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You searched for subject:(drug screening). Showing records 1 – 30 of 312 total matches.

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University of Illinois – Urbana-Champaign

1. Lidstone, Erich A. Identifying small molecule aggregators with photonic crystal biosensor microplates.

Degree: MS, 0408, 2011, University of Illinois – Urbana-Champaign

 Small molecules identified through high-throughput screens are essential elements in pharmaceutical discovery programs. It is now recognized that a substantial fraction of small molecules exhibit… (more)

Subjects/Keywords: Biosensors; Photonic crystals; pharmaceutical screening; small molecule screening; drug screening

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

APA (6th Edition):

Lidstone, E. A. (2011). Identifying small molecule aggregators with photonic crystal biosensor microplates. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18539

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):

Lidstone, Erich A. “Identifying small molecule aggregators with photonic crystal biosensor microplates.” 2011. Thesis, University of Illinois – Urbana-Champaign. Accessed November 27, 2020. http://hdl.handle.net/2142/18539.

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

MLA Handbook (7th Edition):

Lidstone, Erich A. “Identifying small molecule aggregators with photonic crystal biosensor microplates.” 2011. Web. 27 Nov 2020.

Vancouver:

Lidstone EA. Identifying small molecule aggregators with photonic crystal biosensor microplates. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2142/18539.

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

Council of Science Editors:

Lidstone EA. Identifying small molecule aggregators with photonic crystal biosensor microplates. [Thesis]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18539

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


Vanderbilt University

2. Kaufmann, Kristian Wallace. Computational prediction of protein small molecule interfaces using ROSETTA.

Degree: PhD, Chemistry, 2011, Vanderbilt University

 Protein small molecule docking has focused on the modeling of small molecule flexibility and scoring of small molecules binding to fixed protein structures due to… (more)

Subjects/Keywords: homology modeling; virtual screening; drug design

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APA (6th Edition):

Kaufmann, K. W. (2011). Computational prediction of protein small molecule interfaces using ROSETTA. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14473

Chicago Manual of Style (16th Edition):

Kaufmann, Kristian Wallace. “Computational prediction of protein small molecule interfaces using ROSETTA.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed November 27, 2020. http://hdl.handle.net/1803/14473.

MLA Handbook (7th Edition):

Kaufmann, Kristian Wallace. “Computational prediction of protein small molecule interfaces using ROSETTA.” 2011. Web. 27 Nov 2020.

Vancouver:

Kaufmann KW. Computational prediction of protein small molecule interfaces using ROSETTA. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1803/14473.

Council of Science Editors:

Kaufmann KW. Computational prediction of protein small molecule interfaces using ROSETTA. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/14473


Victoria University of Wellington

3. Yibmantasiri, Ploi. Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae.

Degree: 2012, Victoria University of Wellington

 One of the major problems in biology is to identify genes that are involved in specific processes. Classical genetics and biochemistry, although powerful and informative,… (more)

Subjects/Keywords: Genome-wide screening; Genetic networks; Drug resistance

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APA (6th Edition):

Yibmantasiri, P. (2012). Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2539

Chicago Manual of Style (16th Edition):

Yibmantasiri, Ploi. “Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae.” 2012. Doctoral Dissertation, Victoria University of Wellington. Accessed November 27, 2020. http://hdl.handle.net/10063/2539.

MLA Handbook (7th Edition):

Yibmantasiri, Ploi. “Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae.” 2012. Web. 27 Nov 2020.

Vancouver:

Yibmantasiri P. Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10063/2539.

Council of Science Editors:

Yibmantasiri P. Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae. [Doctoral Dissertation]. Victoria University of Wellington; 2012. Available from: http://hdl.handle.net/10063/2539


Harvard University

4. 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 November 27, 2020. 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. 27 Nov 2020.

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 2020 Nov 27]. 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


University of Toronto

5. Shen, Trong. Micropatterning of Novel Deformable Culture Substrates for Enhanced Contraction Force Measurements of Heart Muscle Cells in Drug Screening Application.

Degree: 2019, University of Toronto

Drugs excelled in preclinical assessment fail in clinical trials due to cardiovascular side effects. Human induced pluripotent stem-cell (iPSC)-derived cardiomyocytes (CMs) are used as sentinels… (more)

Subjects/Keywords: Cardiomyocytes; Drug Screening; Force Measurements; Micropatterning; 0202

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APA (6th Edition):

Shen, T. (2019). Micropatterning of Novel Deformable Culture Substrates for Enhanced Contraction Force Measurements of Heart Muscle Cells in Drug Screening Application. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/101817

Chicago Manual of Style (16th Edition):

Shen, Trong. “Micropatterning of Novel Deformable Culture Substrates for Enhanced Contraction Force Measurements of Heart Muscle Cells in Drug Screening Application.” 2019. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/101817.

MLA Handbook (7th Edition):

Shen, Trong. “Micropatterning of Novel Deformable Culture Substrates for Enhanced Contraction Force Measurements of Heart Muscle Cells in Drug Screening Application.” 2019. Web. 27 Nov 2020.

Vancouver:

Shen T. Micropatterning of Novel Deformable Culture Substrates for Enhanced Contraction Force Measurements of Heart Muscle Cells in Drug Screening Application. [Internet] [Masters thesis]. University of Toronto; 2019. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/101817.

Council of Science Editors:

Shen T. Micropatterning of Novel Deformable Culture Substrates for Enhanced Contraction Force Measurements of Heart Muscle Cells in Drug Screening Application. [Masters Thesis]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/101817


Oregon State University

6. 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 November 27, 2020. 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. 27 Nov 2020.

Vancouver:

Mandrell D. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. [Internet] [Masters thesis]. Oregon State University; 2010. [cited 2020 Nov 27]. 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


University of Oxford

7. Tso, Cynthia K. W. A reassessment of the interaction between complement C3d and complement receptor CD21 SCR1-2.

Degree: PhD, 2012, University of Oxford

 Biophysical characterisation of protein – ligand interactions can provide vital information to dissect complex biochemical binding mechanisms. C3d has been shown to interact with a… (more)

Subjects/Keywords: 572.696; Biochemistry; complement; C3d; crystallography; drug screening

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APA (6th Edition):

Tso, C. K. W. (2012). A reassessment of the interaction between complement C3d and complement receptor CD21 SCR1-2. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:29114281-a320-459d-88a6-9b5fad7c3f7f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572584

Chicago Manual of Style (16th Edition):

Tso, Cynthia K W. “A reassessment of the interaction between complement C3d and complement receptor CD21 SCR1-2.” 2012. Doctoral Dissertation, University of Oxford. Accessed November 27, 2020. http://ora.ox.ac.uk/objects/uuid:29114281-a320-459d-88a6-9b5fad7c3f7f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572584.

MLA Handbook (7th Edition):

Tso, Cynthia K W. “A reassessment of the interaction between complement C3d and complement receptor CD21 SCR1-2.” 2012. Web. 27 Nov 2020.

Vancouver:

Tso CKW. A reassessment of the interaction between complement C3d and complement receptor CD21 SCR1-2. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Nov 27]. Available from: http://ora.ox.ac.uk/objects/uuid:29114281-a320-459d-88a6-9b5fad7c3f7f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572584.

Council of Science Editors:

Tso CKW. A reassessment of the interaction between complement C3d and complement receptor CD21 SCR1-2. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:29114281-a320-459d-88a6-9b5fad7c3f7f ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.572584


University of Toronto

8. Rotin, Lianne Emily. Preclinical Evaluation of Synergistic Drug Combinations in Acute Myeloid Leukemia.

Degree: PhD, 2016, University of Toronto

 The FDA-approved Bruton’s tyrosine kinase (BTK) inhibitor ibrutinib has significantly improved patient outcomes in B-cell malignancies, where BTK signaling is implicated in disease progression. Documented… (more)

Subjects/Keywords: Acute myeloid leukemia; Drug screening; 0379

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APA (6th Edition):

Rotin, L. E. (2016). Preclinical Evaluation of Synergistic Drug Combinations in Acute Myeloid Leukemia. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/76804

Chicago Manual of Style (16th Edition):

Rotin, Lianne Emily. “Preclinical Evaluation of Synergistic Drug Combinations in Acute Myeloid Leukemia.” 2016. Doctoral Dissertation, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/76804.

MLA Handbook (7th Edition):

Rotin, Lianne Emily. “Preclinical Evaluation of Synergistic Drug Combinations in Acute Myeloid Leukemia.” 2016. Web. 27 Nov 2020.

Vancouver:

Rotin LE. Preclinical Evaluation of Synergistic Drug Combinations in Acute Myeloid Leukemia. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/76804.

Council of Science Editors:

Rotin LE. Preclinical Evaluation of Synergistic Drug Combinations in Acute Myeloid Leukemia. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76804


Virginia Tech

9. Elvington, Elizabeth Ashcraft Savage. Contactless Dielectrophoresis towards Drug Screening and Microdevice Development for Cell Sorting.

Degree: MS, Biomedical Engineering, 2013, Virginia Tech

 Firstly, this work demonstrates that contactless dielectrophoresis (cDEP) was useful to detect a reversal in the electrical phenotype of late-stage ovarian cancer cells to a… (more)

Subjects/Keywords: Dielectrophoresis; Drug screening; Cell sorting; Ovarian cancer

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APA (6th Edition):

Elvington, E. A. S. (2013). Contactless Dielectrophoresis towards Drug Screening and Microdevice Development for Cell Sorting. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/23294

Chicago Manual of Style (16th Edition):

Elvington, Elizabeth Ashcraft Savage. “Contactless Dielectrophoresis towards Drug Screening and Microdevice Development for Cell Sorting.” 2013. Masters Thesis, Virginia Tech. Accessed November 27, 2020. http://hdl.handle.net/10919/23294.

MLA Handbook (7th Edition):

Elvington, Elizabeth Ashcraft Savage. “Contactless Dielectrophoresis towards Drug Screening and Microdevice Development for Cell Sorting.” 2013. Web. 27 Nov 2020.

Vancouver:

Elvington EAS. Contactless Dielectrophoresis towards Drug Screening and Microdevice Development for Cell Sorting. [Internet] [Masters thesis]. Virginia Tech; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10919/23294.

Council of Science Editors:

Elvington EAS. Contactless Dielectrophoresis towards Drug Screening and Microdevice Development for Cell Sorting. [Masters Thesis]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/23294


University of New South Wales

10. Parviz, Maryam. Dual Sensing of Cells Attachment and Spreading using Fluorescence Microscopy and Electrochemical Impedance Spectroscopy.

Degree: Chemistry, 2017, University of New South Wales

 The ambient signals derived from different soluble or physical cues trigger complicated cellular responses that, often, determine the destiny of cells. The task of understanding… (more)

Subjects/Keywords: Drug screening; Impedance; Fluorescence; cell-based biosensor

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APA (6th Edition):

Parviz, M. (2017). Dual Sensing of Cells Attachment and Spreading using Fluorescence Microscopy and Electrochemical Impedance Spectroscopy. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/58121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45417/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Parviz, Maryam. “Dual Sensing of Cells Attachment and Spreading using Fluorescence Microscopy and Electrochemical Impedance Spectroscopy.” 2017. Doctoral Dissertation, University of New South Wales. Accessed November 27, 2020. http://handle.unsw.edu.au/1959.4/58121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45417/SOURCE02?view=true.

MLA Handbook (7th Edition):

Parviz, Maryam. “Dual Sensing of Cells Attachment and Spreading using Fluorescence Microscopy and Electrochemical Impedance Spectroscopy.” 2017. Web. 27 Nov 2020.

Vancouver:

Parviz M. Dual Sensing of Cells Attachment and Spreading using Fluorescence Microscopy and Electrochemical Impedance Spectroscopy. [Internet] [Doctoral dissertation]. University of New South Wales; 2017. [cited 2020 Nov 27]. Available from: http://handle.unsw.edu.au/1959.4/58121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45417/SOURCE02?view=true.

Council of Science Editors:

Parviz M. Dual Sensing of Cells Attachment and Spreading using Fluorescence Microscopy and Electrochemical Impedance Spectroscopy. [Doctoral Dissertation]. University of New South Wales; 2017. Available from: http://handle.unsw.edu.au/1959.4/58121 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:45417/SOURCE02?view=true


University of Utah

11. Gibson, Christopher C. Identification of novel treatments for a hereditary stroke disorder using quantitative phenotypic fingerprinting.

Degree: PhD, Bioengineering, 2014, University of Utah

 Destabilization of the endothelial monolayer lining blood vessels has profound consequences onorganismal homeostasis. Vascular instability plays a well-known role in the pathophysiology of diseasesfrom sepsis… (more)

Subjects/Keywords: Drug discovery; Drug repurposing; Endothelium; High-content; Screening; Stroke

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APA (6th Edition):

Gibson, C. C. (2014). Identification of novel treatments for a hereditary stroke disorder using quantitative phenotypic fingerprinting. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3501/rec/1282

Chicago Manual of Style (16th Edition):

Gibson, Christopher C. “Identification of novel treatments for a hereditary stroke disorder using quantitative phenotypic fingerprinting.” 2014. Doctoral Dissertation, University of Utah. Accessed November 27, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3501/rec/1282.

MLA Handbook (7th Edition):

Gibson, Christopher C. “Identification of novel treatments for a hereditary stroke disorder using quantitative phenotypic fingerprinting.” 2014. Web. 27 Nov 2020.

Vancouver:

Gibson CC. Identification of novel treatments for a hereditary stroke disorder using quantitative phenotypic fingerprinting. [Internet] [Doctoral dissertation]. University of Utah; 2014. [cited 2020 Nov 27]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3501/rec/1282.

Council of Science Editors:

Gibson CC. Identification of novel treatments for a hereditary stroke disorder using quantitative phenotypic fingerprinting. [Doctoral Dissertation]. University of Utah; 2014. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3501/rec/1282


University of Cambridge

12. Chee, Xavier. Rational Development of New Inhibitors of Lipoteichoic Acid Synthase.

Degree: PhD, 2017, University of Cambridge

 Staphyloccocus aureus is an opportunisitic pathogen that causes soft skin and tissue infections (SSTI) such as endocarditis, osteomyelitis and meningitis. In recent years, the re-emergence… (more)

Subjects/Keywords: Virtual screening; Drug discovery; Antibiotics; Antimicrobial resistance; Computational drug design

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APA (6th Edition):

Chee, X. (2017). Rational Development of New Inhibitors of Lipoteichoic Acid Synthase. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/269766

Chicago Manual of Style (16th Edition):

Chee, Xavier. “Rational Development of New Inhibitors of Lipoteichoic Acid Synthase.” 2017. Doctoral Dissertation, University of Cambridge. Accessed November 27, 2020. https://www.repository.cam.ac.uk/handle/1810/269766.

MLA Handbook (7th Edition):

Chee, Xavier. “Rational Development of New Inhibitors of Lipoteichoic Acid Synthase.” 2017. Web. 27 Nov 2020.

Vancouver:

Chee X. Rational Development of New Inhibitors of Lipoteichoic Acid Synthase. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Nov 27]. Available from: https://www.repository.cam.ac.uk/handle/1810/269766.

Council of Science Editors:

Chee X. Rational Development of New Inhibitors of Lipoteichoic Acid Synthase. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/269766


University of Pennsylvania

13. Zhou, Meijia. Identifying Signals Of Potential Drug-Drug Interactions Involving Oral Anticoagulants Using Real World Clinical Data.

Degree: 2019, University of Pennsylvania

Drug-drug interactions (DDIs) with oral anticoagulants may lead to increased risk of serious bleeding and/or thromboembolism. Most oral anticoagulant users are older adults, who are… (more)

Subjects/Keywords: drug-drug interactions; oral anticoagulants; pharmacoepidemiologic screening study; Epidemiology

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APA (6th Edition):

Zhou, M. (2019). Identifying Signals Of Potential Drug-Drug Interactions Involving Oral Anticoagulants Using Real World Clinical Data. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3445

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):

Zhou, Meijia. “Identifying Signals Of Potential Drug-Drug Interactions Involving Oral Anticoagulants Using Real World Clinical Data.” 2019. Thesis, University of Pennsylvania. Accessed November 27, 2020. https://repository.upenn.edu/edissertations/3445.

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

MLA Handbook (7th Edition):

Zhou, Meijia. “Identifying Signals Of Potential Drug-Drug Interactions Involving Oral Anticoagulants Using Real World Clinical Data.” 2019. Web. 27 Nov 2020.

Vancouver:

Zhou M. Identifying Signals Of Potential Drug-Drug Interactions Involving Oral Anticoagulants Using Real World Clinical Data. [Internet] [Thesis]. University of Pennsylvania; 2019. [cited 2020 Nov 27]. Available from: https://repository.upenn.edu/edissertations/3445.

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

Council of Science Editors:

Zhou M. Identifying Signals Of Potential Drug-Drug Interactions Involving Oral Anticoagulants Using Real World Clinical Data. [Thesis]. University of Pennsylvania; 2019. Available from: https://repository.upenn.edu/edissertations/3445

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


University of Toronto

14. Chebotarev, Oleg. High Throughput Microfluidic Platform Capable of Mimicking Key Vascular Microenvironments.

Degree: 2013, University of Toronto

The process of finding a new drug against a chosen target for a vascular disease usually involves high-throughput screening in static multi-well plates. However, due… (more)

Subjects/Keywords: Microfluidics; High throughput screening; Drug Screening; Monocyte adhesion; TNF-alpha; 0548; 0541

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APA (6th Edition):

Chebotarev, O. (2013). High Throughput Microfluidic Platform Capable of Mimicking Key Vascular Microenvironments. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/69980

Chicago Manual of Style (16th Edition):

Chebotarev, Oleg. “High Throughput Microfluidic Platform Capable of Mimicking Key Vascular Microenvironments.” 2013. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/69980.

MLA Handbook (7th Edition):

Chebotarev, Oleg. “High Throughput Microfluidic Platform Capable of Mimicking Key Vascular Microenvironments.” 2013. Web. 27 Nov 2020.

Vancouver:

Chebotarev O. High Throughput Microfluidic Platform Capable of Mimicking Key Vascular Microenvironments. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/69980.

Council of Science Editors:

Chebotarev O. High Throughput Microfluidic Platform Capable of Mimicking Key Vascular Microenvironments. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/69980


University of Cambridge

15. Collins, Súil. The identification and development of small molecule inhibitors of amyloid β aggregation.

Degree: PhD, 2017, University of Cambridge

 Amyloid β (1-42) (Aβ42) is a seminal neuropathic agent in Alzheimer’s disease (AD), a multifaceted neurodegenerative disorder for which no preventative measures or disease modifying… (more)

Subjects/Keywords: 612.8; amyloid beta; aggregation inhibitiors; protein aggregation; fluorescence lifetime imaging microscopy; microfluidic screening; drug screening

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APA (6th Edition):

Collins, S. (2017). The identification and development of small molecule inhibitors of amyloid β aggregation. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047

Chicago Manual of Style (16th Edition):

Collins, Súil. “The identification and development of small molecule inhibitors of amyloid β aggregation.” 2017. Doctoral Dissertation, University of Cambridge. Accessed November 27, 2020. https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047.

MLA Handbook (7th Edition):

Collins, Súil. “The identification and development of small molecule inhibitors of amyloid β aggregation.” 2017. Web. 27 Nov 2020.

Vancouver:

Collins S. The identification and development of small molecule inhibitors of amyloid β aggregation. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Nov 27]. Available from: https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047.

Council of Science Editors:

Collins S. The identification and development of small molecule inhibitors of amyloid β aggregation. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047


Texas A&M University

16. Powell, Reid Trenton. Extracting Biological Knowledge from High Throughput Phenotypic Screens.

Degree: PhD, Medical Sciences, 2018, Texas A&M University

 High throughput drug screening has greatly progressed drug discovery for diseases such as cancer. Specifically, the introduction of the automated microscope in high throughput drug(more)

Subjects/Keywords: high throughput screening; cell-based assays; phenotypic screening; high content analysis; bioinformatics' drug discovery; drug development

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APA (6th Edition):

Powell, R. T. (2018). Extracting Biological Knowledge from High Throughput Phenotypic Screens. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173989

Chicago Manual of Style (16th Edition):

Powell, Reid Trenton. “Extracting Biological Knowledge from High Throughput Phenotypic Screens.” 2018. Doctoral Dissertation, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/173989.

MLA Handbook (7th Edition):

Powell, Reid Trenton. “Extracting Biological Knowledge from High Throughput Phenotypic Screens.” 2018. Web. 27 Nov 2020.

Vancouver:

Powell RT. Extracting Biological Knowledge from High Throughput Phenotypic Screens. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/173989.

Council of Science Editors:

Powell RT. Extracting Biological Knowledge from High Throughput Phenotypic Screens. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173989


KTH

17. Talts, Ülle-Linda. Characterization of graphene-based sensors for forensic applications : Evaluating suitability of CVD graphene-based resistive sensor for detection of amphetamine.

Degree: Electrical Engineering and Computer Science (EECS), 2019, KTH

Recent improvements in sensor technology and applications can be partly attributed to the advancements in microand nanoscale fabrication processes and discovery of novel materials.… (more)

Subjects/Keywords: Sensor systems; Chemical sensors; Nanosensors; Drug screening; Nanomaterials; Sensorsystem; Kemiska sensorer; Nanosensorer; Drug screening; Nanomaterial; Nano Technology; Nanoteknik

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APA (6th Edition):

Talts, . (2019). Characterization of graphene-based sensors for forensic applications : Evaluating suitability of CVD graphene-based resistive sensor for detection of amphetamine. (Thesis). KTH. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-271188

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):

Talts, Ülle-Linda. “Characterization of graphene-based sensors for forensic applications : Evaluating suitability of CVD graphene-based resistive sensor for detection of amphetamine.” 2019. Thesis, KTH. Accessed November 27, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-271188.

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

MLA Handbook (7th Edition):

Talts, Ülle-Linda. “Characterization of graphene-based sensors for forensic applications : Evaluating suitability of CVD graphene-based resistive sensor for detection of amphetamine.” 2019. Web. 27 Nov 2020.

Vancouver:

Talts . Characterization of graphene-based sensors for forensic applications : Evaluating suitability of CVD graphene-based resistive sensor for detection of amphetamine. [Internet] [Thesis]. KTH; 2019. [cited 2020 Nov 27]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-271188.

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

Council of Science Editors:

Talts . Characterization of graphene-based sensors for forensic applications : Evaluating suitability of CVD graphene-based resistive sensor for detection of amphetamine. [Thesis]. KTH; 2019. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-271188

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


Virginia Commonwealth University

18. Smith, Courtney. Indirect Screening: Enhancing Identification of Illicit Drug Use during Pregnancy.

Degree: PhD, Psychology, 2011, Virginia Commonwealth University

 OBJECTIVE: Most drug use screening measures rely on and are validated against self-report. Fear of negative consequences often promotes denial of drug use. For pregnant… (more)

Subjects/Keywords: pregnancy; drug use; screening; prenatal drug use; Psychology; Social and Behavioral Sciences

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APA (6th Edition):

Smith, C. (2011). Indirect Screening: Enhancing Identification of Illicit Drug Use during Pregnancy. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/42J6-FR29 ; https://scholarscompass.vcu.edu/etd/2693

Chicago Manual of Style (16th Edition):

Smith, Courtney. “Indirect Screening: Enhancing Identification of Illicit Drug Use during Pregnancy.” 2011. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 27, 2020. https://doi.org/10.25772/42J6-FR29 ; https://scholarscompass.vcu.edu/etd/2693.

MLA Handbook (7th Edition):

Smith, Courtney. “Indirect Screening: Enhancing Identification of Illicit Drug Use during Pregnancy.” 2011. Web. 27 Nov 2020.

Vancouver:

Smith C. Indirect Screening: Enhancing Identification of Illicit Drug Use during Pregnancy. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2011. [cited 2020 Nov 27]. Available from: https://doi.org/10.25772/42J6-FR29 ; https://scholarscompass.vcu.edu/etd/2693.

Council of Science Editors:

Smith C. Indirect Screening: Enhancing Identification of Illicit Drug Use during Pregnancy. [Doctoral Dissertation]. Virginia Commonwealth University; 2011. Available from: https://doi.org/10.25772/42J6-FR29 ; https://scholarscompass.vcu.edu/etd/2693


University of Manchester

19. Taylor, Jessica Tanya. High throughput screening of patient specific tumour cells: towards personalised treatment in recurrent glioblastoma multiforme.

Degree: 2019, University of Manchester

 Glioblastoma Multiforme is the most common adult primary brain tumour, with median survival rates of around 15 months. The aggressive and heterogeneous nature of this… (more)

Subjects/Keywords: glioblastoma; neuro oncology; drug repurposing; personalised medicine; drug screening; mouse models; brain tumours; cancer research

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APA (6th Edition):

Taylor, J. T. (2019). High throughput screening of patient specific tumour cells: towards personalised treatment in recurrent glioblastoma multiforme. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319176

Chicago Manual of Style (16th Edition):

Taylor, Jessica Tanya. “High throughput screening of patient specific tumour cells: towards personalised treatment in recurrent glioblastoma multiforme.” 2019. Doctoral Dissertation, University of Manchester. Accessed November 27, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319176.

MLA Handbook (7th Edition):

Taylor, Jessica Tanya. “High throughput screening of patient specific tumour cells: towards personalised treatment in recurrent glioblastoma multiforme.” 2019. Web. 27 Nov 2020.

Vancouver:

Taylor JT. High throughput screening of patient specific tumour cells: towards personalised treatment in recurrent glioblastoma multiforme. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Nov 27]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319176.

Council of Science Editors:

Taylor JT. High throughput screening of patient specific tumour cells: towards personalised treatment in recurrent glioblastoma multiforme. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319176


University of Manchester

20. Taylor, Jessica. High throughput screening of patient specific tumour cells : towards personalised treatment in recurrent glioblastoma multiforme.

Degree: PhD, 2019, University of Manchester

 Glioblastoma Multiforme is the most common adult primary brain tumour, with median survival rates of around 15 months. The aggressive and heterogeneous nature of this… (more)

Subjects/Keywords: mouse models; cancer research; brain tumours; drug screening; personalised medicine; drug repurposing; neuro oncology; glioblastoma

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APA (6th Edition):

Taylor, J. (2019). High throughput screening of patient specific tumour cells : towards personalised treatment in recurrent glioblastoma multiforme. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/high-throughput-screening-of-patient-specific-tumour-cells-towards-personalised-treatment-in-recurrent-glioblastoma-multiforme(f4b3043c-faf0-4298-9b9f-2adb6a9577b6).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.809321

Chicago Manual of Style (16th Edition):

Taylor, Jessica. “High throughput screening of patient specific tumour cells : towards personalised treatment in recurrent glioblastoma multiforme.” 2019. Doctoral Dissertation, University of Manchester. Accessed November 27, 2020. https://www.research.manchester.ac.uk/portal/en/theses/high-throughput-screening-of-patient-specific-tumour-cells-towards-personalised-treatment-in-recurrent-glioblastoma-multiforme(f4b3043c-faf0-4298-9b9f-2adb6a9577b6).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.809321.

MLA Handbook (7th Edition):

Taylor, Jessica. “High throughput screening of patient specific tumour cells : towards personalised treatment in recurrent glioblastoma multiforme.” 2019. Web. 27 Nov 2020.

Vancouver:

Taylor J. High throughput screening of patient specific tumour cells : towards personalised treatment in recurrent glioblastoma multiforme. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Nov 27]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/high-throughput-screening-of-patient-specific-tumour-cells-towards-personalised-treatment-in-recurrent-glioblastoma-multiforme(f4b3043c-faf0-4298-9b9f-2adb6a9577b6).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.809321.

Council of Science Editors:

Taylor J. High throughput screening of patient specific tumour cells : towards personalised treatment in recurrent glioblastoma multiforme. [Doctoral Dissertation]. University of Manchester; 2019. Available from: https://www.research.manchester.ac.uk/portal/en/theses/high-throughput-screening-of-patient-specific-tumour-cells-towards-personalised-treatment-in-recurrent-glioblastoma-multiforme(f4b3043c-faf0-4298-9b9f-2adb6a9577b6).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.809321


The Ohio State University

21. Mahasenan, Kiran V. Discovery of novel small molecule enzyme inhibitors and receptor modulators through structure-based computational design.

Degree: PhD, Pharmacy, 2012, The Ohio State University

 Discovery of novel drug candidates for a particular disease condition has traditionally been carried out by experimentally screening thousands of compounds for desired activity in… (more)

Subjects/Keywords: Pharmaceuticals; Pharmacy Sciences; structure-based drug design; computer-aided drug design; virtual screening; protein modeling

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APA (6th Edition):

Mahasenan, K. V. (2012). Discovery of novel small molecule enzyme inhibitors and receptor modulators through structure-based computational design. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1332367560

Chicago Manual of Style (16th Edition):

Mahasenan, Kiran V. “Discovery of novel small molecule enzyme inhibitors and receptor modulators through structure-based computational design.” 2012. Doctoral Dissertation, The Ohio State University. Accessed November 27, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1332367560.

MLA Handbook (7th Edition):

Mahasenan, Kiran V. “Discovery of novel small molecule enzyme inhibitors and receptor modulators through structure-based computational design.” 2012. Web. 27 Nov 2020.

Vancouver:

Mahasenan KV. Discovery of novel small molecule enzyme inhibitors and receptor modulators through structure-based computational design. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2020 Nov 27]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1332367560.

Council of Science Editors:

Mahasenan KV. Discovery of novel small molecule enzyme inhibitors and receptor modulators through structure-based computational design. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1332367560


University of California – Santa Cruz

22. 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 November 27, 2020. 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. 27 Nov 2020.

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 2020 Nov 27]. 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

23. 小関, 祐司. Identification of Novel Compounds with Anti-Mycobacterial Activity Using in Silico Screening and Pharmacophore Modeling Targeting Mycobacterium Thymidine Monophosphate Kinase.

Degree: 博士(情報工学), 2017, Kyushu Institute of Technology / 九州工業大学

The increasing prevalence of drug-resistant tuberculosis (TB), which is resistant to effective multiple antibiotic, remains a major public health menace. The Mycobacterium tuberculosis (M. tuberculosis)… (more)

Subjects/Keywords: In silico drug screening; Molecular Dynamics; Mycobacterium; Pharmacophore Modeling; TMPK

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APA (6th Edition):

小関, . (2017). Identification of Novel Compounds with Anti-Mycobacterial Activity Using in Silico Screening and Pharmacophore Modeling Targeting Mycobacterium Thymidine Monophosphate Kinase. (Thesis). Kyushu Institute of Technology / 九州工業大学. Retrieved from http://hdl.handle.net/10228/5456

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):

小関, 祐司. “Identification of Novel Compounds with Anti-Mycobacterial Activity Using in Silico Screening and Pharmacophore Modeling Targeting Mycobacterium Thymidine Monophosphate Kinase.” 2017. Thesis, Kyushu Institute of Technology / 九州工業大学. Accessed November 27, 2020. http://hdl.handle.net/10228/5456.

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

MLA Handbook (7th Edition):

小関, 祐司. “Identification of Novel Compounds with Anti-Mycobacterial Activity Using in Silico Screening and Pharmacophore Modeling Targeting Mycobacterium Thymidine Monophosphate Kinase.” 2017. Web. 27 Nov 2020.

Vancouver:

小関 . Identification of Novel Compounds with Anti-Mycobacterial Activity Using in Silico Screening and Pharmacophore Modeling Targeting Mycobacterium Thymidine Monophosphate Kinase. [Internet] [Thesis]. Kyushu Institute of Technology / 九州工業大学; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10228/5456.

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

Council of Science Editors:

小関 . Identification of Novel Compounds with Anti-Mycobacterial Activity Using in Silico Screening and Pharmacophore Modeling Targeting Mycobacterium Thymidine Monophosphate Kinase. [Thesis]. Kyushu Institute of Technology / 九州工業大学; 2017. Available from: http://hdl.handle.net/10228/5456

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

24. Pal, Rajarshi. Evaluation of the potential of embryonic stem cells esc and their derivatives as a model for drug screening and toxicity;.

Degree:  – , 2012, Manipal University

The present thesis focuses on the evaluation of human embryonic stem cells (hESC) as a model to understand the propensity of independently derived cell lines… (more)

Subjects/Keywords: Embryonic Stem Cells; Embryoid Bodies; Hepatocyte Differentiation; Cytotoxicity; Drug Screening

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APA (6th Edition):

Pal, R. (2012). Evaluation of the potential of embryonic stem cells esc and their derivatives as a model for drug screening and toxicity;. (Thesis). Manipal University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/5003

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):

Pal, Rajarshi. “Evaluation of the potential of embryonic stem cells esc and their derivatives as a model for drug screening and toxicity;.” 2012. Thesis, Manipal University. Accessed November 27, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/5003.

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

MLA Handbook (7th Edition):

Pal, Rajarshi. “Evaluation of the potential of embryonic stem cells esc and their derivatives as a model for drug screening and toxicity;.” 2012. Web. 27 Nov 2020.

Vancouver:

Pal R. Evaluation of the potential of embryonic stem cells esc and their derivatives as a model for drug screening and toxicity;. [Internet] [Thesis]. Manipal University; 2012. [cited 2020 Nov 27]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/5003.

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

Council of Science Editors:

Pal R. Evaluation of the potential of embryonic stem cells esc and their derivatives as a model for drug screening and toxicity;. [Thesis]. Manipal University; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/5003

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


Texas A&M University

25. 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 November 27, 2020. 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. 27 Nov 2020.

Vancouver:

LaiHing S1. Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis. [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2020 Nov 27]. 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


McMaster University

26. Hirmiz, Nehad. DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS.

Degree: 2019, McMaster University

Protein-protein interactions are important for biological processes. Therefore, many small molecules target a specific protein or interaction in the cell to have biological consequence. While… (more)

Subjects/Keywords: Fluorescence Microscopy; Confocal Microsopy; Fluorescence Lifetime; Rapid Imaging; Drug Screening

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APA (6th Edition):

Hirmiz, N. (2019). DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS. (Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/25137

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):

Hirmiz, Nehad. “DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS.” 2019. Thesis, McMaster University. Accessed November 27, 2020. http://hdl.handle.net/11375/25137.

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

MLA Handbook (7th Edition):

Hirmiz, Nehad. “DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS.” 2019. Web. 27 Nov 2020.

Vancouver:

Hirmiz N. DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS. [Internet] [Thesis]. McMaster University; 2019. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/11375/25137.

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

Council of Science Editors:

Hirmiz N. DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS. [Thesis]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/25137

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


University of Toronto

27. Conant, Genevieve Ann. High Throughput Screening of Kinase Inhibitor Drugs on Cardiac Function using Engineered Heart Tissue Constructs.

Degree: 2017, University of Toronto

Protein kinase inhibitors (KIs) are used as highly specific cancer targeting agents for their ability to prevent kinase molecules from activating signalling pathways that regulate… (more)

Subjects/Keywords: Engineered cardiac tissue; Kinase inhibitors; Pre-clinical drug screening; 0541

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APA (6th Edition):

Conant, G. A. (2017). High Throughput Screening of Kinase Inhibitor Drugs on Cardiac Function using Engineered Heart Tissue Constructs. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89959

Chicago Manual of Style (16th Edition):

Conant, Genevieve Ann. “High Throughput Screening of Kinase Inhibitor Drugs on Cardiac Function using Engineered Heart Tissue Constructs.” 2017. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/89959.

MLA Handbook (7th Edition):

Conant, Genevieve Ann. “High Throughput Screening of Kinase Inhibitor Drugs on Cardiac Function using Engineered Heart Tissue Constructs.” 2017. Web. 27 Nov 2020.

Vancouver:

Conant GA. High Throughput Screening of Kinase Inhibitor Drugs on Cardiac Function using Engineered Heart Tissue Constructs. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/89959.

Council of Science Editors:

Conant GA. High Throughput Screening of Kinase Inhibitor Drugs on Cardiac Function using Engineered Heart Tissue Constructs. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/89959


University of Wollongong

28. Rashad Ahmed, Adel Ahmed. The medicinal chemistry development for new antimicrobial chemotherapeutics.

Degree: PhD, 2014, University of Wollongong

  Chapter 2 discusses the synthesis of the arenearylpyrimidylmethanes (AAPMs) series was investigated to further develop the structure activity relationships (SAR) of these compounds as… (more)

Subjects/Keywords: Chikungunya virus; antiviral drug design; virtual screening; African sleeping sickness

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APA (6th Edition):

Rashad Ahmed, A. A. (2014). The medicinal chemistry development for new antimicrobial chemotherapeutics. (Doctoral Dissertation). University of Wollongong. Retrieved from 030401 Biologically Active Molecules, 030402 Biomolecular Modelling and Design, 030403 Characterisation of Biological Macromolecules ; https://ro.uow.edu.au/theses/4132

Chicago Manual of Style (16th Edition):

Rashad Ahmed, Adel Ahmed. “The medicinal chemistry development for new antimicrobial chemotherapeutics.” 2014. Doctoral Dissertation, University of Wollongong. Accessed November 27, 2020. 030401 Biologically Active Molecules, 030402 Biomolecular Modelling and Design, 030403 Characterisation of Biological Macromolecules ; https://ro.uow.edu.au/theses/4132.

MLA Handbook (7th Edition):

Rashad Ahmed, Adel Ahmed. “The medicinal chemistry development for new antimicrobial chemotherapeutics.” 2014. Web. 27 Nov 2020.

Vancouver:

Rashad Ahmed AA. The medicinal chemistry development for new antimicrobial chemotherapeutics. [Internet] [Doctoral dissertation]. University of Wollongong; 2014. [cited 2020 Nov 27]. Available from: 030401 Biologically Active Molecules, 030402 Biomolecular Modelling and Design, 030403 Characterisation of Biological Macromolecules ; https://ro.uow.edu.au/theses/4132.

Council of Science Editors:

Rashad Ahmed AA. The medicinal chemistry development for new antimicrobial chemotherapeutics. [Doctoral Dissertation]. University of Wollongong; 2014. Available from: 030401 Biologically Active Molecules, 030402 Biomolecular Modelling and Design, 030403 Characterisation of Biological Macromolecules ; https://ro.uow.edu.au/theses/4132


University of Cambridge

29. Lago Cooke, Santiago Guillermo. A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO.

Degree: PhD, 2016, University of Cambridge

 The current work entails the development of a novel high content platform for the measurement of kinetic ligand responses across cell signalling networks at the… (more)

Subjects/Keywords: drug discovery; neuropsychiatric disorders; high-content screening; single-cell; signalling network

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

APA (6th Edition):

Lago Cooke, S. G. (2016). A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/270297

Chicago Manual of Style (16th Edition):

Lago Cooke, Santiago Guillermo. “A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO.” 2016. Doctoral Dissertation, University of Cambridge. Accessed November 27, 2020. https://www.repository.cam.ac.uk/handle/1810/270297.

MLA Handbook (7th Edition):

Lago Cooke, Santiago Guillermo. “A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO.” 2016. Web. 27 Nov 2020.

Vancouver:

Lago Cooke SG. A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO. [Internet] [Doctoral dissertation]. University of Cambridge; 2016. [cited 2020 Nov 27]. Available from: https://www.repository.cam.ac.uk/handle/1810/270297.

Council of Science Editors:

Lago Cooke SG. A NOVEL PIPELINE FOR DRUG DISCOVERY IN NEUROPSYCHIATRIC DISORDERS USING HIGH-CONTENT SINGLE-CELL SCREENING OF SIGNALLING NETWORK RESPONSES EX VIVO. [Doctoral Dissertation]. University of Cambridge; 2016. Available from: https://www.repository.cam.ac.uk/handle/1810/270297


Universitat Autònoma de Barcelona

30. Tunca, Guzin. A virtual screening procedure combining pharmacophore filtering and molecular docking with the LIE method.

Degree: Departament de Medicina, 2012, Universitat Autònoma de Barcelona

 Virtual screening plays a central role in the world of drug discovery today. In silico testing allows to screen millions of small molecules and to… (more)

Subjects/Keywords: Drug discovery; Virtual screening; Ligand binding; Ciències de la Salut; 577

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

APA (6th Edition):

Tunca, G. (2012). A virtual screening procedure combining pharmacophore filtering and molecular docking with the LIE method. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/284031

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):

Tunca, Guzin. “A virtual screening procedure combining pharmacophore filtering and molecular docking with the LIE method.” 2012. Thesis, Universitat Autònoma de Barcelona. Accessed November 27, 2020. http://hdl.handle.net/10803/284031.

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

MLA Handbook (7th Edition):

Tunca, Guzin. “A virtual screening procedure combining pharmacophore filtering and molecular docking with the LIE method.” 2012. Web. 27 Nov 2020.

Vancouver:

Tunca G. A virtual screening procedure combining pharmacophore filtering and molecular docking with the LIE method. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10803/284031.

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

Council of Science Editors:

Tunca G. A virtual screening procedure combining pharmacophore filtering and molecular docking with the LIE method. [Thesis]. Universitat Autònoma de Barcelona; 2012. Available from: http://hdl.handle.net/10803/284031

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

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