Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome-Reference-Cited by-同舟云学术

Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

Published:2009-10-15 Issue:1 Volume:24 Page:242-246
ISSN:0887-6924
Container-title:Leukemia
language:en
Short-container-title:Leukemia

Author:

Jongmans M C J,Kuiper R P,Carmichael C L,Wilkins E J,Dors N,Carmagnac A,Schouten-van Meeteren A Y N,Li X,Stankovic M,Kamping E,Bengtsson H,Schoenmakers E F P M,van Kessel A Geurts,Hoogerbrugge P M,Hahn C N,Brons P P,Scott H S,Hoogerbrugge N

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Link

http://www.nature.com/articles/leu2009210.pdf

Reference8 articles.

1. Owen CJ, Toze CL, Koochin A, Forrest DL, Smith CA, Stevens JM et al. Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy. Blood 2008; 112: 4639–4645.

2. Song WJ, Sullivan MG, Legare RD, Hutchings S, Tan X, Kufrin D et al. Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia. Nat Genet 1999; 23: 166–175.

3. Michaud J, Simpson KM, Escher R, Buchet-Poyau K, Beissbarth T, Carmichael C et al. Integrative analysis of RUNX1 downstream pathways and target genes. BMC Genomics 2008; 31: 363.

4. Mikhail FM, Sinha KK, Saunthararajah Y, Nucifora G . Normal and transforming functions of RUNX1: a perspective. J Cell Physiol 2006; 207: 582–593.

5. Renneville A, Roumier C, Biggio V, Nibourel O, Boissel N, Fenaux P et al. Cooperating gene mutations in acute myeloid leukemia: a review of the literature. Leukemia 2008; 22: 915–931.

Cited by 83 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Updates on germline predisposition in pediatric hematologic malignancies: What is the role of flow cytometry?;Cytometry Part B: Clinical Cytometry;2024-06-28

2. Germline Variants and Characteristic Features of Hereditary Hematological Malignancy Syndrome;International Journal of Molecular Sciences;2024-01-04

3. Germline Predisposition in Hematologic Malignancies;Comprehensive Hematology and Stem Cell Research;2024

4. Diagnosing familial platelet disorder with predisposition to myeloid malignancy: Lessons learned from a germline whole‐gene deletion of RUNX1;International Journal of Laboratory Hematology;2023-11-12

5. Germline and somatic drivers in inherited hematologic malignancies;Frontiers in Oncology;2023-10-13