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You searched for subject:(B cell development). Showing records 1 – 30 of 33 total matches.

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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 November 11, 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. 11 Nov 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 Nov 11]. 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 Toronto

2. 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 November 11, 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. 11 Nov 2019.

Vancouver:

Ling AK. The Role of BLNK in Avian B-cell Development. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Nov 11]. 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 Utah

3. 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 November 11, 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. 11 Nov 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 Nov 11]. 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


University of Cambridge

4. 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 November 11, 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. 11 Nov 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 Nov 11]. 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 New South Wales

5. Suryani, Santi. Molecular, functional and developmental analysis of B cells at discrete stages of development.

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

 Most of the knowledge of B cell development has been derived from studies in mice. Although many aspects of human B cell development are similar… (more)

Subjects/Keywords: Immunology; B cell; Human; Development; Immunodeficiency

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APA (6th Edition):

Suryani, S. (2010). Molecular, functional and developmental analysis of B cells at discrete stages of development. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50267 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9145/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Suryani, Santi. “Molecular, functional and developmental analysis of B cells at discrete stages of development.” 2010. Doctoral Dissertation, University of New South Wales. Accessed November 11, 2019. http://handle.unsw.edu.au/1959.4/50267 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9145/SOURCE02?view=true.

MLA Handbook (7th Edition):

Suryani, Santi. “Molecular, functional and developmental analysis of B cells at discrete stages of development.” 2010. Web. 11 Nov 2019.

Vancouver:

Suryani S. Molecular, functional and developmental analysis of B cells at discrete stages of development. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Nov 11]. Available from: http://handle.unsw.edu.au/1959.4/50267 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9145/SOURCE02?view=true.

Council of Science Editors:

Suryani S. Molecular, functional and developmental analysis of B cells at discrete stages of development. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50267 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9145/SOURCE02?view=true


Duke University

6. 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 November 11, 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. 11 Nov 2019.

Vancouver:

Holl TM. The Influence of B-cell Tolerance on Humoral Immunity to HIV-1 . [Internet] [Thesis]. Duke University; 2010. [cited 2019 Nov 11]. 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


University of Iowa

7. Hankel, Isaiah Luke. The developmental regulator Gon4-like functions within the transcriptional networks that control B lymphopoiesis and CD4+ T cell responses.

Degree: PhD, Anatomy and Cell Biology, 2011, University of Iowa

B and T lymphocytes are critical to the adaptive immune response against invading microorganisms. B and T cells develop in the bone marrow and… (more)

Subjects/Keywords: B cell; Cell signaling; Development; Lymphocyte; T cell; Transcription factor; Cell Anatomy

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APA (6th Edition):

Hankel, I. L. (2011). The developmental regulator Gon4-like functions within the transcriptional networks that control B lymphopoiesis and CD4+ T cell responses. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/2712

Chicago Manual of Style (16th Edition):

Hankel, Isaiah Luke. “The developmental regulator Gon4-like functions within the transcriptional networks that control B lymphopoiesis and CD4+ T cell responses.” 2011. Doctoral Dissertation, University of Iowa. Accessed November 11, 2019. https://ir.uiowa.edu/etd/2712.

MLA Handbook (7th Edition):

Hankel, Isaiah Luke. “The developmental regulator Gon4-like functions within the transcriptional networks that control B lymphopoiesis and CD4+ T cell responses.” 2011. Web. 11 Nov 2019.

Vancouver:

Hankel IL. The developmental regulator Gon4-like functions within the transcriptional networks that control B lymphopoiesis and CD4+ T cell responses. [Internet] [Doctoral dissertation]. University of Iowa; 2011. [cited 2019 Nov 11]. Available from: https://ir.uiowa.edu/etd/2712.

Council of Science Editors:

Hankel IL. The developmental regulator Gon4-like functions within the transcriptional networks that control B lymphopoiesis and CD4+ T cell responses. [Doctoral Dissertation]. University of Iowa; 2011. Available from: https://ir.uiowa.edu/etd/2712


University of Melbourne

8. Jurado, Sabine. Novel function of the DNA damage response protein ASCIZ as an essential transcription factor.

Degree: 2012, University of Melbourne

 DNA damage repair pathways are important to preserve genome integrity and thereby prevent the onset of cancer. In addition, these pathways are necessary to promote… (more)

Subjects/Keywords: DNA damage; transcription; lung development; B cell development

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APA (6th Edition):

Jurado, S. (2012). Novel function of the DNA damage response protein ASCIZ as an essential transcription factor. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37583

Chicago Manual of Style (16th Edition):

Jurado, Sabine. “Novel function of the DNA damage response protein ASCIZ as an essential transcription factor.” 2012. Doctoral Dissertation, University of Melbourne. Accessed November 11, 2019. http://hdl.handle.net/11343/37583.

MLA Handbook (7th Edition):

Jurado, Sabine. “Novel function of the DNA damage response protein ASCIZ as an essential transcription factor.” 2012. Web. 11 Nov 2019.

Vancouver:

Jurado S. Novel function of the DNA damage response protein ASCIZ as an essential transcription factor. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/11343/37583.

Council of Science Editors:

Jurado S. Novel function of the DNA damage response protein ASCIZ as an essential transcription factor. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37583


Loyola University Chicago

9. Yeramilli, Venkata Arunachalam. B Lymphocyte Development in Galt.

Degree: PhD, Microbiology and Immunology, 2010, Loyola University Chicago

  In rabbits, the primary antibody repertoire is generated in the gut-associated lymphoid tissues (GALT), where bone marrow (BM)-derived B cells undergo a proliferative expansion… (more)

Subjects/Keywords: BAFF; B cell development; B cell maturation; GALT; Homeostasis; Transitional B cells; Immunology and Infectious Disease

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APA (6th Edition):

Yeramilli, V. A. (2010). B Lymphocyte Development in Galt. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/163

Chicago Manual of Style (16th Edition):

Yeramilli, Venkata Arunachalam. “B Lymphocyte Development in Galt.” 2010. Doctoral Dissertation, Loyola University Chicago. Accessed November 11, 2019. https://ecommons.luc.edu/luc_diss/163.

MLA Handbook (7th Edition):

Yeramilli, Venkata Arunachalam. “B Lymphocyte Development in Galt.” 2010. Web. 11 Nov 2019.

Vancouver:

Yeramilli VA. B Lymphocyte Development in Galt. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2010. [cited 2019 Nov 11]. Available from: https://ecommons.luc.edu/luc_diss/163.

Council of Science Editors:

Yeramilli VA. B Lymphocyte Development in Galt. [Doctoral Dissertation]. Loyola University Chicago; 2010. Available from: https://ecommons.luc.edu/luc_diss/163

10. M. Rahmat. FUNCTIONAL DISSECTION OF THE HISTONE DEMETHYLASE JMJD3 IN B CELL LYMPHOPOIESIS.

Degree: 2015, Università degli Studi di Milano

 Histone H3 lysine-27 trimethylation (H3K27me3) is an epigenetic mark that exerts a critical role in heritable gene repression. Levels of H3K27me3 at genomic target sites… (more)

Subjects/Keywords: Jmjd3; B cell development; epigenetics; Settore MED/04 - Patologia Generale

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APA (6th Edition):

Rahmat, M. (2015). FUNCTIONAL DISSECTION OF THE HISTONE DEMETHYLASE JMJD3 IN B CELL LYMPHOPOIESIS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/265225

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):

Rahmat, M.. “FUNCTIONAL DISSECTION OF THE HISTONE DEMETHYLASE JMJD3 IN B CELL LYMPHOPOIESIS.” 2015. Thesis, Università degli Studi di Milano. Accessed November 11, 2019. http://hdl.handle.net/2434/265225.

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

MLA Handbook (7th Edition):

Rahmat, M.. “FUNCTIONAL DISSECTION OF THE HISTONE DEMETHYLASE JMJD3 IN B CELL LYMPHOPOIESIS.” 2015. Web. 11 Nov 2019.

Vancouver:

Rahmat M. FUNCTIONAL DISSECTION OF THE HISTONE DEMETHYLASE JMJD3 IN B CELL LYMPHOPOIESIS. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2434/265225.

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

Council of Science Editors:

Rahmat M. FUNCTIONAL DISSECTION OF THE HISTONE DEMETHYLASE JMJD3 IN B CELL LYMPHOPOIESIS. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/265225

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


Virginia Tech

11. Vieson, Miranda Diane. Selective HDAC6 Inhibition in Systemic Lupus Erythematosus.

Degree: PhD, Veterinary Medicine, 2017, Virginia Tech

 Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease characterized by abnormalities in multiple components of the immune system resulting in progressive damage to multiple… (more)

Subjects/Keywords: Autoimmunity; Histone Deacteylase; Lupus Nephritis; B Cell Development

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APA (6th Edition):

Vieson, M. D. (2017). Selective HDAC6 Inhibition in Systemic Lupus Erythematosus. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/74872

Chicago Manual of Style (16th Edition):

Vieson, Miranda Diane. “Selective HDAC6 Inhibition in Systemic Lupus Erythematosus.” 2017. Doctoral Dissertation, Virginia Tech. Accessed November 11, 2019. http://hdl.handle.net/10919/74872.

MLA Handbook (7th Edition):

Vieson, Miranda Diane. “Selective HDAC6 Inhibition in Systemic Lupus Erythematosus.” 2017. Web. 11 Nov 2019.

Vancouver:

Vieson MD. Selective HDAC6 Inhibition in Systemic Lupus Erythematosus. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/10919/74872.

Council of Science Editors:

Vieson MD. Selective HDAC6 Inhibition in Systemic Lupus Erythematosus. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/74872


University of Melbourne

12. Greig, K. T. Critical roles for the transcription factor c-Myb in early B cell development.

Degree: 2009, University of Melbourne

B cell development is a carefully orchestrated process involving many transcription factors acting in concert with cytokine signals, particularly IL-7. The transcription factor c-Myb has… (more)

Subjects/Keywords: B cell development; c-Myb; hematopoiesis; IL-7; transcription factor

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APA (6th Edition):

Greig, K. T. (2009). Critical roles for the transcription factor c-Myb in early B cell development. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/35130

Chicago Manual of Style (16th Edition):

Greig, K T. “Critical roles for the transcription factor c-Myb in early B cell development.” 2009. Doctoral Dissertation, University of Melbourne. Accessed November 11, 2019. http://hdl.handle.net/11343/35130.

MLA Handbook (7th Edition):

Greig, K T. “Critical roles for the transcription factor c-Myb in early B cell development.” 2009. Web. 11 Nov 2019.

Vancouver:

Greig KT. Critical roles for the transcription factor c-Myb in early B cell development. [Internet] [Doctoral dissertation]. University of Melbourne; 2009. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/11343/35130.

Council of Science Editors:

Greig KT. Critical roles for the transcription factor c-Myb in early B cell development. [Doctoral Dissertation]. University of Melbourne; 2009. Available from: http://hdl.handle.net/11343/35130


Cornell University

13. Kim, Hana. The role of Sel1L-Hrd1 ER Associated Degradation in B cell development and function.

Degree: 2017, Cornell University

 The Endoplasmic Reticulum (ER) serves as the site for protein synthesis, folding, maturation and modification in the cell. In mammalian cells, approximately one-third of the… (more)

Subjects/Keywords: Immunology; B cell development; Colitis; ERAD; IgA; PreBCR; Sel1L-Hrd1

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APA (6th Edition):

Kim, H. (2017). The role of Sel1L-Hrd1 ER Associated Degradation in B cell development and function. (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/56908

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):

Kim, Hana. “The role of Sel1L-Hrd1 ER Associated Degradation in B cell development and function. ” 2017. Thesis, Cornell University. Accessed November 11, 2019. http://hdl.handle.net/1813/56908.

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

MLA Handbook (7th Edition):

Kim, Hana. “The role of Sel1L-Hrd1 ER Associated Degradation in B cell development and function. ” 2017. Web. 11 Nov 2019.

Vancouver:

Kim H. The role of Sel1L-Hrd1 ER Associated Degradation in B cell development and function. [Internet] [Thesis]. Cornell University; 2017. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1813/56908.

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

Council of Science Editors:

Kim H. The role of Sel1L-Hrd1 ER Associated Degradation in B cell development and function. [Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56908

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


Rockefeller University

14. Siegel, Rachael. The Dual Role of OCA-B in B Cell Development and Signaling.

Degree: 2006, Rockefeller University

 OCA-B (Oct coactivator from B cells) is a B-cell specific coactivator of transcription that acts in conjunction with the ubiquitously expressed activator, OCT-1 or the… (more)

Subjects/Keywords: B cell development; OCA-B; B cell receptor signaling; Life Sciences

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APA (6th Edition):

Siegel, R. (2006). The Dual Role of OCA-B in B Cell Development and Signaling. (Masters Thesis). Rockefeller University. Retrieved from https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/62

Chicago Manual of Style (16th Edition):

Siegel, Rachael. “The Dual Role of OCA-B in B Cell Development and Signaling.” 2006. Masters Thesis, Rockefeller University. Accessed November 11, 2019. https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/62.

MLA Handbook (7th Edition):

Siegel, Rachael. “The Dual Role of OCA-B in B Cell Development and Signaling.” 2006. Web. 11 Nov 2019.

Vancouver:

Siegel R. The Dual Role of OCA-B in B Cell Development and Signaling. [Internet] [Masters thesis]. Rockefeller University; 2006. [cited 2019 Nov 11]. Available from: https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/62.

Council of Science Editors:

Siegel R. The Dual Role of OCA-B in B Cell Development and Signaling. [Masters Thesis]. Rockefeller University; 2006. Available from: https://digitalcommons.rockefeller.edu/student_theses_and_dissertations/62


University of Cincinnati

15. Fritz, Jill M. The endoplasmic reticulum chaperone ERdj4 is required for survival, glucose metabolism and B cell development.

Degree: PhD, Medicine: Immunology, 2012, University of Cincinnati

 The ER-localized DnaJ homologue 4 (ERdj4) is a soluble ER chaperone induced by the unfolded protein response (UPR) to assist in the removal of unfolded/misfolded… (more)

Subjects/Keywords: Molecular Biology; ERdj4; UPR; molecular chaperones; endoplasmic reticulum; glucose metabolism; B cell development

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APA (6th Edition):

Fritz, J. M. (2012). The endoplasmic reticulum chaperone ERdj4 is required for survival, glucose metabolism and B cell development. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353950480

Chicago Manual of Style (16th Edition):

Fritz, Jill M. “The endoplasmic reticulum chaperone ERdj4 is required for survival, glucose metabolism and B cell development.” 2012. Doctoral Dissertation, University of Cincinnati. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353950480.

MLA Handbook (7th Edition):

Fritz, Jill M. “The endoplasmic reticulum chaperone ERdj4 is required for survival, glucose metabolism and B cell development.” 2012. Web. 11 Nov 2019.

Vancouver:

Fritz JM. The endoplasmic reticulum chaperone ERdj4 is required for survival, glucose metabolism and B cell development. [Internet] [Doctoral dissertation]. University of Cincinnati; 2012. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353950480.

Council of Science Editors:

Fritz JM. The endoplasmic reticulum chaperone ERdj4 is required for survival, glucose metabolism and B cell development. [Doctoral Dissertation]. University of Cincinnati; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1353950480


University of California – Berkeley

16. Timblin, Greg Alan. Transcriptional control of the recombination activating genes Rag1 and Rag2 in B lymphocytes and non-lymphoid cells.

Degree: Molecular & Cell Biology, 2014, University of California – Berkeley

 Expression of the recombination activating genes Rag1 and Rag2 (Rag) is essential for generation of a diverse B cell antigen receptor repertoire necessary for effective… (more)

Subjects/Keywords: Molecular biology; Immunology; B cell development; c-Myb; Ebf1; Foxo1; Rag genes; transcription

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APA (6th Edition):

Timblin, G. A. (2014). Transcriptional control of the recombination activating genes Rag1 and Rag2 in B lymphocytes and non-lymphoid cells. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/06t8c18t

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):

Timblin, Greg Alan. “Transcriptional control of the recombination activating genes Rag1 and Rag2 in B lymphocytes and non-lymphoid cells.” 2014. Thesis, University of California – Berkeley. Accessed November 11, 2019. http://www.escholarship.org/uc/item/06t8c18t.

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

MLA Handbook (7th Edition):

Timblin, Greg Alan. “Transcriptional control of the recombination activating genes Rag1 and Rag2 in B lymphocytes and non-lymphoid cells.” 2014. Web. 11 Nov 2019.

Vancouver:

Timblin GA. Transcriptional control of the recombination activating genes Rag1 and Rag2 in B lymphocytes and non-lymphoid cells. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2019 Nov 11]. Available from: http://www.escholarship.org/uc/item/06t8c18t.

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

Council of Science Editors:

Timblin GA. Transcriptional control of the recombination activating genes Rag1 and Rag2 in B lymphocytes and non-lymphoid cells. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/06t8c18t

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


Virginia Commonwealth University

17. Gibb, David. ADAM10 is a critical regulator of B cell development, antibody production, and myeloid-derived suppressor cell expansion: Effects of B cell-specific ADAM10 deletion and overexpression in vivo.

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

 Proteolytic processing of transmembrane receptors and ligands can have dramatic effects on cell signaling and subsequent cellular responses. Previous studies demonstrated that a disintegrin and… (more)

Subjects/Keywords: disintegrin and metalloproteinase; Notch; CD23; B cell development; Medicine and Health Sciences

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APA (6th Edition):

Gibb, D. (2010). ADAM10 is a critical regulator of B cell development, antibody production, and myeloid-derived suppressor cell expansion: Effects of B cell-specific ADAM10 deletion and overexpression in vivo. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2269

Chicago Manual of Style (16th Edition):

Gibb, David. “ADAM10 is a critical regulator of B cell development, antibody production, and myeloid-derived suppressor cell expansion: Effects of B cell-specific ADAM10 deletion and overexpression in vivo.” 2010. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 11, 2019. https://scholarscompass.vcu.edu/etd/2269.

MLA Handbook (7th Edition):

Gibb, David. “ADAM10 is a critical regulator of B cell development, antibody production, and myeloid-derived suppressor cell expansion: Effects of B cell-specific ADAM10 deletion and overexpression in vivo.” 2010. Web. 11 Nov 2019.

Vancouver:

Gibb D. ADAM10 is a critical regulator of B cell development, antibody production, and myeloid-derived suppressor cell expansion: Effects of B cell-specific ADAM10 deletion and overexpression in vivo. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2010. [cited 2019 Nov 11]. Available from: https://scholarscompass.vcu.edu/etd/2269.

Council of Science Editors:

Gibb D. ADAM10 is a critical regulator of B cell development, antibody production, and myeloid-derived suppressor cell expansion: Effects of B cell-specific ADAM10 deletion and overexpression in vivo. [Doctoral Dissertation]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/2269


University of Western Ontario

18. Reyes Batista, Carolina. The Role Of Spi-B And Pu.1 Transcription Factors In B Cell Development And In Suppression Of Leukemogenesis.

Degree: 2018, University of Western Ontario

 The E26 transformation-specific transcription factors PU.1 and Spi-B are required for B cell maturation within the bone marrow. PU.1 expression is first detected in hematopoietic… (more)

Subjects/Keywords: B cells; B cell development; transcription factors; PU.1; Spi-B; pre-B cell acute lymphoblastic leukemia; immunology; ChIP-sequencing; RNA-sequencing; Whole-Exome sequencing; mutational signatures; immunoglobulin light chain; V(D)J rearrangement; Cancer Biology; Cell and Developmental Biology; Immunity

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APA (6th Edition):

Reyes Batista, C. (2018). The Role Of Spi-B And Pu.1 Transcription Factors In B Cell Development And In Suppression Of Leukemogenesis. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/5614

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):

Reyes Batista, Carolina. “The Role Of Spi-B And Pu.1 Transcription Factors In B Cell Development And In Suppression Of Leukemogenesis.” 2018. Thesis, University of Western Ontario. Accessed November 11, 2019. https://ir.lib.uwo.ca/etd/5614.

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

MLA Handbook (7th Edition):

Reyes Batista, Carolina. “The Role Of Spi-B And Pu.1 Transcription Factors In B Cell Development And In Suppression Of Leukemogenesis.” 2018. Web. 11 Nov 2019.

Vancouver:

Reyes Batista C. The Role Of Spi-B And Pu.1 Transcription Factors In B Cell Development And In Suppression Of Leukemogenesis. [Internet] [Thesis]. University of Western Ontario; 2018. [cited 2019 Nov 11]. Available from: https://ir.lib.uwo.ca/etd/5614.

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

Council of Science Editors:

Reyes Batista C. The Role Of Spi-B And Pu.1 Transcription Factors In B Cell Development And In Suppression Of Leukemogenesis. [Thesis]. University of Western Ontario; 2018. Available from: https://ir.lib.uwo.ca/etd/5614

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

19. Xiao, Changchun. Regulation of B-cell development and tolerance by different members of the miR-17∼1/492 family microRNAs.

Degree: 2018, Nature Research (part of Springer Nature)

Subjects/Keywords: B-cell; Development and tolerance; miR-17B92; microRNAs; Medicina

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APA (6th Edition):

Xiao, C. (2018). Regulation of B-cell development and tolerance by different members of the miR-17∼1/492 family microRNAs. (Thesis). Nature Research (part of Springer Nature). Retrieved from http://hdl.handle.net/10486/686090

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):

Xiao, Changchun. “Regulation of B-cell development and tolerance by different members of the miR-17∼1/492 family microRNAs.” 2018. Thesis, Nature Research (part of Springer Nature). Accessed November 11, 2019. http://hdl.handle.net/10486/686090.

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

MLA Handbook (7th Edition):

Xiao, Changchun. “Regulation of B-cell development and tolerance by different members of the miR-17∼1/492 family microRNAs.” 2018. Web. 11 Nov 2019.

Vancouver:

Xiao C. Regulation of B-cell development and tolerance by different members of the miR-17∼1/492 family microRNAs. [Internet] [Thesis]. Nature Research (part of Springer Nature); 2018. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/10486/686090.

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

Council of Science Editors:

Xiao C. Regulation of B-cell development and tolerance by different members of the miR-17∼1/492 family microRNAs. [Thesis]. Nature Research (part of Springer Nature); 2018. Available from: http://hdl.handle.net/10486/686090

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

20. A. Chronowska. FUNCTIONAL DISSECTION OF HISTONE LYSINE METHYLATION IN B CELL SPECIFICATION.

Degree: 2011, Università degli Studi di Milano

 Methylation on lysine 4 of histone H3 (H3K4) by the histone methyltransferases (HMTs) of the trithorax group is associated with the activation and maintenance of… (more)

Subjects/Keywords: epigenetics; epigenetic regulation; lymphopoiesis; development; histone; histone methyltransferase; Mll2; H3K4; marginal zone B cell; spleen; Settore BIO/10 - Biochimica

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APA (6th Edition):

Chronowska, A. (2011). FUNCTIONAL DISSECTION OF HISTONE LYSINE METHYLATION IN B CELL SPECIFICATION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/154838

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):

Chronowska, A.. “FUNCTIONAL DISSECTION OF HISTONE LYSINE METHYLATION IN B CELL SPECIFICATION.” 2011. Thesis, Università degli Studi di Milano. Accessed November 11, 2019. http://hdl.handle.net/2434/154838.

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

MLA Handbook (7th Edition):

Chronowska, A.. “FUNCTIONAL DISSECTION OF HISTONE LYSINE METHYLATION IN B CELL SPECIFICATION.” 2011. Web. 11 Nov 2019.

Vancouver:

Chronowska A. FUNCTIONAL DISSECTION OF HISTONE LYSINE METHYLATION IN B CELL SPECIFICATION. [Internet] [Thesis]. Università degli Studi di Milano; 2011. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2434/154838.

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

Council of Science Editors:

Chronowska A. FUNCTIONAL DISSECTION OF HISTONE LYSINE METHYLATION IN B CELL SPECIFICATION. [Thesis]. Università degli Studi di Milano; 2011. Available from: http://hdl.handle.net/2434/154838

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


University of Pennsylvania

21. Weiss, Gretchen E. The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria.

Degree: 2010, University of Pennsylvania

 Immunity to Plasmodium falciparum (Pf), the most deadly agent of malaria, is only acquired after years of repeated infections and appears to wane rapidly without… (more)

Subjects/Keywords: B cell; malaria; pathogen-host interaction; immune modulation; vaccine development; Biology; Immunity; Immunology of Infectious Disease; Medical Immunology; Parasitology

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APA (6th Edition):

Weiss, G. E. (2010). The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/210

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):

Weiss, Gretchen E. “The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria.” 2010. Thesis, University of Pennsylvania. Accessed November 11, 2019. https://repository.upenn.edu/edissertations/210.

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

MLA Handbook (7th Edition):

Weiss, Gretchen E. “The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria.” 2010. Web. 11 Nov 2019.

Vancouver:

Weiss GE. The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2019 Nov 11]. Available from: https://repository.upenn.edu/edissertations/210.

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

Council of Science Editors:

Weiss GE. The Acquisition of Human B Cell Memory in Response to Plasmodium Falciparum Malaria. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/210

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

22. Saintamand, Alexis. Etude du rôle de la région régulatrice en 3' du locus IgH au cours du développement lymphocytaire B normal et pathologique : Study of the role of the regulatory region in 3’ of the IgH locus during normal and pathological B cell development.

Degree: Docteur es, Immunogénétique, 2016, Limoges

Durant l’ontogénie B, le locus des chaines lourdes d’immunoglobulines (IgH) subit trois processus de réarrangements géniques. Lors des phases précoces du développement B, indépendamment de… (more)

Subjects/Keywords: Locus IgH; Ontogénie B; 3'RR; Hypermutation somatique; Recombinaison isotypique; IgH locus; B cell development; 3'RR; Somatic hypermutation; Class switch recombination; 570

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APA (6th Edition):

Saintamand, A. (2016). Etude du rôle de la région régulatrice en 3' du locus IgH au cours du développement lymphocytaire B normal et pathologique : Study of the role of the regulatory region in 3’ of the IgH locus during normal and pathological B cell development. (Doctoral Dissertation). Limoges. Retrieved from http://www.theses.fr/2016LIMO0007

Chicago Manual of Style (16th Edition):

Saintamand, Alexis. “Etude du rôle de la région régulatrice en 3' du locus IgH au cours du développement lymphocytaire B normal et pathologique : Study of the role of the regulatory region in 3’ of the IgH locus during normal and pathological B cell development.” 2016. Doctoral Dissertation, Limoges. Accessed November 11, 2019. http://www.theses.fr/2016LIMO0007.

MLA Handbook (7th Edition):

Saintamand, Alexis. “Etude du rôle de la région régulatrice en 3' du locus IgH au cours du développement lymphocytaire B normal et pathologique : Study of the role of the regulatory region in 3’ of the IgH locus during normal and pathological B cell development.” 2016. Web. 11 Nov 2019.

Vancouver:

Saintamand A. Etude du rôle de la région régulatrice en 3' du locus IgH au cours du développement lymphocytaire B normal et pathologique : Study of the role of the regulatory region in 3’ of the IgH locus during normal and pathological B cell development. [Internet] [Doctoral dissertation]. Limoges; 2016. [cited 2019 Nov 11]. Available from: http://www.theses.fr/2016LIMO0007.

Council of Science Editors:

Saintamand A. Etude du rôle de la région régulatrice en 3' du locus IgH au cours du développement lymphocytaire B normal et pathologique : Study of the role of the regulatory region in 3’ of the IgH locus during normal and pathological B cell development. [Doctoral Dissertation]. Limoges; 2016. Available from: http://www.theses.fr/2016LIMO0007


Loma Linda University

23. Benitez, Abigail. CD21 and CD24 Co-expression: A Translational Model between Mouse and Human.

Degree: PhD, Basic Sciences, 2014, Loma Linda University

  Systemic Lupus Erythematosus and Rheumatoid Arthritis are B cell-mediated autoimmune diseases that afflict millions of people worldwide. B cell-targeted therapies for these diseases result… (more)

Subjects/Keywords: Genetics and Genomics; Life Sciences; Medicine and Health Sciences; Microbiology; Molecular Genetics; Antigens - Differentiation; Antigens - CD24; Receptors - Complement 3d; B-Lymphocyte Subset; B-Cell Activating Factor; Lymphoid Progenitor Cells; Hematopoietic Stem Cells; Immunoglobulin Light Chains; Common Variable Immunodeficiency; Species Specificity; Systemic Lupus Erythematosus; Rheumatoid Arthritis; B cell-mediated autoimmune diseases; Mouse model; Human B Cell development

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APA (6th Edition):

Benitez, A. (2014). CD21 and CD24 Co-expression: A Translational Model between Mouse and Human. (Doctoral Dissertation). Loma Linda University. Retrieved from https://scholarsrepository.llu.edu/etd/198

Chicago Manual of Style (16th Edition):

Benitez, Abigail. “CD21 and CD24 Co-expression: A Translational Model between Mouse and Human.” 2014. Doctoral Dissertation, Loma Linda University. Accessed November 11, 2019. https://scholarsrepository.llu.edu/etd/198.

MLA Handbook (7th Edition):

Benitez, Abigail. “CD21 and CD24 Co-expression: A Translational Model between Mouse and Human.” 2014. Web. 11 Nov 2019.

Vancouver:

Benitez A. CD21 and CD24 Co-expression: A Translational Model between Mouse and Human. [Internet] [Doctoral dissertation]. Loma Linda University; 2014. [cited 2019 Nov 11]. Available from: https://scholarsrepository.llu.edu/etd/198.

Council of Science Editors:

Benitez A. CD21 and CD24 Co-expression: A Translational Model between Mouse and Human. [Doctoral Dissertation]. Loma Linda University; 2014. Available from: https://scholarsrepository.llu.edu/etd/198


Vanderbilt University

24. Llanes, Joan Manuel. Signaling regulation of transitional immature to mature B cell development.

Degree: MS, Microbiology and Immunology, 2006, Vanderbilt University

 The immature B cell compartment in the spleen comprises of two subsets termed Transitional Type 1 (T1) and Transitional Type 2 (T2). Our laboratory has… (more)

Subjects/Keywords: B cells Differentiation Molecular aspects; B cell development; B cell receptor signaling; Cellular control mechanisms

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APA (6th Edition):

Llanes, J. M. (2006). Signaling regulation of transitional immature to mature B cell development. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07172006-115717/ ;

Chicago Manual of Style (16th Edition):

Llanes, Joan Manuel. “Signaling regulation of transitional immature to mature B cell development.” 2006. Masters Thesis, Vanderbilt University. Accessed November 11, 2019. http://etd.library.vanderbilt.edu/available/etd-07172006-115717/ ;.

MLA Handbook (7th Edition):

Llanes, Joan Manuel. “Signaling regulation of transitional immature to mature B cell development.” 2006. Web. 11 Nov 2019.

Vancouver:

Llanes JM. Signaling regulation of transitional immature to mature B cell development. [Internet] [Masters thesis]. Vanderbilt University; 2006. [cited 2019 Nov 11]. Available from: http://etd.library.vanderbilt.edu/available/etd-07172006-115717/ ;.

Council of Science Editors:

Llanes JM. Signaling regulation of transitional immature to mature B cell development. [Masters Thesis]. Vanderbilt University; 2006. Available from: http://etd.library.vanderbilt.edu/available/etd-07172006-115717/ ;


The Ohio State University

25. Chen, Hui-Chen. Role for cyclic adenosine monophosphate (cAMP) response element binding proteins in B lymphocyte development and functional maturation.

Degree: PhD, Medical Microbiology and Immunology, 2003, The Ohio State University

 Cyclic adenosine 5’ monophosphate (cAMP) response element binding protein-1 (CREB-1) belongs to the CREB/ATF leucine zipper family of transcription factors. CREB-1 is expressed in pro-B,… (more)

Subjects/Keywords: Health Sciences, Immunology; CREB-1; B lymphocytes; B1 B cells; B2 B cells; Immune response; B cell development

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APA (6th Edition):

Chen, H. (2003). Role for cyclic adenosine monophosphate (cAMP) response element binding proteins in B lymphocyte development and functional maturation. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1061213266

Chicago Manual of Style (16th Edition):

Chen, Hui-Chen. “Role for cyclic adenosine monophosphate (cAMP) response element binding proteins in B lymphocyte development and functional maturation.” 2003. Doctoral Dissertation, The Ohio State University. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1061213266.

MLA Handbook (7th Edition):

Chen, Hui-Chen. “Role for cyclic adenosine monophosphate (cAMP) response element binding proteins in B lymphocyte development and functional maturation.” 2003. Web. 11 Nov 2019.

Vancouver:

Chen H. Role for cyclic adenosine monophosphate (cAMP) response element binding proteins in B lymphocyte development and functional maturation. [Internet] [Doctoral dissertation]. The Ohio State University; 2003. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1061213266.

Council of Science Editors:

Chen H. Role for cyclic adenosine monophosphate (cAMP) response element binding proteins in B lymphocyte development and functional maturation. [Doctoral Dissertation]. The Ohio State University; 2003. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1061213266


Cornell University

26. Daley, Lisa. The significance of heavy-chain antibodies to camelid immunity .

Degree: 2007, Cornell University

 Camelids produce IgG isotypes that do not conform to the rules governing conventional antibody structures. Typically, immunoglobulins combine homodimeric heavy and light chains to produce… (more)

Subjects/Keywords: Heavy-chain antibodies; camelid; anti-nematode IgGs; anti-viral IgGs; B cell development; B cell distribution; colostrum; IgG-specific monoclonal antibodies

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APA (6th Edition):

Daley, L. (2007). The significance of heavy-chain antibodies to camelid immunity . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/7552

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):

Daley, Lisa. “The significance of heavy-chain antibodies to camelid immunity .” 2007. Thesis, Cornell University. Accessed November 11, 2019. http://hdl.handle.net/1813/7552.

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

MLA Handbook (7th Edition):

Daley, Lisa. “The significance of heavy-chain antibodies to camelid immunity .” 2007. Web. 11 Nov 2019.

Vancouver:

Daley L. The significance of heavy-chain antibodies to camelid immunity . [Internet] [Thesis]. Cornell University; 2007. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1813/7552.

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

Council of Science Editors:

Daley L. The significance of heavy-chain antibodies to camelid immunity . [Thesis]. Cornell University; 2007. Available from: http://hdl.handle.net/1813/7552

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


Loma Linda University

27. Milford, Terry-Ann. Comparative Studies of TSLP and IL-7 in Normal Early Human Neonatal and Adult B Cell Development.

Degree: PhD, Basic Sciences, 2016, Loma Linda University

  Defining the role of cytokines in promoting human B cell development is important for understanding B cell leukemia and for developing strategies to restore… (more)

Subjects/Keywords: Medical Genetics; Medical Microbiology; Medicine and Health Sciences; Microbiology; Molecular Genetics; Cytokines  – Genetics; Cytokines  – Physiology; B Lymphocytes; Precursor Cell Lymphoblastic Leukemia-Lymphoma;

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APA (6th Edition):

Milford, T. (2016). Comparative Studies of TSLP and IL-7 in Normal Early Human Neonatal and Adult B Cell Development. (Doctoral Dissertation). Loma Linda University. Retrieved from https://scholarsrepository.llu.edu/etd/402

Chicago Manual of Style (16th Edition):

Milford, Terry-Ann. “Comparative Studies of TSLP and IL-7 in Normal Early Human Neonatal and Adult B Cell Development.” 2016. Doctoral Dissertation, Loma Linda University. Accessed November 11, 2019. https://scholarsrepository.llu.edu/etd/402.

MLA Handbook (7th Edition):

Milford, Terry-Ann. “Comparative Studies of TSLP and IL-7 in Normal Early Human Neonatal and Adult B Cell Development.” 2016. Web. 11 Nov 2019.

Vancouver:

Milford T. Comparative Studies of TSLP and IL-7 in Normal Early Human Neonatal and Adult B Cell Development. [Internet] [Doctoral dissertation]. Loma Linda University; 2016. [cited 2019 Nov 11]. Available from: https://scholarsrepository.llu.edu/etd/402.

Council of Science Editors:

Milford T. Comparative Studies of TSLP and IL-7 in Normal Early Human Neonatal and Adult B Cell Development. [Doctoral Dissertation]. Loma Linda University; 2016. Available from: https://scholarsrepository.llu.edu/etd/402


University of Oulu

28. Syrjänen, R. (Riikka). TIM family molecules in hematopoiesis.

Degree: 2014, University of Oulu

Abstract Hematopoietic cells, i.e., erythrocytes, platelets and white blood cells, differentiate from hematopoietic stem cells in a process that is similar in vertebrates. Hematopoiesis is… (more)

Subjects/Keywords: B cell development; fetal liver; gene expression; hematopoiesis; myeloid progenitor cells; para-aortic region; transmembrane immunoglobulin and mucin domain containing molecule; B-solujen kehitys; alkion maksa; geeniekspressio; hematopoieesi; myeloidiset esisolut; para-aortaalinen alue; transmembrane immunoglobulin and mucin domain containing -molekyyli

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APA (6th Edition):

Syrjänen, R. (. (2014). TIM family molecules in hematopoiesis. (Doctoral Dissertation). University of Oulu. Retrieved from http://urn.fi/urn:isbn:9789526204246

Chicago Manual of Style (16th Edition):

Syrjänen, R (Riikka). “TIM family molecules in hematopoiesis.” 2014. Doctoral Dissertation, University of Oulu. Accessed November 11, 2019. http://urn.fi/urn:isbn:9789526204246.

MLA Handbook (7th Edition):

Syrjänen, R (Riikka). “TIM family molecules in hematopoiesis.” 2014. Web. 11 Nov 2019.

Vancouver:

Syrjänen R(. TIM family molecules in hematopoiesis. [Internet] [Doctoral dissertation]. University of Oulu; 2014. [cited 2019 Nov 11]. Available from: http://urn.fi/urn:isbn:9789526204246.

Council of Science Editors:

Syrjänen R(. TIM family molecules in hematopoiesis. [Doctoral Dissertation]. University of Oulu; 2014. Available from: http://urn.fi/urn:isbn:9789526204246

29. Barr, Jennifer Yamaoka. The Justy mutation disrupts the regulation of gene expression and cell cycle progression during B lymphopoiesis.

Degree: PhD, Anatomy and Cell Biology, 2015, University of Iowa

B lymphopoiesis requires a network of transcription factors that orchestrate changes in gene expression amidst immunoglobulin gene rearrangement and periods of cell proliferation. Although… (more)

Subjects/Keywords: publicabstract; B cell development; Cell cycle; Cyclin D3; Gene expression; Gon4-like; proliferation; Cell Anatomy; Cell Biology

cell development is intact in Justy B cell progenitors, yet these cells fail to repress genes… …that promote the development of alternative lineages. In addition, Justy B cell progenitors… …rescued pro-B cell development from Justy progenitors, an effect that was not observed upon… …regulation of B cell development. Gon4-like has not been well studied in mammals and its role in B… …8 A transcription factor network regulates B cell development… 

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

APA (6th Edition):

Barr, J. Y. (2015). The Justy mutation disrupts the regulation of gene expression and cell cycle progression during B lymphopoiesis. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1542

Chicago Manual of Style (16th Edition):

Barr, Jennifer Yamaoka. “The Justy mutation disrupts the regulation of gene expression and cell cycle progression during B lymphopoiesis.” 2015. Doctoral Dissertation, University of Iowa. Accessed November 11, 2019. https://ir.uiowa.edu/etd/1542.

MLA Handbook (7th Edition):

Barr, Jennifer Yamaoka. “The Justy mutation disrupts the regulation of gene expression and cell cycle progression during B lymphopoiesis.” 2015. Web. 11 Nov 2019.

Vancouver:

Barr JY. The Justy mutation disrupts the regulation of gene expression and cell cycle progression during B lymphopoiesis. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2019 Nov 11]. Available from: https://ir.uiowa.edu/etd/1542.

Council of Science Editors:

Barr JY. The Justy mutation disrupts the regulation of gene expression and cell cycle progression during B lymphopoiesis. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/1542

30. Chow, Kwan Ting. Transcriptional Regulation of the V(D)J Recombinase (Rag).

Degree: Molecular & Cell Biology, 2013, University of California – Berkeley

 Tight regulation of RAG activity is required for proper development of the adaptive immune system as well as prevention of genomic instability. Foxo1 and GFI… (more)

Subjects/Keywords: Molecular biology; Immunology; B cell development; Foxo1; GFI1; MK5; Rag; V(D)J Recombination

…4 B cell development… …5 Rag expression and regulation during B cell development… …16 Figure 1.6. Rag expression during B cell development… …frequently leads to development of pro-B cell lymphoma initiated by IgH-Myc translocation (Zhu… …5 Rag expression and regulation during B cell development RAG activity is tightly linked… 

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

APA (6th Edition):

Chow, K. T. (2013). Transcriptional Regulation of the V(D)J Recombinase (Rag). (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/39d5k662

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):

Chow, Kwan Ting. “Transcriptional Regulation of the V(D)J Recombinase (Rag).” 2013. Thesis, University of California – Berkeley. Accessed November 11, 2019. http://www.escholarship.org/uc/item/39d5k662.

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

MLA Handbook (7th Edition):

Chow, Kwan Ting. “Transcriptional Regulation of the V(D)J Recombinase (Rag).” 2013. Web. 11 Nov 2019.

Vancouver:

Chow KT. Transcriptional Regulation of the V(D)J Recombinase (Rag). [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Nov 11]. Available from: http://www.escholarship.org/uc/item/39d5k662.

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

Council of Science Editors:

Chow KT. Transcriptional Regulation of the V(D)J Recombinase (Rag). [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/39d5k662

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

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