نتایج جستجو برای: aml1

تعداد نتایج: 978  

Journal: :Blood 2003
Marianne Konrad Markus Metzler Simon Panzer Iris Ostreicher Martina Peham Reinald Repp Oskar A Haas Helmut Gadner E Renate Panzer-Grumayer

TEL/AML1-positive childhood acute lymphoblastic leukemias (ALLs) generally have low-risk features, but still about 20% of patients relapse. Our initial molecular genetic analyses in 2 off-treatment relapses suggested that the initial and relapse clones represent different subclones that evolved from a common TEL/AML1-positive, treatment-resistant precursor. In order to further elaborate on this...

2002
Tarja Niini

...................................................................................................... 9 INTRODUCTION ........................................................................................... 11 REVIEW OF THE LITERATURE.................................................................. 12 1. Normal development of blood cells ........................................................

Journal: :Blood 1990
J Oval O W Jones M Montoya R Taetle

A strictly factor-dependent cell line (UCSD/AML1) was established from a patient with the syndrome of multilineage acute leukemia with high platelets. The patient's cells and the cell line karyotype were 45,XX,-7,t(3;3)(q21;q26), typical of the syndrome of acute leukemia with high platelets. The cell line expresses CD34, CD7, TdT, and myeloid (CD13, CD14, CD33) and megakaryocyte/platelet (CD36,...

2016
Eva Gentner Naidu M. Vegi Medhanie A. Mulaw Tamoghna Mandal Shiva Bamezai Rainer Claus Alpaslan Tasdogan Leticia Quintanilla-Martinez Alexander Grunenberg Konstanze Döhner Hartmut Döhner Lars Bullinger Torsten Haferlach Christian Buske Vijay P.S. Rawat Michaela Feuring-Buske

Homeobox genes are key regulators in normal and malignant hematopoiesis. The human Vent-like homeobox gene VENTX, a putative homolog of the Xenopus laevis Xvent-2 gene, was shown to be highly expressed in normal myeloid cells and in patients with acute myeloid leukemia. We now demonstrate that constitutive expression of VENTX suppresses expression of genes responsible for terminal erythroid dif...

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 2001
A T Maia A M Ford G R Jalali C J Harrison G M Taylor O B Eden M F Greaves

The occurrence of childhood acute lymphoblastic leukemia (ALL) in 2 of 3 triplets provided a unique opportunity for the investigation of leukemogenesis and the natural history of ALL. The 2 leukemic triplets were monozygotic twins and shared an identical, acquired TEL-AML1 genomic fusion sequence indicative of a single-cell origin in utero in one fetus followed by dissemination of clonal progen...

Journal: :Haematologica 1999
D L Rodríguez C A López E B Cobos A J Blanco A F Fernández L F Araujo

of chromosome 3. Br J Haematol 1992; 83:158-65. 5. Shi G, Weh HJ, Dührsen U, Zeller W, Hossfeld DK. Chromosomal abnormality inv(3)(q21q26) associated with multilineage hematopoietic progenitor cells in hematopoietic malignancies. Cancer Genet Cytogenet 1997; 96:58-63. 6. Levy ER, Parganas E, Morishita K, et al. DNA rearrangements proximal to the EVI1 locus associated with the 3q21q26 syndrome. ...

Journal: :Asian Pacific journal of cancer prevention : APJCP 2010
Mustafa Kömür Fatih Erbey Ibrahim Bayram Atila Tanyeli

INTRODUCTION Acute myeloblastic leukemia (AML) accounts for 15 to 25 percent of childhood acute leukemias. The most common genetic abnormalities seen in pediatric AML patients are AML1-ETO, PML-RARα and CBFB-MYH11 genes resulting in t(8;21), t(15;17) and inv(16). These genetic defects are seen in approximately 20-25% of AML patients. OBJECTIVE We investigated in this study, incidence and prog...

Journal: :Blood 2010
Cyrus Khandanpour Christian Thiede Peter J M Valk Ehssan Sharif-Askari Holger Nückel Dietmar Lohmann Bernhard Horsthemke Winfried Siffert Andreas Neubauer Karl-Heinz Grzeschik Clara D Bloomfield Guido Marcucci Kati Maharry Marilyn L Slovak Bert A van der Reijden Joop H Jansen Hans K Schackert Khashayar Afshar Susanne Schnittger Justine K Peeters Frank Kroschinsky Gerhard Ehninger Bob Lowenberg Ulrich Dührsen Tarik Möröy

The GFI1 gene encodes a transcriptional repressor, which regulates myeloid differentiation. In the mouse, Gfi1 deficiency causes neutropenia and an accumulation of granulomonocytic precursor cells that is reminiscent of a myelodysplastic syndrome. We report here that a variant allele of GFI1 (GFI1(36N)) is associated with acute myeloid leukemia (AML) in white subjects with an odds ratio of 1.6 ...

Journal: :Blood 1996
J Jurlander M A Caligiuri T Ruutu M R Baer M P Strout A R Oberkircher L Hoffmann E D Ball D A Frei-Lahr N P Christiansen A M Block S Knuutila G P Herzig C D Bloomfield

The AML1/ETO fusion transcript is expressed in virtually all patients with t(8;21) (q22;q22) acute myeloid leukemia (AML). The fusion transcript can be detected by reverse transcription-polymerase chain reaction (RT-PCR) in most of these patients in long-term complete remission (CR) following conventional chemotherapy or autologous bone marrow transplantation (BMT). However, AML1/ETO expression...

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