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Volumn 63, Issue 6, 2004, Pages 1018-1023

Can ataxin-2 be down-regulated by allele-specific de novo DNA methylation in SCA2 patients?

Author keywords

[No Author keywords available]

Indexed keywords

ATAXIN 2; DNA; DNA METHYLTRANSFERASE; MUTANT PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

EID: 7044254730     PISSN: 03069877     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mehy.2004.03.046     Document Type: Article
Times cited : (10)

References (60)
  • 3
    • 0027164698 scopus 로고
    • Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
    • Orr H.T., Chung M.Y., Banfi S., et al. Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nat. Genet. 4(3):1993;221-226
    • (1993) Nat. Genet. , vol.4 , Issue.3 , pp. 221-226
    • Orr, H.T.1    Chung, M.Y.2    Banfi, S.3
  • 4
    • 0027162192 scopus 로고
    • Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1
    • Gispert S., Twells R., Orozco G., et al. Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1. Nat. Genet. 4(3):1993;295-299
    • (1993) Nat. Genet. , vol.4 , Issue.3 , pp. 295-299
    • Gispert, S.1    Twells, R.2    Orozco, G.3
  • 5
    • 0028143527 scopus 로고
    • CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1
    • Kawaguchi Y., Okamoto T., Taniwaki M., et al. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat. Genet. 8(3):1994;221-228
    • (1994) Nat. Genet. , vol.8 , Issue.3 , pp. 221-228
    • Kawaguchi, Y.1    Okamoto, T.2    Taniwaki, M.3
  • 6
    • 0028535670 scopus 로고
    • The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q
    • Stevanin G., Sousa P.S., Cancel G., et al. The gene for Machado-Joseph disease maps to the same 3-cM interval as the spinal cerebellar ataxia 3 gene on chromosome 14q. Neurobiol. Dis. 1(1-2):1994;79-82
    • (1994) Neurobiol. Dis. , vol.1 , Issue.12 , pp. 79-82
    • Stevanin, G.1    Sousa, P.S.2    Cancel, G.3
  • 7
    • 0031012399 scopus 로고    scopus 로고
    • Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
    • Zhuchenko O., Bailey J., Bonnen P., et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat. Genet. 15(1):1997;62-69
    • (1997) Nat. Genet. , vol.15 , Issue.1 , pp. 62-69
    • Zhuchenko, O.1    Bailey, J.2    Bonnen, P.3
  • 8
    • 0029048660 scopus 로고
    • Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p
    • Gouw L.G., Kaplan C.D., Haines J.H., et al. Retinal degeneration characterizes a spinocerebellar ataxia mapping to chromosome 3p. Nat. Genet. 10(1):1995;89-93
    • (1995) Nat. Genet. , vol.10 , Issue.1 , pp. 89-93
    • Gouw, L.G.1    Kaplan, C.D.2    Haines, J.H.3
  • 9
    • 0035393427 scopus 로고    scopus 로고
    • SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein
    • Nakamura K., Jeong S.Y., Uchihara T., et al. SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein. Hum. Mol. Genet. 10(14):2001;1441-1448
    • (2001) Hum. Mol. Genet. , vol.10 , Issue.14 , pp. 1441-1448
    • Nakamura, K.1    Jeong, S.Y.2    Uchihara, T.3
  • 10
    • 0024422743 scopus 로고
    • Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings
    • Orozco G., Estrada R., Perry T.L., et al. Dominantly inherited olivopontocerebellar atrophy from eastern Cuba. Clinical, neuropathological, and biochemical findings. J. Neurol. Sci. 93(1):1989;37-50
    • (1989) J. Neurol. Sci. , vol.93 , Issue.1 , pp. 37-50
    • Orozco, G.1    Estrada, R.2    Perry, T.L.3
  • 11
    • 0030944114 scopus 로고    scopus 로고
    • The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia
    • Geschwind D.H., Perlman S., Figueroa C.P., Treiman L.J., Pulst S.M. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. Am. J. Hum. Genet. 60(4):1997;842-850
    • (1997) Am. J. Hum. Genet. , vol.60 , Issue.4 , pp. 842-850
    • Geschwind, D.H.1    Perlman, S.2    Figueroa, C.P.3    Treiman, L.J.4    Pulst, S.M.5
  • 12
    • 0347985269 scopus 로고    scopus 로고
    • The parkinsonian phenotype of spinocerebellar ataxia type 2
    • Lu C.S., WuChou Y.H., Kuo P.C., Chang H.C., Weng Y.H. The parkinsonian phenotype of spinocerebellar ataxia type 2. Arch. Neurol. 61(1):2004;35-38
    • (2004) Arch. Neurol. , vol.61 , Issue.1 , pp. 35-38
    • Lu, C.S.1    Wuchou, Y.H.2    Kuo, P.C.3    Chang, H.C.4    Weng, Y.H.5
  • 13
    • 0037732858 scopus 로고    scopus 로고
    • SCA2 may present as levodopa-responsive parkinsonism
    • Payami H., Nutt J., Gancher S., Bird T., et al. SCA2 may present as levodopa-responsive parkinsonism. Mov. Disord. 18(4):2003;425-429
    • (2003) Mov. Disord. , vol.18 , Issue.4 , pp. 425-429
    • Payami, H.1    Nutt, J.2    Gancher, S.3    Bird, T.4
  • 14
    • 0035199626 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism
    • Shan D.E., Soong B.W., Sun C.M., Lee S.J., Liao K.K., Liu R.S. Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism. Ann. Neurol. 50(6):2001;812-815
    • (2001) Ann. Neurol. , vol.50 , Issue.6 , pp. 812-815
    • Shan, D.E.1    Soong, B.W.2    Sun, C.M.3    Lee, S.J.4    Liao, K.K.5    Liu, R.S.6
  • 15
    • 0029611008 scopus 로고
    • Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families
    • Durr A., Smadja D., Cancel G., et al. Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies). Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families. Brain. 118(6):1995;1573-1581
    • (1995) Brain , vol.118 , Issue.6 , pp. 1573-1581
    • Durr, A.1    Smadja, D.2    Cancel, G.3
  • 16
    • 8244220324 scopus 로고    scopus 로고
    • Molecular and clinical correlations in spinocerebellar ataxia 2: A study of 32 families
    • Cancel G., Durr A., Didierjean O., et al. Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families. Hum. Mol. Genet. 6(5):1997;709-715
    • (1997) Hum. Mol. Genet. , vol.6 , Issue.5 , pp. 709-715
    • Cancel, G.1    Durr, A.2    Didierjean, O.3
  • 17
    • 0030292488 scopus 로고    scopus 로고
    • Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
    • Pulst S.M., Nechiporuk A., Nechiporuk T., et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat. Genet. 14(3):1996;269-276
    • (1996) Nat. Genet. , vol.14 , Issue.3 , pp. 269-276
    • Pulst, S.M.1    Nechiporuk, A.2    Nechiporuk, T.3
  • 18
    • 0032511743 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion
    • Babovic-Vuksanovic D., Snow K., Patterson M.C., Michels V.V. Spinocerebellar ataxia type 2 (SCA 2) in an infant with extreme CAG repeat expansion. Am. J. Med. Genet. 79(5):1998;383-387
    • (1998) Am. J. Med. Genet. , vol.79 , Issue.5 , pp. 383-387
    • Babovic-Vuksanovic, D.1    Snow, K.2    Patterson, M.C.3    Michels, V.V.4
  • 19
    • 18444411305 scopus 로고    scopus 로고
    • Childhood-onset ataxia: Testing for large CAG-repeats in SCA2 and SCA7
    • Mao R., Aylsworth A.S., Potter N., et al. Childhood-onset ataxia: testing for large CAG-repeats in SCA2 and SCA7. Am. J. Med. Genet. 110(4):2002;338-345
    • (2002) Am. J. Med. Genet. , vol.110 , Issue.4 , pp. 338-345
    • Mao, R.1    Aylsworth, A.S.2    Potter, N.3
  • 20
    • 0030795968 scopus 로고    scopus 로고
    • The CAG/polyglutamine tract diseases: Gene products and molecular pathogenesis
    • Koshy B.T., Zoghbi H.Y. The CAG/polyglutamine tract diseases: gene products and molecular pathogenesis. Brain Pathol. 7(3):1997;927-942
    • (1997) Brain Pathol. , vol.7 , Issue.3 , pp. 927-942
    • Koshy, B.T.1    Zoghbi, H.Y.2
  • 21
    • 0030294345 scopus 로고    scopus 로고
    • Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
    • Imbert G., Saudou F., Yvert G., et al. Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Nat. Genet. 14(3):1996;285-291
    • (1996) Nat. Genet. , vol.14 , Issue.3 , pp. 285-291
    • Imbert, G.1    Saudou, F.2    Yvert, G.3
  • 22
    • 0031128793 scopus 로고    scopus 로고
    • SCA2 trinucleotide expansion in German SCA patients
    • Riess O., Laccone F.A., Gispert S., et al. SCA2 trinucleotide expansion in German SCA patients. Neurogenetics. 1(1):1997;59-64
    • (1997) Neurogenetics , vol.1 , Issue.1 , pp. 59-64
    • Riess, O.1    Laccone, F.A.2    Gispert, S.3
  • 23
    • 0030292368 scopus 로고    scopus 로고
    • Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
    • Sanpei K., Takano H., Igarashi S., et al. Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT. Nat. Genet. 14(3):1996;277-284
    • (1996) Nat. Genet. , vol.14 , Issue.3 , pp. 277-284
    • Sanpei, K.1    Takano, H.2    Igarashi, S.3
  • 24
    • 0038042172 scopus 로고    scopus 로고
    • Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India
    • Chattopadhyay B., Ghosh S., Gangopadhyay P.K., et al. Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India. Neurosci. Lett. 345(2):2003;93-96
    • (2003) Neurosci. Lett. , vol.345 , Issue.2 , pp. 93-96
    • Chattopadhyay, B.1    Ghosh, S.2    Gangopadhyay, P.K.3
  • 25
    • 0033867386 scopus 로고    scopus 로고
    • CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)
    • Hayes S., Turecki G., Brisebois K., et al. CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2). Hum. Mol. Genet. 9(12):2000;1753-1758
    • (2000) Hum. Mol. Genet. , vol.9 , Issue.12 , pp. 1753-1758
    • Hayes, S.1    Turecki, G.2    Brisebois, K.3
  • 26
    • 0037767510 scopus 로고    scopus 로고
    • Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell death
    • Huynh D.P., Yang H.T., Vakharia H., Nguyen D., Pulst S.M. Expansion of the polyQ repeat in ataxin-2 alters its Golgi localization, disrupts the Golgi complex and causes cell death. Hum. Mol. Genet. 12(13):2003;1485-1496
    • (2003) Hum. Mol. Genet. , vol.12 , Issue.13 , pp. 1485-1496
    • Huynh, D.P.1    Yang, H.T.2    Vakharia, H.3    Nguyen, D.4    Pulst, S.M.5
  • 27
    • 0033044001 scopus 로고    scopus 로고
    • Expression of ataxin2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2
    • Huynh D.P., Del Bigio M.R., Ho D.H., Pulst S.M. Expression of ataxin2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2. Ann. Neurol. 45(2):1999;232-241
    • (1999) Ann. Neurol. , vol.45 , Issue.2 , pp. 232-241
    • Huynh, D.P.1    Del Bigio, M.R.2    Ho, D.H.3    Pulst, S.M.4
  • 28
    • 0032840052 scopus 로고    scopus 로고
    • Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: Triple-labeling immunofluorescent study
    • Koyano S., Uchihara T., Fujigasaki H., Nakamura A., Yagishita S., Iwabuchi K. Neuronal intranuclear inclusions in spinocerebellar ataxia type 2: triple-labeling immunofluorescent study. Neurosci. Lett. 273(2):1999;117-120
    • (1999) Neurosci. Lett. , vol.273 , Issue.2 , pp. 117-120
    • Koyano, S.1    Uchihara, T.2    Fujigasaki, H.3    Nakamura, A.4    Yagishita, S.5    Iwabuchi, K.6
  • 29
    • 0036185711 scopus 로고    scopus 로고
    • Neuronal intranuclear inclusions in SCA2: A genetic, morphological and immunohistochemical study of two cases
    • Pang J.T., Giunti P., Chamberlain S., et al. Neuronal intranuclear inclusions in SCA2: a genetic, morphological and immunohistochemical study of two cases. Brain. 125(Pt 3):2002;656-663
    • (2002) Brain , vol.125 , Issue.3 PART , pp. 656-663
    • Pang, J.T.1    Giunti, P.2    Chamberlain, S.3
  • 30
    • 0032970447 scopus 로고    scopus 로고
    • Clinical and molecular analysis of 11 Sicilian SCA2 families: Influence of gender on age at onset
    • Giuffrida S., Lanza S., Restivo D.A., et al. Clinical and molecular analysis of 11 Sicilian SCA2 families: influence of gender on age at onset. Eur. J. Neurol. 6(3):1999;301-307
    • (1999) Eur. J. Neurol. , vol.6 , Issue.3 , pp. 301-307
    • Giuffrida, S.1    Lanza, S.2    Restivo, D.A.3
  • 31
    • 6844236985 scopus 로고    scopus 로고
    • The natural history of degenerative ataxia: A retrospective study in 466 patients
    • Klockgether T., Ludtke R., Kramer B., et al. The natural history of degenerative ataxia: a retrospective study in 466 patients. Brain. 121(Pt 4):1998;589-600
    • (1998) Brain , vol.121 , Issue.4 PART , pp. 589-600
    • Klockgether, T.1    Ludtke, R.2    Kramer, B.3
  • 33
    • 0033582337 scopus 로고    scopus 로고
    • Identification of the physiological promoter for spinocerebellar ataxia 2 gene reveals a CpG island for promoter activity situated into the exon 1 of this gene and provides data about the origin of the nonmethylated state of these types of islands
    • Aguiar J., Santurlidis S., Nowok J., et al. Identification of the physiological promoter for spinocerebellar ataxia 2 gene reveals a CpG island for promoter activity situated into the exon 1 of this gene and provides data about the origin of the nonmethylated state of these types of islands. Biochem. Biophys. Res. Commun. 254(2):1999;315-318
    • (1999) Biochem. Biophys. Res. Commun. , vol.254 , Issue.2 , pp. 315-318
    • Aguiar, J.1    Santurlidis, S.2    Nowok, J.3
  • 34
    • 0035839057 scopus 로고    scopus 로고
    • The role of DNA methylation in mammalian epigenetics
    • Jones P.A., Takai D. The role of DNA methylation in mammalian epigenetics. Science. 293(5532):2001;1068-1070
    • (2001) Science , vol.293 , Issue.5532 , pp. 1068-1070
    • Jones, P.A.1    Takai, D.2
  • 35
    • 0036144048 scopus 로고    scopus 로고
    • DNA methylation patterns and epigenetic memory
    • Bird A. DNA methylation patterns and epigenetic memory. Genes Dev. 16(1):2002;6-21
    • (2002) Genes Dev. , vol.16 , Issue.1 , pp. 6-21
    • Bird, A.1
  • 36
    • 0036613432 scopus 로고    scopus 로고
    • Role for DNA methylation in the control of cell type specific maspin expression
    • Futscher B.W., Oshiro M.M., Wozniak R.J., et al. Role for DNA methylation in the control of cell type specific maspin expression. Nat. Genet. 31(2):2002;175-179
    • (2002) Nat. Genet. , vol.31 , Issue.2 , pp. 175-179
    • Futscher, B.W.1    Oshiro, M.M.2    Wozniak, R.J.3
  • 37
    • 0036230566 scopus 로고    scopus 로고
    • A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes
    • Strichman-Almashanu L.Z., Lee R.S., Onyango P.O., et al. A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes. Genome Res. 12(4):2002;543-554
    • (2002) Genome Res. , vol.12 , Issue.4 , pp. 543-554
    • Strichman-Almashanu, L.Z.1    Lee, R.S.2    Onyango, P.O.3
  • 39
    • 0029126403 scopus 로고
    • DNA methylation in early development
    • Razin A., Shemer R. DNA methylation in early development. Hum. Mol. Genet. 4(Spec No):1995;1751-1755
    • (1995) Hum. Mol. Genet. , vol.4 , Issue.SPEC. NO. , pp. 1751-1755
    • Razin, A.1    Shemer, R.2
  • 40
    • 0023503627 scopus 로고
    • Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse
    • Sanford J.P., Clark H.J., Chapman V.M., Rossant J. Differences in DNA methylation during oogenesis and spermatogenesis and their persistence during early embryogenesis in the mouse. Genes Dev. 1(10):1987;1039-1046
    • (1987) Genes Dev. , vol.1 , Issue.10 , pp. 1039-1046
    • Sanford, J.P.1    Clark, H.J.2    Chapman, V.M.3    Rossant, J.4
  • 41
    • 0030921218 scopus 로고    scopus 로고
    • Activation of the lac repressor in the transgenic mouse
    • Scrable H., Stambrook P.J. Activation of the lac repressor in the transgenic mouse. Genetics. 147(1):1997;297-304
    • (1997) Genetics , vol.147 , Issue.1 , pp. 297-304
    • Scrable, H.1    Stambrook, P.J.2
  • 42
    • 0032756518 scopus 로고    scopus 로고
    • The establishment and maintenance of DNA methylation patterns in mouse somatic cells
    • Turker M.S. The establishment and maintenance of DNA methylation patterns in mouse somatic cells. Semin Cancer Biol. 9(5):1999;329-337
    • (1999) Semin Cancer Biol. , vol.9 , Issue.5 , pp. 329-337
    • Turker, M.S.1
  • 43
    • 0032570260 scopus 로고    scopus 로고
    • Influence of pre-existing methylation on the de novo activity of eukaryotic DNA methyltransferase
    • Carotti D., Funiciello S., Palitti F., Strom R. Influence of pre-existing methylation on the de novo activity of eukaryotic DNA methyltransferase. Biochemistry. 37(4):1998;1101-1108
    • (1998) Biochemistry , vol.37 , Issue.4 , pp. 1101-1108
    • Carotti, D.1    Funiciello, S.2    Palitti, F.3    Strom, R.4
  • 44
    • 0031580212 scopus 로고    scopus 로고
    • Control of methylation spreading in synthetic DNA sequences by the murine DNA methyltransferase
    • Tollefsbol T.O., Hutchison III C.S. Control of methylation spreading in synthetic DNA sequences by the murine DNA methyltransferase. J. Mol. Biol. 269(4):1997;494-504
    • (1997) J. Mol. Biol. , vol.269 , Issue.4 , pp. 494-504
    • Tollefsbol, T.O.1    Hutchison III, C.S.2
  • 45
    • 0029853519 scopus 로고    scopus 로고
    • Spreading of methylation along DNA
    • Lindsay H., Adams L.P. Spreading of methylation along DNA. Biochem. J. 320(pt 2):1996;473-478
    • (1996) Biochem. J. , vol.320 , Issue.2 PART , pp. 473-478
    • Lindsay, H.1    Adams, L.P.2
  • 46
    • 0024672415 scopus 로고
    • Genomic sequencing reveals a 5-methylcytosine-free domain in active promoters and the spreading of preimposed methylation patterns
    • Toth M., Lichtenberg U., Doerfler W. Genomic sequencing reveals a 5-methylcytosine-free domain in active promoters and the spreading of preimposed methylation patterns. Proc. Natl. Acad. Sci. USA. 86(10):1989;3728-3732
    • (1989) Proc. Natl. Acad. Sci. USA , vol.86 , Issue.10 , pp. 3728-3732
    • Toth, M.1    Lichtenberg, U.2    Doerfler, W.3
  • 47
    • 0031835780 scopus 로고    scopus 로고
    • Cis-Acting signal for inheritance of imprinted DNA methylation patterns in the preimplantation mouse embryo
    • Howell C.Y., Steptoes A.L., Miller M.W., Chaillet J.R. cis-Acting signal for inheritance of imprinted DNA methylation patterns in the preimplantation mouse embryo. Mol. Cell. Biol. 18(7):1998;4149-4156
    • (1998) Mol. Cell. Biol. , vol.18 , Issue.7 , pp. 4149-4156
    • Howell, C.Y.1    Steptoes, A.L.2    Miller, M.W.3    Chaillet, J.R.4
  • 48
    • 0025851721 scopus 로고
    • Region and cell type-specific de novo DNA methylation in cultured mammalian cells
    • Turker M.S., Mummaneni P., Bishop P.L. Region and cell type-specific de novo DNA methylation in cultured mammalian cells. Somat. Cell. Mol. Genet. 17(2):1991;151-157
    • (1991) Somat. Cell. Mol. Genet. , vol.17 , Issue.2 , pp. 151-157
    • Turker, M.S.1    Mummaneni, P.2    Bishop, P.L.3
  • 49
    • 0025364877 scopus 로고
    • A DNA signal from Thy-1 defines de novo methylation patterns in embryonic stem cells
    • Szyf A., Tanigawa G., McCarthy P.L. Jr. A DNA signal from Thy-1 defines de novo methylation patterns in embryonic stem cells. Mol. Cell. Biol. 10(8):1990;4396-4400
    • (1990) Mol. Cell. Biol. , vol.10 , Issue.8 , pp. 4396-4400
    • Szyf, A.1    Tanigawa, G.2    McCarthy Jr., P.L.3
  • 50
    • 0026439115 scopus 로고
    • A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei
    • Leonhardt H., Page A.W., Weirer H.U., Bestor T.H. A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei. Cell. 71(5):1992;865-873
    • (1992) Cell , vol.71 , Issue.5 , pp. 865-873
    • Leonhardt, H.1    Page, A.W.2    Weirer, H.U.3    Bestor, T.H.4
  • 51
    • 0026008102 scopus 로고
    • Recognition of unusual DNA structures by human DNA (cytosine-5) methyltransferase
    • Smith S.S., Kan J.L.C., Baker D.J., Kaplan B.E., Dembek P. Recognition of unusual DNA structures by human DNA (cytosine-5) methyltransferase. J. Mol. Biol. 217(1):1991;39-51
    • (1991) J. Mol. Biol. , vol.217 , Issue.1 , pp. 39-51
    • Smith, S.S.1    Kan, J.L.C.2    Baker, D.J.3    Kaplan, B.E.4    Dembek, P.5
  • 52
    • 0029008288 scopus 로고
    • Hairpins are formed by the single DNA strands of the fragile X triplet repeats: Structure and biological implications
    • Chen X., Mariappan S.V., Catasti P., et al. Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications. Proc. Natl. Acad. Sci. USA. 92(11):1995;5199-5203
    • (1995) Proc. Natl. Acad. Sci. USA , vol.92 , Issue.11 , pp. 5199-5203
    • Chen, X.1    Mariappan, S.V.2    Catasti, P.3
  • 53
    • 0033615717 scopus 로고    scopus 로고
    • DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development
    • Okano M., Bell D.W., Haber D.A., Li E. DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell. 99(3):1999;247-257
    • (1999) Cell , vol.99 , Issue.3 , pp. 247-257
    • Okano, M.1    Bell, D.W.2    Haber, D.A.3    Li, E.4
  • 54
    • 0029053371 scopus 로고
    • Trinucleotide repeats that expand in human disease form hairpin structures in vitro
    • Gacy A.M., Goellner G., Juranic N., Macura S., McMurray C.T. Trinucleotide repeats that expand in human disease form hairpin structures in vitro. Cell. 81(4):1995;533-540
    • (1995) Cell , vol.81 , Issue.4 , pp. 533-540
    • Gacy, A.M.1    Goellner, G.2    Juranic, N.3    MacUra, S.4    McMurray, C.T.5
  • 55
    • 0028864764 scopus 로고
    • DNA CTG triplet repeats involved in dynamic mutations of neurologically related gene sequences form stable duplexes
    • Smith G.K., Jie J., Fox G.E., Gao X. DNA CTG triplet repeats involved in dynamic mutations of neurologically related gene sequences form stable duplexes. Nucleic Acids Res. 23(21):1995;4303-4311
    • (1995) Nucleic Acids Res. , vol.23 , Issue.21 , pp. 4303-4311
    • Smith, G.K.1    Jie, J.2    Fox, G.E.3    Gao, X.4
  • 56
    • 0028889383 scopus 로고
    • The purine-rich trinucleotide repeat sequences d(CAG)15 and d(GAC)15 form hairpins
    • Yu A., Dill J., Mitas M. The purine-rich trinucleotide repeat sequences d(CAG)15 and d(GAC)15 form hairpins. Nucleic Acids Res. 23(20):1995;4055-4057
    • (1995) Nucleic Acids Res. , vol.23 , Issue.20 , pp. 4055-4057
    • Yu, A.1    Dill, J.2    Mitas, M.3
  • 57
    • 0030737538 scopus 로고    scopus 로고
    • Trinucleotide repeats associated with human disease
    • Mitas M. Trinucleotide repeats associated with human disease. Nucleic Acids Res. 25(12):1997;2245-2254
    • (1997) Nucleic Acids Res. , vol.25 , Issue.12 , pp. 2245-2254
    • Mitas, M.1
  • 58
    • 0035504107 scopus 로고    scopus 로고
    • CAG repeat instability at SCA2 locus: Anchoring CAA interruptions and linked single nucleotide polymorphisms
    • Choudhry S., Mukerji M., Srivastava A.K., Jain S., Brahmachari S.K. CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms. Hum. Mol. Genet. 10(21):2001;2437-2446
    • (2001) Hum. Mol. Genet. , vol.10 , Issue.21 , pp. 2437-2446
    • Choudhry, S.1    Mukerji, M.2    Srivastava, A.K.3    Jain, S.4    Brahmachari, S.K.5
  • 59
    • 0028920604 scopus 로고
    • The mechanism of inhibition of DNA (cytosine-5-)-methyltransferases by 5-azacytosine is likely to involve methyl transfer to the inhibitor
    • Gabbara S., Bhagwat A.S. The mechanism of inhibition of DNA (cytosine-5-)-methyltransferases by 5-azacytosine is likely to involve methyl transfer to the inhibitor. Biochem. J. 307(Pt1):1995;87-92
    • (1995) Biochem. J. , vol.307 , Issue.1 PART , pp. 87-92
    • Gabbara, S.1    Bhagwat, A.S.2
  • 60
    • 0000418476 scopus 로고
    • Covalent bond formation between a DNA-cytosine methyltransferase and DNA containing 5-azacytosine
    • Santi D.V., Norment A., Garrett C.E. Covalent bond formation between a DNA-cytosine methyltransferase and DNA containing 5-azacytosine. Proc. Natl. Acad. Sci. USA. 81(22):1984;6993-6997
    • (1984) Proc. Natl. Acad. Sci. USA , vol.81 , Issue.22 , pp. 6993-6997
    • Santi, D.V.1    Norment, A.2    Garrett, C.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.