-
1
-
-
84874365790
-
The continuing challenge of understanding, preventing, and treating neural tube defects
-
PMID:23449594
-
Wallingford JB, Niswander LA, Shaw GM, Finnell RH. The continuing challenge of understanding, preventing, and treating neural tube defects. Science 2013; 339:1222002; PMID:23449594; http://dx.doi.org/10.1126/science.1222002
-
(2013)
Science
, vol.339
-
-
Wallingford, J.B.1
Niswander, L.A.2
Shaw, G.M.3
Finnell, R.H.4
-
2
-
-
84880329695
-
-
Lancet Neurol, PMID:23790957
-
Copp AJ, Stanier P, Greene ND. Neural tube defects: recent advances, unsolved questions, and controversies. Lancet Neurol 2013; PMID:23790957
-
(2013)
Neural Tube Defects: Recent Advances, Unsolved Questions, and Controversies
-
-
Copp, A.J.1
Stanier, P.2
Greene, N.D.3
-
3
-
-
77951653496
-
Epidemiologic and genetic aspects of spina bifida and other neural tube defects
-
PMID:20419766
-
Au KS, Ashley-Koch A, Northrup H. Epidemiologic and genetic aspects of spina bifida and other neural tube defects. Dev Disabil Res Rev 2010; 16:6-15; PMID:20419766; http://dx.doi.org/10.1002/ddrr.93
-
(2010)
Dev Disabil Res Rev
, vol.16
, pp. 6-15
-
-
Au, K.S.1
Ashley-Koch, A.2
Northrup, H.3
-
4
-
-
33947172588
-
Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects
-
PMID:17177317
-
Harris MJ, Juriloff DM. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects. Birth Defects Res A Clin Mol Teratol 2007; 79:187-210; PMID:17177317; http://dx.doi.org/10.1002/bdra.20333
-
(2007)
Birth Defects Res a Clin Mol Teratol
, vol.79
, pp. 187-210
-
-
Harris, M.J.1
Juriloff, D.M.2
-
5
-
-
77955649698
-
An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure
-
PMID:20740593
-
Harris MJ, Juriloff DM. An update to the list of mouse mutants with neural tube closure defects and advances toward a complete genetic perspective of neural tube closure. Birth Defects Res A Clin Mol Teratol 2010; 88:653-69; PMID:20740593; http://dx.doi.org/10.1002/bdra.20676
-
(2010)
Birth Defects Res a Clin Mol Teratol
, vol.88
, pp. 653-669
-
-
Harris, M.J.1
Juriloff, D.M.2
-
6
-
-
33747588534
-
Neural tube defects and folate: Case far from closed
-
PMID:16924261
-
Blom HJ, Shaw GM, den Heijer M, Finnell RH. Neural tube defects and folate: case far from closed. Nat Rev Neurosci 2006; 7:724-31; PMID:16924261; http://dx.doi.org/10.1038/nrn1986
-
(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
-
7
-
-
0027145847
-
Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects
-
PMID:8265769
-
Kirke PN, Molloy AM, Daly LE, Burke H, Weir DG, Scott JM. Maternal plasma folate and vitamin B12 are independent risk factors for neural tube defects. QJ Med 1993; 86:703-8; PMID:8265769
-
(1993)
QJ Med
, vol.86
, pp. 703-708
-
-
Kirke, P.N.1
Molloy, A.M.2
Daly, L.E.3
Burke, H.4
Weir, D.G.5
Scott, J.M.6
-
8
-
-
17544402720
-
Inositol and folate resistant neural tube defects
-
PMID:11836374
-
Cavalli P, Copp AJ. Inositol and folate resistant neural tube defects. J Med Gen 2002; 39: 5; PMID:11836374
-
(2002)
J Med Gen
, vol.39
, pp. 5
-
-
Cavalli, P.1
Copp, A.J.2
-
9
-
-
77954755253
-
Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study
-
PMID:20641100
-
Chen X, Guo J, Lei Y, Zou J, Lu X, Bao Y, Wu L, Wu J, Zheng X, Shen Y, et al. Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study. Birth Defects Res A Clin Mol Teratol 2010; 88:575-81; PMID:20641100; http://dx.doi.org/10.1002/bdra.20670
-
(2010)
Birth Defects Res a Clin Mol Teratol
, vol.88
, pp. 575-581
-
-
Chen, X.1
Guo, J.2
Lei, Y.3
Zou, J.4
Lu, X.5
Bao, Y.6
Wu, L.7
Wu, J.8
Zheng, X.9
Shen, Y.10
-
10
-
-
0037117501
-
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status
-
PMID:11929966
-
Friso S, Choi SW, Girelli D, Mason JB, Dolnikowski GG, Bagley PJ, Olivieri O, Jacques PF, Rosenberg IH, Corrocher R, et al. A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. Proc Nat Acad Sci U S A 2002; 99:5606-11; PMID:11929966
-
(2002)
Proc Nat Acad Sci U S A
, vol.99
, pp. 5606-5611
-
-
Friso, S.1
Choi, S.W.2
Girelli, D.3
Mason, J.B.4
Dolnikowski, G.G.5
Bagley, P.J.6
Olivieri, O.7
Jacques, P.F.8
Rosenberg, I.H.9
Corrocher, R.10
-
11
-
-
77951949256
-
Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects
-
PMID:20164316
-
Wang L, Wang F, Guan J, Le J, Wu L, Zou J, Zhao H, Pei L, Zheng X, Zhang T. Relation between hypomethylation of long interspersed nucleotide elements and risk of neural tube defects. Am J Clin Nutrit 2010; 91:1359-67; PMID:20164316; http://dx.doi.org/10.3945/ajcn.2009.28858
-
(2010)
Am J Clin Nutrit
, vol.91
, pp. 1359-1367
-
-
Wang, L.1
Wang, F.2
Guan, J.3
Le, J.4
Wu, L.5
Zou, J.6
Zhao, H.7
Pei, L.8
Zheng, X.9
Zhang, T.10
-
12
-
-
79960141859
-
Tissue-specific distribution of aberrant DNA methylation associated with maternal low-folate status in human neural tube defects
-
PMID:21333513
-
Chang H, Zhang T, Zhang Z, Bao R, Fu C, Wang Z, Bao Y, Li Y, Wu L, Zheng X, et al. Tissue-specific distribution of aberrant DNA methylation associated with maternal low-folate status in human neural tube defects. J Nutrit Biochem 2011; 22:1172-7; PMID:21333513; http://dx.doi.org/10.1016/j.jnutbio.2010.10.003
-
(2011)
J Nutrit Biochem
, vol.22
, pp. 1172-1177
-
-
Chang, H.1
Zhang, T.2
Zhang, Z.3
Bao, R.4
Fu, C.5
Wang, Z.6
Bao, Y.7
Li, Y.8
Wu, L.9
Zheng, X.10
-
13
-
-
79960124420
-
The emerging role of epigenetic mechanisms in the aetiology of neural tube defects
-
PMID:21613818
-
Greene NDE, Stanier P, Moore GE. The emerging role of epigenetic mechanisms in the aetiology of neural tube defects. Epigenetics 2011; 6:875-83; PMID:21613818; http://dx.doi.org/10.4161/epi.6.7.16400
-
(2011)
Epigenetics
, vol.6
, pp. 875-883
-
-
Greene, N.1
Stanier, P.2
Moore, G.E.3
-
14
-
-
77649267695
-
Dynamic changes in the human methylome during differentiation
-
PMID:20133333
-
Laurent L, Wong E, Li G, Huynh T, Tsirigos A, Ong CT, Low HM, Kin Sung KW, Rigoutsos I, Loring J, et al. Dynamic changes in the human methylome during differentiation. Genome research 2010; 20:320-31; PMID:20133333; http://dx.doi.org/10.1101/gr.101907.109
-
(2010)
Genome Research
, vol.20
, pp. 320-331
-
-
Laurent, L.1
Wong, E.2
Li, G.3
Huynh, T.4
Tsirigos, A.5
Ong, C.T.6
Low, H.M.7
Kin Sung, K.W.8
Rigoutsos, I.9
Loring, J.10
-
15
-
-
0036644303
-
Testing for genetic associations in a spina bifida population: Analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects
-
PMID:12116226
-
Volcik KA, Blanton SH, Kruzel MC, Townsend IT, Tyerman GH, Mier RJ, Northrup H. Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects. A J Med Genet 2002; 110:203-7; PMID:12116226; http://dx.doi.org/10.1002/ajmg.10435
-
(2002)
A J Med Genet
, vol.110
, pp. 203-207
-
-
Volcik, K.A.1
Blanton, S.H.2
Kruzel, M.C.3
Townsend, I.T.4
Tyerman, G.H.5
Mier, R.J.6
Northrup, H.7
-
16
-
-
0036966642
-
Hox genes and spinal cord development
-
PMID:12145408
-
Carpenter EM. Hox genes and spinal cord development. Dev Neurosci 2002; 24:24-34; PMID:12145408
-
(2002)
Dev Neurosci
, vol.24
, pp. 24-34
-
-
Carpenter, E.M.1
-
17
-
-
77956616754
-
Epigenetic control of Hox genes during neurogenesis, development, and disease
-
PMID:20739155
-
Barber BA, Rastegar M. Epigenetic control of Hox genes during neurogenesis, development, and disease. Ann Anat 2010; 192:261-74; PMID:20739155
-
(2010)
Ann Anat
, vol.192
, pp. 261-274
-
-
Barber, B.A.1
Rastegar, M.2
-
18
-
-
2442695407
-
Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription
-
PMID:15155579
-
Chambeyron S, Bickmore WA. Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription. GenDev 2004; 18:1119-30; PMID:15155579; http://dx.doi.org/10.1101/gad.292104
-
(2004)
Gendev
, vol.18
, pp. 1119-1130
-
-
Chambeyron, S.1
Bickmore, W.A.2
-
19
-
-
84876785540
-
The histone deacetylase inhibitor sodium valproate causes limited transcriptional change in mouse embryonic stem cells but selectively overrides Polycomb-mediated Hoxb silencing
-
PMID:23634885
-
Boudadi E, Stower H, Halsall JA, Rutledge CE, Leeb M, Wutz A, O’Neill LP, Nightingale KP, Turner BM. The histone deacetylase inhibitor sodium valproate causes limited transcriptional change in mouse embryonic stem cells but selectively overrides Polycomb-mediated Hoxb silencing. Epigenet Chromat 2013; 6:11; PMID:23634885; http://dx.doi.org/10.1186/1756-8935-6-11
-
(2013)
Epigenet Chromat
, vol.6
, pp. 11
-
-
Boudadi, E.1
Stower, H.2
Halsall, J.A.3
Rutledge, C.E.4
Leeb, M.5
Wutz, A.6
O’Neill, L.P.7
Nightingale, K.P.8
Turner, B.M.9
-
20
-
-
0031887992
-
Zebrafish hox genes: Genomic organization and modified collinear expression patterns in the trunk
-
PMID:9425136
-
Prince VE, Joly L, Ekker M, Ho RK. Zebrafish hox genes: genomic organization and modified collinear expression patterns in the trunk. Development 1998; 125:407-20; PMID:9425136
-
(1998)
Development
, vol.125
, pp. 407-420
-
-
Prince, V.E.1
Joly, L.2
Ekker, M.3
Ho, R.K.4
-
21
-
-
0036382945
-
The hox paradox: More complex(es) than imagined
-
PMID:12217314
-
Prince V. The hox paradox: more complex(es) than imagined. Dev Bio 2002; 249:1-15; PMID:12217314; http://dx.doi.org/10.1006/dbio.2002.0745
-
(2002)
Dev Bio
, vol.249
, pp. 1-15
-
-
Prince, V.1
-
22
-
-
84884733707
-
Hox genes: Choreographers in neural development, architects of circuit organization
-
PMID:24094100
-
Philippidou P, Dasen JS. Hox genes: choreographers in neural development, architects of circuit organization. Neuron 2013; 80:12-34; PMID:24094100; http://dx.doi.org/10.1016/j.neuron.2013.09.020
-
(2013)
Neuron
, vol.80
, pp. 12-34
-
-
Philippidou, P.1
Dasen, J.S.2
-
23
-
-
84877924809
-
Duplications of hox gene clusters and the emergence of vertebrates
-
PMID:23501471
-
Soshnikova N, Dewaele R, Janvier P, Krumlauf R, Duboule D. Duplications of hox gene clusters and the emergence of vertebrates. Dev Biol 2013; 378:194-9; PMID:23501471; http://dx.doi.org/10.1016/j.ydbio.2013.03.004
-
(2013)
Dev Biol
, vol.378
, pp. 194-199
-
-
Soshnikova, N.1
Dewaele, R.2
Janvier, P.3
Krumlauf, R.4
Duboule, D.5
-
24
-
-
84884418515
-
Combined function of HoxA and HoxB clusters in neural crest cells
-
PMID:23850771
-
Vieux-Rochas M, Mascrez B, Krumlauf R, Duboule D. Combined function of HoxA and HoxB clusters in neural crest cells. Dev Biol 2013; 382:293-301; PMID:23850771; http://dx.doi.org/10.1016/j.ydbio.2013.06.027
-
(2013)
Dev Biol
, vol.382
, pp. 293-301
-
-
Vieux-Rochas, M.1
Mascrez, B.2
Krumlauf, R.3
Duboule, D.4
-
25
-
-
0034303585
-
Neuronal specification in the spinal cord: Inductive signals and transcriptional codes
-
PMID:11262869
-
Jessell TM. Neuronal specification in the spinal cord: inductive signals and transcriptional codes. Nat Rev Genet 2000; 1:20-9; PMID:11262869; http://dx.doi.org/10.1038/35049541
-
(2000)
Nat Rev Genet
, vol.1
, pp. 20-29
-
-
Jessell, T.M.1
-
26
-
-
0029588307
-
As an inducer of anteroposterior neural pattern
-
PMID:8548794
-
Doniach T. Basic FGF as an inducer of anteroposterior neural pattern. Cell 1995; 83:1067-70; PMID:8548794
-
(1995)
Cell
, vol.83
, pp. 1067-1070
-
-
Doniach, T.1
Basic, F.2
-
27
-
-
77953615172
-
VANGL1 rare variants associated with neural tube defects affect convergent extension in zebrafish
-
PMID:20043994
-
Reynolds A, McDearmid JR, Lachance S, De Marco P, Merello E, Capra V, Gros P, Drapeau P, Kibar Z. VANGL1 rare variants associated with neural tube defects affect convergent extension in zebrafish. Mech Dev 2010; 127:385-92; PMID:20043994; http://dx.doi.org/10.1016/j.mod.2009.12.002
-
(2010)
Mech Dev
, vol.127
, pp. 385-392
-
-
Reynolds, A.1
McDearmid, J.R.2
Lachance, S.3
De Marco, P.4
Merello, E.5
Capra, V.6
Gros, P.7
Drapeau, P.8
Kibar, Z.9
-
28
-
-
84884920554
-
Distinctive patterns of DNA methylation associated with Parkinson disease: Identification of concordant epigenetic changes in brain and peripheral blood leukocytes
-
PMID:23907097
-
Masliah E, Dumaop W, Galasko D, Desplats P. Distinctive patterns of DNA methylation associated with Parkinson disease: identification of concordant epigenetic changes in brain and peripheral blood leukocytes. Epigenetics 2013; 8:1030-8; PMID:23907097; http://dx.doi.org/10.4161/epi.25865
-
(2013)
Epigenetics
, vol.8
, pp. 1030-1038
-
-
Masliah, E.1
Dumaop, W.2
Galasko, D.3
Desplats, P.4
-
29
-
-
84885705541
-
On the outside, looking in: A review and evaluation of the comparability of blood and brain "-omes"
-
PMID:24132893
-
Tylee DS, Kawaguchi DM, Glatt SJ. On the outside, looking in: a review and evaluation of the comparability of blood and brain "-omes". Am J Med Genet B Neuropsychiatr Genet 2013; 162B:595-603; PMID:24132893
-
Am J Med Genet B Neuropsychiatr Genet 2013
, vol.162
, pp. 595-603
-
-
Tylee, D.S.1
Kawaguchi, D.M.2
Glatt, S.J.3
-
30
-
-
84880867623
-
DNA methylation of the BDNF gene and its relevance to psychiatric disorders
-
PMID:23739121
-
Ikegame T, Bundo M, Murata Y, Kasai K, Kato T, Iwamoto K. DNA methylation of the BDNF gene and its relevance to psychiatric disorders. J Hum Genet 2013; 58:434-8; PMID:23739121; http://dx.doi.org/10.1038/jhg.2013.65
-
(2013)
J Hum Genet
, vol.58
, pp. 434-438
-
-
Ikegame, T.1
Bundo, M.2
Murata, Y.3
Kasai, K.4
Kato, T.5
Iwamoto, K.6
-
31
-
-
77449087922
-
A similar cell-specific pattern of HOXA methylation in normal and in cancer tissues
-
PMID:20083893
-
Avraham A, Sandbank J, Yarom N, Shalom A, Karni T, Pappo I, Sella A, Fich A, Walfisch S, Gheber L, et al. A similar cell-specific pattern of HOXA methylation in normal and in cancer tissues. Epigenetics 2010; 5:41-6; PMID:20083893; http://dx.doi.org/10.4161/epi.5.1.10724
-
(2010)
Epigenetics
, vol.5
, pp. 41-46
-
-
Avraham, A.1
Sandbank, J.2
Yarom, N.3
Shalom, A.4
Karni, T.5
Pappo, I.6
Sella, A.7
Fich, A.8
Walfisch, S.9
Gheber, L.10
-
32
-
-
80053304450
-
High density DNA methylation array with single CpG site resolution
-
PMID:21839163
-
Bibikova M, Barnes B, Tsan C, Ho V, Klotzle B, Le JM, Delano D, Zhang L, Schroth GP, Gunderson KL, et al. High density DNA methylation array with single CpG site resolution. Genomics 2011; 98:288-95; PMID:21839163; http://dx.doi.org/10.1016/j.ygeno.2011.07.007
-
(2011)
Genomics
, vol.98
, pp. 288-295
-
-
Bibikova, M.1
Barnes, B.2
Tsan, C.3
Ho, V.4
Klotzle, B.5
Le, J.M.6
Delano, D.7
Zhang, L.8
Schroth, G.P.9
Gunderson, K.L.10
-
33
-
-
84893852621
-
-
Brief Bioinformat, PMID:23990268
-
Dedeurwaerder S, Defrance M, Bizet M, Calonne E, Bontempi G, Fuks F. A comprehensive overview of Infinium HumanMethylation450 data processing. Brief Bioinformat 2013; PMID:23990268; http://dx.doi.org/10.1093/bib/bbt054
-
(2013)
A Comprehensive Overview of Infinium Humanmethylation450 Data Processing
-
-
Dedeurwaerder, S.1
Defrance, M.2
Bizet, M.3
Calonne, E.4
Bontempi, G.5
Fuks, F.6
-
34
-
-
84863230488
-
IMA: An R package for high-throughput analysis of Illumina’s 450K Infinium methylation data
-
PMID:22253290
-
Wang D, Yan L, Hu Q, Sucheston LE, Higgins MJ, Ambrosone CB, Johnson CS, Smiraglia DJ, Liu S. IMA: an R package for high-throughput analysis of Illumina’s 450K Infinium methylation data. Bioinformatics 2012; 28:729-30; PMID:22253290; http://dx.doi.org/10.1093/bioinformatics/bts013
-
(2012)
Bioinformatics
, vol.28
, pp. 729-730
-
-
Wang, D.1
Yan, L.2
Hu, Q.3
Sucheston, L.E.4
Higgins, M.J.5
Ambrosone, C.B.6
Johnson, C.S.7
Smiraglia, D.J.8
Liu, S.9
-
35
-
-
77957753745
-
A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system
-
PMID:20807523
-
Izzi B, Decallonne B, Devriendt K, Bouillon R, Vanderschueren D, Levtchenko E, de Zegher F, Van den Bruel A, Lambrechts D, Van Geet C, et al. A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system. Clin Chim Acta 2010; 411:2033-9; PMID:20807523; http://dx.doi.org/10.1016/j.cca.2010.08.034
-
(2010)
Clin Chim Acta
, vol.411
, pp. 2033-2039
-
-
Izzi, B.1
Decallonne, B.2
Devriendt, K.3
Bouillon, R.4
Vanderschueren, D.5
Levtchenko, E.6
De Zegher, F.7
Van Den Bruel, A.8
Lambrechts, D.9
Van Geet, C.10
-
36
-
-
84861839425
-
Methylation defect in imprinted genes detected in patients with an Albright’s hereditary osteodystrophy like phenotype and platelet Gs hypofunction
-
PMID:22679513;
-
Izzi B, Francois I, Labarque V, Thys C, Wittevrongel C, Devriendt K, Legius E, Van den Bruel A, D’Hooghe M, Lambrechts D, et al. Methylation defect in imprinted genes detected in patients with an Albright’s hereditary osteodystrophy like phenotype and platelet Gs hypofunction. PloS one 2012; 7:e38579; PMID:22679513;http://dx.doi.org/10.1371/journal.pone.0038579
-
(2012)
Plos One
, vol.38579
, pp. 7
-
-
Izzi, B.1
Francois, I.2
Labarque, V.3
Thys, C.4
Wittevrongel, C.5
Devriendt, K.6
Legius, E.7
Van Den Bruel, A.8
D’Hooghe, M.9
Lambrechts, D.10
-
37
-
-
84924419856
-
Pyrosequencing evaluation of widely available bisulfite conversion methods: Considerations for application
-
PMID:24944560
-
Izzi B, Binder AM, Michels KB. Pyrosequencing evaluation of widely available bisulfite conversion methods: considerations for application. Med Epigenet 2014; 2:28-36; PMID:24944560
-
(2014)
Med Epigenet
, vol.2
, pp. 28-36
-
-
Izzi, B.1
Binder, A.M.2
Michels, K.B.3
-
38
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
PMID:7647779
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, Boers GJ, den Heijer M, Kluijtmans LA, van den Heuvel LP, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10:111-3; PMID:7647779; http://dx.doi.org/10.1038/ng0595-111
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
Boers, G.J.7
Den Heijer, M.8
Kluijtmans, L.A.9
Van Den Heuvel, L.P.10
-
39
-
-
84875376002
-
MENT: Methylation and expression database of normal and tumor tissues
-
PMID:23219992
-
Baek SJ, Yang S, Kang TW, Park SM, Kim YS, Kim SY. MENT: methylation and expression database of normal and tumor tissues. Gene 2013; 518:194-200; PMID:23219992; http://dx.doi.org/10.1016/j.gene.2012.11.032
-
(2013)
Gene
, vol.518
, pp. 194-200
-
-
Baek, S.J.1
Yang, S.2
Kang, T.W.3
Park, S.M.4
Kim, Y.S.5
Kim, S.Y.6
-
41
-
-
0029045033
-
Stages of embryonic development of the zebrafish
-
PMID:8589427
-
Kimmel CB, Ballard WW, Kimmel SR, Ullmann B, Schilling TF. Stages of embryonic development of the zebrafish. Dev Dyn 1995; 203:253-310; PMID:8589427; http://dx.doi.org/10.1002/aja.1002030302
-
(1995)
Dev Dyn
, vol.203
, pp. 253-310
-
-
Kimmel, C.B.1
Ballard, W.W.2
Kimmel, S.R.3
Ullmann, B.4
Schilling, T.F.5
-
42
-
-
0025992094
-
Zebrafish pax[zf-a]: A paired box-containing gene expressed in the neural tube
-
PMID:1718739
-
Krauss S, Johansen T, Korzh V, Moens U, Ericson JU, Fjose A. Zebrafish pax[zf-a]: a paired box-containing gene expressed in the neural tube. EMBO J 1991 10:3609-19; PMID:1718739
-
(1991)
EMBO J
, vol.10
, pp. 3609-3619
-
-
Krauss, S.1
Johansen, T.2
Korzh, V.3
Moens, U.4
Ericson, J.U.5
Fjose, A.6
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