Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for +publisher:"Texas A&M University" +contributor:("Burghardt, Robert"). Showing records 1 – 30 of 98 total matches.

[1] [2] [3] [4]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

▼ Search Limiters


Texas A&M University

1. Castillo Bravo, Paula Andrea. Short Neuropeptide F Receptor in the Worker Brain of the Red Imported Fire Ant (Solenopsis invicta Buren) and Methodology for RNA Interference.

Degree: MS, Entomology, 2015, Texas A&M University

 The red imported fire ant (Solenopsis invicta Buren) is one of the worst invasive species in the United States. Investigating their physiology to understand its… (more)

Subjects/Keywords: Fire ants; short neuropeptide F; neuropeptides; RNAi; nutrient sensing; division of labor.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Castillo Bravo, P. A. (2015). Short Neuropeptide F Receptor in the Worker Brain of the Red Imported Fire Ant (Solenopsis invicta Buren) and Methodology for RNA Interference. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187456

Chicago Manual of Style (16th Edition):

Castillo Bravo, Paula Andrea. “Short Neuropeptide F Receptor in the Worker Brain of the Red Imported Fire Ant (Solenopsis invicta Buren) and Methodology for RNA Interference.” 2015. Masters Thesis, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/187456.

MLA Handbook (7th Edition):

Castillo Bravo, Paula Andrea. “Short Neuropeptide F Receptor in the Worker Brain of the Red Imported Fire Ant (Solenopsis invicta Buren) and Methodology for RNA Interference.” 2015. Web. 26 Oct 2020.

Vancouver:

Castillo Bravo PA. Short Neuropeptide F Receptor in the Worker Brain of the Red Imported Fire Ant (Solenopsis invicta Buren) and Methodology for RNA Interference. [Internet] [Masters thesis]. Texas A&M University; 2015. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/187456.

Council of Science Editors:

Castillo Bravo PA. Short Neuropeptide F Receptor in the Worker Brain of the Red Imported Fire Ant (Solenopsis invicta Buren) and Methodology for RNA Interference. [Masters Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/187456


Texas A&M University

2. Steinhauser, Chelsie Burroughs. Hexose Sugar Transport and Metabolism at the Porcine Uterine-Placental Interface.

Degree: PhD, Biomedical Sciences, 2015, Texas A&M University

 Commercial sows experience a high incidence of prenatal loss and substantial variation in birthweight among piglets in a litter. These outcomes negatively impact efficiency and… (more)

Subjects/Keywords: Pig; Pregnancy; Glucose; Fructose; Polyol Pathway; Endometrium; Placenta

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Steinhauser, C. B. (2015). Hexose Sugar Transport and Metabolism at the Porcine Uterine-Placental Interface. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156433

Chicago Manual of Style (16th Edition):

Steinhauser, Chelsie Burroughs. “Hexose Sugar Transport and Metabolism at the Porcine Uterine-Placental Interface.” 2015. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/156433.

MLA Handbook (7th Edition):

Steinhauser, Chelsie Burroughs. “Hexose Sugar Transport and Metabolism at the Porcine Uterine-Placental Interface.” 2015. Web. 26 Oct 2020.

Vancouver:

Steinhauser CB. Hexose Sugar Transport and Metabolism at the Porcine Uterine-Placental Interface. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/156433.

Council of Science Editors:

Steinhauser CB. Hexose Sugar Transport and Metabolism at the Porcine Uterine-Placental Interface. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156433


Texas A&M University

3. Williams, Diarra Kevin. In Vivo Models to Investigate Mechanisms of Rare Bone Pathologies and Therapeutic Treatment.

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

 Genetic disorders associated with skeletal disease are extremely complex and vary greatly in their clinical phenotypes. Thus, in vivo models that accurately recapitulate these rare… (more)

Subjects/Keywords: Hypophosphatasia; Down syndrome; sheep; CRISPR

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Williams, D. K. (2018). In Vivo Models to Investigate Mechanisms of Rare Bone Pathologies and Therapeutic Treatment. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174050

Chicago Manual of Style (16th Edition):

Williams, Diarra Kevin. “In Vivo Models to Investigate Mechanisms of Rare Bone Pathologies and Therapeutic Treatment.” 2018. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/174050.

MLA Handbook (7th Edition):

Williams, Diarra Kevin. “In Vivo Models to Investigate Mechanisms of Rare Bone Pathologies and Therapeutic Treatment.” 2018. Web. 26 Oct 2020.

Vancouver:

Williams DK. In Vivo Models to Investigate Mechanisms of Rare Bone Pathologies and Therapeutic Treatment. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/174050.

Council of Science Editors:

Williams DK. In Vivo Models to Investigate Mechanisms of Rare Bone Pathologies and Therapeutic Treatment. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/174050


Texas A&M University

4. Najjar, Kristina. Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach.

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

 For over 20 years, cell-penetrating peptides (CPPs) have been used as delivery vectors transporting macromolecules (cargos) into live cells for cell biology manipulations and therapeutic… (more)

Subjects/Keywords: Cell-penetrating peptides; Cell culture; Endocytic pathway

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Najjar, K. (2017). Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/165896

Chicago Manual of Style (16th Edition):

Najjar, Kristina. “Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach.” 2017. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/165896.

MLA Handbook (7th Edition):

Najjar, Kristina. “Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach.” 2017. Web. 26 Oct 2020.

Vancouver:

Najjar K. Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/165896.

Council of Science Editors:

Najjar K. Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/165896


Texas A&M University

5. Mukherjee, Atashi. Functionalized Zirconium Phosphate Nano Platelets - From Surface Design to Drug Delivery.

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

 The chemical characterization of nanomaterials in the realm of drug delivery and surface modification is on the current frontiers of analytical chemistry. A drug delivery… (more)

Subjects/Keywords: Inorganic layered nanomaterial; Drug Delivery; Secondary Ion Mass Spectrometry (SIMS); Zirconium Phosphate; Biocomposite nanomaterials; Surface Modification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mukherjee, A. (2014). Functionalized Zirconium Phosphate Nano Platelets - From Surface Design to Drug Delivery. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152537

Chicago Manual of Style (16th Edition):

Mukherjee, Atashi. “Functionalized Zirconium Phosphate Nano Platelets - From Surface Design to Drug Delivery.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/152537.

MLA Handbook (7th Edition):

Mukherjee, Atashi. “Functionalized Zirconium Phosphate Nano Platelets - From Surface Design to Drug Delivery.” 2014. Web. 26 Oct 2020.

Vancouver:

Mukherjee A. Functionalized Zirconium Phosphate Nano Platelets - From Surface Design to Drug Delivery. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/152537.

Council of Science Editors:

Mukherjee A. Functionalized Zirconium Phosphate Nano Platelets - From Surface Design to Drug Delivery. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152537


Texas A&M University

6. Sreenivasappa, Harini Bytaraya. Mechanical Signaling Induced Cellular Remodeling Studied By Integrated Optical And Atomic Force Microscopy.

Degree: PhD, Biomedical Engineering, 2014, Texas A&M University

 Vascular wall composition and mechanics are important for cardiovascular physiology and pathology. The reciprocal interaction between cells and their microenvironment influence cellular adaptation to external… (more)

Subjects/Keywords: Mechanotransduction; Adhesion force spectroscopy; cytoskeletal tension; RhoA pathway; RhoA - Src crosstalk; cell–matrix adhesions

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sreenivasappa, H. B. (2014). Mechanical Signaling Induced Cellular Remodeling Studied By Integrated Optical And Atomic Force Microscopy. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154022

Chicago Manual of Style (16th Edition):

Sreenivasappa, Harini Bytaraya. “Mechanical Signaling Induced Cellular Remodeling Studied By Integrated Optical And Atomic Force Microscopy.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/154022.

MLA Handbook (7th Edition):

Sreenivasappa, Harini Bytaraya. “Mechanical Signaling Induced Cellular Remodeling Studied By Integrated Optical And Atomic Force Microscopy.” 2014. Web. 26 Oct 2020.

Vancouver:

Sreenivasappa HB. Mechanical Signaling Induced Cellular Remodeling Studied By Integrated Optical And Atomic Force Microscopy. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/154022.

Council of Science Editors:

Sreenivasappa HB. Mechanical Signaling Induced Cellular Remodeling Studied By Integrated Optical And Atomic Force Microscopy. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154022


Texas A&M University

7. Turk, Harmony 1985-. The Role of Docosahexaenoic Acid in Regulation of Epidermal Growth Factor Receptor Activation and Function.

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

 The epidermal growth factor receptor (EGFR) is a transmembrane receptor tyrosine kinase integral in regulating cell growth, survival, and migration. EGFR signaling, which is dependent… (more)

Subjects/Keywords: signal transduction; Ras; colon cancer; n-3 polyunsaturated fatty acid; docosahexaenoic acid; lipid raft; epidermal growth factor receptor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Turk, H. 1. (2012). The Role of Docosahexaenoic Acid in Regulation of Epidermal Growth Factor Receptor Activation and Function. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148103

Chicago Manual of Style (16th Edition):

Turk, Harmony 1985-. “The Role of Docosahexaenoic Acid in Regulation of Epidermal Growth Factor Receptor Activation and Function.” 2012. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/148103.

MLA Handbook (7th Edition):

Turk, Harmony 1985-. “The Role of Docosahexaenoic Acid in Regulation of Epidermal Growth Factor Receptor Activation and Function.” 2012. Web. 26 Oct 2020.

Vancouver:

Turk H1. The Role of Docosahexaenoic Acid in Regulation of Epidermal Growth Factor Receptor Activation and Function. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/148103.

Council of Science Editors:

Turk H1. The Role of Docosahexaenoic Acid in Regulation of Epidermal Growth Factor Receptor Activation and Function. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148103


Texas A&M University

8. Gomez, Gabriel. Identification and Evaluation of Brucella Recombinant Outer Membrane Proteins as Subunit Vaccinogen Candidates in the Mouse Model of Brucellosis.

Degree: PhD, Veterinary Pathology, 2013, Texas A&M University

 Despite being amongst the most common zoonotic diseases in the world, brucellosis is a neglected disease for which an approved vaccine for human use does… (more)

Subjects/Keywords: Brucella; outer membrane proteins; vaccine; antigens; reverse vaccinology; mouse

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gomez, G. (2013). Identification and Evaluation of Brucella Recombinant Outer Membrane Proteins as Subunit Vaccinogen Candidates in the Mouse Model of Brucellosis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149282

Chicago Manual of Style (16th Edition):

Gomez, Gabriel. “Identification and Evaluation of Brucella Recombinant Outer Membrane Proteins as Subunit Vaccinogen Candidates in the Mouse Model of Brucellosis.” 2013. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/149282.

MLA Handbook (7th Edition):

Gomez, Gabriel. “Identification and Evaluation of Brucella Recombinant Outer Membrane Proteins as Subunit Vaccinogen Candidates in the Mouse Model of Brucellosis.” 2013. Web. 26 Oct 2020.

Vancouver:

Gomez G. Identification and Evaluation of Brucella Recombinant Outer Membrane Proteins as Subunit Vaccinogen Candidates in the Mouse Model of Brucellosis. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/149282.

Council of Science Editors:

Gomez G. Identification and Evaluation of Brucella Recombinant Outer Membrane Proteins as Subunit Vaccinogen Candidates in the Mouse Model of Brucellosis. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/149282


Texas A&M University

9. Nemec, Matthew James. Polyphenolics from Mango (Mangifera Indica L.) Suppress Breast Cancer Ductal Carcinoma In Situ Proliferation Both In Vitro And In Vivo: Potential Role of the IGFR-1-AKT-AMPK-mTOR-Signaling Axis.

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

 More than 25% of all newly diagnosed breast cancer cases are ductal carcinoma in situ (DCIS), the most commonly diagnosed form of non-invasive breast cancer.… (more)

Subjects/Keywords: AMPK; mTOR; polyphenols; DCIS; breast cancer; mangos; pyrogallol

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nemec, M. J. (2016). Polyphenolics from Mango (Mangifera Indica L.) Suppress Breast Cancer Ductal Carcinoma In Situ Proliferation Both In Vitro And In Vivo: Potential Role of the IGFR-1-AKT-AMPK-mTOR-Signaling Axis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158043

Chicago Manual of Style (16th Edition):

Nemec, Matthew James. “Polyphenolics from Mango (Mangifera Indica L.) Suppress Breast Cancer Ductal Carcinoma In Situ Proliferation Both In Vitro And In Vivo: Potential Role of the IGFR-1-AKT-AMPK-mTOR-Signaling Axis.” 2016. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/158043.

MLA Handbook (7th Edition):

Nemec, Matthew James. “Polyphenolics from Mango (Mangifera Indica L.) Suppress Breast Cancer Ductal Carcinoma In Situ Proliferation Both In Vitro And In Vivo: Potential Role of the IGFR-1-AKT-AMPK-mTOR-Signaling Axis.” 2016. Web. 26 Oct 2020.

Vancouver:

Nemec MJ. Polyphenolics from Mango (Mangifera Indica L.) Suppress Breast Cancer Ductal Carcinoma In Situ Proliferation Both In Vitro And In Vivo: Potential Role of the IGFR-1-AKT-AMPK-mTOR-Signaling Axis. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/158043.

Council of Science Editors:

Nemec MJ. Polyphenolics from Mango (Mangifera Indica L.) Suppress Breast Cancer Ductal Carcinoma In Situ Proliferation Both In Vitro And In Vivo: Potential Role of the IGFR-1-AKT-AMPK-mTOR-Signaling Axis. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158043


Texas A&M University

10. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 26, 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. 26 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 26]. 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

11. Allen, Carolyn C. Influence of Nutrition during the Juvenile Period on Gene Expression Within the Hypothalamic Arcuate Nucleus and on Age at Puberty in Heifers.

Degree: MS, Physiology of Reproduction, 2011, Texas A&M University

 Developmental changes within the hypothalamus are necessary for maturation of the reproductive neuroendocrine axis. Recent reports have implicated several neuronal networks in this process, but… (more)

Subjects/Keywords: Puberty; Arcuate Nucleus; Heifers; Neuropeptide Y; Leptin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Allen, C. C. (2011). Influence of Nutrition during the Juvenile Period on Gene Expression Within the Hypothalamic Arcuate Nucleus and on Age at Puberty in Heifers. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8522

Chicago Manual of Style (16th Edition):

Allen, Carolyn C. “Influence of Nutrition during the Juvenile Period on Gene Expression Within the Hypothalamic Arcuate Nucleus and on Age at Puberty in Heifers.” 2011. Masters Thesis, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8522.

MLA Handbook (7th Edition):

Allen, Carolyn C. “Influence of Nutrition during the Juvenile Period on Gene Expression Within the Hypothalamic Arcuate Nucleus and on Age at Puberty in Heifers.” 2011. Web. 26 Oct 2020.

Vancouver:

Allen CC. Influence of Nutrition during the Juvenile Period on Gene Expression Within the Hypothalamic Arcuate Nucleus and on Age at Puberty in Heifers. [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8522.

Council of Science Editors:

Allen CC. Influence of Nutrition during the Juvenile Period on Gene Expression Within the Hypothalamic Arcuate Nucleus and on Age at Puberty in Heifers. [Masters Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8522


Texas A&M University

12. Krishnaveni Sivakumar, Kirthiram. Molecular Mechanisms of Hexavalent Chromium-Induced Premature Ovarian Failure.

Degree: PhD, Toxicology, 2018, Texas A&M University

 Environmental exposure to endocrine-disrupting chemicals (EDCs) is one of the causes of premature ovarian failure (POF). Hexavalent chromium (CrVI) is a heavy metal EDC widely… (more)

Subjects/Keywords: ovary; chromium; premature ovarian failure; primordial follicle; germ cell nest breakdown

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Krishnaveni Sivakumar, K. (2018). Molecular Mechanisms of Hexavalent Chromium-Induced Premature Ovarian Failure. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174136

Chicago Manual of Style (16th Edition):

Krishnaveni Sivakumar, Kirthiram. “Molecular Mechanisms of Hexavalent Chromium-Induced Premature Ovarian Failure.” 2018. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/174136.

MLA Handbook (7th Edition):

Krishnaveni Sivakumar, Kirthiram. “Molecular Mechanisms of Hexavalent Chromium-Induced Premature Ovarian Failure.” 2018. Web. 26 Oct 2020.

Vancouver:

Krishnaveni Sivakumar K. Molecular Mechanisms of Hexavalent Chromium-Induced Premature Ovarian Failure. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/174136.

Council of Science Editors:

Krishnaveni Sivakumar K. Molecular Mechanisms of Hexavalent Chromium-Induced Premature Ovarian Failure. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/174136


Texas A&M University

13. Li, Xilong. Regulation of Porcine Conceptus Survival and Growth by L-arginine.

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

 This study was conducted to test the hypothesis that dietary supplementation with L-arginine during early pregnancy will ameliorate embryonic loss in pigs. Gilts were bred… (more)

Subjects/Keywords: Arginine; early pregnancy; embryonic survival; mechanism

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, X. (2012). Regulation of Porcine Conceptus Survival and Growth by L-arginine. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10541

Chicago Manual of Style (16th Edition):

Li, Xilong. “Regulation of Porcine Conceptus Survival and Growth by L-arginine.” 2012. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10541.

MLA Handbook (7th Edition):

Li, Xilong. “Regulation of Porcine Conceptus Survival and Growth by L-arginine.” 2012. Web. 26 Oct 2020.

Vancouver:

Li X. Regulation of Porcine Conceptus Survival and Growth by L-arginine. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10541.

Council of Science Editors:

Li X. Regulation of Porcine Conceptus Survival and Growth by L-arginine. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10541


Texas A&M University

14. Li, Xi. Mechanism of Action of Sulindac and Diindolylmethane Analogs as Anticancer Agents.

Degree: PhD, Medical Sciences, 2014, Texas A&M University

 Cancer accounts for one in eight deaths worldwide and one in four deaths in the United States. Chemotherapy is the most common treatment option for… (more)

Subjects/Keywords: Cancer; Colon Cancer; Pancreatic Cancer; Sulindac; NSAID; Di-indolylmethane; C-DIM; Sp; Specificity Protein; Nuclear Receptor; NR4A; NR4A1; NR4A2; Nurr1; TR3; Nur77; Transactivation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, X. (2014). Mechanism of Action of Sulindac and Diindolylmethane Analogs as Anticancer Agents. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158901

Chicago Manual of Style (16th Edition):

Li, Xi. “Mechanism of Action of Sulindac and Diindolylmethane Analogs as Anticancer Agents.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/158901.

MLA Handbook (7th Edition):

Li, Xi. “Mechanism of Action of Sulindac and Diindolylmethane Analogs as Anticancer Agents.” 2014. Web. 26 Oct 2020.

Vancouver:

Li X. Mechanism of Action of Sulindac and Diindolylmethane Analogs as Anticancer Agents. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/158901.

Council of Science Editors:

Li X. Mechanism of Action of Sulindac and Diindolylmethane Analogs as Anticancer Agents. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/158901


Texas A&M University

15. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 26, 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. 26 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 26]. 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


Texas A&M University

16. Pena Maceda, Bruno. New Directions for Cancer Drug Research of Ruthenium and Rhodium Compounds: Investigation of Cytotoxicities, Mechanisms of Cancer Cell Death, and Cellular Targets.

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

 The discovery of the antitumor properties of cisplatin revolutionized the field of medicinal inorganic chemistry and fostered the development of metal-based anticancer drugs, a topic… (more)

Subjects/Keywords: ruthenium; rhodium; anticancer drugs; cancer; chemotherapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pena Maceda, B. (2014). New Directions for Cancer Drug Research of Ruthenium and Rhodium Compounds: Investigation of Cytotoxicities, Mechanisms of Cancer Cell Death, and Cellular Targets. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153355

Chicago Manual of Style (16th Edition):

Pena Maceda, Bruno. “New Directions for Cancer Drug Research of Ruthenium and Rhodium Compounds: Investigation of Cytotoxicities, Mechanisms of Cancer Cell Death, and Cellular Targets.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/153355.

MLA Handbook (7th Edition):

Pena Maceda, Bruno. “New Directions for Cancer Drug Research of Ruthenium and Rhodium Compounds: Investigation of Cytotoxicities, Mechanisms of Cancer Cell Death, and Cellular Targets.” 2014. Web. 26 Oct 2020.

Vancouver:

Pena Maceda B. New Directions for Cancer Drug Research of Ruthenium and Rhodium Compounds: Investigation of Cytotoxicities, Mechanisms of Cancer Cell Death, and Cellular Targets. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/153355.

Council of Science Editors:

Pena Maceda B. New Directions for Cancer Drug Research of Ruthenium and Rhodium Compounds: Investigation of Cytotoxicities, Mechanisms of Cancer Cell Death, and Cellular Targets. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153355


Texas A&M University

17. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 26, 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. 26 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 26]. 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

18. Frank, James William. Characterization of Integrins and Osteopontin at the Uterine-Placental Interface During Pregnancy in Pigs and Sheep.

Degree: PhD, Biomedical Sciences, 2015, Texas A&M University

 Establishment of a successful pregnancy is dependent upon proper communication between the conceptus and uterus and provides the critical physiological and anatomical groundwork required to… (more)

Subjects/Keywords: Osteopontin; Integrin; Focal Adhesion; Implantation; Pregnancy; Pig; Sheep

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Frank, J. W. (2015). Characterization of Integrins and Osteopontin at the Uterine-Placental Interface During Pregnancy in Pigs and Sheep. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155153

Chicago Manual of Style (16th Edition):

Frank, James William. “Characterization of Integrins and Osteopontin at the Uterine-Placental Interface During Pregnancy in Pigs and Sheep.” 2015. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/155153.

MLA Handbook (7th Edition):

Frank, James William. “Characterization of Integrins and Osteopontin at the Uterine-Placental Interface During Pregnancy in Pigs and Sheep.” 2015. Web. 26 Oct 2020.

Vancouver:

Frank JW. Characterization of Integrins and Osteopontin at the Uterine-Placental Interface During Pregnancy in Pigs and Sheep. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/155153.

Council of Science Editors:

Frank JW. Characterization of Integrins and Osteopontin at the Uterine-Placental Interface During Pregnancy in Pigs and Sheep. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155153


Texas A&M University

19. Lee, Je Hoon. Cellular Transport of Prostaglandins in the Ovine Uterus.

Degree: PhD, Biomedical Sciences, 2013, Texas A&M University

 In ruminants, prostaglandin F2 alpha (PGF2α) is released from the endometrium in a pulsatile pattern at the time of luteolysis. The luteolytic PGF2α pulses are… (more)

Subjects/Keywords: prostaglandin F2 alpha (PGF2α); prostaglandin transporter (PGT); utero-ovarian plexus (UOP); corpus luteum (CL); luteolysis; interferon tau (IFNT); PGT-mediated mechanism; endometrium; ruminants

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lee, J. H. (2013). Cellular Transport of Prostaglandins in the Ovine Uterus. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149417

Chicago Manual of Style (16th Edition):

Lee, Je Hoon. “Cellular Transport of Prostaglandins in the Ovine Uterus.” 2013. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/149417.

MLA Handbook (7th Edition):

Lee, Je Hoon. “Cellular Transport of Prostaglandins in the Ovine Uterus.” 2013. Web. 26 Oct 2020.

Vancouver:

Lee JH. Cellular Transport of Prostaglandins in the Ovine Uterus. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/149417.

Council of Science Editors:

Lee JH. Cellular Transport of Prostaglandins in the Ovine Uterus. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/149417


Texas A&M University

20. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 26, 2020. http://hdl.handle.net/1969.1/151011.

MLA Handbook (7th Edition):

Sreevalsan, Sandeep. “Molecular Mechanisms of Cannabinoids as Anti-cancer Agents.” 2013. Web. 26 Oct 2020.

Vancouver:

Sreevalsan S. Molecular Mechanisms of Cannabinoids as Anti-cancer Agents. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Oct 26]. 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


Texas A&M University

21. Jose, Jiney. Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles.

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

 Water-soluble fluorescent probes with emission in the 600-800 nm region have significant potential in biological applications such as cell imaging. Most fluorescent probes however suffer… (more)

Subjects/Keywords: Fluorescent dyes; nanoparticles

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jose, J. (2011). Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334

Chicago Manual of Style (16th Edition):

Jose, Jiney. “Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles.” 2011. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334.

MLA Handbook (7th Edition):

Jose, Jiney. “Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles.” 2011. Web. 26 Oct 2020.

Vancouver:

Jose J. Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334.

Council of Science Editors:

Jose J. Synthesis of Through-bond Energy Transfer Cassettes and Their Encapsulation in Silica and Calcium Phosphate Nanoparticles. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7334


Texas A&M University

22. Tang, Leung Kau. Modulation of Endothelial Cytoskeletal Dynamics and YAP Localization by Angiogenic Factors.

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

 Angiogenesis, the formation of new blood vessels from pre-existing ones, plays a crucial role in physiological processes and various pathological conditions including cancer. Angiogenic factor… (more)

Subjects/Keywords: Gab1; Nck; YAP; Actin remodeling; VE-cadherin cell-cell adhesion; Endothelial cells; Angiogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tang, L. K. (2017). Modulation of Endothelial Cytoskeletal Dynamics and YAP Localization by Angiogenic Factors. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174764

Chicago Manual of Style (16th Edition):

Tang, Leung Kau. “Modulation of Endothelial Cytoskeletal Dynamics and YAP Localization by Angiogenic Factors.” 2017. Masters Thesis, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/174764.

MLA Handbook (7th Edition):

Tang, Leung Kau. “Modulation of Endothelial Cytoskeletal Dynamics and YAP Localization by Angiogenic Factors.” 2017. Web. 26 Oct 2020.

Vancouver:

Tang LK. Modulation of Endothelial Cytoskeletal Dynamics and YAP Localization by Angiogenic Factors. [Internet] [Masters thesis]. Texas A&M University; 2017. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/174764.

Council of Science Editors:

Tang LK. Modulation of Endothelial Cytoskeletal Dynamics and YAP Localization by Angiogenic Factors. [Masters Thesis]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/174764


Texas A&M University

23. Chang, Cheng-An Richard. The Epigenetic Effects of Preconception Paternal Alcohol Exposure on Adult Health and Disease.

Degree: PhD, Biomedical Sciences, 2019, Texas A&M University

 Alcohol is a notorious teratogen and a major driver of both mental and physical defects. Recently, alcohol has been discovered to exert intergenerational effects on… (more)

Subjects/Keywords: Epigenetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chang, C. R. (2019). The Epigenetic Effects of Preconception Paternal Alcohol Exposure on Adult Health and Disease. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/188715

Chicago Manual of Style (16th Edition):

Chang, Cheng-An Richard. “The Epigenetic Effects of Preconception Paternal Alcohol Exposure on Adult Health and Disease.” 2019. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/188715.

MLA Handbook (7th Edition):

Chang, Cheng-An Richard. “The Epigenetic Effects of Preconception Paternal Alcohol Exposure on Adult Health and Disease.” 2019. Web. 26 Oct 2020.

Vancouver:

Chang CR. The Epigenetic Effects of Preconception Paternal Alcohol Exposure on Adult Health and Disease. [Internet] [Doctoral dissertation]. Texas A&M University; 2019. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/188715.

Council of Science Editors:

Chang CR. The Epigenetic Effects of Preconception Paternal Alcohol Exposure on Adult Health and Disease. [Doctoral Dissertation]. Texas A&M University; 2019. Available from: http://hdl.handle.net/1969.1/188715

24. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 26, 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. 26 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 26]. 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

25. Johnson, Gregory Andrew. Targeted Killing of Bacteria by Conjugation of a Soluble Photosensitizer to an Antimicrobial Peptide: Priniciples and Mechanisms.

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

 Antimicrobial peptides (AMPs) and photosensitizers (PS) have gained attention as potential alternatives to traditional antibiotics for the treatment of microbial infection due to the decreased… (more)

Subjects/Keywords: antimicrobial pepitde; AMP; photosensitizer; photodynamic inactivation; antimicrobial photodynamic therapy; aPDT

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Johnson, G. A. (2013). Targeted Killing of Bacteria by Conjugation of a Soluble Photosensitizer to an Antimicrobial Peptide: Priniciples and Mechanisms. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151183

Chicago Manual of Style (16th Edition):

Johnson, Gregory Andrew. “Targeted Killing of Bacteria by Conjugation of a Soluble Photosensitizer to an Antimicrobial Peptide: Priniciples and Mechanisms.” 2013. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/151183.

MLA Handbook (7th Edition):

Johnson, Gregory Andrew. “Targeted Killing of Bacteria by Conjugation of a Soluble Photosensitizer to an Antimicrobial Peptide: Priniciples and Mechanisms.” 2013. Web. 26 Oct 2020.

Vancouver:

Johnson GA. Targeted Killing of Bacteria by Conjugation of a Soluble Photosensitizer to an Antimicrobial Peptide: Priniciples and Mechanisms. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/151183.

Council of Science Editors:

Johnson GA. Targeted Killing of Bacteria by Conjugation of a Soluble Photosensitizer to an Antimicrobial Peptide: Priniciples and Mechanisms. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151183

26. Guthrie, Aaron S 1987-. Phenethyl Isothiocyanate (PEITC) Decreases Specficity Protein (SP) Tanscription Factors through an ROS-dependent Mechanism.

Degree: MS, Biochemistry, 2012, Texas A&M University

 Isothiocyanates (ITCs) are phytochemicals highly expressed in cruciferous vegetables and these compounds are associated with the decreased incidence of cancers in populations consuming high levels… (more)

Subjects/Keywords: Sp transcription factors; Sp dependent genes; ROS; PEITC

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Guthrie, A. S. 1. (2012). Phenethyl Isothiocyanate (PEITC) Decreases Specficity Protein (SP) Tanscription Factors through an ROS-dependent Mechanism. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148086

Chicago Manual of Style (16th Edition):

Guthrie, Aaron S 1987-. “Phenethyl Isothiocyanate (PEITC) Decreases Specficity Protein (SP) Tanscription Factors through an ROS-dependent Mechanism.” 2012. Masters Thesis, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/148086.

MLA Handbook (7th Edition):

Guthrie, Aaron S 1987-. “Phenethyl Isothiocyanate (PEITC) Decreases Specficity Protein (SP) Tanscription Factors through an ROS-dependent Mechanism.” 2012. Web. 26 Oct 2020.

Vancouver:

Guthrie AS1. Phenethyl Isothiocyanate (PEITC) Decreases Specficity Protein (SP) Tanscription Factors through an ROS-dependent Mechanism. [Internet] [Masters thesis]. Texas A&M University; 2012. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/148086.

Council of Science Editors:

Guthrie AS1. Phenethyl Isothiocyanate (PEITC) Decreases Specficity Protein (SP) Tanscription Factors through an ROS-dependent Mechanism. [Masters Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148086

27. Lacey, Alexandra Dianne. NR4A1 Antagonists Target the Oncogenic PAX3-FOXO1A Gene and Induce Interleukin -24 in Rhabdomyosarcoma (RMS).

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

 Rhabdomyosarcoma (RMS) is a pediatric cancer for which common therapeutics include cytotoxic chemotherapeutics that result in adverse health outcomes later in adulthood. Previous studies have… (more)

Subjects/Keywords: Rhabdomyosarcoma; Pediatric cancer; orphan nuclear receptor; NR4A1; PAX3-FOXO1A; Interleukin-24

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lacey, A. D. (2017). NR4A1 Antagonists Target the Oncogenic PAX3-FOXO1A Gene and Induce Interleukin -24 in Rhabdomyosarcoma (RMS). (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/166039

Chicago Manual of Style (16th Edition):

Lacey, Alexandra Dianne. “NR4A1 Antagonists Target the Oncogenic PAX3-FOXO1A Gene and Induce Interleukin -24 in Rhabdomyosarcoma (RMS).” 2017. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/166039.

MLA Handbook (7th Edition):

Lacey, Alexandra Dianne. “NR4A1 Antagonists Target the Oncogenic PAX3-FOXO1A Gene and Induce Interleukin -24 in Rhabdomyosarcoma (RMS).” 2017. Web. 26 Oct 2020.

Vancouver:

Lacey AD. NR4A1 Antagonists Target the Oncogenic PAX3-FOXO1A Gene and Induce Interleukin -24 in Rhabdomyosarcoma (RMS). [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/166039.

Council of Science Editors:

Lacey AD. NR4A1 Antagonists Target the Oncogenic PAX3-FOXO1A Gene and Induce Interleukin -24 in Rhabdomyosarcoma (RMS). [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/166039

28. Clubb, Aaron Bryant. Characterization of Nano-Environments by Hypervelocity Projectile Secondary Ion Mass Spectrometry.

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

 The purpose of this study was to explore the performance of a secondary ion mass spectrometry (SIMS) technique for probing nanovolumes. The variant of SIMS… (more)

Subjects/Keywords: Secondary Ion Mass Spectrometry; SIMS; surface; clusters; nanoparticles; graphene

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Clubb, A. B. (2017). Characterization of Nano-Environments by Hypervelocity Projectile Secondary Ion Mass Spectrometry. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161352

Chicago Manual of Style (16th Edition):

Clubb, Aaron Bryant. “Characterization of Nano-Environments by Hypervelocity Projectile Secondary Ion Mass Spectrometry.” 2017. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/161352.

MLA Handbook (7th Edition):

Clubb, Aaron Bryant. “Characterization of Nano-Environments by Hypervelocity Projectile Secondary Ion Mass Spectrometry.” 2017. Web. 26 Oct 2020.

Vancouver:

Clubb AB. Characterization of Nano-Environments by Hypervelocity Projectile Secondary Ion Mass Spectrometry. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/161352.

Council of Science Editors:

Clubb AB. Characterization of Nano-Environments by Hypervelocity Projectile Secondary Ion Mass Spectrometry. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/161352

29. Morris, David Christopher. The Role of Nck in Breast Carcinoma Cell Invasion and Metastasis.

Degree: PhD, Veterinary Microbiology, 2015, Texas A&M University

 The high incidence of invasive breast carcinomas, which accounts for about 90% of all breast cancer-related deaths, underscores the need for new and more effective… (more)

Subjects/Keywords: Nck; breast cancer; metastasis; invadopodia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Morris, D. C. (2015). The Role of Nck in Breast Carcinoma Cell Invasion and Metastasis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155550

Chicago Manual of Style (16th Edition):

Morris, David Christopher. “The Role of Nck in Breast Carcinoma Cell Invasion and Metastasis.” 2015. Doctoral Dissertation, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/155550.

MLA Handbook (7th Edition):

Morris, David Christopher. “The Role of Nck in Breast Carcinoma Cell Invasion and Metastasis.” 2015. Web. 26 Oct 2020.

Vancouver:

Morris DC. The Role of Nck in Breast Carcinoma Cell Invasion and Metastasis. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/155550.

Council of Science Editors:

Morris DC. The Role of Nck in Breast Carcinoma Cell Invasion and Metastasis. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155550

30. Wing, Theodore. Two Novel Mechanistic Paradigms in Pig Pregnancy: I. Osteopontin Binds to the ITGAV (the αv Integrin Subunit) to Promote Porcine Endothelial Progenitor Cell Incorporation into Developing Vasculature. II. Expression and Regulation of Genes for Glucose and Arginine Transporters in Pig Uteri, Conceptuses and Placentae Increases during Pregnancy.

Degree: MS, Biomedical Sciences, 2013, Texas A&M University

 During pregnancy, uterine and placental blood vessels develop to facilitate maximal transfer of nutrients to the fetus. These studies focus on the incorporation of endothelial… (more)

Subjects/Keywords: Endothelial progenitor cell

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wing, T. (2013). Two Novel Mechanistic Paradigms in Pig Pregnancy: I. Osteopontin Binds to the ITGAV (the αv Integrin Subunit) to Promote Porcine Endothelial Progenitor Cell Incorporation into Developing Vasculature. II. Expression and Regulation of Genes for Glucose and Arginine Transporters in Pig Uteri, Conceptuses and Placentae Increases during Pregnancy. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151826

Chicago Manual of Style (16th Edition):

Wing, Theodore. “Two Novel Mechanistic Paradigms in Pig Pregnancy: I. Osteopontin Binds to the ITGAV (the αv Integrin Subunit) to Promote Porcine Endothelial Progenitor Cell Incorporation into Developing Vasculature. II. Expression and Regulation of Genes for Glucose and Arginine Transporters in Pig Uteri, Conceptuses and Placentae Increases during Pregnancy.” 2013. Masters Thesis, Texas A&M University. Accessed October 26, 2020. http://hdl.handle.net/1969.1/151826.

MLA Handbook (7th Edition):

Wing, Theodore. “Two Novel Mechanistic Paradigms in Pig Pregnancy: I. Osteopontin Binds to the ITGAV (the αv Integrin Subunit) to Promote Porcine Endothelial Progenitor Cell Incorporation into Developing Vasculature. II. Expression and Regulation of Genes for Glucose and Arginine Transporters in Pig Uteri, Conceptuses and Placentae Increases during Pregnancy.” 2013. Web. 26 Oct 2020.

Vancouver:

Wing T. Two Novel Mechanistic Paradigms in Pig Pregnancy: I. Osteopontin Binds to the ITGAV (the αv Integrin Subunit) to Promote Porcine Endothelial Progenitor Cell Incorporation into Developing Vasculature. II. Expression and Regulation of Genes for Glucose and Arginine Transporters in Pig Uteri, Conceptuses and Placentae Increases during Pregnancy. [Internet] [Masters thesis]. Texas A&M University; 2013. [cited 2020 Oct 26]. Available from: http://hdl.handle.net/1969.1/151826.

Council of Science Editors:

Wing T. Two Novel Mechanistic Paradigms in Pig Pregnancy: I. Osteopontin Binds to the ITGAV (the αv Integrin Subunit) to Promote Porcine Endothelial Progenitor Cell Incorporation into Developing Vasculature. II. Expression and Regulation of Genes for Glucose and Arginine Transporters in Pig Uteri, Conceptuses and Placentae Increases during Pregnancy. [Masters Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151826

[1] [2] [3] [4]

.