نتایج جستجو برای: acute myeloid leukemia pediatrics

تعداد نتایج: 717874  

Journal: :Haematologica 2008
Elisabeth Walsby Val Walsh Chris Pepper Alan Burnett Ken Mills

BACKGROUND Aurora kinases play an essential role in the orchestration of chromosome separation and cytokinesis during mitosis. Small-molecule inhibition of the aurora kinases has been shown to result in inhibition of cell division, phosphorylation of histone H3 and the induction of apoptosis in a number of cell systems. These characteristics have led aurora kinase inhibitors to be considered as...

Mehdi Allahbakhshian Farsani, Mohammad Hossein Mohammadi, Seyed Hossein Abtahi,

Background: Acute myeloid leukemia (AML) is characterized by the proliferation of myeloid precursors and abnormal differentiation of hematopoietic stem cells, which results in the accumulation of immature cells in the bone marrow (BM). The accumulation of these cells in the bone marrow causes molecular and cellular changes in the microenvironment of the bone marrow. The adiponectin hormone orig...

Journal: :Haematologica 2010
Sabina Chiaretti Monica Messina Simona Tavolaro Giuseppe Zardo Loredana Elia Antonella Vitale Alessandro Fatica Paolo Gorello Alfonso Piciocchi Gina Scappucci Irene Bozzoni Claudio Fozza Anna Candoni Anna Guarini Robin Foà

BACKGROUND Until recently, few molecular aberrations were recognized in acute lymphoblastic leukemia of T-cell origin; novel lesions have recently been identified and a certain degree of overlap between acute myeloid leukemia and T-cell acute lymphoblastic leukemia has been suggested. To identify novel T-cell acute lymphoblastic leukemia entities, gene expression profiling was performed and cli...

Journal: :Haematologica 2011
Brian V Balgobind Marry M Van den Heuvel-Eibrink Renee X De Menezes Dirk Reinhardt Iris H I M Hollink Susan T J C M Arentsen-Peters Elisabeth R van Wering Gertjan J L Kaspers Jacqueline Cloos Evelien S J M de Bont Jean-Michel Cayuela Andre Baruchel Claus Meyer Rolf Marschalek Jan Trka Jan Stary H Berna Beverloo Rob Pieters C Michel Zwaan Monique L den Boer

BACKGROUND Pediatric acute myeloid leukemia is a heterogeneous disease characterized by non-random genetic aberrations related to outcome. The genetic subtype is currently detected by different diagnostic procedures which differ in success rate and/or specificity. DESIGN AND METHODS We examined the potential of gene expression profiles to classify pediatric acute myeloid leukemia. Gene expres...

2013
Jeremy B. Moad Kellie R. Jones

Extrinsic compression of the pulmonary arteries by mediastinal masses, while rare, is the most common cause of non-congenital peripheral pulmonary artery stenosis. Granulocytic myeloid sarcomas are an extramedullary manifestation of acute myeloid leukemia, with a wide variability in their presentation. They can present either de novo as soft tissue masses or in conjunction with acute myeloid le...

2013
Luzia Beatriz Ribeiro Zago Antônio Alexandre Lisbôa Ladeia Renata Margarida Etchebehere Leonardo Rodrigues de Oliveira

Myeloid sarcomas are extramedullary solid tumors composed of immature granulocytic precursor cells. In association with acute myeloid leukemia and other myeloproliferative disorders, they may arise concurrently with compromised bone marrow related to acute myeloid leukemia, as a relapsed presentation, or occur as the first manifestation. The testicles are considered to be an uncommon site for m...

Journal: :Haematologica 2007
David P Steensma

Acute Myeloid Leukemia 753-762 Arsenic trioxide induces accumulation of cytotoxic levels of ceramide in acute promyelocytic leukemia and adult T-cell leukemia/lymphoma cells through de novo ceramide synthesis and inhibition of glucosylceramide synthase activity Ghassan S. Dbaibo, Youmna Kfoury, Nadine Darwiche, Shoghag Panjarian, Lina Kozhaya, Rihab Nasr, Mazen Abdallah, Olivier Hermine, Marwan...

Background: Several studies have examined the presence of DNA methylation of CpG islands in leukemia. Methylation of SOX17 and RUNX3 genes may play a role in leukemogenesis through silencing tumor suppressor genes. We investigated the methylation status of SOX17 and RUNX3 genes in patients with acute leukemia.    Methods: In this case-control study, peripheral blood samples from 100 AML and 10...

Journal: :Blood 1985
P B Neame P Soamboonsrup G Browman R D Barr N Saeed B Chan M Pai A Benger W E Wilson I R Walker

Acute mixed myeloid-lymphoid leukemia is uncommon. We report four cases in which myeloid and lymphoid cell markers were observed simultaneously or sequentially when 94 patients with acute leukemia were phenotyped according to the French-American-British (FAB) classification system, with cytochemical stains, and with immunologically defined differentiation markers (identified by monoclonal antib...

Journal: :Haematologica 2011
Iris H I M Hollink Marry M van den Heuvel-Eibrink Susan T C J M Arentsen-Peters Martin Zimmermann Justine K Peeters Peter J M Valk Brian V Balgobind Edwin Sonneveld Gertjan J L Kaspers Eveline S J M de Bont Jan Trka Andre Baruchel Ursula Creutzig Rob Pieters Dirk Reinhardt C Michel Zwaan

BACKGROUND Dysfunctioning of CCAAT/enhancer binding protein α (C/EBPα) in acute myeloid leukemia can be caused, amongst others, by mutations in the encoding gene (CEBPA) and by promoter hypermethylation. CEBPA-mutated acute myeloid leukemia is associated with a favorable outcome, but this may be restricted to the case of double mutations in CEBPA in adult acute myeloid leukemia. In pediatric ac...

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