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You searched for +publisher:"McMaster University" +contributor:("Biochemistry"). Showing records 1 – 30 of 347 total matches.

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McMaster University

1. Bhatia, Sonam. TRANSCRIPTIONAL REGULATION OF PLURIPOTENCY AND CELL FATE.

Degree: PhD, 2017, McMaster University

Embryonic stem cells are pluripotent in nature, in that they can self-renew indefinitely, while maintaining the capability to give rise to all adult cell types.… (more)

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APA (6th Edition):

Bhatia, S. (2017). TRANSCRIPTIONAL REGULATION OF PLURIPOTENCY AND CELL FATE. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22035

Chicago Manual of Style (16th Edition):

Bhatia, Sonam. “TRANSCRIPTIONAL REGULATION OF PLURIPOTENCY AND CELL FATE.” 2017. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/22035.

MLA Handbook (7th Edition):

Bhatia, Sonam. “TRANSCRIPTIONAL REGULATION OF PLURIPOTENCY AND CELL FATE.” 2017. Web. 23 Feb 2020.

Vancouver:

Bhatia S. TRANSCRIPTIONAL REGULATION OF PLURIPOTENCY AND CELL FATE. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/22035.

Council of Science Editors:

Bhatia S. TRANSCRIPTIONAL REGULATION OF PLURIPOTENCY AND CELL FATE. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22035

2. Aslostovar, Lili. DOPAMINE RECEPTOR TARGETING IN HUMAN ACUTE MYELOID LEUKEMIA.

Degree: PhD, 2017, McMaster University

Standard of care chemotherapy for acute myeloid leukemia (AML) has remained unchanged for decades and is associated with therapy failure and unsatisfactory survival rates. While… (more)

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APA (6th Edition):

Aslostovar, L. (2017). DOPAMINE RECEPTOR TARGETING IN HUMAN ACUTE MYELOID LEUKEMIA. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22031

Chicago Manual of Style (16th Edition):

Aslostovar, Lili. “DOPAMINE RECEPTOR TARGETING IN HUMAN ACUTE MYELOID LEUKEMIA.” 2017. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/22031.

MLA Handbook (7th Edition):

Aslostovar, Lili. “DOPAMINE RECEPTOR TARGETING IN HUMAN ACUTE MYELOID LEUKEMIA.” 2017. Web. 23 Feb 2020.

Vancouver:

Aslostovar L. DOPAMINE RECEPTOR TARGETING IN HUMAN ACUTE MYELOID LEUKEMIA. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/22031.

Council of Science Editors:

Aslostovar L. DOPAMINE RECEPTOR TARGETING IN HUMAN ACUTE MYELOID LEUKEMIA. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22031


McMaster University

3. Lau, Jennifer T. Characterizing the diversity and complexity of the human gut microbiome through the combination of culture and culture-independent methods.

Degree: PhD, 2017, McMaster University

The human gut microbiome is the collection of all organisms and their genetic content that inhabit the gastrointestinal tract. An overwhelming number of studies have… (more)

Subjects/Keywords: gut microbiome; culture

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APA (6th Edition):

Lau, J. T. (2017). Characterizing the diversity and complexity of the human gut microbiome through the combination of culture and culture-independent methods. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22053

Chicago Manual of Style (16th Edition):

Lau, Jennifer T. “Characterizing the diversity and complexity of the human gut microbiome through the combination of culture and culture-independent methods.” 2017. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/22053.

MLA Handbook (7th Edition):

Lau, Jennifer T. “Characterizing the diversity and complexity of the human gut microbiome through the combination of culture and culture-independent methods.” 2017. Web. 23 Feb 2020.

Vancouver:

Lau JT. Characterizing the diversity and complexity of the human gut microbiome through the combination of culture and culture-independent methods. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/22053.

Council of Science Editors:

Lau JT. Characterizing the diversity and complexity of the human gut microbiome through the combination of culture and culture-independent methods. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22053


McMaster University

4. Jennings, William. A Structural and Enzymatic Characterization of Purified Human Diacylglycerol Kinase Epsilon.

Degree: MSc, 2016, McMaster University

Diacylglycerol kinases (DGK’s) tightly regulate the intracellular levels of diacylglycerol (DAG) and phosphatidic acid (PA). DAG is an important intermediate in lipid biosynthetic pathways and… (more)

Subjects/Keywords: Membrane Protein Biochemistry

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APA (6th Edition):

Jennings, W. (2016). A Structural and Enzymatic Characterization of Purified Human Diacylglycerol Kinase Epsilon. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/20488

Chicago Manual of Style (16th Edition):

Jennings, William. “A Structural and Enzymatic Characterization of Purified Human Diacylglycerol Kinase Epsilon.” 2016. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/20488.

MLA Handbook (7th Edition):

Jennings, William. “A Structural and Enzymatic Characterization of Purified Human Diacylglycerol Kinase Epsilon.” 2016. Web. 23 Feb 2020.

Vancouver:

Jennings W. A Structural and Enzymatic Characterization of Purified Human Diacylglycerol Kinase Epsilon. [Internet] [Masters thesis]. McMaster University; 2016. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/20488.

Council of Science Editors:

Jennings W. A Structural and Enzymatic Characterization of Purified Human Diacylglycerol Kinase Epsilon. [Masters Thesis]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20488


McMaster University

5. Holzapfel, Nicholas. Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia.

Degree: PhD, 2016, McMaster University

Musashi-2 (MSI2), a member of the Musashi family of RNA-binding proteins, is thought to play a critical role in the maintenance of stem cell populations… (more)

Subjects/Keywords: RNA-Binding Protein; Musashi; Hematopoiesis

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APA (6th Edition):

Holzapfel, N. (2016). Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/20628

Chicago Manual of Style (16th Edition):

Holzapfel, Nicholas. “Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia.” 2016. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/20628.

MLA Handbook (7th Edition):

Holzapfel, Nicholas. “Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia.” 2016. Web. 23 Feb 2020.

Vancouver:

Holzapfel N. Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia. [Internet] [Doctoral dissertation]. McMaster University; 2016. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/20628.

Council of Science Editors:

Holzapfel N. Investigating the Role of the RNA-Binding Protein MUSASHI-2 (MSI2) in Normal Hematopoiesis and Leukemia. [Doctoral Dissertation]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20628


McMaster University

6. Mendonca, Michelle L. Characterizing Cooperative and competitive interactions involving Streptococcus intermedius.

Degree: PhD, 2017, McMaster University

 The Streptococcus Anginosus/Milleri group (SMG) colonize mucosal surfaces in humans but are also associated with numerous respiratory and invasive infections. These infections are often polymicrobial… (more)

Subjects/Keywords: Streptococcus intermedius; polymicrobial interactions

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APA (6th Edition):

Mendonca, M. L. (2017). Characterizing Cooperative and competitive interactions involving Streptococcus intermedius. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/20968

Chicago Manual of Style (16th Edition):

Mendonca, Michelle L. “Characterizing Cooperative and competitive interactions involving Streptococcus intermedius.” 2017. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/20968.

MLA Handbook (7th Edition):

Mendonca, Michelle L. “Characterizing Cooperative and competitive interactions involving Streptococcus intermedius.” 2017. Web. 23 Feb 2020.

Vancouver:

Mendonca ML. Characterizing Cooperative and competitive interactions involving Streptococcus intermedius. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/20968.

Council of Science Editors:

Mendonca ML. Characterizing Cooperative and competitive interactions involving Streptococcus intermedius. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/20968


McMaster University

7. Tuinema, Brian. Innate Immunity Evasion Through D-Amino Acid Sequestration.

Degree: PhD, 2017, McMaster University

The innate immune system functions to limit the spread of bacteria during an infection. This is achieved through a highly complex assault on infiltrating pathogens.… (more)

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APA (6th Edition):

Tuinema, B. (2017). Innate Immunity Evasion Through D-Amino Acid Sequestration. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/21985

Chicago Manual of Style (16th Edition):

Tuinema, Brian. “Innate Immunity Evasion Through D-Amino Acid Sequestration.” 2017. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/21985.

MLA Handbook (7th Edition):

Tuinema, Brian. “Innate Immunity Evasion Through D-Amino Acid Sequestration.” 2017. Web. 23 Feb 2020.

Vancouver:

Tuinema B. Innate Immunity Evasion Through D-Amino Acid Sequestration. [Internet] [Doctoral dissertation]. McMaster University; 2017. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/21985.

Council of Science Editors:

Tuinema B. Innate Immunity Evasion Through D-Amino Acid Sequestration. [Doctoral Dissertation]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/21985


McMaster University

8. Garden, Daniel. THEORETICAL STUDY OF STATE-DEPENDENT ACTION OF TOXINS AND DRUGS IN A VOLTAGE GATED SODIUM CHANNEL.

Degree: PhD, 2011, McMaster University

  Ion permeation through voltage gated sodium channels is modulated by many drugs and toxins. However, the atomistic mechanisms of action of most these ligands… (more)

Subjects/Keywords: Ion Channels; Molecular Modeling; Drug Docking; Monte Carlo Minimization; Biochemistry; Biophysics; Biotechnology; Structural Biology; Biochemistry

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APA (6th Edition):

Garden, D. (2011). THEORETICAL STUDY OF STATE-DEPENDENT ACTION OF TOXINS AND DRUGS IN A VOLTAGE GATED SODIUM CHANNEL. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/10083

Chicago Manual of Style (16th Edition):

Garden, Daniel. “THEORETICAL STUDY OF STATE-DEPENDENT ACTION OF TOXINS AND DRUGS IN A VOLTAGE GATED SODIUM CHANNEL.” 2011. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/10083.

MLA Handbook (7th Edition):

Garden, Daniel. “THEORETICAL STUDY OF STATE-DEPENDENT ACTION OF TOXINS AND DRUGS IN A VOLTAGE GATED SODIUM CHANNEL.” 2011. Web. 23 Feb 2020.

Vancouver:

Garden D. THEORETICAL STUDY OF STATE-DEPENDENT ACTION OF TOXINS AND DRUGS IN A VOLTAGE GATED SODIUM CHANNEL. [Internet] [Doctoral dissertation]. McMaster University; 2011. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/10083.

Council of Science Editors:

Garden D. THEORETICAL STUDY OF STATE-DEPENDENT ACTION OF TOXINS AND DRUGS IN A VOLTAGE GATED SODIUM CHANNEL. [Doctoral Dissertation]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/10083


McMaster University

9. HENDERSON, SARA. EXAMINING ZINC RELEASE FROM PLATELETS AND ITS MODULATION OF CLOT STRUCTURE AND FIBRINOLYSIS.

Degree: PhD, 2016, McMaster University

Zinc (Zn2+) is an abundant metal ion that circulates in the body. Within hemostasis, Zn2+ participates in platelet aggregation, coagulation, and fibrinolysis. At the site… (more)

Subjects/Keywords: ZINC; COAGULATION; FIBRINOLYSIS; PLATELETS

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APA (6th Edition):

HENDERSON, S. (2016). EXAMINING ZINC RELEASE FROM PLATELETS AND ITS MODULATION OF CLOT STRUCTURE AND FIBRINOLYSIS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/18684

Chicago Manual of Style (16th Edition):

HENDERSON, SARA. “EXAMINING ZINC RELEASE FROM PLATELETS AND ITS MODULATION OF CLOT STRUCTURE AND FIBRINOLYSIS.” 2016. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/18684.

MLA Handbook (7th Edition):

HENDERSON, SARA. “EXAMINING ZINC RELEASE FROM PLATELETS AND ITS MODULATION OF CLOT STRUCTURE AND FIBRINOLYSIS.” 2016. Web. 23 Feb 2020.

Vancouver:

HENDERSON S. EXAMINING ZINC RELEASE FROM PLATELETS AND ITS MODULATION OF CLOT STRUCTURE AND FIBRINOLYSIS. [Internet] [Doctoral dissertation]. McMaster University; 2016. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/18684.

Council of Science Editors:

HENDERSON S. EXAMINING ZINC RELEASE FROM PLATELETS AND ITS MODULATION OF CLOT STRUCTURE AND FIBRINOLYSIS. [Doctoral Dissertation]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/18684


McMaster University

10. Yu, Pei. THE HIGH DENSITY LIPOPROTEIN AND ATHEROSCLEROSIS.

Degree: PhD, 2016, McMaster University

Coronary artery disease results from atherosclerotic plaque formation. High-density lipoprotein (HDL) has been shown to be inversely associated with the risk of coronary artery disease.… (more)

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APA (6th Edition):

Yu, P. (2016). THE HIGH DENSITY LIPOPROTEIN AND ATHEROSCLEROSIS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/18955

Chicago Manual of Style (16th Edition):

Yu, Pei. “THE HIGH DENSITY LIPOPROTEIN AND ATHEROSCLEROSIS.” 2016. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/18955.

MLA Handbook (7th Edition):

Yu, Pei. “THE HIGH DENSITY LIPOPROTEIN AND ATHEROSCLEROSIS.” 2016. Web. 23 Feb 2020.

Vancouver:

Yu P. THE HIGH DENSITY LIPOPROTEIN AND ATHEROSCLEROSIS. [Internet] [Doctoral dissertation]. McMaster University; 2016. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/18955.

Council of Science Editors:

Yu P. THE HIGH DENSITY LIPOPROTEIN AND ATHEROSCLEROSIS. [Doctoral Dissertation]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/18955


McMaster University

11. Adil Khan, Mohammed. Molecular Basis of Lipid Acyl Chain Selection by the Integral Outer Membrane Phospholipid:Lipid A Palmitoyltransferase PagP from Escherichia Coli.

Degree: PhD, 2010, McMaster University

The role of membrane-intrinsic enzymes of lipid metabolism in complex biological processes is being realized through comprehensive structure function studies. Detailed analysis of substrate-enzyme interactions… (more)

Subjects/Keywords: lipid metabolism; PagP; Escherichia coli; β-barrel; substrate recognition; substrate binding; acyl-chain; lipid diffusion

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APA (6th Edition):

Adil Khan, M. (2010). Molecular Basis of Lipid Acyl Chain Selection by the Integral Outer Membrane Phospholipid:Lipid A Palmitoyltransferase PagP from Escherichia Coli. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/19046

Chicago Manual of Style (16th Edition):

Adil Khan, Mohammed. “Molecular Basis of Lipid Acyl Chain Selection by the Integral Outer Membrane Phospholipid:Lipid A Palmitoyltransferase PagP from Escherichia Coli.” 2010. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/19046.

MLA Handbook (7th Edition):

Adil Khan, Mohammed. “Molecular Basis of Lipid Acyl Chain Selection by the Integral Outer Membrane Phospholipid:Lipid A Palmitoyltransferase PagP from Escherichia Coli.” 2010. Web. 23 Feb 2020.

Vancouver:

Adil Khan M. Molecular Basis of Lipid Acyl Chain Selection by the Integral Outer Membrane Phospholipid:Lipid A Palmitoyltransferase PagP from Escherichia Coli. [Internet] [Doctoral dissertation]. McMaster University; 2010. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/19046.

Council of Science Editors:

Adil Khan M. Molecular Basis of Lipid Acyl Chain Selection by the Integral Outer Membrane Phospholipid:Lipid A Palmitoyltransferase PagP from Escherichia Coli. [Doctoral Dissertation]. McMaster University; 2010. Available from: http://hdl.handle.net/11375/19046


McMaster University

12. Giltner, Carmen. Characterization of minor pilins in Pseudomonas aeruginosa.

Degree: PhD, 2010, McMaster University

Type II Secretion (T2S) and type IV pilus (T4P) systems in Gram-negative bacteria share many features that suggest a common ancestral origin. This study… (more)

Subjects/Keywords: minor pilins; Pseudomonas aeruginosa; Gram-negative bacteria; putative adhesin

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APA (6th Edition):

Giltner, C. (2010). Characterization of minor pilins in Pseudomonas aeruginosa. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/19455

Chicago Manual of Style (16th Edition):

Giltner, Carmen. “Characterization of minor pilins in Pseudomonas aeruginosa.” 2010. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/19455.

MLA Handbook (7th Edition):

Giltner, Carmen. “Characterization of minor pilins in Pseudomonas aeruginosa.” 2010. Web. 23 Feb 2020.

Vancouver:

Giltner C. Characterization of minor pilins in Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. McMaster University; 2010. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/19455.

Council of Science Editors:

Giltner C. Characterization of minor pilins in Pseudomonas aeruginosa. [Doctoral Dissertation]. McMaster University; 2010. Available from: http://hdl.handle.net/11375/19455


McMaster University

13. Rashid, Sabih. ENVIRONMENTAL FACTORS REGULATE DEVELOPMENTAL RATE IN C. ELEGANS.

Degree: MSc, 2018, McMaster University

Environmental factors, such as diet, can have a significant impact on the health of animals, influencing lifespan, development, and disease progression. The model organism Caenorhabditis… (more)

Subjects/Keywords: C. elegans; amino acids; TOR; developmental rate; bacteria

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APA (6th Edition):

Rashid, S. (2018). ENVIRONMENTAL FACTORS REGULATE DEVELOPMENTAL RATE IN C. ELEGANS. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/24156

Chicago Manual of Style (16th Edition):

Rashid, Sabih. “ENVIRONMENTAL FACTORS REGULATE DEVELOPMENTAL RATE IN C. ELEGANS.” 2018. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/24156.

MLA Handbook (7th Edition):

Rashid, Sabih. “ENVIRONMENTAL FACTORS REGULATE DEVELOPMENTAL RATE IN C. ELEGANS.” 2018. Web. 23 Feb 2020.

Vancouver:

Rashid S. ENVIRONMENTAL FACTORS REGULATE DEVELOPMENTAL RATE IN C. ELEGANS. [Internet] [Masters thesis]. McMaster University; 2018. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/24156.

Council of Science Editors:

Rashid S. ENVIRONMENTAL FACTORS REGULATE DEVELOPMENTAL RATE IN C. ELEGANS. [Masters Thesis]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/24156


McMaster University

14. Wong, Jessica. Characterizing the Stability and Mechanism of Human Mismatch Repair Factor MutLα.

Degree: MSc, 2011, McMaster University

DNA mismatch repair (MMR) is a highly conserved process that is responsible for maintaining genome stability where its main role is repairing replication errors… (more)

Subjects/Keywords: Biochemistry; Biochemistry

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APA (6th Edition):

Wong, J. (2011). Characterizing the Stability and Mechanism of Human Mismatch Repair Factor MutLα. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11135

Chicago Manual of Style (16th Edition):

Wong, Jessica. “Characterizing the Stability and Mechanism of Human Mismatch Repair Factor MutLα.” 2011. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/11135.

MLA Handbook (7th Edition):

Wong, Jessica. “Characterizing the Stability and Mechanism of Human Mismatch Repair Factor MutLα.” 2011. Web. 23 Feb 2020.

Vancouver:

Wong J. Characterizing the Stability and Mechanism of Human Mismatch Repair Factor MutLα. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/11135.

Council of Science Editors:

Wong J. Characterizing the Stability and Mechanism of Human Mismatch Repair Factor MutLα. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11135


McMaster University

15. Andres, Sara N. Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair.

Degree: PhD, 2011, McMaster University

DNA double-strand breaks pose a serious threat to genomic integrity. Double-strand breaks can cause chromosomal rearrangement, leading to uncontrolled cell proliferation, or even cell… (more)

Subjects/Keywords: XRCC4; XLF; Non-homologous end-joining; DNA repair; X-ray crystallography; Biochemistry, Biophysics, and Structural Biology; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

Andres, S. N. (2011). Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/11265

Chicago Manual of Style (16th Edition):

Andres, Sara N. “Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair.” 2011. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/11265.

MLA Handbook (7th Edition):

Andres, Sara N. “Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair.” 2011. Web. 23 Feb 2020.

Vancouver:

Andres SN. Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair. [Internet] [Doctoral dissertation]. McMaster University; 2011. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/11265.

Council of Science Editors:

Andres SN. Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair. [Doctoral Dissertation]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11265


McMaster University

16. Cooper, Colin. THE VIRULENCE CHAPERONE NETWORK ASSOCIATED WITH THE SPI-2 ENCODED TYPE THREE SECRETION SYSTEM OF SALMONELLA ENTERICA.

Degree: PhD, 2011, McMaster University

Bacteria employ virulence mechanisms to promote fitness that are generally detrimental to a host organism. The Gram-negative pathogen Salmonella enterica utilizes type three secretion… (more)

Subjects/Keywords: Salmonella; enterica; virulence; chaperone; T3SS; pathogen; effector; SPI-2; Bacteriology; Biochemistry; Molecular Biology; Other Biochemistry, Biophysics, and Structural Biology; Pathogenic Microbiology; Structural Biology; Bacteriology

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APA (6th Edition):

Cooper, C. (2011). THE VIRULENCE CHAPERONE NETWORK ASSOCIATED WITH THE SPI-2 ENCODED TYPE THREE SECRETION SYSTEM OF SALMONELLA ENTERICA. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/11641

Chicago Manual of Style (16th Edition):

Cooper, Colin. “THE VIRULENCE CHAPERONE NETWORK ASSOCIATED WITH THE SPI-2 ENCODED TYPE THREE SECRETION SYSTEM OF SALMONELLA ENTERICA.” 2011. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/11641.

MLA Handbook (7th Edition):

Cooper, Colin. “THE VIRULENCE CHAPERONE NETWORK ASSOCIATED WITH THE SPI-2 ENCODED TYPE THREE SECRETION SYSTEM OF SALMONELLA ENTERICA.” 2011. Web. 23 Feb 2020.

Vancouver:

Cooper C. THE VIRULENCE CHAPERONE NETWORK ASSOCIATED WITH THE SPI-2 ENCODED TYPE THREE SECRETION SYSTEM OF SALMONELLA ENTERICA. [Internet] [Doctoral dissertation]. McMaster University; 2011. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/11641.

Council of Science Editors:

Cooper C. THE VIRULENCE CHAPERONE NETWORK ASSOCIATED WITH THE SPI-2 ENCODED TYPE THREE SECRETION SYSTEM OF SALMONELLA ENTERICA. [Doctoral Dissertation]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11641


McMaster University

17. Campbell, JV Clinton. The Role of the In Vivo Microenvironment in Human Stem Cell Fate Decisions.

Degree: PhD, 2012, McMaster University

  Years of research in the field of stem cell biology have resulted in only modest gains in our ability to purify human stem cells… (more)

Subjects/Keywords: Stem cells; self-renewal; cancer; leukemia; niche; Cell Biology; Cell Biology

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APA (6th Edition):

Campbell, J. C. (2012). The Role of the In Vivo Microenvironment in Human Stem Cell Fate Decisions. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/11915

Chicago Manual of Style (16th Edition):

Campbell, JV Clinton. “The Role of the In Vivo Microenvironment in Human Stem Cell Fate Decisions.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/11915.

MLA Handbook (7th Edition):

Campbell, JV Clinton. “The Role of the In Vivo Microenvironment in Human Stem Cell Fate Decisions.” 2012. Web. 23 Feb 2020.

Vancouver:

Campbell JC. The Role of the In Vivo Microenvironment in Human Stem Cell Fate Decisions. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/11915.

Council of Science Editors:

Campbell JC. The Role of the In Vivo Microenvironment in Human Stem Cell Fate Decisions. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/11915


McMaster University

18. Lee, Jennifer A. TOWARDS THE DEVELOPMENT OF A CYTOCHROME C BIOSENSOR.

Degree: MSc, 2012, McMaster University

Cytochrome c (Cyt c) is a heme-containing protein that is a component of the electron transport chain as well as the mitochondrial apoptotic pathway.… (more)

Subjects/Keywords: Cytochrome c; aptazyme; biosensor; in vitro selection; Biochemistry; Laboratory and Basic Science Research; Biochemistry

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APA (6th Edition):

Lee, J. A. (2012). TOWARDS THE DEVELOPMENT OF A CYTOCHROME C BIOSENSOR. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11921

Chicago Manual of Style (16th Edition):

Lee, Jennifer A. “TOWARDS THE DEVELOPMENT OF A CYTOCHROME C BIOSENSOR.” 2012. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/11921.

MLA Handbook (7th Edition):

Lee, Jennifer A. “TOWARDS THE DEVELOPMENT OF A CYTOCHROME C BIOSENSOR.” 2012. Web. 23 Feb 2020.

Vancouver:

Lee JA. TOWARDS THE DEVELOPMENT OF A CYTOCHROME C BIOSENSOR. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/11921.

Council of Science Editors:

Lee JA. TOWARDS THE DEVELOPMENT OF A CYTOCHROME C BIOSENSOR. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/11921


McMaster University

19. Nolte, Sara M. THE DEVELOPMENT OF A MODEL SYSTEM FOR THE CHARACTERIZATION OF CANCER STEM CELL PROPERTIES IN BRAIN METASTASES FROM THE LUNG.

Degree: MSc, 2012, McMaster University

Brain metastases are most common in adults suffering from lung cancer, predicting uniformly poor patient outcome and short survival time. Despite their frequency and… (more)

Subjects/Keywords: brain metastasis; metastatic lung cancer; cancer stem cell; tumour-initiating cell; Cancer Biology; Cancer Biology

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APA (6th Edition):

Nolte, S. M. (2012). THE DEVELOPMENT OF A MODEL SYSTEM FOR THE CHARACTERIZATION OF CANCER STEM CELL PROPERTIES IN BRAIN METASTASES FROM THE LUNG. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12050

Chicago Manual of Style (16th Edition):

Nolte, Sara M. “THE DEVELOPMENT OF A MODEL SYSTEM FOR THE CHARACTERIZATION OF CANCER STEM CELL PROPERTIES IN BRAIN METASTASES FROM THE LUNG.” 2012. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12050.

MLA Handbook (7th Edition):

Nolte, Sara M. “THE DEVELOPMENT OF A MODEL SYSTEM FOR THE CHARACTERIZATION OF CANCER STEM CELL PROPERTIES IN BRAIN METASTASES FROM THE LUNG.” 2012. Web. 23 Feb 2020.

Vancouver:

Nolte SM. THE DEVELOPMENT OF A MODEL SYSTEM FOR THE CHARACTERIZATION OF CANCER STEM CELL PROPERTIES IN BRAIN METASTASES FROM THE LUNG. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12050.

Council of Science Editors:

Nolte SM. THE DEVELOPMENT OF A MODEL SYSTEM FOR THE CHARACTERIZATION OF CANCER STEM CELL PROPERTIES IN BRAIN METASTASES FROM THE LUNG. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12050


McMaster University

20. Shulga, Yulia V. Properties of Two Enzymes Involved in the Phosphoinositide Cycle – Diacylglycerol Kinase and Phosphatidylinositol 4-Phosphate 5-Kinase.

Degree: PhD, 2012, McMaster University

The two lipid kinases, diacylglycerol kinase (DGK) and phosphatidylinositol 4-phosphate 5-kinase (PIP5K), are vital players of the phosphatidylinositol cycle. DGK regulates the intracellular balance… (more)

Subjects/Keywords: phosphoinositide cycle; diacylglycerol kinase; acyl chain specificity; Biochemistry; Biochemistry

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APA (6th Edition):

Shulga, Y. V. (2012). Properties of Two Enzymes Involved in the Phosphoinositide Cycle – Diacylglycerol Kinase and Phosphatidylinositol 4-Phosphate 5-Kinase. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12077

Chicago Manual of Style (16th Edition):

Shulga, Yulia V. “Properties of Two Enzymes Involved in the Phosphoinositide Cycle – Diacylglycerol Kinase and Phosphatidylinositol 4-Phosphate 5-Kinase.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12077.

MLA Handbook (7th Edition):

Shulga, Yulia V. “Properties of Two Enzymes Involved in the Phosphoinositide Cycle – Diacylglycerol Kinase and Phosphatidylinositol 4-Phosphate 5-Kinase.” 2012. Web. 23 Feb 2020.

Vancouver:

Shulga YV. Properties of Two Enzymes Involved in the Phosphoinositide Cycle – Diacylglycerol Kinase and Phosphatidylinositol 4-Phosphate 5-Kinase. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12077.

Council of Science Editors:

Shulga YV. Properties of Two Enzymes Involved in the Phosphoinositide Cycle – Diacylglycerol Kinase and Phosphatidylinositol 4-Phosphate 5-Kinase. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12077


McMaster University

21. Takhar, Herlinder K. ROLE OF THE PSEUDOMONAS AERUGINOSA INNER MEMBRANE PROTEIN PILC IN TYPE IV PILUS FUNCTION.

Degree: MSc, 2012, McMaster University

Type 4 pili (T4P) are fibrous appendages found on the surfaces of a wide range of bacteria. They are used for adherence to biotic… (more)

Subjects/Keywords: Pseudomonas aeruginosa; Type IV pili; 2012; Herlinder; Takhar; Medicine and Health Sciences; Medicine and Health Sciences

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APA (6th Edition):

Takhar, H. K. (2012). ROLE OF THE PSEUDOMONAS AERUGINOSA INNER MEMBRANE PROTEIN PILC IN TYPE IV PILUS FUNCTION. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12092

Chicago Manual of Style (16th Edition):

Takhar, Herlinder K. “ROLE OF THE PSEUDOMONAS AERUGINOSA INNER MEMBRANE PROTEIN PILC IN TYPE IV PILUS FUNCTION.” 2012. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12092.

MLA Handbook (7th Edition):

Takhar, Herlinder K. “ROLE OF THE PSEUDOMONAS AERUGINOSA INNER MEMBRANE PROTEIN PILC IN TYPE IV PILUS FUNCTION.” 2012. Web. 23 Feb 2020.

Vancouver:

Takhar HK. ROLE OF THE PSEUDOMONAS AERUGINOSA INNER MEMBRANE PROTEIN PILC IN TYPE IV PILUS FUNCTION. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12092.

Council of Science Editors:

Takhar HK. ROLE OF THE PSEUDOMONAS AERUGINOSA INNER MEMBRANE PROTEIN PILC IN TYPE IV PILUS FUNCTION. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12092


McMaster University

22. Bharat, Amrita. The ribosomal function and GTPase activity of Escherichia coli EngA.

Degree: PhD, 2012, McMaster University

Ribosome biogenesis is a major metabolic expense of bacteria and a promising target for antibacterial drug discovery. Trans-acting proteins, called ribosome biogenesis factors, aid… (more)

Subjects/Keywords: ribosome biogenesis factor; chemical genetics; rRNA reporter; HTS; Der; YfgK; Biochemistry; Biochemistry

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APA (6th Edition):

Bharat, A. (2012). The ribosomal function and GTPase activity of Escherichia coli EngA. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12330

Chicago Manual of Style (16th Edition):

Bharat, Amrita. “The ribosomal function and GTPase activity of Escherichia coli EngA.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12330.

MLA Handbook (7th Edition):

Bharat, Amrita. “The ribosomal function and GTPase activity of Escherichia coli EngA.” 2012. Web. 23 Feb 2020.

Vancouver:

Bharat A. The ribosomal function and GTPase activity of Escherichia coli EngA. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12330.

Council of Science Editors:

Bharat A. The ribosomal function and GTPase activity of Escherichia coli EngA. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12330


McMaster University

23. Rodriguez, Linda. Direct Conversion of Fibroblasts to Hematopoietic Progenitors.

Degree: MSc, 2012, McMaster University

Immunodeficient-causing diseases such as HIV and leukemia have no cures, often require meticulous treatments and result in high morbidity or mortality. Although bone marrow… (more)

Subjects/Keywords: direct conversion; lymphopoiesis; hematopoietic progenitor; OCT4; Biochemistry, Biophysics, and Structural Biology; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

Rodriguez, L. (2012). Direct Conversion of Fibroblasts to Hematopoietic Progenitors. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12368

Chicago Manual of Style (16th Edition):

Rodriguez, Linda. “Direct Conversion of Fibroblasts to Hematopoietic Progenitors.” 2012. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12368.

MLA Handbook (7th Edition):

Rodriguez, Linda. “Direct Conversion of Fibroblasts to Hematopoietic Progenitors.” 2012. Web. 23 Feb 2020.

Vancouver:

Rodriguez L. Direct Conversion of Fibroblasts to Hematopoietic Progenitors. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12368.

Council of Science Editors:

Rodriguez L. Direct Conversion of Fibroblasts to Hematopoietic Progenitors. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12368


McMaster University

24. McManus, Simon A. CHARACTERIZATION AND APPLICATION OF SELF-PHOSPHORYLATING DEOXYRIBOZYMES.

Degree: PhD, 2012, McMaster University

The process of in vitro selection has led to the isolation of many catalytic DNA molecules, called deoxyribozymes, which can catalyze a range of… (more)

Subjects/Keywords: quadruplex; biosensor; DNAzyme; SELEX; Biochemistry, Biophysics, and Structural Biology; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

McManus, S. A. (2012). CHARACTERIZATION AND APPLICATION OF SELF-PHOSPHORYLATING DEOXYRIBOZYMES. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12405

Chicago Manual of Style (16th Edition):

McManus, Simon A. “CHARACTERIZATION AND APPLICATION OF SELF-PHOSPHORYLATING DEOXYRIBOZYMES.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12405.

MLA Handbook (7th Edition):

McManus, Simon A. “CHARACTERIZATION AND APPLICATION OF SELF-PHOSPHORYLATING DEOXYRIBOZYMES.” 2012. Web. 23 Feb 2020.

Vancouver:

McManus SA. CHARACTERIZATION AND APPLICATION OF SELF-PHOSPHORYLATING DEOXYRIBOZYMES. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12405.

Council of Science Editors:

McManus SA. CHARACTERIZATION AND APPLICATION OF SELF-PHOSPHORYLATING DEOXYRIBOZYMES. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12405


McMaster University

25. Osborne, Suzanne. Cis-Regulatory Evolution in Salmonella enterica.

Degree: PhD, 2012, McMaster University

Originally considered the sole providence of protein coding sequences, evolutionary biology has begun to recognize the importance of non-coding DNA in dictating phenotypic adaptation.… (more)

Subjects/Keywords: Salmonella; evolution; infection; Pathogenic Microbiology; Pathogenic Microbiology

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APA (6th Edition):

Osborne, S. (2012). Cis-Regulatory Evolution in Salmonella enterica. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12422

Chicago Manual of Style (16th Edition):

Osborne, Suzanne. “Cis-Regulatory Evolution in Salmonella enterica.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12422.

MLA Handbook (7th Edition):

Osborne, Suzanne. “Cis-Regulatory Evolution in Salmonella enterica.” 2012. Web. 23 Feb 2020.

Vancouver:

Osborne S. Cis-Regulatory Evolution in Salmonella enterica. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12422.

Council of Science Editors:

Osborne S. Cis-Regulatory Evolution in Salmonella enterica. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12422


McMaster University

26. Craney, Arryn. SMALL MOLECULE INTERROGATION OF S. COELICOLOR GROWTH, DEVELOPMENT AND SECONDARY METABOLISM.

Degree: PhD, 2012, McMaster University

Secondary metabolites are vital to human health and strategies to improve their production and detection are equally essential. The blue pigmented metabolite actinorhodin produced… (more)

Subjects/Keywords: streptomyces; secondary metabolism; small molecule screening; Biochemistry; Biochemistry

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APA (6th Edition):

Craney, A. (2012). SMALL MOLECULE INTERROGATION OF S. COELICOLOR GROWTH, DEVELOPMENT AND SECONDARY METABOLISM. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12453

Chicago Manual of Style (16th Edition):

Craney, Arryn. “SMALL MOLECULE INTERROGATION OF S. COELICOLOR GROWTH, DEVELOPMENT AND SECONDARY METABOLISM.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12453.

MLA Handbook (7th Edition):

Craney, Arryn. “SMALL MOLECULE INTERROGATION OF S. COELICOLOR GROWTH, DEVELOPMENT AND SECONDARY METABOLISM.” 2012. Web. 23 Feb 2020.

Vancouver:

Craney A. SMALL MOLECULE INTERROGATION OF S. COELICOLOR GROWTH, DEVELOPMENT AND SECONDARY METABOLISM. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12453.

Council of Science Editors:

Craney A. SMALL MOLECULE INTERROGATION OF S. COELICOLOR GROWTH, DEVELOPMENT AND SECONDARY METABOLISM. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12453


McMaster University

27. Hallett, Robin M. USING GENE EXPRESSION ANALYSIS TO GUIDE AND IDENTIFY TREATMENTS FOR BREAST CANCER PATIENTS.

Degree: PhD, 2012, McMaster University

Based on breast cancer clinical trial data accumulated over the last several decades it is obvious that standard breast cancer therapeutics extend survival in… (more)

Subjects/Keywords: Breast cancer; gene expression profiling; cancer stem cells; tumor-initating cells; biomarkers; Bioinformatics; Computational Biology; Genomics; Molecular Biology; Bioinformatics

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APA (6th Edition):

Hallett, R. M. (2012). USING GENE EXPRESSION ANALYSIS TO GUIDE AND IDENTIFY TREATMENTS FOR BREAST CANCER PATIENTS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12492

Chicago Manual of Style (16th Edition):

Hallett, Robin M. “USING GENE EXPRESSION ANALYSIS TO GUIDE AND IDENTIFY TREATMENTS FOR BREAST CANCER PATIENTS.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12492.

MLA Handbook (7th Edition):

Hallett, Robin M. “USING GENE EXPRESSION ANALYSIS TO GUIDE AND IDENTIFY TREATMENTS FOR BREAST CANCER PATIENTS.” 2012. Web. 23 Feb 2020.

Vancouver:

Hallett RM. USING GENE EXPRESSION ANALYSIS TO GUIDE AND IDENTIFY TREATMENTS FOR BREAST CANCER PATIENTS. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12492.

Council of Science Editors:

Hallett RM. USING GENE EXPRESSION ANALYSIS TO GUIDE AND IDENTIFY TREATMENTS FOR BREAST CANCER PATIENTS. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12492


McMaster University

28. Mok, Wendy (Wing Ki). DECODING TOXICITY: CHARACTERIZATION OF THE IBSC/SIBC TYPE I TOXIN-ANTITOXIN SYSTEM OF ESCHERICHIA COLI.

Degree: PhD, 2012, McMaster University

Small RNAs and small proteins encoded in diverse microbial genomes have been shown to play big parts in regulatory processes that are vital to… (more)

Subjects/Keywords: Biochemistry; Microbiology; Molecular Biology; Biochemistry

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APA (6th Edition):

Mok, W. (. K. (2012). DECODING TOXICITY: CHARACTERIZATION OF THE IBSC/SIBC TYPE I TOXIN-ANTITOXIN SYSTEM OF ESCHERICHIA COLI. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12530

Chicago Manual of Style (16th Edition):

Mok, Wendy (Wing Ki). “DECODING TOXICITY: CHARACTERIZATION OF THE IBSC/SIBC TYPE I TOXIN-ANTITOXIN SYSTEM OF ESCHERICHIA COLI.” 2012. Doctoral Dissertation, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12530.

MLA Handbook (7th Edition):

Mok, Wendy (Wing Ki). “DECODING TOXICITY: CHARACTERIZATION OF THE IBSC/SIBC TYPE I TOXIN-ANTITOXIN SYSTEM OF ESCHERICHIA COLI.” 2012. Web. 23 Feb 2020.

Vancouver:

Mok W(K. DECODING TOXICITY: CHARACTERIZATION OF THE IBSC/SIBC TYPE I TOXIN-ANTITOXIN SYSTEM OF ESCHERICHIA COLI. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12530.

Council of Science Editors:

Mok W(K. DECODING TOXICITY: CHARACTERIZATION OF THE IBSC/SIBC TYPE I TOXIN-ANTITOXIN SYSTEM OF ESCHERICHIA COLI. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12530


McMaster University

29. Bysice, Andrew. Possible Intrinsic adjuvanticity of the Amb a 1 (Ambrosia artemisiifolia :Ragweed) allergen.

Degree: MSc, 2012, McMaster University

Amb a 1 is the major allergen found in ragweed. Our observations have suggested that Amb a 1 may bind lipopolysaccharide (LPS), which would… (more)

Subjects/Keywords: Allergy; Ragweed; Immunology; LPS; Immune System Diseases; Molecular Biology; Immune System Diseases

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APA (6th Edition):

Bysice, A. (2012). Possible Intrinsic adjuvanticity of the Amb a 1 (Ambrosia artemisiifolia :Ragweed) allergen. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12634

Chicago Manual of Style (16th Edition):

Bysice, Andrew. “Possible Intrinsic adjuvanticity of the Amb a 1 (Ambrosia artemisiifolia :Ragweed) allergen.” 2012. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12634.

MLA Handbook (7th Edition):

Bysice, Andrew. “Possible Intrinsic adjuvanticity of the Amb a 1 (Ambrosia artemisiifolia :Ragweed) allergen.” 2012. Web. 23 Feb 2020.

Vancouver:

Bysice A. Possible Intrinsic adjuvanticity of the Amb a 1 (Ambrosia artemisiifolia :Ragweed) allergen. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12634.

Council of Science Editors:

Bysice A. Possible Intrinsic adjuvanticity of the Amb a 1 (Ambrosia artemisiifolia :Ragweed) allergen. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12634


McMaster University

30. Pengelly, Kate L. Characterization of Erythromycin Esterases: A Genomic Enzymology Approach to Macrolide Resistance.

Degree: MSc, 2010, McMaster University

Enzymatic inactivation of antibiotics is a successful strategy employed by antibiotic resistant clinical pathogens. Genes coding for the antibiotic inactivating enzyme erythromycin esterase, or… (more)

Subjects/Keywords: Biochemistry; Biochemistry

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APA (6th Edition):

Pengelly, K. L. (2010). Characterization of Erythromycin Esterases: A Genomic Enzymology Approach to Macrolide Resistance. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12688

Chicago Manual of Style (16th Edition):

Pengelly, Kate L. “Characterization of Erythromycin Esterases: A Genomic Enzymology Approach to Macrolide Resistance.” 2010. Masters Thesis, McMaster University. Accessed February 23, 2020. http://hdl.handle.net/11375/12688.

MLA Handbook (7th Edition):

Pengelly, Kate L. “Characterization of Erythromycin Esterases: A Genomic Enzymology Approach to Macrolide Resistance.” 2010. Web. 23 Feb 2020.

Vancouver:

Pengelly KL. Characterization of Erythromycin Esterases: A Genomic Enzymology Approach to Macrolide Resistance. [Internet] [Masters thesis]. McMaster University; 2010. [cited 2020 Feb 23]. Available from: http://hdl.handle.net/11375/12688.

Council of Science Editors:

Pengelly KL. Characterization of Erythromycin Esterases: A Genomic Enzymology Approach to Macrolide Resistance. [Masters Thesis]. McMaster University; 2010. Available from: http://hdl.handle.net/11375/12688

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