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Journal Abstract Search

195 related items for PubMed ID: 12145320

  • 1. Enhanced microtubule-dependent trafficking and p53 nuclear accumulation by suppression of microtubule dynamics.
    Giannakakou P, Nakano M, Nicolaou KC, O'Brate A, Yu J, Blagosklonny MV, Greber UF, Fojo T.
    Proc Natl Acad Sci U S A; 2002 Aug 06; 99(16):10855-60. PubMed ID: 12145320
    [Abstract] [Full Text] [Related]

  • 2. p53 is associated with cellular microtubules and is transported to the nucleus by dynein.
    Giannakakou P, Sackett DL, Ward Y, Webster KR, Blagosklonny MV, Fojo T.
    Nat Cell Biol; 2000 Oct 06; 2(10):709-17. PubMed ID: 11025661
    [Abstract] [Full Text] [Related]

  • 3. Kinetic stabilization of microtubule dynamic instability by benomyl increases the nuclear transport of p53.
    Rathinasamy K, Panda D.
    Biochem Pharmacol; 2008 Dec 15; 76(12):1669-80. PubMed ID: 18823952
    [Abstract] [Full Text] [Related]

  • 4. Microtubule-dependent plus- and minus end-directed motilities are competing processes for nuclear targeting of adenovirus.
    Suomalainen M, Nakano MY, Keller S, Boucke K, Stidwill RP, Greber UF.
    J Cell Biol; 1999 Feb 22; 144(4):657-72. PubMed ID: 10037788
    [Abstract] [Full Text] [Related]

  • 5. Increased p53 phosphorylation after microtubule disruption is mediated in a microtubule inhibitor- and cell-specific manner.
    Stewart ZA, Tang LJ, Pietenpol JA.
    Oncogene; 2001 Jan 04; 20(1):113-24. PubMed ID: 11244509
    [Abstract] [Full Text] [Related]

  • 6. Determination of the net exchange rate of tubulin dimer in steady-state microtubules by fluorescence correlation spectroscopy.
    Neumann T, Kirschstein SO, Camacho Gomez JA, Kittler L, Unger E.
    Biol Chem; 2001 Mar 04; 382(3):387-91. PubMed ID: 11347885
    [Abstract] [Full Text] [Related]

  • 7. [Antimicrotubule agents can activate different apoptotic pathways].
    Kisurina-Evgen'eva OP, Briantseva SA, Stil' AA, Onishchenko GE.
    Biofizika; 2006 Mar 04; 51(5):875-9. PubMed ID: 17131827
    [Abstract] [Full Text] [Related]

  • 8. The high levels of p53 present in adenovirus early region 1-transformed human cells do not cause up-regulation of MDM2 expression.
    Grand RJ, Lecane PS, Owen D, Grant ML, Roberts S, Levine AJ, Gallimore PH.
    Virology; 1995 Jul 10; 210(2):323-34. PubMed ID: 7618270
    [Abstract] [Full Text] [Related]

  • 9. Regulation of p53 by hypoxia: dissociation of transcriptional repression and apoptosis from p53-dependent transactivation.
    Koumenis C, Alarcon R, Hammond E, Sutphin P, Hoffman W, Murphy M, Derr J, Taya Y, Lowe SW, Kastan M, Giaccia A.
    Mol Cell Biol; 2001 Feb 10; 21(4):1297-310. PubMed ID: 11158315
    [Abstract] [Full Text] [Related]

  • 10. The MDM2 RING-finger domain is required to promote p53 nuclear export.
    Geyer RK, Yu ZK, Maki CG.
    Nat Cell Biol; 2000 Sep 10; 2(9):569-73. PubMed ID: 10980696
    [Abstract] [Full Text] [Related]

  • 11. Survivin regulates the p53 tumor suppressor gene family.
    Wang Z, Fukuda S, Pelus LM.
    Oncogene; 2004 Oct 21; 23(49):8146-53. PubMed ID: 15361831
    [Abstract] [Full Text] [Related]

  • 12. Like p53, the proliferation-associated protein p120 accumulates in human cancer cells following exposure to anticancer drugs.
    Blagosklonny MV, Iglesias A, Zhan Z, Fojo T.
    Biochem Biophys Res Commun; 1998 Mar 17; 244(2):368-73. PubMed ID: 9514935
    [Abstract] [Full Text] [Related]

  • 13. Nuclear exclusion of p53 in a subset of tumors requires MDM2 function.
    Lu W, Pochampally R, Chen L, Traidej M, Wang Y, Chen J.
    Oncogene; 2000 Jan 13; 19(2):232-40. PubMed ID: 10645001
    [Abstract] [Full Text] [Related]

  • 14. The microtubule cytoskeleton is required for a G2 cell cycle delay in cancer cells lacking stathmin and p53.
    Carney BK, Caruso Silva V, Cassimeris L.
    Cytoskeleton (Hoboken); 2012 May 13; 69(5):278-89. PubMed ID: 22407961
    [Abstract] [Full Text] [Related]

  • 15. P53 is transported into the nucleus via an Hsf1-dependent nuclear localization mechanism.
    Li Q, Martinez JD.
    Mol Carcinog; 2011 Feb 13; 50(2):143-52. PubMed ID: 21229611
    [Abstract] [Full Text] [Related]

  • 16. Differential regulation of mitogen-activated protein kinases by microtubule-binding agents in human breast cancer cells.
    Shtil AA, Mandlekar S, Yu R, Walter RJ, Hagen K, Tan TH, Roninson IB, Kong AN.
    Oncogene; 1999 Jan 14; 18(2):377-84. PubMed ID: 9927194
    [Abstract] [Full Text] [Related]

  • 17. Intact microtubules support adenovirus and herpes simplex virus infections.
    Mabit H, Nakano MY, Prank U, Saam B, Döhner K, Sodeik B, Greber UF.
    J Virol; 2002 Oct 14; 76(19):9962-71. PubMed ID: 12208972
    [Abstract] [Full Text] [Related]

  • 18. Regulation of transcriptional activation of mdm2 gene by p53 in response to UV radiation.
    Saucedo LJ, Carstens BP, Seavey SE, Albee LD, Perry ME.
    Cell Growth Differ; 1998 Feb 14; 9(2):119-30. PubMed ID: 9486848
    [Abstract] [Full Text] [Related]

  • 19. A transforming p53 mutant, which binds DNA, transactivates and induces apoptosis reveals a nuclear:cytoplasmic shuttling defect.
    Crook T, Parker GA, Rozycka M, Crossland S, Allday MJ.
    Oncogene; 1998 Mar 14; 16(11):1429-41. PubMed ID: 9525742
    [Abstract] [Full Text] [Related]

  • 20. The nuclear function of p53 is required for PUMA-mediated apoptosis induced by DNA damage.
    Wang P, Yu J, Zhang L.
    Proc Natl Acad Sci U S A; 2007 Mar 06; 104(10):4054-9. PubMed ID: 17360476
    [Abstract] [Full Text] [Related]

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