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You searched for subject:(Microbiology AND Immunology). Showing records 1 – 30 of 1454 total matches.

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Wright State University

1. Alshehri, Ali Awadh. Cell Viability, Cytoskeleton Organization and Cytokines Secretion of RAW 264.7 Macrophages Exposed to Gram-Negative Bacterial Components.

Degree: MS, Microbiology and Immunology, 2016, Wright State University

 Macrophages play an important role in innate immunity by controlling cellular responses. In this study, the effects of gram-negative bacterial components (Flagellin, lipoprotein, lipopolysaccharides (LPS),… (more)

Subjects/Keywords: Immunology; Microbiology; immunology; microbiology

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APA (6th Edition):

Alshehri, A. A. (2016). Cell Viability, Cytoskeleton Organization and Cytokines Secretion of RAW 264.7 Macrophages Exposed to Gram-Negative Bacterial Components. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1481857962791924

Chicago Manual of Style (16th Edition):

Alshehri, Ali Awadh. “Cell Viability, Cytoskeleton Organization and Cytokines Secretion of RAW 264.7 Macrophages Exposed to Gram-Negative Bacterial Components.” 2016. Masters Thesis, Wright State University. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1481857962791924.

MLA Handbook (7th Edition):

Alshehri, Ali Awadh. “Cell Viability, Cytoskeleton Organization and Cytokines Secretion of RAW 264.7 Macrophages Exposed to Gram-Negative Bacterial Components.” 2016. Web. 31 Oct 2020.

Vancouver:

Alshehri AA. Cell Viability, Cytoskeleton Organization and Cytokines Secretion of RAW 264.7 Macrophages Exposed to Gram-Negative Bacterial Components. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1481857962791924.

Council of Science Editors:

Alshehri AA. Cell Viability, Cytoskeleton Organization and Cytokines Secretion of RAW 264.7 Macrophages Exposed to Gram-Negative Bacterial Components. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1481857962791924


Wright State University

2. Alwethaynani, Maher Salem. The Expression of Aryl Hydrocarbon Receptor in RAW 264.7 Macrophages in the Presence of SOCS1 Peptide and SOCS3 Peptide Mimetic and Cells Infected with HSV-1.

Degree: MS, Microbiology and Immunology, 2016, Wright State University

 Macrophages play a crucial role for our immune system and protect our body from infection. Suppressor of cytokine signaling (SOCS) proteins negatively regulate cytokine receptor… (more)

Subjects/Keywords: Immunology; Microbiology; Immunology; Microbiology

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APA (6th Edition):

Alwethaynani, M. S. (2016). The Expression of Aryl Hydrocarbon Receptor in RAW 264.7 Macrophages in the Presence of SOCS1 Peptide and SOCS3 Peptide Mimetic and Cells Infected with HSV-1. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1484183267272414

Chicago Manual of Style (16th Edition):

Alwethaynani, Maher Salem. “The Expression of Aryl Hydrocarbon Receptor in RAW 264.7 Macrophages in the Presence of SOCS1 Peptide and SOCS3 Peptide Mimetic and Cells Infected with HSV-1.” 2016. Masters Thesis, Wright State University. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1484183267272414.

MLA Handbook (7th Edition):

Alwethaynani, Maher Salem. “The Expression of Aryl Hydrocarbon Receptor in RAW 264.7 Macrophages in the Presence of SOCS1 Peptide and SOCS3 Peptide Mimetic and Cells Infected with HSV-1.” 2016. Web. 31 Oct 2020.

Vancouver:

Alwethaynani MS. The Expression of Aryl Hydrocarbon Receptor in RAW 264.7 Macrophages in the Presence of SOCS1 Peptide and SOCS3 Peptide Mimetic and Cells Infected with HSV-1. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1484183267272414.

Council of Science Editors:

Alwethaynani MS. The Expression of Aryl Hydrocarbon Receptor in RAW 264.7 Macrophages in the Presence of SOCS1 Peptide and SOCS3 Peptide Mimetic and Cells Infected with HSV-1. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1484183267272414


Wright State University

3. Alyahya, Khalid Abdullah. Effect of Exposure of Raw264.7 Macrophages to Salmonella typhimuriumComponents on Cell Viability, Cytoskeleton Re-arrangement and Cytokine Secretion.

Degree: MS, Microbiology and Immunology, 2017, Wright State University

 Innate immune system plays an important role in individual’s protection against pathogens and in activation of adaptive immune system. Utilizing RAW 264.7 murine macrophages as… (more)

Subjects/Keywords: Microbiology; Immunology; microbiology; immunology

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APA (6th Edition):

Alyahya, K. A. (2017). Effect of Exposure of Raw264.7 Macrophages to Salmonella typhimuriumComponents on Cell Viability, Cytoskeleton Re-arrangement and Cytokine Secretion. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1513349387756891

Chicago Manual of Style (16th Edition):

Alyahya, Khalid Abdullah. “Effect of Exposure of Raw264.7 Macrophages to Salmonella typhimuriumComponents on Cell Viability, Cytoskeleton Re-arrangement and Cytokine Secretion.” 2017. Masters Thesis, Wright State University. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1513349387756891.

MLA Handbook (7th Edition):

Alyahya, Khalid Abdullah. “Effect of Exposure of Raw264.7 Macrophages to Salmonella typhimuriumComponents on Cell Viability, Cytoskeleton Re-arrangement and Cytokine Secretion.” 2017. Web. 31 Oct 2020.

Vancouver:

Alyahya KA. Effect of Exposure of Raw264.7 Macrophages to Salmonella typhimuriumComponents on Cell Viability, Cytoskeleton Re-arrangement and Cytokine Secretion. [Internet] [Masters thesis]. Wright State University; 2017. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1513349387756891.

Council of Science Editors:

Alyahya KA. Effect of Exposure of Raw264.7 Macrophages to Salmonella typhimuriumComponents on Cell Viability, Cytoskeleton Re-arrangement and Cytokine Secretion. [Masters Thesis]. Wright State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1513349387756891


Wright State University

4. Alajman, Amal Fahad. Comparing Antibody-Coated Immune Beads With Flow Cytometry to Measure ß-2-Microglubulin+ Murine Spleen Cells.

Degree: MS, Microbiology and Immunology, 2016, Wright State University

 In diseases like AIDS, Multiple Myeloma, Multiple Sclerosis (MS), Type 1 Diabetes, and Systemic Lupus Erythromatosus the detection of major histocompatibility complex type 1 molecules… (more)

Subjects/Keywords: Microbiology; Immunology; microbiology; immunology

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APA (6th Edition):

Alajman, A. F. (2016). Comparing Antibody-Coated Immune Beads With Flow Cytometry to Measure ß-2-Microglubulin+ Murine Spleen Cells. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1464188382

Chicago Manual of Style (16th Edition):

Alajman, Amal Fahad. “Comparing Antibody-Coated Immune Beads With Flow Cytometry to Measure ß-2-Microglubulin+ Murine Spleen Cells.” 2016. Masters Thesis, Wright State University. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1464188382.

MLA Handbook (7th Edition):

Alajman, Amal Fahad. “Comparing Antibody-Coated Immune Beads With Flow Cytometry to Measure ß-2-Microglubulin+ Murine Spleen Cells.” 2016. Web. 31 Oct 2020.

Vancouver:

Alajman AF. Comparing Antibody-Coated Immune Beads With Flow Cytometry to Measure ß-2-Microglubulin+ Murine Spleen Cells. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464188382.

Council of Science Editors:

Alajman AF. Comparing Antibody-Coated Immune Beads With Flow Cytometry to Measure ß-2-Microglubulin+ Murine Spleen Cells. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464188382


Wright State University

5. Almutairi, Mubarak. The Impact of HSV-1 Infection, SOCS1 peptide, and SOCS3 peptide mimetic on CellViability, Morphology, and Cytoskeleton Proteins of Unpolarized and Cytokine-PolarizedM1 RAW 264.7 Murine Macrophages.

Degree: MS, Microbiology and Immunology, 2016, Wright State University

 Mubarak Huraysan Almutairi. M.S. Department of Microbiology and Immunology, Wright StateUniversity, 2016. The Impact of HSV-1 Infection, SOCS1 peptide, and SOCS3 peptide mimeticon Cell Viability,… (more)

Subjects/Keywords: Microbiology; Immunology; microbiology; immunology

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APA (6th Edition):

Almutairi, M. (2016). The Impact of HSV-1 Infection, SOCS1 peptide, and SOCS3 peptide mimetic on CellViability, Morphology, and Cytoskeleton Proteins of Unpolarized and Cytokine-PolarizedM1 RAW 264.7 Murine Macrophages. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1464308879

Chicago Manual of Style (16th Edition):

Almutairi, Mubarak. “The Impact of HSV-1 Infection, SOCS1 peptide, and SOCS3 peptide mimetic on CellViability, Morphology, and Cytoskeleton Proteins of Unpolarized and Cytokine-PolarizedM1 RAW 264.7 Murine Macrophages.” 2016. Masters Thesis, Wright State University. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1464308879.

MLA Handbook (7th Edition):

Almutairi, Mubarak. “The Impact of HSV-1 Infection, SOCS1 peptide, and SOCS3 peptide mimetic on CellViability, Morphology, and Cytoskeleton Proteins of Unpolarized and Cytokine-PolarizedM1 RAW 264.7 Murine Macrophages.” 2016. Web. 31 Oct 2020.

Vancouver:

Almutairi M. The Impact of HSV-1 Infection, SOCS1 peptide, and SOCS3 peptide mimetic on CellViability, Morphology, and Cytoskeleton Proteins of Unpolarized and Cytokine-PolarizedM1 RAW 264.7 Murine Macrophages. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464308879.

Council of Science Editors:

Almutairi M. The Impact of HSV-1 Infection, SOCS1 peptide, and SOCS3 peptide mimetic on CellViability, Morphology, and Cytoskeleton Proteins of Unpolarized and Cytokine-PolarizedM1 RAW 264.7 Murine Macrophages. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464308879


Wright State University

6. Sharma, Hanoor. Identification of Protein-Protein Interactions of Amyotrophic Lateral Sclerosis Associated Protein TDP-43.

Degree: MS, Microbiology and Immunology, 2016, Wright State University

 Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease caused by progressive degeneration of upper and lower motor neurons in the brain and spinal cord. Multiple… (more)

Subjects/Keywords: Microbiology; Immunology; microbiology; immunology

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APA (6th Edition):

Sharma, H. (2016). Identification of Protein-Protein Interactions of Amyotrophic Lateral Sclerosis Associated Protein TDP-43. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1464713500

Chicago Manual of Style (16th Edition):

Sharma, Hanoor. “Identification of Protein-Protein Interactions of Amyotrophic Lateral Sclerosis Associated Protein TDP-43.” 2016. Masters Thesis, Wright State University. Accessed October 31, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1464713500.

MLA Handbook (7th Edition):

Sharma, Hanoor. “Identification of Protein-Protein Interactions of Amyotrophic Lateral Sclerosis Associated Protein TDP-43.” 2016. Web. 31 Oct 2020.

Vancouver:

Sharma H. Identification of Protein-Protein Interactions of Amyotrophic Lateral Sclerosis Associated Protein TDP-43. [Internet] [Masters thesis]. Wright State University; 2016. [cited 2020 Oct 31]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464713500.

Council of Science Editors:

Sharma H. Identification of Protein-Protein Interactions of Amyotrophic Lateral Sclerosis Associated Protein TDP-43. [Masters Thesis]. Wright State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1464713500


University of California – Berkeley

7. Monroe, Kathryn McGee. Type I Interferon is Not Just for Viruses: Cytosolic Sensing of Bacterial Nucleic Acids.

Degree: Molecular & Cell Biology, 2011, University of California – Berkeley

 Initial detection of invading microorganisms is one of the primary tasks of the innate immune system. However, the molecular mechanisms by which pathogens are recognized… (more)

Subjects/Keywords: Immunology; Microbiology

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APA (6th Edition):

Monroe, K. M. (2011). Type I Interferon is Not Just for Viruses: Cytosolic Sensing of Bacterial Nucleic Acids. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/8d17k8vv

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):

Monroe, Kathryn McGee. “Type I Interferon is Not Just for Viruses: Cytosolic Sensing of Bacterial Nucleic Acids.” 2011. Thesis, University of California – Berkeley. Accessed October 31, 2020. http://www.escholarship.org/uc/item/8d17k8vv.

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

MLA Handbook (7th Edition):

Monroe, Kathryn McGee. “Type I Interferon is Not Just for Viruses: Cytosolic Sensing of Bacterial Nucleic Acids.” 2011. Web. 31 Oct 2020.

Vancouver:

Monroe KM. Type I Interferon is Not Just for Viruses: Cytosolic Sensing of Bacterial Nucleic Acids. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/8d17k8vv.

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

Council of Science Editors:

Monroe KM. Type I Interferon is Not Just for Viruses: Cytosolic Sensing of Bacterial Nucleic Acids. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/8d17k8vv

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


UCLA

8. Keegan, Caroline. Mycobacterium tuberculosis tRNA triggers TLR8 to induce a pathway for Th1 cell instruction.

Degree: Microbiology, Immunology, & Molecular Genetics, 2016, UCLA

 Mycobacterium tuberculosis, the etiologic agent of tuberculosis, has infected one third of the world’s population and is one of the leading global infectious disease threats.… (more)

Subjects/Keywords: Immunology; Microbiology

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APA (6th Edition):

Keegan, C. (2016). Mycobacterium tuberculosis tRNA triggers TLR8 to induce a pathway for Th1 cell instruction. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/5mn9477s

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):

Keegan, Caroline. “Mycobacterium tuberculosis tRNA triggers TLR8 to induce a pathway for Th1 cell instruction.” 2016. Thesis, UCLA. Accessed October 31, 2020. http://www.escholarship.org/uc/item/5mn9477s.

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

MLA Handbook (7th Edition):

Keegan, Caroline. “Mycobacterium tuberculosis tRNA triggers TLR8 to induce a pathway for Th1 cell instruction.” 2016. Web. 31 Oct 2020.

Vancouver:

Keegan C. Mycobacterium tuberculosis tRNA triggers TLR8 to induce a pathway for Th1 cell instruction. [Internet] [Thesis]. UCLA; 2016. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/5mn9477s.

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

Council of Science Editors:

Keegan C. Mycobacterium tuberculosis tRNA triggers TLR8 to induce a pathway for Th1 cell instruction. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/5mn9477s

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


University of California – San Diego

9. Escajadillo, Tamara. Targeting Bacterial Pore Forming Toxins: Implications for Virulence Based Adjunctive Therapy for Invasive Bacterial Infections.

Degree: Biomedical Sciences, 2018, University of California – San Diego

 While there is pressing concern over the development of antibiotic resistance, many non-resistant pathogens are capable of causing diseases of such severity that antibiotic treatment… (more)

Subjects/Keywords: Microbiology; Immunology

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APA (6th Edition):

Escajadillo, T. (2018). Targeting Bacterial Pore Forming Toxins: Implications for Virulence Based Adjunctive Therapy for Invasive Bacterial Infections. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/4rn2t2t5

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):

Escajadillo, Tamara. “Targeting Bacterial Pore Forming Toxins: Implications for Virulence Based Adjunctive Therapy for Invasive Bacterial Infections.” 2018. Thesis, University of California – San Diego. Accessed October 31, 2020. http://www.escholarship.org/uc/item/4rn2t2t5.

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

MLA Handbook (7th Edition):

Escajadillo, Tamara. “Targeting Bacterial Pore Forming Toxins: Implications for Virulence Based Adjunctive Therapy for Invasive Bacterial Infections.” 2018. Web. 31 Oct 2020.

Vancouver:

Escajadillo T. Targeting Bacterial Pore Forming Toxins: Implications for Virulence Based Adjunctive Therapy for Invasive Bacterial Infections. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/4rn2t2t5.

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

Council of Science Editors:

Escajadillo T. Targeting Bacterial Pore Forming Toxins: Implications for Virulence Based Adjunctive Therapy for Invasive Bacterial Infections. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/4rn2t2t5

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


Vanderbilt University

10. Lewis, Nuruddeen. Arginase, Nitric Oxide, and the Defective Immune Response to Helicobacter pylori.

Degree: PhD, Cancer Biology, 2011, Vanderbilt University

 Helicobacter pylori infection persists for the life of the host due to the failure of the immune response to eradicate the bacterium. Determining the mechanisms… (more)

Subjects/Keywords: Immunology; Microbiology

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APA (6th Edition):

Lewis, N. (2011). Arginase, Nitric Oxide, and the Defective Immune Response to Helicobacter pylori. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10518

Chicago Manual of Style (16th Edition):

Lewis, Nuruddeen. “Arginase, Nitric Oxide, and the Defective Immune Response to Helicobacter pylori.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed October 31, 2020. http://hdl.handle.net/1803/10518.

MLA Handbook (7th Edition):

Lewis, Nuruddeen. “Arginase, Nitric Oxide, and the Defective Immune Response to Helicobacter pylori.” 2011. Web. 31 Oct 2020.

Vancouver:

Lewis N. Arginase, Nitric Oxide, and the Defective Immune Response to Helicobacter pylori. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1803/10518.

Council of Science Editors:

Lewis N. Arginase, Nitric Oxide, and the Defective Immune Response to Helicobacter pylori. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/10518


West Virginia University

11. Buskirk, Amanda Dawn. Characterization of Immune Responses to Repeated Aspergillus fumigatus Exposures.

Degree: PhD, Microbiology, Immunology, and Cell Biology, 2013, West Virginia University

 Personal exposures to A. fumigatus are associated with a variety of adverse health outcomes, including invasive aspergillosis, allergic sensitization, and asthma. Due to the high… (more)

Subjects/Keywords: Immunology; Microbiology

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APA (6th Edition):

Buskirk, A. D. (2013). Characterization of Immune Responses to Repeated Aspergillus fumigatus Exposures. (Doctoral Dissertation). West Virginia University. Retrieved from https://doi.org/10.33915/etd.4954 ; https://researchrepository.wvu.edu/etd/4954

Chicago Manual of Style (16th Edition):

Buskirk, Amanda Dawn. “Characterization of Immune Responses to Repeated Aspergillus fumigatus Exposures.” 2013. Doctoral Dissertation, West Virginia University. Accessed October 31, 2020. https://doi.org/10.33915/etd.4954 ; https://researchrepository.wvu.edu/etd/4954.

MLA Handbook (7th Edition):

Buskirk, Amanda Dawn. “Characterization of Immune Responses to Repeated Aspergillus fumigatus Exposures.” 2013. Web. 31 Oct 2020.

Vancouver:

Buskirk AD. Characterization of Immune Responses to Repeated Aspergillus fumigatus Exposures. [Internet] [Doctoral dissertation]. West Virginia University; 2013. [cited 2020 Oct 31]. Available from: https://doi.org/10.33915/etd.4954 ; https://researchrepository.wvu.edu/etd/4954.

Council of Science Editors:

Buskirk AD. Characterization of Immune Responses to Repeated Aspergillus fumigatus Exposures. [Doctoral Dissertation]. West Virginia University; 2013. Available from: https://doi.org/10.33915/etd.4954 ; https://researchrepository.wvu.edu/etd/4954


University of California – San Francisco

12. Price, April. Investigations into the Cellular Sources of Type 2 Cytokines and Interleukin-17A using Cytokine Reporter Mice.

Degree: Biomedical Sciences, 2012, University of California – San Francisco

 Cytokines play a pivotal role in the maintenance of homeostasis and in the coordination of immune responses. Our lab has designed a variety of cytokine… (more)

Subjects/Keywords: Immunology; Microbiology

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APA (6th Edition):

Price, A. (2012). Investigations into the Cellular Sources of Type 2 Cytokines and Interleukin-17A using Cytokine Reporter Mice. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2hz5b6j7

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):

Price, April. “Investigations into the Cellular Sources of Type 2 Cytokines and Interleukin-17A using Cytokine Reporter Mice.” 2012. Thesis, University of California – San Francisco. Accessed October 31, 2020. http://www.escholarship.org/uc/item/2hz5b6j7.

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

MLA Handbook (7th Edition):

Price, April. “Investigations into the Cellular Sources of Type 2 Cytokines and Interleukin-17A using Cytokine Reporter Mice.” 2012. Web. 31 Oct 2020.

Vancouver:

Price A. Investigations into the Cellular Sources of Type 2 Cytokines and Interleukin-17A using Cytokine Reporter Mice. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/2hz5b6j7.

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

Council of Science Editors:

Price A. Investigations into the Cellular Sources of Type 2 Cytokines and Interleukin-17A using Cytokine Reporter Mice. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/2hz5b6j7

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


McGill University

13. Mitsopoulos, Panagiotis. Functional characterization of stomatin-like protein 2.

Degree: PhD, Department of Microbiology and Immunology, 2017, McGill University

 Stomatin-like protein (SLP)-2 est une protéine largement exprimée et hautement conservée qui a été identifiée lors d'une analyse protéomique des microdomaines insoluble enrichis en glycolipides… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Mitsopoulos, P. (2017). Functional characterization of stomatin-like protein 2. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/2r36v080z.pdf ; https://escholarship.mcgill.ca/concern/theses/wm117r250

Chicago Manual of Style (16th Edition):

Mitsopoulos, Panagiotis. “Functional characterization of stomatin-like protein 2.” 2017. Doctoral Dissertation, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/2r36v080z.pdf ; https://escholarship.mcgill.ca/concern/theses/wm117r250.

MLA Handbook (7th Edition):

Mitsopoulos, Panagiotis. “Functional characterization of stomatin-like protein 2.” 2017. Web. 31 Oct 2020.

Vancouver:

Mitsopoulos P. Functional characterization of stomatin-like protein 2. [Internet] [Doctoral dissertation]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/2r36v080z.pdf ; https://escholarship.mcgill.ca/concern/theses/wm117r250.

Council of Science Editors:

Mitsopoulos P. Functional characterization of stomatin-like protein 2. [Doctoral Dissertation]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/2r36v080z.pdf ; https://escholarship.mcgill.ca/concern/theses/wm117r250


McGill University

14. Peres, Adam. Regulatory role of monocytes and macrophages in infection and immunity.

Degree: PhD, Department of Microbiology and Immunology, 2018, McGill University

 Le système immunitaire possède un vaste réseau de mécanismes de défense essentiel à la survie de l'hôte, mais qui peut aussi lui être néfaste en… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Peres, A. (2018). Regulatory role of monocytes and macrophages in infection and immunity. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/707959989.pdf ; https://escholarship.mcgill.ca/concern/theses/rx913s20f

Chicago Manual of Style (16th Edition):

Peres, Adam. “Regulatory role of monocytes and macrophages in infection and immunity.” 2018. Doctoral Dissertation, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/707959989.pdf ; https://escholarship.mcgill.ca/concern/theses/rx913s20f.

MLA Handbook (7th Edition):

Peres, Adam. “Regulatory role of monocytes and macrophages in infection and immunity.” 2018. Web. 31 Oct 2020.

Vancouver:

Peres A. Regulatory role of monocytes and macrophages in infection and immunity. [Internet] [Doctoral dissertation]. McGill University; 2018. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/707959989.pdf ; https://escholarship.mcgill.ca/concern/theses/rx913s20f.

Council of Science Editors:

Peres A. Regulatory role of monocytes and macrophages in infection and immunity. [Doctoral Dissertation]. McGill University; 2018. Available from: https://escholarship.mcgill.ca/downloads/707959989.pdf ; https://escholarship.mcgill.ca/concern/theses/rx913s20f


McGill University

15. Sinha, Anshul. PmrC and CptA-mediated regulation of outer membrane vesicle production in «Citrobacter rodentium».

Degree: MS, Department of Microbiology and Immunology, 2018, McGill University

Les vésicules de membrane externe (OMV) sont des structures sphériques produites par toutes les bactéries à Gram négatif. Puisqu'elles dérivent de l'enveloppe des cellules, les… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Sinha, A. (2018). PmrC and CptA-mediated regulation of outer membrane vesicle production in «Citrobacter rodentium». (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/z890rw734.pdf ; https://escholarship.mcgill.ca/concern/theses/3j333464t

Chicago Manual of Style (16th Edition):

Sinha, Anshul. “PmrC and CptA-mediated regulation of outer membrane vesicle production in «Citrobacter rodentium».” 2018. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/z890rw734.pdf ; https://escholarship.mcgill.ca/concern/theses/3j333464t.

MLA Handbook (7th Edition):

Sinha, Anshul. “PmrC and CptA-mediated regulation of outer membrane vesicle production in «Citrobacter rodentium».” 2018. Web. 31 Oct 2020.

Vancouver:

Sinha A. PmrC and CptA-mediated regulation of outer membrane vesicle production in «Citrobacter rodentium». [Internet] [Masters thesis]. McGill University; 2018. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/z890rw734.pdf ; https://escholarship.mcgill.ca/concern/theses/3j333464t.

Council of Science Editors:

Sinha A. PmrC and CptA-mediated regulation of outer membrane vesicle production in «Citrobacter rodentium». [Masters Thesis]. McGill University; 2018. Available from: https://escholarship.mcgill.ca/downloads/z890rw734.pdf ; https://escholarship.mcgill.ca/concern/theses/3j333464t


McGill University

16. Shapiro, Janna. Case studies in vaccine evaluation.

Degree: MS, Department of Microbiology and Immunology, 2018, McGill University

On estime que les vaccins permettent d'éviter 2,5 millions de décès chaque année. Comme pour toute intervention de santé publique, les vaccins passent par de… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Shapiro, J. (2018). Case studies in vaccine evaluation. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/fb494b600.pdf ; https://escholarship.mcgill.ca/concern/theses/dz010s406

Chicago Manual of Style (16th Edition):

Shapiro, Janna. “Case studies in vaccine evaluation.” 2018. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/fb494b600.pdf ; https://escholarship.mcgill.ca/concern/theses/dz010s406.

MLA Handbook (7th Edition):

Shapiro, Janna. “Case studies in vaccine evaluation.” 2018. Web. 31 Oct 2020.

Vancouver:

Shapiro J. Case studies in vaccine evaluation. [Internet] [Masters thesis]. McGill University; 2018. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/fb494b600.pdf ; https://escholarship.mcgill.ca/concern/theses/dz010s406.

Council of Science Editors:

Shapiro J. Case studies in vaccine evaluation. [Masters Thesis]. McGill University; 2018. Available from: https://escholarship.mcgill.ca/downloads/fb494b600.pdf ; https://escholarship.mcgill.ca/concern/theses/dz010s406


McGill University

17. Smith, Logan. IL-10 reduces CD8 T cell antigen sensitivity during the establishment of chronic viral infection by modifying N-glycan branching.

Degree: MS, Department of Microbiology and Immunology, 2017, McGill University

Chronic viral infections remain a global health concern. The early events that facilitate viral persistence have been linked to the activity of the immunoregulatory cytokine… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Smith, L. (2017). IL-10 reduces CD8 T cell antigen sensitivity during the establishment of chronic viral infection by modifying N-glycan branching. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/2n49t437n.pdf ; https://escholarship.mcgill.ca/concern/theses/th83m182w

Chicago Manual of Style (16th Edition):

Smith, Logan. “IL-10 reduces CD8 T cell antigen sensitivity during the establishment of chronic viral infection by modifying N-glycan branching.” 2017. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/2n49t437n.pdf ; https://escholarship.mcgill.ca/concern/theses/th83m182w.

MLA Handbook (7th Edition):

Smith, Logan. “IL-10 reduces CD8 T cell antigen sensitivity during the establishment of chronic viral infection by modifying N-glycan branching.” 2017. Web. 31 Oct 2020.

Vancouver:

Smith L. IL-10 reduces CD8 T cell antigen sensitivity during the establishment of chronic viral infection by modifying N-glycan branching. [Internet] [Masters thesis]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/2n49t437n.pdf ; https://escholarship.mcgill.ca/concern/theses/th83m182w.

Council of Science Editors:

Smith L. IL-10 reduces CD8 T cell antigen sensitivity during the establishment of chronic viral infection by modifying N-glycan branching. [Masters Thesis]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/2n49t437n.pdf ; https://escholarship.mcgill.ca/concern/theses/th83m182w


McGill University

18. Bagherzadeh Yazdchi, Sahar. The role of mammalian sterile 20-like kinase 1 in humoral immunity.

Degree: PhD, Department of Microbiology and Immunology, 2018, McGill University

 La protéine Sérine/Thréonine kinase 1 mammalienne (Mst1) est l'une des protéines clés de la voie métabolique Hippo qui régule de multiples fonctions biologiques telles que… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Bagherzadeh Yazdchi, S. (2018). The role of mammalian sterile 20-like kinase 1 in humoral immunity. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/c534fr17j.pdf ; https://escholarship.mcgill.ca/concern/theses/h415pc85m

Chicago Manual of Style (16th Edition):

Bagherzadeh Yazdchi, Sahar. “The role of mammalian sterile 20-like kinase 1 in humoral immunity.” 2018. Doctoral Dissertation, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/c534fr17j.pdf ; https://escholarship.mcgill.ca/concern/theses/h415pc85m.

MLA Handbook (7th Edition):

Bagherzadeh Yazdchi, Sahar. “The role of mammalian sterile 20-like kinase 1 in humoral immunity.” 2018. Web. 31 Oct 2020.

Vancouver:

Bagherzadeh Yazdchi S. The role of mammalian sterile 20-like kinase 1 in humoral immunity. [Internet] [Doctoral dissertation]. McGill University; 2018. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/c534fr17j.pdf ; https://escholarship.mcgill.ca/concern/theses/h415pc85m.

Council of Science Editors:

Bagherzadeh Yazdchi S. The role of mammalian sterile 20-like kinase 1 in humoral immunity. [Doctoral Dissertation]. McGill University; 2018. Available from: https://escholarship.mcgill.ca/downloads/c534fr17j.pdf ; https://escholarship.mcgill.ca/concern/theses/h415pc85m


McGill University

19. Carnevale, Giustino. The regulation of skin immunity by CD109 with relevance to psoriatic-like inflammation.

Degree: MS, Department of Microbiology and Immunology, 2016, McGill University

Mammalian skin contains a complex network of immune and stromal cell types that serve an indispensable role in host defense against environmental insults and invasion… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Carnevale, G. (2016). The regulation of skin immunity by CD109 with relevance to psoriatic-like inflammation. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/d217qs417.pdf ; https://escholarship.mcgill.ca/concern/theses/jm214r93c

Chicago Manual of Style (16th Edition):

Carnevale, Giustino. “The regulation of skin immunity by CD109 with relevance to psoriatic-like inflammation.” 2016. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/d217qs417.pdf ; https://escholarship.mcgill.ca/concern/theses/jm214r93c.

MLA Handbook (7th Edition):

Carnevale, Giustino. “The regulation of skin immunity by CD109 with relevance to psoriatic-like inflammation.” 2016. Web. 31 Oct 2020.

Vancouver:

Carnevale G. The regulation of skin immunity by CD109 with relevance to psoriatic-like inflammation. [Internet] [Masters thesis]. McGill University; 2016. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/d217qs417.pdf ; https://escholarship.mcgill.ca/concern/theses/jm214r93c.

Council of Science Editors:

Carnevale G. The regulation of skin immunity by CD109 with relevance to psoriatic-like inflammation. [Masters Thesis]. McGill University; 2016. Available from: https://escholarship.mcgill.ca/downloads/d217qs417.pdf ; https://escholarship.mcgill.ca/concern/theses/jm214r93c


McGill University

20. Ghanem, Marwan. Using «Mycobacterium kansasii» as a proxy to study the pathoevolution of «M. tuberculosis».

Degree: MS, Department of Microbiology and Immunology, 2018, McGill University

On a yearly basis, 1.8 million people lose their lives due to tuberculosis, making it the single deadliest infectious disease in the world. M. tuberculosis… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Ghanem, M. (2018). Using «Mycobacterium kansasii» as a proxy to study the pathoevolution of «M. tuberculosis». (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/41687k56h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h682m

Chicago Manual of Style (16th Edition):

Ghanem, Marwan. “Using «Mycobacterium kansasii» as a proxy to study the pathoevolution of «M. tuberculosis».” 2018. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/41687k56h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h682m.

MLA Handbook (7th Edition):

Ghanem, Marwan. “Using «Mycobacterium kansasii» as a proxy to study the pathoevolution of «M. tuberculosis».” 2018. Web. 31 Oct 2020.

Vancouver:

Ghanem M. Using «Mycobacterium kansasii» as a proxy to study the pathoevolution of «M. tuberculosis». [Internet] [Masters thesis]. McGill University; 2018. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/41687k56h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h682m.

Council of Science Editors:

Ghanem M. Using «Mycobacterium kansasii» as a proxy to study the pathoevolution of «M. tuberculosis». [Masters Thesis]. McGill University; 2018. Available from: https://escholarship.mcgill.ca/downloads/41687k56h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h682m


McGill University

21. Damian, Andreea. Role of the aryl hydrocarbon receptor in disease tolerance to «staphylococcus aureus».

Degree: MS, Department of Microbiology and Immunology, 2017, McGill University

Staphylococcus aureus (S. aureus) is a Gram-positive bacterium that commonly colonizes healthy human beings. However, S. aureus is also a frequent causative agent of serious… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Damian, A. (2017). Role of the aryl hydrocarbon receptor in disease tolerance to «staphylococcus aureus». (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/6q182n67h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h699s

Chicago Manual of Style (16th Edition):

Damian, Andreea. “Role of the aryl hydrocarbon receptor in disease tolerance to «staphylococcus aureus».” 2017. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/6q182n67h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h699s.

MLA Handbook (7th Edition):

Damian, Andreea. “Role of the aryl hydrocarbon receptor in disease tolerance to «staphylococcus aureus».” 2017. Web. 31 Oct 2020.

Vancouver:

Damian A. Role of the aryl hydrocarbon receptor in disease tolerance to «staphylococcus aureus». [Internet] [Masters thesis]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/6q182n67h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h699s.

Council of Science Editors:

Damian A. Role of the aryl hydrocarbon receptor in disease tolerance to «staphylococcus aureus». [Masters Thesis]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/6q182n67h.pdf ; https://escholarship.mcgill.ca/concern/theses/1n79h699s


McGill University

22. Van Den Ham, Kristin. Protection from experimental cerebral malaria through the attenuation of CXCR3-mediated T cell chemotaxis.

Degree: PhD, Department of Microbiology and Immunology, 2017, McGill University

 Plus de quatre-vingt-dix pays sont connus comme étant des foyers de transmission active de la malaria, ou paludisme, exposant ainsi près de la moitié de… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Van Den Ham, K. (2017). Protection from experimental cerebral malaria through the attenuation of CXCR3-mediated T cell chemotaxis. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/k35696882.pdf ; https://escholarship.mcgill.ca/concern/theses/mp48sg150

Chicago Manual of Style (16th Edition):

Van Den Ham, Kristin. “Protection from experimental cerebral malaria through the attenuation of CXCR3-mediated T cell chemotaxis.” 2017. Doctoral Dissertation, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/k35696882.pdf ; https://escholarship.mcgill.ca/concern/theses/mp48sg150.

MLA Handbook (7th Edition):

Van Den Ham, Kristin. “Protection from experimental cerebral malaria through the attenuation of CXCR3-mediated T cell chemotaxis.” 2017. Web. 31 Oct 2020.

Vancouver:

Van Den Ham K. Protection from experimental cerebral malaria through the attenuation of CXCR3-mediated T cell chemotaxis. [Internet] [Doctoral dissertation]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/k35696882.pdf ; https://escholarship.mcgill.ca/concern/theses/mp48sg150.

Council of Science Editors:

Van Den Ham K. Protection from experimental cerebral malaria through the attenuation of CXCR3-mediated T cell chemotaxis. [Doctoral Dissertation]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/k35696882.pdf ; https://escholarship.mcgill.ca/concern/theses/mp48sg150


McGill University

23. Pavey, Nils. The role of Mxi1-SR beta in the generation and homeostasis of Foxp3+ T regulatory cells.

Degree: MS, Department of Microbiology and Immunology, 2017, McGill University

Les lymphocytes T régulateurs (Treg) CD4+Foxp3+ sont des médiateurs essentiels de la tolérance au soi et du maintien de l'homéostasie. Pour cette raison, les cellules… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Pavey, N. (2017). The role of Mxi1-SR beta in the generation and homeostasis of Foxp3+ T regulatory cells. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/db78tf59f.pdf ; https://escholarship.mcgill.ca/concern/theses/7s75dg074

Chicago Manual of Style (16th Edition):

Pavey, Nils. “The role of Mxi1-SR beta in the generation and homeostasis of Foxp3+ T regulatory cells.” 2017. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/db78tf59f.pdf ; https://escholarship.mcgill.ca/concern/theses/7s75dg074.

MLA Handbook (7th Edition):

Pavey, Nils. “The role of Mxi1-SR beta in the generation and homeostasis of Foxp3+ T regulatory cells.” 2017. Web. 31 Oct 2020.

Vancouver:

Pavey N. The role of Mxi1-SR beta in the generation and homeostasis of Foxp3+ T regulatory cells. [Internet] [Masters thesis]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/db78tf59f.pdf ; https://escholarship.mcgill.ca/concern/theses/7s75dg074.

Council of Science Editors:

Pavey N. The role of Mxi1-SR beta in the generation and homeostasis of Foxp3+ T regulatory cells. [Masters Thesis]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/db78tf59f.pdf ; https://escholarship.mcgill.ca/concern/theses/7s75dg074


McGill University

24. Ngure, Marianne. Protein-protein interactions of the unstructured domain II of hepatitis C virus NS5A.

Degree: PhD, Department of Microbiology and Immunology, 2017, McGill University

The hepatitis C virus (HCV) non-structural 5A (NS5A) protein is a multi-functional, RNA binding protein and an essential component of the HCV replication complex. It… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Ngure, M. (2017). Protein-protein interactions of the unstructured domain II of hepatitis C virus NS5A. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/1g05ff39t.pdf ; https://escholarship.mcgill.ca/concern/theses/3197xp22w

Chicago Manual of Style (16th Edition):

Ngure, Marianne. “Protein-protein interactions of the unstructured domain II of hepatitis C virus NS5A.” 2017. Doctoral Dissertation, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/1g05ff39t.pdf ; https://escholarship.mcgill.ca/concern/theses/3197xp22w.

MLA Handbook (7th Edition):

Ngure, Marianne. “Protein-protein interactions of the unstructured domain II of hepatitis C virus NS5A.” 2017. Web. 31 Oct 2020.

Vancouver:

Ngure M. Protein-protein interactions of the unstructured domain II of hepatitis C virus NS5A. [Internet] [Doctoral dissertation]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/1g05ff39t.pdf ; https://escholarship.mcgill.ca/concern/theses/3197xp22w.

Council of Science Editors:

Ngure M. Protein-protein interactions of the unstructured domain II of hepatitis C virus NS5A. [Doctoral Dissertation]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/1g05ff39t.pdf ; https://escholarship.mcgill.ca/concern/theses/3197xp22w


McGill University

25. Ackroyd, Travis. The role of the cystic fibrosis transmembrane conductance regulator in host protection against «Citrobacter rodentium» intestinal infection.

Degree: MS, Department of Microbiology and Immunology, 2016, McGill University

La fibrose kystique (FK) est une maladie mortelle causée par des mutations dans le gène cystic fibrosis transmembrane conductance regulator (CFTR). La protéine CFTR, exprimée… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Ackroyd, T. (2016). The role of the cystic fibrosis transmembrane conductance regulator in host protection against «Citrobacter rodentium» intestinal infection. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/vm40xv36q.pdf ; https://escholarship.mcgill.ca/concern/theses/0r967626v

Chicago Manual of Style (16th Edition):

Ackroyd, Travis. “The role of the cystic fibrosis transmembrane conductance regulator in host protection against «Citrobacter rodentium» intestinal infection.” 2016. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/vm40xv36q.pdf ; https://escholarship.mcgill.ca/concern/theses/0r967626v.

MLA Handbook (7th Edition):

Ackroyd, Travis. “The role of the cystic fibrosis transmembrane conductance regulator in host protection against «Citrobacter rodentium» intestinal infection.” 2016. Web. 31 Oct 2020.

Vancouver:

Ackroyd T. The role of the cystic fibrosis transmembrane conductance regulator in host protection against «Citrobacter rodentium» intestinal infection. [Internet] [Masters thesis]. McGill University; 2016. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/vm40xv36q.pdf ; https://escholarship.mcgill.ca/concern/theses/0r967626v.

Council of Science Editors:

Ackroyd T. The role of the cystic fibrosis transmembrane conductance regulator in host protection against «Citrobacter rodentium» intestinal infection. [Masters Thesis]. McGill University; 2016. Available from: https://escholarship.mcgill.ca/downloads/vm40xv36q.pdf ; https://escholarship.mcgill.ca/concern/theses/0r967626v


McGill University

26. Ricciardi, Alessandra. Preclinical characterization of the protection and immune response elicited by immunizations with Schistosoma mansoni cathepsin B.

Degree: PhD, Department of Microbiology and Immunology, 2017, McGill University

 La schistosomiase est une maladie tropicale négligeé causée par des vers plats d'eau douce. La schistosomiase est une maladie chronique qui représente une préoccupation majeure… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Ricciardi, A. (2017). Preclinical characterization of the protection and immune response elicited by immunizations with Schistosoma mansoni cathepsin B. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/rr172071n.pdf ; https://escholarship.mcgill.ca/concern/theses/r781wj58d

Chicago Manual of Style (16th Edition):

Ricciardi, Alessandra. “Preclinical characterization of the protection and immune response elicited by immunizations with Schistosoma mansoni cathepsin B.” 2017. Doctoral Dissertation, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/rr172071n.pdf ; https://escholarship.mcgill.ca/concern/theses/r781wj58d.

MLA Handbook (7th Edition):

Ricciardi, Alessandra. “Preclinical characterization of the protection and immune response elicited by immunizations with Schistosoma mansoni cathepsin B.” 2017. Web. 31 Oct 2020.

Vancouver:

Ricciardi A. Preclinical characterization of the protection and immune response elicited by immunizations with Schistosoma mansoni cathepsin B. [Internet] [Doctoral dissertation]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/rr172071n.pdf ; https://escholarship.mcgill.ca/concern/theses/r781wj58d.

Council of Science Editors:

Ricciardi A. Preclinical characterization of the protection and immune response elicited by immunizations with Schistosoma mansoni cathepsin B. [Doctoral Dissertation]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/rr172071n.pdf ; https://escholarship.mcgill.ca/concern/theses/r781wj58d


McGill University

27. Huang, Fan. The anti-HIV-1 host protein MxB promotes cell apoptosis.

Degree: MS, Department of Microbiology and Immunology, 2017, McGill University

Il a récemment été démontré que la protéine de résistance aux Mixovirus (Mx) inductible par interferon MxB restreint l'infection au VIH-1. Avant la découverte de… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Huang, F. (2017). The anti-HIV-1 host protein MxB promotes cell apoptosis. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/wp988n61b.pdf ; https://escholarship.mcgill.ca/concern/theses/cz30pw32q

Chicago Manual of Style (16th Edition):

Huang, Fan. “The anti-HIV-1 host protein MxB promotes cell apoptosis.” 2017. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/wp988n61b.pdf ; https://escholarship.mcgill.ca/concern/theses/cz30pw32q.

MLA Handbook (7th Edition):

Huang, Fan. “The anti-HIV-1 host protein MxB promotes cell apoptosis.” 2017. Web. 31 Oct 2020.

Vancouver:

Huang F. The anti-HIV-1 host protein MxB promotes cell apoptosis. [Internet] [Masters thesis]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/wp988n61b.pdf ; https://escholarship.mcgill.ca/concern/theses/cz30pw32q.

Council of Science Editors:

Huang F. The anti-HIV-1 host protein MxB promotes cell apoptosis. [Masters Thesis]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/wp988n61b.pdf ; https://escholarship.mcgill.ca/concern/theses/cz30pw32q


McGill University

28. Bin Dhuban, Khalid. Functional characterization and biomarker discovery of FOXP3+ regulatory T cells in human health and disease.

Degree: PhD, Department of Microbiology and Immunology, 2017, McGill University

 Les lymphocytes T régulateurs (Treg), CD4+Foxp3+, sont des médiateurs fondamentaux de la tolérance périphérique face aux antigènes du soi et de l'environnement. Chez les humains,… (more)

Subjects/Keywords: Microbiology & Immunology

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APA (6th Edition):

Bin Dhuban, K. (2017). Functional characterization and biomarker discovery of FOXP3+ regulatory T cells in human health and disease. (Doctoral Dissertation). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/vt150m67d.pdf ; https://escholarship.mcgill.ca/concern/theses/w3763956w

Chicago Manual of Style (16th Edition):

Bin Dhuban, Khalid. “Functional characterization and biomarker discovery of FOXP3+ regulatory T cells in human health and disease.” 2017. Doctoral Dissertation, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/vt150m67d.pdf ; https://escholarship.mcgill.ca/concern/theses/w3763956w.

MLA Handbook (7th Edition):

Bin Dhuban, Khalid. “Functional characterization and biomarker discovery of FOXP3+ regulatory T cells in human health and disease.” 2017. Web. 31 Oct 2020.

Vancouver:

Bin Dhuban K. Functional characterization and biomarker discovery of FOXP3+ regulatory T cells in human health and disease. [Internet] [Doctoral dissertation]. McGill University; 2017. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/vt150m67d.pdf ; https://escholarship.mcgill.ca/concern/theses/w3763956w.

Council of Science Editors:

Bin Dhuban K. Functional characterization and biomarker discovery of FOXP3+ regulatory T cells in human health and disease. [Doctoral Dissertation]. McGill University; 2017. Available from: https://escholarship.mcgill.ca/downloads/vt150m67d.pdf ; https://escholarship.mcgill.ca/concern/theses/w3763956w


McGill University

29. Domi, Anisa. Identifying mechanisms responsible for regulating expression of PCGF6, a repressor of DC activation.

Degree: MS, Department of Microbiology and Immunology, 2016, McGill University

The immune system is capable of providing an intricate and well-orchestrated defense program against a variety of different threats including microbes, parasites and cancer. Dendritic… (more)

Subjects/Keywords: Microbiology & Immunology

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

APA (6th Edition):

Domi, A. (2016). Identifying mechanisms responsible for regulating expression of PCGF6, a repressor of DC activation. (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/gh93h215g.pdf ; https://escholarship.mcgill.ca/concern/theses/q237hv261

Chicago Manual of Style (16th Edition):

Domi, Anisa. “Identifying mechanisms responsible for regulating expression of PCGF6, a repressor of DC activation.” 2016. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/gh93h215g.pdf ; https://escholarship.mcgill.ca/concern/theses/q237hv261.

MLA Handbook (7th Edition):

Domi, Anisa. “Identifying mechanisms responsible for regulating expression of PCGF6, a repressor of DC activation.” 2016. Web. 31 Oct 2020.

Vancouver:

Domi A. Identifying mechanisms responsible for regulating expression of PCGF6, a repressor of DC activation. [Internet] [Masters thesis]. McGill University; 2016. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/gh93h215g.pdf ; https://escholarship.mcgill.ca/concern/theses/q237hv261.

Council of Science Editors:

Domi A. Identifying mechanisms responsible for regulating expression of PCGF6, a repressor of DC activation. [Masters Thesis]. McGill University; 2016. Available from: https://escholarship.mcgill.ca/downloads/gh93h215g.pdf ; https://escholarship.mcgill.ca/concern/theses/q237hv261


McGill University

30. Dunn, Jonathan. Harnessing the power of stem cells in vaccine against «Mycobacterium tuberculosis».

Degree: MS, Department of Microbiology and Immunology, 2016, McGill University

Mycobacterium tuberculosis (Mtb) remains one of the most successful human pathogens. Approximately two million people die of TB annually and eight to ten million new… (more)

Subjects/Keywords: Microbiology & Immunology

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

APA (6th Edition):

Dunn, J. (2016). Harnessing the power of stem cells in vaccine against «Mycobacterium tuberculosis». (Masters Thesis). McGill University. Retrieved from https://escholarship.mcgill.ca/downloads/1c18dj23p.pdf ; https://escholarship.mcgill.ca/concern/theses/gt54kq75j

Chicago Manual of Style (16th Edition):

Dunn, Jonathan. “Harnessing the power of stem cells in vaccine against «Mycobacterium tuberculosis».” 2016. Masters Thesis, McGill University. Accessed October 31, 2020. https://escholarship.mcgill.ca/downloads/1c18dj23p.pdf ; https://escholarship.mcgill.ca/concern/theses/gt54kq75j.

MLA Handbook (7th Edition):

Dunn, Jonathan. “Harnessing the power of stem cells in vaccine against «Mycobacterium tuberculosis».” 2016. Web. 31 Oct 2020.

Vancouver:

Dunn J. Harnessing the power of stem cells in vaccine against «Mycobacterium tuberculosis». [Internet] [Masters thesis]. McGill University; 2016. [cited 2020 Oct 31]. Available from: https://escholarship.mcgill.ca/downloads/1c18dj23p.pdf ; https://escholarship.mcgill.ca/concern/theses/gt54kq75j.

Council of Science Editors:

Dunn J. Harnessing the power of stem cells in vaccine against «Mycobacterium tuberculosis». [Masters Thesis]. McGill University; 2016. Available from: https://escholarship.mcgill.ca/downloads/1c18dj23p.pdf ; https://escholarship.mcgill.ca/concern/theses/gt54kq75j

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