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You searched for subject:(Protein Regulation). Showing records 1 – 30 of 466 total matches.

[1] [2] [3] [4] [5] … [16]

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University of Illinois – Chicago

1. Meydan, Fatma Sezen. Unconventional Translation Strategies That Diversify The Bacterial Proteome.

Degree: 2018, University of Illinois – Chicago

 A common rule in genetics is that each gene encodes a single protein. Although this is usually the case, organisms have evolved unique strategies allowing… (more)

Subjects/Keywords: protein synthesis; translation regulation

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APA (6th Edition):

Meydan, F. S. (2018). Unconventional Translation Strategies That Diversify The Bacterial Proteome. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22978

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):

Meydan, Fatma Sezen. “Unconventional Translation Strategies That Diversify The Bacterial Proteome.” 2018. Thesis, University of Illinois – Chicago. Accessed November 29, 2020. http://hdl.handle.net/10027/22978.

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

MLA Handbook (7th Edition):

Meydan, Fatma Sezen. “Unconventional Translation Strategies That Diversify The Bacterial Proteome.” 2018. Web. 29 Nov 2020.

Vancouver:

Meydan FS. Unconventional Translation Strategies That Diversify The Bacterial Proteome. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10027/22978.

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

Council of Science Editors:

Meydan FS. Unconventional Translation Strategies That Diversify The Bacterial Proteome. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/22978

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


University of Sydney

2. Szyszka, Taylor Nicole. Structural Studies of Bromodomain and Extra-Terminal Domain Protein BRD3 .

Degree: 2019, University of Sydney

 The work presented in this Thesis examines aspects of the molecular mechanisms underlying gene regulation, focusing on the bromodomain and extra-terminal domain (BET) protein family.… (more)

Subjects/Keywords: NMR; Protein; Structure; Gene Regulation

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APA (6th Edition):

Szyszka, T. N. (2019). Structural Studies of Bromodomain and Extra-Terminal Domain Protein BRD3 . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20221

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):

Szyszka, Taylor Nicole. “Structural Studies of Bromodomain and Extra-Terminal Domain Protein BRD3 .” 2019. Thesis, University of Sydney. Accessed November 29, 2020. http://hdl.handle.net/2123/20221.

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

MLA Handbook (7th Edition):

Szyszka, Taylor Nicole. “Structural Studies of Bromodomain and Extra-Terminal Domain Protein BRD3 .” 2019. Web. 29 Nov 2020.

Vancouver:

Szyszka TN. Structural Studies of Bromodomain and Extra-Terminal Domain Protein BRD3 . [Internet] [Thesis]. University of Sydney; 2019. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2123/20221.

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

Council of Science Editors:

Szyszka TN. Structural Studies of Bromodomain and Extra-Terminal Domain Protein BRD3 . [Thesis]. University of Sydney; 2019. Available from: http://hdl.handle.net/2123/20221

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


Penn State University

3. Liang, Xiaoying. Functional characterization of a Puf protein family member in malaria parasite Plasmodium falciparum.

Degree: 2017, Penn State University

Regulation of gene expression is important to cellular growth and differentiation of eukaryotes, as it plays key roles in determining the eventual expression levels and… (more)

Subjects/Keywords: Puf; RNA-binding protein; malaria; translational regulation

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APA (6th Edition):

Liang, X. (2017). Functional characterization of a Puf protein family member in malaria parasite Plasmodium falciparum. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14109xzl112

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):

Liang, Xiaoying. “Functional characterization of a Puf protein family member in malaria parasite Plasmodium falciparum.” 2017. Thesis, Penn State University. Accessed November 29, 2020. https://submit-etda.libraries.psu.edu/catalog/14109xzl112.

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

MLA Handbook (7th Edition):

Liang, Xiaoying. “Functional characterization of a Puf protein family member in malaria parasite Plasmodium falciparum.” 2017. Web. 29 Nov 2020.

Vancouver:

Liang X. Functional characterization of a Puf protein family member in malaria parasite Plasmodium falciparum. [Internet] [Thesis]. Penn State University; 2017. [cited 2020 Nov 29]. Available from: https://submit-etda.libraries.psu.edu/catalog/14109xzl112.

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

Council of Science Editors:

Liang X. Functional characterization of a Puf protein family member in malaria parasite Plasmodium falciparum. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14109xzl112

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


University of Manchester

4. Boukerrou, Ahmed Zakaria. Investigating the functional role of mammalian ribosomal protein uL22.

Degree: 2019, University of Manchester

 The ribosome is a ribonucleoprotein complex which translates mRNA into protein. During translation the nascent polypeptide chain passes through a confined exit tunnel environment which… (more)

Subjects/Keywords: Ribosome; Translation regulation; Unfolded protein response

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APA (6th Edition):

Boukerrou, A. Z. (2019). Investigating the functional role of mammalian ribosomal protein uL22. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318330

Chicago Manual of Style (16th Edition):

Boukerrou, Ahmed Zakaria. “Investigating the functional role of mammalian ribosomal protein uL22.” 2019. Doctoral Dissertation, University of Manchester. Accessed November 29, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318330.

MLA Handbook (7th Edition):

Boukerrou, Ahmed Zakaria. “Investigating the functional role of mammalian ribosomal protein uL22.” 2019. Web. 29 Nov 2020.

Vancouver:

Boukerrou AZ. Investigating the functional role of mammalian ribosomal protein uL22. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Nov 29]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318330.

Council of Science Editors:

Boukerrou AZ. Investigating the functional role of mammalian ribosomal protein uL22. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:318330


University of Edinburgh

5. Wells, Jonathan Nicholas. Regulatory mechanisms and biological implications of protein complex assembly.

Degree: PhD, 2018, University of Edinburgh

 Every living organism possesses a genome that contains within it a unique set of genes, a substantial number of which encode proteins. Over the last… (more)

Subjects/Keywords: protein complexes; assembly; gene regulation; proteomics; evolution

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APA (6th Edition):

Wells, J. N. (2018). Regulatory mechanisms and biological implications of protein complex assembly. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/31552

Chicago Manual of Style (16th Edition):

Wells, Jonathan Nicholas. “Regulatory mechanisms and biological implications of protein complex assembly.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed November 29, 2020. http://hdl.handle.net/1842/31552.

MLA Handbook (7th Edition):

Wells, Jonathan Nicholas. “Regulatory mechanisms and biological implications of protein complex assembly.” 2018. Web. 29 Nov 2020.

Vancouver:

Wells JN. Regulatory mechanisms and biological implications of protein complex assembly. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1842/31552.

Council of Science Editors:

Wells JN. Regulatory mechanisms and biological implications of protein complex assembly. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/31552


Hong Kong University of Science and Technology

6. Shan, Chuan. Identification of functional proteins in DNA damage checkpoint recovery.

Degree: 2013, Hong Kong University of Science and Technology

 The G2/M DNA damage checkpoint plays an important role in the maintenance of genome stability. It tightly controls the cell cycle machinery, and its deregulation… (more)

Subjects/Keywords: DNA damage ; Protein kinases ; Cell cycle ; Regulation

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APA (6th Edition):

Shan, C. (2013). Identification of functional proteins in DNA damage checkpoint recovery. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-80110 ; https://doi.org/10.14711/thesis-b1254488 ; http://repository.ust.hk/ir/bitstream/1783.1-80110/1/th_redirect.html

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):

Shan, Chuan. “Identification of functional proteins in DNA damage checkpoint recovery.” 2013. Thesis, Hong Kong University of Science and Technology. Accessed November 29, 2020. http://repository.ust.hk/ir/Record/1783.1-80110 ; https://doi.org/10.14711/thesis-b1254488 ; http://repository.ust.hk/ir/bitstream/1783.1-80110/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Shan, Chuan. “Identification of functional proteins in DNA damage checkpoint recovery.” 2013. Web. 29 Nov 2020.

Vancouver:

Shan C. Identification of functional proteins in DNA damage checkpoint recovery. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2013. [cited 2020 Nov 29]. Available from: http://repository.ust.hk/ir/Record/1783.1-80110 ; https://doi.org/10.14711/thesis-b1254488 ; http://repository.ust.hk/ir/bitstream/1783.1-80110/1/th_redirect.html.

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

Council of Science Editors:

Shan C. Identification of functional proteins in DNA damage checkpoint recovery. [Thesis]. Hong Kong University of Science and Technology; 2013. Available from: http://repository.ust.hk/ir/Record/1783.1-80110 ; https://doi.org/10.14711/thesis-b1254488 ; http://repository.ust.hk/ir/bitstream/1783.1-80110/1/th_redirect.html

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


University of Illinois – Urbana-Champaign

7. Henke, Sarah K. Regulatory function and interdomain communication of group II biotin protein ligases.

Degree: PhD, Microbiology, 2017, University of Illinois – Urbana-Champaign

 Biotin is a cofactor required for function of essential biotin dependent enzymes that are involved in metabolic processes including fatty acid biosynthesis, gluconeogenesis, and amino… (more)

Subjects/Keywords: Biotin; Biotin protein ligase; BirA; Transcriptional regulation

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APA (6th Edition):

Henke, S. K. (2017). Regulatory function and interdomain communication of group II biotin protein ligases. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/99277

Chicago Manual of Style (16th Edition):

Henke, Sarah K. “Regulatory function and interdomain communication of group II biotin protein ligases.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 29, 2020. http://hdl.handle.net/2142/99277.

MLA Handbook (7th Edition):

Henke, Sarah K. “Regulatory function and interdomain communication of group II biotin protein ligases.” 2017. Web. 29 Nov 2020.

Vancouver:

Henke SK. Regulatory function and interdomain communication of group II biotin protein ligases. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2142/99277.

Council of Science Editors:

Henke SK. Regulatory function and interdomain communication of group II biotin protein ligases. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/99277


Georgia Tech

8. Jung, Jeenah. Development of optical imaging method for detecting RNA-protein interactions.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2014, Georgia Tech

 The localization and translation of messenger ribonucleic acids (mRNAs) play crucial roles in cellular function and diseases, and are regulated by numerous RNA-binding proteins (RBPs)… (more)

Subjects/Keywords: RNA-protein interactions; Post-transcriptional regulation

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APA (6th Edition):

Jung, J. (2014). Development of optical imaging method for detecting RNA-protein interactions. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54278

Chicago Manual of Style (16th Edition):

Jung, Jeenah. “Development of optical imaging method for detecting RNA-protein interactions.” 2014. Doctoral Dissertation, Georgia Tech. Accessed November 29, 2020. http://hdl.handle.net/1853/54278.

MLA Handbook (7th Edition):

Jung, Jeenah. “Development of optical imaging method for detecting RNA-protein interactions.” 2014. Web. 29 Nov 2020.

Vancouver:

Jung J. Development of optical imaging method for detecting RNA-protein interactions. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1853/54278.

Council of Science Editors:

Jung J. Development of optical imaging method for detecting RNA-protein interactions. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54278


Louisiana State University

9. Evans, Alexandra Leigh. The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase.

Degree: PhD, Biochemistry, 2018, Louisiana State University

  Metabolic Regulation is a complex system used to control cellular metabolism in response to conditions in the cell’s environment. For most enzymes, the cell… (more)

Subjects/Keywords: Acetyl-CoA Carboxylase; Enzyme; Kinetics; Protein; Regulation

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APA (6th Edition):

Evans, A. L. (2018). The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase. (Doctoral Dissertation). Louisiana State University. Retrieved from https://digitalcommons.lsu.edu/gradschool_dissertations/4701

Chicago Manual of Style (16th Edition):

Evans, Alexandra Leigh. “The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase.” 2018. Doctoral Dissertation, Louisiana State University. Accessed November 29, 2020. https://digitalcommons.lsu.edu/gradschool_dissertations/4701.

MLA Handbook (7th Edition):

Evans, Alexandra Leigh. “The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase.” 2018. Web. 29 Nov 2020.

Vancouver:

Evans AL. The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase. [Internet] [Doctoral dissertation]. Louisiana State University; 2018. [cited 2020 Nov 29]. Available from: https://digitalcommons.lsu.edu/gradschool_dissertations/4701.

Council of Science Editors:

Evans AL. The Distinctive Regulatory Mechanisms of Bacterial Acetyl-CoA Carboxylase. [Doctoral Dissertation]. Louisiana State University; 2018. Available from: https://digitalcommons.lsu.edu/gradschool_dissertations/4701


University of Georgia

10. Maheshwari, Surabhi. Identification of conserved structural motifs associated with phosphorylation sites in kinases.

Degree: 2014, University of Georgia

 Background: Protein phosphorylation plays a crucial role in the regulation of several cellular processes. Protein kinases are enzymes that catalyze the event of phosphorylation and… (more)

Subjects/Keywords: phosphorylation; protein kinase; RD-pocket; regulation; allostery

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APA (6th Edition):

Maheshwari, S. (2014). Identification of conserved structural motifs associated with phosphorylation sites in kinases. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/28340

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):

Maheshwari, Surabhi. “Identification of conserved structural motifs associated with phosphorylation sites in kinases.” 2014. Thesis, University of Georgia. Accessed November 29, 2020. http://hdl.handle.net/10724/28340.

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

MLA Handbook (7th Edition):

Maheshwari, Surabhi. “Identification of conserved structural motifs associated with phosphorylation sites in kinases.” 2014. Web. 29 Nov 2020.

Vancouver:

Maheshwari S. Identification of conserved structural motifs associated with phosphorylation sites in kinases. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10724/28340.

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

Council of Science Editors:

Maheshwari S. Identification of conserved structural motifs associated with phosphorylation sites in kinases. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/28340

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


Virginia Tech

11. Ojani, Reyhaneh. Molecular mechanisms underlying Juvenile hormone (JH) signaling pathway.

Degree: PhD, Biochemistry, 2016, Virginia Tech

 Juvenile hormone (JH) is an important insect hormone that controls diverse biological processes in postembryonic development and adult reproduction. JH exerts its effects through the… (more)

Subjects/Keywords: Juvenile hormone; Protein kinase C; Gene regulation

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APA (6th Edition):

Ojani, R. (2016). Molecular mechanisms underlying Juvenile hormone (JH) signaling pathway. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/80342

Chicago Manual of Style (16th Edition):

Ojani, Reyhaneh. “Molecular mechanisms underlying Juvenile hormone (JH) signaling pathway.” 2016. Doctoral Dissertation, Virginia Tech. Accessed November 29, 2020. http://hdl.handle.net/10919/80342.

MLA Handbook (7th Edition):

Ojani, Reyhaneh. “Molecular mechanisms underlying Juvenile hormone (JH) signaling pathway.” 2016. Web. 29 Nov 2020.

Vancouver:

Ojani R. Molecular mechanisms underlying Juvenile hormone (JH) signaling pathway. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10919/80342.

Council of Science Editors:

Ojani R. Molecular mechanisms underlying Juvenile hormone (JH) signaling pathway. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/80342


Vanderbilt University

12. Meyer, Amanda N. Mechanisms of Transcription Activation by the DNA-binding Transfactor Repressor Activator Protein 1 (Rap1) Uncovered Using an Altered DNA-binding Specificity Variant.

Degree: PhD, Molecular Physiology and Biophysics, 2017, Vanderbilt University

 The enhancer DNA-binding transfactor Repressor activator protein 1 (Rap1) performs several essential cellular functions in the budding yeast Saccharomyces cerevisiae. These functions include regulation of… (more)

Subjects/Keywords: gene regulation; protein engineering; Saccharomyces cerevisiae; transcription regulation; yeast; transcription activator

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APA (6th Edition):

Meyer, A. N. (2017). Mechanisms of Transcription Activation by the DNA-binding Transfactor Repressor Activator Protein 1 (Rap1) Uncovered Using an Altered DNA-binding Specificity Variant. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12431

Chicago Manual of Style (16th Edition):

Meyer, Amanda N. “Mechanisms of Transcription Activation by the DNA-binding Transfactor Repressor Activator Protein 1 (Rap1) Uncovered Using an Altered DNA-binding Specificity Variant.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed November 29, 2020. http://hdl.handle.net/1803/12431.

MLA Handbook (7th Edition):

Meyer, Amanda N. “Mechanisms of Transcription Activation by the DNA-binding Transfactor Repressor Activator Protein 1 (Rap1) Uncovered Using an Altered DNA-binding Specificity Variant.” 2017. Web. 29 Nov 2020.

Vancouver:

Meyer AN. Mechanisms of Transcription Activation by the DNA-binding Transfactor Repressor Activator Protein 1 (Rap1) Uncovered Using an Altered DNA-binding Specificity Variant. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1803/12431.

Council of Science Editors:

Meyer AN. Mechanisms of Transcription Activation by the DNA-binding Transfactor Repressor Activator Protein 1 (Rap1) Uncovered Using an Altered DNA-binding Specificity Variant. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/12431


University of Waterloo

13. Lorv, Janet. Regulation of a cold inducible antifreeze protein in soil bacterium Pseudomonas putida GR12-2.

Degree: 2014, University of Waterloo

 In cold inhabiting bacteria, a commonly used strategy to combat freezing stress is the production of antifreeze proteins. These proteins assist in survival below 0… (more)

Subjects/Keywords: Protein regulation; Antifreeze protein; Plant growth promoting bacteria; Biology

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APA (6th Edition):

Lorv, J. (2014). Regulation of a cold inducible antifreeze protein in soil bacterium Pseudomonas putida GR12-2. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/8884

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):

Lorv, Janet. “Regulation of a cold inducible antifreeze protein in soil bacterium Pseudomonas putida GR12-2.” 2014. Thesis, University of Waterloo. Accessed November 29, 2020. http://hdl.handle.net/10012/8884.

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

MLA Handbook (7th Edition):

Lorv, Janet. “Regulation of a cold inducible antifreeze protein in soil bacterium Pseudomonas putida GR12-2.” 2014. Web. 29 Nov 2020.

Vancouver:

Lorv J. Regulation of a cold inducible antifreeze protein in soil bacterium Pseudomonas putida GR12-2. [Internet] [Thesis]. University of Waterloo; 2014. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/10012/8884.

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

Council of Science Editors:

Lorv J. Regulation of a cold inducible antifreeze protein in soil bacterium Pseudomonas putida GR12-2. [Thesis]. University of Waterloo; 2014. Available from: http://hdl.handle.net/10012/8884

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


Princeton University

14. Kobren, Shilpa Nadimpalli. Detecting and Analyzing Variation in Protein Interactions .

Degree: PhD, 2018, Princeton University

 Proteins carry out a dazzling multitude of functions by interacting with DNA, RNA, other proteins and various other molecules within our cells. Together these interactions… (more)

Subjects/Keywords: cancer genomics; gene regulation; protein domain; protein interaction interface

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APA (6th Edition):

Kobren, S. N. (2018). Detecting and Analyzing Variation in Protein Interactions . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01x059cb09d

Chicago Manual of Style (16th Edition):

Kobren, Shilpa Nadimpalli. “Detecting and Analyzing Variation in Protein Interactions .” 2018. Doctoral Dissertation, Princeton University. Accessed November 29, 2020. http://arks.princeton.edu/ark:/88435/dsp01x059cb09d.

MLA Handbook (7th Edition):

Kobren, Shilpa Nadimpalli. “Detecting and Analyzing Variation in Protein Interactions .” 2018. Web. 29 Nov 2020.

Vancouver:

Kobren SN. Detecting and Analyzing Variation in Protein Interactions . [Internet] [Doctoral dissertation]. Princeton University; 2018. [cited 2020 Nov 29]. Available from: http://arks.princeton.edu/ark:/88435/dsp01x059cb09d.

Council of Science Editors:

Kobren SN. Detecting and Analyzing Variation in Protein Interactions . [Doctoral Dissertation]. Princeton University; 2018. Available from: http://arks.princeton.edu/ark:/88435/dsp01x059cb09d


University of Toronto

15. Yang, Zhenglin. Expression of and Regulation by Nanos in Drosophila Early Embryos.

Degree: 2015, University of Toronto

Three categories of cytoplasmic post-transcriptional regulation that modulate mRNA stability, subcellular localization, and translation are coordinated to precisely control when and where a protein is… (more)

Subjects/Keywords: Drosophila; embryogenesis; local translational regulation; nanos; post-transcriptional regulation; RNA binding protein; 0307

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APA (6th Edition):

Yang, Z. (2015). Expression of and Regulation by Nanos in Drosophila Early Embryos. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/81011

Chicago Manual of Style (16th Edition):

Yang, Zhenglin. “Expression of and Regulation by Nanos in Drosophila Early Embryos.” 2015. Masters Thesis, University of Toronto. Accessed November 29, 2020. http://hdl.handle.net/1807/81011.

MLA Handbook (7th Edition):

Yang, Zhenglin. “Expression of and Regulation by Nanos in Drosophila Early Embryos.” 2015. Web. 29 Nov 2020.

Vancouver:

Yang Z. Expression of and Regulation by Nanos in Drosophila Early Embryos. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1807/81011.

Council of Science Editors:

Yang Z. Expression of and Regulation by Nanos in Drosophila Early Embryos. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/81011


Rice University

16. Kuypers, Brianna. Nanobody-mediated dynamic and spatial control of cellular proteins for mammalian gene circuit engineering.

Degree: PhD, Natural Sciences, 2019, Rice University

 Cellular information processing in mammalian cells relies on sophisticated and highly dynamic mechanisms. Unravelling these mechanisms remains a challenging endeavor and has limited de novo… (more)

Subjects/Keywords: nanobody; mammalian gene circuit; degradation; localization; orthogonal regulation; post-translational protein regulation

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APA (6th Edition):

Kuypers, B. (2019). Nanobody-mediated dynamic and spatial control of cellular proteins for mammalian gene circuit engineering. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/107736

Chicago Manual of Style (16th Edition):

Kuypers, Brianna. “Nanobody-mediated dynamic and spatial control of cellular proteins for mammalian gene circuit engineering.” 2019. Doctoral Dissertation, Rice University. Accessed November 29, 2020. http://hdl.handle.net/1911/107736.

MLA Handbook (7th Edition):

Kuypers, Brianna. “Nanobody-mediated dynamic and spatial control of cellular proteins for mammalian gene circuit engineering.” 2019. Web. 29 Nov 2020.

Vancouver:

Kuypers B. Nanobody-mediated dynamic and spatial control of cellular proteins for mammalian gene circuit engineering. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1911/107736.

Council of Science Editors:

Kuypers B. Nanobody-mediated dynamic and spatial control of cellular proteins for mammalian gene circuit engineering. [Doctoral Dissertation]. Rice University; 2019. Available from: http://hdl.handle.net/1911/107736


University of South Carolina

17. Bequette, Carlton James. MAP Kinase Signaling in Plant Responses to Biotic Stress.

Degree: PhD, Biological Sciences, 2015, University of South Carolina

  Plants must be able to perceive and properly respond to a multitude of environmental conditions and produce appropriate cellular responses for optimal growth and… (more)

Subjects/Keywords: Biology; Life Sciences; Mitogen-activated protein kinase; MAPK; regulation of cell death; multi-protein complex; negative regulation of MAPKs; stress responses

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APA (6th Edition):

Bequette, C. J. (2015). MAP Kinase Signaling in Plant Responses to Biotic Stress. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/3142

Chicago Manual of Style (16th Edition):

Bequette, Carlton James. “MAP Kinase Signaling in Plant Responses to Biotic Stress.” 2015. Doctoral Dissertation, University of South Carolina. Accessed November 29, 2020. https://scholarcommons.sc.edu/etd/3142.

MLA Handbook (7th Edition):

Bequette, Carlton James. “MAP Kinase Signaling in Plant Responses to Biotic Stress.” 2015. Web. 29 Nov 2020.

Vancouver:

Bequette CJ. MAP Kinase Signaling in Plant Responses to Biotic Stress. [Internet] [Doctoral dissertation]. University of South Carolina; 2015. [cited 2020 Nov 29]. Available from: https://scholarcommons.sc.edu/etd/3142.

Council of Science Editors:

Bequette CJ. MAP Kinase Signaling in Plant Responses to Biotic Stress. [Doctoral Dissertation]. University of South Carolina; 2015. Available from: https://scholarcommons.sc.edu/etd/3142


University of Cincinnati

18. Gow, Chien-Hung, M.D. Novel mechanisms of transcriptional regulation by leukemia fusion proteins.

Degree: PhD, Medicine: Cancer and Cell Biology, 2014, University of Cincinnati

 Transcription factors and chromatin structure are master regulators of homeostasis during hematopoiesis. Regulatory genes for each stage of hematopoiesis are activated or silenced in a… (more)

Subjects/Keywords: Oncology; transcriptional regulation; leukemia fusion protein; E-protein; E2A-Pbx1; AML1-ETO; HDAC3

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APA (6th Edition):

Gow, Chien-Hung, M. D. (2014). Novel mechanisms of transcriptional regulation by leukemia fusion proteins. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980

Chicago Manual of Style (16th Edition):

Gow, Chien-Hung, M D. “Novel mechanisms of transcriptional regulation by leukemia fusion proteins.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed November 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980.

MLA Handbook (7th Edition):

Gow, Chien-Hung, M D. “Novel mechanisms of transcriptional regulation by leukemia fusion proteins.” 2014. Web. 29 Nov 2020.

Vancouver:

Gow, Chien-Hung MD. Novel mechanisms of transcriptional regulation by leukemia fusion proteins. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2020 Nov 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980.

Council of Science Editors:

Gow, Chien-Hung MD. Novel mechanisms of transcriptional regulation by leukemia fusion proteins. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1394724980


University of Cincinnati

19. Zhang, Minlu. Discovery and Analysis of Patterns in Molecular Networks: Link Prediction, Network Analysis, and Applications to Novel Drug Target Discovery.

Degree: PhD, Engineering and Applied Science: Computer Science and Engineering, 2012, University of Cincinnati

  One of the most challenging problems in the post-genomic era for computer scientists and bioinformaticians is to identify meaningful patterns from a huge amount… (more)

Subjects/Keywords: Computer Science; network analysis; link prediction; transcriptional regulation; orphan disease; rare disease; protein-protein interaction

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APA (6th Edition):

Zhang, M. (2012). Discovery and Analysis of Patterns in Molecular Networks: Link Prediction, Network Analysis, and Applications to Novel Drug Target Discovery. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1330024618

Chicago Manual of Style (16th Edition):

Zhang, Minlu. “Discovery and Analysis of Patterns in Molecular Networks: Link Prediction, Network Analysis, and Applications to Novel Drug Target Discovery.” 2012. Doctoral Dissertation, University of Cincinnati. Accessed November 29, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1330024618.

MLA Handbook (7th Edition):

Zhang, Minlu. “Discovery and Analysis of Patterns in Molecular Networks: Link Prediction, Network Analysis, and Applications to Novel Drug Target Discovery.” 2012. Web. 29 Nov 2020.

Vancouver:

Zhang M. Discovery and Analysis of Patterns in Molecular Networks: Link Prediction, Network Analysis, and Applications to Novel Drug Target Discovery. [Internet] [Doctoral dissertation]. University of Cincinnati; 2012. [cited 2020 Nov 29]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1330024618.

Council of Science Editors:

Zhang M. Discovery and Analysis of Patterns in Molecular Networks: Link Prediction, Network Analysis, and Applications to Novel Drug Target Discovery. [Doctoral Dissertation]. University of Cincinnati; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1330024618


Princeton University

20. Wetzel, Joshua. Structure-aware Approaches for Deciphering Sequence-specific Protein-DNA Interactions .

Degree: PhD, 2019, Princeton University

 Interactions between proteins and specific genomic loci are critical to the proper functioning of all cells. The ability of a DNA-binding protein (DBP) to distinguish… (more)

Subjects/Keywords: DNA-binding; gene regulation; protein-DNA interaction; protein structure; transcription factor; zinc finger

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APA (6th Edition):

Wetzel, J. (2019). Structure-aware Approaches for Deciphering Sequence-specific Protein-DNA Interactions . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01x346d6976

Chicago Manual of Style (16th Edition):

Wetzel, Joshua. “Structure-aware Approaches for Deciphering Sequence-specific Protein-DNA Interactions .” 2019. Doctoral Dissertation, Princeton University. Accessed November 29, 2020. http://arks.princeton.edu/ark:/88435/dsp01x346d6976.

MLA Handbook (7th Edition):

Wetzel, Joshua. “Structure-aware Approaches for Deciphering Sequence-specific Protein-DNA Interactions .” 2019. Web. 29 Nov 2020.

Vancouver:

Wetzel J. Structure-aware Approaches for Deciphering Sequence-specific Protein-DNA Interactions . [Internet] [Doctoral dissertation]. Princeton University; 2019. [cited 2020 Nov 29]. Available from: http://arks.princeton.edu/ark:/88435/dsp01x346d6976.

Council of Science Editors:

Wetzel J. Structure-aware Approaches for Deciphering Sequence-specific Protein-DNA Interactions . [Doctoral Dissertation]. Princeton University; 2019. Available from: http://arks.princeton.edu/ark:/88435/dsp01x346d6976


University of Michigan

21. Blewett, Nathan Hans. Identification of the Mechanisms of mRNA Regulation by PUF Proteins.

Degree: PhD, Cellular & Molecular Biology, 2013, University of Michigan

 PUF proteins are conserved RNA-binding proteins that regulate mRNAs through sequence-specific binding. PUFs play integral roles in important biological processes including: development, fertility, and synaptic… (more)

Subjects/Keywords: RNA Binding Protein; PUF Protein; EIF-4E Binding Protein; Post-transcriptional MRNA Regulation; Biological Chemistry; Health Sciences

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APA (6th Edition):

Blewett, N. H. (2013). Identification of the Mechanisms of mRNA Regulation by PUF Proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/98060

Chicago Manual of Style (16th Edition):

Blewett, Nathan Hans. “Identification of the Mechanisms of mRNA Regulation by PUF Proteins.” 2013. Doctoral Dissertation, University of Michigan. Accessed November 29, 2020. http://hdl.handle.net/2027.42/98060.

MLA Handbook (7th Edition):

Blewett, Nathan Hans. “Identification of the Mechanisms of mRNA Regulation by PUF Proteins.” 2013. Web. 29 Nov 2020.

Vancouver:

Blewett NH. Identification of the Mechanisms of mRNA Regulation by PUF Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2027.42/98060.

Council of Science Editors:

Blewett NH. Identification of the Mechanisms of mRNA Regulation by PUF Proteins. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/98060


Georgia State University

22. Liu, Fange. A Structural and Mechanistic Study of Two Members of Cupin Family Protein.

Degree: PhD, Chemistry, 2013, Georgia State University

  is a functionally diverse large group of proteins sharing a jelly roll β-barrel fold. An enzymatic member 3-hydroxyanthranilate-3,4-dioxygenase (HAO) and a non-enzymatic member pirin,… (more)

Subjects/Keywords: Metalloprotein; Oxygen activation; Catalytic mechanism; Protein-protein and Protein- DNA interactions; Signaling transduction activation; Regulation of gene transcription

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APA (6th Edition):

Liu, F. (2013). A Structural and Mechanistic Study of Two Members of Cupin Family Protein. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/79

Chicago Manual of Style (16th Edition):

Liu, Fange. “A Structural and Mechanistic Study of Two Members of Cupin Family Protein.” 2013. Doctoral Dissertation, Georgia State University. Accessed November 29, 2020. https://scholarworks.gsu.edu/chemistry_diss/79.

MLA Handbook (7th Edition):

Liu, Fange. “A Structural and Mechanistic Study of Two Members of Cupin Family Protein.” 2013. Web. 29 Nov 2020.

Vancouver:

Liu F. A Structural and Mechanistic Study of Two Members of Cupin Family Protein. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2020 Nov 29]. Available from: https://scholarworks.gsu.edu/chemistry_diss/79.

Council of Science Editors:

Liu F. A Structural and Mechanistic Study of Two Members of Cupin Family Protein. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/chemistry_diss/79


Penn State University

23. Chan, Yan Mei. Functional Regulation and Protein Structural Dynamics of Poliovirus 3c Protease.

Degree: 2015, Penn State University

 Viruses employ numerous strategies to maximize the use of their compact genomes. These strategies include the generation of multifunctional proteins, and post-translational processing to produce… (more)

Subjects/Keywords: Viruses; Poliovirus; Structural Dynamics; Functional Regulation; 3C Protease; Protein NMR

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APA (6th Edition):

Chan, Y. M. (2015). Functional Regulation and Protein Structural Dynamics of Poliovirus 3c Protease. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/26301

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):

Chan, Yan Mei. “Functional Regulation and Protein Structural Dynamics of Poliovirus 3c Protease.” 2015. Thesis, Penn State University. Accessed November 29, 2020. https://submit-etda.libraries.psu.edu/catalog/26301.

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

MLA Handbook (7th Edition):

Chan, Yan Mei. “Functional Regulation and Protein Structural Dynamics of Poliovirus 3c Protease.” 2015. Web. 29 Nov 2020.

Vancouver:

Chan YM. Functional Regulation and Protein Structural Dynamics of Poliovirus 3c Protease. [Internet] [Thesis]. Penn State University; 2015. [cited 2020 Nov 29]. Available from: https://submit-etda.libraries.psu.edu/catalog/26301.

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

Council of Science Editors:

Chan YM. Functional Regulation and Protein Structural Dynamics of Poliovirus 3c Protease. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/26301

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


Penn State University

24. Reja, Rohit. Understanding Molecular Mechanisms of Gene Regulation using High Resolution ChIP-exo.

Degree: 2016, Penn State University

 A long-standing major question in biology is to understand the molecular mechanisms that govern the process of gene regulation in response to cellular signaling. Single… (more)

Subjects/Keywords: ChIP-exo; gene regulation; ribosomal protein genes; architecture

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APA (6th Edition):

Reja, R. (2016). Understanding Molecular Mechanisms of Gene Regulation using High Resolution ChIP-exo. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/28600

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):

Reja, Rohit. “Understanding Molecular Mechanisms of Gene Regulation using High Resolution ChIP-exo.” 2016. Thesis, Penn State University. Accessed November 29, 2020. https://submit-etda.libraries.psu.edu/catalog/28600.

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

MLA Handbook (7th Edition):

Reja, Rohit. “Understanding Molecular Mechanisms of Gene Regulation using High Resolution ChIP-exo.” 2016. Web. 29 Nov 2020.

Vancouver:

Reja R. Understanding Molecular Mechanisms of Gene Regulation using High Resolution ChIP-exo. [Internet] [Thesis]. Penn State University; 2016. [cited 2020 Nov 29]. Available from: https://submit-etda.libraries.psu.edu/catalog/28600.

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

Council of Science Editors:

Reja R. Understanding Molecular Mechanisms of Gene Regulation using High Resolution ChIP-exo. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/28600

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


McMaster University

25. Kuryllo, Kacper. Detecting RNA Regulatory Interactions in Bacterial Cells.

Degree: PhD, 2014, McMaster University

Non-coding RNAs are involved in the regulation of most major cellular process in Escherichia coli. With current technologies, many of these molecules have been identified;… (more)

Subjects/Keywords: RNA; gene regulation; sRNA; riboswitch; biosensor; fluorescent protein; GFP; Escherichia coli

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APA (6th Edition):

Kuryllo, K. (2014). Detecting RNA Regulatory Interactions in Bacterial Cells. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/16296

Chicago Manual of Style (16th Edition):

Kuryllo, Kacper. “Detecting RNA Regulatory Interactions in Bacterial Cells.” 2014. Doctoral Dissertation, McMaster University. Accessed November 29, 2020. http://hdl.handle.net/11375/16296.

MLA Handbook (7th Edition):

Kuryllo, Kacper. “Detecting RNA Regulatory Interactions in Bacterial Cells.” 2014. Web. 29 Nov 2020.

Vancouver:

Kuryllo K. Detecting RNA Regulatory Interactions in Bacterial Cells. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/11375/16296.

Council of Science Editors:

Kuryllo K. Detecting RNA Regulatory Interactions in Bacterial Cells. [Doctoral Dissertation]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/16296


Purdue University

26. Zeng, Wenjie. Elucidating The Mechanism Of Phenylpropanoid Regulation By The Arabidopsis Mediator Complex.

Degree: MS, Biochemistry, 2014, Purdue University

  The Mediator complex is a multi-protein co-regulator of eukaryotic transcription which plays a role in the expression of many, if not most, genes of… (more)

Subjects/Keywords: Pure sciences; Mediators; Phenylpropanoids; Protein purification; Specialized metabolism; Transcription regulation; Chemistry

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APA (6th Edition):

Zeng, W. (2014). Elucidating The Mechanism Of Phenylpropanoid Regulation By The Arabidopsis Mediator Complex. (Thesis). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_theses/400

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):

Zeng, Wenjie. “Elucidating The Mechanism Of Phenylpropanoid Regulation By The Arabidopsis Mediator Complex.” 2014. Thesis, Purdue University. Accessed November 29, 2020. http://docs.lib.purdue.edu/open_access_theses/400.

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

MLA Handbook (7th Edition):

Zeng, Wenjie. “Elucidating The Mechanism Of Phenylpropanoid Regulation By The Arabidopsis Mediator Complex.” 2014. Web. 29 Nov 2020.

Vancouver:

Zeng W. Elucidating The Mechanism Of Phenylpropanoid Regulation By The Arabidopsis Mediator Complex. [Internet] [Thesis]. Purdue University; 2014. [cited 2020 Nov 29]. Available from: http://docs.lib.purdue.edu/open_access_theses/400.

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

Council of Science Editors:

Zeng W. Elucidating The Mechanism Of Phenylpropanoid Regulation By The Arabidopsis Mediator Complex. [Thesis]. Purdue University; 2014. Available from: http://docs.lib.purdue.edu/open_access_theses/400

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


University of Toronto

27. Claridge, P. Colin. Overexpressing Gαs in Osteoblasts in vitro and in vivo: Effects on Basal and PTH-Stimulated Gene Expression.

Degree: 2014, University of Toronto

Previous work in our laboratory showed altered signaling through the parathyroid hormone (PTH) receptor when Gas was overexpressed in osteoblasts. To examine the effect of… (more)

Subjects/Keywords: Gas; Gene regulation; G protein; Osteoblast; Parathyroid hormone; 0419

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APA (6th Edition):

Claridge, P. C. (2014). Overexpressing Gαs in Osteoblasts in vitro and in vivo: Effects on Basal and PTH-Stimulated Gene Expression. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68552

Chicago Manual of Style (16th Edition):

Claridge, P Colin. “Overexpressing Gαs in Osteoblasts in vitro and in vivo: Effects on Basal and PTH-Stimulated Gene Expression.” 2014. Masters Thesis, University of Toronto. Accessed November 29, 2020. http://hdl.handle.net/1807/68552.

MLA Handbook (7th Edition):

Claridge, P Colin. “Overexpressing Gαs in Osteoblasts in vitro and in vivo: Effects on Basal and PTH-Stimulated Gene Expression.” 2014. Web. 29 Nov 2020.

Vancouver:

Claridge PC. Overexpressing Gαs in Osteoblasts in vitro and in vivo: Effects on Basal and PTH-Stimulated Gene Expression. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/1807/68552.

Council of Science Editors:

Claridge PC. Overexpressing Gαs in Osteoblasts in vitro and in vivo: Effects on Basal and PTH-Stimulated Gene Expression. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68552


Texas Medical Center

28. Hart, Anne. ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA.

Degree: PhD, 2011, Texas Medical Center

  Enhanced expression of the presynaptic protein synapsin has been correlated with certain forms of long-term plasticity and learning and memory. However, the regulation and… (more)

Subjects/Keywords: CREB; gene regulation; plasticity; synaptic vesicle protein; memory; Neuroscience and Neurobiology

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APA (6th Edition):

Hart, A. (2011). ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/148

Chicago Manual of Style (16th Edition):

Hart, Anne. “ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA.” 2011. Doctoral Dissertation, Texas Medical Center. Accessed November 29, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/148.

MLA Handbook (7th Edition):

Hart, Anne. “ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA.” 2011. Web. 29 Nov 2020.

Vancouver:

Hart A. ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA. [Internet] [Doctoral dissertation]. Texas Medical Center; 2011. [cited 2020 Nov 29]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/148.

Council of Science Editors:

Hart A. ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA. [Doctoral Dissertation]. Texas Medical Center; 2011. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/148


University of Texas Southwestern Medical Center

29. Hooks, Jared Cole. Regulation of the Tumor Suppressor ARF by TGFβ in Human Cancer Cells.

Degree: 2016, University of Texas Southwestern Medical Center

 Since its discovery, p14ARF (p19Arf in mice) has been shown to be an important regulator of the cell cycle, carrying out this function through p53-dependent… (more)

Subjects/Keywords: Gene Expression Regulation; Transforming Growth Factor beta; Tumor Suppressor Protein p14ARF

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APA (6th Edition):

Hooks, J. C. (2016). Regulation of the Tumor Suppressor ARF by TGFβ in Human Cancer Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6143

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):

Hooks, Jared Cole. “Regulation of the Tumor Suppressor ARF by TGFβ in Human Cancer Cells.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed November 29, 2020. http://hdl.handle.net/2152.5/6143.

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

MLA Handbook (7th Edition):

Hooks, Jared Cole. “Regulation of the Tumor Suppressor ARF by TGFβ in Human Cancer Cells.” 2016. Web. 29 Nov 2020.

Vancouver:

Hooks JC. Regulation of the Tumor Suppressor ARF by TGFβ in Human Cancer Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2152.5/6143.

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

Council of Science Editors:

Hooks JC. Regulation of the Tumor Suppressor ARF by TGFβ in Human Cancer Cells. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/6143

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

30. Luethy, Paul Michael. Signals and Sensory Mechanisms that Impact Campylobacter jejuni-Host Interactions.

Degree: 2015, University of Texas Southwestern Medical Center

 Campylobacter jejuni is a leading cause of bacterial diarrheal disease worldwide and a frequent commensal organism of the intestinal tract of poultry and other agriculturally-important… (more)

Subjects/Keywords: Campylobacter jejuni; Gene Expression Regulation, Bacterial; Protein Kinases; Regulon; Transcription Factors

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APA (6th Edition):

Luethy, P. M. (2015). Signals and Sensory Mechanisms that Impact Campylobacter jejuni-Host Interactions. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4202

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):

Luethy, Paul Michael. “Signals and Sensory Mechanisms that Impact Campylobacter jejuni-Host Interactions.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed November 29, 2020. http://hdl.handle.net/2152.5/4202.

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

MLA Handbook (7th Edition):

Luethy, Paul Michael. “Signals and Sensory Mechanisms that Impact Campylobacter jejuni-Host Interactions.” 2015. Web. 29 Nov 2020.

Vancouver:

Luethy PM. Signals and Sensory Mechanisms that Impact Campylobacter jejuni-Host Interactions. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Nov 29]. Available from: http://hdl.handle.net/2152.5/4202.

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

Council of Science Editors:

Luethy PM. Signals and Sensory Mechanisms that Impact Campylobacter jejuni-Host Interactions. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4202

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

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