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Volumn 13, Issue 1, 2008, Pages 3-7

Epigenetics in congenital diseases and pervasive developmental disorders

Author keywords

Autism; DNA methylation; Environment; Epigenetics; Pervasive developmental disorders

Indexed keywords

AUTISM; CONGENITAL DISORDER; DEVELOPMENTAL DISORDER; DNA REPLICATION; ENVIRONMENTAL STRESS; EPIGENETICS; GENE EXPRESSION; GENE MUTATION; GENETIC DISORDER; GENOME IMPRINTING; HUMAN; NEUROLOGIC DISEASE; PHENOTYPE; REVIEW; X CHROMOSOME INACTIVATION;

EID: 42049090387     PISSN: 1342078X     EISSN: 13474715     Source Type: Journal    
DOI: 10.1007/s12199-007-0008-7     Document Type: Review
Times cited : (9)

References (33)
  • 2
    • 33645357786 scopus 로고    scopus 로고
    • 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
  • 4
    • 33646557031 scopus 로고    scopus 로고
    • Epigenetics: Unfinished symphony
    • Qiu J. Epigenetics: unfinished symphony. Nature. 2006;441:143-5.
    • (2006) Nature. , vol.441 , pp. 143-5
    • Qiu, J.1
  • 5
    • 0032076307 scopus 로고    scopus 로고
    • Imprinting in Prader-Willi and Angelman syndromes
    • Nicholls RD, Saitoh S, Horsthemke B. Imprinting in Prader-Willi and Angelman syndromes. Trends Genet. 1998;14:194-200.
    • (1998) Trends Genet. , vol.14 , pp. 194-200
    • Nicholls, R.D.1    Saitoh, S.2    Horsthemke, B.3
  • 8
    • 0033010782 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 11
    • 33847275530 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 15
    • 4444381560 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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
  • 19
    • 33846839170 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


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