نتایج جستجو برای: evi1

تعداد نتایج: 316  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2013
Vitalyi Senyuk Yunyuan Zhang Yang Liu Ming Ming Kavitha Premanand Lan Zhou Ping Chen Jianjun Chen Janet D Rowley Giuseppina Nucifora Zhijian Qian

MicroRNA-9 (miR-9) is emerging as a critical regulator of organ development and neurogenesis. It is also deregulated in several types of solid tumors; however, its role in hematopoiesis and leukemogenesis is not yet known. Here we show that miR-9 is detected in hematopoietic stem cells and hematopoietic progenitor cells, and that its expression increases during hematopoietic differentiation. Ec...

2006
Jan S. Sunde Howard Donninger Kongming Wu Michael E. Johnson Richard G. Pestell G. Scott Rose Samuel C. Mok John Brady Tomas Bonome Michael J. Birrer

Ovarian cancer is resistant to the antiproliferative effects of transforming growth factor-B (TGF-B); however, the mechanism of this resistance remains unclear. We used oligonucleotide arrays to profile 37 undissected, 68 microdissected advanced-stage, and 14 microdissected early-stage papillary serous cancers to identify signaling pathways involved in ovarian cancer. A total of seven genes inv...

Journal: :Blood 1996
S D Raynaud M Baens J Grosgeorge K Rodgers C D Reid M Dainton M Dyer J G Fuzibet N Gratecos B Taillan N Ayraud P Marynen

We have identified a new recurrent reciprocal translocation between chromosome 3 and 12 with breakpoints at bands 3q26 and 12p13, t(3;12)(q26;p13) in the malignant cells from five patients with acute transformation of myelodysplastic syndrome or blast crisis of chronic myelogenous leukemia. t(3;12)(q26;p13) appears as a rare but nonrandom event present in various myeloid leukemia subtypes, whic...

2013
Jaap Brand Martin H van Vliet Leonie de Best Peter JM Valk Henk E Viëtor Bob Löwenberg Erik H van Beers

High levels of BAALC, ERG, EVI1 and MN1 expression have been associated with shorter overall survival in AML but standardized and clinically validated assays are lacking. We have therefore developed and optimized an assay for standardized detection of these prognostic genes for patients with intermediate cytogenetic risk AML. In a training set of 147 intermediate cytogenetic risk cases we perfo...

Journal: :Blood 2005
Boris Calmels Cole Ferguson Mikko O Laukkanen Rima Adler Marion Faulhaber Hyeoung-Joon Kim Stephanie Sellers Peiman Hematti Manfred Schmidt Christof von Kalle Keiko Akagi Robert E Donahue Cynthia E Dunbar

Recent reports linking insertional activation of LMO2 following gene therapy for X-linked severe combined immunodeficiency (X-SCID) have led to a re-evaluation of risks following gene therapy with retroviral vectors. In our analysis of 702 integration sites in rhesus macaques that underwent transplantation up to 7 years earlier with autologous CD34+ cells transduced with amphotropic murine leuk...

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2017

Journal: :Blood 2005
Yang Du Nancy A Jenkins Neal G Copeland

Retroviruses can induce hematopoietic disease via insertional mutagenesis of cancer genes and provide valuable molecular tags for cancer gene discovery. Here we show that insertional mutagenesis can also identify genes that promote the immortalization of hematopoietic cells, which normally have only limited self-renewal. Transduction of mouse bone marrow cells with replication-incompetent murin...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
G M Cuenco G Nucifora R Ren

The human t(3;21)(q26;q22) translocation is found as a secondary mutation in some cases of chronic myelogenous leukemia during the blast phase and in therapy-related myelodysplasia and acute myelogenous leukemia. One result of this translocation is a fusion between the AML1, MDS1, and EVI1 genes, which encodes a transcription factor of approximately 200 kDa. The role of the AML1/MDS1/EVI1 (AME)...

Journal: :Blood 2008
Naoko Watanabe-Okochi Jiro Kitaura Ryoichi Ono Hironori Harada Yuka Harada Yukiko Komeno Hideaki Nakajima Tetsuya Nosaka Toshiya Inaba Toshio Kitamura

Myelodysplastic syndrome (MDS) is a hematopoietic stem-cell disorder characterized by trilineage dysplasia and susceptibility to acute myelogenous leukemia (AML). Analysis of molecular basis of MDS has been hampered by the heterogeneity of the disease. Recently, mutations of the transcription factor AML1/RUNX1 have been identified in 15% to 40% of MDS-refractory anemia with excess of blasts (RA...

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