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You searched for +publisher:"University of Texas Southwestern Medical Center" +contributor:("Mangelsdorf, David J."). Showing records 1 – 23 of 23 total matches.

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University of Texas Southwestern Medical Center

1. Schmidt, Daniel R. Bile Acids and Nuclear Receptors: Their Roles in Nutrition and Cancer.

Degree: 2012, University of Texas Southwestern Medical Center

 The bile acid receptor, also known as farnesoid X receptor (FXR), is essential for feedback regulation of bile acid synthesis. Bile acids are required for… (more)

Subjects/Keywords: Bile Acids and Salts; Vitamin A; Vitamin D

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APA (6th Edition):

Schmidt, D. R. (2012). Bile Acids and Nuclear Receptors: Their Roles in Nutrition and Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1114

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):

Schmidt, Daniel R. “Bile Acids and Nuclear Receptors: Their Roles in Nutrition and Cancer.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/1114.

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

MLA Handbook (7th Edition):

Schmidt, Daniel R. “Bile Acids and Nuclear Receptors: Their Roles in Nutrition and Cancer.” 2012. Web. 09 Aug 2020.

Vancouver:

Schmidt DR. Bile Acids and Nuclear Receptors: Their Roles in Nutrition and Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/1114.

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

Council of Science Editors:

Schmidt DR. Bile Acids and Nuclear Receptors: Their Roles in Nutrition and Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1114

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. Bookout, Angie Lynn. The Liver-Derived Endocrine Hormone FGF21 Alters Metabolism and Diurnal Behavior via the Nervous System.

Degree: 2012, University of Texas Southwestern Medical Center

 Fuel acquisition is essential to survival. During privation, the body protects glucose concentrations acutely by glycogenolysis, and later by gluconeogenesis and ketogenesis. Additionally, animals alter… (more)

Subjects/Keywords: Fibroblast Growth Factor; PPAR gamma; Liver

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APA (6th Edition):

Bookout, A. L. (2012). The Liver-Derived Endocrine Hormone FGF21 Alters Metabolism and Diurnal Behavior via the Nervous System. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/987

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):

Bookout, Angie Lynn. “The Liver-Derived Endocrine Hormone FGF21 Alters Metabolism and Diurnal Behavior via the Nervous System.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/987.

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

MLA Handbook (7th Edition):

Bookout, Angie Lynn. “The Liver-Derived Endocrine Hormone FGF21 Alters Metabolism and Diurnal Behavior via the Nervous System.” 2012. Web. 09 Aug 2020.

Vancouver:

Bookout AL. The Liver-Derived Endocrine Hormone FGF21 Alters Metabolism and Diurnal Behavior via the Nervous System. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/987.

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

Council of Science Editors:

Bookout AL. The Liver-Derived Endocrine Hormone FGF21 Alters Metabolism and Diurnal Behavior via the Nervous System. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/987

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. Wang, Zhu. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.

Degree: 2011, University of Texas Southwestern Medical Center

 The nuclear receptor DAF-12 plays a central role in controlling the larval development of C. elegans. Activation of DAF-12 by its ligands called dafachronic acids… (more)

Subjects/Keywords: Receptors, Cytoplasmic and Nuclear; Growth and Development; Caenorhabditis elegans Proteins

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APA (6th Edition):

Wang, Z. (2011). Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/855

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, Zhu. “Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/855.

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

MLA Handbook (7th Edition):

Wang, Zhu. “Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm.” 2011. Web. 09 Aug 2020.

Vancouver:

Wang Z. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/855.

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

Council of Science Editors:

Wang Z. Nuclear Receptor Controls Nematode Metabolism And Development: Insight Into Man’s Nemesis, the Conqueror Worm. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/855

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. Li, Tingting. Role of TGR5 in Bile Acid Metabolism.

Degree: 2011, University of Texas Southwestern Medical Center

 TGR5 is a G protein-coupled bile acid receptor present in various tissues in the body. Its agonism increases energy expenditure and lowers blood glucose. Thus,… (more)

Subjects/Keywords: Receptors, G-Protein-Coupled; Gallbladder; Metabolism

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APA (6th Edition):

Li, T. (2011). Role of TGR5 in Bile Acid Metabolism. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/869

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):

Li, Tingting. “Role of TGR5 in Bile Acid Metabolism.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/869.

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

MLA Handbook (7th Edition):

Li, Tingting. “Role of TGR5 in Bile Acid Metabolism.” 2011. Web. 09 Aug 2020.

Vancouver:

Li T. Role of TGR5 in Bile Acid Metabolism. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/869.

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

Council of Science Editors:

Li T. Role of TGR5 in Bile Acid Metabolism. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/869

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. Kir, Serkan. Regulation of Liver Metabolism by Fibroblast Growth Factor 19.

Degree: 2012, University of Texas Southwestern Medical Center

 Fibroblast Growth Factor (FGF) 19 is a postprandial enterokine up-regulated by bile acid receptor FXR upon bile acid uptake into the ileum. FGF19 inhibits hepatic… (more)

Subjects/Keywords: Liver Glycogen; Fibroblast Growth Factor; Protein Biosynthesis

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APA (6th Edition):

Kir, S. (2012). Regulation of Liver Metabolism by Fibroblast Growth Factor 19. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1027

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):

Kir, Serkan. “Regulation of Liver Metabolism by Fibroblast Growth Factor 19.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/1027.

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

MLA Handbook (7th Edition):

Kir, Serkan. “Regulation of Liver Metabolism by Fibroblast Growth Factor 19.” 2012. Web. 09 Aug 2020.

Vancouver:

Kir S. Regulation of Liver Metabolism by Fibroblast Growth Factor 19. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/1027.

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

Council of Science Editors:

Kir S. Regulation of Liver Metabolism by Fibroblast Growth Factor 19. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1027

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. 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 (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 August 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 Aug 2020.

Vancouver:

Pham ND. Metabolic Pathways for Natural and Unnatural Sialic Acids. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Aug 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

7. Stubblefield, Jeremy Joseph. Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics.

Degree: 2016, University of Texas Southwestern Medical Center

Pages 32-126 are incorrectly numbered as pages 31-125.

Cyclic processes in both behavior and physiology are aligned to the external environment through the circadian clock.… (more)

Subjects/Keywords: Circadian Rhythm; Nuclear Proteins; Poly A; Transcription Factors

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APA (6th Edition):

Stubblefield, J. J. (2016). Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5738

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):

Stubblefield, Jeremy Joseph. “Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/5738.

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

MLA Handbook (7th Edition):

Stubblefield, Jeremy Joseph. “Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics.” 2016. Web. 09 Aug 2020.

Vancouver:

Stubblefield JJ. Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/5738.

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

Council of Science Editors:

Stubblefield JJ. Nocturnin Regulates Metabolic Flux Through Maintenance of Poly(A) Tail Length Dynamics. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5738

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. Ryu, Keun Woo. Metabolic Regulation of Transcription Through Compartmentalized NAD+ Biosynthesis.

Degree: 2017, University of Texas Southwestern Medical Center

 Extracellular signaling and nutrient availability are major factors for the cell fate decision. Responds to extracellular information requires metabolic alterations and differential gene expression. Recently… (more)

Subjects/Keywords: Adipocytes; Adipogenesis; NAD; Nicotinamide-Nucleotide Adenylyltransferase; Transcription, Genetic

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APA (6th Edition):

Ryu, K. W. (2017). Metabolic Regulation of Transcription Through Compartmentalized NAD+ Biosynthesis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7742

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):

Ryu, Keun Woo. “Metabolic Regulation of Transcription Through Compartmentalized NAD+ Biosynthesis.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/7742.

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

MLA Handbook (7th Edition):

Ryu, Keun Woo. “Metabolic Regulation of Transcription Through Compartmentalized NAD+ Biosynthesis.” 2017. Web. 09 Aug 2020.

Vancouver:

Ryu KW. Metabolic Regulation of Transcription Through Compartmentalized NAD+ Biosynthesis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/7742.

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

Council of Science Editors:

Ryu KW. Metabolic Regulation of Transcription Through Compartmentalized NAD+ Biosynthesis. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7742

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. Udit, Swalpa 1985-. Naᵥ1.8+ Visceral Afferent Neurons: Roles in Metabolism and Inflammation.

Degree: 2013, University of Texas Southwestern Medical Center

 The increasing prevalence of obesity and its related comorbidities are major health issues facing western societies. Obesity involves a long-term, chronic perturbation of energy balance,… (more)

Subjects/Keywords: Afferent Pathways; Neurons, Afferent; Sodium Channels; Vagus Nerve

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APA (6th Edition):

Udit, S. 1. (2013). Naᵥ1.8+ Visceral Afferent Neurons: Roles in Metabolism and Inflammation. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3329

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):

Udit, Swalpa 1985-. “Naᵥ1.8+ Visceral Afferent Neurons: Roles in Metabolism and Inflammation.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/3329.

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

MLA Handbook (7th Edition):

Udit, Swalpa 1985-. “Naᵥ1.8+ Visceral Afferent Neurons: Roles in Metabolism and Inflammation.” 2013. Web. 09 Aug 2020.

Vancouver:

Udit S1. Naᵥ1.8+ Visceral Afferent Neurons: Roles in Metabolism and Inflammation. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/3329.

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

Council of Science Editors:

Udit S1. Naᵥ1.8+ Visceral Afferent Neurons: Roles in Metabolism and Inflammation. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/3329

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. Archer, Eric Jeffry. Engineered E. Coli That Detect and Respond to Gut Inflammation Through Nitric Oxide Sensing.

Degree: 2014, University of Texas Southwestern Medical Center

 Within the last several years, advances in synthetic biology have allowed for the development of re-programmed microorganisms that perform useful tasks in areas like fuel… (more)

Subjects/Keywords: Escherichia coli; Gastrointestinal Tract; Inflammation; Nitric Oxide

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APA (6th Edition):

Archer, E. J. (2014). Engineered E. Coli That Detect and Respond to Gut Inflammation Through Nitric Oxide Sensing. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3596

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):

Archer, Eric Jeffry. “Engineered E. Coli That Detect and Respond to Gut Inflammation Through Nitric Oxide Sensing.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/3596.

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

MLA Handbook (7th Edition):

Archer, Eric Jeffry. “Engineered E. Coli That Detect and Respond to Gut Inflammation Through Nitric Oxide Sensing.” 2014. Web. 09 Aug 2020.

Vancouver:

Archer EJ. Engineered E. Coli That Detect and Respond to Gut Inflammation Through Nitric Oxide Sensing. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/3596.

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

Council of Science Editors:

Archer EJ. Engineered E. Coli That Detect and Respond to Gut Inflammation Through Nitric Oxide Sensing. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3596

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. Schaffer, Nathaniel Elliot. DAF-12: A Novel Drug Target in Parasitic Nematodes.

Degree: 2014, University of Texas Southwestern Medical Center

 The nuclear receptor DAF-12, first identified in C. elegans, controls nematode species' entry into and exit from metabolically hypoactive resting states. In all of the… (more)

Subjects/Keywords: Antinematodal Agents; Drug Delivery Systems; Helminth Proteins; Nematoda; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Schaffer, N. E. (2014). DAF-12: A Novel Drug Target in Parasitic Nematodes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6590

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):

Schaffer, Nathaniel Elliot. “DAF-12: A Novel Drug Target in Parasitic Nematodes.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/6590.

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

MLA Handbook (7th Edition):

Schaffer, Nathaniel Elliot. “DAF-12: A Novel Drug Target in Parasitic Nematodes.” 2014. Web. 09 Aug 2020.

Vancouver:

Schaffer NE. DAF-12: A Novel Drug Target in Parasitic Nematodes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/6590.

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

Council of Science Editors:

Schaffer NE. DAF-12: A Novel Drug Target in Parasitic Nematodes. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/6590

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. Carstens, Ryan Murray. Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer.

Degree: 2015, University of Texas Southwestern Medical Center

 Nuclear hormone receptors are master regulators of diverse cellular functions implicated in tumor pathogenesis and as oncogenic drivers of many human cancers. To better understand… (more)

Subjects/Keywords: Carcinoma, Non-Small-Cell Lung; Receptors, Cytoplasmic and Nuclear; RNA, Small Interfering

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APA (6th Edition):

Carstens, R. M. (2015). Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4115

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):

Carstens, Ryan Murray. “Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/4115.

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

MLA Handbook (7th Edition):

Carstens, Ryan Murray. “Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer.” 2015. Web. 09 Aug 2020.

Vancouver:

Carstens RM. Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/4115.

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

Council of Science Editors:

Carstens RM. Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4115

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. Hicks, Jessica Anne. Human GW182 Paralogs Are the Central Organizers for RNA-Mediate Control of Transcription.

Degree: 2017, University of Texas Southwestern Medical Center

 RNA interference (RNAi) is an endogenous mechanism for regulating gene expression that can be manipulated for experimental or therapeutic purposes to knockdown protein expression. In… (more)

Subjects/Keywords: Argonaute Proteins; Autoantigens; Cell Nucleus; RNA Interference; RNA-Binding Proteins

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APA (6th Edition):

Hicks, J. A. (2017). Human GW182 Paralogs Are the Central Organizers for RNA-Mediate Control of Transcription. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4229

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):

Hicks, Jessica Anne. “Human GW182 Paralogs Are the Central Organizers for RNA-Mediate Control of Transcription.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/4229.

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

MLA Handbook (7th Edition):

Hicks, Jessica Anne. “Human GW182 Paralogs Are the Central Organizers for RNA-Mediate Control of Transcription.” 2017. Web. 09 Aug 2020.

Vancouver:

Hicks JA. Human GW182 Paralogs Are the Central Organizers for RNA-Mediate Control of Transcription. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/4229.

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

Council of Science Editors:

Hicks JA. Human GW182 Paralogs Are the Central Organizers for RNA-Mediate Control of Transcription. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/4229

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. Sondhi, Varun. The Search for the Endogenous RORg Ligand and Investigating the Role of Cytochrome B5 in Steroidogenesis and Regulation of the Cyp17a1 Lyase Reaction.

Degree: 2013, University of Texas Southwestern Medical Center

 RORg is an orphan nuclear receptor important in the regulation of immune development and function. RORg regulated TH17 cells have been implicated in the pathology… (more)

Subjects/Keywords: Cytochromes b5; Leydig Cells; Steroid 17-alpha-Hydroxylase

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APA (6th Edition):

Sondhi, V. (2013). The Search for the Endogenous RORg Ligand and Investigating the Role of Cytochrome B5 in Steroidogenesis and Regulation of the Cyp17a1 Lyase Reaction. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4104

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):

Sondhi, Varun. “The Search for the Endogenous RORg Ligand and Investigating the Role of Cytochrome B5 in Steroidogenesis and Regulation of the Cyp17a1 Lyase Reaction.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/4104.

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

MLA Handbook (7th Edition):

Sondhi, Varun. “The Search for the Endogenous RORg Ligand and Investigating the Role of Cytochrome B5 in Steroidogenesis and Regulation of the Cyp17a1 Lyase Reaction.” 2013. Web. 09 Aug 2020.

Vancouver:

Sondhi V. The Search for the Endogenous RORg Ligand and Investigating the Role of Cytochrome B5 in Steroidogenesis and Regulation of the Cyp17a1 Lyase Reaction. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/4104.

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

Council of Science Editors:

Sondhi V. The Search for the Endogenous RORg Ligand and Investigating the Role of Cytochrome B5 in Steroidogenesis and Regulation of the Cyp17a1 Lyase Reaction. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/4104

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. Atkin, Stan Dean. Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function.

Degree: 2014, University of Texas Southwestern Medical Center

 The timing of ovulation in mammals is set by a complex hypothalamic pituitary neuroendocrine axis. Kisspeptin neurons in the arcuate nucleus (Arc) are thought to… (more)

Subjects/Keywords: Kisspeptins; Neuropeptides; Receptors, Cytoplasmic and Nuclear; Reproduction

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APA (6th Edition):

Atkin, S. D. (2014). Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1425

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):

Atkin, Stan Dean. “Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/1425.

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

MLA Handbook (7th Edition):

Atkin, Stan Dean. “Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function.” 2014. Web. 09 Aug 2020.

Vancouver:

Atkin SD. Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/1425.

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

Council of Science Editors:

Atkin SD. Liver Receptor Homolog-1 Regulates Kisspeptin Expression in the Arcuate Nucleus to Promote Reproductive Axis Function. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/1425

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. 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 August 09, 2020. 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. 09 Aug 2020.

Vancouver:

Wang T. Understanding RNA Regulation Through Analysis of CLIP-Seq Data. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Aug 09]. 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

17. Zeve, Daniel. The Response of White Adipose Progenitor Cells to Physiological and Genetic Changes.

Degree: 2013, University of Texas Southwestern Medical Center

 We are in the midst of a dire, unprecedented and global epidemic of obesity and secondary sequelae, most prominently diabetes and hyperlipidemia. Underlying this epidemic… (more)

Subjects/Keywords: Adipocytes; Hyperlipidemias; Stem Cell Niche

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APA (6th Edition):

Zeve, D. (2013). The Response of White Adipose Progenitor Cells to Physiological and Genetic Changes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1358

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):

Zeve, Daniel. “The Response of White Adipose Progenitor Cells to Physiological and Genetic Changes.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/1358.

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

MLA Handbook (7th Edition):

Zeve, Daniel. “The Response of White Adipose Progenitor Cells to Physiological and Genetic Changes.” 2013. Web. 09 Aug 2020.

Vancouver:

Zeve D. The Response of White Adipose Progenitor Cells to Physiological and Genetic Changes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/1358.

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

Council of Science Editors:

Zeve D. The Response of White Adipose Progenitor Cells to Physiological and Genetic Changes. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1358

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

18. Zhi, Xiaoyong. Studies of Bile Acid-Like Signaling Pathways in Mammals and Nematodes.

Degree: 2010, University of Texas Southwestern Medical Center

 Bile acids are not only detergents for lipid solubilization and absorption, but also important signaling molecules. They regulate biological events in mammals by acting on… (more)

Subjects/Keywords: Bile Acids and Salts; Receptors, Cytoplasmic and Nuclear; Homeostasis

…Publication No. ________________ XIAOYONG ZHI The University of Texas Southwestern Medical Center at… 

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APA (6th Edition):

Zhi, X. (2010). Studies of Bile Acid-Like Signaling Pathways in Mammals and Nematodes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/919

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):

Zhi, Xiaoyong. “Studies of Bile Acid-Like Signaling Pathways in Mammals and Nematodes.” 2010. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/919.

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

MLA Handbook (7th Edition):

Zhi, Xiaoyong. “Studies of Bile Acid-Like Signaling Pathways in Mammals and Nematodes.” 2010. Web. 09 Aug 2020.

Vancouver:

Zhi X. Studies of Bile Acid-Like Signaling Pathways in Mammals and Nematodes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2010. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/919.

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

Council of Science Editors:

Zhi X. Studies of Bile Acid-Like Signaling Pathways in Mammals and Nematodes. [Thesis]. University of Texas Southwestern Medical Center; 2010. Available from: http://hdl.handle.net/2152.5/919

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. Sun, Tingwan. MicroRNAs: Tissue Expression and Role in 3T3-L1 Pre-Adipocyte Differentiation.

Degree: 2009, University of Texas Southwestern Medical Center

 MicroRNAs, which are endogenous small RNAs around 22 nucleotides, play important roles in many physiological processes. We investigated whether microRNAs regulate 3T3-L1 pre-adipocyte differentiation. The… (more)

Subjects/Keywords: MicroRNAs; Adipogenesis; HMGA2 Protein

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APA (6th Edition):

Sun, T. (2009). MicroRNAs: Tissue Expression and Role in 3T3-L1 Pre-Adipocyte Differentiation. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/399

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):

Sun, Tingwan. “MicroRNAs: Tissue Expression and Role in 3T3-L1 Pre-Adipocyte Differentiation.” 2009. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/399.

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

MLA Handbook (7th Edition):

Sun, Tingwan. “MicroRNAs: Tissue Expression and Role in 3T3-L1 Pre-Adipocyte Differentiation.” 2009. Web. 09 Aug 2020.

Vancouver:

Sun T. MicroRNAs: Tissue Expression and Role in 3T3-L1 Pre-Adipocyte Differentiation. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2009. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/399.

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

Council of Science Editors:

Sun T. MicroRNAs: Tissue Expression and Role in 3T3-L1 Pre-Adipocyte Differentiation. [Thesis]. University of Texas Southwestern Medical Center; 2009. Available from: http://hdl.handle.net/2152.5/399

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. Motola, Daniel Lewis. Identification of Ligands for the Orphan Nuclear Receptor DAF-12 That Govern Dauer Formation and Reproduction in C. Elegans.

Degree: 2006, University of Texas Southwestern Medical Center

 The orphan nuclear hormone receptor, DAF-12, plays a central role in the physiology of free-living nematode, C. elegans. DAF-12 is best known for its role… (more)

Subjects/Keywords: Ketosteroids; Caenorhabditis elegans Proteins; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Motola, D. L. (2006). Identification of Ligands for the Orphan Nuclear Receptor DAF-12 That Govern Dauer Formation and Reproduction in C. Elegans. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/726

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):

Motola, Daniel Lewis. “Identification of Ligands for the Orphan Nuclear Receptor DAF-12 That Govern Dauer Formation and Reproduction in C. Elegans.” 2006. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/726.

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

MLA Handbook (7th Edition):

Motola, Daniel Lewis. “Identification of Ligands for the Orphan Nuclear Receptor DAF-12 That Govern Dauer Formation and Reproduction in C. Elegans.” 2006. Web. 09 Aug 2020.

Vancouver:

Motola DL. Identification of Ligands for the Orphan Nuclear Receptor DAF-12 That Govern Dauer Formation and Reproduction in C. Elegans. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2006. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/726.

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

Council of Science Editors:

Motola DL. Identification of Ligands for the Orphan Nuclear Receptor DAF-12 That Govern Dauer Formation and Reproduction in C. Elegans. [Thesis]. University of Texas Southwestern Medical Center; 2006. Available from: http://hdl.handle.net/2152.5/726

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. Valdez, Melissa Renee. Myogenic BHLH Transcription Factors: Their Overlapping Functions and Direct Regulation of MEF2C Provide a Regulatory Network for the Maintenance and Amplification of Vertebrate Myogenesis.

Degree: 2003, University of Texas Southwestern Medical Center

 The myogenic basic helix-loop-helix (bHLH) genes - Myf5, MyoD, myogenin and MRF4 - exhibit distinct, but overlapping expression patterns during vertebrate myogenesis. Loss-of-function mutations in… (more)

Subjects/Keywords: Muscle Development; Myogenic Regulatory Factors; Basic Helix-Loop-Helix Transcription Factors

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APA (6th Edition):

Valdez, M. R. (2003). Myogenic BHLH Transcription Factors: Their Overlapping Functions and Direct Regulation of MEF2C Provide a Regulatory Network for the Maintenance and Amplification of Vertebrate Myogenesis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/488

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):

Valdez, Melissa Renee. “Myogenic BHLH Transcription Factors: Their Overlapping Functions and Direct Regulation of MEF2C Provide a Regulatory Network for the Maintenance and Amplification of Vertebrate Myogenesis.” 2003. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/488.

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

MLA Handbook (7th Edition):

Valdez, Melissa Renee. “Myogenic BHLH Transcription Factors: Their Overlapping Functions and Direct Regulation of MEF2C Provide a Regulatory Network for the Maintenance and Amplification of Vertebrate Myogenesis.” 2003. Web. 09 Aug 2020.

Vancouver:

Valdez MR. Myogenic BHLH Transcription Factors: Their Overlapping Functions and Direct Regulation of MEF2C Provide a Regulatory Network for the Maintenance and Amplification of Vertebrate Myogenesis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2003. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/488.

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

Council of Science Editors:

Valdez MR. Myogenic BHLH Transcription Factors: Their Overlapping Functions and Direct Regulation of MEF2C Provide a Regulatory Network for the Maintenance and Amplification of Vertebrate Myogenesis. [Thesis]. University of Texas Southwestern Medical Center; 2003. Available from: http://hdl.handle.net/2152.5/488

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. Jeong, Yangsik. Nuclear Receptors in Lung Cancer.

Degree: 2007, University of Texas Southwestern Medical Center

 Lung Cancer is a fatal disease with new diagnoses of more than 150,000 Americans every year. Although it has a relatively well-known etiology (e.g. smoking)… (more)

Subjects/Keywords: Gene Expression Regulation, Developmental; Embryonic Stem Cells; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Jeong, Y. (2007). Nuclear Receptors in Lung Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/280

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):

Jeong, Yangsik. “Nuclear Receptors in Lung Cancer.” 2007. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/280.

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

MLA Handbook (7th Edition):

Jeong, Yangsik. “Nuclear Receptors in Lung Cancer.” 2007. Web. 09 Aug 2020.

Vancouver:

Jeong Y. Nuclear Receptors in Lung Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2007. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/280.

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

Council of Science Editors:

Jeong Y. Nuclear Receptors in Lung Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2007. Available from: http://hdl.handle.net/2152.5/280

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. Valasek, Mark Andrew. The Regulation of Cholesterol Absorption: Nuclear Hormone Receptors and Niemann-Pick C1 Like 1.

Degree: 2007, University of Texas Southwestern Medical Center

 Cholesterol plays fundamental roles in cellular physiology, but it is also involved in many pathophysiological processes including atherosclerosis, cholelithiasis, and some forms of neurodegenerative disease.… (more)

Subjects/Keywords: Membrane Transport Proteins; Hypolipidemic Agents; Cholesterol

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APA (6th Edition):

Valasek, M. A. (2007). The Regulation of Cholesterol Absorption: Nuclear Hormone Receptors and Niemann-Pick C1 Like 1. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/664

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):

Valasek, Mark Andrew. “The Regulation of Cholesterol Absorption: Nuclear Hormone Receptors and Niemann-Pick C1 Like 1.” 2007. Thesis, University of Texas Southwestern Medical Center. Accessed August 09, 2020. http://hdl.handle.net/2152.5/664.

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

MLA Handbook (7th Edition):

Valasek, Mark Andrew. “The Regulation of Cholesterol Absorption: Nuclear Hormone Receptors and Niemann-Pick C1 Like 1.” 2007. Web. 09 Aug 2020.

Vancouver:

Valasek MA. The Regulation of Cholesterol Absorption: Nuclear Hormone Receptors and Niemann-Pick C1 Like 1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2007. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2152.5/664.

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

Council of Science Editors:

Valasek MA. The Regulation of Cholesterol Absorption: Nuclear Hormone Receptors and Niemann-Pick C1 Like 1. [Thesis]. University of Texas Southwestern Medical Center; 2007. Available from: http://hdl.handle.net/2152.5/664

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

.