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You searched for +publisher:"University of Notre Dame" +contributor:("Shahriar Mobashery, Committee Member"). Showing records 1 – 23 of 23 total matches.

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University of Notre Dame

1. Jeremiah J. Gassensmith. The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.

Degree: PhD, Chemistry and Biochemistry, 2009, University of Notre Dame

  Squaraine dyes are a unique class of near-infrared fluorophores that have fascinated researchers because of their interesting donor-acceptor structure and their electron deficient aromatic… (more)

Subjects/Keywords: Squaraine; Dyes; Chemistry; Supramolecular; Macrocycles; Probes; Anthracene

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APA (6th Edition):

Gassensmith, J. J. (2009). The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/jq085h75x57

Chicago Manual of Style (16th Edition):

Gassensmith, Jeremiah J.. “The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.” 2009. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/jq085h75x57.

MLA Handbook (7th Edition):

Gassensmith, Jeremiah J.. “The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>.” 2009. Web. 15 Jun 2019.

Vancouver:

Gassensmith JJ. The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/jq085h75x57.

Council of Science Editors:

Gassensmith JJ. The Supramolecular Chemistry of Squaraine Dyes and Anthracene Macrocycles</h1>. [Doctoral Dissertation]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/jq085h75x57


University of Notre Dame

2. Eve A. Granatosky. Biosynthetic Access to the GEX1A Scaffold: A Novel Therapeutic Approach for Niemann-Pick Type C Disease</h1>.

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

  GEX1A, alternatively known as herboxidiene, is a polyketide natural product isolated from Streptomyces chromofuscus that is known to target the spliceosome. Besides its reported… (more)

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APA (6th Edition):

Granatosky, E. A. (2018). Biosynthetic Access to the GEX1A Scaffold: A Novel Therapeutic Approach for Niemann-Pick Type C Disease</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/js956d59x83

Chicago Manual of Style (16th Edition):

Granatosky, Eve A.. “Biosynthetic Access to the GEX1A Scaffold: A Novel Therapeutic Approach for Niemann-Pick Type C Disease</h1>.” 2018. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/js956d59x83.

MLA Handbook (7th Edition):

Granatosky, Eve A.. “Biosynthetic Access to the GEX1A Scaffold: A Novel Therapeutic Approach for Niemann-Pick Type C Disease</h1>.” 2018. Web. 15 Jun 2019.

Vancouver:

Granatosky EA. Biosynthetic Access to the GEX1A Scaffold: A Novel Therapeutic Approach for Niemann-Pick Type C Disease</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2018. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/js956d59x83.

Council of Science Editors:

Granatosky EA. Biosynthetic Access to the GEX1A Scaffold: A Novel Therapeutic Approach for Niemann-Pick Type C Disease</h1>. [Doctoral Dissertation]. University of Notre Dame; 2018. Available from: https://curate.nd.edu/show/js956d59x83


University of Notre Dame

3. John Thomas Markiewicz. Development of a Vinylogous Horner-Wadsworth-Emmons Reagent: Syntheses of Siloxy Dienes, Aryl Amines and Medicinally Active Compounds</h1>.

Degree: PhD, Chemistry and Biochemistry, 2010, University of Notre Dame

  This thesis describes the progress on three different methodology projects and two multistep syntheses of a complex molecule. Specifically, we have synthesized a single… (more)

Subjects/Keywords: Vinylogout Horner-Wadsworth-Emmons; Niemann-Pick type C disease; siloxy dienes; Ullmann coupling; histone deacetylase inhibitor; trichostatin

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APA (6th Edition):

Markiewicz, J. T. (2010). Development of a Vinylogous Horner-Wadsworth-Emmons Reagent: Syntheses of Siloxy Dienes, Aryl Amines and Medicinally Active Compounds</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/qr46qz23722

Chicago Manual of Style (16th Edition):

Markiewicz, John Thomas. “Development of a Vinylogous Horner-Wadsworth-Emmons Reagent: Syntheses of Siloxy Dienes, Aryl Amines and Medicinally Active Compounds</h1>.” 2010. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/qr46qz23722.

MLA Handbook (7th Edition):

Markiewicz, John Thomas. “Development of a Vinylogous Horner-Wadsworth-Emmons Reagent: Syntheses of Siloxy Dienes, Aryl Amines and Medicinally Active Compounds</h1>.” 2010. Web. 15 Jun 2019.

Vancouver:

Markiewicz JT. Development of a Vinylogous Horner-Wadsworth-Emmons Reagent: Syntheses of Siloxy Dienes, Aryl Amines and Medicinally Active Compounds</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2010. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/qr46qz23722.

Council of Science Editors:

Markiewicz JT. Development of a Vinylogous Horner-Wadsworth-Emmons Reagent: Syntheses of Siloxy Dienes, Aryl Amines and Medicinally Active Compounds</h1>. [Doctoral Dissertation]. University of Notre Dame; 2010. Available from: https://curate.nd.edu/show/qr46qz23722


University of Notre Dame

4. Alexander Grant White. Selective Recognition of Bacteria Utilizing Zinc(II)-Dipicolylamine Conjugated Far-Red Fluorescent Probes</h1>.

Degree: PhD, Chemistry and Biochemistry, 2012, University of Notre Dame

  This dissertation evaluates a new family of near-infrared fluorescent molecular probes called squaraine rotaxanes for utility in whole animal imaging studies. Conjugating squaraine rotaxanes… (more)

Subjects/Keywords: chemiluminescence; zinc(II)-dipicolylamine; fluorescent probes; bacterial infection

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APA (6th Edition):

White, A. G. (2012). Selective Recognition of Bacteria Utilizing Zinc(II)-Dipicolylamine Conjugated Far-Red Fluorescent Probes</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/1r66j100r6v

Chicago Manual of Style (16th Edition):

White, Alexander Grant. “Selective Recognition of Bacteria Utilizing Zinc(II)-Dipicolylamine Conjugated Far-Red Fluorescent Probes</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/1r66j100r6v.

MLA Handbook (7th Edition):

White, Alexander Grant. “Selective Recognition of Bacteria Utilizing Zinc(II)-Dipicolylamine Conjugated Far-Red Fluorescent Probes</h1>.” 2012. Web. 15 Jun 2019.

Vancouver:

White AG. Selective Recognition of Bacteria Utilizing Zinc(II)-Dipicolylamine Conjugated Far-Red Fluorescent Probes</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/1r66j100r6v.

Council of Science Editors:

White AG. Selective Recognition of Bacteria Utilizing Zinc(II)-Dipicolylamine Conjugated Far-Red Fluorescent Probes</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/1r66j100r6v


University of Notre Dame

5. Ashley Elizabeth Ferraro. The Use of Computational Methods to Develop Selective Antagonists Targeting the Mammalian Notch1-Notch4 Homologs</h1>.

Degree: MS, Chemistry and Biochemistry, 2012, University of Notre Dame

  With the increasing strength of computational resources, computational drug design methodologies have been used as tools in the identification of lead molecules for drug… (more)

Subjects/Keywords: T-ALL; MM/PBSA; selectie binders; homology modeling; docking; molecular dynamics; SAHM; small molecule antagonists; peptide antagonists

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APA (6th Edition):

Ferraro, A. E. (2012). The Use of Computational Methods to Develop Selective Antagonists Targeting the Mammalian Notch1-Notch4 Homologs</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/5x21td98j1p

Chicago Manual of Style (16th Edition):

Ferraro, Ashley Elizabeth. “The Use of Computational Methods to Develop Selective Antagonists Targeting the Mammalian Notch1-Notch4 Homologs</h1>.” 2012. Masters Thesis, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/5x21td98j1p.

MLA Handbook (7th Edition):

Ferraro, Ashley Elizabeth. “The Use of Computational Methods to Develop Selective Antagonists Targeting the Mammalian Notch1-Notch4 Homologs</h1>.” 2012. Web. 15 Jun 2019.

Vancouver:

Ferraro AE. The Use of Computational Methods to Develop Selective Antagonists Targeting the Mammalian Notch1-Notch4 Homologs</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2012. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/5x21td98j1p.

Council of Science Editors:

Ferraro AE. The Use of Computational Methods to Develop Selective Antagonists Targeting the Mammalian Notch1-Notch4 Homologs</h1>. [Masters Thesis]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/5x21td98j1p


University of Notre Dame

6. Jennifer Laura Starner-Kreinbrink. Investigating beta-sheet folding and aggregation</h1>.

Degree: PhD, Chemistry and Biochemistry, 2015, University of Notre Dame

  Understanding how a polypeptide chain achieves its native fold and the complex interplay between folding and aggregation remains, even after over 40 years, an… (more)

Subjects/Keywords: cap structures; pertactin; beta-sheet; protein aggregation; protein folding; ropes; biomaterials

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APA (6th Edition):

Starner-Kreinbrink, J. L. (2015). Investigating beta-sheet folding and aggregation</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/pz50gt5705c

Chicago Manual of Style (16th Edition):

Starner-Kreinbrink, Jennifer Laura. “Investigating beta-sheet folding and aggregation</h1>.” 2015. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/pz50gt5705c.

MLA Handbook (7th Edition):

Starner-Kreinbrink, Jennifer Laura. “Investigating beta-sheet folding and aggregation</h1>.” 2015. Web. 15 Jun 2019.

Vancouver:

Starner-Kreinbrink JL. Investigating beta-sheet folding and aggregation</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2015. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/pz50gt5705c.

Council of Science Editors:

Starner-Kreinbrink JL. Investigating beta-sheet folding and aggregation</h1>. [Doctoral Dissertation]. University of Notre Dame; 2015. Available from: https://curate.nd.edu/show/pz50gt5705c


University of Notre Dame

7. Baiyuan Yang. New Synthetic Applications of Nitroso Diels-Alder and Ene Chemistry</h1>.

Degree: PhD, Chemistry and Biochemistry, 2010, University of Notre Dame

  The focus for this dissertation involved the development of new synthetic applications of nitroso Diels-Alder (NDA) reactions and nitroso ene reactions. Three projects have… (more)

Subjects/Keywords: Colchicine; Leucomycin; Ergosterol; Derivatization and Functionalization; Diels-Alder; Nitroso; Ene

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APA (6th Edition):

Yang, B. (2010). New Synthetic Applications of Nitroso Diels-Alder and Ene Chemistry</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/5t34sj15655

Chicago Manual of Style (16th Edition):

Yang, Baiyuan. “New Synthetic Applications of Nitroso Diels-Alder and Ene Chemistry</h1>.” 2010. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/5t34sj15655.

MLA Handbook (7th Edition):

Yang, Baiyuan. “New Synthetic Applications of Nitroso Diels-Alder and Ene Chemistry</h1>.” 2010. Web. 15 Jun 2019.

Vancouver:

Yang B. New Synthetic Applications of Nitroso Diels-Alder and Ene Chemistry</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2010. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/5t34sj15655.

Council of Science Editors:

Yang B. New Synthetic Applications of Nitroso Diels-Alder and Ene Chemistry</h1>. [Doctoral Dissertation]. University of Notre Dame; 2010. Available from: https://curate.nd.edu/show/5t34sj15655


University of Notre Dame

8. Kai Liu. Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>.

Degree: PhD, Chemistry and Biochemistry, 2009, University of Notre Dame

  Numerous polyketide natural products contain methyl ether functionality generated by either methoxymalonyl extender units or a selective O-methyl transferase associated with the polyketide synthase… (more)

Subjects/Keywords: ether transfer total synthesis

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APA (6th Edition):

Liu, K. (2009). Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/7h149p30z94

Chicago Manual of Style (16th Edition):

Liu, Kai. “Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>.” 2009. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/7h149p30z94.

MLA Handbook (7th Edition):

Liu, Kai. “Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>.” 2009. Web. 15 Jun 2019.

Vancouver:

Liu K. Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2009. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/7h149p30z94.

Council of Science Editors:

Liu K. Electrophile-Induced Ether Transfer and Application in Natural Product Total Synthesis</h1>. [Doctoral Dissertation]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/7h149p30z94


University of Notre Dame

9. Yao Shen. Applications of Atomistic Modeling in Drug Design</h1>.

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

  Structure based computer aided drug design has been proven as a potent tool in identifying lead molecules for drug targets, with the increasing number… (more)

Subjects/Keywords: notch; docking; molecular modeling; metabolic network; bromodomain; Drug design; MD

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APA (6th Edition):

Shen, Y. (2011). Applications of Atomistic Modeling in Drug Design</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/5q47rn31z3f

Chicago Manual of Style (16th Edition):

Shen, Yao. “Applications of Atomistic Modeling in Drug Design</h1>.” 2011. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/5q47rn31z3f.

MLA Handbook (7th Edition):

Shen, Yao. “Applications of Atomistic Modeling in Drug Design</h1>.” 2011. Web. 15 Jun 2019.

Vancouver:

Shen Y. Applications of Atomistic Modeling in Drug Design</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2011. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/5q47rn31z3f.

Council of Science Editors:

Shen Y. Applications of Atomistic Modeling in Drug Design</h1>. [Doctoral Dissertation]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/5q47rn31z3f


University of Notre Dame

10. John Herrington. Elucidation of the selection and roles of synonymous codons in protein biogenesis</h1>.

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

  In this thesis, the importance of rare codons on protein biogenesis as well as cell fitness will be discussed. To test the effects of… (more)

Subjects/Keywords: synonymous; protein folding; chloramphenicol acetyltransferase; protein biogenesis; continuous cell culture; codons; turbidostat

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APA (6th Edition):

Herrington, J. (2014). Elucidation of the selection and roles of synonymous codons in protein biogenesis</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/qf85n873d1n

Chicago Manual of Style (16th Edition):

Herrington, John. “Elucidation of the selection and roles of synonymous codons in protein biogenesis</h1>.” 2014. Masters Thesis, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/qf85n873d1n.

MLA Handbook (7th Edition):

Herrington, John. “Elucidation of the selection and roles of synonymous codons in protein biogenesis</h1>.” 2014. Web. 15 Jun 2019.

Vancouver:

Herrington J. Elucidation of the selection and roles of synonymous codons in protein biogenesis</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2014. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/qf85n873d1n.

Council of Science Editors:

Herrington J. Elucidation of the selection and roles of synonymous codons in protein biogenesis</h1>. [Masters Thesis]. University of Notre Dame; 2014. Available from: https://curate.nd.edu/show/qf85n873d1n


University of Notre Dame

11. Cheng Ji. Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>.

Degree: PhD, Chemistry and Biochemistry, 2012, University of Notre Dame

  Siderophores are an important class of natural products that have received wide attention for many years due to their unique properties as microbial iron… (more)

Subjects/Keywords: siderophore; antibiotics; linkers; drug-conjugate; pathogen detection

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APA (6th Edition):

Ji, C. (2012). Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/9w032229q13

Chicago Manual of Style (16th Edition):

Ji, Cheng. “Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/9w032229q13.

MLA Handbook (7th Edition):

Ji, Cheng. “Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>.” 2012. Web. 15 Jun 2019.

Vancouver:

Ji C. Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/9w032229q13.

Council of Science Editors:

Ji C. Exploiting Bacterial Iron Acquisition: From New Antibiotics to Pathogen Detection Devices</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/9w032229q13


University of Notre Dame

12. Lawrence P. Tardibono Jr. Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>.

Degree: PhD, Chemistry and Biochemistry, 2010, University of Notre Dame

  New methodologies were developed and used to synthesize novel benzodiazepines with anti-cancer activity and carbocyclic nucleosides. Appropriately functionalized acylnitroso-derived hetero-Diels-Alder cycloadducts were subjected to… (more)

Subjects/Keywords: organic synthesis; benzodiazepines; palladium allylation; nucleosides; nitroso; decarboxylation

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APA (6th Edition):

Jr., L. P. T. (2010). Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/h128nc60644

Chicago Manual of Style (16th Edition):

Jr., Lawrence P. Tardibono. “Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>.” 2010. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/h128nc60644.

MLA Handbook (7th Edition):

Jr., Lawrence P. Tardibono. “Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>.” 2010. Web. 15 Jun 2019.

Vancouver:

Jr. LPT. Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2010. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/h128nc60644.

Council of Science Editors:

Jr. LPT. Methodology Development and Syntheses of Biologically Relevant Molecules from Acylnitroso Cycloadducts: Access to Benzodiazepines and Carbocyclic Nucleosides</h1>. [Doctoral Dissertation]. University of Notre Dame; 2010. Available from: https://curate.nd.edu/show/h128nc60644


University of Notre Dame

13. Matthew Ryan Wilson. Synthesis, Conformational Analysis, and Biological Evaluation of the Potent Microtubule-Stabilizing Agents, (–)-Zampanolide and (–)-Dactylolide</h1>.

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

  Zampanolide, a 20-membered marine polyketide, exhibits low nanomolar cytotoxicity (0.25 – 3 ng/mL) against multiple human cancer cell lines and induces apoptosis through microtubule… (more)

Subjects/Keywords: polyketide; microtubule targeting agents; conformational analysis; synthesis

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APA (6th Edition):

Wilson, M. R. (2014). Synthesis, Conformational Analysis, and Biological Evaluation of the Potent Microtubule-Stabilizing Agents, (–)-Zampanolide and (–)-Dactylolide</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/tb09j388g0m

Chicago Manual of Style (16th Edition):

Wilson, Matthew Ryan. “Synthesis, Conformational Analysis, and Biological Evaluation of the Potent Microtubule-Stabilizing Agents, (–)-Zampanolide and (–)-Dactylolide</h1>.” 2014. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/tb09j388g0m.

MLA Handbook (7th Edition):

Wilson, Matthew Ryan. “Synthesis, Conformational Analysis, and Biological Evaluation of the Potent Microtubule-Stabilizing Agents, (–)-Zampanolide and (–)-Dactylolide</h1>.” 2014. Web. 15 Jun 2019.

Vancouver:

Wilson MR. Synthesis, Conformational Analysis, and Biological Evaluation of the Potent Microtubule-Stabilizing Agents, (–)-Zampanolide and (–)-Dactylolide</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2014. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/tb09j388g0m.

Council of Science Editors:

Wilson MR. Synthesis, Conformational Analysis, and Biological Evaluation of the Potent Microtubule-Stabilizing Agents, (–)-Zampanolide and (–)-Dactylolide</h1>. [Doctoral Dissertation]. University of Notre Dame; 2014. Available from: https://curate.nd.edu/show/tb09j388g0m


University of Notre Dame

14. Pauline Bourbon. Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>.

Degree: PhD, Chemistry and Biochemistry, 2012, University of Notre Dame

  This thesis describes our endeavors towards the development of therapeutic agents for Niemann-Pick type C disease (NPC), which is a rare, autosomal recessive lipid… (more)

Subjects/Keywords: Cholesterol; Caged compound; Niemann-Pick type C

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APA (6th Edition):

Bourbon, P. (2012). Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/0k225b01f5m

Chicago Manual of Style (16th Edition):

Bourbon, Pauline. “Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/0k225b01f5m.

MLA Handbook (7th Edition):

Bourbon, Pauline. “Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>.” 2012. Web. 15 Jun 2019.

Vancouver:

Bourbon P. Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/0k225b01f5m.

Council of Science Editors:

Bourbon P. Development of potential Niemann-Pick type C therapeutics and the synthesis of caged nicotinamide and cholesterol to gain a better understanding of cholesterol biosynthesis and trafficking</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/0k225b01f5m


University of Notre Dame

15. Lica Abu-Esba. Studies of Multivalent Probes as Bacterial Imaging Fluorophores and Agglutination Agents</h1>.

Degree: MS, Chemistry and Biochemistry, 2009, University of Notre Dame

  This study evaluates the performance of Bis-Zinc II dipicolylamine (ZnII-DPA) conjugated squaraine rotaxane as bacterial targeting probes. Firstly, binding assays with planktonic bacteria show… (more)

Subjects/Keywords: Squaraine Rotaxane; Multivalent probes; bacterial imaging agents; bacterial fluorophores; Agglutination agents

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APA (6th Edition):

Abu-Esba, L. (2009). Studies of Multivalent Probes as Bacterial Imaging Fluorophores and Agglutination Agents</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/t722h705695

Chicago Manual of Style (16th Edition):

Abu-Esba, Lica. “Studies of Multivalent Probes as Bacterial Imaging Fluorophores and Agglutination Agents</h1>.” 2009. Masters Thesis, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/t722h705695.

MLA Handbook (7th Edition):

Abu-Esba, Lica. “Studies of Multivalent Probes as Bacterial Imaging Fluorophores and Agglutination Agents</h1>.” 2009. Web. 15 Jun 2019.

Vancouver:

Abu-Esba L. Studies of Multivalent Probes as Bacterial Imaging Fluorophores and Agglutination Agents</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2009. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/t722h705695.

Council of Science Editors:

Abu-Esba L. Studies of Multivalent Probes as Bacterial Imaging Fluorophores and Agglutination Agents</h1>. [Masters Thesis]. University of Notre Dame; 2009. Available from: https://curate.nd.edu/show/t722h705695


University of Notre Dame

16. Edward J O'Neil. Synthesis and Study of Membrane Active Compounds</h1>.

Degree: PhD, Chemistry and Biochemistry, 2008, University of Notre Dame

  This dissertation describes the design, synthesis, and activity of molecules that interact specifically with vesicle or cellular membranes. The first section describes a series… (more)

Subjects/Keywords: cellular membrane; cellular delivery; phospholipid; bolaamphiphile; chloride transport; phosphatidylserine

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APA (6th Edition):

O'Neil, E. J. (2008). Synthesis and Study of Membrane Active Compounds</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/sb397655p2z

Chicago Manual of Style (16th Edition):

O'Neil, Edward J. “Synthesis and Study of Membrane Active Compounds</h1>.” 2008. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/sb397655p2z.

MLA Handbook (7th Edition):

O'Neil, Edward J. “Synthesis and Study of Membrane Active Compounds</h1>.” 2008. Web. 15 Jun 2019.

Vancouver:

O'Neil EJ. Synthesis and Study of Membrane Active Compounds</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2008. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/sb397655p2z.

Council of Science Editors:

O'Neil EJ. Synthesis and Study of Membrane Active Compounds</h1>. [Doctoral Dissertation]. University of Notre Dame; 2008. Available from: https://curate.nd.edu/show/sb397655p2z


University of Notre Dame

17. Choonkeun Kim. Aminoglycoside-Modifying Enzymes: Catalytic Mechanisms and Properties</h1>.

Degree: PhD, Chemistry and Biochemistry, 2006, University of Notre Dame

  Aminoglycoside 3’-phosphotransferases [APH(3’)s] are important bacterial resistance enzymes for aminoglycoside antibiotics. These enzymes transfer the phosphoryl group of ATP to the 3’-hydroxyl of the… (more)

Subjects/Keywords: ATPase; ordered bi-bi mechanism; kinetic mechanism; Theorell-Chance

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APA (6th Edition):

Kim, C. (2006). Aminoglycoside-Modifying Enzymes: Catalytic Mechanisms and Properties</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/dn39x061h4p

Chicago Manual of Style (16th Edition):

Kim, Choonkeun. “Aminoglycoside-Modifying Enzymes: Catalytic Mechanisms and Properties</h1>.” 2006. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/dn39x061h4p.

MLA Handbook (7th Edition):

Kim, Choonkeun. “Aminoglycoside-Modifying Enzymes: Catalytic Mechanisms and Properties</h1>.” 2006. Web. 15 Jun 2019.

Vancouver:

Kim C. Aminoglycoside-Modifying Enzymes: Catalytic Mechanisms and Properties</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2006. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/dn39x061h4p.

Council of Science Editors:

Kim C. Aminoglycoside-Modifying Enzymes: Catalytic Mechanisms and Properties</h1>. [Doctoral Dissertation]. University of Notre Dame; 2006. Available from: https://curate.nd.edu/show/dn39x061h4p


University of Notre Dame

18. Zhi Liang. Towards Precursor-Directed Biosynthesis and Synthesis of Myriaporone-Tedanolide Analogues</h1>.

Degree: MS, Chemistry and Biochemistry, 2006, University of Notre Dame

  This thesis details the synthetic progress towards the preparation of myriaporone-tedanolide analogues through novel precursor-directed biosynthesis as well as general organic synthesis. With the… (more)

Subjects/Keywords: MYRIAPORONE; PKS; PRECURSOR-DIRECTED; BIOSYNTHESIS; TEDANOLIDE

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APA (6th Edition):

Liang, Z. (2006). Towards Precursor-Directed Biosynthesis and Synthesis of Myriaporone-Tedanolide Analogues</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/c821gh95k6p

Chicago Manual of Style (16th Edition):

Liang, Zhi. “Towards Precursor-Directed Biosynthesis and Synthesis of Myriaporone-Tedanolide Analogues</h1>.” 2006. Masters Thesis, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/c821gh95k6p.

MLA Handbook (7th Edition):

Liang, Zhi. “Towards Precursor-Directed Biosynthesis and Synthesis of Myriaporone-Tedanolide Analogues</h1>.” 2006. Web. 15 Jun 2019.

Vancouver:

Liang Z. Towards Precursor-Directed Biosynthesis and Synthesis of Myriaporone-Tedanolide Analogues</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2006. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/c821gh95k6p.

Council of Science Editors:

Liang Z. Towards Precursor-Directed Biosynthesis and Synthesis of Myriaporone-Tedanolide Analogues</h1>. [Masters Thesis]. University of Notre Dame; 2006. Available from: https://curate.nd.edu/show/c821gh95k6p


University of Notre Dame

19. Myriam Patricia Roy. Structure-Activity Relationship of the Myriaporones and Biosynthetic Study of Tedanolide</h1>.

Degree: PhD, Chemistry and Biochemistry, 2008, University of Notre Dame

  The myriaporones and the tedanolides are two distinct classes of polyketide natural products that exhibit strong structural similarities as well as interesting antitumor activities.… (more)

Subjects/Keywords: myriaporone; structure-activity relationship; total synthesis; tedanolide; protein synthesis inhibitor

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APA (6th Edition):

Roy, M. P. (2008). Structure-Activity Relationship of the Myriaporones and Biosynthetic Study of Tedanolide</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/02870v85201

Chicago Manual of Style (16th Edition):

Roy, Myriam Patricia. “Structure-Activity Relationship of the Myriaporones and Biosynthetic Study of Tedanolide</h1>.” 2008. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/02870v85201.

MLA Handbook (7th Edition):

Roy, Myriam Patricia. “Structure-Activity Relationship of the Myriaporones and Biosynthetic Study of Tedanolide</h1>.” 2008. Web. 15 Jun 2019.

Vancouver:

Roy MP. Structure-Activity Relationship of the Myriaporones and Biosynthetic Study of Tedanolide</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2008. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/02870v85201.

Council of Science Editors:

Roy MP. Structure-Activity Relationship of the Myriaporones and Biosynthetic Study of Tedanolide</h1>. [Doctoral Dissertation]. University of Notre Dame; 2008. Available from: https://curate.nd.edu/show/02870v85201


University of Notre Dame

20. Christopher B Harrison. Models and Mechanisms of DNA Damage Repair</h1>.

Degree: PhD, Chemistry and Biochemistry, 2007, University of Notre Dame

  Ultraviolet irradiation of DNA induces formation of two principal photoproducts, the more prevalent, less mutagenic cyclobutane pyrimidine dimer (CPD) and the less prevalent, more… (more)

Subjects/Keywords: DNA repair; oxetane; CPD; light-induced electron transfer; electron transfer; DNA photolyase; (6-4) photoproduct; DNA; CPD photolyase; carbinolamine; theozyme; (6-4) photolyase; radical anion; (6-4) Dewar; (6-4) oxetane; DNA damage; Thymine dimer; (6-4) dimer; cyclobutane pyrimidine dimer; photolyase; Dewar

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APA (6th Edition):

Harrison, C. B. (2007). Models and Mechanisms of DNA Damage Repair</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/hd76rx93b84

Chicago Manual of Style (16th Edition):

Harrison, Christopher B. “Models and Mechanisms of DNA Damage Repair</h1>.” 2007. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/hd76rx93b84.

MLA Handbook (7th Edition):

Harrison, Christopher B. “Models and Mechanisms of DNA Damage Repair</h1>.” 2007. Web. 15 Jun 2019.

Vancouver:

Harrison CB. Models and Mechanisms of DNA Damage Repair</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2007. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/hd76rx93b84.

Council of Science Editors:

Harrison CB. Models and Mechanisms of DNA Damage Repair</h1>. [Doctoral Dissertation]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/hd76rx93b84


University of Notre Dame

21. Jooyoung Cha. Penicillin-Binding Proteins in Pathogens: Characterizations of Catalytic Properties in Antibiotic Resistance</h1>.

Degree: PhD, Chemistry and Biochemistry, 2007, University of Notre Dame

  Treponema pallidum is the causative agent of syphilis and is exquisitely sensitive to penicillins and other §-lactam antibiotics. The Tp47, the novel 47 kDa… (more)

Subjects/Keywords: Regulatory protein BlaR1 and MecR1; beta-lactamase; lysine carboxylation; Tp47; Staphylococcus aureus; Penicillin-binding proteins

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APA (6th Edition):

Cha, J. (2007). Penicillin-Binding Proteins in Pathogens: Characterizations of Catalytic Properties in Antibiotic Resistance</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/df65v694x8k

Chicago Manual of Style (16th Edition):

Cha, Jooyoung. “Penicillin-Binding Proteins in Pathogens: Characterizations of Catalytic Properties in Antibiotic Resistance</h1>.” 2007. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/df65v694x8k.

MLA Handbook (7th Edition):

Cha, Jooyoung. “Penicillin-Binding Proteins in Pathogens: Characterizations of Catalytic Properties in Antibiotic Resistance</h1>.” 2007. Web. 15 Jun 2019.

Vancouver:

Cha J. Penicillin-Binding Proteins in Pathogens: Characterizations of Catalytic Properties in Antibiotic Resistance</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2007. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/df65v694x8k.

Council of Science Editors:

Cha J. Penicillin-Binding Proteins in Pathogens: Characterizations of Catalytic Properties in Antibiotic Resistance</h1>. [Doctoral Dissertation]. University of Notre Dame; 2007. Available from: https://curate.nd.edu/show/df65v694x8k


University of Notre Dame

22. Lauren L O'Neil. Base Flipping: Detection, Structures and Energetics</h1>.

Degree: PhD, Chemistry and Biochemistry, 2008, University of Notre Dame

  Base flipping is the movement of a DNA base from an intrahelical, base stacked position to an extrahelical, solvent exposed position. As there are… (more)

Subjects/Keywords: potential of mean force; base flipping; molecular dynamics; DNA; fluorescence detection

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APA (6th Edition):

O'Neil, L. L. (2008). Base Flipping: Detection, Structures and Energetics</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/9306sx63d8n

Chicago Manual of Style (16th Edition):

O'Neil, Lauren L. “Base Flipping: Detection, Structures and Energetics</h1>.” 2008. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/9306sx63d8n.

MLA Handbook (7th Edition):

O'Neil, Lauren L. “Base Flipping: Detection, Structures and Energetics</h1>.” 2008. Web. 15 Jun 2019.

Vancouver:

O'Neil LL. Base Flipping: Detection, Structures and Energetics</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2008. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/9306sx63d8n.

Council of Science Editors:

O'Neil LL. Base Flipping: Detection, Structures and Energetics</h1>. [Doctoral Dissertation]. University of Notre Dame; 2008. Available from: https://curate.nd.edu/show/9306sx63d8n


University of Notre Dame

23. Roger G. Hanshaw. Small Molecules for the Selective Recognition of Biomembrane Components</h1>.

Degree: PhD, Chemistry and Biochemistry, 2006, University of Notre Dame

  This dissertation describes the design and evaluation of small molecules that interact specifically with certain components of the cell plasma membrane surface and interior.… (more)

Subjects/Keywords: molecular recognition; dipicolylamine; apoptosis; phosphatidylserine

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APA (6th Edition):

Hanshaw, R. G. (2006). Small Molecules for the Selective Recognition of Biomembrane Components</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/r781wd39m30

Chicago Manual of Style (16th Edition):

Hanshaw, Roger G.. “Small Molecules for the Selective Recognition of Biomembrane Components</h1>.” 2006. Doctoral Dissertation, University of Notre Dame. Accessed June 15, 2019. https://curate.nd.edu/show/r781wd39m30.

MLA Handbook (7th Edition):

Hanshaw, Roger G.. “Small Molecules for the Selective Recognition of Biomembrane Components</h1>.” 2006. Web. 15 Jun 2019.

Vancouver:

Hanshaw RG. Small Molecules for the Selective Recognition of Biomembrane Components</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2006. [cited 2019 Jun 15]. Available from: https://curate.nd.edu/show/r781wd39m30.

Council of Science Editors:

Hanshaw RG. Small Molecules for the Selective Recognition of Biomembrane Components</h1>. [Doctoral Dissertation]. University of Notre Dame; 2006. Available from: https://curate.nd.edu/show/r781wd39m30

.