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You searched for subject:(ENZYME BIOSYNTHESIS ENZYME ANABOLISM BIOCHEMISTRY ). Showing records 1 – 30 of 19779 total matches.

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University of Texas – Austin

1. -9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Biosynthetic studies of natural products are essential to the discovery and development of new drugs, because by understanding biosynthetic pathways and the enzymes that characterize… (more)

Subjects/Keywords: Biosynthesis; Aminoglycoside; Radical SAM; Enzyme

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APA (6th Edition):

-9265-9181. (2016). Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68375

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

Chicago Manual of Style (16th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed June 06, 2020. http://hdl.handle.net/2152/68375.

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

MLA Handbook (7th Edition):

-9265-9181. “Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides.” 2016. Web. 06 Jun 2020.

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

Vancouver:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2152/68375.

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

Council of Science Editors:

-9265-9181. Characterization of two radical S-adenosyl-L-methionine enzymes in the biosynthesis of aminoglycosides. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68375

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


University of Manchester

2. Lou, Xiao. BIOCHEMICAL AND STRUCTURAL STUDIES OF HUMAN METHIONINE SYNTHASE REDUCTASE.

Degree: 2010, University of Manchester

 ABSTRACTBIOCHEMICAL AND STRUCTURAL STUDIES OF HUMAN METHIONINE SYNTHASE REDUCTASE Human methionine synthase reductase (MSR) is a 78-kDa diflavin enzyme involved in folate and methionine metabolism.… (more)

Subjects/Keywords: biochemistry; enzyme; structure

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APA (6th Edition):

Lou, X. (2010). BIOCHEMICAL AND STRUCTURAL STUDIES OF HUMAN METHIONINE SYNTHASE REDUCTASE. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96429

Chicago Manual of Style (16th Edition):

Lou, Xiao. “BIOCHEMICAL AND STRUCTURAL STUDIES OF HUMAN METHIONINE SYNTHASE REDUCTASE.” 2010. Doctoral Dissertation, University of Manchester. Accessed June 06, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96429.

MLA Handbook (7th Edition):

Lou, Xiao. “BIOCHEMICAL AND STRUCTURAL STUDIES OF HUMAN METHIONINE SYNTHASE REDUCTASE.” 2010. Web. 06 Jun 2020.

Vancouver:

Lou X. BIOCHEMICAL AND STRUCTURAL STUDIES OF HUMAN METHIONINE SYNTHASE REDUCTASE. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2020 Jun 06]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96429.

Council of Science Editors:

Lou X. BIOCHEMICAL AND STRUCTURAL STUDIES OF HUMAN METHIONINE SYNTHASE REDUCTASE. [Doctoral Dissertation]. University of Manchester; 2010. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:96429


University of Manitoba

3. Hutchings, Roy. Probing the conformational dynamics of an OTU deubiquitinase enzyme active site.

Degree: Chemistry, 2016, University of Manitoba

 Enzymes are fundamental to cell function. Despite this, exactly how they work remains unclear. Enzymes exist as 3D folded structures determined by their amino acid… (more)

Subjects/Keywords: Biochemistry; Enzyme dynamics

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APA (6th Edition):

Hutchings, R. (2016). Probing the conformational dynamics of an OTU deubiquitinase enzyme active site. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31784

Chicago Manual of Style (16th Edition):

Hutchings, Roy. “Probing the conformational dynamics of an OTU deubiquitinase enzyme active site.” 2016. Masters Thesis, University of Manitoba. Accessed June 06, 2020. http://hdl.handle.net/1993/31784.

MLA Handbook (7th Edition):

Hutchings, Roy. “Probing the conformational dynamics of an OTU deubiquitinase enzyme active site.” 2016. Web. 06 Jun 2020.

Vancouver:

Hutchings R. Probing the conformational dynamics of an OTU deubiquitinase enzyme active site. [Internet] [Masters thesis]. University of Manitoba; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1993/31784.

Council of Science Editors:

Hutchings R. Probing the conformational dynamics of an OTU deubiquitinase enzyme active site. [Masters Thesis]. University of Manitoba; 2016. Available from: http://hdl.handle.net/1993/31784

4. Mayol, Ombeline. Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution.

Degree: Docteur es, Chimie, 2018, Université Paris-Saclay (ComUE)

L’importante représentation des amines chirales dans les molécules biologiquement actives a entrainé une forte dynamique de recherche autour de leur synthèse stéréosélective. A l’heure où… (more)

Subjects/Keywords: Enzyme

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APA (6th Edition):

Mayol, O. (2018). Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLE026

Chicago Manual of Style (16th Edition):

Mayol, Ombeline. “Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed June 06, 2020. http://www.theses.fr/2018SACLE026.

MLA Handbook (7th Edition):

Mayol, Ombeline. “Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution.” 2018. Web. 06 Jun 2020.

Vancouver:

Mayol O. Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Jun 06]. Available from: http://www.theses.fr/2018SACLE026.

Council of Science Editors:

Mayol O. Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLE026


University of Manchester

5. Lou, Xiao. Biochemical and structural studies of human methionine synthase reductase.

Degree: PhD, 2010, University of Manchester

 Human methionine synthase reductase (MSR) is a 78-kDa diflavin enzyme involved in folate and methionine metabolism. It regenerates the cofactor of methionine synthase (MS), cob(II),… (more)

Subjects/Keywords: 572.7; biochemistry, enzyme, structure

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APA (6th Edition):

Lou, X. (2010). Biochemical and structural studies of human methionine synthase reductase. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/biochemical-and-structural-studies-of-human-methionine-synthase-reductase(822952fc-8bef-4a30-9221-7fb154638193).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529220

Chicago Manual of Style (16th Edition):

Lou, Xiao. “Biochemical and structural studies of human methionine synthase reductase.” 2010. Doctoral Dissertation, University of Manchester. Accessed June 06, 2020. https://www.research.manchester.ac.uk/portal/en/theses/biochemical-and-structural-studies-of-human-methionine-synthase-reductase(822952fc-8bef-4a30-9221-7fb154638193).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529220.

MLA Handbook (7th Edition):

Lou, Xiao. “Biochemical and structural studies of human methionine synthase reductase.” 2010. Web. 06 Jun 2020.

Vancouver:

Lou X. Biochemical and structural studies of human methionine synthase reductase. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2020 Jun 06]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/biochemical-and-structural-studies-of-human-methionine-synthase-reductase(822952fc-8bef-4a30-9221-7fb154638193).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529220.

Council of Science Editors:

Lou X. Biochemical and structural studies of human methionine synthase reductase. [Doctoral Dissertation]. University of Manchester; 2010. Available from: https://www.research.manchester.ac.uk/portal/en/theses/biochemical-and-structural-studies-of-human-methionine-synthase-reductase(822952fc-8bef-4a30-9221-7fb154638193).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529220


Wilfrid Laurier University

6. 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 06, 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. 06 Jun 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 Jun 06]. 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


ETH Zürich

7. Bühler, Doris. Periplasmic proteins involved in the biogenesis of cytochrome oxidases in Bradyrhizobium japonicum.

Degree: 2010, ETH Zürich

Subjects/Keywords: BRADYRHIZOBIUM (MIKROBIOLOGIE); HÄM-GRUPPEN OXIDIERENDE OXYDOREDUKTASEN MIT SAUERSTOFF ALS AKZEPTOR, CYTOCHROMOXIDASEN (ENZYME); ENZYMBIOSYNTHESE + ENZYMANABOLISMUS (BIOCHEMIE); KUPFER UND KUPFERHALTIGE SUBSTANZEN (BIOCHEMIE); BRADYRHIZOBIUM (MICROBIOLOGY); HEME GROUP OXIDIZING OXIDOREDUCTASES WITH OXYGEN AS ACCEPTOR, CYTOCHROME OXIDASES (ENZYMES); ENZYME BIOSYNTHESIS + ENZYME ANABOLISM (BIOCHEMISTRY); COPPER AND COPPER CONTAINING COMPOUNDS (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Bühler, D. (2010). Periplasmic proteins involved in the biogenesis of cytochrome oxidases in Bradyrhizobium japonicum. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152500

Chicago Manual of Style (16th Edition):

Bühler, Doris. “Periplasmic proteins involved in the biogenesis of cytochrome oxidases in Bradyrhizobium japonicum.” 2010. Doctoral Dissertation, ETH Zürich. Accessed June 06, 2020. http://hdl.handle.net/20.500.11850/152500.

MLA Handbook (7th Edition):

Bühler, Doris. “Periplasmic proteins involved in the biogenesis of cytochrome oxidases in Bradyrhizobium japonicum.” 2010. Web. 06 Jun 2020.

Vancouver:

Bühler D. Periplasmic proteins involved in the biogenesis of cytochrome oxidases in Bradyrhizobium japonicum. [Internet] [Doctoral dissertation]. ETH Zürich; 2010. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/20.500.11850/152500.

Council of Science Editors:

Bühler D. Periplasmic proteins involved in the biogenesis of cytochrome oxidases in Bradyrhizobium japonicum. [Doctoral Dissertation]. ETH Zürich; 2010. Available from: http://hdl.handle.net/20.500.11850/152500


Iowa State University

8. Gray, Jennifer Ashley. Biotin biosynthetic enzymes and the metabolic control of biotin biosynthesis.

Degree: 2009, Iowa State University

 BIOTIN BIOSYNTHETIC ENZYMES AND THE METABOLIC CONTROL OF BIOTIN BIOSYNTHESIS Jennifer A. Gray and Basil J. Nikolau Biotin is a vital cofactor for many enzymes… (more)

Subjects/Keywords: Arabidopsis; biosynthesis; biotin; enzyme; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

Gray, J. A. (2009). Biotin biosynthetic enzymes and the metabolic control of biotin biosynthesis. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/11074

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):

Gray, Jennifer Ashley. “Biotin biosynthetic enzymes and the metabolic control of biotin biosynthesis.” 2009. Thesis, Iowa State University. Accessed June 06, 2020. https://lib.dr.iastate.edu/etd/11074.

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

MLA Handbook (7th Edition):

Gray, Jennifer Ashley. “Biotin biosynthetic enzymes and the metabolic control of biotin biosynthesis.” 2009. Web. 06 Jun 2020.

Vancouver:

Gray JA. Biotin biosynthetic enzymes and the metabolic control of biotin biosynthesis. [Internet] [Thesis]. Iowa State University; 2009. [cited 2020 Jun 06]. Available from: https://lib.dr.iastate.edu/etd/11074.

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

Council of Science Editors:

Gray JA. Biotin biosynthetic enzymes and the metabolic control of biotin biosynthesis. [Thesis]. Iowa State University; 2009. Available from: https://lib.dr.iastate.edu/etd/11074

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


ETH Zürich

9. Caravatti, Mario. Synthese und Degradation von Kreatinkinase-Untereinheiten während der Terminaldifferenzierung embryonaler Hühner-Skelettmuskelzellen in vitro.

Degree: 1979, ETH Zürich

Subjects/Keywords: KREATINKINASE (ENZYME); KATABOLISMUS, DISSIMILATION, BIOCHEMISCHER ABBAU (METABOLISMUS); ENZYMBIOSYNTHESE + ENZYMANABOLISMUS (BIOCHEMIE); MUSKELKRANKHEITEN + MUSKELBESCHWERDEN; EMBRYONALENTWICKLUNG (ZOOLOGIE); DIFFERENZIERUNG IN ZELLKOLONIEN UND ZELLPOPULATIONEN (CYTOLOGIE); CREATINE KINASE (ENZYMES); CATABOLISM, DISSIMILATION, DEGRADATION (METABOLISM); ENZYME BIOSYNTHESIS + ENZYME ANABOLISM (BIOCHEMISTRY); MUSCULAR DISEASES + MUSCULAR DISORDERS; EMBRYONIC DEVELOPMENT (ZOOLOGY); DIFFERENTIATION IN CELL POPULATIONS AND CELL COLONIES (CYTOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Caravatti, M. (1979). Synthese und Degradation von Kreatinkinase-Untereinheiten während der Terminaldifferenzierung embryonaler Hühner-Skelettmuskelzellen in vitro. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/136641

Chicago Manual of Style (16th Edition):

Caravatti, Mario. “Synthese und Degradation von Kreatinkinase-Untereinheiten während der Terminaldifferenzierung embryonaler Hühner-Skelettmuskelzellen in vitro.” 1979. Doctoral Dissertation, ETH Zürich. Accessed June 06, 2020. http://hdl.handle.net/20.500.11850/136641.

MLA Handbook (7th Edition):

Caravatti, Mario. “Synthese und Degradation von Kreatinkinase-Untereinheiten während der Terminaldifferenzierung embryonaler Hühner-Skelettmuskelzellen in vitro.” 1979. Web. 06 Jun 2020.

Vancouver:

Caravatti M. Synthese und Degradation von Kreatinkinase-Untereinheiten während der Terminaldifferenzierung embryonaler Hühner-Skelettmuskelzellen in vitro. [Internet] [Doctoral dissertation]. ETH Zürich; 1979. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/20.500.11850/136641.

Council of Science Editors:

Caravatti M. Synthese und Degradation von Kreatinkinase-Untereinheiten während der Terminaldifferenzierung embryonaler Hühner-Skelettmuskelzellen in vitro. [Doctoral Dissertation]. ETH Zürich; 1979. Available from: http://hdl.handle.net/20.500.11850/136641


ETH Zürich

10. Serventi, Fabio. Copper starvation-inducible protein for cytochrome oxidase biogenesis in Bradyrhizobium japonicum.

Degree: 2012, ETH Zürich

Subjects/Keywords: ENZYMBIOSYNTHESE + ENZYMANABOLISMUS (BIOCHEMIE); KUPFER (CHEMISCHE ELEMENTE); ENZYME BIOSYNTHESIS + ENZYME ANABOLISM (BIOCHEMISTRY); GENANALYSE (GENETISCHE TECHNIKEN); BRADYRHIZOBIUM (MIKROBIOLOGIE); OXIDASES (ENZYMES); GENE ANALYSIS (GENETIC TECHNIQUES); OXIDASEN (ENZYME); COPPER (CHEMICAL ELEMENTS); BRADYRHIZOBIUM (MICROBIOLOGY); info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/570; Life sciences; Life sciences

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APA (6th Edition):

Serventi, F. (2012). Copper starvation-inducible protein for cytochrome oxidase biogenesis in Bradyrhizobium japonicum. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/64960

Chicago Manual of Style (16th Edition):

Serventi, Fabio. “Copper starvation-inducible protein for cytochrome oxidase biogenesis in Bradyrhizobium japonicum.” 2012. Doctoral Dissertation, ETH Zürich. Accessed June 06, 2020. http://hdl.handle.net/20.500.11850/64960.

MLA Handbook (7th Edition):

Serventi, Fabio. “Copper starvation-inducible protein for cytochrome oxidase biogenesis in Bradyrhizobium japonicum.” 2012. Web. 06 Jun 2020.

Vancouver:

Serventi F. Copper starvation-inducible protein for cytochrome oxidase biogenesis in Bradyrhizobium japonicum. [Internet] [Doctoral dissertation]. ETH Zürich; 2012. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/20.500.11850/64960.

Council of Science Editors:

Serventi F. Copper starvation-inducible protein for cytochrome oxidase biogenesis in Bradyrhizobium japonicum. [Doctoral Dissertation]. ETH Zürich; 2012. Available from: http://hdl.handle.net/20.500.11850/64960


ETH Zürich

11. Beck, Gilles. Regulation of isoprenoid synthesis in Arabidopsis thaliana: Analysis of the GGPP branchpoint.

Degree: 2012, ETH Zürich

Subjects/Keywords: CHLOROPHYLLBIOSYNTHESE + CHLOROPHYLLANABOLISMUS (METABOLISMUS); ISOPRENOID BIOSYNTHESIS + ISOPRENOID ANABOLISM (METABOLISM); DIMETHYLALLYL-TRANS-TRANSFERASE (ENZYMES); ISOPRENOIDBIOSYNTHESE + ISOPRENOIDANABOLISMUS (METABOLISMUS); ISOENZYME (BIOCHEMIE); PHYLLOQUINONES, VITAMIN K1 (BIOCHEMISTRY); DIMETHYLALLYL-TRANS-TRANSFERASE (ENZYME); ARABIDOPSIS (BOTANY); MUTATIONEN + MUTANTEN (PFLANZENGENETIK); CAROTENOID BIOSYNTHESIS + CAROTENOID ANABOLISM (METABOLISM); PHYLLOCHINONE, VITAMIN-K1 (BIOCHEMIE); ARABIDOPSIS (BOTANIK); MUTATIONS + MUTANTS (PLANT GENETICS); CAROTINOIDBIOSYNTHESE + CAROTINOIDANABOLISMUS (METABOLISMUS); CHLOROPHYLL BIOSYNTHESIS + CHLOROPHYLL ANABOLISM (METABOLISM); ISOENZYMES (BIOCHEMISTRY); info:eu-repo/classification/ddc/570; info:eu-repo/classification/ddc/580; Life sciences; Botanical sciences

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APA (6th Edition):

Beck, G. (2012). Regulation of isoprenoid synthesis in Arabidopsis thaliana: Analysis of the GGPP branchpoint. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/65237

Chicago Manual of Style (16th Edition):

Beck, Gilles. “Regulation of isoprenoid synthesis in Arabidopsis thaliana: Analysis of the GGPP branchpoint.” 2012. Doctoral Dissertation, ETH Zürich. Accessed June 06, 2020. http://hdl.handle.net/20.500.11850/65237.

MLA Handbook (7th Edition):

Beck, Gilles. “Regulation of isoprenoid synthesis in Arabidopsis thaliana: Analysis of the GGPP branchpoint.” 2012. Web. 06 Jun 2020.

Vancouver:

Beck G. Regulation of isoprenoid synthesis in Arabidopsis thaliana: Analysis of the GGPP branchpoint. [Internet] [Doctoral dissertation]. ETH Zürich; 2012. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/20.500.11850/65237.

Council of Science Editors:

Beck G. Regulation of isoprenoid synthesis in Arabidopsis thaliana: Analysis of the GGPP branchpoint. [Doctoral Dissertation]. ETH Zürich; 2012. Available from: http://hdl.handle.net/20.500.11850/65237


University of Oxford

12. Murphy, Bonnie J. The importance of electron transfer in determining properties of [NiFe]-hydrogenases.

Degree: PhD, 2013, University of Oxford

 [NiFe] hydrogenases are microbial metalloenzymes that catalyse the reversible interconversion between molecular hydrogen and protons with high selectivity and efficiency. The catalytic properties of different… (more)

Subjects/Keywords: Biochemistry; enzyme catalysis; protein film electrochemistry; enzyme chemistry

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APA (6th Edition):

Murphy, B. J. (2013). The importance of electron transfer in determining properties of [NiFe]-hydrogenases. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:42258640-0fa6-4c48-a0f6-d6c8b9d7b3e0 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647550

Chicago Manual of Style (16th Edition):

Murphy, Bonnie J. “The importance of electron transfer in determining properties of [NiFe]-hydrogenases.” 2013. Doctoral Dissertation, University of Oxford. Accessed June 06, 2020. http://ora.ox.ac.uk/objects/uuid:42258640-0fa6-4c48-a0f6-d6c8b9d7b3e0 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647550.

MLA Handbook (7th Edition):

Murphy, Bonnie J. “The importance of electron transfer in determining properties of [NiFe]-hydrogenases.” 2013. Web. 06 Jun 2020.

Vancouver:

Murphy BJ. The importance of electron transfer in determining properties of [NiFe]-hydrogenases. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Jun 06]. Available from: http://ora.ox.ac.uk/objects/uuid:42258640-0fa6-4c48-a0f6-d6c8b9d7b3e0 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647550.

Council of Science Editors:

Murphy BJ. The importance of electron transfer in determining properties of [NiFe]-hydrogenases. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:42258640-0fa6-4c48-a0f6-d6c8b9d7b3e0 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647550


University of California – Santa Cruz

13. Hoobler, Eric Kerstan. Structural and Therapeutic Investigations of Human Lipoxygenase.

Degree: Chemistry, 2013, University of California – Santa Cruz

 The research in this dissertation describes the investigations of potential therapeutics as well as structural and allosteric properties of human lipoxygenases. Lipoxygenases (LOX) are a… (more)

Subjects/Keywords: Biochemistry; allosteric; enzyme; inhibitor; lipoxygenase; pseudoperoxidase; reductive

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APA (6th Edition):

Hoobler, E. K. (2013). Structural and Therapeutic Investigations of Human Lipoxygenase. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/34p7m3mg

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):

Hoobler, Eric Kerstan. “Structural and Therapeutic Investigations of Human Lipoxygenase.” 2013. Thesis, University of California – Santa Cruz. Accessed June 06, 2020. http://www.escholarship.org/uc/item/34p7m3mg.

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

MLA Handbook (7th Edition):

Hoobler, Eric Kerstan. “Structural and Therapeutic Investigations of Human Lipoxygenase.” 2013. Web. 06 Jun 2020.

Vancouver:

Hoobler EK. Structural and Therapeutic Investigations of Human Lipoxygenase. [Internet] [Thesis]. University of California – Santa Cruz; 2013. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/34p7m3mg.

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

Council of Science Editors:

Hoobler EK. Structural and Therapeutic Investigations of Human Lipoxygenase. [Thesis]. University of California – Santa Cruz; 2013. Available from: http://www.escholarship.org/uc/item/34p7m3mg

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


The Ohio State University

14. 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 06, 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. 06 Jun 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 Jun 06]. 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


Boston College

15. Martinez, Jessica. Monitoring Allosteric Effector Binding and Homotropic Cooperativity of Aspartate Transcarbamoylase.

Degree: MS, Chemistry, 2008, Boston College

 Aspartate transcarbamoylase (ATCase) catalyzes the reaction between carbamoyl phosphate (CP) and aspartate to form N-carbamoyl-L-aspartate (CA) and inorganic phosphate (Pi). In Escherichia coli, it catalyzes… (more)

Subjects/Keywords: biochemistry; enzyme; ATCase

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APA (6th Edition):

Martinez, J. (2008). Monitoring Allosteric Effector Binding and Homotropic Cooperativity of Aspartate Transcarbamoylase. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101353

Chicago Manual of Style (16th Edition):

Martinez, Jessica. “Monitoring Allosteric Effector Binding and Homotropic Cooperativity of Aspartate Transcarbamoylase.” 2008. Masters Thesis, Boston College. Accessed June 06, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101353.

MLA Handbook (7th Edition):

Martinez, Jessica. “Monitoring Allosteric Effector Binding and Homotropic Cooperativity of Aspartate Transcarbamoylase.” 2008. Web. 06 Jun 2020.

Vancouver:

Martinez J. Monitoring Allosteric Effector Binding and Homotropic Cooperativity of Aspartate Transcarbamoylase. [Internet] [Masters thesis]. Boston College; 2008. [cited 2020 Jun 06]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101353.

Council of Science Editors:

Martinez J. Monitoring Allosteric Effector Binding and Homotropic Cooperativity of Aspartate Transcarbamoylase. [Masters Thesis]. Boston College; 2008. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101353


University of Melbourne

16. EMANUELLE, SHANE. The regulation of SnRK1 from Arabidopsis thaliana.

Degree: 2013, University of Melbourne

 An intrinsic characteristic of all life is the ability to regulate the organism’s internal energy status despite sometimes wildly fluctuating conditions in the external environment.… (more)

Subjects/Keywords: SnRK1; SNF1; AMPK; enzyme; biochemistry; botany

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APA (6th Edition):

EMANUELLE, S. (2013). The regulation of SnRK1 from Arabidopsis thaliana. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38299

Chicago Manual of Style (16th Edition):

EMANUELLE, SHANE. “The regulation of SnRK1 from Arabidopsis thaliana.” 2013. Doctoral Dissertation, University of Melbourne. Accessed June 06, 2020. http://hdl.handle.net/11343/38299.

MLA Handbook (7th Edition):

EMANUELLE, SHANE. “The regulation of SnRK1 from Arabidopsis thaliana.” 2013. Web. 06 Jun 2020.

Vancouver:

EMANUELLE S. The regulation of SnRK1 from Arabidopsis thaliana. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/11343/38299.

Council of Science Editors:

EMANUELLE S. The regulation of SnRK1 from Arabidopsis thaliana. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38299


McMaster University

17. 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 06, 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. 06 Jun 2020.

Vancouver:

Balachandran N. DAHP Oxime: A Transition State Mimic Inhibitor Of DAHP Synthase. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2020 Jun 06]. 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


Princeton University

18. Schramma, Kelsey R. Discovery of a Family of Radical S-Adenosylmethionine Enzymes that Install a Novel Lysine-to-Tryptophan Crosslink .

Degree: PhD, 2017, Princeton University

 Nature has evolved a wide array of strategies for synthesizing bioactive secondary metabolites. One strategy involves ribosomal biosynthesis of a precursor peptide, which is then… (more)

Subjects/Keywords: Biosynthesis; Enzyme Mechanism; Natural Products; Peptides; Radical SAM; RiPP

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APA (6th Edition):

Schramma, K. R. (2017). Discovery of a Family of Radical S-Adenosylmethionine Enzymes that Install a Novel Lysine-to-Tryptophan Crosslink . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01gq67jt796

Chicago Manual of Style (16th Edition):

Schramma, Kelsey R. “Discovery of a Family of Radical S-Adenosylmethionine Enzymes that Install a Novel Lysine-to-Tryptophan Crosslink .” 2017. Doctoral Dissertation, Princeton University. Accessed June 06, 2020. http://arks.princeton.edu/ark:/88435/dsp01gq67jt796.

MLA Handbook (7th Edition):

Schramma, Kelsey R. “Discovery of a Family of Radical S-Adenosylmethionine Enzymes that Install a Novel Lysine-to-Tryptophan Crosslink .” 2017. Web. 06 Jun 2020.

Vancouver:

Schramma KR. Discovery of a Family of Radical S-Adenosylmethionine Enzymes that Install a Novel Lysine-to-Tryptophan Crosslink . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2020 Jun 06]. Available from: http://arks.princeton.edu/ark:/88435/dsp01gq67jt796.

Council of Science Editors:

Schramma KR. Discovery of a Family of Radical S-Adenosylmethionine Enzymes that Install a Novel Lysine-to-Tryptophan Crosslink . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp01gq67jt796


University of Texas – Austin

19. Thibodeaux, Christopher James. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.

Degree: PhD, Cell and Molecular Biology, 2010, University of Texas – Austin

 Enzymes are biological catalysts which greatly accelerate the rates of chemical reactions, oftentimes by many orders of magnitude over the uncatalyzed reaction. The remarkable catalytic… (more)

Subjects/Keywords: Enzyme catalysis; Isoprenoid biosynthesis; IDI-2; ACCD; Chemical mechanism

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APA (6th Edition):

Thibodeaux, C. J. (2010). Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22160

Chicago Manual of Style (16th Edition):

Thibodeaux, Christopher James. “Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed June 06, 2020. http://hdl.handle.net/2152/22160.

MLA Handbook (7th Edition):

Thibodeaux, Christopher James. “Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways.” 2010. Web. 06 Jun 2020.

Vancouver:

Thibodeaux CJ. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2152/22160.

Council of Science Editors:

Thibodeaux CJ. Mechanistic studies of two enzymes that employ common coenzymes in uncommon ways. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/22160


Simon Fraser University

20. Angus, Ronald H. Azasterol inhibition of [delta]24-sterol methyltransferase in yeast and its applications.

Degree: 1982, Simon Fraser University

Subjects/Keywords: Enzyme inhibitors.; Biosynthesis.; Sterols.; Yeast.

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APA (6th Edition):

Angus, R. H. (1982). Azasterol inhibition of [delta]24-sterol methyltransferase in yeast and its applications. (Thesis). Simon Fraser University. Retrieved from http://summit.sfu.ca/item/4047

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):

Angus, Ronald H. “Azasterol inhibition of [delta]24-sterol methyltransferase in yeast and its applications.” 1982. Thesis, Simon Fraser University. Accessed June 06, 2020. http://summit.sfu.ca/item/4047.

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

MLA Handbook (7th Edition):

Angus, Ronald H. “Azasterol inhibition of [delta]24-sterol methyltransferase in yeast and its applications.” 1982. Web. 06 Jun 2020.

Vancouver:

Angus RH. Azasterol inhibition of [delta]24-sterol methyltransferase in yeast and its applications. [Internet] [Thesis]. Simon Fraser University; 1982. [cited 2020 Jun 06]. Available from: http://summit.sfu.ca/item/4047.

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

Council of Science Editors:

Angus RH. Azasterol inhibition of [delta]24-sterol methyltransferase in yeast and its applications. [Thesis]. Simon Fraser University; 1982. Available from: http://summit.sfu.ca/item/4047

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


University of Texas – Austin

21. Lin, Geng-Min. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.

Degree: PhD, Chemistry, 2017, University of Texas – Austin

 Bacteria produce a great variety of unusual carbohydrates that are often found as parts of their cell surfaces or secondary metabolites. These components are crucial… (more)

Subjects/Keywords: Unusual carbohydrate; Biosynthesis; UDP-galactopyranose mutase; DesII; Radical SAM enzyme; Herbicidin

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APA (6th Edition):

Lin, G. (2017). Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/5870

Chicago Manual of Style (16th Edition):

Lin, Geng-Min. “Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed June 06, 2020. http://dx.doi.org/10.26153/tsw/5870.

MLA Handbook (7th Edition):

Lin, Geng-Min. “Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins.” 2017. Web. 06 Jun 2020.

Vancouver:

Lin G. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Jun 06]. Available from: http://dx.doi.org/10.26153/tsw/5870.

Council of Science Editors:

Lin G. Unusual carbohydrate biosynthesis : studies of the flavin-dependent isomerase UGM, the radical S-adenosyl-L-methionine enzyme DesII, and the biosynthesis of herbicidins. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/5870


University of Hawaii

22. Cramer, Julia Devine. (S)-Adenosyl-L-methionine and the Enzymes That Use it: Inhibition, Mutagenesis and Kinetic Studies from the Biotin Biosynthesis and Methionine Salvage Pathways.

Degree: 2019, University of Hawaii

Subjects/Keywords: Biochemistry; biotin biosynthesis; enzyme inhibition; enzyme kinetics; kinetic isotope effects; methionine salvage; radical SAM

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APA (6th Edition):

Cramer, J. D. (2019). (S)-Adenosyl-L-methionine and the Enzymes That Use it: Inhibition, Mutagenesis and Kinetic Studies from the Biotin Biosynthesis and Methionine Salvage Pathways. (Thesis). University of Hawaii. Retrieved from http://hdl.handle.net/10125/62255

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):

Cramer, Julia Devine. “(S)-Adenosyl-L-methionine and the Enzymes That Use it: Inhibition, Mutagenesis and Kinetic Studies from the Biotin Biosynthesis and Methionine Salvage Pathways.” 2019. Thesis, University of Hawaii. Accessed June 06, 2020. http://hdl.handle.net/10125/62255.

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

MLA Handbook (7th Edition):

Cramer, Julia Devine. “(S)-Adenosyl-L-methionine and the Enzymes That Use it: Inhibition, Mutagenesis and Kinetic Studies from the Biotin Biosynthesis and Methionine Salvage Pathways.” 2019. Web. 06 Jun 2020.

Vancouver:

Cramer JD. (S)-Adenosyl-L-methionine and the Enzymes That Use it: Inhibition, Mutagenesis and Kinetic Studies from the Biotin Biosynthesis and Methionine Salvage Pathways. [Internet] [Thesis]. University of Hawaii; 2019. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10125/62255.

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

Council of Science Editors:

Cramer JD. (S)-Adenosyl-L-methionine and the Enzymes That Use it: Inhibition, Mutagenesis and Kinetic Studies from the Biotin Biosynthesis and Methionine Salvage Pathways. [Thesis]. University of Hawaii; 2019. Available from: http://hdl.handle.net/10125/62255

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


University of Akron

23. 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 06, 2020. 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. 06 Jun 2020.

Vancouver:

Hancock J. Organic Phase Entrapment of Glucose Oxidase In Polymeric Nanoparticles. [Internet] [Masters thesis]. University of Akron; 2008. [cited 2020 Jun 06]. 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


University of California – Berkeley

24. Atreya, Meera Elizabeth. Engineering Cellulase Enzymes for Bioenergy.

Degree: Chemistry, 2015, University of California – Berkeley

 Sustainable energy sources, such as biofuels, offer increasingly important alternatives to fossil fuels that contribute less to global climate change. The energy contained within cellulosic… (more)

Subjects/Keywords: Biochemistry; Energy; Climate change; Biofuels; Cellulase; Directed Evolution; Enzyme; Enzyme Engineering; Product Inhibition

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APA (6th Edition):

Atreya, M. E. (2015). Engineering Cellulase Enzymes for Bioenergy. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6qm5p1mt

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):

Atreya, Meera Elizabeth. “Engineering Cellulase Enzymes for Bioenergy.” 2015. Thesis, University of California – Berkeley. Accessed June 06, 2020. http://www.escholarship.org/uc/item/6qm5p1mt.

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

MLA Handbook (7th Edition):

Atreya, Meera Elizabeth. “Engineering Cellulase Enzymes for Bioenergy.” 2015. Web. 06 Jun 2020.

Vancouver:

Atreya ME. Engineering Cellulase Enzymes for Bioenergy. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/6qm5p1mt.

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

Council of Science Editors:

Atreya ME. Engineering Cellulase Enzymes for Bioenergy. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/6qm5p1mt

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


Cornell University

25. O'Donnell, John P. Timing of Events, Reset Mechanism, and Allostery Innate to the GTP Hydrolysis Cycle of Atlastin .

Degree: 2017, Cornell University

 Homotypic membrane fusion of the smooth endoplasmic reticulum (ER) is catalyzed by atlastin (ATL), a member of the dynamin superfamily. Maintaining proper membrane architecture and… (more)

Subjects/Keywords: membrane fusion; allosteric regulation; dynamin-related proteins; enzyme mechanism; enzyme structure; GTPase; Biochemistry; Biophysics

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APA (6th Edition):

O'Donnell, J. P. (2017). Timing of Events, Reset Mechanism, and Allostery Innate to the GTP Hydrolysis Cycle of Atlastin . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59027

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):

O'Donnell, John P. “Timing of Events, Reset Mechanism, and Allostery Innate to the GTP Hydrolysis Cycle of Atlastin .” 2017. Thesis, Cornell University. Accessed June 06, 2020. http://hdl.handle.net/1813/59027.

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

MLA Handbook (7th Edition):

O'Donnell, John P. “Timing of Events, Reset Mechanism, and Allostery Innate to the GTP Hydrolysis Cycle of Atlastin .” 2017. Web. 06 Jun 2020.

Vancouver:

O'Donnell JP. Timing of Events, Reset Mechanism, and Allostery Innate to the GTP Hydrolysis Cycle of Atlastin . [Internet] [Thesis]. Cornell University; 2017. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1813/59027.

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

Council of Science Editors:

O'Donnell JP. Timing of Events, Reset Mechanism, and Allostery Innate to the GTP Hydrolysis Cycle of Atlastin . [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/59027

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

26. Jia, Feng. Design of novel nano-carriers for multi-enzyme co-localization.

Degree: 2013, Iowa State University

 The widely existing MECs in Nature have inspired researchers to design synthetic analogs to promote the overall catalytic efficiency in vitro by co-localizing multiple enzymes… (more)

Subjects/Keywords: Enzyme immobilization; Multi-enzyme co-localization; Nanoparticles; Nanotechnology; Polymers; Biochemistry; Chemical Engineering; Nanoscience and Nanotechnology

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APA (6th Edition):

Jia, F. (2013). Design of novel nano-carriers for multi-enzyme co-localization. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/13378

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):

Jia, Feng. “Design of novel nano-carriers for multi-enzyme co-localization.” 2013. Thesis, Iowa State University. Accessed June 06, 2020. https://lib.dr.iastate.edu/etd/13378.

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

MLA Handbook (7th Edition):

Jia, Feng. “Design of novel nano-carriers for multi-enzyme co-localization.” 2013. Web. 06 Jun 2020.

Vancouver:

Jia F. Design of novel nano-carriers for multi-enzyme co-localization. [Internet] [Thesis]. Iowa State University; 2013. [cited 2020 Jun 06]. Available from: https://lib.dr.iastate.edu/etd/13378.

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

Council of Science Editors:

Jia F. Design of novel nano-carriers for multi-enzyme co-localization. [Thesis]. Iowa State University; 2013. Available from: https://lib.dr.iastate.edu/etd/13378

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


ETH Zürich

27. Hirsch, Anna Katharina Herta. A novel approach towards antimalarials: design and synthesis of inhibitors of the kinase IspE.

Degree: 2008, ETH Zürich

Subjects/Keywords: PHOSPHOTRANSFERASEN (ENZYME); ISOPRENOIDBIOSYNTHESE + ISOPRENOIDANABOLISMUS (METABOLISMUS); INHIBITOREN (KATALYSE); PHOSPHOTRANSFERASES (ENZYMES); ISOPRENOID BIOSYNTHESIS + ISOPRENOID ANABOLISM (METABOLISM); INHIBITORS (CATALYSIS); info:eu-repo/classification/ddc/570; Life sciences

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

APA (6th Edition):

Hirsch, A. K. H. (2008). A novel approach towards antimalarials: design and synthesis of inhibitors of the kinase IspE. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/150595

Chicago Manual of Style (16th Edition):

Hirsch, Anna Katharina Herta. “A novel approach towards antimalarials: design and synthesis of inhibitors of the kinase IspE.” 2008. Doctoral Dissertation, ETH Zürich. Accessed June 06, 2020. http://hdl.handle.net/20.500.11850/150595.

MLA Handbook (7th Edition):

Hirsch, Anna Katharina Herta. “A novel approach towards antimalarials: design and synthesis of inhibitors of the kinase IspE.” 2008. Web. 06 Jun 2020.

Vancouver:

Hirsch AKH. A novel approach towards antimalarials: design and synthesis of inhibitors of the kinase IspE. [Internet] [Doctoral dissertation]. ETH Zürich; 2008. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/20.500.11850/150595.

Council of Science Editors:

Hirsch AKH. A novel approach towards antimalarials: design and synthesis of inhibitors of the kinase IspE. [Doctoral Dissertation]. ETH Zürich; 2008. Available from: http://hdl.handle.net/20.500.11850/150595


University of Michigan

28. Ding, Yousong. Characterization and Analysis of Biosynthetic Systems from Nostoc sp. ATCC 53789 and Selected Fungal Natural Product Pathways.

Degree: PhD, Medicinal Chemistry, 2010, University of Michigan

 Complex secondary metabolites display diverse biological activities and together with their derivatives have provided over two-thirds of new pharmaceutical agents introduced during the past two… (more)

Subjects/Keywords: Natural Product; Biosynthesis; Chemoenzymatic Synthesis; Genome Mining; Enzyme Characterization; Biological Chemistry; Science

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

APA (6th Edition):

Ding, Y. (2010). Characterization and Analysis of Biosynthetic Systems from Nostoc sp. ATCC 53789 and Selected Fungal Natural Product Pathways. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/76020

Chicago Manual of Style (16th Edition):

Ding, Yousong. “Characterization and Analysis of Biosynthetic Systems from Nostoc sp. ATCC 53789 and Selected Fungal Natural Product Pathways.” 2010. Doctoral Dissertation, University of Michigan. Accessed June 06, 2020. http://hdl.handle.net/2027.42/76020.

MLA Handbook (7th Edition):

Ding, Yousong. “Characterization and Analysis of Biosynthetic Systems from Nostoc sp. ATCC 53789 and Selected Fungal Natural Product Pathways.” 2010. Web. 06 Jun 2020.

Vancouver:

Ding Y. Characterization and Analysis of Biosynthetic Systems from Nostoc sp. ATCC 53789 and Selected Fungal Natural Product Pathways. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2027.42/76020.

Council of Science Editors:

Ding Y. Characterization and Analysis of Biosynthetic Systems from Nostoc sp. ATCC 53789 and Selected Fungal Natural Product Pathways. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/76020


University of Technology, Sydney

29. Kasz, Robert. Investigating DHCR24 as a protector against cellular stress : more than just a cholesterol-synthesising enzyme.

Degree: 2017, University of Technology, Sydney

 Atherosclerosis and insulin resistance are globally prevalent metabolic diseases, primarily driven by endothelial and hepatic inflammation, respectively. High density lipoprotein (HDL) reduces the inflammation in… (more)

Subjects/Keywords: Atherosclerosis.; Insulin resistance.; Cholesterol biosynthesis enzyme DHCR24; High density lipoprotein (HDL); HCAECs and HuH7 cells.

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

APA (6th Edition):

Kasz, R. (2017). Investigating DHCR24 as a protector against cellular stress : more than just a cholesterol-synthesising enzyme. (Thesis). University of Technology, Sydney. Retrieved from http://hdl.handle.net/10453/90267

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):

Kasz, Robert. “Investigating DHCR24 as a protector against cellular stress : more than just a cholesterol-synthesising enzyme.” 2017. Thesis, University of Technology, Sydney. Accessed June 06, 2020. http://hdl.handle.net/10453/90267.

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

MLA Handbook (7th Edition):

Kasz, Robert. “Investigating DHCR24 as a protector against cellular stress : more than just a cholesterol-synthesising enzyme.” 2017. Web. 06 Jun 2020.

Vancouver:

Kasz R. Investigating DHCR24 as a protector against cellular stress : more than just a cholesterol-synthesising enzyme. [Internet] [Thesis]. University of Technology, Sydney; 2017. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/10453/90267.

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

Council of Science Editors:

Kasz R. Investigating DHCR24 as a protector against cellular stress : more than just a cholesterol-synthesising enzyme. [Thesis]. University of Technology, Sydney; 2017. Available from: http://hdl.handle.net/10453/90267

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


University of Illinois – Urbana-Champaign

30. Peck, Spencer. Mechanistic investigations of enzymes in phosphonate metabolism.

Degree: PhD, 0335, 2015, University of Illinois – Urbana-Champaign

 Synthetic and naturally-occurring phosphonates have found widespread use in both agriculture and medicine. A program at the Institute for Genomic Biology at the University of… (more)

Subjects/Keywords: Phosphonate biosynthesis; enzymology; non-heme iron-dependent enzyme; 2-Hydroxyethylphosphonate dioxygenase (HEPD); methylphosphonate synthase (MPnS)

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

APA (6th Edition):

Peck, S. (2015). Mechanistic investigations of enzymes in phosphonate metabolism. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/73062

Chicago Manual of Style (16th Edition):

Peck, Spencer. “Mechanistic investigations of enzymes in phosphonate metabolism.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed June 06, 2020. http://hdl.handle.net/2142/73062.

MLA Handbook (7th Edition):

Peck, Spencer. “Mechanistic investigations of enzymes in phosphonate metabolism.” 2015. Web. 06 Jun 2020.

Vancouver:

Peck S. Mechanistic investigations of enzymes in phosphonate metabolism. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2142/73062.

Council of Science Editors:

Peck S. Mechanistic investigations of enzymes in phosphonate metabolism. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/73062

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