Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Dilsah Ezgi Yilmaz"'
Autor:
Beyza Ozgen, Sefika Pinar Senol, Dilsah Ezgi Yilmaz, Meryem Temiz-Resitoglu, Omer Bahceli, Bahar Tunctan
Publikováno v:
Pharmacia, Vol 70, Iss 4, Pp 1345-1354 (2023)
Objectives: This study aimed to investigate the effect of the gasdermin D (GSDMD) and mixed lineage kinase domain-like pseudokinase (MLKL) inhibitor, necrosulfonamide (NSA), on lipopolysaccharide (LPS)-induced hyperalgesia in mice. Methods: Reaction
Externí odkaz:
https://doaj.org/article/d3682546f2bc4a95a1924a6cfab0b36d
Autor:
Beyza Ozgen, Sefika Pinar Senol, Dilsah Ezgi Yilmaz, Meryem Temiz-Resitoglu, Omer Bahceli, Bahar Tunctan
Recent studies have demonstrated that two distinct forms of necrotic cell death, pyroptosis, and necroptosis, triggered by the lipid A part of lipopolysaccharide (LPS) are involved in the pathogenesis of several neurodegenerative diseases associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3a288769e52451f4c3e0ee29b3200f12
https://doi.org/10.21203/rs.3.rs-1727695/v1
https://doi.org/10.21203/rs.3.rs-1727695/v1
Autor:
Dilsah Ezgi Yilmaz, Sefika Pinar Senol, Meryem Temiz-Resitoglu, Seyhan Sahan-Firat, Bahar Tunctan
Objective The nucleotide-binding oligomerization domain-like receptor X1 (NLRX1) has been associated with various anti-inflammatory mechanisms. We investigated whether the NLRX1 ligand docosahexaenoic acid (DHA) ameliorates lipopolysaccharide (LPS)-i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b603a9ed81187d766293db6fa66ad27d
https://doi.org/10.21203/rs.3.rs-1403191/v1
https://doi.org/10.21203/rs.3.rs-1403191/v1
Autor:
Bahar Tunctan, Sefika Pinar Senol, Meryem Temiz-Resitoglu, Dilsah Ezgi Yilmaz, Demet Sinem Guden, Omer Bahceli, Mehmet Furkan Horat, Seyhan Sahan-Firat, Ayse Nihal Sari, John R. Falck, Raghunath Reddy Anugu, Kafait U. Malik
Publikováno v:
Journal of cardiovascular pharmacology. 80(2)
The orphan receptor, G protein-coupled receptor (GPR) 75, which has been shown to mediate various effects of 20-hydroxyeicosatetraenoic acid (20-HETE), is considered as a therapeutic target in the treatment of cardiovascular diseases in which changes