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You searched for subject:(PEGylation). Showing records 1 – 30 of 64 total matches.

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University of Waikato

1. Kapadi, Ajith Nayak. Size Exclusion PEGylation Reaction Chromatography Modelling .

Degree: 2006, University of Waikato

 Size exclusion PEGylation reaction chromatography was investigated using a model developed by Fee (2005). Column dispersion was neglected and the PEGylation reaction was modelled as… (more)

Subjects/Keywords: PEGylation

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APA (6th Edition):

Kapadi, A. N. (2006). Size Exclusion PEGylation Reaction Chromatography Modelling . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/2504

Chicago Manual of Style (16th Edition):

Kapadi, Ajith Nayak. “Size Exclusion PEGylation Reaction Chromatography Modelling .” 2006. Masters Thesis, University of Waikato. Accessed October 30, 2020. http://hdl.handle.net/10289/2504.

MLA Handbook (7th Edition):

Kapadi, Ajith Nayak. “Size Exclusion PEGylation Reaction Chromatography Modelling .” 2006. Web. 30 Oct 2020.

Vancouver:

Kapadi AN. Size Exclusion PEGylation Reaction Chromatography Modelling . [Internet] [Masters thesis]. University of Waikato; 2006. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10289/2504.

Council of Science Editors:

Kapadi AN. Size Exclusion PEGylation Reaction Chromatography Modelling . [Masters Thesis]. University of Waikato; 2006. Available from: http://hdl.handle.net/10289/2504


University of the Western Cape

2. Fipaza, Vincent Lukhanyiso. The development of functionalized metallic nanoparticles for the treatment of brain cancer .

Degree: 2019, University of the Western Cape

 Cancers of the nervous system often result from abnormal and uncontrolled growth of cells in nervous tissue. Glioblastoma Multiforme (GBM) and neuroblastoma (NB) are among… (more)

Subjects/Keywords: Nanoparticles; PEGylation; Cancer; Treatment; Cytotoxicity

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APA (6th Edition):

Fipaza, V. L. (2019). The development of functionalized metallic nanoparticles for the treatment of brain cancer . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/7140

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):

Fipaza, Vincent Lukhanyiso. “The development of functionalized metallic nanoparticles for the treatment of brain cancer .” 2019. Thesis, University of the Western Cape. Accessed October 30, 2020. http://hdl.handle.net/11394/7140.

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

MLA Handbook (7th Edition):

Fipaza, Vincent Lukhanyiso. “The development of functionalized metallic nanoparticles for the treatment of brain cancer .” 2019. Web. 30 Oct 2020.

Vancouver:

Fipaza VL. The development of functionalized metallic nanoparticles for the treatment of brain cancer . [Internet] [Thesis]. University of the Western Cape; 2019. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11394/7140.

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

Council of Science Editors:

Fipaza VL. The development of functionalized metallic nanoparticles for the treatment of brain cancer . [Thesis]. University of the Western Cape; 2019. Available from: http://hdl.handle.net/11394/7140

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


University of Michigan

3. Onyskiw, Jr., Peter John. Particle-Blood Dynamics: Adhesion of Vascular-Targeted Pegylated Particles and Blood Cells in Flow.

Degree: PhD, Chemical Engineering, 2015, University of Michigan

 Vascular targeting is a viable strategy for the therapeutic intervention of inflammatory diseases such as cardiovascular disease. The multiple components of blood (red blood cell,… (more)

Subjects/Keywords: Vascular Targeted; PEGylation; Chemical Engineering; Engineering

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APA (6th Edition):

Onyskiw, Jr., P. J. (2015). Particle-Blood Dynamics: Adhesion of Vascular-Targeted Pegylated Particles and Blood Cells in Flow. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111454

Chicago Manual of Style (16th Edition):

Onyskiw, Jr., Peter John. “Particle-Blood Dynamics: Adhesion of Vascular-Targeted Pegylated Particles and Blood Cells in Flow.” 2015. Doctoral Dissertation, University of Michigan. Accessed October 30, 2020. http://hdl.handle.net/2027.42/111454.

MLA Handbook (7th Edition):

Onyskiw, Jr., Peter John. “Particle-Blood Dynamics: Adhesion of Vascular-Targeted Pegylated Particles and Blood Cells in Flow.” 2015. Web. 30 Oct 2020.

Vancouver:

Onyskiw, Jr. PJ. Particle-Blood Dynamics: Adhesion of Vascular-Targeted Pegylated Particles and Blood Cells in Flow. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2027.42/111454.

Council of Science Editors:

Onyskiw, Jr. PJ. Particle-Blood Dynamics: Adhesion of Vascular-Targeted Pegylated Particles and Blood Cells in Flow. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111454


Université Paris-Sud – Paris XI

4. Bui, Duc Trung. Adressage de Nanomédicaments à base de squalène : Targeted squalene-based nanomedicines.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2013, Université Paris-Sud – Paris XI

Les nanoparticules de Gemcitabine-Squalène (Gem-Sq), synthétisées suivant le concept de « squalénisation », ont montré des activités anticancéreuses très supérieures à celles obtenues en présence… (more)

Subjects/Keywords: Gemcitabine; Squalène; Squalénisation; Nanoparticules; Ciblage; PEGylation; Polyisoprène; Cancer; Gemcitabine; Squalene; Squalenoylation; Nanoparticles; Targeting; PEGylation; Polyisoprene; Cancer

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APA (6th Edition):

Bui, D. T. (2013). Adressage de Nanomédicaments à base de squalène : Targeted squalene-based nanomedicines. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA114848

Chicago Manual of Style (16th Edition):

Bui, Duc Trung. “Adressage de Nanomédicaments à base de squalène : Targeted squalene-based nanomedicines.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 30, 2020. http://www.theses.fr/2013PA114848.

MLA Handbook (7th Edition):

Bui, Duc Trung. “Adressage de Nanomédicaments à base de squalène : Targeted squalene-based nanomedicines.” 2013. Web. 30 Oct 2020.

Vancouver:

Bui DT. Adressage de Nanomédicaments à base de squalène : Targeted squalene-based nanomedicines. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Oct 30]. Available from: http://www.theses.fr/2013PA114848.

Council of Science Editors:

Bui DT. Adressage de Nanomédicaments à base de squalène : Targeted squalene-based nanomedicines. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA114848


Carnegie Mellon University

5. Weinberg, Justin B. Competitive IgG Adsorption on Protein A Chromatography Resins and Improving Resin Performance with PEGylated Ligands.

Degree: 2017, Carnegie Mellon University

 Protein A (ProA) chromatography is a bioseparations technique employed throughout the biopharmaceutical industry for the selective capture and purification of IgG-class monoclonal antibodies (mAbs) and… (more)

Subjects/Keywords: adsorption; bioprocessing; chromatography; monoclonal antibodies; PEGylation; Protein A

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APA (6th Edition):

Weinberg, J. B. (2017). Competitive IgG Adsorption on Protein A Chromatography Resins and Improving Resin Performance with PEGylated Ligands. (Thesis). Carnegie Mellon University. Retrieved from http://repository.cmu.edu/dissertations/1075

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):

Weinberg, Justin B. “Competitive IgG Adsorption on Protein A Chromatography Resins and Improving Resin Performance with PEGylated Ligands.” 2017. Thesis, Carnegie Mellon University. Accessed October 30, 2020. http://repository.cmu.edu/dissertations/1075.

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

MLA Handbook (7th Edition):

Weinberg, Justin B. “Competitive IgG Adsorption on Protein A Chromatography Resins and Improving Resin Performance with PEGylated Ligands.” 2017. Web. 30 Oct 2020.

Vancouver:

Weinberg JB. Competitive IgG Adsorption on Protein A Chromatography Resins and Improving Resin Performance with PEGylated Ligands. [Internet] [Thesis]. Carnegie Mellon University; 2017. [cited 2020 Oct 30]. Available from: http://repository.cmu.edu/dissertations/1075.

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

Council of Science Editors:

Weinberg JB. Competitive IgG Adsorption on Protein A Chromatography Resins and Improving Resin Performance with PEGylated Ligands. [Thesis]. Carnegie Mellon University; 2017. Available from: http://repository.cmu.edu/dissertations/1075

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


UCLA

6. Park, Juyoung. Systemic Delivery of PEGylated NEL-like Molecule-1 (NELL-1) as A Novel Strategy for Osteoinductive Therapy.

Degree: Oral Biology, 2014, UCLA

 NELL-1 is an osteogenic, secretory molecule previously shown to enhance bone regeneration in multiple rodent and ovine orthopedic defect models. Excitingly, we have recently shown… (more)

Subjects/Keywords: Dentistry; biological half-life; NELL-1; osteoporosis; PEGylation; systemic osteogenic therapy

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APA (6th Edition):

Park, J. (2014). Systemic Delivery of PEGylated NEL-like Molecule-1 (NELL-1) as A Novel Strategy for Osteoinductive Therapy. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1929n9gg

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):

Park, Juyoung. “Systemic Delivery of PEGylated NEL-like Molecule-1 (NELL-1) as A Novel Strategy for Osteoinductive Therapy.” 2014. Thesis, UCLA. Accessed October 30, 2020. http://www.escholarship.org/uc/item/1929n9gg.

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

MLA Handbook (7th Edition):

Park, Juyoung. “Systemic Delivery of PEGylated NEL-like Molecule-1 (NELL-1) as A Novel Strategy for Osteoinductive Therapy.” 2014. Web. 30 Oct 2020.

Vancouver:

Park J. Systemic Delivery of PEGylated NEL-like Molecule-1 (NELL-1) as A Novel Strategy for Osteoinductive Therapy. [Internet] [Thesis]. UCLA; 2014. [cited 2020 Oct 30]. Available from: http://www.escholarship.org/uc/item/1929n9gg.

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

Council of Science Editors:

Park J. Systemic Delivery of PEGylated NEL-like Molecule-1 (NELL-1) as A Novel Strategy for Osteoinductive Therapy. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/1929n9gg

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


University of Alberta

7. Bhandari, Krishna H. Bone Targeting Salmon Calcitonin Analogues as Drug Delivery Systems for Bone Disease.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2012, University of Alberta

 The objective of this thesis was to design bone targeting salmon calcitonin (sCT) analogues as drug delivery systems for bone diseases. Non-PEGylated salmon calcitonin-bisphosphonate (sCT-BP)… (more)

Subjects/Keywords: Bone Targeting; Salmon Calcitonin PEGylation,; Osteoporosis and Arthritis

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APA (6th Edition):

Bhandari, K. H. (2012). Bone Targeting Salmon Calcitonin Analogues as Drug Delivery Systems for Bone Disease. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/9w032407m

Chicago Manual of Style (16th Edition):

Bhandari, Krishna H. “Bone Targeting Salmon Calcitonin Analogues as Drug Delivery Systems for Bone Disease.” 2012. Doctoral Dissertation, University of Alberta. Accessed October 30, 2020. https://era.library.ualberta.ca/files/9w032407m.

MLA Handbook (7th Edition):

Bhandari, Krishna H. “Bone Targeting Salmon Calcitonin Analogues as Drug Delivery Systems for Bone Disease.” 2012. Web. 30 Oct 2020.

Vancouver:

Bhandari KH. Bone Targeting Salmon Calcitonin Analogues as Drug Delivery Systems for Bone Disease. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Oct 30]. Available from: https://era.library.ualberta.ca/files/9w032407m.

Council of Science Editors:

Bhandari KH. Bone Targeting Salmon Calcitonin Analogues as Drug Delivery Systems for Bone Disease. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/9w032407m


Cornell University

8. Cong, Ying. Silica-Based Nanoparticles For Cancer Theranostics: Drug Loading Mechanism Of mC Dots And Conductivity Study Of C’ Dots Synthesis Kinetics And PEGylation Process.

Degree: M.S., Materials Science and Engineering, Materials Science and Engineering, 2015, Cornell University

Subjects/Keywords: silica nanoparticles; PEGylation; drug delivery

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APA (6th Edition):

Cong, Y. (2015). Silica-Based Nanoparticles For Cancer Theranostics: Drug Loading Mechanism Of mC Dots And Conductivity Study Of C’ Dots Synthesis Kinetics And PEGylation Process. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/41174

Chicago Manual of Style (16th Edition):

Cong, Ying. “Silica-Based Nanoparticles For Cancer Theranostics: Drug Loading Mechanism Of mC Dots And Conductivity Study Of C’ Dots Synthesis Kinetics And PEGylation Process.” 2015. Masters Thesis, Cornell University. Accessed October 30, 2020. http://hdl.handle.net/1813/41174.

MLA Handbook (7th Edition):

Cong, Ying. “Silica-Based Nanoparticles For Cancer Theranostics: Drug Loading Mechanism Of mC Dots And Conductivity Study Of C’ Dots Synthesis Kinetics And PEGylation Process.” 2015. Web. 30 Oct 2020.

Vancouver:

Cong Y. Silica-Based Nanoparticles For Cancer Theranostics: Drug Loading Mechanism Of mC Dots And Conductivity Study Of C’ Dots Synthesis Kinetics And PEGylation Process. [Internet] [Masters thesis]. Cornell University; 2015. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1813/41174.

Council of Science Editors:

Cong Y. Silica-Based Nanoparticles For Cancer Theranostics: Drug Loading Mechanism Of mC Dots And Conductivity Study Of C’ Dots Synthesis Kinetics And PEGylation Process. [Masters Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41174


Texas A&M University

9. Ritter, Dustin W. Development and Characterization of Stable Glycoenzyme Conjugates.

Degree: PhD, Biomedical Engineering, 2014, Texas A&M University

 Optical glucose biosensors are being developed for long-term monitoring in diabetic individuals. These sensors rely upon the enzyme glucose oxidase, and loss of enzymatic activity… (more)

Subjects/Keywords: enzyme stabilization; optical biosensor; glucose oxidase; catalase; PEGylation; crosslinking

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APA (6th Edition):

Ritter, D. W. (2014). Development and Characterization of Stable Glycoenzyme Conjugates. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154017

Chicago Manual of Style (16th Edition):

Ritter, Dustin W. “Development and Characterization of Stable Glycoenzyme Conjugates.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 30, 2020. http://hdl.handle.net/1969.1/154017.

MLA Handbook (7th Edition):

Ritter, Dustin W. “Development and Characterization of Stable Glycoenzyme Conjugates.” 2014. Web. 30 Oct 2020.

Vancouver:

Ritter DW. Development and Characterization of Stable Glycoenzyme Conjugates. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1969.1/154017.

Council of Science Editors:

Ritter DW. Development and Characterization of Stable Glycoenzyme Conjugates. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154017


McMaster University

10. McNelles, Stuart Alexander. Dendrimers for Imaging and Molecular Sieving.

Degree: PhD, 2019, McMaster University

The Enhanced Permeability and Retention (EPR) effect has seen considerable exploration by many researchers since it’s discovery by Maeda et al in 1985. Polymers and… (more)

Subjects/Keywords: Polymer Chemistry; Dendrimers; Bis-MPA; Nuclear Imaging; PEGylation; Polymer-Protein Conjugates

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APA (6th Edition):

McNelles, S. A. (2019). Dendrimers for Imaging and Molecular Sieving. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/24745

Chicago Manual of Style (16th Edition):

McNelles, Stuart Alexander. “Dendrimers for Imaging and Molecular Sieving.” 2019. Doctoral Dissertation, McMaster University. Accessed October 30, 2020. http://hdl.handle.net/11375/24745.

MLA Handbook (7th Edition):

McNelles, Stuart Alexander. “Dendrimers for Imaging and Molecular Sieving.” 2019. Web. 30 Oct 2020.

Vancouver:

McNelles SA. Dendrimers for Imaging and Molecular Sieving. [Internet] [Doctoral dissertation]. McMaster University; 2019. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11375/24745.

Council of Science Editors:

McNelles SA. Dendrimers for Imaging and Molecular Sieving. [Doctoral Dissertation]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/24745


University of KwaZulu-Natal

11. Daniels, Aliscia Nicole. Functionalised gold nanpparticle delivry for cMYC siRNA in cancer gene theraphy.

Degree: 2018, University of KwaZulu-Natal

 RNA interference (RNAi), which can be induced by chemically synthesized small interfering RNA (siRNA), has emerged as a powerful tool in molecular biology for the… (more)

Subjects/Keywords: Gold nanoparticles.; PEGylation.; Gene silencing.; Cytotoxicity.; Cancer gene theraphy.

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APA (6th Edition):

Daniels, A. N. (2018). Functionalised gold nanpparticle delivry for cMYC siRNA in cancer gene theraphy. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/17542

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):

Daniels, Aliscia Nicole. “Functionalised gold nanpparticle delivry for cMYC siRNA in cancer gene theraphy.” 2018. Thesis, University of KwaZulu-Natal. Accessed October 30, 2020. https://researchspace.ukzn.ac.za/handle/10413/17542.

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

MLA Handbook (7th Edition):

Daniels, Aliscia Nicole. “Functionalised gold nanpparticle delivry for cMYC siRNA in cancer gene theraphy.” 2018. Web. 30 Oct 2020.

Vancouver:

Daniels AN. Functionalised gold nanpparticle delivry for cMYC siRNA in cancer gene theraphy. [Internet] [Thesis]. University of KwaZulu-Natal; 2018. [cited 2020 Oct 30]. Available from: https://researchspace.ukzn.ac.za/handle/10413/17542.

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

Council of Science Editors:

Daniels AN. Functionalised gold nanpparticle delivry for cMYC siRNA in cancer gene theraphy. [Thesis]. University of KwaZulu-Natal; 2018. Available from: https://researchspace.ukzn.ac.za/handle/10413/17542

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


University of Lund

12. Garting, Tommy. Microrheology of Concentrated Protein Solutions.

Degree: 2019, University of Lund

 The behavior of concentrated protein solutions is of general high interest due to implications in, for example, biological systems and medical applications. It is necessary… (more)

Subjects/Keywords: Physical Chemistry; Microrheology; Dynamic Light Scattering; Protein; Pegylation; Viscosity

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APA (6th Edition):

Garting, T. (2019). Microrheology of Concentrated Protein Solutions. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/4b222388-a7b6-42de-b195-4e3b653be572 ; https://portal.research.lu.se/ws/files/57318273/Garting_Kappa.pdf

Chicago Manual of Style (16th Edition):

Garting, Tommy. “Microrheology of Concentrated Protein Solutions.” 2019. Doctoral Dissertation, University of Lund. Accessed October 30, 2020. https://lup.lub.lu.se/record/4b222388-a7b6-42de-b195-4e3b653be572 ; https://portal.research.lu.se/ws/files/57318273/Garting_Kappa.pdf.

MLA Handbook (7th Edition):

Garting, Tommy. “Microrheology of Concentrated Protein Solutions.” 2019. Web. 30 Oct 2020.

Vancouver:

Garting T. Microrheology of Concentrated Protein Solutions. [Internet] [Doctoral dissertation]. University of Lund; 2019. [cited 2020 Oct 30]. Available from: https://lup.lub.lu.se/record/4b222388-a7b6-42de-b195-4e3b653be572 ; https://portal.research.lu.se/ws/files/57318273/Garting_Kappa.pdf.

Council of Science Editors:

Garting T. Microrheology of Concentrated Protein Solutions. [Doctoral Dissertation]. University of Lund; 2019. Available from: https://lup.lub.lu.se/record/4b222388-a7b6-42de-b195-4e3b653be572 ; https://portal.research.lu.se/ws/files/57318273/Garting_Kappa.pdf


Brigham Young University

13. Lawrence, Paul B. Criteria for Selecting PEGylation Sites on Proteins for Higher Thermodynamic Stability.

Degree: PhD, 2016, Brigham Young University

PEGylation of protein side-chains has been used for more than 30 years to enhance the pharmacokinetic properties of protein drugs, and has been enabled by… (more)

Subjects/Keywords: PEGylation; Therapeutic Proteins; Thermodynamic Stability; Circular Dichroism; beta-sheet; Chemistry

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APA (6th Edition):

Lawrence, P. B. (2016). Criteria for Selecting PEGylation Sites on Proteins for Higher Thermodynamic Stability. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7259&context=etd

Chicago Manual of Style (16th Edition):

Lawrence, Paul B. “Criteria for Selecting PEGylation Sites on Proteins for Higher Thermodynamic Stability.” 2016. Doctoral Dissertation, Brigham Young University. Accessed October 30, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7259&context=etd.

MLA Handbook (7th Edition):

Lawrence, Paul B. “Criteria for Selecting PEGylation Sites on Proteins for Higher Thermodynamic Stability.” 2016. Web. 30 Oct 2020.

Vancouver:

Lawrence PB. Criteria for Selecting PEGylation Sites on Proteins for Higher Thermodynamic Stability. [Internet] [Doctoral dissertation]. Brigham Young University; 2016. [cited 2020 Oct 30]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7259&context=etd.

Council of Science Editors:

Lawrence PB. Criteria for Selecting PEGylation Sites on Proteins for Higher Thermodynamic Stability. [Doctoral Dissertation]. Brigham Young University; 2016. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7259&context=etd


Georgia State University

14. Patel, Anvi N. Development of New Series of Protein Based MRI Contrast Agents: ProCA1 Variants and Humanized ProCA32.

Degree: MS, Chemistry, 2015, Georgia State University

  MRI is a noninvasive technique used for disease diagnosis. However, recent clinically used MRI contrast agents exhibit low relaxivity, high metal toxicity due to… (more)

Subjects/Keywords: Magnetic Resonance Imaging; Contrast agents; Gadolinium; Relaxivity; Metal binding; PEGylation

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APA (6th Edition):

Patel, A. N. (2015). Development of New Series of Protein Based MRI Contrast Agents: ProCA1 Variants and Humanized ProCA32. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/69

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):

Patel, Anvi N. “Development of New Series of Protein Based MRI Contrast Agents: ProCA1 Variants and Humanized ProCA32.” 2015. Thesis, Georgia State University. Accessed October 30, 2020. https://scholarworks.gsu.edu/chemistry_theses/69.

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

MLA Handbook (7th Edition):

Patel, Anvi N. “Development of New Series of Protein Based MRI Contrast Agents: ProCA1 Variants and Humanized ProCA32.” 2015. Web. 30 Oct 2020.

Vancouver:

Patel AN. Development of New Series of Protein Based MRI Contrast Agents: ProCA1 Variants and Humanized ProCA32. [Internet] [Thesis]. Georgia State University; 2015. [cited 2020 Oct 30]. Available from: https://scholarworks.gsu.edu/chemistry_theses/69.

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

Council of Science Editors:

Patel AN. Development of New Series of Protein Based MRI Contrast Agents: ProCA1 Variants and Humanized ProCA32. [Thesis]. Georgia State University; 2015. Available from: https://scholarworks.gsu.edu/chemistry_theses/69

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

15. Prado, Sally Müller Affonso. Aplicabilidade do antígeno tetânico conjugado com derivados do Monometoxi-polietilenoglicol.

Degree: PhD, Biotecnologia, 2008, University of São Paulo

O Monometoxi-polietilenoglicol succinimidil ácido propiônico (mPEG-SPA 5 e 20 kDa) foi analisado como adjuvante e inibidor da atividade neurotóxica da toxina tetânica (TxT) adsorvida ou… (more)

Subjects/Keywords: Adjuvantes imunológicos; Antígenos; Antigens; Immunologics adjuvants; mPEG; mPEG; PEG; PEG; Peglação; Pegylation; Toxinas; Toxins

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APA (6th Edition):

Prado, S. M. A. (2008). Aplicabilidade do antígeno tetânico conjugado com derivados do Monometoxi-polietilenoglicol. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09032009-151619/ ;

Chicago Manual of Style (16th Edition):

Prado, Sally Müller Affonso. “Aplicabilidade do antígeno tetânico conjugado com derivados do Monometoxi-polietilenoglicol.” 2008. Doctoral Dissertation, University of São Paulo. Accessed October 30, 2020. http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09032009-151619/ ;.

MLA Handbook (7th Edition):

Prado, Sally Müller Affonso. “Aplicabilidade do antígeno tetânico conjugado com derivados do Monometoxi-polietilenoglicol.” 2008. Web. 30 Oct 2020.

Vancouver:

Prado SMA. Aplicabilidade do antígeno tetânico conjugado com derivados do Monometoxi-polietilenoglicol. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2020 Oct 30]. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09032009-151619/ ;.

Council of Science Editors:

Prado SMA. Aplicabilidade do antígeno tetânico conjugado com derivados do Monometoxi-polietilenoglicol. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/87/87131/tde-09032009-151619/ ;


NSYSU

16. Tseng, Po-Jung. (1)Newly Designed Cycloplatinated Polymer Dots as Photocatalysts for Visible Lightâdriven Hydrogen Evolution(2)Modification Polymer Dots with PEG Moieties to Reduce Non-specific Biomolecular Adsorption.

Degree: Master, Chemistry, 2018, NSYSU

 (1) Newly Designed Cycloplatinated Polymer Dots as Photocatalysts for Visible Lightâdriven Hydrogen Evolution Overuse of fossil fuels is intensifying air pollution and greenhouse effect. Thus,… (more)

Subjects/Keywords: Photocatalysts; Hydrogen evolution; Visible light; PEGylation; Non-specific effect; Polymer dots; Bioimaging; FRET; Semiconducting polymers

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APA (6th Edition):

Tseng, P. (2018). (1)Newly Designed Cycloplatinated Polymer Dots as Photocatalysts for Visible Lightâdriven Hydrogen Evolution(2)Modification Polymer Dots with PEG Moieties to Reduce Non-specific Biomolecular Adsorption. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0625118-234027

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):

Tseng, Po-Jung. “(1)Newly Designed Cycloplatinated Polymer Dots as Photocatalysts for Visible Lightâdriven Hydrogen Evolution(2)Modification Polymer Dots with PEG Moieties to Reduce Non-specific Biomolecular Adsorption.” 2018. Thesis, NSYSU. Accessed October 30, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0625118-234027.

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

MLA Handbook (7th Edition):

Tseng, Po-Jung. “(1)Newly Designed Cycloplatinated Polymer Dots as Photocatalysts for Visible Lightâdriven Hydrogen Evolution(2)Modification Polymer Dots with PEG Moieties to Reduce Non-specific Biomolecular Adsorption.” 2018. Web. 30 Oct 2020.

Vancouver:

Tseng P. (1)Newly Designed Cycloplatinated Polymer Dots as Photocatalysts for Visible Lightâdriven Hydrogen Evolution(2)Modification Polymer Dots with PEG Moieties to Reduce Non-specific Biomolecular Adsorption. [Internet] [Thesis]. NSYSU; 2018. [cited 2020 Oct 30]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0625118-234027.

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

Council of Science Editors:

Tseng P. (1)Newly Designed Cycloplatinated Polymer Dots as Photocatalysts for Visible Lightâdriven Hydrogen Evolution(2)Modification Polymer Dots with PEG Moieties to Reduce Non-specific Biomolecular Adsorption. [Thesis]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0625118-234027

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

17. CRUZ, RICARDO MACHADO. New solid forms of itraconazole and their pharmaceutical applications.

Degree: School of Pharmacy & Pharma. Sciences. Discipline of Pharmacy, 2020, Trinity College Dublin

 Itraconazole (ITR) is an active pharmaceutical ingredient (API) with a broad-spectrum antifungal activity. This API has a very low solubility, which can hinder its bioavailability… (more)

Subjects/Keywords: Itraconazole; Cocrystals; Nanoparticles; Mucoadhesivity; Liquid Crystal; Nanococrystal; Pulmonary Delivery; Terephthalic Acid; PEGylation; Poly(ethylene glycol)

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APA (6th Edition):

CRUZ, R. M. (2020). New solid forms of itraconazole and their pharmaceutical applications. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/92698

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):

CRUZ, RICARDO MACHADO. “New solid forms of itraconazole and their pharmaceutical applications.” 2020. Thesis, Trinity College Dublin. Accessed October 30, 2020. http://hdl.handle.net/2262/92698.

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

MLA Handbook (7th Edition):

CRUZ, RICARDO MACHADO. “New solid forms of itraconazole and their pharmaceutical applications.” 2020. Web. 30 Oct 2020.

Vancouver:

CRUZ RM. New solid forms of itraconazole and their pharmaceutical applications. [Internet] [Thesis]. Trinity College Dublin; 2020. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2262/92698.

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

Council of Science Editors:

CRUZ RM. New solid forms of itraconazole and their pharmaceutical applications. [Thesis]. Trinity College Dublin; 2020. Available from: http://hdl.handle.net/2262/92698

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


Université Catholique de Louvain

18. Guichard, Marie-Julie. Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease.

Degree: 2018, Université Catholique de Louvain

Recombinant human deoxyribonuclease I (rhDNase) is the mucolytic agent most widely used in cystic fibrosis (CF) treatment. However, its rapid clearance from the lungs implies… (more)

Subjects/Keywords: Recombinant human deoxyribonuclease I; PEGylation; Cystic Fibrosis; Pulmonary drug delivery; Prolonged residence time

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APA (6th Edition):

Guichard, M. (2018). Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/197736

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):

Guichard, Marie-Julie. “Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease.” 2018. Thesis, Université Catholique de Louvain. Accessed October 30, 2020. http://hdl.handle.net/2078.1/197736.

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

MLA Handbook (7th Edition):

Guichard, Marie-Julie. “Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease.” 2018. Web. 30 Oct 2020.

Vancouver:

Guichard M. Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease. [Internet] [Thesis]. Université Catholique de Louvain; 2018. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2078.1/197736.

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

Council of Science Editors:

Guichard M. Development of a long-acting version of recombinant human deoxyribonuclease I for the treatment of cystic fibrosis lung disease. [Thesis]. Université Catholique de Louvain; 2018. Available from: http://hdl.handle.net/2078.1/197736

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


Universitat Ramon Llull

19. Boix Garriga, Ester. Biodegradable Poly(D,L-lactide) and Poly(D,L-lactide-co-glycolide) Nanoparticles for Photodynamic Therapy.

Degree: 2016, Universitat Ramon Llull

 This thesis reports the study of poly-(D,L-lactide-co-glycolide) (PLGA) and poly-(D,L-lactide) (PLA) nanoparticles and their poly-(ethylene glycol) (PEG)-coated counterparts as delivery systems for photosensitizers in photodynamic… (more)

Subjects/Keywords: Photodynamic therapy; PLGA nanoparticles; PEGylation; Singlet oxygen; Active targeting; Cancer; Ciències; 00; 5; 54; 544

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APA (6th Edition):

Boix Garriga, E. (2016). Biodegradable Poly(D,L-lactide) and Poly(D,L-lactide-co-glycolide) Nanoparticles for Photodynamic Therapy. (Thesis). Universitat Ramon Llull. Retrieved from http://hdl.handle.net/10803/368179

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):

Boix Garriga, Ester. “Biodegradable Poly(D,L-lactide) and Poly(D,L-lactide-co-glycolide) Nanoparticles for Photodynamic Therapy.” 2016. Thesis, Universitat Ramon Llull. Accessed October 30, 2020. http://hdl.handle.net/10803/368179.

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

MLA Handbook (7th Edition):

Boix Garriga, Ester. “Biodegradable Poly(D,L-lactide) and Poly(D,L-lactide-co-glycolide) Nanoparticles for Photodynamic Therapy.” 2016. Web. 30 Oct 2020.

Vancouver:

Boix Garriga E. Biodegradable Poly(D,L-lactide) and Poly(D,L-lactide-co-glycolide) Nanoparticles for Photodynamic Therapy. [Internet] [Thesis]. Universitat Ramon Llull; 2016. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10803/368179.

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

Council of Science Editors:

Boix Garriga E. Biodegradable Poly(D,L-lactide) and Poly(D,L-lactide-co-glycolide) Nanoparticles for Photodynamic Therapy. [Thesis]. Universitat Ramon Llull; 2016. Available from: http://hdl.handle.net/10803/368179

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


University of Manchester

20. Hu, Ping. Design of oxidation-sensitive polymer micelles for inflammation targeting.

Degree: PhD, 2012, University of Manchester

 The research presented in this thesis focuses on the molecular design of an oxidation-sensitive nanocarrier and its enzyme conjugate with a view of their application… (more)

Subjects/Keywords: 617.22; Block copolymer micelles; Polysulfides; Vinyl sulfone; FRET; Superoxide dismutase; PEGylation; Catalase

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APA (6th Edition):

Hu, P. (2012). Design of oxidation-sensitive polymer micelles for inflammation targeting. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/design-of-oxidationsensitive-polymer-micelles-for-inflammation-targeting(8ec02724-aeef-4ce8-ac2d-a3186de6267e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553419

Chicago Manual of Style (16th Edition):

Hu, Ping. “Design of oxidation-sensitive polymer micelles for inflammation targeting.” 2012. Doctoral Dissertation, University of Manchester. Accessed October 30, 2020. https://www.research.manchester.ac.uk/portal/en/theses/design-of-oxidationsensitive-polymer-micelles-for-inflammation-targeting(8ec02724-aeef-4ce8-ac2d-a3186de6267e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553419.

MLA Handbook (7th Edition):

Hu, Ping. “Design of oxidation-sensitive polymer micelles for inflammation targeting.” 2012. Web. 30 Oct 2020.

Vancouver:

Hu P. Design of oxidation-sensitive polymer micelles for inflammation targeting. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2020 Oct 30]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/design-of-oxidationsensitive-polymer-micelles-for-inflammation-targeting(8ec02724-aeef-4ce8-ac2d-a3186de6267e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553419.

Council of Science Editors:

Hu P. Design of oxidation-sensitive polymer micelles for inflammation targeting. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/design-of-oxidationsensitive-polymer-micelles-for-inflammation-targeting(8ec02724-aeef-4ce8-ac2d-a3186de6267e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.553419


Johannes Gutenberg Universität Mainz

21. Dingels, Carsten. Expanding the scope of poly(ethylene glycol)s for bioconjugation to squaric acid-mediated PEGylation and pH-sensitivity.

Degree: 2013, Johannes Gutenberg Universität Mainz

 Poly(ethylene glycol) (PEG) is used in a broad range of applications due to its unique combination of properties and is approved use in formulations for… (more)

Subjects/Keywords: Polyethylenglykol; PEGylierung; Quadratsäure; spaltbares PEG; Acetal; Poly(ethylene glycol); PEGylation; squaric acid; cleavable PEG; acetal; Chemistry and allied sciences

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APA (6th Edition):

Dingels, C. (2013). Expanding the scope of poly(ethylene glycol)s for bioconjugation to squaric acid-mediated PEGylation and pH-sensitivity. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2015/3930/

Chicago Manual of Style (16th Edition):

Dingels, Carsten. “Expanding the scope of poly(ethylene glycol)s for bioconjugation to squaric acid-mediated PEGylation and pH-sensitivity.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed October 30, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2015/3930/.

MLA Handbook (7th Edition):

Dingels, Carsten. “Expanding the scope of poly(ethylene glycol)s for bioconjugation to squaric acid-mediated PEGylation and pH-sensitivity.” 2013. Web. 30 Oct 2020.

Vancouver:

Dingels C. Expanding the scope of poly(ethylene glycol)s for bioconjugation to squaric acid-mediated PEGylation and pH-sensitivity. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2020 Oct 30]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/3930/.

Council of Science Editors:

Dingels C. Expanding the scope of poly(ethylene glycol)s for bioconjugation to squaric acid-mediated PEGylation and pH-sensitivity. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/3930/


Loyola University Chicago

22. Webster, Kyle Douglas. Development of "Inside-Out" Pegylated Crosslinked Hemoglobin Polymers: Novel Hemoglobin-Based Oxygen Carriers (HBOC).

Degree: PhD, Chemistry, 2016, Loyola University Chicago

  The development of an effective blood substitute is urgent due to increasingly common blood shortages, the need to type-match donated blood, and communicable diseases… (more)

Subjects/Keywords: Copper Free Azide-Alkyne Click Chemistry; Hemoglobin-Based Oxygen Carrier; Inside-Out PEGylation; Multi-Arm PEG; Thiol-Maleimide Click Chemistry; Biochemistry

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APA (6th Edition):

Webster, K. D. (2016). Development of "Inside-Out" Pegylated Crosslinked Hemoglobin Polymers: Novel Hemoglobin-Based Oxygen Carriers (HBOC). (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/1976

Chicago Manual of Style (16th Edition):

Webster, Kyle Douglas. “Development of "Inside-Out" Pegylated Crosslinked Hemoglobin Polymers: Novel Hemoglobin-Based Oxygen Carriers (HBOC).” 2016. Doctoral Dissertation, Loyola University Chicago. Accessed October 30, 2020. https://ecommons.luc.edu/luc_diss/1976.

MLA Handbook (7th Edition):

Webster, Kyle Douglas. “Development of "Inside-Out" Pegylated Crosslinked Hemoglobin Polymers: Novel Hemoglobin-Based Oxygen Carriers (HBOC).” 2016. Web. 30 Oct 2020.

Vancouver:

Webster KD. Development of "Inside-Out" Pegylated Crosslinked Hemoglobin Polymers: Novel Hemoglobin-Based Oxygen Carriers (HBOC). [Internet] [Doctoral dissertation]. Loyola University Chicago; 2016. [cited 2020 Oct 30]. Available from: https://ecommons.luc.edu/luc_diss/1976.

Council of Science Editors:

Webster KD. Development of "Inside-Out" Pegylated Crosslinked Hemoglobin Polymers: Novel Hemoglobin-Based Oxygen Carriers (HBOC). [Doctoral Dissertation]. Loyola University Chicago; 2016. Available from: https://ecommons.luc.edu/luc_diss/1976


McMaster University

23. Shang, Xiaojiao. Purification and synthesis of PEGylated protein.

Degree: PhD, 2013, McMaster University

PEGylation, referring to the covalent attachment of poly(ethylene glycol) or PEG to protein, has become the most established technology for improving pharmacokinetic behavior of… (more)

Subjects/Keywords: PEGylation; PEGylated protein; Membrane; Environment-responsive; Chromatography; Hydrophobic interaction; Polyethylene glycol; Hollow fibre; Chemical Engineering; Chemical Engineering

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APA (6th Edition):

Shang, X. (2013). Purification and synthesis of PEGylated protein. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/13637

Chicago Manual of Style (16th Edition):

Shang, Xiaojiao. “Purification and synthesis of PEGylated protein.” 2013. Doctoral Dissertation, McMaster University. Accessed October 30, 2020. http://hdl.handle.net/11375/13637.

MLA Handbook (7th Edition):

Shang, Xiaojiao. “Purification and synthesis of PEGylated protein.” 2013. Web. 30 Oct 2020.

Vancouver:

Shang X. Purification and synthesis of PEGylated protein. [Internet] [Doctoral dissertation]. McMaster University; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11375/13637.

Council of Science Editors:

Shang X. Purification and synthesis of PEGylated protein. [Doctoral Dissertation]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13637


Wayne State University

24. Wani, Amit S. Formulation Devlopment Of Mesoporous Silica Nanoparticles As An Injectable Delivery System.

Degree: PhD, Pharmaceutical Sciences, 2013, Wayne State University

  Our long term goal is to develop a versatile and robust injectable carrier based on Mesoporous Silica Nanoparticles (MSN) for drug/drug combination therapies. The… (more)

Subjects/Keywords: Drug Delivery; hydrophilic-hydrophobic drug combination; Injectable; Mesoporous Silica Nanoparticles; PEGylation; surface functionalization; Medicinal Chemistry and Pharmaceutics

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

APA (6th Edition):

Wani, A. S. (2013). Formulation Devlopment Of Mesoporous Silica Nanoparticles As An Injectable Delivery System. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/713

Chicago Manual of Style (16th Edition):

Wani, Amit S. “Formulation Devlopment Of Mesoporous Silica Nanoparticles As An Injectable Delivery System.” 2013. Doctoral Dissertation, Wayne State University. Accessed October 30, 2020. https://digitalcommons.wayne.edu/oa_dissertations/713.

MLA Handbook (7th Edition):

Wani, Amit S. “Formulation Devlopment Of Mesoporous Silica Nanoparticles As An Injectable Delivery System.” 2013. Web. 30 Oct 2020.

Vancouver:

Wani AS. Formulation Devlopment Of Mesoporous Silica Nanoparticles As An Injectable Delivery System. [Internet] [Doctoral dissertation]. Wayne State University; 2013. [cited 2020 Oct 30]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/713.

Council of Science Editors:

Wani AS. Formulation Devlopment Of Mesoporous Silica Nanoparticles As An Injectable Delivery System. [Doctoral Dissertation]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_dissertations/713


Wayne State University

25. Bharatwaj, Balaji. Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs.

Degree: PhD, Chemical Engineering and Materials Science, 2012, Wayne State University

  The lungs are considered as one of the fastest portals of entry to the bloodstream and oral inhalation (OI) has long been accepted as… (more)

Subjects/Keywords: Dendrimers, Oral Inhalation, PEGylation, Polymeric Nanocarriers, Pulmonary Drug Delivery, Transport Modulation; Chemical Engineering; Nanoscience and Nanotechnology

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APA (6th Edition):

Bharatwaj, B. (2012). Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/426

Chicago Manual of Style (16th Edition):

Bharatwaj, Balaji. “Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs.” 2012. Doctoral Dissertation, Wayne State University. Accessed October 30, 2020. https://digitalcommons.wayne.edu/oa_dissertations/426.

MLA Handbook (7th Edition):

Bharatwaj, Balaji. “Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs.” 2012. Web. 30 Oct 2020.

Vancouver:

Bharatwaj B. Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs. [Internet] [Doctoral dissertation]. Wayne State University; 2012. [cited 2020 Oct 30]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/426.

Council of Science Editors:

Bharatwaj B. Polymeric nanocarriers for the regional and systemic delivery of therapeutics to and through the lungs. [Doctoral Dissertation]. Wayne State University; 2012. Available from: https://digitalcommons.wayne.edu/oa_dissertations/426


University of KwaZulu-Natal

26. Daniels, Aliscia Nicole. Functionalised gold nanoparticle delivery for c-MYC siRNA in cancer gene therapy.

Degree: 2018, University of KwaZulu-Natal

Abstract available in PDF file. Advisors/Committee Members: Singh, Moganavelli. (advisor), Singh, Sooboo. (advisor).

Subjects/Keywords: Theses - Biochemistry.; PEGylation.; Gene silencing.; Cytotoxicity.; Gold nanoparticles.

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APA (6th Edition):

Daniels, A. N. (2018). Functionalised gold nanoparticle delivery for c-MYC siRNA in cancer gene therapy. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/16248

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):

Daniels, Aliscia Nicole. “Functionalised gold nanoparticle delivery for c-MYC siRNA in cancer gene therapy.” 2018. Thesis, University of KwaZulu-Natal. Accessed October 30, 2020. https://researchspace.ukzn.ac.za/handle/10413/16248.

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

MLA Handbook (7th Edition):

Daniels, Aliscia Nicole. “Functionalised gold nanoparticle delivery for c-MYC siRNA in cancer gene therapy.” 2018. Web. 30 Oct 2020.

Vancouver:

Daniels AN. Functionalised gold nanoparticle delivery for c-MYC siRNA in cancer gene therapy. [Internet] [Thesis]. University of KwaZulu-Natal; 2018. [cited 2020 Oct 30]. Available from: https://researchspace.ukzn.ac.za/handle/10413/16248.

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

Council of Science Editors:

Daniels AN. Functionalised gold nanoparticle delivery for c-MYC siRNA in cancer gene therapy. [Thesis]. University of KwaZulu-Natal; 2018. Available from: https://researchspace.ukzn.ac.za/handle/10413/16248

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


University of KwaZulu-Natal

27. Balgobind, Adhika. The silencing of HER2/neu gene expression in a breast cancer cell model using cationic lipid based delivery systems.

Degree: 2016, University of KwaZulu-Natal

Abstract available in PDF file. Advisors/Committee Members: Singh, Moganavelli. (advisor), Ariatti, Mario. (advisor).

Subjects/Keywords: Theses - Biological Sciences.; Breast Cancer.; Cationic lipids.; Pegylation.

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APA (6th Edition):

Balgobind, A. (2016). The silencing of HER2/neu gene expression in a breast cancer cell model using cationic lipid based delivery systems. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/16059

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):

Balgobind, Adhika. “The silencing of HER2/neu gene expression in a breast cancer cell model using cationic lipid based delivery systems.” 2016. Thesis, University of KwaZulu-Natal. Accessed October 30, 2020. http://hdl.handle.net/10413/16059.

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

MLA Handbook (7th Edition):

Balgobind, Adhika. “The silencing of HER2/neu gene expression in a breast cancer cell model using cationic lipid based delivery systems.” 2016. Web. 30 Oct 2020.

Vancouver:

Balgobind A. The silencing of HER2/neu gene expression in a breast cancer cell model using cationic lipid based delivery systems. [Internet] [Thesis]. University of KwaZulu-Natal; 2016. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10413/16059.

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

Council of Science Editors:

Balgobind A. The silencing of HER2/neu gene expression in a breast cancer cell model using cationic lipid based delivery systems. [Thesis]. University of KwaZulu-Natal; 2016. Available from: http://hdl.handle.net/10413/16059

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


Universidade Nova

28. Pereira, Mafalda Maria Robalo de Azevedo Aleixo. Role of sympathetic innervation in obesity.

Degree: 2015, Universidade Nova

Part of the results presented in this thesis were published in the following reference (DOI 10.1016/j.cell.2015.08.055): Wenwen Zeng*, Roksana M. Pirzgalska*, Mafalda M.A. Pereira, Nadiya… (more)

Subjects/Keywords: Obesity; Sympathetic nervous system; PEGylation; Amphetamine; Anatomy; Adipose organ; Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química

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APA (6th Edition):

Pereira, M. M. R. d. A. A. (2015). Role of sympathetic innervation in obesity. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15841

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):

Pereira, Mafalda Maria Robalo de Azevedo Aleixo. “Role of sympathetic innervation in obesity.” 2015. Thesis, Universidade Nova. Accessed October 30, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15841.

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

MLA Handbook (7th Edition):

Pereira, Mafalda Maria Robalo de Azevedo Aleixo. “Role of sympathetic innervation in obesity.” 2015. Web. 30 Oct 2020.

Vancouver:

Pereira MMRdAA. Role of sympathetic innervation in obesity. [Internet] [Thesis]. Universidade Nova; 2015. [cited 2020 Oct 30]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15841.

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

Council of Science Editors:

Pereira MMRdAA. Role of sympathetic innervation in obesity. [Thesis]. Universidade Nova; 2015. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/15841

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


University of Miami

29. Finn, Kristina Kateri. Cellular Encapsulation Techniques: Camouflaging Islet Cells from the Immune and Inflammatory Responses Associated with Islet Transplantation.

Degree: MS, Biomedical Engineering (Engineering), 2008, University of Miami

  Diabetes is a debilitating disease affecting millions of people worldwide. The transplantation of insulin-producing, pancreatic islet cells has been an extensively explored approach for… (more)

Subjects/Keywords: Diabetes Mellitus; Islet Transplantation; Covalent Crosslinking; PEGylation; Microencapsulation

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APA (6th Edition):

Finn, K. K. (2008). Cellular Encapsulation Techniques: Camouflaging Islet Cells from the Immune and Inflammatory Responses Associated with Islet Transplantation. (Thesis). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_theses/231

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):

Finn, Kristina Kateri. “Cellular Encapsulation Techniques: Camouflaging Islet Cells from the Immune and Inflammatory Responses Associated with Islet Transplantation.” 2008. Thesis, University of Miami. Accessed October 30, 2020. https://scholarlyrepository.miami.edu/oa_theses/231.

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

MLA Handbook (7th Edition):

Finn, Kristina Kateri. “Cellular Encapsulation Techniques: Camouflaging Islet Cells from the Immune and Inflammatory Responses Associated with Islet Transplantation.” 2008. Web. 30 Oct 2020.

Vancouver:

Finn KK. Cellular Encapsulation Techniques: Camouflaging Islet Cells from the Immune and Inflammatory Responses Associated with Islet Transplantation. [Internet] [Thesis]. University of Miami; 2008. [cited 2020 Oct 30]. Available from: https://scholarlyrepository.miami.edu/oa_theses/231.

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

Council of Science Editors:

Finn KK. Cellular Encapsulation Techniques: Camouflaging Islet Cells from the Immune and Inflammatory Responses Associated with Islet Transplantation. [Thesis]. University of Miami; 2008. Available from: https://scholarlyrepository.miami.edu/oa_theses/231

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


University of Manchester

30. Cadman, Christopher. Titanium dioxide nanoparticles for photodynamic therapy.

Degree: PhD, 2013, University of Manchester

 In the present thesis we propose the development of hybrid polymer titanium dioxide (TiO2) nanoparticles for use in biomedical applications. TiO2 exhibits high biocompatibility in… (more)

Subjects/Keywords: 620; Titanium dioxide nanoparticles; Photodynamic therapy; Sol-gel synthesis; PEGylation; Adsorption; Poly electrolyte multiwalled microspheres; Catechols; Phosphonates

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

APA (6th Edition):

Cadman, C. (2013). Titanium dioxide nanoparticles for photodynamic therapy. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/titanium-dioxide-nanoparticles-for-photodynamic-therapy(91717f00-c70e-4f07-8921-64caa9290b42).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.576852

Chicago Manual of Style (16th Edition):

Cadman, Christopher. “Titanium dioxide nanoparticles for photodynamic therapy.” 2013. Doctoral Dissertation, University of Manchester. Accessed October 30, 2020. https://www.research.manchester.ac.uk/portal/en/theses/titanium-dioxide-nanoparticles-for-photodynamic-therapy(91717f00-c70e-4f07-8921-64caa9290b42).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.576852.

MLA Handbook (7th Edition):

Cadman, Christopher. “Titanium dioxide nanoparticles for photodynamic therapy.” 2013. Web. 30 Oct 2020.

Vancouver:

Cadman C. Titanium dioxide nanoparticles for photodynamic therapy. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Oct 30]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/titanium-dioxide-nanoparticles-for-photodynamic-therapy(91717f00-c70e-4f07-8921-64caa9290b42).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.576852.

Council of Science Editors:

Cadman C. Titanium dioxide nanoparticles for photodynamic therapy. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/titanium-dioxide-nanoparticles-for-photodynamic-therapy(91717f00-c70e-4f07-8921-64caa9290b42).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.576852

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