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You searched for subject:(small molecules). Showing records 1 – 30 of 190 total matches.

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University of Miami

1. Lopez, Christopher J. Part I. NMR Studies of Aggregation in Organic Dyes and Salts Part II. Design of Relaxation and Diffusion Selective Pulses.

Degree: PhD, Chemistry (Arts and Sciences), 2014, University of Miami

  Part I. Small organic molecules can play important medicinal roles as markers for antitumor agents, drug delivery, drug discovery, and proteins. However, many small(more)

Subjects/Keywords: Aggregation of small organic molecules

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APA (6th Edition):

Lopez, C. J. (2014). Part I. NMR Studies of Aggregation in Organic Dyes and Salts Part II. Design of Relaxation and Diffusion Selective Pulses. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/1348

Chicago Manual of Style (16th Edition):

Lopez, Christopher J. “Part I. NMR Studies of Aggregation in Organic Dyes and Salts Part II. Design of Relaxation and Diffusion Selective Pulses.” 2014. Doctoral Dissertation, University of Miami. Accessed October 27, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/1348.

MLA Handbook (7th Edition):

Lopez, Christopher J. “Part I. NMR Studies of Aggregation in Organic Dyes and Salts Part II. Design of Relaxation and Diffusion Selective Pulses.” 2014. Web. 27 Oct 2020.

Vancouver:

Lopez CJ. Part I. NMR Studies of Aggregation in Organic Dyes and Salts Part II. Design of Relaxation and Diffusion Selective Pulses. [Internet] [Doctoral dissertation]. University of Miami; 2014. [cited 2020 Oct 27]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1348.

Council of Science Editors:

Lopez CJ. Part I. NMR Studies of Aggregation in Organic Dyes and Salts Part II. Design of Relaxation and Diffusion Selective Pulses. [Doctoral Dissertation]. University of Miami; 2014. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1348


University of New South Wales

2. Bonello, Teresa. Characterising the impact of tropomyosin targeting compounds on the actin cytoskeleton.

Degree: Medical Sciences, 2013, University of New South Wales

 Targeting specific actin filament populations involved in tumour cell function represents a long-standing challenge in the area of anti-cancer drug development. The tropomyosin (Tm) family… (more)

Subjects/Keywords: Small molecules; Actin; Tropomyosin; Cancer

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APA (6th Edition):

Bonello, T. (2013). Characterising the impact of tropomyosin targeting compounds on the actin cytoskeleton. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52946 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11624/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Bonello, Teresa. “Characterising the impact of tropomyosin targeting compounds on the actin cytoskeleton.” 2013. Doctoral Dissertation, University of New South Wales. Accessed October 27, 2020. http://handle.unsw.edu.au/1959.4/52946 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11624/SOURCE01?view=true.

MLA Handbook (7th Edition):

Bonello, Teresa. “Characterising the impact of tropomyosin targeting compounds on the actin cytoskeleton.” 2013. Web. 27 Oct 2020.

Vancouver:

Bonello T. Characterising the impact of tropomyosin targeting compounds on the actin cytoskeleton. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2020 Oct 27]. Available from: http://handle.unsw.edu.au/1959.4/52946 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11624/SOURCE01?view=true.

Council of Science Editors:

Bonello T. Characterising the impact of tropomyosin targeting compounds on the actin cytoskeleton. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52946 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11624/SOURCE01?view=true

3. Wijaya, Juwina. Utilizing Small Molecules to Study Mitochondrial Presequence-Degrading Protease.

Degree: Biochemistry & Molecular Biology, 2015, UCLA

 Proper mitochondrial function contributes to cell’s health and integrity. Perturbations in mitochondrial homeostasis have been linked to diseases, specifically neurodegenerative diseases. Understanding the players of… (more)

Subjects/Keywords: Biochemistry; Chemical Biology; Mitochondria; Protease; Small molecules

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APA (6th Edition):

Wijaya, J. (2015). Utilizing Small Molecules to Study Mitochondrial Presequence-Degrading Protease. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/8nm1z5z8

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):

Wijaya, Juwina. “Utilizing Small Molecules to Study Mitochondrial Presequence-Degrading Protease.” 2015. Thesis, UCLA. Accessed October 27, 2020. http://www.escholarship.org/uc/item/8nm1z5z8.

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

MLA Handbook (7th Edition):

Wijaya, Juwina. “Utilizing Small Molecules to Study Mitochondrial Presequence-Degrading Protease.” 2015. Web. 27 Oct 2020.

Vancouver:

Wijaya J. Utilizing Small Molecules to Study Mitochondrial Presequence-Degrading Protease. [Internet] [Thesis]. UCLA; 2015. [cited 2020 Oct 27]. Available from: http://www.escholarship.org/uc/item/8nm1z5z8.

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

Council of Science Editors:

Wijaya J. Utilizing Small Molecules to Study Mitochondrial Presequence-Degrading Protease. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/8nm1z5z8

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


University of Manchester

4. Uggenti, Carolina. Modification of mutant bestrophin-1 processing to prevent retinal degeneration.

Degree: PhD, 2015, University of Manchester

 Bestrophin-1 is a homopentameric Ca2+-gated anion channel which localises to the basolateral plasma membrane of retinal pigment epithelium (RPE) cells. Homozygous and compound heterozygous mutations… (more)

Subjects/Keywords: 617.7; bestrophin-1; small molecules treatment

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APA (6th Edition):

Uggenti, C. (2015). Modification of mutant bestrophin-1 processing to prevent retinal degeneration. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/modification-of-mutant-bestrophin1-processing-to-prevent-retinal-degeneration(854430cf-9c14-4142-85f4-8f1594310c05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677814

Chicago Manual of Style (16th Edition):

Uggenti, Carolina. “Modification of mutant bestrophin-1 processing to prevent retinal degeneration.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 27, 2020. https://www.research.manchester.ac.uk/portal/en/theses/modification-of-mutant-bestrophin1-processing-to-prevent-retinal-degeneration(854430cf-9c14-4142-85f4-8f1594310c05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677814.

MLA Handbook (7th Edition):

Uggenti, Carolina. “Modification of mutant bestrophin-1 processing to prevent retinal degeneration.” 2015. Web. 27 Oct 2020.

Vancouver:

Uggenti C. Modification of mutant bestrophin-1 processing to prevent retinal degeneration. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Oct 27]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modification-of-mutant-bestrophin1-processing-to-prevent-retinal-degeneration(854430cf-9c14-4142-85f4-8f1594310c05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677814.

Council of Science Editors:

Uggenti C. Modification of mutant bestrophin-1 processing to prevent retinal degeneration. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modification-of-mutant-bestrophin1-processing-to-prevent-retinal-degeneration(854430cf-9c14-4142-85f4-8f1594310c05).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.677814

5. Zhang, Man. Design, synthesis, and evaluation of bioactive molecules; Chiral polyvinylpyrrolidones supported Cu/Au nanoclusters catalyzed cyclization of 5-substituted nona-1,8-dien-5-ols.

Degree: PhD, Department of Chemistry, 2017, Kansas State University

Small molecules are of great importance in drug discovery currently. The first three chapters discussed the design, synthesis and bio-evaluation of three different classes of… (more)

Subjects/Keywords: Bioactive small molecules; Chiral-substituted polyvinylpyrrolidones (CSPVP)

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APA (6th Edition):

Zhang, M. (2017). Design, synthesis, and evaluation of bioactive molecules; Chiral polyvinylpyrrolidones supported Cu/Au nanoclusters catalyzed cyclization of 5-substituted nona-1,8-dien-5-ols. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/35470

Chicago Manual of Style (16th Edition):

Zhang, Man. “Design, synthesis, and evaluation of bioactive molecules; Chiral polyvinylpyrrolidones supported Cu/Au nanoclusters catalyzed cyclization of 5-substituted nona-1,8-dien-5-ols.” 2017. Doctoral Dissertation, Kansas State University. Accessed October 27, 2020. http://hdl.handle.net/2097/35470.

MLA Handbook (7th Edition):

Zhang, Man. “Design, synthesis, and evaluation of bioactive molecules; Chiral polyvinylpyrrolidones supported Cu/Au nanoclusters catalyzed cyclization of 5-substituted nona-1,8-dien-5-ols.” 2017. Web. 27 Oct 2020.

Vancouver:

Zhang M. Design, synthesis, and evaluation of bioactive molecules; Chiral polyvinylpyrrolidones supported Cu/Au nanoclusters catalyzed cyclization of 5-substituted nona-1,8-dien-5-ols. [Internet] [Doctoral dissertation]. Kansas State University; 2017. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/2097/35470.

Council of Science Editors:

Zhang M. Design, synthesis, and evaluation of bioactive molecules; Chiral polyvinylpyrrolidones supported Cu/Au nanoclusters catalyzed cyclization of 5-substituted nona-1,8-dien-5-ols. [Doctoral Dissertation]. Kansas State University; 2017. Available from: http://hdl.handle.net/2097/35470


University of New South Wales

6. Mills, Toby. Diversity and bioactivity of microorganisms associated with Australian stingless bee species.

Degree: Chemistry, 2018, University of New South Wales

 The rapid emergence and transfer of antimicrobial resistance in pathogenic organisms has greatly reduced our ability to treat clinical microbial infections. To continue to treat… (more)

Subjects/Keywords: Antimicrobial; Stingless bees; Bioactive small molecules; Microbiome

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APA (6th Edition):

Mills, T. (2018). Diversity and bioactivity of microorganisms associated with Australian stingless bee species. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60350 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51889/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Mills, Toby. “Diversity and bioactivity of microorganisms associated with Australian stingless bee species.” 2018. Doctoral Dissertation, University of New South Wales. Accessed October 27, 2020. http://handle.unsw.edu.au/1959.4/60350 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51889/SOURCE02?view=true.

MLA Handbook (7th Edition):

Mills, Toby. “Diversity and bioactivity of microorganisms associated with Australian stingless bee species.” 2018. Web. 27 Oct 2020.

Vancouver:

Mills T. Diversity and bioactivity of microorganisms associated with Australian stingless bee species. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2020 Oct 27]. Available from: http://handle.unsw.edu.au/1959.4/60350 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51889/SOURCE02?view=true.

Council of Science Editors:

Mills T. Diversity and bioactivity of microorganisms associated with Australian stingless bee species. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/60350 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:51889/SOURCE02?view=true


The Ohio State University

7. Behnke, Shelby Lee. Resonance Raman Investigations of [NiFe] Hydrogenase Models.

Degree: MS, Chemistry, 2016, The Ohio State University

 Hydrogenase (H2ases) enzymes carry out bidirectional hydrogen production and oxidation reactions. To better understand the mechanism of hydrogen conversion, spectroscopic studies on small molecule mimics… (more)

Subjects/Keywords: Chemistry; Resonance Raman; Spectroscopy; Hydrogenase; small molecules

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APA (6th Edition):

Behnke, S. L. (2016). Resonance Raman Investigations of [NiFe] Hydrogenase Models. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1479728987893667

Chicago Manual of Style (16th Edition):

Behnke, Shelby Lee. “Resonance Raman Investigations of [NiFe] Hydrogenase Models.” 2016. Masters Thesis, The Ohio State University. Accessed October 27, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1479728987893667.

MLA Handbook (7th Edition):

Behnke, Shelby Lee. “Resonance Raman Investigations of [NiFe] Hydrogenase Models.” 2016. Web. 27 Oct 2020.

Vancouver:

Behnke SL. Resonance Raman Investigations of [NiFe] Hydrogenase Models. [Internet] [Masters thesis]. The Ohio State University; 2016. [cited 2020 Oct 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1479728987893667.

Council of Science Editors:

Behnke SL. Resonance Raman Investigations of [NiFe] Hydrogenase Models. [Masters Thesis]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1479728987893667


University of Edinburgh

8. Marie, Kerrie Leanne. Chemical and genetic control of melanocyte development, proliferation and regeneration in zebrafish.

Degree: PhD, 2013, University of Edinburgh

 Melanocytes are pigment-producing cells that colour our hair, skin and eyes. Melanocytes are evolutionary conserved in vertebrates, and in addition to contributing to pigmentation and… (more)

Subjects/Keywords: 616.99; zebrafish; small-molecules; small molecule screen; melanocyte; development; regeneration

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APA (6th Edition):

Marie, K. L. (2013). Chemical and genetic control of melanocyte development, proliferation and regeneration in zebrafish. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/11821

Chicago Manual of Style (16th Edition):

Marie, Kerrie Leanne. “Chemical and genetic control of melanocyte development, proliferation and regeneration in zebrafish.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed October 27, 2020. http://hdl.handle.net/1842/11821.

MLA Handbook (7th Edition):

Marie, Kerrie Leanne. “Chemical and genetic control of melanocyte development, proliferation and regeneration in zebrafish.” 2013. Web. 27 Oct 2020.

Vancouver:

Marie KL. Chemical and genetic control of melanocyte development, proliferation and regeneration in zebrafish. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1842/11821.

Council of Science Editors:

Marie KL. Chemical and genetic control of melanocyte development, proliferation and regeneration in zebrafish. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/11821

9. Yadav, Seema. Complexes of metal ion with small doner groups molecules; -.

Degree: Chemistry, 2012, Aligarh Muslim University

non

Bibliography page is at the end of each chapter.

Advisors/Committee Members: Siddiq, K.S.

Subjects/Keywords: Metal Ion; Small Doner ,; Molecules

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APA (6th Edition):

Yadav, S. (2012). Complexes of metal ion with small doner groups molecules; -. (Thesis). Aligarh Muslim University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/28616

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):

Yadav, Seema. “Complexes of metal ion with small doner groups molecules; -.” 2012. Thesis, Aligarh Muslim University. Accessed October 27, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/28616.

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

MLA Handbook (7th Edition):

Yadav, Seema. “Complexes of metal ion with small doner groups molecules; -.” 2012. Web. 27 Oct 2020.

Vancouver:

Yadav S. Complexes of metal ion with small doner groups molecules; -. [Internet] [Thesis]. Aligarh Muslim University; 2012. [cited 2020 Oct 27]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28616.

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

Council of Science Editors:

Yadav S. Complexes of metal ion with small doner groups molecules; -. [Thesis]. Aligarh Muslim University; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/28616

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

10. Del Rio, Natalia. Germylène P,N-hétérocyclique : synthèse et réactivité : P,N-heterocyclic germylene : synthesis and reactivity.

Degree: Docteur es, Chimie organométallique de coordination, 2016, Université Toulouse III – Paul Sabatier

Ce travail de thèse est axé sur la synthèse et la réactivité d'un nouveau germylène P,N-hétérocyclique stabilisé par un fragment phosphanylidène-phosphorane. Le premier chapitre constitue… (more)

Subjects/Keywords: Germylène; Réactivité; Petites molécules; Germylene; Reactivity; Small molecules

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APA (6th Edition):

Del Rio, N. (2016). Germylène P,N-hétérocyclique : synthèse et réactivité : P,N-heterocyclic germylene : synthesis and reactivity. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2016TOU30319

Chicago Manual of Style (16th Edition):

Del Rio, Natalia. “Germylène P,N-hétérocyclique : synthèse et réactivité : P,N-heterocyclic germylene : synthesis and reactivity.” 2016. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed October 27, 2020. http://www.theses.fr/2016TOU30319.

MLA Handbook (7th Edition):

Del Rio, Natalia. “Germylène P,N-hétérocyclique : synthèse et réactivité : P,N-heterocyclic germylene : synthesis and reactivity.” 2016. Web. 27 Oct 2020.

Vancouver:

Del Rio N. Germylène P,N-hétérocyclique : synthèse et réactivité : P,N-heterocyclic germylene : synthesis and reactivity. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2016. [cited 2020 Oct 27]. Available from: http://www.theses.fr/2016TOU30319.

Council of Science Editors:

Del Rio N. Germylène P,N-hétérocyclique : synthèse et réactivité : P,N-heterocyclic germylene : synthesis and reactivity. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2016. Available from: http://www.theses.fr/2016TOU30319


UCLA

11. Douglas, Colin Joseph. Investigation and Characterization of Small Molecule Modulators for Mitochondrial Processing Peptidase.

Degree: Biochemistry & Molecular Biology, 2014, UCLA

 Mitochondria are an extremely complex organelle comprised of four discrete compartments and are vital for the proper functioning of key cellular pathways including, energy production,… (more)

Subjects/Keywords: Biochemistry; high throughput screen; mitochondria; mitochondrial import; MPP; small molecules; zebrafish

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APA (6th Edition):

Douglas, C. J. (2014). Investigation and Characterization of Small Molecule Modulators for Mitochondrial Processing Peptidase. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9th259qj

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):

Douglas, Colin Joseph. “Investigation and Characterization of Small Molecule Modulators for Mitochondrial Processing Peptidase.” 2014. Thesis, UCLA. Accessed October 27, 2020. http://www.escholarship.org/uc/item/9th259qj.

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

MLA Handbook (7th Edition):

Douglas, Colin Joseph. “Investigation and Characterization of Small Molecule Modulators for Mitochondrial Processing Peptidase.” 2014. Web. 27 Oct 2020.

Vancouver:

Douglas CJ. Investigation and Characterization of Small Molecule Modulators for Mitochondrial Processing Peptidase. [Internet] [Thesis]. UCLA; 2014. [cited 2020 Oct 27]. Available from: http://www.escholarship.org/uc/item/9th259qj.

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

Council of Science Editors:

Douglas CJ. Investigation and Characterization of Small Molecule Modulators for Mitochondrial Processing Peptidase. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/9th259qj

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


University of Rochester

12. Ofori, Leslie Odame (1980 - ). Solving the problem of sequence selective RNA recognition by small molecules with application to Myotonic Dystrophy and HIV.

Degree: PhD, 2013, University of Rochester

 Synthetic small molecules that bind specific RNA sequences with high affinity are essential biochemical probes for understanding cellular process and as therapeutic agents for treatment… (more)

Subjects/Keywords: Binding constant; Myotonic Dystrophy; RNA; Small molecules; Selectivity

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APA (6th Edition):

Ofori, L. O. (. -. ). (2013). Solving the problem of sequence selective RNA recognition by small molecules with application to Myotonic Dystrophy and HIV. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/26491

Chicago Manual of Style (16th Edition):

Ofori, Leslie Odame (1980 - ). “Solving the problem of sequence selective RNA recognition by small molecules with application to Myotonic Dystrophy and HIV.” 2013. Doctoral Dissertation, University of Rochester. Accessed October 27, 2020. http://hdl.handle.net/1802/26491.

MLA Handbook (7th Edition):

Ofori, Leslie Odame (1980 - ). “Solving the problem of sequence selective RNA recognition by small molecules with application to Myotonic Dystrophy and HIV.” 2013. Web. 27 Oct 2020.

Vancouver:

Ofori LO(-). Solving the problem of sequence selective RNA recognition by small molecules with application to Myotonic Dystrophy and HIV. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1802/26491.

Council of Science Editors:

Ofori LO(-). Solving the problem of sequence selective RNA recognition by small molecules with application to Myotonic Dystrophy and HIV. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/26491


University of Alberta

13. Chu, Carmen Y.S. Rescue of Kidney Anion Exchanger 1 Trafficking Mutants.

Degree: MS, Department of Physiology, 2012, University of Alberta

 The kidney anion exchanger 1 (kAE1) is crucial in the regulation of physiological pH by facilitating Cl-/HCO3- exchange. Inability to do so results in distal… (more)

Subjects/Keywords: Trafficking; Anion Exchanger; Degradation; Rescue; Chemicals; Small molecules; Kidney

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APA (6th Edition):

Chu, C. Y. S. (2012). Rescue of Kidney Anion Exchanger 1 Trafficking Mutants. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/xs55md05p

Chicago Manual of Style (16th Edition):

Chu, Carmen Y S. “Rescue of Kidney Anion Exchanger 1 Trafficking Mutants.” 2012. Masters Thesis, University of Alberta. Accessed October 27, 2020. https://era.library.ualberta.ca/files/xs55md05p.

MLA Handbook (7th Edition):

Chu, Carmen Y S. “Rescue of Kidney Anion Exchanger 1 Trafficking Mutants.” 2012. Web. 27 Oct 2020.

Vancouver:

Chu CYS. Rescue of Kidney Anion Exchanger 1 Trafficking Mutants. [Internet] [Masters thesis]. University of Alberta; 2012. [cited 2020 Oct 27]. Available from: https://era.library.ualberta.ca/files/xs55md05p.

Council of Science Editors:

Chu CYS. Rescue of Kidney Anion Exchanger 1 Trafficking Mutants. [Masters Thesis]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/xs55md05p


University of Michigan

14. Wong, Jenny-Marie. Liquid Chromatography-Mass Spectrometry Strategies for in vivo Neurochemical Monitoring with Microdialysis.

Degree: PhD, Chemistry, 2016, University of Michigan

 Liquid chromatography mass spectrometry (LC-MS) is a powerful analytical tool for multi-analyte quantification. This method can be combined with microdialysis sampling to study small molecules(more)

Subjects/Keywords: liquid chromatography mass spectrometry neuropeptides and small molecules; Chemistry; Science

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APA (6th Edition):

Wong, J. (2016). Liquid Chromatography-Mass Spectrometry Strategies for in vivo Neurochemical Monitoring with Microdialysis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/135792

Chicago Manual of Style (16th Edition):

Wong, Jenny-Marie. “Liquid Chromatography-Mass Spectrometry Strategies for in vivo Neurochemical Monitoring with Microdialysis.” 2016. Doctoral Dissertation, University of Michigan. Accessed October 27, 2020. http://hdl.handle.net/2027.42/135792.

MLA Handbook (7th Edition):

Wong, Jenny-Marie. “Liquid Chromatography-Mass Spectrometry Strategies for in vivo Neurochemical Monitoring with Microdialysis.” 2016. Web. 27 Oct 2020.

Vancouver:

Wong J. Liquid Chromatography-Mass Spectrometry Strategies for in vivo Neurochemical Monitoring with Microdialysis. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/2027.42/135792.

Council of Science Editors:

Wong J. Liquid Chromatography-Mass Spectrometry Strategies for in vivo Neurochemical Monitoring with Microdialysis. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/135792


Vanderbilt University

15. Cross, Emily Elizabeth. Studies on the Molecular Regulation of Epicardial Cell Movement.

Degree: PhD, Cell and Developmental Biology, 2012, Vanderbilt University

 Epicardial development is a complex process that involves tightly regulated coordination of concurrent cellular behaviors ranging from sheet migration to secretion. The regulation of these… (more)

Subjects/Keywords: Small Organic Molecules; NDRG4; Bves; migration; cell biology; heart

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APA (6th Edition):

Cross, E. E. (2012). Studies on the Molecular Regulation of Epicardial Cell Movement. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10483

Chicago Manual of Style (16th Edition):

Cross, Emily Elizabeth. “Studies on the Molecular Regulation of Epicardial Cell Movement.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed October 27, 2020. http://hdl.handle.net/1803/10483.

MLA Handbook (7th Edition):

Cross, Emily Elizabeth. “Studies on the Molecular Regulation of Epicardial Cell Movement.” 2012. Web. 27 Oct 2020.

Vancouver:

Cross EE. Studies on the Molecular Regulation of Epicardial Cell Movement. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1803/10483.

Council of Science Editors:

Cross EE. Studies on the Molecular Regulation of Epicardial Cell Movement. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/10483


Vanderbilt University

16. Williams, Charles Houston III. Chemical genetics of Vertebrate development.

Degree: PhD, Cell and Developmental Biology, 2017, Vanderbilt University

Small molecules have value in their ability to modulate protein activity in ways that are not accessible using conventional genetic methods, and their potential to… (more)

Subjects/Keywords: Signalling pathways; Developmental Biology; Chemical Biology; small molecules

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APA (6th Edition):

Williams, C. H. I. (2017). Chemical genetics of Vertebrate development. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10641

Chicago Manual of Style (16th Edition):

Williams, Charles Houston III. “Chemical genetics of Vertebrate development.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed October 27, 2020. http://hdl.handle.net/1803/10641.

MLA Handbook (7th Edition):

Williams, Charles Houston III. “Chemical genetics of Vertebrate development.” 2017. Web. 27 Oct 2020.

Vancouver:

Williams CHI. Chemical genetics of Vertebrate development. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1803/10641.

Council of Science Editors:

Williams CHI. Chemical genetics of Vertebrate development. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/10641


Penn State University

17. Ramadoss, Nitya S. The trans-translation pathway as a target for broad-spectrum antibacterial development.

Degree: 2013, Penn State University

 One of many current, pressing concerns on a global scale regarding public health, is the emergence of multi-drug resistant pathogens that cause a number of… (more)

Subjects/Keywords: trans-translation; tmRNA; antibiotic development; small molecules; Shigella flexneri

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APA (6th Edition):

Ramadoss, N. S. (2013). The trans-translation pathway as a target for broad-spectrum antibacterial development. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/17352

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):

Ramadoss, Nitya S. “The trans-translation pathway as a target for broad-spectrum antibacterial development.” 2013. Thesis, Penn State University. Accessed October 27, 2020. https://submit-etda.libraries.psu.edu/catalog/17352.

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

MLA Handbook (7th Edition):

Ramadoss, Nitya S. “The trans-translation pathway as a target for broad-spectrum antibacterial development.” 2013. Web. 27 Oct 2020.

Vancouver:

Ramadoss NS. The trans-translation pathway as a target for broad-spectrum antibacterial development. [Internet] [Thesis]. Penn State University; 2013. [cited 2020 Oct 27]. Available from: https://submit-etda.libraries.psu.edu/catalog/17352.

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

Council of Science Editors:

Ramadoss NS. The trans-translation pathway as a target for broad-spectrum antibacterial development. [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/17352

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


Penn State University

18. Hernandez Borrero, Liz Janice. Anti-tumor effect and destabilization of mutant p53 by CB002, a p53-pathway restoring small molecule that stimulates autophagy.

Degree: 2016, Penn State University

 Tumor suppressor p53 mediates genotoxic and cellular stress signals by controlling cell fate through transcriptional activation of genes involved in DNA repair, cell cycle arrest,… (more)

Subjects/Keywords: mutant p53; apoptosis; autophagy; p53 pathway restoration; small molecules; NOXA

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APA (6th Edition):

Hernandez Borrero, L. J. (2016). Anti-tumor effect and destabilization of mutant p53 by CB002, a p53-pathway restoring small molecule that stimulates autophagy. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13038ljh216

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):

Hernandez Borrero, Liz Janice. “Anti-tumor effect and destabilization of mutant p53 by CB002, a p53-pathway restoring small molecule that stimulates autophagy.” 2016. Thesis, Penn State University. Accessed October 27, 2020. https://submit-etda.libraries.psu.edu/catalog/13038ljh216.

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

MLA Handbook (7th Edition):

Hernandez Borrero, Liz Janice. “Anti-tumor effect and destabilization of mutant p53 by CB002, a p53-pathway restoring small molecule that stimulates autophagy.” 2016. Web. 27 Oct 2020.

Vancouver:

Hernandez Borrero LJ. Anti-tumor effect and destabilization of mutant p53 by CB002, a p53-pathway restoring small molecule that stimulates autophagy. [Internet] [Thesis]. Penn State University; 2016. [cited 2020 Oct 27]. Available from: https://submit-etda.libraries.psu.edu/catalog/13038ljh216.

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

Council of Science Editors:

Hernandez Borrero LJ. Anti-tumor effect and destabilization of mutant p53 by CB002, a p53-pathway restoring small molecule that stimulates autophagy. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/13038ljh216

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


University of California – Berkeley

19. Sia, Junren. Influencing cell fate decisions using physical and chemical cues.

Degree: Bioengineering, 2016, University of California – Berkeley

 Directed genetic reprogramming of cells from one identity to another offers tremendous potential in regenerative medicine, disease modelling and drug testing. However, its application is… (more)

Subjects/Keywords: Biology; Cardiomyocyte; iPSC; Mechanotransduction; Reprogramming; Skeletal muscle; Small molecules

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APA (6th Edition):

Sia, J. (2016). Influencing cell fate decisions using physical and chemical cues. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0bq39484

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):

Sia, Junren. “Influencing cell fate decisions using physical and chemical cues.” 2016. Thesis, University of California – Berkeley. Accessed October 27, 2020. http://www.escholarship.org/uc/item/0bq39484.

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

MLA Handbook (7th Edition):

Sia, Junren. “Influencing cell fate decisions using physical and chemical cues.” 2016. Web. 27 Oct 2020.

Vancouver:

Sia J. Influencing cell fate decisions using physical and chemical cues. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Oct 27]. Available from: http://www.escholarship.org/uc/item/0bq39484.

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

Council of Science Editors:

Sia J. Influencing cell fate decisions using physical and chemical cues. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/0bq39484

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

20. Ngom, Mor. Small molecule stimulators for enhanced yield of human hematopoietic stem cells : Petites molecules stimulatrices pour un rendement accru en cellules souches hématopoietiques humaines.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie. Hématologie, 2017, Sorbonne Paris Cité

Une transduction efficace des cellules souches hematopoïetiques est un préalable pour la thérapie génique des maladies génétiques comme la β‐thalassemie, l’Adrenoleucodystrophie et le Déficit Immunitaire… (more)

Subjects/Keywords: Petite molécule UM171; Vecteurs lentiviraux; Small molecules UM171; Lentiviral vectors

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APA (6th Edition):

Ngom, M. (2017). Small molecule stimulators for enhanced yield of human hematopoietic stem cells : Petites molecules stimulatrices pour un rendement accru en cellules souches hématopoietiques humaines. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC320

Chicago Manual of Style (16th Edition):

Ngom, Mor. “Small molecule stimulators for enhanced yield of human hematopoietic stem cells : Petites molecules stimulatrices pour un rendement accru en cellules souches hématopoietiques humaines.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 27, 2020. http://www.theses.fr/2017USPCC320.

MLA Handbook (7th Edition):

Ngom, Mor. “Small molecule stimulators for enhanced yield of human hematopoietic stem cells : Petites molecules stimulatrices pour un rendement accru en cellules souches hématopoietiques humaines.” 2017. Web. 27 Oct 2020.

Vancouver:

Ngom M. Small molecule stimulators for enhanced yield of human hematopoietic stem cells : Petites molecules stimulatrices pour un rendement accru en cellules souches hématopoietiques humaines. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2020 Oct 27]. Available from: http://www.theses.fr/2017USPCC320.

Council of Science Editors:

Ngom M. Small molecule stimulators for enhanced yield of human hematopoietic stem cells : Petites molecules stimulatrices pour un rendement accru en cellules souches hématopoietiques humaines. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC320


Washington State University

21. [No author]. DEVELOPMENT OF PSMA-TARGETED SPECT IMAGING AGENTS FOR PROSTATE CANCER .

Degree: 2012, Washington State University

 The cell-surface enzyme prostate-specific membrane antigen (PSMA) is up-regulated and strongly expressed on prostate cancer cells associated with high grade primary, androgen independent and metastatic… (more)

Subjects/Keywords: Organic chemistry; Prostate Cancer; PSMA; Radio-imaging; small molecules

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APA (6th Edition):

author], [. (2012). DEVELOPMENT OF PSMA-TARGETED SPECT IMAGING AGENTS FOR PROSTATE CANCER . (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/4266

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):

author], [No. “DEVELOPMENT OF PSMA-TARGETED SPECT IMAGING AGENTS FOR PROSTATE CANCER .” 2012. Thesis, Washington State University. Accessed October 27, 2020. http://hdl.handle.net/2376/4266.

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

MLA Handbook (7th Edition):

author], [No. “DEVELOPMENT OF PSMA-TARGETED SPECT IMAGING AGENTS FOR PROSTATE CANCER .” 2012. Web. 27 Oct 2020.

Vancouver:

author] [. DEVELOPMENT OF PSMA-TARGETED SPECT IMAGING AGENTS FOR PROSTATE CANCER . [Internet] [Thesis]. Washington State University; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/2376/4266.

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

Council of Science Editors:

author] [. DEVELOPMENT OF PSMA-TARGETED SPECT IMAGING AGENTS FOR PROSTATE CANCER . [Thesis]. Washington State University; 2012. Available from: http://hdl.handle.net/2376/4266

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


University of Vermont

22. Heaslip, Aoife. Identification of Small Molecule Effectors of the Toxoplasma.

Degree: PhD, Cell and Molecular Biology, 2008, University of Vermont

 Toxoplasma gondii is an obligate intracellular parasite that can cause lifethreatening disease in immunocompromised individuals. Host cell invasion is therefore central to the pathology of… (more)

Subjects/Keywords: toxoplasma gondii; myosin; small-molecules

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APA (6th Edition):

Heaslip, A. (2008). Identification of Small Molecule Effectors of the Toxoplasma. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/105

Chicago Manual of Style (16th Edition):

Heaslip, Aoife. “Identification of Small Molecule Effectors of the Toxoplasma.” 2008. Doctoral Dissertation, University of Vermont. Accessed October 27, 2020. https://scholarworks.uvm.edu/graddis/105.

MLA Handbook (7th Edition):

Heaslip, Aoife. “Identification of Small Molecule Effectors of the Toxoplasma.” 2008. Web. 27 Oct 2020.

Vancouver:

Heaslip A. Identification of Small Molecule Effectors of the Toxoplasma. [Internet] [Doctoral dissertation]. University of Vermont; 2008. [cited 2020 Oct 27]. Available from: https://scholarworks.uvm.edu/graddis/105.

Council of Science Editors:

Heaslip A. Identification of Small Molecule Effectors of the Toxoplasma. [Doctoral Dissertation]. University of Vermont; 2008. Available from: https://scholarworks.uvm.edu/graddis/105


Harvard University

23. Garcia-Rivera, Enrique Miguel. Probing Synovial Sarcomas and the Ubiquitin-Proteasome System With Small Molecules.

Degree: PhD, 2017, Harvard University

Chemical probes have radically transformed our ability to modulate cellular activity by providing robust and reversible disruption of select biological processes. To uncover a novel… (more)

Subjects/Keywords: small molecules; synovial sarcomas; MET; ubiquitin; proteasome; inhibitors; chemical probes

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APA (6th Edition):

Garcia-Rivera, E. M. (2017). Probing Synovial Sarcomas and the Ubiquitin-Proteasome System With Small Molecules. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141313

Chicago Manual of Style (16th Edition):

Garcia-Rivera, Enrique Miguel. “Probing Synovial Sarcomas and the Ubiquitin-Proteasome System With Small Molecules.” 2017. Doctoral Dissertation, Harvard University. Accessed October 27, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141313.

MLA Handbook (7th Edition):

Garcia-Rivera, Enrique Miguel. “Probing Synovial Sarcomas and the Ubiquitin-Proteasome System With Small Molecules.” 2017. Web. 27 Oct 2020.

Vancouver:

Garcia-Rivera EM. Probing Synovial Sarcomas and the Ubiquitin-Proteasome System With Small Molecules. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2020 Oct 27]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141313.

Council of Science Editors:

Garcia-Rivera EM. Probing Synovial Sarcomas and the Ubiquitin-Proteasome System With Small Molecules. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141313


Harvard University

24. Shaw, Katharin. A Chemical Biology Platform to Develop Small Molecule Probes for Bromodomains.

Degree: PhD, 2017, Harvard University

Bromodomain epigenetic reader proteins play crucial roles in the pathogenesis of diseases ranging from inflammation to cancer. Small molecule inihibitors have engendered a nuanced understanding… (more)

Subjects/Keywords: chemical biology; assay development; bromodomains; epigenetics; inhibition; small molecules

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APA (6th Edition):

Shaw, K. (2017). A Chemical Biology Platform to Develop Small Molecule Probes for Bromodomains. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41142078

Chicago Manual of Style (16th Edition):

Shaw, Katharin. “A Chemical Biology Platform to Develop Small Molecule Probes for Bromodomains.” 2017. Doctoral Dissertation, Harvard University. Accessed October 27, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41142078.

MLA Handbook (7th Edition):

Shaw, Katharin. “A Chemical Biology Platform to Develop Small Molecule Probes for Bromodomains.” 2017. Web. 27 Oct 2020.

Vancouver:

Shaw K. A Chemical Biology Platform to Develop Small Molecule Probes for Bromodomains. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2020 Oct 27]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41142078.

Council of Science Editors:

Shaw K. A Chemical Biology Platform to Develop Small Molecule Probes for Bromodomains. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41142078


Eastern Michigan University

25. Weerakoon, Darshani Avanthi. Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1.

Degree: MS, Chemistry, 2014, Eastern Michigan University

  Plasminogen activator inhibitor type-1 (PAI-1) is a member of the serine protease inhibitor (serpin) superfamily. Excessive levels of PAI-1 inhibit urokinase-type plasminogen activator (uPA)… (more)

Subjects/Keywords: Drug design; Drug synthesis; Isatin; Oxindole; PAI-1; Small molecules; Chemistry

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APA (6th Edition):

Weerakoon, D. A. (2014). Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1. (Masters Thesis). Eastern Michigan University. Retrieved from https://commons.emich.edu/theses/705

Chicago Manual of Style (16th Edition):

Weerakoon, Darshani Avanthi. “Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1.” 2014. Masters Thesis, Eastern Michigan University. Accessed October 27, 2020. https://commons.emich.edu/theses/705.

MLA Handbook (7th Edition):

Weerakoon, Darshani Avanthi. “Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1.” 2014. Web. 27 Oct 2020.

Vancouver:

Weerakoon DA. Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1. [Internet] [Masters thesis]. Eastern Michigan University; 2014. [cited 2020 Oct 27]. Available from: https://commons.emich.edu/theses/705.

Council of Science Editors:

Weerakoon DA. Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1. [Masters Thesis]. Eastern Michigan University; 2014. Available from: https://commons.emich.edu/theses/705


University of California – Berkeley

26. Soto, Jennifer. Biochemical and Biophysical Regulation of Cell Reprogramming.

Degree: Bioengineering, 2016, University of California – Berkeley

 Cell reprogramming, the reverse process of differentiation, represents a major advancement in cell biology and has wide applications in regenerative medicine, drug screening and disease… (more)

Subjects/Keywords: Biomedical engineering; cell reprogramming; cytoskeleton; direct conversion; microgrooves; nanofibers; small molecules

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APA (6th Edition):

Soto, J. (2016). Biochemical and Biophysical Regulation of Cell Reprogramming. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/81n7s6pv

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):

Soto, Jennifer. “Biochemical and Biophysical Regulation of Cell Reprogramming.” 2016. Thesis, University of California – Berkeley. Accessed October 27, 2020. http://www.escholarship.org/uc/item/81n7s6pv.

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

MLA Handbook (7th Edition):

Soto, Jennifer. “Biochemical and Biophysical Regulation of Cell Reprogramming.” 2016. Web. 27 Oct 2020.

Vancouver:

Soto J. Biochemical and Biophysical Regulation of Cell Reprogramming. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Oct 27]. Available from: http://www.escholarship.org/uc/item/81n7s6pv.

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

Council of Science Editors:

Soto J. Biochemical and Biophysical Regulation of Cell Reprogramming. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/81n7s6pv

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


National University of Ireland – Galway

27. Negi, Arvind. Investigation of various ligand design approaches and synthesis of diverse heterocyclic bioactive compounds .

Degree: 2019, National University of Ireland – Galway

 Structure-based design and ligand-based design are one of the most common approaches used to develop new inhibitors against druggable protein targets in various human disorders.… (more)

Subjects/Keywords: Drug design; Synthesis; Small molecules; Apoptosis; Chemistry; Science

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APA (6th Edition):

Negi, A. (2019). Investigation of various ligand design approaches and synthesis of diverse heterocyclic bioactive compounds . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/15468

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):

Negi, Arvind. “Investigation of various ligand design approaches and synthesis of diverse heterocyclic bioactive compounds .” 2019. Thesis, National University of Ireland – Galway. Accessed October 27, 2020. http://hdl.handle.net/10379/15468.

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

MLA Handbook (7th Edition):

Negi, Arvind. “Investigation of various ligand design approaches and synthesis of diverse heterocyclic bioactive compounds .” 2019. Web. 27 Oct 2020.

Vancouver:

Negi A. Investigation of various ligand design approaches and synthesis of diverse heterocyclic bioactive compounds . [Internet] [Thesis]. National University of Ireland – Galway; 2019. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10379/15468.

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

Council of Science Editors:

Negi A. Investigation of various ligand design approaches and synthesis of diverse heterocyclic bioactive compounds . [Thesis]. National University of Ireland – Galway; 2019. Available from: http://hdl.handle.net/10379/15468

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


University of Oregon

28. Coonrod, Leslie. Targeting Myotonic Dystrophy with Small Molecules.

Degree: 2012, University of Oregon

 Myotonic dystrophy (DM) is one of the most common forms of muscular dystrophy, characterized by its hallmark symptom myotonia. DM is an autosomal dominant disease… (more)

Subjects/Keywords: CUG repeats; Myotonic dystrophy; RNA structure; Small molecules; Toxic RNA

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APA (6th Edition):

Coonrod, L. (2012). Targeting Myotonic Dystrophy with Small Molecules. (Thesis). University of Oregon. Retrieved from http://hdl.handle.net/1794/12379

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):

Coonrod, Leslie. “Targeting Myotonic Dystrophy with Small Molecules.” 2012. Thesis, University of Oregon. Accessed October 27, 2020. http://hdl.handle.net/1794/12379.

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

MLA Handbook (7th Edition):

Coonrod, Leslie. “Targeting Myotonic Dystrophy with Small Molecules.” 2012. Web. 27 Oct 2020.

Vancouver:

Coonrod L. Targeting Myotonic Dystrophy with Small Molecules. [Internet] [Thesis]. University of Oregon; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1794/12379.

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

Council of Science Editors:

Coonrod L. Targeting Myotonic Dystrophy with Small Molecules. [Thesis]. University of Oregon; 2012. Available from: http://hdl.handle.net/1794/12379

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


University of Toronto

29. Goodreid, Jordan D. Synthesis and Biological Evaluation of Antibacterial Small Molecule Activators of Caseinolytic Protease P and the Synthetic Utility of Metal Carboxylate Salts in Amidation Reactions with Amines.

Degree: PhD, 2016, University of Toronto

 This thesis is presented in two parts and summarizes work carried out in the laboratory of Professor Robert A. Batey at the University of Toronto… (more)

Subjects/Keywords: Amidation; Antibacterial; Carboxylate Salts; Depsipeptides; Small Molecules; Synthesis; 0490

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APA (6th Edition):

Goodreid, J. D. (2016). Synthesis and Biological Evaluation of Antibacterial Small Molecule Activators of Caseinolytic Protease P and the Synthetic Utility of Metal Carboxylate Salts in Amidation Reactions with Amines. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/76441

Chicago Manual of Style (16th Edition):

Goodreid, Jordan D. “Synthesis and Biological Evaluation of Antibacterial Small Molecule Activators of Caseinolytic Protease P and the Synthetic Utility of Metal Carboxylate Salts in Amidation Reactions with Amines.” 2016. Doctoral Dissertation, University of Toronto. Accessed October 27, 2020. http://hdl.handle.net/1807/76441.

MLA Handbook (7th Edition):

Goodreid, Jordan D. “Synthesis and Biological Evaluation of Antibacterial Small Molecule Activators of Caseinolytic Protease P and the Synthetic Utility of Metal Carboxylate Salts in Amidation Reactions with Amines.” 2016. Web. 27 Oct 2020.

Vancouver:

Goodreid JD. Synthesis and Biological Evaluation of Antibacterial Small Molecule Activators of Caseinolytic Protease P and the Synthetic Utility of Metal Carboxylate Salts in Amidation Reactions with Amines. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1807/76441.

Council of Science Editors:

Goodreid JD. Synthesis and Biological Evaluation of Antibacterial Small Molecule Activators of Caseinolytic Protease P and the Synthetic Utility of Metal Carboxylate Salts in Amidation Reactions with Amines. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76441


University of Toronto

30. Cheng, Xinran. Development of Biosensors to Monitor the Interaction of Small Molecules with Amyloidogenic Proteins using Optical and Electrochemical Methods.

Degree: PhD, 2015, University of Toronto

 Amyloidogenic protein fibrils are well known pathological hallmark of neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD). The Amyloid Cascade Hypothesis attributes… (more)

Subjects/Keywords: aggregation; amyloid; biosensor; electrochemistry; optical; small molecules; 0485

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

APA (6th Edition):

Cheng, X. (2015). Development of Biosensors to Monitor the Interaction of Small Molecules with Amyloidogenic Proteins using Optical and Electrochemical Methods. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/69263

Chicago Manual of Style (16th Edition):

Cheng, Xinran. “Development of Biosensors to Monitor the Interaction of Small Molecules with Amyloidogenic Proteins using Optical and Electrochemical Methods.” 2015. Doctoral Dissertation, University of Toronto. Accessed October 27, 2020. http://hdl.handle.net/1807/69263.

MLA Handbook (7th Edition):

Cheng, Xinran. “Development of Biosensors to Monitor the Interaction of Small Molecules with Amyloidogenic Proteins using Optical and Electrochemical Methods.” 2015. Web. 27 Oct 2020.

Vancouver:

Cheng X. Development of Biosensors to Monitor the Interaction of Small Molecules with Amyloidogenic Proteins using Optical and Electrochemical Methods. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1807/69263.

Council of Science Editors:

Cheng X. Development of Biosensors to Monitor the Interaction of Small Molecules with Amyloidogenic Proteins using Optical and Electrochemical Methods. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69263

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