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Dates: 2015 – 2019

You searched for subject:(AMINO SUGARS BIOCHEMISTRY ). Showing records 1 – 30 of 4940 total matches.

[1] [2] [3] [4] [5] … [165]

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University of Florida

1. Vanzomeren, Christine M. Biogeochemical Cycling of Organic Nitrogen in Subtropical Wetlands.

Degree: PhD, Soil and Water Science, 2015, University of Florida

 Wetlands are known to accrete organic nitrogen (N). Approximately 95% of soil total N is in the organic form. The main source of bioavailable N… (more)

Subjects/Keywords: Amino acids; Amino sugars; Canning jars; Everglades; Microbial biomass; Nitrogen; Soils; Vegetation; Vegetation types; Wetlands; acids  – amino  – nitrogen  – organic  – subtropical  – wetlands

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APA (6th Edition):

Vanzomeren, C. M. (2015). Biogeochemical Cycling of Organic Nitrogen in Subtropical Wetlands. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0047689

Chicago Manual of Style (16th Edition):

Vanzomeren, Christine M. “Biogeochemical Cycling of Organic Nitrogen in Subtropical Wetlands.” 2015. Doctoral Dissertation, University of Florida. Accessed December 16, 2019. http://ufdc.ufl.edu/UFE0047689.

MLA Handbook (7th Edition):

Vanzomeren, Christine M. “Biogeochemical Cycling of Organic Nitrogen in Subtropical Wetlands.” 2015. Web. 16 Dec 2019.

Vancouver:

Vanzomeren CM. Biogeochemical Cycling of Organic Nitrogen in Subtropical Wetlands. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2019 Dec 16]. Available from: http://ufdc.ufl.edu/UFE0047689.

Council of Science Editors:

Vanzomeren CM. Biogeochemical Cycling of Organic Nitrogen in Subtropical Wetlands. [Doctoral Dissertation]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/UFE0047689


University of Florida

2. Moye, Zachary D. Evolved for Adversity The Adaptation of Streptococcus Mutans to Environmental Carbohydrates.

Degree: PhD, Medical Sciences - Immunology and Microbiology (IDP), 2015, University of Florida

 Many human diseases arise due to shifts in the composition of the microbiome brought about by environmental fluctuations. In the case of dental caries, oral… (more)

Subjects/Keywords: Amino sugars; Biofilms; Enzymes; Gene expression; Metabolism; Operon; pH; Phosphates; Streptococcus mutans; Sugars; bacteria  – carbohydrates  – caries  – competence  – metabolism  – physiology

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APA (6th Edition):

Moye, Z. D. (2015). Evolved for Adversity The Adaptation of Streptococcus Mutans to Environmental Carbohydrates. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0049447

Chicago Manual of Style (16th Edition):

Moye, Zachary D. “Evolved for Adversity The Adaptation of Streptococcus Mutans to Environmental Carbohydrates.” 2015. Doctoral Dissertation, University of Florida. Accessed December 16, 2019. http://ufdc.ufl.edu/UFE0049447.

MLA Handbook (7th Edition):

Moye, Zachary D. “Evolved for Adversity The Adaptation of Streptococcus Mutans to Environmental Carbohydrates.” 2015. Web. 16 Dec 2019.

Vancouver:

Moye ZD. Evolved for Adversity The Adaptation of Streptococcus Mutans to Environmental Carbohydrates. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2019 Dec 16]. Available from: http://ufdc.ufl.edu/UFE0049447.

Council of Science Editors:

Moye ZD. Evolved for Adversity The Adaptation of Streptococcus Mutans to Environmental Carbohydrates. [Doctoral Dissertation]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/UFE0049447


Columbia University

3. Sanguineti, Gabriella. Novel Methods for the Ribosomal Incorporation of β-Amino Acids.

Degree: 2016, Columbia University

 Protein-protein interactions (PPIs) dominate all cellular functions across every domain of life. If PPIs become aberrant, they may result in many human diseases, such as… (more)

Subjects/Keywords: Amino acids; Biochemistry – Methodology; Peptides – Synthesis; Biochemistry

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APA (6th Edition):

Sanguineti, G. (2016). Novel Methods for the Ribosomal Incorporation of β-Amino Acids. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8H70FXK

Chicago Manual of Style (16th Edition):

Sanguineti, Gabriella. “Novel Methods for the Ribosomal Incorporation of β-Amino Acids.” 2016. Doctoral Dissertation, Columbia University. Accessed December 16, 2019. https://doi.org/10.7916/D8H70FXK.

MLA Handbook (7th Edition):

Sanguineti, Gabriella. “Novel Methods for the Ribosomal Incorporation of β-Amino Acids.” 2016. Web. 16 Dec 2019.

Vancouver:

Sanguineti G. Novel Methods for the Ribosomal Incorporation of β-Amino Acids. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2019 Dec 16]. Available from: https://doi.org/10.7916/D8H70FXK.

Council of Science Editors:

Sanguineti G. Novel Methods for the Ribosomal Incorporation of β-Amino Acids. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D8H70FXK


Columbia University

4. Fleisher, Rachel Chaya. Examining the Effects of D-Amino Acids on Translation.

Degree: 2016, Columbia University

 The ribosome is responsible for mRNA-templated protein translation in all living cells. The translational machinery (TM) has evolved to use 20 amino acids each esterified… (more)

Subjects/Keywords: Messenger RNA; Amino acids; Amino acid sequence; Ribosomes; Biochemistry; Chemistry

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APA (6th Edition):

Fleisher, R. C. (2016). Examining the Effects of D-Amino Acids on Translation. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8X92BH4

Chicago Manual of Style (16th Edition):

Fleisher, Rachel Chaya. “Examining the Effects of D-Amino Acids on Translation.” 2016. Doctoral Dissertation, Columbia University. Accessed December 16, 2019. https://doi.org/10.7916/D8X92BH4.

MLA Handbook (7th Edition):

Fleisher, Rachel Chaya. “Examining the Effects of D-Amino Acids on Translation.” 2016. Web. 16 Dec 2019.

Vancouver:

Fleisher RC. Examining the Effects of D-Amino Acids on Translation. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2019 Dec 16]. Available from: https://doi.org/10.7916/D8X92BH4.

Council of Science Editors:

Fleisher RC. Examining the Effects of D-Amino Acids on Translation. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D8X92BH4


University of Florida

5. Gilbert, Jessica L. Genetic, Environmental, and Sensory Variation in Southern Highbush Blueberry (Vaccinium corymbosum hybrids) Flavor.

Degree: PhD, Horticultural Sciences, 2015, University of Florida

 Blueberries are a high-value fruit that have experienced extraordinary growth in consumption in the past decade. Maintaining this growing market requires an understanding of the… (more)

Subjects/Keywords: Berries; Biochemistry; Blueberries; Breeding; Flavors; Fruits; Genotypes; Pentanones; Sweetness; Table sugars; blueberry  – flavor  – vaccinium  – volatiles

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APA (6th Edition):

Gilbert, J. L. (2015). Genetic, Environmental, and Sensory Variation in Southern Highbush Blueberry (Vaccinium corymbosum hybrids) Flavor. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0049167

Chicago Manual of Style (16th Edition):

Gilbert, Jessica L. “Genetic, Environmental, and Sensory Variation in Southern Highbush Blueberry (Vaccinium corymbosum hybrids) Flavor.” 2015. Doctoral Dissertation, University of Florida. Accessed December 16, 2019. http://ufdc.ufl.edu/UFE0049167.

MLA Handbook (7th Edition):

Gilbert, Jessica L. “Genetic, Environmental, and Sensory Variation in Southern Highbush Blueberry (Vaccinium corymbosum hybrids) Flavor.” 2015. Web. 16 Dec 2019.

Vancouver:

Gilbert JL. Genetic, Environmental, and Sensory Variation in Southern Highbush Blueberry (Vaccinium corymbosum hybrids) Flavor. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2019 Dec 16]. Available from: http://ufdc.ufl.edu/UFE0049167.

Council of Science Editors:

Gilbert JL. Genetic, Environmental, and Sensory Variation in Southern Highbush Blueberry (Vaccinium corymbosum hybrids) Flavor. [Doctoral Dissertation]. University of Florida; 2015. Available from: http://ufdc.ufl.edu/UFE0049167


University of California – Irvine

6. Spencer, Ryan Kelly. X-ray Crystallographic Studies of Oligomers Derived from Amyloidogenic Peptides and Proteins.

Degree: Chemistry, 2015, University of California – Irvine

 This dissertation describes a new class of macrocylic peptides which I invented as a tool for understanding the folding of beta-sheets and the structures of… (more)

Subjects/Keywords: Chemistry; Biochemistry; amyloid; N-methyl amino acids; oligomers; peptide crystallography; peptides

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APA (6th Edition):

Spencer, R. K. (2015). X-ray Crystallographic Studies of Oligomers Derived from Amyloidogenic Peptides and Proteins. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/3j88n15f

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):

Spencer, Ryan Kelly. “X-ray Crystallographic Studies of Oligomers Derived from Amyloidogenic Peptides and Proteins.” 2015. Thesis, University of California – Irvine. Accessed December 16, 2019. http://www.escholarship.org/uc/item/3j88n15f.

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

MLA Handbook (7th Edition):

Spencer, Ryan Kelly. “X-ray Crystallographic Studies of Oligomers Derived from Amyloidogenic Peptides and Proteins.” 2015. Web. 16 Dec 2019.

Vancouver:

Spencer RK. X-ray Crystallographic Studies of Oligomers Derived from Amyloidogenic Peptides and Proteins. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2019 Dec 16]. Available from: http://www.escholarship.org/uc/item/3j88n15f.

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

Council of Science Editors:

Spencer RK. X-ray Crystallographic Studies of Oligomers Derived from Amyloidogenic Peptides and Proteins. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/3j88n15f

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

7. Ley, Nathan Benjamin. Investigations into fragment ligand binding using quantitative STD and WaterLOGSY NMR spectroscopy.

Degree: PhD, 2015, University of Kent

 Ligand-observed NMR spectroscopy is frequently employed in early-stage drug discovery, often as an initial screen to narrow the field of potential drug-like molecules. However, its… (more)

Subjects/Keywords: 500; QD431 Organic Chemistry- Biochemistry- Proteins; peptides; amino acids

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APA (6th Edition):

Ley, N. B. (2015). Investigations into fragment ligand binding using quantitative STD and WaterLOGSY NMR spectroscopy. (Doctoral Dissertation). University of Kent. Retrieved from https://kar.kent.ac.uk/50197/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.659558

Chicago Manual of Style (16th Edition):

Ley, Nathan Benjamin. “Investigations into fragment ligand binding using quantitative STD and WaterLOGSY NMR spectroscopy.” 2015. Doctoral Dissertation, University of Kent. Accessed December 16, 2019. https://kar.kent.ac.uk/50197/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.659558.

MLA Handbook (7th Edition):

Ley, Nathan Benjamin. “Investigations into fragment ligand binding using quantitative STD and WaterLOGSY NMR spectroscopy.” 2015. Web. 16 Dec 2019.

Vancouver:

Ley NB. Investigations into fragment ligand binding using quantitative STD and WaterLOGSY NMR spectroscopy. [Internet] [Doctoral dissertation]. University of Kent; 2015. [cited 2019 Dec 16]. Available from: https://kar.kent.ac.uk/50197/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.659558.

Council of Science Editors:

Ley NB. Investigations into fragment ligand binding using quantitative STD and WaterLOGSY NMR spectroscopy. [Doctoral Dissertation]. University of Kent; 2015. Available from: https://kar.kent.ac.uk/50197/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.659558


University of Pennsylvania

8. Walters, Christopher Russell. Improving The Usage Of Unnatural Amino Acids In Proteins: Thioamides And Other Biophysical Probes.

Degree: 2017, University of Pennsylvania

 Methods for genetically and synthetically manipulating protein composition enable a greater flexibility in the study of protein dynamics and function. However, current techniques for incorporating… (more)

Subjects/Keywords: Amino Acids; Biophysics; Chemical Biology; Proteins; Thioamides; Biochemistry; Chemistry

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APA (6th Edition):

Walters, C. R. (2017). Improving The Usage Of Unnatural Amino Acids In Proteins: Thioamides And Other Biophysical Probes. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2981

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):

Walters, Christopher Russell. “Improving The Usage Of Unnatural Amino Acids In Proteins: Thioamides And Other Biophysical Probes.” 2017. Thesis, University of Pennsylvania. Accessed December 16, 2019. https://repository.upenn.edu/edissertations/2981.

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

MLA Handbook (7th Edition):

Walters, Christopher Russell. “Improving The Usage Of Unnatural Amino Acids In Proteins: Thioamides And Other Biophysical Probes.” 2017. Web. 16 Dec 2019.

Vancouver:

Walters CR. Improving The Usage Of Unnatural Amino Acids In Proteins: Thioamides And Other Biophysical Probes. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2019 Dec 16]. Available from: https://repository.upenn.edu/edissertations/2981.

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

Council of Science Editors:

Walters CR. Improving The Usage Of Unnatural Amino Acids In Proteins: Thioamides And Other Biophysical Probes. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2981

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


University of Toledo

9. Dahal, Gopal Prasad. Development of Selective Inhibitors against Enzymes Involved in the Aspartate Biosynthetic Pathway for Antifungal Drug Development.

Degree: PhD, Chemistry, 2018, University of Toledo

 Aspartate semialdehyde dehydrogenase (ASADH) functions at a critical junction in the aspartate biosynthetic pathway and represents a validated target for antimicrobial drug design. This enzyme… (more)

Subjects/Keywords: Biophysics; Biochemistry; Chemistry; Antifungal drugs, amino acid biosynthesis, crystallography, drug design

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APA (6th Edition):

Dahal, G. P. (2018). Development of Selective Inhibitors against Enzymes Involved in the Aspartate Biosynthetic Pathway for Antifungal Drug Development. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1532889045486984

Chicago Manual of Style (16th Edition):

Dahal, Gopal Prasad. “Development of Selective Inhibitors against Enzymes Involved in the Aspartate Biosynthetic Pathway for Antifungal Drug Development.” 2018. Doctoral Dissertation, University of Toledo. Accessed December 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1532889045486984.

MLA Handbook (7th Edition):

Dahal, Gopal Prasad. “Development of Selective Inhibitors against Enzymes Involved in the Aspartate Biosynthetic Pathway for Antifungal Drug Development.” 2018. Web. 16 Dec 2019.

Vancouver:

Dahal GP. Development of Selective Inhibitors against Enzymes Involved in the Aspartate Biosynthetic Pathway for Antifungal Drug Development. [Internet] [Doctoral dissertation]. University of Toledo; 2018. [cited 2019 Dec 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1532889045486984.

Council of Science Editors:

Dahal GP. Development of Selective Inhibitors against Enzymes Involved in the Aspartate Biosynthetic Pathway for Antifungal Drug Development. [Doctoral Dissertation]. University of Toledo; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1532889045486984


University of Alberta

10. Hincapie Martinez, Daylin J. Glucosamine and Glucosamine-Peptides Antimicrobial Compounds.

Degree: MS, Department of Agricultural, Food, and Nutritional Science, 2015, University of Alberta

 Bacterial resistance to chemical and physical methods in food processing, and the consumers’ demand for food free of chemical additives challenge the food industry to… (more)

Subjects/Keywords: α-dicarbonyls; Amino sugars; Maillard reaction; iron; glucosamine; heat resistant E. coli; affinity chromatography; glycosylation; glycopeptides; antimicrobial activity; fish gelatin peptides; glycation

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APA (6th Edition):

Hincapie Martinez, D. J. (2015). Glucosamine and Glucosamine-Peptides Antimicrobial Compounds. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/n009w501p

Chicago Manual of Style (16th Edition):

Hincapie Martinez, Daylin J. “Glucosamine and Glucosamine-Peptides Antimicrobial Compounds.” 2015. Masters Thesis, University of Alberta. Accessed December 16, 2019. https://era.library.ualberta.ca/files/n009w501p.

MLA Handbook (7th Edition):

Hincapie Martinez, Daylin J. “Glucosamine and Glucosamine-Peptides Antimicrobial Compounds.” 2015. Web. 16 Dec 2019.

Vancouver:

Hincapie Martinez DJ. Glucosamine and Glucosamine-Peptides Antimicrobial Compounds. [Internet] [Masters thesis]. University of Alberta; 2015. [cited 2019 Dec 16]. Available from: https://era.library.ualberta.ca/files/n009w501p.

Council of Science Editors:

Hincapie Martinez DJ. Glucosamine and Glucosamine-Peptides Antimicrobial Compounds. [Masters Thesis]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/n009w501p

11. Alshamrani, Mona S. A Comprehensive Analysis of Aromatic-Proton Mediated Hydrogen Bonds.

Degree: MS, Chemistry and Biochemistry, 2018, South Dakota State University

  Hydrogen bonds play critical role in folding, structure and recognition of biological macromolecules (e.g., proteins, RNA, DNA). In addition to classical hydrogen bonds (e.g.,… (more)

Subjects/Keywords: amino acids; aromatic protons; bonds geometry; chemistry; hydrogen bonds; R and Perl; Biochemistry; Chemistry

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APA (6th Edition):

Alshamrani, M. S. (2018). A Comprehensive Analysis of Aromatic-Proton Mediated Hydrogen Bonds. (Masters Thesis). South Dakota State University. Retrieved from https://openprairie.sdstate.edu/etd/2434

Chicago Manual of Style (16th Edition):

Alshamrani, Mona S. “A Comprehensive Analysis of Aromatic-Proton Mediated Hydrogen Bonds.” 2018. Masters Thesis, South Dakota State University. Accessed December 16, 2019. https://openprairie.sdstate.edu/etd/2434.

MLA Handbook (7th Edition):

Alshamrani, Mona S. “A Comprehensive Analysis of Aromatic-Proton Mediated Hydrogen Bonds.” 2018. Web. 16 Dec 2019.

Vancouver:

Alshamrani MS. A Comprehensive Analysis of Aromatic-Proton Mediated Hydrogen Bonds. [Internet] [Masters thesis]. South Dakota State University; 2018. [cited 2019 Dec 16]. Available from: https://openprairie.sdstate.edu/etd/2434.

Council of Science Editors:

Alshamrani MS. A Comprehensive Analysis of Aromatic-Proton Mediated Hydrogen Bonds. [Masters Thesis]. South Dakota State University; 2018. Available from: https://openprairie.sdstate.edu/etd/2434

12. McMahon, Rachel M. Advances in Amino Acid Analysis for Marine Related Matrices and Its Application to Coastal Shelf Settings in The Canadian Arctic.

Degree: MS, Ocean/Earth/Atmos Sciences, 2018, Old Dominion University

Amino acids comprise up to 50% of organic matter in cellular material and are a major fraction of oceanic organic carbon. Amino acids are… (more)

Subjects/Keywords: Amino acids; Arctic Ocean; Biomarkers; LC-MS; Analytical Chemistry; Biochemistry; Geochemistry; Oceanography; Organic Chemistry

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APA (6th Edition):

McMahon, R. M. (2018). Advances in Amino Acid Analysis for Marine Related Matrices and Its Application to Coastal Shelf Settings in The Canadian Arctic. (Thesis). Old Dominion University. Retrieved from 9780438538306 ; https://digitalcommons.odu.edu/oeas_etds/14

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):

McMahon, Rachel M. “Advances in Amino Acid Analysis for Marine Related Matrices and Its Application to Coastal Shelf Settings in The Canadian Arctic.” 2018. Thesis, Old Dominion University. Accessed December 16, 2019. 9780438538306 ; https://digitalcommons.odu.edu/oeas_etds/14.

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

MLA Handbook (7th Edition):

McMahon, Rachel M. “Advances in Amino Acid Analysis for Marine Related Matrices and Its Application to Coastal Shelf Settings in The Canadian Arctic.” 2018. Web. 16 Dec 2019.

Vancouver:

McMahon RM. Advances in Amino Acid Analysis for Marine Related Matrices and Its Application to Coastal Shelf Settings in The Canadian Arctic. [Internet] [Thesis]. Old Dominion University; 2018. [cited 2019 Dec 16]. Available from: 9780438538306 ; https://digitalcommons.odu.edu/oeas_etds/14.

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

Council of Science Editors:

McMahon RM. Advances in Amino Acid Analysis for Marine Related Matrices and Its Application to Coastal Shelf Settings in The Canadian Arctic. [Thesis]. Old Dominion University; 2018. Available from: 9780438538306 ; https://digitalcommons.odu.edu/oeas_etds/14

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


University of Colorado

13. McKercher, Marissa A. Multimodal Recognition of Diverse Peptides by the SH2 Domains of PLCγ1 and SH2B1.

Degree: PhD, 2018, University of Colorado

 SH2 domains recognize phosphotyrosine (pY)-containing peptide ligands and regulate a wide array of signaling events within receptor tyrosine kinase pathways. SH2 domains have individualized specificity… (more)

Subjects/Keywords: phosphotyrosine; src homology 2 domain; peptides; hydrophobic; amino acids; Biochemistry; Molecular Biology

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APA (6th Edition):

McKercher, M. A. (2018). Multimodal Recognition of Diverse Peptides by the SH2 Domains of PLCγ1 and SH2B1. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/272

Chicago Manual of Style (16th Edition):

McKercher, Marissa A. “Multimodal Recognition of Diverse Peptides by the SH2 Domains of PLCγ1 and SH2B1.” 2018. Doctoral Dissertation, University of Colorado. Accessed December 16, 2019. https://scholar.colorado.edu/chem_gradetds/272.

MLA Handbook (7th Edition):

McKercher, Marissa A. “Multimodal Recognition of Diverse Peptides by the SH2 Domains of PLCγ1 and SH2B1.” 2018. Web. 16 Dec 2019.

Vancouver:

McKercher MA. Multimodal Recognition of Diverse Peptides by the SH2 Domains of PLCγ1 and SH2B1. [Internet] [Doctoral dissertation]. University of Colorado; 2018. [cited 2019 Dec 16]. Available from: https://scholar.colorado.edu/chem_gradetds/272.

Council of Science Editors:

McKercher MA. Multimodal Recognition of Diverse Peptides by the SH2 Domains of PLCγ1 and SH2B1. [Doctoral Dissertation]. University of Colorado; 2018. Available from: https://scholar.colorado.edu/chem_gradetds/272


University of Pennsylvania

14. Hostetler, Zachary Michael. A Genetically Encoded Fluorescent Amino Acid Reveals Protein Dynamics Regulating The Bacterial Dna Damage Response.

Degree: 2018, University of Pennsylvania

 Diversification of the genetic code in response to selective pressures can render organisms more fit to particular stresses. In many bacteria, the inducible prokaryotic DNA… (more)

Subjects/Keywords: Antibiotic Resistance; Fluorescence; Genetic Code Expansion; LexA; SOS Response; Unnatural Amino Acids; Biochemistry; Biophysics; Microbiology

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APA (6th Edition):

Hostetler, Z. M. (2018). A Genetically Encoded Fluorescent Amino Acid Reveals Protein Dynamics Regulating The Bacterial Dna Damage Response. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3129

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):

Hostetler, Zachary Michael. “A Genetically Encoded Fluorescent Amino Acid Reveals Protein Dynamics Regulating The Bacterial Dna Damage Response.” 2018. Thesis, University of Pennsylvania. Accessed December 16, 2019. https://repository.upenn.edu/edissertations/3129.

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

MLA Handbook (7th Edition):

Hostetler, Zachary Michael. “A Genetically Encoded Fluorescent Amino Acid Reveals Protein Dynamics Regulating The Bacterial Dna Damage Response.” 2018. Web. 16 Dec 2019.

Vancouver:

Hostetler ZM. A Genetically Encoded Fluorescent Amino Acid Reveals Protein Dynamics Regulating The Bacterial Dna Damage Response. [Internet] [Thesis]. University of Pennsylvania; 2018. [cited 2019 Dec 16]. Available from: https://repository.upenn.edu/edissertations/3129.

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

Council of Science Editors:

Hostetler ZM. A Genetically Encoded Fluorescent Amino Acid Reveals Protein Dynamics Regulating The Bacterial Dna Damage Response. [Thesis]. University of Pennsylvania; 2018. Available from: https://repository.upenn.edu/edissertations/3129

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

15. Knappenberger, Andrew John. MOLECULAR DRIVERS OF SPECIFICITY IN HUMAN RIBONUCLEOTIDE REDUCTASE.

Degree: PhD, Biochemistry, 2017, Case Western Reserve University School of Graduate Studies

 Ribonucleotide reductase (RR) enables organisms to grow and reproduce by providing the deoxynucleotides necessary for DNA replication. Human RR can reduce any of the four… (more)

Subjects/Keywords: Biochemistry; allosteric regulation; amino acid; biochemistry; enzyme; high performance liquid chromatography; mutagenesis; nucleotide analog; nucleotide metabolism; molecular evolution; phylogenetics

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APA (6th Edition):

Knappenberger, A. J. (2017). MOLECULAR DRIVERS OF SPECIFICITY IN HUMAN RIBONUCLEOTIDE REDUCTASE. (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1490722285574706

Chicago Manual of Style (16th Edition):

Knappenberger, Andrew John. “MOLECULAR DRIVERS OF SPECIFICITY IN HUMAN RIBONUCLEOTIDE REDUCTASE.” 2017. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed December 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1490722285574706.

MLA Handbook (7th Edition):

Knappenberger, Andrew John. “MOLECULAR DRIVERS OF SPECIFICITY IN HUMAN RIBONUCLEOTIDE REDUCTASE.” 2017. Web. 16 Dec 2019.

Vancouver:

Knappenberger AJ. MOLECULAR DRIVERS OF SPECIFICITY IN HUMAN RIBONUCLEOTIDE REDUCTASE. [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2017. [cited 2019 Dec 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1490722285574706.

Council of Science Editors:

Knappenberger AJ. MOLECULAR DRIVERS OF SPECIFICITY IN HUMAN RIBONUCLEOTIDE REDUCTASE. [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1490722285574706


Arizona State University

16. Mohan, Chitra. Effects of Physical Activity on the Performance of 24-h Urinary Sucrose and Fructose as a Biomarker of Total Sugars Intake.

Degree: Nutrition, 2019, Arizona State University

 Urinary sucrose and fructose has been suggested as a predictive biomarker of total sugars intake based on research involving UK adults. The purpose of this… (more)

Subjects/Keywords: Nutrition; 24-hour urine sugars biomarker; fructose; sucrose; sugars biomarker and physical activity; sugars consumption; sugars intake; sugars intake and physical activity; sugars consumption and physical activity; sugars urinary biomarker

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APA (6th Edition):

Mohan, C. (2019). Effects of Physical Activity on the Performance of 24-h Urinary Sucrose and Fructose as a Biomarker of Total Sugars Intake. (Masters Thesis). Arizona State University. Retrieved from http://repository.asu.edu/items/53467

Chicago Manual of Style (16th Edition):

Mohan, Chitra. “Effects of Physical Activity on the Performance of 24-h Urinary Sucrose and Fructose as a Biomarker of Total Sugars Intake.” 2019. Masters Thesis, Arizona State University. Accessed December 16, 2019. http://repository.asu.edu/items/53467.

MLA Handbook (7th Edition):

Mohan, Chitra. “Effects of Physical Activity on the Performance of 24-h Urinary Sucrose and Fructose as a Biomarker of Total Sugars Intake.” 2019. Web. 16 Dec 2019.

Vancouver:

Mohan C. Effects of Physical Activity on the Performance of 24-h Urinary Sucrose and Fructose as a Biomarker of Total Sugars Intake. [Internet] [Masters thesis]. Arizona State University; 2019. [cited 2019 Dec 16]. Available from: http://repository.asu.edu/items/53467.

Council of Science Editors:

Mohan C. Effects of Physical Activity on the Performance of 24-h Urinary Sucrose and Fructose as a Biomarker of Total Sugars Intake. [Masters Thesis]. Arizona State University; 2019. Available from: http://repository.asu.edu/items/53467


University of California – San Diego

17. Wang, Vivian. Genetic Incorporation of a Metal-chelating Unnatural Amino Acid and NMR Studies of the Viroporin p7 from Hepatitis C Virus.

Degree: Chemistry, 2015, University of California – San Diego

 Hepatitis C virus (HCV) proteins are targets for potential pharmaceutical drugs since there are currently no vaccines against the virus, and drug treatments are expensive… (more)

Subjects/Keywords: Biochemistry; Biophysics; Analytical chemistry; 2-amino-3-(8-hydroxyquinolin-3-yl)propanoic acid; hepatitis c virus; membrane protein; nuclear magnetic resonance; p7; unnatural amino acid

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APA (6th Edition):

Wang, V. (2015). Genetic Incorporation of a Metal-chelating Unnatural Amino Acid and NMR Studies of the Viroporin p7 from Hepatitis C Virus. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/6sj1p43k

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):

Wang, Vivian. “Genetic Incorporation of a Metal-chelating Unnatural Amino Acid and NMR Studies of the Viroporin p7 from Hepatitis C Virus.” 2015. Thesis, University of California – San Diego. Accessed December 16, 2019. http://www.escholarship.org/uc/item/6sj1p43k.

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

MLA Handbook (7th Edition):

Wang, Vivian. “Genetic Incorporation of a Metal-chelating Unnatural Amino Acid and NMR Studies of the Viroporin p7 from Hepatitis C Virus.” 2015. Web. 16 Dec 2019.

Vancouver:

Wang V. Genetic Incorporation of a Metal-chelating Unnatural Amino Acid and NMR Studies of the Viroporin p7 from Hepatitis C Virus. [Internet] [Thesis]. University of California – San Diego; 2015. [cited 2019 Dec 16]. Available from: http://www.escholarship.org/uc/item/6sj1p43k.

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

Council of Science Editors:

Wang V. Genetic Incorporation of a Metal-chelating Unnatural Amino Acid and NMR Studies of the Viroporin p7 from Hepatitis C Virus. [Thesis]. University of California – San Diego; 2015. Available from: http://www.escholarship.org/uc/item/6sj1p43k

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


University of Louisville

18. Nevitt, Christopher David. Alpha-amino methylation and acetylation are novel regulators of MYL9 function.

Degree: PhD, 2018, University of Louisville

  Dysregulation of alpha-amino post-translational modifications (Nα-PTMs) is found in multiple cancers and developmental disorders. However, the exact roles Nα-PTMs play in regulating protein function… (more)

Subjects/Keywords: alpha-amino PTM; protein methylation; acetylation; regulatory light chain; non-muscle myosin; compartmentalization; Amino Acids, Peptides, and Proteins; Biochemical Phenomena, Metabolism, and Nutrition; Biological Factors; Medical Biochemistry

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APA (6th Edition):

Nevitt, C. D. (2018). Alpha-amino methylation and acetylation are novel regulators of MYL9 function. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/3032 ; https://ir.library.louisville.edu/etd/3032

Chicago Manual of Style (16th Edition):

Nevitt, Christopher David. “Alpha-amino methylation and acetylation are novel regulators of MYL9 function.” 2018. Doctoral Dissertation, University of Louisville. Accessed December 16, 2019. 10.18297/etd/3032 ; https://ir.library.louisville.edu/etd/3032.

MLA Handbook (7th Edition):

Nevitt, Christopher David. “Alpha-amino methylation and acetylation are novel regulators of MYL9 function.” 2018. Web. 16 Dec 2019.

Vancouver:

Nevitt CD. Alpha-amino methylation and acetylation are novel regulators of MYL9 function. [Internet] [Doctoral dissertation]. University of Louisville; 2018. [cited 2019 Dec 16]. Available from: 10.18297/etd/3032 ; https://ir.library.louisville.edu/etd/3032.

Council of Science Editors:

Nevitt CD. Alpha-amino methylation and acetylation are novel regulators of MYL9 function. [Doctoral Dissertation]. University of Louisville; 2018. Available from: 10.18297/etd/3032 ; https://ir.library.louisville.edu/etd/3032


University of Manchester

19. Callagy, Sandra. An Investigation into Changes to Trace Metals and Metabolic Profiling in the Diabetic Retina.

Degree: 2018, University of Manchester

 Diabetes mellitus currently affects over 422 million people globally and over 80% of patients with diabetes will develop diabetic retinopathy. Patients with diabetic retinopathy initially… (more)

Subjects/Keywords: diabetes; diabetic; retinopathy; diabetic retinopathy; metabolomics; metabolic profiling; GC-MS; LC-MS; ICP-MS; metallomics; copper; copper dysregulation; ophthalmology; retina; glucose; mass spectrometry; rt-qPCR; streptozotocin; lipidomics; lipid profiling; amino acids; sugars; copper chelator; ratinopathy

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APA (6th Edition):

Callagy, S. (2018). An Investigation into Changes to Trace Metals and Metabolic Profiling in the Diabetic Retina. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313289

Chicago Manual of Style (16th Edition):

Callagy, Sandra. “An Investigation into Changes to Trace Metals and Metabolic Profiling in the Diabetic Retina.” 2018. Doctoral Dissertation, University of Manchester. Accessed December 16, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313289.

MLA Handbook (7th Edition):

Callagy, Sandra. “An Investigation into Changes to Trace Metals and Metabolic Profiling in the Diabetic Retina.” 2018. Web. 16 Dec 2019.

Vancouver:

Callagy S. An Investigation into Changes to Trace Metals and Metabolic Profiling in the Diabetic Retina. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Dec 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313289.

Council of Science Editors:

Callagy S. An Investigation into Changes to Trace Metals and Metabolic Profiling in the Diabetic Retina. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313289


University of Manchester

20. Callagy, Sandra. An investigation into changes to trace metals and metabolic profiling in the diabetic retina.

Degree: PhD, 2018, University of Manchester

 Diabetes mellitus currently affects over 422 million people globally and over 80% of patients with diabetes will develop diabetic retinopathy. Patients with diabetic retinopathy initially… (more)

Subjects/Keywords: mass spectrometry; rt-qPCR; streptozotocin; lipidomics; metabolic profiling; amino acids; sugars; copper chelator; ratinopathy; glucose; lipid profiling; retina; retinopathy; copper dysregulation; diabetes; diabetic; ophthalmology; metabolomics; diabetic retinopathy; LC-MS; ICP-MS; metallomics; copper; GC-MS

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APA (6th Edition):

Callagy, S. (2018). An investigation into changes to trace metals and metabolic profiling in the diabetic retina. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-changes-to-trace-metals-and-metabolic-profiling-in-the-diabetic-retina(213607b0-2a34-490a-bb17-2e08435eb446).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740329

Chicago Manual of Style (16th Edition):

Callagy, Sandra. “An investigation into changes to trace metals and metabolic profiling in the diabetic retina.” 2018. Doctoral Dissertation, University of Manchester. Accessed December 16, 2019. https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-changes-to-trace-metals-and-metabolic-profiling-in-the-diabetic-retina(213607b0-2a34-490a-bb17-2e08435eb446).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740329.

MLA Handbook (7th Edition):

Callagy, Sandra. “An investigation into changes to trace metals and metabolic profiling in the diabetic retina.” 2018. Web. 16 Dec 2019.

Vancouver:

Callagy S. An investigation into changes to trace metals and metabolic profiling in the diabetic retina. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Dec 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-changes-to-trace-metals-and-metabolic-profiling-in-the-diabetic-retina(213607b0-2a34-490a-bb17-2e08435eb446).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740329.

Council of Science Editors:

Callagy S. An investigation into changes to trace metals and metabolic profiling in the diabetic retina. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/an-investigation-into-changes-to-trace-metals-and-metabolic-profiling-in-the-diabetic-retina(213607b0-2a34-490a-bb17-2e08435eb446).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740329


University of Kansas

21. Bishop, Stephanie Cara. Development of Novel Fluorescence and NMR Reagents for Monitoring Protein-Protein Interactions Between Survivin and Its Protein Binding Partners.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2015, University of Kansas

 Inhibition of protein-protein interactions is a promising therapeutic strategy for targeting non-enzymatic proteins. One strategy to inhibit protein-protein interactions is to design inhibitors specifically toward… (more)

Subjects/Keywords: Pharmacology; Biochemistry; Organic chemistry; Copper-free click chemistry; Fluorescence; Lanthanide chelation; Nuclear Magnetic Resonance; Paramagnetism; Unnatural Amino Acid Incorporation

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APA (6th Edition):

Bishop, S. C. (2015). Development of Novel Fluorescence and NMR Reagents for Monitoring Protein-Protein Interactions Between Survivin and Its Protein Binding Partners. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/19468

Chicago Manual of Style (16th Edition):

Bishop, Stephanie Cara. “Development of Novel Fluorescence and NMR Reagents for Monitoring Protein-Protein Interactions Between Survivin and Its Protein Binding Partners.” 2015. Doctoral Dissertation, University of Kansas. Accessed December 16, 2019. http://hdl.handle.net/1808/19468.

MLA Handbook (7th Edition):

Bishop, Stephanie Cara. “Development of Novel Fluorescence and NMR Reagents for Monitoring Protein-Protein Interactions Between Survivin and Its Protein Binding Partners.” 2015. Web. 16 Dec 2019.

Vancouver:

Bishop SC. Development of Novel Fluorescence and NMR Reagents for Monitoring Protein-Protein Interactions Between Survivin and Its Protein Binding Partners. [Internet] [Doctoral dissertation]. University of Kansas; 2015. [cited 2019 Dec 16]. Available from: http://hdl.handle.net/1808/19468.

Council of Science Editors:

Bishop SC. Development of Novel Fluorescence and NMR Reagents for Monitoring Protein-Protein Interactions Between Survivin and Its Protein Binding Partners. [Doctoral Dissertation]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/19468

22. Duffy, Caroline M. Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry and Molecular Pharmacology, 2016, U of Massachusetts : Med

  Chromosomal replication is an essential process in all life. This dissertation highlights regulatory roles for two critical protein complexes at the heart of the… (more)

Subjects/Keywords: DNA Replication; DNA-Binding Proteins; DNA Primers; Amino Acids, Peptides, and Proteins; Biochemistry; Molecular Biology; Structural Biology

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APA (6th Edition):

Duffy, C. M. (2016). Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/844

Chicago Manual of Style (16th Edition):

Duffy, Caroline M. “Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation.” 2016. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 16, 2019. http://escholarship.umassmed.edu/gsbs_diss/844.

MLA Handbook (7th Edition):

Duffy, Caroline M. “Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation.” 2016. Web. 16 Dec 2019.

Vancouver:

Duffy CM. Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2016. [cited 2019 Dec 16]. Available from: http://escholarship.umassmed.edu/gsbs_diss/844.

Council of Science Editors:

Duffy CM. Structural Mechanisms of the Sliding Clamp and Sliding Clamp Loader: Insights into Disease and Function: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2016. Available from: http://escholarship.umassmed.edu/gsbs_diss/844


University of California – Riverside

23. Chen, Zhijie. Illuminating Biology With Engineered Fluorescent Proteins.

Degree: Chemistry, 2016, University of California – Riverside

 Fluorescent proteins (FPs) emerged in the mid-90s as a powerful tool for life science research. Among its numerous applications, FPs is best known as reporter… (more)

Subjects/Keywords: Chemistry; Biochemistry; Biology; Fluorescent Proteins; Genetically Encoded Fluorescent Probes; Hydrogen Sulfide; Peroxynitrite; Unnatural Amino Acids; Zinc Ion

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APA (6th Edition):

Chen, Z. (2016). Illuminating Biology With Engineered Fluorescent Proteins. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/3zp2n2zt

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):

Chen, Zhijie. “Illuminating Biology With Engineered Fluorescent Proteins.” 2016. Thesis, University of California – Riverside. Accessed December 16, 2019. http://www.escholarship.org/uc/item/3zp2n2zt.

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

MLA Handbook (7th Edition):

Chen, Zhijie. “Illuminating Biology With Engineered Fluorescent Proteins.” 2016. Web. 16 Dec 2019.

Vancouver:

Chen Z. Illuminating Biology With Engineered Fluorescent Proteins. [Internet] [Thesis]. University of California – Riverside; 2016. [cited 2019 Dec 16]. Available from: http://www.escholarship.org/uc/item/3zp2n2zt.

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

Council of Science Editors:

Chen Z. Illuminating Biology With Engineered Fluorescent Proteins. [Thesis]. University of California – Riverside; 2016. Available from: http://www.escholarship.org/uc/item/3zp2n2zt

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


Iowa State University

24. Young, Isaac. Introducing multiple sites of acetylation to histone H3 via nonsense suppression.

Degree: 2016, Iowa State University

 A common post-translational modification (PTM) of proteins is lysine acetylation. This is an especially ubiquitous PTM in the histones of chromatin, and is important for… (more)

Subjects/Keywords: acetylation; chromatin; Nonsense suppression; Nucleosome stability; SAGA (Spt-ada-gcn5 acetyltransferase); unnatural amino acid; Biochemistry; Biophysics; Molecular Biology

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APA (6th Edition):

Young, I. (2016). Introducing multiple sites of acetylation to histone H3 via nonsense suppression. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/15850

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):

Young, Isaac. “Introducing multiple sites of acetylation to histone H3 via nonsense suppression.” 2016. Thesis, Iowa State University. Accessed December 16, 2019. https://lib.dr.iastate.edu/etd/15850.

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

MLA Handbook (7th Edition):

Young, Isaac. “Introducing multiple sites of acetylation to histone H3 via nonsense suppression.” 2016. Web. 16 Dec 2019.

Vancouver:

Young I. Introducing multiple sites of acetylation to histone H3 via nonsense suppression. [Internet] [Thesis]. Iowa State University; 2016. [cited 2019 Dec 16]. Available from: https://lib.dr.iastate.edu/etd/15850.

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

Council of Science Editors:

Young I. Introducing multiple sites of acetylation to histone H3 via nonsense suppression. [Thesis]. Iowa State University; 2016. Available from: https://lib.dr.iastate.edu/etd/15850

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


Florida International University

25. Fang, Nan. Extraction, Purification and partial Characterization of a Carotenoid Binding Protein (CBP) from the Epidermis of the Monarch Butterfly Larvae (Danaus plexippus).

Degree: PhD, Chemistry, 2016, Florida International University

  This dissertation describes the purification and partial characterization of CBP from the epidermis of the monarch butterfly larvae (Danaus plexippus). A yellow protein-carotenoid complex… (more)

Subjects/Keywords: Carotenoid; carotenoid binding protein; lutein; fluorescence; surface plasmon resonance; Amino Acids, Peptides, and Proteins; Biochemistry; Carbohydrates; Equipment and Supplies

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APA (6th Edition):

Fang, N. (2016). Extraction, Purification and partial Characterization of a Carotenoid Binding Protein (CBP) from the Epidermis of the Monarch Butterfly Larvae (Danaus plexippus). (Doctoral Dissertation). Florida International University. Retrieved from http://digitalcommons.fiu.edu/etd/2600 ; 10.25148/etd.FIDC000724 ; FIDC000724

Chicago Manual of Style (16th Edition):

Fang, Nan. “Extraction, Purification and partial Characterization of a Carotenoid Binding Protein (CBP) from the Epidermis of the Monarch Butterfly Larvae (Danaus plexippus).” 2016. Doctoral Dissertation, Florida International University. Accessed December 16, 2019. http://digitalcommons.fiu.edu/etd/2600 ; 10.25148/etd.FIDC000724 ; FIDC000724.

MLA Handbook (7th Edition):

Fang, Nan. “Extraction, Purification and partial Characterization of a Carotenoid Binding Protein (CBP) from the Epidermis of the Monarch Butterfly Larvae (Danaus plexippus).” 2016. Web. 16 Dec 2019.

Vancouver:

Fang N. Extraction, Purification and partial Characterization of a Carotenoid Binding Protein (CBP) from the Epidermis of the Monarch Butterfly Larvae (Danaus plexippus). [Internet] [Doctoral dissertation]. Florida International University; 2016. [cited 2019 Dec 16]. Available from: http://digitalcommons.fiu.edu/etd/2600 ; 10.25148/etd.FIDC000724 ; FIDC000724.

Council of Science Editors:

Fang N. Extraction, Purification and partial Characterization of a Carotenoid Binding Protein (CBP) from the Epidermis of the Monarch Butterfly Larvae (Danaus plexippus). [Doctoral Dissertation]. Florida International University; 2016. Available from: http://digitalcommons.fiu.edu/etd/2600 ; 10.25148/etd.FIDC000724 ; FIDC000724


University of Louisville

26. Faughn, Jon David. The N-terminal methyltransferase homologs NRMT1 and NRMT2 exhibit novel regulation of activity through heterotrimer formation.

Degree: PhD, 2018, University of Louisville

  Protein, DNA, and RNA methyltransferases have an ever-expanding list of novel substrates and catalytic activities. Even within families and between homologs, it is becoming… (more)

Subjects/Keywords: protein; methylation; enzyme; epigenetic; regulation; structural; Amino Acids, Peptides, and Proteins; Biochemistry; Enzymes and Coenzymes; Molecular Biology; Molecular Genetics; Structural Biology

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APA (6th Edition):

Faughn, J. D. (2018). The N-terminal methyltransferase homologs NRMT1 and NRMT2 exhibit novel regulation of activity through heterotrimer formation. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/3012 ; https://ir.library.louisville.edu/etd/3012

Chicago Manual of Style (16th Edition):

Faughn, Jon David. “The N-terminal methyltransferase homologs NRMT1 and NRMT2 exhibit novel regulation of activity through heterotrimer formation.” 2018. Doctoral Dissertation, University of Louisville. Accessed December 16, 2019. 10.18297/etd/3012 ; https://ir.library.louisville.edu/etd/3012.

MLA Handbook (7th Edition):

Faughn, Jon David. “The N-terminal methyltransferase homologs NRMT1 and NRMT2 exhibit novel regulation of activity through heterotrimer formation.” 2018. Web. 16 Dec 2019.

Vancouver:

Faughn JD. The N-terminal methyltransferase homologs NRMT1 and NRMT2 exhibit novel regulation of activity through heterotrimer formation. [Internet] [Doctoral dissertation]. University of Louisville; 2018. [cited 2019 Dec 16]. Available from: 10.18297/etd/3012 ; https://ir.library.louisville.edu/etd/3012.

Council of Science Editors:

Faughn JD. The N-terminal methyltransferase homologs NRMT1 and NRMT2 exhibit novel regulation of activity through heterotrimer formation. [Doctoral Dissertation]. University of Louisville; 2018. Available from: 10.18297/etd/3012 ; https://ir.library.louisville.edu/etd/3012


Columbia University

27. Anzalone, Andrew Vito. Reprogramming protein synthesis for cell engineering.

Degree: 2015, Columbia University

 Synthetic biology, which aims to enable the design and assembly of customized biological systems, holds great promise for delivering solutions to numerous modern day challenges… (more)

Subjects/Keywords: Proteins – Synthesis; Bioengineering; Amino acids – Biotechnology; RNA-protein interactions; Synthetic biology; Biochemistry; Chemistry, Organic; Biology; Molecular biology

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

APA (6th Edition):

Anzalone, A. V. (2015). Reprogramming protein synthesis for cell engineering. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8416WTD

Chicago Manual of Style (16th Edition):

Anzalone, Andrew Vito. “Reprogramming protein synthesis for cell engineering.” 2015. Doctoral Dissertation, Columbia University. Accessed December 16, 2019. https://doi.org/10.7916/D8416WTD.

MLA Handbook (7th Edition):

Anzalone, Andrew Vito. “Reprogramming protein synthesis for cell engineering.” 2015. Web. 16 Dec 2019.

Vancouver:

Anzalone AV. Reprogramming protein synthesis for cell engineering. [Internet] [Doctoral dissertation]. Columbia University; 2015. [cited 2019 Dec 16]. Available from: https://doi.org/10.7916/D8416WTD.

Council of Science Editors:

Anzalone AV. Reprogramming protein synthesis for cell engineering. [Doctoral Dissertation]. Columbia University; 2015. Available from: https://doi.org/10.7916/D8416WTD


University of Iowa

28. Miller, Mark Stephen. Use of osmotic coefficient measurements to validate and to correct the interaction thermodynamics of amino acids in molecular dynamics simulations.

Degree: PhD, Biochemistry, 2018, University of Iowa

  Molecular dynamics simulations are an increasingly valuable tool to biochemical researchers: advances in computational power have expanded the range of biomolecules that can be… (more)

Subjects/Keywords: Amino Acid Interactions; Force Field Validation and Optimization; Molecular Dynamics Simulations; Osmotic Coefficient and Osmotic Pressure; Biochemistry

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

APA (6th Edition):

Miller, M. S. (2018). Use of osmotic coefficient measurements to validate and to correct the interaction thermodynamics of amino acids in molecular dynamics simulations. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6476

Chicago Manual of Style (16th Edition):

Miller, Mark Stephen. “Use of osmotic coefficient measurements to validate and to correct the interaction thermodynamics of amino acids in molecular dynamics simulations.” 2018. Doctoral Dissertation, University of Iowa. Accessed December 16, 2019. https://ir.uiowa.edu/etd/6476.

MLA Handbook (7th Edition):

Miller, Mark Stephen. “Use of osmotic coefficient measurements to validate and to correct the interaction thermodynamics of amino acids in molecular dynamics simulations.” 2018. Web. 16 Dec 2019.

Vancouver:

Miller MS. Use of osmotic coefficient measurements to validate and to correct the interaction thermodynamics of amino acids in molecular dynamics simulations. [Internet] [Doctoral dissertation]. University of Iowa; 2018. [cited 2019 Dec 16]. Available from: https://ir.uiowa.edu/etd/6476.

Council of Science Editors:

Miller MS. Use of osmotic coefficient measurements to validate and to correct the interaction thermodynamics of amino acids in molecular dynamics simulations. [Doctoral Dissertation]. University of Iowa; 2018. Available from: https://ir.uiowa.edu/etd/6476


University of Kansas

29. Bommana, Rupesh. Degradation of therapeutic proteins: Screening methods and identification of epimerized amino acids and local conformational changes in light exposed proteins.

Degree: PhD, Pharmaceutical Chemistry, 2017, University of Kansas

 Protein-based pharmaceuticals are a fast growing class of therapeutics, which are widely used in the treatment of various diseases such as cancers and autoimmune diseases.… (more)

Subjects/Keywords: Pharmaceutical sciences; Chemistry; Biochemistry; amino acid analysis; fluorogenic derivatization; hydrogen deuterium exchange mass spectrometry; light exposure; monoclonal antibody; protein degradation

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

APA (6th Edition):

Bommana, R. (2017). Degradation of therapeutic proteins: Screening methods and identification of epimerized amino acids and local conformational changes in light exposed proteins. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27834

Chicago Manual of Style (16th Edition):

Bommana, Rupesh. “Degradation of therapeutic proteins: Screening methods and identification of epimerized amino acids and local conformational changes in light exposed proteins.” 2017. Doctoral Dissertation, University of Kansas. Accessed December 16, 2019. http://hdl.handle.net/1808/27834.

MLA Handbook (7th Edition):

Bommana, Rupesh. “Degradation of therapeutic proteins: Screening methods and identification of epimerized amino acids and local conformational changes in light exposed proteins.” 2017. Web. 16 Dec 2019.

Vancouver:

Bommana R. Degradation of therapeutic proteins: Screening methods and identification of epimerized amino acids and local conformational changes in light exposed proteins. [Internet] [Doctoral dissertation]. University of Kansas; 2017. [cited 2019 Dec 16]. Available from: http://hdl.handle.net/1808/27834.

Council of Science Editors:

Bommana R. Degradation of therapeutic proteins: Screening methods and identification of epimerized amino acids and local conformational changes in light exposed proteins. [Doctoral Dissertation]. University of Kansas; 2017. Available from: http://hdl.handle.net/1808/27834


Wilfrid Laurier University

30. Rice, Kyle. Characterization of the Microbial Phosphonate-Activating PntC Enzymes.

Degree: 2019, Wilfrid Laurier University

 New strategies are urgently needed to combat infectious diseases in an era of rising antibiotic resistance. Furthermore, an emerging appreciation for the human microbiome’s role… (more)

Subjects/Keywords: Nucleotidyltransferase; Enzyme Kinetics; Proteins; Amino Acids, Peptides, and Proteins; Biochemistry; Enzymes and Coenzymes; Nucleic Acids, Nucleotides, and Nucleosides; Other Chemistry

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

APA (6th Edition):

Rice, K. (2019). Characterization of the Microbial Phosphonate-Activating PntC Enzymes. (Thesis). Wilfrid Laurier University. Retrieved from https://scholars.wlu.ca/etd/2163

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):

Rice, Kyle. “Characterization of the Microbial Phosphonate-Activating PntC Enzymes.” 2019. Thesis, Wilfrid Laurier University. Accessed December 16, 2019. https://scholars.wlu.ca/etd/2163.

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

MLA Handbook (7th Edition):

Rice, Kyle. “Characterization of the Microbial Phosphonate-Activating PntC Enzymes.” 2019. Web. 16 Dec 2019.

Vancouver:

Rice K. Characterization of the Microbial Phosphonate-Activating PntC Enzymes. [Internet] [Thesis]. Wilfrid Laurier University; 2019. [cited 2019 Dec 16]. Available from: https://scholars.wlu.ca/etd/2163.

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

Council of Science Editors:

Rice K. Characterization of the Microbial Phosphonate-Activating PntC Enzymes. [Thesis]. Wilfrid Laurier University; 2019. Available from: https://scholars.wlu.ca/etd/2163

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

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