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Naruya Tomita

Department of Geriatric Medicine

Osaka University Graduate School of Medicine

2-15 Yamada-oka

Suita 565-0871

Japan

[email]@*.med.osaka-u.ac.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Geriatric Medicine, Osaka University Graduate School of Medicine, 2-15 Yamada-oka, Suita 565-0871, Japan. 2002 - 2004
  • Department of General Medicine, Osaka University Hospital, Suita, Japan. 2001 - 2003

References

  1. Antisense oligonucleotides as a powerful molecular strategy for gene therapy in cardiovascular diseases. Tomita, N., Morishita, R. Curr. Pharm. Des. (2004) [Pubmed]
  2. Gene therapy with an E2F transcription factor decoy inhibits cell cycle progression in rat anti-Thy 1 glomerulonephritis. Tomita, N., Kim, J.Y., Gibbons, G.H., Zhang, L., Kaneda, Y., Stahl, R.A., Ogborn, M., Venderville, B., Morishita, R., Baran, D., Dzau, V.J. Int. J. Mol. Med. (2004) [Pubmed]
  3. Application of decoy oligodeoxynucleotides-based approach to renal diseases. Tomita, N., Azuma, H., Kaneda, Y., Ogihara, T., Morishita, R. Curr. Drug. Targets (2004) [Pubmed]
  4. Gene therapy with transcription factor decoy oligonucleotides as a potential treatment for cardiovascular diseases. Tomita, N., Azuma, H., Kaneda, Y., Ogihara, T., Morishita, R. Curr. Drug. Targets (2003) [Pubmed]
  5. Development of novel decoy oligonucleotides: advantages of circular dumb-bell decoy. Tomita, N., Tomita, T., Yuyama, K., Tougan, T., Tajima, T., Ogihara, T., Morishita, R. Curr. Opin. Mol. Ther. (2003) [Pubmed]
  6. Transcription factors as molecular targets: molecular mechanisms of decoy ODN and their design. Tomita, N., Ogihara, T., Morishita, R. Curr. Drug. Targets (2003) [Pubmed]
  7. Therapeutic potential of decoy oligonucleotides strategy in cardiovascular diseases. Tomita, N., Ogihara, T., Morishita, R. Expert. Rev. Cardiovasc. Ther (2003) [Pubmed]
  8. Potential therapeutic applications of decoy oligonucleotides. Tomita, N., Morishita, R., Tomita, T., Ogihara, T. Curr. Opin. Mol. Ther. (2002) [Pubmed]
  9. Therapeutic approach to familial hypercholesterolemia by HVJ-liposomes in LDL receptor knockout mouse. Tomita, N., Morishita, R., Koike, H., Hashizume, M., Notake, M., Fujitani, B., Kaneda, Y., Horiuchi, M., Ogihara, T. Int. J. Mol. Med. (2002) [Pubmed]
  10. Targeted gene therapy for rat glomerulonephritis using HVJ-immunoliposomes. Tomita, N., Morishita, R., Yamamoto, K., Higaki, J., Dzau, V.J., Ogihara, T., Kaneda, Y. J. Gene. Med (2002) [Pubmed]
  11. Inhibition of TNF-alpha, induced cytokine and adhesion molecule. Expression in glomerular cells in vitro and in vivo by transcription factor decoy for NFkappaB. Tomita, N., Morishita, R., Tomita, S., Kaneda, Y., Higaki, J., Ogihara, T., Horiuchi, M. Exp. Nephrol. (2001) [Pubmed]
  12. A family with von Hippel-Lindau disease revealed by pheochromocytoma. Tomita, N., Moriguchi, A., Yamasaki, K., Taniyama, Y., Kotani, N., Hashiya, N., Yoshida, M., Yao, M., Higaki, J., Ogihara, T. Hypertens. Res. (2001) [Pubmed]
 
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