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You searched for +publisher:"University of Kansas" +contributor:("Siahaan, Teruna"). Showing records 1 – 30 of 89 total matches.

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University of Kansas

1. Behymer, Matthew Mark. Inhibition of Cell Adhesion by Peptides Derived from the EC-4 Domain of E-Cadherin.

Degree: MS, Pharmaceutical Chemistry, 2015, University of Kansas

 The objective of this project was to evaluate the biological activity of peptides derived from the EC-4 domain of E-cadherin in inhibiting E-cadherin-mediated cell-cell adhesion.… (more)

Subjects/Keywords: Pharmaceutical sciences

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APA (6th Edition):

Behymer, M. M. (2015). Inhibition of Cell Adhesion by Peptides Derived from the EC-4 Domain of E-Cadherin. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21666

Chicago Manual of Style (16th Edition):

Behymer, Matthew Mark. “Inhibition of Cell Adhesion by Peptides Derived from the EC-4 Domain of E-Cadherin.” 2015. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21666.

MLA Handbook (7th Edition):

Behymer, Matthew Mark. “Inhibition of Cell Adhesion by Peptides Derived from the EC-4 Domain of E-Cadherin.” 2015. Web. 28 Sep 2020.

Vancouver:

Behymer MM. Inhibition of Cell Adhesion by Peptides Derived from the EC-4 Domain of E-Cadherin. [Internet] [Masters thesis]. University of Kansas; 2015. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21666.

Council of Science Editors:

Behymer MM. Inhibition of Cell Adhesion by Peptides Derived from the EC-4 Domain of E-Cadherin. [Masters Thesis]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/21666


University of Kansas

2. McNiff, Michaela L. Development of Biologics Using the claMP Tag: Influence of the claMP Tag on Half-life and Proteolytic Stability.

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

 Peptide and protein therapeutics encounter proteases at every stage of delivery, beginning at the site of administration and ending in the intracellular lysosomal compartment. An… (more)

Subjects/Keywords: Pharmaceutical sciences; Biochemistry; Chemistry; biologics; claMP Tag; molecular probe; proteolysis

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APA (6th Edition):

McNiff, M. L. (2017). Development of Biologics Using the claMP Tag: Influence of the claMP Tag on Half-life and Proteolytic Stability. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/25385

Chicago Manual of Style (16th Edition):

McNiff, Michaela L. “Development of Biologics Using the claMP Tag: Influence of the claMP Tag on Half-life and Proteolytic Stability.” 2017. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/25385.

MLA Handbook (7th Edition):

McNiff, Michaela L. “Development of Biologics Using the claMP Tag: Influence of the claMP Tag on Half-life and Proteolytic Stability.” 2017. Web. 28 Sep 2020.

Vancouver:

McNiff ML. Development of Biologics Using the claMP Tag: Influence of the claMP Tag on Half-life and Proteolytic Stability. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/25385.

Council of Science Editors:

McNiff ML. Development of Biologics Using the claMP Tag: Influence of the claMP Tag on Half-life and Proteolytic Stability. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/25385


University of Kansas

3. Stewart, John M. Synthesis and Characterization of MOG-IDAC and PLP-PEG-B7AP Molecules for Efficacy Evaluation in the EAE mouse model.

Degree: MS, Pharmaceutical Chemistry, 2012, University of Kansas

 Synthesis, Formulation, and In vivo Evaluation of MOG-PEG-IDAC and PLP-PEG-B7AP for Targeting APC to Suppress EAE John M. Stewart, Crisandra Wilkie, Barlas Buyuktimkin, Ahmed Badawi,… (more)

Subjects/Keywords: Pharmaceutical sciences; Immunology; EAE; Immunological synapse; Mog-idac; Plp-peg-b7ap

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APA (6th Edition):

Stewart, J. M. (2012). Synthesis and Characterization of MOG-IDAC and PLP-PEG-B7AP Molecules for Efficacy Evaluation in the EAE mouse model. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/12189

Chicago Manual of Style (16th Edition):

Stewart, John M. “Synthesis and Characterization of MOG-IDAC and PLP-PEG-B7AP Molecules for Efficacy Evaluation in the EAE mouse model.” 2012. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/12189.

MLA Handbook (7th Edition):

Stewart, John M. “Synthesis and Characterization of MOG-IDAC and PLP-PEG-B7AP Molecules for Efficacy Evaluation in the EAE mouse model.” 2012. Web. 28 Sep 2020.

Vancouver:

Stewart JM. Synthesis and Characterization of MOG-IDAC and PLP-PEG-B7AP Molecules for Efficacy Evaluation in the EAE mouse model. [Internet] [Masters thesis]. University of Kansas; 2012. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/12189.

Council of Science Editors:

Stewart JM. Synthesis and Characterization of MOG-IDAC and PLP-PEG-B7AP Molecules for Efficacy Evaluation in the EAE mouse model. [Masters Thesis]. University of Kansas; 2012. Available from: http://hdl.handle.net/1808/12189


University of Kansas

4. AlSalman, Mohammed Sulieman. Binding studies of E-Cadherin peptides to the EC1 domain of E-Cadherin.

Degree: MS, Pharmaceutical Chemistry, 2013, University of Kansas

 The blood brain barrier (BBB) is a key role in delivering medication to the brain; if the drug molecules can overcome this obstacle, many brain… (more)

Subjects/Keywords: Pharmaceutical sciences; Biochemistry

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APA (6th Edition):

AlSalman, M. S. (2013). Binding studies of E-Cadherin peptides to the EC1 domain of E-Cadherin. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21623

Chicago Manual of Style (16th Edition):

AlSalman, Mohammed Sulieman. “Binding studies of E-Cadherin peptides to the EC1 domain of E-Cadherin.” 2013. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21623.

MLA Handbook (7th Edition):

AlSalman, Mohammed Sulieman. “Binding studies of E-Cadherin peptides to the EC1 domain of E-Cadherin.” 2013. Web. 28 Sep 2020.

Vancouver:

AlSalman MS. Binding studies of E-Cadherin peptides to the EC1 domain of E-Cadherin. [Internet] [Masters thesis]. University of Kansas; 2013. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21623.

Council of Science Editors:

AlSalman MS. Binding studies of E-Cadherin peptides to the EC1 domain of E-Cadherin. [Masters Thesis]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/21623


University of Kansas

5. Morgan, Carrie Marie. Investigating Eutectic Mixtures for Poorly Soluble Compounds.

Degree: MS, Pharmaceutical Chemistry, 2014, University of Kansas

 Abstract Improving the solubility and changing the dissolution rate of the poorly soluble active pharmaceutical ingredients (API's) AMG 517, glipizide, and naproxen through the preparation… (more)

Subjects/Keywords: Pharmaceutical sciences; AMG 517; Eutectic Mixtures; glipizide; naproxen

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APA (6th Edition):

Morgan, C. M. (2014). Investigating Eutectic Mixtures for Poorly Soluble Compounds. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21635

Chicago Manual of Style (16th Edition):

Morgan, Carrie Marie. “Investigating Eutectic Mixtures for Poorly Soluble Compounds.” 2014. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21635.

MLA Handbook (7th Edition):

Morgan, Carrie Marie. “Investigating Eutectic Mixtures for Poorly Soluble Compounds.” 2014. Web. 28 Sep 2020.

Vancouver:

Morgan CM. Investigating Eutectic Mixtures for Poorly Soluble Compounds. [Internet] [Masters thesis]. University of Kansas; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21635.

Council of Science Editors:

Morgan CM. Investigating Eutectic Mixtures for Poorly Soluble Compounds. [Masters Thesis]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21635


University of Kansas

6. Farokhi, Elinaz. Determination of Binding Sites of Cadherin Peptides on the EC1 domain of E-cadherin using NMR Spectroscopy.

Degree: MS, Pharmaceutical Chemistry, 2014, University of Kansas

 The objective of this work is to evaluate the binding mechanisms of synthetic cadherin peptides (ADTC7, ADTC9 and cHAVc3) to the EC1 domain of human… (more)

Subjects/Keywords: Pharmaceutical sciences

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APA (6th Edition):

Farokhi, E. (2014). Determination of Binding Sites of Cadherin Peptides on the EC1 domain of E-cadherin using NMR Spectroscopy. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21641

Chicago Manual of Style (16th Edition):

Farokhi, Elinaz. “Determination of Binding Sites of Cadherin Peptides on the EC1 domain of E-cadherin using NMR Spectroscopy.” 2014. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21641.

MLA Handbook (7th Edition):

Farokhi, Elinaz. “Determination of Binding Sites of Cadherin Peptides on the EC1 domain of E-cadherin using NMR Spectroscopy.” 2014. Web. 28 Sep 2020.

Vancouver:

Farokhi E. Determination of Binding Sites of Cadherin Peptides on the EC1 domain of E-cadherin using NMR Spectroscopy. [Internet] [Masters thesis]. University of Kansas; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21641.

Council of Science Editors:

Farokhi E. Determination of Binding Sites of Cadherin Peptides on the EC1 domain of E-cadherin using NMR Spectroscopy. [Masters Thesis]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21641


University of Kansas

7. Hutchison, Kevin Michael. Role of Glycosylation of IL-1ra on its Binding to IL-1R1.

Degree: MS, Pharmaceutical Chemistry, 2015, University of Kansas

 Interleukin 1 (IL-1) is an inflammatory cytokine that helps the immune system fight disease. The inflammatory action of IL-1 is regulated by the naturally occurring… (more)

Subjects/Keywords: Pharmaceutical sciences

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APA (6th Edition):

Hutchison, K. M. (2015). Role of Glycosylation of IL-1ra on its Binding to IL-1R1. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21664

Chicago Manual of Style (16th Edition):

Hutchison, Kevin Michael. “Role of Glycosylation of IL-1ra on its Binding to IL-1R1.” 2015. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21664.

MLA Handbook (7th Edition):

Hutchison, Kevin Michael. “Role of Glycosylation of IL-1ra on its Binding to IL-1R1.” 2015. Web. 28 Sep 2020.

Vancouver:

Hutchison KM. Role of Glycosylation of IL-1ra on its Binding to IL-1R1. [Internet] [Masters thesis]. University of Kansas; 2015. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21664.

Council of Science Editors:

Hutchison KM. Role of Glycosylation of IL-1ra on its Binding to IL-1R1. [Masters Thesis]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/21664


University of Kansas

8. Moulder, Kenneth Ryan. Follicular delivery of a novel peptide therapeutic for the treatment of androgenic alopecia.

Degree: MS, Bioengineering, 2015, University of Kansas

 Androgenic alopecia (AGA), commonly known as pattern baldness, along with “loss of hair” following chemotherapy induced alopecia (CIA) are widespread maladies with treatments of little… (more)

Subjects/Keywords: Biomedical engineering; Pharmaceutical sciences

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APA (6th Edition):

Moulder, K. R. (2015). Follicular delivery of a novel peptide therapeutic for the treatment of androgenic alopecia. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/25631

Chicago Manual of Style (16th Edition):

Moulder, Kenneth Ryan. “Follicular delivery of a novel peptide therapeutic for the treatment of androgenic alopecia.” 2015. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/25631.

MLA Handbook (7th Edition):

Moulder, Kenneth Ryan. “Follicular delivery of a novel peptide therapeutic for the treatment of androgenic alopecia.” 2015. Web. 28 Sep 2020.

Vancouver:

Moulder KR. Follicular delivery of a novel peptide therapeutic for the treatment of androgenic alopecia. [Internet] [Masters thesis]. University of Kansas; 2015. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/25631.

Council of Science Editors:

Moulder KR. Follicular delivery of a novel peptide therapeutic for the treatment of androgenic alopecia. [Masters Thesis]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/25631


University of Kansas

9. Moulder, Kenneth Ryan. Development and biophysical characterization of a hyaluronic acid – vitamin E conjugate as a subcutaneous delivery platform.

Degree: PhD, Pharmaceutical Chemistry, 2019, University of Kansas

 The inherent properties of protein therapeutics (e.g. high molecular weight, charged, conformationally dependent) has historically limited their administration to parenteral routes which presents new challenges… (more)

Subjects/Keywords: Pharmaceutical sciences; Coversin; Hyaluronic acid; Nanogel; Vitamin E

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APA (6th Edition):

Moulder, K. R. (2019). Development and biophysical characterization of a hyaluronic acid – vitamin E conjugate as a subcutaneous delivery platform. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/29847

Chicago Manual of Style (16th Edition):

Moulder, Kenneth Ryan. “Development and biophysical characterization of a hyaluronic acid – vitamin E conjugate as a subcutaneous delivery platform.” 2019. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/29847.

MLA Handbook (7th Edition):

Moulder, Kenneth Ryan. “Development and biophysical characterization of a hyaluronic acid – vitamin E conjugate as a subcutaneous delivery platform.” 2019. Web. 28 Sep 2020.

Vancouver:

Moulder KR. Development and biophysical characterization of a hyaluronic acid – vitamin E conjugate as a subcutaneous delivery platform. [Internet] [Doctoral dissertation]. University of Kansas; 2019. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/29847.

Council of Science Editors:

Moulder KR. Development and biophysical characterization of a hyaluronic acid – vitamin E conjugate as a subcutaneous delivery platform. [Doctoral Dissertation]. University of Kansas; 2019. Available from: http://hdl.handle.net/1808/29847


University of Kansas

10. Thati, Sharadvi. Optimizing the Treatment of Experimental Autoimmune Encephalomyelitis via Pulmonary Delivery of Soluble Antigen Arrays.

Degree: PhD, Pharmaceutical Chemistry, 2016, University of Kansas

 Soluble antigen arrays (SAgAs) were used to treat experimental autoimmune encephalomyelitis (EAE), which is a mouse model for multiple sclerosis (MS). SAgAs offer a targeted… (more)

Subjects/Keywords: Pharmaceutical sciences; experimental autoimmune encephalomyelitis; hyaluronic acid; multiple sclerosis; tolerance induction

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APA (6th Edition):

Thati, S. (2016). Optimizing the Treatment of Experimental Autoimmune Encephalomyelitis via Pulmonary Delivery of Soluble Antigen Arrays. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21656

Chicago Manual of Style (16th Edition):

Thati, Sharadvi. “Optimizing the Treatment of Experimental Autoimmune Encephalomyelitis via Pulmonary Delivery of Soluble Antigen Arrays.” 2016. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21656.

MLA Handbook (7th Edition):

Thati, Sharadvi. “Optimizing the Treatment of Experimental Autoimmune Encephalomyelitis via Pulmonary Delivery of Soluble Antigen Arrays.” 2016. Web. 28 Sep 2020.

Vancouver:

Thati S. Optimizing the Treatment of Experimental Autoimmune Encephalomyelitis via Pulmonary Delivery of Soluble Antigen Arrays. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21656.

Council of Science Editors:

Thati S. Optimizing the Treatment of Experimental Autoimmune Encephalomyelitis via Pulmonary Delivery of Soluble Antigen Arrays. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/21656


University of Kansas

11. Hartwell, Brittany. Determining Cellular and Molecular Mechanisms of Multivalent Soluble Antigen Arrays that Contribute to Therapeutic Efficacy Against a Murine Model of Multiple Sclerosis.

Degree: PhD, Bioengineering, 2016, University of Kansas

 A pressing need exists for antigen-specific immunotherapies (ASIT) that induce selective tolerance in autoimmune disease while avoiding deleterious global immunosuppression. Multivalent soluble antigen arrays (SAgAPLP:LABL),… (more)

Subjects/Keywords: Biomedical engineering; Immunology; Pharmaceutical sciences; antigen-specific immunotherapy; autoimmunity; B cell anergy; multivalent; nanomaterial; soluble antigen array

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APA (6th Edition):

Hartwell, B. (2016). Determining Cellular and Molecular Mechanisms of Multivalent Soluble Antigen Arrays that Contribute to Therapeutic Efficacy Against a Murine Model of Multiple Sclerosis. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/24140

Chicago Manual of Style (16th Edition):

Hartwell, Brittany. “Determining Cellular and Molecular Mechanisms of Multivalent Soluble Antigen Arrays that Contribute to Therapeutic Efficacy Against a Murine Model of Multiple Sclerosis.” 2016. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/24140.

MLA Handbook (7th Edition):

Hartwell, Brittany. “Determining Cellular and Molecular Mechanisms of Multivalent Soluble Antigen Arrays that Contribute to Therapeutic Efficacy Against a Murine Model of Multiple Sclerosis.” 2016. Web. 28 Sep 2020.

Vancouver:

Hartwell B. Determining Cellular and Molecular Mechanisms of Multivalent Soluble Antigen Arrays that Contribute to Therapeutic Efficacy Against a Murine Model of Multiple Sclerosis. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/24140.

Council of Science Editors:

Hartwell B. Determining Cellular and Molecular Mechanisms of Multivalent Soluble Antigen Arrays that Contribute to Therapeutic Efficacy Against a Murine Model of Multiple Sclerosis. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/24140

12. Northrup, Laura Ann. Co-Delivery of Immunomodulators and Autoantigen as Antigen-Specific Immunotherapy for the Treatment of a Murine Model of Multiple Sclerosis.

Degree: PhD, Pharmaceutical Chemistry, 2016, University of Kansas

 Multiple Sclerosis (MS) is an autoimmune disease characterized by the breakdown of immune tolerance towards autoantigen in the myelin sheath surrounding the neurons. Current therapies… (more)

Subjects/Keywords: Pharmaceutical sciences; Immunology; Biomedical engineering; antigen-specific immunotherapy; co-delivery; experimental autoimmune encephalomyelitis; multiple sclerosis

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APA (6th Edition):

Northrup, L. A. (2016). Co-Delivery of Immunomodulators and Autoantigen as Antigen-Specific Immunotherapy for the Treatment of a Murine Model of Multiple Sclerosis. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/24147

Chicago Manual of Style (16th Edition):

Northrup, Laura Ann. “Co-Delivery of Immunomodulators and Autoantigen as Antigen-Specific Immunotherapy for the Treatment of a Murine Model of Multiple Sclerosis.” 2016. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/24147.

MLA Handbook (7th Edition):

Northrup, Laura Ann. “Co-Delivery of Immunomodulators and Autoantigen as Antigen-Specific Immunotherapy for the Treatment of a Murine Model of Multiple Sclerosis.” 2016. Web. 28 Sep 2020.

Vancouver:

Northrup LA. Co-Delivery of Immunomodulators and Autoantigen as Antigen-Specific Immunotherapy for the Treatment of a Murine Model of Multiple Sclerosis. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/24147.

Council of Science Editors:

Northrup LA. Co-Delivery of Immunomodulators and Autoantigen as Antigen-Specific Immunotherapy for the Treatment of a Murine Model of Multiple Sclerosis. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/24147


University of Kansas

13. Johnson, Ryan Tyler. Advances and Applications of Capillary Electrophoresis-Mass Spectrometry.

Degree: PhD, Chemistry, 2016, University of Kansas

 Capillary electrophoresis-mass spectrometry (CE-MS) is a useful analytical technique capable of high efficiency separations from complex and low volume samples. However, the interface between CE… (more)

Subjects/Keywords: Analytical chemistry; Biochemistry; Capillary Electrophoresis; Eicosanoids; Flavonoids; Interface; Mass Spectrometry; Sheathless

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APA (6th Edition):

Johnson, R. T. (2016). Advances and Applications of Capillary Electrophoresis-Mass Spectrometry. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/24202

Chicago Manual of Style (16th Edition):

Johnson, Ryan Tyler. “Advances and Applications of Capillary Electrophoresis-Mass Spectrometry.” 2016. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/24202.

MLA Handbook (7th Edition):

Johnson, Ryan Tyler. “Advances and Applications of Capillary Electrophoresis-Mass Spectrometry.” 2016. Web. 28 Sep 2020.

Vancouver:

Johnson RT. Advances and Applications of Capillary Electrophoresis-Mass Spectrometry. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/24202.

Council of Science Editors:

Johnson RT. Advances and Applications of Capillary Electrophoresis-Mass Spectrometry. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/24202

14. Napolitano, Lorena Rodriguez Antunez. Adjuvant Interactions with Lipid Membranes and Their Effect on Cellular Immune Responses.

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

 Adjuvants are commonly included in vaccines and have been invaluable in making them safer and more robust. Despite their prolific use, adjuvant mechanisms of action… (more)

Subjects/Keywords: Pharmaceutical sciences; Adjuvant; Drug Delivery; Immunotherapy; Lipids; Mechanism of action; Membrane

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APA (6th Edition):

Napolitano, L. R. A. (2017). Adjuvant Interactions with Lipid Membranes and Their Effect on Cellular Immune Responses. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26152

Chicago Manual of Style (16th Edition):

Napolitano, Lorena Rodriguez Antunez. “Adjuvant Interactions with Lipid Membranes and Their Effect on Cellular Immune Responses.” 2017. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/26152.

MLA Handbook (7th Edition):

Napolitano, Lorena Rodriguez Antunez. “Adjuvant Interactions with Lipid Membranes and Their Effect on Cellular Immune Responses.” 2017. Web. 28 Sep 2020.

Vancouver:

Napolitano LRA. Adjuvant Interactions with Lipid Membranes and Their Effect on Cellular Immune Responses. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/26152.

Council of Science Editors:

Napolitano LRA. Adjuvant Interactions with Lipid Membranes and Their Effect on Cellular Immune Responses. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26152


University of Kansas

15. Imaduwage, Kasun Prabodha. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.

Degree: PhD, Chemistry, 2017, University of Kansas

 Developing effective high throughput screening (HTS) methods is of paramount importance in the early stage of drug discovery. When a protein binding event can be… (more)

Subjects/Keywords: Chemistry; false negatives; false positives; High throughput screening; LC/MS; library compounds; Target protein

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APA (6th Edition):

Imaduwage, K. P. (2017). High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26012

Chicago Manual of Style (16th Edition):

Imaduwage, Kasun Prabodha. “High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.” 2017. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/26012.

MLA Handbook (7th Edition):

Imaduwage, Kasun Prabodha. “High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS.” 2017. Web. 28 Sep 2020.

Vancouver:

Imaduwage KP. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/26012.

Council of Science Editors:

Imaduwage KP. High-Throughput Screening (HTS) of Potential Lead Compounds for Target Proteins with No False Identifications Using LC/MS. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26012


University of Kansas

16. Al-Kinani, Khalid Kadhem Abed. Modifying the Fc Asn297 Glycan of Human IgG2 Subclass for Improved Antibody Therapeutics and Design of Site-Specific Antibody Drug Conjugates.

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

 Immunoglobulin G (IgG) is a complex glycoprotein that is largely being used in the development of antibody-based therapeutics to treat a variety of diseases such… (more)

Subjects/Keywords: Pharmaceutical sciences; Antibody; Chemoenzymatic synthesis; Fucosylation; FUT8; Glycosylation; Site-Specific ADC

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APA (6th Edition):

Al-Kinani, K. K. A. (2017). Modifying the Fc Asn297 Glycan of Human IgG2 Subclass for Improved Antibody Therapeutics and Design of Site-Specific Antibody Drug Conjugates. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/25383

Chicago Manual of Style (16th Edition):

Al-Kinani, Khalid Kadhem Abed. “Modifying the Fc Asn297 Glycan of Human IgG2 Subclass for Improved Antibody Therapeutics and Design of Site-Specific Antibody Drug Conjugates.” 2017. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/25383.

MLA Handbook (7th Edition):

Al-Kinani, Khalid Kadhem Abed. “Modifying the Fc Asn297 Glycan of Human IgG2 Subclass for Improved Antibody Therapeutics and Design of Site-Specific Antibody Drug Conjugates.” 2017. Web. 28 Sep 2020.

Vancouver:

Al-Kinani KKA. Modifying the Fc Asn297 Glycan of Human IgG2 Subclass for Improved Antibody Therapeutics and Design of Site-Specific Antibody Drug Conjugates. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/25383.

Council of Science Editors:

Al-Kinani KKA. Modifying the Fc Asn297 Glycan of Human IgG2 Subclass for Improved Antibody Therapeutics and Design of Site-Specific Antibody Drug Conjugates. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/25383


University of Kansas

17. Hunt, Jordan Robert. Investigation of the Phenyl Ring of Imidazoquinolines.

Degree: MS, Medicinal Chemistry, 2018, University of Kansas

 The 1H-Imidazo-[4,5-c]quinolines are a class of compounds that are agonists towards Toll-like receptor 7 and 8 (TLR7/8). For example, Imiquimod and Resiquimod have been shown… (more)

Subjects/Keywords: Organic chemistry; Immunology; Adjuvants; Imidazoquinolines; Structure Activity Relationship; Toll-like Receptor 7; Vaccines

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APA (6th Edition):

Hunt, J. R. (2018). Investigation of the Phenyl Ring of Imidazoquinolines. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/29315

Chicago Manual of Style (16th Edition):

Hunt, Jordan Robert. “Investigation of the Phenyl Ring of Imidazoquinolines.” 2018. Masters Thesis, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/29315.

MLA Handbook (7th Edition):

Hunt, Jordan Robert. “Investigation of the Phenyl Ring of Imidazoquinolines.” 2018. Web. 28 Sep 2020.

Vancouver:

Hunt JR. Investigation of the Phenyl Ring of Imidazoquinolines. [Internet] [Masters thesis]. University of Kansas; 2018. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/29315.

Council of Science Editors:

Hunt JR. Investigation of the Phenyl Ring of Imidazoquinolines. [Masters Thesis]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/29315


University of Kansas

18. Shukla, Nikunj M. Modulators of Toll-like Receptors -7 and -8.

Degree: PhD, Medicinal Chemistry, 2011, University of Kansas

 Toll-like receptors (TLR)-7/-8 are innate immune receptors present in the endosomal compartment that are activated by single-stranded RNA (ssRNA) molecules of viral as well as… (more)

Subjects/Keywords: Pharmaceutical sciences; Immunology; Adjuvant; Autoimmune diseases; Hiv; Imidazoquinoline; Toll-like receptors; Vaccine

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APA (6th Edition):

Shukla, N. M. (2011). Modulators of Toll-like Receptors -7 and -8. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/8186

Chicago Manual of Style (16th Edition):

Shukla, Nikunj M. “Modulators of Toll-like Receptors -7 and -8.” 2011. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/8186.

MLA Handbook (7th Edition):

Shukla, Nikunj M. “Modulators of Toll-like Receptors -7 and -8.” 2011. Web. 28 Sep 2020.

Vancouver:

Shukla NM. Modulators of Toll-like Receptors -7 and -8. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/8186.

Council of Science Editors:

Shukla NM. Modulators of Toll-like Receptors -7 and -8. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/8186


University of Kansas

19. Krause, Mary Elizabeth. Structure/Function Relationships in Nickel-Peptide Complexes: Impact of the Primary Coordination Sphere on Square-Planar Nickel Chemistry.

Degree: PhD, Chemistry, 2011, University of Kansas

 The novel metal-binding tripeptide asparagine-cysteine-cysteine (NCC) is capable of coordinating a metal ion, and we are exploring its use in several biological applications. Different metals… (more)

Subjects/Keywords: Chemistry; Biochemistry; Inorganic chemistry; Chiral inversion; Metal abstraction peptide; Nickel; Ni-ncc; Peptide-metal complex; Square-planar

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APA (6th Edition):

Krause, M. E. (2011). Structure/Function Relationships in Nickel-Peptide Complexes: Impact of the Primary Coordination Sphere on Square-Planar Nickel Chemistry. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/10428

Chicago Manual of Style (16th Edition):

Krause, Mary Elizabeth. “Structure/Function Relationships in Nickel-Peptide Complexes: Impact of the Primary Coordination Sphere on Square-Planar Nickel Chemistry.” 2011. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/10428.

MLA Handbook (7th Edition):

Krause, Mary Elizabeth. “Structure/Function Relationships in Nickel-Peptide Complexes: Impact of the Primary Coordination Sphere on Square-Planar Nickel Chemistry.” 2011. Web. 28 Sep 2020.

Vancouver:

Krause ME. Structure/Function Relationships in Nickel-Peptide Complexes: Impact of the Primary Coordination Sphere on Square-Planar Nickel Chemistry. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/10428.

Council of Science Editors:

Krause ME. Structure/Function Relationships in Nickel-Peptide Complexes: Impact of the Primary Coordination Sphere on Square-Planar Nickel Chemistry. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/10428


University of Kansas

20. Cai, Shuang. Development of lymphatic drug delivery platforms for the treatment of carcinomas.

Degree: PhD, Pharmaceutical Chemistry, 2011, University of Kansas

 Many cancers, such as breast cancer, lung cancer, and head and neck cancer, preferentially metastasize via the lymphatic system prior to their systemic invasion. Conventional… (more)

Subjects/Keywords: Oncology; Cancer; Chemotherapy; Drug delivery; Lymphatic system; Nanotechnology; Polymer

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APA (6th Edition):

Cai, S. (2011). Development of lymphatic drug delivery platforms for the treatment of carcinomas. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/10703

Chicago Manual of Style (16th Edition):

Cai, Shuang. “Development of lymphatic drug delivery platforms for the treatment of carcinomas.” 2011. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/10703.

MLA Handbook (7th Edition):

Cai, Shuang. “Development of lymphatic drug delivery platforms for the treatment of carcinomas.” 2011. Web. 28 Sep 2020.

Vancouver:

Cai S. Development of lymphatic drug delivery platforms for the treatment of carcinomas. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/10703.

Council of Science Editors:

Cai S. Development of lymphatic drug delivery platforms for the treatment of carcinomas. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/10703


University of Kansas

21. Joshi, Anand Anant. Synthesis and biological evaluation of dynorphin analogs and, Caco-2 permeability of opioid macrocyclic tetrapeptides.

Degree: PhD, Medicinal Chemistry, 2013, University of Kansas

 We are interested in the development of potent and highly selective dynorphin (Dyn) analogs targeting kappa opioid receptors (KOR) and studying the pharmacokinetic and physicochemical… (more)

Subjects/Keywords: Pharmaceutical sciences; Caco-2; Dynorphins; Kappa opioid receptors; Macrocyclic tetrapeptides; Sar; Zyklophin

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APA (6th Edition):

Joshi, A. A. (2013). Synthesis and biological evaluation of dynorphin analogs and, Caco-2 permeability of opioid macrocyclic tetrapeptides. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/14842

Chicago Manual of Style (16th Edition):

Joshi, Anand Anant. “Synthesis and biological evaluation of dynorphin analogs and, Caco-2 permeability of opioid macrocyclic tetrapeptides.” 2013. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/14842.

MLA Handbook (7th Edition):

Joshi, Anand Anant. “Synthesis and biological evaluation of dynorphin analogs and, Caco-2 permeability of opioid macrocyclic tetrapeptides.” 2013. Web. 28 Sep 2020.

Vancouver:

Joshi AA. Synthesis and biological evaluation of dynorphin analogs and, Caco-2 permeability of opioid macrocyclic tetrapeptides. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/14842.

Council of Science Editors:

Joshi AA. Synthesis and biological evaluation of dynorphin analogs and, Caco-2 permeability of opioid macrocyclic tetrapeptides. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/14842


University of Kansas

22. Thomas, Justin Cody. Toward the Development of an Improved Ricin Vaccine.

Degree: PhD, Pharmaceutical Chemistry, 2013, University of Kansas

 To date, there is no approved antidote to treat or prevent the toxic effects of ricin exposure. RiVax, a recombinant ricin A chain subunit vaccine… (more)

Subjects/Keywords: Pharmaceutical sciences; antibodies; antigen; mutagenesis; protein stability; ricin toxin; vaccines

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APA (6th Edition):

Thomas, J. C. (2013). Toward the Development of an Improved Ricin Vaccine. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21628

Chicago Manual of Style (16th Edition):

Thomas, Justin Cody. “Toward the Development of an Improved Ricin Vaccine.” 2013. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21628.

MLA Handbook (7th Edition):

Thomas, Justin Cody. “Toward the Development of an Improved Ricin Vaccine.” 2013. Web. 28 Sep 2020.

Vancouver:

Thomas JC. Toward the Development of an Improved Ricin Vaccine. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21628.

Council of Science Editors:

Thomas JC. Toward the Development of an Improved Ricin Vaccine. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/21628


University of Kansas

23. Logan, Randall. Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function.

Degree: PhD, Pharmaceutical Chemistry, 2013, University of Kansas

 From a clinical perspective, a drug's pharmacokinetic properties (e.g., the volume of distribution, clearance, and half-life) are vitally important as these parameters are used to… (more)

Subjects/Keywords: Pharmaceutical sciences; Cellular biology; Pharmacology; Cationic Amphiphilic Drugs; Drug distribution; Drug Drug interaction; intracellular distribution; Lysosome; Lysosomotropic

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APA (6th Edition):

Logan, R. (2013). Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21626

Chicago Manual of Style (16th Edition):

Logan, Randall. “Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function.” 2013. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21626.

MLA Handbook (7th Edition):

Logan, Randall. “Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function.” 2013. Web. 28 Sep 2020.

Vancouver:

Logan R. Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21626.

Council of Science Editors:

Logan R. Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/21626


University of Kansas

24. Badawi, Yomna Hassan. The roles of Hypoxia Inducible Factor-1, Glutamate and their interaction in Ischemic Tolerance.

Degree: PhD, Neurosciences, 2014, University of Kansas

 Stroke is a debilitating disorder with no effective treatments. The clinical importance of promoting cerebral ischemic tolerance is apparent; however, our knowledge of the signaling… (more)

Subjects/Keywords: Neurosciences; Pharmacology; Toxicology; Astrocytes; Glutamate; HIF-1; Neurons; Reactive Oxygen Species; Stroke

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APA (6th Edition):

Badawi, Y. H. (2014). The roles of Hypoxia Inducible Factor-1, Glutamate and their interaction in Ischemic Tolerance. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21632

Chicago Manual of Style (16th Edition):

Badawi, Yomna Hassan. “The roles of Hypoxia Inducible Factor-1, Glutamate and their interaction in Ischemic Tolerance.” 2014. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/21632.

MLA Handbook (7th Edition):

Badawi, Yomna Hassan. “The roles of Hypoxia Inducible Factor-1, Glutamate and their interaction in Ischemic Tolerance.” 2014. Web. 28 Sep 2020.

Vancouver:

Badawi YH. The roles of Hypoxia Inducible Factor-1, Glutamate and their interaction in Ischemic Tolerance. [Internet] [Doctoral dissertation]. University of Kansas; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/21632.

Council of Science Editors:

Badawi YH. The roles of Hypoxia Inducible Factor-1, Glutamate and their interaction in Ischemic Tolerance. [Doctoral Dissertation]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21632


University of Kansas

25. Creamer, Jessica Stephens. The Development of Capillary and Microchip Electrophoresis Methods for the Analysis of Pharmaceuticals in Developing Countries.

Degree: PhD, Pharmaceutical Chemistry, 2014, University of Kansas

 Maintaining a consistent supply of pharmaceuticals to developing countries could save millions of lives per year. One of the major roadblocks in this effort is… (more)

Subjects/Keywords: Analytical chemistry; Biotechnology; Capillary electrophoresis; Developing countries; Microchip electrophoresis; Pharmaceutical analysis; Protein therapeutic

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APA (6th Edition):

Creamer, J. S. (2014). The Development of Capillary and Microchip Electrophoresis Methods for the Analysis of Pharmaceuticals in Developing Countries. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/22513

Chicago Manual of Style (16th Edition):

Creamer, Jessica Stephens. “The Development of Capillary and Microchip Electrophoresis Methods for the Analysis of Pharmaceuticals in Developing Countries.” 2014. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/22513.

MLA Handbook (7th Edition):

Creamer, Jessica Stephens. “The Development of Capillary and Microchip Electrophoresis Methods for the Analysis of Pharmaceuticals in Developing Countries.” 2014. Web. 28 Sep 2020.

Vancouver:

Creamer JS. The Development of Capillary and Microchip Electrophoresis Methods for the Analysis of Pharmaceuticals in Developing Countries. [Internet] [Doctoral dissertation]. University of Kansas; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/22513.

Council of Science Editors:

Creamer JS. The Development of Capillary and Microchip Electrophoresis Methods for the Analysis of Pharmaceuticals in Developing Countries. [Doctoral Dissertation]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/22513


University of Kansas

26. Hu, Yue. Characterization, Stabilization and Formulation Design of IgG and Secretory IgA Monoclonal Antibody Candidates during Storage and Administration.

Degree: PhD, Pharmaceutical Chemistry, 2019, University of Kansas

 ABSTRACT Monoclonal antibodies (mAbs) have become a class of therapeutic protein-based drugs of high importance for treating numerous human diseases. As a complex, delicate three… (more)

Subjects/Keywords: Pharmaceutical sciences

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APA (6th Edition):

Hu, Y. (2019). Characterization, Stabilization and Formulation Design of IgG and Secretory IgA Monoclonal Antibody Candidates during Storage and Administration. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/29546

Chicago Manual of Style (16th Edition):

Hu, Yue. “Characterization, Stabilization and Formulation Design of IgG and Secretory IgA Monoclonal Antibody Candidates during Storage and Administration.” 2019. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/29546.

MLA Handbook (7th Edition):

Hu, Yue. “Characterization, Stabilization and Formulation Design of IgG and Secretory IgA Monoclonal Antibody Candidates during Storage and Administration.” 2019. Web. 28 Sep 2020.

Vancouver:

Hu Y. Characterization, Stabilization and Formulation Design of IgG and Secretory IgA Monoclonal Antibody Candidates during Storage and Administration. [Internet] [Doctoral dissertation]. University of Kansas; 2019. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/29546.

Council of Science Editors:

Hu Y. Characterization, Stabilization and Formulation Design of IgG and Secretory IgA Monoclonal Antibody Candidates during Storage and Administration. [Doctoral Dissertation]. University of Kansas; 2019. Available from: http://hdl.handle.net/1808/29546


University of Kansas

27. Agarwal, Sanjeev. Analytical characterization and formulation development of a trivalent subunit rotavirus vaccine for the developing world.

Degree: PhD, Pharmaceutical Chemistry, 2019, University of Kansas

 Although live attenuated, orally delivered rotavirus (RV) vaccines are available globally to provide protection against enteric RV disease, efficacy is substantially lower in low to… (more)

Subjects/Keywords: Pharmaceutical sciences; Adjuvant; Formulation; Preservative; Rotavirus; Stability; Vaccine

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APA (6th Edition):

Agarwal, S. (2019). Analytical characterization and formulation development of a trivalent subunit rotavirus vaccine for the developing world. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/29840

Chicago Manual of Style (16th Edition):

Agarwal, Sanjeev. “Analytical characterization and formulation development of a trivalent subunit rotavirus vaccine for the developing world.” 2019. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/29840.

MLA Handbook (7th Edition):

Agarwal, Sanjeev. “Analytical characterization and formulation development of a trivalent subunit rotavirus vaccine for the developing world.” 2019. Web. 28 Sep 2020.

Vancouver:

Agarwal S. Analytical characterization and formulation development of a trivalent subunit rotavirus vaccine for the developing world. [Internet] [Doctoral dissertation]. University of Kansas; 2019. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/29840.

Council of Science Editors:

Agarwal S. Analytical characterization and formulation development of a trivalent subunit rotavirus vaccine for the developing world. [Doctoral Dissertation]. University of Kansas; 2019. Available from: http://hdl.handle.net/1808/29840


University of Kansas

28. Kang, Huan. Physicochemical stability and effector function of IgG4-Fc: impact of photo-induced chemical modification and glycosylation.

Degree: PhD, Pharmaceutical Chemistry, 2019, University of Kansas

 Immunoglobulin gamma monoclonal antibodies are glycoproteins that have emerged as powerful and promising protein therapeutics. During the process of production, storage and transportation, exposure to… (more)

Subjects/Keywords: Pharmaceutical sciences

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APA (6th Edition):

Kang, H. (2019). Physicochemical stability and effector function of IgG4-Fc: impact of photo-induced chemical modification and glycosylation. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/30213

Chicago Manual of Style (16th Edition):

Kang, Huan. “Physicochemical stability and effector function of IgG4-Fc: impact of photo-induced chemical modification and glycosylation.” 2019. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/30213.

MLA Handbook (7th Edition):

Kang, Huan. “Physicochemical stability and effector function of IgG4-Fc: impact of photo-induced chemical modification and glycosylation.” 2019. Web. 28 Sep 2020.

Vancouver:

Kang H. Physicochemical stability and effector function of IgG4-Fc: impact of photo-induced chemical modification and glycosylation. [Internet] [Doctoral dissertation]. University of Kansas; 2019. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/30213.

Council of Science Editors:

Kang H. Physicochemical stability and effector function of IgG4-Fc: impact of photo-induced chemical modification and glycosylation. [Doctoral Dissertation]. University of Kansas; 2019. Available from: http://hdl.handle.net/1808/30213


University of Kansas

29. Arora, Jayant. Towards a greater mechanistic understanding of reversible protein-protein interactions and irreversible aggregation of IgG1 monoclonal antibodies.

Degree: PhD, Pharmaceutical Chemistry, 2016, University of Kansas

 Immunoglobulin G1 monoclonal antibodies (IgG1-mAbs) are one of the most important and fastest growing class of biotherapeutic agents. These mAbs are being used to treat… (more)

Subjects/Keywords: Pharmaceutical sciences; High protein concentration; Hydrogen exchange mass spectrometry; Monoclonal antibodies; Protein aggregation; Protein-protein interactions; Reversible self-association

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APA (6th Edition):

Arora, J. (2016). Towards a greater mechanistic understanding of reversible protein-protein interactions and irreversible aggregation of IgG1 monoclonal antibodies. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/25363

Chicago Manual of Style (16th Edition):

Arora, Jayant. “Towards a greater mechanistic understanding of reversible protein-protein interactions and irreversible aggregation of IgG1 monoclonal antibodies.” 2016. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/25363.

MLA Handbook (7th Edition):

Arora, Jayant. “Towards a greater mechanistic understanding of reversible protein-protein interactions and irreversible aggregation of IgG1 monoclonal antibodies.” 2016. Web. 28 Sep 2020.

Vancouver:

Arora J. Towards a greater mechanistic understanding of reversible protein-protein interactions and irreversible aggregation of IgG1 monoclonal antibodies. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/25363.

Council of Science Editors:

Arora J. Towards a greater mechanistic understanding of reversible protein-protein interactions and irreversible aggregation of IgG1 monoclonal antibodies. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/25363


University of Kansas

30. Al-Hossaini, Abdullah. Analytical Methods for the Study of Opioid Peptides.

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

 Dynorphin A 1-17 [Tyr-Gly-Gly-Phe-Leu-Arg-Arg-Ile-Arg-Pro-Lys-Leu-Lys-Trp-Asp-Asn-Gln] is an endogenous opioid peptide. It is widely distributed in blood and CNS tissue and exhibits a high affinity to the… (more)

Subjects/Keywords: Pharmaceutical sciences; Capillary Electrophoresis; Dynorphin A; Gold nanoparticles; Microchip electrophoresis

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APA (6th Edition):

Al-Hossaini, A. (2017). Analytical Methods for the Study of Opioid Peptides. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27338

Chicago Manual of Style (16th Edition):

Al-Hossaini, Abdullah. “Analytical Methods for the Study of Opioid Peptides.” 2017. Doctoral Dissertation, University of Kansas. Accessed September 28, 2020. http://hdl.handle.net/1808/27338.

MLA Handbook (7th Edition):

Al-Hossaini, Abdullah. “Analytical Methods for the Study of Opioid Peptides.” 2017. Web. 28 Sep 2020.

Vancouver:

Al-Hossaini A. Analytical Methods for the Study of Opioid Peptides. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/1808/27338.

Council of Science Editors:

Al-Hossaini A. Analytical Methods for the Study of Opioid Peptides. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/27338

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