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You searched for subject:(Gene Expression Regulation). Showing records 1 – 30 of 761 total matches.

[1] [2] [3] [4] [5] … [26]

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University of Saskatchewan

1. Narayanan, Karthikeyan. SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE.

Degree: 2014, University of Saskatchewan

 Carotenoids are organic pigments that are mainly found in the chloroplasts and chromoplasts of plants and other photosynthetic organisms. Carotenoid molecules containing oxygen, such as… (more)

Subjects/Keywords: Carotneoids; RBP47; KCS19; Gene expression; Gene regulation

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APA (6th Edition):

Narayanan, K. (2014). SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-06-1601

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):

Narayanan, Karthikeyan. “SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE.” 2014. Thesis, University of Saskatchewan. Accessed March 07, 2021. http://hdl.handle.net/10388/ETD-2014-06-1601.

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

MLA Handbook (7th Edition):

Narayanan, Karthikeyan. “SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE.” 2014. Web. 07 Mar 2021.

Vancouver:

Narayanan K. SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10388/ETD-2014-06-1601.

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

Council of Science Editors:

Narayanan K. SCREENING AND CHARACTERIZATION OF ARABIDOPSIS THALIANA MUTANTS WITH ALTERED CAROTENOID PROFILE. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-06-1601

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

2. Alasoo, Kaur. Regulation of gene expression in macrophage immune response.

Degree: PhD, 2017, University of Cambridge

Gene expression quantitative trait loci (eQTL) mapping studies can provide mechanistic insights into the functions of disease-associated variants. However, many eQTLs are cell type and… (more)

Subjects/Keywords: Gene expression; Gene regulation; Chromatin; Genetics

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APA (6th Edition):

Alasoo, K. (2017). Regulation of gene expression in macrophage immune response. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/263855

Chicago Manual of Style (16th Edition):

Alasoo, Kaur. “Regulation of gene expression in macrophage immune response.” 2017. Doctoral Dissertation, University of Cambridge. Accessed March 07, 2021. https://www.repository.cam.ac.uk/handle/1810/263855.

MLA Handbook (7th Edition):

Alasoo, Kaur. “Regulation of gene expression in macrophage immune response.” 2017. Web. 07 Mar 2021.

Vancouver:

Alasoo K. Regulation of gene expression in macrophage immune response. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2021 Mar 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/263855.

Council of Science Editors:

Alasoo K. Regulation of gene expression in macrophage immune response. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/263855


University of Alberta

3. Gesner, Emily. Structural and Functional Characterization of T.thermophilus CasE.

Degree: PhD, Department of Biochemistry, 2011, University of Alberta

 Powerful mechanisms of genetic interference in both unicellular and multicellular organisms are based on the sequence-directed targeting of DNA or RNA by small effector RNAs.… (more)

Subjects/Keywords: CRISPR, RNA, Prokaryotes, gene expression regulation, endonuclease

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APA (6th Edition):

Gesner, E. (2011). Structural and Functional Characterization of T.thermophilus CasE. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/3b591b15d

Chicago Manual of Style (16th Edition):

Gesner, Emily. “Structural and Functional Characterization of T.thermophilus CasE.” 2011. Doctoral Dissertation, University of Alberta. Accessed March 07, 2021. https://era.library.ualberta.ca/files/3b591b15d.

MLA Handbook (7th Edition):

Gesner, Emily. “Structural and Functional Characterization of T.thermophilus CasE.” 2011. Web. 07 Mar 2021.

Vancouver:

Gesner E. Structural and Functional Characterization of T.thermophilus CasE. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2021 Mar 07]. Available from: https://era.library.ualberta.ca/files/3b591b15d.

Council of Science Editors:

Gesner E. Structural and Functional Characterization of T.thermophilus CasE. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/3b591b15d

4. Attanasio, Catia. Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs).

Degree: 2007, Université de Genève

 The comparative analysis of the human and mouse genomes has resulted in the identification of a large number of evolutionarily conserved sequences. The occurence of… (more)

Subjects/Keywords: gene expression regulation

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APA (6th Edition):

Attanasio, C. (2007). Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs). (Thesis). Université de Genève. Retrieved from http://doc.rero.ch/record/8776

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):

Attanasio, Catia. “Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs).” 2007. Thesis, Université de Genève. Accessed March 07, 2021. http://doc.rero.ch/record/8776.

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

MLA Handbook (7th Edition):

Attanasio, Catia. “Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs).” 2007. Web. 07 Mar 2021.

Vancouver:

Attanasio C. Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs). [Internet] [Thesis]. Université de Genève; 2007. [cited 2021 Mar 07]. Available from: http://doc.rero.ch/record/8776.

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

Council of Science Editors:

Attanasio C. Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs). [Thesis]. Université de Genève; 2007. Available from: http://doc.rero.ch/record/8776

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


University of Melbourne

5. Jansz, Natasha. Mechanistic insights into how the epigenetic regulator Smchd1 interacts with and alters the chromatin.

Degree: 2018, University of Melbourne

 Structural Maintenance of Chromosomes, Hinge Domain containing 1 (Smchd1) is critical for the maintenance of X Chromosome Inactivation (XCI), and transcriptional repression at a subset… (more)

Subjects/Keywords: epigenetics; chromatin; Smchd1; regulation of gene expression

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APA (6th Edition):

Jansz, N. (2018). Mechanistic insights into how the epigenetic regulator Smchd1 interacts with and alters the chromatin. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/198093

Chicago Manual of Style (16th Edition):

Jansz, Natasha. “Mechanistic insights into how the epigenetic regulator Smchd1 interacts with and alters the chromatin.” 2018. Doctoral Dissertation, University of Melbourne. Accessed March 07, 2021. http://hdl.handle.net/11343/198093.

MLA Handbook (7th Edition):

Jansz, Natasha. “Mechanistic insights into how the epigenetic regulator Smchd1 interacts with and alters the chromatin.” 2018. Web. 07 Mar 2021.

Vancouver:

Jansz N. Mechanistic insights into how the epigenetic regulator Smchd1 interacts with and alters the chromatin. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/11343/198093.

Council of Science Editors:

Jansz N. Mechanistic insights into how the epigenetic regulator Smchd1 interacts with and alters the chromatin. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/198093


University of Southern California

6. Zhang, Jing. Isoform quantification and splicing regulation analysis in RNA-seq studies.

Degree: PhD, Electrical Engineering, 2015, University of Southern California

 The rapid advances in high-throughput sequencing technologies provide us an opportunity to dissect transcriptomes with unprecedented resolution. Based on RNA-seq studies, alternative splicing has become… (more)

Subjects/Keywords: RNA-seq; alternative splicing; gene expression regulation

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APA (6th Edition):

Zhang, J. (2015). Isoform quantification and splicing regulation analysis in RNA-seq studies. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3668

Chicago Manual of Style (16th Edition):

Zhang, Jing. “Isoform quantification and splicing regulation analysis in RNA-seq studies.” 2015. Doctoral Dissertation, University of Southern California. Accessed March 07, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3668.

MLA Handbook (7th Edition):

Zhang, Jing. “Isoform quantification and splicing regulation analysis in RNA-seq studies.” 2015. Web. 07 Mar 2021.

Vancouver:

Zhang J. Isoform quantification and splicing regulation analysis in RNA-seq studies. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2021 Mar 07]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3668.

Council of Science Editors:

Zhang J. Isoform quantification and splicing regulation analysis in RNA-seq studies. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343497/rec/3668


Michigan State University

7. Uygun, Sahra. Using transcriptome and data science methods to uncover gene regulatory and functional information.

Degree: 2017, Michigan State University

Thesis Ph. D. Michigan State University. Genetics 2017

Even in the well-studied model organisms, there are still genomic regions with unknown function. These genomic regions… (more)

Subjects/Keywords: Gene expression; Genetic transcription – Regulation; Bioinformatics; Genetics

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APA (6th Edition):

Uygun, S. (2017). Using transcriptome and data science methods to uncover gene regulatory and functional information. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:4560

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):

Uygun, Sahra. “Using transcriptome and data science methods to uncover gene regulatory and functional information.” 2017. Thesis, Michigan State University. Accessed March 07, 2021. http://etd.lib.msu.edu/islandora/object/etd:4560.

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

MLA Handbook (7th Edition):

Uygun, Sahra. “Using transcriptome and data science methods to uncover gene regulatory and functional information.” 2017. Web. 07 Mar 2021.

Vancouver:

Uygun S. Using transcriptome and data science methods to uncover gene regulatory and functional information. [Internet] [Thesis]. Michigan State University; 2017. [cited 2021 Mar 07]. Available from: http://etd.lib.msu.edu/islandora/object/etd:4560.

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

Council of Science Editors:

Uygun S. Using transcriptome and data science methods to uncover gene regulatory and functional information. [Thesis]. Michigan State University; 2017. Available from: http://etd.lib.msu.edu/islandora/object/etd:4560

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


Rutgers University

8. Hammond, Gifty Naa Ayeley, 1981-. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.

Degree: MS, Microbiology and Molecular Genetics, 2014, Rutgers University

Gene transcription is mediated by the enzyme RNA polymerase (RNAP). RNAP is a multi subunit nucleotidyl transferase that polymerizes ribonucleotides at the 3’ end of… (more)

Subjects/Keywords: Gene expression; Genetic regulation; Reverse transcriptase

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APA (6th Edition):

Hammond, Gifty Naa Ayeley, 1. (2014). Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/42394/

Chicago Manual of Style (16th Edition):

Hammond, Gifty Naa Ayeley, 1981-. “Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.” 2014. Masters Thesis, Rutgers University. Accessed March 07, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/42394/.

MLA Handbook (7th Edition):

Hammond, Gifty Naa Ayeley, 1981-. “Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested.” 2014. Web. 07 Mar 2021.

Vancouver:

Hammond, Gifty Naa Ayeley 1. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. [Internet] [Masters thesis]. Rutgers University; 2014. [cited 2021 Mar 07]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42394/.

Council of Science Editors:

Hammond, Gifty Naa Ayeley 1. Defining the nanoRNA regulon and the mechanism by which gene expression is controlled and manifested. [Masters Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/42394/


Massey University

9. Yang, Tian. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.

Degree: MSc, Biochemistry, 2013, Massey University

 Lentiviral vectors, originally derived from human immunodeficiency virus, provide highly efficient viral gene delivery vehicles. Lentiviral vectors often use a constitutive promoter to drive the… (more)

Subjects/Keywords: Lentiviral vectors; Gene therapy; Gene expression; Gene regulation; Tetracycline; Genetic vectors

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APA (6th Edition):

Yang, T. (2013). Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/4319

Chicago Manual of Style (16th Edition):

Yang, Tian. “Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.” 2013. Masters Thesis, Massey University. Accessed March 07, 2021. http://hdl.handle.net/10179/4319.

MLA Handbook (7th Edition):

Yang, Tian. “Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.” 2013. Web. 07 Mar 2021.

Vancouver:

Yang T. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. [Internet] [Masters thesis]. Massey University; 2013. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10179/4319.

Council of Science Editors:

Yang T. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. [Masters Thesis]. Massey University; 2013. Available from: http://hdl.handle.net/10179/4319


Columbia University

10. Lachmann, Alexander. Confounding effects in gene expression and their impact on downstream analysis.

Degree: 2016, Columbia University

 The reconstruction of gene regulatory networks is one of the milestones of computational system biology. We introduce a new implementation of ARACNe (Algorithm for the… (more)

Subjects/Keywords: Genetic regulation; Genetic regulation – Data processing; Gene expression; Gene expression – Data processing; Bioinformatics; Gene regulatory networks; Genetics

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APA (6th Edition):

Lachmann, A. (2016). Confounding effects in gene expression and their impact on downstream analysis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D82J6BRF

Chicago Manual of Style (16th Edition):

Lachmann, Alexander. “Confounding effects in gene expression and their impact on downstream analysis.” 2016. Doctoral Dissertation, Columbia University. Accessed March 07, 2021. https://doi.org/10.7916/D82J6BRF.

MLA Handbook (7th Edition):

Lachmann, Alexander. “Confounding effects in gene expression and their impact on downstream analysis.” 2016. Web. 07 Mar 2021.

Vancouver:

Lachmann A. Confounding effects in gene expression and their impact on downstream analysis. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2021 Mar 07]. Available from: https://doi.org/10.7916/D82J6BRF.

Council of Science Editors:

Lachmann A. Confounding effects in gene expression and their impact on downstream analysis. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D82J6BRF

11. Vineetha, S. “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”.

Degree: 2012, Cochin University of Science and Technology

Microarray data analysis is one of data mining tool which is used to extract meaningful information hidden in biological data. One of the major focuses… (more)

Subjects/Keywords: Gene Expression Dataset; Colorectal Cancer; Colon Carcinogenesis; Gene Regulation

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APA (6th Edition):

Vineetha, S. (2012). “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”. (Thesis). Cochin University of Science and Technology. Retrieved from http://dyuthi.cusat.ac.in/purl/3760

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):

Vineetha, S. ““Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”.” 2012. Thesis, Cochin University of Science and Technology. Accessed March 07, 2021. http://dyuthi.cusat.ac.in/purl/3760.

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

MLA Handbook (7th Edition):

Vineetha, S. ““Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”.” 2012. Web. 07 Mar 2021.

Vancouver:

Vineetha S. “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”. [Internet] [Thesis]. Cochin University of Science and Technology; 2012. [cited 2021 Mar 07]. Available from: http://dyuthi.cusat.ac.in/purl/3760.

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

Council of Science Editors:

Vineetha S. “Reconstruction of Gene Regulatory Network from Expression Profile of Plasma RNA Data of Colorectal Cancer Patients using Soft Computing Techniques”. [Thesis]. Cochin University of Science and Technology; 2012. Available from: http://dyuthi.cusat.ac.in/purl/3760

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


Cornell University

12. Kremling, Karl. Regulators of expression in Zea mays.

Degree: PhD, Plant Breeding, 2018, Cornell University

 To assess the impact of regulatory variation on a genomic scale, a large scale gene expression resource was created from seven tissues profiled using 3’… (more)

Subjects/Keywords: GWAS; eQTL; transcriptome; Genetics; Gene regulation; Gene expression; Agriculture; Plant sciences

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APA (6th Edition):

Kremling, K. (2018). Regulators of expression in Zea mays. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59415

Chicago Manual of Style (16th Edition):

Kremling, Karl. “Regulators of expression in Zea mays.” 2018. Doctoral Dissertation, Cornell University. Accessed March 07, 2021. http://hdl.handle.net/1813/59415.

MLA Handbook (7th Edition):

Kremling, Karl. “Regulators of expression in Zea mays.” 2018. Web. 07 Mar 2021.

Vancouver:

Kremling K. Regulators of expression in Zea mays. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1813/59415.

Council of Science Editors:

Kremling K. Regulators of expression in Zea mays. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59415


University of Saskatchewan

13. Degenhardt, Rory Frank. The Ribosomal Protein L23a Family of Arabidopsis thaliana.

Degree: 2008, University of Saskatchewan

 The 80 S cytoplasmic ribosome is the largest of three populations of ribosomes responsible for protein synthesis in plants. It is comprised of two RNA/protein… (more)

Subjects/Keywords: gene regulation; gene expression

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APA (6th Edition):

Degenhardt, R. F. (2008). The Ribosomal Protein L23a Family of Arabidopsis thaliana. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-07142008-061230

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):

Degenhardt, Rory Frank. “The Ribosomal Protein L23a Family of Arabidopsis thaliana.” 2008. Thesis, University of Saskatchewan. Accessed March 07, 2021. http://hdl.handle.net/10388/etd-07142008-061230.

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

MLA Handbook (7th Edition):

Degenhardt, Rory Frank. “The Ribosomal Protein L23a Family of Arabidopsis thaliana.” 2008. Web. 07 Mar 2021.

Vancouver:

Degenhardt RF. The Ribosomal Protein L23a Family of Arabidopsis thaliana. [Internet] [Thesis]. University of Saskatchewan; 2008. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10388/etd-07142008-061230.

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

Council of Science Editors:

Degenhardt RF. The Ribosomal Protein L23a Family of Arabidopsis thaliana. [Thesis]. University of Saskatchewan; 2008. Available from: http://hdl.handle.net/10388/etd-07142008-061230

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


University of Manitoba

14. Lei, Lei. Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells.

Degree: Physiology and Pathophysiology, 2015, University of Manitoba

 OBJECTIVES: The role of heterogeneous nuclear ribonucleoproteins in controlling hormone production is not well-understood. This study aims to determine the regulatory roles of hnRNP L… (more)

Subjects/Keywords: Endocrine; Hormones; RNA; Splicing; Processing; Gene regulation; Gene expression; Molecular biology

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APA (6th Edition):

Lei, L. (2015). Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30848

Chicago Manual of Style (16th Edition):

Lei, Lei. “Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells.” 2015. Masters Thesis, University of Manitoba. Accessed March 07, 2021. http://hdl.handle.net/1993/30848.

MLA Handbook (7th Edition):

Lei, Lei. “Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells.” 2015. Web. 07 Mar 2021.

Vancouver:

Lei L. Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells. [Internet] [Masters thesis]. University of Manitoba; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1993/30848.

Council of Science Editors:

Lei L. Differential roles of RNA binding proteins hnRNP L and LL in hormone production in rat pituitary cells. [Masters Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/30848


IUPUI

15. Robison, Jennifer Dawn. Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene.

Degree: 2019, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Abiotic stresses, such as cold, are serious agricultural problems resulting in substantial crop and revenue losses. Soybean (Glycine max) is… (more)

Subjects/Keywords: CBF/DREB; Ethylene; Cold stress; Gene expression; Gene regulation; Soybean; Photosynthesis

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APA (6th Edition):

Robison, J. D. (2019). Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/18927

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):

Robison, Jennifer Dawn. “Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene.” 2019. Thesis, IUPUI. Accessed March 07, 2021. http://hdl.handle.net/1805/18927.

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

MLA Handbook (7th Edition):

Robison, Jennifer Dawn. “Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene.” 2019. Web. 07 Mar 2021.

Vancouver:

Robison JD. Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene. [Internet] [Thesis]. IUPUI; 2019. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1805/18927.

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

Council of Science Editors:

Robison JD. Molecular and Physiological Responses of Soybean (Glycine max) to Cold and the Stress Hormone Ethylene. [Thesis]. IUPUI; 2019. Available from: http://hdl.handle.net/1805/18927

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


University of Bristol

16. Bartoli, Vittorio. Tuneable synthetic genetic devices.

Degree: PhD, 2020, University of Bristol

 Synthetic genetic circuits are gene regulatory networks used to engineer biological systems to carry out useful functions. Moving circuits between environments or host cells alters… (more)

Subjects/Keywords: Synthetic Biology; Systems Biology; Gene regulation; Gene expression; Genetic circuit engineering

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

APA (6th Edition):

Bartoli, V. (2020). Tuneable synthetic genetic devices. (Doctoral Dissertation). University of Bristol. Retrieved from http://hdl.handle.net/1983/c3a4a9b8-3a6a-4f6b-9be0-61e2411116f4

Chicago Manual of Style (16th Edition):

Bartoli, Vittorio. “Tuneable synthetic genetic devices.” 2020. Doctoral Dissertation, University of Bristol. Accessed March 07, 2021. http://hdl.handle.net/1983/c3a4a9b8-3a6a-4f6b-9be0-61e2411116f4.

MLA Handbook (7th Edition):

Bartoli, Vittorio. “Tuneable synthetic genetic devices.” 2020. Web. 07 Mar 2021.

Vancouver:

Bartoli V. Tuneable synthetic genetic devices. [Internet] [Doctoral dissertation]. University of Bristol; 2020. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1983/c3a4a9b8-3a6a-4f6b-9be0-61e2411116f4.

Council of Science Editors:

Bartoli V. Tuneable synthetic genetic devices. [Doctoral Dissertation]. University of Bristol; 2020. Available from: http://hdl.handle.net/1983/c3a4a9b8-3a6a-4f6b-9be0-61e2411116f4


New Jersey Institute of Technology

17. Somoza, Maria E. Gene network understanding and analysis.

Degree: MSin Bioinformatics - (M.S.), Computer Science, 2016, New Jersey Institute of Technology

Gene regulatory network (GRN) is a collection of regulators that interact with each other in the cell to govern the gene expression levels of… (more)

Subjects/Keywords: Gene regulatory network; Transcriptional gene regulation; Gene co-expression networks; Correlation networks; Bioinformatics; Computer Sciences

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

APA (6th Edition):

Somoza, M. E. (2016). Gene network understanding and analysis. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/279

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):

Somoza, Maria E. “Gene network understanding and analysis.” 2016. Thesis, New Jersey Institute of Technology. Accessed March 07, 2021. https://digitalcommons.njit.edu/theses/279.

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

MLA Handbook (7th Edition):

Somoza, Maria E. “Gene network understanding and analysis.” 2016. Web. 07 Mar 2021.

Vancouver:

Somoza ME. Gene network understanding and analysis. [Internet] [Thesis]. New Jersey Institute of Technology; 2016. [cited 2021 Mar 07]. Available from: https://digitalcommons.njit.edu/theses/279.

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

Council of Science Editors:

Somoza ME. Gene network understanding and analysis. [Thesis]. New Jersey Institute of Technology; 2016. Available from: https://digitalcommons.njit.edu/theses/279

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


Univerzitet u Beogradu

18. Novović, Katarina, 1989- 14938471. Regulacija genske ekspresije i diverzitet CarO i Omp33-36 porina roda Acinetobacter spp.

Degree: Biološki fakultet, 2019, Univerzitet u Beogradu

Biologija - Molekularna biologija prokariota / Biology - Molecular biology of prokaryotes

Vrste roda Acinetobacter, pre svih Acinetobacter baumannii, su u poslednjih nekoliko decenija od… (more)

Subjects/Keywords: Acinetobacter; Acinetobacter baumannii; carbapenem resistance; porins; CarO; Omp33-36; gene expression regulation; trancriptional gene expression regulation; vaccines

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

APA (6th Edition):

Novović, Katarina, 1. 1. (2019). Regulacija genske ekspresije i diverzitet CarO i Omp33-36 porina roda Acinetobacter spp. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19563/bdef:Content/get

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):

Novović, Katarina, 1989- 14938471. “Regulacija genske ekspresije i diverzitet CarO i Omp33-36 porina roda Acinetobacter spp.” 2019. Thesis, Univerzitet u Beogradu. Accessed March 07, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:19563/bdef:Content/get.

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

MLA Handbook (7th Edition):

Novović, Katarina, 1989- 14938471. “Regulacija genske ekspresije i diverzitet CarO i Omp33-36 porina roda Acinetobacter spp.” 2019. Web. 07 Mar 2021.

Vancouver:

Novović, Katarina 11. Regulacija genske ekspresije i diverzitet CarO i Omp33-36 porina roda Acinetobacter spp. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2021 Mar 07]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19563/bdef:Content/get.

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

Council of Science Editors:

Novović, Katarina 11. Regulacija genske ekspresije i diverzitet CarO i Omp33-36 porina roda Acinetobacter spp. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19563/bdef:Content/get

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

19. Odye, Gweltas. Caractérisation fonctionnelle de la protéine ANKS3 impliquée dans les ciliopathies rénales et étude de son rôle dans la régulation des ARNs : Functional characterization of the ANKS3 protein involved in renal ciliopathies and study of its role in the RNAs regulation.

Degree: Docteur es, Biologie cellulaire, 2018, Sorbonne Paris Cité

 La Néphronophtise (NPH) est une néphropathie tubulo-interstitielle autosomique récessive, caractérisée par la présence d'une fibrose interstitielle massive et la formation de kystes. Elle est la… (more)

Subjects/Keywords: Cil primaire; Nephronophtise; Régulation ARN; Expression génique; Primary cilia; Nephronophtisis; MRNA regulation; Gene expression; 573.4

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APA (6th Edition):

Odye, G. (2018). Caractérisation fonctionnelle de la protéine ANKS3 impliquée dans les ciliopathies rénales et étude de son rôle dans la régulation des ARNs : Functional characterization of the ANKS3 protein involved in renal ciliopathies and study of its role in the RNAs regulation. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2018USPCB029

Chicago Manual of Style (16th Edition):

Odye, Gweltas. “Caractérisation fonctionnelle de la protéine ANKS3 impliquée dans les ciliopathies rénales et étude de son rôle dans la régulation des ARNs : Functional characterization of the ANKS3 protein involved in renal ciliopathies and study of its role in the RNAs regulation.” 2018. Doctoral Dissertation, Sorbonne Paris Cité. Accessed March 07, 2021. http://www.theses.fr/2018USPCB029.

MLA Handbook (7th Edition):

Odye, Gweltas. “Caractérisation fonctionnelle de la protéine ANKS3 impliquée dans les ciliopathies rénales et étude de son rôle dans la régulation des ARNs : Functional characterization of the ANKS3 protein involved in renal ciliopathies and study of its role in the RNAs regulation.” 2018. Web. 07 Mar 2021.

Vancouver:

Odye G. Caractérisation fonctionnelle de la protéine ANKS3 impliquée dans les ciliopathies rénales et étude de son rôle dans la régulation des ARNs : Functional characterization of the ANKS3 protein involved in renal ciliopathies and study of its role in the RNAs regulation. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2018. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2018USPCB029.

Council of Science Editors:

Odye G. Caractérisation fonctionnelle de la protéine ANKS3 impliquée dans les ciliopathies rénales et étude de son rôle dans la régulation des ARNs : Functional characterization of the ANKS3 protein involved in renal ciliopathies and study of its role in the RNAs regulation. [Doctoral Dissertation]. Sorbonne Paris Cité; 2018. Available from: http://www.theses.fr/2018USPCB029


University of Utah

20. Petersen, Jeannine Marie. Structural basis of DNA binding and autoinhibition for the eukaryotic transcription factor ETS-1;.

Degree: PhD, Oncological Sciences;, 1996, University of Utah

 The ets family of transcription factors represents a paradox in the study of DNA binding proteins. How can regulatory proteins that share the same DNA… (more)

Subjects/Keywords: Gene Expression Regulation; Eukaryotic Cells

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

APA (6th Edition):

Petersen, J. M. (1996). Structural basis of DNA binding and autoinhibition for the eukaryotic transcription factor ETS-1;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/892/rec/1247

Chicago Manual of Style (16th Edition):

Petersen, Jeannine Marie. “Structural basis of DNA binding and autoinhibition for the eukaryotic transcription factor ETS-1;.” 1996. Doctoral Dissertation, University of Utah. Accessed March 07, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/892/rec/1247.

MLA Handbook (7th Edition):

Petersen, Jeannine Marie. “Structural basis of DNA binding and autoinhibition for the eukaryotic transcription factor ETS-1;.” 1996. Web. 07 Mar 2021.

Vancouver:

Petersen JM. Structural basis of DNA binding and autoinhibition for the eukaryotic transcription factor ETS-1;. [Internet] [Doctoral dissertation]. University of Utah; 1996. [cited 2021 Mar 07]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/892/rec/1247.

Council of Science Editors:

Petersen JM. Structural basis of DNA binding and autoinhibition for the eukaryotic transcription factor ETS-1;. [Doctoral Dissertation]. University of Utah; 1996. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/892/rec/1247

21. DeBoer, Jason Todd. Proteomic Analyses of HIV-1 Infected T-cells and the Functional Characterization of Cyclophilin B During HIV-1 Infection.

Degree: PhD, Medical Microbiology and Immunology (graduate program), 2015, Creighton University

 The human immunodeficiency virus type 1 (HIV-1) lifecycle is complex and the virus interacts with many host cellular proteins for productive replication. Mass spectrometry analysis… (more)

Subjects/Keywords: HIV-1 – physiology; Gene Expression Regulation – immunology; Nuclear Proteins – metabolism

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

APA (6th Edition):

DeBoer, J. T. (2015). Proteomic Analyses of HIV-1 Infected T-cells and the Functional Characterization of Cyclophilin B During HIV-1 Infection. (Doctoral Dissertation). Creighton University. Retrieved from http://hdl.handle.net/10504/68567

Chicago Manual of Style (16th Edition):

DeBoer, Jason Todd. “Proteomic Analyses of HIV-1 Infected T-cells and the Functional Characterization of Cyclophilin B During HIV-1 Infection.” 2015. Doctoral Dissertation, Creighton University. Accessed March 07, 2021. http://hdl.handle.net/10504/68567.

MLA Handbook (7th Edition):

DeBoer, Jason Todd. “Proteomic Analyses of HIV-1 Infected T-cells and the Functional Characterization of Cyclophilin B During HIV-1 Infection.” 2015. Web. 07 Mar 2021.

Vancouver:

DeBoer JT. Proteomic Analyses of HIV-1 Infected T-cells and the Functional Characterization of Cyclophilin B During HIV-1 Infection. [Internet] [Doctoral dissertation]. Creighton University; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10504/68567.

Council of Science Editors:

DeBoer JT. Proteomic Analyses of HIV-1 Infected T-cells and the Functional Characterization of Cyclophilin B During HIV-1 Infection. [Doctoral Dissertation]. Creighton University; 2015. Available from: http://hdl.handle.net/10504/68567


University of Windsor

22. Komnenov, Dragana. Regulation of expression of CPB2, the gene encoding human thrombin activatable fibrinolysis inhibitor (TAFI): the role for post-transcriptional regulation.

Degree: PhD, Chemistry and Biochemistry, 2014, University of Windsor

  Disequilibrium between coagulation and fibrinolysis can lead to severe haemostatic disorders such as thrombosis and hemophilia. Thrombin-activable fibrinolysis inhibitor (TAFI) is a carboxypeptidase B-like… (more)

Subjects/Keywords: Cardiovascular disease; Coagulation; Fibrinolysis; Gene expression; Post-transcriptional regulation

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APA (6th Edition):

Komnenov, D. (2014). Regulation of expression of CPB2, the gene encoding human thrombin activatable fibrinolysis inhibitor (TAFI): the role for post-transcriptional regulation. (Doctoral Dissertation). University of Windsor. Retrieved from http://scholar.uwindsor.ca/etd/5213

Chicago Manual of Style (16th Edition):

Komnenov, Dragana. “Regulation of expression of CPB2, the gene encoding human thrombin activatable fibrinolysis inhibitor (TAFI): the role for post-transcriptional regulation.” 2014. Doctoral Dissertation, University of Windsor. Accessed March 07, 2021. http://scholar.uwindsor.ca/etd/5213.

MLA Handbook (7th Edition):

Komnenov, Dragana. “Regulation of expression of CPB2, the gene encoding human thrombin activatable fibrinolysis inhibitor (TAFI): the role for post-transcriptional regulation.” 2014. Web. 07 Mar 2021.

Vancouver:

Komnenov D. Regulation of expression of CPB2, the gene encoding human thrombin activatable fibrinolysis inhibitor (TAFI): the role for post-transcriptional regulation. [Internet] [Doctoral dissertation]. University of Windsor; 2014. [cited 2021 Mar 07]. Available from: http://scholar.uwindsor.ca/etd/5213.

Council of Science Editors:

Komnenov D. Regulation of expression of CPB2, the gene encoding human thrombin activatable fibrinolysis inhibitor (TAFI): the role for post-transcriptional regulation. [Doctoral Dissertation]. University of Windsor; 2014. Available from: http://scholar.uwindsor.ca/etd/5213


Penn State University

23. Horvath, Lindsay Marie. Deletion of an X-inactivation boundary disrupts adjacent gene silencing.

Degree: 2013, Penn State University

 In mammalian females, genes on one X chromosome are largely silenced by X-chromosome inactivation (XCI), although some “escape” XCI and are expressed from both X… (more)

Subjects/Keywords: X chromosome; gene expression; domain boundary; boundary regulation; X-chromosome inactivation

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

APA (6th Edition):

Horvath, L. M. (2013). Deletion of an X-inactivation boundary disrupts adjacent gene silencing. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/19799

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):

Horvath, Lindsay Marie. “Deletion of an X-inactivation boundary disrupts adjacent gene silencing.” 2013. Thesis, Penn State University. Accessed March 07, 2021. https://submit-etda.libraries.psu.edu/catalog/19799.

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

MLA Handbook (7th Edition):

Horvath, Lindsay Marie. “Deletion of an X-inactivation boundary disrupts adjacent gene silencing.” 2013. Web. 07 Mar 2021.

Vancouver:

Horvath LM. Deletion of an X-inactivation boundary disrupts adjacent gene silencing. [Internet] [Thesis]. Penn State University; 2013. [cited 2021 Mar 07]. Available from: https://submit-etda.libraries.psu.edu/catalog/19799.

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

Council of Science Editors:

Horvath LM. Deletion of an X-inactivation boundary disrupts adjacent gene silencing. [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/19799

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

24. Vetter, Ali Jean. Protein Acetylation and Regulation of CFTR Expression.

Degree: 2015, University of Texas Southwestern Medical Center

 Cystic Fibrosis (CF) is an autosomal recessive disease caused by a loss of function of a chloride channel encoded by the cystic fibrosis conductance regulator… (more)

Subjects/Keywords: Cystic Fibrosis Transmembrane Conductance Regulator; Gene Expression Regulation; N-Terminal Acetyltransferases

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

APA (6th Edition):

Vetter, A. J. (2015). Protein Acetylation and Regulation of CFTR Expression. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5289

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):

Vetter, Ali Jean. “Protein Acetylation and Regulation of CFTR Expression.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed March 07, 2021. http://hdl.handle.net/2152.5/5289.

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

MLA Handbook (7th Edition):

Vetter, Ali Jean. “Protein Acetylation and Regulation of CFTR Expression.” 2015. Web. 07 Mar 2021.

Vancouver:

Vetter AJ. Protein Acetylation and Regulation of CFTR Expression. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2152.5/5289.

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

Council of Science Editors:

Vetter AJ. Protein Acetylation and Regulation of CFTR Expression. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/5289

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

25. Uruena, Ana Cristina. Examining the Role of PRDM13 in Dorsal Interneuron Specification.

Degree: 2016, University of Texas Southwestern Medical Center

 PTF1A is a transcription factor transiently expressed as neural progenitor cells become post-mitotic and begin to express neuronal specific genes. PTF1A specifies these cells to… (more)

Subjects/Keywords: Gene Expression Regulation, Developmental; Neurons; Regulatory Sequences, Nucleic Acid; Transcription Factors

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APA (6th Edition):

Uruena, A. C. (2016). Examining the Role of PRDM13 in Dorsal Interneuron Specification. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/5745

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):

Uruena, Ana Cristina. “Examining the Role of PRDM13 in Dorsal Interneuron Specification.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed March 07, 2021. http://hdl.handle.net/2152.5/5745.

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

MLA Handbook (7th Edition):

Uruena, Ana Cristina. “Examining the Role of PRDM13 in Dorsal Interneuron Specification.” 2016. Web. 07 Mar 2021.

Vancouver:

Uruena AC. Examining the Role of PRDM13 in Dorsal Interneuron Specification. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2152.5/5745.

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

Council of Science Editors:

Uruena AC. Examining the Role of PRDM13 in Dorsal Interneuron Specification. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/5745

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

26. Carrasco, Yazmin Paulina. Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes.

Degree: 2013, University of Texas Southwestern Medical Center

 Aware of the important role that terrestrial microbial natural products play in the discovery of therapeutics and the decrease in rate of discovery of new… (more)

Subjects/Keywords: Gene Expression Regulation, Neoplastic; Fatty Acids, Unsaturated; Receptors, Cytoplasmic and Nuclear

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APA (6th Edition):

Carrasco, Y. P. (2013). Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2716

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):

Carrasco, Yazmin Paulina. “Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed March 07, 2021. http://hdl.handle.net/2152.5/2716.

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

MLA Handbook (7th Edition):

Carrasco, Yazmin Paulina. “Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes.” 2013. Web. 07 Mar 2021.

Vancouver:

Carrasco YP. Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2152.5/2716.

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

Council of Science Editors:

Carrasco YP. Natural Products as Selective Chemotherapeutic Agents and as Chemical Probes to Understand Biological Processes. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/2716

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

27. Bodemann, Brian Oliver. Ral G-Proteins and the Exocyst Complex are Mediators of the Cellular Response to Nutrients.

Degree: 2012, University of Texas Southwestern Medical Center

 The small G-proteins, RalA and RalB, are important mediators of cellular responses to viral infection and nutrient availability. Prior work has demonstrated that the exocyst… (more)

Subjects/Keywords: ral GTP-Binding Proteins; Gene Expression Regulation, Enzymologic; Neoplasms

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APA (6th Edition):

Bodemann, B. O. (2012). Ral G-Proteins and the Exocyst Complex are Mediators of the Cellular Response to Nutrients. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1015

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):

Bodemann, Brian Oliver. “Ral G-Proteins and the Exocyst Complex are Mediators of the Cellular Response to Nutrients.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed March 07, 2021. http://hdl.handle.net/2152.5/1015.

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

MLA Handbook (7th Edition):

Bodemann, Brian Oliver. “Ral G-Proteins and the Exocyst Complex are Mediators of the Cellular Response to Nutrients.” 2012. Web. 07 Mar 2021.

Vancouver:

Bodemann BO. Ral G-Proteins and the Exocyst Complex are Mediators of the Cellular Response to Nutrients. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2152.5/1015.

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

Council of Science Editors:

Bodemann BO. Ral G-Proteins and the Exocyst Complex are Mediators of the Cellular Response to Nutrients. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1015

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

28. Collins, Katie Anne. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.

Degree: 2014, University of Texas Southwestern Medical Center

 Autism is a neurological disorder characterized by repetetive behaviors, social anxiety and verbal and non-verbal communication. Fragile X Syndrome (FXS) is the most common genetic… (more)

Subjects/Keywords: Carrier Proteins; Fragile X Syndrome; Gene Expression Regulation; Receptors, Metabotropic Glutamate

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APA (6th Edition):

Collins, K. A. (2014). The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3308

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):

Collins, Katie Anne. “The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed March 07, 2021. http://hdl.handle.net/2152.5/3308.

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

MLA Handbook (7th Edition):

Collins, Katie Anne. “The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders.” 2014. Web. 07 Mar 2021.

Vancouver:

Collins KA. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2152.5/3308.

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

Council of Science Editors:

Collins KA. The Role of Homer Scaffolding to Metabotropic Glutamate Receptor 5 in the Mouse Models of Neurodevelopement Disorders. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3308

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

29. Paulson, Vera Ashley. High-Resolution Array Comparative Genomic Hybridization Identifies Common Targets in Rhabdomyosarcoma.

Degree: 2012, University of Texas Southwestern Medical Center

 Rhabdomyosarcoma (RMS) accounts for nearly 50 percent of the soft tissue sarcomas that affect children. There are two major histological variants, alveolar (ARMS) and embryonal… (more)

Subjects/Keywords: Rhabdomyosarcoma; Gene Expression Regulation, Neoplastic; Receptor, Fibroblast Growth Factor, Type 4

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

APA (6th Edition):

Paulson, V. A. (2012). High-Resolution Array Comparative Genomic Hybridization Identifies Common Targets in Rhabdomyosarcoma. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1112

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):

Paulson, Vera Ashley. “High-Resolution Array Comparative Genomic Hybridization Identifies Common Targets in Rhabdomyosarcoma.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed March 07, 2021. http://hdl.handle.net/2152.5/1112.

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

MLA Handbook (7th Edition):

Paulson, Vera Ashley. “High-Resolution Array Comparative Genomic Hybridization Identifies Common Targets in Rhabdomyosarcoma.” 2012. Web. 07 Mar 2021.

Vancouver:

Paulson VA. High-Resolution Array Comparative Genomic Hybridization Identifies Common Targets in Rhabdomyosarcoma. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2152.5/1112.

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

Council of Science Editors:

Paulson VA. High-Resolution Array Comparative Genomic Hybridization Identifies Common Targets in Rhabdomyosarcoma. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1112

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. Beane, Randall L. Silencing Transcription: Promoter-Targeted Oligonucleotides Bind Chromosomal DNA Inside Cells.

Degree: 2009, University of Texas Southwestern Medical Center

 Aberrant gene expression can lead to multiple disease-states that can be difficult or impossible to treat using traditional small-molecule medications. An alternative approach to treating… (more)

Subjects/Keywords: Gene Expression Regulation; DNA; Oligonucleotides

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

APA (6th Edition):

Beane, R. L. (2009). Silencing Transcription: Promoter-Targeted Oligonucleotides Bind Chromosomal DNA Inside Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/673

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):

Beane, Randall L. “Silencing Transcription: Promoter-Targeted Oligonucleotides Bind Chromosomal DNA Inside Cells.” 2009. Thesis, University of Texas Southwestern Medical Center. Accessed March 07, 2021. http://hdl.handle.net/2152.5/673.

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

MLA Handbook (7th Edition):

Beane, Randall L. “Silencing Transcription: Promoter-Targeted Oligonucleotides Bind Chromosomal DNA Inside Cells.” 2009. Web. 07 Mar 2021.

Vancouver:

Beane RL. Silencing Transcription: Promoter-Targeted Oligonucleotides Bind Chromosomal DNA Inside Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2009. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2152.5/673.

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

Council of Science Editors:

Beane RL. Silencing Transcription: Promoter-Targeted Oligonucleotides Bind Chromosomal DNA Inside Cells. [Thesis]. University of Texas Southwestern Medical Center; 2009. Available from: http://hdl.handle.net/2152.5/673

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

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