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You searched for subject:(Enzyme kinetics). Showing records 1 – 30 of 302 total matches.

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University of Sydney

1. Collett, Michael. An allosteric network within dynamin .

Degree: 2016, University of Sydney

 Dynamins are large enzymes that catalyse the hydrolysis of GTP (GTPase activity). They assemble through oligomerisation into helical polymers during endocytosis to facilitate membrane scission… (more)

Subjects/Keywords: Dynamin; Allostery; Endocytosis; Enzyme; Kinetics

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APA (6th Edition):

Collett, M. (2016). An allosteric network within dynamin . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/15871

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):

Collett, Michael. “An allosteric network within dynamin .” 2016. Thesis, University of Sydney. Accessed September 20, 2020. http://hdl.handle.net/2123/15871.

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

MLA Handbook (7th Edition):

Collett, Michael. “An allosteric network within dynamin .” 2016. Web. 20 Sep 2020.

Vancouver:

Collett M. An allosteric network within dynamin . [Internet] [Thesis]. University of Sydney; 2016. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2123/15871.

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

Council of Science Editors:

Collett M. An allosteric network within dynamin . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/15871

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


Vanderbilt University

2. Goodman, Michael Christopher. Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis.

Degree: PhD, Chemistry, 2018, Vanderbilt University

 Polyunsaturated fatty acids can be liberated from phospholipids in the membrane bilayer and enzymatically converted to oxygenated bioactive lipid compounds that contribute to the pathology,… (more)

Subjects/Keywords: prostaglandins; cyclooxygenase; Inflammation; enzyme kinetics

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APA (6th Edition):

Goodman, M. C. (2018). Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10966

Chicago Manual of Style (16th Edition):

Goodman, Michael Christopher. “Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/10966.

MLA Handbook (7th Edition):

Goodman, Michael Christopher. “Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis.” 2018. Web. 20 Sep 2020.

Vancouver:

Goodman MC. Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/10966.

Council of Science Editors:

Goodman MC. Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/10966


Iowa State University

3. Dotas, Rochelle Rea. Characterization of the C-terminal binding domain from bacterial Enzyme I.

Degree: 2020, Iowa State University

 Modulation of enzyme structure and flexibility by substrate/ligand binding provides an important source of enzyme function regulation. Unfortunately, our understanding of the fundamental mechanisms coupling… (more)

Subjects/Keywords: Dynamics; Enzyme; Kinetics; NMR; Protein

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APA (6th Edition):

Dotas, R. R. (2020). Characterization of the C-terminal binding domain from bacterial Enzyme I. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/17981

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):

Dotas, Rochelle Rea. “Characterization of the C-terminal binding domain from bacterial Enzyme I.” 2020. Thesis, Iowa State University. Accessed September 20, 2020. https://lib.dr.iastate.edu/etd/17981.

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

MLA Handbook (7th Edition):

Dotas, Rochelle Rea. “Characterization of the C-terminal binding domain from bacterial Enzyme I.” 2020. Web. 20 Sep 2020.

Vancouver:

Dotas RR. Characterization of the C-terminal binding domain from bacterial Enzyme I. [Internet] [Thesis]. Iowa State University; 2020. [cited 2020 Sep 20]. Available from: https://lib.dr.iastate.edu/etd/17981.

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

Council of Science Editors:

Dotas RR. Characterization of the C-terminal binding domain from bacterial Enzyme I. [Thesis]. Iowa State University; 2020. Available from: https://lib.dr.iastate.edu/etd/17981

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


Wilfrid Laurier University

4. Ngo, Maria. THE KINETIC CHARACTERIZATION OF TWO PUTATIVE GALACTOSIDASES, BT2857 AND SCO6594, AND THE PRELIMINARY ANALYSES OF SCO6595-97.

Degree: 2016, Wilfrid Laurier University

 Bacteroides thetaiotaomicron is a prolific bacterium found in the distal intestinal tract of humans that possesses the ability to breakdown complex polysaccharides through the release… (more)

Subjects/Keywords: carbohydrates; enzyme kinetics; galactosidases; Biochemistry

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APA (6th Edition):

Ngo, M. (2016). THE KINETIC CHARACTERIZATION OF TWO PUTATIVE GALACTOSIDASES, BT2857 AND SCO6594, AND THE PRELIMINARY ANALYSES OF SCO6595-97. (Thesis). Wilfrid Laurier University. Retrieved from https://scholars.wlu.ca/etd/1855

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):

Ngo, Maria. “THE KINETIC CHARACTERIZATION OF TWO PUTATIVE GALACTOSIDASES, BT2857 AND SCO6594, AND THE PRELIMINARY ANALYSES OF SCO6595-97.” 2016. Thesis, Wilfrid Laurier University. Accessed September 20, 2020. https://scholars.wlu.ca/etd/1855.

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

MLA Handbook (7th Edition):

Ngo, Maria. “THE KINETIC CHARACTERIZATION OF TWO PUTATIVE GALACTOSIDASES, BT2857 AND SCO6594, AND THE PRELIMINARY ANALYSES OF SCO6595-97.” 2016. Web. 20 Sep 2020.

Vancouver:

Ngo M. THE KINETIC CHARACTERIZATION OF TWO PUTATIVE GALACTOSIDASES, BT2857 AND SCO6594, AND THE PRELIMINARY ANALYSES OF SCO6595-97. [Internet] [Thesis]. Wilfrid Laurier University; 2016. [cited 2020 Sep 20]. Available from: https://scholars.wlu.ca/etd/1855.

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

Council of Science Editors:

Ngo M. THE KINETIC CHARACTERIZATION OF TWO PUTATIVE GALACTOSIDASES, BT2857 AND SCO6594, AND THE PRELIMINARY ANALYSES OF SCO6595-97. [Thesis]. Wilfrid Laurier University; 2016. Available from: https://scholars.wlu.ca/etd/1855

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


Louisiana State University

5. Calixte, Nyote J. From Micro- to Nano-Scale: Applications of Solid-Phase Enzymatic Reactors for Biopolymer Disassembly.

Degree: PhD, Chemistry, 2014, Louisiana State University

  The process of immobilizing enzymes onto solid supports for bioreactions has some compelling advantages compared to their solution-based counterpart including the facile separation of… (more)

Subjects/Keywords: kinetics; microscale; nanoscale; immobilization; enzyme

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APA (6th Edition):

Calixte, N. J. (2014). From Micro- to Nano-Scale: Applications of Solid-Phase Enzymatic Reactors for Biopolymer Disassembly. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-08272014-211241 ; https://digitalcommons.lsu.edu/gradschool_dissertations/924

Chicago Manual of Style (16th Edition):

Calixte, Nyote J. “From Micro- to Nano-Scale: Applications of Solid-Phase Enzymatic Reactors for Biopolymer Disassembly.” 2014. Doctoral Dissertation, Louisiana State University. Accessed September 20, 2020. etd-08272014-211241 ; https://digitalcommons.lsu.edu/gradschool_dissertations/924.

MLA Handbook (7th Edition):

Calixte, Nyote J. “From Micro- to Nano-Scale: Applications of Solid-Phase Enzymatic Reactors for Biopolymer Disassembly.” 2014. Web. 20 Sep 2020.

Vancouver:

Calixte NJ. From Micro- to Nano-Scale: Applications of Solid-Phase Enzymatic Reactors for Biopolymer Disassembly. [Internet] [Doctoral dissertation]. Louisiana State University; 2014. [cited 2020 Sep 20]. Available from: etd-08272014-211241 ; https://digitalcommons.lsu.edu/gradschool_dissertations/924.

Council of Science Editors:

Calixte NJ. From Micro- to Nano-Scale: Applications of Solid-Phase Enzymatic Reactors for Biopolymer Disassembly. [Doctoral Dissertation]. Louisiana State University; 2014. Available from: etd-08272014-211241 ; https://digitalcommons.lsu.edu/gradschool_dissertations/924

6. NC DOCKS at The University of North Carolina at Greensboro; Tai, Henry. Calcium and chloride function in oxygen evolution by photosystem II through bisubstrate enzyme kinetics and EPR spectroscopy of fluoride inhibition.

Degree: 2013, NC Docks

 Photosystem II (PSII) is the light-harvesting water oxidase of thylakoid membranes. The catalytic center where oxygen forms in PSII is located at the manganese cluster,… (more)

Subjects/Keywords: Enzyme kinetics; Photosynthetic oxygen evolution

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APA (6th Edition):

NC DOCKS at The University of North Carolina at Greensboro; Tai, H. (2013). Calcium and chloride function in oxygen evolution by photosystem II through bisubstrate enzyme kinetics and EPR spectroscopy of fluoride inhibition. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/uncg/f/Tai_uncg_0154M_11359.pdf

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

Chicago Manual of Style (16th Edition):

NC DOCKS at The University of North Carolina at Greensboro; Tai, Henry. “Calcium and chloride function in oxygen evolution by photosystem II through bisubstrate enzyme kinetics and EPR spectroscopy of fluoride inhibition.” 2013. Thesis, NC Docks. Accessed September 20, 2020. http://libres.uncg.edu/ir/uncg/f/Tai_uncg_0154M_11359.pdf.

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

MLA Handbook (7th Edition):

NC DOCKS at The University of North Carolina at Greensboro; Tai, Henry. “Calcium and chloride function in oxygen evolution by photosystem II through bisubstrate enzyme kinetics and EPR spectroscopy of fluoride inhibition.” 2013. Web. 20 Sep 2020.

Vancouver:

NC DOCKS at The University of North Carolina at Greensboro; Tai H. Calcium and chloride function in oxygen evolution by photosystem II through bisubstrate enzyme kinetics and EPR spectroscopy of fluoride inhibition. [Internet] [Thesis]. NC Docks; 2013. [cited 2020 Sep 20]. Available from: http://libres.uncg.edu/ir/uncg/f/Tai_uncg_0154M_11359.pdf.

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

Council of Science Editors:

NC DOCKS at The University of North Carolina at Greensboro; Tai H. Calcium and chloride function in oxygen evolution by photosystem II through bisubstrate enzyme kinetics and EPR spectroscopy of fluoride inhibition. [Thesis]. NC Docks; 2013. Available from: http://libres.uncg.edu/ir/uncg/f/Tai_uncg_0154M_11359.pdf

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


University of Utah

7. Jin, Qian. Unzipping kinetics of duplex DNA containing lesions in a nanopore and its application in monitoring an enzyme reaction.

Degree: PhD, Chemistry, 2013, University of Utah

 The dissertation presents biophysical studies of duplex DNA during unzipping in a protein ion channel and its application in the fast readout of enzyme activity.Chapter… (more)

Subjects/Keywords: DNA lesions; Enzyme kinetics; Nanopore; Unzipping kinetics

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APA (6th Edition):

Jin, Q. (2013). Unzipping kinetics of duplex DNA containing lesions in a nanopore and its application in monitoring an enzyme reaction. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2546/rec/2838

Chicago Manual of Style (16th Edition):

Jin, Qian. “Unzipping kinetics of duplex DNA containing lesions in a nanopore and its application in monitoring an enzyme reaction.” 2013. Doctoral Dissertation, University of Utah. Accessed September 20, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2546/rec/2838.

MLA Handbook (7th Edition):

Jin, Qian. “Unzipping kinetics of duplex DNA containing lesions in a nanopore and its application in monitoring an enzyme reaction.” 2013. Web. 20 Sep 2020.

Vancouver:

Jin Q. Unzipping kinetics of duplex DNA containing lesions in a nanopore and its application in monitoring an enzyme reaction. [Internet] [Doctoral dissertation]. University of Utah; 2013. [cited 2020 Sep 20]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2546/rec/2838.

Council of Science Editors:

Jin Q. Unzipping kinetics of duplex DNA containing lesions in a nanopore and its application in monitoring an enzyme reaction. [Doctoral Dissertation]. University of Utah; 2013. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2546/rec/2838


University of Otago

8. Siakkou, Eleni. Kinetics of Cysteine Dioxygenase .

Degree: 2011, University of Otago

 Cysteine dioxygenase (CDO) is a non-heme mono-iron enzyme, which catalyses the first step of cysteine metabolism in various species. It is known that malfunction of… (more)

Subjects/Keywords: cysteine dioxygenase; enzyme activity assay; enzyme kinetics; non-heme iron enzyme

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APA (6th Edition):

Siakkou, E. (2011). Kinetics of Cysteine Dioxygenase . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/1932

Chicago Manual of Style (16th Edition):

Siakkou, Eleni. “Kinetics of Cysteine Dioxygenase .” 2011. Doctoral Dissertation, University of Otago. Accessed September 20, 2020. http://hdl.handle.net/10523/1932.

MLA Handbook (7th Edition):

Siakkou, Eleni. “Kinetics of Cysteine Dioxygenase .” 2011. Web. 20 Sep 2020.

Vancouver:

Siakkou E. Kinetics of Cysteine Dioxygenase . [Internet] [Doctoral dissertation]. University of Otago; 2011. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10523/1932.

Council of Science Editors:

Siakkou E. Kinetics of Cysteine Dioxygenase . [Doctoral Dissertation]. University of Otago; 2011. Available from: http://hdl.handle.net/10523/1932


Stellenbosch University

9. Seleme, Raphahle Nthabiseng. Modelling of enzymatic protein hydrolysis.

Degree: MEng, Process Engineering, 2019, Stellenbosch University

 ENGLISH ABSTRACT: Enzymatic hydrolysis is a method which is used to produce nutritional supplements, aquaculture feed, plant fertilisers and food ingredients. Mathematical modelling of enzymatic… (more)

Subjects/Keywords: Enzymatic analysis; Hydrolysis; Isothermal calorimetry; Enzyme kinetics

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APA (6th Edition):

Seleme, R. N. (2019). Modelling of enzymatic protein hydrolysis. (Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/106159

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):

Seleme, Raphahle Nthabiseng. “Modelling of enzymatic protein hydrolysis.” 2019. Thesis, Stellenbosch University. Accessed September 20, 2020. http://hdl.handle.net/10019.1/106159.

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

MLA Handbook (7th Edition):

Seleme, Raphahle Nthabiseng. “Modelling of enzymatic protein hydrolysis.” 2019. Web. 20 Sep 2020.

Vancouver:

Seleme RN. Modelling of enzymatic protein hydrolysis. [Internet] [Thesis]. Stellenbosch University; 2019. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10019.1/106159.

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

Council of Science Editors:

Seleme RN. Modelling of enzymatic protein hydrolysis. [Thesis]. Stellenbosch University; 2019. Available from: http://hdl.handle.net/10019.1/106159

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


The Ohio State University

10. Spears, Jessica Lynn. <i>Trypanosoma brucei</i> tRNA Editing Deaminase: Conserved Deaminase Core, Unique Deaminase Features.

Degree: PhD, Microbiology, 2011, The Ohio State University

  Inosine, a guanosine analog, has been known to function in transfer RNAs (tRNAs) for decades. When inosine occurs at the wobble position of the… (more)

Subjects/Keywords: Biochemistry; Microbiology; tRNA; deaminase; ADAT; enzyme kinetics

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APA (6th Edition):

Spears, J. L. (2011). <i>Trypanosoma brucei</i> tRNA Editing Deaminase: Conserved Deaminase Core, Unique Deaminase Features. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1306848166

Chicago Manual of Style (16th Edition):

Spears, Jessica Lynn. “<i>Trypanosoma brucei</i> tRNA Editing Deaminase: Conserved Deaminase Core, Unique Deaminase Features.” 2011. Doctoral Dissertation, The Ohio State University. Accessed September 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1306848166.

MLA Handbook (7th Edition):

Spears, Jessica Lynn. “<i>Trypanosoma brucei</i> tRNA Editing Deaminase: Conserved Deaminase Core, Unique Deaminase Features.” 2011. Web. 20 Sep 2020.

Vancouver:

Spears JL. <i>Trypanosoma brucei</i> tRNA Editing Deaminase: Conserved Deaminase Core, Unique Deaminase Features. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Sep 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306848166.

Council of Science Editors:

Spears JL. <i>Trypanosoma brucei</i> tRNA Editing Deaminase: Conserved Deaminase Core, Unique Deaminase Features. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306848166


University of Oregon

11. Graybill, Chiharu. Activity of Atypical Protein Kinase C: From Regulation to Substrate Localization.

Degree: PhD, Department of Chemistry and Biochemistry, 2014, University of Oregon

 The phosphorylation activity of protein kinases is involved in virtually all biological processes of living organisms. As uncontrolled kinase cascades cause devastating defects such as… (more)

Subjects/Keywords: aPKC; Cell Polarity; Enzyme Kinetics; Phosphorylation

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APA (6th Edition):

Graybill, C. (2014). Activity of Atypical Protein Kinase C: From Regulation to Substrate Localization. (Doctoral Dissertation). University of Oregon. Retrieved from http://hdl.handle.net/1794/17875

Chicago Manual of Style (16th Edition):

Graybill, Chiharu. “Activity of Atypical Protein Kinase C: From Regulation to Substrate Localization.” 2014. Doctoral Dissertation, University of Oregon. Accessed September 20, 2020. http://hdl.handle.net/1794/17875.

MLA Handbook (7th Edition):

Graybill, Chiharu. “Activity of Atypical Protein Kinase C: From Regulation to Substrate Localization.” 2014. Web. 20 Sep 2020.

Vancouver:

Graybill C. Activity of Atypical Protein Kinase C: From Regulation to Substrate Localization. [Internet] [Doctoral dissertation]. University of Oregon; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1794/17875.

Council of Science Editors:

Graybill C. Activity of Atypical Protein Kinase C: From Regulation to Substrate Localization. [Doctoral Dissertation]. University of Oregon; 2014. Available from: http://hdl.handle.net/1794/17875


University of Illinois – Urbana-Champaign

12. Pierre, Zakiah N. Acoustically-levitated drop reactor (ldr) employable for kinetics measurements of biochemical networks.

Degree: PhD, 0335, 2011, University of Illinois – Urbana-Champaign

 Accurate measurement of enzyme kinetics is an essential part of understanding the mechanisms of biochemical reactions. The typical means of studying such systems use stirred… (more)

Subjects/Keywords: acoustic; levitator; biochemical reactions; kinetics; enzyme; myeloperoxidase

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APA (6th Edition):

Pierre, Z. N. (2011). Acoustically-levitated drop reactor (ldr) employable for kinetics measurements of biochemical networks. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24321

Chicago Manual of Style (16th Edition):

Pierre, Zakiah N. “Acoustically-levitated drop reactor (ldr) employable for kinetics measurements of biochemical networks.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 20, 2020. http://hdl.handle.net/2142/24321.

MLA Handbook (7th Edition):

Pierre, Zakiah N. “Acoustically-levitated drop reactor (ldr) employable for kinetics measurements of biochemical networks.” 2011. Web. 20 Sep 2020.

Vancouver:

Pierre ZN. Acoustically-levitated drop reactor (ldr) employable for kinetics measurements of biochemical networks. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2142/24321.

Council of Science Editors:

Pierre ZN. Acoustically-levitated drop reactor (ldr) employable for kinetics measurements of biochemical networks. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24321


University of Bath

13. Barnes, John Ashley. Theoretical modelling of transition states for chemical processes : application to enzymic and non-enzymic glycosidic hydrolysis.

Degree: PhD, 1994, University of Bath

Subjects/Keywords: 572; Enzyme kinetics

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APA (6th Edition):

Barnes, J. A. (1994). Theoretical modelling of transition states for chemical processes : application to enzymic and non-enzymic glycosidic hydrolysis. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/theoretical-modelling-of-transition-states-for-chemical-processes-application-to-enzymic-and-nonenzymic-glycosidic-hydrolysis(7db8bf80-0e6a-4598-8066-bb5a53d88b92).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261066

Chicago Manual of Style (16th Edition):

Barnes, John Ashley. “Theoretical modelling of transition states for chemical processes : application to enzymic and non-enzymic glycosidic hydrolysis.” 1994. Doctoral Dissertation, University of Bath. Accessed September 20, 2020. https://researchportal.bath.ac.uk/en/studentthesis/theoretical-modelling-of-transition-states-for-chemical-processes-application-to-enzymic-and-nonenzymic-glycosidic-hydrolysis(7db8bf80-0e6a-4598-8066-bb5a53d88b92).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261066.

MLA Handbook (7th Edition):

Barnes, John Ashley. “Theoretical modelling of transition states for chemical processes : application to enzymic and non-enzymic glycosidic hydrolysis.” 1994. Web. 20 Sep 2020.

Vancouver:

Barnes JA. Theoretical modelling of transition states for chemical processes : application to enzymic and non-enzymic glycosidic hydrolysis. [Internet] [Doctoral dissertation]. University of Bath; 1994. [cited 2020 Sep 20]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/theoretical-modelling-of-transition-states-for-chemical-processes-application-to-enzymic-and-nonenzymic-glycosidic-hydrolysis(7db8bf80-0e6a-4598-8066-bb5a53d88b92).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261066.

Council of Science Editors:

Barnes JA. Theoretical modelling of transition states for chemical processes : application to enzymic and non-enzymic glycosidic hydrolysis. [Doctoral Dissertation]. University of Bath; 1994. Available from: https://researchportal.bath.ac.uk/en/studentthesis/theoretical-modelling-of-transition-states-for-chemical-processes-application-to-enzymic-and-nonenzymic-glycosidic-hydrolysis(7db8bf80-0e6a-4598-8066-bb5a53d88b92).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261066


Lehigh University

14. McDermott, Jack Wade. Inversion of Sucrose by Invertase and the Separation of Fructose and Glucose by Ion Exchange Chromatography.

Degree: MS, Chemical Engineering, 2020, Lehigh University

  The primary goal of this thesis is to present a fundamental understanding of ion exchange chromatography and enzyme kinetics. Both techniques are explored through… (more)

Subjects/Keywords: Enzyme Kinetics; Ion Exchange Chromatography; Chemical Engineering

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APA (6th Edition):

McDermott, J. W. (2020). Inversion of Sucrose by Invertase and the Separation of Fructose and Glucose by Ion Exchange Chromatography. (Thesis). Lehigh University. Retrieved from https://preserve.lehigh.edu/etd/5685

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):

McDermott, Jack Wade. “Inversion of Sucrose by Invertase and the Separation of Fructose and Glucose by Ion Exchange Chromatography.” 2020. Thesis, Lehigh University. Accessed September 20, 2020. https://preserve.lehigh.edu/etd/5685.

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

MLA Handbook (7th Edition):

McDermott, Jack Wade. “Inversion of Sucrose by Invertase and the Separation of Fructose and Glucose by Ion Exchange Chromatography.” 2020. Web. 20 Sep 2020.

Vancouver:

McDermott JW. Inversion of Sucrose by Invertase and the Separation of Fructose and Glucose by Ion Exchange Chromatography. [Internet] [Thesis]. Lehigh University; 2020. [cited 2020 Sep 20]. Available from: https://preserve.lehigh.edu/etd/5685.

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

Council of Science Editors:

McDermott JW. Inversion of Sucrose by Invertase and the Separation of Fructose and Glucose by Ion Exchange Chromatography. [Thesis]. Lehigh University; 2020. Available from: https://preserve.lehigh.edu/etd/5685

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


Louisiana State University

15. Evans, Alexandra Leigh. The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase.

Degree: PhD, Biochemistry, 2018, Louisiana State University

  Metabolic Regulation is a complex system used to control cellular metabolism in response to conditions in the cell’s environment. For most enzymes, the cell… (more)

Subjects/Keywords: Acetyl-CoA Carboxylase; Enzyme; Kinetics; Protein; Regulation

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APA (6th Edition):

Evans, A. L. (2018). The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase. (Doctoral Dissertation). Louisiana State University. Retrieved from https://digitalcommons.lsu.edu/gradschool_dissertations/4701

Chicago Manual of Style (16th Edition):

Evans, Alexandra Leigh. “The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase.” 2018. Doctoral Dissertation, Louisiana State University. Accessed September 20, 2020. https://digitalcommons.lsu.edu/gradschool_dissertations/4701.

MLA Handbook (7th Edition):

Evans, Alexandra Leigh. “The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase.” 2018. Web. 20 Sep 2020.

Vancouver:

Evans AL. The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase. [Internet] [Doctoral dissertation]. Louisiana State University; 2018. [cited 2020 Sep 20]. Available from: https://digitalcommons.lsu.edu/gradschool_dissertations/4701.

Council of Science Editors:

Evans AL. The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase. [Doctoral Dissertation]. Louisiana State University; 2018. Available from: https://digitalcommons.lsu.edu/gradschool_dissertations/4701


University of Georgia

16. Bottjen, Rachel Christine. Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens.

Degree: 2014, University of Georgia

 The Microplitis demolitor bracovirus (MdBV) genome contains a large protein tyrosine phosphatase (PTP) gene family that encodes four enzymes with intact catalytic domains, including ptp-H2.… (more)

Subjects/Keywords: polydnavirus; phosphatase; enzyme kinetics; metabolism dysregulation

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APA (6th Edition):

Bottjen, R. C. (2014). Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/27067

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):

Bottjen, Rachel Christine. “Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens.” 2014. Thesis, University of Georgia. Accessed September 20, 2020. http://hdl.handle.net/10724/27067.

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

MLA Handbook (7th Edition):

Bottjen, Rachel Christine. “Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens.” 2014. Web. 20 Sep 2020.

Vancouver:

Bottjen RC. Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/10724/27067.

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

Council of Science Editors:

Bottjen RC. Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/27067

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


University of Illinois – Urbana-Champaign

17. Hung, John. Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase.

Degree: PhD, 0335, 2014, University of Illinois – Urbana-Champaign

 Phosphite dehydrogenase (PTDH) catalyzes the oxidation of phosphite to phosphate with the concurrent reduction of NAD+ to NADH. The mechanism of the reaction resembles a… (more)

Subjects/Keywords: Phosphite Dehydrogenase; enzymology; chemical biology; enzymes; enzyme kinetics; enzyme inhibition

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APA (6th Edition):

Hung, J. (2014). Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46929

Chicago Manual of Style (16th Edition):

Hung, John. “Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 20, 2020. http://hdl.handle.net/2142/46929.

MLA Handbook (7th Edition):

Hung, John. “Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase.” 2014. Web. 20 Sep 2020.

Vancouver:

Hung J. Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2142/46929.

Council of Science Editors:

Hung J. Mechanistic studies to determine the catalytic roles of active site residues in phosphite dehydrogenase. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46929


Louisiana State University

18. Henken, Rachel. Studies of Enzyme Kinetics and Inhibition Through Capillary Electrophoretic Enzyme Assays.

Degree: PhD, Chemistry, 2013, Louisiana State University

Enzyme assays are used throughout the biological, chemical, and medical sciences for the study of enzymes, and typically are performed by bulk solution measurements in… (more)

Subjects/Keywords: enzyme; kinetics; inhibition; CE; enzyme assay; capillary electrophoresis; EMMA

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APA (6th Edition):

Henken, R. (2013). Studies of Enzyme Kinetics and Inhibition Through Capillary Electrophoretic Enzyme Assays. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-01172014-150850 ; https://digitalcommons.lsu.edu/gradschool_dissertations/5

Chicago Manual of Style (16th Edition):

Henken, Rachel. “Studies of Enzyme Kinetics and Inhibition Through Capillary Electrophoretic Enzyme Assays.” 2013. Doctoral Dissertation, Louisiana State University. Accessed September 20, 2020. etd-01172014-150850 ; https://digitalcommons.lsu.edu/gradschool_dissertations/5.

MLA Handbook (7th Edition):

Henken, Rachel. “Studies of Enzyme Kinetics and Inhibition Through Capillary Electrophoretic Enzyme Assays.” 2013. Web. 20 Sep 2020.

Vancouver:

Henken R. Studies of Enzyme Kinetics and Inhibition Through Capillary Electrophoretic Enzyme Assays. [Internet] [Doctoral dissertation]. Louisiana State University; 2013. [cited 2020 Sep 20]. Available from: etd-01172014-150850 ; https://digitalcommons.lsu.edu/gradschool_dissertations/5.

Council of Science Editors:

Henken R. Studies of Enzyme Kinetics and Inhibition Through Capillary Electrophoretic Enzyme Assays. [Doctoral Dissertation]. Louisiana State University; 2013. Available from: etd-01172014-150850 ; https://digitalcommons.lsu.edu/gradschool_dissertations/5


University of Michigan

19. Schroeder, McKenna. Immobilized Enzymes: Activity, Orientation, and Stability.

Degree: PhD, Chemical Biology, 2016, University of Michigan

Enzyme immobilization is an important tool for many industrial and medical fields applications as well as biosensors. Much work has been done developing types of… (more)

Subjects/Keywords: Immobilized enzymes; Nitroreductase; Self-assembling monolayers; Enzyme kinetics; Enzyme stability; Enzyme orientation; Biological Chemistry; Science

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APA (6th Edition):

Schroeder, M. (2016). Immobilized Enzymes: Activity, Orientation, and Stability. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/135760

Chicago Manual of Style (16th Edition):

Schroeder, McKenna. “Immobilized Enzymes: Activity, Orientation, and Stability.” 2016. Doctoral Dissertation, University of Michigan. Accessed September 20, 2020. http://hdl.handle.net/2027.42/135760.

MLA Handbook (7th Edition):

Schroeder, McKenna. “Immobilized Enzymes: Activity, Orientation, and Stability.” 2016. Web. 20 Sep 2020.

Vancouver:

Schroeder M. Immobilized Enzymes: Activity, Orientation, and Stability. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2027.42/135760.

Council of Science Editors:

Schroeder M. Immobilized Enzymes: Activity, Orientation, and Stability. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/135760


Vanderbilt University

20. Selvy, Paige Elizabeth. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D.

Degree: PhD, Pharmacology, 2011, Vanderbilt University

 Increasing evidence supports an integral role for the lipid second messenger phosphatidic acid (PtdOH) in cell signaling. In addition to altering curvature of biological membranes,… (more)

Subjects/Keywords: small molecule inhibitor; phospholipase D; mechanism; interfacial kinetics; enzyme kinetics; lipids

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APA (6th Edition):

Selvy, P. E. (2011). Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14456

Chicago Manual of Style (16th Edition):

Selvy, Paige Elizabeth. “Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed September 20, 2020. http://hdl.handle.net/1803/14456.

MLA Handbook (7th Edition):

Selvy, Paige Elizabeth. “Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D.” 2011. Web. 20 Sep 2020.

Vancouver:

Selvy PE. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1803/14456.

Council of Science Editors:

Selvy PE. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/14456


Texas Tech University

21. Nguyen, Tuan. Comparison of five kinetic parameter retrieval techniques which are derived from the Michaelis-Menten enzyme kinetic model.

Degree: 1989, Texas Tech University

 A study of least-squares estimation of Michaelis-Menten kinetic parameters Km and Vmax was performed using five kinetic parameter retrieval techniques. These techniques are derived from… (more)

Subjects/Keywords: Enzyme kinetics; Chemical kinetics

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APA (6th Edition):

Nguyen, T. (1989). Comparison of five kinetic parameter retrieval techniques which are derived from the Michaelis-Menten enzyme kinetic model. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/10205

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):

Nguyen, Tuan. “Comparison of five kinetic parameter retrieval techniques which are derived from the Michaelis-Menten enzyme kinetic model.” 1989. Thesis, Texas Tech University. Accessed September 20, 2020. http://hdl.handle.net/2346/10205.

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

MLA Handbook (7th Edition):

Nguyen, Tuan. “Comparison of five kinetic parameter retrieval techniques which are derived from the Michaelis-Menten enzyme kinetic model.” 1989. Web. 20 Sep 2020.

Vancouver:

Nguyen T. Comparison of five kinetic parameter retrieval techniques which are derived from the Michaelis-Menten enzyme kinetic model. [Internet] [Thesis]. Texas Tech University; 1989. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2346/10205.

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

Council of Science Editors:

Nguyen T. Comparison of five kinetic parameter retrieval techniques which are derived from the Michaelis-Menten enzyme kinetic model. [Thesis]. Texas Tech University; 1989. Available from: http://hdl.handle.net/2346/10205

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


McMaster University

22. Balachandran, Naresh. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase.

Degree: PhD, 2014, McMaster University

The rise of bacterial infections and increase of antibiotic resistant bacteria has become a major problem in the treatment of bacterial infections. The use… (more)

Subjects/Keywords: enzyme kinetics; mechanism; drug design; x-ray crystallography; enzyme dynamics; Biochemistry; Biochemistry

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

APA (6th Edition):

Balachandran, N. (2014). DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/14139

Chicago Manual of Style (16th Edition):

Balachandran, Naresh. “DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase.” 2014. Doctoral Dissertation, McMaster University. Accessed September 20, 2020. http://hdl.handle.net/11375/14139.

MLA Handbook (7th Edition):

Balachandran, Naresh. “DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase.” 2014. Web. 20 Sep 2020.

Vancouver:

Balachandran N. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/11375/14139.

Council of Science Editors:

Balachandran N. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. [Doctoral Dissertation]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/14139


Penn State University

23. Zaccardi, Margot Joan. mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase.

Degree: 2013, Penn State University

 The design and production of enzymes that are capable of performing reactions in an industrial setting is of profound importance for the advancement of technologies… (more)

Subjects/Keywords: indole-3-glycerol phosphate synthase; enzyme kinetics; mechanism of IGPS; thermophilic enzymes; enzyme engineering

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APA (6th Edition):

Zaccardi, M. J. (2013). mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/19225

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):

Zaccardi, Margot Joan. “mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase.” 2013. Thesis, Penn State University. Accessed September 20, 2020. https://submit-etda.libraries.psu.edu/catalog/19225.

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

MLA Handbook (7th Edition):

Zaccardi, Margot Joan. “mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase.” 2013. Web. 20 Sep 2020.

Vancouver:

Zaccardi MJ. mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase. [Internet] [Thesis]. Penn State University; 2013. [cited 2020 Sep 20]. Available from: https://submit-etda.libraries.psu.edu/catalog/19225.

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

Council of Science Editors:

Zaccardi MJ. mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase. [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/19225

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


Univerzitet u Beogradu

24. Žuža, Milena G., 1980-. Razvoj imobilisanih sistema sa penicilin-acilazom iz Esherichia coli za dobijanje polusintetskih penicilina.

Degree: Tehnološko-metalurški fakultet, 2013, Univerzitet u Beogradu

Hemija i hemijska tehnologija - Biohemijsko inženjerstvo i biotehnologija / Chemistry and Chemical Technology - Biochemical Engineering and Biotechnology

Osnovni cilj ove doktorske disertacije je… (more)

Subjects/Keywords: penicillin acylase; immobilization; Sepabeads carriers; enzyme modification; chitosan microbeads; enzyme biocatalysis; kinetics; bioreactors

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APA (6th Edition):

Žuža, Milena G., 1. (2013). Razvoj imobilisanih sistema sa penicilin-acilazom iz Esherichia coli za dobijanje polusintetskih penicilina. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:5526/bdef:Content/get

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):

Žuža, Milena G., 1980-. “Razvoj imobilisanih sistema sa penicilin-acilazom iz Esherichia coli za dobijanje polusintetskih penicilina.” 2013. Thesis, Univerzitet u Beogradu. Accessed September 20, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:5526/bdef:Content/get.

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

MLA Handbook (7th Edition):

Žuža, Milena G., 1980-. “Razvoj imobilisanih sistema sa penicilin-acilazom iz Esherichia coli za dobijanje polusintetskih penicilina.” 2013. Web. 20 Sep 2020.

Vancouver:

Žuža, Milena G. 1. Razvoj imobilisanih sistema sa penicilin-acilazom iz Esherichia coli za dobijanje polusintetskih penicilina. [Internet] [Thesis]. Univerzitet u Beogradu; 2013. [cited 2020 Sep 20]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:5526/bdef:Content/get.

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

Council of Science Editors:

Žuža, Milena G. 1. Razvoj imobilisanih sistema sa penicilin-acilazom iz Esherichia coli za dobijanje polusintetskih penicilina. [Thesis]. Univerzitet u Beogradu; 2013. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:5526/bdef:Content/get

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


University of New South Wales

25. Suharto, Adrian Rinaldi. Structural studies of giardial arginine deiminase.

Degree: Biotechnology and Biomolecular Sciences, 2006, University of New South Wales

 Recombinant giardial arginine deiminase (rADI) was characterized. The enzyme was found to have a specific activity of 12 U (mg protein)-1under at pH 7.4 and… (more)

Subjects/Keywords: Enzyme inhibitors; Enzyme kinetics; Giardia lamblia

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APA (6th Edition):

Suharto, A. R. (2006). Structural studies of giardial arginine deiminase. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true

Chicago Manual of Style (16th Edition):

Suharto, Adrian Rinaldi. “Structural studies of giardial arginine deiminase.” 2006. Masters Thesis, University of New South Wales. Accessed September 20, 2020. http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true.

MLA Handbook (7th Edition):

Suharto, Adrian Rinaldi. “Structural studies of giardial arginine deiminase.” 2006. Web. 20 Sep 2020.

Vancouver:

Suharto AR. Structural studies of giardial arginine deiminase. [Internet] [Masters thesis]. University of New South Wales; 2006. [cited 2020 Sep 20]. Available from: http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true.

Council of Science Editors:

Suharto AR. Structural studies of giardial arginine deiminase. [Masters Thesis]. University of New South Wales; 2006. Available from: http://handle.unsw.edu.au/1959.4/26293 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:1153/SOURCE1?view=true


Baylor University

26. Schlesinger, Sara Rae. Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes.

Degree: PhD, Chemistry and Biochemistry., 2014, Baylor University

 Pathogenic bacteria are rapidly becoming antibiotic resistant, at a rate much faster than the production and FDA approval of new antibiotics that can combat these… (more)

Subjects/Keywords: Metallo-beta-lactamase.; Antibiotic resistance.; Thiomaltol.; Protein purification.; Enzyme kinetics.; Enzyme inhibition.

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APA (6th Edition):

Schlesinger, S. R. (2014). Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes. (Doctoral Dissertation). Baylor University. Retrieved from http://hdl.handle.net/2104/9103

Chicago Manual of Style (16th Edition):

Schlesinger, Sara Rae. “Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes.” 2014. Doctoral Dissertation, Baylor University. Accessed September 20, 2020. http://hdl.handle.net/2104/9103.

MLA Handbook (7th Edition):

Schlesinger, Sara Rae. “Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes.” 2014. Web. 20 Sep 2020.

Vancouver:

Schlesinger SR. Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes. [Internet] [Doctoral dissertation]. Baylor University; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2104/9103.

Council of Science Editors:

Schlesinger SR. Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes. [Doctoral Dissertation]. Baylor University; 2014. Available from: http://hdl.handle.net/2104/9103


University of Florida

27. Yang,Soon Hye. Nanoparticle-Based Cellular Machinery for the Degradation of Specific Rna and Protein.

Degree: MS, Chemistry, 2011, University of Florida

 Nanoparticles (NPs) have been extensively studied as a novel tool for biomedicines via their unique characters such as non-toxicity, ready functionality and biomedical imaging. This… (more)

Subjects/Keywords: Coagulants; DNA; Enzyme kinetics; Enzyme substrates; Enzymes; Molecules; Nanoparticles; Oligonucleotides; Phosphates; RNA

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APA (6th Edition):

Hye, Y. (2011). Nanoparticle-Based Cellular Machinery for the Degradation of Specific Rna and Protein. (Masters Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0043404

Chicago Manual of Style (16th Edition):

Hye, Yang,Soon. “Nanoparticle-Based Cellular Machinery for the Degradation of Specific Rna and Protein.” 2011. Masters Thesis, University of Florida. Accessed September 20, 2020. https://ufdc.ufl.edu/UFE0043404.

MLA Handbook (7th Edition):

Hye, Yang,Soon. “Nanoparticle-Based Cellular Machinery for the Degradation of Specific Rna and Protein.” 2011. Web. 20 Sep 2020.

Vancouver:

Hye Y. Nanoparticle-Based Cellular Machinery for the Degradation of Specific Rna and Protein. [Internet] [Masters thesis]. University of Florida; 2011. [cited 2020 Sep 20]. Available from: https://ufdc.ufl.edu/UFE0043404.

Council of Science Editors:

Hye Y. Nanoparticle-Based Cellular Machinery for the Degradation of Specific Rna and Protein. [Masters Thesis]. University of Florida; 2011. Available from: https://ufdc.ufl.edu/UFE0043404


Case Western Reserve University

28. Frase, Hilary. TOWARDS DEVELOPING SPECIFIC INHIBITORS OF THE ATP-DEPENDENT LON PROTEASE.

Degree: PhD, Chemistry, 2007, Case Western Reserve University

 The ATP-dependent serine protease Lon is responsible for degrading damaged and certain regulatory proteins in vivo. The importance of Lon activity in bacterial pathogenicity has… (more)

Subjects/Keywords: Chemistry, Biochemistry; Lon protease; serine protease; steady-state kinetics; enzyme kinetics; time-dependent inhibition; enzyme inhibition

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APA (6th Edition):

Frase, H. (2007). TOWARDS DEVELOPING SPECIFIC INHIBITORS OF THE ATP-DEPENDENT LON PROTEASE. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1175637588

Chicago Manual of Style (16th Edition):

Frase, Hilary. “TOWARDS DEVELOPING SPECIFIC INHIBITORS OF THE ATP-DEPENDENT LON PROTEASE.” 2007. Doctoral Dissertation, Case Western Reserve University. Accessed September 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1175637588.

MLA Handbook (7th Edition):

Frase, Hilary. “TOWARDS DEVELOPING SPECIFIC INHIBITORS OF THE ATP-DEPENDENT LON PROTEASE.” 2007. Web. 20 Sep 2020.

Vancouver:

Frase H. TOWARDS DEVELOPING SPECIFIC INHIBITORS OF THE ATP-DEPENDENT LON PROTEASE. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2020 Sep 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1175637588.

Council of Science Editors:

Frase H. TOWARDS DEVELOPING SPECIFIC INHIBITORS OF THE ATP-DEPENDENT LON PROTEASE. [Doctoral Dissertation]. Case Western Reserve University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1175637588


University of North Texas

29. Lai, Chung-Jeng. Fumarate Activation and Kinetic Solvent Isotope Effects as Probes of the NAD-Malic Enzyme Reaction.

Degree: 1992, University of North Texas

 The kinetic mechanism of activation of the NAD-malic enzyme by fumarate and the transition state structure for the oxidation malate for the NAD-malic enzyme reaction… (more)

Subjects/Keywords: NAD-malic enzyme; fumarates; Chemical kinetics.; Enzyme kinetics.

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

APA (6th Edition):

Lai, C. (1992). Fumarate Activation and Kinetic Solvent Isotope Effects as Probes of the NAD-Malic Enzyme Reaction. (Thesis). University of North Texas. Retrieved from https://digital.library.unt.edu/ark:/67531/metadc278864/

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):

Lai, Chung-Jeng. “Fumarate Activation and Kinetic Solvent Isotope Effects as Probes of the NAD-Malic Enzyme Reaction.” 1992. Thesis, University of North Texas. Accessed September 20, 2020. https://digital.library.unt.edu/ark:/67531/metadc278864/.

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

MLA Handbook (7th Edition):

Lai, Chung-Jeng. “Fumarate Activation and Kinetic Solvent Isotope Effects as Probes of the NAD-Malic Enzyme Reaction.” 1992. Web. 20 Sep 2020.

Vancouver:

Lai C. Fumarate Activation and Kinetic Solvent Isotope Effects as Probes of the NAD-Malic Enzyme Reaction. [Internet] [Thesis]. University of North Texas; 1992. [cited 2020 Sep 20]. Available from: https://digital.library.unt.edu/ark:/67531/metadc278864/.

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

Council of Science Editors:

Lai C. Fumarate Activation and Kinetic Solvent Isotope Effects as Probes of the NAD-Malic Enzyme Reaction. [Thesis]. University of North Texas; 1992. Available from: https://digital.library.unt.edu/ark:/67531/metadc278864/

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


University of Wisconsin – Milwaukee

30. Hoag, Matthew Robert. Renalase as an Intracellular Metabolite Repair Enzyme.

Degree: PhD, Chemistry, 2018, University of Wisconsin – Milwaukee

  The human enzyme renalase was discovered in 2005 by nephrologist Gary Desir, who claimed the enzyme is secreted by the kidney into the blood… (more)

Subjects/Keywords: metabolite damage; metabolite repair; old yellow enzyme; pre-steady-state kinetics; renalase; transient kinetics; Biochemistry

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

APA (6th Edition):

Hoag, M. R. (2018). Renalase as an Intracellular Metabolite Repair Enzyme. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/1994

Chicago Manual of Style (16th Edition):

Hoag, Matthew Robert. “Renalase as an Intracellular Metabolite Repair Enzyme.” 2018. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed September 20, 2020. https://dc.uwm.edu/etd/1994.

MLA Handbook (7th Edition):

Hoag, Matthew Robert. “Renalase as an Intracellular Metabolite Repair Enzyme.” 2018. Web. 20 Sep 2020.

Vancouver:

Hoag MR. Renalase as an Intracellular Metabolite Repair Enzyme. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2018. [cited 2020 Sep 20]. Available from: https://dc.uwm.edu/etd/1994.

Council of Science Editors:

Hoag MR. Renalase as an Intracellular Metabolite Repair Enzyme. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2018. Available from: https://dc.uwm.edu/etd/1994

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