نتایج جستجو برای: acute myeloid leukemia
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RUNX1 gene alterations are associated with acquired and inherited hematologic malignancies that include familial platelet disorder/acute myeloid leukemia, primary or secondary acute myeloid leukemia, and chronic myelomonocytic leukemia. Recently, we reported that RUNX1-mediated silencing of nonmuscle myosin heavy chain IIB (MYH10) was required for megakaryocyte ploidization and maturation. Here...
24Boyse, E. A., L. J. Old, G. Geering, and E. Stockert, unpublished observations. 25 Cells from 4 cases of human leukemia (acute leukemia in a child, acute myeloid leukemia, chronic myeloid leukemia, and chronic lymphatic leukemia) were obtained through the courtesy of Dr. B. Clarkson, Dr. L. Murphy, and Dr. C. Tan of Sloan-Kettering Institute. These cells did not acquire sensitivity to Rausche...
Patient Selection Criteria Coverage eligibility will be considered for allogeneic hematopoietic cell transplant (allo-HCT) using a myeloablative conditioning (MAC) regimen to treat acute myeloid leukemia (AML) when ANY of the following criteria are met: Poorto intermediaterisk acute myeloid leukemia (AML) in first complete remission (CR1) (see Policy Guidelines section for information on risk...
BACKGROUND Several studies of pediatric acute myeloid leukemia have described the various type-I or type-II aberrations and their relationship with clinical outcome. However, there has been no recent comprehensive overview of these genetic aberrations in one large pediatric acute myeloid leukemia cohort. DESIGN AND METHODS We studied the different genetic aberrations, their associations and t...
BACKGROUND We highlight the orbital manifestations of acute myeloid leukemia and the role of peripheral blood smear in the diagnosis of these cases. A total of 12 patients who presented with proptosis and were subsequently diagnosed to have acute myeloid leukemia based on incision biopsy or peripheral blood smear were included in the study. RESULTS A retrospective review of all cases of acute...
Allogeneic blood or marrow hematopoietic cell transplantation continues to be the most potent anti-leukemic treatment for adult patients with standard, high-risk, or chemo-refractory acute myeloid leukemia. Until recently, this procedure was generally limited to those recipients who had an available matched-sibling donor or matched-unrelated donor. Technical advances in graft cell processing an...
Genomic studies of hematologic malignancies have identified a spectrum of recurrent somatic alterations that contribute to acute myeloid leukemia initiation and maintenance, and which confer sensitivities to molecularly targeted therapies. The majority of these genetic events are small, site-specific alterations in DNA sequence. In more than two thirds of patients with de novo acute myeloid leu...
In acute myeloid leukemia, there is growing evidence for splicing pattern deregulation, including differential expression of linear splice isoforms of the commonly mutated gene nucleophosmin (NPM1). In this study, we detect circular RNAs of NPM1 and quantify circRNA hsa_circ_0075001 in a cohort of NPM1 wild-type and mutated acute myeloid leukemia (n=46). Hsa_circ_0075001 expression correlates p...
Myeloid sarcoma is a rare tumor mass with extra medullary growth pattern, composed of myeloblast or immature myeloid cells. (MS) distinct clinical presentation acute leukemia (AML) where less than 1% patients present prominent disease which most commonly involves the bone, skin, lymph node, soft tissues, gastrointestinal tract testes. The recommended treatment regimen in isolated bone marrow in...
Background: Interaction between killer cell immunoglobulin-like receptors (KIR) and human leukocyte antigen (HLA) class I molecules is important for regulation of natural killer (NK) cell function. Objective: The aim of this study was to investigate the impact of compound KIR-HLA genotype on susceptibility to acute leukemia. Methods: Cohorts of Iranian patients with acute myeloid leukemia (AML;...
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