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You searched for subject:(OXYGEN BIOCHEMISTRY ). Showing records 1 – 30 of 94 total matches.

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University of California – Berkeley

1. RoseFigura, Jordan M. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.

Degree: Chemistry, 2010, University of California – Berkeley

 PQQ is an exogenous, tricyclic, quino-cofactor for a number of bacterial dehydrogenase reaction. It has also been proposed to play a role as a bacterial… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; Oxygen activation; PQQ

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

APA (6th Edition):

RoseFigura, J. M. (2010). Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4jh004zw

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):

RoseFigura, Jordan M. “Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.” 2010. Thesis, University of California – Berkeley. Accessed June 06, 2020. http://www.escholarship.org/uc/item/4jh004zw.

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

MLA Handbook (7th Edition):

RoseFigura, Jordan M. “Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms.” 2010. Web. 06 Jun 2020.

Vancouver:

RoseFigura JM. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/4jh004zw.

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

Council of Science Editors:

RoseFigura JM. Investigation of the structure and mechanism of a PQQ biosynthetic pathway component, PqqC, and a bioinformatics analysis of potential PQQ producing organisms. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/4jh004zw

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


University of California – Berkeley

2. Collazo, Lara Patricia. Investigating Gas Migration in Enzymes: Dioxygen Channels inside of Soybean Lipoxygenase 1.

Degree: Molecular & Cell Biology, 2013, University of California – Berkeley

 Enzymes are complex systems that contain a variety of pockets, clefts, and channels throughout the protein matrix. These gaps and tunnels represent potential transport pathways… (more)

Subjects/Keywords: Molecular biology; Biochemistry; catalysis; channels; lipoxygenase; migration; oxygen; regiospecificity

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APA (6th Edition):

Collazo, L. P. (2013). Investigating Gas Migration in Enzymes: Dioxygen Channels inside of Soybean Lipoxygenase 1. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/7rj361gs

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):

Collazo, Lara Patricia. “Investigating Gas Migration in Enzymes: Dioxygen Channels inside of Soybean Lipoxygenase 1.” 2013. Thesis, University of California – Berkeley. Accessed June 06, 2020. http://www.escholarship.org/uc/item/7rj361gs.

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

MLA Handbook (7th Edition):

Collazo, Lara Patricia. “Investigating Gas Migration in Enzymes: Dioxygen Channels inside of Soybean Lipoxygenase 1.” 2013. Web. 06 Jun 2020.

Vancouver:

Collazo LP. Investigating Gas Migration in Enzymes: Dioxygen Channels inside of Soybean Lipoxygenase 1. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/7rj361gs.

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

Council of Science Editors:

Collazo LP. Investigating Gas Migration in Enzymes: Dioxygen Channels inside of Soybean Lipoxygenase 1. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/7rj361gs

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


University of California – San Diego

3. Babakhanlou, Madlina. Candidate Gene Identified in Humans Adapted to High-Altitude Depicts Hypoxia Tolerance in Drosophila melanogaster.

Degree: Biology, 2018, University of California – San Diego

 High altitude studies have been insightful in revealing putative hypoxia tolerant genes to improve pathological and physiological conditions that involve hypoxia or ischemia. Whole-genome sequencing… (more)

Subjects/Keywords: Biology; Biochemistry; Genetics; high altitude; HSL; hypoxia; lipase; lipolysis; oxygen

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APA (6th Edition):

Babakhanlou, M. (2018). Candidate Gene Identified in Humans Adapted to High-Altitude Depicts Hypoxia Tolerance in Drosophila melanogaster. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/6064x7qq

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):

Babakhanlou, Madlina. “Candidate Gene Identified in Humans Adapted to High-Altitude Depicts Hypoxia Tolerance in Drosophila melanogaster.” 2018. Thesis, University of California – San Diego. Accessed June 06, 2020. http://www.escholarship.org/uc/item/6064x7qq.

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

MLA Handbook (7th Edition):

Babakhanlou, Madlina. “Candidate Gene Identified in Humans Adapted to High-Altitude Depicts Hypoxia Tolerance in Drosophila melanogaster.” 2018. Web. 06 Jun 2020.

Vancouver:

Babakhanlou M. Candidate Gene Identified in Humans Adapted to High-Altitude Depicts Hypoxia Tolerance in Drosophila melanogaster. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/6064x7qq.

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

Council of Science Editors:

Babakhanlou M. Candidate Gene Identified in Humans Adapted to High-Altitude Depicts Hypoxia Tolerance in Drosophila melanogaster. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/6064x7qq

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


Temple University

4. Deliu, Elena. GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation.

Degree: PhD, 2012, Temple University

Pharmacology

The G protein-coupled estrogen receptor GPER/GPER1, also known as GPR30, was originally cloned as an orphan receptor and later shown to be specifically activated… (more)

Subjects/Keywords: Pharmacology; Biochemistry; calcium imaging; estrogen; gpr30; pain; reactive oxygen species

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APA (6th Edition):

Deliu, E. (2012). GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,194862

Chicago Manual of Style (16th Edition):

Deliu, Elena. “GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation.” 2012. Doctoral Dissertation, Temple University. Accessed June 06, 2020. http://digital.library.temple.edu/u?/p245801coll10,194862.

MLA Handbook (7th Edition):

Deliu, Elena. “GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation.” 2012. Web. 06 Jun 2020.

Vancouver:

Deliu E. GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation. [Internet] [Doctoral dissertation]. Temple University; 2012. [cited 2020 Jun 06]. Available from: http://digital.library.temple.edu/u?/p245801coll10,194862.

Council of Science Editors:

Deliu E. GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation. [Doctoral Dissertation]. Temple University; 2012. Available from: http://digital.library.temple.edu/u?/p245801coll10,194862


University of Pennsylvania

5. Sheehan, Molly Marie. Engineering Oxygen Reactivity in Heme-Protein Maquettes.

Degree: 2014, University of Pennsylvania

 Fundamental questions of protein cofactor oxygen reactivity are left unanswered even after years of research due to the limitations imposed by the complexity of natural… (more)

Subjects/Keywords: design; globin; minimal; oxygen; protein; ROS; Biochemistry; Biophysics

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APA (6th Edition):

Sheehan, M. M. (2014). Engineering Oxygen Reactivity in Heme-Protein Maquettes. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1438

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):

Sheehan, Molly Marie. “Engineering Oxygen Reactivity in Heme-Protein Maquettes.” 2014. Thesis, University of Pennsylvania. Accessed June 06, 2020. https://repository.upenn.edu/edissertations/1438.

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

MLA Handbook (7th Edition):

Sheehan, Molly Marie. “Engineering Oxygen Reactivity in Heme-Protein Maquettes.” 2014. Web. 06 Jun 2020.

Vancouver:

Sheehan MM. Engineering Oxygen Reactivity in Heme-Protein Maquettes. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2020 Jun 06]. Available from: https://repository.upenn.edu/edissertations/1438.

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

Council of Science Editors:

Sheehan MM. Engineering Oxygen Reactivity in Heme-Protein Maquettes. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1438

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


The Ohio State University

6. Zhao, Ran. A study of photodynamic damage to the DNA replication system.

Degree: PhD, Ohio State Biochemistry Program, 2009, The Ohio State University

  Photodynamic therapy (PDT) is a promising clinical modality for killing unwanted cells,especially cancer cells by the combined use of light, photosensitizers and molecular oxygen.In… (more)

Subjects/Keywords: Biochemistry; Photodynamic Damage; Singlet Oxygen; DNA Replication; Ruthenium Complexes; Topoisomerase Poison

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APA (6th Edition):

Zhao, R. (2009). A study of photodynamic damage to the DNA replication system. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1259685879

Chicago Manual of Style (16th Edition):

Zhao, Ran. “A study of photodynamic damage to the DNA replication system.” 2009. Doctoral Dissertation, The Ohio State University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1259685879.

MLA Handbook (7th Edition):

Zhao, Ran. “A study of photodynamic damage to the DNA replication system.” 2009. Web. 06 Jun 2020.

Vancouver:

Zhao R. A study of photodynamic damage to the DNA replication system. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259685879.

Council of Science Editors:

Zhao R. A study of photodynamic damage to the DNA replication system. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1259685879


The Ohio State University

7. Zhang, Ning. Design of high molecular weight polymerized hemoglobins for use in transfusion medicine and monocyte/macrophage hemoglobin-based drug delivery systems.

Degree: PhD, Biochemistry Program, Ohio State, 2011, The Ohio State University

 Hemoglobin (Hb) is a unique protein with both the ability to transport oxygen and to target monocytes and macrophages. Therefore, Hb could be used in… (more)

Subjects/Keywords: Biochemistry; Hemoglobin; Hb; oxygen delivery; drug delivery; polymerized Hb

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APA (6th Edition):

Zhang, N. (2011). Design of high molecular weight polymerized hemoglobins for use in transfusion medicine and monocyte/macrophage hemoglobin-based drug delivery systems. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1318952866

Chicago Manual of Style (16th Edition):

Zhang, Ning. “Design of high molecular weight polymerized hemoglobins for use in transfusion medicine and monocyte/macrophage hemoglobin-based drug delivery systems.” 2011. Doctoral Dissertation, The Ohio State University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1318952866.

MLA Handbook (7th Edition):

Zhang, Ning. “Design of high molecular weight polymerized hemoglobins for use in transfusion medicine and monocyte/macrophage hemoglobin-based drug delivery systems.” 2011. Web. 06 Jun 2020.

Vancouver:

Zhang N. Design of high molecular weight polymerized hemoglobins for use in transfusion medicine and monocyte/macrophage hemoglobin-based drug delivery systems. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1318952866.

Council of Science Editors:

Zhang N. Design of high molecular weight polymerized hemoglobins for use in transfusion medicine and monocyte/macrophage hemoglobin-based drug delivery systems. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1318952866


University of North Carolina – Greensboro

8. Beravolu, Shilpa. Calcium and chloride as cofactors and their binding in photosystem II.

Degree: 2018, University of North Carolina – Greensboro

 Photosystem II (PSII) is the membrane-bound protein complex which participates in the photosynthetic conversion of sunlight energy into chemical energy and produces molecular oxygen. Calcium… (more)

Subjects/Keywords: Photosynthetic oxygen evolution; Binding sites (Biochemistry); Chlorides; Calcium

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APA (6th Edition):

Beravolu, S. (2018). Calcium and chloride as cofactors and their binding in photosystem II. (Masters Thesis). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=23122

Chicago Manual of Style (16th Edition):

Beravolu, Shilpa. “Calcium and chloride as cofactors and their binding in photosystem II.” 2018. Masters Thesis, University of North Carolina – Greensboro. Accessed June 06, 2020. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=23122.

MLA Handbook (7th Edition):

Beravolu, Shilpa. “Calcium and chloride as cofactors and their binding in photosystem II.” 2018. Web. 06 Jun 2020.

Vancouver:

Beravolu S. Calcium and chloride as cofactors and their binding in photosystem II. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2018. [cited 2020 Jun 06]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=23122.

Council of Science Editors:

Beravolu S. Calcium and chloride as cofactors and their binding in photosystem II. [Masters Thesis]. University of North Carolina – Greensboro; 2018. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=23122


University of Pennsylvania

9. Auman, Dirk. Uncovering Biophysical Determinants Of Oxidoreductase Function Through De Novo Protein Design.

Degree: 2019, University of Pennsylvania

 Oxidoreductases are a diverse class of enzymes defined by their chemical role of transferring electrons from one substrate to another. Comprising the functional cores of… (more)

Subjects/Keywords: flavin; heme; magnetic sensing; oxygen; protein engineering; transport; Biochemistry; Biophysics

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APA (6th Edition):

Auman, D. (2019). Uncovering Biophysical Determinants Of Oxidoreductase Function Through De Novo Protein Design. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3521

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):

Auman, Dirk. “Uncovering Biophysical Determinants Of Oxidoreductase Function Through De Novo Protein Design.” 2019. Thesis, University of Pennsylvania. Accessed June 06, 2020. https://repository.upenn.edu/edissertations/3521.

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

MLA Handbook (7th Edition):

Auman, Dirk. “Uncovering Biophysical Determinants Of Oxidoreductase Function Through De Novo Protein Design.” 2019. Web. 06 Jun 2020.

Vancouver:

Auman D. Uncovering Biophysical Determinants Of Oxidoreductase Function Through De Novo Protein Design. [Internet] [Thesis]. University of Pennsylvania; 2019. [cited 2020 Jun 06]. Available from: https://repository.upenn.edu/edissertations/3521.

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

Council of Science Editors:

Auman D. Uncovering Biophysical Determinants Of Oxidoreductase Function Through De Novo Protein Design. [Thesis]. University of Pennsylvania; 2019. Available from: https://repository.upenn.edu/edissertations/3521

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


Rice University

10. Salter, Mallory D. Ligand Diffusion Pathways and Mechanisms for Regulating Oxygen Affinity in Two Model Invertebrate Globins: The E7 Gate and Apolar Tunnel.

Degree: PhD, Natural Sciences, 2011, Rice University

 The major pathway for O 2 binding to mammalian myoglobins (Mbs) and hemoglobins (Hbs) involves transient outward movements of the distal histidine (HisE7), which allows… (more)

Subjects/Keywords: Pure sciences; Hemoglobin; Ligand diffusion; Oxygen binding; Biochemistry

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APA (6th Edition):

Salter, M. D. (2011). Ligand Diffusion Pathways and Mechanisms for Regulating Oxygen Affinity in Two Model Invertebrate Globins: The E7 Gate and Apolar Tunnel. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/70423

Chicago Manual of Style (16th Edition):

Salter, Mallory D. “Ligand Diffusion Pathways and Mechanisms for Regulating Oxygen Affinity in Two Model Invertebrate Globins: The E7 Gate and Apolar Tunnel.” 2011. Doctoral Dissertation, Rice University. Accessed June 06, 2020. http://hdl.handle.net/1911/70423.

MLA Handbook (7th Edition):

Salter, Mallory D. “Ligand Diffusion Pathways and Mechanisms for Regulating Oxygen Affinity in Two Model Invertebrate Globins: The E7 Gate and Apolar Tunnel.” 2011. Web. 06 Jun 2020.

Vancouver:

Salter MD. Ligand Diffusion Pathways and Mechanisms for Regulating Oxygen Affinity in Two Model Invertebrate Globins: The E7 Gate and Apolar Tunnel. [Internet] [Doctoral dissertation]. Rice University; 2011. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1911/70423.

Council of Science Editors:

Salter MD. Ligand Diffusion Pathways and Mechanisms for Regulating Oxygen Affinity in Two Model Invertebrate Globins: The E7 Gate and Apolar Tunnel. [Doctoral Dissertation]. Rice University; 2011. Available from: http://hdl.handle.net/1911/70423

11. Beravolu, Shilpa. Calcium and chloride as cofactors and their binding in photosystem II.

Degree: 2018, NC Docks

 Photosystem II (PSII) is the membrane-bound protein complex which participates in the photosynthetic conversion of sunlight energy into chemical energy and produces molecular oxygen. Calcium… (more)

Subjects/Keywords: Photosynthetic oxygen evolution; Binding sites (Biochemistry); Chlorides; Calcium

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APA (6th Edition):

Beravolu, S. (2018). Calcium and chloride as cofactors and their binding in photosystem II. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/uncg/f/Beravolu_uncg_0154M_12354.pdf

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):

Beravolu, Shilpa. “Calcium and chloride as cofactors and their binding in photosystem II.” 2018. Thesis, NC Docks. Accessed June 06, 2020. http://libres.uncg.edu/ir/uncg/f/Beravolu_uncg_0154M_12354.pdf.

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

MLA Handbook (7th Edition):

Beravolu, Shilpa. “Calcium and chloride as cofactors and their binding in photosystem II.” 2018. Web. 06 Jun 2020.

Vancouver:

Beravolu S. Calcium and chloride as cofactors and their binding in photosystem II. [Internet] [Thesis]. NC Docks; 2018. [cited 2020 Jun 06]. Available from: http://libres.uncg.edu/ir/uncg/f/Beravolu_uncg_0154M_12354.pdf.

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

Council of Science Editors:

Beravolu S. Calcium and chloride as cofactors and their binding in photosystem II. [Thesis]. NC Docks; 2018. Available from: http://libres.uncg.edu/ir/uncg/f/Beravolu_uncg_0154M_12354.pdf

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


University of Oxford

12. Wulff, Philip. Principles of hydrogen catalysis in the presence of oxygen by a [NiFe] hydrogenase from E. coli.

Degree: PhD, 2014, University of Oxford

 [NiFe] hydrogenases are metalloenzymes that act as highly efficient molecular electrocatalysts for the interconversion of protons and molecular hydrogen. Unlike any other known molecular electrocatalyst,… (more)

Subjects/Keywords: 541; Biochemistry; Chemistry & allied sciences; Physical Sciences; Electrochemistry and electrolysis; Enzymes; Biosensors; oxidase; hydrogen; nickel-iron hydrogenase; oxygen tolerance; mass spectrometry; reactive oxygen species; oxygen isotopes

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APA (6th Edition):

Wulff, P. (2014). Principles of hydrogen catalysis in the presence of oxygen by a [NiFe] hydrogenase from E. coli. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:9e434467-d50b-484a-a17e-ef3091636269 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640081

Chicago Manual of Style (16th Edition):

Wulff, Philip. “Principles of hydrogen catalysis in the presence of oxygen by a [NiFe] hydrogenase from E. coli.” 2014. Doctoral Dissertation, University of Oxford. Accessed June 06, 2020. http://ora.ox.ac.uk/objects/uuid:9e434467-d50b-484a-a17e-ef3091636269 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640081.

MLA Handbook (7th Edition):

Wulff, Philip. “Principles of hydrogen catalysis in the presence of oxygen by a [NiFe] hydrogenase from E. coli.” 2014. Web. 06 Jun 2020.

Vancouver:

Wulff P. Principles of hydrogen catalysis in the presence of oxygen by a [NiFe] hydrogenase from E. coli. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jun 06]. Available from: http://ora.ox.ac.uk/objects/uuid:9e434467-d50b-484a-a17e-ef3091636269 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640081.

Council of Science Editors:

Wulff P. Principles of hydrogen catalysis in the presence of oxygen by a [NiFe] hydrogenase from E. coli. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:9e434467-d50b-484a-a17e-ef3091636269 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.640081


Case Western Reserve University

13. Ye, Fang. PPAR¿ and Smad2 Mediate Ski Induced Energy Metabolism Shift and Oncogenic Transformation.

Degree: PhD, Biochemistry, 2010, Case Western Reserve University

  Ski is a versatile nuclear oncoprotein that regulates transcriptions of genes involved in multiple biological processes. Ski induces oncogenic transformation of chicken embryo fibroblasts… (more)

Subjects/Keywords: Biochemistry; Ski, TGF-&946; , Smad2, Smad3, PPAR&947; , &946; -oxidation, transformation, metabolism, mitochondria, oxygen consumption

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APA (6th Edition):

Ye, F. (2010). PPAR¿ and Smad2 Mediate Ski Induced Energy Metabolism Shift and Oncogenic Transformation. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1280930750

Chicago Manual of Style (16th Edition):

Ye, Fang. “PPAR¿ and Smad2 Mediate Ski Induced Energy Metabolism Shift and Oncogenic Transformation.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1280930750.

MLA Handbook (7th Edition):

Ye, Fang. “PPAR¿ and Smad2 Mediate Ski Induced Energy Metabolism Shift and Oncogenic Transformation.” 2010. Web. 06 Jun 2020.

Vancouver:

Ye F. PPAR¿ and Smad2 Mediate Ski Induced Energy Metabolism Shift and Oncogenic Transformation. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1280930750.

Council of Science Editors:

Ye F. PPAR¿ and Smad2 Mediate Ski Induced Energy Metabolism Shift and Oncogenic Transformation. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1280930750


University of California – Berkeley

14. Dickinson, Bryan Craig. Molecular Imaging Approaches to Understanding the Roles of Hydrogen Peroxide Biology in Stress and Development.

Degree: Chemistry, 2010, University of California – Berkeley

 The production of hydrogen peroxide (H2O2) in biological systems is associated with a variety of pathologies including neurodegenerative diseases, cancer, and the general process of… (more)

Subjects/Keywords: Organic Chemistry; Cellular Biology; Biochemistry; fluorescence; Hydrogen peroxide; neural stem cells; reactive oxygen species; sensors

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APA (6th Edition):

Dickinson, B. C. (2010). Molecular Imaging Approaches to Understanding the Roles of Hydrogen Peroxide Biology in Stress and Development. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/07n8n80h

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):

Dickinson, Bryan Craig. “Molecular Imaging Approaches to Understanding the Roles of Hydrogen Peroxide Biology in Stress and Development.” 2010. Thesis, University of California – Berkeley. Accessed June 06, 2020. http://www.escholarship.org/uc/item/07n8n80h.

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

MLA Handbook (7th Edition):

Dickinson, Bryan Craig. “Molecular Imaging Approaches to Understanding the Roles of Hydrogen Peroxide Biology in Stress and Development.” 2010. Web. 06 Jun 2020.

Vancouver:

Dickinson BC. Molecular Imaging Approaches to Understanding the Roles of Hydrogen Peroxide Biology in Stress and Development. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2020 Jun 06]. Available from: http://www.escholarship.org/uc/item/07n8n80h.

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

Council of Science Editors:

Dickinson BC. Molecular Imaging Approaches to Understanding the Roles of Hydrogen Peroxide Biology in Stress and Development. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/07n8n80h

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


University of Western Ontario

15. Brown, Jason CL. Mitochondrial metabolic suppression and reactive oxygen species production during hypometabolism in mammals.

Degree: 2011, University of Western Ontario

 During hibernation, daily torpor, and fasting, mammals reduce metabolic rate (MR) up to 99%, 95%, and 30%, respectively, compared to resting levels. Mitochondrial metabolic suppression… (more)

Subjects/Keywords: hibernation; daily torpor; fasting; oxidative phosphorylation; reactive oxygen species; Biochemistry; Comparative and Evolutionary Physiology; Zoology

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APA (6th Edition):

Brown, J. C. (2011). Mitochondrial metabolic suppression and reactive oxygen species production during hypometabolism in mammals. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/208

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):

Brown, Jason CL. “Mitochondrial metabolic suppression and reactive oxygen species production during hypometabolism in mammals.” 2011. Thesis, University of Western Ontario. Accessed June 06, 2020. https://ir.lib.uwo.ca/etd/208.

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

MLA Handbook (7th Edition):

Brown, Jason CL. “Mitochondrial metabolic suppression and reactive oxygen species production during hypometabolism in mammals.” 2011. Web. 06 Jun 2020.

Vancouver:

Brown JC. Mitochondrial metabolic suppression and reactive oxygen species production during hypometabolism in mammals. [Internet] [Thesis]. University of Western Ontario; 2011. [cited 2020 Jun 06]. Available from: https://ir.lib.uwo.ca/etd/208.

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

Council of Science Editors:

Brown JC. Mitochondrial metabolic suppression and reactive oxygen species production during hypometabolism in mammals. [Thesis]. University of Western Ontario; 2011. Available from: https://ir.lib.uwo.ca/etd/208

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


University of Kansas

16. Tan, Ee Phie. O-GlcNAc Regulation of Mitochondrial Function and Energy Metabolism.

Degree: PhD, Biochemistry & Molecular Biology, 2017, University of Kansas

 O-GlcNAc is a post-translational modification (PTM) of a single N-acetylglucosamine sugar attachment on serine or threonine residues of nuclear, cytoplasmic, and mitochondrial proteins. Two opposing… (more)

Subjects/Keywords: Biochemistry; Metabolism; Mitochondrial function; O-GlcNAc; O-GlcNAcase; O-GlcNAc transferase; Reactive oxygen species

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APA (6th Edition):

Tan, E. P. (2017). O-GlcNAc Regulation of Mitochondrial Function and Energy Metabolism. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/26931

Chicago Manual of Style (16th Edition):

Tan, Ee Phie. “O-GlcNAc Regulation of Mitochondrial Function and Energy Metabolism.” 2017. Doctoral Dissertation, University of Kansas. Accessed June 06, 2020. http://hdl.handle.net/1808/26931.

MLA Handbook (7th Edition):

Tan, Ee Phie. “O-GlcNAc Regulation of Mitochondrial Function and Energy Metabolism.” 2017. Web. 06 Jun 2020.

Vancouver:

Tan EP. O-GlcNAc Regulation of Mitochondrial Function and Energy Metabolism. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1808/26931.

Council of Science Editors:

Tan EP. O-GlcNAc Regulation of Mitochondrial Function and Energy Metabolism. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/26931


University of Cincinnati

17. Bell-Horwath, Tiffany R. Derivation of Hydroquinone to Produce Selective, Oxidatively Activated Chemotherapeutic Agents.

Degree: PhD, Arts and Sciences: Chemistry, 2014, University of Cincinnati

 DNA modifying agents are stalwarts of chemotherapeutic cancer treatments, but require vital design improvements to improve selectivity, lower side effects, and continue their widespread use.… (more)

Subjects/Keywords: Biochemistry; Reactive Oxygen Species; AML; ROS; Anti-Cancer Agent; Drug Design; Acute Myeloid Leukemia

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APA (6th Edition):

Bell-Horwath, T. R. (2014). Derivation of Hydroquinone to Produce Selective, Oxidatively Activated Chemotherapeutic Agents. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1397736839

Chicago Manual of Style (16th Edition):

Bell-Horwath, Tiffany R. “Derivation of Hydroquinone to Produce Selective, Oxidatively Activated Chemotherapeutic Agents.” 2014. Doctoral Dissertation, University of Cincinnati. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1397736839.

MLA Handbook (7th Edition):

Bell-Horwath, Tiffany R. “Derivation of Hydroquinone to Produce Selective, Oxidatively Activated Chemotherapeutic Agents.” 2014. Web. 06 Jun 2020.

Vancouver:

Bell-Horwath TR. Derivation of Hydroquinone to Produce Selective, Oxidatively Activated Chemotherapeutic Agents. [Internet] [Doctoral dissertation]. University of Cincinnati; 2014. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1397736839.

Council of Science Editors:

Bell-Horwath TR. Derivation of Hydroquinone to Produce Selective, Oxidatively Activated Chemotherapeutic Agents. [Doctoral Dissertation]. University of Cincinnati; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1397736839


Wright State University

18. HOLLYFIELD, JENNIFER LYNNE. DOSE-DEPENDENT EFFECTS OF OXYGEN ON METABOLISM IN RAT CORTICO-HIPPOCAMPAL BRAIN TISSUE SLICES.

Degree: MS, Biochemistry and Molecular Biology, 2009, Wright State University

 Studies have shown that 95% oxygen increases neuronal excitability and ROS production. We wanted to investigate the dose-dependent effects of oxygen on brain slice metabolism.… (more)

Subjects/Keywords: Biochemistry; Biology; Biomedical Research; NMR; nuclear magnetic resonance; brain slices; hippocampus; oxygen

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APA (6th Edition):

HOLLYFIELD, J. L. (2009). DOSE-DEPENDENT EFFECTS OF OXYGEN ON METABOLISM IN RAT CORTICO-HIPPOCAMPAL BRAIN TISSUE SLICES. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1242417163

Chicago Manual of Style (16th Edition):

HOLLYFIELD, JENNIFER LYNNE. “DOSE-DEPENDENT EFFECTS OF OXYGEN ON METABOLISM IN RAT CORTICO-HIPPOCAMPAL BRAIN TISSUE SLICES.” 2009. Masters Thesis, Wright State University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1242417163.

MLA Handbook (7th Edition):

HOLLYFIELD, JENNIFER LYNNE. “DOSE-DEPENDENT EFFECTS OF OXYGEN ON METABOLISM IN RAT CORTICO-HIPPOCAMPAL BRAIN TISSUE SLICES.” 2009. Web. 06 Jun 2020.

Vancouver:

HOLLYFIELD JL. DOSE-DEPENDENT EFFECTS OF OXYGEN ON METABOLISM IN RAT CORTICO-HIPPOCAMPAL BRAIN TISSUE SLICES. [Internet] [Masters thesis]. Wright State University; 2009. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1242417163.

Council of Science Editors:

HOLLYFIELD JL. DOSE-DEPENDENT EFFECTS OF OXYGEN ON METABOLISM IN RAT CORTICO-HIPPOCAMPAL BRAIN TISSUE SLICES. [Masters Thesis]. Wright State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1242417163


University of Cincinnati

19. Thowfeik, Fathima Shazna. Targeting a Common Enemy: Toxic Cellular Mechanism of Novel Anti-cancer Agents that Alter DNA and Transcription.

Degree: PhD, Arts and Sciences: Chemistry, 2016, University of Cincinnati

 Cancer is a major public health problem in the worldwide and second leading cause of death in the United States. The major problem in treatment… (more)

Subjects/Keywords: Biochemistry; Reactive Oxygen Species; AML; mechanism of action; cytotoxicity; homologous recombination; HDAC8

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APA (6th Edition):

Thowfeik, F. S. (2016). Targeting a Common Enemy: Toxic Cellular Mechanism of Novel Anti-cancer Agents that Alter DNA and Transcription. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1460652655

Chicago Manual of Style (16th Edition):

Thowfeik, Fathima Shazna. “Targeting a Common Enemy: Toxic Cellular Mechanism of Novel Anti-cancer Agents that Alter DNA and Transcription.” 2016. Doctoral Dissertation, University of Cincinnati. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1460652655.

MLA Handbook (7th Edition):

Thowfeik, Fathima Shazna. “Targeting a Common Enemy: Toxic Cellular Mechanism of Novel Anti-cancer Agents that Alter DNA and Transcription.” 2016. Web. 06 Jun 2020.

Vancouver:

Thowfeik FS. Targeting a Common Enemy: Toxic Cellular Mechanism of Novel Anti-cancer Agents that Alter DNA and Transcription. [Internet] [Doctoral dissertation]. University of Cincinnati; 2016. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1460652655.

Council of Science Editors:

Thowfeik FS. Targeting a Common Enemy: Toxic Cellular Mechanism of Novel Anti-cancer Agents that Alter DNA and Transcription. [Doctoral Dissertation]. University of Cincinnati; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1460652655


University of Oxford

20. Feng, Tianshu. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.

Degree: PhD, 2014, University of Oxford

 Members of the 2-oxoglutarate (2OG)- and Fe(II)-dependent oxygenase (2OG oxygenase) superfamily catalyse a wide range of oxidative reactions in biology. 2OG oxygenases require Fe(II) and… (more)

Subjects/Keywords: 572; Biochemistry; Cell Biology; oxygen sensing; protein synthesis; translational termination; ribosome; post-translational modification

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APA (6th Edition):

Feng, T. (2014). Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026

Chicago Manual of Style (16th Edition):

Feng, Tianshu. “Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.” 2014. Doctoral Dissertation, University of Oxford. Accessed June 06, 2020. http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026.

MLA Handbook (7th Edition):

Feng, Tianshu. “Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus.” 2014. Web. 06 Jun 2020.

Vancouver:

Feng T. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2020 Jun 06]. Available from: http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026.

Council of Science Editors:

Feng T. Characterisation of 2-oxoglutarate- and fe(II)-dependent oxygenases targeting the protein synthesis apparatus. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:406a311b-dae6-48c6-9785-1e2f0b889e45 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655026


University of Michigan

21. Khobeir, Alexander Mikha. Quantifying the Effects of Common in vitro Cell Culture Techniques on Glutathione Depletion and Cellular Viability via Breast Cancer Cells and Reactive Oxygen Species (ROS).

Degree: MS, Chemistry and Biochemistry, 2016, University of Michigan

 Glutathione (GSH), an important antioxidant, is essential for proper mammalian biochemical function. Its mechanism as an antioxidant involves the neutralization of reactive oxygen species (ROS)… (more)

Subjects/Keywords: breast cancer; cell culture; glutathione; GSH; in vitro; reactive oxygen species (ROS); biochemistry

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APA (6th Edition):

Khobeir, A. M. (2016). Quantifying the Effects of Common in vitro Cell Culture Techniques on Glutathione Depletion and Cellular Viability via Breast Cancer Cells and Reactive Oxygen Species (ROS). (Masters Thesis). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/134400

Chicago Manual of Style (16th Edition):

Khobeir, Alexander Mikha. “Quantifying the Effects of Common in vitro Cell Culture Techniques on Glutathione Depletion and Cellular Viability via Breast Cancer Cells and Reactive Oxygen Species (ROS).” 2016. Masters Thesis, University of Michigan. Accessed June 06, 2020. http://hdl.handle.net/2027.42/134400.

MLA Handbook (7th Edition):

Khobeir, Alexander Mikha. “Quantifying the Effects of Common in vitro Cell Culture Techniques on Glutathione Depletion and Cellular Viability via Breast Cancer Cells and Reactive Oxygen Species (ROS).” 2016. Web. 06 Jun 2020.

Vancouver:

Khobeir AM. Quantifying the Effects of Common in vitro Cell Culture Techniques on Glutathione Depletion and Cellular Viability via Breast Cancer Cells and Reactive Oxygen Species (ROS). [Internet] [Masters thesis]. University of Michigan; 2016. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/2027.42/134400.

Council of Science Editors:

Khobeir AM. Quantifying the Effects of Common in vitro Cell Culture Techniques on Glutathione Depletion and Cellular Viability via Breast Cancer Cells and Reactive Oxygen Species (ROS). [Masters Thesis]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/134400


Western Washington University

22. Hubbard, Rachel J. (Rachel Joy). Progress Toward Strucutral Studies of a Circurlaly Permuted Human Hemoglobins Containing T-State Stabilizing Mutations.

Degree: MS, Chemistry, 2016, Western Washington University

  Our research is focused on the production of a hemoglobin based oxygen carrier (HBOC) which can be used as a therapeutic in the event… (more)

Subjects/Keywords: Chemistry; Hemoglobin – Synthesis; Blood substitutes; Oxygen – Physiological transport; Blood – Transfusion; Hemoglobin – Physiology; Biochemistry; masters theses

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APA (6th Edition):

Hubbard, R. J. (. J. (2016). Progress Toward Strucutral Studies of a Circurlaly Permuted Human Hemoglobins Containing T-State Stabilizing Mutations. (Masters Thesis). Western Washington University. Retrieved from https://cedar.wwu.edu/wwuet/468

Chicago Manual of Style (16th Edition):

Hubbard, Rachel J (Rachel Joy). “Progress Toward Strucutral Studies of a Circurlaly Permuted Human Hemoglobins Containing T-State Stabilizing Mutations.” 2016. Masters Thesis, Western Washington University. Accessed June 06, 2020. https://cedar.wwu.edu/wwuet/468.

MLA Handbook (7th Edition):

Hubbard, Rachel J (Rachel Joy). “Progress Toward Strucutral Studies of a Circurlaly Permuted Human Hemoglobins Containing T-State Stabilizing Mutations.” 2016. Web. 06 Jun 2020.

Vancouver:

Hubbard RJ(J. Progress Toward Strucutral Studies of a Circurlaly Permuted Human Hemoglobins Containing T-State Stabilizing Mutations. [Internet] [Masters thesis]. Western Washington University; 2016. [cited 2020 Jun 06]. Available from: https://cedar.wwu.edu/wwuet/468.

Council of Science Editors:

Hubbard RJ(J. Progress Toward Strucutral Studies of a Circurlaly Permuted Human Hemoglobins Containing T-State Stabilizing Mutations. [Masters Thesis]. Western Washington University; 2016. Available from: https://cedar.wwu.edu/wwuet/468


University of Arkansas

23. Alnasrawi, Abeer Muhammedali. Optimizing a Luciferase-Based Tool for Studying the Effects of Fatty Acid Desaturase 7 on Singlet Oxygen Accumulation in Arabidopsis thaliana.

Degree: MS, 2015, University of Arkansas

  In plants, reactive oxygen species (ROS) are generated as a byproduct of normal metabolism, as well as in response to adverse conditions such as… (more)

Subjects/Keywords: Biological sciences; Fatty acid desaturase 7; Singlet oxygen accumulation; Biochemistry; Molecular Biology; Plant Biology

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APA (6th Edition):

Alnasrawi, A. M. (2015). Optimizing a Luciferase-Based Tool for Studying the Effects of Fatty Acid Desaturase 7 on Singlet Oxygen Accumulation in Arabidopsis thaliana. (Masters Thesis). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/1319

Chicago Manual of Style (16th Edition):

Alnasrawi, Abeer Muhammedali. “Optimizing a Luciferase-Based Tool for Studying the Effects of Fatty Acid Desaturase 7 on Singlet Oxygen Accumulation in Arabidopsis thaliana.” 2015. Masters Thesis, University of Arkansas. Accessed June 06, 2020. https://scholarworks.uark.edu/etd/1319.

MLA Handbook (7th Edition):

Alnasrawi, Abeer Muhammedali. “Optimizing a Luciferase-Based Tool for Studying the Effects of Fatty Acid Desaturase 7 on Singlet Oxygen Accumulation in Arabidopsis thaliana.” 2015. Web. 06 Jun 2020.

Vancouver:

Alnasrawi AM. Optimizing a Luciferase-Based Tool for Studying the Effects of Fatty Acid Desaturase 7 on Singlet Oxygen Accumulation in Arabidopsis thaliana. [Internet] [Masters thesis]. University of Arkansas; 2015. [cited 2020 Jun 06]. Available from: https://scholarworks.uark.edu/etd/1319.

Council of Science Editors:

Alnasrawi AM. Optimizing a Luciferase-Based Tool for Studying the Effects of Fatty Acid Desaturase 7 on Singlet Oxygen Accumulation in Arabidopsis thaliana. [Masters Thesis]. University of Arkansas; 2015. Available from: https://scholarworks.uark.edu/etd/1319


Kent State University

24. Suarez Moreira, Edward. Vascular Biochemistry of Vitmain B12: Exploring the Relationship between Intracellular Cobalamin and Redox Status in Human Aortic Endothelial Cells.

Degree: PhD, College of Arts and Sciences / School of Biomedical Sciences, 2010, Kent State University

  <b>Abstract</b> Cobalamins (vitamin B12 derivatives) are essential cofactors for two enzymes in mammals: cytosolic methionine synthase and mitochondrial methylmalonyl-CoA mutase. In addition to its… (more)

Subjects/Keywords: Biochemistry; Biomedical Research; Cellular Biology; Vitamin B12; Cobalamin Metabolism; Oxidative Stress; Reactive Oxygen Species; Cobalamin Synthesis

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APA (6th Edition):

Suarez Moreira, E. (2010). Vascular Biochemistry of Vitmain B12: Exploring the Relationship between Intracellular Cobalamin and Redox Status in Human Aortic Endothelial Cells. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1270788182

Chicago Manual of Style (16th Edition):

Suarez Moreira, Edward. “Vascular Biochemistry of Vitmain B12: Exploring the Relationship between Intracellular Cobalamin and Redox Status in Human Aortic Endothelial Cells.” 2010. Doctoral Dissertation, Kent State University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1270788182.

MLA Handbook (7th Edition):

Suarez Moreira, Edward. “Vascular Biochemistry of Vitmain B12: Exploring the Relationship between Intracellular Cobalamin and Redox Status in Human Aortic Endothelial Cells.” 2010. Web. 06 Jun 2020.

Vancouver:

Suarez Moreira E. Vascular Biochemistry of Vitmain B12: Exploring the Relationship between Intracellular Cobalamin and Redox Status in Human Aortic Endothelial Cells. [Internet] [Doctoral dissertation]. Kent State University; 2010. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1270788182.

Council of Science Editors:

Suarez Moreira E. Vascular Biochemistry of Vitmain B12: Exploring the Relationship between Intracellular Cobalamin and Redox Status in Human Aortic Endothelial Cells. [Doctoral Dissertation]. Kent State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1270788182


Kent State University

25. McGuire, Karen M. Characterization of Apatone and Tolecine Induced Cell Death Mechanisms in Bladder and Ovarian Cancer.

Degree: PhD, College of Arts and Sciences / School of Biomedical Sciences, 2012, Kent State University

  McGuire, Karen M., Ph.D., May 2012, Biomedical Sciences Characterization of Apatone and Tolecine Induced Cell Death Mechanisms in Bladder and Ovarian Cancer. Directors of… (more)

Subjects/Keywords: Biochemistry; Biomedical Research; Cellular Biology; Apatone; Tolecine; bladder cancer; ovarian cancer; reactive oxygen species; oxidative stress; lysosome; mitochondria

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APA (6th Edition):

McGuire, K. M. (2012). Characterization of Apatone and Tolecine Induced Cell Death Mechanisms in Bladder and Ovarian Cancer. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1334356592

Chicago Manual of Style (16th Edition):

McGuire, Karen M. “Characterization of Apatone and Tolecine Induced Cell Death Mechanisms in Bladder and Ovarian Cancer.” 2012. Doctoral Dissertation, Kent State University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1334356592.

MLA Handbook (7th Edition):

McGuire, Karen M. “Characterization of Apatone and Tolecine Induced Cell Death Mechanisms in Bladder and Ovarian Cancer.” 2012. Web. 06 Jun 2020.

Vancouver:

McGuire KM. Characterization of Apatone and Tolecine Induced Cell Death Mechanisms in Bladder and Ovarian Cancer. [Internet] [Doctoral dissertation]. Kent State University; 2012. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1334356592.

Council of Science Editors:

McGuire KM. Characterization of Apatone and Tolecine Induced Cell Death Mechanisms in Bladder and Ovarian Cancer. [Doctoral Dissertation]. Kent State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1334356592


University of Toledo Health Science Campus

26. Nash, Kevin Michael. Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke.

Degree: PhD, Experimental Therapeutics, 2017, University of Toledo Health Science Campus

 Ischemic stroke is caused by a blockage of the blood flow to the brain resulting in neuronal and glial hypoxia leading to inflammatory and free… (more)

Subjects/Keywords: Pharmacology; Biochemistry; Neurobiology; Neurosciences; Organic Chemistry; Physical Chemistry; Nitrone; Reactive Oxygen Species; Nitric Oxide; Nitric Oxide Synthase; Stroke; Ischemia

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APA (6th Edition):

Nash, K. M. (2017). Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096

Chicago Manual of Style (16th Edition):

Nash, Kevin Michael. “Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke.” 2017. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096.

MLA Handbook (7th Edition):

Nash, Kevin Michael. “Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke.” 2017. Web. 06 Jun 2020.

Vancouver:

Nash KM. Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2017. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096.

Council of Science Editors:

Nash KM. Development of a Reactive Oxygen Species-Sensitive Nitric Oxide Synthase Inhibitor for the Treatment of Ischemic Stroke. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1512053682446096


University of Western Ontario

27. Youssef, Amer. The Role of Oxygen Tension and Insulin-Like Growth Factor Signaling in the Placental Mesenchymal Stem Cell Fate.

Degree: 2014, University of Western Ontario

 The human placenta of different gestational ages is a readily available source for isolation of adult mesenchymal stem cell (MSC) for potential use in regenerative… (more)

Subjects/Keywords: IGF; Stem Cells; Low oxygen tension; Niche; Multipotency; Differentiation; Biological Phenomena, Cell Phenomena, and Immunity; Cell Biology; Medical Biochemistry

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APA (6th Edition):

Youssef, A. (2014). The Role of Oxygen Tension and Insulin-Like Growth Factor Signaling in the Placental Mesenchymal Stem Cell Fate. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1885

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):

Youssef, Amer. “The Role of Oxygen Tension and Insulin-Like Growth Factor Signaling in the Placental Mesenchymal Stem Cell Fate.” 2014. Thesis, University of Western Ontario. Accessed June 06, 2020. https://ir.lib.uwo.ca/etd/1885.

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

MLA Handbook (7th Edition):

Youssef, Amer. “The Role of Oxygen Tension and Insulin-Like Growth Factor Signaling in the Placental Mesenchymal Stem Cell Fate.” 2014. Web. 06 Jun 2020.

Vancouver:

Youssef A. The Role of Oxygen Tension and Insulin-Like Growth Factor Signaling in the Placental Mesenchymal Stem Cell Fate. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2020 Jun 06]. Available from: https://ir.lib.uwo.ca/etd/1885.

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

Council of Science Editors:

Youssef A. The Role of Oxygen Tension and Insulin-Like Growth Factor Signaling in the Placental Mesenchymal Stem Cell Fate. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/1885

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


University of Edinburgh

28. Messenger, David James. Impact of UV light on the plant cell wall, methane emissions and ROS production.

Degree: PhD, 2009, University of Edinburgh

 This study presents the first attempt to combine the fields of ultraviolet (UV) photobiology, plant cell wall biochemistry, aerobic methane production and reactive oxygen species… (more)

Subjects/Keywords: 571.2; ultraviolet photobiology; UV radiation; vegetation foliage; plant cell wall biochemistry; aerobic methane production; reactive oxygen species; decomposition rates

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APA (6th Edition):

Messenger, D. J. (2009). Impact of UV light on the plant cell wall, methane emissions and ROS production. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4347

Chicago Manual of Style (16th Edition):

Messenger, David James. “Impact of UV light on the plant cell wall, methane emissions and ROS production.” 2009. Doctoral Dissertation, University of Edinburgh. Accessed June 06, 2020. http://hdl.handle.net/1842/4347.

MLA Handbook (7th Edition):

Messenger, David James. “Impact of UV light on the plant cell wall, methane emissions and ROS production.” 2009. Web. 06 Jun 2020.

Vancouver:

Messenger DJ. Impact of UV light on the plant cell wall, methane emissions and ROS production. [Internet] [Doctoral dissertation]. University of Edinburgh; 2009. [cited 2020 Jun 06]. Available from: http://hdl.handle.net/1842/4347.

Council of Science Editors:

Messenger DJ. Impact of UV light on the plant cell wall, methane emissions and ROS production. [Doctoral Dissertation]. University of Edinburgh; 2009. Available from: http://hdl.handle.net/1842/4347


Portland State University

29. Wagner, Mark Lowell. The physiology and biochemistry of isolated skeletal muscle mitochondria : a comparative study.

Degree: MS(M.S.) in Biology, Biology, 1989, Portland State University

  The physiological limit to maximum aerobic capacity (VO2max) in vertebrates has been attributed to cardiovascular oxygen delivery, to the ability of the muscle cells… (more)

Subjects/Keywords: Mitochondria; Oxygen in the body; Biochemistry; Physiology

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APA (6th Edition):

Wagner, M. L. (1989). The physiology and biochemistry of isolated skeletal muscle mitochondria : a comparative study. (Masters Thesis). Portland State University. Retrieved from https://pdxscholar.library.pdx.edu/open_access_etds/3956

Chicago Manual of Style (16th Edition):

Wagner, Mark Lowell. “The physiology and biochemistry of isolated skeletal muscle mitochondria : a comparative study.” 1989. Masters Thesis, Portland State University. Accessed June 06, 2020. https://pdxscholar.library.pdx.edu/open_access_etds/3956.

MLA Handbook (7th Edition):

Wagner, Mark Lowell. “The physiology and biochemistry of isolated skeletal muscle mitochondria : a comparative study.” 1989. Web. 06 Jun 2020.

Vancouver:

Wagner ML. The physiology and biochemistry of isolated skeletal muscle mitochondria : a comparative study. [Internet] [Masters thesis]. Portland State University; 1989. [cited 2020 Jun 06]. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/3956.

Council of Science Editors:

Wagner ML. The physiology and biochemistry of isolated skeletal muscle mitochondria : a comparative study. [Masters Thesis]. Portland State University; 1989. Available from: https://pdxscholar.library.pdx.edu/open_access_etds/3956


Youngstown State University

30. Mensah, Eric. Creation of a Site-Directed Mutant of Hen Egg White Lysozyme Working Toward Site-Specific Oxidation as it Relates to Protein Structure.

Degree: MSin Chemistry, Department of Chemistry, 2009, Youngstown State University

 Metal catalyzed oxidation of protein involves a reaction between hydrogen peroxide and protein-bound metal ions. Production of the highly-reactive hydroxyl radical leads to oxidative damage… (more)

Subjects/Keywords: Biochemistry; Organic Chemistry; protein expression; site-specific oxidation; site-directed mutagenesis; protein purification; protein modification; reactive oxygen species and disease state

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

APA (6th Edition):

Mensah, E. (2009). Creation of a Site-Directed Mutant of Hen Egg White Lysozyme Working Toward Site-Specific Oxidation as it Relates to Protein Structure. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1251756763

Chicago Manual of Style (16th Edition):

Mensah, Eric. “Creation of a Site-Directed Mutant of Hen Egg White Lysozyme Working Toward Site-Specific Oxidation as it Relates to Protein Structure.” 2009. Masters Thesis, Youngstown State University. Accessed June 06, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1251756763.

MLA Handbook (7th Edition):

Mensah, Eric. “Creation of a Site-Directed Mutant of Hen Egg White Lysozyme Working Toward Site-Specific Oxidation as it Relates to Protein Structure.” 2009. Web. 06 Jun 2020.

Vancouver:

Mensah E. Creation of a Site-Directed Mutant of Hen Egg White Lysozyme Working Toward Site-Specific Oxidation as it Relates to Protein Structure. [Internet] [Masters thesis]. Youngstown State University; 2009. [cited 2020 Jun 06]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1251756763.

Council of Science Editors:

Mensah E. Creation of a Site-Directed Mutant of Hen Egg White Lysozyme Working Toward Site-Specific Oxidation as it Relates to Protein Structure. [Masters Thesis]. Youngstown State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1251756763

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