Results 51 to 60 of about 2,220 (157)

Chronic eosinophilic leukemia with erythroblastic proliferation and the translocation (8;9)(p22;p24) with PCM1-JAK2 fusion gene — a new clinical, pathological and genetic entity with potential treatment target?

open access: yes, 2011
Nowotwory układu krwiotwórczego i chłonnego, powstające w wyniku translokacji t(8;9)(p21- -23;p23-24) z zaangażowaniem genów PCM1 (pericentriolar material 1) i genu JAK2 (janus- -activated kinase 2), występują bardzo rzadko.
Nowak, Grażyna   +7 more
core  

Transcriptional and Translational Products of Avian Erythroblastosis and Avian Myeloblastosis Viruses

open access: yes, 1981
The transcription and translation products of two avian acute leukemia viruses, avian erythroblastosisvirus (AEV) and avian myeloblastosisvirus (AMV), were examined.
Anderson, Steven Mathias
core   +1 more source

[Anemia and recurrences in acute lymphoblastic leukemia in children after the treatment and the frequency of the erythroblasts with micronuclei].

open access: yesActa haematologica Polonica, 1993
A retrospective analysis of the relation of relapses and anaemias to the frequency of micronucleated erythroblasts in bone marrow smear in 140 children with acute lymphoblastic leukaemia after BFM and Memphis schemes of therapy was carried out. The anaemias correlated with the frequency of micronucleated erythroblasts in statistically significant ...
K, Rytwiński   +3 more
openaire   +1 more source

IDENTIFICATION OF FREQUENT GENOMIC ABNORMALITIES IN ADULT ACUTE MYELOID LEUKEMIA PATIENTS USING SINGLE NUCLEOTIDE POLYMORPHISM ARRAYS

open access: yes, 2009
Introduction. Acute myeloid leukemia (AML) is a heterogeneous disease with various chromosomal aberrations. The karyotype at diagnosis provides important prognostic information that influences therapy and outcome of this disease.
PAOLINI, STEFANIA   +20 more
core  

SINGLE NUCLEOTIDE POLYMORPHISM (SNP) ARRAYS IDENTIFIED FREQUENT GENOMIC ABNORMALITIES IN GENES INVOLVED IN DRUG TRANSPORT AND INHIBITION OF APOPTOSIS IN ADULT ACUTE MYELOID LEUKEMIA PATIENTS

open access: yes, 2009
Introduction. Acute myeloid leukemia (AML) is a heterogeneous disease with various chromosomal aberrations. The karyotype at diagnosis provides important prognostic information that influences therapy and outcome.
F. Messa F.   +22 more
core  

Modélisation hybride de l’érythropoïèse et des maladies sanguines

open access: yes, 2011
This dissertation is devoted to the development of new methods of mathematical modeling in biology and medicine, off-lattice discrete-continuous hybrid models, and their applications to modelling of hematopoiesis and blood disorders, such as leukemia and
Kurbatova, Polina
core   +2 more sources

Genome-Wide Analysis by High-Resolution SNP Array Identifies Novel Genomic Alterations in Acute Promyelocytic Leukemia (APL).

open access: yes, 2009
Introduction: Acute promyelocytic leukemia (APL) is characterized by the chromosomal translocation t(15;17), resulting in the fusion of the promyelocytic leukemia (PML) gene and retinoic acid receptor {alpha} (RARA) gene (PML-RARA). Experimental evidence
MALAGOLA, Michele   +43 more
core  

Cell-Autonomous Upregulation of Dendritic Cell Immunocompetence Is Antigen-Dependent

open access: yes, 2005
Introduction: Dendritic cells (DCs) are the master regulators of the adaptive immune response. In previous experiments, the double-loading of DCs with matched sets of MHC class I and class II repertoires (i.e.
de Lima, Marcos   +7 more
core   +1 more source

Bone Marrow with Giant, Multinucleated RBC with Decreased Nuclear Cytoplasmic Ratio in Acute Erythroblastic Leukemia

open access: yes, 2002
BM with giant, multinucleated RBC with decreased nuclear cytoplasmic ...
Lawrence, Christine
core  

Plenary Abstracts Session & Oral Presentations

open access: yes
HemaSphere, Volume 9, Issue S1, June 2025.
wiley   +1 more source

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