pubmed-article:14671650 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0684224 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C1704387 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C1522642 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0021027 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0441472 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C1511790 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0032520 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0524889 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0678936 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0442711 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0038136 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C1707689 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C1571873 | lld:lifeskim |
pubmed-article:14671650 | lifeskim:mentions | umls-concept:C0206415 | lld:lifeskim |
pubmed-article:14671650 | pubmed:issue | 12 | lld:pubmed |
pubmed-article:14671650 | pubmed:dateCreated | 2003-12-12 | lld:pubmed |
pubmed-article:14671650 | pubmed:abstractText | In a European BIOMED-2 collaborative study, multiplex PCR assays have successfully been developed and standardized for the detection of clonally rearranged immunoglobulin (Ig) and T-cell receptor (TCR) genes and the chromosome aberrations t(11;14) and t(14;18). This has resulted in 107 different primers in only 18 multiplex PCR tubes: three VH-JH, two DH-JH, two Ig kappa (IGK), one Ig lambda (IGL), three TCR beta (TCRB), two TCR gamma (TCRG), one TCR delta (TCRD), three BCL1-Ig heavy chain (IGH), and one BCL2-IGH. The PCR products of Ig/TCR genes can be analyzed for clonality assessment by heteroduplex analysis or GeneScanning. The detection rate of clonal rearrangements using the BIOMED-2 primer sets is unprecedentedly high. This is mainly based on the complementarity of the various BIOMED-2 tubes. In particular, combined application of IGH (VH-JH and DH-JH) and IGK tubes can detect virtually all clonal B-cell proliferations, even in B-cell malignancies with high levels of somatic mutations. The contribution of IGL gene rearrangements seems limited. Combined usage of the TCRB and TCRG tubes detects virtually all clonal T-cell populations, whereas the TCRD tube has added value in case of TCRgammadelta(+) T-cell proliferations. The BIOMED-2 multiplex tubes can now be used for diagnostic clonality studies as well as for the identification of PCR targets suitable for the detection of minimal residual disease. | lld:pubmed |
pubmed-article:14671650 | pubmed:language | eng | lld:pubmed |
pubmed-article:14671650 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14671650 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:14671650 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14671650 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14671650 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:14671650 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:14671650 | pubmed:month | Dec | lld:pubmed |
pubmed-article:14671650 | pubmed:issn | 0887-6924 | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:SmithJ LJL | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:GonzálezDD | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:GonzálezMM | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:HummelMM | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:MorganG JGJ | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:DroeseJJ | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:WhiteH EHE | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:LangerakA WAW | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:ParreiraAA | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:SchuuringEE | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:BastardCC | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:MacintyreE... | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:SpaargarenMM | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:LavenderF LFL | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:KnebaMM | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:BrüggemannMM | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:DaviFF | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:DelabesseEE | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:García-SanzRR | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:van DongenJ... | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:van... | lld:pubmed |
pubmed-article:14671650 | pubmed:author | pubmed-author:EvansP A SPA | lld:pubmed |
pubmed-article:14671650 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:14671650 | pubmed:volume | 17 | lld:pubmed |
pubmed-article:14671650 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:14671650 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:14671650 | pubmed:pagination | 2257-317 | lld:pubmed |
pubmed-article:14671650 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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pubmed-article:14671650 | pubmed:year | 2003 | lld:pubmed |
pubmed-article:14671650 | pubmed:articleTitle | Design and standardization of PCR primers and protocols for detection of clonal immunoglobulin and T-cell receptor gene recombinations in suspect lymphoproliferations: report of the BIOMED-2 Concerted Action BMH4-CT98-3936. | lld:pubmed |
pubmed-article:14671650 | pubmed:affiliation | Department of Immunology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands. j.j.m.vandongen@erasmusmc.nl | lld:pubmed |
pubmed-article:14671650 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:14671650 | pubmed:publicationType | Review | lld:pubmed |
pubmed-article:14671650 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
pubmed-article:14671650 | pubmed:publicationType | Multicenter Study | lld:pubmed |
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