-
2
-
-
0027265725
-
Prevalence of neural tube defects in South Australia, 1966-91: Effectiveness and impact of prenatal diagnosis
-
Chan A, Robertson EF, Haan EA, Keane RJ, Ranieri E, Carney A. Prevalence of neural tube defects in South Australia, 1966-91: effectiveness and impact of prenatal diagnosis. Br Med J 1993; 307:703-706.
-
(1993)
Br Med J
, vol.307
, pp. 703-706
-
-
Chan, A.1
Robertson, E.F.2
Haan, E.A.3
Keane, R.J.4
Ranieri, E.5
Carney, A.6
-
3
-
-
0028832419
-
Impact of prenatal diagnosis on the birth prevalence of neural tube defects, Atlanta, 1990-1991
-
Roberts HE, Moore CA, Cragan JD, Fernhoff PM, Khoury MJ. Impact of prenatal diagnosis on the birth prevalence of neural tube defects, Atlanta, 1990-1991. Pediatrics 1995; 96:880-883.
-
(1995)
Pediatrics
, vol.96
, pp. 880-883
-
-
Roberts, H.E.1
Moore, C.A.2
Cragan, J.D.3
Fernhoff, P.M.4
Khoury, M.J.5
-
4
-
-
0015767856
-
Epidemic waves in the prevalence of anencephaly and spina bifida in New York State
-
Janerich DT. Epidemic waves in the prevalence of anencephaly and spina bifida in New York State. Teratology 1973; 8:253-256.
-
(1973)
Teratology
, vol.8
, pp. 253-256
-
-
Janerich, D.T.1
-
5
-
-
0019847861
-
Apparent prevention of neural tube defects by periconceptional vitamin supplementation
-
Smithells RW, Sheppard S, Schorah CJ, Seller MJ, Nevin NC, Harris R, et al. Apparent prevention of neural tube defects by periconceptional vitamin supplementation. Arch Dis Child 1981; 56:911-918.
-
(1981)
Arch Dis Child
, vol.56
, pp. 911-918
-
-
Smithells, R.W.1
Sheppard, S.2
Schorah, C.J.3
Seller, M.J.4
Nevin, N.C.5
Harris, R.6
-
6
-
-
0025292327
-
The role of nutrition in neural tube defects
-
Scott JM, Kirke PN, Weir DG. The role of nutrition in neural tube defects. Annu Rev Nutr 1990; 10:277-295.
-
(1990)
Annu Rev Nutr
, vol.10
, pp. 277-295
-
-
Scott, J.M.1
Kirke, P.N.2
Weir, D.G.3
-
7
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
-
Wald N, Sneddon J, Densem J, Frost C, Stone R, MRC Vitamin Study Research Group. Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet 1991; 338:131-137.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
Wald, N.1
Sneddon, J.2
Densem, J.3
Frost, C.4
Stone, R.5
-
8
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation
-
Czeizel AE, Dudás 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
Dudás, I.2
-
9
-
-
0030998087
-
Knowledge about folic acid and the prevention of neural tube defects in two general practice populations
-
Krischer J. Knowledge about folic acid and the prevention of neural tube defects in two general practice populations. Br J Gen Pract 1997; 47:231-232. This questionnaire study shows a persisting lack of awareness, particularly among women in an inner-city area, of the link between folic acid supplementation and prevention of neural tube defects.
-
(1997)
Br J Gen Pract
, vol.47
, pp. 231-232
-
-
Krischer, J.1
-
10
-
-
0028021268
-
Minimal compliance with the Department of Health recommendation for routine folate prophylaxis to prevent fetal neural tube defects
-
Clark NAC, Fisk NM. Minimal compliance with the Department of Health recommendation for routine folate prophylaxis to prevent fetal neural tube defects. Br J Obstet Gynaecol 1994; 101:709-710.
-
(1994)
Br J Obstet Gynaecol
, vol.101
, pp. 709-710
-
-
Clark, N.A.C.1
Fisk, N.M.2
-
11
-
-
0029678181
-
Suboptimal compliance with periconceptual folic acid in an Irish hospital population
-
Milner M, Slevin J, Morrow A, Fawzy M, Clarke T, McKenna P. Suboptimal compliance with periconceptual folic acid in an Irish hospital population. Ir Med J 1996; 89:28-30.
-
(1996)
Ir Med J
, vol.89
, pp. 28-30
-
-
Milner, M.1
Slevin, J.2
Morrow, A.3
Fawzy, M.4
Clarke, T.5
McKenna, P.6
-
12
-
-
0029848516
-
How safe are folic acid supplements
-
Campbell NRC. How safe are folic acid supplements. Arch Intern Med 1996; 156:1638-1644.
-
(1996)
Arch Intern Med
, vol.156
, pp. 1638-1644
-
-
Campbell, N.R.C.1
-
13
-
-
0028247568
-
Folic acid metabolism and mechanisms of neural tube defects
-
Bock G, Marsh J (editors): Chichester: John Wiley & Sons;
-
Scott JM, Weir DG, Molloy A, McPartlin J, Daly L, Kirke P. Folic acid metabolism and mechanisms of neural tube defects. In: Bock G, Marsh J (editors): Neural tube defects (Ciba Foundation Symposium 181). Chichester: John Wiley & Sons; 1994. pp. 180-187.
-
(1994)
Neural Tube Defects (Ciba Foundation Symposium 181)
, pp. 180-187
-
-
Scott, J.M.1
Weir, D.G.2
Molloy, A.3
McPartlin, J.4
Daly, L.5
Kirke, P.6
-
14
-
-
0027198703
-
Absorption of pteroylpolyglutamates in mothers of infants with neural tube defects
-
Bower C, Stanley FJ, Croft M, De Klerk NH, Davis RE, Nicol DJ. Absorption of pteroylpolyglutamates in mothers of infants with neural tube defects. Br J Nutr 1993; 69:827-834.
-
(1993)
Br J Nutr
, vol.69
, pp. 827-834
-
-
Bower, C.1
Stanley, F.J.2
Croft, M.3
De Klerk, N.H.4
Davis, R.E.5
Nicol, D.J.6
-
16
-
-
0028833677
-
Homocysteine metabolism in pregnancies complicated by neural-tube defects
-
Mills JL, McPartlin JM, Kirke PN, Lee YJ, Conley MR, Weir DG, et al. Homocysteine metabolism in pregnancies complicated by neural-tube defects. Lancet 1995; 345:149-151.
-
(1995)
Lancet
, vol.345
, pp. 149-151
-
-
Mills, J.L.1
McPartlin, J.M.2
Kirke, P.N.3
Lee, Y.J.4
Conley, M.R.5
Weir, D.G.6
-
17
-
-
0030463010
-
Homocysteine induces congenital defects of the heart and neural tube: Effect of folic acid
-
Rosenquist TH, Ratashak SA, Selhub J. Homocysteine induces congenital defects of the heart and neural tube: effect of folic acid. Proc Natl Acad Sci USA 1996; 93:15227-15232.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 15227-15232
-
-
Rosenquist, T.H.1
Ratashak, S.A.2
Selhub, J.3
-
18
-
-
0028556581
-
Prevention of neural tube defects by and toxicity of L-homocysteine in cultured postimplantation rat embryos
-
VanAerts LAGJM, Blom HJ, Deabreu RA, Trijbels FJM, Eskes TKAB, Peereboom-Stegeman JHJC, et al. Prevention of neural tube defects by and toxicity of L-homocysteine in cultured postimplantation rat embryos. Teratology 1994; 50:348-360.
-
(1994)
Teratology
, vol.50
, pp. 348-360
-
-
VanAerts, L.A.G.J.M.1
Blom, H.J.2
Deabreu, R.A.3
Trijbels, F.J.M.4
Eskes, T.K.A.B.5
Peereboom-Stegeman, J.H.J.C.6
-
22
-
-
0030813123
-
Methionine synthase and neural tube defects
-
Morrison K, Edwards YH, Lynch SA, Burn J, Hol F, Mariman E. Methionine synthase and neural tube defects. J Med Genet 1997; 34:958.
-
(1997)
J Med Genet
, vol.34
, pp. 958
-
-
Morrison, K.1
Edwards, Y.H.2
Lynch, S.A.3
Burn, J.4
Hol, F.5
Mariman, E.6
-
23
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
Van der Put NMJ, Steegers-Theunissen RPM, Frosst P, Trijbels FJM, Eskes TKAB, Van den Heuvel LP, et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 1995; 346:1070-1071.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van Der Put, N.M.J.1
Steegers-Theunissen, R.P.M.2
Frosst, P.3
Trijbels, F.J.M.4
Eskes, T.K.A.B.5
Van Den Heuvel, L.P.6
-
24
-
-
0028803474
-
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL, Kirke PN, Burke H, Molloy AM, et al. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects. Q J Med 1995; 88:763-766.
-
(1995)
Q J Med
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
Kirke, P.N.4
Burke, H.5
Molloy, A.M.6
-
25
-
-
4143088796
-
Spina bifida, 677T → C mutation, and role of folate
-
De Franchis R, Sebastio G, Mandato C, Andria G, Mastroiacovo P. Spina bifida, 677T → C mutation, and role of folate. Lancet 1995; 346:1703.
-
(1995)
Lancet
, vol.346
, pp. 1703
-
-
De Franchis, R.1
Sebastio, G.2
Mandato, C.3
Andria, G.4
Mastroiacovo, P.5
-
26
-
-
0030034268
-
Relevance to spina bifida of mutated methylenetetrahydrofolate reductase
-
Wilcken DEL, Wang XL. Relevance to spina bifida of mutated methylenetetrahydrofolate reductase. Lancet 1996; 347:340.
-
(1996)
Lancet
, vol.347
, pp. 340
-
-
Wilcken, D.E.L.1
Wang, X.L.2
-
27
-
-
0029886679
-
Methylenetetrahydrofolate reductase and neural tube defects
-
Papapetrou C, Lynch SA, Burn J, Edwards YH. Methylenetetrahydrofolate reductase and neural tube defects. Lancet 1996; 348:58.
-
(1996)
Lancet
, vol.348
, pp. 58
-
-
Papapetrou, C.1
Lynch, S.A.2
Burn, J.3
Edwards, Y.H.4
-
28
-
-
0031066138
-
Is the common 677C → T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis
-
Van der Put NMJ, Eskes TKAB, Blom HJ. Is the common 677C → T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis. Q J Med 1997; 90:111-115. A meta-analysis of worldwide data on allele frequencies in the MTHFR gene support an association of the thermolabile allele with predisposition to neural tube defect.
-
(1997)
Q J Med
, vol.90
, pp. 111-115
-
-
Van Der Put, N.M.J.1
Eskes, T.K.A.B.2
Blom, H.J.3
-
29
-
-
0031044302
-
Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects?
-
Ramsbottom D, Scott JM, Molloy A, Weir DG, Kirke PN, Mills JL, et al. Are common mutations of cystathionine beta-synthase involved in the aetiology of neural tube defects? Clin Genet 1997; 51:39-42.
-
(1997)
Clin Genet
, vol.51
, pp. 39-42
-
-
Ramsbottom, D.1
Scott, J.M.2
Molloy, A.3
Weir, D.G.4
Kirke, P.N.5
Mills, J.L.6
-
30
-
-
0028244488
-
Multifactorial inheritance of neural tube defects: Localization of the major gene and recognition of modifiers in ct mutant mice
-
Neumann PE, Frankel WN, Letts VA, Coffin JM, Copp AJ, Bernfield M. Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant mice. Nature Genet 1994; 6:357-362.
-
(1994)
Nature Genet
, vol.6
, pp. 357-362
-
-
Neumann, P.E.1
Frankel, W.N.2
Letts, V.A.3
Coffin, J.M.4
Copp, A.J.5
Bernfield, M.6
-
31
-
-
0028856888
-
Mapping modifier genes for tail defects in curly-tail mutant mice
-
Letts VA, Schork NJ, Copp AJ, Bernfield M, Frankel WN. Mapping modifier genes for tail defects in curly-tail mutant mice. Genomics 1995; 29:719-724.
-
(1995)
Genomics
, vol.29
, pp. 719-724
-
-
Letts, V.A.1
Schork, N.J.2
Copp, A.J.3
Bernfield, M.4
Frankel, W.N.5
-
32
-
-
0028247567
-
Vitamins, folio acid and the cause and prevention of neural tube efects
-
Bock G, Marsh J (editors): Chichester: John Wiley & Sons;
-
Seller MJ. Vitamins, folio acid and the cause and prevention of neural tube efects. In: Bock G, Marsh J (editors): Neural tube defects (Ciba Foundation Symposium 181). Chichester: John Wiley & Sons; 1994. pp. 161-173.
-
(1994)
Neural Tube Defects (Ciba Foundation Symposium 181)
, pp. 161-173
-
-
Seller, M.J.1
-
33
-
-
0028847102
-
Dietary methionine does not reduce penetrance in curly tail mice but causes a phenotype-specific decrease in embryonic growth
-
Van Straaten HWM, Blom H, Peeters MCE, Rousseau AMJ, Cole KJ, Seller MJ. Dietary methionine does not reduce penetrance in curly tail mice but causes a phenotype-specific decrease in embryonic growth. J Nutr 1995; 125:2733-2740.
-
(1995)
J Nutr
, vol.125
, pp. 2733-2740
-
-
Van Straaten, H.W.M.1
Blom, H.2
Peeters, M.C.E.3
Rousseau, A.M.J.4
Cole, K.J.5
Seller, M.J.6
-
35
-
-
0031033593
-
Inositol prevents folate-resistant neural tube defects in the mouse
-
Greene NDE, Copp AJ. Inositol prevents folate-resistant neural tube defects in the mouse. Nature Med 1997; 3:60-66. Myo-inositol is demonstrated to prevent spinal defects in a mouse genetic model of folate-resistant neural tube defects.
-
(1997)
Nature Med
, vol.3
, pp. 60-66
-
-
Greene, N.D.E.1
Copp, A.J.2
-
36
-
-
0023681596
-
Changes with gestational age in the nutritional requirements of postimplantation rat embryos in culture
-
Cockroft DL. Changes with gestational age in the nutritional requirements of postimplantation rat embryos in culture. Teratology 1988; 38:281-290.
-
(1988)
Teratology
, vol.38
, pp. 281-290
-
-
Cockroft, D.L.1
-
37
-
-
0029946542
-
Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene
-
Zhao Q, Behringer RR, De Crombrugghe B. Prenatal folic acid treatment suppresses acrania and meroanencephaly in mice mutant for the Cart1 homeobox gene. Nature Genet 1996; 13:275-283.
-
(1996)
Nature Genet
, vol.13
, pp. 275-283
-
-
Zhao, Q.1
Behringer, R.R.2
De Crombrugghe, B.3
-
38
-
-
0027455468
-
Methionine but not folinic acid or vitamin B-12 alters the frequency of neural tube defects in Axdmutant mice
-
Essien FB, Wannberg SL. Methionine but not folinic acid or vitamin B-12 alters the frequency of neural tube defects in Axdmutant mice. J Nutr 1993; 123:27-34.
-
(1993)
J Nutr
, vol.123
, pp. 27-34
-
-
Essien, F.B.1
Wannberg, S.L.2
-
39
-
-
0029932086
-
Transcription factor AP-2 essential for cranial closure and craniofacial development
-
Schorle H, Meier P, Buchert M, Jaenisch R, Mitchell PJ. Transcription factor AP-2 essential for cranial closure and craniofacial development. Nature 1996; 381:235-238.
-
(1996)
Nature
, vol.381
, pp. 235-238
-
-
Schorle, H.1
Meier, P.2
Buchert, M.3
Jaenisch, R.4
Mitchell, P.J.5
-
40
-
-
0029932525
-
Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2
-
Zhang J, Hagopian-Donaldson S, Serbedzija G, Elsemore J, Plehn-Dujowich D, McMahon AP, et al. Neural tube, skeletal and body wall defects in mice lacking transcription factor AP-2. Nature 1996; 381:238-241.
-
(1996)
Nature
, vol.381
, pp. 238-241
-
-
Zhang, J.1
Hagopian-Donaldson, S.2
Serbedzija, G.3
Elsemore, J.4
Plehn-Dujowich, D.5
McMahon, A.P.6
-
41
-
-
0021472803
-
Pattern of serum protein gene expression in mouse visceral yolk sac and foetal liver
-
Meehan RR, Barlow DP, Hill RE, Hogan BLM, Hastie ND. Pattern of serum protein gene expression in mouse visceral yolk sac and foetal liver. EMBO J 1984; 3:1881-1885.
-
(1984)
EMBO J
, vol.3
, pp. 1881-1885
-
-
Meehan, R.R.1
Barlow, D.P.2
Hill, R.E.3
Hogan, B.L.M.4
Hastie, N.D.5
-
42
-
-
0027478167
-
Targeted modification of the apolipoprotein B gene results in hypobetalipoproteinemia and developmental abnormalities in mice
-
Homanics GE, Smith TJ, Zhang SH, Lee D, Young SG, Maeda N. Targeted modification of the apolipoprotein B gene results in hypobetalipoproteinemia and developmental abnormalities in mice. Proc Natl Acad Sci USA 1993; 90:2389-2393.
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 2389-2393
-
-
Homanics, G.E.1
Smith, T.J.2
Zhang, S.H.3
Lee, D.4
Young, S.G.5
Maeda, N.6
-
43
-
-
0025341313
-
Expression of a new mutation (Axd) causing axial defects in mice correlates with maternal phenotype and age
-
Essien FB, Haviland MB, Naidoff AE. Expression of a new mutation (Axd) causing axial defects in mice correlates with maternal phenotype and age. Teratology 1990; 42:183-194.
-
(1990)
Teratology
, vol.42
, pp. 183-194
-
-
Essien, F.B.1
Haviland, M.B.2
Naidoff, A.E.3
-
44
-
-
0017121568
-
The interfrontal bone and mutant genes in the mouse
-
Johnson DR. The interfrontal bone and mutant genes in the mouse. J Anat 1976; 121:507-513.
-
(1976)
J Anat
, vol.121
, pp. 507-513
-
-
Johnson, D.R.1
-
45
-
-
0030972376
-
Heart and neural tube defects in transgenic mice overexpressing the Cx43 gap junction gene
-
Ewart JL, Cohen MF, Meyer RA, Huang GY, Wessels A, Gourdie RG, et al. Heart and neural tube defects in transgenic mice overexpressing the Cx43 gap junction gene. Development 1997; 124:1281-1292.
-
(1997)
Development
, vol.124
, pp. 1281-1292
-
-
Ewart, J.L.1
Cohen, M.F.2
Meyer, R.A.3
Huang, G.Y.4
Wessels, A.5
Gourdie, R.G.6
-
46
-
-
0022227858
-
Experimental teratological studies with the mouse CNS mutations cranioschisis and delayed splotch
-
Kalter H. Experimental teratological studies with the mouse CNS mutations cranioschisis and delayed splotch. J Craniofac Genet Dev Biol 1985; (suppl 1):339-342.
-
(1985)
J Craniofac Genet Dev Biol
, Issue.1 SUPPL.
, pp. 339-342
-
-
Kalter, H.1
-
47
-
-
0001656609
-
A new crooked-tail mutation involving distinct pleiotropism
-
Morgan W. A new crooked-tail mutation involving distinct pleiotropism. J Genet 1954; 52:354-373.
-
(1954)
J Genet
, vol.52
, pp. 354-373
-
-
Morgan, W.1
-
48
-
-
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 1954; 52:52-67.
-
(1954)
J Genet
, vol.52
, pp. 52-67
-
-
Gruneberg, H.1
-
49
-
-
0018242811
-
Inheritance and morphology of exencephaly, a neonatal recessive with partial penetrance, in the house mouse
-
Wallace ME, Knights PJ, Anderson JR. Inheritance and morphology of exencephaly, a neonatal recessive with partial penetrance, in the house mouse. Genet Res 1978; 32:135-149.
-
(1978)
Genet Res
, vol.32
, pp. 135-149
-
-
Wallace, M.E.1
Knights, P.J.2
Anderson, J.R.3
-
50
-
-
0026445646
-
Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt)
-
Schimmang T, Lemaistre M, Vortkamp A, Rüther U. Expression of the zinc finger gene Gli3 is affected in the morphogenetic mouse mutant extra-toes (Xt). Development 1992; 116:799-804.
-
(1992)
Development
, vol.116
, pp. 799-804
-
-
Schimmang, T.1
Lemaistre, M.2
Vortkamp, A.3
Rüther, U.4
-
51
-
-
0027478216
-
J mutation contains an intragenic deletion of the Gli3 gene
-
J mutation contains an intragenic deletion of the Gli3 gene. Nature Genet 1993; 3:241-246.
-
(1993)
Nature Genet
, vol.3
, pp. 241-246
-
-
Hui, C.1
Joyner, A.L.2
-
52
-
-
0031149883
-
Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development
-
Deng CX, Bedford M, Li CL, Xu XL, Yang X, Dunmore J, et al. Fibroblast growth factor receptor-1 (FGFR-1) is essential for normal neural tube and limb development. Dev Biol 1997; 185:42-54.
-
(1997)
Dev Biol
, vol.185
, pp. 42-54
-
-
Deng, C.X.1
Bedford, M.2
Li, C.L.3
Xu, X.L.4
Yang, X.5
Dunmore, J.6
-
53
-
-
0029188455
-
Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects
-
Ishibashi M, Ang S-L, Shiota K, Nakanishi S, Kageyama R, Guillemot F. Targeted disruption of mammalian hairy and Enhancer of split homolog-1 (HES-1) leads to up-regulation of neural helix-loop-helix factors, premature neurogenesis, and severe neural tube defects. Genes Dev 1995; 9:3136-3148.
-
(1995)
Genes Dev
, vol.9
, pp. 3136-3148
-
-
Ishibashi, M.1
Ang, S.-L.2
Shiota, K.3
Nakanishi, S.4
Kageyama, R.5
Guillemot, F.6
-
54
-
-
0025864268
-
Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression
-
Lufkin T, Dierich A, LeMeur M, Mark M, Chambon P. Disruption of the Hox-1.6 homeobox gene results in defects in a region corresponding to its rostral domain of expression. Cell 1991; 66:1105-1119.
-
(1991)
Cell
, vol.66
, pp. 1105-1119
-
-
Lufkin, T.1
Dierich, A.2
Lemeur, M.3
Mark, M.4
Chambon, P.5
-
55
-
-
0029004775
-
Gene trap capture of a novel mouse gene, jumonji, required for neural tube formation
-
Takeuchi T, Yamazaki Y, Katoh-Fukui Y, Tsuchiya R, Kondo S, Motoyama J, Higashinakagawa T. Gene trap capture of a novel mouse gene, jumonji, required for neural tube formation. Genes Dev 1995; 9:1211-1222.
-
(1995)
Genes Dev
, vol.9
, pp. 1211-1222
-
-
Takeuchi, T.1
Yamazaki, Y.2
Katoh-Fukui, Y.3
Tsuchiya, R.4
Kondo, S.5
Motoyama, J.6
Higashinakagawa, T.7
-
56
-
-
0001511418
-
Hereditary loop-tail in the house mouse
-
Strong LC, Hollander WF. Hereditary loop-tail in the house mouse. J Hered 1949; 40:329-334.
-
(1949)
J Hered
, vol.40
, pp. 329-334
-
-
Strong, L.C.1
Hollander, W.F.2
-
57
-
-
0028988719
-
Genetic basis of neural tube defects: The mouse gene loop-tail maps to a region of Chromosome 1 syntenic with human 1q21-22
-
Stanier P, Henson JN, Eddleston J, Moore GE, Copp AJ. Genetic basis of neural tube defects: the mouse gene loop-tail maps to a region of Chromosome 1 syntenic with human 1q21-22. Genomics 1995; 26:473-478.
-
(1995)
Genomics
, vol.26
, pp. 473-478
-
-
Stanier, P.1
Henson, J.N.2
Eddleston, J.3
Moore, G.E.4
Copp, A.J.5
-
59
-
-
9044254925
-
Neural tube defects and abnormal brain development in F52-deficient mice
-
Wu M, Chen DF, Sasaoka T, Tonegawa S. Neural tube defects and abnormal brain development in F52-deficient mice. Proc Natl Acad Sci USA 1996; 93:2110-2115.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 2110-2115
-
-
Wu, M.1
Chen, D.F.2
Sasaoka, T.3
Tonegawa, S.4
-
60
-
-
0029957831
-
Disruption of the MacMARCKS gene prevents cranial neural tube closure and results in anencephaly
-
Chen J, Chang S, Duncan SA, Okano HJ, Fishell G, Aderem A. Disruption of the MacMARCKS gene prevents cranial neural tube closure and results in anencephaly. Proc Natl Acad Sci USA 1996; 93:6275-6279.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 6275-6279
-
-
Chen, J.1
Chang, S.2
Duncan, S.A.3
Okano, H.J.4
Fishell, G.5
Aderem, A.6
-
61
-
-
0028089937
-
Open brain, a new mouse mutant with severe neural tube defects, shows altered gene expression patterns in the developing spinal cord
-
Günther T, Struwe M, Aguzzi A, Schughart K. Open brain, a new mouse mutant with severe neural tube defects, shows altered gene expression patterns in the developing spinal cord. Development 1994; 120:3119-3130.
-
(1994)
Development
, vol.120
, pp. 3119-3130
-
-
Günther, T.1
Struwe, M.2
Aguzzi, A.3
Schughart, K.4
-
63
-
-
0029007405
-
A subset of p53-deficient embryos exhibit exencephaly
-
Sah VP, Attardi LD, Mulligan GJ, Williams BO, Bronson RT, Jacks T. A subset of p53-deficient embryos exhibit exencephaly. Nature Genet 1995; 10:175-180.
-
(1995)
Nature Genet
, vol.10
, pp. 175-180
-
-
Sah, V.P.1
Attardi, L.D.2
Mulligan, G.J.3
Williams, B.O.4
Bronson, R.T.5
Jacks, T.6
-
64
-
-
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, Schatteman GC, Bork T, Bowen-Pope DF, Weston JA. A PDGF receptor mutation in the mouse (Patch) perturbs the development of a non-neuronal subset of neural crest-derived cells. Development 1992; 115:133-142.
-
(1992)
Development
, vol.115
, pp. 133-142
-
-
Morrison-Graham, K.1
Schatteman, G.C.2
Bork, T.3
Bowen-Pope, D.F.4
Weston, J.A.5
-
65
-
-
0026695298
-
Developmental expression of the a receptor for platelet-derived growth factor, which is deleted in the embryonic lethal Patch mutation
-
Orr-Urtreger A, Bedford MT, Do M-S, Eisenbach L, Lonai P. Developmental expression of the a receptor for platelet-derived growth factor, which is deleted in the embryonic lethal Patch mutation. Development 1992; 115:289-303.
-
(1992)
Development
, vol.115
, pp. 289-303
-
-
Orr-Urtreger, A.1
Bedford, M.T.2
Do, M.-S.3
Eisenbach, L.4
Lonai, P.5
-
66
-
-
0028971681
-
Disruption of the mouse RBP-Jkappa gene results in early embryonic death
-
Oka C, Nakano T, Wakeham A, De la Pompa JL, Mori C, Sakai T, et al. Disruption of the mouse RBP-Jkappa gene results in early embryonic death. Development 1995; 121:3291-3301.
-
(1995)
Development
, vol.121
, pp. 3291-3301
-
-
Oka, C.1
Nakano, T.2
Wakeham, A.3
De La Pompa, J.L.4
Mori, C.5
Sakai, T.6
-
67
-
-
0028088752
-
Function of the retinoic acid receptors (RARs) during development. (I) Craniofacial and skeletal abnormalities in RAR double mutants
-
Lohnes D, Mark M, Mendelsohn C, Dolle P, Dierich A, Gorry P, et al. Function of the retinoic acid receptors (RARs) during development. (I) Craniofacial and skeletal abnormalities in RAR double mutants. Development 1994; 120:2723-2748.
-
(1994)
Development
, vol.120
, pp. 2723-2748
-
-
Lohnes, D.1
Mark, M.2
Mendelsohn, C.3
Dolle, P.4
Dierich, A.5
Gorry, P.6
-
68
-
-
0009625158
-
The development of rib fusions, a mutation in the house mouse
-
Theiler K, Stevens LC. The development of rib fusions, a mutation in the house mouse. Am J Anat 1960; 106:171-183.
-
(1960)
Am J Anat
, vol.106
, pp. 171-183
-
-
Theiler, K.1
Stevens, L.C.2
-
69
-
-
0024422922
-
Genetic analysis of the cause of exencephaly in the SELH/Bc mouse stock
-
Juriloff DM, MacDonald KB, Harris MJ. Genetic analysis of the cause of exencephaly in the SELH/Bc mouse stock. Teratology 1989; 40:395-405.
-
(1989)
Teratology
, vol.40
, pp. 395-405
-
-
Juriloff, D.M.1
MacDonald, K.B.2
Harris, M.J.3
-
70
-
-
0025875226
-
Pax-3, a novel murine DNA binding protein expressed during early neurogenesis
-
Goulding MD, Chalepakis G, Deutsch U, Erselius JR, Gruss P. Pax-3, a novel murine DNA binding protein expressed during early neurogenesis. EMBO J 1991; 10:1135-1147.
-
(1991)
EMBO J
, vol.10
, pp. 1135-1147
-
-
Goulding, M.D.1
Chalepakis, G.2
Deutsch, U.3
Erselius, J.R.4
Gruss, P.5
-
71
-
-
0025925068
-
2H). A mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3
-
2H). a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3. Cell 1991; 67:767-774.
-
(1991)
Cell
, vol.67
, pp. 767-774
-
-
Epstein, D.J.1
Vekemans, M.2
Gros, P.3
-
72
-
-
0028933142
-
Twist is required in head mesenchyme for cranial neural tube morphogenesis
-
Chen Z-F, Behringer RR. 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
-
73
-
-
0022629758
-
Pathogenesis of neural dysraphism in the mouse mutant vacuolated lens (vI)
-
Wilson DB, Wyatt DP. Pathogenesis of neural dysraphism in the mouse mutant vacuolated lens (vI). J Neuropathol Exp Neurol 1986; 45:43-55.
-
(1986)
J Neuropathol Exp Neurol
, vol.45
, pp. 43-55
-
-
Wilson, D.B.1
Wyatt, D.P.2
-
74
-
-
0027323660
-
Interaction between splotch (Sp) and curly tail (ct) mouse mutants in the embryonic development of neural tube defects
-
Estibeiro JP, Brook FA, Copp AJ. Interaction between splotch (Sp) and curly tail (ct) mouse mutants in the embryonic development of neural tube defects. Development 1993; 119:113-121.
-
(1993)
Development
, vol.119
, pp. 113-121
-
-
Estibeiro, J.P.1
Brook, F.A.2
Copp, A.J.3
|