BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 10446998)

  • 1. Transformation blocks differentiation-induced inhibition of serum response factor interactions with serum response elements.
    Ding W; Witte MM; Scott RE
    Cancer Res; 1999 Aug; 59(15):3795-802. PubMed ID: 10446998
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Selective induction of c-jun and jun-B but not c-fos or c-myc during mitogenesis in SV40-transformed cells at the predifferentiation growth arrest state.
    Wang H; Wang JY; Johnson LR; Scott RE
    Cell Growth Differ; 1991 Dec; 2(12):645-52. PubMed ID: 1667087
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Activation of the c-fos SRE through SAP-1a.
    Masutani H; Magnaghi-Jaulin L; Ait-Si-Ali S; Groisman R; Robin P; Harel-Bellan A
    Oncogene; 1997 Oct; 15(14):1661-9. PubMed ID: 9349499
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phosphorylation of serum response factor by casein kinase II: evidence against a role in growth factor regulation of fos expression.
    Manak JR; Prywes R
    Oncogene; 1993 Mar; 8(3):703-11. PubMed ID: 8437853
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Basic helix-loop-helix proteins can act at the E-box within the serum response element of the c-fos promoter to influence hormone-induced promoter activation in Sertoli cells.
    Chaudhary J; Skinner MK
    Mol Endocrinol; 1999 May; 13(5):774-86. PubMed ID: 10319327
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Decreased expression and activity of the immediate-early growth response (Egr-1) gene product during cellular senescence.
    Meyyappan M; Wheaton K; Riabowol KT
    J Cell Physiol; 1999 Apr; 179(1):29-39. PubMed ID: 10082129
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Two serum response elements mediate transcriptional repression of human smooth muscle alpha-actin promoter in ras-transformed cells.
    Bushel P; Kim JH; Chang W; Catino JJ; Ruley HE; Kumar CC
    Oncogene; 1995 Apr; 10(7):1361-70. PubMed ID: 7731687
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Influence of the glucocorticoid receptor on c-fos inducibility in activated ras-containing mouse lung cells.
    Johnson TA; Li J; Beer DG
    Mol Carcinog; 1996 Oct; 17(2):70-7. PubMed ID: 8890955
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sequences at the 3' side of the c-fos SRE mediate gene expression via an Sob1-dependent, TCF-independent pathway.
    Omoike OI; Benson BA; Chan MA; Benedict SH
    Biochem Biophys Res Commun; 1999 Aug; 262(2):523-9. PubMed ID: 10462507
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Repression of SV40 T oncoprotein expression by DMSO.
    Witte MM; Parker RF; Wang H; Scott RE
    J Cell Physiol; 1992 Apr; 151(1):50-5. PubMed ID: 1373148
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Loss of differentiation control in transformed 3T3 T proadipocytes.
    Sparks RL; Allen BJ; Zygmunt AI; Strauss EE
    Cancer Res; 1993 Apr; 53(8):1770-6. PubMed ID: 8467495
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Insulin-induced mitogenesis associated with transformation by the SV40 large T antigen.
    Wang HL; Scott RE
    J Cell Physiol; 1991 Apr; 147(1):102-10. PubMed ID: 1645356
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Proximal promoter region of the junB gene mediates attenuation of serum inducibility in Src-transformed cells.
    Yu CL; Prochownik EV; Jove R
    Cell Growth Differ; 1995 Dec; 6(12):1513-21. PubMed ID: 9019156
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Downregulation of c-fos gene transcription in cells transformed by E1A and cHa-ras oncogenes: a role of sustained activation of MAP/ERK kinase cascade and of inactive chromatin structure at c-fos promoter.
    Kukushkin AN; Abramova MV; Svetlikova SB; Darieva ZA; Pospelova TV; Pospelov VA
    Oncogene; 2002 Jan; 21(5):719-30. PubMed ID: 11850800
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Differentiation modulates the balance of positive and negative Jun/AP-1 DNA binding activities to regulate cellular proliferative potential: different effects in nontransformed and transformed cells.
    Wang H; Xie Z; Scott RE
    J Cell Biol; 1996 Nov; 135(4):1151-62. PubMed ID: 8922393
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The c-fos serum response element (SRE) confers negative response to glucocorticoids.
    Karagianni N; Tsawdaroglou N
    Oncogene; 1994 Aug; 9(8):2327-34. PubMed ID: 8036015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Senescence represses the nuclear localization of the serum response factor and differentiation regulates its nuclear localization with lineage specificity.
    Ding W; Gao S; Scott RE
    J Cell Sci; 2001 Mar; 114(Pt 5):1011-8. PubMed ID: 11181183
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Role of the TCF phosphorylation state and the chromatin structure in the negative transcription regulation of the c-fos proto-oncogene in E1A + c-Ha-ras transformed cells].
    Abramova MV; Kukushkin AN; Pospelova TV; Svetlikova SB; Pospelov VA
    Mol Biol (Mosk); 2002; 36(1):66-75. PubMed ID: 11862715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Induction of LPL gene expression by sterols is mediated by a sterol regulatory element and is independent of the presence of multiple E boxes.
    Schoonjans K; Gelman L; Haby C; Briggs M; Auwerx J
    J Mol Biol; 2000 Dec; 304(3):323-34. PubMed ID: 11090277
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Crystal structure of a ternary SAP-1/SRF/c-fos SRE DNA complex.
    Mo Y; Ho W; Johnston K; Marmorstein R
    J Mol Biol; 2001 Nov; 314(3):495-506. PubMed ID: 11846562
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.