Trisomy 13: prevalence and clinicopathologic correlates of another potentially lenalidomide-sensitive cytogenetic abnormality-Reference-Cited by-同舟云学术

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Trisomy 13: prevalence and clinicopathologic correlates of another potentially lenalidomide-sensitive cytogenetic abnormality

Published:2009-01-29 Issue:5 Volume:113 Page:1200-1201
ISSN:0006-4971
Container-title:Blood
language:en
Short-container-title:

Author:

Mesa Ruben A.,Hanson Curtis A.,Ketterling Rhett P.,Schwager Susan,Knudson Ryan A.,Tefferi Ayalew

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Link

http://ashpublications.org/blood/article-pdf/113/5/1200/1309401/zh800509001200.pdf

Reference4 articles.

1. Efficacy of lenalidomide in myelodysplastic syndromes.;List;N Engl J Med,2005

2. Lenalidomide therapy in myelofibrosis with myeloid metaplasia.;Tefferi;Blood,2006

3. Hematologic and cytogenetic response to lenalidomide monotherapy in acute myeloid leukemia arising from JAK2(V617F) positive, del(5)(q13q33) myelodysplastic syndrome.;Mesa;Leukemia,2006

4. Single-agent lenalidomide induces complete remission of acute myeloid leukemia in patients with isolated trisomy 13.;Fehniger;Blood,2009

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1. Cytogenetics in the management of myelodysplastic neoplasms (myelodysplastic syndromes, MDS): Guidelines from the groupe francophone de cytogénétique hématologique (GFCH);Current Research in Translational Medicine;2023-10

2. A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia;Cancer Genetics;2022-08

3. From cellular morphology to molecular and epigenetic anomalies of myelodysplastic syndromes;Genes, Chromosomes and Cancer;2018-11-18

4. Number of RUNX1 mutations, wild-type allele loss and additional mutations impact on prognosis in adult RUNX1-mutated AML;Leukemia;2017-07-28

5. Incidence and prognostic significance of isolated trisomies in adult acute myeloid leukemia: A population-based study from the Swedish AML registry;European Journal of Haematology;2017-03-09

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