Minimal residual disease diagnostics in acute lymphoblastic leukaemia: impact of primer characteristics and size of junctional regions
Author:
Affiliation:
1. Department of Immunology; Erasmus MC; University Medical Centre Rotterdam; Rotterdam The Netherlands
2. Department of Experimental immunohematology; Sanquin; Amsterdam The Netherlands
3. Dutch Childhood Oncology Group; The Hague The Netherlands
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjh.12621/fullpdf
Reference8 articles.
1. Minimal residual disease-directed risk stratification using real-time quantitative PCR analysis of immunoglobulin and T-cell receptor gene rearrangements in the international multicenter trial AIEOP-BFM ALL 2000 for childhood acute lymphoblastic leukemia;Flohr;Leukemia,2008
2. Risk-adapted therapy: lessons from childhood acute lymphoblastic leukemia;Schrappe;The Hematology Journal,2002
3. Why and how to quantify minimal residual disease in acute lymphoblastic leukemia?;Szczepanski;Leukemia,2007
4. MRD detection in acute lymphoblastic leukemia patients using Ig/TCR gene rearrangements as targets for real-time quantitative PCR;Velden;Methods in Molecular Biology,2009
5. T cell receptor gamma gene rearrangements as targets for detection of minimal residual disease in acute lymphoblastic leukemia by real-time quantitative PCR analysis;Velden;Leukemia,2002
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