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Thiol-Based Redox Molecules: Potential Antidotes for Acrylamide Toxicity
Valeria Martin
, Michael Trus
,
Daphne Atlas
*
*
Corresponding author for this work
Alexander Silberman Institute of Life Sciences
Research output
:
Contribution to journal
›
Article
›
peer-review
7
Scopus citations
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Keyphrases
Thiols
100%
Thioredoxin
100%
Acrylamide Exposure
100%
Redox Molecules
100%
Acrylamide
71%
Oxidative Stress
42%
Cysteine Residues
28%
Cysteine
28%
Parkinson's Disease
28%
Mitogen-activated Protein Kinase
28%
Mimetic Peptide
28%
L-DOPA
28%
N-acetylcysteine
28%
Cysteine-rich Peptides
28%
Cellular Level
14%
Clinical Application
14%
Potential Treatments
14%
Low Molecular Weight
14%
Stress-induced
14%
Chronic Exposure
14%
ERK2
14%
Reactive Oxygen Species
14%
TETRA
14%
Extracellular Signal-regulated Kinase
14%
Dopamine
14%
PC12 Cells
14%
P38 Mitogen-activated Protein Kinase (p38 MAPK)
14%
Induced Activation
14%
C-Jun N-terminal Kinase
14%
Kinase Activation
14%
Disulfide
14%
Textile
14%
High Efficacy
14%
Activated Protein C
14%
Reduction Property
14%
Non-aromatic
14%
N-acetylcysteine Amide
14%
Cellular Proteolysis
14%
Starchy Foods
14%
Neurotoxic Symptoms
14%
Dose-dependent
14%
Reactive Oxygen Species Scavenging
14%
Pharmacology, Toxicology and Pharmaceutical Science
Acrylamide
100%
Thiol
100%
Antidote
100%
Thioredoxin
77%
Cysteine
66%
Peptide
44%
Mitogen Activated Protein Kinase
33%
N-Acetylcysteine
33%
Reactive Oxygen Metabolite
22%
Levodopa
22%
Parkinson's Disease
22%
Long Term Exposure
11%
Carboxamide
11%
Disulfide
11%
Carbon Tetrachloride
11%
Mitogen Activated Protein Kinase 3
11%
Mitogen Activated Protein Kinase P38
11%
Cosmetic
11%
Dopamine
11%