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You searched for +publisher:"University of Texas – Austin" +contributor:("Jayaram, Makkuni"). Showing records 1 – 17 of 17 total matches.

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University of Texas – Austin

1. Chang, Keng-Ming. Stable propagation of the yeast 2 micron plasmid : equal segregation by hitchhiking on chromosomes.

Degree: PhD, Microbiology, 2014, University of Texas – Austin

 The 2 micron plasmid of Saccharomyces cerevisiae resides in the nucleus as an extra-chromosomal element with a steady state copy number of 40-60 per cell.… (more)

Subjects/Keywords: 2 micron plasmid; Episome; Chromosome tethering

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APA (6th Edition):

Chang, K. (2014). Stable propagation of the yeast 2 micron plasmid : equal segregation by hitchhiking on chromosomes. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/24799

Chicago Manual of Style (16th Edition):

Chang, Keng-Ming. “Stable propagation of the yeast 2 micron plasmid : equal segregation by hitchhiking on chromosomes.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/24799.

MLA Handbook (7th Edition):

Chang, Keng-Ming. “Stable propagation of the yeast 2 micron plasmid : equal segregation by hitchhiking on chromosomes.” 2014. Web. 06 May 2021.

Vancouver:

Chang K. Stable propagation of the yeast 2 micron plasmid : equal segregation by hitchhiking on chromosomes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/24799.

Council of Science Editors:

Chang K. Stable propagation of the yeast 2 micron plasmid : equal segregation by hitchhiking on chromosomes. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/24799

2. Cui, Hong, Ph. D. Role of the mitotic spindle in the equal segregation of an extrachromosomal element in Saccharomyces cerevisiae.

Degree: PhD, Microbiology, 2008, University of Texas – Austin

 The Saccharomyces cerevisiae plasmid, 2 micron circle, resides in the yeast nucleus at a high copy number. It provides no apparent growth advantage to its… (more)

Subjects/Keywords: Plasmids – Genetics; Nucleoproteins; Spindle (Cell division)

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APA (6th Edition):

Cui, Hong, P. D. (2008). Role of the mitotic spindle in the equal segregation of an extrachromosomal element in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/17846

Chicago Manual of Style (16th Edition):

Cui, Hong, Ph D. “Role of the mitotic spindle in the equal segregation of an extrachromosomal element in Saccharomyces cerevisiae.” 2008. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/17846.

MLA Handbook (7th Edition):

Cui, Hong, Ph D. “Role of the mitotic spindle in the equal segregation of an extrachromosomal element in Saccharomyces cerevisiae.” 2008. Web. 06 May 2021.

Vancouver:

Cui, Hong PD. Role of the mitotic spindle in the equal segregation of an extrachromosomal element in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2008. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/17846.

Council of Science Editors:

Cui, Hong PD. Role of the mitotic spindle in the equal segregation of an extrachromosomal element in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Texas – Austin; 2008. Available from: http://hdl.handle.net/2152/17846

3. Liu, Yen-Ting, 1980-. The segregation of native and foreign extra-chromosomal genetic elements in Saccharomyces cerevisiae : stable propagation by hitchhiking on chromosomes.

Degree: PhD, Cell and Molecular Biology, 2012, University of Texas – Austin

 The 2 micron plasmid of the budding yeast Saccharomyces cerevisiae resides in the nucleus as an extra-chromosomal element with a steady state copy number around… (more)

Subjects/Keywords: 2 micron plasmid; Viral episome; Plasmid-chromosome tethering

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APA (6th Edition):

Liu, Yen-Ting, 1. (2012). The segregation of native and foreign extra-chromosomal genetic elements in Saccharomyces cerevisiae : stable propagation by hitchhiking on chromosomes. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22068

Chicago Manual of Style (16th Edition):

Liu, Yen-Ting, 1980-. “The segregation of native and foreign extra-chromosomal genetic elements in Saccharomyces cerevisiae : stable propagation by hitchhiking on chromosomes.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/22068.

MLA Handbook (7th Edition):

Liu, Yen-Ting, 1980-. “The segregation of native and foreign extra-chromosomal genetic elements in Saccharomyces cerevisiae : stable propagation by hitchhiking on chromosomes.” 2012. Web. 06 May 2021.

Vancouver:

Liu, Yen-Ting 1. The segregation of native and foreign extra-chromosomal genetic elements in Saccharomyces cerevisiae : stable propagation by hitchhiking on chromosomes. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/22068.

Council of Science Editors:

Liu, Yen-Ting 1. The segregation of native and foreign extra-chromosomal genetic elements in Saccharomyces cerevisiae : stable propagation by hitchhiking on chromosomes. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/22068


University of Texas – Austin

4. Huang, Chu-Chun. Functional interactions of chromosome segregation factors with the 2 micron plasmid : possible evolutionary link between the plasmid portioning locus and the budding yeast centromere.

Degree: PhD, Molecular Biology, 2011, University of Texas – Austin

 The 2 micron plasmid of Saccharomyces cerevisiae is a multi-copy circular DNA genome that resides in the nucleus and exhibits nearly chromosome-like stability in host… (more)

Subjects/Keywords: Plasmid segregation; Chromosome segregation; Selfish DNA; Budding yeast; Saccharomyces; Cohesin; Cse4; Centrosomes; Plasmids

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APA (6th Edition):

Huang, C. (2011). Functional interactions of chromosome segregation factors with the 2 micron plasmid : possible evolutionary link between the plasmid portioning locus and the budding yeast centromere. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-05-2729

Chicago Manual of Style (16th Edition):

Huang, Chu-Chun. “Functional interactions of chromosome segregation factors with the 2 micron plasmid : possible evolutionary link between the plasmid portioning locus and the budding yeast centromere.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/ETD-UT-2011-05-2729.

MLA Handbook (7th Edition):

Huang, Chu-Chun. “Functional interactions of chromosome segregation factors with the 2 micron plasmid : possible evolutionary link between the plasmid portioning locus and the budding yeast centromere.” 2011. Web. 06 May 2021.

Vancouver:

Huang C. Functional interactions of chromosome segregation factors with the 2 micron plasmid : possible evolutionary link between the plasmid portioning locus and the budding yeast centromere. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-05-2729.

Council of Science Editors:

Huang C. Functional interactions of chromosome segregation factors with the 2 micron plasmid : possible evolutionary link between the plasmid portioning locus and the budding yeast centromere. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-05-2729


University of Texas – Austin

5. Chang, Hae Ryung. Defining the role of Mtf1 and N-terminal domain of Rpo41 in transcription initiation and replication.

Degree: PhD, Cell and Molecular Biology, 2012, University of Texas – Austin

 Mitochondrion is an organelle found in the eukaryotic cell. It is responsible for essential metabolic processes as well as ATP production via oxidative phosphorylation (OXPHOS).… (more)

Subjects/Keywords: Mitochondria; Transcription; RNA polymerase; Rpo41; Mtf1; Replication; Primase

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APA (6th Edition):

Chang, H. R. (2012). Defining the role of Mtf1 and N-terminal domain of Rpo41 in transcription initiation and replication. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2012-05-5860

Chicago Manual of Style (16th Edition):

Chang, Hae Ryung. “Defining the role of Mtf1 and N-terminal domain of Rpo41 in transcription initiation and replication.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/ETD-UT-2012-05-5860.

MLA Handbook (7th Edition):

Chang, Hae Ryung. “Defining the role of Mtf1 and N-terminal domain of Rpo41 in transcription initiation and replication.” 2012. Web. 06 May 2021.

Vancouver:

Chang HR. Defining the role of Mtf1 and N-terminal domain of Rpo41 in transcription initiation and replication. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/ETD-UT-2012-05-5860.

Council of Science Editors:

Chang HR. Defining the role of Mtf1 and N-terminal domain of Rpo41 in transcription initiation and replication. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/ETD-UT-2012-05-5860


University of Texas – Austin

6. -2937-0948. Mechanism of repair of Mu DNA insertions.

Degree: PhD, Cell and Molecular Biology, 2015, University of Texas – Austin

 Transposable elements are ubiquitous, occupying as much as 85% of the genome of some species, and nearly 50% of the human genome, and causing DNA… (more)

Subjects/Keywords: Mu DNA transposition; Post-integration; DNA replication and repair; Double-strand breaks

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APA (6th Edition):

-2937-0948. (2015). Mechanism of repair of Mu DNA insertions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46541

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

Chicago Manual of Style (16th Edition):

-2937-0948. “Mechanism of repair of Mu DNA insertions.” 2015. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/46541.

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

MLA Handbook (7th Edition):

-2937-0948. “Mechanism of repair of Mu DNA insertions.” 2015. Web. 06 May 2021.

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

Vancouver:

-2937-0948. Mechanism of repair of Mu DNA insertions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2015. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/46541.

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

Council of Science Editors:

-2937-0948. Mechanism of repair of Mu DNA insertions. [Doctoral Dissertation]. University of Texas – Austin; 2015. Available from: http://hdl.handle.net/2152/46541

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


University of Texas – Austin

7. Kim, Hyo Kyung. A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses.

Degree: PhD, Cell and molecular biology, 2016, University of Texas – Austin

 Bacteria use diverse nucleotide-based small molecules as second messengers to transduce various signals in their extra- and intracellular conditions, and to elicit appropriate cellular responses.… (more)

Subjects/Keywords: YfiN; C-di-GMP; FtsZ; Cell division; Envelope stress

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APA (6th Edition):

Kim, H. K. (2016). A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46436

Chicago Manual of Style (16th Edition):

Kim, Hyo Kyung. “A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/46436.

MLA Handbook (7th Edition):

Kim, Hyo Kyung. “A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses.” 2016. Web. 06 May 2021.

Vancouver:

Kim HK. A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/46436.

Council of Science Editors:

Kim HK. A diguanylate cyclase acts as a cell division inhibitor in a two-step response to reductive and envelope stresses. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/46436


University of Texas – Austin

8. Lanza, Amanda Morgan. Novel tools for engineering eukaryotic cells using a systems level approach.

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

 Engineered cellular systems are a promising avenue for production of a wide range of useful products including renewable fuels, commodity and specialty chemicals, industrial enzymes,… (more)

Subjects/Keywords: Eukaryotes; HT1080; GCN5; Codon optimization; Selection markers; Zeocin; Cre recombinase; Biotechnology; Tool development

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APA (6th Edition):

Lanza, A. M. (2013). Novel tools for engineering eukaryotic cells using a systems level approach. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30449

Chicago Manual of Style (16th Edition):

Lanza, Amanda Morgan. “Novel tools for engineering eukaryotic cells using a systems level approach.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/30449.

MLA Handbook (7th Edition):

Lanza, Amanda Morgan. “Novel tools for engineering eukaryotic cells using a systems level approach.” 2013. Web. 06 May 2021.

Vancouver:

Lanza AM. Novel tools for engineering eukaryotic cells using a systems level approach. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/30449.

Council of Science Editors:

Lanza AM. Novel tools for engineering eukaryotic cells using a systems level approach. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/30449


University of Texas – Austin

9. Fu, Qiong, Ph. D. Regulation of the activity of a budding yeast DNA damage repair enzyme Sae2.

Degree: PhD, Microbiology, 2014, University of Texas – Austin

 In response to DNA damage, many repair and signaling molecules mobilize rapidly to the sites of DNA double-strand breaks (DSBs). This network of immediate responses… (more)

Subjects/Keywords: DNA repair; Sae2

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APA (6th Edition):

Fu, Qiong, P. D. (2014). Regulation of the activity of a budding yeast DNA damage repair enzyme Sae2. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46516

Chicago Manual of Style (16th Edition):

Fu, Qiong, Ph D. “Regulation of the activity of a budding yeast DNA damage repair enzyme Sae2.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/46516.

MLA Handbook (7th Edition):

Fu, Qiong, Ph D. “Regulation of the activity of a budding yeast DNA damage repair enzyme Sae2.” 2014. Web. 06 May 2021.

Vancouver:

Fu, Qiong PD. Regulation of the activity of a budding yeast DNA damage repair enzyme Sae2. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/46516.

Council of Science Editors:

Fu, Qiong PD. Regulation of the activity of a budding yeast DNA damage repair enzyme Sae2. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/46516


University of Texas – Austin

10. Cambridge, Joshua Marc. Replication-dependent Z-ring formation (RDZ) : interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli: Interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli.

Degree: PhD, Cell and Molecular Biology, 2011, University of Texas – Austin

 Chromosome replication and cell division of Escherichia coli are coordinated with growth such that wild-type cells divide once and only once after each replication cycle.… (more)

Subjects/Keywords: E. coli; Cell division; ftsZ; Z-ring; Replication; SOS; slmA

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APA (6th Edition):

Cambridge, J. M. (2011). Replication-dependent Z-ring formation (RDZ) : interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli: Interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-12-4651

Chicago Manual of Style (16th Edition):

Cambridge, Joshua Marc. “Replication-dependent Z-ring formation (RDZ) : interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli: Interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/ETD-UT-2011-12-4651.

MLA Handbook (7th Edition):

Cambridge, Joshua Marc. “Replication-dependent Z-ring formation (RDZ) : interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli: Interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli.” 2011. Web. 06 May 2021.

Vancouver:

Cambridge JM. Replication-dependent Z-ring formation (RDZ) : interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli: Interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-12-4651.

Council of Science Editors:

Cambridge JM. Replication-dependent Z-ring formation (RDZ) : interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli: Interruption of DNA replication blocks cell division independently of nucleoid occlusion and the SOS response in E. coli. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-12-4651


University of Texas – Austin

11. Sardana, Richa. From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23.

Degree: PhD, Microbiology, 2013, University of Texas – Austin

 Ribosomes are universally conserved macromolecular machines that translate cellular genetic information into proteins. All ribosomes are com- posed of two ribonucleoprotein subunits. In eukaryotes these… (more)

Subjects/Keywords: Ribosome biogenesis; Small subunit; Central pseudoknot

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APA (6th Edition):

Sardana, R. (2013). From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/30458

Chicago Manual of Style (16th Edition):

Sardana, Richa. “From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/30458.

MLA Handbook (7th Edition):

Sardana, Richa. “From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23.” 2013. Web. 06 May 2021.

Vancouver:

Sardana R. From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/30458.

Council of Science Editors:

Sardana R. From knobs to a central pseudoknot : understanding 40S ribosomal subunit biogenesis through Bud23. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/30458


University of Texas – Austin

12. Arora, Sucheta. Role of Sae2 in repair of TopoisomeraseI-DNA conjugates.

Degree: PhD, Cell and Molecular Biology, 2016, University of Texas – Austin

 Topoisomerase inhibitors are widely used chemotherapeutic drugs. They covalently trap the target topoisomerase on DNA, which interferes with the progression of replication and transcription machinery… (more)

Subjects/Keywords: Sae2; TopoisomeraseI; Sen1; Camptothecin

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APA (6th Edition):

Arora, S. (2016). Role of Sae2 in repair of TopoisomeraseI-DNA conjugates. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68700

Chicago Manual of Style (16th Edition):

Arora, Sucheta. “Role of Sae2 in repair of TopoisomeraseI-DNA conjugates.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/68700.

MLA Handbook (7th Edition):

Arora, Sucheta. “Role of Sae2 in repair of TopoisomeraseI-DNA conjugates.” 2016. Web. 06 May 2021.

Vancouver:

Arora S. Role of Sae2 in repair of TopoisomeraseI-DNA conjugates. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/68700.

Council of Science Editors:

Arora S. Role of Sae2 in repair of TopoisomeraseI-DNA conjugates. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68700

13. -7973-9371. Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses.

Degree: PhD, Cell and Molecular Biology, 2019, University of Texas – Austin

 Yeast has long been the sine qua non of model organisms due to its experimental tractability. Recent advances in biology, such as CRISPR/Cas9 editing, promise… (more)

Subjects/Keywords: Biotechnology; Evolution

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APA (6th Edition):

-7973-9371. (2019). Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/2162

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

Chicago Manual of Style (16th Edition):

-7973-9371. “Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://dx.doi.org/10.26153/tsw/2162.

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

MLA Handbook (7th Edition):

-7973-9371. “Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses.” 2019. Web. 06 May 2021.

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

Vancouver:

-7973-9371. Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2021 May 06]. Available from: http://dx.doi.org/10.26153/tsw/2162.

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

Council of Science Editors:

-7973-9371. Yeast as a platform for synthetic biology and investigation of evolutionary hypotheses. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/2162

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


University of Texas – Austin

14. Yang, Xianmei. The stability system of the yeast 2 micron plasmid: analysis of plasmid and host encoded components.

Degree: PhD, Microbiology, 2002, University of Texas – Austin

 The work presented in this thesis aims to understand the molecular strategies used by an extrachromosomal selfish DNA element for its stable, high copy persistence.… (more)

Subjects/Keywords: Saccharomyces – Genetics; Plasmids

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APA (6th Edition):

Yang, X. (2002). The stability system of the yeast 2 micron plasmid: analysis of plasmid and host encoded components. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/1071

Chicago Manual of Style (16th Edition):

Yang, Xianmei. “The stability system of the yeast 2 micron plasmid: analysis of plasmid and host encoded components.” 2002. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/1071.

MLA Handbook (7th Edition):

Yang, Xianmei. “The stability system of the yeast 2 micron plasmid: analysis of plasmid and host encoded components.” 2002. Web. 06 May 2021.

Vancouver:

Yang X. The stability system of the yeast 2 micron plasmid: analysis of plasmid and host encoded components. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2002. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/1071.

Council of Science Editors:

Yang X. The stability system of the yeast 2 micron plasmid: analysis of plasmid and host encoded components. [Doctoral Dissertation]. University of Texas – Austin; 2002. Available from: http://hdl.handle.net/2152/1071


University of Texas – Austin

15. Pathania, Shailja. Path of DNA within Mu transpososomes: order, dynamics and topology of Mu end-enhancer interactions.

Degree: PhD, Microbiology, 2002, University of Texas – Austin

 Using a new method called ‘difference topology’, a complete topological analysis of all the intermediates in the Mu transposition pathway has been carried out. The… (more)

Subjects/Keywords: DNA – Structure; Bacteriophage mu

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APA (6th Edition):

Pathania, S. (2002). Path of DNA within Mu transpososomes: order, dynamics and topology of Mu end-enhancer interactions. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/840

Chicago Manual of Style (16th Edition):

Pathania, Shailja. “Path of DNA within Mu transpososomes: order, dynamics and topology of Mu end-enhancer interactions.” 2002. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/840.

MLA Handbook (7th Edition):

Pathania, Shailja. “Path of DNA within Mu transpososomes: order, dynamics and topology of Mu end-enhancer interactions.” 2002. Web. 06 May 2021.

Vancouver:

Pathania S. Path of DNA within Mu transpososomes: order, dynamics and topology of Mu end-enhancer interactions. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2002. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/840.

Council of Science Editors:

Pathania S. Path of DNA within Mu transpososomes: order, dynamics and topology of Mu end-enhancer interactions. [Doctoral Dissertation]. University of Texas – Austin; 2002. Available from: http://hdl.handle.net/2152/840

16. Shen, Mingjuan. Characterization of the novel endonuclease Sae2 involved in DNA end processing.

Degree: PhD, Cell and Molecular Biology, 2011, University of Texas – Austin

 At the very center of sexual reproduction is meiosis. During meiosis, the formation of meiotic Double-Strand-Breaks (DBSs) and their repair by homologous recombination are widely… (more)

Subjects/Keywords: Spo11; Sae2; DSBs; Meiotic recombination; Endonuclease

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APA (6th Edition):

Shen, M. (2011). Characterization of the novel endonuclease Sae2 involved in DNA end processing. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2011-08-4169

Chicago Manual of Style (16th Edition):

Shen, Mingjuan. “Characterization of the novel endonuclease Sae2 involved in DNA end processing.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/ETD-UT-2011-08-4169.

MLA Handbook (7th Edition):

Shen, Mingjuan. “Characterization of the novel endonuclease Sae2 involved in DNA end processing.” 2011. Web. 06 May 2021.

Vancouver:

Shen M. Characterization of the novel endonuclease Sae2 involved in DNA end processing. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4169.

Council of Science Editors:

Shen M. Characterization of the novel endonuclease Sae2 involved in DNA end processing. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/ETD-UT-2011-08-4169


University of Texas – Austin

17. Hopkins, Ben Barrett. The P. furiosus Mre11/Rad50 complex facilitates 5’ strand resection by the HerA helicase and NurA nuclease at a DNA double-strand break.

Degree: PhD, Microbiology, 2010, University of Texas – Austin

 The Mre11/Rad50 complex has been implicated in the early steps of DNA double-strand break (DSB) repair through homologous recombination in several organisms. However, the enzymatic… (more)

Subjects/Keywords: Mre11; Rad50; HerA; NurA; DNA repair; Resection; Homologous recombination; Nuclease; ATPase; Helicase; Double-strand break; Pyrococcus furiosus

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

APA (6th Edition):

Hopkins, B. B. (2010). The P. furiosus Mre11/Rad50 complex facilitates 5’ strand resection by the HerA helicase and NurA nuclease at a DNA double-strand break. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/ETD-UT-2010-05-1001

Chicago Manual of Style (16th Edition):

Hopkins, Ben Barrett. “The P. furiosus Mre11/Rad50 complex facilitates 5’ strand resection by the HerA helicase and NurA nuclease at a DNA double-strand break.” 2010. Doctoral Dissertation, University of Texas – Austin. Accessed May 06, 2021. http://hdl.handle.net/2152/ETD-UT-2010-05-1001.

MLA Handbook (7th Edition):

Hopkins, Ben Barrett. “The P. furiosus Mre11/Rad50 complex facilitates 5’ strand resection by the HerA helicase and NurA nuclease at a DNA double-strand break.” 2010. Web. 06 May 2021.

Vancouver:

Hopkins BB. The P. furiosus Mre11/Rad50 complex facilitates 5’ strand resection by the HerA helicase and NurA nuclease at a DNA double-strand break. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2010. [cited 2021 May 06]. Available from: http://hdl.handle.net/2152/ETD-UT-2010-05-1001.

Council of Science Editors:

Hopkins BB. The P. furiosus Mre11/Rad50 complex facilitates 5’ strand resection by the HerA helicase and NurA nuclease at a DNA double-strand break. [Doctoral Dissertation]. University of Texas – Austin; 2010. Available from: http://hdl.handle.net/2152/ETD-UT-2010-05-1001

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