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Dates: 2010 – 2014

You searched for subject:( P glycoprotein). Showing records 1 – 30 of 66 total matches.

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University of Texas Medical Branch – Galveston

1. [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 June 17, 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. 17 Jun 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 Jun 17]. 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 Houston

2. 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 June 17, 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. 17 Jun 2019.

Vancouver:

Yang Z1. Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches. [Internet] [Thesis]. University of Houston; 2012. [cited 2019 Jun 17]. 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

3. 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 June 17, 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. 17 Jun 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 Jun 17]. 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

4. 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 June 17, 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. 17 Jun 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 Jun 17]. 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


Dalhousie University

5. 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 June 17, 2019. http://hdl.handle.net/10222/54084.

MLA Handbook (7th Edition):

Wang, Yan. “Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid.” 2014. Web. 17 Jun 2019.

Vancouver:

Wang Y. Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2019 Jun 17]. 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


University of Guelph

6. Clay, Adam Thomas. The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions .

Degree: 2011, University of Guelph

 The ABC protein P-glycoprotein (Pgp, ABCB1) transports many structurally diverse substrates from the lipid bilayer. Previous studies demonstrated the importance of the membrane environment, but… (more)

Subjects/Keywords: P-glycoprotein; Pgp; ABCB1; drug binding; drug transport

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APA (6th Edition):

Clay, A. T. (2011). The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3196

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):

Clay, Adam Thomas. “The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions .” 2011. Thesis, University of Guelph. Accessed June 17, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3196.

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

MLA Handbook (7th Edition):

Clay, Adam Thomas. “The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions .” 2011. Web. 17 Jun 2019.

Vancouver:

Clay AT. The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions . [Internet] [Thesis]. University of Guelph; 2011. [cited 2019 Jun 17]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3196.

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

Council of Science Editors:

Clay AT. The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions . [Thesis]. University of Guelph; 2011. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3196

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


University of Guelph

7. 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 (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 June 17, 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. 17 Jun 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 Jun 17]. 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


Univerzitet u Beogradu

8. 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 June 17, 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. 17 Jun 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 Jun 17]. 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

9. 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 June 17, 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. 17 Jun 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 Jun 17]. 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

10. 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 (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 June 17, 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. 17 Jun 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 Jun 17]. 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

11. 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 June 17, 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. 17 Jun 2019.

Vancouver:

Bernardi GR. ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool. [Internet] [Thesis]. Lincoln University; 2012. [cited 2019 Jun 17]. 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

12. 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 June 17, 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. 17 Jun 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 Jun 17]. 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

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

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 June 17, 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. 17 Jun 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 Jun 17]. 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

14. 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 June 17, 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. 17 Jun 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 Jun 17]. 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


Montana Tech

15. 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 June 17, 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. 17 Jun 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 Jun 17]. 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 Adelaide

16. 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 (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 June 17, 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. 17 Jun 2019.

Vancouver:

Barratt DT. Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2019 Jun 17]. 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


University College Cork

17. 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 June 17, 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. 17 Jun 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 Jun 17]. 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

18. Durk, Robert Matthew. Role of the Vitamin D Receptor in MDR1/P-glycoprotein Regulation at the Blood-brain Barrier.

Degree: PhD, 2014, University of Toronto

 The blood-brain barrier (BBB) presents a major obstacle for drugs targeting the brain. Drugs that are small or lipophilic enough can penetrate the physical barrier,… (more)

Subjects/Keywords: blood-brain barrier; P-glycoprotein; regulation; vitamin D receptor; 0572

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APA (6th Edition):

Durk, R. M. (2014). Role of the Vitamin D Receptor in MDR1/P-glycoprotein Regulation at the Blood-brain Barrier. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/67621

Chicago Manual of Style (16th Edition):

Durk, Robert Matthew. “Role of the Vitamin D Receptor in MDR1/P-glycoprotein Regulation at the Blood-brain Barrier.” 2014. Doctoral Dissertation, University of Toronto. Accessed June 17, 2019. http://hdl.handle.net/1807/67621.

MLA Handbook (7th Edition):

Durk, Robert Matthew. “Role of the Vitamin D Receptor in MDR1/P-glycoprotein Regulation at the Blood-brain Barrier.” 2014. Web. 17 Jun 2019.

Vancouver:

Durk RM. Role of the Vitamin D Receptor in MDR1/P-glycoprotein Regulation at the Blood-brain Barrier. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/1807/67621.

Council of Science Editors:

Durk RM. Role of the Vitamin D Receptor in MDR1/P-glycoprotein Regulation at the Blood-brain Barrier. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67621


University of Toronto

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

Degree: PhD, 2014, University of Toronto

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Lam, Jessica Fung Chi. “Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions.” 2014. Doctoral Dissertation, University of Toronto. Accessed June 17, 2019. http://hdl.handle.net/1807/68430.

MLA Handbook (7th Edition):

Lam, Jessica Fung Chi. “Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions.” 2014. Web. 17 Jun 2019.

Vancouver:

Lam JFC. Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/1807/68430.

Council of Science Editors:

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


University of Arizona

20. Sanchez Covarrubias, Lucy. NSAIDs Modulate Morphine Transport at the Blood-Brain Barrier: A Role for P-glycoprotein .

Degree: 2013, University of Arizona

 Our laboratory has previously demonstrated that experimental peripheral inflammatory pain (PIP), induced by subcutaneous plantar injection of λ-carrageenan in Sprague Dawley rats, results in increased… (more)

Subjects/Keywords: Diclofenac; Morphine; P-glycoprotein; Trafficking; Medical Pharmacology; Blood-Brain Barrier

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APA (6th Edition):

Sanchez Covarrubias, L. (2013). NSAIDs Modulate Morphine Transport at the Blood-Brain Barrier: A Role for P-glycoprotein . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/294027

Chicago Manual of Style (16th Edition):

Sanchez Covarrubias, Lucy. “NSAIDs Modulate Morphine Transport at the Blood-Brain Barrier: A Role for P-glycoprotein .” 2013. Doctoral Dissertation, University of Arizona. Accessed June 17, 2019. http://hdl.handle.net/10150/294027.

MLA Handbook (7th Edition):

Sanchez Covarrubias, Lucy. “NSAIDs Modulate Morphine Transport at the Blood-Brain Barrier: A Role for P-glycoprotein .” 2013. Web. 17 Jun 2019.

Vancouver:

Sanchez Covarrubias L. NSAIDs Modulate Morphine Transport at the Blood-Brain Barrier: A Role for P-glycoprotein . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/10150/294027.

Council of Science Editors:

Sanchez Covarrubias L. NSAIDs Modulate Morphine Transport at the Blood-Brain Barrier: A Role for P-glycoprotein . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/294027


University of Alberta

21. Binkhathlan, Ziyad. Development of block copolymer based nanocarriers for the solubilization and delivery of valspodar.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2011, University of Alberta

 One of the major causes of failure in cancer chemotherapy is multidrug resistance (MDR), where cancer cells become resistant to different types of anticancer drugs.… (more)

Subjects/Keywords: valspodar; cancer; pharmacokinetics; P-glycoprotein; polymeric micelles; polymeric vesicles; multi-drug resistance; block copolymer

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APA (6th Edition):

Binkhathlan, Z. (2011). Development of block copolymer based nanocarriers for the solubilization and delivery of valspodar. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/08612n954

Chicago Manual of Style (16th Edition):

Binkhathlan, Ziyad. “Development of block copolymer based nanocarriers for the solubilization and delivery of valspodar.” 2011. Doctoral Dissertation, University of Alberta. Accessed June 17, 2019. https://era.library.ualberta.ca/files/08612n954.

MLA Handbook (7th Edition):

Binkhathlan, Ziyad. “Development of block copolymer based nanocarriers for the solubilization and delivery of valspodar.” 2011. Web. 17 Jun 2019.

Vancouver:

Binkhathlan Z. Development of block copolymer based nanocarriers for the solubilization and delivery of valspodar. [Internet] [Doctoral dissertation]. University of Alberta; 2011. [cited 2019 Jun 17]. Available from: https://era.library.ualberta.ca/files/08612n954.

Council of Science Editors:

Binkhathlan Z. Development of block copolymer based nanocarriers for the solubilization and delivery of valspodar. [Doctoral Dissertation]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/08612n954


University of Guelph

22. Ward, David. Characterizing drug interactions in the substrate binding pocket of the P-glycoprotein multidrug efflux pump .

Degree: 2012, University of Guelph

P-glycoprotein (Pgp, ABCB1) is a polyspecific efflux transporter implicated in multidrug resistance in human cancers. In this study, tetramethylrhodamine-5-carbonyl azide (AzTMR) was covalently crosslinked to… (more)

Subjects/Keywords: P-glycoprotein; Pgp; drug resistance; cancer; tumour; MDR; drug binding; drug transport; multidrug resistance; chemotherapy

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APA (6th Edition):

Ward, D. (2012). Characterizing drug interactions in the substrate binding pocket of the P-glycoprotein multidrug efflux pump . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3309

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):

Ward, David. “Characterizing drug interactions in the substrate binding pocket of the P-glycoprotein multidrug efflux pump .” 2012. Thesis, University of Guelph. Accessed June 17, 2019. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3309.

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

MLA Handbook (7th Edition):

Ward, David. “Characterizing drug interactions in the substrate binding pocket of the P-glycoprotein multidrug efflux pump .” 2012. Web. 17 Jun 2019.

Vancouver:

Ward D. Characterizing drug interactions in the substrate binding pocket of the P-glycoprotein multidrug efflux pump . [Internet] [Thesis]. University of Guelph; 2012. [cited 2019 Jun 17]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3309.

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

Council of Science Editors:

Ward D. Characterizing drug interactions in the substrate binding pocket of the P-glycoprotein multidrug efflux pump . [Thesis]. University of Guelph; 2012. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3309

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


Univerzitet u Beogradu

23. Podolski-Renić, Ana. 1980-. Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu.

Degree: Biološki fakultet, 2014, Univerzitet u Beogradu

 <p>Molekularna onkologija - Kancerogeneza / Molecular oncology - Cancerogenesis p><p>Glavni uzrok neuspeha hemioterapije u lečenju kancera je pojava višestruke (engl. „multi-drug“) rezistencije (MDR). Efikasnost paklitaksela… (more)

Subjects/Keywords: Multi-drug resistance (MDR); paclitaxel (PTX); colon cancer; glioblastoma; P-glycoprotein; anti-cancer agents

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APA (6th Edition):

Podolski-Renić, A. 1. (2014). Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:7135/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):

Podolski-Renić, Ana 1980-. “Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu.” 2014. Thesis, Univerzitet u Beogradu. Accessed June 17, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:7135/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):

Podolski-Renić, Ana 1980-. “Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu.” 2014. Web. 17 Jun 2019.

Vancouver:

Podolski-Renić A1. Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2019 Jun 17]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7135/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:

Podolski-Renić A1. Uspostavljanje rezistentnih tumorskih ćelijskih linija kao modela za testiranje novih hemioterapeutika : molekularna karakterizacija rezistencije nastale dugotrajnim izlaganjem paklitakselu. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7135/bdef:Content/get

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


Universidade do Rio Grande do Sul

24. Baja, Karine Gehlen. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.

Degree: 2013, Universidade do Rio Grande do Sul

 A P-glicoproteína (P-gp) é uma transportadora transmembrana de múltiplos fármacos, produto do gene MDR1 (ABCB1). A P-gp contribui para a função de barreira de vários… (more)

Subjects/Keywords: Tramadol; MDR1; P-glycoprotein; Farmacocinética; Genetic mutation; Farmacogenética; Gogs; Genes MDR; Cães; Sustained release tramadol

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APA (6th Edition):

Baja, K. G. (2013). Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/79520

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):

Baja, Karine Gehlen. “Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.” 2013. Thesis, Universidade do Rio Grande do Sul. Accessed June 17, 2019. http://hdl.handle.net/10183/79520.

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

MLA Handbook (7th Edition):

Baja, Karine Gehlen. “Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1.” 2013. Web. 17 Jun 2019.

Vancouver:

Baja KG. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/10183/79520.

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

Council of Science Editors:

Baja KG. Farmacocinética do cloridrato de tramadol administrado por via oral em cães com a mutação nt230(del4) no gene MDR1. [Thesis]. Universidade do Rio Grande do Sul; 2013. Available from: http://hdl.handle.net/10183/79520

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


University of Toronto

25. Chamberlain, Graham Ross. Mitochondria-targeted Doxorubicin is Active and Resistant to Drug Efflux.

Degree: 2012, University of Toronto

 <p>Several families of highly effective anticancer drugs are selectively toxic to cancer cells because they interfere with nucleic acids synthesis. Many such drugs are pumped… (more)

Subjects/Keywords: Doxorubicin; Drug Resistance; P-glycoprotein; Drug Efflux; Topoisomerase II; Mitochondria; Mitochondria Penetrating Peptides; 0572

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APA (6th Edition):

Chamberlain, G. R. (2012). Mitochondria-targeted Doxorubicin is Active and Resistant to Drug Efflux. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33360

Chicago Manual of Style (16th Edition):

Chamberlain, Graham Ross. “Mitochondria-targeted Doxorubicin is Active and Resistant to Drug Efflux.” 2012. Masters Thesis, University of Toronto. Accessed June 17, 2019. http://hdl.handle.net/1807/33360.

MLA Handbook (7th Edition):

Chamberlain, Graham Ross. “Mitochondria-targeted Doxorubicin is Active and Resistant to Drug Efflux.” 2012. Web. 17 Jun 2019.

Vancouver:

Chamberlain GR. Mitochondria-targeted Doxorubicin is Active and Resistant to Drug Efflux. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/1807/33360.

Council of Science Editors:

Chamberlain GR. Mitochondria-targeted Doxorubicin is Active and Resistant to Drug Efflux. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33360

26. Dias, Carlos André Ribeiro. Possible emodepside toxicosis in a Collie with MDR1 gene mutation.

Degree: 2014, RCAAP

 <p>The multi-drug resistance gene 1 (MDR1) is responsible for encoding an efflux transport protein designated P-glycoprotein (P-gp). The P-gp is expressed in various tissues such… (more)

Subjects/Keywords: Collie; Emodepside; Adverse Drug Reactions; MDR 1 gene mutation; ABCB 1 gene; P Glycoprotein

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APA (6th Edition):

Dias, C. A. R. (2014). Possible emodepside toxicosis in a Collie with MDR1 gene mutation. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/16628

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):

Dias, Carlos André Ribeiro. “Possible emodepside toxicosis in a Collie with MDR1 gene mutation.” 2014. Thesis, RCAAP. Accessed June 17, 2019. https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/16628.

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

MLA Handbook (7th Edition):

Dias, Carlos André Ribeiro. “Possible emodepside toxicosis in a Collie with MDR1 gene mutation.” 2014. Web. 17 Jun 2019.

Vancouver:

Dias CAR. Possible emodepside toxicosis in a Collie with MDR1 gene mutation. [Internet] [Thesis]. RCAAP; 2014. [cited 2019 Jun 17]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/16628.

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

Council of Science Editors:

Dias CAR. Possible emodepside toxicosis in a Collie with MDR1 gene mutation. [Thesis]. RCAAP; 2014. Available from: https://www.rcaap.pt/detail.jsp?id=oai:comum.rcaap.pt:10400.26/16628

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


University of Minnesota

27. Agarwal, Sagar Suresh. Improving delivery of molecularly targeted agents to glioma.

Degree: PhD, Pharmaceutics, 2011, University of Minnesota

 Treatment of glioblastoma multiforme is at a crossroads. Promising new molecularly-targeted agents have failed to show any significant clinical benefit. Treatment is particularly challenging since… (more)

Subjects/Keywords: BCRP; Blood Brain Barrier; Glioblastoma; Glioma; Molecularly Targeted Agents; P-glycoprotein; Pharmaceutics

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

APA (6th Edition):

Agarwal, S. S. (2011). Improving delivery of molecularly targeted agents to glioma. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/109325

Chicago Manual of Style (16th Edition):

Agarwal, Sagar Suresh. “Improving delivery of molecularly targeted agents to glioma.” 2011. Doctoral Dissertation, University of Minnesota. Accessed June 17, 2019. http://purl.umn.edu/109325.

MLA Handbook (7th Edition):

Agarwal, Sagar Suresh. “Improving delivery of molecularly targeted agents to glioma.” 2011. Web. 17 Jun 2019.

Vancouver:

Agarwal SS. Improving delivery of molecularly targeted agents to glioma. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2019 Jun 17]. Available from: http://purl.umn.edu/109325.

Council of Science Editors:

Agarwal SS. Improving delivery of molecularly targeted agents to glioma. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/109325

28. Alhaddad, Hisham. Etude expérimentale de la variabilité des effets respiratoires de la buprénorphine : rôle de la P-glycoprotéine et de l’acquisition d’une tolérance aux opioïdes : Experimental study of variability of buprenorphine-related respiratory effects : role of P-glycoprotein and tolerance acquisition.

Degree: Docteur es, Toxicologie, 2013, Université Paris Descartes – Paris V

 <p>La buprénorphine (BUP) peut être responsable d’une dépression respiratoire à l’origine d’intoxications graves parfois mortels. Cependant, les mécanismes exacts de ces effets respiratoires délétères ne… (more)

Subjects/Keywords: P-glycoprotéine; Buprénorphine; Variabilité; Dépression respiratoire; Pléthysmographie; Souris; P-glycoprotein; Buprenorphine; Variability; Respiratory depression; Plethysmography; Mice; 615.9

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

APA (6th Edition):

Alhaddad, H. (2013). Etude expérimentale de la variabilité des effets respiratoires de la buprénorphine : rôle de la P-glycoprotéine et de l’acquisition d’une tolérance aux opioïdes : Experimental study of variability of buprenorphine-related respiratory effects : role of P-glycoprotein and tolerance acquisition. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05P608

Chicago Manual of Style (16th Edition):

Alhaddad, Hisham. “Etude expérimentale de la variabilité des effets respiratoires de la buprénorphine : rôle de la P-glycoprotéine et de l’acquisition d’une tolérance aux opioïdes : Experimental study of variability of buprenorphine-related respiratory effects : role of P-glycoprotein and tolerance acquisition.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed June 17, 2019. http://www.theses.fr/2013PA05P608.

MLA Handbook (7th Edition):

Alhaddad, Hisham. “Etude expérimentale de la variabilité des effets respiratoires de la buprénorphine : rôle de la P-glycoprotéine et de l’acquisition d’une tolérance aux opioïdes : Experimental study of variability of buprenorphine-related respiratory effects : role of P-glycoprotein and tolerance acquisition.” 2013. Web. 17 Jun 2019.

Vancouver:

Alhaddad H. Etude expérimentale de la variabilité des effets respiratoires de la buprénorphine : rôle de la P-glycoprotéine et de l’acquisition d’une tolérance aux opioïdes : Experimental study of variability of buprenorphine-related respiratory effects : role of P-glycoprotein and tolerance acquisition. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2019 Jun 17]. Available from: http://www.theses.fr/2013PA05P608.

Council of Science Editors:

Alhaddad H. Etude expérimentale de la variabilité des effets respiratoires de la buprénorphine : rôle de la P-glycoprotéine et de l’acquisition d’une tolérance aux opioïdes : Experimental study of variability of buprenorphine-related respiratory effects : role of P-glycoprotein and tolerance acquisition. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05P608


Univerzitet u Beogradu

29. Jadranin, Milka B., 1971-. Izolovanje, karakterizacija i biološka aktivnost jatrofanskih diterpena iz Euphorbia dendroides L.

Degree: Hemijski fakultet, 2014, Univerzitet u Beogradu

 <p>Hemija - Organska hemija / Chemistry - Organic Chemistry p><p>Rod Euphorbia, sa više od 2.000 vrsta jednogodišnjih, dvogodišnjih ili višegodišnjih cvetnica koje su članovi familije… (more)

Subjects/Keywords: Euphorbia dendroides; Euphorbiaceae; Isolation; Characterization; Jatrophanes; Euphodendrophanes AS; P-glycoprotein (P-gp); Multidrug resistance; (MDR); Tubulin.

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APA (6th Edition):

Jadranin, Milka B., 1. (2014). Izolovanje, karakterizacija i biološka aktivnost jatrofanskih diterpena iz Euphorbia dendroides L. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:7449/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):

Jadranin, Milka B., 1971-. “Izolovanje, karakterizacija i biološka aktivnost jatrofanskih diterpena iz Euphorbia dendroides L.” 2014. Thesis, Univerzitet u Beogradu. Accessed June 17, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:7449/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):

Jadranin, Milka B., 1971-. “Izolovanje, karakterizacija i biološka aktivnost jatrofanskih diterpena iz Euphorbia dendroides L.” 2014. Web. 17 Jun 2019.

Vancouver:

Jadranin, Milka B. 1. Izolovanje, karakterizacija i biološka aktivnost jatrofanskih diterpena iz Euphorbia dendroides L. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2019 Jun 17]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7449/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:

Jadranin, Milka B. 1. Izolovanje, karakterizacija i biološka aktivnost jatrofanskih diterpena iz Euphorbia dendroides L. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7449/bdef:Content/get

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


Johannes Gutenberg Universität Mainz

30. Holthöwer, David. Einfluss der Modulation von P-Glykoprotein (P-gp) auf die Verfügbarkeit und Wirksamkeit der pharmakologischen Behandlung psychiatrischer Erkrankungen im Tiermodell.

Degree: 2011, Johannes Gutenberg Universität Mainz

P-Glykoprotein (P-gp) ist ein ATP-verbrauchender Transporter, der in Organschranken exprimiert wird, um Fremdstoffe auszuschleusen, darunter auch Psychopharmaka. Im Rahmen dieser Arbeit wurde im Tiermodell der… (more)

Subjects/Keywords: P-Glykoprotein; Transport; Pharmakokinetik; Pharmakodynamik; Antipsychotika; P-glycoprotein; transport; pharmacokinetics; pharmacodynamics; antipsychotic; Natural sciences and mathematics

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

APA (6th Edition):

Holthöwer, D. (2011). Einfluss der Modulation von P-Glykoprotein (P-gp) auf die Verfügbarkeit und Wirksamkeit der pharmakologischen Behandlung psychiatrischer Erkrankungen im Tiermodell. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2011/2802/

Chicago Manual of Style (16th Edition):

Holthöwer, David. “Einfluss der Modulation von P-Glykoprotein (P-gp) auf die Verfügbarkeit und Wirksamkeit der pharmakologischen Behandlung psychiatrischer Erkrankungen im Tiermodell.” 2011. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed June 17, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2011/2802/.

MLA Handbook (7th Edition):

Holthöwer, David. “Einfluss der Modulation von P-Glykoprotein (P-gp) auf die Verfügbarkeit und Wirksamkeit der pharmakologischen Behandlung psychiatrischer Erkrankungen im Tiermodell.” 2011. Web. 17 Jun 2019.

Vancouver:

Holthöwer D. Einfluss der Modulation von P-Glykoprotein (P-gp) auf die Verfügbarkeit und Wirksamkeit der pharmakologischen Behandlung psychiatrischer Erkrankungen im Tiermodell. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2011. [cited 2019 Jun 17]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2802/.

Council of Science Editors:

Holthöwer D. Einfluss der Modulation von P-Glykoprotein (P-gp) auf die Verfügbarkeit und Wirksamkeit der pharmakologischen Behandlung psychiatrischer Erkrankungen im Tiermodell. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2011. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2011/2802/

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