Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for +publisher:"University of Southern California" +contributor:("Michael, Matthew"). Showing records 1 – 6 of 6 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of Southern California

1. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 17, 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. 17 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 17]. 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

2. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 17, 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. 17 Jun 2019.

Vancouver:

Mastro T. Response to alkylation damage linked to meiotic progression. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2019 Jun 17]. 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

3. Peace, Jared Michael. Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program.

Degree: PhD, Molecular Biology, 2014, University of Southern California

 Eukaryotic cells initiate DNA replication from hundreds to thousands of origins genome wide. The coordinated firing of these origins across a range of times throughout… (more)

Subjects/Keywords: Forkhead; Fkh1; Fkh2; Cdc45; Rif1; Rap1; Pfa4; Mec1; Cdc7; Dbf4; Dbf4 Dependent Kinase (DDK); Orc1; replication origin timing; replication fork rate; chromatin; centromere; telomere; epigenetics; transcription; nuclear architecture; S. cerevisiae

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Peace, J. M. (2014). Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869

Chicago Manual of Style (16th Edition):

Peace, Jared Michael. “Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program.” 2014. Doctoral Dissertation, University of Southern California. Accessed June 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869.

MLA Handbook (7th Edition):

Peace, Jared Michael. “Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program.” 2014. Web. 17 Jun 2019.

Vancouver:

Peace JM. Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Jun 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869.

Council of Science Editors:

Peace JM. Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869


University of Southern California

4. Zhong, Yuan. The role of Cdc7 in replication fork progression in response to DNA damage.

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

 Cdc7-Dbf4 is an essential protein kinase complex required for every single origin firing. As a target of the intra-S checkpoint, Cdc7 kinase activity has also… (more)

Subjects/Keywords: Cdc7; replication fork; DNA damage; fork progression; MMS

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhong, Y. (2012). The role of Cdc7 in replication fork progression in response to DNA damage. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199

Chicago Manual of Style (16th Edition):

Zhong, Yuan. “The role of Cdc7 in replication fork progression in response to DNA damage.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199.

MLA Handbook (7th Edition):

Zhong, Yuan. “The role of Cdc7 in replication fork progression in response to DNA damage.” 2012. Web. 17 Jun 2019.

Vancouver:

Zhong Y. The role of Cdc7 in replication fork progression in response to DNA damage. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jun 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199.

Council of Science Editors:

Zhong Y. The role of Cdc7 in replication fork progression in response to DNA damage. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199


University of Southern California

5. Butuči, Melina. Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells.

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

 During early development in many animals, embryonic cells transition from periods of transcriptional quiescence to abrupt activation of RNA polymerase II (RNAPII)‐dependent transcription on a… (more)

Subjects/Keywords: C. elegans; primordial germ cells; PGC; Z2/Z3; DNA damage; transcription; X chromosome; TOPOII

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Butuči, M. (2015). Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988

Chicago Manual of Style (16th Edition):

Butuči, Melina. “Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells.” 2015. Doctoral Dissertation, University of Southern California. Accessed June 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988.

MLA Handbook (7th Edition):

Butuči, Melina. “Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells.” 2015. Web. 17 Jun 2019.

Vancouver:

Butuči M. Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2019 Jun 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988.

Council of Science Editors:

Butuči M. Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988


University of Southern California

6. Ostrow, Andrew Zachary. Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae.

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

 Forkhead box (FOX) transcription factors regulate a wide variety of cellular functions in higher eukaryotes, including cell cycle control and developmental regulation. In Saccharomyces cerevisiae,… (more)

Subjects/Keywords: replication timing; chromatin; Fkh1; Fkh2; Forkhead; transcription factors; dimer; dimers; dimerization; replication foci; genome architecture; genome structure; chromatin organization; replication origins

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ostrow, A. Z. (2015). Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870

Chicago Manual of Style (16th Edition):

Ostrow, Andrew Zachary. “Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae.” 2015. Doctoral Dissertation, University of Southern California. Accessed June 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870.

MLA Handbook (7th Edition):

Ostrow, Andrew Zachary. “Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae.” 2015. Web. 17 Jun 2019.

Vancouver:

Ostrow AZ. Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2019 Jun 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870.

Council of Science Editors:

Ostrow AZ. Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870

.