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Role of RUNX1 in hematological malignancies
R Sood, Y Kamikubo, P Liu - … Journal of the American Society of …, 2017 - ashpublications.org
RUNX1 is a member of the core-binding factor family of transcription factors and is
indispensable for the establishment of definitive hematopoiesis in vertebrates. RUNX1 is …
indispensable for the establishment of definitive hematopoiesis in vertebrates. RUNX1 is …
[HTML][HTML] RUNX transcription factors: orchestrators of development
ABSTRACT RUNX transcription factors orchestrate many different aspects of biology,
including basic cellular and developmental processes, stem cell biology and tumorigenesis …
including basic cellular and developmental processes, stem cell biology and tumorigenesis …
Dnmt3a is essential for hematopoietic stem cell differentiation
Loss of the de novo DNA methyltransferases Dnmt3a and Dnmt3b in embryonic stem cells
obstructs differentiation; however, the role of these enzymes in somatic stem cells is largely …
obstructs differentiation; however, the role of these enzymes in somatic stem cells is largely …
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants
Standardized variant curation is essential for clinical care recommendations for patients with
inherited disorders. Clinical Genome Resource (ClinGen) variant curation expert panels are …
inherited disorders. Clinical Genome Resource (ClinGen) variant curation expert panels are …
Runx transcription factors in the development and function of the definitive hematopoietic system
M de Bruijn, E Dzierzak - Blood, The Journal of the American …, 2017 - ashpublications.org
The Runx family of transcription factors (Runx1, Runx2, and Runx3) are highly conserved
and encode proteins involved in a variety of cell lineages, including blood and blood-related …
and encode proteins involved in a variety of cell lineages, including blood and blood-related …
Secondary leukemia in patients with germline transcription factor mutations (RUNX1, GATA2, CEBPA)
Recognition that germline mutations can predispose individuals to blood cancers, often
presenting as secondary leukemias, has largely been driven in the last 20 years by studies …
presenting as secondary leukemias, has largely been driven in the last 20 years by studies …
RUNX1 isoform disequilibrium promotes the development of trisomy 21–associated myeloid leukemia
Abstract Gain of chromosome 21 (Hsa21) is among the most frequent aneuploidies in
leukemia. However, it remains unclear how partial or complete amplifications of Hsa21 …
leukemia. However, it remains unclear how partial or complete amplifications of Hsa21 …
Xenograft models for normal and malignant stem cells
S Goyama, M Wunderlich… - Blood, The Journal of the …, 2015 - ashpublications.org
The model systems available for studying human hematopoiesis, malignant hematopoiesis,
and hematopoietic stem cell (HSC) function in vivo have improved dramatically over the last …
and hematopoietic stem cell (HSC) function in vivo have improved dramatically over the last …
Specification and function of hemogenic endothelium during embryogenesis
E Gritz, KK Hirschi - Cellular and Molecular Life Sciences, 2016 - Springer
Hemogenic endothelium is a specialized subset of develo** vascular endothelium that
acquires hematopoietic potential and can give rise to multilineage hematopoietic stem and …
acquires hematopoietic potential and can give rise to multilineage hematopoietic stem and …
Diverse epigenetic mechanisms of human disease
Epigenetic control of gene expression programs is essential for normal organismal
development and cellular function. Abrogation of epigenetic regulation is seen in many …
development and cellular function. Abrogation of epigenetic regulation is seen in many …