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Dept: Biochemistry  University: Virginia Commonwealth University

You searched for subject:( 1 5 ). Showing records 1 – 13 of 13 total matches.

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Virginia Commonwealth University

1. Sukholutsky, Marianna. ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES.

Degree: MS, Biochemistry, 2010, Virginia Commonwealth University

 Our recent studies have shown a link between Adenovirus-5 (Ad-5) and elevated lipids, which prompted the hypothesis that Ad-5 infection might augment hepatic and/or adipose… (more)

Subjects/Keywords: lipid metabolism; Ad-5; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Sukholutsky, M. (2010). ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2297

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

Chicago Manual of Style (16th Edition):

Sukholutsky, Marianna. “ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES.” 2010. Thesis, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/2297.

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

MLA Handbook (7th Edition):

Sukholutsky, Marianna. “ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES.” 2010. Web. 21 Nov 2019.

Vancouver:

Sukholutsky M. ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES. [Internet] [Thesis]. Virginia Commonwealth University; 2010. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/2297.

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

Council of Science Editors:

Sukholutsky M. ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES. [Thesis]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/2297

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


Virginia Commonwealth University

2. Hobbs, Daniel. PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY.

Degree: MS, Biochemistry, 2010, Virginia Commonwealth University

 Phosphodiesterase Type 5 (PDE5) inhibitors are cardioprotective against ischemia/reperfusion (I/R) injury. However, it remains uncertain if I/R affects PDE5. We hypothesized that generation of reactive… (more)

Subjects/Keywords: Phosphodiesterase 5; Ischemia/Reperfusion Injury; Reactive Oxygen Species; Pharmacological Preconditioning; cGMP-Dependent Protein Kinase; Myocardial Infarction; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Hobbs, D. (2010). PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/106

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

Chicago Manual of Style (16th Edition):

Hobbs, Daniel. “PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY.” 2010. Thesis, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/106.

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

MLA Handbook (7th Edition):

Hobbs, Daniel. “PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY.” 2010. Web. 21 Nov 2019.

Vancouver:

Hobbs D. PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY. [Internet] [Thesis]. Virginia Commonwealth University; 2010. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/106.

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

Council of Science Editors:

Hobbs D. PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY. [Thesis]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/106

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


Virginia Commonwealth University

3. Anand, Monika. FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME.

Degree: PhD, Biochemistry, 2010, Virginia Commonwealth University

 Glioblastoma Multiforme (GBM) is an aggressive and fatal cancer of the brain. It is characterized with augmented morbidity and elusion to therapies due in part… (more)

Subjects/Keywords: GBM; MMP-1; Invasion; EGFR; MAPK; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Anand, M. (2010). FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2214

Chicago Manual of Style (16th Edition):

Anand, Monika. “FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME.” 2010. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/2214.

MLA Handbook (7th Edition):

Anand, Monika. “FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME.” 2010. Web. 21 Nov 2019.

Vancouver:

Anand M. FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2010. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/2214.

Council of Science Editors:

Anand M. FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME. [Doctoral Dissertation]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/2214


Virginia Commonwealth University

4. Gomez-Arroyo, Jose. Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension.

Degree: PhD, Biochemistry, 2013, Virginia Commonwealth University

 Right ventricular dysfunction is the most frequent cause of death in patients with pulmonary arterial hypertension. Although abnormal energy substrate use has been implicated in… (more)

Subjects/Keywords: PGC-1; mitochondria; right ventricle; right ventricular failure; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Gomez-Arroyo, J. (2013). Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3257

Chicago Manual of Style (16th Edition):

Gomez-Arroyo, Jose. “Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension.” 2013. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/3257.

MLA Handbook (7th Edition):

Gomez-Arroyo, Jose. “Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension.” 2013. Web. 21 Nov 2019.

Vancouver:

Gomez-Arroyo J. Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2013. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/3257.

Council of Science Editors:

Gomez-Arroyo J. Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension. [Doctoral Dissertation]. Virginia Commonwealth University; 2013. Available from: https://scholarscompass.vcu.edu/etd/3257


Virginia Commonwealth University

5. Price, Megan. Sphingosine-1-phosphate in mast cell-mediated allergic responses.

Degree: PhD, Biochemistry, 2011, Virginia Commonwealth University

 Mast cells play a critical role in both acute and chronic inflammation and mature in peripheral tissues from bone marrow-derived progenitors that circulate in the… (more)

Subjects/Keywords: sphingosine-1-phosphate; sphingosine kinase; mast cells; chymase; NF-kB; airway hyperresponsiveness; asthma; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Price, M. (2011). Sphingosine-1-phosphate in mast cell-mediated allergic responses. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/254

Chicago Manual of Style (16th Edition):

Price, Megan. “Sphingosine-1-phosphate in mast cell-mediated allergic responses.” 2011. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/254.

MLA Handbook (7th Edition):

Price, Megan. “Sphingosine-1-phosphate in mast cell-mediated allergic responses.” 2011. Web. 21 Nov 2019.

Vancouver:

Price M. Sphingosine-1-phosphate in mast cell-mediated allergic responses. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2011. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/254.

Council of Science Editors:

Price M. Sphingosine-1-phosphate in mast cell-mediated allergic responses. [Doctoral Dissertation]. Virginia Commonwealth University; 2011. Available from: https://scholarscompass.vcu.edu/etd/254


Virginia Commonwealth University

6. Bryan, Lauren. Novel Mechanisms Regulating Cytokine-induced Gene Expression in Astrocytes and Glioblastoma Cells.

Degree: PhD, Biochemistry, 2009, Virginia Commonwealth University

 Chronic inflammation in the brain results in the development of several CNS diseases, including Alzheimer’s and Parkinson’s diseases, multiple sclerosis, and tumors. IL-1, a pro-inflammatory… (more)

Subjects/Keywords: astrocytes; glioblastoma; interleukin-1; sphingosine-1-phosphate; plasminogen activator system; chemokines; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Bryan, L. (2009). Novel Mechanisms Regulating Cytokine-induced Gene Expression in Astrocytes and Glioblastoma Cells. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1687

Chicago Manual of Style (16th Edition):

Bryan, Lauren. “Novel Mechanisms Regulating Cytokine-induced Gene Expression in Astrocytes and Glioblastoma Cells.” 2009. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/1687.

MLA Handbook (7th Edition):

Bryan, Lauren. “Novel Mechanisms Regulating Cytokine-induced Gene Expression in Astrocytes and Glioblastoma Cells.” 2009. Web. 21 Nov 2019.

Vancouver:

Bryan L. Novel Mechanisms Regulating Cytokine-induced Gene Expression in Astrocytes and Glioblastoma Cells. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2009. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/1687.

Council of Science Editors:

Bryan L. Novel Mechanisms Regulating Cytokine-induced Gene Expression in Astrocytes and Glioblastoma Cells. [Doctoral Dissertation]. Virginia Commonwealth University; 2009. Available from: https://scholarscompass.vcu.edu/etd/1687


Virginia Commonwealth University

7. Wilczynska, Katarzyna Marta. Inflammation-associated gene regulation in primary astrocytes, glial tumors and cellular differentiation.

Degree: PhD, Biochemistry, 2008, Virginia Commonwealth University

 This dissertation elucidates several independent molecular mechanisms that function in astrocytes and glial tumor cells, and suggest that developmental and inflammatory signals may contribute to… (more)

Subjects/Keywords: astrocytes; inflammation; brain tumors; TIMP-1; STAT3; NFI; IL-1; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Wilczynska, K. M. (2008). Inflammation-associated gene regulation in primary astrocytes, glial tumors and cellular differentiation. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1113

Chicago Manual of Style (16th Edition):

Wilczynska, Katarzyna Marta. “Inflammation-associated gene regulation in primary astrocytes, glial tumors and cellular differentiation.” 2008. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/1113.

MLA Handbook (7th Edition):

Wilczynska, Katarzyna Marta. “Inflammation-associated gene regulation in primary astrocytes, glial tumors and cellular differentiation.” 2008. Web. 21 Nov 2019.

Vancouver:

Wilczynska KM. Inflammation-associated gene regulation in primary astrocytes, glial tumors and cellular differentiation. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2008. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/1113.

Council of Science Editors:

Wilczynska KM. Inflammation-associated gene regulation in primary astrocytes, glial tumors and cellular differentiation. [Doctoral Dissertation]. Virginia Commonwealth University; 2008. Available from: https://scholarscompass.vcu.edu/etd/1113


Virginia Commonwealth University

8. Youssefian, Leena. THE SMALL MOLECULE BCL-2 INHIBITOR HA14-1 POTENTIATES THE LETHALITY OF A REGIMEN COMBINING MEK1/2 AND CHK1 INHIBITORS IN MULTIPLE MYELOMA CELLS.

Degree: MS, Biochemistry, 2009, Virginia Commonwealth University

 Previously, we have found that the co-administration of MEK1/2 inhibitors and Chk1 inhibitors synergistically induce multiple myeloma cell apoptosis through upregulation of the BH3-only pro-apoptotic… (more)

Subjects/Keywords: Multiple myeloma; HA14-1; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Youssefian, L. (2009). THE SMALL MOLECULE BCL-2 INHIBITOR HA14-1 POTENTIATES THE LETHALITY OF A REGIMEN COMBINING MEK1/2 AND CHK1 INHIBITORS IN MULTIPLE MYELOMA CELLS. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1799

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

Chicago Manual of Style (16th Edition):

Youssefian, Leena. “THE SMALL MOLECULE BCL-2 INHIBITOR HA14-1 POTENTIATES THE LETHALITY OF A REGIMEN COMBINING MEK1/2 AND CHK1 INHIBITORS IN MULTIPLE MYELOMA CELLS.” 2009. Thesis, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/1799.

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

MLA Handbook (7th Edition):

Youssefian, Leena. “THE SMALL MOLECULE BCL-2 INHIBITOR HA14-1 POTENTIATES THE LETHALITY OF A REGIMEN COMBINING MEK1/2 AND CHK1 INHIBITORS IN MULTIPLE MYELOMA CELLS.” 2009. Web. 21 Nov 2019.

Vancouver:

Youssefian L. THE SMALL MOLECULE BCL-2 INHIBITOR HA14-1 POTENTIATES THE LETHALITY OF A REGIMEN COMBINING MEK1/2 AND CHK1 INHIBITORS IN MULTIPLE MYELOMA CELLS. [Internet] [Thesis]. Virginia Commonwealth University; 2009. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/1799.

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

Council of Science Editors:

Youssefian L. THE SMALL MOLECULE BCL-2 INHIBITOR HA14-1 POTENTIATES THE LETHALITY OF A REGIMEN COMBINING MEK1/2 AND CHK1 INHIBITORS IN MULTIPLE MYELOMA CELLS. [Thesis]. Virginia Commonwealth University; 2009. Available from: https://scholarscompass.vcu.edu/etd/1799

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


Virginia Commonwealth University

9. Robertson, Chadia L. Analysis of the Role of Astrocyte Elevated Gene-1 in Normal Liver Physiology and in the Onset and Progression of Hepatocellular Carcinoma.

Degree: PhD, Biochemistry, 2014, Virginia Commonwealth University

  First identified over a decade ago, Astrocyte Elevated Gene-1 (AEG-1) has been studied extensively due to early reports of its overexpression in various cancer… (more)

Subjects/Keywords: AEG-1; HCC; NF-κB; LXR; PPARα; Lipid Metabolism; Biochemical Phenomena, Metabolism, and Nutrition; Disease Modeling; Gastroenterology; Genetic Phenomena; Genetic Processes; Hepatology; Immune System Diseases; Medical Immunology; Medical Molecular Biology; Oncology

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APA (6th Edition):

Robertson, C. L. (2014). Analysis of the Role of Astrocyte Elevated Gene-1 in Normal Liver Physiology and in the Onset and Progression of Hepatocellular Carcinoma. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3573

Chicago Manual of Style (16th Edition):

Robertson, Chadia L. “Analysis of the Role of Astrocyte Elevated Gene-1 in Normal Liver Physiology and in the Onset and Progression of Hepatocellular Carcinoma.” 2014. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/3573.

MLA Handbook (7th Edition):

Robertson, Chadia L. “Analysis of the Role of Astrocyte Elevated Gene-1 in Normal Liver Physiology and in the Onset and Progression of Hepatocellular Carcinoma.” 2014. Web. 21 Nov 2019.

Vancouver:

Robertson CL. Analysis of the Role of Astrocyte Elevated Gene-1 in Normal Liver Physiology and in the Onset and Progression of Hepatocellular Carcinoma. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2014. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/3573.

Council of Science Editors:

Robertson CL. Analysis of the Role of Astrocyte Elevated Gene-1 in Normal Liver Physiology and in the Onset and Progression of Hepatocellular Carcinoma. [Doctoral Dissertation]. Virginia Commonwealth University; 2014. Available from: https://scholarscompass.vcu.edu/etd/3573


Virginia Commonwealth University

10. Subramanian, Preeti. Role of Ceramide-1-Phosphate as a Specific and Potent Activator of Group IVA Cytosolic Phospholipase A2 Alpha.

Degree: PhD, Biochemistry, 2007, Virginia Commonwealth University

 Eicosanoids are potent mediators of inflammatory response whose role has been well established in inflammatory disorders. Release of arachidonic acid by group IVA cytosolic phospholipase… (more)

Subjects/Keywords: Cytosolic phospholipase A2; Inflammation; Mixed micelle assay; Translocation; Eicosanoids; Ceramide-1-phosphate; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Subramanian, P. (2007). Role of Ceramide-1-Phosphate as a Specific and Potent Activator of Group IVA Cytosolic Phospholipase A2 Alpha. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/745

Chicago Manual of Style (16th Edition):

Subramanian, Preeti. “Role of Ceramide-1-Phosphate as a Specific and Potent Activator of Group IVA Cytosolic Phospholipase A2 Alpha.” 2007. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/745.

MLA Handbook (7th Edition):

Subramanian, Preeti. “Role of Ceramide-1-Phosphate as a Specific and Potent Activator of Group IVA Cytosolic Phospholipase A2 Alpha.” 2007. Web. 21 Nov 2019.

Vancouver:

Subramanian P. Role of Ceramide-1-Phosphate as a Specific and Potent Activator of Group IVA Cytosolic Phospholipase A2 Alpha. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2007. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/745.

Council of Science Editors:

Subramanian P. Role of Ceramide-1-Phosphate as a Specific and Potent Activator of Group IVA Cytosolic Phospholipase A2 Alpha. [Doctoral Dissertation]. Virginia Commonwealth University; 2007. Available from: https://scholarscompass.vcu.edu/etd/745


Virginia Commonwealth University

11. Strub, Graham Michael. INTRACELLULAR TARGETS OF SPHINGOSINE-1-PHOSPHATE.

Degree: PhD, Biochemistry, 2009, Virginia Commonwealth University

 The bioactive lipid mediator sphingosine-1-phosphate (S1P) has emerged as a key regulator of a variety of important physiological functions, including cell growth, cell survival, cell… (more)

Subjects/Keywords: Sphingosine-1-phosphate; Sphingosine kinase; sphingolipid metabolites; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Strub, G. M. (2009). INTRACELLULAR TARGETS OF SPHINGOSINE-1-PHOSPHATE. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5

Chicago Manual of Style (16th Edition):

Strub, Graham Michael. “INTRACELLULAR TARGETS OF SPHINGOSINE-1-PHOSPHATE.” 2009. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/5.

MLA Handbook (7th Edition):

Strub, Graham Michael. “INTRACELLULAR TARGETS OF SPHINGOSINE-1-PHOSPHATE.” 2009. Web. 21 Nov 2019.

Vancouver:

Strub GM. INTRACELLULAR TARGETS OF SPHINGOSINE-1-PHOSPHATE. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2009. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/5.

Council of Science Editors:

Strub GM. INTRACELLULAR TARGETS OF SPHINGOSINE-1-PHOSPHATE. [Doctoral Dissertation]. Virginia Commonwealth University; 2009. Available from: https://scholarscompass.vcu.edu/etd/5


Virginia Commonwealth University

12. Wijesinghe, Dayanjan. Ceramide Kinase and Ceramide-1-Phosphate.

Degree: PhD, Biochemistry, 2008, Virginia Commonwealth University

 Ceramide-1-phosphate (C1P) is a bioactive lipid that has been implicated in many biological processes. Our laboratory has conclusively demonstrated its role in inflammation via activation… (more)

Subjects/Keywords: Inflammation; ceramide-1-phosphate; ceramide kinase; cytosolic phospholipase A2; arachidonic acid; lipidomics; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Wijesinghe, D. (2008). Ceramide Kinase and Ceramide-1-Phosphate. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1621

Chicago Manual of Style (16th Edition):

Wijesinghe, Dayanjan. “Ceramide Kinase and Ceramide-1-Phosphate.” 2008. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/1621.

MLA Handbook (7th Edition):

Wijesinghe, Dayanjan. “Ceramide Kinase and Ceramide-1-Phosphate.” 2008. Web. 21 Nov 2019.

Vancouver:

Wijesinghe D. Ceramide Kinase and Ceramide-1-Phosphate. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2008. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/1621.

Council of Science Editors:

Wijesinghe D. Ceramide Kinase and Ceramide-1-Phosphate. [Doctoral Dissertation]. Virginia Commonwealth University; 2008. Available from: https://scholarscompass.vcu.edu/etd/1621

13. Seashols, Sarah. Variation and Modulation of microRNAs in Prostate Cancer and Biological Fluids.

Degree: PhD, Biochemistry, 2013, Virginia Commonwealth University

 Prostate cancer is the second-most diagnosed and fatal carcinoma for males in the United States, and better diagnostic markers and potential therapies are needed. microRNAs… (more)

Subjects/Keywords: microRNA; prostate cancer; forensic body fluid identification; c-KIT; AATF/Che-1; e-cadherin; SOCS5; Biochemistry, Biophysics, and Structural Biology; Life Sciences

5 Figure 1-2: Biogenesis of microRNAs… …Figure 1-5: miR-17-3p directly binds and modulates vimentin, an intermediate filament key to… …Figure 5-1: miR-9 levels are upregulated in all prostate cancer cell line models. ..... 120… …113 Table 5-1: Proven direct targets of miR-9… …Suppressor of cytokine signalling 5 SOS Son of Sevenless protein Sp1 specificity protein 1… 

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APA (6th Edition):

Seashols, S. (2013). Variation and Modulation of microRNAs in Prostate Cancer and Biological Fluids. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3258

Chicago Manual of Style (16th Edition):

Seashols, Sarah. “Variation and Modulation of microRNAs in Prostate Cancer and Biological Fluids.” 2013. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 21, 2019. https://scholarscompass.vcu.edu/etd/3258.

MLA Handbook (7th Edition):

Seashols, Sarah. “Variation and Modulation of microRNAs in Prostate Cancer and Biological Fluids.” 2013. Web. 21 Nov 2019.

Vancouver:

Seashols S. Variation and Modulation of microRNAs in Prostate Cancer and Biological Fluids. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2013. [cited 2019 Nov 21]. Available from: https://scholarscompass.vcu.edu/etd/3258.

Council of Science Editors:

Seashols S. Variation and Modulation of microRNAs in Prostate Cancer and Biological Fluids. [Doctoral Dissertation]. Virginia Commonwealth University; 2013. Available from: https://scholarscompass.vcu.edu/etd/3258

.