Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(P glycoprotein). Showing records 1 – 30 of 181 total matches.

[1] [2] [3] [4] [5] [6] [7]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Country

▼ Search Limiters


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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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


Oregon State University

2. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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

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

Degree: Pharmaceutics, Pharmaceutics, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Yang, Zhen 1982-. “Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches.” 2012. Doctoral Dissertation, University of Houston. Accessed January 22, 2021. http://hdl.handle.net/10657/1648.

MLA Handbook (7th Edition):

Yang, Zhen 1982-. “Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches.” 2012. Web. 22 Jan 2021.

Vancouver:

Yang Z1. Improvement of Oral Bioavailability of Ginsenosides via Mechanism-based Biopharmaceutical Approaches. [Internet] [Doctoral dissertation]. University of Houston; 2012. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/10657/1648.

Council of Science Editors:

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


University of Sydney

4. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Seebacher NA. Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones . [Internet] [Thesis]. University of Sydney; 2015. [cited 2021 Jan 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


University of Arizona

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Schaefer C. Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure . [Internet] [Masters thesis]. University of Arizona; 2017. [cited 2021 Jan 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

6. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Rodríguez Torrecillas, Ivan 1. Molecular basis to human P-glycoprotein reversion. [Internet] [Thesis]. Universitat Pompeu Fabra; 2015. [cited 2021 Jan 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

7. Perez, Jennifer. Évaluation de nouvelles thérapeutiques ciblées pour le traitement du chondrosarcome et de l'ostéosarcome : Evaluation of new therapeutic strategies for osteosarcoma and chondrosarcoma.

Degree: Docteur es, Biologie moléculaire, 2011, Université Claude Bernard – Lyon I

 <p>L'ostéosarcome et le chondrosarcome sont les tumeurs osseuses primitives les plus fréquentes. Ces tumeurs chimio- et radiorésistantes, sont extrêmement difficiles à traiter et le taux… (more)

Subjects/Keywords: Chimiorésistance; Ostéosarcome; Chondrosarcome; MTOR; Glycoprotéine P; Chemo-resistance; Osteosarcoma; Chondrosarcoma; MTOR; P-glycoprotein

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Perez, J. (2011). Évaluation de nouvelles thérapeutiques ciblées pour le traitement du chondrosarcome et de l'ostéosarcome : Evaluation of new therapeutic strategies for osteosarcoma and chondrosarcoma. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2011LYO10327

Chicago Manual of Style (16th Edition):

Perez, Jennifer. “Évaluation de nouvelles thérapeutiques ciblées pour le traitement du chondrosarcome et de l'ostéosarcome : Evaluation of new therapeutic strategies for osteosarcoma and chondrosarcoma.” 2011. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed January 22, 2021. http://www.theses.fr/2011LYO10327.

MLA Handbook (7th Edition):

Perez, Jennifer. “Évaluation de nouvelles thérapeutiques ciblées pour le traitement du chondrosarcome et de l'ostéosarcome : Evaluation of new therapeutic strategies for osteosarcoma and chondrosarcoma.” 2011. Web. 22 Jan 2021.

Vancouver:

Perez J. Évaluation de nouvelles thérapeutiques ciblées pour le traitement du chondrosarcome et de l'ostéosarcome : Evaluation of new therapeutic strategies for osteosarcoma and chondrosarcoma. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2011. [cited 2021 Jan 22]. Available from: http://www.theses.fr/2011LYO10327.

Council of Science Editors:

Perez J. Évaluation de nouvelles thérapeutiques ciblées pour le traitement du chondrosarcome et de l'ostéosarcome : Evaluation of new therapeutic strategies for osteosarcoma and chondrosarcoma. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2011. Available from: http://www.theses.fr/2011LYO10327

8. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Morgan AD. Quantitative Estimation of P-glycorptein-Mediated Drug Transport by Mechanistically Modeled Intrinsic Clearance. [Internet] [Thesis]. University of Western Ontario; 2015. [cited 2021 Jan 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. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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 Georgia

11. Cato, David Allen. Chemical synthesis of the O-linked oligosaccharide of P-Selectin Glycoprotein Ligand-1.

Degree: 2014, University of Georgia

P-Selectin Glycoprotein Ligand-1 (PSGL-1) is the key ligand for selectins involved in the inflammatory cascade. This glycoprotein is necessary for the initial steps of the… (more)

Subjects/Keywords: Inflammatory Cascade; Chronic Inflammation; P-Selectins; P-Selectin Glycoprotein Ligand-1; Leukocyte Transmigration

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cato, D. A. (2014). Chemical synthesis of the O-linked oligosaccharide of P-Selectin Glycoprotein Ligand-1. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/22609

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):

Cato, David Allen. “Chemical synthesis of the O-linked oligosaccharide of P-Selectin Glycoprotein Ligand-1.” 2014. Thesis, University of Georgia. Accessed January 22, 2021. http://hdl.handle.net/10724/22609.

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

MLA Handbook (7th Edition):

Cato, David Allen. “Chemical synthesis of the O-linked oligosaccharide of P-Selectin Glycoprotein Ligand-1.” 2014. Web. 22 Jan 2021.

Vancouver:

Cato DA. Chemical synthesis of the O-linked oligosaccharide of P-Selectin Glycoprotein Ligand-1. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/10724/22609.

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

Council of Science Editors:

Cato DA. Chemical synthesis of the O-linked oligosaccharide of P-Selectin Glycoprotein Ligand-1. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/22609

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


Dalhousie University

12. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. http://hdl.handle.net/10222/54084.

MLA Handbook (7th Edition):

Wang, Yan. “Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid.” 2014. Web. 22 Jan 2021.

Vancouver:

Wang Y. Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2021 Jan 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


Cornell University

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

Degree: PhD, Chemical Engineering, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery.” 2015. Doctoral Dissertation, Cornell University. Accessed January 22, 2021. http://hdl.handle.net/1813/41124.

MLA Handbook (7th Edition):

Crawford, Lindsey. “Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery.” 2015. Web. 22 Jan 2021.

Vancouver:

Crawford L. Exploitation Of P-Glycoprotein At The Blood Brain Barrier For Targeted Drug Delivery. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/1813/41124.

Council of Science Editors:

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


Lincoln University

14. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Bernardi GR. ABCB1 gene in Aporrectodea caliginosa - a potential ecotoxicological tool. [Internet] [Thesis]. Lincoln University; 2012. [cited 2021 Jan 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

15. Park, Soohyun. Development of Proteoliposome- and Nanowell-based Platforms to Assess P-glycoprotein Transport Activity.

Degree: 2016, Penn State University

 This thesis presents two platforms developed to assess transport activities of multidrug resistance (MDR) efflux pump, called P-glycoprotein (Pgp). Pgp is a transmembrane protein that… (more)

Subjects/Keywords: Giant liposome; P-glycoprotein; Multidrug resistance; Pore-spanning bilayer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Park, S. (2016). Development of Proteoliposome- and Nanowell-based Platforms to Assess P-glycoprotein Transport Activity. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13446szp164

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):

Park, Soohyun. “Development of Proteoliposome- and Nanowell-based Platforms to Assess P-glycoprotein Transport Activity.” 2016. Thesis, Penn State University. Accessed January 22, 2021. https://submit-etda.libraries.psu.edu/catalog/13446szp164.

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

MLA Handbook (7th Edition):

Park, Soohyun. “Development of Proteoliposome- and Nanowell-based Platforms to Assess P-glycoprotein Transport Activity.” 2016. Web. 22 Jan 2021.

Vancouver:

Park S. Development of Proteoliposome- and Nanowell-based Platforms to Assess P-glycoprotein Transport Activity. [Internet] [Thesis]. Penn State University; 2016. [cited 2021 Jan 22]. Available from: https://submit-etda.libraries.psu.edu/catalog/13446szp164.

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

Council of Science Editors:

Park S. Development of Proteoliposome- and Nanowell-based Platforms to Assess P-glycoprotein Transport Activity. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/13446szp164

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


Penn State University

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

Degree: 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

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):

Tan, Su-fern. “Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.” 2013. Thesis, Penn State University. Accessed January 22, 2021. https://submit-etda.libraries.psu.edu/catalog/19626.

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

MLA Handbook (7th Edition):

Tan, Su-fern. “Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia.” 2013. Web. 22 Jan 2021.

Vancouver:

Tan S. Role of Acid Ceramidase in Regulating Survival and Drug Resistance in Acute Myeloid Leukemia. [Internet] [Thesis]. Penn State University; 2013. [cited 2021 Jan 22]. Available from: https://submit-etda.libraries.psu.edu/catalog/19626.

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

Council of Science Editors:

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

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


University of Guelph

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

Degree: MS, Department of Molecular and Cellular Biology, 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

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. Masters Thesis, University of Guelph. Accessed January 22, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3196.

MLA Handbook (7th Edition):

Clay, Adam Thomas. “The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions.” 2011. Web. 22 Jan 2021.

Vancouver:

Clay AT. The Role of the Lipid Bilayer in P-glycoprotein Drug Binding, Transport and Catalytic Functions. [Internet] [Masters thesis]. University of Guelph; 2011. [cited 2021 Jan 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/3196.

Council of Science Editors:

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


University of Guelph

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

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

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

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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398

Chicago Manual of Style (16th Edition):

Vitsupakorn, Danoo. “Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter.” 2014. Masters Thesis, University of Guelph. Accessed January 22, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398.

MLA Handbook (7th Edition):

Vitsupakorn, Danoo. “Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter.” 2014. Web. 22 Jan 2021.

Vancouver:

Vitsupakorn D. Drug-drug interactions in the binding pocket of P-glycoprotein multidrug resistant transporter. [Internet] [Masters thesis]. University of Guelph; 2014. [cited 2021 Jan 22]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8398.

Council of Science Editors:

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


University of Adelaide

19. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Barratt DT. Pharmacogenomics of ABCB1 in maintenance pharmacotherapies for opioid dependence. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2021 Jan 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


University of Iowa

20. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Sheehy RM. Mechanisms of the anti-proliferative actions of the schweinfurthins in cancer cells. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2021 Jan 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


Univerzitet u Beogradu

21. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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


University of Manitoba

22. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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 Manchester

23. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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 January 22, 2021. 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 Jan 2021.

Vancouver:

Hamrang Z. The application of image analysis extensions to processes of relevance to drug development. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2021 Jan 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


University College Cork

24. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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 the Western Cape

25. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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 Jan 2021.

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 2021 Jan 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

26. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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. 22 Jan 2021.

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 2021 Jan 22]. 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

27. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Lam, Jessica Fung Chi. “Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions.” 2014. Doctoral Dissertation, University of Toronto. Accessed January 22, 2021. http://hdl.handle.net/1807/68430.

MLA Handbook (7th Edition):

Lam, Jessica Fung Chi. “Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions.” 2014. Web. 22 Jan 2021.

Vancouver:

Lam JFC. Risk Factors Associated With Opioid-Induced Toxicity: Ontogeny, Pharmacogenetics, and Drug Interactions. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2021 Jan 22]. 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

28. Sarah J Hemauer. Placental P-glycoprotein: Role in disposition of medications administered during pregnancy.

Degree: PhD, Human Biological Chemistry and Genetics, 2010, The University of Texas Medical Branch

 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hemauer, S. J. (2010). Placental P-glycoprotein: Role in disposition of medications administered during pregnancy. (Doctoral Dissertation). The University of Texas Medical Branch. Retrieved from http://hdl.handle.net/2152.3/142

Chicago Manual of Style (16th Edition):

Hemauer, Sarah J. “Placental P-glycoprotein: Role in disposition of medications administered during pregnancy.” 2010. Doctoral Dissertation, The University of Texas Medical Branch. Accessed January 22, 2021. http://hdl.handle.net/2152.3/142.

MLA Handbook (7th Edition):

Hemauer, Sarah J. “Placental P-glycoprotein: Role in disposition of medications administered during pregnancy.” 2010. Web. 22 Jan 2021.

Vancouver:

Hemauer SJ. Placental P-glycoprotein: Role in disposition of medications administered during pregnancy. [Internet] [Doctoral dissertation]. The University of Texas Medical Branch; 2010. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/2152.3/142.

Council of Science Editors:

Hemauer SJ. Placental P-glycoprotein: Role in disposition of medications administered during pregnancy. [Doctoral Dissertation]. The University of Texas Medical Branch; 2010. Available from: http://hdl.handle.net/2152.3/142


University of Arizona

29. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 January 22, 2021. 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. 22 Jan 2021.

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 2021 Jan 22]. 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 Georgia

30. Parvathaneni, Rajiv Krishna. Isolation, characterization and the dynamic structure of the pearl millet d2 dwarfing gene.

Degree: 2016, University of Georgia

 Pearl millet is one of the most important subsistence crops grown in India and sub-Saharan Africa. In many cereal crops, reduced height is a key… (more)

Subjects/Keywords: P-glycoprotein; comparative genomics; fine-mapping; haplotype analysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Parvathaneni, R. K. (2016). Isolation, characterization and the dynamic structure of the pearl millet d2 dwarfing gene. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/35440"

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):

Parvathaneni, Rajiv Krishna. “Isolation, characterization and the dynamic structure of the pearl millet d2 dwarfing gene.” 2016. Thesis, University of Georgia. Accessed January 22, 2021. http://hdl.handle.net/10724/35440".

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

MLA Handbook (7th Edition):

Parvathaneni, Rajiv Krishna. “Isolation, characterization and the dynamic structure of the pearl millet d2 dwarfing gene.” 2016. Web. 22 Jan 2021.

Vancouver:

Parvathaneni RK. Isolation, characterization and the dynamic structure of the pearl millet d2 dwarfing gene. [Internet] [Thesis]. University of Georgia; 2016. [cited 2021 Jan 22]. Available from: http://hdl.handle.net/10724/35440".

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

Council of Science Editors:

Parvathaneni RK. Isolation, characterization and the dynamic structure of the pearl millet d2 dwarfing gene. [Thesis]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/35440"

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

[1] [2] [3] [4] [5] [6] [7]

.