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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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Highly Cited
2014
Highly Cited
2014
The role of Fat Mass and Obesity-associated protein (FTO) and its substrate N6-methyladenosine (m6A) in mRNA processing and… 
Highly Cited
2003
Highly Cited
2003
The t(8;21)(q22;q22) translocation, occurring in 40% of patients with acute myeloid leukemia (AML) of the FAB-M2 subtype (AML… 
Highly Cited
2000
Highly Cited
2000
Dentato-rubral and pallido-luysian atrophy (DRPLA) is one of the family of neurodegenerative diseases caused by expansion of a… 
Highly Cited
1998
Highly Cited
1998
ABSTRACT Nuclear receptor corepressor (CoR)-histone deacetylase (HDAC) complex recruitment is indispensable for the biological… 
Highly Cited
1998
Highly Cited
1998
The AML1 transcription factor and the transcriptional coactivators p300 and CBP are the targets of chromosome translocations… 
Highly Cited
1998
Highly Cited
1998
Gene PRAME was found to encode an antigen recognized on a human melanoma cell line by an autologous cytolytic T‐lymphocyte clone… 
Highly Cited
1998
Highly Cited
1998
The t(16;21)(q24;q22) translocation is a rare but recurrent chromosomal abnormality associated with therapy-related myeloid… 
Highly Cited
1998
Highly Cited
1998
ABSTRACT The AML1-CBFβ transcription factor complex is essential for the definitive hematopoiesis of all lineages and is the most… 
Highly Cited
1993
Highly Cited
1993
The t(8;21) translocation is one of the most frequent chromosome abnormalities in acute myeloid leukemia. It has been shown that… 
Highly Cited
1993
Highly Cited
1993
The 8;21 translocation is one of the most common chromosomal translocations in acute myelogenous leukemia (AML), accounting for…