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Publications by Sylvain Mareschal
Mediation Analysis Reveals Common Mechanisms of RUNX1 Point Mutations and RUNX1/RUNX1T1 Fusions Influencing Survival of Patients With Acute Myeloid Leukemia
Scientific Reports
Multidisciplinary
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Identification of Key Genes and Pathways Associated With RUNX1 Mutations in Acute Myeloid Leukemia Using Bioinformatics Analysis
Medical Science Monitor
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A Minicircuitry of microRNA-9-1 and RUNX1-RUNX1T1 Contributes to Leukemogenesis in T(8;21) Acute Myeloid Leukemia
International Journal of Cancer
Cancer Research
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Paradoxical Enhancement of Leukemogenesis in Acute Myeloid Leukemia With Moderately Attenuated RUNX1 Expressions
Blood advances
Hematology
Structural and Functional Characterization of Runx1 Point Mutations Identified in Leukemia and Cleidocranial Dysplasia Patients.
High Expression of RUNX1 Is Associated With Poorer Outcomes in Cytogenetically Normal Acute Myeloid Leukemia
Oncotarget
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RUNX1 Deficiency (Familial Platelet Disorder With Predisposition to Myeloid Leukemia, FPDMM)
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A Three-miRNA-Based Expression Signature at Diagnosis Can Predict Occurrence of Relapse in Children With T(8;21) RUNX1 -RUNX1T1 Acute Myeloid Leukaemia
British Journal of Haematology
Hematology
The Sensitivity of Human Cells Expressing RUNX1-RUNX1T1 to Chemotherapeutic Agents
Leukemia
Cancer Research
Oncology
Anesthesiology
Pain Medicine
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Cdk6 Blocks Myeloid Differentiation by Interfering With Runx1 DNA Binding and Runx1-C/EBPα Interaction
EMBO Journal
Immunology
Molecular Biology
Biochemistry
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Neuroscience
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Genetics