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Dates: 2001 – 2005

You searched for subject:(Protein Engineering). Showing records 1 – 30 of 33 total matches.

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The Ohio State University

1. Liu, Xinyan. Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity.

Degree: PhD, Ohio State Biochemistry Program, 2005, The Ohio State University

  <i>Bacillus thuringiensis</i>, an aerobic, gram-positive spore-forming bacterium commonly found in soil, produces parasporal crystal (Cry) proteins with insecticidal activity against a wide range of… (more)

Subjects/Keywords: protein-protein interaction; protein engineering

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APA (6th Edition):

Liu, X. (2005). Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918

Chicago Manual of Style (16th Edition):

Liu, Xinyan. “Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity.” 2005. Doctoral Dissertation, The Ohio State University. Accessed July 04, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918.

MLA Handbook (7th Edition):

Liu, Xinyan. “Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity.” 2005. Web. 04 Jul 2020.

Vancouver:

Liu X. Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2020 Jul 04]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918.

Council of Science Editors:

Liu X. Studies of the <i>Manduca sexta</i> cadherin-like receptor binding epitopes of <i>Bacillus thuringiensis</i> Cry1Aa toxin and protein engineering of mosquitocidal activity. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1117655918


Texas A&M University

2. Lum, Karin Tien. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.

Degree: 2004, Texas A&M University

 Directed evolution studies were done with PTE for the enhancement of hydrolysis of both sarin and soman analogs. Particular attention was focused on the toxic… (more)

Subjects/Keywords: protein engineering

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APA (6th Edition):

Lum, K. T. (2004). Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Thesis, Texas A&M University. Accessed July 04, 2020. http://hdl.handle.net/1969.1/149.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Lum, Karin Tien. “Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman.” 2004. Web. 04 Jul 2020.

Vancouver:

Lum KT. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. [Internet] [Thesis]. Texas A&M University; 2004. [cited 2020 Jul 04]. Available from: http://hdl.handle.net/1969.1/149.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Lum KT. Directed evolution of phosphotriesterase: towards the efficient detoxification of sarin and soman. [Thesis]. Texas A&M University; 2004. Available from: http://hdl.handle.net/1969.1/149

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

3. Abdullah, Mohd Amir F. CHARACTERIZATION OF TOXICITY DETERMINANTS IN BACILLUS THURINGIENSIS MOSQUITOCIDAL DELTA-ENDOTOXINS.

Degree: PhD, Biochemistry, 2002, The Ohio State University

 Bacillus thuringiensis mosquitocidal toxin Cry4Ba has no significant natural activity against Culex quinquefasciatus or Cx. pipiens (LC50 >80,000 ng/ml and LC50 >20,000 ng/ml, respectively). We… (more)

Subjects/Keywords: Protein engineering; Bacillus thuringiensis

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APA (6th Edition):

Abdullah, M. A. F. (2002). CHARACTERIZATION OF TOXICITY DETERMINANTS IN BACILLUS THURINGIENSIS MOSQUITOCIDAL DELTA-ENDOTOXINS. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1039312355

Chicago Manual of Style (16th Edition):

Abdullah, Mohd Amir F. “CHARACTERIZATION OF TOXICITY DETERMINANTS IN BACILLUS THURINGIENSIS MOSQUITOCIDAL DELTA-ENDOTOXINS.” 2002. Doctoral Dissertation, The Ohio State University. Accessed July 04, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1039312355.

MLA Handbook (7th Edition):

Abdullah, Mohd Amir F. “CHARACTERIZATION OF TOXICITY DETERMINANTS IN BACILLUS THURINGIENSIS MOSQUITOCIDAL DELTA-ENDOTOXINS.” 2002. Web. 04 Jul 2020.

Vancouver:

Abdullah MAF. CHARACTERIZATION OF TOXICITY DETERMINANTS IN BACILLUS THURINGIENSIS MOSQUITOCIDAL DELTA-ENDOTOXINS. [Internet] [Doctoral dissertation]. The Ohio State University; 2002. [cited 2020 Jul 04]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039312355.

Council of Science Editors:

Abdullah MAF. CHARACTERIZATION OF TOXICITY DETERMINANTS IN BACILLUS THURINGIENSIS MOSQUITOCIDAL DELTA-ENDOTOXINS. [Doctoral Dissertation]. The Ohio State University; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039312355


Penn State University

4. Moore, Gregory Lee. Modeling and Optimization in Directed Evolution Protocols and Protein Engineering.

Degree: PhD, Chemical Engineering, 2005, Penn State University

 The central theme of this thesis aims toward the systematic development of integrated approaches for proactively designing protein libraries with focused diversity for directed evolution… (more)

Subjects/Keywords: directed evolution; protein engineering; optimization

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APA (6th Edition):

Moore, G. L. (2005). Modeling and Optimization in Directed Evolution Protocols and Protein Engineering. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/6525

Chicago Manual of Style (16th Edition):

Moore, Gregory Lee. “Modeling and Optimization in Directed Evolution Protocols and Protein Engineering.” 2005. Doctoral Dissertation, Penn State University. Accessed July 04, 2020. https://etda.libraries.psu.edu/catalog/6525.

MLA Handbook (7th Edition):

Moore, Gregory Lee. “Modeling and Optimization in Directed Evolution Protocols and Protein Engineering.” 2005. Web. 04 Jul 2020.

Vancouver:

Moore GL. Modeling and Optimization in Directed Evolution Protocols and Protein Engineering. [Internet] [Doctoral dissertation]. Penn State University; 2005. [cited 2020 Jul 04]. Available from: https://etda.libraries.psu.edu/catalog/6525.

Council of Science Editors:

Moore GL. Modeling and Optimization in Directed Evolution Protocols and Protein Engineering. [Doctoral Dissertation]. Penn State University; 2005. Available from: https://etda.libraries.psu.edu/catalog/6525


University of New South Wales

5. Chiu, Joyce. Protein engineering of DNA polymerase I: thioredoxin dependent processivity.

Degree: Biotechnology & Biomolecular Sciences, 2005, University of New South Wales

 DNA polymerases are found in a diverse range of organisms, prokaryotes,eukaryotes, viruses and bacteriophage. T7 DNA polymerase is a replicative enzyme from E. coli bacteriophage… (more)

Subjects/Keywords: DNA polymerases; protein engineering; thioredoxin

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APA (6th Edition):

Chiu, J. (2005). Protein engineering of DNA polymerase I: thioredoxin dependent processivity. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/23077 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:831/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Chiu, Joyce. “Protein engineering of DNA polymerase I: thioredoxin dependent processivity.” 2005. Doctoral Dissertation, University of New South Wales. Accessed July 04, 2020. http://handle.unsw.edu.au/1959.4/23077 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:831/SOURCE01?view=true.

MLA Handbook (7th Edition):

Chiu, Joyce. “Protein engineering of DNA polymerase I: thioredoxin dependent processivity.” 2005. Web. 04 Jul 2020.

Vancouver:

Chiu J. Protein engineering of DNA polymerase I: thioredoxin dependent processivity. [Internet] [Doctoral dissertation]. University of New South Wales; 2005. [cited 2020 Jul 04]. Available from: http://handle.unsw.edu.au/1959.4/23077 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:831/SOURCE01?view=true.

Council of Science Editors:

Chiu J. Protein engineering of DNA polymerase I: thioredoxin dependent processivity. [Doctoral Dissertation]. University of New South Wales; 2005. Available from: http://handle.unsw.edu.au/1959.4/23077 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:831/SOURCE01?view=true


Michigan State University

6. Crist, Rachael M. Exploring the underlying chemical basis for color vision : designing a protein mimic of rhodopsin.

Degree: PhD, Department of Chemistry, 2004, Michigan State University

Subjects/Keywords: Color vision; Rhodopsin; Protein engineering

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APA (6th Edition):

Crist, R. M. (2004). Exploring the underlying chemical basis for color vision : designing a protein mimic of rhodopsin. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:47367

Chicago Manual of Style (16th Edition):

Crist, Rachael M. “Exploring the underlying chemical basis for color vision : designing a protein mimic of rhodopsin.” 2004. Doctoral Dissertation, Michigan State University. Accessed July 04, 2020. http://etd.lib.msu.edu/islandora/object/etd:47367.

MLA Handbook (7th Edition):

Crist, Rachael M. “Exploring the underlying chemical basis for color vision : designing a protein mimic of rhodopsin.” 2004. Web. 04 Jul 2020.

Vancouver:

Crist RM. Exploring the underlying chemical basis for color vision : designing a protein mimic of rhodopsin. [Internet] [Doctoral dissertation]. Michigan State University; 2004. [cited 2020 Jul 04]. Available from: http://etd.lib.msu.edu/islandora/object/etd:47367.

Council of Science Editors:

Crist RM. Exploring the underlying chemical basis for color vision : designing a protein mimic of rhodopsin. [Doctoral Dissertation]. Michigan State University; 2004. Available from: http://etd.lib.msu.edu/islandora/object/etd:47367


Penn State University

7. Lehmann, Andreas. Molecular Design in Chemical and Biological Systems.

Degree: PhD, Chemical Engineering, 2004, Penn State University

 The focus of this thesis is the development of methods for computational molecular design with the goal to aid the experimentalist and reduce laboratory cost.… (more)

Subjects/Keywords: quantum chemistry; molecular design; protein design; protein engineering

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APA (6th Edition):

Lehmann, A. (2004). Molecular Design in Chemical and Biological Systems. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/6425

Chicago Manual of Style (16th Edition):

Lehmann, Andreas. “Molecular Design in Chemical and Biological Systems.” 2004. Doctoral Dissertation, Penn State University. Accessed July 04, 2020. https://etda.libraries.psu.edu/catalog/6425.

MLA Handbook (7th Edition):

Lehmann, Andreas. “Molecular Design in Chemical and Biological Systems.” 2004. Web. 04 Jul 2020.

Vancouver:

Lehmann A. Molecular Design in Chemical and Biological Systems. [Internet] [Doctoral dissertation]. Penn State University; 2004. [cited 2020 Jul 04]. Available from: https://etda.libraries.psu.edu/catalog/6425.

Council of Science Editors:

Lehmann A. Molecular Design in Chemical and Biological Systems. [Doctoral Dissertation]. Penn State University; 2004. Available from: https://etda.libraries.psu.edu/catalog/6425


Penn State University

8. Li, Hui. PROTEIN ENGINEERING OF STRUCTURALLY HOMOLOGOUS PROTEINS.

Degree: PhD, Integrative Biosciences, 2005, Penn State University

 One of the ultimate goals of protein engineering is the de novo design of novel proteins with desired activities and properties. However, our current knowledge… (more)

Subjects/Keywords: protein evolution; protein engineering; purine biosynthetic pathway; domain swapping; ; ; )8 barrel protein

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APA (6th Edition):

Li, H. (2005). PROTEIN ENGINEERING OF STRUCTURALLY HOMOLOGOUS PROTEINS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/6804

Chicago Manual of Style (16th Edition):

Li, Hui. “PROTEIN ENGINEERING OF STRUCTURALLY HOMOLOGOUS PROTEINS.” 2005. Doctoral Dissertation, Penn State University. Accessed July 04, 2020. https://etda.libraries.psu.edu/catalog/6804.

MLA Handbook (7th Edition):

Li, Hui. “PROTEIN ENGINEERING OF STRUCTURALLY HOMOLOGOUS PROTEINS.” 2005. Web. 04 Jul 2020.

Vancouver:

Li H. PROTEIN ENGINEERING OF STRUCTURALLY HOMOLOGOUS PROTEINS. [Internet] [Doctoral dissertation]. Penn State University; 2005. [cited 2020 Jul 04]. Available from: https://etda.libraries.psu.edu/catalog/6804.

Council of Science Editors:

Li H. PROTEIN ENGINEERING OF STRUCTURALLY HOMOLOGOUS PROTEINS. [Doctoral Dissertation]. Penn State University; 2005. Available from: https://etda.libraries.psu.edu/catalog/6804


New Jersey Institute of Technology

9. Gautam, Shalini. Optimization of sequential purification of beta-glucosidase from tricoderma reesei in aqueous two-phase system.

Degree: PhD, Chemical Engineering, 2005, New Jersey Institute of Technology

  A novel sequential technique was developed for the purification of a valuable enzyme, beta-glucosidase, from microorganism Tricoderma reesei. The fungus <i>T. reesei</i> produces cellulose… (more)

Subjects/Keywords: Beta-glucosidase; Aqueous two-phase system; Artificial neural networks; Protein purification; Protein partitioning; Protein extraction; Chemical Engineering

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APA (6th Edition):

Gautam, S. (2005). Optimization of sequential purification of beta-glucosidase from tricoderma reesei in aqueous two-phase system. (Doctoral Dissertation). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/dissertations/693

Chicago Manual of Style (16th Edition):

Gautam, Shalini. “Optimization of sequential purification of beta-glucosidase from tricoderma reesei in aqueous two-phase system.” 2005. Doctoral Dissertation, New Jersey Institute of Technology. Accessed July 04, 2020. https://digitalcommons.njit.edu/dissertations/693.

MLA Handbook (7th Edition):

Gautam, Shalini. “Optimization of sequential purification of beta-glucosidase from tricoderma reesei in aqueous two-phase system.” 2005. Web. 04 Jul 2020.

Vancouver:

Gautam S. Optimization of sequential purification of beta-glucosidase from tricoderma reesei in aqueous two-phase system. [Internet] [Doctoral dissertation]. New Jersey Institute of Technology; 2005. [cited 2020 Jul 04]. Available from: https://digitalcommons.njit.edu/dissertations/693.

Council of Science Editors:

Gautam S. Optimization of sequential purification of beta-glucosidase from tricoderma reesei in aqueous two-phase system. [Doctoral Dissertation]. New Jersey Institute of Technology; 2005. Available from: https://digitalcommons.njit.edu/dissertations/693


Georgia Tech

10. Polizzi, Karen Marie. Tools for Maximizing the Efficiency of Protein Engineering.

Degree: PhD, Chemical Engineering, 2005, Georgia Tech

 Biocatalysts offer advantages over their chemical counterparts in terms of their high enantioselectivity and the opportunity to develop more environmentally friendly processes. However, the widespread… (more)

Subjects/Keywords: Pooling; Cloning vector; High-throughput screening; Protein engineering; Biocatalysis; Enzymes; Protein engineering; Biochemical engineering

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APA (6th Edition):

Polizzi, K. M. (2005). Tools for Maximizing the Efficiency of Protein Engineering. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7511

Chicago Manual of Style (16th Edition):

Polizzi, Karen Marie. “Tools for Maximizing the Efficiency of Protein Engineering.” 2005. Doctoral Dissertation, Georgia Tech. Accessed July 04, 2020. http://hdl.handle.net/1853/7511.

MLA Handbook (7th Edition):

Polizzi, Karen Marie. “Tools for Maximizing the Efficiency of Protein Engineering.” 2005. Web. 04 Jul 2020.

Vancouver:

Polizzi KM. Tools for Maximizing the Efficiency of Protein Engineering. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2020 Jul 04]. Available from: http://hdl.handle.net/1853/7511.

Council of Science Editors:

Polizzi KM. Tools for Maximizing the Efficiency of Protein Engineering. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7511


University of Louisville

11. Ahn, Doh Gyeuhn, 1969-. Cost effective human protein C purification from Cohn Fraction IV-1 using mini-antibody.

Degree: PhD, 2005, University of Louisville

Protein C (PC) is an important anticoagulant, antithrombotic, and antiinflammatory in blood plasma. PC deficiency can lead to severe venous thrombotic events, including lung embolism,… (more)

Subjects/Keywords: Protein C; Cohn Fraction IV-1; Miniantibody; Chemical Engineering

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APA (6th Edition):

Ahn, Doh Gyeuhn, 1. (2005). Cost effective human protein C purification from Cohn Fraction IV-1 using mini-antibody. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/19 ; https://ir.library.louisville.edu/etd/19

Chicago Manual of Style (16th Edition):

Ahn, Doh Gyeuhn, 1969-. “Cost effective human protein C purification from Cohn Fraction IV-1 using mini-antibody.” 2005. Doctoral Dissertation, University of Louisville. Accessed July 04, 2020. 10.18297/etd/19 ; https://ir.library.louisville.edu/etd/19.

MLA Handbook (7th Edition):

Ahn, Doh Gyeuhn, 1969-. “Cost effective human protein C purification from Cohn Fraction IV-1 using mini-antibody.” 2005. Web. 04 Jul 2020.

Vancouver:

Ahn, Doh Gyeuhn 1. Cost effective human protein C purification from Cohn Fraction IV-1 using mini-antibody. [Internet] [Doctoral dissertation]. University of Louisville; 2005. [cited 2020 Jul 04]. Available from: 10.18297/etd/19 ; https://ir.library.louisville.edu/etd/19.

Council of Science Editors:

Ahn, Doh Gyeuhn 1. Cost effective human protein C purification from Cohn Fraction IV-1 using mini-antibody. [Doctoral Dissertation]. University of Louisville; 2005. Available from: 10.18297/etd/19 ; https://ir.library.louisville.edu/etd/19


University of Cincinnati

12. Prodan, Bjorg Noah Radu. Modifying Membrane Surfaces via Self-Assembled Monolayers to Reduce Protein Fouling.

Degree: MS, Engineering : Chemical Engineering, 2004, University of Cincinnati

  One of the major factors that limits the use of membranes in many applications involving biological compounds is membrane fouling. Proteins and other biological… (more)

Subjects/Keywords: Engineering, Chemical; self-assembled monolayers; alkanethiols; protein fouling

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APA (6th Edition):

Prodan, B. N. R. (2004). Modifying Membrane Surfaces via Self-Assembled Monolayers to Reduce Protein Fouling. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1091133289

Chicago Manual of Style (16th Edition):

Prodan, Bjorg Noah Radu. “Modifying Membrane Surfaces via Self-Assembled Monolayers to Reduce Protein Fouling.” 2004. Masters Thesis, University of Cincinnati. Accessed July 04, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1091133289.

MLA Handbook (7th Edition):

Prodan, Bjorg Noah Radu. “Modifying Membrane Surfaces via Self-Assembled Monolayers to Reduce Protein Fouling.” 2004. Web. 04 Jul 2020.

Vancouver:

Prodan BNR. Modifying Membrane Surfaces via Self-Assembled Monolayers to Reduce Protein Fouling. [Internet] [Masters thesis]. University of Cincinnati; 2004. [cited 2020 Jul 04]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1091133289.

Council of Science Editors:

Prodan BNR. Modifying Membrane Surfaces via Self-Assembled Monolayers to Reduce Protein Fouling. [Masters Thesis]. University of Cincinnati; 2004. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1091133289


New Jersey Institute of Technology

13. Feins, Meredith Ann. Novel internally-staged ultrafiltration for protein purification.

Degree: PhD, Chemical Engineering, 2004, New Jersey Institute of Technology

  A new ultrafiltration technique based on a multimembrane stack has been developed to fractionate proteins closer in molecular weight than conventionally possible. The technique… (more)

Subjects/Keywords: Ultrafiltration; Membranes; Composite; Protein; Multistaged; Rejection; Chemical Engineering

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APA (6th Edition):

Feins, M. A. (2004). Novel internally-staged ultrafiltration for protein purification. (Doctoral Dissertation). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/dissertations/626

Chicago Manual of Style (16th Edition):

Feins, Meredith Ann. “Novel internally-staged ultrafiltration for protein purification.” 2004. Doctoral Dissertation, New Jersey Institute of Technology. Accessed July 04, 2020. https://digitalcommons.njit.edu/dissertations/626.

MLA Handbook (7th Edition):

Feins, Meredith Ann. “Novel internally-staged ultrafiltration for protein purification.” 2004. Web. 04 Jul 2020.

Vancouver:

Feins MA. Novel internally-staged ultrafiltration for protein purification. [Internet] [Doctoral dissertation]. New Jersey Institute of Technology; 2004. [cited 2020 Jul 04]. Available from: https://digitalcommons.njit.edu/dissertations/626.

Council of Science Editors:

Feins MA. Novel internally-staged ultrafiltration for protein purification. [Doctoral Dissertation]. New Jersey Institute of Technology; 2004. Available from: https://digitalcommons.njit.edu/dissertations/626


Tampere University

14. Hiipakka, Marita. Ligand recognition in SH3-mediated protein interactions .

Degree: Lääketieteellisen teknologian instituutti - Institute of Medical Technology, 2005, Tampere University

 Src homology (SH3) 3-domeenit ovat pieniä, keskimäärin 60 aminohappoa käsittäviä proteiinien toiminnallisia osayksiköitä. Ne säätelevät monia soluille tärkeitä proteiinien välisiä vuorovaikutuksia, erityisesti sellaisia, joilla on… (more)

Subjects/Keywords: Nef; SH3; RT-loop; protein engineering; gene therapy

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APA (6th Edition):

Hiipakka, M. (2005). Ligand recognition in SH3-mediated protein interactions . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/67469

Chicago Manual of Style (16th Edition):

Hiipakka, Marita. “Ligand recognition in SH3-mediated protein interactions .” 2005. Doctoral Dissertation, Tampere University. Accessed July 04, 2020. https://trepo.tuni.fi/handle/10024/67469.

MLA Handbook (7th Edition):

Hiipakka, Marita. “Ligand recognition in SH3-mediated protein interactions .” 2005. Web. 04 Jul 2020.

Vancouver:

Hiipakka M. Ligand recognition in SH3-mediated protein interactions . [Internet] [Doctoral dissertation]. Tampere University; 2005. [cited 2020 Jul 04]. Available from: https://trepo.tuni.fi/handle/10024/67469.

Council of Science Editors:

Hiipakka M. Ligand recognition in SH3-mediated protein interactions . [Doctoral Dissertation]. Tampere University; 2005. Available from: https://trepo.tuni.fi/handle/10024/67469


Texas Tech University

15. Sinha, Archana. Protein engineering on soybean sterol methyl transferase leads to altered substrate binding and catalysis.

Degree: Chemistry, 2004, Texas Tech University

 Sterol methyltransferases (SMTs) are ubiquitously represented in plants and they can serve as the rate-limiting enzymes in the 24-alkyl sterol (phytosterol) pathway. Together these enzymes… (more)

Subjects/Keywords: Alkenes; Protein engineering; Enzymes; Methyltransferases; Amino acids

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APA (6th Edition):

Sinha, A. (2004). Protein engineering on soybean sterol methyl transferase leads to altered substrate binding and catalysis. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/9977

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sinha, Archana. “Protein engineering on soybean sterol methyl transferase leads to altered substrate binding and catalysis.” 2004. Thesis, Texas Tech University. Accessed July 04, 2020. http://hdl.handle.net/2346/9977.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sinha, Archana. “Protein engineering on soybean sterol methyl transferase leads to altered substrate binding and catalysis.” 2004. Web. 04 Jul 2020.

Vancouver:

Sinha A. Protein engineering on soybean sterol methyl transferase leads to altered substrate binding and catalysis. [Internet] [Thesis]. Texas Tech University; 2004. [cited 2020 Jul 04]. Available from: http://hdl.handle.net/2346/9977.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sinha A. Protein engineering on soybean sterol methyl transferase leads to altered substrate binding and catalysis. [Thesis]. Texas Tech University; 2004. Available from: http://hdl.handle.net/2346/9977

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

16. van der Geize, Robert. Engineering of steroid biotransformation in rhodococcus.

Degree: 2002, NARCIS

Subjects/Keywords: Proefschriften (vorm); Protein engineering; Biotransformatie; Steroïden; Actinomyceten; 58.31; 42.33

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APA (6th Edition):

van der Geize, R. (2002). Engineering of steroid biotransformation in rhodococcus. (Doctoral Dissertation). NARCIS. Retrieved from https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; 7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; 11370/7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html

Chicago Manual of Style (16th Edition):

van der Geize, Robert. “Engineering of steroid biotransformation in rhodococcus.” 2002. Doctoral Dissertation, NARCIS. Accessed July 04, 2020. https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; 7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; 11370/7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html.

MLA Handbook (7th Edition):

van der Geize, Robert. “Engineering of steroid biotransformation in rhodococcus.” 2002. Web. 04 Jul 2020.

Vancouver:

van der Geize R. Engineering of steroid biotransformation in rhodococcus. [Internet] [Doctoral dissertation]. NARCIS; 2002. [cited 2020 Jul 04]. Available from: https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; 7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; 11370/7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html.

Council of Science Editors:

van der Geize R. Engineering of steroid biotransformation in rhodococcus. [Doctoral Dissertation]. NARCIS; 2002. Available from: https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; 7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; 11370/7bfd2617-ac87-4ab8-9f07-7c924c15d357 ; urn:nbn:nl:ui:11-dbi/43565cc87929d ; https://www.rug.nl/research/portal/en/publications/engineering-of-steroid-biotransformation-in-rhodococcus(7bfd2617-ac87-4ab8-9f07-7c924c15d357).html


University of the Western Cape

17. Ndabambi, Nonkululeko. Recombinant expression of the pRb- and p53-interacting domains from the human RBBP6 protein for in vitro binding studies .

Degree: 2004, University of the Western Cape

 This thesis describes the cloning and recombinant expression of domains from the human RBBP6 protein for future in vitro binding studies with pRb and p53.… (more)

Subjects/Keywords: Recombinant proteins; Proteins; Biotechnology; Protein engineering; Genetic vectors

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APA (6th Edition):

Ndabambi, N. (2004). Recombinant expression of the pRb- and p53-interacting domains from the human RBBP6 protein for in vitro binding studies . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/1685

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ndabambi, Nonkululeko. “Recombinant expression of the pRb- and p53-interacting domains from the human RBBP6 protein for in vitro binding studies .” 2004. Thesis, University of the Western Cape. Accessed July 04, 2020. http://hdl.handle.net/11394/1685.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ndabambi, Nonkululeko. “Recombinant expression of the pRb- and p53-interacting domains from the human RBBP6 protein for in vitro binding studies .” 2004. Web. 04 Jul 2020.

Vancouver:

Ndabambi N. Recombinant expression of the pRb- and p53-interacting domains from the human RBBP6 protein for in vitro binding studies . [Internet] [Thesis]. University of the Western Cape; 2004. [cited 2020 Jul 04]. Available from: http://hdl.handle.net/11394/1685.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ndabambi N. Recombinant expression of the pRb- and p53-interacting domains from the human RBBP6 protein for in vitro binding studies . [Thesis]. University of the Western Cape; 2004. Available from: http://hdl.handle.net/11394/1685

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Georgia Tech

18. Schwimmer, Lauren J. Engineering ligand-receptor pairs for small molecule control of transcription.

Degree: PhD, Chemistry and Biochemistry, 2005, Georgia Tech

 Creating receptors for control of transcription with arbitrary small molecules has widespread applications including gene therapy, biosensors, and enzyme engineering. Using the combination of high… (more)

Subjects/Keywords: Chemical complementation; Ligand-receptor pair; Protein engineering; Retinoid X receptor; Nuclear receptor; Codon randomized libraries; Transcription factors; Protein engineering; Nuclear receptors (Biochemistry); Genetic engineering

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APA (6th Edition):

Schwimmer, L. J. (2005). Engineering ligand-receptor pairs for small molecule control of transcription. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11651

Chicago Manual of Style (16th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Doctoral Dissertation, Georgia Tech. Accessed July 04, 2020. http://hdl.handle.net/1853/11651.

MLA Handbook (7th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Web. 04 Jul 2020.

Vancouver:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2020 Jul 04]. Available from: http://hdl.handle.net/1853/11651.

Council of Science Editors:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/11651

19. Yu, Zhongshui. Spray freezing into liquid to produce protein microparticles.

Degree: PhD, Pharmacy, 2004, University of Texas – Austin

 Recent advances in molecular biology have led to an explosive growth in the number of peptide and protein drugs derived from both recombinant technology and… (more)

Subjects/Keywords: Particle engineering processes; Protein stability; Spray freezing into liquid; Protein microparticles; Peptide drug delivery systems; SFL

…process is an effective particle engineering process for protein and peptide pharmaceuticals… …xvii CHAPTER 1: Particle Engineering Technologies for Protein and Peptide Pharmaceuticals… …205 UT xx CHAPTER 1: Particle Engineering Technologies for Protein and Peptide… …engineering technology. Firstly, the use of the SFL process to produce peptide microparticles was… …used to produce protein microparticles. In the study, bovine serum albumin (BSA), a… 

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Yu, Z. (2004). Spray freezing into liquid to produce protein microparticles. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/29918

Chicago Manual of Style (16th Edition):

Yu, Zhongshui. “Spray freezing into liquid to produce protein microparticles.” 2004. Doctoral Dissertation, University of Texas – Austin. Accessed July 04, 2020. http://hdl.handle.net/2152/29918.

MLA Handbook (7th Edition):

Yu, Zhongshui. “Spray freezing into liquid to produce protein microparticles.” 2004. Web. 04 Jul 2020.

Vancouver:

Yu Z. Spray freezing into liquid to produce protein microparticles. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2004. [cited 2020 Jul 04]. Available from: http://hdl.handle.net/2152/29918.

Council of Science Editors:

Yu Z. Spray freezing into liquid to produce protein microparticles. [Doctoral Dissertation]. University of Texas – Austin; 2004. Available from: http://hdl.handle.net/2152/29918


Florida State University

20. [No author]. A Redesigned Hydrophobic Core of a Symmetric Protein Superfold with Increased Primary Structure Symmetry.

Degree: 2004, Florida State University

Human acidic fibroblast growth factor (FGF-1) is a member of the £]-trefoil superfamily and exhibits a characteristic three-fold tertiary structure symmetry. However, evidence of this… (more)

Subjects/Keywords: Chemistry and Biochemistry, Department of; protein evolution; de novo design; protein engineering; beta-trefoil

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APA (6th Edition):

author], [. (2004). A Redesigned Hydrophobic Core of a Symmetric Protein Superfold with Increased Primary Structure Symmetry. (Thesis). Florida State University. Retrieved from http://purl.flvc.org/fcla/dt/121313 ;

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

author], [No. “A Redesigned Hydrophobic Core of a Symmetric Protein Superfold with Increased Primary Structure Symmetry.” 2004. Thesis, Florida State University. Accessed July 04, 2020. http://purl.flvc.org/fcla/dt/121313 ;.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

author], [No. “A Redesigned Hydrophobic Core of a Symmetric Protein Superfold with Increased Primary Structure Symmetry.” 2004. Web. 04 Jul 2020.

Vancouver:

author] [. A Redesigned Hydrophobic Core of a Symmetric Protein Superfold with Increased Primary Structure Symmetry. [Internet] [Thesis]. Florida State University; 2004. [cited 2020 Jul 04]. Available from: http://purl.flvc.org/fcla/dt/121313 ;.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

author] [. A Redesigned Hydrophobic Core of a Symmetric Protein Superfold with Increased Primary Structure Symmetry. [Thesis]. Florida State University; 2004. Available from: http://purl.flvc.org/fcla/dt/121313 ;

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Kentucky

21. Hart, Amanda Peter. BONE ENGINEERING OF THE ULNA OF RABBIT.

Degree: 2005, University of Kentucky

 Repair of bone defects is a major challenge in orthopaedic surgery. Current bone graft treatments, including autografts, allografts and xenografts, have many limitations making it… (more)

Subjects/Keywords: tissue engineering scaffold; nanocomposite; bone morphogenetic protein-2; segmental defect; bone regeneration

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APA (6th Edition):

Hart, A. P. (2005). BONE ENGINEERING OF THE ULNA OF RABBIT. (Masters Thesis). University of Kentucky. Retrieved from http://uknowledge.uky.edu/gradschool_theses/199

Chicago Manual of Style (16th Edition):

Hart, Amanda Peter. “BONE ENGINEERING OF THE ULNA OF RABBIT.” 2005. Masters Thesis, University of Kentucky. Accessed July 04, 2020. http://uknowledge.uky.edu/gradschool_theses/199.

MLA Handbook (7th Edition):

Hart, Amanda Peter. “BONE ENGINEERING OF THE ULNA OF RABBIT.” 2005. Web. 04 Jul 2020.

Vancouver:

Hart AP. BONE ENGINEERING OF THE ULNA OF RABBIT. [Internet] [Masters thesis]. University of Kentucky; 2005. [cited 2020 Jul 04]. Available from: http://uknowledge.uky.edu/gradschool_theses/199.

Council of Science Editors:

Hart AP. BONE ENGINEERING OF THE ULNA OF RABBIT. [Masters Thesis]. University of Kentucky; 2005. Available from: http://uknowledge.uky.edu/gradschool_theses/199


New Jersey Institute of Technology

22. Xu, Yanke. Studies on improved integrated membrane-based chromatographic process for bioseparation.

Degree: PhD, Chemical Engineering, 2004, New Jersey Institute of Technology

  To improve protein separation and purification directly from a fermentation broth, a novel membrane filtration-cum-chromatography device configuration having a relatively impermeable coated zone near… (more)

Subjects/Keywords: Bioseparation; Protein purification; Chromatography; Membrane filtration; Interfacial polymerization; Chemical Engineering

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APA (6th Edition):

Xu, Y. (2004). Studies on improved integrated membrane-based chromatographic process for bioseparation. (Doctoral Dissertation). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/dissertations/616

Chicago Manual of Style (16th Edition):

Xu, Yanke. “Studies on improved integrated membrane-based chromatographic process for bioseparation.” 2004. Doctoral Dissertation, New Jersey Institute of Technology. Accessed July 04, 2020. https://digitalcommons.njit.edu/dissertations/616.

MLA Handbook (7th Edition):

Xu, Yanke. “Studies on improved integrated membrane-based chromatographic process for bioseparation.” 2004. Web. 04 Jul 2020.

Vancouver:

Xu Y. Studies on improved integrated membrane-based chromatographic process for bioseparation. [Internet] [Doctoral dissertation]. New Jersey Institute of Technology; 2004. [cited 2020 Jul 04]. Available from: https://digitalcommons.njit.edu/dissertations/616.

Council of Science Editors:

Xu Y. Studies on improved integrated membrane-based chromatographic process for bioseparation. [Doctoral Dissertation]. New Jersey Institute of Technology; 2004. Available from: https://digitalcommons.njit.edu/dissertations/616

23. Tang, Lixia. Kinetic analysis and protein engineering of halohydrin dehalogenase.

Degree: 2004, NARCIS

Subjects/Keywords: Proefschriften (vorm); Epichloorhydrine; Agrobacterium; Dynamica; Dehalogenases; Protein engineering; vitaminen (biochemie); hormonen; enzymen

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APA (6th Edition):

Tang, L. (2004). Kinetic analysis and protein engineering of halohydrin dehalogenase. (Doctoral Dissertation). NARCIS. Retrieved from https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; 0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; 11370/0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; urn:isbn:9036721016 ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html

Chicago Manual of Style (16th Edition):

Tang, Lixia. “Kinetic analysis and protein engineering of halohydrin dehalogenase.” 2004. Doctoral Dissertation, NARCIS. Accessed July 04, 2020. https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; 0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; 11370/0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; urn:isbn:9036721016 ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html.

MLA Handbook (7th Edition):

Tang, Lixia. “Kinetic analysis and protein engineering of halohydrin dehalogenase.” 2004. Web. 04 Jul 2020.

Vancouver:

Tang L. Kinetic analysis and protein engineering of halohydrin dehalogenase. [Internet] [Doctoral dissertation]. NARCIS; 2004. [cited 2020 Jul 04]. Available from: https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; 0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; 11370/0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; urn:isbn:9036721016 ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html.

Council of Science Editors:

Tang L. Kinetic analysis and protein engineering of halohydrin dehalogenase. [Doctoral Dissertation]. NARCIS; 2004. Available from: https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; 0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; 11370/0b72ec53-01df-4da5-836f-f2d2d27bf7cc ; urn:isbn:9036721016 ; urn:nbn:nl:ui:11-dbi/4b1cdd145fe29 ; https://www.rug.nl/research/portal/en/publications/kinetic-analysis-and-protein-engineering-of-halohydrin-dehalogenase(0b72ec53-01df-4da5-836f-f2d2d27bf7cc).html


Indian Institute of Science

24. Kumaran, M. Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods.

Degree: 2004, Indian Institute of Science

Subjects/Keywords: MutL Homologs 1p Interacting Proteins - Biochemical Methods; Protein Engineering; Genetic Engineering; MLH Ip; mMLH1 cDNA; Biochemical Genetics

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APA (6th Edition):

Kumaran, M. (2004). Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/1154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kumaran, M. “Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods.” 2004. Thesis, Indian Institute of Science. Accessed July 04, 2020. http://hdl.handle.net/2005/1154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kumaran, M. “Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods.” 2004. Web. 04 Jul 2020.

Vancouver:

Kumaran M. Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods. [Internet] [Thesis]. Indian Institute of Science; 2004. [cited 2020 Jul 04]. Available from: http://hdl.handle.net/2005/1154.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kumaran M. Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods. [Thesis]. Indian Institute of Science; 2004. Available from: http://hdl.handle.net/2005/1154

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Indian Institute of Science

25. Kumaran, M. Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods.

Degree: 2004, Indian Institute of Science

Subjects/Keywords: MutL Homologs 1p Interacting Proteins - Biochemical Methods; Protein Engineering; Genetic Engineering; MLH Ip; mMLH1 cDNA; Biochemical Genetics

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APA (6th Edition):

Kumaran, M. (2004). Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/1154 ; http://etd.ncsi.iisc.ernet.in/abstracts/1510/G18455-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kumaran, M. “Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods.” 2004. Thesis, Indian Institute of Science. Accessed July 04, 2020. http://etd.iisc.ernet.in/handle/2005/1154 ; http://etd.ncsi.iisc.ernet.in/abstracts/1510/G18455-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kumaran, M. “Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods.” 2004. Web. 04 Jul 2020.

Vancouver:

Kumaran M. Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods. [Internet] [Thesis]. Indian Institute of Science; 2004. [cited 2020 Jul 04]. Available from: http://etd.iisc.ernet.in/handle/2005/1154 ; http://etd.ncsi.iisc.ernet.in/abstracts/1510/G18455-Abs.pdf.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Kumaran M. Identification Of Novel MLH 1p Interacting Proteins By Biochemical And Genetic Methods. [Thesis]. Indian Institute of Science; 2004. Available from: http://etd.iisc.ernet.in/handle/2005/1154 ; http://etd.ncsi.iisc.ernet.in/abstracts/1510/G18455-Abs.pdf

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Oulu

26. Kiema, T.-R. (Tiila-Riikka). Studies on the peroxisomal multifunctional enzyme type-1:domain structure with special reference to the hydratase/isomerase fold.

Degree: 2001, University of Oulu

 Abstract The peroxisomal multifunctional enzyme type-1 (perMFE-1) is a monomeric protein of β-oxidation possessing 2-enoyl-CoA hydratase-1, Δ3-Δ 2-enoyl-CoA isomerase, and (3S)-hydroxyacyl-CoA dehydrogenase activities. The amino-terminal… (more)

Subjects/Keywords: 2-enoyl-CoA hydratase; 3-hydroxyacyl-CoA dehydrogenase; b-oxidation; enoyl-CoA isomerase; protein engineering

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APA (6th Edition):

Kiema, T. -. (. (2001). Studies on the peroxisomal multifunctional enzyme type-1:domain structure with special reference to the hydratase/isomerase fold. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9514265777

Chicago Manual of Style (16th Edition):

Kiema, T -R (Tiila-Riikka). “Studies on the peroxisomal multifunctional enzyme type-1:domain structure with special reference to the hydratase/isomerase fold.” 2001. Doctoral Dissertation, University of Oulu. Accessed July 04, 2020. http://urn.fi/urn:isbn:9514265777.

MLA Handbook (7th Edition):

Kiema, T -R (Tiila-Riikka). “Studies on the peroxisomal multifunctional enzyme type-1:domain structure with special reference to the hydratase/isomerase fold.” 2001. Web. 04 Jul 2020.

Vancouver:

Kiema T-(. Studies on the peroxisomal multifunctional enzyme type-1:domain structure with special reference to the hydratase/isomerase fold. [Internet] [Doctoral dissertation]. University of Oulu; 2001. [cited 2020 Jul 04]. Available from: http://urn.fi/urn:isbn:9514265777.

Council of Science Editors:

Kiema T-(. Studies on the peroxisomal multifunctional enzyme type-1:domain structure with special reference to the hydratase/isomerase fold. [Doctoral Dissertation]. University of Oulu; 2001. Available from: http://urn.fi/urn:isbn:9514265777


Vanderbilt University

27. Cao, Shang. Non-redundant functions of the mouse Ssrp1 and Pfdn1 genes revealed by gene targeting and gene entrapment.

Degree: PhD, Microbiology and Immunology, 2005, Vanderbilt University

 NON-REDUNDANT FUNCTIONS OF THE MOUSE SSRP1 AND PFDN1 GENES REVEALED BY GENE TARGETING AND GENE ENTRAPMENT SHANG CAO Dissertation under the direction of Professor Henry… (more)

Subjects/Keywords: Mice  – Genetic engineering; Pfdn1; Ssrp1; protein folding; cytoskeleton; chromain remodeling; gene trap; knockout mouse model; Proteins  – Analysis; Gene targeting

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Cao, S. (2005). Non-redundant functions of the mouse Ssrp1 and Pfdn1 genes revealed by gene targeting and gene entrapment. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11302005-194329/ ;

Chicago Manual of Style (16th Edition):

Cao, Shang. “Non-redundant functions of the mouse Ssrp1 and Pfdn1 genes revealed by gene targeting and gene entrapment.” 2005. Doctoral Dissertation, Vanderbilt University. Accessed July 04, 2020. http://etd.library.vanderbilt.edu/available/etd-11302005-194329/ ;.

MLA Handbook (7th Edition):

Cao, Shang. “Non-redundant functions of the mouse Ssrp1 and Pfdn1 genes revealed by gene targeting and gene entrapment.” 2005. Web. 04 Jul 2020.

Vancouver:

Cao S. Non-redundant functions of the mouse Ssrp1 and Pfdn1 genes revealed by gene targeting and gene entrapment. [Internet] [Doctoral dissertation]. Vanderbilt University; 2005. [cited 2020 Jul 04]. Available from: http://etd.library.vanderbilt.edu/available/etd-11302005-194329/ ;.

Council of Science Editors:

Cao S. Non-redundant functions of the mouse Ssrp1 and Pfdn1 genes revealed by gene targeting and gene entrapment. [Doctoral Dissertation]. Vanderbilt University; 2005. Available from: http://etd.library.vanderbilt.edu/available/etd-11302005-194329/ ;

28. Pikkemaat, Mariël Gertrude. New insight in haloalkane dehalogenase kinetics and evolution by enzyme engineering.

Degree: 2004, NARCIS

Subjects/Keywords: Proefschriften (vorm); Protein engineering; Haloalkaan dehalogenase; Moleculaire dynamica; nucleïnezuren; eiwitten; vitaminen (biochemie); hormonen; enzymen

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Pikkemaat, M. G. (2004). New insight in haloalkane dehalogenase kinetics and evolution by enzyme engineering. (Doctoral Dissertation). NARCIS. Retrieved from https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; ba34a52d-2160-4180-b2b3-302fdac7347c ; 11370/ba34a52d-2160-4180-b2b3-302fdac7347c ; urn:isbn:9036720524 ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html

Chicago Manual of Style (16th Edition):

Pikkemaat, Mariël Gertrude. “New insight in haloalkane dehalogenase kinetics and evolution by enzyme engineering.” 2004. Doctoral Dissertation, NARCIS. Accessed July 04, 2020. https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; ba34a52d-2160-4180-b2b3-302fdac7347c ; 11370/ba34a52d-2160-4180-b2b3-302fdac7347c ; urn:isbn:9036720524 ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html.

MLA Handbook (7th Edition):

Pikkemaat, Mariël Gertrude. “New insight in haloalkane dehalogenase kinetics and evolution by enzyme engineering.” 2004. Web. 04 Jul 2020.

Vancouver:

Pikkemaat MG. New insight in haloalkane dehalogenase kinetics and evolution by enzyme engineering. [Internet] [Doctoral dissertation]. NARCIS; 2004. [cited 2020 Jul 04]. Available from: https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; ba34a52d-2160-4180-b2b3-302fdac7347c ; 11370/ba34a52d-2160-4180-b2b3-302fdac7347c ; urn:isbn:9036720524 ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html.

Council of Science Editors:

Pikkemaat MG. New insight in haloalkane dehalogenase kinetics and evolution by enzyme engineering. [Doctoral Dissertation]. NARCIS; 2004. Available from: https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; ba34a52d-2160-4180-b2b3-302fdac7347c ; 11370/ba34a52d-2160-4180-b2b3-302fdac7347c ; urn:isbn:9036720524 ; urn:nbn:nl:ui:11-dbi/4b1ccf517327f ; https://www.rug.nl/research/portal/en/publications/new-insight-in-haloalkane-dehalogenase-kinetics-and-evolution-by-enzyme-engineering(ba34a52d-2160-4180-b2b3-302fdac7347c).html

29. Biesebeke, te, R. Molecular analysis and improvement of protein production by Aspergillus oryzae grown on solid substrates.

Degree: 2005, NARCIS

Subjects/Keywords: aspergillus flavus var. oryzae; eiwitsecretie; aminozuursequenties; Genetische modificatie; aspergillus flavus var. oryzae; protein secretion; amino acid sequences; Genetic Engineering

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Biesebeke, te, R. (2005). Molecular analysis and improvement of protein production by Aspergillus oryzae grown on solid substrates. (Doctoral Dissertation). NARCIS. Retrieved from http://library.wur.nl/WebQuery/wurpubs/338223 ; urn:nbn:nl:ui:32-338223 ; urn:nbn:nl:ui:32-338223 ; http://library.wur.nl/WebQuery/wurpubs/338223

Chicago Manual of Style (16th Edition):

Biesebeke, te, R. “Molecular analysis and improvement of protein production by Aspergillus oryzae grown on solid substrates.” 2005. Doctoral Dissertation, NARCIS. Accessed July 04, 2020. http://library.wur.nl/WebQuery/wurpubs/338223 ; urn:nbn:nl:ui:32-338223 ; urn:nbn:nl:ui:32-338223 ; http://library.wur.nl/WebQuery/wurpubs/338223.

MLA Handbook (7th Edition):

Biesebeke, te, R. “Molecular analysis and improvement of protein production by Aspergillus oryzae grown on solid substrates.” 2005. Web. 04 Jul 2020.

Vancouver:

Biesebeke, te R. Molecular analysis and improvement of protein production by Aspergillus oryzae grown on solid substrates. [Internet] [Doctoral dissertation]. NARCIS; 2005. [cited 2020 Jul 04]. Available from: http://library.wur.nl/WebQuery/wurpubs/338223 ; urn:nbn:nl:ui:32-338223 ; urn:nbn:nl:ui:32-338223 ; http://library.wur.nl/WebQuery/wurpubs/338223.

Council of Science Editors:

Biesebeke, te R. Molecular analysis and improvement of protein production by Aspergillus oryzae grown on solid substrates. [Doctoral Dissertation]. NARCIS; 2005. Available from: http://library.wur.nl/WebQuery/wurpubs/338223 ; urn:nbn:nl:ui:32-338223 ; urn:nbn:nl:ui:32-338223 ; http://library.wur.nl/WebQuery/wurpubs/338223

30. Kaper, T. Engineering of β-glycosidases from hyperthermophilic Archaea.

Degree: 2001, NARCIS

 <FONT FACE="MS Sans Serif" SIZE=2> Hyperthermophilic Archaea are microorganisms that grow optimally above 80°C. To be able to live at these temperature extremes their cell… (more)

Subjects/Keywords: glycosidasen; thermofiele micro-organismen; eiwittechnologie; Moleculaire biologie (algemeen); glycosidases; thermophilic microorganisms; protein engineering; Molecular Biology (General)

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Kaper, T. (2001). Engineering of β-glycosidases from hyperthermophilic Archaea. (Doctoral Dissertation). NARCIS. Retrieved from http://library.wur.nl/WebQuery/wurpubs/110249 ; urn:nbn:nl:ui:32-110249 ; urn:nbn:nl:ui:32-110249 ; http://library.wur.nl/WebQuery/wurpubs/110249

Chicago Manual of Style (16th Edition):

Kaper, T. “Engineering of β-glycosidases from hyperthermophilic Archaea.” 2001. Doctoral Dissertation, NARCIS. Accessed July 04, 2020. http://library.wur.nl/WebQuery/wurpubs/110249 ; urn:nbn:nl:ui:32-110249 ; urn:nbn:nl:ui:32-110249 ; http://library.wur.nl/WebQuery/wurpubs/110249.

MLA Handbook (7th Edition):

Kaper, T. “Engineering of β-glycosidases from hyperthermophilic Archaea.” 2001. Web. 04 Jul 2020.

Vancouver:

Kaper T. Engineering of β-glycosidases from hyperthermophilic Archaea. [Internet] [Doctoral dissertation]. NARCIS; 2001. [cited 2020 Jul 04]. Available from: http://library.wur.nl/WebQuery/wurpubs/110249 ; urn:nbn:nl:ui:32-110249 ; urn:nbn:nl:ui:32-110249 ; http://library.wur.nl/WebQuery/wurpubs/110249.

Council of Science Editors:

Kaper T. Engineering of β-glycosidases from hyperthermophilic Archaea. [Doctoral Dissertation]. NARCIS; 2001. Available from: http://library.wur.nl/WebQuery/wurpubs/110249 ; urn:nbn:nl:ui:32-110249 ; urn:nbn:nl:ui:32-110249 ; http://library.wur.nl/WebQuery/wurpubs/110249

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