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You searched for +publisher:"University of Texas – Austin" +contributor:("Alper, Hal S"). Showing records 1 – 10 of 10 total matches.

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University of Texas – Austin

1. Blazeck, John James. Harnessing Yarrowia lipolytica’s potential as a lipid and alkane production platform.

Degree: PhD, Chemical Engineering, 2013, University of Texas – Austin

 Engineering cellular phenotype can enable the in vivo synthesis of renewable fuels, industrial precursors, and pharmaceuticals. Achieving economic viability requires the use of a cellular… (more)

Subjects/Keywords: Yarrowia lipolytica; Metabolic engineering; Pentane; Itaconic acid; Lipid; Biodiesel; Promoter engineering; Hybrid promoter engineering; Gene expression

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

APA (6th Edition):

Blazeck, J. J. (2013). Harnessing Yarrowia lipolytica’s potential as a lipid and alkane production platform. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/44060

Chicago Manual of Style (16th Edition):

Blazeck, John James. “Harnessing Yarrowia lipolytica’s potential as a lipid and alkane production platform.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/44060.

MLA Handbook (7th Edition):

Blazeck, John James. “Harnessing Yarrowia lipolytica’s potential as a lipid and alkane production platform.” 2013. Web. 18 Oct 2019.

Vancouver:

Blazeck JJ. Harnessing Yarrowia lipolytica’s potential as a lipid and alkane production platform. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/44060.

Council of Science Editors:

Blazeck JJ. Harnessing Yarrowia lipolytica’s potential as a lipid and alkane production platform. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/44060


University of Texas – Austin

2. Abatemarco, Joseph T. Novel approaches for the evolutionary engineering of pathways in saccharomyces cerevisiae.

Degree: PhD, Chemical Engineering, 2017, University of Texas – Austin

 Modern biotechnological tools are making microbial production of chemicals, fuels, and pharmaceuticals increasingly practical and economically feasible. The field of metabolic engineering aims to enable… (more)

Subjects/Keywords: Metabolic engineering; Directed evolution

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APA (6th Edition):

Abatemarco, J. T. (2017). Novel approaches for the evolutionary engineering of pathways in saccharomyces cerevisiae. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72770

Chicago Manual of Style (16th Edition):

Abatemarco, Joseph T. “Novel approaches for the evolutionary engineering of pathways in saccharomyces cerevisiae.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/72770.

MLA Handbook (7th Edition):

Abatemarco, Joseph T. “Novel approaches for the evolutionary engineering of pathways in saccharomyces cerevisiae.” 2017. Web. 18 Oct 2019.

Vancouver:

Abatemarco JT. Novel approaches for the evolutionary engineering of pathways in saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/72770.

Council of Science Editors:

Abatemarco JT. Novel approaches for the evolutionary engineering of pathways in saccharomyces cerevisiae. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/72770


University of Texas – Austin

3. Lanza, Amanda Morgan. Novel tools for engineering eukaryotic cells using a systems level approach.

Degree: PhD, Chemical Engineering, 2013, University of Texas – Austin

 Engineered cellular systems are a promising avenue for production of a wide range of useful products including renewable fuels, commodity and specialty chemicals, industrial enzymes,… (more)

Subjects/Keywords: Eukaryotes; HT1080; GCN5; Codon optimization; Selection markers; Zeocin; Cre recombinase; Biotechnology; Tool development

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APA (6th Edition):

Lanza, A. M. (2013). Novel tools for engineering eukaryotic cells using a systems level approach. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30449

Chicago Manual of Style (16th Edition):

Lanza, Amanda Morgan. “Novel tools for engineering eukaryotic cells using a systems level approach.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/30449.

MLA Handbook (7th Edition):

Lanza, Amanda Morgan. “Novel tools for engineering eukaryotic cells using a systems level approach.” 2013. Web. 18 Oct 2019.

Vancouver:

Lanza AM. Novel tools for engineering eukaryotic cells using a systems level approach. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/30449.

Council of Science Editors:

Lanza AM. Novel tools for engineering eukaryotic cells using a systems level approach. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/30449


University of Texas – Austin

4. -7973-9371. Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses.

Degree: PhD, Cell and Molecular Biology, 2019, University of Texas – Austin

 Yeast has long been the sine qua non of model organisms due to its experimental tractability. Recent advances in biology, such as CRISPR/Cas9 editing, promise… (more)

Subjects/Keywords: Biotechnology; Evolution

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APA (6th Edition):

-7973-9371. (2019). Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2162

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

Chicago Manual of Style (16th Edition):

-7973-9371. “Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://dx.doi.org/10.26153/tsw/2162.

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

MLA Handbook (7th Edition):

-7973-9371. “Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses.” 2019. Web. 18 Oct 2019.

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

Vancouver:

-7973-9371. Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2019 Oct 18]. Available from: http://dx.doi.org/10.26153/tsw/2162.

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

Council of Science Editors:

-7973-9371. Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2162

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


University of Texas – Austin

5. Wang, Bo, Ph. D. in chemical engineering. High-throughput analysis of native antibody repertoires for therapeutics discovery.

Degree: PhD, Chemical Engineering, 2016, University of Texas – Austin

 Adaptive immunity is the foundation of recognition and protection against a diverse array of pathogens. The humoral arm of adaptive immunity whose most significant effector… (more)

Subjects/Keywords: Native antibody repertoire; Discovery; Analysis; High-throughput

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APA (6th Edition):

Wang, Bo, P. D. i. c. e. (2016). High-throughput analysis of native antibody repertoires for therapeutics discovery. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72724

Chicago Manual of Style (16th Edition):

Wang, Bo, Ph D in chemical engineering. “High-throughput analysis of native antibody repertoires for therapeutics discovery.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/72724.

MLA Handbook (7th Edition):

Wang, Bo, Ph D in chemical engineering. “High-throughput analysis of native antibody repertoires for therapeutics discovery.” 2016. Web. 18 Oct 2019.

Vancouver:

Wang, Bo PDice. High-throughput analysis of native antibody repertoires for therapeutics discovery. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/72724.

Council of Science Editors:

Wang, Bo PDice. High-throughput analysis of native antibody repertoires for therapeutics discovery. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/72724


University of Texas – Austin

6. Paley, Olga M. Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic.

Degree: PhD, Chemical Engineering, 2014, University of Texas – Austin

 Many cancers have long been known to display an absolute requirement for the amino acid methionine (L-Met). Studies have shown that in the absence of… (more)

Subjects/Keywords: Protein engineering; Enzyme engineering; Cancer; Melanoma; Neuroblastoma; Prostate carcinoma; Genetic selection; Protein therapeutic

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APA (6th Edition):

Paley, O. M. (2014). Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31302

Chicago Manual of Style (16th Edition):

Paley, Olga M. “Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/31302.

MLA Handbook (7th Edition):

Paley, Olga M. “Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic.” 2014. Web. 18 Oct 2019.

Vancouver:

Paley OM. Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/31302.

Council of Science Editors:

Paley OM. Engineering a novel human methionine degrading enzyme as a broadly effective cancer therapeutic. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31302

7. Lee, Sun-Mi. Combinatorial engineering of Saccharomyces cerevisiae for efficient pentose catabolism.

Degree: PhD, Chemical Engineering, 2014, University of Texas – Austin

 The efficient fermentation of lignocellulosic biomass would enable more economically and environmentally friendly production of biofuels and biochemicals. Yet, Saccharomyces cerevisiae, a platform organism for… (more)

Subjects/Keywords: Pentose; Saccharomyces cerevisiae

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APA (6th Edition):

Lee, S. (2014). Combinatorial engineering of Saccharomyces cerevisiae for efficient pentose catabolism. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31297

Chicago Manual of Style (16th Edition):

Lee, Sun-Mi. “Combinatorial engineering of Saccharomyces cerevisiae for efficient pentose catabolism.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/31297.

MLA Handbook (7th Edition):

Lee, Sun-Mi. “Combinatorial engineering of Saccharomyces cerevisiae for efficient pentose catabolism.” 2014. Web. 18 Oct 2019.

Vancouver:

Lee S. Combinatorial engineering of Saccharomyces cerevisiae for efficient pentose catabolism. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/31297.

Council of Science Editors:

Lee S. Combinatorial engineering of Saccharomyces cerevisiae for efficient pentose catabolism. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31297


University of Texas – Austin

8. Crook, Nathan Charles. Novel approaches for metabolic engineering of yeast at multiple scales.

Degree: PhD, Chemical Engineering, 2014, University of Texas – Austin

 Living systems contain enormous potential to solve many pressing engineering problems, including the production of usable energy, the synthesis and degradation of a variety of… (more)

Subjects/Keywords: Metabolic engineering; Yeast

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APA (6th Edition):

Crook, N. C. (2014). Novel approaches for metabolic engineering of yeast at multiple scales. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/44083

Chicago Manual of Style (16th Edition):

Crook, Nathan Charles. “Novel approaches for metabolic engineering of yeast at multiple scales.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/44083.

MLA Handbook (7th Edition):

Crook, Nathan Charles. “Novel approaches for metabolic engineering of yeast at multiple scales.” 2014. Web. 18 Oct 2019.

Vancouver:

Crook NC. Novel approaches for metabolic engineering of yeast at multiple scales. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/44083.

Council of Science Editors:

Crook NC. Novel approaches for metabolic engineering of yeast at multiple scales. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/44083

9. Knight, Rebecca Anne. Coordinated response and regulation of carotenogenesis in Thermosynechococcus elongatus (BP-1) : implications for commercial application.

Degree: PhD, Plant Biology, 2014, University of Texas – Austin

 If small isoprenoids, the starting component of carotenoids, can be efficiently excreted from thermophilic cyanobacteria, they could help satisfy the demand for sustainably produced hydrocarbons.… (more)

Subjects/Keywords: Thermophile; Cyanobacteria; Isoprenoids; Metabolic engineering; Light wavelength; LED; Photobioreactor; RNASeq; WGCNA; Subtractive genomics; Targeted mutagenesis

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APA (6th Edition):

Knight, R. A. (2014). Coordinated response and regulation of carotenogenesis in Thermosynechococcus elongatus (BP-1) : implications for commercial application. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28483

Chicago Manual of Style (16th Edition):

Knight, Rebecca Anne. “Coordinated response and regulation of carotenogenesis in Thermosynechococcus elongatus (BP-1) : implications for commercial application.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/28483.

MLA Handbook (7th Edition):

Knight, Rebecca Anne. “Coordinated response and regulation of carotenogenesis in Thermosynechococcus elongatus (BP-1) : implications for commercial application.” 2014. Web. 18 Oct 2019.

Vancouver:

Knight RA. Coordinated response and regulation of carotenogenesis in Thermosynechococcus elongatus (BP-1) : implications for commercial application. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/28483.

Council of Science Editors:

Knight RA. Coordinated response and regulation of carotenogenesis in Thermosynechococcus elongatus (BP-1) : implications for commercial application. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/28483

10. Chrysostomou, Constantine. Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires.

Degree: PhD, Chemical Engineering, 2014, University of Texas – Austin

 Antibodies are essential molecules that help to provide immunity against a vast population of environmental pathogens. This antibody conferred protection is dependent upon genetic diversification… (more)

Subjects/Keywords: Next generation sequencing; Immunology; Repertoires; Statistical analyses; Germline alignment; Repertoire analysis

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APA (6th Edition):

Chrysostomou, C. (2014). Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30450

Chicago Manual of Style (16th Edition):

Chrysostomou, Constantine. “Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed October 18, 2019. http://hdl.handle.net/2152/30450.

MLA Handbook (7th Edition):

Chrysostomou, Constantine. “Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires.” 2014. Web. 18 Oct 2019.

Vancouver:

Chrysostomou C. Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152/30450.

Council of Science Editors:

Chrysostomou C. Addressing intrinsic challenges for next generation sequencing of immunoglobulin repertoires. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/30450

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