Matches in SemOpenAlex for { <https://semopenalex.org/work/W2416232867> ?p ?o ?g. }
Showing items 1 to 78 of
78
with 100 items per page.
- W2416232867 endingPage "S61" @default.
- W2416232867 startingPage "S55" @default.
- W2416232867 abstract "Microarrays are at the center of a revolution in biotechnology, allowing researchers to screen tens of thousands of genes simultaneously. Typically, they have been used in exploratory research to help formulate hypotheses. In most cases, this phase is followed by a more focused, hypothesis-driven stage in which certain specific biological processes and pathways are thought to be involved. Since a single biological process can still involve hundreds of genes, microarrays are still the preferred approach as proven by the availability of focused arrays from several manufacturers. Because focused arrays from different manufacturers use different sets of genes, each array will represent any given regulatory pathway to a different extent. We argue that a functional analysis of the arrays available should be the most important criterion used in the array selection. We developed Onto-Compare as a database that can provide this functionality, based on the Gene Ontology Consortium nomenclature. We used this tool to compare several arrays focused on apoptosis, oncogenes, and tumor suppressors. We considered arrays from BD Biosciences Clontech, PerkinElmer, Sigma-Genosys, and SuperArray. We showed that among the oncogene arrays, the PerkinElmer MICROMAX™ oncogene microarray has a better representation of oncogenesis, protein phosphorylation, and negative control of cell proliferation. The comparison of the apoptosis arrays showed that most apoptosis-related biological processes are equally well represented on the arrays considered. However, functional categories such as immune response, cell-cell signaling, cell-surface receptor linked signal transduction, and interleukins are better represented on the Sigma-Genosys Panorama™ human apoptosis array. At the same time, processes such as cell cycle control, oncogenesis, and negative control of cell proliferation are better represented on the BD Biosciences Clontech Atlas Select™ human apoptosis array." @default.
- W2416232867 created "2016-06-24" @default.
- W2416232867 creator A5006190733 @default.
- W2416232867 creator A5007987600 @default.
- W2416232867 creator A5043849903 @default.
- W2416232867 creator A5083763463 @default.
- W2416232867 date "2003-03-01" @default.
- W2416232867 modified "2023-10-12" @default.
- W2416232867 title "Assessing the Functional Bias of Commercial Microarrays Using the Onto-Compare Database" @default.
- W2416232867 cites W1535641839 @default.
- W2416232867 cites W1597538863 @default.
- W2416232867 cites W1964627042 @default.
- W2416232867 cites W1986891966 @default.
- W2416232867 cites W1993803613 @default.
- W2416232867 cites W1998902445 @default.
- W2416232867 cites W2012951653 @default.
- W2416232867 cites W2021729172 @default.
- W2416232867 cites W2037500862 @default.
- W2416232867 cites W2064208261 @default.
- W2416232867 cites W2073005600 @default.
- W2416232867 cites W2097413644 @default.
- W2416232867 cites W2103017472 @default.
- W2416232867 cites W2120262606 @default.
- W2416232867 cites W2122128696 @default.
- W2416232867 cites W2135187880 @default.
- W2416232867 cites W2137476312 @default.
- W2416232867 cites W3015571647 @default.
- W2416232867 doi "https://doi.org/10.2144/mar03draghici" @default.
- W2416232867 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12664686" @default.
- W2416232867 hasPublicationYear "2003" @default.
- W2416232867 type Work @default.
- W2416232867 sameAs 2416232867 @default.
- W2416232867 citedByCount "13" @default.
- W2416232867 crossrefType "journal-article" @default.
- W2416232867 hasAuthorship W2416232867A5006190733 @default.
- W2416232867 hasAuthorship W2416232867A5007987600 @default.
- W2416232867 hasAuthorship W2416232867A5043849903 @default.
- W2416232867 hasAuthorship W2416232867A5083763463 @default.
- W2416232867 hasBestOaLocation W24162328671 @default.
- W2416232867 hasConcept C104317684 @default.
- W2416232867 hasConcept C150194340 @default.
- W2416232867 hasConcept C186836561 @default.
- W2416232867 hasConcept C54355233 @default.
- W2416232867 hasConcept C60644358 @default.
- W2416232867 hasConcept C70721500 @default.
- W2416232867 hasConcept C86803240 @default.
- W2416232867 hasConcept C95371953 @default.
- W2416232867 hasConceptScore W2416232867C104317684 @default.
- W2416232867 hasConceptScore W2416232867C150194340 @default.
- W2416232867 hasConceptScore W2416232867C186836561 @default.
- W2416232867 hasConceptScore W2416232867C54355233 @default.
- W2416232867 hasConceptScore W2416232867C60644358 @default.
- W2416232867 hasConceptScore W2416232867C70721500 @default.
- W2416232867 hasConceptScore W2416232867C86803240 @default.
- W2416232867 hasConceptScore W2416232867C95371953 @default.
- W2416232867 hasIssue "3S" @default.
- W2416232867 hasLocation W24162328671 @default.
- W2416232867 hasLocation W24162328672 @default.
- W2416232867 hasLocation W24162328673 @default.
- W2416232867 hasOpenAccess W2416232867 @default.
- W2416232867 hasPrimaryLocation W24162328671 @default.
- W2416232867 hasRelatedWork W1971437990 @default.
- W2416232867 hasRelatedWork W2006024165 @default.
- W2416232867 hasRelatedWork W2016348706 @default.
- W2416232867 hasRelatedWork W2362947020 @default.
- W2416232867 hasRelatedWork W2363311673 @default.
- W2416232867 hasRelatedWork W2381315635 @default.
- W2416232867 hasRelatedWork W3032874291 @default.
- W2416232867 hasRelatedWork W3141198878 @default.
- W2416232867 hasRelatedWork W74695042 @default.
- W2416232867 hasRelatedWork W18532184 @default.
- W2416232867 hasVolume "34" @default.
- W2416232867 isParatext "false" @default.
- W2416232867 isRetracted "false" @default.
- W2416232867 magId "2416232867" @default.
- W2416232867 workType "article" @default.