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Cha, H.J., Hwang, D.S., Lim, S., White, J.D., Matos-Perez C.R., and Wilker, J.J.,"Bulk adhesive strength of recombinant hybrid mussel adhesive protein", Biofouling(ISSN 0892-7014), Vol.25(2), pp.99-107 Taylor & Francis Group (2009.02).
Ref: Bulk adhesive strength of recombinant hybrid mussel adhesive protein.pdf
Hwang, D.S., Kim, K.R., Lim, S., Choi, Y.S., and Cha, H.J., "Recombinant Mussel Adhesive Protein as a Gene Delivery Material", Biotechnology and Bioengineering(ISSN 0006-3592), Vol.102(2), pp.616-623 WILEY (2009.02).
Ref: Recombinant Mussel Adhesive Protein as a Gene Delivery Material.pdf
Garcia, J.R., Cha, H.J., Rao, G., Marten, M.R., and Bentley, W.E., "Microbial nar-GFP cell sensors reveal oxygen limitations in highly agitated and aerated laboratory-scale fermentors", Microbial Cell Factories(ISSN 1475-2859), Vol.8:6 BioMed Central (2009.01).
Ref: Microbial nar-GFP cell sensors reveal oxygen limitations in highly agitated and aerated laboratory-scale fermentors.pdf
Gim, Y., Hwang, D.S., Lim, S., Song, Y.H., and Cha, H.J., "Production of fusion Mussel Adhesive fp-353 in Escherichia coli", Biotechnology Progress(ISSN 8756-7938), Vol.24(6), pp.1272-1277 ACS Publications (2008.12).
Ref: Production of Fusion Mussel Adhesive fp-353 in Escherichia coli.pdf
Dennison, S.R., Kim, Y.S., Cha, H.J., and Phoenix, D.A., "Investigations into the ability of the peptide, HAL18, to interact with bacterial membranes", European Biophysics Journal(ISSN 0175-7571), Vol.38(1), pp.37-43 Springer Berlin/Heidelberg (2008.11).
Ref: Investigations into the ability of the peptide HAL18 to interact with bacterial membranes.pdf
Kim, Y.S., and Cha, H.J., "Facile Evaluation of Cell Disruption Efficiency Using pH-Controlled Fluorescence Resonance Energy Transfer", Biotechnology Progress(ISSN 8756-7938), Vol.24(5), pp.1186-1190 ACS Publications (2008.10).
Ref: Facile Evaluation of Cell Disruption Efficiency Using pH-Controlled Fluorescence Resonance Energy Transfer.pdf
Kang, D.G., Li L., Ha, J.H., Choi, S.S., and Cha, H.J., "Efficient cell surface display of organophosphorous hydrolase using N-terminal domain of ice nucleation protein in Escherichia coli", Korean Journal of Chemical Engineering(ISSN 0256-1115), Vol.25(4), pp.804-807 Springer New York (2008.07).
Ref: Efficient cell surface display of OPH using N-terminal domain of ice nucleation protein in Ecoli.pdf
Hwang, B.H., and Cha, H.J., "Quantitative oligonucleotide microarray data analysis with an artificial standard probe strategy", Biosensors and Bioelectronics(ISSN 0956-5663), Vol.23(11), pp.1738-1744 Elsevier (2008.06).
Ref: Quantitative oligonucleotide microarray data analysis with an artificial standard probe strategy.pdf
Kim, D., Hwang, D.S., Kang, D.G., Kim, J.Y.H., and Cha, H.J., "Enhancement of Mussel Adhesive Protein Production in Escherichia coli by Co-expression of Bacterial Hemoglobin", Biotechnology Progress(ISSN 8756-7938), Vol.24(3), pp.663-666 ACS Publications (2008.06).
Ref: Enhancement of MAP Production in Ecoli by Co-expression of VHb.pdf
Bae, E., Lee, J.W., Hwang, B.H., Yeo, J., Yoon, J., Cha, H.J., and Choi, W., "Photocatalytic Bacterial Inactivation by Polyoxometalates", Chemosphere(ISSN 0045-6535), Vol.72(2), pp.174-181 Elsevier (2008.05).
Ref: Photocatalytic bacterial inactivation by polyoxometalates.pdf
     
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Depart of Chemical Engineering, POSTECH San 31 Hyoja-dong Nam-gu Pohang, Kyungbuk, 790-784, Korea
Tel.+82-54-279-2280(English), 5951(Korean) Fax.+82-54-279-5528 E-mail.hjcha@postech.ac.kr