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You searched for subject:(drug conjugate). Showing records 1 – 25 of 25 total matches.

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University of Waterloo

1. Won, Gah-Jone. The Development of an Antibody-Drug Conjugate to Specifically Target and Soften the Crystalline Lens in vivo.

Degree: 2017, University of Waterloo

 Helmholtz’s classical theory of accommodation states that, within the eye, contraction of the annular ciliary muscle releases the passive tension of zonules that hold the… (more)

Subjects/Keywords: Crystalline Lens; Presbyopia; Antibody-Drug Conjugate

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APA (6th Edition):

Won, G. (2017). The Development of an Antibody-Drug Conjugate to Specifically Target and Soften the Crystalline Lens in vivo. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/11628

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):

Won, Gah-Jone. “The Development of an Antibody-Drug Conjugate to Specifically Target and Soften the Crystalline Lens in vivo.” 2017. Thesis, University of Waterloo. Accessed June 20, 2019. http://hdl.handle.net/10012/11628.

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

MLA Handbook (7th Edition):

Won, Gah-Jone. “The Development of an Antibody-Drug Conjugate to Specifically Target and Soften the Crystalline Lens in vivo.” 2017. Web. 20 Jun 2019.

Vancouver:

Won G. The Development of an Antibody-Drug Conjugate to Specifically Target and Soften the Crystalline Lens in vivo. [Internet] [Thesis]. University of Waterloo; 2017. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10012/11628.

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

Council of Science Editors:

Won G. The Development of an Antibody-Drug Conjugate to Specifically Target and Soften the Crystalline Lens in vivo. [Thesis]. University of Waterloo; 2017. Available from: http://hdl.handle.net/10012/11628

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


McMaster University

2. Vanner, Stephanie. Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies.

Degree: MSc, 2014, McMaster University

Natural products are an important resource for cancer therapy, with highly potent and diverse anticancer activities. Natural product biosynthesis is well comprehended, however the evolutionary… (more)

Subjects/Keywords: natural product; antibody-drug conjugate; cancer

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APA (6th Edition):

Vanner, S. (2014). Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15390

Chicago Manual of Style (16th Edition):

Vanner, Stephanie. “Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies.” 2014. Masters Thesis, McMaster University. Accessed June 20, 2019. http://hdl.handle.net/11375/15390.

MLA Handbook (7th Edition):

Vanner, Stephanie. “Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies.” 2014. Web. 20 Jun 2019.

Vancouver:

Vanner S. Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/11375/15390.

Council of Science Editors:

Vanner S. Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/15390


University of Notre Dame

3. Cheng Ji. Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>.

Degree: PhD, Chemistry and Biochemistry, 2012, University of Notre Dame

  Siderophores are an important class of natural products that have received wide attention for many years due to their unique properties as microbial iron… (more)

Subjects/Keywords: siderophore; antibiotics; linkers; drug-conjugate; pathogen detection

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APA (6th Edition):

Ji, C. (2012). Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/9w032229q13

Chicago Manual of Style (16th Edition):

Ji, Cheng. “Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed June 20, 2019. https://curate.nd.edu/show/9w032229q13.

MLA Handbook (7th Edition):

Ji, Cheng. “Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>.” 2012. Web. 20 Jun 2019.

Vancouver:

Ji C. Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Jun 20]. Available from: https://curate.nd.edu/show/9w032229q13.

Council of Science Editors:

Ji C. Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/9w032229q13


University of Notre Dame

4. Raúl Erick Juá‡rez Hernández. A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>.

Degree: PhD, Chemistry and Biochemistry, 2012, University of Notre Dame

  Siderophores are extremely versatile molecules synthesized by a variety of organisms with the objective of gathering iron, an essential element for most of living… (more)

Subjects/Keywords: desferrioxamine B; drug-conjugate; mycobactin; siderophore; sideromycin

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APA (6th Edition):

Hernández, R. E. J. (2012). A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/ft848p60v7m

Chicago Manual of Style (16th Edition):

Hernández, Raúl Erick Juá‡rez. “A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed June 20, 2019. https://curate.nd.edu/show/ft848p60v7m.

MLA Handbook (7th Edition):

Hernández, Raúl Erick Juá‡rez. “A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>.” 2012. Web. 20 Jun 2019.

Vancouver:

Hernández REJ. A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Jun 20]. Available from: https://curate.nd.edu/show/ft848p60v7m.

Council of Science Editors:

Hernández REJ. A Convergent Approach for the Syntheses of Sideromycins: Mycobactin T and Gallioxamine B Conjugates</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/ft848p60v7m


Université Catholique de Louvain

5. Luo, Tian. PEGylation of paclitaxel for inhaled chemotherapy.

Degree: 2016, Université Catholique de Louvain

Pulmonary delivery offers an attractive route for delivering chemotherapeutics, with the benefits of high drug concentrations locally and low side effects systemically. However, fast clearance… (more)

Subjects/Keywords: Pulmonary delivery; Lung cancer; Polymer-drug conjugate; Paclitaxel

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APA (6th Edition):

Luo, T. (2016). PEGylation of paclitaxel for inhaled chemotherapy. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/175656

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):

Luo, Tian. “PEGylation of paclitaxel for inhaled chemotherapy.” 2016. Thesis, Université Catholique de Louvain. Accessed June 20, 2019. http://hdl.handle.net/2078.1/175656.

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

MLA Handbook (7th Edition):

Luo, Tian. “PEGylation of paclitaxel for inhaled chemotherapy.” 2016. Web. 20 Jun 2019.

Vancouver:

Luo T. PEGylation of paclitaxel for inhaled chemotherapy. [Internet] [Thesis]. Université Catholique de Louvain; 2016. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2078.1/175656.

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

Council of Science Editors:

Luo T. PEGylation of paclitaxel for inhaled chemotherapy. [Thesis]. Université Catholique de Louvain; 2016. Available from: http://hdl.handle.net/2078.1/175656

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

6. [No author]. The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers .

Degree: 2016, Washington State University

 During the development of a series of phosphoramidate-based inhibitors to prostate-specific membrane antigen, we observed a trend in increasing acid stability as the distance between… (more)

Subjects/Keywords: Organic chemistry; Cleavable linker; Drug conjugate; Drug delivery; Phosphoramidate; pH-tunable; Prostate-specific membrane antigen

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APA (6th Edition):

author], [. (2016). The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers . (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/12074

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):

author], [No. “The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers .” 2016. Thesis, Washington State University. Accessed June 20, 2019. http://hdl.handle.net/2376/12074.

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

MLA Handbook (7th Edition):

author], [No. “The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers .” 2016. Web. 20 Jun 2019.

Vancouver:

author] [. The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers . [Internet] [Thesis]. Washington State University; 2016. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2376/12074.

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

Council of Science Editors:

author] [. The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers . [Thesis]. Washington State University; 2016. Available from: http://hdl.handle.net/2376/12074

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

7. Pusuluri, Anusha. Aptamer targeted delivery of synergistic drug combinations for effective cancer therapy.

Degree: 2018, University of California – eScholarship, University of California

 Potent chemotherapy combinations identified and optimized in vitro often fail in clinic because the current paradigm aims to deliver drugs at or near their maximum… (more)

Subjects/Keywords: Bioengineering; Nanotechnology; Oncology; aptamer drug conjugate; breast cancer; peptide scaffolds; ratiometric drug loading; synergy; targeted drug delivery

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APA (6th Edition):

Pusuluri, A. (2018). Aptamer targeted delivery of synergistic drug combinations for effective cancer therapy. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/8fp6m143

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):

Pusuluri, Anusha. “Aptamer targeted delivery of synergistic drug combinations for effective cancer therapy.” 2018. Thesis, University of California – eScholarship, University of California. Accessed June 20, 2019. http://www.escholarship.org/uc/item/8fp6m143.

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

MLA Handbook (7th Edition):

Pusuluri, Anusha. “Aptamer targeted delivery of synergistic drug combinations for effective cancer therapy.” 2018. Web. 20 Jun 2019.

Vancouver:

Pusuluri A. Aptamer targeted delivery of synergistic drug combinations for effective cancer therapy. [Internet] [Thesis]. University of California – eScholarship, University of California; 2018. [cited 2019 Jun 20]. Available from: http://www.escholarship.org/uc/item/8fp6m143.

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

Council of Science Editors:

Pusuluri A. Aptamer targeted delivery of synergistic drug combinations for effective cancer therapy. [Thesis]. University of California – eScholarship, University of California; 2018. Available from: http://www.escholarship.org/uc/item/8fp6m143

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


Uppsala University

8. Congreve, Samantha; Elias, Reham Faris; Tidestav, Gabriel. Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs.

Degree: Engineering Sciences, 2018, Uppsala University

  A literature study was performed on a new type of cancer medicine: antibody drug conjugates, or ADCs. These consist of a monoclonal antibody, chemically… (more)

Subjects/Keywords: ADC; antibody; drug; conjugate; biopharmaceuticals; structure; linker; payload; target; conjugation; market; Chemical Engineering; Kemiteknik

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APA (6th Edition):

Congreve, Samantha; Elias, Reham Faris; Tidestav, G. (2018). Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917

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):

Congreve, Samantha; Elias, Reham Faris; Tidestav, Gabriel. “Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs.” 2018. Thesis, Uppsala University. Accessed June 20, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917.

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

MLA Handbook (7th Edition):

Congreve, Samantha; Elias, Reham Faris; Tidestav, Gabriel. “Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs.” 2018. Web. 20 Jun 2019.

Vancouver:

Congreve, Samantha; Elias, Reham Faris; Tidestav G. Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs. [Internet] [Thesis]. Uppsala University; 2018. [cited 2019 Jun 20]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917.

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

Council of Science Editors:

Congreve, Samantha; Elias, Reham Faris; Tidestav G. Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs. [Thesis]. Uppsala University; 2018. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917

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


University of Toronto

9. Hu, Sally. Investigating In Vivo Efficacy of Novel ALN-EP4a Conjugate Drugs for the Treatment of Post-menopausal Osteoporosis.

Degree: 2014, University of Toronto

Current treatments for post-menopausal osteoporosis are mainly anti-resorptive, which decrease osteoclastic bone resorption but show little bone-building effects to reverse bone loss. The current study… (more)

Subjects/Keywords: Anabolic Bone Therapy; Animal Model; Biomechanics; Bone biology; Conjugate Drug; Osteoporosis; 0571

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APA (6th Edition):

Hu, S. (2014). Investigating In Vivo Efficacy of Novel ALN-EP4a Conjugate Drugs for the Treatment of Post-menopausal Osteoporosis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68507

Chicago Manual of Style (16th Edition):

Hu, Sally. “Investigating In Vivo Efficacy of Novel ALN-EP4a Conjugate Drugs for the Treatment of Post-menopausal Osteoporosis.” 2014. Masters Thesis, University of Toronto. Accessed June 20, 2019. http://hdl.handle.net/1807/68507.

MLA Handbook (7th Edition):

Hu, Sally. “Investigating In Vivo Efficacy of Novel ALN-EP4a Conjugate Drugs for the Treatment of Post-menopausal Osteoporosis.” 2014. Web. 20 Jun 2019.

Vancouver:

Hu S. Investigating In Vivo Efficacy of Novel ALN-EP4a Conjugate Drugs for the Treatment of Post-menopausal Osteoporosis. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1807/68507.

Council of Science Editors:

Hu S. Investigating In Vivo Efficacy of Novel ALN-EP4a Conjugate Drugs for the Treatment of Post-menopausal Osteoporosis. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68507

10. Varini, Karine. Trafic intracellulaire de peptide-vecteurs ciblant le récepteur au LDL pour des stratégies de délivrance ciblée d'agents thérapeutiques ou d'imagerie à travers la barrière hémato-encéphalique : Intracellular trafficking of peptide-vectors that target the LDL receptor for the delivery of imaging or therapeutic agents across the blood brain barrier.

Degree: Docteur es, Neurosciences, 2015, Aix Marseille Université

La plupart des médicaments développés pour les maladies du SNC n’atteignent pas leur cible en raison des propriétés uniques de la BHE, nécessitant la mise… (more)

Subjects/Keywords: Bhe; Rmt; Peptide-Vecteur; Conjugué vecteur-Candidat médicament; Bbb; Rmt; Peptide-Vector; Drug-Conjugate

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APA (6th Edition):

Varini, K. (2015). Trafic intracellulaire de peptide-vecteurs ciblant le récepteur au LDL pour des stratégies de délivrance ciblée d'agents thérapeutiques ou d'imagerie à travers la barrière hémato-encéphalique : Intracellular trafficking of peptide-vectors that target the LDL receptor for the delivery of imaging or therapeutic agents across the blood brain barrier. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2015AIXM5023

Chicago Manual of Style (16th Edition):

Varini, Karine. “Trafic intracellulaire de peptide-vecteurs ciblant le récepteur au LDL pour des stratégies de délivrance ciblée d'agents thérapeutiques ou d'imagerie à travers la barrière hémato-encéphalique : Intracellular trafficking of peptide-vectors that target the LDL receptor for the delivery of imaging or therapeutic agents across the blood brain barrier.” 2015. Doctoral Dissertation, Aix Marseille Université. Accessed June 20, 2019. http://www.theses.fr/2015AIXM5023.

MLA Handbook (7th Edition):

Varini, Karine. “Trafic intracellulaire de peptide-vecteurs ciblant le récepteur au LDL pour des stratégies de délivrance ciblée d'agents thérapeutiques ou d'imagerie à travers la barrière hémato-encéphalique : Intracellular trafficking of peptide-vectors that target the LDL receptor for the delivery of imaging or therapeutic agents across the blood brain barrier.” 2015. Web. 20 Jun 2019.

Vancouver:

Varini K. Trafic intracellulaire de peptide-vecteurs ciblant le récepteur au LDL pour des stratégies de délivrance ciblée d'agents thérapeutiques ou d'imagerie à travers la barrière hémato-encéphalique : Intracellular trafficking of peptide-vectors that target the LDL receptor for the delivery of imaging or therapeutic agents across the blood brain barrier. [Internet] [Doctoral dissertation]. Aix Marseille Université 2015. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2015AIXM5023.

Council of Science Editors:

Varini K. Trafic intracellulaire de peptide-vecteurs ciblant le récepteur au LDL pour des stratégies de délivrance ciblée d'agents thérapeutiques ou d'imagerie à travers la barrière hémato-encéphalique : Intracellular trafficking of peptide-vectors that target the LDL receptor for the delivery of imaging or therapeutic agents across the blood brain barrier. [Doctoral Dissertation]. Aix Marseille Université 2015. Available from: http://www.theses.fr/2015AIXM5023


University of Lund

11. Menard, Julien. Adaptive mechanisms in the hypoxic tumor microenvironment. Functional role of proteoglycans and identification of potential treatment targets.

Degree: 2017, University of Lund

 Cancer cells reside in a complex microenvironment comprising stromal cells and immune cells embedded in an extracellular matrix (ECM). Early on in tumor progression, cells… (more)

Subjects/Keywords: Medicin och hälsovetenskap; Hypoxia; Acidosis; Proteoglycans; Endocytosis; Glioblastoma; Lipid; Caveolin-1; Antibody-drug conjugate

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APA (6th Edition):

Menard, J. (2017). Adaptive mechanisms in the hypoxic tumor microenvironment. Functional role of proteoglycans and identification of potential treatment targets. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/ee8405ce-c9c0-46e7-a784-a754d7db14ad ; http://portal.research.lu.se/ws/files/33514239/Julien_Menard_Thesis_kappa.pdf

Chicago Manual of Style (16th Edition):

Menard, Julien. “Adaptive mechanisms in the hypoxic tumor microenvironment. Functional role of proteoglycans and identification of potential treatment targets.” 2017. Doctoral Dissertation, University of Lund. Accessed June 20, 2019. http://lup.lub.lu.se/record/ee8405ce-c9c0-46e7-a784-a754d7db14ad ; http://portal.research.lu.se/ws/files/33514239/Julien_Menard_Thesis_kappa.pdf.

MLA Handbook (7th Edition):

Menard, Julien. “Adaptive mechanisms in the hypoxic tumor microenvironment. Functional role of proteoglycans and identification of potential treatment targets.” 2017. Web. 20 Jun 2019.

Vancouver:

Menard J. Adaptive mechanisms in the hypoxic tumor microenvironment. Functional role of proteoglycans and identification of potential treatment targets. [Internet] [Doctoral dissertation]. University of Lund; 2017. [cited 2019 Jun 20]. Available from: http://lup.lub.lu.se/record/ee8405ce-c9c0-46e7-a784-a754d7db14ad ; http://portal.research.lu.se/ws/files/33514239/Julien_Menard_Thesis_kappa.pdf.

Council of Science Editors:

Menard J. Adaptive mechanisms in the hypoxic tumor microenvironment. Functional role of proteoglycans and identification of potential treatment targets. [Doctoral Dissertation]. University of Lund; 2017. Available from: http://lup.lub.lu.se/record/ee8405ce-c9c0-46e7-a784-a754d7db14ad ; http://portal.research.lu.se/ws/files/33514239/Julien_Menard_Thesis_kappa.pdf


Northeastern University

12. Mandapati, Savitri. Preparation and characterization of polymer-multi drug conjugate delivery system for efficient cancer therapy.

Degree: MS, Department of Pharmaceutical Sciences, 2010, Northeastern University

 The aim of this study is to prepare and characterize polymer drug-conjugate delivery system loaded with doxorubicin and melphalan for successful passive or active targeting… (more)

Subjects/Keywords: pharmaceutical sciences; cancer therapy; polymer-multi drug conjugate delivery system; Cancer - Treatment; Drug delivery systems; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Mandapati, S. (2010). Preparation and characterization of polymer-multi drug conjugate delivery system for efficient cancer therapy. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20000985

Chicago Manual of Style (16th Edition):

Mandapati, Savitri. “Preparation and characterization of polymer-multi drug conjugate delivery system for efficient cancer therapy.” 2010. Masters Thesis, Northeastern University. Accessed June 20, 2019. http://hdl.handle.net/2047/d20000985.

MLA Handbook (7th Edition):

Mandapati, Savitri. “Preparation and characterization of polymer-multi drug conjugate delivery system for efficient cancer therapy.” 2010. Web. 20 Jun 2019.

Vancouver:

Mandapati S. Preparation and characterization of polymer-multi drug conjugate delivery system for efficient cancer therapy. [Internet] [Masters thesis]. Northeastern University; 2010. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2047/d20000985.

Council of Science Editors:

Mandapati S. Preparation and characterization of polymer-multi drug conjugate delivery system for efficient cancer therapy. [Masters Thesis]. Northeastern University; 2010. Available from: http://hdl.handle.net/2047/d20000985

13. Saxena, Rubha. Synthesis, characterization and biological evaluation of a polymeric drug conjugate for cancer chemotherapy;.

Degree: Pharmacy, 2014, JSS University

None

Reference p. 114-127

Advisors/Committee Members: Nanjan, M J.

Subjects/Keywords: Cancer chemotherapy; Polymeric drug conjugate; Thermo responsive polymeric carriers

Page 1

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APA (6th Edition):

Saxena, R. (2014). Synthesis, characterization and biological evaluation of a polymeric drug conjugate for cancer chemotherapy;. (Thesis). JSS University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/30858

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):

Saxena, Rubha. “Synthesis, characterization and biological evaluation of a polymeric drug conjugate for cancer chemotherapy;.” 2014. Thesis, JSS University. Accessed June 20, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/30858.

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

MLA Handbook (7th Edition):

Saxena, Rubha. “Synthesis, characterization and biological evaluation of a polymeric drug conjugate for cancer chemotherapy;.” 2014. Web. 20 Jun 2019.

Vancouver:

Saxena R. Synthesis, characterization and biological evaluation of a polymeric drug conjugate for cancer chemotherapy;. [Internet] [Thesis]. JSS University; 2014. [cited 2019 Jun 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/30858.

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

Council of Science Editors:

Saxena R. Synthesis, characterization and biological evaluation of a polymeric drug conjugate for cancer chemotherapy;. [Thesis]. JSS University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/30858

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


University of Michigan

14. Cilliers, Cornelius. Improving Antibody-drug Conjugate Tumor Distribution and Efficacy Using Single-Cell Imaging and Multiscale Modeling.

Degree: PhD, Chemical Engineering, 2018, University of Michigan

 Antibody-drug conjugates (ADCs) are a targeted cancer therapy combining the tumor cell specificity of antibodies with small-molecule chemotherapy. Despite the widespread use of ADC therapeutics,… (more)

Subjects/Keywords: Antibody-drug conjugate (ADC); Antibody Tumor Distribution; Multiscale Tissue Modeling; Antibody pharmacokinetics/pharmacodynamics; Chemical Engineering; Engineering

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

APA (6th Edition):

Cilliers, C. (2018). Improving Antibody-drug Conjugate Tumor Distribution and Efficacy Using Single-Cell Imaging and Multiscale Modeling. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/147665

Chicago Manual of Style (16th Edition):

Cilliers, Cornelius. “Improving Antibody-drug Conjugate Tumor Distribution and Efficacy Using Single-Cell Imaging and Multiscale Modeling.” 2018. Doctoral Dissertation, University of Michigan. Accessed June 20, 2019. http://hdl.handle.net/2027.42/147665.

MLA Handbook (7th Edition):

Cilliers, Cornelius. “Improving Antibody-drug Conjugate Tumor Distribution and Efficacy Using Single-Cell Imaging and Multiscale Modeling.” 2018. Web. 20 Jun 2019.

Vancouver:

Cilliers C. Improving Antibody-drug Conjugate Tumor Distribution and Efficacy Using Single-Cell Imaging and Multiscale Modeling. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2027.42/147665.

Council of Science Editors:

Cilliers C. Improving Antibody-drug Conjugate Tumor Distribution and Efficacy Using Single-Cell Imaging and Multiscale Modeling. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/147665


University of Oxford

15. Yamamoto, Keisuke. Modification and application of glycosidases to create homogeneous glycoconjugates.

Degree: PhD, 2013, University of Oxford

 In the post-genomic era, recognition of the importance of sugars is increasing in biological research. For the precise analysis of their functions, homogeneous materials are… (more)

Subjects/Keywords: 572.567; Organic chemistry; Chemical biology; Enzymes; Biomimetic synthesis; Protein chemistry; Glycobiology; glycosidase; oligosaccharide; glycoprotein; glycosynthase; endo-beta-N-acetylglucosaminidase; antibody-drug conjugate; glycan trimming

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APA (6th Edition):

Yamamoto, K. (2013). Modification and application of glycosidases to create homogeneous glycoconjugates. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:59d1917c-345d-4fe3-ace4-67dd3c8bc017 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581357

Chicago Manual of Style (16th Edition):

Yamamoto, Keisuke. “Modification and application of glycosidases to create homogeneous glycoconjugates.” 2013. Doctoral Dissertation, University of Oxford. Accessed June 20, 2019. http://ora.ox.ac.uk/objects/uuid:59d1917c-345d-4fe3-ace4-67dd3c8bc017 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581357.

MLA Handbook (7th Edition):

Yamamoto, Keisuke. “Modification and application of glycosidases to create homogeneous glycoconjugates.” 2013. Web. 20 Jun 2019.

Vancouver:

Yamamoto K. Modification and application of glycosidases to create homogeneous glycoconjugates. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Jun 20]. Available from: http://ora.ox.ac.uk/objects/uuid:59d1917c-345d-4fe3-ace4-67dd3c8bc017 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581357.

Council of Science Editors:

Yamamoto K. Modification and application of glycosidases to create homogeneous glycoconjugates. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:59d1917c-345d-4fe3-ace4-67dd3c8bc017 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581357


University of Debrecen

16. Krog, Magnus Aarnes. Trastuzumab Emtansine A New Antibody Directed Cytotoxic Drug Against HER2-Positive Breast Cancer .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Trastuzumab emtansine (Kadcyla®) is a new drug used as a second-line agent in patients with HER2-positive metastatic breast cancer previously treated with trastuzumab and a… (more)

Subjects/Keywords: Trastuzumab emtansine; Kadcyla; Antibody drug conjugate; HER 2 positive breast cancer

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

APA (6th Edition):

Krog, M. A. (n.d.). Trastuzumab Emtansine A New Antibody Directed Cytotoxic Drug Against HER2-Positive Breast Cancer . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/230515

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

Chicago Manual of Style (16th Edition):

Krog, Magnus Aarnes. “Trastuzumab Emtansine A New Antibody Directed Cytotoxic Drug Against HER2-Positive Breast Cancer .” Thesis, University of Debrecen. Accessed June 20, 2019. http://hdl.handle.net/2437/230515.

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

MLA Handbook (7th Edition):

Krog, Magnus Aarnes. “Trastuzumab Emtansine A New Antibody Directed Cytotoxic Drug Against HER2-Positive Breast Cancer .” Web. 20 Jun 2019.

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

Vancouver:

Krog MA. Trastuzumab Emtansine A New Antibody Directed Cytotoxic Drug Against HER2-Positive Breast Cancer . [Internet] [Thesis]. University of Debrecen; [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2437/230515.

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

Council of Science Editors:

Krog MA. Trastuzumab Emtansine A New Antibody Directed Cytotoxic Drug Against HER2-Positive Breast Cancer . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/230515

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

17. Goeij, Bart Egbertus Cornelis Gijsbertus de. Antibody-drug conjugates in cancer.

Degree: 2016, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University

 Antibody drug conjugates (ADCs) are emerging as powerful anti-cancer treatments. They are designed to combine the tumor specificity, pharmacokinetics and biodistribution properties of antibodies with… (more)

Subjects/Keywords: Monoclonal antibody; Antibody-drug conjugate; Bispecific antibody; Tissue factor; HER2; kappa-ETA'; Monoclonal antibody; Antibody-drug conjugate; Bispecific antibody; Tissue factor; HER2; kappa-ETA'

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APA (6th Edition):

Goeij, B. E. C. G. d. (2016). Antibody-drug conjugates in cancer. (Doctoral Dissertation). Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/38737

Chicago Manual of Style (16th Edition):

Goeij, Bart Egbertus Cornelis Gijsbertus de. “Antibody-drug conjugates in cancer.” 2016. Doctoral Dissertation, Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University. Accessed June 20, 2019. http://hdl.handle.net/1887/38737.

MLA Handbook (7th Edition):

Goeij, Bart Egbertus Cornelis Gijsbertus de. “Antibody-drug conjugates in cancer.” 2016. Web. 20 Jun 2019.

Vancouver:

Goeij BECGd. Antibody-drug conjugates in cancer. [Internet] [Doctoral dissertation]. Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2016. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1887/38737.

Council of Science Editors:

Goeij BECGd. Antibody-drug conjugates in cancer. [Doctoral Dissertation]. Faculty of Medicine, Leiden University Medical Center (LUMC), Leiden University; 2016. Available from: http://hdl.handle.net/1887/38737


Universitat de Barcelona

18. Plà Solans, Helena. Design, synthesis and biological evaluation of new polymer-drug conjugates based on polyglutamic acid and 5-Fluorouracil for the treatment of advanced colorectal cancer.

Degree: 2014, Universitat de Barcelona

 El agente 5-fluorouracilo (5-FU) es el tratamiento quimioterapéutico sistémico esencial para el tratamiento del cáncer colorectal. Sin embargo, la supervivencia global y superación de la… (more)

Subjects/Keywords: Càncer colorectal; Cáncer colorectal; Colorectal cancer; Disseny de medicaments; Diseño de medicamentos; Drug design; Quimioteràpia del càncer; Quimioterapia del cancer; Cancer chemotherapy; Conjugat polímer-medicament; Conjugado polímero-fármaco; Drug-polymer conjugate; Ciències de la Salut; 615

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APA (6th Edition):

Plà Solans, H. (2014). Design, synthesis and biological evaluation of new polymer-drug conjugates based on polyglutamic acid and 5-Fluorouracil for the treatment of advanced colorectal cancer. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/284644

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):

Plà Solans, Helena. “Design, synthesis and biological evaluation of new polymer-drug conjugates based on polyglutamic acid and 5-Fluorouracil for the treatment of advanced colorectal cancer.” 2014. Thesis, Universitat de Barcelona. Accessed June 20, 2019. http://hdl.handle.net/10803/284644.

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

MLA Handbook (7th Edition):

Plà Solans, Helena. “Design, synthesis and biological evaluation of new polymer-drug conjugates based on polyglutamic acid and 5-Fluorouracil for the treatment of advanced colorectal cancer.” 2014. Web. 20 Jun 2019.

Vancouver:

Plà Solans H. Design, synthesis and biological evaluation of new polymer-drug conjugates based on polyglutamic acid and 5-Fluorouracil for the treatment of advanced colorectal cancer. [Internet] [Thesis]. Universitat de Barcelona; 2014. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10803/284644.

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

Council of Science Editors:

Plà Solans H. Design, synthesis and biological evaluation of new polymer-drug conjugates based on polyglutamic acid and 5-Fluorouracil for the treatment of advanced colorectal cancer. [Thesis]. Universitat de Barcelona; 2014. Available from: http://hdl.handle.net/10803/284644

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

19. BAI JING. Biochemical and molecular characterisation of multidrug resistance protein 4 (MRP4).

Degree: 2003, National University of Singapore

Subjects/Keywords: multi-drug resistance protein; drug resistance; purine analogue; glutathione-S-conjugate; site-directed mutagenesis; substrate specificity

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APA (6th Edition):

JING, B. (2003). Biochemical and molecular characterisation of multidrug resistance protein 4 (MRP4). (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/17529

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):

JING, BAI. “Biochemical and molecular characterisation of multidrug resistance protein 4 (MRP4).” 2003. Thesis, National University of Singapore. Accessed June 20, 2019. http://scholarbank.nus.edu.sg/handle/10635/17529.

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

MLA Handbook (7th Edition):

JING, BAI. “Biochemical and molecular characterisation of multidrug resistance protein 4 (MRP4).” 2003. Web. 20 Jun 2019.

Vancouver:

JING B. Biochemical and molecular characterisation of multidrug resistance protein 4 (MRP4). [Internet] [Thesis]. National University of Singapore; 2003. [cited 2019 Jun 20]. Available from: http://scholarbank.nus.edu.sg/handle/10635/17529.

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

Council of Science Editors:

JING B. Biochemical and molecular characterisation of multidrug resistance protein 4 (MRP4). [Thesis]. National University of Singapore; 2003. Available from: http://scholarbank.nus.edu.sg/handle/10635/17529

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


Kyoto University / 京都大学

20. Shinmi, Daisuke. Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity : 薬学的活性を改善するための抗体および抗体技術に関する研究.

Degree: 博士(工学), 2018, Kyoto University / 京都大学

新制・論文博士

乙第13145号

論工博第4163号

Subjects/Keywords: antibody; antibody-drug conjugate; site-specific conjugation; carcinoembryonic antigen; TNF-related apoptosis-inducing ligand receptor 2

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APA (6th Edition):

Shinmi, D. (2018). Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity : 薬学的活性を改善するための抗体および抗体技術に関する研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/230980 ; http://dx.doi.org/10.14989/doctor.r13145

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):

Shinmi, Daisuke. “Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity : 薬学的活性を改善するための抗体および抗体技術に関する研究.” 2018. Thesis, Kyoto University / 京都大学. Accessed June 20, 2019. http://hdl.handle.net/2433/230980 ; http://dx.doi.org/10.14989/doctor.r13145.

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

MLA Handbook (7th Edition):

Shinmi, Daisuke. “Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity : 薬学的活性を改善するための抗体および抗体技術に関する研究.” 2018. Web. 20 Jun 2019.

Vancouver:

Shinmi D. Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity : 薬学的活性を改善するための抗体および抗体技術に関する研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2018. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2433/230980 ; http://dx.doi.org/10.14989/doctor.r13145.

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

Council of Science Editors:

Shinmi D. Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity : 薬学的活性を改善するための抗体および抗体技術に関する研究. [Thesis]. Kyoto University / 京都大学; 2018. Available from: http://hdl.handle.net/2433/230980 ; http://dx.doi.org/10.14989/doctor.r13145

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


Kyoto University

21. Shinmi, Daisuke. Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity .

Degree: 2018, Kyoto University

Subjects/Keywords: antibody; antibody-drug conjugate; site-specific conjugation; carcinoembryonic antigen; TNF-related apoptosis-inducing ligand receptor 2

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APA (6th Edition):

Shinmi, D. (2018). Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/230980

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):

Shinmi, Daisuke. “Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity .” 2018. Thesis, Kyoto University. Accessed June 20, 2019. http://hdl.handle.net/2433/230980.

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

MLA Handbook (7th Edition):

Shinmi, Daisuke. “Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity .” 2018. Web. 20 Jun 2019.

Vancouver:

Shinmi D. Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity . [Internet] [Thesis]. Kyoto University; 2018. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2433/230980.

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

Council of Science Editors:

Shinmi D. Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity . [Thesis]. Kyoto University; 2018. Available from: http://hdl.handle.net/2433/230980

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


KTH

22. Heckscher, Hans. Monoklonala antrikroppar - en översiktsstudie.

Degree: Biotechnology (BIO), 2016, KTH

Subjects/Keywords: Monoclonal antibody; IgG; Antibody-drug conjugate; cancer; Medicine; monoklonala antikroppar; Engineering and Technology; Teknik och teknologier

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APA (6th Edition):

Heckscher, H. (2016). Monoklonala antrikroppar - en översiktsstudie. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-207179

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):

Heckscher, Hans. “Monoklonala antrikroppar - en översiktsstudie.” 2016. Thesis, KTH. Accessed June 20, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-207179.

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

MLA Handbook (7th Edition):

Heckscher, Hans. “Monoklonala antrikroppar - en översiktsstudie.” 2016. Web. 20 Jun 2019.

Vancouver:

Heckscher H. Monoklonala antrikroppar - en översiktsstudie. [Internet] [Thesis]. KTH; 2016. [cited 2019 Jun 20]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-207179.

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

Council of Science Editors:

Heckscher H. Monoklonala antrikroppar - en översiktsstudie. [Thesis]. KTH; 2016. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-207179

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


Université de Montréal

23. Melkoumov, Alexandre. Conception d'espaceurs pour relever les défis de bioconjugaison .

Degree: 2019, Université de Montréal

Subjects/Keywords: Espaceur; Conjugaison; Bioconjugués; GM1; CTB; Perméabilité; Biodisponibilité orale; Anticorps conjugué à un médicament (ADC); Spacer; Conjugation; Bioconjugates; Permeability; Oral bioavailability; Antibody drug conjugate

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APA (6th Edition):

Melkoumov, A. (2019). Conception d'espaceurs pour relever les défis de bioconjugaison . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/21824

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):

Melkoumov, Alexandre. “Conception d'espaceurs pour relever les défis de bioconjugaison .” 2019. Thesis, Université de Montréal. Accessed June 20, 2019. http://hdl.handle.net/1866/21824.

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

MLA Handbook (7th Edition):

Melkoumov, Alexandre. “Conception d'espaceurs pour relever les défis de bioconjugaison .” 2019. Web. 20 Jun 2019.

Vancouver:

Melkoumov A. Conception d'espaceurs pour relever les défis de bioconjugaison . [Internet] [Thesis]. Université de Montréal; 2019. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1866/21824.

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

Council of Science Editors:

Melkoumov A. Conception d'espaceurs pour relever les défis de bioconjugaison . [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/21824

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

24. Kuruvilla, Sibu. Development of Targeted, Enzyme-Activated Nano-Conjugates for Hepatic Cancer Therapy.

Degree: PhD, Materials Science and Engineering, 2017, University of Michigan

 Hepatocellular carcinoma (HCC) is the 5th most commonly-occurring cancer worldwide and the 2nd highest cause for cancer-related deaths globally. The current treatment strategy is the… (more)

Subjects/Keywords: Nano-conjugates for hepatic cancer therapy; dendrimer; N-acetylgalactosamine; doxorubicin; enzyme-activated drug linkage; 2nd generation antibody-drug conjugate; Biomedical Engineering; Materials Science and Engineering; Science (General); Statistics and Numeric Data; Engineering; Science

…Co-loaded nano-conjugate strategy 157 216 218 219 220 Appendix Figures A1. Compound 11… …Compound 11 1H NMR C10. 1H NMR of conjugate 12 C11. 1H NMR of conjugate 12 (expansion 1)… …C12. 1H NMR of conjugate 12 (expansion 2) C13. 1H NMR of conjugate 12 (… …expansion 3) C14. MALDI of conjugate 12 C15. 1H NMR of conjugate 13 C16. 1H NMR of conjugate… …14 C17. 1H NMR of conjugate 15 C18. 1H NMR of conjugate 16 C19. 1H NMR of conjugate 17 C20… 

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APA (6th Edition):

Kuruvilla, S. (2017). Development of Targeted, Enzyme-Activated Nano-Conjugates for Hepatic Cancer Therapy. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/136952

Chicago Manual of Style (16th Edition):

Kuruvilla, Sibu. “Development of Targeted, Enzyme-Activated Nano-Conjugates for Hepatic Cancer Therapy.” 2017. Doctoral Dissertation, University of Michigan. Accessed June 20, 2019. http://hdl.handle.net/2027.42/136952.

MLA Handbook (7th Edition):

Kuruvilla, Sibu. “Development of Targeted, Enzyme-Activated Nano-Conjugates for Hepatic Cancer Therapy.” 2017. Web. 20 Jun 2019.

Vancouver:

Kuruvilla S. Development of Targeted, Enzyme-Activated Nano-Conjugates for Hepatic Cancer Therapy. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2027.42/136952.

Council of Science Editors:

Kuruvilla S. Development of Targeted, Enzyme-Activated Nano-Conjugates for Hepatic Cancer Therapy. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/136952

25. Kirejev, Vladimir. Exploring nanosystems for biomedical applications focusing on photodynamic therapy and drug delivery.

Degree: 2014, University of Gothenburg / Göteborgs Universitet

 The increasing incidences of cancer and related deaths call for the development of new and improved treatment modalities. Photodynamic therapy (PDT) today is an alternative… (more)

Subjects/Keywords: Photodynamic therapy; PDT enhancement; Nitric oxide; NO-based PDT; Targeted drug delivery; Galectin-3; mTHPP; Cyclodextrin; CD-mTHPP conjugate; PpIX AuNP combination; Two-photon microscopy; FLIM; Cell phototoxicity; Ex vivo skin

Page 1 Page 2

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APA (6th Edition):

Kirejev, V. (2014). Exploring nanosystems for biomedical applications focusing on photodynamic therapy and drug delivery. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/35177

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):

Kirejev, Vladimir. “Exploring nanosystems for biomedical applications focusing on photodynamic therapy and drug delivery.” 2014. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed June 20, 2019. http://hdl.handle.net/2077/35177.

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

MLA Handbook (7th Edition):

Kirejev, Vladimir. “Exploring nanosystems for biomedical applications focusing on photodynamic therapy and drug delivery.” 2014. Web. 20 Jun 2019.

Vancouver:

Kirejev V. Exploring nanosystems for biomedical applications focusing on photodynamic therapy and drug delivery. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2014. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/2077/35177.

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

Council of Science Editors:

Kirejev V. Exploring nanosystems for biomedical applications focusing on photodynamic therapy and drug delivery. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2014. Available from: http://hdl.handle.net/2077/35177

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

.