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You searched for subject:(drug transporter). Showing records 1 – 30 of 77 total matches.

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Duke University

1. Johnson, Zachary Lee. Structural and Functional Studies of Concentrative Nucleoside Transporters .

Degree: 2015, Duke University

  Nucleoside transport into the cell plays a key role in providing building blocks for DNA and RNA synthesis, terminating adenosine signaling, and delivering nucleoside-analog… (more)

Subjects/Keywords: Biochemistry; Biophysics; concentrative nucleoside transporter; drug transporter; membrane protein; vcCNT

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APA (6th Edition):

Johnson, Z. L. (2015). Structural and Functional Studies of Concentrative Nucleoside Transporters . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9841

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):

Johnson, Zachary Lee. “Structural and Functional Studies of Concentrative Nucleoside Transporters .” 2015. Thesis, Duke University. Accessed April 13, 2021. http://hdl.handle.net/10161/9841.

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

MLA Handbook (7th Edition):

Johnson, Zachary Lee. “Structural and Functional Studies of Concentrative Nucleoside Transporters .” 2015. Web. 13 Apr 2021.

Vancouver:

Johnson ZL. Structural and Functional Studies of Concentrative Nucleoside Transporters . [Internet] [Thesis]. Duke University; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10161/9841.

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

Council of Science Editors:

Johnson ZL. Structural and Functional Studies of Concentrative Nucleoside Transporters . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/9841

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


The Ohio State University

2. Chen, Mingqing. Interactions between multi-kinase inhibitors and solute carrier transporters.

Degree: PhD, Pharmaceutical Sciences, 2020, The Ohio State University

 Tyrosine kinase inhibitors (TKIs) represent the largest class of anti-cancer drugs. By the end of 2019, there are a total of 46 granted FDA approval… (more)

Subjects/Keywords: Pharmaceuticals; drug transporter; DMPK; pharmacokinetics; drug-drug interactions

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APA (6th Edition):

Chen, M. (2020). Interactions between multi-kinase inhibitors and solute carrier transporters. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1585741410361704

Chicago Manual of Style (16th Edition):

Chen, Mingqing. “Interactions between multi-kinase inhibitors and solute carrier transporters.” 2020. Doctoral Dissertation, The Ohio State University. Accessed April 13, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1585741410361704.

MLA Handbook (7th Edition):

Chen, Mingqing. “Interactions between multi-kinase inhibitors and solute carrier transporters.” 2020. Web. 13 Apr 2021.

Vancouver:

Chen M. Interactions between multi-kinase inhibitors and solute carrier transporters. [Internet] [Doctoral dissertation]. The Ohio State University; 2020. [cited 2021 Apr 13]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1585741410361704.

Council of Science Editors:

Chen M. Interactions between multi-kinase inhibitors and solute carrier transporters. [Doctoral Dissertation]. The Ohio State University; 2020. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1585741410361704


Vanderbilt University

3. Ennis, Elizabeth Ann. Identification and Characterization of Novel Inhibitors of the Presynaptic, Hemicholinium-3-Sensitive Choline Transporter.

Degree: PhD, Pharmacology, 2016, Vanderbilt University

 Acetylcholine controls or modulates virtually every physiological process from the regulation of skeletal and smooth muscle contraction, to learning and memory (Sellers & Chess-Williams, 2012).… (more)

Subjects/Keywords: Choline; Drug discovery; anticholinergic; Transporter; Acetylcholine

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APA (6th Edition):

Ennis, E. A. (2016). Identification and Characterization of Novel Inhibitors of the Presynaptic, Hemicholinium-3-Sensitive Choline Transporter. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10650

Chicago Manual of Style (16th Edition):

Ennis, Elizabeth Ann. “Identification and Characterization of Novel Inhibitors of the Presynaptic, Hemicholinium-3-Sensitive Choline Transporter.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed April 13, 2021. http://hdl.handle.net/1803/10650.

MLA Handbook (7th Edition):

Ennis, Elizabeth Ann. “Identification and Characterization of Novel Inhibitors of the Presynaptic, Hemicholinium-3-Sensitive Choline Transporter.” 2016. Web. 13 Apr 2021.

Vancouver:

Ennis EA. Identification and Characterization of Novel Inhibitors of the Presynaptic, Hemicholinium-3-Sensitive Choline Transporter. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1803/10650.

Council of Science Editors:

Ennis EA. Identification and Characterization of Novel Inhibitors of the Presynaptic, Hemicholinium-3-Sensitive Choline Transporter. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/10650


Victoria University of Wellington

4. Simonson, Bridget. Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter.

Degree: 2011, Victoria University of Wellington

 Classic kappa opioid receptor (KOPr) agonists have shown anti-addictive properties in rat models of addiction (Heidbreder et al. 1998; Schenk et al. 1999; Sun et… (more)

Subjects/Keywords: Drug addiction; Kappa opioid receptor; Dopamine transporter

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APA (6th Edition):

Simonson, B. (2011). Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1676

Chicago Manual of Style (16th Edition):

Simonson, Bridget. “Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter.” 2011. Doctoral Dissertation, Victoria University of Wellington. Accessed April 13, 2021. http://hdl.handle.net/10063/1676.

MLA Handbook (7th Edition):

Simonson, Bridget. “Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter.” 2011. Web. 13 Apr 2021.

Vancouver:

Simonson B. Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2011. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10063/1676.

Council of Science Editors:

Simonson B. Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter. [Doctoral Dissertation]. Victoria University of Wellington; 2011. Available from: http://hdl.handle.net/10063/1676


University of California – San Francisco

5. Geier, Ethan George. Targeting Solute Carrier Transporters for Drug Delivery to the Central Nervous System.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2013, University of California – San Francisco

 The blood-brain barrier (BBB) is a major reason that approximately 95% of small molecule drugs developed to target the central nervous system (CNS) fail. Thus,… (more)

Subjects/Keywords: Pharmaceutical sciences; Pharmacology; Molecular biology; blood-brain barrier; cisplatin; drug delivery; drug transporter; large neutral amino acid transporter; solute carrier transporter

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APA (6th Edition):

Geier, E. G. (2013). Targeting Solute Carrier Transporters for Drug Delivery to the Central Nervous System. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/4qd5p455

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):

Geier, Ethan George. “Targeting Solute Carrier Transporters for Drug Delivery to the Central Nervous System.” 2013. Thesis, University of California – San Francisco. Accessed April 13, 2021. http://www.escholarship.org/uc/item/4qd5p455.

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

MLA Handbook (7th Edition):

Geier, Ethan George. “Targeting Solute Carrier Transporters for Drug Delivery to the Central Nervous System.” 2013. Web. 13 Apr 2021.

Vancouver:

Geier EG. Targeting Solute Carrier Transporters for Drug Delivery to the Central Nervous System. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/4qd5p455.

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

Council of Science Editors:

Geier EG. Targeting Solute Carrier Transporters for Drug Delivery to the Central Nervous System. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/4qd5p455

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


University of Guelph

6. Vitsupakorn, Danoo. Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter.

Degree: MS, Department of Molecular and Cellular Biology, 2014, University of Guelph

 The ABC multidrug transporter P-glycoprotein (Pgp, ABCB1) can transport structurally diverse substrates from the lipid bilayer. Pgp binds its substrates inside a large pocket with… (more)

Subjects/Keywords: membrane protein; ABC transporter; P-glycoprotein; drug binding; drug transport

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APA (6th Edition):

Vitsupakorn, D. (2014). Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398

Chicago Manual of Style (16th Edition):

Vitsupakorn, Danoo. “Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter.” 2014. Masters Thesis, University of Guelph. Accessed April 13, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398.

MLA Handbook (7th Edition):

Vitsupakorn, Danoo. “Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter.” 2014. Web. 13 Apr 2021.

Vancouver:

Vitsupakorn D. Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter. [Internet] [Masters thesis]. University of Guelph; 2014. [cited 2021 Apr 13]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398.

Council of Science Editors:

Vitsupakorn D. Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter. [Masters Thesis]. University of Guelph; 2014. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398


University of Arizona

7. Sandoval, Philip Joseph. Assessing Substrate-Dependence and Mechanism of Ligand Interaction with the Organic Cation Transporter, OCT2 .

Degree: 2018, University of Arizona

 Among its many functions, the kidney has a significant role in limiting the body’s exposure to potentially toxic xenobiotic compounds. One family of these compounds… (more)

Subjects/Keywords: Bayesian modeling; drug-drug interactions; OCT2; renal; transporter kinetics

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APA (6th Edition):

Sandoval, P. J. (2018). Assessing Substrate-Dependence and Mechanism of Ligand Interaction with the Organic Cation Transporter, OCT2 . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/628006

Chicago Manual of Style (16th Edition):

Sandoval, Philip Joseph. “Assessing Substrate-Dependence and Mechanism of Ligand Interaction with the Organic Cation Transporter, OCT2 .” 2018. Doctoral Dissertation, University of Arizona. Accessed April 13, 2021. http://hdl.handle.net/10150/628006.

MLA Handbook (7th Edition):

Sandoval, Philip Joseph. “Assessing Substrate-Dependence and Mechanism of Ligand Interaction with the Organic Cation Transporter, OCT2 .” 2018. Web. 13 Apr 2021.

Vancouver:

Sandoval PJ. Assessing Substrate-Dependence and Mechanism of Ligand Interaction with the Organic Cation Transporter, OCT2 . [Internet] [Doctoral dissertation]. University of Arizona; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10150/628006.

Council of Science Editors:

Sandoval PJ. Assessing Substrate-Dependence and Mechanism of Ligand Interaction with the Organic Cation Transporter, OCT2 . [Doctoral Dissertation]. University of Arizona; 2018. Available from: http://hdl.handle.net/10150/628006

8. 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 April 13, 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. 13 Apr 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 Apr 13]. 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 Kansas

9. Boxberger, Kelli Harmon. IDENTIFICATION OF ENDOGENOUS FUNCTION AND SUBSTRATE-DEPENDENT INTERACTIONS OF ORGANIC CATION TRANSPORTER 1.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2018, University of Kansas

 The human organic cation transporter 1 (hOCT1) is a polyspecific transporter, primarily expressed in the liver, which is known to interact with a large number… (more)

Subjects/Keywords: Pharmacology; computational modeling; drug disposition; drug-drug interactions; organic cation transporter; substrate-dependent interactions; transporters

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APA (6th Edition):

Boxberger, K. H. (2018). IDENTIFICATION OF ENDOGENOUS FUNCTION AND SUBSTRATE-DEPENDENT INTERACTIONS OF ORGANIC CATION TRANSPORTER 1. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27078

Chicago Manual of Style (16th Edition):

Boxberger, Kelli Harmon. “IDENTIFICATION OF ENDOGENOUS FUNCTION AND SUBSTRATE-DEPENDENT INTERACTIONS OF ORGANIC CATION TRANSPORTER 1.” 2018. Doctoral Dissertation, University of Kansas. Accessed April 13, 2021. http://hdl.handle.net/1808/27078.

MLA Handbook (7th Edition):

Boxberger, Kelli Harmon. “IDENTIFICATION OF ENDOGENOUS FUNCTION AND SUBSTRATE-DEPENDENT INTERACTIONS OF ORGANIC CATION TRANSPORTER 1.” 2018. Web. 13 Apr 2021.

Vancouver:

Boxberger KH. IDENTIFICATION OF ENDOGENOUS FUNCTION AND SUBSTRATE-DEPENDENT INTERACTIONS OF ORGANIC CATION TRANSPORTER 1. [Internet] [Doctoral dissertation]. University of Kansas; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1808/27078.

Council of Science Editors:

Boxberger KH. IDENTIFICATION OF ENDOGENOUS FUNCTION AND SUBSTRATE-DEPENDENT INTERACTIONS OF ORGANIC CATION TRANSPORTER 1. [Doctoral Dissertation]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/27078

10. 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 April 13, 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. 13 Apr 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 Apr 13]. 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


University of Toronto

11. Manan, Yaseen. Investigating the Structure of MacB, an ABC Transporter Protein.

Degree: 2015, University of Toronto

Despite the need to understand membrane proteins at the molecular level, fewer than 2% of the structures in the PDB are of membrane proteins. Detergents… (more)

Subjects/Keywords: ABC Transporter; Drug; Exporter; MacB; Membrane Proteins; X-Ray Crystallography; 0487

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APA (6th Edition):

Manan, Y. (2015). Investigating the Structure of MacB, an ABC Transporter Protein. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70462

Chicago Manual of Style (16th Edition):

Manan, Yaseen. “Investigating the Structure of MacB, an ABC Transporter Protein.” 2015. Masters Thesis, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/70462.

MLA Handbook (7th Edition):

Manan, Yaseen. “Investigating the Structure of MacB, an ABC Transporter Protein.” 2015. Web. 13 Apr 2021.

Vancouver:

Manan Y. Investigating the Structure of MacB, an ABC Transporter Protein. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/70462.

Council of Science Editors:

Manan Y. Investigating the Structure of MacB, an ABC Transporter Protein. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70462


University of California – San Francisco

12. Khuri, Natalia. COMPUTATIONAL PREDICTION OF MOLECULAR INTERACTIONS.

Degree: Biophysics, 2014, University of California – San Francisco

 Molecular interactions are of critical importance to all biological processes such as enzymatic reactions, transport, signaling, protein folding and aggregation, and macromolecular assembly. Proteins evolved… (more)

Subjects/Keywords: Biophysics; drug discovery; hemoglobin; simulation; structural biology; transporter

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APA (6th Edition):

Khuri, N. (2014). COMPUTATIONAL PREDICTION OF MOLECULAR INTERACTIONS. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/5v83806h

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):

Khuri, Natalia. “COMPUTATIONAL PREDICTION OF MOLECULAR INTERACTIONS.” 2014. Thesis, University of California – San Francisco. Accessed April 13, 2021. http://www.escholarship.org/uc/item/5v83806h.

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

MLA Handbook (7th Edition):

Khuri, Natalia. “COMPUTATIONAL PREDICTION OF MOLECULAR INTERACTIONS.” 2014. Web. 13 Apr 2021.

Vancouver:

Khuri N. COMPUTATIONAL PREDICTION OF MOLECULAR INTERACTIONS. [Internet] [Thesis]. University of California – San Francisco; 2014. [cited 2021 Apr 13]. Available from: http://www.escholarship.org/uc/item/5v83806h.

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

Council of Science Editors:

Khuri N. COMPUTATIONAL PREDICTION OF MOLECULAR INTERACTIONS. [Thesis]. University of California – San Francisco; 2014. Available from: http://www.escholarship.org/uc/item/5v83806h

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

13. Denecke, Shane. Probing insecticide biology using Drosophila melanogaster.

Degree: 2017, University of Melbourne

 Insecticides are often used to control insect pests, but resistance to these chemicals arises quickly, leading to agricultural losses and public health concerns. Understanding how… (more)

Subjects/Keywords: genetics; Drosophila; insecticide; drug resistance; P450; ABC transporter

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APA (6th Edition):

Denecke, S. (2017). Probing insecticide biology using Drosophila melanogaster. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/191214

Chicago Manual of Style (16th Edition):

Denecke, Shane. “Probing insecticide biology using Drosophila melanogaster.” 2017. Doctoral Dissertation, University of Melbourne. Accessed April 13, 2021. http://hdl.handle.net/11343/191214.

MLA Handbook (7th Edition):

Denecke, Shane. “Probing insecticide biology using Drosophila melanogaster.” 2017. Web. 13 Apr 2021.

Vancouver:

Denecke S. Probing insecticide biology using Drosophila melanogaster. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/11343/191214.

Council of Science Editors:

Denecke S. Probing insecticide biology using Drosophila melanogaster. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/191214


University of Arizona

14. Abdullahi, Wazir. Targeting Organic Anion Transporting Polypeptide 1A4 (Oatp1a4) for Effective Drug Delivery at the Blood-Brain Barrier .

Degree: 2019, University of Arizona

Drug delivery to the central nervous system (CNS) is greatly limited by the blood-brain barrier (BBB). Physical and biochemical properties of the BBB have rendered… (more)

Subjects/Keywords: Blood-brain barrier; Drug delivery; TGF-beta signaling; Transporter

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APA (6th Edition):

Abdullahi, W. (2019). Targeting Organic Anion Transporting Polypeptide 1A4 (Oatp1a4) for Effective Drug Delivery at the Blood-Brain Barrier . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/631886

Chicago Manual of Style (16th Edition):

Abdullahi, Wazir. “Targeting Organic Anion Transporting Polypeptide 1A4 (Oatp1a4) for Effective Drug Delivery at the Blood-Brain Barrier .” 2019. Doctoral Dissertation, University of Arizona. Accessed April 13, 2021. http://hdl.handle.net/10150/631886.

MLA Handbook (7th Edition):

Abdullahi, Wazir. “Targeting Organic Anion Transporting Polypeptide 1A4 (Oatp1a4) for Effective Drug Delivery at the Blood-Brain Barrier .” 2019. Web. 13 Apr 2021.

Vancouver:

Abdullahi W. Targeting Organic Anion Transporting Polypeptide 1A4 (Oatp1a4) for Effective Drug Delivery at the Blood-Brain Barrier . [Internet] [Doctoral dissertation]. University of Arizona; 2019. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10150/631886.

Council of Science Editors:

Abdullahi W. Targeting Organic Anion Transporting Polypeptide 1A4 (Oatp1a4) for Effective Drug Delivery at the Blood-Brain Barrier . [Doctoral Dissertation]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/631886


Duquesne University

15. Chaly, Anna. Computational Ligand-Based CNS Therapeutic Design: The Search for Novel-Scaffold Norepinephrine Transporter Inhibitors.

Degree: MS, Pharmacology, 2012, Duquesne University

 Monoamine transporter (MAT) proteins are responsible for regulating cellular signal transduction through control of neurotransmitter reuptake in the synapse, and are therefore relevant to diseases… (more)

Subjects/Keywords: Drug design; Ligand-Based; MOE; Monoamine transporters; Norepinephrine transporter; Pharmacophore model

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APA (6th Edition):

Chaly, A. (2012). Computational Ligand-Based CNS Therapeutic Design: The Search for Novel-Scaffold Norepinephrine Transporter Inhibitors. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/389

Chicago Manual of Style (16th Edition):

Chaly, Anna. “Computational Ligand-Based CNS Therapeutic Design: The Search for Novel-Scaffold Norepinephrine Transporter Inhibitors.” 2012. Masters Thesis, Duquesne University. Accessed April 13, 2021. https://dsc.duq.edu/etd/389.

MLA Handbook (7th Edition):

Chaly, Anna. “Computational Ligand-Based CNS Therapeutic Design: The Search for Novel-Scaffold Norepinephrine Transporter Inhibitors.” 2012. Web. 13 Apr 2021.

Vancouver:

Chaly A. Computational Ligand-Based CNS Therapeutic Design: The Search for Novel-Scaffold Norepinephrine Transporter Inhibitors. [Internet] [Masters thesis]. Duquesne University; 2012. [cited 2021 Apr 13]. Available from: https://dsc.duq.edu/etd/389.

Council of Science Editors:

Chaly A. Computational Ligand-Based CNS Therapeutic Design: The Search for Novel-Scaffold Norepinephrine Transporter Inhibitors. [Masters Thesis]. Duquesne University; 2012. Available from: https://dsc.duq.edu/etd/389

16. Cherukuri, Pavan Kumar. Design of Drug Nano-Carriers for Study of Multidrug Resistance in Single Live Cells.

Degree: PhD, Chemistry and Biochemistry, 2016, Old Dominion University

  Multidrug resistance (MDR) exists in both prokaryotic and eukaryotic cells. MDR is responsible for ineffective treatment of a wide range of diseases, such as… (more)

Subjects/Keywords: ABC transporter; Drug delivery; Multidrug resistances; Nano-carriers; Biochemistry; Biology; Nanotechnology

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APA (6th Edition):

Cherukuri, P. K. (2016). Design of Drug Nano-Carriers for Study of Multidrug Resistance in Single Live Cells. (Doctoral Dissertation). Old Dominion University. Retrieved from 9781369563856 ; https://digitalcommons.odu.edu/chemistry_etds/12

Chicago Manual of Style (16th Edition):

Cherukuri, Pavan Kumar. “Design of Drug Nano-Carriers for Study of Multidrug Resistance in Single Live Cells.” 2016. Doctoral Dissertation, Old Dominion University. Accessed April 13, 2021. 9781369563856 ; https://digitalcommons.odu.edu/chemistry_etds/12.

MLA Handbook (7th Edition):

Cherukuri, Pavan Kumar. “Design of Drug Nano-Carriers for Study of Multidrug Resistance in Single Live Cells.” 2016. Web. 13 Apr 2021.

Vancouver:

Cherukuri PK. Design of Drug Nano-Carriers for Study of Multidrug Resistance in Single Live Cells. [Internet] [Doctoral dissertation]. Old Dominion University; 2016. [cited 2021 Apr 13]. Available from: 9781369563856 ; https://digitalcommons.odu.edu/chemistry_etds/12.

Council of Science Editors:

Cherukuri PK. Design of Drug Nano-Carriers for Study of Multidrug Resistance in Single Live Cells. [Doctoral Dissertation]. Old Dominion University; 2016. Available from: 9781369563856 ; https://digitalcommons.odu.edu/chemistry_etds/12


Georgia State University

17. Zhang, Han. Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB.

Degree: PhD, Biology, 2013, Georgia State University

  Multi-drug resistance (MDR) has become a serious clinical problem for both cancer and infectious disease treatment. One of the leading causes of MDR is… (more)

Subjects/Keywords: Multi-drug resistance; C-terminal domain; ABC transporter; Membrane protein

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APA (6th Edition):

Zhang, H. (2013). Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/125

Chicago Manual of Style (16th Edition):

Zhang, Han. “Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB.” 2013. Doctoral Dissertation, Georgia State University. Accessed April 13, 2021. https://scholarworks.gsu.edu/biology_diss/125.

MLA Handbook (7th Edition):

Zhang, Han. “Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB.” 2013. Web. 13 Apr 2021.

Vancouver:

Zhang H. Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB. [Internet] [Doctoral dissertation]. Georgia State University; 2013. [cited 2021 Apr 13]. Available from: https://scholarworks.gsu.edu/biology_diss/125.

Council of Science Editors:

Zhang H. Mechanistic Studies Of Drug Resistance Conferred By An ABC Transporter DrrAB. [Doctoral Dissertation]. Georgia State University; 2013. Available from: https://scholarworks.gsu.edu/biology_diss/125


University of Toronto

18. Jahani Aval, Candice Marral. The Use of High-Dose Riboflavin to Limit Topotecan Efflux in Milk: A Proof-of-Principle Study in Mice and Cells.

Degree: 2018, University of Toronto

Various mechanisms mediate transport of compounds into milk throughout lactation. Breast cancer resistance protein (BCRP) is one of the apically expressed transport proteins in mammary… (more)

Subjects/Keywords: Breast cancer resistance protein; Drug transfer; Lactation; Riboflavin; Riboflavin transporter; Topotecan; 0419

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APA (6th Edition):

Jahani Aval, C. M. (2018). The Use of High-Dose Riboflavin to Limit Topotecan Efflux in Milk: A Proof-of-Principle Study in Mice and Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89572

Chicago Manual of Style (16th Edition):

Jahani Aval, Candice Marral. “The Use of High-Dose Riboflavin to Limit Topotecan Efflux in Milk: A Proof-of-Principle Study in Mice and Cells.” 2018. Masters Thesis, University of Toronto. Accessed April 13, 2021. http://hdl.handle.net/1807/89572.

MLA Handbook (7th Edition):

Jahani Aval, Candice Marral. “The Use of High-Dose Riboflavin to Limit Topotecan Efflux in Milk: A Proof-of-Principle Study in Mice and Cells.” 2018. Web. 13 Apr 2021.

Vancouver:

Jahani Aval CM. The Use of High-Dose Riboflavin to Limit Topotecan Efflux in Milk: A Proof-of-Principle Study in Mice and Cells. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1807/89572.

Council of Science Editors:

Jahani Aval CM. The Use of High-Dose Riboflavin to Limit Topotecan Efflux in Milk: A Proof-of-Principle Study in Mice and Cells. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89572


Virginia Commonwealth University

19. Mulgaonkar, Aditi. ASSESSMENT OF THE ROLE OF SOLUTE CARRIER DRUG TRANSPORTERS IN THE SYSTEMIC DISPOSITION OF FLUOROQUINOLONES: AN IN VITRO - IN VIVO COMPARISON.

Degree: PhD, Pharmaceutical Sciences, 2012, Virginia Commonwealth University

 Fluoroquinolones (FQ) are broad-spectrum charged antimicrobials exhibiting excellent tissue/fluid permeation. Thus, FQ disposition depends essentially on active transport and facilitative diffusion. Although most early transporter(more)

Subjects/Keywords: Transporters; Fluoroquinolones; Solute carrier drug transporter; SLC22; Medicine and Health Sciences; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Mulgaonkar, A. (2012). ASSESSMENT OF THE ROLE OF SOLUTE CARRIER DRUG TRANSPORTERS IN THE SYSTEMIC DISPOSITION OF FLUOROQUINOLONES: AN IN VITRO - IN VIVO COMPARISON. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/BY29-Q140 ; https://scholarscompass.vcu.edu/etd/2842

Chicago Manual of Style (16th Edition):

Mulgaonkar, Aditi. “ASSESSMENT OF THE ROLE OF SOLUTE CARRIER DRUG TRANSPORTERS IN THE SYSTEMIC DISPOSITION OF FLUOROQUINOLONES: AN IN VITRO - IN VIVO COMPARISON.” 2012. Doctoral Dissertation, Virginia Commonwealth University. Accessed April 13, 2021. https://doi.org/10.25772/BY29-Q140 ; https://scholarscompass.vcu.edu/etd/2842.

MLA Handbook (7th Edition):

Mulgaonkar, Aditi. “ASSESSMENT OF THE ROLE OF SOLUTE CARRIER DRUG TRANSPORTERS IN THE SYSTEMIC DISPOSITION OF FLUOROQUINOLONES: AN IN VITRO - IN VIVO COMPARISON.” 2012. Web. 13 Apr 2021.

Vancouver:

Mulgaonkar A. ASSESSMENT OF THE ROLE OF SOLUTE CARRIER DRUG TRANSPORTERS IN THE SYSTEMIC DISPOSITION OF FLUOROQUINOLONES: AN IN VITRO - IN VIVO COMPARISON. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2012. [cited 2021 Apr 13]. Available from: https://doi.org/10.25772/BY29-Q140 ; https://scholarscompass.vcu.edu/etd/2842.

Council of Science Editors:

Mulgaonkar A. ASSESSMENT OF THE ROLE OF SOLUTE CARRIER DRUG TRANSPORTERS IN THE SYSTEMIC DISPOSITION OF FLUOROQUINOLONES: AN IN VITRO - IN VIVO COMPARISON. [Doctoral Dissertation]. Virginia Commonwealth University; 2012. Available from: https://doi.org/10.25772/BY29-Q140 ; https://scholarscompass.vcu.edu/etd/2842


University of Western Ontario

20. DeGorter, Marianne K. Statin Transport by Hepatic Organic Anion-Transporting Polypeptides (OATPs).

Degree: 2012, University of Western Ontario

Drug transport proteins are important determinants of drug absorption, tissue accumulation, and elimination from the body, and there is growing appreciation for the contribution of… (more)

Subjects/Keywords: Organic anion-transporting polypeptides; pharmacogenetics; drug transporters; transporter knockout mice; statin transport; statin pharmacokinetics; Pharmacology

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APA (6th Edition):

DeGorter, M. K. (2012). Statin Transport by Hepatic Organic Anion-Transporting Polypeptides (OATPs). (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/691

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):

DeGorter, Marianne K. “Statin Transport by Hepatic Organic Anion-Transporting Polypeptides (OATPs).” 2012. Thesis, University of Western Ontario. Accessed April 13, 2021. https://ir.lib.uwo.ca/etd/691.

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

MLA Handbook (7th Edition):

DeGorter, Marianne K. “Statin Transport by Hepatic Organic Anion-Transporting Polypeptides (OATPs).” 2012. Web. 13 Apr 2021.

Vancouver:

DeGorter MK. Statin Transport by Hepatic Organic Anion-Transporting Polypeptides (OATPs). [Internet] [Thesis]. University of Western Ontario; 2012. [cited 2021 Apr 13]. Available from: https://ir.lib.uwo.ca/etd/691.

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

Council of Science Editors:

DeGorter MK. Statin Transport by Hepatic Organic Anion-Transporting Polypeptides (OATPs). [Thesis]. University of Western Ontario; 2012. Available from: https://ir.lib.uwo.ca/etd/691

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


University of Western Ontario

21. McLean, Cheynne C. Evaluation of Food Effects on the Oral Pharmacokinetics of Rosuvastatin.

Degree: 2016, University of Western Ontario

 Rosuvastatin is commonly prescribed for the treatment of hypercholesterolemia and exerts its effect through targeted accumulation in the liver. Current United States and Canadian dosing… (more)

Subjects/Keywords: rosuvastatin; HMG-CoA reductase inhibitors; oral pharmacokinetics; food effect; hepatic uptake transport; drug transporter pharmacogenetics

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APA (6th Edition):

McLean, C. C. (2016). Evaluation of Food Effects on the Oral Pharmacokinetics of Rosuvastatin. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/3774

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):

McLean, Cheynne C. “Evaluation of Food Effects on the Oral Pharmacokinetics of Rosuvastatin.” 2016. Thesis, University of Western Ontario. Accessed April 13, 2021. https://ir.lib.uwo.ca/etd/3774.

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

MLA Handbook (7th Edition):

McLean, Cheynne C. “Evaluation of Food Effects on the Oral Pharmacokinetics of Rosuvastatin.” 2016. Web. 13 Apr 2021.

Vancouver:

McLean CC. Evaluation of Food Effects on the Oral Pharmacokinetics of Rosuvastatin. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2021 Apr 13]. Available from: https://ir.lib.uwo.ca/etd/3774.

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

Council of Science Editors:

McLean CC. Evaluation of Food Effects on the Oral Pharmacokinetics of Rosuvastatin. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/3774

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


Duquesne University

22. Aggarwal, Shaili. Dopamine Transporter (DAT), Nicotinic Acetylcholine Receptor (nAChR), and Metabotropic Glutamate Receptor 2 (mGlu2) Irreversible Probes For Identifying Anti-Psychostimulant Therapeutics.

Degree: PhD, Medicinal Chemistry, 2014, Duquesne University

 Numerous in vitro and in vivo studies implicate that certain ligands that interact with DAT, nAChRs, and mGlu2 have tremendous potential as anti-addiction therapeutics. However,… (more)

Subjects/Keywords: Acetylcholine receptor; Chemical probes; Dopamine transporter; Drug addiction; Metabotropic glutamate receptor 2; Photoaffinity labeling

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APA (6th Edition):

Aggarwal, S. (2014). Dopamine Transporter (DAT), Nicotinic Acetylcholine Receptor (nAChR), and Metabotropic Glutamate Receptor 2 (mGlu2) Irreversible Probes For Identifying Anti-Psychostimulant Therapeutics. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/290

Chicago Manual of Style (16th Edition):

Aggarwal, Shaili. “Dopamine Transporter (DAT), Nicotinic Acetylcholine Receptor (nAChR), and Metabotropic Glutamate Receptor 2 (mGlu2) Irreversible Probes For Identifying Anti-Psychostimulant Therapeutics.” 2014. Doctoral Dissertation, Duquesne University. Accessed April 13, 2021. https://dsc.duq.edu/etd/290.

MLA Handbook (7th Edition):

Aggarwal, Shaili. “Dopamine Transporter (DAT), Nicotinic Acetylcholine Receptor (nAChR), and Metabotropic Glutamate Receptor 2 (mGlu2) Irreversible Probes For Identifying Anti-Psychostimulant Therapeutics.” 2014. Web. 13 Apr 2021.

Vancouver:

Aggarwal S. Dopamine Transporter (DAT), Nicotinic Acetylcholine Receptor (nAChR), and Metabotropic Glutamate Receptor 2 (mGlu2) Irreversible Probes For Identifying Anti-Psychostimulant Therapeutics. [Internet] [Doctoral dissertation]. Duquesne University; 2014. [cited 2021 Apr 13]. Available from: https://dsc.duq.edu/etd/290.

Council of Science Editors:

Aggarwal S. Dopamine Transporter (DAT), Nicotinic Acetylcholine Receptor (nAChR), and Metabotropic Glutamate Receptor 2 (mGlu2) Irreversible Probes For Identifying Anti-Psychostimulant Therapeutics. [Doctoral Dissertation]. Duquesne University; 2014. Available from: https://dsc.duq.edu/etd/290


Georgia State University

23. Rahman, Sadia J. Substrate Binding and Energy Transduction in a Multidrug Resistance ABC Transporter DrrAB.

Degree: PhD, Biology, 2018, Georgia State University

  Multidrug resistance (MDR) is a serious problem for treatment of cancers and infectious diseases. A leading cause of MDR is energy-dependent drug efflux by… (more)

Subjects/Keywords: ATP-binding cassette (ABC) transporter; multidrug resistance; intrinsic tryptophan fluorescence; energy transduction; drug binding; metagenomics

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APA (6th Edition):

Rahman, S. J. (2018). Substrate Binding and Energy Transduction in a Multidrug Resistance ABC Transporter DrrAB. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/210

Chicago Manual of Style (16th Edition):

Rahman, Sadia J. “Substrate Binding and Energy Transduction in a Multidrug Resistance ABC Transporter DrrAB.” 2018. Doctoral Dissertation, Georgia State University. Accessed April 13, 2021. https://scholarworks.gsu.edu/biology_diss/210.

MLA Handbook (7th Edition):

Rahman, Sadia J. “Substrate Binding and Energy Transduction in a Multidrug Resistance ABC Transporter DrrAB.” 2018. Web. 13 Apr 2021.

Vancouver:

Rahman SJ. Substrate Binding and Energy Transduction in a Multidrug Resistance ABC Transporter DrrAB. [Internet] [Doctoral dissertation]. Georgia State University; 2018. [cited 2021 Apr 13]. Available from: https://scholarworks.gsu.edu/biology_diss/210.

Council of Science Editors:

Rahman SJ. Substrate Binding and Energy Transduction in a Multidrug Resistance ABC Transporter DrrAB. [Doctoral Dissertation]. Georgia State University; 2018. Available from: https://scholarworks.gsu.edu/biology_diss/210


University of Alberta

24. Almukainzi, May Khalifah. The application of computer simulation to investigate drug absorption and bioavailability in disease states.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2015, University of Alberta

 Oral drug absorption relies mainly on the physicochemical drug properties and the interaction with the physiological environment of the body. These factors could be altered… (more)

Subjects/Keywords: MATE, OCT transporter; Top down approche ,bottom up approache; Metformin; Meloxicam, Ibuprofen; Gastroplus, Drug modelling,computer simulation, Drug bioavailability, Disease

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APA (6th Edition):

Almukainzi, M. K. (2015). The application of computer simulation to investigate drug absorption and bioavailability in disease states. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/n009w499v

Chicago Manual of Style (16th Edition):

Almukainzi, May Khalifah. “The application of computer simulation to investigate drug absorption and bioavailability in disease states.” 2015. Doctoral Dissertation, University of Alberta. Accessed April 13, 2021. https://era.library.ualberta.ca/files/n009w499v.

MLA Handbook (7th Edition):

Almukainzi, May Khalifah. “The application of computer simulation to investigate drug absorption and bioavailability in disease states.” 2015. Web. 13 Apr 2021.

Vancouver:

Almukainzi MK. The application of computer simulation to investigate drug absorption and bioavailability in disease states. [Internet] [Doctoral dissertation]. University of Alberta; 2015. [cited 2021 Apr 13]. Available from: https://era.library.ualberta.ca/files/n009w499v.

Council of Science Editors:

Almukainzi MK. The application of computer simulation to investigate drug absorption and bioavailability in disease states. [Doctoral Dissertation]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/n009w499v


University of Helsinki

25. Koskenkorva, Tiina. MDR1 as intestinal efflux protein : influence on drug absorption and drug-drug interactions (Literature review) : Interactions of aliskiren with MDR1 inhibitors in vitro and pharmacokinetic modeling of the influence of MDR1 on intestinal absorption (Experimental work): MDR1 effluksiproteiini ohutsuolessa : merkitys lääkeaineiden imeytymisessä ja lääke-lääke interaktioissa (kirjallisuuskatsaus) : Aliskireenin interaktio MDR1 inhibiittoreiden kanssa in vitro ja farmakokineettinen mallinnus MDR1 kuljetusproteiinin merkityksestä lääkeaineiden imeytymisessä (erikoistyö).

Degree: Farmaceutiska fakulteten, 2012, University of Helsinki

 Kuljetusproteiini- ja metaboliaentsyymivälitteisten lääke-lääke interaktioiden ennustaminen on tärkeä osa lääkkeen kehityskaarta. Kuitenkin tietämys kuljetusproteiinivälitteisten interaktioiden kliinisistä seurauksista on vielä rajallista ja lisää tutkimusta tarvitaan niiden… (more)

Subjects/Keywords: MDR1; transporter; drug-drug interaction; intestinal absorption; pharmacokinetic modeling; kuljetusproteiini; lääke-lääke interaktio; imeytyminen; farmakokineettinen mallitus; Biofarmaci; Biopharmacy; Biofarmasia

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APA (6th Edition):

Koskenkorva, T. (2012). MDR1 as intestinal efflux protein : influence on drug absorption and drug-drug interactions (Literature review) : Interactions of aliskiren with MDR1 inhibitors in vitro and pharmacokinetic modeling of the influence of MDR1 on intestinal absorption (Experimental work): MDR1 effluksiproteiini ohutsuolessa : merkitys lääkeaineiden imeytymisessä ja lääke-lääke interaktioissa (kirjallisuuskatsaus) : Aliskireenin interaktio MDR1 inhibiittoreiden kanssa in vitro ja farmakokineettinen mallinnus MDR1 kuljetusproteiinin merkityksestä lääkeaineiden imeytymisessä (erikoistyö). (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/32522

Chicago Manual of Style (16th Edition):

Koskenkorva, Tiina. “MDR1 as intestinal efflux protein : influence on drug absorption and drug-drug interactions (Literature review) : Interactions of aliskiren with MDR1 inhibitors in vitro and pharmacokinetic modeling of the influence of MDR1 on intestinal absorption (Experimental work): MDR1 effluksiproteiini ohutsuolessa : merkitys lääkeaineiden imeytymisessä ja lääke-lääke interaktioissa (kirjallisuuskatsaus) : Aliskireenin interaktio MDR1 inhibiittoreiden kanssa in vitro ja farmakokineettinen mallinnus MDR1 kuljetusproteiinin merkityksestä lääkeaineiden imeytymisessä (erikoistyö).” 2012. Masters Thesis, University of Helsinki. Accessed April 13, 2021. http://hdl.handle.net/10138/32522.

MLA Handbook (7th Edition):

Koskenkorva, Tiina. “MDR1 as intestinal efflux protein : influence on drug absorption and drug-drug interactions (Literature review) : Interactions of aliskiren with MDR1 inhibitors in vitro and pharmacokinetic modeling of the influence of MDR1 on intestinal absorption (Experimental work): MDR1 effluksiproteiini ohutsuolessa : merkitys lääkeaineiden imeytymisessä ja lääke-lääke interaktioissa (kirjallisuuskatsaus) : Aliskireenin interaktio MDR1 inhibiittoreiden kanssa in vitro ja farmakokineettinen mallinnus MDR1 kuljetusproteiinin merkityksestä lääkeaineiden imeytymisessä (erikoistyö).” 2012. Web. 13 Apr 2021.

Vancouver:

Koskenkorva T. MDR1 as intestinal efflux protein : influence on drug absorption and drug-drug interactions (Literature review) : Interactions of aliskiren with MDR1 inhibitors in vitro and pharmacokinetic modeling of the influence of MDR1 on intestinal absorption (Experimental work): MDR1 effluksiproteiini ohutsuolessa : merkitys lääkeaineiden imeytymisessä ja lääke-lääke interaktioissa (kirjallisuuskatsaus) : Aliskireenin interaktio MDR1 inhibiittoreiden kanssa in vitro ja farmakokineettinen mallinnus MDR1 kuljetusproteiinin merkityksestä lääkeaineiden imeytymisessä (erikoistyö). [Internet] [Masters thesis]. University of Helsinki; 2012. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10138/32522.

Council of Science Editors:

Koskenkorva T. MDR1 as intestinal efflux protein : influence on drug absorption and drug-drug interactions (Literature review) : Interactions of aliskiren with MDR1 inhibitors in vitro and pharmacokinetic modeling of the influence of MDR1 on intestinal absorption (Experimental work): MDR1 effluksiproteiini ohutsuolessa : merkitys lääkeaineiden imeytymisessä ja lääke-lääke interaktioissa (kirjallisuuskatsaus) : Aliskireenin interaktio MDR1 inhibiittoreiden kanssa in vitro ja farmakokineettinen mallinnus MDR1 kuljetusproteiinin merkityksestä lääkeaineiden imeytymisessä (erikoistyö). [Masters Thesis]. University of Helsinki; 2012. Available from: http://hdl.handle.net/10138/32522


Freie Universität Berlin

26. Preißner, Sarah. Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy.

Degree: 2015, Freie Universität Berlin

 More than half of the people aged 50 years or older are administered at least five drugs daily. The enzymes, which are responsible for the… (more)

Subjects/Keywords: personalized medicine; CYP; cytochrome P450; chemotherapy; transporter; drug-drug-interactions; drug enzyme interactions; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Preißner, S. (2015). Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10575

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):

Preißner, Sarah. “Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy.” 2015. Thesis, Freie Universität Berlin. Accessed April 13, 2021. https://refubium.fu-berlin.de/handle/fub188/10575.

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

MLA Handbook (7th Edition):

Preißner, Sarah. “Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy.” 2015. Web. 13 Apr 2021.

Vancouver:

Preißner S. Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2021 Apr 13]. Available from: https://refubium.fu-berlin.de/handle/fub188/10575.

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

Council of Science Editors:

Preißner S. Analysis of interactions and polymorphisms of xenobiotic enzymes for optimization of the medication and an exemplary application in polychemotherapy. [Thesis]. Freie Universität Berlin; 2015. Available from: https://refubium.fu-berlin.de/handle/fub188/10575

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

27. XIANG XIAOQIANG. Neuropharmacokinetic interaction between antiepileptic drugs.

Degree: 2006, National University of Singapore

Subjects/Keywords: antiepileptic drug; microdialysis; drug interaction; neuropharmacokinetics; drug transporter; blood brain barrier

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

APA (6th Edition):

XIAOQIANG, X. (2006). Neuropharmacokinetic interaction between antiepileptic drugs. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15445

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):

XIAOQIANG, XIANG. “Neuropharmacokinetic interaction between antiepileptic drugs.” 2006. Thesis, National University of Singapore. Accessed April 13, 2021. http://scholarbank.nus.edu.sg/handle/10635/15445.

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

MLA Handbook (7th Edition):

XIAOQIANG, XIANG. “Neuropharmacokinetic interaction between antiepileptic drugs.” 2006. Web. 13 Apr 2021.

Vancouver:

XIAOQIANG X. Neuropharmacokinetic interaction between antiepileptic drugs. [Internet] [Thesis]. National University of Singapore; 2006. [cited 2021 Apr 13]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15445.

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

Council of Science Editors:

XIAOQIANG X. Neuropharmacokinetic interaction between antiepileptic drugs. [Thesis]. National University of Singapore; 2006. Available from: http://scholarbank.nus.edu.sg/handle/10635/15445

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


University of Stirling

28. Heumann, Jan H. The potential role of ABC transporters as factors influencing drug susceptibility in the salmon louse, Lepeophtheirus salmonis (Kroyer, 1837).

Degree: PhD, 2014, University of Stirling

 Efficient control of sea lice is a major challenge for the sustainable production of farmed Atlantic salmon (Salmo salar (Linnaeus, 1758)). These marine ectoparasites feed… (more)

Subjects/Keywords: sea lice; salmon louse; Lepeophtheirus salmonis; L salmonis; Atlantic salmon; Salmo salar; emamectin benzoate; avermectin; drug resistance; drug susceptibility; ATP-binding cassette transporter; ABC transporter; bioassay; parasite; ectoparasite; copepod; Lepeophtheirus salmonis; Drug resistance in microorganisms; Fishes Diseases

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

APA (6th Edition):

Heumann, J. H. (2014). The potential role of ABC transporters as factors influencing drug susceptibility in the salmon louse, Lepeophtheirus salmonis (Kroyer, 1837). (Doctoral Dissertation). University of Stirling. Retrieved from http://hdl.handle.net/1893/21812

Chicago Manual of Style (16th Edition):

Heumann, Jan H. “The potential role of ABC transporters as factors influencing drug susceptibility in the salmon louse, Lepeophtheirus salmonis (Kroyer, 1837).” 2014. Doctoral Dissertation, University of Stirling. Accessed April 13, 2021. http://hdl.handle.net/1893/21812.

MLA Handbook (7th Edition):

Heumann, Jan H. “The potential role of ABC transporters as factors influencing drug susceptibility in the salmon louse, Lepeophtheirus salmonis (Kroyer, 1837).” 2014. Web. 13 Apr 2021.

Vancouver:

Heumann JH. The potential role of ABC transporters as factors influencing drug susceptibility in the salmon louse, Lepeophtheirus salmonis (Kroyer, 1837). [Internet] [Doctoral dissertation]. University of Stirling; 2014. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/1893/21812.

Council of Science Editors:

Heumann JH. The potential role of ABC transporters as factors influencing drug susceptibility in the salmon louse, Lepeophtheirus salmonis (Kroyer, 1837). [Doctoral Dissertation]. University of Stirling; 2014. Available from: http://hdl.handle.net/1893/21812

29. 髙原,典子. Drugs interacting with organic anion transporter-1 affect uptake of Tc-99m-mercaptoacetyl-triglycine (MAG3) in the human kidney: Therapeutic drug interaction in Tc-99m-MAG3 diagnosis of renal function and possible application of Tc-99m-MAG3 for drug development : 有機アニオントランスポーター(OAT1)と相互作用をもつ薬剤はヒト腎におけるTc-99m-Mercaptoacetyltriglycine(NAG3)の取り込みに影響する:治療的薬剤が有するMAG3腎機能診断への相互作用ならびに薬剤開発におけるMAG3利用の可能性について.

Degree: 博士(医学), University of Fukui / 福井大学

以下に掲載:Nuclear Medicine and Biology 40(5) pp.643-650 2013. Elsevier. 共著者:Noriko Takahara, Tuneo Saga, Masayuki Inubushi, Hiroyuki Kusuhara, Chie Seki, Sumito Ito, Nobuyuki Oyama, Osamu Yokoyama, Yuichi Sugiyama, Yasuhisa Fujibayashi

Subjects/Keywords: MAG3; Organic anion transporter; OAT1; Drug interaction; Kidney; Introduction

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

APA (6th Edition):

髙原,典子. (n.d.). Drugs interacting with organic anion transporter-1 affect uptake of Tc-99m-mercaptoacetyl-triglycine (MAG3) in the human kidney: Therapeutic drug interaction in Tc-99m-MAG3 diagnosis of renal function and possible application of Tc-99m-MAG3 for drug development : 有機アニオントランスポーター(OAT1)と相互作用をもつ薬剤はヒト腎におけるTc-99m-Mercaptoacetyltriglycine(NAG3)の取り込みに影響する:治療的薬剤が有するMAG3腎機能診断への相互作用ならびに薬剤開発におけるMAG3利用の可能性について. (Thesis). University of Fukui / 福井大学. Retrieved from http://hdl.handle.net/10098/8435

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

髙原,典子. “Drugs interacting with organic anion transporter-1 affect uptake of Tc-99m-mercaptoacetyl-triglycine (MAG3) in the human kidney: Therapeutic drug interaction in Tc-99m-MAG3 diagnosis of renal function and possible application of Tc-99m-MAG3 for drug development : 有機アニオントランスポーター(OAT1)と相互作用をもつ薬剤はヒト腎におけるTc-99m-Mercaptoacetyltriglycine(NAG3)の取り込みに影響する:治療的薬剤が有するMAG3腎機能診断への相互作用ならびに薬剤開発におけるMAG3利用の可能性について.” Thesis, University of Fukui / 福井大学. Accessed April 13, 2021. http://hdl.handle.net/10098/8435.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

髙原,典子. “Drugs interacting with organic anion transporter-1 affect uptake of Tc-99m-mercaptoacetyl-triglycine (MAG3) in the human kidney: Therapeutic drug interaction in Tc-99m-MAG3 diagnosis of renal function and possible application of Tc-99m-MAG3 for drug development : 有機アニオントランスポーター(OAT1)と相互作用をもつ薬剤はヒト腎におけるTc-99m-Mercaptoacetyltriglycine(NAG3)の取り込みに影響する:治療的薬剤が有するMAG3腎機能診断への相互作用ならびに薬剤開発におけるMAG3利用の可能性について.” Web. 13 Apr 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
No year of publication.

Vancouver:

髙原,典子. Drugs interacting with organic anion transporter-1 affect uptake of Tc-99m-mercaptoacetyl-triglycine (MAG3) in the human kidney: Therapeutic drug interaction in Tc-99m-MAG3 diagnosis of renal function and possible application of Tc-99m-MAG3 for drug development : 有機アニオントランスポーター(OAT1)と相互作用をもつ薬剤はヒト腎におけるTc-99m-Mercaptoacetyltriglycine(NAG3)の取り込みに影響する:治療的薬剤が有するMAG3腎機能診断への相互作用ならびに薬剤開発におけるMAG3利用の可能性について. [Internet] [Thesis]. University of Fukui / 福井大学; [cited 2021 Apr 13]. Available from: http://hdl.handle.net/10098/8435.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

髙原,典子. Drugs interacting with organic anion transporter-1 affect uptake of Tc-99m-mercaptoacetyl-triglycine (MAG3) in the human kidney: Therapeutic drug interaction in Tc-99m-MAG3 diagnosis of renal function and possible application of Tc-99m-MAG3 for drug development : 有機アニオントランスポーター(OAT1)と相互作用をもつ薬剤はヒト腎におけるTc-99m-Mercaptoacetyltriglycine(NAG3)の取り込みに影響する:治療的薬剤が有するMAG3腎機能診断への相互作用ならびに薬剤開発におけるMAG3利用の可能性について. [Thesis]. University of Fukui / 福井大学; Available from: http://hdl.handle.net/10098/8435

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Washington State University

30. [No author]. IN VITRO DRUG SUSCEPTIBILITY OF THEILERIA EQUI AND THE ROLE OF ABC TRANSPORTERS IN RESISTANCE TO IMIDOCARB DIPROPIONATE .

Degree: 2015, Washington State University

 The primary work presented involves evaluation of the apicomplexan hemoparasite Theileria equi for imidocarb dipropionate resistance, assessment of possible alternative treatment options, and investigation of… (more)

Subjects/Keywords: Veterinary science; Animal diseases; Pharmaceutical sciences; ABC transporter; bumped kinase inhibitor; drug resistance; equine; imidocarb; Theileria

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

APA (6th Edition):

author], [. (2015). IN VITRO DRUG SUSCEPTIBILITY OF THEILERIA EQUI AND THE ROLE OF ABC TRANSPORTERS IN RESISTANCE TO IMIDOCARB DIPROPIONATE . (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/6246

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

Chicago Manual of Style (16th Edition):

author], [No. “IN VITRO DRUG SUSCEPTIBILITY OF THEILERIA EQUI AND THE ROLE OF ABC TRANSPORTERS IN RESISTANCE TO IMIDOCARB DIPROPIONATE .” 2015. Thesis, Washington State University. Accessed April 13, 2021. http://hdl.handle.net/2376/6246.

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

MLA Handbook (7th Edition):

author], [No. “IN VITRO DRUG SUSCEPTIBILITY OF THEILERIA EQUI AND THE ROLE OF ABC TRANSPORTERS IN RESISTANCE TO IMIDOCARB DIPROPIONATE .” 2015. Web. 13 Apr 2021.

Vancouver:

author] [. IN VITRO DRUG SUSCEPTIBILITY OF THEILERIA EQUI AND THE ROLE OF ABC TRANSPORTERS IN RESISTANCE TO IMIDOCARB DIPROPIONATE . [Internet] [Thesis]. Washington State University; 2015. [cited 2021 Apr 13]. Available from: http://hdl.handle.net/2376/6246.

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

Council of Science Editors:

author] [. IN VITRO DRUG SUSCEPTIBILITY OF THEILERIA EQUI AND THE ROLE OF ABC TRANSPORTERS IN RESISTANCE TO IMIDOCARB DIPROPIONATE . [Thesis]. Washington State University; 2015. Available from: http://hdl.handle.net/2376/6246

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

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