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You searched for +publisher:"University of Texas Southwestern Medical Center" +contributor:("Kohler, Jennifer J."). Showing records 1 – 8 of 8 total matches.

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University of Texas Southwestern Medical Center

1. Rodriguez, Andrea Christine. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.

Degree: 2015, University of Texas Southwestern Medical Center

 O-linked β-N-acetylglucosamine (O-GlcNAc) is an abundant post-translational modification that is regulated by two enzymes, O-GlcNAc transferase (OGT) and O-GlcNAc hydrolase (OGA). While it is elusive… (more)

Subjects/Keywords: Acetylglucosamine; Mutation, Missense; N-Acetylglucosaminyltransferases; Nuclear Pore Complex Proteins

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

APA (6th Edition):

Rodriguez, A. C. (2015). Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4449

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

Chicago Manual of Style (16th Edition):

Rodriguez, Andrea Christine. “Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4449.

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

MLA Handbook (7th Edition):

Rodriguez, Andrea Christine. “Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins.” 2015. Web. 09 Jul 2020.

Vancouver:

Rodriguez AC. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4449.

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

Council of Science Editors:

Rodriguez AC. Development of New Photocrosslinking Approaches to Discover Binding Partners of O-GlcNAc-Modified Proteins. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4449

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


University of Texas Southwestern Medical Center

2. Umlauf, Benjamin J. Methods for Identifying Subcellular Targeting Ligands and Selected Applications.

Degree: 2015, University of Texas Southwestern Medical Center

 Subcellular localization plays an essential role in targeting drug therapies as generally the pro-drug or linker relies on physical conditions of a particular subcellular compartment… (more)

Subjects/Keywords: Endocytosis; Lysosomes; Peptides

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APA (6th Edition):

Umlauf, B. J. (2015). Methods for Identifying Subcellular Targeting Ligands and Selected Applications. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4228

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

Chicago Manual of Style (16th Edition):

Umlauf, Benjamin J. “Methods for Identifying Subcellular Targeting Ligands and Selected Applications.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4228.

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

MLA Handbook (7th Edition):

Umlauf, Benjamin J. “Methods for Identifying Subcellular Targeting Ligands and Selected Applications.” 2015. Web. 09 Jul 2020.

Vancouver:

Umlauf BJ. Methods for Identifying Subcellular Targeting Ligands and Selected Applications. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4228.

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

Council of Science Editors:

Umlauf BJ. Methods for Identifying Subcellular Targeting Ligands and Selected Applications. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4228

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


University of Texas Southwestern Medical Center

3. Fermaintt, Charles Steven. TREX1 C-Terminus Regulates Oligosaccharyltransfererase to Prevent the Accumulation of an Endogenous Bioactive Disaccharide Associated with Autoimmune Disorders.

Degree: 2018, University of Texas Southwestern Medical Center

 The innate immune system is the first line of defense against infectious pathogens and serves a vital role in activating the adaptive immune system. Detection… (more)

Subjects/Keywords: Cytosol; Exodeoxyribonucleases; Hexosyltransferases; Membrane Proteins; Phosphoproteins

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APA (6th Edition):

Fermaintt, C. S. (2018). TREX1 C-Terminus Regulates Oligosaccharyltransfererase to Prevent the Accumulation of an Endogenous Bioactive Disaccharide Associated with Autoimmune Disorders. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5316

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

Chicago Manual of Style (16th Edition):

Fermaintt, Charles Steven. “TREX1 C-Terminus Regulates Oligosaccharyltransfererase to Prevent the Accumulation of an Endogenous Bioactive Disaccharide Associated with Autoimmune Disorders.” 2018. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/5316.

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

MLA Handbook (7th Edition):

Fermaintt, Charles Steven. “TREX1 C-Terminus Regulates Oligosaccharyltransfererase to Prevent the Accumulation of an Endogenous Bioactive Disaccharide Associated with Autoimmune Disorders.” 2018. Web. 09 Jul 2020.

Vancouver:

Fermaintt CS. TREX1 C-Terminus Regulates Oligosaccharyltransfererase to Prevent the Accumulation of an Endogenous Bioactive Disaccharide Associated with Autoimmune Disorders. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2018. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/5316.

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

Council of Science Editors:

Fermaintt CS. TREX1 C-Terminus Regulates Oligosaccharyltransfererase to Prevent the Accumulation of an Endogenous Bioactive Disaccharide Associated with Autoimmune Disorders. [Thesis]. University of Texas Southwestern Medical Center; 2018. Available from: http://hdl.handle.net/2152.5/5316

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


University of Texas Southwestern Medical Center

4. Pham, Nam Dinh. Metabolic Pathways for Natural and Unnatural Sialic Acids.

Degree: 2014, University of Texas Southwestern Medical Center

 Carbohydrates, along with lipids, nucleic acids, and amino acids constitute the four main building blocks of life. This thesis will focus on sialic acid, a… (more)

Subjects/Keywords: N-Acetylneuraminic Acid; Polysaccharides; Sialic Acids; Sialyltransferases

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

APA (6th Edition):

Pham, N. D. (2014). Metabolic Pathways for Natural and Unnatural Sialic Acids. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5287

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

Chicago Manual of Style (16th Edition):

Pham, Nam Dinh. “Metabolic Pathways for Natural and Unnatural Sialic Acids.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/5287.

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

MLA Handbook (7th Edition):

Pham, Nam Dinh. “Metabolic Pathways for Natural and Unnatural Sialic Acids.” 2014. Web. 09 Jul 2020.

Vancouver:

Pham ND. Metabolic Pathways for Natural and Unnatural Sialic Acids. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/5287.

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

Council of Science Editors:

Pham ND. Metabolic Pathways for Natural and Unnatural Sialic Acids. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/5287

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


University of Texas Southwestern Medical Center

5. Shi, Lei. Metabolic Regulation of Quiescence Entry and Exit in Saccharomyces cerevisiae.

Degree: 2014, University of Texas Southwestern Medical Center

 Unicellular microorganisms often enter a state called quiescence when they encounter harsh environmental conditions. They stop growth and proliferation until conditions improve. In quiescence, the… (more)

Subjects/Keywords: Acetyl Coenzyme A; Cell Cycle; Cyclins; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Transcription, Genetic

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APA (6th Edition):

Shi, L. (2014). Metabolic Regulation of Quiescence Entry and Exit in Saccharomyces cerevisiae. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3955

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

Chicago Manual of Style (16th Edition):

Shi, Lei. “Metabolic Regulation of Quiescence Entry and Exit in Saccharomyces cerevisiae.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/3955.

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

MLA Handbook (7th Edition):

Shi, Lei. “Metabolic Regulation of Quiescence Entry and Exit in Saccharomyces cerevisiae.” 2014. Web. 09 Jul 2020.

Vancouver:

Shi L. Metabolic Regulation of Quiescence Entry and Exit in Saccharomyces cerevisiae. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/3955.

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

Council of Science Editors:

Shi L. Metabolic Regulation of Quiescence Entry and Exit in Saccharomyces cerevisiae. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3955

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


University of Texas Southwestern Medical Center

6. Parker, Randy B. Development of Chemical Tools to Discover and Characterize Sialic Acid Mediated Interactions.

Degree: 2014, University of Texas Southwestern Medical Center

 Glycosylation refers to the addition of carbohydrates onto proteins, lipids, and other biomolecules. Proteins and lipids on the cell surface are frequently found to be… (more)

Subjects/Keywords: Glycosylation; Neuraminidase; Polysaccharides; Sialic Acids

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APA (6th Edition):

Parker, R. B. (2014). Development of Chemical Tools to Discover and Characterize Sialic Acid Mediated Interactions. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3322

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

Chicago Manual of Style (16th Edition):

Parker, Randy B. “Development of Chemical Tools to Discover and Characterize Sialic Acid Mediated Interactions.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/3322.

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

MLA Handbook (7th Edition):

Parker, Randy B. “Development of Chemical Tools to Discover and Characterize Sialic Acid Mediated Interactions.” 2014. Web. 09 Jul 2020.

Vancouver:

Parker RB. Development of Chemical Tools to Discover and Characterize Sialic Acid Mediated Interactions. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/3322.

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

Council of Science Editors:

Parker RB. Development of Chemical Tools to Discover and Characterize Sialic Acid Mediated Interactions. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3322

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


University of Texas Southwestern Medical Center

7. Leija, Christopher Luis. Identification and Characterization of Drug Targets in the Pyrimidine and Purine Pathways of Trypanosoma brucei.

Degree: 2016, University of Texas Southwestern Medical Center

 The single-celled extracellular parasite Trypanosoma brucei causes Human African Trypanosomiasis (HAT), which is fatal if untreated. Current therapies result in severe side effects and require… (more)

Subjects/Keywords: Purines; Pyrimidines; Thymidine Kinase; Trypanosoma brucei brucei; Trypanosomiasis, African

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APA (6th Edition):

Leija, C. L. (2016). Identification and Characterization of Drug Targets in the Pyrimidine and Purine Pathways of Trypanosoma brucei. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6145

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

Chicago Manual of Style (16th Edition):

Leija, Christopher Luis. “Identification and Characterization of Drug Targets in the Pyrimidine and Purine Pathways of Trypanosoma brucei.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/6145.

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

MLA Handbook (7th Edition):

Leija, Christopher Luis. “Identification and Characterization of Drug Targets in the Pyrimidine and Purine Pathways of Trypanosoma brucei.” 2016. Web. 09 Jul 2020.

Vancouver:

Leija CL. Identification and Characterization of Drug Targets in the Pyrimidine and Purine Pathways of Trypanosoma brucei. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/6145.

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

Council of Science Editors:

Leija CL. Identification and Characterization of Drug Targets in the Pyrimidine and Purine Pathways of Trypanosoma brucei. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/6145

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


University of Texas Southwestern Medical Center

8. Cupka, Dorothy Lynn. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.

Degree: 2015, University of Texas Southwestern Medical Center

 Targeted delivery of imaging and therapeutic agents to tumors improves detection, characterization, and treatment of many types of cancers. Peptides are capable of efficient and… (more)

Subjects/Keywords: Antigens, Neoplasm; Integrins; Neoplasms; Peptides

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APA (6th Edition):

Cupka, D. L. (2015). Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4208

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

Chicago Manual of Style (16th Edition):

Cupka, Dorothy Lynn. “Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed July 09, 2020. http://hdl.handle.net/2152.5/4208.

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

MLA Handbook (7th Edition):

Cupka, Dorothy Lynn. “Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution.” 2015. Web. 09 Jul 2020.

Vancouver:

Cupka DL. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Jul 09]. Available from: http://hdl.handle.net/2152.5/4208.

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

Council of Science Editors:

Cupka DL. Development of an αᵥβ₆-Binding Peptide for In Vivo Applications: Modulation of Serum Stability and Biodistribution. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4208

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

.