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You searched for subject:(B cell). Showing records 1 – 30 of 649 total matches.

[1] [2] [3] [4] [5] … [22]

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University of Southern California

1. Nguyen, Quan T. Epigenetic control of B cell development by histone deubiquitinase Mysm1/2A-DUB.

Degree: MS, Molecular Microbiology & Immunology, 2012, University of Southern California

 The functions of many histone modification enzymes are unclear. Although their basic enzymatic functions have been described, the descriptions are often representative of a single… (more)

Subjects/Keywords: B cell development

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APA (6th Edition):

Nguyen, Q. T. (2012). Epigenetic control of B cell development by histone deubiquitinase Mysm1/2A-DUB. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384178/rec/2409

Chicago Manual of Style (16th Edition):

Nguyen, Quan T. “Epigenetic control of B cell development by histone deubiquitinase Mysm1/2A-DUB.” 2012. Masters Thesis, University of Southern California. Accessed August 20, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384178/rec/2409.

MLA Handbook (7th Edition):

Nguyen, Quan T. “Epigenetic control of B cell development by histone deubiquitinase Mysm1/2A-DUB.” 2012. Web. 20 Aug 2019.

Vancouver:

Nguyen QT. Epigenetic control of B cell development by histone deubiquitinase Mysm1/2A-DUB. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2019 Aug 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384178/rec/2409.

Council of Science Editors:

Nguyen QT. Epigenetic control of B cell development by histone deubiquitinase Mysm1/2A-DUB. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384178/rec/2409


University of New South Wales

2. Turner, Vivian. The functions of TRAF2, TRAF3 and cIAP1/cIAP2 in B cell biology.

Degree: Clinical School - St Vincent's Hospital, 2012, University of New South Wales

 TRAF2, TRAF3, cIAP1/cIAP2 act co-operatively as signal transduction proteins for members of the TNF receptor superfamily. This includes BAFF-R and CD40, key regulators of B(more)

Subjects/Keywords: cIAP; TRAF2; TRAF3; B cell

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APA (6th Edition):

Turner, V. (2012). The functions of TRAF2, TRAF3 and cIAP1/cIAP2 in B cell biology. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52161 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10831/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Turner, Vivian. “The functions of TRAF2, TRAF3 and cIAP1/cIAP2 in B cell biology.” 2012. Doctoral Dissertation, University of New South Wales. Accessed August 20, 2019. http://handle.unsw.edu.au/1959.4/52161 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10831/SOURCE01?view=true.

MLA Handbook (7th Edition):

Turner, Vivian. “The functions of TRAF2, TRAF3 and cIAP1/cIAP2 in B cell biology.” 2012. Web. 20 Aug 2019.

Vancouver:

Turner V. The functions of TRAF2, TRAF3 and cIAP1/cIAP2 in B cell biology. [Internet] [Doctoral dissertation]. University of New South Wales; 2012. [cited 2019 Aug 20]. Available from: http://handle.unsw.edu.au/1959.4/52161 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10831/SOURCE01?view=true.

Council of Science Editors:

Turner V. The functions of TRAF2, TRAF3 and cIAP1/cIAP2 in B cell biology. [Doctoral Dissertation]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52161 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10831/SOURCE01?view=true


University of Southern California

3. Liu, Jialuo. Physical activity and risk of B-cell non-Hodgkin's lymphoma among Los Angeles women.

Degree: MS, Applied Biostatistics and Epidemiology, 2012, University of Southern California

 Study Aim: There have been few studies focusing on the association between physical activity and risk of B-cell non-Hodgkin’s lymphomas (NHL) and their results are… (more)

Subjects/Keywords: physical activity; B-cell NHL

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APA (6th Edition):

Liu, J. (2012). Physical activity and risk of B-cell non-Hodgkin's lymphoma among Los Angeles women. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/217215/rec/5042

Chicago Manual of Style (16th Edition):

Liu, Jialuo. “Physical activity and risk of B-cell non-Hodgkin's lymphoma among Los Angeles women.” 2012. Masters Thesis, University of Southern California. Accessed August 20, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/217215/rec/5042.

MLA Handbook (7th Edition):

Liu, Jialuo. “Physical activity and risk of B-cell non-Hodgkin's lymphoma among Los Angeles women.” 2012. Web. 20 Aug 2019.

Vancouver:

Liu J. Physical activity and risk of B-cell non-Hodgkin's lymphoma among Los Angeles women. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2019 Aug 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/217215/rec/5042.

Council of Science Editors:

Liu J. Physical activity and risk of B-cell non-Hodgkin's lymphoma among Los Angeles women. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/217215/rec/5042


University of New South Wales

4. Berglund, Lucinda. The cytokine-mediated regulation of human B-cell differentiation.

Degree: Clinical School - St Vincent's Hospital, 2013, University of New South Wales

 The primary function of B cells is the secretion of antigen-specific antibody. The maturation of naïve B cells into plasmablasts capable of secreting high affinity… (more)

Subjects/Keywords: Cytokine; B cell; Plasmablast

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APA (6th Edition):

Berglund, L. (2013). The cytokine-mediated regulation of human B-cell differentiation. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53081 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11767/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Berglund, Lucinda. “The cytokine-mediated regulation of human B-cell differentiation.” 2013. Doctoral Dissertation, University of New South Wales. Accessed August 20, 2019. http://handle.unsw.edu.au/1959.4/53081 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11767/SOURCE01?view=true.

MLA Handbook (7th Edition):

Berglund, Lucinda. “The cytokine-mediated regulation of human B-cell differentiation.” 2013. Web. 20 Aug 2019.

Vancouver:

Berglund L. The cytokine-mediated regulation of human B-cell differentiation. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2019 Aug 20]. Available from: http://handle.unsw.edu.au/1959.4/53081 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11767/SOURCE01?view=true.

Council of Science Editors:

Berglund L. The cytokine-mediated regulation of human B-cell differentiation. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/53081 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11767/SOURCE01?view=true


University of Toronto

5. Ling, Alexanda Ka-Shing. The Role of BLNK in Avian B-cell Development.

Degree: 2013, University of Toronto

BLNK is an adaptor protein that functions in B-cell receptor signalling, and is vitally necessary at signalling checkpoints of mammalian B-cell development. However, its importance… (more)

Subjects/Keywords: B-cell development; BLNK; 0982

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APA (6th Edition):

Ling, A. K. (2013). The Role of BLNK in Avian B-cell Development. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43087

Chicago Manual of Style (16th Edition):

Ling, Alexanda Ka-Shing. “The Role of BLNK in Avian B-cell Development.” 2013. Masters Thesis, University of Toronto. Accessed August 20, 2019. http://hdl.handle.net/1807/43087.

MLA Handbook (7th Edition):

Ling, Alexanda Ka-Shing. “The Role of BLNK in Avian B-cell Development.” 2013. Web. 20 Aug 2019.

Vancouver:

Ling AK. The Role of BLNK in Avian B-cell Development. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1807/43087.

Council of Science Editors:

Ling AK. The Role of BLNK in Avian B-cell Development. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43087


University of Sydney

6. Guy, Thomas Victor. The roles of CD4 T cells and B cells in antitumour immunity .

Degree: 2016, University of Sydney

 There have been great advances in clinical immunotherapies against cancer over the past two decades. Most recently, immunotherapies directed against immuno-inhibitory molecules such as CTLA4… (more)

Subjects/Keywords: T cell; B cell; antibody; antitumour; immunity

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APA (6th Edition):

Guy, T. V. (2016). The roles of CD4 T cells and B cells in antitumour immunity . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/15427

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):

Guy, Thomas Victor. “The roles of CD4 T cells and B cells in antitumour immunity .” 2016. Thesis, University of Sydney. Accessed August 20, 2019. http://hdl.handle.net/2123/15427.

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

MLA Handbook (7th Edition):

Guy, Thomas Victor. “The roles of CD4 T cells and B cells in antitumour immunity .” 2016. Web. 20 Aug 2019.

Vancouver:

Guy TV. The roles of CD4 T cells and B cells in antitumour immunity . [Internet] [Thesis]. University of Sydney; 2016. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/2123/15427.

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

Council of Science Editors:

Guy TV. The roles of CD4 T cells and B cells in antitumour immunity . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/15427

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


University of Rochester

7. Garcia-Bates, Tatiana M. Regulation of normal and malignant B lineage cells by the peroxisome proliferator activated receptor gamma (PPARy) pathway.

Degree: PhD, 2009, University of Rochester

 Protective humoral immune responses depend on B lymphocyte clonal expansion and differentiation to generate plasma cells that produce high-affinity antibodies to fight infection. However, B(more)

Subjects/Keywords: PPAR Gamma; B Lymphoma; Multiple Myeloma; B Lymphocytes; B Cell Differentiation

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APA (6th Edition):

Garcia-Bates, T. M. (2009). Regulation of normal and malignant B lineage cells by the peroxisome proliferator activated receptor gamma (PPARy) pathway. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/8466

Chicago Manual of Style (16th Edition):

Garcia-Bates, Tatiana M. “Regulation of normal and malignant B lineage cells by the peroxisome proliferator activated receptor gamma (PPARy) pathway.” 2009. Doctoral Dissertation, University of Rochester. Accessed August 20, 2019. http://hdl.handle.net/1802/8466.

MLA Handbook (7th Edition):

Garcia-Bates, Tatiana M. “Regulation of normal and malignant B lineage cells by the peroxisome proliferator activated receptor gamma (PPARy) pathway.” 2009. Web. 20 Aug 2019.

Vancouver:

Garcia-Bates TM. Regulation of normal and malignant B lineage cells by the peroxisome proliferator activated receptor gamma (PPARy) pathway. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1802/8466.

Council of Science Editors:

Garcia-Bates TM. Regulation of normal and malignant B lineage cells by the peroxisome proliferator activated receptor gamma (PPARy) pathway. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/8466

8. Raman, Vanitha Sundaresa. Analysis of the regulation of B cell differentiation; -.

Degree: immunology, 2002, Jawaharlal Nehru University

none

Bibliography p.77-98

Advisors/Committee Members: George, Anna.

Subjects/Keywords: B cell; B cell differentiation

Page 1

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APA (6th Edition):

Raman, V. S. (2002). Analysis of the regulation of B cell differentiation; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/29184

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):

Raman, Vanitha Sundaresa. “Analysis of the regulation of B cell differentiation; -.” 2002. Thesis, Jawaharlal Nehru University. Accessed August 20, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/29184.

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

MLA Handbook (7th Edition):

Raman, Vanitha Sundaresa. “Analysis of the regulation of B cell differentiation; -.” 2002. Web. 20 Aug 2019.

Vancouver:

Raman VS. Analysis of the regulation of B cell differentiation; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2002. [cited 2019 Aug 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29184.

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

Council of Science Editors:

Raman VS. Analysis of the regulation of B cell differentiation; -. [Thesis]. Jawaharlal Nehru University; 2002. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29184

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


University of Louisville

9. Dascani, Paul Lorenzo. CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus.

Degree: PhD, 2018, University of Louisville

  Loss of function mutation in CD11b has been associated with incidence of systemic lupus erythematosus (SLE), a disease driven by B cell production of… (more)

Subjects/Keywords: B cell; systemic lupus erythematosus; CD11b; B cell receptor; Immunity

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APA (6th Edition):

Dascani, P. L. (2018). CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076

Chicago Manual of Style (16th Edition):

Dascani, Paul Lorenzo. “CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus.” 2018. Doctoral Dissertation, University of Louisville. Accessed August 20, 2019. 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076.

MLA Handbook (7th Edition):

Dascani, Paul Lorenzo. “CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus.” 2018. Web. 20 Aug 2019.

Vancouver:

Dascani PL. CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus. [Internet] [Doctoral dissertation]. University of Louisville; 2018. [cited 2019 Aug 20]. Available from: 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076.

Council of Science Editors:

Dascani PL. CD11b regulation of B cell receptor signaling in health and systemic lupus erythematosus. [Doctoral Dissertation]. University of Louisville; 2018. Available from: 10.18297/etd/3076 ; https://ir.library.louisville.edu/etd/3076


University of Minnesota

10. Rahe, Michael. The porcine memory B cell in conferring long term adaptive immunity to viral pathogens.

Degree: PhD, Comparative and Molecular Biosciences, 2017, University of Minnesota

 Porcine reproductive and respiratory syndrome virus (PRRSV) is the most important pathogen of swine health and well-being worldwide. Discovered nearly thirty years ago, there is… (more)

Subjects/Keywords: B cell; immunology; memory B cell; nsp7; PRRSV; tetramer

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APA (6th Edition):

Rahe, M. (2017). The porcine memory B cell in conferring long term adaptive immunity to viral pathogens. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/191463

Chicago Manual of Style (16th Edition):

Rahe, Michael. “The porcine memory B cell in conferring long term adaptive immunity to viral pathogens.” 2017. Doctoral Dissertation, University of Minnesota. Accessed August 20, 2019. http://hdl.handle.net/11299/191463.

MLA Handbook (7th Edition):

Rahe, Michael. “The porcine memory B cell in conferring long term adaptive immunity to viral pathogens.” 2017. Web. 20 Aug 2019.

Vancouver:

Rahe M. The porcine memory B cell in conferring long term adaptive immunity to viral pathogens. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/11299/191463.

Council of Science Editors:

Rahe M. The porcine memory B cell in conferring long term adaptive immunity to viral pathogens. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/191463


University of Rochester

11. Quach, Tam Dan. Human Anergic B Cells: IgMlo.

Degree: PhD, 2011, University of Rochester

B cell anergy represents an important mechanism of peripheral immunological tolerance which censors mature autoreactive B cells that escape central tolerance enforced by receptor editing… (more)

Subjects/Keywords: B Cell Anergy; Human Immunology; B Cell Tolerance

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APA (6th Edition):

Quach, T. D. (2011). Human Anergic B Cells: IgMlo. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/15857

Chicago Manual of Style (16th Edition):

Quach, Tam Dan. “Human Anergic B Cells: IgMlo.” 2011. Doctoral Dissertation, University of Rochester. Accessed August 20, 2019. http://hdl.handle.net/1802/15857.

MLA Handbook (7th Edition):

Quach, Tam Dan. “Human Anergic B Cells: IgMlo.” 2011. Web. 20 Aug 2019.

Vancouver:

Quach TD. Human Anergic B Cells: IgMlo. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1802/15857.

Council of Science Editors:

Quach TD. Human Anergic B Cells: IgMlo. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/15857


Duke University

12. Holl, Thomas Matthew. The Influence of B-cell Tolerance on Humoral Immunity to HIV-1 .

Degree: 2010, Duke University

  Several HIV-1 neutralizing antibodies (e.g. 2F5, 4E10) have been shown to react with self-antigens, suggesting that effective humoral responses to HIV-1 may be constrained… (more)

Subjects/Keywords: Health Sciences, Immunology; B cell; B-cell Development; B-cell Tolerance; HIV-1; Humoral Immunity; MPER

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APA (6th Edition):

Holl, T. M. (2010). The Influence of B-cell Tolerance on Humoral Immunity to HIV-1 . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/3053

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):

Holl, Thomas Matthew. “The Influence of B-cell Tolerance on Humoral Immunity to HIV-1 .” 2010. Thesis, Duke University. Accessed August 20, 2019. http://hdl.handle.net/10161/3053.

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

MLA Handbook (7th Edition):

Holl, Thomas Matthew. “The Influence of B-cell Tolerance on Humoral Immunity to HIV-1 .” 2010. Web. 20 Aug 2019.

Vancouver:

Holl TM. The Influence of B-cell Tolerance on Humoral Immunity to HIV-1 . [Internet] [Thesis]. Duke University; 2010. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/10161/3053.

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

Council of Science Editors:

Holl TM. The Influence of B-cell Tolerance on Humoral Immunity to HIV-1 . [Thesis]. Duke University; 2010. Available from: http://hdl.handle.net/10161/3053

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


Penn State University

13. Podolsky, Michael. Disparate Activation And Function of B Cells in Benign And Malignant Tumors of the Skin: Implications for Cancer Immunotherapy.

Degree: 2017, Penn State University

 The generation and progression of both benign and malignant cutaneous tumors is dependent upon initiating mutations in transformed keratinocytes, as well as supporting factors from… (more)

Subjects/Keywords: Squamous Cell Carcinoma; B-Cell; CD40; T-Cell; Ras; Immunotherapy

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APA (6th Edition):

Podolsky, M. (2017). Disparate Activation And Function of B Cells in Benign And Malignant Tumors of the Skin: Implications for Cancer Immunotherapy. (Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/13684map5535

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):

Podolsky, Michael. “Disparate Activation And Function of B Cells in Benign And Malignant Tumors of the Skin: Implications for Cancer Immunotherapy.” 2017. Thesis, Penn State University. Accessed August 20, 2019. https://etda.libraries.psu.edu/catalog/13684map5535.

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

MLA Handbook (7th Edition):

Podolsky, Michael. “Disparate Activation And Function of B Cells in Benign And Malignant Tumors of the Skin: Implications for Cancer Immunotherapy.” 2017. Web. 20 Aug 2019.

Vancouver:

Podolsky M. Disparate Activation And Function of B Cells in Benign And Malignant Tumors of the Skin: Implications for Cancer Immunotherapy. [Internet] [Thesis]. Penn State University; 2017. [cited 2019 Aug 20]. Available from: https://etda.libraries.psu.edu/catalog/13684map5535.

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

Council of Science Editors:

Podolsky M. Disparate Activation And Function of B Cells in Benign And Malignant Tumors of the Skin: Implications for Cancer Immunotherapy. [Thesis]. Penn State University; 2017. Available from: https://etda.libraries.psu.edu/catalog/13684map5535

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


University of Utah

14. Debnath, Irina. Defining the regluation of transitional B cell development and the expression of late transitional stage marker genes CD21 and CD23 by transcription factor networks and baff signaling.

Degree: PhD, Pathology;, 2010, University of Utah

 Transitional development of B cells starts when surface IgM expressing immature B cells from the bone marrow emigrate into the peripheral lymphoid organ spleen. These… (more)

Subjects/Keywords: B cell; CD21; CD23; Development; Transcription; Transitional

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APA (6th Edition):

Debnath, I. (2010). Defining the regluation of transitional B cell development and the expression of late transitional stage marker genes CD21 and CD23 by transcription factor networks and baff signaling. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/898/rec/286

Chicago Manual of Style (16th Edition):

Debnath, Irina. “Defining the regluation of transitional B cell development and the expression of late transitional stage marker genes CD21 and CD23 by transcription factor networks and baff signaling.” 2010. Doctoral Dissertation, University of Utah. Accessed August 20, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/898/rec/286.

MLA Handbook (7th Edition):

Debnath, Irina. “Defining the regluation of transitional B cell development and the expression of late transitional stage marker genes CD21 and CD23 by transcription factor networks and baff signaling.” 2010. Web. 20 Aug 2019.

Vancouver:

Debnath I. Defining the regluation of transitional B cell development and the expression of late transitional stage marker genes CD21 and CD23 by transcription factor networks and baff signaling. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2019 Aug 20]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/898/rec/286.

Council of Science Editors:

Debnath I. Defining the regluation of transitional B cell development and the expression of late transitional stage marker genes CD21 and CD23 by transcription factor networks and baff signaling. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/898/rec/286


Jawaharlal Nehru University

15. Chaudhari, Virendra Kumar. Regulation and Stability of the Intermediates in the B Cell signaling; -.

Degree: Genetic Engineering Biotechnology, 2009, Jawaharlal Nehru University

None

Bibliography given

Subjects/Keywords: B-cell; signal

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APA (6th Edition):

Chaudhari, V. K. (2009). Regulation and Stability of the Intermediates in the B Cell signaling; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/35246

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):

Chaudhari, Virendra Kumar. “Regulation and Stability of the Intermediates in the B Cell signaling; -.” 2009. Thesis, Jawaharlal Nehru University. Accessed August 20, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/35246.

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

MLA Handbook (7th Edition):

Chaudhari, Virendra Kumar. “Regulation and Stability of the Intermediates in the B Cell signaling; -.” 2009. Web. 20 Aug 2019.

Vancouver:

Chaudhari VK. Regulation and Stability of the Intermediates in the B Cell signaling; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2009. [cited 2019 Aug 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35246.

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

Council of Science Editors:

Chaudhari VK. Regulation and Stability of the Intermediates in the B Cell signaling; -. [Thesis]. Jawaharlal Nehru University; 2009. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/35246

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


University of Cincinnati

16. Schweitzer, Brock L. Interplay of Ets Transcription Factors in the Regulation of B Cell Development.

Degree: PhD, Medicine : Molecular Genetics, Biochemistry, and Microbiology, 2007, University of Cincinnati

 Transcriptional regulation of B cell differentiation is a tightly regulated, ordered process. Expression of transcription factors during development allows for proper gene expression and cellular… (more)

Subjects/Keywords: transcription factors; B cell; immunoglobulins; PU.1

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APA (6th Edition):

Schweitzer, B. L. (2007). Interplay of Ets Transcription Factors in the Regulation of B Cell Development. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172693414

Chicago Manual of Style (16th Edition):

Schweitzer, Brock L. “Interplay of Ets Transcription Factors in the Regulation of B Cell Development.” 2007. Doctoral Dissertation, University of Cincinnati. Accessed August 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172693414.

MLA Handbook (7th Edition):

Schweitzer, Brock L. “Interplay of Ets Transcription Factors in the Regulation of B Cell Development.” 2007. Web. 20 Aug 2019.

Vancouver:

Schweitzer BL. Interplay of Ets Transcription Factors in the Regulation of B Cell Development. [Internet] [Doctoral dissertation]. University of Cincinnati; 2007. [cited 2019 Aug 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172693414.

Council of Science Editors:

Schweitzer BL. Interplay of Ets Transcription Factors in the Regulation of B Cell Development. [Doctoral Dissertation]. University of Cincinnati; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1172693414


University of Zambia

17. Nchimba, Lweendo. Prevalence of Hepatitis B and C in Sickle-Cell disease patients at University Teaching Hospital, Lusaka, Zambia .

Degree: 2015, University of Zambia

 Background: Sickle Cell Disease (SCD) is highly prevalent in Africans. The SCD trait is 18% in the general population in Zambia and University Teaching Hospital… (more)

Subjects/Keywords: Sickle-Cell Anemia; Hepatitis B; Hepatitis C

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APA (6th Edition):

Nchimba, L. (2015). Prevalence of Hepatitis B and C in Sickle-Cell disease patients at University Teaching Hospital, Lusaka, Zambia . (Thesis). University of Zambia. Retrieved from http://hdl.handle.net/123456789/3726

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):

Nchimba, Lweendo. “Prevalence of Hepatitis B and C in Sickle-Cell disease patients at University Teaching Hospital, Lusaka, Zambia .” 2015. Thesis, University of Zambia. Accessed August 20, 2019. http://hdl.handle.net/123456789/3726.

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

MLA Handbook (7th Edition):

Nchimba, Lweendo. “Prevalence of Hepatitis B and C in Sickle-Cell disease patients at University Teaching Hospital, Lusaka, Zambia .” 2015. Web. 20 Aug 2019.

Vancouver:

Nchimba L. Prevalence of Hepatitis B and C in Sickle-Cell disease patients at University Teaching Hospital, Lusaka, Zambia . [Internet] [Thesis]. University of Zambia; 2015. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/123456789/3726.

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

Council of Science Editors:

Nchimba L. Prevalence of Hepatitis B and C in Sickle-Cell disease patients at University Teaching Hospital, Lusaka, Zambia . [Thesis]. University of Zambia; 2015. Available from: http://hdl.handle.net/123456789/3726

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


Boston College

18. Argueta, Shannon A. The Nutrients L-Glutamine and Glucose Have Unique Roles in B Lymphocyte Growth and Proliferation Responses.

Degree: PhD, Biology, 2016, Boston College

B cell activation is an energetically demanding process during which B lymphocytes undergo reprogramming and shift from a resting state to a highly proliferative, metabolically… (more)

Subjects/Keywords: B cell; Glucose; Glutamine; Lymphocyte; Metabolism

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APA (6th Edition):

Argueta, S. A. (2016). The Nutrients L-Glutamine and Glucose Have Unique Roles in B Lymphocyte Growth and Proliferation Responses. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107246

Chicago Manual of Style (16th Edition):

Argueta, Shannon A. “The Nutrients L-Glutamine and Glucose Have Unique Roles in B Lymphocyte Growth and Proliferation Responses.” 2016. Doctoral Dissertation, Boston College. Accessed August 20, 2019. http://dlib.bc.edu/islandora/object/bc-ir:107246.

MLA Handbook (7th Edition):

Argueta, Shannon A. “The Nutrients L-Glutamine and Glucose Have Unique Roles in B Lymphocyte Growth and Proliferation Responses.” 2016. Web. 20 Aug 2019.

Vancouver:

Argueta SA. The Nutrients L-Glutamine and Glucose Have Unique Roles in B Lymphocyte Growth and Proliferation Responses. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2019 Aug 20]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107246.

Council of Science Editors:

Argueta SA. The Nutrients L-Glutamine and Glucose Have Unique Roles in B Lymphocyte Growth and Proliferation Responses. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107246


Drexel University

19. Schwartz, Gregory W. Diversity analysis of B cell receptors - novel tools for repertoire comparisons.

Degree: 2016, Drexel University

The adaptive immune system provides the body the ability to mount a targeted defense against pathogens. This process depends not on a single cell but… (more)

Subjects/Keywords: Biomedical engineering; B cells; Cell receptors

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APA (6th Edition):

Schwartz, G. W. (2016). Diversity analysis of B cell receptors - novel tools for repertoire comparisons. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:6774

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):

Schwartz, Gregory W. “Diversity analysis of B cell receptors - novel tools for repertoire comparisons.” 2016. Thesis, Drexel University. Accessed August 20, 2019. http://hdl.handle.net/1860/idea:6774.

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

MLA Handbook (7th Edition):

Schwartz, Gregory W. “Diversity analysis of B cell receptors - novel tools for repertoire comparisons.” 2016. Web. 20 Aug 2019.

Vancouver:

Schwartz GW. Diversity analysis of B cell receptors - novel tools for repertoire comparisons. [Internet] [Thesis]. Drexel University; 2016. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1860/idea:6774.

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

Council of Science Editors:

Schwartz GW. Diversity analysis of B cell receptors - novel tools for repertoire comparisons. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:6774

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


Drexel University

20. Zhang, Bochao. Tools for the analysis of B-cell clonal diversity in immune repertoires.

Degree: 2018, Drexel University

 The lymphocytes of an organism harbor a diverse collection or repertoire of antigen receptors (antibodies (Ab) on B cells and T cell receptors (TCR) on… (more)

Subjects/Keywords: Medical sciences; Immunology; Cell receptors; B cells

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APA (6th Edition):

Zhang, B. (2018). Tools for the analysis of B-cell clonal diversity in immune repertoires. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7716

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):

Zhang, Bochao. “Tools for the analysis of B-cell clonal diversity in immune repertoires.” 2018. Thesis, Drexel University. Accessed August 20, 2019. http://hdl.handle.net/1860/idea:7716.

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

MLA Handbook (7th Edition):

Zhang, Bochao. “Tools for the analysis of B-cell clonal diversity in immune repertoires.” 2018. Web. 20 Aug 2019.

Vancouver:

Zhang B. Tools for the analysis of B-cell clonal diversity in immune repertoires. [Internet] [Thesis]. Drexel University; 2018. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1860/idea:7716.

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

Council of Science Editors:

Zhang B. Tools for the analysis of B-cell clonal diversity in immune repertoires. [Thesis]. Drexel University; 2018. Available from: http://hdl.handle.net/1860/idea:7716

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


University of Cambridge

21. Mielczarek, Olga. Spatial organisation of the immunoglobulin heavy chain locus and inter-chromosomal gene networks driving B cell development .

Degree: 2018, University of Cambridge

B lymphocytes produce a wide array of antibodies to recognize a countless number of antigens. This highly diverse repertoire is produced during B cell development… (more)

Subjects/Keywords: B cell development; chromosome conformation; Igh locus

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APA (6th Edition):

Mielczarek, O. (2018). Spatial organisation of the immunoglobulin heavy chain locus and inter-chromosomal gene networks driving B cell development . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273740

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):

Mielczarek, Olga. “Spatial organisation of the immunoglobulin heavy chain locus and inter-chromosomal gene networks driving B cell development .” 2018. Thesis, University of Cambridge. Accessed August 20, 2019. https://www.repository.cam.ac.uk/handle/1810/273740.

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

MLA Handbook (7th Edition):

Mielczarek, Olga. “Spatial organisation of the immunoglobulin heavy chain locus and inter-chromosomal gene networks driving B cell development .” 2018. Web. 20 Aug 2019.

Vancouver:

Mielczarek O. Spatial organisation of the immunoglobulin heavy chain locus and inter-chromosomal gene networks driving B cell development . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Aug 20]. Available from: https://www.repository.cam.ac.uk/handle/1810/273740.

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

Council of Science Editors:

Mielczarek O. Spatial organisation of the immunoglobulin heavy chain locus and inter-chromosomal gene networks driving B cell development . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273740

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


University of Edinburgh

22. Tse, George Hondag. The role of B cells in a mouse model of renal transplantation.

Degree: PhD, 2016, University of Edinburgh

 Renal transplantation is the optimum treatment for end-stage renal failure. B cells have been identified in chronic allograft damage (CAD) and are associated with the… (more)

Subjects/Keywords: 617.4; renal transplant; B cell; chronic rejection

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APA (6th Edition):

Tse, G. H. (2016). The role of B cells in a mouse model of renal transplantation. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/23420

Chicago Manual of Style (16th Edition):

Tse, George Hondag. “The role of B cells in a mouse model of renal transplantation.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed August 20, 2019. http://hdl.handle.net/1842/23420.

MLA Handbook (7th Edition):

Tse, George Hondag. “The role of B cells in a mouse model of renal transplantation.” 2016. Web. 20 Aug 2019.

Vancouver:

Tse GH. The role of B cells in a mouse model of renal transplantation. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1842/23420.

Council of Science Editors:

Tse GH. The role of B cells in a mouse model of renal transplantation. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/23420


Virginia Commonwealth University

23. Sturgill, Jamie. B cell ADAM10 Activity is Increased by Kainate Receptor Activation: Potential Role of this Pathway in Th2 Immunity and Cancer.

Degree: PhD, Microbiology & Immunology, 2010, Virginia Commonwealth University

 CD23 has long been appreciated to be a natural, negative regulator of IgE synthesis. This understanding is due in part to animal models in which… (more)

Subjects/Keywords: B cell; ADAM10; Medicine and Health Sciences

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APA (6th Edition):

Sturgill, J. (2010). B cell ADAM10 Activity is Increased by Kainate Receptor Activation: Potential Role of this Pathway in Th2 Immunity and Cancer. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/142

Chicago Manual of Style (16th Edition):

Sturgill, Jamie. “B cell ADAM10 Activity is Increased by Kainate Receptor Activation: Potential Role of this Pathway in Th2 Immunity and Cancer.” 2010. Doctoral Dissertation, Virginia Commonwealth University. Accessed August 20, 2019. https://scholarscompass.vcu.edu/etd/142.

MLA Handbook (7th Edition):

Sturgill, Jamie. “B cell ADAM10 Activity is Increased by Kainate Receptor Activation: Potential Role of this Pathway in Th2 Immunity and Cancer.” 2010. Web. 20 Aug 2019.

Vancouver:

Sturgill J. B cell ADAM10 Activity is Increased by Kainate Receptor Activation: Potential Role of this Pathway in Th2 Immunity and Cancer. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2010. [cited 2019 Aug 20]. Available from: https://scholarscompass.vcu.edu/etd/142.

Council of Science Editors:

Sturgill J. B cell ADAM10 Activity is Increased by Kainate Receptor Activation: Potential Role of this Pathway in Th2 Immunity and Cancer. [Doctoral Dissertation]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/142


University of Toronto

24. Kraguljac, Alan P. Use of Phospho-flow Cytometry to Define Influence of High-Risk Genetic Abnormalities on Cytokine-responsiveness in Human B-cell Leukemia.

Degree: 2012, University of Toronto

B-cell acute lymphoblastic leukemia (B-ALL) represents a collection of diseases that are categorized into subtypes based on the presence of recurrent cytogenetic abnormalities. These abnormalities… (more)

Subjects/Keywords: Leukemia; Signaling; B cell; Cytokine; CRLF2; 0760

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APA (6th Edition):

Kraguljac, A. P. (2012). Use of Phospho-flow Cytometry to Define Influence of High-Risk Genetic Abnormalities on Cytokine-responsiveness in Human B-cell Leukemia. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33296

Chicago Manual of Style (16th Edition):

Kraguljac, Alan P. “Use of Phospho-flow Cytometry to Define Influence of High-Risk Genetic Abnormalities on Cytokine-responsiveness in Human B-cell Leukemia.” 2012. Masters Thesis, University of Toronto. Accessed August 20, 2019. http://hdl.handle.net/1807/33296.

MLA Handbook (7th Edition):

Kraguljac, Alan P. “Use of Phospho-flow Cytometry to Define Influence of High-Risk Genetic Abnormalities on Cytokine-responsiveness in Human B-cell Leukemia.” 2012. Web. 20 Aug 2019.

Vancouver:

Kraguljac AP. Use of Phospho-flow Cytometry to Define Influence of High-Risk Genetic Abnormalities on Cytokine-responsiveness in Human B-cell Leukemia. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1807/33296.

Council of Science Editors:

Kraguljac AP. Use of Phospho-flow Cytometry to Define Influence of High-Risk Genetic Abnormalities on Cytokine-responsiveness in Human B-cell Leukemia. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33296


University of Minnesota

25. Nanton, Minelva Romelia. Protective B cell responses during Salmonella infection.

Degree: PhD, 2013, University of Minnesota

 In this thesis, we aim to further define the protective role of B cells during Salmonella infection. Understanding how B cells contribute to protective immunity… (more)

Subjects/Keywords: B cell; Non typhoid Salmonella; Salmonella; Typhoid

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APA (6th Edition):

Nanton, M. R. (2013). Protective B cell responses during Salmonella infection. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/158984

Chicago Manual of Style (16th Edition):

Nanton, Minelva Romelia. “Protective B cell responses during Salmonella infection.” 2013. Doctoral Dissertation, University of Minnesota. Accessed August 20, 2019. http://purl.umn.edu/158984.

MLA Handbook (7th Edition):

Nanton, Minelva Romelia. “Protective B cell responses during Salmonella infection.” 2013. Web. 20 Aug 2019.

Vancouver:

Nanton MR. Protective B cell responses during Salmonella infection. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2019 Aug 20]. Available from: http://purl.umn.edu/158984.

Council of Science Editors:

Nanton MR. Protective B cell responses during Salmonella infection. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://purl.umn.edu/158984


University of Rochester

26. Li, Jie. The Non-Antibody Producing Role of B Cells in Inflammatory-Erosive Arthritis.

Degree: PhD, 2012, University of Rochester

B cell depletion therapy (BCDT) with anti-CD20 has emerged as an effective intervention for some rheumatoid arthritis (RA) patients who fail to respond to traditional… (more)

Subjects/Keywords: B Cell; Rheumatoid Arthritis; Lymphatic Drainage

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APA (6th Edition):

Li, J. (2012). The Non-Antibody Producing Role of B Cells in Inflammatory-Erosive Arthritis. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/21367

Chicago Manual of Style (16th Edition):

Li, Jie. “The Non-Antibody Producing Role of B Cells in Inflammatory-Erosive Arthritis.” 2012. Doctoral Dissertation, University of Rochester. Accessed August 20, 2019. http://hdl.handle.net/1802/21367.

MLA Handbook (7th Edition):

Li, Jie. “The Non-Antibody Producing Role of B Cells in Inflammatory-Erosive Arthritis.” 2012. Web. 20 Aug 2019.

Vancouver:

Li J. The Non-Antibody Producing Role of B Cells in Inflammatory-Erosive Arthritis. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1802/21367.

Council of Science Editors:

Li J. The Non-Antibody Producing Role of B Cells in Inflammatory-Erosive Arthritis. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/21367


University of Rochester

27. Ramon, Sesquile. The Effects of Specialized Proresolving Lipid Mediators on B Lymphocyte Function:Implications for B Cell Differentiation and Antibody Production.

Degree: PhD, 2013, University of Rochester

 Inflammation is a natural process classically characterized by heat, redness, swelling and pain. Chronic or uncontrolled inflammation can lead to loss of tissue function and… (more)

Subjects/Keywords: B Cell; Inflammation; Lipid Mediator; Antibody

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APA (6th Edition):

Ramon, S. (2013). The Effects of Specialized Proresolving Lipid Mediators on B Lymphocyte Function:Implications for B Cell Differentiation and Antibody Production. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27278

Chicago Manual of Style (16th Edition):

Ramon, Sesquile. “The Effects of Specialized Proresolving Lipid Mediators on B Lymphocyte Function:Implications for B Cell Differentiation and Antibody Production.” 2013. Doctoral Dissertation, University of Rochester. Accessed August 20, 2019. http://hdl.handle.net/1802/27278.

MLA Handbook (7th Edition):

Ramon, Sesquile. “The Effects of Specialized Proresolving Lipid Mediators on B Lymphocyte Function:Implications for B Cell Differentiation and Antibody Production.” 2013. Web. 20 Aug 2019.

Vancouver:

Ramon S. The Effects of Specialized Proresolving Lipid Mediators on B Lymphocyte Function:Implications for B Cell Differentiation and Antibody Production. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/1802/27278.

Council of Science Editors:

Ramon S. The Effects of Specialized Proresolving Lipid Mediators on B Lymphocyte Function:Implications for B Cell Differentiation and Antibody Production. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27278


Boston University

28. Sawatzki, Kaitlin Michele Robbins. Examination of the immunoglobulin repertoire before and after Anthrax Vaccine Adsorbed immunization.

Degree: PhD, Microbiology, 2017, Boston University

 Anthrax Vaccine Adsorbed (AVA) immunization protects against anthrax disease by eliciting a neutralizing antibody response. However, antigen-specific antibody concentrations are not observed in high quantities… (more)

Subjects/Keywords: Immunology; Antibody; B cell; Plasmablast; Sequencing; Vaccine

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APA (6th Edition):

Sawatzki, K. M. R. (2017). Examination of the immunoglobulin repertoire before and after Anthrax Vaccine Adsorbed immunization. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/26489

Chicago Manual of Style (16th Edition):

Sawatzki, Kaitlin Michele Robbins. “Examination of the immunoglobulin repertoire before and after Anthrax Vaccine Adsorbed immunization.” 2017. Doctoral Dissertation, Boston University. Accessed August 20, 2019. http://hdl.handle.net/2144/26489.

MLA Handbook (7th Edition):

Sawatzki, Kaitlin Michele Robbins. “Examination of the immunoglobulin repertoire before and after Anthrax Vaccine Adsorbed immunization.” 2017. Web. 20 Aug 2019.

Vancouver:

Sawatzki KMR. Examination of the immunoglobulin repertoire before and after Anthrax Vaccine Adsorbed immunization. [Internet] [Doctoral dissertation]. Boston University; 2017. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/2144/26489.

Council of Science Editors:

Sawatzki KMR. Examination of the immunoglobulin repertoire before and after Anthrax Vaccine Adsorbed immunization. [Doctoral Dissertation]. Boston University; 2017. Available from: http://hdl.handle.net/2144/26489


Victoria University of Wellington

29. Gordon-Schneider, Rosemary. The Influence of BCL6 on the WNT Pathway in Glioblastoma Therapy Resistance.

Degree: 2018, Victoria University of Wellington

 Glioblastoma is a devastating disease with a median survival of 18 months from diagnosis and a 5 years survival rate of only 10%. The gold… (more)

Subjects/Keywords: Glioblastoma; WNT; BCL6; B-Cell Lymphoma 6

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APA (6th Edition):

Gordon-Schneider, R. (2018). The Influence of BCL6 on the WNT Pathway in Glioblastoma Therapy Resistance. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8153

Chicago Manual of Style (16th Edition):

Gordon-Schneider, Rosemary. “The Influence of BCL6 on the WNT Pathway in Glioblastoma Therapy Resistance.” 2018. Masters Thesis, Victoria University of Wellington. Accessed August 20, 2019. http://hdl.handle.net/10063/8153.

MLA Handbook (7th Edition):

Gordon-Schneider, Rosemary. “The Influence of BCL6 on the WNT Pathway in Glioblastoma Therapy Resistance.” 2018. Web. 20 Aug 2019.

Vancouver:

Gordon-Schneider R. The Influence of BCL6 on the WNT Pathway in Glioblastoma Therapy Resistance. [Internet] [Masters thesis]. Victoria University of Wellington; 2018. [cited 2019 Aug 20]. Available from: http://hdl.handle.net/10063/8153.

Council of Science Editors:

Gordon-Schneider R. The Influence of BCL6 on the WNT Pathway in Glioblastoma Therapy Resistance. [Masters Thesis]. Victoria University of Wellington; 2018. Available from: http://hdl.handle.net/10063/8153


University of New South Wales

30. Chan, Tyani. An investigation of in vivo antigen-specific B cell responses.

Degree: Clinical School - St Vincent's Hospital, 2010, University of New South Wales

 To optimize the initial wave of antibody production against T-dependent antigens, primary B cell clones with the highest antigen affinity are selected to generate the… (more)

Subjects/Keywords: Antibody; Immunology; B cell; Germinal centre

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APA (6th Edition):

Chan, T. (2010). An investigation of in vivo antigen-specific B cell responses. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/45616 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8898/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Chan, Tyani. “An investigation of in vivo antigen-specific B cell responses.” 2010. Doctoral Dissertation, University of New South Wales. Accessed August 20, 2019. http://handle.unsw.edu.au/1959.4/45616 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8898/SOURCE02?view=true.

MLA Handbook (7th Edition):

Chan, Tyani. “An investigation of in vivo antigen-specific B cell responses.” 2010. Web. 20 Aug 2019.

Vancouver:

Chan T. An investigation of in vivo antigen-specific B cell responses. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Aug 20]. Available from: http://handle.unsw.edu.au/1959.4/45616 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8898/SOURCE02?view=true.

Council of Science Editors:

Chan T. An investigation of in vivo antigen-specific B cell responses. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/45616 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8898/SOURCE02?view=true

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