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You searched for subject:(Molecular Regulation). Showing records 1 – 30 of 590 total matches.

[1] [2] [3] [4] [5] … [20]

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The Ohio State University

1. Hu, Rong. Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2007, The Ohio State University

 The microphthalmia-associated transcription factor (MITF), a basic helix-loop-helix leucine zipper (bHLH-Zip) transcription factor, regulates distinct target genes in several cell types including osteoclasts. Osteoclasts are… (more)

Subjects/Keywords: Biology, Molecular; Cell differentiation; osteoclasts; transcriptional regulation

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APA (6th Edition):

Hu, R. (2007). Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761

Chicago Manual of Style (16th Edition):

Hu, Rong. “Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS.” 2007. Doctoral Dissertation, The Ohio State University. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761.

MLA Handbook (7th Edition):

Hu, Rong. “Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS.” 2007. Web. 22 Oct 2019.

Vancouver:

Hu R. Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761.

Council of Science Editors:

Hu R. Regulation of osteoclast differentiation by transcription factors MITF, PU.1 and EOS. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1166644761


Columbia University

2. Chen, Yaqiong. Studies on RNA Regulation: From Enhancer RNAs to RBBP6 Isoform3.

Degree: 2019, Columbia University

 This dissertation contains two separate yet interconnected pieces of work, which shed light on the complicated RNA regulatory mechanism. The first part, as the main… (more)

Subjects/Keywords: Molecular biology; RNA; Genetic regulation; Biology

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APA (6th Edition):

Chen, Y. (2019). Studies on RNA Regulation: From Enhancer RNAs to RBBP6 Isoform3. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-e3p7-st32

Chicago Manual of Style (16th Edition):

Chen, Yaqiong. “Studies on RNA Regulation: From Enhancer RNAs to RBBP6 Isoform3.” 2019. Doctoral Dissertation, Columbia University. Accessed October 22, 2019. https://doi.org/10.7916/d8-e3p7-st32.

MLA Handbook (7th Edition):

Chen, Yaqiong. “Studies on RNA Regulation: From Enhancer RNAs to RBBP6 Isoform3.” 2019. Web. 22 Oct 2019.

Vancouver:

Chen Y. Studies on RNA Regulation: From Enhancer RNAs to RBBP6 Isoform3. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2019 Oct 22]. Available from: https://doi.org/10.7916/d8-e3p7-st32.

Council of Science Editors:

Chen Y. Studies on RNA Regulation: From Enhancer RNAs to RBBP6 Isoform3. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-e3p7-st32


University of California – Riverside

3. Lee, Travis. Genome-Scale Investigation of Integrated Nuclear and Cytoplasmic Gene Regulatory Control in Arabidopsis.

Degree: Plant Biology, 2018, University of California – Riverside

 Plants are resilient to transient limitations in the availability of oxygen for efficient energy production. The highly reversible response to oxygen deprivation (hypoxia) is characterized… (more)

Subjects/Keywords: Molecular biology; Plant sciences; Bioinformatics; Epigenetic regulation; Hypoxia; Transcriptional regulation; Translational regulation

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APA (6th Edition):

Lee, T. (2018). Genome-Scale Investigation of Integrated Nuclear and Cytoplasmic Gene Regulatory Control in Arabidopsis. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/5t76q98p

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):

Lee, Travis. “Genome-Scale Investigation of Integrated Nuclear and Cytoplasmic Gene Regulatory Control in Arabidopsis.” 2018. Thesis, University of California – Riverside. Accessed October 22, 2019. http://www.escholarship.org/uc/item/5t76q98p.

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

MLA Handbook (7th Edition):

Lee, Travis. “Genome-Scale Investigation of Integrated Nuclear and Cytoplasmic Gene Regulatory Control in Arabidopsis.” 2018. Web. 22 Oct 2019.

Vancouver:

Lee T. Genome-Scale Investigation of Integrated Nuclear and Cytoplasmic Gene Regulatory Control in Arabidopsis. [Internet] [Thesis]. University of California – Riverside; 2018. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/5t76q98p.

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

Council of Science Editors:

Lee T. Genome-Scale Investigation of Integrated Nuclear and Cytoplasmic Gene Regulatory Control in Arabidopsis. [Thesis]. University of California – Riverside; 2018. Available from: http://www.escholarship.org/uc/item/5t76q98p

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


University of Washington

4. Knouf, Emily. The regulation of microRNAs in cancer through novel transcriptional and post-transcriptional mechanisms.

Degree: PhD, 2013, University of Washington

 MicroRNAs are small non-coding RNA molecules that serve as important regulators of gene expression. While understanding of the functional roles of miRNAs in both normal… (more)

Subjects/Keywords: Cancer; MicroRNA; Regulation; Molecular biology; molecular and cellular biology

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APA (6th Edition):

Knouf, E. (2013). The regulation of microRNAs in cancer through novel transcriptional and post-transcriptional mechanisms. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/22582

Chicago Manual of Style (16th Edition):

Knouf, Emily. “The regulation of microRNAs in cancer through novel transcriptional and post-transcriptional mechanisms.” 2013. Doctoral Dissertation, University of Washington. Accessed October 22, 2019. http://hdl.handle.net/1773/22582.

MLA Handbook (7th Edition):

Knouf, Emily. “The regulation of microRNAs in cancer through novel transcriptional and post-transcriptional mechanisms.” 2013. Web. 22 Oct 2019.

Vancouver:

Knouf E. The regulation of microRNAs in cancer through novel transcriptional and post-transcriptional mechanisms. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1773/22582.

Council of Science Editors:

Knouf E. The regulation of microRNAs in cancer through novel transcriptional and post-transcriptional mechanisms. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/22582


Temple University

5. Zumbrun, Steven David. Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b.

Degree: PhD, 2008, Temple University

Molecular Biology and Genetics

The GADD45 family of proteins consists of three small nuclear proteins, GADD45A, GADD45B, and GADD45G, which are implicated in modulating the… (more)

Subjects/Keywords: Biology, Molecular; gadd45b; MMS; post-transcriptional regulation; Sorbitol; stress response; transcriptional regulation

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APA (6th Edition):

Zumbrun, S. D. (2008). Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,23355

Chicago Manual of Style (16th Edition):

Zumbrun, Steven David. “Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b.” 2008. Doctoral Dissertation, Temple University. Accessed October 22, 2019. http://digital.library.temple.edu/u?/p245801coll10,23355.

MLA Handbook (7th Edition):

Zumbrun, Steven David. “Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b.” 2008. Web. 22 Oct 2019.

Vancouver:

Zumbrun SD. Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b. [Internet] [Doctoral dissertation]. Temple University; 2008. [cited 2019 Oct 22]. Available from: http://digital.library.temple.edu/u?/p245801coll10,23355.

Council of Science Editors:

Zumbrun SD. Distinct Mechanisms Regulate Induction of Stress Effector, gadd45b. [Doctoral Dissertation]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,23355


UCLA

6. Sewell, Jared Allan. The Molecular Mechanisms Governing Shoot Stem Cell Maintenance and Organ Patterning by a Family of Transcription Factors in Arabidopsis thaliana.

Degree: Molec, Cell, & Dev Biology, 2016, UCLA

 Genome duplication in eukaryotes and particularly in plant species has led to gene families with both redundant and specialized functions. How closely related transcription factor… (more)

Subjects/Keywords: Molecular biology; Developmental biology; Genetics; Arabidopsis; Gene regulation; homeodomain; Stem cells; Transcriptional regulation; Transcription factors

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APA (6th Edition):

Sewell, J. A. (2016). The Molecular Mechanisms Governing Shoot Stem Cell Maintenance and Organ Patterning by a Family of Transcription Factors in Arabidopsis thaliana. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1673p683

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):

Sewell, Jared Allan. “The Molecular Mechanisms Governing Shoot Stem Cell Maintenance and Organ Patterning by a Family of Transcription Factors in Arabidopsis thaliana.” 2016. Thesis, UCLA. Accessed October 22, 2019. http://www.escholarship.org/uc/item/1673p683.

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

MLA Handbook (7th Edition):

Sewell, Jared Allan. “The Molecular Mechanisms Governing Shoot Stem Cell Maintenance and Organ Patterning by a Family of Transcription Factors in Arabidopsis thaliana.” 2016. Web. 22 Oct 2019.

Vancouver:

Sewell JA. The Molecular Mechanisms Governing Shoot Stem Cell Maintenance and Organ Patterning by a Family of Transcription Factors in Arabidopsis thaliana. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/1673p683.

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

Council of Science Editors:

Sewell JA. The Molecular Mechanisms Governing Shoot Stem Cell Maintenance and Organ Patterning by a Family of Transcription Factors in Arabidopsis thaliana. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/1673p683

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


University of California – Riverside

7. Rodriguez, Kevin Wilfredo. WUSCHEL Mediated Bifunctional Transcriptional Regulation of CLAVATA3 Levels and Spatial Pattern in Arabidopsis thaliana.

Degree: Cell, Molecular and Developmental Biology, 2017, University of California – Riverside

 The balance between self-renewing stem cell divisions and differentiation of stem cell progeny in Shoot Apical Meristems (SAMs) is crucial for the development of all… (more)

Subjects/Keywords: Biology; Developmental biology; Molecular biology; CLAVATA3; ENHANCERS; REGULATION; TRANSCRIPTIONAL REGULATION; TRANSCRIPTION FACTOR; WUSCHEL

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APA (6th Edition):

Rodriguez, K. W. (2017). WUSCHEL Mediated Bifunctional Transcriptional Regulation of CLAVATA3 Levels and Spatial Pattern in Arabidopsis thaliana. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/61h2x729

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):

Rodriguez, Kevin Wilfredo. “WUSCHEL Mediated Bifunctional Transcriptional Regulation of CLAVATA3 Levels and Spatial Pattern in Arabidopsis thaliana.” 2017. Thesis, University of California – Riverside. Accessed October 22, 2019. http://www.escholarship.org/uc/item/61h2x729.

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

MLA Handbook (7th Edition):

Rodriguez, Kevin Wilfredo. “WUSCHEL Mediated Bifunctional Transcriptional Regulation of CLAVATA3 Levels and Spatial Pattern in Arabidopsis thaliana.” 2017. Web. 22 Oct 2019.

Vancouver:

Rodriguez KW. WUSCHEL Mediated Bifunctional Transcriptional Regulation of CLAVATA3 Levels and Spatial Pattern in Arabidopsis thaliana. [Internet] [Thesis]. University of California – Riverside; 2017. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/61h2x729.

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

Council of Science Editors:

Rodriguez KW. WUSCHEL Mediated Bifunctional Transcriptional Regulation of CLAVATA3 Levels and Spatial Pattern in Arabidopsis thaliana. [Thesis]. University of California – Riverside; 2017. Available from: http://www.escholarship.org/uc/item/61h2x729

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


UCLA

8. Liu, Xin Liu. The Selective and Combinatorial Regulation of Toll-Like Receptor-Activated Transcriptional Cascades.

Degree: Molecular Biology, 2017, UCLA

 The immune system is essential for host defense to pathogen infection, tissue repair, stress response, and other physiological functions. An unbalanced immune system is detrimental… (more)

Subjects/Keywords: Molecular biology; Gene regulation; Innate immunity; Selective regulation; Serum response factor; Toll-like receptor

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APA (6th Edition):

Liu, X. L. (2017). The Selective and Combinatorial Regulation of Toll-Like Receptor-Activated Transcriptional Cascades. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/7k44j89n

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):

Liu, Xin Liu. “The Selective and Combinatorial Regulation of Toll-Like Receptor-Activated Transcriptional Cascades.” 2017. Thesis, UCLA. Accessed October 22, 2019. http://www.escholarship.org/uc/item/7k44j89n.

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

MLA Handbook (7th Edition):

Liu, Xin Liu. “The Selective and Combinatorial Regulation of Toll-Like Receptor-Activated Transcriptional Cascades.” 2017. Web. 22 Oct 2019.

Vancouver:

Liu XL. The Selective and Combinatorial Regulation of Toll-Like Receptor-Activated Transcriptional Cascades. [Internet] [Thesis]. UCLA; 2017. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/7k44j89n.

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

Council of Science Editors:

Liu XL. The Selective and Combinatorial Regulation of Toll-Like Receptor-Activated Transcriptional Cascades. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/7k44j89n

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


University of California – San Francisco

9. Schiller, Benjamin Joseph. Data Biology: A quantitative exploration of gene regulation and underlying mechanisms.

Degree: Biochemistry and Molecular Biology, 2013, University of California – San Francisco

Regulation of gene expression is a fundamental biological process required to adapt the full set of hereditary information (i.e., the genome) to the varied environments… (more)

Subjects/Keywords: Molecular biology; Bioinformatics; Biochemistry; gene regulation; glucocorticoid receptor; glucocorticoid response element; GR; motif; transcriptional regulation

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APA (6th Edition):

Schiller, B. J. (2013). Data Biology: A quantitative exploration of gene regulation and underlying mechanisms. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2rc2q811

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):

Schiller, Benjamin Joseph. “Data Biology: A quantitative exploration of gene regulation and underlying mechanisms.” 2013. Thesis, University of California – San Francisco. Accessed October 22, 2019. http://www.escholarship.org/uc/item/2rc2q811.

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

MLA Handbook (7th Edition):

Schiller, Benjamin Joseph. “Data Biology: A quantitative exploration of gene regulation and underlying mechanisms.” 2013. Web. 22 Oct 2019.

Vancouver:

Schiller BJ. Data Biology: A quantitative exploration of gene regulation and underlying mechanisms. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/2rc2q811.

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

Council of Science Editors:

Schiller BJ. Data Biology: A quantitative exploration of gene regulation and underlying mechanisms. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/2rc2q811

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


University of California – San Francisco

10. Chen, Amy Fan. Epigenetic regulation of the transition from naïve to formative pluripotency.

Degree: Biomedical Sciences, 2017, University of California – San Francisco

 Many epigenetic changes occur around implantation as pluripotent cells of the epiblast prepare for lineage specification. However, in vivo epigenetic studies during these early developmental… (more)

Subjects/Keywords: Molecular biology; Developmental biology; enhancer regulation; epigenetics; gene regulation; pluripotency; stem cells

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APA (6th Edition):

Chen, A. F. (2017). Epigenetic regulation of the transition from naïve to formative pluripotency. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0512c0nq

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):

Chen, Amy Fan. “Epigenetic regulation of the transition from naïve to formative pluripotency.” 2017. Thesis, University of California – San Francisco. Accessed October 22, 2019. http://www.escholarship.org/uc/item/0512c0nq.

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

MLA Handbook (7th Edition):

Chen, Amy Fan. “Epigenetic regulation of the transition from naïve to formative pluripotency.” 2017. Web. 22 Oct 2019.

Vancouver:

Chen AF. Epigenetic regulation of the transition from naïve to formative pluripotency. [Internet] [Thesis]. University of California – San Francisco; 2017. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/0512c0nq.

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

Council of Science Editors:

Chen AF. Epigenetic regulation of the transition from naïve to formative pluripotency. [Thesis]. University of California – San Francisco; 2017. Available from: http://www.escholarship.org/uc/item/0512c0nq

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


University of Pennsylvania

11. Venters, Christopher. U1 Snrnp Telescripting: A Transcriptional Regulation Mechanism That Has Driven Intron Size Expansion Across Evolution.

Degree: 2019, University of Pennsylvania

 U1 snRNP (U1) functions in controlling transcription through both the splicing of introns and the suppression of premature cleavage and polyadenylation. The latter, termed telescripting,… (more)

Subjects/Keywords: Evolution; Genome structure; Splicing regulation; Telescripting; Transcription regulation; U1 snRNP; Bioinformatics; Cell Biology; Molecular Biology

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APA (6th Edition):

Venters, C. (2019). U1 Snrnp Telescripting: A Transcriptional Regulation Mechanism That Has Driven Intron Size Expansion Across Evolution. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3240

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):

Venters, Christopher. “U1 Snrnp Telescripting: A Transcriptional Regulation Mechanism That Has Driven Intron Size Expansion Across Evolution.” 2019. Thesis, University of Pennsylvania. Accessed October 22, 2019. https://repository.upenn.edu/edissertations/3240.

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

MLA Handbook (7th Edition):

Venters, Christopher. “U1 Snrnp Telescripting: A Transcriptional Regulation Mechanism That Has Driven Intron Size Expansion Across Evolution.” 2019. Web. 22 Oct 2019.

Vancouver:

Venters C. U1 Snrnp Telescripting: A Transcriptional Regulation Mechanism That Has Driven Intron Size Expansion Across Evolution. [Internet] [Thesis]. University of Pennsylvania; 2019. [cited 2019 Oct 22]. Available from: https://repository.upenn.edu/edissertations/3240.

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

Council of Science Editors:

Venters C. U1 Snrnp Telescripting: A Transcriptional Regulation Mechanism That Has Driven Intron Size Expansion Across Evolution. [Thesis]. University of Pennsylvania; 2019. Available from: https://repository.upenn.edu/edissertations/3240

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


University of Lethbridge

12. University of Lethbridge. Faculty of Arts and Science. Allosteric regulation and function of GTPases .

Degree: 2019, University of Lethbridge

 Guanosine triphosphatases (GTPases) are some of the most vital and versatile molecular switches found in all domains of life. For proper functionality these enzymes require… (more)

Subjects/Keywords: Guanosine triphosphatase  – Research; Allosteric regulation  – Research; Enzymes  – Regulation  – Research; allosteric regulation; allostery; EF-Tu; GTPases; guanosine triphosphatases; molecular switches; Dissertations, Academic

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APA (6th Edition):

Science, U. o. L. F. o. A. a. (2019). Allosteric regulation and function of GTPases . (Thesis). University of Lethbridge. Retrieved from http://hdl.handle.net/10133/5493

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):

Science, University of Lethbridge. Faculty of Arts and. “Allosteric regulation and function of GTPases .” 2019. Thesis, University of Lethbridge. Accessed October 22, 2019. http://hdl.handle.net/10133/5493.

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

MLA Handbook (7th Edition):

Science, University of Lethbridge. Faculty of Arts and. “Allosteric regulation and function of GTPases .” 2019. Web. 22 Oct 2019.

Vancouver:

Science UoLFoAa. Allosteric regulation and function of GTPases . [Internet] [Thesis]. University of Lethbridge; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10133/5493.

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

Council of Science Editors:

Science UoLFoAa. Allosteric regulation and function of GTPases . [Thesis]. University of Lethbridge; 2019. Available from: http://hdl.handle.net/10133/5493

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


East Carolina University

13. Henderson, Laura M. Psf2, a member of the heterotetrameric GINS Complex, plays a role in cell cycle progression and maintenance of genomic integrity.

Degree: 2010, East Carolina University

 Multiple proteins are involved in the complete and accurate replication of the genome during S phase of the cell cycle. At the G1/S phase transition,… (more)

Subjects/Keywords: Biology, Molecular; Biology, Cell; Cell Biology; Molecular biology; Genomics; Genomes; Proteins; DNA replication – Regulation; Cell cycle – Regulation; Eukaryotic cells

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APA (6th Edition):

Henderson, L. M. (2010). Psf2, a member of the heterotetrameric GINS Complex, plays a role in cell cycle progression and maintenance of genomic integrity. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/2877

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):

Henderson, Laura M. “Psf2, a member of the heterotetrameric GINS Complex, plays a role in cell cycle progression and maintenance of genomic integrity.” 2010. Thesis, East Carolina University. Accessed October 22, 2019. http://hdl.handle.net/10342/2877.

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

MLA Handbook (7th Edition):

Henderson, Laura M. “Psf2, a member of the heterotetrameric GINS Complex, plays a role in cell cycle progression and maintenance of genomic integrity.” 2010. Web. 22 Oct 2019.

Vancouver:

Henderson LM. Psf2, a member of the heterotetrameric GINS Complex, plays a role in cell cycle progression and maintenance of genomic integrity. [Internet] [Thesis]. East Carolina University; 2010. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10342/2877.

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

Council of Science Editors:

Henderson LM. Psf2, a member of the heterotetrameric GINS Complex, plays a role in cell cycle progression and maintenance of genomic integrity. [Thesis]. East Carolina University; 2010. Available from: http://hdl.handle.net/10342/2877

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


Temple University

14. Korostowski, Lisa. Transcript Regulation within the Kcnq1 Domain.

Degree: PhD, 2012, Temple University

Molecular Biology and Genetics

Epigenetics was a term first coined to understand how cells with the same genetic make up can differentiate into various cell… (more)

Subjects/Keywords: Molecular biology; Genetics;

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APA (6th Edition):

Korostowski, L. (2012). Transcript Regulation within the Kcnq1 Domain. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,235191

Chicago Manual of Style (16th Edition):

Korostowski, Lisa. “Transcript Regulation within the Kcnq1 Domain.” 2012. Doctoral Dissertation, Temple University. Accessed October 22, 2019. http://digital.library.temple.edu/u?/p245801coll10,235191.

MLA Handbook (7th Edition):

Korostowski, Lisa. “Transcript Regulation within the Kcnq1 Domain.” 2012. Web. 22 Oct 2019.

Vancouver:

Korostowski L. Transcript Regulation within the Kcnq1 Domain. [Internet] [Doctoral dissertation]. Temple University; 2012. [cited 2019 Oct 22]. Available from: http://digital.library.temple.edu/u?/p245801coll10,235191.

Council of Science Editors:

Korostowski L. Transcript Regulation within the Kcnq1 Domain. [Doctoral Dissertation]. Temple University; 2012. Available from: http://digital.library.temple.edu/u?/p245801coll10,235191


East Carolina University

15. Robins, Joshua Eli. SPATIAL EXPRESSION OF MATRIX AND MATRIX RECEPTOR PROTEINS IN THE DEVELOPING SYNOVIAL JOINT.

Degree: 2013, East Carolina University

 Little is understood about the complex spatial and temporal molecular interactions necessary to form a fully functional synovial joint. Understanding molecular pathways and signaling within… (more)

Subjects/Keywords: Biology; Developmental biology; Molecular biology; Biology, Molecular; Gene expression; Genetic regulation; Joints; Embryology

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APA (6th Edition):

Robins, J. E. (2013). SPATIAL EXPRESSION OF MATRIX AND MATRIX RECEPTOR PROTEINS IN THE DEVELOPING SYNOVIAL JOINT. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4194

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):

Robins, Joshua Eli. “SPATIAL EXPRESSION OF MATRIX AND MATRIX RECEPTOR PROTEINS IN THE DEVELOPING SYNOVIAL JOINT.” 2013. Thesis, East Carolina University. Accessed October 22, 2019. http://hdl.handle.net/10342/4194.

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

MLA Handbook (7th Edition):

Robins, Joshua Eli. “SPATIAL EXPRESSION OF MATRIX AND MATRIX RECEPTOR PROTEINS IN THE DEVELOPING SYNOVIAL JOINT.” 2013. Web. 22 Oct 2019.

Vancouver:

Robins JE. SPATIAL EXPRESSION OF MATRIX AND MATRIX RECEPTOR PROTEINS IN THE DEVELOPING SYNOVIAL JOINT. [Internet] [Thesis]. East Carolina University; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10342/4194.

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

Council of Science Editors:

Robins JE. SPATIAL EXPRESSION OF MATRIX AND MATRIX RECEPTOR PROTEINS IN THE DEVELOPING SYNOVIAL JOINT. [Thesis]. East Carolina University; 2013. Available from: http://hdl.handle.net/10342/4194

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


East Carolina University

16. Rummings, Wayne Anthony, Jr. Investigating the Interaction of RecQL4 and Mcm10 in Drosophila melanogaster.

Degree: 2014, East Carolina University

 Accurate duplication and regulation of the eukaryotic genome requires precise coordination among multiple replication factors. RecQL4, the least characterized RecQ protein, is a 1208 amino… (more)

Subjects/Keywords: Biology, Molecular; Molecular biology; Drosophila melanogaster; Eukaryotic cells – Genetics; Genetic regulation; Amino acids; Mutation (Biology)

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APA (6th Edition):

Rummings, Wayne Anthony, J. (2014). Investigating the Interaction of RecQL4 and Mcm10 in Drosophila melanogaster. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4551

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):

Rummings, Wayne Anthony, Jr. “Investigating the Interaction of RecQL4 and Mcm10 in Drosophila melanogaster.” 2014. Thesis, East Carolina University. Accessed October 22, 2019. http://hdl.handle.net/10342/4551.

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

MLA Handbook (7th Edition):

Rummings, Wayne Anthony, Jr. “Investigating the Interaction of RecQL4 and Mcm10 in Drosophila melanogaster.” 2014. Web. 22 Oct 2019.

Vancouver:

Rummings, Wayne Anthony J. Investigating the Interaction of RecQL4 and Mcm10 in Drosophila melanogaster. [Internet] [Thesis]. East Carolina University; 2014. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/10342/4551.

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

Council of Science Editors:

Rummings, Wayne Anthony J. Investigating the Interaction of RecQL4 and Mcm10 in Drosophila melanogaster. [Thesis]. East Carolina University; 2014. Available from: http://hdl.handle.net/10342/4551

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


UCLA

17. Jacobitz, Alex William. The Molecular Basis of Substrate Recognition, Catalysis, and Regulation in Sortase Enzymes.

Degree: Biochemistry & Molecular Biology, 2015, UCLA

 The Molecular Basis of Substrate Recognition, Catalysis, and Regulation in Sortase EnzymesByAlex William JacobitzDoctor of Philosophy in Biochemistry and Molecular Biology University of California, Los… (more)

Subjects/Keywords: Biochemistry; Biophysics; Molecular biology; Crystallography; Enzyme Regulation; Molecular Dynamics; NMR; Protein Structure; Sortase

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APA (6th Edition):

Jacobitz, A. W. (2015). The Molecular Basis of Substrate Recognition, Catalysis, and Regulation in Sortase Enzymes. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/625123dg

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):

Jacobitz, Alex William. “The Molecular Basis of Substrate Recognition, Catalysis, and Regulation in Sortase Enzymes.” 2015. Thesis, UCLA. Accessed October 22, 2019. http://www.escholarship.org/uc/item/625123dg.

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

MLA Handbook (7th Edition):

Jacobitz, Alex William. “The Molecular Basis of Substrate Recognition, Catalysis, and Regulation in Sortase Enzymes.” 2015. Web. 22 Oct 2019.

Vancouver:

Jacobitz AW. The Molecular Basis of Substrate Recognition, Catalysis, and Regulation in Sortase Enzymes. [Internet] [Thesis]. UCLA; 2015. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/625123dg.

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

Council of Science Editors:

Jacobitz AW. The Molecular Basis of Substrate Recognition, Catalysis, and Regulation in Sortase Enzymes. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/625123dg

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

18. Patwardhan, Rupali P. Massively parallel functional dissection of regulatory elements.

Degree: PhD, 2013, University of Washington

 Massively parallel sequencing has accelerated the cataloging of cis-regulatory elements in mammalian genomes. However, it remains challenging to estimate the functional effects of variation in… (more)

Subjects/Keywords: functional genomics; genomics; massively parallel; molecular tagging; regulation; regulatory elements; Genetics; Molecular biology; Genetics

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APA (6th Edition):

Patwardhan, R. P. (2013). Massively parallel functional dissection of regulatory elements. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/21833

Chicago Manual of Style (16th Edition):

Patwardhan, Rupali P. “Massively parallel functional dissection of regulatory elements.” 2013. Doctoral Dissertation, University of Washington. Accessed October 22, 2019. http://hdl.handle.net/1773/21833.

MLA Handbook (7th Edition):

Patwardhan, Rupali P. “Massively parallel functional dissection of regulatory elements.” 2013. Web. 22 Oct 2019.

Vancouver:

Patwardhan RP. Massively parallel functional dissection of regulatory elements. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1773/21833.

Council of Science Editors:

Patwardhan RP. Massively parallel functional dissection of regulatory elements. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/21833


University of California – San Francisco

19. Sorrells, Trevor Rick. Constraint and Facilitation in the Evolution of Transcription Networks.

Degree: Biochemistry and Molecular Biology, 2016, University of California – San Francisco

 The mystery of how diverse life forms evolved has captivated scientists for over 150 years. It has become clear that many diverse life forms harbor… (more)

Subjects/Keywords: Molecular biology; Evolution & development; Bioinformatics; Epistasis; Genetics; Molecular evolution; Network biology; Systems biology; Transcription regulation

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APA (6th Edition):

Sorrells, T. R. (2016). Constraint and Facilitation in the Evolution of Transcription Networks. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/6fj6n5cs

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):

Sorrells, Trevor Rick. “Constraint and Facilitation in the Evolution of Transcription Networks.” 2016. Thesis, University of California – San Francisco. Accessed October 22, 2019. http://www.escholarship.org/uc/item/6fj6n5cs.

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

MLA Handbook (7th Edition):

Sorrells, Trevor Rick. “Constraint and Facilitation in the Evolution of Transcription Networks.” 2016. Web. 22 Oct 2019.

Vancouver:

Sorrells TR. Constraint and Facilitation in the Evolution of Transcription Networks. [Internet] [Thesis]. University of California – San Francisco; 2016. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/6fj6n5cs.

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

Council of Science Editors:

Sorrells TR. Constraint and Facilitation in the Evolution of Transcription Networks. [Thesis]. University of California – San Francisco; 2016. Available from: http://www.escholarship.org/uc/item/6fj6n5cs

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


University of Washington

20. Cai, Yi. Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance.

Degree: PhD, 2019, University of Washington

 Morphologically and functionally normal human skin carries a surprisingly high burden of oncogenic lesions, suggesting that the skin has exceptional capacity to tolerate oncogene hyperactivity.… (more)

Subjects/Keywords: Cancer; Disease model; Stem cell regulation; Molecular biology; Biology; Cellular biology; Molecular and cellular biology

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APA (6th Edition):

Cai, Y. (2019). Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/44393

Chicago Manual of Style (16th Edition):

Cai, Yi. “Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance.” 2019. Doctoral Dissertation, University of Washington. Accessed October 22, 2019. http://hdl.handle.net/1773/44393.

MLA Handbook (7th Edition):

Cai, Yi. “Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance.” 2019. Web. 22 Oct 2019.

Vancouver:

Cai Y. Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1773/44393.

Council of Science Editors:

Cai Y. Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/44393


Temple University

21. Barton, Maria. Lnc-EPCAM AND Lnc-BHLHE41 AS RNA REGULATORS OF BREAST CANCER AND BREAST CANCER PREVENTION.

Degree: PhD, 2017, Temple University

Biochemistry

The objective of this study was to unveil a novel area of gene regulation in breast cancer and breast cancer prevention through the study… (more)

Subjects/Keywords: Cellular biology; Molecular biology; Biochemistry;

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APA (6th Edition):

Barton, M. (2017). Lnc-EPCAM AND Lnc-BHLHE41 AS RNA REGULATORS OF BREAST CANCER AND BREAST CANCER PREVENTION. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,424232

Chicago Manual of Style (16th Edition):

Barton, Maria. “Lnc-EPCAM AND Lnc-BHLHE41 AS RNA REGULATORS OF BREAST CANCER AND BREAST CANCER PREVENTION.” 2017. Doctoral Dissertation, Temple University. Accessed October 22, 2019. http://digital.library.temple.edu/u?/p245801coll10,424232.

MLA Handbook (7th Edition):

Barton, Maria. “Lnc-EPCAM AND Lnc-BHLHE41 AS RNA REGULATORS OF BREAST CANCER AND BREAST CANCER PREVENTION.” 2017. Web. 22 Oct 2019.

Vancouver:

Barton M. Lnc-EPCAM AND Lnc-BHLHE41 AS RNA REGULATORS OF BREAST CANCER AND BREAST CANCER PREVENTION. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2019 Oct 22]. Available from: http://digital.library.temple.edu/u?/p245801coll10,424232.

Council of Science Editors:

Barton M. Lnc-EPCAM AND Lnc-BHLHE41 AS RNA REGULATORS OF BREAST CANCER AND BREAST CANCER PREVENTION. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,424232


The Ohio State University

22. Li, Jing. Biological function of E2F7 and E2F8 is essential for embryo development.

Degree: PhD, Molecular Genetics, 2009, The Ohio State University

  The novel E2F7 and E2F8 family members are thought to function as transcriptional repressors important for the control of cell proliferation in vitro. However,… (more)

Subjects/Keywords: Genetics; Molecular Biology; E2F; embryo development; apoptosis; cell cycle; transcriptional regulation

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APA (6th Edition):

Li, J. (2009). Biological function of E2F7 and E2F8 is essential for embryo development. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018

Chicago Manual of Style (16th Edition):

Li, Jing. “Biological function of E2F7 and E2F8 is essential for embryo development.” 2009. Doctoral Dissertation, The Ohio State University. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018.

MLA Handbook (7th Edition):

Li, Jing. “Biological function of E2F7 and E2F8 is essential for embryo development.” 2009. Web. 22 Oct 2019.

Vancouver:

Li J. Biological function of E2F7 and E2F8 is essential for embryo development. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018.

Council of Science Editors:

Li J. Biological function of E2F7 and E2F8 is essential for embryo development. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1243873018


Miami University

23. Ghosh, Sushmita. A Molecular, Evolutionary and Functional Study of RNP-4F Splicing Assembly Factor Gene Expression in <i>Drosophila melanogaster</i>.

Degree: PhD, Cell, Molecular and Structural Biology (CMSB), 2016, Miami University

 In the first chapter I have discussed the advantages of <i>Drosophila</i> as a model organism, the FC31 transgenesis system, various aspects of splicing and splice… (more)

Subjects/Keywords: Biology; Molecular Biology; RNP-4F, dADAR, alternative splicing, gene expression regulation

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APA (6th Edition):

Ghosh, S. (2016). A Molecular, Evolutionary and Functional Study of RNP-4F Splicing Assembly Factor Gene Expression in <i>Drosophila melanogaster</i>. (Doctoral Dissertation). Miami University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=miami1465473655

Chicago Manual of Style (16th Edition):

Ghosh, Sushmita. “A Molecular, Evolutionary and Functional Study of RNP-4F Splicing Assembly Factor Gene Expression in <i>Drosophila melanogaster</i>.” 2016. Doctoral Dissertation, Miami University. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=miami1465473655.

MLA Handbook (7th Edition):

Ghosh, Sushmita. “A Molecular, Evolutionary and Functional Study of RNP-4F Splicing Assembly Factor Gene Expression in <i>Drosophila melanogaster</i>.” 2016. Web. 22 Oct 2019.

Vancouver:

Ghosh S. A Molecular, Evolutionary and Functional Study of RNP-4F Splicing Assembly Factor Gene Expression in <i>Drosophila melanogaster</i>. [Internet] [Doctoral dissertation]. Miami University; 2016. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1465473655.

Council of Science Editors:

Ghosh S. A Molecular, Evolutionary and Functional Study of RNP-4F Splicing Assembly Factor Gene Expression in <i>Drosophila melanogaster</i>. [Doctoral Dissertation]. Miami University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=miami1465473655

24. Bennett, Jonathon D. Enhancer Induced Changes In Chromatin Structure And Function.

Degree: 2014, Johns Hopkins University

 Abstract Gene regulation in mammals is a cornerstone issue in developmental biology. One example of gene regulatory elements are enhancers, which have been shown in… (more)

Subjects/Keywords: Molecular Biology; Immunology; Gene Regulation; DNase I Hypersensitivity;

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APA (6th Edition):

Bennett, J. D. (2014). Enhancer Induced Changes In Chromatin Structure And Function. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37163

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):

Bennett, Jonathon D. “Enhancer Induced Changes In Chromatin Structure And Function.” 2014. Thesis, Johns Hopkins University. Accessed October 22, 2019. http://jhir.library.jhu.edu/handle/1774.2/37163.

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

MLA Handbook (7th Edition):

Bennett, Jonathon D. “Enhancer Induced Changes In Chromatin Structure And Function.” 2014. Web. 22 Oct 2019.

Vancouver:

Bennett JD. Enhancer Induced Changes In Chromatin Structure And Function. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2019 Oct 22]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37163.

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

Council of Science Editors:

Bennett JD. Enhancer Induced Changes In Chromatin Structure And Function. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/37163

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


University of Toledo Health Science Campus

25. Mukherjee, Sumanta. LPS induced TH2 (Interleukin-4) cytokine production in macrophages and its regulation.

Degree: PhD, College of Graduate Studies, 2008, University of Toledo Health Science Campus

  Gram negative LPS signaling through TLR4 is a potent inducer of the innate immune system and also directs the adaptive immune response. LPS activation… (more)

Subjects/Keywords: Immunology; Molecular Biology; LPS; macrophage; Th2; cytokine; Il4; regulation

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APA (6th Edition):

Mukherjee, S. (2008). LPS induced TH2 (Interleukin-4) cytokine production in macrophages and its regulation. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1207743729

Chicago Manual of Style (16th Edition):

Mukherjee, Sumanta. “LPS induced TH2 (Interleukin-4) cytokine production in macrophages and its regulation.” 2008. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=mco1207743729.

MLA Handbook (7th Edition):

Mukherjee, Sumanta. “LPS induced TH2 (Interleukin-4) cytokine production in macrophages and its regulation.” 2008. Web. 22 Oct 2019.

Vancouver:

Mukherjee S. LPS induced TH2 (Interleukin-4) cytokine production in macrophages and its regulation. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2008. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1207743729.

Council of Science Editors:

Mukherjee S. LPS induced TH2 (Interleukin-4) cytokine production in macrophages and its regulation. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1207743729


The Ohio State University

26. Tangeman, Larissa J. Regulation of BLM Nucleolar Localization.

Degree: MS, Biomedical Sciences, 2017, The Ohio State University

 Defects in coordinated ribosomal RNA (rRNA) transcription in the nucleolus cause cellular and organismal growth deficiencies. Bloom’s syndrome, an autosomal recessive human disorder caused by… (more)

Subjects/Keywords: Biochemistry; Molecular Biology; Genetics; Regulation, BLM Nucleolar Localization

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APA (6th Edition):

Tangeman, L. J. (2017). Regulation of BLM Nucleolar Localization. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817

Chicago Manual of Style (16th Edition):

Tangeman, Larissa J. “Regulation of BLM Nucleolar Localization.” 2017. Masters Thesis, The Ohio State University. Accessed October 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817.

MLA Handbook (7th Edition):

Tangeman, Larissa J. “Regulation of BLM Nucleolar Localization.” 2017. Web. 22 Oct 2019.

Vancouver:

Tangeman LJ. Regulation of BLM Nucleolar Localization. [Internet] [Masters thesis]. The Ohio State University; 2017. [cited 2019 Oct 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817.

Council of Science Editors:

Tangeman LJ. Regulation of BLM Nucleolar Localization. [Masters Thesis]. The Ohio State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu148347431702817


University of California – Berkeley

27. Mostovoy, Yulia. Regulation and function of antisense transcription in Saccharomyces yeast.

Degree: Molecular & Cell Biology, 2014, University of California – Berkeley

 Transcription of RNA antisense to protein-coding genes is widespread in genomes from bacteria to human. For most antisense transcription, the methods by which it is… (more)

Subjects/Keywords: Genetics; Molecular biology; antisense RNA; gene regulation; noncoding RNA

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APA (6th Edition):

Mostovoy, Y. (2014). Regulation and function of antisense transcription in Saccharomyces yeast. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6q55h0n6

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):

Mostovoy, Yulia. “Regulation and function of antisense transcription in Saccharomyces yeast.” 2014. Thesis, University of California – Berkeley. Accessed October 22, 2019. http://www.escholarship.org/uc/item/6q55h0n6.

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

MLA Handbook (7th Edition):

Mostovoy, Yulia. “Regulation and function of antisense transcription in Saccharomyces yeast.” 2014. Web. 22 Oct 2019.

Vancouver:

Mostovoy Y. Regulation and function of antisense transcription in Saccharomyces yeast. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2019 Oct 22]. Available from: http://www.escholarship.org/uc/item/6q55h0n6.

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

Council of Science Editors:

Mostovoy Y. Regulation and function of antisense transcription in Saccharomyces yeast. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/6q55h0n6

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

28. Linne, Hannah Louise. Investigating telomerase regulation in human breast cancer cells : a search for telomerase repressor sequences localised to chromosome 3P.

Degree: PhD, 2015, Brunel University

 Cellular immortality is one of the ten hallmarks of human cancer and has been shown to be an essential prerequisite for malignant progression (Hanahan and… (more)

Subjects/Keywords: 616.99; hTERT regulation; Immortalisation; Molecular changes associated with cellular immortalisation

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APA (6th Edition):

Linne, H. L. (2015). Investigating telomerase regulation in human breast cancer cells : a search for telomerase repressor sequences localised to chromosome 3P. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/11620 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675877

Chicago Manual of Style (16th Edition):

Linne, Hannah Louise. “Investigating telomerase regulation in human breast cancer cells : a search for telomerase repressor sequences localised to chromosome 3P.” 2015. Doctoral Dissertation, Brunel University. Accessed October 22, 2019. http://bura.brunel.ac.uk/handle/2438/11620 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675877.

MLA Handbook (7th Edition):

Linne, Hannah Louise. “Investigating telomerase regulation in human breast cancer cells : a search for telomerase repressor sequences localised to chromosome 3P.” 2015. Web. 22 Oct 2019.

Vancouver:

Linne HL. Investigating telomerase regulation in human breast cancer cells : a search for telomerase repressor sequences localised to chromosome 3P. [Internet] [Doctoral dissertation]. Brunel University; 2015. [cited 2019 Oct 22]. Available from: http://bura.brunel.ac.uk/handle/2438/11620 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675877.

Council of Science Editors:

Linne HL. Investigating telomerase regulation in human breast cancer cells : a search for telomerase repressor sequences localised to chromosome 3P. [Doctoral Dissertation]. Brunel University; 2015. Available from: http://bura.brunel.ac.uk/handle/2438/11620 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.675877


University of Washington

29. Silverman, Julie Michelle. Posttranslational regulation and effector specificity of the type VI secretion system.

Degree: PhD, 2013, University of Washington

 Bacteria mediate interactions with their surroundings by exporting a variety of proteins into the extracellular environment. Gram-negative bacteria have evolved at least six dedicated secretory… (more)

Subjects/Keywords: Bacterial interactions; Posttranslational regulation; Secretion systems; Microbiology; Molecular biology; Biochemistry; microbiology

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APA (6th Edition):

Silverman, J. M. (2013). Posttranslational regulation and effector specificity of the type VI secretion system. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/24205

Chicago Manual of Style (16th Edition):

Silverman, Julie Michelle. “Posttranslational regulation and effector specificity of the type VI secretion system.” 2013. Doctoral Dissertation, University of Washington. Accessed October 22, 2019. http://hdl.handle.net/1773/24205.

MLA Handbook (7th Edition):

Silverman, Julie Michelle. “Posttranslational regulation and effector specificity of the type VI secretion system.” 2013. Web. 22 Oct 2019.

Vancouver:

Silverman JM. Posttranslational regulation and effector specificity of the type VI secretion system. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2019 Oct 22]. Available from: http://hdl.handle.net/1773/24205.

Council of Science Editors:

Silverman JM. Posttranslational regulation and effector specificity of the type VI secretion system. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/24205


University of Oxford

30. Smythies, James. Characterising the determinants of hypoxia inducible transcription factors binding to chromatin.

Degree: PhD, 2017, University of Oxford

 Hypoxia regulates many hundreds of genes that play important roles in numerous physiological and pathophysiological processes. The hypoxia inducible transcription factors (HIFs) are central to… (more)

Subjects/Keywords: Transcription factors; Gene regulation; Molecular biology; Transcription; Hypoxia

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APA (6th Edition):

Smythies, J. (2017). Characterising the determinants of hypoxia inducible transcription factors binding to chromatin. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:20fc2f64-a46c-40a0-8e2f-ea0e2d81bd16 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748704

Chicago Manual of Style (16th Edition):

Smythies, James. “Characterising the determinants of hypoxia inducible transcription factors binding to chromatin.” 2017. Doctoral Dissertation, University of Oxford. Accessed October 22, 2019. http://ora.ox.ac.uk/objects/uuid:20fc2f64-a46c-40a0-8e2f-ea0e2d81bd16 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748704.

MLA Handbook (7th Edition):

Smythies, James. “Characterising the determinants of hypoxia inducible transcription factors binding to chromatin.” 2017. Web. 22 Oct 2019.

Vancouver:

Smythies J. Characterising the determinants of hypoxia inducible transcription factors binding to chromatin. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2019 Oct 22]. Available from: http://ora.ox.ac.uk/objects/uuid:20fc2f64-a46c-40a0-8e2f-ea0e2d81bd16 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748704.

Council of Science Editors:

Smythies J. Characterising the determinants of hypoxia inducible transcription factors binding to chromatin. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:20fc2f64-a46c-40a0-8e2f-ea0e2d81bd16 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748704

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