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You searched for +publisher:"University of Texas – Austin" +contributor:("Dalby, Kevin"). Showing records 1 – 28 of 28 total matches.

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University of Texas – Austin

1. Devkota, Ashwini Kumar. Mechanistic studies and drug discovery for eEF-2 kinase.

Degree: PhD, Cell and Molecular Biology, 2011, University of Texas – Austin

 eEF-2K, also known as CaM kinase-III, is an atypical protein kinase which negatively regulates the global rate of protein synthesis through the phosphorylation and inactivation… (more)

Subjects/Keywords: eEF-2 kinase; eEF-2K; Cancer; High-throughput screen; Drug discovery

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APA (6th Edition):

Devkota, A. K. (2011). Mechanistic studies and drug discovery for eEF-2 kinase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22246

Chicago Manual of Style (16th Edition):

Devkota, Ashwini Kumar. “Mechanistic studies and drug discovery for eEF-2 kinase.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/22246.

MLA Handbook (7th Edition):

Devkota, Ashwini Kumar. “Mechanistic studies and drug discovery for eEF-2 kinase.” 2011. Web. 11 Apr 2021.

Vancouver:

Devkota AK. Mechanistic studies and drug discovery for eEF-2 kinase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/22246.

Council of Science Editors:

Devkota AK. Mechanistic studies and drug discovery for eEF-2 kinase. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/22246


University of Texas – Austin

2. -5244-803X. Biomechanical regulation of cancer metastasis.

Degree: PhD, Biomedical Engineering, 2018, University of Texas – Austin

 Metastasis is the ultimate cause of most cancer-related deaths. As such, it is critical to understand the processes that control the spread of cancer through… (more)

Subjects/Keywords: Metastasis; Mechanical strain; Shear stress

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APA (6th Edition):

-5244-803X. (2018). Biomechanical regulation of cancer metastasis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/10181

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

Chicago Manual of Style (16th Edition):

-5244-803X. “Biomechanical regulation of cancer metastasis.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://dx.doi.org/10.26153/tsw/10181.

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

MLA Handbook (7th Edition):

-5244-803X. “Biomechanical regulation of cancer metastasis.” 2018. Web. 11 Apr 2021.

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

Vancouver:

-5244-803X. Biomechanical regulation of cancer metastasis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2021 Apr 11]. Available from: http://dx.doi.org/10.26153/tsw/10181.

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

Council of Science Editors:

-5244-803X. Biomechanical regulation of cancer metastasis. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://dx.doi.org/10.26153/tsw/10181

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


University of Texas – Austin

3. Mand, Michael Rodgers. Mechanisms and consequences of ATM activation.

Degree: PhD, Cellular and Molecular Biology, 2015, University of Texas – Austin

 Mutations in the ataxia telangiectasia mutated (ATM) gene cause the disease ataxia-telangiectasia (A-T). Patients with this disease have multiple symptoms, including the eponymous ataxia and… (more)

Subjects/Keywords: ATM; CK2; Aggregation

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APA (6th Edition):

Mand, M. R. (2015). Mechanisms and consequences of ATM activation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/44484

Chicago Manual of Style (16th Edition):

Mand, Michael Rodgers. “Mechanisms and consequences of ATM activation.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/44484.

MLA Handbook (7th Edition):

Mand, Michael Rodgers. “Mechanisms and consequences of ATM activation.” 2015. Web. 11 Apr 2021.

Vancouver:

Mand MR. Mechanisms and consequences of ATM activation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/44484.

Council of Science Editors:

Mand MR. Mechanisms and consequences of ATM activation. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/44484


University of Texas – Austin

4. Wu, Meilan. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Texas – Austin

 Human PARP-1 is a nuclear protein containing six functional domains that catalyzes the poly(ADP-ribosyl)ation of a variety of protein substrates including itself. This process involves… (more)

Subjects/Keywords: Poly(ADP-ribosyl)ation; PARP-1

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APA (6th Edition):

Wu, M. (2014). DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/62238

Chicago Manual of Style (16th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/62238.

MLA Handbook (7th Edition):

Wu, Meilan. “DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1.” 2014. Web. 11 Apr 2021.

Vancouver:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/62238.

Council of Science Editors:

Wu M. DNA recognition and mechanistic investigation of poly(ADP-ribose) polymerase-1. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/62238


University of Texas – Austin

5. 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 April 11, 2021. 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. 11 Apr 2021.

Vancouver:

Bowen KE. Designing proteasome adaptors to deplete specific proteins from cells. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2021 Apr 11]. 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

6. Spaeth, Christopher Scott. cAMP and oxidative mechanisms of plasmalemmal sealing and the effects on rapid and long lasting repair of severed axons in vivo by polyethylene Glycol.

Degree: PhD, Cell and Molecular Biology, 2011, University of Texas – Austin

 Traumatic neuronal injury inevitably causes plasmalemmal damage, and sometimes leads to axonal severance. For any eukaryotic cell to survive following traumatic injury, the plasmalemma must… (more)

Subjects/Keywords: cAMP; PKA; Epac; Cytosolic oxidation; Polyethylene glycol; Plasmalemmal sealing

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APA (6th Edition):

Spaeth, C. S. (2011). cAMP and oxidative mechanisms of plasmalemmal sealing and the effects on rapid and long lasting repair of severed axons in vivo by polyethylene Glycol. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-05-2670

Chicago Manual of Style (16th Edition):

Spaeth, Christopher Scott. “cAMP and oxidative mechanisms of plasmalemmal sealing and the effects on rapid and long lasting repair of severed axons in vivo by polyethylene Glycol.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/ETD-UT-2011-05-2670.

MLA Handbook (7th Edition):

Spaeth, Christopher Scott. “cAMP and oxidative mechanisms of plasmalemmal sealing and the effects on rapid and long lasting repair of severed axons in vivo by polyethylene Glycol.” 2011. Web. 11 Apr 2021.

Vancouver:

Spaeth CS. cAMP and oxidative mechanisms of plasmalemmal sealing and the effects on rapid and long lasting repair of severed axons in vivo by polyethylene Glycol. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-05-2670.

Council of Science Editors:

Spaeth CS. cAMP and oxidative mechanisms of plasmalemmal sealing and the effects on rapid and long lasting repair of severed axons in vivo by polyethylene Glycol. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-05-2670


University of Texas – Austin

7. Tavares, Clint Damian Jaxon. Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation.

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

 Eukaryotic elongation factor 2 kinase (eEF-2K) is an atypical calcium/calmodulin-dependent protein kinase (CaMK-III). The kinase provides a mechanism by which cells can globally control the… (more)

Subjects/Keywords: Elongation factor 2 kinase (eEF-2K); Calmodulin; Kinase; Protein synthesis; Calcium; eEF-2, Autophosphorylation; Thr-348; Ser-500

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APA (6th Edition):

Tavares, C. D. J. (2014). Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47184

Chicago Manual of Style (16th Edition):

Tavares, Clint Damian Jaxon. “Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/47184.

MLA Handbook (7th Edition):

Tavares, Clint Damian Jaxon. “Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation.” 2014. Web. 11 Apr 2021.

Vancouver:

Tavares CDJ. Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/47184.

Council of Science Editors:

Tavares CDJ. Regulation of elongation factor 2 kinase (eEF-2K) by phosphorylation. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/47184


University of Texas – Austin

8. -8962-3030. Regulation of elongation factor 2 kinase (eEF-2K) by acidity.

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

 Eukaryotic elongation factor 2 kinase (eEF-2K) is a calmodulin (CaM)/calcium regulated kinase whose activity disrupts translation elongation resulting in the global decrease of protein synthesis¹.… (more)

Subjects/Keywords: eEF-2K; Acidity; Elongation factor 2 kinase

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APA (6th Edition):

-8962-3030. (2019). Regulation of elongation factor 2 kinase (eEF-2K) by acidity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72809

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

Chicago Manual of Style (16th Edition):

-8962-3030. “Regulation of elongation factor 2 kinase (eEF-2K) by acidity.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/72809.

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

MLA Handbook (7th Edition):

-8962-3030. “Regulation of elongation factor 2 kinase (eEF-2K) by acidity.” 2019. Web. 11 Apr 2021.

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

Vancouver:

-8962-3030. Regulation of elongation factor 2 kinase (eEF-2K) by acidity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/72809.

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

Council of Science Editors:

-8962-3030. Regulation of elongation factor 2 kinase (eEF-2K) by acidity. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://hdl.handle.net/2152/72809

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


University of Texas – Austin

9. Ebelt, Nancy Danielle. The covalent JNK inhibitor, JNK-in-8, synergizes with lapatinib to cause cell death in basal-like breast cancer cell lines.

Degree: PhD, Cell and Molecular Biology, 2015, University of Texas – Austin

 Basal-like and Claudin-low breast cancers have the worst prognosis and represent 15-20% of breast cancers diagnosed each year. Endocrine and molecularly targeted therapies are ineffective… (more)

Subjects/Keywords: Basal-like; JNK; JNK-IN-8; Lapatinib; Breast cancer

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APA (6th Edition):

Ebelt, N. D. (2015). The covalent JNK inhibitor, JNK-in-8, synergizes with lapatinib to cause cell death in basal-like breast cancer cell lines. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46808

Chicago Manual of Style (16th Edition):

Ebelt, Nancy Danielle. “The covalent JNK inhibitor, JNK-in-8, synergizes with lapatinib to cause cell death in basal-like breast cancer cell lines.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/46808.

MLA Handbook (7th Edition):

Ebelt, Nancy Danielle. “The covalent JNK inhibitor, JNK-in-8, synergizes with lapatinib to cause cell death in basal-like breast cancer cell lines.” 2015. Web. 11 Apr 2021.

Vancouver:

Ebelt ND. The covalent JNK inhibitor, JNK-in-8, synergizes with lapatinib to cause cell death in basal-like breast cancer cell lines. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/46808.

Council of Science Editors:

Ebelt ND. The covalent JNK inhibitor, JNK-in-8, synergizes with lapatinib to cause cell death in basal-like breast cancer cell lines. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46808


University of Texas – Austin

10. -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 (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 April 11, 2021. 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. 11 Apr 2021.

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 2021 Apr 11]. 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

11. -5604-9810. Advancement of photodissociation mass spectrometry methods for the analysis of protein post-translational modifications.

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

 Post-translational modifications (PTMs) are important for regulating protein structure and function. Despite significant progress for PTM analysis using liquid chromatography tandem mass spectrometry (LC-MS/MS), opportunities… (more)

Subjects/Keywords: Mass spectrometry; Ultraviolet photodissociation; Proteomics; Phosphorylation; Sulfation

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APA (6th Edition):

-5604-9810. (2018). Advancement of photodissociation mass spectrometry methods for the analysis of protein post-translational modifications. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68369

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

Chicago Manual of Style (16th Edition):

-5604-9810. “Advancement of photodissociation mass spectrometry methods for the analysis of protein post-translational modifications.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/68369.

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

MLA Handbook (7th Edition):

-5604-9810. “Advancement of photodissociation mass spectrometry methods for the analysis of protein post-translational modifications.” 2018. Web. 11 Apr 2021.

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

Vancouver:

-5604-9810. Advancement of photodissociation mass spectrometry methods for the analysis of protein post-translational modifications. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/68369.

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

Council of Science Editors:

-5604-9810. Advancement of photodissociation mass spectrometry methods for the analysis of protein post-translational modifications. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68369

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


University of Texas – Austin

12. Zamora Olivares, Diana Paulina. Differential sensing of kinases.

Degree: PhD, Organic Chemistry, 2014, University of Texas – Austin

 During the last decade, organic and supramolecular chemistry in combination with analytical and fluorescent-based sensing methods have led to the development of chemical biology tools… (more)

Subjects/Keywords: Chemosensors; Kinases

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APA (6th Edition):

Zamora Olivares, D. P. (2014). Differential sensing of kinases. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30454

Chicago Manual of Style (16th Edition):

Zamora Olivares, Diana Paulina. “Differential sensing of kinases.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/30454.

MLA Handbook (7th Edition):

Zamora Olivares, Diana Paulina. “Differential sensing of kinases.” 2014. Web. 11 Apr 2021.

Vancouver:

Zamora Olivares DP. Differential sensing of kinases. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/30454.

Council of Science Editors:

Zamora Olivares DP. Differential sensing of kinases. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/30454


University of Texas – Austin

13. Ziehr, Jessica Lea. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.

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

 The human mitochondrial DNA (mtDNA) genome must be faithfully maintained by the mitochondrial DNA replication machinery. Deficiencies in mtDNA maintenance result in the accumulation of… (more)

Subjects/Keywords: DNA polymerase; Pre-steady state kinetics; HIV reverse transcriptase; Polymerase gamma

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APA (6th Edition):

Ziehr, J. L. (2014). Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31296

Chicago Manual of Style (16th Edition):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/31296.

MLA Handbook (7th Edition):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Web. 11 Apr 2021.

Vancouver:

Ziehr JL. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/31296.

Council of Science Editors:

Ziehr JL. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31296


University of Texas – Austin

14. Park, Jihyun. Regulation and function of two membrane-associated protein kinases.

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

 Protein kinases, many of which are regulated by autophosphorylation, modify their substrates by phosphorylation. Due to their roles in cellular signaling cascades controlling processes such… (more)

Subjects/Keywords: Kinase; TRPM7; Autophosphorylation; UPR; PERK; Cancer

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APA (6th Edition):

Park, J. (2014). Regulation and function of two membrane-associated protein kinases. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/47189

Chicago Manual of Style (16th Edition):

Park, Jihyun. “Regulation and function of two membrane-associated protein kinases.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/47189.

MLA Handbook (7th Edition):

Park, Jihyun. “Regulation and function of two membrane-associated protein kinases.” 2014. Web. 11 Apr 2021.

Vancouver:

Park J. Regulation and function of two membrane-associated protein kinases. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/47189.

Council of Science Editors:

Park J. Regulation and function of two membrane-associated protein kinases. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/47189

15. Kaoud, Tamer Saad Gabr. Regulation and inhibition of MAP kinases.

Degree: PhD, Pharmacy, 2012, University of Texas – Austin

 Due to their role in cellular signaling, mitogen activated protein (MAP) kinases represent targets of pharmaceutical interest. Most MAP kinase inhibitors target the highly conserved… (more)

Subjects/Keywords: MAP; Kinases; Inhibition; Regulation

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APA (6th Edition):

Kaoud, T. S. G. (2012). Regulation and inhibition of MAP kinases. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22188

Chicago Manual of Style (16th Edition):

Kaoud, Tamer Saad Gabr. “Regulation and inhibition of MAP kinases.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/22188.

MLA Handbook (7th Edition):

Kaoud, Tamer Saad Gabr. “Regulation and inhibition of MAP kinases.” 2012. Web. 11 Apr 2021.

Vancouver:

Kaoud TSG. Regulation and inhibition of MAP kinases. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/22188.

Council of Science Editors:

Kaoud TSG. Regulation and inhibition of MAP kinases. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/22188


University of Texas – Austin

16. Callaway, Kari-Kristin Anderson. Mechanism and regulation of the protein kinase ERK2.

Degree: PhD, Biochemistry, 2006, University of Texas – Austin

 The extracellular signal-regulated kinase 2 (ERK2) cascade plays important roles in a variety of cellular events such as proliferation, differentiation, and apoptosis. Involvement in such… (more)

Subjects/Keywords: Protein kinase CK2; Protein binding

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APA (6th Edition):

Callaway, K. A. (2006). Mechanism and regulation of the protein kinase ERK2. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/2470

Chicago Manual of Style (16th Edition):

Callaway, Kari-Kristin Anderson. “Mechanism and regulation of the protein kinase ERK2.” 2006. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/2470.

MLA Handbook (7th Edition):

Callaway, Kari-Kristin Anderson. “Mechanism and regulation of the protein kinase ERK2.” 2006. Web. 11 Apr 2021.

Vancouver:

Callaway KA. Mechanism and regulation of the protein kinase ERK2. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2006. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/2470.

Council of Science Editors:

Callaway KA. Mechanism and regulation of the protein kinase ERK2. [Doctoral Dissertation]. University of Texas – Austin; 2006. Available from: http://hdl.handle.net/2152/2470


University of Texas – Austin

17. Rainey, Mark Allan. A structure/function analysis of macromolecular recognition by the protein kinase ERK2.

Degree: PhD, Molecular Biology, 2004, University of Texas – Austin

 Mitogen-activate protein kinases (MAPKs) phosphorylate protein substrates in the presence of magnesium and adenosine triphosphate in response to extracellular environmental signals to carry out signal-dependent… (more)

Subjects/Keywords: Protein kinase ERK2; Protein binding

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APA (6th Edition):

Rainey, M. A. (2004). A structure/function analysis of macromolecular recognition by the protein kinase ERK2. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/1392

Chicago Manual of Style (16th Edition):

Rainey, Mark Allan. “A structure/function analysis of macromolecular recognition by the protein kinase ERK2.” 2004. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/1392.

MLA Handbook (7th Edition):

Rainey, Mark Allan. “A structure/function analysis of macromolecular recognition by the protein kinase ERK2.” 2004. Web. 11 Apr 2021.

Vancouver:

Rainey MA. A structure/function analysis of macromolecular recognition by the protein kinase ERK2. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2004. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/1392.

Council of Science Editors:

Rainey MA. A structure/function analysis of macromolecular recognition by the protein kinase ERK2. [Doctoral Dissertation]. University of Texas – Austin; 2004. Available from: http://hdl.handle.net/2152/1392

18. Harger, Matthew Thomas. Development and analysis of Tinker-OpenMM as a GPU-based free energy perturbation engine.

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

 The utilization of computational technologies for the lead optimization process is one of the biggest challenges in the computational chemistry field. In this dissertation, I… (more)

Subjects/Keywords: Energy perturbation engine; Tinker-OpenMM

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APA (6th Edition):

Harger, M. T. (2019). Development and analysis of Tinker-OpenMM as a GPU-based free energy perturbation engine. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/3259

Chicago Manual of Style (16th Edition):

Harger, Matthew Thomas. “Development and analysis of Tinker-OpenMM as a GPU-based free energy perturbation engine.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://dx.doi.org/10.26153/tsw/3259.

MLA Handbook (7th Edition):

Harger, Matthew Thomas. “Development and analysis of Tinker-OpenMM as a GPU-based free energy perturbation engine.” 2019. Web. 11 Apr 2021.

Vancouver:

Harger MT. Development and analysis of Tinker-OpenMM as a GPU-based free energy perturbation engine. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2021 Apr 11]. Available from: http://dx.doi.org/10.26153/tsw/3259.

Council of Science Editors:

Harger MT. Development and analysis of Tinker-OpenMM as a GPU-based free energy perturbation engine. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/3259

19. -2780-6317. Mechanisms of target search by DNA-binding proteins.

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

 All genetic information is preserved within the DNA duplex. For successful propagation of this genetic code, DNA must be accurately replicated, repaired, and transcribed. These… (more)

Subjects/Keywords: DNA repair; MMR; CRISPR; Single-Molecule; Biophysics

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APA (6th Edition):

-2780-6317. (2018). Mechanisms of target search by DNA-binding proteins. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68160

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2780-6317. “Mechanisms of target search by DNA-binding proteins.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/68160.

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

MLA Handbook (7th Edition):

-2780-6317. “Mechanisms of target search by DNA-binding proteins.” 2018. Web. 11 Apr 2021.

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

Vancouver:

-2780-6317. Mechanisms of target search by DNA-binding proteins. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/68160.

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

Council of Science Editors:

-2780-6317. Mechanisms of target search by DNA-binding proteins. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68160

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Author name may be incomplete

20. Zuzek, Aleksej. Diacylglycerol, novel protein kinase C isozymes [eta] and [theta], and other diacylglycerol activated proteins promote neuroprotective plasmalemmal sealing in B104 neurons in vitro and rat sciatic nerve axons in vivo.

Degree: PhD, Cell and Molecular Biology, 2012, University of Texas – Austin

 To survive, neurons and other eukaryotic cells must rapidly repair (seal) plasmalemmal damage. Such repair occurs by an accumulation of intracellular vesicles at or near… (more)

Subjects/Keywords: Protein kinase C (PKC); Diacylglycerol (DAG); Protein kinase A (PKA); Cyclic AMP (cAMP); Myristoylated alanine rich C kinase substrate (MARCKS); Munc13; Polyethylene glycol (PEG); Plasmalemma; Plasmalemma disruptions; Plasmalemmal sealing; Survival; Peripheral nerve injury; Stroke

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APA (6th Edition):

Zuzek, A. (2012). Diacylglycerol, novel protein kinase C isozymes [eta] and [theta], and other diacylglycerol activated proteins promote neuroprotective plasmalemmal sealing in B104 neurons in vitro and rat sciatic nerve axons in vivo. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/19576

Chicago Manual of Style (16th Edition):

Zuzek, Aleksej. “Diacylglycerol, novel protein kinase C isozymes [eta] and [theta], and other diacylglycerol activated proteins promote neuroprotective plasmalemmal sealing in B104 neurons in vitro and rat sciatic nerve axons in vivo.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/19576.

MLA Handbook (7th Edition):

Zuzek, Aleksej. “Diacylglycerol, novel protein kinase C isozymes [eta] and [theta], and other diacylglycerol activated proteins promote neuroprotective plasmalemmal sealing in B104 neurons in vitro and rat sciatic nerve axons in vivo.” 2012. Web. 11 Apr 2021.

Vancouver:

Zuzek A. Diacylglycerol, novel protein kinase C isozymes [eta] and [theta], and other diacylglycerol activated proteins promote neuroprotective plasmalemmal sealing in B104 neurons in vitro and rat sciatic nerve axons in vivo. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/19576.

Council of Science Editors:

Zuzek A. Diacylglycerol, novel protein kinase C isozymes [eta] and [theta], and other diacylglycerol activated proteins promote neuroprotective plasmalemmal sealing in B104 neurons in vitro and rat sciatic nerve axons in vivo. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/19576

21. -8470-1458. Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions.

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

 The unifying topic of this thesis is that of supramolecular and reversible covalent chemistry. Both supramolecular and reversible covalent reactions operate under thermodynamic control, leading… (more)

Subjects/Keywords: Enantiomeric excess; Stereochemistry; Circular dichroism; Supramolecular chemistry; Dynamic combinatorial chemistry; Dynamic covalent reactions

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APA (6th Edition):

-8470-1458. (2017). Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/3114

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8470-1458. “Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions.” 2017. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://dx.doi.org/10.26153/tsw/3114.

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

MLA Handbook (7th Edition):

-8470-1458. “Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions.” 2017. Web. 11 Apr 2021.

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

Vancouver:

-8470-1458. Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2017. [cited 2021 Apr 11]. Available from: http://dx.doi.org/10.26153/tsw/3114.

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

Council of Science Editors:

-8470-1458. Enantiomeric excess determination using circular dichroism spectroscopy and studies of reversible covalent reactions: Enantiomeric excess determination using circular dichroism spectroscopy: Studies of reversible covalent reactions: Study of four orthogonal, reversible covalent reactions. [Doctoral Dissertation]. University of Texas – Austin; 2017. Available from: http://dx.doi.org/10.26153/tsw/3114

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Author name may be incomplete

22. Li, Jing, Ph. D. Dialkynylimidazoles as irreversible MAPK inhibitors, kinase docking site probes, and anti-cancer agents.

Degree: PhD, Pharmacy, 2011, University of Texas – Austin

 This dissertation research was aimed at investigating an interesting class of 1,2-dialkynylimidazoles as: 1. irreversible p38 MAP kinase α-isoform (p38α) inhibitors; 2. p38α docking site… (more)

Subjects/Keywords: Dialkynylimidazoles; Irreversible MAPK inhibitors; Kinase docking site probe; Anti-cancer agents

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APA (6th Edition):

Li, Jing, P. D. (2011). Dialkynylimidazoles as irreversible MAPK inhibitors, kinase docking site probes, and anti-cancer agents. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-08-4070

Chicago Manual of Style (16th Edition):

Li, Jing, Ph D. “Dialkynylimidazoles as irreversible MAPK inhibitors, kinase docking site probes, and anti-cancer agents.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/ETD-UT-2011-08-4070.

MLA Handbook (7th Edition):

Li, Jing, Ph D. “Dialkynylimidazoles as irreversible MAPK inhibitors, kinase docking site probes, and anti-cancer agents.” 2011. Web. 11 Apr 2021.

Vancouver:

Li, Jing PD. Dialkynylimidazoles as irreversible MAPK inhibitors, kinase docking site probes, and anti-cancer agents. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4070.

Council of Science Editors:

Li, Jing PD. Dialkynylimidazoles as irreversible MAPK inhibitors, kinase docking site probes, and anti-cancer agents. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4070

23. -4211-0083. Unconventional approaches to kinase inhibition : covalent inhibitors and docking site inhibitors of mitogen-activated protein kinases.

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

 The body of work that follows is a description of biochemical screening methods to identify non-ATP competitive and covalent ERK inhibitors, as well as assay… (more)

Subjects/Keywords: Kinases; Kinase inhibitors; ERK; JNK; Docking site; Anisotropy; Covalent inhibitor

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APA (6th Edition):

-4211-0083. (2020). Unconventional approaches to kinase inhibition : covalent inhibitors and docking site inhibitors of mitogen-activated protein kinases. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9345

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-4211-0083. “Unconventional approaches to kinase inhibition : covalent inhibitors and docking site inhibitors of mitogen-activated protein kinases.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://dx.doi.org/10.26153/tsw/9345.

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Author name may be incomplete

MLA Handbook (7th Edition):

-4211-0083. “Unconventional approaches to kinase inhibition : covalent inhibitors and docking site inhibitors of mitogen-activated protein kinases.” 2020. Web. 11 Apr 2021.

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

Vancouver:

-4211-0083. Unconventional approaches to kinase inhibition : covalent inhibitors and docking site inhibitors of mitogen-activated protein kinases. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2021 Apr 11]. Available from: http://dx.doi.org/10.26153/tsw/9345.

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

Council of Science Editors:

-4211-0083. Unconventional approaches to kinase inhibition : covalent inhibitors and docking site inhibitors of mitogen-activated protein kinases. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/9345

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Author name may be incomplete

24. Hernandez, Erik Torres. Lessons learned from studying peptide chemistry and the development in mimicking its modularity in the design of a new oligomer using guanidiniums, alpha-diketones, and boronic acids.

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

 Peptide chemistry is a versatile tool in the development of diverse compounds that can be applied in various contexts: biology, drug development, organic synthesis, chemo… (more)

Subjects/Keywords: Peptide chemistry; Selective modification; Single-molecule protein sequencing; Fluorescence sequencing; Unnatural oligomers; Supramolecular oligomers; Unnatural peptides; Unnatural peptide high-ordered arrangement

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APA (6th Edition):

Hernandez, E. T. (2018). Lessons learned from studying peptide chemistry and the development in mimicking its modularity in the design of a new oligomer using guanidiniums, alpha-diketones, and boronic acids. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/63306

Chicago Manual of Style (16th Edition):

Hernandez, Erik Torres. “Lessons learned from studying peptide chemistry and the development in mimicking its modularity in the design of a new oligomer using guanidiniums, alpha-diketones, and boronic acids.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/63306.

MLA Handbook (7th Edition):

Hernandez, Erik Torres. “Lessons learned from studying peptide chemistry and the development in mimicking its modularity in the design of a new oligomer using guanidiniums, alpha-diketones, and boronic acids.” 2018. Web. 11 Apr 2021.

Vancouver:

Hernandez ET. Lessons learned from studying peptide chemistry and the development in mimicking its modularity in the design of a new oligomer using guanidiniums, alpha-diketones, and boronic acids. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/63306.

Council of Science Editors:

Hernandez ET. Lessons learned from studying peptide chemistry and the development in mimicking its modularity in the design of a new oligomer using guanidiniums, alpha-diketones, and boronic acids. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/63306

25. Madsen, James Andrew. Advancement of photodissociation and electron-based tandem mass spectrometry methods for proteome analysis.

Degree: PhD, Analytical Chemistry, 2011, University of Texas – Austin

 The number and types of diagnostic ions obtained by infrared multiphoton dissociation (IRMPD) and collision induced dissociation (CID) were evaluated for supercharged peptide ions created… (more)

Subjects/Keywords: Mass spectrometry; Proteomics; Photodissociation; Electron transfer dissociation

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APA (6th Edition):

Madsen, J. A. (2011). Advancement of photodissociation and electron-based tandem mass spectrometry methods for proteome analysis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-08-3850

Chicago Manual of Style (16th Edition):

Madsen, James Andrew. “Advancement of photodissociation and electron-based tandem mass spectrometry methods for proteome analysis.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/ETD-UT-2011-08-3850.

MLA Handbook (7th Edition):

Madsen, James Andrew. “Advancement of photodissociation and electron-based tandem mass spectrometry methods for proteome analysis.” 2011. Web. 11 Apr 2021.

Vancouver:

Madsen JA. Advancement of photodissociation and electron-based tandem mass spectrometry methods for proteome analysis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-3850.

Council of Science Editors:

Madsen JA. Advancement of photodissociation and electron-based tandem mass spectrometry methods for proteome analysis. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-3850

26. -2576-1079. Activation of caspase-9 within the Apaf-1 apoptosome.

Degree: PhD, Cell and Molecular Biology, 2015, University of Texas – Austin

 A family of cysteinyl aspartate-specific proteases (caspases) induces dramatic biochemical and morphological changes during apoptosis. Initiator caspases are thought to be activated through induced homodimerization,… (more)

Subjects/Keywords: Apoptosis; Caspase-9; Apaf-1; Apoptosome; Auto-catalytic cleavage; Molecular timer; Non-cleavable caspase-9 knock-in mouse

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APA (6th Edition):

-2576-1079. (2015). Activation of caspase-9 within the Apaf-1 apoptosome. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46811

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Author name may be incomplete

Chicago Manual of Style (16th Edition):

-2576-1079. “Activation of caspase-9 within the Apaf-1 apoptosome.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/46811.

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Author name may be incomplete

MLA Handbook (7th Edition):

-2576-1079. “Activation of caspase-9 within the Apaf-1 apoptosome.” 2015. Web. 11 Apr 2021.

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

Vancouver:

-2576-1079. Activation of caspase-9 within the Apaf-1 apoptosome. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/46811.

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

Council of Science Editors:

-2576-1079. Activation of caspase-9 within the Apaf-1 apoptosome. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46811

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Author name may be incomplete


University of Texas – Austin

27. Kellinger, Matthew William. Characterization of HIV-1 Reverse Transcriptase substrate specificity by conformationally sensitive fluorescence.

Degree: PhD, Cell and Molecular Biology, 2010, University of Texas – Austin

 We have engineered a mutant of HIV Reverse Transcriptase that can be fluorescently labeled by covalent attachment of the environmentally sensitive fluorophore 7-diethylamino-3-((((2-maleimidyl)ethyl)amino)carbonyl)coumarin (MDCC). The… (more)

Subjects/Keywords: HIV; Reverse Transcriptase; Induced fit; Drug resistance; Kinetics; Single molecule

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APA (6th Edition):

Kellinger, M. W. (2010). Characterization of HIV-1 Reverse Transcriptase substrate specificity by conformationally sensitive fluorescence. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2010-12-2154

Chicago Manual of Style (16th Edition):

Kellinger, Matthew William. “Characterization of HIV-1 Reverse Transcriptase substrate specificity by conformationally sensitive fluorescence.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/ETD-UT-2010-12-2154.

MLA Handbook (7th Edition):

Kellinger, Matthew William. “Characterization of HIV-1 Reverse Transcriptase substrate specificity by conformationally sensitive fluorescence.” 2010. Web. 11 Apr 2021.

Vancouver:

Kellinger MW. Characterization of HIV-1 Reverse Transcriptase substrate specificity by conformationally sensitive fluorescence. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/ETD-UT-2010-12-2154.

Council of Science Editors:

Kellinger MW. Characterization of HIV-1 Reverse Transcriptase substrate specificity by conformationally sensitive fluorescence. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/ETD-UT-2010-12-2154


University of Texas – Austin

28. George, Andrew Anthony. Calcium-mediated change in neuronal intrinsic excitability in weakly electric fish: biasing mechanisms of homeostatis for those of plasticity.

Degree: PhD, Neuroscience, 2009, University of Texas – Austin

 Although the processes used for temporarily storing and manipulating neural information have been extensively studied at the synaptic level far less attention has been given… (more)

Subjects/Keywords: Electric Fish; Neuronal Intrinsic Excitability; Calcium; Homeostasis; Neuronal Plasticity; PKC; Calcineurin

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APA (6th Edition):

George, A. A. (2009). Calcium-mediated change in neuronal intrinsic excitability in weakly electric fish: biasing mechanisms of homeostatis for those of plasticity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2009-12-407

Chicago Manual of Style (16th Edition):

George, Andrew Anthony. “Calcium-mediated change in neuronal intrinsic excitability in weakly electric fish: biasing mechanisms of homeostatis for those of plasticity.” 2009. Doctoral Dissertation, University of Texas – Austin. Accessed April 11, 2021. http://hdl.handle.net/2152/ETD-UT-2009-12-407.

MLA Handbook (7th Edition):

George, Andrew Anthony. “Calcium-mediated change in neuronal intrinsic excitability in weakly electric fish: biasing mechanisms of homeostatis for those of plasticity.” 2009. Web. 11 Apr 2021.

Vancouver:

George AA. Calcium-mediated change in neuronal intrinsic excitability in weakly electric fish: biasing mechanisms of homeostatis for those of plasticity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2009. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2152/ETD-UT-2009-12-407.

Council of Science Editors:

George AA. Calcium-mediated change in neuronal intrinsic excitability in weakly electric fish: biasing mechanisms of homeostatis for those of plasticity. [Doctoral Dissertation]. University of Texas – Austin; 2009. Available from: http://hdl.handle.net/2152/ETD-UT-2009-12-407

.