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You searched for subject:(intracellular drug drug interaction). Showing records 1 – 30 of 32575 total matches.

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University of Kansas

1. 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 March 05, 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. 05 Mar 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 Mar 05]. 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


Vanderbilt University

2. Evans, Brian Connor. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.

Degree: MS, Biomedical Engineering, 2013, Vanderbilt University

 Peptide-based therapeutics have significant potential for use in a variety of clinical applications ranging from cancer therapy to promotion of cardiovascular health. However, the efficacy… (more)

Subjects/Keywords: intracellular; polyplex; Drug delivery; peptide

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APA (6th Edition):

Evans, B. C. (2013). Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11302

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):

Evans, Brian Connor. “Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.” 2013. Thesis, Vanderbilt University. Accessed March 05, 2021. http://hdl.handle.net/1803/11302.

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

MLA Handbook (7th Edition):

Evans, Brian Connor. “Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.” 2013. Web. 05 Mar 2021.

Vancouver:

Evans BC. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. [Internet] [Thesis]. Vanderbilt University; 2013. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1803/11302.

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

Council of Science Editors:

Evans BC. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. [Thesis]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/11302

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


University of Manchester

3. Al-Kotaji, Myasar. The multifunctional peptide, Tat-LK15 : a study of its cellular uptake and its potential use in drug delivery.

Degree: PhD, 2012, University of Manchester

 Cell penetrating peptides (CPPs) have been used in many areas of drug delivery for mediating the delivery of peptides, protein, DNA, siRNA and liposomes. Additionally… (more)

Subjects/Keywords: 615.1; CPPs; intracellular drug delivery

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APA (6th Edition):

Al-Kotaji, M. (2012). The multifunctional peptide, Tat-LK15 : a study of its cellular uptake and its potential use in drug delivery. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-multifunctional-peptide-tatlk15a-study-of-its-cellular-uptake-and-its-potential-use-in-drug-delivery(92514766-2626-4949-8e02-ca77dc88ff7b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566572

Chicago Manual of Style (16th Edition):

Al-Kotaji, Myasar. “The multifunctional peptide, Tat-LK15 : a study of its cellular uptake and its potential use in drug delivery.” 2012. Doctoral Dissertation, University of Manchester. Accessed March 05, 2021. https://www.research.manchester.ac.uk/portal/en/theses/the-multifunctional-peptide-tatlk15a-study-of-its-cellular-uptake-and-its-potential-use-in-drug-delivery(92514766-2626-4949-8e02-ca77dc88ff7b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566572.

MLA Handbook (7th Edition):

Al-Kotaji, Myasar. “The multifunctional peptide, Tat-LK15 : a study of its cellular uptake and its potential use in drug delivery.” 2012. Web. 05 Mar 2021.

Vancouver:

Al-Kotaji M. The multifunctional peptide, Tat-LK15 : a study of its cellular uptake and its potential use in drug delivery. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Mar 05]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-multifunctional-peptide-tatlk15a-study-of-its-cellular-uptake-and-its-potential-use-in-drug-delivery(92514766-2626-4949-8e02-ca77dc88ff7b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566572.

Council of Science Editors:

Al-Kotaji M. The multifunctional peptide, Tat-LK15 : a study of its cellular uptake and its potential use in drug delivery. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-multifunctional-peptide-tatlk15a-study-of-its-cellular-uptake-and-its-potential-use-in-drug-delivery(92514766-2626-4949-8e02-ca77dc88ff7b).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.566572


University of Manchester

4. Sullivan, Rebecca. Effect of glucuronides on metabolic enzymes and active hepatic uptake: in vitro assessment and prediction of drug-drug interaction risk.

Degree: 2016, University of Manchester

 The potential contribution of drug metabolites to drug-drug interactions (DDIs) is increasingly recognised. The latest FDA guidance recommends investigation of the effect of metabolites on… (more)

Subjects/Keywords: Glucuronide; Drug-drug interaction

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APA (6th Edition):

Sullivan, R. (2016). Effect of glucuronides on metabolic enzymes and active hepatic uptake: in vitro assessment and prediction of drug-drug interaction risk. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296143

Chicago Manual of Style (16th Edition):

Sullivan, Rebecca. “Effect of glucuronides on metabolic enzymes and active hepatic uptake: in vitro assessment and prediction of drug-drug interaction risk.” 2016. Doctoral Dissertation, University of Manchester. Accessed March 05, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296143.

MLA Handbook (7th Edition):

Sullivan, Rebecca. “Effect of glucuronides on metabolic enzymes and active hepatic uptake: in vitro assessment and prediction of drug-drug interaction risk.” 2016. Web. 05 Mar 2021.

Vancouver:

Sullivan R. Effect of glucuronides on metabolic enzymes and active hepatic uptake: in vitro assessment and prediction of drug-drug interaction risk. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Mar 05]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296143.

Council of Science Editors:

Sullivan R. Effect of glucuronides on metabolic enzymes and active hepatic uptake: in vitro assessment and prediction of drug-drug interaction risk. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:296143


University of KwaZulu-Natal

5. Khoza, Leon Joseph. Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain.

Degree: 2020, University of KwaZulu-Natal

 Mental disorders contribute to 13% of the global burden of disease. With major depressive disorder (MDD) expected to be the most significant contributor by 2030,… (more)

Subjects/Keywords: Ketamine.; Drug design.; Drug interaction.; Drug delivery.

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APA (6th Edition):

Khoza, L. J. (2020). Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/19171

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):

Khoza, Leon Joseph. “Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain.” 2020. Thesis, University of KwaZulu-Natal. Accessed March 05, 2021. https://researchspace.ukzn.ac.za/handle/10413/19171.

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

MLA Handbook (7th Edition):

Khoza, Leon Joseph. “Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain.” 2020. Web. 05 Mar 2021.

Vancouver:

Khoza LJ. Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain. [Internet] [Thesis]. University of KwaZulu-Natal; 2020. [cited 2021 Mar 05]. Available from: https://researchspace.ukzn.ac.za/handle/10413/19171.

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

Council of Science Editors:

Khoza LJ. Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain. [Thesis]. University of KwaZulu-Natal; 2020. Available from: https://researchspace.ukzn.ac.za/handle/10413/19171

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


Penn State University

6. 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 (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 March 05, 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. 05 Mar 2021.

Vancouver:

Davaasuren D. Analysis of Opioid Related Adverse Events and Signal Detection with Machine Learning. [Internet] [Thesis]. Penn State University; 2019. [cited 2021 Mar 05]. 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


Vanderbilt University

7. Kilchrist, Kameron V. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.

Degree: PhD, Biomedical Engineering, 2019, Vanderbilt University

 Since the FDA approved the first recombinant protein 37 years ago, drug developers have harnessed biologics to treat human disease. Despite tremendous progress in extracellular… (more)

Subjects/Keywords: intracellular drug delivery; drug delivery; endosome disruption; assay development

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APA (6th Edition):

Kilchrist, K. V. (2019). New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15474

Chicago Manual of Style (16th Edition):

Kilchrist, Kameron V. “New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed March 05, 2021. http://hdl.handle.net/1803/15474.

MLA Handbook (7th Edition):

Kilchrist, Kameron V. “New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.” 2019. Web. 05 Mar 2021.

Vancouver:

Kilchrist KV. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/1803/15474.

Council of Science Editors:

Kilchrist KV. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/15474


Universitat Politècnica de València

8. Giménez Morales, Cristina. Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents .

Degree: 2016, Universitat Politècnica de València

 [EN] The present PhD thesis, which is entitled "Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents" is… (more)

Subjects/Keywords: Mesoporous silica nanoparticles; Hybrid materials; Drug delivery system; Controlled drug delivery; Intracellular release

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APA (6th Edition):

Giménez Morales, C. (2016). Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents . (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/62822

Chicago Manual of Style (16th Edition):

Giménez Morales, Cristina. “Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents .” 2016. Doctoral Dissertation, Universitat Politècnica de València. Accessed March 05, 2021. http://hdl.handle.net/10251/62822.

MLA Handbook (7th Edition):

Giménez Morales, Cristina. “Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents .” 2016. Web. 05 Mar 2021.

Vancouver:

Giménez Morales C. Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents . [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2016. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/10251/62822.

Council of Science Editors:

Giménez Morales C. Design of new bio-gated nanodevices for advanced communication processes and targeted controlled release of therapeutic agents . [Doctoral Dissertation]. Universitat Politècnica de València; 2016. Available from: http://hdl.handle.net/10251/62822


Universitat Politècnica de València

9. De la Torre Paredes, Cristina. Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" .

Degree: 2018, Universitat Politècnica de València

 La presente tesis doctoral, titulada "Nanotecnología y química supramolecular en procesos de liberación controlada y reconocimiento molecular para aplicaciones biomédicas", se centra en dos temas… (more)

Subjects/Keywords: Mesoporous silica nanoparticles; Hybrid materials; Drug delivery system; Controlled drug delivery; Intracellular release

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APA (6th Edition):

De la Torre Paredes, C. (2018). Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" . (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/94043

Chicago Manual of Style (16th Edition):

De la Torre Paredes, Cristina. “Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" .” 2018. Doctoral Dissertation, Universitat Politècnica de València. Accessed March 05, 2021. http://hdl.handle.net/10251/94043.

MLA Handbook (7th Edition):

De la Torre Paredes, Cristina. “Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" .” 2018. Web. 05 Mar 2021.

Vancouver:

De la Torre Paredes C. Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" . [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2018. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/10251/94043.

Council of Science Editors:

De la Torre Paredes C. Nanotechnology and supramolecular chemistry in controlled release and molecular recognition proceses for biomedical applications" . [Doctoral Dissertation]. Universitat Politècnica de València; 2018. Available from: http://hdl.handle.net/10251/94043

10. Alkotaji, Myasar Ali. The multifunctional peptide, Tat-LK15:A study of its cellular uptake and its potential use in drug delivery.

Degree: 2012, University of Manchester

 AbstractCell penetrating peptides (CPPs) have been used in many areas of drug delivery for mediating the delivery of peptides, protein, DNA, siRNA and liposomes. Additionally… (more)

Subjects/Keywords: CPPs; intracellular drug delivery

…203 Figure ‎ 6-17 Intracellular distribution of doxorubicin in K562 and HT29 cell lines… …205 Figure ‎ 6-18 Intracellular distribution of doxorubicin in K562 and HT29 cell lines… …many areas of drug delivery for mediating the delivery of peptides, protein, DNA, siRNA and… …liposomes. Additionally they have shown an ability to overcome drug resistance in cells enhancing… …drug resistance of doxorubicin. Firstly Tat-LK15 peptide co-incubation with a model P-gp… 

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APA (6th Edition):

Alkotaji, M. A. (2012). The multifunctional peptide, Tat-LK15:A study of its cellular uptake and its potential use in drug delivery. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182371

Chicago Manual of Style (16th Edition):

Alkotaji, Myasar Ali. “The multifunctional peptide, Tat-LK15:A study of its cellular uptake and its potential use in drug delivery.” 2012. Doctoral Dissertation, University of Manchester. Accessed March 05, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182371.

MLA Handbook (7th Edition):

Alkotaji, Myasar Ali. “The multifunctional peptide, Tat-LK15:A study of its cellular uptake and its potential use in drug delivery.” 2012. Web. 05 Mar 2021.

Vancouver:

Alkotaji MA. The multifunctional peptide, Tat-LK15:A study of its cellular uptake and its potential use in drug delivery. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Mar 05]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182371.

Council of Science Editors:

Alkotaji MA. The multifunctional peptide, Tat-LK15:A study of its cellular uptake and its potential use in drug delivery. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:182371


Stellenbosch University

11. Visser, Johan Georg. Manipulation of macrophage phagocytosis - development of an endogenous delivery system.

Degree: PhD, Physiological Sciences, 2020, Stellenbosch University

ENGLISH ABSTRACT: The need to administer more potent antimicrobial drugs is supported by the ever-increasing incidence of multidrug resistance. Given the (necessary) higher toxicity of… (more)

Subjects/Keywords: Macrophages; Pharmaceutical biotechnology; Phagocytosis; Intracellular pathogen; UCTD; Drug delivery systems

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APA (6th Edition):

Visser, J. G. (2020). Manipulation of macrophage phagocytosis - development of an endogenous delivery system. (Doctoral Dissertation). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/107782

Chicago Manual of Style (16th Edition):

Visser, Johan Georg. “Manipulation of macrophage phagocytosis - development of an endogenous delivery system.” 2020. Doctoral Dissertation, Stellenbosch University. Accessed March 05, 2021. http://hdl.handle.net/10019.1/107782.

MLA Handbook (7th Edition):

Visser, Johan Georg. “Manipulation of macrophage phagocytosis - development of an endogenous delivery system.” 2020. Web. 05 Mar 2021.

Vancouver:

Visser JG. Manipulation of macrophage phagocytosis - development of an endogenous delivery system. [Internet] [Doctoral dissertation]. Stellenbosch University; 2020. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/10019.1/107782.

Council of Science Editors:

Visser JG. Manipulation of macrophage phagocytosis - development of an endogenous delivery system. [Doctoral Dissertation]. Stellenbosch University; 2020. Available from: http://hdl.handle.net/10019.1/107782

12. 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 March 05, 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. 05 Mar 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 Mar 05]. 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

13. 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 March 05, 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. 05 Mar 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 Mar 05]. 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

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

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 March 05, 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. 05 Mar 2021.

Vancouver:

Alabdulhafith M. NFC-Enabled Smartphone Application for Drug Interaction and Drug Allergy Detection. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 05]. 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

15. 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 March 05, 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. 05 Mar 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 Mar 05]. 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

16. 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 March 05, 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. 05 Mar 2021.

Vancouver:

Qiu X. Chemoprevention Study of Botanical Dietary Supplements by Mass Spectrometry. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2021 Mar 05]. 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

17. 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 March 05, 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. 05 Mar 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 Mar 05]. 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

18. 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 March 05, 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. 05 Mar 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 Mar 05]. 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

19. 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 March 05, 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. 05 Mar 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 Mar 05]. 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

20. 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 March 05, 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. 05 Mar 2021.

Vancouver:

장 . Analyzing alert overrides reasons in the Drug Utilization Review system. [Internet] [Thesis]. Ajou University; 2016. [cited 2021 Mar 05]. 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


University of Illinois – Urbana-Champaign

21. 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 March 05, 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. 05 Mar 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 Mar 05]. 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


Erasmus University Rotterdam

22. 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 March 05, 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. 05 Mar 2021.

Vancouver:

Hussaarts K. Drug Interactions with Anti-Cancer Agents: A Pharmacokinetic and Pharmacodynamic Approach. [Internet] [Doctoral dissertation]. Erasmus University Rotterdam; 2020. [cited 2021 Mar 05]. 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


Johannes Gutenberg Universität Mainz

23. Hofmann, Daniel. Drug delivery, entry and intracellular trafficking of polymeric nanoparticles.

Degree: 2014, Johannes Gutenberg Universität Mainz

 Polymere Nanopartikel sind kleine Teilchen, die vielseitige Einsatzmöglichkeiten für den Transport von Wirkstoffen bieten. Da Nanomaterialien in diesen biomedizinischen Anwendungen oft mit biologischen Systemen in… (more)

Subjects/Keywords: Wirkstofftransport, Nanopartikel, Endozytose, Intrazelluläre Transportwege; Drug delivery, nanoparticles, endocytosis, intracellular trafficking; Life sciences

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APA (6th Edition):

Hofmann, D. (2014). Drug delivery, entry and intracellular trafficking of polymeric nanoparticles. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2014/3915/

Chicago Manual of Style (16th Edition):

Hofmann, Daniel. “Drug delivery, entry and intracellular trafficking of polymeric nanoparticles.” 2014. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed March 05, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2014/3915/.

MLA Handbook (7th Edition):

Hofmann, Daniel. “Drug delivery, entry and intracellular trafficking of polymeric nanoparticles.” 2014. Web. 05 Mar 2021.

Vancouver:

Hofmann D. Drug delivery, entry and intracellular trafficking of polymeric nanoparticles. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2014. [cited 2021 Mar 05]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3915/.

Council of Science Editors:

Hofmann D. Drug delivery, entry and intracellular trafficking of polymeric nanoparticles. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2014. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3915/


Wayne State University

24. Wu, Kai. Exploration Of Cancer Proliferative Signaling In Chemotherapy Drug Resistance And Mdig-Induced Tumorigenesis.

Degree: PhD, Pharmaceutical Sciences, 2016, Wayne State University

  ABSTRACT EXPLORATION OF CANCER PROLIFERATIVE SIGNALING IN CHEMOTHERAPY DRUG RESISTANCE AND MDIG-INDUCED TUMORIGENESIS by KAI WU August 2016 Advisor: Dr. Fei Chen Major: Pharmaceutical… (more)

Subjects/Keywords: drug resistance; intracellular signaling; lung cancer; mdig; multiple myeloma; tumorigenesis; Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Wu, K. (2016). Exploration Of Cancer Proliferative Signaling In Chemotherapy Drug Resistance And Mdig-Induced Tumorigenesis. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1605

Chicago Manual of Style (16th Edition):

Wu, Kai. “Exploration Of Cancer Proliferative Signaling In Chemotherapy Drug Resistance And Mdig-Induced Tumorigenesis.” 2016. Doctoral Dissertation, Wayne State University. Accessed March 05, 2021. https://digitalcommons.wayne.edu/oa_dissertations/1605.

MLA Handbook (7th Edition):

Wu, Kai. “Exploration Of Cancer Proliferative Signaling In Chemotherapy Drug Resistance And Mdig-Induced Tumorigenesis.” 2016. Web. 05 Mar 2021.

Vancouver:

Wu K. Exploration Of Cancer Proliferative Signaling In Chemotherapy Drug Resistance And Mdig-Induced Tumorigenesis. [Internet] [Doctoral dissertation]. Wayne State University; 2016. [cited 2021 Mar 05]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1605.

Council of Science Editors:

Wu K. Exploration Of Cancer Proliferative Signaling In Chemotherapy Drug Resistance And Mdig-Induced Tumorigenesis. [Doctoral Dissertation]. Wayne State University; 2016. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1605


Addis Ababa University

25. Tadele, Markos. Identification of Anti-Leishmanial Leads from Open Access Pathogen Box .

Degree: 2019, Addis Ababa University

 Leishmaniasis is a vector-borne disease caused by an obligate intracellular protozoan of the genus Leishmania. The ranges of drugs available to treat this disease are… (more)

Subjects/Keywords: Leishmania donovani; Lishmania aethiopica; promastigotes; Intracellular Amastigotes; MMV Pathogen Box; drug screening; in vitro

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APA (6th Edition):

Tadele, M. (2019). Identification of Anti-Leishmanial Leads from Open Access Pathogen Box . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/handle/123456789/21139

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):

Tadele, Markos. “Identification of Anti-Leishmanial Leads from Open Access Pathogen Box .” 2019. Thesis, Addis Ababa University. Accessed March 05, 2021. http://etd.aau.edu.et/handle/123456789/21139.

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

MLA Handbook (7th Edition):

Tadele, Markos. “Identification of Anti-Leishmanial Leads from Open Access Pathogen Box .” 2019. Web. 05 Mar 2021.

Vancouver:

Tadele M. Identification of Anti-Leishmanial Leads from Open Access Pathogen Box . [Internet] [Thesis]. Addis Ababa University; 2019. [cited 2021 Mar 05]. Available from: http://etd.aau.edu.et/handle/123456789/21139.

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

Council of Science Editors:

Tadele M. Identification of Anti-Leishmanial Leads from Open Access Pathogen Box . [Thesis]. Addis Ababa University; 2019. Available from: http://etd.aau.edu.et/handle/123456789/21139

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


The Ohio State University

26. Zhou, Chenguang. NANOCARRIERS FOR THERAPEUTIC NUCLEIC ACID DELIVERY.

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

 The objective of this dissertation research is to develop nanocarrier (NC) systems for therapeutic nucleic acid delivery and to investigate the mechanism and kinetics of… (more)

Subjects/Keywords: Pharmaceuticals; nanoparticles; gene therapy; drug delivery; pharmacokinetics; siRNA; molecular beacon; intracellular trafficking

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APA (6th Edition):

Zhou, C. (2012). NANOCARRIERS FOR THERAPEUTIC NUCLEIC ACID DELIVERY. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1336584204

Chicago Manual of Style (16th Edition):

Zhou, Chenguang. “NANOCARRIERS FOR THERAPEUTIC NUCLEIC ACID DELIVERY.” 2012. Doctoral Dissertation, The Ohio State University. Accessed March 05, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1336584204.

MLA Handbook (7th Edition):

Zhou, Chenguang. “NANOCARRIERS FOR THERAPEUTIC NUCLEIC ACID DELIVERY.” 2012. Web. 05 Mar 2021.

Vancouver:

Zhou C. NANOCARRIERS FOR THERAPEUTIC NUCLEIC ACID DELIVERY. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2021 Mar 05]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1336584204.

Council of Science Editors:

Zhou C. NANOCARRIERS FOR THERAPEUTIC NUCLEIC ACID DELIVERY. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1336584204


University of Southern California

27. Bi, Lucun. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.

Degree: PhD, Pharmaceutical Sciences, 2008, University of Southern California

 High level of virologic failure was observed in HIV patients receiving combinations of tenofovir (TFV), lamivudine (3TC) combined with either abacavir (ABC) or didanosine (ddI).… (more)

Subjects/Keywords: nucleoside analog; NRTI; intracellular drug-drug interaction; efflux transporters; MRP2; MRP4; cellular adaptive response; ddNTP; TFV; ABC; ddI; endogenous nucleotide pools; PNP

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APA (6th Edition):

Bi, L. (2008). Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609

Chicago Manual of Style (16th Edition):

Bi, Lucun. “Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609.

MLA Handbook (7th Edition):

Bi, Lucun. “Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.” 2008. Web. 05 Mar 2021.

Vancouver:

Bi L. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609.

Council of Science Editors:

Bi L. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609


University of Nairobi

28. Maganya, Seth J. Evaluation of potential drug-drug interactions among mentally ill patients admitted at mathari mental hospital .

Degree: 2014, University of Nairobi

 Background: Mental health refers to a wider range of activities directly or indirectly related to the mental well-being. Multiple social, psychological and biological factors determine… (more)

Subjects/Keywords: Drug-drug interactions

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APA (6th Edition):

Maganya, S. J. (2014). Evaluation of potential drug-drug interactions among mentally ill patients admitted at mathari mental hospital . (Thesis). University of Nairobi. Retrieved from http://hdl.handle.net/11295/95111

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):

Maganya, Seth J. “Evaluation of potential drug-drug interactions among mentally ill patients admitted at mathari mental hospital .” 2014. Thesis, University of Nairobi. Accessed March 05, 2021. http://hdl.handle.net/11295/95111.

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

MLA Handbook (7th Edition):

Maganya, Seth J. “Evaluation of potential drug-drug interactions among mentally ill patients admitted at mathari mental hospital .” 2014. Web. 05 Mar 2021.

Vancouver:

Maganya SJ. Evaluation of potential drug-drug interactions among mentally ill patients admitted at mathari mental hospital . [Internet] [Thesis]. University of Nairobi; 2014. [cited 2021 Mar 05]. Available from: http://hdl.handle.net/11295/95111.

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

Council of Science Editors:

Maganya SJ. Evaluation of potential drug-drug interactions among mentally ill patients admitted at mathari mental hospital . [Thesis]. University of Nairobi; 2014. Available from: http://hdl.handle.net/11295/95111

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

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

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 March 05, 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. 05 Mar 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 Mar 05]. 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


Temple University

30. 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 March 05, 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. 05 Mar 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 Mar 05]. 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

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