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Level: doctoral  Dates: 2010 – 2014

You searched for subject:( GTPase Activating Proteins metabolism 60). Showing records 1 – 30 of 2848 total matches.

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1. Funk, Adam J. Intracellular signaling abnormalities in schizophrenia.

Degree: PhD, 2011, University of Alabama – Birmingham

The pathophysiology of schizophrenia is complex and diverse, with many classes of receptors, neurotransmitters, and brain regions implicated in this illness. The many hypotheses proposed… (more)

Subjects/Keywords: Carrier Proteins  – metabolism<; br>; GTPase-Activating Proteins  – metabolism<; br>; Gyrus Cinguli  – metabolism<; br>; Intracellular Signaling Peptides and Proteins  – metabolism<; br>; Membrane Proteins  – metabolism<; br>; Prefrontal Cortex  – metabolism<; br>; Schizophrenia  – metabolism

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APA (6th Edition):

Funk, A. J. (2011). Intracellular signaling abnormalities in schizophrenia. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1151

Chicago Manual of Style (16th Edition):

Funk, Adam J. “Intracellular signaling abnormalities in schizophrenia.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1151.

MLA Handbook (7th Edition):

Funk, Adam J. “Intracellular signaling abnormalities in schizophrenia.” 2011. Web. 14 Dec 2019.

Vancouver:

Funk AJ. Intracellular signaling abnormalities in schizophrenia. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1151.

Council of Science Editors:

Funk AJ. Intracellular signaling abnormalities in schizophrenia. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1151

2. Lowery, Jason. Regulation Of Membrane Traffic By The Big2 Member Of Guanine Nucleotide Exchange Factors.

Degree: PhD, 2012, University of Alabama – Birmingham

Vesicular transport is an essential cellular process that facilitates the movement of molecules within a cell. The importance of vesicular transport is highlighted by numerous… (more)

Subjects/Keywords: ADP-Ribosylation Factors – chemistry.<; br>; GTPase-Activating Proteins – chemistry.<; br>; Guanine Nucleotide Exchange Factors – chemistry.<; br>; Guanosine Diphosphate – chemistry.<; br>; Guanosine Triphosphate – chemistry.<; br>; Protein Structure, Tertiary

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APA (6th Edition):

Lowery, J. (2012). Regulation Of Membrane Traffic By The Big2 Member Of Guanine Nucleotide Exchange Factors. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1432

Chicago Manual of Style (16th Edition):

Lowery, Jason. “Regulation Of Membrane Traffic By The Big2 Member Of Guanine Nucleotide Exchange Factors.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1432.

MLA Handbook (7th Edition):

Lowery, Jason. “Regulation Of Membrane Traffic By The Big2 Member Of Guanine Nucleotide Exchange Factors.” 2012. Web. 14 Dec 2019.

Vancouver:

Lowery J. Regulation Of Membrane Traffic By The Big2 Member Of Guanine Nucleotide Exchange Factors. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1432.

Council of Science Editors:

Lowery J. Regulation Of Membrane Traffic By The Big2 Member Of Guanine Nucleotide Exchange Factors. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1432

3. Beagle, Brandon Richard. Canonical Wnt signaling by the proteolytic processing of LRP6.

Degree: PhD, 2010, University of Alabama – Birmingham

Low density Lipoprotein receptor Related 6 (LRP6) functions as an essential coreceptor for Wnt/β-catenin signaling as pathway activation, reflected by cytosolic β- catenin stabilization and… (more)

Subjects/Keywords: beta Catenin  – metabolism<; br>; Glycogen Synthase Kinase 3  – metabolism<; br>; LDL-Receptor Related Proteins  – metabolism<; br>; Lymphoid Enhancer-Binding Factor 1  – metabolism<; br>; Repressor Proteins  – metabolism<; br>; Transcription Factors  – metabolism<; br>; Wnt Proteins  – metabolism

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APA (6th Edition):

Beagle, B. R. (2010). Canonical Wnt signaling by the proteolytic processing of LRP6. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,857

Chicago Manual of Style (16th Edition):

Beagle, Brandon Richard. “Canonical Wnt signaling by the proteolytic processing of LRP6.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,857.

MLA Handbook (7th Edition):

Beagle, Brandon Richard. “Canonical Wnt signaling by the proteolytic processing of LRP6.” 2010. Web. 14 Dec 2019.

Vancouver:

Beagle BR. Canonical Wnt signaling by the proteolytic processing of LRP6. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,857.

Council of Science Editors:

Beagle BR. Canonical Wnt signaling by the proteolytic processing of LRP6. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,857

4. Cui, Wenjun. Structural and mechanistic studies on ER UPR sensor PERK and mitochondrial translocon element TIM44.

Degree: PhD, 2010, University of Alabama – Birmingham

The unfolded protein response is one mechanism utilized by endoplasmic reticulum (ER) to maintain the homeostasis between ER protein folding machinery and ER proteins. UPR… (more)

Subjects/Keywords: Mitochondrial Membrane Transport Proteins  – chemistry<; br>; Mitochondrial Membrane Transport Proteins  – metabolism<; br>; Mitochondrial Membranes  – metabolism<; br>; Saccharomyces cerevisiae  – metabolism<; br>; Saccharomyces cerevisiae Proteins  – chemistry<; br>; Saccharomyces cerevisiae Proteins  – metabolism<; br>; Unfolded Protein Response

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APA (6th Edition):

Cui, W. (2010). Structural and mechanistic studies on ER UPR sensor PERK and mitochondrial translocon element TIM44. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1088

Chicago Manual of Style (16th Edition):

Cui, Wenjun. “Structural and mechanistic studies on ER UPR sensor PERK and mitochondrial translocon element TIM44.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1088.

MLA Handbook (7th Edition):

Cui, Wenjun. “Structural and mechanistic studies on ER UPR sensor PERK and mitochondrial translocon element TIM44.” 2010. Web. 14 Dec 2019.

Vancouver:

Cui W. Structural and mechanistic studies on ER UPR sensor PERK and mitochondrial translocon element TIM44. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1088.

Council of Science Editors:

Cui W. Structural and mechanistic studies on ER UPR sensor PERK and mitochondrial translocon element TIM44. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1088

5. Indran, Sabarish Vellatheri. Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions.

Degree: PhD, 2010, University of Alabama – Birmingham

Human cytomegalovirus, a ubiquitous human pathogen, establishes a persistent infection in the infected host. HCMV assembly takes place in the nucleus and cytoplasm of infected… (more)

Subjects/Keywords: Adaptor Proteins, Signal Transducing – physiology.<; br>; Cytomegalovirus<; br>; Cytoskeletal Proteins – physiology<; br>; Host-Pathogen Interactions.<; br>; Phosphoproteins – metabolism<; br>; Viral Matrix Proteins – metabolism.<; br>; Virus Assembly.<; br>; rab GTP-Binding Proteins – metabolism.

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APA (6th Edition):

Indran, S. V. (2010). Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1351

Chicago Manual of Style (16th Edition):

Indran, Sabarish Vellatheri. “Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1351.

MLA Handbook (7th Edition):

Indran, Sabarish Vellatheri. “Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions.” 2010. Web. 14 Dec 2019.

Vancouver:

Indran SV. Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1351.

Council of Science Editors:

Indran SV. Role of the human cytomegalovirus tegument protein pp150 in the trafficking and assembly of infectious virions. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1351

6. Balasubramani, Anand. Evolutionarily Conserved Cis-Acting Elements Regulate Lineage-Specific Expression Of Ifng.

Degree: PhD, 2010, University of Alabama – Birmingham

The ability to differentially manipulate available genetic information in order to generate diverse cellular identities represents an innovation of complex multicellular eukaryotic organisms. Cis-acting modules… (more)

Subjects/Keywords: DNA Replication – physiology.<; br>; Drosophila – metabolism.<; br>; Drosophila Proteins – metabolism.<; br>; GTP Phosphohydrolases – metabolism.<; br>; Microfilament Proteins – metabolism.<; br>; Multiprotein Complexes – metabolism.<; br>; Origin Recognition Complex – metabolism.

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APA (6th Edition):

Balasubramani, A. (2010). Evolutionarily Conserved Cis-Acting Elements Regulate Lineage-Specific Expression Of Ifng. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1428

Chicago Manual of Style (16th Edition):

Balasubramani, Anand. “Evolutionarily Conserved Cis-Acting Elements Regulate Lineage-Specific Expression Of Ifng.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1428.

MLA Handbook (7th Edition):

Balasubramani, Anand. “Evolutionarily Conserved Cis-Acting Elements Regulate Lineage-Specific Expression Of Ifng.” 2010. Web. 14 Dec 2019.

Vancouver:

Balasubramani A. Evolutionarily Conserved Cis-Acting Elements Regulate Lineage-Specific Expression Of Ifng. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1428.

Council of Science Editors:

Balasubramani A. Evolutionarily Conserved Cis-Acting Elements Regulate Lineage-Specific Expression Of Ifng. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1428

7. Masyukova, Svetlana V. Analysis of NPHP complex genetic interactions associated with human cilia disorders.

Degree: PhD, 2011, University of Alabama – Birmingham

Primary cilia are antenna-like organelles that extend from the surface of almost all mammalian cell types. They regulate many signaling pathways and sense physical and… (more)

Subjects/Keywords: Caenorhabditis elegans Proteins – metabolism.<; br>; Cilia – metabolism.<; br>; Membrane Proteins – metabolism<; br>; Mutation, Missense – physiology.<; br>; Proteins – genetics<; br>; Proteins – metabolism

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APA (6th Edition):

Masyukova, S. V. (2011). Analysis of NPHP complex genetic interactions associated with human cilia disorders. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1352

Chicago Manual of Style (16th Edition):

Masyukova, Svetlana V. “Analysis of NPHP complex genetic interactions associated with human cilia disorders.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1352.

MLA Handbook (7th Edition):

Masyukova, Svetlana V. “Analysis of NPHP complex genetic interactions associated with human cilia disorders.” 2011. Web. 14 Dec 2019.

Vancouver:

Masyukova SV. Analysis of NPHP complex genetic interactions associated with human cilia disorders. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1352.

Council of Science Editors:

Masyukova SV. Analysis of NPHP complex genetic interactions associated with human cilia disorders. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1352

8. Mans, Keri April. Translocation and function of Akt in the mitochondria.

Degree: PhD, 2010, University of Alabama – Birmingham

The ubiquitously expressed kinase Akt is a known survival protein, and is involved in multiple cell signaling cascades, notably the phosphatidylinositol 3-kinase (PI3K) pathway. Active… (more)

Subjects/Keywords: HSP90 Heat-Shock Proteins  – metabolism<; br>; Mitochondria  – metabolism<; br>; Oncogene Protein v-akt  – metabolism<; br>; Phosphatidylinositol 3-Kinase<; br>; Postmortem Changes

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APA (6th Edition):

Mans, K. A. (2010). Translocation and function of Akt in the mitochondria. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,831

Chicago Manual of Style (16th Edition):

Mans, Keri April. “Translocation and function of Akt in the mitochondria.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,831.

MLA Handbook (7th Edition):

Mans, Keri April. “Translocation and function of Akt in the mitochondria.” 2010. Web. 14 Dec 2019.

Vancouver:

Mans KA. Translocation and function of Akt in the mitochondria. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,831.

Council of Science Editors:

Mans KA. Translocation and function of Akt in the mitochondria. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,831

9. Dolan, Philip J. The role of post-translational modifications and valosin-containing protein in the turnover and stability of the microtubule-associated protein tau.

Degree: PhD, 2010, University of Alabama – Birmingham

Alzheimer Disease (AD) is pathologically characterized by the appearance of senile plaques composed of β-amyloid (Aβ) and neurofibrillary tangles composed of the microtubule-associated protein tau.… (more)

Subjects/Keywords: Alzheimer Disease  – enzymology<; br>; Autophagy<; br>; Caspases  – metabolism<; br>; Protein Kinases  – metabolism<; br>; Signal Transduction<; br>; tau Proteins  – physiology

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APA (6th Edition):

Dolan, P. J. (2010). The role of post-translational modifications and valosin-containing protein in the turnover and stability of the microtubule-associated protein tau. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1090

Chicago Manual of Style (16th Edition):

Dolan, Philip J. “The role of post-translational modifications and valosin-containing protein in the turnover and stability of the microtubule-associated protein tau.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1090.

MLA Handbook (7th Edition):

Dolan, Philip J. “The role of post-translational modifications and valosin-containing protein in the turnover and stability of the microtubule-associated protein tau.” 2010. Web. 14 Dec 2019.

Vancouver:

Dolan PJ. The role of post-translational modifications and valosin-containing protein in the turnover and stability of the microtubule-associated protein tau. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1090.

Council of Science Editors:

Dolan PJ. The role of post-translational modifications and valosin-containing protein in the turnover and stability of the microtubule-associated protein tau. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1090

10. Carter, Robert J. (Robert Joseph). HPV DNA partitioning during mitosis as followed by fluorescence microscopy.

Degree: PhD, 2010, University of Alabama – Birmingham

Human papillomaviruses (HPVs) are small, double-stranded deoxyribonucleic acid (DNA) tumor viruses capable of establishing persistent infections in the epithelia. After infecting actively-dividing basal cells, the… (more)

Subjects/Keywords: DNA-Binding Proteins<; br>; DNA, Viral  – metabolism<; br>; Microscopy, Fluorescence<; br>; Mitosis<; br>; Papillomaviridae  – metabolism<; br>; Plasmids

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APA (6th Edition):

Carter, R. J. (. J. (2010). HPV DNA partitioning during mitosis as followed by fluorescence microscopy. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1253

Chicago Manual of Style (16th Edition):

Carter, Robert J (Robert Joseph). “HPV DNA partitioning during mitosis as followed by fluorescence microscopy.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1253.

MLA Handbook (7th Edition):

Carter, Robert J (Robert Joseph). “HPV DNA partitioning during mitosis as followed by fluorescence microscopy.” 2010. Web. 14 Dec 2019.

Vancouver:

Carter RJ(J. HPV DNA partitioning during mitosis as followed by fluorescence microscopy. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1253.

Council of Science Editors:

Carter RJ(J. HPV DNA partitioning during mitosis as followed by fluorescence microscopy. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1253

11. Genovese, Nicholas J. The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium.

Degree: PhD, 2010, University of Alabama – Birmingham

Though human papillomavirus infection of the human epidermis is epidemiologically widespread and typically benign, manipulation of the cell cycle within host tissues during infections can… (more)

Subjects/Keywords: Cell Cycle<; br>; Cell Transformation, Viral<; br>; Human papillomavirus 16  – metabolism<; br>; Keratinocytes<; br>; Oncogene Proteins, Viral  – metabolism<; br>; Papillomaviridae  – physiology<; br>; Papillomavirus E7 Proteins  – metabolism<; br>; Receptors, Estrogen  – metabolism<; br>; Retinoblastoma-Like Protein p130  – metabolism<; br>; S Phase

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APA (6th Edition):

Genovese, N. J. (2010). The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1158

Chicago Manual of Style (16th Edition):

Genovese, Nicholas J. “The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1158.

MLA Handbook (7th Edition):

Genovese, Nicholas J. “The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium.” 2010. Web. 14 Dec 2019.

Vancouver:

Genovese NJ. The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1158.

Council of Science Editors:

Genovese NJ. The mechanism of human papillomavirus E7 protein mediated S-phase reentry in the squamous epithelium. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1158

12. Hertz, Marla (Marla Ilene). In vivo analysis of the natural diversity of the IGR IRES family and characterizaton of the role of ribosomal protein S25 in IRES-mediated translation.

Degree: PhD, 2011, University of Alabama – Birmingham

Translation of the majority of eukaryotic mRNAs is initiated upon recognition of its 5′ cap structure by translation initiation factors in so-called cap-dependent translation. Capdependent… (more)

Subjects/Keywords: Dicistroviridae  – metabolism<; br>; Gene Expression Regulation<; br>; Hepacivirus  – metabolism<; br>; Prostatic Neoplasms<; br>; Protein Biosynthesis<; br>; Ribosomal Proteins  – metabolism<; br>; Saccharomyces cerevisiae Proteins  – metabolism

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APA (6th Edition):

Hertz, M. (. I. (2011). In vivo analysis of the natural diversity of the IGR IRES family and characterizaton of the role of ribosomal protein S25 in IRES-mediated translation. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,953

Chicago Manual of Style (16th Edition):

Hertz, Marla (Marla Ilene). “In vivo analysis of the natural diversity of the IGR IRES family and characterizaton of the role of ribosomal protein S25 in IRES-mediated translation.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,953.

MLA Handbook (7th Edition):

Hertz, Marla (Marla Ilene). “In vivo analysis of the natural diversity of the IGR IRES family and characterizaton of the role of ribosomal protein S25 in IRES-mediated translation.” 2011. Web. 14 Dec 2019.

Vancouver:

Hertz M(I. In vivo analysis of the natural diversity of the IGR IRES family and characterizaton of the role of ribosomal protein S25 in IRES-mediated translation. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,953.

Council of Science Editors:

Hertz M(I. In vivo analysis of the natural diversity of the IGR IRES family and characterizaton of the role of ribosomal protein S25 in IRES-mediated translation. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,953

13. Dong, Shengli. Characterization of the oligosaccharides of B. anthracis exosporium.

Degree: PhD, 2010, University of Alabama – Birmingham

Fatal systemic anthrax is caused by exposure to spores of Bacillus anthracis. The outermost layer of the B. anthracis spore is called the exosporium. It… (more)

Subjects/Keywords: Amino Sugars  – biosynthesis<; br>; Bacillus anthracis  – genetics<; br>; Bacillus anthracis  – metabolism<; br>; Bacterial Proteins  – metabolism<; br>; Carbohydrate Epimerases  – metabolism<; br>; Deoxyglucose  – analogs & derivatives<; br>; Glycoproteins<; br>; Oligosaccharides<; br>; Operon

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APA (6th Edition):

Dong, S. (2010). Characterization of the oligosaccharides of B. anthracis exosporium. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1237

Chicago Manual of Style (16th Edition):

Dong, Shengli. “Characterization of the oligosaccharides of B. anthracis exosporium.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1237.

MLA Handbook (7th Edition):

Dong, Shengli. “Characterization of the oligosaccharides of B. anthracis exosporium.” 2010. Web. 14 Dec 2019.

Vancouver:

Dong S. Characterization of the oligosaccharides of B. anthracis exosporium. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1237.

Council of Science Editors:

Dong S. Characterization of the oligosaccharides of B. anthracis exosporium. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1237

14. Burke, Stephen P. Regulation of apoptosis by Smac, IAPS, and the ubiquitin proteasome system.

Degree: PhD, 2010, University of Alabama – Birmingham

Apoptosis, or programmed cell death, is essential for the development and maintenance of mammalian tissues. Activation of cysteinyl aspartate specific proteases, called caspases, is crucial… (more)

Subjects/Keywords: Apoptosomes  – genetics<; br>; Caspase 3  – metabolism<; br>; Caspase 9  – metabolism<; br>; Inhibitor of Apoptosis Proteins  – metabolism<; br>; Mitochondrial Proteins<; br>; Protein Multimerization  – metabolism

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APA (6th Edition):

Burke, S. P. (2010). Regulation of apoptosis by Smac, IAPS, and the ubiquitin proteasome system. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,818

Chicago Manual of Style (16th Edition):

Burke, Stephen P. “Regulation of apoptosis by Smac, IAPS, and the ubiquitin proteasome system.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,818.

MLA Handbook (7th Edition):

Burke, Stephen P. “Regulation of apoptosis by Smac, IAPS, and the ubiquitin proteasome system.” 2010. Web. 14 Dec 2019.

Vancouver:

Burke SP. Regulation of apoptosis by Smac, IAPS, and the ubiquitin proteasome system. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,818.

Council of Science Editors:

Burke SP. Regulation of apoptosis by Smac, IAPS, and the ubiquitin proteasome system. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,818

15. Khare, Baldeep. Structural analyses of Streptococcus agalactiae sortases.

Degree: PhD, 2011, University of Alabama – Birmingham

Multi-drug resistance in Gram-positive bacteria is a growing and unwavering challenge for twenty-first century medicine. The enzyme sortase, identified just around the turn of the… (more)

Subjects/Keywords: Aminoacyltransferases  – chemistry<; br>; Aminoacyltransferases  – metabolism<; br>; Bacterial Proteins  – chemistry<; br>; Bacterial Proteins  – metabolism<; br>; Cysteine Endopeptidases  – chemistry<; br>; Cysteine Endopeptidases  – metabolism<; br>; Cysteine Proteinase Inhibitors  – chemistry<; br>; Cysteine Proteinase Inhibitors  – metabolism<; br>; Streptococcus agalactiae  – enzymology

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APA (6th Edition):

Khare, B. (2011). Structural analyses of Streptococcus agalactiae sortases. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1160

Chicago Manual of Style (16th Edition):

Khare, Baldeep. “Structural analyses of Streptococcus agalactiae sortases.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1160.

MLA Handbook (7th Edition):

Khare, Baldeep. “Structural analyses of Streptococcus agalactiae sortases.” 2011. Web. 14 Dec 2019.

Vancouver:

Khare B. Structural analyses of Streptococcus agalactiae sortases. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1160.

Council of Science Editors:

Khare B. Structural analyses of Streptococcus agalactiae sortases. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1160

16. Swindall, Amanda F. The Role Of St6gal-I Sialylation In Fas (cd95) Death Receptor Function And Tumorigenesis.

Degree: PhD, 2012, University of Alabama – Birmingham

The golgi glycosyltransferase, ST6Gal-I, adds a negatively-charged sialic acid in an alpha-2-6 linkage to N-linked glycans. ST6Gal-I is upregulated in many cancers, and is associated… (more)

Subjects/Keywords: Antigens, CD – metabolism.<; br>; Antigens, CD95 – metabolism.<; br>; Apoptosis<; br>; Tumor Cells, Cultured<; br>; Colonic Neoplasms<; br>; Neoplasm Proteins – metabolism.<; br>; Sialyltransferases – metabolism.

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APA (6th Edition):

Swindall, A. F. (2012). The Role Of St6gal-I Sialylation In Fas (cd95) Death Receptor Function And Tumorigenesis. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1392

Chicago Manual of Style (16th Edition):

Swindall, Amanda F. “The Role Of St6gal-I Sialylation In Fas (cd95) Death Receptor Function And Tumorigenesis.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1392.

MLA Handbook (7th Edition):

Swindall, Amanda F. “The Role Of St6gal-I Sialylation In Fas (cd95) Death Receptor Function And Tumorigenesis.” 2012. Web. 14 Dec 2019.

Vancouver:

Swindall AF. The Role Of St6gal-I Sialylation In Fas (cd95) Death Receptor Function And Tumorigenesis. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1392.

Council of Science Editors:

Swindall AF. The Role Of St6gal-I Sialylation In Fas (cd95) Death Receptor Function And Tumorigenesis. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1392

17. Stout, Randy Franklin. Calcium dynamics of glial cells and genetic influences on behavior of the nematode Caenorhabditis elegans.

Degree: PhD, 2011, University of Alabama – Birmingham

A major challenge in neuroscience is understanding how the different neural cell types work together to process information and produce a behavioral output. Glial cells… (more)

Subjects/Keywords: Astrocytes  – metabolism<; br>; Caenorhabditis elegans<; br>; Caenorhabditis elegans Proteins  – metabolism<; br>; Calcium Channels, L-Type  – metabolism<; br>; Neuroglia  – metabolism<; br>; Oligodendroglia  – metabolism

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APA (6th Edition):

Stout, R. F. (2011). Calcium dynamics of glial cells and genetic influences on behavior of the nematode Caenorhabditis elegans. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1066

Chicago Manual of Style (16th Edition):

Stout, Randy Franklin. “Calcium dynamics of glial cells and genetic influences on behavior of the nematode Caenorhabditis elegans.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1066.

MLA Handbook (7th Edition):

Stout, Randy Franklin. “Calcium dynamics of glial cells and genetic influences on behavior of the nematode Caenorhabditis elegans.” 2011. Web. 14 Dec 2019.

Vancouver:

Stout RF. Calcium dynamics of glial cells and genetic influences on behavior of the nematode Caenorhabditis elegans. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1066.

Council of Science Editors:

Stout RF. Calcium dynamics of glial cells and genetic influences on behavior of the nematode Caenorhabditis elegans. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1066

18. Cuddapah, Vishnu Anand. Regulation Of Clc-3 In Human Malignant Glioma.

Degree: PhD, 2012, University of Alabama – Birmingham

Malignant gliomas are the most common and deadly form of primary brain cancer afflicting adults. Current treatment regimens, including surgical debulking, radiotherapy, and chemotherapy, have… (more)

Subjects/Keywords: Brain Neoplasms – metabolism<; br>; Calcium-Calmodulin-Dependent Protein Kinase Type 2 – metabolism.<; br>; Cell Movement – physiology<; br>; Chloride Channels – metabolism.<; br>; Gene Expression Regulation<; br>; Gene Expression Regulation, Enzymologic<; br>; Gene Expression Regulation, Neoplastic<; br>; Glioma – metabolism<; br>; Ion Channels – metabolism<; br>; Membrane Transport Proteins – metabolism.<; br>; Mitosis<; br>; Neoplasms – metabolism<; br>; Neoplasms – pathology

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APA (6th Edition):

Cuddapah, V. A. (2012). Regulation Of Clc-3 In Human Malignant Glioma. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1394

Chicago Manual of Style (16th Edition):

Cuddapah, Vishnu Anand. “Regulation Of Clc-3 In Human Malignant Glioma.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1394.

MLA Handbook (7th Edition):

Cuddapah, Vishnu Anand. “Regulation Of Clc-3 In Human Malignant Glioma.” 2012. Web. 14 Dec 2019.

Vancouver:

Cuddapah VA. Regulation Of Clc-3 In Human Malignant Glioma. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1394.

Council of Science Editors:

Cuddapah VA. Regulation Of Clc-3 In Human Malignant Glioma. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1394

19. Asomugha, Chinwe Obioma. Post-translational modifications, structure and functions of human lens crystallins.

Degree: PhD, 2011, University of Alabama – Birmingham

Cataract is an opacification of the lens causing reduction in vision over time. It is one of the leading causes of vision loss among adults… (more)

Subjects/Keywords: alpha-Crystallin A Chain  – chemistry<; br>; alpha-Crystallin B Chain  – chemistry<; br>; Asparagine  – metabolism<; br>; Cell Nucleus  – metabolism<; br>; Crystallins  – metabolism<; br>; Fluorescent Dyes<; br>; Lasers<; br>; Lens, Crystalline  – metabolism<; br>; Microdissection  – methods<; br>; Molecular Chaperones<; br>; Protein Structure, Tertiary  – physiology<; br>; Recombinant Fusion Proteins  – chemistry<; br>; Recombinant Proteins  – metabolism

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APA (6th Edition):

Asomugha, C. O. (2011). Post-translational modifications, structure and functions of human lens crystallins. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1149

Chicago Manual of Style (16th Edition):

Asomugha, Chinwe Obioma. “Post-translational modifications, structure and functions of human lens crystallins.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1149.

MLA Handbook (7th Edition):

Asomugha, Chinwe Obioma. “Post-translational modifications, structure and functions of human lens crystallins.” 2011. Web. 14 Dec 2019.

Vancouver:

Asomugha CO. Post-translational modifications, structure and functions of human lens crystallins. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1149.

Council of Science Editors:

Asomugha CO. Post-translational modifications, structure and functions of human lens crystallins. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1149


University of Manchester

20. Yeung, Ching-Yan. Identification of Arhgap28, a new regulator of stress fibre formation in cells assembling a fibrous extracellular matrix.

Degree: PhD, 2012, University of Manchester

 The motivation for this PhD thesis was to understand the molecular basis of how cells regulate the formation of an organised and mechanically strong extracellular… (more)

Subjects/Keywords: 616.75; tendon; Rho GTPase activating protein; extracellular matrix; Arhgap28; tendon

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APA (6th Edition):

Yeung, C. (2012). Identification of Arhgap28, a new regulator of stress fibre formation in cells assembling a fibrous extracellular matrix. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/identification-of-arhgap28-a-new-regulator-of-stress-fibre-formation-in-cells-assembling-a-fibrous-extracellular-matrix(93164a99-54f1-4719-9eef-b81d3f3bc20e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559313

Chicago Manual of Style (16th Edition):

Yeung, Ching-Yan. “Identification of Arhgap28, a new regulator of stress fibre formation in cells assembling a fibrous extracellular matrix.” 2012. Doctoral Dissertation, University of Manchester. Accessed December 14, 2019. https://www.research.manchester.ac.uk/portal/en/theses/identification-of-arhgap28-a-new-regulator-of-stress-fibre-formation-in-cells-assembling-a-fibrous-extracellular-matrix(93164a99-54f1-4719-9eef-b81d3f3bc20e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559313.

MLA Handbook (7th Edition):

Yeung, Ching-Yan. “Identification of Arhgap28, a new regulator of stress fibre formation in cells assembling a fibrous extracellular matrix.” 2012. Web. 14 Dec 2019.

Vancouver:

Yeung C. Identification of Arhgap28, a new regulator of stress fibre formation in cells assembling a fibrous extracellular matrix. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2019 Dec 14]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/identification-of-arhgap28-a-new-regulator-of-stress-fibre-formation-in-cells-assembling-a-fibrous-extracellular-matrix(93164a99-54f1-4719-9eef-b81d3f3bc20e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559313.

Council of Science Editors:

Yeung C. Identification of Arhgap28, a new regulator of stress fibre formation in cells assembling a fibrous extracellular matrix. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/identification-of-arhgap28-a-new-regulator-of-stress-fibre-formation-in-cells-assembling-a-fibrous-extracellular-matrix(93164a99-54f1-4719-9eef-b81d3f3bc20e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559313

21. Yang, Youfeng. The Role Of Map Kinase Cascade In Msp Signaling Response.

Degree: PhD, 2010, University of Alabama – Birmingham

The MSP domain is an evolutionarily conserved immunoglobulin-like structure of about 120 amino acids (Miller et al., 2001). A P56S missense mutation in the MSP… (more)

Subjects/Keywords: Caenorhabditis elegans – metabolism.<; br>; Helminth Proteins – physiology.<; br>; MAP Kinase Signaling System – physiology.<; br>; Mitogen-Activated Protein Kinases – metabolism.<; br>; Oocytes – physiology<; br>; Reactive Oxygen Species – metabolism<; br>; Signal Transduction – physiology

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APA (6th Edition):

Yang, Y. (2010). The Role Of Map Kinase Cascade In Msp Signaling Response. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1399

Chicago Manual of Style (16th Edition):

Yang, Youfeng. “The Role Of Map Kinase Cascade In Msp Signaling Response.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1399.

MLA Handbook (7th Edition):

Yang, Youfeng. “The Role Of Map Kinase Cascade In Msp Signaling Response.” 2010. Web. 14 Dec 2019.

Vancouver:

Yang Y. The Role Of Map Kinase Cascade In Msp Signaling Response. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1399.

Council of Science Editors:

Yang Y. The Role Of Map Kinase Cascade In Msp Signaling Response. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1399

22. Mayhew, David Lawrence. Translation Initiation Signaling Components Altered By Mechanical Load Dictate Skeletal Muscle Hypertrophy.

Degree: PhD, 2010, University of Alabama – Birmingham

The regulation of protein synthesis (i.e., mRNA translation) is an energetically costly and extensively regulated process, which is primarily regulated at the initiation step. Mechanical… (more)

Subjects/Keywords: Eukaryotic Initiation Factor-2B – metabolism.<; br>; Muscle Proteins – metabolism.<; br>; Muscle, Skeletal<; br>; Physical Exertion<; br>; Physical Stimulation<; br>; Protein Biosynthesis<; br>; Resistance Training – adverse effects.<; br>; Signal Transduction

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APA (6th Edition):

Mayhew, D. L. (2010). Translation Initiation Signaling Components Altered By Mechanical Load Dictate Skeletal Muscle Hypertrophy. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1427

Chicago Manual of Style (16th Edition):

Mayhew, David Lawrence. “Translation Initiation Signaling Components Altered By Mechanical Load Dictate Skeletal Muscle Hypertrophy.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1427.

MLA Handbook (7th Edition):

Mayhew, David Lawrence. “Translation Initiation Signaling Components Altered By Mechanical Load Dictate Skeletal Muscle Hypertrophy.” 2010. Web. 14 Dec 2019.

Vancouver:

Mayhew DL. Translation Initiation Signaling Components Altered By Mechanical Load Dictate Skeletal Muscle Hypertrophy. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1427.

Council of Science Editors:

Mayhew DL. Translation Initiation Signaling Components Altered By Mechanical Load Dictate Skeletal Muscle Hypertrophy. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1427

23. Anderson, Mark Edwin. Exploring Health Disparities For Children In The City Of Milwaukee.

Degree: PhD, 2012, University of Alabama – Birmingham

This study investigated whether school-based oral health programs as a public policy intervention increased dental sealant applications among children from low-income families and minorities in… (more)

Subjects/Keywords: CD8-Positive T-Lymphocytes – metabolism.<; br>; Cytokines<; br>; Epigenomics.<; br>; STAT4 Transcription Factor – metabolism.<; br>; T-Box Domain Proteins – metabolism.<; br>; T-Lymphocytes, Helper-Inducer<; br>; Th1 Cells – metabolism.<; br>; Transcription Factor RelA – metabolism.

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APA (6th Edition):

Anderson, M. E. (2012). Exploring Health Disparities For Children In The City Of Milwaukee. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1398

Chicago Manual of Style (16th Edition):

Anderson, Mark Edwin. “Exploring Health Disparities For Children In The City Of Milwaukee.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1398.

MLA Handbook (7th Edition):

Anderson, Mark Edwin. “Exploring Health Disparities For Children In The City Of Milwaukee.” 2012. Web. 14 Dec 2019.

Vancouver:

Anderson ME. Exploring Health Disparities For Children In The City Of Milwaukee. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1398.

Council of Science Editors:

Anderson ME. Exploring Health Disparities For Children In The City Of Milwaukee. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1398

24. Murakami, Miho. Fiber modification of adenoviral vectors for cancer gene therapy.

Degree: PhD, 2010, University of Alabama – Birmingham

Cancer still remains a major public health concern despite improvements in primary prevention, early detection and advanced treatments. Cancer gene therapy using human adenovirus serotype… (more)

Subjects/Keywords: Adenoviruses, Human<; br>; Capsid Proteins<; br>; Gene Therapy  – methods<; br>; Genetic Vectors<; br>; Prostatic Neoplasms  – genetics<; br>; Recombinant Fusion Proteins  – metabolism<; br>; Transduction, Genetic<; br>; Viral Tropism  – physiology

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APA (6th Edition):

Murakami, M. (2010). Fiber modification of adenoviral vectors for cancer gene therapy. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1166

Chicago Manual of Style (16th Edition):

Murakami, Miho. “Fiber modification of adenoviral vectors for cancer gene therapy.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1166.

MLA Handbook (7th Edition):

Murakami, Miho. “Fiber modification of adenoviral vectors for cancer gene therapy.” 2010. Web. 14 Dec 2019.

Vancouver:

Murakami M. Fiber modification of adenoviral vectors for cancer gene therapy. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1166.

Council of Science Editors:

Murakami M. Fiber modification of adenoviral vectors for cancer gene therapy. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1166

25. Buckoreelall, Kajal. Identification and characterization of novel adenosine cleavage enzymes in mycobacteria.

Degree: PhD, 2011, University of Alabama – Birmingham

Tuberculosis (TB) is one of the leading infectious diseases in the world. An estimated one third of the world’s population is infected with Mycobacterium tuberculosis,… (more)

Subjects/Keywords: Bacterial Proteins  – chemistry<; br>; Bacterial Proteins  – metabolism<; br>; Mycobacterium smegmatis  – enzymology<; br>; Mycobacterium tuberculosis  – enzymology<; br>; Purine-Nucleoside Phosphorylase  – chemistry<; br>; Purine-Nucleoside Phosphorylase  – metabolism

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APA (6th Edition):

Buckoreelall, K. (2011). Identification and characterization of novel adenosine cleavage enzymes in mycobacteria. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1136

Chicago Manual of Style (16th Edition):

Buckoreelall, Kajal. “Identification and characterization of novel adenosine cleavage enzymes in mycobacteria.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1136.

MLA Handbook (7th Edition):

Buckoreelall, Kajal. “Identification and characterization of novel adenosine cleavage enzymes in mycobacteria.” 2011. Web. 14 Dec 2019.

Vancouver:

Buckoreelall K. Identification and characterization of novel adenosine cleavage enzymes in mycobacteria. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1136.

Council of Science Editors:

Buckoreelall K. Identification and characterization of novel adenosine cleavage enzymes in mycobacteria. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1136

26. Kapoor, Niren. Role of epithelial sodium channel and acid sensing ion channel in glioblastoma multiforme.

Degree: PhD, 2010, University of Alabama – Birmingham

Glioblastoma Multifrome is the most common and aggressive of the primary brain tumors. These tumors express multiple members of the Epithelial Sodium Channel (ENaC)/Degenerin (Deg)… (more)

Subjects/Keywords: Cell Movement<; br>; Epithelial Sodium Channel  – metabolism<; br>; Glioblastoma  – mortality<; br>; Membrane Potentials<; br>; Nerve Tissue Proteins  – metabolism<; br>; Sodium Channels  – metabolism

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APA (6th Edition):

Kapoor, N. (2010). Role of epithelial sodium channel and acid sensing ion channel in glioblastoma multiforme. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,914

Chicago Manual of Style (16th Edition):

Kapoor, Niren. “Role of epithelial sodium channel and acid sensing ion channel in glioblastoma multiforme.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,914.

MLA Handbook (7th Edition):

Kapoor, Niren. “Role of epithelial sodium channel and acid sensing ion channel in glioblastoma multiforme.” 2010. Web. 14 Dec 2019.

Vancouver:

Kapoor N. Role of epithelial sodium channel and acid sensing ion channel in glioblastoma multiforme. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,914.

Council of Science Editors:

Kapoor N. Role of epithelial sodium channel and acid sensing ion channel in glioblastoma multiforme. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,914

27. King, Adrienne Lester. Chronic alcohol consumption promotes opening of the mitochondrial permeability transition pore and increases mitochondrial injury in liver.

Degree: PhD, 2010, University of Alabama – Birmingham

Alcoholic liver disease is a serious public health concern. In particular, the mitochondrion is a specific target of ethanol toxicity and much of the damage… (more)

Subjects/Keywords: Alcohols  – pharmacology<; br>; Calcium  – metabolism<; br>; Cyclophilins  – metabolism<; br>; Ethanol  – adverse effects<; br>; Fatty Liver  – chemically induced<; br>; Liver  – drug effects<; br>; Mitochondria  – pathology<; br>; Mitochondrial Membrane Transport Proteins  – metabolism<; br>; Oxidative Stress

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APA (6th Edition):

King, A. L. (2010). Chronic alcohol consumption promotes opening of the mitochondrial permeability transition pore and increases mitochondrial injury in liver. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,842

Chicago Manual of Style (16th Edition):

King, Adrienne Lester. “Chronic alcohol consumption promotes opening of the mitochondrial permeability transition pore and increases mitochondrial injury in liver.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,842.

MLA Handbook (7th Edition):

King, Adrienne Lester. “Chronic alcohol consumption promotes opening of the mitochondrial permeability transition pore and increases mitochondrial injury in liver.” 2010. Web. 14 Dec 2019.

Vancouver:

King AL. Chronic alcohol consumption promotes opening of the mitochondrial permeability transition pore and increases mitochondrial injury in liver. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,842.

Council of Science Editors:

King AL. Chronic alcohol consumption promotes opening of the mitochondrial permeability transition pore and increases mitochondrial injury in liver. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,842

28. Phipps, Matthew Christopher. Development Of Electrospun Bone-Mimetic Matrices For Bone Regenerative Applications.

Degree: PhD, 2012, University of Alabama – Birmingham

Although bone has a dramatic capacity for regeneration, certain injuries and procedures present defects that are unable to heal properly, requiring surgical intervention to induce… (more)

Subjects/Keywords: Apoptosis – drug effects<; br>; beta Catenin – metabolism.<; br>; Breast Neoplasms – drug therapy<; br>; Cell Proliferation – drug effects.<; br>; Cyclic GMP-Dependent Protein Kinases – metabolism.<; br>; Cyclic Nucleotide Phosphodiesterases, Type 5 – genetics.<; br>; Phosphodiesterase 5 Inhibitors.<; br>; Sulindac – analogs & derivatives.<; br>; Wnt Proteins – metabolism.

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

APA (6th Edition):

Phipps, M. C. (2012). Development Of Electrospun Bone-Mimetic Matrices For Bone Regenerative Applications. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1410

Chicago Manual of Style (16th Edition):

Phipps, Matthew Christopher. “Development Of Electrospun Bone-Mimetic Matrices For Bone Regenerative Applications.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1410.

MLA Handbook (7th Edition):

Phipps, Matthew Christopher. “Development Of Electrospun Bone-Mimetic Matrices For Bone Regenerative Applications.” 2012. Web. 14 Dec 2019.

Vancouver:

Phipps MC. Development Of Electrospun Bone-Mimetic Matrices For Bone Regenerative Applications. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1410.

Council of Science Editors:

Phipps MC. Development Of Electrospun Bone-Mimetic Matrices For Bone Regenerative Applications. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1410

29. Cook, Leah M. (Leah Marie). Understanding molecular mechanisms of breast cancer metastasis using genetically-engineered mice.

Degree: PhD, 2011, University of Alabama – Birmingham

Morbidity and mortality of breast cancer patients are drastically increased when primary tumor cells metastasize to distant organ sites. Effective treatment of metastatic disease has… (more)

Subjects/Keywords: Breast Neoplasms  – pathology<; br>; Mammary Neoplasms, Animal<; br>; Mice, Transgenic<; br>; Neoplasm Metastasis  – pathology<; br>; Tumor Microenvironment<; br>; Tumor Suppressor Proteins  – genetics<; br>; Tumor Suppressor Proteins  – metabolism

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

APA (6th Edition):

Cook, L. M. (. M. (2011). Understanding molecular mechanisms of breast cancer metastasis using genetically-engineered mice. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1045

Chicago Manual of Style (16th Edition):

Cook, Leah M (Leah Marie). “Understanding molecular mechanisms of breast cancer metastasis using genetically-engineered mice.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1045.

MLA Handbook (7th Edition):

Cook, Leah M (Leah Marie). “Understanding molecular mechanisms of breast cancer metastasis using genetically-engineered mice.” 2011. Web. 14 Dec 2019.

Vancouver:

Cook LM(M. Understanding molecular mechanisms of breast cancer metastasis using genetically-engineered mice. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1045.

Council of Science Editors:

Cook LM(M. Understanding molecular mechanisms of breast cancer metastasis using genetically-engineered mice. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1045

30. Ling, Shiyun. Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation.

Degree: PhD, 2010, University of Alabama – Birmingham

Unrestricted cell proliferation and suppression of cell death are two essential events for tumor development. My dissertation research involves two proteins, 14-3-3 &tau and EDD… (more)

Subjects/Keywords: 14-3-3 Proteins – metabolism.<; br>; Breast Neoplasms<; br>; Down-Regulation<; br>; Membrane Proteins – genetics<; br>; Ovarian Neoplasms<; br>; Protein Processing, Post-Translational<; br>; Transcriptional Activation

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

APA (6th Edition):

Ling, S. (2010). Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1419

Chicago Manual of Style (16th Edition):

Ling, Shiyun. “Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 14, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1419.

MLA Handbook (7th Edition):

Ling, Shiyun. “Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation.” 2010. Web. 14 Dec 2019.

Vancouver:

Ling S. Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 14]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1419.

Council of Science Editors:

Ling S. Role Of 14-3-3&tau In Autophagy And Role Of Edd In P53 Regulation. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1419

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