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You searched for +publisher:"Texas A&M University" +contributor:("Tian, Yanan"). Showing records 1 – 29 of 29 total matches.

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Texas A&M University

1. Wang, Meichen. Xenobiotic Receptor PXR-Mediated Resistance to Salmonella Invasion and Its Mechanism.

Degree: MS, Toxicology, 2016, Texas A&M University

 Pregnane X receptor (PXR) is a ligand-activated nuclear receptor that regulates gene expression of the metabolizing enzymes that are involved in detoxification of endogenous and… (more)

Subjects/Keywords: PXR; bacterial invasion

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APA (6th Edition):

Wang, M. (2016). Xenobiotic Receptor PXR-Mediated Resistance to Salmonella Invasion and Its Mechanism. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174243

Chicago Manual of Style (16th Edition):

Wang, Meichen. “Xenobiotic Receptor PXR-Mediated Resistance to Salmonella Invasion and Its Mechanism.” 2016. Masters Thesis, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/174243.

MLA Handbook (7th Edition):

Wang, Meichen. “Xenobiotic Receptor PXR-Mediated Resistance to Salmonella Invasion and Its Mechanism.” 2016. Web. 24 Oct 2020.

Vancouver:

Wang M. Xenobiotic Receptor PXR-Mediated Resistance to Salmonella Invasion and Its Mechanism. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/174243.

Council of Science Editors:

Wang M. Xenobiotic Receptor PXR-Mediated Resistance to Salmonella Invasion and Its Mechanism. [Masters Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/174243


Texas A&M University

2. Banerjee, Nivedita. Polyphenol-induced Anti-inflammatory and Cytotoxic Activities in Breast and Colon Cancer: Potential Role of miRNA's in Cell Survival and Inflammation.

Degree: PhD, Toxicology, 2013, Texas A&M University

 Cancer is a major cause of death worldwide. Hence, there is a great need to develop novel therapeutic agents for the prevention and treatment of… (more)

Subjects/Keywords: Polyphenol; Polyphenolics; Cancer; miRNA; cytotoxicity

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APA (6th Edition):

Banerjee, N. (2013). Polyphenol-induced Anti-inflammatory and Cytotoxic Activities in Breast and Colon Cancer: Potential Role of miRNA's in Cell Survival and Inflammation. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151661

Chicago Manual of Style (16th Edition):

Banerjee, Nivedita. “Polyphenol-induced Anti-inflammatory and Cytotoxic Activities in Breast and Colon Cancer: Potential Role of miRNA's in Cell Survival and Inflammation.” 2013. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/151661.

MLA Handbook (7th Edition):

Banerjee, Nivedita. “Polyphenol-induced Anti-inflammatory and Cytotoxic Activities in Breast and Colon Cancer: Potential Role of miRNA's in Cell Survival and Inflammation.” 2013. Web. 24 Oct 2020.

Vancouver:

Banerjee N. Polyphenol-induced Anti-inflammatory and Cytotoxic Activities in Breast and Colon Cancer: Potential Role of miRNA's in Cell Survival and Inflammation. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/151661.

Council of Science Editors:

Banerjee N. Polyphenol-induced Anti-inflammatory and Cytotoxic Activities in Breast and Colon Cancer: Potential Role of miRNA's in Cell Survival and Inflammation. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151661


Texas A&M University

3. Wu, Mingqi. Population SAMC, ChIP-chip Data Analysis and Beyond.

Degree: PhD, Statistics, 2011, Texas A&M University

 This dissertation research consists of two topics, population stochastics approximation Monte Carlo (Pop-SAMC) for Baysian model selection problems and ChIP-chip data analysis. The following two… (more)

Subjects/Keywords: Markov Chain Monte Carlo; Stochastic Approximation; Metropolis-Hastings Algorithm; Bayesian Model Selection; ChIP-chip; Latent Variable; Multiple Hypothesis Test

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APA (6th Edition):

Wu, M. (2011). Population SAMC, ChIP-chip Data Analysis and Beyond. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8752

Chicago Manual of Style (16th Edition):

Wu, Mingqi. “Population SAMC, ChIP-chip Data Analysis and Beyond.” 2011. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8752.

MLA Handbook (7th Edition):

Wu, Mingqi. “Population SAMC, ChIP-chip Data Analysis and Beyond.” 2011. Web. 24 Oct 2020.

Vancouver:

Wu M. Population SAMC, ChIP-chip Data Analysis and Beyond. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8752.

Council of Science Editors:

Wu M. Population SAMC, ChIP-chip Data Analysis and Beyond. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8752


Texas A&M University

4. Eagleton, Navada Lorraine. Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression.

Degree: MS, Toxicology, 2011, Texas A&M University

 To understand the mechanisms of transcriptional regulation of PXR, we performed yeast two-hybrid screenings to search for PXR-interacting proteins in a human liver cDNA library… (more)

Subjects/Keywords: pregnane X receptor; PXR; CNOT2; colon cancer

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APA (6th Edition):

Eagleton, N. L. (2011). Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029

Chicago Manual of Style (16th Edition):

Eagleton, Navada Lorraine. “Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression.” 2011. Masters Thesis, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029.

MLA Handbook (7th Edition):

Eagleton, Navada Lorraine. “Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression.” 2011. Web. 24 Oct 2020.

Vancouver:

Eagleton NL. Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression. [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029.

Council of Science Editors:

Eagleton NL. Novel Functions for the Pregnane X Receptor include Regulation of mRNA Turnover and Involvement in Colon Cancer Progression. [Masters Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8029


Texas A&M University

5. Francis Stuart, Samantha D. The Pro-Antioxidant Role of Zinc Supplementation in Cadmium-Treated Choroid Plexus.

Degree: MS, Toxicology, 2014, Texas A&M University

 Cadmium (Cd) is a toxic heavy metal with no known physiological function in higher order animals. Previous studies in primary cultures of neonatal rat choroid… (more)

Subjects/Keywords: choroid plexus; cadmium; zinc; oxidative stress; glutathione; metallothionein; heat-shock protein 70; hemeoxygenase

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APA (6th Edition):

Francis Stuart, S. D. (2014). The Pro-Antioxidant Role of Zinc Supplementation in Cadmium-Treated Choroid Plexus. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152822

Chicago Manual of Style (16th Edition):

Francis Stuart, Samantha D. “The Pro-Antioxidant Role of Zinc Supplementation in Cadmium-Treated Choroid Plexus.” 2014. Masters Thesis, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/152822.

MLA Handbook (7th Edition):

Francis Stuart, Samantha D. “The Pro-Antioxidant Role of Zinc Supplementation in Cadmium-Treated Choroid Plexus.” 2014. Web. 24 Oct 2020.

Vancouver:

Francis Stuart SD. The Pro-Antioxidant Role of Zinc Supplementation in Cadmium-Treated Choroid Plexus. [Internet] [Masters thesis]. Texas A&M University; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/152822.

Council of Science Editors:

Francis Stuart SD. The Pro-Antioxidant Role of Zinc Supplementation in Cadmium-Treated Choroid Plexus. [Masters Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152822


Texas A&M University

6. Yu, Xue. Exploring the Molecular Interactions Between Host Cells and Cryptosporidium parvum During Invasion.

Degree: PhD, Veterinary Pathobiology, 2018, Texas A&M University

 Cryptosporidium parvum is a zoonotic protozoan parasite belonging to the Phylum Apicomplexa and a causative agent of mild to severe watery diarrhea in humans and… (more)

Subjects/Keywords: Cryptosporidum parvum; invasion mechnisms; host cells

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APA (6th Edition):

Yu, X. (2018). Exploring the Molecular Interactions Between Host Cells and Cryptosporidium parvum During Invasion. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173901

Chicago Manual of Style (16th Edition):

Yu, Xue. “Exploring the Molecular Interactions Between Host Cells and Cryptosporidium parvum During Invasion.” 2018. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/173901.

MLA Handbook (7th Edition):

Yu, Xue. “Exploring the Molecular Interactions Between Host Cells and Cryptosporidium parvum During Invasion.” 2018. Web. 24 Oct 2020.

Vancouver:

Yu X. Exploring the Molecular Interactions Between Host Cells and Cryptosporidium parvum During Invasion. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/173901.

Council of Science Editors:

Yu X. Exploring the Molecular Interactions Between Host Cells and Cryptosporidium parvum During Invasion. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173901


Texas A&M University

7. Xie, Ying. Transcriptional Regulation of Pregnane X Receptor by Protein Arginine Methyltransferase.

Degree: PhD, Toxicology, 2011, Texas A&M University

 Pregnane X receptor (PXR) is a ligand-dependent transcription factor that plays an important role in xenobiotic/drug metabolism. The ligand-receptor interaction transcriptionally activates phase I and… (more)

Subjects/Keywords: PXR; PRMT1; epigenetics

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APA (6th Edition):

Xie, Y. (2011). Transcriptional Regulation of Pregnane X Receptor by Protein Arginine Methyltransferase. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7978

Chicago Manual of Style (16th Edition):

Xie, Ying. “Transcriptional Regulation of Pregnane X Receptor by Protein Arginine Methyltransferase.” 2011. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7978.

MLA Handbook (7th Edition):

Xie, Ying. “Transcriptional Regulation of Pregnane X Receptor by Protein Arginine Methyltransferase.” 2011. Web. 24 Oct 2020.

Vancouver:

Xie Y. Transcriptional Regulation of Pregnane X Receptor by Protein Arginine Methyltransferase. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7978.

Council of Science Editors:

Xie Y. Transcriptional Regulation of Pregnane X Receptor by Protein Arginine Methyltransferase. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7978


Texas A&M University

8. Garcia-Mazcorro, Jose. Evaluation of the Gastrointestinal Microbiota in Response to Dietary and Therapeutic Factors in Cats and Dogs Using Molecular Methods.

Degree: PhD, Biomedical Sciences, 2012, Texas A&M University

 The gastrointestinal (GI) tract of cats and dogs is inhabited by many different types of microorganisms, known as the GI microbiota. Mounting evidence suggests that… (more)

Subjects/Keywords: microbial; ecology; gastrointestinal; molecular; 16S rRNA gene

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APA (6th Edition):

Garcia-Mazcorro, J. (2012). Evaluation of the Gastrointestinal Microbiota in Response to Dietary and Therapeutic Factors in Cats and Dogs Using Molecular Methods. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10481

Chicago Manual of Style (16th Edition):

Garcia-Mazcorro, Jose. “Evaluation of the Gastrointestinal Microbiota in Response to Dietary and Therapeutic Factors in Cats and Dogs Using Molecular Methods.” 2012. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10481.

MLA Handbook (7th Edition):

Garcia-Mazcorro, Jose. “Evaluation of the Gastrointestinal Microbiota in Response to Dietary and Therapeutic Factors in Cats and Dogs Using Molecular Methods.” 2012. Web. 24 Oct 2020.

Vancouver:

Garcia-Mazcorro J. Evaluation of the Gastrointestinal Microbiota in Response to Dietary and Therapeutic Factors in Cats and Dogs Using Molecular Methods. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10481.

Council of Science Editors:

Garcia-Mazcorro J. Evaluation of the Gastrointestinal Microbiota in Response to Dietary and Therapeutic Factors in Cats and Dogs Using Molecular Methods. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10481


Texas A&M University

9. Robinson, Abraham. Development of a Biomarker and Clay Based Remediation Strategy for Populations at Risk for Fumonisin Toxicosis.

Degree: PhD, Toxicology, 2012, Texas A&M University

 Fumonisin B1 is the most prevalent congener of the fumonisin mycotoxins produced by Fusarium verticilliodies and is considered by many to be the most toxic.… (more)

Subjects/Keywords: Fumonisin; mycotoxin; FB1; Ghana; NovaSil; Enterosorbent

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APA (6th Edition):

Robinson, A. (2012). Development of a Biomarker and Clay Based Remediation Strategy for Populations at Risk for Fumonisin Toxicosis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8814

Chicago Manual of Style (16th Edition):

Robinson, Abraham. “Development of a Biomarker and Clay Based Remediation Strategy for Populations at Risk for Fumonisin Toxicosis.” 2012. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8814.

MLA Handbook (7th Edition):

Robinson, Abraham. “Development of a Biomarker and Clay Based Remediation Strategy for Populations at Risk for Fumonisin Toxicosis.” 2012. Web. 24 Oct 2020.

Vancouver:

Robinson A. Development of a Biomarker and Clay Based Remediation Strategy for Populations at Risk for Fumonisin Toxicosis. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8814.

Council of Science Editors:

Robinson A. Development of a Biomarker and Clay Based Remediation Strategy for Populations at Risk for Fumonisin Toxicosis. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8814


Texas A&M University

10. Hedrick, Erik Duane. Diindolylmethane Analogs as Novel NR4A1 Antagonists and as a Novel Class of Anticancer Agents and Sp Transcription Factors as Nononcogene Addiction Genes That Are Targets of ROS Inducing Agents.

Degree: PhD, Toxicology, 2016, Texas A&M University

 The orphan nuclear receptor 4A1 (NR4A1) and specificity protein (Sp) transcription factors (TFs) are both overexpressed in the majority of solid tumors. Our laboratory has… (more)

Subjects/Keywords: NR4A1; Sp transcription factors

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APA (6th Edition):

Hedrick, E. D. (2016). Diindolylmethane Analogs as Novel NR4A1 Antagonists and as a Novel Class of Anticancer Agents and Sp Transcription Factors as Nononcogene Addiction Genes That Are Targets of ROS Inducing Agents. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/159116

Chicago Manual of Style (16th Edition):

Hedrick, Erik Duane. “Diindolylmethane Analogs as Novel NR4A1 Antagonists and as a Novel Class of Anticancer Agents and Sp Transcription Factors as Nononcogene Addiction Genes That Are Targets of ROS Inducing Agents.” 2016. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/159116.

MLA Handbook (7th Edition):

Hedrick, Erik Duane. “Diindolylmethane Analogs as Novel NR4A1 Antagonists and as a Novel Class of Anticancer Agents and Sp Transcription Factors as Nononcogene Addiction Genes That Are Targets of ROS Inducing Agents.” 2016. Web. 24 Oct 2020.

Vancouver:

Hedrick ED. Diindolylmethane Analogs as Novel NR4A1 Antagonists and as a Novel Class of Anticancer Agents and Sp Transcription Factors as Nononcogene Addiction Genes That Are Targets of ROS Inducing Agents. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/159116.

Council of Science Editors:

Hedrick ED. Diindolylmethane Analogs as Novel NR4A1 Antagonists and as a Novel Class of Anticancer Agents and Sp Transcription Factors as Nononcogene Addiction Genes That Are Targets of ROS Inducing Agents. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/159116

11. Cheng, Yating. The Role of Long Noncoding RNAs in Cancer and Microbiota-derived Aryl Hydrocarbon Receptor Ligands.

Degree: PhD, Toxicology, 2016, Texas A&M University

 LncRNAs are a group of non-coding RNAs containing >200 nucleotides and these RNAs have no significant protein coding potential. In the past 10-15 years the… (more)

Subjects/Keywords: Long noncoding RNAs; Pancreatic cancer; Gut microbiota, AhR

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APA (6th Edition):

Cheng, Y. (2016). The Role of Long Noncoding RNAs in Cancer and Microbiota-derived Aryl Hydrocarbon Receptor Ligands. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/159030

Chicago Manual of Style (16th Edition):

Cheng, Yating. “The Role of Long Noncoding RNAs in Cancer and Microbiota-derived Aryl Hydrocarbon Receptor Ligands.” 2016. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/159030.

MLA Handbook (7th Edition):

Cheng, Yating. “The Role of Long Noncoding RNAs in Cancer and Microbiota-derived Aryl Hydrocarbon Receptor Ligands.” 2016. Web. 24 Oct 2020.

Vancouver:

Cheng Y. The Role of Long Noncoding RNAs in Cancer and Microbiota-derived Aryl Hydrocarbon Receptor Ligands. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/159030.

Council of Science Editors:

Cheng Y. The Role of Long Noncoding RNAs in Cancer and Microbiota-derived Aryl Hydrocarbon Receptor Ligands. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/159030


Texas A&M University

12. Ramachandran Nair Vasanthakum, Vijayalekshmi. Mechanisms of Action of Metformin as an Anti-cancer Agent.

Degree: PhD, Toxicology, 2014, Texas A&M University

 Cancer is the second leading cause of death worldwide and epidemiological studies suggest the association of diabetes mellitus with an enhanced risk for multiple cancers.… (more)

Subjects/Keywords: Specificity protein transcription factors; IGF-1R; EGFR; mTOR

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APA (6th Edition):

Ramachandran Nair Vasanthakum, V. (2014). Mechanisms of Action of Metformin as an Anti-cancer Agent. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153440

Chicago Manual of Style (16th Edition):

Ramachandran Nair Vasanthakum, Vijayalekshmi. “Mechanisms of Action of Metformin as an Anti-cancer Agent.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/153440.

MLA Handbook (7th Edition):

Ramachandran Nair Vasanthakum, Vijayalekshmi. “Mechanisms of Action of Metformin as an Anti-cancer Agent.” 2014. Web. 24 Oct 2020.

Vancouver:

Ramachandran Nair Vasanthakum V. Mechanisms of Action of Metformin as an Anti-cancer Agent. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/153440.

Council of Science Editors:

Ramachandran Nair Vasanthakum V. Mechanisms of Action of Metformin as an Anti-cancer Agent. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153440


Texas A&M University

13. Jia, Qian 1980-. n-3 PUFA and Curcumin Modulate the Resolution of Murine Intestinal Inflammtion.

Degree: PhD, Nutrition, 2011, Texas A&M University

 Bioactive food components containing n-3 polyunsaturated fatty acids (PUFA) and curcumin modulate multiple determinants that link inflammation to cancer initiation and progression. In this dissertation,… (more)

Subjects/Keywords: Resolution; Intestinal inflammation; Curcumin; n-3 PUFA

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APA (6th Edition):

Jia, Q. 1. (2011). n-3 PUFA and Curcumin Modulate the Resolution of Murine Intestinal Inflammtion. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/150942

Chicago Manual of Style (16th Edition):

Jia, Qian 1980-. “n-3 PUFA and Curcumin Modulate the Resolution of Murine Intestinal Inflammtion.” 2011. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/150942.

MLA Handbook (7th Edition):

Jia, Qian 1980-. “n-3 PUFA and Curcumin Modulate the Resolution of Murine Intestinal Inflammtion.” 2011. Web. 24 Oct 2020.

Vancouver:

Jia Q1. n-3 PUFA and Curcumin Modulate the Resolution of Murine Intestinal Inflammtion. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/150942.

Council of Science Editors:

Jia Q1. n-3 PUFA and Curcumin Modulate the Resolution of Murine Intestinal Inflammtion. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/150942


Texas A&M University

14. Sreevalsan, Sandeep. Molecular Mechanisms of Cannabinoids as Anti-cancer Agents.

Degree: PhD, Toxicology, 2013, Texas A&M University

 Cancer is a growing health concern world-wide and is the second most common cause of death after heart diseases. Current treatment strategies such as surgery,… (more)

Subjects/Keywords: Cancer; Cannabinoids

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APA (6th Edition):

Sreevalsan, S. (2013). Molecular Mechanisms of Cannabinoids as Anti-cancer Agents. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151011

Chicago Manual of Style (16th Edition):

Sreevalsan, Sandeep. “Molecular Mechanisms of Cannabinoids as Anti-cancer Agents.” 2013. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/151011.

MLA Handbook (7th Edition):

Sreevalsan, Sandeep. “Molecular Mechanisms of Cannabinoids as Anti-cancer Agents.” 2013. Web. 24 Oct 2020.

Vancouver:

Sreevalsan S. Molecular Mechanisms of Cannabinoids as Anti-cancer Agents. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/151011.

Council of Science Editors:

Sreevalsan S. Molecular Mechanisms of Cannabinoids as Anti-cancer Agents. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151011

15. Banerjee, Nivedita. Systematic Approach to Compare the Inflammatory Response of Liver Cell Culture Systems Exposed to Silver, Copper, and Nickel Nanoparticles.

Degree: MS, Toxicology, 2011, Texas A&M University

 Although nano-sized metal colloids are used in industrial and medicinal applications, little is known about the potential liver toxicity of these materials after occupational or… (more)

Subjects/Keywords: Nanoparticles; Inflammation; Cytokines; Cellular Uptake; Cytotoxicity; Co-culture

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APA (6th Edition):

Banerjee, N. (2011). Systematic Approach to Compare the Inflammatory Response of Liver Cell Culture Systems Exposed to Silver, Copper, and Nickel Nanoparticles. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8414

Chicago Manual of Style (16th Edition):

Banerjee, Nivedita. “Systematic Approach to Compare the Inflammatory Response of Liver Cell Culture Systems Exposed to Silver, Copper, and Nickel Nanoparticles.” 2011. Masters Thesis, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8414.

MLA Handbook (7th Edition):

Banerjee, Nivedita. “Systematic Approach to Compare the Inflammatory Response of Liver Cell Culture Systems Exposed to Silver, Copper, and Nickel Nanoparticles.” 2011. Web. 24 Oct 2020.

Vancouver:

Banerjee N. Systematic Approach to Compare the Inflammatory Response of Liver Cell Culture Systems Exposed to Silver, Copper, and Nickel Nanoparticles. [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8414.

Council of Science Editors:

Banerjee N. Systematic Approach to Compare the Inflammatory Response of Liver Cell Culture Systems Exposed to Silver, Copper, and Nickel Nanoparticles. [Masters Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8414

16. Guo, Fengguang. Long Chain Fatty Acyl-Coenzyme A Synthetase as Novel Drug Targets in Cryptosporidium parvum.

Degree: PhD, Veterinary Microbiology, 2014, Texas A&M University

 Cryptosporidium parvum infects both humans and animals, and continues to be a significant opportunistic pathogen among AIDS patients and one of the leading diarrheal pathogens… (more)

Subjects/Keywords: Cryptosporidium parvum; cryptosporidiosis; long-chain fatty acyl-CoA synthetase; drug target; triacsin C

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APA (6th Edition):

Guo, F. (2014). Long Chain Fatty Acyl-Coenzyme A Synthetase as Novel Drug Targets in Cryptosporidium parvum. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153424

Chicago Manual of Style (16th Edition):

Guo, Fengguang. “Long Chain Fatty Acyl-Coenzyme A Synthetase as Novel Drug Targets in Cryptosporidium parvum.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/153424.

MLA Handbook (7th Edition):

Guo, Fengguang. “Long Chain Fatty Acyl-Coenzyme A Synthetase as Novel Drug Targets in Cryptosporidium parvum.” 2014. Web. 24 Oct 2020.

Vancouver:

Guo F. Long Chain Fatty Acyl-Coenzyme A Synthetase as Novel Drug Targets in Cryptosporidium parvum. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/153424.

Council of Science Editors:

Guo F. Long Chain Fatty Acyl-Coenzyme A Synthetase as Novel Drug Targets in Cryptosporidium parvum. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153424

17. Eltahan, Rana Abbas Khedr. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.

Degree: PhD, Biomedical Sciences, 2018, Texas A&M University

 Cryptosporidium parvum is a water-borne and food-borne apicomplexan pathogen. It is one of the top four diarrheal-causing pathogens in children under the age of five… (more)

Subjects/Keywords: : Apicomplexan; Cryptosporidium parvum; Glucose-6-phosphate isomerase (GPI); Ebselen; Hexokinase (HK): Drug target

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APA (6th Edition):

Eltahan, R. A. K. (2018). Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173649

Chicago Manual of Style (16th Edition):

Eltahan, Rana Abbas Khedr. “Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.” 2018. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/173649.

MLA Handbook (7th Edition):

Eltahan, Rana Abbas Khedr. “Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.” 2018. Web. 24 Oct 2020.

Vancouver:

Eltahan RAK. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/173649.

Council of Science Editors:

Eltahan RAK. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173649

18. Wang, Gang. Effects of Genetic Variants on Gene Expression Variability.

Degree: PhD, Biomedical Sciences, 2016, Texas A&M University

 Variation and variability of gene expression are central concepts in biology. Variation refers to differences among individuals, whereas variability refers to the potential of a… (more)

Subjects/Keywords: aberrant gene expression; additive genetic effect; decanalization; epistasis; evQTL; expression variability; gene expression; genetic interaction; phenotypic variability; twin cohort.

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APA (6th Edition):

Wang, G. (2016). Effects of Genetic Variants on Gene Expression Variability. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/157059

Chicago Manual of Style (16th Edition):

Wang, Gang. “Effects of Genetic Variants on Gene Expression Variability.” 2016. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/157059.

MLA Handbook (7th Edition):

Wang, Gang. “Effects of Genetic Variants on Gene Expression Variability.” 2016. Web. 24 Oct 2020.

Vancouver:

Wang G. Effects of Genetic Variants on Gene Expression Variability. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/157059.

Council of Science Editors:

Wang G. Effects of Genetic Variants on Gene Expression Variability. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/157059

19. Fuentes, Natividad R. Plasma Membrane Lipid Therapy: Disruption of Oncogenic Ras Driven Phenotypes by Membrane Targeted Dietary Bioactives (Mtdb).

Degree: PhD, Toxicology, 2017, Texas A&M University

 Approximately 30-50% of colorectal cancers contain KRas mutations, which confer resistance to standard therapy. A diet high in long-chain n-3 polyunsaturated fatty acids (n-3 PUFA)… (more)

Subjects/Keywords: Cancer; Fish Oil; N-3 PUFA; DHA; EPA; Ras; Membrane

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APA (6th Edition):

Fuentes, N. R. (2017). Plasma Membrane Lipid Therapy: Disruption of Oncogenic Ras Driven Phenotypes by Membrane Targeted Dietary Bioactives (Mtdb). (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173219

Chicago Manual of Style (16th Edition):

Fuentes, Natividad R. “Plasma Membrane Lipid Therapy: Disruption of Oncogenic Ras Driven Phenotypes by Membrane Targeted Dietary Bioactives (Mtdb).” 2017. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/173219.

MLA Handbook (7th Edition):

Fuentes, Natividad R. “Plasma Membrane Lipid Therapy: Disruption of Oncogenic Ras Driven Phenotypes by Membrane Targeted Dietary Bioactives (Mtdb).” 2017. Web. 24 Oct 2020.

Vancouver:

Fuentes NR. Plasma Membrane Lipid Therapy: Disruption of Oncogenic Ras Driven Phenotypes by Membrane Targeted Dietary Bioactives (Mtdb). [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/173219.

Council of Science Editors:

Fuentes NR. Plasma Membrane Lipid Therapy: Disruption of Oncogenic Ras Driven Phenotypes by Membrane Targeted Dietary Bioactives (Mtdb). [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/173219

20. Pathi, Satya. Mechanisms of Action of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in Colon Cancer.

Degree: PhD, Toxicology, 2012, Texas A&M University

 Non-steroidal anti-inflammatory drugs (NSAIDs) and their NO derivatives (NO-NSAIDs), and synthetic analogs are highly effective as anticancer agents that exhibit relatively low toxicity compared to… (more)

Subjects/Keywords: Cancer; Colon cancer; NSAIDs; Specificity protein transcription factors; chemotherapy

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APA (6th Edition):

Pathi, S. (2012). Mechanisms of Action of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in Colon Cancer. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11608

Chicago Manual of Style (16th Edition):

Pathi, Satya. “Mechanisms of Action of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in Colon Cancer.” 2012. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11608.

MLA Handbook (7th Edition):

Pathi, Satya. “Mechanisms of Action of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in Colon Cancer.” 2012. Web. 24 Oct 2020.

Vancouver:

Pathi S. Mechanisms of Action of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in Colon Cancer. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11608.

Council of Science Editors:

Pathi S. Mechanisms of Action of Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) in Colon Cancer. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11608

21. Hu, Shengdi. Endogenous Synthesis of Glycine from Hydroxyproline in Neonatal Pigs.

Degree: PhD, Animal Science, 2017, Texas A&M University

 This study was conducted to test the hypothesis that hydroxyproline is a novel and major substrate for endogenous synthesis of glycine in sow-reared pigs. At… (more)

Subjects/Keywords: Glycine; Hydroxyproline; Piglets

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APA (6th Edition):

Hu, S. (2017). Endogenous Synthesis of Glycine from Hydroxyproline in Neonatal Pigs. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173105

Chicago Manual of Style (16th Edition):

Hu, Shengdi. “Endogenous Synthesis of Glycine from Hydroxyproline in Neonatal Pigs.” 2017. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/173105.

MLA Handbook (7th Edition):

Hu, Shengdi. “Endogenous Synthesis of Glycine from Hydroxyproline in Neonatal Pigs.” 2017. Web. 24 Oct 2020.

Vancouver:

Hu S. Endogenous Synthesis of Glycine from Hydroxyproline in Neonatal Pigs. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/173105.

Council of Science Editors:

Hu S. Endogenous Synthesis of Glycine from Hydroxyproline in Neonatal Pigs. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/173105

22. Kim, KyoungHyun. Domain analysis for estrogen receptor/Sp1-mediated transactivation and detection of estrogen receptor/Sp1 protein interactions in living cells.

Degree: PhD, Toxicology, 2005, Texas A&M University

 Estrogen Receptor ? (ER?)/Sp1 activation of GC-rich gene promoters in breast cancer cells is dependent, in part, on the activation function 1 (AF1) of ER?.… (more)

Subjects/Keywords: Estrogen receptor; Sp1; antiestrogens

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APA (6th Edition):

Kim, K. (2005). Domain analysis for estrogen receptor/Sp1-mediated transactivation and detection of estrogen receptor/Sp1 protein interactions in living cells. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/2666

Chicago Manual of Style (16th Edition):

Kim, KyoungHyun. “Domain analysis for estrogen receptor/Sp1-mediated transactivation and detection of estrogen receptor/Sp1 protein interactions in living cells.” 2005. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/2666.

MLA Handbook (7th Edition):

Kim, KyoungHyun. “Domain analysis for estrogen receptor/Sp1-mediated transactivation and detection of estrogen receptor/Sp1 protein interactions in living cells.” 2005. Web. 24 Oct 2020.

Vancouver:

Kim K. Domain analysis for estrogen receptor/Sp1-mediated transactivation and detection of estrogen receptor/Sp1 protein interactions in living cells. [Internet] [Doctoral dissertation]. Texas A&M University; 2005. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/2666.

Council of Science Editors:

Kim K. Domain analysis for estrogen receptor/Sp1-mediated transactivation and detection of estrogen receptor/Sp1 protein interactions in living cells. [Doctoral Dissertation]. Texas A&M University; 2005. Available from: http://hdl.handle.net/1969.1/2666

23. Naspinski, Christine S. Toxicity Analysis of Polycyclic Aromatic Hydrocarbon Mixtures.

Degree: PhD, Toxicology, 2010, Texas A&M University

 Polycyclic aromatic hydrocarbons (PAHs) are widely distributed in the environment and are generated by many sources. Though the potential of PAH-rich mixtures to cause health… (more)

Subjects/Keywords: PAH; PXR; Mus musculus; house dust; benzo[a]pyrene

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APA (6th Edition):

Naspinski, C. S. (2010). Toxicity Analysis of Polycyclic Aromatic Hydrocarbon Mixtures. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-310

Chicago Manual of Style (16th Edition):

Naspinski, Christine S. “Toxicity Analysis of Polycyclic Aromatic Hydrocarbon Mixtures.” 2010. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-310.

MLA Handbook (7th Edition):

Naspinski, Christine S. “Toxicity Analysis of Polycyclic Aromatic Hydrocarbon Mixtures.” 2010. Web. 24 Oct 2020.

Vancouver:

Naspinski CS. Toxicity Analysis of Polycyclic Aromatic Hydrocarbon Mixtures. [Internet] [Doctoral dissertation]. Texas A&M University; 2010. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-310.

Council of Science Editors:

Naspinski CS. Toxicity Analysis of Polycyclic Aromatic Hydrocarbon Mixtures. [Doctoral Dissertation]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-310


Texas A&M University

24. Fritzler, Jason Michael. Cryptosporidium parvum: enhancing our understanding of its unique fatty acid metabolism and the elucidation of putative new inhibitors.

Degree: PhD, Veterinary Microbiology, 2008, Texas A&M University

 Cryptosporidium parvum is widely known for outbreaks within the immunocompetent population, as well its sometimes excruciating effects as an opportunistic agent in AIDS patients. Our… (more)

Subjects/Keywords: Cryptosporidium parvum; polyketide synthase; fatty acid elongase; acyl-CoA binding protein; drug screen

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APA (6th Edition):

Fritzler, J. M. (2008). Cryptosporidium parvum: enhancing our understanding of its unique fatty acid metabolism and the elucidation of putative new inhibitors. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/85980

Chicago Manual of Style (16th Edition):

Fritzler, Jason Michael. “Cryptosporidium parvum: enhancing our understanding of its unique fatty acid metabolism and the elucidation of putative new inhibitors.” 2008. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/85980.

MLA Handbook (7th Edition):

Fritzler, Jason Michael. “Cryptosporidium parvum: enhancing our understanding of its unique fatty acid metabolism and the elucidation of putative new inhibitors.” 2008. Web. 24 Oct 2020.

Vancouver:

Fritzler JM. Cryptosporidium parvum: enhancing our understanding of its unique fatty acid metabolism and the elucidation of putative new inhibitors. [Internet] [Doctoral dissertation]. Texas A&M University; 2008. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/85980.

Council of Science Editors:

Fritzler JM. Cryptosporidium parvum: enhancing our understanding of its unique fatty acid metabolism and the elucidation of putative new inhibitors. [Doctoral Dissertation]. Texas A&M University; 2008. Available from: http://hdl.handle.net/1969.1/85980


Texas A&M University

25. Zeng, Bin. Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum.

Degree: PhD, Veterinary Microbiology, 2009, Texas A&M University

 From opportunistic protist Cryptosporidium parvum we identified and functionally assayed a fatty acyl-CoA-binding protein (ACBP) gene. The CpACBP1 gene encodes a protein of 268 aa… (more)

Subjects/Keywords: acyl-CoA binding protein; oxysterol binding protein-related proteins

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APA (6th Edition):

Zeng, B. (2009). Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1211

Chicago Manual of Style (16th Edition):

Zeng, Bin. “Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum.” 2009. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1211.

MLA Handbook (7th Edition):

Zeng, Bin. “Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum.” 2009. Web. 24 Oct 2020.

Vancouver:

Zeng B. Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1211.

Council of Science Editors:

Zeng B. Functional characterization of acyl-CoA binding protein (ACBP) and oxysterol binding protein-related proteins (ORPS) from Cryptosporidium parvum. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1211


Texas A&M University

26. Tress, Ursula. Maternal adrenocorticotropin, cortisol and thyroid hormone responses to chronic binge alcohol exposure throughout gestation: ovine model.

Degree: MS, Veterinary Physiology, 2009, Texas A&M University

 This study investigated the effect of chronic alcohol exposure on the responses of the maternal hypothalamus-pituitary adrenal axis (HPA-axis) and thyroid hormones throughout gestation using… (more)

Subjects/Keywords: fetal alcohol syndrome; prenatal; birth defects; ACTH; cortisol; thyroid hormones

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APA (6th Edition):

Tress, U. (2009). Maternal adrenocorticotropin, cortisol and thyroid hormone responses to chronic binge alcohol exposure throughout gestation: ovine model. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2608

Chicago Manual of Style (16th Edition):

Tress, Ursula. “Maternal adrenocorticotropin, cortisol and thyroid hormone responses to chronic binge alcohol exposure throughout gestation: ovine model.” 2009. Masters Thesis, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2608.

MLA Handbook (7th Edition):

Tress, Ursula. “Maternal adrenocorticotropin, cortisol and thyroid hormone responses to chronic binge alcohol exposure throughout gestation: ovine model.” 2009. Web. 24 Oct 2020.

Vancouver:

Tress U. Maternal adrenocorticotropin, cortisol and thyroid hormone responses to chronic binge alcohol exposure throughout gestation: ovine model. [Internet] [Masters thesis]. Texas A&M University; 2009. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2608.

Council of Science Editors:

Tress U. Maternal adrenocorticotropin, cortisol and thyroid hormone responses to chronic binge alcohol exposure throughout gestation: ovine model. [Masters Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2608


Texas A&M University

27. Gu, Xinsheng. Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics.

Degree: PhD, Toxicology, 2009, Texas A&M University

 Cytochrome P450 3A4 (CYP3A4) is a key enzyme responsible for the metabolism of drugs and endogenous compounds in human liver and intestine. CYP3A4 gene expression… (more)

Subjects/Keywords: cytochrome P450 3A4; Pregnane X Receptor

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APA (6th Edition):

Gu, X. (2009). Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1630

Chicago Manual of Style (16th Edition):

Gu, Xinsheng. “Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics.” 2009. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1630.

MLA Handbook (7th Edition):

Gu, Xinsheng. “Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics.” 2009. Web. 24 Oct 2020.

Vancouver:

Gu X. Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics. [Internet] [Doctoral dissertation]. Texas A&M University; 2009. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1630.

Council of Science Editors:

Gu X. Regulation of cytochrome P450 3A4 gene expression through modulating pregnane X receptor transcriptional activity by NF-ꢬ aryl hydrocarbon receptor and xenobiotics. [Doctoral Dissertation]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1630


Texas A&M University

28. Tan, Qiulin. Inhibition of cholesterol biosynthesis under hypoxia.

Degree: MS, Toxicology, 2006, Texas A&M University

 Oxygen balance is very important and tightly regulated in mammals. Under hypoxia, hypoxia inducible factor 1(HIF-1) dimerizes with hypoxia inducible factor 1± (HIF-) and activates… (more)

Subjects/Keywords: cholesterol; hypoxia

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APA (6th Edition):

Tan, Q. (2006). Inhibition of cholesterol biosynthesis under hypoxia. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/3101

Chicago Manual of Style (16th Edition):

Tan, Qiulin. “Inhibition of cholesterol biosynthesis under hypoxia.” 2006. Masters Thesis, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/3101.

MLA Handbook (7th Edition):

Tan, Qiulin. “Inhibition of cholesterol biosynthesis under hypoxia.” 2006. Web. 24 Oct 2020.

Vancouver:

Tan Q. Inhibition of cholesterol biosynthesis under hypoxia. [Internet] [Masters thesis]. Texas A&M University; 2006. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/3101.

Council of Science Editors:

Tan Q. Inhibition of cholesterol biosynthesis under hypoxia. [Masters Thesis]. Texas A&M University; 2006. Available from: http://hdl.handle.net/1969.1/3101


Texas A&M University

29. Suchodolski, Paulette F. Role of the Leucine Zipper of Marek's Disease Virus Oncoprotein Meq in Pathogenesis.

Degree: PhD, Veterinary Microbiology, 2010, Texas A&M University

 Marek's disease virus (MDV), the etiologic agent of Marek's disease, is a potent oncogenic herpesvirus. MDV is highly contagious and elicits a rapid onset of… (more)

Subjects/Keywords: Marek's; Herpesvirus; transformation; oncogene

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APA (6th Edition):

Suchodolski, P. F. (2010). Role of the Leucine Zipper of Marek's Disease Virus Oncoprotein Meq in Pathogenesis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-614

Chicago Manual of Style (16th Edition):

Suchodolski, Paulette F. “Role of the Leucine Zipper of Marek's Disease Virus Oncoprotein Meq in Pathogenesis.” 2010. Doctoral Dissertation, Texas A&M University. Accessed October 24, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-614.

MLA Handbook (7th Edition):

Suchodolski, Paulette F. “Role of the Leucine Zipper of Marek's Disease Virus Oncoprotein Meq in Pathogenesis.” 2010. Web. 24 Oct 2020.

Vancouver:

Suchodolski PF. Role of the Leucine Zipper of Marek's Disease Virus Oncoprotein Meq in Pathogenesis. [Internet] [Doctoral dissertation]. Texas A&M University; 2010. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-614.

Council of Science Editors:

Suchodolski PF. Role of the Leucine Zipper of Marek's Disease Virus Oncoprotein Meq in Pathogenesis. [Doctoral Dissertation]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-614

.