Literature DB >> 21764131

Multiplex ligation-dependent probe amplification for detection of chromosomal abnormalities in myelodysplastic syndrome and acute myeloid leukemia.

Amber C Donahue1, Adam K Abdool, Renu Gaur, Jay G Wohlgemuth, Chen-Hsiung Yeh.   

Abstract

Current strategies for detecting chromosome abnormalities in MDS/AML include FISH or traditional cytogenetics. MLPA detects abnormalities in multiple loci simultaneously, with higher resolution and throughput. Peripheral blood from 50 healthy subjects was used to establish probe-specific reference ranges, increasing MLPA sensitivity and specificity. MLPA was then performed on 110 FISH-tested blood or bone marrow samples from suspected leukemia patients. Our novel MLPA analysis system combined maximum stringency with sensitive detection of low-frequency abnormalities. Accuracy/specificity of MLPA were excellent compared to FISH. Our MLPA analysis/interpretation method provides a clinically robust, high-throughput, high-resolution option for detection of abnormalities associated with MDS/AML.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21764131     DOI: 10.1016/j.leukres.2011.06.019

Source DB:  PubMed          Journal:  Leuk Res        ISSN: 0145-2126            Impact factor:   3.156


  5 in total

1.  Multiplex ligation-dependent probe amplification and fluorescence in situ hybridization for detecting chromosome abnormalities in myelodysplastic syndromes: A retrospective study.

Authors:  Xiaofei Ai; Bing Li; Zefeng Xu; Jinqin Liu; Tiejun Qin; Qinghua Li; Zhijian Xiao
Journal:  Medicine (Baltimore)       Date:  2021-05-07       Impact factor: 1.889

Review 2.  Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.

Authors:  Liborio Stuppia; Ivana Antonucci; Giandomenico Palka; Valentina Gatta
Journal:  Int J Mol Sci       Date:  2012-03-08       Impact factor: 6.208

3.  Multiplex ligation-dependent probe amplification assay identifies additional copy number changes compared with R-band karyotype and provide more accuracy prognostic information in myelodysplastic syndromes.

Authors:  Jingya Wang; Xiaofei Ai; Tiejun Qin; Zefeng Xu; Yue Zhang; Jinqin Liu; Bing Li; Liwei Fang; Hongli Zhang; Lijuan Pan; Naibo Hu; Shiqiang Qu; Wenyu Cai; Kun Ru; Yujiao Jia; Gang Huang; Zhijian Xiao
Journal:  Oncotarget       Date:  2017-01-03

4.  Multiplex ligation-dependent probe amplification identifies copy number changes in normal and undetectable karyotype MDS patients.

Authors:  Jing Ma; Xiaofei Ai; Jinhuan Wang; Limin Xing; Chen Tian; Hongliang Yang; Yong Yu; Haifeng Zhao; Xiaofang Wang; Zhigang Zhao; Yafei Wang; Zeng Cao
Journal:  Ann Hematol       Date:  2021-05-15       Impact factor: 3.673

5.  A molecular diagnostic approach able to detect the recurrent genetic prognostic factors typical of presenting myeloma.

Authors:  Eileen M Boyle; Paula Z Proszek; Martin F Kaiser; Dil Begum; Nasrin Dahir; Suvi Savola; Christopher P Wardell; Xavier Leleu; Fiona M Ross; Laura Chiecchio; Gordon Cook; Mark T Drayson; Richard G Owen; John M Ashcroft; Graham H Jackson; James Anthony Child; Faith E Davies; Brian A Walker; Gareth J Morgan
Journal:  Genes Chromosomes Cancer       Date:  2014-10-07       Impact factor: 5.006

  5 in total

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