jadeja S., et al. Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Nat. Genet. 37 (2005) 520-525
-
(2005)
Nat. Genet.
, vol.37
, pp. 520-525
-
-
Jadeja, S.1
-
87
-
-
0032564483
-
Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins
-
Joosten P.H., et al. Altered regulation of platelet-derived growth factor receptor-alpha gene-transcription in vitro by spina bifida-associated mutant Pax1 proteins. Proc. Natl Acad. Sci. USA 95 (1998) 14459-14463
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 14459-14463
-
-
Joosten, P.H.1
-
88
-
-
0035136746
-
Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects
-
Joosten P.H., et al. Promoter haplotype combinations of the platelet-derived growth factor alpha-receptor gene predispose to human neural tube defects. Nat. Genet. 27 (2001) 215-217
-
(2001)
Nat. Genet.
, vol.27
, pp. 215-217
-
-
Joosten, P.H.1
-
89
-
-
28244500565
-
Pax1/E2a double-mutant mice develop non-lethal neural tube defects that resemble human malformations
-
Joosten P.H., et al. Pax1/E2a double-mutant mice develop non-lethal neural tube defects that resemble human malformations. Transgenic Res. 14 (2005) 983-987
-
(2005)
Transgenic Res.
, vol.14
, pp. 983-987
-
-
Joosten, P.H.1
-
90
-
-
13844292417
-
Antenatal presentation of Bardet-Biedl syndrome may mimic Meckel syndrome
-
Karmous-Benailly H., et al. Antenatal presentation of Bardet-Biedl syndrome may mimic Meckel syndrome. Am. J. Hum. Genet. 76 (2005) 493-504
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 493-504
-
-
Karmous-Benailly, H.1
-
91
-
-
0032560518
-
A phenotype-based screen for embryonic lethal mutations in the mouse
-
Kasarskis A., et al. A phenotype-based screen for embryonic lethal mutations in the mouse. Proc. Natl Acad. Sci. USA 95 (1998) 7485-7490
-
(1998)
Proc. Natl Acad. Sci. USA
, vol.95
, pp. 7485-7490
-
-
Kasarskis, A.1
-
92
-
-
0031976447
-
Dietary myo-inositol therapy in hyperglycemia-induced embryopathy
-
Khandelwal M., et al. Dietary myo-inositol therapy in hyperglycemia-induced embryopathy. Teratology 57 (1998) 79-84
-
(1998)
Teratology
, vol.57
, pp. 79-84
-
-
Khandelwal, M.1
-
93
-
-
0034931874
-
Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail
-
Kibar Z., et al. Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail. Nat. Genet. 28 (2001) 251-255
-
(2001)
Nat. Genet.
, vol.28
, pp. 251-255
-
-
Kibar, Z.1
-
94
-
-
34247570440
-
Toward understanding the genetic basis of neural tube defects
-
Kibar Z., et al. Toward understanding the genetic basis of neural tube defects. Clin. Genet. 71 (2007) 295-310
-
(2007)
Clin. Genet.
, vol.71
, pp. 295-310
-
-
Kibar, Z.1
-
95
-
-
34047261773
-
Mutations in VANGL1 associated with neural-tube defects
-
Kibar Z., et al. Mutations in VANGL1 associated with neural-tube defects. N. Engl. J. Med. 356 (2007) 1432-1437
-
(2007)
N. Engl. J. Med.
, vol.356
, pp. 1432-1437
-
-
Kibar, Z.1
-
96
-
-
0034769937
-
Srg3, a mouse homolog of yeast SWI3, is essential for early embryogenesis and involved in brain development
-
Kim J.K., et al. Srg3, a mouse homolog of yeast SWI3, is essential for early embryogenesis and involved in brain development. Mol. Cell. Biol. 21 (2001) 7787-7795
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 7787-7795
-
-
Kim, J.K.1
-
97
-
-
0034058117
-
Expression of the sonic hedgehog gene in human embryos with neural tube defects
-
Kirillova I., et al. Expression of the sonic hedgehog gene in human embryos with neural tube defects. Teratology 61 (2000) 347-354
-
(2000)
Teratology
, vol.61
, pp. 347-354
-
-
Kirillova, I.1
-
98
-
-
0027145847
-
Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects
-
Kirke P.N., et al. Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects. Q. J. Med. 86 (1993) 703-708
-
(1993)
Q. J. Med.
, vol.86
, pp. 703-708
-
-
Kirke, P.N.1
-
99
-
-
0036007120
-
An allelic series at the PDGFalphaR locus indicates unequal contributions of distinct signaling pathways during development
-
Klinghoffer R.A., et al. An allelic series at the PDGFalphaR locus indicates unequal contributions of distinct signaling pathways during development. Dev. Cell 2 (2002) 103-113
-
(2002)
Dev. Cell
, vol.2
, pp. 103-113
-
-
Klinghoffer, R.A.1
-
100
-
-
33847052754
-
Prenatal diagnosis and genetic counseling in a case of spina bifida in a family with Waardenburg syndrome type I
-
Kujat A., et al. Prenatal diagnosis and genetic counseling in a case of spina bifida in a family with Waardenburg syndrome type I. Fetal Diagn. Ther. 22 (2007) 155-158
-
(2007)
Fetal Diagn. Ther.
, vol.22
, pp. 155-158
-
-
Kujat, A.1
-
101
-
-
31744435454
-
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome
-
Kyttala M., et al. MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome. Nat. Genet. 38 (2006) 155-157
-
(2006)
Nat. Genet.
, vol.38
, pp. 155-157
-
-
Kyttala, M.1
-
102
-
-
0033178548
-
Neurofibromin deficiency in mice causes exencephaly and is a modifier for Splotch neural tube defects
-
Lakkis M.M., et al. Neurofibromin deficiency in mice causes exencephaly and is a modifier for Splotch neural tube defects. Dev. Biol. 212 (1999) 80-92
-
(1999)
Dev. Biol.
, vol.212
, pp. 80-92
-
-
Lakkis, M.M.1
-
103
-
-
41349103272
-
Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome
-
Leitch C.C., et al. Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome. Nat. Genet. 40 (2008) 443-448
-
(2008)
Nat. Genet.
, vol.40
, pp. 443-448
-
-
Leitch, C.C.1
-
104
-
-
0028856888
-
A curly-tail modifier locus, mct1, on mouse chromosome 17
-
Letts V.A., et al. A curly-tail modifier locus, mct1, on mouse chromosome 17. Genomics 29 (1995) 719-724
-
(1995)
Genomics
, vol.29
, pp. 719-724
-
-
Letts, V.A.1
-
105
-
-
33846822914
-
Expression of the gene encoding the high-Km glucose transporter 2 by the early postimplantation mouse embryo is essential for neural tube defects associated with diabetic embryopathy
-
Li R., et al. Expression of the gene encoding the high-Km glucose transporter 2 by the early postimplantation mouse embryo is essential for neural tube defects associated with diabetic embryopathy. Diabetologia 50 (2007) 682-689
-
(2007)
Diabetologia
, vol.50
, pp. 682-689
-
-
Li, R.1
-
106
-
-
0005015546
-
The occurrence of two heritable types of abnormality among descendants of X-rayed mice
-
Little C., and Bagg H. The occurrence of two heritable types of abnormality among descendants of X-rayed mice. Am. J. Roentgenol. 10 (1923) 975-989
-
(1923)
Am. J. Roentgenol.
, vol.10
, pp. 975-989
-
-
Little, C.1
Bagg, H.2
-
107
-
-
23144466931
-
Mouse intraflagellar transport proteins regulate both the activator and repressor functions of Gli transcription factors
-
Liu A., et al. Mouse intraflagellar transport proteins regulate both the activator and repressor functions of Gli transcription factors. Development 132 (2005) 3103-3111
-
(2005)
Development
, vol.132
, pp. 3103-3111
-
-
Liu, A.1
-
108
-
-
17844386819
-
Current perspectives on the causes of neural tube defects resulting from diabetic pregnancy
-
Loeken M.R. Current perspectives on the causes of neural tube defects resulting from diabetic pregnancy. Am. J. Med. Genet. C Semin. Med. Genet. 135 (2005) 77-87
-
(2005)
Am. J. Med. Genet. C Semin. Med. Genet.
, vol.135
, pp. 77-87
-
-
Loeken, M.R.1
-
109
-
-
3042845655
-
PTK7/CCK-4 is a novel regulator of planar cell polarity in vertebrates
-
Lu X., et al. PTK7/CCK-4 is a novel regulator of planar cell polarity in vertebrates. Nature 430 (2004) 93-98
-
(2004)
Nature
, vol.430
, pp. 93-98
-
-
Lu, X.1
-
111
-
-
11144357212
-
Fumonisins disrupt sphingolipid metabolism, folate transport, and neural tube development in embryo culture and in vivo: A potential risk factor for human neural tube defects among populations consuming fumonisin-contaminated maize
-
Marasas W.F., et al. Fumonisins disrupt sphingolipid metabolism, folate transport, and neural tube development in embryo culture and in vivo: A potential risk factor for human neural tube defects among populations consuming fumonisin-contaminated maize. J. Nutr. 134 (2004) 711-716
-
(2004)
J. Nutr.
, vol.134
, pp. 711-716
-
-
Marasas, W.F.1
-
112
-
-
27744484694
-
Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli
-
May S.R., et al. Loss of the retrograde motor for IFT disrupts localization of Smo to cilia and prevents the expression of both activator and repressor functions of Gli. Dev. Biol. 287 (2005) 378-389
-
(2005)
Dev. Biol.
, vol.287
, pp. 378-389
-
-
May, S.R.1
-
113
-
-
0037872680
-
Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein
-
McGregor L., et al. Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein. Nat. Genet. 34 (2003) 203-208
-
(2003)
Nat. Genet.
, vol.34
, pp. 203-208
-
-
McGregor, L.1
-
114
-
-
0031020221
-
Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development
-
Mo R., et al. Specific and redundant functions of Gli2 and Gli3 zinc finger genes in skeletal patterning and development. Development 124 (1997) 113-123
-
(1997)
Development
, vol.124
, pp. 113-123
-
-
Mo, R.1
-
115
-
-
0027268525
-
Waardenburg syndrome and meningomyelocele
-
Moline M.L., and Sandlin C. Waardenburg syndrome and meningomyelocele. Am. J. Med. Genet. 47 (1993) 126
-
(1993)
Am. J. Med. Genet.
, vol.47
, pp. 126
-
-
Moline, M.L.1
Sandlin, C.2
-
116
-
-
33646941288
-
Asymmetric localization of Vangl2 and Fz3 indicate novel mechanisms for planar cell polarity in mammals
-
Montcouquiol M., et al. Asymmetric localization of Vangl2 and Fz3 indicate novel mechanisms for planar cell polarity in mammals. J. Neurosci. 26 (2006) 5265-5275
-
(2006)
J. Neurosci.
, vol.26
, pp. 5265-5275
-
-
Montcouquiol, M.1
-
117
-
-
0026663734
-
A PDGF receptor mutation in the mouse (Patch) perturbs the development of a non-neuronal subset of neural crest-derived cells
-
Morrison-Graham K., et al. A PDGF receptor mutation in the mouse (Patch) perturbs the development of a non-neuronal subset of neural crest-derived cells. Development 115 (1992) 133-142
-
(1992)
Development
, vol.115
, pp. 133-142
-
-
Morrison-Graham, K.1
-
118
-
-
0035888642
-
Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification
-
Murdoch J.N., et al. Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification. Hum. Mol. Genet. 10 (2001) 2593-2601
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2593-2601
-
-
Murdoch, J.N.1
-
119
-
-
0037439541
-
Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse
-
Murdoch J.N., et al. Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse. Hum. Mol. Genet. 12 (2003) 87-98
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 87-98
-
-
Murdoch, J.N.1
-
120
-
-
0028244488
-
Multifactorial inheritance of neural tube defects: Localization of the major gene and recognition of modifiers in ct mutant mice
-
Neumann P.E., et al. Multifactorial inheritance of neural tube defects: Localization of the major gene and recognition of modifiers in ct mutant mice. Nat. Genet. 6 (1994) 357-362
-
(1994)
Nat. Genet.
, vol.6
, pp. 357-362
-
-
Neumann, P.E.1
-
121
-
-
0032477782
-
Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: Possible digenic inheritance of a neural tube defect
-
Nye J.S., et al. Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: Possible digenic inheritance of a neural tube defect. Am. J. Med. Genet. 75 (1998) 401-408
-
(1998)
Am. J. Med. Genet.
, vol.75
, pp. 401-408
-
-
Nye, J.S.1
-
122
-
-
0026695298
-
Developmental expression of the alpha receptor for platelet-derived growth factor, which is deleted in the embryonic lethal Patch mutation
-
Orr-Urtreger A., et al. Developmental expression of the alpha receptor for platelet-derived growth factor, which is deleted in the embryonic lethal Patch mutation. Development 115 (1992) 289-303
-
(1992)
Development
, vol.115
, pp. 289-303
-
-
Orr-Urtreger, A.1
-
123
-
-
0036723777
-
Polymorphic susceptibility to the molecular causes of neural tube defects during diabetic embryopathy
-
Pani L., et al. Polymorphic susceptibility to the molecular causes of neural tube defects during diabetic embryopathy. Diabetes 51 (2002) 2871-2874
-
(2002)
Diabetes
, vol.51
, pp. 2871-2874
-
-
Pani, L.1
-
124
-
-
0037087629
-
Rescue of neural tube defects in Pax-3-deficient embryos by p53 loss of function: Implications for Pax-3-dependent development and tumorigenesis
-
Pani L., et al. Rescue of neural tube defects in Pax-3-deficient embryos by p53 loss of function: Implications for Pax-3-dependent development and tumorigenesis. Genes Dev. 16 (2002) 676-680
-
(2002)
Genes Dev.
, vol.16
, pp. 676-680
-
-
Pani, L.1
-
126
-
-
0013901399
-
Syndrome of caudal regression in infants of diabetic mothers: Observations of further cases
-
Passarge E., and Lenz W. Syndrome of caudal regression in infants of diabetic mothers: Observations of further cases. Pediatrics 37 (1966) 672-675
-
(1966)
Pediatrics
, vol.37
, pp. 672-675
-
-
Passarge, E.1
Lenz, W.2
-
127
-
-
0030899177
-
Spina bifida occulta in homozygous Patch mouse embryos
-
Payne J., et al. Spina bifida occulta in homozygous Patch mouse embryos. Dev. Dyn. 209 (1997) 105-116
-
(1997)
Dev. Dyn.
, vol.209
, pp. 105-116
-
-
Payne, J.1
-
128
-
-
0036220971
-
The mouse Fused toes (Ft) mutation is the result of a 1.6-Mb deletion including the entire Iroquois B gene cluster
-
Peters T., et al. The mouse Fused toes (Ft) mutation is the result of a 1.6-Mb deletion including the entire Iroquois B gene cluster. Mamm. Genome 13 (2002) 186-188
-
(2002)
Mamm. Genome
, vol.13
, pp. 186-188
-
-
Peters, T.1
-
129
-
-
0030994305
-
Neural tube defects in embryos of diabetic mice: Role of the Pax-3 gene and apoptosis
-
Phelan S.A., et al. Neural tube defects in embryos of diabetic mice: Role of the Pax-3 gene and apoptosis. Diabetes 46 (1997) 1189-1197
-
(1997)
Diabetes
, vol.46
, pp. 1189-1197
-
-
Phelan, S.A.1
-
131
-
-
39749148788
-
Disruption of PDGFRalpha-initiated PI3K activation and migration of somite derivatives leads to spina bifida
-
Pickett E.A., et al. Disruption of PDGFRalpha-initiated PI3K activation and migration of somite derivatives leads to spina bifida. Development 135 (2008) 589-598
-
(2008)
Development
, vol.135
, pp. 589-598
-
-
Pickett, E.A.1
-
132
-
-
34249664330
-
Wnt5a functions in planar cell polarity regulation in mice
-
Qian D., et al. Wnt5a functions in planar cell polarity regulation in mice. Dev. Biol. 306 (2007) 121-133
-
(2007)
Dev. Biol.
, vol.306
, pp. 121-133
-
-
Qian, D.1
-
133
-
-
34547110771
-
Patched1 regulates hedgehog signaling at the primary cilium
-
Rohatgi R., et al. Patched1 regulates hedgehog signaling at the primary cilium. Science 317 (2007) 372-376
-
(2007)
Science
, vol.317
, pp. 372-376
-
-
Rohatgi, R.1
-
134
-
-
27144460671
-
Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates
-
Ross A.J., et al. Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates. Nat. Genet. 37 (2005) 1135-1140
-
(2005)
Nat. Genet.
, vol.37
, pp. 1135-1140
-
-
Ross, A.J.1
-
135
-
-
0036393805
-
Prevention of fumonisin B1-induced neural tube defects by folic acid
-
Sadler T.W., et al. Prevention of fumonisin B1-induced neural tube defects by folic acid. Teratology 66 (2002) 169-176
-
(2002)
Teratology
, vol.66
, pp. 169-176
-
-
Sadler, T.W.1
-
136
-
-
33646164168
-
Intraflagellar transport and cilium-based signaling
-
Scholey J.M., and Anderson K.V. Intraflagellar transport and cilium-based signaling. Cell 125 (2006) 439-442
-
(2006)
Cell
, vol.125
, pp. 439-442
-
-
Scholey, J.M.1
Anderson, K.V.2
-
137
-
-
0020576287
-
The cause of neural tube defects: Some experiments and a hypothesis
-
Seller M.J. The cause of neural tube defects: Some experiments and a hypothesis. J. Med. Genet. 20 (1983) 164-168
-
(1983)
J. Med. Genet.
, vol.20
, pp. 164-168
-
-
Seller, M.J.1
-
138
-
-
0019833128
-
The curly-tail mouse: An experimental model for human neural tube defects
-
Seller M.J., and Adinolfi M. The curly-tail mouse: An experimental model for human neural tube defects. Life Sci. 29 (1981) 1607-1615
-
(1981)
Life Sci.
, vol.29
, pp. 1607-1615
-
-
Seller, M.J.1
Adinolfi, M.2
-
139
-
-
0020957147
-
Effect of hydroxyurea on neural tube defects in the curly-tail mouse
-
Seller M.J., and Perkins K.J. Effect of hydroxyurea on neural tube defects in the curly-tail mouse. J. Craniofac. Genet. Dev. Biol. 3 (1983) 11-17
-
(1983)
J. Craniofac. Genet. Dev. Biol.
, vol.3
, pp. 11-17
-
-
Seller, M.J.1
Perkins, K.J.2
-
140
-
-
0022538284
-
Effect of mitomycin C on the neural tube defects of the curly-tail mouse
-
Seller M.J., and Perkins K.J. Effect of mitomycin C on the neural tube defects of the curly-tail mouse. Teratology 33 (1986) 305-309
-
(1986)
Teratology
, vol.33
, pp. 305-309
-
-
Seller, M.J.1
Perkins, K.J.2
-
141
-
-
3242704306
-
Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects
-
Shim S.H., et al. Molecular cytogenetic characterization of multiple intrachromosomal rearrangements of chromosome 2q in a patient with Waardenburg's syndrome and other congenital defects. Clin. Genet. 66 (2004) 46-52
-
(2004)
Clin. Genet.
, vol.66
, pp. 46-52
-
-
Shim, S.H.1
-
142
-
-
0032780716
-
Retinoic acid induces down-regulation of Wnt-3a, apoptosis and diversion of tail bud cells to a neural fate in the mouse embryo
-
Shum A.S., et al. Retinoic acid induces down-regulation of Wnt-3a, apoptosis and diversion of tail bud cells to a neural fate in the mouse embryo. Mech. Dev. 84 (1999) 17-30
-
(1999)
Mech. Dev.
, vol.84
, pp. 17-30
-
-
Shum, A.S.1
-
143
-
-
0002159175
-
Axial elongation in the mouse and its retardation in homozygous looptail mice
-
Smith L.J., and Stein K.F. Axial elongation in the mouse and its retardation in homozygous looptail mice. J. Embryol. Exp. Morphol. 10 (1962) 73-87
-
(1962)
J. Embryol. Exp. Morphol.
, vol.10
, pp. 73-87
-
-
Smith, L.J.1
Stein, K.F.2
-
144
-
-
0025829301
-
Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5
-
Smith E.A., et al. Mouse platelet-derived growth factor receptor alpha gene is deleted in W19H and patch mutations on chromosome 5. Proc. Natl Acad. Sci. USA 88 (1991) 4811-4815
-
(1991)
Proc. Natl Acad. Sci. USA
, vol.88
, pp. 4811-4815
-
-
Smith, E.A.1
-
145
-
-
31744441248
-
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat
-
Smith U.M., et al. The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat. Nat. Genet. 38 (2006) 191-196
-
(2006)
Nat. Genet.
, vol.38
, pp. 191-196
-
-
Smith, U.M.1
-
146
-
-
0017097661
-
Vitamin deficiencies and neural tube defects
-
Smithells R.W., et al. Vitamin deficiencies and neural tube defects. Arch. Dis. Child. 51 (1976) 944-950
-
(1976)
Arch. Dis. Child.
, vol.51
, pp. 944-950
-
-
Smithells, R.W.1
-
147
-
-
0018881168
-
Possible prevention of neural-tube defects by periconceptional vitamin supplementation
-
Smithells R.W., et al. Possible prevention of neural-tube defects by periconceptional vitamin supplementation. Lancet 1 (1980) 339-340
-
(1980)
Lancet
, vol.1
, pp. 339-340
-
-
Smithells, R.W.1
-
148
-
-
27744516069
-
The genetics of Fraser syndrome and the blebs mouse mutants
-
Smyth I., and Scambler P. The genetics of Fraser syndrome and the blebs mouse mutants. Hum. Mol. Genet. 14 Spec No. 2 (2005) R269-R274
-
(2005)
Hum. Mol. Genet.
, vol.14
, Issue.Spec 2
-
-
Smyth, I.1
Scambler, P.2
-
149
-
-
4544312319
-
The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis
-
Smyth I., et al. The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis. Proc. Natl Acad. Sci. USA 101 (2004) 13560-13565
-
(2004)
Proc. Natl Acad. Sci. USA
, vol.101
, pp. 13560-13565
-
-
Smyth, I.1
-
150
-
-
0344157814
-
Paradox segmentation along inter- and intrasomitic borderlines is followed by dysmorphology of the axial skeleton in the open brain (opb) mouse mutant
-
Sporle R., and Schughart K. Paradox segmentation along inter- and intrasomitic borderlines is followed by dysmorphology of the axial skeleton in the open brain (opb) mouse mutant. Dev. Genet. 22 (1998) 359-373
-
(1998)
Dev. Genet.
, vol.22
, pp. 359-373
-
-
Sporle, R.1
Schughart, K.2
-
151
-
-
0030025659
-
Severe defects in the formation of epaxial musculature in open brain (opb) mutant mouse embryos
-
Sporle R., et al. Severe defects in the formation of epaxial musculature in open brain (opb) mutant mouse embryos. Development 122 (1996) 79-86
-
(1996)
Development
, vol.122
, pp. 79-86
-
-
Sporle, R.1
-
152
-
-
0026020611
-
Platelet-derived growth factor receptor alpha-subunit gene (Pdgfra) is deleted in the mouse patch (Ph) mutation
-
Stephenson D.A., et al. Platelet-derived growth factor receptor alpha-subunit gene (Pdgfra) is deleted in the mouse patch (Ph) mutation. Proc. Natl Acad. Sci. USA 88 (1991) 6-10
-
(1991)
Proc. Natl Acad. Sci. USA
, vol.88
, pp. 6-10
-
-
Stephenson, D.A.1
-
153
-
-
0030610575
-
Fumonisin B1-induced sphingolipid depletion inhibits vitamin uptake via the glycosylphosphatidylinositol-anchored folate receptor
-
Stevens V.L., and Tang J. Fumonisin B1-induced sphingolipid depletion inhibits vitamin uptake via the glycosylphosphatidylinositol-anchored folate receptor. J. Biol. Chem. 272 (1997) 18020-18025
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 18020-18025
-
-
Stevens, V.L.1
Tang, J.2
-
154
-
-
0141721305
-
Tethering of the spinal cord in mouse fetuses and neonates with spina bifida
-
Stiefel D., et al. Tethering of the spinal cord in mouse fetuses and neonates with spina bifida. J. Neurosurg. 99 (2003) 206-213
-
(2003)
J. Neurosurg.
, vol.99
, pp. 206-213
-
-
Stiefel, D.1
-
155
-
-
0001511418
-
Hereditary loop-tail in the house mouse accompanied by imperforate vagina and craniorachischisis when homozygous
-
Strong L., and Hollander W. Hereditary loop-tail in the house mouse accompanied by imperforate vagina and craniorachischisis when homozygous. J. Hered. 40 (1949) 329-334
-
(1949)
J. Hered.
, vol.40
, pp. 329-334
-
-
Strong, L.1
Hollander, W.2
-
156
-
-
0033847998
-
Developmental eye and neural tube defects in the eye blebs mouse
-
Swiergiel J.J., et al. Developmental eye and neural tube defects in the eye blebs mouse. Dev. Dyn. 219 (2000) 21-27
-
(2000)
Dev. Dyn.
, vol.219
, pp. 21-27
-
-
Swiergiel, J.J.1
-
157
-
-
0028157392
-
Wnt-3a regulates somite and tailbud formation in the mouse embryo
-
Takada S., et al. Wnt-3a regulates somite and tailbud formation in the mouse embryo. Genes Dev. 8 (1994) 174-189
-
(1994)
Genes Dev.
, vol.8
, pp. 174-189
-
-
Takada, S.1
-
158
-
-
0842310833
-
A direct functional link between the multi-PDZ domain protein GRIP1 and the Fraser syndrome protein Fras1
-
Takamiya K., et al. A direct functional link between the multi-PDZ domain protein GRIP1 and the Fraser syndrome protein Fras1. Nat. Genet. 36 (2004) 172-177
-
(2004)
Nat. Genet.
, vol.36
, pp. 172-177
-
-
Takamiya, K.1
-
159
-
-
0032513114
-
The role of E6AP in the regulation of p53 protein levels in human papillomavirus (HPV)-positive and HPV-negative cells
-
Talis A.L., et al. The role of E6AP in the regulation of p53 protein levels in human papillomavirus (HPV)-positive and HPV-negative cells. J. Biol. Chem. 273 (1998) 6439-6445
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 6439-6445
-
-
Talis, A.L.1
-
160
-
-
23844445146
-
Tissue morphogenesis and vascular stability require the Frem2 protein, product of the mouse myelencephalic blebs gene
-
Timmer J.R., et al. Tissue morphogenesis and vascular stability require the Frem2 protein, product of the mouse myelencephalic blebs gene. Proc. Natl Acad. Sci. USA 102 (2005) 11746-11750
-
(2005)
Proc. Natl Acad. Sci. USA
, vol.102
, pp. 11746-11750
-
-
Timmer, J.R.1
-
161
-
-
0348107340
-
Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3
-
Ting S.B., et al. Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3. Nat. Med. 9 (2003) 1513-1519
-
(2003)
Nat. Med.
, vol.9
, pp. 1513-1519
-
-
Ting, S.B.1
-
162
-
-
20244389223
-
A homolog of Drosophila grainy head is essential for epidermal integrity in mice
-
Ting S.B., et al. A homolog of Drosophila grainy head is essential for epidermal integrity in mice. Science 308 (2005) 411-413
-
(2005)
Science
, vol.308
, pp. 411-413
-
-
Ting, S.B.1
-
163
-
-
10644297971
-
Independent mutations in mouse Vangl2 that cause neural tube defects in looptail mice impair interaction with members of the Dishevelled family
-
Torban E., et al. Independent mutations in mouse Vangl2 that cause neural tube defects in looptail mice impair interaction with members of the Dishevelled family. J. Biol. Chem. 279 (2004) 52703-52713
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 52703-52713
-
-
Torban, E.1
-
164
-
-
42149191189
-
Genetic interaction between members of the Vangl family causes neural tube defects in mice
-
Torban E., et al. Genetic interaction between members of the Vangl family causes neural tube defects in mice. Proc. Natl Acad. Sci. USA 105 (2008) 3449-3454
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 3449-3454
-
-
Torban, E.1
-
165
-
-
36849036401
-
Morphogens and the control of cell proliferation and patterning in the spinal cord
-
Ulloa F., and Briscoe J. Morphogens and the control of cell proliferation and patterning in the spinal cord. Cell Cycle 6 (2007) 2640-2649
-
(2007)
Cell Cycle
, vol.6
, pp. 2640-2649
-
-
Ulloa, F.1
Briscoe, J.2
-
166
-
-
0028025622
-
Programmed cell death is affected in the novel mouse mutant Fused toes (Ft)
-
van der Hoeven F., et al. Programmed cell death is affected in the novel mouse mutant Fused toes (Ft). Development 120 (1994) 2601-2607
-
(1994)
Development
, vol.120
, pp. 2601-2607
-
-
van der Hoeven, F.1
-
167
-
-
0030864413
-
Altered folate and vitamin B12 metabolism in families with spina bifida offspring
-
van der Put N.M., et al. Altered folate and vitamin B12 metabolism in families with spina bifida offspring. Q. J. Med. 90 (1997) 505-510
-
(1997)
Q. J. Med.
, vol.90
, pp. 505-510
-
-
van der Put, N.M.1
-
168
-
-
0035041246
-
Curly tail: A 50-year history of the mouse spina bifida model
-
van Straaten H.W., and Copp A.J. Curly tail: A 50-year history of the mouse spina bifida model. Anat. Embryol. (Berl.) 203 (2001) 225-237
-
(2001)
Anat. Embryol. (Berl.)
, vol.203
, pp. 225-237
-
-
van Straaten, H.W.1
Copp, A.J.2
-
169
-
-
0028847102
-
Dietary methionine does not reduce penetrance in curly tail mice but causes a phenotype-specific decrease in embryonic growth
-
van Straaten H.W., et al. Dietary methionine does not reduce penetrance in curly tail mice but causes a phenotype-specific decrease in embryonic growth. J. Nutr. 125 (1995) 2733-2740
-
(1995)
J. Nutr.
, vol.125
, pp. 2733-2740
-
-
van Straaten, H.W.1
-
171
-
-
34547800833
-
Ftm is a novel basal body protein of cilia involved in Shh signalling
-
Vierkotten J., et al. Ftm is a novel basal body protein of cilia involved in Shh signalling. Development 134 (2007) 2569-2577
-
(2007)
Development
, vol.134
, pp. 2569-2577
-
-
Vierkotten, J.1
-
172
-
-
0027338132
-
The splotch-delayed (Spd) mouse mutant carries a point mutation within the paired box of the Pax-3 gene
-
Vogan K.J., et al. The splotch-delayed (Spd) mouse mutant carries a point mutation within the paired box of the Pax-3 gene. Genomics 17 (1993) 364-369
-
(1993)
Genomics
, vol.17
, pp. 364-369
-
-
Vogan, K.J.1
-
173
-
-
0038617716
-
Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice
-
Vrontou S., et al. Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice. Nat. Genet. 34 (2003) 209-214
-
(2003)
Nat. Genet.
, vol.34
, pp. 209-214
-
-
Vrontou, S.1
-
174
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group
-
Wald N., et al. Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group. Lancet 338 (1991) 131-137
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
Wald, N.1
-
175
-
-
33749018196
-
Planar cell polarity, ciliogenesis and neural tube defects
-
Wallingford J.B. Planar cell polarity, ciliogenesis and neural tube defects. Hum. Mol. Genet. 15 Spec No. 2 (2006) R227-R234
-
(2006)
Hum. Mol. Genet.
, vol.15
, Issue.Spec 2
-
-
Wallingford, J.B.1
-
176
-
-
0034915909
-
Xenopus Dishevelled signaling regulates both neural and mesodermal convergent extension: Parallel forces elongating the body axis
-
Wallingford J.B., and Harland R.M. Xenopus Dishevelled signaling regulates both neural and mesodermal convergent extension: Parallel forces elongating the body axis. Development 128 (2001) 2581-2592
-
(2001)
Development
, vol.128
, pp. 2581-2592
-
-
Wallingford, J.B.1
Harland, R.M.2
-
177
-
-
0036922915
-
Neural tube closure requires Dishevelled-dependent convergent extension of the midline
-
Wallingford J.B., and Harland R.M. Neural tube closure requires Dishevelled-dependent convergent extension of the midline. Development 129 (2002) 5815-5825
-
(2002)
Development
, vol.129
, pp. 5815-5825
-
-
Wallingford, J.B.1
Harland, R.M.2
-
178
-
-
0034604076
-
Dishevelled controls cell polarity during Xenopus gastrulation
-
Wallingford J.B., et al. Dishevelled controls cell polarity during Xenopus gastrulation. Nature 405 (2000) 81-85
-
(2000)
Nature
, vol.405
, pp. 81-85
-
-
Wallingford, J.B.1
-
179
-
-
33947327064
-
Tissue/planar cell polarity in vertebrates: New insights and new questions
-
Wang Y., and Nathans J. Tissue/planar cell polarity in vertebrates: New insights and new questions. Development 134 (2007) 647-658
-
(2007)
Development
, vol.134
, pp. 647-658
-
-
Wang, Y.1
Nathans, J.2
-
180
-
-
33744547152
-
Dishevelled genes mediate a conserved mammalian PCP pathway to regulate convergent extension during neurulation
-
Wang J., et al. Dishevelled genes mediate a conserved mammalian PCP pathway to regulate convergent extension during neurulation. Development 133 (2006) 1767-1778
-
(2006)
Development
, vol.133
, pp. 1767-1778
-
-
Wang, J.1
-
181
-
-
33645637038
-
The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells
-
Wang Y., et al. The role of Frizzled3 and Frizzled6 in neural tube closure and in the planar polarity of inner-ear sensory hair cells. J. Neurosci. 26 (2006) 2147-2156
-
(2006)
J. Neurosci.
, vol.26
, pp. 2147-2156
-
-
Wang, Y.1
-
182
-
-
0028307629
-
Analysis of neurulation in a mouse model for neural dysraphism
-
Wilson D.B., and Wyatt D.P. Analysis of neurulation in a mouse model for neural dysraphism. Exp. Neurol. 127 (1994) 154-158
-
(1994)
Exp. Neurol.
, vol.127
, pp. 154-158
-
-
Wilson, D.B.1
Wyatt, D.P.2
-
183
-
-
28144456841
-
Mode of action: Inhibition of histone deacetylase, altering WNT-dependent gene expression, and regulation of beta-catenin-Developmental effects of valproic acid
-
Wiltse J. Mode of action: Inhibition of histone deacetylase, altering WNT-dependent gene expression, and regulation of beta-catenin-Developmental effects of valproic acid. Crit. Rev. Toxicol. 35 (2005) 727-738
-
(2005)
Crit. Rev. Toxicol.
, vol.35
, pp. 727-738
-
-
Wiltse, J.1
-
184
-
-
0042819670
-
Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome
-
Wollnik B., et al. Homozygous and heterozygous inheritance of PAX3 mutations causes different types of Waardenburg syndrome. Am. J. Med. Genet. A 122 (2003) 42-45
-
(2003)
Am. J. Med. Genet. A
, vol.122
, pp. 42-45
-
-
Wollnik, B.1
-
185
-
-
0032938813
-
A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo
-
Yamaguchi T.P., et al. A Wnt5a pathway underlies outgrowth of multiple structures in the vertebrate embryo. Development 126 (1999) 1211-1223
-
(1999)
Development
, vol.126
, pp. 1211-1223
-
-
Yamaguchi, T.P.1
-
186
-
-
0023214676
-
Is disordered folate metabolism the basis for the genetic predisposition to neural tube defects?
-
Yates J.R., et al. Is disordered folate metabolism the basis for the genetic predisposition to neural tube defects?. Clin. Genet. 31 (1987) 279-287
-
(1987)
Clin. Genet.
, vol.31
, pp. 279-287
-
-
Yates, J.R.1
-
187
-
-
0036333373
-
Sonic hedgehog and the molecular regulation of mouse neural tube closure
-
Ybot-Gonzalez P., et al. Sonic hedgehog and the molecular regulation of mouse neural tube closure. Development 129 (2002) 2507-2517
-
(2002)
Development
, vol.129
, pp. 2507-2517
-
-
Ybot-Gonzalez, P.1
-
188
-
-
33947304005
-
Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure
-
Ybot-Gonzalez P., et al. Convergent extension, planar-cell-polarity signalling and initiation of mouse neural tube closure. Development 134 (2007) 789-799
-
(2007)
Development
, vol.134
, pp. 789-799
-
-
Ybot-Gonzalez, P.1
-
189
-
-
0031569359
-
Evidence that absence of Wnt-3a signaling promotes neuralization instead of paraxial mesoderm development in the mouse
-
Yoshikawa Y., et al. Evidence that absence of Wnt-3a signaling promotes neuralization instead of paraxial mesoderm development in the mouse. Dev. Biol. 183 (1997) 234-242
-
(1997)
Dev. Biol.
, vol.183
, pp. 234-242
-
-
Yoshikawa, Y.1
-
190
-
-
33749524559
-
The Grainyhead-like epithelial transactivator Get-1/Grhl3 regulates epidermal terminal differentiation and interacts functionally with LMO4
-
Yu Z., et al. The Grainyhead-like epithelial transactivator Get-1/Grhl3 regulates epidermal terminal differentiation and interacts functionally with LMO4. Dev. Biol. 299 (2006) 122-136
-
(2006)
Dev. Biol.
, vol.299
, pp. 122-136
-
-
Yu, Z.1
-
191
-
-
0029946542
-
Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene
-
Zhao Q., et al. Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene. Nat. Genet. 13 (1996) 275-283
-
(1996)
Nat. Genet.
, vol.13
, pp. 275-283
-
-
Zhao, Q.1
-
192
-
-
0347931742
-
Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects
-
Zhu H., et al. Promoter haplotype combinations for the human PDGFRA gene are associated with risk of neural tube defects. Mol. Genet. Metab. 81 (2004) 127-132
-
(2004)
Mol. Genet. Metab.
, vol.81
, pp. 127-132
-
-
Zhu, H.1
-
193
-
-
0028952247
-
Homozygosity for Waardenburg syndrome
-
Zlotogora J., et al. Homozygosity for Waardenburg syndrome. Am. J. Hum. Genet. 56 (1995) 1173-1178
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 1173-1178
-
-
Zlotogora, J.1
-
194
-
-
26444530096
-
Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse
-
Zohn I.E., et al. Using genomewide mutagenesis screens to identify the genes required for neural tube closure in the mouse. Birth Defects Res. A Clin. Mol. Teratol. 73 (2005) 583-590
-
(2005)
Birth Defects Res. A Clin. Mol. Teratol.
, vol.73
, pp. 583-590
-
-
Zohn, I.E.1
-
195
-
-
33744544424
-
P38 and a p38-interacting protein are critical for downregulation of E-cadherin during mouse gastrulation
-
Zohn I.E., et al. P38 and a p38-interacting protein are critical for downregulation of E-cadherin during mouse gastrulation. Cell 125 (2006) 957-969
-
(2006)
Cell
, vol.125
, pp. 957-969
-
-
Zohn, I.E.1
-
196
-
-
34249671135
-
The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure
-
Zohn I.E., et al. The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure. Dev. Biol. 306 (2007) 208-221
-
(2007)
Dev. Biol.
, vol.306
, pp. 208-221
-
-
Zohn, I.E.1
|