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You searched for subject:(Health Sciences Immunology). Showing records 1 – 30 of 1021 total matches.

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1. Bearden, Melissa K. Lymphatic pump treatment mobilizes leukocytes from the gastrointestinal associated lymphiod tissue.

Degree: 2008, University of North Texas Health Science Center at Fort Worth

  Lymphatic flow and the migration of leukocytes are important to maintaining health. One treatment used to improve lymph flow is abdominal lymphatic pump treatment… (more)

Subjects/Keywords: Health Sciences; Immunology

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

APA (6th Edition):

Bearden, M. K. (2008). Lymphatic pump treatment mobilizes leukocytes from the gastrointestinal associated lymphiod tissue. (Thesis). University of North Texas Health Science Center at Fort Worth. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1459918

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):

Bearden, Melissa K. “Lymphatic pump treatment mobilizes leukocytes from the gastrointestinal associated lymphiod tissue.” 2008. Thesis, University of North Texas Health Science Center at Fort Worth. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=1459918.

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

MLA Handbook (7th Edition):

Bearden, Melissa K. “Lymphatic pump treatment mobilizes leukocytes from the gastrointestinal associated lymphiod tissue.” 2008. Web. 02 Apr 2020.

Vancouver:

Bearden MK. Lymphatic pump treatment mobilizes leukocytes from the gastrointestinal associated lymphiod tissue. [Internet] [Thesis]. University of North Texas Health Science Center at Fort Worth; 2008. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1459918.

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

Council of Science Editors:

Bearden MK. Lymphatic pump treatment mobilizes leukocytes from the gastrointestinal associated lymphiod tissue. [Thesis]. University of North Texas Health Science Center at Fort Worth; 2008. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1459918

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


The University of North Carolina at Chapel Hill

2. Gilbert, Mileka Richelle. Dendritic cell and macrophage-mediated tolerance in lupus-prone mice.

Degree: 2007, The University of North Carolina at Chapel Hill

  During infection, immune cells respond to polyclonal activators, like bacterial and viral antigens, through innate immune responses. Therefore, mechanisms to regulate the activation of… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Gilbert, M. R. (2007). Dendritic cell and macrophage-mediated tolerance in lupus-prone mice. (Thesis). The University of North Carolina at Chapel Hill. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3272567

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):

Gilbert, Mileka Richelle. “Dendritic cell and macrophage-mediated tolerance in lupus-prone mice.” 2007. Thesis, The University of North Carolina at Chapel Hill. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3272567.

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

MLA Handbook (7th Edition):

Gilbert, Mileka Richelle. “Dendritic cell and macrophage-mediated tolerance in lupus-prone mice.” 2007. Web. 02 Apr 2020.

Vancouver:

Gilbert MR. Dendritic cell and macrophage-mediated tolerance in lupus-prone mice. [Internet] [Thesis]. The University of North Carolina at Chapel Hill; 2007. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3272567.

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

Council of Science Editors:

Gilbert MR. Dendritic cell and macrophage-mediated tolerance in lupus-prone mice. [Thesis]. The University of North Carolina at Chapel Hill; 2007. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3272567

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

3. Ambrosini, Yoko Miyamoto. Innate Immunity and the Pathogenesis of Primary Biliary Cirrhosis.

Degree: 2011, University of California, Davis

  Primary biliary cirrhosis (PBC) is a human autoimmune liver disease characterized by progressive destruction of the intrahepatic biliary epithelial cells (BECs) eventually leading to… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Ambrosini, Y. M. (2011). Innate Immunity and the Pathogenesis of Primary Biliary Cirrhosis. (Thesis). University of California, Davis. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3482096

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):

Ambrosini, Yoko Miyamoto. “Innate Immunity and the Pathogenesis of Primary Biliary Cirrhosis.” 2011. Thesis, University of California, Davis. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3482096.

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

MLA Handbook (7th Edition):

Ambrosini, Yoko Miyamoto. “Innate Immunity and the Pathogenesis of Primary Biliary Cirrhosis.” 2011. Web. 02 Apr 2020.

Vancouver:

Ambrosini YM. Innate Immunity and the Pathogenesis of Primary Biliary Cirrhosis. [Internet] [Thesis]. University of California, Davis; 2011. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3482096.

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

Council of Science Editors:

Ambrosini YM. Innate Immunity and the Pathogenesis of Primary Biliary Cirrhosis. [Thesis]. University of California, Davis; 2011. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3482096

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

4. Abe, Brian Tadayoshi. The role of NFAT1 in tumor-induced CD4+ T cell tolerance.

Degree: 2012, Yeshiva University

  Tumor recognition and elimination by the immune system is key to limiting cancer development. The T cell arm of the adaptive immune system has… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Abe, B. T. (2012). The role of NFAT1 in tumor-induced CD4+ T cell tolerance. (Thesis). Yeshiva University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3500918

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):

Abe, Brian Tadayoshi. “The role of NFAT1 in tumor-induced CD4+ T cell tolerance.” 2012. Thesis, Yeshiva University. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3500918.

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

MLA Handbook (7th Edition):

Abe, Brian Tadayoshi. “The role of NFAT1 in tumor-induced CD4+ T cell tolerance.” 2012. Web. 02 Apr 2020.

Vancouver:

Abe BT. The role of NFAT1 in tumor-induced CD4+ T cell tolerance. [Internet] [Thesis]. Yeshiva University; 2012. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3500918.

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

Council of Science Editors:

Abe BT. The role of NFAT1 in tumor-induced CD4+ T cell tolerance. [Thesis]. Yeshiva University; 2012. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3500918

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


University of Cincinnati

5. Lin, Adora A. The CD4+ T cell response to CNS viral infection.

Degree: 2009, University of Cincinnati

  T cell-mediated pathology is a major cause of disease in both infection and autoimmunity. While T cell responses provide protection from pathogens, uncontrolled responses… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Lin, A. A. (2009). The CD4+ T cell response to CNS viral infection. (Thesis). University of Cincinnati. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3351992

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):

Lin, Adora A. “The CD4+ T cell response to CNS viral infection.” 2009. Thesis, University of Cincinnati. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3351992.

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

MLA Handbook (7th Edition):

Lin, Adora A. “The CD4+ T cell response to CNS viral infection.” 2009. Web. 02 Apr 2020.

Vancouver:

Lin AA. The CD4+ T cell response to CNS viral infection. [Internet] [Thesis]. University of Cincinnati; 2009. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3351992.

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

Council of Science Editors:

Lin AA. The CD4+ T cell response to CNS viral infection. [Thesis]. University of Cincinnati; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3351992

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


University of California, Irvine

6. Pone, Egest. The role of Toll-like receptors and 14-3-3 proteins in the induction and targeting of immunoglobulin class switch DNA recombination.

Degree: 2009, University of California, Irvine

  We investigated the roles that Toll-like receptors (TLRs) play in B cell activation, immunoglobulin (Ig) class switch DNA recombination (CSR) and plasma cell formation,… (more)

Subjects/Keywords: Health Sciences; Immunology

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

APA (6th Edition):

Pone, E. (2009). The role of Toll-like receptors and 14-3-3 proteins in the induction and targeting of immunoglobulin class switch DNA recombination. (Thesis). University of California, Irvine. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3365707

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):

Pone, Egest. “The role of Toll-like receptors and 14-3-3 proteins in the induction and targeting of immunoglobulin class switch DNA recombination.” 2009. Thesis, University of California, Irvine. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3365707.

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

MLA Handbook (7th Edition):

Pone, Egest. “The role of Toll-like receptors and 14-3-3 proteins in the induction and targeting of immunoglobulin class switch DNA recombination.” 2009. Web. 02 Apr 2020.

Vancouver:

Pone E. The role of Toll-like receptors and 14-3-3 proteins in the induction and targeting of immunoglobulin class switch DNA recombination. [Internet] [Thesis]. University of California, Irvine; 2009. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3365707.

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

Council of Science Editors:

Pone E. The role of Toll-like receptors and 14-3-3 proteins in the induction and targeting of immunoglobulin class switch DNA recombination. [Thesis]. University of California, Irvine; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3365707

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

7. Wang, Yin. Host response to chlamydial urethral infection in male guinea pigs.

Degree: 2010, University of Arkansas for Medical Sciences

  Despite the high prevalence of chlamydia in men, there is very little known about the host response to chlamydial genital infection in the males;… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Wang, Y. (2010). Host response to chlamydial urethral infection in male guinea pigs. (Thesis). University of Arkansas for Medical Sciences. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3392184

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):

Wang, Yin. “Host response to chlamydial urethral infection in male guinea pigs.” 2010. Thesis, University of Arkansas for Medical Sciences. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3392184.

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

MLA Handbook (7th Edition):

Wang, Yin. “Host response to chlamydial urethral infection in male guinea pigs.” 2010. Web. 02 Apr 2020.

Vancouver:

Wang Y. Host response to chlamydial urethral infection in male guinea pigs. [Internet] [Thesis]. University of Arkansas for Medical Sciences; 2010. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3392184.

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

Council of Science Editors:

Wang Y. Host response to chlamydial urethral infection in male guinea pigs. [Thesis]. University of Arkansas for Medical Sciences; 2010. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3392184

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

8. Savage, Adam K. PLZF drives the innate-like effector program of NKT cells.

Degree: 2010, The University of Chicago

  Lineage fate decisions in hematopoietic development have been shown to rely on the activity of signature transcription factors such as Th-POK, T-bet, Foxp3, and… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Savage, A. K. (2010). PLZF drives the innate-like effector program of NKT cells. (Thesis). The University of Chicago. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3397294

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):

Savage, Adam K. “PLZF drives the innate-like effector program of NKT cells.” 2010. Thesis, The University of Chicago. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3397294.

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

MLA Handbook (7th Edition):

Savage, Adam K. “PLZF drives the innate-like effector program of NKT cells.” 2010. Web. 02 Apr 2020.

Vancouver:

Savage AK. PLZF drives the innate-like effector program of NKT cells. [Internet] [Thesis]. The University of Chicago; 2010. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3397294.

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

Council of Science Editors:

Savage AK. PLZF drives the innate-like effector program of NKT cells. [Thesis]. The University of Chicago; 2010. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3397294

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

9. Czura, Christopher Jordan. Neural regulation of inflammation and bleeding.

Degree: 2010, State University of New York at Stony Brook

  Recent advances in the field of immunology have revealed an unexpected role for the autonomic nervous system, specifically the vagus nerve, in controlling challenges… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Czura, C. J. (2010). Neural regulation of inflammation and bleeding. (Thesis). State University of New York at Stony Brook. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3401699

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):

Czura, Christopher Jordan. “Neural regulation of inflammation and bleeding.” 2010. Thesis, State University of New York at Stony Brook. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3401699.

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

MLA Handbook (7th Edition):

Czura, Christopher Jordan. “Neural regulation of inflammation and bleeding.” 2010. Web. 02 Apr 2020.

Vancouver:

Czura CJ. Neural regulation of inflammation and bleeding. [Internet] [Thesis]. State University of New York at Stony Brook; 2010. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3401699.

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

Council of Science Editors:

Czura CJ. Neural regulation of inflammation and bleeding. [Thesis]. State University of New York at Stony Brook; 2010. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3401699

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


Indiana University

10. Goswami, Ritobrata. Transcription factors in the development of Th9 cells.

Degree: 2013, Indiana University

  Cytokines are extracellular proteins that mediate communication between cells. T helper cell subsets secrete specific cytokines that promote the development of inflammation. Naïve CD4+… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Goswami, R. (2013). Transcription factors in the development of Th9 cells. (Thesis). Indiana University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3552581

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):

Goswami, Ritobrata. “Transcription factors in the development of Th9 cells.” 2013. Thesis, Indiana University. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3552581.

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

MLA Handbook (7th Edition):

Goswami, Ritobrata. “Transcription factors in the development of Th9 cells.” 2013. Web. 02 Apr 2020.

Vancouver:

Goswami R. Transcription factors in the development of Th9 cells. [Internet] [Thesis]. Indiana University; 2013. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3552581.

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

Council of Science Editors:

Goswami R. Transcription factors in the development of Th9 cells. [Thesis]. Indiana University; 2013. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3552581

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

11. Wei, John. Immunomodulatory Effects of Soy Isoflavones Genistein and Daidzein.

Degree: 2011, Mount Sinai School of Medicine

  Soybeans are the most common source of isoflavones in human food, and have been shown to have anti-inflammatory and anti-oxidant properties. We hypothesize that… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Wei, J. (2011). Immunomodulatory Effects of Soy Isoflavones Genistein and Daidzein. (Thesis). Mount Sinai School of Medicine. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=1499962

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):

Wei, John. “Immunomodulatory Effects of Soy Isoflavones Genistein and Daidzein.” 2011. Thesis, Mount Sinai School of Medicine. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=1499962.

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

MLA Handbook (7th Edition):

Wei, John. “Immunomodulatory Effects of Soy Isoflavones Genistein and Daidzein.” 2011. Web. 02 Apr 2020.

Vancouver:

Wei J. Immunomodulatory Effects of Soy Isoflavones Genistein and Daidzein. [Internet] [Thesis]. Mount Sinai School of Medicine; 2011. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1499962.

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

Council of Science Editors:

Wei J. Immunomodulatory Effects of Soy Isoflavones Genistein and Daidzein. [Thesis]. Mount Sinai School of Medicine; 2011. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=1499962

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


University of South Florida

12. Wahle, Joseph A. Signaling in natural killer cells| SHIP, 2B4 and the kinome.

Degree: 2008, University of South Florida

  The NK cell is a large granular lymphocyte that plays a key role in protecting the body against numerous pathogens including parasites, intracellular bacteria,… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Wahle, J. A. (2008). Signaling in natural killer cells| SHIP, 2B4 and the kinome. (Thesis). University of South Florida. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3306843

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):

Wahle, Joseph A. “Signaling in natural killer cells| SHIP, 2B4 and the kinome.” 2008. Thesis, University of South Florida. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3306843.

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

MLA Handbook (7th Edition):

Wahle, Joseph A. “Signaling in natural killer cells| SHIP, 2B4 and the kinome.” 2008. Web. 02 Apr 2020.

Vancouver:

Wahle JA. Signaling in natural killer cells| SHIP, 2B4 and the kinome. [Internet] [Thesis]. University of South Florida; 2008. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3306843.

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

Council of Science Editors:

Wahle JA. Signaling in natural killer cells| SHIP, 2B4 and the kinome. [Thesis]. University of South Florida; 2008. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3306843

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

13. Axtell, Robert C. The role of CD5 in experimental autoimmune encephalitomyelitis.

Degree: 2008, The University of Alabama at Birmingham

  The regulation of activation, differentiation and persistence of effector T-cells are critical for the development of Experimental Autoimmune Encephalomyelitis (EAE), the animal model of… (more)

Subjects/Keywords: Health Sciences; Immunology

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

APA (6th Edition):

Axtell, R. C. (2008). The role of CD5 in experimental autoimmune encephalitomyelitis. (Thesis). The University of Alabama at Birmingham. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3286365

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):

Axtell, Robert C. “The role of CD5 in experimental autoimmune encephalitomyelitis.” 2008. Thesis, The University of Alabama at Birmingham. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3286365.

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

MLA Handbook (7th Edition):

Axtell, Robert C. “The role of CD5 in experimental autoimmune encephalitomyelitis.” 2008. Web. 02 Apr 2020.

Vancouver:

Axtell RC. The role of CD5 in experimental autoimmune encephalitomyelitis. [Internet] [Thesis]. The University of Alabama at Birmingham; 2008. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3286365.

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

Council of Science Editors:

Axtell RC. The role of CD5 in experimental autoimmune encephalitomyelitis. [Thesis]. The University of Alabama at Birmingham; 2008. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3286365

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


Stanford University

14. Kattah, Michael George. High-content protein arrays for characterizing immune responses and pathophysiology at the molecular level.

Degree: 2008, Stanford University

  Proteomics and genomics technologies offer tremendous promise for comprehensively characterizing immune responses as well as generating and testing new hypotheses related to pathophysiology and… (more)

Subjects/Keywords: Health Sciences; Immunology

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

APA (6th Edition):

Kattah, M. G. (2008). High-content protein arrays for characterizing immune responses and pathophysiology at the molecular level. (Thesis). Stanford University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3313820

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):

Kattah, Michael George. “High-content protein arrays for characterizing immune responses and pathophysiology at the molecular level.” 2008. Thesis, Stanford University. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3313820.

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

MLA Handbook (7th Edition):

Kattah, Michael George. “High-content protein arrays for characterizing immune responses and pathophysiology at the molecular level.” 2008. Web. 02 Apr 2020.

Vancouver:

Kattah MG. High-content protein arrays for characterizing immune responses and pathophysiology at the molecular level. [Internet] [Thesis]. Stanford University; 2008. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3313820.

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

Council of Science Editors:

Kattah MG. High-content protein arrays for characterizing immune responses and pathophysiology at the molecular level. [Thesis]. Stanford University; 2008. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3313820

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


Iowa State University

15. Henderson, Abigail Lynn. Provocateurs and triggers| Induction of antigen-specific responses to the colonic resident microbiota and susceptibility to colitis.

Degree: 2008, Iowa State University

  Inflammatory bowel disease (IBD) is a chronic inflammation of the gastrointestinal tract (GI) that develops in part as a result of an aberrant immune… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Henderson, A. L. (2008). Provocateurs and triggers| Induction of antigen-specific responses to the colonic resident microbiota and susceptibility to colitis. (Thesis). Iowa State University. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3316200

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

Chicago Manual of Style (16th Edition):

Henderson, Abigail Lynn. “Provocateurs and triggers| Induction of antigen-specific responses to the colonic resident microbiota and susceptibility to colitis.” 2008. Thesis, Iowa State University. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3316200.

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

MLA Handbook (7th Edition):

Henderson, Abigail Lynn. “Provocateurs and triggers| Induction of antigen-specific responses to the colonic resident microbiota and susceptibility to colitis.” 2008. Web. 02 Apr 2020.

Vancouver:

Henderson AL. Provocateurs and triggers| Induction of antigen-specific responses to the colonic resident microbiota and susceptibility to colitis. [Internet] [Thesis]. Iowa State University; 2008. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3316200.

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

Council of Science Editors:

Henderson AL. Provocateurs and triggers| Induction of antigen-specific responses to the colonic resident microbiota and susceptibility to colitis. [Thesis]. Iowa State University; 2008. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3316200

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


Temple University

16. Kang, Sun-ah. Apoptotic Cells, Anti-Phospholipid Antibodies, and Anti-Chromatin Antibodies in Autoimmunity.

Degree: PhD, 2008, Temple University

Microbiology and Immunology

Antiphospholipid antibodies (APAs) are detected in various autoimmune diseases, such as antiphospholipid syndrome (APS) and systemic lupus erythematosus. In addition to their… (more)

Subjects/Keywords: Health Sciences, Immunology

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APA (6th Edition):

Kang, S. (2008). Apoptotic Cells, Anti-Phospholipid Antibodies, and Anti-Chromatin Antibodies in Autoimmunity. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,15651

Chicago Manual of Style (16th Edition):

Kang, Sun-ah. “Apoptotic Cells, Anti-Phospholipid Antibodies, and Anti-Chromatin Antibodies in Autoimmunity.” 2008. Doctoral Dissertation, Temple University. Accessed April 02, 2020. http://digital.library.temple.edu/u?/p245801coll10,15651.

MLA Handbook (7th Edition):

Kang, Sun-ah. “Apoptotic Cells, Anti-Phospholipid Antibodies, and Anti-Chromatin Antibodies in Autoimmunity.” 2008. Web. 02 Apr 2020.

Vancouver:

Kang S. Apoptotic Cells, Anti-Phospholipid Antibodies, and Anti-Chromatin Antibodies in Autoimmunity. [Internet] [Doctoral dissertation]. Temple University; 2008. [cited 2020 Apr 02]. Available from: http://digital.library.temple.edu/u?/p245801coll10,15651.

Council of Science Editors:

Kang S. Apoptotic Cells, Anti-Phospholipid Antibodies, and Anti-Chromatin Antibodies in Autoimmunity. [Doctoral Dissertation]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,15651


Temple University

17. Vas, Jaya. REGULATORY ROLES FOR NATURAL KILLER T CELLS AND TOLL-LIKE RECEPTORS IN MERCURY-INDUCED AUTOIMMUNITY.

Degree: PhD, 2008, Temple University

Microbiology and Immunology

The development of autoimmune diseases is frequently linked to exposure to environmental factors such as chemicals, drugs or infections. In the experimental… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Vas, J. (2008). REGULATORY ROLES FOR NATURAL KILLER T CELLS AND TOLL-LIKE RECEPTORS IN MERCURY-INDUCED AUTOIMMUNITY. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,20283

Chicago Manual of Style (16th Edition):

Vas, Jaya. “REGULATORY ROLES FOR NATURAL KILLER T CELLS AND TOLL-LIKE RECEPTORS IN MERCURY-INDUCED AUTOIMMUNITY.” 2008. Doctoral Dissertation, Temple University. Accessed April 02, 2020. http://digital.library.temple.edu/u?/p245801coll10,20283.

MLA Handbook (7th Edition):

Vas, Jaya. “REGULATORY ROLES FOR NATURAL KILLER T CELLS AND TOLL-LIKE RECEPTORS IN MERCURY-INDUCED AUTOIMMUNITY.” 2008. Web. 02 Apr 2020.

Vancouver:

Vas J. REGULATORY ROLES FOR NATURAL KILLER T CELLS AND TOLL-LIKE RECEPTORS IN MERCURY-INDUCED AUTOIMMUNITY. [Internet] [Doctoral dissertation]. Temple University; 2008. [cited 2020 Apr 02]. Available from: http://digital.library.temple.edu/u?/p245801coll10,20283.

Council of Science Editors:

Vas J. REGULATORY ROLES FOR NATURAL KILLER T CELLS AND TOLL-LIKE RECEPTORS IN MERCURY-INDUCED AUTOIMMUNITY. [Doctoral Dissertation]. Temple University; 2008. Available from: http://digital.library.temple.edu/u?/p245801coll10,20283

18. Liu, Chaohong. Regulatory functions of the actin cytoskeleton in B cell receptor signaling.

Degree: 2013, University of Maryland, College Park

  The binding of antigen (Ag) to the B cell receptor (BCR) induces the activation of intracellular signaling and the reorganization of the actin cytoskeleton.… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Liu, C. (2013). Regulatory functions of the actin cytoskeleton in B cell receptor signaling. (Thesis). University of Maryland, College Park. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3599621

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

Chicago Manual of Style (16th Edition):

Liu, Chaohong. “Regulatory functions of the actin cytoskeleton in B cell receptor signaling.” 2013. Thesis, University of Maryland, College Park. Accessed April 02, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3599621.

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

MLA Handbook (7th Edition):

Liu, Chaohong. “Regulatory functions of the actin cytoskeleton in B cell receptor signaling.” 2013. Web. 02 Apr 2020.

Vancouver:

Liu C. Regulatory functions of the actin cytoskeleton in B cell receptor signaling. [Internet] [Thesis]. University of Maryland, College Park; 2013. [cited 2020 Apr 02]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3599621.

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

Council of Science Editors:

Liu C. Regulatory functions of the actin cytoskeleton in B cell receptor signaling. [Thesis]. University of Maryland, College Park; 2013. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3599621

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


University of Cincinnati

19. SEXTON, STEPHANIE A. PREVALENCE AND IMPLEMENTATION OF ALLERGEN AVOIDANCE METHODS IN HOMES OF INFANTS AT HIGH RISK FOR ALLERGIC DISORDERS.

Degree: MS, Medicine : Epidemiology (Environmental Health), 2007, University of Cincinnati

 Background. Individuals suffering from allergic disorders may be able to reduce symptoms by reducing their environmental exposures. Objective. (1) Determine use of allergen avoidance methods… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

SEXTON, S. A. (2007). PREVALENCE AND IMPLEMENTATION OF ALLERGEN AVOIDANCE METHODS IN HOMES OF INFANTS AT HIGH RISK FOR ALLERGIC DISORDERS. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179315851

Chicago Manual of Style (16th Edition):

SEXTON, STEPHANIE A. “PREVALENCE AND IMPLEMENTATION OF ALLERGEN AVOIDANCE METHODS IN HOMES OF INFANTS AT HIGH RISK FOR ALLERGIC DISORDERS.” 2007. Masters Thesis, University of Cincinnati. Accessed April 02, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179315851.

MLA Handbook (7th Edition):

SEXTON, STEPHANIE A. “PREVALENCE AND IMPLEMENTATION OF ALLERGEN AVOIDANCE METHODS IN HOMES OF INFANTS AT HIGH RISK FOR ALLERGIC DISORDERS.” 2007. Web. 02 Apr 2020.

Vancouver:

SEXTON SA. PREVALENCE AND IMPLEMENTATION OF ALLERGEN AVOIDANCE METHODS IN HOMES OF INFANTS AT HIGH RISK FOR ALLERGIC DISORDERS. [Internet] [Masters thesis]. University of Cincinnati; 2007. [cited 2020 Apr 02]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179315851.

Council of Science Editors:

SEXTON SA. PREVALENCE AND IMPLEMENTATION OF ALLERGEN AVOIDANCE METHODS IN HOMES OF INFANTS AT HIGH RISK FOR ALLERGIC DISORDERS. [Masters Thesis]. University of Cincinnati; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179315851


Harvard University

20. Beyaz, Semir. Epigenetic Regulation of Cell Fate.

Degree: 2017, Harvard University

 A fundamental question in biology is to decipher how the same genomic information in an organism can give rise to diverse cellular states that are… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Beyaz, S. (2017). Epigenetic Regulation of Cell Fate. (Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945008

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):

Beyaz, Semir. “Epigenetic Regulation of Cell Fate.” 2017. Thesis, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945008.

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

MLA Handbook (7th Edition):

Beyaz, Semir. “Epigenetic Regulation of Cell Fate.” 2017. Web. 02 Apr 2020.

Vancouver:

Beyaz S. Epigenetic Regulation of Cell Fate. [Internet] [Thesis]. Harvard University; 2017. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945008.

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

Council of Science Editors:

Beyaz S. Epigenetic Regulation of Cell Fate. [Thesis]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945008

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


Harvard University

21. Siddall, Nicolle M. Evaluation of a HSV-2 Therapeutic Candidate Vaccine, GEN-003, for the Production of Herpes Simplex Virus Type 1 (HSV-1) Neutralizing Antibodies in Seropositive Individuals.

Degree: 2018, Harvard University

Oral and genital herpes diseases are major global health problems, infecting approximately 90% of the world’s population. Herpes simplex virus type 2 (HSV-2) is the… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Siddall, N. M. (2018). Evaluation of a HSV-2 Therapeutic Candidate Vaccine, GEN-003, for the Production of Herpes Simplex Virus Type 1 (HSV-1) Neutralizing Antibodies in Seropositive Individuals. (Thesis). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945098

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):

Siddall, Nicolle M. “Evaluation of a HSV-2 Therapeutic Candidate Vaccine, GEN-003, for the Production of Herpes Simplex Virus Type 1 (HSV-1) Neutralizing Antibodies in Seropositive Individuals.” 2018. Thesis, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945098.

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

MLA Handbook (7th Edition):

Siddall, Nicolle M. “Evaluation of a HSV-2 Therapeutic Candidate Vaccine, GEN-003, for the Production of Herpes Simplex Virus Type 1 (HSV-1) Neutralizing Antibodies in Seropositive Individuals.” 2018. Web. 02 Apr 2020.

Vancouver:

Siddall NM. Evaluation of a HSV-2 Therapeutic Candidate Vaccine, GEN-003, for the Production of Herpes Simplex Virus Type 1 (HSV-1) Neutralizing Antibodies in Seropositive Individuals. [Internet] [Thesis]. Harvard University; 2018. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945098.

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

Council of Science Editors:

Siddall NM. Evaluation of a HSV-2 Therapeutic Candidate Vaccine, GEN-003, for the Production of Herpes Simplex Virus Type 1 (HSV-1) Neutralizing Antibodies in Seropositive Individuals. [Thesis]. Harvard University; 2018. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:37945098

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

22. Goyal, Girija. Novel Role of PPAR-Gamma in GM-CSF Induced Anti-Tumor Immunity.

Degree: PhD, 2015, Harvard University

 Granulocyte macrophage colony stimulating factor (GM-CSF) mediates context dependent anti- or pro-inflammatory functions through cells of the myeloid lineage. GM-CSF signaling induces the expression of… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Goyal, G. (2015). Novel Role of PPAR-Gamma in GM-CSF Induced Anti-Tumor Immunity. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:14226102

Chicago Manual of Style (16th Edition):

Goyal, Girija. “Novel Role of PPAR-Gamma in GM-CSF Induced Anti-Tumor Immunity.” 2015. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:14226102.

MLA Handbook (7th Edition):

Goyal, Girija. “Novel Role of PPAR-Gamma in GM-CSF Induced Anti-Tumor Immunity.” 2015. Web. 02 Apr 2020.

Vancouver:

Goyal G. Novel Role of PPAR-Gamma in GM-CSF Induced Anti-Tumor Immunity. [Internet] [Doctoral dissertation]. Harvard University; 2015. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:14226102.

Council of Science Editors:

Goyal G. Novel Role of PPAR-Gamma in GM-CSF Induced Anti-Tumor Immunity. [Doctoral Dissertation]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:14226102


Harvard University

23. Booty, Matthew Gregory. Regulation of Effector CD8+ T Cells During Mycobacterium Tuberculosis Infection.

Degree: PhD, 2015, Harvard University

Approximately one-third of the world’s population is currently infected with Mycobacterium tuberculosis (Mtb), the bacillus that causes tuberculosis. Globally, it is the second leading cause… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Booty, M. G. (2015). Regulation of Effector CD8+ T Cells During Mycobacterium Tuberculosis Infection. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:17465317

Chicago Manual of Style (16th Edition):

Booty, Matthew Gregory. “Regulation of Effector CD8+ T Cells During Mycobacterium Tuberculosis Infection.” 2015. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17465317.

MLA Handbook (7th Edition):

Booty, Matthew Gregory. “Regulation of Effector CD8+ T Cells During Mycobacterium Tuberculosis Infection.” 2015. Web. 02 Apr 2020.

Vancouver:

Booty MG. Regulation of Effector CD8+ T Cells During Mycobacterium Tuberculosis Infection. [Internet] [Doctoral dissertation]. Harvard University; 2015. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17465317.

Council of Science Editors:

Booty MG. Regulation of Effector CD8+ T Cells During Mycobacterium Tuberculosis Infection. [Doctoral Dissertation]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17465317


Harvard University

24. McArdel, Shannon. Immunoregulatory Roles of CD48 in Autoimmunity and Tolerance.

Degree: PhD, 2015, Harvard University

CD48 is an adhesion and costimulatory molecule expressed constitutively on nearly all hematopoietic cells. Via interactions with its ligand CD2, it contributes to synapse organization… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

McArdel, S. (2015). Immunoregulatory Roles of CD48 in Autoimmunity and Tolerance. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467326

Chicago Manual of Style (16th Edition):

McArdel, Shannon. “Immunoregulatory Roles of CD48 in Autoimmunity and Tolerance.” 2015. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467326.

MLA Handbook (7th Edition):

McArdel, Shannon. “Immunoregulatory Roles of CD48 in Autoimmunity and Tolerance.” 2015. Web. 02 Apr 2020.

Vancouver:

McArdel S. Immunoregulatory Roles of CD48 in Autoimmunity and Tolerance. [Internet] [Doctoral dissertation]. Harvard University; 2015. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467326.

Council of Science Editors:

McArdel S. Immunoregulatory Roles of CD48 in Autoimmunity and Tolerance. [Doctoral Dissertation]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467326


Harvard University

25. Huynh, Alexandria. Mechanisms of regulatory T cell lineage homeostasis and stability.

Degree: PhD, 2015, Harvard University

Defined by the transcription factor Foxp3, regulatory T cells (Tregs) are a lineage of CD4+ T lymphocytes critical for the maintenance of immune homeostasis and… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Huynh, A. (2015). Mechanisms of regulatory T cell lineage homeostasis and stability. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467375

Chicago Manual of Style (16th Edition):

Huynh, Alexandria. “Mechanisms of regulatory T cell lineage homeostasis and stability.” 2015. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467375.

MLA Handbook (7th Edition):

Huynh, Alexandria. “Mechanisms of regulatory T cell lineage homeostasis and stability.” 2015. Web. 02 Apr 2020.

Vancouver:

Huynh A. Mechanisms of regulatory T cell lineage homeostasis and stability. [Internet] [Doctoral dissertation]. Harvard University; 2015. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467375.

Council of Science Editors:

Huynh A. Mechanisms of regulatory T cell lineage homeostasis and stability. [Doctoral Dissertation]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:17467375


Harvard University

26. Sefik, Esen. Individual Microbes Shape Various Parts of the Immune System.

Degree: PhD, 2015, Harvard University

The gastrointestinal tract, home to a vast number of bacteria, requires finely-tuned regulatory and effector immune mechanisms to maintain homeostasis and tolerance. In a large-scale… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Sefik, E. (2015). Individual Microbes Shape Various Parts of the Immune System. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:23845459

Chicago Manual of Style (16th Edition):

Sefik, Esen. “Individual Microbes Shape Various Parts of the Immune System.” 2015. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:23845459.

MLA Handbook (7th Edition):

Sefik, Esen. “Individual Microbes Shape Various Parts of the Immune System.” 2015. Web. 02 Apr 2020.

Vancouver:

Sefik E. Individual Microbes Shape Various Parts of the Immune System. [Internet] [Doctoral dissertation]. Harvard University; 2015. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:23845459.

Council of Science Editors:

Sefik E. Individual Microbes Shape Various Parts of the Immune System. [Doctoral Dissertation]. Harvard University; 2015. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:23845459


Harvard University

27. Loughhead, Scott McNabb. Immune Surveillance by Effector and Memory CD8+ T Cells.

Degree: PhD, 2016, Harvard University

 During priming, CD8+ T cells integrate a plethora of signals that affect their differentiation into subsets of CD8+ T cells with distinct migratory properties and… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Loughhead, S. M. (2016). Immune Surveillance by Effector and Memory CD8+ T Cells. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718721

Chicago Manual of Style (16th Edition):

Loughhead, Scott McNabb. “Immune Surveillance by Effector and Memory CD8+ T Cells.” 2016. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718721.

MLA Handbook (7th Edition):

Loughhead, Scott McNabb. “Immune Surveillance by Effector and Memory CD8+ T Cells.” 2016. Web. 02 Apr 2020.

Vancouver:

Loughhead SM. Immune Surveillance by Effector and Memory CD8+ T Cells. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718721.

Council of Science Editors:

Loughhead SM. Immune Surveillance by Effector and Memory CD8+ T Cells. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:26718721


Harvard University

28. Dobbins, Jessica Wells. Signaling of the T Cell Costimulatory Receptor CD28: Regulation and Initiation.

Degree: PhD, 2016, Harvard University

T cells provide antigen-specific immunity to pathogens, but are also capable of inducing destructive autoimmunity when responding to self antigens. In order to achieve full… (more)

Subjects/Keywords: Health Sciences; Immunology

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APA (6th Edition):

Dobbins, J. W. (2016). Signaling of the T Cell Costimulatory Receptor CD28: Regulation and Initiation. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493494

Chicago Manual of Style (16th Edition):

Dobbins, Jessica Wells. “Signaling of the T Cell Costimulatory Receptor CD28: Regulation and Initiation.” 2016. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493494.

MLA Handbook (7th Edition):

Dobbins, Jessica Wells. “Signaling of the T Cell Costimulatory Receptor CD28: Regulation and Initiation.” 2016. Web. 02 Apr 2020.

Vancouver:

Dobbins JW. Signaling of the T Cell Costimulatory Receptor CD28: Regulation and Initiation. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493494.

Council of Science Editors:

Dobbins JW. Signaling of the T Cell Costimulatory Receptor CD28: Regulation and Initiation. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493494


Harvard University

29. Suber, Freeman. Childhood Resistance to Influenza Mortality: Analysis in a Mouse Model.

Degree: PhD, 2016, Harvard University

During the 1918 influenza pandemic, children experienced significantly lower mortality compared to adults, with the onset of puberty marking a transition to greater disease susceptibility.… (more)

Subjects/Keywords: Health Sciences; Immunology

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

APA (6th Edition):

Suber, F. (2016). Childhood Resistance to Influenza Mortality: Analysis in a Mouse Model. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840685

Chicago Manual of Style (16th Edition):

Suber, Freeman. “Childhood Resistance to Influenza Mortality: Analysis in a Mouse Model.” 2016. Doctoral Dissertation, Harvard University. Accessed April 02, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840685.

MLA Handbook (7th Edition):

Suber, Freeman. “Childhood Resistance to Influenza Mortality: Analysis in a Mouse Model.” 2016. Web. 02 Apr 2020.

Vancouver:

Suber F. Childhood Resistance to Influenza Mortality: Analysis in a Mouse Model. [Internet] [Doctoral dissertation]. Harvard University; 2016. [cited 2020 Apr 02]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840685.

Council of Science Editors:

Suber F. Childhood Resistance to Influenza Mortality: Analysis in a Mouse Model. [Doctoral Dissertation]. Harvard University; 2016. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:33840685


McGill University

30. Tekkulru Srinivasa, Bharat. Changing concepts of Immunodeficiencies: primary immunodeficiencies in the adult.

Degree: MS, Department of Microbiology & Immunology, 2010, McGill University

Primary Immunodeficiencies (PIDs) are defined as inherent defects in the immune system. Over 200 PIDs have been described; many in recent years with improvements in… (more)

Subjects/Keywords: Health Sciences - Immunology

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

APA (6th Edition):

Tekkulru Srinivasa, B. (2010). Changing concepts of Immunodeficiencies: primary immunodeficiencies in the adult. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile95232.pdf

Chicago Manual of Style (16th Edition):

Tekkulru Srinivasa, Bharat. “Changing concepts of Immunodeficiencies: primary immunodeficiencies in the adult.” 2010. Masters Thesis, McGill University. Accessed April 02, 2020. http://digitool.library.mcgill.ca/thesisfile95232.pdf.

MLA Handbook (7th Edition):

Tekkulru Srinivasa, Bharat. “Changing concepts of Immunodeficiencies: primary immunodeficiencies in the adult.” 2010. Web. 02 Apr 2020.

Vancouver:

Tekkulru Srinivasa B. Changing concepts of Immunodeficiencies: primary immunodeficiencies in the adult. [Internet] [Masters thesis]. McGill University; 2010. [cited 2020 Apr 02]. Available from: http://digitool.library.mcgill.ca/thesisfile95232.pdf.

Council of Science Editors:

Tekkulru Srinivasa B. Changing concepts of Immunodeficiencies: primary immunodeficiencies in the adult. [Masters Thesis]. McGill University; 2010. Available from: http://digitool.library.mcgill.ca/thesisfile95232.pdf

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