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You searched for subject:(PQQ ABH NGIGE ALKOHOLDEHYDROGENASE ENZYME ). Showing records 1 – 30 of 3191 total matches.

[1] [2] [3] [4] [5] … [107]

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ETH Zürich

1. Schmidt, Sabrina. Functional investigation of methanol dehydrogenase-like protein XoxF in Methylobacterium extorquens AM1.

Degree: 2010, ETH Zürich

Subjects/Keywords: METHYLOBACTERIUM (MIKROBIOLOGIE); PQQ-ABHÄNGIGE ALKOHOLDEHYDROGENASE (ENZYME); FUNKTIONELLE UNTERTEILUNGEN + KOMPARTIMENTIERUNG + POOLS (BIOLOGIE); PROTEINFUNKTION + PEPTIDFUNKTION; METHYLOBACTERIUM (MICROBIOLOGY); PQQ DEPENDENT ALCOHOL DEHYDROGENASE (ENZYMES); FUNCTIONAL PARTS + COMPARTMENTS + POOLS (BIOLOGY); PROTEIN FUNCTION + PEPTIDE FUNCTION; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Schmidt, S. (2010). Functional investigation of methanol dehydrogenase-like protein XoxF in Methylobacterium extorquens AM1. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152312

Chicago Manual of Style (16th Edition):

Schmidt, Sabrina. “Functional investigation of methanol dehydrogenase-like protein XoxF in Methylobacterium extorquens AM1.” 2010. Doctoral Dissertation, ETH Zürich. Accessed October 28, 2020. http://hdl.handle.net/20.500.11850/152312.

MLA Handbook (7th Edition):

Schmidt, Sabrina. “Functional investigation of methanol dehydrogenase-like protein XoxF in Methylobacterium extorquens AM1.” 2010. Web. 28 Oct 2020.

Vancouver:

Schmidt S. Functional investigation of methanol dehydrogenase-like protein XoxF in Methylobacterium extorquens AM1. [Internet] [Doctoral dissertation]. ETH Zürich; 2010. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/20.500.11850/152312.

Council of Science Editors:

Schmidt S. Functional investigation of methanol dehydrogenase-like protein XoxF in Methylobacterium extorquens AM1. [Doctoral Dissertation]. ETH Zürich; 2010. Available from: http://hdl.handle.net/20.500.11850/152312


ETH Zürich

2. Müller, Jonas Ernst Norbert. Development of strategies to enable Escherichia coli to utilize methanol as a substrate based on findings in Bacillus methanolicus.

Degree: 2014, ETH Zürich

Subjects/Keywords: ESCHERICHIA (MIKROBIOLOGIE); METHYLOTROPHIE + METHYLOTROPHE MIKROORGANISMEN (MIKROBIOLOGIE); TRANSGENE MIKROORGANISMEN + GENETISCH MANIPULIERTE MIKROORGANISMEN; PQQ-ABHÄNGIGE ALKOHOLDEHYDROGENASE (ENZYME); HETEROLOGE GENEXPRESSION, EXPRESSION VON FREMDGENEN (GENETIK); ESCHERICHIA (MICROBIOLOGY); METHYLOTROPHY + METHYLOTROPHIC MICROORGANISMS (MICROBIOLOGY); TRANSGENIC MICROORGANISMS + GENETICALLY ENGINEERED MICROORGANISMS; PQQ DEPENDENT ALCOHOL DEHYDROGENASE (ENZYMES); HETEROLOGOUS GENE EXPRESSION + EXPRESSION OF FOREIGN GENES (GENETICS); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Müller, J. E. N. (2014). Development of strategies to enable Escherichia coli to utilize methanol as a substrate based on findings in Bacillus methanolicus. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/154831

Chicago Manual of Style (16th Edition):

Müller, Jonas Ernst Norbert. “Development of strategies to enable Escherichia coli to utilize methanol as a substrate based on findings in Bacillus methanolicus.” 2014. Doctoral Dissertation, ETH Zürich. Accessed October 28, 2020. http://hdl.handle.net/20.500.11850/154831.

MLA Handbook (7th Edition):

Müller, Jonas Ernst Norbert. “Development of strategies to enable Escherichia coli to utilize methanol as a substrate based on findings in Bacillus methanolicus.” 2014. Web. 28 Oct 2020.

Vancouver:

Müller JEN. Development of strategies to enable Escherichia coli to utilize methanol as a substrate based on findings in Bacillus methanolicus. [Internet] [Doctoral dissertation]. ETH Zürich; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/20.500.11850/154831.

Council of Science Editors:

Müller JEN. Development of strategies to enable Escherichia coli to utilize methanol as a substrate based on findings in Bacillus methanolicus. [Doctoral Dissertation]. ETH Zürich; 2014. Available from: http://hdl.handle.net/20.500.11850/154831


University of Michigan

3. Zimmerman, Laura B. Pyrroloquinoline Quinone (PQQ) Labeling Moieties for the Sensitive Detection of Biomolecules.

Degree: PhD, Chemistry, 2010, University of Michigan

 Since the development of the immunoassay, biomolecule detection via binding assays has become vitally important in many fields. High sensitivity in such assays usually requires… (more)

Subjects/Keywords: Pyrroloquinoline Quinone (PQQ); Biomolecule Detection; Optical Assay; Enzyme Reconstitution; Chemistry; Science

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APA (6th Edition):

Zimmerman, L. B. (2010). Pyrroloquinoline Quinone (PQQ) Labeling Moieties for the Sensitive Detection of Biomolecules. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/77822

Chicago Manual of Style (16th Edition):

Zimmerman, Laura B. “Pyrroloquinoline Quinone (PQQ) Labeling Moieties for the Sensitive Detection of Biomolecules.” 2010. Doctoral Dissertation, University of Michigan. Accessed October 28, 2020. http://hdl.handle.net/2027.42/77822.

MLA Handbook (7th Edition):

Zimmerman, Laura B. “Pyrroloquinoline Quinone (PQQ) Labeling Moieties for the Sensitive Detection of Biomolecules.” 2010. Web. 28 Oct 2020.

Vancouver:

Zimmerman LB. Pyrroloquinoline Quinone (PQQ) Labeling Moieties for the Sensitive Detection of Biomolecules. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2027.42/77822.

Council of Science Editors:

Zimmerman LB. Pyrroloquinoline Quinone (PQQ) Labeling Moieties for the Sensitive Detection of Biomolecules. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/77822


University of California – Berkeley

4. RoseFigura, Jordan M. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.

Degree: Chemistry, 2010, University of California – Berkeley

PQQ is an exogenous, tricyclic, quino-cofactor for a number of bacterial dehydrogenase reaction. It has also been proposed to play a role as a bacterial… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; Oxygen activation; PQQ

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APA (6th Edition):

RoseFigura, J. M. (2010). Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4jh004zw

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):

RoseFigura, Jordan M. “Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.” 2010. Thesis, University of California – Berkeley. Accessed October 28, 2020. http://www.escholarship.org/uc/item/4jh004zw.

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

MLA Handbook (7th Edition):

RoseFigura, Jordan M. “Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.” 2010. Web. 28 Oct 2020.

Vancouver:

RoseFigura JM. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2020 Oct 28]. Available from: http://www.escholarship.org/uc/item/4jh004zw.

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

Council of Science Editors:

RoseFigura JM. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/4jh004zw

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


University of Kentucky

5. An, Ran. STUDIES ON REGULATION OF PQQ-DEPENDENT PHOSPHATE SOLUBILIZATION AMONG RHIZOSPHERE DWELLING BACTERIA.

Degree: 2016, University of Kentucky

 Plant growth promotion can be enhanced by soil- and rhizosphere-dwelling bacteria by a several different methods. One method is by promoting nutrient acquisition from soil.… (more)

Subjects/Keywords: Phosphate solubilization; PQQ; Glucose dehydrogenase; pqq operon structure; Environmental Microbiology and Microbial Ecology

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APA (6th Edition):

An, R. (2016). STUDIES ON REGULATION OF PQQ-DEPENDENT PHOSPHATE SOLUBILIZATION AMONG RHIZOSPHERE DWELLING BACTERIA. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pss_etds/79

Chicago Manual of Style (16th Edition):

An, Ran. “STUDIES ON REGULATION OF PQQ-DEPENDENT PHOSPHATE SOLUBILIZATION AMONG RHIZOSPHERE DWELLING BACTERIA.” 2016. Doctoral Dissertation, University of Kentucky. Accessed October 28, 2020. https://uknowledge.uky.edu/pss_etds/79.

MLA Handbook (7th Edition):

An, Ran. “STUDIES ON REGULATION OF PQQ-DEPENDENT PHOSPHATE SOLUBILIZATION AMONG RHIZOSPHERE DWELLING BACTERIA.” 2016. Web. 28 Oct 2020.

Vancouver:

An R. STUDIES ON REGULATION OF PQQ-DEPENDENT PHOSPHATE SOLUBILIZATION AMONG RHIZOSPHERE DWELLING BACTERIA. [Internet] [Doctoral dissertation]. University of Kentucky; 2016. [cited 2020 Oct 28]. Available from: https://uknowledge.uky.edu/pss_etds/79.

Council of Science Editors:

An R. STUDIES ON REGULATION OF PQQ-DEPENDENT PHOSPHATE SOLUBILIZATION AMONG RHIZOSPHERE DWELLING BACTERIA. [Doctoral Dissertation]. University of Kentucky; 2016. Available from: https://uknowledge.uky.edu/pss_etds/79

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

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

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

Subjects/Keywords: Enzyme

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Mayol, Ombeline. “Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed October 28, 2020. http://www.theses.fr/2018SACLE026.

MLA Handbook (7th Edition):

Mayol, Ombeline. “Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution.” 2018. Web. 28 Oct 2020.

Vancouver:

Mayol O. Amine déshydrogénases pour la synthèse biocatalysée d’amines chirales : recherche, application et évolution : Amine dehydrogenases for biocatalytic synthesis of chiral amines : discovery, application and evolution. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2018SACLE026.

Council of Science Editors:

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


North Carolina State University

7. Sullivan, Daniel Michael. Molecular and Structural Characterization of Proteins Involved in Bacterial Adaptive Responses.

Degree: PhD, Functional Genomics, 2008, North Carolina State University

Subjects/Keywords: Abh; SpoVT; AbrB; transition-state regulator

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APA (6th Edition):

Sullivan, D. M. (2008). Molecular and Structural Characterization of Proteins Involved in Bacterial Adaptive Responses. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5122

Chicago Manual of Style (16th Edition):

Sullivan, Daniel Michael. “Molecular and Structural Characterization of Proteins Involved in Bacterial Adaptive Responses.” 2008. Doctoral Dissertation, North Carolina State University. Accessed October 28, 2020. http://www.lib.ncsu.edu/resolver/1840.16/5122.

MLA Handbook (7th Edition):

Sullivan, Daniel Michael. “Molecular and Structural Characterization of Proteins Involved in Bacterial Adaptive Responses.” 2008. Web. 28 Oct 2020.

Vancouver:

Sullivan DM. Molecular and Structural Characterization of Proteins Involved in Bacterial Adaptive Responses. [Internet] [Doctoral dissertation]. North Carolina State University; 2008. [cited 2020 Oct 28]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5122.

Council of Science Editors:

Sullivan DM. Molecular and Structural Characterization of Proteins Involved in Bacterial Adaptive Responses. [Doctoral Dissertation]. North Carolina State University; 2008. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5122


Montana State University

8. VanEngelen, Michael Robert. Molecular aspects of uranium toxicity : speciation and physiological targeting.

Degree: PhD, College of Engineering, 2009, Montana State University

 Uranium (U), as the uranyl ion (UO 2 ²+), is a widely distributed contaminant at several Department of Energy (DOE) sites, former war zones, and… (more)

Subjects/Keywords: Uranium.; Toxicology.; Pseudomonas.; PQQ (Biochemistry).

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APA (6th Edition):

VanEngelen, M. R. (2009). Molecular aspects of uranium toxicity : speciation and physiological targeting. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/2466

Chicago Manual of Style (16th Edition):

VanEngelen, Michael Robert. “Molecular aspects of uranium toxicity : speciation and physiological targeting.” 2009. Doctoral Dissertation, Montana State University. Accessed October 28, 2020. https://scholarworks.montana.edu/xmlui/handle/1/2466.

MLA Handbook (7th Edition):

VanEngelen, Michael Robert. “Molecular aspects of uranium toxicity : speciation and physiological targeting.” 2009. Web. 28 Oct 2020.

Vancouver:

VanEngelen MR. Molecular aspects of uranium toxicity : speciation and physiological targeting. [Internet] [Doctoral dissertation]. Montana State University; 2009. [cited 2020 Oct 28]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2466.

Council of Science Editors:

VanEngelen MR. Molecular aspects of uranium toxicity : speciation and physiological targeting. [Doctoral Dissertation]. Montana State University; 2009. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2466


University of Vienna

9. Gsöllpointner, Melanie. Untersuchungen des Einflusses einer chronischen Ethanolaufnahme auf Enzyme des Alkoholstoffwechsels im Modellorganismus.

Degree: 2018, University of Vienna

Der chronische Konsum von Alkohol führt bei mehr als 90 % der Betroffenen zu Leberschäden und stellt nach wie vor ein Problem in unserer Gesellschaft… (more)

Subjects/Keywords: 30.99 Naturwissenschaften allgemein: Sonstiges; Alkoholische Lebererkrankung / Ethanol / Lieber DeCarli Diät / Alkoholdehydrogenase / Cytochrom P450 2E1

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APA (6th Edition):

Gsöllpointner, M. (2018). Untersuchungen des Einflusses einer chronischen Ethanolaufnahme auf Enzyme des Alkoholstoffwechsels im Modellorganismus. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/52644/

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):

Gsöllpointner, Melanie. “Untersuchungen des Einflusses einer chronischen Ethanolaufnahme auf Enzyme des Alkoholstoffwechsels im Modellorganismus.” 2018. Thesis, University of Vienna. Accessed October 28, 2020. http://othes.univie.ac.at/52644/.

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

MLA Handbook (7th Edition):

Gsöllpointner, Melanie. “Untersuchungen des Einflusses einer chronischen Ethanolaufnahme auf Enzyme des Alkoholstoffwechsels im Modellorganismus.” 2018. Web. 28 Oct 2020.

Vancouver:

Gsöllpointner M. Untersuchungen des Einflusses einer chronischen Ethanolaufnahme auf Enzyme des Alkoholstoffwechsels im Modellorganismus. [Internet] [Thesis]. University of Vienna; 2018. [cited 2020 Oct 28]. Available from: http://othes.univie.ac.at/52644/.

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

Council of Science Editors:

Gsöllpointner M. Untersuchungen des Einflusses einer chronischen Ethanolaufnahme auf Enzyme des Alkoholstoffwechsels im Modellorganismus. [Thesis]. University of Vienna; 2018. Available from: http://othes.univie.ac.at/52644/

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


University of Kentucky

10. Diaz, Benjamin. STUDIES RELATING PQQ BIOSYNTHESIS TO PUTATIVE PEPTIDASES AND OPERON STRUCTURE IN PSEUDOMONAS SPECIES.

Degree: 2017, University of Kentucky

 Several bacteria isolated from the broccoli rhizosphere were assayed to compare their ability to solubilize phosphate and release pyrroloquinoline quinone (PQQ) into the surrounding media.… (more)

Subjects/Keywords: PQQ; Pseudomonas putida KT2440; Glucose Dehydrogenase; pqqF; pqqG; Environmental Microbiology and Microbial Ecology

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APA (6th Edition):

Diaz, B. (2017). STUDIES RELATING PQQ BIOSYNTHESIS TO PUTATIVE PEPTIDASES AND OPERON STRUCTURE IN PSEUDOMONAS SPECIES. (Masters Thesis). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pss_etds/95

Chicago Manual of Style (16th Edition):

Diaz, Benjamin. “STUDIES RELATING PQQ BIOSYNTHESIS TO PUTATIVE PEPTIDASES AND OPERON STRUCTURE IN PSEUDOMONAS SPECIES.” 2017. Masters Thesis, University of Kentucky. Accessed October 28, 2020. https://uknowledge.uky.edu/pss_etds/95.

MLA Handbook (7th Edition):

Diaz, Benjamin. “STUDIES RELATING PQQ BIOSYNTHESIS TO PUTATIVE PEPTIDASES AND OPERON STRUCTURE IN PSEUDOMONAS SPECIES.” 2017. Web. 28 Oct 2020.

Vancouver:

Diaz B. STUDIES RELATING PQQ BIOSYNTHESIS TO PUTATIVE PEPTIDASES AND OPERON STRUCTURE IN PSEUDOMONAS SPECIES. [Internet] [Masters thesis]. University of Kentucky; 2017. [cited 2020 Oct 28]. Available from: https://uknowledge.uky.edu/pss_etds/95.

Council of Science Editors:

Diaz B. STUDIES RELATING PQQ BIOSYNTHESIS TO PUTATIVE PEPTIDASES AND OPERON STRUCTURE IN PSEUDOMONAS SPECIES. [Masters Thesis]. University of Kentucky; 2017. Available from: https://uknowledge.uky.edu/pss_etds/95


University of Ghana

11. Owusu, E.A. Prevalence of Blood Group A2 among Group A and AB Donors Who Visit the Southern Area Blood Centre .

Degree: 2019, University of Ghana

 Introduction: The ABO blood group antigens are major antigens whose discovery paved way for the performance of safe blood transfusions and transplantations. Subgroups of the… (more)

Subjects/Keywords: Human Blood Group; Carbohydrate Blood Groups; Southern Area Blood Centre (SABC); ABH Antigens; ABO Blood Groups

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APA (6th Edition):

Owusu, E. A. (2019). Prevalence of Blood Group A2 among Group A and AB Donors Who Visit the Southern Area Blood Centre . (Masters Thesis). University of Ghana. Retrieved from http://ugspace.ug.edu.gh/handle/123456789/34352

Chicago Manual of Style (16th Edition):

Owusu, E A. “Prevalence of Blood Group A2 among Group A and AB Donors Who Visit the Southern Area Blood Centre .” 2019. Masters Thesis, University of Ghana. Accessed October 28, 2020. http://ugspace.ug.edu.gh/handle/123456789/34352.

MLA Handbook (7th Edition):

Owusu, E A. “Prevalence of Blood Group A2 among Group A and AB Donors Who Visit the Southern Area Blood Centre .” 2019. Web. 28 Oct 2020.

Vancouver:

Owusu EA. Prevalence of Blood Group A2 among Group A and AB Donors Who Visit the Southern Area Blood Centre . [Internet] [Masters thesis]. University of Ghana; 2019. [cited 2020 Oct 28]. Available from: http://ugspace.ug.edu.gh/handle/123456789/34352.

Council of Science Editors:

Owusu EA. Prevalence of Blood Group A2 among Group A and AB Donors Who Visit the Southern Area Blood Centre . [Masters Thesis]. University of Ghana; 2019. Available from: http://ugspace.ug.edu.gh/handle/123456789/34352


Rhodes University

12. Moyo, Buhle. Screening and characterization of compounds for modulators of heat shock protein (Hsp90) in a breast cancer cell model.

Degree: PhD, Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2013, Rhodes University

 Breast cancer is a leading cause of cancer death in Africa. Hsp90 has been identified as a target for anti-cancer treatments as its inhibition results… (more)

Subjects/Keywords: Heat shock proteins; Breast – Cancer; Breast – Cancer – Chemotherapy; Breast – Cancer – Treatment; Cancer cells; Naphthoquinone; PQQ (Biochemistry)

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APA (6th Edition):

Moyo, B. (2013). Screening and characterization of compounds for modulators of heat shock protein (Hsp90) in a breast cancer cell model. (Doctoral Dissertation). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1004129

Chicago Manual of Style (16th Edition):

Moyo, Buhle. “Screening and characterization of compounds for modulators of heat shock protein (Hsp90) in a breast cancer cell model.” 2013. Doctoral Dissertation, Rhodes University. Accessed October 28, 2020. http://hdl.handle.net/10962/d1004129.

MLA Handbook (7th Edition):

Moyo, Buhle. “Screening and characterization of compounds for modulators of heat shock protein (Hsp90) in a breast cancer cell model.” 2013. Web. 28 Oct 2020.

Vancouver:

Moyo B. Screening and characterization of compounds for modulators of heat shock protein (Hsp90) in a breast cancer cell model. [Internet] [Doctoral dissertation]. Rhodes University; 2013. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10962/d1004129.

Council of Science Editors:

Moyo B. Screening and characterization of compounds for modulators of heat shock protein (Hsp90) in a breast cancer cell model. [Doctoral Dissertation]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1004129


Rhodes University

13. Antunes, Edith Martins. Pyrroloiminoquinone metabolites from South African Latrunculid sponges.

Degree: Faculty of Science, Chemistry, 2003, Rhodes University

 An in depth chemical investigation of the major and minor pyrroloiminoquinone metabolites produced by four species of endemic South African Latrunculid sponges, collected from Algoa… (more)

Subjects/Keywords: Sponges  – South Africa; PQQ (Biochemistry); Marine metabolites  – South Africa

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APA (6th Edition):

Antunes, E. M. (2003). Pyrroloiminoquinone metabolites from South African Latrunculid sponges. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1005001

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):

Antunes, Edith Martins. “Pyrroloiminoquinone metabolites from South African Latrunculid sponges.” 2003. Thesis, Rhodes University. Accessed October 28, 2020. http://hdl.handle.net/10962/d1005001.

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

MLA Handbook (7th Edition):

Antunes, Edith Martins. “Pyrroloiminoquinone metabolites from South African Latrunculid sponges.” 2003. Web. 28 Oct 2020.

Vancouver:

Antunes EM. Pyrroloiminoquinone metabolites from South African Latrunculid sponges. [Internet] [Thesis]. Rhodes University; 2003. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10962/d1005001.

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

Council of Science Editors:

Antunes EM. Pyrroloiminoquinone metabolites from South African Latrunculid sponges. [Thesis]. Rhodes University; 2003. Available from: http://hdl.handle.net/10962/d1005001

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


University of Minnesota

14. Evans III, Robert. Protein structures elucidating the post-ribosomal biosynthesis of pyrroloquinoline quinone.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2017, University of Minnesota

Not applicable

Subjects/Keywords: biosynthesis; PQQ; PqqD; pyrroloquinoline quinone; RiPP; RRE

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APA (6th Edition):

Evans III, R. (2017). Protein structures elucidating the post-ribosomal biosynthesis of pyrroloquinoline quinone. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/190438

Chicago Manual of Style (16th Edition):

Evans III, Robert. “Protein structures elucidating the post-ribosomal biosynthesis of pyrroloquinoline quinone.” 2017. Doctoral Dissertation, University of Minnesota. Accessed October 28, 2020. http://hdl.handle.net/11299/190438.

MLA Handbook (7th Edition):

Evans III, Robert. “Protein structures elucidating the post-ribosomal biosynthesis of pyrroloquinoline quinone.” 2017. Web. 28 Oct 2020.

Vancouver:

Evans III R. Protein structures elucidating the post-ribosomal biosynthesis of pyrroloquinoline quinone. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/11299/190438.

Council of Science Editors:

Evans III R. Protein structures elucidating the post-ribosomal biosynthesis of pyrroloquinoline quinone. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/190438


Wake Forest University

15. Xia, Yiyuan. FUNCTIONAL EFFECT OF ALTERATIONS TO E. coli METHIONYL-tRNA SYNTHETASE BETA-LINKER LENGTH.

Degree: 2015, Wake Forest University

Aminoacyl-tRNA synthetases (AARSs) are essential enzymes that catalyze the

Subjects/Keywords: enzyme

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APA (6th Edition):

Xia, Y. (2015). FUNCTIONAL EFFECT OF ALTERATIONS TO E. coli METHIONYL-tRNA SYNTHETASE BETA-LINKER LENGTH. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/57089

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):

Xia, Yiyuan. “FUNCTIONAL EFFECT OF ALTERATIONS TO E. coli METHIONYL-tRNA SYNTHETASE BETA-LINKER LENGTH.” 2015. Thesis, Wake Forest University. Accessed October 28, 2020. http://hdl.handle.net/10339/57089.

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

MLA Handbook (7th Edition):

Xia, Yiyuan. “FUNCTIONAL EFFECT OF ALTERATIONS TO E. coli METHIONYL-tRNA SYNTHETASE BETA-LINKER LENGTH.” 2015. Web. 28 Oct 2020.

Vancouver:

Xia Y. FUNCTIONAL EFFECT OF ALTERATIONS TO E. coli METHIONYL-tRNA SYNTHETASE BETA-LINKER LENGTH. [Internet] [Thesis]. Wake Forest University; 2015. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10339/57089.

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

Council of Science Editors:

Xia Y. FUNCTIONAL EFFECT OF ALTERATIONS TO E. coli METHIONYL-tRNA SYNTHETASE BETA-LINKER LENGTH. [Thesis]. Wake Forest University; 2015. Available from: http://hdl.handle.net/10339/57089

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


North Carolina State University

16. Bobay, Benjamin Grant. Molecular and Structural Characterization of Global Transition State Regulators AbrB and Abh from Bacillus subtilis.

Degree: PhD, Biochemistry, 2005, North Carolina State University

 Bacteria remarkably and constantly adapt to their surrounding environment, especially in times of considerable environmental stress. These responses range from secretion of toxins, antibiotics and… (more)

Subjects/Keywords: Bacillus subtilis; AbrB; MS; electrospray ionization; NMR; DNA binding protein; Abh

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APA (6th Edition):

Bobay, B. G. (2005). Molecular and Structural Characterization of Global Transition State Regulators AbrB and Abh from Bacillus subtilis. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5945

Chicago Manual of Style (16th Edition):

Bobay, Benjamin Grant. “Molecular and Structural Characterization of Global Transition State Regulators AbrB and Abh from Bacillus subtilis.” 2005. Doctoral Dissertation, North Carolina State University. Accessed October 28, 2020. http://www.lib.ncsu.edu/resolver/1840.16/5945.

MLA Handbook (7th Edition):

Bobay, Benjamin Grant. “Molecular and Structural Characterization of Global Transition State Regulators AbrB and Abh from Bacillus subtilis.” 2005. Web. 28 Oct 2020.

Vancouver:

Bobay BG. Molecular and Structural Characterization of Global Transition State Regulators AbrB and Abh from Bacillus subtilis. [Internet] [Doctoral dissertation]. North Carolina State University; 2005. [cited 2020 Oct 28]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5945.

Council of Science Editors:

Bobay BG. Molecular and Structural Characterization of Global Transition State Regulators AbrB and Abh from Bacillus subtilis. [Doctoral Dissertation]. North Carolina State University; 2005. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5945

17. Neupane, Rabin. Percutaneous absorption and Skin accumulation of ABH Carbopol gel in Porcine Ear Skin.

Degree: MS, Pharmaceutical Sciences (Industrial Pharmacy), 2019, University of Toledo Health Science Campus

 Purpose A compounded Pluronic Lecithin Organogel (PLO gel) formulation of lorazepam (Ativan®), diphenhydramine hydrochloride (Benadryl®) and haloperidol (Haldol®) (ABH PLO gel) is used widely in… (more)

Subjects/Keywords: Pharmaceuticals; Transdermal system, Permeation enhancer, ABH gel, Carbopol gel

…38 7.1 ABH components… …44 9.2 Preparation of ABH Carbopol gel… …49 9.10 Percutaneous absorption of drugs from ABH Carbopol gel across porcine ear skin… …52 10.1 pH of ABH Carbopol gel formulation… …52 10.2 Viscosity of ABH Carbopol gel formulation… 

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APA (6th Edition):

Neupane, R. (2019). Percutaneous absorption and Skin accumulation of ABH Carbopol gel in Porcine Ear Skin. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1556641636092785

Chicago Manual of Style (16th Edition):

Neupane, Rabin. “Percutaneous absorption and Skin accumulation of ABH Carbopol gel in Porcine Ear Skin.” 2019. Masters Thesis, University of Toledo Health Science Campus. Accessed October 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1556641636092785.

MLA Handbook (7th Edition):

Neupane, Rabin. “Percutaneous absorption and Skin accumulation of ABH Carbopol gel in Porcine Ear Skin.” 2019. Web. 28 Oct 2020.

Vancouver:

Neupane R. Percutaneous absorption and Skin accumulation of ABH Carbopol gel in Porcine Ear Skin. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2019. [cited 2020 Oct 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1556641636092785.

Council of Science Editors:

Neupane R. Percutaneous absorption and Skin accumulation of ABH Carbopol gel in Porcine Ear Skin. [Masters Thesis]. University of Toledo Health Science Campus; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1556641636092785


Boston College

18. Harris, Katharine Morse. Studies of structure, function and mechanism in pyrimidine nucleotide biosynthesis.

Degree: PhD, Chemistry, 2012, Boston College

 Living organisms depend on enzymes for the synthesis using small molecule precursors of cellular building blocks. For example, the amino acid aspartate is synthesized in… (more)

Subjects/Keywords: catalytic regulation; enzyme catalysis; enzyme structure/function

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APA (6th Edition):

Harris, K. M. (2012). Studies of structure, function and mechanism in pyrimidine nucleotide biosynthesis. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101781

Chicago Manual of Style (16th Edition):

Harris, Katharine Morse. “Studies of structure, function and mechanism in pyrimidine nucleotide biosynthesis.” 2012. Doctoral Dissertation, Boston College. Accessed October 28, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101781.

MLA Handbook (7th Edition):

Harris, Katharine Morse. “Studies of structure, function and mechanism in pyrimidine nucleotide biosynthesis.” 2012. Web. 28 Oct 2020.

Vancouver:

Harris KM. Studies of structure, function and mechanism in pyrimidine nucleotide biosynthesis. [Internet] [Doctoral dissertation]. Boston College; 2012. [cited 2020 Oct 28]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101781.

Council of Science Editors:

Harris KM. Studies of structure, function and mechanism in pyrimidine nucleotide biosynthesis. [Doctoral Dissertation]. Boston College; 2012. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101781

19. Alfano, Marila. Etude de la biosynthèse de la monoxyde de carbone déshydrogénase, une enzyme-clé de la réaction du gaz à l'eau : Deciphering the biosynthetic pathway of carbon monoxide dehydrogenase, a key enzyme of the watergas shift reaction.

Degree: Docteur es, Chimie inorganique et bio inorganique, 2019, Université Grenoble Alpes (ComUE)

La CO déshydrogénase (CODH) est une enzyme clé de la réaction du gaz de l'eau (WGSR) chez les carboxydotrophes hydrogénogènes tels que Rhodospirillum rubrum, capable… (more)

Subjects/Keywords: Enzyme; Deshydrogenase; Monoxyde; Enzyme; Dehydrogenase; Monoxide

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APA (6th Edition):

Alfano, M. (2019). Etude de la biosynthèse de la monoxyde de carbone déshydrogénase, une enzyme-clé de la réaction du gaz à l'eau : Deciphering the biosynthetic pathway of carbon monoxide dehydrogenase, a key enzyme of the watergas shift reaction. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2019GREAV036

Chicago Manual of Style (16th Edition):

Alfano, Marila. “Etude de la biosynthèse de la monoxyde de carbone déshydrogénase, une enzyme-clé de la réaction du gaz à l'eau : Deciphering the biosynthetic pathway of carbon monoxide dehydrogenase, a key enzyme of the watergas shift reaction.” 2019. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed October 28, 2020. http://www.theses.fr/2019GREAV036.

MLA Handbook (7th Edition):

Alfano, Marila. “Etude de la biosynthèse de la monoxyde de carbone déshydrogénase, une enzyme-clé de la réaction du gaz à l'eau : Deciphering the biosynthetic pathway of carbon monoxide dehydrogenase, a key enzyme of the watergas shift reaction.” 2019. Web. 28 Oct 2020.

Vancouver:

Alfano M. Etude de la biosynthèse de la monoxyde de carbone déshydrogénase, une enzyme-clé de la réaction du gaz à l'eau : Deciphering the biosynthetic pathway of carbon monoxide dehydrogenase, a key enzyme of the watergas shift reaction. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2019. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2019GREAV036.

Council of Science Editors:

Alfano M. Etude de la biosynthèse de la monoxyde de carbone déshydrogénase, une enzyme-clé de la réaction du gaz à l'eau : Deciphering the biosynthetic pathway of carbon monoxide dehydrogenase, a key enzyme of the watergas shift reaction. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2019. Available from: http://www.theses.fr/2019GREAV036


Texas A&M University

20. Park, Jung-Woo. Cytohistological, Physiological, and Nutritional Effects of a Commercial Β-Mannanase Product in Ducklings 1-21 Days of Age.

Degree: PhD, Poultry Science, 2018, Texas A&M University

 Nutritional formula is an economical key factor to raise poultry. β-mannanase breaks the non-starch polysaccharide (NSP) backbone chains in plant-based feed, then NSP is divided… (more)

Subjects/Keywords: Duck nutrition; Enzyme

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APA (6th Edition):

Park, J. (2018). Cytohistological, Physiological, and Nutritional Effects of a Commercial Β-Mannanase Product in Ducklings 1-21 Days of Age. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173288

Chicago Manual of Style (16th Edition):

Park, Jung-Woo. “Cytohistological, Physiological, and Nutritional Effects of a Commercial Β-Mannanase Product in Ducklings 1-21 Days of Age.” 2018. Doctoral Dissertation, Texas A&M University. Accessed October 28, 2020. http://hdl.handle.net/1969.1/173288.

MLA Handbook (7th Edition):

Park, Jung-Woo. “Cytohistological, Physiological, and Nutritional Effects of a Commercial Β-Mannanase Product in Ducklings 1-21 Days of Age.” 2018. Web. 28 Oct 2020.

Vancouver:

Park J. Cytohistological, Physiological, and Nutritional Effects of a Commercial Β-Mannanase Product in Ducklings 1-21 Days of Age. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1969.1/173288.

Council of Science Editors:

Park J. Cytohistological, Physiological, and Nutritional Effects of a Commercial Β-Mannanase Product in Ducklings 1-21 Days of Age. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173288


Texas A&M University

21. Allcorn, Tucker Gregory. Evaluation of Exogenous Enzyme Combinations on Broiler Performance in Reduced Energy Diets.

Degree: MS, Poultry Science, 2016, Texas A&M University

 Two studies were performed to evaluate the efficacy of supplementing exogenous enzyme combinations on broiler growth performance in reduced nutrient density corn-soybean meal diets. In… (more)

Subjects/Keywords: Broiler; Performance; Enzyme

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APA (6th Edition):

Allcorn, T. G. (2016). Evaluation of Exogenous Enzyme Combinations on Broiler Performance in Reduced Energy Diets. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158603

Chicago Manual of Style (16th Edition):

Allcorn, Tucker Gregory. “Evaluation of Exogenous Enzyme Combinations on Broiler Performance in Reduced Energy Diets.” 2016. Masters Thesis, Texas A&M University. Accessed October 28, 2020. http://hdl.handle.net/1969.1/158603.

MLA Handbook (7th Edition):

Allcorn, Tucker Gregory. “Evaluation of Exogenous Enzyme Combinations on Broiler Performance in Reduced Energy Diets.” 2016. Web. 28 Oct 2020.

Vancouver:

Allcorn TG. Evaluation of Exogenous Enzyme Combinations on Broiler Performance in Reduced Energy Diets. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1969.1/158603.

Council of Science Editors:

Allcorn TG. Evaluation of Exogenous Enzyme Combinations on Broiler Performance in Reduced Energy Diets. [Masters Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158603

22. Beka, Robert Germain. Une alternative végétale en fromagerie : préparation d’un extrait coagulant à partir des fruits de Balanites aegyptiaca : étude biochimique et application technologique : Plant alternative for dairy : preparation of a milk-clotting extract from Balanites aegyptiaca fruits : biochimical study and technological application.

Degree: Docteur es, Ingénierie des Fonctions Biologiques, 2011, Université Lille I – Sciences et Technologies

Dans le cadre de la recherche d’un succédané à la présure, la pulpe des fruits de B. aegyptiaca a été utilisée comme source d’enzyme coagulant.… (more)

Subjects/Keywords: Enzyme coagulant; 660.634

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APA (6th Edition):

Beka, R. G. (2011). Une alternative végétale en fromagerie : préparation d’un extrait coagulant à partir des fruits de Balanites aegyptiaca : étude biochimique et application technologique : Plant alternative for dairy : preparation of a milk-clotting extract from Balanites aegyptiaca fruits : biochimical study and technological application. (Doctoral Dissertation). Université Lille I – Sciences et Technologies. Retrieved from http://www.theses.fr/2011LIL10124

Chicago Manual of Style (16th Edition):

Beka, Robert Germain. “Une alternative végétale en fromagerie : préparation d’un extrait coagulant à partir des fruits de Balanites aegyptiaca : étude biochimique et application technologique : Plant alternative for dairy : preparation of a milk-clotting extract from Balanites aegyptiaca fruits : biochimical study and technological application.” 2011. Doctoral Dissertation, Université Lille I – Sciences et Technologies. Accessed October 28, 2020. http://www.theses.fr/2011LIL10124.

MLA Handbook (7th Edition):

Beka, Robert Germain. “Une alternative végétale en fromagerie : préparation d’un extrait coagulant à partir des fruits de Balanites aegyptiaca : étude biochimique et application technologique : Plant alternative for dairy : preparation of a milk-clotting extract from Balanites aegyptiaca fruits : biochimical study and technological application.” 2011. Web. 28 Oct 2020.

Vancouver:

Beka RG. Une alternative végétale en fromagerie : préparation d’un extrait coagulant à partir des fruits de Balanites aegyptiaca : étude biochimique et application technologique : Plant alternative for dairy : preparation of a milk-clotting extract from Balanites aegyptiaca fruits : biochimical study and technological application. [Internet] [Doctoral dissertation]. Université Lille I – Sciences et Technologies; 2011. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2011LIL10124.

Council of Science Editors:

Beka RG. Une alternative végétale en fromagerie : préparation d’un extrait coagulant à partir des fruits de Balanites aegyptiaca : étude biochimique et application technologique : Plant alternative for dairy : preparation of a milk-clotting extract from Balanites aegyptiaca fruits : biochimical study and technological application. [Doctoral Dissertation]. Université Lille I – Sciences et Technologies; 2011. Available from: http://www.theses.fr/2011LIL10124


University of Manitoba

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

Degree: Chemistry, 2016, University of Manitoba

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

Subjects/Keywords: Biochemistry; Enzyme dynamics

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Hutchings, Roy. “Probing the conformational dynamics of an OTU deubiquitinase enzyme active site.” 2016. Masters Thesis, University of Manitoba. Accessed October 28, 2020. http://hdl.handle.net/1993/31784.

MLA Handbook (7th Edition):

Hutchings, Roy. “Probing the conformational dynamics of an OTU deubiquitinase enzyme active site.” 2016. Web. 28 Oct 2020.

Vancouver:

Hutchings R. Probing the conformational dynamics of an OTU deubiquitinase enzyme active site. [Internet] [Masters thesis]. University of Manitoba; 2016. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1993/31784.

Council of Science Editors:

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


University of Notre Dame

24. Beatrice Blanc. Relationship between active site structure and chemistry in dioxygen producing chlorite dismutases</h1>.

Degree: Chemistry and Biochemistry, 2012, University of Notre Dame

  This thesis focuses on understanding the relationship between the active site structure and function in the heme-containing enzyme chlorite dismutase from Dechloromonas aromatica (DaCld).… (more)

Subjects/Keywords: Heme enzyme; Oxygen

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APA (6th Edition):

Blanc, B. (2012). Relationship between active site structure and chemistry in dioxygen producing chlorite dismutases</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/3j333199s86

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):

Blanc, Beatrice. “Relationship between active site structure and chemistry in dioxygen producing chlorite dismutases</h1>.” 2012. Thesis, University of Notre Dame. Accessed October 28, 2020. https://curate.nd.edu/show/3j333199s86.

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

MLA Handbook (7th Edition):

Blanc, Beatrice. “Relationship between active site structure and chemistry in dioxygen producing chlorite dismutases</h1>.” 2012. Web. 28 Oct 2020.

Vancouver:

Blanc B. Relationship between active site structure and chemistry in dioxygen producing chlorite dismutases</h1>. [Internet] [Thesis]. University of Notre Dame; 2012. [cited 2020 Oct 28]. Available from: https://curate.nd.edu/show/3j333199s86.

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

Council of Science Editors:

Blanc B. Relationship between active site structure and chemistry in dioxygen producing chlorite dismutases</h1>. [Thesis]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/3j333199s86

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


University of Illinois – Urbana-Champaign

25. Tang, Weixin. Mechanistic studies of lanthipeptide biosynthesis.

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

 Natural products and natural product derivatives have been the leading source of pharmaceutical compounds since the initial application of modern medicine. To fight the increasing… (more)

Subjects/Keywords: Enzyme mechanism; Lanthipeptide

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APA (6th Edition):

Tang, W. (2015). Mechanistic studies of lanthipeptide biosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78752

Chicago Manual of Style (16th Edition):

Tang, Weixin. “Mechanistic studies of lanthipeptide biosynthesis.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 28, 2020. http://hdl.handle.net/2142/78752.

MLA Handbook (7th Edition):

Tang, Weixin. “Mechanistic studies of lanthipeptide biosynthesis.” 2015. Web. 28 Oct 2020.

Vancouver:

Tang W. Mechanistic studies of lanthipeptide biosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2142/78752.

Council of Science Editors:

Tang W. Mechanistic studies of lanthipeptide biosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78752


University of Minnesota

26. Hanson, Benjamin. Isolating and Assaying Unspecific Peroxygenase and Flavin Binding Enzymes for in vitro Terpenoid Biosynthesis.

Degree: MS, Biochemistry, Molecular Bio, and Biophysics, 2018, University of Minnesota

 Terpenoids are an exceptionally large family of natural products, and contain numerous bioactive members that are pharmaceutically important. While most research into terpenoids and their… (more)

Subjects/Keywords: biocatalysis; enzyme; Terpenoid

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APA (6th Edition):

Hanson, B. (2018). Isolating and Assaying Unspecific Peroxygenase and Flavin Binding Enzymes for in vitro Terpenoid Biosynthesis. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/198972

Chicago Manual of Style (16th Edition):

Hanson, Benjamin. “Isolating and Assaying Unspecific Peroxygenase and Flavin Binding Enzymes for in vitro Terpenoid Biosynthesis.” 2018. Masters Thesis, University of Minnesota. Accessed October 28, 2020. http://hdl.handle.net/11299/198972.

MLA Handbook (7th Edition):

Hanson, Benjamin. “Isolating and Assaying Unspecific Peroxygenase and Flavin Binding Enzymes for in vitro Terpenoid Biosynthesis.” 2018. Web. 28 Oct 2020.

Vancouver:

Hanson B. Isolating and Assaying Unspecific Peroxygenase and Flavin Binding Enzymes for in vitro Terpenoid Biosynthesis. [Internet] [Masters thesis]. University of Minnesota; 2018. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/11299/198972.

Council of Science Editors:

Hanson B. Isolating and Assaying Unspecific Peroxygenase and Flavin Binding Enzymes for in vitro Terpenoid Biosynthesis. [Masters Thesis]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/198972


University of New South Wales

27. Prabhu, Anika. The regulation of DHCR7 - a key enzyme in cholesterol synthesis.

Degree: Biotechnology & Biomolecular Sciences, 2016, University of New South Wales

 Cholesterol is a vital lipid for mammalian life. It is essential for the structure of cell membranes, fetal development, and as a precursor for steroid… (more)

Subjects/Keywords: Cholesterol; DHCR7; Enzyme

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APA (6th Edition):

Prabhu, A. (2016). The regulation of DHCR7 - a key enzyme in cholesterol synthesis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57100 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42487/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Prabhu, Anika. “The regulation of DHCR7 - a key enzyme in cholesterol synthesis.” 2016. Doctoral Dissertation, University of New South Wales. Accessed October 28, 2020. http://handle.unsw.edu.au/1959.4/57100 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42487/SOURCE02?view=true.

MLA Handbook (7th Edition):

Prabhu, Anika. “The regulation of DHCR7 - a key enzyme in cholesterol synthesis.” 2016. Web. 28 Oct 2020.

Vancouver:

Prabhu A. The regulation of DHCR7 - a key enzyme in cholesterol synthesis. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2020 Oct 28]. Available from: http://handle.unsw.edu.au/1959.4/57100 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42487/SOURCE02?view=true.

Council of Science Editors:

Prabhu A. The regulation of DHCR7 - a key enzyme in cholesterol synthesis. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/57100 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42487/SOURCE02?view=true


University of Otago

28. Siakkou, Eleni. Kinetics of Cysteine Dioxygenase .

Degree: 2011, University of Otago

 Cysteine dioxygenase (CDO) is a non-heme mono-iron enzyme, which catalyses the first step of cysteine metabolism in various species. It is known that malfunction of… (more)

Subjects/Keywords: cysteine dioxygenase; enzyme activity assay; enzyme kinetics; non-heme iron enzyme

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

APA (6th Edition):

Siakkou, E. (2011). Kinetics of Cysteine Dioxygenase . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/1932

Chicago Manual of Style (16th Edition):

Siakkou, Eleni. “Kinetics of Cysteine Dioxygenase .” 2011. Doctoral Dissertation, University of Otago. Accessed October 28, 2020. http://hdl.handle.net/10523/1932.

MLA Handbook (7th Edition):

Siakkou, Eleni. “Kinetics of Cysteine Dioxygenase .” 2011. Web. 28 Oct 2020.

Vancouver:

Siakkou E. Kinetics of Cysteine Dioxygenase . [Internet] [Doctoral dissertation]. University of Otago; 2011. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10523/1932.

Council of Science Editors:

Siakkou E. Kinetics of Cysteine Dioxygenase . [Doctoral Dissertation]. University of Otago; 2011. Available from: http://hdl.handle.net/10523/1932


Rhodes University

29. Walmsley, Tara Aisling. An investigation into the bacterial diversity associated with South African latrunculid sponges that produce bioactive secondary metabolites.

Degree: PhD, Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2014, Rhodes University

 Algoa Bay Latrunculid sponges are well known for their production of cytotoxic pyrroloiminoquinones with speculation that these secondary metabolites may have a microbial origin. This… (more)

Subjects/Keywords: Sponges  – South Africa  – Algoa Bay; Sponges  – Classification; Metabolites  – South Africa  – Algoa Bay; Marine metabolites  – South Africa  – Algoa Bay; PQQ (Biochemistry); Bacterial diversity

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

APA (6th Edition):

Walmsley, T. A. (2014). An investigation into the bacterial diversity associated with South African latrunculid sponges that produce bioactive secondary metabolites. (Doctoral Dissertation). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1012943

Chicago Manual of Style (16th Edition):

Walmsley, Tara Aisling. “An investigation into the bacterial diversity associated with South African latrunculid sponges that produce bioactive secondary metabolites.” 2014. Doctoral Dissertation, Rhodes University. Accessed October 28, 2020. http://hdl.handle.net/10962/d1012943.

MLA Handbook (7th Edition):

Walmsley, Tara Aisling. “An investigation into the bacterial diversity associated with South African latrunculid sponges that produce bioactive secondary metabolites.” 2014. Web. 28 Oct 2020.

Vancouver:

Walmsley TA. An investigation into the bacterial diversity associated with South African latrunculid sponges that produce bioactive secondary metabolites. [Internet] [Doctoral dissertation]. Rhodes University; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10962/d1012943.

Council of Science Editors:

Walmsley TA. An investigation into the bacterial diversity associated with South African latrunculid sponges that produce bioactive secondary metabolites. [Doctoral Dissertation]. Rhodes University; 2014. Available from: http://hdl.handle.net/10962/d1012943

30. Κρεμμύδας, Γεράσιμος. Προσδιορισμός μηχανισμού καταστολής φυτοπαθογόνων μυκήτων από το pseudomonas fluorescens Χ και ανάπτυξη μολυσμάτων βακτηρίων στο κάλυμμα σπόρων ζαχαροτεύτλου.

Degree: 2011, Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών

Pseudomonas fluorescens X has the ability to suppress seed and seedling damping-offin sugar beet and cucumber. Spontaneous mutagenesis and screening a library of 12000mutants, plasmid… (more)

Subjects/Keywords: Πυρρολοκινολινκινόνη; Αφυδρογονάση της γλυκόζης; Μη ριβοσωμικές πεπτιδικές συνθετάσες; Μεταγραφικοί παράγοντες; PQQ; Gcd; NRPS; Transcriptional regulator; Pyrroloquinoline quinone; Glucose dehydrogenase; Non ribosomal peptide synthetase

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

APA (6th Edition):

Κρεμμύδας, . . (2011). Προσδιορισμός μηχανισμού καταστολής φυτοπαθογόνων μυκήτων από το pseudomonas fluorescens Χ και ανάπτυξη μολυσμάτων βακτηρίων στο κάλυμμα σπόρων ζαχαροτεύτλου. (Thesis). Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών. Retrieved from http://hdl.handle.net/10442/hedi/27099

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):

Κρεμμύδας, Γεράσιμος. “Προσδιορισμός μηχανισμού καταστολής φυτοπαθογόνων μυκήτων από το pseudomonas fluorescens Χ και ανάπτυξη μολυσμάτων βακτηρίων στο κάλυμμα σπόρων ζαχαροτεύτλου.” 2011. Thesis, Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών. Accessed October 28, 2020. http://hdl.handle.net/10442/hedi/27099.

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

MLA Handbook (7th Edition):

Κρεμμύδας, Γεράσιμος. “Προσδιορισμός μηχανισμού καταστολής φυτοπαθογόνων μυκήτων από το pseudomonas fluorescens Χ και ανάπτυξη μολυσμάτων βακτηρίων στο κάλυμμα σπόρων ζαχαροτεύτλου.” 2011. Web. 28 Oct 2020.

Vancouver:

Κρεμμύδας . Προσδιορισμός μηχανισμού καταστολής φυτοπαθογόνων μυκήτων από το pseudomonas fluorescens Χ και ανάπτυξη μολυσμάτων βακτηρίων στο κάλυμμα σπόρων ζαχαροτεύτλου. [Internet] [Thesis]. Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών; 2011. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10442/hedi/27099.

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

Council of Science Editors:

Κρεμμύδας . Προσδιορισμός μηχανισμού καταστολής φυτοπαθογόνων μυκήτων από το pseudomonas fluorescens Χ και ανάπτυξη μολυσμάτων βακτηρίων στο κάλυμμα σπόρων ζαχαροτεύτλου. [Thesis]. Agricultural University of Athens; Γεωπονικό Πανεπιστήμιο Αθηνών; 2011. Available from: http://hdl.handle.net/10442/hedi/27099

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

[1] [2] [3] [4] [5] … [107]

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