John R. Omnaas - Concepedia

Author

John R. Omnaas

University of Michigan

Also Known As

J R Omnaas, J. R. OMNAAS, J. R. Omnaas, J.R. Omnaas, JOHN R. OMNAAS, John Omnaas, John R. Omnaas

Publications

1.2K

Citations

H-Index

Concepts

All Affiliations

University of Michigan Institute of Medicinal Plant Development University of Arizona Oak Ridge National Laboratory University of Tennessee at Knoxville

About

John R. Omnaas is an author at University of Michigan specializing in medicine, biochemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	498
2	Natural Sciences	9	9	339
3	Engineering	1	1	14
4	Health Sciences	1	1	166
5	Anesthesia	1	1	166

John R. Omnaas

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Membrane Composition Determines Pardaxin's Mechanism of Lipid Bilayer Disruption Kevin Hallock, Dong-Kuk Lee, John R. Omnaas, Biophysical Journal Proteinlipid InteractionMembrane BiophysicsBiochemistryLipid Bilayer DisruptionMembrane Biology	2002	204
Direct dependence studies in rats with agents selective for different types of opioid receptor. A. Cowan, Xing Zhu, Henry I. Mosberg, Journal of Pharmacology and Experimental Therapeutics	1988	168
Role of mu and delta receptors in the supraspinal and spinal analgesic effects of [D-Pen2, D-Pen5] enkephalin in the mouse F. Porreca, Julius S. Heyman, Henry I. Mosberg, Pain Delta ReceptorsPain MedicineMolecular PainPharmacotherapyExperimental Pharmacology	1988	166
Covalent structure of biodegradative threonine dehydratase of Escherichia coli: homology with other dehydratases. P.K. Datta, Thomas J. Goss, John R. Omnaas, Proceedings of the National Academy of Sciences Covalent StructureMolecular BiologyEscherichia ColiDsda PolypeptidesEnzymatic Modification	1987	84
Supraspinal and spinal potency of selective opioid agonists in the mouse writhing test. Frank Porreca, Henry I. Mosberg, John R. Omnaas, Journal of Pharmacology and Experimental Therapeutics	1987	76
Cyclic, disulfide- and dithioether-containing opioid tetrapeptides: Development of a ligard with high delta opioid receptor selectivity and affinity Henry I. Mosberg, John R. Omnaas, Fedor Medzihradsky, Life Sciences High DeltaBiochemistryFunctional SelectivityMedicineNatural Sciences	1988	68
Development of a Model for the .delta. Opioid Receptor Pharmacophore. 2. Conformationally Restricted Phe3 Replacements in the Cyclic .delta. Receptor Selective Tetrapeptide Tyr-c[D-Cys-Phe-D-Pen]OH (JOM-13) Henry I. Mosberg, John R. Omnaas, Andrei L. Lomize, Journal of Medicinal Chemistry Drug TargetAltmetric Attention ScorePharmacotherapyPeg DavisChemical Biology	1994	56
Role of mu and delta receptors in the supraspinal and spinal analgesic effects of [D-Pen2, D-Pen5]enkephalin in the mouse. F. Porreca, Julius S. Heyman, Henry I. Mosberg, Journal of Pharmacology and Experimental Therapeutics	1987	44
Structural requirements for delta opioid receptor binding. Henry I. Mosberg, John R. Omnaas, A Goldstein Molecular Pharmacology	1987	39
Dithioether-containing cyclic peptides Henry I. Mosberg, John R. Omnaas Journal of the American Chemical Society Peptide EngineeringDatabasesAltmetric Attention ScoreBibliometricsOrganic Chemistry	1985	34

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