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You searched for subject:(phage display). Showing records 1 – 30 of 239 total matches.

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University of Waterloo

1. El-Zarkout, Farah. Design, construction and characterization of LysK endolysin display phage against Staphylococcus aureus.

Degree: 2014, University of Waterloo

 The growing threat of drug- resistant Staphylococcus aureus (S. aureus) infections mandates the need to develop novel, effective and alternative antibacterial therapeutics. Despite infection prevention… (more)

Subjects/Keywords: Bacteriophage; Phage Display; Staphylococcus aureus

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

APA (6th Edition):

El-Zarkout, F. (2014). Design, construction and characterization of LysK endolysin display phage against Staphylococcus aureus. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/8246

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):

El-Zarkout, Farah. “Design, construction and characterization of LysK endolysin display phage against Staphylococcus aureus.” 2014. Thesis, University of Waterloo. Accessed January 22, 2020. http://hdl.handle.net/10012/8246.

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

MLA Handbook (7th Edition):

El-Zarkout, Farah. “Design, construction and characterization of LysK endolysin display phage against Staphylococcus aureus.” 2014. Web. 22 Jan 2020.

Vancouver:

El-Zarkout F. Design, construction and characterization of LysK endolysin display phage against Staphylococcus aureus. [Internet] [Thesis]. University of Waterloo; 2014. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10012/8246.

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

Council of Science Editors:

El-Zarkout F. Design, construction and characterization of LysK endolysin display phage against Staphylococcus aureus. [Thesis]. University of Waterloo; 2014. Available from: http://hdl.handle.net/10012/8246

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

2. Gomes, Margarida. Développement de bibliothèques de protéines artificielles permettant la création d’outils de reconnaissance moléculaire innovants : Development of artificial protein libraries for the creation of innovative molecular recognition tools.

Degree: Docteur es, Biochimie et biologie structurale, 2018, Paris Saclay

Le travail de thèse présente une approche innovante pour la construction d’une bibliothèque de protéines basées sur l’ossature protéique. L’objectif est de générer une source… (more)

Subjects/Keywords: Bibliothèques; Protéines Artificielles; Phage Display; Libraries; Artifficial proteins; Phage display

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APA (6th Edition):

Gomes, M. (2018). Développement de bibliothèques de protéines artificielles permettant la création d’outils de reconnaissance moléculaire innovants : Development of artificial protein libraries for the creation of innovative molecular recognition tools. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS030

Chicago Manual of Style (16th Edition):

Gomes, Margarida. “Développement de bibliothèques de protéines artificielles permettant la création d’outils de reconnaissance moléculaire innovants : Development of artificial protein libraries for the creation of innovative molecular recognition tools.” 2018. Doctoral Dissertation, Paris Saclay. Accessed January 22, 2020. http://www.theses.fr/2018SACLS030.

MLA Handbook (7th Edition):

Gomes, Margarida. “Développement de bibliothèques de protéines artificielles permettant la création d’outils de reconnaissance moléculaire innovants : Development of artificial protein libraries for the creation of innovative molecular recognition tools.” 2018. Web. 22 Jan 2020.

Vancouver:

Gomes M. Développement de bibliothèques de protéines artificielles permettant la création d’outils de reconnaissance moléculaire innovants : Development of artificial protein libraries for the creation of innovative molecular recognition tools. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2018SACLS030.

Council of Science Editors:

Gomes M. Développement de bibliothèques de protéines artificielles permettant la création d’outils de reconnaissance moléculaire innovants : Development of artificial protein libraries for the creation of innovative molecular recognition tools. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS030


Université Paris-Sud – Paris XI

3. Nangola, Sawitree. The interference of human immunodeficiency virus assembly and maturation by ankyrin repeat proteins : Interférences avec l'assemblage et la maturation du Virus de l'Immunodeficience Humaine (VIH) par des protéines à motifs répétés Ankyrines.

Degree: Docteur es, Biologie, 2011, Université Paris-Sud – Paris XI

Le but de ce travail est de découvrir des nouvelles protéines suceptibles d'interférer avec le cycle vital du virus HIV. De par leur repliement, les… (more)

Subjects/Keywords: Ankynine; Phage display; Vih; Ankyrines; Phage display; Vih

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APA (6th Edition):

Nangola, S. (2011). The interference of human immunodeficiency virus assembly and maturation by ankyrin repeat proteins : Interférences avec l'assemblage et la maturation du Virus de l'Immunodeficience Humaine (VIH) par des protéines à motifs répétés Ankyrines. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112044

Chicago Manual of Style (16th Edition):

Nangola, Sawitree. “The interference of human immunodeficiency virus assembly and maturation by ankyrin repeat proteins : Interférences avec l'assemblage et la maturation du Virus de l'Immunodeficience Humaine (VIH) par des protéines à motifs répétés Ankyrines.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 22, 2020. http://www.theses.fr/2011PA112044.

MLA Handbook (7th Edition):

Nangola, Sawitree. “The interference of human immunodeficiency virus assembly and maturation by ankyrin repeat proteins : Interférences avec l'assemblage et la maturation du Virus de l'Immunodeficience Humaine (VIH) par des protéines à motifs répétés Ankyrines.” 2011. Web. 22 Jan 2020.

Vancouver:

Nangola S. The interference of human immunodeficiency virus assembly and maturation by ankyrin repeat proteins : Interférences avec l'assemblage et la maturation du Virus de l'Immunodeficience Humaine (VIH) par des protéines à motifs répétés Ankyrines. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2011PA112044.

Council of Science Editors:

Nangola S. The interference of human immunodeficiency virus assembly and maturation by ankyrin repeat proteins : Interférences avec l'assemblage et la maturation du Virus de l'Immunodeficience Humaine (VIH) par des protéines à motifs répétés Ankyrines. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112044


University of Edinburgh

4. Möller, Angeli. Development of an intrabody capable of activating interferon regulatory factor-1 (IRF-1) and identification of IRF-1-binding peptide motifs.

Degree: PhD, 2011, University of Edinburgh

 Interferon regulatory factor 1 (IRF-1) is a tumour suppressor protein and transcription factor. It has been shown to modulate target gene expression in response to… (more)

Subjects/Keywords: 616.994; IRF-1; intrabody; cancer; phage-display

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APA (6th Edition):

Möller, A. (2011). Development of an intrabody capable of activating interferon regulatory factor-1 (IRF-1) and identification of IRF-1-binding peptide motifs. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5590

Chicago Manual of Style (16th Edition):

Möller, Angeli. “Development of an intrabody capable of activating interferon regulatory factor-1 (IRF-1) and identification of IRF-1-binding peptide motifs.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed January 22, 2020. http://hdl.handle.net/1842/5590.

MLA Handbook (7th Edition):

Möller, Angeli. “Development of an intrabody capable of activating interferon regulatory factor-1 (IRF-1) and identification of IRF-1-binding peptide motifs.” 2011. Web. 22 Jan 2020.

Vancouver:

Möller A. Development of an intrabody capable of activating interferon regulatory factor-1 (IRF-1) and identification of IRF-1-binding peptide motifs. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/1842/5590.

Council of Science Editors:

Möller A. Development of an intrabody capable of activating interferon regulatory factor-1 (IRF-1) and identification of IRF-1-binding peptide motifs. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5590

5. Rafael Nascimento. Construção de uma biblioteca de anticorpos monoclonais apresentados em fagos para seleção e caracterização de scFv ligante a proteínas intestinais de Diatraea saccharalis.

Degree: 2009, Federal University of Uberlândia

A broca-da-cana, Diatraea saccharalis (Fabricius, 1794) (Lepidoptera: Crambidae), destaca-se como a praga que mais causa danos ao cultivo da cana-de-açúcar no Brasil e outras localidades… (more)

Subjects/Keywords: ScFv; Diatraea saccharalis; GENETICA; Phage display

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APA (6th Edition):

Nascimento, R. (2009). Construção de uma biblioteca de anticorpos monoclonais apresentados em fagos para seleção e caracterização de scFv ligante a proteínas intestinais de Diatraea saccharalis. (Thesis). Federal University of Uberlândia. Retrieved from http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=2880

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):

Nascimento, Rafael. “Construção de uma biblioteca de anticorpos monoclonais apresentados em fagos para seleção e caracterização de scFv ligante a proteínas intestinais de Diatraea saccharalis.” 2009. Thesis, Federal University of Uberlândia. Accessed January 22, 2020. http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=2880.

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

MLA Handbook (7th Edition):

Nascimento, Rafael. “Construção de uma biblioteca de anticorpos monoclonais apresentados em fagos para seleção e caracterização de scFv ligante a proteínas intestinais de Diatraea saccharalis.” 2009. Web. 22 Jan 2020.

Vancouver:

Nascimento R. Construção de uma biblioteca de anticorpos monoclonais apresentados em fagos para seleção e caracterização de scFv ligante a proteínas intestinais de Diatraea saccharalis. [Internet] [Thesis]. Federal University of Uberlândia; 2009. [cited 2020 Jan 22]. Available from: http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=2880.

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

Council of Science Editors:

Nascimento R. Construção de uma biblioteca de anticorpos monoclonais apresentados em fagos para seleção e caracterização de scFv ligante a proteínas intestinais de Diatraea saccharalis. [Thesis]. Federal University of Uberlândia; 2009. Available from: http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=2880

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

6. Paula de Souza Santos. Seleção e caracterização de peptídeos recombinantes miméticos de antígenos do vírus da dengue por "PHAGE DISPLAY".

Degree: 2006, Federal University of Uberlândia

 RESUMO - GERAL A dengue é uma doença infecciosa febril aguda, transmitida de uma pessoa doente a uma pessoa sadia pela picada da fêmea contaminada… (more)

Subjects/Keywords: GENETICA; Dengue; Phage Display; Anticorpo monoclonal

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APA (6th Edition):

Santos, P. d. S. (2006). Seleção e caracterização de peptídeos recombinantes miméticos de antígenos do vírus da dengue por "PHAGE DISPLAY". (Thesis). Federal University of Uberlândia. Retrieved from http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=472

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):

Santos, Paula de Souza. “Seleção e caracterização de peptídeos recombinantes miméticos de antígenos do vírus da dengue por "PHAGE DISPLAY".” 2006. Thesis, Federal University of Uberlândia. Accessed January 22, 2020. http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=472.

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

MLA Handbook (7th Edition):

Santos, Paula de Souza. “Seleção e caracterização de peptídeos recombinantes miméticos de antígenos do vírus da dengue por "PHAGE DISPLAY".” 2006. Web. 22 Jan 2020.

Vancouver:

Santos PdS. Seleção e caracterização de peptídeos recombinantes miméticos de antígenos do vírus da dengue por "PHAGE DISPLAY". [Internet] [Thesis]. Federal University of Uberlândia; 2006. [cited 2020 Jan 22]. Available from: http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=472.

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

Council of Science Editors:

Santos PdS. Seleção e caracterização de peptídeos recombinantes miméticos de antígenos do vírus da dengue por "PHAGE DISPLAY". [Thesis]. Federal University of Uberlândia; 2006. Available from: http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=472

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


University of New Mexico

7. Rogers, Jason Hugh. Development of CD19 binding reagents for targeted nanoparticles.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 B-cell malignancies like Acute Lymphoblastic Leukemia (B-ALL), which often have high numbers of malignant cells in circulation in the blood would be an excellent model… (more)

Subjects/Keywords: leukemia; CD19; nanoparticle; phage display; ScFv antibody

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APA (6th Edition):

Rogers, J. H. (2013). Development of CD19 binding reagents for targeted nanoparticles. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/73

Chicago Manual of Style (16th Edition):

Rogers, Jason Hugh. “Development of CD19 binding reagents for targeted nanoparticles.” 2013. Masters Thesis, University of New Mexico. Accessed January 22, 2020. https://digitalrepository.unm.edu/biom_etds/73.

MLA Handbook (7th Edition):

Rogers, Jason Hugh. “Development of CD19 binding reagents for targeted nanoparticles.” 2013. Web. 22 Jan 2020.

Vancouver:

Rogers JH. Development of CD19 binding reagents for targeted nanoparticles. [Internet] [Masters thesis]. University of New Mexico; 2013. [cited 2020 Jan 22]. Available from: https://digitalrepository.unm.edu/biom_etds/73.

Council of Science Editors:

Rogers JH. Development of CD19 binding reagents for targeted nanoparticles. [Masters Thesis]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/73


University of Oklahoma

8. Sunderland, Kegan. VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS.

Degree: PhD, 2018, University of Oklahoma

 Bone morphogenetic proteins (BMPs) are part of the transforming growth factor-β superfamily and function as key regulators of cellular growth, differentiation, and tissue formation. While… (more)

Subjects/Keywords: Tissue Regeneration; Phage Display; Growth factor mimetic

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APA (6th Edition):

Sunderland, K. (2018). VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/316302

Chicago Manual of Style (16th Edition):

Sunderland, Kegan. “VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS.” 2018. Doctoral Dissertation, University of Oklahoma. Accessed January 22, 2020. http://hdl.handle.net/11244/316302.

MLA Handbook (7th Edition):

Sunderland, Kegan. “VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS.” 2018. Web. 22 Jan 2020.

Vancouver:

Sunderland K. VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS. [Internet] [Doctoral dissertation]. University of Oklahoma; 2018. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/11244/316302.

Council of Science Editors:

Sunderland K. VIRUS-SELECTED OSTEOGENESIS-INDUCING PEPTIDES FOR ENHANCED BONE REGENERATION IN 3D PRINTED TITANIUM ALLOY IMPLANTS. [Doctoral Dissertation]. University of Oklahoma; 2018. Available from: http://hdl.handle.net/11244/316302


University of California – San Diego

9. Bahn, Adrian Jaemin. Examining the Phage and Ribosome Display of Diversity-Generating Retroelement Variable Proteins.

Degree: Biology, 2018, University of California – San Diego

 Diversity-generating retroelements (DGRs) are genetic modules with the ability to introduce massive sequence variation into specific target proteins. Such DGR variable proteins are able to… (more)

Subjects/Keywords: Biochemistry; Display; Diversity; Generating; Phage; Retroelement; Ribosome

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APA (6th Edition):

Bahn, A. J. (2018). Examining the Phage and Ribosome Display of Diversity-Generating Retroelement Variable Proteins. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9tb0s64d

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):

Bahn, Adrian Jaemin. “Examining the Phage and Ribosome Display of Diversity-Generating Retroelement Variable Proteins.” 2018. Thesis, University of California – San Diego. Accessed January 22, 2020. http://www.escholarship.org/uc/item/9tb0s64d.

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

MLA Handbook (7th Edition):

Bahn, Adrian Jaemin. “Examining the Phage and Ribosome Display of Diversity-Generating Retroelement Variable Proteins.” 2018. Web. 22 Jan 2020.

Vancouver:

Bahn AJ. Examining the Phage and Ribosome Display of Diversity-Generating Retroelement Variable Proteins. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Jan 22]. Available from: http://www.escholarship.org/uc/item/9tb0s64d.

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

Council of Science Editors:

Bahn AJ. Examining the Phage and Ribosome Display of Diversity-Generating Retroelement Variable Proteins. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/9tb0s64d

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


University of Saskatchewan

10. Hogan, Daniel. Applications of Machine Learning for Predicting Selection Outcomes in Antibody Phage Display.

Degree: 2016, University of Saskatchewan

 Antibodies form an essential component of the adaptive immune system, but they also have important scientific and clinical applications. These applications exploit the proven ability… (more)

Subjects/Keywords: Bioinformatics; Machine Learning; Antibodies; Antibody Phage Display

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APA (6th Edition):

Hogan, D. (2016). Applications of Machine Learning for Predicting Selection Outcomes in Antibody Phage Display. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7471

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):

Hogan, Daniel. “Applications of Machine Learning for Predicting Selection Outcomes in Antibody Phage Display.” 2016. Thesis, University of Saskatchewan. Accessed January 22, 2020. http://hdl.handle.net/10388/7471.

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

MLA Handbook (7th Edition):

Hogan, Daniel. “Applications of Machine Learning for Predicting Selection Outcomes in Antibody Phage Display.” 2016. Web. 22 Jan 2020.

Vancouver:

Hogan D. Applications of Machine Learning for Predicting Selection Outcomes in Antibody Phage Display. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10388/7471.

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

Council of Science Editors:

Hogan D. Applications of Machine Learning for Predicting Selection Outcomes in Antibody Phage Display. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7471

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


University of Saskatchewan

11. Fu, Yongpeng 1990-. Selection and Characterization of Synthetic Antibodies Against Human Rad51.

Degree: 2017, University of Saskatchewan

 Chemotherapy is the predominant approach for treating cancer. However, disease relapse frequently occurs because chemotherapy often fails to eliminate all tumor cells due to intrinsic… (more)

Subjects/Keywords: Phage display; Cancer; Rad51; Fab; Intracellular antibody

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APA (6th Edition):

Fu, Y. 1. (2017). Selection and Characterization of Synthetic Antibodies Against Human Rad51. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7766

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):

Fu, Yongpeng 1990-. “Selection and Characterization of Synthetic Antibodies Against Human Rad51.” 2017. Thesis, University of Saskatchewan. Accessed January 22, 2020. http://hdl.handle.net/10388/7766.

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

MLA Handbook (7th Edition):

Fu, Yongpeng 1990-. “Selection and Characterization of Synthetic Antibodies Against Human Rad51.” 2017. Web. 22 Jan 2020.

Vancouver:

Fu Y1. Selection and Characterization of Synthetic Antibodies Against Human Rad51. [Internet] [Thesis]. University of Saskatchewan; 2017. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10388/7766.

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

Council of Science Editors:

Fu Y1. Selection and Characterization of Synthetic Antibodies Against Human Rad51. [Thesis]. University of Saskatchewan; 2017. Available from: http://hdl.handle.net/10388/7766

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


Universitat de Valencia

12. Gozalbo Rovira, Roberto Vicente. Hacia la caracterización del epítopo del autoantígeno en el Síndrome de Goodpasture .

Degree: 2014, Universitat de Valencia

 El síndrome de Goodpasture (GP) es un desorden autoinmune que cursa con glomerulonefritis rápidamente progresiva y hemorragia pulmonar. El ataque inmunológico se lleva a cabo… (more)

Subjects/Keywords: epítopo; Autoinmune; Antígeno-anticuerpo; Goodpasture; phage display

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APA (6th Edition):

Gozalbo Rovira, R. V. (2014). Hacia la caracterización del epítopo del autoantígeno en el Síndrome de Goodpasture . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/40335

Chicago Manual of Style (16th Edition):

Gozalbo Rovira, Roberto Vicente. “Hacia la caracterización del epítopo del autoantígeno en el Síndrome de Goodpasture .” 2014. Doctoral Dissertation, Universitat de Valencia. Accessed January 22, 2020. http://hdl.handle.net/10550/40335.

MLA Handbook (7th Edition):

Gozalbo Rovira, Roberto Vicente. “Hacia la caracterización del epítopo del autoantígeno en el Síndrome de Goodpasture .” 2014. Web. 22 Jan 2020.

Vancouver:

Gozalbo Rovira RV. Hacia la caracterización del epítopo del autoantígeno en el Síndrome de Goodpasture . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2014. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10550/40335.

Council of Science Editors:

Gozalbo Rovira RV. Hacia la caracterización del epítopo del autoantígeno en el Síndrome de Goodpasture . [Doctoral Dissertation]. Universitat de Valencia; 2014. Available from: http://hdl.handle.net/10550/40335


University of Arizona

13. Lamba, Vandana. Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display .

Degree: 2012, University of Arizona

 Protein kinases function as key regulators in a variety of signaling pathways by executing the phosphorylation of a variety of protein substrates. Perturbation in the… (more)

Subjects/Keywords: Protein Kinases; Chemistry; Bivalent Inhibitors; Phage Display

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APA (6th Edition):

Lamba, V. (2012). Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/265559

Chicago Manual of Style (16th Edition):

Lamba, Vandana. “Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display .” 2012. Doctoral Dissertation, University of Arizona. Accessed January 22, 2020. http://hdl.handle.net/10150/265559.

MLA Handbook (7th Edition):

Lamba, Vandana. “Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display .” 2012. Web. 22 Jan 2020.

Vancouver:

Lamba V. Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10150/265559.

Council of Science Editors:

Lamba V. Development of Potent and Selective Bivalent Inhibitors for Protein Kinases Utilizing Phage Display . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/265559


University of Ottawa

14. Keklikian, Artine. Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library .

Degree: 2011, University of Ottawa

 Antibody phage display technology mimics the natural immune system, and has been widely used for rapid isolation of single-domain antibodies (sdAbs) with various binding specificities… (more)

Subjects/Keywords: Antibody phage display; Single domain antibody; VL

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APA (6th Edition):

Keklikian, A. (2011). Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/20197

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):

Keklikian, Artine. “Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library .” 2011. Thesis, University of Ottawa. Accessed January 22, 2020. http://hdl.handle.net/10393/20197.

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

MLA Handbook (7th Edition):

Keklikian, Artine. “Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library .” 2011. Web. 22 Jan 2020.

Vancouver:

Keklikian A. Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10393/20197.

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

Council of Science Editors:

Keklikian A. Construction of a Synthetic Human VL Phage Display Library and Isolation of Potential Neuropilin-1-specific VL Therapeutics from the Library . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/20197

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


University of Illinois – Chicago

15. Gorman, Kevin Thomas. Designer Affinity Reagents for Biomarker Detection.

Degree: 2017, University of Illinois – Chicago

 Biomarkers are molecules whose presence is indicative of some biological phenomena, such as disease or infection. Since their discovery, biomarkers have played a vital role… (more)

Subjects/Keywords: phage-display; affinity reagents; sandwich assay

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APA (6th Edition):

Gorman, K. T. (2017). Designer Affinity Reagents for Biomarker Detection. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21956

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):

Gorman, Kevin Thomas. “Designer Affinity Reagents for Biomarker Detection.” 2017. Thesis, University of Illinois – Chicago. Accessed January 22, 2020. http://hdl.handle.net/10027/21956.

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

MLA Handbook (7th Edition):

Gorman, Kevin Thomas. “Designer Affinity Reagents for Biomarker Detection.” 2017. Web. 22 Jan 2020.

Vancouver:

Gorman KT. Designer Affinity Reagents for Biomarker Detection. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10027/21956.

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

Council of Science Editors:

Gorman KT. Designer Affinity Reagents for Biomarker Detection. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/21956

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


Georgia Tech

16. Moretti, Leandro. Approaches to improve expression and specificity of an antibody probe against fibronectin.

Degree: MS, Mechanical Engineering, 2016, Georgia Tech

Phage display is a convenient method to select proteins of interest based on binding affinity. The Barker lab recently used this technology to discover an… (more)

Subjects/Keywords: Fibrosis; scFv; Phage display; Antibody fragment; Antibody

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APA (6th Edition):

Moretti, L. (2016). Approaches to improve expression and specificity of an antibody probe against fibronectin. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59115

Chicago Manual of Style (16th Edition):

Moretti, Leandro. “Approaches to improve expression and specificity of an antibody probe against fibronectin.” 2016. Masters Thesis, Georgia Tech. Accessed January 22, 2020. http://hdl.handle.net/1853/59115.

MLA Handbook (7th Edition):

Moretti, Leandro. “Approaches to improve expression and specificity of an antibody probe against fibronectin.” 2016. Web. 22 Jan 2020.

Vancouver:

Moretti L. Approaches to improve expression and specificity of an antibody probe against fibronectin. [Internet] [Masters thesis]. Georgia Tech; 2016. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/1853/59115.

Council of Science Editors:

Moretti L. Approaches to improve expression and specificity of an antibody probe against fibronectin. [Masters Thesis]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59115


Iowa State University

17. Williams, Jeffrey. Development of a phage display library for discovery of antigenic Brucella peptides.

Degree: 2018, Iowa State University

 Current serological diagnostics of the zoonotic disease brucellosis, caused by the intracellular, facultative bacterial pathogen Brucella, is primarily limited to humoral antibodies against the O-side… (more)

Subjects/Keywords: antigen; Brucella; phage display library; Microbiology

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APA (6th Edition):

Williams, J. (2018). Development of a phage display library for discovery of antigenic Brucella peptides. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16896

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):

Williams, Jeffrey. “Development of a phage display library for discovery of antigenic Brucella peptides.” 2018. Thesis, Iowa State University. Accessed January 22, 2020. https://lib.dr.iastate.edu/etd/16896.

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

MLA Handbook (7th Edition):

Williams, Jeffrey. “Development of a phage display library for discovery of antigenic Brucella peptides.” 2018. Web. 22 Jan 2020.

Vancouver:

Williams J. Development of a phage display library for discovery of antigenic Brucella peptides. [Internet] [Thesis]. Iowa State University; 2018. [cited 2020 Jan 22]. Available from: https://lib.dr.iastate.edu/etd/16896.

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

Council of Science Editors:

Williams J. Development of a phage display library for discovery of antigenic Brucella peptides. [Thesis]. Iowa State University; 2018. Available from: https://lib.dr.iastate.edu/etd/16896

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

18. Gomes, Carlos Henrique Rodrigues. Construção de uma bibilioteca de anticorpos ScFv dirigidos contra o fator de crescimento vascular (VEGF).

Degree: Mestrado, Bioquímica, 2013, University of São Paulo

Angiogênese é a formação de novos vasos sanguíneos a partir de vasos já existentes e é importante em processos fisiológicos, que em adultos é restrita… (more)

Subjects/Keywords: Anticorpos monoclonais; Biotechnology; Biotecnologia; Monoclonal antibodies; Phage display; Phage display; VEGF; VEGF

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

APA (6th Edition):

Gomes, C. H. R. (2013). Construção de uma bibilioteca de anticorpos ScFv dirigidos contra o fator de crescimento vascular (VEGF). (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-09082013-093807/ ;

Chicago Manual of Style (16th Edition):

Gomes, Carlos Henrique Rodrigues. “Construção de uma bibilioteca de anticorpos ScFv dirigidos contra o fator de crescimento vascular (VEGF).” 2013. Masters Thesis, University of São Paulo. Accessed January 22, 2020. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-09082013-093807/ ;.

MLA Handbook (7th Edition):

Gomes, Carlos Henrique Rodrigues. “Construção de uma bibilioteca de anticorpos ScFv dirigidos contra o fator de crescimento vascular (VEGF).” 2013. Web. 22 Jan 2020.

Vancouver:

Gomes CHR. Construção de uma bibilioteca de anticorpos ScFv dirigidos contra o fator de crescimento vascular (VEGF). [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2020 Jan 22]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-09082013-093807/ ;.

Council of Science Editors:

Gomes CHR. Construção de uma bibilioteca de anticorpos ScFv dirigidos contra o fator de crescimento vascular (VEGF). [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-09082013-093807/ ;

19. Lima, Swiany Silveira. Identificação de adesinas de Leptospira interrogans por shotgun phage display.

Degree: PhD, Bioquímica, 2013, University of São Paulo

Em Leptospira interrogans algumas proteínas com capacidade de ligação aos componentes de matriz extracelular foram identificadas e, em sua maioria, são fatores de virulência. Phage(more)

Subjects/Keywords: Adesina; Adhesin; Leptospira interrogans; Leptospira interrogans; Shotgun phage display; Shotgun phage display; Vaccine; Vacinas

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APA (6th Edition):

Lima, S. S. (2013). Identificação de adesinas de Leptospira interrogans por shotgun phage display. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-02052013-095417/ ;

Chicago Manual of Style (16th Edition):

Lima, Swiany Silveira. “Identificação de adesinas de Leptospira interrogans por shotgun phage display.” 2013. Doctoral Dissertation, University of São Paulo. Accessed January 22, 2020. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-02052013-095417/ ;.

MLA Handbook (7th Edition):

Lima, Swiany Silveira. “Identificação de adesinas de Leptospira interrogans por shotgun phage display.” 2013. Web. 22 Jan 2020.

Vancouver:

Lima SS. Identificação de adesinas de Leptospira interrogans por shotgun phage display. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2020 Jan 22]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-02052013-095417/ ;.

Council of Science Editors:

Lima SS. Identificação de adesinas de Leptospira interrogans por shotgun phage display. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-02052013-095417/ ;

20. Galber Rodrigues Araujo. Isolamento e identificação de mimetopos de auto-antígenos para utilização em imunodiagnóstico da artrite idiopática juvenil.

Degree: 2011, Federal University of Uberlândia

 CAPITULO 1: A Artrite Idiopática Juvenil (AIJ) é uma doença auto-imune caracterizada por artrite persistente, de causa desconhecida, que se inicia antes dos 16 anos… (more)

Subjects/Keywords: Phage Display; Marcadores sorológicos; Artrite idiopática juvenil; Imunodiagnóstico; GENETICA; Juvenile Idiopathic Arthritis; Phage Display; Immunodiagnostic

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APA (6th Edition):

Araujo, G. R. (2011). Isolamento e identificação de mimetopos de auto-antígenos para utilização em imunodiagnóstico da artrite idiopática juvenil. (Thesis). Federal University of Uberlândia. Retrieved from http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=3751

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):

Araujo, Galber Rodrigues. “Isolamento e identificação de mimetopos de auto-antígenos para utilização em imunodiagnóstico da artrite idiopática juvenil.” 2011. Thesis, Federal University of Uberlândia. Accessed January 22, 2020. http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=3751.

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

MLA Handbook (7th Edition):

Araujo, Galber Rodrigues. “Isolamento e identificação de mimetopos de auto-antígenos para utilização em imunodiagnóstico da artrite idiopática juvenil.” 2011. Web. 22 Jan 2020.

Vancouver:

Araujo GR. Isolamento e identificação de mimetopos de auto-antígenos para utilização em imunodiagnóstico da artrite idiopática juvenil. [Internet] [Thesis]. Federal University of Uberlândia; 2011. [cited 2020 Jan 22]. Available from: http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=3751.

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

Council of Science Editors:

Araujo GR. Isolamento e identificação de mimetopos de auto-antígenos para utilização em imunodiagnóstico da artrite idiopática juvenil. [Thesis]. Federal University of Uberlândia; 2011. Available from: http://www.bdtd.ufu.br//tde_busca/arquivo.php?codArquivo=3751

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

21. Muller, Benjamin. Création d'une banque de scFv-phages ciblant des protéines hydrophiles ou membranaires : Creation of a new scFv-phage library targeting hydrophilic or membrane proteins.

Degree: Docteur es, Biologie Santé, 2014, Université Montpellier I

Actuellement, 60% des médicaments sur le marché ont pour cible des protéines membranaires. Toutefois, l'étude de ces protéines membranaires reste un challenge de par leur… (more)

Subjects/Keywords: Anticorps monoclonaux; Exosomes; Phage display; Hybridomes; Monoclonal antibodies; Exosomes; Phage display; Hybridoma; 615

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APA (6th Edition):

Muller, B. (2014). Création d'une banque de scFv-phages ciblant des protéines hydrophiles ou membranaires : Creation of a new scFv-phage library targeting hydrophilic or membrane proteins. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2014MON13511

Chicago Manual of Style (16th Edition):

Muller, Benjamin. “Création d'une banque de scFv-phages ciblant des protéines hydrophiles ou membranaires : Creation of a new scFv-phage library targeting hydrophilic or membrane proteins.” 2014. Doctoral Dissertation, Université Montpellier I. Accessed January 22, 2020. http://www.theses.fr/2014MON13511.

MLA Handbook (7th Edition):

Muller, Benjamin. “Création d'une banque de scFv-phages ciblant des protéines hydrophiles ou membranaires : Creation of a new scFv-phage library targeting hydrophilic or membrane proteins.” 2014. Web. 22 Jan 2020.

Vancouver:

Muller B. Création d'une banque de scFv-phages ciblant des protéines hydrophiles ou membranaires : Creation of a new scFv-phage library targeting hydrophilic or membrane proteins. [Internet] [Doctoral dissertation]. Université Montpellier I; 2014. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2014MON13511.

Council of Science Editors:

Muller B. Création d'une banque de scFv-phages ciblant des protéines hydrophiles ou membranaires : Creation of a new scFv-phage library targeting hydrophilic or membrane proteins. [Doctoral Dissertation]. Université Montpellier I; 2014. Available from: http://www.theses.fr/2014MON13511


Université Paris-Sud – Paris XI

22. Joulie, Michaël. Recherche de nouvelles protéines humaines se liant à l'ADN méthylé : Investigation for new human metyl-CpG-binding proteins.

Degree: Docteur es, Biologie, 2011, Université Paris-Sud – Paris XI

L'épigénétique est un composant essentiel du fonctionnement des génomes eucaryotes. Les divers phénomènes épigénétiques modifient l’état chromatinien et participent à la plasticité du génome, mais… (more)

Subjects/Keywords: Épigénétique; Méthylation de l’ADN; MBP; Phage display; Epigenetics; DNA methylation; Methyl binding proteins; Phage display

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APA (6th Edition):

Joulie, M. (2011). Recherche de nouvelles protéines humaines se liant à l'ADN méthylé : Investigation for new human metyl-CpG-binding proteins. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA112157

Chicago Manual of Style (16th Edition):

Joulie, Michaël. “Recherche de nouvelles protéines humaines se liant à l'ADN méthylé : Investigation for new human metyl-CpG-binding proteins.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 22, 2020. http://www.theses.fr/2011PA112157.

MLA Handbook (7th Edition):

Joulie, Michaël. “Recherche de nouvelles protéines humaines se liant à l'ADN méthylé : Investigation for new human metyl-CpG-binding proteins.” 2011. Web. 22 Jan 2020.

Vancouver:

Joulie M. Recherche de nouvelles protéines humaines se liant à l'ADN méthylé : Investigation for new human metyl-CpG-binding proteins. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2011PA112157.

Council of Science Editors:

Joulie M. Recherche de nouvelles protéines humaines se liant à l'ADN méthylé : Investigation for new human metyl-CpG-binding proteins. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA112157

23. Murarasu, Thomas. The Shiga Toxin B-Subunit : a Promising Scaffold for the Targeting of Tumor Specific Glycosphingolipids : Exploitation de l’échafaudage moléculaire de la sous-unité B de la Toxine de Shiga pour le ciblage des glycosphingolipides tumoraux.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Paris Saclay

Le cancer représente la second cause de décès au monde. Le développement de traitements innovants contre le cancer repose aujourd’hui sur l’identification de biomarqueurs des… (more)

Subjects/Keywords: Lectine synthétique; Phage display; Ciblage tumorale; Synthetic lectins; Phage display; Tumor targeting

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APA (6th Edition):

Murarasu, T. (2017). The Shiga Toxin B-Subunit : a Promising Scaffold for the Targeting of Tumor Specific Glycosphingolipids : Exploitation de l’échafaudage moléculaire de la sous-unité B de la Toxine de Shiga pour le ciblage des glycosphingolipides tumoraux. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLS512

Chicago Manual of Style (16th Edition):

Murarasu, Thomas. “The Shiga Toxin B-Subunit : a Promising Scaffold for the Targeting of Tumor Specific Glycosphingolipids : Exploitation de l’échafaudage moléculaire de la sous-unité B de la Toxine de Shiga pour le ciblage des glycosphingolipides tumoraux.” 2017. Doctoral Dissertation, Paris Saclay. Accessed January 22, 2020. http://www.theses.fr/2017SACLS512.

MLA Handbook (7th Edition):

Murarasu, Thomas. “The Shiga Toxin B-Subunit : a Promising Scaffold for the Targeting of Tumor Specific Glycosphingolipids : Exploitation de l’échafaudage moléculaire de la sous-unité B de la Toxine de Shiga pour le ciblage des glycosphingolipides tumoraux.” 2017. Web. 22 Jan 2020.

Vancouver:

Murarasu T. The Shiga Toxin B-Subunit : a Promising Scaffold for the Targeting of Tumor Specific Glycosphingolipids : Exploitation de l’échafaudage moléculaire de la sous-unité B de la Toxine de Shiga pour le ciblage des glycosphingolipides tumoraux. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2017SACLS512.

Council of Science Editors:

Murarasu T. The Shiga Toxin B-Subunit : a Promising Scaffold for the Targeting of Tumor Specific Glycosphingolipids : Exploitation de l’échafaudage moléculaire de la sous-unité B de la Toxine de Shiga pour le ciblage des glycosphingolipides tumoraux. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLS512


University of New Mexico

24. Jordan, Sheldon Keith. Engineering RNA phage MS2 virus-like particles for peptide display.

Degree: Biomedical Sciences Graduate Program, 2010, University of New Mexico

Phage display is a powerful and versatile technology that enables the selection of novel binding functions from large populations of randomly generated peptide sequences. Random… (more)

Subjects/Keywords: bacteriophage MS2; virus-like particle; nanoscience; biomedical engineering; phage display; phage vaccine

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APA (6th Edition):

Jordan, S. K. (2010). Engineering RNA phage MS2 virus-like particles for peptide display. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/13

Chicago Manual of Style (16th Edition):

Jordan, Sheldon Keith. “Engineering RNA phage MS2 virus-like particles for peptide display.” 2010. Doctoral Dissertation, University of New Mexico. Accessed January 22, 2020. https://digitalrepository.unm.edu/biom_etds/13.

MLA Handbook (7th Edition):

Jordan, Sheldon Keith. “Engineering RNA phage MS2 virus-like particles for peptide display.” 2010. Web. 22 Jan 2020.

Vancouver:

Jordan SK. Engineering RNA phage MS2 virus-like particles for peptide display. [Internet] [Doctoral dissertation]. University of New Mexico; 2010. [cited 2020 Jan 22]. Available from: https://digitalrepository.unm.edu/biom_etds/13.

Council of Science Editors:

Jordan SK. Engineering RNA phage MS2 virus-like particles for peptide display. [Doctoral Dissertation]. University of New Mexico; 2010. Available from: https://digitalrepository.unm.edu/biom_etds/13

25. Lamort, Anne-Sophie. Etude fonctionnelle de la MMp - 12 de macrophage en vue de son ciblage thérapeutique dans la broncho-pneumopathie chronique obstructive : Functional study of macrophage MMp-12 in order to its therapeutic targeting in chronic obstructive pulmonary disease.

Degree: Docteur es, Sciences de la vie, spécialité Biochimie, 2015, Université François-Rabelais de Tours

La bronchopneumopathie chronique obstructive ou BPCO est une atteinte des voies respiratoires causée par le tabagisme. Cette maladie pulmonaire chronique et non réversible pour laquelle… (more)

Subjects/Keywords: Protéase; MMP-12; BPCO; Substrats fluorogéniques; Anticorps; "scFv"; Phage display; Protease; MMP-12; COPD; Fluorogenic substrates; Antibody; "scFv"; Phage display

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APA (6th Edition):

Lamort, A. (2015). Etude fonctionnelle de la MMp - 12 de macrophage en vue de son ciblage thérapeutique dans la broncho-pneumopathie chronique obstructive : Functional study of macrophage MMp-12 in order to its therapeutic targeting in chronic obstructive pulmonary disease. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2015TOUR4043

Chicago Manual of Style (16th Edition):

Lamort, Anne-Sophie. “Etude fonctionnelle de la MMp - 12 de macrophage en vue de son ciblage thérapeutique dans la broncho-pneumopathie chronique obstructive : Functional study of macrophage MMp-12 in order to its therapeutic targeting in chronic obstructive pulmonary disease.” 2015. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed January 22, 2020. http://www.theses.fr/2015TOUR4043.

MLA Handbook (7th Edition):

Lamort, Anne-Sophie. “Etude fonctionnelle de la MMp - 12 de macrophage en vue de son ciblage thérapeutique dans la broncho-pneumopathie chronique obstructive : Functional study of macrophage MMp-12 in order to its therapeutic targeting in chronic obstructive pulmonary disease.” 2015. Web. 22 Jan 2020.

Vancouver:

Lamort A. Etude fonctionnelle de la MMp - 12 de macrophage en vue de son ciblage thérapeutique dans la broncho-pneumopathie chronique obstructive : Functional study of macrophage MMp-12 in order to its therapeutic targeting in chronic obstructive pulmonary disease. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2015. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2015TOUR4043.

Council of Science Editors:

Lamort A. Etude fonctionnelle de la MMp - 12 de macrophage en vue de son ciblage thérapeutique dans la broncho-pneumopathie chronique obstructive : Functional study of macrophage MMp-12 in order to its therapeutic targeting in chronic obstructive pulmonary disease. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2015. Available from: http://www.theses.fr/2015TOUR4043


Université de Grenoble

26. Chahboun, Siham. Comparaison des régions variables des anticorps de macaques (Macaca fascicularis) et de l' Homme et leurs utilisation pour la neutralisation des toxines botuliques A et B : Comparison of macaque (Macaca fascicularis)and human antibodies variable regions, and their use for botulinum toxins A and B neutralization.

Degree: Docteur es, Sciences de la vie, 2013, Université de Grenoble

Notre laboratoire a développé une stratégie d'isolement de fragments d'anticorps recombinants à partir de primates non humains (Macaca fascicularis) immunisés, en utilisant la technologie des… (more)

Subjects/Keywords: Anticorps; Phage display; Humanisation; Neutralisation; Primate non humain; Toxines; Antibody; Phage display; Toxin; Humanization; Neutralization; Non human primate

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APA (6th Edition):

Chahboun, S. (2013). Comparaison des régions variables des anticorps de macaques (Macaca fascicularis) et de l' Homme et leurs utilisation pour la neutralisation des toxines botuliques A et B : Comparison of macaque (Macaca fascicularis)and human antibodies variable regions, and their use for botulinum toxins A and B neutralization. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENV022

Chicago Manual of Style (16th Edition):

Chahboun, Siham. “Comparaison des régions variables des anticorps de macaques (Macaca fascicularis) et de l' Homme et leurs utilisation pour la neutralisation des toxines botuliques A et B : Comparison of macaque (Macaca fascicularis)and human antibodies variable regions, and their use for botulinum toxins A and B neutralization.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed January 22, 2020. http://www.theses.fr/2013GRENV022.

MLA Handbook (7th Edition):

Chahboun, Siham. “Comparaison des régions variables des anticorps de macaques (Macaca fascicularis) et de l' Homme et leurs utilisation pour la neutralisation des toxines botuliques A et B : Comparison of macaque (Macaca fascicularis)and human antibodies variable regions, and their use for botulinum toxins A and B neutralization.” 2013. Web. 22 Jan 2020.

Vancouver:

Chahboun S. Comparaison des régions variables des anticorps de macaques (Macaca fascicularis) et de l' Homme et leurs utilisation pour la neutralisation des toxines botuliques A et B : Comparison of macaque (Macaca fascicularis)and human antibodies variable regions, and their use for botulinum toxins A and B neutralization. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2013GRENV022.

Council of Science Editors:

Chahboun S. Comparaison des régions variables des anticorps de macaques (Macaca fascicularis) et de l' Homme et leurs utilisation pour la neutralisation des toxines botuliques A et B : Comparison of macaque (Macaca fascicularis)and human antibodies variable regions, and their use for botulinum toxins A and B neutralization. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENV022

27. Érika Seki Kioshima. Caracterização de marcadores de virulência em Paracoccidioides brasiliensis.

Degree: 2009, Universidade Federal de São Paulo

A paracoccidioidomicose (PCM) é uma doença sistêmica de caráter granulomatoso, prevalente na América do Sul, causada pelo fungo termodimórfico Paracoccidioides brasiliensis. O fungo apresenta estrutura… (more)

Subjects/Keywords: 1. Paracoccidiodes brasiliensis 2. Virulência 3. Peptídeos 4. Phage display 5. Biomarcador; MICROBIOLOGIA; 1. Paracoccidiodes brasiliensis 2. Phage display

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APA (6th Edition):

Kioshima, . S. (2009). Caracterização de marcadores de virulência em Paracoccidioides brasiliensis. (Thesis). Universidade Federal de São Paulo. Retrieved from http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=387 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=388

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):

Kioshima, Érika Seki. “Caracterização de marcadores de virulência em Paracoccidioides brasiliensis.” 2009. Thesis, Universidade Federal de São Paulo. Accessed January 22, 2020. http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=387 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=388.

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

MLA Handbook (7th Edition):

Kioshima, Érika Seki. “Caracterização de marcadores de virulência em Paracoccidioides brasiliensis.” 2009. Web. 22 Jan 2020.

Vancouver:

Kioshima S. Caracterização de marcadores de virulência em Paracoccidioides brasiliensis. [Internet] [Thesis]. Universidade Federal de São Paulo; 2009. [cited 2020 Jan 22]. Available from: http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=387 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=388.

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

Council of Science Editors:

Kioshima S. Caracterização de marcadores de virulência em Paracoccidioides brasiliensis. [Thesis]. Universidade Federal de São Paulo; 2009. Available from: http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=387 ; http://www.bdtd.unifesp.br/tede//tde_busca/arquivo.php?codArquivo=388

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

28. Nevoltris, Damien. Développement des ligands pour l' étude des récepteurs GPCR, Tyrosine Kinase, basée sur l' utilisation de simple domaine d' anticorps de lamas : Study of G protein-coupled receptor (GPCR), tyrosine kinase (RTK) and ion channels by using llama antibodies (Nanobody).

Degree: Docteur es, Immunologie, 2014, Aix Marseille Université

La recherche de nouvelles molécules à visée thérapeutique ou diagnostic ciblant les récepteurs membranaires incluant les RCPGs, les récepteurs à tyrosine kinase et les canaux… (more)

Subjects/Keywords: Anticorps à domaine unique; Phage display; Fret; ErbBs; MGluRs; Single domain antibodies; Phage display; Fret; ErbBs; MGluRs; 571

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APA (6th Edition):

Nevoltris, D. (2014). Développement des ligands pour l' étude des récepteurs GPCR, Tyrosine Kinase, basée sur l' utilisation de simple domaine d' anticorps de lamas : Study of G protein-coupled receptor (GPCR), tyrosine kinase (RTK) and ion channels by using llama antibodies (Nanobody). (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4063

Chicago Manual of Style (16th Edition):

Nevoltris, Damien. “Développement des ligands pour l' étude des récepteurs GPCR, Tyrosine Kinase, basée sur l' utilisation de simple domaine d' anticorps de lamas : Study of G protein-coupled receptor (GPCR), tyrosine kinase (RTK) and ion channels by using llama antibodies (Nanobody).” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed January 22, 2020. http://www.theses.fr/2014AIXM4063.

MLA Handbook (7th Edition):

Nevoltris, Damien. “Développement des ligands pour l' étude des récepteurs GPCR, Tyrosine Kinase, basée sur l' utilisation de simple domaine d' anticorps de lamas : Study of G protein-coupled receptor (GPCR), tyrosine kinase (RTK) and ion channels by using llama antibodies (Nanobody).” 2014. Web. 22 Jan 2020.

Vancouver:

Nevoltris D. Développement des ligands pour l' étude des récepteurs GPCR, Tyrosine Kinase, basée sur l' utilisation de simple domaine d' anticorps de lamas : Study of G protein-coupled receptor (GPCR), tyrosine kinase (RTK) and ion channels by using llama antibodies (Nanobody). [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2014AIXM4063.

Council of Science Editors:

Nevoltris D. Développement des ligands pour l' étude des récepteurs GPCR, Tyrosine Kinase, basée sur l' utilisation de simple domaine d' anticorps de lamas : Study of G protein-coupled receptor (GPCR), tyrosine kinase (RTK) and ion channels by using llama antibodies (Nanobody). [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4063

29. Rimbault, Charlotte. Modulation des interactions impliquant les domaines PDZ par une approche d’évolution dirigée : Modulation of PDZ domain-mediated interactions by a directed molecular evolution approach.

Degree: Docteur es, Biochimie, 2016, Bordeaux

Les interactions protéine-protéine (IPPs), complexes et dynamiques, sont le cœur des réseaux protéiques cellulaires. Au niveau des synapses excitatrices, la densité post-synaptique (PSD) est un… (more)

Subjects/Keywords: PSD95; Domaines PDZ; Évolution dirigée; Phage display; Interactions protéine-protéine; PSD95; PDZ domains; Directed evolution; Phage display; Protein-protein interactions

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

APA (6th Edition):

Rimbault, C. (2016). Modulation des interactions impliquant les domaines PDZ par une approche d’évolution dirigée : Modulation of PDZ domain-mediated interactions by a directed molecular evolution approach. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2016BORD0438

Chicago Manual of Style (16th Edition):

Rimbault, Charlotte. “Modulation des interactions impliquant les domaines PDZ par une approche d’évolution dirigée : Modulation of PDZ domain-mediated interactions by a directed molecular evolution approach.” 2016. Doctoral Dissertation, Bordeaux. Accessed January 22, 2020. http://www.theses.fr/2016BORD0438.

MLA Handbook (7th Edition):

Rimbault, Charlotte. “Modulation des interactions impliquant les domaines PDZ par une approche d’évolution dirigée : Modulation of PDZ domain-mediated interactions by a directed molecular evolution approach.” 2016. Web. 22 Jan 2020.

Vancouver:

Rimbault C. Modulation des interactions impliquant les domaines PDZ par une approche d’évolution dirigée : Modulation of PDZ domain-mediated interactions by a directed molecular evolution approach. [Internet] [Doctoral dissertation]. Bordeaux; 2016. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2016BORD0438.

Council of Science Editors:

Rimbault C. Modulation des interactions impliquant les domaines PDZ par une approche d’évolution dirigée : Modulation of PDZ domain-mediated interactions by a directed molecular evolution approach. [Doctoral Dissertation]. Bordeaux; 2016. Available from: http://www.theses.fr/2016BORD0438

30. Even, Klervi. Développement d' outils innovants pour le diagnostic et la découverte de cibles dans le cancer du sein : Rock and Literature : listening to a Contemporary Literary Field : noises, Distortions, Resonances.

Degree: Docteur es, Immunologie, 2012, Aix Marseille Université

Au cours de sa vie, 1 femme sur 9 sera atteinte du cancer du sein, 1 sur 27 sera emportée par cette maladie et 10… (more)

Subjects/Keywords: Anticorps simple domaine; Phage display; Marqueur; Cancer; Diagnostic; Single domain antibody; Phage display; Marker; Cancer; Diagnosis

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

APA (6th Edition):

Even, K. (2012). Développement d' outils innovants pour le diagnostic et la découverte de cibles dans le cancer du sein : Rock and Literature : listening to a Contemporary Literary Field : noises, Distortions, Resonances. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2012AIXM4019

Chicago Manual of Style (16th Edition):

Even, Klervi. “Développement d' outils innovants pour le diagnostic et la découverte de cibles dans le cancer du sein : Rock and Literature : listening to a Contemporary Literary Field : noises, Distortions, Resonances.” 2012. Doctoral Dissertation, Aix Marseille Université. Accessed January 22, 2020. http://www.theses.fr/2012AIXM4019.

MLA Handbook (7th Edition):

Even, Klervi. “Développement d' outils innovants pour le diagnostic et la découverte de cibles dans le cancer du sein : Rock and Literature : listening to a Contemporary Literary Field : noises, Distortions, Resonances.” 2012. Web. 22 Jan 2020.

Vancouver:

Even K. Développement d' outils innovants pour le diagnostic et la découverte de cibles dans le cancer du sein : Rock and Literature : listening to a Contemporary Literary Field : noises, Distortions, Resonances. [Internet] [Doctoral dissertation]. Aix Marseille Université 2012. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2012AIXM4019.

Council of Science Editors:

Even K. Développement d' outils innovants pour le diagnostic et la découverte de cibles dans le cancer du sein : Rock and Literature : listening to a Contemporary Literary Field : noises, Distortions, Resonances. [Doctoral Dissertation]. Aix Marseille Université 2012. Available from: http://www.theses.fr/2012AIXM4019

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