What is she best known for?
The fields of study she is best known for:
- Gene
- Mitochondrion
- Apoptosis
Her scientific interests lie mostly in Mitochondrion, Cell biology, Apoptosis, Oxidative stress and Biochemistry.
Her Mitochondrion research includes themes of Cell culture, P3 peptide, Endocrinology, Internal medicine and Programmed cell death.
Her biological study spans a wide range of topics, including Autophagy, Sequestosome 1, Autophagosome, Computational biology and Physiology.
Her study focuses on the intersection of Cell biology and fields such as Molecular biology with connections in the field of SIRT3, HEK 293 cells, Transcription factor and Downregulation and upregulation.
Her studies in Apoptosis integrate themes in fields like Endoplasmic reticulum, Neurodegeneration, Amyloid beta and Neuroscience.
Her research integrates issues of Reactive oxygen species and Cytochrome c, Mitochondrial apoptosis-induced channel in her study of Oxidative stress.
Her most cited work include:
- Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (4170 citations)
- Guidelines for the use and interpretation of assays for monitoring autophagy (3242 citations)
- SIRT3 Opposes Reprogramming of Cancer Cell Metabolism through HIF1α Destabilization (536 citations)
What are the main themes of her work throughout her whole career to date?
Her main research concerns Mitochondrion, Cell biology, Autophagy, Programmed cell death and Neuroscience.
Her Mitochondrion research is multidisciplinary, relying on both Cell culture, Apoptosis and Neurodegeneration, Parkinson's disease, Disease.
The Cell biology study which covers Mitochondrial DNA that intersects with Endogeny.
Her work in the fields of Autophagy, such as Cellular homeostasis and Autophagosome, intersects with other areas such as Interpretation.
Her Programmed cell death research incorporates elements of Endocrinology, TUNEL assay, Internal medicine, Chaperone-mediated autophagy and Computational biology.
Sandra M. Cardoso interconnects Inflammation and Oxidative stress in the investigation of issues within Neuroscience.
She most often published in these fields:
- Mitochondrion (51.40%)
- Cell biology (42.99%)
- Autophagy (22.43%)
What were the highlights of her more recent work (between 2018-2021)?
- Neurodegeneration (18.69%)
- Donepezil (5.61%)
- Moiety (4.67%)
In recent papers she was focusing on the following fields of study:
Her primary areas of investigation include Neurodegeneration, Donepezil, Moiety, Cell biology and Autophagy.
Sandra M. Cardoso has researched Neurodegeneration in several fields, including Neurotoxin, Tubulin, Microtubule, Tubulin binding and Innate immune system.
Her Cell biology study combines topics in areas such as Sirtuin 1, Parkinson's disease and Autophagosome maturation.
Sandra M. Cardoso usually deals with Parkinson's disease and limits it to topics linked to Protein aggregation and Mitochondrion.
Her Autophagy research is multidisciplinary, incorporating elements of Flux, Biogenesis, Computational biology and Programmed cell death.
Her study looks at the relationship between Neuroinflammation and fields such as Neuroscience, as well as how they intersect with chemical problems.
Between 2018 and 2021, her most popular works were:
- Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) (38 citations)
- Is Alzheimer's disease an inflammasomopathy? (25 citations)
- Acetylation as a major determinant to microtubule-dependent autophagy: Relevance to Alzheimer's and Parkinson disease pathology. (22 citations)
In her most recent research, the most cited papers focused on:
- Gene
- Apoptosis
- Mitochondrion
Sandra M. Cardoso mostly deals with Neurodegeneration, Autophagy, Moiety, Linker and Tacrine.
Her work carried out in the field of Neurodegeneration brings together such families of science as Tubulin, Microtubule, Tubulin binding and Flux.
Sandra M. Cardoso does research in Autophagy, focusing on Autophagosome maturation specifically.
She combines subjects such as Combinatorial chemistry, Substituent, Peptide and Benzofuran with her study of Moiety.
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