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You searched for subject:(DRUG INTERACTION). Showing records 1 – 30 of 185 total matches.

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Penn State University

1. Davaasuren, Dolzodmaa. Analysis of Opioid Related Adverse Events and Signal Detection with Machine Learning.

Degree: 2019, Penn State University

 In the past 30 years, the United States has experienced an unprecedented opioid epidemic. It’s been reported that physicians dispense more than 650,000 opioid prescriptions… (more)

Subjects/Keywords: Opioid drugs; Adverse Drug Events; Adverse Drug Reactions; Drug-Drug Interaction

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

APA (6th Edition):

Davaasuren, D. (2019). Analysis of Opioid Related Adverse Events and Signal Detection with Machine Learning. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/16880dud240

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):

Davaasuren, Dolzodmaa. “Analysis of Opioid Related Adverse Events and Signal Detection with Machine Learning.” 2019. Thesis, Penn State University. Accessed January 19, 2021. https://submit-etda.libraries.psu.edu/catalog/16880dud240.

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

MLA Handbook (7th Edition):

Davaasuren, Dolzodmaa. “Analysis of Opioid Related Adverse Events and Signal Detection with Machine Learning.” 2019. Web. 19 Jan 2021.

Vancouver:

Davaasuren D. Analysis of Opioid Related Adverse Events and Signal Detection with Machine Learning. [Internet] [Thesis]. Penn State University; 2019. [cited 2021 Jan 19]. Available from: https://submit-etda.libraries.psu.edu/catalog/16880dud240.

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

Council of Science Editors:

Davaasuren D. Analysis of Opioid Related Adverse Events and Signal Detection with Machine Learning. [Thesis]. Penn State University; 2019. Available from: https://submit-etda.libraries.psu.edu/catalog/16880dud240

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


University of Illinois – Urbana-Champaign

2. Haghighat Jahromi, Amin. Advances in myotonic dystrophy type 1 drug discovery through design of novel ligands and mechanism establishment.

Degree: PhD, 0319, 2013, University of Illinois – Urbana-Champaign

 Myotonic dystrophy type 1 (DM1) is caused by an expanded CUG repeat (CUGexp) that sequesters muscleblind-like 1 protein (MBNL1), a protein that regulates alternative splicing.… (more)

Subjects/Keywords: Myotonic Dystrophy; Drug discovery; MBNL1-CUGexp interaction

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APA (6th Edition):

Haghighat Jahromi, A. (2013). Advances in myotonic dystrophy type 1 drug discovery through design of novel ligands and mechanism establishment. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/44815

Chicago Manual of Style (16th Edition):

Haghighat Jahromi, Amin. “Advances in myotonic dystrophy type 1 drug discovery through design of novel ligands and mechanism establishment.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 19, 2021. http://hdl.handle.net/2142/44815.

MLA Handbook (7th Edition):

Haghighat Jahromi, Amin. “Advances in myotonic dystrophy type 1 drug discovery through design of novel ligands and mechanism establishment.” 2013. Web. 19 Jan 2021.

Vancouver:

Haghighat Jahromi A. Advances in myotonic dystrophy type 1 drug discovery through design of novel ligands and mechanism establishment. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2142/44815.

Council of Science Editors:

Haghighat Jahromi A. Advances in myotonic dystrophy type 1 drug discovery through design of novel ligands and mechanism establishment. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/44815

3. Miyakawa, Sachiko. Short-term drug–drug interaction between sildenafil and bosentan under long-term use in patients with pulmonary arterial hypertension : 肺動脈性肺高血圧症患者における長期的なシルデナフィルとボセンタン使用下での両薬物の短期的薬物間相互作用.

Degree: 博士(医学), 2014, Hamamatsu University School of Medicine / 浜松医科大学

Sildenafil and bosentan are often co-administered for pulmonary arterial hypertension (PAH) treatment. The plasma concentration of sildenafil can be decreased by half if co-administered with… (more)

Subjects/Keywords: Drug-Drug Interaction; Pulmonary Arterial Hypertension; Sildenafil; Bosentan; Pharmacokinetics

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APA (6th Edition):

Miyakawa, S. (2014). Short-term drug–drug interaction between sildenafil and bosentan under long-term use in patients with pulmonary arterial hypertension : 肺動脈性肺高血圧症患者における長期的なシルデナフィルとボセンタン使用下での両薬物の短期的薬物間相互作用. (Thesis). Hamamatsu University School of Medicine / 浜松医科大学. Retrieved from http://hdl.handle.net/10271/2783

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):

Miyakawa, Sachiko. “Short-term drug–drug interaction between sildenafil and bosentan under long-term use in patients with pulmonary arterial hypertension : 肺動脈性肺高血圧症患者における長期的なシルデナフィルとボセンタン使用下での両薬物の短期的薬物間相互作用.” 2014. Thesis, Hamamatsu University School of Medicine / 浜松医科大学. Accessed January 19, 2021. http://hdl.handle.net/10271/2783.

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

MLA Handbook (7th Edition):

Miyakawa, Sachiko. “Short-term drug–drug interaction between sildenafil and bosentan under long-term use in patients with pulmonary arterial hypertension : 肺動脈性肺高血圧症患者における長期的なシルデナフィルとボセンタン使用下での両薬物の短期的薬物間相互作用.” 2014. Web. 19 Jan 2021.

Vancouver:

Miyakawa S. Short-term drug–drug interaction between sildenafil and bosentan under long-term use in patients with pulmonary arterial hypertension : 肺動脈性肺高血圧症患者における長期的なシルデナフィルとボセンタン使用下での両薬物の短期的薬物間相互作用. [Internet] [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2014. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10271/2783.

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

Council of Science Editors:

Miyakawa S. Short-term drug–drug interaction between sildenafil and bosentan under long-term use in patients with pulmonary arterial hypertension : 肺動脈性肺高血圧症患者における長期的なシルデナフィルとボセンタン使用下での両薬物の短期的薬物間相互作用. [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2014. Available from: http://hdl.handle.net/10271/2783

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


Dalhousie University

4. Alabdulhafith, Maali. NFC-Enabled Smartphone Application for Drug Interaction and Drug Allergy Detection.

Degree: Master of Computer Science, Faculty of Computer Science, 2012, Dalhousie University

The system has been implemented using Samsung Nexus S smartphone with Android 2.3.6 platform, MIFARE Classic 1K tags, and a database populated with 10 patients’… (more)

Subjects/Keywords: NFC; Smartphone; Morbidity; Drug Allergy; Drug Interaction; Medication Errors

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APA (6th Edition):

Alabdulhafith, M. (2012). NFC-Enabled Smartphone Application for Drug Interaction and Drug Allergy Detection. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15500

Chicago Manual of Style (16th Edition):

Alabdulhafith, Maali. “NFC-Enabled Smartphone Application for Drug Interaction and Drug Allergy Detection.” 2012. Masters Thesis, Dalhousie University. Accessed January 19, 2021. http://hdl.handle.net/10222/15500.

MLA Handbook (7th Edition):

Alabdulhafith, Maali. “NFC-Enabled Smartphone Application for Drug Interaction and Drug Allergy Detection.” 2012. Web. 19 Jan 2021.

Vancouver:

Alabdulhafith M. NFC-Enabled Smartphone Application for Drug Interaction and Drug Allergy Detection. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10222/15500.

Council of Science Editors:

Alabdulhafith M. NFC-Enabled Smartphone Application for Drug Interaction and Drug Allergy Detection. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15500


Vanderbilt University

5. Crouch, Rachel Denise. Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics.

Degree: PhD, Pharmacology, 2016, Vanderbilt University

 Unacceptable pharmacokinetics (PK) relating to aldehyde oxidase (AO) metabolism have resulted in clinical failure of several promising drug candidates, yet reliable and standardized methods to… (more)

Subjects/Keywords: aldehyde oxidase; allometric scaling; drug metabolism; pharmacokinetics; drug interaction

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APA (6th Edition):

Crouch, R. D. (2016). Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14636

Chicago Manual of Style (16th Edition):

Crouch, Rachel Denise. “Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 19, 2021. http://hdl.handle.net/1803/14636.

MLA Handbook (7th Edition):

Crouch, Rachel Denise. “Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics.” 2016. Web. 19 Jan 2021.

Vancouver:

Crouch RD. Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1803/14636.

Council of Science Editors:

Crouch RD. Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/14636


University of Illinois – Chicago

6. Qiu, Xi. Chemoprevention Study of Botanical Dietary Supplements by Mass Spectrometry.

Degree: 2012, University of Illinois – Chicago

 Botanical dietary supplements have the potential to maintain and or even improve health. In particular, some botanical dietary supplements have the potential to prevent cancer.… (more)

Subjects/Keywords: Chemoprevention; dietary supplement; quantitative proteomics; drug-drug interaction; botanical safety evaluation

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APA (6th Edition):

Qiu, X. (2012). Chemoprevention Study of Botanical Dietary Supplements by Mass Spectrometry. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9309

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):

Qiu, Xi. “Chemoprevention Study of Botanical Dietary Supplements by Mass Spectrometry.” 2012. Thesis, University of Illinois – Chicago. Accessed January 19, 2021. http://hdl.handle.net/10027/9309.

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

MLA Handbook (7th Edition):

Qiu, Xi. “Chemoprevention Study of Botanical Dietary Supplements by Mass Spectrometry.” 2012. Web. 19 Jan 2021.

Vancouver:

Qiu X. Chemoprevention Study of Botanical Dietary Supplements by Mass Spectrometry. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10027/9309.

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

Council of Science Editors:

Qiu X. Chemoprevention Study of Botanical Dietary Supplements by Mass Spectrometry. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9309

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

7. Björn, Niklas. Database processing for identification of concomitant drug frequencies in a forensic material positive for antidepressant drugs.

Degree: Faculty of Health Sciences, 2014, Linköping UniversityLinköping University

  This article presents a study conducted on data containing drug concentrations. The data was obtained from femoral venous blood samples collected at medico legal… (more)

Subjects/Keywords: TCA; TeCA; SSRI; SNRI; MAOI; antidepressant drug; drug interaction; intoxication

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APA (6th Edition):

Björn, N. (2014). Database processing for identification of concomitant drug frequencies in a forensic material positive for antidepressant drugs. (Thesis). Linköping UniversityLinköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-107575

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):

Björn, Niklas. “Database processing for identification of concomitant drug frequencies in a forensic material positive for antidepressant drugs.” 2014. Thesis, Linköping UniversityLinköping University. Accessed January 19, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-107575.

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

MLA Handbook (7th Edition):

Björn, Niklas. “Database processing for identification of concomitant drug frequencies in a forensic material positive for antidepressant drugs.” 2014. Web. 19 Jan 2021.

Vancouver:

Björn N. Database processing for identification of concomitant drug frequencies in a forensic material positive for antidepressant drugs. [Internet] [Thesis]. Linköping UniversityLinköping University; 2014. [cited 2021 Jan 19]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-107575.

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

Council of Science Editors:

Björn N. Database processing for identification of concomitant drug frequencies in a forensic material positive for antidepressant drugs. [Thesis]. Linköping UniversityLinköping University; 2014. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-107575

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


University of Washington

8. Stevison, Faith M. In Vitro to In Vivo Translation of Complex Drug-Drug Interactions Involving Retinoic Acid.

Degree: PhD, 2018, University of Washington

 all-trans-retinoic acid (atRA), the active metabolite of vitamin A, is a ligand for several nuclear receptors and acts as a critical regulator of many physiological… (more)

Subjects/Keywords: CYP26; CYP2D6; drug-drug interaction; pharmacokinetics; retinoic acid; Pharmaceutical sciences; Pharmaceutics

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APA (6th Edition):

Stevison, F. M. (2018). In Vitro to In Vivo Translation of Complex Drug-Drug Interactions Involving Retinoic Acid. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43124

Chicago Manual of Style (16th Edition):

Stevison, Faith M. “In Vitro to In Vivo Translation of Complex Drug-Drug Interactions Involving Retinoic Acid.” 2018. Doctoral Dissertation, University of Washington. Accessed January 19, 2021. http://hdl.handle.net/1773/43124.

MLA Handbook (7th Edition):

Stevison, Faith M. “In Vitro to In Vivo Translation of Complex Drug-Drug Interactions Involving Retinoic Acid.” 2018. Web. 19 Jan 2021.

Vancouver:

Stevison FM. In Vitro to In Vivo Translation of Complex Drug-Drug Interactions Involving Retinoic Acid. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1773/43124.

Council of Science Editors:

Stevison FM. In Vitro to In Vivo Translation of Complex Drug-Drug Interactions Involving Retinoic Acid. [Doctoral Dissertation]. University of Washington; 2018. Available from: http://hdl.handle.net/1773/43124


University of Washington

9. McFeely, Savannah Jane Kerr. Clinical Significance and Regulatory Framework for the Evaluation of Organic Anion Transporting Polypeptide 1B-Based Drug-Drug Interactions.

Degree: PhD, 2019, University of Washington

 This dissertation research aims to conduct a comprehensive analysis of the clinical role of organic anion transporting polypeptides (OATPs) 1B1 and 1B3 and the regulatory… (more)

Subjects/Keywords: drug-drug interaction; OATP; transporters; Pharmaceutical sciences; Pharmaceutics

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APA (6th Edition):

McFeely, S. J. K. (2019). Clinical Significance and Regulatory Framework for the Evaluation of Organic Anion Transporting Polypeptide 1B-Based Drug-Drug Interactions. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/44421

Chicago Manual of Style (16th Edition):

McFeely, Savannah Jane Kerr. “Clinical Significance and Regulatory Framework for the Evaluation of Organic Anion Transporting Polypeptide 1B-Based Drug-Drug Interactions.” 2019. Doctoral Dissertation, University of Washington. Accessed January 19, 2021. http://hdl.handle.net/1773/44421.

MLA Handbook (7th Edition):

McFeely, Savannah Jane Kerr. “Clinical Significance and Regulatory Framework for the Evaluation of Organic Anion Transporting Polypeptide 1B-Based Drug-Drug Interactions.” 2019. Web. 19 Jan 2021.

Vancouver:

McFeely SJK. Clinical Significance and Regulatory Framework for the Evaluation of Organic Anion Transporting Polypeptide 1B-Based Drug-Drug Interactions. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1773/44421.

Council of Science Editors:

McFeely SJK. Clinical Significance and Regulatory Framework for the Evaluation of Organic Anion Transporting Polypeptide 1B-Based Drug-Drug Interactions. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/44421

10. D'Cunha, Ronilda Raymond. Treatment strategies to reverse efflux transporter-mediated resistance to Tyrosine kinase inhibitors.

Degree: PhD, Pharmacy, 2018, University of Iowa

  Multidrug resistance (MDR), a phenomenon in which tumors that were initially sensitive, recur and start showing resistance not only to the initial chemotherapeutic agent… (more)

Subjects/Keywords: drug-drug interaction; Efflux transporter inhibitors; Multi-drug resistance; pharmacokinetics; Tyrosine Kinase Inhibitors

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APA (6th Edition):

D'Cunha, R. R. (2018). Treatment strategies to reverse efflux transporter-mediated resistance to Tyrosine kinase inhibitors. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6563

Chicago Manual of Style (16th Edition):

D'Cunha, Ronilda Raymond. “Treatment strategies to reverse efflux transporter-mediated resistance to Tyrosine kinase inhibitors.” 2018. Doctoral Dissertation, University of Iowa. Accessed January 19, 2021. https://ir.uiowa.edu/etd/6563.

MLA Handbook (7th Edition):

D'Cunha, Ronilda Raymond. “Treatment strategies to reverse efflux transporter-mediated resistance to Tyrosine kinase inhibitors.” 2018. Web. 19 Jan 2021.

Vancouver:

D'Cunha RR. Treatment strategies to reverse efflux transporter-mediated resistance to Tyrosine kinase inhibitors. [Internet] [Doctoral dissertation]. University of Iowa; 2018. [cited 2021 Jan 19]. Available from: https://ir.uiowa.edu/etd/6563.

Council of Science Editors:

D'Cunha RR. Treatment strategies to reverse efflux transporter-mediated resistance to Tyrosine kinase inhibitors. [Doctoral Dissertation]. University of Iowa; 2018. Available from: https://ir.uiowa.edu/etd/6563


University of Edinburgh

11. Mehio, Wissam. Computational approaches for identifying inhibitors of protein interactions.

Degree: PhD, 2011, University of Edinburgh

 Inter-molecular interaction is at the heart of biological function. Proteins can interact with ligands, peptides, small molecules, and other proteins to serve their structural or… (more)

Subjects/Keywords: 572; inter-molecular interaction; computational drug discovery; protein interaction inhibitors; bioinformatics

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APA (6th Edition):

Mehio, W. (2011). Computational approaches for identifying inhibitors of protein interactions. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9503

Chicago Manual of Style (16th Edition):

Mehio, Wissam. “Computational approaches for identifying inhibitors of protein interactions.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed January 19, 2021. http://hdl.handle.net/1842/9503.

MLA Handbook (7th Edition):

Mehio, Wissam. “Computational approaches for identifying inhibitors of protein interactions.” 2011. Web. 19 Jan 2021.

Vancouver:

Mehio W. Computational approaches for identifying inhibitors of protein interactions. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1842/9503.

Council of Science Editors:

Mehio W. Computational approaches for identifying inhibitors of protein interactions. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/9503


Erasmus University Rotterdam

12. Hussaarts, Koen. Drug Interactions with Anti-Cancer Agents: A Pharmacokinetic and Pharmacodynamic Approach.

Degree: 2020, Erasmus University Rotterdam

This thesis describes different pharmacokinetic and pharmacodynamic drug interactions between anti-cancer agents and comedication or food. A great variety of drugs and interactions is described in this thesis.

Subjects/Keywords: Interactie; farmacokinetiek; farmacodynamiek; drug-drug interaction; food-drug interaction

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APA (6th Edition):

Hussaarts, K. (2020). Drug Interactions with Anti-Cancer Agents: A Pharmacokinetic and Pharmacodynamic Approach. (Doctoral Dissertation). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/132183

Chicago Manual of Style (16th Edition):

Hussaarts, Koen. “Drug Interactions with Anti-Cancer Agents: A Pharmacokinetic and Pharmacodynamic Approach.” 2020. Doctoral Dissertation, Erasmus University Rotterdam. Accessed January 19, 2021. http://hdl.handle.net/1765/132183.

MLA Handbook (7th Edition):

Hussaarts, Koen. “Drug Interactions with Anti-Cancer Agents: A Pharmacokinetic and Pharmacodynamic Approach.” 2020. Web. 19 Jan 2021.

Vancouver:

Hussaarts K. Drug Interactions with Anti-Cancer Agents: A Pharmacokinetic and Pharmacodynamic Approach. [Internet] [Doctoral dissertation]. Erasmus University Rotterdam; 2020. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1765/132183.

Council of Science Editors:

Hussaarts K. Drug Interactions with Anti-Cancer Agents: A Pharmacokinetic and Pharmacodynamic Approach. [Doctoral Dissertation]. Erasmus University Rotterdam; 2020. Available from: http://hdl.handle.net/1765/132183

13. 장, 철. Analyzing alert overrides reasons in the Drug Utilization Review system.

Degree: 2016, Ajou University

 All medical institutions in the country use a single Drug Utilization Review (DUR) System. Efficient DUR system operation requires continuous monitoring for alerts, especially ignored… (more)

Subjects/Keywords: Drug Utilization Review System; Drug-Drug Interaction; Alert override codes; Drug Utilization Review; 의약품사용평가시스템; 중복예외처방코드; 약물상호작용

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APA (6th Edition):

장, . (2016). Analyzing alert overrides reasons in the Drug Utilization Review system. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/18470 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021997

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):

장, 철. “Analyzing alert overrides reasons in the Drug Utilization Review system.” 2016. Thesis, Ajou University. Accessed January 19, 2021. http://repository.ajou.ac.kr/handle/201003/18470 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021997.

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

MLA Handbook (7th Edition):

장, 철. “Analyzing alert overrides reasons in the Drug Utilization Review system.” 2016. Web. 19 Jan 2021.

Vancouver:

장 . Analyzing alert overrides reasons in the Drug Utilization Review system. [Internet] [Thesis]. Ajou University; 2016. [cited 2021 Jan 19]. Available from: http://repository.ajou.ac.kr/handle/201003/18470 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021997.

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

Council of Science Editors:

장 . Analyzing alert overrides reasons in the Drug Utilization Review system. [Thesis]. Ajou University; 2016. Available from: http://repository.ajou.ac.kr/handle/201003/18470 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021997

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


Temple University

14. Youssef, Amir Samaan Bishara. Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions.

Degree: PhD, 2013, Temple University

Pharmaceutical Sciences

Gastroparesis is a disorder characterized by delayed gastric emptying due to chronic abnormal gastric motility. Prokinetic agents such as domperidone and metoclopramide are… (more)

Subjects/Keywords: Pharmaceutical sciences;

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APA (6th Edition):

Youssef, A. S. B. (2013). Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,231985

Chicago Manual of Style (16th Edition):

Youssef, Amir Samaan Bishara. “Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions.” 2013. Doctoral Dissertation, Temple University. Accessed January 19, 2021. http://digital.library.temple.edu/u?/p245801coll10,231985.

MLA Handbook (7th Edition):

Youssef, Amir Samaan Bishara. “Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions.” 2013. Web. 19 Jan 2021.

Vancouver:

Youssef ASB. Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2021 Jan 19]. Available from: http://digital.library.temple.edu/u?/p245801coll10,231985.

Council of Science Editors:

Youssef ASB. Improvement of Gastroparesis Management By Addressing Challenges in Drug Metabolism: Studies with Metabolite Identification, Reaction Phenotyping and In Vitro Drug-Drug Interactions. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,231985


Univerzitet u Beogradu

15. Stojković, Aleksandra M., 1984-. Biofarmaceutska karakterizacija interakcije ciprofloksacina i jona metala.

Degree: Farmaceutski fakultet, 2014, Univerzitet u Beogradu

Farmacija - Farmaceutska tehnologija / Pharmacy - Pharmaceutical technology

Biofarmaceutska karakterizacija podrazumeva sprovođenje odgovarajućih in vitro, in vivo i in silico ispitivanja s ciljem da… (more)

Subjects/Keywords: ciprofloxacin; dissolution; drug-drug interaction; in silico simulation; solid state characterisation; solubility

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APA (6th Edition):

Stojković, Aleksandra M., 1. (2014). Biofarmaceutska karakterizacija interakcije ciprofloksacina i jona metala. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:8491/bdef:Content/get

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):

Stojković, Aleksandra M., 1984-. “Biofarmaceutska karakterizacija interakcije ciprofloksacina i jona metala.” 2014. Thesis, Univerzitet u Beogradu. Accessed January 19, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:8491/bdef:Content/get.

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

MLA Handbook (7th Edition):

Stojković, Aleksandra M., 1984-. “Biofarmaceutska karakterizacija interakcije ciprofloksacina i jona metala.” 2014. Web. 19 Jan 2021.

Vancouver:

Stojković, Aleksandra M. 1. Biofarmaceutska karakterizacija interakcije ciprofloksacina i jona metala. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2021 Jan 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:8491/bdef:Content/get.

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

Council of Science Editors:

Stojković, Aleksandra M. 1. Biofarmaceutska karakterizacija interakcije ciprofloksacina i jona metala. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:8491/bdef:Content/get

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

16. Agbabiaka, Taofikat Bisola. Concurrent use of prescription drugs and herbal medicinal products among older adults.

Degree: PhD, 2020, University of Hertfordshire

 Background: Polypharmacy is a recognised patient safety risk, with older adults at greater risk due to co-morbidities and reduced clearance of drugs due to ageing.… (more)

Subjects/Keywords: Herbal medicine; Herbal; Herbal medicinal product; Older adult; Concurrent use; Dietary supplement; Herb-drug interaction; Supplement-drug interaction; Polypharmacy

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APA (6th Edition):

Agbabiaka, T. B. (2020). Concurrent use of prescription drugs and herbal medicinal products among older adults. (Doctoral Dissertation). University of Hertfordshire. Retrieved from http://hdl.handle.net/2299/22120

Chicago Manual of Style (16th Edition):

Agbabiaka, Taofikat Bisola. “Concurrent use of prescription drugs and herbal medicinal products among older adults.” 2020. Doctoral Dissertation, University of Hertfordshire. Accessed January 19, 2021. http://hdl.handle.net/2299/22120.

MLA Handbook (7th Edition):

Agbabiaka, Taofikat Bisola. “Concurrent use of prescription drugs and herbal medicinal products among older adults.” 2020. Web. 19 Jan 2021.

Vancouver:

Agbabiaka TB. Concurrent use of prescription drugs and herbal medicinal products among older adults. [Internet] [Doctoral dissertation]. University of Hertfordshire; 2020. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2299/22120.

Council of Science Editors:

Agbabiaka TB. Concurrent use of prescription drugs and herbal medicinal products among older adults. [Doctoral Dissertation]. University of Hertfordshire; 2020. Available from: http://hdl.handle.net/2299/22120

17. Rouhana, Jad. Etude et modulation des interactions protéine-protéine : l’activation de la petite protéine G Arf1 par son facteur d’échange Arno : Study and modulation of protein-protein interactions : Activation of the small G protein (Arf1) by its guanidine exchange factor (ARNO).

Degree: Docteur es, Biologie Santé, 2013, Université Montpellier I

Arf1 est une petite protéine G (pG), essentiellement impliquée dans le trafic vésiculaire. Arf1 oscille entre deux conformations, l'une active liée au GTP et l'autre… (more)

Subjects/Keywords: Fragment-based drug design; Spr; Interaction protéine-protéine; Fbdd; Spr; Protein-Protein Interaction; 577

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APA (6th Edition):

Rouhana, J. (2013). Etude et modulation des interactions protéine-protéine : l’activation de la petite protéine G Arf1 par son facteur d’échange Arno : Study and modulation of protein-protein interactions : Activation of the small G protein (Arf1) by its guanidine exchange factor (ARNO). (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2013MON13507

Chicago Manual of Style (16th Edition):

Rouhana, Jad. “Etude et modulation des interactions protéine-protéine : l’activation de la petite protéine G Arf1 par son facteur d’échange Arno : Study and modulation of protein-protein interactions : Activation of the small G protein (Arf1) by its guanidine exchange factor (ARNO).” 2013. Doctoral Dissertation, Université Montpellier I. Accessed January 19, 2021. http://www.theses.fr/2013MON13507.

MLA Handbook (7th Edition):

Rouhana, Jad. “Etude et modulation des interactions protéine-protéine : l’activation de la petite protéine G Arf1 par son facteur d’échange Arno : Study and modulation of protein-protein interactions : Activation of the small G protein (Arf1) by its guanidine exchange factor (ARNO).” 2013. Web. 19 Jan 2021.

Vancouver:

Rouhana J. Etude et modulation des interactions protéine-protéine : l’activation de la petite protéine G Arf1 par son facteur d’échange Arno : Study and modulation of protein-protein interactions : Activation of the small G protein (Arf1) by its guanidine exchange factor (ARNO). [Internet] [Doctoral dissertation]. Université Montpellier I; 2013. [cited 2021 Jan 19]. Available from: http://www.theses.fr/2013MON13507.

Council of Science Editors:

Rouhana J. Etude et modulation des interactions protéine-protéine : l’activation de la petite protéine G Arf1 par son facteur d’échange Arno : Study and modulation of protein-protein interactions : Activation of the small G protein (Arf1) by its guanidine exchange factor (ARNO). [Doctoral Dissertation]. Université Montpellier I; 2013. Available from: http://www.theses.fr/2013MON13507

18. Bhatta, Rabi Sankar. Bioavailability enhancement for a highly effective antihyperlipidemic agent 16 dehydropregnenalone and the evaluation of its drug drug interaction potential; -.

Degree: Drug Research, 2007, Jawaharlal Nehru University

None

References p.126, Figures p.iv, Tables p.vii

Advisors/Committee Members: Kumar, Girish.

Subjects/Keywords: Antihyperlipedemic; drug drug interaction; drug use; potential

Page 1

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APA (6th Edition):

Bhatta, R. S. (2007). Bioavailability enhancement for a highly effective antihyperlipidemic agent 16 dehydropregnenalone and the evaluation of its drug drug interaction potential; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/29562

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):

Bhatta, Rabi Sankar. “Bioavailability enhancement for a highly effective antihyperlipidemic agent 16 dehydropregnenalone and the evaluation of its drug drug interaction potential; -.” 2007. Thesis, Jawaharlal Nehru University. Accessed January 19, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/29562.

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

MLA Handbook (7th Edition):

Bhatta, Rabi Sankar. “Bioavailability enhancement for a highly effective antihyperlipidemic agent 16 dehydropregnenalone and the evaluation of its drug drug interaction potential; -.” 2007. Web. 19 Jan 2021.

Vancouver:

Bhatta RS. Bioavailability enhancement for a highly effective antihyperlipidemic agent 16 dehydropregnenalone and the evaluation of its drug drug interaction potential; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2007. [cited 2021 Jan 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29562.

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

Council of Science Editors:

Bhatta RS. Bioavailability enhancement for a highly effective antihyperlipidemic agent 16 dehydropregnenalone and the evaluation of its drug drug interaction potential; -. [Thesis]. Jawaharlal Nehru University; 2007. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/29562

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


University of Kansas

19. Logan, Randall. Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function.

Degree: PhD, Pharmaceutical Chemistry, 2013, University of Kansas

 From a clinical perspective, a drug's pharmacokinetic properties (e.g., the volume of distribution, clearance, and half-life) are vitally important as these parameters are used to… (more)

Subjects/Keywords: Pharmaceutical sciences; Cellular biology; Pharmacology; Cationic Amphiphilic Drugs; Drug distribution; Drug Drug interaction; intracellular distribution; Lysosome; Lysosomotropic

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APA (6th Edition):

Logan, R. (2013). Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21626

Chicago Manual of Style (16th Edition):

Logan, Randall. “Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function.” 2013. Doctoral Dissertation, University of Kansas. Accessed January 19, 2021. http://hdl.handle.net/1808/21626.

MLA Handbook (7th Edition):

Logan, Randall. “Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function.” 2013. Web. 19 Jan 2021.

Vancouver:

Logan R. Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1808/21626.

Council of Science Editors:

Logan R. Studies on the mechanisms and consequences of drug-induced perturbations of lysosomal structure and function. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/21626


Technical University of Lisbon

20. Varandas, Edna Soraia Gregório Ribeiro Varandas. Low-dose effects of Bisphenol A on human primary vascular endothelial cells and colon cancer cells.

Degree: 2014, Technical University of Lisbon

Doutoramento em Biologia - Instituto Superior de Agronomia

Bisphenol A (BPA) is an extensively utilized endocrine disruptor for which human exposure is considered generalized through… (more)

Subjects/Keywords: Bisphenol A (BPA); HUVEC; HT29; gene transcription; drug interaction

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APA (6th Edition):

Varandas, E. S. G. R. V. (2014). Low-dose effects of Bisphenol A on human primary vascular endothelial cells and colon cancer cells. (Thesis). Technical University of Lisbon. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/7338

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):

Varandas, Edna Soraia Gregório Ribeiro Varandas. “Low-dose effects of Bisphenol A on human primary vascular endothelial cells and colon cancer cells.” 2014. Thesis, Technical University of Lisbon. Accessed January 19, 2021. http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/7338.

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

MLA Handbook (7th Edition):

Varandas, Edna Soraia Gregório Ribeiro Varandas. “Low-dose effects of Bisphenol A on human primary vascular endothelial cells and colon cancer cells.” 2014. Web. 19 Jan 2021.

Vancouver:

Varandas ESGRV. Low-dose effects of Bisphenol A on human primary vascular endothelial cells and colon cancer cells. [Internet] [Thesis]. Technical University of Lisbon; 2014. [cited 2021 Jan 19]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/7338.

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

Council of Science Editors:

Varandas ESGRV. Low-dose effects of Bisphenol A on human primary vascular endothelial cells and colon cancer cells. [Thesis]. Technical University of Lisbon; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/7338

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

21. KURATA, Tomohiko. Characteristics of Pemetrexed Transport by Renal Basolateral Organic Anion Transporter hOAT3 : 腎側低膜のヒト有機アニオントランスポーターhOAT3によるペメトレキセドの輸送特性.

Degree: 博士(医学), 2017, Mie University / 三重大学

Purpose: Pemetrexed transport by human organic anion transporters, hOAT1 (SLC22A6) and hOAT3 (SLC22A8), were characterized in comparison with methotrexate. Methods: Accumulation of pemetrexed and methotrexate… (more)

Subjects/Keywords: pemetrexed; organic anion transporter; methotrexate; renal tubular secretion; drug interaction

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APA (6th Edition):

KURATA, T. (2017). Characteristics of Pemetrexed Transport by Renal Basolateral Organic Anion Transporter hOAT3 : 腎側低膜のヒト有機アニオントランスポーターhOAT3によるペメトレキセドの輸送特性. (Thesis). Mie University / 三重大学. Retrieved from http://hdl.handle.net/10076/00016982

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):

KURATA, Tomohiko. “Characteristics of Pemetrexed Transport by Renal Basolateral Organic Anion Transporter hOAT3 : 腎側低膜のヒト有機アニオントランスポーターhOAT3によるペメトレキセドの輸送特性.” 2017. Thesis, Mie University / 三重大学. Accessed January 19, 2021. http://hdl.handle.net/10076/00016982.

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

MLA Handbook (7th Edition):

KURATA, Tomohiko. “Characteristics of Pemetrexed Transport by Renal Basolateral Organic Anion Transporter hOAT3 : 腎側低膜のヒト有機アニオントランスポーターhOAT3によるペメトレキセドの輸送特性.” 2017. Web. 19 Jan 2021.

Vancouver:

KURATA T. Characteristics of Pemetrexed Transport by Renal Basolateral Organic Anion Transporter hOAT3 : 腎側低膜のヒト有機アニオントランスポーターhOAT3によるペメトレキセドの輸送特性. [Internet] [Thesis]. Mie University / 三重大学; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10076/00016982.

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

Council of Science Editors:

KURATA T. Characteristics of Pemetrexed Transport by Renal Basolateral Organic Anion Transporter hOAT3 : 腎側低膜のヒト有機アニオントランスポーターhOAT3によるペメトレキセドの輸送特性. [Thesis]. Mie University / 三重大学; 2017. Available from: http://hdl.handle.net/10076/00016982

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

22. Faria, Leila Márcia Pereira de. Interação medicamentosa: conhecimento de enfermeiros das unidades de terapia intensiva de três hospitais públicos de Goiânia - GO.

Degree: Mestrado, Enfermagem Fundamental, 2010, University of São Paulo

Atualmente, é uma preocupação a exposição dos pacientes de unidade de terapia intensiva (UTI) a situações da prática clínica que colocam suas vidas em risco.… (more)

Subjects/Keywords: drug Interaction; enfermagem; interação medicamentosa; nursing; patient safety; segurança do paciente

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APA (6th Edition):

Faria, L. M. P. d. (2010). Interação medicamentosa: conhecimento de enfermeiros das unidades de terapia intensiva de três hospitais públicos de Goiânia - GO. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/22/22132/tde-27092010-164203/ ;

Chicago Manual of Style (16th Edition):

Faria, Leila Márcia Pereira de. “Interação medicamentosa: conhecimento de enfermeiros das unidades de terapia intensiva de três hospitais públicos de Goiânia - GO.” 2010. Masters Thesis, University of São Paulo. Accessed January 19, 2021. http://www.teses.usp.br/teses/disponiveis/22/22132/tde-27092010-164203/ ;.

MLA Handbook (7th Edition):

Faria, Leila Márcia Pereira de. “Interação medicamentosa: conhecimento de enfermeiros das unidades de terapia intensiva de três hospitais públicos de Goiânia - GO.” 2010. Web. 19 Jan 2021.

Vancouver:

Faria LMPd. Interação medicamentosa: conhecimento de enfermeiros das unidades de terapia intensiva de três hospitais públicos de Goiânia - GO. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2021 Jan 19]. Available from: http://www.teses.usp.br/teses/disponiveis/22/22132/tde-27092010-164203/ ;.

Council of Science Editors:

Faria LMPd. Interação medicamentosa: conhecimento de enfermeiros das unidades de terapia intensiva de três hospitais públicos de Goiânia - GO. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/22/22132/tde-27092010-164203/ ;


Jawaharlal Nehru University

23. Jayaraman, G. Modulation of and anticancerdrug interaction patterns by radiation in simple cell systems; -.

Degree: Environment Science, 1984, Jawaharlal Nehru University

None

References p. 101-118

Advisors/Committee Members: Mookerjee, Anjali.

Subjects/Keywords: anticancer; carcinogenic; drug; interaction; patterns

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APA (6th Edition):

Jayaraman, G. (1984). Modulation of and anticancerdrug interaction patterns by radiation in simple cell systems; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/14353

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):

Jayaraman, G. “Modulation of and anticancerdrug interaction patterns by radiation in simple cell systems; -.” 1984. Thesis, Jawaharlal Nehru University. Accessed January 19, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/14353.

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

MLA Handbook (7th Edition):

Jayaraman, G. “Modulation of and anticancerdrug interaction patterns by radiation in simple cell systems; -.” 1984. Web. 19 Jan 2021.

Vancouver:

Jayaraman G. Modulation of and anticancerdrug interaction patterns by radiation in simple cell systems; -. [Internet] [Thesis]. Jawaharlal Nehru University; 1984. [cited 2021 Jan 19]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14353.

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

Council of Science Editors:

Jayaraman G. Modulation of and anticancerdrug interaction patterns by radiation in simple cell systems; -. [Thesis]. Jawaharlal Nehru University; 1984. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14353

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

24. Taniguchi, Masashi. Comparative in vitro studies of the metabolism of six 4-substituted methamphetamines and their inhibition of cytochrome P450 2D6 by GC-MS with trifluoroacetyl derivatization.

Degree: 博士(医学), 2017, Shiga University of Medical Science / 滋賀医科大学

学位論文題目 : Study on forensic drug testing of methamphetamines and related compounds by GC-MS with trifluoroacetyl derivatization.

Subjects/Keywords: Methamphetamine; Designer Drug; GC-MS; TFA Derivatization; Interaction; Metabolism

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APA (6th Edition):

Taniguchi, M. (2017). Comparative in vitro studies of the metabolism of six 4-substituted methamphetamines and their inhibition of cytochrome P450 2D6 by GC-MS with trifluoroacetyl derivatization. (Thesis). Shiga University of Medical Science / 滋賀医科大学. Retrieved from http://hdl.handle.net/10422/4200

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):

Taniguchi, Masashi. “Comparative in vitro studies of the metabolism of six 4-substituted methamphetamines and their inhibition of cytochrome P450 2D6 by GC-MS with trifluoroacetyl derivatization.” 2017. Thesis, Shiga University of Medical Science / 滋賀医科大学. Accessed January 19, 2021. http://hdl.handle.net/10422/4200.

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

MLA Handbook (7th Edition):

Taniguchi, Masashi. “Comparative in vitro studies of the metabolism of six 4-substituted methamphetamines and their inhibition of cytochrome P450 2D6 by GC-MS with trifluoroacetyl derivatization.” 2017. Web. 19 Jan 2021.

Vancouver:

Taniguchi M. Comparative in vitro studies of the metabolism of six 4-substituted methamphetamines and their inhibition of cytochrome P450 2D6 by GC-MS with trifluoroacetyl derivatization. [Internet] [Thesis]. Shiga University of Medical Science / 滋賀医科大学; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10422/4200.

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

Council of Science Editors:

Taniguchi M. Comparative in vitro studies of the metabolism of six 4-substituted methamphetamines and their inhibition of cytochrome P450 2D6 by GC-MS with trifluoroacetyl derivatization. [Thesis]. Shiga University of Medical Science / 滋賀医科大学; 2017. Available from: http://hdl.handle.net/10422/4200

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


Boston University

25. Zhong, Mengqi. Energetics and inhibition of the KEAP1/NRF2 protein-protein interaction interface.

Degree: PhD, Chemistry, 2017, Boston University

 Protein-protein interactions (PPI) represent a challenging target class in contemporary small molecule drug discovery. The difficulty arises because PPI sites are structurally and physicochemically different… (more)

Subjects/Keywords: Biochemistry; Binding hot spots; KEAP1/Nrf2; Drug discovery; Protein-protein interaction

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APA (6th Edition):

Zhong, M. (2017). Energetics and inhibition of the KEAP1/NRF2 protein-protein interaction interface. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/27178

Chicago Manual of Style (16th Edition):

Zhong, Mengqi. “Energetics and inhibition of the KEAP1/NRF2 protein-protein interaction interface.” 2017. Doctoral Dissertation, Boston University. Accessed January 19, 2021. http://hdl.handle.net/2144/27178.

MLA Handbook (7th Edition):

Zhong, Mengqi. “Energetics and inhibition of the KEAP1/NRF2 protein-protein interaction interface.” 2017. Web. 19 Jan 2021.

Vancouver:

Zhong M. Energetics and inhibition of the KEAP1/NRF2 protein-protein interaction interface. [Internet] [Doctoral dissertation]. Boston University; 2017. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2144/27178.

Council of Science Editors:

Zhong M. Energetics and inhibition of the KEAP1/NRF2 protein-protein interaction interface. [Doctoral Dissertation]. Boston University; 2017. Available from: http://hdl.handle.net/2144/27178


University of Toronto

26. Lam, Jessica Fung Chi. Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions.

Degree: PhD, 2014, University of Toronto

 Opioids are an important class of drugs used for the treatment of pain. The analgesic response and opioid-induced toxicity vary widely among patients. Of serious… (more)

Subjects/Keywords: Drug Interaction; Lactation; Neonate; Opioid; P-glycoprotein; Pharmacogenetics; 0419

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

APA (6th Edition):

Lam, J. F. C. (2014). Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68430

Chicago Manual of Style (16th Edition):

Lam, Jessica Fung Chi. “Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions.” 2014. Doctoral Dissertation, University of Toronto. Accessed January 19, 2021. http://hdl.handle.net/1807/68430.

MLA Handbook (7th Edition):

Lam, Jessica Fung Chi. “Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions.” 2014. Web. 19 Jan 2021.

Vancouver:

Lam JFC. Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1807/68430.

Council of Science Editors:

Lam JFC. Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68430

27. Tije, Albert Jan. Drug-interaction and Formulation Aspects of Taxanes in the Treatment of Cancer.

Degree: 2004, Erasmus University Medical Center

 markdownabstract__Abstract__ Over forty years ago, samples of the Taxus brevifolia, the pacific yew tree, were screened by the National Cancer Institute (NCI) for anticancer activity.… (more)

Subjects/Keywords: taxanes; drug-interaction; pharmacokinetics

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

APA (6th Edition):

Tije, A. J. (2004). Drug-interaction and Formulation Aspects of Taxanes in the Treatment of Cancer. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/51228

Chicago Manual of Style (16th Edition):

Tije, Albert Jan. “Drug-interaction and Formulation Aspects of Taxanes in the Treatment of Cancer.” 2004. Doctoral Dissertation, Erasmus University Medical Center. Accessed January 19, 2021. http://hdl.handle.net/1765/51228.

MLA Handbook (7th Edition):

Tije, Albert Jan. “Drug-interaction and Formulation Aspects of Taxanes in the Treatment of Cancer.” 2004. Web. 19 Jan 2021.

Vancouver:

Tije AJ. Drug-interaction and Formulation Aspects of Taxanes in the Treatment of Cancer. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2004. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1765/51228.

Council of Science Editors:

Tije AJ. Drug-interaction and Formulation Aspects of Taxanes in the Treatment of Cancer. [Doctoral Dissertation]. Erasmus University Medical Center; 2004. Available from: http://hdl.handle.net/1765/51228


University of Michigan

28. Epling, Daniel. Characterization of the Intestinal Permeability and Oral Absorption of Valacyclovir in Wildtype and huPepT1 Transgenic Mice.

Degree: PhD, Pharmaceutical Sciences, 2019, University of Michigan

 PepT1 (SLC15A1) is a transporter apically expressed along the epithelial cells of the gastrointestinal tract and is responsible for the absorption of di/tripeptides, ACE inhibitors,… (more)

Subjects/Keywords: Humanized PepT1; Intestinal Permeability; Pharmacokinetics; Oral Absorption; Valacyclovir; Drug-Drug Interaction; Pharmacy and Pharmacology; Health Sciences; Science

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APA (6th Edition):

Epling, D. (2019). Characterization of the Intestinal Permeability and Oral Absorption of Valacyclovir in Wildtype and huPepT1 Transgenic Mice. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/149998

Chicago Manual of Style (16th Edition):

Epling, Daniel. “Characterization of the Intestinal Permeability and Oral Absorption of Valacyclovir in Wildtype and huPepT1 Transgenic Mice.” 2019. Doctoral Dissertation, University of Michigan. Accessed January 19, 2021. http://hdl.handle.net/2027.42/149998.

MLA Handbook (7th Edition):

Epling, Daniel. “Characterization of the Intestinal Permeability and Oral Absorption of Valacyclovir in Wildtype and huPepT1 Transgenic Mice.” 2019. Web. 19 Jan 2021.

Vancouver:

Epling D. Characterization of the Intestinal Permeability and Oral Absorption of Valacyclovir in Wildtype and huPepT1 Transgenic Mice. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/2027.42/149998.

Council of Science Editors:

Epling D. Characterization of the Intestinal Permeability and Oral Absorption of Valacyclovir in Wildtype and huPepT1 Transgenic Mice. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/149998


University of Georgia

29. Li, Ting. Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat.

Degree: 2014, University of Georgia

 Physiologically-based pharmacokinetic (PBPK) modeling is a useful approach to investigate the absorption, distribution, metabolism and elimination (ADME) of a compound in animals as well as… (more)

Subjects/Keywords: physiologically-based pharmacokinetic model; dichloroacetic acid; nucleoside reverse transcriptase inhibitors; pregnancy; drug-drug interaction; suicide inhibition

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

APA (6th Edition):

Li, T. (2014). Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/24207

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, Ting. “Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat.” 2014. Thesis, University of Georgia. Accessed January 19, 2021. http://hdl.handle.net/10724/24207.

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

MLA Handbook (7th Edition):

Li, Ting. “Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat.” 2014. Web. 19 Jan 2021.

Vancouver:

Li T. Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10724/24207.

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

Council of Science Editors:

Li T. Physiologically-based pharmacokinetic modeling approach for drug disposition in human and pregnant rat. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/24207

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


University of Illinois – Chicago

30. Altaweel, Amjed. A Near Field Communication Detection System for Drug-Drug Interactions.

Degree: 2016, University of Illinois – Chicago

 One of the main problems that requires the increase of the worldwide awareness is the Adverse Drugs Reactions (ADRs) and more importantly their subset Drug-Drug… (more)

Subjects/Keywords: Adverse Drugs Reactions; Drug-Drug Interaction; NFC; unified identifier; Pharmacy End; Patient End; CAS Number; Arduino; Java; C/C++

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

APA (6th Edition):

Altaweel, A. (2016). A Near Field Communication Detection System for Drug-Drug Interactions. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/20906

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):

Altaweel, Amjed. “A Near Field Communication Detection System for Drug-Drug Interactions.” 2016. Thesis, University of Illinois – Chicago. Accessed January 19, 2021. http://hdl.handle.net/10027/20906.

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

MLA Handbook (7th Edition):

Altaweel, Amjed. “A Near Field Communication Detection System for Drug-Drug Interactions.” 2016. Web. 19 Jan 2021.

Vancouver:

Altaweel A. A Near Field Communication Detection System for Drug-Drug Interactions. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/10027/20906.

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

Council of Science Editors:

Altaweel A. A Near Field Communication Detection System for Drug-Drug Interactions. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/20906

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

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