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You searched for +publisher:"University of Southern California" +contributor:("Goodman, Myron F."). Showing records 1 – 16 of 16 total matches.

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University of Southern California

1. Jiang, Qingfei. Activation mechanism of damaged-induced DNA polymerase V in Escherichia coli.

Degree: PhD, Chemistry, 2009, University of Southern California

 In Escherichia coli, cell survival and genomic stability after UV radiation depends on DNA repair mechanisms induced in response to DNA damage as part of… (more)

Subjects/Keywords: DNA damage

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APA (6th Edition):

Jiang, Q. (2009). Activation mechanism of damaged-induced DNA polymerase V in Escherichia coli. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/272072/rec/496

Chicago Manual of Style (16th Edition):

Jiang, Qingfei. “Activation mechanism of damaged-induced DNA polymerase V in Escherichia coli.” 2009. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/272072/rec/496.

MLA Handbook (7th Edition):

Jiang, Qingfei. “Activation mechanism of damaged-induced DNA polymerase V in Escherichia coli.” 2009. Web. 24 Jun 2019.

Vancouver:

Jiang Q. Activation mechanism of damaged-induced DNA polymerase V in Escherichia coli. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/272072/rec/496.

Council of Science Editors:

Jiang Q. Activation mechanism of damaged-induced DNA polymerase V in Escherichia coli. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/272072/rec/496


University of Southern California

2. Erdem, Ayşen Lisa. The role of ATP in the regulation of Escherichia coli DNA polymerase V activity.

Degree: PhD, Molecular Biology, 2015, University of Southern California

 In Escherichia coli, DNA damage elicits the well regulated SOS response, which occurs in two phases. The first phase of SOS is dominated by accurate… (more)

Subjects/Keywords: pol V; pol V Mut; RecA; ATP; ATP hydrolysis; regulation; Rum; R391

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APA (6th Edition):

Erdem, A. L. (2015). The role of ATP in the regulation of Escherichia coli DNA polymerase V activity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/538236/rec/7191

Chicago Manual of Style (16th Edition):

Erdem, Ayşen Lisa. “The role of ATP in the regulation of Escherichia coli DNA polymerase V activity.” 2015. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/538236/rec/7191.

MLA Handbook (7th Edition):

Erdem, Ayşen Lisa. “The role of ATP in the regulation of Escherichia coli DNA polymerase V activity.” 2015. Web. 24 Jun 2019.

Vancouver:

Erdem AL. The role of ATP in the regulation of Escherichia coli DNA polymerase V activity. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/538236/rec/7191.

Council of Science Editors:

Erdem AL. The role of ATP in the regulation of Escherichia coli DNA polymerase V activity. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/538236/rec/7191


University of Southern California

3. Chamberlain, Brian Thomas. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.

Degree: PhD, Chemistry, 2012, University of Southern California

 A variety of triphosphate analogs that replace a natural phosphate anhydride P-O-P linkage with a phosphonate P-CXY-P moiety have been synthesized for the characterization of… (more)

Subjects/Keywords: bisphosphonates; organoazides; nucleotides; polymerase

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APA (6th Edition):

Chamberlain, B. T. (2012). Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837

Chicago Manual of Style (16th Edition):

Chamberlain, Brian Thomas. “Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837.

MLA Handbook (7th Edition):

Chamberlain, Brian Thomas. “Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.” 2012. Web. 24 Jun 2019.

Vancouver:

Chamberlain BT. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837.

Council of Science Editors:

Chamberlain BT. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837


University of Southern California

4. Upton, Thomas George. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.

Degree: PhD, Chemistry, 2009, University of Southern California

 A stereoelectronically varied series of alpha-substituted methylenebisphosphonic acids (X,Y = H, F, Cl, Br, CH3) was synthesized and used to prepare corresponding dNTP beta,y-CXY and… (more)

Subjects/Keywords: DNA polymerase beta; bisphosphonates; titrations; fluorination; trifluoromethylation; halogenation; nucleotide analogues; stereoselectivity; autodock; docking; inhibitor design; HIV reverse transcriptase; polymerase kinetics

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APA (6th Edition):

Upton, T. G. (2009). Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859

Chicago Manual of Style (16th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859.

MLA Handbook (7th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Web. 24 Jun 2019.

Vancouver:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859.

Council of Science Editors:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859


University of Southern California

5. Oertell, Keriann Michelle. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.

Degree: PhD, Chemistry, 2013, University of Southern California

 A β,γ-bridging oxygen substituted dNTP toolkit comprising a variety of steric and electrostatic properties has been synthesized and used to investigate DNA polymerase β. Surprisingly,… (more)

Subjects/Keywords: kinetics; fidelity; polymerase

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APA (6th Edition):

Oertell, K. M. (2013). DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071

Chicago Manual of Style (16th Edition):

Oertell, Keriann Michelle. “DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.” 2013. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071.

MLA Handbook (7th Edition):

Oertell, Keriann Michelle. “DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.” 2013. Web. 24 Jun 2019.

Vancouver:

Oertell KM. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071.

Council of Science Editors:

Oertell KM. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071


University of Southern California

6. 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 24, 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. 24 Jun 2019.

Vancouver:

Patel M. Investigating the E. Coli DNA polymerase V mutasome. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Jun 24]. 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 Southern California

7. Mu, Yunxiang. DNA deamination and binding properties of wild type and HIGM2 mutants of activation induced cytidine daminase.

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

 AID is required for SHM and CSR as an initiator protein. Hyper IgM syndrome 2, a primary immunological deficiency disorder caused by AICDA gene (encoding… (more)

Subjects/Keywords: deaminase; apobec; hyper IgM syndrome; class switch recombination; somatic hypermutation

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APA (6th Edition):

Mu, Y. (2012). DNA deamination and binding properties of wild type and HIGM2 mutants of activation induced cytidine daminase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/1674/rec/2062

Chicago Manual of Style (16th Edition):

Mu, Yunxiang. “DNA deamination and binding properties of wild type and HIGM2 mutants of activation induced cytidine daminase.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/1674/rec/2062.

MLA Handbook (7th Edition):

Mu, Yunxiang. “DNA deamination and binding properties of wild type and HIGM2 mutants of activation induced cytidine daminase.” 2012. Web. 24 Jun 2019.

Vancouver:

Mu Y. DNA deamination and binding properties of wild type and HIGM2 mutants of activation induced cytidine daminase. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/1674/rec/2062.

Council of Science Editors:

Mu Y. DNA deamination and binding properties of wild type and HIGM2 mutants of activation induced cytidine daminase. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/1674/rec/2062


University of Southern California

8. Chang, Yu-Hao Paul. Structural studies of two key factors for DNA replication in eukaryotic cells.

Degree: PhD, Genetic, Molecular & Cellular Biology, 2012, University of Southern California

 Genomic DNA replication is essential for the transmission of genetic information; during this process, minichromosome maintenance (MCM) complex, the cellular replicative helicase, unwinds duplex DNA… (more)

Subjects/Keywords: DNA replication; GINS origin; helicase; SV40 large T antigen

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APA (6th Edition):

Chang, Y. P. (2012). Structural studies of two key factors for DNA replication in eukaryotic cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/366483/rec/6119

Chicago Manual of Style (16th Edition):

Chang, Yu-Hao Paul. “Structural studies of two key factors for DNA replication in eukaryotic cells.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/366483/rec/6119.

MLA Handbook (7th Edition):

Chang, Yu-Hao Paul. “Structural studies of two key factors for DNA replication in eukaryotic cells.” 2012. Web. 24 Jun 2019.

Vancouver:

Chang YP. Structural studies of two key factors for DNA replication in eukaryotic cells. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/366483/rec/6119.

Council of Science Editors:

Chang YP. Structural studies of two key factors for DNA replication in eukaryotic cells. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/366483/rec/6119


University of Southern California

9. Mastro, Tara. Response to alkylation damage linked to meiotic progression.

Degree: PhD, Molecular Biology, 2015, University of Southern California

 Mechanisms that maintain genome stability are essential for human health. Loss of genome stability is associated with cancer and birth defects. This dissertation uses a… (more)

Subjects/Keywords: meiosis; S. pombe; DNA damage; checkpoint; chromosomes; genetics

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APA (6th Edition):

Mastro, T. (2015). Response to alkylation damage linked to meiotic progression. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/535465/rec/5564

Chicago Manual of Style (16th Edition):

Mastro, Tara. “Response to alkylation damage linked to meiotic progression.” 2015. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/535465/rec/5564.

MLA Handbook (7th Edition):

Mastro, Tara. “Response to alkylation damage linked to meiotic progression.” 2015. Web. 24 Jun 2019.

Vancouver:

Mastro T. Response to alkylation damage linked to meiotic progression. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/535465/rec/5564.

Council of Science Editors:

Mastro T. Response to alkylation damage linked to meiotic progression. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/535465/rec/5564


University of Southern California

10. Watanabe, Go. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2017, University of Southern California

 Nonhomologous DNA end joining (NHEJ) is the major repair mechanism for double‐strand DNA breaks. One of the key components in human NHEJ is DNA‐dependent protein… (more)

Subjects/Keywords: DNA repair; NHEJ; DNA-PKcs; X-ray crystallography

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APA (6th Edition):

Watanabe, G. (2017). X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971

Chicago Manual of Style (16th Edition):

Watanabe, Go. “X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.” 2017. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971.

MLA Handbook (7th Edition):

Watanabe, Go. “X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.” 2017. Web. 24 Jun 2019.

Vancouver:

Watanabe G. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971.

Council of Science Editors:

Watanabe G. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971


University of Southern California

11. 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 24, 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. 24 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 24]. 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

12. Holden, Lauren Georgianna. A structure based study of the HIV restriction factor APOBEC3G.

Degree: PhD, Molecular Biology, 2011, University of Southern California

 The Apolipoprotein B editing enzyme catalytic polypeptide-like (APOBEC) family of 11 proteins deaminate cytidines on either single-stranded DNA (ssDNA) or RNA substrates, introducing C to… (more)

Subjects/Keywords: cytidine deaminase; X-ray crystallography; anti-HIV

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APA (6th Edition):

Holden, L. G. (2011). A structure based study of the HIV restriction factor APOBEC3G. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376

Chicago Manual of Style (16th Edition):

Holden, Lauren Georgianna. “A structure based study of the HIV restriction factor APOBEC3G.” 2011. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376.

MLA Handbook (7th Edition):

Holden, Lauren Georgianna. “A structure based study of the HIV restriction factor APOBEC3G.” 2011. Web. 24 Jun 2019.

Vancouver:

Holden LG. A structure based study of the HIV restriction factor APOBEC3G. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376.

Council of Science Editors:

Holden LG. A structure based study of the HIV restriction factor APOBEC3G. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376


University of Southern California

13. Wu, Yue. Novel stereochemical probes for DNA polymerases: nucleoside triphosphate beta,gamma-CXY analogues.

Degree: PhD, Chemistry, 2013, University of Southern California

 2’-Deoxynucleoside 5’-triphosphate analogues with β,γ-bridging oxygen replaced by a CXY group are useful chemical probes to investigate DNA polymerase catalytic and base‐selection mechanisms. A long‐standing… (more)

Subjects/Keywords: analogue; bisphosphonate; chiral; diastereomer; nucleotide; polymerase

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APA (6th Edition):

Wu, Y. (2013). Novel stereochemical probes for DNA polymerases: nucleoside triphosphate beta,gamma-CXY analogues. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/359801/rec/4468

Chicago Manual of Style (16th Edition):

Wu, Yue. “Novel stereochemical probes for DNA polymerases: nucleoside triphosphate beta,gamma-CXY analogues.” 2013. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/359801/rec/4468.

MLA Handbook (7th Edition):

Wu, Yue. “Novel stereochemical probes for DNA polymerases: nucleoside triphosphate beta,gamma-CXY analogues.” 2013. Web. 24 Jun 2019.

Vancouver:

Wu Y. Novel stereochemical probes for DNA polymerases: nucleoside triphosphate beta,gamma-CXY analogues. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/359801/rec/4468.

Council of Science Editors:

Wu Y. Novel stereochemical probes for DNA polymerases: nucleoside triphosphate beta,gamma-CXY analogues. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/359801/rec/4468


University of Southern California

14. 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 24, 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. 24 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 24]. 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


University of Southern California

15. Prochnow, Courtney. The crystal structure of APOBEC-2 and implications for APOBEC enzymes.

Degree: PhD, Molecular Biology, 2008, University of Southern California

 APOBEC-2 (Apo2) belongs to the Apolioprotein B (APOB) mRNA-editing enzyme catalytic polypeptide (APOBEC) family of cytidine deaminases that modify genes by deaminating cytosines in mRNA… (more)

Subjects/Keywords: APOBEC; cytidine deaminase; HIV; cytidine deamination; activation induced cytidine deaminase; AID; APOBEC-2

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

APA (6th Edition):

Prochnow, C. (2008). The crystal structure of APOBEC-2 and implications for APOBEC enzymes. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531

Chicago Manual of Style (16th Edition):

Prochnow, Courtney. “The crystal structure of APOBEC-2 and implications for APOBEC enzymes.” 2008. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531.

MLA Handbook (7th Edition):

Prochnow, Courtney. “The crystal structure of APOBEC-2 and implications for APOBEC enzymes.” 2008. Web. 24 Jun 2019.

Vancouver:

Prochnow C. The crystal structure of APOBEC-2 and implications for APOBEC enzymes. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531.

Council of Science Editors:

Prochnow C. The crystal structure of APOBEC-2 and implications for APOBEC enzymes. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531


University of Southern California

16. Sucato, Christopher Anthony. The contribution of chemical steps to DNA polymerase beta catalysis and fidelity.

Degree: PhD, Chemistry, 2008, University of Southern California

 The mechanism of DNA polymerase beta-catalyzed nucleotidyl transfer consists of chemical steps involving primer 3 OH deprotonation, nucleophilic attack, and pyrophosphate leaving-group elimination, preceded by… (more)

Subjects/Keywords: DNA polymerase; mechanistic enzymology; enzyme kinetics; base excision repair; replication fidelity; dNTP analogs

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

APA (6th Edition):

Sucato, C. A. (2008). The contribution of chemical steps to DNA polymerase beta catalysis and fidelity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/40504/rec/6522

Chicago Manual of Style (16th Edition):

Sucato, Christopher Anthony. “The contribution of chemical steps to DNA polymerase beta catalysis and fidelity.” 2008. Doctoral Dissertation, University of Southern California. Accessed June 24, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/40504/rec/6522.

MLA Handbook (7th Edition):

Sucato, Christopher Anthony. “The contribution of chemical steps to DNA polymerase beta catalysis and fidelity.” 2008. Web. 24 Jun 2019.

Vancouver:

Sucato CA. The contribution of chemical steps to DNA polymerase beta catalysis and fidelity. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2019 Jun 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/40504/rec/6522.

Council of Science Editors:

Sucato CA. The contribution of chemical steps to DNA polymerase beta catalysis and fidelity. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/40504/rec/6522

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