Search Results - "Mohammadhosseini, Mona"
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Abstract 531: Disruption of a histone chaperone pathway delays inflammation-driven AML progression
Published in Cancer research (Chicago, Ill.) (01-07-2021)“…Abstract Background: Inflammation plays a crucial role in normal and malignant hematopoiesis. Patients with acute myeloid leukemia (AML) exhibit aberrant…”
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3021 – A NOVEL HISTONE CHAPERONE PATHWAY DRIVES IL-1β-MEDIATED AML PROGRESSION
Published in Experimental hematology (01-08-2020)“…Genetic heterogeneity remains an ongoing challenge in treating acute myeloid leukemia (AML). Identifying microenvironment-driven pathways that are active…”
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The TLK-ASF1 histone chaperone pathway plays a critical role in IL-1β–mediated AML progression
Published in Blood (27-06-2024)“…•TLK and ASF1 levels are elevated in patients with AML across genetic subtypes and upregulated by IL-1β–mediated inflammatory stress.•Targeting TLK2 or ASF1B…”
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Investigating effect of ferric stearate on stabilization efficiency of a phenolic antioxidant during thermal oxidation of polyethylene
Published in Iranian polymer journal (01-10-2014)“…This study aimed to achieve a formulation for an additive to produce oxo-biodegradable films that accelerates oxidative degradation of the films after…”
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3093 – CHRONIC IL1Β INDUCED STRESS DRIVES EXPANSION OF TET2 DEFICIENT PROGENITORS THROUGH ENHANCED SELF-RENEWAL ABILITY
Published in Experimental hematology (01-08-2021)“…Clonal hematopoiesis (CH) increases the risk for the development of myeloid malignancies. Inflammation plays a substantial role in leukemia progression;…”
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Targeting CCL2/CCR2 Signaling Overcomes MEK Inhibitor Resistance in Acute Myeloid Leukemia
Published in Clinical cancer research (15-05-2024)“…Emerging evidence underscores the critical role of extrinsic factors within the microenvironment in protecting leukemia cells from therapeutic interventions,…”
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3024 – GERMLINE RUNX1 MUTATIONS -MEDIATED CHANGES COOPERATES WITH INFLAMMATORY MICROENVIRONMENT TO DRIVE DEFECTIVE HEMATOPOIESIS IN FAMILIAL PLATELET DISORDER
Published in Experimental hematology (01-08-2021)“…Familial platelet disorder (FPD) is caused by heterozygous germline mutations in RUNX1. FPD individuals have defective platelet functions and increased risk of…”
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Runx1-R188Q germ line mutation induces inflammation and predisposition to hematologic malignancies in mice
Published in Blood advances (12-12-2023)“…Germ line mutations in the RUNX1 gene cause familial platelet disorder (FPD), an inherited disease associated with lifetime risk to hematopoietic malignancies…”
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