标题
RUNX1translocations and fusion genes in malignant hemopathies
作者
关键词
-
出版物
Future Oncology
Volume 7, Issue 1, Pages 77-91
出版商
Future Medicine Ltd
发表日期
2010-12-22
DOI
10.2217/fon.10.158
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Distinct clonal anomalies involving RUNX1 in acute myeloid leukemia at diagnosis and after bone marrow transplantation
- (2010) Etienne De Braekeleer et al. ANNALS OF HEMATOLOGY
- Cytogenetics in pre-B and B-cell acute lymphoblastic leukemia: a study of 208 patients diagnosed between 1981 and 2008
- (2010) Etienne De Braekeleer et al. CANCER GENETICS AND CYTOGENETICS
- Poor outcome in a pediatric patient with acute myeloid leukemia associated with a variant t(8;21) and trisomy 6
- (2009) Michael J. Kelly et al. CANCER GENETICS AND CYTOGENETICS
- A novel four-way t(6;16;21;8)(p21.3;p11.2;q22;q22) in acute myeloid leukemia with RUNX1/RUNX1T1 rearrangement
- (2009) Kyoung-Jin Park et al. CANCER GENETICS AND CYTOGENETICS
- Acute myeloid leukemia (M2) with a cryptic RUNX1/RUNX1T1 t(1;21;8)(p36;q22;q22) variant
- (2009) Carlos A. Tirado et al. CANCER GENETICS AND CYTOGENETICS
- Acute myeloid leukemia with t(16;21)(q24;q22) and eosinophilia: case report and review of the literature
- (2009) Il Joong Park et al. CANCER GENETICS AND CYTOGENETICS
- LPXN, a member of the paxillin superfamily, is fused toRUNX1in an acute myeloid leukemia patient with a t(11;21)(q12;q22) translocation
- (2009) Hai-Ping Dai et al. GENES CHROMOSOMES & CANCER
- Three way translocation in a new variant of t(8;21) acute myeloid leukemia involving Xp22
- (2009) BR Vundinti et al. INDIAN JOURNAL OF CANCER
- RUNX1 DNA-binding mutations and RUNX1-PRDM16 cryptic fusions in BCR-ABL+ leukemias are frequently associated with secondary trisomy 21 and may contribute to clonal evolution and imatinib resistance
- (2008) C. Roche-Lestienne et al. BLOOD
- Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1genes
- (2008) Véronique Gelsi-Boyer et al. BMC CANCER
- Molecular cytogenetic findings in a three-way novel variant of t(1;8;21)(p35;q22;q22): a unique relocation of the AML1/ETO fusion gene 1p35 in AML-M2
- (2008) Firoz Ahmad et al. CANCER GENETICS AND CYTOGENETICS
- RUNX1 rearrangements in acute myeloblastic leukemia relapsing after hematopoietic stem cell transplantation
- (2008) Nathalie Nadal et al. CANCER GENETICS AND CYTOGENETICS
- Complex t(8;19;21)(q22;p13;q22) as a sole abnormality in a patient with de novo acute myeloid leukemia
- (2008) Tae Sung Park et al. CANCER GENETICS AND CYTOGENETICS
- RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature
- (2008) Étienne De Braekeleer et al. CANCER GENETICS AND CYTOGENETICS
- Zfp64 participates in Notch signaling and regulates differentiation in mesenchymal cells
- (2008) K. Sakamoto et al. JOURNAL OF CELL SCIENCE
- Laboratory study of a complex translocation t(2;8;21) (p12;q22;q22) in a patient with acute myelogenous leukemia
- (2008) Hui Shao et al. LEUKEMIA & LYMPHOMA
- Complex t(8;13;21)(q22;q14;q22)–A Novel Variant of t(8;21) in a Patient with Acute Myeloid Leukemia (AML–M2)
- (2007) Achandira Muthappa Udayakumar et al. ARCHIVES OF MEDICAL RESEARCH
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started