Show simple item record

dc.contributor.authorDurna Daştan, Sevgi
dc.date.accessioned2023-04-13T13:44:50Z
dc.date.available2023-04-13T13:44:50Z
dc.date.issued2022tr
dc.identifier.urihttp://dx.doi.org/10.1016/j.neuint.2022.105376
dc.identifier.urihttps://hdl.handle.net/20.500.12418/13689
dc.description.abstractNeurodegenerative disorders Parkinson’s disease is a progressive neurodegenerative disorder associated with neuroinflammatory responses that lead to the neurodegeneration of the dopaminergic neurons. These neuroinflammatory mechanisms involve various cytokines produced by the activated glial cells. Tumour Necrosis factor α (TNF α) is one of the major mediators of the neuroinflammation associated with neurodegeneration. TNF α has a dual role of neuroprotection and neurotoxicity in the brain. The effective pathways of TNF involve various signalling pathways transduced by the receptors TNFR1 and TNFR2. Effective therapeutic strategies have been produced targeting the neurotoxic behaviour of the Tumour Necrosis Factor and the associated neurodegeneration which includes the use of Dominant Negative Tumour Necrosis Factor (DN-TNF) inhibitors like XENP 345 and XPro®1595 and peroxisome proliferator receptor gamma (PPAR-γ) agonisttr
dc.language.isoengtr
dc.publisherneurochemistry internationaltr
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.neuint.2022.105376tr
dc.rightsinfo:eu-repo/semantics/openAccesstr
dc.titleThe role of Tumour Necrosis Factor in neuroinflammation associated with Parkinson's disease and targeted therapiestr
dc.typearticletr
dc.contributor.departmentFen Fakültesitr
dc.contributor.authorID0000-0003-4946-5602tr
dc.identifier.volumeocak 2022tr
dc.identifier.issue158tr
dc.identifier.endpage29tr
dc.identifier.startpage1tr
dc.relation.publicationcategoryUluslararası Editör Denetimli Dergide Makaletr


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record