Acute Myeloid Leukemia With t (v; 5q33) Is Associated With Poor Overall Survival and Often Lacks Myelodysplastic Features
M Yabe, G Tang, G Garcia-Manero, S Loghavi… - … Myeloma and Leukemia, 2015 - Elsevier
Background Acute myeloid leukemia (AML) with specific balanced 5q33 translocations are
classified as AML with myelodysplasia-related changes regardless of their morphologic …
classified as AML with myelodysplasia-related changes regardless of their morphologic …
[HTML][HTML] Aberrant MNX1 expression associated with t (7; 12)(q36; p13) pediatric acute myeloid leukemia induces the disease through altering histone methylation
A Waraky, A Östlund, T Nilsson, D Weichenhan… - …, 2024 - ncbi.nlm.nih.gov
Certain subtypes of acute myeloid leukemia (AML) in children have inferior outcome, such
as AML with translocation t (7; 12)(q36; p13) leading to an MNX1:: ETV6 fusion along with …
as AML with translocation t (7; 12)(q36; p13) leading to an MNX1:: ETV6 fusion along with …
[PDF][PDF] A Novel Three Way Translocation in a Child with t (8: 21) Acute Myeloid Leukemia (AML-M2) Involving 6q27 with Loss of Y chromosome.
M Ramzan, M Lukman, M Singh, S Katewa - 2018 - apjpch.com
Case Study Page 1 P age | 41 www.apjpch.com Asia Pac J Paediatr Child Health Volume 2,
October-December 2018 Case Study A Novel Three Way Translocation in a Child with t(8:21) …
October-December 2018 Case Study A Novel Three Way Translocation in a Child with t(8:21) …
[HTML][HTML] Acute Myeloid Leukemia with t (6; 9)(p23; q34) Is Associated Poor Outcome in Childhood AML Regardless of FLT3/ITD Status, A Report From Children's …
PP Moraleda, TA Alonzo, RB Gerbing, SC Raimondi… - Blood, 2012 - Elsevier
Abstract Abstract 2541 Translocation t (6; 9) is a rare recurring cytogenetic aberration
resulting in the formation of a chimeric fusion gene, DEK-NUP214 (previously known as …
resulting in the formation of a chimeric fusion gene, DEK-NUP214 (previously known as …
t(3;21)(q26;q22) with AML1 rearrangement in a de novo childhood acute monoblastic leukaemia
B Johansson, T Fioretos, S Garwicz… - British journal of …, 1996 - Wiley Online Library
t (3; 21)(q26; q22) is a recurrent chromosomal abnormality in Philadelphia‐positive chronic
myeloid leukaemia in blast crisis and in treatment‐related myelodysplastic syndrome and …
myeloid leukaemia in blast crisis and in treatment‐related myelodysplastic syndrome and …
Acute Myeloid Leukemia with t (6; 9)(P23; Q34): Case Report
R Lasan Trčić, I Kardum-Skelin, Z Šiftar… - … European Congress of …, 2012 - croris.hr
Aim: The translocation (6; 9)(p23; q34) is a rare cytogenetic aberration found in patients with
acute myeloid leukemia (AML)(about 1% of all AML), and correlates with poor clinical …
acute myeloid leukemia (AML)(about 1% of all AML), and correlates with poor clinical …
Prognostic implications of t (10; 11) translocations in childhood acute myelogenous leukemia: a report from the Children's Cancer Group
JN Casillas, WG Woods, SP Hunger… - Journal of pediatric …, 2003 - journals.lww.com
Purpose: This was a retrospective analysis of outcome based on cytogenetics for a
Children's Cancer Group phase 3 trial of acute myelogenous leukemia (AML)(CCG-2891) …
Children's Cancer Group phase 3 trial of acute myelogenous leukemia (AML)(CCG-2891) …
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 …
Acute Myeloid Leukemia (AML) with t (6; 9)(p23; q34) Defines a Very Poor Risk Leukemia Subgroup with Distinguishing Clinicopathological Features: A United States …
ML Slovak, CD Bloomfield, H Gundacker, G Dewald… - Blood, 2004 - Elsevier
Abstract The t (6; 9)(p23; q34) translocation, which results in the formation of a chimeric
fusion gene DEK/CAN on the der (6) chromosome, is a rare recurring cytogenetic aberration …
fusion gene DEK/CAN on the der (6) chromosome, is a rare recurring cytogenetic aberration …
Identification of t (15; 17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2
S Li, L Zhang, WF Kern, D Andrade, JE Forsberg… - Cancer genetics and …, 2002 - Elsevier
A 32-year-old man was newly diagnosed with acute myelocytic leukemia, classified as acute
myeloblastic leukemia with maturation (AML-M2) according to the French–American–British …
myeloblastic leukemia with maturation (AML-M2) according to the French–American–British …