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mpc  (Mesoblast Ltd)

 
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    Mesoblast Ltd mpc
    Mpc, supplied by Mesoblast Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mpc/mpc/pmc13176351-36-4-5
    Average 86 stars, based on 1 article reviews
    mpc - by Bioz Stars, 2026-10
    86/100 stars

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    Related Articles

    other:

    Article Title: Clinical translational research on stem cell products: prospects and challenges
    Article Snippet: Mesenchymal precursor cells , MPC (Mesoblast Ltd) , Bone repair , Australia , 2010.

    Produced:

    Article Title: Transplantation of Hepatocyte Growth Factor-Modified Dental Pulp Stem Cells Prevents Bone Loss in the Early Phase of Ovariectomy-Induced Osteoporosis.
    Article Snippet: Th is pa pe r h as b ee n pe er ‐re vie we d an d ac ce pt ed fo r p ub lic at io n, b ut h as ye t t o un de rg o co py ed iti ng an d pr oo f c or re ct io n. Th e f in al pu bl ish ed ve rs io n m ay d iff er fr om th is pr oo f. Transplantation of HGF modified Dental Pulp Stem Cells Prevents Bone Loss in the Early Phase of Ovariectomy‐induced Osteoporosis Fanxuan Kong,1,2,4 Xuefeng Shi,1,3 Fengjun Xiao, 1,2,4 Yuefeng Yang, 1,2,4 Xiaoyan Zhang,1,2 Li‐ Sheng Wang, 1,2,4 Chu‐Tse Wu, 1,2,4# Hua Wang, 1,2, 4#



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    Image Search Results


    Concomitant treatment with ruxolitinib protects VSV-IFNβ-NIS treated MPC-11 tumor-bearing Balb/c mice from toxicity (A) Kaplan-Meier survival, (B) individual tumor volumes, (C) predicted tumor volumes using mixed effects modeling, (D) plasma IFNβ, (E) ALT, (F) AST, and (G) platelet count of mice at scheduled bleeds on day 3 and day 14, or at necropsy (at various time points). Treatment groups are color coded, saline (black, n = 5), VSV alone (red, n = 10), ruxolitinib (gray, n = 5), and VSV plus ruxolitinib (blue, n = 10). One intravenous dose of VSV at 10 7 TCID 50 was given per mouse, and/or ruxolitinib at 2 mg twice a day by oral gavage for 10 days, starting on the same day as VSV therapy.

    Journal: Molecular Therapy Oncology

    Article Title: Endothelial injury is a central driver of systemic IFN-β toxicity and is reversible through Jak inhibition

    doi: 10.1016/j.omton.2026.201226

    Figure Lengend Snippet: Concomitant treatment with ruxolitinib protects VSV-IFNβ-NIS treated MPC-11 tumor-bearing Balb/c mice from toxicity (A) Kaplan-Meier survival, (B) individual tumor volumes, (C) predicted tumor volumes using mixed effects modeling, (D) plasma IFNβ, (E) ALT, (F) AST, and (G) platelet count of mice at scheduled bleeds on day 3 and day 14, or at necropsy (at various time points). Treatment groups are color coded, saline (black, n = 5), VSV alone (red, n = 10), ruxolitinib (gray, n = 5), and VSV plus ruxolitinib (blue, n = 10). One intravenous dose of VSV at 10 7 TCID 50 was given per mouse, and/or ruxolitinib at 2 mg twice a day by oral gavage for 10 days, starting on the same day as VSV therapy.

    Article Snippet: MPC-11 murine plasmacytoma cells (CCL-167, American Type Culture Collection, Manassas, VA) were maintained in DMEM supplemented with 10% fetal bovine serum.

    Techniques: Clinical Proteomics, Saline