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RUNX1 gene
Known as:
PEBP2A2
, AMLCR1
, RUNX1
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This gene plays a role in transcriptional regulation and cytogenetic aberrations are associated with several leukemias.
National Institutes of Health
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Related topics
Related topics
10 relations
AML1-ETO Fusion Protein Expression
EVI1-AML1 Fusion Protein Expression
Homo sapiens
REL gene
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RUNX1 wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Co-Occurrence of Platelet Dysfunction , Myeloid Malignancy and IgA Deficiency in a Family with a Novel RUNX 1 Mutation
Caitlin O'Neill
,
Imran Siddiqi
,
S. Gruber
,
K. McDonnell
,
S. Moayeri
,
C. O'Connell
2017
Corpus ID: 33619861
Familial platelet disorder with propensity for myeloid malignancy (FPD/AML), an autosomal dominant disorder associated with…
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2015
2015
Genetic Analysis of Gata3 and Runx1 in Mammary Tumor Formation
Nayasta Ademmana Kusdaya
2015
Corpus ID: 56250273
Genomic analysis of breast cancer (BC) has revealed the existence of recurrent copy number losses and mutations in GATA3 and…
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2005
2005
AMLI a but not AMLI b Inhibits Erythroid Differentiation Induced by Sodium Butyrate and Enhances the Megakaryocytic Differentiation of K 562 Leukemia Cells 1
N. Niitsu
,
Y. Yamamoto-Yamaguchi
,
+4 authors
Y. Honma
2005
Corpus ID: 28586351
AMLI may play a role in growth and differentiation of cells along erythroid and/or megakaryocytic lineages, because a significant…
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