-
1
-
-
0033973033
-
High-dose folic acid supplementation in rats: effects on gestation and the methionine cycle
-
Achon M., Alonso-Aperte E., Reyes L., Ubeda N., Varela-Moreiras G. High-dose folic acid supplementation in rats: effects on gestation and the methionine cycle. Br. J. Nutr. 2000, 83:177-183.
-
(2000)
Br. J. Nutr.
, vol.83
, pp. 177-183
-
-
Achon, M.1
Alonso-Aperte, E.2
Reyes, L.3
Ubeda, N.4
Varela-Moreiras, G.5
-
2
-
-
0034754798
-
Severe nasal clefting and abnormal embryonic apoptosis in Alx3/Alx4 double mutant mice
-
Beverdam A., Brouwer A., Reijnen M., Korving J., Meijlink F. Severe nasal clefting and abnormal embryonic apoptosis in Alx3/Alx4 double mutant mice. Development 2001, 128:3975-3986.
-
(2001)
Development
, vol.128
, pp. 3975-3986
-
-
Beverdam, A.1
Brouwer, A.2
Reijnen, M.3
Korving, J.4
Meijlink, F.5
-
3
-
-
0034885382
-
Expression patterns of group-I aristaless-related genes during craniofacial and limb development
-
Beverdam A., Meijlink F. Expression patterns of group-I aristaless-related genes during craniofacial and limb development. Mech. Dev. 2001, 107:163-167.
-
(2001)
Mech. Dev.
, vol.107
, pp. 163-167
-
-
Beverdam, A.1
Meijlink, F.2
-
4
-
-
33747588534
-
Neural tube defects and folate: case far from closed
-
Blom H.J., Shaw G.M., den Heijer M., Finnell R.H. Neural tube defects and folate: case far from closed. Nat. Rev. Neurosci. 2006, 7:724-731.
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 724-731
-
-
Blom, H.J.1
Shaw, G.M.2
den Heijer, M.3
Finnell, R.H.4
-
5
-
-
65449148808
-
Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study
-
Boyles A.L., Wilcox A.J., Taylor J.A., Shi M., Weinberg C.R., Meyer K., Fredriksen A., Ueland P.M., Johansen A.M.W., Drevon C.A., Jugessur A., Trung T.N., Gjessing H.K., Vollset S.E., Murray J.C., Christensen K., Lie R.T. Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study. Genet. Epidemiol. 2009, 33:247-255.
-
(2009)
Genet. Epidemiol.
, vol.33
, pp. 247-255
-
-
Boyles, A.L.1
Wilcox, A.J.2
Taylor, J.A.3
Shi, M.4
Weinberg, C.R.5
Meyer, K.6
Fredriksen, A.7
Ueland, P.M.8
Johansen, A.M.W.9
Drevon, C.A.10
Jugessur, A.11
Trung, T.N.12
Gjessing, H.K.13
Vollset, S.E.14
Murray, J.C.15
Christensen, K.16
Lie, R.T.17
-
6
-
-
0024545897
-
Teratogenic interaction of folic acid and zinc deficiencies in the rat
-
Bremert J.C., Dreosti I.E., Tulsi R.S. Teratogenic interaction of folic acid and zinc deficiencies in the rat. Nutr. Rep. Int. 1989, 38:383-390.
-
(1989)
Nutr. Rep. Int.
, vol.38
, pp. 383-390
-
-
Bremert, J.C.1
Dreosti, I.E.2
Tulsi, R.S.3
-
7
-
-
0036245188
-
Investigation of the effects of folate deficiency on embryonic development through the establishment of a folate deficient mouse model
-
Burgoon J.M., Selhub J., Nadeau M., Sadler T.W. Investigation of the effects of folate deficiency on embryonic development through the establishment of a folate deficient mouse model. Teratology 2002, 65:219-227.
-
(2002)
Teratology
, vol.65
, pp. 219-227
-
-
Burgoon, J.M.1
Selhub, J.2
Nadeau, M.3
Sadler, T.W.4
-
8
-
-
56049094808
-
Gene-environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 function
-
Burren K.A., Savery D., Massa V., Kok R.M., Scott J.M., Blom H.J., Copp A.J., Greene N.D.E. Gene-environment interactions in the causation of neural tube defects: folate deficiency increases susceptibility conferred by loss of Pax3 function. Hum. Mol. Genet. 2008, 17:3675-3685.
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. 3675-3685
-
-
Burren, K.A.1
Savery, D.2
Massa, V.3
Kok, R.M.4
Scott, J.M.5
Blom, H.J.6
Copp, A.J.7
Greene, N.D.E.8
-
9
-
-
0035282903
-
Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition
-
Chen Z., Karaplis A.C., Ackerman S.L., Pogribny I.P., Melnyk S., Lussier-Cacan S., Chen M.F., Pai A., John S.W.M., Smith R.S., Bottiglieri T., Bagley P., Selhub J., Rudnicki M.A., James S.J., Rozen R. Mice deficient in methylenetetrahydrofolate reductase exhibit hyperhomocysteinemia and decreased methylation capacity, with neuropathology and aortic lipid deposition. Hum. Mol. Genet. 2001, 10:433-443.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 433-443
-
-
Chen, Z.1
Karaplis, A.C.2
Ackerman, S.L.3
Pogribny, I.P.4
Melnyk, S.5
Lussier-Cacan, S.6
Chen, M.F.7
Pai, A.8
John, S.W.M.9
Smith, R.S.10
Bottiglieri, T.11
Bagley, P.12
Selhub, J.13
Rudnicki, M.A.14
James, S.J.15
Rozen, R.16
-
10
-
-
0028933142
-
Twist is required in head mesenchyme for cranial neural tube morphogenesis
-
Chen Z.F., Behringer R.R. twist is required in head mesenchyme for cranial neural tube morphogenesis. Genes Dev. 1995, 9:686-699.
-
(1995)
Genes Dev.
, vol.9
, pp. 686-699
-
-
Chen, Z.F.1
Behringer, R.R.2
-
11
-
-
0002984191
-
Dissection and culture of postimplantation embryos
-
Oxford University Press, Oxford, A.J. Copp, D.L. Cockroft (Eds.)
-
Cockroft D.L. Dissection and culture of postimplantation embryos. Postimplanation Mammalian Embryos. A Practical Approach 1990, 15-40. Oxford University Press, Oxford. A.J. Copp, D.L. Cockroft (Eds.).
-
(1990)
Postimplanation Mammalian Embryos. A Practical Approach
, pp. 15-40
-
-
Cockroft, D.L.1
-
12
-
-
28444460247
-
Neurulation in the cranial region - normal and abnormal
-
Copp A.J. Neurulation in the cranial region - normal and abnormal. J. Anat. 2005, 207:623-635.
-
(2005)
J. Anat.
, vol.207
, pp. 623-635
-
-
Copp, A.J.1
-
14
-
-
0027080461
-
Prevention of the first occurrence of neural tube defects by periconceptional vitamin supplementation
-
Czeizel A.E., Dudas I. Prevention of the first occurrence of neural tube defects by periconceptional vitamin supplementation. N. Engl J. Med. 1992, 327:1832-1835.
-
(1992)
N. Engl J. Med.
, vol.327
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
15
-
-
33750039987
-
Current perspectives on the genetic causes of neural tube defects
-
De Marco P., Merello E., Mascelli S., Capra V. Current perspectives on the genetic causes of neural tube defects. Neurogenetics 2006, 7:201-221.
-
(2006)
Neurogenetics
, vol.7
, pp. 201-221
-
-
De Marco, P.1
Merello, E.2
Mascelli, S.3
Capra, V.4
-
16
-
-
0032568871
-
Embryonic folate metabolism and mouse neural tube defects
-
Fleming A., Copp A. Embryonic folate metabolism and mouse neural tube defects. Science 1998, 280:2107-2109.
-
(1998)
Science
, vol.280
, pp. 2107-2109
-
-
Fleming, A.1
Copp, A.2
-
17
-
-
0034161971
-
A genetic risk factor for mouse neural tube defects: defining the embryonic basis
-
Fleming A., Copp A.J. A genetic risk factor for mouse neural tube defects: defining the embryonic basis. Hum. Mol. Genet. 2000, 9:575-581.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 575-581
-
-
Fleming, A.1
Copp, A.J.2
-
18
-
-
0038412822
-
The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase
-
Fuks F., Hurd P.J., Deplus R., Kouzarides T. The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase. Nucleic Acids Res. 2003, 31:2305-2312.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 2305-2312
-
-
Fuks, F.1
Hurd, P.J.2
Deplus, R.3
Kouzarides, T.4
-
19
-
-
0036829654
-
Functional domains of paired-like homeoprotein Cart1 and the relationship between dimerization and transcription activity
-
Furukawa K., Lioka T., Morishita M., Yamaguchi A., Shindo H., Namba H., Yamashita S., Tsukazaki T. Functional domains of paired-like homeoprotein Cart1 and the relationship between dimerization and transcription activity. Genes Cells 2002, 7:1135-1147.
-
(2002)
Genes Cells
, vol.7
, pp. 1135-1147
-
-
Furukawa, K.1
Lioka, T.2
Morishita, M.3
Yamaguchi, A.4
Shindo, H.5
Namba, H.6
Yamashita, S.7
Tsukazaki, T.8
-
20
-
-
47749100055
-
Embryonic development in the reduced folate carrier knockout mouse is modulated by maternal folate supplementation
-
Gelineau-van Waes J., Heller S., Bauer L.K., Wilberding J., Maddox J.R., Aleman F., Rosenquist T.H., Finnell R.H. Embryonic development in the reduced folate carrier knockout mouse is modulated by maternal folate supplementation. Birth Defects Res. A 2008, 82:494-507.
-
(2008)
Birth Defects Res. A
, vol.82
, pp. 494-507
-
-
Gelineau-van Waes, J.1
Heller, S.2
Bauer, L.K.3
Wilberding, J.4
Maddox, J.R.5
Aleman, F.6
Rosenquist, T.H.7
Finnell, R.H.8
-
21
-
-
33646819033
-
A folate- and methyl-deficient diet alters the expression of DNA methyltransferases and methyl CpG binding proteins involved in epigenetic gene silencing in livers of F344 rats
-
Ghoshal K., Li X., Datta J., Bai S., Pogribny M., Huang Y., Young D., Jacob S.T. A folate- and methyl-deficient diet alters the expression of DNA methyltransferases and methyl CpG binding proteins involved in epigenetic gene silencing in livers of F344 rats. J. Nutr. 2006, 136:1522-1527.
-
(2006)
J. Nutr.
, vol.136
, pp. 1522-1527
-
-
Ghoshal, K.1
Li, X.2
Datta, J.3
Bai, S.4
Pogribny, M.5
Huang, Y.6
Young, D.7
Jacob, S.T.8
-
22
-
-
0022339117
-
A review of the theories of the vertebrate neurulation and their relationship to the mechanics of neural tube birth defects
-
Gordon R. A review of the theories of the vertebrate neurulation and their relationship to the mechanics of neural tube birth defects. J. Embryol. Exp. Morphol. 1985, 89:229-255.
-
(1985)
J. Embryol. Exp. Morphol.
, vol.89
, pp. 229-255
-
-
Gordon, R.1
-
23
-
-
0031033593
-
Inositol prevents folate-resistant neural tube defects in the mouse
-
Greene N.D.E., Copp A.J. Inositol prevents folate-resistant neural tube defects in the mouse. Nat. Med. 1997, 3:60-66.
-
(1997)
Nat. Med.
, vol.3
, pp. 60-66
-
-
Greene, N.D.E.1
Copp, A.J.2
-
24
-
-
64849104728
-
Development of the vertebrate central nervous system: formation of the neural tube
-
Greene N.D.E., Copp A.J. Development of the vertebrate central nervous system: formation of the neural tube. Prenat. Diagn. 2009, 29:303-311.
-
(2009)
Prenat. Diagn.
, vol.29
, pp. 303-311
-
-
Greene, N.D.E.1
Copp, A.J.2
-
25
-
-
1342282910
-
Defective neural tube closure and anteroposterior patterning in mice lacking the LIM protein LMO4 or its interacting partner Deaf-1
-
Hahm K., Sum E.Y.M., Fujiwara Y., Lindeman G., Visvader J.E., Orkin S.H. Defective neural tube closure and anteroposterior patterning in mice lacking the LIM protein LMO4 or its interacting partner Deaf-1. Mol. Cell. Biol. 2004, 24:2074-2082.
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 2074-2082
-
-
Hahm, K.1
Sum, E.Y.M.2
Fujiwara, Y.3
Lindeman, G.4
Visvader, J.E.5
Orkin, S.H.6
-
26
-
-
0035003372
-
Why are the genes that cause risk of human neural tube defects so hard to find?
-
Harris M.J. Why are the genes that cause risk of human neural tube defects so hard to find?. Teratology 2001, 63:165-166.
-
(2001)
Teratology
, vol.63
, pp. 165-166
-
-
Harris, M.J.1
-
27
-
-
33947172588
-
Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects
-
Harris M.J., Juriloff D.M. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects. Birth Defects Res. A 2007, 79:187-210.
-
(2007)
Birth Defects Res. A
, vol.79
, pp. 187-210
-
-
Harris, M.J.1
Juriloff, D.M.2
-
28
-
-
0026554901
-
Folate deficiency alone does not produce neural tube defects in mice
-
Heid M.K., Bills N.D., Hinrichs S.H., Clifford A.J. Folate deficiency alone does not produce neural tube defects in mice. J. Nutr. 1992, 122:888-894.
-
(1992)
J. Nutr.
, vol.122
, pp. 888-894
-
-
Heid, M.K.1
Bills, N.D.2
Hinrichs, S.H.3
Clifford, A.J.4
-
29
-
-
0035362582
-
Neural tube defects and neuroepithelial cell death in Tupl3 knockout mice
-
Ikeda A., Ikeda S., Gridley T., Nishina P., Naggert J. Neural tube defects and neuroepithelial cell death in Tupl3 knockout mice. Hum. Mol. Genet. 2001, 10:1325-1334.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1325-1334
-
-
Ikeda, A.1
Ikeda, S.2
Gridley, T.3
Nishina, P.4
Naggert, J.5
-
30
-
-
34249656278
-
The murine allantois: emerging paradigms of the mammalian umbilical cord and its relation to the fetus
-
Inman K.E., Downs K.M. The murine allantois: emerging paradigms of the mammalian umbilical cord and its relation to the fetus. Genesis 2007, 45:237-258.
-
(2007)
Genesis
, vol.45
, pp. 237-258
-
-
Inman, K.E.1
Downs, K.M.2
-
31
-
-
65549094033
-
Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia
-
Jugessur A., Shi M., Gjessing H.K., Lie R.T., Wilcox A.J., Weinberg C.R., Christensen K., Boyles A.L., Daack-Hirsch S., Trung T.N., Bille C., Lidral A.C., Murray J.C. Genetic determinants of facial clefting: analysis of 357 candidate genes using two national cleft studies from Scandinavia. PLoS ONE 2009, 4:e5385. 10.1371/journal.pone.0005385.
-
(2009)
PLoS ONE
, vol.4
-
-
Jugessur, A.1
Shi, M.2
Gjessing, H.K.3
Lie, R.T.4
Wilcox, A.J.5
Weinberg, C.R.6
Christensen, K.7
Boyles, A.L.8
Daack-Hirsch, S.9
Trung, T.N.10
Bille, C.11
Lidral, A.C.12
Murray, J.C.13
-
32
-
-
0025807774
-
Normal mouse strains differ in the site of initiation of closure of the cranial neural tube
-
Juriloff D.M., Harris M.J., Tom C., MacDonald K.B. Normal mouse strains differ in the site of initiation of closure of the cranial neural tube. Teratology 1991, 44:225-233.
-
(1991)
Teratology
, vol.44
, pp. 225-233
-
-
Juriloff, D.M.1
Harris, M.J.2
Tom, C.3
MacDonald, K.B.4
-
33
-
-
34247570440
-
Toward understanding the genetic basis of neural tube defects
-
Kibar Z., Capra V., Gros P. Toward understanding the genetic basis of neural tube defects. Clin. Genet. 2007, 71:295-310.
-
(2007)
Clin. Genet.
, vol.71
, pp. 295-310
-
-
Kibar, Z.1
Capra, V.2
Gros, P.3
-
34
-
-
34047261773
-
Mutations in VANGL1 associated with neural-tube defects
-
Kibar Z., Torban E., McDearmid J.R., Reynolds A., Berghout J., Mathieu M., Kirillova I., De Marco P., Merello E., Hayes J.M., Wallingford J.B., Drapeau P., Capra V., Gros P. Mutations in VANGL1 associated with neural-tube defects. N. Engl J. Med. 2007, 356:1432-1437.
-
(2007)
N. Engl J. Med.
, vol.356
, pp. 1432-1437
-
-
Kibar, Z.1
Torban, E.2
McDearmid, J.R.3
Reynolds, A.4
Berghout, J.5
Mathieu, M.6
Kirillova, I.7
De Marco, P.8
Merello, E.9
Hayes, J.M.10
Wallingford, J.B.11
Drapeau, P.12
Capra, V.13
Gros, P.14
-
35
-
-
2942574352
-
Folate and DNA methylation: a mechanistic link between folate deficiency and colorectal cancer?
-
Kim Y.I. Folate and DNA methylation: a mechanistic link between folate deficiency and colorectal cancer?. Cancer Epidem. Biomar. 2004, 13:511-519.
-
(2004)
Cancer Epidem. Biomar.
, vol.13
, pp. 511-519
-
-
Kim, Y.I.1
-
36
-
-
0036245044
-
Exencephaly in a subset of animals heterozygous for AP-2alpha mutation
-
Kohlbecker A., Lee A.E., Schorle H. Exencephaly in a subset of animals heterozygous for AP-2alpha mutation. Teratology 2002, 65:213-218.
-
(2002)
Teratology
, vol.65
, pp. 213-218
-
-
Kohlbecker, A.1
Lee, A.E.2
Schorle, H.3
-
37
-
-
33745632810
-
Dlx homeobox gene control of mammalian limb and craniofacial development
-
Kraus P., Lufkin T. Dlx homeobox gene control of mammalian limb and craniofacial development. Am. J. Med. Genet. A 2006, 140A:1366-1374.
-
(2006)
Am. J. Med. Genet. A
, vol.140 A
, pp. 1366-1374
-
-
Kraus, P.1
Lufkin, T.2
-
38
-
-
17744376805
-
Genetics of shoulder girdle formation: roles of Tbx15 and aristaless-like genes
-
Kuijper S., Beverdam A., Kroon C., Brouwer A., Candille S., Barsh G., Meijlink F. Genetics of shoulder girdle formation: roles of Tbx15 and aristaless-like genes. Development 2005, 132:1601-1610.
-
(2005)
Development
, vol.132
, pp. 1601-1610
-
-
Kuijper, S.1
Beverdam, A.2
Kroon, C.3
Brouwer, A.4
Candille, S.5
Barsh, G.6
Meijlink, F.7
-
39
-
-
0036322759
-
Isolation of differentially expressed genes from wild-type and Twist mutant mouse limb buds
-
Loebel D.A.F., O'Rourke M.P., Steiner K.A., Banyer J., Tam P.P.L. Isolation of differentially expressed genes from wild-type and Twist mutant mouse limb buds. Genesis 2002, 33:103-113.
-
(2002)
Genesis
, vol.33
, pp. 103-113
-
-
Loebel, D.A.F.1
O'Rourke, M.P.2
Steiner, K.A.3
Banyer, J.4
Tam, P.P.L.5
-
40
-
-
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. 2005, 135C:77-87.
-
(2005)
Am. J. Med. Genet.
, vol.135 C
, pp. 77-87
-
-
Loeken, M.R.1
-
41
-
-
58149263382
-
A composite intronic element directs dynamic binding of the progesterone receptor and GATA-2
-
Magklara A., Smith C.L. A composite intronic element directs dynamic binding of the progesterone receptor and GATA-2. Mol. Endocrinol. 2009, 23:61-73.
-
(2009)
Mol. Endocrinol.
, vol.23
, pp. 61-73
-
-
Magklara, A.1
Smith, C.L.2
-
42
-
-
0036471326
-
Folic acid prevents exencephaly in Cited2 deficient mice
-
Martinez-Barbera J.P., Rodriguez T.A., Greene N.D., Weninger W.J., Simeone A., Copp A.J., Beddington R.S., Dunwoodie S. Folic acid prevents exencephaly in Cited2 deficient mice. Hum. Mol. Genet. 2002, 11:283-293.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 283-293
-
-
Martinez-Barbera, J.P.1
Rodriguez, T.A.2
Greene, N.D.3
Weninger, W.J.4
Simeone, A.5
Copp, A.J.6
Beddington, R.S.7
Dunwoodie, S.8
-
43
-
-
0033570336
-
Astroglial differentiation of cortical precursor cells triggered by activation of the cAMP-dependent signaling pathway
-
McManus M.F., Chen L.C., Vallejo I., Vallejo M. Astroglial differentiation of cortical precursor cells triggered by activation of the cAMP-dependent signaling pathway. J. Neurosci. 1999, 19:9004-9015.
-
(1999)
J. Neurosci.
, vol.19
, pp. 9004-9015
-
-
McManus, M.F.1
Chen, L.C.2
Vallejo, I.3
Vallejo, M.4
-
44
-
-
0033370681
-
Vertebrate aristaless-related genes
-
Meijlink F., Beverdam A., Brouwer A., Oosterveen T.C., Ten Berge D. Vertebrate aristaless-related genes. Int. J. Dev. Biol. 1999, 43:651-663.
-
(1999)
Int. J. Dev. Biol.
, vol.43
, pp. 651-663
-
-
Meijlink, F.1
Beverdam, A.2
Brouwer, A.3
Oosterveen, T.C.4
Ten Berge, D.5
-
45
-
-
0024598208
-
Growth of 9.5-day rat embryos in folic-acid-deficient serum
-
Miller P.N., Pratten M.K., Beck F. Growth of 9.5-day rat embryos in folic-acid-deficient serum. Teratology 1989, 39:375-385.
-
(1989)
Teratology
, vol.39
, pp. 375-385
-
-
Miller, P.N.1
Pratten, M.K.2
Beck, F.3
-
46
-
-
33751552385
-
The homeoprotein Alx3 expressed in pancreatic b-cells regulates insulin gene transcription by interacting with the basic helix-loop-helix protein E47
-
Mirasierra M., Vallejo M. The homeoprotein Alx3 expressed in pancreatic b-cells regulates insulin gene transcription by interacting with the basic helix-loop-helix protein E47. Mol. Endocrinol. 2006, 20:2876-2889.
-
(2006)
Mol. Endocrinol.
, vol.20
, pp. 2876-2889
-
-
Mirasierra, M.1
Vallejo, M.2
-
47
-
-
0018198741
-
Regional differences in mesenchymal cell morphology and glycosaminoglycans in early neural-fold stage rat embryos
-
Morriss G.M., Solursh M. Regional differences in mesenchymal cell morphology and glycosaminoglycans in early neural-fold stage rat embryos. J. Embryol. Exp. Morphol. 1978, 46:37-52.
-
(1978)
J. Embryol. Exp. Morphol.
, vol.46
, pp. 37-52
-
-
Morriss, G.M.1
Solursh, M.2
-
48
-
-
1842288286
-
The role of primary mesenchyme in normal and abnormal morphogenesis of mammalian neural folds
-
Morriss G.M., Solursh M. The role of primary mesenchyme in normal and abnormal morphogenesis of mammalian neural folds. Zoon 1978, 6:33-38.
-
(1978)
Zoon
, vol.6
, pp. 33-38
-
-
Morriss, G.M.1
Solursh, M.2
-
49
-
-
0029692152
-
In situ hybridization analysis of chick embryos in whole mount and tissue sections
-
Nieto M.A., Patel K., Wilkinson D.G. In situ hybridization analysis of chick embryos in whole mount and tissue sections. Meth. Cell Biol. 1996, 51:219-235.
-
(1996)
Meth. Cell Biol.
, vol.51
, pp. 219-235
-
-
Nieto, M.A.1
Patel, K.2
Wilkinson, D.G.3
-
50
-
-
0036130683
-
The two sites of fusion of the neural folds and the two neuropores in the human embryo
-
O'Rahilly R., Muller F. The two sites of fusion of the neural folds and the two neuropores in the human embryo. Teratology 2002, 65:162-170.
-
(2002)
Teratology
, vol.65
, pp. 162-170
-
-
O'Rahilly, R.1
Muller, F.2
-
51
-
-
0036369030
-
Twist functions in mouse development
-
O'Rourke M.P., Tam P.P.L. Twist functions in mouse development. Int. J. Dev. Biol. 2002, 46:401-413.
-
(2002)
Int. J. Dev. Biol.
, vol.46
, pp. 401-413
-
-
O'Rourke, M.P.1
Tam, P.P.L.2
-
52
-
-
0036723777
-
Polymorphic susceptibility to the molecular causes of neural tube defects during diabetic embryopathy
-
Pani L., Horal M., Loeken M.R. Polymorphic susceptibility to the molecular causes of neural tube defects during diabetic embryopathy. Diabetes 2002, 51:2871-2874.
-
(2002)
Diabetes
, vol.51
, pp. 2871-2874
-
-
Pani, L.1
Horal, M.2
Loeken, M.R.3
-
53
-
-
4444293956
-
The homeoprotein Alx3 contains discrete functional domains and exhibits cell-specific and selective monomeric binding and transactivation
-
Perez-Villamil B., Mirasierra M., Vallejo M. The homeoprotein Alx3 contains discrete functional domains and exhibits cell-specific and selective monomeric binding and transactivation. J. Biol. Chem. 2004, 279:38062-38071.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 38062-38071
-
-
Perez-Villamil, B.1
Mirasierra, M.2
Vallejo, M.3
-
54
-
-
0032884078
-
Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development
-
Piedrahita J.A., Oetama B., Bennett G.D., van Waes J., Kamen B.A., Richardson J., Lacey S.W., Anderson R.G., Finnell R.H. Mice lacking the folic acid-binding protein Folbp1 are defective in early embryonic development. Nat. Genet. 1999, 23:228-232.
-
(1999)
Nat. Genet.
, vol.23
, pp. 228-232
-
-
Piedrahita, J.A.1
Oetama, B.2
Bennett, G.D.3
van Waes, J.4
Kamen, B.A.5
Richardson, J.6
Lacey, S.W.7
Anderson, R.G.8
Finnell, R.H.9
-
55
-
-
0032915190
-
Physical and genetic interactions between Alx4 and Cart1
-
Qu S., Tucker S.C., Zhai Q., de Crombrugghe B., Wisdom R. Physical and genetic interactions between Alx4 and Cart1. Development 1999, 126:359-369.
-
(1999)
Development
, vol.126
, pp. 359-369
-
-
Qu, S.1
Tucker, S.C.2
Zhai, Q.3
de Crombrugghe, B.4
Wisdom, R.5
-
56
-
-
0029617650
-
Fibroblast growth factor 2 increases Otx2 expression in precursor cells from mammalian telencephalon
-
Robel L., Ding M., James A.J., Lin X., Simeone A., Leckman J.F., Vaccarino F.M. Fibroblast growth factor 2 increases Otx2 expression in precursor cells from mammalian telencephalon. J. Neurosci. 1995, 15:7879-7891.
-
(1995)
J. Neurosci.
, vol.15
, pp. 7879-7891
-
-
Robel, L.1
Ding, M.2
James, A.J.3
Lin, X.4
Simeone, A.5
Leckman, J.F.6
Vaccarino, F.M.7
-
57
-
-
0037217759
-
Spatial and temporal expression of folate-binding protein 1 (Fbp1) is closely associated with anterior neural tube closure in mice
-
Saitsu H., Ishibashi M., Nakano H., Shiota K. Spatial and temporal expression of folate-binding protein 1 (Fbp1) is closely associated with anterior neural tube closure in mice. Dev. Dyn. 2003, 226:112-117.
-
(2003)
Dev. Dyn.
, vol.226
, pp. 112-117
-
-
Saitsu, H.1
Ishibashi, M.2
Nakano, H.3
Shiota, K.4
-
58
-
-
0029932086
-
Transcription factor AP-2 essential for cranial closure and craniofacial development
-
Schorle H., Meier P., Buchert M., Jaenisch R., Mitchell P.J. Transcription factor AP-2 essential for cranial closure and craniofacial development. Nature 1996, 38:235-238.
-
(1996)
Nature
, vol.38
, pp. 235-238
-
-
Schorle, H.1
Meier, P.2
Buchert, M.3
Jaenisch, R.4
Mitchell, P.J.5
-
59
-
-
0039595012
-
Pancreatic homeodomain transcription factor IDX1/IPF1 expressed in developing brain regulates somatostatin gene transcription in embryonic neural cells
-
Schwartz P.T., Perez-Villamil B., Rivera A., Moratalla R., Vallejo M. Pancreatic homeodomain transcription factor IDX1/IPF1 expressed in developing brain regulates somatostatin gene transcription in embryonic neural cells. J. Biol. Chem. 2000, 275:19106-19114.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 19106-19114
-
-
Schwartz, P.T.1
Perez-Villamil, B.2
Rivera, A.3
Moratalla, R.4
Vallejo, M.5
-
60
-
-
0036308745
-
Twist function is required for the morphogenesis of the cephalic neural tube and the differentiation of the cranial neural crest cells in the mouse embryo
-
Soo K., O'Rourke M.P., Khoo P.L., Steiner K.A., Wong N., Behringer R.R., Tam P.P.L. Twist function is required for the morphogenesis of the cephalic neural tube and the differentiation of the cranial neural crest cells in the mouse embryo. Dev. Biol. 2002, 247:251-270.
-
(2002)
Dev. Biol.
, vol.247
, pp. 251-270
-
-
Soo, K.1
O'Rourke, M.P.2
Khoo, P.L.3
Steiner, K.A.4
Wong, N.5
Behringer, R.R.6
Tam, P.P.L.7
-
61
-
-
0032105472
-
Mouse Alx3: an aristaless-like homeobox gene expressed during embryogenesis in ectomesenchyme and lateral plate mesoderm
-
ten Berge D., Brouwer A., el Bahi S., Guenet J.L., Robert B., Meijlink F. Mouse Alx3: an aristaless-like homeobox gene expressed during embryogenesis in ectomesenchyme and lateral plate mesoderm. Dev. Biol. 1998, 199:11-25.
-
(1998)
Dev. Biol.
, vol.199
, pp. 11-25
-
-
ten Berge, D.1
Brouwer, A.2
el Bahi, S.3
Guenet, J.L.4
Robert, B.5
Meijlink, F.6
-
62
-
-
65149104203
-
Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene
-
Twigg S.R.F., Versnel S.L., Nurnberg G., Lees M.M., Bhat M., Hammond P., Hennekam C.M., Hoogeboom A.J.M., Hurst J.A., Johnson D., Robinson A.A., Scambler P.J., Gerrelli D., Nurnberg P., Mathijssen I.M.J., Wilkie A.O.M. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. Am. J. Hum. Genet. 2009, 84:1-8.
-
(2009)
Am. J. Hum. Genet.
, vol.84
, pp. 1-8
-
-
Twigg, S.R.F.1
Versnel, S.L.2
Nurnberg, G.3
Lees, M.M.4
Bhat, M.5
Hammond, P.6
Hennekam, C.M.7
Hoogeboom, A.J.M.8
Hurst, J.A.9
Johnson, D.10
Robinson, A.A.11
Scambler, P.J.12
Gerrelli, D.13
Nurnberg, P.14
Mathijssen, I.M.J.15
Wilkie, A.O.M.16
-
63
-
-
33847259704
-
A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3
-
Uyguner O., Kayserili H., Li Y., Karaman B., Nurnberg G., Hennies H.C., Becker C., Nurnberg P., Basaran S., Apak M.Y., Wollnik B. A new locus for autosomal recessive non-syndromic mental retardation maps to 1p21.1-p13.3. Clin. Genet. 2007, 71:212-219.
-
(2007)
Clin. Genet.
, vol.71
, pp. 212-219
-
-
Uyguner, O.1
Kayserili, H.2
Li, Y.3
Karaman, B.4
Nurnberg, G.5
Hennies, H.C.6
Becker, C.7
Nurnberg, P.8
Basaran, S.9
Apak, M.Y.10
Wollnik, B.11
-
64
-
-
0030589702
-
Lineage-specific regulation of the neural differentiation gene MASH1
-
Verma-Kurvari S., Savage T., Gowan K., Johnson J.E. Lineage-specific regulation of the neural differentiation gene MASH1. Dev. Biol. 1996, 180:605-617.
-
(1996)
Dev. Biol.
, vol.180
, pp. 605-617
-
-
Verma-Kurvari, S.1
Savage, T.2
Gowan, K.3
Johnson, J.E.4
-
65
-
-
0025863475
-
Prevention of neural tube defects: results of the Medical Research Council Vitamin Study
-
Group, M.V.S.R
-
Wald N., Sneddon J., Densem J., Frost C., Stone R. Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet 1991, 338:131-137. Group, M.V.S.R.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
Wald, N.1
Sneddon, J.2
Densem, J.3
Frost, C.4
Stone, R.5
-
66
-
-
33847786727
-
Folic acid supplements and risk of facial clefts: national population based case-control study
-
Willcox A.J., Lie R.T., Solvoll K., Taylor J., McConnaughey D.R., Abyholm F., Vindenes H., Vollset S.E., Drevon C.A. Folic acid supplements and risk of facial clefts: national population based case-control study. Br. Med. J. 2007, 334:464-469.
-
(2007)
Br. Med. J.
, vol.334
, pp. 464-469
-
-
Willcox, A.J.1
Lie, R.T.2
Solvoll, K.3
Taylor, J.4
McConnaughey, D.R.5
Abyholm, F.6
Vindenes, H.7
Vollset, S.E.8
Drevon, C.A.9
-
67
-
-
0036161759
-
Combined restriction landmark genomic scanning and virtual genome scans identify a novel human homeobox gene, ALX3, that is hypermethylated in neuroblastoma
-
Wimmer K., Zhu X.X., Rouillard J.M., Ambros P.F., Lamb B.J., Kuick R., Eckart M., Weinhausl A., Fonatsh C., Hanash S.M. Combined restriction landmark genomic scanning and virtual genome scans identify a novel human homeobox gene, ALX3, that is hypermethylated in neuroblastoma. Genes Chromosom. Cancer 2002, 33:285-294.
-
(2002)
Genes Chromosom. Cancer
, vol.33
, pp. 285-294
-
-
Wimmer, K.1
Zhu, X.X.2
Rouillard, J.M.3
Ambros, P.F.4
Lamb, B.J.5
Kuick, R.6
Eckart, M.7
Weinhausl, A.8
Fonatsh, C.9
Hanash, S.M.10
-
68
-
-
0029946542
-
Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene
-
Zhao Q., Behringer R.R., Crombrugghe Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene. Nat. Genet. 1996, 13:275-283.
-
(1996)
Nat. Genet.
, vol.13
, pp. 275-283
-
-
Zhao, Q.1
Behringer, R.R.2
Crombrugghe3
-
69
-
-
0032478826
-
A reduced folate carrier mutation produces substrate-dependent alterations in carrier mobility in murine leukemia cells and methotrexate resistance with conservation of growth in 5-formyltetrahydrofolate
-
Zhao R., Assaraf Y.G., Goldman I.D. A reduced folate carrier mutation produces substrate-dependent alterations in carrier mobility in murine leukemia cells and methotrexate resistance with conservation of growth in 5-formyltetrahydrofolate. J. Biol. Chem. 1998, 273:7873-7879.
-
(1998)
J. Biol. Chem.
, vol.273
, pp. 7873-7879
-
-
Zhao, R.1
Assaraf, Y.G.2
Goldman, I.D.3
-
70
-
-
34249671135
-
The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure
-
Zohn I.E., Anderson K.V., Niswander L. The Hectd1 ubiquitin ligase is required for development of the head mesenchyme and neural tube closure. Dev. Biol. 2007, 306:208-221.
-
(2007)
Dev. Biol.
, vol.306
, pp. 208-221
-
-
Zohn, I.E.1
Anderson, K.V.2
Niswander, L.3
-
71
-
-
58749113662
-
Modeling neural tube defects in the mouse
-
Zohn I.E., Sarkar A.A. Modeling neural tube defects in the mouse. Curr. Top. Dev. Biol. 2008, 84:1-35.
-
(2008)
Curr. Top. Dev. Biol.
, vol.84
, pp. 1-35
-
-
Zohn, I.E.1
Sarkar, A.A.2
|