BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 6092929)

  • 1. Less than 40% of the simian virus 40 large T-antigen-coding sequence is required for transformation.
    Sompayrac L; Danna KJ
    Mol Cell Biol; 1984 Aug; 4(8):1661-3. PubMed ID: 6092929
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Simian virus 40 sequences between 0.168 and 0.424 map units are not required for abortive transformation.
    Sompayrac LM; Danna KJ
    J Virol; 1983 May; 46(2):475-80. PubMed ID: 6302314
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The simian virus 40 sequences between 0.169 and 0.423 map units are not essential to immortalize early-passage rat embryo cells.
    Sompayrac L; Danna KJ
    Mol Cell Biol; 1985 May; 5(5):1191-4. PubMed ID: 2987680
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Simian virus 40 large T-antigen point mutants that are defective in viral DNA replication but competent in oncogenic transformation.
    Manos MM; Gluzman Y
    Mol Cell Biol; 1984 Jun; 4(6):1125-33. PubMed ID: 6330530
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expression of simian virus 40 large T antigen in embryonal carcinoma cell hybrids.
    Tunnacliffe A; Crawford LV; Goodfellow P
    Mol Cell Biol; 1984 Aug; 4(8):1657-60. PubMed ID: 6149461
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An SV40 mutant T antigen does not bind the SV40 viral origin.
    Sompayrac L; Danna KJ
    Virology; 1986 Sep; 153(2):297-309. PubMed ID: 3016992
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Transformation by purified early genes of simian virus 40.
    Chang LS; Pater MM; Hutchinson NI; di Mayorca G
    Virology; 1984 Mar; 133(2):341-53. PubMed ID: 6324456
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic and biochemical analysis of transformation-competent, replication-defective simian virus 40 large T antigen mutants.
    Manos MM; Gluzman Y
    J Virol; 1985 Jan; 53(1):120-7. PubMed ID: 2981330
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Conversion through homologous recombination of the gene encoding Simian virus 40 115,000-molecular-weight super T antigen to a gene encoding a normal-size large T antigen variant.
    May P; Resche-Rigon M; Borde J; Breugnot C; May E
    Mol Cell Biol; 1984 Jun; 4(6):1141-51. PubMed ID: 6330531
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The t-unique coding domain is important to the transformation maintenance function of the simian virus 40 small t antigen.
    Bikel I; Mamon H; Brown EL; Boltax J; Agha M; Livingston DM
    Mol Cell Biol; 1986 Apr; 6(4):1172-8. PubMed ID: 3023875
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletion of 43 amino acids in the NH2-terminal half of the large tumor antigen of simian virus 40 results in a non-karyophilic protein capable of transforming established cells.
    Fischer-Fantuzzi L; Vesco C
    Proc Natl Acad Sci U S A; 1985 Apr; 82(7):1891-5. PubMed ID: 2984671
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Deletion mutations in the small t antigen gene alter the tissue specificity of tumors induced by simian virus 40.
    Matthews BJ; Levine AS; Dixon K
    J Virol; 1987 Apr; 61(4):1282-5. PubMed ID: 3029426
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Large T antigens of simian virus 40 and polyomavirus efficiently establish primary fibroblasts.
    Jat PS; Sharp PA
    J Virol; 1986 Sep; 59(3):746-50. PubMed ID: 3016337
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Recombinant retroviruses encoding simian virus 40 large T antigen and polyomavirus large and middle T antigens.
    Jat PS; Cepko CL; Mulligan RC; Sharp PA
    Mol Cell Biol; 1986 Apr; 6(4):1204-17. PubMed ID: 3023876
    [TBL] [Abstract][Full Text] [Related]  

  • 15. trans-dominant defective mutants of simian virus 40 T antigen.
    Farber JM; Peden KW; Nathans D
    J Virol; 1987 Feb; 61(2):436-45. PubMed ID: 3027373
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Immunologic selection of simian virus 40 (SV40) T-antigen-negative tumor cells which arise by excision of early SV40 DNA.
    Mora PT; Parrott CL; Baksi K; McFarland V
    J Virol; 1986 Sep; 59(3):628-34. PubMed ID: 3016325
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Stabilization of the 53,000-dalton nonviral tumor antigen is not required for transformation by simian virus 40.
    Sompayrac LM; Gurney EG; Danna KJ
    Mol Cell Biol; 1983 Feb; 3(2):290-6. PubMed ID: 6300663
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations near the carboxyl terminus of the simian virus 40 large tumor antigen alter viral host range.
    Pipas JM
    J Virol; 1985 May; 54(2):569-75. PubMed ID: 2985819
    [TBL] [Abstract][Full Text] [Related]  

  • 19. N-terminal amino acid sequences of the polyoma middle-size T antigen are important for protein kinase activity and cell transformation.
    Templeton D; Eckhart W
    Mol Cell Biol; 1984 May; 4(5):817-21. PubMed ID: 6328268
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Simian virus 40 T antigen is required for viral excision from chromosomes.
    Miller J; Bullock P; Botchan M
    Proc Natl Acad Sci U S A; 1984 Dec; 81(23):7534-8. PubMed ID: 6095304
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.