High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression (Q63248736)

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English	High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression	article

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scholarly article

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31 January 2020

High-density single nucleotide polymorphism array analysis and ASXL1 gene mutation screening in chronic myeloid leukemia during disease progression (English)

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31 January 2020

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myeloid leukemia

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chronic myeloid leukemia

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Jacqueline Boultwood

1

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31 January 2020

Andrea Pellagatti

7

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31 January 2020

author name string

J Perry

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R Zaman

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31 January 2020

C Fernandez-Santamaria

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T Littlewood

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R Kusec

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31 January 2020

L Wang

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R E Clark

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31 January 2020

J S Wainscoat

10

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publication date

22 April 2010

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31 January 2020

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24

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6

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31 January 2020

1139-1145

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31 January 2020

https://scigraph.springernature.com/pub.10.1038/leu.2010.65

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Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining

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Chronic myelogenous leukemia: mechanisms underlying disease progression.

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Serial monitoring of BCR-ABL by peripheral blood real-time polymerase chain reaction predicts the marrow cytogenetic response to imatinib mesylate in chronic myeloid leukaemia

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Monitoring CML patients responding to treatment with tyrosine kinase inhibitors: review and recommendations for harmonizing current methodology for detecting BCR-ABL transcripts and kinase domain mutations and for expressing results

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Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays

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Mutations of ASXL1 gene in myeloproliferative neoplasms.

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Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.

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Extended tracts of homozygosity in outbred human populations

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MASL1, a candidate oncogene found in amplification at 8p23.1, is translocated in immunoblastic B-cell lymphoma cell line OCI-LY8.

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