rdf:type |
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lifeskim:mentions |
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pubmed:dateCreated |
2008-5-9
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pubmed:abstractText |
Esophageal squamous cell carcinoma (ESCC) is a genetically complex tumor type and a major cause of cancer related mortality. Although distinct genetic alterations have been linked to ESCC development and prognosis, the genetic alterations have not gained clinical applicability. We applied array-based comparative genomic hybridization (aCGH) to obtain a whole genome copy number profile relevant for identifying deranged pathways and clinically applicable markers.
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:issn |
1471-2407
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pubmed:author |
|
pubmed:issnType |
Electronic
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
98
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:18405350-Aged,
pubmed-meshheading:18405350-Esophageal Neoplasms,
pubmed-meshheading:18405350-Female,
pubmed-meshheading:18405350-Genetic Markers,
pubmed-meshheading:18405350-Humans,
pubmed-meshheading:18405350-Male,
pubmed-meshheading:18405350-Middle Aged,
pubmed-meshheading:18405350-Neoplasms, Squamous Cell,
pubmed-meshheading:18405350-Nucleic Acid Hybridization,
pubmed-meshheading:18405350-Prognosis
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pubmed:year |
2008
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pubmed:articleTitle |
Prognostic impact of array-based genomic profiles in esophageal squamous cell cancer.
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pubmed:affiliation |
Department of Oncology, Lund University Hospital, 221 85 Lund, Sweden. Ana.Carneiro@med.lu.se
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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