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You searched for subject:(P Glycoprotein). Showing records 1 – 30 of 162 total matches.

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Drexel University

1. Meng, Zhou. Identification of System Independent and Dependent Parameters for Reliable in vitro-in vivo Extrapolation of P-glycoprotein using a Mass Action Kinetic Model.

Degree: 2015, Drexel University

 <p>The purpose of this work is to investigate the best kinetic parameters for incorporation into mechanistic PBPK model for P-gp using a mass action kinetic… (more)

Subjects/Keywords: Biology; P-glycoprotein

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APA (6th Edition):

Meng, Z. (2015). Identification of System Independent and Dependent Parameters for Reliable in vitro-in vivo Extrapolation of P-glycoprotein using a Mass Action Kinetic Model. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7214

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):

Meng, Zhou. “Identification of System Independent and Dependent Parameters for Reliable in vitro-in vivo Extrapolation of P-glycoprotein using a Mass Action Kinetic Model.” 2015. Thesis, Drexel University. Accessed November 22, 2019. http://hdl.handle.net/1860/idea:7214.

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

MLA Handbook (7th Edition):

Meng, Zhou. “Identification of System Independent and Dependent Parameters for Reliable in vitro-in vivo Extrapolation of P-glycoprotein using a Mass Action Kinetic Model.” 2015. Web. 22 Nov 2019.

Vancouver:

Meng Z. Identification of System Independent and Dependent Parameters for Reliable in vitro-in vivo Extrapolation of P-glycoprotein using a Mass Action Kinetic Model. [Internet] [Thesis]. Drexel University; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1860/idea:7214.

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

Council of Science Editors:

Meng Z. Identification of System Independent and Dependent Parameters for Reliable in vitro-in vivo Extrapolation of P-glycoprotein using a Mass Action Kinetic Model. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:7214

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


University of Texas Medical Branch – Galveston

2. [No author]. Placental P-glycoprotein: Role in disposition of medications administered during pregnancy .

Degree: 2010, University of Texas Medical Branch – Galveston

 The placenta supports fetal growth and regulates the bio-distribution of substances between the maternal and fetal circulation. Active efflux transporters in the placental apical membrane… (more)

Subjects/Keywords: placenta; p-glycoprotein; MDR1

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APA (6th Edition):

author], [. (2010). Placental P-glycoprotein: Role in disposition of medications administered during pregnancy . (Thesis). University of Texas Medical Branch – Galveston. Retrieved from http://hdl.handle.net/2152.3/142

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. “Placental P-glycoprotein: Role in disposition of medications administered during pregnancy .” 2010. Thesis, University of Texas Medical Branch – Galveston. Accessed November 22, 2019. http://hdl.handle.net/2152.3/142.

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. “Placental P-glycoprotein: Role in disposition of medications administered during pregnancy .” 2010. Web. 22 Nov 2019.

Vancouver:

author] [. Placental P-glycoprotein: Role in disposition of medications administered during pregnancy . [Internet] [Thesis]. University of Texas Medical Branch – Galveston; 2010. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2152.3/142.

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

Council of Science Editors:

author] [. Placental P-glycoprotein: Role in disposition of medications administered during pregnancy . [Thesis]. University of Texas Medical Branch – Galveston; 2010. Available from: http://hdl.handle.net/2152.3/142

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


University of Sydney

3. Seebacher, Nicole Aveline. Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones .

Degree: 2015, University of Sydney

 Multi-drug resistance (MDR) is the principal mechanism by which many cancers develop resistance to chemotherapy drugs. It is the major factor responsible for the failure… (more)

Subjects/Keywords: P-glycoprotein; Multidrug resistance; Resistance; Chemotherapy

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APA (6th Edition):

Seebacher, N. A. (2015). Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/13847

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):

Seebacher, Nicole Aveline. “Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones .” 2015. Thesis, University of Sydney. Accessed November 22, 2019. http://hdl.handle.net/2123/13847.

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

MLA Handbook (7th Edition):

Seebacher, Nicole Aveline. “Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones .” 2015. Web. 22 Nov 2019.

Vancouver:

Seebacher NA. Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones . [Internet] [Thesis]. University of Sydney; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2123/13847.

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

Council of Science Editors:

Seebacher NA. Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones . [Thesis]. University of Sydney; 2015. Available from: http://hdl.handle.net/2123/13847

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


Oregon State University

4. Fan, Ying. Effect of pharmaceuticals and natural products on multidrug resistance mediated transport in Caco-2 and MDCKII-MDR1 drug transport models.

Degree: PhD, Pharmacy, 2007, Oregon State University

 This thesis details my investigation of some pharmaceuticals and natural products on the transport of drugs which are substrates of P-glycoprotein (P-gp), such as cyclosporin… (more)

Subjects/Keywords: Pharmaceuticals; P-glycoprotein

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APA (6th Edition):

Fan, Y. (2007). Effect of pharmaceuticals and natural products on multidrug resistance mediated transport in Caco-2 and MDCKII-MDR1 drug transport models. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/7575

Chicago Manual of Style (16th Edition):

Fan, Ying. “Effect of pharmaceuticals and natural products on multidrug resistance mediated transport in Caco-2 and MDCKII-MDR1 drug transport models.” 2007. Doctoral Dissertation, Oregon State University. Accessed November 22, 2019. http://hdl.handle.net/1957/7575.

MLA Handbook (7th Edition):

Fan, Ying. “Effect of pharmaceuticals and natural products on multidrug resistance mediated transport in Caco-2 and MDCKII-MDR1 drug transport models.” 2007. Web. 22 Nov 2019.

Vancouver:

Fan Y. Effect of pharmaceuticals and natural products on multidrug resistance mediated transport in Caco-2 and MDCKII-MDR1 drug transport models. [Internet] [Doctoral dissertation]. Oregon State University; 2007. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1957/7575.

Council of Science Editors:

Fan Y. Effect of pharmaceuticals and natural products on multidrug resistance mediated transport in Caco-2 and MDCKII-MDR1 drug transport models. [Doctoral Dissertation]. Oregon State University; 2007. Available from: http://hdl.handle.net/1957/7575


University of Houston

5. Yang, Zhen 1982-. Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches.

Degree: Pharmacological and Pharmaceutical Sciences, Department of, 2012, University of Houston

 Objective: The overall goal is to determine the major factors limiting oral bioavailability of ginsenosides and utilizing the knowledge gained to increase the oral bioavailability… (more)

Subjects/Keywords: Bioavailability; Pharmacokinetics; Ginsenosides; P-glycoprotein; Transporter

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APA (6th Edition):

Yang, Z. 1. (2012). Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/1648

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

Chicago Manual of Style (16th Edition):

Yang, Zhen 1982-. “Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches.” 2012. Thesis, University of Houston. Accessed November 22, 2019. http://hdl.handle.net/10657/1648.

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

MLA Handbook (7th Edition):

Yang, Zhen 1982-. “Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches.” 2012. Web. 22 Nov 2019.

Vancouver:

Yang Z1. Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches. [Internet] [Thesis]. University of Houston; 2012. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10657/1648.

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

Council of Science Editors:

Yang Z1. Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches. [Thesis]. University of Houston; 2012. Available from: http://hdl.handle.net/10657/1648

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

6. Strycharz, Joseph P. Polygenic Resistance In The Highly DDT-resistant 91-r Strain Of Drosophila Melanogaster Involves Decreased Penetration, Increased Metabolism And Direct Excretion Of Ddt.

Degree: MS, Animal Science, 2010, University of Massachusetts

 Resistance to dichlorodiphenyltrichloroethane (DDT) in the 91-R strain of Drosophila melanogaster is extremely high compared to the susceptible Canton-S strain (>1500 times). Oxidative detoxification is… (more)

Subjects/Keywords: DDT; Drosophila; Resistance; Metabolism; P-glycoprotein; Biotechnology

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APA (6th Edition):

Strycharz, J. P. (2010). Polygenic Resistance In The Highly DDT-resistant 91-r Strain Of Drosophila Melanogaster Involves Decreased Penetration, Increased Metabolism And Direct Excretion Of Ddt. (Masters Thesis). University of Massachusetts. Retrieved from https://scholarworks.umass.edu/theses/424

Chicago Manual of Style (16th Edition):

Strycharz, Joseph P. “Polygenic Resistance In The Highly DDT-resistant 91-r Strain Of Drosophila Melanogaster Involves Decreased Penetration, Increased Metabolism And Direct Excretion Of Ddt.” 2010. Masters Thesis, University of Massachusetts. Accessed November 22, 2019. https://scholarworks.umass.edu/theses/424.

MLA Handbook (7th Edition):

Strycharz, Joseph P. “Polygenic Resistance In The Highly DDT-resistant 91-r Strain Of Drosophila Melanogaster Involves Decreased Penetration, Increased Metabolism And Direct Excretion Of Ddt.” 2010. Web. 22 Nov 2019.

Vancouver:

Strycharz JP. Polygenic Resistance In The Highly DDT-resistant 91-r Strain Of Drosophila Melanogaster Involves Decreased Penetration, Increased Metabolism And Direct Excretion Of Ddt. [Internet] [Masters thesis]. University of Massachusetts; 2010. [cited 2019 Nov 22]. Available from: https://scholarworks.umass.edu/theses/424.

Council of Science Editors:

Strycharz JP. Polygenic Resistance In The Highly DDT-resistant 91-r Strain Of Drosophila Melanogaster Involves Decreased Penetration, Increased Metabolism And Direct Excretion Of Ddt. [Masters Thesis]. University of Massachusetts; 2010. Available from: https://scholarworks.umass.edu/theses/424


University of Arizona

7. Schaefer, Charles. Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure .

Degree: 2017, University of Arizona

 The rates of opioid prescription and use have continued to increase over the last few decades. In turn, a greater number of patients suffer from… (more)

Subjects/Keywords: bbb; blood-brain barrier; opioid epidemic; p-glycoprotein; pgp; p-gp

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APA (6th Edition):

Schaefer, C. (2017). Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/624091

Chicago Manual of Style (16th Edition):

Schaefer, Charles. “Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure .” 2017. Masters Thesis, University of Arizona. Accessed November 22, 2019. http://hdl.handle.net/10150/624091.

MLA Handbook (7th Edition):

Schaefer, Charles. “Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure .” 2017. Web. 22 Nov 2019.

Vancouver:

Schaefer C. Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure . [Internet] [Masters thesis]. University of Arizona; 2017. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10150/624091.

Council of Science Editors:

Schaefer C. Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure . [Masters Thesis]. University of Arizona; 2017. Available from: http://hdl.handle.net/10150/624091


Universitat Pompeu Fabra

8. Rodríguez Torrecillas, Ivan, 1979-. Molecular basis to human P-glycoprotein reversion.

Degree: Departament de Ciències Experimentals i de la Salut, 2015, Universitat Pompeu Fabra

 Los transportadores ABC (ATP binding cassette), encargados de transportar un amplio espectro de moléculas a través de la bicapa lipídica, pueden estar asociados con diversas… (more)

Subjects/Keywords: Bioquimica; Diseño con ayuda de ordenador; P-glycoprotein; Transportadores ABC; Sesquiterpenes; Biochemistry; Computer aided drug design; P-glycoprotein; ABC transporters; 577

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APA (6th Edition):

Rodríguez Torrecillas, Ivan, 1. (2015). Molecular basis to human P-glycoprotein reversion. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/586099

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):

Rodríguez Torrecillas, Ivan, 1979-. “Molecular basis to human P-glycoprotein reversion.” 2015. Thesis, Universitat Pompeu Fabra. Accessed November 22, 2019. http://hdl.handle.net/10803/586099.

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

MLA Handbook (7th Edition):

Rodríguez Torrecillas, Ivan, 1979-. “Molecular basis to human P-glycoprotein reversion.” 2015. Web. 22 Nov 2019.

Vancouver:

Rodríguez Torrecillas, Ivan 1. Molecular basis to human P-glycoprotein reversion. [Internet] [Thesis]. Universitat Pompeu Fabra; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10803/586099.

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

Council of Science Editors:

Rodríguez Torrecillas, Ivan 1. Molecular basis to human P-glycoprotein reversion. [Thesis]. Universitat Pompeu Fabra; 2015. Available from: http://hdl.handle.net/10803/586099

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

9. Morgan, Alex D. Quantitative Estimation of P-glycorptein-Mediated Drug Transport by Mechanistically Modeled Intrinsic Clearance.

Degree: 2015, University of Western Ontario

P-glycoprotein (P-gp/ABCB1) is an important efflux drug transporter affecting the disposition of 50% of marketed drugs. Cell monolayer permeability assays are the gold standard for… (more)

Subjects/Keywords: P-glycoprotein; P-gp; modeled intrinsic clearance; apparent permeability; efflux ratio; monolayer permeability assay; Pharmacology

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APA (6th Edition):

Morgan, A. D. (2015). Quantitative Estimation of P-glycorptein-Mediated Drug Transport by Mechanistically Modeled Intrinsic Clearance. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2961

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):

Morgan, Alex D. “Quantitative Estimation of P-glycorptein-Mediated Drug Transport by Mechanistically Modeled Intrinsic Clearance.” 2015. Thesis, University of Western Ontario. Accessed November 22, 2019. https://ir.lib.uwo.ca/etd/2961.

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

MLA Handbook (7th Edition):

Morgan, Alex D. “Quantitative Estimation of P-glycorptein-Mediated Drug Transport by Mechanistically Modeled Intrinsic Clearance.” 2015. Web. 22 Nov 2019.

Vancouver:

Morgan AD. Quantitative Estimation of P-glycorptein-Mediated Drug Transport by Mechanistically Modeled Intrinsic Clearance. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2019 Nov 22]. Available from: https://ir.lib.uwo.ca/etd/2961.

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

Council of Science Editors:

Morgan AD. Quantitative Estimation of P-glycorptein-Mediated Drug Transport by Mechanistically Modeled Intrinsic Clearance. [Thesis]. University of Western Ontario; 2015. Available from: https://ir.lib.uwo.ca/etd/2961

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

10. Alame, Ghina. Étude de la réversion du phénotype de Multi Drug Resistance (MDR) par de nouveaux dérivés stéroïdiens, in vitro sur des lignées cellulaires humaines et murines résistantes et in vivo par xénogreffes : Reversion of MultiDrugResistance (MDR) phenotype by new steroids derivatives, in vitro (resistant human tumor cell line) and in vivo (xenografts models).

Degree: Docteur es, Biologie cellulaire et moléculaire, 2009, Université Claude Bernard – Lyon I

 <p>La chimiorésistance des cancers est caractérisée par une résistance pléïotropique à de multiples médicaments. Ce mécanisme est en partie causé par la surexpression des transporteurs… (more)

Subjects/Keywords: Phénotype MDR; Glycoprotéine-P; Stéroïdes; Cancer; Progestérone; MDR phenotype; P-glycoprotein; Steroid; Cancer; Progesterone; 616.994

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APA (6th Edition):

Alame, G. (2009). Étude de la réversion du phénotype de Multi Drug Resistance (MDR) par de nouveaux dérivés stéroïdiens, in vitro sur des lignées cellulaires humaines et murines résistantes et in vivo par xénogreffes : Reversion of MultiDrugResistance (MDR) phenotype by new steroids derivatives, in vitro (resistant human tumor cell line) and in vivo (xenografts models). (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2009LYO10223

Chicago Manual of Style (16th Edition):

Alame, Ghina. “Étude de la réversion du phénotype de Multi Drug Resistance (MDR) par de nouveaux dérivés stéroïdiens, in vitro sur des lignées cellulaires humaines et murines résistantes et in vivo par xénogreffes : Reversion of MultiDrugResistance (MDR) phenotype by new steroids derivatives, in vitro (resistant human tumor cell line) and in vivo (xenografts models).” 2009. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed November 22, 2019. http://www.theses.fr/2009LYO10223.

MLA Handbook (7th Edition):

Alame, Ghina. “Étude de la réversion du phénotype de Multi Drug Resistance (MDR) par de nouveaux dérivés stéroïdiens, in vitro sur des lignées cellulaires humaines et murines résistantes et in vivo par xénogreffes : Reversion of MultiDrugResistance (MDR) phenotype by new steroids derivatives, in vitro (resistant human tumor cell line) and in vivo (xenografts models).” 2009. Web. 22 Nov 2019.

Vancouver:

Alame G. Étude de la réversion du phénotype de Multi Drug Resistance (MDR) par de nouveaux dérivés stéroïdiens, in vitro sur des lignées cellulaires humaines et murines résistantes et in vivo par xénogreffes : Reversion of MultiDrugResistance (MDR) phenotype by new steroids derivatives, in vitro (resistant human tumor cell line) and in vivo (xenografts models). [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2009. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2009LYO10223.

Council of Science Editors:

Alame G. Étude de la réversion du phénotype de Multi Drug Resistance (MDR) par de nouveaux dérivés stéroïdiens, in vitro sur des lignées cellulaires humaines et murines résistantes et in vivo par xénogreffes : Reversion of MultiDrugResistance (MDR) phenotype by new steroids derivatives, in vitro (resistant human tumor cell line) and in vivo (xenografts models). [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2009. Available from: http://www.theses.fr/2009LYO10223

11. Issouf, Mohamed. Etude du rôle des P-glycoprotéines dans le dialogue moléculaire entre Haemonchus contortus et Heligmosomoides polygyrus bakeri et leurs hôtes : Role of P-Glycoproteins in molecular cross talk between Haemonchus contortus and heligmosomoides polygyrus bakeri and their hosts.

Degree: Docteur es, Sciences de la Vie et de la Santé, 2013, Université François-Rabelais de Tours

 <p>Le parasitisme est un des principaux problèmes dans les élevages des ruminants. Les nématodes parasites du tractus digestif des ovins et caprins sont responsables d’importantes… (more)

Subjects/Keywords: Nématode; Éosinophile; P-glycoprotéine; Cholestérol; Interaction hôte-parasite; Nematode; Eosinophil; P-glycoprotein; Cholesterol; Immune evasion

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APA (6th Edition):

Issouf, M. (2013). Etude du rôle des P-glycoprotéines dans le dialogue moléculaire entre Haemonchus contortus et Heligmosomoides polygyrus bakeri et leurs hôtes : Role of P-Glycoproteins in molecular cross talk between Haemonchus contortus and heligmosomoides polygyrus bakeri and their hosts. (Doctoral Dissertation). Université François-Rabelais de Tours. Retrieved from http://www.theses.fr/2013TOUR4035

Chicago Manual of Style (16th Edition):

Issouf, Mohamed. “Etude du rôle des P-glycoprotéines dans le dialogue moléculaire entre Haemonchus contortus et Heligmosomoides polygyrus bakeri et leurs hôtes : Role of P-Glycoproteins in molecular cross talk between Haemonchus contortus and heligmosomoides polygyrus bakeri and their hosts.” 2013. Doctoral Dissertation, Université François-Rabelais de Tours. Accessed November 22, 2019. http://www.theses.fr/2013TOUR4035.

MLA Handbook (7th Edition):

Issouf, Mohamed. “Etude du rôle des P-glycoprotéines dans le dialogue moléculaire entre Haemonchus contortus et Heligmosomoides polygyrus bakeri et leurs hôtes : Role of P-Glycoproteins in molecular cross talk between Haemonchus contortus and heligmosomoides polygyrus bakeri and their hosts.” 2013. Web. 22 Nov 2019.

Vancouver:

Issouf M. Etude du rôle des P-glycoprotéines dans le dialogue moléculaire entre Haemonchus contortus et Heligmosomoides polygyrus bakeri et leurs hôtes : Role of P-Glycoproteins in molecular cross talk between Haemonchus contortus and heligmosomoides polygyrus bakeri and their hosts. [Internet] [Doctoral dissertation]. Université François-Rabelais de Tours; 2013. [cited 2019 Nov 22]. Available from: http://www.theses.fr/2013TOUR4035.

Council of Science Editors:

Issouf M. Etude du rôle des P-glycoprotéines dans le dialogue moléculaire entre Haemonchus contortus et Heligmosomoides polygyrus bakeri et leurs hôtes : Role of P-Glycoproteins in molecular cross talk between Haemonchus contortus and heligmosomoides polygyrus bakeri and their hosts. [Doctoral Dissertation]. Université François-Rabelais de Tours; 2013. Available from: http://www.theses.fr/2013TOUR4035


University of Oxford

12. Pluchino, Kristen Marie. Generation of chimeric P-glycoprotein for functional and structural investigations.

Degree: PhD, 2015, University of Oxford

 A major challenge in cancer treatment is acquired or intrinsic multidrug resistance (MDR) to chemotherapeutics. A notorious mediator of MDR is P-glycoprotein (P-gp, ABCB1), product… (more)

Subjects/Keywords: Oncology; Medical Sciences; Multidrug resistance; Crystallography; Membrane proteins; P-glycoprotein; chimera

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APA (6th Edition):

Pluchino, K. M. (2015). Generation of chimeric P-glycoprotein for functional and structural investigations. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:4f5c9dcc-401c-4123-9b2f-c5d17e0d7bc2 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647697

Chicago Manual of Style (16th Edition):

Pluchino, Kristen Marie. “Generation of chimeric P-glycoprotein for functional and structural investigations.” 2015. Doctoral Dissertation, University of Oxford. Accessed November 22, 2019. http://ora.ox.ac.uk/objects/uuid:4f5c9dcc-401c-4123-9b2f-c5d17e0d7bc2 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647697.

MLA Handbook (7th Edition):

Pluchino, Kristen Marie. “Generation of chimeric P-glycoprotein for functional and structural investigations.” 2015. Web. 22 Nov 2019.

Vancouver:

Pluchino KM. Generation of chimeric P-glycoprotein for functional and structural investigations. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2019 Nov 22]. Available from: http://ora.ox.ac.uk/objects/uuid:4f5c9dcc-401c-4123-9b2f-c5d17e0d7bc2 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647697.

Council of Science Editors:

Pluchino KM. Generation of chimeric P-glycoprotein for functional and structural investigations. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:4f5c9dcc-401c-4123-9b2f-c5d17e0d7bc2 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.647697


Dalhousie University

13. Wang, Yan. Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid.

Degree: MS, College of Pharmacy, 2014, Dalhousie University

 <p>Master of Science Thesis p><p>Background: Inflammation-induced alterations in drug disposition during inflammatory conditions such as infection and surgery are common and may lead to altered… (more)

Subjects/Keywords: Blood-brain barrier; cardiopulmonary bypass; p-glycoprotein; morphine

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APA (6th Edition):

Wang, Y. (2014). Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/54084

Chicago Manual of Style (16th Edition):

Wang, Yan. “Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid.” 2014. Masters Thesis, Dalhousie University. Accessed November 22, 2019. http://hdl.handle.net/10222/54084.

MLA Handbook (7th Edition):

Wang, Yan. “Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid.” 2014. Web. 22 Nov 2019.

Vancouver:

Wang Y. Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10222/54084.

Council of Science Editors:

Wang Y. Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid. [Masters Thesis]. Dalhousie University; 2014. Available from: http://hdl.handle.net/10222/54084


Texas A&M University

14. Garretson, Pamela Donn. Role of P-glycoprotein in Haemonchus contortus anthelmintic resistance.

Degree: 2009, Texas A&M University

 The gastrointestinal parasite, Haemonchus contortus, is of major concern in the sheep and goat industry as well as in zoological settings. Over the years this… (more)

Subjects/Keywords: Anthelmintic resistance; Goats; Haemonchus contortus; Haemonchosis; P-glycoprotein; Sheep

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APA (6th Edition):

Garretson, P. D. (2009). Role of P-glycoprotein in Haemonchus contortus anthelmintic resistance. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1633

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):

Garretson, Pamela Donn. “Role of P-glycoprotein in Haemonchus contortus anthelmintic resistance.” 2009. Thesis, Texas A&M University. Accessed November 22, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-1633.

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

MLA Handbook (7th Edition):

Garretson, Pamela Donn. “Role of P-glycoprotein in Haemonchus contortus anthelmintic resistance.” 2009. Web. 22 Nov 2019.

Vancouver:

Garretson PD. Role of P-glycoprotein in Haemonchus contortus anthelmintic resistance. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1633.

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

Council of Science Editors:

Garretson PD. Role of P-glycoprotein in Haemonchus contortus anthelmintic resistance. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1633

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


Univerzitet u Beogradu

15. Dačević, Mirjana P., 1971-. Uloga purinskog nukleozidnog analoga-sulfinozina u inhibiciji rasta malignih ćelija neosetljivih na dejstvo hemioterapeutika.

Degree: Medicinski fakultet, 2014, Univerzitet u Beogradu

 <p>Medicina - Medicine p><p>Efikasno izlečenje tumora je veoma teško postići posebno kada se razvije višestruka rezistencija (MDR) na konvencionalnu antineoplastičnu terapiju. Visoka aktivnost Pglikoproteina (P‐gp)… (more)

Subjects/Keywords: sulfinosine; multidrug resistance; NSCLC; glioblastoma cells; P‐glycoprotein

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APA (6th Edition):

Dačević, Mirjana P., 1. (2014). Uloga purinskog nukleozidnog analoga-sulfinozina u inhibiciji rasta malignih ćelija neosetljivih na dejstvo hemioterapeutika. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:7906/bdef:Content/get

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

Chicago Manual of Style (16th Edition):

Dačević, Mirjana P., 1971-. “Uloga purinskog nukleozidnog analoga-sulfinozina u inhibiciji rasta malignih ćelija neosetljivih na dejstvo hemioterapeutika.” 2014. Thesis, Univerzitet u Beogradu. Accessed November 22, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:7906/bdef:Content/get.

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

MLA Handbook (7th Edition):

Dačević, Mirjana P., 1971-. “Uloga purinskog nukleozidnog analoga-sulfinozina u inhibiciji rasta malignih ćelija neosetljivih na dejstvo hemioterapeutika.” 2014. Web. 22 Nov 2019.

Vancouver:

Dačević, Mirjana P. 1. Uloga purinskog nukleozidnog analoga-sulfinozina u inhibiciji rasta malignih ćelija neosetljivih na dejstvo hemioterapeutika. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2019 Nov 22]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7906/bdef:Content/get.

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

Council of Science Editors:

Dačević, Mirjana P. 1. Uloga purinskog nukleozidnog analoga-sulfinozina u inhibiciji rasta malignih ćelija neosetljivih na dejstvo hemioterapeutika. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7906/bdef:Content/get

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


The Ohio State University

16. Ahn, Sunjoo. Novel Antimitotic Compounds with Potent <i>In Vitro</i> and <i>In Vivo</i> Antitumor Effects: the Use of Pharmacokinetics, Metabolism, Efficacy, and Toxicity Studies.

Degree: PhD, Pharmacy, 2010, The Ohio State University

 We identified novel indole derivatives inhibiting human cancer cell growth with nanomolar IC50 values. Thus, we studied the mechanism of anticancer effects, pharmacokinetics, <i>in vitro</i>… (more)

Subjects/Keywords: Pharmaceuticals; drug; discovery; tubulin; indole; P-glycoprotein; prostate cancer

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APA (6th Edition):

Ahn, S. (2010). Novel Antimitotic Compounds with Potent <i>In Vitro</i> and <i>In Vivo</i> Antitumor Effects: the Use of Pharmacokinetics, Metabolism, Efficacy, and Toxicity Studies. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1281966697

Chicago Manual of Style (16th Edition):

Ahn, Sunjoo. “Novel Antimitotic Compounds with Potent <i>In Vitro</i> and <i>In Vivo</i> Antitumor Effects: the Use of Pharmacokinetics, Metabolism, Efficacy, and Toxicity Studies.” 2010. Doctoral Dissertation, The Ohio State University. Accessed November 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1281966697.

MLA Handbook (7th Edition):

Ahn, Sunjoo. “Novel Antimitotic Compounds with Potent <i>In Vitro</i> and <i>In Vivo</i> Antitumor Effects: the Use of Pharmacokinetics, Metabolism, Efficacy, and Toxicity Studies.” 2010. Web. 22 Nov 2019.

Vancouver:

Ahn S. Novel Antimitotic Compounds with Potent <i>In Vitro</i> and <i>In Vivo</i> Antitumor Effects: the Use of Pharmacokinetics, Metabolism, Efficacy, and Toxicity Studies. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Nov 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281966697.

Council of Science Editors:

Ahn S. Novel Antimitotic Compounds with Potent <i>In Vitro</i> and <i>In Vivo</i> Antitumor Effects: the Use of Pharmacokinetics, Metabolism, Efficacy, and Toxicity Studies. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1281966697


The Ohio State University

17. Rozewski, Darlene M. Pharmacokinetics and P-glycoprotein-Mediated Transport of the Leading IMiDs in Mice.

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

 Lenalidomide and pomalidomide belong to a novel class of immunomodulatory (IMiD) drugs and have anti-angiogenic, anti-inflammatory, pro-erythropoietic and further anti-cancer activities. Both agents have shown… (more)

Subjects/Keywords: Pharmaceuticals; Lenalidomide; Pharmacokinetics; Mouse; P-glycoprotein; Disposition; Bioavailability; Transporter

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

APA (6th Edition):

Rozewski, D. M. (2012). Pharmacokinetics and P-glycoprotein-Mediated Transport of the Leading IMiDs in Mice. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1331144282

Chicago Manual of Style (16th Edition):

Rozewski, Darlene M. “Pharmacokinetics and P-glycoprotein-Mediated Transport of the Leading IMiDs in Mice.” 2012. Doctoral Dissertation, The Ohio State University. Accessed November 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1331144282.

MLA Handbook (7th Edition):

Rozewski, Darlene M. “Pharmacokinetics and P-glycoprotein-Mediated Transport of the Leading IMiDs in Mice.” 2012. Web. 22 Nov 2019.

Vancouver:

Rozewski DM. Pharmacokinetics and P-glycoprotein-Mediated Transport of the Leading IMiDs in Mice. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2019 Nov 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1331144282.

Council of Science Editors:

Rozewski DM. Pharmacokinetics and P-glycoprotein-Mediated Transport of the Leading IMiDs in Mice. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1331144282


Lincoln University

18. Bernardi, Giuliana R. ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool.

Degree: 2012, Lincoln University

 Earthworms are exposed to a variety of agrochemicals due to strict export requirements and maintenance of high productivity. Aporrectodea caliginosa (grey earthworm) is the most… (more)

Subjects/Keywords: earthworms; biomarkers; P-glycoprotein; toxicology; Aporrectodea caliginosa; agrochemicals; bioindicator

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APA (6th Edition):

Bernardi, G. R. (2012). ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/5034

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):

Bernardi, Giuliana R. “ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool.” 2012. Thesis, Lincoln University. Accessed November 22, 2019. http://hdl.handle.net/10182/5034.

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

MLA Handbook (7th Edition):

Bernardi, Giuliana R. “ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool.” 2012. Web. 22 Nov 2019.

Vancouver:

Bernardi GR. ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool. [Internet] [Thesis]. Lincoln University; 2012. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10182/5034.

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

Council of Science Editors:

Bernardi GR. ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool. [Thesis]. Lincoln University; 2012. Available from: http://hdl.handle.net/10182/5034

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


Penn State University

19. Tan, Su-fern. Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.

Degree: PhD, Molecular Medicine, 2013, Penn State University

 Acute myeloid leukemia (AML) is a heterogeneous disease that affects the differentiation of myeloid precursors. In normal hematopoiesis, hematopoietic stem cells committed to the myeloid… (more)

Subjects/Keywords: AML; Acid Ceramidase; Mcl-1; P-glycoprotein; NF-kB; sphingolipids

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APA (6th Edition):

Tan, S. (2013). Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/19626

Chicago Manual of Style (16th Edition):

Tan, Su-fern. “Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.” 2013. Doctoral Dissertation, Penn State University. Accessed November 22, 2019. https://etda.libraries.psu.edu/catalog/19626.

MLA Handbook (7th Edition):

Tan, Su-fern. “Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.” 2013. Web. 22 Nov 2019.

Vancouver:

Tan S. Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia. [Internet] [Doctoral dissertation]. Penn State University; 2013. [cited 2019 Nov 22]. Available from: https://etda.libraries.psu.edu/catalog/19626.

Council of Science Editors:

Tan S. Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia. [Doctoral Dissertation]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/19626


University of Manchester

20. Hamrang, Zahra. The application of image analysis extensions to processes of relevance to drug development.

Degree: PhD, 2013, University of Manchester

 In the past forty years advancements in fluorescence-based methods including imaging (e.g. confocal and multi-photon) and quantitative spectroscopies (e.g. Fluorescence Correlation Spectroscopy) have been applied… (more)

Subjects/Keywords: 615.1900724; Image analysis; Microscopy; Protein aggregation; P-glycoprotein

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APA (6th Edition):

Hamrang, Z. (2013). The application of image analysis extensions to processes of relevance to drug development. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-application-of-image-analysis-extensions-to-processes-of-relevance-to-drug-development(f68f0163-980d-4954-8fe9-a8a0f6ec5466).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574383

Chicago Manual of Style (16th Edition):

Hamrang, Zahra. “The application of image analysis extensions to processes of relevance to drug development.” 2013. Doctoral Dissertation, University of Manchester. Accessed November 22, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-application-of-image-analysis-extensions-to-processes-of-relevance-to-drug-development(f68f0163-980d-4954-8fe9-a8a0f6ec5466).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574383.

MLA Handbook (7th Edition):

Hamrang, Zahra. “The application of image analysis extensions to processes of relevance to drug development.” 2013. Web. 22 Nov 2019.

Vancouver:

Hamrang Z. The application of image analysis extensions to processes of relevance to drug development. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2019 Nov 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-application-of-image-analysis-extensions-to-processes-of-relevance-to-drug-development(f68f0163-980d-4954-8fe9-a8a0f6ec5466).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574383.

Council of Science Editors:

Hamrang Z. The application of image analysis extensions to processes of relevance to drug development. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-application-of-image-analysis-extensions-to-processes-of-relevance-to-drug-development(f68f0163-980d-4954-8fe9-a8a0f6ec5466).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574383


Louisiana State University

21. Linardi, Renata Lehn. Role of gastrointestinal multidrug resistance (MDR1) gene and P-glycoprotein (P-gp) in the oral absorption of methadone in horses.

Degree: PhD, Veterinary Medicine, 2010, Louisiana State University

 Methadone is a mu-opioid receptor agonist which is a very effective analgesic used to treat moderate to severe acute and chronic pain in humans. Due… (more)

Subjects/Keywords: Oral opioid absorption; Methadone; P-glycoprotein; MDR1 gene

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APA (6th Edition):

Linardi, R. L. (2010). Role of gastrointestinal multidrug resistance (MDR1) gene and P-glycoprotein (P-gp) in the oral absorption of methadone in horses. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-04212010-084044 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2938

Chicago Manual of Style (16th Edition):

Linardi, Renata Lehn. “Role of gastrointestinal multidrug resistance (MDR1) gene and P-glycoprotein (P-gp) in the oral absorption of methadone in horses.” 2010. Doctoral Dissertation, Louisiana State University. Accessed November 22, 2019. etd-04212010-084044 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2938.

MLA Handbook (7th Edition):

Linardi, Renata Lehn. “Role of gastrointestinal multidrug resistance (MDR1) gene and P-glycoprotein (P-gp) in the oral absorption of methadone in horses.” 2010. Web. 22 Nov 2019.

Vancouver:

Linardi RL. Role of gastrointestinal multidrug resistance (MDR1) gene and P-glycoprotein (P-gp) in the oral absorption of methadone in horses. [Internet] [Doctoral dissertation]. Louisiana State University; 2010. [cited 2019 Nov 22]. Available from: etd-04212010-084044 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2938.

Council of Science Editors:

Linardi RL. Role of gastrointestinal multidrug resistance (MDR1) gene and P-glycoprotein (P-gp) in the oral absorption of methadone in horses. [Doctoral Dissertation]. Louisiana State University; 2010. Available from: etd-04212010-084044 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2938


University of Sydney

22. Brzozowska, Natalia Izabela. Advancing ABC transporter biology: from cannabinoid interactions to neurobehavioural function .

Degree: 2017, University of Sydney

 Chapter 1 reviews the scientific literature and justifies the 3 main aims of this thesis. ATP-binding cassette (ABC) transporters are membrane bound efflux proteins located… (more)

Subjects/Keywords: ABC transporters; P-glycoprotein; Cannabinoids; Schizophrenia; Depression; Epilepsy

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APA (6th Edition):

Brzozowska, N. I. (2017). Advancing ABC transporter biology: from cannabinoid interactions to neurobehavioural function . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16997

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):

Brzozowska, Natalia Izabela. “Advancing ABC transporter biology: from cannabinoid interactions to neurobehavioural function .” 2017. Thesis, University of Sydney. Accessed November 22, 2019. http://hdl.handle.net/2123/16997.

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

MLA Handbook (7th Edition):

Brzozowska, Natalia Izabela. “Advancing ABC transporter biology: from cannabinoid interactions to neurobehavioural function .” 2017. Web. 22 Nov 2019.

Vancouver:

Brzozowska NI. Advancing ABC transporter biology: from cannabinoid interactions to neurobehavioural function . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2123/16997.

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

Council of Science Editors:

Brzozowska NI. Advancing ABC transporter biology: from cannabinoid interactions to neurobehavioural function . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/16997

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


Montana Tech

23. Lacher, Sarah Elizabeth. P-GLYCOPROTEIN TRANSPORT IN PESTICIDE PHARMACOKINETICS AND TOXICITY: INVESTIGATING A LINK TO PARKINSON'S DISEASE RISK.

Degree: PhD, 2013, Montana Tech

  Variation in the gene that encodes P-glycoprotein (P-gp), ABCB1, has been associated with Parkinson's disease risk. The aim of my research was to evaluate… (more)

Subjects/Keywords: PARKINSON'S DISEASE; PESTICIDE; P-GLYCOPROTEIN TRANSPORT; PHARMACOKINETICS; TOXICITY

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APA (6th Edition):

Lacher, S. E. (2013). P-GLYCOPROTEIN TRANSPORT IN PESTICIDE PHARMACOKINETICS AND TOXICITY: INVESTIGATING A LINK TO PARKINSON'S DISEASE RISK. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/4135

Chicago Manual of Style (16th Edition):

Lacher, Sarah Elizabeth. “P-GLYCOPROTEIN TRANSPORT IN PESTICIDE PHARMACOKINETICS AND TOXICITY: INVESTIGATING A LINK TO PARKINSON'S DISEASE RISK.” 2013. Doctoral Dissertation, Montana Tech. Accessed November 22, 2019. https://scholarworks.umt.edu/etd/4135.

MLA Handbook (7th Edition):

Lacher, Sarah Elizabeth. “P-GLYCOPROTEIN TRANSPORT IN PESTICIDE PHARMACOKINETICS AND TOXICITY: INVESTIGATING A LINK TO PARKINSON'S DISEASE RISK.” 2013. Web. 22 Nov 2019.

Vancouver:

Lacher SE. P-GLYCOPROTEIN TRANSPORT IN PESTICIDE PHARMACOKINETICS AND TOXICITY: INVESTIGATING A LINK TO PARKINSON'S DISEASE RISK. [Internet] [Doctoral dissertation]. Montana Tech; 2013. [cited 2019 Nov 22]. Available from: https://scholarworks.umt.edu/etd/4135.

Council of Science Editors:

Lacher SE. P-GLYCOPROTEIN TRANSPORT IN PESTICIDE PHARMACOKINETICS AND TOXICITY: INVESTIGATING A LINK TO PARKINSON'S DISEASE RISK. [Doctoral Dissertation]. Montana Tech; 2013. Available from: https://scholarworks.umt.edu/etd/4135


University of the Western Cape

24. Pillay, Leeshan. The integrated effects of selected inducers of endoplasmic reticulum stress, the unfolded protein response and apoptosis on P-Glycoprotein mediated drug resistance in MCF-7 breast carcinoma cells .

Degree: 2015, University of the Western Cape

 Purpose: One of the leading causes of death reported in women worldwide is breast cancer. Manytumours, including breast cancer, associated with poor prognosis, have received… (more)

Subjects/Keywords: Breast cancer; P-Glycoprotein; Apoptosis; Endoplasmic reticulum stress; Multidrug resistance

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APA (6th Edition):

Pillay, L. (2015). The integrated effects of selected inducers of endoplasmic reticulum stress, the unfolded protein response and apoptosis on P-Glycoprotein mediated drug resistance in MCF-7 breast carcinoma cells . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4459

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):

Pillay, Leeshan. “The integrated effects of selected inducers of endoplasmic reticulum stress, the unfolded protein response and apoptosis on P-Glycoprotein mediated drug resistance in MCF-7 breast carcinoma cells .” 2015. Thesis, University of the Western Cape. Accessed November 22, 2019. http://hdl.handle.net/11394/4459.

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

MLA Handbook (7th Edition):

Pillay, Leeshan. “The integrated effects of selected inducers of endoplasmic reticulum stress, the unfolded protein response and apoptosis on P-Glycoprotein mediated drug resistance in MCF-7 breast carcinoma cells .” 2015. Web. 22 Nov 2019.

Vancouver:

Pillay L. The integrated effects of selected inducers of endoplasmic reticulum stress, the unfolded protein response and apoptosis on P-Glycoprotein mediated drug resistance in MCF-7 breast carcinoma cells . [Internet] [Thesis]. University of the Western Cape; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/11394/4459.

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

Council of Science Editors:

Pillay L. The integrated effects of selected inducers of endoplasmic reticulum stress, the unfolded protein response and apoptosis on P-Glycoprotein mediated drug resistance in MCF-7 breast carcinoma cells . [Thesis]. University of the Western Cape; 2015. Available from: http://hdl.handle.net/11394/4459

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


University of Adelaide

25. Barratt, Daniel Thomas. Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence.

Degree: 2010, University of Adelaide

 Opioid dependence is a significant public health problem. Whilst long-term opioid maintenance is the most cost-effective approach for treating opioid dependence, the safe and effective… (more)

Subjects/Keywords: opioid dependence; methadone; buprenorphine; P-glycoprotein; ABCB1; MDR1

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

APA (6th Edition):

Barratt, D. T. (2010). Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/64812

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):

Barratt, Daniel Thomas. “Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence.” 2010. Thesis, University of Adelaide. Accessed November 22, 2019. http://hdl.handle.net/2440/64812.

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

MLA Handbook (7th Edition):

Barratt, Daniel Thomas. “Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence.” 2010. Web. 22 Nov 2019.

Vancouver:

Barratt DT. Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/2440/64812.

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

Council of Science Editors:

Barratt DT. Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/64812

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


Cornell University

26. Crawford, Lindsey. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery .

Degree: 2015, Cornell University

 Drug development for the central nervous system (CNS) has struggled to reach clinical approval. One reason many drugs do not advance into clinical applications is… (more)

Subjects/Keywords: P-glycoprotein; Targeted Drug Delivery; Blood Brain Barrier

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APA (6th Edition):

Crawford, L. (2015). Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/41124

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):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery .” 2015. Thesis, Cornell University. Accessed November 22, 2019. http://hdl.handle.net/1813/41124.

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

MLA Handbook (7th Edition):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery .” 2015. Web. 22 Nov 2019.

Vancouver:

Crawford L. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1813/41124.

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

Council of Science Editors:

Crawford L. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41124

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


University College Cork

27. O'Brien, Fionn E. P-glycoprotein inhibition as a strategy to increase drug delivery across the blood-brain barrier: focus on antidepressants.

Degree: 2013, University College Cork

 Depression is among the leading causes of disability worldwide. Currently available antidepressant drugs have unsatisfactory efficacy, with up to 60% of depressed patients failing to… (more)

Subjects/Keywords: Antidepressant; Blood-brain barrier; Drug delivery; P-glycoprotein; Treatment-resistant depression

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APA (6th Edition):

O'Brien, F. E. (2013). P-glycoprotein inhibition as a strategy to increase drug delivery across the blood-brain barrier: focus on antidepressants. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/1400

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):

O'Brien, Fionn E. “P-glycoprotein inhibition as a strategy to increase drug delivery across the blood-brain barrier: focus on antidepressants.” 2013. Thesis, University College Cork. Accessed November 22, 2019. http://hdl.handle.net/10468/1400.

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

MLA Handbook (7th Edition):

O'Brien, Fionn E. “P-glycoprotein inhibition as a strategy to increase drug delivery across the blood-brain barrier: focus on antidepressants.” 2013. Web. 22 Nov 2019.

Vancouver:

O'Brien FE. P-glycoprotein inhibition as a strategy to increase drug delivery across the blood-brain barrier: focus on antidepressants. [Internet] [Thesis]. University College Cork; 2013. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/10468/1400.

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

Council of Science Editors:

O'Brien FE. P-glycoprotein inhibition as a strategy to increase drug delivery across the blood-brain barrier: focus on antidepressants. [Thesis]. University College Cork; 2013. Available from: http://hdl.handle.net/10468/1400

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


University of Iowa

28. Sheehy, Ryan Michael. Mechanisms of the anti-proliferative actions of the schweinfurthins in cancer cells.

Degree: PhD, Pharmacology, 2015, University of Iowa

  Schweinfurthins are intriguing natural product chemotherapeutics due to their potent yet selective activity and their unknown mechanism of growth inhibition in cancer. Much progress… (more)

Subjects/Keywords: publicabstract; ABCA1; cancer; EGFR; P-glycoprotein; schweinfurthin; verapamil; Pharmacology

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

APA (6th Edition):

Sheehy, R. M. (2015). Mechanisms of the anti-proliferative actions of the schweinfurthins in cancer cells. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1752

Chicago Manual of Style (16th Edition):

Sheehy, Ryan Michael. “Mechanisms of the anti-proliferative actions of the schweinfurthins in cancer cells.” 2015. Doctoral Dissertation, University of Iowa. Accessed November 22, 2019. https://ir.uiowa.edu/etd/1752.

MLA Handbook (7th Edition):

Sheehy, Ryan Michael. “Mechanisms of the anti-proliferative actions of the schweinfurthins in cancer cells.” 2015. Web. 22 Nov 2019.

Vancouver:

Sheehy RM. Mechanisms of the anti-proliferative actions of the schweinfurthins in cancer cells. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2019 Nov 22]. Available from: https://ir.uiowa.edu/etd/1752.

Council of Science Editors:

Sheehy RM. Mechanisms of the anti-proliferative actions of the schweinfurthins in cancer cells. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/1752


University of Manitoba

29. Pogorzelec, Michael P.J. Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines.

Degree: Pharmacology and Therapeutics, 2015, University of Manitoba

 Little is known about potential influences of kinase pathway modulation on expression and activity of P-glycoprotein (P-gp). A protein kinase inhibitor (PKI) library was screened,… (more)

Subjects/Keywords: P-glycoprotein; Protein kinase inhibitors; Blood Brain Barrier

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

APA (6th Edition):

Pogorzelec, M. P. J. (2015). Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30206

Chicago Manual of Style (16th Edition):

Pogorzelec, Michael P J. “Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines.” 2015. Masters Thesis, University of Manitoba. Accessed November 22, 2019. http://hdl.handle.net/1993/30206.

MLA Handbook (7th Edition):

Pogorzelec, Michael P J. “Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines.” 2015. Web. 22 Nov 2019.

Vancouver:

Pogorzelec MPJ. Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines. [Internet] [Masters thesis]. University of Manitoba; 2015. [cited 2019 Nov 22]. Available from: http://hdl.handle.net/1993/30206.

Council of Science Editors:

Pogorzelec MPJ. Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines. [Masters Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/30206


University of Guelph

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

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

APA (6th Edition):

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

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):

Vitsupakorn, Danoo. “Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter .” 2014. Thesis, University of Guelph. Accessed November 22, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398.

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

MLA Handbook (7th Edition):

Vitsupakorn, Danoo. “Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter .” 2014. Web. 22 Nov 2019.

Vancouver:

Vitsupakorn D. Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter . [Internet] [Thesis]. University of Guelph; 2014. [cited 2019 Nov 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398.

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

Council of Science Editors:

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

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

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