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You searched for subject:(Structure activity relationships). Showing records 1 – 30 of 166 total matches.

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Oregon State University

1. Morgan, Jessica L. Characterization of the Structure and Dynamics of the Intrinsically Disordered Dynein Intermediate Chain and its Interactions with Regulatory Binding Partners.

Degree: PhD, Biochemistry & Biophysics, 2015, Oregon State University

 Cells represent microcosms of spatial and temporal structural organization, with the achievement of internal spatial organization relying upon a collection of macromolecular motor complexes to… (more)

Subjects/Keywords: Dynein; Dynein  – Structure-activity relationships

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APA (6th Edition):

Morgan, J. L. (2015). Characterization of the Structure and Dynamics of the Intrinsically Disordered Dynein Intermediate Chain and its Interactions with Regulatory Binding Partners. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/56258

Chicago Manual of Style (16th Edition):

Morgan, Jessica L. “Characterization of the Structure and Dynamics of the Intrinsically Disordered Dynein Intermediate Chain and its Interactions with Regulatory Binding Partners.” 2015. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/56258.

MLA Handbook (7th Edition):

Morgan, Jessica L. “Characterization of the Structure and Dynamics of the Intrinsically Disordered Dynein Intermediate Chain and its Interactions with Regulatory Binding Partners.” 2015. Web. 19 Oct 2020.

Vancouver:

Morgan JL. Characterization of the Structure and Dynamics of the Intrinsically Disordered Dynein Intermediate Chain and its Interactions with Regulatory Binding Partners. [Internet] [Doctoral dissertation]. Oregon State University; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/56258.

Council of Science Editors:

Morgan JL. Characterization of the Structure and Dynamics of the Intrinsically Disordered Dynein Intermediate Chain and its Interactions with Regulatory Binding Partners. [Doctoral Dissertation]. Oregon State University; 2015. Available from: http://hdl.handle.net/1957/56258


Oregon State University

2. Muir, Sean W. Structure-property relationships of layered oxypnictides.

Degree: PhD, Chemistry, 2012, Oregon State University

 Investigating the structure-property relationships of solid state materials can help improve many of the materials we use each day in life. It can also lead… (more)

Subjects/Keywords: Superconductors; Superconductors  – Structure-activity relationships

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APA (6th Edition):

Muir, S. W. (2012). Structure-property relationships of layered oxypnictides. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/29073

Chicago Manual of Style (16th Edition):

Muir, Sean W. “Structure-property relationships of layered oxypnictides.” 2012. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/29073.

MLA Handbook (7th Edition):

Muir, Sean W. “Structure-property relationships of layered oxypnictides.” 2012. Web. 19 Oct 2020.

Vancouver:

Muir SW. Structure-property relationships of layered oxypnictides. [Internet] [Doctoral dissertation]. Oregon State University; 2012. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/29073.

Council of Science Editors:

Muir SW. Structure-property relationships of layered oxypnictides. [Doctoral Dissertation]. Oregon State University; 2012. Available from: http://hdl.handle.net/1957/29073


Oregon State University

3. Hall, Andrea Renee. Biophysical analyses of peroxiredoxins and a partner reductase.

Degree: PhD, Biochemistry and Biophysics, 2010, Oregon State University

 Peroxiredoxins (Prxs) are dominant peroxide-reducing enzymes with two important roles: they protect all organisms from oxidative damage induced by peroxides, and in eukaryotes, they participate… (more)

Subjects/Keywords: peroxiredoxin; Peroxidase  – Structure-activity relationships

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APA (6th Edition):

Hall, A. R. (2010). Biophysical analyses of peroxiredoxins and a partner reductase. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/16146

Chicago Manual of Style (16th Edition):

Hall, Andrea Renee. “Biophysical analyses of peroxiredoxins and a partner reductase.” 2010. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/16146.

MLA Handbook (7th Edition):

Hall, Andrea Renee. “Biophysical analyses of peroxiredoxins and a partner reductase.” 2010. Web. 19 Oct 2020.

Vancouver:

Hall AR. Biophysical analyses of peroxiredoxins and a partner reductase. [Internet] [Doctoral dissertation]. Oregon State University; 2010. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/16146.

Council of Science Editors:

Hall AR. Biophysical analyses of peroxiredoxins and a partner reductase. [Doctoral Dissertation]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/16146


Ryerson University

4. Buenbrazo, Nakita. The development of a molecular toolbox to examine the role of protein O-mannosylation in actinobacteria.

Degree: 2016, Ryerson University

 Protein glycosylation is the most abundant and diverse protein modification that occurs in all domains of life. It is defined as the covalent attachment of… (more)

Subjects/Keywords: Glycoproteins  – Structure-activity relationships.; Glycosylation.; Glycoproteins  – Analysis.

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APA (6th Edition):

Buenbrazo, N. (2016). The development of a molecular toolbox to examine the role of protein O-mannosylation in actinobacteria. (Thesis). Ryerson University. Retrieved from https://digital.library.ryerson.ca/islandora/object/RULA%3A4887

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):

Buenbrazo, Nakita. “The development of a molecular toolbox to examine the role of protein O-mannosylation in actinobacteria.” 2016. Thesis, Ryerson University. Accessed October 19, 2020. https://digital.library.ryerson.ca/islandora/object/RULA%3A4887.

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

MLA Handbook (7th Edition):

Buenbrazo, Nakita. “The development of a molecular toolbox to examine the role of protein O-mannosylation in actinobacteria.” 2016. Web. 19 Oct 2020.

Vancouver:

Buenbrazo N. The development of a molecular toolbox to examine the role of protein O-mannosylation in actinobacteria. [Internet] [Thesis]. Ryerson University; 2016. [cited 2020 Oct 19]. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A4887.

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

Council of Science Editors:

Buenbrazo N. The development of a molecular toolbox to examine the role of protein O-mannosylation in actinobacteria. [Thesis]. Ryerson University; 2016. Available from: https://digital.library.ryerson.ca/islandora/object/RULA%3A4887

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


Oregon State University

5. Yu, Yupei. A quantitative structure activity relationships study of antiinfectives based on the nalidixic acid structure.

Degree: MS, Pharmacy, 1987, Oregon State University

 Nalidixic acid and its derivatives act through inhibition of bacterial DNA gyrase activity. Recently there have been a series of papers reporting the antibacterial activity(more)

Subjects/Keywords: Structure-activity relationships

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APA (6th Edition):

Yu, Y. (1987). A quantitative structure activity relationships study of antiinfectives based on the nalidixic acid structure. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/41091

Chicago Manual of Style (16th Edition):

Yu, Yupei. “A quantitative structure activity relationships study of antiinfectives based on the nalidixic acid structure.” 1987. Masters Thesis, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/41091.

MLA Handbook (7th Edition):

Yu, Yupei. “A quantitative structure activity relationships study of antiinfectives based on the nalidixic acid structure.” 1987. Web. 19 Oct 2020.

Vancouver:

Yu Y. A quantitative structure activity relationships study of antiinfectives based on the nalidixic acid structure. [Internet] [Masters thesis]. Oregon State University; 1987. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/41091.

Council of Science Editors:

Yu Y. A quantitative structure activity relationships study of antiinfectives based on the nalidixic acid structure. [Masters Thesis]. Oregon State University; 1987. Available from: http://hdl.handle.net/1957/41091


Oregon State University

6. Golbek, Thaddeus W. Probing the Biophysical interactions of Anti-Microbial Peptide WLBU2 Using Model Membrane Systems.

Degree: MS, Chemical Engineering, 2015, Oregon State University

 WLBU2 is an engineered cationic amphiphilic peptide that targets Gram-positive and Gram-negative bacteria, and envelopes endotoxin while avoiding other cell types. The exact mechanism of… (more)

Subjects/Keywords: WLBU2; Anti-infective agents  – Structure-activity relationships

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APA (6th Edition):

Golbek, T. W. (2015). Probing the Biophysical interactions of Anti-Microbial Peptide WLBU2 Using Model Membrane Systems. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/56197

Chicago Manual of Style (16th Edition):

Golbek, Thaddeus W. “Probing the Biophysical interactions of Anti-Microbial Peptide WLBU2 Using Model Membrane Systems.” 2015. Masters Thesis, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/56197.

MLA Handbook (7th Edition):

Golbek, Thaddeus W. “Probing the Biophysical interactions of Anti-Microbial Peptide WLBU2 Using Model Membrane Systems.” 2015. Web. 19 Oct 2020.

Vancouver:

Golbek TW. Probing the Biophysical interactions of Anti-Microbial Peptide WLBU2 Using Model Membrane Systems. [Internet] [Masters thesis]. Oregon State University; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/56197.

Council of Science Editors:

Golbek TW. Probing the Biophysical interactions of Anti-Microbial Peptide WLBU2 Using Model Membrane Systems. [Masters Thesis]. Oregon State University; 2015. Available from: http://hdl.handle.net/1957/56197


Oregon State University

7. Serrill, Jeffrey D. Characterization of the Mechanistic Basis for the Cytotoxic Activity of Select Macrocyclic Natural Products against Glioblastoma Cells.

Degree: PhD, Pharmacy, 2015, Oregon State University

 Natural products from both terrestrial and marine sources represent a significant source of novel drug leads, and have previously been developed into clinically-approved agents for… (more)

Subjects/Keywords: Coibamide; Macrocyclic compounds  – Structure-activity relationships

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APA (6th Edition):

Serrill, J. D. (2015). Characterization of the Mechanistic Basis for the Cytotoxic Activity of Select Macrocyclic Natural Products against Glioblastoma Cells. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/57918

Chicago Manual of Style (16th Edition):

Serrill, Jeffrey D. “Characterization of the Mechanistic Basis for the Cytotoxic Activity of Select Macrocyclic Natural Products against Glioblastoma Cells.” 2015. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/57918.

MLA Handbook (7th Edition):

Serrill, Jeffrey D. “Characterization of the Mechanistic Basis for the Cytotoxic Activity of Select Macrocyclic Natural Products against Glioblastoma Cells.” 2015. Web. 19 Oct 2020.

Vancouver:

Serrill JD. Characterization of the Mechanistic Basis for the Cytotoxic Activity of Select Macrocyclic Natural Products against Glioblastoma Cells. [Internet] [Doctoral dissertation]. Oregon State University; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/57918.

Council of Science Editors:

Serrill JD. Characterization of the Mechanistic Basis for the Cytotoxic Activity of Select Macrocyclic Natural Products against Glioblastoma Cells. [Doctoral Dissertation]. Oregon State University; 2015. Available from: http://hdl.handle.net/1957/57918


Anna University

8. Senbagamalar J. On topological indices of Molecular graphs;.

Degree: On topological indices of Molecular graphs, 2015, Anna University

The representation of an object giving information only about the newlinenumber of elements composing it and their connectivity is named as newlinetopological representation of an… (more)

Subjects/Keywords: Molecular graph; quantitative structure activity relationships

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APA (6th Edition):

J, S. (2015). On topological indices of Molecular graphs;. (Thesis). Anna University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/33720

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):

J, Senbagamalar. “On topological indices of Molecular graphs;.” 2015. Thesis, Anna University. Accessed October 19, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/33720.

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

MLA Handbook (7th Edition):

J, Senbagamalar. “On topological indices of Molecular graphs;.” 2015. Web. 19 Oct 2020.

Vancouver:

J S. On topological indices of Molecular graphs;. [Internet] [Thesis]. Anna University; 2015. [cited 2020 Oct 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/33720.

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

Council of Science Editors:

J S. On topological indices of Molecular graphs;. [Thesis]. Anna University; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/33720

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


Oregon State University

9. Gatimu, Alvin J. Structure-property relationships in oxides containing select platinum group metals.

Degree: PhD, Chemistry, 2012, Oregon State University

 Oxide materials exhibit a wide variety of structures and properties. In particular, transition metal oxides tend to be highly stable while exhibiting a wide range… (more)

Subjects/Keywords: Oxides; Transition metal oxides  – Structure-activity relationships

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APA (6th Edition):

Gatimu, A. J. (2012). Structure-property relationships in oxides containing select platinum group metals. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/31770

Chicago Manual of Style (16th Edition):

Gatimu, Alvin J. “Structure-property relationships in oxides containing select platinum group metals.” 2012. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/31770.

MLA Handbook (7th Edition):

Gatimu, Alvin J. “Structure-property relationships in oxides containing select platinum group metals.” 2012. Web. 19 Oct 2020.

Vancouver:

Gatimu AJ. Structure-property relationships in oxides containing select platinum group metals. [Internet] [Doctoral dissertation]. Oregon State University; 2012. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/31770.

Council of Science Editors:

Gatimu AJ. Structure-property relationships in oxides containing select platinum group metals. [Doctoral Dissertation]. Oregon State University; 2012. Available from: http://hdl.handle.net/1957/31770


Oregon State University

10. Grajczyk, Rosa. Structure-property relationships of YbFe₂O₄-type layered transition metal oxides.

Degree: PhD, Chemistry, 2014, Oregon State University

 The structure–property relationships of solid solutions within the YbFe₂O₄ family of compounds have been studied in relation to their optical, dielectric and magnetic properties. This… (more)

Subjects/Keywords: Chemistry; Transition metal oxides  – Structure-activity relationships

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APA (6th Edition):

Grajczyk, R. (2014). Structure-property relationships of YbFe₂O₄-type layered transition metal oxides. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/48547

Chicago Manual of Style (16th Edition):

Grajczyk, Rosa. “Structure-property relationships of YbFe₂O₄-type layered transition metal oxides.” 2014. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/48547.

MLA Handbook (7th Edition):

Grajczyk, Rosa. “Structure-property relationships of YbFe₂O₄-type layered transition metal oxides.” 2014. Web. 19 Oct 2020.

Vancouver:

Grajczyk R. Structure-property relationships of YbFe₂O₄-type layered transition metal oxides. [Internet] [Doctoral dissertation]. Oregon State University; 2014. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/48547.

Council of Science Editors:

Grajczyk R. Structure-property relationships of YbFe₂O₄-type layered transition metal oxides. [Doctoral Dissertation]. Oregon State University; 2014. Available from: http://hdl.handle.net/1957/48547


Oregon State University

11. Smith, Andrew E. (Andrew Earnest). Functional transition metal oxides : structure-property relationships.

Degree: PhD, Chemistry, 2010, Oregon State University

 Transition metal oxides are an important class of materials for the wide variety optical, electrical, dielectric, magnetic, and thermal properties observed. Their unique structure-property relationships(more)

Subjects/Keywords: Oxides; Transition metal oxides  – Structure-activity relationships

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APA (6th Edition):

Smith, A. E. (. E. (2010). Functional transition metal oxides : structure-property relationships. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/16293

Chicago Manual of Style (16th Edition):

Smith, Andrew E (Andrew Earnest). “Functional transition metal oxides : structure-property relationships.” 2010. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/16293.

MLA Handbook (7th Edition):

Smith, Andrew E (Andrew Earnest). “Functional transition metal oxides : structure-property relationships.” 2010. Web. 19 Oct 2020.

Vancouver:

Smith AE(E. Functional transition metal oxides : structure-property relationships. [Internet] [Doctoral dissertation]. Oregon State University; 2010. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/16293.

Council of Science Editors:

Smith AE(E. Functional transition metal oxides : structure-property relationships. [Doctoral Dissertation]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/16293


University of Missouri – Columbia

12. Cao, Renzhi. Genome data analysis, protein function and structure prediction by machine learning techniques.

Degree: 2016, University of Missouri – Columbia

 The raw information of a typical human genome has been generated at 2001 by Human Genome Project. However, since there are a huge amount of… (more)

Subjects/Keywords: Genomes  – Data processing; Proteins  – Structure-activity relationships

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APA (6th Edition):

Cao, R. (2016). Genome data analysis, protein function and structure prediction by machine learning techniques. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/57021

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):

Cao, Renzhi. “Genome data analysis, protein function and structure prediction by machine learning techniques.” 2016. Thesis, University of Missouri – Columbia. Accessed October 19, 2020. https://doi.org/10.32469/10355/57021.

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

MLA Handbook (7th Edition):

Cao, Renzhi. “Genome data analysis, protein function and structure prediction by machine learning techniques.” 2016. Web. 19 Oct 2020.

Vancouver:

Cao R. Genome data analysis, protein function and structure prediction by machine learning techniques. [Internet] [Thesis]. University of Missouri – Columbia; 2016. [cited 2020 Oct 19]. Available from: https://doi.org/10.32469/10355/57021.

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

Council of Science Editors:

Cao R. Genome data analysis, protein function and structure prediction by machine learning techniques. [Thesis]. University of Missouri – Columbia; 2016. Available from: https://doi.org/10.32469/10355/57021

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


University of Minnesota

13. Zhu, Qianhong. QSAR for anticancer activity by using mathematical descriptors.

Degree: MS, Chemistry, 2010, University of Minnesota

University of Minnesota M.S. thesis. July 2010. Major: Chemistry. Advisor: Subhash C Basak. 1 computer file (PDF); v, 94 pages, appendices I-II. Ill. (some col.)… (more)

Subjects/Keywords: Quantitative structure-activity relationships (QSARs); Physicochemical properties; Molecules; Biological activity; Chemistry

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APA (6th Edition):

Zhu, Q. (2010). QSAR for anticancer activity by using mathematical descriptors. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/93639

Chicago Manual of Style (16th Edition):

Zhu, Qianhong. “QSAR for anticancer activity by using mathematical descriptors.” 2010. Masters Thesis, University of Minnesota. Accessed October 19, 2020. http://purl.umn.edu/93639.

MLA Handbook (7th Edition):

Zhu, Qianhong. “QSAR for anticancer activity by using mathematical descriptors.” 2010. Web. 19 Oct 2020.

Vancouver:

Zhu Q. QSAR for anticancer activity by using mathematical descriptors. [Internet] [Masters thesis]. University of Minnesota; 2010. [cited 2020 Oct 19]. Available from: http://purl.umn.edu/93639.

Council of Science Editors:

Zhu Q. QSAR for anticancer activity by using mathematical descriptors. [Masters Thesis]. University of Minnesota; 2010. Available from: http://purl.umn.edu/93639


North Carolina State University

14. Richards, Justin James. Design, Synthesis, and Biological Evaluation of Novel Anti-Biofilm Molecules Derived from the Oroidin Alkaloids.

Degree: PhD, Chemistry, 2009, North Carolina State University

 Bacterial biofilms are a surface attached community of microorganisms that are protected by an extracellular matrix of biomolecules. Within a biofilm state, bacteria are more… (more)

Subjects/Keywords: biological activity; biofilms; bacteria; structure activity-relationships; natural products

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APA (6th Edition):

Richards, J. J. (2009). Design, Synthesis, and Biological Evaluation of Novel Anti-Biofilm Molecules Derived from the Oroidin Alkaloids. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5829

Chicago Manual of Style (16th Edition):

Richards, Justin James. “Design, Synthesis, and Biological Evaluation of Novel Anti-Biofilm Molecules Derived from the Oroidin Alkaloids.” 2009. Doctoral Dissertation, North Carolina State University. Accessed October 19, 2020. http://www.lib.ncsu.edu/resolver/1840.16/5829.

MLA Handbook (7th Edition):

Richards, Justin James. “Design, Synthesis, and Biological Evaluation of Novel Anti-Biofilm Molecules Derived from the Oroidin Alkaloids.” 2009. Web. 19 Oct 2020.

Vancouver:

Richards JJ. Design, Synthesis, and Biological Evaluation of Novel Anti-Biofilm Molecules Derived from the Oroidin Alkaloids. [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2020 Oct 19]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5829.

Council of Science Editors:

Richards JJ. Design, Synthesis, and Biological Evaluation of Novel Anti-Biofilm Molecules Derived from the Oroidin Alkaloids. [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5829


University of Victoria

15. Faris, Jonathan Scott. Characterization of the DNA binding properties of the thyroid hormone receptor.

Degree: Department of Biochemistry and Microbiology, 2018, University of Victoria

 This thesis describes work done with the thyroid hormone receptor (TR), a nuclear protein which binds to specific DNA sequences and regulates transcription in response… (more)

Subjects/Keywords: DNA; Structure; Nucleoproteins; Structure-activity relationships; DNA-protein interactions; Thyroid hormones

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APA (6th Edition):

Faris, J. S. (2018). Characterization of the DNA binding properties of the thyroid hormone receptor. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/9701

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):

Faris, Jonathan Scott. “Characterization of the DNA binding properties of the thyroid hormone receptor.” 2018. Thesis, University of Victoria. Accessed October 19, 2020. https://dspace.library.uvic.ca//handle/1828/9701.

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

MLA Handbook (7th Edition):

Faris, Jonathan Scott. “Characterization of the DNA binding properties of the thyroid hormone receptor.” 2018. Web. 19 Oct 2020.

Vancouver:

Faris JS. Characterization of the DNA binding properties of the thyroid hormone receptor. [Internet] [Thesis]. University of Victoria; 2018. [cited 2020 Oct 19]. Available from: https://dspace.library.uvic.ca//handle/1828/9701.

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

Council of Science Editors:

Faris JS. Characterization of the DNA binding properties of the thyroid hormone receptor. [Thesis]. University of Victoria; 2018. Available from: https://dspace.library.uvic.ca//handle/1828/9701

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

16. A. Dhavan. SYNTHETIC STUDIES TOWARDS THE NATURAL PRODUCT LEOPOLIC ACID A.

Degree: 2015, Università degli Studi di Milano

 The need to develop new fungicides remains a major driving force as fungal plant pathogens continue to develop resistance against existing fungicides at great speed,… (more)

Subjects/Keywords: total synthesis; antifungal activity; antimicrobial activity; structure-activity relationships; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Dhavan, A. (2015). SYNTHETIC STUDIES TOWARDS THE NATURAL PRODUCT LEOPOLIC ACID A. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/345442

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):

Dhavan, A.. “SYNTHETIC STUDIES TOWARDS THE NATURAL PRODUCT LEOPOLIC ACID A.” 2015. Thesis, Università degli Studi di Milano. Accessed October 19, 2020. http://hdl.handle.net/2434/345442.

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

MLA Handbook (7th Edition):

Dhavan, A.. “SYNTHETIC STUDIES TOWARDS THE NATURAL PRODUCT LEOPOLIC ACID A.” 2015. Web. 19 Oct 2020.

Vancouver:

Dhavan A. SYNTHETIC STUDIES TOWARDS THE NATURAL PRODUCT LEOPOLIC ACID A. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/2434/345442.

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

Council of Science Editors:

Dhavan A. SYNTHETIC STUDIES TOWARDS THE NATURAL PRODUCT LEOPOLIC ACID A. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/345442

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


Penn State University

17. Bennett, Samantha Michelle. Chemesthesis and bitterness of natural and synthetic anti-inflammatory stimuli.

Degree: 2012, Penn State University

 Recently, Gibson’s ecological approach to classifying chemosensation has regained popularity. In his model, sensations are not classified on the basis of anatomy, but rather by… (more)

Subjects/Keywords: Chemesthesis; Bitterness; Ibuprofen; Olive Oil; Sensory Evaluation; Oleocanthal; Structure Activity Relationships

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APA (6th Edition):

Bennett, S. M. (2012). Chemesthesis and bitterness of natural and synthetic anti-inflammatory stimuli. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13754

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):

Bennett, Samantha Michelle. “Chemesthesis and bitterness of natural and synthetic anti-inflammatory stimuli.” 2012. Thesis, Penn State University. Accessed October 19, 2020. https://submit-etda.libraries.psu.edu/catalog/13754.

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

MLA Handbook (7th Edition):

Bennett, Samantha Michelle. “Chemesthesis and bitterness of natural and synthetic anti-inflammatory stimuli.” 2012. Web. 19 Oct 2020.

Vancouver:

Bennett SM. Chemesthesis and bitterness of natural and synthetic anti-inflammatory stimuli. [Internet] [Thesis]. Penn State University; 2012. [cited 2020 Oct 19]. Available from: https://submit-etda.libraries.psu.edu/catalog/13754.

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

Council of Science Editors:

Bennett SM. Chemesthesis and bitterness of natural and synthetic anti-inflammatory stimuli. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/13754

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


Oregon State University

18. Geierstanger, Bernhard H. Base specific binding of copper (II) to Z-DNA : 1.3 A single crystal structure of d(m⁵CGUAm⁵CG) soaked with CuCl₂.

Degree: MS, Biochemistry and Biophysics, 1990, Oregon State University

Subjects/Keywords: Copper  – Structure-activity relationships

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APA (6th Edition):

Geierstanger, B. H. (1990). Base specific binding of copper (II) to Z-DNA : 1.3 A single crystal structure of d(m⁵CGUAm⁵CG) soaked with CuCl₂. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/38128

Chicago Manual of Style (16th Edition):

Geierstanger, Bernhard H. “Base specific binding of copper (II) to Z-DNA : 1.3 A single crystal structure of d(m⁵CGUAm⁵CG) soaked with CuCl₂.” 1990. Masters Thesis, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/38128.

MLA Handbook (7th Edition):

Geierstanger, Bernhard H. “Base specific binding of copper (II) to Z-DNA : 1.3 A single crystal structure of d(m⁵CGUAm⁵CG) soaked with CuCl₂.” 1990. Web. 19 Oct 2020.

Vancouver:

Geierstanger BH. Base specific binding of copper (II) to Z-DNA : 1.3 A single crystal structure of d(m⁵CGUAm⁵CG) soaked with CuCl₂. [Internet] [Masters thesis]. Oregon State University; 1990. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/38128.

Council of Science Editors:

Geierstanger BH. Base specific binding of copper (II) to Z-DNA : 1.3 A single crystal structure of d(m⁵CGUAm⁵CG) soaked with CuCl₂. [Masters Thesis]. Oregon State University; 1990. Available from: http://hdl.handle.net/1957/38128


University of Delaware

19. Naranjo, Andrea N. Stability and activity of a GPCR in vivo and in membrane mimetic environments.

Degree: PhD, University of Delaware, Department of Chemical and Biomolecular Engineering, 2014, University of Delaware

 G protein-coupled receptors (GPCRs) are integral membrane proteins involved in cellular signaling and constitute major drug targets. Despite their importance, the relationship between structure and… (more)

Subjects/Keywords: Cell receptors  – Structure-activity relationships.; Ligand binding (Biochemistry); Adenosine.; Lipids.

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APA (6th Edition):

Naranjo, A. N. (2014). Stability and activity of a GPCR in vivo and in membrane mimetic environments. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/16816

Chicago Manual of Style (16th Edition):

Naranjo, Andrea N. “Stability and activity of a GPCR in vivo and in membrane mimetic environments.” 2014. Doctoral Dissertation, University of Delaware. Accessed October 19, 2020. http://udspace.udel.edu/handle/19716/16816.

MLA Handbook (7th Edition):

Naranjo, Andrea N. “Stability and activity of a GPCR in vivo and in membrane mimetic environments.” 2014. Web. 19 Oct 2020.

Vancouver:

Naranjo AN. Stability and activity of a GPCR in vivo and in membrane mimetic environments. [Internet] [Doctoral dissertation]. University of Delaware; 2014. [cited 2020 Oct 19]. Available from: http://udspace.udel.edu/handle/19716/16816.

Council of Science Editors:

Naranjo AN. Stability and activity of a GPCR in vivo and in membrane mimetic environments. [Doctoral Dissertation]. University of Delaware; 2014. Available from: http://udspace.udel.edu/handle/19716/16816


Columbia University

20. McGoldrick, Luke Lawrence Reedy. Structural Analyses of the Transient Receptor Potential Channels TRPV3 and TRPV6.

Degree: 2019, Columbia University

 Transient receptor potential (TRP) channels comprise a superfamily of cation-selective ion channels that are largely calcium (Ca2+) permeable and that play diverse physiological roles ranging… (more)

Subjects/Keywords: Biochemistry; Molecular biology; TRP channels; Structure-activity relationships (Biochemistry); Ion channels

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APA (6th Edition):

McGoldrick, L. L. R. (2019). Structural Analyses of the Transient Receptor Potential Channels TRPV3 and TRPV6. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-d1x5-rw78

Chicago Manual of Style (16th Edition):

McGoldrick, Luke Lawrence Reedy. “Structural Analyses of the Transient Receptor Potential Channels TRPV3 and TRPV6.” 2019. Doctoral Dissertation, Columbia University. Accessed October 19, 2020. https://doi.org/10.7916/d8-d1x5-rw78.

MLA Handbook (7th Edition):

McGoldrick, Luke Lawrence Reedy. “Structural Analyses of the Transient Receptor Potential Channels TRPV3 and TRPV6.” 2019. Web. 19 Oct 2020.

Vancouver:

McGoldrick LLR. Structural Analyses of the Transient Receptor Potential Channels TRPV3 and TRPV6. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2020 Oct 19]. Available from: https://doi.org/10.7916/d8-d1x5-rw78.

Council of Science Editors:

McGoldrick LLR. Structural Analyses of the Transient Receptor Potential Channels TRPV3 and TRPV6. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-d1x5-rw78


Virginia Tech

21. Morris, Emily A. Structure-activity relationship studies and biological evaluation of selective sphingosine kinase inhibitors.

Degree: MS, Chemistry, 2015, Virginia Tech

 Sphingosine 1-phosphate (S1P) has become a prevalent drug discovery target due to studies implicating it to several disease pathologies such as fibrosis, sickle cell disease,… (more)

Subjects/Keywords: sphingosine 1-phosphate; sphingosine kinase inhibitors; structure-activity relationships; guanidine inhibitors

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APA (6th Edition):

Morris, E. A. (2015). Structure-activity relationship studies and biological evaluation of selective sphingosine kinase inhibitors. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/73491

Chicago Manual of Style (16th Edition):

Morris, Emily A. “Structure-activity relationship studies and biological evaluation of selective sphingosine kinase inhibitors.” 2015. Masters Thesis, Virginia Tech. Accessed October 19, 2020. http://hdl.handle.net/10919/73491.

MLA Handbook (7th Edition):

Morris, Emily A. “Structure-activity relationship studies and biological evaluation of selective sphingosine kinase inhibitors.” 2015. Web. 19 Oct 2020.

Vancouver:

Morris EA. Structure-activity relationship studies and biological evaluation of selective sphingosine kinase inhibitors. [Internet] [Masters thesis]. Virginia Tech; 2015. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10919/73491.

Council of Science Editors:

Morris EA. Structure-activity relationship studies and biological evaluation of selective sphingosine kinase inhibitors. [Masters Thesis]. Virginia Tech; 2015. Available from: http://hdl.handle.net/10919/73491


University of Sydney

22. Tran, Anh. Development of new drug leads for tuberculosis .

Degree: 2014, University of Sydney

 Tuberculosis (TB), caused by infection with the bacterium Mycobacterium tuberculosis, has re-emerged as a global health risk with a significant proportion of new TB cases… (more)

Subjects/Keywords: Tuberculosis; Drug discovery; Structure-activity relationships; Enzyme inhibitors

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APA (6th Edition):

Tran, A. (2014). Development of new drug leads for tuberculosis . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/11637

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):

Tran, Anh. “Development of new drug leads for tuberculosis .” 2014. Thesis, University of Sydney. Accessed October 19, 2020. http://hdl.handle.net/2123/11637.

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

MLA Handbook (7th Edition):

Tran, Anh. “Development of new drug leads for tuberculosis .” 2014. Web. 19 Oct 2020.

Vancouver:

Tran A. Development of new drug leads for tuberculosis . [Internet] [Thesis]. University of Sydney; 2014. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/2123/11637.

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

Council of Science Editors:

Tran A. Development of new drug leads for tuberculosis . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/11637

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


Univerzitet u Beogradu

23. Vitorović-Todorović, Maja, 1977-. Racionalni dizajn i sinteza jedinjenja sa strukturnim skeletom amida aroilakrilnih kiselina koja ispoljavaju antiholinesteraznu, antitubulinsku i antiproliferativnu aktivnost.

Degree: Hemijski fakultet, 2016, Univerzitet u Beogradu

Organska hemija - Medicinska hemija / Organic chemistry - Medicinal chemistry

U ovoj tezi su opisane različite strukturne modifikacije aroilakrilnih kiselina, zasnovane na relativno jednostavnim… (more)

Subjects/Keywords: aroylacrylic acid amides; Michaels addition; anticholinesterase; antitubuline and antiproliferative activity; 3D structure – activity relationships; docking

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APA (6th Edition):

Vitorović-Todorović, Maja, 1. (2016). Racionalni dizajn i sinteza jedinjenja sa strukturnim skeletom amida aroilakrilnih kiselina koja ispoljavaju antiholinesteraznu, antitubulinsku i antiproliferativnu aktivnost. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:11564/bdef:Content/get

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):

Vitorović-Todorović, Maja, 1977-. “Racionalni dizajn i sinteza jedinjenja sa strukturnim skeletom amida aroilakrilnih kiselina koja ispoljavaju antiholinesteraznu, antitubulinsku i antiproliferativnu aktivnost.” 2016. Thesis, Univerzitet u Beogradu. Accessed October 19, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:11564/bdef:Content/get.

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

MLA Handbook (7th Edition):

Vitorović-Todorović, Maja, 1977-. “Racionalni dizajn i sinteza jedinjenja sa strukturnim skeletom amida aroilakrilnih kiselina koja ispoljavaju antiholinesteraznu, antitubulinsku i antiproliferativnu aktivnost.” 2016. Web. 19 Oct 2020.

Vancouver:

Vitorović-Todorović, Maja 1. Racionalni dizajn i sinteza jedinjenja sa strukturnim skeletom amida aroilakrilnih kiselina koja ispoljavaju antiholinesteraznu, antitubulinsku i antiproliferativnu aktivnost. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2020 Oct 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11564/bdef:Content/get.

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

Council of Science Editors:

Vitorović-Todorović, Maja 1. Racionalni dizajn i sinteza jedinjenja sa strukturnim skeletom amida aroilakrilnih kiselina koja ispoljavaju antiholinesteraznu, antitubulinsku i antiproliferativnu aktivnost. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11564/bdef:Content/get

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


Michigan State University

24. Opron, Kristopher. The flexibility-rigidity index (FRI : theory and applications.

Degree: 2016, Michigan State University

Thesis Ph. D. Michigan State University. Biochemistry and Molecular Biology 2016

Since the first protein structures were solved in the 1950s, the protein data bank… (more)

Subjects/Keywords: Proteins – Structure-activity relationships – Research – Methodology; Proteins – Structure; Protein folding; Proteins – Stability; Biophysics; Mathematics; Biochemistry

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APA (6th Edition):

Opron, K. (2016). The flexibility-rigidity index (FRI : theory and applications. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:4005

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):

Opron, Kristopher. “The flexibility-rigidity index (FRI : theory and applications.” 2016. Thesis, Michigan State University. Accessed October 19, 2020. http://etd.lib.msu.edu/islandora/object/etd:4005.

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

MLA Handbook (7th Edition):

Opron, Kristopher. “The flexibility-rigidity index (FRI : theory and applications.” 2016. Web. 19 Oct 2020.

Vancouver:

Opron K. The flexibility-rigidity index (FRI : theory and applications. [Internet] [Thesis]. Michigan State University; 2016. [cited 2020 Oct 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:4005.

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

Council of Science Editors:

Opron K. The flexibility-rigidity index (FRI : theory and applications. [Thesis]. Michigan State University; 2016. Available from: http://etd.lib.msu.edu/islandora/object/etd:4005

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


Northeastern University

25. Huo, Ran. Characterizing the assembly and disruption of protein-nucleic acid complexes using atomic force microscopy in liquid.

Degree: PhD, Department of Physics, 2016, Northeastern University

 Atomic force microscopy (AFM) is a powerful tool for investigating DNA structure and DNA-protein interactions. In this work, we characterize the assembly and disruption of… (more)

Subjects/Keywords: FACT; HMGB; nucleosomes; optical tweezers; DNA-binding proteins; Structure-activity relationships; Protein binding; Atomic force microscopy; Chromatin; Structure-activity relationships; Eukaryotic cells; Nucleic acids

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APA (6th Edition):

Huo, R. (2016). Characterizing the assembly and disruption of protein-nucleic acid complexes using atomic force microscopy in liquid. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20235008

Chicago Manual of Style (16th Edition):

Huo, Ran. “Characterizing the assembly and disruption of protein-nucleic acid complexes using atomic force microscopy in liquid.” 2016. Doctoral Dissertation, Northeastern University. Accessed October 19, 2020. http://hdl.handle.net/2047/D20235008.

MLA Handbook (7th Edition):

Huo, Ran. “Characterizing the assembly and disruption of protein-nucleic acid complexes using atomic force microscopy in liquid.” 2016. Web. 19 Oct 2020.

Vancouver:

Huo R. Characterizing the assembly and disruption of protein-nucleic acid complexes using atomic force microscopy in liquid. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/2047/D20235008.

Council of Science Editors:

Huo R. Characterizing the assembly and disruption of protein-nucleic acid complexes using atomic force microscopy in liquid. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20235008


University of Missouri – Columbia

26. Ndubuka, Kelly. Divalent ion-binding and thermal stability studies on rat [beta]-parvalbumin and the evidence of influential distant amino acid residues affecting CD site ion affinity.

Degree: 2011, University of Missouri – Columbia

 Parvalbumins (PVs) are vertebrate-specific proteins (Mr 12,000), which harbor two EF-hand motifs known as the CD and EF sites. Although the CD and EF sites… (more)

Subjects/Keywords: Albumins  – Structure-activity relationships; Volumetric analysis; Calorimetry; Calmodulin; Structure-activity relationships (Biochemistry); Amino acids  – Effect of heat on; Temperature  – Physiological effect; Rats  – Physiology  – Experiments

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APA (6th Edition):

Ndubuka, K. (2011). Divalent ion-binding and thermal stability studies on rat [beta]-parvalbumin and the evidence of influential distant amino acid residues affecting CD site ion affinity. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/11499

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):

Ndubuka, Kelly. “Divalent ion-binding and thermal stability studies on rat [beta]-parvalbumin and the evidence of influential distant amino acid residues affecting CD site ion affinity.” 2011. Thesis, University of Missouri – Columbia. Accessed October 19, 2020. http://hdl.handle.net/10355/11499.

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

MLA Handbook (7th Edition):

Ndubuka, Kelly. “Divalent ion-binding and thermal stability studies on rat [beta]-parvalbumin and the evidence of influential distant amino acid residues affecting CD site ion affinity.” 2011. Web. 19 Oct 2020.

Vancouver:

Ndubuka K. Divalent ion-binding and thermal stability studies on rat [beta]-parvalbumin and the evidence of influential distant amino acid residues affecting CD site ion affinity. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/10355/11499.

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

Council of Science Editors:

Ndubuka K. Divalent ion-binding and thermal stability studies on rat [beta]-parvalbumin and the evidence of influential distant amino acid residues affecting CD site ion affinity. [Thesis]. University of Missouri – Columbia; 2011. Available from: http://hdl.handle.net/10355/11499

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


Vanderbilt University

27. Dutter, Brendan Frank. Chemical biology of bacterial metal acquisition and homeostasis.

Degree: PhD, Chemical and Physical Biology, 2016, Vanderbilt University

 Metals, such as iron, zinc, and manganese, are required for bacterial function and survival. Bacteria have evolved systems to acquire metals from the environments they… (more)

Subjects/Keywords: siderophore; bacteria; structure-activity relationships; target identification; heme; chemical biology; click chemistry; photoaffinity label

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APA (6th Edition):

Dutter, B. F. (2016). Chemical biology of bacterial metal acquisition and homeostasis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13459

Chicago Manual of Style (16th Edition):

Dutter, Brendan Frank. “Chemical biology of bacterial metal acquisition and homeostasis.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed October 19, 2020. http://hdl.handle.net/1803/13459.

MLA Handbook (7th Edition):

Dutter, Brendan Frank. “Chemical biology of bacterial metal acquisition and homeostasis.” 2016. Web. 19 Oct 2020.

Vancouver:

Dutter BF. Chemical biology of bacterial metal acquisition and homeostasis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1803/13459.

Council of Science Editors:

Dutter BF. Chemical biology of bacterial metal acquisition and homeostasis. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/13459


University of California – Riverside

28. Palchak, Zachary. Advancing Methods to Synthesize Nitrogen-Containing Small Molecules for Catalysis and as Potential Therapeutics.

Degree: Chemistry, 2018, University of California – Riverside

 Analysis of the current top grossing pharmaceuticals finds that a vast number of them contain amines. As a result, the development of methodologies for the… (more)

Subjects/Keywords: Organic chemistry; Catalysis; Nitrogen; Process Chemistry; Small Molecules; Structure Activity Relationships; Therapeutics

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APA (6th Edition):

Palchak, Z. (2018). Advancing Methods to Synthesize Nitrogen-Containing Small Molecules for Catalysis and as Potential Therapeutics. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/3f14t4f6

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):

Palchak, Zachary. “Advancing Methods to Synthesize Nitrogen-Containing Small Molecules for Catalysis and as Potential Therapeutics.” 2018. Thesis, University of California – Riverside. Accessed October 19, 2020. http://www.escholarship.org/uc/item/3f14t4f6.

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

MLA Handbook (7th Edition):

Palchak, Zachary. “Advancing Methods to Synthesize Nitrogen-Containing Small Molecules for Catalysis and as Potential Therapeutics.” 2018. Web. 19 Oct 2020.

Vancouver:

Palchak Z. Advancing Methods to Synthesize Nitrogen-Containing Small Molecules for Catalysis and as Potential Therapeutics. [Internet] [Thesis]. University of California – Riverside; 2018. [cited 2020 Oct 19]. Available from: http://www.escholarship.org/uc/item/3f14t4f6.

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

Council of Science Editors:

Palchak Z. Advancing Methods to Synthesize Nitrogen-Containing Small Molecules for Catalysis and as Potential Therapeutics. [Thesis]. University of California – Riverside; 2018. Available from: http://www.escholarship.org/uc/item/3f14t4f6

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


Oregon State University

29. Jiang, Peng. Structure-property relationships of oxides with hexagonal AMO₃ and brownmillerite related structures.

Degree: PhD, Chemistry, 2012, Oregon State University

 Transition metal oxides exhibit potential in various application fields due to the special d-electrons. Solid state chemistry focuses on discovering the structure-property relationships. The work… (more)

Subjects/Keywords: oxides with hexagonal AMO3 related structures; Transition metal oxides  – Structure-activity relationships

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APA (6th Edition):

Jiang, P. (2012). Structure-property relationships of oxides with hexagonal AMO₃ and brownmillerite related structures. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/33641

Chicago Manual of Style (16th Edition):

Jiang, Peng. “Structure-property relationships of oxides with hexagonal AMO₃ and brownmillerite related structures.” 2012. Doctoral Dissertation, Oregon State University. Accessed October 19, 2020. http://hdl.handle.net/1957/33641.

MLA Handbook (7th Edition):

Jiang, Peng. “Structure-property relationships of oxides with hexagonal AMO₃ and brownmillerite related structures.” 2012. Web. 19 Oct 2020.

Vancouver:

Jiang P. Structure-property relationships of oxides with hexagonal AMO₃ and brownmillerite related structures. [Internet] [Doctoral dissertation]. Oregon State University; 2012. [cited 2020 Oct 19]. Available from: http://hdl.handle.net/1957/33641.

Council of Science Editors:

Jiang P. Structure-property relationships of oxides with hexagonal AMO₃ and brownmillerite related structures. [Doctoral Dissertation]. Oregon State University; 2012. Available from: http://hdl.handle.net/1957/33641


University of Iowa

30. Schwanz, Heidi Ann. Structural features of fluoroquinolone-class antibiotics that affect lethal activities and DNA binding.

Degree: PhD, Pharmacy, 2012, University of Iowa

  Fluoroquinolones, broad-spectrum bactericidal antibiotics, exert their effects by inhibiting type II topoisomerases through the formation of a fluoroquinolone-DNA-topoisomerase ternary complex. Recently, newer, structurally unique… (more)

Subjects/Keywords: antibiotics; fluoroquinolone resistance; fluoroquinolones; quinazoline; structure activity relationships; topoisomerases; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Schwanz, H. A. (2012). Structural features of fluoroquinolone-class antibiotics that affect lethal activities and DNA binding. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1395

Chicago Manual of Style (16th Edition):

Schwanz, Heidi Ann. “Structural features of fluoroquinolone-class antibiotics that affect lethal activities and DNA binding.” 2012. Doctoral Dissertation, University of Iowa. Accessed October 19, 2020. https://ir.uiowa.edu/etd/1395.

MLA Handbook (7th Edition):

Schwanz, Heidi Ann. “Structural features of fluoroquinolone-class antibiotics that affect lethal activities and DNA binding.” 2012. Web. 19 Oct 2020.

Vancouver:

Schwanz HA. Structural features of fluoroquinolone-class antibiotics that affect lethal activities and DNA binding. [Internet] [Doctoral dissertation]. University of Iowa; 2012. [cited 2020 Oct 19]. Available from: https://ir.uiowa.edu/etd/1395.

Council of Science Editors:

Schwanz HA. Structural features of fluoroquinolone-class antibiotics that affect lethal activities and DNA binding. [Doctoral Dissertation]. University of Iowa; 2012. Available from: https://ir.uiowa.edu/etd/1395

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