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You searched for subject:(Antithrombotique Antibody Drug Conjugate). Showing records 1 – 30 of 12257 total matches.

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1. Kizlik-Masson, Claire. Anticorps anti-FP4/héparine et protéases : nouvelles stratégies thérapeutiques dans les thrombopénies induites par l'héparine : Anti-PF4/heparin antibodies and proteasis : new therapeutic strategies for heparin-induced thrombocytopenia.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Université François-Rabelais de Tours

Les Thrombopénies Induites par l’Héparine (TIH) sont une complication sévère des traitements par l’héparine dues à des IgG qui ciblent le facteur plaquettaire 4 modifié… (more)

Subjects/Keywords: Thrombopénie induite par l’Héparine; FcγR; Anticorps; Protéases; IdeS; Antithrombotique Antibody- Drug Conjugate; Heparin-Induced Thrombocytopenia; FcγR; Antibody; Proteases; IdeS; Antithrombotic Antibody- Drug Conjugate (ADC)

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

APA (6th Edition):

Kizlik-Masson, C. (2018). Anticorps anti-FP4/héparine et protéases : nouvelles stratégies thérapeutiques dans les thrombopénies induites par l'héparine : Anti-PF4/heparin antibodies and proteasis : new therapeutic strategies for heparin-induced thrombocytopenia. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2018TOUR3313

Chicago Manual of Style (16th Edition):

Kizlik-Masson, Claire. “Anticorps anti-FP4/héparine et protéases : nouvelles stratégies thérapeutiques dans les thrombopénies induites par l'héparine : Anti-PF4/heparin antibodies and proteasis : new therapeutic strategies for heparin-induced thrombocytopenia.” 2018. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed October 20, 2019. http://www.theses.fr/2018TOUR3313.

MLA Handbook (7th Edition):

Kizlik-Masson, Claire. “Anticorps anti-FP4/héparine et protéases : nouvelles stratégies thérapeutiques dans les thrombopénies induites par l'héparine : Anti-PF4/heparin antibodies and proteasis : new therapeutic strategies for heparin-induced thrombocytopenia.” 2018. Web. 20 Oct 2019.

Vancouver:

Kizlik-Masson C. Anticorps anti-FP4/héparine et protéases : nouvelles stratégies thérapeutiques dans les thrombopénies induites par l'héparine : Anti-PF4/heparin antibodies and proteasis : new therapeutic strategies for heparin-induced thrombocytopenia. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2018. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2018TOUR3313.

Council of Science Editors:

Kizlik-Masson C. Anticorps anti-FP4/héparine et protéases : nouvelles stratégies thérapeutiques dans les thrombopénies induites par l'héparine : Anti-PF4/heparin antibodies and proteasis : new therapeutic strategies for heparin-induced thrombocytopenia. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2018. Available from: http://www.theses.fr/2018TOUR3313


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 October 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 Oct 2019.

Vancouver:

Vanner S. Anticancer Natural Products: Evolution and their Biosynthetic Site-Selective Conjugation to Antibodies. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2019 Oct 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 Waterloo

3. 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 October 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 Oct 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 Oct 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


University of Arizona

4. Coyle, Kelsey Rebecca. Development of an Anti-Muc1 Antibody-Drug Conjugate with Specificity to Target Cancer .

Degree: 2019, University of Arizona

 Ever since Paul Ehrlich, Nobel Prize winner and the founder of chemotherapy, postulated that “magic bullets” can be created and used to fight human disease,… (more)

Subjects/Keywords: Antibody; Antibody-Drug Conjugate; Anti-Muc1; Cancer; Muc1; Mucin 1

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APA (6th Edition):

Coyle, K. R. (2019). Development of an Anti-Muc1 Antibody-Drug Conjugate with Specificity to Target Cancer . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/633100

Chicago Manual of Style (16th Edition):

Coyle, Kelsey Rebecca. “Development of an Anti-Muc1 Antibody-Drug Conjugate with Specificity to Target Cancer .” 2019. Masters Thesis, University of Arizona. Accessed October 20, 2019. http://hdl.handle.net/10150/633100.

MLA Handbook (7th Edition):

Coyle, Kelsey Rebecca. “Development of an Anti-Muc1 Antibody-Drug Conjugate with Specificity to Target Cancer .” 2019. Web. 20 Oct 2019.

Vancouver:

Coyle KR. Development of an Anti-Muc1 Antibody-Drug Conjugate with Specificity to Target Cancer . [Internet] [Masters thesis]. University of Arizona; 2019. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10150/633100.

Council of Science Editors:

Coyle KR. Development of an Anti-Muc1 Antibody-Drug Conjugate with Specificity to Target Cancer . [Masters Thesis]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/633100


University of Kansas

5. Knewtson, Kelsey Erin. Studies of novel targeted drug delivery systems and molecular probes of cancer biology.

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

 Cancer is a complex family of diseases. As our understanding of cancer biology has improved, so has our ability to treat the pathology associated with… (more)

Subjects/Keywords: Chemistry; Biology; antibody drug conjugate; endosome disruption; fluorescence; peroxynitrite

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APA (6th Edition):

Knewtson, K. E. (2019). Studies of novel targeted drug delivery systems and molecular probes of cancer biology. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/29547

Chicago Manual of Style (16th Edition):

Knewtson, Kelsey Erin. “Studies of novel targeted drug delivery systems and molecular probes of cancer biology.” 2019. Doctoral Dissertation, University of Kansas. Accessed October 20, 2019. http://hdl.handle.net/1808/29547.

MLA Handbook (7th Edition):

Knewtson, Kelsey Erin. “Studies of novel targeted drug delivery systems and molecular probes of cancer biology.” 2019. Web. 20 Oct 2019.

Vancouver:

Knewtson KE. Studies of novel targeted drug delivery systems and molecular probes of cancer biology. [Internet] [Doctoral dissertation]. University of Kansas; 2019. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1808/29547.

Council of Science Editors:

Knewtson KE. Studies of novel targeted drug delivery systems and molecular probes of cancer biology. [Doctoral Dissertation]. University of Kansas; 2019. Available from: http://hdl.handle.net/1808/29547


University of Michigan

6. 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 October 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 Oct 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 Oct 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


Uppsala University

7. 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 October 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 Oct 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 Oct 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 Lund

8. 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 October 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 Oct 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 Oct 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

9. 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 October 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 Oct 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 Oct 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


University of Michigan

10. Tian, Yuwei. Developing Structural Mass Spectrometry Approaches for Therapeutic Antibody Characterization.

Degree: PhD, Chemistry, 2018, University of Michigan

 Therapeutic monoclonal antibodies (mAbs) and mAb-based therapeutics represent the fastest growing class of biopharmaceuticals over the past few decades. In comparison with the small molecule… (more)

Subjects/Keywords: Ion Mobility-Mass Spectrometry; Collision Induced Unfolding; Biopharmaceuticals; Therapeutic Antibodies; Antibody-Drug Conjugate; HDX-MS; Chemistry; Science

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APA (6th Edition):

Tian, Y. (2018). Developing Structural Mass Spectrometry Approaches for Therapeutic Antibody Characterization. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/146086

Chicago Manual of Style (16th Edition):

Tian, Yuwei. “Developing Structural Mass Spectrometry Approaches for Therapeutic Antibody Characterization.” 2018. Doctoral Dissertation, University of Michigan. Accessed October 20, 2019. http://hdl.handle.net/2027.42/146086.

MLA Handbook (7th Edition):

Tian, Yuwei. “Developing Structural Mass Spectrometry Approaches for Therapeutic Antibody Characterization.” 2018. Web. 20 Oct 2019.

Vancouver:

Tian Y. Developing Structural Mass Spectrometry Approaches for Therapeutic Antibody Characterization. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2027.42/146086.

Council of Science Editors:

Tian Y. Developing Structural Mass Spectrometry Approaches for Therapeutic Antibody Characterization. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/146086


University of Oxford

11. 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 October 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 Oct 2019.

Vancouver:

Yamamoto K. Modification and application of glycosidases to create homogeneous glycoconjugates. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Oct 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

12. 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 (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 October 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 Oct 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 Oct 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.


Kyoto University / 京都大学

13. 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 October 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 Oct 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 Oct 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

14. 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 October 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 Oct 2019.

Vancouver:

Shinmi D. Characterization of the antibodies and antibody technologies to improve the pharmaceutical activity . [Internet] [Thesis]. Kyoto University; 2018. [cited 2019 Oct 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

15. 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 October 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 Oct 2019.

Vancouver:

Heckscher H. Monoklonala antrikroppar - en översiktsstudie. [Internet] [Thesis]. KTH; 2016. [cited 2019 Oct 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

16. Jahani, Zeena. Performance Improvement and Outcome Monitoring of the Quick Screen Urinalysis Drug Test .

Degree: 2014, California State University – San Marcos

 This Semester-in-Residence project was conducted at Syntron Bioresearch, Inc. located in Carlsbad, California. Syntron Bioresearch is a research manufacturing company specializing in rapid in vitro… (more)

Subjects/Keywords: Membrane; Antibody; Drug Test

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APA (6th Edition):

Jahani, Z. (2014). Performance Improvement and Outcome Monitoring of the Quick Screen Urinalysis Drug Test . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.3/124689

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):

Jahani, Zeena. “Performance Improvement and Outcome Monitoring of the Quick Screen Urinalysis Drug Test .” 2014. Thesis, California State University – San Marcos. Accessed October 20, 2019. http://hdl.handle.net/10211.3/124689.

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

MLA Handbook (7th Edition):

Jahani, Zeena. “Performance Improvement and Outcome Monitoring of the Quick Screen Urinalysis Drug Test .” 2014. Web. 20 Oct 2019.

Vancouver:

Jahani Z. Performance Improvement and Outcome Monitoring of the Quick Screen Urinalysis Drug Test . [Internet] [Thesis]. California State University – San Marcos; 2014. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10211.3/124689.

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

Council of Science Editors:

Jahani Z. Performance Improvement and Outcome Monitoring of the Quick Screen Urinalysis Drug Test . [Thesis]. California State University – San Marcos; 2014. Available from: http://hdl.handle.net/10211.3/124689

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


University of Notre Dame

17. 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 October 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 Oct 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 Oct 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

18. 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 October 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 Oct 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 Oct 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


University of Melbourne

19. KOSTENKO, LYUDMILA. Development of a diagnostic test for the prediction and prevention of HLA-B57/B58-linked drug hypersensitivities.

Degree: 2014, University of Melbourne

 HLA-B*57:01 is strongly associated with a life-threatening hypersensitivity to the HIV drug abacavir, liver toxicity from the antibiotic flucloxacillin and is a marker for the… (more)

Subjects/Keywords: drug hypersensitivity; human leukocyte antigen; monoclonal antibody

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APA (6th Edition):

KOSTENKO, L. (2014). Development of a diagnostic test for the prediction and prevention of HLA-B57/B58-linked drug hypersensitivities. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/51134

Chicago Manual of Style (16th Edition):

KOSTENKO, LYUDMILA. “Development of a diagnostic test for the prediction and prevention of HLA-B57/B58-linked drug hypersensitivities.” 2014. Masters Thesis, University of Melbourne. Accessed October 20, 2019. http://hdl.handle.net/11343/51134.

MLA Handbook (7th Edition):

KOSTENKO, LYUDMILA. “Development of a diagnostic test for the prediction and prevention of HLA-B57/B58-linked drug hypersensitivities.” 2014. Web. 20 Oct 2019.

Vancouver:

KOSTENKO L. Development of a diagnostic test for the prediction and prevention of HLA-B57/B58-linked drug hypersensitivities. [Internet] [Masters thesis]. University of Melbourne; 2014. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/11343/51134.

Council of Science Editors:

KOSTENKO L. Development of a diagnostic test for the prediction and prevention of HLA-B57/B58-linked drug hypersensitivities. [Masters Thesis]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/51134


Northeastern University

20. Gedeon, Nicholas. Technology-mediated functionalization of proteins and antibodies using a continuous flow microreactor.

Degree: MS, Department of Chemistry and Chemical Biology, 2015, Northeastern University

 The therapeutic index of conventional chemotherapeutic techniques is narrow and treatment results in a variety of systemic issues. Antibody-drug conjugates represent a targeted delivery method… (more)

Subjects/Keywords: antibody; antibody-drug conjugation; continuous flow; drug-to-antibody ratio; protein functionalization; Antibody-drug conjugates; Antineoplastic antibiotics; Immunoglobulins; Proteins; Cell surface antigens; Drug targeting; Microreactors; Infliximab

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APA (6th Edition):

Gedeon, N. (2015). Technology-mediated functionalization of proteins and antibodies using a continuous flow microreactor. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20193646

Chicago Manual of Style (16th Edition):

Gedeon, Nicholas. “Technology-mediated functionalization of proteins and antibodies using a continuous flow microreactor.” 2015. Masters Thesis, Northeastern University. Accessed October 20, 2019. http://hdl.handle.net/2047/D20193646.

MLA Handbook (7th Edition):

Gedeon, Nicholas. “Technology-mediated functionalization of proteins and antibodies using a continuous flow microreactor.” 2015. Web. 20 Oct 2019.

Vancouver:

Gedeon N. Technology-mediated functionalization of proteins and antibodies using a continuous flow microreactor. [Internet] [Masters thesis]. Northeastern University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2047/D20193646.

Council of Science Editors:

Gedeon N. Technology-mediated functionalization of proteins and antibodies using a continuous flow microreactor. [Masters Thesis]. Northeastern University; 2015. Available from: http://hdl.handle.net/2047/D20193646

21. Sivado, Eva. New bacterial transglutaminase Q-tag substrate for the development of site-specific Antibody Drug Conjugates : Nouveaux subtrats Q-tag pour le développement d’ADCs site spécifique par activité enzymatique transglutaminase.

Degree: Docteur es, Immunologie, 2018, Lyon

Es ADCs (Antibody-Drug Conjugates) correspondent à une nouvelle stratégie thérapeutique anti-tumorale particulièrement prometteuse. Néanmoins, les ADCs actuellement utilisés en clinique sont obtenus par conjugaisons chimiques,… (more)

Subjects/Keywords: Antibody-Drug Conjugates; Couplage site-spécifique; Transglutaminase; Fragments d’anticorps; Antibody-drug conjugates; Site-specific conjugation; Microbial transglutaminase; Antibody fragments; 570

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APA (6th Edition):

Sivado, E. (2018). New bacterial transglutaminase Q-tag substrate for the development of site-specific Antibody Drug Conjugates : Nouveaux subtrats Q-tag pour le développement d’ADCs site spécifique par activité enzymatique transglutaminase. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2018LYSE1261

Chicago Manual of Style (16th Edition):

Sivado, Eva. “New bacterial transglutaminase Q-tag substrate for the development of site-specific Antibody Drug Conjugates : Nouveaux subtrats Q-tag pour le développement d’ADCs site spécifique par activité enzymatique transglutaminase.” 2018. Doctoral Dissertation, Lyon. Accessed October 20, 2019. http://www.theses.fr/2018LYSE1261.

MLA Handbook (7th Edition):

Sivado, Eva. “New bacterial transglutaminase Q-tag substrate for the development of site-specific Antibody Drug Conjugates : Nouveaux subtrats Q-tag pour le développement d’ADCs site spécifique par activité enzymatique transglutaminase.” 2018. Web. 20 Oct 2019.

Vancouver:

Sivado E. New bacterial transglutaminase Q-tag substrate for the development of site-specific Antibody Drug Conjugates : Nouveaux subtrats Q-tag pour le développement d’ADCs site spécifique par activité enzymatique transglutaminase. [Internet] [Doctoral dissertation]. Lyon; 2018. [cited 2019 Oct 20]. Available from: http://www.theses.fr/2018LYSE1261.

Council of Science Editors:

Sivado E. New bacterial transglutaminase Q-tag substrate for the development of site-specific Antibody Drug Conjugates : Nouveaux subtrats Q-tag pour le développement d’ADCs site spécifique par activité enzymatique transglutaminase. [Doctoral Dissertation]. Lyon; 2018. Available from: http://www.theses.fr/2018LYSE1261


Université de Montréal

22. 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 October 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 Oct 2019.

Vancouver:

Melkoumov A. Conception d'espaceurs pour relever les défis de bioconjugaison . [Internet] [Thesis]. Université de Montréal; 2019. [cited 2019 Oct 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


Université Catholique de Louvain

23. 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 October 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 Oct 2019.

Vancouver:

Luo T. PEGylation of paclitaxel for inhaled chemotherapy. [Internet] [Thesis]. Université Catholique de Louvain; 2016. [cited 2019 Oct 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

24. [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 October 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 Oct 2019.

Vancouver:

author] [. The Evolution of Phosphoramidates from Small-Molecule Inhibitors to Tunable Cleavable Linkers . [Internet] [Thesis]. Washington State University; 2016. [cited 2019 Oct 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

25. 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 October 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 Oct 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 Oct 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

26. Costa, Isabel de Camargo. Avaliação da resposta humoral à vacina pneumocócica conjugada 7-valente em grupo de crianças com infecção pelo HIV.

Degree: Mestrado, Pediatria, 2007, University of São Paulo

A doença pneumocócica invasiva é importante causa de morbi-mortalidade em crianças infectadas pelo HIV. A vacina pneumocócica conjugada 7-valente já teve sua segurança, eficácia e… (more)

Subjects/Keywords: Antibody formation; Child; Criança; Formação de anticorpos; HIV infections; Infecções pelo HIV; Streptococcus pneumoniae; Streptococcus pneumoniae; Vaccines conjugate; Vacinas conjugadas

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APA (6th Edition):

Costa, I. d. C. (2007). Avaliação da resposta humoral à vacina pneumocócica conjugada 7-valente em grupo de crianças com infecção pelo HIV. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5141/tde-11122007-124435/ ;

Chicago Manual of Style (16th Edition):

Costa, Isabel de Camargo. “Avaliação da resposta humoral à vacina pneumocócica conjugada 7-valente em grupo de crianças com infecção pelo HIV.” 2007. Masters Thesis, University of São Paulo. Accessed October 20, 2019. http://www.teses.usp.br/teses/disponiveis/5/5141/tde-11122007-124435/ ;.

MLA Handbook (7th Edition):

Costa, Isabel de Camargo. “Avaliação da resposta humoral à vacina pneumocócica conjugada 7-valente em grupo de crianças com infecção pelo HIV.” 2007. Web. 20 Oct 2019.

Vancouver:

Costa IdC. Avaliação da resposta humoral à vacina pneumocócica conjugada 7-valente em grupo de crianças com infecção pelo HIV. [Internet] [Masters thesis]. University of São Paulo; 2007. [cited 2019 Oct 20]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-11122007-124435/ ;.

Council of Science Editors:

Costa IdC. Avaliação da resposta humoral à vacina pneumocócica conjugada 7-valente em grupo de crianças com infecção pelo HIV. [Masters Thesis]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/5/5141/tde-11122007-124435/ ;


University of Toledo Health Science Campus

27. Ohtola, Jennifer A. Pneumococcal Vaccination in Aging HIV-Infected Individuals.

Degree: PhD, Biomedical Sciences (Infection, Immunity, and Transplantation), 2015, University of Toledo Health Science Campus

 Advanced age and human immunodeficiency virus (HIV) infection are both risk factors for <i>Streptococcus pneumoniae</i> infections due to immunological dysfunction. The aging HIV-infected (HIV+) population… (more)

Subjects/Keywords: Immunology; Microbiology; Streptococcus pneumoniae; pneumococcal conjugate vaccine; pneumococcal polysaccharide vaccine; HIV infection; aging; B cells; antibody

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APA (6th Edition):

Ohtola, J. A. (2015). Pneumococcal Vaccination in Aging HIV-Infected Individuals. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1435076215

Chicago Manual of Style (16th Edition):

Ohtola, Jennifer A. “Pneumococcal Vaccination in Aging HIV-Infected Individuals.” 2015. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed October 20, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=mco1435076215.

MLA Handbook (7th Edition):

Ohtola, Jennifer A. “Pneumococcal Vaccination in Aging HIV-Infected Individuals.” 2015. Web. 20 Oct 2019.

Vancouver:

Ohtola JA. Pneumococcal Vaccination in Aging HIV-Infected Individuals. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2015. [cited 2019 Oct 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1435076215.

Council of Science Editors:

Ohtola JA. Pneumococcal Vaccination in Aging HIV-Infected Individuals. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1435076215


University of Pennsylvania

28. Warden-Rothman, Robert Leslie. The Development, Use, and Optimization of Sortase-Tag Expressed Protein Ligation.

Degree: 2015, University of Pennsylvania

 Molecular imaging is an emerging field that seeks to combine the mechanistic detail of biochemical assays with the the broad phenotypic data obtained from non-invasive… (more)

Subjects/Keywords: antibody drug conjugates; bioconjugation; contrast agents; molecular imaging; sortase; Biochemistry; Biomedical

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APA (6th Edition):

Warden-Rothman, R. L. (2015). The Development, Use, and Optimization of Sortase-Tag Expressed Protein Ligation. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1160

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):

Warden-Rothman, Robert Leslie. “The Development, Use, and Optimization of Sortase-Tag Expressed Protein Ligation.” 2015. Thesis, University of Pennsylvania. Accessed October 20, 2019. https://repository.upenn.edu/edissertations/1160.

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

MLA Handbook (7th Edition):

Warden-Rothman, Robert Leslie. “The Development, Use, and Optimization of Sortase-Tag Expressed Protein Ligation.” 2015. Web. 20 Oct 2019.

Vancouver:

Warden-Rothman RL. The Development, Use, and Optimization of Sortase-Tag Expressed Protein Ligation. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2019 Oct 20]. Available from: https://repository.upenn.edu/edissertations/1160.

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

Council of Science Editors:

Warden-Rothman RL. The Development, Use, and Optimization of Sortase-Tag Expressed Protein Ligation. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1160

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


University of Pennsylvania

29. Bagchi, Atrish. Mechanisms of Extracellular Oncogenic Dysregulation and Antibody Targeting of the Epidermal Growth Factor Receptor.

Degree: 2016, University of Pennsylvania

 Regulation of the Epidermal Growth Factor Receptor (EGFR) by its growth factor ligands is critical in many biological processes, including development and tissue maintenance and… (more)

Subjects/Keywords: antibody; cancer; drug; EGFR; oncogenic mutation; resistance; Biochemistry; Biophysics

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APA (6th Edition):

Bagchi, A. (2016). Mechanisms of Extracellular Oncogenic Dysregulation and Antibody Targeting of the Epidermal Growth Factor Receptor. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1596

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):

Bagchi, Atrish. “Mechanisms of Extracellular Oncogenic Dysregulation and Antibody Targeting of the Epidermal Growth Factor Receptor.” 2016. Thesis, University of Pennsylvania. Accessed October 20, 2019. https://repository.upenn.edu/edissertations/1596.

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

MLA Handbook (7th Edition):

Bagchi, Atrish. “Mechanisms of Extracellular Oncogenic Dysregulation and Antibody Targeting of the Epidermal Growth Factor Receptor.” 2016. Web. 20 Oct 2019.

Vancouver:

Bagchi A. Mechanisms of Extracellular Oncogenic Dysregulation and Antibody Targeting of the Epidermal Growth Factor Receptor. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2019 Oct 20]. Available from: https://repository.upenn.edu/edissertations/1596.

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

Council of Science Editors:

Bagchi A. Mechanisms of Extracellular Oncogenic Dysregulation and Antibody Targeting of the Epidermal Growth Factor Receptor. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/1596

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


Northeastern University

30. Fallano, Meaghan M. Continuous flow chemistry: applications in chemistry education and bioconjugation.

Degree: PhD, Department of Chemistry and Chemical Biology, 2017, Northeastern University

 Applications of continuous flow chemistry have increased significantly over the past two decades, owing much success to adoption of the new methodology in both academic… (more)

Subjects/Keywords: continuous flow chemistry; antibody-drug conjugates; azides; triazoles

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APA (6th Edition):

Fallano, M. M. (2017). Continuous flow chemistry: applications in chemistry education and bioconjugation. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20248781

Chicago Manual of Style (16th Edition):

Fallano, Meaghan M. “Continuous flow chemistry: applications in chemistry education and bioconjugation.” 2017. Doctoral Dissertation, Northeastern University. Accessed October 20, 2019. http://hdl.handle.net/2047/D20248781.

MLA Handbook (7th Edition):

Fallano, Meaghan M. “Continuous flow chemistry: applications in chemistry education and bioconjugation.” 2017. Web. 20 Oct 2019.

Vancouver:

Fallano MM. Continuous flow chemistry: applications in chemistry education and bioconjugation. [Internet] [Doctoral dissertation]. Northeastern University; 2017. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/2047/D20248781.

Council of Science Editors:

Fallano MM. Continuous flow chemistry: applications in chemistry education and bioconjugation. [Doctoral Dissertation]. Northeastern University; 2017. Available from: http://hdl.handle.net/2047/D20248781

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