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You searched for subject:(fusion protein). Showing records 1 – 30 of 178 total matches.

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Addis Ababa University

1. LIKU, BEKELE. EVALUATION OF SEROLOGICAL RESPONSE TO ONCOPROTEINS OF HUMAN PAPILLOMAVIRUS TYPES 16 AND 18 AS POTENTIAL SEROMARKERS FOR CERVICAL CANCER SCREENING .

Degree: 2008, Addis Ababa University

 Cervical cancer is a serious public health problem of global importance. Nearly 80% of the half-a-million new cases reported annually occur in developing countries. The… (more)

Subjects/Keywords: ELISA; GST fusion protein; HPV; Cervical cancer

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

APA (6th Edition):

LIKU, B. (2008). EVALUATION OF SEROLOGICAL RESPONSE TO ONCOPROTEINS OF HUMAN PAPILLOMAVIRUS TYPES 16 AND 18 AS POTENTIAL SEROMARKERS FOR CERVICAL CANCER SCREENING . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/553

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):

LIKU, BEKELE. “EVALUATION OF SEROLOGICAL RESPONSE TO ONCOPROTEINS OF HUMAN PAPILLOMAVIRUS TYPES 16 AND 18 AS POTENTIAL SEROMARKERS FOR CERVICAL CANCER SCREENING .” 2008. Thesis, Addis Ababa University. Accessed April 18, 2021. http://etd.aau.edu.et/dspace/handle/123456789/553.

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

MLA Handbook (7th Edition):

LIKU, BEKELE. “EVALUATION OF SEROLOGICAL RESPONSE TO ONCOPROTEINS OF HUMAN PAPILLOMAVIRUS TYPES 16 AND 18 AS POTENTIAL SEROMARKERS FOR CERVICAL CANCER SCREENING .” 2008. Web. 18 Apr 2021.

Vancouver:

LIKU B. EVALUATION OF SEROLOGICAL RESPONSE TO ONCOPROTEINS OF HUMAN PAPILLOMAVIRUS TYPES 16 AND 18 AS POTENTIAL SEROMARKERS FOR CERVICAL CANCER SCREENING . [Internet] [Thesis]. Addis Ababa University; 2008. [cited 2021 Apr 18]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/553.

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

Council of Science Editors:

LIKU B. EVALUATION OF SEROLOGICAL RESPONSE TO ONCOPROTEINS OF HUMAN PAPILLOMAVIRUS TYPES 16 AND 18 AS POTENTIAL SEROMARKERS FOR CERVICAL CANCER SCREENING . [Thesis]. Addis Ababa University; 2008. Available from: http://etd.aau.edu.et/dspace/handle/123456789/553

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


University of Washington

2. Vulovic, Ivan. Software Algorithms for Design of Symmetric Protein Complexes Applied to Cryo-Electron Microscopy Scaffolds and Antibody Nanoparticles.

Degree: PhD, 2020, University of Washington

 Innovation in the symmetric assembly and protein material design space has the potential to – eventually – reinvent medicine and nanotechnology. One leading strategy for… (more)

Subjects/Keywords: genetic fusion; protein design; Biochemistry; Molecular engineering

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APA (6th Edition):

Vulovic, I. (2020). Software Algorithms for Design of Symmetric Protein Complexes Applied to Cryo-Electron Microscopy Scaffolds and Antibody Nanoparticles. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/45809

Chicago Manual of Style (16th Edition):

Vulovic, Ivan. “Software Algorithms for Design of Symmetric Protein Complexes Applied to Cryo-Electron Microscopy Scaffolds and Antibody Nanoparticles.” 2020. Doctoral Dissertation, University of Washington. Accessed April 18, 2021. http://hdl.handle.net/1773/45809.

MLA Handbook (7th Edition):

Vulovic, Ivan. “Software Algorithms for Design of Symmetric Protein Complexes Applied to Cryo-Electron Microscopy Scaffolds and Antibody Nanoparticles.” 2020. Web. 18 Apr 2021.

Vancouver:

Vulovic I. Software Algorithms for Design of Symmetric Protein Complexes Applied to Cryo-Electron Microscopy Scaffolds and Antibody Nanoparticles. [Internet] [Doctoral dissertation]. University of Washington; 2020. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1773/45809.

Council of Science Editors:

Vulovic I. Software Algorithms for Design of Symmetric Protein Complexes Applied to Cryo-Electron Microscopy Scaffolds and Antibody Nanoparticles. [Doctoral Dissertation]. University of Washington; 2020. Available from: http://hdl.handle.net/1773/45809


University of Southern California

3. Chen, Xiaoying. Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics.

Degree: PhD, Pharmaceutical Sciences, 2011, University of Southern California

 Recombinant fusion proteins have become an important class of biomolecules since the invention of recombinant DNA technology. As an indispensable component of recombinant fusion proteins,… (more)

Subjects/Keywords: linker; fusion protein; transferrin; pharmacokinetics; pharmacodynamics

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APA (6th Edition):

Chen, X. (2011). Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837

Chicago Manual of Style (16th Edition):

Chen, Xiaoying. “Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics.” 2011. Doctoral Dissertation, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837.

MLA Handbook (7th Edition):

Chen, Xiaoying. “Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics.” 2011. Web. 18 Apr 2021.

Vancouver:

Chen X. Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837.

Council of Science Editors:

Chen X. Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837


University of Vienna

4. Kitzler, Christian Manuel. Investigating the binding-site and possible long-range effects of the interaction between BRCA1 and MAX-MAX using NMR spectroscopy.

Degree: 2019, University of Vienna

In dieser Arbeit wurde die Bindungsstelle zwischen BRCA1 und MAX-MAX mittels NMR untersucht. Weiters wurde ein großes intrinsisch ungeordnetes Fragment von BRCA1 durch Fusion von… (more)

Subjects/Keywords: 42.13 Molekularbiologie; Protein Interaktion / BRCA1 / MAX / IDP / NMR / Protein Fusion; Protein interaction / BRCA1 / MAX / IDP / NMR / protein fusion

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

APA (6th Edition):

Kitzler, C. M. (2019). Investigating the binding-site and possible long-range effects of the interaction between BRCA1 and MAX-MAX using NMR spectroscopy. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/56339/

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):

Kitzler, Christian Manuel. “Investigating the binding-site and possible long-range effects of the interaction between BRCA1 and MAX-MAX using NMR spectroscopy.” 2019. Thesis, University of Vienna. Accessed April 18, 2021. http://othes.univie.ac.at/56339/.

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

MLA Handbook (7th Edition):

Kitzler, Christian Manuel. “Investigating the binding-site and possible long-range effects of the interaction between BRCA1 and MAX-MAX using NMR spectroscopy.” 2019. Web. 18 Apr 2021.

Vancouver:

Kitzler CM. Investigating the binding-site and possible long-range effects of the interaction between BRCA1 and MAX-MAX using NMR spectroscopy. [Internet] [Thesis]. University of Vienna; 2019. [cited 2021 Apr 18]. Available from: http://othes.univie.ac.at/56339/.

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

Council of Science Editors:

Kitzler CM. Investigating the binding-site and possible long-range effects of the interaction between BRCA1 and MAX-MAX using NMR spectroscopy. [Thesis]. University of Vienna; 2019. Available from: http://othes.univie.ac.at/56339/

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


Temple University

5. Cheong, Jae Eun. DEVELOPMENT OF SPIROLIGOMER SCAFFOLDS FOR INHIBITING HIV FUSION AND POROUS ORGANIC POLYMERS.

Degree: PhD, 2016, Temple University

Chemistry

This research presents a new approach to creating large, complex molecules to carry out molecular recognition and catalytic functions mimicking biological proteins. Development of… (more)

Subjects/Keywords: Chemistry;

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

APA (6th Edition):

Cheong, J. E. (2016). DEVELOPMENT OF SPIROLIGOMER SCAFFOLDS FOR INHIBITING HIV FUSION AND POROUS ORGANIC POLYMERS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,406966

Chicago Manual of Style (16th Edition):

Cheong, Jae Eun. “DEVELOPMENT OF SPIROLIGOMER SCAFFOLDS FOR INHIBITING HIV FUSION AND POROUS ORGANIC POLYMERS.” 2016. Doctoral Dissertation, Temple University. Accessed April 18, 2021. http://digital.library.temple.edu/u?/p245801coll10,406966.

MLA Handbook (7th Edition):

Cheong, Jae Eun. “DEVELOPMENT OF SPIROLIGOMER SCAFFOLDS FOR INHIBITING HIV FUSION AND POROUS ORGANIC POLYMERS.” 2016. Web. 18 Apr 2021.

Vancouver:

Cheong JE. DEVELOPMENT OF SPIROLIGOMER SCAFFOLDS FOR INHIBITING HIV FUSION AND POROUS ORGANIC POLYMERS. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2021 Apr 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,406966.

Council of Science Editors:

Cheong JE. DEVELOPMENT OF SPIROLIGOMER SCAFFOLDS FOR INHIBITING HIV FUSION AND POROUS ORGANIC POLYMERS. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,406966


University of the Western Cape

6. Choi, Yook-Wah. Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus .

Degree: 2011, University of the Western Cape

 Hepatitis C was first recognized as a transfusion-associated liver disease not caused by hepatitis A or hepatitis B virus after serological tests were developed to… (more)

Subjects/Keywords: Hepatitis C virus (HCV); GST fusion protein; NS5B; Protein crystallisation screens

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APA (6th Edition):

Choi, Y. (2011). Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/5299

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):

Choi, Yook-Wah. “Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus .” 2011. Thesis, University of the Western Cape. Accessed April 18, 2021. http://hdl.handle.net/11394/5299.

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

MLA Handbook (7th Edition):

Choi, Yook-Wah. “Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus .” 2011. Web. 18 Apr 2021.

Vancouver:

Choi Y. Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus . [Internet] [Thesis]. University of the Western Cape; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/11394/5299.

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

Council of Science Editors:

Choi Y. Structural and functional characterization of human DDX5 and its interaction with NS5B of hepatitis C virus . [Thesis]. University of the Western Cape; 2011. Available from: http://hdl.handle.net/11394/5299

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


University of Southern California

7. Chen, Yu-Sheng. Production and characterization of proinsulin-transferrin fusion protein.

Degree: MS, Pharmaceutical Sciences, 2011, University of Southern California

 A transferrin-based fusion protein, proinsulin-transferrin (ProIns-Tf) had been constructed using recombinant protein technology in our laboratory. Based on the in vitro preliminary results, ProIns-Tf reduced… (more)

Subjects/Keywords: bifunctional fusion protein; his-tag; insulin; proinsulin; protein purification; transferrin

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APA (6th Edition):

Chen, Y. (2011). Production and characterization of proinsulin-transferrin fusion protein. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258

Chicago Manual of Style (16th Edition):

Chen, Yu-Sheng. “Production and characterization of proinsulin-transferrin fusion protein.” 2011. Masters Thesis, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258.

MLA Handbook (7th Edition):

Chen, Yu-Sheng. “Production and characterization of proinsulin-transferrin fusion protein.” 2011. Web. 18 Apr 2021.

Vancouver:

Chen Y. Production and characterization of proinsulin-transferrin fusion protein. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258.

Council of Science Editors:

Chen Y. Production and characterization of proinsulin-transferrin fusion protein. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258


IUPUI

8. Ettaki, Zacharia Nabil. Developing Novel Methods to Identify RNA-Associated Mechanisms for Inheritance.

Degree: 2020, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Animals depend on inheriting non-genetic information early in life to grow and develop naturally. This inherited, non-genetic information was previously… (more)

Subjects/Keywords: RNA; Protein; Halo; SNAP; Fusion Protein; Inheritance; RNA-binding protein; crystal; structure; antibody

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APA (6th Edition):

Ettaki, Z. N. (2020). Developing Novel Methods to Identify RNA-Associated Mechanisms for Inheritance. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/24500

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):

Ettaki, Zacharia Nabil. “Developing Novel Methods to Identify RNA-Associated Mechanisms for Inheritance.” 2020. Thesis, IUPUI. Accessed April 18, 2021. http://hdl.handle.net/1805/24500.

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

MLA Handbook (7th Edition):

Ettaki, Zacharia Nabil. “Developing Novel Methods to Identify RNA-Associated Mechanisms for Inheritance.” 2020. Web. 18 Apr 2021.

Vancouver:

Ettaki ZN. Developing Novel Methods to Identify RNA-Associated Mechanisms for Inheritance. [Internet] [Thesis]. IUPUI; 2020. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1805/24500.

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

Council of Science Editors:

Ettaki ZN. Developing Novel Methods to Identify RNA-Associated Mechanisms for Inheritance. [Thesis]. IUPUI; 2020. Available from: http://hdl.handle.net/1805/24500

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

9. Peláez, Miguel Ángel Postigo. Construction of a Fusion Gene : to anchor a truncated version of the inflammatory receptor NLRP3 to the cell membrane.

Degree: Bioscience, 2019, University of Skövde

  Inflammasomes are a group of protein complex that regulate inflammation throughcomplex signal transduction, although their specific mechanisms and structures have notbeen fully described. As… (more)

Subjects/Keywords: NLRP3; Inflammation; Fusion gene; PCR; Fusion protein; Biochemistry and Molecular Biology; Biokemi och molekylärbiologi

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APA (6th Edition):

Peláez, M. . P. (2019). Construction of a Fusion Gene : to anchor a truncated version of the inflammatory receptor NLRP3 to the cell membrane. (Thesis). University of Skövde. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17573

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):

Peláez, Miguel Ángel Postigo. “Construction of a Fusion Gene : to anchor a truncated version of the inflammatory receptor NLRP3 to the cell membrane.” 2019. Thesis, University of Skövde. Accessed April 18, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17573.

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

MLA Handbook (7th Edition):

Peláez, Miguel Ángel Postigo. “Construction of a Fusion Gene : to anchor a truncated version of the inflammatory receptor NLRP3 to the cell membrane.” 2019. Web. 18 Apr 2021.

Vancouver:

Peláez MP. Construction of a Fusion Gene : to anchor a truncated version of the inflammatory receptor NLRP3 to the cell membrane. [Internet] [Thesis]. University of Skövde; 2019. [cited 2021 Apr 18]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17573.

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

Council of Science Editors:

Peláez MP. Construction of a Fusion Gene : to anchor a truncated version of the inflammatory receptor NLRP3 to the cell membrane. [Thesis]. University of Skövde; 2019. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17573

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


Rice University

10. Desai, Tanvi. Characterization of Structure and Function Relationship between Domains of the ER Membrane Protein Atlastin.

Degree: PhD, Natural Sciences, 2014, Rice University

 The endoplasmic Reticulum (ER) is an important site for lipid synthesis, protein synthesis and transport. ER fusion is an essential process for its maintenance and… (more)

Subjects/Keywords: Membrane fusion; Membrane protein; Atlastin; Endoplasmic reticulum; Hereditary spastic paraplegia; Intracellular fusion; Axonal neuropathy

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APA (6th Edition):

Desai, T. (2014). Characterization of Structure and Function Relationship between Domains of the ER Membrane Protein Atlastin. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/76430

Chicago Manual of Style (16th Edition):

Desai, Tanvi. “Characterization of Structure and Function Relationship between Domains of the ER Membrane Protein Atlastin.” 2014. Doctoral Dissertation, Rice University. Accessed April 18, 2021. http://hdl.handle.net/1911/76430.

MLA Handbook (7th Edition):

Desai, Tanvi. “Characterization of Structure and Function Relationship between Domains of the ER Membrane Protein Atlastin.” 2014. Web. 18 Apr 2021.

Vancouver:

Desai T. Characterization of Structure and Function Relationship between Domains of the ER Membrane Protein Atlastin. [Internet] [Doctoral dissertation]. Rice University; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1911/76430.

Council of Science Editors:

Desai T. Characterization of Structure and Function Relationship between Domains of the ER Membrane Protein Atlastin. [Doctoral Dissertation]. Rice University; 2014. Available from: http://hdl.handle.net/1911/76430


North Carolina State University

11. Choi, Ucheor B. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.

Degree: PhD, Physics, 2010, North Carolina State University

 Conformational information about proteins can often reveal the mechanisms of their biological functions. This thesis examines conformational aspects of the synaptic SNARE (soluble N-ethylmaleimide-sensitive factor… (more)

Subjects/Keywords: protein-protein interactions; synaptic vesicle; single molecule FRET; neurotransmitter release; membrane fusion

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APA (6th Edition):

Choi, U. B. (2010). Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/6220

Chicago Manual of Style (16th Edition):

Choi, Ucheor B. “Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.” 2010. Doctoral Dissertation, North Carolina State University. Accessed April 18, 2021. http://www.lib.ncsu.edu/resolver/1840.16/6220.

MLA Handbook (7th Edition):

Choi, Ucheor B. “Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.” 2010. Web. 18 Apr 2021.

Vancouver:

Choi UB. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. [Internet] [Doctoral dissertation]. North Carolina State University; 2010. [cited 2021 Apr 18]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6220.

Council of Science Editors:

Choi UB. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. [Doctoral Dissertation]. North Carolina State University; 2010. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6220

12. Tilbury, Maura A. The expression of recombinant proteins with biomedical importance in Escherichia coli.

Degree: 2020, NUI Galway

 Naturally-occurring peptides and proteins with diverse biological roles have enormous potential for use as therapeutics and biomaterials. While proteins of biomedical interest were traditionally isolated… (more)

Subjects/Keywords: Escherichia coli; recombinant protein; barnacle; adhesion; functional amyloid; fusion protein; superoxide dismutase; Microbiology; Natural Sciences

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APA (6th Edition):

Tilbury, M. A. (2020). The expression of recombinant proteins with biomedical importance in Escherichia coli. (Thesis). NUI Galway. Retrieved from http://hdl.handle.net/10379/16104

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):

Tilbury, Maura A. “The expression of recombinant proteins with biomedical importance in Escherichia coli.” 2020. Thesis, NUI Galway. Accessed April 18, 2021. http://hdl.handle.net/10379/16104.

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

MLA Handbook (7th Edition):

Tilbury, Maura A. “The expression of recombinant proteins with biomedical importance in Escherichia coli.” 2020. Web. 18 Apr 2021.

Vancouver:

Tilbury MA. The expression of recombinant proteins with biomedical importance in Escherichia coli. [Internet] [Thesis]. NUI Galway; 2020. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10379/16104.

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

Council of Science Editors:

Tilbury MA. The expression of recombinant proteins with biomedical importance in Escherichia coli. [Thesis]. NUI Galway; 2020. Available from: http://hdl.handle.net/10379/16104

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


University of Illinois – Chicago

13. Klosterman, Susan M. Control of Synaptic Transmission Through SNARE Complex Regulation.

Degree: 2013, University of Illinois – Chicago

 Synaptic transmission requires the assembly of a highly conserved complex composed of the SNARE proteins Syntaxin, SNAP-25, and Synaptobrevin. The Syntaxin binding protein Tomosyn has… (more)

Subjects/Keywords: Synaptic transmission; Soluble N-ethylmaleimide sensitive fusion protein (NSF) Attachment Protein Receptor (SNARES)

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APA (6th Edition):

Klosterman, S. M. (2013). Control of Synaptic Transmission Through SNARE Complex Regulation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10043

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):

Klosterman, Susan M. “Control of Synaptic Transmission Through SNARE Complex Regulation.” 2013. Thesis, University of Illinois – Chicago. Accessed April 18, 2021. http://hdl.handle.net/10027/10043.

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

MLA Handbook (7th Edition):

Klosterman, Susan M. “Control of Synaptic Transmission Through SNARE Complex Regulation.” 2013. Web. 18 Apr 2021.

Vancouver:

Klosterman SM. Control of Synaptic Transmission Through SNARE Complex Regulation. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10027/10043.

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

Council of Science Editors:

Klosterman SM. Control of Synaptic Transmission Through SNARE Complex Regulation. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10043

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


University of Cincinnati

14. Gow, Chien-Hung, M.D. Novel mechanisms of transcriptional regulation by leukemia fusion proteins.

Degree: PhD, Medicine: Cancer and Cell Biology, 2014, University of Cincinnati

 Transcription factors and chromatin structure are master regulators of homeostasis during hematopoiesis. Regulatory genes for each stage of hematopoiesis are activated or silenced in a… (more)

Subjects/Keywords: Oncology; transcriptional regulation; leukemia fusion protein; E-protein; E2A-Pbx1; AML1-ETO; HDAC3

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APA (6th Edition):

Gow, Chien-Hung, M. D. (2014). Novel mechanisms of transcriptional regulation by leukemia fusion proteins. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980

Chicago Manual of Style (16th Edition):

Gow, Chien-Hung, M D. “Novel mechanisms of transcriptional regulation by leukemia fusion proteins.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed April 18, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980.

MLA Handbook (7th Edition):

Gow, Chien-Hung, M D. “Novel mechanisms of transcriptional regulation by leukemia fusion proteins.” 2014. Web. 18 Apr 2021.

Vancouver:

Gow, Chien-Hung MD. Novel mechanisms of transcriptional regulation by leukemia fusion proteins. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2021 Apr 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980.

Council of Science Editors:

Gow, Chien-Hung MD. Novel mechanisms of transcriptional regulation by leukemia fusion proteins. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980


NSYSU

15. Chan, Yu-Lin. Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-1β.

Degree: Master, Biological Sciences, 2012, NSYSU

 Grouper (Epinephelus coioides) is one of the important farmed fish in the southern Taiwan. However, grouper aquaculture in Taiwan has a serious problem of infection,… (more)

Subjects/Keywords: antiserum; lipopolysarcharide; fusion protein; IL -1β; Epinephelus coioides

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APA (6th Edition):

Chan, Y. (2012). Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-1β. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1113112-160654

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):

Chan, Yu-Lin. “Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-1β.” 2012. Thesis, NSYSU. Accessed April 18, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1113112-160654.

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

MLA Handbook (7th Edition):

Chan, Yu-Lin. “Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-1β.” 2012. Web. 18 Apr 2021.

Vancouver:

Chan Y. Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-1β. [Internet] [Thesis]. NSYSU; 2012. [cited 2021 Apr 18]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1113112-160654.

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

Council of Science Editors:

Chan Y. Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-Production and characterization of polyclonal antibody against Epinephelus coioides interleukin-1β. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1113112-160654

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


NSYSU

16. Chang, Shuo-Fu. Production and characterization of polyclonal antibody against Epinephelus coioides retinoic acid inducible gene-I.

Degree: Master, Biological Sciences, 2013, NSYSU

 Orange-spotted Grouper (Epinephelus coioides) is one of the important economically farmed fish in Taiwan. However, grouper aquaculture in Taiwan has a serious problem of infection,… (more)

Subjects/Keywords: Epinephelus coioides; RIG-I; poly(I:C); antiserum; fusion protein

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APA (6th Edition):

Chang, S. (2013). Production and characterization of polyclonal antibody against Epinephelus coioides retinoic acid inducible gene-I. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0327113-142030

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):

Chang, Shuo-Fu. “Production and characterization of polyclonal antibody against Epinephelus coioides retinoic acid inducible gene-I.” 2013. Thesis, NSYSU. Accessed April 18, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0327113-142030.

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

MLA Handbook (7th Edition):

Chang, Shuo-Fu. “Production and characterization of polyclonal antibody against Epinephelus coioides retinoic acid inducible gene-I.” 2013. Web. 18 Apr 2021.

Vancouver:

Chang S. Production and characterization of polyclonal antibody against Epinephelus coioides retinoic acid inducible gene-I. [Internet] [Thesis]. NSYSU; 2013. [cited 2021 Apr 18]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0327113-142030.

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

Council of Science Editors:

Chang S. Production and characterization of polyclonal antibody against Epinephelus coioides retinoic acid inducible gene-I. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0327113-142030

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

17. 小寺, 隆三. Manipulation of anabolic and catabolic responses with bone morphogenetic protein and zoledronic acid in a rat spinal fusion model.

Degree: 博士(医学), 2016, Oita University / 大分大学

 Bone fusion involves a complex set of regulated signaling pathways that control the formation of new bone matrix and the resorption of damaged bonematrix at… (more)

Subjects/Keywords: Bone morphogenetic protein; Zoledronic acid; Spine fusion; Rat model

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APA (6th Edition):

小寺, . (2016). Manipulation of anabolic and catabolic responses with bone morphogenetic protein and zoledronic acid in a rat spinal fusion model. (Thesis). Oita University / 大分大学. Retrieved from http://hdl.handle.net/10559/15609

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):

小寺, 隆三. “Manipulation of anabolic and catabolic responses with bone morphogenetic protein and zoledronic acid in a rat spinal fusion model.” 2016. Thesis, Oita University / 大分大学. Accessed April 18, 2021. http://hdl.handle.net/10559/15609.

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

MLA Handbook (7th Edition):

小寺, 隆三. “Manipulation of anabolic and catabolic responses with bone morphogenetic protein and zoledronic acid in a rat spinal fusion model.” 2016. Web. 18 Apr 2021.

Vancouver:

小寺 . Manipulation of anabolic and catabolic responses with bone morphogenetic protein and zoledronic acid in a rat spinal fusion model. [Internet] [Thesis]. Oita University / 大分大学; 2016. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10559/15609.

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

Council of Science Editors:

小寺 . Manipulation of anabolic and catabolic responses with bone morphogenetic protein and zoledronic acid in a rat spinal fusion model. [Thesis]. Oita University / 大分大学; 2016. Available from: http://hdl.handle.net/10559/15609

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


University of California – San Diego

18. Nelson, Katelyn. Functional Characterization of Oncogenic Driver FGFR3-TACC3.

Degree: Chemistry, 2018, University of California – San Diego

 Fibroblast Growth Factor Receptors (FGFRs) are critical for cell proliferation and differentiation. Mutation and/or translocation of FGFRs lead to aberrant signaling that often results in… (more)

Subjects/Keywords: Biochemistry; Cellular biology; cancer; FGFR; fusion protein; TACC; translocation

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APA (6th Edition):

Nelson, K. (2018). Functional Characterization of Oncogenic Driver FGFR3-TACC3. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9tj8f2k3

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):

Nelson, Katelyn. “Functional Characterization of Oncogenic Driver FGFR3-TACC3.” 2018. Thesis, University of California – San Diego. Accessed April 18, 2021. http://www.escholarship.org/uc/item/9tj8f2k3.

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

MLA Handbook (7th Edition):

Nelson, Katelyn. “Functional Characterization of Oncogenic Driver FGFR3-TACC3.” 2018. Web. 18 Apr 2021.

Vancouver:

Nelson K. Functional Characterization of Oncogenic Driver FGFR3-TACC3. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/9tj8f2k3.

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

Council of Science Editors:

Nelson K. Functional Characterization of Oncogenic Driver FGFR3-TACC3. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/9tj8f2k3

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


California State University – Northridge

19. Maly, Jan. Integral role of the SUMO fusion protein system in successful expression and purification of two difficult proteins for NMR studies.

Degree: MS, Chemistry and Biochemistry, 2013, California State University – Northridge

 Cellular signaling is one the hallmarks of multicellular organisms. The transmission of information between cells enables organisms to not only respond to their surrounding environment,… (more)

Subjects/Keywords: fusion protein; Dissertations, Academic  – CSUN  – Chemistry and Biochemistry  – Biochemistry.

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APA (6th Edition):

Maly, J. (2013). Integral role of the SUMO fusion protein system in successful expression and purification of two difficult proteins for NMR studies. (Masters Thesis). California State University – Northridge. Retrieved from http://hdl.handle.net/10211.2/3679

Chicago Manual of Style (16th Edition):

Maly, Jan. “Integral role of the SUMO fusion protein system in successful expression and purification of two difficult proteins for NMR studies.” 2013. Masters Thesis, California State University – Northridge. Accessed April 18, 2021. http://hdl.handle.net/10211.2/3679.

MLA Handbook (7th Edition):

Maly, Jan. “Integral role of the SUMO fusion protein system in successful expression and purification of two difficult proteins for NMR studies.” 2013. Web. 18 Apr 2021.

Vancouver:

Maly J. Integral role of the SUMO fusion protein system in successful expression and purification of two difficult proteins for NMR studies. [Internet] [Masters thesis]. California State University – Northridge; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10211.2/3679.

Council of Science Editors:

Maly J. Integral role of the SUMO fusion protein system in successful expression and purification of two difficult proteins for NMR studies. [Masters Thesis]. California State University – Northridge; 2013. Available from: http://hdl.handle.net/10211.2/3679


Northeastern University

20. Kates, Sydney. Design And Production Of A Fusion Protein For The Treatment Of Osteoarthritis.

Degree: MS, Department of Bioengineering, 2019, Northeastern University

 Osteoarthritis (OA) is a degenerative disease of the whole joint, affecting millions worldwide. Over time, the cartilage, synovium, and bone can degrade, leading to severe… (more)

Subjects/Keywords: Drug Delivery; Fusion Protein; Molecular Cloning; Osteoarthritis; Biomedical engineering

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APA (6th Edition):

Kates, S. (2019). Design And Production Of A Fusion Protein For The Treatment Of Osteoarthritis. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20317934

Chicago Manual of Style (16th Edition):

Kates, Sydney. “Design And Production Of A Fusion Protein For The Treatment Of Osteoarthritis.” 2019. Masters Thesis, Northeastern University. Accessed April 18, 2021. http://hdl.handle.net/2047/D20317934.

MLA Handbook (7th Edition):

Kates, Sydney. “Design And Production Of A Fusion Protein For The Treatment Of Osteoarthritis.” 2019. Web. 18 Apr 2021.

Vancouver:

Kates S. Design And Production Of A Fusion Protein For The Treatment Of Osteoarthritis. [Internet] [Masters thesis]. Northeastern University; 2019. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2047/D20317934.

Council of Science Editors:

Kates S. Design And Production Of A Fusion Protein For The Treatment Of Osteoarthritis. [Masters Thesis]. Northeastern University; 2019. Available from: http://hdl.handle.net/2047/D20317934


Colorado State University

21. Walker, Susanne N. Engineering and evolving helical proteins that improve in vivo stability and inhibit entry of Enfuvirtide-resistant HIV-1.

Degree: PhD, Chemistry, 2019, Colorado State University

 Methods for the stabilization of well-defined helical peptide drugs and basic research tools have received considerable attention in the last decade. Enfuvirtide is a 36-residue… (more)

Subjects/Keywords: HIV-1; protein engineering; membrane fusion; helix-grafting

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APA (6th Edition):

Walker, S. N. (2019). Engineering and evolving helical proteins that improve in vivo stability and inhibit entry of Enfuvirtide-resistant HIV-1. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/195296

Chicago Manual of Style (16th Edition):

Walker, Susanne N. “Engineering and evolving helical proteins that improve in vivo stability and inhibit entry of Enfuvirtide-resistant HIV-1.” 2019. Doctoral Dissertation, Colorado State University. Accessed April 18, 2021. http://hdl.handle.net/10217/195296.

MLA Handbook (7th Edition):

Walker, Susanne N. “Engineering and evolving helical proteins that improve in vivo stability and inhibit entry of Enfuvirtide-resistant HIV-1.” 2019. Web. 18 Apr 2021.

Vancouver:

Walker SN. Engineering and evolving helical proteins that improve in vivo stability and inhibit entry of Enfuvirtide-resistant HIV-1. [Internet] [Doctoral dissertation]. Colorado State University; 2019. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10217/195296.

Council of Science Editors:

Walker SN. Engineering and evolving helical proteins that improve in vivo stability and inhibit entry of Enfuvirtide-resistant HIV-1. [Doctoral Dissertation]. Colorado State University; 2019. Available from: http://hdl.handle.net/10217/195296


University of Adelaide

22. Charlton, Adam. Improved production of biopharmaceuticals by site-specific cleavage of fusion proteins expressed in Escherichia coli.

Degree: 2008, University of Adelaide

 The recombinant expression of heterologous proteins in microorganisms, such Escherichia coli, is often improved by producing the protein of interest translationally linked to another, often… (more)

Subjects/Keywords: biopharmaceuticals; fusion; protein; escherichia coli

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APA (6th Edition):

Charlton, A. (2008). Improved production of biopharmaceuticals by site-specific cleavage of fusion proteins expressed in Escherichia coli. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/59637

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):

Charlton, Adam. “Improved production of biopharmaceuticals by site-specific cleavage of fusion proteins expressed in Escherichia coli.” 2008. Thesis, University of Adelaide. Accessed April 18, 2021. http://hdl.handle.net/2440/59637.

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

MLA Handbook (7th Edition):

Charlton, Adam. “Improved production of biopharmaceuticals by site-specific cleavage of fusion proteins expressed in Escherichia coli.” 2008. Web. 18 Apr 2021.

Vancouver:

Charlton A. Improved production of biopharmaceuticals by site-specific cleavage of fusion proteins expressed in Escherichia coli. [Internet] [Thesis]. University of Adelaide; 2008. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2440/59637.

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

Council of Science Editors:

Charlton A. Improved production of biopharmaceuticals by site-specific cleavage of fusion proteins expressed in Escherichia coli. [Thesis]. University of Adelaide; 2008. Available from: http://hdl.handle.net/2440/59637

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


Australian National University

23. Porter, Joanne Loren. Improving enzyme properties through directed evolution .

Degree: 2015, Australian National University

 Enzymes are specific and economical biocatalysts and as such are highly desirable synthetic tools. While there are many examples of successful applications of enzymes into… (more)

Subjects/Keywords: enzyme; biocatalyst; synthetic; dienelactone hydrolase; engineering; protein; dihydrofolate; reductase; fusion

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APA (6th Edition):

Porter, J. L. (2015). Improving enzyme properties through directed evolution . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/110866

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):

Porter, Joanne Loren. “Improving enzyme properties through directed evolution .” 2015. Thesis, Australian National University. Accessed April 18, 2021. http://hdl.handle.net/1885/110866.

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

MLA Handbook (7th Edition):

Porter, Joanne Loren. “Improving enzyme properties through directed evolution .” 2015. Web. 18 Apr 2021.

Vancouver:

Porter JL. Improving enzyme properties through directed evolution . [Internet] [Thesis]. Australian National University; 2015. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1885/110866.

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

Council of Science Editors:

Porter JL. Improving enzyme properties through directed evolution . [Thesis]. Australian National University; 2015. Available from: http://hdl.handle.net/1885/110866

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


Princeton University

24. Baker, Richard Wayne. A direct for for SM proteins as templates for SNARE assembly .

Degree: PhD, 2015, Princeton University

 Intracellular membrane trafficking depends on the concerted action of soluble N-ethylmaleimide-sensitive factor attachment protein receptors (SNAREs) that physically drive membrane fusion. Membrane-bridging SNARE complexes are… (more)

Subjects/Keywords: HOPS complex; Membrane Fusion; Membrane Trafficking; SM protein; SNARE

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APA (6th Edition):

Baker, R. W. (2015). A direct for for SM proteins as templates for SNARE assembly . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp011v53k0363

Chicago Manual of Style (16th Edition):

Baker, Richard Wayne. “A direct for for SM proteins as templates for SNARE assembly .” 2015. Doctoral Dissertation, Princeton University. Accessed April 18, 2021. http://arks.princeton.edu/ark:/88435/dsp011v53k0363.

MLA Handbook (7th Edition):

Baker, Richard Wayne. “A direct for for SM proteins as templates for SNARE assembly .” 2015. Web. 18 Apr 2021.

Vancouver:

Baker RW. A direct for for SM proteins as templates for SNARE assembly . [Internet] [Doctoral dissertation]. Princeton University; 2015. [cited 2021 Apr 18]. Available from: http://arks.princeton.edu/ark:/88435/dsp011v53k0363.

Council of Science Editors:

Baker RW. A direct for for SM proteins as templates for SNARE assembly . [Doctoral Dissertation]. Princeton University; 2015. Available from: http://arks.princeton.edu/ark:/88435/dsp011v53k0363


University of Southern California

25. Wang, Yan. Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment.

Degree: PhD, Molecular Pharmacology and Toxicology, 2013, University of Southern California

 Long-acting insulin (INS) analogues that exhibit prolonged time-action profiles and liver-specificity are currently in great demand for diabetes treatment. Native INS and its protein precursor… (more)

Subjects/Keywords: transferrin; insulin; proinsulin; prodrug activation; recombinant fusion protein; diabetes

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APA (6th Edition):

Wang, Y. (2013). Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274

Chicago Manual of Style (16th Edition):

Wang, Yan. “Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment.” 2013. Doctoral Dissertation, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274.

MLA Handbook (7th Edition):

Wang, Yan. “Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment.” 2013. Web. 18 Apr 2021.

Vancouver:

Wang Y. Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274.

Council of Science Editors:

Wang Y. Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274


University of Southern California

26. Lee, Hsin-Fang. Preparation and characterization of Tf-G-CSF fusion protein.

Degree: MS, Molecular Pharmacology & Toxicology, 2008, University of Southern California

 In this study, Tf-H42-G-CSF fusion protein was engineered for investigating the effects of H4 helical linker 's on the fusion protein expression and the sequence… (more)

Subjects/Keywords: transferrin; G-CSF; fusion protein

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APA (6th Edition):

Lee, H. (2008). Preparation and characterization of Tf-G-CSF fusion protein. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189

Chicago Manual of Style (16th Edition):

Lee, Hsin-Fang. “Preparation and characterization of Tf-G-CSF fusion protein.” 2008. Masters Thesis, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189.

MLA Handbook (7th Edition):

Lee, Hsin-Fang. “Preparation and characterization of Tf-G-CSF fusion protein.” 2008. Web. 18 Apr 2021.

Vancouver:

Lee H. Preparation and characterization of Tf-G-CSF fusion protein. [Internet] [Masters thesis]. University of Southern California; 2008. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189.

Council of Science Editors:

Lee H. Preparation and characterization of Tf-G-CSF fusion protein. [Masters Thesis]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189

27. Schoeben, Melissa A. Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans.

Degree: MSin Biology, Biology, 2017, Missouri State University

  The acetic acid bacterium Gluconobacter oxydans is an industrially valuable microorganism, particularly in the production of acetic acid, D-gluconic acid, ketogluconic acids, dihydroxyacetone, and… (more)

Subjects/Keywords: Gluconobacter oxydans; fluorescent reporter; inducible promoter; fusion protein; genetic tools; Microbiology

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APA (6th Edition):

Schoeben, M. A. (2017). Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans. (Masters Thesis). Missouri State University. Retrieved from https://bearworks.missouristate.edu/theses/3117

Chicago Manual of Style (16th Edition):

Schoeben, Melissa A. “Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans.” 2017. Masters Thesis, Missouri State University. Accessed April 18, 2021. https://bearworks.missouristate.edu/theses/3117.

MLA Handbook (7th Edition):

Schoeben, Melissa A. “Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans.” 2017. Web. 18 Apr 2021.

Vancouver:

Schoeben MA. Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans. [Internet] [Masters thesis]. Missouri State University; 2017. [cited 2021 Apr 18]. Available from: https://bearworks.missouristate.edu/theses/3117.

Council of Science Editors:

Schoeben MA. Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans. [Masters Thesis]. Missouri State University; 2017. Available from: https://bearworks.missouristate.edu/theses/3117


The Ohio State University

28. Chaiwatpongsakorn, Supranee. Soluble Respiratory Syncytial Virus Fusion Protein in the Fully Cleaved, Pretriggered State, a Tool to Study Protein Triggering.

Degree: PhD, Comparative and Veterinary Medicine, 2011, The Ohio State University

 Respiratory syncytial virus (RSV), a member of the Paramyxoviridae family, Pneumovirinae subfamily is the most significant respiratory pathogen in infants and second only to influenza… (more)

Subjects/Keywords: Virology; RSV; fusion protein; triggering

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

APA (6th Edition):

Chaiwatpongsakorn, S. (2011). Soluble Respiratory Syncytial Virus Fusion Protein in the Fully Cleaved, Pretriggered State, a Tool to Study Protein Triggering. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1307730650

Chicago Manual of Style (16th Edition):

Chaiwatpongsakorn, Supranee. “Soluble Respiratory Syncytial Virus Fusion Protein in the Fully Cleaved, Pretriggered State, a Tool to Study Protein Triggering.” 2011. Doctoral Dissertation, The Ohio State University. Accessed April 18, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1307730650.

MLA Handbook (7th Edition):

Chaiwatpongsakorn, Supranee. “Soluble Respiratory Syncytial Virus Fusion Protein in the Fully Cleaved, Pretriggered State, a Tool to Study Protein Triggering.” 2011. Web. 18 Apr 2021.

Vancouver:

Chaiwatpongsakorn S. Soluble Respiratory Syncytial Virus Fusion Protein in the Fully Cleaved, Pretriggered State, a Tool to Study Protein Triggering. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2021 Apr 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1307730650.

Council of Science Editors:

Chaiwatpongsakorn S. Soluble Respiratory Syncytial Virus Fusion Protein in the Fully Cleaved, Pretriggered State, a Tool to Study Protein Triggering. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1307730650


University of Kentucky

29. Klimyte, Edita M. ELUCIDATING BINDING, FUSION AND ENTRY OF HUMAN METAPNEUMOVIRUS.

Degree: 2016, University of Kentucky

 Human metapneumovirus (HMPV) is a respiratory pathogen in the Paramyxoviridae family that infects nearly 100% of the world population. This enveloped RNA virus causes severe… (more)

Subjects/Keywords: Paramyxovirus; Human Metapneumovirus; Fusion Protein Membrane Fusion; Binding; Heparan Sulfate; Cystic Fibrosis; Other Immunology and Infectious Disease

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

APA (6th Edition):

Klimyte, E. M. (2016). ELUCIDATING BINDING, FUSION AND ENTRY OF HUMAN METAPNEUMOVIRUS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/biochem_etds/28

Chicago Manual of Style (16th Edition):

Klimyte, Edita M. “ELUCIDATING BINDING, FUSION AND ENTRY OF HUMAN METAPNEUMOVIRUS.” 2016. Doctoral Dissertation, University of Kentucky. Accessed April 18, 2021. https://uknowledge.uky.edu/biochem_etds/28.

MLA Handbook (7th Edition):

Klimyte, Edita M. “ELUCIDATING BINDING, FUSION AND ENTRY OF HUMAN METAPNEUMOVIRUS.” 2016. Web. 18 Apr 2021.

Vancouver:

Klimyte EM. ELUCIDATING BINDING, FUSION AND ENTRY OF HUMAN METAPNEUMOVIRUS. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2021 Apr 18]. Available from: https://uknowledge.uky.edu/biochem_etds/28.

Council of Science Editors:

Klimyte EM. ELUCIDATING BINDING, FUSION AND ENTRY OF HUMAN METAPNEUMOVIRUS. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/biochem_etds/28

30. 佐藤, 友人. 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.

Degree: 博士(バイオサイエンス), 2015, Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学

2014

Subjects/Keywords: Measles virus; Fusion protein; Membrane fusion; Refolding; Thermodynamic stability; Measles virus; Fusion protein; Membrane fusion; Refolding; Thermodynamic stability

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

APA (6th Edition):

佐藤, . (2015). 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. (Thesis). Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学. Retrieved from http://id.nii.ac.jp/1211/00000017/

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):

佐藤, 友人. “麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.” 2015. Thesis, Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学. Accessed April 18, 2021. http://id.nii.ac.jp/1211/00000017/.

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

MLA Handbook (7th Edition):

佐藤, 友人. “麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus.” 2015. Web. 18 Apr 2021.

Vancouver:

佐藤 . 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. [Internet] [Thesis]. Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学; 2015. [cited 2021 Apr 18]. Available from: http://id.nii.ac.jp/1211/00000017/.

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

Council of Science Editors:

佐藤 . 麻疹ウイルスF蛋白の膜融合活性発現の分子機構 : Molecular mechanism of expression of membranefusion activity by fusion protein of measles virus. [Thesis]. Nagahama Institute of Bio-Science and Technology / 長浜バイオ大学; 2015. Available from: http://id.nii.ac.jp/1211/00000017/

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

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