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You searched for +publisher:"Montana State University" +contributor:("Chairperson, Graduate Committee: Trevor Douglas"). Showing records 1 – 11 of 11 total matches.

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Montana State University

1. Allen, Mark Andrew. Protein cage architectures as a nano-platform for material synthesis and metal binding.

Degree: PhD, College of Letters & Science, 2006, Montana State University

 The metal binding affinity of certain viral protein cages allows the study of the role that metals play in such processes as viral assembly and… (more)

Subjects/Keywords: Proteins Structure.; Biosynthesis.; Ferritin.

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APA (6th Edition):

Allen, M. A. (2006). Protein cage architectures as a nano-platform for material synthesis and metal binding. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/815

Chicago Manual of Style (16th Edition):

Allen, Mark Andrew. “Protein cage architectures as a nano-platform for material synthesis and metal binding.” 2006. Doctoral Dissertation, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/815.

MLA Handbook (7th Edition):

Allen, Mark Andrew. “Protein cage architectures as a nano-platform for material synthesis and metal binding.” 2006. Web. 08 Aug 2020.

Vancouver:

Allen MA. Protein cage architectures as a nano-platform for material synthesis and metal binding. [Internet] [Doctoral dissertation]. Montana State University; 2006. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/815.

Council of Science Editors:

Allen MA. Protein cage architectures as a nano-platform for material synthesis and metal binding. [Doctoral Dissertation]. Montana State University; 2006. Available from: https://scholarworks.montana.edu/xmlui/handle/1/815


Montana State University

2. Edwards, Ethan James. The development of hybrid biomaterials using the virus-like particle (VLP) from bacteriophage P22.

Degree: College of Letters & Science, 2016, Montana State University

 A broad range of bio-composite materials have been developed through inspiration from biology. In particular, natural systems that confine, co-localize and protect their contents has… (more)

Subjects/Keywords: Biotechnology.; Bacteriophages.; Polymerization.; Catalysts.

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APA (6th Edition):

Edwards, E. J. (2016). The development of hybrid biomaterials using the virus-like particle (VLP) from bacteriophage P22. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/14318

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):

Edwards, Ethan James. “The development of hybrid biomaterials using the virus-like particle (VLP) from bacteriophage P22.” 2016. Thesis, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/14318.

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

MLA Handbook (7th Edition):

Edwards, Ethan James. “The development of hybrid biomaterials using the virus-like particle (VLP) from bacteriophage P22.” 2016. Web. 08 Aug 2020.

Vancouver:

Edwards EJ. The development of hybrid biomaterials using the virus-like particle (VLP) from bacteriophage P22. [Internet] [Thesis]. Montana State University; 2016. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/14318.

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

Council of Science Editors:

Edwards EJ. The development of hybrid biomaterials using the virus-like particle (VLP) from bacteriophage P22. [Thesis]. Montana State University; 2016. Available from: https://scholarworks.montana.edu/xmlui/handle/1/14318

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


Montana State University

3. Flenniken, Michelle Lynne. Protein cage architectures for targeted therapeutic and imaging agent delivery.

Degree: PhD, College of Letters & Science, 2006, Montana State University

 The advantages and disadvantages of all three architectures are described. Wild type and genetic variants of the Hsp, HFn, and CCMV cages were reacted for… (more)

Subjects/Keywords: Cowpea.; Plant diseases.; Proteins Structure.; Ferritin.; Nanotechnology.; Drug targeting.

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APA (6th Edition):

Flenniken, M. L. (2006). Protein cage architectures for targeted therapeutic and imaging agent delivery. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/1259

Chicago Manual of Style (16th Edition):

Flenniken, Michelle Lynne. “Protein cage architectures for targeted therapeutic and imaging agent delivery.” 2006. Doctoral Dissertation, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/1259.

MLA Handbook (7th Edition):

Flenniken, Michelle Lynne. “Protein cage architectures for targeted therapeutic and imaging agent delivery.” 2006. Web. 08 Aug 2020.

Vancouver:

Flenniken ML. Protein cage architectures for targeted therapeutic and imaging agent delivery. [Internet] [Doctoral dissertation]. Montana State University; 2006. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1259.

Council of Science Editors:

Flenniken ML. Protein cage architectures for targeted therapeutic and imaging agent delivery. [Doctoral Dissertation]. Montana State University; 2006. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1259


Montana State University

4. Johnson, Benjamin Lawrence. Monitoring protien cage nanopaticle morphology for applications in medicines and materials: Monitoring protein cage nanoparticle morphology for applications in medicines and materials.

Degree: MS, College of Letters & Science, 2011, Montana State University

 Protein cage nanoparticles are naturally occurring proteins found in all domains of life. The breadth of structural knowledge and the ability to modify protein cage… (more)

Subjects/Keywords: Bacteriophages.; Chromatographic analysis.; Lymphoid tissue.; Heat shock proteins.

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APA (6th Edition):

Johnson, B. L. (2011). Monitoring protien cage nanopaticle morphology for applications in medicines and materials: Monitoring protein cage nanoparticle morphology for applications in medicines and materials. (Masters Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/1569

Chicago Manual of Style (16th Edition):

Johnson, Benjamin Lawrence. “Monitoring protien cage nanopaticle morphology for applications in medicines and materials: Monitoring protein cage nanoparticle morphology for applications in medicines and materials.” 2011. Masters Thesis, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/1569.

MLA Handbook (7th Edition):

Johnson, Benjamin Lawrence. “Monitoring protien cage nanopaticle morphology for applications in medicines and materials: Monitoring protein cage nanoparticle morphology for applications in medicines and materials.” 2011. Web. 08 Aug 2020.

Vancouver:

Johnson BL. Monitoring protien cage nanopaticle morphology for applications in medicines and materials: Monitoring protein cage nanoparticle morphology for applications in medicines and materials. [Internet] [Masters thesis]. Montana State University; 2011. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1569.

Council of Science Editors:

Johnson BL. Monitoring protien cage nanopaticle morphology for applications in medicines and materials: Monitoring protein cage nanoparticle morphology for applications in medicines and materials. [Masters Thesis]. Montana State University; 2011. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1569

5. Jordan, Paul Campion. Biological redesign of virus particles for a new era of catalytic materials.

Degree: College of Letters & Science, 2016, Montana State University

 Biology has designed a suite of compartments and barriers that confine fundamental biochemical reactions. Such barriers include the membrane-bound organelles but also a suite of… (more)

Subjects/Keywords: Viruses.; Catalysis.; Bioengineering.; Hydrogenase.

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APA (6th Edition):

Jordan, P. C. (2016). Biological redesign of virus particles for a new era of catalytic materials. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/13800

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):

Jordan, Paul Campion. “Biological redesign of virus particles for a new era of catalytic materials.” 2016. Thesis, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/13800.

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

MLA Handbook (7th Edition):

Jordan, Paul Campion. “Biological redesign of virus particles for a new era of catalytic materials.” 2016. Web. 08 Aug 2020.

Vancouver:

Jordan PC. Biological redesign of virus particles for a new era of catalytic materials. [Internet] [Thesis]. Montana State University; 2016. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/13800.

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

Council of Science Editors:

Jordan PC. Biological redesign of virus particles for a new era of catalytic materials. [Thesis]. Montana State University; 2016. Available from: https://scholarworks.montana.edu/xmlui/handle/1/13800

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


Montana State University

6. Liepold, Lars Otto. Exploring the potential of protein cages as MRI contrast agents with an emphasis on protein cage characterization by mass spectrometry techniques.

Degree: PhD, College of Letters & Science, 2009, Montana State University

 Described here is the development of a protein cages as efficient and potentially relevant MRI contrast agents. Three approaches are outlined to fuse high affinity… (more)

Subjects/Keywords: Magnetic resonance imaging.; Contrast media (Diagnostic imaging); Gadolinium.; Mass spectrometry.; Ionization.

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APA (6th Edition):

Liepold, L. O. (2009). Exploring the potential of protein cages as MRI contrast agents with an emphasis on protein cage characterization by mass spectrometry techniques. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/1731

Chicago Manual of Style (16th Edition):

Liepold, Lars Otto. “Exploring the potential of protein cages as MRI contrast agents with an emphasis on protein cage characterization by mass spectrometry techniques.” 2009. Doctoral Dissertation, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/1731.

MLA Handbook (7th Edition):

Liepold, Lars Otto. “Exploring the potential of protein cages as MRI contrast agents with an emphasis on protein cage characterization by mass spectrometry techniques.” 2009. Web. 08 Aug 2020.

Vancouver:

Liepold LO. Exploring the potential of protein cages as MRI contrast agents with an emphasis on protein cage characterization by mass spectrometry techniques. [Internet] [Doctoral dissertation]. Montana State University; 2009. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1731.

Council of Science Editors:

Liepold LO. Exploring the potential of protein cages as MRI contrast agents with an emphasis on protein cage characterization by mass spectrometry techniques. [Doctoral Dissertation]. Montana State University; 2009. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1731

7. Lucon, Janice Elizabeth. Development of protein nanoparticle based composite materials.

Degree: PhD, College of Letters & Science, 2013, Montana State University

 Inspired by the core-shell composite structures found in nature, a range of protein based composites have been developed. These materials were made using synthetic approaches,… (more)

Subjects/Keywords: Proteins.; Nanoparticles.; Composite materials.

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APA (6th Edition):

Lucon, J. E. (2013). Development of protein nanoparticle based composite materials. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/1758

Chicago Manual of Style (16th Edition):

Lucon, Janice Elizabeth. “Development of protein nanoparticle based composite materials.” 2013. Doctoral Dissertation, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/1758.

MLA Handbook (7th Edition):

Lucon, Janice Elizabeth. “Development of protein nanoparticle based composite materials.” 2013. Web. 08 Aug 2020.

Vancouver:

Lucon JE. Development of protein nanoparticle based composite materials. [Internet] [Doctoral dissertation]. Montana State University; 2013. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1758.

Council of Science Editors:

Lucon JE. Development of protein nanoparticle based composite materials. [Doctoral Dissertation]. Montana State University; 2013. Available from: https://scholarworks.montana.edu/xmlui/handle/1/1758

8. O'Neil, Alison Linsley. Engineering bacteriophage P22 as a nanomaterial.

Degree: PhD, College of Letters & Science, 2013, Montana State University

 The precise architectures of viruses and virus-like particles are highly advantageous in synthetic materials applications. These nano-size compartments are perfectly suited to act as containers… (more)

Subjects/Keywords: Microencapsulation.; Nanostructured materials.; Bacteriophages.

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APA (6th Edition):

O'Neil, A. L. (2013). Engineering bacteriophage P22 as a nanomaterial. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/2740

Chicago Manual of Style (16th Edition):

O'Neil, Alison Linsley. “Engineering bacteriophage P22 as a nanomaterial.” 2013. Doctoral Dissertation, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/2740.

MLA Handbook (7th Edition):

O'Neil, Alison Linsley. “Engineering bacteriophage P22 as a nanomaterial.” 2013. Web. 08 Aug 2020.

Vancouver:

O'Neil AL. Engineering bacteriophage P22 as a nanomaterial. [Internet] [Doctoral dissertation]. Montana State University; 2013. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2740.

Council of Science Editors:

O'Neil AL. Engineering bacteriophage P22 as a nanomaterial. [Doctoral Dissertation]. Montana State University; 2013. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2740


Montana State University

9. Qazi, Shefah Alma. Designing virus-like nanoparticles as T 1-enhanced MRI contrast agents.

Degree: College of Letters & Science, 2014, Montana State University

 The field of nanotechnology is a rapidly growing field. In the past few decades, nanoparticles have been utilized for use in biomedical applications with a… (more)

Subjects/Keywords: Magnetic resonance imaging.; Nanoparticles.; Contrast media (Diagnostic imaging).; Gadolinium.

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APA (6th Edition):

Qazi, S. A. (2014). Designing virus-like nanoparticles as T 1-enhanced MRI contrast agents. (Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9418

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):

Qazi, Shefah Alma. “Designing virus-like nanoparticles as T 1-enhanced MRI contrast agents.” 2014. Thesis, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/9418.

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

MLA Handbook (7th Edition):

Qazi, Shefah Alma. “Designing virus-like nanoparticles as T 1-enhanced MRI contrast agents.” 2014. Web. 08 Aug 2020.

Vancouver:

Qazi SA. Designing virus-like nanoparticles as T 1-enhanced MRI contrast agents. [Internet] [Thesis]. Montana State University; 2014. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9418.

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

Council of Science Editors:

Qazi SA. Designing virus-like nanoparticles as T 1-enhanced MRI contrast agents. [Thesis]. Montana State University; 2014. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9418

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


Montana State University

10. Servid, Amy Eloise. Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.

Degree: PhD, College of Letters & Science, 2014, Montana State University

 In nature, protein cages are found within the structures of viruses, heat shock proteins, and ferritins. They assemble from subunits into spherical oligomeric structures, which… (more)

Subjects/Keywords: Protein engineering.; Nanomedicine.; Lungs.; Immunology.

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APA (6th Edition):

Servid, A. E. (2014). Characterization and embellishment of protein cages for nanomedical and nanomaterial applications. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/9137

Chicago Manual of Style (16th Edition):

Servid, Amy Eloise. “Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.” 2014. Doctoral Dissertation, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/9137.

MLA Handbook (7th Edition):

Servid, Amy Eloise. “Characterization and embellishment of protein cages for nanomedical and nanomaterial applications.” 2014. Web. 08 Aug 2020.

Vancouver:

Servid AE. Characterization and embellishment of protein cages for nanomedical and nanomaterial applications. [Internet] [Doctoral dissertation]. Montana State University; 2014. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9137.

Council of Science Editors:

Servid AE. Characterization and embellishment of protein cages for nanomedical and nanomaterial applications. [Doctoral Dissertation]. Montana State University; 2014. Available from: https://scholarworks.montana.edu/xmlui/handle/1/9137


Montana State University

11. Varpness, Zachary Bradley. Biomimetic synthesis of catalytic materials.

Degree: PhD, College of Letters & Science, 2007, Montana State University

 Fn was also used as the platform for the synthesis of catalytic platinum alloys of zinc and nickel. The alloys synthesized in this method showed… (more)

Subjects/Keywords: Catalysts.; Biomimetics.

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APA (6th Edition):

Varpness, Z. B. (2007). Biomimetic synthesis of catalytic materials. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/2471

Chicago Manual of Style (16th Edition):

Varpness, Zachary Bradley. “Biomimetic synthesis of catalytic materials.” 2007. Doctoral Dissertation, Montana State University. Accessed August 08, 2020. https://scholarworks.montana.edu/xmlui/handle/1/2471.

MLA Handbook (7th Edition):

Varpness, Zachary Bradley. “Biomimetic synthesis of catalytic materials.” 2007. Web. 08 Aug 2020.

Vancouver:

Varpness ZB. Biomimetic synthesis of catalytic materials. [Internet] [Doctoral dissertation]. Montana State University; 2007. [cited 2020 Aug 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2471.

Council of Science Editors:

Varpness ZB. Biomimetic synthesis of catalytic materials. [Doctoral Dissertation]. Montana State University; 2007. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2471

.