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Kiyotaka Shiba

Division of Protein Engineering

Cancer Institute

Japanese Foundation for Cancer Research

Koto, Tokyo 135-8550

Japan

[email]@jfcr.or.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Division of Protein Engineering, Cancer Institute, Japanese Foundation for Cancer Research, Koto, Tokyo 135-8550, Japan. 1998 - 2011

References

  1. Creation of novel signalling modulators from existing cytokine using scanning motif-programming. Murakami, T., Kashiwagi, K., Shiba, K. Chem. Commun. (Camb.) (2011) [Pubmed]
  2. Natural and artificial peptide motifs: their origins and the application of motif-programming. Shiba, K. Chem. Soc. Rev (2010) [Pubmed]
  3. Functionalization of carbon nanomaterials by evolutionary molecular engineering: potential application in drug delivery systems. Shiba, K. J. Drug. Target (2006) [Pubmed]
  4. Distinct macroscopic structures developed from solutions of chemical compounds and periodic proteins. Shiba, K., Honma, T., Minamisawa, T., Nishiguchi, K., Noda, T. EMBO Rep. (2003) [Pubmed]
  5. Translated products of tandem microgene repeats exhibit diverse properties also seen in natural proteins. Shiba, K., Shirai, T., Honma, T., Noda, T. Protein Eng. (2003) [Pubmed]
  6. On the role of periodism in the origin of proteins. Shiba, K., Takahashi, Y., Noda, T. J. Mol. Biol. (2002) [Pubmed]
  7. Guide oligonucleotide-dependent DNA linkage that facilitates controllable polymerization of microgene blocks. Shiba, K., Hatada, T., Takahashi, Y., Noda, T. J. Biochem. (2002) [Pubmed]
  8. Intron positions delineate the evolutionary path of a pervasively appended peptide in five human aminoacyl-tRNA synthetases. Shiba, K. J. Mol. Evol. (2002) [Pubmed]
  9. Human asparaginyl-tRNA synthetase: molecular cloning and the inference of the evolutionary history of Asx-tRNA synthetase family. Shiba, K., Motegi, H., Yoshida, M., Noda, T. Nucleic Acids Res. (1998) [Pubmed]
 
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