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Dept: Biochemistry  Level: doctoral

You searched for subject:( GTPase Activating Proteins metabolism 60). Showing records 1 – 30 of 88 total matches.

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University of Texas – Austin

1. -1281-6907. Developing synthetic, minimal promoters in Saccharomyces cerevisiae.

Degree: PhD, Biochemistry, 2019, University of Texas – Austin

 Promoters enable synthetic biologists to manipulate protein expression at the DNA level. For this reason, promoters are essential for almost all applications aiming to engineer… (more)

Subjects/Keywords: Promoters; Yeast; Saccharomyces cerevisiae; Synthetic biology; Upstream activating sequences; Core promoters

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APA (6th Edition):

-1281-6907. (2019). Developing synthetic, minimal promoters in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2216

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-1281-6907. “Developing synthetic, minimal promoters in Saccharomyces cerevisiae.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed December 15, 2019. http://dx.doi.org/10.26153/tsw/2216.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-1281-6907. “Developing synthetic, minimal promoters in Saccharomyces cerevisiae.” 2019. Web. 15 Dec 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-1281-6907. Developing synthetic, minimal promoters in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Dec 15]. Available from: http://dx.doi.org/10.26153/tsw/2216.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-1281-6907. Developing synthetic, minimal promoters in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2216

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

2. Bifano, Abby Lynn Shumaker. The Role of a Nuclear-Encoded DEAD-box Protein from <i>Saccharomyces</i> <i>cerevisiae</i> in Mitochondrial Group I Intron Splicing.

Degree: PhD, Biochemistry, 2010, Case Western Reserve University

  DEAD-box proteins are a large class of ATPases that are involved in almost all aspects of RNA metabolism. Many of these enzymes have been… (more)

Subjects/Keywords: Biochemistry; Molecular Biology; DEAD-box proteins; group I intron splicing; catalytic RNAs; mitochondrial RNA processing; <; i>; Saccharomyces<; /i>; <; i>; cerevisiae<; /i>

…vitro Activities of Mss116p Mutant Proteins ….… 99 Discussion… …122 Recombinant proteins and ATPase assays ….... 123 vi Crystal structure modeling… …and rates of duplex unwinding …..60 Table 3.1. Kinetic parameters for ATP… …121 Table 4.1. Summary of yeast mitochondrial introns and the proteins required for… …interactions in “closed” conformation of Mss116p and additional DEAD-box proteins .... 86 Figure 3.2… 

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APA (6th Edition):

Bifano, A. L. S. (2010). The Role of a Nuclear-Encoded DEAD-box Protein from <i>Saccharomyces</i> <i>cerevisiae</i> in Mitochondrial Group I Intron Splicing. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1283302534

Chicago Manual of Style (16th Edition):

Bifano, Abby Lynn Shumaker. “The Role of a Nuclear-Encoded DEAD-box Protein from <i>Saccharomyces</i> <i>cerevisiae</i> in Mitochondrial Group I Intron Splicing.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed December 15, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1283302534.

MLA Handbook (7th Edition):

Bifano, Abby Lynn Shumaker. “The Role of a Nuclear-Encoded DEAD-box Protein from <i>Saccharomyces</i> <i>cerevisiae</i> in Mitochondrial Group I Intron Splicing.” 2010. Web. 15 Dec 2019.

Vancouver:

Bifano ALS. The Role of a Nuclear-Encoded DEAD-box Protein from <i>Saccharomyces</i> <i>cerevisiae</i> in Mitochondrial Group I Intron Splicing. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2019 Dec 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1283302534.

Council of Science Editors:

Bifano ALS. The Role of a Nuclear-Encoded DEAD-box Protein from <i>Saccharomyces</i> <i>cerevisiae</i> in Mitochondrial Group I Intron Splicing. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1283302534


The Ohio State University

3. Pereira, Ryan Apolinario. FUNCTIONAL ANALYSIS OF TWO CONSERVED REGIONS OF ESCHERICHIA COLI ELONGATION FACTOR G AS STUDIED BY SITE-DIRECTED MUTAGENESIS.

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

 Elongation factor G (EF-G) catalyzes the translocation step of protein biosynthesis. The function of two conserved regions of E. coli EF-G, that are located at… (more)

Subjects/Keywords: PROTEIN SYNTHESIS; EF-G; GTPase; translation

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APA (6th Edition):

Pereira, R. A. (2002). FUNCTIONAL ANALYSIS OF TWO CONSERVED REGIONS OF ESCHERICHIA COLI ELONGATION FACTOR G AS STUDIED BY SITE-DIRECTED MUTAGENESIS. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1039030876

Chicago Manual of Style (16th Edition):

Pereira, Ryan Apolinario. “FUNCTIONAL ANALYSIS OF TWO CONSERVED REGIONS OF ESCHERICHIA COLI ELONGATION FACTOR G AS STUDIED BY SITE-DIRECTED MUTAGENESIS.” 2002. Doctoral Dissertation, The Ohio State University. Accessed December 15, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1039030876.

MLA Handbook (7th Edition):

Pereira, Ryan Apolinario. “FUNCTIONAL ANALYSIS OF TWO CONSERVED REGIONS OF ESCHERICHIA COLI ELONGATION FACTOR G AS STUDIED BY SITE-DIRECTED MUTAGENESIS.” 2002. Web. 15 Dec 2019.

Vancouver:

Pereira RA. FUNCTIONAL ANALYSIS OF TWO CONSERVED REGIONS OF ESCHERICHIA COLI ELONGATION FACTOR G AS STUDIED BY SITE-DIRECTED MUTAGENESIS. [Internet] [Doctoral dissertation]. The Ohio State University; 2002. [cited 2019 Dec 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039030876.

Council of Science Editors:

Pereira RA. FUNCTIONAL ANALYSIS OF TWO CONSERVED REGIONS OF ESCHERICHIA COLI ELONGATION FACTOR G AS STUDIED BY SITE-DIRECTED MUTAGENESIS. [Doctoral Dissertation]. The Ohio State University; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039030876


University of Texas – Austin

4. -1082-7768. Characterization of the Vibrio cholerae ferrous iron transport system, feo.

Degree: PhD, Biochemistry, 2015, University of Texas – Austin

 Feo is the major ferrous iron transport system in prokaryotes and has only been partially characterized, as its assembly and mechanism of transport have not… (more)

Subjects/Keywords: Iron; Vibrio cholerae; Transport metal; Protein cross-linking; Protein complex; Oligomerization; Membrane protein; GTPase; Mutagenesis

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APA (6th Edition):

-1082-7768. (2015). Characterization of the Vibrio cholerae ferrous iron transport system, feo. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63894

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-1082-7768. “Characterization of the Vibrio cholerae ferrous iron transport system, feo.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed December 15, 2019. http://hdl.handle.net/2152/63894.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-1082-7768. “Characterization of the Vibrio cholerae ferrous iron transport system, feo.” 2015. Web. 15 Dec 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-1082-7768. Characterization of the Vibrio cholerae ferrous iron transport system, feo. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2152/63894.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-1082-7768. Characterization of the Vibrio cholerae ferrous iron transport system, feo. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/63894

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of KwaZulu-Natal

5. Choveaux, David L. Recombinant expression and initial characterisation of two Plasmodium copper binding proteins.

Degree: PhD, Biochemistry, 2013, University of KwaZulu-Natal

 Plasmodium falciparum is a protozoan parasite responsible for the most severe form of human malaria, with infection often resulting in death. Efforts to control malaria… (more)

Subjects/Keywords: Biochemistry.; Copper proteins.

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APA (6th Edition):

Choveaux, D. L. (2013). Recombinant expression and initial characterisation of two Plasmodium copper binding proteins. (Doctoral Dissertation). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/10176

Chicago Manual of Style (16th Edition):

Choveaux, David L. “Recombinant expression and initial characterisation of two Plasmodium copper binding proteins.” 2013. Doctoral Dissertation, University of KwaZulu-Natal. Accessed December 15, 2019. http://hdl.handle.net/10413/10176.

MLA Handbook (7th Edition):

Choveaux, David L. “Recombinant expression and initial characterisation of two Plasmodium copper binding proteins.” 2013. Web. 15 Dec 2019.

Vancouver:

Choveaux DL. Recombinant expression and initial characterisation of two Plasmodium copper binding proteins. [Internet] [Doctoral dissertation]. University of KwaZulu-Natal; 2013. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10413/10176.

Council of Science Editors:

Choveaux DL. Recombinant expression and initial characterisation of two Plasmodium copper binding proteins. [Doctoral Dissertation]. University of KwaZulu-Natal; 2013. Available from: http://hdl.handle.net/10413/10176


Virginia Tech

6. Dahche, Hanan Mohamad. Dual-specific protein phosphatases in the &#60;i>Archaea&#60;/i>.

Degree: PhD, Biochemistry, 2010, Virginia Tech

 Three distinct families of PTPs, the conventional (cPTPs), low molecular weight (LMW PTPs), and Cdc25 PTPs, have converged upon a common catalytic mechanism and active… (more)

Subjects/Keywords: dual-specific phosphatase; <; i>; Archaea<; /i>;

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APA (6th Edition):

Dahche, H. M. (2010). Dual-specific protein phosphatases in the <i>Archaea</i>. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/37625

Chicago Manual of Style (16th Edition):

Dahche, Hanan Mohamad. “Dual-specific protein phosphatases in the <i>Archaea</i>.” 2010. Doctoral Dissertation, Virginia Tech. Accessed December 15, 2019. http://hdl.handle.net/10919/37625.

MLA Handbook (7th Edition):

Dahche, Hanan Mohamad. “Dual-specific protein phosphatases in the <i>Archaea</i>.” 2010. Web. 15 Dec 2019.

Vancouver:

Dahche HM. Dual-specific protein phosphatases in the <i>Archaea</i>. [Internet] [Doctoral dissertation]. Virginia Tech; 2010. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10919/37625.

Council of Science Editors:

Dahche HM. Dual-specific protein phosphatases in the <i>Archaea</i>. [Doctoral Dissertation]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/37625


University of Iowa

7. Oonthonpan, Lalita. Two human Mitochondrial Pyruvate Carrier mutations reveal distinct mechanisms of molecular pathogenesis.

Degree: PhD, Biochemistry, 2019, University of Iowa

  The Mitochondrial Pyruvate Carrier (MPC) occupies a central metabolic node by transporting cytosolic pyruvate into the mitochondrial matrix, thereby linking glycolysis with mitochondrial metabolism.… (more)

Subjects/Keywords: Carbohydrate metabolism; Cell Biology; Inborn error; Metabolism; Mitochondria; Transport; Biochemistry

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APA (6th Edition):

Oonthonpan, L. (2019). Two human Mitochondrial Pyruvate Carrier mutations reveal distinct mechanisms of molecular pathogenesis. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/7006

Chicago Manual of Style (16th Edition):

Oonthonpan, Lalita. “Two human Mitochondrial Pyruvate Carrier mutations reveal distinct mechanisms of molecular pathogenesis.” 2019. Doctoral Dissertation, University of Iowa. Accessed December 15, 2019. https://ir.uiowa.edu/etd/7006.

MLA Handbook (7th Edition):

Oonthonpan, Lalita. “Two human Mitochondrial Pyruvate Carrier mutations reveal distinct mechanisms of molecular pathogenesis.” 2019. Web. 15 Dec 2019.

Vancouver:

Oonthonpan L. Two human Mitochondrial Pyruvate Carrier mutations reveal distinct mechanisms of molecular pathogenesis. [Internet] [Doctoral dissertation]. University of Iowa; 2019. [cited 2019 Dec 15]. Available from: https://ir.uiowa.edu/etd/7006.

Council of Science Editors:

Oonthonpan L. Two human Mitochondrial Pyruvate Carrier mutations reveal distinct mechanisms of molecular pathogenesis. [Doctoral Dissertation]. University of Iowa; 2019. Available from: https://ir.uiowa.edu/etd/7006


North Carolina State University

8. Buhrman, Gregory Kale. Application of the Multiple Solvent Crystal Structures Method to Analyze the Protein Binding Surface of H-Ras Protein.

Degree: PhD, Biochemistry, 2006, North Carolina State University

 H-Ras is a member of the small, monomeric GTPase protein superfamily. H-Ras functions as a 'molecular switch', using nucleotide dependent conformational changes to relay signals… (more)

Subjects/Keywords: protein structure; Ras; GTPase; organic solvents; MSCS; x-ray crystallography; protein binding sites

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APA (6th Edition):

Buhrman, G. K. (2006). Application of the Multiple Solvent Crystal Structures Method to Analyze the Protein Binding Surface of H-Ras Protein. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5664

Chicago Manual of Style (16th Edition):

Buhrman, Gregory Kale. “Application of the Multiple Solvent Crystal Structures Method to Analyze the Protein Binding Surface of H-Ras Protein.” 2006. Doctoral Dissertation, North Carolina State University. Accessed December 15, 2019. http://www.lib.ncsu.edu/resolver/1840.16/5664.

MLA Handbook (7th Edition):

Buhrman, Gregory Kale. “Application of the Multiple Solvent Crystal Structures Method to Analyze the Protein Binding Surface of H-Ras Protein.” 2006. Web. 15 Dec 2019.

Vancouver:

Buhrman GK. Application of the Multiple Solvent Crystal Structures Method to Analyze the Protein Binding Surface of H-Ras Protein. [Internet] [Doctoral dissertation]. North Carolina State University; 2006. [cited 2019 Dec 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5664.

Council of Science Editors:

Buhrman GK. Application of the Multiple Solvent Crystal Structures Method to Analyze the Protein Binding Surface of H-Ras Protein. [Doctoral Dissertation]. North Carolina State University; 2006. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5664


University of Texas – Austin

9. Sadow, Jennifer Beth Hurley. The x-ray crystal structure of wheat translation initiation factor eIF4E.

Degree: PhD, Biochemistry, 2002, University of Texas – Austin

Subjects/Keywords: Proteins – Synthesis; Proteins – Structure; Crystallography

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APA (6th Edition):

Sadow, J. B. H. (2002). The x-ray crystal structure of wheat translation initiation factor eIF4E. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/895

Chicago Manual of Style (16th Edition):

Sadow, Jennifer Beth Hurley. “The x-ray crystal structure of wheat translation initiation factor eIF4E.” 2002. Doctoral Dissertation, University of Texas – Austin. Accessed December 15, 2019. http://hdl.handle.net/2152/895.

MLA Handbook (7th Edition):

Sadow, Jennifer Beth Hurley. “The x-ray crystal structure of wheat translation initiation factor eIF4E.” 2002. Web. 15 Dec 2019.

Vancouver:

Sadow JBH. The x-ray crystal structure of wheat translation initiation factor eIF4E. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2002. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2152/895.

Council of Science Editors:

Sadow JBH. The x-ray crystal structure of wheat translation initiation factor eIF4E. [Doctoral Dissertation]. University of Texas – Austin; 2002. Available from: http://hdl.handle.net/2152/895


Virginia Tech

10. Peterson, Tina Marie Loane. &#60;i>Plasmodium&#60;/i>-Induced Nitrosative Stress in &#60;i>Anopheles stephensi&#60;/i>: The Cost of Host Defense.

Degree: PhD, Biochemistry, 2005, Virginia Tech

 Both vertebrates and anopheline mosquitoes inhibit &#60;i>Plasmodium&#60;/i> spp. (malaria parasite) development via induction of nitric oxide (â ¢NO) synthase. Expression of &#60;i>Anopheles stephensi&#60;/i> â ¢NO… (more)

Subjects/Keywords: malaria; nitric oxide; <; i>; Anopheles<; /i>;

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APA (6th Edition):

Peterson, T. M. L. (2005). <i>Plasmodium</i>-Induced Nitrosative Stress in <i>Anopheles stephensi</i>: The Cost of Host Defense. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/27943

Chicago Manual of Style (16th Edition):

Peterson, Tina Marie Loane. “<i>Plasmodium</i>-Induced Nitrosative Stress in <i>Anopheles stephensi</i>: The Cost of Host Defense.” 2005. Doctoral Dissertation, Virginia Tech. Accessed December 15, 2019. http://hdl.handle.net/10919/27943.

MLA Handbook (7th Edition):

Peterson, Tina Marie Loane. “<i>Plasmodium</i>-Induced Nitrosative Stress in <i>Anopheles stephensi</i>: The Cost of Host Defense.” 2005. Web. 15 Dec 2019.

Vancouver:

Peterson TML. <i>Plasmodium</i>-Induced Nitrosative Stress in <i>Anopheles stephensi</i>: The Cost of Host Defense. [Internet] [Doctoral dissertation]. Virginia Tech; 2005. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10919/27943.

Council of Science Editors:

Peterson TML. <i>Plasmodium</i>-Induced Nitrosative Stress in <i>Anopheles stephensi</i>: The Cost of Host Defense. [Doctoral Dissertation]. Virginia Tech; 2005. Available from: http://hdl.handle.net/10919/27943


Massey University

11. Stowell, Allan Robert. Acetaldehyde metabolism in mammals.

Degree: PhD, Biochemistry, 1977, Massey University

 To determine the pharmacological importance of acetaldehyde in the actions of ethanol, this study was planned to define the levels of free acetaldehyde occurring in… (more)

Subjects/Keywords: Acetaldehyde; Metabolism; Mammals

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APA (6th Edition):

Stowell, A. R. (1977). Acetaldehyde metabolism in mammals. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/3667

Chicago Manual of Style (16th Edition):

Stowell, Allan Robert. “Acetaldehyde metabolism in mammals.” 1977. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/3667.

MLA Handbook (7th Edition):

Stowell, Allan Robert. “Acetaldehyde metabolism in mammals.” 1977. Web. 15 Dec 2019.

Vancouver:

Stowell AR. Acetaldehyde metabolism in mammals. [Internet] [Doctoral dissertation]. Massey University; 1977. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/3667.

Council of Science Editors:

Stowell AR. Acetaldehyde metabolism in mammals. [Doctoral Dissertation]. Massey University; 1977. Available from: http://hdl.handle.net/10179/3667


University of Iowa

12. Cushing, Emily Malcolm. Regulation of plasma triglycerides by ANGPTL4 and GPIHBP1.

Degree: PhD, Biochemistry, 2018, University of Iowa

  The absorption, packaging, and delivery of fat to appropriate peripheral tissues is essential for maintaining metabolic homeostasis, and defects or dysregulation of these processes… (more)

Subjects/Keywords: ANGPTL4; chylomicron; GPIHBP1; LPL; metabolism; triglycerides; Biochemistry

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APA (6th Edition):

Cushing, E. M. (2018). Regulation of plasma triglycerides by ANGPTL4 and GPIHBP1. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6399

Chicago Manual of Style (16th Edition):

Cushing, Emily Malcolm. “Regulation of plasma triglycerides by ANGPTL4 and GPIHBP1.” 2018. Doctoral Dissertation, University of Iowa. Accessed December 15, 2019. https://ir.uiowa.edu/etd/6399.

MLA Handbook (7th Edition):

Cushing, Emily Malcolm. “Regulation of plasma triglycerides by ANGPTL4 and GPIHBP1.” 2018. Web. 15 Dec 2019.

Vancouver:

Cushing EM. Regulation of plasma triglycerides by ANGPTL4 and GPIHBP1. [Internet] [Doctoral dissertation]. University of Iowa; 2018. [cited 2019 Dec 15]. Available from: https://ir.uiowa.edu/etd/6399.

Council of Science Editors:

Cushing EM. Regulation of plasma triglycerides by ANGPTL4 and GPIHBP1. [Doctoral Dissertation]. University of Iowa; 2018. Available from: https://ir.uiowa.edu/etd/6399


North Carolina State University

13. Lieberman, David. Comparison of the Catalytic Activities of Ricin A-Chain, Maize rproRIP1, MaizeRIP1, and Two Maize rproRIP1 Deletion Mutants Interacting with an RNA 10-mer GAGA Tetraloop.

Degree: PhD, Biochemistry, 2003, North Carolina State University

 Ribosome-inactivating proteins (RIPs) catalytically depurinate a conserved adenine in the ribosomal alpha-sarcin domain, and it is believed that the local structure surrounding the target adenine… (more)

Subjects/Keywords: Ribosome-inactivating proteins

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APA (6th Edition):

Lieberman, D. (2003). Comparison of the Catalytic Activities of Ricin A-Chain, Maize rproRIP1, MaizeRIP1, and Two Maize rproRIP1 Deletion Mutants Interacting with an RNA 10-mer GAGA Tetraloop. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4665

Chicago Manual of Style (16th Edition):

Lieberman, David. “Comparison of the Catalytic Activities of Ricin A-Chain, Maize rproRIP1, MaizeRIP1, and Two Maize rproRIP1 Deletion Mutants Interacting with an RNA 10-mer GAGA Tetraloop.” 2003. Doctoral Dissertation, North Carolina State University. Accessed December 15, 2019. http://www.lib.ncsu.edu/resolver/1840.16/4665.

MLA Handbook (7th Edition):

Lieberman, David. “Comparison of the Catalytic Activities of Ricin A-Chain, Maize rproRIP1, MaizeRIP1, and Two Maize rproRIP1 Deletion Mutants Interacting with an RNA 10-mer GAGA Tetraloop.” 2003. Web. 15 Dec 2019.

Vancouver:

Lieberman D. Comparison of the Catalytic Activities of Ricin A-Chain, Maize rproRIP1, MaizeRIP1, and Two Maize rproRIP1 Deletion Mutants Interacting with an RNA 10-mer GAGA Tetraloop. [Internet] [Doctoral dissertation]. North Carolina State University; 2003. [cited 2019 Dec 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4665.

Council of Science Editors:

Lieberman D. Comparison of the Catalytic Activities of Ricin A-Chain, Maize rproRIP1, MaizeRIP1, and Two Maize rproRIP1 Deletion Mutants Interacting with an RNA 10-mer GAGA Tetraloop. [Doctoral Dissertation]. North Carolina State University; 2003. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4665


North Carolina State University

14. Nelson, Steevenson. Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding.

Degree: PhD, Biochemistry, 2006, North Carolina State University

 Sindbis virus particles are composed of three structural proteins (C/E2/E1). The E1 glycoprotein is organized into a highly constrained, energy-rich conformation. Its hypothesized that this… (more)

Subjects/Keywords: Furin; proteins; truncated

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APA (6th Edition):

Nelson, S. (2006). Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5050

Chicago Manual of Style (16th Edition):

Nelson, Steevenson. “Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding.” 2006. Doctoral Dissertation, North Carolina State University. Accessed December 15, 2019. http://www.lib.ncsu.edu/resolver/1840.16/5050.

MLA Handbook (7th Edition):

Nelson, Steevenson. “Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding.” 2006. Web. 15 Dec 2019.

Vancouver:

Nelson S. Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding. [Internet] [Doctoral dissertation]. North Carolina State University; 2006. [cited 2019 Dec 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5050.

Council of Science Editors:

Nelson S. Characterization of Furin Protease Sensitive Site Processing and Its Effects on Sindbis Virus Assembly and Budding. [Doctoral Dissertation]. North Carolina State University; 2006. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5050


North Carolina State University

15. Nicely, Nathan. Study of Protein Binding Sites on the GTPase RalA and the Sugar-binding Protein Hen Egg White Lysozyme.

Degree: PhD, Biochemistry, 2006, North Carolina State University

 Hen egg white lysozyme and simian RalA are two very different proteins by function and category. Lysozyme is an extracellular enzyme that catalyzes the hydrolysis… (more)

Subjects/Keywords: protein interfaces; organic solvents; crystallography; RalA; binding sites; protein binding sites; RalB; lysozyme; GTPase; Ral

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APA (6th Edition):

Nicely, N. (2006). Study of Protein Binding Sites on the GTPase RalA and the Sugar-binding Protein Hen Egg White Lysozyme. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4767

Chicago Manual of Style (16th Edition):

Nicely, Nathan. “Study of Protein Binding Sites on the GTPase RalA and the Sugar-binding Protein Hen Egg White Lysozyme.” 2006. Doctoral Dissertation, North Carolina State University. Accessed December 15, 2019. http://www.lib.ncsu.edu/resolver/1840.16/4767.

MLA Handbook (7th Edition):

Nicely, Nathan. “Study of Protein Binding Sites on the GTPase RalA and the Sugar-binding Protein Hen Egg White Lysozyme.” 2006. Web. 15 Dec 2019.

Vancouver:

Nicely N. Study of Protein Binding Sites on the GTPase RalA and the Sugar-binding Protein Hen Egg White Lysozyme. [Internet] [Doctoral dissertation]. North Carolina State University; 2006. [cited 2019 Dec 15]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4767.

Council of Science Editors:

Nicely N. Study of Protein Binding Sites on the GTPase RalA and the Sugar-binding Protein Hen Egg White Lysozyme. [Doctoral Dissertation]. North Carolina State University; 2006. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4767


Massey University

16. Jones, William Thomas. Studies on the foaming properties of proteins : the role of soluble leaf proteins and other surfactants in the persistence of bloat foams.

Degree: PhD, Biochemistry, 1971, Massey University

 Methods were developed for the isolation of the soluble leaf proteins in as pure a form as possible and free of any phenoloxidase products. This… (more)

Subjects/Keywords: Proteins; Soluble leaf proteins; Surfactants; Bloat foams

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APA (6th Edition):

Jones, W. T. (1971). Studies on the foaming properties of proteins : the role of soluble leaf proteins and other surfactants in the persistence of bloat foams. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/3285

Chicago Manual of Style (16th Edition):

Jones, William Thomas. “Studies on the foaming properties of proteins : the role of soluble leaf proteins and other surfactants in the persistence of bloat foams.” 1971. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/3285.

MLA Handbook (7th Edition):

Jones, William Thomas. “Studies on the foaming properties of proteins : the role of soluble leaf proteins and other surfactants in the persistence of bloat foams.” 1971. Web. 15 Dec 2019.

Vancouver:

Jones WT. Studies on the foaming properties of proteins : the role of soluble leaf proteins and other surfactants in the persistence of bloat foams. [Internet] [Doctoral dissertation]. Massey University; 1971. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/3285.

Council of Science Editors:

Jones WT. Studies on the foaming properties of proteins : the role of soluble leaf proteins and other surfactants in the persistence of bloat foams. [Doctoral Dissertation]. Massey University; 1971. Available from: http://hdl.handle.net/10179/3285


Virginia Commonwealth University

17. Griffiths, Rachael. The Regulation of Platelet Activating Factor Acetylhydrolase by Oxidized Phospholipids.

Degree: PhD, Biochemistry, 2009, Virginia Commonwealth University

 Platelet-activating factor acetylhydrolase (PAFAH) is elevated in atherosclerosis and may play a role in pathogenesis of this disease. Molecular mechanisms regulating the expression of this… (more)

Subjects/Keywords: Platelet activating factor acetylhydrolase; atherosclerosis; phospholipase a2; atherosclerosis; monocytes; macrophages; dendritic cells; oxidized phospholipids; periodontitis; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Griffiths, R. (2009). The Regulation of Platelet Activating Factor Acetylhydrolase by Oxidized Phospholipids. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1913

Chicago Manual of Style (16th Edition):

Griffiths, Rachael. “The Regulation of Platelet Activating Factor Acetylhydrolase by Oxidized Phospholipids.” 2009. Doctoral Dissertation, Virginia Commonwealth University. Accessed December 15, 2019. https://scholarscompass.vcu.edu/etd/1913.

MLA Handbook (7th Edition):

Griffiths, Rachael. “The Regulation of Platelet Activating Factor Acetylhydrolase by Oxidized Phospholipids.” 2009. Web. 15 Dec 2019.

Vancouver:

Griffiths R. The Regulation of Platelet Activating Factor Acetylhydrolase by Oxidized Phospholipids. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2009. [cited 2019 Dec 15]. Available from: https://scholarscompass.vcu.edu/etd/1913.

Council of Science Editors:

Griffiths R. The Regulation of Platelet Activating Factor Acetylhydrolase by Oxidized Phospholipids. [Doctoral Dissertation]. Virginia Commonwealth University; 2009. Available from: https://scholarscompass.vcu.edu/etd/1913


University of Utah

18. Cardon, Caleb Michael. PER-ARNT-SIM kinase regulates nutrient utilization and growth.

Degree: PhD, Biochemistry, 2011, University of Utah

 There is a fundamental connection between growth and nutrient availability. An inbalance between energy intake and energy expenditure can lead to the common diseases of… (more)

Subjects/Keywords: Growth; Kinase; Metabolism; Nutrient; PAS; TOR; PER-ARNT-SIM kinase; Bioenergetics

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APA (6th Edition):

Cardon, C. M. (2011). PER-ARNT-SIM kinase regulates nutrient utilization and growth. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/355/rec/1821

Chicago Manual of Style (16th Edition):

Cardon, Caleb Michael. “PER-ARNT-SIM kinase regulates nutrient utilization and growth.” 2011. Doctoral Dissertation, University of Utah. Accessed December 15, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/355/rec/1821.

MLA Handbook (7th Edition):

Cardon, Caleb Michael. “PER-ARNT-SIM kinase regulates nutrient utilization and growth.” 2011. Web. 15 Dec 2019.

Vancouver:

Cardon CM. PER-ARNT-SIM kinase regulates nutrient utilization and growth. [Internet] [Doctoral dissertation]. University of Utah; 2011. [cited 2019 Dec 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/355/rec/1821.

Council of Science Editors:

Cardon CM. PER-ARNT-SIM kinase regulates nutrient utilization and growth. [Doctoral Dissertation]. University of Utah; 2011. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/355/rec/1821


University of Pretoria

19. Smit, Salome. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria presents a global health risk that is becoming increasingly difficult to treat due to increased resistance of both the parasite and mosquito to all… (more)

Subjects/Keywords: Methionine metabolism; Malaria; S-adenosylmethionine decarboxylase; Mosquito; Parasite; UCTD

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APA (6th Edition):

Smit, S. (2011). Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/25743

Chicago Manual of Style (16th Edition):

Smit, Salome. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.” 2011. Doctoral Dissertation, University of Pretoria. Accessed December 15, 2019. http://hdl.handle.net/2263/25743.

MLA Handbook (7th Edition):

Smit, Salome. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.” 2011. Web. 15 Dec 2019.

Vancouver:

Smit S. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2263/25743.

Council of Science Editors:

Smit S. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/25743


Case Western Reserve University

20. Wexler, Isaiah David. Disorders of pyruvate metabolism.

Degree: PhD, Biochemistry, 1995, Case Western Reserve University

 Pyruvate, a three carbon a-keto acid, stands at the crossroads of intermediary metabolism. The products of pyruvate metabolism are involved in multiple metabolic processes including… (more)

Subjects/Keywords: Chemistry, Biochemistry; Pyruvate metabolism; disorders

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APA (6th Edition):

Wexler, I. D. (1995). Disorders of pyruvate metabolism. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1057937741

Chicago Manual of Style (16th Edition):

Wexler, Isaiah David. “Disorders of pyruvate metabolism.” 1995. Doctoral Dissertation, Case Western Reserve University. Accessed December 15, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1057937741.

MLA Handbook (7th Edition):

Wexler, Isaiah David. “Disorders of pyruvate metabolism.” 1995. Web. 15 Dec 2019.

Vancouver:

Wexler ID. Disorders of pyruvate metabolism. [Internet] [Doctoral dissertation]. Case Western Reserve University; 1995. [cited 2019 Dec 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1057937741.

Council of Science Editors:

Wexler ID. Disorders of pyruvate metabolism. [Doctoral Dissertation]. Case Western Reserve University; 1995. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1057937741


Massey University

21. Smart, John Beresford. The role of pyruvate kinase in the regulation of glycolysis and gluconeogenesis in Propionibacterium shermanii.

Degree: PhD, Biochemistry, 1980, Massey University

 Pyruvate kinase catalyses the main irreversible reaction of glycolysis in Propionbacterium shermanii since the ATP-dependent phosphofructokinase is largely replaced by a pyrophosphate-dependent phosphofructokinase catalysing a… (more)

Subjects/Keywords: Bacteria; Physiology; Pyruvates; Metabolism; Carbohydrates

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APA (6th Edition):

Smart, J. B. (1980). The role of pyruvate kinase in the regulation of glycolysis and gluconeogenesis in Propionibacterium shermanii. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/3535

Chicago Manual of Style (16th Edition):

Smart, John Beresford. “The role of pyruvate kinase in the regulation of glycolysis and gluconeogenesis in Propionibacterium shermanii.” 1980. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/3535.

MLA Handbook (7th Edition):

Smart, John Beresford. “The role of pyruvate kinase in the regulation of glycolysis and gluconeogenesis in Propionibacterium shermanii.” 1980. Web. 15 Dec 2019.

Vancouver:

Smart JB. The role of pyruvate kinase in the regulation of glycolysis and gluconeogenesis in Propionibacterium shermanii. [Internet] [Doctoral dissertation]. Massey University; 1980. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/3535.

Council of Science Editors:

Smart JB. The role of pyruvate kinase in the regulation of glycolysis and gluconeogenesis in Propionibacterium shermanii. [Doctoral Dissertation]. Massey University; 1980. Available from: http://hdl.handle.net/10179/3535


Massey University

22. McLean, John William. The intracellular site of synthesis of fructose 1,6-bisphosphatase in rat liver.

Degree: PhD, Biochemistry, 1979, Massey University

 Fructose-1,6-bisphosphatase (FBPase, E.C. 3.1.3.11) has been purified from rat liver cytoplasm by a new purification procedure. Monospecific antibodies were raised to FBPase in rabbits to… (more)

Subjects/Keywords: Rats; Metabolism; Fructose; Synthesis

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APA (6th Edition):

McLean, J. W. (1979). The intracellular site of synthesis of fructose 1,6-bisphosphatase in rat liver. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/3625

Chicago Manual of Style (16th Edition):

McLean, John William. “The intracellular site of synthesis of fructose 1,6-bisphosphatase in rat liver.” 1979. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/3625.

MLA Handbook (7th Edition):

McLean, John William. “The intracellular site of synthesis of fructose 1,6-bisphosphatase in rat liver.” 1979. Web. 15 Dec 2019.

Vancouver:

McLean JW. The intracellular site of synthesis of fructose 1,6-bisphosphatase in rat liver. [Internet] [Doctoral dissertation]. Massey University; 1979. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/3625.

Council of Science Editors:

McLean JW. The intracellular site of synthesis of fructose 1,6-bisphosphatase in rat liver. [Doctoral Dissertation]. Massey University; 1979. Available from: http://hdl.handle.net/10179/3625


Massey University

23. Ahn, Meekyung. Substrate analogues as mechanistic probes for 3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase and 3-Deoxy-D-manno-octulosonate 8-phosphate synthase.

Degree: PhD, Biochemistry, 2007, Massey University

 3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase (DAH7P synthase) catalyses the condensation reaction between phosphoenolpyrtivate (PEP) and the four-carbon monosaccharide D-erythrose 4-phosphate (D-E4P). 3-Deoxy-D-manno-octulosonate 8-phosphate synthase (KDO8P synthase) catalyses… (more)

Subjects/Keywords: Shikimic acid; Metabolism; Enzymes; Synthesis

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APA (6th Edition):

Ahn, M. (2007). Substrate analogues as mechanistic probes for 3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase and 3-Deoxy-D-manno-octulosonate 8-phosphate synthase. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/3873

Chicago Manual of Style (16th Edition):

Ahn, Meekyung. “Substrate analogues as mechanistic probes for 3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase and 3-Deoxy-D-manno-octulosonate 8-phosphate synthase.” 2007. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/3873.

MLA Handbook (7th Edition):

Ahn, Meekyung. “Substrate analogues as mechanistic probes for 3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase and 3-Deoxy-D-manno-octulosonate 8-phosphate synthase.” 2007. Web. 15 Dec 2019.

Vancouver:

Ahn M. Substrate analogues as mechanistic probes for 3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase and 3-Deoxy-D-manno-octulosonate 8-phosphate synthase. [Internet] [Doctoral dissertation]. Massey University; 2007. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/3873.

Council of Science Editors:

Ahn M. Substrate analogues as mechanistic probes for 3-Deoxy-D-arabino-heptulosonate 7-phosphate synthase and 3-Deoxy-D-manno-octulosonate 8-phosphate synthase. [Doctoral Dissertation]. Massey University; 2007. Available from: http://hdl.handle.net/10179/3873


Massey University

24. Robertson, John Gray. Endogenous metabolism of Nocardia corallina.

Degree: PhD, Biochemistry, 1968, Massey University

 The endogenous metabolism of the soil microorganism N. corallina has been studied with special reference to physiological and structural changes in starvation conditions. When N.… (more)

Subjects/Keywords: Nocardia corallina; Metabolism; Biochemistry

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APA (6th Edition):

Robertson, J. G. (1968). Endogenous metabolism of Nocardia corallina. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/2396

Chicago Manual of Style (16th Edition):

Robertson, John Gray. “Endogenous metabolism of Nocardia corallina.” 1968. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/2396.

MLA Handbook (7th Edition):

Robertson, John Gray. “Endogenous metabolism of Nocardia corallina.” 1968. Web. 15 Dec 2019.

Vancouver:

Robertson JG. Endogenous metabolism of Nocardia corallina. [Internet] [Doctoral dissertation]. Massey University; 1968. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/2396.

Council of Science Editors:

Robertson JG. Endogenous metabolism of Nocardia corallina. [Doctoral Dissertation]. Massey University; 1968. Available from: http://hdl.handle.net/10179/2396


Massey University

25. Roughan, Philip Grattan. The lipid metabolism of plants.

Degree: PhD, Biochemistry, 1968, Massey University

 A method , based on the isolation of pure compounds by a combination of DEAE-cellulose and thin-layer chromatography , has been developed for the rapid… (more)

Subjects/Keywords: Plant metabolism; Lipids; Mesotaenium caldariorum

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APA (6th Edition):

Roughan, P. G. (1968). The lipid metabolism of plants. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/2400

Chicago Manual of Style (16th Edition):

Roughan, Philip Grattan. “The lipid metabolism of plants.” 1968. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/2400.

MLA Handbook (7th Edition):

Roughan, Philip Grattan. “The lipid metabolism of plants.” 1968. Web. 15 Dec 2019.

Vancouver:

Roughan PG. The lipid metabolism of plants. [Internet] [Doctoral dissertation]. Massey University; 1968. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/2400.

Council of Science Editors:

Roughan PG. The lipid metabolism of plants. [Doctoral Dissertation]. Massey University; 1968. Available from: http://hdl.handle.net/10179/2400


Massey University

26. Crow, Kathryn Elizabeth. Acetaldehyde metabolism in mammals.

Degree: PhD, Biochemistry, 1975, Massey University

 The metabolism of acetaldehyde in mammalian systems has been investigated both with in vitro studies on sheep liver aldehyde dehydrogenase, and by following changes in… (more)

Subjects/Keywords: Acetaldehyde; Metabolism; Mammals; Biochemistry

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APA (6th Edition):

Crow, K. E. (1975). Acetaldehyde metabolism in mammals. (Doctoral Dissertation). Massey University. Retrieved from http://hdl.handle.net/10179/3790

Chicago Manual of Style (16th Edition):

Crow, Kathryn Elizabeth. “Acetaldehyde metabolism in mammals.” 1975. Doctoral Dissertation, Massey University. Accessed December 15, 2019. http://hdl.handle.net/10179/3790.

MLA Handbook (7th Edition):

Crow, Kathryn Elizabeth. “Acetaldehyde metabolism in mammals.” 1975. Web. 15 Dec 2019.

Vancouver:

Crow KE. Acetaldehyde metabolism in mammals. [Internet] [Doctoral dissertation]. Massey University; 1975. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10179/3790.

Council of Science Editors:

Crow KE. Acetaldehyde metabolism in mammals. [Doctoral Dissertation]. Massey University; 1975. Available from: http://hdl.handle.net/10179/3790


Virginia Tech

27. Denloye, Titilola Ifeoma. Characterization of a glycerophosphodiester phosphodiesterase in the human malaria parasite Plasmodium falciparum.

Degree: PhD, Biochemistry, 2012, Virginia Tech

 Active lipid metabolism is a key process required for the intra-erythrocytic development of the malaria parasite, Plasmodium falciparum. Enzymes that hydrolyze host-derived lipids play key… (more)

Subjects/Keywords: choline; lipid metabolism; fatty acid; malaria; glycerophosphodiester phosphodiesterase; Plasmodium falciparum

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APA (6th Edition):

Denloye, T. I. (2012). Characterization of a glycerophosphodiester phosphodiesterase in the human malaria parasite Plasmodium falciparum. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77090

Chicago Manual of Style (16th Edition):

Denloye, Titilola Ifeoma. “Characterization of a glycerophosphodiester phosphodiesterase in the human malaria parasite Plasmodium falciparum.” 2012. Doctoral Dissertation, Virginia Tech. Accessed December 15, 2019. http://hdl.handle.net/10919/77090.

MLA Handbook (7th Edition):

Denloye, Titilola Ifeoma. “Characterization of a glycerophosphodiester phosphodiesterase in the human malaria parasite Plasmodium falciparum.” 2012. Web. 15 Dec 2019.

Vancouver:

Denloye TI. Characterization of a glycerophosphodiester phosphodiesterase in the human malaria parasite Plasmodium falciparum. [Internet] [Doctoral dissertation]. Virginia Tech; 2012. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10919/77090.

Council of Science Editors:

Denloye TI. Characterization of a glycerophosphodiester phosphodiesterase in the human malaria parasite Plasmodium falciparum. [Doctoral Dissertation]. Virginia Tech; 2012. Available from: http://hdl.handle.net/10919/77090


Boston University

28. Pastore, Edward Joseph. Metabolism of acetate by human leukocytes.

Degree: PhD, Biochemistry, 1959, Boston University

 The purpose of this investigation was to study the metabolism of normal human leukocytes. Leukocytes were incubated in vitro with c14-labeled acetate, and the fate… (more)

Subjects/Keywords: Human leukocyte antigen; Metabolism

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APA (6th Edition):

Pastore, E. J. (1959). Metabolism of acetate by human leukocytes. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/22492

Chicago Manual of Style (16th Edition):

Pastore, Edward Joseph. “Metabolism of acetate by human leukocytes.” 1959. Doctoral Dissertation, Boston University. Accessed December 15, 2019. http://hdl.handle.net/2144/22492.

MLA Handbook (7th Edition):

Pastore, Edward Joseph. “Metabolism of acetate by human leukocytes.” 1959. Web. 15 Dec 2019.

Vancouver:

Pastore EJ. Metabolism of acetate by human leukocytes. [Internet] [Doctoral dissertation]. Boston University; 1959. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2144/22492.

Council of Science Editors:

Pastore EJ. Metabolism of acetate by human leukocytes. [Doctoral Dissertation]. Boston University; 1959. Available from: http://hdl.handle.net/2144/22492


Boston University

29. Li, Chendi. Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes.

Degree: PhD, Biochemistry, 2015, Boston University

 Thermogenic brown adipose tissue generates heat via mitochondrial uncoupling protein-1 (UCP-1), increases whole-body energy expenditure and may protects against obesity and metabolic disorders. White adipocytes… (more)

Subjects/Keywords: Biochemistry; Beige adipocyte; MRTFA; UCP-1; Whole-body metabolism

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APA (6th Edition):

Li, C. (2015). Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16110

Chicago Manual of Style (16th Edition):

Li, Chendi. “Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes.” 2015. Doctoral Dissertation, Boston University. Accessed December 15, 2019. http://hdl.handle.net/2144/16110.

MLA Handbook (7th Edition):

Li, Chendi. “Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes.” 2015. Web. 15 Dec 2019.

Vancouver:

Li C. Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2144/16110.

Council of Science Editors:

Li C. Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16110


University of Iowa

30. Chi, Xun. Extracellular regulation of LPL activity by angiopoietin-like proteins.

Degree: PhD, Biochemistry, 2017, University of Iowa

  Dyslipidemia often accompanies metabolic diseases such as obesity and type II diabetes mellitus and represents a risk factor for cardiovascular disease. Clearance of triglycerides… (more)

Subjects/Keywords: angiopoietin-like protein; chylomicrons; lipid metabolism; LPL; plasma triglycerides; Biochemistry

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APA (6th Edition):

Chi, X. (2017). Extracellular regulation of LPL activity by angiopoietin-like proteins. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5729

Chicago Manual of Style (16th Edition):

Chi, Xun. “Extracellular regulation of LPL activity by angiopoietin-like proteins.” 2017. Doctoral Dissertation, University of Iowa. Accessed December 15, 2019. https://ir.uiowa.edu/etd/5729.

MLA Handbook (7th Edition):

Chi, Xun. “Extracellular regulation of LPL activity by angiopoietin-like proteins.” 2017. Web. 15 Dec 2019.

Vancouver:

Chi X. Extracellular regulation of LPL activity by angiopoietin-like proteins. [Internet] [Doctoral dissertation]. University of Iowa; 2017. [cited 2019 Dec 15]. Available from: https://ir.uiowa.edu/etd/5729.

Council of Science Editors:

Chi X. Extracellular regulation of LPL activity by angiopoietin-like proteins. [Doctoral Dissertation]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/5729

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