BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 8659116)

  • 1. Gain of Sp1 sites and loss of repressor sequences associated with a young, transcriptionally active subset of HERV-H endogenous long terminal repeats.
    Nelson DT; Goodchild NL; Mager DL
    Virology; 1996 Jun; 220(1):213-8. PubMed ID: 8659116
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Comparative analyses of LTRs of the ERV-H family of primate-specific retrovirus-like elements isolated from marmoset, African green monkey, and man.
    Anderssen S; Sjøttem E; Svineng G; Johansen T
    Virology; 1997 Jul; 234(1):14-30. PubMed ID: 9234943
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The promoter activity of long terminal repeats of the HERV-H family of human retrovirus-like elements is critically dependent on Sp1 family proteins interacting with a GC/GT box located immediately 3' to the TATA box.
    Sjøttem E; Anderssen S; Johansen T
    J Virol; 1996 Jan; 70(1):188-98. PubMed ID: 8523525
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Functional activity of HERV-K-T47D-related long terminal repeats.
    Baust C; Seifarth W; Schön U; Hehlmann R; Leib-Mösch C
    Virology; 2001 May; 283(2):262-72. PubMed ID: 11336551
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Recent evolutionary expansion of a subfamily of RTVL-H human endogenous retrovirus-like elements.
    Goodchild NL; Wilkinson DA; Mager DL
    Virology; 1993 Oct; 196(2):778-88. PubMed ID: 8372448
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Regulation of KLF5 involves the Sp1 transcription factor in human epithelial cells.
    Chen C; Zhou Y; Zhou Z; Sun X; Otto KB; Uht RM; Dong JT
    Gene; 2004 Apr; 330():133-42. PubMed ID: 15087132
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genomic distribution and transcription of solitary HERV-K LTRs.
    Leib-Mösch C; Haltmeier M; Werner T; Geigl EM; Brack-Werner R; Francke U; Erfle V; Hehlmann R
    Genomics; 1993 Nov; 18(2):261-9. PubMed ID: 8288228
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Structural characteristics of four long terminal repeats (LTR) of human endogenous retroviruses and features of their integration sites].
    Khil' PP; Kostina MB; Azhikina TL; Kolesnik TB; Lebedev IuB; Sverdlov ED
    Bioorg Khim; 1997 May; 23(5):434-40. PubMed ID: 9290053
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cell type-specific expression and promoter activity of human endogenous retroviral long terminal repeats.
    Schön U; Seifarth W; Baust C; Hohenadl C; Erfle V; Leib-Mösch C
    Virology; 2001 Jan; 279(1):280-91. PubMed ID: 11145909
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sp1/Sp3 and the myeloid zinc finger gene MZF1 regulate the human N-cadherin promoter in osteoblasts.
    Le Mée S; Fromigué O; Marie PJ
    Exp Cell Res; 2005 Jan; 302(1):129-42. PubMed ID: 15541732
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Transcriptional regulation of the hepatocyte growth factor (HGF) gene by the Sp family of transcription factors.
    Jiang JG; Chen Q; Bell A; Zarnegar R
    Oncogene; 1997 Jun; 14(25):3039-49. PubMed ID: 9223667
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Characterization of the human topoisomerase IIbeta (TOP2B) promoter activity: essential roles of the nuclear factor-Y (NF-Y)- and specificity protein-1 (Sp1)-binding sites.
    Lok CN; Lang AJ; Mirski SE; Cole SP
    Biochem J; 2002 Dec; 368(Pt 3):741-51. PubMed ID: 12197834
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of the promoter of human transcription factor Sp3 and evidence of the role of factors Sp1 and Sp3 in the expression of Sp3 protein.
    Lou Z; Maher VM; McCormick JJ
    Gene; 2005 May; 351():51-9. PubMed ID: 15857802
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sp1/Sp3 and DNA-methylation contribute to basal transcriptional activation of human podoplanin in MG63 versus Saos-2 osteoblastic cells.
    Hantusch B; Kalt R; Krieger S; Puri C; Kerjaschki D
    BMC Mol Biol; 2007 Mar; 8():20. PubMed ID: 17343736
    [TBL] [Abstract][Full Text] [Related]  

  • 15. At least 50% of human-specific HERV-K (HML-2) long terminal repeats serve in vivo as active promoters for host nonrepetitive DNA transcription.
    Buzdin A; Kovalskaya-Alexandrova E; Gogvadze E; Sverdlov E
    J Virol; 2006 Nov; 80(21):10752-62. PubMed ID: 17041225
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cloning and analysis of rat osteoclast inhibitory lectin gene promoter.
    Quan JX; Zheng F; Li XX; Hu LL; Sun ZY; Jiao YL; Wang BL
    J Cell Biochem; 2009 Mar; 106(4):599-607. PubMed ID: 19127542
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional characterization of the human SOX3 promoter: identification of transcription factors implicated in basal promoter activity.
    Kovacevic Grujicic N; Mojsin M; Krstic A; Stevanovic M
    Gene; 2005 Jan; 344():287-97. PubMed ID: 15656994
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sp1 and AP2 enhance promoter activity of the mouse GM3-synthase gene.
    Xia T; Zeng G; Gao L; Yu RK
    Gene; 2005 May; 351():109-18. PubMed ID: 15890474
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The transcriptional activity of HERV-I LTR is negatively regulated by its cis-elements and wild type p53 tumor suppressor protein.
    Chang NT; Yang WK; Huang HC; Yeh KW; Wu CW
    J Biomed Sci; 2007 Mar; 14(2):211-22. PubMed ID: 17151828
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Regulation of the human transforming growth factor beta type II receptor gene promoter by novel Sp1 sites.
    Jennings R; Alsarraj M; Wright KL; Muñoz-Antonia T
    Oncogene; 2001 Oct; 20(47):6899-909. PubMed ID: 11687969
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.