[HTML][HTML] Acute myeloid leukemia with translocation t (3; 5): new molecular insights
F Dumézy, A Renneville, C Mayeur-Rousse… - …, 2013 - ncbi.nlm.nih.gov
AML with translocation t (3; 5) belongs to the “AML with myelodysplasia-related changes”
defined in the 2008 WHO classification. 1 The incidence of this balanced abnormality is less …
defined in the 2008 WHO classification. 1 The incidence of this balanced abnormality is less …
Detection of NPM/MLF1 fusion in t (3; 5)-positive acute myeloid leukemia and myelodysplasia
DA Arber, KL Chang, MH Lyda, V Bedell, R Spielberger… - Human pathology, 2003 - Elsevier
Balanced translocations are rare in myelodysplasia (MDS) and acute myeloid leukemia
(AML) with multilineage dysplasia; however, the t (3; 5)(q25; q35) and insertion variant occur …
(AML) with multilineage dysplasia; however, the t (3; 5)(q25; q35) and insertion variant occur …
Acute myeloid leukemia with associated translocation t (15; 17) and 11q23/MLL abnormality
L Campiotti, L Appio, R Casalone, R Righi… - Leukemia & …, 2008 - Taylor & Francis
The classification of acute myeloid leukemia (AML) recognizes a subgroup of diseases with
recurring genetic abnormalities. Translocation (15; 17) is the marker of acute promyelocitic …
recurring genetic abnormalities. Translocation (15; 17) is the marker of acute promyelocitic …
Translocation t (5; 18)(q35; q21) as a rare nonrandom abnormality in acute myeloid leukemia
A Daraki, LK Bourantas, KN Manola - Cytogenetic and Genome …, 2013 - karger.com
Cytogenetic abnormalities play an important role in diagnosis, classification and prognosis
in acute myeloid leukemia (AML). Nevertheless, several chromosome abnormalities have …
in acute myeloid leukemia (AML). Nevertheless, several chromosome abnormalities have …
Translocation (3; 5)(q21; q34) in erythroleukemia: a molecular and in situ hybridization study
YL Kwong - Cancer genetics and cytogenetics, 1998 - Elsevier
Translocation (3; 5) is an uncommon karyotypic aberration in acute myeloid leukemia (AML).
With the exception of M3, t (3; 5) has been reported in every other subtype of AML, being …
With the exception of M3, t (3; 5) has been reported in every other subtype of AML, being …
[HTML][HTML] NRIP3: a novel translocation partner of MLL detected in a pediatric acute myeloid leukemia with complex chromosome 11 rearrangements
MLL-rearranged acute myeloid leukemia (AML) is associated with an adverse outcome in
most treatment protocols. The MLL-gene exhibits an 8-kb breakpoint cluster region, which …
most treatment protocols. The MLL-gene exhibits an 8-kb breakpoint cluster region, which …
Altered enhancer-promoter interaction leads to MNX1 expression in pediatric acute myeloid leukemia with t (7; 12)(q36; p13)
Acute myeloid leukemia (AML) with the t (7; 12)(q36; p13) translocation occurs only in very
young children and has a poor clinical outcome. The expected oncofusion between …
young children and has a poor clinical outcome. The expected oncofusion between …
Detection of t (3; 5) and NPM1/MLF1 rearrangement in an elderly patient with acute myeloid leukemia: clinical and laboratory study with review of the literature
G Lim, JR Choi, MJ Kim, SY Kim, HJ Lee, JT Suh… - Cancer genetics and …, 2010 - Elsevier
We present a novel case of acute myeloid leukemia with an NPM1/MLF1 rearrangement in a
78-year-old Korean woman. The bone marrow chromosome study showed a complex …
78-year-old Korean woman. The bone marrow chromosome study showed a complex …
Acute myeloid leukemia with recurrent cytogenetic abnormalities
K Foucar, J Anastasi - American Journal of Clinical Pathology, 2015 - academic.oup.com
Abstract Objectives: Session 1 of the 2013 Society for Hematopathology/European
Association for Hematopathology Workshop was devoted to the cases of acute myeloid …
Association for Hematopathology Workshop was devoted to the cases of acute myeloid …
t (8; 21; 8)(p23; q22; q22): a new variant form of t (8; 21) translocation in acute myeloblastic leukemia with maturation
Y Xue, L Xu, S Chen, J Fu, Y Guo, J Li, Y Wu… - Leukemia & …, 2001 - Taylor & Francis
The complex variants of t (8; 21) involving chromosomes 8 and 21 as well as a variable
chromosome account for 1.1∼ 5% of acute myeloid leukemia (AML) patients. This paper …
chromosome account for 1.1∼ 5% of acute myeloid leukemia (AML) patients. This paper …