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karyotype analysis

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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/09/06 15:37:21」(JST)

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  • Genome-wide analysis of cytogenetic aberrations in ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia.
  • Borst L, Wesolowska A, Joshi T, Borup R, Nielsen FC, Andersen MK, Jonsson OG, Wehner PS, Wesenberg F, Frost BM, Gupta R, Schmiegelow K.SourceClinic for Paediatric and Adolescent Medicine, The Juliane Marie Centre, The University Hospital Rigshospitalet, Copenhagen.
  • British journal of haematology.Br J Haematol.2012 May;157(4):476-82. doi: 10.1111/j.1365-2141.2012.09083.x. Epub 2012 Mar 7.
  • The chromosomal translocation t(12;21) resulting in the ETV6/RUNX1 fusion gene is the most frequent structural cytogenetic abnormality among patients with childhood acute lymphoblastic leukaemia (ALL). We investigated 62 ETV6/RUNX1-positive childhood ALL patients by single nucleotide polymorphism ar
  • PMID 22404039
  • The impact of the genetic background on the genome make-up of tumor cells.
  • Falck E, Behboudi A, Klinga-Levan K.SourceSystems Biology Research Centre-Tumor Biology, School of Life Sciences, University of Skövde, Skövde, Sweden.
  • Genes, chromosomes & cancer.Genes Chromosomes Cancer.2012 May;51(5):438-46. doi: 10.1002/gcc.21929. Epub 2012 Jan 17.
  • Endometrial adenocarcinoma (EAC) is the most common form of malignancy in the female genital tract, ranking as the fourth leading form of invasive tumors that affect women. The BDII inbred rat strain has been used as a powerful tumor model in studies of the genetic background of EAC. Females from th
  • PMID 22250046


  • 胎児染色体検査とマイクロアレイ検査(<特集>出生前遺伝学的検査)
  • 山田 崇弘
  • 日本産科婦人科學會雜誌 66(3), 982-988, 2014-03-01
  • NAID 110009810633
  • 染色体分析の今後 : マイクロアレイ染色体検査 (第32回東海・北陸支部例会 シンポジウム : 個別化医療の新展開にむけて : GWAS・CGH・NGSの活用)
  • 山本 俊至
  • 臨床病理 : 日本臨床検査医学会誌 62(1), 75-82, 2014-01
  • NAID 40019974945
  • 濾胞性リンパ腫に対するRFM療法後に発症した治療関連慢性骨髄性白血病
  • 柴崎 美緒,住 昌彦,武田 航 [他],桐原 健彦,栗原 太郎,佐藤 慶二郎,植木 俊充,廣島 由紀,上野 真由美,市川 直明,森 勇一,小林 光
  • 臨床血液 55(8), 970-974, 2014
  • 症例は61歳女性。52歳時に右乳癌に対し乳房温存術・放射線療法の既往あり。2007年に濾胞性リンパ腫を発症しRFM療法(リツキシマブ,フルダラビン,ミトキサントロン)で完全寛解となり経過観察中,2010年に慢性期慢性骨髄性白血病(CML-CP)を発症した。イマチニブで細胞遺伝学的完全寛解(CCyR)となったが,2013年1月に末梢血でリンパ芽球を65%認めリンパ芽球性急性転化と診断,染色体検査でフ …
  • NAID 130004688012


Karyotyping is a test to examine chromosomes in a sample of cells. This test can help identify genetic problems as the cause of a disorder or disease. How the Test is Performed The test can be performed on almost any tissue ...
Karyotyping also may be done to find out whether chromosomal problems may have caused a fetus to be stillborn. Find out the cause of a baby's birth defects or disability. Help determine the appropriate treatment for some types. ...


위의 사진은 Karyotyping이라는 ZooWeb - Karyotype, 46, XY downloadMetaClass Karyotyping + FISH System Figure 2. G-banding normal karyotyping of developments in the foetus. By karyotyping State that, in karyotyping

リンク元核型分析」「karyotype analysis
拡張検索spectral karyotyping法」「spectral karyotyping



karyotypingkaryotype analysiscaryotype analysis

karyotype analysis」




spectral karyotyping法」


spectral karyotyping method

spectral karyotyping」