604. Molecular Pharmacology and Drug Resistance: Myeloid Neoplasms: Poster III
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DYRK1A interacts with EZH2 to regulate transcriptionally active chromatin in myeloid leukemia associated with down syndrome
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DYRK1A interacts with EZH2 to regulate transcriptionally active chromatin in myeloid leukemia associated with down syndrome
BTK regulates EZH2 stability in myeloid leukemia associated with down syndrome
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BTK regulates EZH2 stability in myeloid leukemia associated with down syndrome
Adaptive rebalancing of ROS composition averts LSD1 inhibitor–induced oxidative stress in AML
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Adaptive rebalancing of ROS composition averts LSD1 inhibitor–induced oxidative stress in AML
Single‑cell analysis of BAX responses reveals venetoclax sensitivity and enables development of BAX‑targeting combinations in AML
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Single‑cell analysis of BAX responses reveals venetoclax sensitivity and enables development of BAX‑targeting combinations in AML
Distinct mTOR and CDK1 regulated translation circuits sustain FLT3 mutated AML survival under therapy
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Distinct mTOR and CDK1 regulated translation circuits sustain FLT3 mutated AML survival under therapy
BPI 2358 reprograms immunosuppressive macrophages and impairs leukemic progression in MN1 overexpressing AML In Vivo
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BPI 2358 reprograms immunosuppressive macrophages and impairs leukemic progression in MN1 overexpressing AML In Vivo
METTL3 inhibition disrupts R loop homeostasis and activates the cgas sting pathway in Acute Myeloid Leukemia
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METTL3 inhibition disrupts R loop homeostasis and activates the cgas sting pathway in Acute Myeloid Leukemia
Co targeting menin and RAS in KMT2A r NPM1c AML with activated RTK RAS MAPK signaling
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Co targeting menin and RAS in KMT2A r NPM1c AML with activated RTK RAS MAPK signaling
Anti leukemic efficacy of a novel inhibitor for KMT2A r FLT3 driven AML via multi kinase targeting and synergy with menin inhibition
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Anti leukemic efficacy of a novel inhibitor for KMT2A r FLT3 driven AML via multi kinase targeting and synergy with menin inhibition
TGM2 as a novel therapeutic target in venetoclax resistant AML Disrupting histone serotonylation driven mitophagy with nanoparticle delivered inhibitors
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TGM2 as a novel therapeutic target in venetoclax resistant AML Disrupting histone serotonylation driven mitophagy with nanoparticle delivered inhibitors
Synergistic correction of polycythemia vera phenotype via dual targeting of JAK2 and Gas6 in Jak2 exon 12 mutant mice
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Synergistic correction of polycythemia vera phenotype via dual targeting of JAK2 and Gas6 in Jak2 exon 12 mutant mice
Inhibition of Drp1 a mitochondrial fission GTPase disrupts mitochondrial quality control and impairs stem like properties in Acute Myeloid Leukemia
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Inhibition of Drp1 a mitochondrial fission GTPase disrupts mitochondrial quality control and impairs stem like properties in Acute Myeloid Leukemia
Preclinical efficacy of dual BET HAT inhibitor–based combinations against post myeloproliferative neoplasm secondary AML cells
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Preclinical efficacy of dual BET HAT inhibitor–based combinations against post myeloproliferative neoplasm secondary AML cells
CD123 targeted radiotheranostics of Acute Myeloid Leukemia with 89Zr 177Lu labeled pivekimab
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CD123 targeted radiotheranostics of Acute Myeloid Leukemia with 89Zr 177Lu labeled pivekimab
ORM 1153 A CD123 targeting degrader antibody conjugate with GSPT1 degrading payload exhibits potent preclinical antitumor activity in Acute Myeloid Leukemia
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ORM 1153 A CD123 targeting degrader antibody conjugate with GSPT1 degrading payload exhibits potent preclinical antitumor activity in Acute Myeloid Leukemia
FLT3 F691L confers kinase independent resistance via Grb2 dependent MAPK signaling in AML
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FLT3 F691L confers kinase independent resistance via Grb2 dependent MAPK signaling in AML
CBX–663 a novel TCR mimetic T cell engager targeting a telomerase reverse transcriptase TERT peptide HLA complex that exhibits potent efficacy against AML cells
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CBX–663 a novel TCR mimetic T cell engager targeting a telomerase reverse transcriptase TERT peptide HLA complex that exhibits potent efficacy against AML cells
Bioequivalence of ruxolitinib once daily extended release vs twice daily immediate release tablets in healthy adults
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Bioequivalence of ruxolitinib once daily extended release vs twice daily immediate release tablets in healthy adults
First in human randomized placebo controlled Phase 1 study of RPT1G a novel hyperbolic NAMPT inhibitor for use in acute leukemias Safety pharmacokinetics and pharmacodynamics in healthy volunteers
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First in human randomized placebo controlled Phase 1 study of RPT1G a novel hyperbolic NAMPT inhibitor for use in acute leukemias Safety pharmacokinetics and pharmacodynamics in healthy volunteers
The impact of NR1I2 gene polymorphism and body weight on asciminib pharmacokinetics in patients with chronic myeloid leukemia
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The impact of NR1I2 gene polymorphism and body weight on asciminib pharmacokinetics in patients with chronic myeloid leukemia