The Conundrum Posed by Cellular Heterogeneity in Analysis of Human Neuroblastoma
200, Department of Biological Sciences, Fordham University, 441 E. FordhamRd., Bronx, NY 10458 (e-mail: rross@fordham.edu).DOI: 10.1093/jnci/djh262Journal of the National Cancer Institute, Vol. 96, No. 16, Oxford UniversityPress 2004, all rights reserved.1192 EDITORIALS Journal of the National Cance...
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description | 200, Department of Biological Sciences, Fordham University, 441 E. FordhamRd., Bronx, NY 10458 (e-mail: rross@fordham.edu).DOI: 10.1093/jnci/djh262Journal of the National Cancer Institute, Vol. 96, No. 16, Oxford UniversityPress 2004, all rights reserved.1192 EDITORIALS Journal of the National Cancer Institute, Vol. 96, No. 16, August 18, 2004(caspase-8, FLIP, DcR1, DcR2, DR4, and DR5) were hypermethylated in the majority of cell lines. In tumors, only the loss of |
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In tumors, only the loss of</description><identifier>ISSN: 0027-8874</identifier><identifier>EISSN: 1460-2105</identifier><identifier>DOI: 10.1093/jnci/djh262</identifier><identifier>PMID: 15316046</identifier><identifier>CODEN: JNCIEQ</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Cell Line, Tumor ; Clone Cells ; Cluster Analysis ; DNA Methylation ; DNA, Neoplasm - metabolism ; Gene Amplification ; Gene Expression Regulation, Neoplastic ; Gene Silencing ; Humans ; Multigene Family ; N-Myc Proto-Oncogene Protein ; Neuroblastoma - genetics ; Nuclear Proteins - genetics ; Oncogene Proteins - genetics ; Promoter Regions, Genetic</subject><ispartof>JNCI : Journal of the National Cancer Institute, 2004-08, Vol.96 (16), p.1192-1193</ispartof><rights>Copyright Oxford University Press(England) Aug 18, 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-423fd68964ad162c35c74ebbdf4a7cef180e6314a130d1c79f5a1f9072f589723</citedby><cites>FETCH-LOGICAL-c387t-423fd68964ad162c35c74ebbdf4a7cef180e6314a130d1c79f5a1f9072f589723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15316046$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ross, Robert A.</creatorcontrib><creatorcontrib>Spengler, Barbara A.</creatorcontrib><title>The Conundrum Posed by Cellular Heterogeneity in Analysis of Human Neuroblastoma</title><title>JNCI : Journal of the National Cancer Institute</title><addtitle>JNCI J Natl Cancer Inst</addtitle><description>200, Department of Biological Sciences, Fordham University, 441 E. 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subjects | Cell Line, Tumor Clone Cells Cluster Analysis DNA Methylation DNA, Neoplasm - metabolism Gene Amplification Gene Expression Regulation, Neoplastic Gene Silencing Humans Multigene Family N-Myc Proto-Oncogene Protein Neuroblastoma - genetics Nuclear Proteins - genetics Oncogene Proteins - genetics Promoter Regions, Genetic |
title | The Conundrum Posed by Cellular Heterogeneity in Analysis of Human Neuroblastoma |
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