PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 32504068-3 2020 We demonstrate that beta-sitosterol (150-450 mug/mL) dose-dependently suppresses inflammatory response through NF-kappaB and p38 mitogen-activated protein kinase (MAPK) signaling in influenza A virus (IAV)-infected cells, which was accompanied by decreased induction of interferons (IFNs) (including Type I and III IFN). gamma-sitosterol 20-35 nuclear factor kappa B subunit 1 Homo sapiens 111-120 32308701-0 2020 beta-Sitosterol Protects against Myocardial Ischemia/Reperfusion Injury via Targeting PPARgamma/NF-kappaB Signalling. gamma-sitosterol 0-15 nuclear factor kappa B subunit 1 Homo sapiens 96-105 32308701-5 2020 Moreover, beta-sitosterol treatment counteracted the inhibitory effects of H/R treatment on the peroxisome proliferator-activated receptor gamma (PPARgamma) expression and enhanced effects of H/R treatment on the NF-kappaB expression in cardiomyocytes. gamma-sitosterol 10-25 nuclear factor kappa B subunit 1 Homo sapiens 213-222 32308701-9 2020 The beta-sitosterol-mediated cardioprotective effects may involve the modulation of PPARgamma/NF-kappaB signalling during myocardial I/R injury. gamma-sitosterol 4-19 nuclear factor kappa B subunit 1 Homo sapiens 94-103 20558233-9 2010 To elucidate the molecular mechanism of inhibition of cell adhesion molecules, we investigated the status of nuclear transcription factor-kappaB (NF-kappaB) and were able to establish that beta-sitosterol significantly blocked the TNFalpha-induced activation of NF-kappaB. gamma-sitosterol 189-204 nuclear factor kappa B subunit 1 Homo sapiens 109-144 20558233-9 2010 To elucidate the molecular mechanism of inhibition of cell adhesion molecules, we investigated the status of nuclear transcription factor-kappaB (NF-kappaB) and were able to establish that beta-sitosterol significantly blocked the TNFalpha-induced activation of NF-kappaB. gamma-sitosterol 189-204 nuclear factor kappa B subunit 1 Homo sapiens 146-155 20558233-9 2010 To elucidate the molecular mechanism of inhibition of cell adhesion molecules, we investigated the status of nuclear transcription factor-kappaB (NF-kappaB) and were able to establish that beta-sitosterol significantly blocked the TNFalpha-induced activation of NF-kappaB. gamma-sitosterol 189-204 nuclear factor kappa B subunit 1 Homo sapiens 262-271