Mary Pat Beavers - Concepedia

Author

Mary Pat Beavers

Johnson & Johnson (United States)

Also Known As

Beavers, M.P., M P Beavers, Mary Pat Beavers

Publications

885

Citations

H-Index

Concepts

All Affiliations

Johnson & Johnson (United States)University of Minnesota University of Pennsylvania Twin Cities Orthopedics

About

Mary Pat Beavers is an author at Johnson & Johnson (United States) specializing in medicine, natural sciences, and drug discovery.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	461
2	Natural Sciences	9	9	427
3	Biochemistry	9	9	326
4	Engineering	1	1	25
5	Health Sciences	1	1	28

Mary Pat Beavers

Publications

855

Citations

H-Index

Page 1

	Year	Citations
Antibody modeling assessment Juan C. Almagro, Mary Pat Beavers, Francisco G. Hernandez-Guzman, Proteins Structure Function and Bioinformatics Immunoglobulin StructureBiomolecular Structure PredictionImmunologyMolecular BiologyImmunotherapy	2011	129
Small-molecule inhibitors of integrin α <sub>2</sub> β <sub>1</sub> that prevent pathological thrombus formation via an allosteric mechanism Meredith W. Miller, Sandeep Basra, Daniel W. Kulp, Proceedings of the National Academy of Sciences	2009	86
Synthesis and Discovery of Macrocyclic Polyoxygenated Bis-7-azaindolylmaleimides as a Novel Series of Potent and Highly Selective Glycogen Synthase Kinase-3β Inhibitors Gee‐Hong Kuo, Catherine Prouty, A. DeAngelis, Journal of Medicinal Chemistry Combinatorial ChemistryMedicinal ChemistryMacrocyclic MaleimidesNovel SeriesBiochemistry	2003	82
Synthesis and evaluation of 3-anilino-quinoxalinones as glycogen phosphorylase inhibitors Joseph Dudash, Yong‐Zheng Zhang, John B. Moore, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryMedicineGlycogen Phosphorylase InhibitorsPharmacologyPharmaceutical Chemistry	2005	77
Metastin (KiSS-1) Mimetics Identified from Peptide Structure−Activity Relationship-Derived Pharmacophores and Directed Small Molecule Database Screening Michael J. Orsini, Mark Klein, Mary Pat Beavers, Journal of Medicinal Chemistry	2007	76
The Total Synthesis of Roquefortine C and a Rationale for the Thermodynamic Stability of Isoroquefortine C over Roquefortine C Ning Shangguan, Warren J. Hehre, William Ohlinger, Journal of the American Chemical Society Combinatorial ChemistryAsymmetric CatalysisMedicinal ChemistryRoquefortine C StructureIsoroquefortine C	2008	48
Kinetic Characterization and Molecular Docking of a Novel, Potent, and Selective Slow-Binding Inhibitor of Human Cathepsin L Parag P. Shah, Michael C. Myers, Mary Pat Beavers, Molecular Pharmacology	2008	44
Nonpeptidic, Noncovalent Inhibitors of the Cysteine Protease Cathepsin S Robin L. Thurmond, Mary Pat Beavers, Hui Cai, Journal of Medicinal Chemistry Protein ChemistryMedicinal ChemistryProgram DockBiochemistryDrug Discovery Effort	2004	36
Synthesis and biological evaluation of novel macrocyclic bis-7-azaindolylmaleimides as potent and highly selective glycogen synthase kinase-3β (GSK-3β) inhibitors Lan Shen, Catherine Prouty, Barbara R. Conway, Bioorganic & Medicinal Chemistry Molecular PharmacologyMedicinal ChemistryBiochemistryMedicineNatural Sciences	2004	34
Design and Evaluation of Nonpeptide Fibrinogen .gamma. Chain-Based GPIIB/IIIA Antagonists William J. Hoekstra, Mary Pat Beavers, Patricia Andrade‐Gordon, Journal of Medicinal Chemistry	1995	34

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