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You searched for subject:(ribose 5 phosphate isomerase). Showing records 1 – 30 of 1708 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 17, 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. 17 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 17]. 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


Vrije Universiteit Amsterdam

2. Wamelink, M.M.C. Pentose phosphate pathway : biochemistry, metabolism and inherited defects .

Degree: 2008, Vrije Universiteit Amsterdam

Subjects/Keywords: Pentose fosfaat route: biochemie, metabolisme en erfelijke ziekten; pentose phosphate pathway; transaldolase deficiency; ribose-5-phosphate isomerase deficiency; sedoheptulose; sedoheptulokinase; polyols; sugarphosphates

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APA (6th Edition):

Wamelink, M. M. C. (2008). Pentose phosphate pathway : biochemistry, metabolism and inherited defects . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/13054

Chicago Manual of Style (16th Edition):

Wamelink, M M C. “Pentose phosphate pathway : biochemistry, metabolism and inherited defects .” 2008. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed July 17, 2019. http://hdl.handle.net/1871/13054.

MLA Handbook (7th Edition):

Wamelink, M M C. “Pentose phosphate pathway : biochemistry, metabolism and inherited defects .” 2008. Web. 17 Jul 2019.

Vancouver:

Wamelink MMC. Pentose phosphate pathway : biochemistry, metabolism and inherited defects . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2008. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1871/13054.

Council of Science Editors:

Wamelink MMC. Pentose phosphate pathway : biochemistry, metabolism and inherited defects . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2008. Available from: http://hdl.handle.net/1871/13054


University of Georgia

3. 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 17, 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. 17 Jul 2019.

Vancouver:

Lima S. Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes. [Internet] [Doctoral dissertation]. University of Georgia; 2008. [cited 2019 Jul 17]. 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

4. 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 17, 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. 17 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 17]. 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

5. 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 17, 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. 17 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 17]. 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

6. Paracuellos torrecilla, Patricia. Étude structurale et fonctionnelle d’une sérine/thréonine kinase de staphylococcus aureus : Structural and functional analysis of a serine/threonine kinase from staphylococcus aureus.

Degree: Docteur es, Biochimie, 2009, Université Claude Bernard – Lyon I

Les réactions de phosphorylation / déphosphorylation chez les bactéries régulent plusieurs fonctions cellulaires telles que croissance, différenciation, pathogénie, résistance aux antibiotiques, réponse au stress, formation… (more)

Subjects/Keywords: Triose phosphate isomérase; Staphylococcus aureus; Domaine PASTA; Sérine/thréonine kinase Stk1; Phosphorylation; PASTA domains; Triose phosphate isomerase; Phosphorylation

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APA (6th Edition):

Paracuellos torrecilla, P. (2009). Étude structurale et fonctionnelle d’une sérine/thréonine kinase de staphylococcus aureus : Structural and functional analysis of a serine/threonine kinase from staphylococcus aureus. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2009LYO10211

Chicago Manual of Style (16th Edition):

Paracuellos torrecilla, Patricia. “Étude structurale et fonctionnelle d’une sérine/thréonine kinase de staphylococcus aureus : Structural and functional analysis of a serine/threonine kinase from staphylococcus aureus.” 2009. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed July 17, 2019. http://www.theses.fr/2009LYO10211.

MLA Handbook (7th Edition):

Paracuellos torrecilla, Patricia. “Étude structurale et fonctionnelle d’une sérine/thréonine kinase de staphylococcus aureus : Structural and functional analysis of a serine/threonine kinase from staphylococcus aureus.” 2009. Web. 17 Jul 2019.

Vancouver:

Paracuellos torrecilla P. Étude structurale et fonctionnelle d’une sérine/thréonine kinase de staphylococcus aureus : Structural and functional analysis of a serine/threonine kinase from staphylococcus aureus. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2009. [cited 2019 Jul 17]. Available from: http://www.theses.fr/2009LYO10211.

Council of Science Editors:

Paracuellos torrecilla P. Étude structurale et fonctionnelle d’une sérine/thréonine kinase de staphylococcus aureus : Structural and functional analysis of a serine/threonine kinase from staphylococcus aureus. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2009. Available from: http://www.theses.fr/2009LYO10211

7. 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 17, 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. 17 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 17]. 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

8. 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 17, 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. 17 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 17]. 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

9. 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 17, 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. 17 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 17]. 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

10. 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 17, 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. 17 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 17]. 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

11. 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 17, 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. 17 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 17]. 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

12. Montel, Sonia. La 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, une métalloenzyme cible pour l'élaboration d'inhibiteurs chélatants : The 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, a target metalloenzyme for the elaboration of chelation-based inhibitors.

Degree: Docteur es, Ingénierie biomoléculaire, 2012, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier)

La voie non-mévalonate est fortement présente chez les plantes et les bactéries mais est absente chez les mammifères. C'est pourquoi inhiber la synthèse des isoprénoïdes… (more)

Subjects/Keywords: 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase; Métalloenzyme; Inhibiteurs; Chélatants; Phytosanitaire; 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase; Metalloenzyme; Inhibitors; Chelation; Agrochemical

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APA (6th Edition):

Montel, S. (2012). La 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, une métalloenzyme cible pour l'élaboration d'inhibiteurs chélatants : The 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, a target metalloenzyme for the elaboration of chelation-based inhibitors. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Retrieved from http://www.theses.fr/2012ENCM0013

Chicago Manual of Style (16th Edition):

Montel, Sonia. “La 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, une métalloenzyme cible pour l'élaboration d'inhibiteurs chélatants : The 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, a target metalloenzyme for the elaboration of chelation-based inhibitors.” 2012. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Accessed July 17, 2019. http://www.theses.fr/2012ENCM0013.

MLA Handbook (7th Edition):

Montel, Sonia. “La 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, une métalloenzyme cible pour l'élaboration d'inhibiteurs chélatants : The 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, a target metalloenzyme for the elaboration of chelation-based inhibitors.” 2012. Web. 17 Jul 2019.

Vancouver:

Montel S. La 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, une métalloenzyme cible pour l'élaboration d'inhibiteurs chélatants : The 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, a target metalloenzyme for the elaboration of chelation-based inhibitors. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2012. [cited 2019 Jul 17]. Available from: http://www.theses.fr/2012ENCM0013.

Council of Science Editors:

Montel S. La 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, une métalloenzyme cible pour l'élaboration d'inhibiteurs chélatants : The 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase, a target metalloenzyme for the elaboration of chelation-based inhibitors. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2012. Available from: http://www.theses.fr/2012ENCM0013


University of Alberta

13. 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 17, 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. 17 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 17]. 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

14. 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 17, 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. 17 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 17]. 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


University of Manchester

15. Grainger, Deborah. Investigation of Phosphatidylinositol 5-Phosphate’s Role in Insulin-Stimulated Glucose Uptake in a Skeletal Muscle Cell Line.

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

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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 http://www.manchester.ac.uk/escholar/uk-ac-man-scw:102788

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 17, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:102788.

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. 17 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 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:102788.

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: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:102788


Virginia Tech

16. 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 17, 2019. http://hdl.handle.net/10919/50528.

MLA Handbook (7th Edition):

Liu, Pingyang. “Biochemical studies of enzymes in insect cuticle hardening.” 2013. Web. 17 Jul 2019.

Vancouver:

Liu P. Biochemical studies of enzymes in insect cuticle hardening. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Jul 17]. 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

17. 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 17, 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. 17 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 17]. 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 Kentucky

18. Chawsheen, Hedy. ROLE OF SULFIREDOXIN INTERACTING PROTEINS IN LUNG CANCER DEVELOPMENT.

Degree: 2016, University of Kentucky

 Sulfiredoxin (Srx) is an antioxidant enzyme that can be induced by oxidative stress. It promotes oncogenic phenotypes of cell proliferation, colony formation, migration, and metastasis… (more)

Subjects/Keywords: Sulfiredoxin; thioredoxin domain containing protein 5; protein disulfide isomerase A isoform 6; interaction; function; Medical Cell Biology; Medical Molecular Biology; Medical Toxicology

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APA (6th Edition):

Chawsheen, H. (2016). ROLE OF SULFIREDOXIN INTERACTING PROTEINS IN LUNG CANCER DEVELOPMENT. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/toxicology_etds/13

Chicago Manual of Style (16th Edition):

Chawsheen, Hedy. “ROLE OF SULFIREDOXIN INTERACTING PROTEINS IN LUNG CANCER DEVELOPMENT.” 2016. Doctoral Dissertation, University of Kentucky. Accessed July 17, 2019. https://uknowledge.uky.edu/toxicology_etds/13.

MLA Handbook (7th Edition):

Chawsheen, Hedy. “ROLE OF SULFIREDOXIN INTERACTING PROTEINS IN LUNG CANCER DEVELOPMENT.” 2016. Web. 17 Jul 2019.

Vancouver:

Chawsheen H. ROLE OF SULFIREDOXIN INTERACTING PROTEINS IN LUNG CANCER DEVELOPMENT. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2019 Jul 17]. Available from: https://uknowledge.uky.edu/toxicology_etds/13.

Council of Science Editors:

Chawsheen H. ROLE OF SULFIREDOXIN INTERACTING PROTEINS IN LUNG CANCER DEVELOPMENT. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/toxicology_etds/13


University of Toledo

19. 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 17, 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. 17 Jul 2019.

Vancouver:

Dajnowicz S. Electronic Modulation in Pyridoxal-5’-Phosphate-Dependent Enzymes. [Internet] [Doctoral dissertation]. University of Toledo; 2018. [cited 2019 Jul 17]. 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

20. 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 17, 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. 17 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 17]. 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

21. 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 17, 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. 17 Jul 2019.

Vancouver:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Jul 17]. 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


Delft University of Technology

22. Kuijper, S.M. Engineering of Saccharomyces cerevisiae for the production of fuel ethanol from xylose.

Degree: 2006, Delft University of Technology

 For various reasons mankind is looking for alternatives for fossil fuels. One of these alternatives is ethanol made from plant biomass. However, the plant material… (more)

Subjects/Keywords: xylose isomerase; piromyces; fermentation; pentose; yeast; bioethanol; lignocellulose; metabolic engineering; evolutionary engineering; pentose phosphate pathway; hemicellulose

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APA (6th Edition):

Kuijper, S. M. (2006). Engineering of Saccharomyces cerevisiae for the production of fuel ethanol from xylose. (Doctoral Dissertation). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586

Chicago Manual of Style (16th Edition):

Kuijper, S M. “Engineering of Saccharomyces cerevisiae for the production of fuel ethanol from xylose.” 2006. Doctoral Dissertation, Delft University of Technology. Accessed July 17, 2019. http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586.

MLA Handbook (7th Edition):

Kuijper, S M. “Engineering of Saccharomyces cerevisiae for the production of fuel ethanol from xylose.” 2006. Web. 17 Jul 2019.

Vancouver:

Kuijper SM. Engineering of Saccharomyces cerevisiae for the production of fuel ethanol from xylose. [Internet] [Doctoral dissertation]. Delft University of Technology; 2006. [cited 2019 Jul 17]. Available from: http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586.

Council of Science Editors:

Kuijper SM. Engineering of Saccharomyces cerevisiae for the production of fuel ethanol from xylose. [Doctoral Dissertation]. Delft University of Technology; 2006. Available from: http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; urn:NBN:nl:ui:24-uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586 ; http://resolver.tudelft.nl/uuid:6c9304a5-9472-4c9b-b8f9-ac966dad3586


University of Arizona

23. Botta, Davide. Strategies for structural studies of poly(ADP-ribose) glycohydrolase: Towards the validation of a novel therapeutic target .

Degree: 2010, University of Arizona

 Poly(ADP-ribosyl)ation is a reversible post-translational modification of histones and nuclear proteins rapidly stimulated by DNA damage. Its homeostasis is a dynamic process regulated by the… (more)

Subjects/Keywords: nicotinamide adenine dinucleotide; poly(ADP-ribose); poly(ADP-ribose) glycohydrolase; poly(ADP-ribose) polymerase

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APA (6th Edition):

Botta, D. (2010). Strategies for structural studies of poly(ADP-ribose) glycohydrolase: Towards the validation of a novel therapeutic target . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/145718

Chicago Manual of Style (16th Edition):

Botta, Davide. “Strategies for structural studies of poly(ADP-ribose) glycohydrolase: Towards the validation of a novel therapeutic target .” 2010. Doctoral Dissertation, University of Arizona. Accessed July 17, 2019. http://hdl.handle.net/10150/145718.

MLA Handbook (7th Edition):

Botta, Davide. “Strategies for structural studies of poly(ADP-ribose) glycohydrolase: Towards the validation of a novel therapeutic target .” 2010. Web. 17 Jul 2019.

Vancouver:

Botta D. Strategies for structural studies of poly(ADP-ribose) glycohydrolase: Towards the validation of a novel therapeutic target . [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10150/145718.

Council of Science Editors:

Botta D. Strategies for structural studies of poly(ADP-ribose) glycohydrolase: Towards the validation of a novel therapeutic target . [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/145718

24. Midrier, Camille. Synthèse de nouveaux analogues de la Fosmidomycine : inhibiteurs potentiels de l'enzyme 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) : Targeting of the 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) enzyme : design and synthesis of new Fosmidomycin analogues as potential herbicides.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2010, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier)

La synthèse enzymatique de terpénoides chez les mammifères provient de la voie mevalonique. Récemment une voie différente a été découverte et s'est révélée être prépondérante… (more)

Subjects/Keywords: Herbicide; Fosmidomycine; 1-Déoxy-D-Xylulose-5-Phosphate Réductoisomerase; Organophosphorés; Addition radicalaire; Couplage par les métaux de transition; Herbicide; Fosmidomycin; 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR); Organophosphorus compounds; Radical Chemistry; Transition metal coupling

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APA (6th Edition):

Midrier, C. (2010). Synthèse de nouveaux analogues de la Fosmidomycine : inhibiteurs potentiels de l'enzyme 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) : Targeting of the 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) enzyme : design and synthesis of new Fosmidomycin analogues as potential herbicides. (Doctoral Dissertation). Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Retrieved from http://www.theses.fr/2010ENCM0009

Chicago Manual of Style (16th Edition):

Midrier, Camille. “Synthèse de nouveaux analogues de la Fosmidomycine : inhibiteurs potentiels de l'enzyme 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) : Targeting of the 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) enzyme : design and synthesis of new Fosmidomycin analogues as potential herbicides.” 2010. Doctoral Dissertation, Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier). Accessed July 17, 2019. http://www.theses.fr/2010ENCM0009.

MLA Handbook (7th Edition):

Midrier, Camille. “Synthèse de nouveaux analogues de la Fosmidomycine : inhibiteurs potentiels de l'enzyme 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) : Targeting of the 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) enzyme : design and synthesis of new Fosmidomycin analogues as potential herbicides.” 2010. Web. 17 Jul 2019.

Vancouver:

Midrier C. Synthèse de nouveaux analogues de la Fosmidomycine : inhibiteurs potentiels de l'enzyme 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) : Targeting of the 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) enzyme : design and synthesis of new Fosmidomycin analogues as potential herbicides. [Internet] [Doctoral dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2010. [cited 2019 Jul 17]. Available from: http://www.theses.fr/2010ENCM0009.

Council of Science Editors:

Midrier C. Synthèse de nouveaux analogues de la Fosmidomycine : inhibiteurs potentiels de l'enzyme 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) : Targeting of the 1-Deoxy-D-Xylulose-5-Phosphate Reductoisomerase (DXR) enzyme : design and synthesis of new Fosmidomycin analogues as potential herbicides. [Doctoral Dissertation]. Montpellier, Ecole nationale supérieure de chimie; Ecole nationale supérieure de chimie (Montpellier); 2010. Available from: http://www.theses.fr/2010ENCM0009


University of Bath

25. 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 17, 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. 17 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 17]. 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

26. Kluskens, L.D. Molecular studies on protein- and carbohydrate-converting ezymes from thermophilic bacteria.

Degree: 2004, NARCIS

Subjects/Keywords: thermofiele bacteriën; enzymactiviteit; eiwitmetabolisme; koolhydraatmetabolisme; pectaat lyase; glucose-6-fosfaat isomerase; Eiwitten en enzymen; thermophilic bacteria; enzyme activity; protein metabolism; carbohydrate metabolism; pectate lyase; glucose-6-phosphate isomerase; Proteins and Enzymes

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APA (6th Edition):

Kluskens, L. D. (2004). Molecular studies on protein- and carbohydrate-converting ezymes from thermophilic bacteria. (Doctoral Dissertation). NARCIS. Retrieved from http://library.wur.nl/WebQuery/wurpubs/325312 ; urn:nbn:nl:ui:32-325312 ; urn:nbn:nl:ui:32-325312 ; http://library.wur.nl/WebQuery/wurpubs/325312

Chicago Manual of Style (16th Edition):

Kluskens, L D. “Molecular studies on protein- and carbohydrate-converting ezymes from thermophilic bacteria.” 2004. Doctoral Dissertation, NARCIS. Accessed July 17, 2019. http://library.wur.nl/WebQuery/wurpubs/325312 ; urn:nbn:nl:ui:32-325312 ; urn:nbn:nl:ui:32-325312 ; http://library.wur.nl/WebQuery/wurpubs/325312.

MLA Handbook (7th Edition):

Kluskens, L D. “Molecular studies on protein- and carbohydrate-converting ezymes from thermophilic bacteria.” 2004. Web. 17 Jul 2019.

Vancouver:

Kluskens LD. Molecular studies on protein- and carbohydrate-converting ezymes from thermophilic bacteria. [Internet] [Doctoral dissertation]. NARCIS; 2004. [cited 2019 Jul 17]. Available from: http://library.wur.nl/WebQuery/wurpubs/325312 ; urn:nbn:nl:ui:32-325312 ; urn:nbn:nl:ui:32-325312 ; http://library.wur.nl/WebQuery/wurpubs/325312.

Council of Science Editors:

Kluskens LD. Molecular studies on protein- and carbohydrate-converting ezymes from thermophilic bacteria. [Doctoral Dissertation]. NARCIS; 2004. Available from: http://library.wur.nl/WebQuery/wurpubs/325312 ; urn:nbn:nl:ui:32-325312 ; urn:nbn:nl:ui:32-325312 ; http://library.wur.nl/WebQuery/wurpubs/325312


University of Cambridge

27. 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 17, 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. 17 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 17]. 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

28. 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 17, 2019. http://hdl.handle.net/2142/92923.

MLA Handbook (7th Edition):

Lambrecht, Michael. “The chemical and enzymatic synthesis of poly(ADP-ribose).” 2016. Web. 17 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 17]. 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

29. 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 17, 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. 17 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 17]. 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

30. 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 17, 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. 17 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 17]. 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

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