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You searched for subject:(Synthetic biology). Showing records 1 – 30 of 449 total matches.

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1. Tsarmpopoulos, Iason. Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools.

Degree: Docteur es, Microbiologie - immunologie, 2017, Bordeaux

Les mycoplasmes sont des bactéries pathogènes, dotées de petits génomes d’environ 1Mbp, avec une faible teneur en G+C. L'intérêt de la communauté scientifique pour ces… (more)

Subjects/Keywords: Biologie de synthèse; CRISPR/Cas9; Mycoplasma; Synthetic Biology; CRISPR/Cas9; Mycoplasma

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

APA (6th Edition):

Tsarmpopoulos, I. (2017). Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2017BORD0787

Chicago Manual of Style (16th Edition):

Tsarmpopoulos, Iason. “Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools.” 2017. Doctoral Dissertation, Bordeaux. Accessed May 25, 2019. http://www.theses.fr/2017BORD0787.

MLA Handbook (7th Edition):

Tsarmpopoulos, Iason. “Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools.” 2017. Web. 25 May 2019.

Vancouver:

Tsarmpopoulos I. Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools. [Internet] [Doctoral dissertation]. Bordeaux; 2017. [cited 2019 May 25]. Available from: http://www.theses.fr/2017BORD0787.

Council of Science Editors:

Tsarmpopoulos I. Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools. [Doctoral Dissertation]. Bordeaux; 2017. Available from: http://www.theses.fr/2017BORD0787

2. Guiziou, Sarah. Engineering framework for scalable recombinase logic operating in living cells : Développement d'un cadre systématique pour l'implémentation de logique dans les organismes vivants en utilisant les recombinases.

Degree: Docteur es, Biologie Santé, 2018, Montpellier

L’un des objectifs principal de la biologie synthétique est de reprogrammer les organismes vivants pour résoudre des challenges mondiaux actuelles dans le domaine industriel, environnemental… (more)

Subjects/Keywords: Biologie synthétique; Biocomputing; Recombinase; Synthetic biology; Biocomputing; Recombinase

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APA (6th Edition):

Guiziou, S. (2018). Engineering framework for scalable recombinase logic operating in living cells : Développement d'un cadre systématique pour l'implémentation de logique dans les organismes vivants en utilisant les recombinases. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2018MONTT026

Chicago Manual of Style (16th Edition):

Guiziou, Sarah. “Engineering framework for scalable recombinase logic operating in living cells : Développement d'un cadre systématique pour l'implémentation de logique dans les organismes vivants en utilisant les recombinases.” 2018. Doctoral Dissertation, Montpellier. Accessed May 25, 2019. http://www.theses.fr/2018MONTT026.

MLA Handbook (7th Edition):

Guiziou, Sarah. “Engineering framework for scalable recombinase logic operating in living cells : Développement d'un cadre systématique pour l'implémentation de logique dans les organismes vivants en utilisant les recombinases.” 2018. Web. 25 May 2019.

Vancouver:

Guiziou S. Engineering framework for scalable recombinase logic operating in living cells : Développement d'un cadre systématique pour l'implémentation de logique dans les organismes vivants en utilisant les recombinases. [Internet] [Doctoral dissertation]. Montpellier; 2018. [cited 2019 May 25]. Available from: http://www.theses.fr/2018MONTT026.

Council of Science Editors:

Guiziou S. Engineering framework for scalable recombinase logic operating in living cells : Développement d'un cadre systématique pour l'implémentation de logique dans les organismes vivants en utilisant les recombinases. [Doctoral Dissertation]. Montpellier; 2018. Available from: http://www.theses.fr/2018MONTT026


University of California – Berkeley

3. Hsiau, Timothy. Tools for engineering biology: methods for designing, building, and testing.

Degree: Bioengineering, 2013, University of California – Berkeley

 Genetic engineering remains a difficult task and the design, build, test cycle may take months or years to complete. Currently, all three aspects are laborious,… (more)

Subjects/Keywords: Molecular biology; synthetic biology

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APA (6th Edition):

Hsiau, T. (2013). Tools for engineering biology: methods for designing, building, and testing. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1w32c0hq

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):

Hsiau, Timothy. “Tools for engineering biology: methods for designing, building, and testing.” 2013. Thesis, University of California – Berkeley. Accessed May 25, 2019. http://www.escholarship.org/uc/item/1w32c0hq.

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

MLA Handbook (7th Edition):

Hsiau, Timothy. “Tools for engineering biology: methods for designing, building, and testing.” 2013. Web. 25 May 2019.

Vancouver:

Hsiau T. Tools for engineering biology: methods for designing, building, and testing. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 May 25]. Available from: http://www.escholarship.org/uc/item/1w32c0hq.

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

Council of Science Editors:

Hsiau T. Tools for engineering biology: methods for designing, building, and testing. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/1w32c0hq

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


University of Ottawa

4. Salem, Danny. Using the Tandem Fluorescent Timer as a Reporter of Dynamic Gene Regulation .

Degree: 2019, University of Ottawa

 I propose the use of the tandem fluorescent timer protein as a reporter of dynamic gene regulation. The tandem fluorescent timer is a fusion of… (more)

Subjects/Keywords: Synthetic Biology; Systems Biology; Bioinformatics

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APA (6th Edition):

Salem, D. (2019). Using the Tandem Fluorescent Timer as a Reporter of Dynamic Gene Regulation . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/39021

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):

Salem, Danny. “Using the Tandem Fluorescent Timer as a Reporter of Dynamic Gene Regulation .” 2019. Thesis, University of Ottawa. Accessed May 25, 2019. http://hdl.handle.net/10393/39021.

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

MLA Handbook (7th Edition):

Salem, Danny. “Using the Tandem Fluorescent Timer as a Reporter of Dynamic Gene Regulation .” 2019. Web. 25 May 2019.

Vancouver:

Salem D. Using the Tandem Fluorescent Timer as a Reporter of Dynamic Gene Regulation . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2019 May 25]. Available from: http://hdl.handle.net/10393/39021.

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

Council of Science Editors:

Salem D. Using the Tandem Fluorescent Timer as a Reporter of Dynamic Gene Regulation . [Thesis]. University of Ottawa; 2019. Available from: http://hdl.handle.net/10393/39021

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


ETH Zürich

5. Dietz, Sven Lucas. Characterization of genetic functional elements physically coupled to NGS sequencing.

Degree: 2016, ETH Zürich

 The construction of complex systems in living organisms depends on standardized parts. This main paradigm rests on long established standards in other, very successful, engineering… (more)

Subjects/Keywords: Biology; Synthetic Biology; NGS; Screening

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APA (6th Edition):

Dietz, S. L. (2016). Characterization of genetic functional elements physically coupled to NGS sequencing. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/116

Chicago Manual of Style (16th Edition):

Dietz, Sven Lucas. “Characterization of genetic functional elements physically coupled to NGS sequencing.” 2016. Doctoral Dissertation, ETH Zürich. Accessed May 25, 2019. http://hdl.handle.net/20.500.11850/116.

MLA Handbook (7th Edition):

Dietz, Sven Lucas. “Characterization of genetic functional elements physically coupled to NGS sequencing.” 2016. Web. 25 May 2019.

Vancouver:

Dietz SL. Characterization of genetic functional elements physically coupled to NGS sequencing. [Internet] [Doctoral dissertation]. ETH Zürich; 2016. [cited 2019 May 25]. Available from: http://hdl.handle.net/20.500.11850/116.

Council of Science Editors:

Dietz SL. Characterization of genetic functional elements physically coupled to NGS sequencing. [Doctoral Dissertation]. ETH Zürich; 2016. Available from: http://hdl.handle.net/20.500.11850/116


University of Washington

6. Pierre-Jerome, Edith. Tuning the auxin transcriptional response.

Degree: PhD, 2016, University of Washington

 Auxin is involved in almost every aspect of plant growth and development. How auxin orchestrates such diverse and context-specific responses has been a longstanding question.… (more)

Subjects/Keywords: auxin; synthetic biology; transcription; Molecular biology; biology

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APA (6th Edition):

Pierre-Jerome, E. (2016). Tuning the auxin transcriptional response. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/35135

Chicago Manual of Style (16th Edition):

Pierre-Jerome, Edith. “Tuning the auxin transcriptional response.” 2016. Doctoral Dissertation, University of Washington. Accessed May 25, 2019. http://hdl.handle.net/1773/35135.

MLA Handbook (7th Edition):

Pierre-Jerome, Edith. “Tuning the auxin transcriptional response.” 2016. Web. 25 May 2019.

Vancouver:

Pierre-Jerome E. Tuning the auxin transcriptional response. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2019 May 25]. Available from: http://hdl.handle.net/1773/35135.

Council of Science Editors:

Pierre-Jerome E. Tuning the auxin transcriptional response. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/35135


University of California – San Diego

7. Miyake-Stoner, Shigeki Joseph. Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms.

Degree: Biology, 2016, University of California – San Diego

 A promising new strategy for cancer therapy is the use of engineered oncolytic viruses, adapted from their natural properties of seeking out and destroying cells… (more)

Subjects/Keywords: Biology; Adenovirus; Cancer; Oncolytic; Synthetic

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APA (6th Edition):

Miyake-Stoner, S. J. (2016). Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/7qg226zn

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):

Miyake-Stoner, Shigeki Joseph. “Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms.” 2016. Thesis, University of California – San Diego. Accessed May 25, 2019. http://www.escholarship.org/uc/item/7qg226zn.

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

MLA Handbook (7th Edition):

Miyake-Stoner, Shigeki Joseph. “Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms.” 2016. Web. 25 May 2019.

Vancouver:

Miyake-Stoner SJ. Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2019 May 25]. Available from: http://www.escholarship.org/uc/item/7qg226zn.

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

Council of Science Editors:

Miyake-Stoner SJ. Engineering tumor-specific oncolytic adenoviruses with small molecule-controlled expanded tropisms. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/7qg226zn

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


University of California – Berkeley

8. Huh, Jin Hang. Protein Delivery to Eukaryotic Cells by Engineered Bacteria.

Degree: Bioengineering, 2012, University of California – Berkeley

Synthetic biologists engineer genetic circuits for applications ranging from biosynthesis to biotherapeutics. Although the application of engineering strategies such as standardization, abstraction, and modularity has… (more)

Subjects/Keywords: Biomedical engineering; Synthetic biology

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APA (6th Edition):

Huh, J. H. (2012). Protein Delivery to Eukaryotic Cells by Engineered Bacteria. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/519059r3

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):

Huh, Jin Hang. “Protein Delivery to Eukaryotic Cells by Engineered Bacteria.” 2012. Thesis, University of California – Berkeley. Accessed May 25, 2019. http://www.escholarship.org/uc/item/519059r3.

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

MLA Handbook (7th Edition):

Huh, Jin Hang. “Protein Delivery to Eukaryotic Cells by Engineered Bacteria.” 2012. Web. 25 May 2019.

Vancouver:

Huh JH. Protein Delivery to Eukaryotic Cells by Engineered Bacteria. [Internet] [Thesis]. University of California – Berkeley; 2012. [cited 2019 May 25]. Available from: http://www.escholarship.org/uc/item/519059r3.

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

Council of Science Editors:

Huh JH. Protein Delivery to Eukaryotic Cells by Engineered Bacteria. [Thesis]. University of California – Berkeley; 2012. Available from: http://www.escholarship.org/uc/item/519059r3

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


Virginia Tech

9. Hochendoner, Philip Louis. Entrainment of Bacterial Synthetic Oscillators using Proteolytic Queueing and Aperiodic Signaling.

Degree: PhD, Physics, 2015, Virginia Tech

 The bulk of this thesis considers how biological rhythms (oscillators) can be made to synchronize their rhythms by virtue of coupling to an external signal.… (more)

Subjects/Keywords: Biophysics; Synthetic Biology; Entrainment; Queueing

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APA (6th Edition):

Hochendoner, P. L. (2015). Entrainment of Bacterial Synthetic Oscillators using Proteolytic Queueing and Aperiodic Signaling. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/64373

Chicago Manual of Style (16th Edition):

Hochendoner, Philip Louis. “Entrainment of Bacterial Synthetic Oscillators using Proteolytic Queueing and Aperiodic Signaling.” 2015. Doctoral Dissertation, Virginia Tech. Accessed May 25, 2019. http://hdl.handle.net/10919/64373.

MLA Handbook (7th Edition):

Hochendoner, Philip Louis. “Entrainment of Bacterial Synthetic Oscillators using Proteolytic Queueing and Aperiodic Signaling.” 2015. Web. 25 May 2019.

Vancouver:

Hochendoner PL. Entrainment of Bacterial Synthetic Oscillators using Proteolytic Queueing and Aperiodic Signaling. [Internet] [Doctoral dissertation]. Virginia Tech; 2015. [cited 2019 May 25]. Available from: http://hdl.handle.net/10919/64373.

Council of Science Editors:

Hochendoner PL. Entrainment of Bacterial Synthetic Oscillators using Proteolytic Queueing and Aperiodic Signaling. [Doctoral Dissertation]. Virginia Tech; 2015. Available from: http://hdl.handle.net/10919/64373


Cornell University

10. Takahashi, Melissa. Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks .

Degree: 2015, Cornell University

 A major goal of synthetic biology is to reliably engineer microorganisms to perform a variety of functions with impact in the fields of biotechnology and… (more)

Subjects/Keywords: RNA synthetic biology; transcription regulation

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APA (6th Edition):

Takahashi, M. (2015). Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/41135

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):

Takahashi, Melissa. “Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks .” 2015. Thesis, Cornell University. Accessed May 25, 2019. http://hdl.handle.net/1813/41135.

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

MLA Handbook (7th Edition):

Takahashi, Melissa. “Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks .” 2015. Web. 25 May 2019.

Vancouver:

Takahashi M. Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 May 25]. Available from: http://hdl.handle.net/1813/41135.

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

Council of Science Editors:

Takahashi M. Developing Design Principles For Engineering Rna Transcription Regulators And Rna Synthetic Gene Networks . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41135

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


University of Ottawa

11. Roney, Ian James. Construction and Optimization of Tetracycline-Responsive Gene Expression Systems .

Degree: 2016, University of Ottawa

 Conditional gene expression systems that enable inducible and reversible transcriptional control are essential research tools and have broad applications in biomedicine and biotechnology. The reverse… (more)

Subjects/Keywords: Synthetic Biology; Gene Expression Systems

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APA (6th Edition):

Roney, I. J. (2016). Construction and Optimization of Tetracycline-Responsive Gene Expression Systems . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35058

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):

Roney, Ian James. “Construction and Optimization of Tetracycline-Responsive Gene Expression Systems .” 2016. Thesis, University of Ottawa. Accessed May 25, 2019. http://hdl.handle.net/10393/35058.

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

MLA Handbook (7th Edition):

Roney, Ian James. “Construction and Optimization of Tetracycline-Responsive Gene Expression Systems .” 2016. Web. 25 May 2019.

Vancouver:

Roney IJ. Construction and Optimization of Tetracycline-Responsive Gene Expression Systems . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2019 May 25]. Available from: http://hdl.handle.net/10393/35058.

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

Council of Science Editors:

Roney IJ. Construction and Optimization of Tetracycline-Responsive Gene Expression Systems . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35058

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


University of Toronto

12. Nagaraj, Seema. Transcriptional Regulation in Synthetic Gene Networks.

Degree: 2010, University of Toronto

The study of synthetic gene regulatory networks allows the isolation and investigation of components and motifs in natural regulatory networks. Many synthetic gene networks are… (more)

Subjects/Keywords: synthetic biology; genetic circuits; 0541

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APA (6th Edition):

Nagaraj, S. (2010). Transcriptional Regulation in Synthetic Gene Networks. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/24838

Chicago Manual of Style (16th Edition):

Nagaraj, Seema. “Transcriptional Regulation in Synthetic Gene Networks.” 2010. Doctoral Dissertation, University of Toronto. Accessed May 25, 2019. http://hdl.handle.net/1807/24838.

MLA Handbook (7th Edition):

Nagaraj, Seema. “Transcriptional Regulation in Synthetic Gene Networks.” 2010. Web. 25 May 2019.

Vancouver:

Nagaraj S. Transcriptional Regulation in Synthetic Gene Networks. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2019 May 25]. Available from: http://hdl.handle.net/1807/24838.

Council of Science Editors:

Nagaraj S. Transcriptional Regulation in Synthetic Gene Networks. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24838


Columbia University

13. Ostrov, Nili. Expanding Biological Engineering from Single Enzymes to Cellular Pathways.

Degree: 2012, Columbia University

 The emerging field of synthetic biology evolved from biological research much the same way synthetic chemistry evolved from chemical research; with accumulated knowledge of the… (more)

Subjects/Keywords: Synthetic biology; Genetics; Microbiology

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APA (6th Edition):

Ostrov, N. (2012). Expanding Biological Engineering from Single Enzymes to Cellular Pathways. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8M043GN

Chicago Manual of Style (16th Edition):

Ostrov, Nili. “Expanding Biological Engineering from Single Enzymes to Cellular Pathways.” 2012. Doctoral Dissertation, Columbia University. Accessed May 25, 2019. https://doi.org/10.7916/D8M043GN.

MLA Handbook (7th Edition):

Ostrov, Nili. “Expanding Biological Engineering from Single Enzymes to Cellular Pathways.” 2012. Web. 25 May 2019.

Vancouver:

Ostrov N. Expanding Biological Engineering from Single Enzymes to Cellular Pathways. [Internet] [Doctoral dissertation]. Columbia University; 2012. [cited 2019 May 25]. Available from: https://doi.org/10.7916/D8M043GN.

Council of Science Editors:

Ostrov N. Expanding Biological Engineering from Single Enzymes to Cellular Pathways. [Doctoral Dissertation]. Columbia University; 2012. Available from: https://doi.org/10.7916/D8M043GN


University of Oxford

14. Spratt, Joel. DNA-templated assembly of the bacterial flagellar motor's cytoplasmic ring.

Degree: PhD, 2018, University of Oxford

 The bacterial flagellar motor is one of the most complex protein machines found in nature and how it self-assembles and produces force are very much… (more)

Subjects/Keywords: Synthetic Biology; Biophysics; Protein Biochemistry

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APA (6th Edition):

Spratt, J. (2018). DNA-templated assembly of the bacterial flagellar motor's cytoplasmic ring. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:27428b51-4fb8-4964-95b6-d3cbb5db996d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770682

Chicago Manual of Style (16th Edition):

Spratt, Joel. “DNA-templated assembly of the bacterial flagellar motor's cytoplasmic ring.” 2018. Doctoral Dissertation, University of Oxford. Accessed May 25, 2019. http://ora.ox.ac.uk/objects/uuid:27428b51-4fb8-4964-95b6-d3cbb5db996d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770682.

MLA Handbook (7th Edition):

Spratt, Joel. “DNA-templated assembly of the bacterial flagellar motor's cytoplasmic ring.” 2018. Web. 25 May 2019.

Vancouver:

Spratt J. DNA-templated assembly of the bacterial flagellar motor's cytoplasmic ring. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2019 May 25]. Available from: http://ora.ox.ac.uk/objects/uuid:27428b51-4fb8-4964-95b6-d3cbb5db996d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770682.

Council of Science Editors:

Spratt J. DNA-templated assembly of the bacterial flagellar motor's cytoplasmic ring. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:27428b51-4fb8-4964-95b6-d3cbb5db996d ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770682

15. Rideau, Fabien. Clonage et modification du génome de Mycoplasma hominis dans la levure Saccharomyces cerevisiae : Development of genetic tools for Mycoplasma hominis with synthetic biology approach.

Degree: Docteur es, Microbiologie-immunologie, 2018, Bordeaux

 Mycoplasma hominis est un pathogène humain opportuniste responsable d’infections génitales et néo-natales. Modifier génétiquement cette bactérie est nécessaire afin de comprendre les mécanismes de virulence… (more)

Subjects/Keywords: Mycoplasma hominis; Biologie de synthèse; CRISPR; Cas9; Transformation; Mycoplasma hominis; Synthetic Biology; CRISPR; Cas9; Transformation

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APA (6th Edition):

Rideau, F. (2018). Clonage et modification du génome de Mycoplasma hominis dans la levure Saccharomyces cerevisiae : Development of genetic tools for Mycoplasma hominis with synthetic biology approach. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2018BORD0227

Chicago Manual of Style (16th Edition):

Rideau, Fabien. “Clonage et modification du génome de Mycoplasma hominis dans la levure Saccharomyces cerevisiae : Development of genetic tools for Mycoplasma hominis with synthetic biology approach.” 2018. Doctoral Dissertation, Bordeaux. Accessed May 25, 2019. http://www.theses.fr/2018BORD0227.

MLA Handbook (7th Edition):

Rideau, Fabien. “Clonage et modification du génome de Mycoplasma hominis dans la levure Saccharomyces cerevisiae : Development of genetic tools for Mycoplasma hominis with synthetic biology approach.” 2018. Web. 25 May 2019.

Vancouver:

Rideau F. Clonage et modification du génome de Mycoplasma hominis dans la levure Saccharomyces cerevisiae : Development of genetic tools for Mycoplasma hominis with synthetic biology approach. [Internet] [Doctoral dissertation]. Bordeaux; 2018. [cited 2019 May 25]. Available from: http://www.theses.fr/2018BORD0227.

Council of Science Editors:

Rideau F. Clonage et modification du génome de Mycoplasma hominis dans la levure Saccharomyces cerevisiae : Development of genetic tools for Mycoplasma hominis with synthetic biology approach. [Doctoral Dissertation]. Bordeaux; 2018. Available from: http://www.theses.fr/2018BORD0227


University of California – Berkeley

16. Davis, Matthew Aaron. Exploring in vivo biochemistry with C4 fuel and commodity chemical pathways.

Degree: Molecular & Cell Biology, 2015, University of California – Berkeley

 The biological diversity found throughout the world contains equally wondrous chemical diversity that can operate with the precision, efficiency, and scale that humanity has yet… (more)

Subjects/Keywords: Biochemistry; Molecular biology; metabolic engineering; synthetic biology

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APA (6th Edition):

Davis, M. A. (2015). Exploring in vivo biochemistry with C4 fuel and commodity chemical pathways. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4q39633k

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):

Davis, Matthew Aaron. “Exploring in vivo biochemistry with C4 fuel and commodity chemical pathways.” 2015. Thesis, University of California – Berkeley. Accessed May 25, 2019. http://www.escholarship.org/uc/item/4q39633k.

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

MLA Handbook (7th Edition):

Davis, Matthew Aaron. “Exploring in vivo biochemistry with C4 fuel and commodity chemical pathways.” 2015. Web. 25 May 2019.

Vancouver:

Davis MA. Exploring in vivo biochemistry with C4 fuel and commodity chemical pathways. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 May 25]. Available from: http://www.escholarship.org/uc/item/4q39633k.

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

Council of Science Editors:

Davis MA. Exploring in vivo biochemistry with C4 fuel and commodity chemical pathways. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/4q39633k

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


Boston University

17. Banerjee, Swati. Reliable gene expression and assembly for synthetic biological devices in E. coli through customized promoter insulator elements and automated DNA assembly.

Degree: PhD, Molecular Biology, Cell Biology & Biochemistry, 2016, Boston University

 Building reliable genetic devices in synthetic biology is still a major challenge despite the various advances that have been made in the field since its… (more)

Subjects/Keywords: Molecular biology; Bioengineering; Genetic engineering; Synthetic biology

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APA (6th Edition):

Banerjee, S. (2016). Reliable gene expression and assembly for synthetic biological devices in E. coli through customized promoter insulator elements and automated DNA assembly. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/19718

Chicago Manual of Style (16th Edition):

Banerjee, Swati. “Reliable gene expression and assembly for synthetic biological devices in E. coli through customized promoter insulator elements and automated DNA assembly.” 2016. Doctoral Dissertation, Boston University. Accessed May 25, 2019. http://hdl.handle.net/2144/19718.

MLA Handbook (7th Edition):

Banerjee, Swati. “Reliable gene expression and assembly for synthetic biological devices in E. coli through customized promoter insulator elements and automated DNA assembly.” 2016. Web. 25 May 2019.

Vancouver:

Banerjee S. Reliable gene expression and assembly for synthetic biological devices in E. coli through customized promoter insulator elements and automated DNA assembly. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2019 May 25]. Available from: http://hdl.handle.net/2144/19718.

Council of Science Editors:

Banerjee S. Reliable gene expression and assembly for synthetic biological devices in E. coli through customized promoter insulator elements and automated DNA assembly. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/19718


University of Toronto

18. Bagh, Sangram. Systems and Synthetic Biology in E. coli Cells Quantitative System Characterization, Programming and Engineering Novel Cellular Functions.

Degree: 2010, University of Toronto

The emerging field of synthetic biology aims to use artificially designed genetic circuits to program living cells, much as engineers program a computer or control… (more)

Subjects/Keywords: Synthetic Biology, Systems Biology; Physical Chemistry

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APA (6th Edition):

Bagh, S. (2010). Systems and Synthetic Biology in E. coli Cells Quantitative System Characterization, Programming and Engineering Novel Cellular Functions. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/26128

Chicago Manual of Style (16th Edition):

Bagh, Sangram. “Systems and Synthetic Biology in E. coli Cells Quantitative System Characterization, Programming and Engineering Novel Cellular Functions.” 2010. Doctoral Dissertation, University of Toronto. Accessed May 25, 2019. http://hdl.handle.net/1807/26128.

MLA Handbook (7th Edition):

Bagh, Sangram. “Systems and Synthetic Biology in E. coli Cells Quantitative System Characterization, Programming and Engineering Novel Cellular Functions.” 2010. Web. 25 May 2019.

Vancouver:

Bagh S. Systems and Synthetic Biology in E. coli Cells Quantitative System Characterization, Programming and Engineering Novel Cellular Functions. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2019 May 25]. Available from: http://hdl.handle.net/1807/26128.

Council of Science Editors:

Bagh S. Systems and Synthetic Biology in E. coli Cells Quantitative System Characterization, Programming and Engineering Novel Cellular Functions. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/26128


University of California – San Francisco

19. Williams, Reid Edward. Rewiring Eukaryotic Signaling Networks using Synthetic Posttranslational Connections.

Degree: Biophysics, 2013, University of California – San Francisco

 Cells are dynamic, adaptive structures – able to sense their environment and change their behavior accordingly. This ability is largely driven by signaling pathways – networks of… (more)

Subjects/Keywords: Biophysics; Cellular biology; kinases; signaling; synthetic biology

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APA (6th Edition):

Williams, R. E. (2013). Rewiring Eukaryotic Signaling Networks using Synthetic Posttranslational Connections. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/56w4794w

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, Reid Edward. “Rewiring Eukaryotic Signaling Networks using Synthetic Posttranslational Connections.” 2013. Thesis, University of California – San Francisco. Accessed May 25, 2019. http://www.escholarship.org/uc/item/56w4794w.

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

MLA Handbook (7th Edition):

Williams, Reid Edward. “Rewiring Eukaryotic Signaling Networks using Synthetic Posttranslational Connections.” 2013. Web. 25 May 2019.

Vancouver:

Williams RE. Rewiring Eukaryotic Signaling Networks using Synthetic Posttranslational Connections. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2019 May 25]. Available from: http://www.escholarship.org/uc/item/56w4794w.

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

Council of Science Editors:

Williams RE. Rewiring Eukaryotic Signaling Networks using Synthetic Posttranslational Connections. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/56w4794w

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


University of Oxford

20. Michaels, Yale. Fine tuning gene expression levels in mammalian cells with engineered microRNA target sites.

Degree: PhD, 2018, University of Oxford

 Precise, analogue regulation of gene expression is critical for development, homeostasis and regeneration in mammals. In contrast, widely employed experimental and therapeutic approaches such as… (more)

Subjects/Keywords: Synthetic biology; Genome Engineering; Molecular biology

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APA (6th Edition):

Michaels, Y. (2018). Fine tuning gene expression levels in mammalian cells with engineered microRNA target sites. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:204ab084-9a54-4e14-8a75-bd7042584de5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770678

Chicago Manual of Style (16th Edition):

Michaels, Yale. “Fine tuning gene expression levels in mammalian cells with engineered microRNA target sites.” 2018. Doctoral Dissertation, University of Oxford. Accessed May 25, 2019. http://ora.ox.ac.uk/objects/uuid:204ab084-9a54-4e14-8a75-bd7042584de5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770678.

MLA Handbook (7th Edition):

Michaels, Yale. “Fine tuning gene expression levels in mammalian cells with engineered microRNA target sites.” 2018. Web. 25 May 2019.

Vancouver:

Michaels Y. Fine tuning gene expression levels in mammalian cells with engineered microRNA target sites. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2019 May 25]. Available from: http://ora.ox.ac.uk/objects/uuid:204ab084-9a54-4e14-8a75-bd7042584de5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770678.

Council of Science Editors:

Michaels Y. Fine tuning gene expression levels in mammalian cells with engineered microRNA target sites. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:204ab084-9a54-4e14-8a75-bd7042584de5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.770678


George Mason University

21. Fye-Marnien, Shannon. An Examination of Contingency in Synthetic Genomics Research and Implications for National Security .

Degree: 2015, George Mason University

 The fields of synthetic genomics and synthetic biology have garnered much attention in the biodefense community and the general public due to their dual-use nature:… (more)

Subjects/Keywords: International relations; gene synthesis; synthetic biology; synthetic genomics; terrorism

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APA (6th Edition):

Fye-Marnien, S. (2015). An Examination of Contingency in Synthetic Genomics Research and Implications for National Security . (Thesis). George Mason University. Retrieved from http://hdl.handle.net/1920/10188

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):

Fye-Marnien, Shannon. “An Examination of Contingency in Synthetic Genomics Research and Implications for National Security .” 2015. Thesis, George Mason University. Accessed May 25, 2019. http://hdl.handle.net/1920/10188.

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

MLA Handbook (7th Edition):

Fye-Marnien, Shannon. “An Examination of Contingency in Synthetic Genomics Research and Implications for National Security .” 2015. Web. 25 May 2019.

Vancouver:

Fye-Marnien S. An Examination of Contingency in Synthetic Genomics Research and Implications for National Security . [Internet] [Thesis]. George Mason University; 2015. [cited 2019 May 25]. Available from: http://hdl.handle.net/1920/10188.

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

Council of Science Editors:

Fye-Marnien S. An Examination of Contingency in Synthetic Genomics Research and Implications for National Security . [Thesis]. George Mason University; 2015. Available from: http://hdl.handle.net/1920/10188

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

22. Yandrapalli, Naresh. Role of HIV-1 Gag protein multimerization in the generation of nanodomains in lipid membranes : Rôle de la multimérisation de la protéine Gag du HIV-1 dans la génération de nanodomaines lipidiques membranaires.

Degree: Docteur es, Biologie Santé, 2016, Montpellier

 La polyprotéine Gag du VIH-1 qui contient quatre principaux domaines (Matrix (MA), capside (CA), nucléocapside (NC), et P6) est l’orchestrateur privilégié de l'assemblage du virus… (more)

Subjects/Keywords: Domaines membranaires; Virologie; Biophotonique; Hiv; Auto-Assemblage; Biologie synthétique; Membrane domains; Virology; Biophotonics; Hiv; Self-Assembly; Synthetic biology

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APA (6th Edition):

Yandrapalli, N. (2016). Role of HIV-1 Gag protein multimerization in the generation of nanodomains in lipid membranes : Rôle de la multimérisation de la protéine Gag du HIV-1 dans la génération de nanodomaines lipidiques membranaires. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2016MONTT097

Chicago Manual of Style (16th Edition):

Yandrapalli, Naresh. “Role of HIV-1 Gag protein multimerization in the generation of nanodomains in lipid membranes : Rôle de la multimérisation de la protéine Gag du HIV-1 dans la génération de nanodomaines lipidiques membranaires.” 2016. Doctoral Dissertation, Montpellier. Accessed May 25, 2019. http://www.theses.fr/2016MONTT097.

MLA Handbook (7th Edition):

Yandrapalli, Naresh. “Role of HIV-1 Gag protein multimerization in the generation of nanodomains in lipid membranes : Rôle de la multimérisation de la protéine Gag du HIV-1 dans la génération de nanodomaines lipidiques membranaires.” 2016. Web. 25 May 2019.

Vancouver:

Yandrapalli N. Role of HIV-1 Gag protein multimerization in the generation of nanodomains in lipid membranes : Rôle de la multimérisation de la protéine Gag du HIV-1 dans la génération de nanodomaines lipidiques membranaires. [Internet] [Doctoral dissertation]. Montpellier; 2016. [cited 2019 May 25]. Available from: http://www.theses.fr/2016MONTT097.

Council of Science Editors:

Yandrapalli N. Role of HIV-1 Gag protein multimerization in the generation of nanodomains in lipid membranes : Rôle de la multimérisation de la protéine Gag du HIV-1 dans la génération de nanodomaines lipidiques membranaires. [Doctoral Dissertation]. Montpellier; 2016. Available from: http://www.theses.fr/2016MONTT097

23. Libis, Vincent. New inputs for synthetic biological systems : Nouvelles stratégies d’induction pour systèmes biologiques synthétiques.

Degree: Docteur es, Frontières du vivant, 2016, Sorbonne Paris Cité

Les chercheurs en biologie de synthèse programment l’ADN pour construire des systèmes biologiques capables de répondre à certaines conditions de manière prédéfinie. Cette capacité pourrait… (more)

Subjects/Keywords: Biosenseur; Ingénierie métabolique; Biologie de synthèse; Facteur de transcription; Induction; Phages; Biosensor; Metabolic engineering; Synthetic biology; Transcription factor; Induction; Phages

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APA (6th Edition):

Libis, V. (2016). New inputs for synthetic biological systems : Nouvelles stratégies d’induction pour systèmes biologiques synthétiques. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCC127

Chicago Manual of Style (16th Edition):

Libis, Vincent. “New inputs for synthetic biological systems : Nouvelles stratégies d’induction pour systèmes biologiques synthétiques.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed May 25, 2019. http://www.theses.fr/2016USPCC127.

MLA Handbook (7th Edition):

Libis, Vincent. “New inputs for synthetic biological systems : Nouvelles stratégies d’induction pour systèmes biologiques synthétiques.” 2016. Web. 25 May 2019.

Vancouver:

Libis V. New inputs for synthetic biological systems : Nouvelles stratégies d’induction pour systèmes biologiques synthétiques. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 May 25]. Available from: http://www.theses.fr/2016USPCC127.

Council of Science Editors:

Libis V. New inputs for synthetic biological systems : Nouvelles stratégies d’induction pour systèmes biologiques synthétiques. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCC127


Université de Grenoble

24. Baptist, Guillaume. Réseaux de régulation chez Escherichia coli : Gene regulatory network in Escherichia coli.

Degree: Docteur es, Virologie Microbiologie Immunologie, 2012, Université de Grenoble

L'adaptation d'une bactérie aux changements de son environnement est contrôlée par un réseau de régulation large et complexe, faisant intervenir de nombreux acteurs et modules… (more)

Subjects/Keywords: Réseaux de régulation; Biologie synthétique; Gènes rapporteurs; Répression catabolique; Regulatory network; Synthetic biology; Reporter genes; Catabolite repression

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APA (6th Edition):

Baptist, G. (2012). Réseaux de régulation chez Escherichia coli : Gene regulatory network in Escherichia coli. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2012GRENV040

Chicago Manual of Style (16th Edition):

Baptist, Guillaume. “Réseaux de régulation chez Escherichia coli : Gene regulatory network in Escherichia coli.” 2012. Doctoral Dissertation, Université de Grenoble. Accessed May 25, 2019. http://www.theses.fr/2012GRENV040.

MLA Handbook (7th Edition):

Baptist, Guillaume. “Réseaux de régulation chez Escherichia coli : Gene regulatory network in Escherichia coli.” 2012. Web. 25 May 2019.

Vancouver:

Baptist G. Réseaux de régulation chez Escherichia coli : Gene regulatory network in Escherichia coli. [Internet] [Doctoral dissertation]. Université de Grenoble; 2012. [cited 2019 May 25]. Available from: http://www.theses.fr/2012GRENV040.

Council of Science Editors:

Baptist G. Réseaux de régulation chez Escherichia coli : Gene regulatory network in Escherichia coli. [Doctoral Dissertation]. Université de Grenoble; 2012. Available from: http://www.theses.fr/2012GRENV040


Université de Grenoble

25. Izard, Jerome. Contrôle de la croissance et régulation génique chez Escherichia coli : Growth control and gene regulation in Escherichia coli.

Degree: Docteur es, Médecine, 2012, Université de Grenoble

La faculté d’adaptation aux conditions environnementales des bactéries provient de lacomplexité de leur réseau de régulation génique, impliquant de nombreux régulateursspécifiques et la machinerie d’expression… (more)

Subjects/Keywords: Croissance; Régulation; Expression génique; ARN polymerase; Crl; Biologie synthétique; Growth; Regulation; Gene expression; RNA polymerase; Crl; Synthetic biology

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APA (6th Edition):

Izard, J. (2012). Contrôle de la croissance et régulation génique chez Escherichia coli : Growth control and gene regulation in Escherichia coli. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2012GRENV061

Chicago Manual of Style (16th Edition):

Izard, Jerome. “Contrôle de la croissance et régulation génique chez Escherichia coli : Growth control and gene regulation in Escherichia coli.” 2012. Doctoral Dissertation, Université de Grenoble. Accessed May 25, 2019. http://www.theses.fr/2012GRENV061.

MLA Handbook (7th Edition):

Izard, Jerome. “Contrôle de la croissance et régulation génique chez Escherichia coli : Growth control and gene regulation in Escherichia coli.” 2012. Web. 25 May 2019.

Vancouver:

Izard J. Contrôle de la croissance et régulation génique chez Escherichia coli : Growth control and gene regulation in Escherichia coli. [Internet] [Doctoral dissertation]. Université de Grenoble; 2012. [cited 2019 May 25]. Available from: http://www.theses.fr/2012GRENV061.

Council of Science Editors:

Izard J. Contrôle de la croissance et régulation génique chez Escherichia coli : Growth control and gene regulation in Escherichia coli. [Doctoral Dissertation]. Université de Grenoble; 2012. Available from: http://www.theses.fr/2012GRENV061

26. Pinhal, Stéphane. Mécanismes de l'inhibition de la croissance par l'acétate chez Escherichia coli : Mechanisms of the inhibition of the growth of Escherichia coli by the acetate.

Degree: Docteur es, Virologie microbiologie immunologie, 2015, Grenoble Alpes

L'acétate nuit à la croissance de la bactérie E. coli. Malgré les recherches qui tentent d'en d'écrire les raisons, il nous est impossible actuellement de… (more)

Subjects/Keywords: Inhibition; Croissance; Acétate; Métabolisme; Escherichia coli; Biologie synthétique; IGEM; Inhibition; Growth; Acetate; Metabolism; Escherichia coli; Synthetic biology; IGEM; 570

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APA (6th Edition):

Pinhal, S. (2015). Mécanismes de l'inhibition de la croissance par l'acétate chez Escherichia coli : Mechanisms of the inhibition of the growth of Escherichia coli by the acetate. (Doctoral Dissertation). Grenoble Alpes. Retrieved from http://www.theses.fr/2015GREAV003

Chicago Manual of Style (16th Edition):

Pinhal, Stéphane. “Mécanismes de l'inhibition de la croissance par l'acétate chez Escherichia coli : Mechanisms of the inhibition of the growth of Escherichia coli by the acetate.” 2015. Doctoral Dissertation, Grenoble Alpes. Accessed May 25, 2019. http://www.theses.fr/2015GREAV003.

MLA Handbook (7th Edition):

Pinhal, Stéphane. “Mécanismes de l'inhibition de la croissance par l'acétate chez Escherichia coli : Mechanisms of the inhibition of the growth of Escherichia coli by the acetate.” 2015. Web. 25 May 2019.

Vancouver:

Pinhal S. Mécanismes de l'inhibition de la croissance par l'acétate chez Escherichia coli : Mechanisms of the inhibition of the growth of Escherichia coli by the acetate. [Internet] [Doctoral dissertation]. Grenoble Alpes; 2015. [cited 2019 May 25]. Available from: http://www.theses.fr/2015GREAV003.

Council of Science Editors:

Pinhal S. Mécanismes de l'inhibition de la croissance par l'acétate chez Escherichia coli : Mechanisms of the inhibition of the growth of Escherichia coli by the acetate. [Doctoral Dissertation]. Grenoble Alpes; 2015. Available from: http://www.theses.fr/2015GREAV003


Université Montpellier II

27. Rialle, Stéphanie. Méthodologie et outils bioinformatiques d'aide à la conception de systèmes biologiques synthétiques pour de nouveaux diagnostics en santé humaine : Methodology and bioinformatics tools to design synthetic biological systems for new human health diagnosis.

Degree: Docteur es, Informatique, 2010, Université Montpellier II

La biologie synthétique est une discipline en pleine expansion visant à concevoir et construire des systèmes biologiques possédant des fonctions qui n'existent pas dans la… (more)

Subjects/Keywords: Biologie synthétique; Bioinformatique; Conception; Modélisation; Base de données; Logiciel; Synthetic biology; Bioinformatics; Design; Modelling; Database; Software

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APA (6th Edition):

Rialle, S. (2010). Méthodologie et outils bioinformatiques d'aide à la conception de systèmes biologiques synthétiques pour de nouveaux diagnostics en santé humaine : Methodology and bioinformatics tools to design synthetic biological systems for new human health diagnosis. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2010MON20091

Chicago Manual of Style (16th Edition):

Rialle, Stéphanie. “Méthodologie et outils bioinformatiques d'aide à la conception de systèmes biologiques synthétiques pour de nouveaux diagnostics en santé humaine : Methodology and bioinformatics tools to design synthetic biological systems for new human health diagnosis.” 2010. Doctoral Dissertation, Université Montpellier II. Accessed May 25, 2019. http://www.theses.fr/2010MON20091.

MLA Handbook (7th Edition):

Rialle, Stéphanie. “Méthodologie et outils bioinformatiques d'aide à la conception de systèmes biologiques synthétiques pour de nouveaux diagnostics en santé humaine : Methodology and bioinformatics tools to design synthetic biological systems for new human health diagnosis.” 2010. Web. 25 May 2019.

Vancouver:

Rialle S. Méthodologie et outils bioinformatiques d'aide à la conception de systèmes biologiques synthétiques pour de nouveaux diagnostics en santé humaine : Methodology and bioinformatics tools to design synthetic biological systems for new human health diagnosis. [Internet] [Doctoral dissertation]. Université Montpellier II; 2010. [cited 2019 May 25]. Available from: http://www.theses.fr/2010MON20091.

Council of Science Editors:

Rialle S. Méthodologie et outils bioinformatiques d'aide à la conception de systèmes biologiques synthétiques pour de nouveaux diagnostics en santé humaine : Methodology and bioinformatics tools to design synthetic biological systems for new human health diagnosis. [Doctoral Dissertation]. Université Montpellier II; 2010. Available from: http://www.theses.fr/2010MON20091


University of Vienna

28. Grandl, Gerald. A directed evolution approach to engineering oxygen resistant Fe-Fe hydrogenases.

Degree: 2010, University of Vienna

Diese Arbeit stellt einen Ansatz vor eine künstliche Selektion für FeFe-Hydrogenasen in E. Coli zu entwerfen, und damit große Bibliotheken mutierter Hydrogenasen auszusortieren, mit dem… (more)

Subjects/Keywords: 42.13 Molekularbiologie; 42.30 Mikrobiologie; gerichtete Evolution / Fe-Fe Hydrogenasen / synthetische Biologie; directed Evolution / Fe-Fe hydrogenases synthetic biology

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APA (6th Edition):

Grandl, G. (2010). A directed evolution approach to engineering oxygen resistant Fe-Fe hydrogenases. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/12389/

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):

Grandl, Gerald. “A directed evolution approach to engineering oxygen resistant Fe-Fe hydrogenases.” 2010. Thesis, University of Vienna. Accessed May 25, 2019. http://othes.univie.ac.at/12389/.

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

MLA Handbook (7th Edition):

Grandl, Gerald. “A directed evolution approach to engineering oxygen resistant Fe-Fe hydrogenases.” 2010. Web. 25 May 2019.

Vancouver:

Grandl G. A directed evolution approach to engineering oxygen resistant Fe-Fe hydrogenases. [Internet] [Thesis]. University of Vienna; 2010. [cited 2019 May 25]. Available from: http://othes.univie.ac.at/12389/.

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

Council of Science Editors:

Grandl G. A directed evolution approach to engineering oxygen resistant Fe-Fe hydrogenases. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/12389/

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

29. Nguyen Quang, Nam. Utilisation du séquençage à haut débit pour la sélection et l'ingénierie des aptamères : Selection and engineering of aptamers using high-throughput sequencing.

Degree: Docteur es, Sciences de la vie et de la santé, 2017, Paris Saclay

Le SELEX est une technique d’évolution moléculaire dirigée qui permet, après plusieurs tours de sélection, d’enrichir une banque d’acides nucléiques en séquences capable de se… (more)

Subjects/Keywords: Séquençage à Haut Débit; Evolution moléculaire; Selex; Aptamères; Biologie synthétique; High-Throughput Sequencing; Molecular Evolution; Selex; Aptamers; Synthetic Biology

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

APA (6th Edition):

Nguyen Quang, N. (2017). Utilisation du séquençage à haut débit pour la sélection et l'ingénierie des aptamères : Selection and engineering of aptamers using high-throughput sequencing. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLS238

Chicago Manual of Style (16th Edition):

Nguyen Quang, Nam. “Utilisation du séquençage à haut débit pour la sélection et l'ingénierie des aptamères : Selection and engineering of aptamers using high-throughput sequencing.” 2017. Doctoral Dissertation, Paris Saclay. Accessed May 25, 2019. http://www.theses.fr/2017SACLS238.

MLA Handbook (7th Edition):

Nguyen Quang, Nam. “Utilisation du séquençage à haut débit pour la sélection et l'ingénierie des aptamères : Selection and engineering of aptamers using high-throughput sequencing.” 2017. Web. 25 May 2019.

Vancouver:

Nguyen Quang N. Utilisation du séquençage à haut débit pour la sélection et l'ingénierie des aptamères : Selection and engineering of aptamers using high-throughput sequencing. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2019 May 25]. Available from: http://www.theses.fr/2017SACLS238.

Council of Science Editors:

Nguyen Quang N. Utilisation du séquençage à haut débit pour la sélection et l'ingénierie des aptamères : Selection and engineering of aptamers using high-throughput sequencing. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLS238


University of Edinburgh

30. Moore, John Wallace. Foundation technologies in synthetic biology : tools for use in understanding plant immunity.

Degree: 2012, University of Edinburgh

 The plant hormone salicylic acid (SA) is an essential activator of plant immune responses directed against biotrophic pathogens. The transcription cofactor NPR1 (Nonexpressor of pathogenesis-… (more)

Subjects/Keywords: 571.2; synthetic biology; plant immunity; S-nitrosylation

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

APA (6th Edition):

Moore, J. W. (2012). Foundation technologies in synthetic biology : tools for use in understanding plant immunity. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/6225

Chicago Manual of Style (16th Edition):

Moore, John Wallace. “Foundation technologies in synthetic biology : tools for use in understanding plant immunity.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed May 25, 2019. http://hdl.handle.net/1842/6225.

MLA Handbook (7th Edition):

Moore, John Wallace. “Foundation technologies in synthetic biology : tools for use in understanding plant immunity.” 2012. Web. 25 May 2019.

Vancouver:

Moore JW. Foundation technologies in synthetic biology : tools for use in understanding plant immunity. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2019 May 25]. Available from: http://hdl.handle.net/1842/6225.

Council of Science Editors:

Moore JW. Foundation technologies in synthetic biology : tools for use in understanding plant immunity. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/6225

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