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You searched for subject:( Promoter Regions Genetic). Showing records 1 – 30 of 14386 total matches.

[1] [2] [3] [4] [5] … [480]

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University of Western Ontario

1. 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 22, 2019. 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. 22 Mar 2019.

Vancouver:

Rabbani M. Evolution of Mobile Promoters in Prokaryotic Genomes. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2019 Mar 22]. 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


University of Texas Southwestern Medical Center

2. 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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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

3. 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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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

4. 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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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

5. 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 22, 2019. http://ufdc.ufl.edu/UFE0043629.

MLA Handbook (7th Edition):

Warren, Soni A. “Cardiac MLCK (cMLCK) and Its Role in Cardiac Function.” 2011. Web. 22 Mar 2019.

Vancouver:

Warren SA. Cardiac MLCK (cMLCK) and Its Role in Cardiac Function. [Internet] [Doctoral dissertation]. University of Florida; 2011. [cited 2019 Mar 22]. 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 Florida

6. 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 22, 2019. 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. 22 Mar 2019.

Vancouver:

Barrow JJ. Analyzing Beta-Globin Cis-Regulatory Elements By Using Artificial DNA-Binding Domains. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2019 Mar 22]. 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

7. 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 (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 22, 2019. 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. 22 Mar 2019.

Vancouver:

Brown S. Functional genomics of LVIS_0853. [Internet] [Thesis]. University of Florida; 2010. [cited 2019 Mar 22]. 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

8. 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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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

9. 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 22, 2019. 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. 22 Mar 2019.

Vancouver:

Zhou Q. Molecular characterization of g-protein coupled receptors. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1992. [cited 2019 Mar 22]. 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

10. 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 22, 2019. 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. 22 Mar 2019.

Vancouver:

Tajinda K. Transcriptional regulatory mechanisms in IGF-I receptor gene expression : thesis. [Internet] [Thesis]. Oregon Health Sciences University; 1998. [cited 2019 Mar 22]. 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

11. 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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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

12. 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 (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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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

13. 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 22, 2019. 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. 22 Mar 2019.

Vancouver:

Yeo S. Transcriptional Regulation Of Gfap. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2019 Mar 22]. 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 Florida

14. Ingersoll, John Charles, 1953-. Transgenic expression of the alcohol dehydrogenase-1 gene of maize in sunflower.

Degree: 1990, University of Florida

Subjects/Keywords: Corn; DNA; Genes; Genetic mutation; Genetic vectors; Messenger RNA; Plasmids; Promoter regions; Sunflowers; Tumors

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APA (6th Edition):

Ingersoll, John Charles, 1. (1990). Transgenic expression of the alcohol dehydrogenase-1 gene of maize in sunflower. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00003747

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):

Ingersoll, John Charles, 1953-. “Transgenic expression of the alcohol dehydrogenase-1 gene of maize in sunflower.” 1990. Thesis, University of Florida. Accessed March 22, 2019. http://ufdc.ufl.edu/AA00003747.

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

MLA Handbook (7th Edition):

Ingersoll, John Charles, 1953-. “Transgenic expression of the alcohol dehydrogenase-1 gene of maize in sunflower.” 1990. Web. 22 Mar 2019.

Vancouver:

Ingersoll, John Charles 1. Transgenic expression of the alcohol dehydrogenase-1 gene of maize in sunflower. [Internet] [Thesis]. University of Florida; 1990. [cited 2019 Mar 22]. Available from: http://ufdc.ufl.edu/AA00003747.

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

Council of Science Editors:

Ingersoll, John Charles 1. Transgenic expression of the alcohol dehydrogenase-1 gene of maize in sunflower. [Thesis]. University of Florida; 1990. Available from: http://ufdc.ufl.edu/AA00003747

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


Duke University

15. West, AE. Mechanisms of specificity in neuronal activity-regulated gene transcription.

Degree: 2011, Duke University

 The brain is a highly adaptable organ that is capable of converting sensory information into changes in neuronal function. This plasticity allows behavior to be… (more)

Subjects/Keywords: Animals; Brain-Derived Neurotrophic Factor; Chromatin; Gene Expression Profiling; Gene Expression Regulation; Histones; Humans; Neuronal Plasticity; Neurons; Promoter Regions, Genetic; RNA Interference; Receptors, N-Methyl-D-Aspartate; Transcription Factors; Transcription, Genetic

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APA (6th Edition):

West, A. (2011). Mechanisms of specificity in neuronal activity-regulated gene transcription. (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5425

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):

West, AE. “Mechanisms of specificity in neuronal activity-regulated gene transcription. ” 2011. Thesis, Duke University. Accessed March 22, 2019. http://hdl.handle.net/10161/5425.

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

MLA Handbook (7th Edition):

West, AE. “Mechanisms of specificity in neuronal activity-regulated gene transcription. ” 2011. Web. 22 Mar 2019.

Vancouver:

West A. Mechanisms of specificity in neuronal activity-regulated gene transcription. [Internet] [Thesis]. Duke University; 2011. [cited 2019 Mar 22]. Available from: http://hdl.handle.net/10161/5425.

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

Council of Science Editors:

West A. Mechanisms of specificity in neuronal activity-regulated gene transcription. [Thesis]. Duke University; 2011. Available from: http://hdl.handle.net/10161/5425

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

16. 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 22, 2019. 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. 22 Mar 2019.

Vancouver:

Warram JM(M. Strategies for combined screening and imaging of breast cancer. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Mar 22]. 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

17. Laurance, Megan E. Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-I Tax, CRE-binding proteins, and CBP.

Degree: PhD, 1997, Oregon Health Sciences University

Subjects/Keywords: Promoter Regions, Genetic; Gene Expression Regulation, Viral; Human T-lymphotropic virus 1; Gene Products, tax; DNA-Binding Proteins; Protein Binding

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APA (6th Edition):

Laurance, M. E. (1997). Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-I Tax, CRE-binding proteins, and CBP. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4FQ9TT6 ; http://digitalcommons.ohsu.edu/etd/2628

Chicago Manual of Style (16th Edition):

Laurance, Megan E. “Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-I Tax, CRE-binding proteins, and CBP.” 1997. Doctoral Dissertation, Oregon Health Sciences University. Accessed March 22, 2019. doi:10.6083/M4FQ9TT6 ; http://digitalcommons.ohsu.edu/etd/2628.

MLA Handbook (7th Edition):

Laurance, Megan E. “Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-I Tax, CRE-binding proteins, and CBP.” 1997. Web. 22 Mar 2019.

Vancouver:

Laurance ME. Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-I Tax, CRE-binding proteins, and CBP. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1997. [cited 2019 Mar 22]. Available from: doi:10.6083/M4FQ9TT6 ; http://digitalcommons.ohsu.edu/etd/2628.

Council of Science Editors:

Laurance ME. Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-I Tax, CRE-binding proteins, and CBP. [Doctoral Dissertation]. Oregon Health Sciences University; 1997. Available from: doi:10.6083/M4FQ9TT6 ; http://digitalcommons.ohsu.edu/etd/2628

18. Adachi, Megumi. Molecular and biochemical characterization of paired-like homeodomain transcription factors, Arix.

Degree: PhD, 2001, Oregon Health Sciences University

Subjects/Keywords: Homeodomain Proteins; Transcription Factors; Promoter Regions, Genetic; Dopamine beta-Hydroxylase; Gene Expression Regulation, Enzymologic

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APA (6th Edition):

Adachi, M. (2001). Molecular and biochemical characterization of paired-like homeodomain transcription factors, Arix. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4SX6BGZ ; http://digitalcommons.ohsu.edu/etd/3230

Chicago Manual of Style (16th Edition):

Adachi, Megumi. “Molecular and biochemical characterization of paired-like homeodomain transcription factors, Arix.” 2001. Doctoral Dissertation, Oregon Health Sciences University. Accessed March 22, 2019. doi:10.6083/M4SX6BGZ ; http://digitalcommons.ohsu.edu/etd/3230.

MLA Handbook (7th Edition):

Adachi, Megumi. “Molecular and biochemical characterization of paired-like homeodomain transcription factors, Arix.” 2001. Web. 22 Mar 2019.

Vancouver:

Adachi M. Molecular and biochemical characterization of paired-like homeodomain transcription factors, Arix. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2001. [cited 2019 Mar 22]. Available from: doi:10.6083/M4SX6BGZ ; http://digitalcommons.ohsu.edu/etd/3230.

Council of Science Editors:

Adachi M. Molecular and biochemical characterization of paired-like homeodomain transcription factors, Arix. [Doctoral Dissertation]. Oregon Health Sciences University; 2001. Available from: doi:10.6083/M4SX6BGZ ; http://digitalcommons.ohsu.edu/etd/3230

19. Graves, David Craig. Analysis of three levels of regulation of expression of the human basic fibroblast growth factor gene : mRNA accumulation, upstream regulation, and basal promotion.

Degree: PhD, 1993, Oregon Health Sciences University

Subjects/Keywords: Fibroblasts; Fibroblast Growth Factor 2; Gene Expression Regulation; Phorbol Esters; Promoter Regions, Genetic; RNA, Messenger

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APA (6th Edition):

Graves, D. C. (1993). Analysis of three levels of regulation of expression of the human basic fibroblast growth factor gene : mRNA accumulation, upstream regulation, and basal promotion. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4DR2SQT ; http://digitalcommons.ohsu.edu/etd/2845

Chicago Manual of Style (16th Edition):

Graves, David Craig. “Analysis of three levels of regulation of expression of the human basic fibroblast growth factor gene : mRNA accumulation, upstream regulation, and basal promotion.” 1993. Doctoral Dissertation, Oregon Health Sciences University. Accessed March 22, 2019. doi:10.6083/M4DR2SQT ; http://digitalcommons.ohsu.edu/etd/2845.

MLA Handbook (7th Edition):

Graves, David Craig. “Analysis of three levels of regulation of expression of the human basic fibroblast growth factor gene : mRNA accumulation, upstream regulation, and basal promotion.” 1993. Web. 22 Mar 2019.

Vancouver:

Graves DC. Analysis of three levels of regulation of expression of the human basic fibroblast growth factor gene : mRNA accumulation, upstream regulation, and basal promotion. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1993. [cited 2019 Mar 22]. Available from: doi:10.6083/M4DR2SQT ; http://digitalcommons.ohsu.edu/etd/2845.

Council of Science Editors:

Graves DC. Analysis of three levels of regulation of expression of the human basic fibroblast growth factor gene : mRNA accumulation, upstream regulation, and basal promotion. [Doctoral Dissertation]. Oregon Health Sciences University; 1993. Available from: doi:10.6083/M4DR2SQT ; http://digitalcommons.ohsu.edu/etd/2845


University of Florida

20. Giordani, Nicole V. Regulation of the Herpes Simplex Virus Type-1 (HSV-1) Latency-Associated Transcript (LAT).

Degree: PhD, Medical Sciences - Immunology and Microbiology (IDP), 2007, University of Florida

 Herpes simplex virus type 1 (HSV-1) establishes latency in neurons until stimulated by stress to reactivate. The latency-associated transcript (LAT) region is the only portion… (more)

Subjects/Keywords: Chromatin; DNA; Genetic mutation; Genomes; Histones; Human herpesvirus 1; Infections; Promoter regions; Rabbits; RNA; hsv1, latency, reactivation, regulation

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APA (6th Edition):

Giordani, N. V. (2007). Regulation of the Herpes Simplex Virus Type-1 (HSV-1) Latency-Associated Transcript (LAT). (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0019662

Chicago Manual of Style (16th Edition):

Giordani, Nicole V. “Regulation of the Herpes Simplex Virus Type-1 (HSV-1) Latency-Associated Transcript (LAT).” 2007. Doctoral Dissertation, University of Florida. Accessed March 22, 2019. http://ufdc.ufl.edu/UFE0019662.

MLA Handbook (7th Edition):

Giordani, Nicole V. “Regulation of the Herpes Simplex Virus Type-1 (HSV-1) Latency-Associated Transcript (LAT).” 2007. Web. 22 Mar 2019.

Vancouver:

Giordani NV. Regulation of the Herpes Simplex Virus Type-1 (HSV-1) Latency-Associated Transcript (LAT). [Internet] [Doctoral dissertation]. University of Florida; 2007. [cited 2019 Mar 22]. Available from: http://ufdc.ufl.edu/UFE0019662.

Council of Science Editors:

Giordani NV. Regulation of the Herpes Simplex Virus Type-1 (HSV-1) Latency-Associated Transcript (LAT). [Doctoral Dissertation]. University of Florida; 2007. Available from: http://ufdc.ufl.edu/UFE0019662


University of Florida

21. 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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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


University of Cape Town

22. 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 22, 2019. 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. 22 Mar 2019.

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 2019 Mar 22]. 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

23. Montecino, Martin A. Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells.

Degree: Cell Biology, Radiology, 1995, U of Massachusetts : Med

  Transcription of the osteocalcin gene, which encodes a bone-specific 10 kDa protein, is controlled by the coordinated utilization of modularly organized basal and hormone-responsive… (more)

Subjects/Keywords: Osteocalcin; Promoter Regions; Rats; Gene Expression; Cells; Amino Acids, Peptides, and Proteins; Animal Experimentation and Research; Cells; Genetic Phenomena

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APA (6th Edition):

Montecino, M. A. (1995). Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/33

Chicago Manual of Style (16th Edition):

Montecino, Martin A. “Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells.” 1995. Doctoral Dissertation, U of Massachusetts : Med. Accessed March 22, 2019. https://escholarship.umassmed.edu/gsbs_diss/33.

MLA Handbook (7th Edition):

Montecino, Martin A. “Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells.” 1995. Web. 22 Mar 2019.

Vancouver:

Montecino MA. Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1995. [cited 2019 Mar 22]. Available from: https://escholarship.umassmed.edu/gsbs_diss/33.

Council of Science Editors:

Montecino MA. Chromatin Structure of the Rat Osteocalcin Gene Promoter in Bone-Derived Cells. [Doctoral Dissertation]. U of Massachusetts : Med; 1995. Available from: https://escholarship.umassmed.edu/gsbs_diss/33


Clemson University

24. Hussain, Murtaza Shabbir. Expanding the Genetic Toolbox to Improve Metabolic Engineering in the Industrial Oleaginous Yeast, Yarrowia lipolytica.

Degree: PhD, Chemical and Biomolecular Engineering, 2017, Clemson University

 The oleaginous yeast, Yarrowia lipolytica, is becoming a popular host for industrial biotechnology because of its ability to grow on non-conventional feedstocks and naturally accumulate… (more)

Subjects/Keywords: DNA Accessibility; Yarrowia lipolytica; fatty alcohol; genetic tools; hybrid promoter; Promoter Engineering

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APA (6th Edition):

Hussain, M. S. (2017). Expanding the Genetic Toolbox to Improve Metabolic Engineering in the Industrial Oleaginous Yeast, Yarrowia lipolytica. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/2048

Chicago Manual of Style (16th Edition):

Hussain, Murtaza Shabbir. “Expanding the Genetic Toolbox to Improve Metabolic Engineering in the Industrial Oleaginous Yeast, Yarrowia lipolytica.” 2017. Doctoral Dissertation, Clemson University. Accessed March 22, 2019. https://tigerprints.clemson.edu/all_dissertations/2048.

MLA Handbook (7th Edition):

Hussain, Murtaza Shabbir. “Expanding the Genetic Toolbox to Improve Metabolic Engineering in the Industrial Oleaginous Yeast, Yarrowia lipolytica.” 2017. Web. 22 Mar 2019.

Vancouver:

Hussain MS. Expanding the Genetic Toolbox to Improve Metabolic Engineering in the Industrial Oleaginous Yeast, Yarrowia lipolytica. [Internet] [Doctoral dissertation]. Clemson University; 2017. [cited 2019 Mar 22]. Available from: https://tigerprints.clemson.edu/all_dissertations/2048.

Council of Science Editors:

Hussain MS. Expanding the Genetic Toolbox to Improve Metabolic Engineering in the Industrial Oleaginous Yeast, Yarrowia lipolytica. [Doctoral Dissertation]. Clemson University; 2017. Available from: https://tigerprints.clemson.edu/all_dissertations/2048

25. Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, Koji. Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.).

Degree: 博士(歯学), 2015, Fukuoka Dental College / 福岡歯科大学

Reactive oxygen species (ROS) can cause severe damage to DNA, proteins and lipids in normal cells, contributing to carcinogenesis and various pathological conditions. While cellular… (more)

Subjects/Keywords: Cellar senescence; Reactive oxygen species; Cyclin-dependent kinase inhibitors; Normal human epidermal keratinocyte; Biological Markers; Cell Aging; Cell Line, Tumor; Cyclin-Dependent Kinase 4; Cyclin-Dependent Kinase Inhibitor p16; DNA Methylation; Epidermis; Epigenesis, Genetic; G1 Phase Cell Cycle Checkpoints; Humans; Hydrogen Peroxide; Keratinocytes; Organ Specificity; Promoter Regions, Genetic; Reactive Oxygen Species; Retinoblastoma Protein; Signal Transduction; beta-Galactosidase

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APA (6th Edition):

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, K. (2015). Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). (Thesis). Fukuoka Dental College / 福岡歯科大学. Retrieved from http://id.nii.ac.jp/1167/00000033/

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):

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, Koji. “Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.).” 2015. Thesis, Fukuoka Dental College / 福岡歯科大学. Accessed March 22, 2019. http://id.nii.ac.jp/1167/00000033/.

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

MLA Handbook (7th Edition):

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe, Koji. “Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.).” 2015. Web. 22 Mar 2019.

Vancouver:

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe K. Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). [Internet] [Thesis]. Fukuoka Dental College / 福岡歯科大学; 2015. [cited 2019 Mar 22]. Available from: http://id.nii.ac.jp/1167/00000033/.

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

Council of Science Editors:

Sasaki, Mina; Kajiya, Hiroshi; Ozeki, Satoru; Okabe K. Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). : Reactive oxygen species promotes cellular senescence in normal human epidermal keratinocytes through epigenetic regulation of p16(INK4a.). [Thesis]. Fukuoka Dental College / 福岡歯科大学; 2015. Available from: http://id.nii.ac.jp/1167/00000033/

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


University of Florida

26. Song, Jianing. The Initial Study of CsrA Involvement in Methionine Biosynthesis in Escherichia Coli K-12.

Degree: MS, Microbiology and Cell Science, 2014, University of Florida

 In Escherichia coli, CsrA RNA-binding protein posttranscriptionally regulates important cellular processes with multiple pleiotropic effects by binding to target genes and affecting the translation initiation… (more)

Subjects/Keywords: Bacteriology; Biochemistry; Biosynthesis; Escherichia coli; Microbiology; Plasmids; Promoter regions; Proteins; Repression; RNA; csra  – metj

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APA (6th Edition):

Song, J. (2014). The Initial Study of CsrA Involvement in Methionine Biosynthesis in Escherichia Coli K-12. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0047298

Chicago Manual of Style (16th Edition):

Song, Jianing. “The Initial Study of CsrA Involvement in Methionine Biosynthesis in Escherichia Coli K-12.” 2014. Masters Thesis, University of Florida. Accessed March 22, 2019. http://ufdc.ufl.edu/UFE0047298.

MLA Handbook (7th Edition):

Song, Jianing. “The Initial Study of CsrA Involvement in Methionine Biosynthesis in Escherichia Coli K-12.” 2014. Web. 22 Mar 2019.

Vancouver:

Song J. The Initial Study of CsrA Involvement in Methionine Biosynthesis in Escherichia Coli K-12. [Internet] [Masters thesis]. University of Florida; 2014. [cited 2019 Mar 22]. Available from: http://ufdc.ufl.edu/UFE0047298.

Council of Science Editors:

Song J. The Initial Study of CsrA Involvement in Methionine Biosynthesis in Escherichia Coli K-12. [Masters Thesis]. University of Florida; 2014. Available from: http://ufdc.ufl.edu/UFE0047298

27. Morton, Stephanie N. Investigation of the Role of Gata2 in the Activation of the Beta-Globin Locus Control Region during Early Erythropoiesis.

Degree: MS, Biochemistry and Molecular Biology, 2013, University of Florida

 The beta-globin locus control region (LCR) is a powerful enhancer region located 50 kilobasepairs upstream of the human beta-globin genes that has been shown to… (more)

Subjects/Keywords: Antibodies; Chromatin; DNA; Genetic loci; Histones; K562 cells; Promoter regions; RNA; Small interfering RNA; Transfection; brg1  – erythropoiesis  – gata2

…leads to removal of nucleosomes from the enhancer and promoter regions to which it is… …regulatory DNA region. Promoter and Enhancer Regions Several cis-regulatory DNA elements act in the… …Promoter Regions Promoter regions are a type of cis-regulatory DNA element located proximal to… …regions provide an added dissimilarity to promoter regions, as enhancers are marked by high… …opening the chromatin at promoter regions, positioning genes physically close to… 

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APA (6th Edition):

Morton, S. N. (2013). Investigation of the Role of Gata2 in the Activation of the Beta-Globin Locus Control Region during Early Erythropoiesis. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045520

Chicago Manual of Style (16th Edition):

Morton, Stephanie N. “Investigation of the Role of Gata2 in the Activation of the Beta-Globin Locus Control Region during Early Erythropoiesis.” 2013. Masters Thesis, University of Florida. Accessed March 22, 2019. http://ufdc.ufl.edu/UFE0045520.

MLA Handbook (7th Edition):

Morton, Stephanie N. “Investigation of the Role of Gata2 in the Activation of the Beta-Globin Locus Control Region during Early Erythropoiesis.” 2013. Web. 22 Mar 2019.

Vancouver:

Morton SN. Investigation of the Role of Gata2 in the Activation of the Beta-Globin Locus Control Region during Early Erythropoiesis. [Internet] [Masters thesis]. University of Florida; 2013. [cited 2019 Mar 22]. Available from: http://ufdc.ufl.edu/UFE0045520.

Council of Science Editors:

Morton SN. Investigation of the Role of Gata2 in the Activation of the Beta-Globin Locus Control Region during Early Erythropoiesis. [Masters Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045520


University of Florida

28. Lin, I-Ju. The Role of Calpain, USF, and TFII-I in Beta-Globin Gene Regulation.

Degree: PhD, Medical Sciences - Genetics (IDP), 2010, University of Florida

 Differentiation of erythroid cells is regulated by cell signaling pathways including those that change the intracellular concentration of calcium. Calcium-dependent proteases have been shown previously… (more)

Subjects/Keywords: Antibodies; Calcium; Chromatin; DNA; Erythroid cells; Gene expression; Genetic loci; Hemoglobins; Promoter regions; Proteins; adult, beta, biotinylation, calcium, calpain, calpeptin, cells, differentiation, efficient, entry, erythroid, erythropoiesis, factors, gene, globin, hemoglobinopathies, high, hsp70, in, influx, inhibition, inhibitor, locus, m, mass, mel, nfkappab, pathways, primary, progenitor, proteomics, regulation, signaling, spectrometry, streptavidin, tfii, throughput, topoisomerase, transcription, usf, vivo

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

APA (6th Edition):

Lin, I. (2010). The Role of Calpain, USF, and TFII-I in Beta-Globin Gene Regulation. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042457

Chicago Manual of Style (16th Edition):

Lin, I-Ju. “The Role of Calpain, USF, and TFII-I in Beta-Globin Gene Regulation.” 2010. Doctoral Dissertation, University of Florida. Accessed March 22, 2019. http://ufdc.ufl.edu/UFE0042457.

MLA Handbook (7th Edition):

Lin, I-Ju. “The Role of Calpain, USF, and TFII-I in Beta-Globin Gene Regulation.” 2010. Web. 22 Mar 2019.

Vancouver:

Lin I. The Role of Calpain, USF, and TFII-I in Beta-Globin Gene Regulation. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Mar 22]. Available from: http://ufdc.ufl.edu/UFE0042457.

Council of Science Editors:

Lin I. The Role of Calpain, USF, and TFII-I in Beta-Globin Gene Regulation. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042457


University of Florida

29. Benedict, Mark Q., 1951-. Heat-shock genes of the mosquito Anopheles albimanus Wiedemann.

Degree: 1990, University of Florida

Subjects/Keywords: Drosophila; Genes; Genetic loci; Heat shock proteins; Larvae; Mortality; Nucleotide sequences; Promoter regions; RNA; Shock heating; Entomology and Nematology thesis Ph. D

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APA (6th Edition):

Benedict, Mark Q., 1. (1990). Heat-shock genes of the mosquito Anopheles albimanus Wiedemann. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00029888

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):

Benedict, Mark Q., 1951-. “Heat-shock genes of the mosquito Anopheles albimanus Wiedemann.” 1990. Thesis, University of Florida. Accessed March 22, 2019. http://ufdc.ufl.edu/AA00029888.

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

MLA Handbook (7th Edition):

Benedict, Mark Q., 1951-. “Heat-shock genes of the mosquito Anopheles albimanus Wiedemann.” 1990. Web. 22 Mar 2019.

Vancouver:

Benedict, Mark Q. 1. Heat-shock genes of the mosquito Anopheles albimanus Wiedemann. [Internet] [Thesis]. University of Florida; 1990. [cited 2019 Mar 22]. Available from: http://ufdc.ufl.edu/AA00029888.

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

Council of Science Editors:

Benedict, Mark Q. 1. Heat-shock genes of the mosquito Anopheles albimanus Wiedemann. [Thesis]. University of Florida; 1990. Available from: http://ufdc.ufl.edu/AA00029888

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

30. Schoeben, Melissa A. Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans.

Degree: MSin Biology, Biology, 2017, Missouri State University

  The acetic acid bacterium Gluconobacter oxydans is an industrially valuable microorganism, particularly in the production of acetic acid, D-gluconic acid, ketogluconic acids, dihydroxyacetone, and… (more)

Subjects/Keywords: Gluconobacter oxydans; fluorescent reporter; inducible promoter; fusion protein; genetic tools; Microbiology

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

APA (6th Edition):

Schoeben, M. A. (2017). Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans. (Masters Thesis). Missouri State University. Retrieved from https://bearworks.missouristate.edu/theses/3117

Chicago Manual of Style (16th Edition):

Schoeben, Melissa A. “Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans.” 2017. Masters Thesis, Missouri State University. Accessed March 22, 2019. https://bearworks.missouristate.edu/theses/3117.

MLA Handbook (7th Edition):

Schoeben, Melissa A. “Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans.” 2017. Web. 22 Mar 2019.

Vancouver:

Schoeben MA. Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans. [Internet] [Masters thesis]. Missouri State University; 2017. [cited 2019 Mar 22]. Available from: https://bearworks.missouristate.edu/theses/3117.

Council of Science Editors:

Schoeben MA. Genetic Tools to Allow Efficient Gene and Protein Characterization of the Industrially Important Bacterium Gluconobacter Oxydans. [Masters Thesis]. Missouri State University; 2017. Available from: https://bearworks.missouristate.edu/theses/3117

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