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You searched for subject:(Yeast Surface Display). Showing records 1 – 14 of 14 total matches.

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1. Pauthenier, Cyrille. Développement d’une nouvelle méthodologie pour la production de molécules par ingénierie métabolique en délocalisant tout ou partie des réactions enzymatiques sur la surface de S. cerevisiae : Development of a new methodology for molecular production via metabolic engineering by relocating all or part of the enzymatic reaction on the surface of S. cerevisiae.

Degree: Docteur es, Sciences de la vie et de la santé, 2016, Université Paris-Saclay (ComUE)

L’ingénierie métabolique est une discipline qui vise à modifier artificiellement le métabolisme d’un organisme afin de lui faire produire un composé chimique d’intérêt. L’une des… (more)

Subjects/Keywords: Yeast surface display

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

APA (6th Edition):

Pauthenier, C. (2016). Développement d’une nouvelle méthodologie pour la production de molécules par ingénierie métabolique en délocalisant tout ou partie des réactions enzymatiques sur la surface de S. cerevisiae : Development of a new methodology for molecular production via metabolic engineering by relocating all or part of the enzymatic reaction on the surface of S. cerevisiae. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLE029

Chicago Manual of Style (16th Edition):

Pauthenier, Cyrille. “Développement d’une nouvelle méthodologie pour la production de molécules par ingénierie métabolique en délocalisant tout ou partie des réactions enzymatiques sur la surface de S. cerevisiae : Development of a new methodology for molecular production via metabolic engineering by relocating all or part of the enzymatic reaction on the surface of S. cerevisiae.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed March 04, 2021. http://www.theses.fr/2016SACLE029.

MLA Handbook (7th Edition):

Pauthenier, Cyrille. “Développement d’une nouvelle méthodologie pour la production de molécules par ingénierie métabolique en délocalisant tout ou partie des réactions enzymatiques sur la surface de S. cerevisiae : Development of a new methodology for molecular production via metabolic engineering by relocating all or part of the enzymatic reaction on the surface of S. cerevisiae.” 2016. Web. 04 Mar 2021.

Vancouver:

Pauthenier C. Développement d’une nouvelle méthodologie pour la production de molécules par ingénierie métabolique en délocalisant tout ou partie des réactions enzymatiques sur la surface de S. cerevisiae : Development of a new methodology for molecular production via metabolic engineering by relocating all or part of the enzymatic reaction on the surface of S. cerevisiae. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2021 Mar 04]. Available from: http://www.theses.fr/2016SACLE029.

Council of Science Editors:

Pauthenier C. Développement d’une nouvelle méthodologie pour la production de molécules par ingénierie métabolique en délocalisant tout ou partie des réactions enzymatiques sur la surface de S. cerevisiae : Development of a new methodology for molecular production via metabolic engineering by relocating all or part of the enzymatic reaction on the surface of S. cerevisiae. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLE029


Cornell University

2. Meng, Hsien-Wei. Development Of Dna Aptamers By Cell-Selex Using Yeast Cell Surface Display.

Degree: PhD, Veterinary Medicine, 2014, Cornell University

 SELEX, the process of selecting aptamers, is often hampered by the difficulty of preparing target molecules in their native forms and by a lack of… (more)

Subjects/Keywords: Aptamer; Cell-SELEX; Yeast Surface Display

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APA (6th Edition):

Meng, H. (2014). Development Of Dna Aptamers By Cell-Selex Using Yeast Cell Surface Display. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36083

Chicago Manual of Style (16th Edition):

Meng, Hsien-Wei. “Development Of Dna Aptamers By Cell-Selex Using Yeast Cell Surface Display.” 2014. Doctoral Dissertation, Cornell University. Accessed March 04, 2021. http://hdl.handle.net/1813/36083.

MLA Handbook (7th Edition):

Meng, Hsien-Wei. “Development Of Dna Aptamers By Cell-Selex Using Yeast Cell Surface Display.” 2014. Web. 04 Mar 2021.

Vancouver:

Meng H. Development Of Dna Aptamers By Cell-Selex Using Yeast Cell Surface Display. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/1813/36083.

Council of Science Editors:

Meng H. Development Of Dna Aptamers By Cell-Selex Using Yeast Cell Surface Display. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36083


University of Illinois – Urbana-Champaign

3. Yu, Yi. Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides.

Degree: PhD, Biochemistry, 2015, University of Illinois – Urbana-Champaign

 Lanthipeptides are natural products that belong to the family of ribosomally synthesized and posttranslationally modified peptides (RiPPs). They contain the characteristic lanthionine (Lan) or methyllanthionine… (more)

Subjects/Keywords: Lanthipeptide; Lanthionine synthetase; Yeast surface display

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APA (6th Edition):

Yu, Y. (2015). Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89191

Chicago Manual of Style (16th Edition):

Yu, Yi. “Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 04, 2021. http://hdl.handle.net/2142/89191.

MLA Handbook (7th Edition):

Yu, Yi. “Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides.” 2015. Web. 04 Mar 2021.

Vancouver:

Yu Y. Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/2142/89191.

Council of Science Editors:

Yu Y. Mechanistic studies of class II lanthipeptide synthetases and yeast surface display of lanthipeptide leader peptides. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89191


University of Arkansas

4. Masniuk, Iaryna. Yeast surface display of CD154.

Degree: MS, 2012, University of Arkansas

  The CD154 (CD40L) is a member of tumor necrosis factor (TNF) family that plays a crucial role in regulation of both cell-mediated and humoral… (more)

Subjects/Keywords: Biological sciences; CD154; Yeast surface display; Medical Cell Biology; Virus Diseases

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APA (6th Edition):

Masniuk, I. (2012). Yeast surface display of CD154. (Masters Thesis). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/438

Chicago Manual of Style (16th Edition):

Masniuk, Iaryna. “Yeast surface display of CD154.” 2012. Masters Thesis, University of Arkansas. Accessed March 04, 2021. https://scholarworks.uark.edu/etd/438.

MLA Handbook (7th Edition):

Masniuk, Iaryna. “Yeast surface display of CD154.” 2012. Web. 04 Mar 2021.

Vancouver:

Masniuk I. Yeast surface display of CD154. [Internet] [Masters thesis]. University of Arkansas; 2012. [cited 2021 Mar 04]. Available from: https://scholarworks.uark.edu/etd/438.

Council of Science Editors:

Masniuk I. Yeast surface display of CD154. [Masters Thesis]. University of Arkansas; 2012. Available from: https://scholarworks.uark.edu/etd/438


University of California – Riverside

5. Fang, Kuili. Development of a Flow-Cytometric Screening Method for MMP-14 Inhibitory Antibody.

Degree: Chemical and Environmental Engineering, 2014, University of California – Riverside

 Mounting evidence suggests that MMP-14 (Matrix Metalloproteinase-14) plays an important role in cancer proliferation, invasion and migration to other healthy tissues through its extracellular matrix… (more)

Subjects/Keywords: Chemical engineering; Biochemistry; Cancer therapy; FACS; inhibitory antibody; MMP-14; yeast surface display

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APA (6th Edition):

Fang, K. (2014). Development of a Flow-Cytometric Screening Method for MMP-14 Inhibitory Antibody. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/3xc162gb

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):

Fang, Kuili. “Development of a Flow-Cytometric Screening Method for MMP-14 Inhibitory Antibody.” 2014. Thesis, University of California – Riverside. Accessed March 04, 2021. http://www.escholarship.org/uc/item/3xc162gb.

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

MLA Handbook (7th Edition):

Fang, Kuili. “Development of a Flow-Cytometric Screening Method for MMP-14 Inhibitory Antibody.” 2014. Web. 04 Mar 2021.

Vancouver:

Fang K. Development of a Flow-Cytometric Screening Method for MMP-14 Inhibitory Antibody. [Internet] [Thesis]. University of California – Riverside; 2014. [cited 2021 Mar 04]. Available from: http://www.escholarship.org/uc/item/3xc162gb.

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

Council of Science Editors:

Fang K. Development of a Flow-Cytometric Screening Method for MMP-14 Inhibitory Antibody. [Thesis]. University of California – Riverside; 2014. Available from: http://www.escholarship.org/uc/item/3xc162gb

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


Univerzitet u Beogradu

6. Kovačević, Gordana N., 1987-. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.

Degree: Hemijski fakultet, 2019, Univerzitet u Beogradu

Hemija - Biohemija / Chemistry - Biochemistry

Glukoza-oksidaza (GOx) je vaţan industrijski enzim koji se predominantno koristi kao biokatalizator u industriji hrane za proizvodnju glukonske… (more)

Subjects/Keywords: glucose oxidase; high-throughput screening; oxidative stability; yeast surface display; green fluorescent protein; Pichia pastoris

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APA (6th Edition):

Kovačević, Gordana N., 1. (2019). Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get

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):

Kovačević, Gordana N., 1987-. “Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.” 2019. Thesis, Univerzitet u Beogradu. Accessed March 04, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get.

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

MLA Handbook (7th Edition):

Kovačević, Gordana N., 1987-. “Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.” 2019. Web. 04 Mar 2021.

Vancouver:

Kovačević, Gordana N. 1. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2021 Mar 04]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get.

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

Council of Science Editors:

Kovačević, Gordana N. 1. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get

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


University of Oxford

7. Alenazi, Yara. Targeting the chemokine signalling pathway using tick saliva peptides.

Degree: PhD, 2018, University of Oxford

 Chemokines are signalling proteins that function to recruit immune cells from the innate and adaptive immune response. Chemokines are classified based on the position of… (more)

Subjects/Keywords: Tick saliva; Evasin; Yeast surface display; Chemokine network; Chemokine; Inflammation; Chemokine binding protein

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APA (6th Edition):

Alenazi, Y. (2018). Targeting the chemokine signalling pathway using tick saliva peptides. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:76337925-4674-4181-9daa-235f74725241 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780518

Chicago Manual of Style (16th Edition):

Alenazi, Yara. “Targeting the chemokine signalling pathway using tick saliva peptides.” 2018. Doctoral Dissertation, University of Oxford. Accessed March 04, 2021. http://ora.ox.ac.uk/objects/uuid:76337925-4674-4181-9daa-235f74725241 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780518.

MLA Handbook (7th Edition):

Alenazi, Yara. “Targeting the chemokine signalling pathway using tick saliva peptides.” 2018. Web. 04 Mar 2021.

Vancouver:

Alenazi Y. Targeting the chemokine signalling pathway using tick saliva peptides. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2021 Mar 04]. Available from: http://ora.ox.ac.uk/objects/uuid:76337925-4674-4181-9daa-235f74725241 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780518.

Council of Science Editors:

Alenazi Y. Targeting the chemokine signalling pathway using tick saliva peptides. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:76337925-4674-4181-9daa-235f74725241 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780518


University of Tennessee – Knoxville

8. Price, James Vincent. A Tale of Two Protein Switches: Engineering, Characterizing, and Understanding a Novel and a Natural Switch.

Degree: 2013, University of Tennessee – Knoxville

 Throughout nature, many proteins provide a specific function in response to some input signal (e.g., phosyphorylation, pH, etc.), a process that is oftentimes described as… (more)

Subjects/Keywords: directed evolution; yeast surface display; hemagglutinin; I domain; Biochemical and Biomolecular Engineering

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APA (6th Edition):

Price, J. V. (2013). A Tale of Two Protein Switches: Engineering, Characterizing, and Understanding a Novel and a Natural Switch. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/2608

Chicago Manual of Style (16th Edition):

Price, James Vincent. “A Tale of Two Protein Switches: Engineering, Characterizing, and Understanding a Novel and a Natural Switch.” 2013. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed March 04, 2021. https://trace.tennessee.edu/utk_graddiss/2608.

MLA Handbook (7th Edition):

Price, James Vincent. “A Tale of Two Protein Switches: Engineering, Characterizing, and Understanding a Novel and a Natural Switch.” 2013. Web. 04 Mar 2021.

Vancouver:

Price JV. A Tale of Two Protein Switches: Engineering, Characterizing, and Understanding a Novel and a Natural Switch. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2013. [cited 2021 Mar 04]. Available from: https://trace.tennessee.edu/utk_graddiss/2608.

Council of Science Editors:

Price JV. A Tale of Two Protein Switches: Engineering, Characterizing, and Understanding a Novel and a Natural Switch. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2013. Available from: https://trace.tennessee.edu/utk_graddiss/2608


University of Minnesota

9. Chan, Jie Ying. Generation of engineered small protein scaffolds and insulin receptor targeting in human breast cancer.

Degree: PhD, Pharmacology, 2017, University of Minnesota

 The insulin-like growth factor (IGF) system is a well-studied growth regulatory pathway implicated in breast cancer tumorigenicity and drug resistance. The pivotal members of IGF… (more)

Subjects/Keywords: directed evolution; endocrine resistant breast cancer; T7 phage gene 2 protein; targeting insulin receptor; Yeast surface display

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APA (6th Edition):

Chan, J. Y. (2017). Generation of engineered small protein scaffolds and insulin receptor targeting in human breast cancer. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/188857

Chicago Manual of Style (16th Edition):

Chan, Jie Ying. “Generation of engineered small protein scaffolds and insulin receptor targeting in human breast cancer.” 2017. Doctoral Dissertation, University of Minnesota. Accessed March 04, 2021. http://hdl.handle.net/11299/188857.

MLA Handbook (7th Edition):

Chan, Jie Ying. “Generation of engineered small protein scaffolds and insulin receptor targeting in human breast cancer.” 2017. Web. 04 Mar 2021.

Vancouver:

Chan JY. Generation of engineered small protein scaffolds and insulin receptor targeting in human breast cancer. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/11299/188857.

Council of Science Editors:

Chan JY. Generation of engineered small protein scaffolds and insulin receptor targeting in human breast cancer. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/188857


University of Minnesota

10. Mikolajczyk, Brian. Protease Engineering To Enable Noninvasive Disease Detection.

Degree: PhD, Chemical Engineering, 2020, University of Minnesota

 Proteases are proteolytic enzymes with a wide range of industrial, biotechnological, and medical applications. Due to their importance, proteases have been the subject of many… (more)

Subjects/Keywords: enzyme engineering; fusion protein; library design; synthetic urinary reporter; tobacco etch virus protease; yeast surface display

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APA (6th Edition):

Mikolajczyk, B. (2020). Protease Engineering To Enable Noninvasive Disease Detection. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/215053

Chicago Manual of Style (16th Edition):

Mikolajczyk, Brian. “Protease Engineering To Enable Noninvasive Disease Detection.” 2020. Doctoral Dissertation, University of Minnesota. Accessed March 04, 2021. http://hdl.handle.net/11299/215053.

MLA Handbook (7th Edition):

Mikolajczyk, Brian. “Protease Engineering To Enable Noninvasive Disease Detection.” 2020. Web. 04 Mar 2021.

Vancouver:

Mikolajczyk B. Protease Engineering To Enable Noninvasive Disease Detection. [Internet] [Doctoral dissertation]. University of Minnesota; 2020. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/11299/215053.

Council of Science Editors:

Mikolajczyk B. Protease Engineering To Enable Noninvasive Disease Detection. [Doctoral Dissertation]. University of Minnesota; 2020. Available from: http://hdl.handle.net/11299/215053

11. Sivelle, Coline. Conception et production d’anticorps anti-TNFa non immunogènes pour le traitement des maladies inflammatoires : Conception and production of non-immunogenic anti-TNFa antibodies for inflammatory diseases treatment.

Degree: Docteur es, Immunologie, 2019, Université Paris-Saclay (ComUE)

L’efficacité des anticorps anti-TNFα peut être particulièrement affectée par leur immunogénicité. Elle se traduit par la production d’anticorps dirigés contre la protéine thérapeutique (ADA) et… (more)

Subjects/Keywords: Immunogénicité; Déimmunisation; Epitopes T; Adalimumab; Ingénierie des protéines; Expression à la surface de levure; Immunogenicity; Deimmunization; T-Celle epitopes; Adalimumab; Protein engineering; Yeast Surface Display

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APA (6th Edition):

Sivelle, C. (2019). Conception et production d’anticorps anti-TNFa non immunogènes pour le traitement des maladies inflammatoires : Conception and production of non-immunogenic anti-TNFa antibodies for inflammatory diseases treatment. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS603

Chicago Manual of Style (16th Edition):

Sivelle, Coline. “Conception et production d’anticorps anti-TNFa non immunogènes pour le traitement des maladies inflammatoires : Conception and production of non-immunogenic anti-TNFa antibodies for inflammatory diseases treatment.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed March 04, 2021. http://www.theses.fr/2019SACLS603.

MLA Handbook (7th Edition):

Sivelle, Coline. “Conception et production d’anticorps anti-TNFa non immunogènes pour le traitement des maladies inflammatoires : Conception and production of non-immunogenic anti-TNFa antibodies for inflammatory diseases treatment.” 2019. Web. 04 Mar 2021.

Vancouver:

Sivelle C. Conception et production d’anticorps anti-TNFa non immunogènes pour le traitement des maladies inflammatoires : Conception and production of non-immunogenic anti-TNFa antibodies for inflammatory diseases treatment. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2021 Mar 04]. Available from: http://www.theses.fr/2019SACLS603.

Council of Science Editors:

Sivelle C. Conception et production d’anticorps anti-TNFa non immunogènes pour le traitement des maladies inflammatoires : Conception and production of non-immunogenic anti-TNFa antibodies for inflammatory diseases treatment. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS603


University of Pennsylvania

12. Jiang, Wei. High-Throughput Engineering and Analysis of Class II Mhc/Peptide Binding by Yeast Co-Display.

Degree: 2010, University of Pennsylvania

 Polymorphisms of major histocompatibility complex (MHC) and molecular mechanisms of their antigen-presenting specificity and promiscuity have great impact on T cell-mediated immune responses and related… (more)

Subjects/Keywords: yeast surface display; MHC-II; directed evolution; peptide binding; yeast co-display; Biochemical and Biomolecular Engineering

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APA (6th Edition):

Jiang, W. (2010). High-Throughput Engineering and Analysis of Class II Mhc/Peptide Binding by Yeast Co-Display. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/419

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):

Jiang, Wei. “High-Throughput Engineering and Analysis of Class II Mhc/Peptide Binding by Yeast Co-Display.” 2010. Thesis, University of Pennsylvania. Accessed March 04, 2021. https://repository.upenn.edu/edissertations/419.

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

MLA Handbook (7th Edition):

Jiang, Wei. “High-Throughput Engineering and Analysis of Class II Mhc/Peptide Binding by Yeast Co-Display.” 2010. Web. 04 Mar 2021.

Vancouver:

Jiang W. High-Throughput Engineering and Analysis of Class II Mhc/Peptide Binding by Yeast Co-Display. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2021 Mar 04]. Available from: https://repository.upenn.edu/edissertations/419.

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

Council of Science Editors:

Jiang W. High-Throughput Engineering and Analysis of Class II Mhc/Peptide Binding by Yeast Co-Display. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/419

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

13. Tsai, Shen-Long. Artificial Cellulosomes and Arsenic Cleanup: From Single Cell Programming to Synthetic Yeast Consortium.

Degree: Chemical and Environmental Engineering, 2011, University of California – Riverside

 As our society marches toward a more technologically-inclined and industrialized future, energy and environmental sustainability are two of the most challenging problems we face today.… (more)

Subjects/Keywords: Chemical engineering; Arsenic; Cellulose; Cellulosome; Consortium; Surface display; Yeast

…intracellular expression, the level of secreted proteins is often impaired. 3 Yeast surface-display… …capability of yeast via cell surface-display of different cellulosomes was described in CHAPTER 2… …34 Figure 2.1. Functional assembly of minicellulosomes on the yeast cell surface… …Figure 3.4. Constitutive surface display of scaffoldin Scaf-ctf using the Agα1 anchor and the… …Figure 4.1. A schematic diagram of the complex cellulosome assembled on the yeast surface… 

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APA (6th Edition):

Tsai, S. (2011). Artificial Cellulosomes and Arsenic Cleanup: From Single Cell Programming to Synthetic Yeast Consortium. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/0fb629h4

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):

Tsai, Shen-Long. “Artificial Cellulosomes and Arsenic Cleanup: From Single Cell Programming to Synthetic Yeast Consortium.” 2011. Thesis, University of California – Riverside. Accessed March 04, 2021. http://www.escholarship.org/uc/item/0fb629h4.

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

MLA Handbook (7th Edition):

Tsai, Shen-Long. “Artificial Cellulosomes and Arsenic Cleanup: From Single Cell Programming to Synthetic Yeast Consortium.” 2011. Web. 04 Mar 2021.

Vancouver:

Tsai S. Artificial Cellulosomes and Arsenic Cleanup: From Single Cell Programming to Synthetic Yeast Consortium. [Internet] [Thesis]. University of California – Riverside; 2011. [cited 2021 Mar 04]. Available from: http://www.escholarship.org/uc/item/0fb629h4.

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

Council of Science Editors:

Tsai S. Artificial Cellulosomes and Arsenic Cleanup: From Single Cell Programming to Synthetic Yeast Consortium. [Thesis]. University of California – Riverside; 2011. Available from: http://www.escholarship.org/uc/item/0fb629h4

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


University of Illinois – Urbana-Champaign

14. Wen, Fei. Cell surface display in biomedical applications and biofuels production.

Degree: PhD, 0300, 2010, University of Illinois – Urbana-Champaign

 Cell surface display allows peptides or proteins to be expressed on the cell exterior as fusions to natural host anchoring motifs. It is a powerful… (more)

Subjects/Keywords: T cell; epitope; CD4+; Major histocompatibility complex (MHC); directed evolution; biofuel; Consolidated bioprocessing (CBP); yeast surface display; baculovirus display; affinity engineering; directed evolution; pMHC tetramer; cellulosome; minicellulosome; xylanosome; cellulase; hemicellulase

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

APA (6th Edition):

Wen, F. (2010). Cell surface display in biomedical applications and biofuels production. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15568

Chicago Manual of Style (16th Edition):

Wen, Fei. “Cell surface display in biomedical applications and biofuels production.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 04, 2021. http://hdl.handle.net/2142/15568.

MLA Handbook (7th Edition):

Wen, Fei. “Cell surface display in biomedical applications and biofuels production.” 2010. Web. 04 Mar 2021.

Vancouver:

Wen F. Cell surface display in biomedical applications and biofuels production. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2021 Mar 04]. Available from: http://hdl.handle.net/2142/15568.

Council of Science Editors:

Wen F. Cell surface display in biomedical applications and biofuels production. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15568

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