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You searched for subject:(alkylation damage). Showing records 1 – 6 of 6 total matches.

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University of Lethbridge

1. University of Lethbridge. Faculty of Arts and Science. Computational investigations of alkylation damage to the DNA nucleobase thymine .

Degree: 2019, University of Lethbridge

 DNA alkylation damage is caused by numerous sources in the environment. Alkylation damage can stall standard DNA polymerases and replication instead occurs through a process… (more)

Subjects/Keywords: alkylation; computational chemistry; DNA damage; human TLS polymerase eta; thymine; thymine alkylation damage; Dissertations, Academic

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

APA (6th Edition):

Science, U. o. L. F. o. A. a. (2019). Computational investigations of alkylation damage to the DNA nucleobase thymine . (Thesis). University of Lethbridge. Retrieved from http://hdl.handle.net/10133/5564

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):

Science, University of Lethbridge. Faculty of Arts and. “Computational investigations of alkylation damage to the DNA nucleobase thymine .” 2019. Thesis, University of Lethbridge. Accessed January 26, 2020. http://hdl.handle.net/10133/5564.

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

MLA Handbook (7th Edition):

Science, University of Lethbridge. Faculty of Arts and. “Computational investigations of alkylation damage to the DNA nucleobase thymine .” 2019. Web. 26 Jan 2020.

Vancouver:

Science UoLFoAa. Computational investigations of alkylation damage to the DNA nucleobase thymine . [Internet] [Thesis]. University of Lethbridge; 2019. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/10133/5564.

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

Council of Science Editors:

Science UoLFoAa. Computational investigations of alkylation damage to the DNA nucleobase thymine . [Thesis]. University of Lethbridge; 2019. Available from: http://hdl.handle.net/10133/5564

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


Boston University

2. Ahmad, Alya. Human targeted deletions and biological roles of genes involved in repair of alkylation damage.

Degree: MS, Medical Sciences, 2015, Boston University

 DNA repair is not a single mechanism found within cells. There exists numerous different DNA repair mechanisms that function within every type of cell. The… (more)

Subjects/Keywords: Cellular biology; ALKBH; Alkylation damage; Direct reversal repair; DNA repair

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APA (6th Edition):

Ahmad, A. (2015). Human targeted deletions and biological roles of genes involved in repair of alkylation damage. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/16247

Chicago Manual of Style (16th Edition):

Ahmad, Alya. “Human targeted deletions and biological roles of genes involved in repair of alkylation damage.” 2015. Masters Thesis, Boston University. Accessed January 26, 2020. http://hdl.handle.net/2144/16247.

MLA Handbook (7th Edition):

Ahmad, Alya. “Human targeted deletions and biological roles of genes involved in repair of alkylation damage.” 2015. Web. 26 Jan 2020.

Vancouver:

Ahmad A. Human targeted deletions and biological roles of genes involved in repair of alkylation damage. [Internet] [Masters thesis]. Boston University; 2015. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/2144/16247.

Council of Science Editors:

Ahmad A. Human targeted deletions and biological roles of genes involved in repair of alkylation damage. [Masters Thesis]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16247


University of Southern California

3. Le, Anh-Huy Phan. The importance of Dfp1 in alkylation damage response and meiosis.

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

 In Schizosaccharomyces pombe, the DDK complex is a conserved, essential kinase complex consisting of a catalytic subunit, Hsk1 (Cdc7), and its regulatory subunit Dfp1 (Dbf4).… (more)

Subjects/Keywords: alkylation damage; DDK; Dfp1; Hsk1; meiosis; S. Pombe

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APA (6th Edition):

Le, A. P. (2011). The importance of Dfp1 in alkylation damage response and meiosis. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856

Chicago Manual of Style (16th Edition):

Le, Anh-Huy Phan. “The importance of Dfp1 in alkylation damage response and meiosis.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 26, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856.

MLA Handbook (7th Edition):

Le, Anh-Huy Phan. “The importance of Dfp1 in alkylation damage response and meiosis.” 2011. Web. 26 Jan 2020.

Vancouver:

Le AP. The importance of Dfp1 in alkylation damage response and meiosis. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jan 26]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856.

Council of Science Editors:

Le AP. The importance of Dfp1 in alkylation damage response and meiosis. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856


University of California – Riverside

4. Williams, Nicole Lynn. Replicative and Transcriptional Bypass of Alkylated and Alpha-Anomeric Lesions.

Degree: Environmental Toxicology, 2017, University of California – Riverside

 Exposure to a variety of endogenous and exogenous sources of DNA damaging agents can lead to the formation of 104-106 DNA lesions per cell per… (more)

Subjects/Keywords: Molecular biology; Alkylation; DNA Damage; DNA Repair; Replication; Transcription

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APA (6th Edition):

Williams, N. L. (2017). Replicative and Transcriptional Bypass of Alkylated and Alpha-Anomeric Lesions. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/3rv8b678

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):

Williams, Nicole Lynn. “Replicative and Transcriptional Bypass of Alkylated and Alpha-Anomeric Lesions.” 2017. Thesis, University of California – Riverside. Accessed January 26, 2020. http://www.escholarship.org/uc/item/3rv8b678.

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

MLA Handbook (7th Edition):

Williams, Nicole Lynn. “Replicative and Transcriptional Bypass of Alkylated and Alpha-Anomeric Lesions.” 2017. Web. 26 Jan 2020.

Vancouver:

Williams NL. Replicative and Transcriptional Bypass of Alkylated and Alpha-Anomeric Lesions. [Internet] [Thesis]. University of California – Riverside; 2017. [cited 2020 Jan 26]. Available from: http://www.escholarship.org/uc/item/3rv8b678.

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

Council of Science Editors:

Williams NL. Replicative and Transcriptional Bypass of Alkylated and Alpha-Anomeric Lesions. [Thesis]. University of California – Riverside; 2017. Available from: http://www.escholarship.org/uc/item/3rv8b678

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


University of Toledo Health Science Campus

5. Kaliyaperumal, Saravanan. hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?.

Degree: PhD, College of Medicine, 2009, University of Toledo Health Science Campus

 The Mismatch repair (MMR) system maintains genomic stability byrepairing DNA mismatches and insertion-deletion loops (IDLs) resulting from replicationand recombination errors. Defective MMR can lead to… (more)

Subjects/Keywords: Biology; DNA Repair; Protein Phosphorylation; mismatch repair; alkylation damage response; MSH6 Protein Phosphorylation; MNNG damage signaling

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APA (6th Edition):

Kaliyaperumal, S. (2009). hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021

Chicago Manual of Style (16th Edition):

Kaliyaperumal, Saravanan. “hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?.” 2009. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed January 26, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021.

MLA Handbook (7th Edition):

Kaliyaperumal, Saravanan. “hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?.” 2009. Web. 26 Jan 2020.

Vancouver:

Kaliyaperumal S. hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2009. [cited 2020 Jan 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021.

Council of Science Editors:

Kaliyaperumal S. hMSH6 Protein Phosphorylation: DNA Mismatch Repair or DNA Damage Signaling?. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1242933021


Northeastern University

6. Muenter, Mark Manfred. E. coli cellular tolerance to alkylating agents chloroacetaldehyde, styrene oxide, and benzyl bromide.

Degree: PhD, Department of Chemistry and Chemical Biology, 2016, Northeastern University

 Alkylating agents are used in cancer chemotherapy as cytotoxic agents, in manufacturing, and can form as byproducts of industrial processes such as drug synthetic pathways.… (more)

Subjects/Keywords: benzyl bromide; chloroacetaldehyde; DNA; E. coli; styrene oxide; Alkylating agents; Alkylation; DNA damage; DNA adducts; Escherichia coli; Organic compounds

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

APA (6th Edition):

Muenter, M. M. (2016). E. coli cellular tolerance to alkylating agents chloroacetaldehyde, styrene oxide, and benzyl bromide. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20214607

Chicago Manual of Style (16th Edition):

Muenter, Mark Manfred. “E. coli cellular tolerance to alkylating agents chloroacetaldehyde, styrene oxide, and benzyl bromide.” 2016. Doctoral Dissertation, Northeastern University. Accessed January 26, 2020. http://hdl.handle.net/2047/D20214607.

MLA Handbook (7th Edition):

Muenter, Mark Manfred. “E. coli cellular tolerance to alkylating agents chloroacetaldehyde, styrene oxide, and benzyl bromide.” 2016. Web. 26 Jan 2020.

Vancouver:

Muenter MM. E. coli cellular tolerance to alkylating agents chloroacetaldehyde, styrene oxide, and benzyl bromide. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2020 Jan 26]. Available from: http://hdl.handle.net/2047/D20214607.

Council of Science Editors:

Muenter MM. E. coli cellular tolerance to alkylating agents chloroacetaldehyde, styrene oxide, and benzyl bromide. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20214607

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