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2004∼2003

 

110.     Yokoyama, K., Ugai, H., and Murata, T.: “Spontaneous mutations in the human gene for p53 in recombinant adenovirus during multiple passages in 293 cells” Vector Targeting strategies for gene therapy Cold Spring Harbor Meeting, Cold Spring Harbor, NY, pp.47, March (2003).

111.     Fukuda, K., Abei, M., Seo, E., Wakayama, M., Todoroki, T., Hamada, H., Yokoyama, K., and Tanaka, N.: “Combination with chemotherapy enhances efficacy of E1 double-mutant adenovirus for gene therapy of gallbladder cancer” Digestive Disease Week 2003, Orland, FL, May T1174 (2003).

112.     Seo, E., Abei, M., Fukuda, K., Wakayama, M., Ugai, H., Murata, T., Todoroki, T., Hamada, H. and Yokoyama, K.: “Suicide gene therapy gallbladder cancer using a cancer selectively replacing adenovirus carrying uracil phosphoribosyltransferase  (UPRT) gene” Digestive Disease Week 2003, Orland, FL, May T1758 (2003).

113.     Day, N., Ugai, H., Ichiki, A. and Yokoyama, K.: “K-562 cells lack MHC class II expression due to an alternatively spliced cIITA transcript with a truncated coding region.” International Symposium on Molecular Cell Biology of Macrophage 2003, Utsunomiya, Tochigi, Japan, pp.120, June (2003).

114.     Jin C., Li H., Murata, T., Pan, J., Shinozuka, Y., Ugai, H. and Yokoyama, K.: “JDP2, a repressor of AP-1, regulates chromatin remodeling activity associated with histone modification.”  Mechanisms of Eukaryotic Transcription, Cold Spring Harbor Meeting, Cold Spring Harbor, NY, pp.127, Aug. (2003).

115.     Kishikawa, S., Murata, T., Ugai, H., Yamazaki, T. and Yokoyama, K.: “Control elements of Dnmt 1 gene are regulated in cell-cycle dependent manner.” 3rd International Symposium on Nucleic Acids Chemistry.  Sapporo, Hokkaido, Japan, pp.307-308, Sept. (2003).

116.     Kishikawa, S. and Yokoyama, K.: “Control of transcription of the Dnmt 1 gene by Sp1, Sp3 and p300 coactivator.”  Epigenetics, Cold Spring Harbor Meeting, Cold Spring Harbor, NY. pp.114, June (2004).

117.     Jin, C. and Yokoyama, K.: “Transcription factor JDP2 has activities associated with histone modification and nucleosome assembly.” International Symposium on Molecular cell Biology of Macrophage, Osaka, Japan, pp.122, July (2004).

118.     Pan, J., Jin, C., Murata, T. and Yokoyama, K.: “JDP2 mediated-histone modification is critical for regulation of retinoic acid-induced differentiation of F9 Cells.”  Cancer Genetics & Tumor Suppressor Genes, Cold Spring Harbor, NY. pp.165, Aug. (2004).       

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