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You searched for publisher:("University of Texas Southwestern Medical Center"). Showing records 1 – 30 of 1331 total matches.

[1] [2] [3] [4] [5] … [45]

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University of Texas Southwestern Medical Center

1. Ramesh, Sangheetha. Dissecting the Molecular Basis of the Antiphospholipid Syndrome.

Degree: 2011, University of Texas Southwestern Medical Center

 The antiphospholipid syndrome (APS) is an autoimmune disorder characterized by circulating antiphospholipid antibodies (aPL), thrombotic events, recurrent pregnancy loss, and increased risk of coronary artery… (more)

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APA (6th Edition):

Ramesh, S. (2011). Dissecting the Molecular Basis of the Antiphospholipid Syndrome. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/830

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):

Ramesh, Sangheetha. “Dissecting the Molecular Basis of the Antiphospholipid Syndrome.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/830.

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

MLA Handbook (7th Edition):

Ramesh, Sangheetha. “Dissecting the Molecular Basis of the Antiphospholipid Syndrome.” 2011. Web. 20 May 2019.

Vancouver:

Ramesh S. Dissecting the Molecular Basis of the Antiphospholipid Syndrome. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/830.

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

Council of Science Editors:

Ramesh S. Dissecting the Molecular Basis of the Antiphospholipid Syndrome. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/830

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. Braud, Jacquelyn Ashley. Neural Dysfunction during Decision-Making as a Predictor of Cocaine Relapse.

Degree: 2013, University of Texas Southwestern Medical Center

 Cocaine dependence is a costly disorder characterized by recurrent relapse events. The current investigation used functional magnetic resonance imaging (fMRI) during a decision-making task to… (more)

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APA (6th Edition):

Braud, J. A. (2013). Neural Dysfunction during Decision-Making as a Predictor of Cocaine Relapse. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1231

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):

Braud, Jacquelyn Ashley. “Neural Dysfunction during Decision-Making as a Predictor of Cocaine Relapse.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/1231.

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

MLA Handbook (7th Edition):

Braud, Jacquelyn Ashley. “Neural Dysfunction during Decision-Making as a Predictor of Cocaine Relapse.” 2013. Web. 20 May 2019.

Vancouver:

Braud JA. Neural Dysfunction during Decision-Making as a Predictor of Cocaine Relapse. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/1231.

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

Council of Science Editors:

Braud JA. Neural Dysfunction during Decision-Making as a Predictor of Cocaine Relapse. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1231

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. Montgomery, James. Creation of an Instructional Animation Showing the Development of the Human Placenta from Implantation to Term.

Degree: 2012, University of Texas Southwestern Medical Center

 This project was created to fill a need in available placental development instructional tools. In the current literature, there are few three-dimensional representations of placental… (more)

Subjects/Keywords: Placenta; Education, Medical; Students, Medical

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APA (6th Edition):

Montgomery, J. (2012). Creation of an Instructional Animation Showing the Development of the Human Placenta from Implantation to Term. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1355

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):

Montgomery, James. “Creation of an Instructional Animation Showing the Development of the Human Placenta from Implantation to Term.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/1355.

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

MLA Handbook (7th Edition):

Montgomery, James. “Creation of an Instructional Animation Showing the Development of the Human Placenta from Implantation to Term.” 2012. Web. 20 May 2019.

Vancouver:

Montgomery J. Creation of an Instructional Animation Showing the Development of the Human Placenta from Implantation to Term. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/1355.

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

Council of Science Editors:

Montgomery J. Creation of an Instructional Animation Showing the Development of the Human Placenta from Implantation to Term. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1355

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. Pineda, Carlos Tyler. The Cancer Specific Ubiquitin Ligase MAGE-A3/6-TRIM28 Drives Tumorigenesis by Ubiquitination and Proteasomal Degradation of AMPK.

Degree: 2015, University of Texas Southwestern Medical Center

 The genes MAGE-A3 and MAGE-A6 (MAGE-A3/6) have a unique expression pattern in which they are normally expressed in the adult testis but are aberrantly expressed… (more)

Subjects/Keywords: AMP-Activated Protein Kinases; Antigens, Neoplasm; Neoplasm Proteins; Neoplasms; Ubiquitination; Ubiquitin-Protein Ligases

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APA (6th Edition):

Pineda, C. T. (2015). The Cancer Specific Ubiquitin Ligase MAGE-A3/6-TRIM28 Drives Tumorigenesis by Ubiquitination and Proteasomal Degradation of AMPK. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4447

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):

Pineda, Carlos Tyler. “The Cancer Specific Ubiquitin Ligase MAGE-A3/6-TRIM28 Drives Tumorigenesis by Ubiquitination and Proteasomal Degradation of AMPK.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4447.

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

MLA Handbook (7th Edition):

Pineda, Carlos Tyler. “The Cancer Specific Ubiquitin Ligase MAGE-A3/6-TRIM28 Drives Tumorigenesis by Ubiquitination and Proteasomal Degradation of AMPK.” 2015. Web. 20 May 2019.

Vancouver:

Pineda CT. The Cancer Specific Ubiquitin Ligase MAGE-A3/6-TRIM28 Drives Tumorigenesis by Ubiquitination and Proteasomal Degradation of AMPK. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4447.

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

Council of Science Editors:

Pineda CT. The Cancer Specific Ubiquitin Ligase MAGE-A3/6-TRIM28 Drives Tumorigenesis by Ubiquitination and Proteasomal Degradation of AMPK. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4447

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. Ramirez, Michael Edward. The Emergence of Diverse Drug-Resistance Mechanisms from Drug Tolerant Cancer Persister Cells.

Degree: 2015, University of Texas Southwestern Medical Center

 Cancer therapy has traditionally focused on eliminating fast-growing populations of cells, yet a growing body of evidence suggests that small subpopulations of cancer cells can… (more)

Subjects/Keywords: Antineoplastic Agents; Drug Resistance, Neoplasm; Erlotinib Hydrochloride; Lung Neoplasms

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APA (6th Edition):

Ramirez, M. E. (2015). The Emergence of Diverse Drug-Resistance Mechanisms from Drug Tolerant Cancer Persister Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4448

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):

Ramirez, Michael Edward. “The Emergence of Diverse Drug-Resistance Mechanisms from Drug Tolerant Cancer Persister Cells.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4448.

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

MLA Handbook (7th Edition):

Ramirez, Michael Edward. “The Emergence of Diverse Drug-Resistance Mechanisms from Drug Tolerant Cancer Persister Cells.” 2015. Web. 20 May 2019.

Vancouver:

Ramirez ME. The Emergence of Diverse Drug-Resistance Mechanisms from Drug Tolerant Cancer Persister Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4448.

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

Council of Science Editors:

Ramirez ME. The Emergence of Diverse Drug-Resistance Mechanisms from Drug Tolerant Cancer Persister Cells. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4448

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. 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 (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 May 20, 2019. 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. 20 May 2019.

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 2019 May 20]. 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

7. Peyer, James Gregory. Refining Our Understanding of the Hematopoietic Stem Cell Niche.

Degree: 2015, University of Texas Southwestern Medical Center

 A major therapeutic goal of studying blood-forming hematopoietic stem cells (HSCs) is to understand the mechanisms by which HSCs are maintained in the bone marrow,… (more)

Subjects/Keywords: Bone Marrow Cells; Bone Marrow Transplantation; Hematopoietic Stem Cells; Stem Cell Niche

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APA (6th Edition):

Peyer, J. G. (2015). Refining Our Understanding of the Hematopoietic Stem Cell Niche. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4450

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):

Peyer, James Gregory. “Refining Our Understanding of the Hematopoietic Stem Cell Niche.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4450.

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

MLA Handbook (7th Edition):

Peyer, James Gregory. “Refining Our Understanding of the Hematopoietic Stem Cell Niche.” 2015. Web. 20 May 2019.

Vancouver:

Peyer JG. Refining Our Understanding of the Hematopoietic Stem Cell Niche. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4450.

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

Council of Science Editors:

Peyer JG. Refining Our Understanding of the Hematopoietic Stem Cell Niche. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4450

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. Chen, Pei-Hsuan. Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells.

Degree: 2015, University of Texas Southwestern Medical Center

 Cancer cells display oncogene-driven rewiring of metabolism to produce energy and macromolecules for growth. Inhibition of growth-promoting metabolic pathways may prove to be a useful… (more)

Subjects/Keywords: Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Lung Neoplasms

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APA (6th Edition):

Chen, P. (2015). Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4451

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):

Chen, Pei-Hsuan. “Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4451.

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

MLA Handbook (7th Edition):

Chen, Pei-Hsuan. “Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells.” 2015. Web. 20 May 2019.

Vancouver:

Chen P. Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4451.

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

Council of Science Editors:

Chen P. Metabolic Diversity in Human Non-Small Cell Lung Cancer Cells. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4451

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

9. Luethy, Lauren Nicole. Neuronal Dissemination Patterns of Three Distinct Viruses and Mechanisms Regulating Viral Retrograde Axonal Transport.

Degree: 2015, University of Texas Southwestern Medical Center

 Viruses from several distinct families can infect the central nervous system (CNS), but mechanisms and host factors that influence dissemination are not completely understood. I… (more)

Subjects/Keywords: Central Nervous System; Orthoreovirus, Mammalian; Peripheral Nerves; Poliovirus; Yellow fever virus

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APA (6th Edition):

Luethy, L. N. (2015). Neuronal Dissemination Patterns of Three Distinct Viruses and Mechanisms Regulating Viral Retrograde Axonal Transport. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4452

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):

Luethy, Lauren Nicole. “Neuronal Dissemination Patterns of Three Distinct Viruses and Mechanisms Regulating Viral Retrograde Axonal Transport.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4452.

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

MLA Handbook (7th Edition):

Luethy, Lauren Nicole. “Neuronal Dissemination Patterns of Three Distinct Viruses and Mechanisms Regulating Viral Retrograde Axonal Transport.” 2015. Web. 20 May 2019.

Vancouver:

Luethy LN. Neuronal Dissemination Patterns of Three Distinct Viruses and Mechanisms Regulating Viral Retrograde Axonal Transport. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4452.

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

Council of Science Editors:

Luethy LN. Neuronal Dissemination Patterns of Three Distinct Viruses and Mechanisms Regulating Viral Retrograde Axonal Transport. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4452

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

10. Zhang, Fang. A Synthetic Quorum Sensing System Reveals Interaction Between Extracellular Matrix and Quorum Sensing Molecules.

Degree: 2015, University of Texas Southwestern Medical Center

 Even though bacteria are unicellular organisms, they commonly reside in structured communities known as biofilms. One of the defining characteristics of biofilms is the presence… (more)

Subjects/Keywords: Bacillus subtilis; Biofilms; Quorum Sensing

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APA (6th Edition):

Zhang, F. (2015). A Synthetic Quorum Sensing System Reveals Interaction Between Extracellular Matrix and Quorum Sensing Molecules. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4453

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):

Zhang, Fang. “A Synthetic Quorum Sensing System Reveals Interaction Between Extracellular Matrix and Quorum Sensing Molecules.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4453.

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

MLA Handbook (7th Edition):

Zhang, Fang. “A Synthetic Quorum Sensing System Reveals Interaction Between Extracellular Matrix and Quorum Sensing Molecules.” 2015. Web. 20 May 2019.

Vancouver:

Zhang F. A Synthetic Quorum Sensing System Reveals Interaction Between Extracellular Matrix and Quorum Sensing Molecules. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4453.

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

Council of Science Editors:

Zhang F. A Synthetic Quorum Sensing System Reveals Interaction Between Extracellular Matrix and Quorum Sensing Molecules. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4453

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

11. Marty Santos, Leilani Marie. Elucidating the Role of Cellular Architecture in the Developing Pancreas.

Degree: 2015, University of Texas Southwestern Medical Center

 Many studies have focused on examining the intrinsic factors such as transcriptional regulators that instruct the step-wise acquisition of β-cell fate in the developing pancreas,… (more)

Subjects/Keywords: Cadherins; Cell Differentiation; Homeodomain Proteins; Pancreas; Trans-Activators

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APA (6th Edition):

Marty Santos, L. M. (2015). Elucidating the Role of Cellular Architecture in the Developing Pancreas. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4454

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):

Marty Santos, Leilani Marie. “Elucidating the Role of Cellular Architecture in the Developing Pancreas.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4454.

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

MLA Handbook (7th Edition):

Marty Santos, Leilani Marie. “Elucidating the Role of Cellular Architecture in the Developing Pancreas.” 2015. Web. 20 May 2019.

Vancouver:

Marty Santos LM. Elucidating the Role of Cellular Architecture in the Developing Pancreas. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4454.

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

Council of Science Editors:

Marty Santos LM. Elucidating the Role of Cellular Architecture in the Developing Pancreas. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4454

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

12. Lee, Ching En. Ceramide-Induced Alternative Translocation of TM4SF20.

Degree: 2015, University of Texas Southwestern Medical Center

 The polytopic membrane protein TM4SF20 (transmembrane 4 L6 family 20) is a protein containing four transmembrane helices that inhibits the Regulated Intramembrane Proteolysis (RIP) of… (more)

Subjects/Keywords: Ceramides; Cyclic AMP Response Element-Binding Protein; Endoplasmic Reticulum; Intracellular Membranes; Nerve Tissue Proteins; Tetraspanins

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APA (6th Edition):

Lee, C. E. (2015). Ceramide-Induced Alternative Translocation of TM4SF20. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4455

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):

Lee, Ching En. “Ceramide-Induced Alternative Translocation of TM4SF20.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4455.

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

MLA Handbook (7th Edition):

Lee, Ching En. “Ceramide-Induced Alternative Translocation of TM4SF20.” 2015. Web. 20 May 2019.

Vancouver:

Lee CE. Ceramide-Induced Alternative Translocation of TM4SF20. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4455.

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

Council of Science Editors:

Lee CE. Ceramide-Induced Alternative Translocation of TM4SF20. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4455

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

13. Jia, Luying. The Multifunctional Kinase Bub1 Acts as a Signaling Hub for the Spindle Checkpoint.

Degree: 2015, University of Texas Southwestern Medical Center

 The spindle checkpoint is an essential mechanism to ensure accurate chromosome segregation during mitosis. The checkpoint signal originates from the kinetochore, which is a huge… (more)

Subjects/Keywords: Anaphase-Promoting Complex-Cyclosome; Cdc20 Proteins; Cell Cycle Proteins; M Phase Cell Cycle Checkpoints; Protein-Serine-Threonine Kinases; Proto-Oncogene Proteins

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APA (6th Edition):

Jia, L. (2015). The Multifunctional Kinase Bub1 Acts as a Signaling Hub for the Spindle Checkpoint. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4456

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):

Jia, Luying. “The Multifunctional Kinase Bub1 Acts as a Signaling Hub for the Spindle Checkpoint.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4456.

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

MLA Handbook (7th Edition):

Jia, Luying. “The Multifunctional Kinase Bub1 Acts as a Signaling Hub for the Spindle Checkpoint.” 2015. Web. 20 May 2019.

Vancouver:

Jia L. The Multifunctional Kinase Bub1 Acts as a Signaling Hub for the Spindle Checkpoint. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4456.

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

Council of Science Editors:

Jia L. The Multifunctional Kinase Bub1 Acts as a Signaling Hub for the Spindle Checkpoint. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4456

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

14. Wang, Tao. Understanding RNA Regulation Through Analysis of CLIP-Seq Data.

Degree: 2015, University of Texas Southwestern Medical Center

 The past decades have witnessed a surge of discoveries revealing RNA regulation as a central player in cellular processes. The advent of cross-linking immunoprecipitation coupled… (more)

Subjects/Keywords: Genomics; High-Throughput Nucleotide Sequencing; RNA; RNA-Binding Proteins; Sequence Analysis, RNA

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APA (6th Edition):

Wang, T. (2015). Understanding RNA Regulation Through Analysis of CLIP-Seq Data. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4457

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):

Wang, Tao. “Understanding RNA Regulation Through Analysis of CLIP-Seq Data.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4457.

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

MLA Handbook (7th Edition):

Wang, Tao. “Understanding RNA Regulation Through Analysis of CLIP-Seq Data.” 2015. Web. 20 May 2019.

Vancouver:

Wang T. Understanding RNA Regulation Through Analysis of CLIP-Seq Data. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4457.

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

Council of Science Editors:

Wang T. Understanding RNA Regulation Through Analysis of CLIP-Seq Data. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4457

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

15. Tong, Jing. Improving Profile Similarity Search and Alignment of Protein Sequences.

Degree: 2015, University of Texas Southwestern Medical Center

 Protein function prediction is one of the most important problems in the field of computational biology. The most reliable method to predict protein function is… (more)

Subjects/Keywords: Protein Conformation; Proteins; Proteomics; Sequence Alignment; Sequence Homology

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APA (6th Edition):

Tong, J. (2015). Improving Profile Similarity Search and Alignment of Protein Sequences. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4458

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):

Tong, Jing. “Improving Profile Similarity Search and Alignment of Protein Sequences.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4458.

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

MLA Handbook (7th Edition):

Tong, Jing. “Improving Profile Similarity Search and Alignment of Protein Sequences.” 2015. Web. 20 May 2019.

Vancouver:

Tong J. Improving Profile Similarity Search and Alignment of Protein Sequences. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4458.

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

Council of Science Editors:

Tong J. Improving Profile Similarity Search and Alignment of Protein Sequences. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4458

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

16. Dalvi, Maithili Prafulla. Targeting Taxane-Platin Resistant Non-Small Cell Lung Cancers with Jumonji C Histone Lysine Demethylase Inhibitors.

Degree: 2015, University of Texas Southwestern Medical Center

 Taxane-platin doublet therapy provides benefit as front-line chemotherapy in advanced and localized non-small cell lung cancer (NSCLC); however the majority of patients relapse with drug… (more)

Subjects/Keywords: Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Drug Resistance, Neoplasm; Jumonji Domain-Containing Histone Demethylases; Taxoids

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APA (6th Edition):

Dalvi, M. P. (2015). Targeting Taxane-Platin Resistant Non-Small Cell Lung Cancers with Jumonji C Histone Lysine Demethylase Inhibitors. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4459

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):

Dalvi, Maithili Prafulla. “Targeting Taxane-Platin Resistant Non-Small Cell Lung Cancers with Jumonji C Histone Lysine Demethylase Inhibitors.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4459.

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

MLA Handbook (7th Edition):

Dalvi, Maithili Prafulla. “Targeting Taxane-Platin Resistant Non-Small Cell Lung Cancers with Jumonji C Histone Lysine Demethylase Inhibitors.” 2015. Web. 20 May 2019.

Vancouver:

Dalvi MP. Targeting Taxane-Platin Resistant Non-Small Cell Lung Cancers with Jumonji C Histone Lysine Demethylase Inhibitors. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4459.

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

Council of Science Editors:

Dalvi MP. Targeting Taxane-Platin Resistant Non-Small Cell Lung Cancers with Jumonji C Histone Lysine Demethylase Inhibitors. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4459

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

17. Adebesin, Adeniyi Michael. Studies Toward the Syntheses of Antiarrythmic, Anti-Virulence, and Anticancer Small Molecules.

Degree: 2015, University of Texas Southwestern Medical Center

 This work is comprised of three projects: a) the development of antiarrythmic analogs of 17(R),18(S)-epoxyeicosatetraenoic acid for the treatment of atrial fibrillation, b) the development… (more)

Subjects/Keywords: Anti-Bacterial Agents; Gram-Negative Bacteria; Protein Kinase Inhibitors; Protein Kinases; Quorum Sensing; Sulfonamides

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APA (6th Edition):

Adebesin, A. M. (2015). Studies Toward the Syntheses of Antiarrythmic, Anti-Virulence, and Anticancer Small Molecules. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4460

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):

Adebesin, Adeniyi Michael. “Studies Toward the Syntheses of Antiarrythmic, Anti-Virulence, and Anticancer Small Molecules.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4460.

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

MLA Handbook (7th Edition):

Adebesin, Adeniyi Michael. “Studies Toward the Syntheses of Antiarrythmic, Anti-Virulence, and Anticancer Small Molecules.” 2015. Web. 20 May 2019.

Vancouver:

Adebesin AM. Studies Toward the Syntheses of Antiarrythmic, Anti-Virulence, and Anticancer Small Molecules. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4460.

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

Council of Science Editors:

Adebesin AM. Studies Toward the Syntheses of Antiarrythmic, Anti-Virulence, and Anticancer Small Molecules. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4460

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

18. Wylie, Annika Dawn. P53 Genes Act to Restrain Mobile Elements.

Degree: 2015, University of Texas Southwestern Medical Center

 Oncogenic stress provokes tumor suppression by p53 but the extent to which this regulatory axis is conserved remains unknown. Using a biosensor to visualize p53… (more)

Subjects/Keywords: Genes, p53; Retroelements; Tumor Suppressor Protein p53

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APA (6th Edition):

Wylie, A. D. (2015). P53 Genes Act to Restrain Mobile Elements. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4461

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):

Wylie, Annika Dawn. “P53 Genes Act to Restrain Mobile Elements.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4461.

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

MLA Handbook (7th Edition):

Wylie, Annika Dawn. “P53 Genes Act to Restrain Mobile Elements.” 2015. Web. 20 May 2019.

Vancouver:

Wylie AD. P53 Genes Act to Restrain Mobile Elements. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4461.

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

Council of Science Editors:

Wylie AD. P53 Genes Act to Restrain Mobile Elements. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4461

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

19. Hight, Suzie K. An In Vivo Functional Genomics Screen Identifies New Regulators of Tumorigenesis in Non-Small Cell Lung Cancer.

Degree: 2015, University of Texas Southwestern Medical Center

 Cancer cells are characterized by the aberrant regulation of signaling pathways that govern responses to growth stimuli, resulting in dysregulated cellular proliferation. The accumulated genomic… (more)

Subjects/Keywords: Carcinoma, Non-Small-Cell Lung; Gene Expression Regulation, Neoplastic; Lung Neoplasms; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Hight, S. K. (2015). An In Vivo Functional Genomics Screen Identifies New Regulators of Tumorigenesis in Non-Small Cell Lung Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4462

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):

Hight, Suzie K. “An In Vivo Functional Genomics Screen Identifies New Regulators of Tumorigenesis in Non-Small Cell Lung Cancer.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4462.

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

MLA Handbook (7th Edition):

Hight, Suzie K. “An In Vivo Functional Genomics Screen Identifies New Regulators of Tumorigenesis in Non-Small Cell Lung Cancer.” 2015. Web. 20 May 2019.

Vancouver:

Hight SK. An In Vivo Functional Genomics Screen Identifies New Regulators of Tumorigenesis in Non-Small Cell Lung Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4462.

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

Council of Science Editors:

Hight SK. An In Vivo Functional Genomics Screen Identifies New Regulators of Tumorigenesis in Non-Small Cell Lung Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4462

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

20. Nagati, Jason Sharif. Dual Mechanisms Regulating Alpha Subunit-Specific Activity in Hypoxia-Inducible Factor Signaling.

Degree: 2015, University of Texas Southwestern Medical Center

 The ability to adapt to and protect from environmental stresses is essential to survival and has played a major role in fitness selection during evolution.… (more)

Subjects/Keywords: Acetates; Basic Helix-Loop-Helix Transcription Factors; Erythropoiesis; Signal Transduction; Stress, Physiological; Tumor Microenvironment

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APA (6th Edition):

Nagati, J. S. (2015). Dual Mechanisms Regulating Alpha Subunit-Specific Activity in Hypoxia-Inducible Factor Signaling. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4463

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):

Nagati, Jason Sharif. “Dual Mechanisms Regulating Alpha Subunit-Specific Activity in Hypoxia-Inducible Factor Signaling.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4463.

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

MLA Handbook (7th Edition):

Nagati, Jason Sharif. “Dual Mechanisms Regulating Alpha Subunit-Specific Activity in Hypoxia-Inducible Factor Signaling.” 2015. Web. 20 May 2019.

Vancouver:

Nagati JS. Dual Mechanisms Regulating Alpha Subunit-Specific Activity in Hypoxia-Inducible Factor Signaling. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4463.

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

Council of Science Editors:

Nagati JS. Dual Mechanisms Regulating Alpha Subunit-Specific Activity in Hypoxia-Inducible Factor Signaling. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4463

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

21. Gao, Daxing. Roles of Cyclic GMP-AMP Synthase in Immune Defense Against Retroviruses and Autoimmunity.

Degree: 2015, University of Texas Southwestern Medical Center

 The presence of DNA in the cytosol is known to trigger robust innate immunity. Cyclic GMP-AMP synthase (cGAS) is the sensor of cytosolic DNA and… (more)

Subjects/Keywords: Autoimmune Diseases; DNA; Nucleotidyltransferases

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APA (6th Edition):

Gao, D. (2015). Roles of Cyclic GMP-AMP Synthase in Immune Defense Against Retroviruses and Autoimmunity. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4465

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):

Gao, Daxing. “Roles of Cyclic GMP-AMP Synthase in Immune Defense Against Retroviruses and Autoimmunity.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4465.

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

MLA Handbook (7th Edition):

Gao, Daxing. “Roles of Cyclic GMP-AMP Synthase in Immune Defense Against Retroviruses and Autoimmunity.” 2015. Web. 20 May 2019.

Vancouver:

Gao D. Roles of Cyclic GMP-AMP Synthase in Immune Defense Against Retroviruses and Autoimmunity. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4465.

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

Council of Science Editors:

Gao D. Roles of Cyclic GMP-AMP Synthase in Immune Defense Against Retroviruses and Autoimmunity. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4465

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

22. Gonzalez, Dante Alan. EFA6/PSD3, Arf6 Modulator, Regulates Ethanol-Induced Behaviors Via the Insulin Receptor Signaling Pathway in Flies and Humans.

Degree: 2015, University of Texas Southwestern Medical Center

 Despite the tremendous hazard that alcohol (ethanol) poses to society world-wide, our progress on the molecular and physiological understanding of how ethanol use disorders (AUD)… (more)

Subjects/Keywords: Central Nervous System Depressants; Ethanol; Gene Expression Regulation; Ribosomal Protein S6 Kinases, 70-kDa

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APA (6th Edition):

Gonzalez, D. A. (2015). EFA6/PSD3, Arf6 Modulator, Regulates Ethanol-Induced Behaviors Via the Insulin Receptor Signaling Pathway in Flies and Humans. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4466

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):

Gonzalez, Dante Alan. “EFA6/PSD3, Arf6 Modulator, Regulates Ethanol-Induced Behaviors Via the Insulin Receptor Signaling Pathway in Flies and Humans.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/4466.

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

MLA Handbook (7th Edition):

Gonzalez, Dante Alan. “EFA6/PSD3, Arf6 Modulator, Regulates Ethanol-Induced Behaviors Via the Insulin Receptor Signaling Pathway in Flies and Humans.” 2015. Web. 20 May 2019.

Vancouver:

Gonzalez DA. EFA6/PSD3, Arf6 Modulator, Regulates Ethanol-Induced Behaviors Via the Insulin Receptor Signaling Pathway in Flies and Humans. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/4466.

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

Council of Science Editors:

Gonzalez DA. EFA6/PSD3, Arf6 Modulator, Regulates Ethanol-Induced Behaviors Via the Insulin Receptor Signaling Pathway in Flies and Humans. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4466

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

23. Bowen, Irene Masiulis. Regulation and Function of Apoer2 and Vidlr in the Central Nervous and Reproductive Systems.

Degree: 2009, University of Texas Southwestern Medical Center

 The LDL receptor gene family is an evolutionarily ancient family of membrane spanning proteins composed of a diverse collection of receptors that share common domains… (more)

Subjects/Keywords: LDL-Receptor Related Proteins; Selenium; Signal Transduction

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APA (6th Edition):

Bowen, I. M. (2009). Regulation and Function of Apoer2 and Vidlr in the Central Nervous and Reproductive Systems. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/242

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):

Bowen, Irene Masiulis. “Regulation and Function of Apoer2 and Vidlr in the Central Nervous and Reproductive Systems.” 2009. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/242.

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

MLA Handbook (7th Edition):

Bowen, Irene Masiulis. “Regulation and Function of Apoer2 and Vidlr in the Central Nervous and Reproductive Systems.” 2009. Web. 20 May 2019.

Vancouver:

Bowen IM. Regulation and Function of Apoer2 and Vidlr in the Central Nervous and Reproductive Systems. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2009. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/242.

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

Council of Science Editors:

Bowen IM. Regulation and Function of Apoer2 and Vidlr in the Central Nervous and Reproductive Systems. [Thesis]. University of Texas Southwestern Medical Center; 2009. Available from: http://hdl.handle.net/2152.5/242

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

24. Ocal, Ozhan. Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes.

Degree: 2012, University of Texas Southwestern Medical Center

 Diabetes mellitus is a collection of metabolic diseases with chronic hyperglycemia as their common syndrome. Type 1 diabetes results from pancreatic insulin producing beta cell… (more)

Subjects/Keywords: Diabetes Mellitus, Type 1; RGS Proteins; Receptors, G-Protein-Coupled

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APA (6th Edition):

Ocal, O. (2012). Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1034

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):

Ocal, Ozhan. “Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/1034.

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

MLA Handbook (7th Edition):

Ocal, Ozhan. “Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes.” 2012. Web. 20 May 2019.

Vancouver:

Ocal O. Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/1034.

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

Council of Science Editors:

Ocal O. Rgs16 is a Pancreatic Reporter of Chronic Hyperglycemia in Diabetes. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1034

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

25. Orme, Jacob Jennings. Molecular Players in Lupus: Leads from Proteomic Screens.

Degree: 2014, University of Texas Southwestern Medical Center

 Systemic Lupus Erythematosus is a multifactorial systemic autoimmune disorder marked by anti-nuclear antibodies (ANA), rashes and photosensitivity, joint inflammation, nephritis, and other clinical criteria. SLE… (more)

Subjects/Keywords: ADAM10 Protein; ADAM17 Protein; Lupus Erythematosus, Systemic; Proto-Oncogene Proteins; Receptor Protein-Tyrosine Kinases

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APA (6th Edition):

Orme, J. J. (2014). Molecular Players in Lupus: Leads from Proteomic Screens. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5282

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):

Orme, Jacob Jennings. “Molecular Players in Lupus: Leads from Proteomic Screens.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/5282.

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

MLA Handbook (7th Edition):

Orme, Jacob Jennings. “Molecular Players in Lupus: Leads from Proteomic Screens.” 2014. Web. 20 May 2019.

Vancouver:

Orme JJ. Molecular Players in Lupus: Leads from Proteomic Screens. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/5282.

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

Council of Science Editors:

Orme JJ. Molecular Players in Lupus: Leads from Proteomic Screens. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/5282

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

26. McFarlane, Matthew Ryan. Ghrelin: The Hunger Hormone that Isn't.

Degree: 2014, University of Texas Southwestern Medical Center

 Ghrelin is a 28-amino acid acylated peptide hormone secreted by endocrine cells in the stomach. It was first identified in 1999 and shortly thereafter shown… (more)

Subjects/Keywords: Appetite; Body Weight; Diet, High-Fat; Ghrelin

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APA (6th Edition):

McFarlane, M. R. (2014). Ghrelin: The Hunger Hormone that Isn't. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5283

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):

McFarlane, Matthew Ryan. “Ghrelin: The Hunger Hormone that Isn't.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/5283.

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

MLA Handbook (7th Edition):

McFarlane, Matthew Ryan. “Ghrelin: The Hunger Hormone that Isn't.” 2014. Web. 20 May 2019.

Vancouver:

McFarlane MR. Ghrelin: The Hunger Hormone that Isn't. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/5283.

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

Council of Science Editors:

McFarlane MR. Ghrelin: The Hunger Hormone that Isn't. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/5283

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

27. Nguyen, Suong Thu. Essentiality and Regulation of Deoxyhypusination in Trypanosoma brucei.

Degree: 2014, University of Texas Southwestern Medical Center

 Human African trypanosomiasis is caused by protozoan parasite Trypanosoma brucei. T. brucei and other trypanosomatids require spermidine for the formation of trypanothione, a unique thiol-redox… (more)

Subjects/Keywords: Lysine; Peptide Initiation Factors; Protein Processing, Post-Translational; Protozoan Proteins; RNA-Binding Proteins; Trypanosoma brucei brucei

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

APA (6th Edition):

Nguyen, S. T. (2014). Essentiality and Regulation of Deoxyhypusination in Trypanosoma brucei. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5284

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):

Nguyen, Suong Thu. “Essentiality and Regulation of Deoxyhypusination in Trypanosoma brucei.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/5284.

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

MLA Handbook (7th Edition):

Nguyen, Suong Thu. “Essentiality and Regulation of Deoxyhypusination in Trypanosoma brucei.” 2014. Web. 20 May 2019.

Vancouver:

Nguyen ST. Essentiality and Regulation of Deoxyhypusination in Trypanosoma brucei. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/5284.

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

Council of Science Editors:

Nguyen ST. Essentiality and Regulation of Deoxyhypusination in Trypanosoma brucei. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/5284

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

28. Cai, Xin. Functional Prions in Mammalian Innate Immune Signaling.

Degree: 2014, University of Texas Southwestern Medical Center

 Pathogens and cellular danger signals activate mammalian cytosolic sensors such as RIG-I and NLRP3 which signal through respective adaptor proteins MAVS and ASC to produce… (more)

Subjects/Keywords: Biological Evolution; Immunity, Innate; Inflammasomes; Prions; Signal Transduction; Yeasts

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

APA (6th Edition):

Cai, X. (2014). Functional Prions in Mammalian Innate Immune Signaling. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5285

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):

Cai, Xin. “Functional Prions in Mammalian Innate Immune Signaling.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/5285.

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

MLA Handbook (7th Edition):

Cai, Xin. “Functional Prions in Mammalian Innate Immune Signaling.” 2014. Web. 20 May 2019.

Vancouver:

Cai X. Functional Prions in Mammalian Innate Immune Signaling. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/5285.

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

Council of Science Editors:

Cai X. Functional Prions in Mammalian Innate Immune Signaling. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/5285

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

29. Rajagopalan, Kartik N. The Role of Pyruvate Dehydrogenase in Cell Growth.

Degree: 2014, University of Texas Southwestern Medical Center

 Otto Warburg's observation that tumor cells have increased rates of glucose uptake and lactate secretion in comparison to normal cells spawned his notion that tumors… (more)

Subjects/Keywords: Cell Proliferation; Fatty Acids; Glucose; Protein Kinases; Pyruvate Dehydrogenase Complex

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

APA (6th Edition):

Rajagopalan, K. N. (2014). The Role of Pyruvate Dehydrogenase in Cell Growth. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5286

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):

Rajagopalan, Kartik N. “The Role of Pyruvate Dehydrogenase in Cell Growth.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed May 20, 2019. http://hdl.handle.net/2152.5/5286.

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

MLA Handbook (7th Edition):

Rajagopalan, Kartik N. “The Role of Pyruvate Dehydrogenase in Cell Growth.” 2014. Web. 20 May 2019.

Vancouver:

Rajagopalan KN. The Role of Pyruvate Dehydrogenase in Cell Growth. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 May 20]. Available from: http://hdl.handle.net/2152.5/5286.

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

Council of Science Editors:

Rajagopalan KN. The Role of Pyruvate Dehydrogenase in Cell Growth. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/5286

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

30. 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 May 20, 2019. 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. 20 May 2019.

Vancouver:

Pham ND. Metabolic Pathways for Natural and Unnatural Sialic Acids. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 May 20]. 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

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