Search Results - "FGF1"

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  1. 1

    Scaffolds for liver tissue engineering: in vitro co-culture & in vivo release by Hammond, John Stotesbury

    Published 2009
    “…Hepatocyte growth factor (HGF), epidermal growth factor (EGF), fibroblast growth factor (FGF)1, FGF2 and liver derived ECM (L-ECM) are then loaded into poly(lactic-co-glycolic acid) (PLGA) + 5% poly(ethylene glycol) (PEG) scaffolds and implanted into normal and partially hepatectomised liver. …”
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  2. 2

    A 1, 4-benzoquinone derivative isolated from Ardisia crispa (Thunb.) A. DC. root suppresses angiogenesis via its angiogenic signaling cascades by Lim, Wen Jun, Chan, Pit Foong, Hamid, Roslida Abd

    Published 2024
    “…Additionally, AC2 significantly attenuated most of the analyzed protein markers, including pro-MMP-2, VEGF-C, VEGF-D, angiopoietin-2, endothelin-1, fibroblast growth factor (FGF)-1, FGF-2, follistatin, heparin-binding epidermal growth factor-like growth factor (HB-EGF), and hepatocyte growth factor (HGF) at all tested concentrations. …”
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  3. 3

    Investigating the effects of testosterone on uterine fluid regulation and endometrial receptivity in a rat model / Mohd Helmy Mokhtar by Mohd Helmy , Mokhtar

    Published 2016
    “…Meanwhile, in the intact rats, testosterone administration from day 1 to day 3 of pregnancy suppressed pinopodes development, reduced the complexity of endometrial tight junctions and expressions of MECA-79, claudin-4, occludin, αvβ3 integrin, E-cadherin, Muc-1, Msx-1, Fgf-1 and Ihh proteins. Testosterone also reduced the number of embryo implantation. …”
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  4. 4

    Anti-metastatic and anti-angiogenic effects of curcumin analog DK1 on human osteosarcoma cells in vitro by Aziz, Muhammad Nazirul Mubin, Che Rahim, Nurul Fattin, Hussin, Yazmin, Yeap, Swee Keong, Masarudin, Mas Jaffri, Mohamad, Nurul Elyani, Akhtar, Muhammad Nadeem, Osman, Mohd Azuraidi, Cheah, Yoke Kqueen, Alitheen, Noorjahan Banu

    Published 2021
    “…Finally, DK1 also has successfully hindered the metastatic and angiogenic capability of OS cell lines by down-regulating the expression of pro-metastatic genes and proteins like MMP3, COL11A1, FGF1, Endoglin, uPA, and IGFBP2 in U-2 OS. Whilst for MG-63, the significantly down-regulated oncogenes were Serpin E1, AKT2, VEGF, uPA, PD-ECGF, and Endoglin. …”
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