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You searched for subject:( monoclonal antibody). Showing records 1 – 30 of 247 total matches.

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University of Debrecen

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

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

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

Subjects/Keywords: monoclonal antibody

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Baba Adamu, Harira. “Monoclonal antibodies in the treatment of colorectal cancer .” Thesis, University of Debrecen. Accessed October 19, 2019. http://hdl.handle.net/2437/218612.

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

MLA Handbook (7th Edition):

Baba Adamu, Harira. “Monoclonal antibodies in the treatment of colorectal cancer .” Web. 19 Oct 2019.

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

Vancouver:

Baba Adamu H. Monoclonal antibodies in the treatment of colorectal cancer . [Internet] [Thesis]. University of Debrecen; [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2437/218612.

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

Council of Science Editors:

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

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


Colorado State University

2. Ishii, Toru. Development and application of new diagnostic assays for the detection of prion proteins in transmissible spongiform encephalopathies.

Degree: PhD, Cell and Molecular Biology, 2018, Colorado State University

 Transmissible spongiform encephalopathies (TSEs), well known as prion diseases, are fatal neurodegenerative disorders in humans and animals, which a prion protein (PrP) mainly implicates with… (more)

Subjects/Keywords: Glyocosylation; Prion; Monoclonal antibody; ELISA

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APA (6th Edition):

Ishii, T. (2018). Development and application of new diagnostic assays for the detection of prion proteins in transmissible spongiform encephalopathies. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/191285

Chicago Manual of Style (16th Edition):

Ishii, Toru. “Development and application of new diagnostic assays for the detection of prion proteins in transmissible spongiform encephalopathies.” 2018. Doctoral Dissertation, Colorado State University. Accessed October 19, 2019. http://hdl.handle.net/10217/191285.

MLA Handbook (7th Edition):

Ishii, Toru. “Development and application of new diagnostic assays for the detection of prion proteins in transmissible spongiform encephalopathies.” 2018. Web. 19 Oct 2019.

Vancouver:

Ishii T. Development and application of new diagnostic assays for the detection of prion proteins in transmissible spongiform encephalopathies. [Internet] [Doctoral dissertation]. Colorado State University; 2018. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10217/191285.

Council of Science Editors:

Ishii T. Development and application of new diagnostic assays for the detection of prion proteins in transmissible spongiform encephalopathies. [Doctoral Dissertation]. Colorado State University; 2018. Available from: http://hdl.handle.net/10217/191285


University of Alberta

3. Ramji, Qahir A. Co-transplantation of neonatal porcine islets with Sertoli cells combined with short-term monoclonal antibody therapy in preventing neonatal porcine islet xenograft rejection.

Degree: MS, Department of Surgery, 2009, University of Alberta

 The need for an unlimited source of islets and a safer method of immunosuppression has limited the widespread application of islet transplantation. To remedy the… (more)

Subjects/Keywords: Anti-CD154 monoclonal antibody; Sertoli cells; Neonatal porcine islets; Anti-LFA-1 monoclonal antibody; Islet xenotransplantation; Anti-CD45RB monoclonal antibody

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APA (6th Edition):

Ramji, Q. A. (2009). Co-transplantation of neonatal porcine islets with Sertoli cells combined with short-term monoclonal antibody therapy in preventing neonatal porcine islet xenograft rejection. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/8336h2645

Chicago Manual of Style (16th Edition):

Ramji, Qahir A. “Co-transplantation of neonatal porcine islets with Sertoli cells combined with short-term monoclonal antibody therapy in preventing neonatal porcine islet xenograft rejection.” 2009. Masters Thesis, University of Alberta. Accessed October 19, 2019. https://era.library.ualberta.ca/files/8336h2645.

MLA Handbook (7th Edition):

Ramji, Qahir A. “Co-transplantation of neonatal porcine islets with Sertoli cells combined with short-term monoclonal antibody therapy in preventing neonatal porcine islet xenograft rejection.” 2009. Web. 19 Oct 2019.

Vancouver:

Ramji QA. Co-transplantation of neonatal porcine islets with Sertoli cells combined with short-term monoclonal antibody therapy in preventing neonatal porcine islet xenograft rejection. [Internet] [Masters thesis]. University of Alberta; 2009. [cited 2019 Oct 19]. Available from: https://era.library.ualberta.ca/files/8336h2645.

Council of Science Editors:

Ramji QA. Co-transplantation of neonatal porcine islets with Sertoli cells combined with short-term monoclonal antibody therapy in preventing neonatal porcine islet xenograft rejection. [Masters Thesis]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/8336h2645


University of Southern California

4. Guo, Jiacong. Design, synthesis and validation of Axl-targeted monoclonal antibody probe for microPET imaging of human lung cancer.

Degree: MS, Molecular Microbiology and Immunology, 2013, University of Southern California

 Accumulating experimental evidence indicates that overexpression of oncogenic receptor tyrosine kinase, Axl, plays a key role in the tumorigenesis and metastasis of various types of… (more)

Subjects/Keywords: Axl; monoclonal antibody; microPET imaging; lung cancer

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APA (6th Edition):

Guo, J. (2013). Design, synthesis and validation of Axl-targeted monoclonal antibody probe for microPET imaging of human lung cancer. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249951/rec/1873

Chicago Manual of Style (16th Edition):

Guo, Jiacong. “Design, synthesis and validation of Axl-targeted monoclonal antibody probe for microPET imaging of human lung cancer.” 2013. Masters Thesis, University of Southern California. Accessed October 19, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249951/rec/1873.

MLA Handbook (7th Edition):

Guo, Jiacong. “Design, synthesis and validation of Axl-targeted monoclonal antibody probe for microPET imaging of human lung cancer.” 2013. Web. 19 Oct 2019.

Vancouver:

Guo J. Design, synthesis and validation of Axl-targeted monoclonal antibody probe for microPET imaging of human lung cancer. [Internet] [Masters thesis]. University of Southern California; 2013. [cited 2019 Oct 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249951/rec/1873.

Council of Science Editors:

Guo J. Design, synthesis and validation of Axl-targeted monoclonal antibody probe for microPET imaging of human lung cancer. [Masters Thesis]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/249951/rec/1873


University of Melbourne

5. 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 19, 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. 19 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 19]. 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


University of Waterloo

6. Ho, Raymond. Proteomic Analysis of Chinese Hamster Ovary Cells Producing Glycosylated Monoclonal Antibodies.

Degree: 2013, University of Waterloo

 Therapeutic monoclonal antibodies (MAb) are produced as secreted complex glycoproteins from mammalian cell systems and represent one of the most important classes of therapeutic medicines… (more)

Subjects/Keywords: chinese hamster ovary; proteomic; glycosylation; monoclonal antibody

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APA (6th Edition):

Ho, R. (2013). Proteomic Analysis of Chinese Hamster Ovary Cells Producing Glycosylated Monoclonal Antibodies. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/7622

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):

Ho, Raymond. “Proteomic Analysis of Chinese Hamster Ovary Cells Producing Glycosylated Monoclonal Antibodies.” 2013. Thesis, University of Waterloo. Accessed October 19, 2019. http://hdl.handle.net/10012/7622.

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

MLA Handbook (7th Edition):

Ho, Raymond. “Proteomic Analysis of Chinese Hamster Ovary Cells Producing Glycosylated Monoclonal Antibodies.” 2013. Web. 19 Oct 2019.

Vancouver:

Ho R. Proteomic Analysis of Chinese Hamster Ovary Cells Producing Glycosylated Monoclonal Antibodies. [Internet] [Thesis]. University of Waterloo; 2013. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10012/7622.

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

Council of Science Editors:

Ho R. Proteomic Analysis of Chinese Hamster Ovary Cells Producing Glycosylated Monoclonal Antibodies. [Thesis]. University of Waterloo; 2013. Available from: http://hdl.handle.net/10012/7622

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


University of Debrecen

7. Bourara, Nor El Houda. A monoclonal antibody proteomics quest for conserved cognate epitopes between human and Drosophila melanogaster .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

Our aim from this work is to investigate the detectability of conserved epitopes detectable by BSI mAb-s in between human and Drosophila melanogaster using different methods. Advisors/Committee Members: Takács, László (advisor), Debreceni Egyetem::Általános Orvostudományi Kar (advisor).

Subjects/Keywords: BSI monoclonal antibody

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APA (6th Edition):

Bourara, N. E. H. (n.d.). A monoclonal antibody proteomics quest for conserved cognate epitopes between human and Drosophila melanogaster . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/255200

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):

Bourara, Nor El Houda. “A monoclonal antibody proteomics quest for conserved cognate epitopes between human and Drosophila melanogaster .” Thesis, University of Debrecen. Accessed October 19, 2019. http://hdl.handle.net/2437/255200.

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):

Bourara, Nor El Houda. “A monoclonal antibody proteomics quest for conserved cognate epitopes between human and Drosophila melanogaster .” Web. 19 Oct 2019.

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

Vancouver:

Bourara NEH. A monoclonal antibody proteomics quest for conserved cognate epitopes between human and Drosophila melanogaster . [Internet] [Thesis]. University of Debrecen; [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2437/255200.

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:

Bourara NEH. A monoclonal antibody proteomics quest for conserved cognate epitopes between human and Drosophila melanogaster . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/255200

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


University of Texas – Austin

8. Dinin, Aileen Kathryn. The manufacture and characterization of protein nanoclusters.

Degree: MSin Engineering, Chemical Engineering, 2013, University of Texas – Austin

 The ability to formulate monoclonal antibodies at high concentration in a low-viscosity form is of broad interest in drug delivery, as monoclonal antibody-based drugs are… (more)

Subjects/Keywords: Protein; Monoclonal antibody; Formulation; Excipient; Viscosity; Equilibrium

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APA (6th Edition):

Dinin, A. K. (2013). The manufacture and characterization of protein nanoclusters. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/27207

Chicago Manual of Style (16th Edition):

Dinin, Aileen Kathryn. “The manufacture and characterization of protein nanoclusters.” 2013. Masters Thesis, University of Texas – Austin. Accessed October 19, 2019. http://hdl.handle.net/2152/27207.

MLA Handbook (7th Edition):

Dinin, Aileen Kathryn. “The manufacture and characterization of protein nanoclusters.” 2013. Web. 19 Oct 2019.

Vancouver:

Dinin AK. The manufacture and characterization of protein nanoclusters. [Internet] [Masters thesis]. University of Texas – Austin; 2013. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2152/27207.

Council of Science Editors:

Dinin AK. The manufacture and characterization of protein nanoclusters. [Masters Thesis]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/27207


Kansas State University

9. Wang, Yin. Characterization and application of monoclonal antibodies against porcine epidemic diarrhea virus.

Degree: MS, Department of Diagnostic Medicine and Pathobiology, 2015, Kansas State University

 Porcine epidemic diarrhea virus (PEDV) causes acute diarrhea to pigs at all ages, resulting in high mortality rate of 80-100% in piglets less than one… (more)

Subjects/Keywords: Porcine epidemic diarrhea virus; monoclonal antibody characterization; monoclonal antibody production; Virology (0720)

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APA (6th Edition):

Wang, Y. (2015). Characterization and application of monoclonal antibodies against porcine epidemic diarrhea virus. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/20588

Chicago Manual of Style (16th Edition):

Wang, Yin. “Characterization and application of monoclonal antibodies against porcine epidemic diarrhea virus.” 2015. Masters Thesis, Kansas State University. Accessed October 19, 2019. http://hdl.handle.net/2097/20588.

MLA Handbook (7th Edition):

Wang, Yin. “Characterization and application of monoclonal antibodies against porcine epidemic diarrhea virus.” 2015. Web. 19 Oct 2019.

Vancouver:

Wang Y. Characterization and application of monoclonal antibodies against porcine epidemic diarrhea virus. [Internet] [Masters thesis]. Kansas State University; 2015. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2097/20588.

Council of Science Editors:

Wang Y. Characterization and application of monoclonal antibodies against porcine epidemic diarrhea virus. [Masters Thesis]. Kansas State University; 2015. Available from: http://hdl.handle.net/2097/20588


University of Alberta

10. Ganguly, Advaita. Ultrasensitive Point-of-Care Dengue Diagnostics and Vaccine Applications.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2013, University of Alberta

 Dengue virus infections can result in a range of clinical manifestations from asymptomatic infection to dengue fever and the severe disease dengue haemorrhagic fever/dengue shock… (more)

Subjects/Keywords: Dengue; Bispecific Antibody; Immunoswab; Monoclonal Antibody; Chicken IgY

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APA (6th Edition):

Ganguly, A. (2013). Ultrasensitive Point-of-Care Dengue Diagnostics and Vaccine Applications. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/44558f63z

Chicago Manual of Style (16th Edition):

Ganguly, Advaita. “Ultrasensitive Point-of-Care Dengue Diagnostics and Vaccine Applications.” 2013. Doctoral Dissertation, University of Alberta. Accessed October 19, 2019. https://era.library.ualberta.ca/files/44558f63z.

MLA Handbook (7th Edition):

Ganguly, Advaita. “Ultrasensitive Point-of-Care Dengue Diagnostics and Vaccine Applications.” 2013. Web. 19 Oct 2019.

Vancouver:

Ganguly A. Ultrasensitive Point-of-Care Dengue Diagnostics and Vaccine Applications. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Oct 19]. Available from: https://era.library.ualberta.ca/files/44558f63z.

Council of Science Editors:

Ganguly A. Ultrasensitive Point-of-Care Dengue Diagnostics and Vaccine Applications. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/44558f63z

11. Heitzmann-Daverton, Adèle. Utilisation d'un anticorps monoclonal anti-Tn en immunothérapie des cancers : Use of a monoclonal antibody anti-Tn in cancer immunotherapy.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2013, Université Paris Descartes – Paris V

 La transformation des cellules normales de l’organisme en un phénotype malin est souvent accompagnée de changements dans leur antigénicité. L’antigène Tn (GalNac-O-Ser/Thréo) est un antigène… (more)

Subjects/Keywords: Anticorps monoclonal; Immunothérapie; Internalisation; Immunoconjugué; Saporine; Auristatine F; Monoclonal antibody; Immunotherapy; Internalization; 616.994

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APA (6th Edition):

Heitzmann-Daverton, A. (2013). Utilisation d'un anticorps monoclonal anti-Tn en immunothérapie des cancers : Use of a monoclonal antibody anti-Tn in cancer immunotherapy. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05T014

Chicago Manual of Style (16th Edition):

Heitzmann-Daverton, Adèle. “Utilisation d'un anticorps monoclonal anti-Tn en immunothérapie des cancers : Use of a monoclonal antibody anti-Tn in cancer immunotherapy.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 19, 2019. http://www.theses.fr/2013PA05T014.

MLA Handbook (7th Edition):

Heitzmann-Daverton, Adèle. “Utilisation d'un anticorps monoclonal anti-Tn en immunothérapie des cancers : Use of a monoclonal antibody anti-Tn in cancer immunotherapy.” 2013. Web. 19 Oct 2019.

Vancouver:

Heitzmann-Daverton A. Utilisation d'un anticorps monoclonal anti-Tn en immunothérapie des cancers : Use of a monoclonal antibody anti-Tn in cancer immunotherapy. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2019 Oct 19]. Available from: http://www.theses.fr/2013PA05T014.

Council of Science Editors:

Heitzmann-Daverton A. Utilisation d'un anticorps monoclonal anti-Tn en immunothérapie des cancers : Use of a monoclonal antibody anti-Tn in cancer immunotherapy. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05T014

12. Stella, Carolina Nigro. Produção, caracterização e aplicação analítica de anticorpos monoclonais anti-β2-glicoproteína I.

Degree: Mestrado, Análises Clínicas, 2010, University of São Paulo

Anticorpos monoclonais (AcMo) anti-β2GPI foram obtidos de hibridomas produzidos pela fusão de linfócitos de camundongos com células SP2-O, de mieloma murino. A imunização foi realizada… (more)

Subjects/Keywords: β; 2-glicoproteína I; β; 2-glycoprotein I; Anticorpo monoclonal; ELISA; ELISA; Immunohistochemistry; Imuno-histoquímica; Monoclonal antibody

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APA (6th Edition):

Stella, C. N. (2010). Produção, caracterização e aplicação analítica de anticorpos monoclonais anti-β2-glicoproteína I. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22042010-103017/ ;

Chicago Manual of Style (16th Edition):

Stella, Carolina Nigro. “Produção, caracterização e aplicação analítica de anticorpos monoclonais anti-β2-glicoproteína I.” 2010. Masters Thesis, University of São Paulo. Accessed October 19, 2019. http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22042010-103017/ ;.

MLA Handbook (7th Edition):

Stella, Carolina Nigro. “Produção, caracterização e aplicação analítica de anticorpos monoclonais anti-β2-glicoproteína I.” 2010. Web. 19 Oct 2019.

Vancouver:

Stella CN. Produção, caracterização e aplicação analítica de anticorpos monoclonais anti-β2-glicoproteína I. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2019 Oct 19]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22042010-103017/ ;.

Council of Science Editors:

Stella CN. Produção, caracterização e aplicação analítica de anticorpos monoclonais anti-β2-glicoproteína I. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22042010-103017/ ;

13. Mororó, Janio da Silva. Estudo de marcação do anticorpo monoclonal anti-PBP2a com 99mTc.

Degree: Mestrado, Tecnologia Nuclear - Aplicações, 2012, University of São Paulo

Staphylococcus aureus é um dos principais microorganismos causadores de infecção em humanos, podendo causar inclusive bacteremia e endocardite nos indivíduos infectados. Diversas cepas desta bactéria… (more)

Subjects/Keywords: 99mTc; 99mTc; anticorpo monoclonal; diagnosis; diagnóstico; hospital infecious; infecção hospitalar; monoclonal antibody; MRSA; MRSA

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APA (6th Edition):

Mororó, J. d. S. (2012). Estudo de marcação do anticorpo monoclonal anti-PBP2a com 99mTc. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/85/85131/tde-06032013-151412/ ;

Chicago Manual of Style (16th Edition):

Mororó, Janio da Silva. “Estudo de marcação do anticorpo monoclonal anti-PBP2a com 99mTc.” 2012. Masters Thesis, University of São Paulo. Accessed October 19, 2019. http://www.teses.usp.br/teses/disponiveis/85/85131/tde-06032013-151412/ ;.

MLA Handbook (7th Edition):

Mororó, Janio da Silva. “Estudo de marcação do anticorpo monoclonal anti-PBP2a com 99mTc.” 2012. Web. 19 Oct 2019.

Vancouver:

Mororó JdS. Estudo de marcação do anticorpo monoclonal anti-PBP2a com 99mTc. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2019 Oct 19]. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-06032013-151412/ ;.

Council of Science Editors:

Mororó JdS. Estudo de marcação do anticorpo monoclonal anti-PBP2a com 99mTc. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-06032013-151412/ ;

14. Anjos, Fabyana Maria dos. Desenvolvimento de técnicas de imunoensaio para detecção de microcistina em amostras ambientais.

Degree: PhD, Análises Clínicas, 2009, University of São Paulo

A contaminação da água para consumo humano por toxinas produzidas por cianobactérias é um problema de saúde pública e das autoridades em todo o mundo.… (more)

Subjects/Keywords: Anticorpo monoclonal; Anticorpo policlonal; Conjugação de peptídeos; ELISA; ELISA; Hibridoma; Hybridoma; Microcistina; Microcystin; Monoclonal antibody; Nodularin; Nodularina; Peptide conjugation; Polyclonal antibody

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APA (6th Edition):

Anjos, F. M. d. (2009). Desenvolvimento de técnicas de imunoensaio para detecção de microcistina em amostras ambientais. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22122009-103848/ ;

Chicago Manual of Style (16th Edition):

Anjos, Fabyana Maria dos. “Desenvolvimento de técnicas de imunoensaio para detecção de microcistina em amostras ambientais.” 2009. Doctoral Dissertation, University of São Paulo. Accessed October 19, 2019. http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22122009-103848/ ;.

MLA Handbook (7th Edition):

Anjos, Fabyana Maria dos. “Desenvolvimento de técnicas de imunoensaio para detecção de microcistina em amostras ambientais.” 2009. Web. 19 Oct 2019.

Vancouver:

Anjos FMd. Desenvolvimento de técnicas de imunoensaio para detecção de microcistina em amostras ambientais. [Internet] [Doctoral dissertation]. University of São Paulo; 2009. [cited 2019 Oct 19]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22122009-103848/ ;.

Council of Science Editors:

Anjos FMd. Desenvolvimento de técnicas de imunoensaio para detecção de microcistina em amostras ambientais. [Doctoral Dissertation]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/9/9136/tde-22122009-103848/ ;


University of Oxford

15. Baruah, Kavitha. Structural biology of IgG Fc glycoforms.

Degree: PhD, 2012, University of Oxford

 The conserved N-linked glycosylation site on the Fc domain of IgG1 antibodies is essential for maintaining a functionally active conformation of the antibody. Different glycoforms… (more)

Subjects/Keywords: 572.6; Biochemistry; Glycobiology; Immunology; monoclonal antibodies; antibody glycosylation; endoglycosidase S; antibody glycoforms

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

APA (6th Edition):

Baruah, K. (2012). Structural biology of IgG Fc glycoforms. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:def683d3-aa06-41d9-9f28-29d21258bebe ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559735

Chicago Manual of Style (16th Edition):

Baruah, Kavitha. “Structural biology of IgG Fc glycoforms.” 2012. Doctoral Dissertation, University of Oxford. Accessed October 19, 2019. http://ora.ox.ac.uk/objects/uuid:def683d3-aa06-41d9-9f28-29d21258bebe ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559735.

MLA Handbook (7th Edition):

Baruah, Kavitha. “Structural biology of IgG Fc glycoforms.” 2012. Web. 19 Oct 2019.

Vancouver:

Baruah K. Structural biology of IgG Fc glycoforms. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Oct 19]. Available from: http://ora.ox.ac.uk/objects/uuid:def683d3-aa06-41d9-9f28-29d21258bebe ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559735.

Council of Science Editors:

Baruah K. Structural biology of IgG Fc glycoforms. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:def683d3-aa06-41d9-9f28-29d21258bebe ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559735


University of Edinburgh

16. Bell, Graham Thomas. Studies on the production of human monoclonal antibodies.

Degree: PhD, 1988, University of Edinburgh

Subjects/Keywords: 610; Monoclonal antibody production

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

APA (6th Edition):

Bell, G. T. (1988). Studies on the production of human monoclonal antibodies. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/19241

Chicago Manual of Style (16th Edition):

Bell, Graham Thomas. “Studies on the production of human monoclonal antibodies.” 1988. Doctoral Dissertation, University of Edinburgh. Accessed October 19, 2019. http://hdl.handle.net/1842/19241.

MLA Handbook (7th Edition):

Bell, Graham Thomas. “Studies on the production of human monoclonal antibodies.” 1988. Web. 19 Oct 2019.

Vancouver:

Bell GT. Studies on the production of human monoclonal antibodies. [Internet] [Doctoral dissertation]. University of Edinburgh; 1988. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/1842/19241.

Council of Science Editors:

Bell GT. Studies on the production of human monoclonal antibodies. [Doctoral Dissertation]. University of Edinburgh; 1988. Available from: http://hdl.handle.net/1842/19241


University of Kentucky

17. Weng, Chu-Chun. DEVELOPMENT AND CHARACTERIZATION OF NOVEL MONOCLONAL ANTIBODIES FOR STUDYING PRION PATHOGENESIS.

Degree: 2011, University of Kentucky

Monoclonal antibodies (mAbs) recognizing different regions of PrP are potential tools in the study of prion diseases and immunotherapy. We used shuffled recombinant prion protein… (more)

Subjects/Keywords: Prion; epitope; Monoclonal antibody; Medicine and Health Sciences

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

APA (6th Edition):

Weng, C. (2011). DEVELOPMENT AND CHARACTERIZATION OF NOVEL MONOCLONAL ANTIBODIES FOR STUDYING PRION PATHOGENESIS. (Masters Thesis). University of Kentucky. Retrieved from http://uknowledge.uky.edu/gradschool_theses/95

Chicago Manual of Style (16th Edition):

Weng, Chu-Chun. “DEVELOPMENT AND CHARACTERIZATION OF NOVEL MONOCLONAL ANTIBODIES FOR STUDYING PRION PATHOGENESIS.” 2011. Masters Thesis, University of Kentucky. Accessed October 19, 2019. http://uknowledge.uky.edu/gradschool_theses/95.

MLA Handbook (7th Edition):

Weng, Chu-Chun. “DEVELOPMENT AND CHARACTERIZATION OF NOVEL MONOCLONAL ANTIBODIES FOR STUDYING PRION PATHOGENESIS.” 2011. Web. 19 Oct 2019.

Vancouver:

Weng C. DEVELOPMENT AND CHARACTERIZATION OF NOVEL MONOCLONAL ANTIBODIES FOR STUDYING PRION PATHOGENESIS. [Internet] [Masters thesis]. University of Kentucky; 2011. [cited 2019 Oct 19]. Available from: http://uknowledge.uky.edu/gradschool_theses/95.

Council of Science Editors:

Weng C. DEVELOPMENT AND CHARACTERIZATION OF NOVEL MONOCLONAL ANTIBODIES FOR STUDYING PRION PATHOGENESIS. [Masters Thesis]. University of Kentucky; 2011. Available from: http://uknowledge.uky.edu/gradschool_theses/95

18. Schmidt, Stefan. Merger and acquisition between small biotech and large pharmaceutical companies - a winning combination? : Case study on the acquisitions of CAT by AstraZeneca and Abgenix by Amgen; MBA thesis in marketing.

Degree: Business Administration and Economics, 2008, University of Gävle

  This study aims at introducing and describing a novel multi parameter analysis method to identify potential acquisition targets and to qualitatively and quantitatively evaluate… (more)

Subjects/Keywords: Merger and acquisition; biotechnology; pharmaceutical industry; monoclonal antibody; Business studies; Företagsekonomi

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APA (6th Edition):

Schmidt, S. (2008). Merger and acquisition between small biotech and large pharmaceutical companies - a winning combination? : Case study on the acquisitions of CAT by AstraZeneca and Abgenix by Amgen; MBA thesis in marketing. (Thesis). University of Gävle. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-3261

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):

Schmidt, Stefan. “Merger and acquisition between small biotech and large pharmaceutical companies - a winning combination? : Case study on the acquisitions of CAT by AstraZeneca and Abgenix by Amgen; MBA thesis in marketing.” 2008. Thesis, University of Gävle. Accessed October 19, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-3261.

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

MLA Handbook (7th Edition):

Schmidt, Stefan. “Merger and acquisition between small biotech and large pharmaceutical companies - a winning combination? : Case study on the acquisitions of CAT by AstraZeneca and Abgenix by Amgen; MBA thesis in marketing.” 2008. Web. 19 Oct 2019.

Vancouver:

Schmidt S. Merger and acquisition between small biotech and large pharmaceutical companies - a winning combination? : Case study on the acquisitions of CAT by AstraZeneca and Abgenix by Amgen; MBA thesis in marketing. [Internet] [Thesis]. University of Gävle; 2008. [cited 2019 Oct 19]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-3261.

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

Council of Science Editors:

Schmidt S. Merger and acquisition between small biotech and large pharmaceutical companies - a winning combination? : Case study on the acquisitions of CAT by AstraZeneca and Abgenix by Amgen; MBA thesis in marketing. [Thesis]. University of Gävle; 2008. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hig:diva-3261

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

19. Beckford Vera Denis Rolando. Synthesis and evaluation of radioconjugates formed with selected trivalent radiometals .

Degree: 2011, Czech University of Technology

Synthesis and evaluation of radioconjugates; Synthesis and evaluation of radioconjutates Advisors/Committee Members: Melichar František (advisor).

Subjects/Keywords: Conjugation; Radiolabeling; Monoclonal antibody; Radiometals

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APA (6th Edition):

Rolando, B. V. D. (2011). Synthesis and evaluation of radioconjugates formed with selected trivalent radiometals . (Thesis). Czech University of Technology. Retrieved from http://hdl.handle.net/10467/8048

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):

Rolando, Beckford Vera Denis. “Synthesis and evaluation of radioconjugates formed with selected trivalent radiometals .” 2011. Thesis, Czech University of Technology. Accessed October 19, 2019. http://hdl.handle.net/10467/8048.

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

MLA Handbook (7th Edition):

Rolando, Beckford Vera Denis. “Synthesis and evaluation of radioconjugates formed with selected trivalent radiometals .” 2011. Web. 19 Oct 2019.

Vancouver:

Rolando BVD. Synthesis and evaluation of radioconjugates formed with selected trivalent radiometals . [Internet] [Thesis]. Czech University of Technology; 2011. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/10467/8048.

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

Council of Science Editors:

Rolando BVD. Synthesis and evaluation of radioconjugates formed with selected trivalent radiometals . [Thesis]. Czech University of Technology; 2011. Available from: http://hdl.handle.net/10467/8048

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


University of Alberta

20. Arefanian, Hossein. Tolerance to neonatal porcine islet xenografts induced by a combination of monoclonal antibodies.

Degree: PhD, Department of Surgery, 2009, University of Alberta

 Islet transplantation is a more physiological way to treat type 1 diabetes. However, shortage of donor tissue and chronic administration of immune suppressive drugs has… (more)

Subjects/Keywords: Monoclonal antibody; Neonatal porcine islets; Xenotransplantation; Islet transplantation; Tolerance

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

APA (6th Edition):

Arefanian, H. (2009). Tolerance to neonatal porcine islet xenografts induced by a combination of monoclonal antibodies. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/dv13zv40m

Chicago Manual of Style (16th Edition):

Arefanian, Hossein. “Tolerance to neonatal porcine islet xenografts induced by a combination of monoclonal antibodies.” 2009. Doctoral Dissertation, University of Alberta. Accessed October 19, 2019. https://era.library.ualberta.ca/files/dv13zv40m.

MLA Handbook (7th Edition):

Arefanian, Hossein. “Tolerance to neonatal porcine islet xenografts induced by a combination of monoclonal antibodies.” 2009. Web. 19 Oct 2019.

Vancouver:

Arefanian H. Tolerance to neonatal porcine islet xenografts induced by a combination of monoclonal antibodies. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2019 Oct 19]. Available from: https://era.library.ualberta.ca/files/dv13zv40m.

Council of Science Editors:

Arefanian H. Tolerance to neonatal porcine islet xenografts induced by a combination of monoclonal antibodies. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/dv13zv40m


University of Alberta

21. Newa,Madhuri. Antibody mediated “Universal” Osteoclast targeting platform.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2013, University of Alberta

 Osteoclasts are the sole cells responsible for bone resorption and their activity is central to the process of bone remodeling. Excessive osteoclast activity leads to… (more)

Subjects/Keywords: Monoclonal antibody; Osteoclast; RANK receptor; Single chain Fraction variable

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

APA (6th Edition):

Newa,Madhuri. (2013). Antibody mediated “Universal” Osteoclast targeting platform. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/jm214p61p

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

Chicago Manual of Style (16th Edition):

Newa,Madhuri. “Antibody mediated “Universal” Osteoclast targeting platform.” 2013. Doctoral Dissertation, University of Alberta. Accessed October 19, 2019. https://era.library.ualberta.ca/files/jm214p61p.

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

MLA Handbook (7th Edition):

Newa,Madhuri. “Antibody mediated “Universal” Osteoclast targeting platform.” 2013. Web. 19 Oct 2019.

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

Vancouver:

Newa,Madhuri. Antibody mediated “Universal” Osteoclast targeting platform. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Oct 19]. Available from: https://era.library.ualberta.ca/files/jm214p61p.

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

Council of Science Editors:

Newa,Madhuri. Antibody mediated “Universal” Osteoclast targeting platform. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/jm214p61p

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

22. Akita, Shin. MT95-4, a fully humanized antibody raised against aminopeptidase N, reduces tumor progression in a mouse model. : 完全ヒト型抗アミノペプチダーゼN抗体であるMT95-4は、マウスモデルにおいて腫瘍の進展を抑制する.

Degree: 博士(医学), 2015, Hiroshima University / 広島大学

 Cancer Sci 106 (2015) .p921–928Cancer Science published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Cancer Association. This is an open access article… (more)

Subjects/Keywords: Aminopeptidase N; angiogenesis; fully humanized monoclonal antibody; invasion; tumor growth

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APA (6th Edition):

Akita, S. (2015). MT95-4, a fully humanized antibody raised against aminopeptidase N, reduces tumor progression in a mouse model. : 完全ヒト型抗アミノペプチダーゼN抗体であるMT95-4は、マウスモデルにおいて腫瘍の進展を抑制する. (Thesis). Hiroshima University / 広島大学. Retrieved from http://ir.lib.hiroshima-u.ac.jp/00044053

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):

Akita, Shin. “MT95-4, a fully humanized antibody raised against aminopeptidase N, reduces tumor progression in a mouse model. : 完全ヒト型抗アミノペプチダーゼN抗体であるMT95-4は、マウスモデルにおいて腫瘍の進展を抑制する.” 2015. Thesis, Hiroshima University / 広島大学. Accessed October 19, 2019. http://ir.lib.hiroshima-u.ac.jp/00044053.

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

MLA Handbook (7th Edition):

Akita, Shin. “MT95-4, a fully humanized antibody raised against aminopeptidase N, reduces tumor progression in a mouse model. : 完全ヒト型抗アミノペプチダーゼN抗体であるMT95-4は、マウスモデルにおいて腫瘍の進展を抑制する.” 2015. Web. 19 Oct 2019.

Vancouver:

Akita S. MT95-4, a fully humanized antibody raised against aminopeptidase N, reduces tumor progression in a mouse model. : 完全ヒト型抗アミノペプチダーゼN抗体であるMT95-4は、マウスモデルにおいて腫瘍の進展を抑制する. [Internet] [Thesis]. Hiroshima University / 広島大学; 2015. [cited 2019 Oct 19]. Available from: http://ir.lib.hiroshima-u.ac.jp/00044053.

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

Council of Science Editors:

Akita S. MT95-4, a fully humanized antibody raised against aminopeptidase N, reduces tumor progression in a mouse model. : 完全ヒト型抗アミノペプチダーゼN抗体であるMT95-4は、マウスモデルにおいて腫瘍の進展を抑制する. [Thesis]. Hiroshima University / 広島大学; 2015. Available from: http://ir.lib.hiroshima-u.ac.jp/00044053

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

23. Prem Kumar, B. Production of monoclonal antibody using a cryogel based mini bioreactor system; -.

Degree: Bioseparation Technology, 2013, VIT University

Abstract avlible

Reference and Publication given

Advisors/Committee Members: Jayaprakash, N S.

Subjects/Keywords: antibody; bioreactor system; monoclonal; Production

Page 1

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APA (6th Edition):

Prem Kumar, B. (2013). Production of monoclonal antibody using a cryogel based mini bioreactor system; -. (Thesis). VIT University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/37753

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):

Prem Kumar, B. “Production of monoclonal antibody using a cryogel based mini bioreactor system; -.” 2013. Thesis, VIT University. Accessed October 19, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/37753.

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

MLA Handbook (7th Edition):

Prem Kumar, B. “Production of monoclonal antibody using a cryogel based mini bioreactor system; -.” 2013. Web. 19 Oct 2019.

Vancouver:

Prem Kumar B. Production of monoclonal antibody using a cryogel based mini bioreactor system; -. [Internet] [Thesis]. VIT University; 2013. [cited 2019 Oct 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37753.

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

Council of Science Editors:

Prem Kumar B. Production of monoclonal antibody using a cryogel based mini bioreactor system; -. [Thesis]. VIT University; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/37753

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


The Ohio State University

24. Mehta, Payal. Molecular Analysis of Regulation of Macrophage Fc¿ Receptor Function: Implications for Tumor Immunotherapy.

Degree: PhD, Biochemistry Program, Ohio State, 2011, The Ohio State University

 Therapeutic monoclonal antibodies (MAB) are used as a part of induction as well as salvage regimen for treatments of various malignancies. Despite a large number… (more)

Subjects/Keywords: Immunology; Fc&947; R, tumor immunotherapy, monoclonal antibody, SHIP

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APA (6th Edition):

Mehta, P. (2011). Molecular Analysis of Regulation of Macrophage Fc¿ Receptor Function: Implications for Tumor Immunotherapy. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1313606589

Chicago Manual of Style (16th Edition):

Mehta, Payal. “Molecular Analysis of Regulation of Macrophage Fc¿ Receptor Function: Implications for Tumor Immunotherapy.” 2011. Doctoral Dissertation, The Ohio State University. Accessed October 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1313606589.

MLA Handbook (7th Edition):

Mehta, Payal. “Molecular Analysis of Regulation of Macrophage Fc¿ Receptor Function: Implications for Tumor Immunotherapy.” 2011. Web. 19 Oct 2019.

Vancouver:

Mehta P. Molecular Analysis of Regulation of Macrophage Fc¿ Receptor Function: Implications for Tumor Immunotherapy. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Oct 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313606589.

Council of Science Editors:

Mehta P. Molecular Analysis of Regulation of Macrophage Fc¿ Receptor Function: Implications for Tumor Immunotherapy. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1313606589


NSYSU

25. Huang, Bo-cheng. To investigate the mechanism of protease-enhanced antibody activity to increase its therapeutic efficacy.

Degree: Master, Institute of Biomedical Sciences, 2014, NSYSU

Monoclonal antibody has become clinical medicine of a variety of disease widely. According to the statistics of drug use, monoclonal antibody therapies apply to cancer,… (more)

Subjects/Keywords: Monoclonal antibody; specificity; Cancer; Autoimmune disease; Targeted therapy

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APA (6th Edition):

Huang, B. (2014). To investigate the mechanism of protease-enhanced antibody activity to increase its therapeutic efficacy. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725114-101402

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):

Huang, Bo-cheng. “To investigate the mechanism of protease-enhanced antibody activity to increase its therapeutic efficacy.” 2014. Thesis, NSYSU. Accessed October 19, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725114-101402.

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

MLA Handbook (7th Edition):

Huang, Bo-cheng. “To investigate the mechanism of protease-enhanced antibody activity to increase its therapeutic efficacy.” 2014. Web. 19 Oct 2019.

Vancouver:

Huang B. To investigate the mechanism of protease-enhanced antibody activity to increase its therapeutic efficacy. [Internet] [Thesis]. NSYSU; 2014. [cited 2019 Oct 19]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725114-101402.

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

Council of Science Editors:

Huang B. To investigate the mechanism of protease-enhanced antibody activity to increase its therapeutic efficacy. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725114-101402

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


Universiteit Utrecht

26. Karambela, A.E. The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers.

Degree: 2010, Universiteit Utrecht

 The vertebrate immune system has evolved to become particularly good at protecting an organism from extrinsic pathogens such as bacterial and fungal infections. Today the… (more)

Subjects/Keywords: pharmacogenetics; fc receptor; monoclonal antibody; mAB; cancer; polymorphism

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APA (6th Edition):

Karambela, A. E. (2010). The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/188148

Chicago Manual of Style (16th Edition):

Karambela, A E. “The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers.” 2010. Masters Thesis, Universiteit Utrecht. Accessed October 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/188148.

MLA Handbook (7th Edition):

Karambela, A E. “The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers.” 2010. Web. 19 Oct 2019.

Vancouver:

Karambela AE. The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers. [Internet] [Masters thesis]. Universiteit Utrecht; 2010. [cited 2019 Oct 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/188148.

Council of Science Editors:

Karambela AE. The Pharmacogenetics behind Polymorphisms of the Immunoglobin G Fragment C Receptor and Efficacy of Monoclonal Antibody Treatments for Different Cancers. [Masters Thesis]. Universiteit Utrecht; 2010. Available from: http://dspace.library.uu.nl:8080/handle/1874/188148

27. 유, 화니. Production and Characterization of an Human Monoclonal Antibody IgG to TRAIL Receptor 2.

Degree: 2012, Ajou University

Tumor Necrosis Factor (TNF)-Related Apoptosis-Inducing Ligand (TRAIL) 은 TNF superfamily에 속하며, 수용성 TRAIL의 경우 DR4와 DR5및 결합하여 다양한 암세포에 세포독성을 가질 뿐 만 아니라, 정상세포에서는… (more)

Subjects/Keywords: TRAIL receptor 2; human agonistic monoclonal antibody IgG

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

APA (6th Edition):

유, . (2012). Production and Characterization of an Human Monoclonal Antibody IgG to TRAIL Receptor 2. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/7536 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012359

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):

유, 화니. “Production and Characterization of an Human Monoclonal Antibody IgG to TRAIL Receptor 2.” 2012. Thesis, Ajou University. Accessed October 19, 2019. http://repository.ajou.ac.kr/handle/201003/7536 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012359.

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

MLA Handbook (7th Edition):

유, 화니. “Production and Characterization of an Human Monoclonal Antibody IgG to TRAIL Receptor 2.” 2012. Web. 19 Oct 2019.

Vancouver:

유 . Production and Characterization of an Human Monoclonal Antibody IgG to TRAIL Receptor 2. [Internet] [Thesis]. Ajou University; 2012. [cited 2019 Oct 19]. Available from: http://repository.ajou.ac.kr/handle/201003/7536 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012359.

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

Council of Science Editors:

유 . Production and Characterization of an Human Monoclonal Antibody IgG to TRAIL Receptor 2. [Thesis]. Ajou University; 2012. Available from: http://repository.ajou.ac.kr/handle/201003/7536 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000012359

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


University of Gothenburg / Göteborgs Universitet

28. Werthén, Maria, 1957-. Immunochemistry at solid-liquid interfaces : a study of the binding reaction of monoclonal anti-DNP IgG-antibodies.

Degree: 1993, University of Gothenburg / Göteborgs Universitet

Subjects/Keywords: Antibodies; monoclonal; Antibody; affinity

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

APA (6th Edition):

Werthén, Maria, 1. (1993). Immunochemistry at solid-liquid interfaces : a study of the binding reaction of monoclonal anti-DNP IgG-antibodies. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/14884

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):

Werthén, Maria, 1957-. “Immunochemistry at solid-liquid interfaces : a study of the binding reaction of monoclonal anti-DNP IgG-antibodies.” 1993. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 19, 2019. http://hdl.handle.net/2077/14884.

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

MLA Handbook (7th Edition):

Werthén, Maria, 1957-. “Immunochemistry at solid-liquid interfaces : a study of the binding reaction of monoclonal anti-DNP IgG-antibodies.” 1993. Web. 19 Oct 2019.

Vancouver:

Werthén, Maria 1. Immunochemistry at solid-liquid interfaces : a study of the binding reaction of monoclonal anti-DNP IgG-antibodies. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 1993. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/2077/14884.

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

Council of Science Editors:

Werthén, Maria 1. Immunochemistry at solid-liquid interfaces : a study of the binding reaction of monoclonal anti-DNP IgG-antibodies. [Thesis]. University of Gothenburg / Göteborgs Universitet; 1993. Available from: http://hdl.handle.net/2077/14884

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


The Ohio State University

29. Mao, Yicheng. Monoclonal Antibody and Liposomal Nanoparticle-based Targeting Therapies for Chronic Lymphocytic Leukemia.

Degree: PhD, Pharmacy, 2012, The Ohio State University

 Chronic Lymphocytic Leukemia (CLL), representing 30% of leukemia, remains the most common hematologic malignancy in the western world. It is diagnosed by peripheral blood immunophenotyping… (more)

Subjects/Keywords: Pharmaceuticals; Chronic Lymphocytic Leukemia; Monoclonal Antibody; Liposomal Nanoparticles; Targeted Therapeutics

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

APA (6th Edition):

Mao, Y. (2012). Monoclonal Antibody and Liposomal Nanoparticle-based Targeting Therapies for Chronic Lymphocytic Leukemia. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1354299911

Chicago Manual of Style (16th Edition):

Mao, Yicheng. “Monoclonal Antibody and Liposomal Nanoparticle-based Targeting Therapies for Chronic Lymphocytic Leukemia.” 2012. Doctoral Dissertation, The Ohio State University. Accessed October 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1354299911.

MLA Handbook (7th Edition):

Mao, Yicheng. “Monoclonal Antibody and Liposomal Nanoparticle-based Targeting Therapies for Chronic Lymphocytic Leukemia.” 2012. Web. 19 Oct 2019.

Vancouver:

Mao Y. Monoclonal Antibody and Liposomal Nanoparticle-based Targeting Therapies for Chronic Lymphocytic Leukemia. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2019 Oct 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1354299911.

Council of Science Editors:

Mao Y. Monoclonal Antibody and Liposomal Nanoparticle-based Targeting Therapies for Chronic Lymphocytic Leukemia. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1354299911


University of Edinburgh

30. Sinclair, Elizabeth Hannah. Characterization of the IFITM1 signaling pathway in cancer.

Degree: PhD, 2016, University of Edinburgh

 The aim of this thesis was to establish the therapeutic value of the IFITM1 monoclonal antibodies and to design and develop therapeutically valuable recombinant monoclonal(more)

Subjects/Keywords: IFITM1; monoclonal antibodies; IRF1 pathway; IFITM1 antibody; immunotherapeutics

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

APA (6th Edition):

Sinclair, E. H. (2016). Characterization of the IFITM1 signaling pathway in cancer. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25780

Chicago Manual of Style (16th Edition):

Sinclair, Elizabeth Hannah. “Characterization of the IFITM1 signaling pathway in cancer.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed October 19, 2019. http://hdl.handle.net/1842/25780.

MLA Handbook (7th Edition):

Sinclair, Elizabeth Hannah. “Characterization of the IFITM1 signaling pathway in cancer.” 2016. Web. 19 Oct 2019.

Vancouver:

Sinclair EH. Characterization of the IFITM1 signaling pathway in cancer. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Oct 19]. Available from: http://hdl.handle.net/1842/25780.

Council of Science Editors:

Sinclair EH. Characterization of the IFITM1 signaling pathway in cancer. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25780

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