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You searched for subject:(Fc receptor). Showing records 1 – 30 of 47 total matches.

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Boston University

1. Piche-Nicholas, Nicole Melissa. Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor.

Degree: 2014, Boston University

 A large body of data exists demonstrating the key role of FcRn in extending the half-life of therapeutic antibodies by rescuing them from lysosomal degradation.… (more)

Subjects/Keywords: Pharmacology; FcRn; IgG; Neonatal Fc receptor

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

APA (6th Edition):

Piche-Nicholas, N. M. (2014). Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/14377

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):

Piche-Nicholas, Nicole Melissa. “Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor.” 2014. Thesis, Boston University. Accessed July 16, 2019. http://hdl.handle.net/2144/14377.

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

MLA Handbook (7th Edition):

Piche-Nicholas, Nicole Melissa. “Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor.” 2014. Web. 16 Jul 2019.

Vancouver:

Piche-Nicholas NM. Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor. [Internet] [Thesis]. Boston University; 2014. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/2144/14377.

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

Council of Science Editors:

Piche-Nicholas NM. Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor. [Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14377

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

2. Paschoalato, Adriana Balbina Paoliello. Avaliação do metabolismo oxidativo de polimordonucleares mediado por receptores para IgG e para o complemento em pacientes com artrite reumatóide em diferentes estágios da doença.

Degree: PhD, Produtos Naturais e Sintéticos, 2007, University of São Paulo

 A Artrite reumatóide (AR) é uma doença inflamatória crônica e sistêmica, de etiologia desconhecida, que pode dificultar ou impossibilitar as funções habituais das articulações devido… (more)

Subjects/Keywords: artrite reumatóide; complement system; complement receptor; Fc-gamma receptor; metabolismo oxidativo; neutrófilos; neutrophils; oxidative metabolism; receptor CR.; receptor Fc -gamma; rheumatoid arthritis; sistema complemento

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APA (6th Edition):

Paschoalato, A. B. P. (2007). Avaliação do metabolismo oxidativo de polimordonucleares mediado por receptores para IgG e para o complemento em pacientes com artrite reumatóide em diferentes estágios da doença. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60138/tde-29032012-104850/ ;

Chicago Manual of Style (16th Edition):

Paschoalato, Adriana Balbina Paoliello. “Avaliação do metabolismo oxidativo de polimordonucleares mediado por receptores para IgG e para o complemento em pacientes com artrite reumatóide em diferentes estágios da doença.” 2007. Doctoral Dissertation, University of São Paulo. Accessed July 16, 2019. http://www.teses.usp.br/teses/disponiveis/60/60138/tde-29032012-104850/ ;.

MLA Handbook (7th Edition):

Paschoalato, Adriana Balbina Paoliello. “Avaliação do metabolismo oxidativo de polimordonucleares mediado por receptores para IgG e para o complemento em pacientes com artrite reumatóide em diferentes estágios da doença.” 2007. Web. 16 Jul 2019.

Vancouver:

Paschoalato ABP. Avaliação do metabolismo oxidativo de polimordonucleares mediado por receptores para IgG e para o complemento em pacientes com artrite reumatóide em diferentes estágios da doença. [Internet] [Doctoral dissertation]. University of São Paulo; 2007. [cited 2019 Jul 16]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60138/tde-29032012-104850/ ;.

Council of Science Editors:

Paschoalato ABP. Avaliação do metabolismo oxidativo de polimordonucleares mediado por receptores para IgG e para o complemento em pacientes com artrite reumatóide em diferentes estágios da doença. [Doctoral Dissertation]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/60/60138/tde-29032012-104850/ ;


Universiteit Utrecht

3. Karambela, A.E. The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers.

Degree: 2010, Universiteit Utrecht

 The vertebrate immune system has evolved to become particularly good at protecting an organism from extrinsic pathogens such as bacterial and fungal infections. Today the… (more)

Subjects/Keywords: pharmacogenetics; fc receptor; monoclonal antibody; mAB; cancer; polymorphism

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APA (6th Edition):

Karambela, A. E. (2010). The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/188148

Chicago Manual of Style (16th Edition):

Karambela, A E. “The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers.” 2010. Masters Thesis, Universiteit Utrecht. Accessed July 16, 2019. http://dspace.library.uu.nl:8080/handle/1874/188148.

MLA Handbook (7th Edition):

Karambela, A E. “The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers.” 2010. Web. 16 Jul 2019.

Vancouver:

Karambela AE. The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers. [Internet] [Masters thesis]. Universiteit Utrecht; 2010. [cited 2019 Jul 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/188148.

Council of Science Editors:

Karambela AE. The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers. [Masters Thesis]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/188148


Georgia State University

4. Nguyen, Doan C. Immunoglobulin Gamma Subclasses and Corresponding Fc Receptors in Rhesus Macaques: Genetic Characterization and Engineering of Recombinant Molecules.

Degree: PhD, Biology, 2012, Georgia State University

  Rhesus macaques represent a valuable model in biomedical research and in development of vaccines and therapeutics. Due to the lack of reagents, the general… (more)

Subjects/Keywords: Rhesus macaque; IgG; Fc receptor; Polymorphism; Recombinant; Estrogen; Influenza

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APA (6th Edition):

Nguyen, D. C. (2012). Immunoglobulin Gamma Subclasses and Corresponding Fc Receptors in Rhesus Macaques: Genetic Characterization and Engineering of Recombinant Molecules. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/111

Chicago Manual of Style (16th Edition):

Nguyen, Doan C. “Immunoglobulin Gamma Subclasses and Corresponding Fc Receptors in Rhesus Macaques: Genetic Characterization and Engineering of Recombinant Molecules.” 2012. Doctoral Dissertation, Georgia State University. Accessed July 16, 2019. https://scholarworks.gsu.edu/biology_diss/111.

MLA Handbook (7th Edition):

Nguyen, Doan C. “Immunoglobulin Gamma Subclasses and Corresponding Fc Receptors in Rhesus Macaques: Genetic Characterization and Engineering of Recombinant Molecules.” 2012. Web. 16 Jul 2019.

Vancouver:

Nguyen DC. Immunoglobulin Gamma Subclasses and Corresponding Fc Receptors in Rhesus Macaques: Genetic Characterization and Engineering of Recombinant Molecules. [Internet] [Doctoral dissertation]. Georgia State University; 2012. [cited 2019 Jul 16]. Available from: https://scholarworks.gsu.edu/biology_diss/111.

Council of Science Editors:

Nguyen DC. Immunoglobulin Gamma Subclasses and Corresponding Fc Receptors in Rhesus Macaques: Genetic Characterization and Engineering of Recombinant Molecules. [Doctoral Dissertation]. Georgia State University; 2012. Available from: https://scholarworks.gsu.edu/biology_diss/111


Texas A&M University

5. Xiang, Wang. Inhibiting Serum Amyloid P - FcɣR1 Interactions on Human Macrophages Decreases Numbers of Intracellular Mycobacteria.

Degree: MS, Biology, 2018, Texas A&M University

 Macrophages are a heterogeneous population of cells and, include classically activated macrophages (M1) and alternatively activated macrophages (M2). Macrophages can change from M1 to M2… (more)

Subjects/Keywords: M1 macrophage; M2 macrophage; M. smegmatis; M. tuberculosis; SAP; Fc receptor

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APA (6th Edition):

Xiang, W. (2018). Inhibiting Serum Amyloid P - FcɣR1 Interactions on Human Macrophages Decreases Numbers of Intracellular Mycobacteria. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173954

Chicago Manual of Style (16th Edition):

Xiang, Wang. “Inhibiting Serum Amyloid P - FcɣR1 Interactions on Human Macrophages Decreases Numbers of Intracellular Mycobacteria.” 2018. Masters Thesis, Texas A&M University. Accessed July 16, 2019. http://hdl.handle.net/1969.1/173954.

MLA Handbook (7th Edition):

Xiang, Wang. “Inhibiting Serum Amyloid P - FcɣR1 Interactions on Human Macrophages Decreases Numbers of Intracellular Mycobacteria.” 2018. Web. 16 Jul 2019.

Vancouver:

Xiang W. Inhibiting Serum Amyloid P - FcɣR1 Interactions on Human Macrophages Decreases Numbers of Intracellular Mycobacteria. [Internet] [Masters thesis]. Texas A&M University; 2018. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1969.1/173954.

Council of Science Editors:

Xiang W. Inhibiting Serum Amyloid P - FcɣR1 Interactions on Human Macrophages Decreases Numbers of Intracellular Mycobacteria. [Masters Thesis]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173954


Boston University

6. Moody, Krishna Laroche. Attenuation of B cell receptor-toll like receptor responses by Fc gamma receptor IIB.

Degree: PhD, Microbiology, 2016, Boston University

 The pathogenesis of lupus and other autoimmune diseases driven by antibody-antigen complexes involves interactions between genetic and environmental factors. The genetic factors can be separated… (more)

Subjects/Keywords: Immunology; Fc; Autoimmunity; Immune complex; Lupus; Somatic hypermutation; Toll-like receptor

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APA (6th Edition):

Moody, K. L. (2016). Attenuation of B cell receptor-toll like receptor responses by Fc gamma receptor IIB. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16725

Chicago Manual of Style (16th Edition):

Moody, Krishna Laroche. “Attenuation of B cell receptor-toll like receptor responses by Fc gamma receptor IIB.” 2016. Doctoral Dissertation, Boston University. Accessed July 16, 2019. http://hdl.handle.net/2144/16725.

MLA Handbook (7th Edition):

Moody, Krishna Laroche. “Attenuation of B cell receptor-toll like receptor responses by Fc gamma receptor IIB.” 2016. Web. 16 Jul 2019.

Vancouver:

Moody KL. Attenuation of B cell receptor-toll like receptor responses by Fc gamma receptor IIB. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/2144/16725.

Council of Science Editors:

Moody KL. Attenuation of B cell receptor-toll like receptor responses by Fc gamma receptor IIB. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/16725


University of Manitoba

7. Redhu, Naresh Singh. Molecular regulation and effector functions of the high affinity IgE receptor (FcεRI) in human airway smooth muscle cells.

Degree: Immunology, 2012, University of Manitoba

 The prevalence and economic burden of chronic airway disorders such as asthma is on the rise annually. Allergic asthma is characterized by chronic airway inflammation,… (more)

Subjects/Keywords: asthma; airway smooth muscle; IgE; Fc receptor; TSLP; inflammation

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APA (6th Edition):

Redhu, N. S. (2012). Molecular regulation and effector functions of the high affinity IgE receptor (FcεRI) in human airway smooth muscle cells. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/5305

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):

Redhu, Naresh Singh. “Molecular regulation and effector functions of the high affinity IgE receptor (FcεRI) in human airway smooth muscle cells.” 2012. Thesis, University of Manitoba. Accessed July 16, 2019. http://hdl.handle.net/1993/5305.

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

MLA Handbook (7th Edition):

Redhu, Naresh Singh. “Molecular regulation and effector functions of the high affinity IgE receptor (FcεRI) in human airway smooth muscle cells.” 2012. Web. 16 Jul 2019.

Vancouver:

Redhu NS. Molecular regulation and effector functions of the high affinity IgE receptor (FcεRI) in human airway smooth muscle cells. [Internet] [Thesis]. University of Manitoba; 2012. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1993/5305.

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

Council of Science Editors:

Redhu NS. Molecular regulation and effector functions of the high affinity IgE receptor (FcεRI) in human airway smooth muscle cells. [Thesis]. University of Manitoba; 2012. Available from: http://hdl.handle.net/1993/5305

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


Boston University

8. Gubbala, Supreetha. Characterization of Fc receptor family proteins in vaginal and endocervical epithelia.

Degree: MS, Medical Sciences, 2014, Boston University

 In the age of highly active antiretroviral therapy (HAART), patients infected with Human Immunodeficiency Virus Type 1 (HIV-1) are now living significantly healthier and longer… (more)

Subjects/Keywords: Microbiology; HIV; Microbicide; Plantibodies; Monoclonal antibodies; Mucosal immunology; Neonatal Fc receptor

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APA (6th Edition):

Gubbala, S. (2014). Characterization of Fc receptor family proteins in vaginal and endocervical epithelia. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/14659

Chicago Manual of Style (16th Edition):

Gubbala, Supreetha. “Characterization of Fc receptor family proteins in vaginal and endocervical epithelia.” 2014. Masters Thesis, Boston University. Accessed July 16, 2019. http://hdl.handle.net/2144/14659.

MLA Handbook (7th Edition):

Gubbala, Supreetha. “Characterization of Fc receptor family proteins in vaginal and endocervical epithelia.” 2014. Web. 16 Jul 2019.

Vancouver:

Gubbala S. Characterization of Fc receptor family proteins in vaginal and endocervical epithelia. [Internet] [Masters thesis]. Boston University; 2014. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/2144/14659.

Council of Science Editors:

Gubbala S. Characterization of Fc receptor family proteins in vaginal and endocervical epithelia. [Masters Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14659


Georgia State University

9. Masseoud, Feda N. Estrogen-Induced Modulation of Innate and Adaptive Immune Function.

Degree: PhD, Biology, 2009, Georgia State University

 Host defense against infection and disease relies on the reciprocal communication between the immune and neuroendocrine systems where sex hormones exert negative and positive feedback… (more)

Subjects/Keywords: Fc gamma receptor; sex hormones; vaccine response; immunomodulator; autoimmunity; TLR2; antibody responses; Estradiol; Biology

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APA (6th Edition):

Masseoud, F. N. (2009). Estrogen-Induced Modulation of Innate and Adaptive Immune Function. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/62

Chicago Manual of Style (16th Edition):

Masseoud, Feda N. “Estrogen-Induced Modulation of Innate and Adaptive Immune Function.” 2009. Doctoral Dissertation, Georgia State University. Accessed July 16, 2019. https://scholarworks.gsu.edu/biology_diss/62.

MLA Handbook (7th Edition):

Masseoud, Feda N. “Estrogen-Induced Modulation of Innate and Adaptive Immune Function.” 2009. Web. 16 Jul 2019.

Vancouver:

Masseoud FN. Estrogen-Induced Modulation of Innate and Adaptive Immune Function. [Internet] [Doctoral dissertation]. Georgia State University; 2009. [cited 2019 Jul 16]. Available from: https://scholarworks.gsu.edu/biology_diss/62.

Council of Science Editors:

Masseoud FN. Estrogen-Induced Modulation of Innate and Adaptive Immune Function. [Doctoral Dissertation]. Georgia State University; 2009. Available from: https://scholarworks.gsu.edu/biology_diss/62


Loyola University Chicago

10. Karavitis, John. Ethanol Impairs Mechanisms of Macrophage Phagocytosis and Cytokine Production.

Degree: PhD, Cell Biology, Neurobiology and Anatomy, 2010, Loyola University Chicago

  Extensive evidence indicates that alcohol (ethanol) consumption affects human health by altering normal physiological functions of the immune system. This study investigated the effect… (more)

Subjects/Keywords: actin; adhesion; Alcohol; cytoskeleton; Fc gamma Receptor; phagosomal adhesion; Immunology and Infectious Disease

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APA (6th Edition):

Karavitis, J. (2010). Ethanol Impairs Mechanisms of Macrophage Phagocytosis and Cytokine Production. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/165

Chicago Manual of Style (16th Edition):

Karavitis, John. “Ethanol Impairs Mechanisms of Macrophage Phagocytosis and Cytokine Production.” 2010. Doctoral Dissertation, Loyola University Chicago. Accessed July 16, 2019. https://ecommons.luc.edu/luc_diss/165.

MLA Handbook (7th Edition):

Karavitis, John. “Ethanol Impairs Mechanisms of Macrophage Phagocytosis and Cytokine Production.” 2010. Web. 16 Jul 2019.

Vancouver:

Karavitis J. Ethanol Impairs Mechanisms of Macrophage Phagocytosis and Cytokine Production. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2010. [cited 2019 Jul 16]. Available from: https://ecommons.luc.edu/luc_diss/165.

Council of Science Editors:

Karavitis J. Ethanol Impairs Mechanisms of Macrophage Phagocytosis and Cytokine Production. [Doctoral Dissertation]. Loyola University Chicago; 2010. Available from: https://ecommons.luc.edu/luc_diss/165


University of Toronto

11. Tong, Tik Nga. Optimal Conditions for the Monocyte Monolayer Assay and Applications of the Assay.

Degree: 2016, University of Toronto

Immune-mediated hemolysis, whether due to transfusion of incompatible red blood cells (RBCs) in hemolytic transfusion reactions or passive transfer of anti-RBC antibodies through intravenous immunoglobulin… (more)

Subjects/Keywords: Fc gamma receptor; Hemolysis; Monocyte monolayer assay; Red blood cells; Storage; Transfusion; 0564

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APA (6th Edition):

Tong, T. N. (2016). Optimal Conditions for the Monocyte Monolayer Assay and Applications of the Assay. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76076

Chicago Manual of Style (16th Edition):

Tong, Tik Nga. “Optimal Conditions for the Monocyte Monolayer Assay and Applications of the Assay.” 2016. Masters Thesis, University of Toronto. Accessed July 16, 2019. http://hdl.handle.net/1807/76076.

MLA Handbook (7th Edition):

Tong, Tik Nga. “Optimal Conditions for the Monocyte Monolayer Assay and Applications of the Assay.” 2016. Web. 16 Jul 2019.

Vancouver:

Tong TN. Optimal Conditions for the Monocyte Monolayer Assay and Applications of the Assay. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1807/76076.

Council of Science Editors:

Tong TN. Optimal Conditions for the Monocyte Monolayer Assay and Applications of the Assay. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76076

12. WU XIAOWEI. Investigation of Interleukin 1B synthesis and secretion by dendritic cells: Interplay between toll-like receptor and FCG receptor.

Degree: 2007, National University of Singapore

Subjects/Keywords: Interleukin 1B; dendritic cells; Fc gamma receptor; P2X7 receptor

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APA (6th Edition):

XIAOWEI, W. (2007). Investigation of Interleukin 1B synthesis and secretion by dendritic cells: Interplay between toll-like receptor and FCG receptor. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/17539

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):

XIAOWEI, WU. “Investigation of Interleukin 1B synthesis and secretion by dendritic cells: Interplay between toll-like receptor and FCG receptor.” 2007. Thesis, National University of Singapore. Accessed July 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/17539.

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

MLA Handbook (7th Edition):

XIAOWEI, WU. “Investigation of Interleukin 1B synthesis and secretion by dendritic cells: Interplay between toll-like receptor and FCG receptor.” 2007. Web. 16 Jul 2019.

Vancouver:

XIAOWEI W. Investigation of Interleukin 1B synthesis and secretion by dendritic cells: Interplay between toll-like receptor and FCG receptor. [Internet] [Thesis]. National University of Singapore; 2007. [cited 2019 Jul 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/17539.

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

Council of Science Editors:

XIAOWEI W. Investigation of Interleukin 1B synthesis and secretion by dendritic cells: Interplay between toll-like receptor and FCG receptor. [Thesis]. National University of Singapore; 2007. Available from: http://scholarbank.nus.edu.sg/handle/10635/17539

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

13. Brachet, Guillaume. Déterminants moléculaires de la pharmacocinétique des anticorps thérapeutiques : Molecular determinants of monoclonal antibody pharmacokinetics.

Degree: Docteur es, Immunologie, 2017, Université François-Rabelais de Tours

La pharmacocinétique (PK) des anticorps monoclonaux (mAbs) est sujette à d’importantes variations interindividuelles. Le récepteur néonatal au Fc des IgG (FcRn) et le statut immun… (more)

Subjects/Keywords: Pharmacocinétique; Anticorps monoclonaux thérapeutiques; Anticorps armés; Récepteur néonatal au Fc des IgG; Agrégats; Complexes immuns; Pharmacokinetics; Therapeutic monoclonal antibodies; Antibody-drug-conjugates; Neonatal Fc receptor; Aggregates; Immune complexes

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APA (6th Edition):

Brachet, G. (2017). Déterminants moléculaires de la pharmacocinétique des anticorps thérapeutiques : Molecular determinants of monoclonal antibody pharmacokinetics. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2017TOUR3801

Chicago Manual of Style (16th Edition):

Brachet, Guillaume. “Déterminants moléculaires de la pharmacocinétique des anticorps thérapeutiques : Molecular determinants of monoclonal antibody pharmacokinetics.” 2017. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed July 16, 2019. http://www.theses.fr/2017TOUR3801.

MLA Handbook (7th Edition):

Brachet, Guillaume. “Déterminants moléculaires de la pharmacocinétique des anticorps thérapeutiques : Molecular determinants of monoclonal antibody pharmacokinetics.” 2017. Web. 16 Jul 2019.

Vancouver:

Brachet G. Déterminants moléculaires de la pharmacocinétique des anticorps thérapeutiques : Molecular determinants of monoclonal antibody pharmacokinetics. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2017. [cited 2019 Jul 16]. Available from: http://www.theses.fr/2017TOUR3801.

Council of Science Editors:

Brachet G. Déterminants moléculaires de la pharmacocinétique des anticorps thérapeutiques : Molecular determinants of monoclonal antibody pharmacokinetics. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2017. Available from: http://www.theses.fr/2017TOUR3801


Ryerson University

14. Dufresne, Jaimie. The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry.

Degree: 2017, Ryerson University

 Cell surface receptors are of critical importance to the treatment of disease but are difficult to isolate and identify by classical approaches. Here, a robust… (more)

Subjects/Keywords: Cell receptors; Cell membranes; Ligands; Fc receptors; Ligand binding (Biochemistry); Receptor-ligand complexes; Affinity chromatography; Liquid chromatography; Tandem mass spectometry

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APA (6th Edition):

Dufresne, J. (2017). The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A7225

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):

Dufresne, Jaimie. “The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry.” 2017. Thesis, Ryerson University. Accessed July 16, 2019. https://digital.library.ryerson.ca/islandora/object/RULA%3A7225.

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

MLA Handbook (7th Edition):

Dufresne, Jaimie. “The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry.” 2017. Web. 16 Jul 2019.

Vancouver:

Dufresne J. The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry. [Internet] [Thesis]. Ryerson University; 2017. [cited 2019 Jul 16]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A7225.

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

Council of Science Editors:

Dufresne J. The characterization of cell surface receptor complexes by affinity chromatography, liquid chromatography and tandem mass spectrometry. [Thesis]. Ryerson University; 2017. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A7225

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


Universitat de Barcelona

15. Guilabert Vidal, Antonio. Polimorfismos del receptor Fc gamma en patología cutánea inmunomediada: Papel en la patogenia del penfigoide ampolloso y en la respuesta a tratamiento biológico en la psoriasis.

Degree: 2012, Universitat de Barcelona

Fc gamma receptors (Fc-gammaR) mediate most of the immune functions of IgG. There are single-nucleotide polimorphims affecting Fc-gammaR genes that influence affinity and thus functions… (more)

Subjects/Keywords: Pefigoide ampolloso; Psoriasis; Receptor Fc gamma; Tratamiento biológico; Anti-TNF-alfa; Ciències de la Salut; 616.5

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APA (6th Edition):

Guilabert Vidal, A. (2012). Polimorfismos del receptor Fc gamma en patología cutánea inmunomediada: Papel en la patogenia del penfigoide ampolloso y en la respuesta a tratamiento biológico en la psoriasis. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/78982

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):

Guilabert Vidal, Antonio. “Polimorfismos del receptor Fc gamma en patología cutánea inmunomediada: Papel en la patogenia del penfigoide ampolloso y en la respuesta a tratamiento biológico en la psoriasis.” 2012. Thesis, Universitat de Barcelona. Accessed July 16, 2019. http://hdl.handle.net/10803/78982.

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

MLA Handbook (7th Edition):

Guilabert Vidal, Antonio. “Polimorfismos del receptor Fc gamma en patología cutánea inmunomediada: Papel en la patogenia del penfigoide ampolloso y en la respuesta a tratamiento biológico en la psoriasis.” 2012. Web. 16 Jul 2019.

Vancouver:

Guilabert Vidal A. Polimorfismos del receptor Fc gamma en patología cutánea inmunomediada: Papel en la patogenia del penfigoide ampolloso y en la respuesta a tratamiento biológico en la psoriasis. [Internet] [Thesis]. Universitat de Barcelona; 2012. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10803/78982.

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

Council of Science Editors:

Guilabert Vidal A. Polimorfismos del receptor Fc gamma en patología cutánea inmunomediada: Papel en la patogenia del penfigoide ampolloso y en la respuesta a tratamiento biológico en la psoriasis. [Thesis]. Universitat de Barcelona; 2012. Available from: http://hdl.handle.net/10803/78982

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


University of Kansas

16. Shah, Ishan Sanjeev. SITE-SPECIFIC GLYCOSYLATION ANALYSIS OF IgG3 AND THE EFFECT OF GLYCOSYLATION ON THE STRUCTURE, PHYSICAL STABILITY AND Fc RECEPTOR INTERACTIONS OF IgG3 Fc.

Degree: PhD, Pharmaceutical Chemistry, 2017, University of Kansas

 Therapeutic monoclonal antibodies based on the IgG class of antibodies are glycoproteins that contain glycosylation sites within their Fc region. Glycosylation is important for Fc-mediated… (more)

Subjects/Keywords: Pharmaceutical sciences; alpha 1; 2 mannosidase; Fc gamma receptor; FcRn; Man5; Pichia pastoris; X-ray crystal structure

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APA (6th Edition):

Shah, I. S. (2017). SITE-SPECIFIC GLYCOSYLATION ANALYSIS OF IgG3 AND THE EFFECT OF GLYCOSYLATION ON THE STRUCTURE, PHYSICAL STABILITY AND Fc RECEPTOR INTERACTIONS OF IgG3 Fc. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/25389

Chicago Manual of Style (16th Edition):

Shah, Ishan Sanjeev. “SITE-SPECIFIC GLYCOSYLATION ANALYSIS OF IgG3 AND THE EFFECT OF GLYCOSYLATION ON THE STRUCTURE, PHYSICAL STABILITY AND Fc RECEPTOR INTERACTIONS OF IgG3 Fc.” 2017. Doctoral Dissertation, University of Kansas. Accessed July 16, 2019. http://hdl.handle.net/1808/25389.

MLA Handbook (7th Edition):

Shah, Ishan Sanjeev. “SITE-SPECIFIC GLYCOSYLATION ANALYSIS OF IgG3 AND THE EFFECT OF GLYCOSYLATION ON THE STRUCTURE, PHYSICAL STABILITY AND Fc RECEPTOR INTERACTIONS OF IgG3 Fc.” 2017. Web. 16 Jul 2019.

Vancouver:

Shah IS. SITE-SPECIFIC GLYCOSYLATION ANALYSIS OF IgG3 AND THE EFFECT OF GLYCOSYLATION ON THE STRUCTURE, PHYSICAL STABILITY AND Fc RECEPTOR INTERACTIONS OF IgG3 Fc. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1808/25389.

Council of Science Editors:

Shah IS. SITE-SPECIFIC GLYCOSYLATION ANALYSIS OF IgG3 AND THE EFFECT OF GLYCOSYLATION ON THE STRUCTURE, PHYSICAL STABILITY AND Fc RECEPTOR INTERACTIONS OF IgG3 Fc. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/25389


University of Cambridge

17. Jing, Chenzhi. Characterisation of the effect and functional significance of Fcγ receptor crosslinking on metabolic processes in macrophages.

Degree: PhD, 2018, University of Cambridge

 The metabolic state of an immune cell directly influences its ability to function and differentiate, ultimately affecting immunity, inflammation and tolerance. Different immune cell subsets… (more)

Subjects/Keywords: Metabolism; Macrophages; Immune complex; Glycolysis; Cholesterol; Fc? receptor; Metabolic reprogramming; System lupus erythematosus; Cell migration; Interleukine-1ß

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APA (6th Edition):

Jing, C. (2018). Characterisation of the effect and functional significance of Fcγ receptor crosslinking on metabolic processes in macrophages. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/280316 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753486

Chicago Manual of Style (16th Edition):

Jing, Chenzhi. “Characterisation of the effect and functional significance of Fcγ receptor crosslinking on metabolic processes in macrophages.” 2018. Doctoral Dissertation, University of Cambridge. Accessed July 16, 2019. https://www.repository.cam.ac.uk/handle/1810/280316 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753486.

MLA Handbook (7th Edition):

Jing, Chenzhi. “Characterisation of the effect and functional significance of Fcγ receptor crosslinking on metabolic processes in macrophages.” 2018. Web. 16 Jul 2019.

Vancouver:

Jing C. Characterisation of the effect and functional significance of Fcγ receptor crosslinking on metabolic processes in macrophages. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Jul 16]. Available from: https://www.repository.cam.ac.uk/handle/1810/280316 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753486.

Council of Science Editors:

Jing C. Characterisation of the effect and functional significance of Fcγ receptor crosslinking on metabolic processes in macrophages. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/280316 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753486


Seton Hall University

18. Devenney, Kyle. Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection.

Degree: MS Biology, Biology, 2018, Seton Hall University

  Using a murine model, we have previously showed that targeting an inactivated form of F.tularensis (iFt) bacteria to Fcg receptors by utilizing an IgG2a,… (more)

Subjects/Keywords: T helper; Th17; Fc receptor; FcR-targeting; Francisella tularensis; vaccine development; Bacteriology; Cell Biology; Immunology of Infectious Disease

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APA (6th Edition):

Devenney, K. (2018). Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection. (Doctoral Dissertation). Seton Hall University. Retrieved from https://scholarship.shu.edu/dissertations/2588

Chicago Manual of Style (16th Edition):

Devenney, Kyle. “Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection.” 2018. Doctoral Dissertation, Seton Hall University. Accessed July 16, 2019. https://scholarship.shu.edu/dissertations/2588.

MLA Handbook (7th Edition):

Devenney, Kyle. “Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection.” 2018. Web. 16 Jul 2019.

Vancouver:

Devenney K. Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection. [Internet] [Doctoral dissertation]. Seton Hall University; 2018. [cited 2019 Jul 16]. Available from: https://scholarship.shu.edu/dissertations/2588.

Council of Science Editors:

Devenney K. Characterization of the Protective Role of Th17 Cells in an Fc Receptor-Targeted Vaccine Strategy Against Fracisella tularensis Infection. [Doctoral Dissertation]. Seton Hall University; 2018. Available from: https://scholarship.shu.edu/dissertations/2588

19. CHAN KUAN RONG. Molecular Insights into Neutralization and Enhancement of Dengue Virus Infection in Monocytes.

Degree: 2012, National University of Singapore

Subjects/Keywords: Dengue; Antibody; Neutralization; Enhancement; Monocyte; Fc receptor

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APA (6th Edition):

RONG, C. K. (2012). Molecular Insights into Neutralization and Enhancement of Dengue Virus Infection in Monocytes. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/36556

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):

RONG, CHAN KUAN. “Molecular Insights into Neutralization and Enhancement of Dengue Virus Infection in Monocytes.” 2012. Thesis, National University of Singapore. Accessed July 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/36556.

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

MLA Handbook (7th Edition):

RONG, CHAN KUAN. “Molecular Insights into Neutralization and Enhancement of Dengue Virus Infection in Monocytes.” 2012. Web. 16 Jul 2019.

Vancouver:

RONG CK. Molecular Insights into Neutralization and Enhancement of Dengue Virus Infection in Monocytes. [Internet] [Thesis]. National University of Singapore; 2012. [cited 2019 Jul 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/36556.

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

Council of Science Editors:

RONG CK. Molecular Insights into Neutralization and Enhancement of Dengue Virus Infection in Monocytes. [Thesis]. National University of Singapore; 2012. Available from: http://scholarbank.nus.edu.sg/handle/10635/36556

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


Universidad Nacional de La Plata

20. Garro, Adriana del Carmen. Estudio de la respuesta inmune humoral en la gestación porcina.

Degree: 2015, Universidad Nacional de La Plata

 La preñez en los mamíferos se atribuye a la regulación del sistema inmune materno por factores placentarios. En el presente trabajo de tesis se estudió… (more)

Subjects/Keywords: Ciencias Veterinarias; Mamíferos; Porcinos; Reproducción; cerdo; placenta; IgG; Ac IgG asimétricos; receptor Fc-gama de IgG

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APA (6th Edition):

Garro, A. d. C. (2015). Estudio de la respuesta inmune humoral en la gestación porcina. (Thesis). Universidad Nacional de La Plata. Retrieved from http://hdl.handle.net/10915/54668

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):

Garro, Adriana del Carmen. “Estudio de la respuesta inmune humoral en la gestación porcina.” 2015. Thesis, Universidad Nacional de La Plata. Accessed July 16, 2019. http://hdl.handle.net/10915/54668.

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

MLA Handbook (7th Edition):

Garro, Adriana del Carmen. “Estudio de la respuesta inmune humoral en la gestación porcina.” 2015. Web. 16 Jul 2019.

Vancouver:

Garro AdC. Estudio de la respuesta inmune humoral en la gestación porcina. [Internet] [Thesis]. Universidad Nacional de La Plata; 2015. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10915/54668.

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

Council of Science Editors:

Garro AdC. Estudio de la respuesta inmune humoral en la gestación porcina. [Thesis]. Universidad Nacional de La Plata; 2015. Available from: http://hdl.handle.net/10915/54668

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


Colorado State University

21. Chotiwan, Nunya. Molecular determinants of dengue virus type-2 critical for early events in antibody-dependent enhancement of infection.

Degree: MS(M.S.), Microbiology, Immunology, and Pathology, 2007, Colorado State University

 Antibody-dependent enhancement (ADE) of infection might be one of the major factors in the development of more severe forms of dengue disease in patients undergoing… (more)

Subjects/Keywords: antibody dependent enhancement; fc gamma receptor; envelope; dengue virus

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APA (6th Edition):

Chotiwan, N. (2007). Molecular determinants of dengue virus type-2 critical for early events in antibody-dependent enhancement of infection. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/80225

Chicago Manual of Style (16th Edition):

Chotiwan, Nunya. “Molecular determinants of dengue virus type-2 critical for early events in antibody-dependent enhancement of infection.” 2007. Masters Thesis, Colorado State University. Accessed July 16, 2019. http://hdl.handle.net/10217/80225.

MLA Handbook (7th Edition):

Chotiwan, Nunya. “Molecular determinants of dengue virus type-2 critical for early events in antibody-dependent enhancement of infection.” 2007. Web. 16 Jul 2019.

Vancouver:

Chotiwan N. Molecular determinants of dengue virus type-2 critical for early events in antibody-dependent enhancement of infection. [Internet] [Masters thesis]. Colorado State University; 2007. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10217/80225.

Council of Science Editors:

Chotiwan N. Molecular determinants of dengue virus type-2 critical for early events in antibody-dependent enhancement of infection. [Masters Thesis]. Colorado State University; 2007. Available from: http://hdl.handle.net/10217/80225


Queensland University of Technology

22. Armitage, Charles William. The role of immunoglobulins and their transporters in urogenital Chlamydial infections.

Degree: 2012, Queensland University of Technology

 Chlamydia trachomatis infections of the male and female reproductive tracts are the world's leading sexually transmitted bacterial disease, and can lead to damaging pathology, scarring… (more)

Subjects/Keywords: Chlamydia trachomatis; Chlamydia muridarum; immunoglobulin (Ig); IgG; IgA; neonatal Fc receptor (FcRn); polymeric immunoglobulin receptor (pIgR); reproductive tract; vaccine design; MOMP; IncA; CPAF

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APA (6th Edition):

Armitage, C. W. (2012). The role of immunoglobulins and their transporters in urogenital Chlamydial infections. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/63693/

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):

Armitage, Charles William. “The role of immunoglobulins and their transporters in urogenital Chlamydial infections.” 2012. Thesis, Queensland University of Technology. Accessed July 16, 2019. https://eprints.qut.edu.au/63693/.

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

MLA Handbook (7th Edition):

Armitage, Charles William. “The role of immunoglobulins and their transporters in urogenital Chlamydial infections.” 2012. Web. 16 Jul 2019.

Vancouver:

Armitage CW. The role of immunoglobulins and their transporters in urogenital Chlamydial infections. [Internet] [Thesis]. Queensland University of Technology; 2012. [cited 2019 Jul 16]. Available from: https://eprints.qut.edu.au/63693/.

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

Council of Science Editors:

Armitage CW. The role of immunoglobulins and their transporters in urogenital Chlamydial infections. [Thesis]. Queensland University of Technology; 2012. Available from: https://eprints.qut.edu.au/63693/

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


Brigham Young University

23. Zhou, Xueyuan. Follicular Dendritic Cells, Human Immunodeficency Virus Type 1, and Alpha 1 Antitrypsin.

Degree: PhD, 2012, Brigham Young University

  HIV/AIDS is raging and causing millions of deaths around the world. The major challenge in treating HIV/AIDS is the establishment of HIV reservoirs where… (more)

Subjects/Keywords: HIV replication; HIV infection; HIV reservoir; Tummor necrosis factor α; ; ; Type II Fc gamma receptor; Type II complement receptor; Biochemistry; Chemistry

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APA (6th Edition):

Zhou, X. (2012). Follicular Dendritic Cells, Human Immunodeficency Virus Type 1, and Alpha 1 Antitrypsin. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4406&context=etd

Chicago Manual of Style (16th Edition):

Zhou, Xueyuan. “Follicular Dendritic Cells, Human Immunodeficency Virus Type 1, and Alpha 1 Antitrypsin.” 2012. Doctoral Dissertation, Brigham Young University. Accessed July 16, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4406&context=etd.

MLA Handbook (7th Edition):

Zhou, Xueyuan. “Follicular Dendritic Cells, Human Immunodeficency Virus Type 1, and Alpha 1 Antitrypsin.” 2012. Web. 16 Jul 2019.

Vancouver:

Zhou X. Follicular Dendritic Cells, Human Immunodeficency Virus Type 1, and Alpha 1 Antitrypsin. [Internet] [Doctoral dissertation]. Brigham Young University; 2012. [cited 2019 Jul 16]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4406&context=etd.

Council of Science Editors:

Zhou X. Follicular Dendritic Cells, Human Immunodeficency Virus Type 1, and Alpha 1 Antitrypsin. [Doctoral Dissertation]. Brigham Young University; 2012. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4406&context=etd


Universiteit Utrecht

24. Lammerts van Bueren, Jeroen Jilles. Epidermal growth factor receptor-targeted antibody therapy - Mechanisms of action and modulators of therapeutic efficacy.

Degree: 2008, Universiteit Utrecht

 Cancer is an increasing disease in the world population, and in recent years there has been substantial interest in the development of novel therapeutic agents… (more)

Subjects/Keywords: Geneeskunde; Antibodies; Epidermal growth factor receptor; Antibody immunotherapy; Mechanism of action; Signal transduction; Fc receptors; Antibody-dependent cell-mediated cytotoxicity; Fucosylation; Mutations; Pharmacokinetics

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APA (6th Edition):

Lammerts van Bueren, J. J. (2008). Epidermal growth factor receptor-targeted antibody therapy - Mechanisms of action and modulators of therapeutic efficacy. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/26198

Chicago Manual of Style (16th Edition):

Lammerts van Bueren, Jeroen Jilles. “Epidermal growth factor receptor-targeted antibody therapy - Mechanisms of action and modulators of therapeutic efficacy.” 2008. Doctoral Dissertation, Universiteit Utrecht. Accessed July 16, 2019. http://dspace.library.uu.nl:8080/handle/1874/26198.

MLA Handbook (7th Edition):

Lammerts van Bueren, Jeroen Jilles. “Epidermal growth factor receptor-targeted antibody therapy - Mechanisms of action and modulators of therapeutic efficacy.” 2008. Web. 16 Jul 2019.

Vancouver:

Lammerts van Bueren JJ. Epidermal growth factor receptor-targeted antibody therapy - Mechanisms of action and modulators of therapeutic efficacy. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2008. [cited 2019 Jul 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/26198.

Council of Science Editors:

Lammerts van Bueren JJ. Epidermal growth factor receptor-targeted antibody therapy - Mechanisms of action and modulators of therapeutic efficacy. [Doctoral Dissertation]. Universiteit Utrecht; 2008. Available from: http://dspace.library.uu.nl:8080/handle/1874/26198


Georgia State University

25. Rogers, Kenneth Alton. Immunoglobulins and Immunoglobulin Fc Receptors in Nonhuman Primates Commonly Used in Biomedical Research.

Degree: PhD, Biology, 2006, Georgia State University

 Antibodies neutralize and eliminate pathogens, malignancies, and toxins by acting either alone or in association with Fc receptors which, once engaged, activate the elimination mechanisms… (more)

Subjects/Keywords: Immunoglobulin Fc receptor; therapeutic antibodies; animal models; humoral immunity; Biology

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APA (6th Edition):

Rogers, K. A. (2006). Immunoglobulins and Immunoglobulin Fc Receptors in Nonhuman Primates Commonly Used in Biomedical Research. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/6

Chicago Manual of Style (16th Edition):

Rogers, Kenneth Alton. “Immunoglobulins and Immunoglobulin Fc Receptors in Nonhuman Primates Commonly Used in Biomedical Research.” 2006. Doctoral Dissertation, Georgia State University. Accessed July 16, 2019. https://scholarworks.gsu.edu/biology_diss/6.

MLA Handbook (7th Edition):

Rogers, Kenneth Alton. “Immunoglobulins and Immunoglobulin Fc Receptors in Nonhuman Primates Commonly Used in Biomedical Research.” 2006. Web. 16 Jul 2019.

Vancouver:

Rogers KA. Immunoglobulins and Immunoglobulin Fc Receptors in Nonhuman Primates Commonly Used in Biomedical Research. [Internet] [Doctoral dissertation]. Georgia State University; 2006. [cited 2019 Jul 16]. Available from: https://scholarworks.gsu.edu/biology_diss/6.

Council of Science Editors:

Rogers KA. Immunoglobulins and Immunoglobulin Fc Receptors in Nonhuman Primates Commonly Used in Biomedical Research. [Doctoral Dissertation]. Georgia State University; 2006. Available from: https://scholarworks.gsu.edu/biology_diss/6

26. Fang, Yu. A study of the contribution of mast cells to vaccination - Regulatory functions of Fc gamma receptors.

Degree: 2013, University of Gothenburg / Göteborgs Universitet

 This thesis aimed to explore the regulatory roles of mast cells in vaccination. Mast cells have been increasingly recognized as important orchestrators of immune regulation… (more)

Subjects/Keywords: mast cell; vaccine; adjuvant; CTA1-DD; Fc gamma receptor; apoptosis

Page 1 Page 2

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APA (6th Edition):

Fang, Y. (2013). A study of the contribution of mast cells to vaccination - Regulatory functions of Fc gamma receptors. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/32946

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):

Fang, Yu. “A study of the contribution of mast cells to vaccination - Regulatory functions of Fc gamma receptors.” 2013. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed July 16, 2019. http://hdl.handle.net/2077/32946.

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

MLA Handbook (7th Edition):

Fang, Yu. “A study of the contribution of mast cells to vaccination - Regulatory functions of Fc gamma receptors.” 2013. Web. 16 Jul 2019.

Vancouver:

Fang Y. A study of the contribution of mast cells to vaccination - Regulatory functions of Fc gamma receptors. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2013. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/2077/32946.

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

Council of Science Editors:

Fang Y. A study of the contribution of mast cells to vaccination - Regulatory functions of Fc gamma receptors. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2013. Available from: http://hdl.handle.net/2077/32946

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

27. 佐久間, 良子. Food allergens are transferred intact across the rat blood-placental barrier in vivo : Food allergens are transferred intact across the rat blood-placental barrier in vivo; 食物性アレルゲンは妊娠ラットの血液胎盤関門を通過し、胎仔へ輸送される.

Degree: 博士, 2016, Nakamura Gakuen University / 中村学園大学

平成24年度

Subjects/Keywords: Placenta; Blood-placental barrier; Transcytosis; Neonatal Fc receptor (FcRn); Immunoglobulin G (IgG); Ovalbumin

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APA (6th Edition):

佐久間, . (2016). Food allergens are transferred intact across the rat blood-placental barrier in vivo : Food allergens are transferred intact across the rat blood-placental barrier in vivo; 食物性アレルゲンは妊娠ラットの血液胎盤関門を通過し、胎仔へ輸送される. (Thesis). Nakamura Gakuen University / 中村学園大学. Retrieved from http://id.nii.ac.jp/1094/00000535/

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):

佐久間, 良子. “Food allergens are transferred intact across the rat blood-placental barrier in vivo : Food allergens are transferred intact across the rat blood-placental barrier in vivo; 食物性アレルゲンは妊娠ラットの血液胎盤関門を通過し、胎仔へ輸送される.” 2016. Thesis, Nakamura Gakuen University / 中村学園大学. Accessed July 16, 2019. http://id.nii.ac.jp/1094/00000535/.

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

MLA Handbook (7th Edition):

佐久間, 良子. “Food allergens are transferred intact across the rat blood-placental barrier in vivo : Food allergens are transferred intact across the rat blood-placental barrier in vivo; 食物性アレルゲンは妊娠ラットの血液胎盤関門を通過し、胎仔へ輸送される.” 2016. Web. 16 Jul 2019.

Vancouver:

佐久間 . Food allergens are transferred intact across the rat blood-placental barrier in vivo : Food allergens are transferred intact across the rat blood-placental barrier in vivo; 食物性アレルゲンは妊娠ラットの血液胎盤関門を通過し、胎仔へ輸送される. [Internet] [Thesis]. Nakamura Gakuen University / 中村学園大学; 2016. [cited 2019 Jul 16]. Available from: http://id.nii.ac.jp/1094/00000535/.

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

Council of Science Editors:

佐久間 . Food allergens are transferred intact across the rat blood-placental barrier in vivo : Food allergens are transferred intact across the rat blood-placental barrier in vivo; 食物性アレルゲンは妊娠ラットの血液胎盤関門を通過し、胎仔へ輸送される. [Thesis]. Nakamura Gakuen University / 中村学園大学; 2016. Available from: http://id.nii.ac.jp/1094/00000535/

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

28. Limothai, Wararat. Challenges in the Pharmacokinetics of Therapeutic Proteins.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Tennessee Health Science Center

  Due to the complex structure and complicated disposition pattern of therapeutic macromolecules, their pharmacokinetic interpretation has many challenges. Two of these challenges were investigated… (more)

Subjects/Keywords: Bioavailability; FcRn; Neonatal Fc receptor; Ontogeny; Target-mediated drug disposition; TMDD; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Limothai, W. (2015). Challenges in the Pharmacokinetics of Therapeutic Proteins. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/396

Chicago Manual of Style (16th Edition):

Limothai, Wararat. “Challenges in the Pharmacokinetics of Therapeutic Proteins.” 2015. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed July 16, 2019. https://dc.uthsc.edu/dissertations/396.

MLA Handbook (7th Edition):

Limothai, Wararat. “Challenges in the Pharmacokinetics of Therapeutic Proteins.” 2015. Web. 16 Jul 2019.

Vancouver:

Limothai W. Challenges in the Pharmacokinetics of Therapeutic Proteins. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2015. [cited 2019 Jul 16]. Available from: https://dc.uthsc.edu/dissertations/396.

Council of Science Editors:

Limothai W. Challenges in the Pharmacokinetics of Therapeutic Proteins. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2015. Available from: https://dc.uthsc.edu/dissertations/396

29. Overdijk, M.B. Antibody therapy of cancer : Fc receptor-mediated mechanisms of action.

Degree: 2013, University Utrecht

 Cancer, a class of malignant diseases characterized by unregulated cell growth, is still a leading cause of death worldwide. The high specificity of antibodies combined… (more)

Subjects/Keywords: Antibody; Immunotherapy; Fc-gamma receptor; ADCC; ADCP; Apoptosis; Mouse xenograft model

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

APA (6th Edition):

Overdijk, M. B. (2013). Antibody therapy of cancer : Fc receptor-mediated mechanisms of action. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/286536 ; URN:NBN:NL:UI:10-1874-286536 ; urn:isbn:978-90-6464-716-1 ; URN:NBN:NL:UI:10-1874-286536 ; http://dspace.library.uu.nl/handle/1874/286536

Chicago Manual of Style (16th Edition):

Overdijk, M B. “Antibody therapy of cancer : Fc receptor-mediated mechanisms of action.” 2013. Doctoral Dissertation, University Utrecht. Accessed July 16, 2019. http://dspace.library.uu.nl/handle/1874/286536 ; URN:NBN:NL:UI:10-1874-286536 ; urn:isbn:978-90-6464-716-1 ; URN:NBN:NL:UI:10-1874-286536 ; http://dspace.library.uu.nl/handle/1874/286536.

MLA Handbook (7th Edition):

Overdijk, M B. “Antibody therapy of cancer : Fc receptor-mediated mechanisms of action.” 2013. Web. 16 Jul 2019.

Vancouver:

Overdijk MB. Antibody therapy of cancer : Fc receptor-mediated mechanisms of action. [Internet] [Doctoral dissertation]. University Utrecht; 2013. [cited 2019 Jul 16]. Available from: http://dspace.library.uu.nl/handle/1874/286536 ; URN:NBN:NL:UI:10-1874-286536 ; urn:isbn:978-90-6464-716-1 ; URN:NBN:NL:UI:10-1874-286536 ; http://dspace.library.uu.nl/handle/1874/286536.

Council of Science Editors:

Overdijk MB. Antibody therapy of cancer : Fc receptor-mediated mechanisms of action. [Doctoral Dissertation]. University Utrecht; 2013. Available from: http://dspace.library.uu.nl/handle/1874/286536 ; URN:NBN:NL:UI:10-1874-286536 ; urn:isbn:978-90-6464-716-1 ; URN:NBN:NL:UI:10-1874-286536 ; http://dspace.library.uu.nl/handle/1874/286536

30. Otten, Marielle Anna. Antibody therapeutic approaches for cancer.

Degree: 2006, University Utrecht

 FcalphaRI as target for antibody therapy: Anti-tumor antibodies are promising therapeutics for cancer. Currently, all FDA-approved therapeutic antibodies are of the IgG class, which interact… (more)

Subjects/Keywords: Fc receptor; antibody; FcalphaRI; FcgammaR; immunotherapy; neutrophil; dendritic cell; migration; tumor; liver metastases

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

APA (6th Edition):

Otten, M. A. (2006). Antibody therapeutic approaches for cancer. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/9465 ; URN:NBN:NL:UI:10-1874-9465 ; urn:isbn:90-8559-171-6 ; URN:NBN:NL:UI:10-1874-9465 ; http://dspace.library.uu.nl/handle/1874/9465

Chicago Manual of Style (16th Edition):

Otten, Marielle Anna. “Antibody therapeutic approaches for cancer.” 2006. Doctoral Dissertation, University Utrecht. Accessed July 16, 2019. http://dspace.library.uu.nl/handle/1874/9465 ; URN:NBN:NL:UI:10-1874-9465 ; urn:isbn:90-8559-171-6 ; URN:NBN:NL:UI:10-1874-9465 ; http://dspace.library.uu.nl/handle/1874/9465.

MLA Handbook (7th Edition):

Otten, Marielle Anna. “Antibody therapeutic approaches for cancer.” 2006. Web. 16 Jul 2019.

Vancouver:

Otten MA. Antibody therapeutic approaches for cancer. [Internet] [Doctoral dissertation]. University Utrecht; 2006. [cited 2019 Jul 16]. Available from: http://dspace.library.uu.nl/handle/1874/9465 ; URN:NBN:NL:UI:10-1874-9465 ; urn:isbn:90-8559-171-6 ; URN:NBN:NL:UI:10-1874-9465 ; http://dspace.library.uu.nl/handle/1874/9465.

Council of Science Editors:

Otten MA. Antibody therapeutic approaches for cancer. [Doctoral Dissertation]. University Utrecht; 2006. Available from: http://dspace.library.uu.nl/handle/1874/9465 ; URN:NBN:NL:UI:10-1874-9465 ; urn:isbn:90-8559-171-6 ; URN:NBN:NL:UI:10-1874-9465 ; http://dspace.library.uu.nl/handle/1874/9465

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