- 関
- 細胞遺伝学的転座を伴う急性骨髄性白血病？。急性骨髄性白血病
WordNet
- a message whose ingenuity or verbal skill or incongruity has the power to evoke laughter (同)humor, humour, witticism, wittiness
- pertaining to or referring to origin; "genetic history reconstructs the origins of a literary work"
- of or relating to the science of genetics; "genetic research" (同)genetical
- the 1st letter of the Roman alphabet (同)a
- the blood group whose red cells carry the A antigen (同)type_A, group A
PrepTutorEJDIC
- 《随伴・協調》…『と』,と共に,といっしょに / 《所有・所持》…『を持っている』,がある,の付いた / 《道具・手段》…『で』,を使って / 《財料・供給物》…『で』,を与えて / …を支持して,に賛成して / …『に反対(敵対)して』,を相手として / …『と同時に』,と同様に / …『に比べて』,に比例して / 《様態》《名詞を伴い副詞句として》『…で』,を示して,をもって / 《付帯状競》…『して』,しながら / 《譲歩》…がありながら,にもかかわらず / 『…が原因で』,のために,…で / …に任せて,のもとにあずけて,のところに / …に関して,について / …から離れて / 《連結・混合》…と / 《副詞と共に命令文で》
- 知る(know)
- 〈U〉『機知』,機転,ウィット / 〈C〉『機知に富む人』,機転のきく人 / 《複数形で;単数扱い》『理解(表現)力』,知性 / 《複数形で》(物事を見抜いたりもくろんだりする)才覚,才知 / 《複数形で;単数扱い》正気
- answer / ampere
- 再発する;繰り返し起こる
UpToDate Contents
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English Journal
- Cytogenetic profiles of 2806 patients with acute myeloid leukemia-a retrospective multicenter nationwide study.
- Byun JM1, Kim YJ2, Yoon HJ3, Kim SY3, Kim HJ4, Yoon J4, Min YH5, Cheong JW5, Park J6, Lee JH6, Hong DS7, Park SK7, Kim HJ8, Ahn JS8, Shin HJ9, Chung JS9, Lee WS10, Lee SM10, Park Y11, Kim BS11, Lee JH12, Lee KH12, Jung CW13, Jang JH13, Min WS14, Park TS15; AML/MDS working party of Korean Society of Hematology.
- Annals of hematology.Ann Hematol.2016 May 26. [Epub ahead of print]
- The cytogenetic and molecular data is recognized as the most valuable prognostic factor in acute myeloid leukemia (AML). Our aim was to systemically analyze the cytogenetics of Korean AML patients and to compare the cytogenetic profiles of various races to identify possible geographic heterogeneity.
- PMID 27230620
- RUNX1 mutations in acute myeloid leukemia are associated with distinct clinico-pathologic and genetic features.
- Gaidzik VI1, Teleanu V1, Papaemmanuil E2, Weber D1, Paschka P1, Hahn J1, Wallrabenstein T1, Kolbinger B1, Köhne CH3, Horst HA4, Brossart P5, Held G6, Kündgen A7, Ringhoffer M8, Götze K9, Rummel M10, Gerstung M2, Campbell P2, Kraus JM11, Kestler HA11, Thol F12, Heuser M12, Schlegelberger B12, Ganser A12, Bullinger L1, Schlenk RF1, Döhner K1, Döhner H1.
- Leukemia.Leukemia.2016 May 3. doi: 10.1038/leu.2016.126. [Epub ahead of print]
- We evaluated the frequency, genetic architecture, clinico-pathologic features, and prognostic impact of RUNX1 mutations in 2439 adult patients with newly diagnosed acute myeloid leukemia (AML). RUNX1 mutations were found in 245 of 2439 (10%) patients; were almost mutually exclusive of AML with recur
- PMID 27137476
- Recurrent genetic abnormalities can be used for risk-group stratification in pediatric AMKL: results of a retrospective intergroup study.
- de Rooij JD1, Masetti R2, van den Heuvel-Eibrink MM3, Cayuela JM4, Trka J5, Reinhardt D6, Rasche M6, Sonneveld E7, Alonzo TA8, Fornerod M1, Zimmermann M9, Pigazzi M10, Pieters R3, Meshinchi S11, Zwaan CM12, Locatelli F13.
- Blood.Blood.2016 Apr 25. pii: blood-2016-01-695551. [Epub ahead of print]
- Genetic abnormalities and early treatment response are the main prognostic factors in acute myeloid leukemia (AML). Acute megakaryoblastic leukemia (AMKL) is a rare subtype of AML. Deep sequencing has identified CBFA2T3/GLIS2 and NUP98/KDM5A as recurrent aberrations, occurring in similar frequencies
- PMID 27114462
Japanese Journal
- 急性骨髄性白血病の病型分類と染色体異常-東京女子医科大学病院血液内科の過去28年間300症例における解析-
- 岡田 美智子,宇佐美 明美,岡嶋 香 [他],三浦 裕子,兒玉 聖子,志村 華絵,田中 紀奈,三橋 健次郎,石山 みどり,風間 啓至,吉永 健太郎,今井 陽一,志関 雅幸,森 直樹,寺村 正尚,泉二 登志子,OKADA Michiko,USAMI Akemi,OKAJIMA Kaori,MIURA Hiroko,KODAMA Shoko,SHIMURA Hanae,TANAKA Norina,MITSUHASHI Kenjiro,ISHIYAMA Midori,KAZAMA Hiroshi,YOSHINAGA Kentaro,IMAI Yoichi,SHISEKI Masayuki,MORI Naoki,TERAMURA Masanao,MOTOJI Toshiko
- 東京女子医科大学雑誌 83(E2), E539-E547, 2013-03-31
- … 28年間に亘り、染色体分析を行ってきた当科の急性骨髄性白血病(AML)300例の分析結果を報告する。 … 症例の内訳はWHO分類で特定の遺伝子異常を有するAMLとして、t(8;21)が25例、t(15;17)が36例、inv(16)が8例、t(9;11)が2例、t(6;9)が1例あった。 …
- NAID 110009575063
Related Links
- The American Society of Hematology (ASH) Image Bank is intended to serve as a comprehensive reference and teaching tool that is widely accessible to physicians and hematology students around the world.
- 1 Jan 2009 ... The four categories include AML with recurrent genetic abnormalities, AML with multilineage dysplasia, therapy-related AML and myelodysplastic syndromes, and AML not otherwise categorized, which roughly correlates with ...
★リンクテーブル★
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- 英
- AML with recurrent genetic abnormalities？
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- 急性骨髄性白血病。再現性のある染色体転座を伴うAML AMLs with recurrent cytogenetic translocations
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- 英
- AML with recurrent genetic abnormalities
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- 急性骨髄性白血病
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- iterative、recurrence、recurrently、regression、relapsing、repetitive
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- gene、genetically、heritable、heritably
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