{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,5,8]],"date-time":"2024-05-08T00:08:09Z","timestamp":1715126889125},"reference-count":34,"publisher":"Editorial Committee of Japanese Journal of Infectious Diseases, National Institute of Infectious Dis","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Jpn J Infect Dis"],"published-print":{"date-parts":[[2013]]},"DOI":"10.7883\/yoken.66.126","type":"journal-article","created":{"date-parts":[[2013,3,21]],"date-time":"2013-03-21T01:35:44Z","timestamp":1363829744000},"page":"126-132","source":"Crossref","is-referenced-by-count":1,"title":["Relationship between Methyl CpG Binding Protein 2 and JC Viral Proteins"],"prefix":"10.7883","volume":"66","author":[{"given":"Kenta","family":"Takahashi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasuko","family":"Orba","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Taichi","family":"Kimura","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lei","family":"Wang","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shinji","family":"Kohsaka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Masumi","family":"Tsuda","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mishie","family":"Tanino","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hiroshi","family":"Nishihara","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kazuo","family":"Nagashima","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Hirofumi","family":"Sawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shinya","family":"Tanaka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"4631","reference":[{"key":"1","unstructured":"1. Koralnik, I.J., Schellingerhout, D. and Frosch, M.P. (2004): Case records of the Massachusetts General Hospital. Weekly clinicopathological exercises. Case 14&ndash;2004. A 66-year-old man with progressive neurologic deficits. N. Engl. J. Med., 350, 1882&ndash;1893."},{"key":"2","doi-asserted-by":"publisher","DOI":"10.1016\/S1474-4422(10)70040-5"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3. Berger, J.R. (2007): Progressive multifocal leukoencephalopathy. Curr. Neurol. Neurosci. Rep., 7, 461&ndash;469.","DOI":"10.1016\/S0072-9752(07)85013-5"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Wuthrich, C., Dang, X., Westmoreland, S., et al. (2009): Fulminant JC virus encephalopathy with productive infection of cortical pyramidal neurons. Ann. Neurol., 65, 742&ndash;748.","DOI":"10.1002\/ana.21619"},{"key":"5","doi-asserted-by":"publisher","DOI":"10.1002\/ana.20431"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6. Frisque, R.J., Bream, G.L. and Cannella, M.T. (1984): Human polyomavirus JC virus genome. J. Virol., 51, 458&ndash;469.","DOI":"10.1128\/JVI.51.2.458-469.1984"},{"key":"7","doi-asserted-by":"crossref","unstructured":"8. Suzuki, T., Orba, Y., Okada, Y., et al. (2010): The human polyoma JC virus agnoprotein acts as a viroporin. PLoS Pathog., 6, e1000801.","DOI":"10.1371\/journal.ppat.1000801"},{"key":"8","doi-asserted-by":"publisher","DOI":"10.1016\/0092-8674(92)90610-O"},{"key":"9","doi-asserted-by":"publisher","DOI":"10.1016\/S0092-8674(00)81887-5"},{"key":"10","doi-asserted-by":"publisher","DOI":"10.1038\/30764"},{"key":"11","doi-asserted-by":"crossref","unstructured":"13. Yasui, D.H., Peddada, S., Bieda, M.C., et al. (2007): Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proc. Natl. Acad. Sci. USA, 104, 19416&ndash;19421.","DOI":"10.1073\/pnas.0707442104"},{"key":"12","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.M305308200"},{"key":"13","doi-asserted-by":"crossref","unstructured":"16. Horike, S., Cai, S., Miyano, M., et al. (2005): Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome. Nat. Genet., 37, 31&ndash;40.","DOI":"10.1038\/ng1491"},{"key":"14","doi-asserted-by":"publisher","DOI":"10.1139\/O08-115"},{"key":"15","doi-asserted-by":"publisher","DOI":"10.1038\/13810"},{"key":"16","doi-asserted-by":"publisher","DOI":"10.1086\/444549"},{"key":"17","doi-asserted-by":"crossref","unstructured":"21. Samaco, R.C., Nagarajan, R.P., Braunschweig, D. et al. (2004): Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders. Hum. Mol. Genet., 13, 629&ndash;639.","DOI":"10.1093\/hmg\/ddh063"},{"key":"18","doi-asserted-by":"crossref","unstructured":"22. Collins, A.L., Levenson, J.M., Vilaythong, A.P., et al. (2004): Mild overexpression of MeCP2 causes a progressive neurological disorder in mice. Hum. Mol. Genet., 13, 2679&ndash;2689.","DOI":"10.1093\/hmg\/ddh282"},{"key":"19","doi-asserted-by":"crossref","unstructured":"28. Momozaki, N., Oh-Uchida, M., Tabuchi, K., et al. (1992): Suppression of anchorage-independent growth of human glioblastoma cell by major histocompatibility complex class I gene-transfection. J. Neurosurg., 76, 845&ndash;849.","DOI":"10.3171\/jns.1992.76.5.0845"},{"key":"20","doi-asserted-by":"publisher","DOI":"10.1128\/JVI.77.2.1347-1356.2003"},{"key":"21","doi-asserted-by":"publisher","DOI":"10.1074\/jbc.M002324200"},{"key":"22","doi-asserted-by":"crossref","unstructured":"31. Sunden, Y., Suzuki, T., Orba, Y., et al. (2006): Characterization and application of polyclonal antibodies that specifically recognize JC virus large T antigen. Acta Neuropathol., 111, 379&ndash;387.","DOI":"10.1007\/s00401-005-0025-9"},{"key":"23","doi-asserted-by":"crossref","unstructured":"32. Kudo, S., Nomura, Y., Segawa, M., et al. (2001): Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems. Brain Dev., 23 (Suppl 1), S165&ndash;173.","DOI":"10.1016\/S0387-7604(01)00345-X"},{"key":"24","doi-asserted-by":"crossref","unstructured":"33. Kudo, S., Nomura, Y., Segawa, M., et al. (2003): Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain. J. Med. Genet., 40, 487&ndash;493.","DOI":"10.1136\/jmg.40.7.487"},{"key":"25","doi-asserted-by":"crossref","unstructured":"34. Liu, J. and Francke, U. (2006): Identification of <i>cis<\/i>-regulatory elements for <i>MECP2<\/i> expression. Hum. Mol. Genet., 15, 1769&ndash;1782.","DOI":"10.1093\/hmg\/ddl099"},{"key":"26","doi-asserted-by":"crossref","unstructured":"35. Kudo, S. (1998): Methyl-CpG-binding protein MeCP2 represses Sp1-activated transcription of the human leukosialin gene when the promoter is methylated. Mol. Cell. Biol., 18, 5492&ndash;5499.","DOI":"10.1128\/MCB.18.9.5492"},{"key":"27","doi-asserted-by":"publisher","DOI":"10.1007\/s00401-002-0526-8"},{"key":"28","doi-asserted-by":"publisher","DOI":"10.1006\/viro.2001.0972"},{"key":"29","doi-asserted-by":"publisher","DOI":"10.1128\/JVI.78.13.7270-7273.2004"},{"key":"30","doi-asserted-by":"publisher","DOI":"10.1128\/JVI.76.22.11596-11604.2002"},{"key":"31","unstructured":"45. Takaoka, N., Takayama, T., Teratani, T., et al. (2011): Analysis of the regulation of fatty acid binding protein 7 expression in human renal carcinoma cell lines. BMC Mol. Biol., 12, 31."},{"key":"32","doi-asserted-by":"publisher","DOI":"10.1016\/j.cell.2009.01.002"},{"key":"33","doi-asserted-by":"crossref","unstructured":"47. Nagarajan, R., Hogart, A., Gwye, Y., et al. (2006): Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant <i>MECP2<\/i> promoter methylation. Epigenetics, 1, 172&ndash;182.","DOI":"10.4161\/epi.1.4.3514"},{"key":"34","doi-asserted-by":"crossref","unstructured":"48. Nagarajan, R.P., Patzel, K.A., Martin, M., et al. (2008): <i>MECP2<\/i> promoter methylation and X chromosome inactivation in autism. Autism Res., 1, 169&ndash;178.","DOI":"10.1002\/aur.24"}],"container-title":["Japanese Journal of Infectious Diseases"],"original-title":[],"language":"en","deposited":{"date-parts":[[2024,5,7]],"date-time":"2024-05-07T19:12:24Z","timestamp":1715109144000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.jstage.jst.go.jp\/article\/yoken\/66\/2\/66_126\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013]]},"references-count":34,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2013]]}},"URL":"https:\/\/doi.org\/10.7883\/yoken.66.126","relation":{},"ISSN":["1344-6304"],"issn-type":[{"value":"1344-6304","type":"print"}],"subject":[],"published":{"date-parts":[[2013]]}}}