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You searched for subject:(homologous recombination). Showing records 1 – 30 of 204 total matches.

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University of Cambridge

1. Morton, Christopher Robert. Structural and biophysical analysis of Human DNA repair protein CtIP.

Degree: PhD, 2019, University of Cambridge

 The integrity of our genome is constantly threatened by endogenous and exogenous sources of DNA damage. The successful repair of DNA lesions is necessary for… (more)

Subjects/Keywords: DNA Repair; Homologous Recombination; CtIP

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APA (6th Edition):

Morton, C. R. (2019). Structural and biophysical analysis of Human DNA repair protein CtIP. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/294355

Chicago Manual of Style (16th Edition):

Morton, Christopher Robert. “Structural and biophysical analysis of Human DNA repair protein CtIP.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 24, 2020. https://www.repository.cam.ac.uk/handle/1810/294355.

MLA Handbook (7th Edition):

Morton, Christopher Robert. “Structural and biophysical analysis of Human DNA repair protein CtIP.” 2019. Web. 24 Jan 2020.

Vancouver:

Morton CR. Structural and biophysical analysis of Human DNA repair protein CtIP. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Jan 24]. Available from: https://www.repository.cam.ac.uk/handle/1810/294355.

Council of Science Editors:

Morton CR. Structural and biophysical analysis of Human DNA repair protein CtIP. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/294355


University of Rochester

2. Stein, Alexis Ivana. The role of homologous recombination in the maintenance and repair of the mitochondrial genome.

Degree: PhD, 2017, University of Rochester

 Mitochondria are dynamic and multifunctional organelles. While the mitochondrion is traditionally thought of as the “power house” of the cell, it has many functions beyond… (more)

Subjects/Keywords: DNA repair; Mitochondria; Mitochondrial DNA; Homologous recombination

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APA (6th Edition):

Stein, A. I. (2017). The role of homologous recombination in the maintenance and repair of the mitochondrial genome. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/32256

Chicago Manual of Style (16th Edition):

Stein, Alexis Ivana. “The role of homologous recombination in the maintenance and repair of the mitochondrial genome.” 2017. Doctoral Dissertation, University of Rochester. Accessed January 24, 2020. http://hdl.handle.net/1802/32256.

MLA Handbook (7th Edition):

Stein, Alexis Ivana. “The role of homologous recombination in the maintenance and repair of the mitochondrial genome.” 2017. Web. 24 Jan 2020.

Vancouver:

Stein AI. The role of homologous recombination in the maintenance and repair of the mitochondrial genome. [Internet] [Doctoral dissertation]. University of Rochester; 2017. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1802/32256.

Council of Science Editors:

Stein AI. The role of homologous recombination in the maintenance and repair of the mitochondrial genome. [Doctoral Dissertation]. University of Rochester; 2017. Available from: http://hdl.handle.net/1802/32256


Georgia State University

3. Hamilton, Christopher. Targeting Holliday Junctions.

Degree: MS, Chemistry, 2014, Georgia State University

  Holliday junctions are formed as an intermediate during DNA recombination as the two strands come together. Recombination occurs during meiosis, and also during DNA… (more)

Subjects/Keywords: Cruciform binding ligand; Holliday junction; Homologous recombination

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APA (6th Edition):

Hamilton, C. (2014). Targeting Holliday Junctions. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/63

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):

Hamilton, Christopher. “Targeting Holliday Junctions.” 2014. Thesis, Georgia State University. Accessed January 24, 2020. https://scholarworks.gsu.edu/chemistry_theses/63.

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

MLA Handbook (7th Edition):

Hamilton, Christopher. “Targeting Holliday Junctions.” 2014. Web. 24 Jan 2020.

Vancouver:

Hamilton C. Targeting Holliday Junctions. [Internet] [Thesis]. Georgia State University; 2014. [cited 2020 Jan 24]. Available from: https://scholarworks.gsu.edu/chemistry_theses/63.

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

Council of Science Editors:

Hamilton C. Targeting Holliday Junctions. [Thesis]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/chemistry_theses/63

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


University of Dundee

4. Duro, Eris. Identification of MMS22 as a regulator of DNA repair.

Degree: PhD, 2010, University of Dundee

 Obstacles such as DNA damage can block the progression of DNA replication forks. This is a major source of genome instability that can lead to… (more)

Subjects/Keywords: 572.6; DNA damage; Genome stability; Homologous recombination; MMS22; MMS22L; NFkBIL2

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APA (6th Edition):

Duro, E. (2010). Identification of MMS22 as a regulator of DNA repair. (Doctoral Dissertation). University of Dundee. Retrieved from http://hdl.handle.net/10588/7b553aeb-8f92-492e-b16f-c4c96d36fb01

Chicago Manual of Style (16th Edition):

Duro, Eris. “Identification of MMS22 as a regulator of DNA repair.” 2010. Doctoral Dissertation, University of Dundee. Accessed January 24, 2020. http://hdl.handle.net/10588/7b553aeb-8f92-492e-b16f-c4c96d36fb01.

MLA Handbook (7th Edition):

Duro, Eris. “Identification of MMS22 as a regulator of DNA repair.” 2010. Web. 24 Jan 2020.

Vancouver:

Duro E. Identification of MMS22 as a regulator of DNA repair. [Internet] [Doctoral dissertation]. University of Dundee; 2010. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10588/7b553aeb-8f92-492e-b16f-c4c96d36fb01.

Council of Science Editors:

Duro E. Identification of MMS22 as a regulator of DNA repair. [Doctoral Dissertation]. University of Dundee; 2010. Available from: http://hdl.handle.net/10588/7b553aeb-8f92-492e-b16f-c4c96d36fb01


University of South Carolina

5. Li, Shen. Mismatch Tolerance during Homologous Recombination in Mammalian Cells.

Degree: PhD, Biological Sciences, 2017, University of South Carolina

Homologous recombination (HR) serves critical roles in DNA repair to maintain genome stability, and the malfunction of HR contributes to carcinogenesis and cancer development.… (more)

Subjects/Keywords: Biology; Life Sciences; Mammalian Cells; Tolerance; Homologous Recombination

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APA (6th Edition):

Li, S. (2017). Mismatch Tolerance during Homologous Recombination in Mammalian Cells. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/4133

Chicago Manual of Style (16th Edition):

Li, Shen. “Mismatch Tolerance during Homologous Recombination in Mammalian Cells.” 2017. Doctoral Dissertation, University of South Carolina. Accessed January 24, 2020. https://scholarcommons.sc.edu/etd/4133.

MLA Handbook (7th Edition):

Li, Shen. “Mismatch Tolerance during Homologous Recombination in Mammalian Cells.” 2017. Web. 24 Jan 2020.

Vancouver:

Li S. Mismatch Tolerance during Homologous Recombination in Mammalian Cells. [Internet] [Doctoral dissertation]. University of South Carolina; 2017. [cited 2020 Jan 24]. Available from: https://scholarcommons.sc.edu/etd/4133.

Council of Science Editors:

Li S. Mismatch Tolerance during Homologous Recombination in Mammalian Cells. [Doctoral Dissertation]. University of South Carolina; 2017. Available from: https://scholarcommons.sc.edu/etd/4133


University of Pennsylvania

6. Sivanand, Sharanya. Linking Metabolism With Dna Repair: Role Of Atp-Citrate Lyase.

Degree: 2017, University of Pennsylvania

 Maintaining genomic integrity and sustaining bioenergetics are both fundamental biological functions of normal proliferating cells. Crosstalk between metabolic and DNA repair pathways are poorly understood.… (more)

Subjects/Keywords: Acetylation; Acetyl-CoA; ACLY; DNA repair; Homologous recombination; Metabolism; Biology

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APA (6th Edition):

Sivanand, S. (2017). Linking Metabolism With Dna Repair: Role Of Atp-Citrate Lyase. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2854

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):

Sivanand, Sharanya. “Linking Metabolism With Dna Repair: Role Of Atp-Citrate Lyase.” 2017. Thesis, University of Pennsylvania. Accessed January 24, 2020. https://repository.upenn.edu/edissertations/2854.

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

MLA Handbook (7th Edition):

Sivanand, Sharanya. “Linking Metabolism With Dna Repair: Role Of Atp-Citrate Lyase.” 2017. Web. 24 Jan 2020.

Vancouver:

Sivanand S. Linking Metabolism With Dna Repair: Role Of Atp-Citrate Lyase. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Jan 24]. Available from: https://repository.upenn.edu/edissertations/2854.

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

Council of Science Editors:

Sivanand S. Linking Metabolism With Dna Repair: Role Of Atp-Citrate Lyase. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2854

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


University of Pennsylvania

7. Cho, Nam Woo. Homologous Recombination-Directed Mechanisms of Alternative Lengthening of Telomeres.

Degree: 2015, University of Pennsylvania

 Telomere length maintenance is a requisite feature of cellular immortalization and a hallmark of human cancer. While most human cancers express telomerase activity, ∼10%-15% employ… (more)

Subjects/Keywords: Alternative Lengthening of Telomeres; Homologous recombination; Cell Biology; Molecular Biology

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APA (6th Edition):

Cho, N. W. (2015). Homologous Recombination-Directed Mechanisms of Alternative Lengthening of Telomeres. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1655

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):

Cho, Nam Woo. “Homologous Recombination-Directed Mechanisms of Alternative Lengthening of Telomeres.” 2015. Thesis, University of Pennsylvania. Accessed January 24, 2020. https://repository.upenn.edu/edissertations/1655.

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

MLA Handbook (7th Edition):

Cho, Nam Woo. “Homologous Recombination-Directed Mechanisms of Alternative Lengthening of Telomeres.” 2015. Web. 24 Jan 2020.

Vancouver:

Cho NW. Homologous Recombination-Directed Mechanisms of Alternative Lengthening of Telomeres. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2020 Jan 24]. Available from: https://repository.upenn.edu/edissertations/1655.

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

Council of Science Editors:

Cho NW. Homologous Recombination-Directed Mechanisms of Alternative Lengthening of Telomeres. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1655

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


The Ohio State University

8. Amunugama, Ravindra Bandara. Insights into Regulation of Human RAD51 Nucleoprotein Filament Activity During Homologous Recombination.

Degree: PhD, Biophysics, 2011, The Ohio State University

Homologous recombination (HR) is a mechanistically conserved pathway that occurs during meiosis and following the formation of DNA double strand breaks (DSBs) induced by exogenous… (more)

Subjects/Keywords: Biochemistry; Biophysics; Molecular Biology; Homologous Recombination; DNA Repair; RAD51; RAD51 paralogs

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APA (6th Edition):

Amunugama, R. B. (2011). Insights into Regulation of Human RAD51 Nucleoprotein Filament Activity During Homologous Recombination. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1321984760

Chicago Manual of Style (16th Edition):

Amunugama, Ravindra Bandara. “Insights into Regulation of Human RAD51 Nucleoprotein Filament Activity During Homologous Recombination.” 2011. Doctoral Dissertation, The Ohio State University. Accessed January 24, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1321984760.

MLA Handbook (7th Edition):

Amunugama, Ravindra Bandara. “Insights into Regulation of Human RAD51 Nucleoprotein Filament Activity During Homologous Recombination.” 2011. Web. 24 Jan 2020.

Vancouver:

Amunugama RB. Insights into Regulation of Human RAD51 Nucleoprotein Filament Activity During Homologous Recombination. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Jan 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1321984760.

Council of Science Editors:

Amunugama RB. Insights into Regulation of Human RAD51 Nucleoprotein Filament Activity During Homologous Recombination. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1321984760


University of Toledo Health Science Campus

9. Smiraldo, Phillip G. The Rad51d DNA Repair Gene is Required for Chromosome and Telomore Stability in Mammalian Cells.

Degree: PhD, College of Graduate Studies, 2006, University of Toledo Health Science Campus

 The process of homologous genetic recombination is essential for increasing genetic diversity, maintaining chromosome and telomere structure, and repairing DNA damage. A homozygous targeted disruption… (more)

Subjects/Keywords: DNA Repair; Homologous Recombination; Telomere

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APA (6th Edition):

Smiraldo, P. G. (2006). The Rad51d DNA Repair Gene is Required for Chromosome and Telomore Stability in Mammalian Cells. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1146675938

Chicago Manual of Style (16th Edition):

Smiraldo, Phillip G. “The Rad51d DNA Repair Gene is Required for Chromosome and Telomore Stability in Mammalian Cells.” 2006. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed January 24, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1146675938.

MLA Handbook (7th Edition):

Smiraldo, Phillip G. “The Rad51d DNA Repair Gene is Required for Chromosome and Telomore Stability in Mammalian Cells.” 2006. Web. 24 Jan 2020.

Vancouver:

Smiraldo PG. The Rad51d DNA Repair Gene is Required for Chromosome and Telomore Stability in Mammalian Cells. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2006. [cited 2020 Jan 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1146675938.

Council of Science Editors:

Smiraldo PG. The Rad51d DNA Repair Gene is Required for Chromosome and Telomore Stability in Mammalian Cells. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1146675938


Penn State University

10. Quan, Li. FUNCTIONAL AND EVOLUTIONARY ANALYSES OF KINESIN AND MEIOTIC GENES IN PLANTS.

Degree: PhD, Biology, 2008, Penn State University

 Meiosis is an essential step in sexual reproduction but only a small number of genes are known to be needed for plant meiosis. In addition,… (more)

Subjects/Keywords: kinesin; meiosis; spindle; gene duplication; homologous recombination; functional divergence

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APA (6th Edition):

Quan, L. (2008). FUNCTIONAL AND EVOLUTIONARY ANALYSES OF KINESIN AND MEIOTIC GENES IN PLANTS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8612

Chicago Manual of Style (16th Edition):

Quan, Li. “FUNCTIONAL AND EVOLUTIONARY ANALYSES OF KINESIN AND MEIOTIC GENES IN PLANTS.” 2008. Doctoral Dissertation, Penn State University. Accessed January 24, 2020. https://etda.libraries.psu.edu/catalog/8612.

MLA Handbook (7th Edition):

Quan, Li. “FUNCTIONAL AND EVOLUTIONARY ANALYSES OF KINESIN AND MEIOTIC GENES IN PLANTS.” 2008. Web. 24 Jan 2020.

Vancouver:

Quan L. FUNCTIONAL AND EVOLUTIONARY ANALYSES OF KINESIN AND MEIOTIC GENES IN PLANTS. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2020 Jan 24]. Available from: https://etda.libraries.psu.edu/catalog/8612.

Council of Science Editors:

Quan L. FUNCTIONAL AND EVOLUTIONARY ANALYSES OF KINESIN AND MEIOTIC GENES IN PLANTS. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8612


University of Oxford

11. Nguyen, Michael Ong. Investigating the molecular mechanism of replication restart in fission yeast.

Degree: PhD, 2014, University of Oxford

 Successful replication of the genome during each cell cycle requires that every replication fork merge with its opposing fork. However, lesions in the template DNA… (more)

Subjects/Keywords: 572.8; Biochemistry; DNA replication; homologous recombination; replication fork barrier

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APA (6th Edition):

Nguyen, M. O. (2014). Investigating the molecular mechanism of replication restart in fission yeast. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:b90fff59-d5b7-43b2-b648-61c0bc977ee9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618528

Chicago Manual of Style (16th Edition):

Nguyen, Michael Ong. “Investigating the molecular mechanism of replication restart in fission yeast.” 2014. Doctoral Dissertation, University of Oxford. Accessed January 24, 2020. http://ora.ox.ac.uk/objects/uuid:b90fff59-d5b7-43b2-b648-61c0bc977ee9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618528.

MLA Handbook (7th Edition):

Nguyen, Michael Ong. “Investigating the molecular mechanism of replication restart in fission yeast.” 2014. Web. 24 Jan 2020.

Vancouver:

Nguyen MO. Investigating the molecular mechanism of replication restart in fission yeast. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jan 24]. Available from: http://ora.ox.ac.uk/objects/uuid:b90fff59-d5b7-43b2-b648-61c0bc977ee9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618528.

Council of Science Editors:

Nguyen MO. Investigating the molecular mechanism of replication restart in fission yeast. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:b90fff59-d5b7-43b2-b648-61c0bc977ee9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618528

12. Eppink, Berina. The cellular process of homologous recombination and its applications in cancer biology.

Degree: Department of Molecular Genetics, 2010, Erasmus University Medical Center

 textabstractThe structure of DNA and subsequently the integrity of the genetic code are constantly threatened by numerous endogenous and exogenous DNA damaging agents. Restoration of… (more)

Subjects/Keywords: DNA repair; Homologous recombination; cancer

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APA (6th Edition):

Eppink, B. (2010). The cellular process of homologous recombination and its applications in cancer biology. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/26722

Chicago Manual of Style (16th Edition):

Eppink, Berina. “The cellular process of homologous recombination and its applications in cancer biology.” 2010. Doctoral Dissertation, Erasmus University Medical Center. Accessed January 24, 2020. http://hdl.handle.net/1765/26722.

MLA Handbook (7th Edition):

Eppink, Berina. “The cellular process of homologous recombination and its applications in cancer biology.” 2010. Web. 24 Jan 2020.

Vancouver:

Eppink B. The cellular process of homologous recombination and its applications in cancer biology. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2010. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1765/26722.

Council of Science Editors:

Eppink B. The cellular process of homologous recombination and its applications in cancer biology. [Doctoral Dissertation]. Erasmus University Medical Center; 2010. Available from: http://hdl.handle.net/1765/26722

13. Holthausen, Thomas. Mechanism of Genome Protection by Homologous Recombination Repair: A single molecule DNA-protein interaction study.

Degree: 2012, Erasmus University Medical Center

 textabstractChanges in our hereditary information are welcome in terms of generating diversity and driving evolution of the species. At the same time the integrity of… (more)

Subjects/Keywords: DNA repair; homologous recombination

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APA (6th Edition):

Holthausen, T. (2012). Mechanism of Genome Protection by Homologous Recombination Repair: A single molecule DNA-protein interaction study. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/31353

Chicago Manual of Style (16th Edition):

Holthausen, Thomas. “Mechanism of Genome Protection by Homologous Recombination Repair: A single molecule DNA-protein interaction study.” 2012. Doctoral Dissertation, Erasmus University Medical Center. Accessed January 24, 2020. http://hdl.handle.net/1765/31353.

MLA Handbook (7th Edition):

Holthausen, Thomas. “Mechanism of Genome Protection by Homologous Recombination Repair: A single molecule DNA-protein interaction study.” 2012. Web. 24 Jan 2020.

Vancouver:

Holthausen T. Mechanism of Genome Protection by Homologous Recombination Repair: A single molecule DNA-protein interaction study. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2012. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1765/31353.

Council of Science Editors:

Holthausen T. Mechanism of Genome Protection by Homologous Recombination Repair: A single molecule DNA-protein interaction study. [Doctoral Dissertation]. Erasmus University Medical Center; 2012. Available from: http://hdl.handle.net/1765/31353


Boston University

14. O'Connor, Kevin William. Molecular determinants of sensitivity to poly(ADP-ribose) polymerase inhibitors in epithelial ovarian cancer.

Degree: MS, Medical Sciences, 2016, Boston University

 Less than half of patients with epithelial ovarian cancer (EOC) survive five years following diagnosis, underscoring the imperative need for improved treatment. Many patients, including… (more)

Subjects/Keywords: Oncology; PARP inhibitors; Homologous recombination; Ovarian cancer; Synthetic lethality

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APA (6th Edition):

O'Connor, K. W. (2016). Molecular determinants of sensitivity to poly(ADP-ribose) polymerase inhibitors in epithelial ovarian cancer. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16827

Chicago Manual of Style (16th Edition):

O'Connor, Kevin William. “Molecular determinants of sensitivity to poly(ADP-ribose) polymerase inhibitors in epithelial ovarian cancer.” 2016. Masters Thesis, Boston University. Accessed January 24, 2020. http://hdl.handle.net/2144/16827.

MLA Handbook (7th Edition):

O'Connor, Kevin William. “Molecular determinants of sensitivity to poly(ADP-ribose) polymerase inhibitors in epithelial ovarian cancer.” 2016. Web. 24 Jan 2020.

Vancouver:

O'Connor KW. Molecular determinants of sensitivity to poly(ADP-ribose) polymerase inhibitors in epithelial ovarian cancer. [Internet] [Masters thesis]. Boston University; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/2144/16827.

Council of Science Editors:

O'Connor KW. Molecular determinants of sensitivity to poly(ADP-ribose) polymerase inhibitors in epithelial ovarian cancer. [Masters Thesis]. Boston University; 2016. Available from: http://hdl.handle.net/2144/16827


Cornell University

15. Bozza, Christopher. Mapping And Cytological Characterization Of Maize Meiotic Mutants Segii And Dsycs .

Degree: 2012, Cornell University

Homologous pairing during meiosis is an important process for the fidelity of recombination and chromosome segregation. The activity of homologous pairing has been linked to… (more)

Subjects/Keywords: Meiosis; Homologous Pairing; chiasmata; recombination; segII; dsyCS; sei; Crossover homeostasis

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APA (6th Edition):

Bozza, C. (2012). Mapping And Cytological Characterization Of Maize Meiotic Mutants Segii And Dsycs . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/31407

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):

Bozza, Christopher. “Mapping And Cytological Characterization Of Maize Meiotic Mutants Segii And Dsycs .” 2012. Thesis, Cornell University. Accessed January 24, 2020. http://hdl.handle.net/1813/31407.

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

MLA Handbook (7th Edition):

Bozza, Christopher. “Mapping And Cytological Characterization Of Maize Meiotic Mutants Segii And Dsycs .” 2012. Web. 24 Jan 2020.

Vancouver:

Bozza C. Mapping And Cytological Characterization Of Maize Meiotic Mutants Segii And Dsycs . [Internet] [Thesis]. Cornell University; 2012. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1813/31407.

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

Council of Science Editors:

Bozza C. Mapping And Cytological Characterization Of Maize Meiotic Mutants Segii And Dsycs . [Thesis]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31407

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


California State University – San Bernardino

16. Neherin, Kashfia. EXAMINING THE ROLE OF THE XAB2 PROTEIN IN HOMOLOGOUS RECOMBINATION.

Degree: MSin Biology, Biology, 2015, California State University – San Bernardino

  DNA double strand break (DSB) repair is critical to maintain genomic integrity and cell viability. DSBs can occur during the course of cell cycle… (more)

Subjects/Keywords: Homologous recombination; XAB2; Double strand break; DNA damage; Molecular Genetics

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APA (6th Edition):

Neherin, K. (2015). EXAMINING THE ROLE OF THE XAB2 PROTEIN IN HOMOLOGOUS RECOMBINATION. (Thesis). California State University – San Bernardino. Retrieved from https://scholarworks.lib.csusb.edu/etd/153

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):

Neherin, Kashfia. “EXAMINING THE ROLE OF THE XAB2 PROTEIN IN HOMOLOGOUS RECOMBINATION.” 2015. Thesis, California State University – San Bernardino. Accessed January 24, 2020. https://scholarworks.lib.csusb.edu/etd/153.

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

MLA Handbook (7th Edition):

Neherin, Kashfia. “EXAMINING THE ROLE OF THE XAB2 PROTEIN IN HOMOLOGOUS RECOMBINATION.” 2015. Web. 24 Jan 2020.

Vancouver:

Neherin K. EXAMINING THE ROLE OF THE XAB2 PROTEIN IN HOMOLOGOUS RECOMBINATION. [Internet] [Thesis]. California State University – San Bernardino; 2015. [cited 2020 Jan 24]. Available from: https://scholarworks.lib.csusb.edu/etd/153.

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

Council of Science Editors:

Neherin K. EXAMINING THE ROLE OF THE XAB2 PROTEIN IN HOMOLOGOUS RECOMBINATION. [Thesis]. California State University – San Bernardino; 2015. Available from: https://scholarworks.lib.csusb.edu/etd/153

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


University of Dundee

17. Duro, Eris. Identification of MMS22 as a regulator of DNA repair.

Degree: PhD, 2010, University of Dundee

 Obstacles such as DNA damage can block the progression of DNA replication forks. This is a major source of genome instability that can lead to… (more)

Subjects/Keywords: 572.6; DNA damage; Genome stability; Homologous recombination; MMS22; MMS22L; NFkBIL2

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APA (6th Edition):

Duro, E. (2010). Identification of MMS22 as a regulator of DNA repair. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/7b553aeb-8f92-492e-b16f-c4c96d36fb01 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578744

Chicago Manual of Style (16th Edition):

Duro, Eris. “Identification of MMS22 as a regulator of DNA repair.” 2010. Doctoral Dissertation, University of Dundee. Accessed January 24, 2020. https://discovery.dundee.ac.uk/en/studentTheses/7b553aeb-8f92-492e-b16f-c4c96d36fb01 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578744.

MLA Handbook (7th Edition):

Duro, Eris. “Identification of MMS22 as a regulator of DNA repair.” 2010. Web. 24 Jan 2020.

Vancouver:

Duro E. Identification of MMS22 as a regulator of DNA repair. [Internet] [Doctoral dissertation]. University of Dundee; 2010. [cited 2020 Jan 24]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/7b553aeb-8f92-492e-b16f-c4c96d36fb01 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578744.

Council of Science Editors:

Duro E. Identification of MMS22 as a regulator of DNA repair. [Doctoral Dissertation]. University of Dundee; 2010. Available from: https://discovery.dundee.ac.uk/en/studentTheses/7b553aeb-8f92-492e-b16f-c4c96d36fb01 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578744


University of Edinburgh

18. Azeroglu, Benura. DNA synthesis during double-strand break repair in Escherichia coli.

Degree: PhD, 2015, University of Edinburgh

 Efficient and accurate repair of DNA double strand breaks (DSBs) is required to maintain genomic stability in both eukaryotes and prokaryotes. In Escherichia coli, DSBs… (more)

Subjects/Keywords: 572.8; DNA synthesis; RecG; double-strand break repair; PriA; homologous recombination

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APA (6th Edition):

Azeroglu, B. (2015). DNA synthesis during double-strand break repair in Escherichia coli. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/16213

Chicago Manual of Style (16th Edition):

Azeroglu, Benura. “DNA synthesis during double-strand break repair in Escherichia coli.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed January 24, 2020. http://hdl.handle.net/1842/16213.

MLA Handbook (7th Edition):

Azeroglu, Benura. “DNA synthesis during double-strand break repair in Escherichia coli.” 2015. Web. 24 Jan 2020.

Vancouver:

Azeroglu B. DNA synthesis during double-strand break repair in Escherichia coli. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1842/16213.

Council of Science Editors:

Azeroglu B. DNA synthesis during double-strand break repair in Escherichia coli. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/16213


Brandeis University

19. Wang, Ruoxi. The Role of Chromosome Organization in DNA Double-Strand Break Repair.

Degree: 2016, Brandeis University

 3D nuclear architecture is a key factor in regulating many cellular processes. Here, based on the published haploid yeast chromosome conformation capture data, we investigated… (more)

Subjects/Keywords: chromosome conformation; double-strand break repair; homology search; homologous recombination

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APA (6th Edition):

Wang, R. (2016). The Role of Chromosome Organization in DNA Double-Strand Break Repair. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/32360

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):

Wang, Ruoxi. “The Role of Chromosome Organization in DNA Double-Strand Break Repair.” 2016. Thesis, Brandeis University. Accessed January 24, 2020. http://hdl.handle.net/10192/32360.

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

MLA Handbook (7th Edition):

Wang, Ruoxi. “The Role of Chromosome Organization in DNA Double-Strand Break Repair.” 2016. Web. 24 Jan 2020.

Vancouver:

Wang R. The Role of Chromosome Organization in DNA Double-Strand Break Repair. [Internet] [Thesis]. Brandeis University; 2016. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10192/32360.

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

Council of Science Editors:

Wang R. The Role of Chromosome Organization in DNA Double-Strand Break Repair. [Thesis]. Brandeis University; 2016. Available from: http://hdl.handle.net/10192/32360

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


University of Toronto

20. Wei, Chun Hua. Exploring the Role of HOP2 in the Double Strand Break Repair Pathway beyond Meiosis in Arabidopsis thaliana.

Degree: 2018, University of Toronto

The purpose of this study was to investigate the role of HOP2 protein in non-meiotic cells in Arabidopsis. HOP2 is known to be important to… (more)

Subjects/Keywords: Arabidopsis thaliana; DSB repair; Homologous Recombination; HOP2; Meiosis; Mitosis; 0369

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

APA (6th Edition):

Wei, C. H. (2018). Exploring the Role of HOP2 in the Double Strand Break Repair Pathway beyond Meiosis in Arabidopsis thaliana. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91476

Chicago Manual of Style (16th Edition):

Wei, Chun Hua. “Exploring the Role of HOP2 in the Double Strand Break Repair Pathway beyond Meiosis in Arabidopsis thaliana.” 2018. Masters Thesis, University of Toronto. Accessed January 24, 2020. http://hdl.handle.net/1807/91476.

MLA Handbook (7th Edition):

Wei, Chun Hua. “Exploring the Role of HOP2 in the Double Strand Break Repair Pathway beyond Meiosis in Arabidopsis thaliana.” 2018. Web. 24 Jan 2020.

Vancouver:

Wei CH. Exploring the Role of HOP2 in the Double Strand Break Repair Pathway beyond Meiosis in Arabidopsis thaliana. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/1807/91476.

Council of Science Editors:

Wei CH. Exploring the Role of HOP2 in the Double Strand Break Repair Pathway beyond Meiosis in Arabidopsis thaliana. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91476

21. Dai, Dingli. Caractérisation des interactions physiques et fonctionnelles entre le facteur d’assemblage de la chromatine, CAF-1, et des facteurs de la recombinaison homologue au cours de la réparation de l’ADN : Characterization of Physical and Functional Interactions Between the Chromatin Assembly Factor 1, CAF-1, and Homologous Recombination Factors During DNA Repair.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Paris Saclay

L’ADN est constamment exposé à des insultes génotoxiques endogènes et exogènes. Plusieurs mécanismes de réparations de l’ADN sont mis en œuvre pour préserver la stabilité… (more)

Subjects/Keywords: Recombinaison homologue; Réparation de l'ADN; Chromatine; Homologous recombination; DNA repair; Chromatin

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

APA (6th Edition):

Dai, D. (2018). Caractérisation des interactions physiques et fonctionnelles entre le facteur d’assemblage de la chromatine, CAF-1, et des facteurs de la recombinaison homologue au cours de la réparation de l’ADN : Characterization of Physical and Functional Interactions Between the Chromatin Assembly Factor 1, CAF-1, and Homologous Recombination Factors During DNA Repair. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS498

Chicago Manual of Style (16th Edition):

Dai, Dingli. “Caractérisation des interactions physiques et fonctionnelles entre le facteur d’assemblage de la chromatine, CAF-1, et des facteurs de la recombinaison homologue au cours de la réparation de l’ADN : Characterization of Physical and Functional Interactions Between the Chromatin Assembly Factor 1, CAF-1, and Homologous Recombination Factors During DNA Repair.” 2018. Doctoral Dissertation, Paris Saclay. Accessed January 24, 2020. http://www.theses.fr/2018SACLS498.

MLA Handbook (7th Edition):

Dai, Dingli. “Caractérisation des interactions physiques et fonctionnelles entre le facteur d’assemblage de la chromatine, CAF-1, et des facteurs de la recombinaison homologue au cours de la réparation de l’ADN : Characterization of Physical and Functional Interactions Between the Chromatin Assembly Factor 1, CAF-1, and Homologous Recombination Factors During DNA Repair.” 2018. Web. 24 Jan 2020.

Vancouver:

Dai D. Caractérisation des interactions physiques et fonctionnelles entre le facteur d’assemblage de la chromatine, CAF-1, et des facteurs de la recombinaison homologue au cours de la réparation de l’ADN : Characterization of Physical and Functional Interactions Between the Chromatin Assembly Factor 1, CAF-1, and Homologous Recombination Factors During DNA Repair. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2020 Jan 24]. Available from: http://www.theses.fr/2018SACLS498.

Council of Science Editors:

Dai D. Caractérisation des interactions physiques et fonctionnelles entre le facteur d’assemblage de la chromatine, CAF-1, et des facteurs de la recombinaison homologue au cours de la réparation de l’ADN : Characterization of Physical and Functional Interactions Between the Chromatin Assembly Factor 1, CAF-1, and Homologous Recombination Factors During DNA Repair. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS498


University of Guelph

22. Cealic, Iulia. Role of the Breast Cancer Susceptibility 2 BRC Repeats in Homologous Recombination .

Degree: 2013, University of Guelph

Homologous recombination (HR) is a faithful mechanism for the repair of double-stranded DNA breaks (DSBs) and plays a critical role in maintaining the integrity of… (more)

Subjects/Keywords: BRCA2; BRC repeats; Homologous recombination; Gene targeting; Rad51

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APA (6th Edition):

Cealic, I. (2013). Role of the Breast Cancer Susceptibility 2 BRC Repeats in Homologous Recombination . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5259

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):

Cealic, Iulia. “Role of the Breast Cancer Susceptibility 2 BRC Repeats in Homologous Recombination .” 2013. Thesis, University of Guelph. Accessed January 24, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5259.

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

MLA Handbook (7th Edition):

Cealic, Iulia. “Role of the Breast Cancer Susceptibility 2 BRC Repeats in Homologous Recombination .” 2013. Web. 24 Jan 2020.

Vancouver:

Cealic I. Role of the Breast Cancer Susceptibility 2 BRC Repeats in Homologous Recombination . [Internet] [Thesis]. University of Guelph; 2013. [cited 2020 Jan 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5259.

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

Council of Science Editors:

Cealic I. Role of the Breast Cancer Susceptibility 2 BRC Repeats in Homologous Recombination . [Thesis]. University of Guelph; 2013. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/5259

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


University of Guelph

23. Knapp, Jennifer. Investigating the Role of Rad51 in Mammalian Ectopic Homologous Recombination.

Degree: 2013, University of Guelph

 DNA damage occurs through endogenous and exogenous sources, and can lead to stalled replication forks, genetic disorders, cancer, and cell death. Homologous recombination (HR) is… (more)

Subjects/Keywords: Ectopic homologous recombination; Murine hybridoma cells; Rad51; DNA damage; Gene Targeting

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APA (6th Edition):

Knapp, J. (2013). Investigating the Role of Rad51 in Mammalian Ectopic Homologous Recombination. (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7280

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):

Knapp, Jennifer. “Investigating the Role of Rad51 in Mammalian Ectopic Homologous Recombination.” 2013. Thesis, University of Guelph. Accessed January 24, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7280.

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

MLA Handbook (7th Edition):

Knapp, Jennifer. “Investigating the Role of Rad51 in Mammalian Ectopic Homologous Recombination.” 2013. Web. 24 Jan 2020.

Vancouver:

Knapp J. Investigating the Role of Rad51 in Mammalian Ectopic Homologous Recombination. [Internet] [Thesis]. University of Guelph; 2013. [cited 2020 Jan 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7280.

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

Council of Science Editors:

Knapp J. Investigating the Role of Rad51 in Mammalian Ectopic Homologous Recombination. [Thesis]. University of Guelph; 2013. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7280

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


University of Guelph

24. Mundia, Maureen. Analysis of the Genetic Requirements for Rad51-Mediated 3’ Polymerization during DNA Repair by Homologous Recombination .

Degree: 2016, University of Guelph

 Unrepaired double-strand breaks (DSBs) disrupt the integrity of DNA and may lead to genome instability, which has been linked to aging and many human diseases,… (more)

Subjects/Keywords: DNA repair; Homologous recombination; 3' polymerization; mouse hybridoma; Rad51; BRCA2

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APA (6th Edition):

Mundia, M. (2016). Analysis of the Genetic Requirements for Rad51-Mediated 3’ Polymerization during DNA Repair by Homologous Recombination . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9672

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):

Mundia, Maureen. “Analysis of the Genetic Requirements for Rad51-Mediated 3’ Polymerization during DNA Repair by Homologous Recombination .” 2016. Thesis, University of Guelph. Accessed January 24, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9672.

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

MLA Handbook (7th Edition):

Mundia, Maureen. “Analysis of the Genetic Requirements for Rad51-Mediated 3’ Polymerization during DNA Repair by Homologous Recombination .” 2016. Web. 24 Jan 2020.

Vancouver:

Mundia M. Analysis of the Genetic Requirements for Rad51-Mediated 3’ Polymerization during DNA Repair by Homologous Recombination . [Internet] [Thesis]. University of Guelph; 2016. [cited 2020 Jan 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9672.

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

Council of Science Editors:

Mundia M. Analysis of the Genetic Requirements for Rad51-Mediated 3’ Polymerization during DNA Repair by Homologous Recombination . [Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9672

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

25. Desai, Vatsal. Homology Requirements in Mammalian Early Homologous Recombination .

Degree: 2013, University of Guelph

Homologous recombination (HR) is a precise mechanism for repairing harmful DNA double-strand breaks. The process has been extensively studied in microbial species leading to identification… (more)

Subjects/Keywords: Homologous recombination; 3' extension

homologous recombination IgH immunoglobulin heavy chain IgM immunoglobulin M kb kilobase LB… …homology for repair. Homologous recombination (HR) is used to repair DSBs with a… …joining (NHEJ) pathway and the homologous recombination (HR) pathway. The… …Homologous recombination mechanisms Homologous recombination represents a second, essential DSB… …homologous recombination designation and these are used in different circumstances. In the mitotic… 

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APA (6th Edition):

Desai, V. (2013). Homology Requirements in Mammalian Early Homologous Recombination . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6593

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):

Desai, Vatsal. “Homology Requirements in Mammalian Early Homologous Recombination .” 2013. Thesis, University of Guelph. Accessed January 24, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6593.

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

MLA Handbook (7th Edition):

Desai, Vatsal. “Homology Requirements in Mammalian Early Homologous Recombination .” 2013. Web. 24 Jan 2020.

Vancouver:

Desai V. Homology Requirements in Mammalian Early Homologous Recombination . [Internet] [Thesis]. University of Guelph; 2013. [cited 2020 Jan 24]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6593.

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

Council of Science Editors:

Desai V. Homology Requirements in Mammalian Early Homologous Recombination . [Thesis]. University of Guelph; 2013. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/6593

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


University of South Florida

26. Conine, Grant Mcneil. Topological Data Analysis of Properties of Four-Regular Rigid Vertex Graphs.

Degree: 2014, University of South Florida

Homologous DNA recombination and rearrangement has been modeled with a class of four-regular rigid vertex graphs called assembly graphs which can also be represented by… (more)

Subjects/Keywords: Assembly Graph; Homologous Recombination; Mapper; Topological Data Analysis; Mathematics; Microbiology

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APA (6th Edition):

Conine, G. M. (2014). Topological Data Analysis of Properties of Four-Regular Rigid Vertex Graphs. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5202

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):

Conine, Grant Mcneil. “Topological Data Analysis of Properties of Four-Regular Rigid Vertex Graphs.” 2014. Thesis, University of South Florida. Accessed January 24, 2020. https://scholarcommons.usf.edu/etd/5202.

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

MLA Handbook (7th Edition):

Conine, Grant Mcneil. “Topological Data Analysis of Properties of Four-Regular Rigid Vertex Graphs.” 2014. Web. 24 Jan 2020.

Vancouver:

Conine GM. Topological Data Analysis of Properties of Four-Regular Rigid Vertex Graphs. [Internet] [Thesis]. University of South Florida; 2014. [cited 2020 Jan 24]. Available from: https://scholarcommons.usf.edu/etd/5202.

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

Council of Science Editors:

Conine GM. Topological Data Analysis of Properties of Four-Regular Rigid Vertex Graphs. [Thesis]. University of South Florida; 2014. Available from: https://scholarcommons.usf.edu/etd/5202

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

27. Midgley-Smith, Sarah. DNA replication and replication termination in Escherichia coli.

Degree: PhD, 2019, Brunel University

 A prerequisite for successful cell division is the generation of an accurate copy of the entire genome as well as faithful segregation into the daughter… (more)

Subjects/Keywords: RecG helicase; Chromosome dynamics; 3' exonucleases; homologous recombination; Genomic stability

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APA (6th Edition):

Midgley-Smith, S. (2019). DNA replication and replication termination in Escherichia coli. (Doctoral Dissertation). Brunel University. Retrieved from http://bura.brunel.ac.uk/handle/2438/18142 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774575

Chicago Manual of Style (16th Edition):

Midgley-Smith, Sarah. “DNA replication and replication termination in Escherichia coli.” 2019. Doctoral Dissertation, Brunel University. Accessed January 24, 2020. http://bura.brunel.ac.uk/handle/2438/18142 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774575.

MLA Handbook (7th Edition):

Midgley-Smith, Sarah. “DNA replication and replication termination in Escherichia coli.” 2019. Web. 24 Jan 2020.

Vancouver:

Midgley-Smith S. DNA replication and replication termination in Escherichia coli. [Internet] [Doctoral dissertation]. Brunel University; 2019. [cited 2020 Jan 24]. Available from: http://bura.brunel.ac.uk/handle/2438/18142 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774575.

Council of Science Editors:

Midgley-Smith S. DNA replication and replication termination in Escherichia coli. [Doctoral Dissertation]. Brunel University; 2019. Available from: http://bura.brunel.ac.uk/handle/2438/18142 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774575


Duke University

28. Hum, Yee Fang. Molecular Characterization of Mitotic Homologous Recombination Outcomes in Saccharomyces cerevisiae .

Degree: 2017, Duke University

  Mitotic homologous recombination (HR) is vital for accurate repair of DNA strand breaks caused by endogenous and exogenous sources. However, this high-fidelity repair pathway… (more)

Subjects/Keywords: Genetics; double-strand breaks; genome stability; homologous recombination; yeast

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APA (6th Edition):

Hum, Y. F. (2017). Molecular Characterization of Mitotic Homologous Recombination Outcomes in Saccharomyces cerevisiae . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/16380

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):

Hum, Yee Fang. “Molecular Characterization of Mitotic Homologous Recombination Outcomes in Saccharomyces cerevisiae .” 2017. Thesis, Duke University. Accessed January 24, 2020. http://hdl.handle.net/10161/16380.

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

MLA Handbook (7th Edition):

Hum, Yee Fang. “Molecular Characterization of Mitotic Homologous Recombination Outcomes in Saccharomyces cerevisiae .” 2017. Web. 24 Jan 2020.

Vancouver:

Hum YF. Molecular Characterization of Mitotic Homologous Recombination Outcomes in Saccharomyces cerevisiae . [Internet] [Thesis]. Duke University; 2017. [cited 2020 Jan 24]. Available from: http://hdl.handle.net/10161/16380.

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

Council of Science Editors:

Hum YF. Molecular Characterization of Mitotic Homologous Recombination Outcomes in Saccharomyces cerevisiae . [Thesis]. Duke University; 2017. Available from: http://hdl.handle.net/10161/16380

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


University of Cincinnati

29. Tichy, Elisia D. Double-Strand DNA Break Repair By Homologous Recombination Contributes To The Preservation of Genomic Stability In Mouse Embryonic Stem Cells.

Degree: PhD, Medicine : Cell and Molecular Biology, 2010, University of Cincinnati

 The foundation of proper embryonic development involves the precise control of embryonic stem (ES) cell growth, proliferation, and subsequent differentiation. DNA damage accumulated in the… (more)

Subjects/Keywords: Cellular Biology; Embryonic stem cells; DNA repair; Homologous recombination; Non-homologous end joining; microhomology-mediated end joining

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APA (6th Edition):

Tichy, E. D. (2010). Double-Strand DNA Break Repair By Homologous Recombination Contributes To The Preservation of Genomic Stability In Mouse Embryonic Stem Cells. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1265989840

Chicago Manual of Style (16th Edition):

Tichy, Elisia D. “Double-Strand DNA Break Repair By Homologous Recombination Contributes To The Preservation of Genomic Stability In Mouse Embryonic Stem Cells.” 2010. Doctoral Dissertation, University of Cincinnati. Accessed January 24, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1265989840.

MLA Handbook (7th Edition):

Tichy, Elisia D. “Double-Strand DNA Break Repair By Homologous Recombination Contributes To The Preservation of Genomic Stability In Mouse Embryonic Stem Cells.” 2010. Web. 24 Jan 2020.

Vancouver:

Tichy ED. Double-Strand DNA Break Repair By Homologous Recombination Contributes To The Preservation of Genomic Stability In Mouse Embryonic Stem Cells. [Internet] [Doctoral dissertation]. University of Cincinnati; 2010. [cited 2020 Jan 24]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1265989840.

Council of Science Editors:

Tichy ED. Double-Strand DNA Break Repair By Homologous Recombination Contributes To The Preservation of Genomic Stability In Mouse Embryonic Stem Cells. [Doctoral Dissertation]. University of Cincinnati; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1265989840

30. Tsouroula, Aikaterini. Double strand break repair within constitutive heterochromatin : Étude de la réparation des cassures doubles brins de l'ADN dans l'hétérochromatine constitutive.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2017, Université de Strasbourg

L'hétérochromatine, de nature compacte et répétitive, limite l’accès à l'ADN et fait de la réparation des DSBs un processus difficile que les cellules doivent surmonter… (more)

Subjects/Keywords: Hétérochromatine; CRISPR/ Cas9; NHEJ; HR; RAD51; SSA; Heterochromatin; CRISPR/ Cas9; Non-Homologous End Joining; Homologous recombination; RAD51; Single Strand Annealing; 572.8

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

APA (6th Edition):

Tsouroula, A. (2017). Double strand break repair within constitutive heterochromatin : Étude de la réparation des cassures doubles brins de l'ADN dans l'hétérochromatine constitutive. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAJ036

Chicago Manual of Style (16th Edition):

Tsouroula, Aikaterini. “Double strand break repair within constitutive heterochromatin : Étude de la réparation des cassures doubles brins de l'ADN dans l'hétérochromatine constitutive.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed January 24, 2020. http://www.theses.fr/2017STRAJ036.

MLA Handbook (7th Edition):

Tsouroula, Aikaterini. “Double strand break repair within constitutive heterochromatin : Étude de la réparation des cassures doubles brins de l'ADN dans l'hétérochromatine constitutive.” 2017. Web. 24 Jan 2020.

Vancouver:

Tsouroula A. Double strand break repair within constitutive heterochromatin : Étude de la réparation des cassures doubles brins de l'ADN dans l'hétérochromatine constitutive. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2020 Jan 24]. Available from: http://www.theses.fr/2017STRAJ036.

Council of Science Editors:

Tsouroula A. Double strand break repair within constitutive heterochromatin : Étude de la réparation des cassures doubles brins de l'ADN dans l'hétérochromatine constitutive. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAJ036

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