pubmed-article:16768788 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C0025663 | lld:lifeskim |
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pubmed-article:16768788 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C0600596 | lld:lifeskim |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C1301627 | lld:lifeskim |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C1523987 | lld:lifeskim |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C1517945 | lld:lifeskim |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C2911684 | lld:lifeskim |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C2347858 | lld:lifeskim |
pubmed-article:16768788 | lifeskim:mentions | umls-concept:C0185117 | lld:lifeskim |
pubmed-article:16768788 | pubmed:dateCreated | 2006-8-3 | lld:pubmed |
pubmed-article:16768788 | pubmed:abstractText | Recent developments in DNA microarray technology led to a variety of open and closed devices and systems including high and low density microarrays for high-throughput screening applications as well as microarrays of lower density for specific diagnostic purposes. Beside predefined microarrays for specific applications manufacturers offer the production of custom-designed microarrays adapted to customers' wishes. Array based assays demand complex procedures including several steps for sample preparation (RNA extraction, amplification and sample labelling), hybridization and detection, thus leading to a high variability between several approaches and resulting in the necessity of extensive standardization and normalization procedures. | lld:pubmed |
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pubmed-article:16768788 | pubmed:language | eng | lld:pubmed |
pubmed-article:16768788 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:16768788 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:16768788 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:16768788 | pubmed:issn | 1471-2164 | lld:pubmed |
pubmed-article:16768788 | pubmed:author | pubmed-author:WiederandersB... | lld:pubmed |
pubmed-article:16768788 | pubmed:author | pubmed-author:EhrichtRR | lld:pubmed |
pubmed-article:16768788 | pubmed:author | pubmed-author:SlickersPP | lld:pubmed |
pubmed-article:16768788 | pubmed:author | pubmed-author:WenzIngridI | lld:pubmed |
pubmed-article:16768788 | pubmed:author | pubmed-author:SchülerSusann... | lld:pubmed |
pubmed-article:16768788 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:16768788 | pubmed:volume | 7 | lld:pubmed |
pubmed-article:16768788 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:16768788 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:16768788 | pubmed:pagination | 144 | lld:pubmed |
pubmed-article:16768788 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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pubmed-article:16768788 | pubmed:year | 2006 | lld:pubmed |
pubmed-article:16768788 | pubmed:articleTitle | An alternative method to amplify RNA without loss of signal conservation for expression analysis with a proteinase DNA microarray in the ArrayTube format. | lld:pubmed |
pubmed-article:16768788 | pubmed:affiliation | Institute of Biochemistry, Klinikum, Friedrich-Schiller-Universität Jena, Germany. susch@mti.uni-jena.de | lld:pubmed |
pubmed-article:16768788 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:16768788 | pubmed:publicationType | Comparative Study | lld:pubmed |
pubmed-article:16768788 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:16768788 | pubmed:publicationType | Validation Studies | lld:pubmed |