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You searched for subject:(Antibody). Showing records 1 – 30 of 1699 total matches.

[1] [2] [3] [4] [5] … [57]

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Texas A&M University

1. Kang, Jeffrey Che-Wei. Engineering Anti-HER2 Antibodies for Enhanced Therapeutic Potency.

Degree: PhD, Medical Sciences, 2018, Texas A&M University

 HER2-postive breast cancer constitutes approximately 25% of breast cancer patients and leads to a worse prognosis. Antibody therapy, such as the anti-HER2 antibody trastuzumab, is… (more)

Subjects/Keywords: Antibody engineering; antibody-drug conjugate; bispecific antibody

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APA (6th Edition):

Kang, J. C. (2018). Engineering Anti-HER2 Antibodies for Enhanced Therapeutic Potency. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/192053

Chicago Manual of Style (16th Edition):

Kang, Jeffrey Che-Wei. “Engineering Anti-HER2 Antibodies for Enhanced Therapeutic Potency.” 2018. Doctoral Dissertation, Texas A&M University. Accessed April 15, 2021. http://hdl.handle.net/1969.1/192053.

MLA Handbook (7th Edition):

Kang, Jeffrey Che-Wei. “Engineering Anti-HER2 Antibodies for Enhanced Therapeutic Potency.” 2018. Web. 15 Apr 2021.

Vancouver:

Kang JC. Engineering Anti-HER2 Antibodies for Enhanced Therapeutic Potency. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1969.1/192053.

Council of Science Editors:

Kang JC. Engineering Anti-HER2 Antibodies for Enhanced Therapeutic Potency. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/192053


Harvard University

2. Ding, Ruihua. A Microfluidic Platform for Rapid Isolation of Cells Based on Secretion of Antigen Specific Antibodies.

Degree: PhD, 2017, Harvard University

Droplet microfluidics provides compartmentalization of cells into picoliter-sized droplets, enabling economical, sensitive and massively parallel biological assays. Droplets can be actively manipulated for different applications.… (more)

Subjects/Keywords: Microfluidics; Antibody

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APA (6th Edition):

Ding, R. (2017). A Microfluidic Platform for Rapid Isolation of Cells Based on Secretion of Antigen Specific Antibodies. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061470

Chicago Manual of Style (16th Edition):

Ding, Ruihua. “A Microfluidic Platform for Rapid Isolation of Cells Based on Secretion of Antigen Specific Antibodies.” 2017. Doctoral Dissertation, Harvard University. Accessed April 15, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061470.

MLA Handbook (7th Edition):

Ding, Ruihua. “A Microfluidic Platform for Rapid Isolation of Cells Based on Secretion of Antigen Specific Antibodies.” 2017. Web. 15 Apr 2021.

Vancouver:

Ding R. A Microfluidic Platform for Rapid Isolation of Cells Based on Secretion of Antigen Specific Antibodies. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2021 Apr 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061470.

Council of Science Editors:

Ding R. A Microfluidic Platform for Rapid Isolation of Cells Based on Secretion of Antigen Specific Antibodies. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061470

3. Enck, Kevin Mason. Design of an In-House Insulin ELISA.

Degree: 2015, Wake Forest University

 Insulin is a hormone synthesized by beta cells in the pancreas. In order to quantify the amount of insulin produced by the beta cells, different… (more)

Subjects/Keywords: Antibody

…specifications. The bound reagents are “tagged” by a detection enzyme which is linked to an antibody… …antigen of interest, such as insulin, to the plate and then binding a primary antibody… …except a secondary antibody conjugated with the enzyme is bound to the primary antibody (… …primary antibody, therefore increasing signal amplification. It is also more versatile because… …many primary antibodies can be made in one species while using the same secondary antibody… 

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APA (6th Edition):

Enck, K. M. (2015). Design of an In-House Insulin ELISA. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/57427

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):

Enck, Kevin Mason. “Design of an In-House Insulin ELISA.” 2015. Thesis, Wake Forest University. Accessed April 15, 2021. http://hdl.handle.net/10339/57427.

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

MLA Handbook (7th Edition):

Enck, Kevin Mason. “Design of an In-House Insulin ELISA.” 2015. Web. 15 Apr 2021.

Vancouver:

Enck KM. Design of an In-House Insulin ELISA. [Internet] [Thesis]. Wake Forest University; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10339/57427.

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

Council of Science Editors:

Enck KM. Design of an In-House Insulin ELISA. [Thesis]. Wake Forest University; 2015. Available from: http://hdl.handle.net/10339/57427

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


University of Manitoba

4. Waruk, Jillian. The mapping and characterization of a novel binding site on HIV-1 gp120 for the broadly neutralizing monoclonal antibody IgG1 b12.

Degree: Medical Microbiology, 2011, University of Manitoba

 HIV infects target cells via fusion events following surface envelope glycoprotein binding to the CD4 receptor and a chemokine co-receptor. Despite the high sequence variability… (more)

Subjects/Keywords: HIV; antibody

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APA (6th Edition):

Waruk, J. (2011). The mapping and characterization of a novel binding site on HIV-1 gp120 for the broadly neutralizing monoclonal antibody IgG1 b12. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4992

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):

Waruk, Jillian. “The mapping and characterization of a novel binding site on HIV-1 gp120 for the broadly neutralizing monoclonal antibody IgG1 b12.” 2011. Thesis, University of Manitoba. Accessed April 15, 2021. http://hdl.handle.net/1993/4992.

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

MLA Handbook (7th Edition):

Waruk, Jillian. “The mapping and characterization of a novel binding site on HIV-1 gp120 for the broadly neutralizing monoclonal antibody IgG1 b12.” 2011. Web. 15 Apr 2021.

Vancouver:

Waruk J. The mapping and characterization of a novel binding site on HIV-1 gp120 for the broadly neutralizing monoclonal antibody IgG1 b12. [Internet] [Thesis]. University of Manitoba; 2011. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1993/4992.

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

Council of Science Editors:

Waruk J. The mapping and characterization of a novel binding site on HIV-1 gp120 for the broadly neutralizing monoclonal antibody IgG1 b12. [Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4992

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


University of Ottawa

5. D'Eall, Calvin. Antitumour Activity of a Hinge- and Fc-engineered Chimeric Heavy-chain Antibody .

Degree: 2015, University of Ottawa

 EG2-hFc is an ≈ 80 kDa chimeric heavy-chain antibody comprised of human IgG1 hinge and fragment crystallisable bivalently linked to EG2; a camelid-derived, heavy chain… (more)

Subjects/Keywords: Antibody; ADCC

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APA (6th Edition):

D'Eall, C. (2015). Antitumour Activity of a Hinge- and Fc-engineered Chimeric Heavy-chain Antibody . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32999

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):

D'Eall, Calvin. “Antitumour Activity of a Hinge- and Fc-engineered Chimeric Heavy-chain Antibody .” 2015. Thesis, University of Ottawa. Accessed April 15, 2021. http://hdl.handle.net/10393/32999.

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

MLA Handbook (7th Edition):

D'Eall, Calvin. “Antitumour Activity of a Hinge- and Fc-engineered Chimeric Heavy-chain Antibody .” 2015. Web. 15 Apr 2021.

Vancouver:

D'Eall C. Antitumour Activity of a Hinge- and Fc-engineered Chimeric Heavy-chain Antibody . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10393/32999.

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

Council of Science Editors:

D'Eall C. Antitumour Activity of a Hinge- and Fc-engineered Chimeric Heavy-chain Antibody . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32999

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

6. -3503-5102. Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus.

Degree: PhD, Cell and molecular biology, 2016, University of Texas – Austin

 All biological life lives under the constant threat of viral infection. From the earliest homo sapiens until now well into the 21st century, the destruction… (more)

Subjects/Keywords: Virus; Antibody

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APA (6th Edition):

-3503-5102. (2016). Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46638

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-3503-5102. “Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed April 15, 2021. http://hdl.handle.net/2152/46638.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-3503-5102. “Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus.” 2016. Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-3503-5102. Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152/46638.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-3503-5102. Host range trade-offs in new world Arenaviruses and discovery of antibodies against Ebola virus and Norovirus. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/46638

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Texas – Austin

7. Hung, Jessica Joy. Design of co-solute formulations for stable, highly concentrated monoclonal antibody solutions with low viscosity.

Degree: PhD, Chemical Engineering, 2018, University of Texas – Austin

 Highly concentrated (> 200 mg/mL) monoclonal antibody (mAb) formulations with low viscosities are strongly desired for subcutaneous drug delivery for the treatment of diseases such… (more)

Subjects/Keywords: Antibody; Viscosity

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APA (6th Edition):

Hung, J. J. (2018). Design of co-solute formulations for stable, highly concentrated monoclonal antibody solutions with low viscosity. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9543

Chicago Manual of Style (16th Edition):

Hung, Jessica Joy. “Design of co-solute formulations for stable, highly concentrated monoclonal antibody solutions with low viscosity.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed April 15, 2021. http://dx.doi.org/10.26153/tsw/9543.

MLA Handbook (7th Edition):

Hung, Jessica Joy. “Design of co-solute formulations for stable, highly concentrated monoclonal antibody solutions with low viscosity.” 2018. Web. 15 Apr 2021.

Vancouver:

Hung JJ. Design of co-solute formulations for stable, highly concentrated monoclonal antibody solutions with low viscosity. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2021 Apr 15]. Available from: http://dx.doi.org/10.26153/tsw/9543.

Council of Science Editors:

Hung JJ. Design of co-solute formulations for stable, highly concentrated monoclonal antibody solutions with low viscosity. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://dx.doi.org/10.26153/tsw/9543


University of Ottawa

8. Keklikian, Artine. Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library .

Degree: 2011, University of Ottawa

Antibody phage display technology mimics the natural immune system, and has been widely used for rapid isolation of single-domain antibodies (sdAbs) with various binding specificities… (more)

Subjects/Keywords: Antibody phage display; Single domain antibody; VL

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APA (6th Edition):

Keklikian, A. (2011). Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/20197

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):

Keklikian, Artine. “Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library .” 2011. Thesis, University of Ottawa. Accessed April 15, 2021. http://hdl.handle.net/10393/20197.

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

MLA Handbook (7th Edition):

Keklikian, Artine. “Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library .” 2011. Web. 15 Apr 2021.

Vancouver:

Keklikian A. Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10393/20197.

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

Council of Science Editors:

Keklikian A. Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/20197

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


University of Victoria

9. Blackler, Ryan J. Structural investigations into conformational diversity, polyspecificity, and binding mechanisms of near-germline antibodies.

Degree: Department of Biochemistry and Microbiology, 2016, University of Victoria

 The antibody response has evolved under constant pressure to recognize common pathogens and also remain adaptable to novel threats. Given the limited size of the… (more)

Subjects/Keywords: Antigen-antibody reactions; Bispecific antibodies; Antibody diversity

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APA (6th Edition):

Blackler, R. J. (2016). Structural investigations into conformational diversity, polyspecificity, and binding mechanisms of near-germline antibodies. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/7305

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):

Blackler, Ryan J. “Structural investigations into conformational diversity, polyspecificity, and binding mechanisms of near-germline antibodies.” 2016. Thesis, University of Victoria. Accessed April 15, 2021. http://hdl.handle.net/1828/7305.

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

MLA Handbook (7th Edition):

Blackler, Ryan J. “Structural investigations into conformational diversity, polyspecificity, and binding mechanisms of near-germline antibodies.” 2016. Web. 15 Apr 2021.

Vancouver:

Blackler RJ. Structural investigations into conformational diversity, polyspecificity, and binding mechanisms of near-germline antibodies. [Internet] [Thesis]. University of Victoria; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1828/7305.

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

Council of Science Editors:

Blackler RJ. Structural investigations into conformational diversity, polyspecificity, and binding mechanisms of near-germline antibodies. [Thesis]. University of Victoria; 2016. Available from: http://hdl.handle.net/1828/7305

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


Georgia Tech

10. Moretti, Leandro. Approaches to improve expression and specificity of an antibody probe against fibronectin.

Degree: MS, Mechanical Engineering, 2016, Georgia Tech

 Phage display is a convenient method to select proteins of interest based on binding affinity. The Barker lab recently used this technology to discover an… (more)

Subjects/Keywords: Fibrosis; scFv; Phage display; Antibody fragment; Antibody

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APA (6th Edition):

Moretti, L. (2016). Approaches to improve expression and specificity of an antibody probe against fibronectin. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59115

Chicago Manual of Style (16th Edition):

Moretti, Leandro. “Approaches to improve expression and specificity of an antibody probe against fibronectin.” 2016. Masters Thesis, Georgia Tech. Accessed April 15, 2021. http://hdl.handle.net/1853/59115.

MLA Handbook (7th Edition):

Moretti, Leandro. “Approaches to improve expression and specificity of an antibody probe against fibronectin.” 2016. Web. 15 Apr 2021.

Vancouver:

Moretti L. Approaches to improve expression and specificity of an antibody probe against fibronectin. [Internet] [Masters thesis]. Georgia Tech; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1853/59115.

Council of Science Editors:

Moretti L. Approaches to improve expression and specificity of an antibody probe against fibronectin. [Masters Thesis]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59115


Tulane University

11. Guha, Shantanu. The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets.

Degree: 2020, Tulane University

[email protected]

During the 2013-2016 West African outbreak, severe gastrointestinal symptoms were common in Ebola patients and associated with poor outcome. The efficient spread of Ebola… (more)

Subjects/Keywords: ebola; peptide; antibody

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APA (6th Edition):

Guha, S. (2020). The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:119728

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):

Guha, Shantanu. “The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets.” 2020. Thesis, Tulane University. Accessed April 15, 2021. https://digitallibrary.tulane.edu/islandora/object/tulane:119728.

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

MLA Handbook (7th Edition):

Guha, Shantanu. “The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets.” 2020. Web. 15 Apr 2021.

Vancouver:

Guha S. The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets. [Internet] [Thesis]. Tulane University; 2020. [cited 2021 Apr 15]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:119728.

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

Council of Science Editors:

Guha S. The Ebola virus delta-peptides are enterotoxic viroporins in vivo and potentially druggable targets. [Thesis]. Tulane University; 2020. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:119728

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


Tulane University

12. Jairo, Grace. Engineering recombinant antibodies for immunosensors: Incorporating peptide tags for gold nanoparticle binding and incorporating the 12F6 antibody in a lateral flow device for detection of uranium in groundwater.

Degree: 2018, Tulane University

[email protected]

Groundwater contamination due to the presence of uranium is a subject of concern since chronic exposure to uranium can lead to health problems such… (more)

Subjects/Keywords: Antibody; Uranium; Immunoassays

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APA (6th Edition):

Jairo, G. (2018). Engineering recombinant antibodies for immunosensors: Incorporating peptide tags for gold nanoparticle binding and incorporating the 12F6 antibody in a lateral flow device for detection of uranium in groundwater. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:87910

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):

Jairo, Grace. “Engineering recombinant antibodies for immunosensors: Incorporating peptide tags for gold nanoparticle binding and incorporating the 12F6 antibody in a lateral flow device for detection of uranium in groundwater.” 2018. Thesis, Tulane University. Accessed April 15, 2021. https://digitallibrary.tulane.edu/islandora/object/tulane:87910.

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

MLA Handbook (7th Edition):

Jairo, Grace. “Engineering recombinant antibodies for immunosensors: Incorporating peptide tags for gold nanoparticle binding and incorporating the 12F6 antibody in a lateral flow device for detection of uranium in groundwater.” 2018. Web. 15 Apr 2021.

Vancouver:

Jairo G. Engineering recombinant antibodies for immunosensors: Incorporating peptide tags for gold nanoparticle binding and incorporating the 12F6 antibody in a lateral flow device for detection of uranium in groundwater. [Internet] [Thesis]. Tulane University; 2018. [cited 2021 Apr 15]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:87910.

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

Council of Science Editors:

Jairo G. Engineering recombinant antibodies for immunosensors: Incorporating peptide tags for gold nanoparticle binding and incorporating the 12F6 antibody in a lateral flow device for detection of uranium in groundwater. [Thesis]. Tulane University; 2018. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:87910

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


University of Utah

13. Martins, Thomas Bernd. Analysis of antibody responses to streptococcal and tissue antigens in patients with acute rheumatic fever;.

Degree: MS;, Pathology;, 2007, University of Utah

 Acute Rheumatic Fever (ARF) is an autoimmune disease occurring in individuals following untreated group A streptococcal infection believed to be triggered by antibodies to bacterial… (more)

Subjects/Keywords: Antigen-Antibody Reactions

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APA (6th Edition):

Martins, T. B. (2007). Analysis of antibody responses to streptococcal and tissue antigens in patients with acute rheumatic fever;. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/323/rec/35

Chicago Manual of Style (16th Edition):

Martins, Thomas Bernd. “Analysis of antibody responses to streptococcal and tissue antigens in patients with acute rheumatic fever;.” 2007. Masters Thesis, University of Utah. Accessed April 15, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/323/rec/35.

MLA Handbook (7th Edition):

Martins, Thomas Bernd. “Analysis of antibody responses to streptococcal and tissue antigens in patients with acute rheumatic fever;.” 2007. Web. 15 Apr 2021.

Vancouver:

Martins TB. Analysis of antibody responses to streptococcal and tissue antigens in patients with acute rheumatic fever;. [Internet] [Masters thesis]. University of Utah; 2007. [cited 2021 Apr 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/323/rec/35.

Council of Science Editors:

Martins TB. Analysis of antibody responses to streptococcal and tissue antigens in patients with acute rheumatic fever;. [Masters Thesis]. University of Utah; 2007. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/323/rec/35


University of Alberta

14. Lak, Parnian. Arabinofuranoside–Antibody Interactions: A Case Study of Furanoside–Protein Binding.

Degree: PhD, Department of Chemistry, 2014, University of Alberta

 Carbohydrate–protein interactions play key roles in a range of biological processes. Noticeable advancements have been made in understanding the features associated with the recognition of… (more)

Subjects/Keywords: Furanoside; Antibody; Binding

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APA (6th Edition):

Lak, P. (2014). Arabinofuranoside–Antibody Interactions: A Case Study of Furanoside–Protein Binding. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cpr76f368k

Chicago Manual of Style (16th Edition):

Lak, Parnian. “Arabinofuranoside–Antibody Interactions: A Case Study of Furanoside–Protein Binding.” 2014. Doctoral Dissertation, University of Alberta. Accessed April 15, 2021. https://era.library.ualberta.ca/files/cpr76f368k.

MLA Handbook (7th Edition):

Lak, Parnian. “Arabinofuranoside–Antibody Interactions: A Case Study of Furanoside–Protein Binding.” 2014. Web. 15 Apr 2021.

Vancouver:

Lak P. Arabinofuranoside–Antibody Interactions: A Case Study of Furanoside–Protein Binding. [Internet] [Doctoral dissertation]. University of Alberta; 2014. [cited 2021 Apr 15]. Available from: https://era.library.ualberta.ca/files/cpr76f368k.

Council of Science Editors:

Lak P. Arabinofuranoside–Antibody Interactions: A Case Study of Furanoside–Protein Binding. [Doctoral Dissertation]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/cpr76f368k


University of Sydney

15. Gasiorowski, Robin. CD300f As A Novel Therapeutic Antibody Target For Acute Myeloid Leukaemia .

Degree: 2017, University of Sydney

 Current outcomes for patient with acute myeloid leukaemia (AML) are unsatisfactory, particularly for older patients where the median overall survival is less than six months.… (more)

Subjects/Keywords: AML; Antibody; CD300f

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APA (6th Edition):

Gasiorowski, R. (2017). CD300f As A Novel Therapeutic Antibody Target For Acute Myeloid Leukaemia . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17190

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):

Gasiorowski, Robin. “CD300f As A Novel Therapeutic Antibody Target For Acute Myeloid Leukaemia .” 2017. Thesis, University of Sydney. Accessed April 15, 2021. http://hdl.handle.net/2123/17190.

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

MLA Handbook (7th Edition):

Gasiorowski, Robin. “CD300f As A Novel Therapeutic Antibody Target For Acute Myeloid Leukaemia .” 2017. Web. 15 Apr 2021.

Vancouver:

Gasiorowski R. CD300f As A Novel Therapeutic Antibody Target For Acute Myeloid Leukaemia . [Internet] [Thesis]. University of Sydney; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2123/17190.

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

Council of Science Editors:

Gasiorowski R. CD300f As A Novel Therapeutic Antibody Target For Acute Myeloid Leukaemia . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17190

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


University of Texas – Austin

16. Hyun, Jeongmin. Design and engineering of epitope specific antibodies.

Degree: PhD, Cell and Molecular Biology, 2016, University of Texas – Austin

 The knowledge of three-dimensional structures of membrane proteins aids in structure-based drug design, since about 60% of approved drug targets are known as membrane proteins.… (more)

Subjects/Keywords: Antibody; Crystallization chaperone

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APA (6th Edition):

Hyun, J. (2016). Design and engineering of epitope specific antibodies. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68580

Chicago Manual of Style (16th Edition):

Hyun, Jeongmin. “Design and engineering of epitope specific antibodies.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed April 15, 2021. http://hdl.handle.net/2152/68580.

MLA Handbook (7th Edition):

Hyun, Jeongmin. “Design and engineering of epitope specific antibodies.” 2016. Web. 15 Apr 2021.

Vancouver:

Hyun J. Design and engineering of epitope specific antibodies. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152/68580.

Council of Science Editors:

Hyun J. Design and engineering of epitope specific antibodies. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68580


University of Cambridge

17. Peris, Daniela. In vitro diversification of chimeric human/chicken antibodies.

Degree: PhD, 2019, University of Cambridge

 Cells that constitutively diversify their immunoglobulin genes can be used for selection of novel antibodies and refining affinities and specificities of existing ones (Cumbers et… (more)

Subjects/Keywords: Antibodies; DT40 cells; Antibody engineering; Chimeric antibodies; Antibody evolution; human antibodies; Antibody diversification

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APA (6th Edition):

Peris, D. (2019). In vitro diversification of chimeric human/chicken antibodies. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293408

Chicago Manual of Style (16th Edition):

Peris, Daniela. “In vitro diversification of chimeric human/chicken antibodies.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 15, 2021. https://www.repository.cam.ac.uk/handle/1810/293408.

MLA Handbook (7th Edition):

Peris, Daniela. “In vitro diversification of chimeric human/chicken antibodies.” 2019. Web. 15 Apr 2021.

Vancouver:

Peris D. In vitro diversification of chimeric human/chicken antibodies. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Apr 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/293408.

Council of Science Editors:

Peris D. In vitro diversification of chimeric human/chicken antibodies. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293408


University of Pretoria

18. [No author]. A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome .

Degree: 2008, University of Pretoria

 Guillain Barré Syndrome in humans is characterised by ascending paralysis. It is often associated with preceding infections two to four weeks prior to nadir and… (more)

Subjects/Keywords: Antibody-antigen interactions; Antibodies; UCTD

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APA (6th Edition):

author], [. (2008). A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-04172008-111655/

Chicago Manual of Style (16th Edition):

author], [No. “A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome .” 2008. Masters Thesis, University of Pretoria. Accessed April 15, 2021. http://upetd.up.ac.za/thesis/available/etd-04172008-111655/.

MLA Handbook (7th Edition):

author], [No. “A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome .” 2008. Web. 15 Apr 2021.

Vancouver:

author] [. A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome . [Internet] [Masters thesis]. University of Pretoria; 2008. [cited 2021 Apr 15]. Available from: http://upetd.up.ac.za/thesis/available/etd-04172008-111655/.

Council of Science Editors:

author] [. A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome . [Masters Thesis]. University of Pretoria; 2008. Available from: http://upetd.up.ac.za/thesis/available/etd-04172008-111655/

19. 岩澤, 淳; イワサワ, アツシ. Radioimmunoassay with Heterologous Antibody (Hetero-Antibody RIA) : Utilization of Highly Cross-Reactive Antibody Present in Polyclonal Antiserum.

Degree: 博士(医学), 1992, Gunma University / 群馬大学

学位記番号:医博甲408

Subjects/Keywords: Radioimmunoassay; Antibody

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APA (6th Edition):

岩澤, 淳; イワサワ, . (1992). Radioimmunoassay with Heterologous Antibody (Hetero-Antibody RIA) : Utilization of Highly Cross-Reactive Antibody Present in Polyclonal Antiserum. (Thesis). Gunma University / 群馬大学. Retrieved from http://hdl.handle.net/10087/8278

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):

岩澤, 淳; イワサワ, アツシ. “Radioimmunoassay with Heterologous Antibody (Hetero-Antibody RIA) : Utilization of Highly Cross-Reactive Antibody Present in Polyclonal Antiserum.” 1992. Thesis, Gunma University / 群馬大学. Accessed April 15, 2021. http://hdl.handle.net/10087/8278.

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

MLA Handbook (7th Edition):

岩澤, 淳; イワサワ, アツシ. “Radioimmunoassay with Heterologous Antibody (Hetero-Antibody RIA) : Utilization of Highly Cross-Reactive Antibody Present in Polyclonal Antiserum.” 1992. Web. 15 Apr 2021.

Vancouver:

岩澤, 淳; イワサワ . Radioimmunoassay with Heterologous Antibody (Hetero-Antibody RIA) : Utilization of Highly Cross-Reactive Antibody Present in Polyclonal Antiserum. [Internet] [Thesis]. Gunma University / 群馬大学; 1992. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10087/8278.

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

Council of Science Editors:

岩澤, 淳; イワサワ . Radioimmunoassay with Heterologous Antibody (Hetero-Antibody RIA) : Utilization of Highly Cross-Reactive Antibody Present in Polyclonal Antiserum. [Thesis]. Gunma University / 群馬大学; 1992. Available from: http://hdl.handle.net/10087/8278

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


University of Utah

20. Beard, Michael Arthur. Comparative effects of immunoglobulins and immunoglobulin fragments on the immune response of rabbits;.

Degree: MS;, Biomedical Informatics;, 1970, University of Utah

 Immunosuppression by passive transfer of antibody has been extensively studied and has resulted in at least one practical human application. Human immunoglobulin G anti-Rho is… (more)

Subjects/Keywords: Antibody; Physiochemical

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APA (6th Edition):

Beard, M. A. (1970). Comparative effects of immunoglobulins and immunoglobulin fragments on the immune response of rabbits;. (Masters Thesis). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/298/rec/177

Chicago Manual of Style (16th Edition):

Beard, Michael Arthur. “Comparative effects of immunoglobulins and immunoglobulin fragments on the immune response of rabbits;.” 1970. Masters Thesis, University of Utah. Accessed April 15, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/298/rec/177.

MLA Handbook (7th Edition):

Beard, Michael Arthur. “Comparative effects of immunoglobulins and immunoglobulin fragments on the immune response of rabbits;.” 1970. Web. 15 Apr 2021.

Vancouver:

Beard MA. Comparative effects of immunoglobulins and immunoglobulin fragments on the immune response of rabbits;. [Internet] [Masters thesis]. University of Utah; 1970. [cited 2021 Apr 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/298/rec/177.

Council of Science Editors:

Beard MA. Comparative effects of immunoglobulins and immunoglobulin fragments on the immune response of rabbits;. [Masters Thesis]. University of Utah; 1970. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/298/rec/177


University of Rochester

21. Maldonado, Felix William Santiago. The Use of Recombinant Hemagglutinin Proteins in the Study of Vaccination Against Emergent Influenza Viruses.

Degree: PhD, 2012, University of Rochester

 The current model for influenza vaccine design and production is not adequate to respond against emergent strains with high rates of mortality. Recent evidence has… (more)

Subjects/Keywords: Influenza; Vaccination; Recombinant Hemagglutinin; Antibody

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APA (6th Edition):

Maldonado, F. W. S. (2012). The Use of Recombinant Hemagglutinin Proteins in the Study of Vaccination Against Emergent Influenza Viruses. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/19794

Chicago Manual of Style (16th Edition):

Maldonado, Felix William Santiago. “The Use of Recombinant Hemagglutinin Proteins in the Study of Vaccination Against Emergent Influenza Viruses.” 2012. Doctoral Dissertation, University of Rochester. Accessed April 15, 2021. http://hdl.handle.net/1802/19794.

MLA Handbook (7th Edition):

Maldonado, Felix William Santiago. “The Use of Recombinant Hemagglutinin Proteins in the Study of Vaccination Against Emergent Influenza Viruses.” 2012. Web. 15 Apr 2021.

Vancouver:

Maldonado FWS. The Use of Recombinant Hemagglutinin Proteins in the Study of Vaccination Against Emergent Influenza Viruses. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1802/19794.

Council of Science Editors:

Maldonado FWS. The Use of Recombinant Hemagglutinin Proteins in the Study of Vaccination Against Emergent Influenza Viruses. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/19794


San Jose State University

22. Juarez, Silvia. SIRPα linked rituximab antibody co-targets CD20 and CD47 permitting selective binding to dual antigen expressing tumor cells.

Degree: MS, Biological Sciences, 2014, San Jose State University

  CD47 is a cell surface protein overexpressed by many cancer cells, relative to normal cells, and it interacts with ligand SIRPα expressed by phagocytic… (more)

Subjects/Keywords: antibody; CD20; CD47; SIRP

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APA (6th Edition):

Juarez, S. (2014). SIRPα linked rituximab antibody co-targets CD20 and CD47 permitting selective binding to dual antigen expressing tumor cells. (Masters Thesis). San Jose State University. Retrieved from https://doi.org/10.31979/etd.g4bn-m2uc ; https://scholarworks.sjsu.edu/etd_theses/4498

Chicago Manual of Style (16th Edition):

Juarez, Silvia. “SIRPα linked rituximab antibody co-targets CD20 and CD47 permitting selective binding to dual antigen expressing tumor cells.” 2014. Masters Thesis, San Jose State University. Accessed April 15, 2021. https://doi.org/10.31979/etd.g4bn-m2uc ; https://scholarworks.sjsu.edu/etd_theses/4498.

MLA Handbook (7th Edition):

Juarez, Silvia. “SIRPα linked rituximab antibody co-targets CD20 and CD47 permitting selective binding to dual antigen expressing tumor cells.” 2014. Web. 15 Apr 2021.

Vancouver:

Juarez S. SIRPα linked rituximab antibody co-targets CD20 and CD47 permitting selective binding to dual antigen expressing tumor cells. [Internet] [Masters thesis]. San Jose State University; 2014. [cited 2021 Apr 15]. Available from: https://doi.org/10.31979/etd.g4bn-m2uc ; https://scholarworks.sjsu.edu/etd_theses/4498.

Council of Science Editors:

Juarez S. SIRPα linked rituximab antibody co-targets CD20 and CD47 permitting selective binding to dual antigen expressing tumor cells. [Masters Thesis]. San Jose State University; 2014. Available from: https://doi.org/10.31979/etd.g4bn-m2uc ; https://scholarworks.sjsu.edu/etd_theses/4498


University of Alberta

23. Chow, Aaron K.Y. A novel mouse model of acute antibody-mediated transplant rejection shows simultaneous complement activating and anti-inflammatory effects of donor specific IgG antibodies.

Degree: MS, Medical Sciences- Laboratory Medicine and Pathology, 2013, University of Alberta

 We developed a small animal model of pure antibody-mediated rejection (ABMR) by utilizing fully major histocompatibility complex (MHC) mismatched kidney allografts in mice. By examining… (more)

Subjects/Keywords: Transplantation; Antibody; Rejection; Kidney

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APA (6th Edition):

Chow, A. K. Y. (2013). A novel mouse model of acute antibody-mediated transplant rejection shows simultaneous complement activating and anti-inflammatory effects of donor specific IgG antibodies. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/ht24wk73f

Chicago Manual of Style (16th Edition):

Chow, Aaron K Y. “A novel mouse model of acute antibody-mediated transplant rejection shows simultaneous complement activating and anti-inflammatory effects of donor specific IgG antibodies.” 2013. Masters Thesis, University of Alberta. Accessed April 15, 2021. https://era.library.ualberta.ca/files/ht24wk73f.

MLA Handbook (7th Edition):

Chow, Aaron K Y. “A novel mouse model of acute antibody-mediated transplant rejection shows simultaneous complement activating and anti-inflammatory effects of donor specific IgG antibodies.” 2013. Web. 15 Apr 2021.

Vancouver:

Chow AKY. A novel mouse model of acute antibody-mediated transplant rejection shows simultaneous complement activating and anti-inflammatory effects of donor specific IgG antibodies. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2021 Apr 15]. Available from: https://era.library.ualberta.ca/files/ht24wk73f.

Council of Science Editors:

Chow AKY. A novel mouse model of acute antibody-mediated transplant rejection shows simultaneous complement activating and anti-inflammatory effects of donor specific IgG antibodies. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/ht24wk73f


Georgia Tech

24. Garimalla, Swetha N. Integrative immunotranscriptomic analysis of long-lived plasma cells.

Degree: PhD, Biology, 2019, Georgia Tech

 Long-lived plasma cells are a key component of serological memory encoded by the adaptive immune response. To date, prior studies of these cell types have… (more)

Subjects/Keywords: Plasma cells; Antibody secreting cells

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APA (6th Edition):

Garimalla, S. N. (2019). Integrative immunotranscriptomic analysis of long-lived plasma cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62642

Chicago Manual of Style (16th Edition):

Garimalla, Swetha N. “Integrative immunotranscriptomic analysis of long-lived plasma cells.” 2019. Doctoral Dissertation, Georgia Tech. Accessed April 15, 2021. http://hdl.handle.net/1853/62642.

MLA Handbook (7th Edition):

Garimalla, Swetha N. “Integrative immunotranscriptomic analysis of long-lived plasma cells.” 2019. Web. 15 Apr 2021.

Vancouver:

Garimalla SN. Integrative immunotranscriptomic analysis of long-lived plasma cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1853/62642.

Council of Science Editors:

Garimalla SN. Integrative immunotranscriptomic analysis of long-lived plasma cells. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/62642


McMaster University

25. Lindo, Carl Jr. CHARACTERIZATION OF AN ALPHA2-ANTIPLASMIN ANTIBODY.

Degree: MSMS, 2020, McMaster University

 Thrombotic disorders include myocardial infarction (MI), acute ischemic stroke (AIS) and venous thromboembolism (VTE), which encompasses pulmonary embolism (PE), and deep vein thrombosis (DVT). To… (more)

Subjects/Keywords: antibody; thrombosis; thrombolysis; alpha2-antiplasmin

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APA (6th Edition):

Lindo, C. J. (2020). CHARACTERIZATION OF AN ALPHA2-ANTIPLASMIN ANTIBODY. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/25487

Chicago Manual of Style (16th Edition):

Lindo, Carl Jr. “CHARACTERIZATION OF AN ALPHA2-ANTIPLASMIN ANTIBODY.” 2020. Masters Thesis, McMaster University. Accessed April 15, 2021. http://hdl.handle.net/11375/25487.

MLA Handbook (7th Edition):

Lindo, Carl Jr. “CHARACTERIZATION OF AN ALPHA2-ANTIPLASMIN ANTIBODY.” 2020. Web. 15 Apr 2021.

Vancouver:

Lindo CJ. CHARACTERIZATION OF AN ALPHA2-ANTIPLASMIN ANTIBODY. [Internet] [Masters thesis]. McMaster University; 2020. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11375/25487.

Council of Science Editors:

Lindo CJ. CHARACTERIZATION OF AN ALPHA2-ANTIPLASMIN ANTIBODY. [Masters Thesis]. McMaster University; 2020. Available from: http://hdl.handle.net/11375/25487


University of Pretoria

26. Van der Merwe, Hermanus Daniel. A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome.

Degree: MSc, Biochemistry, 2008, University of Pretoria

 Guillain Barré Syndrome in humans is characterised by ascending paralysis. It is often associated with preceding infections two to four weeks prior to nadir and… (more)

Subjects/Keywords: Antibody-antigen interactions; Antibodies; UCTD

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APA (6th Edition):

Van der Merwe, H. (2008). A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/23995

Chicago Manual of Style (16th Edition):

Van der Merwe, Hermanus. “A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome.” 2008. Masters Thesis, University of Pretoria. Accessed April 15, 2021. http://hdl.handle.net/2263/23995.

MLA Handbook (7th Edition):

Van der Merwe, Hermanus. “A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome.” 2008. Web. 15 Apr 2021.

Vancouver:

Van der Merwe H. A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome. [Internet] [Masters thesis]. University of Pretoria; 2008. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2263/23995.

Council of Science Editors:

Van der Merwe H. A resonant mirror biosensor approach to understand antibody-antigen interactions in Guillain Barré Syndrome. [Masters Thesis]. University of Pretoria; 2008. Available from: http://hdl.handle.net/2263/23995


University of Cape Town

27. Moyo, Thandeka. Role of envelope compactness and glycosylation in HIV-1 resistance to neutralising antibody responses.

Degree: Image, Division of Immunology, 2017, University of Cape Town

 Understanding the mechanisms used by HIV-1 to evade antibody neutralisation may contribute to the design of a high-coverage vaccine. This thesis explores the mechanism used… (more)

Subjects/Keywords: HIV-1; Antibody responses

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APA (6th Edition):

Moyo, T. (2017). Role of envelope compactness and glycosylation in HIV-1 resistance to neutralising antibody responses. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/26866

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):

Moyo, Thandeka. “Role of envelope compactness and glycosylation in HIV-1 resistance to neutralising antibody responses.” 2017. Thesis, University of Cape Town. Accessed April 15, 2021. http://hdl.handle.net/11427/26866.

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

MLA Handbook (7th Edition):

Moyo, Thandeka. “Role of envelope compactness and glycosylation in HIV-1 resistance to neutralising antibody responses.” 2017. Web. 15 Apr 2021.

Vancouver:

Moyo T. Role of envelope compactness and glycosylation in HIV-1 resistance to neutralising antibody responses. [Internet] [Thesis]. University of Cape Town; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11427/26866.

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

Council of Science Editors:

Moyo T. Role of envelope compactness and glycosylation in HIV-1 resistance to neutralising antibody responses. [Thesis]. University of Cape Town; 2017. Available from: http://hdl.handle.net/11427/26866

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


Harvard University

28. Dantzler, Kathleen W. Gametocyte-specific immunity provides a rationale for novel transmission blocking interventions in Plasmodium falciparum.

Degree: PhD, 2017, Harvard University

The recent decline in global malaria burden has stimulated a renewed interest in malaria elimination and eradication. Understanding the biology of malaria transmission and identifying… (more)

Subjects/Keywords: Plasmodium; gametocyte; antibody; antigen

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APA (6th Edition):

Dantzler, K. W. (2017). Gametocyte-specific immunity provides a rationale for novel transmission blocking interventions in Plasmodium falciparum. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41140235

Chicago Manual of Style (16th Edition):

Dantzler, Kathleen W. “Gametocyte-specific immunity provides a rationale for novel transmission blocking interventions in Plasmodium falciparum.” 2017. Doctoral Dissertation, Harvard University. Accessed April 15, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41140235.

MLA Handbook (7th Edition):

Dantzler, Kathleen W. “Gametocyte-specific immunity provides a rationale for novel transmission blocking interventions in Plasmodium falciparum.” 2017. Web. 15 Apr 2021.

Vancouver:

Dantzler KW. Gametocyte-specific immunity provides a rationale for novel transmission blocking interventions in Plasmodium falciparum. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2021 Apr 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41140235.

Council of Science Editors:

Dantzler KW. Gametocyte-specific immunity provides a rationale for novel transmission blocking interventions in Plasmodium falciparum. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41140235


University of Debrecen

29. Baba Adamu, Harira. Monoclonal antibodies in the treatment of colorectal cancer .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Monoclonal antibodies used in the treatment of colorectal cancer are young in the drug market.They include the anti-VEGF recombinant humanized antibodies; bevacizumab,aflibercept,ramucirumab and two anti-EGFRs;… (more)

Subjects/Keywords: monoclonal antibody

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APA (6th Edition):

Baba Adamu, H. (n.d.). Monoclonal antibodies in the treatment of colorectal cancer . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/218612

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Baba Adamu, Harira. “Monoclonal antibodies in the treatment of colorectal cancer .” Thesis, University of Debrecen. Accessed April 15, 2021. http://hdl.handle.net/2437/218612.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Baba Adamu, Harira. “Monoclonal antibodies in the treatment of colorectal cancer .” Web. 15 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Baba Adamu H. Monoclonal antibodies in the treatment of colorectal cancer . [Internet] [Thesis]. University of Debrecen; [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2437/218612.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Baba Adamu H. Monoclonal antibodies in the treatment of colorectal cancer . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/218612

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Cambridge

30. Walsh, Stephen. The Development of Divinyl-Heteroaryl Linkers for the Synthesis of Stable and Functional Antibody-Drug Conjugates.

Degree: PhD, 2020, University of Cambridge

Antibody-drug conjugates (ADCs) are a class of targeted therapeutics that utilise the exquisite selectivity of antibodies for membrane receptors to selectively deliver cytotoxic warheads to… (more)

Subjects/Keywords: Chemistry; antibody-drug conjugates; bioconjugation

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

APA (6th Edition):

Walsh, S. (2020). The Development of Divinyl-Heteroaryl Linkers for the Synthesis of Stable and Functional Antibody-Drug Conjugates. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/297916

Chicago Manual of Style (16th Edition):

Walsh, Stephen. “The Development of Divinyl-Heteroaryl Linkers for the Synthesis of Stable and Functional Antibody-Drug Conjugates.” 2020. Doctoral Dissertation, University of Cambridge. Accessed April 15, 2021. https://www.repository.cam.ac.uk/handle/1810/297916.

MLA Handbook (7th Edition):

Walsh, Stephen. “The Development of Divinyl-Heteroaryl Linkers for the Synthesis of Stable and Functional Antibody-Drug Conjugates.” 2020. Web. 15 Apr 2021.

Vancouver:

Walsh S. The Development of Divinyl-Heteroaryl Linkers for the Synthesis of Stable and Functional Antibody-Drug Conjugates. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 Apr 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/297916.

Council of Science Editors:

Walsh S. The Development of Divinyl-Heteroaryl Linkers for the Synthesis of Stable and Functional Antibody-Drug Conjugates. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/297916

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