-
1
-
-
3342989681
-
Epigenetic programming by maternal behavior
-
Weaver IC, Cervoni N, Champagne FA, D'Alessio AC, Sharma S, Seckl JR, et al. Epigenetic programming by maternal behavior. Nat Neurosci. 2004;7:847-54.
-
(2004)
Nat Neurosci.
, vol.7
, pp. 847-54
-
-
Weaver, I.C.1
Cervoni, N.2
Champagne, F.A.3
D'Alessio, A.C.4
Sharma, S.5
Seckl, J.R.6
-
2
-
-
33645357786
-
Sustained hippocampal chromatin regulation in a mouse model of depression and antidepressant action
-
Tsankova NM, Berton O, Renthal W, Kumar A, Neve RL, Nestler EJ. Sustained hippocampal chromatin regulation in a mouse model of depression and antidepressant action. Nat Neurosci. 2006;9:519-25.
-
(2006)
Nat Neurosci.
, vol.9
, pp. 519-25
-
-
Tsankova, N.M.1
Berton, O.2
Renthal, W.3
Kumar, A.4
Neve, R.L.5
Nestler, E.J.6
-
3
-
-
23044514669
-
Epigenetic differences arise during the lifetime of monozygotic twins
-
Fraga MF, Ballestar E, Paz MF, Ropero S, Setien F, Ballestar ML, et al. Epigenetic differences arise during the lifetime of monozygotic twins. Proc Natl Acad Sci USA. 2005;102:10604-9.
-
(2005)
Proc Natl Acad Sci USA.
, vol.102
, pp. 10604-9
-
-
Fraga, M.F.1
Ballestar, E.2
Paz, M.F.3
Ropero, S.4
Setien, F.5
Ballestar, M.L.6
-
4
-
-
33646557031
-
Epigenetics: Unfinished symphony
-
Qiu J. Epigenetics: unfinished symphony. Nature. 2006;441:143-5.
-
(2006)
Nature.
, vol.441
, pp. 143-5
-
-
Qiu, J.1
-
6
-
-
0031133081
-
Methylation-specific PCR symplifies imprinting analysis
-
Kubota T, Das S, Christian SL, Baylin SB, Herman JG, Ledbetter DH. Methylation-specific PCR symplifies imprinting analysis. Nat Genet. 1997;16:16-7.
-
(1997)
Nat Genet.
, vol.16
, pp. 16-7
-
-
Kubota, T.1
Das, S.2
Christian, S.L.3
Baylin, S.B.4
Herman, J.G.5
Ledbetter, D.H.6
-
7
-
-
16944364326
-
Autism or atypical autism in maternally but not paternally derived proximal 15q duplication
-
Cook EH Jr, Lindgren V, Leventhal BL, Courchesne R, Lincoln A, Shulman C, et al. Autism or atypical autism in maternally but not paternally derived proximal 15q duplication. Am J Hum Genet. 1997;60:928-34.
-
(1997)
Am J Hum Genet.
, vol.60
, pp. 928-34
-
-
Cook Jr., E.H.1
Lindgren, V.2
Leventhal, B.L.3
Courchesne, R.4
Lincoln, A.5
Shulman, C.6
-
8
-
-
0033010782
-
A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR
-
Kubota T, Nonoyama S, Tonoki H, Masuno M, Imaizumi K, Kojima M, et al. A new assay for the analysis of X-chromosome inactivation based on methylation-specific PCR. Hum Genet. 1999;104:49-55.
-
(1999)
Hum Genet.
, vol.104
, pp. 49-55
-
-
Kubota, T.1
Nonoyama, S.2
Tonoki, H.3
Masuno, M.4
Imaizumi, K.5
Kojima, M.6
-
9
-
-
0036613514
-
Aberrant patterns of X chromosome inactivation in bovine clones
-
Xue F, Tian XC, Du F, Kubota C, Taneja M, Dinnyes A, et al. Aberrant patterns of X chromosome inactivation in bovine clones. Nat Genet. 2002;31:216-20.
-
(2002)
Nat Genet.
, vol.31
, pp. 216-20
-
-
Xue, F.1
Tian, X.C.2
Du, F.3
Kubota, C.4
Taneja, M.5
Dinnyes, A.6
-
10
-
-
14544271451
-
X chromosome reactivation and regulation in cloned embryos
-
Nolen LD, Gao S, Han Z, Mann MR, Gie Chung Y, Otte AP, et al. X chromosome reactivation and regulation in cloned embryos. Dev Biol. 2005;279:525-40.
-
(2005)
Dev Biol.
, vol.279
, pp. 525-40
-
-
Nolen, L.D.1
Gao, S.2
Han, Z.3
Mann, M.R.4
Gie Chung, Y.5
Otte, A.P.6
-
11
-
-
33847275530
-
Nuclear reprogramming of cloned embryos and its implications for therapeutic cloning
-
Yang X, Smith SL, Tian XC, Lewin HA, Renard JP, Wakayama T. Nuclear reprogramming of cloned embryos and its implications for therapeutic cloning. Nat Genet. 2007;39:295-302.
-
(2007)
Nat Genet.
, vol.39
, pp. 295-302
-
-
Yang, X.1
Smith, S.L.2
Tian, X.C.3
Lewin, H.A.4
Renard, J.P.5
Wakayama, T.6
-
12
-
-
10744230718
-
Proportion of the cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females
-
Kubota T, Wakui K, Nakamura T, Ohashi H, Watanabe Y, Yoshino M, et al. Proportion of the cells with functional X disomy is associated with the severity of mental retardation in mosaic ring X Turner syndrome females. Cytogenet Genome Res. 2002;99:276-84.
-
(2002)
Cytogenet Genome Res.
, vol.99
, pp. 276-84
-
-
Kubota, T.1
Wakui, K.2
Nakamura, T.3
Ohashi, H.4
Watanabe, Y.5
Yoshino, M.6
-
13
-
-
0033615717
-
DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
-
Okano M, Bell DW, Haber DA, Li E. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell 1999;99:247-57.
-
(1999)
Cell.
, vol.99
, pp. 247-57
-
-
Okano, M.1
Bell, D.W.2
Haber, D.A.3
Li, E.4
-
14
-
-
0037105006
-
Three novel DNMT3B mutations in Japanese patients with ICF syndrome
-
Shirohzu H, Kubota T, Kumazawa A, Sado T, Chijiwa T, Inagaki K, et al. Three novel DNMT3B mutations in Japanese patients with ICF syndrome. Am J Med Genet. 2002;112:31-7.
-
(2002)
Am J Med Genet.
, vol.112
, pp. 31-7
-
-
Shirohzu, H.1
Kubota, T.2
Kumazawa, A.3
Sado, T.4
Chijiwa, T.5
Inagaki, K.6
-
15
-
-
4444381560
-
ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutation
-
Kubota T, Furuumi H, Kamoda T, Iwasaki N, Tobita N, Fujiwara N, et al. ICF syndrome in a girl with DNA hypomethylation but without detectable DNMT3B mutation. Am J Med Genet A. 2004;129:290-3.
-
(2004)
Am J Med Genet A.
, vol.129
, pp. 290-3
-
-
Kubota, T.1
Furuumi, H.2
Kamoda, T.3
Iwasaki, N.4
Tobita, N.5
Fujiwara, N.6
-
16
-
-
0032830639
-
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
-
Amir RE, Van den Veyver IB, Wan M, Tran CQ, Francke U, Zoghbi HY. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Nat Genet. 1999;23:185-8.
-
(1999)
Nat Genet.
, vol.23
, pp. 185-8
-
-
Amir, R.E.1
Van Den Veyver, I.B.2
Wan, M.3
Tran, C.Q.4
Francke, U.5
Zoghbi, H.Y.6
-
17
-
-
33751006767
-
A patient with classic Rett syndrome with a novel mutation in MECP2 exon 1
-
Chunshu Y, Endoh K, Soutome M, Kawamura R, Kubota T. A patient with classic Rett syndrome with a novel mutation in MECP2 exon 1. Clin Genet. 2006;70:530-1.
-
(2006)
Clin Genet.
, vol.70
, pp. 530-1
-
-
Chunshu, Y.1
Endoh, K.2
Soutome, M.3
Kawamura, R.4
Kubota, T.5
-
18
-
-
0242332183
-
-
Chen WG, Chang Q, Lin Y, Meissner A, West AE, Griffith EC, et al. Derepression of BDNF transcription involves. calcium-dependent phosphorylation of MeCP2. Science. 2003;302:885-9.
-
(2003)
Science.
, vol.302
, pp. 885-9
-
-
Chen, W.G.1
Chang, Q.2
Lin, Y.3
Meissner, A.4
West, A.E.5
Griffith, E.C.6
-
19
-
-
33846839170
-
Methyl CpG-binding protein 2, whose mutation causes Rett syndrome, directly regulates insulin-like growth factor binding protein 3 in mouse and human Brains
-
Itoh M, Ide S, Takashima S, Kudo S, Nomura Y, Segawa M, et al. Methyl CpG-binding protein 2, whose mutation causes Rett syndrome, directly regulates insulin-like growth factor binding protein 3 in mouse and human Brains. J Neuropathol Exp Neurol. 2007;66:117-23.
-
(2007)
J Neuropathol Exp Neurol.
, vol.66
, pp. 117-23
-
-
Itoh, M.1
Ide, S.2
Takashima, S.3
Kudo, S.4
Nomura, Y.5
Segawa, M.6
-
20
-
-
0031873353
-
Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice
-
Wolff GL, Kodell RL, Moore SR, Cooney CA. Maternal epigenetics and methyl supplements affect agouti gene expression in Avy/a mice. FASEB J. 1998;12:949-57.
-
(1998)
FASEB J.
, vol.12
, pp. 949-57
-
-
Wolff, G.L.1
Kodell, R.L.2
Moore, S.R.3
Cooney, C.A.4
-
21
-
-
33144488275
-
Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus
-
Waterland RA, Lin JR, Smith CA, Jirtle RL. Post-weaning diet affects genomic imprinting at the insulin-like growth factor 2 (Igf2) locus. Hum Mol Genet. 2006;15:705-16.
-
(2006)
Hum Mol Genet.
, vol.15
, pp. 705-16
-
-
Waterland, R.A.1
Lin, J.R.2
Smith, C.A.3
Jirtle, R.L.4
-
22
-
-
15244348759
-
Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism
-
James SJ, Cutler P, Melnyk S, Jernigan S, Janak L, Gaylor DW, et al. Metabolic biomarkers of increased oxidative stress and impaired methylation capacity in children with autism. Am J Clin Nutr. 2004;80:1611-7.
-
(2004)
Am J Clin Nutr.
, vol.80
, pp. 1611-7
-
-
James, S.J.1
Cutler, P.2
Melnyk, S.3
Jernigan, S.4
Janak, L.5
Gaylor, D.W.6
-
23
-
-
0017805106
-
The effect of high doses of vitamin B6 on autistic children: A double-blind crossover study
-
Rimland B, Callaway E, Dreyfus P. The effect of high doses of vitamin B6 on autistic children: a double-blind crossover study. Am J Psychiatry. 1978;135:472-5.
-
(1978)
Am J Psychiatry.
, vol.135
, pp. 472-5
-
-
Rimland, B.1
Callaway, E.2
Dreyfus, P.3
-
25
-
-
0023739206
-
Controversies in the treatment of autistic children: Vitamin and drug therapy
-
Suppl
-
Rimland B. Controversies in the treatment of autistic children: vitamin and drug therapy. J Child Neurol. 1988;3[Suppl]:S68-S72.
-
(1988)
J Child Neurol.
, vol.3
-
-
Rimland, B.1
-
26
-
-
20144366421
-
Cerebral folate deficiency with developmental delay, autism, and response to folinic acid
-
Moretti P, Sahoo T, Hyland K, Bottiglieri T, Peters S, del Gaudio D, et al. Cerebral folate deficiency with developmental delay, autism, and response to folinic acid. Neurology. 2005;64:1088-90.
-
(2005)
Neurology.
, vol.64
, pp. 1088-90
-
-
Moretti, P.1
Sahoo, T.2
Hyland, K.3
Bottiglieri, T.4
Peters, S.5
Del Gaudio, D.6
-
27
-
-
33750488776
-
No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy
-
van der Kooi EL, de Greef JC, Wohlgemuth M, Frants RR, van Asseldonk RJ, Blom HJ, et al. No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy. Neuromuscul Disord. 2006;16:766-9.
-
(2006)
Neuromuscul Disord.
, vol.16
, pp. 766-9
-
-
Van Der Kooi, E.L.1
De Greef, J.C.2
Wohlgemuth, M.3
Frants, R.R.4
Van Asseldonk, R.J.5
Blom, H.J.6
-
28
-
-
34249930701
-
Short hairpin RNA causes the methylation of transforming growth factor-beta receptor II promoter and silencing of the target gene in rat hepatic stellate cells
-
Kim JW, Zhang YH, Zern MA, Rossi JJ, Wu J. Short hairpin RNA causes the methylation of transforming growth factor-beta receptor II promoter and silencing of the target gene in rat hepatic stellate cells. Biochem Biophys Res Commun. 2007;359:292-7.
-
(2007)
Biochem Biophys Res Commun.
, vol.359
, pp. 292-7
-
-
Kim, J.W.1
Zhang, Y.H.2
Zern, M.A.3
Rossi, J.J.4
Wu, J.5
-
29
-
-
20344379701
-
Environmental influences during development and their later consequences for health and disease: Implications for the interpretation of empirical studies
-
Gluckman PD, Hanson MA, Spencer HG, Bateson P. Environmental influences during development and their later consequences for health and disease: implications for the interpretation of empirical studies. Proc Biol Sci. 2005;272:671-7.
-
(2005)
Proc Biol Sci.
, vol.272
, pp. 671-7
-
-
Gluckman, P.D.1
Hanson, M.A.2
Spencer, H.G.3
Bateson, P.4
-
30
-
-
34249279527
-
Stability and flexibility of epigenetic gene regulation in mammalian development
-
Reik W. Stability and flexibility of epigenetic gene regulation in mammalian development. Nature. 2007;447:425-32.
-
(2007)
Nature.
, vol.447
, pp. 425-32
-
-
Reik, W.1
-
31
-
-
0035958326
-
Pervasive developmental disorders in young children
-
Hyman SL, Rodier PM, Davidson P. Pervasive developmental disorders in young children. JAMA. 2001;285:3141-2.
-
(2001)
JAMA.
, vol.285
, pp. 3141-2
-
-
Hyman, S.L.1
Rodier, P.M.2
Davidson, P.3
-
32
-
-
33745818375
-
Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: The Special Needs and Autism Project (SNAP)
-
Baird G, Simonoff E, Pickles A, Chandler S, Loucas T, Meldrum D, et al. Prevalence of disorders of the autism spectrum in a population cohort of children in South Thames: the Special Needs and Autism Project (SNAP). Lancet. 2006;368:210-5.
-
(2006)
Lancet.
, vol.368
, pp. 210-5
-
-
Baird, G.1
Simonoff, E.2
Pickles, A.3
Chandler, S.4
Loucas, T.5
Meldrum, D.6
-
33
-
-
0036304235
-
Intracytoplasmic sperm injection may increase the risk of imprinting defects
-
Burger J, Lip V, Mau UA, Sperling K, Wu BL, Horsthemke B. Intracytoplasmic sperm injection may increase the risk of imprinting defects. Am J Hum Genet. 2002;71:162-4.
-
(2002)
Am J Hum Genet.
, vol.71
, pp. 162-4
-
-
Burger, J.1
Lip, V.2
Mau, U.A.3
Sperling, K.4
Wu, B.L.5
Horsthemke, B.6
|