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Dept: Chemistry and Biochemistry

You searched for subject:(Ligand binding Biochemistry ). Showing records 1 – 30 of 389 total matches.

[1] [2] [3] [4] [5] … [13]

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Georgia Tech

1. Watt, Terry J. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.

Degree: PhD, Chemistry and Biochemistry, 2007, Georgia Tech

 The human retinoid X receptor alpha (hRXRalpha) is a member of the nuclear receptor super-family of ligand-activated transcription factors. The Doyle laboratory has previously engineered… (more)

Subjects/Keywords: Ligand binding; Protein engineering; Oligomerization; Thermal denaturation; Retinoid X receptor; Retinoids; Nuclear receptors (Biochemistry); Ligand binding (Biochemistry); DNA

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APA (6th Edition):

Watt, T. J. (2007). Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26647

Chicago Manual of Style (16th Edition):

Watt, Terry J. “Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.” 2007. Doctoral Dissertation, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/26647.

MLA Handbook (7th Edition):

Watt, Terry J. “Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants.” 2007. Web. 28 Feb 2020.

Vancouver:

Watt TJ. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/26647.

Council of Science Editors:

Watt TJ. Engineering a better receptor: characterization of retinoid x receptor alpha and functional variants. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/26647

2. Duraj-Thatte, Anna. Fluorescent GFP chromophores as potential ligands for various nuclear receptors.

Degree: PhD, Chemistry and Biochemistry, 2012, Georgia Tech

 Nuclear receptors are ligand activated transcription factors, where upon binding with small molecule ligands, these proteins are involved in the regulation of gene expression. To… (more)

Subjects/Keywords: GFPchromophore; Ligand; Fluorescent ligand; Nuclear receptor; Green fluorescent protein; Ligand binding (Biochemistry); Ligands (Biochemistry)

…Structure of DNA binding domain. 5 Figure 1.3: Structure of the ligand binding domain. 7… …Figure 1.4: Ligand binding induces conformational change of the LBD of nuclear receptor. 9… …with estradiol. 37 Figure 3.3: ERα ligand binding pocket. 38 Figure 3.4: The structures… …Ligand binding domain LBP Ligand bind pocket LRH-1 Liver receptor homolog-1 -LW Minus… …SUMMARY Nuclear receptors are ligand-activated transcription factors, where upon binding with… 

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APA (6th Edition):

Duraj-Thatte, A. (2012). Fluorescent GFP chromophores as potential ligands for various nuclear receptors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/44764

Chicago Manual of Style (16th Edition):

Duraj-Thatte, Anna. “Fluorescent GFP chromophores as potential ligands for various nuclear receptors.” 2012. Doctoral Dissertation, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/44764.

MLA Handbook (7th Edition):

Duraj-Thatte, Anna. “Fluorescent GFP chromophores as potential ligands for various nuclear receptors.” 2012. Web. 28 Feb 2020.

Vancouver:

Duraj-Thatte A. Fluorescent GFP chromophores as potential ligands for various nuclear receptors. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/44764.

Council of Science Editors:

Duraj-Thatte A. Fluorescent GFP chromophores as potential ligands for various nuclear receptors. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/44764


Georgia Tech

3. Enekwa, C. Denise. In silico design of novel binding ligands for biological targets.

Degree: MS, Chemistry and Biochemistry, 2010, Georgia Tech

 An in silico design algorithm has been developed to design binding ligands for protein targets of known three-dimensional structure. In this method, the binding energy… (more)

Subjects/Keywords: De novo binding; In silico design; Protein docking; Computer simulation; Ligand binding (Biochemistry); Protein engineering

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APA (6th Edition):

Enekwa, C. D. (2010). In silico design of novel binding ligands for biological targets. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/41067

Chicago Manual of Style (16th Edition):

Enekwa, C Denise. “In silico design of novel binding ligands for biological targets.” 2010. Masters Thesis, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/41067.

MLA Handbook (7th Edition):

Enekwa, C Denise. “In silico design of novel binding ligands for biological targets.” 2010. Web. 28 Feb 2020.

Vancouver:

Enekwa CD. In silico design of novel binding ligands for biological targets. [Internet] [Masters thesis]. Georgia Tech; 2010. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/41067.

Council of Science Editors:

Enekwa CD. In silico design of novel binding ligands for biological targets. [Masters Thesis]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/41067

4. Ousley, Amanda. Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 The human vitamin D receptor (hVDR) is a member of the nuclear receptor superfamily, involved in calcium and phosphate homeostasis; hence implicated in a number… (more)

Subjects/Keywords: Lithocholic acid; Cholecalciferol; Human vitamin D receptor; Nuclear receptors; Vitamin D in the body; Protein engineering; Ligand binding (Biochemistry); Receptor complexes (Biochemistry); Mutagenesis

…References 111 CHAPTER 5 HVDR LIGAND BINDING STUDIES 113 5.1 Introduction 113 5.2 Expression… …and Purification of Proteins 113 5.2.1 Cloning VDR Ligand Binding Domains into a Bacterial… …Structure 14 Figure 2.1: Known Important Residues in the hVDR Ligand Binding Pocket 26 Figure… …Ligand Binding Domain LBP Ligand Binding Pocket LCA Lithocholic Acid MBP Maltose Binding… …the ligand binding pocket in comparison to the docked analysis of cholecalciferol with wild… 

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APA (6th Edition):

Ousley, A. (2011). Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39580

Chicago Manual of Style (16th Edition):

Ousley, Amanda. “Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands.” 2011. Doctoral Dissertation, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/39580.

MLA Handbook (7th Edition):

Ousley, Amanda. “Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands.” 2011. Web. 28 Feb 2020.

Vancouver:

Ousley A. Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/39580.

Council of Science Editors:

Ousley A. Engineering the human vitamin D receptor to bind a novel small molecule: investigating the structure-function relationship between human vitamin d receptor and various ligands. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/39580


Utah State University

5. Bakelar, Jeremy W. Binding Interactions of (R)- and (S)-hydroxypropyl-CoM Dehydrogenases and the Zinc Knuckle Proteins Air1 and Air2.

Degree: PhD, Chemistry and Biochemistry, 2015, Utah State University

  This work is focused on understanding protein function by describing how paralogous proteins with overlapping and distinct functions interact with their substrates and with… (more)

Subjects/Keywords: Binding; interactions; Hydroxypropyl-CoM; Dehydrogenases; zinc; knuckle; proteins; air1; air2; Biochemistry

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APA (6th Edition):

Bakelar, J. W. (2015). Binding Interactions of (R)- and (S)-hydroxypropyl-CoM Dehydrogenases and the Zinc Knuckle Proteins Air1 and Air2. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/4273

Chicago Manual of Style (16th Edition):

Bakelar, Jeremy W. “Binding Interactions of (R)- and (S)-hydroxypropyl-CoM Dehydrogenases and the Zinc Knuckle Proteins Air1 and Air2.” 2015. Doctoral Dissertation, Utah State University. Accessed February 28, 2020. https://digitalcommons.usu.edu/etd/4273.

MLA Handbook (7th Edition):

Bakelar, Jeremy W. “Binding Interactions of (R)- and (S)-hydroxypropyl-CoM Dehydrogenases and the Zinc Knuckle Proteins Air1 and Air2.” 2015. Web. 28 Feb 2020.

Vancouver:

Bakelar JW. Binding Interactions of (R)- and (S)-hydroxypropyl-CoM Dehydrogenases and the Zinc Knuckle Proteins Air1 and Air2. [Internet] [Doctoral dissertation]. Utah State University; 2015. [cited 2020 Feb 28]. Available from: https://digitalcommons.usu.edu/etd/4273.

Council of Science Editors:

Bakelar JW. Binding Interactions of (R)- and (S)-hydroxypropyl-CoM Dehydrogenases and the Zinc Knuckle Proteins Air1 and Air2. [Doctoral Dissertation]. Utah State University; 2015. Available from: https://digitalcommons.usu.edu/etd/4273

6. Engelhart, Aaron Edward. Nucleic acid assembly, polymerization, and ligand binding.

Degree: PhD, Chemistry and Biochemistry, 2012, Georgia Tech

 In the past 30 years, the discovery of capabilities of nucleic acids far beyond their well-known information-bearing capacity has profoundly influenced our understanding of these… (more)

Subjects/Keywords: Polymer; Cyclization; Dynamic covalent chemistry; Origin of life; RNA world; Reversible covalent bond; Template directed synthesis; Supramolecular chemistry; Chemistry, Physical and theoretical; Nucleic acids; Molecules; Ligand binding (Biochemistry)

…towards such a synthetic route. In these systems, a nucleic-acid binding ligand drives the… …contemporary life. In Chapter 2, I demonstrate how a nucleic-acid binding ligand can 5 drive the… …demonstrate the utility of ligand binding in assembling a novel backbone containing a reversible… …Chapters 4 and 5, I report the binding of a novel nucleic acid ligand to a G-quadruplex nucleic… …viii LIST OF TABLES Page Table 3.1: Template and ligand dependence of yields of morpholine… 

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APA (6th Edition):

Engelhart, A. E. (2012). Nucleic acid assembly, polymerization, and ligand binding. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45979

Chicago Manual of Style (16th Edition):

Engelhart, Aaron Edward. “Nucleic acid assembly, polymerization, and ligand binding.” 2012. Doctoral Dissertation, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/45979.

MLA Handbook (7th Edition):

Engelhart, Aaron Edward. “Nucleic acid assembly, polymerization, and ligand binding.” 2012. Web. 28 Feb 2020.

Vancouver:

Engelhart AE. Nucleic acid assembly, polymerization, and ligand binding. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/45979.

Council of Science Editors:

Engelhart AE. Nucleic acid assembly, polymerization, and ligand binding. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/45979


Seton Hall University

7. Elshaer, Mohammed R. Porphyrin Cross-Linkers for Generating Soluble Molecularly Imprinted Polymers from Polyethyleneimine.

Degree: PhD, Chemistry and Biochemistry, 2014, Seton Hall University

  Molecular recognition is vital to many biochemical processes and is at the heart of promising bio-medically related technologies. Molecular imprinting has a long-standing history… (more)

Subjects/Keywords: Quadruplex DNA; Synthesis of Cationic Porphyrins; DNA Binding; EDC Coupling Reactions; DNA Binding Polymers; Quadruplex Binding Ligands; Biochemistry; Biotechnology; Materials Chemistry; Organic Chemistry; Polymer Chemistry

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APA (6th Edition):

Elshaer, M. R. (2014). Porphyrin Cross-Linkers for Generating Soluble Molecularly Imprinted Polymers from Polyethyleneimine. (Doctoral Dissertation). Seton Hall University. Retrieved from http://scholarship.shu.edu/dissertations/1948

Chicago Manual of Style (16th Edition):

Elshaer, Mohammed R. “Porphyrin Cross-Linkers for Generating Soluble Molecularly Imprinted Polymers from Polyethyleneimine.” 2014. Doctoral Dissertation, Seton Hall University. Accessed February 28, 2020. http://scholarship.shu.edu/dissertations/1948.

MLA Handbook (7th Edition):

Elshaer, Mohammed R. “Porphyrin Cross-Linkers for Generating Soluble Molecularly Imprinted Polymers from Polyethyleneimine.” 2014. Web. 28 Feb 2020.

Vancouver:

Elshaer MR. Porphyrin Cross-Linkers for Generating Soluble Molecularly Imprinted Polymers from Polyethyleneimine. [Internet] [Doctoral dissertation]. Seton Hall University; 2014. [cited 2020 Feb 28]. Available from: http://scholarship.shu.edu/dissertations/1948.

Council of Science Editors:

Elshaer MR. Porphyrin Cross-Linkers for Generating Soluble Molecularly Imprinted Polymers from Polyethyleneimine. [Doctoral Dissertation]. Seton Hall University; 2014. Available from: http://scholarship.shu.edu/dissertations/1948

8. Connell, George Raymond. Electroimmunoassay a New Competitive Protein Binding Assay Using Antibody Selective Electrodes.

Degree: MS, Chemistry and Biochemistry, 1982, Old Dominion University

  The purpose of this study was to utilize concept of antibody selective electrodes to develop a new competitive protein binding assay. This is a… (more)

Subjects/Keywords: Electrodes; Proteins; Binding assay; RIA; Biochemistry

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APA (6th Edition):

Connell, G. R. (1982). Electroimmunoassay a New Competitive Protein Binding Assay Using Antibody Selective Electrodes. (Thesis). Old Dominion University. Retrieved from https://digitalcommons.odu.edu/chemistry_etds/47

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):

Connell, George Raymond. “Electroimmunoassay a New Competitive Protein Binding Assay Using Antibody Selective Electrodes.” 1982. Thesis, Old Dominion University. Accessed February 28, 2020. https://digitalcommons.odu.edu/chemistry_etds/47.

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

MLA Handbook (7th Edition):

Connell, George Raymond. “Electroimmunoassay a New Competitive Protein Binding Assay Using Antibody Selective Electrodes.” 1982. Web. 28 Feb 2020.

Vancouver:

Connell GR. Electroimmunoassay a New Competitive Protein Binding Assay Using Antibody Selective Electrodes. [Internet] [Thesis]. Old Dominion University; 1982. [cited 2020 Feb 28]. Available from: https://digitalcommons.odu.edu/chemistry_etds/47.

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

Council of Science Editors:

Connell GR. Electroimmunoassay a New Competitive Protein Binding Assay Using Antibody Selective Electrodes. [Thesis]. Old Dominion University; 1982. Available from: https://digitalcommons.odu.edu/chemistry_etds/47

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

9. Osa-Andrews, Bremansu. Engineering of Two-Color ATP-Binding Cassette Biosensor Proteins for Discovery of Novel Substrates and Modulators.

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

  ATP-binding cassette (ABC) transporter proteins are a vast, ubiquitous superfamily of proteins most of which unlock the energy from ATP-binding and hydrolysis to influx… (more)

Subjects/Keywords: ATP-binding cassette proteins; Biosensors; Fluorescence resonance energy transfer; Multidrug resistance; P-glycoprotein; Two-color MRP1; Biochemistry

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APA (6th Edition):

Osa-Andrews, B. (2018). Engineering of Two-Color ATP-Binding Cassette Biosensor Proteins for Discovery of Novel Substrates and Modulators. (Doctoral Dissertation). South Dakota State University. Retrieved from https://openprairie.sdstate.edu/etd/2955

Chicago Manual of Style (16th Edition):

Osa-Andrews, Bremansu. “Engineering of Two-Color ATP-Binding Cassette Biosensor Proteins for Discovery of Novel Substrates and Modulators.” 2018. Doctoral Dissertation, South Dakota State University. Accessed February 28, 2020. https://openprairie.sdstate.edu/etd/2955.

MLA Handbook (7th Edition):

Osa-Andrews, Bremansu. “Engineering of Two-Color ATP-Binding Cassette Biosensor Proteins for Discovery of Novel Substrates and Modulators.” 2018. Web. 28 Feb 2020.

Vancouver:

Osa-Andrews B. Engineering of Two-Color ATP-Binding Cassette Biosensor Proteins for Discovery of Novel Substrates and Modulators. [Internet] [Doctoral dissertation]. South Dakota State University; 2018. [cited 2020 Feb 28]. Available from: https://openprairie.sdstate.edu/etd/2955.

Council of Science Editors:

Osa-Andrews B. Engineering of Two-Color ATP-Binding Cassette Biosensor Proteins for Discovery of Novel Substrates and Modulators. [Doctoral Dissertation]. South Dakota State University; 2018. Available from: https://openprairie.sdstate.edu/etd/2955


Utah State University

10. Chen, Michael J. Characterization of an Axial Ligand Substitution in Sperm Whale Myoglobin.

Degree: MS, Chemistry and Biochemistry, 1995, Utah State University

  Of central importance to the study of heme proteins are the effects imposed by axial ligand(s) on the heme structure and, therefore, on the… (more)

Subjects/Keywords: Axial Ligand; Sperm Whale; Myoglobin; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

Chen, M. J. (1995). Characterization of an Axial Ligand Substitution in Sperm Whale Myoglobin. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/7189

Chicago Manual of Style (16th Edition):

Chen, Michael J. “Characterization of an Axial Ligand Substitution in Sperm Whale Myoglobin.” 1995. Masters Thesis, Utah State University. Accessed February 28, 2020. https://digitalcommons.usu.edu/etd/7189.

MLA Handbook (7th Edition):

Chen, Michael J. “Characterization of an Axial Ligand Substitution in Sperm Whale Myoglobin.” 1995. Web. 28 Feb 2020.

Vancouver:

Chen MJ. Characterization of an Axial Ligand Substitution in Sperm Whale Myoglobin. [Internet] [Masters thesis]. Utah State University; 1995. [cited 2020 Feb 28]. Available from: https://digitalcommons.usu.edu/etd/7189.

Council of Science Editors:

Chen MJ. Characterization of an Axial Ligand Substitution in Sperm Whale Myoglobin. [Masters Thesis]. Utah State University; 1995. Available from: https://digitalcommons.usu.edu/etd/7189


Utah State University

11. Wilson, Emily. Photoaffinity Labeling of the Antimycin Binding Site in Rhodopseudomonas sphaeroides.

Degree: MS, Chemistry and Biochemistry, 1984, Utah State University

  The purpose of this study was to identify the site of interaction of antimycin with the ubiquinone-cytochrome b-c1 oxidoreductase in the photosynthetic bacteria, Rhodopseudomonas… (more)

Subjects/Keywords: photoaffinity; antimycin; binding; rhodopseudomonas sphaeroides; Biochemistry, Biophysics, and Structural Biology; Chemistry

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APA (6th Edition):

Wilson, E. (1984). Photoaffinity Labeling of the Antimycin Binding Site in Rhodopseudomonas sphaeroides. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/7185

Chicago Manual of Style (16th Edition):

Wilson, Emily. “Photoaffinity Labeling of the Antimycin Binding Site in Rhodopseudomonas sphaeroides.” 1984. Masters Thesis, Utah State University. Accessed February 28, 2020. https://digitalcommons.usu.edu/etd/7185.

MLA Handbook (7th Edition):

Wilson, Emily. “Photoaffinity Labeling of the Antimycin Binding Site in Rhodopseudomonas sphaeroides.” 1984. Web. 28 Feb 2020.

Vancouver:

Wilson E. Photoaffinity Labeling of the Antimycin Binding Site in Rhodopseudomonas sphaeroides. [Internet] [Masters thesis]. Utah State University; 1984. [cited 2020 Feb 28]. Available from: https://digitalcommons.usu.edu/etd/7185.

Council of Science Editors:

Wilson E. Photoaffinity Labeling of the Antimycin Binding Site in Rhodopseudomonas sphaeroides. [Masters Thesis]. Utah State University; 1984. Available from: https://digitalcommons.usu.edu/etd/7185


University of Notre Dame

12. Monica M. Schroll. Analysis of Nutrient Based Intervention for Colorectal Cancer Treatment Using Mass Spectrometry</h1>.

Degree: PhD, Chemistry and Biochemistry, 2018, University of Notre Dame

  Colorectal cancer is the third most common cancer worldwide, in the past several decades the incidence of colorectal cancer has decreased, yet the overall… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Schroll, M. M. (2018). Analysis of Nutrient Based Intervention for Colorectal Cancer Treatment Using Mass Spectrometry</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/xs55m904014

Chicago Manual of Style (16th Edition):

Schroll, Monica M.. “Analysis of Nutrient Based Intervention for Colorectal Cancer Treatment Using Mass Spectrometry</h1>.” 2018. Doctoral Dissertation, University of Notre Dame. Accessed February 28, 2020. https://curate.nd.edu/show/xs55m904014.

MLA Handbook (7th Edition):

Schroll, Monica M.. “Analysis of Nutrient Based Intervention for Colorectal Cancer Treatment Using Mass Spectrometry</h1>.” 2018. Web. 28 Feb 2020.

Vancouver:

Schroll MM. Analysis of Nutrient Based Intervention for Colorectal Cancer Treatment Using Mass Spectrometry</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2018. [cited 2020 Feb 28]. Available from: https://curate.nd.edu/show/xs55m904014.

Council of Science Editors:

Schroll MM. Analysis of Nutrient Based Intervention for Colorectal Cancer Treatment Using Mass Spectrometry</h1>. [Doctoral Dissertation]. University of Notre Dame; 2018. Available from: https://curate.nd.edu/show/xs55m904014


University of California – San Diego

13. Lumba, Charles Leonard Mallari. Splice Site Recognition During Early Spliceosome Assembly.

Degree: Chemistry and Biochemistry, 2019, University of California – San Diego

 Protein coding sequences in most eukaryotic pre-messenger RNAs (pre-mRNA) are interrupted by intervening sequences called introns, while the protein coding sequences are termed exons. The… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Lumba, C. L. M. (2019). Splice Site Recognition During Early Spliceosome Assembly. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/2t16n5t2

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):

Lumba, Charles Leonard Mallari. “Splice Site Recognition During Early Spliceosome Assembly.” 2019. Thesis, University of California – San Diego. Accessed February 28, 2020. http://www.escholarship.org/uc/item/2t16n5t2.

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

MLA Handbook (7th Edition):

Lumba, Charles Leonard Mallari. “Splice Site Recognition During Early Spliceosome Assembly.” 2019. Web. 28 Feb 2020.

Vancouver:

Lumba CLM. Splice Site Recognition During Early Spliceosome Assembly. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2020 Feb 28]. Available from: http://www.escholarship.org/uc/item/2t16n5t2.

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

Council of Science Editors:

Lumba CLM. Splice Site Recognition During Early Spliceosome Assembly. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/2t16n5t2

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


University of California – San Diego

14. Bracamontes, Gabriel. Investigating how Translation is Impacted, After Fermentative Growth, in S. cerevisiae.

Degree: Chemistry and Biochemistry, 2019, University of California – San Diego

 When yeast cells endure environmental changes, they respond transcriptionally and translationally causing a fluctuation of gene expression dependent on the environmental changes. Understanding how yeast… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Bracamontes, G. (2019). Investigating how Translation is Impacted, After Fermentative Growth, in S. cerevisiae. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/6784p8g2

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):

Bracamontes, Gabriel. “Investigating how Translation is Impacted, After Fermentative Growth, in S. cerevisiae.” 2019. Thesis, University of California – San Diego. Accessed February 28, 2020. http://www.escholarship.org/uc/item/6784p8g2.

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

MLA Handbook (7th Edition):

Bracamontes, Gabriel. “Investigating how Translation is Impacted, After Fermentative Growth, in S. cerevisiae.” 2019. Web. 28 Feb 2020.

Vancouver:

Bracamontes G. Investigating how Translation is Impacted, After Fermentative Growth, in S. cerevisiae. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2020 Feb 28]. Available from: http://www.escholarship.org/uc/item/6784p8g2.

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

Council of Science Editors:

Bracamontes G. Investigating how Translation is Impacted, After Fermentative Growth, in S. cerevisiae. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/6784p8g2

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


Florida State University

15. Miao, Yimin. Structure, Dynamics and Proton Conductance Mechanism of the M2 Protein Histidine Tetrad.

Degree: PhD, Chemistry and Biochemistry, 2015, Florida State University

Solid-state NMR takes advantage of studying membrane proteins in a native membrane-like lipid bilayer and has been used for generating exciting results. The magic angle… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Miao, Y. (2015). Structure, Dynamics and Proton Conductance Mechanism of the M2 Protein Histidine Tetrad. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-9407 ;

Chicago Manual of Style (16th Edition):

Miao, Yimin. “Structure, Dynamics and Proton Conductance Mechanism of the M2 Protein Histidine Tetrad.” 2015. Doctoral Dissertation, Florida State University. Accessed February 28, 2020. http://purl.flvc.org/fsu/fd/FSU_migr_etd-9407 ;.

MLA Handbook (7th Edition):

Miao, Yimin. “Structure, Dynamics and Proton Conductance Mechanism of the M2 Protein Histidine Tetrad.” 2015. Web. 28 Feb 2020.

Vancouver:

Miao Y. Structure, Dynamics and Proton Conductance Mechanism of the M2 Protein Histidine Tetrad. [Internet] [Doctoral dissertation]. Florida State University; 2015. [cited 2020 Feb 28]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9407 ;.

Council of Science Editors:

Miao Y. Structure, Dynamics and Proton Conductance Mechanism of the M2 Protein Histidine Tetrad. [Doctoral Dissertation]. Florida State University; 2015. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9407 ;


Florida State University

16. Kapur, Anshika. Peptide Mediated Delivery of Inorganic Nanomaterials.

Degree: PhD, Chemistry and Biochemistry, 2018, Florida State University

 The unique chemical, optical and physical properties of inorganic nanocrystals have generated tremendous interest to develop a variety of applications, most importantly as novel probes… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Kapur, A. (2018). Peptide Mediated Delivery of Inorganic Nanomaterials. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/2018_Su_Kapur_fsu_0071E_14514_comp ;

Chicago Manual of Style (16th Edition):

Kapur, Anshika. “Peptide Mediated Delivery of Inorganic Nanomaterials.” 2018. Doctoral Dissertation, Florida State University. Accessed February 28, 2020. http://purl.flvc.org/fsu/fd/2018_Su_Kapur_fsu_0071E_14514_comp ;.

MLA Handbook (7th Edition):

Kapur, Anshika. “Peptide Mediated Delivery of Inorganic Nanomaterials.” 2018. Web. 28 Feb 2020.

Vancouver:

Kapur A. Peptide Mediated Delivery of Inorganic Nanomaterials. [Internet] [Doctoral dissertation]. Florida State University; 2018. [cited 2020 Feb 28]. Available from: http://purl.flvc.org/fsu/fd/2018_Su_Kapur_fsu_0071E_14514_comp ;.

Council of Science Editors:

Kapur A. Peptide Mediated Delivery of Inorganic Nanomaterials. [Doctoral Dissertation]. Florida State University; 2018. Available from: http://purl.flvc.org/fsu/fd/2018_Su_Kapur_fsu_0071E_14514_comp ;


Florida State University

17. Martinez, Juliana Andrea. Studies on Human Glucokinase Regulation.

Degree: PhD, Chemistry and Biochemistry, 2016, Florida State University

 Over the last decades, the enzyme Glucokinase (GCK) has interested biochemists due to its physiological and kinetic characteristics. GCK is vital for glucose homeostasis, as… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Martinez, J. A. (2016). Studies on Human Glucokinase Regulation. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_FA2016_Martinez_fsu_0071E_13576 ;

Chicago Manual of Style (16th Edition):

Martinez, Juliana Andrea. “Studies on Human Glucokinase Regulation.” 2016. Doctoral Dissertation, Florida State University. Accessed February 28, 2020. http://purl.flvc.org/fsu/fd/FSU_FA2016_Martinez_fsu_0071E_13576 ;.

MLA Handbook (7th Edition):

Martinez, Juliana Andrea. “Studies on Human Glucokinase Regulation.” 2016. Web. 28 Feb 2020.

Vancouver:

Martinez JA. Studies on Human Glucokinase Regulation. [Internet] [Doctoral dissertation]. Florida State University; 2016. [cited 2020 Feb 28]. Available from: http://purl.flvc.org/fsu/fd/FSU_FA2016_Martinez_fsu_0071E_13576 ;.

Council of Science Editors:

Martinez JA. Studies on Human Glucokinase Regulation. [Doctoral Dissertation]. Florida State University; 2016. Available from: http://purl.flvc.org/fsu/fd/FSU_FA2016_Martinez_fsu_0071E_13576 ;


Florida State University

18. Bowler, Joseph M. Allosteric Activation of Human Glucokinase.

Degree: PhD, Chemistry and Biochemistry, 2014, Florida State University

 The hexokinase family of enzymes catalyzes the ATP-dependent phosphorylation of glucose to generate glucose 6-phosphate and ADP. Consistent with highly evolved catalysts, hexokinases I-III possess… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Bowler, J. M. (2014). Allosteric Activation of Human Glucokinase. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-9147 ;

Chicago Manual of Style (16th Edition):

Bowler, Joseph M. “Allosteric Activation of Human Glucokinase.” 2014. Doctoral Dissertation, Florida State University. Accessed February 28, 2020. http://purl.flvc.org/fsu/fd/FSU_migr_etd-9147 ;.

MLA Handbook (7th Edition):

Bowler, Joseph M. “Allosteric Activation of Human Glucokinase.” 2014. Web. 28 Feb 2020.

Vancouver:

Bowler JM. Allosteric Activation of Human Glucokinase. [Internet] [Doctoral dissertation]. Florida State University; 2014. [cited 2020 Feb 28]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9147 ;.

Council of Science Editors:

Bowler JM. Allosteric Activation of Human Glucokinase. [Doctoral Dissertation]. Florida State University; 2014. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9147 ;


Florida State University

19. Meng, Dan. Structure and Dynamics Study of Cu Transporting Atpase by NMR.

Degree: PhD, Chemistry and Biochemistry, 2014, Florida State University

 Copper transporting ATPase (Cu-ATPase) is a member of the P1B-subfamily of P-type ATPases, which catalyzes ATP-dependent copper delivery across cellular membranes. The energy derived from… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Meng, D. (2014). Structure and Dynamics Study of Cu Transporting Atpase by NMR. (Doctoral Dissertation). Florida State University. Retrieved from http://purl.flvc.org/fsu/fd/FSU_migr_etd-9217 ;

Chicago Manual of Style (16th Edition):

Meng, Dan. “Structure and Dynamics Study of Cu Transporting Atpase by NMR.” 2014. Doctoral Dissertation, Florida State University. Accessed February 28, 2020. http://purl.flvc.org/fsu/fd/FSU_migr_etd-9217 ;.

MLA Handbook (7th Edition):

Meng, Dan. “Structure and Dynamics Study of Cu Transporting Atpase by NMR.” 2014. Web. 28 Feb 2020.

Vancouver:

Meng D. Structure and Dynamics Study of Cu Transporting Atpase by NMR. [Internet] [Doctoral dissertation]. Florida State University; 2014. [cited 2020 Feb 28]. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9217 ;.

Council of Science Editors:

Meng D. Structure and Dynamics Study of Cu Transporting Atpase by NMR. [Doctoral Dissertation]. Florida State University; 2014. Available from: http://purl.flvc.org/fsu/fd/FSU_migr_etd-9217 ;


University of Windsor

20. Fochesato, Lee-Anne. Small Molecular Weight Modulators of Apoptosis and Senescence.

Degree: MA, Chemistry and Biochemistry, 2011, University of Windsor

 ABSTRACT Age-related neurodegenerative diseases are a major problem in industrialized nations, and affect millions of people worldwide. The pro-apoptotic protein Bax plays a crucial part… (more)

Subjects/Keywords: Biochemistry.

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APA (6th Edition):

Fochesato, L. (2011). Small Molecular Weight Modulators of Apoptosis and Senescence. (Masters Thesis). University of Windsor. Retrieved from https://scholar.uwindsor.ca/etd/70

Chicago Manual of Style (16th Edition):

Fochesato, Lee-Anne. “Small Molecular Weight Modulators of Apoptosis and Senescence.” 2011. Masters Thesis, University of Windsor. Accessed February 28, 2020. https://scholar.uwindsor.ca/etd/70.

MLA Handbook (7th Edition):

Fochesato, Lee-Anne. “Small Molecular Weight Modulators of Apoptosis and Senescence.” 2011. Web. 28 Feb 2020.

Vancouver:

Fochesato L. Small Molecular Weight Modulators of Apoptosis and Senescence. [Internet] [Masters thesis]. University of Windsor; 2011. [cited 2020 Feb 28]. Available from: https://scholar.uwindsor.ca/etd/70.

Council of Science Editors:

Fochesato L. Small Molecular Weight Modulators of Apoptosis and Senescence. [Masters Thesis]. University of Windsor; 2011. Available from: https://scholar.uwindsor.ca/etd/70


University of Windsor

21. Griffin, Carly. Evaluation of the Selective Anti-Cancer Activity of Natural and Synthetic Alkaloids.

Degree: PhD, Chemistry and Biochemistry, 2011, University of Windsor

 Cancer is a disease of uncontrolled cell growth and proliferation that is predicted to directly affect one-third of Canadians. Standard chemotherapy, which targets DNA or… (more)

Subjects/Keywords: Biochemistry.

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APA (6th Edition):

Griffin, C. (2011). Evaluation of the Selective Anti-Cancer Activity of Natural and Synthetic Alkaloids. (Doctoral Dissertation). University of Windsor. Retrieved from https://scholar.uwindsor.ca/etd/390

Chicago Manual of Style (16th Edition):

Griffin, Carly. “Evaluation of the Selective Anti-Cancer Activity of Natural and Synthetic Alkaloids.” 2011. Doctoral Dissertation, University of Windsor. Accessed February 28, 2020. https://scholar.uwindsor.ca/etd/390.

MLA Handbook (7th Edition):

Griffin, Carly. “Evaluation of the Selective Anti-Cancer Activity of Natural and Synthetic Alkaloids.” 2011. Web. 28 Feb 2020.

Vancouver:

Griffin C. Evaluation of the Selective Anti-Cancer Activity of Natural and Synthetic Alkaloids. [Internet] [Doctoral dissertation]. University of Windsor; 2011. [cited 2020 Feb 28]. Available from: https://scholar.uwindsor.ca/etd/390.

Council of Science Editors:

Griffin C. Evaluation of the Selective Anti-Cancer Activity of Natural and Synthetic Alkaloids. [Doctoral Dissertation]. University of Windsor; 2011. Available from: https://scholar.uwindsor.ca/etd/390


University of Windsor

22. Franklin, Norah. Regulation of MTMR2 by Phosphorylation: Subcellular Characterization and Functional Role in Vesicular Trafficking.

Degree: MA, Chemistry and Biochemistry, 2011, University of Windsor

 MTMR2 is an active member of the MTM family of inositol lipid phosphatases and the physiological substrates for MTMR2 play key roles in endosomal trafficking.… (more)

Subjects/Keywords: Biochemistry.

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APA (6th Edition):

Franklin, N. (2011). Regulation of MTMR2 by Phosphorylation: Subcellular Characterization and Functional Role in Vesicular Trafficking. (Masters Thesis). University of Windsor. Retrieved from https://scholar.uwindsor.ca/etd/71

Chicago Manual of Style (16th Edition):

Franklin, Norah. “Regulation of MTMR2 by Phosphorylation: Subcellular Characterization and Functional Role in Vesicular Trafficking.” 2011. Masters Thesis, University of Windsor. Accessed February 28, 2020. https://scholar.uwindsor.ca/etd/71.

MLA Handbook (7th Edition):

Franklin, Norah. “Regulation of MTMR2 by Phosphorylation: Subcellular Characterization and Functional Role in Vesicular Trafficking.” 2011. Web. 28 Feb 2020.

Vancouver:

Franklin N. Regulation of MTMR2 by Phosphorylation: Subcellular Characterization and Functional Role in Vesicular Trafficking. [Internet] [Masters thesis]. University of Windsor; 2011. [cited 2020 Feb 28]. Available from: https://scholar.uwindsor.ca/etd/71.

Council of Science Editors:

Franklin N. Regulation of MTMR2 by Phosphorylation: Subcellular Characterization and Functional Role in Vesicular Trafficking. [Masters Thesis]. University of Windsor; 2011. Available from: https://scholar.uwindsor.ca/etd/71


University of Windsor

23. Kaur, Harmanpreet. Development And Validation Of A Flow Device To Study Platelet Function In Vitro And Elucidating The Role Of Thymosin β 4 In Various Physiological Processes.

Degree: PhD, Chemistry and Biochemistry, 2011, University of Windsor

  Parallel plate flow chambers, simulating in vivo fluid shear stress, provide a real time insight into the dynamic process of platelet aggregation and investigation… (more)

Subjects/Keywords: Biochemistry.

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APA (6th Edition):

Kaur, H. (2011). Development And Validation Of A Flow Device To Study Platelet Function In Vitro And Elucidating The Role Of Thymosin β 4 In Various Physiological Processes. (Doctoral Dissertation). University of Windsor. Retrieved from https://scholar.uwindsor.ca/etd/393

Chicago Manual of Style (16th Edition):

Kaur, Harmanpreet. “Development And Validation Of A Flow Device To Study Platelet Function In Vitro And Elucidating The Role Of Thymosin β 4 In Various Physiological Processes.” 2011. Doctoral Dissertation, University of Windsor. Accessed February 28, 2020. https://scholar.uwindsor.ca/etd/393.

MLA Handbook (7th Edition):

Kaur, Harmanpreet. “Development And Validation Of A Flow Device To Study Platelet Function In Vitro And Elucidating The Role Of Thymosin β 4 In Various Physiological Processes.” 2011. Web. 28 Feb 2020.

Vancouver:

Kaur H. Development And Validation Of A Flow Device To Study Platelet Function In Vitro And Elucidating The Role Of Thymosin β 4 In Various Physiological Processes. [Internet] [Doctoral dissertation]. University of Windsor; 2011. [cited 2020 Feb 28]. Available from: https://scholar.uwindsor.ca/etd/393.

Council of Science Editors:

Kaur H. Development And Validation Of A Flow Device To Study Platelet Function In Vitro And Elucidating The Role Of Thymosin β 4 In Various Physiological Processes. [Doctoral Dissertation]. University of Windsor; 2011. Available from: https://scholar.uwindsor.ca/etd/393

24. Smith, Aubrey L. Facilitating multi-electron reactivity at low-coordinate cobalt complexes using redox-active ligands.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 In this study, we describe a detailed investigation of cobalt complexes containing redox-active ligands. We have prepared an electronic series of the complex in three… (more)

Subjects/Keywords: Coupling; Carbon-carbon; Redox-active ligand; Catalysis; Cobalt; Oxidation; Chemical reactions; Charge exchange; Ligands (Biochemistry)

…Instability of other complexes with tridentate phosphine ligand 146 5.4.4. Instability of other… …complexes containing bidentate phosphine ligand 147 5.4.5. Unstable complex with stabilizing… …tridentate nitrogen ligand 149 5.5. Conclusions 150 5.6. References 151 6. Future work and… …Cyclic voltammetry L Ligand ap2– Amidodphenolate isq1– Iminosemiquinonate ibq… …transfer CT Charge transfer LLCT Ligand-to-ligand charge transfer MLCT Metal-to-ligand… 

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APA (6th Edition):

Smith, A. L. (2011). Facilitating multi-electron reactivity at low-coordinate cobalt complexes using redox-active ligands. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/42745

Chicago Manual of Style (16th Edition):

Smith, Aubrey L. “Facilitating multi-electron reactivity at low-coordinate cobalt complexes using redox-active ligands.” 2011. Doctoral Dissertation, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/42745.

MLA Handbook (7th Edition):

Smith, Aubrey L. “Facilitating multi-electron reactivity at low-coordinate cobalt complexes using redox-active ligands.” 2011. Web. 28 Feb 2020.

Vancouver:

Smith AL. Facilitating multi-electron reactivity at low-coordinate cobalt complexes using redox-active ligands. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/42745.

Council of Science Editors:

Smith AL. Facilitating multi-electron reactivity at low-coordinate cobalt complexes using redox-active ligands. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/42745


University of Notre Dame

25. Patrick E. Rothstein. Nucleophilic Palladium Carbenes Utilizing Metal-Ligand Cooperativity Towards Small Molecule Activations</h1>.

Degree: PhD, Chemistry and Biochemistry, 2017, University of Notre Dame

  Transition-metal carbenes have long been known to exhibit unique reactivity and utilized in a wide variety of applications including synthetic methods for the production… (more)

Subjects/Keywords: metal ligand cooperativity; Inorganic Chemistry; Ligand Design; Small molecule activation

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APA (6th Edition):

Rothstein, P. E. (2017). Nucleophilic Palladium Carbenes Utilizing Metal-Ligand Cooperativity Towards Small Molecule Activations</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/vx021c21m45

Chicago Manual of Style (16th Edition):

Rothstein, Patrick E.. “Nucleophilic Palladium Carbenes Utilizing Metal-Ligand Cooperativity Towards Small Molecule Activations</h1>.” 2017. Doctoral Dissertation, University of Notre Dame. Accessed February 28, 2020. https://curate.nd.edu/show/vx021c21m45.

MLA Handbook (7th Edition):

Rothstein, Patrick E.. “Nucleophilic Palladium Carbenes Utilizing Metal-Ligand Cooperativity Towards Small Molecule Activations</h1>.” 2017. Web. 28 Feb 2020.

Vancouver:

Rothstein PE. Nucleophilic Palladium Carbenes Utilizing Metal-Ligand Cooperativity Towards Small Molecule Activations</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2017. [cited 2020 Feb 28]. Available from: https://curate.nd.edu/show/vx021c21m45.

Council of Science Editors:

Rothstein PE. Nucleophilic Palladium Carbenes Utilizing Metal-Ligand Cooperativity Towards Small Molecule Activations</h1>. [Doctoral Dissertation]. University of Notre Dame; 2017. Available from: https://curate.nd.edu/show/vx021c21m45


Georgia Tech

26. Schwimmer, Lauren J. Engineering ligand-receptor pairs for small molecule control of transcription.

Degree: PhD, Chemistry and Biochemistry, 2005, Georgia Tech

 Creating receptors for control of transcription with arbitrary small molecules has widespread applications including gene therapy, biosensors, and enzyme engineering. Using the combination of high… (more)

Subjects/Keywords: Chemical complementation; Ligand-receptor pair; Protein engineering; Retinoid X receptor; Nuclear receptor; Codon randomized libraries; Transcription factors; Protein engineering; Nuclear receptors (Biochemistry); Genetic engineering

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APA (6th Edition):

Schwimmer, L. J. (2005). Engineering ligand-receptor pairs for small molecule control of transcription. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/11651

Chicago Manual of Style (16th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Doctoral Dissertation, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/11651.

MLA Handbook (7th Edition):

Schwimmer, Lauren J. “Engineering ligand-receptor pairs for small molecule control of transcription.” 2005. Web. 28 Feb 2020.

Vancouver:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/11651.

Council of Science Editors:

Schwimmer LJ. Engineering ligand-receptor pairs for small molecule control of transcription. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/11651


University of South Carolina

27. Oberbeck-Oxsher, Fiona Senta. Ligand-Induced Magnetic Changes In Metal Thin Films.

Degree: PhD, Chemistry and Biochemistry, 2016, University of South Carolina

  The investigation of magnetic properties of thin films whose surfaces were modified by organic molecules shows that the addition of any functional group to… (more)

Subjects/Keywords: Chemistry; Ligand; Magnetic; Metal Thin Films

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APA (6th Edition):

Oberbeck-Oxsher, F. S. (2016). Ligand-Induced Magnetic Changes In Metal Thin Films. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/3383

Chicago Manual of Style (16th Edition):

Oberbeck-Oxsher, Fiona Senta. “Ligand-Induced Magnetic Changes In Metal Thin Films.” 2016. Doctoral Dissertation, University of South Carolina. Accessed February 28, 2020. https://scholarcommons.sc.edu/etd/3383.

MLA Handbook (7th Edition):

Oberbeck-Oxsher, Fiona Senta. “Ligand-Induced Magnetic Changes In Metal Thin Films.” 2016. Web. 28 Feb 2020.

Vancouver:

Oberbeck-Oxsher FS. Ligand-Induced Magnetic Changes In Metal Thin Films. [Internet] [Doctoral dissertation]. University of South Carolina; 2016. [cited 2020 Feb 28]. Available from: https://scholarcommons.sc.edu/etd/3383.

Council of Science Editors:

Oberbeck-Oxsher FS. Ligand-Induced Magnetic Changes In Metal Thin Films. [Doctoral Dissertation]. University of South Carolina; 2016. Available from: https://scholarcommons.sc.edu/etd/3383


University of Notre Dame

28. Apryle Marie O'Farrell. Design, Synthesis, and Evaluation of Small Molecules as Potential Inhibitors of Bacterial Cell Wall Biosynthesis</h1>.

Degree: MS, Chemistry and Biochemistry, 2011, University of Notre Dame

  Since the use of penicillin during World War II, the cell wall biosynthesis pathway has been a target for antibiotic treatment. Although hundreds of… (more)

Subjects/Keywords: peptidoglycan; penicillin binding proteins; PBPs

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APA (6th Edition):

O'Farrell, A. M. (2011). Design, Synthesis, and Evaluation of Small Molecules as Potential Inhibitors of Bacterial Cell Wall Biosynthesis</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/wp988g8754c

Chicago Manual of Style (16th Edition):

O'Farrell, Apryle Marie. “Design, Synthesis, and Evaluation of Small Molecules as Potential Inhibitors of Bacterial Cell Wall Biosynthesis</h1>.” 2011. Masters Thesis, University of Notre Dame. Accessed February 28, 2020. https://curate.nd.edu/show/wp988g8754c.

MLA Handbook (7th Edition):

O'Farrell, Apryle Marie. “Design, Synthesis, and Evaluation of Small Molecules as Potential Inhibitors of Bacterial Cell Wall Biosynthesis</h1>.” 2011. Web. 28 Feb 2020.

Vancouver:

O'Farrell AM. Design, Synthesis, and Evaluation of Small Molecules as Potential Inhibitors of Bacterial Cell Wall Biosynthesis</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2011. [cited 2020 Feb 28]. Available from: https://curate.nd.edu/show/wp988g8754c.

Council of Science Editors:

O'Farrell AM. Design, Synthesis, and Evaluation of Small Molecules as Potential Inhibitors of Bacterial Cell Wall Biosynthesis</h1>. [Masters Thesis]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/wp988g8754c


University of Notre Dame

29. Katherine E. Ward. Cytosolic Phospholipase A2: A Mechanistic Study of Lipid Binding and Its Effects on Membrane Morphology</h1>.

Degree: PhD, Chemistry and Biochemistry, 2014, University of Notre Dame

  Lipids participate in cellular homeostasis through selective interactions with proteins, by functioning as second messengers in signaling processes and through the generation of cellular… (more)

Subjects/Keywords: Lipid Binding; cPLA2; Membrane Bending

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APA (6th Edition):

Ward, K. E. (2014). Cytosolic Phospholipase A2: A Mechanistic Study of Lipid Binding and Its Effects on Membrane Morphology</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/6395w665357

Chicago Manual of Style (16th Edition):

Ward, Katherine E.. “Cytosolic Phospholipase A2: A Mechanistic Study of Lipid Binding and Its Effects on Membrane Morphology</h1>.” 2014. Doctoral Dissertation, University of Notre Dame. Accessed February 28, 2020. https://curate.nd.edu/show/6395w665357.

MLA Handbook (7th Edition):

Ward, Katherine E.. “Cytosolic Phospholipase A2: A Mechanistic Study of Lipid Binding and Its Effects on Membrane Morphology</h1>.” 2014. Web. 28 Feb 2020.

Vancouver:

Ward KE. Cytosolic Phospholipase A2: A Mechanistic Study of Lipid Binding and Its Effects on Membrane Morphology</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2014. [cited 2020 Feb 28]. Available from: https://curate.nd.edu/show/6395w665357.

Council of Science Editors:

Ward KE. Cytosolic Phospholipase A2: A Mechanistic Study of Lipid Binding and Its Effects on Membrane Morphology</h1>. [Doctoral Dissertation]. University of Notre Dame; 2014. Available from: https://curate.nd.edu/show/6395w665357

30. Morgan, M. Thomas. Molecular tools for elucidating copper biochemistry: Water-soluble fluorescent probes and robust affinity standards.

Degree: PhD, Chemistry and Biochemistry, 2013, Georgia Tech

 Copper is an essential trace element for living organisms and has both known and additional suspected roles in human health and disease. The current understanding… (more)

Subjects/Keywords: CTAP-2; Sulfonyl fluoride; Sulfonate; Neopentyl; Triarylpyrazoline; Copper(I); Photoinduced electron transfer; Fluorophore; ESPT; Ligand; Aqueous; Copper in the body; Biochemistry; Fluorescent probes

ligand competition experiments to determine the Cu(I)-binding affinities of certain… …aqueous Cu(I) probes by optimizing both the ligand and fluorophore designs 146 5.1… …x28;I)-ligand design 157 5.3.1. Probe design 157 5.3.2. Synthesis 158 5.3.3… …Narylmethanesulfonamide reference fluorophore 175 5.6.4. Combining the best of the ligand and fluorophore… …Ligand design 215 6.2.2. Synthesis and properties of the ligands and their Cu(I)… 

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APA (6th Edition):

Morgan, M. T. (2013). Molecular tools for elucidating copper biochemistry: Water-soluble fluorescent probes and robust affinity standards. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51937

Chicago Manual of Style (16th Edition):

Morgan, M Thomas. “Molecular tools for elucidating copper biochemistry: Water-soluble fluorescent probes and robust affinity standards.” 2013. Doctoral Dissertation, Georgia Tech. Accessed February 28, 2020. http://hdl.handle.net/1853/51937.

MLA Handbook (7th Edition):

Morgan, M Thomas. “Molecular tools for elucidating copper biochemistry: Water-soluble fluorescent probes and robust affinity standards.” 2013. Web. 28 Feb 2020.

Vancouver:

Morgan MT. Molecular tools for elucidating copper biochemistry: Water-soluble fluorescent probes and robust affinity standards. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2020 Feb 28]. Available from: http://hdl.handle.net/1853/51937.

Council of Science Editors:

Morgan MT. Molecular tools for elucidating copper biochemistry: Water-soluble fluorescent probes and robust affinity standards. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/51937

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