Brigham and Women's Hospital
United States
John A. Badwey spends much of his time researching Biochemistry, Superoxide, Protein kinase A, Protein kinase C and Cell biology. His study in the field of Superoxide release is also linked to topics like Text mining. His Superoxide research is multidisciplinary, incorporating perspectives in Polyunsaturated fatty acid, Arachidonic acid, Lipid signaling and Hydrogen peroxide.
In the field of Protein kinase A, his study on Akt/PKB signaling pathway overlaps with subjects such as Vascular smooth muscle contraction. His MAP2K7 research extends to the thematically linked field of Protein kinase C. When carried out as part of a general Cell biology research project, his work on NADPH oxidase complex, Phosphorylation, NADPH oxidase and Wortmannin is frequently linked to work in MAPK1, therefore connecting diverse disciplines of study.
His primary areas of study are Biochemistry, Superoxide, Cell biology, Kinase and Phosphorylation. His study in Protein kinase C, Protein kinase A, Mitogen-activated protein kinase kinase, MAP2K7 and c-Raf is carried out as part of his studies in Biochemistry. His work deals with themes such as Phagocytosis, Oxidase test, Phorbol and Stimulation, which intersect with Superoxide.
His biological study spans a wide range of topics, including Receptor and Cofilin. John A. Badwey combines subjects such as Molecular biology and Chemotaxis with his study of Kinase. His studies in Phosphorylation integrate themes in fields like Proinflammatory cytokine and Peptide.
The scientist’s investigation covers issues in Cell biology, Phosphorylation, Kinase, Biochemistry and Molecular biology. His Cell biology research includes themes of Calmodulin and Cofilin, Actin cytoskeleton. His study in Phosphorylation is interdisciplinary in nature, drawing from both Receptor and Chemotaxis.
His biological study deals with issues like Signal transduction, which deal with fields such as Proinflammatory cytokine. Many of his studies on Biochemistry apply to Stereochemistry as well. His study looks at the relationship between Molecular biology and fields such as Diacylglycerol kinase, as well as how they intersect with chemical problems.
His primary areas of study are Molecular biology, Phosphorylation, Cell biology, Chemotaxis and Inflammation. John A. Badwey focuses mostly in the field of Molecular biology, narrowing it down to matters related to Kinase and, in some cases, Intracellular. Superoxide is closely connected to Signal transduction in his research, which is encompassed under the umbrella topic of Chemotaxis.
His study with Superoxide involves better knowledge in Biochemistry. His work in Inflammation tackles topics such as Periodontitis which are related to areas like Protein kinase C. His Phosphatase research incorporates themes from Staurosporine, Calmodulin, Cofilin and Phospholipase C.
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.
Active Oxygen Species and the Functions of Phagocytic Leukocytes
John A. Badwey;Manfred L. Karnovsky.
Annual Review of Biochemistry (1980)
Effects of free fatty acids on release of superoxide and on change of shape by human neutrophils. Reversibility by albumin.
J A Badwey;J T Curnutte;J M Robinson;C B Berde.
Journal of Biological Chemistry (1984)
cis-Polyunsaturated fatty acids induce high levels of superoxide production by human neutrophils.
J A Badwey;J T Curnutte;M L Karnovsky.
Journal of Biological Chemistry (1981)
Enhanced superoxide release and elevated protein kinase C activity in neutrophils from diabetic patients: association with periodontitis
M. Karima;A. Kantarci;T. Ohira;H. Hasturk.
Journal of Leukocyte Biology (2005)
Studies on the mechanism of superoxide release from human neutrophils stimulated with arachidonate.
J T Curnutte;J A Badwey;J M Robinson;M J Karnovsky.
Journal of Biological Chemistry (1984)
Superoxide release by neutrophils: Synergistic effects of a phorbol ester and a calcium ionophore
John M. Robinson;John A. Badwey;Manfred L. Karnovsky;Morris J. Karnovsky.
Biochemical and Biophysical Research Communications (1984)
Antagonists of phosphatidylinositol 3-kinase block activation of several novel protein kinases in neutrophils
Jiabing Ding;C. J. Vlahos;Ruichun Liu;R. F. Brown.
Journal of Biological Chemistry (1995)
The NADPH oxidase complex of phagocytic leukocytes: a biochemical and cytochemical view.
John M. Robinson;John A. Badwey.
Histochemistry and Cell Biology (1995)
A Molecular Defect in Intracellular Lipid Signaling in Human Neutrophils in Localized Aggressive Periodontal Tissue Damage
Karsten Gronert;Alpdogan Kantarci;Bruce D. Levy;Clary B. Clish.
Journal of Immunology (2004)
Protein phosphorylation associated with the stimulation of neutrophils. Modulation of superoxide production by protein kinase C and calcium
Paul G. Heyworth;John A. Badwey;John A. Badwey.
Journal of Bioenergetics and Biomembranes (1990)
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:
Harvard University
Scripps Research Institute
Harvard University
Harvard University
Boston Children's Hospital
Beth Israel Deaconess Medical Center
Boston University
Brigham and Women's Hospital
University of Padua
Broad Institute
Peking University
Harvard University
University of Toronto
Kyoto University
Université Laval
University of Cambridge
Bedford Institute of Oceanography
Catalan Institute for Water Research
Federal University of Rio Grande do Norte
Stony Brook University
University of Adelaide
Ludwig-Maximilians-Universität München
University of Quebec at Montreal
University of Minnesota
Brown University
University of Sydney