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You searched for subject:( B Lymphocyte Subsets immunology 60). Showing records 1 – 30 of 18637 total matches.

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1. Wang, John Hsien. Marginal zone B-cell precursors as cellular agents for type I IFN promoted antigen transport.

Degree: PhD, 2009, University of Alabama – Birmingham

Type I IFN is a known pro-inflammatory cytokine that is associated with the development of systemic lupus erythematosus (SLE). At the level of B-cell regulation,… (more)

Subjects/Keywords: Autoimmunity  – immunology<; br>; B-Lymphocyte Subsets  – immunology<; br>; Interferon Type I  – immunology<; br>; Spleen  – immunology<; br>; Stem Cells  – immunology

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APA (6th Edition):

Wang, J. H. (2009). Marginal zone B-cell precursors as cellular agents for type I IFN promoted antigen transport. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,764

Chicago Manual of Style (16th Edition):

Wang, John Hsien. “Marginal zone B-cell precursors as cellular agents for type I IFN promoted antigen transport.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,764.

MLA Handbook (7th Edition):

Wang, John Hsien. “Marginal zone B-cell precursors as cellular agents for type I IFN promoted antigen transport.” 2009. Web. 24 Aug 2019.

Vancouver:

Wang JH. Marginal zone B-cell precursors as cellular agents for type I IFN promoted antigen transport. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,764.

Council of Science Editors:

Wang JH. Marginal zone B-cell precursors as cellular agents for type I IFN promoted antigen transport. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,764

2. Foote, Jeremy B. Polysaccharide specific B cells: a study of their development and function.

Degree: PhD, 2009, University of Alabama – Birmingham

Polysaccharides are important structural components of bacterial capsule and cell walls. Polysaccharide-specific antibodies are an important component of serologic memory capable of protecting against infection… (more)

Subjects/Keywords: Antibodies, Bacterial<; br>; Antibody Specificity<; br>; B-Lymphocyte Subsets  – immunology<; br>; Dextrans  – immunology<; br>; Mice<; br>; Polysaccharides, Bacterial  – pharmacology

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APA (6th Edition):

Foote, J. B. (2009). Polysaccharide specific B cells: a study of their development and function. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,497

Chicago Manual of Style (16th Edition):

Foote, Jeremy B. “Polysaccharide specific B cells: a study of their development and function.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,497.

MLA Handbook (7th Edition):

Foote, Jeremy B. “Polysaccharide specific B cells: a study of their development and function.” 2009. Web. 24 Aug 2019.

Vancouver:

Foote JB. Polysaccharide specific B cells: a study of their development and function. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,497.

Council of Science Editors:

Foote JB. Polysaccharide specific B cells: a study of their development and function. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,497

3. Le, Thuc-vy L. (Thuc-vy Lam). B cell clonal abundance and madcam-1 mediate affinity maturation and fate of germinal center B cells.

Degree: PhD, 2007, University of Alabama – Birmingham

One primary distinction separating the innate and the adaptive branches of the immune system is the numbers of ways in which a cell can recognize… (more)

Subjects/Keywords: Antibodies, Monoclonal<; br>; B-Lymphocyte Subsets  – immunology<; br>; Cell Adhesion Molecules  – metabolism<; br>; Dendritic Cells  – chemistry<; br>; Germinal Center  – metabolism

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APA (6th Edition):

Le, T. L. (. L. (2007). B cell clonal abundance and madcam-1 mediate affinity maturation and fate of germinal center B cells. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,526

Chicago Manual of Style (16th Edition):

Le, Thuc-vy L (Thuc-vy Lam). “B cell clonal abundance and madcam-1 mediate affinity maturation and fate of germinal center B cells.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,526.

MLA Handbook (7th Edition):

Le, Thuc-vy L (Thuc-vy Lam). “B cell clonal abundance and madcam-1 mediate affinity maturation and fate of germinal center B cells.” 2007. Web. 24 Aug 2019.

Vancouver:

Le TL(L. B cell clonal abundance and madcam-1 mediate affinity maturation and fate of germinal center B cells. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,526.

Council of Science Editors:

Le TL(L. B cell clonal abundance and madcam-1 mediate affinity maturation and fate of germinal center B cells. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,526

4. Lee, Yun Kyung. Late developmental plasticity in the T helper 17 lineage.

Degree: PhD, 2009, University of Alabama – Birmingham

CD4 T cells are a principal component of the adaptive immune system that is required for the efficient elimination of foreign antigens, but dysregulated CD4… (more)

Subjects/Keywords: Cell Lineage  – immunology<; br>; Interleukin-17  – metabolism<; br>; T-Lymphocyte Subsets  – immunology<; br>; Th1 Cells  – immunology<; br>; Th2 Cells  – immunology<; br>; Transforming Growth Factor beta  – metabolism

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APA (6th Edition):

Lee, Y. K. (2009). Late developmental plasticity in the T helper 17 lineage. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,916

Chicago Manual of Style (16th Edition):

Lee, Yun Kyung. “Late developmental plasticity in the T helper 17 lineage.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,916.

MLA Handbook (7th Edition):

Lee, Yun Kyung. “Late developmental plasticity in the T helper 17 lineage.” 2009. Web. 24 Aug 2019.

Vancouver:

Lee YK. Late developmental plasticity in the T helper 17 lineage. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,916.

Council of Science Editors:

Lee YK. Late developmental plasticity in the T helper 17 lineage. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,916

5. Maynard, Craig Lueland. IL-10-competent regulatory T cells: development, phenotype and function.

Degree: PhD, 2007, University of Alabama – Birmingham

In order to avoid chronic cell activation and inflammation the immune system has developed numerous mechanisms that cooperate to induce and/or maintain what is known… (more)

Subjects/Keywords: Cell Differentiation  – immunology<; br>; Forkhead Transcription Factors  – immunology<; br>; Inflammation  – immunology<; br>; Interleukin-10  – metabolism<; br>; T-Lymphocyte Subsets  – cytology<; br>; Transforming Growth Factor beta

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APA (6th Edition):

Maynard, C. L. (2007). IL-10-competent regulatory T cells: development, phenotype and function. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,529

Chicago Manual of Style (16th Edition):

Maynard, Craig Lueland. “IL-10-competent regulatory T cells: development, phenotype and function.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,529.

MLA Handbook (7th Edition):

Maynard, Craig Lueland. “IL-10-competent regulatory T cells: development, phenotype and function.” 2007. Web. 24 Aug 2019.

Vancouver:

Maynard CL. IL-10-competent regulatory T cells: development, phenotype and function. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,529.

Council of Science Editors:

Maynard CL. IL-10-competent regulatory T cells: development, phenotype and function. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,529

6. Beck, Benjamin H. (Benjamin Hester). Immunotherapy of cancer employing γδ-T cells: a study examining their utility and feasibility.

Degree: PhD, 2009, University of Alabama – Birmingham

Unlike antigen-specific αβ-T cells, γδ-T cells can recognize and lyse cancerous cells rapidly upon encounter in a manner that does not require the recognition of… (more)

Subjects/Keywords: Adenocarcinoma  – therapy<; br>; Breast Neoplasms  – pathology<; br>; Immunotherapy, Adoptive<; br>; Mammary Neoplasms, Experimental  – therapy<; br>; Receptors, Antigen, T-Cell, gamma-delta  – immunology T-Lymphocyte Subsets  – transplantation

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APA (6th Edition):

Beck, B. H. (. H. (2009). Immunotherapy of cancer employing γδ-T cells: a study examining their utility and feasibility. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1087

Chicago Manual of Style (16th Edition):

Beck, Benjamin H (Benjamin Hester). “Immunotherapy of cancer employing γδ-T cells: a study examining their utility and feasibility.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1087.

MLA Handbook (7th Edition):

Beck, Benjamin H (Benjamin Hester). “Immunotherapy of cancer employing γδ-T cells: a study examining their utility and feasibility.” 2009. Web. 24 Aug 2019.

Vancouver:

Beck BH(H. Immunotherapy of cancer employing γδ-T cells: a study examining their utility and feasibility. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1087.

Council of Science Editors:

Beck BH(H. Immunotherapy of cancer employing γδ-T cells: a study examining their utility and feasibility. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1087

7. Liu, Jing. Regulation of VH replacement in human immature B cells by B cell receptor (BCR)-mediated signaling.

Degree: PhD, 2009, University of Alabama – Birmingham

VH replacement occurs through RAG-mediated secondary recombination to change unwanted IgH genes. In this dissertation, I focused on studying the molecular mechanism that regulates VH… (more)

Subjects/Keywords: B-Lymphocytes  – immunology<; br>; Gene Rearrangement, B-Lymphocyte, Heavy Chain<; br>; Immunoglobulin Heavy Chains  – genetics<; br>; Immunoglobulin Light Chains  – genetics<; br>; Precursor Cells, B-Lymphoid<; br>; Recombination, Genetic

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APA (6th Edition):

Liu, J. (2009). Regulation of VH replacement in human immature B cells by B cell receptor (BCR)-mediated signaling. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,648

Chicago Manual of Style (16th Edition):

Liu, Jing. “Regulation of VH replacement in human immature B cells by B cell receptor (BCR)-mediated signaling.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,648.

MLA Handbook (7th Edition):

Liu, Jing. “Regulation of VH replacement in human immature B cells by B cell receptor (BCR)-mediated signaling.” 2009. Web. 24 Aug 2019.

Vancouver:

Liu J. Regulation of VH replacement in human immature B cells by B cell receptor (BCR)-mediated signaling. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,648.

Council of Science Editors:

Liu J. Regulation of VH replacement in human immature B cells by B cell receptor (BCR)-mediated signaling. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,648

8. Fan, Run. The potential role of VH replacement in editing and generating autoreactive antibodies.

Degree: PhD, 2009, University of Alabama – Birmingham

VH replacement occurs through RAG-mediated secondary recombination between an upstream VH gene and an existing VHDJH joint. In the first part of this dissertation, we… (more)

Subjects/Keywords: Antibody Specificity  – immunology<; br>; Autoimmune Diseases  – genetics<; br>; Gene Rearrangement, B-Lymphocyte, Heavy Chain<; br>; Immunoglobulin Heavy Chains  – genetics<; br>; Immunoglobulin Variable Region  – genetics<; br>; Lupus Erythematosus, Systemic<; br>; Virus Diseases

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APA (6th Edition):

Fan, R. (2009). The potential role of VH replacement in editing and generating autoreactive antibodies. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,667

Chicago Manual of Style (16th Edition):

Fan, Run. “The potential role of VH replacement in editing and generating autoreactive antibodies.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,667.

MLA Handbook (7th Edition):

Fan, Run. “The potential role of VH replacement in editing and generating autoreactive antibodies.” 2009. Web. 24 Aug 2019.

Vancouver:

Fan R. The potential role of VH replacement in editing and generating autoreactive antibodies. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,667.

Council of Science Editors:

Fan R. The potential role of VH replacement in editing and generating autoreactive antibodies. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,667


Washington University in St. Louis

9. Miller, Brian. The Functions of Autophagy Genes in Lymphocytes and Osteoclasts.

Degree: PhD, Biology and Biomedical Sciences: Immunology, 2011, Washington University in St. Louis

 Macroautophagy: herein autophagy) is a process by which cells degrade long-lived proteins and organelles. The autophagy pathway and autophagy genes have been implicated in many… (more)

Subjects/Keywords: Immunology; Cellular Biology; Autophagy, B Lymphocyte, Osteoclast, T Lymphocyte

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APA (6th Edition):

Miller, B. (2011). The Functions of Autophagy Genes in Lymphocytes and Osteoclasts. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/245

Chicago Manual of Style (16th Edition):

Miller, Brian. “The Functions of Autophagy Genes in Lymphocytes and Osteoclasts.” 2011. Doctoral Dissertation, Washington University in St. Louis. Accessed August 24, 2019. https://openscholarship.wustl.edu/etd/245.

MLA Handbook (7th Edition):

Miller, Brian. “The Functions of Autophagy Genes in Lymphocytes and Osteoclasts.” 2011. Web. 24 Aug 2019.

Vancouver:

Miller B. The Functions of Autophagy Genes in Lymphocytes and Osteoclasts. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2011. [cited 2019 Aug 24]. Available from: https://openscholarship.wustl.edu/etd/245.

Council of Science Editors:

Miller B. The Functions of Autophagy Genes in Lymphocytes and Osteoclasts. [Doctoral Dissertation]. Washington University in St. Louis; 2011. Available from: https://openscholarship.wustl.edu/etd/245

10. Haga, Christopher L. Analysis of the role of FCRL5 and FIGLERs in B cell development, signaling and malignancy.

Degree: PhD, 2008, University of Alabama – Birmingham

The regulation of signaling and migration is critical to B lymphocyte development, activation, and proliferation. This dissertation reports a functional role for Fc receptor-like molecule… (more)

Subjects/Keywords: B-Lymphocytes  – immunology <; br>; Fibronectins  – genetics <; br>; Immunoglobulins  – genetics <; br>; Lymphocyte Activation  – immunology <; br>; Multigene Family <; br>; Proteins  – genetics <; br>; Protein Tyrosine Phosphatase, Non-Receptor Type 6  – metabolism <; br>; Receptors, Antigen, B-Cell  – metabolism <; br>; Receptors, Fc  – metabolism <; br>; Receptors, Interleukin-7  – genetics<; br>; Signal Transduction  – immunology

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APA (6th Edition):

Haga, C. L. (2008). Analysis of the role of FCRL5 and FIGLERs in B cell development, signaling and malignancy. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,291

Chicago Manual of Style (16th Edition):

Haga, Christopher L. “Analysis of the role of FCRL5 and FIGLERs in B cell development, signaling and malignancy.” 2008. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,291.

MLA Handbook (7th Edition):

Haga, Christopher L. “Analysis of the role of FCRL5 and FIGLERs in B cell development, signaling and malignancy.” 2008. Web. 24 Aug 2019.

Vancouver:

Haga CL. Analysis of the role of FCRL5 and FIGLERs in B cell development, signaling and malignancy. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2008. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,291.

Council of Science Editors:

Haga CL. Analysis of the role of FCRL5 and FIGLERs in B cell development, signaling and malignancy. [Doctoral Dissertation]. University of Alabama – Birmingham; 2008. Available from: http://contentdm.mhsl.uab.edu/u?/etd,291


University of Iowa

11. Ness, Kristin Jennifer. Cytokine requirements for the differentiation and expansion of Il-17a- and Il-22-producing human Vγ2vδ2 T cells.

Degree: PhD, Immunology, 2011, University of Iowa

  Human γδ T cells expressing the Vγ2Vδ2 T cell antigen receptor play important roles in immune responses to microbial pathogens by monitoring prenyl pyrophosphate… (more)

Subjects/Keywords: Cell Differentiation; Humans; Interleukin-17A; Interleukin-22; Receptors; Antigen; T-Cell; gamma-delta; T-Lymphocyte Subsets; Immunology of Infectious Disease

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APA (6th Edition):

Ness, K. J. (2011). Cytokine requirements for the differentiation and expansion of Il-17a- and Il-22-producing human Vγ2vδ2 T cells. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/2751

Chicago Manual of Style (16th Edition):

Ness, Kristin Jennifer. “Cytokine requirements for the differentiation and expansion of Il-17a- and Il-22-producing human Vγ2vδ2 T cells.” 2011. Doctoral Dissertation, University of Iowa. Accessed August 24, 2019. https://ir.uiowa.edu/etd/2751.

MLA Handbook (7th Edition):

Ness, Kristin Jennifer. “Cytokine requirements for the differentiation and expansion of Il-17a- and Il-22-producing human Vγ2vδ2 T cells.” 2011. Web. 24 Aug 2019.

Vancouver:

Ness KJ. Cytokine requirements for the differentiation and expansion of Il-17a- and Il-22-producing human Vγ2vδ2 T cells. [Internet] [Doctoral dissertation]. University of Iowa; 2011. [cited 2019 Aug 24]. Available from: https://ir.uiowa.edu/etd/2751.

Council of Science Editors:

Ness KJ. Cytokine requirements for the differentiation and expansion of Il-17a- and Il-22-producing human Vγ2vδ2 T cells. [Doctoral Dissertation]. University of Iowa; 2011. Available from: https://ir.uiowa.edu/etd/2751


University of Oxford

12. Cheng, Daian. An investigation into the biology and function of protein Icb-1.

Degree: PhD, 2013, University of Oxford

 In this thesis I describe an investigation into the function of the protein Icb-1, a homologue of Themis1 in B cells and monocytes. Themis1 is… (more)

Subjects/Keywords: 612.01575; Immunology; B lymphocyte; Icb-1; Themis2; Themis1; BCR signalling

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APA (6th Edition):

Cheng, D. (2013). An investigation into the biology and function of protein Icb-1. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e6be188d-3a6f-4e95-aa3a-6f319d791f8c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581294

Chicago Manual of Style (16th Edition):

Cheng, Daian. “An investigation into the biology and function of protein Icb-1.” 2013. Doctoral Dissertation, University of Oxford. Accessed August 24, 2019. http://ora.ox.ac.uk/objects/uuid:e6be188d-3a6f-4e95-aa3a-6f319d791f8c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581294.

MLA Handbook (7th Edition):

Cheng, Daian. “An investigation into the biology and function of protein Icb-1.” 2013. Web. 24 Aug 2019.

Vancouver:

Cheng D. An investigation into the biology and function of protein Icb-1. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Aug 24]. Available from: http://ora.ox.ac.uk/objects/uuid:e6be188d-3a6f-4e95-aa3a-6f319d791f8c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581294.

Council of Science Editors:

Cheng D. An investigation into the biology and function of protein Icb-1. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:e6be188d-3a6f-4e95-aa3a-6f319d791f8c ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581294


Duke University

13. Su, Kuei-Ying. Clonal Studies of Human B Cells .

Degree: 2015, Duke University

B lymphocytes are multifunctional and play important roles in both innate and adaptive immunity. The diverse roles of B cells can be attributed to… (more)

Subjects/Keywords: Immunology; Cellular biology; Antigen presentation; B lymphocyte; Human; Repertoire

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APA (6th Edition):

Su, K. (2015). Clonal Studies of Human B Cells . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/11328

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):

Su, Kuei-Ying. “Clonal Studies of Human B Cells .” 2015. Thesis, Duke University. Accessed August 24, 2019. http://hdl.handle.net/10161/11328.

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

MLA Handbook (7th Edition):

Su, Kuei-Ying. “Clonal Studies of Human B Cells .” 2015. Web. 24 Aug 2019.

Vancouver:

Su K. Clonal Studies of Human B Cells . [Internet] [Thesis]. Duke University; 2015. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/10161/11328.

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

Council of Science Editors:

Su K. Clonal Studies of Human B Cells . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/11328

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


University of Iowa

14. Buchta, Claire Marie. Mechanisms of TLR signaling and cooperation in B lymphocytes.

Degree: PhD, Immunology, 2014, University of Iowa

B lymphocytes play important roles in antibody production, cytokine production, and antigen presentation to T cells. Ligation of Toll-like receptors (TLRs) on B cells… (more)

Subjects/Keywords: B lymphocyte; Toll-like receptor; TRAF5; Immunology of Infectious Disease

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APA (6th Edition):

Buchta, C. M. (2014). Mechanisms of TLR signaling and cooperation in B lymphocytes. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4584

Chicago Manual of Style (16th Edition):

Buchta, Claire Marie. “Mechanisms of TLR signaling and cooperation in B lymphocytes.” 2014. Doctoral Dissertation, University of Iowa. Accessed August 24, 2019. https://ir.uiowa.edu/etd/4584.

MLA Handbook (7th Edition):

Buchta, Claire Marie. “Mechanisms of TLR signaling and cooperation in B lymphocytes.” 2014. Web. 24 Aug 2019.

Vancouver:

Buchta CM. Mechanisms of TLR signaling and cooperation in B lymphocytes. [Internet] [Doctoral dissertation]. University of Iowa; 2014. [cited 2019 Aug 24]. Available from: https://ir.uiowa.edu/etd/4584.

Council of Science Editors:

Buchta CM. Mechanisms of TLR signaling and cooperation in B lymphocytes. [Doctoral Dissertation]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/4584


University of New South Wales

15. Gardam, Sandra. Regulation of lymphocyte development and function by TRAF2 and TRAF3.

Degree: Clinical School - St Vincent's Hospital, 2008, University of New South Wales

 Tumour necrosis factor receptor (TNFR) family members are widely expressed in cells of the immune system and are essential for the development and function of… (more)

Subjects/Keywords: B lymphocyte; Immunology; Signalling; TRAF

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APA (6th Edition):

Gardam, S. (2008). Regulation of lymphocyte development and function by TRAF2 and TRAF3. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true

Chicago Manual of Style (16th Edition):

Gardam, Sandra. “Regulation of lymphocyte development and function by TRAF2 and TRAF3.” 2008. Doctoral Dissertation, University of New South Wales. Accessed August 24, 2019. http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true.

MLA Handbook (7th Edition):

Gardam, Sandra. “Regulation of lymphocyte development and function by TRAF2 and TRAF3.” 2008. Web. 24 Aug 2019.

Vancouver:

Gardam S. Regulation of lymphocyte development and function by TRAF2 and TRAF3. [Internet] [Doctoral dissertation]. University of New South Wales; 2008. [cited 2019 Aug 24]. Available from: http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true.

Council of Science Editors:

Gardam S. Regulation of lymphocyte development and function by TRAF2 and TRAF3. [Doctoral Dissertation]. University of New South Wales; 2008. Available from: http://handle.unsw.edu.au/1959.4/42104 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:3686/SOURCE2?view=true


University of California – San Francisco

16. Wheeler, Matthew Lewis. Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism.

Degree: Biomedical Sciences, 2013, University of California – San Francisco

 Recognition of cognate antigen by the B cell antigen receptor (BCR) is one of the primary events that ultimately facilitate the production of pathogen-specific antibodies… (more)

Subjects/Keywords: Immunology; antibody response; B cell receptor; B lymphocyte; diacylglycerol; reactive oxygen species; signal transduction

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APA (6th Edition):

Wheeler, M. L. (2013). Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/3657t2n7

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):

Wheeler, Matthew Lewis. “Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism.” 2013. Thesis, University of California – San Francisco. Accessed August 24, 2019. http://www.escholarship.org/uc/item/3657t2n7.

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

MLA Handbook (7th Edition):

Wheeler, Matthew Lewis. “Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism.” 2013. Web. 24 Aug 2019.

Vancouver:

Wheeler ML. Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2019 Aug 24]. Available from: http://www.escholarship.org/uc/item/3657t2n7.

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

Council of Science Editors:

Wheeler ML. Fine-tuning B cell antigen receptor signaling by reactive oxygen species and diacylglycerol metabolism. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/3657t2n7

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

17. Jackson, Tanisha Anne. The role of FC receptor-like 2 in B cell signaling.

Degree: PhD, 2010, University of Alabama – Birmingham

Fc receptor-like 2 (FCRL2) is a transmembrane protein with immunomodulatory potential that is preferentially expressed by memory B cells in humans. It has two consensus… (more)

Subjects/Keywords: B-Lymphocytes  – immunology<; br>; FCRL2 protein, human<; br>; Receptors, Fc  – Immunology<; br>; Signal Transduction  – immunology

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APA (6th Edition):

Jackson, T. A. (2010). The role of FC receptor-like 2 in B cell signaling. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,713

Chicago Manual of Style (16th Edition):

Jackson, Tanisha Anne. “The role of FC receptor-like 2 in B cell signaling.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,713.

MLA Handbook (7th Edition):

Jackson, Tanisha Anne. “The role of FC receptor-like 2 in B cell signaling.” 2010. Web. 24 Aug 2019.

Vancouver:

Jackson TA. The role of FC receptor-like 2 in B cell signaling. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,713.

Council of Science Editors:

Jackson TA. The role of FC receptor-like 2 in B cell signaling. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,713

18. Dugger, Kari J. Visualizing the function and migration of T cells.

Degree: PhD, 2007, University of Alabama – Birmingham

Lymphocytes are highly mobile cells that can travel throughout the body in response to a multitude of stimuli. Identifying lymphocyte trafficking patterns in vivo is… (more)

Subjects/Keywords: Antigens, CD <; br>; CD8-Positive T-Lymphocytes  – immunology <; br>; Encephalomyelitis, Autoimmune, Experimental  – immunology <; br>; Luciferases  – analysis <; br>; Lymphocyte Activation

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APA (6th Edition):

Dugger, K. J. (2007). Visualizing the function and migration of T cells. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,120

Chicago Manual of Style (16th Edition):

Dugger, Kari J. “Visualizing the function and migration of T cells.” 2007. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,120.

MLA Handbook (7th Edition):

Dugger, Kari J. “Visualizing the function and migration of T cells.” 2007. Web. 24 Aug 2019.

Vancouver:

Dugger KJ. Visualizing the function and migration of T cells. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2007. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,120.

Council of Science Editors:

Dugger KJ. Visualizing the function and migration of T cells. [Doctoral Dissertation]. University of Alabama – Birmingham; 2007. Available from: http://contentdm.mhsl.uab.edu/u?/etd,120

19. Akinsiku, Olusimidele Tolulope. Qualitative analysis of HIV-1-specific CD8 T cell responses.

Degree: PhD, 2011, University of Alabama – Birmingham

In the absence of antiretroviral therapy (ART), the majority of individuals infected with human immunodeficiency virus-1 (HIV-1) will develop AIDS. HIV-1-infected controllers are exceptions to… (more)

Subjects/Keywords: CD8-Positive T-Lymphocytes  – immunology<; br>; Epitopes, T-Lymphocyte  – immunology<; br>; HIV Infections  – immunology<; br>; HIV-1  – immunology<; br>; HIV-1  – physiology<; br>; Interleukin-2  – metabolism<; br>; RNA, Antisense  – immunology<; br>; RNA, Viral  – immunology<; br>; Transcription, Genetic  – immunology

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

APA (6th Edition):

Akinsiku, O. T. (2011). Qualitative analysis of HIV-1-specific CD8 T cell responses. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1148

Chicago Manual of Style (16th Edition):

Akinsiku, Olusimidele Tolulope. “Qualitative analysis of HIV-1-specific CD8 T cell responses.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1148.

MLA Handbook (7th Edition):

Akinsiku, Olusimidele Tolulope. “Qualitative analysis of HIV-1-specific CD8 T cell responses.” 2011. Web. 24 Aug 2019.

Vancouver:

Akinsiku OT. Qualitative analysis of HIV-1-specific CD8 T cell responses. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1148.

Council of Science Editors:

Akinsiku OT. Qualitative analysis of HIV-1-specific CD8 T cell responses. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1148

20. Chen, Yao, Ph.D. Cathelin-related antimicrobial peptide (CRAMP) regulates B cell IgG1 production.

Degree: PhD, 2010, University of Alabama – Birmingham

Mammalian antimicrobial peptides, including cathelicidins and defensins, play an important role in host defense via direct antimicrobial activity as well as immune regulation. The cathelin-related… (more)

Subjects/Keywords: Antibody Formation  – immunology<; br>; Anti-Bacterial Agents  – chemistry<; br>; B-Lymphocytes  – immunology<; br>; Cathelicidins  – immunology<; br>; Immunoglobulin G.<; br>; Mice

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APA (6th Edition):

Chen, Yao, P. D. (2010). Cathelin-related antimicrobial peptide (CRAMP) regulates B cell IgG1 production. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,701

Chicago Manual of Style (16th Edition):

Chen, Yao, Ph D. “Cathelin-related antimicrobial peptide (CRAMP) regulates B cell IgG1 production.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,701.

MLA Handbook (7th Edition):

Chen, Yao, Ph D. “Cathelin-related antimicrobial peptide (CRAMP) regulates B cell IgG1 production.” 2010. Web. 24 Aug 2019.

Vancouver:

Chen, Yao PD. Cathelin-related antimicrobial peptide (CRAMP) regulates B cell IgG1 production. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,701.

Council of Science Editors:

Chen, Yao PD. Cathelin-related antimicrobial peptide (CRAMP) regulates B cell IgG1 production. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,701


Boston University

21. Bootwala, Ali Habib. L2pB1 cells are essential for the inhibition of 3D tumor spheroids by syngeneic peritoneal immune cells.

Degree: MS, Medical Sciences, 2019, Boston University

 INTRODUCTION: Programmed Death Ligand 2 positive B1 cells (L2pB1) cells have a unique immunoglobulin repertoire that is poly-reactive to self-antigens and have previously been shown… (more)

Subjects/Keywords: Immunology; 3D tumor spheroid; B1a cell; B lymphocyte; L2pB1; PD-L2; Programmed death ligand 2

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APA (6th Edition):

Bootwala, A. H. (2019). L2pB1 cells are essential for the inhibition of 3D tumor spheroids by syngeneic peritoneal immune cells. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/34840

Chicago Manual of Style (16th Edition):

Bootwala, Ali Habib. “L2pB1 cells are essential for the inhibition of 3D tumor spheroids by syngeneic peritoneal immune cells.” 2019. Masters Thesis, Boston University. Accessed August 24, 2019. http://hdl.handle.net/2144/34840.

MLA Handbook (7th Edition):

Bootwala, Ali Habib. “L2pB1 cells are essential for the inhibition of 3D tumor spheroids by syngeneic peritoneal immune cells.” 2019. Web. 24 Aug 2019.

Vancouver:

Bootwala AH. L2pB1 cells are essential for the inhibition of 3D tumor spheroids by syngeneic peritoneal immune cells. [Internet] [Masters thesis]. Boston University; 2019. [cited 2019 Aug 24]. Available from: http://hdl.handle.net/2144/34840.

Council of Science Editors:

Bootwala AH. L2pB1 cells are essential for the inhibition of 3D tumor spheroids by syngeneic peritoneal immune cells. [Masters Thesis]. Boston University; 2019. Available from: http://hdl.handle.net/2144/34840

22. Chen, Alex T. Regulation of Immune Pathogenesis by Antigen-Specific CD8 T Cells Following Sequential Heterologous Infections: A Dissertation.

Degree: Immunology and Microbiology, Pathology, 2010, U of Massachusetts : Med

  Previously, our lab demonstrated that heterologous immunity could result in either gain or loss of protective immunity and alteration in immune pathology following infection… (more)

Subjects/Keywords: CD8-Positive T-Lymphocytes; Immune System; Immunity; Immunologic Memory; T-Lymphocyte Subsets; Lymphocytic choriomeningitis virus; Pichinde virus; Cells; Hemic and Immune Systems; Immunology and Infectious Disease; Pathology; Viruses

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

APA (6th Edition):

Chen, A. T. (2010). Regulation of Immune Pathogenesis by Antigen-Specific CD8 T Cells Following Sequential Heterologous Infections: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/489

Chicago Manual of Style (16th Edition):

Chen, Alex T. “Regulation of Immune Pathogenesis by Antigen-Specific CD8 T Cells Following Sequential Heterologous Infections: A Dissertation.” 2010. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 24, 2019. https://escholarship.umassmed.edu/gsbs_diss/489.

MLA Handbook (7th Edition):

Chen, Alex T. “Regulation of Immune Pathogenesis by Antigen-Specific CD8 T Cells Following Sequential Heterologous Infections: A Dissertation.” 2010. Web. 24 Aug 2019.

Vancouver:

Chen AT. Regulation of Immune Pathogenesis by Antigen-Specific CD8 T Cells Following Sequential Heterologous Infections: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2010. [cited 2019 Aug 24]. Available from: https://escholarship.umassmed.edu/gsbs_diss/489.

Council of Science Editors:

Chen AT. Regulation of Immune Pathogenesis by Antigen-Specific CD8 T Cells Following Sequential Heterologous Infections: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2010. Available from: https://escholarship.umassmed.edu/gsbs_diss/489

23. Narayan, Kavitha. The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation.

Degree: Immunology and Microbiology, Pathology, 2011, U of Massachusetts : Med

  The immune system generates discrete lineages of cells that are designed to respond optimally to environmental cues and infectious agents. Two distinct lineages of… (more)

Subjects/Keywords: Immunity; Innate; T-Lymphocytes; T-Lymphocyte Subsets; Genes; T-Cell Receptor; Cells; Genetic Phenomena; Hemic and Immune Systems; Immunology and Infectious Disease

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APA (6th Edition):

Narayan, K. (2011). The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/527

Chicago Manual of Style (16th Edition):

Narayan, Kavitha. “The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed August 24, 2019. https://escholarship.umassmed.edu/gsbs_diss/527.

MLA Handbook (7th Edition):

Narayan, Kavitha. “The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation.” 2011. Web. 24 Aug 2019.

Vancouver:

Narayan K. The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Aug 24]. Available from: https://escholarship.umassmed.edu/gsbs_diss/527.

Council of Science Editors:

Narayan K. The Function of Innate γδ T Cell Subsets is Molecularly Programmed in the Thymus in Three Stages: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/527

24. Cao, Shuwen. Cytokine Signaling In A Mouse Model Of Parkinson's Disease.

Degree: 2012, University of Alabama – Birmingham

The protein alpha-synuclein (α-SYN), which is found in the Lewy bodies of dopaminergic (DA) neurons in the substantia nigra (SN), has an important role in… (more)

Subjects/Keywords: alpha-Synuclein.<; br>; Brain – immunology.<; br>; Cytokines – metabolism<; br>; Gene Expression Regulation – drug effects<; br>; Immune System Processes – immunology.<; br>; Lymphocyte Activation – immunology<; br>; Microglia<; br>; Parkinson Disease – immunology.<; br>; Receptors, IgG – metabolism.<; br>; Signal Transduction – drug effects

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APA (6th Edition):

Cao, S. (2012). Cytokine Signaling In A Mouse Model Of Parkinson's Disease. (Thesis). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1796

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):

Cao, Shuwen. “Cytokine Signaling In A Mouse Model Of Parkinson's Disease.” 2012. Thesis, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1796.

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

MLA Handbook (7th Edition):

Cao, Shuwen. “Cytokine Signaling In A Mouse Model Of Parkinson's Disease.” 2012. Web. 24 Aug 2019.

Vancouver:

Cao S. Cytokine Signaling In A Mouse Model Of Parkinson's Disease. [Internet] [Thesis]. University of Alabama – Birmingham; 2012. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1796.

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

Council of Science Editors:

Cao S. Cytokine Signaling In A Mouse Model Of Parkinson's Disease. [Thesis]. University of Alabama – Birmingham; 2012. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1796

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

25. Hussein, Mourad. Caractérisation des mécanismes cellulaires, génétiques et épigénétiques de la différenciation terminale des lymphocytes B chez l’homme : Characterization of the cellular, genetic and epigenetic mechanisms of human terminal B cell differentiation.

Degree: Docteur es, Biologie, 2013, Rennes 1

Ces dernières années ont été marquées par une progression importante dans la connaissance de la physiologie des cellules B in vivo et de leur différenciation… (more)

Subjects/Keywords: Immunologie; Différenciation; Centre germinatif; Lymphocyte B; Plasmablastes; Méthylation; Aicda; Immunology; B cells; Differentiation; Germinal centers; Methylation

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APA (6th Edition):

Hussein, M. (2013). Caractérisation des mécanismes cellulaires, génétiques et épigénétiques de la différenciation terminale des lymphocytes B chez l’homme : Characterization of the cellular, genetic and epigenetic mechanisms of human terminal B cell differentiation. (Doctoral Dissertation). Rennes 1. Retrieved from http://www.theses.fr/2013REN1S198

Chicago Manual of Style (16th Edition):

Hussein, Mourad. “Caractérisation des mécanismes cellulaires, génétiques et épigénétiques de la différenciation terminale des lymphocytes B chez l’homme : Characterization of the cellular, genetic and epigenetic mechanisms of human terminal B cell differentiation.” 2013. Doctoral Dissertation, Rennes 1. Accessed August 24, 2019. http://www.theses.fr/2013REN1S198.

MLA Handbook (7th Edition):

Hussein, Mourad. “Caractérisation des mécanismes cellulaires, génétiques et épigénétiques de la différenciation terminale des lymphocytes B chez l’homme : Characterization of the cellular, genetic and epigenetic mechanisms of human terminal B cell differentiation.” 2013. Web. 24 Aug 2019.

Vancouver:

Hussein M. Caractérisation des mécanismes cellulaires, génétiques et épigénétiques de la différenciation terminale des lymphocytes B chez l’homme : Characterization of the cellular, genetic and epigenetic mechanisms of human terminal B cell differentiation. [Internet] [Doctoral dissertation]. Rennes 1; 2013. [cited 2019 Aug 24]. Available from: http://www.theses.fr/2013REN1S198.

Council of Science Editors:

Hussein M. Caractérisation des mécanismes cellulaires, génétiques et épigénétiques de la différenciation terminale des lymphocytes B chez l’homme : Characterization of the cellular, genetic and epigenetic mechanisms of human terminal B cell differentiation. [Doctoral Dissertation]. Rennes 1; 2013. Available from: http://www.theses.fr/2013REN1S198


McGill University

26. Williams, Julia Leigh. Evidence of a thymic abnormality in relapsing-remitting multiple sclerosis.

Degree: MS, Department of Pathology., 2008, McGill University

 The peripheral naive CD4 T cell pool is homeostatically regulated through a balance of thymic production, delivery of survival signals and homeostatic proliferation. CD4 recent… (more)

Subjects/Keywords: Multiple Sclerosis, Relapsing-Remitting  – immunology.; CD4-Positive T-Lymphocytes  – immunology.; T-Lymphocyte Subsets  – immunology.; Thymus Gland  – immunology.

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APA (6th Edition):

Williams, J. L. (2008). Evidence of a thymic abnormality in relapsing-remitting multiple sclerosis. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile111617.pdf

Chicago Manual of Style (16th Edition):

Williams, Julia Leigh. “Evidence of a thymic abnormality in relapsing-remitting multiple sclerosis.” 2008. Masters Thesis, McGill University. Accessed August 24, 2019. http://digitool.library.mcgill.ca/thesisfile111617.pdf.

MLA Handbook (7th Edition):

Williams, Julia Leigh. “Evidence of a thymic abnormality in relapsing-remitting multiple sclerosis.” 2008. Web. 24 Aug 2019.

Vancouver:

Williams JL. Evidence of a thymic abnormality in relapsing-remitting multiple sclerosis. [Internet] [Masters thesis]. McGill University; 2008. [cited 2019 Aug 24]. Available from: http://digitool.library.mcgill.ca/thesisfile111617.pdf.

Council of Science Editors:

Williams JL. Evidence of a thymic abnormality in relapsing-remitting multiple sclerosis. [Masters Thesis]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile111617.pdf


University of Pennsylvania

27. Geherin, Skye. Recirculation of Innate Lymphocyte Subsets in the Skin.

Degree: 2014, University of Pennsylvania

 The trafficking of innate-like lymphocytes, such as γδ T cells and B-1 B cells, has garnered comparatively little attention from the immunological community relative to… (more)

Subjects/Keywords: B-1 B cell; &gamma,&delta; T cells; lymphocyte trafficking; ovine models; skin; Allergy and Immunology; Cell Biology; Immunology and Infectious Disease; Medical Immunology

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APA (6th Edition):

Geherin, S. (2014). Recirculation of Innate Lymphocyte Subsets in the Skin. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1281

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):

Geherin, Skye. “Recirculation of Innate Lymphocyte Subsets in the Skin.” 2014. Thesis, University of Pennsylvania. Accessed August 24, 2019. https://repository.upenn.edu/edissertations/1281.

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

MLA Handbook (7th Edition):

Geherin, Skye. “Recirculation of Innate Lymphocyte Subsets in the Skin.” 2014. Web. 24 Aug 2019.

Vancouver:

Geherin S. Recirculation of Innate Lymphocyte Subsets in the Skin. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2019 Aug 24]. Available from: https://repository.upenn.edu/edissertations/1281.

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

Council of Science Editors:

Geherin S. Recirculation of Innate Lymphocyte Subsets in the Skin. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1281

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

28. Li, Xinrui. Regulation of B cell biology by FCγ receptors.

Degree: PhD, 2009, University of Alabama – Birmingham

B cell development, maturation and proliferation are all strictly regulated processes. Disruption of the regulatory network at any step would lead to immune disorders. The… (more)

Subjects/Keywords: B-Cell Activating Factor  – metabolism<; br>; B-Lymphocytes  – immunology<; br>; Myeloid Cells  – immunology<; br>; Opsonin Proteins  – immunology<; br>; Polymorphism, Single Nucleotide<; br>; Receptors, IgG  – immunology

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APA (6th Edition):

Li, X. (2009). Regulation of B cell biology by FCγ receptors. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,915

Chicago Manual of Style (16th Edition):

Li, Xinrui. “Regulation of B cell biology by FCγ receptors.” 2009. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,915.

MLA Handbook (7th Edition):

Li, Xinrui. “Regulation of B cell biology by FCγ receptors.” 2009. Web. 24 Aug 2019.

Vancouver:

Li X. Regulation of B cell biology by FCγ receptors. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2009. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,915.

Council of Science Editors:

Li X. Regulation of B cell biology by FCγ receptors. [Doctoral Dissertation]. University of Alabama – Birmingham; 2009. Available from: http://contentdm.mhsl.uab.edu/u?/etd,915

29. Martin, Erin. The role of B cell subset in peripheral T cell tolerance induction.

Degree: MS, 2010, Oregon Health Sciences University

Subjects/Keywords: B cells; T cells; Autoimmunity; Peripheral T cell tolerance; B-Lymphocyte Subsets; T-Lymphocytes, Regulatory; Precursor Cells, B-Lymphoid; Autoimmunity

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

APA (6th Edition):

Martin, E. (2010). The role of B cell subset in peripheral T cell tolerance induction. (Thesis). Oregon Health Sciences University. Retrieved from doi:10.6083/M4B27S8C ; http://digitalcommons.ohsu.edu/etd/663

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):

Martin, Erin. “The role of B cell subset in peripheral T cell tolerance induction.” 2010. Thesis, Oregon Health Sciences University. Accessed August 24, 2019. doi:10.6083/M4B27S8C ; http://digitalcommons.ohsu.edu/etd/663.

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

MLA Handbook (7th Edition):

Martin, Erin. “The role of B cell subset in peripheral T cell tolerance induction.” 2010. Web. 24 Aug 2019.

Vancouver:

Martin E. The role of B cell subset in peripheral T cell tolerance induction. [Internet] [Thesis]. Oregon Health Sciences University; 2010. [cited 2019 Aug 24]. Available from: doi:10.6083/M4B27S8C ; http://digitalcommons.ohsu.edu/etd/663.

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

Council of Science Editors:

Martin E. The role of B cell subset in peripheral T cell tolerance induction. [Thesis]. Oregon Health Sciences University; 2010. Available from: doi:10.6083/M4B27S8C ; http://digitalcommons.ohsu.edu/etd/663

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

30. You, Yuying. Cross-talk between marginal zone B cells and marginal zone macrophages.

Degree: PhD, 2010, University of Alabama – Birmingham

The marginal zone (MZ) in the spleen provides a critical defense against bloodborne pathogens. Specialized MZ macrophages (MZM) identified previously based on scavenger receptor (MARCO)… (more)

Subjects/Keywords: Antigens, CD19  – immunology<; br>; Antigens, CD19  – metabolism<; br>; B-Lymphocytes  – cytology<; br>; B-Lymphocytes  – immunology<; br>; Spleen  – cytology<; br>; Spleen  – immunology

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

APA (6th Edition):

You, Y. (2010). Cross-talk between marginal zone B cells and marginal zone macrophages. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,659

Chicago Manual of Style (16th Edition):

You, Yuying. “Cross-talk between marginal zone B cells and marginal zone macrophages.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed August 24, 2019. http://contentdm.mhsl.uab.edu/u?/etd,659.

MLA Handbook (7th Edition):

You, Yuying. “Cross-talk between marginal zone B cells and marginal zone macrophages.” 2010. Web. 24 Aug 2019.

Vancouver:

You Y. Cross-talk between marginal zone B cells and marginal zone macrophages. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2019 Aug 24]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,659.

Council of Science Editors:

You Y. Cross-talk between marginal zone B cells and marginal zone macrophages. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,659

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