N. Ohnishi

High expression of transgenes mediated by hybrid retroviral vectors in hepatocytes: comparison of promoters from murine retroviruses in vitro and in vivo

T. Okanoue, C. Baum, J. Fujita, 2002, Gene Therapy.

Retroviral vector-mediated gene expression in human CD34+CD38- cells expanded in vitro: cis elements of FMEV are superior to those of Mo-MuLV.

W. Ostertag, C. Baum, K. Tomiwa, 2000, Human gene therapy.

Combination of non-natural D-amino acid derivatives and allophenylnorstatine-dimethylthioproline scaffold in HIV protease inhibitors have high efficacy in mutant HIV.

Y. Kiso, Y. Hamada, Tooru Kimura, 2008, Journal of medicinal chemistry.

Efficient gene transfer by hybrid retroviral vectors to murine spermatogenic cells.

W. Ostertag, C. Baum, K. Tomiwa, 1999, Human gene therapy.

Ink4a/Arf−/− and HRAS(G12V) transform mouse mammary cells into triple-negative breast cancer containing tumorigenic CD49f− quiescent cells

G. Hortobagyi, L. Pusztai, H. Saya, 2013, Oncogene.

cells into triple-negative breast cancer containing tumorigenic CD49fquiescent cells

G. Hortobagyi, L. Pusztai, H. Saya, 2013 .