|1.||Eun, Su-Hyeon: 2 articles (09/2015 - 08/2015)|
|2.||Lee, Sang-Yun: 2 articles (09/2015 - 08/2015)|
|3.||Nguyen, Minh Duc: 2 articles (09/2015 - 08/2015)|
|4.||Kim, Dong-Hyun: 2 articles (09/2015 - 08/2015)|
|5.||Park, Jeong Hill: 2 articles (09/2015 - 08/2015)|
|6.||Jeong, Jin-Ju: 2 articles (09/2015 - 08/2015)|
|7.||Van Le, Thi Hong: 1 article (09/2015)|
|8.||Le, Thi Hong Van: 1 article (08/2015)|
|9.||Wang, Hongbo: 1 article (01/2013)|
|10.||Tian, Jingwei: 1 article (01/2013)|
08/12/2015 - "These findings suggest that orally administered MR2 may be metabolized to ocotillol in the intestine by gut microbiota and the transformed ocotillol may ameliorate inflammatory diseases such as colitis by restoring the balance of Th17/Treg cells. "
08/12/2015 - "We also examined the anti-inflammatory effect of ocotillol in mice with 2,4,6-trinitrobenzenesulfonic acid (TNBS)-induced colitis. "
08/12/2015 - "Ocotillol, a Majonoside R2 Metabolite, Ameliorates 2,4,6-Trinitrobenzenesulfonic Acid-Induced Colitis in Mice by Restoring the Balance of Th17/Treg Cells."
01/01/2013 - "Our results showed ocotillol to enhance Dox-induced cell death in p53 wild-type cancer cells. "
01/01/2013 - "Furthermore, ocotillol significantly increased the antitumor activity of Dox in A549 xenograft tumor in nude mice. "
01/01/2013 - "MTT assays and xenograft tumor model were firstly conducted to evaluate the effect of ocotillol on the antitumor activity of Dox. "
09/01/2015 - "vietnamensis may be metabolized to ocotillol via PRT4, and the metabolites, particularly ocotillol, may inhibit inflammation by inhibiting the binding of LPS to TLR4 on macrophages."
09/01/2015 - "Among the tested ginsenosides, ocotillol exhibited the strongest inhibitory effect on inflammation in LPS-stimulated macrophages via the NF-κB signaling pathway. "
|1.||Heterologous Transplantation (Xenotransplantation)