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You searched for subject:( 5 fluoro 5 deoxyribulose 1 phosphate). Showing records 1 – 30 of 33365 total matches.

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University of St. Andrews

1. Nasomjai, Pitak. Molecular probes for the evaluation of three isomerase enzyme mechanisms in secondary metabolism .

Degree: 2010, University of St. Andrews

 This thesis is focused on an investigation of the mechanisms of three enzymatically mediated carbon skeleton isomerisation reactions. Chapter 1 provides an overview of some… (more)

Subjects/Keywords: Isomerisation; Alkaloid; Cytochrome P450; Fluorometabolite; 5-fluoro-5-deoxyribulose-1-phosphate; Phostone; 2-C-methylerythitol-phophate-2-phosphate

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

APA (6th Edition):

Nasomjai, P. (2010). Molecular probes for the evaluation of three isomerase enzyme mechanisms in secondary metabolism . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/866

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

Chicago Manual of Style (16th Edition):

Nasomjai, Pitak. “Molecular probes for the evaluation of three isomerase enzyme mechanisms in secondary metabolism .” 2010. Thesis, University of St. Andrews. Accessed October 18, 2019. http://hdl.handle.net/10023/866.

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

MLA Handbook (7th Edition):

Nasomjai, Pitak. “Molecular probes for the evaluation of three isomerase enzyme mechanisms in secondary metabolism .” 2010. Web. 18 Oct 2019.

Vancouver:

Nasomjai P. Molecular probes for the evaluation of three isomerase enzyme mechanisms in secondary metabolism . [Internet] [Thesis]. University of St. Andrews; 2010. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10023/866.

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

Council of Science Editors:

Nasomjai P. Molecular probes for the evaluation of three isomerase enzyme mechanisms in secondary metabolism . [Thesis]. University of St. Andrews; 2010. Available from: http://hdl.handle.net/10023/866

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


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 October 18, 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. 18 Oct 2019.

Vancouver:

Lima S. Structure activity relationships in pyridoxal-5'-phosphate dependent enzymes. [Internet] [Doctoral dissertation]. University of Georgia; 2008. [cited 2019 Oct 18]. 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 South Florida

3. White, Justin K. Investigations into the Non-Mevalonate Isoprenoid Biosynthesis Pathway's First Two Enzymes utilizing Hybrid QM/MM Techniques.

Degree: 2017, University of South Florida

 Molecular drug design begins with the identication of a problem to solve. This work identies the growing resistance among human pathogens to current treatments. Once… (more)

Subjects/Keywords: QM/MM; computational; 1-Deoxy-D-xylulose 5-Phosphate Synthase; 1-Deoxy-D-xylulose 5-Phosphate Reductosiomerase; Biochemistry; Other Education

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APA (6th Edition):

White, J. K. (2017). Investigations into the Non-Mevalonate Isoprenoid Biosynthesis Pathway's First Two Enzymes utilizing Hybrid QM/MM Techniques. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/7107

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

Chicago Manual of Style (16th Edition):

White, Justin K. “Investigations into the Non-Mevalonate Isoprenoid Biosynthesis Pathway's First Two Enzymes utilizing Hybrid QM/MM Techniques.” 2017. Thesis, University of South Florida. Accessed October 18, 2019. https://scholarcommons.usf.edu/etd/7107.

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

MLA Handbook (7th Edition):

White, Justin K. “Investigations into the Non-Mevalonate Isoprenoid Biosynthesis Pathway's First Two Enzymes utilizing Hybrid QM/MM Techniques.” 2017. Web. 18 Oct 2019.

Vancouver:

White JK. Investigations into the Non-Mevalonate Isoprenoid Biosynthesis Pathway's First Two Enzymes utilizing Hybrid QM/MM Techniques. [Internet] [Thesis]. University of South Florida; 2017. [cited 2019 Oct 18]. Available from: https://scholarcommons.usf.edu/etd/7107.

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

Council of Science Editors:

White JK. Investigations into the Non-Mevalonate Isoprenoid Biosynthesis Pathway's First Two Enzymes utilizing Hybrid QM/MM Techniques. [Thesis]. University of South Florida; 2017. Available from: https://scholarcommons.usf.edu/etd/7107

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

4. 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 October 18, 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. 18 Oct 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 Oct 18]. 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


Virginia Tech

5. 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 October 18, 2019. http://hdl.handle.net/10919/50528.

MLA Handbook (7th Edition):

Liu, Pingyang. “Biochemical studies of enzymes in insect cuticle hardening.” 2013. Web. 18 Oct 2019.

Vancouver:

Liu P. Biochemical studies of enzymes in insect cuticle hardening. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Oct 18]. 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

6. 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 October 18, 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. 18 Oct 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 Oct 18]. 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

7. Kovac, Mitja. Fluoration de dérivés du benzovesamicol pour l'obtention de radioligands potentiels du transporteur vésiculaire de l'acéthylcholine : Synthesis and in vitro characterization of fluorinated benzovesamicol derivatives as potential radioligands for the vesicular acetylcholine transporter.

Degree: Docteur es, Pharmaceutical chemistry, 2013, Tours; Univerza v Ljubljani

Les déficiences en transporteur vésiculaire de l'acétylcholine (VAChT) sont l'un des symptômes précoces de perte neuronale lors de la maladie d'Alzheimer, perte fortement corrélée avec… (more)

Subjects/Keywords: VAChT; TEP; Benzovésamicol; Triazène; Fluorination; Alzheimer's disease; VAChT; PET; 5-FBVM; 5-TBV; Triazene; Fluoro-detriazenation

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APA (6th Edition):

Kovac, M. (2013). Fluoration de dérivés du benzovesamicol pour l'obtention de radioligands potentiels du transporteur vésiculaire de l'acéthylcholine : Synthesis and in vitro characterization of fluorinated benzovesamicol derivatives as potential radioligands for the vesicular acetylcholine transporter. (Doctoral Dissertation). Tours; Univerza v Ljubljani. Retrieved from http://www.theses.fr/2013TOUR3801

Chicago Manual of Style (16th Edition):

Kovac, Mitja. “Fluoration de dérivés du benzovesamicol pour l'obtention de radioligands potentiels du transporteur vésiculaire de l'acéthylcholine : Synthesis and in vitro characterization of fluorinated benzovesamicol derivatives as potential radioligands for the vesicular acetylcholine transporter.” 2013. Doctoral Dissertation, Tours; Univerza v Ljubljani. Accessed October 18, 2019. http://www.theses.fr/2013TOUR3801.

MLA Handbook (7th Edition):

Kovac, Mitja. “Fluoration de dérivés du benzovesamicol pour l'obtention de radioligands potentiels du transporteur vésiculaire de l'acéthylcholine : Synthesis and in vitro characterization of fluorinated benzovesamicol derivatives as potential radioligands for the vesicular acetylcholine transporter.” 2013. Web. 18 Oct 2019.

Vancouver:

Kovac M. Fluoration de dérivés du benzovesamicol pour l'obtention de radioligands potentiels du transporteur vésiculaire de l'acéthylcholine : Synthesis and in vitro characterization of fluorinated benzovesamicol derivatives as potential radioligands for the vesicular acetylcholine transporter. [Internet] [Doctoral dissertation]. Tours; Univerza v Ljubljani; 2013. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2013TOUR3801.

Council of Science Editors:

Kovac M. Fluoration de dérivés du benzovesamicol pour l'obtention de radioligands potentiels du transporteur vésiculaire de l'acéthylcholine : Synthesis and in vitro characterization of fluorinated benzovesamicol derivatives as potential radioligands for the vesicular acetylcholine transporter. [Doctoral Dissertation]. Tours; Univerza v Ljubljani; 2013. Available from: http://www.theses.fr/2013TOUR3801


University of Michigan

8. Hagena, Tara Lynn. Selenium-Containing Glycosides and Glycosyl Phosphates as Precursors of Glycosyl Epoxides: New Approaches to the Synthesis of (5-Fluoro) and (5-Cyano) Glycosides.

Degree: PhD, Chemistry, 2008, University of Michigan

 ABSTRACT Enzyme-catalyzed transformations of carbohydrates proceed through different transition states, which may be studied by altering the electron density at various positions of the carbohydrate… (more)

Subjects/Keywords: (5-fluoro) Glycosides; (5-cyano) Glycosides; Chemistry; Science

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APA (6th Edition):

Hagena, T. L. (2008). Selenium-Containing Glycosides and Glycosyl Phosphates as Precursors of Glycosyl Epoxides: New Approaches to the Synthesis of (5-Fluoro) and (5-Cyano) Glycosides. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/58513

Chicago Manual of Style (16th Edition):

Hagena, Tara Lynn. “Selenium-Containing Glycosides and Glycosyl Phosphates as Precursors of Glycosyl Epoxides: New Approaches to the Synthesis of (5-Fluoro) and (5-Cyano) Glycosides.” 2008. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/58513.

MLA Handbook (7th Edition):

Hagena, Tara Lynn. “Selenium-Containing Glycosides and Glycosyl Phosphates as Precursors of Glycosyl Epoxides: New Approaches to the Synthesis of (5-Fluoro) and (5-Cyano) Glycosides.” 2008. Web. 18 Oct 2019.

Vancouver:

Hagena TL. Selenium-Containing Glycosides and Glycosyl Phosphates as Precursors of Glycosyl Epoxides: New Approaches to the Synthesis of (5-Fluoro) and (5-Cyano) Glycosides. [Internet] [Doctoral dissertation]. University of Michigan; 2008. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/58513.

Council of Science Editors:

Hagena TL. Selenium-Containing Glycosides and Glycosyl Phosphates as Precursors of Glycosyl Epoxides: New Approaches to the Synthesis of (5-Fluoro) and (5-Cyano) Glycosides. [Doctoral Dissertation]. University of Michigan; 2008. Available from: http://hdl.handle.net/2027.42/58513


Virginia Tech

9. 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 October 18, 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. 18 Oct 2019.

Vancouver:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Oct 18]. 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 South Florida

10. Handa, Sumit. 1-deoxy-D-xylulose-5-phosphate Synthase (DXS) Mechanistic Study and its Implication in the Development of Novel Antibiotics and Antimalarials.

Degree: 2012, University of South Florida

 Isoprenoids are the largest family of biologically active compounds, synthesized by five carbon subunits namely isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP). For long time… (more)

Subjects/Keywords: 1-deoxy-D-xylulose-5-phosphate Synthase; D. radiodurans; non mevalonate pathway; P. vivax; American Studies; Arts and Humanities; Biochemistry

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APA (6th Edition):

Handa, S. (2012). 1-deoxy-D-xylulose-5-phosphate Synthase (DXS) Mechanistic Study and its Implication in the Development of Novel Antibiotics and Antimalarials. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4063

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

Chicago Manual of Style (16th Edition):

Handa, Sumit. “1-deoxy-D-xylulose-5-phosphate Synthase (DXS) Mechanistic Study and its Implication in the Development of Novel Antibiotics and Antimalarials.” 2012. Thesis, University of South Florida. Accessed October 18, 2019. https://scholarcommons.usf.edu/etd/4063.

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

MLA Handbook (7th Edition):

Handa, Sumit. “1-deoxy-D-xylulose-5-phosphate Synthase (DXS) Mechanistic Study and its Implication in the Development of Novel Antibiotics and Antimalarials.” 2012. Web. 18 Oct 2019.

Vancouver:

Handa S. 1-deoxy-D-xylulose-5-phosphate Synthase (DXS) Mechanistic Study and its Implication in the Development of Novel Antibiotics and Antimalarials. [Internet] [Thesis]. University of South Florida; 2012. [cited 2019 Oct 18]. Available from: https://scholarcommons.usf.edu/etd/4063.

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

Council of Science Editors:

Handa S. 1-deoxy-D-xylulose-5-phosphate Synthase (DXS) Mechanistic Study and its Implication in the Development of Novel Antibiotics and Antimalarials. [Thesis]. University of South Florida; 2012. Available from: https://scholarcommons.usf.edu/etd/4063

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

11. 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 October 18, 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. 18 Oct 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 Oct 18]. 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

12. Stojanovski, Bosko M. 5-Aminolevulinate Synthase: Characterization of the Enzymatic Mechanism, Reaction Selectivity, and Structural Plasticity.

Degree: 2015, University of South Florida

5-Aminolevulinate synthase (ALAS) catalyzes the pyridoxal 5'-phosphate (PLP)-dependent condensation between glycine and succinyl-CoA to generate coenzyme A (CoA), CO2, and 5-aminolevulinate (ALA). The chemical mechanism… (more)

Subjects/Keywords: 5-Aminolevulinate synthase; heme; pyridoxal 5’-phosphate; enzyme mechanisms; molten globule; Medicine and Health Sciences

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APA (6th Edition):

Stojanovski, B. M. (2015). 5-Aminolevulinate Synthase: Characterization of the Enzymatic Mechanism, Reaction Selectivity, and Structural Plasticity. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5879

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

Chicago Manual of Style (16th Edition):

Stojanovski, Bosko M. “5-Aminolevulinate Synthase: Characterization of the Enzymatic Mechanism, Reaction Selectivity, and Structural Plasticity.” 2015. Thesis, University of South Florida. Accessed October 18, 2019. https://scholarcommons.usf.edu/etd/5879.

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

MLA Handbook (7th Edition):

Stojanovski, Bosko M. “5-Aminolevulinate Synthase: Characterization of the Enzymatic Mechanism, Reaction Selectivity, and Structural Plasticity.” 2015. Web. 18 Oct 2019.

Vancouver:

Stojanovski BM. 5-Aminolevulinate Synthase: Characterization of the Enzymatic Mechanism, Reaction Selectivity, and Structural Plasticity. [Internet] [Thesis]. University of South Florida; 2015. [cited 2019 Oct 18]. Available from: https://scholarcommons.usf.edu/etd/5879.

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

Council of Science Editors:

Stojanovski BM. 5-Aminolevulinate Synthase: Characterization of the Enzymatic Mechanism, Reaction Selectivity, and Structural Plasticity. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5879

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


University of Alberta

13. 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 October 18, 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. 18 Oct 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 Oct 18]. 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

14. 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 October 18, 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. 18 Oct 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 Oct 18]. 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

15. 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 October 18, 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. 18 Oct 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 Oct 18]. 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

16. Chatham, Laura. Examination of target-site-based mechanisms of glyphosate resistance in waterhemp (Amaranthus tuberculatus).

Degree: MS, 0030, 2014, University of Illinois – Urbana-Champaign

 Glyphosate is one of the most important and widely used herbicide in the world. While few weed species had evolved resistance in the two decades… (more)

Subjects/Keywords: glyphosate resistance; waterhemp; 5-enolpyruvylshikimate-3-phosphate (EPSPS) gene amplification

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APA (6th Edition):

Chatham, L. (2014). Examination of target-site-based mechanisms of glyphosate resistance in waterhemp (Amaranthus tuberculatus). (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50644

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

Chicago Manual of Style (16th Edition):

Chatham, Laura. “Examination of target-site-based mechanisms of glyphosate resistance in waterhemp (Amaranthus tuberculatus).” 2014. Thesis, University of Illinois – Urbana-Champaign. Accessed October 18, 2019. http://hdl.handle.net/2142/50644.

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

MLA Handbook (7th Edition):

Chatham, Laura. “Examination of target-site-based mechanisms of glyphosate resistance in waterhemp (Amaranthus tuberculatus).” 2014. Web. 18 Oct 2019.

Vancouver:

Chatham L. Examination of target-site-based mechanisms of glyphosate resistance in waterhemp (Amaranthus tuberculatus). [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2142/50644.

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

Council of Science Editors:

Chatham L. Examination of target-site-based mechanisms of glyphosate resistance in waterhemp (Amaranthus tuberculatus). [Thesis]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50644

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


Georgia State University

17. Klenc, Jeffrey D. Design and Synthesis of Novel Serotonin Receptor Ligands.

Degree: PhD, Chemistry, 2010, Georgia State University

  Novel and potent ligands to the serotonin7 (5-HT7) receptor have been synthesized. The synthesized compounds include a set of substituted pyrimidines which show high… (more)

Subjects/Keywords: Serotonin; 5-HT; Depression; Schizophrenia; Pyrimidine; 1-4 Addition; 3D-QSAR; Molecular modeling; 5-HT7 receptor; 5-HT7 ligands; 5-HT1a; 5-HT2a; Pharmacophore; Chemistry

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APA (6th Edition):

Klenc, J. D. (2010). Design and Synthesis of Novel Serotonin Receptor Ligands. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/50

Chicago Manual of Style (16th Edition):

Klenc, Jeffrey D. “Design and Synthesis of Novel Serotonin Receptor Ligands.” 2010. Doctoral Dissertation, Georgia State University. Accessed October 18, 2019. https://scholarworks.gsu.edu/chemistry_diss/50.

MLA Handbook (7th Edition):

Klenc, Jeffrey D. “Design and Synthesis of Novel Serotonin Receptor Ligands.” 2010. Web. 18 Oct 2019.

Vancouver:

Klenc JD. Design and Synthesis of Novel Serotonin Receptor Ligands. [Internet] [Doctoral dissertation]. Georgia State University; 2010. [cited 2019 Oct 18]. Available from: https://scholarworks.gsu.edu/chemistry_diss/50.

Council of Science Editors:

Klenc JD. Design and Synthesis of Novel Serotonin Receptor Ligands. [Doctoral Dissertation]. Georgia State University; 2010. Available from: https://scholarworks.gsu.edu/chemistry_diss/50


Universidade Federal de Santa Maria

18. Sandra Vanderli Mayer-Winkelmann. DISTRIBUIÇÃO DO DNA DOS HERPESVÍRUS BOVINO TIPOS 1 (BHV-1) E 5 (BHV-5) NO ENCÉFALO DE COELHOS DURANTE A INFECÇÃO LATENTE.

Degree: 2005, Universidade Federal de Santa Maria

O herpesvírus bovino tipo 5 (BHV-5) é um importante agente etiológico de meningoencefalite em bovinos e estabelece infecção latente em seus hospedeiros, principalmente nos gânglios… (more)

Subjects/Keywords: herpesvírus bovino tipos 1 e 5; BHV-5; BHV-1; infecção latente; coelhos; MEDICINA VETERINARIA; bovine herpesvirus type 5; BHV-5; BHV-1; latent infection; rabbits

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APA (6th Edition):

Mayer-Winkelmann, S. V. (2005). DISTRIBUIÇÃO DO DNA DOS HERPESVÍRUS BOVINO TIPOS 1 (BHV-1) E 5 (BHV-5) NO ENCÉFALO DE COELHOS DURANTE A INFECÇÃO LATENTE. (Thesis). Universidade Federal de Santa Maria. Retrieved from http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=1550

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

Chicago Manual of Style (16th Edition):

Mayer-Winkelmann, Sandra Vanderli. “DISTRIBUIÇÃO DO DNA DOS HERPESVÍRUS BOVINO TIPOS 1 (BHV-1) E 5 (BHV-5) NO ENCÉFALO DE COELHOS DURANTE A INFECÇÃO LATENTE.” 2005. Thesis, Universidade Federal de Santa Maria. Accessed October 18, 2019. http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=1550.

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

MLA Handbook (7th Edition):

Mayer-Winkelmann, Sandra Vanderli. “DISTRIBUIÇÃO DO DNA DOS HERPESVÍRUS BOVINO TIPOS 1 (BHV-1) E 5 (BHV-5) NO ENCÉFALO DE COELHOS DURANTE A INFECÇÃO LATENTE.” 2005. Web. 18 Oct 2019.

Vancouver:

Mayer-Winkelmann SV. DISTRIBUIÇÃO DO DNA DOS HERPESVÍRUS BOVINO TIPOS 1 (BHV-1) E 5 (BHV-5) NO ENCÉFALO DE COELHOS DURANTE A INFECÇÃO LATENTE. [Internet] [Thesis]. Universidade Federal de Santa Maria; 2005. [cited 2019 Oct 18]. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=1550.

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

Council of Science Editors:

Mayer-Winkelmann SV. DISTRIBUIÇÃO DO DNA DOS HERPESVÍRUS BOVINO TIPOS 1 (BHV-1) E 5 (BHV-5) NO ENCÉFALO DE COELHOS DURANTE A INFECÇÃO LATENTE. [Thesis]. Universidade Federal de Santa Maria; 2005. Available from: http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=1550

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


University of Otago

19. Chavani, Ottiniel. Development, validation and application of a liquid chromatography tandem mass spectrometry assay for uracil and 5,6-dihydrouracil along with 5-fluorouracil and its metabolites, in human plasma .

Degree: University of Otago

5-Fluorouracil (5-FU), a pyrimidine analogue, is one of the commonly prescribed chemotherapeutic drugs for solid tumours, principally of the digestive tract, breast plus head and… (more)

Subjects/Keywords: uracil; 5,6-dihydrouracil; 5,6-dihydrouracil/uracil ratio; 5-fluorouracil; 5-fluoro-5,6-dihydrouracil; α-fluoro-β-ureidopropionic acid; α-fluoro-β-alanine; therapeutic drug monitoring; 5-FU response prediction; 5-FU toxicity prediction

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

APA (6th Edition):

Chavani, O. (n.d.). Development, validation and application of a liquid chromatography tandem mass spectrometry assay for uracil and 5,6-dihydrouracil along with 5-fluorouracil and its metabolites, in human plasma . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/7431

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Chicago Manual of Style (16th Edition):

Chavani, Ottiniel. “Development, validation and application of a liquid chromatography tandem mass spectrometry assay for uracil and 5,6-dihydrouracil along with 5-fluorouracil and its metabolites, in human plasma .” Masters Thesis, University of Otago. Accessed October 18, 2019. http://hdl.handle.net/10523/7431.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

MLA Handbook (7th Edition):

Chavani, Ottiniel. “Development, validation and application of a liquid chromatography tandem mass spectrometry assay for uracil and 5,6-dihydrouracil along with 5-fluorouracil and its metabolites, in human plasma .” Web. 18 Oct 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Chavani O. Development, validation and application of a liquid chromatography tandem mass spectrometry assay for uracil and 5,6-dihydrouracil along with 5-fluorouracil and its metabolites, in human plasma . [Internet] [Masters thesis]. University of Otago; [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10523/7431.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Council of Science Editors:

Chavani O. Development, validation and application of a liquid chromatography tandem mass spectrometry assay for uracil and 5,6-dihydrouracil along with 5-fluorouracil and its metabolites, in human plasma . [Masters Thesis]. University of Otago; Available from: http://hdl.handle.net/10523/7431

Note: this citation may be lacking information needed for this citation format:
No year of publication.

20. Agustoni, Camila de Almeida. Influência do polimorfismo do gene do CCR-5 na transmissão materno-infantil do HIV-1.

Degree: Mestrado, Enfermagem Fundamental, 2011, University of São Paulo

A principal via de infecção pelo Vírus da Imunodeficiência Humana (HIV-1) em crianças é a transmissão materno-infantil (TMI). Diversos fatores podem estar associados com a… (more)

Subjects/Keywords: CCR-5; CCR-5; HIV; HIV-1; maternal-infant transmission (MIT); transmissão materno-infantil (TMI)

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APA (6th Edition):

Agustoni, C. d. A. (2011). Influência do polimorfismo do gene do CCR-5 na transmissão materno-infantil do HIV-1. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/22/22132/tde-28112011-081634/ ;

Chicago Manual of Style (16th Edition):

Agustoni, Camila de Almeida. “Influência do polimorfismo do gene do CCR-5 na transmissão materno-infantil do HIV-1.” 2011. Masters Thesis, University of São Paulo. Accessed October 18, 2019. http://www.teses.usp.br/teses/disponiveis/22/22132/tde-28112011-081634/ ;.

MLA Handbook (7th Edition):

Agustoni, Camila de Almeida. “Influência do polimorfismo do gene do CCR-5 na transmissão materno-infantil do HIV-1.” 2011. Web. 18 Oct 2019.

Vancouver:

Agustoni CdA. Influência do polimorfismo do gene do CCR-5 na transmissão materno-infantil do HIV-1. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2019 Oct 18]. Available from: http://www.teses.usp.br/teses/disponiveis/22/22132/tde-28112011-081634/ ;.

Council of Science Editors:

Agustoni CdA. Influência do polimorfismo do gene do CCR-5 na transmissão materno-infantil do HIV-1. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/22/22132/tde-28112011-081634/ ;

21. Aono, Riku. Studies on nucleotide and pentose metabolism in Archaea : アーキアにおける核酸およびペントース代謝に関する研究.

Degree: 博士(工学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第19188号

工博第4065号

Subjects/Keywords: Archaea; nucleoside; nucleoside phosphorylase; pentose bisphosphate pathway; ADP-dependent ribose-1-phosphate kinase; ribose-1, 5-bisphosphate isomerase; ribulose-1, 5-bisphosphate carboxylase/oxygenase

Page 1 Page 2 Page 3 Page 4

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APA (6th Edition):

Aono, R. (2015). Studies on nucleotide and pentose metabolism in Archaea : アーキアにおける核酸およびペントース代謝に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/200451 ; http://dx.doi.org/10.14989/doctor.k19188

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

Chicago Manual of Style (16th Edition):

Aono, Riku. “Studies on nucleotide and pentose metabolism in Archaea : アーキアにおける核酸およびペントース代謝に関する研究.” 2015. Thesis, Kyoto University / 京都大学. Accessed October 18, 2019. http://hdl.handle.net/2433/200451 ; http://dx.doi.org/10.14989/doctor.k19188.

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

MLA Handbook (7th Edition):

Aono, Riku. “Studies on nucleotide and pentose metabolism in Archaea : アーキアにおける核酸およびペントース代謝に関する研究.” 2015. Web. 18 Oct 2019.

Vancouver:

Aono R. Studies on nucleotide and pentose metabolism in Archaea : アーキアにおける核酸およびペントース代謝に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2433/200451 ; http://dx.doi.org/10.14989/doctor.k19188.

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

Council of Science Editors:

Aono R. Studies on nucleotide and pentose metabolism in Archaea : アーキアにおける核酸およびペントース代謝に関する研究. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/200451 ; http://dx.doi.org/10.14989/doctor.k19188

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


Kyoto University

22. Aono, Riku. Studies on nucleotide and pentose metabolism in Archaea .

Degree: 2015, Kyoto University

Subjects/Keywords: Archaea; nucleoside; nucleoside phosphorylase; pentose bisphosphate pathway; ADP-dependent ribose-1-phosphate kinase; ribose-1, 5-bisphosphate isomerase; ribulose-1, 5-bisphosphate carboxylase/oxygenase

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

APA (6th Edition):

Aono, R. (2015). Studies on nucleotide and pentose metabolism in Archaea . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/200451

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

Chicago Manual of Style (16th Edition):

Aono, Riku. “Studies on nucleotide and pentose metabolism in Archaea .” 2015. Thesis, Kyoto University. Accessed October 18, 2019. http://hdl.handle.net/2433/200451.

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

MLA Handbook (7th Edition):

Aono, Riku. “Studies on nucleotide and pentose metabolism in Archaea .” 2015. Web. 18 Oct 2019.

Vancouver:

Aono R. Studies on nucleotide and pentose metabolism in Archaea . [Internet] [Thesis]. Kyoto University; 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2433/200451.

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

Council of Science Editors:

Aono R. Studies on nucleotide and pentose metabolism in Archaea . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/200451

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


University of Alberta

23. 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 October 18, 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. 18 Oct 2019.

Vancouver:

Watanabe N. LL-diaminopimelate aminotransferase: the mechanism of substrate recognition and specificity. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2019 Oct 18]. 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 Alberta

24. Nish, Gordon L. Optimization of the reaction conditions of two enzymes for use in a carbon sequestration process, and investigation into immobilization via encapsulation within polymersomes.

Degree: MS, Department of Chemical and Materials Engineering, 2016, University of Alberta

 Carbon dioxide emissions from human activities contribute to an increase of greenhouse gases in the atmosphere. In nature, this gas is sequestered through the use… (more)

Subjects/Keywords: polymersome; phosphoribulokinase; optimization; ribose 5-phosphate isomerase; encapsulation; immobilization; enzyme; carbon capture

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APA (6th Edition):

Nish, G. L. (2016). Optimization of the reaction conditions of two enzymes for use in a carbon sequestration process, and investigation into immobilization via encapsulation within polymersomes. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cv405s966t

Chicago Manual of Style (16th Edition):

Nish, Gordon L. “Optimization of the reaction conditions of two enzymes for use in a carbon sequestration process, and investigation into immobilization via encapsulation within polymersomes.” 2016. Masters Thesis, University of Alberta. Accessed October 18, 2019. https://era.library.ualberta.ca/files/cv405s966t.

MLA Handbook (7th Edition):

Nish, Gordon L. “Optimization of the reaction conditions of two enzymes for use in a carbon sequestration process, and investigation into immobilization via encapsulation within polymersomes.” 2016. Web. 18 Oct 2019.

Vancouver:

Nish GL. Optimization of the reaction conditions of two enzymes for use in a carbon sequestration process, and investigation into immobilization via encapsulation within polymersomes. [Internet] [Masters thesis]. University of Alberta; 2016. [cited 2019 Oct 18]. Available from: https://era.library.ualberta.ca/files/cv405s966t.

Council of Science Editors:

Nish GL. Optimization of the reaction conditions of two enzymes for use in a carbon sequestration process, and investigation into immobilization via encapsulation within polymersomes. [Masters Thesis]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/cv405s966t


University of Manchester

25. 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 October 18, 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. 18 Oct 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 Oct 18]. 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

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

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 October 18, 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. 18 Oct 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 Oct 18]. 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


University of Wisconsin – Milwaukee

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

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 October 18, 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. 18 Oct 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 Oct 18]. 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 Guelph

28. Jeffery, Taylor. Investigation into the Molecular and Biochemical Mechanisms of Resistance in Two Biotypes of Glyphosate Resistant Giant Ragweed .

Degree: 2014, University of Guelph

 Glyphosate resistant giant ragweed poses a significant threat to farmers in southern Ontario as interference from this species can result in massive yield loses. The… (more)

Subjects/Keywords: Giant Ragweed; Ambrosia trifida; EPSPS; 5-enolpyruvylshikimate-3-phosphate synthase; glycolate oxidase; glyoxylate; H2O2

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APA (6th Edition):

Jeffery, T. (2014). Investigation into the Molecular and Biochemical Mechanisms of Resistance in Two Biotypes of Glyphosate Resistant Giant Ragweed . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8627

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

Chicago Manual of Style (16th Edition):

Jeffery, Taylor. “Investigation into the Molecular and Biochemical Mechanisms of Resistance in Two Biotypes of Glyphosate Resistant Giant Ragweed .” 2014. Thesis, University of Guelph. Accessed October 18, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8627.

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

MLA Handbook (7th Edition):

Jeffery, Taylor. “Investigation into the Molecular and Biochemical Mechanisms of Resistance in Two Biotypes of Glyphosate Resistant Giant Ragweed .” 2014. Web. 18 Oct 2019.

Vancouver:

Jeffery T. Investigation into the Molecular and Biochemical Mechanisms of Resistance in Two Biotypes of Glyphosate Resistant Giant Ragweed . [Internet] [Thesis]. University of Guelph; 2014. [cited 2019 Oct 18]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8627.

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

Council of Science Editors:

Jeffery T. Investigation into the Molecular and Biochemical Mechanisms of Resistance in Two Biotypes of Glyphosate Resistant Giant Ragweed . [Thesis]. University of Guelph; 2014. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8627

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


Universidade de Lisboa

29. Ramos, Rúben José Jesus Faustino. Pentose phosphate pathway in health and disease: from metabolic dysfunction to biomarkers.

Degree: 2013, Universidade de Lisboa

Tese de mestrado, Análises Clínicas, Universidade de Lisboa, Faculdade de Farmácia, 2013

The Pentose Phosphate Pathway (PPP) fulfils two unique functions: (i) the formation of… (more)

Subjects/Keywords: Pentose Phosphate Pathway; Ribose-5-phosphate isomerase deficiency; Transaldolase deficiency; Non-alcoholic fatty liver disease; Sedoheptulokinase deficiency; Teses de mestrado - 2013

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APA (6th Edition):

Ramos, R. J. J. F. (2013). Pentose phosphate pathway in health and disease: from metabolic dysfunction to biomarkers. (Thesis). Universidade de Lisboa. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/11353

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

Chicago Manual of Style (16th Edition):

Ramos, Rúben José Jesus Faustino. “Pentose phosphate pathway in health and disease: from metabolic dysfunction to biomarkers.” 2013. Thesis, Universidade de Lisboa. Accessed October 18, 2019. http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/11353.

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

MLA Handbook (7th Edition):

Ramos, Rúben José Jesus Faustino. “Pentose phosphate pathway in health and disease: from metabolic dysfunction to biomarkers.” 2013. Web. 18 Oct 2019.

Vancouver:

Ramos RJJF. Pentose phosphate pathway in health and disease: from metabolic dysfunction to biomarkers. [Internet] [Thesis]. Universidade de Lisboa; 2013. [cited 2019 Oct 18]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/11353.

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

Council of Science Editors:

Ramos RJJF. Pentose phosphate pathway in health and disease: from metabolic dysfunction to biomarkers. [Thesis]. Universidade de Lisboa; 2013. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/11353

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


Virginia Tech

30. Sun, Fangfang. Development of Building Blocks - Thermostable Enzymes for Synthetic Pathway Biotransformation (SyPaB).

Degree: MS, Biological Systems Engineering, 2012, Virginia Tech

 Hydrogen production from abundant renewable biomass would decrease reliance on crude oils, achieve nearly zero net greenhouse gas emissions, create more jobs, and enhance national… (more)

Subjects/Keywords: substrate channeling; synthetic pathway biotranformation (SyPaB); diaphorase; glucose-6-phosphate dehydrogenase; RpiB; ribose-5-phosphate isomerase; thermostable enzymes; biofuel

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

APA (6th Edition):

Sun, F. (2012). Development of Building Blocks - Thermostable Enzymes for Synthetic Pathway Biotransformation (SyPaB). (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77009

Chicago Manual of Style (16th Edition):

Sun, Fangfang. “Development of Building Blocks - Thermostable Enzymes for Synthetic Pathway Biotransformation (SyPaB).” 2012. Masters Thesis, Virginia Tech. Accessed October 18, 2019. http://hdl.handle.net/10919/77009.

MLA Handbook (7th Edition):

Sun, Fangfang. “Development of Building Blocks - Thermostable Enzymes for Synthetic Pathway Biotransformation (SyPaB).” 2012. Web. 18 Oct 2019.

Vancouver:

Sun F. Development of Building Blocks - Thermostable Enzymes for Synthetic Pathway Biotransformation (SyPaB). [Internet] [Masters thesis]. Virginia Tech; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10919/77009.

Council of Science Editors:

Sun F. Development of Building Blocks - Thermostable Enzymes for Synthetic Pathway Biotransformation (SyPaB). [Masters Thesis]. Virginia Tech; 2012. Available from: http://hdl.handle.net/10919/77009

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