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You searched for +publisher:"University of Alabama – Birmingham" +contributor:("Bailey, Shannon M.<br>"). Showing records 1 – 8 of 8 total matches.

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1. Filiano, Anthony J. The protective role of transglutaminase 2 in ischemic stroke.

Degree: PhD, 2009, University of Alabama – Birmingham

Stroke is a leading cause of long term disabilities in the US. Currently, administration of thrombolytics is the only approved therapy. Due to the variability,… (more)

Subjects/Keywords: Aryl Hydrocarbon Receptor Nuclear Translocator  – metabolism<; br>; Cell Hypoxia<; br>; GTP-Binding Proteins  – metabolism<; br>; Ischemia  – prevention & control<; br>; Neurons  – metabolism<; br>; Transglutaminases  – metabolism

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

APA (6th Edition):

Filiano, A. J. (2009). The protective role of transglutaminase 2 in ischemic stroke. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,496

Chicago Manual of Style (16th Edition):

Filiano, Anthony J. “The protective role of transglutaminase 2 in ischemic stroke.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,496.

MLA Handbook (7th Edition):

Filiano, Anthony J. “The protective role of transglutaminase 2 in ischemic stroke.” 2009. Web. 16 Jul 2019.

Vancouver:

Filiano AJ. The protective role of transglutaminase 2 in ischemic stroke. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,496.

Council of Science Editors:

Filiano AJ. The protective role of transglutaminase 2 in ischemic stroke. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,496

2. Floyd, Kyle Anthony. Distribution/localization And Relative Quantitation Of C-Terminal αa-Crystallin Truncation Products Within Lenses Of Icr/f Rats Treated With Dietary Supplemented Genistein.

Degree: 2012, University of Alabama – Birmingham

The ocular lens functions to focus light coming into the eye onto the retina. Lens development begins in utero, and continues over an individual's lifetime.… (more)

Subjects/Keywords: alpha-Crystallin A Chain – metabolism.<; br>; Cataract – chemically induced.<; br>; Cataract – physiopathology<; br>; Dietary Supplements – toxicity.<; br>; Genistein – toxicity.<; br>; Lens, Crystalline – drug effects.<; br>; Public Health

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APA (6th Edition):

Floyd, K. A. (2012). Distribution/localization And Relative Quantitation Of C-Terminal αa-Crystallin Truncation Products Within Lenses Of Icr/f Rats Treated With Dietary Supplemented Genistein. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1808

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):

Floyd, Kyle Anthony. “Distribution/localization And Relative Quantitation Of C-Terminal αa-Crystallin Truncation Products Within Lenses Of Icr/f Rats Treated With Dietary Supplemented Genistein.” 2012. Thesis, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1808.

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

MLA Handbook (7th Edition):

Floyd, Kyle Anthony. “Distribution/localization And Relative Quantitation Of C-Terminal αa-Crystallin Truncation Products Within Lenses Of Icr/f Rats Treated With Dietary Supplemented Genistein.” 2012. Web. 16 Jul 2019.

Vancouver:

Floyd KA. Distribution/localization And Relative Quantitation Of C-Terminal αa-Crystallin Truncation Products Within Lenses Of Icr/f Rats Treated With Dietary Supplemented Genistein. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1808.

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

Council of Science Editors:

Floyd KA. Distribution/localization And Relative Quantitation Of C-Terminal αa-Crystallin Truncation Products Within Lenses Of Icr/f Rats Treated With Dietary Supplemented Genistein. [Thesis]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1808

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

3. Jones, Page. Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model.

Degree: PhD, 2008, University of Alabama – Birmingham

Mutations to copper,zinc superoxide dismutase (Cu,Zn SOD or SOD1) are the only known causes of amyotrophic lateral sclerosis (ALS), a neurodegenerative disorder characterized primarily by… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis  – enzymology <; br>; Copper  – metabolism <; br>; Disease Progression <; br>; Nerve Degeneration  – enzymology <; br>; Neurons  – metabolism <; br>; Spinal Cord  – enzymology <; br>; Superoxide Dismutase  – metabolism

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APA (6th Edition):

Jones, P. (2008). Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,370

Chicago Manual of Style (16th Edition):

Jones, Page. “Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,370.

MLA Handbook (7th Edition):

Jones, Page. “Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model.” 2008. Web. 16 Jul 2019.

Vancouver:

Jones P. Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,370.

Council of Science Editors:

Jones P. Enzymatic and proteomic analysis of spinal cord in a G93A ALS mouse model. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,370

4. Jumbo Lucioni, Patricia P. A system genetics analysis of energy metabolism traits in Drosophila melanogaster.

Degree: PhD, 2009, University of Alabama – Birmingham

Obesity is emerging as a global public health problem and it has shown to precede and predict the development of type 2 diabetes, a complex… (more)

Subjects/Keywords: Drosophila melanogaster  – genetics<; br>; Energy Metabolism<; br>; Mitochondria  – metabolism<; br>; Obesity  – genetics<; br>; Obesity  – complications

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APA (6th Edition):

Jumbo Lucioni, P. P. (2009). A system genetics analysis of energy metabolism traits in Drosophila melanogaster. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,568

Chicago Manual of Style (16th Edition):

Jumbo Lucioni, Patricia P. “A system genetics analysis of energy metabolism traits in Drosophila melanogaster.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,568.

MLA Handbook (7th Edition):

Jumbo Lucioni, Patricia P. “A system genetics analysis of energy metabolism traits in Drosophila melanogaster.” 2009. Web. 16 Jul 2019.

Vancouver:

Jumbo Lucioni PP. A system genetics analysis of energy metabolism traits in Drosophila melanogaster. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,568.

Council of Science Editors:

Jumbo Lucioni PP. A system genetics analysis of energy metabolism traits in Drosophila melanogaster. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,568

5. Oh, JooYeun. The modification of cell signaling proteins by reactive prostaglandins in endothelial cells.

Degree: PhD, 2008, University of Alabama – Birmingham

The cyclooxygenase (COX) pathway generates reactive prostaglandins lipid, which form covalent protein adducts that modulate cell signaling pathways. It has been shown that covalent modification… (more)

Subjects/Keywords: Antioxidants  – metabolism<; br>; Atherosclerosis<; br>; Biochemistry  – methods<; br>; Intracellular Signaling Peptides and Proteins  – metabolism<; br>; Prostaglandin D2  – analogs & derivatives<; br>; Proteins  – analysis<; br>; Proteomics  – methods<; br>; Sulfhydryl Compounds  – analysis

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APA (6th Edition):

Oh, J. (2008). The modification of cell signaling proteins by reactive prostaglandins in endothelial cells. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,686

Chicago Manual of Style (16th Edition):

Oh, JooYeun. “The modification of cell signaling proteins by reactive prostaglandins in endothelial cells.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,686.

MLA Handbook (7th Edition):

Oh, JooYeun. “The modification of cell signaling proteins by reactive prostaglandins in endothelial cells.” 2008. Web. 16 Jul 2019.

Vancouver:

Oh J. The modification of cell signaling proteins by reactive prostaglandins in endothelial cells. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,686.

Council of Science Editors:

Oh J. The modification of cell signaling proteins by reactive prostaglandins in endothelial cells. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,686

6. Salman, Emily Deanna. Human cytosolic sulfotransferase 2B1b: structure, function, and expression in human brain.

Degree: PhD, 2011, University of Alabama – Birmingham

The human cytosolic sulfotransferases are a family of phase II drug-metabolizing enzymes that conjugate a sulfonate moiety from 3’-phosphoadenosine 5’-phosphosulfate (PAPS) to a hydroxyl moeity… (more)

Subjects/Keywords: Arylsulfotransferase  – metabolism<; br>; Brain  – enzymology<; br>; Cytosol  – enzymology<; br>; Immunohistochemistry<; br>; Sulfotransferases  – metabolism

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APA (6th Edition):

Salman, E. D. (2011). Human cytosolic sulfotransferase 2B1b: structure, function, and expression in human brain. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,960

Chicago Manual of Style (16th Edition):

Salman, Emily Deanna. “Human cytosolic sulfotransferase 2B1b: structure, function, and expression in human brain.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,960.

MLA Handbook (7th Edition):

Salman, Emily Deanna. “Human cytosolic sulfotransferase 2B1b: structure, function, and expression in human brain.” 2011. Web. 16 Jul 2019.

Vancouver:

Salman ED. Human cytosolic sulfotransferase 2B1b: structure, function, and expression in human brain. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,960.

Council of Science Editors:

Salman ED. Human cytosolic sulfotransferase 2B1b: structure, function, and expression in human brain. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,960

7. Wright, Marcienne M. Regulation of the human heme oxygenase-1 gene by nitro-linoleic acid.

Degree: PhD, 2009, University of Alabama – Birmingham

Nitro-fatty acids (NO-FA) exert anti-inflammatory effects in the vasculature. Heme oxygenase-1 (HO-1) degrades heme into iron, biliverdin, and carbon monoxide and is up-regulated as an… (more)

Subjects/Keywords: Cyclic AMP  – physiology<; br>; E-Box Elements  – physiology<; br>; Heme Oxygenase-1  – biosynthesis<; br>; Linoleic Acids  – metabolism<; br>; Nitro Compounds  – metabolism<; br>; Transcription Factor AP-1  – physiology

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APA (6th Edition):

Wright, M. M. (2009). Regulation of the human heme oxygenase-1 gene by nitro-linoleic acid. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1010

Chicago Manual of Style (16th Edition):

Wright, Marcienne M. “Regulation of the human heme oxygenase-1 gene by nitro-linoleic acid.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1010.

MLA Handbook (7th Edition):

Wright, Marcienne M. “Regulation of the human heme oxygenase-1 gene by nitro-linoleic acid.” 2009. Web. 16 Jul 2019.

Vancouver:

Wright MM. Regulation of the human heme oxygenase-1 gene by nitro-linoleic acid. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1010.

Council of Science Editors:

Wright MM. Regulation of the human heme oxygenase-1 gene by nitro-linoleic acid. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1010

8. Stein, Asaf. The Hypometabolic Actions Of Hydrogen Sulfide In Mammalian Systems.

Degree: PhD, 2012, University of Alabama – Birmingham

In recent years, hydrogen sulfide (H2S) has been identified as a ubiquitous cell signaling molecule. In addition to its diverse physiological roles, H2S has emerged… (more)

Subjects/Keywords: Anoxia – metabolism. Hydrogen Sulfide – administration & dosage. Myocardium – metabolism Oxygen – metabolism Signal Transduction – drug effects Thiosulfate Sulfurtransferase.

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APA (6th Edition):

Stein, A. (2012). The Hypometabolic Actions Of Hydrogen Sulfide In Mammalian Systems. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1641

Chicago Manual of Style (16th Edition):

Stein, Asaf. “The Hypometabolic Actions Of Hydrogen Sulfide In Mammalian Systems.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed July 16, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1641.

MLA Handbook (7th Edition):

Stein, Asaf. “The Hypometabolic Actions Of Hydrogen Sulfide In Mammalian Systems.” 2012. Web. 16 Jul 2019.

Vancouver:

Stein A. The Hypometabolic Actions Of Hydrogen Sulfide In Mammalian Systems. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Jul 16]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1641.

Council of Science Editors:

Stein A. The Hypometabolic Actions Of Hydrogen Sulfide In Mammalian Systems. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1641

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