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You searched for subject:( Qa SNARE Proteins genetics 60). Showing records 1 – 30 of 34888 total matches.

[1] [2] [3] [4] [5] … [1163]

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1. Parish, Lindsay A. Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes.

Degree: PhD, 2009, University of Alabama – Birmingham

Malaria is a mosquito-borne infectious disease that is caused by parasites in the genus Plasmodium. There are four species of malaria that routinely infect humans,… (more)

Subjects/Keywords: Erythrocytes  – metabolism<; br>; Plasmodium falciparum  – metabolism<; br>; Protozoan Proteins  – genetics<; br>; Qa-SNARE Proteins  – genetics<; br>; Secretory Pathway  – genetics

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

APA (6th Edition):

Parish, L. A. (2009). Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,503

Chicago Manual of Style (16th Edition):

Parish, Lindsay A. “Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,503.

MLA Handbook (7th Edition):

Parish, Lindsay A. “Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes.” 2009. Web. 06 Dec 2019.

Vancouver:

Parish LA. Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,503.

Council of Science Editors:

Parish LA. Protein trafficking and 4.1R relocalization in Plasmodium falciparum-infected erythrocytes. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,503

2. Galloway, Summer E. Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing.

Degree: PhD, 2008, University of Alabama – Birmingham

Vesicular stomatitis virus (VSV) encodes an RNA-dependent RNA polymerase (RdRp) composed of the 240 kDa large (L) catalytic protein and the phosphoprotein, which replicate the… (more)

Subjects/Keywords: Archaeal Proteins  – chemistry<; br>; Archaeal Proteins  – genetics<; br>; Methyltransferases  – chemistry<; br>; Methyltransferases  – genetics<; br>; RNA Replicase  – chemistry<; br>; RNA Replicase  – genetics<; br>; Viral Proteins  – chemistry<; br>; Viral Proteins  – genetics

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APA (6th Edition):

Galloway, S. E. (2008). Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,668

Chicago Manual of Style (16th Edition):

Galloway, Summer E. “Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,668.

MLA Handbook (7th Edition):

Galloway, Summer E. “Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing.” 2008. Web. 06 Dec 2019.

Vancouver:

Galloway SE. Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,668.

Council of Science Editors:

Galloway SE. Functional characterization of conserved domains within the L protein component of the vesicular stomatitis virus RNA-dependent RNA polymerase: implications for transcription and MRNA processing. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,668


University of Texas Southwestern Medical Center

3. Xu, Yi. Structural and Functional Studies of Munc18 and SNARE Proteins.

Degree: 2011, University of Texas Southwestern Medical Center

 Release of neurotransmitters is a tightly regulated process and a key event in interneuron communication. Release involves a series of steps, including vesicles docking to… (more)

Subjects/Keywords: SNARE Proteins; Munc18 Proteins; Nerve Tissue Proteins

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APA (6th Edition):

Xu, Y. (2011). Structural and Functional Studies of Munc18 and SNARE Proteins. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/893

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):

Xu, Yi. “Structural and Functional Studies of Munc18 and SNARE Proteins.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed December 06, 2019. http://hdl.handle.net/2152.5/893.

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

MLA Handbook (7th Edition):

Xu, Yi. “Structural and Functional Studies of Munc18 and SNARE Proteins.” 2011. Web. 06 Dec 2019.

Vancouver:

Xu Y. Structural and Functional Studies of Munc18 and SNARE Proteins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2019 Dec 06]. Available from: http://hdl.handle.net/2152.5/893.

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

Council of Science Editors:

Xu Y. Structural and Functional Studies of Munc18 and SNARE Proteins. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/893

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


University of Texas Southwestern Medical Center

4. Craig, Timothy Kellogg. Structure and Function of Proteins Involved in Regulated Secretion: Synaptotagmins and Complexin.

Degree: 2010, University of Texas Southwestern Medical Center

 The release of neurotransmitter from neurons is a tightly regulated process. There are a number of proteins required for membrane fusion to occur, and then… (more)

Subjects/Keywords: Synaptotagmins; Neurotransmitter Agents; SNARE Proteins

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APA (6th Edition):

Craig, T. K. (2010). Structure and Function of Proteins Involved in Regulated Secretion: Synaptotagmins and Complexin. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/896

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):

Craig, Timothy Kellogg. “Structure and Function of Proteins Involved in Regulated Secretion: Synaptotagmins and Complexin.” 2010. Thesis, University of Texas Southwestern Medical Center. Accessed December 06, 2019. http://hdl.handle.net/2152.5/896.

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

MLA Handbook (7th Edition):

Craig, Timothy Kellogg. “Structure and Function of Proteins Involved in Regulated Secretion: Synaptotagmins and Complexin.” 2010. Web. 06 Dec 2019.

Vancouver:

Craig TK. Structure and Function of Proteins Involved in Regulated Secretion: Synaptotagmins and Complexin. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2010. [cited 2019 Dec 06]. Available from: http://hdl.handle.net/2152.5/896.

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

Council of Science Editors:

Craig TK. Structure and Function of Proteins Involved in Regulated Secretion: Synaptotagmins and Complexin. [Thesis]. University of Texas Southwestern Medical Center; 2010. Available from: http://hdl.handle.net/2152.5/896

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

5. Kaufman, Greer E. (Greer Elizabeth). Characterization of a global regulatory pathway in Streptococcus pneumoniae.

Degree: PhD, 2007, University of Alabama – Birmingham

Streptococcus pneumoniae is a versatile organism that adapts to many different environments in the host. S. pneumoniae can asymptomatically colonize the nasopharynx of humans. However,… (more)

Subjects/Keywords: Bacterial Proteins  – genetics <; br>; DNA-Binding Proteins  – genetics <; br>; Operon <; br>; Repressor Proteins  – genetics <; br>; Streptococcus pneumoniae  – genetics <; br>; beta-Galactosidase  – genetics

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

APA (6th Edition):

Kaufman, G. E. (. E. (2007). Characterization of a global regulatory pathway in Streptococcus pneumoniae. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,181

Chicago Manual of Style (16th Edition):

Kaufman, Greer E (Greer Elizabeth). “Characterization of a global regulatory pathway in Streptococcus pneumoniae.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,181.

MLA Handbook (7th Edition):

Kaufman, Greer E (Greer Elizabeth). “Characterization of a global regulatory pathway in Streptococcus pneumoniae.” 2007. Web. 06 Dec 2019.

Vancouver:

Kaufman GE(E. Characterization of a global regulatory pathway in Streptococcus pneumoniae. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,181.

Council of Science Editors:

Kaufman GE(E. Characterization of a global regulatory pathway in Streptococcus pneumoniae. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,181

6. Harouaka, Djamila. Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication.

Degree: PhD, 2010, University of Alabama – Birmingham

The template for transcription and RNA replication for vesicular stomatitis virus (VSV) and other negative-strand RNA viruses is a ribonucleoprotein (RNP) complex consisting of the… (more)

Subjects/Keywords: Nucleocapsid Proteins  – chemistry<; br>; Nucleocapsid Proteins  – genetics<; br>; Reverse Transcription  – genetics<; br>; RNA, Viral  – genetics<; br>; Vesiculovirus  – genetics<; br>; Vesiculovirus  – physiology<; br>; Virus Replication – genetics

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

APA (6th Edition):

Harouaka, D. (2010). Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,848

Chicago Manual of Style (16th Edition):

Harouaka, Djamila. “Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,848.

MLA Handbook (7th Edition):

Harouaka, Djamila. “Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication.” 2010. Web. 06 Dec 2019.

Vancouver:

Harouaka D. Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,848.

Council of Science Editors:

Harouaka D. Investigation of residues of the vesicular stomatitis virus nucleocapsid protein that affect transcription and RNA replication. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,848

7. Furgason, Melonnie Lynn Marie. VPS45p as a Model System for Elucidation of SEC1/MUNC18 Protein Function: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Department of Biochemistry and Molecular Pharmacology, 2008, U of Massachusetts : Med

  Vesicular trafficking, the movement of vesicles between organelles and the plasma membrane for secretion, consists of multiple highly regulated processes. Many protein families function… (more)

Subjects/Keywords: Vesicular Transport Proteins; Drosophila Proteins; Munc18 Proteins; SNARE Proteins; Qa-SNARE Proteins; Neurons; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research

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APA (6th Edition):

Furgason, M. L. M. (2008). VPS45p as a Model System for Elucidation of SEC1/MUNC18 Protein Function: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/425

Chicago Manual of Style (16th Edition):

Furgason, Melonnie Lynn Marie. “VPS45p as a Model System for Elucidation of SEC1/MUNC18 Protein Function: A Dissertation.” 2008. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 06, 2019. https://escholarship.umassmed.edu/gsbs_diss/425.

MLA Handbook (7th Edition):

Furgason, Melonnie Lynn Marie. “VPS45p as a Model System for Elucidation of SEC1/MUNC18 Protein Function: A Dissertation.” 2008. Web. 06 Dec 2019.

Vancouver:

Furgason MLM. VPS45p as a Model System for Elucidation of SEC1/MUNC18 Protein Function: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2008. [cited 2019 Dec 06]. Available from: https://escholarship.umassmed.edu/gsbs_diss/425.

Council of Science Editors:

Furgason MLM. VPS45p as a Model System for Elucidation of SEC1/MUNC18 Protein Function: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2008. Available from: https://escholarship.umassmed.edu/gsbs_diss/425

8. Odom, Mary Rebecca. Poxvirus evolution: the role of horizontal gene transfer.

Degree: PhD, 2010, University of Alabama – Birmingham

We have investigated the set of all poxvirus proteins for information about the origins of protein coding genes of the Poxviridae family of viruses. A… (more)

Subjects/Keywords: Computational Biology  – methods<; br>; Evolution, Molecular<; br>; Gene Transfer, Horizontal<; br>; Phylogeny<; br>; Poxviridae  – genetics<; br>; Viral Proteins  – genetics

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APA (6th Edition):

Odom, M. R. (2010). Poxvirus evolution: the role of horizontal gene transfer. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,653

Chicago Manual of Style (16th Edition):

Odom, Mary Rebecca. “Poxvirus evolution: the role of horizontal gene transfer.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,653.

MLA Handbook (7th Edition):

Odom, Mary Rebecca. “Poxvirus evolution: the role of horizontal gene transfer.” 2010. Web. 06 Dec 2019.

Vancouver:

Odom MR. Poxvirus evolution: the role of horizontal gene transfer. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,653.

Council of Science Editors:

Odom MR. Poxvirus evolution: the role of horizontal gene transfer. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,653

9. Smith, Rebecca Burt. Axonal trafficking of BMP signals in Drosophila motoneurons.

Degree: PhD, 2009, University of Alabama – Birmingham

The Drosophila Bone Morphogenetic Protein (BMP) Glass bottom boat (Gbb) is a ligand for the BMP type II receptor, Wishful thinking (Wit). Mutations in either… (more)

Subjects/Keywords: Axonal Transport<; br>; Bone Morphogenetic Proteins  – genetics<; br>; Drosophila  – genetics<; br>; Motor Neurons<; br>; Neuronal Plasticity<; br>; Synapses  – physiology

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APA (6th Edition):

Smith, R. B. (2009). Axonal trafficking of BMP signals in Drosophila motoneurons. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,930

Chicago Manual of Style (16th Edition):

Smith, Rebecca Burt. “Axonal trafficking of BMP signals in Drosophila motoneurons.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,930.

MLA Handbook (7th Edition):

Smith, Rebecca Burt. “Axonal trafficking of BMP signals in Drosophila motoneurons.” 2009. Web. 06 Dec 2019.

Vancouver:

Smith RB. Axonal trafficking of BMP signals in Drosophila motoneurons. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,930.

Council of Science Editors:

Smith RB. Axonal trafficking of BMP signals in Drosophila motoneurons. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,930

10. Li, Xingnan. Regulation of [beta]-catenin by Gli1 in epithelial transformation.

Degree: PhD, 2006, University of Alabama – Birmingham

Gli family members-mediated continuous Hedgehog (Hh) pathway activity plays a role in the growth of a number of human cancers, including the common malignancy of… (more)

Subjects/Keywords: beta Catenin  – metabolism <; br>; Cell Transformation, Neoplastic  – genetics <; br>; Oncogene Proteins <; br>; Trans-Activators  – genetics <; br>; Transcription, Genetic

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APA (6th Edition):

Li, X. (2006). Regulation of [beta]-catenin by Gli1 in epithelial transformation. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,90

Chicago Manual of Style (16th Edition):

Li, Xingnan. “Regulation of [beta]-catenin by Gli1 in epithelial transformation.” 2006. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,90.

MLA Handbook (7th Edition):

Li, Xingnan. “Regulation of [beta]-catenin by Gli1 in epithelial transformation.” 2006. Web. 06 Dec 2019.

Vancouver:

Li X. Regulation of [beta]-catenin by Gli1 in epithelial transformation. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2006. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,90.

Council of Science Editors:

Li X. Regulation of [beta]-catenin by Gli1 in epithelial transformation. [Doctoral Dissertation]. University of Alabama – Birmingham; 2006. Available from: http://contentdm.mhsl.uab.edu/u?/etd,90

11. Douglas, Chanel Catherine. A study into the protein/protein interactions involved in HIV-1 capsid assembly.

Degree: PhD, 2007, University of Alabama – Birmingham

The aim of this work was to build an understanding of the protein/protein interactions involved in HIV-1 capsid assembly as it relates to the condensation… (more)

Subjects/Keywords: Capsid Proteins  – chemistry <; br>; HIV-1  – chemistry <; br>; Mutation  – genetics <; br>; Protein Binding <; br>; Static Electricity <; br>; Virus Assembly

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APA (6th Edition):

Douglas, C. C. (2007). A study into the protein/protein interactions involved in HIV-1 capsid assembly. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,363

Chicago Manual of Style (16th Edition):

Douglas, Chanel Catherine. “A study into the protein/protein interactions involved in HIV-1 capsid assembly.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,363.

MLA Handbook (7th Edition):

Douglas, Chanel Catherine. “A study into the protein/protein interactions involved in HIV-1 capsid assembly.” 2007. Web. 06 Dec 2019.

Vancouver:

Douglas CC. A study into the protein/protein interactions involved in HIV-1 capsid assembly. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,363.

Council of Science Editors:

Douglas CC. A study into the protein/protein interactions involved in HIV-1 capsid assembly. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,363

12. Chang, Jenny Ren-Jye. Scaffolding-mediated capsid size determination in bacteriophages.

Degree: PhD, 2009, University of Alabama – Birmingham

Bacteriophage P2 encodes a scaffolding protein (gpO), which is required for correct assembly of P2 procapsids from the major capsid protein (gpN). The 284-residue gpO… (more)

Subjects/Keywords: Bacteriophages <; br>; DNA viruses <; br>; Scaffold proteins <; br>; Viruses  – Morphology <; br>; Viral genetics <; br>; Staphylococcus aureus.

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APA (6th Edition):

Chang, J. R. (2009). Scaffolding-mediated capsid size determination in bacteriophages. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,562

Chicago Manual of Style (16th Edition):

Chang, Jenny Ren-Jye. “Scaffolding-mediated capsid size determination in bacteriophages.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,562.

MLA Handbook (7th Edition):

Chang, Jenny Ren-Jye. “Scaffolding-mediated capsid size determination in bacteriophages.” 2009. Web. 06 Dec 2019.

Vancouver:

Chang JR. Scaffolding-mediated capsid size determination in bacteriophages. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,562.

Council of Science Editors:

Chang JR. Scaffolding-mediated capsid size determination in bacteriophages. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,562

13. Nelson, Michael Paul. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.

Degree: PhD, 2012, University of Alabama – Birmingham

Pneumonia caused by the fungal pathogen Pneumocystis continues to be the leading cause of morbidity and mortality in AIDS patients. In addition, there are a… (more)

Subjects/Keywords: CD8-Positive T-Lymphocytes – immunology.<; br>; Cell Differentiation – genetics<; br>; Evolution, Molecular.<; br>; Genome, Viral<; br>; HIV Infections<; br>; HIV-1 – immunology<; br>; Immune Evasion.<; br>; Mutation, Missense<; br>; Phenotype<; br>; T-Box Domain Proteins – genetics.<; br>; Viral Proteins – immunology.

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APA (6th Edition):

Nelson, M. P. (2012). Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1409

Chicago Manual of Style (16th Edition):

Nelson, Michael Paul. “Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1409.

MLA Handbook (7th Edition):

Nelson, Michael Paul. “Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina.” 2012. Web. 06 Dec 2019.

Vancouver:

Nelson MP. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1409.

Council of Science Editors:

Nelson MP. Innate Immune Mechanisms Against The Atypical Fungal Pathogen Pneumocystis Murina. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1409


University of Texas Southwestern Medical Center

14. Kaeser-Woo, Yea Jin. Regulation of SNARE-Mediated Synaptic Vesicle Release by Synaptotagmins and Complexins.

Degree: 2010, University of Texas Southwestern Medical Center

 In the brain, neurons communicate with each other by synaptic transmission. This process includes release of neurotransmitter from vesicles in the presynaptic neuron into the… (more)

Subjects/Keywords: Synaptic Transmission; Calcium Signaling; SNARE Proteins

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APA (6th Edition):

Kaeser-Woo, Y. J. (2010). Regulation of SNARE-Mediated Synaptic Vesicle Release by Synaptotagmins and Complexins. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/806

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):

Kaeser-Woo, Yea Jin. “Regulation of SNARE-Mediated Synaptic Vesicle Release by Synaptotagmins and Complexins.” 2010. Thesis, University of Texas Southwestern Medical Center. Accessed December 06, 2019. http://hdl.handle.net/2152.5/806.

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

MLA Handbook (7th Edition):

Kaeser-Woo, Yea Jin. “Regulation of SNARE-Mediated Synaptic Vesicle Release by Synaptotagmins and Complexins.” 2010. Web. 06 Dec 2019.

Vancouver:

Kaeser-Woo YJ. Regulation of SNARE-Mediated Synaptic Vesicle Release by Synaptotagmins and Complexins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2010. [cited 2019 Dec 06]. Available from: http://hdl.handle.net/2152.5/806.

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

Council of Science Editors:

Kaeser-Woo YJ. Regulation of SNARE-Mediated Synaptic Vesicle Release by Synaptotagmins and Complexins. [Thesis]. University of Texas Southwestern Medical Center; 2010. Available from: http://hdl.handle.net/2152.5/806

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


University of Texas Southwestern Medical Center

15. Brewer, Kyle Daniel. Studies on the Structure and Interactions of Synaptotagmin-1 and SNARE Proteins in Neurotransmitter Release.

Degree: 2014, University of Texas Southwestern Medical Center

 The SNARE complex and synaptotagmin-1 are essential for Ca²⁺-evoked neurotransmitter release, yet the mechanism of how these proteins work together in membrane fusion is unclear.… (more)

Subjects/Keywords: Membrane Fusion; SNARE Proteins; Synaptotagmin I

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APA (6th Edition):

Brewer, K. D. (2014). Studies on the Structure and Interactions of Synaptotagmin-1 and SNARE Proteins in Neurotransmitter Release. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3946

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):

Brewer, Kyle Daniel. “Studies on the Structure and Interactions of Synaptotagmin-1 and SNARE Proteins in Neurotransmitter Release.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed December 06, 2019. http://hdl.handle.net/2152.5/3946.

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

MLA Handbook (7th Edition):

Brewer, Kyle Daniel. “Studies on the Structure and Interactions of Synaptotagmin-1 and SNARE Proteins in Neurotransmitter Release.” 2014. Web. 06 Dec 2019.

Vancouver:

Brewer KD. Studies on the Structure and Interactions of Synaptotagmin-1 and SNARE Proteins in Neurotransmitter Release. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 Dec 06]. Available from: http://hdl.handle.net/2152.5/3946.

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

Council of Science Editors:

Brewer KD. Studies on the Structure and Interactions of Synaptotagmin-1 and SNARE Proteins in Neurotransmitter Release. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3946

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

16. 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 06, 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. 06 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 06]. 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

17. 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 06, 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. 06 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 06]. 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

18. Dearborn, Altaira D. Scaffold-mediated size determination of bacteriophage capsids by mobile genetic elements.

Degree: PhD, 2012, University of Alabama – Birmingham

Bacteriophage can mediate the transfer of unrelated mobile genetic elements (MGE) from a carrier bacterial cell to the susceptible population around it. This transfer results… (more)

Subjects/Keywords: Capsid  – physiology<; br>; Capsid Proteins  – physiology<; br>; Genomic Islands  – genetics<; br>; Organelle Size  – genetics<; br>; Staphylococcus aureus  – genetics<; br>; Virus Assembly  – genetics

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APA (6th Edition):

Dearborn, A. D. (2012). Scaffold-mediated size determination of bacteriophage capsids by mobile genetic elements. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1131

Chicago Manual of Style (16th Edition):

Dearborn, Altaira D. “Scaffold-mediated size determination of bacteriophage capsids by mobile genetic elements.” 2012. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1131.

MLA Handbook (7th Edition):

Dearborn, Altaira D. “Scaffold-mediated size determination of bacteriophage capsids by mobile genetic elements.” 2012. Web. 06 Dec 2019.

Vancouver:

Dearborn AD. Scaffold-mediated size determination of bacteriophage capsids by mobile genetic elements. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2012. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1131.

Council of Science Editors:

Dearborn AD. Scaffold-mediated size determination of bacteriophage capsids by mobile genetic elements. [Doctoral Dissertation]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1131

19. 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 06, 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. 06 Dec 2019.

Vancouver:

Dong S. Characterization of the oligosaccharides of B. anthracis exosporium. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Dec 06]. 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

20. Hock, Thomas D. Regulation of the human heme oxygenase-1 gene.

Degree: PhD, 2007, University of Alabama – Birmingham

The heme oxygenase-1 (HO-1) gene encodes a microsomal enzyme that catalyzes the conversion of heme to carbon monoxide, Iron, and biliverdin. HO-1 transcription is induced… (more)

Subjects/Keywords: Heme Oxygenase-1  – genetics <; br>; Proto-Oncogene Proteins c-jun  – metabolism <; br>; Transcription Factors  – metabolism

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APA (6th Edition):

Hock, T. D. (2007). Regulation of the human heme oxygenase-1 gene. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,126

Chicago Manual of Style (16th Edition):

Hock, Thomas D. “Regulation of the human heme oxygenase-1 gene.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,126.

MLA Handbook (7th Edition):

Hock, Thomas D. “Regulation of the human heme oxygenase-1 gene.” 2007. Web. 06 Dec 2019.

Vancouver:

Hock TD. Regulation of the human heme oxygenase-1 gene. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,126.

Council of Science Editors:

Hock TD. Regulation of the human heme oxygenase-1 gene. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,126

21. 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 (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 06, 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. 06 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 06]. 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

22. 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 (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 06, 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. 06 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 06]. 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

23. Thal, Melissa Ann. Characterization of the induction and regulation of early B cell development.

Degree: PhD, 2009, University of Alabama – Birmingham

Hematopoiesis is a highly regulated process directed by the microenvironment or niche in the bone marrow and the transcription factors those signals activate. Gene knockout… (more)

Subjects/Keywords: B-Lymphocytes  – cytology<; br>; Down-Regulation<; br>; Inhibitor of Differentiation Protein 2  – genetics<; br>; Inhibitor of Differentiation Proteins  – genetics<; br>; Receptors, Interleukin-7  – deficiency<; br>; TCF Transcription Factors  – physiology<; br>; Trans-Activators  – physiology

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APA (6th Edition):

Thal, M. A. (2009). Characterization of the induction and regulation of early B cell development. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,578

Chicago Manual of Style (16th Edition):

Thal, Melissa Ann. “Characterization of the induction and regulation of early B cell development.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,578.

MLA Handbook (7th Edition):

Thal, Melissa Ann. “Characterization of the induction and regulation of early B cell development.” 2009. Web. 06 Dec 2019.

Vancouver:

Thal MA. Characterization of the induction and regulation of early B cell development. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,578.

Council of Science Editors:

Thal MA. Characterization of the induction and regulation of early B cell development. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,578

24. Jordan, Stephen J. (Stephen James). Analysis of the malaria vaccine potential of Plasmodium falciparum merozoite surface protein-3.

Degree: PhD, 2009, University of Alabama – Birmingham

Malaria causes an estimated 1-3 million deaths each year, with the majority of deaths being a result of infection with Plasmodium falciparum. No commercially available… (more)

Subjects/Keywords: Antigens, Protozoan  – genetics<; br>; Antigens, Protozoan  – immunology<; br>; Genetic Variation<; br>; Malaria Vaccines  – immunology<; br>; Malaria, Falciparum  – prevention & control<; br>; Plasmodium falciparum  – immunology<; br>; Protozoan Proteins  – genetics

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APA (6th Edition):

Jordan, S. J. (. J. (2009). Analysis of the malaria vaccine potential of Plasmodium falciparum merozoite surface protein-3. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,674

Chicago Manual of Style (16th Edition):

Jordan, Stephen J (Stephen James). “Analysis of the malaria vaccine potential of Plasmodium falciparum merozoite surface protein-3.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,674.

MLA Handbook (7th Edition):

Jordan, Stephen J (Stephen James). “Analysis of the malaria vaccine potential of Plasmodium falciparum merozoite surface protein-3.” 2009. Web. 06 Dec 2019.

Vancouver:

Jordan SJ(J. Analysis of the malaria vaccine potential of Plasmodium falciparum merozoite surface protein-3. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,674.

Council of Science Editors:

Jordan SJ(J. Analysis of the malaria vaccine potential of Plasmodium falciparum merozoite surface protein-3. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,674

25. Spilman, Michael Scott. Molecular piracy in the mobilization of Staphylococcus aureus pathogenicity island 1.

Degree: PhD, 2011, University of Alabama – Birmingham

Staphylococcus aureus bacteriophage 80α is a temperate, double-stranded DNA phage that serves as a “helper” phage for the mobilization of several S. aureus pathogenicity islands… (more)

Subjects/Keywords: Bacteriophages  – ultrastructure<; br>; Capsid  – ultrastructure<; br>; Capsid Proteins  – ultrastructure<; br>; Genomic Islands  – genetics<; br>; Models, Molecular<; br>; Organelle Size  – genetics<; br>; Staphylococcus aureus  – virology

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APA (6th Edition):

Spilman, M. S. (2011). Molecular piracy in the mobilization of Staphylococcus aureus pathogenicity island 1. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1060

Chicago Manual of Style (16th Edition):

Spilman, Michael Scott. “Molecular piracy in the mobilization of Staphylococcus aureus pathogenicity island 1.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1060.

MLA Handbook (7th Edition):

Spilman, Michael Scott. “Molecular piracy in the mobilization of Staphylococcus aureus pathogenicity island 1.” 2011. Web. 06 Dec 2019.

Vancouver:

Spilman MS. Molecular piracy in the mobilization of Staphylococcus aureus pathogenicity island 1. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1060.

Council of Science Editors:

Spilman MS. Molecular piracy in the mobilization of Staphylococcus aureus pathogenicity island 1. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1060

26. Hollingsworth, T.j. The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation.

Degree: 2013, University of Alabama – Birmingham

Retinitis pigmentosa is one of the most common inherited blinding disorders, affecting 1 in 4000 individuals world-wide. Approximately 30% of retinitis pigmentosa cases are dominantly… (more)

Subjects/Keywords: Genes, Dominant – genetics.<; br>; Mutant Proteins – metabolism.<; br>; Mutation – genetics<; br>; Retinal Degeneration – metabolism.<; br>; Retinal Rod Photoreceptor Cells<; br>; Retinitis Pigmentosa<; br>; Rhodopsin – metabolism.

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APA (6th Edition):

Hollingsworth, T. j. (2013). The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1785

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):

Hollingsworth, T j. “The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation.” 2013. Thesis, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1785.

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

MLA Handbook (7th Edition):

Hollingsworth, T j. “The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation.” 2013. Web. 06 Dec 2019.

Vancouver:

Hollingsworth Tj. The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation. [Internet] [Thesis]. University of Alabama – Birmingham; 2013. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1785.

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

Council of Science Editors:

Hollingsworth Tj. The Role Of Autosomal Dominant Retinitis Pigmentosa Rhodopsin Mutant Ter349glu In Rod Cell Biogenesis And Retinal Inflammation. [Thesis]. University of Alabama – Birmingham; 2013. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1785

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

27. Tang, Yizhe. Modification of adenovirus capsid proteins for gene therapy applications.

Degree: PhD, 2009, University of Alabama – Birmingham

Adenovirus (Ad) is the most commonly used viral vector in gene therapy applications to date for a broad range of diseases. Although Ad-based viral vectors… (more)

Subjects/Keywords: Adenoviridae  – genetics<; br>; Adenoviridae Infections  – metabolism<; br>; Adenoviruses, Human  – genetics<; br>; Blood-Brain Barrier  – virology<; br>; Capsid Proteins  – chemistry<; br>; Gene Products, tat<; br>; Gene Therapy  – methods<; br>; Genetic Engineering<; br>; Neoplasms<; br>; Transduction, Genetic  – methods

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APA (6th Edition):

Tang, Y. (2009). Modification of adenovirus capsid proteins for gene therapy applications. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,675

Chicago Manual of Style (16th Edition):

Tang, Yizhe. “Modification of adenovirus capsid proteins for gene therapy applications.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,675.

MLA Handbook (7th Edition):

Tang, Yizhe. “Modification of adenovirus capsid proteins for gene therapy applications.” 2009. Web. 06 Dec 2019.

Vancouver:

Tang Y. Modification of adenovirus capsid proteins for gene therapy applications. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,675.

Council of Science Editors:

Tang Y. Modification of adenovirus capsid proteins for gene therapy applications. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,675

28. Mao,Weiming. The role of bHLH gene ash1 in the developing chick eye.

Degree: PhD, 2008, University of Alabama – Birmingham

Development of the vertebrate eye is controlled by a network of regulatory genes including those in the basic loop-helix-loop (bHLH) family. In this study, we… (more)

Subjects/Keywords: Amacrine Cells  – physiology<; br>; Avian Proteins  – metabolism<; br>; Basic Helix-Loop-Helix Transcription Factors  – metabolism<; br>; Gene Expression Regulation, Developmental  – physiology<; br>; Nerve Tissue Proteins  – genetics<; br>; Nuclear Reprogramming<; br>; Retina  – cytology<; br>; Retinal Neurons  – cytology Retinal Pigment Epithelium  – cytology<; br>; Stem Cells  – cytology

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APA (6th Edition):

Mao,Weiming. (2008). The role of bHLH gene ash1 in the developing chick eye. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,527

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Mao,Weiming. “The role of bHLH gene ash1 in the developing chick eye.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,527.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Mao,Weiming. “The role of bHLH gene ash1 in the developing chick eye.” 2008. Web. 06 Dec 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Mao,Weiming. The role of bHLH gene ash1 in the developing chick eye. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,527.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Mao,Weiming. The role of bHLH gene ash1 in the developing chick eye. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,527

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

29. Grunda, Jessica M. Identification of new strategies for the treatment of glioblastoma multiforme utilizing a pharmacogenomic approach: genetic profiles associated with patient prognosis and outcome to capecitabine treatment.

Degree: PhD, 2009, University of Alabama – Birmingham

Glioblastoma multiforme (GBM) is the most lethal form of primary brain neoplasm with average patient survival between 9 and 15 months even with the most… (more)

Subjects/Keywords: Brain Neoplasms<; br>; Drug Resistance, Neoplasm  – genetics<; br>; Endopeptidases  – metabolism<; br>; Gene Expression Profiling<; br>; Glioblastoma<; br>; Microtubule-Associated Proteins  – metabolism<; br>; Neoplasm Proteins  – metabolism<; br>; Thymidylate Synthase  – metabolism<; br>; Tumor Markers, Biological  – metabolism

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APA (6th Edition):

Grunda, J. M. (2009). Identification of new strategies for the treatment of glioblastoma multiforme utilizing a pharmacogenomic approach: genetic profiles associated with patient prognosis and outcome to capecitabine treatment. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1085

Chicago Manual of Style (16th Edition):

Grunda, Jessica M. “Identification of new strategies for the treatment of glioblastoma multiforme utilizing a pharmacogenomic approach: genetic profiles associated with patient prognosis and outcome to capecitabine treatment.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1085.

MLA Handbook (7th Edition):

Grunda, Jessica M. “Identification of new strategies for the treatment of glioblastoma multiforme utilizing a pharmacogenomic approach: genetic profiles associated with patient prognosis and outcome to capecitabine treatment.” 2009. Web. 06 Dec 2019.

Vancouver:

Grunda JM. Identification of new strategies for the treatment of glioblastoma multiforme utilizing a pharmacogenomic approach: genetic profiles associated with patient prognosis and outcome to capecitabine treatment. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1085.

Council of Science Editors:

Grunda JM. Identification of new strategies for the treatment of glioblastoma multiforme utilizing a pharmacogenomic approach: genetic profiles associated with patient prognosis and outcome to capecitabine treatment. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1085

30. Kallmeyer, Adam K. (Adam Keith). Regulatory mechanisms of eukaryotic translation termination.

Degree: PhD, 2007, University of Alabama – Birmingham

Translation is separated into three distinct steps: initiation, elongation, and termination. Termination is mediated by a heterodimer of eRF1 and eRF3. eRF1 (encoded by the… (more)

Subjects/Keywords: Casein Kinase II  – metabolism<; br>; Peptide Termination Factors  – metabolism<; br>; Protein Biosynthesis  – physiology<; br>; Recombinant Fusion Proteins<; br>; Saccharomyces cerevisiae  – genetics<; br>; Saccharomyces cerevisiae Proteins  – metabolism

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

APA (6th Edition):

Kallmeyer, A. K. (. K. (2007). Regulatory mechanisms of eukaryotic translation termination. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,450

Chicago Manual of Style (16th Edition):

Kallmeyer, Adam K (Adam Keith). “Regulatory mechanisms of eukaryotic translation termination.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed December 06, 2019. http://contentdm.mhsl.uab.edu/u?/etd,450.

MLA Handbook (7th Edition):

Kallmeyer, Adam K (Adam Keith). “Regulatory mechanisms of eukaryotic translation termination.” 2007. Web. 06 Dec 2019.

Vancouver:

Kallmeyer AK(K. Regulatory mechanisms of eukaryotic translation termination. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Dec 06]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,450.

Council of Science Editors:

Kallmeyer AK(K. Regulatory mechanisms of eukaryotic translation termination. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,450

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