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You searched for subject:(High throughput drug screen). Showing records 1 – 30 of 45810 total matches.

[1] [2] [3] [4] [5] … [1527]

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Vanderbilt University

1. Raphemot, Rene. Of Mosquitoes and Men: Targeting Inward Rectifier Potassium (Kir) Channels for the Development of New Therapeutics and Insecticides.

Degree: PhD, Pharmacology, 2014, Vanderbilt University

 Inward rectifier potassium (Kir) channels are a family of two transmembrane-spanning potassium selective ion channels. Kir channels are found in all kingdoms of life where… (more)

Subjects/Keywords: drug discovery; electrophysiology; thallium flux; Kir channels; pharmacology; high-throughput screen

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

APA (6th Edition):

Raphemot, R. (2014). Of Mosquitoes and Men: Targeting Inward Rectifier Potassium (Kir) Channels for the Development of New Therapeutics and Insecticides. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12336

Chicago Manual of Style (16th Edition):

Raphemot, Rene. “Of Mosquitoes and Men: Targeting Inward Rectifier Potassium (Kir) Channels for the Development of New Therapeutics and Insecticides.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed January 20, 2021. http://hdl.handle.net/1803/12336.

MLA Handbook (7th Edition):

Raphemot, Rene. “Of Mosquitoes and Men: Targeting Inward Rectifier Potassium (Kir) Channels for the Development of New Therapeutics and Insecticides.” 2014. Web. 20 Jan 2021.

Vancouver:

Raphemot R. Of Mosquitoes and Men: Targeting Inward Rectifier Potassium (Kir) Channels for the Development of New Therapeutics and Insecticides. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1803/12336.

Council of Science Editors:

Raphemot R. Of Mosquitoes and Men: Targeting Inward Rectifier Potassium (Kir) Channels for the Development of New Therapeutics and Insecticides. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/12336


University of Texas – Austin

2. Devkota, Ashwini Kumar. Mechanistic studies and drug discovery for eEF-2 kinase.

Degree: PhD, Cell and Molecular Biology, 2011, University of Texas – Austin

 eEF-2K, also known as CaM kinase-III, is an atypical protein kinase which negatively regulates the global rate of protein synthesis through the phosphorylation and inactivation… (more)

Subjects/Keywords: eEF-2 kinase; eEF-2K; Cancer; High-throughput screen; Drug discovery

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APA (6th Edition):

Devkota, A. K. (2011). Mechanistic studies and drug discovery for eEF-2 kinase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/22246

Chicago Manual of Style (16th Edition):

Devkota, Ashwini Kumar. “Mechanistic studies and drug discovery for eEF-2 kinase.” 2011. Doctoral Dissertation, University of Texas – Austin. Accessed January 20, 2021. http://hdl.handle.net/2152/22246.

MLA Handbook (7th Edition):

Devkota, Ashwini Kumar. “Mechanistic studies and drug discovery for eEF-2 kinase.” 2011. Web. 20 Jan 2021.

Vancouver:

Devkota AK. Mechanistic studies and drug discovery for eEF-2 kinase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2011. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/2152/22246.

Council of Science Editors:

Devkota AK. Mechanistic studies and drug discovery for eEF-2 kinase. [Doctoral Dissertation]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/22246


University of Toronto

3. Pacheco, Shaun. Nanoscale formulation strategy for therapeutic agents in the prevention of acute lung injury.

Degree: 2014, University of Toronto

Acute lung injury is a morbid complication with numerous causes and currently no effective clinical treatment. Studies have shown that Src protein tyrosine kinases (PTK's)… (more)

Subjects/Keywords: Acute lung injury; Drug delivery; High-throughput screen; Hydrophobic drug; Nanotechnology; Self-assembling peptide; 0719

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APA (6th Edition):

Pacheco, S. (2014). Nanoscale formulation strategy for therapeutic agents in the prevention of acute lung injury. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/69966

Chicago Manual of Style (16th Edition):

Pacheco, Shaun. “Nanoscale formulation strategy for therapeutic agents in the prevention of acute lung injury.” 2014. Masters Thesis, University of Toronto. Accessed January 20, 2021. http://hdl.handle.net/1807/69966.

MLA Handbook (7th Edition):

Pacheco, Shaun. “Nanoscale formulation strategy for therapeutic agents in the prevention of acute lung injury.” 2014. Web. 20 Jan 2021.

Vancouver:

Pacheco S. Nanoscale formulation strategy for therapeutic agents in the prevention of acute lung injury. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1807/69966.

Council of Science Editors:

Pacheco S. Nanoscale formulation strategy for therapeutic agents in the prevention of acute lung injury. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/69966


University of New South Wales

4. Khoo, Poh Sim. Molecular analysis of insulin action using high throughput genetic screens.

Degree: Clinical School - St Vincent's Hospital, 2011, University of New South Wales

 The insulin-stimulated uptake of glucose by muscle and adipose is vital for the maintenance of glucosehomeostasis in the body. This uptake primarily occurs through the… (more)

Subjects/Keywords: High throughput screen; Insulin; GLUT4

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APA (6th Edition):

Khoo, P. S. (2011). Molecular analysis of insulin action using high throughput genetic screens. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10337/SOURCE2?view=true

Chicago Manual of Style (16th Edition):

Khoo, Poh Sim. “Molecular analysis of insulin action using high throughput genetic screens.” 2011. Doctoral Dissertation, University of New South Wales. Accessed January 20, 2021. http://handle.unsw.edu.au/1959.4/51670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10337/SOURCE2?view=true.

MLA Handbook (7th Edition):

Khoo, Poh Sim. “Molecular analysis of insulin action using high throughput genetic screens.” 2011. Web. 20 Jan 2021.

Vancouver:

Khoo PS. Molecular analysis of insulin action using high throughput genetic screens. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2021 Jan 20]. Available from: http://handle.unsw.edu.au/1959.4/51670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10337/SOURCE2?view=true.

Council of Science Editors:

Khoo PS. Molecular analysis of insulin action using high throughput genetic screens. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51670 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10337/SOURCE2?view=true


University of Michigan

5. Scharf, Nathan. Identification and Evaluation of Bacterial RNA Polymerase Inhibitors Using a Novel Plasmid-based Transcription Assay.

Degree: PhD, Medicinal Chemistry, 2017, University of Michigan

 Tuberculosis (TB) is a global health problem caused by Mycobacterium tuberculosis with 8-10 million new cases each year according to the World Health Organization. The… (more)

Subjects/Keywords: RNA polymerase; transcription; drug discovery; rifampin; high-throughput screen; tuberculosis; Biological Chemistry; Science

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APA (6th Edition):

Scharf, N. (2017). Identification and Evaluation of Bacterial RNA Polymerase Inhibitors Using a Novel Plasmid-based Transcription Assay. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/140941

Chicago Manual of Style (16th Edition):

Scharf, Nathan. “Identification and Evaluation of Bacterial RNA Polymerase Inhibitors Using a Novel Plasmid-based Transcription Assay.” 2017. Doctoral Dissertation, University of Michigan. Accessed January 20, 2021. http://hdl.handle.net/2027.42/140941.

MLA Handbook (7th Edition):

Scharf, Nathan. “Identification and Evaluation of Bacterial RNA Polymerase Inhibitors Using a Novel Plasmid-based Transcription Assay.” 2017. Web. 20 Jan 2021.

Vancouver:

Scharf N. Identification and Evaluation of Bacterial RNA Polymerase Inhibitors Using a Novel Plasmid-based Transcription Assay. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/2027.42/140941.

Council of Science Editors:

Scharf N. Identification and Evaluation of Bacterial RNA Polymerase Inhibitors Using a Novel Plasmid-based Transcription Assay. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/140941


RMIT University

6. Yang, L. Study on herb-drug interactions.

Degree: 2009, RMIT University

 Herbal medicines, such as St John's wort, garlic, gingko, and ginseng, are commonly used complementary therapies. The human CYP enzymes are a superfamily which consists… (more)

Subjects/Keywords: Fields of Research; Herb-drug interactions; Cytochrome P450; High throughput screen; Pharmacophore; Docking; Crystal structure; IC50; Pharmacokinetic principles; Prediction

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APA (6th Edition):

Yang, L. (2009). Study on herb-drug interactions. (Thesis). RMIT University. Retrieved from http://researchbank.rmit.edu.au/view/rmit:13374

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):

Yang, L. “Study on herb-drug interactions.” 2009. Thesis, RMIT University. Accessed January 20, 2021. http://researchbank.rmit.edu.au/view/rmit:13374.

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

MLA Handbook (7th Edition):

Yang, L. “Study on herb-drug interactions.” 2009. Web. 20 Jan 2021.

Vancouver:

Yang L. Study on herb-drug interactions. [Internet] [Thesis]. RMIT University; 2009. [cited 2021 Jan 20]. Available from: http://researchbank.rmit.edu.au/view/rmit:13374.

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

Council of Science Editors:

Yang L. Study on herb-drug interactions. [Thesis]. RMIT University; 2009. Available from: http://researchbank.rmit.edu.au/view/rmit:13374

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


University of Toronto

7. Hui, Wing. Development of a Novel Pck-1: eGFP Reporter Zebrafish Line for the Discovery and Evaluation of Potential Anti-Diabetic Drugs.

Degree: 2013, University of Toronto

Overexpression of Phosphoenolpyruvate carboxykinase - cytosolic (PEPCK, encoded by Pck-1 gene) has been found to be associated with the prevalence of hyperglycemia in Type 2… (more)

Subjects/Keywords: Diabetes Mellitus; gluconeogenesis; PEPCK; Pck-1; zebrafish; drug discovery; transgenics; reporter line; high throughput screening; transposon; gene regulation; novel drugs; drug screen; microinjection; deletional analysis; physiology; 0719

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APA (6th Edition):

Hui, W. (2013). Development of a Novel Pck-1: eGFP Reporter Zebrafish Line for the Discovery and Evaluation of Potential Anti-Diabetic Drugs. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42881

Chicago Manual of Style (16th Edition):

Hui, Wing. “Development of a Novel Pck-1: eGFP Reporter Zebrafish Line for the Discovery and Evaluation of Potential Anti-Diabetic Drugs.” 2013. Masters Thesis, University of Toronto. Accessed January 20, 2021. http://hdl.handle.net/1807/42881.

MLA Handbook (7th Edition):

Hui, Wing. “Development of a Novel Pck-1: eGFP Reporter Zebrafish Line for the Discovery and Evaluation of Potential Anti-Diabetic Drugs.” 2013. Web. 20 Jan 2021.

Vancouver:

Hui W. Development of a Novel Pck-1: eGFP Reporter Zebrafish Line for the Discovery and Evaluation of Potential Anti-Diabetic Drugs. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1807/42881.

Council of Science Editors:

Hui W. Development of a Novel Pck-1: eGFP Reporter Zebrafish Line for the Discovery and Evaluation of Potential Anti-Diabetic Drugs. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42881


University of Melbourne

8. Yan, Shunfei. A Genome-wide RNAi screen identifies combinatorial efficacy of CX-5461 with homologous recombination deficiency and Topoisomerase I inhibition in ovarian cancer.

Degree: 2019, University of Melbourne

High-grade serous ovarian cancer (HGSC) is common, with poor prognosis. Limited therapeutic options are available, and the development of new therapies is of high priority.… (more)

Subjects/Keywords: CX-5461; RNA polymerase I; Topoisomerase I; BRCA2; high-throughput screen; synergistic effects; drug combination; high-grade serous ovarian cancer; homologous recombination; DNA damage response

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APA (6th Edition):

Yan, S. (2019). A Genome-wide RNAi screen identifies combinatorial efficacy of CX-5461 with homologous recombination deficiency and Topoisomerase I inhibition in ovarian cancer. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/228850

Chicago Manual of Style (16th Edition):

Yan, Shunfei. “A Genome-wide RNAi screen identifies combinatorial efficacy of CX-5461 with homologous recombination deficiency and Topoisomerase I inhibition in ovarian cancer.” 2019. Doctoral Dissertation, University of Melbourne. Accessed January 20, 2021. http://hdl.handle.net/11343/228850.

MLA Handbook (7th Edition):

Yan, Shunfei. “A Genome-wide RNAi screen identifies combinatorial efficacy of CX-5461 with homologous recombination deficiency and Topoisomerase I inhibition in ovarian cancer.” 2019. Web. 20 Jan 2021.

Vancouver:

Yan S. A Genome-wide RNAi screen identifies combinatorial efficacy of CX-5461 with homologous recombination deficiency and Topoisomerase I inhibition in ovarian cancer. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/11343/228850.

Council of Science Editors:

Yan S. A Genome-wide RNAi screen identifies combinatorial efficacy of CX-5461 with homologous recombination deficiency and Topoisomerase I inhibition in ovarian cancer. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/228850


Georgia Tech

9. Orwig, Susan D. Biophysical and structural characterization of proteins implicated in glaucoma and Gaucher disease.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 The inherited form of primary open angle glaucoma, a disorder characterized by increased intraocular pressure and retina degeneration, is linked to mutations in the olfactomedin… (more)

Subjects/Keywords: Open-angle glaucoma; Pharmacological chaperones; High-throughput drug screen; Amyloid fibrils; Gaucher disease; Myocilin; Glaucoma; Eye Diseases; Eye Diseases Genetic aspects; Intraocular pressure; Body fluids Pressure; Eye

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APA (6th Edition):

Orwig, S. D. (2011). Biophysical and structural characterization of proteins implicated in glaucoma and Gaucher disease. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45816

Chicago Manual of Style (16th Edition):

Orwig, Susan D. “Biophysical and structural characterization of proteins implicated in glaucoma and Gaucher disease.” 2011. Doctoral Dissertation, Georgia Tech. Accessed January 20, 2021. http://hdl.handle.net/1853/45816.

MLA Handbook (7th Edition):

Orwig, Susan D. “Biophysical and structural characterization of proteins implicated in glaucoma and Gaucher disease.” 2011. Web. 20 Jan 2021.

Vancouver:

Orwig SD. Biophysical and structural characterization of proteins implicated in glaucoma and Gaucher disease. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1853/45816.

Council of Science Editors:

Orwig SD. Biophysical and structural characterization of proteins implicated in glaucoma and Gaucher disease. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/45816


Harvard University

10. Matano, Leigh M. Accelerating the Discovery of Antibacterial Compounds to Validate Drug Targets and Probe Cell Physiology of S. Aureus.

Degree: PhD, 2017, Harvard University

Methicillin-resistant Staphylococcus aureus (MRSA) is a Gram-positive pathogen identified by its resistance to beta-lactam antibiotics. In an era where drug-resistant infections are becoming harder and… (more)

Subjects/Keywords: Antibiotics; drug discovery; high-throughput screening

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APA (6th Edition):

Matano, L. M. (2017). Accelerating the Discovery of Antibacterial Compounds to Validate Drug Targets and Probe Cell Physiology of S. Aureus. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061471

Chicago Manual of Style (16th Edition):

Matano, Leigh M. “Accelerating the Discovery of Antibacterial Compounds to Validate Drug Targets and Probe Cell Physiology of S. Aureus.” 2017. Doctoral Dissertation, Harvard University. Accessed January 20, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061471.

MLA Handbook (7th Edition):

Matano, Leigh M. “Accelerating the Discovery of Antibacterial Compounds to Validate Drug Targets and Probe Cell Physiology of S. Aureus.” 2017. Web. 20 Jan 2021.

Vancouver:

Matano LM. Accelerating the Discovery of Antibacterial Compounds to Validate Drug Targets and Probe Cell Physiology of S. Aureus. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2021 Jan 20]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061471.

Council of Science Editors:

Matano LM. Accelerating the Discovery of Antibacterial Compounds to Validate Drug Targets and Probe Cell Physiology of S. Aureus. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061471


Oregon State University

11. Mandrell, David. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials.

Degree: MS, Industrial Engineering, 2010, Oregon State University

 The field of nanotechnology has been rapidly developing new materials. These materials have become incorporated into consumer products and the environment after only minimal assessment… (more)

Subjects/Keywords: Automation; High throughput screening (Drug development)

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APA (6th Edition):

Mandrell, D. (2010). Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/16495

Chicago Manual of Style (16th Edition):

Mandrell, David. “Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials.” 2010. Masters Thesis, Oregon State University. Accessed January 20, 2021. http://hdl.handle.net/1957/16495.

MLA Handbook (7th Edition):

Mandrell, David. “Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials.” 2010. Web. 20 Jan 2021.

Vancouver:

Mandrell D. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. [Internet] [Masters thesis]. Oregon State University; 2010. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1957/16495.

Council of Science Editors:

Mandrell D. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. [Masters Thesis]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/16495

12. Ent, Wietske van der. In vivo modelling of Ewing sarcoma in zebrafish.

Degree: 2015, Faculty of Science, Leiden University

 Ewing sarcoma (EWS) is a disease with a high need for novel therapeutic strategies. To aid in investigating such compounds in an in vivo setting,… (more)

Subjects/Keywords: Zebrafish; Transgenic animal model; Xenograft model; Anti-cancer drug screen; High-throughput; Zebrafish; Transgenic animal model; Xenograft model; Anti-cancer drug screen; High-throughput

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APA (6th Edition):

Ent, W. v. d. (2015). In vivo modelling of Ewing sarcoma in zebrafish. (Doctoral Dissertation). Faculty of Science, Leiden University. Retrieved from http://hdl.handle.net/1887/35942

Chicago Manual of Style (16th Edition):

Ent, Wietske van der. “In vivo modelling of Ewing sarcoma in zebrafish.” 2015. Doctoral Dissertation, Faculty of Science, Leiden University. Accessed January 20, 2021. http://hdl.handle.net/1887/35942.

MLA Handbook (7th Edition):

Ent, Wietske van der. “In vivo modelling of Ewing sarcoma in zebrafish.” 2015. Web. 20 Jan 2021.

Vancouver:

Ent Wvd. In vivo modelling of Ewing sarcoma in zebrafish. [Internet] [Doctoral dissertation]. Faculty of Science, Leiden University; 2015. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1887/35942.

Council of Science Editors:

Ent Wvd. In vivo modelling of Ewing sarcoma in zebrafish. [Doctoral Dissertation]. Faculty of Science, Leiden University; 2015. Available from: http://hdl.handle.net/1887/35942


UCLA

13. 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 January 20, 2021. 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. 20 Jan 2021.

Vancouver:

Douglas CJ. Investigation and Characterization of Small Molecule Modulators for Mitochondrial Processing Peptidase. [Internet] [Thesis]. UCLA; 2014. [cited 2021 Jan 20]. 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 Ottawa

14. Allan, Kristina Jean. Enhancing Oncolytic Virotherapy Using Functional Genomic Screening .

Degree: 2018, University of Ottawa

At the author’s request, the abstract has been removed due to the confidential nature of the thesis. It will be added once the embargo period has passed.

Subjects/Keywords: oncolytic; virotherapy; cancer; RNAi; vaccinia; screen; high-throughput

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APA (6th Edition):

Allan, K. J. (2018). Enhancing Oncolytic Virotherapy Using Functional Genomic Screening . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37910

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):

Allan, Kristina Jean. “Enhancing Oncolytic Virotherapy Using Functional Genomic Screening .” 2018. Thesis, University of Ottawa. Accessed January 20, 2021. http://hdl.handle.net/10393/37910.

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

MLA Handbook (7th Edition):

Allan, Kristina Jean. “Enhancing Oncolytic Virotherapy Using Functional Genomic Screening .” 2018. Web. 20 Jan 2021.

Vancouver:

Allan KJ. Enhancing Oncolytic Virotherapy Using Functional Genomic Screening . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10393/37910.

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

Council of Science Editors:

Allan KJ. Enhancing Oncolytic Virotherapy Using Functional Genomic Screening . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37910

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


Wayne State University

15. Colangelo, Wesley David. In vivo display: a selection and its derivatives for antimicrobial peptide lead identification.

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

  The rise of antibiotic resistance necessitates new approaches for the isolation of new antimicrobials with novel inhibitory mechanisms, bypassing the development of rapid resistance… (more)

Subjects/Keywords: Antimicrobial, High-throughput, Peptide, Screen; Microbiology; Molecular Biology

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APA (6th Edition):

Colangelo, W. D. (2012). In vivo display: a selection and its derivatives for antimicrobial peptide lead identification. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/501

Chicago Manual of Style (16th Edition):

Colangelo, Wesley David. “In vivo display: a selection and its derivatives for antimicrobial peptide lead identification.” 2012. Doctoral Dissertation, Wayne State University. Accessed January 20, 2021. https://digitalcommons.wayne.edu/oa_dissertations/501.

MLA Handbook (7th Edition):

Colangelo, Wesley David. “In vivo display: a selection and its derivatives for antimicrobial peptide lead identification.” 2012. Web. 20 Jan 2021.

Vancouver:

Colangelo WD. In vivo display: a selection and its derivatives for antimicrobial peptide lead identification. [Internet] [Doctoral dissertation]. Wayne State University; 2012. [cited 2021 Jan 20]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/501.

Council of Science Editors:

Colangelo WD. In vivo display: a selection and its derivatives for antimicrobial peptide lead identification. [Doctoral Dissertation]. Wayne State University; 2012. Available from: https://digitalcommons.wayne.edu/oa_dissertations/501


University of California – San Diego

16. Li, Zheng. A Localized Pseudomonas syringae Infection Triggers Systemic Clock Responses in Arabidopsis.

Degree: Biology, 2018, University of California – San Diego

 Many plant physiological and behavioral responses exhibit 24h rhythms that anticipate daily changes in the environment. This key adaptive response is regulated by the circadian… (more)

Subjects/Keywords: Biology; Circadian clock; high throughput yeast screen; Pseudomonas syringae; TCP

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APA (6th Edition):

Li, Z. (2018). A Localized Pseudomonas syringae Infection Triggers Systemic Clock Responses in Arabidopsis. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/4880d2dq

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):

Li, Zheng. “A Localized Pseudomonas syringae Infection Triggers Systemic Clock Responses in Arabidopsis.” 2018. Thesis, University of California – San Diego. Accessed January 20, 2021. http://www.escholarship.org/uc/item/4880d2dq.

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

MLA Handbook (7th Edition):

Li, Zheng. “A Localized Pseudomonas syringae Infection Triggers Systemic Clock Responses in Arabidopsis.” 2018. Web. 20 Jan 2021.

Vancouver:

Li Z. A Localized Pseudomonas syringae Infection Triggers Systemic Clock Responses in Arabidopsis. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2021 Jan 20]. Available from: http://www.escholarship.org/uc/item/4880d2dq.

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

Council of Science Editors:

Li Z. A Localized Pseudomonas syringae Infection Triggers Systemic Clock Responses in Arabidopsis. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/4880d2dq

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


Boston College

17. Ceyhan, Ozge. Identification of biologically-active PDE11-selective inhibitors using a yeast-based high throughput screen.

Degree: PhD, Biology, 2012, Boston College

 The biological roles of the most recently discovered mammalian cyclic nucleotide phosphodiesterase (PDE) family, PDE11, are poorly understood, in part due to the lack of… (more)

Subjects/Keywords: adrenal hyperplasia; Cushing syndrome; high throughput screen; inhibitor; PDE11; Phosphodiesterases

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APA (6th Edition):

Ceyhan, O. (2012). Identification of biologically-active PDE11-selective inhibitors using a yeast-based high throughput screen. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101539

Chicago Manual of Style (16th Edition):

Ceyhan, Ozge. “Identification of biologically-active PDE11-selective inhibitors using a yeast-based high throughput screen.” 2012. Doctoral Dissertation, Boston College. Accessed January 20, 2021. http://dlib.bc.edu/islandora/object/bc-ir:101539.

MLA Handbook (7th Edition):

Ceyhan, Ozge. “Identification of biologically-active PDE11-selective inhibitors using a yeast-based high throughput screen.” 2012. Web. 20 Jan 2021.

Vancouver:

Ceyhan O. Identification of biologically-active PDE11-selective inhibitors using a yeast-based high throughput screen. [Internet] [Doctoral dissertation]. Boston College; 2012. [cited 2021 Jan 20]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101539.

Council of Science Editors:

Ceyhan O. Identification of biologically-active PDE11-selective inhibitors using a yeast-based high throughput screen. [Doctoral Dissertation]. Boston College; 2012. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101539


University of Ottawa

18. Elnour, Nada. Reporter-based Synthetic Genetic Analysis of Budding Yeast Reveals Novel MMS-induced Effectors of the RNR3 Promoter .

Degree: 2016, University of Ottawa

 The DNA damage response is a cell-wide response that coordinates repair and cell-cycle progression. Crucial to fidelity of genetic propagation, survival, and apoptosis, dysfunctions in… (more)

Subjects/Keywords: Reporter synthetic genetic array; Flow cytometry; RNR3 promoter; DNA damage response; High-throughput screen; Methyl methanesulfonate; Differential EMAP; Chemogenetic screen

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APA (6th Edition):

Elnour, N. (2016). Reporter-based Synthetic Genetic Analysis of Budding Yeast Reveals Novel MMS-induced Effectors of the RNR3 Promoter . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35143

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):

Elnour, Nada. “Reporter-based Synthetic Genetic Analysis of Budding Yeast Reveals Novel MMS-induced Effectors of the RNR3 Promoter .” 2016. Thesis, University of Ottawa. Accessed January 20, 2021. http://hdl.handle.net/10393/35143.

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

MLA Handbook (7th Edition):

Elnour, Nada. “Reporter-based Synthetic Genetic Analysis of Budding Yeast Reveals Novel MMS-induced Effectors of the RNR3 Promoter .” 2016. Web. 20 Jan 2021.

Vancouver:

Elnour N. Reporter-based Synthetic Genetic Analysis of Budding Yeast Reveals Novel MMS-induced Effectors of the RNR3 Promoter . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10393/35143.

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

Council of Science Editors:

Elnour N. Reporter-based Synthetic Genetic Analysis of Budding Yeast Reveals Novel MMS-induced Effectors of the RNR3 Promoter . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35143

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


University of California – Berkeley

19. Visperas, Patrick Ramos. Inhibition of the T-cell Kinase ZAP-70.

Degree: Molecular & Cell Biology, 2013, University of California – Berkeley

 The adaptive immune system responds to foreign antigens to produce a highly specific immune response. T-cells, a type of white blood cell of the adaptive… (more)

Subjects/Keywords: Biophysics; Biochemistry; Adaptive Immune System; High throughput screen; Inhibitor; Kinase; T-cell; ZAP-70

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APA (6th Edition):

Visperas, P. R. (2013). Inhibition of the T-cell Kinase ZAP-70. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/16j1b7gb

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):

Visperas, Patrick Ramos. “Inhibition of the T-cell Kinase ZAP-70.” 2013. Thesis, University of California – Berkeley. Accessed January 20, 2021. http://www.escholarship.org/uc/item/16j1b7gb.

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

MLA Handbook (7th Edition):

Visperas, Patrick Ramos. “Inhibition of the T-cell Kinase ZAP-70.” 2013. Web. 20 Jan 2021.

Vancouver:

Visperas PR. Inhibition of the T-cell Kinase ZAP-70. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2021 Jan 20]. Available from: http://www.escholarship.org/uc/item/16j1b7gb.

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

Council of Science Editors:

Visperas PR. Inhibition of the T-cell Kinase ZAP-70. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/16j1b7gb

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


Vanderbilt University

20. Ashbrook, Alison Whitney. Unveiling Strategies for Chikungunya Virus Attenuation and Antiviral Therapy.

Degree: PhD, Microbiology and Immunology, 2015, Vanderbilt University

 Chikungunya virus (CHIKV) is a mosquito-borne cause of epidemics of debilitating arthritis worldwide. Currently, there are no licensed vaccines or antiviral therapies available for the… (more)

Subjects/Keywords: sodium-potassium ATPase; digoxin; attachment; glycosaminoglycan; high-throughput screen; immunoproteasome; PSME2; arthritis; alphavirus; chikungunya virus

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APA (6th Edition):

Ashbrook, A. W. (2015). Unveiling Strategies for Chikungunya Virus Attenuation and Antiviral Therapy. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13092

Chicago Manual of Style (16th Edition):

Ashbrook, Alison Whitney. “Unveiling Strategies for Chikungunya Virus Attenuation and Antiviral Therapy.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed January 20, 2021. http://hdl.handle.net/1803/13092.

MLA Handbook (7th Edition):

Ashbrook, Alison Whitney. “Unveiling Strategies for Chikungunya Virus Attenuation and Antiviral Therapy.” 2015. Web. 20 Jan 2021.

Vancouver:

Ashbrook AW. Unveiling Strategies for Chikungunya Virus Attenuation and Antiviral Therapy. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1803/13092.

Council of Science Editors:

Ashbrook AW. Unveiling Strategies for Chikungunya Virus Attenuation and Antiviral Therapy. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/13092


Freie Universität Berlin

21. Hoffmann, Hans-Heinrich. Identifizierung neuartiger Wirkstoffe zur Inhibierung oder Verstärkung der Replikation des Influenza Virus mittels eines High-throughput Screens kleinmolekularer Verbindungen.

Degree: 2011, Freie Universität Berlin

 Die Zahl schwerer Atemwegserkrankungen hervorgerufen durch das Influenza Virus liegt jaehrlich bei 3-5 Millionen and verursacht bis zu 500,000 Todesfaelle weltweit. Der Ausbruch und die… (more)

Subjects/Keywords: antiviral; high-throughput screen; influenza virus; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie

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APA (6th Edition):

Hoffmann, H. (2011). Identifizierung neuartiger Wirkstoffe zur Inhibierung oder Verstärkung der Replikation des Influenza Virus mittels eines High-throughput Screens kleinmolekularer Verbindungen. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-11211

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):

Hoffmann, Hans-Heinrich. “Identifizierung neuartiger Wirkstoffe zur Inhibierung oder Verstärkung der Replikation des Influenza Virus mittels eines High-throughput Screens kleinmolekularer Verbindungen.” 2011. Thesis, Freie Universität Berlin. Accessed January 20, 2021. http://dx.doi.org/10.17169/refubium-11211.

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

MLA Handbook (7th Edition):

Hoffmann, Hans-Heinrich. “Identifizierung neuartiger Wirkstoffe zur Inhibierung oder Verstärkung der Replikation des Influenza Virus mittels eines High-throughput Screens kleinmolekularer Verbindungen.” 2011. Web. 20 Jan 2021.

Vancouver:

Hoffmann H. Identifizierung neuartiger Wirkstoffe zur Inhibierung oder Verstärkung der Replikation des Influenza Virus mittels eines High-throughput Screens kleinmolekularer Verbindungen. [Internet] [Thesis]. Freie Universität Berlin; 2011. [cited 2021 Jan 20]. Available from: http://dx.doi.org/10.17169/refubium-11211.

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

Council of Science Editors:

Hoffmann H. Identifizierung neuartiger Wirkstoffe zur Inhibierung oder Verstärkung der Replikation des Influenza Virus mittels eines High-throughput Screens kleinmolekularer Verbindungen. [Thesis]. Freie Universität Berlin; 2011. Available from: http://dx.doi.org/10.17169/refubium-11211

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


University of New Mexico

22. Sully, Erin. Small molecule inhibition of Staphylococcus aureus virulence.

Degree: Biomedical Sciences Graduate Program, 2011, University of New Mexico

 The increasing emergence of antibiotic resistant Staphylococcus aureus infections, particularly those caused by a single clone of methicillin resistant S. aureus (USA300 MRSA), coupled with… (more)

Subjects/Keywords: CA-MRSA; staphylococcus aureus; small molecule inhibitor; high-throughput screen; virulence; quorum sensing

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APA (6th Edition):

Sully, E. (2011). Small molecule inhibition of Staphylococcus aureus virulence. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/39

Chicago Manual of Style (16th Edition):

Sully, Erin. “Small molecule inhibition of Staphylococcus aureus virulence.” 2011. Doctoral Dissertation, University of New Mexico. Accessed January 20, 2021. https://digitalrepository.unm.edu/biom_etds/39.

MLA Handbook (7th Edition):

Sully, Erin. “Small molecule inhibition of Staphylococcus aureus virulence.” 2011. Web. 20 Jan 2021.

Vancouver:

Sully E. Small molecule inhibition of Staphylococcus aureus virulence. [Internet] [Doctoral dissertation]. University of New Mexico; 2011. [cited 2021 Jan 20]. Available from: https://digitalrepository.unm.edu/biom_etds/39.

Council of Science Editors:

Sully E. Small molecule inhibition of Staphylococcus aureus virulence. [Doctoral Dissertation]. University of New Mexico; 2011. Available from: https://digitalrepository.unm.edu/biom_etds/39


University of Melbourne

23. Moore, Darcy. Identification of epigenetic modifiers involved in neural stem cell function.

Degree: 2015, University of Melbourne

 It has become clear that epigenetic modifications of chromatin play a crucial role in regulating gene expression and cell fate decisions in stem cells; however,… (more)

Subjects/Keywords: epigenetics; neural stem cell; Yy1; Prdm8; RNAi; high throughput screen; brain cancer

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APA (6th Edition):

Moore, D. (2015). Identification of epigenetic modifiers involved in neural stem cell function. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/55768

Chicago Manual of Style (16th Edition):

Moore, Darcy. “Identification of epigenetic modifiers involved in neural stem cell function.” 2015. Doctoral Dissertation, University of Melbourne. Accessed January 20, 2021. http://hdl.handle.net/11343/55768.

MLA Handbook (7th Edition):

Moore, Darcy. “Identification of epigenetic modifiers involved in neural stem cell function.” 2015. Web. 20 Jan 2021.

Vancouver:

Moore D. Identification of epigenetic modifiers involved in neural stem cell function. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/11343/55768.

Council of Science Editors:

Moore D. Identification of epigenetic modifiers involved in neural stem cell function. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/55768


University of Edinburgh

24. Spitzer, Michaela. Chemical-genetic interrogation of small molecule mechanism of action in S. cerevisiae.

Degree: PhD, 2011, University of Edinburgh

 The budding yeast S. cerevisiae is widely used as a model organism to study biological processes that are conserved among eukaryotes. Di fferent genomic approaches… (more)

Subjects/Keywords: 615.1; chemical biology; S. cerevisiae; small molecules; high-throughput screen; chemical genetics

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APA (6th Edition):

Spitzer, M. (2011). Chemical-genetic interrogation of small molecule mechanism of action in S. cerevisiae. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5733

Chicago Manual of Style (16th Edition):

Spitzer, Michaela. “Chemical-genetic interrogation of small molecule mechanism of action in S. cerevisiae.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed January 20, 2021. http://hdl.handle.net/1842/5733.

MLA Handbook (7th Edition):

Spitzer, Michaela. “Chemical-genetic interrogation of small molecule mechanism of action in S. cerevisiae.” 2011. Web. 20 Jan 2021.

Vancouver:

Spitzer M. Chemical-genetic interrogation of small molecule mechanism of action in S. cerevisiae. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1842/5733.

Council of Science Editors:

Spitzer M. Chemical-genetic interrogation of small molecule mechanism of action in S. cerevisiae. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5733


University of Maryland

25. Yuan, Xiaojing. FUNCTIONAL INSIGHTS INTO HRG-1-MEDIATED HEME TRANSPORT.

Degree: Animal Sciences, 2012, University of Maryland

 Heme is an essential cofactor involved in various biological processes including oxygen transport, xenobiotic detoxification, oxidative metabolism, gas sensing, circadian rhythm, signal transduction, microRNA processing… (more)

Subjects/Keywords: Molecular biology; Genetics; Parasitology; heme; high-throughput screen; iron; parasite; transport; yeast

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APA (6th Edition):

Yuan, X. (2012). FUNCTIONAL INSIGHTS INTO HRG-1-MEDIATED HEME TRANSPORT. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/13522

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):

Yuan, Xiaojing. “FUNCTIONAL INSIGHTS INTO HRG-1-MEDIATED HEME TRANSPORT.” 2012. Thesis, University of Maryland. Accessed January 20, 2021. http://hdl.handle.net/1903/13522.

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

MLA Handbook (7th Edition):

Yuan, Xiaojing. “FUNCTIONAL INSIGHTS INTO HRG-1-MEDIATED HEME TRANSPORT.” 2012. Web. 20 Jan 2021.

Vancouver:

Yuan X. FUNCTIONAL INSIGHTS INTO HRG-1-MEDIATED HEME TRANSPORT. [Internet] [Thesis]. University of Maryland; 2012. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1903/13522.

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

Council of Science Editors:

Yuan X. FUNCTIONAL INSIGHTS INTO HRG-1-MEDIATED HEME TRANSPORT. [Thesis]. University of Maryland; 2012. Available from: http://hdl.handle.net/1903/13522

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


University of Georgia

26. Kukday, Sayali Shrikant. Modulating insulin-degrading enzyme activity.

Degree: 2014, University of Georgia

 The insulin-degrading enzyme (IDE), a Zn2+-dependent metalloprotease, degrades several physiologically important peptides including Aβ, a peptide involved in the pathogenesis of Alzheimer’s disease. Enhancing IDE… (more)

Subjects/Keywords: Alzheimer’s disease; ; insulin-degrading enzyme; activator; protease; high-throughput screen; fluorescence; yeast; a-factor

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APA (6th Edition):

Kukday, S. S. (2014). Modulating insulin-degrading enzyme activity. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/28313

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):

Kukday, Sayali Shrikant. “Modulating insulin-degrading enzyme activity.” 2014. Thesis, University of Georgia. Accessed January 20, 2021. http://hdl.handle.net/10724/28313.

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

MLA Handbook (7th Edition):

Kukday, Sayali Shrikant. “Modulating insulin-degrading enzyme activity.” 2014. Web. 20 Jan 2021.

Vancouver:

Kukday SS. Modulating insulin-degrading enzyme activity. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10724/28313.

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

Council of Science Editors:

Kukday SS. Modulating insulin-degrading enzyme activity. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/28313

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

27. Lapin, Valentina. RNAi Screening of the Kinome to Identify Mediators of proliferation and trastuzumab (Herceptin) resistance in HER2 Breast Cancers.

Degree: 2012, University of Toronto

Breast cancers with overexpression or amplification of the HER2 tyrosine kinase receptor are more aggressive, resistant to chemotherapy, and associated with a worse prognosis. Currently,… (more)

Subjects/Keywords: RNAi; HER2; high-throughput screen; breast cancer; trastuzumab; Herceptin; drug resistance; siRNA; 0992; 0307; 0369

…75 2.5.1 Experimental variability in high-­‐throughput screening… …47 2.3.4 Screen data normalization… …cancer cell lines .............. 63 2.4.6 Sensitizer screen… …95 3 SIRNA KINOME SCREEN OF HER2+ BREAST CANCER CELL LINES… …110 3.3.7 Drug treatments… 

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APA (6th Edition):

Lapin, V. (2012). RNAi Screening of the Kinome to Identify Mediators of proliferation and trastuzumab (Herceptin) resistance in HER2 Breast Cancers. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/35712

Chicago Manual of Style (16th Edition):

Lapin, Valentina. “RNAi Screening of the Kinome to Identify Mediators of proliferation and trastuzumab (Herceptin) resistance in HER2 Breast Cancers.” 2012. Doctoral Dissertation, University of Toronto. Accessed January 20, 2021. http://hdl.handle.net/1807/35712.

MLA Handbook (7th Edition):

Lapin, Valentina. “RNAi Screening of the Kinome to Identify Mediators of proliferation and trastuzumab (Herceptin) resistance in HER2 Breast Cancers.” 2012. Web. 20 Jan 2021.

Vancouver:

Lapin V. RNAi Screening of the Kinome to Identify Mediators of proliferation and trastuzumab (Herceptin) resistance in HER2 Breast Cancers. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1807/35712.

Council of Science Editors:

Lapin V. RNAi Screening of the Kinome to Identify Mediators of proliferation and trastuzumab (Herceptin) resistance in HER2 Breast Cancers. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/35712


University of California – Santa Cruz

28. Woehrmann, Marcos H. Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms.

Degree: Biomolecular Engineering and Bioinformatics, 2015, University of California – Santa Cruz

 To develop more effective therapies to treat human diseases, a better method of finding the biological targets and modes of action of new compounds is… (more)

Subjects/Keywords: Bioinformatics; Bioinformatics; Cytological Profiling; Drug Target Prediction; High-throughput Screening; HTS

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APA (6th Edition):

Woehrmann, M. H. (2015). Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/9976p4ch

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):

Woehrmann, Marcos H. “Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms.” 2015. Thesis, University of California – Santa Cruz. Accessed January 20, 2021. http://www.escholarship.org/uc/item/9976p4ch.

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

MLA Handbook (7th Edition):

Woehrmann, Marcos H. “Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms.” 2015. Web. 20 Jan 2021.

Vancouver:

Woehrmann MH. Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms. [Internet] [Thesis]. University of California – Santa Cruz; 2015. [cited 2021 Jan 20]. Available from: http://www.escholarship.org/uc/item/9976p4ch.

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

Council of Science Editors:

Woehrmann MH. Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms. [Thesis]. University of California – Santa Cruz; 2015. Available from: http://www.escholarship.org/uc/item/9976p4ch

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


Texas A&M University

29. LaiHing, Steven 1983-. Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis.

Degree: MS, Biochemistry, 2011, Texas A&M University

 Mycobacterium tuberculosis currently affects 1/3 of the world's population. Over the past 20 years tuberculosis has become more resistant to all front line drugs used… (more)

Subjects/Keywords: HTS; TB; MTB; Drug Development and Design; High Throughput Screening; Tuberculosis

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APA (6th Edition):

LaiHing, S. 1. (2011). Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153195

Chicago Manual of Style (16th Edition):

LaiHing, Steven 1983-. “Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis.” 2011. Masters Thesis, Texas A&M University. Accessed January 20, 2021. http://hdl.handle.net/1969.1/153195.

MLA Handbook (7th Edition):

LaiHing, Steven 1983-. “Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis.” 2011. Web. 20 Jan 2021.

Vancouver:

LaiHing S1. Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis. [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1969.1/153195.

Council of Science Editors:

LaiHing S1. Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis. [Masters Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/153195


Columbia University

30. Yozwiak, Carrie Elizabeth. Development of Methods for the Discovery of Small Molecule Biological Probes.

Degree: 2017, Columbia University

 Advances in combinatorial chemistry have facilitated the production of large chemical libraries that can be used as tools to discover biological probes and therapeutics. High-throughput(more)

Subjects/Keywords: Chemistry; Biology; Molecular probes; High throughput screening (Drug development)

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

APA (6th Edition):

Yozwiak, C. E. (2017). Development of Methods for the Discovery of Small Molecule Biological Probes. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8NZ8KW9

Chicago Manual of Style (16th Edition):

Yozwiak, Carrie Elizabeth. “Development of Methods for the Discovery of Small Molecule Biological Probes.” 2017. Doctoral Dissertation, Columbia University. Accessed January 20, 2021. https://doi.org/10.7916/D8NZ8KW9.

MLA Handbook (7th Edition):

Yozwiak, Carrie Elizabeth. “Development of Methods for the Discovery of Small Molecule Biological Probes.” 2017. Web. 20 Jan 2021.

Vancouver:

Yozwiak CE. Development of Methods for the Discovery of Small Molecule Biological Probes. [Internet] [Doctoral dissertation]. Columbia University; 2017. [cited 2021 Jan 20]. Available from: https://doi.org/10.7916/D8NZ8KW9.

Council of Science Editors:

Yozwiak CE. Development of Methods for the Discovery of Small Molecule Biological Probes. [Doctoral Dissertation]. Columbia University; 2017. Available from: https://doi.org/10.7916/D8NZ8KW9

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