Monitoring minimal residual disease by quantification of genomic chromosomal breakpoint sequences in acute leukemias with MLL aberrations-Reference-Cited by-同舟云学术

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Monitoring minimal residual disease by quantification of genomic chromosomal breakpoint sequences in acute leukemias with MLL aberrations

Published:2006-01-19 Issue:3 Volume:20 Page:451-457
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Burmeister T,Marschalek R,Schneider B,Meyer C,Gökbuget N,Schwartz S,Hoelzer D,Thiel E

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/2404082.pdf

Reference24 articles.

1. Pui CH, Relling MV, Downing JR . Acute lymphoblastic leukemia. N Engl J Med 2004; 350 (15): 1535–1548.

2. Schoch C, Schnittger S, Klaus M, Kern W, Hiddemann W, Haferlach T . AML with 11q23/MLL abnormalities as defined by the WHO classification: incidence, partner chromosomes, FAB subtype, age distribution, and prognostic impact in an unselected series of 1897 cytogenetically analyzed AML cases. Blood 2003; 102 (7): 2395–2402.

3. Gilliland DG, Jordan CT, Felix CA . The molecular basis of leukemia. Hematology (Am Soc Hematol Educ Program) 2004, 80–97.

4. Meyer C, Schneider B, Jakob S, Strehl S, Attarbaschi A, Schnittger S et al. The MLL recombinome of acute leukemias. 2005, submitted.

5. Pui CH, Chessells JM, Camitta B, Baruchel A, Biondi A, Boyett JM et al. Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements. Leukemia 2003; 17 (4): 700–706.

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4. Genomic breakpoint specific monitoring of measurable residual disease in pediatric non-standard risk acute myeloid leukemia;Haematologica;2023-06-22

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