Theresa A. Kuntzweiler

Author

University of Cincinnati Medical Center

Also Known As

T A Kuntzweiler, T. A. KUNTZWEILER, T. Kuntzweiler, THERESA A. KUNTZWEILER, Theresa A. Kuntzweiler, Theresa Kuntzweiler

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

University of Cincinnati Medical Center Abbott Fund Sanofi (United States)Abbott (United Kingdom)University of Cincinnati

About

Theresa A. Kuntzweiler is an author at University of Cincinnati Medical Center specializing in biochemistry, medicine, and pharmacology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	463
2	Natural Sciences	4	4	158
3	Health Sciences	1	1	131
4	Social Sciences	1	1	39
5	Anesthesia	1	1	53

Theresa A. Kuntzweiler

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
Na+,K(+)-ATPase. Jerry B. Lingrel, Theresa A. Kuntzweiler Journal of Biological Chemistry	1994	746
Identification and Initial Structure−Activity Relationships of (<i>R</i>)-5-(2-Azetidinylmethoxy)-2-chloropyridine (ABT-594), a Potent, Orally Active, Non-Opiate Analgesic Agent Acting via Neuronal Nicotinic Acetylcholine Receptors Mark W. Holladay, James T. Wasicak, Nan‐Horng Lin, Journal of Medicinal Chemistry Pain MedicineNeuropathic PainOrally ActiveMolecular PainPharmacotherapy	1998	131
Ouabain Interactions with the H5-H6 Hairpin of the Na,K-ATPase Reveal a Possible Inhibition Mechanism via the Cation Binding Domain Maria Palasis, Theresa A. Kuntzweiler, José Argüello, Journal of Biological Chemistry	1996	109
ABT-594 [(R)-5-(2-Azetidinylmethoxy)-2-Chloropyridine]: A Novel, Orally Effective Analgesic Acting via Neuronal Nicotinic Acetylcholine Receptors: I. In Vitro Characterization Diana L. Donnelly‐Roberts, Pamela S. Puttfarcken, Theresa A. Kuntzweiler, Journal of Pharmacology and Experimental Therapeutics	1998	103
Asp804 and Asp808 in the Transmembrane Domain of the Na,K-ATPase α Subunit Are Cation Coordinating Residues Theresa A. Kuntzweiler, José Argüello, Jerry B. Lingrel Journal of Biological Chemistry	1996	99
Mono- and Disubstituted-3,8-diazabicyclo[3.2.1]octane Derivatives as Analgesics Structurally Related to Epibatidine: Synthesis, Activity, and Modeling Daniela Barlocco, Giorgio Cignarella, Donatella Tondi, Journal of Medicinal Chemistry Nmr SpectroscopyPain MedicineOrganic ChemistryPharmacotherapyHeterocycle Chemistry	1998	53
Structure-activity studies related to ABT-594, a potent nonopioid analgesic agent: Effect of pyridine and azetidine ring substitutions on nicotinic acetylcholine receptor binding affinity and analgesic activity in mice Mark W. Holladay, Hao Bai, Yihong Li, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyBiochemistryAzetidine Ring SubstitutionsPain MedicineMedicine	1998	53
Glutamic Acid 327 in the Sheep α1 Isoform of Na+,K+-ATPase Stabilizes a K+-induced Conformational Change Theresa A. Kuntzweiler, Earl T. Wallick, Carl L. Johnson, Journal of Biological Chemistry Ouabain BindingMolecular BiologyNa+ CompetitionCellular PhysiologyGlutamic Acid 327	1995	40
Synthesis and structure-activity relationships of pyridine-modified analogs of 3-[2-((S)-pyrrolidinyl)methoxy]pyridine, A-84543, a potent nicotinic acetylcholine receptor agonist Nan‐Horng Lin, David Gunn, Yihong Li, Bioorganic & Medicinal Chemistry Letters BiochemistryMedicineNicotineStructure-activity RelationshipsPharmacological Agent	1998	40
Amino Acid Replacement of Asp369 in the Sheep α1 Isoform Eliminates ATP and Phosphate Stimulation of [3]H Ouabain Binding to the Na+,K+-ATPase without Altering the Cation Binding Properties of the Enzyme Theresa A. Kuntzweiler, Earl T. Wallick, Carl L. Johnson, Journal of Biological Chemistry Ouabain BindingAmino Acid ReplacementCellular PhysiologyPhosphate StimulationCation Binding Properties	1995	40

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