AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
about
Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia-7/7q- syndrome in myeloid-lineage hematopoietic malignancies: attempts to understand this complex disease entity.Posttranslational modifications of RUNX1 as potential anticancer targets.Role of RUNX1 in hematological malignancies.Modeling Myeloid Malignancies Using Zebrafish.
P2860
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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name
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
@en
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
@nl
type
label
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
@en
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
@nl
prefLabel
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
@en
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
@nl
P2093
P2860
P356
P1476
AML1/RUNX1 gene point mutations in childhood myeloid malignancies.
@en
P2093
Alexandr Migas
Natallia Savva
Olga Mishkova
Olga V Aleinikova
P2860
P304
P356
10.1002/PBC.22980
P577
2011-02-03T00:00:00Z