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You searched for subject:(Medicinal Chemistry). Showing records 1 – 30 of 989 total matches.

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University of Minnesota

1. Ming, Xun. I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin.

Degree: 2011, University of Minnesota

University of Minnesota M.S. thesis. May 2011. Major: Medicinal Chemistry. Advisor:Dr. Natalia Y. Tretyakova. 1 computer file (PDF); xix, 200 pages.

1,1,2,2- Cis-diamminedichloroplatinum (II) (cisplatin)… (more)

Subjects/Keywords: Medicinal chemistry

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APA (6th Edition):

Ming, X. (2011). I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/109187

Chicago Manual of Style (16th Edition):

Ming, Xun. “I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin.” 2011. Masters Thesis, University of Minnesota. Accessed September 20, 2020. http://purl.umn.edu/109187.

MLA Handbook (7th Edition):

Ming, Xun. “I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin.” 2011. Web. 20 Sep 2020.

Vancouver:

Ming X. I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin. [Internet] [Masters thesis]. University of Minnesota; 2011. [cited 2020 Sep 20]. Available from: http://purl.umn.edu/109187.

Council of Science Editors:

Ming X. I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin. [Masters Thesis]. University of Minnesota; 2011. Available from: http://purl.umn.edu/109187


University of Minnesota

2. Pietsch, Kathryn Elizabeth. Chemical aspects of acylfulvene bioactivation to a cytotoxic reactive intermediate.

Degree: MS, Medicinal Chemistry, 2009, University of Minnesota

University of Minnesota M.S. thesis. December 2009. Major: Medicinal Chemistry. Advisor: Professor Shana J. Sturla, Ph.D. 1 computer file (PDF); iv, 34 pages.

Understanding molecular… (more)

Subjects/Keywords: Medicinal Chemistry

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APA (6th Edition):

Pietsch, K. E. (2009). Chemical aspects of acylfulvene bioactivation to a cytotoxic reactive intermediate. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/120273

Chicago Manual of Style (16th Edition):

Pietsch, Kathryn Elizabeth. “Chemical aspects of acylfulvene bioactivation to a cytotoxic reactive intermediate.” 2009. Masters Thesis, University of Minnesota. Accessed September 20, 2020. http://purl.umn.edu/120273.

MLA Handbook (7th Edition):

Pietsch, Kathryn Elizabeth. “Chemical aspects of acylfulvene bioactivation to a cytotoxic reactive intermediate.” 2009. Web. 20 Sep 2020.

Vancouver:

Pietsch KE. Chemical aspects of acylfulvene bioactivation to a cytotoxic reactive intermediate. [Internet] [Masters thesis]. University of Minnesota; 2009. [cited 2020 Sep 20]. Available from: http://purl.umn.edu/120273.

Council of Science Editors:

Pietsch KE. Chemical aspects of acylfulvene bioactivation to a cytotoxic reactive intermediate. [Masters Thesis]. University of Minnesota; 2009. Available from: http://purl.umn.edu/120273


University of Minnesota

3. Ming, Xun. I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin.

Degree: MS, Medicinal Chemistry, 2011, University of Minnesota

 1,1,2,2- Cis-diamminedichloroplatinum (II) (cisplatin) is a common anticancer drug used in treatment of solid tumors. The biological activity of cisplatin is generally attributed to its… (more)

Subjects/Keywords: Medicinal chemistry

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APA (6th Edition):

Ming, X. (2011). I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/109187

Chicago Manual of Style (16th Edition):

Ming, Xun. “I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin.” 2011. Masters Thesis, University of Minnesota. Accessed September 20, 2020. http://purl.umn.edu/109187.

MLA Handbook (7th Edition):

Ming, Xun. “I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin.” 2011. Web. 20 Sep 2020.

Vancouver:

Ming X. I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin. [Internet] [Masters thesis]. University of Minnesota; 2011. [cited 2020 Sep 20]. Available from: http://purl.umn.edu/109187.

Council of Science Editors:

Ming X. I. DNA-protein cross-linking by CIS-1,1,2,2-diamminedichloroplatinum (II) (cisplatin) II. formation of 8-OXO-dG and oxazolone lesions with p53 II. derived DNA sequences following photooxidation in the presence of riboflavin. [Masters Thesis]. University of Minnesota; 2011. Available from: http://purl.umn.edu/109187


University of Southern California

4. Gaffney, Kevin J. Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators.

Degree: PhD, Chemistry, 2015, University of Southern California

 This dissertation details my efforts towards the design and development of novel small molecules anti-cancer agents including joint efforts with a host of colleagues and… (more)

Subjects/Keywords: medicinal chemistry

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

APA (6th Edition):

Gaffney, K. J. (2015). Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556

Chicago Manual of Style (16th Edition):

Gaffney, Kevin J. “Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators.” 2015. Doctoral Dissertation, University of Southern California. Accessed September 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556.

MLA Handbook (7th Edition):

Gaffney, Kevin J. “Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators.” 2015. Web. 20 Sep 2020.

Vancouver:

Gaffney KJ. Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Sep 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556.

Council of Science Editors:

Gaffney KJ. Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556


Duquesne University

5. Velagaleti, Ranganadh. Dopamine Transporter (DAT) and Metabotropic Glutamate Receptor 5 (MGLU5) Irreversible Probes for Identifying Anti-Psychostimulant Therapeutics.

Degree: PhD, Medicinal Chemistry, 2014, Duquesne University

 Numerous behavioral studies indicate that dopamine transporter (DAT) inhibitors and metabotropic glutamate receptor 5 (mGlu5) negative allosteric modulators (NAMs) possess promising anti-addiction therapeutic properties. However,… (more)

Subjects/Keywords: Chemistry; Medicinal

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APA (6th Edition):

Velagaleti, R. (2014). Dopamine Transporter (DAT) and Metabotropic Glutamate Receptor 5 (MGLU5) Irreversible Probes for Identifying Anti-Psychostimulant Therapeutics. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1306

Chicago Manual of Style (16th Edition):

Velagaleti, Ranganadh. “Dopamine Transporter (DAT) and Metabotropic Glutamate Receptor 5 (MGLU5) Irreversible Probes for Identifying Anti-Psychostimulant Therapeutics.” 2014. Doctoral Dissertation, Duquesne University. Accessed September 20, 2020. https://dsc.duq.edu/etd/1306.

MLA Handbook (7th Edition):

Velagaleti, Ranganadh. “Dopamine Transporter (DAT) and Metabotropic Glutamate Receptor 5 (MGLU5) Irreversible Probes for Identifying Anti-Psychostimulant Therapeutics.” 2014. Web. 20 Sep 2020.

Vancouver:

Velagaleti R. Dopamine Transporter (DAT) and Metabotropic Glutamate Receptor 5 (MGLU5) Irreversible Probes for Identifying Anti-Psychostimulant Therapeutics. [Internet] [Doctoral dissertation]. Duquesne University; 2014. [cited 2020 Sep 20]. Available from: https://dsc.duq.edu/etd/1306.

Council of Science Editors:

Velagaleti R. Dopamine Transporter (DAT) and Metabotropic Glutamate Receptor 5 (MGLU5) Irreversible Probes for Identifying Anti-Psychostimulant Therapeutics. [Doctoral Dissertation]. Duquesne University; 2014. Available from: https://dsc.duq.edu/etd/1306


University of Montana

6. Steiger, Scott. The Synthesis and study of heterocyclic, dimeric and chiral ligands for the multidrug-resistance transporter.

Degree: PhD, 2014, University of Montana

 The development of multidrug resistance in tumor cells has been recognized as a major obstacle to successful cancer treatment. Tumor cells in vitro and in… (more)

Subjects/Keywords: Medicinal Chemistry

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APA (6th Edition):

Steiger, S. (2014). The Synthesis and study of heterocyclic, dimeric and chiral ligands for the multidrug-resistance transporter. (Doctoral Dissertation). University of Montana. Retrieved from https://scholarworks.umt.edu/etd/4406

Chicago Manual of Style (16th Edition):

Steiger, Scott. “The Synthesis and study of heterocyclic, dimeric and chiral ligands for the multidrug-resistance transporter.” 2014. Doctoral Dissertation, University of Montana. Accessed September 20, 2020. https://scholarworks.umt.edu/etd/4406.

MLA Handbook (7th Edition):

Steiger, Scott. “The Synthesis and study of heterocyclic, dimeric and chiral ligands for the multidrug-resistance transporter.” 2014. Web. 20 Sep 2020.

Vancouver:

Steiger S. The Synthesis and study of heterocyclic, dimeric and chiral ligands for the multidrug-resistance transporter. [Internet] [Doctoral dissertation]. University of Montana; 2014. [cited 2020 Sep 20]. Available from: https://scholarworks.umt.edu/etd/4406.

Council of Science Editors:

Steiger S. The Synthesis and study of heterocyclic, dimeric and chiral ligands for the multidrug-resistance transporter. [Doctoral Dissertation]. University of Montana; 2014. Available from: https://scholarworks.umt.edu/etd/4406


University of Lund

7. Fritz, Helena. Axl RTK and microRNAs in urogenital cancers.

Degree: 2015, University of Lund

 This thesis is based on four projects focused on the Axl receptor tyrosine kinase (RTK) and microRNAs in clear cell renal cell carcinoma (ccRCC) and… (more)

Subjects/Keywords: Medicinal Chemistry

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APA (6th Edition):

Fritz, H. (2015). Axl RTK and microRNAs in urogenital cancers. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/5366241 ; https://portal.research.lu.se/ws/files/3435302/5366247.pdf

Chicago Manual of Style (16th Edition):

Fritz, Helena. “Axl RTK and microRNAs in urogenital cancers.” 2015. Doctoral Dissertation, University of Lund. Accessed September 20, 2020. https://lup.lub.lu.se/record/5366241 ; https://portal.research.lu.se/ws/files/3435302/5366247.pdf.

MLA Handbook (7th Edition):

Fritz, Helena. “Axl RTK and microRNAs in urogenital cancers.” 2015. Web. 20 Sep 2020.

Vancouver:

Fritz H. Axl RTK and microRNAs in urogenital cancers. [Internet] [Doctoral dissertation]. University of Lund; 2015. [cited 2020 Sep 20]. Available from: https://lup.lub.lu.se/record/5366241 ; https://portal.research.lu.se/ws/files/3435302/5366247.pdf.

Council of Science Editors:

Fritz H. Axl RTK and microRNAs in urogenital cancers. [Doctoral Dissertation]. University of Lund; 2015. Available from: https://lup.lub.lu.se/record/5366241 ; https://portal.research.lu.se/ws/files/3435302/5366247.pdf

8. Njaria, Paul Magutu. Antimycobacterial 2-aminoquinazolinones and benzoxazole-based oximes: synthesis, biological evaluation, physicochemical profiling and supramolecular derivatization.

Degree: Image, Chemistry, 2017, University of Cape Town

 Tuberculosis (TB) is a life-threatening infectious disease caused by Mycobacterium tuberculosis (Mtb). Globally, TB is a major public health burden with an estimated 10.4 million… (more)

Subjects/Keywords: Chemistry; Medicinal Chemistry

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APA (6th Edition):

Njaria, P. M. (2017). Antimycobacterial 2-aminoquinazolinones and benzoxazole-based oximes: synthesis, biological evaluation, physicochemical profiling and supramolecular derivatization. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/26954

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

Chicago Manual of Style (16th Edition):

Njaria, Paul Magutu. “Antimycobacterial 2-aminoquinazolinones and benzoxazole-based oximes: synthesis, biological evaluation, physicochemical profiling and supramolecular derivatization.” 2017. Thesis, University of Cape Town. Accessed September 20, 2020. http://hdl.handle.net/11427/26954.

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

MLA Handbook (7th Edition):

Njaria, Paul Magutu. “Antimycobacterial 2-aminoquinazolinones and benzoxazole-based oximes: synthesis, biological evaluation, physicochemical profiling and supramolecular derivatization.” 2017. Web. 20 Sep 2020.

Vancouver:

Njaria PM. Antimycobacterial 2-aminoquinazolinones and benzoxazole-based oximes: synthesis, biological evaluation, physicochemical profiling and supramolecular derivatization. [Internet] [Thesis]. University of Cape Town; 2017. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/11427/26954.

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

Council of Science Editors:

Njaria PM. Antimycobacterial 2-aminoquinazolinones and benzoxazole-based oximes: synthesis, biological evaluation, physicochemical profiling and supramolecular derivatization. [Thesis]. University of Cape Town; 2017. Available from: http://hdl.handle.net/11427/26954

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


University of Oxford

9. Wilkinson, Isabel. Mechanism of action studies of the utrophin modulator ezutromid for the treatment of Duchenne muscular dystrophy.

Degree: PhD, 2019, University of Oxford

 Duchenne muscular dystrophy (DMD) is a muscle wasting disease arising from mutations in the dystrophin gene, affecting about 1 in 5000 boys. Whilst there is… (more)

Subjects/Keywords: Organic Chemistry; Medicinal Chemistry; Chemistry

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APA (6th Edition):

Wilkinson, I. (2019). Mechanism of action studies of the utrophin modulator ezutromid for the treatment of Duchenne muscular dystrophy. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:47554767-9235-4319-8911-5eb827081044 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799935

Chicago Manual of Style (16th Edition):

Wilkinson, Isabel. “Mechanism of action studies of the utrophin modulator ezutromid for the treatment of Duchenne muscular dystrophy.” 2019. Doctoral Dissertation, University of Oxford. Accessed September 20, 2020. http://ora.ox.ac.uk/objects/uuid:47554767-9235-4319-8911-5eb827081044 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799935.

MLA Handbook (7th Edition):

Wilkinson, Isabel. “Mechanism of action studies of the utrophin modulator ezutromid for the treatment of Duchenne muscular dystrophy.” 2019. Web. 20 Sep 2020.

Vancouver:

Wilkinson I. Mechanism of action studies of the utrophin modulator ezutromid for the treatment of Duchenne muscular dystrophy. [Internet] [Doctoral dissertation]. University of Oxford; 2019. [cited 2020 Sep 20]. Available from: http://ora.ox.ac.uk/objects/uuid:47554767-9235-4319-8911-5eb827081044 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799935.

Council of Science Editors:

Wilkinson I. Mechanism of action studies of the utrophin modulator ezutromid for the treatment of Duchenne muscular dystrophy. [Doctoral Dissertation]. University of Oxford; 2019. Available from: http://ora.ox.ac.uk/objects/uuid:47554767-9235-4319-8911-5eb827081044 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799935


University of Notre Dame

10. Andrew Ward. Improved Synthesis of the Novel Anti-Tuberculosis Drug SQ109 and Synthesis of Nitroso-ene Analogs</h1>.

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

  Despite the advances made in the middle of the 20th century to combat tuberculosis, the current short-course therapy has been met with challenges from… (more)

Subjects/Keywords: tuberculosis; medicinal chemistry

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APA (6th Edition):

Ward, A. (2011). Improved Synthesis of the Novel Anti-Tuberculosis Drug SQ109 and Synthesis of Nitroso-ene Analogs</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/n296ww74p23

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

Chicago Manual of Style (16th Edition):

Ward, Andrew. “Improved Synthesis of the Novel Anti-Tuberculosis Drug SQ109 and Synthesis of Nitroso-ene Analogs</h1>.” 2011. Thesis, University of Notre Dame. Accessed September 20, 2020. https://curate.nd.edu/show/n296ww74p23.

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

MLA Handbook (7th Edition):

Ward, Andrew. “Improved Synthesis of the Novel Anti-Tuberculosis Drug SQ109 and Synthesis of Nitroso-ene Analogs</h1>.” 2011. Web. 20 Sep 2020.

Vancouver:

Ward A. Improved Synthesis of the Novel Anti-Tuberculosis Drug SQ109 and Synthesis of Nitroso-ene Analogs</h1>. [Internet] [Thesis]. University of Notre Dame; 2011. [cited 2020 Sep 20]. Available from: https://curate.nd.edu/show/n296ww74p23.

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

Council of Science Editors:

Ward A. Improved Synthesis of the Novel Anti-Tuberculosis Drug SQ109 and Synthesis of Nitroso-ene Analogs</h1>. [Thesis]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/n296ww74p23

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


Duquesne University

11. Choudhary, Shruti. Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection.

Degree: PhD, Medicinal Chemistry, 2017, Duquesne University

  Dose limiting toxicity and development of multidrug resistance by the tumors are the major limitations of current cancer chemotherapy. Microtubule targeting agents (MTAs) are… (more)

Subjects/Keywords: Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Choudhary, S. (2017). Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/233

Chicago Manual of Style (16th Edition):

Choudhary, Shruti. “Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection.” 2017. Doctoral Dissertation, Duquesne University. Accessed September 20, 2020. https://dsc.duq.edu/etd/233.

MLA Handbook (7th Edition):

Choudhary, Shruti. “Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection.” 2017. Web. 20 Sep 2020.

Vancouver:

Choudhary S. Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection. [Internet] [Doctoral dissertation]. Duquesne University; 2017. [cited 2020 Sep 20]. Available from: https://dsc.duq.edu/etd/233.

Council of Science Editors:

Choudhary S. Target Based Design And Synthesis of Heterocycles in the Potential Treatment of Cancer and Opportunistic Infection. [Doctoral Dissertation]. Duquesne University; 2017. Available from: https://dsc.duq.edu/etd/233


UCLA

12. Hollibaugh, Ryan. Defining a Minimal Pharmacophore to Selectively Inhibit MBOAT4 (Ghrelin O-Acyl Transferase).

Degree: Chemistry, 2016, UCLA

 Ghrelin O-acyl Transferase (GOAT) is a recently discovered member of the membrane bound O-acyl transferase (MBOAT) family of enzymes. GOAT is uniquely able to catalyze… (more)

Subjects/Keywords: Organic chemistry; Ghrelin; Medicinal Chemistry

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APA (6th Edition):

Hollibaugh, R. (2016). Defining a Minimal Pharmacophore to Selectively Inhibit MBOAT4 (Ghrelin O-Acyl Transferase). (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/0971212d

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

Chicago Manual of Style (16th Edition):

Hollibaugh, Ryan. “Defining a Minimal Pharmacophore to Selectively Inhibit MBOAT4 (Ghrelin O-Acyl Transferase).” 2016. Thesis, UCLA. Accessed September 20, 2020. http://www.escholarship.org/uc/item/0971212d.

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

MLA Handbook (7th Edition):

Hollibaugh, Ryan. “Defining a Minimal Pharmacophore to Selectively Inhibit MBOAT4 (Ghrelin O-Acyl Transferase).” 2016. Web. 20 Sep 2020.

Vancouver:

Hollibaugh R. Defining a Minimal Pharmacophore to Selectively Inhibit MBOAT4 (Ghrelin O-Acyl Transferase). [Internet] [Thesis]. UCLA; 2016. [cited 2020 Sep 20]. Available from: http://www.escholarship.org/uc/item/0971212d.

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

Council of Science Editors:

Hollibaugh R. Defining a Minimal Pharmacophore to Selectively Inhibit MBOAT4 (Ghrelin O-Acyl Transferase). [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/0971212d

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

13. Arjaibi, Hajer. Investigation onto the Mechanism Behind the Hepatoprotective Effect of Cucurbitacin Compounds.

Degree: MS, Chemistry and Biochemistry, 2013, South Dakota State University

  Hepatocellular Carcinoma (HCC) is the fourth leading cause of death worldwide. HCC is one major example of inflammatory-associated cancer. Aggressive resection or liver transplantation… (more)

Subjects/Keywords: Chemistry; Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Arjaibi, H. (2013). Investigation onto the Mechanism Behind the Hepatoprotective Effect of Cucurbitacin Compounds. (Masters Thesis). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1374

Chicago Manual of Style (16th Edition):

Arjaibi, Hajer. “Investigation onto the Mechanism Behind the Hepatoprotective Effect of Cucurbitacin Compounds.” 2013. Masters Thesis, South Dakota State University. Accessed September 20, 2020. http://openprairie.sdstate.edu/etd/1374.

MLA Handbook (7th Edition):

Arjaibi, Hajer. “Investigation onto the Mechanism Behind the Hepatoprotective Effect of Cucurbitacin Compounds.” 2013. Web. 20 Sep 2020.

Vancouver:

Arjaibi H. Investigation onto the Mechanism Behind the Hepatoprotective Effect of Cucurbitacin Compounds. [Internet] [Masters thesis]. South Dakota State University; 2013. [cited 2020 Sep 20]. Available from: http://openprairie.sdstate.edu/etd/1374.

Council of Science Editors:

Arjaibi H. Investigation onto the Mechanism Behind the Hepatoprotective Effect of Cucurbitacin Compounds. [Masters Thesis]. South Dakota State University; 2013. Available from: http://openprairie.sdstate.edu/etd/1374


University of Michigan

14. Madak, Joseph. Design and Synthesis of Novel Dihydroorotate Dehydrogenase Inhibitors.

Degree: PhD, Medicinal Chemistry, 2018, University of Michigan

 Rapidly growing cells are dependent on sufficient concentrations of nucleotides to sustain proliferation. One enzyme essential for the de novo synthesis of pyrimidine-based nucleotides is… (more)

Subjects/Keywords: Medicinal Chemistry; Biological Chemistry; Science

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APA (6th Edition):

Madak, J. (2018). Design and Synthesis of Novel Dihydroorotate Dehydrogenase Inhibitors. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/144184

Chicago Manual of Style (16th Edition):

Madak, Joseph. “Design and Synthesis of Novel Dihydroorotate Dehydrogenase Inhibitors.” 2018. Doctoral Dissertation, University of Michigan. Accessed September 20, 2020. http://hdl.handle.net/2027.42/144184.

MLA Handbook (7th Edition):

Madak, Joseph. “Design and Synthesis of Novel Dihydroorotate Dehydrogenase Inhibitors.” 2018. Web. 20 Sep 2020.

Vancouver:

Madak J. Design and Synthesis of Novel Dihydroorotate Dehydrogenase Inhibitors. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2027.42/144184.

Council of Science Editors:

Madak J. Design and Synthesis of Novel Dihydroorotate Dehydrogenase Inhibitors. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/144184


University of Oklahoma

15. Dou, Xiaozheng. HARNESSING SMALL-MOLECULE PROTEIN STIMULATION TO DEVELOP NEW LEADS FOR RETINAL AND INFECTIOUS DISEASES.

Degree: PhD, 2020, University of Oklahoma

 This dissertation describes the development of new therapeutic leads for retinal (chapter 1-3) and infectious diseases (chapter 4). More than 40% of patients with retinal… (more)

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

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APA (6th Edition):

Dou, X. (2020). HARNESSING SMALL-MOLECULE PROTEIN STIMULATION TO DEVELOP NEW LEADS FOR RETINAL AND INFECTIOUS DISEASES. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/325205

Chicago Manual of Style (16th Edition):

Dou, Xiaozheng. “HARNESSING SMALL-MOLECULE PROTEIN STIMULATION TO DEVELOP NEW LEADS FOR RETINAL AND INFECTIOUS DISEASES.” 2020. Doctoral Dissertation, University of Oklahoma. Accessed September 20, 2020. http://hdl.handle.net/11244/325205.

MLA Handbook (7th Edition):

Dou, Xiaozheng. “HARNESSING SMALL-MOLECULE PROTEIN STIMULATION TO DEVELOP NEW LEADS FOR RETINAL AND INFECTIOUS DISEASES.” 2020. Web. 20 Sep 2020.

Vancouver:

Dou X. HARNESSING SMALL-MOLECULE PROTEIN STIMULATION TO DEVELOP NEW LEADS FOR RETINAL AND INFECTIOUS DISEASES. [Internet] [Doctoral dissertation]. University of Oklahoma; 2020. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/11244/325205.

Council of Science Editors:

Dou X. HARNESSING SMALL-MOLECULE PROTEIN STIMULATION TO DEVELOP NEW LEADS FOR RETINAL AND INFECTIOUS DISEASES. [Doctoral Dissertation]. University of Oklahoma; 2020. Available from: http://hdl.handle.net/11244/325205

16. Alshehri, Saad Ali. Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia.

Degree: PhD, Chemistry and Biochemistry, 2020, South Dakota State University

  Diabetes mellitus (DM) is a metabolic disease characterized by high levels of blood glucose resulting from defects in insulin production or action. A world-wide… (more)

Subjects/Keywords: Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Alshehri, S. A. (2020). Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia. (Doctoral Dissertation). South Dakota State University. Retrieved from https://openprairie.sdstate.edu/etd/4101

Chicago Manual of Style (16th Edition):

Alshehri, Saad Ali. “Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia.” 2020. Doctoral Dissertation, South Dakota State University. Accessed September 20, 2020. https://openprairie.sdstate.edu/etd/4101.

MLA Handbook (7th Edition):

Alshehri, Saad Ali. “Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia.” 2020. Web. 20 Sep 2020.

Vancouver:

Alshehri SA. Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia. [Internet] [Doctoral dissertation]. South Dakota State University; 2020. [cited 2020 Sep 20]. Available from: https://openprairie.sdstate.edu/etd/4101.

Council of Science Editors:

Alshehri SA. Antidiabetic Activity of Cissus rotundifolia Plant Growing in Saudi Arabia. [Doctoral Dissertation]. South Dakota State University; 2020. Available from: https://openprairie.sdstate.edu/etd/4101


Northeastern University

17. Johnston, Meghan Ryan. Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands.

Degree: PhD, Department of Chemistry and Chemical Biology, 2012, Northeastern University

 The endocannabinoid system includes signaling ligands for the cannabinoid receptors, (CB1, CB2) as well as the enzymes that that are responsible for their biosynthesis and… (more)

Subjects/Keywords: Chemistry; Medicinal-Pharmaceutical Chemistry

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APA (6th Edition):

Johnston, M. R. (2012). Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002760

Chicago Manual of Style (16th Edition):

Johnston, Meghan Ryan. “Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands.” 2012. Doctoral Dissertation, Northeastern University. Accessed September 20, 2020. http://hdl.handle.net/2047/d20002760.

MLA Handbook (7th Edition):

Johnston, Meghan Ryan. “Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands.” 2012. Web. 20 Sep 2020.

Vancouver:

Johnston MR. Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/2047/d20002760.

Council of Science Editors:

Johnston MR. Endocannabinoid enzymes monoacylglycerol lipase and diacylglycerol lipase: biochemical studies and novel ligands. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002760

18. Mishra, Sanket J. Structure-Based Design of Grp94-Selective Inhibitors.

Degree: MS, Medicinal Chemistry, 2014, University of Kansas

 Heat shock protein 90 KDa (Hsp90) belongs to family of proteins called molecular chaperone that are associated with protein folding and maturation. Hsp90 clients play… (more)

Subjects/Keywords: Pharmaceutical sciences; Chemistry; Medicinal Chemistry

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APA (6th Edition):

Mishra, S. J. (2014). Structure-Based Design of Grp94-Selective Inhibitors. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21649

Chicago Manual of Style (16th Edition):

Mishra, Sanket J. “Structure-Based Design of Grp94-Selective Inhibitors.” 2014. Masters Thesis, University of Kansas. Accessed September 20, 2020. http://hdl.handle.net/1808/21649.

MLA Handbook (7th Edition):

Mishra, Sanket J. “Structure-Based Design of Grp94-Selective Inhibitors.” 2014. Web. 20 Sep 2020.

Vancouver:

Mishra SJ. Structure-Based Design of Grp94-Selective Inhibitors. [Internet] [Masters thesis]. University of Kansas; 2014. [cited 2020 Sep 20]. Available from: http://hdl.handle.net/1808/21649.

Council of Science Editors:

Mishra SJ. Structure-Based Design of Grp94-Selective Inhibitors. [Masters Thesis]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/21649


Wayne State University

19. Li, Jing. Multifunctional bioreducible nanoparticles for gene therapy.

Degree: PhD, Pharmaceutical Sciences, 2012, Wayne State University

  Gene therapy is a promising therapeutic strategy to treat diseases caused by single or multiple gene mutations. Non-viral gene delivery vectors exhibit many advantages… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Li, J. (2012). Multifunctional bioreducible nanoparticles for gene therapy. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/573

Chicago Manual of Style (16th Edition):

Li, Jing. “Multifunctional bioreducible nanoparticles for gene therapy.” 2012. Doctoral Dissertation, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_dissertations/573.

MLA Handbook (7th Edition):

Li, Jing. “Multifunctional bioreducible nanoparticles for gene therapy.” 2012. Web. 20 Sep 2020.

Vancouver:

Li J. Multifunctional bioreducible nanoparticles for gene therapy. [Internet] [Doctoral dissertation]. Wayne State University; 2012. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/573.

Council of Science Editors:

Li J. Multifunctional bioreducible nanoparticles for gene therapy. [Doctoral Dissertation]. Wayne State University; 2012. Available from: https://digitalcommons.wayne.edu/oa_dissertations/573


Wayne State University

20. Modi, Gyan Prakash. Design, Synthesis, Biological Evaluation And Molecular Modeling Studies Of Novel Multifunctional Neuroprotective Drugs For The Treatment Of Parkinson's Disease: An Effort Towards The Improvement Of In Vivo Efficacy And Modulation Of Alpha Synuclein Aggregation Property Of The Neuroprotective Parent.

Degree: PhD, Pharmaceutical Sciences, 2013, Wayne State University

  DESIGN, SYNTHESIS, BIOLOGICAL EVALUATION AND MOLECULAR MODELING STUDIES OF NOVEL MULTIFUNCTIONAL NEUROPROTECTIVE DRUGS FOR THE TREATMENT OF PARKINSON'S DISEASE: AN EFFORT TOWARDS THE IMPROVEMENT… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Modi, G. P. (2013). Design, Synthesis, Biological Evaluation And Molecular Modeling Studies Of Novel Multifunctional Neuroprotective Drugs For The Treatment Of Parkinson's Disease: An Effort Towards The Improvement Of In Vivo Efficacy And Modulation Of Alpha Synuclein Aggregation Property Of The Neuroprotective Parent. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/905

Chicago Manual of Style (16th Edition):

Modi, Gyan Prakash. “Design, Synthesis, Biological Evaluation And Molecular Modeling Studies Of Novel Multifunctional Neuroprotective Drugs For The Treatment Of Parkinson's Disease: An Effort Towards The Improvement Of In Vivo Efficacy And Modulation Of Alpha Synuclein Aggregation Property Of The Neuroprotective Parent.” 2013. Doctoral Dissertation, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_dissertations/905.

MLA Handbook (7th Edition):

Modi, Gyan Prakash. “Design, Synthesis, Biological Evaluation And Molecular Modeling Studies Of Novel Multifunctional Neuroprotective Drugs For The Treatment Of Parkinson's Disease: An Effort Towards The Improvement Of In Vivo Efficacy And Modulation Of Alpha Synuclein Aggregation Property Of The Neuroprotective Parent.” 2013. Web. 20 Sep 2020.

Vancouver:

Modi GP. Design, Synthesis, Biological Evaluation And Molecular Modeling Studies Of Novel Multifunctional Neuroprotective Drugs For The Treatment Of Parkinson's Disease: An Effort Towards The Improvement Of In Vivo Efficacy And Modulation Of Alpha Synuclein Aggregation Property Of The Neuroprotective Parent. [Internet] [Doctoral dissertation]. Wayne State University; 2013. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/905.

Council of Science Editors:

Modi GP. Design, Synthesis, Biological Evaluation And Molecular Modeling Studies Of Novel Multifunctional Neuroprotective Drugs For The Treatment Of Parkinson's Disease: An Effort Towards The Improvement Of In Vivo Efficacy And Modulation Of Alpha Synuclein Aggregation Property Of The Neuroprotective Parent. [Doctoral Dissertation]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_dissertations/905


Wayne State University

21. Mohammed, Abiy Mussa. Mechanisms Of Cytokine-Induced Metabolic Dysfunction Of The Pancreatic Beta-Cell.

Degree: PhD, Pharmaceutical Sciences, 2013, Wayne State University

  MECHANISMS OF CYTOKINE-INDUCED METABOLIC DYSFUNCTION OF THE PANCREATIC BETA-CELL by ABIY MUSSA MOHAMMED August 2013 Advisor: Dr. Anjaneyulu Kowluru Major: Pharmaceutical Sciences Degree: Doctor… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Mohammed, A. M. (2013). Mechanisms Of Cytokine-Induced Metabolic Dysfunction Of The Pancreatic Beta-Cell. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/786

Chicago Manual of Style (16th Edition):

Mohammed, Abiy Mussa. “Mechanisms Of Cytokine-Induced Metabolic Dysfunction Of The Pancreatic Beta-Cell.” 2013. Doctoral Dissertation, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_dissertations/786.

MLA Handbook (7th Edition):

Mohammed, Abiy Mussa. “Mechanisms Of Cytokine-Induced Metabolic Dysfunction Of The Pancreatic Beta-Cell.” 2013. Web. 20 Sep 2020.

Vancouver:

Mohammed AM. Mechanisms Of Cytokine-Induced Metabolic Dysfunction Of The Pancreatic Beta-Cell. [Internet] [Doctoral dissertation]. Wayne State University; 2013. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/786.

Council of Science Editors:

Mohammed AM. Mechanisms Of Cytokine-Induced Metabolic Dysfunction Of The Pancreatic Beta-Cell. [Doctoral Dissertation]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_dissertations/786


Wayne State University

22. Johnson, Mark Andrew. Progress Towards Development Of Multifunctional, Dopamine D2/d3 Receptor Agonists As Symptomatic And Disease-Modifying Therapeutic Agents For Parkinson's Disease.

Degree: PhD, Pharmaceutical Sciences, 2013, Wayne State University

  Parkinson¡¯s disease (PD) is a progressive, neurodegenerative disorder that arises primarily through the loss of dopaminergic neurons in the substantia nigra pars compacta (SNc),… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Johnson, M. A. (2013). Progress Towards Development Of Multifunctional, Dopamine D2/d3 Receptor Agonists As Symptomatic And Disease-Modifying Therapeutic Agents For Parkinson's Disease. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/729

Chicago Manual of Style (16th Edition):

Johnson, Mark Andrew. “Progress Towards Development Of Multifunctional, Dopamine D2/d3 Receptor Agonists As Symptomatic And Disease-Modifying Therapeutic Agents For Parkinson's Disease.” 2013. Doctoral Dissertation, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_dissertations/729.

MLA Handbook (7th Edition):

Johnson, Mark Andrew. “Progress Towards Development Of Multifunctional, Dopamine D2/d3 Receptor Agonists As Symptomatic And Disease-Modifying Therapeutic Agents For Parkinson's Disease.” 2013. Web. 20 Sep 2020.

Vancouver:

Johnson MA. Progress Towards Development Of Multifunctional, Dopamine D2/d3 Receptor Agonists As Symptomatic And Disease-Modifying Therapeutic Agents For Parkinson's Disease. [Internet] [Doctoral dissertation]. Wayne State University; 2013. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/729.

Council of Science Editors:

Johnson MA. Progress Towards Development Of Multifunctional, Dopamine D2/d3 Receptor Agonists As Symptomatic And Disease-Modifying Therapeutic Agents For Parkinson's Disease. [Doctoral Dissertation]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_dissertations/729


Wayne State University

23. Khadija, Syeda. Islet Dysfunction In Diabetes.

Degree: PhD, Pharmaceutical Sciences, 2015, Wayne State University

  Type 2 Diabetes [T2DM] is a chronic condition resulting from gradual failure of pancreatic beta cells to synthesize and secrete sufficient insulin to meet… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Khadija, S. (2015). Islet Dysfunction In Diabetes. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1342

Chicago Manual of Style (16th Edition):

Khadija, Syeda. “Islet Dysfunction In Diabetes.” 2015. Doctoral Dissertation, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_dissertations/1342.

MLA Handbook (7th Edition):

Khadija, Syeda. “Islet Dysfunction In Diabetes.” 2015. Web. 20 Sep 2020.

Vancouver:

Khadija S. Islet Dysfunction In Diabetes. [Internet] [Doctoral dissertation]. Wayne State University; 2015. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1342.

Council of Science Editors:

Khadija S. Islet Dysfunction In Diabetes. [Doctoral Dissertation]. Wayne State University; 2015. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1342


Wayne State University

24. Killinger, Bryan Andrew. Axonal Transport, Parkin, And Α-Synuclein; Novel Therapeutic Targets To Treat Methamphetamine Neurotoxicity.

Degree: PhD, Pharmaceutical Sciences, 2017, Wayne State University

  Methamphetamine (METH) is a commonly abuse psychostimulant. Exposure to chronic high doses of METH can result in neurotoxicity primarily characterized by damage to striatal… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Killinger, B. A. (2017). Axonal Transport, Parkin, And Α-Synuclein; Novel Therapeutic Targets To Treat Methamphetamine Neurotoxicity. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1823

Chicago Manual of Style (16th Edition):

Killinger, Bryan Andrew. “Axonal Transport, Parkin, And Α-Synuclein; Novel Therapeutic Targets To Treat Methamphetamine Neurotoxicity.” 2017. Doctoral Dissertation, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_dissertations/1823.

MLA Handbook (7th Edition):

Killinger, Bryan Andrew. “Axonal Transport, Parkin, And Α-Synuclein; Novel Therapeutic Targets To Treat Methamphetamine Neurotoxicity.” 2017. Web. 20 Sep 2020.

Vancouver:

Killinger BA. Axonal Transport, Parkin, And Α-Synuclein; Novel Therapeutic Targets To Treat Methamphetamine Neurotoxicity. [Internet] [Doctoral dissertation]. Wayne State University; 2017. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1823.

Council of Science Editors:

Killinger BA. Axonal Transport, Parkin, And Α-Synuclein; Novel Therapeutic Targets To Treat Methamphetamine Neurotoxicity. [Doctoral Dissertation]. Wayne State University; 2017. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1823


Wayne State University

25. Li, Lingzhi. Underlying Mechanisms Of Arsenic-Induced Tumorigenesis: From Epigenetics To Malignancy.

Degree: PhD, Pharmaceutical Sciences, 2017, Wayne State University

  Arsenic is a well-recognized environmental health threat with the capability of inducing a number of human diseases, including cancer. The aim of this dissertation… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Li, L. (2017). Underlying Mechanisms Of Arsenic-Induced Tumorigenesis: From Epigenetics To Malignancy. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1834

Chicago Manual of Style (16th Edition):

Li, Lingzhi. “Underlying Mechanisms Of Arsenic-Induced Tumorigenesis: From Epigenetics To Malignancy.” 2017. Doctoral Dissertation, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_dissertations/1834.

MLA Handbook (7th Edition):

Li, Lingzhi. “Underlying Mechanisms Of Arsenic-Induced Tumorigenesis: From Epigenetics To Malignancy.” 2017. Web. 20 Sep 2020.

Vancouver:

Li L. Underlying Mechanisms Of Arsenic-Induced Tumorigenesis: From Epigenetics To Malignancy. [Internet] [Doctoral dissertation]. Wayne State University; 2017. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1834.

Council of Science Editors:

Li L. Underlying Mechanisms Of Arsenic-Induced Tumorigenesis: From Epigenetics To Malignancy. [Doctoral Dissertation]. Wayne State University; 2017. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1834


Virginia Commonwealth University

26. Raborg, Thomas. Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer.

Degree: MS, Pharmaceutical Sciences, 2014, Virginia Commonwealth University

  Chemokine receptor CCR5 (CCR5) is a G-protein coupled receptor (GPCR) predominantly expressed on leukocytes, or white blood cells.1–3 During inflammation, the body releases chemokines… (more)

Subjects/Keywords: Medicinal and Pharmaceutical Chemistry

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APA (6th Edition):

Raborg, T. (2014). Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553

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

Chicago Manual of Style (16th Edition):

Raborg, Thomas. “Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer.” 2014. Thesis, Virginia Commonwealth University. Accessed September 20, 2020. https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553.

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

MLA Handbook (7th Edition):

Raborg, Thomas. “Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer.” 2014. Web. 20 Sep 2020.

Vancouver:

Raborg T. Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer. [Internet] [Thesis]. Virginia Commonwealth University; 2014. [cited 2020 Sep 20]. Available from: https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553.

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

Council of Science Editors:

Raborg T. Development of Bivalent Ligands Targeting the Putative CCR5-MOR Heterodimer. [Thesis]. Virginia Commonwealth University; 2014. Available from: https://doi.org/10.25772/T8G1-H538 ; https://scholarscompass.vcu.edu/etd/3553

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


Wayne State University

27. Alla, Lakshmi Neha Reddy. An Evaluation Of Endocrine Disrupting Effects Of Emerging Contaminants Using Daphnia Pulex And Danio Rerio.

Degree: MS, Pharmaceutical Sciences, 2017, Wayne State University

  The limit of the availability of water is based on two factors, scarcity and quality. Conserving and protecting our water resources one of the… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Alla, L. N. R. (2017). An Evaluation Of Endocrine Disrupting Effects Of Emerging Contaminants Using Daphnia Pulex And Danio Rerio. (Masters Thesis). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_theses/544

Chicago Manual of Style (16th Edition):

Alla, Lakshmi Neha Reddy. “An Evaluation Of Endocrine Disrupting Effects Of Emerging Contaminants Using Daphnia Pulex And Danio Rerio.” 2017. Masters Thesis, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_theses/544.

MLA Handbook (7th Edition):

Alla, Lakshmi Neha Reddy. “An Evaluation Of Endocrine Disrupting Effects Of Emerging Contaminants Using Daphnia Pulex And Danio Rerio.” 2017. Web. 20 Sep 2020.

Vancouver:

Alla LNR. An Evaluation Of Endocrine Disrupting Effects Of Emerging Contaminants Using Daphnia Pulex And Danio Rerio. [Internet] [Masters thesis]. Wayne State University; 2017. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_theses/544.

Council of Science Editors:

Alla LNR. An Evaluation Of Endocrine Disrupting Effects Of Emerging Contaminants Using Daphnia Pulex And Danio Rerio. [Masters Thesis]. Wayne State University; 2017. Available from: https://digitalcommons.wayne.edu/oa_theses/544


Wayne State University

28. Wang, Zhaoxian. Redox Responsive Cerium Oxide Nanoparticles And Cd44 Targeted Nanomicelles For Selective Cancer Therapy.

Degree: MS, Pharmaceutical Sciences, 2017, Wayne State University

  Redox-responsive cerium oxide nanoparticles (CNPs) can play a versatile role in cancer therapy due to their ability to induce oxidative stress under proper pH… (more)

Subjects/Keywords: Pharmaceutics; Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Wang, Z. (2017). Redox Responsive Cerium Oxide Nanoparticles And Cd44 Targeted Nanomicelles For Selective Cancer Therapy. (Masters Thesis). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_theses/592

Chicago Manual of Style (16th Edition):

Wang, Zhaoxian. “Redox Responsive Cerium Oxide Nanoparticles And Cd44 Targeted Nanomicelles For Selective Cancer Therapy.” 2017. Masters Thesis, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_theses/592.

MLA Handbook (7th Edition):

Wang, Zhaoxian. “Redox Responsive Cerium Oxide Nanoparticles And Cd44 Targeted Nanomicelles For Selective Cancer Therapy.” 2017. Web. 20 Sep 2020.

Vancouver:

Wang Z. Redox Responsive Cerium Oxide Nanoparticles And Cd44 Targeted Nanomicelles For Selective Cancer Therapy. [Internet] [Masters thesis]. Wayne State University; 2017. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_theses/592.

Council of Science Editors:

Wang Z. Redox Responsive Cerium Oxide Nanoparticles And Cd44 Targeted Nanomicelles For Selective Cancer Therapy. [Masters Thesis]. Wayne State University; 2017. Available from: https://digitalcommons.wayne.edu/oa_theses/592


Wayne State University

29. Cheemalakonda, Lakshmi Deepika. Development And Evaluation Of Plga-S-S-Peg Micelles Coencapsulating Curcumin Difluorinated And Paclitaxel For Synergistic Therapeutic Efficacy.

Degree: MS, Pharmaceutical Sciences, 2014, Wayne State University

  ABSTRACT DEVELOPMENT AND EVALUATION OF PLGA-S-S-PEG MICELLES COENCAPSULATING CURCUMIN DIFLUORINATED AND PACLITAXEL FOR SYNERGISTIC THERAPEUTIC EFFICACY by LAKSHMI DEEPIKA CHEEMALAKONDA August 2014 Advisor: Dr.… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Cheemalakonda, L. D. (2014). Development And Evaluation Of Plga-S-S-Peg Micelles Coencapsulating Curcumin Difluorinated And Paclitaxel For Synergistic Therapeutic Efficacy. (Masters Thesis). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_theses/343

Chicago Manual of Style (16th Edition):

Cheemalakonda, Lakshmi Deepika. “Development And Evaluation Of Plga-S-S-Peg Micelles Coencapsulating Curcumin Difluorinated And Paclitaxel For Synergistic Therapeutic Efficacy.” 2014. Masters Thesis, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_theses/343.

MLA Handbook (7th Edition):

Cheemalakonda, Lakshmi Deepika. “Development And Evaluation Of Plga-S-S-Peg Micelles Coencapsulating Curcumin Difluorinated And Paclitaxel For Synergistic Therapeutic Efficacy.” 2014. Web. 20 Sep 2020.

Vancouver:

Cheemalakonda LD. Development And Evaluation Of Plga-S-S-Peg Micelles Coencapsulating Curcumin Difluorinated And Paclitaxel For Synergistic Therapeutic Efficacy. [Internet] [Masters thesis]. Wayne State University; 2014. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_theses/343.

Council of Science Editors:

Cheemalakonda LD. Development And Evaluation Of Plga-S-S-Peg Micelles Coencapsulating Curcumin Difluorinated And Paclitaxel For Synergistic Therapeutic Efficacy. [Masters Thesis]. Wayne State University; 2014. Available from: https://digitalcommons.wayne.edu/oa_theses/343


Wayne State University

30. Shi, Zhiwen. Site-Directed Mutagenesis Of Conserved Amino Acids Residues In N5-Carboxyaminoimidazole Ribonucleotide Mutase: Converting N5-Cair Mutase Into Aminoimidazole Ribonnucleotide Carboxylase & Developing A High-Throughput Screening Assay For The Discovery Of N5-Carboxyaminoimidazole Ribonucleotide Mutase.

Degree: MS, Pharmaceutical Sciences, 2014, Wayne State University

  The de novo purine biosynthesis pathway plays a critical role in providing new purines to the cell. Previous studies have shown differences between the… (more)

Subjects/Keywords: Medicinal Chemistry and Pharmaceutics

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

APA (6th Edition):

Shi, Z. (2014). Site-Directed Mutagenesis Of Conserved Amino Acids Residues In N5-Carboxyaminoimidazole Ribonucleotide Mutase: Converting N5-Cair Mutase Into Aminoimidazole Ribonnucleotide Carboxylase & Developing A High-Throughput Screening Assay For The Discovery Of N5-Carboxyaminoimidazole Ribonucleotide Mutase. (Masters Thesis). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_theses/354

Chicago Manual of Style (16th Edition):

Shi, Zhiwen. “Site-Directed Mutagenesis Of Conserved Amino Acids Residues In N5-Carboxyaminoimidazole Ribonucleotide Mutase: Converting N5-Cair Mutase Into Aminoimidazole Ribonnucleotide Carboxylase & Developing A High-Throughput Screening Assay For The Discovery Of N5-Carboxyaminoimidazole Ribonucleotide Mutase.” 2014. Masters Thesis, Wayne State University. Accessed September 20, 2020. https://digitalcommons.wayne.edu/oa_theses/354.

MLA Handbook (7th Edition):

Shi, Zhiwen. “Site-Directed Mutagenesis Of Conserved Amino Acids Residues In N5-Carboxyaminoimidazole Ribonucleotide Mutase: Converting N5-Cair Mutase Into Aminoimidazole Ribonnucleotide Carboxylase & Developing A High-Throughput Screening Assay For The Discovery Of N5-Carboxyaminoimidazole Ribonucleotide Mutase.” 2014. Web. 20 Sep 2020.

Vancouver:

Shi Z. Site-Directed Mutagenesis Of Conserved Amino Acids Residues In N5-Carboxyaminoimidazole Ribonucleotide Mutase: Converting N5-Cair Mutase Into Aminoimidazole Ribonnucleotide Carboxylase & Developing A High-Throughput Screening Assay For The Discovery Of N5-Carboxyaminoimidazole Ribonucleotide Mutase. [Internet] [Masters thesis]. Wayne State University; 2014. [cited 2020 Sep 20]. Available from: https://digitalcommons.wayne.edu/oa_theses/354.

Council of Science Editors:

Shi Z. Site-Directed Mutagenesis Of Conserved Amino Acids Residues In N5-Carboxyaminoimidazole Ribonucleotide Mutase: Converting N5-Cair Mutase Into Aminoimidazole Ribonnucleotide Carboxylase & Developing A High-Throughput Screening Assay For The Discovery Of N5-Carboxyaminoimidazole Ribonucleotide Mutase. [Masters Thesis]. Wayne State University; 2014. Available from: https://digitalcommons.wayne.edu/oa_theses/354

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