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Ursolic Acid Reduces Inflammation in Experimental Autoimmune Encephalomyelitis by Suppressing the Tnf-Α/Nf-Κb Signaling Pathway
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inferredcites →https://doi.org/10.1002/(sici)1097-4547(19960815)45:4<322::aid-jnr1>3.0.co;2-bopenalex-extracted
Review: cytokines and the pathogenesis of multiple sclerosis
inferredcites →https://doi.org/10.1002/dneu.22455openalex-extracted
The corticospinal tract: Evolution, development, and human disorders
inferredcites →https://doi.org/10.1002/mnfr.200700389openalex-extracted
Ursolic acid: An anti‐ and pro‐inflammatory triterpenoid
inferredcites →https://doi.org/10.1007/s40263-017-0474-4openalex-extracted
Therapeutic Potential of Ursolic Acid to Manage Neurodegenerative and Psychiatric Diseases
inferredcites →https://doi.org/10.1016/j.cellimm.2018.12.003openalex-extracted
Immune response in the relapsing-remitting experimental autoimmune encephalomyelitis in mice: The role of the NF-κB signaling pathway
inferredcites →https://doi.org/10.1016/j.jneuroim.2008.04.034openalex-extracted
Expression and regulation of matrix metalloproteinase-12 in experimental autoimmune encephalomyelitis and by bone marrow derived macrophages in vitro
inferredcites →https://doi.org/10.1016/j.jphs.2020.08.002openalex-extracted
Ursolic acid treatment suppresses cuprizone-induced demyelination and motor dysfunction via upregulation of IGF-1
inferredcites →https://doi.org/10.1016/j.molmed.2013.08.001openalex-extracted
Nuclear factor kappa B (NF-κB) in multiple sclerosis pathology
inferredcites →https://doi.org/10.1016/j.nlm.2011.03.010openalex-extracted
Ursolic acid attenuates lipopolysaccharide-induced cognitive deficits in mouse brain through suppressing p38/NF-κB mediated inflammatory pathways
inferredcites →https://doi.org/10.1016/j.phrs.2005.11.005openalex-extracted
Amelioration of adjuvant-induced arthritis by ursolic acid through altered Th1/Th2 cytokine production
inferredcites →https://doi.org/10.1016/j.phymed.2020.153385openalex-extracted
Total flavonoids of astragalus attenuates experimental autoimmune encephalomyelitis by suppressing the activation and inflammatory responses of microglia via JNK/AKT/NFκB signaling pathway
inferredcites →https://doi.org/10.1016/j.taap.2018.01.023openalex-extracted
Low, but not high, dose triptolide controls neuroinflammation and improves behavioral deficits in toxic model of multiple sclerosis by dampening of NF-κB activation and acceleration of intrinsic myelin repair
inferredcites →https://doi.org/10.1016/s0165-5728(02)00024-3openalex-extracted
The expression of pro- and anti-apoptosis Bcl-2 family proteins in lymphocytes from patients with multiple sclerosis
inferredcites →https://doi.org/10.1038/nm1551openalex-extracted
A brief history of TH17, the first major revision in the TH1/TH2 hypothesis of T cell–mediated tissue damage
inferredcites →https://doi.org/10.1073/pnas.2000208117openalex-extracted
A dual effect of ursolic acid to the treatment of multiple sclerosis through both immunomodulation and direct remyelination
inferredcites →https://doi.org/10.1080/14786419.2018.1516660openalex-extracted
Anti-hypertensive effects of Radix Rehmanniae and its active ingredients
inferredcites →https://doi.org/10.1096/fj.04-2030fjeopenalex-extracted
An elevated matrix metalloproteinase (MMP) in an animal model of multiple sclerosis is protective by affecting Th1/Th2 polarization
inferredcites →https://doi.org/10.1136/jnnp-2013-307336openalex-extracted
Stimulated PBMC-produced IFN- and TNF- are associated with altered relapse risk in multiple sclerosis: results from a prospective cohort study
inferredcites →https://doi.org/10.1177/1352458509359721openalex-extracted
Suppressive effect of glucocorticoids on TNF-α production is associated with their clinical effect in multiple sclerosis
inferredcites →https://doi.org/10.1177/17562864211007687openalex-extracted
Inflammation in multiple sclerosis
inferredcites →https://doi.org/10.1182/blood-2005-04-1496openalex-extracted
Mesenchymal stem cells ameliorate experimental autoimmune encephalomyelitis inducing T-cell anergy
inferredcites →https://doi.org/10.1371/journal.pone.0031318openalex-extracted
Potent Anti-Inflammatory Activity of Ursolic Acid, a Triterpenoid Antioxidant, Is Mediated through Suppression of NF-κB, AP-1 and NF-AT
inferredcites →https://doi.org/10.2174/1871527319666200812224457openalex-extracted
Neuroprotection of Rotenone-Induced Parkinsonism by Ursolic Acid in PD Mouse Model
inferredcites →https://doi.org/10.2174/1872213x10666160711143904openalex-extracted
Ursolic Acid and Oleanolic Acid: Pentacyclic Terpenoids with Promising Anti-Inflammatory Activities
inferredcites →https://doi.org/10.22037/ijpr.2019.112181.13582openalex-extracted
Myelin Protection by Ursolic Acid in Cuprizone-Induced Demyelination in Mice.
inferredcites →https://doi.org/10.3389/fimmu.2018.00925openalex-extracted
Selective Modulation of TNF–TNFRs Signaling: Insights for Multiple Sclerosis Treatment
inferredcites →https://doi.org/10.3389/fimmu.2020.00391openalex-extracted
Nuclear Factor κB (NF-κB)–Mediated Inflammation in Multiple Sclerosis
inferredcites →https://doi.org/10.3389/fnins.2022.935166openalex-extracted
Perinatal development of central vestibular neurons in mice
inferredcites →https://doi.org/10.3389/fphar.2022.877898openalex-extracted
Ursolic Acid Protects Neurons in Temporal Lobe Epilepsy and Cognitive Impairment by Repressing Inflammation and Oxidation
inferredcites →https://doi.org/10.3390/ijms12010655openalex-extracted
Herbaceous Peony (Paeonia lactiflora Pall.) as an Alternative Source of Oleanolic and Ursolic Acids
inferredcites →https://doi.org/10.4049/jimmunol.132.5.2393openalex-extracted
The immunopathology of experimental allergic encephalomyelitis. I. Quantitative analysis of inflammatory cells in situ.
inferredcites →https://doi.org/10.4049/jimmunol.151.8.4371openalex-extracted
Cytokines and adhesion molecules contribute to the ability of myelin proteolipid protein-specific T cell clones to mediate experimental allergic encephalomyelitis.
inferredcites →https://doi.org/10.5604/01.3001.0010.3836openalex-extracted
Multiple sclerosis - etiology and diagnostic potential
inferredcites →https://doi.org/10.1016/j.sapharm.2021.06.021openalex-snapshot
An introduction to network analysis for studies of medication use
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