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Mikel P. Moyer
Observed names:
Mikel Moyer,
Mikel P Moyer,
Mikel P. Moyer
Observed institutions:
Pfizer (United States),
Epizyme (United States),
Eisai (Japan)
OpenAlex ID:
A5111682318
Selective Killing of Mixed Lineage Leukemia Cells by a Potent Small-Molecule DOT1L Inhibitor
2011
·
Scott R. Daigle
, Edward J. Olhava
, et al.
·
Cancer Cell
·
933
PDF
Durable tumor regression in genetically altered malignant rhabdoid tumors by inhibition of methyltransferase EZH2
2013
·
Sarah K. Knutson
, Natalie M. Warholic
, et al.
·
Proceedings of the National Academy of Sciences
·
810
PDF
A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells
2012
·
Sarah K Knutson
, Tim J Wigle
, et al.
·
Nature Chemical Biology
·
791
Potent inhibition of DOT1L as treatment of MLL-fusion leukemia
2013
·
Scott R. Daigle
, Edward J. Olhava
, et al.
·
Blood
·
737
A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL models
2015
·
Elayne Chan-Penebre
, Kristy G Kuplast
, et al.
·
Nature Chemical Biology
·
573
Selective Inhibition of EZH2 by EPZ-6438 Leads to Potent Antitumor Activity in EZH2 -Mutant Non-Hodgkin Lymphoma
2014
·
Sarah K. Knutson
, Satoshi Kawano
, et al.
·
Molecular Cancer Therapeutics
·
547
Anti-tumor Activity of the Type I PRMT Inhibitor, GSK3368715, Synergizes with PRMT5 Inhibition through MTAP Loss
2019
·
Andrew Fedoriw
, Satyajit R. Rajapurkar
, et al.
·
Cancer Cell
·
357
PDF
The Importance of Being Me: Magic Methyls, Methyltransferase Inhibitors, and the Discovery of Tazemetostat
2016
·
Kevin W. Kuntz
, John E. Campbell
, et al.
·
Journal of Medicinal Chemistry
·
186
Structure and Property Guided Design in the Identification of PRMT5 Tool Compound EPZ015666
2015
·
Kenneth W. Duncan
, Nathalie Rioux
, et al.
·
ACS Medicinal Chemistry Letters
·
177
Intramolecular nitrogen-hydrogen, oxygen-hydrogen and sulfur-hydrogen insertion reactions. Synthesis of heterocycles from .alpha.-diazo .beta.-keto esters
1985
·
Mikel P. Moyer
, Paul L. Feldman
, et al.
·
The Journal of Organic Chemistry
·
159
A687V EZH2 is a gain‐of‐function mutation found in lymphoma patients
2012
·
Christina R. Majer
, Lei Jin
, et al.
·
FEBS Letters
·
154
Identification of a CARM1 Inhibitor with Potent In Vitro and In Vivo Activity in Preclinical Models of Multiple Myeloma
2017
·
Allison E. Drew
, Oscar Moradei
, et al.
·
Scientific Reports
·
151
PDF
Conformational Adaptation Drives Potent, Selective and Durable Inhibition of the Human Protein Methyltransferase DOT1L
2012
·
Aravind Basavapathruni
, Lei Jin
, et al.
·
Chemical Biology & Drug Design
·
147
Metal-halogen exchange of bromoindoles. A route to substituted indoles
1986
·
Mikel P. Moyer
, John F. Shiurba
, et al.
·
The Journal of Organic Chemistry
·
147
Aryl Pyrazoles as Potent Inhibitors of Arginine Methyltransferases: Identification of the First PRMT6 Tool Compound
2015
·
Lorna H. Mitchell
, Allison E. Drew
, et al.
·
ACS Medicinal Chemistry Letters
·
145
EPZ011989, A Potent, Orally-Available EZH2 Inhibitor with Robust in Vivo Activity
2015
·
John E. Campbell
, Kevin W. Kuntz
, et al.
·
ACS Medicinal Chemistry Letters
·
131
DOT1L Inhibitor EPZ-5676 Displays Synergistic Antiproliferative Activity in Combination with Standard of Care Drugs and Hypomethylating Agents in MLL-Rearranged Leukemia Cells
2014
·
Christine R. Klaus
, Dorothy Iwanowicz
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
131
Impact of enzyme concentration and residence time on apparent activity recovery in jump dilution analysis
2011
·
Robert A. Copeland
, Aravind Basavapathruni
, et al.
·
Analytical Biochemistry
·
119
Nonclinical pharmacokinetics and metabolism of EPZ‐5676, a novel DOT1L histone methyltransferase inhibitor
2014
·
Aravind Basavapathruni
, Edward J. Olhava
, et al.
·
Biopharmaceutics & Drug Disposition
·
81
Synergistic Anti-Tumor Activity of EZH2 Inhibitors and Glucocorticoid Receptor Agonists in Models of Germinal Center Non-Hodgkin Lymphomas
2014
·
Sarah K. Knutson
, Natalie M. Warholic
, et al.
·
PLoS ONE
·
71
PDF
Small molecule inhibitors and CRISPR/Cas9 mutagenesis demonstrate that SMYD2 and SMYD3 activity are dispensable for autonomous cancer cell proliferation
2018
·
Michael J. Thomenius
, Jennifer Totman
, et al.
·
PLoS ONE
·
62
PDF
Structural Insights into Ternary Complex Formation of Human CARM1 with Various Substrates
2015
·
P. Ann Boriack-Sjodin
, Lei Jin
, et al.
·
ACS Chemical Biology
·
45
A High-Throughput Mass Spectrometry Assay Coupled with Redox Activity Testing Reduces Artifacts and False Positives in Lysine Demethylase Screening
2015
·
Tim J. Wigle
, Kerren K. Swinger
, et al.
·
SLAS DISCOVERY
·
38
PDF
Reaction Coupling between Wild-Type and Disease-Associated Mutant EZH2
2014
·
Brooke M. Swalm
, Sarah K. Knutson
, et al.
·
ACS Chemical Biology
·
35
Metabolism and disposition of the DOT1L inhibitor, pinometostat (EPZ-5676), in rat, dog and human
2015
·
Nigel J. Waters
, Sherri A. Smith
, et al.
·
Cancer Chemotherapy and Pharmacology
·
28
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Works count:
48
Citation count:
6,866
H-index:
26
I10-index:
28
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