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Degree: PhD

You searched for subject:(ribose 5 phosphate isomerase). Showing records 1 – 30 of 735 total matches.

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1. Cech, David. Insights into the Mechanistic and Regulatory Properties of D-arabinose-5-phosphate.

Degree: PhD, Medicinal Chemistry, 2017, University of Michigan

 Arabinose-5-phosphate isomerase (API) catalyzes the interconversion of D-ribulose-5-phosphate and D-arabinose-5-phosphate (A5P), which is the first step in the biosynthesis of 3-deoxy-D-manno-octulosonate (Kdo). Kdo, an important… (more)

Subjects/Keywords: D-arabinose-5-phosphate isomerase; D-arabinose-5-phosphate; Biological Chemistry; Science

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APA (6th Edition):

Cech, D. (2017). Insights into the Mechanistic and Regulatory Properties of D-arabinose-5-phosphate. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/138618

Chicago Manual of Style (16th Edition):

Cech, David. “Insights into the Mechanistic and Regulatory Properties of D-arabinose-5-phosphate.” 2017. Doctoral Dissertation, University of Michigan. Accessed July 22, 2019. http://hdl.handle.net/2027.42/138618.

MLA Handbook (7th Edition):

Cech, David. “Insights into the Mechanistic and Regulatory Properties of D-arabinose-5-phosphate.” 2017. Web. 22 Jul 2019.

Vancouver:

Cech D. Insights into the Mechanistic and Regulatory Properties of D-arabinose-5-phosphate. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2027.42/138618.

Council of Science Editors:

Cech D. Insights into the Mechanistic and Regulatory Properties of D-arabinose-5-phosphate. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/138618


University of Georgia

2. Lima, Santiago. Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes.

Degree: PhD, Biochemistry and Molecular Biology, 2008, University of Georgia

 Pyridoxal-5’-phosphate (PLP) dependent enzymes are a large and catalytically diversegroup of proteins primarily involved in the metabolism of amino acids, amino acid derived compounds, and… (more)

Subjects/Keywords: pyridoxal-5'-phosphate

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APA (6th Edition):

Lima, S. (2008). Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/lima_santiago_200805_phd

Chicago Manual of Style (16th Edition):

Lima, Santiago. “Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes.” 2008. Doctoral Dissertation, University of Georgia. Accessed July 22, 2019. http://purl.galileo.usg.edu/uga_etd/lima_santiago_200805_phd.

MLA Handbook (7th Edition):

Lima, Santiago. “Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes.” 2008. Web. 22 Jul 2019.

Vancouver:

Lima S. Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes. [Internet] [Doctoral dissertation]. University of Georgia; 2008. [cited 2019 Jul 22]. Available from: http://purl.galileo.usg.edu/uga_etd/lima_santiago_200805_phd.

Council of Science Editors:

Lima S. Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes. [Doctoral Dissertation]. University of Georgia; 2008. Available from: http://purl.galileo.usg.edu/uga_etd/lima_santiago_200805_phd


University of Exeter

3. Abdulla, Sheera. Biochemical characterisation of unusual glycolytic enzymes from the human intestinal parasite Blastocystis hominis.

Degree: PhD, 2016, University of Exeter

 Blastocystis is an important parasite that infects humans and a wide range of animals like rats, birds, reptiles, etc. infecting a sum of 60% of… (more)

Subjects/Keywords: 572.8; Blastocystis; Stramenopile; triosephosphate isomerase-glyceraldehyde-3-phosphate dehydrogenase(TPI-GAPDH); enolase

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APA (6th Edition):

Abdulla, S. (2016). Biochemical characterisation of unusual glycolytic enzymes from the human intestinal parasite Blastocystis hominis. (Doctoral Dissertation). University of Exeter. Retrieved from http://hdl.handle.net/10871/23933

Chicago Manual of Style (16th Edition):

Abdulla, Sheera. “Biochemical characterisation of unusual glycolytic enzymes from the human intestinal parasite Blastocystis hominis.” 2016. Doctoral Dissertation, University of Exeter. Accessed July 22, 2019. http://hdl.handle.net/10871/23933.

MLA Handbook (7th Edition):

Abdulla, Sheera. “Biochemical characterisation of unusual glycolytic enzymes from the human intestinal parasite Blastocystis hominis.” 2016. Web. 22 Jul 2019.

Vancouver:

Abdulla S. Biochemical characterisation of unusual glycolytic enzymes from the human intestinal parasite Blastocystis hominis. [Internet] [Doctoral dissertation]. University of Exeter; 2016. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10871/23933.

Council of Science Editors:

Abdulla S. Biochemical characterisation of unusual glycolytic enzymes from the human intestinal parasite Blastocystis hominis. [Doctoral Dissertation]. University of Exeter; 2016. Available from: http://hdl.handle.net/10871/23933


Texas A&M University

4. Eltahan, Rana Abbas Khedr. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.

Degree: PhD, Biomedical Sciences, 2018, Texas A&M University

 Cryptosporidium parvum is a water-borne and food-borne apicomplexan pathogen. It is one of the top four diarrheal-causing pathogens in children under the age of five… (more)

Subjects/Keywords: : Apicomplexan; Cryptosporidium parvum; Glucose-6-phosphate isomerase (GPI); Ebselen; Hexokinase (HK): Drug target

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APA (6th Edition):

Eltahan, R. A. K. (2018). Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173649

Chicago Manual of Style (16th Edition):

Eltahan, Rana Abbas Khedr. “Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.” 2018. Doctoral Dissertation, Texas A&M University. Accessed July 22, 2019. http://hdl.handle.net/1969.1/173649.

MLA Handbook (7th Edition):

Eltahan, Rana Abbas Khedr. “Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.” 2018. Web. 22 Jul 2019.

Vancouver:

Eltahan RAK. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/1969.1/173649.

Council of Science Editors:

Eltahan RAK. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173649

5. Cordeiro, Artur Torres. Determinação da estrutura cristalográfica da enzima glicose-6-fosfato isomerase de Leishmania mexicana e comparação com a enzima homóloga de humanos.

Degree: PhD, Física Aplicada, 2004, University of São Paulo

Esta tese apresenta em sua introdução uma revisão bibliográfica sobre a leishmaniose no Brasil e no mundo, com dados atuais de documentos do Ministério da… (more)

Subjects/Keywords: Crystallographic structure; Estrutura cristalográfica; Glicose-6-fosfato; Glicose-6-phosphate; Isomerase; Isomerase; Leishmania

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APA (6th Edition):

Cordeiro, A. T. (2004). Determinação da estrutura cristalográfica da enzima glicose-6-fosfato isomerase de Leishmania mexicana e comparação com a enzima homóloga de humanos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/76/76132/tde-09042008-100756/ ;

Chicago Manual of Style (16th Edition):

Cordeiro, Artur Torres. “Determinação da estrutura cristalográfica da enzima glicose-6-fosfato isomerase de Leishmania mexicana e comparação com a enzima homóloga de humanos.” 2004. Doctoral Dissertation, University of São Paulo. Accessed July 22, 2019. http://www.teses.usp.br/teses/disponiveis/76/76132/tde-09042008-100756/ ;.

MLA Handbook (7th Edition):

Cordeiro, Artur Torres. “Determinação da estrutura cristalográfica da enzima glicose-6-fosfato isomerase de Leishmania mexicana e comparação com a enzima homóloga de humanos.” 2004. Web. 22 Jul 2019.

Vancouver:

Cordeiro AT. Determinação da estrutura cristalográfica da enzima glicose-6-fosfato isomerase de Leishmania mexicana e comparação com a enzima homóloga de humanos. [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2019 Jul 22]. Available from: http://www.teses.usp.br/teses/disponiveis/76/76132/tde-09042008-100756/ ;.

Council of Science Editors:

Cordeiro AT. Determinação da estrutura cristalográfica da enzima glicose-6-fosfato isomerase de Leishmania mexicana e comparação com a enzima homóloga de humanos. [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/76/76132/tde-09042008-100756/ ;


University of Alberta

6. Fan, Chenguang. Structural and Inhibitory Studies of LL-Diaminopimelate Aminotransferase and Investigation of Methods for Small Peptide Crystallization.

Degree: PhD, Department of Chemistry, 2012, University of Alberta

 The pyridoxal-5'-phosphate (PLP)-dependent enzyme LL-diaminopimelate aminotransferase (LL-DAP-AT) catalyzes a key step in the biosynthesis of L-lysine in plants and Chlamydia. In this thesis, studies of… (more)

Subjects/Keywords: LL-Diaminopimelate Aminotransferase; pyridoxal-5'-phosphate; Subtilosin A

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APA (6th Edition):

Fan, C. (2012). Structural and Inhibitory Studies of LL-Diaminopimelate Aminotransferase and Investigation of Methods for Small Peptide Crystallization. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cz30pt76c

Chicago Manual of Style (16th Edition):

Fan, Chenguang. “Structural and Inhibitory Studies of LL-Diaminopimelate Aminotransferase and Investigation of Methods for Small Peptide Crystallization.” 2012. Doctoral Dissertation, University of Alberta. Accessed July 22, 2019. https://era.library.ualberta.ca/files/cz30pt76c.

MLA Handbook (7th Edition):

Fan, Chenguang. “Structural and Inhibitory Studies of LL-Diaminopimelate Aminotransferase and Investigation of Methods for Small Peptide Crystallization.” 2012. Web. 22 Jul 2019.

Vancouver:

Fan C. Structural and Inhibitory Studies of LL-Diaminopimelate Aminotransferase and Investigation of Methods for Small Peptide Crystallization. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2019 Jul 22]. Available from: https://era.library.ualberta.ca/files/cz30pt76c.

Council of Science Editors:

Fan C. Structural and Inhibitory Studies of LL-Diaminopimelate Aminotransferase and Investigation of Methods for Small Peptide Crystallization. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/cz30pt76c


University of Georgia

7. Ernst, Dustin Casey. Exploring sources and metabolic consequences of 2-aminoacrylate stress in bacteria and yeast.

Degree: PhD, Microbiology, 2017, University of Georgia

 Reactive metabolites are produced by many biochemical pathways within a given metabolic network. The inherent reactivity of these metabolites presents a challenge to cells, where… (more)

Subjects/Keywords: Enamine; 2-aminoacrylate; Metabolic stress; Pyridoxal 5’-phosphate; RidA

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APA (6th Edition):

Ernst, D. C. (2017). Exploring sources and metabolic consequences of 2-aminoacrylate stress in bacteria and yeast. (Doctoral Dissertation). University of Georgia. Retrieved from http://hdl.handle.net/10724/37728

Chicago Manual of Style (16th Edition):

Ernst, Dustin Casey. “Exploring sources and metabolic consequences of 2-aminoacrylate stress in bacteria and yeast.” 2017. Doctoral Dissertation, University of Georgia. Accessed July 22, 2019. http://hdl.handle.net/10724/37728.

MLA Handbook (7th Edition):

Ernst, Dustin Casey. “Exploring sources and metabolic consequences of 2-aminoacrylate stress in bacteria and yeast.” 2017. Web. 22 Jul 2019.

Vancouver:

Ernst DC. Exploring sources and metabolic consequences of 2-aminoacrylate stress in bacteria and yeast. [Internet] [Doctoral dissertation]. University of Georgia; 2017. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10724/37728.

Council of Science Editors:

Ernst DC. Exploring sources and metabolic consequences of 2-aminoacrylate stress in bacteria and yeast. [Doctoral Dissertation]. University of Georgia; 2017. Available from: http://hdl.handle.net/10724/37728


Virginia Tech

8. Sun, Furong. Structural basis for interactions of the Phytophthora sojae RxLR effector Avh5 with phosphatidylinositol 3-phosphate and for host cell entry.

Degree: PhD, Chemistry, 2012, Virginia Tech

 Oomycetes, such as Phytophthora sojae, are plant pathogens that employ protein effectors that enter host cells to facilitate infection. Plants may overcome infection by recognizing… (more)

Subjects/Keywords: Phytophthora sojae; Protein-lipid interactions; Phosphatidylinositol 3-phosphate; Avirulence homolog-5

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APA (6th Edition):

Sun, F. (2012). Structural basis for interactions of the Phytophthora sojae RxLR effector Avh5 with phosphatidylinositol 3-phosphate and for host cell entry. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/37657

Chicago Manual of Style (16th Edition):

Sun, Furong. “Structural basis for interactions of the Phytophthora sojae RxLR effector Avh5 with phosphatidylinositol 3-phosphate and for host cell entry.” 2012. Doctoral Dissertation, Virginia Tech. Accessed July 22, 2019. http://hdl.handle.net/10919/37657.

MLA Handbook (7th Edition):

Sun, Furong. “Structural basis for interactions of the Phytophthora sojae RxLR effector Avh5 with phosphatidylinositol 3-phosphate and for host cell entry.” 2012. Web. 22 Jul 2019.

Vancouver:

Sun F. Structural basis for interactions of the Phytophthora sojae RxLR effector Avh5 with phosphatidylinositol 3-phosphate and for host cell entry. [Internet] [Doctoral dissertation]. Virginia Tech; 2012. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10919/37657.

Council of Science Editors:

Sun F. Structural basis for interactions of the Phytophthora sojae RxLR effector Avh5 with phosphatidylinositol 3-phosphate and for host cell entry. [Doctoral Dissertation]. Virginia Tech; 2012. Available from: http://hdl.handle.net/10919/37657


University of Illinois – Urbana-Champaign

9. Sobota, Jason. Identification and characterization of a novel class of hydrogen peroxide targets in escherichia coli.

Degree: PhD, 0322, 2014, University of Illinois – Urbana-Champaign

 In nature, microorganisms are constantly exposed to micromolar levels of hydrogen peroxide (H2O2) from sources such as host defenses or byproducts of chemical processes. This… (more)

Subjects/Keywords: hydrogen peroxide; mononuclear iron enzymes; oxidative stress; ribulose 5-phosphate 3-epimerase (Rpe); 3-Deoxy-D-arabinoheptulosonate 7-phosphate (DAHP) synthase

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APA (6th Edition):

Sobota, J. (2014). Identification and characterization of a novel class of hydrogen peroxide targets in escherichia coli. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49673

Chicago Manual of Style (16th Edition):

Sobota, Jason. “Identification and characterization of a novel class of hydrogen peroxide targets in escherichia coli.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/49673.

MLA Handbook (7th Edition):

Sobota, Jason. “Identification and characterization of a novel class of hydrogen peroxide targets in escherichia coli.” 2014. Web. 22 Jul 2019.

Vancouver:

Sobota J. Identification and characterization of a novel class of hydrogen peroxide targets in escherichia coli. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/49673.

Council of Science Editors:

Sobota J. Identification and characterization of a novel class of hydrogen peroxide targets in escherichia coli. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49673


University of Alberta

10. Watanabe, Nobuhiko. LL-diaminopimelate aminotransferase: the mechanism of substrate recognition and specificity.

Degree: PhD, Department of Biochemistry, 2010, University of Alberta

 Amino acid biosynthesis is an essential process in living organisms. Certain amino acids can be synthesized by some organisms but not by others. L-Lysine is… (more)

Subjects/Keywords: Chlamydia trachomatis; Lysine biosynthesis; Pyridoxal 5'-phosphate; LL-diaminopimelate aminotransferase; Arabidopsis thaliana

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APA (6th Edition):

Watanabe, N. (2010). LL-diaminopimelate aminotransferase: the mechanism of substrate recognition and specificity. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/6682x498k

Chicago Manual of Style (16th Edition):

Watanabe, Nobuhiko. “LL-diaminopimelate aminotransferase: the mechanism of substrate recognition and specificity.” 2010. Doctoral Dissertation, University of Alberta. Accessed July 22, 2019. https://era.library.ualberta.ca/files/6682x498k.

MLA Handbook (7th Edition):

Watanabe, Nobuhiko. “LL-diaminopimelate aminotransferase: the mechanism of substrate recognition and specificity.” 2010. Web. 22 Jul 2019.

Vancouver:

Watanabe N. LL-diaminopimelate aminotransferase: the mechanism of substrate recognition and specificity. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2019 Jul 22]. Available from: https://era.library.ualberta.ca/files/6682x498k.

Council of Science Editors:

Watanabe N. LL-diaminopimelate aminotransferase: the mechanism of substrate recognition and specificity. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/6682x498k


University of Manchester

11. Grainger, Deborah. Investigation of phosphatidylinositol 5-phosphate's role in insulin-stimulated glucose uptake in a skeletal muscle cell line.

Degree: PhD, 2011, University of Manchester

 Phosphatidylinositol 5-phosphate (PtdIns5P) is the least well-characterised member of the phosphoinositide family of essential regulatory phospholipids. PtdIns5P levels are altered within cells in response to… (more)

Subjects/Keywords: skeletal muscle cell line; L6; phosphatidylinositol 5-phosphate; PtdIns5P; Insulin; GLUT4; Glucose uptake

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APA (6th Edition):

Grainger, D. (2011). Investigation of phosphatidylinositol 5-phosphate's role in insulin-stimulated glucose uptake in a skeletal muscle cell line. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-phosphatidylinositol-5phosphates-role-in-insulinstimulated-glucose-uptake-in-a-skeletal-muscle-cell-line(76a69150-5434-43e4-a961-b629518bd931).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740238

Chicago Manual of Style (16th Edition):

Grainger, Deborah. “Investigation of phosphatidylinositol 5-phosphate's role in insulin-stimulated glucose uptake in a skeletal muscle cell line.” 2011. Doctoral Dissertation, University of Manchester. Accessed July 22, 2019. https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-phosphatidylinositol-5phosphates-role-in-insulinstimulated-glucose-uptake-in-a-skeletal-muscle-cell-line(76a69150-5434-43e4-a961-b629518bd931).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740238.

MLA Handbook (7th Edition):

Grainger, Deborah. “Investigation of phosphatidylinositol 5-phosphate's role in insulin-stimulated glucose uptake in a skeletal muscle cell line.” 2011. Web. 22 Jul 2019.

Vancouver:

Grainger D. Investigation of phosphatidylinositol 5-phosphate's role in insulin-stimulated glucose uptake in a skeletal muscle cell line. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2019 Jul 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-phosphatidylinositol-5phosphates-role-in-insulinstimulated-glucose-uptake-in-a-skeletal-muscle-cell-line(76a69150-5434-43e4-a961-b629518bd931).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740238.

Council of Science Editors:

Grainger D. Investigation of phosphatidylinositol 5-phosphate's role in insulin-stimulated glucose uptake in a skeletal muscle cell line. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-phosphatidylinositol-5phosphates-role-in-insulinstimulated-glucose-uptake-in-a-skeletal-muscle-cell-line(76a69150-5434-43e4-a961-b629518bd931).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740238


Virginia Tech

12. Liu, Pingyang. Biochemical studies of enzymes in insect cuticle hardening.

Degree: PhD, Biochemistry, 2013, Virginia Tech

 In insects, the cuticle provides protection against physical injury and water loss, rigidness for muscle attachment and mechanical support, and flexibility in inter-segmental and joint… (more)

Subjects/Keywords: aspartate 1-decarboxylase; pyridoxal 5-phosphate; cysteine sulfinic acid; taurine; hypotaurine; beta-alanine; cysteine; glutamat

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APA (6th Edition):

Liu, P. (2013). Biochemical studies of enzymes in insect cuticle hardening. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/50528

Chicago Manual of Style (16th Edition):

Liu, Pingyang. “Biochemical studies of enzymes in insect cuticle hardening.” 2013. Doctoral Dissertation, Virginia Tech. Accessed July 22, 2019. http://hdl.handle.net/10919/50528.

MLA Handbook (7th Edition):

Liu, Pingyang. “Biochemical studies of enzymes in insect cuticle hardening.” 2013. Web. 22 Jul 2019.

Vancouver:

Liu P. Biochemical studies of enzymes in insect cuticle hardening. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10919/50528.

Council of Science Editors:

Liu P. Biochemical studies of enzymes in insect cuticle hardening. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/50528


University of Wisconsin – Milwaukee

13. Han, Lanlan. Structure-Function Relationships in Bacterial Regulatory Proteins and an Enzyme Involved in Antibiotic Biosynthesis.

Degree: PhD, Chemistry, 2017, University of Wisconsin – Milwaukee

  The first part of my thesis is focused on a new family of two-component response regulator proteins: Aspartate-Less Regulators (ALR). They lack the catalytic… (more)

Subjects/Keywords: Antibiotic Biosynthesis; Aspartate-Less Regulators; Enduracididine; Oxidase; Pyridoxal-5’-Phosphate; Redox Sensor; Biochemistry

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APA (6th Edition):

Han, L. (2017). Structure-Function Relationships in Bacterial Regulatory Proteins and an Enzyme Involved in Antibiotic Biosynthesis. (Doctoral Dissertation). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/1636

Chicago Manual of Style (16th Edition):

Han, Lanlan. “Structure-Function Relationships in Bacterial Regulatory Proteins and an Enzyme Involved in Antibiotic Biosynthesis.” 2017. Doctoral Dissertation, University of Wisconsin – Milwaukee. Accessed July 22, 2019. https://dc.uwm.edu/etd/1636.

MLA Handbook (7th Edition):

Han, Lanlan. “Structure-Function Relationships in Bacterial Regulatory Proteins and an Enzyme Involved in Antibiotic Biosynthesis.” 2017. Web. 22 Jul 2019.

Vancouver:

Han L. Structure-Function Relationships in Bacterial Regulatory Proteins and an Enzyme Involved in Antibiotic Biosynthesis. [Internet] [Doctoral dissertation]. University of Wisconsin – Milwaukee; 2017. [cited 2019 Jul 22]. Available from: https://dc.uwm.edu/etd/1636.

Council of Science Editors:

Han L. Structure-Function Relationships in Bacterial Regulatory Proteins and an Enzyme Involved in Antibiotic Biosynthesis. [Doctoral Dissertation]. University of Wisconsin – Milwaukee; 2017. Available from: https://dc.uwm.edu/etd/1636


University of Toledo

14. Dajnowicz, Steven. Electronic Modulation in Pyridoxal-5’-Phosphate-Dependent Enzymes.

Degree: PhD, Chemistry, 2018, University of Toledo

 Pyridoxal 5’-phosphate (PLP, vitamin B6) is one of the most ubiquitous cofactors found in biological systems. PLP-dependent enzymes are essential proteins that catalyze a diverse… (more)

Subjects/Keywords: Chemistry; Biochemistry; Physical Chemistry; Vitamin B6; pyridoxal 5 phosphate; aspartate aminotransferase; biocatalysts; quantum chemistry; molecular dynamics; protein dynamics; natural bond orbitals

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APA (6th Edition):

Dajnowicz, S. (2018). Electronic Modulation in Pyridoxal-5’-Phosphate-Dependent Enzymes. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1542039760697676

Chicago Manual of Style (16th Edition):

Dajnowicz, Steven. “Electronic Modulation in Pyridoxal-5’-Phosphate-Dependent Enzymes.” 2018. Doctoral Dissertation, University of Toledo. Accessed July 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1542039760697676.

MLA Handbook (7th Edition):

Dajnowicz, Steven. “Electronic Modulation in Pyridoxal-5’-Phosphate-Dependent Enzymes.” 2018. Web. 22 Jul 2019.

Vancouver:

Dajnowicz S. Electronic Modulation in Pyridoxal-5’-Phosphate-Dependent Enzymes. [Internet] [Doctoral dissertation]. University of Toledo; 2018. [cited 2019 Jul 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1542039760697676.

Council of Science Editors:

Dajnowicz S. Electronic Modulation in Pyridoxal-5’-Phosphate-Dependent Enzymes. [Doctoral Dissertation]. University of Toledo; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1542039760697676

15. Elliott, Sarah. Regulation of the ESX-5 Secretion System in Mycobacterium tuberculosis.

Degree: PhD, Microbiology, Immunology and Cancer Biology, 2017, University of Minnesota

 Mycobacterium tuberculosis (Mtb) is one of the most prolific bacterial pathogens in the history of human disease. Robert Koch discovered that Mtb was the causative… (more)

Subjects/Keywords: ESX-5; Mycobacterium tuberculosis; Phosphate; Secretion

…1 Chapter 2: Phosphate starvation: a novel signal that triggers ESX-5 secretion in… …found that mutating the esx-5 RegX3 binding site sequence reversed expression of esx5… …transcripts and secretion of EsxN and PPE41 in WT Mtb during Pi limitation. Similarly, esx-5… …overexpression and ESX-5 hyper-secretion was suppressed in the ΔpstA1 mutant when the RegX3 binding… …regulation of ESX-5 for Mtb virulence by infecting C57BL/6 and IrgM1-/- mice with a binding site… 

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APA (6th Edition):

Elliott, S. (2017). Regulation of the ESX-5 Secretion System in Mycobacterium tuberculosis. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/188843

Chicago Manual of Style (16th Edition):

Elliott, Sarah. “Regulation of the ESX-5 Secretion System in Mycobacterium tuberculosis.” 2017. Doctoral Dissertation, University of Minnesota. Accessed July 22, 2019. http://hdl.handle.net/11299/188843.

MLA Handbook (7th Edition):

Elliott, Sarah. “Regulation of the ESX-5 Secretion System in Mycobacterium tuberculosis.” 2017. Web. 22 Jul 2019.

Vancouver:

Elliott S. Regulation of the ESX-5 Secretion System in Mycobacterium tuberculosis. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/11299/188843.

Council of Science Editors:

Elliott S. Regulation of the ESX-5 Secretion System in Mycobacterium tuberculosis. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/188843


Virginia Tech

16. Miller, Danielle Virginia. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.

Degree: PhD, Biochemistry, 2017, Virginia Tech

 S-Adenosyl-L-methionine (SAM) is an essential metabolite for all domains of life. SAM- dependent reactions result in three major metabolites: S-adenosyl-L-homocysteine (SAH), methylthioadenosine (MTA), and 5'-deoxyadenosine… (more)

Subjects/Keywords: S-adenosyl-L-methionine; SAM; recycling; 6-deoxy-5-ketofructose 1-phosphate; aromatic amino acids; methionine salvage; 5'-deoxyadenosine; S-adenosylhomoysteine; methylthioadenosine

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APA (6th Edition):

Miller, D. V. (2017). Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77520

Chicago Manual of Style (16th Edition):

Miller, Danielle Virginia. “Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.” 2017. Doctoral Dissertation, Virginia Tech. Accessed July 22, 2019. http://hdl.handle.net/10919/77520.

MLA Handbook (7th Edition):

Miller, Danielle Virginia. “Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.” 2017. Web. 22 Jul 2019.

Vancouver:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10919/77520.

Council of Science Editors:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/77520


University of Bath

17. Sunderland, Peter T. Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2.

Degree: PhD, 2010, University of Bath

Subjects/Keywords: 615; 5-AIQ; poly(ADP-ribose)polymerase; isoform selectivity; DNA repair; isoquinolin-1-ones

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APA (6th Edition):

Sunderland, P. T. (2010). Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2. (Doctoral Dissertation). University of Bath. Retrieved from https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371

Chicago Manual of Style (16th Edition):

Sunderland, Peter T. “Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2.” 2010. Doctoral Dissertation, University of Bath. Accessed July 22, 2019. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371.

MLA Handbook (7th Edition):

Sunderland, Peter T. “Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2.” 2010. Web. 22 Jul 2019.

Vancouver:

Sunderland PT. Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2. [Internet] [Doctoral dissertation]. University of Bath; 2010. [cited 2019 Jul 22]. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371.

Council of Science Editors:

Sunderland PT. Design and synthesis of selective inhibitors of poly(ADP-ribose)polymerase-2. [Doctoral Dissertation]. University of Bath; 2010. Available from: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.528371


University of Cambridge

18. Xia, Yang. The localisation and regulation of phosphatidylinositol-4-phosphate 5-Kinase gamma splice variants and the discovery of a new mammalian splice variant, PIP5KIγ_v6.

Degree: PhD, 2011, University of Cambridge

 Type I PIP kinases (phosphatidylinositol 4-phosphate 5-kinases, PIP5Ks) catalyse the majority of cellular synthesis of PI(4,5)P2. To date, three mammalian isoforms (r1, r2, r3) have… (more)

Subjects/Keywords: 615.1; Phosphatidylinositol 4-phosphate 5-kinase I gamma; Type I PIP5K; Phosphorylation; Alternative splicing; Discovery; Subcellular localisation; Confocal microscopy; Polymerase chain reaction; Kinase assay; Autophosphorylation

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APA (6th Edition):

Xia, Y. (2011). The localisation and regulation of phosphatidylinositol-4-phosphate 5-Kinase gamma splice variants and the discovery of a new mammalian splice variant, PIP5KIγ_v6. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/240633 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555206

Chicago Manual of Style (16th Edition):

Xia, Yang. “The localisation and regulation of phosphatidylinositol-4-phosphate 5-Kinase gamma splice variants and the discovery of a new mammalian splice variant, PIP5KIγ_v6.” 2011. Doctoral Dissertation, University of Cambridge. Accessed July 22, 2019. https://www.repository.cam.ac.uk/handle/1810/240633 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555206.

MLA Handbook (7th Edition):

Xia, Yang. “The localisation and regulation of phosphatidylinositol-4-phosphate 5-Kinase gamma splice variants and the discovery of a new mammalian splice variant, PIP5KIγ_v6.” 2011. Web. 22 Jul 2019.

Vancouver:

Xia Y. The localisation and regulation of phosphatidylinositol-4-phosphate 5-Kinase gamma splice variants and the discovery of a new mammalian splice variant, PIP5KIγ_v6. [Internet] [Doctoral dissertation]. University of Cambridge; 2011. [cited 2019 Jul 22]. Available from: https://www.repository.cam.ac.uk/handle/1810/240633 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555206.

Council of Science Editors:

Xia Y. The localisation and regulation of phosphatidylinositol-4-phosphate 5-Kinase gamma splice variants and the discovery of a new mammalian splice variant, PIP5KIγ_v6. [Doctoral Dissertation]. University of Cambridge; 2011. Available from: https://www.repository.cam.ac.uk/handle/1810/240633 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555206


University of Illinois – Urbana-Champaign

19. Lambrecht, Michael. The chemical and enzymatic synthesis of poly(ADP-ribose).

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Poly(ADP-ribose) synthesis and degradation are important cellular processes associated with the DNA damage response and many other pathways. Traditionally, these processes have been challenging to… (more)

Subjects/Keywords: Poly(ADP-ribose); Total Synthesis; Enzymatic Synthesis; Poly(ADP-ribose) Polymerase; Poly ADP ribose polymerase (PARP); Poly(ADP-ribose) Glycohydrolase (PARG); Raptinal

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APA (6th Edition):

Lambrecht, M. (2016). The chemical and enzymatic synthesis of poly(ADP-ribose). (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/92923

Chicago Manual of Style (16th Edition):

Lambrecht, Michael. “The chemical and enzymatic synthesis of poly(ADP-ribose).” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 22, 2019. http://hdl.handle.net/2142/92923.

MLA Handbook (7th Edition):

Lambrecht, Michael. “The chemical and enzymatic synthesis of poly(ADP-ribose).” 2016. Web. 22 Jul 2019.

Vancouver:

Lambrecht M. The chemical and enzymatic synthesis of poly(ADP-ribose). [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2142/92923.

Council of Science Editors:

Lambrecht M. The chemical and enzymatic synthesis of poly(ADP-ribose). [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/92923


Virginia Tech

20. Edmonds, Yvette M. Toward a Quantitative Analysis of PARP-1 and Poly(ADP-ribosyl)ation in Cellular Senescence.

Degree: PhD, Biochemistry, 2010, Virginia Tech

 Aging is a complicated and multifactorial phenomenon. Model systems involving the induction of replicative senescence in cultured cells have been indispensable in elucidating some of… (more)

Subjects/Keywords: cellular senescence; mass spectrometry; nicotinamide; poly(ADP-ribose); poly(ADP-ribose polymerase); replicative senescence

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APA (6th Edition):

Edmonds, Y. M. (2010). Toward a Quantitative Analysis of PARP-1 and Poly(ADP-ribosyl)ation in Cellular Senescence. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/39180

Chicago Manual of Style (16th Edition):

Edmonds, Yvette M. “Toward a Quantitative Analysis of PARP-1 and Poly(ADP-ribosyl)ation in Cellular Senescence.” 2010. Doctoral Dissertation, Virginia Tech. Accessed July 22, 2019. http://hdl.handle.net/10919/39180.

MLA Handbook (7th Edition):

Edmonds, Yvette M. “Toward a Quantitative Analysis of PARP-1 and Poly(ADP-ribosyl)ation in Cellular Senescence.” 2010. Web. 22 Jul 2019.

Vancouver:

Edmonds YM. Toward a Quantitative Analysis of PARP-1 and Poly(ADP-ribosyl)ation in Cellular Senescence. [Internet] [Doctoral dissertation]. Virginia Tech; 2010. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/10919/39180.

Council of Science Editors:

Edmonds YM. Toward a Quantitative Analysis of PARP-1 and Poly(ADP-ribosyl)ation in Cellular Senescence. [Doctoral Dissertation]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/39180


University of Notre Dame

21. Julia T Philip. Development of a yeast-based sensor for environmental monitoring</h1>.

Degree: PhD, Chemistry and Biochemistry, 2013, University of Notre Dame

  Part 1: MTBindingSim MTBindingSim is a program that simulates binding curves for proteins binding to microtubules. The operation of the program, the experimental methods… (more)

Subjects/Keywords: phosphate; biosensor

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APA (6th Edition):

Philip, J. T. (2013). Development of a yeast-based sensor for environmental monitoring</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/ww72b853q8c

Chicago Manual of Style (16th Edition):

Philip, Julia T. “Development of a yeast-based sensor for environmental monitoring</h1>.” 2013. Doctoral Dissertation, University of Notre Dame. Accessed July 22, 2019. https://curate.nd.edu/show/ww72b853q8c.

MLA Handbook (7th Edition):

Philip, Julia T. “Development of a yeast-based sensor for environmental monitoring</h1>.” 2013. Web. 22 Jul 2019.

Vancouver:

Philip JT. Development of a yeast-based sensor for environmental monitoring</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2013. [cited 2019 Jul 22]. Available from: https://curate.nd.edu/show/ww72b853q8c.

Council of Science Editors:

Philip JT. Development of a yeast-based sensor for environmental monitoring</h1>. [Doctoral Dissertation]. University of Notre Dame; 2013. Available from: https://curate.nd.edu/show/ww72b853q8c


University of Western Australia

22. Cluning, Carmel. Steroid receptor-associated immunophilins : influence of targeted knockdown and altered expression on receptor signalling.

Degree: PhD, 2007, University of Western Australia

 [Truncated abstract] Steroid receptors belong to the superfamily of nuclear receptors, and include the androgen receptor (AR), estrogen receptors (ER[alpha] and ER[beta], glucocorticoid receptor (GR),… (more)

Subjects/Keywords: Hormones, Sex; Peptidylprolyl isomerase; Immunophilins; Steroid receptors

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APA (6th Edition):

Cluning, C. (2007). Steroid receptor-associated immunophilins : influence of targeted knockdown and altered expression on receptor signalling. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=10518&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Cluning, Carmel. “Steroid receptor-associated immunophilins : influence of targeted knockdown and altered expression on receptor signalling.” 2007. Doctoral Dissertation, University of Western Australia. Accessed July 22, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=10518&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Cluning, Carmel. “Steroid receptor-associated immunophilins : influence of targeted knockdown and altered expression on receptor signalling.” 2007. Web. 22 Jul 2019.

Vancouver:

Cluning C. Steroid receptor-associated immunophilins : influence of targeted knockdown and altered expression on receptor signalling. [Internet] [Doctoral dissertation]. University of Western Australia; 2007. [cited 2019 Jul 22]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=10518&local_base=GEN01-INS01.

Council of Science Editors:

Cluning C. Steroid receptor-associated immunophilins : influence of targeted knockdown and altered expression on receptor signalling. [Doctoral Dissertation]. University of Western Australia; 2007. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=10518&local_base=GEN01-INS01


Case Western Reserve University

23. Kiser, Philip David. STRUCTURAL AND BIOCHEMICAL STUDIES OF RPE65, THE RETINOID ISOMERASE OF THE VISUAL CYCLE.

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

 Vertebrate vision is maintained by the retinoid (visual) cycle, a complex enzymatic pathway that operates in the retina to regenerate the visual chromophore, 11-cis-retinal. A… (more)

Subjects/Keywords: Biochemistry; Retinoids; monotopic membrane protein; isomerase; metalloprotein

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APA (6th Edition):

Kiser, P. D. (2010). STRUCTURAL AND BIOCHEMICAL STUDIES OF RPE65, THE RETINOID ISOMERASE OF THE VISUAL CYCLE. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1269869379

Chicago Manual of Style (16th Edition):

Kiser, Philip David. “STRUCTURAL AND BIOCHEMICAL STUDIES OF RPE65, THE RETINOID ISOMERASE OF THE VISUAL CYCLE.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed July 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1269869379.

MLA Handbook (7th Edition):

Kiser, Philip David. “STRUCTURAL AND BIOCHEMICAL STUDIES OF RPE65, THE RETINOID ISOMERASE OF THE VISUAL CYCLE.” 2010. Web. 22 Jul 2019.

Vancouver:

Kiser PD. STRUCTURAL AND BIOCHEMICAL STUDIES OF RPE65, THE RETINOID ISOMERASE OF THE VISUAL CYCLE. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2019 Jul 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1269869379.

Council of Science Editors:

Kiser PD. STRUCTURAL AND BIOCHEMICAL STUDIES OF RPE65, THE RETINOID ISOMERASE OF THE VISUAL CYCLE. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1269869379

24. Marylane de Sousa. ObtenÃÃo de um catalisador insolÃvel para a produÃÃo de D-tagatose por L-arabinose isomerase.

Degree: PhD, 2015, Universidade Federal do Ceará

Dentro das possibilidades terapÃuticas atuais para o tratamento de pacientes com problemas congÃnitos de metabolismo, a dieta constitui o pilar mais importante e a D-tagatose… (more)

Subjects/Keywords: ENGENHARIAS; Engenharia quÃmica; L-arabinose isomerase; D-galactose; ImobilizaÃÃo; L-arabinose isomerase; D-galactose; Immobilization

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APA (6th Edition):

Sousa, M. d. (2015). ObtenÃÃo de um catalisador insolÃvel para a produÃÃo de D-tagatose por L-arabinose isomerase. (Doctoral Dissertation). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14779 ;

Chicago Manual of Style (16th Edition):

Sousa, Marylane de. “ObtenÃÃo de um catalisador insolÃvel para a produÃÃo de D-tagatose por L-arabinose isomerase.” 2015. Doctoral Dissertation, Universidade Federal do Ceará. Accessed July 22, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14779 ;.

MLA Handbook (7th Edition):

Sousa, Marylane de. “ObtenÃÃo de um catalisador insolÃvel para a produÃÃo de D-tagatose por L-arabinose isomerase.” 2015. Web. 22 Jul 2019.

Vancouver:

Sousa Md. ObtenÃÃo de um catalisador insolÃvel para a produÃÃo de D-tagatose por L-arabinose isomerase. [Internet] [Doctoral dissertation]. Universidade Federal do Ceará 2015. [cited 2019 Jul 22]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14779 ;.

Council of Science Editors:

Sousa Md. ObtenÃÃo de um catalisador insolÃvel para a produÃÃo de D-tagatose por L-arabinose isomerase. [Doctoral Dissertation]. Universidade Federal do Ceará 2015. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=14779 ;

25. Glenn, Katie. Allosteric Regulation of Bacterial and Fungal Xylulose 5-phosphate/ Fructose 6-phosphate Phosphoketolases (Xfps).

Degree: PhD, Biochemistry and Molecular Biology, 2014, Clemson University

  Acetate is excreted as a metabolic end product in many microbes. Acetate production has primarily been studied in bacteria and archaea but is known… (more)

Subjects/Keywords: Acetate; Allosteric Enzyme; Allosteric Regulation; Cryptococcus neoformans; Xfp; Xylulose 5-phosphate/ Fructose 6-phosphate Phosphoketolase; Biochemistry; Molecular Biology

…reaction to convert X5P or ribose 5-phosphate to G3P or sedoheptulose 7-phosphate respectively… …3 Xylulose 5-phosphate/Fructose 6-phosphate Phosphoketolase (Xfp) .... 12… …23 II. BIOCHEMICAL AND KINETICH CHARACTERIZATION OF XYLULOSE 5-PHOSPHATE FRUCTOSE 6… …58 III. ALLOSTERIC REGULATION OF LACTOBACILLUS PLANTARUM XYLULOSE 5-PHOSPHATE/ FRUCTOSE 6… …143 xii CHAPTER 1 LITERATURE REVIEW OF XYLULOSE 5-PHOSPHATE/ FRUCTOSE 6PHOSPHATE… 

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APA (6th Edition):

Glenn, K. (2014). Allosteric Regulation of Bacterial and Fungal Xylulose 5-phosphate/ Fructose 6-phosphate Phosphoketolases (Xfps). (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1454

Chicago Manual of Style (16th Edition):

Glenn, Katie. “Allosteric Regulation of Bacterial and Fungal Xylulose 5-phosphate/ Fructose 6-phosphate Phosphoketolases (Xfps).” 2014. Doctoral Dissertation, Clemson University. Accessed July 22, 2019. https://tigerprints.clemson.edu/all_dissertations/1454.

MLA Handbook (7th Edition):

Glenn, Katie. “Allosteric Regulation of Bacterial and Fungal Xylulose 5-phosphate/ Fructose 6-phosphate Phosphoketolases (Xfps).” 2014. Web. 22 Jul 2019.

Vancouver:

Glenn K. Allosteric Regulation of Bacterial and Fungal Xylulose 5-phosphate/ Fructose 6-phosphate Phosphoketolases (Xfps). [Internet] [Doctoral dissertation]. Clemson University; 2014. [cited 2019 Jul 22]. Available from: https://tigerprints.clemson.edu/all_dissertations/1454.

Council of Science Editors:

Glenn K. Allosteric Regulation of Bacterial and Fungal Xylulose 5-phosphate/ Fructose 6-phosphate Phosphoketolases (Xfps). [Doctoral Dissertation]. Clemson University; 2014. Available from: https://tigerprints.clemson.edu/all_dissertations/1454


Utah State University

26. Farr, Craig H. Influence of 2,5-Hexanedione, Acrylamide, tri-o-totyl Phoshate, Leptophos and Methylmercury on Endogenous Levels of Tryptophan, Serotonin and 5-Hydroxyindoleacetic Acid and Serotonin Turnover Rates in Rat Brain.

Degree: PhD, Animal, Dairy, and Veterinary Sciences, 1992, Utah State University

  Several industrial and environmental chemicals cause distal and/or central neuropathy among other diverse toxic effects. Spague-Dawley derived rats were fed doses of 2,5-hexanedione, acrylamide,… (more)

Subjects/Keywords: influence; 2; 5-hexanedione; acrylamide; tri-o-totyl; phosphate; leptohpos; methylmercury; endogenous; levels; tryptophan; serotonin; acid; turnover; rates; rat; brain; Toxicology

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APA (6th Edition):

Farr, C. H. (1992). Influence of 2,5-Hexanedione, Acrylamide, tri-o-totyl Phoshate, Leptophos and Methylmercury on Endogenous Levels of Tryptophan, Serotonin and 5-Hydroxyindoleacetic Acid and Serotonin Turnover Rates in Rat Brain. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/4198

Chicago Manual of Style (16th Edition):

Farr, Craig H. “Influence of 2,5-Hexanedione, Acrylamide, tri-o-totyl Phoshate, Leptophos and Methylmercury on Endogenous Levels of Tryptophan, Serotonin and 5-Hydroxyindoleacetic Acid and Serotonin Turnover Rates in Rat Brain.” 1992. Doctoral Dissertation, Utah State University. Accessed July 22, 2019. https://digitalcommons.usu.edu/etd/4198.

MLA Handbook (7th Edition):

Farr, Craig H. “Influence of 2,5-Hexanedione, Acrylamide, tri-o-totyl Phoshate, Leptophos and Methylmercury on Endogenous Levels of Tryptophan, Serotonin and 5-Hydroxyindoleacetic Acid and Serotonin Turnover Rates in Rat Brain.” 1992. Web. 22 Jul 2019.

Vancouver:

Farr CH. Influence of 2,5-Hexanedione, Acrylamide, tri-o-totyl Phoshate, Leptophos and Methylmercury on Endogenous Levels of Tryptophan, Serotonin and 5-Hydroxyindoleacetic Acid and Serotonin Turnover Rates in Rat Brain. [Internet] [Doctoral dissertation]. Utah State University; 1992. [cited 2019 Jul 22]. Available from: https://digitalcommons.usu.edu/etd/4198.

Council of Science Editors:

Farr CH. Influence of 2,5-Hexanedione, Acrylamide, tri-o-totyl Phoshate, Leptophos and Methylmercury on Endogenous Levels of Tryptophan, Serotonin and 5-Hydroxyindoleacetic Acid and Serotonin Turnover Rates in Rat Brain. [Doctoral Dissertation]. Utah State University; 1992. Available from: https://digitalcommons.usu.edu/etd/4198


Virginia Commonwealth University

27. Gandhi, Amit. VITAMIN B6 METABOLISM AND REGULATION OF PYRIDOXAL KINASE.

Degree: PhD, Medicinal Chemistry, 2009, Virginia Commonwealth University

 Pyridoxal 5'-phosphate (PLP) is the cofactor for over 140 vitamin B6 (PLP)-dependent enzymes that are involved in various metabolic and biosynthetic pathways. Pyridoxal kinase (PL… (more)

Subjects/Keywords: Vitamin B6; Pyridoxal Kinase; Pyridoxal 5'-phosphate; Chemicals and Drugs; Medicine and Health Sciences

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APA (6th Edition):

Gandhi, A. (2009). VITAMIN B6 METABOLISM AND REGULATION OF PYRIDOXAL KINASE. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2008

Chicago Manual of Style (16th Edition):

Gandhi, Amit. “VITAMIN B6 METABOLISM AND REGULATION OF PYRIDOXAL KINASE.” 2009. Doctoral Dissertation, Virginia Commonwealth University. Accessed July 22, 2019. https://scholarscompass.vcu.edu/etd/2008.

MLA Handbook (7th Edition):

Gandhi, Amit. “VITAMIN B6 METABOLISM AND REGULATION OF PYRIDOXAL KINASE.” 2009. Web. 22 Jul 2019.

Vancouver:

Gandhi A. VITAMIN B6 METABOLISM AND REGULATION OF PYRIDOXAL KINASE. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2009. [cited 2019 Jul 22]. Available from: https://scholarscompass.vcu.edu/etd/2008.

Council of Science Editors:

Gandhi A. VITAMIN B6 METABOLISM AND REGULATION OF PYRIDOXAL KINASE. [Doctoral Dissertation]. Virginia Commonwealth University; 2009. Available from: https://scholarscompass.vcu.edu/etd/2008


University of Aberdeen

28. Thammakan, Nirawan. Synthesis and characterisation of calcium phosphate compositions by precipitation and 'biomimetic methods'.

Degree: PhD, 2016, University of Aberdeen

 Calcium phosphate compounds have been widely utilised in the interdisciplinary field of biomaterials research and are used clinically in a number of medical devices. In… (more)

Subjects/Keywords: 610.28; Calcium phosphate

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APA (6th Edition):

Thammakan, N. (2016). Synthesis and characterisation of calcium phosphate compositions by precipitation and 'biomimetic methods'. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=230656 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.694692

Chicago Manual of Style (16th Edition):

Thammakan, Nirawan. “Synthesis and characterisation of calcium phosphate compositions by precipitation and 'biomimetic methods'.” 2016. Doctoral Dissertation, University of Aberdeen. Accessed July 22, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=230656 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.694692.

MLA Handbook (7th Edition):

Thammakan, Nirawan. “Synthesis and characterisation of calcium phosphate compositions by precipitation and 'biomimetic methods'.” 2016. Web. 22 Jul 2019.

Vancouver:

Thammakan N. Synthesis and characterisation of calcium phosphate compositions by precipitation and 'biomimetic methods'. [Internet] [Doctoral dissertation]. University of Aberdeen; 2016. [cited 2019 Jul 22]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=230656 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.694692.

Council of Science Editors:

Thammakan N. Synthesis and characterisation of calcium phosphate compositions by precipitation and 'biomimetic methods'. [Doctoral Dissertation]. University of Aberdeen; 2016. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=230656 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.694692


Oregon State University

29. Park, Deok-Hie. Aqueous Niobium Chemistry at Low pH: New Precursors for Oxide Thin Films.

Degree: PhD, 2017, Oregon State University

Phosphate and peroxide stabilize new oxo-hydroxo niobium clusters in water at low pH. The clusters open a new chapter in aqueous niobium chemistry under acidic… (more)

Subjects/Keywords: Niobium oxide phosphate

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APA (6th Edition):

Park, D. (2017). Aqueous Niobium Chemistry at Low pH: New Precursors for Oxide Thin Films. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/61704

Chicago Manual of Style (16th Edition):

Park, Deok-Hie. “Aqueous Niobium Chemistry at Low pH: New Precursors for Oxide Thin Films.” 2017. Doctoral Dissertation, Oregon State University. Accessed July 22, 2019. http://hdl.handle.net/1957/61704.

MLA Handbook (7th Edition):

Park, Deok-Hie. “Aqueous Niobium Chemistry at Low pH: New Precursors for Oxide Thin Films.” 2017. Web. 22 Jul 2019.

Vancouver:

Park D. Aqueous Niobium Chemistry at Low pH: New Precursors for Oxide Thin Films. [Internet] [Doctoral dissertation]. Oregon State University; 2017. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/1957/61704.

Council of Science Editors:

Park D. Aqueous Niobium Chemistry at Low pH: New Precursors for Oxide Thin Films. [Doctoral Dissertation]. Oregon State University; 2017. Available from: http://hdl.handle.net/1957/61704

30. Cracan, Valentin F. Structure, Function and Metabolic Roles of IcmF-a Fusion Between the Radical B12 Enzyme and its G-protein Chaperone.

Degree: PhD, Biological Chemistry, 2012, University of Michigan

 Coenzyme B12 is a biologically active form of vitamin B12 and used in Nature as a radical reservoir to catalyze chemically challenging transformations. The loading… (more)

Subjects/Keywords: IcmF Is a Fusion Between a Coenzyme B12-dependent Isobutyryl-CoA/N-butyryl-CoA Isomerase and a G-protein Chaperone.; AdoCbl, 5'-Deoxy-5'-Adenosylcobalamin; IcmF Also Isomerizes Isovaleryl-CoA to Pivalyl-CoA.; Biological Chemistry; Science

…94 3.4.5 Loss of 5´-deoxyadenosine leads to inactivation of IcmF… …141 CHAPTER 5: Ongoing Work and Future Directions… …and 5'-deoxyadenosine during enzyme-monitored turnover… …92 Table 3.2 Kinetics of OH2Cbl and 5´-deoxyadenosine formation… …160 xv LIST OF ABBREVIATIONS AdoCbi, 5'-deoxy-5'-adenosylcobinamide; AdoCbl, 5… 

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

APA (6th Edition):

Cracan, V. F. (2012). Structure, Function and Metabolic Roles of IcmF-a Fusion Between the Radical B12 Enzyme and its G-protein Chaperone. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/91597

Chicago Manual of Style (16th Edition):

Cracan, Valentin F. “Structure, Function and Metabolic Roles of IcmF-a Fusion Between the Radical B12 Enzyme and its G-protein Chaperone.” 2012. Doctoral Dissertation, University of Michigan. Accessed July 22, 2019. http://hdl.handle.net/2027.42/91597.

MLA Handbook (7th Edition):

Cracan, Valentin F. “Structure, Function and Metabolic Roles of IcmF-a Fusion Between the Radical B12 Enzyme and its G-protein Chaperone.” 2012. Web. 22 Jul 2019.

Vancouver:

Cracan VF. Structure, Function and Metabolic Roles of IcmF-a Fusion Between the Radical B12 Enzyme and its G-protein Chaperone. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Jul 22]. Available from: http://hdl.handle.net/2027.42/91597.

Council of Science Editors:

Cracan VF. Structure, Function and Metabolic Roles of IcmF-a Fusion Between the Radical B12 Enzyme and its G-protein Chaperone. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/91597

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