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RUNX1T1 gene

Known as: ETO, RUNX1T1, RUNX1, TRANSLOCATED TO, 1 
This gene plays a role in transcriptional regulation and hematopoiesis.
National Institutes of Health

Papers overview

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2007
2007
The 8;21 chromosomal translocation occurs in 15% to 40% of patients with the FAB M2 subtype of acute myeloid leukemia (AML). This… 
2004
2004
Translocation t(8;21)(q22;q22) is a common karyotypic abnormality detected in about 15% of acute myeloid leukemia (AML) cases… 
Highly Cited
2001
Highly Cited
2001
AML1-MTG8 chimeric oncogene is generated in acute myelogenous leukemia with t(8;21), and seems to be responsible for the… 
2001
2001
We report a case of acute myeloblastic leukemia (AML)-M2 (by French-American-British classification) with t(8;21) (q22;q22) that… 
2000
2000
Abstract: We evaluated the usefulness of a recently developed real‐time reverse transcriptase polymerase chain reaction (RT‐PCR… 
1998
1998
The t(8;21) translocation associated with acute myeloid leukemia (AML) disrupts two genes, the AML1 gene also known as the core… 
1995
1995
The t(8; 21) is a common chromosomal abnormality, preferentially associated with acute leukemia showing features of myeloid… 
1994
1994
In the t(8;21) of acute myeloid leukemia (AML) M2, breakpoints are clustered on both chromosomes. The chromosome 21 breakpoint…