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You searched for subject:(site specific recombination). Showing records 1 – 16 of 16 total matches.

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Université de Montréal

1. Gustinelli, Alexandra. Système de recombinaison Xer chez Staphylococcus aureus .

Degree: 2011, Université de Montréal

 Le système de recombinaison Xer est impliqué dans la monomerisation des réplicons bactériens, comme les plasmides et les chromosomes, dans une grande variété de bactéries.… (more)

Subjects/Keywords: Recombinaison spécifique de site; tyrosine recombinase; XerD; dif; Staphylococcus aureus; Site-specific recombination

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

APA (6th Edition):

Gustinelli, A. (2011). Système de recombinaison Xer chez Staphylococcus aureus . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6958

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):

Gustinelli, Alexandra. “Système de recombinaison Xer chez Staphylococcus aureus .” 2011. Thesis, Université de Montréal. Accessed July 16, 2019. http://hdl.handle.net/1866/6958.

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

MLA Handbook (7th Edition):

Gustinelli, Alexandra. “Système de recombinaison Xer chez Staphylococcus aureus .” 2011. Web. 16 Jul 2019.

Vancouver:

Gustinelli A. Système de recombinaison Xer chez Staphylococcus aureus . [Internet] [Thesis]. Université de Montréal; 2011. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1866/6958.

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

Council of Science Editors:

Gustinelli A. Système de recombinaison Xer chez Staphylococcus aureus . [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/6958

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


Université de Montréal

2. Rezoug, Zoulikha. Le système de recombinaison site-spécifique dif/Xer de Campylobacter jejuni .

Degree: 2012, Université de Montréal

 Chez les bactéries à chromosome circulaire, la réplication peut engendrer des dimères que le système de recombinaison site-spécifique dif/Xer résout en monomères afin que la… (more)

Subjects/Keywords: Recombinaison site-spécifique; Tyrosine recombinase; Site-specific recombination; XerH; difH; Campylobacter jejuni

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APA (6th Edition):

Rezoug, Z. (2012). Le système de recombinaison site-spécifique dif/Xer de Campylobacter jejuni . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6927

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):

Rezoug, Zoulikha. “Le système de recombinaison site-spécifique dif/Xer de Campylobacter jejuni .” 2012. Thesis, Université de Montréal. Accessed July 16, 2019. http://hdl.handle.net/1866/6927.

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

MLA Handbook (7th Edition):

Rezoug, Zoulikha. “Le système de recombinaison site-spécifique dif/Xer de Campylobacter jejuni .” 2012. Web. 16 Jul 2019.

Vancouver:

Rezoug Z. Le système de recombinaison site-spécifique dif/Xer de Campylobacter jejuni . [Internet] [Thesis]. Université de Montréal; 2012. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1866/6927.

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

Council of Science Editors:

Rezoug Z. Le système de recombinaison site-spécifique dif/Xer de Campylobacter jejuni . [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/6927

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


Université de Montréal

3. Leroux, Maxime. Les systèmes Xer à une seule recombinase .

Degree: 2013, Université de Montréal

 Les dimères chromosomiques se produisant lors de la réparation de chromosomes circulaires peuvent être dommageables pour les bactéries en bloquant la ségrégation des chromosomes et… (more)

Subjects/Keywords: Recombinaison site-spécifique; tyrosine recombinase; XerS; difSL; XerH; difH; XerCD; Site-specific recombination

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APA (6th Edition):

Leroux, M. (2013). Les systèmes Xer à une seule recombinase . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/9008

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):

Leroux, Maxime. “Les systèmes Xer à une seule recombinase .” 2013. Thesis, Université de Montréal. Accessed July 16, 2019. http://hdl.handle.net/1866/9008.

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

MLA Handbook (7th Edition):

Leroux, Maxime. “Les systèmes Xer à une seule recombinase .” 2013. Web. 16 Jul 2019.

Vancouver:

Leroux M. Les systèmes Xer à une seule recombinase . [Internet] [Thesis]. Université de Montréal; 2013. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1866/9008.

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

Council of Science Editors:

Leroux M. Les systèmes Xer à une seule recombinase . [Thesis]. Université de Montréal; 2013. Available from: http://hdl.handle.net/1866/9008

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


University of Pennsylvania

4. Gibb, Bryan P S. Requirements for Catalysis in Cre Recombinase.

Degree: 2010, University of Pennsylvania

 Cre recombinase, a member of the tyrosine recombinase (YR) family of site-specific recombinases catalyzes DNA rearrangements using phosphoryl transfer chemistry that is identical to that… (more)

Subjects/Keywords: Cre; recombination; site-specific; type IB topoisomerase; tyrosine recombinase; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

Gibb, B. P. S. (2010). Requirements for Catalysis in Cre Recombinase. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/427

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):

Gibb, Bryan P S. “Requirements for Catalysis in Cre Recombinase.” 2010. Thesis, University of Pennsylvania. Accessed July 16, 2019. https://repository.upenn.edu/edissertations/427.

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

MLA Handbook (7th Edition):

Gibb, Bryan P S. “Requirements for Catalysis in Cre Recombinase.” 2010. Web. 16 Jul 2019.

Vancouver:

Gibb BPS. Requirements for Catalysis in Cre Recombinase. [Internet] [Thesis]. University of Pennsylvania; 2010. [cited 2019 Jul 16]. Available from: https://repository.upenn.edu/edissertations/427.

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

Council of Science Editors:

Gibb BPS. Requirements for Catalysis in Cre Recombinase. [Thesis]. University of Pennsylvania; 2010. Available from: https://repository.upenn.edu/edissertations/427

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


University of Waterloo

5. Brogee, Paul. Towards the Development of a ϕC31Int-Competent Sf9 Cell Line.

Degree: 2018, University of Waterloo

 The Sf9 cell line, as a component of the Baculovirus Expression Vector System (BEVS), is a popular platform for industrial-scale production of protein products. However,… (more)

Subjects/Keywords: ϕC3l Integrase; Sf9; Recombinase Mediated Cassette Exchange; Limiting Dilution; ϕC3l Recombinase; Site Specific Recombination

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APA (6th Edition):

Brogee, P. (2018). Towards the Development of a ϕC31Int-Competent Sf9 Cell Line. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/14202

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):

Brogee, Paul. “Towards the Development of a ϕC31Int-Competent Sf9 Cell Line.” 2018. Thesis, University of Waterloo. Accessed July 16, 2019. http://hdl.handle.net/10012/14202.

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

MLA Handbook (7th Edition):

Brogee, Paul. “Towards the Development of a ϕC31Int-Competent Sf9 Cell Line.” 2018. Web. 16 Jul 2019.

Vancouver:

Brogee P. Towards the Development of a ϕC31Int-Competent Sf9 Cell Line. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10012/14202.

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

Council of Science Editors:

Brogee P. Towards the Development of a ϕC31Int-Competent Sf9 Cell Line. [Thesis]. University of Waterloo; 2018. Available from: http://hdl.handle.net/10012/14202

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


Université de Montréal

6. Liu, Hua. The role of Caulobacter crescentus XerC and XerD recombinases in site-specific recombination .

Degree: 2011, Université de Montréal

 XerC et XerD, deux recombinases impliquées dans la recombinaison site spécifique, résolvent les multimères d’ADN en monomères. Cette réaction se produit au niveau du site(more)

Subjects/Keywords: Recombinasion spécifique de site; Tyrosine recombinase; XerC; XerD; dif; Caulobacter crescentus; Site-specific recombination; Tyrosine recombinase; XerC; XerD; dif; Caulobacter crescentus

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APA (6th Edition):

Liu, H. (2011). The role of Caulobacter crescentus XerC and XerD recombinases in site-specific recombination . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6856

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):

Liu, Hua. “The role of Caulobacter crescentus XerC and XerD recombinases in site-specific recombination .” 2011. Thesis, Université de Montréal. Accessed July 16, 2019. http://hdl.handle.net/1866/6856.

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

MLA Handbook (7th Edition):

Liu, Hua. “The role of Caulobacter crescentus XerC and XerD recombinases in site-specific recombination .” 2011. Web. 16 Jul 2019.

Vancouver:

Liu H. The role of Caulobacter crescentus XerC and XerD recombinases in site-specific recombination . [Internet] [Thesis]. Université de Montréal; 2011. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/1866/6856.

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

Council of Science Editors:

Liu H. The role of Caulobacter crescentus XerC and XerD recombinases in site-specific recombination . [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/6856

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


Harvard University

7. Thompson, David Brandon. Development of Methods for Protein Delivery and the Directed Evolution of Recombinases.

Degree: PhD, Biology: Medical Sciences, Division of, 2014, Harvard University

 As a class, protein-based therapeutics offer tremendous advantages over traditional small molecule drugs. Due to their sizes and folding energies, proteins are ideal for catalyzing… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Cellular biology; Cas9; directed evolution; phage-assisted continuous evolution; protein delivery; site-specific recombination; supercharged proteins

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APA (6th Edition):

Thompson, D. B. (2014). Development of Methods for Protein Delivery and the Directed Evolution of Recombinases. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:13097816

Chicago Manual of Style (16th Edition):

Thompson, David Brandon. “Development of Methods for Protein Delivery and the Directed Evolution of Recombinases.” 2014. Doctoral Dissertation, Harvard University. Accessed July 16, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13097816.

MLA Handbook (7th Edition):

Thompson, David Brandon. “Development of Methods for Protein Delivery and the Directed Evolution of Recombinases.” 2014. Web. 16 Jul 2019.

Vancouver:

Thompson DB. Development of Methods for Protein Delivery and the Directed Evolution of Recombinases. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2019 Jul 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13097816.

Council of Science Editors:

Thompson DB. Development of Methods for Protein Delivery and the Directed Evolution of Recombinases. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13097816


University of Arkansas

8. Nguyen, Linh Duy. Evaluation of the Recombination Efficiencies of FLP Proteins.

Degree: MS, 2012, University of Arkansas

Site-specific recombination systems are powerful tools for genetic modification. They have been used to integrate a transgene into a pre-defined locus and to remove… (more)

Subjects/Keywords: Biological sciences; Flp/frt; Site-specific recombination; Transgenic; Agricultural Science; Agronomy and Crop Sciences; Botany; Plant Biology; Plant Breeding and Genetics

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APA (6th Edition):

Nguyen, L. D. (2012). Evaluation of the Recombination Efficiencies of FLP Proteins. (Masters Thesis). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/651

Chicago Manual of Style (16th Edition):

Nguyen, Linh Duy. “Evaluation of the Recombination Efficiencies of FLP Proteins.” 2012. Masters Thesis, University of Arkansas. Accessed July 16, 2019. https://scholarworks.uark.edu/etd/651.

MLA Handbook (7th Edition):

Nguyen, Linh Duy. “Evaluation of the Recombination Efficiencies of FLP Proteins.” 2012. Web. 16 Jul 2019.

Vancouver:

Nguyen LD. Evaluation of the Recombination Efficiencies of FLP Proteins. [Internet] [Masters thesis]. University of Arkansas; 2012. [cited 2019 Jul 16]. Available from: https://scholarworks.uark.edu/etd/651.

Council of Science Editors:

Nguyen LD. Evaluation of the Recombination Efficiencies of FLP Proteins. [Masters Thesis]. University of Arkansas; 2012. Available from: https://scholarworks.uark.edu/etd/651


Université Paris-Sud – Paris XI

9. Gigant, Emmanuelle. La cohésion des chromatides sœurs chez Escherichia coli : Sister chromatid cohesion in Escherichia coli.

Degree: Docteur es, Biologie, 2012, Université Paris-Sud – Paris XI

Chez les bactéries, la ségrégation du chromosome est initiée durant la phase de réplication. Des expériences de time lapse, utilisées pour observer que la dynamique… (more)

Subjects/Keywords: Ségrégation du chromosome;

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APA (6th Edition):

Gigant, E. (2012). La cohésion des chromatides sœurs chez Escherichia coli : Sister chromatid cohesion in Escherichia coli. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA112347

Chicago Manual of Style (16th Edition):

Gigant, Emmanuelle. “La cohésion des chromatides sœurs chez Escherichia coli : Sister chromatid cohesion in Escherichia coli.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed July 16, 2019. http://www.theses.fr/2012PA112347.

MLA Handbook (7th Edition):

Gigant, Emmanuelle. “La cohésion des chromatides sœurs chez Escherichia coli : Sister chromatid cohesion in Escherichia coli.” 2012. Web. 16 Jul 2019.

Vancouver:

Gigant E. La cohésion des chromatides sœurs chez Escherichia coli : Sister chromatid cohesion in Escherichia coli. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2019 Jul 16]. Available from: http://www.theses.fr/2012PA112347.

Council of Science Editors:

Gigant E. La cohésion des chromatides sœurs chez Escherichia coli : Sister chromatid cohesion in Escherichia coli. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA112347

10. Delannoy, Maëlle. Rôle des facteurs de l’hôte dans le maintien des prophages chez les entérobactéries : Host factors involvement in prophage maintenance in Enterobacteriaceae.

Degree: Docteur es, Microbiologie, 2016, Aix Marseille Université

Les prophages sont des vecteurs majeurs de l’évolution des génomes bactériens et ont des rôles divers dans le processus adaptatif de leurs hôtes et peuvent… (more)

Subjects/Keywords: Prophages; Maintien lysogénie; NorV; Détoxification du NO; Recombinaison spécifique de site; Coévolution; Prophages; Lysogeny maintenance; NorV; NO detoxification; Site specific recombination; Coevolution; 579

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APA (6th Edition):

Delannoy, M. (2016). Rôle des facteurs de l’hôte dans le maintien des prophages chez les entérobactéries : Host factors involvement in prophage maintenance in Enterobacteriaceae. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4107

Chicago Manual of Style (16th Edition):

Delannoy, Maëlle. “Rôle des facteurs de l’hôte dans le maintien des prophages chez les entérobactéries : Host factors involvement in prophage maintenance in Enterobacteriaceae.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed July 16, 2019. http://www.theses.fr/2016AIXM4107.

MLA Handbook (7th Edition):

Delannoy, Maëlle. “Rôle des facteurs de l’hôte dans le maintien des prophages chez les entérobactéries : Host factors involvement in prophage maintenance in Enterobacteriaceae.” 2016. Web. 16 Jul 2019.

Vancouver:

Delannoy M. Rôle des facteurs de l’hôte dans le maintien des prophages chez les entérobactéries : Host factors involvement in prophage maintenance in Enterobacteriaceae. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2019 Jul 16]. Available from: http://www.theses.fr/2016AIXM4107.

Council of Science Editors:

Delannoy M. Rôle des facteurs de l’hôte dans le maintien des prophages chez les entérobactéries : Host factors involvement in prophage maintenance in Enterobacteriaceae. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4107


University of Arkansas

11. Akbudak, Mehmet Aydin. Applications of Site-Specific Recombination Systems in Transgene Expression and Marker Gene Removal.

Degree: PhD, 2010, University of Arkansas

Site Specific Recombination systems, such as FLP-FRT and Cre-lox, have been successfully used for site-specific gene integration and marker-gene deletion in plant systems. They… (more)

Subjects/Keywords: Biological sciences; Cre-lox; Flp-frt; Gene dosage; Marker gene removal; Rice transformation; Site-specific recombination; Transgene expression; Molecular Biology; Plant Sciences

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

APA (6th Edition):

Akbudak, M. A. (2010). Applications of Site-Specific Recombination Systems in Transgene Expression and Marker Gene Removal. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/191

Chicago Manual of Style (16th Edition):

Akbudak, Mehmet Aydin. “Applications of Site-Specific Recombination Systems in Transgene Expression and Marker Gene Removal.” 2010. Doctoral Dissertation, University of Arkansas. Accessed July 16, 2019. https://scholarworks.uark.edu/etd/191.

MLA Handbook (7th Edition):

Akbudak, Mehmet Aydin. “Applications of Site-Specific Recombination Systems in Transgene Expression and Marker Gene Removal.” 2010. Web. 16 Jul 2019.

Vancouver:

Akbudak MA. Applications of Site-Specific Recombination Systems in Transgene Expression and Marker Gene Removal. [Internet] [Doctoral dissertation]. University of Arkansas; 2010. [cited 2019 Jul 16]. Available from: https://scholarworks.uark.edu/etd/191.

Council of Science Editors:

Akbudak MA. Applications of Site-Specific Recombination Systems in Transgene Expression and Marker Gene Removal. [Doctoral Dissertation]. University of Arkansas; 2010. Available from: https://scholarworks.uark.edu/etd/191


McMaster University

12. MacLeod, Michael R. DEVELOPMENT OF AN ADVANCED GENETIC TOOLBOX TO ENABLE GENOME SCALE ENGINEERING IN SINORHIZOBIUM MELILOTI.

Degree: MSc, 2018, McMaster University

Synthetic biology has ushered in a new age of molecular biology with the aim towards practical developments in disciplines ranging from medicine, agriculture, and industry.… (more)

Subjects/Keywords: Synthetic biology; Genetic engineering; high G+C content; Sinorhizobium meliloti; multi-host shuttle vector; site-specific recombination; biotechnology; S. cerevisiae; P. tricornutum

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APA (6th Edition):

MacLeod, M. R. (2018). DEVELOPMENT OF AN ADVANCED GENETIC TOOLBOX TO ENABLE GENOME SCALE ENGINEERING IN SINORHIZOBIUM MELILOTI. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/24170

Chicago Manual of Style (16th Edition):

MacLeod, Michael R. “DEVELOPMENT OF AN ADVANCED GENETIC TOOLBOX TO ENABLE GENOME SCALE ENGINEERING IN SINORHIZOBIUM MELILOTI.” 2018. Masters Thesis, McMaster University. Accessed July 16, 2019. http://hdl.handle.net/11375/24170.

MLA Handbook (7th Edition):

MacLeod, Michael R. “DEVELOPMENT OF AN ADVANCED GENETIC TOOLBOX TO ENABLE GENOME SCALE ENGINEERING IN SINORHIZOBIUM MELILOTI.” 2018. Web. 16 Jul 2019.

Vancouver:

MacLeod MR. DEVELOPMENT OF AN ADVANCED GENETIC TOOLBOX TO ENABLE GENOME SCALE ENGINEERING IN SINORHIZOBIUM MELILOTI. [Internet] [Masters thesis]. McMaster University; 2018. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/11375/24170.

Council of Science Editors:

MacLeod MR. DEVELOPMENT OF AN ADVANCED GENETIC TOOLBOX TO ENABLE GENOME SCALE ENGINEERING IN SINORHIZOBIUM MELILOTI. [Masters Thesis]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/24170

13. Wood, Margaret. Protein/DNA interactions during site-specific recombination.

Degree: PhD, 0322, 2013, University of Illinois – Urbana-Champaign

 Bacteroides species are one of the most prevalent groups of bacteria present in the human colon. Many strains carry large, integrated elements including conjugative transposons… (more)

Subjects/Keywords: conjugative transposon; site-specific recombination; mobile genetic elements

…LAMBDA One of the best studied site-specific recombination system is that of bacteriophage… …specific recombination of the phage attP site with attB requires Int and the E. coli-encoded… …paradigmatic lambda site-specific recombination system, only Int, IHF and Xis are required for… …linA-type gene in Bacteroides spp. OTHER SITE-SPECIFIC RECOMBINATION SYSTEMS Tn916 The first… …recombination. J Biol Chem 257:9658-9662. 3. Abremski, K., and S. Gottesman. 1981. Site-specific… 

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APA (6th Edition):

Wood, M. (2013). Protein/DNA interactions during site-specific recombination. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45418

Chicago Manual of Style (16th Edition):

Wood, Margaret. “Protein/DNA interactions during site-specific recombination.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 16, 2019. http://hdl.handle.net/2142/45418.

MLA Handbook (7th Edition):

Wood, Margaret. “Protein/DNA interactions during site-specific recombination.” 2013. Web. 16 Jul 2019.

Vancouver:

Wood M. Protein/DNA interactions during site-specific recombination. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/2142/45418.

Council of Science Editors:

Wood M. Protein/DNA interactions during site-specific recombination. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45418


University of Vienna

14. Ladurner, Angela. Characterization of the inversion reaction of phiCh1 and the establishment of a transformation system for Natrialba magadii.

Degree: 2008, University of Vienna

Bis zum jetzigen Zeitpunkt wurden bakterielle und haloarchaeale Modellsysteme zur Untersuchung von phiCh1 und Nab. magadii verwendet. Durch ein Transformationsystem können Experimente auch im natürlichen… (more)

Subjects/Keywords: 42.30 Mikrobiologie; haloalkaliphile Archaea / Natrialba magadii / phiCh1 / Transformation / Site-specific Rekombinasen; haloalkaliphilic archaea / Natrialba magadii / phiCh1 / transformation / site-specific recombination

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

APA (6th Edition):

Ladurner, A. (2008). Characterization of the inversion reaction of phiCh1 and the establishment of a transformation system for Natrialba magadii. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/695/

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):

Ladurner, Angela. “Characterization of the inversion reaction of phiCh1 and the establishment of a transformation system for Natrialba magadii.” 2008. Thesis, University of Vienna. Accessed July 16, 2019. http://othes.univie.ac.at/695/.

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

MLA Handbook (7th Edition):

Ladurner, Angela. “Characterization of the inversion reaction of phiCh1 and the establishment of a transformation system for Natrialba magadii.” 2008. Web. 16 Jul 2019.

Vancouver:

Ladurner A. Characterization of the inversion reaction of phiCh1 and the establishment of a transformation system for Natrialba magadii. [Internet] [Thesis]. University of Vienna; 2008. [cited 2019 Jul 16]. Available from: http://othes.univie.ac.at/695/.

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

Council of Science Editors:

Ladurner A. Characterization of the inversion reaction of phiCh1 and the establishment of a transformation system for Natrialba magadii. [Thesis]. University of Vienna; 2008. Available from: http://othes.univie.ac.at/695/

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


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

15. Αρμακά, Μαρία. Μελέτη των κυτταρικών στόχων του παράγοντα νέκρωσης των όγκων (TNFα) σε ζωϊκά πρότυπα φλεγμονώδους πολυαρθρίτιδας.

Degree: 2008, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

 Ο ΤΝF θεωρείται ότι παίζει κεντρικό ρόλο στην ανάπτυξη της Ρευματοειδούς Αρθρίτιδας και οι αντί-TNF θεραπείες είναι πράγματι ικανοποιητικά επιτυχείς για την καταστολή της. Παρ’… (more)

Subjects/Keywords: Παράγοντας νέκρωσης όγκων; Διαγονιδιακός ποντικός; Πολυαρθρίτιδα; Νόσος Crohn; Φλεγμονώδη εντεροπάθεια τύπου Crohn; Ινοβλάστες; Ανασυνδυάση Cre; Ιστοειδικός ανασυνδυασμός; Μεταλλοπρωτεάση; Tumor necrosis factor (TNF); Transgenic mouse; Polyarthritis; Crohn's disease; Fibroblasts; Cre/LoxP site; Specific recombination; Metalloproteases

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

APA (6th Edition):

Αρμακά, . . (2008). Μελέτη των κυτταρικών στόχων του παράγοντα νέκρωσης των όγκων (TNFα) σε ζωϊκά πρότυπα φλεγμονώδους πολυαρθρίτιδας. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/18970

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):

Αρμακά, Μαρία. “Μελέτη των κυτταρικών στόχων του παράγοντα νέκρωσης των όγκων (TNFα) σε ζωϊκά πρότυπα φλεγμονώδους πολυαρθρίτιδας.” 2008. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed July 16, 2019. http://hdl.handle.net/10442/hedi/18970.

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

MLA Handbook (7th Edition):

Αρμακά, Μαρία. “Μελέτη των κυτταρικών στόχων του παράγοντα νέκρωσης των όγκων (TNFα) σε ζωϊκά πρότυπα φλεγμονώδους πολυαρθρίτιδας.” 2008. Web. 16 Jul 2019.

Vancouver:

Αρμακά . Μελέτη των κυτταρικών στόχων του παράγοντα νέκρωσης των όγκων (TNFα) σε ζωϊκά πρότυπα φλεγμονώδους πολυαρθρίτιδας. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2008. [cited 2019 Jul 16]. Available from: http://hdl.handle.net/10442/hedi/18970.

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

Council of Science Editors:

Αρμακά . Μελέτη των κυτταρικών στόχων του παράγοντα νέκρωσης των όγκων (TNFα) σε ζωϊκά πρότυπα φλεγμονώδους πολυαρθρίτιδας. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2008. Available from: http://hdl.handle.net/10442/hedi/18970

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


The Ohio State University

16. Subramaniam, Srisunder. Studies of conformational changes and dynamics accompanying substrate recognition, allostery and catalysis in bacteriophage lambda integrase.

Degree: PhD, Biophysics, 2005, The Ohio State University

 Bacteriophage lambda integrase catalyzes the site specific recombination of the viral DNA into the host genome, via a Holliday junction intermediate, and has been the… (more)

Subjects/Keywords: bacteriophage lambda integrase; site specific recombination; DNA cleaving enzymes; enzyme dynamics; enzyme catalysis; molecular recognition; substrate recognition; NMR spectroscopy; allostery; protein folding; binding-coupled protein folding

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

APA (6th Edition):

Subramaniam, S. (2005). Studies of conformational changes and dynamics accompanying substrate recognition, allostery and catalysis in bacteriophage lambda integrase. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1111655332

Chicago Manual of Style (16th Edition):

Subramaniam, Srisunder. “Studies of conformational changes and dynamics accompanying substrate recognition, allostery and catalysis in bacteriophage lambda integrase.” 2005. Doctoral Dissertation, The Ohio State University. Accessed July 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1111655332.

MLA Handbook (7th Edition):

Subramaniam, Srisunder. “Studies of conformational changes and dynamics accompanying substrate recognition, allostery and catalysis in bacteriophage lambda integrase.” 2005. Web. 16 Jul 2019.

Vancouver:

Subramaniam S. Studies of conformational changes and dynamics accompanying substrate recognition, allostery and catalysis in bacteriophage lambda integrase. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2019 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1111655332.

Council of Science Editors:

Subramaniam S. Studies of conformational changes and dynamics accompanying substrate recognition, allostery and catalysis in bacteriophage lambda integrase. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1111655332

.