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Volumn 19, Issue 11, 2010, Pages 2177-2190

Elevated expression of MeCP2 in cardiac and skeletal tissues is detrimental for normal development

Author keywords

[No Author keywords available]

Indexed keywords

METHYL CPG BINDING PROTEIN 2; ALCIAN BLUE; ALIZARIN; ANTHRAQUINONE DERIVATIVE; BROXURIDINE; MECP2 PROTEIN, MOUSE; PRIMER DNA;

EID: 77953533210     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddq096     Document Type: Article
Times cited : (42)

References (99)
  • 1
    • 0036144048 scopus 로고    scopus 로고
    • DNA methylation patterns and epigenetic memory
    • Bird, A. (2002) DNA methylation patterns and epigenetic memory. Genes Dev., 16, 6-21.
    • (2002) Genes Dev. , vol.16 , pp. 6-21
    • Bird, A.1
  • 2
    • 15744401773 scopus 로고    scopus 로고
    • Eukaryotic cytosine methyltransferases
    • Goll, M.G. and Bestor, T.H. (2005) Eukaryotic cytosine methyltransferases. Annu. Rev. Biochem., 74, 481-514.
    • (2005) Annu. Rev. Biochem. , vol.74 , pp. 481-514
    • Goll, M.G.1    Bestor, T.H.2
  • 4
    • 0026708177 scopus 로고
    • Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
    • Li, E., Bestor, T.H. and Jaenisch, R. (1992) Targeted mutation of the DNA methyltransferase gene results in embryonic lethality. Cell, 69, 915-926.
    • (1992) Cell , vol.69 , pp. 915-926
    • Li, E.1    Bestor, T.H.2    Jaenisch, R.3
  • 5
    • 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. and Li, E. (1999) DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development. Cell, 99, 247-257.
    • (1999) Cell , vol.99 , pp. 247-257
    • Okano, M.1    Bell, D.W.2    Haber, D.A.3    Li, E.4
  • 6
    • 34547925220 scopus 로고    scopus 로고
    • Construction and evolution of imprinted loci in mammals
    • Hore, T.A., Rapkins, R.W. and Graves, J.A. (2007) Construction and evolution of imprinted loci in mammals. Trends Genet., 23, 440-448.
    • (2007) Trends Genet. , vol.23 , pp. 440-448
    • Hore, T.A.1    Rapkins, R.W.2    Graves, J.A.3
  • 7
    • 34848911647 scopus 로고    scopus 로고
    • DNA methylation: the nuts and bolts of repression
    • Miranda, T.B. and Jones, P.A. (2007) DNA methylation: the nuts and bolts of repression. J. Cell Physiol., 213, 384-390.
    • (2007) J. Cell Physiol. , vol.213 , pp. 384-390
    • Miranda, T.B.1    Jones, P.A.2
  • 8
    • 34548627662 scopus 로고    scopus 로고
    • A cross-species comparison of X-chromosome inactivation in Eutheria
    • Yen, Z.C., Meyer, I.M., Karalic, S. and Brown, C.J. (2007) A cross-species comparison of X-chromosome inactivation in Eutheria. Genomics, 90, 453-463.
    • (2007) Genomics , vol.90 , pp. 453-463
    • Yen, Z.C.1    Meyer, I.M.2    Karalic, S.3    Brown, C.J.4
  • 9
    • 38049164130 scopus 로고    scopus 로고
    • Activation and transposition of endogenous retroviral elements in hypomethylation induced tumors in mice
    • Howard, G., Eiges, R., Gaudet, F., Jaenisch, R. and Eden, A. (2008) Activation and transposition of endogenous retroviral elements in hypomethylation induced tumors in mice. Oncogene, 27, 404-408.
    • (2008) Oncogene , vol.27 , pp. 404-408
    • Howard, G.1    Eiges, R.2    Gaudet, F.3    Jaenisch, R.4    Eden, A.5
  • 10
    • 0030840954 scopus 로고    scopus 로고
    • Cytosine methylation and the ecology of intragenomic parasites
    • Yoder, J.A., Walsh, C.P. and Bestor, T.H. (1997) Cytosine methylation and the ecology of intragenomic parasites. Trends Genet., 13, 335-340.
    • (1997) Trends Genet. , vol.13 , pp. 335-340
    • Yoder, J.A.1    Walsh, C.P.2    Bestor, T.H.3
  • 11
    • 34249279527 scopus 로고    scopus 로고
    • Stability and flexibility of epigenetic gene regulation in mammalian development
    • Reik, W. (2007) Stability and flexibility of epigenetic gene regulation in mammalian development. Nature, 447, 425-432.
    • (2007) Nature , vol.447 , pp. 425-432
    • Reik, W.1
  • 12
    • 33845745757 scopus 로고    scopus 로고
    • Epigenetic marks in cloned rhesus monkey embryos: comparison with counterparts produced in vitro
    • Yang, J., Yang, S., Beaujean, N., Niu, Y., He, X., Xie, Y., Tang, X., Wang, L., Zhou, Q. and Ji, W. (2007) Epigenetic marks in cloned rhesus monkey embryos: comparison with counterparts produced in vitro. Biol. Reprod., 76, 36-42.
    • (2007) Biol. Reprod. , vol.76 , pp. 36-42
    • Yang, J.1    Yang, S.2    Beaujean, N.3    Niu, Y.4    He, X.5    Xie, Y.6    Tang, X.7    Wang, L.8    Zhou, Q.9    Ji, W.10
  • 13
    • 36549056015 scopus 로고    scopus 로고
    • Epigenetic changes in cancer
    • Gronbaek, K., Hother, C. and Jones, P.A. (2007) Epigenetic changes in cancer. APMIS, 115, 1039-1059.
    • (2007) APMIS , vol.115 , pp. 1039-1059
    • Gronbaek, K.1    Hother, C.2    Jones, P.A.3
  • 15
    • 34247479414 scopus 로고    scopus 로고
    • Epigenetic decisions in mammalian germ cells
    • Schaefer, C.B., Ooi, S.K., Bestor, T.H. and Bourc'his, D. (2007) Epigenetic decisions in mammalian germ cells. Science, 316, 398-399.
    • (2007) Science , vol.316 , pp. 398-399
    • Schaefer, C.B.1    Ooi, S.K.2    Bestor, T.H.3    Bourc'his, D.4
  • 16
    • 33749594205 scopus 로고    scopus 로고
    • DNA methyltransferase 1 knockdown activates a replication stress checkpoint
    • Unterberger, A., Andrews, S.D., Weaver, I.C. and Szyf, M. (2006) DNA methyltransferase 1 knockdown activates a replication stress checkpoint. Mol. Cell Biol., 26, 7575-7586.
    • (2006) Mol. Cell Biol. , vol.26 , pp. 7575-7586
    • Unterberger, A.1    Andrews, S.D.2    Weaver, I.C.3    Szyf, M.4
  • 17
    • 0031792779 scopus 로고    scopus 로고
    • Identification and characterization of a family of mammalian methyl-CpG binding proteins
    • Hendrich, B. and Bird, A. (1998) Identification and characterization of a family of mammalian methyl-CpG binding proteins. Mol. Cell Biol., 18, 6538-6547.
    • (1998) Mol. Cell Biol. , vol.18 , pp. 6538-6547
    • Hendrich, B.1    Bird, A.2
  • 18
    • 0027495467 scopus 로고
    • Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2
    • Nan, X., Meehan, R.R. and Bird, A. (1993) Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2. Nucleic Acids Res., 21, 4886-4892.
    • (1993) Nucleic Acids Res. , vol.21 , pp. 4886-4892
    • Nan, X.1    Meehan, R.R.2    Bird, A.3
  • 20
    • 0032574977 scopus 로고    scopus 로고
    • Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
    • Nan, X., Ng, H.H., Johnson, C.A., Laherty, C.D., Turner, B.M., Eisenman, R.N. and Bird, A. (1998) Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex. Nature, 393, 386-389.
    • (1998) Nature , vol.393 , pp. 386-389
    • Nan, X.1    Ng, H.H.2    Johnson, C.A.3    Laherty, C.D.4    Turner, B.M.5    Eisenman, R.N.6    Bird, A.7
  • 21
    • 0346993510 scopus 로고    scopus 로고
    • Direct association between PU.1 and MeCP2 that recruits mSin3A-HDAC complex for PU. 1-mediated transcriptional repression
    • Suzuki, M., Yamada, T., Kihara-Negishi, F., Sakurai, T. and Oikawa, T. (2003) Direct association between PU.1 and MeCP2 that recruits mSin3A-HDAC complex for PU.1-mediated transcriptional repression. Oncogene, 22, 8688-8698.
    • (2003) Oncogene , vol.22 , pp. 8688-8698
    • Suzuki, M.1    Yamada, T.2    Kihara-Negishi, F.3    Sakurai, T.4    Oikawa, T.5
  • 22
    • 0043178993 scopus 로고    scopus 로고
    • A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos
    • Stancheva, I., Collins, A.L., Van den Veyver, I.B., Zoghbi, H. and Meehan, R.R. (2003) A mutant form of MeCP2 protein associated with human Rett syndrome cannot be displaced from methylated DNA by notch in Xenopus embryos. Mol. Cell, 12, 425-435.
    • (2003) Mol. Cell , vol.12 , pp. 425-435
    • Stancheva, I.1    Collins, A.L.2    Van den Veyver, I.B.3    Zoghbi, H.4    Meehan, R.R.5
  • 23
    • 0037423186 scopus 로고    scopus 로고
    • The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation
    • Fuks, F., Hurd, P.J., Wolf, D., Nan, X., Bird, A.P. and Kouzarides, T. (2003) The methyl-CpG-binding protein MeCP2 links DNA methylation to histone methylation. J. Biol. Chem., 278, 4035-4040.
    • (2003) J. Biol. Chem. , vol.278 , pp. 4035-4040
    • Fuks, F.1    Hurd, P.J.2    Wolf, D.3    Nan, X.4    Bird, A.P.5    Kouzarides, T.6
  • 24
    • 0038136913 scopus 로고    scopus 로고
    • Methyl-CpG-binding protein, MeCP2, is a target molecule for maintenance DNA methyltransferase
    • Kimura, H. and Shiota, K. (2003) Methyl-CpG-binding protein, MeCP2, is a target molecule for maintenance DNA methyltransferase, Dnmt1. J. Biol. Chem., 278, 4806-4812.
    • (2003) Dnmt1. J. Biol. Chem. , vol.278 , pp. 4806-4812
    • Kimura, H.1    Shiota, K.2
  • 27
    • 45849105557 scopus 로고    scopus 로고
    • MeCP2, a key contributor to neurological disease, activates and represses transcription
    • Chahrour, M., Jung, S.Y., Shaw, C., Zhou, X., Wong, S.T., Qin, J. and Zoghbi, H.Y. (2008) MeCP2, a key contributor to neurological disease, activates and represses transcription. Science, 320, 1224-1229.
    • (2008) Science , vol.320 , pp. 1224-1229
    • Chahrour, M.1    Jung, S.Y.2    Shaw, C.3    Zhou, X.4    Wong, S.T.5    Qin, J.6    Zoghbi, H.Y.7
  • 29
    • 10744222511 scopus 로고    scopus 로고
    • A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome
    • Buschdorf, J.P. and Stratling, W.H. (2004) A WW domain binding region in methyl-CpG-binding protein MeCP2: impact on Rett syndrome. J. Mol. Med., 82, 135-143.
    • (2004) J. Mol. Med. , vol.82 , pp. 135-143
    • Buschdorf, J.P.1    Stratling, W.H.2
  • 31
    • 0242300612 scopus 로고    scopus 로고
    • DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation
    • Martinowich, K., Hattori, D., Wu, H., Fouse, S., He, F., Hu, Y., Fan, G. and Sun, Y.E. (2003) DNA methylation-related chromatin remodeling in activity-dependent BDNF gene regulation. Science, 302, 890-893.
    • (2003) Science , vol.302 , pp. 890-893
    • Martinowich, K.1    Hattori, D.2    Wu, H.3    Fouse, S.4    He, F.5    Hu, Y.6    Fan, G.7    Sun, Y.E.8
  • 32
    • 33749590330 scopus 로고    scopus 로고
    • Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation
    • Zhou, Z., Hong, E.J., Cohen, S., Zhao, W.N., Ho, H.Y., Schmidt, L., Chen, W.G., Lin, Y., Savner, E., Griffith, E.C. et al. (2006) Brain-specific phosphorylation of MeCP2 regulates activity-dependent Bdnf transcription, dendritic growth, and spine maturation. Neuron, 52, 255-269.
    • (2006) Neuron , vol.52 , pp. 255-269
    • Zhou, Z.1    Hong, E.J.2    Cohen, S.3    Zhao, W.N.4    Ho, H.Y.5    Schmidt, L.6    Chen, W.G.7    Lin, Y.8    Savner, E.9    Griffith, E.C.10
  • 33
    • 33845332685 scopus 로고    scopus 로고
    • Phosphorylation of methyl-CpG binding protein 2 (MeCP2) regulates the intracellular localization during neuronal cell differentiation
    • Miyake, K. and Nagai, K. (2007) Phosphorylation of methyl-CpG binding protein 2 (MeCP2) regulates the intracellular localization during neuronal cell differentiation. Neurochem. Int., 50, 264-270.
    • (2007) Neurochem. Int. , vol.50 , pp. 264-270
    • Miyake, K.1    Nagai, K.2
  • 34
    • 28744458248 scopus 로고    scopus 로고
    • A segment of the Mecp2 promoter is sufficient to drive expression in neurons
    • Adachi, M., Keefer, E.W. and Jones, F.S. (2005) A segment of the Mecp2 promoter is sufficient to drive expression in neurons. Hum. Mol. Genet., 14, 3709-3722.
    • (2005) Hum. Mol. Genet. , vol.14 , pp. 3709-3722
    • Adachi, M.1    Keefer, E.W.2    Jones, F.S.3
  • 36
    • 0037081840 scopus 로고    scopus 로고
    • Insight into Rett syndrome: MeCP2 levels display tissueand cell-specific differences and correlate with neuronal maturation
    • Shahbazian, M.D., Antalffy, B., Armstrong, D.L. and Zoghbi, H.Y. (2002) Insight into Rett syndrome: MeCP2 levels display tissueand cell-specific differences and correlate with neuronal maturation. Hum. Mol. Genet., 11, 115-124.
    • (2002) Hum. Mol. Genet. , vol.11 , pp. 115-124
    • Shahbazian, M.D.1    Antalffy, B.2    Armstrong, D.L.3    Zoghbi, H.Y.4
  • 37
    • 0030188404 scopus 로고    scopus 로고
    • Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2
    • D'Esposito, M., Quaderi, N.A., Ciccodicola, A., Bruni, P., Esposito, T., D'Urso, M. and Brown, S.D. (1996) Isolation, physical mapping, and northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2. Mamm. Genome, 7, 533-535.
    • (1996) Mamm. Genome , vol.7 , pp. 533-535
    • D'Esposito, M.1    Quaderi, N.A.2    Ciccodicola, A.3    Bruni, P.4    Esposito, T.5    D'Urso, M.6    Brown, S.D.7
  • 38
    • 0032776138 scopus 로고    scopus 로고
    • A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3′-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression
    • Coy, J.F., Sedlacek, Z., Bachner, D., Delius, H. and Poustka, A. (1999) A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3′-untranslated region of the methyl-CpG-binding protein 2 gene (MeCP2) suggests a regulatory role in gene expression. Hum. Mol. Genet., 8, 1253-1262.
    • (1999) Hum. Mol. Genet. , vol.8 , pp. 1253-1262
    • Coy, J.F.1    Sedlacek, Z.2    Bachner, D.3    Delius, H.4    Poustka, A.5
  • 40
    • 2542481314 scopus 로고    scopus 로고
    • The major form of MeCP2 has a novel N-terminus generated by alternative splicing
    • Kriaucionis, S. and Bird, A. (2004) The major form of MeCP2 has a novel N-terminus generated by alternative splicing. Nucleic Acids Res., 32, 1818-1823.
    • (2004) Nucleic Acids Res. , vol.32 , pp. 1818-1823
    • Kriaucionis, S.1    Bird, A.2
  • 41
    • 34247197220 scopus 로고    scopus 로고
    • Differential distribution of the MeCP2 splice variants in the postnatal mouse brain
    • Dragich, J.M., Kim, Y.H., Arnold, A.P. and Schanen, N.C. (2007) Differential distribution of the MeCP2 splice variants in the postnatal mouse brain. J. Comp. Neurol., 501, 526-542.
    • (2007) J. Comp. Neurol. , vol.501 , pp. 526-542
    • Dragich, J.M.1    Kim, Y.H.2    Arnold, A.P.3    Schanen, N.C.4
  • 42
    • 66849106361 scopus 로고    scopus 로고
    • Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation
    • Parmeggiani, A., Tedde, M.R., Arbizzani, A., Posar, A., Scaduto, M.C., Santucci, M. and Sangiorgi, S. (2009) Methyl-CpG-binding protein 2 (MECP2) gene mutations in an Italian sample of patients with pervasive developmental disorder and mental retardation. J. Child Neurol., 24, 772-774.
    • (2009) J. Child Neurol. , vol.24 , pp. 772-774
    • Parmeggiani, A.1    Tedde, M.R.2    Arbizzani, A.3    Posar, A.4    Scaduto, M.C.5    Santucci, M.6    Sangiorgi, S.7
  • 43
    • 34447297311 scopus 로고    scopus 로고
    • MECP2 mutations in males
    • Villard, L. (2007) MECP2 mutations in males. J. Med. Genet., 44, 417-423.
    • (2007) J. Med. Genet. , vol.44 , pp. 417-423
    • Villard, L.1
  • 44
    • 58049116929 scopus 로고    scopus 로고
    • A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype
    • Adegbola, A.A., Gonzales, M.L., Chess, A., Lasalle, J.M. and Cox, G.F. (2009) A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype. Hum. Genet., 124, 615-623.
    • (2009) Hum. Genet. , vol.124 , pp. 615-623
    • Adegbola, A.A.1    Gonzales, M.L.2    Chess, A.3    Lasalle, J.M.4    Cox, G.F.5
  • 47
    • 60549103074 scopus 로고    scopus 로고
    • The clinical variability of the MECP2 duplication syndrome: description of two families with duplications excluding L1CAM and FLNA
    • Kirk, E.P., Malaty-Brevaud, V., Martini, N., Lacoste, C., Levy, N., Maclean, K., Davies, L., Philip, N. and Badens, C. (2009) The clinical variability of the MECP2 duplication syndrome: description of two families with duplications excluding L1CAM and FLNA. Clin. Genet., 75, 301-303.
    • (2009) Clin. Genet. , vol.75 , pp. 301-303
    • Kirk, E.P.1    Malaty-Brevaud, V.2    Martini, N.3    Lacoste, C.4    Levy, N.5    Maclean, K.6    Davies, L.7    Philip, N.8    Badens, C.9
  • 55
    • 67649416452 scopus 로고    scopus 로고
    • Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome
    • O'Connor, R.D., Zayzafoon, M., Farach-Carson, M.C. and Schanen, N.C. (2009) Mecp2 deficiency decreases bone formation and reduces bone volume in a rodent model of Rett syndrome. Bone, 45, 346-356.
    • (2009) Bone , vol.45 , pp. 346-356
    • O'Connor, R.D.1    Zayzafoon, M.2    Farach-Carson, M.C.3    Schanen, N.C.4
  • 58
    • 23944509593 scopus 로고    scopus 로고
    • Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome
    • Meins, M., Lehmann, J., Gerresheim, F., Herchenbach, J., Hagedorn, M., Hameister, K. and Epplen, J.T. (2005) Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndrome. J. Med. Genet., 42, e12.
    • (2005) J. Med. Genet. , vol.42
    • Meins, M.1    Lehmann, J.2    Gerresheim, F.3    Herchenbach, J.4    Hagedorn, M.5    Hameister, K.6    Epplen, J.T.7
  • 59
    • 34548715822 scopus 로고    scopus 로고
    • Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis
    • Alvarez-Saavedra, M., Saez, M.A., Kang, D., Zoghbi, H.Y. and Young, J.I. (2007) Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis. Hum. Mol. Genet., 16, 2315-2325.
    • (2007) Hum. Mol. Genet. , vol.16 , pp. 2315-2325
    • Alvarez-Saavedra, M.1    Saez, M.A.2    Kang, D.3    Zoghbi, H.Y.4    Young, J.I.5
  • 61
    • 3042615163 scopus 로고    scopus 로고
    • Embryonic stem cells and mice expressing different GFP variants for multiple non-invasive reporter usage within a single animal
    • Hadjantonakis, A.K., Macmaster, S. and Nagy, A. (2002) Embryonic stem cells and mice expressing different GFP variants for multiple non-invasive reporter usage within a single animal. BMC Biotechnol., 2, 11.
    • (2002) BMC Biotechnol. , vol.2 , pp. 11
    • Hadjantonakis, A.K.1    Macmaster, S.2    Nagy, A.3
  • 62
    • 0035894949 scopus 로고    scopus 로고
    • Observation of antigen-dependent CD8+ T-cell/dendritic cell interactions in vivo
    • Schaefer, B.C., Schaefer, M.L., Kappler, J.W., Marrack, P. and Kedl, R.M. (2001) Observation of antigen-dependent CD8+ T-cell/dendritic cell interactions in vivo. Cell Immunol., 214, 110-122.
    • (2001) Cell Immunol. , vol.214 , pp. 110-122
    • Schaefer, B.C.1    Schaefer, M.L.2    Kappler, J.W.3    Marrack, P.4    Kedl, R.M.5
  • 63
    • 0032143165 scopus 로고    scopus 로고
    • Generating green fluorescent mice by germline transmission of green fluorescent ES cells
    • Hadjantonakis, A.K., Gertsenstein, M., Ikawa, M., Okabe, M. and Nagy, A. (1998) Generating green fluorescent mice by germline transmission of green fluorescent ES cells. Mech. Dev., 76, 79-90.
    • (1998) Mech. Dev. , vol.76 , pp. 79-90
    • Hadjantonakis, A.K.1    Gertsenstein, M.2    Ikawa, M.3    Okabe, M.4    Nagy, A.5
  • 64
    • 0034488835 scopus 로고    scopus 로고
    • Z/EG, a double reporter mouse line that expresses enhanced green fluorescent protein upon Cre-mediated excision
    • Novak, A., Guo, C., Yang, W., Nagy, A. and Lobe, C.G. (2000) Z/EG, a double reporter mouse line that expresses enhanced green fluorescent protein upon Cre-mediated excision. Genesis, 28, 147-155.
    • (2000) Genesis , vol.28 , pp. 147-155
    • Novak, A.1    Guo, C.2    Yang, W.3    Nagy, A.4    Lobe, C.G.5
  • 65
    • 0033373398 scopus 로고    scopus 로고
    • The green fluorescent protein is an efficient biological marker for cardiac myocytes
    • Xian, M., Honbo, N., Zhang, J., Liew, C.C., Karliner, J.S. and Lau, Y.F. (1999) The green fluorescent protein is an efficient biological marker for cardiac myocytes. J. Mol. Cell Cardiol., 31, 2155-2165.
    • (1999) J. Mol. Cell Cardiol. , vol.31 , pp. 2155-2165
    • Xian, M.1    Honbo, N.2    Zhang, J.3    Liew, C.C.4    Karliner, J.S.5    Lau, Y.F.6
  • 66
    • 0034106175 scopus 로고    scopus 로고
    • Transgenic expression of green fluorescence protein can cause dilated cardiomyopathy
    • Huang, W.Y., Aramburu, J., Douglas, P.S. and Izumo, S. (2000) Transgenic expression of green fluorescence protein can cause dilated cardiomyopathy. Nat. Med., 6, 482-483.
    • (2000) Nat. Med. , vol.6 , pp. 482-483
    • Huang, W.Y.1    Aramburu, J.2    Douglas, P.S.3    Izumo, S.4
  • 68
    • 0346098146 scopus 로고    scopus 로고
    • Impact of embryonic expression of enhanced green fluorescent protein on early mouse development
    • Devgan, V., Rao, M.R. and Seshagiri, P.B. (2004) Impact of embryonic expression of enhanced green fluorescent protein on early mouse development. Biochem. Biophys. Res. Commun., 313, 1030-1036.
    • (2004) Biochem. Biophys. Res. Commun. , vol.313 , pp. 1030-1036
    • Devgan, V.1    Rao, M.R.2    Seshagiri, P.B.3
  • 69
    • 0025063668 scopus 로고
    • Transgenic mice expressing beta-galactosidase in mature neurons under neuron-specific enolase promoter control
    • Forss-Petter, S., Danielson, P.E., Catsicas, S., Battenberg, E., Price, J., Nerenberg, M. and Sutcliffe, J.G. (1990) Transgenic mice expressing beta-galactosidase in mature neurons under neuron-specific enolase promoter control. Neuron, 5, 187-197.
    • (1990) Neuron , vol.5 , pp. 187-197
    • Forss-Petter, S.1    Danielson, P.E.2    Catsicas, S.3    Battenberg, E.4    Price, J.5    Nerenberg, M.6    Sutcliffe, J.G.7
  • 72
    • 0035936792 scopus 로고    scopus 로고
    • The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms
    • Seidman, J.G. and Seidman, C. (2001) The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell, 104, 557-567.
    • (2001) Cell , vol.104 , pp. 557-567
    • Seidman, J.G.1    Seidman, C.2
  • 73
    • 15244351322 scopus 로고    scopus 로고
    • ′-UTR in the brain and visceral organs during mouse development
    • Pelka, G.J., Watson, C.M., Christodoulou, J. and Tam, P.P. (2005) Distinct expression profiles of Mecp2 transcripts with different lengths of 3′-UTR in the brain and visceral organs during mouse development. Genomics, 85, 441-452.
    • (2005) Genomics , vol.85 , pp. 441-452
    • Pelka, G.J.1    Watson, C.M.2    Christodoulou, J.3    Tam, P.P.4
  • 81
    • 34548550547 scopus 로고    scopus 로고
    • Autonomic cardiovascular control in methyl-CpG-binding protein 2 (Mecp2) deficient mice
    • Bissonnette, J.M., Knopp, S.J., Maylie, J. and Thong, T. (2007) Autonomic cardiovascular control in methyl-CpG-binding protein 2 (Mecp2) deficient mice. Auton. Neurosci., 136, 82-89.
    • (2007) Auton. Neurosci. , vol.136 , pp. 82-89
    • Bissonnette, J.M.1    Knopp, S.J.2    Maylie, J.3    Thong, T.4
  • 82
    • 0028235383 scopus 로고
    • Electrocardiographic findings in Rett syndrome: an explanation for sudden death?
    • Sekul, E.A., Moak, J.P., Schultz, R.J., Glaze, D.G., Dunn, J.K. and Percy, A.K. (1994) Electrocardiographic findings in Rett syndrome: an explanation for sudden death? J. Pediatr., 125, 80-82.
    • (1994) J. Pediatr , vol.125 , pp. 80-82
    • Sekul, E.A.1    Moak, J.P.2    Schultz, R.J.3    Glaze, D.G.4    Dunn, J.K.5    Percy, A.K.6
  • 84
    • 0028969127 scopus 로고
    • Electrocardiographic findings in Rett syndrome
    • Fuster-Siebert, M. and Castro-Gago, M. (1995) Electrocardiographic findings in Rett syndrome. J. Pediatr., 126, 506.
    • (1995) J. Pediatr. , vol.126 , pp. 506
    • Fuster-Siebert, M.1    Castro-Gago, M.2
  • 85
    • 0032764776 scopus 로고    scopus 로고
    • Reduced heart rate variability in patients affected with Rett syndrome. A possible explanation for sudden death
    • Guideri, F., Acampa, M., Hayek, G., Zappella, M. and Di, P.T. (1999) Reduced heart rate variability in patients affected with Rett syndrome. A possible explanation for sudden death. Neuropediatrics, 30, 146-148.
    • (1999) Neuropediatrics , vol.30 , pp. 146-148
    • Guideri, F.1    Acampa, M.2    Hayek, G.3    Zappella, M.4    Di, P.T.5
  • 86
    • 33646377640 scopus 로고    scopus 로고
    • Cardiac disease and Rett syndrome
    • Acampa, M. and Guideri, F. (2006) Cardiac disease and Rett syndrome. Arch. Dis. Child, 91, 440-443.
    • (2006) Arch. Dis. Child , vol.91 , pp. 440-443
    • Acampa, M.1    Guideri, F.2
  • 87
    • 27144484259 scopus 로고    scopus 로고
    • Neurophysiology of Rett syndrome
    • Glaze, D.G. (2005) Neurophysiology of Rett syndrome. J. Child Neurol., 20, 740-746.
    • (2005) J. Child Neurol. , vol.20 , pp. 740-746
    • Glaze, D.G.1
  • 88
    • 0034970104 scopus 로고    scopus 로고
    • Progressive cardiac dysautonomia observed in patients affected by classic Rett syndrome and not in the preserved speech variant
    • Guideri, F., Acampa, M., DiPerri, T., Zappella, M. and Hayek, Y. (2001) Progressive cardiac dysautonomia observed in patients affected by classic Rett syndrome and not in the preserved speech variant. J. Child Neurol., 16, 370-373.
    • (2001) J. Child Neurol. , vol.16 , pp. 370-373
    • Guideri, F.1    Acampa, M.2    DiPerri, T.3    Zappella, M.4    Hayek, Y.5
  • 89
    • 0242456117 scopus 로고    scopus 로고
    • Possible mechanisms of osteopenia in Rett syndrome: bone histomorphometric studies
    • Budden, S.S. and Gunness, M.E. (2003) Possible mechanisms of osteopenia in Rett syndrome: bone histomorphometric studies. J. Child Neurol., 18, 698-702.
    • (2003) J. Child Neurol. , vol.18 , pp. 698-702
    • Budden, S.S.1    Gunness, M.E.2
  • 90
    • 33845992511 scopus 로고    scopus 로고
    • Methylation status of a single CpG locus 3 bases upstream of TATA-box of receptor activator of nuclear factor-kappaB ligand (RANKL) gene promoter modulates cell-and tissue-specific RANKL expression and osteoclastogenesis
    • Kitazawa, R. and Kitazawa, S. (2007) Methylation status of a single CpG locus 3 bases upstream of TATA-box of receptor activator of nuclear factor-kappaB ligand (RANKL) gene promoter modulates cell-and tissue-specific RANKL expression and osteoclastogenesis. Mol. Endocrinol., 21, 148-158.
    • (2007) Mol. Endocrinol. , vol.21 , pp. 148-158
    • Kitazawa, R.1    Kitazawa, S.2
  • 91
    • 0030684749 scopus 로고    scopus 로고
    • Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts
    • Komori, T., Yagi, H., Nomura, S., Yamaguchi, A., Sasaki, K., Deguchi, K., Shimizu, Y., Bronson, R.T., Gao, Y.H., Inada, M. et al. (1997) Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts. Cell, 89, 755-764.
    • (1997) Cell , vol.89 , pp. 755-764
    • Komori, T.1    Yagi, H.2    Nomura, S.3    Yamaguchi, A.4    Sasaki, K.5    Deguchi, K.6    Shimizu, Y.7    Bronson, R.T.8    Gao, Y.H.9    Inada, M.10
  • 95
    • 0030927622 scopus 로고    scopus 로고
    • Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia
    • Lee, B., Thirunavukkarasu, K., Zhou, L., Pastore, L., Baldini, A., Hecht, J., Geoffroy, V., Ducy, P. and Karsenty, G. (1997) Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. Nat. Genet., 16, 307-310.
    • (1997) Nat. Genet. , vol.16 , pp. 307-310
    • Lee, B.1    Thirunavukkarasu, K.2    Zhou, L.3    Pastore, L.4    Baldini, A.5    Hecht, J.6    Geoffroy, V.7    Ducy, P.8    Karsenty, G.9
  • 96
    • 0036186852 scopus 로고    scopus 로고
    • Mutations in the RUNX2 gene in patients with cleidocranial dysplasia
    • Otto, F., Kanegane, H. and Mundlos, S. (2002) Mutations in the RUNX2 gene in patients with cleidocranial dysplasia. Hum. Mutat., 19, 209-216.
    • (2002) Hum. Mutat. , vol.19 , pp. 209-216
    • Otto, F.1    Kanegane, H.2    Mundlos, S.3
  • 97
    • 0037624892 scopus 로고    scopus 로고
    • Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype-phenotype correlations
    • Yoshida, T., Kanegane, H., Osato, M., Yanagida, M., Miyawaki, T., Ito, Y. and Shigesada, K. (2003) Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype-phenotype correlations. Blood Cells Mol. Dis., 30, 184-193.
    • (2003) Blood Cells Mol. Dis. , vol.30 , pp. 184-193
    • Yoshida, T.1    Kanegane, H.2    Osato, M.3    Yanagida, M.4    Miyawaki, T.5    Ito, Y.6    Shigesada, K.7
  • 99


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.