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Journal Abstract Search

72 related items for PubMed ID: 18974773

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  • 2. Reversine induces multipotency of lineage-committed cells through epigenetic silencing of miR-133a.
    Kim M, Yi SA, Lee H, Bang SY, Park EK, Lee MG, Nam KH, Yoo JH, Lee DH, Ryu HW, Kwon SH, Han JW.
    Biochem Biophys Res Commun; 2014 Feb 28; 445(1):255-62. PubMed ID: 24513286
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  • 3. Trivalent dimethylarsenic compound induces histone H3 phosphorylation and abnormal localization of Aurora B kinase in HepG2 cells.
    Suzuki T, Miyazaki K, Kita K, Ochi T.
    Toxicol Appl Pharmacol; 2009 Dec 15; 241(3):275-82. PubMed ID: 19716834
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  • 4. Reversine, a novel Aurora kinases inhibitor, inhibits colony formation of human acute myeloid leukemia cells.
    D'Alise AM, Amabile G, Iovino M, Di Giorgio FP, Bartiromo M, Sessa F, Villa F, Musacchio A, Cortese R.
    Mol Cancer Ther; 2008 May 15; 7(5):1140-9. PubMed ID: 18483302
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  • 5. Aurora B couples chromosome alignment with anaphase by targeting BubR1, Mad2, and Cenp-E to kinetochores.
    Ditchfield C, Johnson VL, Tighe A, Ellston R, Haworth C, Johnson T, Mortlock A, Keen N, Taylor SS.
    J Cell Biol; 2003 Apr 28; 161(2):267-80. PubMed ID: 12719470
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  • 6. Validating Aurora B as an anti-cancer drug target.
    Girdler F, Gascoigne KE, Eyers PA, Hartmuth S, Crafter C, Foote KM, Keen NJ, Taylor SS.
    J Cell Sci; 2006 Sep 01; 119(Pt 17):3664-75. PubMed ID: 16912073
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  • 8. Overexpression of an Aurora-C kinase-deficient mutant disrupts the Aurora-B/INCENP complex and induces polyploidy.
    Chen HL, Tang CJ, Chen CY, Tang TK.
    J Biomed Sci; 2005 Sep 01; 12(2):297-310. PubMed ID: 15917996
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  • 9. Histone H3 serine 10 phosphorylation by Aurora B causes HP1 dissociation from heterochromatin.
    Hirota T, Lipp JJ, Toh BH, Peters JM.
    Nature; 2005 Dec 22; 438(7071):1176-80. PubMed ID: 16222244
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  • 12. Reversine increases the plasticity of lineage-committed mammalian cells.
    Chen S, Takanashi S, Zhang Q, Xiong W, Zhu S, Peters EC, Ding S, Schultz PG.
    Proc Natl Acad Sci U S A; 2007 Jun 19; 104(25):10482-7. PubMed ID: 17566101
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  • 13. Differentiation of C2C12 myoblasts expressing lamin A mutated at a site responsible for Emery-Dreifuss muscular dystrophy is improved by inhibition of the MEK-ERK pathway and stimulation of the PI3-kinase pathway.
    Favreau C, Delbarre E, Courvalin JC, Buendia B.
    Exp Cell Res; 2008 Apr 01; 314(6):1392-405. PubMed ID: 18294630
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  • 14. ASAP is a novel substrate of the oncogenic mitotic kinase Aurora-A: phosphorylation on Ser625 is essential to spindle formation and mitosis.
    Venoux M, Basbous J, Berthenet C, Prigent C, Fernandez A, Lamb NJ, Rouquier S.
    Hum Mol Genet; 2008 Jan 15; 17(2):215-24. PubMed ID: 17925329
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  • 15. The dietary flavonoid luteolin inhibits Aurora B kinase activity and blocks proliferation of cancer cells.
    Xie F, Lang Q, Zhou M, Zhang H, Zhang Z, Zhang Y, Wan B, Huang Q, Yu L.
    Eur J Pharm Sci; 2012 Aug 15; 46(5):388-96. PubMed ID: 22449725
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  • 16. Induction of growth arrest and polycomb gene expression by reversine allows C2C12 cells to be reprogrammed to various differentiated cell types.
    Shan SW, Tang MK, Chow PH, Maroto M, Cai DQ, Lee KK.
    Proteomics; 2007 Dec 15; 7(23):4303-16. PubMed ID: 17973295
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