1998 - Fellow of the American Association for the Advancement of Science (AAAS)
1996 - Fellow of the American Academy of Arts and Sciences
1994 - Member of the National Academy of Medicine (NAM)
Member of the Association of American Physicians
His primary areas of investigation include Internal medicine, Endocrinology, Prostaglandin, Arachidonic acid and Metabolite. His Internal medicine study frequently draws connections between adjacent fields such as Cardiology. In his study, Prostacyclin, Leukotriene E4, Endogeny and Eicosanoid is strongly linked to Ex vivo, which falls under the umbrella field of Endocrinology.
His research on Prostaglandin also deals with topics like
His primary scientific interests are in Internal medicine, Endocrinology, Biochemistry, Pharmacology and Prostaglandin. His work deals with themes such as Cyclooxygenase and Cardiology, which intersect with Internal medicine. All of his Endocrinology and Excretion, Renin–angiotensin system, Prostacyclin, Metabolism and Lipid peroxidation investigations are sub-components of the entire Endocrinology study.
The Pharmacology study combines topics in areas such as Guanethidine and In vivo. His Prostaglandin research incorporates themes from Prostaglandin E2 and Prostaglandin E. His Metabolite study incorporates themes from Urine and Chromatography.
Internal medicine, Biochemistry, Endocrinology, Cyclooxygenase and Lipid peroxidation are his primary areas of study. His work carried out in the field of Internal medicine brings together such families of science as Gastroenterology and Cardiology. As part of his studies on Biochemistry, John A. Oates frequently links adjacent subjects like In vivo.
His Endocrinology research is multidisciplinary, incorporating elements of Apolipoprotein E, Thromboxane B2 and Macrophage polarization. John A. Oates combines subjects such as Arachidonic acid, Prostaglandin and Pharmacology with his study of Cyclooxygenase. John A. Oates has researched Lipid peroxidation in several fields, including Malondialdehyde, Familial hypercholesterolemia, Cholesterol and Function.
His primary areas of study are Cyclooxygenase, Biochemistry, Internal medicine, Arachidonic acid and Endocrinology. The various areas that he examines in his Cyclooxygenase study include Platelet activation, Aspirin and Pharmacology. His work on Lipid peroxidation, Prostaglandin and Heme is typically connected to Dorsal root ganglion as part of general Biochemistry study, connecting several disciplines of science.
His Internal medicine research integrates issues from Gastroenterology, Pediatrics and Cardiology. His Arachidonic acid research is multidisciplinary, incorporating perspectives in Endocannabinoid system, Oxygenation, Ibuprofen, Flurbiprofen and Enantiomer. His Endocrinology research includes elements of Apolipoprotein E and Macrophage.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
2009 Focused Update Incorporated Into the ACC/AHA 2005 Guidelines for the Diagnosis and Management of Heart Failure in Adults A Report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines: Developed in Collaboration With the International Society for Heart and Lung Transplantation
Sharon Ann Hunt;William T. Abraham;Marshall H. Chin;Arthur M. Feldman.
Circulation (2009)
Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework*
Arthur J. Atkinson;Wayne A. Colburn;Victor G. DeGruttola;David L. DeMets.
Clinical Pharmacology & Therapeutics (2001)
ACC/AHA 2005 Guideline Update for the Diagnosis and Management of Chronic Heart Failure in the Adult
Sharon Ann Hunt;William T. Abraham;Marshall H. Chin.
Circulation (2005)
Increase in circulating products of lipid peroxidation (F2-isoprostanes) in smokers. Smoking as a cause of oxidative damage.
Jason D. Morrow;Balz Frei;Atkinson W. Longmire;J. Michael Gaziano.
The New England Journal of Medicine (1995)
Effects of caffeine on plasma renin activity, catecholamines and blood pressure.
D Robertson;J C Frölich;R K Carr;J T Watson.
The New England Journal of Medicine (1978)
Prostaglandin D2 generation after activation of rat and human mast cells with anti-IgE.
R A Lewis;N A Soter;P T Diamond;K F Austen.
Journal of Immunology (1982)
Endogenous biosynthesis of prostacyclin and thromboxane and platelet function during chronic administration of aspirin in man.
G A FitzGerald;J A Oates;J Hawiger;R L Maas.
Journal of Clinical Investigation (1983)
Plasma propranolol levels in adults with observations in four children.
D. G. Shand;E. M. Nuckolls;J. A. Oates.
Clinical Pharmacology & Therapeutics (1970)
Coronary arterial smooth muscle contraction by a substance released from platelets: evidence that it is thromboxane A2.
EF Ellis;O Oelz;LJ Roberts;NA Payne.
Science (1976)
Urinary prostaglandins. Identification and origin.
J C Frölich;T W Wilson;B J Sweetman;M Smigel.
Journal of Clinical Investigation (1975)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Vanderbilt University
Vanderbilt University
Vanderbilt University Medical Center
Vanderbilt University
University of Glasgow
Vanderbilt University
University of Pennsylvania
National Institutes of Health
Vanderbilt University
University of Pittsburgh
Eindhoven University of Technology
Complutense University of Madrid
Georgia Institute of Technology
Princeton University
University of Nottingham Ningbo China
Advanced Micro Devices (United States)
South China University of Technology
ExxonMobil (United States)
Cincinnati Children's Hospital Medical Center
J. Craig Venter Institute
University of Illinois at Urbana-Champaign
University of Pennsylvania
Uppsala University
Université Catholique de Louvain
University of Southern California
University of La Laguna