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Inhibiting Nrf2 Expression Exacerbates Nlrp3 Inflammasome Activation and Dopamine Neuron Degeneration in Parkinson's Disease Models

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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/s00018-016-2223-0openalex-extracted
Role of Nrf2/HO-1 system in development, oxidative stress response and diseases: an evolutionarily conserved mechanism
inferredcites →https://doi.org/10.1007/s00109-021-02071-5openalex-extracted
Nrf2 as a potential target for Parkinson’s disease therapy
inferredcites →https://doi.org/10.1007/s00253-020-10614-yopenalex-extracted
Crosstalk between ER stress, NLRP3 inflammasome, and inflammation
inferredcites →https://doi.org/10.1007/s00281-022-00947-3openalex-extracted
The immunology of Parkinson’s disease
inferredcites →https://doi.org/10.1007/s00702-016-1563-0openalex-extracted
Nrf2: a modulator of Parkinson’s disease?
inferredcites →https://doi.org/10.1007/s12035-020-02198-5openalex-extracted
NLRP3 Inflammasome Inhibition Prevents α-Synuclein Pathology by Relieving Autophagy Dysfunction in Chronic MPTP–Treated NLRP3 Knockout Mice
inferredcites →https://doi.org/10.1007/s12264-017-0159-5openalex-extracted
Premotor Diagnosis of Parkinson’s Disease
inferredcites →https://doi.org/10.1007/s12264-023-01023-yopenalex-extracted
NLRP3 Inflammasome-Mediated Neuroinflammation and Related Mitochondrial Impairment in Parkinson’s Disease
inferredcites →https://doi.org/10.1016/j.arr.2022.101756openalex-extracted
Role of Nrf2 in aging, Alzheimer’s and other neurodegenerative diseases
inferredcites →https://doi.org/10.1016/j.intimp.2018.12.019openalex-extracted
The mechanisms of NLRP3 inflammasome/pyroptosis activation and their role in Parkinson's disease
inferredcites →https://doi.org/10.1016/j.lfs.2019.03.057openalex-extracted
Parkinson's disease: Mechanisms, translational models and management strategies
inferredcites →https://doi.org/10.1016/j.mad.2021.111512openalex-extracted
The old guard: Age-related changes in microglia and their consequences
inferredcites →https://doi.org/10.1016/j.nbd.2019.104700openalex-extracted
Autonomic dysfunction in Parkinson’s disease: Implications for pathophysiology, diagnosis, and treatment
inferredcites →https://doi.org/10.1016/j.nbd.2020.105028openalex-extracted
Microglia and astrocyte dysfunction in parkinson's disease
inferredcites →https://doi.org/10.1016/j.neuron.2022.05.009openalex-extracted
Neuronal NLRP3 is a parkin substrate that drives neurodegeneration in Parkinson’s disease
inferredcites →https://doi.org/10.1016/j.neuroscience.2020.08.004openalex-extracted
NLRP3 Inflammasomes in Parkinson’s disease and their Regulation by Parkin
inferredcites →https://doi.org/10.1016/j.pbb.2004.03.006openalex-extracted
Biochemical, behavioral and immunohistochemical alterations in MPTP-treated mouse model of Parkinson's disease
inferredcites →https://doi.org/10.1016/j.redox.2020.101696openalex-extracted
ROS systems are a new integrated network for sensing homeostasis and alarming stresses in organelle metabolic processes
inferredcites →https://doi.org/10.1016/s0140-6736(21)00218-xopenalex-extracted
Parkinson's disease
inferredcites →https://doi.org/10.1016/s0166-4328(01)00309-6openalex-extracted
Behavioral phenotyping of the MPTP mouse model of Parkinson's disease
inferredcites →https://doi.org/10.1016/s1474-4422(21)00030-2openalex-extracted
Challenges in the diagnosis of Parkinson's disease
inferredcites →https://doi.org/10.1016/s1474-4422(21)00061-2openalex-extracted
Progress towards therapies for disease modification in Parkinson's disease
inferredcites →https://doi.org/10.1038/nature09663openalex-extracted
A role for mitochondria in NLRP3 inflammasome activation
inferredcites →https://doi.org/10.1038/nprot.2006.342openalex-extracted
Protocol for the MPTP mouse model of Parkinson's disease
inferredcites →https://doi.org/10.1038/s41418-018-0124-5openalex-extracted
MPTP-driven NLRP3 inflammasome activation in microglia plays a central role in dopaminergic neurodegeneration
inferredcites →https://doi.org/10.1038/s41531-020-00147-6openalex-extracted
Plasma-borne indicators of inflammasome activity in Parkinson’s disease patients
inferredcites →https://doi.org/10.1038/s41577-019-0165-0openalex-extracted
The NLRP3 inflammasome: molecular activation and regulation to therapeutics
inferredcites →https://doi.org/10.1038/s41582-020-00435-yopenalex-extracted
Neuroinflammation and microglial activation in Alzheimer disease: where do we go from here?
inferredcites →https://doi.org/10.1080/00207454.2021.1922402openalex-extracted
NLRP3 inflammasome activation increases brain oxidative stress after transient global cerebral ischemia in rats
inferredcites →https://doi.org/10.1089/ars.2020.8065openalex-extracted
Heme-Oxygenase-1
inferredcites →https://doi.org/10.1093/brain/awab446openalex-extracted
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal state
inferredcites →https://doi.org/10.1111/acel.13522openalex-extracted
α‐synuclein suppresses microglial autophagy and promotes neurodegeneration in a mouse model of Parkinson’s disease
inferredcites →https://doi.org/10.1111/jnc.13691openalex-extracted
The clinical symptoms of Parkinson's disease
inferredcites →https://doi.org/10.1146/annurev-immunol-081022-021207openalex-extracted
Structural Mechanisms of NLRP3 Inflammasome Assembly and Activation
inferredcites →https://doi.org/10.1152/physrev.00026.2013openalex-extracted
Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release
inferredcites →https://doi.org/10.1155/2016/2183026openalex-extracted
ROS‐Mediated NLRP3 Inflammasome Activation in Brain, Heart, Kidney, and Testis Ischemia/Reperfusion Injury
inferredcites →https://doi.org/10.1186/s13041-017-0340-9openalex-extracted
Oxidative stress and cellular pathologies in Parkinson’s disease
inferredcites →https://doi.org/10.1186/s40478-021-01209-3openalex-extracted
α-Synuclein pathology in Parkinson disease activates homeostatic NRF2 anti-oxidant response
inferredcites →https://doi.org/10.2147/cia.s158513openalex-extracted
Oxidative stress, aging, and diseases
inferredcites →https://doi.org/10.3233/jpd-223237openalex-extracted
Microglia in Parkinson’s Disease
inferredcites →https://doi.org/10.3389/fphar.2022.919233openalex-extracted
Role of Nrf2 in Parkinson’s Disease: Toward New Perspectives
inferredcites →https://doi.org/10.3390/antiox11010026openalex-extracted
NRF2 Activation Ameliorates Oxidative Stress and Improves Mitochondrial Function and Synaptic Plasticity, and in A53T α-Synuclein Hippocampal Neurons
inferredcites →https://doi.org/10.3390/antiox12030731openalex-extracted
Neuroprotection of NRF2 against Ferroptosis after Traumatic Brain Injury in Mice
inferredcites →https://doi.org/10.3390/antiox9070630openalex-extracted
Antioxidant and Anti-inflammatory Effect of Nrf2 Inducer Dimethyl Fumarate in Neurodegenerative Diseases
inferredcites →https://doi.org/10.3390/cells10030515openalex-extracted
Heme Oxgenase-1, a Cardinal Modulator of Regulated Cell Death and Inflammation
inferredcites →https://doi.org/10.3390/ijms20133328openalex-extracted
The NLRP3 Inflammasome: An Overview of Mechanisms of Activation and Regulation
inferredcites →https://doi.org/10.3390/ijms21134777openalex-extracted
NRF2, a Transcription Factor for Stress Response and Beyond
inferredcites →https://doi.org/10.3390/ijms21197152openalex-extracted
Neuroprotective Effect of Antioxidants in the Brain
inferredcites →https://doi.org/10.3390/ijms23115938openalex-extracted
An Overview of Oxidative Stress, Neuroinflammation, and Neurodegenerative Diseases
inferredcites →https://doi.org/10.3390/ijms23137273openalex-extracted
Oxidative Stress in Ageing and Chronic Degenerative Pathologies: Molecular Mechanisms Involved in Counteracting Oxidative Stress and Chronic Inflammation
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