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You searched for +publisher:"University of Michigan" +contributor:("Showalter, Hollis D."). Showing records 1 – 14 of 14 total matches.

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University of Michigan

1. Mady, Ahmed. Development and Characterization of Novel Mcl-1 Inhibitors for Treatment of Cancer.

Degree: PhD, Medicinal Chemistry, 2016, University of Michigan

 Myeloid cell leukemia-1 (Mcl-1) is a potent anti-apoptotic protein, member of the anti-apoptotic Bcl-2 family. Overexpression of Mcl-1 is associated with high tumor grade, resistance… (more)

Subjects/Keywords: small molecule Mcl-1 inhibitors; Pharmacy and Pharmacology; Health Sciences

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APA (6th Edition):

Mady, A. (2016). Development and Characterization of Novel Mcl-1 Inhibitors for Treatment of Cancer. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/135852

Chicago Manual of Style (16th Edition):

Mady, Ahmed. “Development and Characterization of Novel Mcl-1 Inhibitors for Treatment of Cancer.” 2016. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/135852.

MLA Handbook (7th Edition):

Mady, Ahmed. “Development and Characterization of Novel Mcl-1 Inhibitors for Treatment of Cancer.” 2016. Web. 26 Jun 2019.

Vancouver:

Mady A. Development and Characterization of Novel Mcl-1 Inhibitors for Treatment of Cancer. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/135852.

Council of Science Editors:

Mady A. Development and Characterization of Novel Mcl-1 Inhibitors for Treatment of Cancer. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/135852


University of Michigan

2. Abulwerdi, Fardokht Assadi. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.

Degree: PhD, Medicinal Chemistry, 2014, University of Michigan

 The mitochondrial pathway to apoptosis is regulated through the protein-protein interactions of pro- and anti-apoptotic members of Bcl-2 family proteins. Overexpression of the anti-apoptotic members… (more)

Subjects/Keywords: Anti-apoptotic Mcl-1; Medicinal Chemistry; Protein-protein Interaction Inhibitor; Cancer; Protein NMR Spectroscopy; Structure-activity Relationship; Biological Chemistry; Chemistry; Science

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APA (6th Edition):

Abulwerdi, F. A. (2014). Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107109

Chicago Manual of Style (16th Edition):

Abulwerdi, Fardokht Assadi. “Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/107109.

MLA Handbook (7th Edition):

Abulwerdi, Fardokht Assadi. “Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1.” 2014. Web. 26 Jun 2019.

Vancouver:

Abulwerdi FA. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/107109.

Council of Science Editors:

Abulwerdi FA. Structure-Based Design, Synthesis and Evaluation of Novel and Selective Small-Molecule Inhibitors of the Anti-Apoptotic Protein Mcl-1. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107109


University of Michigan

3. Danowitz, Amy Marie. I. Synthesizing and Identifying Small Molecule Probes for Targeting Transcriptional Co-factors II. Design and Implementation of a Peer-Led Practical Research Ethics Module for Teaching Graduate Research Ethics.

Degree: PhD, Chemistry, 2011, University of Michigan

 Activated transcription is a complex process that is governed by the interactions of several different proteins. As misregulation of transcription has been observed in many… (more)

Subjects/Keywords: Transcription; Allenamides; Ethics; Chemistry; Science

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APA (6th Edition):

Danowitz, A. M. (2011). I. Synthesizing and Identifying Small Molecule Probes for Targeting Transcriptional Co-factors II. Design and Implementation of a Peer-Led Practical Research Ethics Module for Teaching Graduate Research Ethics. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/86294

Chicago Manual of Style (16th Edition):

Danowitz, Amy Marie. “I. Synthesizing and Identifying Small Molecule Probes for Targeting Transcriptional Co-factors II. Design and Implementation of a Peer-Led Practical Research Ethics Module for Teaching Graduate Research Ethics.” 2011. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/86294.

MLA Handbook (7th Edition):

Danowitz, Amy Marie. “I. Synthesizing and Identifying Small Molecule Probes for Targeting Transcriptional Co-factors II. Design and Implementation of a Peer-Led Practical Research Ethics Module for Teaching Graduate Research Ethics.” 2011. Web. 26 Jun 2019.

Vancouver:

Danowitz AM. I. Synthesizing and Identifying Small Molecule Probes for Targeting Transcriptional Co-factors II. Design and Implementation of a Peer-Led Practical Research Ethics Module for Teaching Graduate Research Ethics. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/86294.

Council of Science Editors:

Danowitz AM. I. Synthesizing and Identifying Small Molecule Probes for Targeting Transcriptional Co-factors II. Design and Implementation of a Peer-Led Practical Research Ethics Module for Teaching Graduate Research Ethics. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/86294


University of Michigan

4. Bates, Caleb A. Small Molecule Modulators of Transcription.

Degree: PhD, Medicinal Chemistry, 2010, University of Michigan

 Transcriptional activators are key components in the regulation of gene expression, being critical for precise, high fidelity transcription. Misregulation of transcription is a hallmark of… (more)

Subjects/Keywords: Gene Transcription; Chemistry; Science

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APA (6th Edition):

Bates, C. A. (2010). Small Molecule Modulators of Transcription. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/77704

Chicago Manual of Style (16th Edition):

Bates, Caleb A. “Small Molecule Modulators of Transcription.” 2010. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/77704.

MLA Handbook (7th Edition):

Bates, Caleb A. “Small Molecule Modulators of Transcription.” 2010. Web. 26 Jun 2019.

Vancouver:

Bates CA. Small Molecule Modulators of Transcription. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/77704.

Council of Science Editors:

Bates CA. Small Molecule Modulators of Transcription. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/77704


University of Michigan

5. Xu, Hao. Profiling Ester Prodrug Activation: An Activity Based Protein Profiling (ABPP) Approach.

Degree: PhD, Medicinal Chemistry, 2015, University of Michigan

 Determining the identity of prodrug activating enzyme(s) is key to understanding the mechanistic basis for enhanced cellular delivery, biodistribution, and prodrug stability. In addition, understanding… (more)

Subjects/Keywords: ABPP; Biological Chemistry; Science

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APA (6th Edition):

Xu, H. (2015). Profiling Ester Prodrug Activation: An Activity Based Protein Profiling (ABPP) Approach. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/113378

Chicago Manual of Style (16th Edition):

Xu, Hao. “Profiling Ester Prodrug Activation: An Activity Based Protein Profiling (ABPP) Approach.” 2015. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/113378.

MLA Handbook (7th Edition):

Xu, Hao. “Profiling Ester Prodrug Activation: An Activity Based Protein Profiling (ABPP) Approach.” 2015. Web. 26 Jun 2019.

Vancouver:

Xu H. Profiling Ester Prodrug Activation: An Activity Based Protein Profiling (ABPP) Approach. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/113378.

Council of Science Editors:

Xu H. Profiling Ester Prodrug Activation: An Activity Based Protein Profiling (ABPP) Approach. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/113378


University of Michigan

6. Emanuele, Anthony A. An Antibiotic Discovery Campaign Targeting VirF, the Main Transcriptional Regulator of Virulence in Shigella flexneri.

Degree: PhD, Medicinal Chemistry, 2016, University of Michigan

 Shigella flexneri is a gram-negative enteropathogen that infects the human colonic epithelium. It is estimated that Shigella spp. infect 165 million people a year worldwide.… (more)

Subjects/Keywords: Antibiotic Discovery Campaign; Shigella; Anti-virulence; VirF; Biological Chemistry; Microbiology and Immunology; Pharmacy and Pharmacology; Chemistry; Science (General); Health Sciences; Science

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APA (6th Edition):

Emanuele, A. A. (2016). An Antibiotic Discovery Campaign Targeting VirF, the Main Transcriptional Regulator of Virulence in Shigella flexneri. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120884

Chicago Manual of Style (16th Edition):

Emanuele, Anthony A. “An Antibiotic Discovery Campaign Targeting VirF, the Main Transcriptional Regulator of Virulence in Shigella flexneri.” 2016. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/120884.

MLA Handbook (7th Edition):

Emanuele, Anthony A. “An Antibiotic Discovery Campaign Targeting VirF, the Main Transcriptional Regulator of Virulence in Shigella flexneri.” 2016. Web. 26 Jun 2019.

Vancouver:

Emanuele AA. An Antibiotic Discovery Campaign Targeting VirF, the Main Transcriptional Regulator of Virulence in Shigella flexneri. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/120884.

Council of Science Editors:

Emanuele AA. An Antibiotic Discovery Campaign Targeting VirF, the Main Transcriptional Regulator of Virulence in Shigella flexneri. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120884


University of Michigan

7. Houghton, Jacob L. Towards Understanding and Overcoming the Antibiotic Resistance Conferred by Acetyltransferases.

Degree: PhD, Medicinal Chemistry, 2012, University of Michigan

 Aminoglycoside (AG) antibiotics have been widely applied to the treatment of bacterial infections since the discovery of streptomycin. Having enjoyed over 60 years of clinical… (more)

Subjects/Keywords: Antibacterial Resistance; Biological Chemistry; Chemistry; Science

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APA (6th Edition):

Houghton, J. L. (2012). Towards Understanding and Overcoming the Antibiotic Resistance Conferred by Acetyltransferases. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/96174

Chicago Manual of Style (16th Edition):

Houghton, Jacob L. “Towards Understanding and Overcoming the Antibiotic Resistance Conferred by Acetyltransferases.” 2012. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/96174.

MLA Handbook (7th Edition):

Houghton, Jacob L. “Towards Understanding and Overcoming the Antibiotic Resistance Conferred by Acetyltransferases.” 2012. Web. 26 Jun 2019.

Vancouver:

Houghton JL. Towards Understanding and Overcoming the Antibiotic Resistance Conferred by Acetyltransferases. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/96174.

Council of Science Editors:

Houghton JL. Towards Understanding and Overcoming the Antibiotic Resistance Conferred by Acetyltransferases. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/96174

8. Gibbons, Garrett S. The Histone Methyltransferase DOT1L: Discovery of Small-Molecule Inhibitors and its Role in Wnt Signaling.

Degree: PhD, Molecular and Cellular Pathology, 2014, University of Michigan

 Covalent post translational modifications of histone proteins are an important mechanism of epigenetic gene regulation that modulate chromatin structure. Methylation of histone lysine residues is… (more)

Subjects/Keywords: DOT1L; Epigenetics; Leukemia; Histone methyltransferase; Cancer; Chromatin; Biological Chemistry; Chemistry; Science

…trifluoromethansulfonate TRRAP - Transformation/transcription domain-associated protein UMD – University of… …Michigan Disruptor of H3K79 methylation UV-vis – ultra violet- visible light spectrum WDR5 – WD… 

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APA (6th Edition):

Gibbons, G. S. (2014). The Histone Methyltransferase DOT1L: Discovery of Small-Molecule Inhibitors and its Role in Wnt Signaling. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/110377

Chicago Manual of Style (16th Edition):

Gibbons, Garrett S. “The Histone Methyltransferase DOT1L: Discovery of Small-Molecule Inhibitors and its Role in Wnt Signaling.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/110377.

MLA Handbook (7th Edition):

Gibbons, Garrett S. “The Histone Methyltransferase DOT1L: Discovery of Small-Molecule Inhibitors and its Role in Wnt Signaling.” 2014. Web. 26 Jun 2019.

Vancouver:

Gibbons GS. The Histone Methyltransferase DOT1L: Discovery of Small-Molecule Inhibitors and its Role in Wnt Signaling. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/110377.

Council of Science Editors:

Gibbons GS. The Histone Methyltransferase DOT1L: Discovery of Small-Molecule Inhibitors and its Role in Wnt Signaling. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/110377

9. Makley, Leah Nicole. Chemical Approaches for ‘Undruggable’ Targets: The Discovery of Ligands for Small Heat Shock Proteins.

Degree: PhD, Medicinal Chemistry, 2014, University of Michigan

 Small heat shock proteins (sHSPs) are molecular chaperones that protect against protein aggregation in response to stress. These chaperones have been linked to a number… (more)

Subjects/Keywords: Drug Discovery; Medicinal Chemistry; Undruggable Targets; Small Heat Shock Proteins; Pharmacological Chaperones; Protein Misfolding; Chemistry; Science

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APA (6th Edition):

Makley, L. N. (2014). Chemical Approaches for ‘Undruggable’ Targets: The Discovery of Ligands for Small Heat Shock Proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/109032

Chicago Manual of Style (16th Edition):

Makley, Leah Nicole. “Chemical Approaches for ‘Undruggable’ Targets: The Discovery of Ligands for Small Heat Shock Proteins.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/109032.

MLA Handbook (7th Edition):

Makley, Leah Nicole. “Chemical Approaches for ‘Undruggable’ Targets: The Discovery of Ligands for Small Heat Shock Proteins.” 2014. Web. 26 Jun 2019.

Vancouver:

Makley LN. Chemical Approaches for ‘Undruggable’ Targets: The Discovery of Ligands for Small Heat Shock Proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/109032.

Council of Science Editors:

Makley LN. Chemical Approaches for ‘Undruggable’ Targets: The Discovery of Ligands for Small Heat Shock Proteins. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/109032

10. Hong, Jiyoung A. Toward the Discovery of Small Molecules that Target Adenosine 5'- Phosphosulfate Reductase.

Degree: PhD, Chemistry, 2012, University of Michigan

 Adenosine-5’-phosphosulfate reductase (APR) is an iron-sulfur protein that catalyzes the first committed step in the de novo biosynthesis of cysteine in mycobacteria. APR is a… (more)

Subjects/Keywords: Adenosine 5'-Phosphosulfate Reductase; Drug Design; Tuberculosis; Chemistry; Science

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APA (6th Edition):

Hong, J. A. (2012). Toward the Discovery of Small Molecules that Target Adenosine 5'- Phosphosulfate Reductase. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/91525

Chicago Manual of Style (16th Edition):

Hong, Jiyoung A. “Toward the Discovery of Small Molecules that Target Adenosine 5'- Phosphosulfate Reductase.” 2012. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/91525.

MLA Handbook (7th Edition):

Hong, Jiyoung A. “Toward the Discovery of Small Molecules that Target Adenosine 5'- Phosphosulfate Reductase.” 2012. Web. 26 Jun 2019.

Vancouver:

Hong JA. Toward the Discovery of Small Molecules that Target Adenosine 5'- Phosphosulfate Reductase. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/91525.

Council of Science Editors:

Hong JA. Toward the Discovery of Small Molecules that Target Adenosine 5'- Phosphosulfate Reductase. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/91525

11. Brooks, Allen F. Synthesis of Tritium Labeled Queuine, PreQ1 and Related Azide Probes Toward Examining the Prevalence of Queuine.

Degree: PhD, Medicinal Chemistry, 2012, University of Michigan

 Queuine is a modified nucleotide known to occur in the anticodon of four tRNAs. The queuine modification occurs across all eukaryotes and eubacteria with few… (more)

Subjects/Keywords: Queuine; PreQ1; Synthesis of Pyrrolopyrimidine; Chemistry; Science

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APA (6th Edition):

Brooks, A. F. (2012). Synthesis of Tritium Labeled Queuine, PreQ1 and Related Azide Probes Toward Examining the Prevalence of Queuine. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/91387

Chicago Manual of Style (16th Edition):

Brooks, Allen F. “Synthesis of Tritium Labeled Queuine, PreQ1 and Related Azide Probes Toward Examining the Prevalence of Queuine.” 2012. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/91387.

MLA Handbook (7th Edition):

Brooks, Allen F. “Synthesis of Tritium Labeled Queuine, PreQ1 and Related Azide Probes Toward Examining the Prevalence of Queuine.” 2012. Web. 26 Jun 2019.

Vancouver:

Brooks AF. Synthesis of Tritium Labeled Queuine, PreQ1 and Related Azide Probes Toward Examining the Prevalence of Queuine. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/91387.

Council of Science Editors:

Brooks AF. Synthesis of Tritium Labeled Queuine, PreQ1 and Related Azide Probes Toward Examining the Prevalence of Queuine. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/91387

12. Patrone, James D. Investigating Phosphopantothenoylcysteine Synthetase as a Potential Antibacterial Target.

Degree: PhD, Medicinal Chemistry, 2010, University of Michigan

 Phosphopantothenoylcysteine synthetase (PPCS) is the second enzyme in the universal Coenzyme A (CoA) biosynthetic pathway. PPCS is responsible for catalyzing the condensation of 4’-phosphopantothenate (PPA)… (more)

Subjects/Keywords: Pantothenate; Vitamin B5; Coenzyme A; PPCS; Pharmacy and Pharmacology; Health Sciences

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APA (6th Edition):

Patrone, J. D. (2010). Investigating Phosphopantothenoylcysteine Synthetase as a Potential Antibacterial Target. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/78970

Chicago Manual of Style (16th Edition):

Patrone, James D. “Investigating Phosphopantothenoylcysteine Synthetase as a Potential Antibacterial Target.” 2010. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/78970.

MLA Handbook (7th Edition):

Patrone, James D. “Investigating Phosphopantothenoylcysteine Synthetase as a Potential Antibacterial Target.” 2010. Web. 26 Jun 2019.

Vancouver:

Patrone JD. Investigating Phosphopantothenoylcysteine Synthetase as a Potential Antibacterial Target. [Internet] [Doctoral dissertation]. University of Michigan; 2010. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/78970.

Council of Science Editors:

Patrone JD. Investigating Phosphopantothenoylcysteine Synthetase as a Potential Antibacterial Target. [Doctoral Dissertation]. University of Michigan; 2010. Available from: http://hdl.handle.net/2027.42/78970

13. Atwal, Sumandeep Kaur. In vitro Characterization of Wild-type and Rifamycin-resistant Mycobacterium tuberculosis RNA polymerases.

Degree: PhD, Chemical Biology, 2012, University of Michigan

 Rifampin (a semi-synthetic rifamycin derivative) is one of the first-line anti-tuberculosis drugs. Rifampin inhibits transcription by binding to the beta-subunit of the RNA polymerase (RNAP).… (more)

Subjects/Keywords: Mycobacterium Tuberculosis; RNA Polymerase; Rifamycins; Biological Chemistry; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Atwal, S. K. (2012). In vitro Characterization of Wild-type and Rifamycin-resistant Mycobacterium tuberculosis RNA polymerases. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/94011

Chicago Manual of Style (16th Edition):

Atwal, Sumandeep Kaur. “In vitro Characterization of Wild-type and Rifamycin-resistant Mycobacterium tuberculosis RNA polymerases.” 2012. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/94011.

MLA Handbook (7th Edition):

Atwal, Sumandeep Kaur. “In vitro Characterization of Wild-type and Rifamycin-resistant Mycobacterium tuberculosis RNA polymerases.” 2012. Web. 26 Jun 2019.

Vancouver:

Atwal SK. In vitro Characterization of Wild-type and Rifamycin-resistant Mycobacterium tuberculosis RNA polymerases. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/94011.

Council of Science Editors:

Atwal SK. In vitro Characterization of Wild-type and Rifamycin-resistant Mycobacterium tuberculosis RNA polymerases. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/94011


University of Michigan

14. Turbiak, Anjanette J. The Synthesis and Exploration of Potential New Antagonists of the Wnt Signaling Pathway: New Leads to Treat Colon Cancer? Or, Not Quite?.

Degree: PhD, Medicinal Chemistry, 2009, University of Michigan

 Colorectal cancer continues to be a major health concern with over 150,000 new cases diagnosed each year in the United States alone. Nonetheless, the mutations… (more)

Subjects/Keywords: Wnt Signaling; Pyrimidotriazine; Pyrimidopyridazine; Pyrazolopyrimidine; Colon Cancer; Chemistry; Science

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APA (6th Edition):

Turbiak, A. J. (2009). The Synthesis and Exploration of Potential New Antagonists of the Wnt Signaling Pathway: New Leads to Treat Colon Cancer? Or, Not Quite?. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/64688

Chicago Manual of Style (16th Edition):

Turbiak, Anjanette J. “The Synthesis and Exploration of Potential New Antagonists of the Wnt Signaling Pathway: New Leads to Treat Colon Cancer? Or, Not Quite?.” 2009. Doctoral Dissertation, University of Michigan. Accessed June 26, 2019. http://hdl.handle.net/2027.42/64688.

MLA Handbook (7th Edition):

Turbiak, Anjanette J. “The Synthesis and Exploration of Potential New Antagonists of the Wnt Signaling Pathway: New Leads to Treat Colon Cancer? Or, Not Quite?.” 2009. Web. 26 Jun 2019.

Vancouver:

Turbiak AJ. The Synthesis and Exploration of Potential New Antagonists of the Wnt Signaling Pathway: New Leads to Treat Colon Cancer? Or, Not Quite?. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2027.42/64688.

Council of Science Editors:

Turbiak AJ. The Synthesis and Exploration of Potential New Antagonists of the Wnt Signaling Pathway: New Leads to Treat Colon Cancer? Or, Not Quite?. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/64688

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