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You searched for subject:(Medical Molecular Biology). Showing records 1 – 30 of 514 total matches.

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McMaster University

1. Ghayur, Ayesha. ROLE OF TRANSFORMING GROWTH FACTOR BETA IN PROTEINURIA.

Degree: PhD, 2013, McMaster University

The incidence and prevalence of people suffering from end stage renal disease is increasing. Proteinuria, particularly the presence of albumin in urine is concerning… (more)

Subjects/Keywords: Medical Molecular Biology; Medical Molecular Biology

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APA (6th Edition):

Ghayur, A. (2013). ROLE OF TRANSFORMING GROWTH FACTOR BETA IN PROTEINURIA. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/15252

Chicago Manual of Style (16th Edition):

Ghayur, Ayesha. “ROLE OF TRANSFORMING GROWTH FACTOR BETA IN PROTEINURIA.” 2013. Doctoral Dissertation, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/15252.

MLA Handbook (7th Edition):

Ghayur, Ayesha. “ROLE OF TRANSFORMING GROWTH FACTOR BETA IN PROTEINURIA.” 2013. Web. 18 Jan 2021.

Vancouver:

Ghayur A. ROLE OF TRANSFORMING GROWTH FACTOR BETA IN PROTEINURIA. [Internet] [Doctoral dissertation]. McMaster University; 2013. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/15252.

Council of Science Editors:

Ghayur A. ROLE OF TRANSFORMING GROWTH FACTOR BETA IN PROTEINURIA. [Doctoral Dissertation]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/15252


University of Vermont

2. Director, Laura Taylor. A Novel Approach For The Identification of Cytoskeletal and Adhesion A-Kinase Anchoring Proteins.

Degree: MS, Cellular, Molecular and Biomedical Sciences, 2014, University of Vermont

  A-kinase anchoring proteins (AKAPs) are signaling scaffolds which provide spatial and temporal organization of signaling pathways in discrete subcellular compartments. Through tethering the cyclic-AMP… (more)

Subjects/Keywords: Medical Cell Biology; Molecular Biology

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APA (6th Edition):

Director, L. T. (2014). A Novel Approach For The Identification of Cytoskeletal and Adhesion A-Kinase Anchoring Proteins. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/264

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):

Director, Laura Taylor. “A Novel Approach For The Identification of Cytoskeletal and Adhesion A-Kinase Anchoring Proteins.” 2014. Thesis, University of Vermont. Accessed January 18, 2021. https://scholarworks.uvm.edu/graddis/264.

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

MLA Handbook (7th Edition):

Director, Laura Taylor. “A Novel Approach For The Identification of Cytoskeletal and Adhesion A-Kinase Anchoring Proteins.” 2014. Web. 18 Jan 2021.

Vancouver:

Director LT. A Novel Approach For The Identification of Cytoskeletal and Adhesion A-Kinase Anchoring Proteins. [Internet] [Thesis]. University of Vermont; 2014. [cited 2021 Jan 18]. Available from: https://scholarworks.uvm.edu/graddis/264.

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

Council of Science Editors:

Director LT. A Novel Approach For The Identification of Cytoskeletal and Adhesion A-Kinase Anchoring Proteins. [Thesis]. University of Vermont; 2014. Available from: https://scholarworks.uvm.edu/graddis/264

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


Columbia University

3. Kuo, Chao-Ling. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.

Degree: 2011, Columbia University

 Atherosclerosis, the primary cause of heart attack, stroke, and peripheral vascular disease, is genetically complex and the genes that confer cardiovascular risk remain largely unknown.… (more)

Subjects/Keywords: Medical sciences; Genetics; Molecular biology

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APA (6th Edition):

Kuo, C. (2011). Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8CV4QXC

Chicago Manual of Style (16th Edition):

Kuo, Chao-Ling. “Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.” 2011. Doctoral Dissertation, Columbia University. Accessed January 18, 2021. https://doi.org/10.7916/D8CV4QXC.

MLA Handbook (7th Edition):

Kuo, Chao-Ling. “Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:.” 2011. Web. 18 Jan 2021.

Vancouver:

Kuo C. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. [Internet] [Doctoral dissertation]. Columbia University; 2011. [cited 2021 Jan 18]. Available from: https://doi.org/10.7916/D8CV4QXC.

Council of Science Editors:

Kuo C. Characterization ofAthsq1, an Atherosclerosis Modifier Locus on Mouse Chromosome 4:. [Doctoral Dissertation]. Columbia University; 2011. Available from: https://doi.org/10.7916/D8CV4QXC


University of Western Ontario

4. Wijewardhana, Chanuka. Virally Packaged RNA in Virus-Like Particle Vaccines Enhances Antigenicity and Augments Latency Reversal of HIV-1.

Degree: 2019, University of Western Ontario

 Introduction: Since Human Immunodeficiency Virus (HIV)-1 was determined to be the etiological agent behind acquired immunodeficiency syndrome (AIDS) in 1983, numerous attempts at a cure… (more)

Subjects/Keywords: Medical Immunology; Medical Molecular Biology; Virus Diseases

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APA (6th Edition):

Wijewardhana, C. (2019). Virally Packaged RNA in Virus-Like Particle Vaccines Enhances Antigenicity and Augments Latency Reversal of HIV-1. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6642

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):

Wijewardhana, Chanuka. “Virally Packaged RNA in Virus-Like Particle Vaccines Enhances Antigenicity and Augments Latency Reversal of HIV-1.” 2019. Thesis, University of Western Ontario. Accessed January 18, 2021. https://ir.lib.uwo.ca/etd/6642.

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

MLA Handbook (7th Edition):

Wijewardhana, Chanuka. “Virally Packaged RNA in Virus-Like Particle Vaccines Enhances Antigenicity and Augments Latency Reversal of HIV-1.” 2019. Web. 18 Jan 2021.

Vancouver:

Wijewardhana C. Virally Packaged RNA in Virus-Like Particle Vaccines Enhances Antigenicity and Augments Latency Reversal of HIV-1. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2021 Jan 18]. Available from: https://ir.lib.uwo.ca/etd/6642.

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

Council of Science Editors:

Wijewardhana C. Virally Packaged RNA in Virus-Like Particle Vaccines Enhances Antigenicity and Augments Latency Reversal of HIV-1. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6642

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


McMaster University

5. Gabriel, Kathleen. Regulation of the tumour suppressor PTEN through exosomes.

Degree: MSc, 2013, McMaster University

PTEN is a potent tumour suppressor protein. Aggressive and metastatic prostate cancer (PC) is associated with a reduction or loss of PTEN expression. PTEN… (more)

Subjects/Keywords: prostate cancer; PTEN; exosomes; microvesicles; Medical Molecular Biology; Medical Molecular Biology

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APA (6th Edition):

Gabriel, K. (2013). Regulation of the tumour suppressor PTEN through exosomes. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/13591

Chicago Manual of Style (16th Edition):

Gabriel, Kathleen. “Regulation of the tumour suppressor PTEN through exosomes.” 2013. Masters Thesis, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/13591.

MLA Handbook (7th Edition):

Gabriel, Kathleen. “Regulation of the tumour suppressor PTEN through exosomes.” 2013. Web. 18 Jan 2021.

Vancouver:

Gabriel K. Regulation of the tumour suppressor PTEN through exosomes. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/13591.

Council of Science Editors:

Gabriel K. Regulation of the tumour suppressor PTEN through exosomes. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13591

6. Guen, Vincent. Découverte de la protéine kinase CDK10 / Cycline M et exploration de ses fonctions biologiques en lien avec le syndrome STAR : Discovery of the protein kinase CDK10 / Cyclin M and exploration of its biological functions linked to STAR syndrome.

Degree: Docteur es, Biologie, 2013, Rennes 1

Les kinases dépendantes des cyclines (CDKs) sont les régulateurs essentiels du cycle cellulaire. Au sein de la famille des cyclines, les fonctions de la cycline… (more)

Subjects/Keywords: Sciences médicales; Biologie moléculaire et cellulaire; Medical sciences; Molecular and cellular biology

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APA (6th Edition):

Guen, V. (2013). Découverte de la protéine kinase CDK10 / Cycline M et exploration de ses fonctions biologiques en lien avec le syndrome STAR : Discovery of the protein kinase CDK10 / Cyclin M and exploration of its biological functions linked to STAR syndrome. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2013REN1S084

Chicago Manual of Style (16th Edition):

Guen, Vincent. “Découverte de la protéine kinase CDK10 / Cycline M et exploration de ses fonctions biologiques en lien avec le syndrome STAR : Discovery of the protein kinase CDK10 / Cyclin M and exploration of its biological functions linked to STAR syndrome.” 2013. Doctoral Dissertation, Rennes 1. Accessed January 18, 2021. http://www.theses.fr/2013REN1S084.

MLA Handbook (7th Edition):

Guen, Vincent. “Découverte de la protéine kinase CDK10 / Cycline M et exploration de ses fonctions biologiques en lien avec le syndrome STAR : Discovery of the protein kinase CDK10 / Cyclin M and exploration of its biological functions linked to STAR syndrome.” 2013. Web. 18 Jan 2021.

Vancouver:

Guen V. Découverte de la protéine kinase CDK10 / Cycline M et exploration de ses fonctions biologiques en lien avec le syndrome STAR : Discovery of the protein kinase CDK10 / Cyclin M and exploration of its biological functions linked to STAR syndrome. [Internet] [Doctoral dissertation]. Rennes 1; 2013. [cited 2021 Jan 18]. Available from: http://www.theses.fr/2013REN1S084.

Council of Science Editors:

Guen V. Découverte de la protéine kinase CDK10 / Cycline M et exploration de ses fonctions biologiques en lien avec le syndrome STAR : Discovery of the protein kinase CDK10 / Cyclin M and exploration of its biological functions linked to STAR syndrome. [Doctoral Dissertation]. Rennes 1; 2013. Available from: http://www.theses.fr/2013REN1S084


University of Nevada – Las Vegas

7. McKenna, Austin Joseph. Rapid Evolution of Starvation Resistance in Drosophila: Physiological and Molecular Mechanisms.

Degree: PhD, Life Sciences, 2020, University of Nevada – Las Vegas

  The Gibbs lab has maintained starvation-selected Drosophila melanogaster for >130 generations. These starvation-selected flies evolved an obese phenotype with a suite of physiological differences… (more)

Subjects/Keywords: Biology; Medical Physiology; Molecular Biology; Physiology

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APA (6th Edition):

McKenna, A. J. (2020). Rapid Evolution of Starvation Resistance in Drosophila: Physiological and Molecular Mechanisms. (Doctoral Dissertation). University of Nevada – Las Vegas. Retrieved from https://digitalscholarship.unlv.edu/thesesdissertations/3928

Chicago Manual of Style (16th Edition):

McKenna, Austin Joseph. “Rapid Evolution of Starvation Resistance in Drosophila: Physiological and Molecular Mechanisms.” 2020. Doctoral Dissertation, University of Nevada – Las Vegas. Accessed January 18, 2021. https://digitalscholarship.unlv.edu/thesesdissertations/3928.

MLA Handbook (7th Edition):

McKenna, Austin Joseph. “Rapid Evolution of Starvation Resistance in Drosophila: Physiological and Molecular Mechanisms.” 2020. Web. 18 Jan 2021.

Vancouver:

McKenna AJ. Rapid Evolution of Starvation Resistance in Drosophila: Physiological and Molecular Mechanisms. [Internet] [Doctoral dissertation]. University of Nevada – Las Vegas; 2020. [cited 2021 Jan 18]. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/3928.

Council of Science Editors:

McKenna AJ. Rapid Evolution of Starvation Resistance in Drosophila: Physiological and Molecular Mechanisms. [Doctoral Dissertation]. University of Nevada – Las Vegas; 2020. Available from: https://digitalscholarship.unlv.edu/thesesdissertations/3928


Purdue University

8. Zhu, Wenhan. Host cell death in Legionella pneumophila pathogenesis and immunity.

Degree: PhD, Biological Science, 2014, Purdue University

  Legionella pneumophila is an intracellular pathogen that causes a severe, atypical pneumonia termed Legionnaires' disease. Upon entering the host cell, L. pneumophila resides in… (more)

Subjects/Keywords: Biology; Medical Immunology; Microbiology; Molecular Biology

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APA (6th Edition):

Zhu, W. (2014). Host cell death in Legionella pneumophila pathogenesis and immunity. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/405

Chicago Manual of Style (16th Edition):

Zhu, Wenhan. “Host cell death in Legionella pneumophila pathogenesis and immunity.” 2014. Doctoral Dissertation, Purdue University. Accessed January 18, 2021. https://docs.lib.purdue.edu/open_access_dissertations/405.

MLA Handbook (7th Edition):

Zhu, Wenhan. “Host cell death in Legionella pneumophila pathogenesis and immunity.” 2014. Web. 18 Jan 2021.

Vancouver:

Zhu W. Host cell death in Legionella pneumophila pathogenesis and immunity. [Internet] [Doctoral dissertation]. Purdue University; 2014. [cited 2021 Jan 18]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/405.

Council of Science Editors:

Zhu W. Host cell death in Legionella pneumophila pathogenesis and immunity. [Doctoral Dissertation]. Purdue University; 2014. Available from: https://docs.lib.purdue.edu/open_access_dissertations/405


McMaster University

9. Mustafa, Maria. THE ROLE OF STEROL REGULATORY ELEMENT BINDING PROTEIN (SREBP) IN KIDNEY FIBROSIS.

Degree: MSc, 2013, McMaster University

There has been a steady increase in the number of patients with chronic kidney disease. The etiology has been linked to excessive fibrosis progression… (more)

Subjects/Keywords: SREBP; Apoptosis; Fibrosis; Tubular cells; UUO; Fatostatin; Medical Molecular Biology; Medical Physiology; Medical Molecular Biology

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APA (6th Edition):

Mustafa, M. (2013). THE ROLE OF STEROL REGULATORY ELEMENT BINDING PROTEIN (SREBP) IN KIDNEY FIBROSIS. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15322

Chicago Manual of Style (16th Edition):

Mustafa, Maria. “THE ROLE OF STEROL REGULATORY ELEMENT BINDING PROTEIN (SREBP) IN KIDNEY FIBROSIS.” 2013. Masters Thesis, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/15322.

MLA Handbook (7th Edition):

Mustafa, Maria. “THE ROLE OF STEROL REGULATORY ELEMENT BINDING PROTEIN (SREBP) IN KIDNEY FIBROSIS.” 2013. Web. 18 Jan 2021.

Vancouver:

Mustafa M. THE ROLE OF STEROL REGULATORY ELEMENT BINDING PROTEIN (SREBP) IN KIDNEY FIBROSIS. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/15322.

Council of Science Editors:

Mustafa M. THE ROLE OF STEROL REGULATORY ELEMENT BINDING PROTEIN (SREBP) IN KIDNEY FIBROSIS. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/15322


University of Iowa

10. Dajani, Rana Basem. Innate immune responses in the lung and liver.

Degree: PhD, Molecular Biology, 2005, University of Iowa

  The innate immune system provides nonspecific defenses against pathogens. Many diseases occur because of malfunctions in the innate immune system. In the present thesis,… (more)

Subjects/Keywords: Medical Molecular Biology; Molecular Biology

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APA (6th Edition):

Dajani, R. B. (2005). Innate immune responses in the lung and liver. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/103

Chicago Manual of Style (16th Edition):

Dajani, Rana Basem. “Innate immune responses in the lung and liver.” 2005. Doctoral Dissertation, University of Iowa. Accessed January 18, 2021. https://ir.uiowa.edu/etd/103.

MLA Handbook (7th Edition):

Dajani, Rana Basem. “Innate immune responses in the lung and liver.” 2005. Web. 18 Jan 2021.

Vancouver:

Dajani RB. Innate immune responses in the lung and liver. [Internet] [Doctoral dissertation]. University of Iowa; 2005. [cited 2021 Jan 18]. Available from: https://ir.uiowa.edu/etd/103.

Council of Science Editors:

Dajani RB. Innate immune responses in the lung and liver. [Doctoral Dissertation]. University of Iowa; 2005. Available from: https://ir.uiowa.edu/etd/103


University of Iowa

11. Slevin, Michael Keith. Post transcriptional regulation of cyclin E during the embryonic development of Xenopus laevis.

Degree: PhD, Molecular and Cellular Biology, 2006, University of Iowa

  The embryonic cell cycle of Xenopus laevis consists of rapid oscillations between S and M phase occurring in the absence of gap phases and… (more)

Subjects/Keywords: Medical Molecular Biology; Molecular Biology

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APA (6th Edition):

Slevin, M. K. (2006). Post transcriptional regulation of cyclin E during the embryonic development of Xenopus laevis. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/74

Chicago Manual of Style (16th Edition):

Slevin, Michael Keith. “Post transcriptional regulation of cyclin E during the embryonic development of Xenopus laevis.” 2006. Doctoral Dissertation, University of Iowa. Accessed January 18, 2021. https://ir.uiowa.edu/etd/74.

MLA Handbook (7th Edition):

Slevin, Michael Keith. “Post transcriptional regulation of cyclin E during the embryonic development of Xenopus laevis.” 2006. Web. 18 Jan 2021.

Vancouver:

Slevin MK. Post transcriptional regulation of cyclin E during the embryonic development of Xenopus laevis. [Internet] [Doctoral dissertation]. University of Iowa; 2006. [cited 2021 Jan 18]. Available from: https://ir.uiowa.edu/etd/74.

Council of Science Editors:

Slevin MK. Post transcriptional regulation of cyclin E during the embryonic development of Xenopus laevis. [Doctoral Dissertation]. University of Iowa; 2006. Available from: https://ir.uiowa.edu/etd/74


McMaster University

12. Chew, Tracy. THE ROLE OF INTERFERON REGULATORY FACTOR 3 IN THE INNATE ANTIVIRAL RESPONSE.

Degree: PhD, 2012, McMaster University

The transcription factor interferon (IFN) regulatory factor 3 (IRF-3) plays a central role in the innate immune response to viral stimulation. IRF-3 participates in… (more)

Subjects/Keywords: innate immunity; virology; signalling; cell biology; molecular biology; cytokines; Medical Cell Biology; Medical Cell Biology

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APA (6th Edition):

Chew, T. (2012). THE ROLE OF INTERFERON REGULATORY FACTOR 3 IN THE INNATE ANTIVIRAL RESPONSE. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12055

Chicago Manual of Style (16th Edition):

Chew, Tracy. “THE ROLE OF INTERFERON REGULATORY FACTOR 3 IN THE INNATE ANTIVIRAL RESPONSE.” 2012. Doctoral Dissertation, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/12055.

MLA Handbook (7th Edition):

Chew, Tracy. “THE ROLE OF INTERFERON REGULATORY FACTOR 3 IN THE INNATE ANTIVIRAL RESPONSE.” 2012. Web. 18 Jan 2021.

Vancouver:

Chew T. THE ROLE OF INTERFERON REGULATORY FACTOR 3 IN THE INNATE ANTIVIRAL RESPONSE. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/12055.

Council of Science Editors:

Chew T. THE ROLE OF INTERFERON REGULATORY FACTOR 3 IN THE INNATE ANTIVIRAL RESPONSE. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12055


Loyola University Chicago

13. Novicki, Thomas Joseph. The Isolation and Characterization of pLV22a, a Mobilizable Plasmid from Bacteroides Fragilis.

Degree: PhD, Molecular Biology, 1997, Loyola University Chicago

Subjects/Keywords: Medical Molecular Biology

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APA (6th Edition):

Novicki, T. J. (1997). The Isolation and Characterization of pLV22a, a Mobilizable Plasmid from Bacteroides Fragilis. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/3413

Chicago Manual of Style (16th Edition):

Novicki, Thomas Joseph. “The Isolation and Characterization of pLV22a, a Mobilizable Plasmid from Bacteroides Fragilis.” 1997. Doctoral Dissertation, Loyola University Chicago. Accessed January 18, 2021. https://ecommons.luc.edu/luc_diss/3413.

MLA Handbook (7th Edition):

Novicki, Thomas Joseph. “The Isolation and Characterization of pLV22a, a Mobilizable Plasmid from Bacteroides Fragilis.” 1997. Web. 18 Jan 2021.

Vancouver:

Novicki TJ. The Isolation and Characterization of pLV22a, a Mobilizable Plasmid from Bacteroides Fragilis. [Internet] [Doctoral dissertation]. Loyola University Chicago; 1997. [cited 2021 Jan 18]. Available from: https://ecommons.luc.edu/luc_diss/3413.

Council of Science Editors:

Novicki TJ. The Isolation and Characterization of pLV22a, a Mobilizable Plasmid from Bacteroides Fragilis. [Doctoral Dissertation]. Loyola University Chicago; 1997. Available from: https://ecommons.luc.edu/luc_diss/3413


Loyola University Chicago

14. Applequist, Steven E. NORF1, a Putative Human Group I RNA Helicase That Regulates Nonsense MRNA Levels.

Degree: PhD, Molecular Biology, 1997, Loyola University Chicago

Subjects/Keywords: Medical Molecular Biology

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APA (6th Edition):

Applequist, S. E. (1997). NORF1, a Putative Human Group I RNA Helicase That Regulates Nonsense MRNA Levels. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/3415

Chicago Manual of Style (16th Edition):

Applequist, Steven E. “NORF1, a Putative Human Group I RNA Helicase That Regulates Nonsense MRNA Levels.” 1997. Doctoral Dissertation, Loyola University Chicago. Accessed January 18, 2021. https://ecommons.luc.edu/luc_diss/3415.

MLA Handbook (7th Edition):

Applequist, Steven E. “NORF1, a Putative Human Group I RNA Helicase That Regulates Nonsense MRNA Levels.” 1997. Web. 18 Jan 2021.

Vancouver:

Applequist SE. NORF1, a Putative Human Group I RNA Helicase That Regulates Nonsense MRNA Levels. [Internet] [Doctoral dissertation]. Loyola University Chicago; 1997. [cited 2021 Jan 18]. Available from: https://ecommons.luc.edu/luc_diss/3415.

Council of Science Editors:

Applequist SE. NORF1, a Putative Human Group I RNA Helicase That Regulates Nonsense MRNA Levels. [Doctoral Dissertation]. Loyola University Chicago; 1997. Available from: https://ecommons.luc.edu/luc_diss/3415


Loyola University Chicago

15. Grutkoski, Patricia S. Role of TGF-† in Heart Development: Analysis of the Type II TGF-† Receptor.

Degree: PhD, Molecular Biology, 1997, Loyola University Chicago

Subjects/Keywords: Medical Molecular Biology

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APA (6th Edition):

Grutkoski, P. S. (1997). Role of TGF-† in Heart Development: Analysis of the Type II TGF-† Receptor. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/3423

Chicago Manual of Style (16th Edition):

Grutkoski, Patricia S. “Role of TGF-† in Heart Development: Analysis of the Type II TGF-† Receptor.” 1997. Doctoral Dissertation, Loyola University Chicago. Accessed January 18, 2021. https://ecommons.luc.edu/luc_diss/3423.

MLA Handbook (7th Edition):

Grutkoski, Patricia S. “Role of TGF-† in Heart Development: Analysis of the Type II TGF-† Receptor.” 1997. Web. 18 Jan 2021.

Vancouver:

Grutkoski PS. Role of TGF-† in Heart Development: Analysis of the Type II TGF-† Receptor. [Internet] [Doctoral dissertation]. Loyola University Chicago; 1997. [cited 2021 Jan 18]. Available from: https://ecommons.luc.edu/luc_diss/3423.

Council of Science Editors:

Grutkoski PS. Role of TGF-† in Heart Development: Analysis of the Type II TGF-† Receptor. [Doctoral Dissertation]. Loyola University Chicago; 1997. Available from: https://ecommons.luc.edu/luc_diss/3423


Columbia University

16. Kumar, Brahma Vencel. Identification and characterization of tissue-resident memory T cells in humans.

Degree: 2018, Columbia University

 Memory T cells are critical for maintaining lifelong immunity by protecting against reinfection with previously encountered pathogens. In recent years, a subset of memory T… (more)

Subjects/Keywords: Immunology; T cells; Medical sciences; Molecular biology

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APA (6th Edition):

Kumar, B. V. (2018). Identification and characterization of tissue-resident memory T cells in humans. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8Q2563Z

Chicago Manual of Style (16th Edition):

Kumar, Brahma Vencel. “Identification and characterization of tissue-resident memory T cells in humans.” 2018. Doctoral Dissertation, Columbia University. Accessed January 18, 2021. https://doi.org/10.7916/D8Q2563Z.

MLA Handbook (7th Edition):

Kumar, Brahma Vencel. “Identification and characterization of tissue-resident memory T cells in humans.” 2018. Web. 18 Jan 2021.

Vancouver:

Kumar BV. Identification and characterization of tissue-resident memory T cells in humans. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2021 Jan 18]. Available from: https://doi.org/10.7916/D8Q2563Z.

Council of Science Editors:

Kumar BV. Identification and characterization of tissue-resident memory T cells in humans. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8Q2563Z


University of Lund

17. Moraghebi, Roksana. The Effects of Genetic and Epigenetic Variation on Human Pluripotent Stem Cell Differentiation.

Degree: 2017, University of Lund

 Human pluripotent stem cells (PSCs) are widely used for studying embryonic development, disease modelling, drug discovery and cell therapy development. Using human PSCs as a… (more)

Subjects/Keywords: Medical Genetics; Cell and Molecular Biology

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

APA (6th Edition):

Moraghebi, R. (2017). The Effects of Genetic and Epigenetic Variation on Human Pluripotent Stem Cell Differentiation. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/f0fcdff9-cdd7-4308-828f-827992336095 ; https://portal.research.lu.se/ws/files/29953955/Roksana_Moraghebi_Thesis.pdf

Chicago Manual of Style (16th Edition):

Moraghebi, Roksana. “The Effects of Genetic and Epigenetic Variation on Human Pluripotent Stem Cell Differentiation.” 2017. Doctoral Dissertation, University of Lund. Accessed January 18, 2021. https://lup.lub.lu.se/record/f0fcdff9-cdd7-4308-828f-827992336095 ; https://portal.research.lu.se/ws/files/29953955/Roksana_Moraghebi_Thesis.pdf.

MLA Handbook (7th Edition):

Moraghebi, Roksana. “The Effects of Genetic and Epigenetic Variation on Human Pluripotent Stem Cell Differentiation.” 2017. Web. 18 Jan 2021.

Vancouver:

Moraghebi R. The Effects of Genetic and Epigenetic Variation on Human Pluripotent Stem Cell Differentiation. [Internet] [Doctoral dissertation]. University of Lund; 2017. [cited 2021 Jan 18]. Available from: https://lup.lub.lu.se/record/f0fcdff9-cdd7-4308-828f-827992336095 ; https://portal.research.lu.se/ws/files/29953955/Roksana_Moraghebi_Thesis.pdf.

Council of Science Editors:

Moraghebi R. The Effects of Genetic and Epigenetic Variation on Human Pluripotent Stem Cell Differentiation. [Doctoral Dissertation]. University of Lund; 2017. Available from: https://lup.lub.lu.se/record/f0fcdff9-cdd7-4308-828f-827992336095 ; https://portal.research.lu.se/ws/files/29953955/Roksana_Moraghebi_Thesis.pdf


McMaster University

18. Verschoor, Meghan L. The Role of the Transcription Factor Ets-1 in Mitochondrial Metabolism and Oxidative Stress.

Degree: PhD, 2013, McMaster University

Normal cellular energy metabolism is fundamentally altered in cancer cells to facilitate rapid production of new cellular components, thereby enabling uncontrolled cell growth. Specifically,… (more)

Subjects/Keywords: Ovarian cancer; breast cancer; genomics; glutathione; glycolysis; Medical Molecular Biology; Medical Molecular Biology

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

APA (6th Edition):

Verschoor, M. L. (2013). The Role of the Transcription Factor Ets-1 in Mitochondrial Metabolism and Oxidative Stress. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/13152

Chicago Manual of Style (16th Edition):

Verschoor, Meghan L. “The Role of the Transcription Factor Ets-1 in Mitochondrial Metabolism and Oxidative Stress.” 2013. Doctoral Dissertation, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/13152.

MLA Handbook (7th Edition):

Verschoor, Meghan L. “The Role of the Transcription Factor Ets-1 in Mitochondrial Metabolism and Oxidative Stress.” 2013. Web. 18 Jan 2021.

Vancouver:

Verschoor ML. The Role of the Transcription Factor Ets-1 in Mitochondrial Metabolism and Oxidative Stress. [Internet] [Doctoral dissertation]. McMaster University; 2013. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/13152.

Council of Science Editors:

Verschoor ML. The Role of the Transcription Factor Ets-1 in Mitochondrial Metabolism and Oxidative Stress. [Doctoral Dissertation]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13152


McMaster University

19. DoHarris, Lindsay E. Effects of Extreme Temperature on Airway Smooth Muscle Cell Death.

Degree: MSc, 2011, McMaster University

Bronchial thermoplasty has recently been FDA approved as a novel therapy for use on adults suffering from severe asthma. The procedure uses radiofrequency energy… (more)

Subjects/Keywords: Asthma; Airway Smooth Muscle; Bronchial Thermoplasty; Heat; Cell Death; Medical Molecular Biology; Medical Molecular Biology

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

APA (6th Edition):

DoHarris, L. E. (2011). Effects of Extreme Temperature on Airway Smooth Muscle Cell Death. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11688

Chicago Manual of Style (16th Edition):

DoHarris, Lindsay E. “Effects of Extreme Temperature on Airway Smooth Muscle Cell Death.” 2011. Masters Thesis, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/11688.

MLA Handbook (7th Edition):

DoHarris, Lindsay E. “Effects of Extreme Temperature on Airway Smooth Muscle Cell Death.” 2011. Web. 18 Jan 2021.

Vancouver:

DoHarris LE. Effects of Extreme Temperature on Airway Smooth Muscle Cell Death. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/11688.

Council of Science Editors:

DoHarris LE. Effects of Extreme Temperature on Airway Smooth Muscle Cell Death. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11688


McMaster University

20. Storozhuk, Yaryna. MOLECULAR RESPONSES OF LUNG CANCER TO IONIZING RADIATION: INVESTIGATION OF THE BIGUANIDE METFORMIN IN COMBINATION WITH IONIZING RADIATION.

Degree: MSc, 2012, McMaster University

Purpose To examine the potential of the anti-diabetic agent Metformin (MET) to enhance responses of NSCLC to ionizing radiation (IR). Experimental Design Human NSCLC… (more)

Subjects/Keywords: AMPK; cancer; ionizing radiation; radiosensitizer; metformin; lung cancer; Medical Molecular Biology; Medical Molecular Biology

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

APA (6th Edition):

Storozhuk, Y. (2012). MOLECULAR RESPONSES OF LUNG CANCER TO IONIZING RADIATION: INVESTIGATION OF THE BIGUANIDE METFORMIN IN COMBINATION WITH IONIZING RADIATION. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12577

Chicago Manual of Style (16th Edition):

Storozhuk, Yaryna. “MOLECULAR RESPONSES OF LUNG CANCER TO IONIZING RADIATION: INVESTIGATION OF THE BIGUANIDE METFORMIN IN COMBINATION WITH IONIZING RADIATION.” 2012. Masters Thesis, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/12577.

MLA Handbook (7th Edition):

Storozhuk, Yaryna. “MOLECULAR RESPONSES OF LUNG CANCER TO IONIZING RADIATION: INVESTIGATION OF THE BIGUANIDE METFORMIN IN COMBINATION WITH IONIZING RADIATION.” 2012. Web. 18 Jan 2021.

Vancouver:

Storozhuk Y. MOLECULAR RESPONSES OF LUNG CANCER TO IONIZING RADIATION: INVESTIGATION OF THE BIGUANIDE METFORMIN IN COMBINATION WITH IONIZING RADIATION. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/12577.

Council of Science Editors:

Storozhuk Y. MOLECULAR RESPONSES OF LUNG CANCER TO IONIZING RADIATION: INVESTIGATION OF THE BIGUANIDE METFORMIN IN COMBINATION WITH IONIZING RADIATION. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12577


McMaster University

21. Wang, David Yu Chang. Regulation of macrophage SR-BI by lipoproteins and inflammatory stimuli.

Degree: MSc, 2011, McMaster University

In atherosclerotic plaques, macrophages ingest modified LDL and turn to foam cells. Others have shown that SR-BI expression levels inversely correlated with cellular cholesterol… (more)

Subjects/Keywords: Atherosclerosis receptor cholesterol inflammation macrophage lipoprotein; Biochemistry; Biology; Cell Biology; Immunity; Medical Biochemistry; Medical Cell Biology; Medical Molecular Biology; Medical Sciences; Molecular Biology; Biochemistry

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APA (6th Edition):

Wang, D. Y. C. (2011). Regulation of macrophage SR-BI by lipoproteins and inflammatory stimuli. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11219

Chicago Manual of Style (16th Edition):

Wang, David Yu Chang. “Regulation of macrophage SR-BI by lipoproteins and inflammatory stimuli.” 2011. Masters Thesis, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/11219.

MLA Handbook (7th Edition):

Wang, David Yu Chang. “Regulation of macrophage SR-BI by lipoproteins and inflammatory stimuli.” 2011. Web. 18 Jan 2021.

Vancouver:

Wang DYC. Regulation of macrophage SR-BI by lipoproteins and inflammatory stimuli. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/11219.

Council of Science Editors:

Wang DYC. Regulation of macrophage SR-BI by lipoproteins and inflammatory stimuli. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11219


University of Louisville

22. Sharpe, Jessica Mezzanotte. The discovery of a novel, Ras-mediated NORE1A/PMLIV tumor suppressor complex.

Degree: PhD, 2016, University of Louisville

  Ras is the most commonly activated oncogene in human cancer. Activated Ras drives cell growth and proliferation by activating multiple mitogenic signaling pathways. However,… (more)

Subjects/Keywords: Ras; NORE1A; PML; cancer; tumor suppressor; Medical Biochemistry; Medical Molecular Biology

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

APA (6th Edition):

Sharpe, J. M. (2016). The discovery of a novel, Ras-mediated NORE1A/PMLIV tumor suppressor complex. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/2539 ; https://ir.library.louisville.edu/etd/2539

Chicago Manual of Style (16th Edition):

Sharpe, Jessica Mezzanotte. “The discovery of a novel, Ras-mediated NORE1A/PMLIV tumor suppressor complex.” 2016. Doctoral Dissertation, University of Louisville. Accessed January 18, 2021. 10.18297/etd/2539 ; https://ir.library.louisville.edu/etd/2539.

MLA Handbook (7th Edition):

Sharpe, Jessica Mezzanotte. “The discovery of a novel, Ras-mediated NORE1A/PMLIV tumor suppressor complex.” 2016. Web. 18 Jan 2021.

Vancouver:

Sharpe JM. The discovery of a novel, Ras-mediated NORE1A/PMLIV tumor suppressor complex. [Internet] [Doctoral dissertation]. University of Louisville; 2016. [cited 2021 Jan 18]. Available from: 10.18297/etd/2539 ; https://ir.library.louisville.edu/etd/2539.

Council of Science Editors:

Sharpe JM. The discovery of a novel, Ras-mediated NORE1A/PMLIV tumor suppressor complex. [Doctoral Dissertation]. University of Louisville; 2016. Available from: 10.18297/etd/2539 ; https://ir.library.louisville.edu/etd/2539


University of Kentucky

23. Barnard, Sandra H. Amalgamation of Nucleosides and Amino Acids in Antibiotic Biosynthesis.

Degree: 2013, University of Kentucky

 The rapid increase in antibiotic resistance demands the identification of novel antibiotics with novel targets. One potential antibacterial target is the biosynthesis of peptidoglycan cell… (more)

Subjects/Keywords: L-Threonine Transaldolase; C-C Bond; Caprazamycin; Capuramycin; Serine Hydroxymethyltransferase; Biochemistry; Medical Biochemistry; Medical Cell Biology; Medical Education; Medical Microbiology; Medical Molecular Biology; Medicinal-Pharmaceutical Chemistry; Molecular Biology; Organic Chemistry

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APA (6th Edition):

Barnard, S. H. (2013). Amalgamation of Nucleosides and Amino Acids in Antibiotic Biosynthesis. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/20

Chicago Manual of Style (16th Edition):

Barnard, Sandra H. “Amalgamation of Nucleosides and Amino Acids in Antibiotic Biosynthesis.” 2013. Doctoral Dissertation, University of Kentucky. Accessed January 18, 2021. https://uknowledge.uky.edu/pharmacy_etds/20.

MLA Handbook (7th Edition):

Barnard, Sandra H. “Amalgamation of Nucleosides and Amino Acids in Antibiotic Biosynthesis.” 2013. Web. 18 Jan 2021.

Vancouver:

Barnard SH. Amalgamation of Nucleosides and Amino Acids in Antibiotic Biosynthesis. [Internet] [Doctoral dissertation]. University of Kentucky; 2013. [cited 2021 Jan 18]. Available from: https://uknowledge.uky.edu/pharmacy_etds/20.

Council of Science Editors:

Barnard SH. Amalgamation of Nucleosides and Amino Acids in Antibiotic Biosynthesis. [Doctoral Dissertation]. University of Kentucky; 2013. Available from: https://uknowledge.uky.edu/pharmacy_etds/20


University of Oxford

24. Malinauskas, Tomas. Structural and functional studies of Wnt signalling pathway antagonists.

Degree: PhD, 2011, University of Oxford

 Wnt morphogens control embryonic development and adult tissue homeostasis. Deregulation of the Wnt signalling pathway leads to human diseases. This thesis covers work on two… (more)

Subjects/Keywords: 572.6; Biochemistry; Biology (medical sciences); Molecular biophysics (biochemistry); Oncology; Biology

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APA (6th Edition):

Malinauskas, T. (2011). Structural and functional studies of Wnt signalling pathway antagonists. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:a3b71f18-9b90-408a-a5b5-2611e4ae2102 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558451

Chicago Manual of Style (16th Edition):

Malinauskas, Tomas. “Structural and functional studies of Wnt signalling pathway antagonists.” 2011. Doctoral Dissertation, University of Oxford. Accessed January 18, 2021. http://ora.ox.ac.uk/objects/uuid:a3b71f18-9b90-408a-a5b5-2611e4ae2102 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558451.

MLA Handbook (7th Edition):

Malinauskas, Tomas. “Structural and functional studies of Wnt signalling pathway antagonists.” 2011. Web. 18 Jan 2021.

Vancouver:

Malinauskas T. Structural and functional studies of Wnt signalling pathway antagonists. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2021 Jan 18]. Available from: http://ora.ox.ac.uk/objects/uuid:a3b71f18-9b90-408a-a5b5-2611e4ae2102 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558451.

Council of Science Editors:

Malinauskas T. Structural and functional studies of Wnt signalling pathway antagonists. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:a3b71f18-9b90-408a-a5b5-2611e4ae2102 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558451


University of Arkansas

25. Qassab, Abdullah. The First In Vivo Human Methionine Sulfide Proteome and the Impact of Smoking.

Degree: PhD, 2018, University of Arkansas

  Reactive oxygen species are naturally generated within the human body and they are known to modulate signaling pathway and mediate other physiological activities. However,… (more)

Subjects/Keywords: Mass spectrometry; Proteome; Smoker; Biochemistry; Macromolecular Substances; Medical Molecular Biology; Molecular Biology

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APA (6th Edition):

Qassab, A. (2018). The First In Vivo Human Methionine Sulfide Proteome and the Impact of Smoking. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/3105

Chicago Manual of Style (16th Edition):

Qassab, Abdullah. “The First In Vivo Human Methionine Sulfide Proteome and the Impact of Smoking.” 2018. Doctoral Dissertation, University of Arkansas. Accessed January 18, 2021. https://scholarworks.uark.edu/etd/3105.

MLA Handbook (7th Edition):

Qassab, Abdullah. “The First In Vivo Human Methionine Sulfide Proteome and the Impact of Smoking.” 2018. Web. 18 Jan 2021.

Vancouver:

Qassab A. The First In Vivo Human Methionine Sulfide Proteome and the Impact of Smoking. [Internet] [Doctoral dissertation]. University of Arkansas; 2018. [cited 2021 Jan 18]. Available from: https://scholarworks.uark.edu/etd/3105.

Council of Science Editors:

Qassab A. The First In Vivo Human Methionine Sulfide Proteome and the Impact of Smoking. [Doctoral Dissertation]. University of Arkansas; 2018. Available from: https://scholarworks.uark.edu/etd/3105


University of South Florida

26. Nelson, Nadine D. Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer.

Degree: 2015, University of South Florida

 Pancreatic cancer is one of the deadliest cancers with a five-year survival rate of 6%. Pancreatic cancer is resistant to conventional chemotherapy and is usually… (more)

Subjects/Keywords: Transcription Factor; CK2; PP1; Ubiquitination; Apigenin; Cell Biology; Medical Molecular Biology; Medical Sciences

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APA (6th Edition):

Nelson, N. D. (2015). Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5810

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):

Nelson, Nadine D. “Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer.” 2015. Thesis, University of South Florida. Accessed January 18, 2021. https://scholarcommons.usf.edu/etd/5810.

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

MLA Handbook (7th Edition):

Nelson, Nadine D. “Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer.” 2015. Web. 18 Jan 2021.

Vancouver:

Nelson ND. Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer. [Internet] [Thesis]. University of South Florida; 2015. [cited 2021 Jan 18]. Available from: https://scholarcommons.usf.edu/etd/5810.

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

Council of Science Editors:

Nelson ND. Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5810

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


University of Arkansas

27. Alismail, Hanan Abdulaziz. Enhanced Pancreatic beta-cells Proliferation and Functionality.

Degree: MS, 2013, University of Arkansas

  Biologically functional beta-cells proliferate at an extremely low rate with limited turnover capacity. This cellular property hinders cell-based therapy for clinical applications. Many attempts… (more)

Subjects/Keywords: Biological sciences; Cells; niche; pancreas; proliferation; Medical Cell Biology; Medical Molecular Biology

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APA (6th Edition):

Alismail, H. A. (2013). Enhanced Pancreatic beta-cells Proliferation and Functionality. (Masters Thesis). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/955

Chicago Manual of Style (16th Edition):

Alismail, Hanan Abdulaziz. “Enhanced Pancreatic beta-cells Proliferation and Functionality.” 2013. Masters Thesis, University of Arkansas. Accessed January 18, 2021. https://scholarworks.uark.edu/etd/955.

MLA Handbook (7th Edition):

Alismail, Hanan Abdulaziz. “Enhanced Pancreatic beta-cells Proliferation and Functionality.” 2013. Web. 18 Jan 2021.

Vancouver:

Alismail HA. Enhanced Pancreatic beta-cells Proliferation and Functionality. [Internet] [Masters thesis]. University of Arkansas; 2013. [cited 2021 Jan 18]. Available from: https://scholarworks.uark.edu/etd/955.

Council of Science Editors:

Alismail HA. Enhanced Pancreatic beta-cells Proliferation and Functionality. [Masters Thesis]. University of Arkansas; 2013. Available from: https://scholarworks.uark.edu/etd/955


McMaster University

28. Caron, Nicholas S. Using Förster Resonance Energy Transfer (FRET) To Define the Conformational Changes of Huntingtin at the Clinical Threshold for Huntington’s Disease.

Degree: PhD, 2014, McMaster University

Huntington’s disease (HD) is a progressive, neurodegenerative disorder that leads to the selective loss of neurons in the striatum and the cerebral cortex. HD… (more)

Subjects/Keywords: Huntington's disease; huntingtin; biosensor; FRET; Medical Cell Biology; Medical Molecular Biology; Nervous System Diseases; Medical Cell Biology

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APA (6th Edition):

Caron, N. S. (2014). Using Förster Resonance Energy Transfer (FRET) To Define the Conformational Changes of Huntingtin at the Clinical Threshold for Huntington’s Disease. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/15344

Chicago Manual of Style (16th Edition):

Caron, Nicholas S. “Using Förster Resonance Energy Transfer (FRET) To Define the Conformational Changes of Huntingtin at the Clinical Threshold for Huntington’s Disease.” 2014. Doctoral Dissertation, McMaster University. Accessed January 18, 2021. http://hdl.handle.net/11375/15344.

MLA Handbook (7th Edition):

Caron, Nicholas S. “Using Förster Resonance Energy Transfer (FRET) To Define the Conformational Changes of Huntingtin at the Clinical Threshold for Huntington’s Disease.” 2014. Web. 18 Jan 2021.

Vancouver:

Caron NS. Using Förster Resonance Energy Transfer (FRET) To Define the Conformational Changes of Huntingtin at the Clinical Threshold for Huntington’s Disease. [Internet] [Doctoral dissertation]. McMaster University; 2014. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11375/15344.

Council of Science Editors:

Caron NS. Using Förster Resonance Energy Transfer (FRET) To Define the Conformational Changes of Huntingtin at the Clinical Threshold for Huntington’s Disease. [Doctoral Dissertation]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/15344

29. Patters, Benjamin J. The Role of Exosomal Transport of Viral Agents in Persistent HIV Pathogenesis.

Degree: MS, Biomedical Sciences, 2018, University of Tennessee Health Science Center

  Human immunodeficiency virus (HIV) infection, despite great advances in antiretroviral therapy (ART), remains a lifelong affliction. Though current treatment regimens can effectively suppress viral… (more)

Subjects/Keywords: Exosome; HIV; Medical Biochemistry; Medical Molecular Biology; Medical Sciences; Medicine and Health Sciences

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APA (6th Edition):

Patters, B. J. (2018). The Role of Exosomal Transport of Viral Agents in Persistent HIV Pathogenesis. (Thesis). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/475

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):

Patters, Benjamin J. “The Role of Exosomal Transport of Viral Agents in Persistent HIV Pathogenesis.” 2018. Thesis, University of Tennessee Health Science Center. Accessed January 18, 2021. https://dc.uthsc.edu/dissertations/475.

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

MLA Handbook (7th Edition):

Patters, Benjamin J. “The Role of Exosomal Transport of Viral Agents in Persistent HIV Pathogenesis.” 2018. Web. 18 Jan 2021.

Vancouver:

Patters BJ. The Role of Exosomal Transport of Viral Agents in Persistent HIV Pathogenesis. [Internet] [Thesis]. University of Tennessee Health Science Center; 2018. [cited 2021 Jan 18]. Available from: https://dc.uthsc.edu/dissertations/475.

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

Council of Science Editors:

Patters BJ. The Role of Exosomal Transport of Viral Agents in Persistent HIV Pathogenesis. [Thesis]. University of Tennessee Health Science Center; 2018. Available from: https://dc.uthsc.edu/dissertations/475

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


East Tennessee State University

30. Hilton, Benjamin A. Investigation of Novel Functions for DNA Damage Response and Repair Proteins in Escherichia coli and Humans.

Degree: PhD, Biomedical Sciences, 2016, East Tennessee State University

  Endogenous and exogenous agents that can damage DNA are a constant threat to genome stability in all living cells. In response, cells have evolved… (more)

Subjects/Keywords: Nucleotide Excision Repair; UvrABC; XPC; XPA; ATR; Apoptosis; Biochemistry; Cancer Biology; Cell Biology; Medical Biochemistry; Medical Cell Biology; Molecular Biology

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APA (6th Edition):

Hilton, B. A. (2016). Investigation of Novel Functions for DNA Damage Response and Repair Proteins in Escherichia coli and Humans. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/3040

Chicago Manual of Style (16th Edition):

Hilton, Benjamin A. “Investigation of Novel Functions for DNA Damage Response and Repair Proteins in Escherichia coli and Humans.” 2016. Doctoral Dissertation, East Tennessee State University. Accessed January 18, 2021. https://dc.etsu.edu/etd/3040.

MLA Handbook (7th Edition):

Hilton, Benjamin A. “Investigation of Novel Functions for DNA Damage Response and Repair Proteins in Escherichia coli and Humans.” 2016. Web. 18 Jan 2021.

Vancouver:

Hilton BA. Investigation of Novel Functions for DNA Damage Response and Repair Proteins in Escherichia coli and Humans. [Internet] [Doctoral dissertation]. East Tennessee State University; 2016. [cited 2021 Jan 18]. Available from: https://dc.etsu.edu/etd/3040.

Council of Science Editors:

Hilton BA. Investigation of Novel Functions for DNA Damage Response and Repair Proteins in Escherichia coli and Humans. [Doctoral Dissertation]. East Tennessee State University; 2016. Available from: https://dc.etsu.edu/etd/3040

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