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You searched for subject:(Enzyme kinetics). Showing records 1 – 30 of 275 total matches.

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Louisiana State University

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

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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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


University of Sydney

2. 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 June 24, 2019. 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. 24 Jun 2019.

Vancouver:

Collett M. An allosteric network within dynamin . [Internet] [Thesis]. University of Sydney; 2016. [cited 2019 Jun 24]. 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


Wilfrid Laurier University

3. 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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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


Vanderbilt University

4. 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://etd.library.vanderbilt.edu/available/etd-03202018-132825/ ;

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 June 24, 2019. http://etd.library.vanderbilt.edu/available/etd-03202018-132825/ ;.

MLA Handbook (7th Edition):

Goodman, Michael Christopher. “Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis.” 2018. Web. 24 Jun 2019.

Vancouver:

Goodman MC. Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2019 Jun 24]. Available from: http://etd.library.vanderbilt.edu/available/etd-03202018-132825/ ;.

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://etd.library.vanderbilt.edu/available/etd-03202018-132825/ ;


University of Utah

5. 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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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

6. 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 June 24, 2019. http://hdl.handle.net/10523/1932.

MLA Handbook (7th Edition):

Siakkou, Eleni. “Kinetics of Cysteine Dioxygenase .” 2011. Web. 24 Jun 2019.

Vancouver:

Siakkou E. Kinetics of Cysteine Dioxygenase . [Internet] [Doctoral dissertation]. University of Otago; 2011. [cited 2019 Jun 24]. 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


University of Georgia

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

Degree: MS, Entomology, 2011, 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. (2011). Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/bottjen_rachel_c_201105_ms

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.” 2011. Masters Thesis, University of Georgia. Accessed June 24, 2019. http://purl.galileo.usg.edu/uga_etd/bottjen_rachel_c_201105_ms.

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.” 2011. Web. 24 Jun 2019.

Vancouver:

Bottjen RC. Characterization of the viral protein tyrosine phosphatase-H2 and the metabolic consequences of Microplitis demolitor bracoviral infection in Pseudoplusia includens. [Internet] [Masters thesis]. University of Georgia; 2011. [cited 2019 Jun 24]. Available from: http://purl.galileo.usg.edu/uga_etd/bottjen_rachel_c_201105_ms.

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. [Masters Thesis]. University of Georgia; 2011. Available from: http://purl.galileo.usg.edu/uga_etd/bottjen_rachel_c_201105_ms


Texas A&M University

8. Ralph, Erik C. The chemical mechanisms of flavin-dependent amine oxidases and the plasticity of the two-his one-carboxylate facial triad in tyrosine hydroxylase.

Degree: 2009, Texas A&M University

 Despite a number of kinetic and spectroscopic studies, the chemical mechanisms of amine oxidation by flavoenzymes remain widely debated. The mechanisms of by Nmethyltryptophan oxidase… (more)

Subjects/Keywords: flavin; enzyme; kinetics; isotope effects; oxidases

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APA (6th Edition):

Ralph, E. C. (2009). The chemical mechanisms of flavin-dependent amine oxidases and the plasticity of the two-his one-carboxylate facial triad in tyrosine hydroxylase. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1043

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):

Ralph, Erik C. “The chemical mechanisms of flavin-dependent amine oxidases and the plasticity of the two-his one-carboxylate facial triad in tyrosine hydroxylase.” 2009. Thesis, Texas A&M University. Accessed June 24, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-1043.

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

MLA Handbook (7th Edition):

Ralph, Erik C. “The chemical mechanisms of flavin-dependent amine oxidases and the plasticity of the two-his one-carboxylate facial triad in tyrosine hydroxylase.” 2009. Web. 24 Jun 2019.

Vancouver:

Ralph EC. The chemical mechanisms of flavin-dependent amine oxidases and the plasticity of the two-his one-carboxylate facial triad in tyrosine hydroxylase. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1043.

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

Council of Science Editors:

Ralph EC. The chemical mechanisms of flavin-dependent amine oxidases and the plasticity of the two-his one-carboxylate facial triad in tyrosine hydroxylase. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1043

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


The Ohio State University

9. 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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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 Bath

10. 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://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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. Available from: 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://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.261066


University of Illinois – Urbana-Champaign

11. 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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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


Louisiana State University

12. 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 June 24, 2019. 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. 24 Jun 2019.

Vancouver:

Henken R. Studies of Enzyme Kinetics and Inhibition Through Capillary Electrophoretic Enzyme Assays. [Internet] [Doctoral dissertation]. Louisiana State University; 2013. [cited 2019 Jun 24]. 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 Ottawa

13. Apperley, Kim Yang-Ping. Reversible and Photolabile Inhibitors for Human Tissue Transglutaminase .

Degree: 2017, University of Ottawa

 Tissue transglutaminase (TG2) is a calcium-dependent enzyme that natively catalyses the formation of isopeptidic bonds between protein- or peptide-bound glutamine and lysine residues. Physiologically, it… (more)

Subjects/Keywords: enzyme; transglutaminase; enzyme kinetics; photolabelling; reversible inhibition; competitive inhibition

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APA (6th Edition):

Apperley, K. Y. (2017). Reversible and Photolabile Inhibitors for Human Tissue Transglutaminase . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36593

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):

Apperley, Kim Yang-Ping. “Reversible and Photolabile Inhibitors for Human Tissue Transglutaminase .” 2017. Thesis, University of Ottawa. Accessed June 24, 2019. http://hdl.handle.net/10393/36593.

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

MLA Handbook (7th Edition):

Apperley, Kim Yang-Ping. “Reversible and Photolabile Inhibitors for Human Tissue Transglutaminase .” 2017. Web. 24 Jun 2019.

Vancouver:

Apperley KY. Reversible and Photolabile Inhibitors for Human Tissue Transglutaminase . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/10393/36593.

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

Council of Science Editors:

Apperley KY. Reversible and Photolabile Inhibitors for Human Tissue Transglutaminase . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36593

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


University of Illinois – Urbana-Champaign

14. 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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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


University of Michigan

15. 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 June 24, 2019. http://hdl.handle.net/2027.42/135760.

MLA Handbook (7th Edition):

Schroeder, McKenna. “Immobilized Enzymes: Activity, Orientation, and Stability.” 2016. Web. 24 Jun 2019.

Vancouver:

Schroeder M. Immobilized Enzymes: Activity, Orientation, and Stability. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Jun 24]. 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

16. 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://etd.library.vanderbilt.edu//available/etd-11072011-164315/ ;

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 June 24, 2019. http://etd.library.vanderbilt.edu//available/etd-11072011-164315/ ;.

MLA Handbook (7th Edition):

Selvy, Paige Elizabeth. “Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D.” 2011. Web. 24 Jun 2019.

Vancouver:

Selvy PE. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Jun 24]. Available from: http://etd.library.vanderbilt.edu//available/etd-11072011-164315/ ;.

Council of Science Editors:

Selvy PE. Mechanistic characterization of isoform selective inhibitors of mammalian phospholipase D. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu//available/etd-11072011-164315/ ;


Univerzitet u Beogradu

17. 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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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


Baylor University

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

Degree: 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. (Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/9103

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):

Schlesinger, Sara Rae. “Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes. ” 2014. Thesis, Baylor University. Accessed June 24, 2019. http://hdl.handle.net/2104/9103.

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

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. 24 Jun 2019.

Vancouver:

Schlesinger SR. Purification, characterization, and kinetic analysis of various metallo-β-lactamases and discovery of novel inhibitors of these enzymes. [Internet] [Thesis]. Baylor University; 2014. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/2104/9103.

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

Council of Science Editors:

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

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


Penn State University

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

Degree: PhD, Chemistry, 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. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/19225

Chicago Manual of Style (16th Edition):

Zaccardi, Margot Joan. “mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase.” 2013. Doctoral Dissertation, Penn State University. Accessed June 24, 2019. https://etda.libraries.psu.edu/catalog/19225.

MLA Handbook (7th Edition):

Zaccardi, Margot Joan. “mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase.” 2013. Web. 24 Jun 2019.

Vancouver:

Zaccardi MJ. mechanistic analysis of the tryptophan biosynthetic enzyme indole-3-glycerol phosphate synthase. [Internet] [Doctoral dissertation]. Penn State University; 2013. [cited 2019 Jun 24]. Available from: https://etda.libraries.psu.edu/catalog/19225.

Council of Science Editors:

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


McMaster University

20. 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 (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 June 24, 2019. http://hdl.handle.net/11375/14139.

MLA Handbook (7th Edition):

Balachandran, Naresh. “DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase.” 2014. Web. 24 Jun 2019.

Vancouver:

Balachandran N. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2019 Jun 24]. 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


University of Florida

21. 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 http://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 June 24, 2019. http://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. 24 Jun 2019.

Vancouver:

Hye Y. Nanoparticle-Based Cellular Machinery for the Degradation of Specific Rna and Protein. [Internet] [Masters thesis]. University of Florida; 2011. [cited 2019 Jun 24]. Available from: http://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: http://ufdc.ufl.edu/UFE0043404


University of New South Wales

22. 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 June 24, 2019. 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. 24 Jun 2019.

Vancouver:

Suharto AR. Structural studies of giardial arginine deiminase. [Internet] [Masters thesis]. University of New South Wales; 2006. [cited 2019 Jun 24]. 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


Case Western Reserve University

23. 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 June 24, 2019. 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. 24 Jun 2019.

Vancouver:

Frase H. TOWARDS DEVELOPING SPECIFIC INHIBITORS OF THE ATP-DEPENDENT LON PROTEASE. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2019 Jun 24]. 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

24. 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 (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 June 24, 2019. 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. 24 Jun 2019.

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 2019 Jun 24]. 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

25. 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 (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 June 24, 2019. https://dc.uwm.edu/etd/1994.

MLA Handbook (7th Edition):

Hoag, Matthew Robert. “Renalase as an Intracellular Metabolite Repair Enzyme.” 2018. Web. 24 Jun 2019.

Vancouver:

Hoag MR. Renalase as an Intracellular Metabolite Repair Enzyme. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2018. [cited 2019 Jun 24]. 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


University of Akron

26. Hancock, James. Organic Phase Entrapment of Glucose Oxidase In Polymeric Nanoparticles.

Degree: MS, Chemical Engineering, 2008, University of Akron

 Immobilizing enzymes using polymeric particles is an excellent means to increase the reusability of a biocatalyst. Recovering active enzyme free in solution is difficult. However,… (more)

Subjects/Keywords: Biochemistry; Chemical Engineering; Engineering; Particle Physics; Polymers; nanoparticle; nanotechnology; enzyme immobilization; enzyme entrapment; enzyme kinetics; polymer swelling

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APA (6th Edition):

Hancock, J. (2008). Organic Phase Entrapment of Glucose Oxidase In Polymeric Nanoparticles. (Masters Thesis). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1207860116

Chicago Manual of Style (16th Edition):

Hancock, James. “Organic Phase Entrapment of Glucose Oxidase In Polymeric Nanoparticles.” 2008. Masters Thesis, University of Akron. Accessed June 24, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1207860116.

MLA Handbook (7th Edition):

Hancock, James. “Organic Phase Entrapment of Glucose Oxidase In Polymeric Nanoparticles.” 2008. Web. 24 Jun 2019.

Vancouver:

Hancock J. Organic Phase Entrapment of Glucose Oxidase In Polymeric Nanoparticles. [Internet] [Masters thesis]. University of Akron; 2008. [cited 2019 Jun 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1207860116.

Council of Science Editors:

Hancock J. Organic Phase Entrapment of Glucose Oxidase In Polymeric Nanoparticles. [Masters Thesis]. University of Akron; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1207860116


Northeastern University

27. Rajarshi, Girija. The characterization of the human monoacylglycerol lipase using mutagenesis, enzyme kinetics and NMR spectroscopy.

Degree: PhD, Department of Pharmaceutical Sciences, 2017, Northeastern University

Subjects/Keywords: enzyme kinetics; enzymology; serine hydrolases

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APA (6th Edition):

Rajarshi, G. (2017). The characterization of the human monoacylglycerol lipase using mutagenesis, enzyme kinetics and NMR spectroscopy. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20284582

Chicago Manual of Style (16th Edition):

Rajarshi, Girija. “The characterization of the human monoacylglycerol lipase using mutagenesis, enzyme kinetics and NMR spectroscopy.” 2017. Doctoral Dissertation, Northeastern University. Accessed June 24, 2019. http://hdl.handle.net/2047/D20284582.

MLA Handbook (7th Edition):

Rajarshi, Girija. “The characterization of the human monoacylglycerol lipase using mutagenesis, enzyme kinetics and NMR spectroscopy.” 2017. Web. 24 Jun 2019.

Vancouver:

Rajarshi G. The characterization of the human monoacylglycerol lipase using mutagenesis, enzyme kinetics and NMR spectroscopy. [Internet] [Doctoral dissertation]. Northeastern University; 2017. [cited 2019 Jun 24]. Available from: http://hdl.handle.net/2047/D20284582.

Council of Science Editors:

Rajarshi G. The characterization of the human monoacylglycerol lipase using mutagenesis, enzyme kinetics and NMR spectroscopy. [Doctoral Dissertation]. Northeastern University; 2017. Available from: http://hdl.handle.net/2047/D20284582


Kennesaw State University

28. Rana, Hassan Ali. Isothermal Titration Calorimetry Uncovers Substrate Promiscuity of Bicupin Oxalate Oxidase.

Degree: MSCB, Chemistry, 2016, Kennesaw State University

  Oxalate oxidase from Ceriporiopsis subvermispora (CsOxOx) is a manganese-dependent enzyme that catalyzes the oxygen-dependent oxidation of oxalate to form two moles of carbon dioxide… (more)

Subjects/Keywords: oxalate oxidase; enzyme kinetics; isothermal titration calorimetry; Chemistry

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APA (6th Edition):

Rana, H. A. (2016). Isothermal Titration Calorimetry Uncovers Substrate Promiscuity of Bicupin Oxalate Oxidase. (Thesis). Kennesaw State University. Retrieved from https://digitalcommons.kennesaw.edu/mscs_etd/7

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):

Rana, Hassan Ali. “Isothermal Titration Calorimetry Uncovers Substrate Promiscuity of Bicupin Oxalate Oxidase.” 2016. Thesis, Kennesaw State University. Accessed June 24, 2019. https://digitalcommons.kennesaw.edu/mscs_etd/7.

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

MLA Handbook (7th Edition):

Rana, Hassan Ali. “Isothermal Titration Calorimetry Uncovers Substrate Promiscuity of Bicupin Oxalate Oxidase.” 2016. Web. 24 Jun 2019.

Vancouver:

Rana HA. Isothermal Titration Calorimetry Uncovers Substrate Promiscuity of Bicupin Oxalate Oxidase. [Internet] [Thesis]. Kennesaw State University; 2016. [cited 2019 Jun 24]. Available from: https://digitalcommons.kennesaw.edu/mscs_etd/7.

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

Council of Science Editors:

Rana HA. Isothermal Titration Calorimetry Uncovers Substrate Promiscuity of Bicupin Oxalate Oxidase. [Thesis]. Kennesaw State University; 2016. Available from: https://digitalcommons.kennesaw.edu/mscs_etd/7

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


University of Guelph

29. Poon, James. Hydrolysis of S-aryl-cysteinylglycine conjugates catalyzed by porcine kidney cortex membrane dipeptidase .

Degree: 2012, University of Guelph

 Following conjugation with glutathione, xenobiotics are converted into cysteinylglycine conjugates, cysteine conjugates, and, finally, mercapturic acids. The structural factors determining the activities of dipeptidases for… (more)

Subjects/Keywords: cilastatin; glutathione; mercapturic acid pathway; affinity chromatography; menaphthylglutathione; dinitrophenylglutathione; enzyme kinetics

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APA (6th Edition):

Poon, J. (2012). Hydrolysis of S-aryl-cysteinylglycine conjugates catalyzed by porcine kidney cortex membrane dipeptidase . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3897

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):

Poon, James. “Hydrolysis of S-aryl-cysteinylglycine conjugates catalyzed by porcine kidney cortex membrane dipeptidase .” 2012. Thesis, University of Guelph. Accessed June 24, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3897.

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

MLA Handbook (7th Edition):

Poon, James. “Hydrolysis of S-aryl-cysteinylglycine conjugates catalyzed by porcine kidney cortex membrane dipeptidase .” 2012. Web. 24 Jun 2019.

Vancouver:

Poon J. Hydrolysis of S-aryl-cysteinylglycine conjugates catalyzed by porcine kidney cortex membrane dipeptidase . [Internet] [Thesis]. University of Guelph; 2012. [cited 2019 Jun 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3897.

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

Council of Science Editors:

Poon J. Hydrolysis of S-aryl-cysteinylglycine conjugates catalyzed by porcine kidney cortex membrane dipeptidase . [Thesis]. University of Guelph; 2012. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3897

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


University of Guelph

30. Laderoute, Heidi. The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint .

Degree: 2015, University of Guelph

 Increased public interest in the welfare of pigs reared for pork production has led to an increased effort in finding new approaches for controlling the… (more)

Subjects/Keywords: Boar Taint; Androstenone; Sulfoconjugation; Sulfotransferase Enzymes; Glucuronidation; Enzyme Kinetics; Pig

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

APA (6th Edition):

Laderoute, H. (2015). The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837

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):

Laderoute, Heidi. “The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint .” 2015. Thesis, University of Guelph. Accessed June 24, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837.

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

MLA Handbook (7th Edition):

Laderoute, Heidi. “The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint .” 2015. Web. 24 Jun 2019.

Vancouver:

Laderoute H. The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint . [Internet] [Thesis]. University of Guelph; 2015. [cited 2019 Jun 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837.

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

Council of Science Editors:

Laderoute H. The metabolism of androstenone and other steroid hormone conjugates in relation to boar taint . [Thesis]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8837

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

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