Source:http://linkedlifedata.com/resource/pubmed/id/11325887
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2001-4-30
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pubmed:abstractText |
Molecular detection methods for HER2/neu gene amplification include fluorescence in situ hybridization (FISH) and competitive PCR. We designed a quantitative PCR system utilizing fluorescent hybridization probes and a competitor that differed from the HER2/neu sequence by a single base change.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0009-9147
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
47
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
844-51
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11325887-DNA,
pubmed-meshheading:11325887-Fluorescent Dyes,
pubmed-meshheading:11325887-Gene Dosage,
pubmed-meshheading:11325887-Genes, erbB-2,
pubmed-meshheading:11325887-Humans,
pubmed-meshheading:11325887-In Situ Hybridization, Fluorescence,
pubmed-meshheading:11325887-Polymerase Chain Reaction,
pubmed-meshheading:11325887-Tumor Cells, Cultured
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pubmed:year |
2001
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pubmed:articleTitle |
Quantification of HER2/neu gene amplification by competitive pcr using fluorescent melting curve analysis.
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pubmed:affiliation |
Department of Pathology, School of Medicine, University of Utah, Salt Lake 84132, USA. lyone@aruolab.com
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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