pubmed-article:17764544 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17764544 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:17764544 | lifeskim:mentions | umls-concept:C0079419 | lld:lifeskim |
pubmed-article:17764544 | lifeskim:mentions | umls-concept:C0015295 | lld:lifeskim |
pubmed-article:17764544 | lifeskim:mentions | umls-concept:C1719039 | lld:lifeskim |
pubmed-article:17764544 | lifeskim:mentions | umls-concept:C0599882 | lld:lifeskim |
pubmed-article:17764544 | lifeskim:mentions | umls-concept:C0441633 | lld:lifeskim |
pubmed-article:17764544 | pubmed:dateCreated | 2007-10-16 | lld:pubmed |
pubmed-article:17764544 | pubmed:abstractText | p53 is commonly inactivated by mutations in the DNA-binding domain in a wide range of cancers. As mutant p53 often influences response to therapy, effective and rapid methods to scan for mutations in TP53 are likely to be of clinical value. We therefore evaluated the use of high resolution melting (HRM) as a rapid mutation scanning tool for TP53 in tumour samples. | lld:pubmed |
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pubmed-article:17764544 | pubmed:language | eng | lld:pubmed |
pubmed-article:17764544 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17764544 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:17764544 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17764544 | pubmed:issn | 1471-2407 | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:DerwinskiBB | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:DobrovicAlexa... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:BrentonJames... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:FoxStephen... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:Etemadmoghada... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:AhmedAhmed... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:BowtellDavid... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:HylandSarah... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:KrypuyMichael... | lld:pubmed |
pubmed-article:17764544 | pubmed:author | pubmed-author:Australian... | lld:pubmed |
pubmed-article:17764544 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:17764544 | pubmed:volume | 7 | lld:pubmed |
pubmed-article:17764544 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17764544 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17764544 | pubmed:pagination | 168 | lld:pubmed |
pubmed-article:17764544 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
pubmed-article:17764544 | pubmed:meshHeading | pubmed-meshheading:17764544... | lld:pubmed |
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pubmed-article:17764544 | pubmed:meshHeading | pubmed-meshheading:17764544... | lld:pubmed |
pubmed-article:17764544 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17764544 | pubmed:articleTitle | High resolution melting for mutation scanning of TP53 exons 5-8. | lld:pubmed |
pubmed-article:17764544 | pubmed:affiliation | Molecular Pathology Research and Development Laboratory, Department of Pathology, Peter MacCallum Cancer Centre, Locked Bag 1, A'Beckett St, Melbourne, Victoria 8006, Australia. michael.krypuy@petermac.org | lld:pubmed |
pubmed-article:17764544 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:17764544 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:17764544 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
pubmed-article:17764544 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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