John J. Lemasters spends much of his time researching Cell biology, Mitochondrion, Mitochondrial permeability transition pore, Programmed cell death and Biochemistry. His research in Cell biology intersects with topics in Membrane potential, Adenosine triphosphate and Cytosol. His Mitochondrion research incorporates themes from Autophagy, Mitochondrial Degradation, Glycolysis, Voltage-dependent anion channel and Intermembrane space.
His studies in Mitochondrial permeability transition pore integrate themes in fields like Oxidative stress, Mitochondrial membrane transport protein, Inner mitochondrial membrane, Reperfusion injury and Cyclosporin a. Programmed cell death is a subfield of Apoptosis that John J. Lemasters investigates. Within one scientific family, John J. Lemasters focuses on topics pertaining to Pharmacology under Biochemistry, and may sometimes address concerns connected to Nitric oxide synthase, Nitric oxide and Glycine.
His scientific interests lie mostly in Mitochondrion, Cell biology, Biochemistry, Mitochondrial permeability transition pore and Internal medicine. His work deals with themes such as Propidium iodide, Cytosol, Molecular biology, Depolarization and Cell killing, which intersect with Mitochondrion. His studies deal with areas such as Autophagy, Mitophagy, Voltage-dependent anion channel, Membrane potential and Programmed cell death as well as Cell biology.
John J. Lemasters interconnects Reperfusion injury, Biophysics and Pharmacology in the investigation of issues within Biochemistry. His Mitochondrial permeability transition pore research is within the category of Apoptosis. His Internal medicine study which covers Endocrinology that intersects with Fibrosis.
John J. Lemasters mainly investigates Mitochondrion, Cell biology, Biochemistry, Voltage-dependent anion channel and Mitochondrial permeability transition pore. His research integrates issues of Reactive oxygen species, Cytosol, Depolarization, Pharmacology and Mitophagy in his study of Mitochondrion. His Cell biology research is multidisciplinary, incorporating elements of Autophagy, Chemiosmosis and Programmed cell death, Propidium iodide.
His Programmed cell death study combines topics from a wide range of disciplines, such as Neuroscience and Intracellular. His Biochemistry study combines topics in areas such as Cancer cell and Biophysics. His Mitochondrial permeability transition pore study integrates concerns from other disciplines, such as Sphingosine, Myocardial infarction, Ventricular remodeling, Necrosis and Cyclosporin a.
John J. Lemasters mainly focuses on Mitochondrion, Cell biology, Biochemistry, Voltage-dependent anion channel and Autophagy. The study incorporates disciplines such as Cell killing, Pharmacology and Mitochondrial permeability transition pore in addition to Mitochondrion. His biological study spans a wide range of topics, including Chemiosmosis and Mitophagy.
His work carried out in the field of Biochemistry brings together such families of science as Molecular biology and Depolarization. His research investigates the link between Autophagy and topics such as Programmed cell death that cross with problems in Cell growth, Neurodegeneration and Physiology. His study looks at the relationship between Reactive oxygen species and fields such as Oxidative stress, as well as how they intersect with chemical problems.
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.
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Autophagy (2016)
Guidelines for the use and interpretation of assays for monitoring autophagy
Daniel J. Klionsky;Fabio C. Abdalla;Hagai Abeliovich;Robert T. Abraham.
Autophagy (2012)
Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Autophagy (2016)
Molecular mechanisms of cell death: recommendations of the Nomenclature Committee on Cell Death 2018.
Lorenzo Galluzzi;Ilio Vitale;Stuart A. Aaronson;John M. Abrams.
Cell Death & Differentiation (2018)
The mitochondrial permeability transition in cell death: a common mechanism in necrosis, apoptosis and autophagy.
John J. Lemasters;Anna Liisa Nieminen;Ting Qian;Lawrence C. Trost;Lawrence C. Trost.
Biochimica et Biophysica Acta (1998)
Selective degradation of mitochondria by mitophagy.
Insil Kim;Sara Rodriguez-Enriquez;John J. Lemasters.
Archives of Biochemistry and Biophysics (2007)
Mechanisms of Hepatotoxicity
Hartmut Jaeschke;Gregory J. Gores;Arthur I. Cederbaum;Jack A. Hinson.
Toxicological Sciences (2002)
Selective Mitochondrial Autophagy, or Mitophagy, as a Targeted Defense Against Oxidative Stress, Mitochondrial Dysfunction, and Aging
John J Lemasters.
Rejuvenation Research (2005)
Rhodamine 123 as a probe of transmembrane potential in isolated rat-liver mitochondria: spectral and metabolic properties
Ronald K. Emaus;Ron Grunwald;John J. Lemasters.
Biochimica et Biophysica Acta (1986)
Mitochondrial permeability transition: a common pathway to necrosis and apoptosis.
Jae Sung Kim;Lihua He;John J. Lemasters.
Biochemical and Biophysical Research Communications (2003)
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:
University of North Carolina at Chapel Hill
The University of Texas Health Science Center at San Antonio
University of California, San Diego
University of Kansas
National Institutes of Health
Medical University of South Carolina
Karolinska Institute
University of Rome Tor Vergata
Foundation for Research and Technology Hellas
The University of Texas Southwestern Medical Center
Technion – Israel Institute of Technology
Chalmers University of Technology
Boston College
Inha University
Spanish National Research Council
University of Colorado Boulder
University of Alabama at Birmingham
Complutense University of Madrid
University of Copenhagen
Aarhus University
Pfizer (United States)
City University of Hong Kong
Nelson Mandela University
Harvard University
Memorial Sloan Kettering Cancer Center
McGill University