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You searched for subject:(1 3 butadiene). Showing records 1 – 5 of 5 total matches.

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University of Minnesota

1. Sangaraju, Dewakar. Mass Spectrometry Based Quantification of 1, 3-Butadiene Induced DNA Adducts: Potential Biomarkers of Cancer Risk.

Degree: PhD, Medicinal Chemistry, 2014, University of Minnesota

 Chemical carcinogenesis involves metabolic activation of carcinogens to electrophilic species which can react with important cellular biomolecules including DNA to form covalent adducts. Covalent carcinogen-DNA… (more)

Subjects/Keywords: 1; 3-Butadiene; Biomarkers; DNA adducts; humans; Mass spectrometry

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

APA (6th Edition):

Sangaraju, D. (2014). Mass Spectrometry Based Quantification of 1, 3-Butadiene Induced DNA Adducts: Potential Biomarkers of Cancer Risk. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/177098

Chicago Manual of Style (16th Edition):

Sangaraju, Dewakar. “Mass Spectrometry Based Quantification of 1, 3-Butadiene Induced DNA Adducts: Potential Biomarkers of Cancer Risk.” 2014. Doctoral Dissertation, University of Minnesota. Accessed September 18, 2019. http://hdl.handle.net/11299/177098.

MLA Handbook (7th Edition):

Sangaraju, Dewakar. “Mass Spectrometry Based Quantification of 1, 3-Butadiene Induced DNA Adducts: Potential Biomarkers of Cancer Risk.” 2014. Web. 18 Sep 2019.

Vancouver:

Sangaraju D. Mass Spectrometry Based Quantification of 1, 3-Butadiene Induced DNA Adducts: Potential Biomarkers of Cancer Risk. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Sep 18]. Available from: http://hdl.handle.net/11299/177098.

Council of Science Editors:

Sangaraju D. Mass Spectrometry Based Quantification of 1, 3-Butadiene Induced DNA Adducts: Potential Biomarkers of Cancer Risk. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/177098


Vanderbilt University

2. Kuo, Dennis W. Structures of the 3,4-Epoxybutene-Derived R- and S-N1-(2-Hydroxy-buten-2-yl) -2' Deoxyinosine DNA Adducts: Regiochemical Control of Glycosidic Torsion Angle Conformation.

Degree: MS, Chemical and Physical Biology, 2015, Vanderbilt University

 Chemical and Physical Biology Structures of the 3,4-Epoxybutene-Derived R- and S-N1-(2-Hydroxy-buten-2-yl) -2' Deoxyinosine DNA Adducts: Regiochemical Control of Glycosidic Torsion Angle Conformation Dennis Kuo Thesis… (more)

Subjects/Keywords: A to G transition; Hoogsteen base pairing; 1; DNA damage; 3-butadiene; inosine adduct; syn conformation

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APA (6th Edition):

Kuo, D. W. (2015). Structures of the 3,4-Epoxybutene-Derived R- and S-N1-(2-Hydroxy-buten-2-yl) -2' Deoxyinosine DNA Adducts: Regiochemical Control of Glycosidic Torsion Angle Conformation. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11232015-140221/ ;

Chicago Manual of Style (16th Edition):

Kuo, Dennis W. “Structures of the 3,4-Epoxybutene-Derived R- and S-N1-(2-Hydroxy-buten-2-yl) -2' Deoxyinosine DNA Adducts: Regiochemical Control of Glycosidic Torsion Angle Conformation.” 2015. Masters Thesis, Vanderbilt University. Accessed September 18, 2019. http://etd.library.vanderbilt.edu/available/etd-11232015-140221/ ;.

MLA Handbook (7th Edition):

Kuo, Dennis W. “Structures of the 3,4-Epoxybutene-Derived R- and S-N1-(2-Hydroxy-buten-2-yl) -2' Deoxyinosine DNA Adducts: Regiochemical Control of Glycosidic Torsion Angle Conformation.” 2015. Web. 18 Sep 2019.

Vancouver:

Kuo DW. Structures of the 3,4-Epoxybutene-Derived R- and S-N1-(2-Hydroxy-buten-2-yl) -2' Deoxyinosine DNA Adducts: Regiochemical Control of Glycosidic Torsion Angle Conformation. [Internet] [Masters thesis]. Vanderbilt University; 2015. [cited 2019 Sep 18]. Available from: http://etd.library.vanderbilt.edu/available/etd-11232015-140221/ ;.

Council of Science Editors:

Kuo DW. Structures of the 3,4-Epoxybutene-Derived R- and S-N1-(2-Hydroxy-buten-2-yl) -2' Deoxyinosine DNA Adducts: Regiochemical Control of Glycosidic Torsion Angle Conformation. [Masters Thesis]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-11232015-140221/ ;


University of Minnesota

3. 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 September 18, 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. 18 Sep 2019.

Vancouver:

Wickramaratne S. Biological Consequences Of Complex Dna Lesions Induced By Bis-Electrophiles. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Sep 18]. 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

4. Magdzinski, Eleanor. The Synthesis, Reactivity and Electrochemical Study of Metallocene Substituted α-Diimine Ligands.

Degree: 2013, University of Western Ontario

 The synthesis of transition metal complexes containing redox-active ligands or ligands with redox-active substituents have been areas of ongoing interest in chemical research. To date,… (more)

Subjects/Keywords: Nitrogen based ligands; redox-active ligands; non-innocent ligands; N-heterocyclic carbenes; main group complexes; diiminopyridine; 1; 4-diaza-1; 3-butadiene; Inorganic Chemistry

…ligands. ............................. 1! Figure 1.2: Processes involving the forming/breaking… …3! Figure 1.3: Redox-active ligands that accept/release electrons. L= non-innocent ligand… …5! Figure 1.5: Diiminopyridine and 1,3-diaza-1,4-butadiene !-diimine ligands… …at 0.5 Vs-1. Experiment carried out inside of an inert atmosphere glove box at room… …DCM / 0.1 M TBAPF6 at 5 Vs-1… 

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APA (6th Edition):

Magdzinski, E. (2013). The Synthesis, Reactivity and Electrochemical Study of Metallocene Substituted α-Diimine Ligands. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1615

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):

Magdzinski, Eleanor. “The Synthesis, Reactivity and Electrochemical Study of Metallocene Substituted α-Diimine Ligands.” 2013. Thesis, University of Western Ontario. Accessed September 18, 2019. https://ir.lib.uwo.ca/etd/1615.

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

MLA Handbook (7th Edition):

Magdzinski, Eleanor. “The Synthesis, Reactivity and Electrochemical Study of Metallocene Substituted α-Diimine Ligands.” 2013. Web. 18 Sep 2019.

Vancouver:

Magdzinski E. The Synthesis, Reactivity and Electrochemical Study of Metallocene Substituted α-Diimine Ligands. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2019 Sep 18]. Available from: https://ir.lib.uwo.ca/etd/1615.

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

Council of Science Editors:

Magdzinski E. The Synthesis, Reactivity and Electrochemical Study of Metallocene Substituted α-Diimine Ligands. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1615

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


Louisiana State University

5. Thomas, Shiju. An Experimental Study on the Formation of Polycyclic Aromatic Hydrocarbons during the Pyrolysis and Oxidation of Catechol[ortho-Dihydroxybenzene]-A Model Compound Representative of Structural Units in Coal, Wood, and Biomass.

Degree: PhD, Chemical Engineering, 2008, Louisiana State University

 Polycyclic aromatic hydrocarbons (PAH) formed during the pyrolysis and combustion of solid fuels like coal, wood, and biomass are widespread environmental pollutants. Since some PAH… (more)

Subjects/Keywords: Effects of temperature; C24H14 PAH; Methylene-bridged PAH; Thermal decomposition products; Polycyclic aromatic hydrocarbons; Effects of oxygen; UV spectra; Acetylene addition.; Catechol pyrolysis; 3-Butadiene addition; 1; High-pressure liquid chromatography

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APA (6th Edition):

Thomas, S. (2008). An Experimental Study on the Formation of Polycyclic Aromatic Hydrocarbons during the Pyrolysis and Oxidation of Catechol[ortho-Dihydroxybenzene]-A Model Compound Representative of Structural Units in Coal, Wood, and Biomass. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-03312008-163317 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2543

Chicago Manual of Style (16th Edition):

Thomas, Shiju. “An Experimental Study on the Formation of Polycyclic Aromatic Hydrocarbons during the Pyrolysis and Oxidation of Catechol[ortho-Dihydroxybenzene]-A Model Compound Representative of Structural Units in Coal, Wood, and Biomass.” 2008. Doctoral Dissertation, Louisiana State University. Accessed September 18, 2019. etd-03312008-163317 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2543.

MLA Handbook (7th Edition):

Thomas, Shiju. “An Experimental Study on the Formation of Polycyclic Aromatic Hydrocarbons during the Pyrolysis and Oxidation of Catechol[ortho-Dihydroxybenzene]-A Model Compound Representative of Structural Units in Coal, Wood, and Biomass.” 2008. Web. 18 Sep 2019.

Vancouver:

Thomas S. An Experimental Study on the Formation of Polycyclic Aromatic Hydrocarbons during the Pyrolysis and Oxidation of Catechol[ortho-Dihydroxybenzene]-A Model Compound Representative of Structural Units in Coal, Wood, and Biomass. [Internet] [Doctoral dissertation]. Louisiana State University; 2008. [cited 2019 Sep 18]. Available from: etd-03312008-163317 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2543.

Council of Science Editors:

Thomas S. An Experimental Study on the Formation of Polycyclic Aromatic Hydrocarbons during the Pyrolysis and Oxidation of Catechol[ortho-Dihydroxybenzene]-A Model Compound Representative of Structural Units in Coal, Wood, and Biomass. [Doctoral Dissertation]. Louisiana State University; 2008. Available from: etd-03312008-163317 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2543

.