| pubmed-article:12086872 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:12086872 | lifeskim:mentions | umls-concept:C0033325 | lld:lifeskim |
| pubmed-article:12086872 | lifeskim:mentions | umls-concept:C0023452 | lld:lifeskim |
| pubmed-article:12086872 | lifeskim:mentions | umls-concept:C0752248 | lld:lifeskim |
| pubmed-article:12086872 | lifeskim:mentions | umls-concept:C0008902 | lld:lifeskim |
| pubmed-article:12086872 | lifeskim:mentions | umls-concept:C0449560 | lld:lifeskim |
| pubmed-article:12086872 | lifeskim:mentions | umls-concept:C1880355 | lld:lifeskim |
| pubmed-article:12086872 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:12086872 | pubmed:dateCreated | 2002-6-27 | lld:pubmed |
| pubmed-article:12086872 | pubmed:abstractText | Treatment of pediatric acute lymphoblastic leukemia (ALL) is based on the concept of tailoring the intensity of therapy to a patient's risk of relapse. To determine whether gene expression profiling could enhance risk assignment, we used oligonucleotide microarrays to analyze the pattern of genes expressed in leukemic blasts from 360 pediatric ALL patients. Distinct expression profiles identified each of the prognostically important leukemia subtypes, including T-ALL, E2A-PBX1, BCR-ABL, TEL-AML1, MLL rearrangement, and hyperdiploid >50 chromosomes. In addition, another ALL subgroup was identified based on its unique expression profile. Examination of the genes comprising the expression signatures provided important insights into the biology of these leukemia subgroups. Further, within some genetic subgroups, expression profiles identified those patients that would eventually fail therapy. Thus, the single platform of expression profiling should enhance the accurate risk stratification of pediatric ALL patients. | lld:pubmed |
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| pubmed-article:12086872 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12086872 | pubmed:language | eng | lld:pubmed |
| pubmed-article:12086872 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:12086872 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:12086872 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:12086872 | pubmed:month | Mar | lld:pubmed |
| pubmed-article:12086872 | pubmed:issn | 1535-6108 | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:ZhouXiaodongX | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:XXX | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:PuiChing-HonC... | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:EvansWilliam... | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:RellingMary... | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:WongLimsoonL | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:RaimondiSusan... | lld:pubmed |
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| pubmed-article:12086872 | pubmed:author | pubmed-author:ShurtleffShei... | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:DowningJames... | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:LiJinyanJ | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:RossMary EME | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:YeohEng-JuhEJ | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:BehmFred GFG | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:WilliamsW... | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:PatelDivyenD | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:MahfouzRamiR | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:PatelAnamiA | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:WilkinsDawnD | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:LiuHuiqingH | lld:pubmed |
| pubmed-article:12086872 | pubmed:author | pubmed-author:NaeveClaytonC | lld:pubmed |
| pubmed-article:12086872 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:12086872 | pubmed:volume | 1 | lld:pubmed |
| pubmed-article:12086872 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:12086872 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:12086872 | pubmed:pagination | 133-43 | lld:pubmed |
| pubmed-article:12086872 | pubmed:dateRevised | 2007-11-15 | lld:pubmed |
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| pubmed-article:12086872 | pubmed:year | 2002 | lld:pubmed |
| pubmed-article:12086872 | pubmed:articleTitle | Classification, subtype discovery, and prediction of outcome in pediatric acute lymphoblastic leukemia by gene expression profiling. | lld:pubmed |
| pubmed-article:12086872 | pubmed:affiliation | Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. | lld:pubmed |
| pubmed-article:12086872 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:12086872 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:12086872 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:12086872 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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