|1.||Guo, Y: 1 article (03/2000)|
|2.||Wei, L: 1 article (03/2000)|
|3.||Wu, S: 1 article (03/2000)|
|4.||Shen, F: 1 article (03/2000)|
|5.||Liu, Y: 1 article (03/2000)|
|6.||Anthony, D D: 1 article (03/2000)|
|7.||Trojan, J: 1 article (03/2000)|
|8.||Zhao, J: 1 article (03/2000)|
|9.||Habib, N: 1 article (03/2000)|
|10.||Wu, M: 1 article (03/2000)|
03/07/1996 - "MT-PVLT-10 transgenic mice express large T-antigen of polyomavirus under the control of the mouse metallothionein-1 promoter and mates of this transgenic line develop testicular tumors at advanced ages. "
03/01/2000 - "Tumor cells transfected with a vector encoding an IGF-1 antisense cDNA transcriptional cassette driven by the mouse metallothionein-1 promoter become immunogenic and lose their tumorigenicity in syngeneic animals. "
07/01/1997 - "Replacement of the RSV-LTR promoter with the heavy metal-inducible mouse metallothionein-1 promoter in the lacR-responsive unit, as well as the generation of a clonal glioma cell line expressing lacR, did not significantly enhance regulation of DTA in the Lac system. "
01/14/1994 - "Transient expression analyses, however, indicate that this sequence, which contains a core heptanucleotide, TGCACTC, identical to that of the strongest metal regulatory element of the mouse metallothionein-1 gene, is not responsive to Cd2+ or Zn2+. Stable transfection of constructs containing the entire mouse HO-1 gene and various portions of the 5'-flanking region into rat C6 glioma cells and simultaneous, quantitative analysis of the mouse and rat HO-1 mRNAs indicate that distal 5' sequences, between positions -3.5 and -12.5 kbp, are required for induction of mouse HO-1 gene transcription by both heme and heavy metals. "
|2.||Complementary DNA (cDNA)
|3.||Insulin-Like Growth Factor I (IGF-1)
|5.||Tumor Viral Antigens (Large T Antigen)