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Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells
http://hdl.handle.net/2297/19612
http://hdl.handle.net/2297/19612b3758e2e-3223-43ec-a8a2-b02691e33c58
| 名前 / ファイル | ライセンス | アクション |
|---|---|---|
ME-PR-AKAGI-T-1301.pdf (217.8 kB)
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| Item type | 学術雑誌論文 / Journal Article(1) | |||||
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| 公開日 | 2017-10-03 | |||||
| タイトル | ||||||
| タイトル | Single nucleotide polymorphism genomic arrays analysis of t(8;21) acute myeloid leukemia cells | |||||
| 言語 | ||||||
| 言語 | eng | |||||
| 資源タイプ | ||||||
| 資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||
| 資源タイプ | journal article | |||||
| 著者 |
Akagi, Tadayuki
× Akagi, Tadayuki× Shih, Lee-Yung× Ogawa, Seishi× Gerss, Joachim× Moore, Stephen R.× Schreck, Rhona× Kawamata, Norihiko× Liang, Der-Cherng× Sanada, Masashi× Nannya, Yasuhito× Deneberg, Stefan× Zachariadis, Vasilios× Nordgren, Ann× Song, Jee Hoon× Dugas, Martin× Lehmann, Sören× Koeffler, H.Phillip |
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| 提供者所属 | ||||||
| 内容記述タイプ | Other | |||||
| 内容記述 | 金沢大学医薬保健研究域医学系 | |||||
| 書誌情報 |
Haematologica 巻 94, 号 9, p. 1301-1309, 発行日 2009-09-01 |
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| ISSN | ||||||
| 収録物識別子タイプ | ISSN | |||||
| 収録物識別子 | 0390-6078 | |||||
| NCID | ||||||
| 収録物識別子タイプ | NCID | |||||
| 収録物識別子 | AA00660912 | |||||
| DOI | ||||||
| 関連タイプ | isIdenticalTo | |||||
| 識別子タイプ | DOI | |||||
| 関連識別子 | 10.3324/haematol.2009.005744 | |||||
| 出版者 | ||||||
| 出版者 | FERRATA STORTI FOUNDATION | |||||
| 抄録 | ||||||
| 内容記述タイプ | Abstract | |||||
| 内容記述 | 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. ©2009 Ferrata Storti Foundation. | |||||
| 著者版フラグ | ||||||
| 出版タイプ | VoR | |||||
| 出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||
