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t(8;21)

A cytogenetic abnormality that involves a translocation between chromosomes 8 and 21.
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
We aimed to improve the outcome of t(8;21) acute myeloid leukemia (AML) in the first complete remission (CR1) by applying risk… 
Highly Cited
2006
Highly Cited
2006
The t(8;21)(q22;q22) translocation is one of the most common genetic abnormalities in acute myeloid leukemia (AML), identified in… 
Highly Cited
2003
Highly Cited
2003
The transcription factor PU.1 plays a pivotal role in normal myeloid differentiation. PU.1(-/-) mice exhibit a complete block in… 
Highly Cited
2001
Highly Cited
2001
ABSTRACT t(8;21) and t(16;21) create two fusion proteins, AML-1–ETO and AML-1–MTG16, respectively, which fuse the AML-1 DNA… 
Highly Cited
2000
Highly Cited
2000
Leukemia-specific AML1/ETO transcripts are detectable in most patients with t(8;21) acute myelogenous leukemia (AML) in long-term… 
Review
1999
Review
1999
PURPOSE To examine the effect of single compared with repetitive (at least three) cycles of high-dose cytarabine after induction… 
Highly Cited
1998
Highly Cited
1998
The t(8;21) translocation between two genes known as AML1 and ETO is seen in approximately 12-15% of all acute myeloid leukemia… 
Highly Cited
1991
Highly Cited
1991
The t(8;21)(q22;q22) translocation is a non-random chromosomal abnormality frequently found in patients with acute myeloid…