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You searched for subject:( Promoter Regions Genetic genetics 60). Showing records 1 – 30 of 36703 total matches.

[1] [2] [3] [4] [5] … [1224]

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1. Warram, Jason M. (Jason Morgan). Strategies for combined screening and imaging of breast cancer.

Degree: PhD, 2011, University of Alabama – Birmingham

Successful treatment of breast cancer directly correlates with tumor stage and grade at diagnosis. Early diagnosis leads to a five-year relative survival rate of 96.8%… (more)

Subjects/Keywords: Adenoviridae  – genetics<; br>; Breast Neoplasms  – diagnosis<; br>; Gene Therapy<; br>; Mass Screening  – methods<; br>; Microbubbles<; br>; Neoplasm Metastasis<; br>; Promoter Regions, Genetic  – genetics<; br>; Vascular Endothelial Growth Factor Receptor-2  – immunology

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

APA (6th Edition):

Warram, J. M. (. M. (2011). Strategies for combined screening and imaging of breast cancer. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,881

Chicago Manual of Style (16th Edition):

Warram, Jason M (Jason Morgan). “Strategies for combined screening and imaging of breast cancer.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,881.

MLA Handbook (7th Edition):

Warram, Jason M (Jason Morgan). “Strategies for combined screening and imaging of breast cancer.” 2011. Web. 29 Mar 2020.

Vancouver:

Warram JM(M. Strategies for combined screening and imaging of breast cancer. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,881.

Council of Science Editors:

Warram JM(M. Strategies for combined screening and imaging of breast cancer. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,881


University of Western Ontario

2. Rabbani, Mahnaz. Evolution of Mobile Promoters in Prokaryotic Genomes.

Degree: 2015, University of Western Ontario

 Mobile genetic elements are important factors in evolution, and greatly influence the structure of genomes, facilitating the development of new adaptive characteristics. The dynamics of… (more)

Subjects/Keywords: mobile genetic elements; mobile promoters; promoter regions; Applied Mathematics; Bioinformatics; Computational Biology; Genomics

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APA (6th Edition):

Rabbani, M. (2015). Evolution of Mobile Promoters in Prokaryotic Genomes. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3338

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):

Rabbani, Mahnaz. “Evolution of Mobile Promoters in Prokaryotic Genomes.” 2015. Thesis, University of Western Ontario. Accessed March 29, 2020. https://ir.lib.uwo.ca/etd/3338.

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

MLA Handbook (7th Edition):

Rabbani, Mahnaz. “Evolution of Mobile Promoters in Prokaryotic Genomes.” 2015. Web. 29 Mar 2020.

Vancouver:

Rabbani M. Evolution of Mobile Promoters in Prokaryotic Genomes. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2020 Mar 29]. Available from: https://ir.lib.uwo.ca/etd/3338.

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

Council of Science Editors:

Rabbani M. Evolution of Mobile Promoters in Prokaryotic Genomes. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/3338

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

3. Yeo, Sujeong. Transcriptional Regulation Of Gfap.

Degree: 2012, University of Alabama – Birmingham

Glial fibrillary acidic protein (GFAP) is an astrocytic intermediate filament protein whose levels are increased in response to CNS injuries. Aim one of my thesis… (more)

Subjects/Keywords: Astrocytes – metabolism<; /br>; Brain Injuries – metabolism.<; /br>; Epigenesis, Genetic.<; /br>; Gene Expression Regulation – physiology<; /br>; Glial Fibrillary Acidic Protein – genetics.<; /br>; Mice, Transgenic<; /br>; Promoter Regions, Genetic – physiology<; /br>; Transcription Factors – metabolism

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APA (6th Edition):

Yeo, S. (2012). Transcriptional Regulation Of Gfap. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1661

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):

Yeo, Sujeong. “Transcriptional Regulation Of Gfap.” 2012. Thesis, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1661.

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

MLA Handbook (7th Edition):

Yeo, Sujeong. “Transcriptional Regulation Of Gfap.” 2012. Web. 29 Mar 2020.

Vancouver:

Yeo S. Transcriptional Regulation Of Gfap. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1661.

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

Council of Science Editors:

Yeo S. Transcriptional Regulation Of Gfap. [Thesis]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1661

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


University of Cape Town

4. Wells, Carol Dawn. The functional significance of the G to A point mutation in the promoter region of the Apolipoprotein AI gene.

Degree: Image, Division of Medical Biochemistry & Structural Biology, 1993, University of Cape Town

 AG to A transition at position -76 in the promoter region of the apoAI gene was previously identified, and the A-76 has been shown to… (more)

Subjects/Keywords: Apolipoproteins - genetics; DNA-Binding Proteins - analysis; Genetic engineering; Point Mutation; Promoter Regions (Genetics); Protein engineering

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APA (6th Edition):

Wells, C. D. (1993). The functional significance of the G to A point mutation in the promoter region of the Apolipoprotein AI gene. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/27143

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):

Wells, Carol Dawn. “The functional significance of the G to A point mutation in the promoter region of the Apolipoprotein AI gene.” 1993. Thesis, University of Cape Town. Accessed March 29, 2020. http://hdl.handle.net/11427/27143.

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

MLA Handbook (7th Edition):

Wells, Carol Dawn. “The functional significance of the G to A point mutation in the promoter region of the Apolipoprotein AI gene.” 1993. Web. 29 Mar 2020.

Vancouver:

Wells CD. The functional significance of the G to A point mutation in the promoter region of the Apolipoprotein AI gene. [Internet] [Thesis]. University of Cape Town; 1993. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/11427/27143.

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

Council of Science Editors:

Wells CD. The functional significance of the G to A point mutation in the promoter region of the Apolipoprotein AI gene. [Thesis]. University of Cape Town; 1993. Available from: http://hdl.handle.net/11427/27143

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

5. McNamara, Ryan Philip. Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes.

Degree: 2015, University of Texas Southwestern Medical Center

 Gene expression of the human immunodeficiency virus (HIV) and cellular primary responsive genes (PRG’s) is regulated at the step of transcription elongation. Shortly after transcription… (more)

Subjects/Keywords: Phosphoprotein Phosphatases; Positive Transcriptional Elongation Factor B; Promoter Regions, Genetic; Ribonucleoproteins, Small Nuclear; Transcription Elongation, Genetic

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APA (6th Edition):

McNamara, R. P. (2015). Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2724

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):

McNamara, Ryan Philip. “Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed March 29, 2020. http://hdl.handle.net/2152.5/2724.

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

MLA Handbook (7th Edition):

McNamara, Ryan Philip. “Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes.” 2015. Web. 29 Mar 2020.

Vancouver:

McNamara RP. Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/2152.5/2724.

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

Council of Science Editors:

McNamara RP. Enzymatic Disassembly of Promoter Bound 7SK snRNP Drives Transcription Elongation of HIV and Cellular Genes. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/2724

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


University of Florida

6. Bruce, Wesley Bernard, 1959-. Characterization of functional domains of a T-DNA promoter active in sunflower tumors.

Degree: 1987, University of Florida

Subjects/Keywords: Boxes; DNA; Genes; Genetic mutation; Plasmids; Promoter regions; RNA; Sunflowers; TATA box; Tumors; Promoters (Genetics); Sunflowers  – Cytology; Tumors, Plant

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APA (6th Edition):

Bruce, Wesley Bernard, 1. (1987). Characterization of functional domains of a T-DNA promoter active in sunflower tumors. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00003369

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):

Bruce, Wesley Bernard, 1959-. “Characterization of functional domains of a T-DNA promoter active in sunflower tumors.” 1987. Thesis, University of Florida. Accessed March 29, 2020. http://ufdc.ufl.edu/AA00003369.

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

MLA Handbook (7th Edition):

Bruce, Wesley Bernard, 1959-. “Characterization of functional domains of a T-DNA promoter active in sunflower tumors.” 1987. Web. 29 Mar 2020.

Vancouver:

Bruce, Wesley Bernard 1. Characterization of functional domains of a T-DNA promoter active in sunflower tumors. [Internet] [Thesis]. University of Florida; 1987. [cited 2020 Mar 29]. Available from: http://ufdc.ufl.edu/AA00003369.

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

Council of Science Editors:

Bruce, Wesley Bernard 1. Characterization of functional domains of a T-DNA promoter active in sunflower tumors. [Thesis]. University of Florida; 1987. Available from: http://ufdc.ufl.edu/AA00003369

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

7. Heath, Cara Hope. Determinants that confer stop codon specificity to Tetrahymena thermophila eRF1.

Degree: MS, 2007, University of Alabama – Birmingham

In eukaryotes, translation termination is a process which is initiated by the presence of a stop codon in the A site of the ribosome and… (more)

Subjects/Keywords: Tetrahymena  – Genetics <; br>; Saccharomyces cerevisiae  – Genetics <; br>; Genetic translation.

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APA (6th Edition):

Heath, C. H. (2007). Determinants that confer stop codon specificity to Tetrahymena thermophila eRF1. (Masters Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,77

Chicago Manual of Style (16th Edition):

Heath, Cara Hope. “Determinants that confer stop codon specificity to Tetrahymena thermophila eRF1.” 2007. Masters Thesis, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,77.

MLA Handbook (7th Edition):

Heath, Cara Hope. “Determinants that confer stop codon specificity to Tetrahymena thermophila eRF1.” 2007. Web. 29 Mar 2020.

Vancouver:

Heath CH. Determinants that confer stop codon specificity to Tetrahymena thermophila eRF1. [Internet] [Masters thesis]. University of Alabama – Birmingham; 2007. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,77.

Council of Science Editors:

Heath CH. Determinants that confer stop codon specificity to Tetrahymena thermophila eRF1. [Masters Thesis]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,77

8. João Ramalho Ortigão-Farias. Caracterização de gene de quitinase de Lutzomyia longipalpis: descrição de processamento alternativo e busca por seqüência promotora.

Degree: 2009, Fundação Oswaldo Cruz

As leishmanioses são doenças causadas por protozoários do gênero Leishmania transmitidos pela picada de flebotomíneos infectados. Os atuais métodos de combate a estas moléstias têm… (more)

Subjects/Keywords: BIOLOGIA MOLECULAR; Processamento Alternativo; Regiões Promotoras Genéticas; Quitinase; Psychodidae; Chitinase; Genetic Promoter Regions; Psychodidae; Alternative Splicing

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APA (6th Edition):

Ortigão-Farias, J. R. (2009). Caracterização de gene de quitinase de Lutzomyia longipalpis: descrição de processamento alternativo e busca por seqüência promotora. (Thesis). Fundação Oswaldo Cruz. Retrieved from http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=253

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):

Ortigão-Farias, João Ramalho. “Caracterização de gene de quitinase de Lutzomyia longipalpis: descrição de processamento alternativo e busca por seqüência promotora.” 2009. Thesis, Fundação Oswaldo Cruz. Accessed March 29, 2020. http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=253.

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

MLA Handbook (7th Edition):

Ortigão-Farias, João Ramalho. “Caracterização de gene de quitinase de Lutzomyia longipalpis: descrição de processamento alternativo e busca por seqüência promotora.” 2009. Web. 29 Mar 2020.

Vancouver:

Ortigão-Farias JR. Caracterização de gene de quitinase de Lutzomyia longipalpis: descrição de processamento alternativo e busca por seqüência promotora. [Internet] [Thesis]. Fundação Oswaldo Cruz; 2009. [cited 2020 Mar 29]. Available from: http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=253.

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

Council of Science Editors:

Ortigão-Farias JR. Caracterização de gene de quitinase de Lutzomyia longipalpis: descrição de processamento alternativo e busca por seqüência promotora. [Thesis]. Fundação Oswaldo Cruz; 2009. Available from: http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=253

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


Lincoln University

9. Rasmussen, Katianna Louisa. Investigation of variation in the promoter region of the myostatin gene (GDF-8) in New Zealand cattle.

Degree: 2016, Lincoln University

 Myostatin, also called growth and differentiation factor 8 (GDF-8), has the specific function of negatively regulating muscle growth and muscle homeostasis through its interactions with… (more)

Subjects/Keywords: bovine; double-muscling; myostatin gene (MSTN); Promoter Regions, Genetic; GDF8; PCR- single strand conformational polymorphism (PCR-SSCP); cattle

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APA (6th Edition):

Rasmussen, K. L. (2016). Investigation of variation in the promoter region of the myostatin gene (GDF-8) in New Zealand cattle. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/7308

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):

Rasmussen, Katianna Louisa. “Investigation of variation in the promoter region of the myostatin gene (GDF-8) in New Zealand cattle.” 2016. Thesis, Lincoln University. Accessed March 29, 2020. http://hdl.handle.net/10182/7308.

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

MLA Handbook (7th Edition):

Rasmussen, Katianna Louisa. “Investigation of variation in the promoter region of the myostatin gene (GDF-8) in New Zealand cattle.” 2016. Web. 29 Mar 2020.

Vancouver:

Rasmussen KL. Investigation of variation in the promoter region of the myostatin gene (GDF-8) in New Zealand cattle. [Internet] [Thesis]. Lincoln University; 2016. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/10182/7308.

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

Council of Science Editors:

Rasmussen KL. Investigation of variation in the promoter region of the myostatin gene (GDF-8) in New Zealand cattle. [Thesis]. Lincoln University; 2016. Available from: http://hdl.handle.net/10182/7308

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


University of Florida

10. Barrow, Joeva Jade. Analyzing Beta-Globin Cis-Regulatory Elements By Using Artificial DNA-Binding Domains.

Degree: PhD, Medical Sciences - Biochemistry and Molecular Biology (IDP), 2013, University of Florida

 One of the primary methods to regulate gene expression is through the interaction of trans-factors with cis-regulatory DNA elements. Transcription factors bind in a DNA… (more)

Subjects/Keywords: Boxes; Cells; Chromatin; DNA; Gene therapy; Genetic loci; Hemoglobins; Promoter regions; RNA; Zinc; artificial  – beta-globin  – finger  – zinc

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APA (6th Edition):

Barrow, J. J. (2013). Analyzing Beta-Globin Cis-Regulatory Elements By Using Artificial DNA-Binding Domains. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045246

Chicago Manual of Style (16th Edition):

Barrow, Joeva Jade. “Analyzing Beta-Globin Cis-Regulatory Elements By Using Artificial DNA-Binding Domains.” 2013. Doctoral Dissertation, University of Florida. Accessed March 29, 2020. http://ufdc.ufl.edu/UFE0045246.

MLA Handbook (7th Edition):

Barrow, Joeva Jade. “Analyzing Beta-Globin Cis-Regulatory Elements By Using Artificial DNA-Binding Domains.” 2013. Web. 29 Mar 2020.

Vancouver:

Barrow JJ. Analyzing Beta-Globin Cis-Regulatory Elements By Using Artificial DNA-Binding Domains. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2020 Mar 29]. Available from: http://ufdc.ufl.edu/UFE0045246.

Council of Science Editors:

Barrow JJ. Analyzing Beta-Globin Cis-Regulatory Elements By Using Artificial DNA-Binding Domains. [Doctoral Dissertation]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045246


University of Florida

11. Brown, Sara. Functional genomics of LVIS_0853.

Degree: 2010, University of Florida

 LVIS_0853 is a member of the MarR family which has been historically linked to antibiotic resistance. Proteins from this family are able to bind a… (more)

Subjects/Keywords: Binding sites; Chemicals; DNA; Genomics; Ligands; Molecules; Operon; Promoter regions; Proteins; Sulfates; Genetic transcription – Regulation; Genomics

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

APA (6th Edition):

Brown, S. (2010). Functional genomics of LVIS_0853. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00060329

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):

Brown, Sara. “Functional genomics of LVIS_0853.” 2010. Thesis, University of Florida. Accessed March 29, 2020. http://ufdc.ufl.edu/AA00060329.

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

MLA Handbook (7th Edition):

Brown, Sara. “Functional genomics of LVIS_0853.” 2010. Web. 29 Mar 2020.

Vancouver:

Brown S. Functional genomics of LVIS_0853. [Internet] [Thesis]. University of Florida; 2010. [cited 2020 Mar 29]. Available from: http://ufdc.ufl.edu/AA00060329.

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

Council of Science Editors:

Brown S. Functional genomics of LVIS_0853. [Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/AA00060329

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


University of Florida

12. Warren, Soni A. Cardiac MLCK (cMLCK) and Its Role in Cardiac Function.

Degree: PhD, Medical Sciences - Physiology and Pharmacology (IDP), 2011, University of Florida

 The main focus of our laboratory is to elucidate transcriptional regulation of homeodomain transcription factor Nkx2.5 in the heart. For this study, we have focused… (more)

Subjects/Keywords: Cardiac output; Genetic loci; Heart; Heart ventricles; Journalism; Messenger RNA; Myocardium; Phosphorylation; Polymerase chain reaction; Promoter regions; cmlck  – nkx25

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APA (6th Edition):

Warren, S. A. (2011). Cardiac MLCK (cMLCK) and Its Role in Cardiac Function. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0043629

Chicago Manual of Style (16th Edition):

Warren, Soni A. “Cardiac MLCK (cMLCK) and Its Role in Cardiac Function.” 2011. Doctoral Dissertation, University of Florida. Accessed March 29, 2020. http://ufdc.ufl.edu/UFE0043629.

MLA Handbook (7th Edition):

Warren, Soni A. “Cardiac MLCK (cMLCK) and Its Role in Cardiac Function.” 2011. Web. 29 Mar 2020.

Vancouver:

Warren SA. Cardiac MLCK (cMLCK) and Its Role in Cardiac Function. [Internet] [Doctoral dissertation]. University of Florida; 2011. [cited 2020 Mar 29]. Available from: http://ufdc.ufl.edu/UFE0043629.

Council of Science Editors:

Warren SA. Cardiac MLCK (cMLCK) and Its Role in Cardiac Function. [Doctoral Dissertation]. University of Florida; 2011. Available from: http://ufdc.ufl.edu/UFE0043629


University of Alaska – Fairbanks

13. Oliver, Margaret G. The phylogenetics and evolutionary history of the northern latitude plant genus Therorhodion (Maxim.) small (Ericaceae) .

Degree: 2017, University of Alaska – Fairbanks

 Taxonomic uncertainty in the Arctic-alpine flowering plant genus Therorhodion (Maxim.) Small (Ericaceae) can be attributed to two distinctly different viewpoints representing the taxonomic diversity. Russian… (more)

Subjects/Keywords: Ericaceae; Arctic regions; Phylogeny; Evolution; Genetics; Genetic aspects

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APA (6th Edition):

Oliver, M. G. (2017). The phylogenetics and evolutionary history of the northern latitude plant genus Therorhodion (Maxim.) small (Ericaceae) . (Thesis). University of Alaska – Fairbanks. Retrieved from http://hdl.handle.net/11122/7897

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):

Oliver, Margaret G. “The phylogenetics and evolutionary history of the northern latitude plant genus Therorhodion (Maxim.) small (Ericaceae) .” 2017. Thesis, University of Alaska – Fairbanks. Accessed March 29, 2020. http://hdl.handle.net/11122/7897.

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

MLA Handbook (7th Edition):

Oliver, Margaret G. “The phylogenetics and evolutionary history of the northern latitude plant genus Therorhodion (Maxim.) small (Ericaceae) .” 2017. Web. 29 Mar 2020.

Vancouver:

Oliver MG. The phylogenetics and evolutionary history of the northern latitude plant genus Therorhodion (Maxim.) small (Ericaceae) . [Internet] [Thesis]. University of Alaska – Fairbanks; 2017. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/11122/7897.

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

Council of Science Editors:

Oliver MG. The phylogenetics and evolutionary history of the northern latitude plant genus Therorhodion (Maxim.) small (Ericaceae) . [Thesis]. University of Alaska – Fairbanks; 2017. Available from: http://hdl.handle.net/11122/7897

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


University of Cincinnati

14. Grote, Lauren E. Variability in Laboratory Reporting and Genetic Counseling for Regions of Homozygosity Associated With Parental Consanguinity/Incest.

Degree: MS, Medicine: Genetic Counseling, 2012, University of Cincinnati

 Purpose: SNP microarrays, used as a first tier test for individuals with unexplained developmental disabilities and/or congenital anomalies, are capable of detecting regions of homozygosity… (more)

Subjects/Keywords: Genetics; Regions of homozygosity; Microarray; Consanguinity; Incest; Heterozygosity; Genetic Counseling

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APA (6th Edition):

Grote, L. E. (2012). Variability in Laboratory Reporting and Genetic Counseling for Regions of Homozygosity Associated With Parental Consanguinity/Incest. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1337950675

Chicago Manual of Style (16th Edition):

Grote, Lauren E. “Variability in Laboratory Reporting and Genetic Counseling for Regions of Homozygosity Associated With Parental Consanguinity/Incest.” 2012. Masters Thesis, University of Cincinnati. Accessed March 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1337950675.

MLA Handbook (7th Edition):

Grote, Lauren E. “Variability in Laboratory Reporting and Genetic Counseling for Regions of Homozygosity Associated With Parental Consanguinity/Incest.” 2012. Web. 29 Mar 2020.

Vancouver:

Grote LE. Variability in Laboratory Reporting and Genetic Counseling for Regions of Homozygosity Associated With Parental Consanguinity/Incest. [Internet] [Masters thesis]. University of Cincinnati; 2012. [cited 2020 Mar 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1337950675.

Council of Science Editors:

Grote LE. Variability in Laboratory Reporting and Genetic Counseling for Regions of Homozygosity Associated With Parental Consanguinity/Incest. [Masters Thesis]. University of Cincinnati; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1337950675

15. Booker, Betty M. Analyzing DNA topology and transcription in Salmonella enterica serovar Typhimurium during dichotomous growth.

Degree: PhD, 2010, University of Alabama – Birmingham

The bacterial chromosome is dynamic. The principle goal of my research is to understand how DNA topology is altered by transcription in Salmonella enterica serovar… (more)

Subjects/Keywords: Chromosomes<; br>; DNA<; br>; RNA, Ribosomal<; br>; Salmonella typhimurium  – genetics<; br>; Transcription, Genetic

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APA (6th Edition):

Booker, B. M. (2010). Analyzing DNA topology and transcription in Salmonella enterica serovar Typhimurium during dichotomous growth. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,699

Chicago Manual of Style (16th Edition):

Booker, Betty M. “Analyzing DNA topology and transcription in Salmonella enterica serovar Typhimurium during dichotomous growth.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,699.

MLA Handbook (7th Edition):

Booker, Betty M. “Analyzing DNA topology and transcription in Salmonella enterica serovar Typhimurium during dichotomous growth.” 2010. Web. 29 Mar 2020.

Vancouver:

Booker BM. Analyzing DNA topology and transcription in Salmonella enterica serovar Typhimurium during dichotomous growth. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,699.

Council of Science Editors:

Booker BM. Analyzing DNA topology and transcription in Salmonella enterica serovar Typhimurium during dichotomous growth. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,699


Iowa State University

16. Sridharan, Krishnakumar. Computational analyses to identify and study cis-regulatory regions in eukaryotes.

Degree: 2012, Iowa State University

 Transcription is a vital and complicated process that is the first step leading to gene expression in eukaryotes. The initiation of transcription is controlled by… (more)

Subjects/Keywords: cis-regulatory regions; Computational tool design; Machine learning; Promoter region prediction; Structural features; Transcription; Bioinformatics; Genetics

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APA (6th Edition):

Sridharan, K. (2012). Computational analyses to identify and study cis-regulatory regions in eukaryotes. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/12845

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):

Sridharan, Krishnakumar. “Computational analyses to identify and study cis-regulatory regions in eukaryotes.” 2012. Thesis, Iowa State University. Accessed March 29, 2020. https://lib.dr.iastate.edu/etd/12845.

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

MLA Handbook (7th Edition):

Sridharan, Krishnakumar. “Computational analyses to identify and study cis-regulatory regions in eukaryotes.” 2012. Web. 29 Mar 2020.

Vancouver:

Sridharan K. Computational analyses to identify and study cis-regulatory regions in eukaryotes. [Internet] [Thesis]. Iowa State University; 2012. [cited 2020 Mar 29]. Available from: https://lib.dr.iastate.edu/etd/12845.

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

Council of Science Editors:

Sridharan K. Computational analyses to identify and study cis-regulatory regions in eukaryotes. [Thesis]. Iowa State University; 2012. Available from: https://lib.dr.iastate.edu/etd/12845

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

17. Dupraw, Diana Lee. Evolution and genetic diversity in streptococcus pneumoniae.

Degree: PhD, 2010, University of Alabama – Birmingham

The relative contributions of point mutations and intergenomic recombination via lateral gene transfer (LGT) determine the population structure and evolutionary style for a given bacterial… (more)

Subjects/Keywords: Evolution, Molecular<; br>; Gene Transfer, Horizontal<; br>; Genetic Variation<; br>; Pneumonia, Pneumococcal  – microbiology<; br>; Recombination, Genetic<; br>; Streptococcus pneumoniae  – genetics

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APA (6th Edition):

Dupraw, D. L. (2010). Evolution and genetic diversity in streptococcus pneumoniae. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1000

Chicago Manual of Style (16th Edition):

Dupraw, Diana Lee. “Evolution and genetic diversity in streptococcus pneumoniae.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1000.

MLA Handbook (7th Edition):

Dupraw, Diana Lee. “Evolution and genetic diversity in streptococcus pneumoniae.” 2010. Web. 29 Mar 2020.

Vancouver:

Dupraw DL. Evolution and genetic diversity in streptococcus pneumoniae. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1000.

Council of Science Editors:

Dupraw DL. Evolution and genetic diversity in streptococcus pneumoniae. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1000

18. Badiga, Suguna. Altered Dna Methylation Of Repetitive Elements May Explain The Modified Risk Of Cervical Intraepithelial Neoplasia (cin) Associated With Genetic Polymorphisms Of The Folate Metabolic Pathway In The Us Post Folic Acid Fortification Era.

Degree: PhD, 2011, University of Alabama – Birmingham

Despite the controversy regarding the adverse effects of exposure to higher folate concentrations on health outcomes particularly cancer, there has been paucity of research to… (more)

Subjects/Keywords: Cervical Intraepithelial Neoplasia – genetics.<; br>; DNA Methylation.<; br>; Diet<; br>; Folic Acid – blood<; br>; Genetic Variation – genetics.<; br>; Polymorphism, Genetic<; br>; Uterine Cervical Neoplasms – genetics.<; br>; Vitamin B 12 – blood.

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APA (6th Edition):

Badiga, S. (2011). Altered Dna Methylation Of Repetitive Elements May Explain The Modified Risk Of Cervical Intraepithelial Neoplasia (cin) Associated With Genetic Polymorphisms Of The Folate Metabolic Pathway In The Us Post Folic Acid Fortification Era. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1406

Chicago Manual of Style (16th Edition):

Badiga, Suguna. “Altered Dna Methylation Of Repetitive Elements May Explain The Modified Risk Of Cervical Intraepithelial Neoplasia (cin) Associated With Genetic Polymorphisms Of The Folate Metabolic Pathway In The Us Post Folic Acid Fortification Era.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1406.

MLA Handbook (7th Edition):

Badiga, Suguna. “Altered Dna Methylation Of Repetitive Elements May Explain The Modified Risk Of Cervical Intraepithelial Neoplasia (cin) Associated With Genetic Polymorphisms Of The Folate Metabolic Pathway In The Us Post Folic Acid Fortification Era.” 2011. Web. 29 Mar 2020.

Vancouver:

Badiga S. Altered Dna Methylation Of Repetitive Elements May Explain The Modified Risk Of Cervical Intraepithelial Neoplasia (cin) Associated With Genetic Polymorphisms Of The Folate Metabolic Pathway In The Us Post Folic Acid Fortification Era. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1406.

Council of Science Editors:

Badiga S. Altered Dna Methylation Of Repetitive Elements May Explain The Modified Risk Of Cervical Intraepithelial Neoplasia (cin) Associated With Genetic Polymorphisms Of The Folate Metabolic Pathway In The Us Post Folic Acid Fortification Era. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1406


University of Florida

19. Varn, Frederick. The Role of HMGA1 in the Recruitment of RNA Polymerase II to the Beta-Globin Gene Locus.

Degree: 2013, University of Florida

 Transcription complexes, composed of proteins including RNA polymerase, are recruited to the beginning of genes where RNA polymerase transcribes DNA into RNA, which serves as… (more)

Subjects/Keywords: Actins; Complementary DNA; DNA; Gene expression; Genes; Genetic loci; Oligomers; Polymerase chain reaction; Promoter regions; RNA; Genetic transcription; Globin genes; RNA polymerases; Transcription factors

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APA (6th Edition):

Varn, F. (2013). The Role of HMGA1 in the Recruitment of RNA Polymerase II to the Beta-Globin Gene Locus. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00061116

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):

Varn, Frederick. “The Role of HMGA1 in the Recruitment of RNA Polymerase II to the Beta-Globin Gene Locus.” 2013. Thesis, University of Florida. Accessed March 29, 2020. http://ufdc.ufl.edu/AA00061116.

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

MLA Handbook (7th Edition):

Varn, Frederick. “The Role of HMGA1 in the Recruitment of RNA Polymerase II to the Beta-Globin Gene Locus.” 2013. Web. 29 Mar 2020.

Vancouver:

Varn F. The Role of HMGA1 in the Recruitment of RNA Polymerase II to the Beta-Globin Gene Locus. [Internet] [Thesis]. University of Florida; 2013. [cited 2020 Mar 29]. Available from: http://ufdc.ufl.edu/AA00061116.

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

Council of Science Editors:

Varn F. The Role of HMGA1 in the Recruitment of RNA Polymerase II to the Beta-Globin Gene Locus. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00061116

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

20. Pickett, Brett E. The contribution of different mechanisms of viral sequence variation to the evolution of positive-sense single-stranded RNA viruses.

Degree: PhD, 2010, University of Alabama – Birmingham

The Flaviviridae family of positive-sense single-stranded RNA (+ssRNA) viruses includes viral taxa which greatly impact public health worldwide. To explore how the viruses within the… (more)

Subjects/Keywords: Computational Biology<; br>; Dengue Virus  – genetics<; br>; Hepacivirus  – genetics<; br>; Phylogeny<; br>; Polymorphism, Genetic<; br>; Recombination, Genetic<; br>; West Nile virus  – genetics

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APA (6th Edition):

Pickett, B. E. (2010). The contribution of different mechanisms of viral sequence variation to the evolution of positive-sense single-stranded RNA viruses. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,655

Chicago Manual of Style (16th Edition):

Pickett, Brett E. “The contribution of different mechanisms of viral sequence variation to the evolution of positive-sense single-stranded RNA viruses.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,655.

MLA Handbook (7th Edition):

Pickett, Brett E. “The contribution of different mechanisms of viral sequence variation to the evolution of positive-sense single-stranded RNA viruses.” 2010. Web. 29 Mar 2020.

Vancouver:

Pickett BE. The contribution of different mechanisms of viral sequence variation to the evolution of positive-sense single-stranded RNA viruses. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,655.

Council of Science Editors:

Pickett BE. The contribution of different mechanisms of viral sequence variation to the evolution of positive-sense single-stranded RNA viruses. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,655

21. 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 March 29, 2020. 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. 29 Mar 2020.

Vancouver:

Li X. Regulation of [beta]-catenin by Gli1 in epithelial transformation. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2006. [cited 2020 Mar 29]. 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

22. McCulley, Anna. Primer selection of E. coli tRNALys,3 by human immunodeficiency virus type-1.

Degree: PhD, 2007, University of Alabama – Birmingham

Human immunodeficiency virus (HIV) is the cause of acquired immunodeficiency syndrome (AIDS). HIV replication includes the notable process of reverse transcription, a conversion of RNA… (more)

Subjects/Keywords: Escherichia coli  – genetics <; br>; Escherichia coli  – metabolism <; br>; Genetic Complementation Test <; br>; HIV-1  – genetics <; br>; HIV-1  – physiology <; br>; RNA, Transfer, Lys  – genetics <; br>; RNA, Viral  – genetics <; br>; Selection (Genetics) <; br>; Virus Replication  – genetics

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APA (6th Edition):

McCulley, A. (2007). Primer selection of E. coli tRNALys,3 by human immunodeficiency virus type-1. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,184

Chicago Manual of Style (16th Edition):

McCulley, Anna. “Primer selection of E. coli tRNALys,3 by human immunodeficiency virus type-1.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,184.

MLA Handbook (7th Edition):

McCulley, Anna. “Primer selection of E. coli tRNALys,3 by human immunodeficiency virus type-1.” 2007. Web. 29 Mar 2020.

Vancouver:

McCulley A. Primer selection of E. coli tRNALys,3 by human immunodeficiency virus type-1. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,184.

Council of Science Editors:

McCulley A. Primer selection of E. coli tRNALys,3 by human immunodeficiency virus type-1. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,184

23. 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 March 29, 2020. 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. 29 Mar 2020.

Vancouver:

Tang Y. Modification of adenovirus capsid proteins for gene therapy applications. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2020 Mar 29]. 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

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 March 29, 2020. 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. 29 Mar 2020.

Vancouver:

Murakami M. Fiber modification of adenoviral vectors for cancer gene therapy. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Mar 29]. 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. Palmer, Matthew T. The influence of retroviral codon usage on the acquisition of the tRNA used to prime reverse transcription.

Degree: PhD, 2006, University of Alabama – Birmingham

An essential step in retrovirus replication is the conversion of the genomic-length viral RNA into a DNA copy, a reaction which is catalyzed by reverse… (more)

Subjects/Keywords: Leukemia Virus, Murine  – genetics <; br>; Leukemia Virus, Murine  – physiology <; br>; RNA  – genetics <; br>; RNA, Transfer, Lys  – genetics <; br>; RNA, Transfer, Phe  – genetics <; br>; RNA-Directed DNA Polymerase  – genetics <; br>; Transcription, Genetic <; br>; Virus Replication  – genetics

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APA (6th Edition):

Palmer, M. T. (2006). The influence of retroviral codon usage on the acquisition of the tRNA used to prime reverse transcription. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,149

Chicago Manual of Style (16th Edition):

Palmer, Matthew T. “The influence of retroviral codon usage on the acquisition of the tRNA used to prime reverse transcription.” 2006. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,149.

MLA Handbook (7th Edition):

Palmer, Matthew T. “The influence of retroviral codon usage on the acquisition of the tRNA used to prime reverse transcription.” 2006. Web. 29 Mar 2020.

Vancouver:

Palmer MT. The influence of retroviral codon usage on the acquisition of the tRNA used to prime reverse transcription. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2006. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,149.

Council of Science Editors:

Palmer MT. The influence of retroviral codon usage on the acquisition of the tRNA used to prime reverse transcription. [Doctoral Dissertation]. University of Alabama – Birmingham; 2006. Available from: http://contentdm.mhsl.uab.edu/u?/etd,149

26. Lai, Yi-Shin. Sox2/PARylated Parp1 complexes regulate pluripotency.

Degree: PhD, 2011, University of Alabama – Birmingham

Embryonic stem cells (ESCs) were first derived from the inner cell mass (ICM) of blastocyst-stage embryos. ESCs are distinguished from other cell types by their… (more)

Subjects/Keywords: Embryonic Stem Cells.<; br>; Fibroblasts – cytology<; br>; Genetic Vectors – genetics.<; br>; Lentivirus – genetics.<; br>; Nuclear Reprogramming – genetics.<; br>; Pluripotent Stem Cells – cytology.<; br>; Skin – cytology

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APA (6th Edition):

Lai, Y. (2011). Sox2/PARylated Parp1 complexes regulate pluripotency. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1361

Chicago Manual of Style (16th Edition):

Lai, Yi-Shin. “Sox2/PARylated Parp1 complexes regulate pluripotency.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed March 29, 2020. http://contentdm.mhsl.uab.edu/u?/etd,1361.

MLA Handbook (7th Edition):

Lai, Yi-Shin. “Sox2/PARylated Parp1 complexes regulate pluripotency.” 2011. Web. 29 Mar 2020.

Vancouver:

Lai Y. Sox2/PARylated Parp1 complexes regulate pluripotency. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2020 Mar 29]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1361.

Council of Science Editors:

Lai Y. Sox2/PARylated Parp1 complexes regulate pluripotency. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1361

27. Zhou, Qun-Yong. Molecular characterization of g-protein coupled receptors.

Degree: PhD, 1992, Oregon Health Sciences University

Subjects/Keywords: Receptors, Dopamine; Receptors, Purinergic; GTP-Binding Proteins; Promoter Regions, Genetic; Cloning, Molecular

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APA (6th Edition):

Zhou, Q. (1992). Molecular characterization of g-protein coupled receptors. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4CC0XSH ; http://digitalcommons.ohsu.edu/etd/1754

Chicago Manual of Style (16th Edition):

Zhou, Qun-Yong. “Molecular characterization of g-protein coupled receptors.” 1992. Doctoral Dissertation, Oregon Health Sciences University. Accessed March 29, 2020. doi:10.6083/M4CC0XSH ; http://digitalcommons.ohsu.edu/etd/1754.

MLA Handbook (7th Edition):

Zhou, Qun-Yong. “Molecular characterization of g-protein coupled receptors.” 1992. Web. 29 Mar 2020.

Vancouver:

Zhou Q. Molecular characterization of g-protein coupled receptors. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1992. [cited 2020 Mar 29]. Available from: doi:10.6083/M4CC0XSH ; http://digitalcommons.ohsu.edu/etd/1754.

Council of Science Editors:

Zhou Q. Molecular characterization of g-protein coupled receptors. [Doctoral Dissertation]. Oregon Health Sciences University; 1992. Available from: doi:10.6083/M4CC0XSH ; http://digitalcommons.ohsu.edu/etd/1754

28. Tajinda, Katsunori. Transcriptional regulatory mechanisms in IGF-I receptor gene expression : thesis.

Degree: MS, 1998, Oregon Health Sciences University

Subjects/Keywords: Receptor, IGF Type I; Transcription Factors; Gene Expression Regulation; Promoter Regions, Genetic

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APA (6th Edition):

Tajinda, K. (1998). Transcriptional regulatory mechanisms in IGF-I receptor gene expression : thesis. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4W37TJP ; http://digitalcommons.ohsu.edu/etd/2586

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):

Tajinda, Katsunori. “Transcriptional regulatory mechanisms in IGF-I receptor gene expression : thesis.” 1998. Thesis, Oregon Health Sciences University. Accessed March 29, 2020. doi:10.6083/M4W37TJP ; http://digitalcommons.ohsu.edu/etd/2586.

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

MLA Handbook (7th Edition):

Tajinda, Katsunori. “Transcriptional regulatory mechanisms in IGF-I receptor gene expression : thesis.” 1998. Web. 29 Mar 2020.

Vancouver:

Tajinda K. Transcriptional regulatory mechanisms in IGF-I receptor gene expression : thesis. [Internet] [Thesis]. Oregon Health Sciences University; 1998. [cited 2020 Mar 29]. Available from: doi:10.6083/M4W37TJP ; http://digitalcommons.ohsu.edu/etd/2586.

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

Council of Science Editors:

Tajinda K. Transcriptional regulatory mechanisms in IGF-I receptor gene expression : thesis. [Thesis]. Oregon Health Sciences University; 1998. Available from: doi:10.6083/M4W37TJP ; http://digitalcommons.ohsu.edu/etd/2586

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

29. Mills, Lisa Kathleen. Involvement of cellular transcription factors YY1 and SPX in regulating transactivation of herpes simplex virus type 1 γ₁ gene promoters.

Degree: PhD, 1996, Oregon Health Sciences University

Subjects/Keywords: Promoter Regions, Genetic; Simplexvirus; Sp1 Transcription Factor; Viral Fusion Proteins

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APA (6th Edition):

Mills, L. K. (1996). Involvement of cellular transcription factors YY1 and SPX in regulating transactivation of herpes simplex virus type 1 γ₁ gene promoters. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4BK19KH ; http://digitalcommons.ohsu.edu/etd/2714

Chicago Manual of Style (16th Edition):

Mills, Lisa Kathleen. “Involvement of cellular transcription factors YY1 and SPX in regulating transactivation of herpes simplex virus type 1 γ₁ gene promoters.” 1996. Doctoral Dissertation, Oregon Health Sciences University. Accessed March 29, 2020. doi:10.6083/M4BK19KH ; http://digitalcommons.ohsu.edu/etd/2714.

MLA Handbook (7th Edition):

Mills, Lisa Kathleen. “Involvement of cellular transcription factors YY1 and SPX in regulating transactivation of herpes simplex virus type 1 γ₁ gene promoters.” 1996. Web. 29 Mar 2020.

Vancouver:

Mills LK. Involvement of cellular transcription factors YY1 and SPX in regulating transactivation of herpes simplex virus type 1 γ₁ gene promoters. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1996. [cited 2020 Mar 29]. Available from: doi:10.6083/M4BK19KH ; http://digitalcommons.ohsu.edu/etd/2714.

Council of Science Editors:

Mills LK. Involvement of cellular transcription factors YY1 and SPX in regulating transactivation of herpes simplex virus type 1 γ₁ gene promoters. [Doctoral Dissertation]. Oregon Health Sciences University; 1996. Available from: doi:10.6083/M4BK19KH ; http://digitalcommons.ohsu.edu/etd/2714


University of Florida

30. Stees, Jared R. The Role of Noncoding RNA and Chromatin Structure in Regulating the Beta Globin Locus Control Region.

Degree: PhD, Genetics and Genomics, 2016, University of Florida

 The beta globin locus has been studied extensively over the years as a model for gene regulation and cis-acting domains. Much remains unclear including the… (more)

Subjects/Keywords: Chromatin; DNA; Erythroid cells; Gene expression; Genes; Genetic loci; Histones; Locus of control; Promoter regions; RNA; chromatin  – enhancer  – erna  – globin  – mapit  – rna

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

APA (6th Edition):

Stees, J. R. (2016). The Role of Noncoding RNA and Chromatin Structure in Regulating the Beta Globin Locus Control Region. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0049905

Chicago Manual of Style (16th Edition):

Stees, Jared R. “The Role of Noncoding RNA and Chromatin Structure in Regulating the Beta Globin Locus Control Region.” 2016. Doctoral Dissertation, University of Florida. Accessed March 29, 2020. http://ufdc.ufl.edu/UFE0049905.

MLA Handbook (7th Edition):

Stees, Jared R. “The Role of Noncoding RNA and Chromatin Structure in Regulating the Beta Globin Locus Control Region.” 2016. Web. 29 Mar 2020.

Vancouver:

Stees JR. The Role of Noncoding RNA and Chromatin Structure in Regulating the Beta Globin Locus Control Region. [Internet] [Doctoral dissertation]. University of Florida; 2016. [cited 2020 Mar 29]. Available from: http://ufdc.ufl.edu/UFE0049905.

Council of Science Editors:

Stees JR. The Role of Noncoding RNA and Chromatin Structure in Regulating the Beta Globin Locus Control Region. [Doctoral Dissertation]. University of Florida; 2016. Available from: http://ufdc.ufl.edu/UFE0049905

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