| pubmed-article:19734423 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19734423 | lifeskim:mentions | umls-concept:C0007634 | lld:lifeskim |
| pubmed-article:19734423 | lifeskim:mentions | umls-concept:C1292774 | lld:lifeskim |
| pubmed-article:19734423 | lifeskim:mentions | umls-concept:C0017428 | lld:lifeskim |
| pubmed-article:19734423 | lifeskim:mentions | umls-concept:C0752046 | lld:lifeskim |
| pubmed-article:19734423 | lifeskim:mentions | umls-concept:C0936012 | lld:lifeskim |
| pubmed-article:19734423 | lifeskim:mentions | umls-concept:C1510941 | lld:lifeskim |
| pubmed-article:19734423 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:19734423 | pubmed:dateCreated | 2009-9-7 | lld:pubmed |
| pubmed-article:19734423 | pubmed:abstractText | Translocation of chromosomes 8 and 21, t(8;21), resulting in the AML1-ETO fusion gene, is associated with acute myeloid leukemia. We searched for additional genomic abnormalities in this acute myeloid leukemia subtype by performing single nucleotide polymorphism genomic arrays (SNP-chip) analysis on 48 newly diagnosed cases. Thirty-two patients (67%) had a normal genome by SNP-chip analysis (Group A), and 16 patients (33%) had one or more genomic abnormalities including copy number changes or copy number neutral loss of heterozygosity (Group B). Two samples had copy number neutral loss of heterozygosity on chromosome 6p including the PIM1 gene; and one of these cases had E135K mutation of Pim1. Interestingly, 38% of Group B and only 13% of Group A samples had a KIT-D816 mutation, suggesting that genomic alterations are often associated with a KIT-D816 mutation. Importantly, prognostic analysis revealed that overall survival and event-free survival of individuals in Group B were significantly worse than those in Group A. | lld:pubmed |
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| pubmed-article:19734423 | pubmed:language | eng | lld:pubmed |
| pubmed-article:19734423 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19734423 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19734423 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19734423 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:19734423 | pubmed:issn | 1592-8721 | lld:pubmed |
| pubmed-article:19734423 | pubmed:author | pubmed-author:AkagiTadayuki... | lld:pubmed |
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| pubmed-article:19734423 | pubmed:author | pubmed-author:OgawaSeishiS | lld:pubmed |
| pubmed-article:19734423 | pubmed:author | pubmed-author:NannyaYasuhit... | lld:pubmed |
| pubmed-article:19734423 | pubmed:author | pubmed-author:KawamataNorih... | lld:pubmed |
| pubmed-article:19734423 | pubmed:author | pubmed-author:ShihLee-YungL... | lld:pubmed |
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| pubmed-article:19734423 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19734423 | pubmed:volume | 94 | lld:pubmed |
| pubmed-article:19734423 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19734423 | pubmed:authorsComplete | Y | lld:pubmed |
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| pubmed-article:19734423 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19734423 | pubmed:articleTitle | Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells. | lld:pubmed |
| pubmed-article:19734423 | pubmed:affiliation | Department of Stem Cell Biology, Graduate School of Medical Science, Kanazawa University, 13-1 Takara-machi, Kanazawa, Ishikawa, Japan. tadayuki@staff.kanazawa-u.ac.jp | lld:pubmed |
| pubmed-article:19734423 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19734423 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:19734423 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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