What is she best known for?
The fields of study she is best known for:
Julie K. Andersen mainly focuses on Substantia nigra, Oxidative stress, Parkinson's disease, Dopaminergic and Neurodegeneration.
Julie K. Andersen interconnects Neurotoxicity and MPTP in the investigation of issues within Substantia nigra.
Her Oxidative stress study integrates concerns from other disciplines, such as Mitochondrion and Cell biology.
As part of her studies on Parkinson's disease, Julie K. Andersen often connects relevant subjects like Neuroscience.
Her Dopaminergic study is concerned with the field of Dopamine as a whole.
Julie K. Andersen combines subjects such as Glutathione and Protein degradation with her study of Endocrinology.
Her most cited work include:
- Oxidative stress in neurodegeneration: cause or consequence? (1373 citations)
- Mice Deficient in Cellular Glutathione Peroxidase Show Increased Vulnerability to Malonate, 3-Nitropropionic Acid, and 1-Methyl-4-Phenyl-1,2,5,6-Tetrahydropyridine (1050 citations)
- Genetic or Pharmacological Iron Chelation Prevents MPTP-Induced Neurotoxicity In Vivo: A Novel Therapy for Parkinson's Disease (512 citations)
What are the main themes of her work throughout her whole career to date?
Her scientific interests lie mostly in Oxidative stress, Parkinson's disease, Cell biology, Substantia nigra and Dopaminergic.
Her Oxidative stress study combines topics in areas such as Alzheimer's disease and Molecular biology.
Her Parkinson's disease study incorporates themes from Paraquat, Neurodegeneration and Pharmacology.
Her research in Cell biology intersects with topics in Calcium, Apoptosis, Programmed cell death and Caenorhabditis elegans.
The concepts of her Substantia nigra study are interwoven with issues in Ferritin, Mitochondrion, MPTP and Neuroprotection.
Her Dopaminergic study deals with Glutathione intersecting with Cysteine, Antioxidant and Protein degradation.
She most often published in these fields:
- Oxidative stress (37.79%)
- Parkinson's disease (34.88%)
- Cell biology (31.98%)
What were the highlights of her more recent work (between 2013-2021)?
- Cell biology (31.98%)
- Parkinson's disease (34.88%)
- Pharmacology (16.86%)
In recent papers she was focusing on the following fields of study:
Julie K. Andersen mainly investigates Cell biology, Parkinson's disease, Pharmacology, Neurodegeneration and Neuroscience.
Her studies in Cell biology integrate themes in fields like Autophagy, Regulator, Neurotoxin and Caenorhabditis elegans.
She studies Parkinson's disease, namely Substantia nigra.
Her Substantia nigra study is associated with Dopaminergic.
Julie K. Andersen has included themes like Glycogen synthase and MPTP in her Pharmacology study.
Her Neuroscience research is multidisciplinary, incorporating elements of Parkin and Disease.
Between 2013 and 2021, her most popular works were:
- Cellular Senescence Is Induced by the Environmental Neurotoxin Paraquat and Contributes to Neuropathology Linked to Parkinson's Disease (146 citations)
- Cellular senescence and the aging brain. (135 citations)
- Mitochondrial Quality Control via the PGC1α-TFEB Signaling Pathway Is Compromised by Parkin Q311X Mutation But Independently Restored by Rapamycin (66 citations)
In her most recent research, the most cited papers focused on:
The scientist’s investigation covers issues in Cell biology, Neuroprotection, Substantia nigra, Pharmacology and Neurodegeneration.
Her Cell biology study combines topics from a wide range of disciplines, such as Regulator, Biochemistry and Caenorhabditis elegans.
Her study looks at the relationship between Neuroprotection and topics such as MPTP, which overlap with Agonist, Dopaminergic Cell, Downregulation and upregulation and Pars compacta.
Her Substantia nigra study is concerned with the larger field of Dopaminergic.
As a part of the same scientific study, Julie K. Andersen usually deals with the Dopaminergic, concentrating on Parkinson's disease and frequently concerns with Lithium, Genetically modified mouse and Neuroscience.
Her Pharmacology research is multidisciplinary, incorporating perspectives in Oxidative stress and Neurotoxicity.
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