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You searched for subject:(Translesion Synthesis). Showing records 1 – 30 of 42 total matches.

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Northeastern University

1. Silva, Michelle Cristine. DNA replication by Escherichia coli DNA polymerase III is regulated by the umuD gene products.

Degree: PhD, Department of Chemistry, 2013, Northeastern University

 DNA polymerase III (DNA pol III) efficiently replicates the Escherichia coli genome, but it cannot bypass DNA damage. Instead, translesion synthesis (TLS) DNA polymerases are… (more)

Subjects/Keywords: DNA damage; DNA replication; Translesion Synthesis; Chemistry

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APA (6th Edition):

Silva, M. C. (2013). DNA replication by Escherichia coli DNA polymerase III is regulated by the umuD gene products. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003301

Chicago Manual of Style (16th Edition):

Silva, Michelle Cristine. “DNA replication by Escherichia coli DNA polymerase III is regulated by the umuD gene products.” 2013. Doctoral Dissertation, Northeastern University. Accessed June 17, 2019. http://hdl.handle.net/2047/d20003301.

MLA Handbook (7th Edition):

Silva, Michelle Cristine. “DNA replication by Escherichia coli DNA polymerase III is regulated by the umuD gene products.” 2013. Web. 17 Jun 2019.

Vancouver:

Silva MC. DNA replication by Escherichia coli DNA polymerase III is regulated by the umuD gene products. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2047/d20003301.

Council of Science Editors:

Silva MC. DNA replication by Escherichia coli DNA polymerase III is regulated by the umuD gene products. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003301

2. Pence, Matthew. Lesion Bypass of N2-ethylguanine by the Human Y Family DNA Polymerases Iota and Kappa.

Degree: 2009, Wake Forest University

 The purpose of this work is to test the hypothesis that the human Y family DNA polymerases have a biological function in the bypass of… (more)

Subjects/Keywords: Translesion Synthesis

…xeroderma pigmentosum-variant T-T dimer thymine-thymine dimer TLS translesion synthesis UBD… …Translesion Synthesis (TLS) DNA polymerases and include DNA polymerases η, ι and κ. The Y… …activation of Translesion Synthesis DNA polymerases at the replication fork for efficient bypass… …increased ability to utilize non-ideal or damaged DNA substrates during synthesis (32;33)… …ethylGua phosphoramidites. Synthesis was carried out using cyanoethyl phosphoramidite chemistry… 

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APA (6th Edition):

Pence, M. (2009). Lesion Bypass of N2-ethylguanine by the Human Y Family DNA Polymerases Iota and Kappa. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/14760

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):

Pence, Matthew. “Lesion Bypass of N2-ethylguanine by the Human Y Family DNA Polymerases Iota and Kappa.” 2009. Thesis, Wake Forest University. Accessed June 17, 2019. http://hdl.handle.net/10339/14760.

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

MLA Handbook (7th Edition):

Pence, Matthew. “Lesion Bypass of N2-ethylguanine by the Human Y Family DNA Polymerases Iota and Kappa.” 2009. Web. 17 Jun 2019.

Vancouver:

Pence M. Lesion Bypass of N2-ethylguanine by the Human Y Family DNA Polymerases Iota and Kappa. [Internet] [Thesis]. Wake Forest University; 2009. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/10339/14760.

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

Council of Science Editors:

Pence M. Lesion Bypass of N2-ethylguanine by the Human Y Family DNA Polymerases Iota and Kappa. [Thesis]. Wake Forest University; 2009. Available from: http://hdl.handle.net/10339/14760

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


University of Iowa

3. Freudenthal, Bret D. Studies of proliferating cell nuclear antigen and its role in translesion synthesis.

Degree: PhD, Biochemistry, 2010, University of Iowa

  One major pathway to overcome DNA damage induced replication blocks is translesion DNA synthesis, which is the replicative bypass of DNA damage by non-classical… (more)

Subjects/Keywords: DNA replication; PCNA; polymerase; translesion synthesis; Biochemistry

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APA (6th Edition):

Freudenthal, B. D. (2010). Studies of proliferating cell nuclear antigen and its role in translesion synthesis. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/668

Chicago Manual of Style (16th Edition):

Freudenthal, Bret D. “Studies of proliferating cell nuclear antigen and its role in translesion synthesis.” 2010. Doctoral Dissertation, University of Iowa. Accessed June 17, 2019. https://ir.uiowa.edu/etd/668.

MLA Handbook (7th Edition):

Freudenthal, Bret D. “Studies of proliferating cell nuclear antigen and its role in translesion synthesis.” 2010. Web. 17 Jun 2019.

Vancouver:

Freudenthal BD. Studies of proliferating cell nuclear antigen and its role in translesion synthesis. [Internet] [Doctoral dissertation]. University of Iowa; 2010. [cited 2019 Jun 17]. Available from: https://ir.uiowa.edu/etd/668.

Council of Science Editors:

Freudenthal BD. Studies of proliferating cell nuclear antigen and its role in translesion synthesis. [Doctoral Dissertation]. University of Iowa; 2010. Available from: https://ir.uiowa.edu/etd/668


Kyoto University / 京都大学

4. Narita, Takeo. Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands : ヒト複製ポリメラーゼδは6-4型光産物の損傷乗越えをする.

Degree: 博士(医学), 2014, Kyoto University / 京都大学

新制・課程博士

甲第18176号

医博第3896号

Subjects/Keywords: DNA Repliation; Translesion Synthesis

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APA (6th Edition):

Narita, T. (2014). Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands : ヒト複製ポリメラーゼδは6-4型光産物の損傷乗越えをする. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/188688 ; http://dx.doi.org/10.14989/doctor.k18176

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):

Narita, Takeo. “Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands : ヒト複製ポリメラーゼδは6-4型光産物の損傷乗越えをする.” 2014. Thesis, Kyoto University / 京都大学. Accessed June 17, 2019. http://hdl.handle.net/2433/188688 ; http://dx.doi.org/10.14989/doctor.k18176.

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

MLA Handbook (7th Edition):

Narita, Takeo. “Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands : ヒト複製ポリメラーゼδは6-4型光産物の損傷乗越えをする.” 2014. Web. 17 Jun 2019.

Vancouver:

Narita T. Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands : ヒト複製ポリメラーゼδは6-4型光産物の損傷乗越えをする. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2433/188688 ; http://dx.doi.org/10.14989/doctor.k18176.

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

Council of Science Editors:

Narita T. Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands : ヒト複製ポリメラーゼδは6-4型光産物の損傷乗越えをする. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/188688 ; http://dx.doi.org/10.14989/doctor.k18176

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


Northeastern University

5. Norton, Matthew. Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli.

Degree: PhD, Department of Biology, 2013, Northeastern University

 Acinetobacter baumannii is a dangerous opportunistic pathogen that has quickly emerged as a source of nosocomial infections for immunocompromised patients. It is able to survive… (more)

Subjects/Keywords: DNA damage; DNA polymerase; pathogen; translesion synthesis; Biology; Molecular Biology

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APA (6th Edition):

Norton, M. (2013). Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003375

Chicago Manual of Style (16th Edition):

Norton, Matthew. “Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli.” 2013. Doctoral Dissertation, Northeastern University. Accessed June 17, 2019. http://hdl.handle.net/2047/d20003375.

MLA Handbook (7th Edition):

Norton, Matthew. “Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli.” 2013. Web. 17 Jun 2019.

Vancouver:

Norton M. Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2047/d20003375.

Council of Science Editors:

Norton M. Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003375


Case Western Reserve University

6. Devadoss, Babho. Probing the Base Stacking Contributions During Translesion DNA Synthesis.

Degree: PhD, Chemistry, 2008, Case Western Reserve University

Translesion DNA synthesis is the ability of a DNA polymerase to misinsert a nucleotide opposite a damaged DNA template. This process can cause mutagenesis resulting… (more)

Subjects/Keywords: Biochemistry; Translesion DNA synthesis; DNA lesions; DNA polymerases

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APA (6th Edition):

Devadoss, B. (2008). Probing the Base Stacking Contributions During Translesion DNA Synthesis. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1222818842

Chicago Manual of Style (16th Edition):

Devadoss, Babho. “Probing the Base Stacking Contributions During Translesion DNA Synthesis.” 2008. Doctoral Dissertation, Case Western Reserve University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1222818842.

MLA Handbook (7th Edition):

Devadoss, Babho. “Probing the Base Stacking Contributions During Translesion DNA Synthesis.” 2008. Web. 17 Jun 2019.

Vancouver:

Devadoss B. Probing the Base Stacking Contributions During Translesion DNA Synthesis. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2008. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1222818842.

Council of Science Editors:

Devadoss B. Probing the Base Stacking Contributions During Translesion DNA Synthesis. [Doctoral Dissertation]. Case Western Reserve University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1222818842


University of California – Riverside

7. Swanson, Ashley Lorraine. Biochemical Characterization of the Replication of Damaged DNA Mediated by Eukaryotic DNA Polymerases.

Degree: Environmental Toxicology, 2014, University of California – Riverside

 DNA lesions can be generated at an estimated rate of up to one million molecular lesions per cell per day, and are induced by a… (more)

Subjects/Keywords: Biochemistry; Chemistry; Toxicology; DNA Damage; DNA Replication; Mutagenesis; Translesion Synthesis

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APA (6th Edition):

Swanson, A. L. (2014). Biochemical Characterization of the Replication of Damaged DNA Mediated by Eukaryotic DNA Polymerases. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/0b73k290

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):

Swanson, Ashley Lorraine. “Biochemical Characterization of the Replication of Damaged DNA Mediated by Eukaryotic DNA Polymerases.” 2014. Thesis, University of California – Riverside. Accessed June 17, 2019. http://www.escholarship.org/uc/item/0b73k290.

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

MLA Handbook (7th Edition):

Swanson, Ashley Lorraine. “Biochemical Characterization of the Replication of Damaged DNA Mediated by Eukaryotic DNA Polymerases.” 2014. Web. 17 Jun 2019.

Vancouver:

Swanson AL. Biochemical Characterization of the Replication of Damaged DNA Mediated by Eukaryotic DNA Polymerases. [Internet] [Thesis]. University of California – Riverside; 2014. [cited 2019 Jun 17]. Available from: http://www.escholarship.org/uc/item/0b73k290.

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

Council of Science Editors:

Swanson AL. Biochemical Characterization of the Replication of Damaged DNA Mediated by Eukaryotic DNA Polymerases. [Thesis]. University of California – Riverside; 2014. Available from: http://www.escholarship.org/uc/item/0b73k290

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

8. Narita, Takeo. Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands .

Degree: 2014, Kyoto University

Subjects/Keywords: DNA Repliation; Translesion Synthesis

Page 1 Page 2

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APA (6th Edition):

Narita, T. (2014). Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/188688

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):

Narita, Takeo. “Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands .” 2014. Thesis, Kyoto University. Accessed June 17, 2019. http://hdl.handle.net/2433/188688.

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

MLA Handbook (7th Edition):

Narita, Takeo. “Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands .” 2014. Web. 17 Jun 2019.

Vancouver:

Narita T. Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands . [Internet] [Thesis]. Kyoto University; 2014. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2433/188688.

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

Council of Science Editors:

Narita T. Human replicative DNA polymerase δ can bypass T-T (6-4) ultraviolet photoproducts on template strands . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/188688

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


Kansas State University

9. Walterhouse, Stephen James. Cervical cancer: An unanticipated consequence of high-risk human papillomavirus infection.

Degree: MS, Division of Biology, 2018, Kansas State University

 Cancer is not a single story, but rather numerous often interwoven tales, each with its own characters and progression. In the case of human papillomavirus… (more)

Subjects/Keywords: Human papilloma virus; Evolution; Translesion synthesis; Protein stability; Cervical cancer

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APA (6th Edition):

Walterhouse, S. J. (2018). Cervical cancer: An unanticipated consequence of high-risk human papillomavirus infection. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/39118

Chicago Manual of Style (16th Edition):

Walterhouse, Stephen James. “Cervical cancer: An unanticipated consequence of high-risk human papillomavirus infection.” 2018. Masters Thesis, Kansas State University. Accessed June 17, 2019. http://hdl.handle.net/2097/39118.

MLA Handbook (7th Edition):

Walterhouse, Stephen James. “Cervical cancer: An unanticipated consequence of high-risk human papillomavirus infection.” 2018. Web. 17 Jun 2019.

Vancouver:

Walterhouse SJ. Cervical cancer: An unanticipated consequence of high-risk human papillomavirus infection. [Internet] [Masters thesis]. Kansas State University; 2018. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2097/39118.

Council of Science Editors:

Walterhouse SJ. Cervical cancer: An unanticipated consequence of high-risk human papillomavirus infection. [Masters Thesis]. Kansas State University; 2018. Available from: http://hdl.handle.net/2097/39118


Vanderbilt University

10. Merkle, Julie Ann. Regulation of Drosophila early embryogenesis and genome maintenance by the E3 ubiquitin ligase no poles.

Degree: PhD, Cell and Developmental Biology, 2011, Vanderbilt University

 In a screen for cell-cycle regulators, we identified a Drosophila maternal effect-lethal mutant that we named âno polesâ (nopo). Embryos from nopo females undergo mitotic… (more)

Subjects/Keywords: translesion synthesis; embryogensis; Drosophila; E3 ubiquitin ligase; genome maintenance

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APA (6th Edition):

Merkle, J. A. (2011). Regulation of Drosophila early embryogenesis and genome maintenance by the E3 ubiquitin ligase no poles. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07212011-151147/ ;

Chicago Manual of Style (16th Edition):

Merkle, Julie Ann. “Regulation of Drosophila early embryogenesis and genome maintenance by the E3 ubiquitin ligase no poles.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed June 17, 2019. http://etd.library.vanderbilt.edu/available/etd-07212011-151147/ ;.

MLA Handbook (7th Edition):

Merkle, Julie Ann. “Regulation of Drosophila early embryogenesis and genome maintenance by the E3 ubiquitin ligase no poles.” 2011. Web. 17 Jun 2019.

Vancouver:

Merkle JA. Regulation of Drosophila early embryogenesis and genome maintenance by the E3 ubiquitin ligase no poles. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Jun 17]. Available from: http://etd.library.vanderbilt.edu/available/etd-07212011-151147/ ;.

Council of Science Editors:

Merkle JA. Regulation of Drosophila early embryogenesis and genome maintenance by the E3 ubiquitin ligase no poles. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-07212011-151147/ ;


Vanderbilt University

11. Politica, Dustin Alan. Structural Consequences of the C8-Guanine DNA Adduct Formed by 3-Nitrobenzanthrone; an Environmental Carcinogen.

Degree: PhD, Chemistry, 2016, Vanderbilt University

 Damage to DNA results from many endogenous and exogenous sources and plays a significant role in cancer etiology. 3-Nitrobenzathrone (3-NBA) is a component of diesel… (more)

Subjects/Keywords: DNA structure; DNA damage; Nitroaromatic; translesion synthesis; damage bypass; Nitroarene

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APA (6th Edition):

Politica, D. A. (2016). Structural Consequences of the C8-Guanine DNA Adduct Formed by 3-Nitrobenzanthrone; an Environmental Carcinogen. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-08012016-091632/ ;

Chicago Manual of Style (16th Edition):

Politica, Dustin Alan. “Structural Consequences of the C8-Guanine DNA Adduct Formed by 3-Nitrobenzanthrone; an Environmental Carcinogen.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed June 17, 2019. http://etd.library.vanderbilt.edu/available/etd-08012016-091632/ ;.

MLA Handbook (7th Edition):

Politica, Dustin Alan. “Structural Consequences of the C8-Guanine DNA Adduct Formed by 3-Nitrobenzanthrone; an Environmental Carcinogen.” 2016. Web. 17 Jun 2019.

Vancouver:

Politica DA. Structural Consequences of the C8-Guanine DNA Adduct Formed by 3-Nitrobenzanthrone; an Environmental Carcinogen. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2019 Jun 17]. Available from: http://etd.library.vanderbilt.edu/available/etd-08012016-091632/ ;.

Council of Science Editors:

Politica DA. Structural Consequences of the C8-Guanine DNA Adduct Formed by 3-Nitrobenzanthrone; an Environmental Carcinogen. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu/available/etd-08012016-091632/ ;


University of Southern California

12. Corzett, Christopher Hale. Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli.

Degree: PhD, Molecular Biology, 2012, University of Southern California

 Escherichia coli DNA polymerases II, IV and V serve dual roles within cells by facilitating efficient replication past potentially lethal DNA damage while simultaneously introducing… (more)

Subjects/Keywords: alternative DNA polymerase; error-prone DNA polymerase; microbial evolution; SOS response; stationary phase; translesion synthesis

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APA (6th Edition):

Corzett, C. H. (2012). Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5053

Chicago Manual of Style (16th Edition):

Corzett, Christopher Hale. “Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5053.

MLA Handbook (7th Edition):

Corzett, Christopher Hale. “Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli.” 2012. Web. 17 Jun 2019.

Vancouver:

Corzett CH. Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jun 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5053.

Council of Science Editors:

Corzett CH. Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5053


University of Southern California

13. Schlacher, Katharina. The mechanism of damage-induced mutations in Escherichia coli.

Degree: PhD, Molecular & Computational Biology, 2006, University of Southern California

 The integrity of the genome is fundamental to the survival of an organism. Escherichia coli possesses an inducible, physiological reaction to DNA damage. The SOS… (more)

Subjects/Keywords: translesion synthesis; pol V; RecA; mutagenesis

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APA (6th Edition):

Schlacher, K. (2006). The mechanism of damage-induced mutations in Escherichia coli. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24711/rec/6971

Chicago Manual of Style (16th Edition):

Schlacher, Katharina. “The mechanism of damage-induced mutations in Escherichia coli.” 2006. Doctoral Dissertation, University of Southern California. Accessed June 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24711/rec/6971.

MLA Handbook (7th Edition):

Schlacher, Katharina. “The mechanism of damage-induced mutations in Escherichia coli.” 2006. Web. 17 Jun 2019.

Vancouver:

Schlacher K. The mechanism of damage-induced mutations in Escherichia coli. [Internet] [Doctoral dissertation]. University of Southern California; 2006. [cited 2019 Jun 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24711/rec/6971.

Council of Science Editors:

Schlacher K. The mechanism of damage-induced mutations in Escherichia coli. [Doctoral Dissertation]. University of Southern California; 2006. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24711/rec/6971


Duke University

14. Wojtaszek, Jessica Louise. Structure and Implication of the Scaffolding Function of Polymerase Rev1 in Translesion Synthesis and Interstrand Crosslink Repair .

Degree: 2015, Duke University

Translesion synthesis is a fundamental biological process that enables DNA replication across lesion sites to ensure timely duplication of genetic information at the cost… (more)

Subjects/Keywords: Biochemistry; Biophysics; Chemistry; FAAP20; interstrand crosslink; Polymerase kappa; Polymerase zeta; Rev1 CTD; translesion synthesis

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APA (6th Edition):

Wojtaszek, J. L. (2015). Structure and Implication of the Scaffolding Function of Polymerase Rev1 in Translesion Synthesis and Interstrand Crosslink Repair . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9936

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):

Wojtaszek, Jessica Louise. “Structure and Implication of the Scaffolding Function of Polymerase Rev1 in Translesion Synthesis and Interstrand Crosslink Repair .” 2015. Thesis, Duke University. Accessed June 17, 2019. http://hdl.handle.net/10161/9936.

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

MLA Handbook (7th Edition):

Wojtaszek, Jessica Louise. “Structure and Implication of the Scaffolding Function of Polymerase Rev1 in Translesion Synthesis and Interstrand Crosslink Repair .” 2015. Web. 17 Jun 2019.

Vancouver:

Wojtaszek JL. Structure and Implication of the Scaffolding Function of Polymerase Rev1 in Translesion Synthesis and Interstrand Crosslink Repair . [Internet] [Thesis]. Duke University; 2015. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/10161/9936.

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

Council of Science Editors:

Wojtaszek JL. Structure and Implication of the Scaffolding Function of Polymerase Rev1 in Translesion Synthesis and Interstrand Crosslink Repair . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/9936

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


Université Montpellier II

15. Tsanov, Nikolay. La voie de dégradation CRL4Cdt2 régule le recrutement des ADN polymérases translésionnelles eta et kappa en foyers nucléaires après endommagements aux UV-C en ciblant pour dégradation les protéines qui contiennent des PIP box spécialisées : The CRL4Cdt2 pathway regulates translesion DNA polymerase eta and kappa focus formation upon UV-C damage by targeting specialized PIP box-containing proteins for degradation.

Degree: Docteur es, Biologie Santé, 2012, Université Montpellier II

La protéine PCNA est un facteur d'échafaudage polyvalent pour plus de cinquante protéines impliquées dans le métabolisme d'ADN, notamment dans la réplication et la réparation.… (more)

Subjects/Keywords: Endommagement de l'ADN; Synthese d'ADN translesionnelle; Degradation proteasomale; DNA damage; Translesion DNA synthesis; Proteasomal degradation

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

APA (6th Edition):

Tsanov, N. (2012). La voie de dégradation CRL4Cdt2 régule le recrutement des ADN polymérases translésionnelles eta et kappa en foyers nucléaires après endommagements aux UV-C en ciblant pour dégradation les protéines qui contiennent des PIP box spécialisées : The CRL4Cdt2 pathway regulates translesion DNA polymerase eta and kappa focus formation upon UV-C damage by targeting specialized PIP box-containing proteins for degradation. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2012MON20213

Chicago Manual of Style (16th Edition):

Tsanov, Nikolay. “La voie de dégradation CRL4Cdt2 régule le recrutement des ADN polymérases translésionnelles eta et kappa en foyers nucléaires après endommagements aux UV-C en ciblant pour dégradation les protéines qui contiennent des PIP box spécialisées : The CRL4Cdt2 pathway regulates translesion DNA polymerase eta and kappa focus formation upon UV-C damage by targeting specialized PIP box-containing proteins for degradation.” 2012. Doctoral Dissertation, Université Montpellier II. Accessed June 17, 2019. http://www.theses.fr/2012MON20213.

MLA Handbook (7th Edition):

Tsanov, Nikolay. “La voie de dégradation CRL4Cdt2 régule le recrutement des ADN polymérases translésionnelles eta et kappa en foyers nucléaires après endommagements aux UV-C en ciblant pour dégradation les protéines qui contiennent des PIP box spécialisées : The CRL4Cdt2 pathway regulates translesion DNA polymerase eta and kappa focus formation upon UV-C damage by targeting specialized PIP box-containing proteins for degradation.” 2012. Web. 17 Jun 2019.

Vancouver:

Tsanov N. La voie de dégradation CRL4Cdt2 régule le recrutement des ADN polymérases translésionnelles eta et kappa en foyers nucléaires après endommagements aux UV-C en ciblant pour dégradation les protéines qui contiennent des PIP box spécialisées : The CRL4Cdt2 pathway regulates translesion DNA polymerase eta and kappa focus formation upon UV-C damage by targeting specialized PIP box-containing proteins for degradation. [Internet] [Doctoral dissertation]. Université Montpellier II; 2012. [cited 2019 Jun 17]. Available from: http://www.theses.fr/2012MON20213.

Council of Science Editors:

Tsanov N. La voie de dégradation CRL4Cdt2 régule le recrutement des ADN polymérases translésionnelles eta et kappa en foyers nucléaires après endommagements aux UV-C en ciblant pour dégradation les protéines qui contiennent des PIP box spécialisées : The CRL4Cdt2 pathway regulates translesion DNA polymerase eta and kappa focus formation upon UV-C damage by targeting specialized PIP box-containing proteins for degradation. [Doctoral Dissertation]. Université Montpellier II; 2012. Available from: http://www.theses.fr/2012MON20213

16. D. Delmastro. EFFECT OF THE LOSS OF RIBONUCLEASE H ACTIVITY ON GENOME INSTABILITY: FROM DNA DAMAGE TOLERANCE TO RETROTRANSPOSITION.

Degree: 2015, Università degli Studi di Milano

 Preserving the entire set of hereditary instructions necessary for life of every organism, genome integrity and identity maintenance is a serious concern for cells. Genomic… (more)

Subjects/Keywords: Ribonuclease H; Translesion Synthesis; ribonucleotides; retrotransposition; Aicardi-Goutières Syndrome; Settore BIO/11 - Biologia Molecolare

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

APA (6th Edition):

Delmastro, D. (2015). EFFECT OF THE LOSS OF RIBONUCLEASE H ACTIVITY ON GENOME INSTABILITY: FROM DNA DAMAGE TOLERANCE TO RETROTRANSPOSITION. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/273893

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):

Delmastro, D.. “EFFECT OF THE LOSS OF RIBONUCLEASE H ACTIVITY ON GENOME INSTABILITY: FROM DNA DAMAGE TOLERANCE TO RETROTRANSPOSITION.” 2015. Thesis, Università degli Studi di Milano. Accessed June 17, 2019. http://hdl.handle.net/2434/273893.

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

MLA Handbook (7th Edition):

Delmastro, D.. “EFFECT OF THE LOSS OF RIBONUCLEASE H ACTIVITY ON GENOME INSTABILITY: FROM DNA DAMAGE TOLERANCE TO RETROTRANSPOSITION.” 2015. Web. 17 Jun 2019.

Vancouver:

Delmastro D. EFFECT OF THE LOSS OF RIBONUCLEASE H ACTIVITY ON GENOME INSTABILITY: FROM DNA DAMAGE TOLERANCE TO RETROTRANSPOSITION. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2434/273893.

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

Council of Science Editors:

Delmastro D. EFFECT OF THE LOSS OF RIBONUCLEASE H ACTIVITY ON GENOME INSTABILITY: FROM DNA DAMAGE TOLERANCE TO RETROTRANSPOSITION. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/273893

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


Ohio University

17. Chen, Yizhang. A Study of Mutagenesis by Translesion Synthesis DNA Polymerases Using A Novel High-throughput Mutation Assay System.

Degree: PhD, Biological Sciences (Arts and Sciences), 2018, Ohio University

 DNA mutations can have devastating effects on cell growth, development, proliferation and survival through the regulation of gene expression and protein activity. Within various processes… (more)

Subjects/Keywords: Biology; DNA Damage; Translesion Synthesis; Mutagenesis; Next-generation Sequencing; Pol Eta; Pol Zeta

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APA (6th Edition):

Chen, Y. (2018). A Study of Mutagenesis by Translesion Synthesis DNA Polymerases Using A Novel High-throughput Mutation Assay System. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1534928845629071

Chicago Manual of Style (16th Edition):

Chen, Yizhang. “A Study of Mutagenesis by Translesion Synthesis DNA Polymerases Using A Novel High-throughput Mutation Assay System.” 2018. Doctoral Dissertation, Ohio University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1534928845629071.

MLA Handbook (7th Edition):

Chen, Yizhang. “A Study of Mutagenesis by Translesion Synthesis DNA Polymerases Using A Novel High-throughput Mutation Assay System.” 2018. Web. 17 Jun 2019.

Vancouver:

Chen Y. A Study of Mutagenesis by Translesion Synthesis DNA Polymerases Using A Novel High-throughput Mutation Assay System. [Internet] [Doctoral dissertation]. Ohio University; 2018. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1534928845629071.

Council of Science Editors:

Chen Y. A Study of Mutagenesis by Translesion Synthesis DNA Polymerases Using A Novel High-throughput Mutation Assay System. [Doctoral Dissertation]. Ohio University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1534928845629071


University of Minnesota

18. Kotapati, Srikanth. Mass spectrometry-based analysis of urinary metabolites of 1,3-Butadiene (BD) in humans and influence of BD-DNA adducts on DNA replication.

Degree: PhD, Medicinal Chemistry, 2013, University of Minnesota

 Cigarette smoking is a known risk factor for the development of lung cancer: approximately 1 out of 5 heavy smokers will develop the disease. However,… (more)

Subjects/Keywords: 1,3-butadiene; Ethnic differences; HPLC; Mass spectrometry; Metabolism; Translesion synthesis; Medicinal chemistry

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

APA (6th Edition):

Kotapati, S. (2013). Mass spectrometry-based analysis of urinary metabolites of 1,3-Butadiene (BD) in humans and influence of BD-DNA adducts on DNA replication. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/168258

Chicago Manual of Style (16th Edition):

Kotapati, Srikanth. “Mass spectrometry-based analysis of urinary metabolites of 1,3-Butadiene (BD) in humans and influence of BD-DNA adducts on DNA replication.” 2013. Doctoral Dissertation, University of Minnesota. Accessed June 17, 2019. http://hdl.handle.net/11299/168258.

MLA Handbook (7th Edition):

Kotapati, Srikanth. “Mass spectrometry-based analysis of urinary metabolites of 1,3-Butadiene (BD) in humans and influence of BD-DNA adducts on DNA replication.” 2013. Web. 17 Jun 2019.

Vancouver:

Kotapati S. Mass spectrometry-based analysis of urinary metabolites of 1,3-Butadiene (BD) in humans and influence of BD-DNA adducts on DNA replication. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11299/168258.

Council of Science Editors:

Kotapati S. Mass spectrometry-based analysis of urinary metabolites of 1,3-Butadiene (BD) in humans and influence of BD-DNA adducts on DNA replication. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://hdl.handle.net/11299/168258


University of Southern California

19. Patel, Meghna. Investigating the E. Coli DNA polymerase V mutasome.

Degree: PhD, Molecular Biology, 2013, University of Southern California

 In Escherichia Coli, cell survival and genomic stability after UV radiation or other DNA damaging agents depends on repair mechanisms induced as part of the… (more)

Subjects/Keywords: translesion DNA synthesis; DNA Polymerase V; error-prone DNA repair; UV mutagenesis

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APA (6th Edition):

Patel, M. (2013). Investigating the E. Coli DNA polymerase V mutasome. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/129615/rec/3623

Chicago Manual of Style (16th Edition):

Patel, Meghna. “Investigating the E. Coli DNA polymerase V mutasome.” 2013. Doctoral Dissertation, University of Southern California. Accessed June 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/129615/rec/3623.

MLA Handbook (7th Edition):

Patel, Meghna. “Investigating the E. Coli DNA polymerase V mutasome.” 2013. Web. 17 Jun 2019.

Vancouver:

Patel M. Investigating the E. Coli DNA polymerase V mutasome. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Jun 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/129615/rec/3623.

Council of Science Editors:

Patel M. Investigating the E. Coli DNA polymerase V mutasome. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/129615/rec/3623


University of Iowa

20. Powers, Kyle Thomas. Structure and function of the disordered regions within translesion synthesis DNA polymerases.

Degree: PhD, Biochemistry, 2018, University of Iowa

  Normal DNA replication is blocked by DNA damage in the template strand. Translesion synthesis is a major pathway for overcoming these replication blocks. In… (more)

Subjects/Keywords: Conformational Dynamics; DNA Damage Bypass; DNA Polymerases; Genome Stability; Intrinsic Disorder; Translesion Synthesis; Biochemistry

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

APA (6th Edition):

Powers, K. T. (2018). Structure and function of the disordered regions within translesion synthesis DNA polymerases. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6625

Chicago Manual of Style (16th Edition):

Powers, Kyle Thomas. “Structure and function of the disordered regions within translesion synthesis DNA polymerases.” 2018. Doctoral Dissertation, University of Iowa. Accessed June 17, 2019. https://ir.uiowa.edu/etd/6625.

MLA Handbook (7th Edition):

Powers, Kyle Thomas. “Structure and function of the disordered regions within translesion synthesis DNA polymerases.” 2018. Web. 17 Jun 2019.

Vancouver:

Powers KT. Structure and function of the disordered regions within translesion synthesis DNA polymerases. [Internet] [Doctoral dissertation]. University of Iowa; 2018. [cited 2019 Jun 17]. Available from: https://ir.uiowa.edu/etd/6625.

Council of Science Editors:

Powers KT. Structure and function of the disordered regions within translesion synthesis DNA polymerases. [Doctoral Dissertation]. University of Iowa; 2018. Available from: https://ir.uiowa.edu/etd/6625


National University of Ireland – Galway

21. Conmy, Sarah Angela. Characterisation of UVA-induced DNA damage responses in human skin cells .

Degree: 2013, National University of Ireland – Galway

 Accumulating evidence indicates that exposure to long-wavelength ultraviolet A (UVA) radiation (315-400 nm), which accounts for >95% of solar UV radiation reaching the earth's surface,… (more)

Subjects/Keywords: UVA-radiation; Melanoma; Melanocytes; DNA polymerase eta; Translesion synthesis; Department of Biochemistry; School of Natural Science

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APA (6th Edition):

Conmy, S. A. (2013). Characterisation of UVA-induced DNA damage responses in human skin cells . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/4410

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):

Conmy, Sarah Angela. “Characterisation of UVA-induced DNA damage responses in human skin cells .” 2013. Thesis, National University of Ireland – Galway. Accessed June 17, 2019. http://hdl.handle.net/10379/4410.

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

MLA Handbook (7th Edition):

Conmy, Sarah Angela. “Characterisation of UVA-induced DNA damage responses in human skin cells .” 2013. Web. 17 Jun 2019.

Vancouver:

Conmy SA. Characterisation of UVA-induced DNA damage responses in human skin cells . [Internet] [Thesis]. National University of Ireland – Galway; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/10379/4410.

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

Council of Science Editors:

Conmy SA. Characterisation of UVA-induced DNA damage responses in human skin cells . [Thesis]. National University of Ireland – Galway; 2013. Available from: http://hdl.handle.net/10379/4410

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


Northeastern University

22. Cafarelli, Tiziana Moccia. Features of the Escherichia coli DinB multi-protein complex and the mechanisms by which it regulates DinB's structure and fidelity.

Degree: PhD, Department of Biology, 2013, Northeastern University

 DNA Polymerase IV, or DinB, of Escherichia coli is the most evolutionarily conserved and abundant translesion DNA polymerase. This error-prone DNA polymerase is regulated not… (more)

Subjects/Keywords: DinB; DNA polymerase; multi-protein complex; RecA; Translesion synthesis; Biochemistry; Biochemistry, Biophysics, and Structural Biology; Biology; Molecular Biology

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APA (6th Edition):

Cafarelli, T. M. (2013). Features of the Escherichia coli DinB multi-protein complex and the mechanisms by which it regulates DinB's structure and fidelity. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20004848

Chicago Manual of Style (16th Edition):

Cafarelli, Tiziana Moccia. “Features of the Escherichia coli DinB multi-protein complex and the mechanisms by which it regulates DinB's structure and fidelity.” 2013. Doctoral Dissertation, Northeastern University. Accessed June 17, 2019. http://hdl.handle.net/2047/d20004848.

MLA Handbook (7th Edition):

Cafarelli, Tiziana Moccia. “Features of the Escherichia coli DinB multi-protein complex and the mechanisms by which it regulates DinB's structure and fidelity.” 2013. Web. 17 Jun 2019.

Vancouver:

Cafarelli TM. Features of the Escherichia coli DinB multi-protein complex and the mechanisms by which it regulates DinB's structure and fidelity. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2047/d20004848.

Council of Science Editors:

Cafarelli TM. Features of the Escherichia coli DinB multi-protein complex and the mechanisms by which it regulates DinB's structure and fidelity. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20004848

23. Tsuda, Masataka. In vivo evidence for translesion synthesis by the replicative DNA polymerase δ .

Degree: 2017, Kyoto University

Subjects/Keywords: translesion synthesis; replicative polymerase; UV lesions; proofreading; piggyBlock assay

Page 1 Page 2

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APA (6th Edition):

Tsuda, M. (2017). In vivo evidence for translesion synthesis by the replicative DNA polymerase δ . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/225985

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):

Tsuda, Masataka. “In vivo evidence for translesion synthesis by the replicative DNA polymerase δ .” 2017. Thesis, Kyoto University. Accessed June 17, 2019. http://hdl.handle.net/2433/225985.

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

MLA Handbook (7th Edition):

Tsuda, Masataka. “In vivo evidence for translesion synthesis by the replicative DNA polymerase δ .” 2017. Web. 17 Jun 2019.

Vancouver:

Tsuda M. In vivo evidence for translesion synthesis by the replicative DNA polymerase δ . [Internet] [Thesis]. Kyoto University; 2017. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2433/225985.

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

Council of Science Editors:

Tsuda M. In vivo evidence for translesion synthesis by the replicative DNA polymerase δ . [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/225985

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


Kyoto University / 京都大学

24. Tsuda, Masataka. In vivo evidence for translesion synthesis by the replicative DNA polymerase δ : 複製DNAポリメラーゼδによる損傷乗越え合成のin vivoでの証拠.

Degree: 博士(医学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20559号

医博第4244号

Subjects/Keywords: translesion synthesis; replicative polymerase; UV lesions; proofreading; piggyBlock assay

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APA (6th Edition):

Tsuda, M. (2017). In vivo evidence for translesion synthesis by the replicative DNA polymerase δ : 複製DNAポリメラーゼδによる損傷乗越え合成のin vivoでの証拠. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/225985 ; http://dx.doi.org/10.14989/doctor.k20559

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):

Tsuda, Masataka. “In vivo evidence for translesion synthesis by the replicative DNA polymerase δ : 複製DNAポリメラーゼδによる損傷乗越え合成のin vivoでの証拠.” 2017. Thesis, Kyoto University / 京都大学. Accessed June 17, 2019. http://hdl.handle.net/2433/225985 ; http://dx.doi.org/10.14989/doctor.k20559.

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

MLA Handbook (7th Edition):

Tsuda, Masataka. “In vivo evidence for translesion synthesis by the replicative DNA polymerase δ : 複製DNAポリメラーゼδによる損傷乗越え合成のin vivoでの証拠.” 2017. Web. 17 Jun 2019.

Vancouver:

Tsuda M. In vivo evidence for translesion synthesis by the replicative DNA polymerase δ : 複製DNAポリメラーゼδによる損傷乗越え合成のin vivoでの証拠. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/2433/225985 ; http://dx.doi.org/10.14989/doctor.k20559.

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

Council of Science Editors:

Tsuda M. In vivo evidence for translesion synthesis by the replicative DNA polymerase δ : 複製DNAポリメラーゼδによる損傷乗越え合成のin vivoでの証拠. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/225985 ; http://dx.doi.org/10.14989/doctor.k20559

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


The Ohio State University

25. Tokarsky, E. John Paul. Analysis of Human Y-Family DNA Polymerases and PrimPol by Pre-Steady-State Kinetic Methods.

Degree: PhD, Biophysics, 2018, The Ohio State University

 Eukaryotic genomic DNA is efficiently and accurately replicated to ensure that an exact copy is created before cell division occurs. The complex machinery involved in… (more)

Subjects/Keywords: Biochemistry; Biology; Biophysics; DNA polymerase; PrimPol; Pre-steady-state kinetics; translesion dna synthesis; Y-family DNA polymerase; DNA replication; biochemistry

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APA (6th Edition):

Tokarsky, E. J. P. (2018). Analysis of Human Y-Family DNA Polymerases and PrimPol by Pre-Steady-State Kinetic Methods. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1533913136156371

Chicago Manual of Style (16th Edition):

Tokarsky, E John Paul. “Analysis of Human Y-Family DNA Polymerases and PrimPol by Pre-Steady-State Kinetic Methods.” 2018. Doctoral Dissertation, The Ohio State University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1533913136156371.

MLA Handbook (7th Edition):

Tokarsky, E John Paul. “Analysis of Human Y-Family DNA Polymerases and PrimPol by Pre-Steady-State Kinetic Methods.” 2018. Web. 17 Jun 2019.

Vancouver:

Tokarsky EJP. Analysis of Human Y-Family DNA Polymerases and PrimPol by Pre-Steady-State Kinetic Methods. [Internet] [Doctoral dissertation]. The Ohio State University; 2018. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1533913136156371.

Council of Science Editors:

Tokarsky EJP. Analysis of Human Y-Family DNA Polymerases and PrimPol by Pre-Steady-State Kinetic Methods. [Doctoral Dissertation]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1533913136156371


University of Minnesota

26. Wickramaratne, Susith. Biological Consequences Of Complex Dna Lesions Induced By Bis-Electrophiles.

Degree: PhD, Chemistry, 2014, University of Minnesota

 Genomic DNA is constantly modified by bis–electrophiles which induce a wide array of DNA adducts. DNA adducts can threaten cell viability and genomic integrity by… (more)

Subjects/Keywords: 1; 3-butadiene; base excision repair; DNA adducts; DNA-protein cross-links; replication bypass; translesion synthesis

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APA (6th Edition):

Wickramaratne, S. (2014). Biological Consequences Of Complex Dna Lesions Induced By Bis-Electrophiles. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174906

Chicago Manual of Style (16th Edition):

Wickramaratne, Susith. “Biological Consequences Of Complex Dna Lesions Induced By Bis-Electrophiles.” 2014. Doctoral Dissertation, University of Minnesota. Accessed June 17, 2019. http://hdl.handle.net/11299/174906.

MLA Handbook (7th Edition):

Wickramaratne, Susith. “Biological Consequences Of Complex Dna Lesions Induced By Bis-Electrophiles.” 2014. Web. 17 Jun 2019.

Vancouver:

Wickramaratne S. Biological Consequences Of Complex Dna Lesions Induced By Bis-Electrophiles. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11299/174906.

Council of Science Editors:

Wickramaratne S. Biological Consequences Of Complex Dna Lesions Induced By Bis-Electrophiles. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/174906


Vanderbilt University

27. Millsap, Amy Danae. Translesion Synthesis of N2 and C8-Deoxyguanosine Adducts of the Dietary Mutagen 2-Amino-3-methylimidazo-[4,5-f]-quinoline (IQ): Participation in Observed Mutagenic Spectra.

Degree: PhD, Chemistry, 2015, Vanderbilt University

 2-Amino-3-methylimidizo-[4,5-ʄ]-quinoline (IQ), a potent dietary mutagen, forms DNA adducts at the N&178; and C8-positions of 2ʹ-deoxyguanosine. IQ induces G to A transitions and G to… (more)

Subjects/Keywords: DNA Adducts; Translesion Synthesis; 2-Amino-3-methylimidazo-[4; 5-f]-quinoline; Heterocyclic Amines; DNA Polymerases

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APA (6th Edition):

Millsap, A. D. (2015). Translesion Synthesis of N2 and C8-Deoxyguanosine Adducts of the Dietary Mutagen 2-Amino-3-methylimidazo-[4,5-f]-quinoline (IQ): Participation in Observed Mutagenic Spectra. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11192015-095602/ ;

Chicago Manual of Style (16th Edition):

Millsap, Amy Danae. “Translesion Synthesis of N2 and C8-Deoxyguanosine Adducts of the Dietary Mutagen 2-Amino-3-methylimidazo-[4,5-f]-quinoline (IQ): Participation in Observed Mutagenic Spectra.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed June 17, 2019. http://etd.library.vanderbilt.edu/available/etd-11192015-095602/ ;.

MLA Handbook (7th Edition):

Millsap, Amy Danae. “Translesion Synthesis of N2 and C8-Deoxyguanosine Adducts of the Dietary Mutagen 2-Amino-3-methylimidazo-[4,5-f]-quinoline (IQ): Participation in Observed Mutagenic Spectra.” 2015. Web. 17 Jun 2019.

Vancouver:

Millsap AD. Translesion Synthesis of N2 and C8-Deoxyguanosine Adducts of the Dietary Mutagen 2-Amino-3-methylimidazo-[4,5-f]-quinoline (IQ): Participation in Observed Mutagenic Spectra. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Jun 17]. Available from: http://etd.library.vanderbilt.edu/available/etd-11192015-095602/ ;.

Council of Science Editors:

Millsap AD. Translesion Synthesis of N2 and C8-Deoxyguanosine Adducts of the Dietary Mutagen 2-Amino-3-methylimidazo-[4,5-f]-quinoline (IQ): Participation in Observed Mutagenic Spectra. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-11192015-095602/ ;

28. Sokol, Anna Magdalena. Roles of DNA polymerase eta and replication protein A (RPA) in undamaged and platinum-treated human cells .

Degree: 2012, National University of Ireland – Galway

 Platinum-based drugs are widely used in cancer therapy. Bypass of platinum-induced DNA adducts during DNA replication by specialised DNA polymerases may contribute to drug tolerance… (more)

Subjects/Keywords: Platinum chemotherapeutics; DNA damage response; Translesion synthesis; Biochemistry Department

…repair, translesion synthesis, replication protein A (RPA) Chapter 1 1.1 The cell… …progression past UV-induced DNA lesions mediated by translesion synthesis (TLS) (… …replicatively, for example by translesion synthesis (Branzei and Foiani, 2010; Lehmann and Fuchs… …Hoeijmakers, 2009). 1.3.2.1 Translesion synthesis (TLS) and DNA polymerase η (… …process of translesion synthesis (TLS) plays an important role in preventing… 

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APA (6th Edition):

Sokol, A. M. (2012). Roles of DNA polymerase eta and replication protein A (RPA) in undamaged and platinum-treated human cells . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/3394

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):

Sokol, Anna Magdalena. “Roles of DNA polymerase eta and replication protein A (RPA) in undamaged and platinum-treated human cells .” 2012. Thesis, National University of Ireland – Galway. Accessed June 17, 2019. http://hdl.handle.net/10379/3394.

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

MLA Handbook (7th Edition):

Sokol, Anna Magdalena. “Roles of DNA polymerase eta and replication protein A (RPA) in undamaged and platinum-treated human cells .” 2012. Web. 17 Jun 2019.

Vancouver:

Sokol AM. Roles of DNA polymerase eta and replication protein A (RPA) in undamaged and platinum-treated human cells . [Internet] [Thesis]. National University of Ireland – Galway; 2012. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/10379/3394.

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

Council of Science Editors:

Sokol AM. Roles of DNA polymerase eta and replication protein A (RPA) in undamaged and platinum-treated human cells . [Thesis]. National University of Ireland – Galway; 2012. Available from: http://hdl.handle.net/10379/3394

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


Case Western Reserve University

29. Motea, Edward A. Probing the Chemistry and Enzymology of Translesion DNA Synthesis: Applications in Developing a Novel “Theranostic” Agent against Leukemia.

Degree: PhD, Chemistry, 2012, Case Western Reserve University

 The replication and maintenance of the genetic information stored in DNA are required for all forms of life. As such, any inappropriate alteration to the… (more)

Subjects/Keywords: Biochemistry; Biomedical Research; Chemistry; Molecular Biology; Molecular Chemistry; Organic Chemistry; Pharmacology; translesion DNA synthesis; DNA polymerase; non-natural nucleotides; enzymology; DNA replication; abasic site; acute lymphoblastic leukemia; bioconjugation; chemical biology

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

APA (6th Edition):

Motea, E. A. (2012). Probing the Chemistry and Enzymology of Translesion DNA Synthesis: Applications in Developing a Novel “Theranostic” Agent against Leukemia. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1323382718

Chicago Manual of Style (16th Edition):

Motea, Edward A. “Probing the Chemistry and Enzymology of Translesion DNA Synthesis: Applications in Developing a Novel “Theranostic” Agent against Leukemia.” 2012. Doctoral Dissertation, Case Western Reserve University. Accessed June 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1323382718.

MLA Handbook (7th Edition):

Motea, Edward A. “Probing the Chemistry and Enzymology of Translesion DNA Synthesis: Applications in Developing a Novel “Theranostic” Agent against Leukemia.” 2012. Web. 17 Jun 2019.

Vancouver:

Motea EA. Probing the Chemistry and Enzymology of Translesion DNA Synthesis: Applications in Developing a Novel “Theranostic” Agent against Leukemia. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2012. [cited 2019 Jun 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1323382718.

Council of Science Editors:

Motea EA. Probing the Chemistry and Enzymology of Translesion DNA Synthesis: Applications in Developing a Novel “Theranostic” Agent against Leukemia. [Doctoral Dissertation]. Case Western Reserve University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1323382718


University of Central Florida

30. Hall, Ashley. Assessment And In Vitro Repair Of Damaged Dna Templates From Forensic Stains.

Degree: 2005, University of Central Florida

 DNA extracted from biological stains is often intractable to analysis. This may due to a number of factors including a low copy number (LCN) of… (more)

Subjects/Keywords: in vitro DNA repair; translesion synthesis; base excision repair; DNA damage; forensic; Chemistry

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

APA (6th Edition):

Hall, A. (2005). Assessment And In Vitro Repair Of Damaged Dna Templates From Forensic Stains. (Doctoral Dissertation). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/562

Chicago Manual of Style (16th Edition):

Hall, Ashley. “Assessment And In Vitro Repair Of Damaged Dna Templates From Forensic Stains.” 2005. Doctoral Dissertation, University of Central Florida. Accessed June 17, 2019. https://stars.library.ucf.edu/etd/562.

MLA Handbook (7th Edition):

Hall, Ashley. “Assessment And In Vitro Repair Of Damaged Dna Templates From Forensic Stains.” 2005. Web. 17 Jun 2019.

Vancouver:

Hall A. Assessment And In Vitro Repair Of Damaged Dna Templates From Forensic Stains. [Internet] [Doctoral dissertation]. University of Central Florida; 2005. [cited 2019 Jun 17]. Available from: https://stars.library.ucf.edu/etd/562.

Council of Science Editors:

Hall A. Assessment And In Vitro Repair Of Damaged Dna Templates From Forensic Stains. [Doctoral Dissertation]. University of Central Florida; 2005. Available from: https://stars.library.ucf.edu/etd/562

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