Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for +publisher:"University of Arizona" +contributor:("Hruby, Victor J."). Showing records 1 – 30 of 75 total matches.

[1] [2] [3]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters


University of Arizona

1. Nyberg, Joel Benjamin. Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides .

Degree: 2013, University of Arizona

 The melanocortin 3 and 4 receptors share 58% overall amino acid identity and 76% similarity. This high level of similarity between the MC3R and the… (more)

Subjects/Keywords: Melancortins; Melanocortin 3; Melanocortin 3 selective ligands; Peptides; Chemistry; C-terminal modification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nyberg, J. B. (2013). Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/283606

Chicago Manual of Style (16th Edition):

Nyberg, Joel Benjamin. “Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides .” 2013. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/283606.

MLA Handbook (7th Edition):

Nyberg, Joel Benjamin. “Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides .” 2013. Web. 28 Nov 2020.

Vancouver:

Nyberg JB. Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/283606.

Council of Science Editors:

Nyberg JB. Developing Melanocortin 3 Selective Ligands through C-Terminal Modification of Melanocortin Peptides . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/283606


University of Arizona

2. Hall, Sara M. Bradykinin Ligands and Receptors Involved in Neuropathic Pain .

Degree: 2015, University of Arizona

 Neuropathic pain is a prevalent disease with no effective, safe treatments and limited knowledge on the mechanisms involved. One target for neuropathic pain treatment may… (more)

Subjects/Keywords: neuropathic pain; non-opioid Dynorphin A; structure activity relationship; Biochemistry; bradykinin receptors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hall, S. M. (2015). Bradykinin Ligands and Receptors Involved in Neuropathic Pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/578606

Chicago Manual of Style (16th Edition):

Hall, Sara M. “Bradykinin Ligands and Receptors Involved in Neuropathic Pain .” 2015. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/578606.

MLA Handbook (7th Edition):

Hall, Sara M. “Bradykinin Ligands and Receptors Involved in Neuropathic Pain .” 2015. Web. 28 Nov 2020.

Vancouver:

Hall SM. Bradykinin Ligands and Receptors Involved in Neuropathic Pain . [Internet] [Doctoral dissertation]. University of Arizona; 2015. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/578606.

Council of Science Editors:

Hall SM. Bradykinin Ligands and Receptors Involved in Neuropathic Pain . [Doctoral Dissertation]. University of Arizona; 2015. Available from: http://hdl.handle.net/10150/578606


University of Arizona

3. Ramos-Colon, Cyf Nadine. Design, Synthesis, and Biological Evaluation of Novel Peptide Ligands as Kappa Opioid Receptor Antagonists .

Degree: 2016, University of Arizona

 Millions of people in the US currently suffer from chronic pain but available therapeutics do not provide effective chronic pain treatment. Opiate therapy is still… (more)

Subjects/Keywords: [Des-Arg7] Dynorphin A; Kappa Opioid Receptor Antagonist; Structure Activity Relationships; Pharmaceutical Sciences; Chronic Pain

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ramos-Colon, C. N. (2016). Design, Synthesis, and Biological Evaluation of Novel Peptide Ligands as Kappa Opioid Receptor Antagonists . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/621869

Chicago Manual of Style (16th Edition):

Ramos-Colon, Cyf Nadine. “Design, Synthesis, and Biological Evaluation of Novel Peptide Ligands as Kappa Opioid Receptor Antagonists .” 2016. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/621869.

MLA Handbook (7th Edition):

Ramos-Colon, Cyf Nadine. “Design, Synthesis, and Biological Evaluation of Novel Peptide Ligands as Kappa Opioid Receptor Antagonists .” 2016. Web. 28 Nov 2020.

Vancouver:

Ramos-Colon CN. Design, Synthesis, and Biological Evaluation of Novel Peptide Ligands as Kappa Opioid Receptor Antagonists . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/621869.

Council of Science Editors:

Ramos-Colon CN. Design, Synthesis, and Biological Evaluation of Novel Peptide Ligands as Kappa Opioid Receptor Antagonists . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/621869


University of Arizona

4. Remesic, Michael Vincent. The Design, Synthesis, and Biological Evaluation of Novel Peptidic Ligands for the Treatment of Chronic Neuropathic Pain .

Degree: 2017, University of Arizona

 Chronic neuropathic pain is a disease that impacts the livelihood of millions of people in the United States with no effective pain treatments and limited… (more)

Subjects/Keywords: Bivalent; Bradykinin; Chronic Pain; Multifunctional; Opioid; Peptide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Remesic, M. V. (2017). The Design, Synthesis, and Biological Evaluation of Novel Peptidic Ligands for the Treatment of Chronic Neuropathic Pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/625593

Chicago Manual of Style (16th Edition):

Remesic, Michael Vincent. “The Design, Synthesis, and Biological Evaluation of Novel Peptidic Ligands for the Treatment of Chronic Neuropathic Pain .” 2017. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/625593.

MLA Handbook (7th Edition):

Remesic, Michael Vincent. “The Design, Synthesis, and Biological Evaluation of Novel Peptidic Ligands for the Treatment of Chronic Neuropathic Pain .” 2017. Web. 28 Nov 2020.

Vancouver:

Remesic MV. The Design, Synthesis, and Biological Evaluation of Novel Peptidic Ligands for the Treatment of Chronic Neuropathic Pain . [Internet] [Doctoral dissertation]. University of Arizona; 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/625593.

Council of Science Editors:

Remesic MV. The Design, Synthesis, and Biological Evaluation of Novel Peptidic Ligands for the Treatment of Chronic Neuropathic Pain . [Doctoral Dissertation]. University of Arizona; 2017. Available from: http://hdl.handle.net/10150/625593


University of Arizona

5. Brabez, Nabila. Design, Synthesis and Study of Novel Multivalent Ligands - Toward New Markers of Cancer Cells .

Degree: 2012, University of Arizona

 Cancer is lacking early detection methods and treatment specificity. In order to increase the sensitivity and specificity towards cancer cells, we propose the use of… (more)

Subjects/Keywords: multivalent interactions; peptide dendrimers; scaffold; targeted therapy; Chemistry; cancer; GPCR

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Brabez, N. (2012). Design, Synthesis and Study of Novel Multivalent Ligands - Toward New Markers of Cancer Cells . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/238691

Chicago Manual of Style (16th Edition):

Brabez, Nabila. “Design, Synthesis and Study of Novel Multivalent Ligands - Toward New Markers of Cancer Cells .” 2012. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/238691.

MLA Handbook (7th Edition):

Brabez, Nabila. “Design, Synthesis and Study of Novel Multivalent Ligands - Toward New Markers of Cancer Cells .” 2012. Web. 28 Nov 2020.

Vancouver:

Brabez N. Design, Synthesis and Study of Novel Multivalent Ligands - Toward New Markers of Cancer Cells . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/238691.

Council of Science Editors:

Brabez N. Design, Synthesis and Study of Novel Multivalent Ligands - Toward New Markers of Cancer Cells . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/238691


University of Arizona

6. Olson, Keith Mathew. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .

Degree: 2017, University of Arizona

 Most clinical opioids produce analgesia through the Mu Opioid Receptor (MOR) providing the only effective treatment for chronic pain patients. These studies explore three pre-clinical… (more)

Subjects/Keywords: Bivalent; Delta Opioid Receptor; Functional Selectivity; MDOR Heterodimer; Mu Opioid Receptor; Opioid Signaling

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Olson, K. M. (2017). Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/626669

Chicago Manual of Style (16th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/626669.

MLA Handbook (7th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Web. 28 Nov 2020.

Vancouver:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Internet] [Doctoral dissertation]. University of Arizona; 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/626669.

Council of Science Editors:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Doctoral Dissertation]. University of Arizona; 2017. Available from: http://hdl.handle.net/10150/626669


University of Arizona

7. Nakath Gamlath Ralalage, Dayan Elshan. Targeting Melanocortin and Cholecystokinin Receptors via Multivalent Molecules Bearing Peptide Ligands .

Degree: 2014, University of Arizona

 Peptide receptor overexpression in diseased cells and tissues, including carcinomas provides an opportunity to develop therapeutics and imaging agents that selectively bind to such cells… (more)

Subjects/Keywords: Cholecystokinin; HEK293; Melanocortin; Multivalent; Time resolved fluorescence; Binding assay; Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nakath Gamlath Ralalage, D. E. (2014). Targeting Melanocortin and Cholecystokinin Receptors via Multivalent Molecules Bearing Peptide Ligands . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/338883

Chicago Manual of Style (16th Edition):

Nakath Gamlath Ralalage, Dayan Elshan. “Targeting Melanocortin and Cholecystokinin Receptors via Multivalent Molecules Bearing Peptide Ligands .” 2014. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/338883.

MLA Handbook (7th Edition):

Nakath Gamlath Ralalage, Dayan Elshan. “Targeting Melanocortin and Cholecystokinin Receptors via Multivalent Molecules Bearing Peptide Ligands .” 2014. Web. 28 Nov 2020.

Vancouver:

Nakath Gamlath Ralalage DE. Targeting Melanocortin and Cholecystokinin Receptors via Multivalent Molecules Bearing Peptide Ligands . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/338883.

Council of Science Editors:

Nakath Gamlath Ralalage DE. Targeting Melanocortin and Cholecystokinin Receptors via Multivalent Molecules Bearing Peptide Ligands . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/338883


University of Arizona

8. Khanal, Pitambar. Crystal Engineering with Piperazinediones .

Degree: 2016, University of Arizona

 Non covalent interactions are valuable tools for crystal engineering. Hydrogen bonding often plays a central role for molecular association among possible non covalent interactions. Together… (more)

Subjects/Keywords: Organic Synthesis; Piperazinediones; Chemistry; Crystal Engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Khanal, P. (2016). Crystal Engineering with Piperazinediones . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/612051

Chicago Manual of Style (16th Edition):

Khanal, Pitambar. “Crystal Engineering with Piperazinediones .” 2016. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/612051.

MLA Handbook (7th Edition):

Khanal, Pitambar. “Crystal Engineering with Piperazinediones .” 2016. Web. 28 Nov 2020.

Vancouver:

Khanal P. Crystal Engineering with Piperazinediones . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/612051.

Council of Science Editors:

Khanal P. Crystal Engineering with Piperazinediones . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/612051


University of Arizona

9. Castillo-Montoya, Javier. Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction .

Degree: 2016, University of Arizona

 The function of most proteins is regulated by post-translational modifications, of which phosphorylation in particular has been shown to be ubiquitous and of paramount importance… (more)

Subjects/Keywords: Kinases; Ligand-Gated Phosphorylation; Protein Engineering; Split-Kinase; Split-Phosphatase; Chemical Inducer of Dimerization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Castillo-Montoya, J. (2016). Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/623179

Chicago Manual of Style (16th Edition):

Castillo-Montoya, Javier. “Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction .” 2016. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/623179.

MLA Handbook (7th Edition):

Castillo-Montoya, Javier. “Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction .” 2016. Web. 28 Nov 2020.

Vancouver:

Castillo-Montoya J. Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/623179.

Council of Science Editors:

Castillo-Montoya J. Development of Orthogonal Split-Kinase and Split-Phosphatase Systems for Interrogating and Rewiring Signal Transduction . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/623179


University of Arizona

10. Zhou, Yang. Development of Selective Peptide Ligands Targeting Melanocortin Receptors for Melanoma Prevention and Therapy .

Degree: 2019, University of Arizona

 Melanocortin receptors are a family of G-protein-coupled receptors (GPCRs) that regulate many important physiological functions. Specifically, melanocortin-1-receptor (MC1R) on skin melanocytes regulates skin pigmentation, which… (more)

Subjects/Keywords: MC1R; melanocortin-1-receptor; melanoma; oral availability; peptide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhou, Y. (2019). Development of Selective Peptide Ligands Targeting Melanocortin Receptors for Melanoma Prevention and Therapy . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/631955

Chicago Manual of Style (16th Edition):

Zhou, Yang. “Development of Selective Peptide Ligands Targeting Melanocortin Receptors for Melanoma Prevention and Therapy .” 2019. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/631955.

MLA Handbook (7th Edition):

Zhou, Yang. “Development of Selective Peptide Ligands Targeting Melanocortin Receptors for Melanoma Prevention and Therapy .” 2019. Web. 28 Nov 2020.

Vancouver:

Zhou Y. Development of Selective Peptide Ligands Targeting Melanocortin Receptors for Melanoma Prevention and Therapy . [Internet] [Doctoral dissertation]. University of Arizona; 2019. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/631955.

Council of Science Editors:

Zhou Y. Development of Selective Peptide Ligands Targeting Melanocortin Receptors for Melanoma Prevention and Therapy . [Doctoral Dissertation]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/631955


University of Arizona

11. LI, YINGXUE. DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN .

Degree: 2011, University of Arizona

 Structure-activity relationships (SAR) of opioid peptide analogues related to endorphin or dynorphin have provided rational and powerful approaches toward the design of peptide therapeutics. A… (more)

Subjects/Keywords: Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

LI, Y. (2011). DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/203033

Chicago Manual of Style (16th Edition):

LI, YINGXUE. “DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN .” 2011. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/203033.

MLA Handbook (7th Edition):

LI, YINGXUE. “DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN .” 2011. Web. 28 Nov 2020.

Vancouver:

LI Y. DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/203033.

Council of Science Editors:

LI Y. DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/203033


University of Arizona

12. Shekhawat, Sujan Singh. Genetically Encoded Sensors for Detection of Proteases Utilizing Auto-Inhibited Coiled Coils and Split-Protein Reassembly .

Degree: 2011, University of Arizona

 The detection of cellular events is central to understanding biomoleculer processes as well as aid in therapeutic intervention strategies. One of the most fascinating biomoleculer… (more)

Subjects/Keywords: Protease; Split Protein Reassembly; Chemistry; Casapse; Coiled Coils

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shekhawat, S. S. (2011). Genetically Encoded Sensors for Detection of Proteases Utilizing Auto-Inhibited Coiled Coils and Split-Protein Reassembly . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/205209

Chicago Manual of Style (16th Edition):

Shekhawat, Sujan Singh. “Genetically Encoded Sensors for Detection of Proteases Utilizing Auto-Inhibited Coiled Coils and Split-Protein Reassembly .” 2011. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/205209.

MLA Handbook (7th Edition):

Shekhawat, Sujan Singh. “Genetically Encoded Sensors for Detection of Proteases Utilizing Auto-Inhibited Coiled Coils and Split-Protein Reassembly .” 2011. Web. 28 Nov 2020.

Vancouver:

Shekhawat SS. Genetically Encoded Sensors for Detection of Proteases Utilizing Auto-Inhibited Coiled Coils and Split-Protein Reassembly . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/205209.

Council of Science Editors:

Shekhawat SS. Genetically Encoded Sensors for Detection of Proteases Utilizing Auto-Inhibited Coiled Coils and Split-Protein Reassembly . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/205209


University of Arizona

13. Shen, Shengyi. Development of Split-protein Systems for Interrogating Biomacromolecules .

Degree: 2013, University of Arizona

 The specific interactions of macromolecules along with the activity of enzymes are central to all aspects of biology. It is well recognized that when the… (more)

Subjects/Keywords: Poly (ADP-ribose); protein kinase; Quantum Dot; split-protein; Chemistry; chemically induced dimerization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shen, S. (2013). Development of Split-protein Systems for Interrogating Biomacromolecules . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/308885

Chicago Manual of Style (16th Edition):

Shen, Shengyi. “Development of Split-protein Systems for Interrogating Biomacromolecules .” 2013. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/308885.

MLA Handbook (7th Edition):

Shen, Shengyi. “Development of Split-protein Systems for Interrogating Biomacromolecules .” 2013. Web. 28 Nov 2020.

Vancouver:

Shen S. Development of Split-protein Systems for Interrogating Biomacromolecules . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/308885.

Council of Science Editors:

Shen S. Development of Split-protein Systems for Interrogating Biomacromolecules . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/308885


University of Arizona

14. Skinner, David P. Hormone Induced "Migraine" and Attempts at Blocking Opiate Reward through NK1 .

Degree: 2014, University of Arizona

 Migraine headache is one of the most common neurological disorders. While the mechanisms contributing to migraine pathophysiology have yet to be fully elucidated, the disproportionate… (more)

Subjects/Keywords: Headache; Migraine; Neurokinin; Medical Pharmacology; Estradiol

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Skinner, D. P. (2014). Hormone Induced "Migraine" and Attempts at Blocking Opiate Reward through NK1 . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/321547

Chicago Manual of Style (16th Edition):

Skinner, David P. “Hormone Induced "Migraine" and Attempts at Blocking Opiate Reward through NK1 .” 2014. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/321547.

MLA Handbook (7th Edition):

Skinner, David P. “Hormone Induced "Migraine" and Attempts at Blocking Opiate Reward through NK1 .” 2014. Web. 28 Nov 2020.

Vancouver:

Skinner DP. Hormone Induced "Migraine" and Attempts at Blocking Opiate Reward through NK1 . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/321547.

Council of Science Editors:

Skinner DP. Hormone Induced "Migraine" and Attempts at Blocking Opiate Reward through NK1 . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/321547


University of Arizona

15. Anglin, Bobbi Lynn. Design and Synthesis of PACAP Based Glycopeptide Analogs; Effects of Glycosylation on Activity and Blood-Brain Barrier Penetration .

Degree: 2014, University of Arizona

 The incidence of neurodegenerative disorders like Parkinson’s disease (PD) and Alzheimer’s disease (AD) are increasing as the population ages. Slowing the rate of neurological decline… (more)

Subjects/Keywords: neuroprotection; PAC1R; PACAP; Parkinson's disease; Pharmaceutical Sciences; glycopeptide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Anglin, B. L. (2014). Design and Synthesis of PACAP Based Glycopeptide Analogs; Effects of Glycosylation on Activity and Blood-Brain Barrier Penetration . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/321595

Chicago Manual of Style (16th Edition):

Anglin, Bobbi Lynn. “Design and Synthesis of PACAP Based Glycopeptide Analogs; Effects of Glycosylation on Activity and Blood-Brain Barrier Penetration .” 2014. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/321595.

MLA Handbook (7th Edition):

Anglin, Bobbi Lynn. “Design and Synthesis of PACAP Based Glycopeptide Analogs; Effects of Glycosylation on Activity and Blood-Brain Barrier Penetration .” 2014. Web. 28 Nov 2020.

Vancouver:

Anglin BL. Design and Synthesis of PACAP Based Glycopeptide Analogs; Effects of Glycosylation on Activity and Blood-Brain Barrier Penetration . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/321595.

Council of Science Editors:

Anglin BL. Design and Synthesis of PACAP Based Glycopeptide Analogs; Effects of Glycosylation on Activity and Blood-Brain Barrier Penetration . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/321595


University of Arizona

16. Dehigaspitiya, Dilani Chathurika. Design, Synthesis, And Testing Of Multivalent Compounds Targeted To Melanocortin Receptors .

Degree: 2014, University of Arizona

 The early detection and successful treatment of many human cancers would be facilitated by the availability of reagents that could seek out and selectively bind… (more)

Subjects/Keywords: Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dehigaspitiya, D. C. (2014). Design, Synthesis, And Testing Of Multivalent Compounds Targeted To Melanocortin Receptors . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/332660

Chicago Manual of Style (16th Edition):

Dehigaspitiya, Dilani Chathurika. “Design, Synthesis, And Testing Of Multivalent Compounds Targeted To Melanocortin Receptors .” 2014. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/332660.

MLA Handbook (7th Edition):

Dehigaspitiya, Dilani Chathurika. “Design, Synthesis, And Testing Of Multivalent Compounds Targeted To Melanocortin Receptors .” 2014. Web. 28 Nov 2020.

Vancouver:

Dehigaspitiya DC. Design, Synthesis, And Testing Of Multivalent Compounds Targeted To Melanocortin Receptors . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/332660.

Council of Science Editors:

Dehigaspitiya DC. Design, Synthesis, And Testing Of Multivalent Compounds Targeted To Melanocortin Receptors . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/332660

17. Kulkarni, Vinod V. Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands .

Degree: 2012, University of Arizona

 Biologically many disease states lead to changes in expressed proteins. Therefore, "system changes" that occur must be considered in any treatment for the disease. This… (more)

Subjects/Keywords: microwave; opioid; peptide cyclization; Chemistry; bifunctional ligands; melanocortin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kulkarni, V. V. (2012). Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/228191

Chicago Manual of Style (16th Edition):

Kulkarni, Vinod V. “Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands .” 2012. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/228191.

MLA Handbook (7th Edition):

Kulkarni, Vinod V. “Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands .” 2012. Web. 28 Nov 2020.

Vancouver:

Kulkarni VV. Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/228191.

Council of Science Editors:

Kulkarni VV. Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/228191


University of Arizona

18. Andrus, Danice M. The design and synthesis of imine-bridged cyclic peptides andthe solid phase synthesis of β-turn mimetics.

Degree: 2004, University of Arizona

 Pain is perhaps the most unpleasant sensation humans experience. While pain is important in preventing further injury and as a detection mechanism for ill-health; effective… (more)

Subjects/Keywords: Chemistry; Organic.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Andrus, D. M. (2004). The design and synthesis of imine-bridged cyclic peptides andthe solid phase synthesis of β-turn mimetics. (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/291597

Chicago Manual of Style (16th Edition):

Andrus, Danice M. “The design and synthesis of imine-bridged cyclic peptides andthe solid phase synthesis of β-turn mimetics.” 2004. Masters Thesis, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/291597.

MLA Handbook (7th Edition):

Andrus, Danice M. “The design and synthesis of imine-bridged cyclic peptides andthe solid phase synthesis of β-turn mimetics.” 2004. Web. 28 Nov 2020.

Vancouver:

Andrus DM. The design and synthesis of imine-bridged cyclic peptides andthe solid phase synthesis of β-turn mimetics. [Internet] [Masters thesis]. University of Arizona; 2004. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/291597.

Council of Science Editors:

Andrus DM. The design and synthesis of imine-bridged cyclic peptides andthe solid phase synthesis of β-turn mimetics. [Masters Thesis]. University of Arizona; 2004. Available from: http://hdl.handle.net/10150/291597


University of Arizona

19. Cavagnero, Silvia, 1962-. Structure-activity studies of delta-selective opioid analogues .

Degree: 1990, University of Arizona

 The two structurally different peptides DPDPE and Dermenkephalin show a similar remarkably high affinity and selectivity for the delta opioid receptor subtype. An effort has… (more)

Subjects/Keywords: Chemistry, Biochemistry.; Chemistry, Organic.; Chemistry, Pharmaceutical.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cavagnero, Silvia, 1. (1990). Structure-activity studies of delta-selective opioid analogues . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/278183

Chicago Manual of Style (16th Edition):

Cavagnero, Silvia, 1962-. “Structure-activity studies of delta-selective opioid analogues .” 1990. Masters Thesis, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/278183.

MLA Handbook (7th Edition):

Cavagnero, Silvia, 1962-. “Structure-activity studies of delta-selective opioid analogues .” 1990. Web. 28 Nov 2020.

Vancouver:

Cavagnero, Silvia 1. Structure-activity studies of delta-selective opioid analogues . [Internet] [Masters thesis]. University of Arizona; 1990. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/278183.

Council of Science Editors:

Cavagnero, Silvia 1. Structure-activity studies of delta-selective opioid analogues . [Masters Thesis]. University of Arizona; 1990. Available from: http://hdl.handle.net/10150/278183


University of Arizona

20. Ferguson, Ronald Dale, 1966-. Design, synthesis and biological screening of combinatorial chemical libraries .

Degree: 1996, University of Arizona

 Although combinatorial libraries owe their inception to applications in peptide and bacteriophage libraries, the breadth of current applications include solution phase chemical reaction optimization, material… (more)

Subjects/Keywords: Chemistry, Biochemistry.; Chemistry, Organic.; Chemistry, Pharmaceutical.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ferguson, Ronald Dale, 1. (1996). Design, synthesis and biological screening of combinatorial chemical libraries . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/278584

Chicago Manual of Style (16th Edition):

Ferguson, Ronald Dale, 1966-. “Design, synthesis and biological screening of combinatorial chemical libraries .” 1996. Masters Thesis, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/278584.

MLA Handbook (7th Edition):

Ferguson, Ronald Dale, 1966-. “Design, synthesis and biological screening of combinatorial chemical libraries .” 1996. Web. 28 Nov 2020.

Vancouver:

Ferguson, Ronald Dale 1. Design, synthesis and biological screening of combinatorial chemical libraries . [Internet] [Masters thesis]. University of Arizona; 1996. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/278584.

Council of Science Editors:

Ferguson, Ronald Dale 1. Design, synthesis and biological screening of combinatorial chemical libraries . [Masters Thesis]. University of Arizona; 1996. Available from: http://hdl.handle.net/10150/278584


University of Arizona

21. Liao, Subo, 1963-. Design and synthesis of topographically constrained amino acids, and bioactive peptides for studies of ligand-receptor interaction, and for de novo design of delta-opioid selective non-peptide mimetics as potential therapeutics .

Degree: 1997, University of Arizona

 Topographical constraint is the most powerful approach for the design of bioactive peptides to explore the bioactive conformation of crucial side-chain pharmacophores of amino acid… (more)

Subjects/Keywords: Chemistry, Organic.; Chemistry, Pharmaceutical.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Liao, Subo, 1. (1997). Design and synthesis of topographically constrained amino acids, and bioactive peptides for studies of ligand-receptor interaction, and for de novo design of delta-opioid selective non-peptide mimetics as potential therapeutics . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/282418

Chicago Manual of Style (16th Edition):

Liao, Subo, 1963-. “Design and synthesis of topographically constrained amino acids, and bioactive peptides for studies of ligand-receptor interaction, and for de novo design of delta-opioid selective non-peptide mimetics as potential therapeutics .” 1997. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/282418.

MLA Handbook (7th Edition):

Liao, Subo, 1963-. “Design and synthesis of topographically constrained amino acids, and bioactive peptides for studies of ligand-receptor interaction, and for de novo design of delta-opioid selective non-peptide mimetics as potential therapeutics .” 1997. Web. 28 Nov 2020.

Vancouver:

Liao, Subo 1. Design and synthesis of topographically constrained amino acids, and bioactive peptides for studies of ligand-receptor interaction, and for de novo design of delta-opioid selective non-peptide mimetics as potential therapeutics . [Internet] [Doctoral dissertation]. University of Arizona; 1997. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/282418.

Council of Science Editors:

Liao, Subo 1. Design and synthesis of topographically constrained amino acids, and bioactive peptides for studies of ligand-receptor interaction, and for de novo design of delta-opioid selective non-peptide mimetics as potential therapeutics . [Doctoral Dissertation]. University of Arizona; 1997. Available from: http://hdl.handle.net/10150/282418


University of Arizona

22. Han, Guoxia. Design, synthesis, pharmacology, and structural analysis of bioactive melanocortin receptors' ligands by hybrid approaches .

Degree: 2000, University of Arizona

 A number of alpha-melanotropin (α-MSH) analogues have been designed de novo, synthesized and bioassayed at different melanocortin receptors from frog skins, mice and humans. These… (more)

Subjects/Keywords: Chemistry, Biochemistry.; Chemistry, Pharmaceutical.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Han, G. (2000). Design, synthesis, pharmacology, and structural analysis of bioactive melanocortin receptors' ligands by hybrid approaches . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/284287

Chicago Manual of Style (16th Edition):

Han, Guoxia. “Design, synthesis, pharmacology, and structural analysis of bioactive melanocortin receptors' ligands by hybrid approaches .” 2000. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/284287.

MLA Handbook (7th Edition):

Han, Guoxia. “Design, synthesis, pharmacology, and structural analysis of bioactive melanocortin receptors' ligands by hybrid approaches .” 2000. Web. 28 Nov 2020.

Vancouver:

Han G. Design, synthesis, pharmacology, and structural analysis of bioactive melanocortin receptors' ligands by hybrid approaches . [Internet] [Doctoral dissertation]. University of Arizona; 2000. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/284287.

Council of Science Editors:

Han G. Design, synthesis, pharmacology, and structural analysis of bioactive melanocortin receptors' ligands by hybrid approaches . [Doctoral Dissertation]. University of Arizona; 2000. Available from: http://hdl.handle.net/10150/284287


University of Arizona

23. Ahn, Jung-Mo. Search for bioactive conformation of glucagon and development of potent glucagon antagonists .

Degree: 2000, University of Arizona

 In pursuit of the working model of how glucagon interacts with the glucagon receptor and how glucagon antagonists exert their different activities, 42 glucagon analogues… (more)

Subjects/Keywords: Chemistry; Organic.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ahn, J. (2000). Search for bioactive conformation of glucagon and development of potent glucagon antagonists . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/284301

Chicago Manual of Style (16th Edition):

Ahn, Jung-Mo. “Search for bioactive conformation of glucagon and development of potent glucagon antagonists .” 2000. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/284301.

MLA Handbook (7th Edition):

Ahn, Jung-Mo. “Search for bioactive conformation of glucagon and development of potent glucagon antagonists .” 2000. Web. 28 Nov 2020.

Vancouver:

Ahn J. Search for bioactive conformation of glucagon and development of potent glucagon antagonists . [Internet] [Doctoral dissertation]. University of Arizona; 2000. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/284301.

Council of Science Editors:

Ahn J. Search for bioactive conformation of glucagon and development of potent glucagon antagonists . [Doctoral Dissertation]. University of Arizona; 2000. Available from: http://hdl.handle.net/10150/284301


University of Arizona

24. Alfaro-Lopez, Lorenzo Josue. Development of new conformationally and topographically constrained p60(c-src) PTK inhibitors. Solution and solid-phase approaches for the synthesis of delta-opioid receptor peptidomimetic ligands .

Degree: 1999, University of Arizona

 Based on the efficient substrate for p60ᶜ⁻ˢʳᶜ protein tyrosine kinase (PTK) YIYGSFK (1) (K(m) = 55 μM) obtained by combinatorial methods, we have designed and… (more)

Subjects/Keywords: Chemistry, Organic.; Chemistry, Pharmaceutical.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Alfaro-Lopez, L. J. (1999). Development of new conformationally and topographically constrained p60(c-src) PTK inhibitors. Solution and solid-phase approaches for the synthesis of delta-opioid receptor peptidomimetic ligands . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/288981

Chicago Manual of Style (16th Edition):

Alfaro-Lopez, Lorenzo Josue. “Development of new conformationally and topographically constrained p60(c-src) PTK inhibitors. Solution and solid-phase approaches for the synthesis of delta-opioid receptor peptidomimetic ligands .” 1999. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/288981.

MLA Handbook (7th Edition):

Alfaro-Lopez, Lorenzo Josue. “Development of new conformationally and topographically constrained p60(c-src) PTK inhibitors. Solution and solid-phase approaches for the synthesis of delta-opioid receptor peptidomimetic ligands .” 1999. Web. 28 Nov 2020.

Vancouver:

Alfaro-Lopez LJ. Development of new conformationally and topographically constrained p60(c-src) PTK inhibitors. Solution and solid-phase approaches for the synthesis of delta-opioid receptor peptidomimetic ligands . [Internet] [Doctoral dissertation]. University of Arizona; 1999. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/288981.

Council of Science Editors:

Alfaro-Lopez LJ. Development of new conformationally and topographically constrained p60(c-src) PTK inhibitors. Solution and solid-phase approaches for the synthesis of delta-opioid receptor peptidomimetic ligands . [Doctoral Dissertation]. University of Arizona; 1999. Available from: http://hdl.handle.net/10150/288981


University of Arizona

25. Tang, Xue-jun. Asymmetric synthesis of stereochemically-defined and conformationally-constrained novel amino acids via direct alkylation of chiral nickel(II)-coordinated Schiff bases of glycine and alanine, and design and synthesis of selective peptide and non-peptide ligands for the delta-opioid receptor .

Degree: 2002, University of Arizona

 A systematic practical method to prepare highly chi (χ)-constrained amino acids has been developed. It was found that increasing the size of R¹ (see figure)… (more)

Subjects/Keywords: Health Sciences, Pharmacology.; Chemistry, Organic.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tang, X. (2002). Asymmetric synthesis of stereochemically-defined and conformationally-constrained novel amino acids via direct alkylation of chiral nickel(II)-coordinated Schiff bases of glycine and alanine, and design and synthesis of selective peptide and non-peptide ligands for the delta-opioid receptor . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/279911

Chicago Manual of Style (16th Edition):

Tang, Xue-jun. “Asymmetric synthesis of stereochemically-defined and conformationally-constrained novel amino acids via direct alkylation of chiral nickel(II)-coordinated Schiff bases of glycine and alanine, and design and synthesis of selective peptide and non-peptide ligands for the delta-opioid receptor .” 2002. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/279911.

MLA Handbook (7th Edition):

Tang, Xue-jun. “Asymmetric synthesis of stereochemically-defined and conformationally-constrained novel amino acids via direct alkylation of chiral nickel(II)-coordinated Schiff bases of glycine and alanine, and design and synthesis of selective peptide and non-peptide ligands for the delta-opioid receptor .” 2002. Web. 28 Nov 2020.

Vancouver:

Tang X. Asymmetric synthesis of stereochemically-defined and conformationally-constrained novel amino acids via direct alkylation of chiral nickel(II)-coordinated Schiff bases of glycine and alanine, and design and synthesis of selective peptide and non-peptide ligands for the delta-opioid receptor . [Internet] [Doctoral dissertation]. University of Arizona; 2002. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/279911.

Council of Science Editors:

Tang X. Asymmetric synthesis of stereochemically-defined and conformationally-constrained novel amino acids via direct alkylation of chiral nickel(II)-coordinated Schiff bases of glycine and alanine, and design and synthesis of selective peptide and non-peptide ligands for the delta-opioid receptor . [Doctoral Dissertation]. University of Arizona; 2002. Available from: http://hdl.handle.net/10150/279911


University of Arizona

26. Cai, Chaozhong. Asymmetric synthesis of chi-constrained pyroglutamic acids, glutamic acids and prolines for peptides and peptidomimetics .

Degree: 2001, University of Arizona

 The recent upsurge of interest in the peptide-based drug molecules has been accompanied by a great deal of attention to the design of stereochemically defined… (more)

Subjects/Keywords: Chemistry; Organic.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cai, C. (2001). Asymmetric synthesis of chi-constrained pyroglutamic acids, glutamic acids and prolines for peptides and peptidomimetics . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/280129

Chicago Manual of Style (16th Edition):

Cai, Chaozhong. “Asymmetric synthesis of chi-constrained pyroglutamic acids, glutamic acids and prolines for peptides and peptidomimetics .” 2001. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/280129.

MLA Handbook (7th Edition):

Cai, Chaozhong. “Asymmetric synthesis of chi-constrained pyroglutamic acids, glutamic acids and prolines for peptides and peptidomimetics .” 2001. Web. 28 Nov 2020.

Vancouver:

Cai C. Asymmetric synthesis of chi-constrained pyroglutamic acids, glutamic acids and prolines for peptides and peptidomimetics . [Internet] [Doctoral dissertation]. University of Arizona; 2001. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/280129.

Council of Science Editors:

Cai C. Asymmetric synthesis of chi-constrained pyroglutamic acids, glutamic acids and prolines for peptides and peptidomimetics . [Doctoral Dissertation]. University of Arizona; 2001. Available from: http://hdl.handle.net/10150/280129


University of Arizona

27. Agnes, Richard S. New paradigm for drug design: Design and synthesis of novel biologically active peptides that are agonists at opioid receptors and antagonists at cholecystokinin receptors .

Degree: 2003, University of Arizona

 We now know from genomics that many disease states lead to changes in expressed proteins (adaptation/plasticity). Therefore, drug design and discovery based on normal states… (more)

Subjects/Keywords: Chemistry; Pharmaceutical.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Agnes, R. S. (2003). New paradigm for drug design: Design and synthesis of novel biologically active peptides that are agonists at opioid receptors and antagonists at cholecystokinin receptors . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/280340

Chicago Manual of Style (16th Edition):

Agnes, Richard S. “New paradigm for drug design: Design and synthesis of novel biologically active peptides that are agonists at opioid receptors and antagonists at cholecystokinin receptors .” 2003. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/280340.

MLA Handbook (7th Edition):

Agnes, Richard S. “New paradigm for drug design: Design and synthesis of novel biologically active peptides that are agonists at opioid receptors and antagonists at cholecystokinin receptors .” 2003. Web. 28 Nov 2020.

Vancouver:

Agnes RS. New paradigm for drug design: Design and synthesis of novel biologically active peptides that are agonists at opioid receptors and antagonists at cholecystokinin receptors . [Internet] [Doctoral dissertation]. University of Arizona; 2003. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/280340.

Council of Science Editors:

Agnes RS. New paradigm for drug design: Design and synthesis of novel biologically active peptides that are agonists at opioid receptors and antagonists at cholecystokinin receptors . [Doctoral Dissertation]. University of Arizona; 2003. Available from: http://hdl.handle.net/10150/280340


University of Arizona

28. Xiong, Chiyi. Asymmetric synthesis of conformationally and topographically constrained amino acids as peptidomimetics: An approach to design and synthesis of opioid receptor selective ligands .

Degree: 2003, University of Arizona

 As part of continuing efforts to obtain backbone and side chain conformationally constrained, novel amino acids,¹⁻⁷ we have successfully developed the asymmetric synthesis of β-phenyl-substituted… (more)

Subjects/Keywords: Health Sciences, Pharmacology.; Chemistry, Biochemistry.; Chemistry, Organic.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xiong, C. (2003). Asymmetric synthesis of conformationally and topographically constrained amino acids as peptidomimetics: An approach to design and synthesis of opioid receptor selective ligands . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/280393

Chicago Manual of Style (16th Edition):

Xiong, Chiyi. “Asymmetric synthesis of conformationally and topographically constrained amino acids as peptidomimetics: An approach to design and synthesis of opioid receptor selective ligands .” 2003. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/280393.

MLA Handbook (7th Edition):

Xiong, Chiyi. “Asymmetric synthesis of conformationally and topographically constrained amino acids as peptidomimetics: An approach to design and synthesis of opioid receptor selective ligands .” 2003. Web. 28 Nov 2020.

Vancouver:

Xiong C. Asymmetric synthesis of conformationally and topographically constrained amino acids as peptidomimetics: An approach to design and synthesis of opioid receptor selective ligands . [Internet] [Doctoral dissertation]. University of Arizona; 2003. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/280393.

Council of Science Editors:

Xiong C. Asymmetric synthesis of conformationally and topographically constrained amino acids as peptidomimetics: An approach to design and synthesis of opioid receptor selective ligands . [Doctoral Dissertation]. University of Arizona; 2003. Available from: http://hdl.handle.net/10150/280393


University of Arizona

29. Qiu, Wei. Design and synthesis of conformationally and topographically constrained amino acids as peptidomimetics .

Degree: 2001, University of Arizona

 A major goal of peptide research has been to elucidate or understand the relationships between a peptide's three-dimensional structure and its biological activity. De Novo… (more)

Subjects/Keywords: Chemistry, Biochemistry.; Chemistry, Organic.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Qiu, W. (2001). Design and synthesis of conformationally and topographically constrained amino acids as peptidomimetics . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/280486

Chicago Manual of Style (16th Edition):

Qiu, Wei. “Design and synthesis of conformationally and topographically constrained amino acids as peptidomimetics .” 2001. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/280486.

MLA Handbook (7th Edition):

Qiu, Wei. “Design and synthesis of conformationally and topographically constrained amino acids as peptidomimetics .” 2001. Web. 28 Nov 2020.

Vancouver:

Qiu W. Design and synthesis of conformationally and topographically constrained amino acids as peptidomimetics . [Internet] [Doctoral dissertation]. University of Arizona; 2001. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/280486.

Council of Science Editors:

Qiu W. Design and synthesis of conformationally and topographically constrained amino acids as peptidomimetics . [Doctoral Dissertation]. University of Arizona; 2001. Available from: http://hdl.handle.net/10150/280486


University of Arizona

30. Stankova, Magdalena. Design and synthesis of novel melanocortin receptor ligands .

Degree: 2004, University of Arizona

 Melanocortin receptors (MC1R-MC5R) belong to the G-protein coupled receptor superfamily. The interactions of peptide hormones (ACTH, alpha-, beta- and gamma-MSH) with the melanocortin receptors regulate… (more)

Subjects/Keywords: Chemistry; Organic.

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Stankova, M. (2004). Design and synthesis of novel melanocortin receptor ligands . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/280536

Chicago Manual of Style (16th Edition):

Stankova, Magdalena. “Design and synthesis of novel melanocortin receptor ligands .” 2004. Doctoral Dissertation, University of Arizona. Accessed November 28, 2020. http://hdl.handle.net/10150/280536.

MLA Handbook (7th Edition):

Stankova, Magdalena. “Design and synthesis of novel melanocortin receptor ligands .” 2004. Web. 28 Nov 2020.

Vancouver:

Stankova M. Design and synthesis of novel melanocortin receptor ligands . [Internet] [Doctoral dissertation]. University of Arizona; 2004. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10150/280536.

Council of Science Editors:

Stankova M. Design and synthesis of novel melanocortin receptor ligands . [Doctoral Dissertation]. University of Arizona; 2004. Available from: http://hdl.handle.net/10150/280536

[1] [2] [3]

.