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You searched for +publisher:"University of Texas – Austin" +contributor:("Georgiou, George"). Showing records 1 – 30 of 84 total matches.

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University of Texas – Austin

1. Hoi, Kam Hon. Global survey of the immunoglobulin repertoire using next generation sequencing technology.

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

 Specific and sensitive recognition of foreign agents is a critical attribute of the overall effective immune system required for maintaining host protection against challenge from… (more)

Subjects/Keywords: B cell receptor; Antibody repertoire; Next generation sequencing; Bioinformatics

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APA (6th Edition):

Hoi, K. H. (2014). Global survey of the immunoglobulin repertoire using next generation sequencing technology. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/28322

Chicago Manual of Style (16th Edition):

Hoi, Kam Hon. “Global survey of the immunoglobulin repertoire using next generation sequencing technology.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/28322.

MLA Handbook (7th Edition):

Hoi, Kam Hon. “Global survey of the immunoglobulin repertoire using next generation sequencing technology.” 2014. Web. 27 Nov 2020.

Vancouver:

Hoi KH. Global survey of the immunoglobulin repertoire using next generation sequencing technology. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/28322.

Council of Science Editors:

Hoi KH. Global survey of the immunoglobulin repertoire using next generation sequencing technology. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/28322


University of Texas – Austin

2. King, Gregory Ryan. Comparative systemic analysis of human immunoglobulin repertoires.

Degree: MA, Microbiology, 2019, University of Texas – Austin

 The humoral immune system is majorly composed of B cells producing effector immunoglobulin molecules, the vast diversity of which allow for the neutralization of pathogenic… (more)

Subjects/Keywords: Microbiology; Immunology; Bioinformatics; Antibody repertoire; Human immunoglobulin repertoires; B cells; Humoral immune system; Immunoglobulin molecules

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APA (6th Edition):

King, G. R. (2019). Comparative systemic analysis of human immunoglobulin repertoires. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72720

Chicago Manual of Style (16th Edition):

King, Gregory Ryan. “Comparative systemic analysis of human immunoglobulin repertoires.” 2019. Masters Thesis, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/72720.

MLA Handbook (7th Edition):

King, Gregory Ryan. “Comparative systemic analysis of human immunoglobulin repertoires.” 2019. Web. 27 Nov 2020.

Vancouver:

King GR. Comparative systemic analysis of human immunoglobulin repertoires. [Internet] [Masters thesis]. University of Texas – Austin; 2019. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/72720.

Council of Science Editors:

King GR. Comparative systemic analysis of human immunoglobulin repertoires. [Masters Thesis]. University of Texas – Austin; 2019. Available from: http://hdl.handle.net/2152/72720


University of Texas – Austin

3. -5387-6362. The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase.

Degree: PhD, Biochemistry, 2018, University of Texas – Austin

 Peroxy-containing compounds represent a large class of natural products with many demonstrated beneficial effects to human health. Yet, very little is known about how endoperoxide… (more)

Subjects/Keywords: Endoperoxide formation; Tyrosyl radical; Non-heme iron protein; Novel α-ketoglutarate binding orientation; CGS-like protein; Engineered enzyme; Salt dependence; Substrate selectivity shift

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APA (6th Edition):

-5387-6362. (2018). The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68396

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-5387-6362. “The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/68396.

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

MLA Handbook (7th Edition):

-5387-6362. “The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase.” 2018. Web. 27 Nov 2020.

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

Vancouver:

-5387-6362. The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/68396.

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

Council of Science Editors:

-5387-6362. The mechanism study of fumitremorgin B dioxygenase and engineered human cystathionine gamma lyase. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68396

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


University of Texas – Austin

4. -7757-895X. Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis.

Degree: PhD, Biomedical Engineering, 2020, University of Texas – Austin

 Multiple sclerosis (MS) is a debilitating neurodegenerative autoimmune disorder caused by autoreactive T cells that recognize and initiate immune attack of the myelin sheath that… (more)

Subjects/Keywords: T cell receptor; TCR; Multiple sclerosis; MS; Protein engineering; T cell engineering; T regulatory cells; Cellular therapeutics; Autoimmunity; Yeast display; T cell activation

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APA (6th Edition):

-7757-895X. (2020). Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9439

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

Chicago Manual of Style (16th Edition):

-7757-895X. “Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://dx.doi.org/10.26153/tsw/9439.

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

MLA Handbook (7th Edition):

-7757-895X. “Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis.” 2020. Web. 27 Nov 2020.

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

Vancouver:

-7757-895X. Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Nov 27]. Available from: http://dx.doi.org/10.26153/tsw/9439.

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

Council of Science Editors:

-7757-895X. Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/9439

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


University of Texas – Austin

5. Horton, Andrew Pitchford. Methods for proteomic characterization of antibody repertoires and de novo peptide sequencing.

Degree: PhD, Biomedical engineering, 2016, University of Texas – Austin

 Driven by the increased performance and availability of protein mass spectrometry and next generation sequencing technologies, research in proteomics and systems biology has expanded far… (more)

Subjects/Keywords: Mass spectrometry; De novo peptide sequencing; Immunology; Antibody repertoire

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APA (6th Edition):

Horton, A. P. (2016). Methods for proteomic characterization of antibody repertoires and de novo peptide sequencing. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/39578

Chicago Manual of Style (16th Edition):

Horton, Andrew Pitchford. “Methods for proteomic characterization of antibody repertoires and de novo peptide sequencing.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/39578.

MLA Handbook (7th Edition):

Horton, Andrew Pitchford. “Methods for proteomic characterization of antibody repertoires and de novo peptide sequencing.” 2016. Web. 27 Nov 2020.

Vancouver:

Horton AP. Methods for proteomic characterization of antibody repertoires and de novo peptide sequencing. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/39578.

Council of Science Editors:

Horton AP. Methods for proteomic characterization of antibody repertoires and de novo peptide sequencing. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/39578

6. -9568-158X. Elucidation of the human B cell immune repertoire by high-throughput sequencing and computational simulation.

Degree: PhD, Cell and molecular biology, 2016, University of Texas – Austin

 The human immune system carefully balances the need to maintain stable responses to familiar stimuli with the need for agile responses to an ever changing… (more)

Subjects/Keywords: Systems immunology; Systems biology; Immunology; Antibody repertoire

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APA (6th Edition):

-9568-158X. (2016). Elucidation of the human B cell immune repertoire by high-throughput sequencing and computational simulation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/45679

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

Chicago Manual of Style (16th Edition):

-9568-158X. “Elucidation of the human B cell immune repertoire by high-throughput sequencing and computational simulation.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/45679.

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

MLA Handbook (7th Edition):

-9568-158X. “Elucidation of the human B cell immune repertoire by high-throughput sequencing and computational simulation.” 2016. Web. 27 Nov 2020.

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

Vancouver:

-9568-158X. Elucidation of the human B cell immune repertoire by high-throughput sequencing and computational simulation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/45679.

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

Council of Science Editors:

-9568-158X. Elucidation of the human B cell immune repertoire by high-throughput sequencing and computational simulation. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/45679

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


University of Texas – Austin

7. Kang, Tae Hyun, 1977-. Fc engineering for the reprogramming the effector functions of antibodies for improved therapeutic potency.

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

 Monoclonal antibodies (mAb) are very important for cancer therapy, as they target cancerous cells without side effects. mAbsrecognize cell-surface proteins on cancerous cells and mediate… (more)

Subjects/Keywords: Fc engineering; FcγR; ADCC

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APA (6th Edition):

Kang, Tae Hyun, 1. (2014). Fc engineering for the reprogramming the effector functions of antibodies for improved therapeutic potency. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63848

Chicago Manual of Style (16th Edition):

Kang, Tae Hyun, 1977-. “Fc engineering for the reprogramming the effector functions of antibodies for improved therapeutic potency.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/63848.

MLA Handbook (7th Edition):

Kang, Tae Hyun, 1977-. “Fc engineering for the reprogramming the effector functions of antibodies for improved therapeutic potency.” 2014. Web. 27 Nov 2020.

Vancouver:

Kang, Tae Hyun 1. Fc engineering for the reprogramming the effector functions of antibodies for improved therapeutic potency. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/63848.

Council of Science Editors:

Kang, Tae Hyun 1. Fc engineering for the reprogramming the effector functions of antibodies for improved therapeutic potency. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/63848


University of Texas – Austin

8. Quandt, Erik Michael. Genetic and biochemical dissection of complex evolved traits in bacteria.

Degree: PhD, Cell and Molecular Biology, 2014, University of Texas – Austin

 Evolutionary innovations often arise from complex genetic and ecological interactions, which can make it challenging to understand retrospectively how a novel trait arose. In a… (more)

Subjects/Keywords: REGRES; Complex genetic traits; Long-term evolution experiment; Escherichia coli; Aerobic citrate utilization; Cit+; Evolution; Caffeine; Synthetic biology

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APA (6th Edition):

Quandt, E. M. (2014). Genetic and biochemical dissection of complex evolved traits in bacteria. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31294

Chicago Manual of Style (16th Edition):

Quandt, Erik Michael. “Genetic and biochemical dissection of complex evolved traits in bacteria.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/31294.

MLA Handbook (7th Edition):

Quandt, Erik Michael. “Genetic and biochemical dissection of complex evolved traits in bacteria.” 2014. Web. 27 Nov 2020.

Vancouver:

Quandt EM. Genetic and biochemical dissection of complex evolved traits in bacteria. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/31294.

Council of Science Editors:

Quandt EM. Genetic and biochemical dissection of complex evolved traits in bacteria. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31294

9. -3503-5102. Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus.

Degree: PhD, Cell and molecular biology, 2016, University of Texas – Austin

 All biological life lives under the constant threat of viral infection. From the earliest homo sapiens until now well into the 21st century, the destruction… (more)

Subjects/Keywords: Virus; Antibody

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APA (6th Edition):

-3503-5102. (2016). Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46638

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

Chicago Manual of Style (16th Edition):

-3503-5102. “Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/46638.

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

MLA Handbook (7th Edition):

-3503-5102. “Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus.” 2016. Web. 27 Nov 2020.

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

Vancouver:

-3503-5102. Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/46638.

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

Council of Science Editors:

-3503-5102. Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/46638

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


University of Texas – Austin

10. -8757-3869. Mass spectrometry combined with strategic enzymatic digestion, selective derivatization and ultraviolet photodissociation for the identification and characterization of Immunoglobulin G antibodies.

Degree: PhD, Chemistry, 2016, University of Texas – Austin

 Immunoglobulin G (IgG) antibodies represent important analytical targets both for their therapeutic properties and for their critical role in the adaptive immune response. While much… (more)

Subjects/Keywords: Mass spectrometry; Antibodies; IgG; Ultraviolet photodissociation

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APA (6th Edition):

-8757-3869. (2016). Mass spectrometry combined with strategic enzymatic digestion, selective derivatization and ultraviolet photodissociation for the identification and characterization of Immunoglobulin G antibodies. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72663

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

Chicago Manual of Style (16th Edition):

-8757-3869. “Mass spectrometry combined with strategic enzymatic digestion, selective derivatization and ultraviolet photodissociation for the identification and characterization of Immunoglobulin G antibodies.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/72663.

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

MLA Handbook (7th Edition):

-8757-3869. “Mass spectrometry combined with strategic enzymatic digestion, selective derivatization and ultraviolet photodissociation for the identification and characterization of Immunoglobulin G antibodies.” 2016. Web. 27 Nov 2020.

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

Vancouver:

-8757-3869. Mass spectrometry combined with strategic enzymatic digestion, selective derivatization and ultraviolet photodissociation for the identification and characterization of Immunoglobulin G antibodies. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/72663.

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

Council of Science Editors:

-8757-3869. Mass spectrometry combined with strategic enzymatic digestion, selective derivatization and ultraviolet photodissociation for the identification and characterization of Immunoglobulin G antibodies. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/72663

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


University of Texas – Austin

11. 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 (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 November 27, 2020. 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. 27 Nov 2020.

Vancouver:

Blazeck JJ. Harnessing Yarrowia lipolytica’s potential as a lipid and alkane production platform. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Nov 27]. 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

12. Gollihar, Jimmy Dale, Jr. Methods in protein engineering and screening : from rational design to directed evolution and beyond.

Degree: PhD, Biochemistry, 2017, University of Texas – Austin

 Humans have engineered organisms for thousands of years. The domestication of plants and animals are early examples of how humans have changed genotypes of organisms… (more)

Subjects/Keywords: Rational design; Directed evolution

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APA (6th Edition):

Gollihar, Jimmy Dale, J. (2017). Methods in protein engineering and screening : from rational design to directed evolution and beyond. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/61769

Chicago Manual of Style (16th Edition):

Gollihar, Jimmy Dale, Jr. “Methods in protein engineering and screening : from rational design to directed evolution and beyond.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/61769.

MLA Handbook (7th Edition):

Gollihar, Jimmy Dale, Jr. “Methods in protein engineering and screening : from rational design to directed evolution and beyond.” 2017. Web. 27 Nov 2020.

Vancouver:

Gollihar, Jimmy Dale J. Methods in protein engineering and screening : from rational design to directed evolution and beyond. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/61769.

Council of Science Editors:

Gollihar, Jimmy Dale J. Methods in protein engineering and screening : from rational design to directed evolution and beyond. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/61769


University of Texas – Austin

13. Bowen, Kimberly Elizabeth. Designing proteasome adaptors to deplete specific proteins from cells.

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

 Cellular protein levels are governed by their rates of synthesis and degradation, and both processes are intricately regulated. One way to study the role of… (more)

Subjects/Keywords: Proteasome; Degradation; Shp2; Abl

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APA (6th Edition):

Bowen, K. E. (2019). Designing proteasome adaptors to deplete specific proteins from cells. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2174

Chicago Manual of Style (16th Edition):

Bowen, Kimberly Elizabeth. “Designing proteasome adaptors to deplete specific proteins from cells.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://dx.doi.org/10.26153/tsw/2174.

MLA Handbook (7th Edition):

Bowen, Kimberly Elizabeth. “Designing proteasome adaptors to deplete specific proteins from cells.” 2019. Web. 27 Nov 2020.

Vancouver:

Bowen KE. Designing proteasome adaptors to deplete specific proteins from cells. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2020 Nov 27]. Available from: http://dx.doi.org/10.26153/tsw/2174.

Council of Science Editors:

Bowen KE. Designing proteasome adaptors to deplete specific proteins from cells. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2174


University of Texas – Austin

14. Kim, Hyo Kyung. A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses.

Degree: PhD, Cell and molecular biology, 2016, University of Texas – Austin

 Bacteria use diverse nucleotide-based small molecules as second messengers to transduce various signals in their extra- and intracellular conditions, and to elicit appropriate cellular responses.… (more)

Subjects/Keywords: YfiN; C-di-GMP; FtsZ; Cell division; Envelope stress

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APA (6th Edition):

Kim, H. K. (2016). A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46436

Chicago Manual of Style (16th Edition):

Kim, Hyo Kyung. “A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/46436.

MLA Handbook (7th Edition):

Kim, Hyo Kyung. “A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses.” 2016. Web. 27 Nov 2020.

Vancouver:

Kim HK. A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/46436.

Council of Science Editors:

Kim HK. A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/46436


University of Texas – Austin

15. Hernandez, Derek Scott. Multiphoton techniques for dynamic manipulation of cellular microenvironments.

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

 A multitude of biophysical signals, including chemical, mechanical, and contact guidance cues, are embedded within the extracellular matrix (ECM) to dictate cell behavior and determine… (more)

Subjects/Keywords: Dynamic cell culture; Hydrogels; Biomaterials; Schwann cells; Immobilization; Chemical gradients; Stiffness gradients

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APA (6th Edition):

Hernandez, D. S. (2014). Multiphoton techniques for dynamic manipulation of cellular microenvironments. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31299

Chicago Manual of Style (16th Edition):

Hernandez, Derek Scott. “Multiphoton techniques for dynamic manipulation of cellular microenvironments.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/31299.

MLA Handbook (7th Edition):

Hernandez, Derek Scott. “Multiphoton techniques for dynamic manipulation of cellular microenvironments.” 2014. Web. 27 Nov 2020.

Vancouver:

Hernandez DS. Multiphoton techniques for dynamic manipulation of cellular microenvironments. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/31299.

Council of Science Editors:

Hernandez DS. Multiphoton techniques for dynamic manipulation of cellular microenvironments. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31299


University of Texas – Austin

16. 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 November 27, 2020. 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. 27 Nov 2020.

Vancouver:

Lanza AM. Novel tools for engineering eukaryotic cells using a systems level approach. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Nov 27]. 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

17. -5682-1161. High throughput methods for measuring TCR-pMHC affinity and specificity.

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

 T cells are a crucial component of the human immune response. I developed two technology platforms that enable high-throughput measurement of TCR-pMHC affinity, sequence, and… (more)

Subjects/Keywords: Immunology; T cell

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APA (6th Edition):

-5682-1161. (2017). High throughput methods for measuring TCR-pMHC affinity and specificity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/7530

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-5682-1161. “High throughput methods for measuring TCR-pMHC affinity and specificity.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://dx.doi.org/10.26153/tsw/7530.

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

MLA Handbook (7th Edition):

-5682-1161. “High throughput methods for measuring TCR-pMHC affinity and specificity.” 2017. Web. 27 Nov 2020.

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

Vancouver:

-5682-1161. High throughput methods for measuring TCR-pMHC affinity and specificity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Nov 27]. Available from: http://dx.doi.org/10.26153/tsw/7530.

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

Council of Science Editors:

-5682-1161. High throughput methods for measuring TCR-pMHC affinity and specificity. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/7530

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


University of Texas – Austin

18. Young, Eric Mosher. Transporter engineering as a tool for metabolic engineering.

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

 The purpose of metabolic engineering is to understand, design, and optimize metabolism. The objective is chemicals synthesis by microbes. To fulfill this purpose and achieve… (more)

Subjects/Keywords: Metabolic engineering; Xylose metabolism; Protein engineering; Transport proteins; Yeast; Synthetic biology

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APA (6th Edition):

Young, E. M. (2013). Transporter engineering as a tool for metabolic engineering. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/35386

Chicago Manual of Style (16th Edition):

Young, Eric Mosher. “Transporter engineering as a tool for metabolic engineering.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/35386.

MLA Handbook (7th Edition):

Young, Eric Mosher. “Transporter engineering as a tool for metabolic engineering.” 2013. Web. 27 Nov 2020.

Vancouver:

Young EM. Transporter engineering as a tool for metabolic engineering. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/35386.

Council of Science Editors:

Young EM. Transporter engineering as a tool for metabolic engineering. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/35386


University of Texas – Austin

19. -6896-3354. Analyzing infection-driven immune perturbations by quantitative IR-Seq.

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

 Immune repertoire sequencing (IR-Seq) rapidly emerged with the advent of high-throughput sequencing as a means of characterizing the adaptive immune system. Early generations of IR-Seq… (more)

Subjects/Keywords: Systems immunology; Antibodies; T cells; Immune repertoire sequencing; Antibody repertoire sequencing; TCR repertoire sequencing; Malaria; Plasmodium falciparum; HIV; Follicular helper T cells; Infant immunity

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APA (6th Edition):

-6896-3354. (2017). Analyzing infection-driven immune perturbations by quantitative IR-Seq. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63463

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

Chicago Manual of Style (16th Edition):

-6896-3354. “Analyzing infection-driven immune perturbations by quantitative IR-Seq.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/63463.

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

MLA Handbook (7th Edition):

-6896-3354. “Analyzing infection-driven immune perturbations by quantitative IR-Seq.” 2017. Web. 27 Nov 2020.

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

Vancouver:

-6896-3354. Analyzing infection-driven immune perturbations by quantitative IR-Seq. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/63463.

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

Council of Science Editors:

-6896-3354. Analyzing infection-driven immune perturbations by quantitative IR-Seq. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://hdl.handle.net/2152/63463

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


University of Texas – Austin

20. -5150-4984. Beyond protein factories : expanding the synthetic biology toolkit for engineering mammalian hosts.

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

 The incredible clinical and commercial successes of recombinant protein therapeutics cemented the use of mammalian cells as the premier production hosts for these products. However,… (more)

Subjects/Keywords: Mammalian cell engineering; Promoter engineering; Terminator engineering

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

APA (6th Edition):

-5150-4984. (2017). Beyond protein factories : expanding the synthetic biology toolkit for engineering mammalian hosts. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/7428

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

Chicago Manual of Style (16th Edition):

-5150-4984. “Beyond protein factories : expanding the synthetic biology toolkit for engineering mammalian hosts.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://dx.doi.org/10.26153/tsw/7428.

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

MLA Handbook (7th Edition):

-5150-4984. “Beyond protein factories : expanding the synthetic biology toolkit for engineering mammalian hosts.” 2017. Web. 27 Nov 2020.

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

Vancouver:

-5150-4984. Beyond protein factories : expanding the synthetic biology toolkit for engineering mammalian hosts. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2020 Nov 27]. Available from: http://dx.doi.org/10.26153/tsw/7428.

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

Council of Science Editors:

-5150-4984. Beyond protein factories : expanding the synthetic biology toolkit for engineering mammalian hosts. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/7428

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


University of Texas – Austin

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

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 November 27, 2020. 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. 27 Nov 2020.

Vancouver:

Crook NC. Novel approaches for metabolic engineering of yeast at multiple scales. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 27]. 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


University of Texas – Austin

22. Curran, Kathleen Anne. Optimizing gene expression in saccharomyces cerevisiae for metabolic engineering applications.

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

 Metabolic engineering has enabled the advancement of biotechnology over the past few decades through the use of cells as biochemical factories. Cellular factories have now… (more)

Subjects/Keywords: Metabolic engineering; Saccharomyces cerevisiae; Yeast; Promoter; Muconic acid; Terminator; Plasmid

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APA (6th Edition):

Curran, K. A. (2014). Optimizing gene expression in saccharomyces cerevisiae for metabolic engineering applications. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30469

Chicago Manual of Style (16th Edition):

Curran, Kathleen Anne. “Optimizing gene expression in saccharomyces cerevisiae for metabolic engineering applications.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/30469.

MLA Handbook (7th Edition):

Curran, Kathleen Anne. “Optimizing gene expression in saccharomyces cerevisiae for metabolic engineering applications.” 2014. Web. 27 Nov 2020.

Vancouver:

Curran KA. Optimizing gene expression in saccharomyces cerevisiae for metabolic engineering applications. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/30469.

Council of Science Editors:

Curran KA. Optimizing gene expression in saccharomyces cerevisiae for metabolic engineering applications. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/30469


University of Texas – Austin

23. Dekosky, Brandon James. Decoding the antibody repertoire : high throughput sequencing of multiple transcripts from single B cells.

Degree: PhD, Chemical Engineering, 2015, University of Texas – Austin

 Next-generation (high throughput) DNA sequencing of immunoglobulin variable region and T-cell receptor gene repertoires is providing critical information for understanding adaptive immune responses and for… (more)

Subjects/Keywords: Antibody; B cell; High-throughput sequencing; Immunology; Biotechnology

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APA (6th Edition):

Dekosky, B. J. (2015). Decoding the antibody repertoire : high throughput sequencing of multiple transcripts from single B cells. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46538

Chicago Manual of Style (16th Edition):

Dekosky, Brandon James. “Decoding the antibody repertoire : high throughput sequencing of multiple transcripts from single B cells.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/46538.

MLA Handbook (7th Edition):

Dekosky, Brandon James. “Decoding the antibody repertoire : high throughput sequencing of multiple transcripts from single B cells.” 2015. Web. 27 Nov 2020.

Vancouver:

Dekosky BJ. Decoding the antibody repertoire : high throughput sequencing of multiple transcripts from single B cells. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/46538.

Council of Science Editors:

Dekosky BJ. Decoding the antibody repertoire : high throughput sequencing of multiple transcripts from single B cells. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46538


University of Texas – Austin

24. Tsai, Chen-Hsun. Identification and characterization of novel regulatory small RNAs in Deinococcus radiodurans.

Degree: PhD, Chemical Engineering, 2020, University of Texas – Austin

 Gene expression regulation mechanisms during stress recovery are ubiquitous across all organisms. Some organisms have evolved more robust and distinct regulatory systems to survive exposures… (more)

Subjects/Keywords: Small RNA; Deinococcus radiodurans; Transcriptome; Extremophile; Ionizing radiation; Radioresistance

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APA (6th Edition):

Tsai, C. (2020). Identification and characterization of novel regulatory small RNAs in Deinococcus radiodurans. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/7430

Chicago Manual of Style (16th Edition):

Tsai, Chen-Hsun. “Identification and characterization of novel regulatory small RNAs in Deinococcus radiodurans.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://dx.doi.org/10.26153/tsw/7430.

MLA Handbook (7th Edition):

Tsai, Chen-Hsun. “Identification and characterization of novel regulatory small RNAs in Deinococcus radiodurans.” 2020. Web. 27 Nov 2020.

Vancouver:

Tsai C. Identification and characterization of novel regulatory small RNAs in Deinococcus radiodurans. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Nov 27]. Available from: http://dx.doi.org/10.26153/tsw/7430.

Council of Science Editors:

Tsai C. Identification and characterization of novel regulatory small RNAs in Deinococcus radiodurans. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/7430


University of Texas – Austin

25. Ooi, Tracy Peksim. The generation of antigen-specific CD8+ T cells from stem cells for adoptive transfer immunotherapy.

Degree: PhD, Cell and Molecular Biology, 2014, University of Texas – Austin

 Adoptive T cell transfer is a form of immunotherapy that has shown promise in treating several cancers and post-transplant lymphoproliferative diseases. This therapy relies on… (more)

Subjects/Keywords: Cytotoxic T cells; CD34+ cord blood; Notch ligands; MHC/HLA tetramers; T cell development; Adoptive T cell transfer; Immunotherapy

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

APA (6th Edition):

Ooi, T. P. (2014). The generation of antigen-specific CD8+ T cells from stem cells for adoptive transfer immunotherapy. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63851

Chicago Manual of Style (16th Edition):

Ooi, Tracy Peksim. “The generation of antigen-specific CD8+ T cells from stem cells for adoptive transfer immunotherapy.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/63851.

MLA Handbook (7th Edition):

Ooi, Tracy Peksim. “The generation of antigen-specific CD8+ T cells from stem cells for adoptive transfer immunotherapy.” 2014. Web. 27 Nov 2020.

Vancouver:

Ooi TP. The generation of antigen-specific CD8+ T cells from stem cells for adoptive transfer immunotherapy. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/63851.

Council of Science Editors:

Ooi TP. The generation of antigen-specific CD8+ T cells from stem cells for adoptive transfer immunotherapy. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/63851


University of Texas – Austin

26. Carroll, Sean Matthew. Strategies for generating therapeutic antibodies.

Degree: PhD, Chemical Engineering, 2012, University of Texas – Austin

 Monoclonal antibodies have become essential therapeutic tools and currently dominate the therapeutic protein market. Consequently, there is continued demand for new therapeutic antibodies and their… (more)

Subjects/Keywords: Antibodies

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APA (6th Edition):

Carroll, S. M. (2012). Strategies for generating therapeutic antibodies. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2012-08-5990

Chicago Manual of Style (16th Edition):

Carroll, Sean Matthew. “Strategies for generating therapeutic antibodies.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/ETD-UT-2012-08-5990.

MLA Handbook (7th Edition):

Carroll, Sean Matthew. “Strategies for generating therapeutic antibodies.” 2012. Web. 27 Nov 2020.

Vancouver:

Carroll SM. Strategies for generating therapeutic antibodies. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/ETD-UT-2012-08-5990.

Council of Science Editors:

Carroll SM. Strategies for generating therapeutic antibodies. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/ETD-UT-2012-08-5990


University of Texas – Austin

27. 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 November 27, 2020. 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. 27 Nov 2020.

Vancouver:

Wang, Bo PDice. High-throughput analysis of native antibody repertoires for therapeutics discovery. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. 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

28. -0618-2971. Developing novel tools to characterize regulatory RNA-protein networks in vivo.

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

 This work focuses on the design and implementation of tools to characterize a regulatory RNA-protein network in vivo. As such, this work developed techniques to… (more)

Subjects/Keywords: Carbon storage regulator; Post-transcriptional regulation; In vivo interaction detection

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APA (6th Edition):

-0618-2971. (2016). Developing novel tools to characterize regulatory RNA-protein networks in vivo. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72694

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-0618-2971. “Developing novel tools to characterize regulatory RNA-protein networks in vivo.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://hdl.handle.net/2152/72694.

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

MLA Handbook (7th Edition):

-0618-2971. “Developing novel tools to characterize regulatory RNA-protein networks in vivo.” 2016. Web. 27 Nov 2020.

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

Vancouver:

-0618-2971. Developing novel tools to characterize regulatory RNA-protein networks in vivo. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2152/72694.

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

Council of Science Editors:

-0618-2971. Developing novel tools to characterize regulatory RNA-protein networks in vivo. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/72694

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


University of Texas – Austin

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

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 November 27, 2020. 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. 27 Nov 2020.

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 2020 Nov 27]. 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


University of Texas – Austin

30. -1345-6122. A yeast-based assay for protein tyrosine kinase substrate specificity and inhibitor resistance.

Degree: PhD, Biochemistry, 2020, University of Texas – Austin

 Phosphorylation of tyrosines by protein kinases is a fundamental mode of signal transduction in all eukaryotic cells, leading to a wide variety of cellular outcomes,… (more)

Subjects/Keywords: Kinase; TKI; Substrate specificity; ABL; BCR-ABL; Imatinib; Dasatinib; Ponatinib; Erlotinib; Resistance; Acquired resistance

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

APA (6th Edition):

-1345-6122. (2020). A yeast-based assay for protein tyrosine kinase substrate specificity and inhibitor resistance. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/7450

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

Chicago Manual of Style (16th Edition):

-1345-6122. “A yeast-based assay for protein tyrosine kinase substrate specificity and inhibitor resistance.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed November 27, 2020. http://dx.doi.org/10.26153/tsw/7450.

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

MLA Handbook (7th Edition):

-1345-6122. “A yeast-based assay for protein tyrosine kinase substrate specificity and inhibitor resistance.” 2020. Web. 27 Nov 2020.

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

Vancouver:

-1345-6122. A yeast-based assay for protein tyrosine kinase substrate specificity and inhibitor resistance. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Nov 27]. Available from: http://dx.doi.org/10.26153/tsw/7450.

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

Council of Science Editors:

-1345-6122. A yeast-based assay for protein tyrosine kinase substrate specificity and inhibitor resistance. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/7450

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

[1] [2] [3]

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