Detection of minimal residual disease in peripheral blood stem cells from two acute myeloid leukemia patients with trisomy 8 predicts early relapse after autologous bone marrow transplantation-Reference-Cited by-同舟云学术

Detection of minimal residual disease in peripheral blood stem cells from two acute myeloid leukemia patients with trisomy 8 predicts early relapse after autologous bone marrow transplantation

Published:2002-02 Issue:1 Volume:133 Page:98-101
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Scaravaglio Patrizia,Guglielmelli Tommasina,Giugliano Emilia,Marmont Filippo,Audisio Ernesta,Gallo Eugenio,Saglio Giuseppe,Rege-Cambrin Giovanna

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

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4. Early Detection of Relapse by Prospective Reverse Transcriptase-Polymerase Chain Reaction Analysis of the PML/RARα Fusion Gene in Patients With Acute Promyelocytic Leukemia Enrolled in the GIMEMA-AIEOP Multicenter “AIDA” Trial

5. Pre-clinical evaluation of probes to detect t(8;21) AML minimal residual disease by fluorescence in situ hybridization;Paskulin;Genes Chromosomes Cancer,1998

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1. Risk Stratification, Measurable Residual Disease, and Outcomes of AML Patients with a Trisomy 8 Undergoing Allogeneic Hematopoietic Stem Cell Transplantation;Cancers;2021-11-13

2. Trisomy 8 in acute myeloid leukemia;Expert Review of Hematology;2019-09-26

3. Use of Fluorescence In Situ Hybridization to Detect Minimal Residual Disease in Hematopoietic Stem Cell Assays from Peripheral Blood Stem Cells of 2 Patients with Trisomy 8 Acute Myeloid Leukemia;Stem Cells and Development;2004-02

4. Trisomy 8 in Philadelphia-negative cells during imatinib therapy;American Journal of Hematology;2004

5. Determination of cutoff values to detect small aneuploid clones by interphase fluorescence in situ hybridization: the Poisson model is a more appropriate approach. Should single-cell trisomy 8 be considered a clonal defect?;Cancer Genetics and Cytogenetics;2003-12