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Level: masters

You searched for subject:( P glycoprotein). Showing records 1 – 18 of 18 total matches.

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1. 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 26, 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. 26 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 26]. Available from: https://scholarworks.umass.edu/theses/424.

Council of Science Editors:

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


University of Arizona

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

Degree: 2017, University of Arizona

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Schaefer, Charles. “Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure .” 2017. Masters Thesis, University of Arizona. Accessed June 26, 2019. http://hdl.handle.net/10150/624091.

MLA Handbook (7th Edition):

Schaefer, Charles. “Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure .” 2017. Web. 26 Jun 2019.

Vancouver:

Schaefer C. Peripheral Inflammatory Pain and P-Glycoprotein in a Model of Chronic Opioid Exposure . [Internet] [Masters thesis]. University of Arizona; 2017. [cited 2019 Jun 26]. 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


Dalhousie University

3. 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 26, 2019. http://hdl.handle.net/10222/54084.

MLA Handbook (7th Edition):

Wang, Yan. “Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid.” 2014. Web. 26 Jun 2019.

Vancouver:

Wang Y. Surgery-induced inflammation reduces morphine distribution into cerebrospinal fluid. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2019 Jun 26]. 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 Manitoba

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

Degree: Pharmacology and Therapeutics, 2015, University of Manitoba

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

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

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APA (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 June 26, 2019. http://hdl.handle.net/1993/30206.

MLA Handbook (7th Edition):

Pogorzelec, Michael P J. “Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines.” 2015. Web. 26 Jun 2019.

Vancouver:

Pogorzelec MPJ. Protein kinase inhibitor effects on P-glycoprotein (P-gp) activity and expression in various cell lines. [Internet] [Masters thesis]. University of Manitoba; 2015. [cited 2019 Jun 26]. 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 Toronto

5. 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 26, 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. 26 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 26]. 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


University of Helsinki

6. Tepponen, Tuomas. MDR1-transportterin inhibition tutkiminen Sf9-MDR1-vesikkeleissä.

Degree: Farmaceutiska fakulteten, 2017, University of Helsinki

 <p>Multidrug resistance protein 1 (MDR1, p-glycoprotein) belongs to the ATP-binding cassette transporter family and it's encoded by ABCB1/MDR1 gene. It is a protein which transports… (more)

Subjects/Keywords: MDR1; p-glycoprotein; vesicle; transporter; N-methylquinidine; inhibitor; p-glykoproteiini; vesikkeli; transportteri; N-metyylikinidiini; inhibiittori; Biofarmaci; Biopharmacy; Biofarmasia; MDR1; p-glycoprotein; vesicle; transporter; N-methylquinidine; inhibitor; p-glykoproteiini; vesikkeli; transportteri; N-metyylikinidiini; inhibiittori

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APA (6th Edition):

Tepponen, T. (2017). MDR1-transportterin inhibition tutkiminen Sf9-MDR1-vesikkeleissä. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/230252

Chicago Manual of Style (16th Edition):

Tepponen, Tuomas. “MDR1-transportterin inhibition tutkiminen Sf9-MDR1-vesikkeleissä.” 2017. Masters Thesis, University of Helsinki. Accessed June 26, 2019. http://hdl.handle.net/10138/230252.

MLA Handbook (7th Edition):

Tepponen, Tuomas. “MDR1-transportterin inhibition tutkiminen Sf9-MDR1-vesikkeleissä.” 2017. Web. 26 Jun 2019.

Vancouver:

Tepponen T. MDR1-transportterin inhibition tutkiminen Sf9-MDR1-vesikkeleissä. [Internet] [Masters thesis]. University of Helsinki; 2017. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10138/230252.

Council of Science Editors:

Tepponen T. MDR1-transportterin inhibition tutkiminen Sf9-MDR1-vesikkeleissä. [Masters Thesis]. University of Helsinki; 2017. Available from: http://hdl.handle.net/10138/230252


University of Helsinki

7. Sjöstedt, Noora. Literature Review: Investigating Drug Transport at the Blood-Brain Barrier and the Effects of P-glycoprotein on the Brain Distribution of Drugs.

Degree: Farmaceutiska fakulteten, 2011, University of Helsinki

 The blood-brain barrier (BBB) is a unique barrier that strictly regulates the entry of endogenous substrates and xenobiotics into the brain. This is due to… (more)

Subjects/Keywords: blood-brain barrier (BBB); p-glycoprotein; pharmacokinetic (PK) modeling; efflux ratio (ER); p-glykoproteiini; farmakokineettinen (PK) mallitus; efluksisuhde (ER); veri-aivoeste; Biofarmaci; Biopharmacy; Biofarmasia; blood-brain barrier (BBB); p-glycoprotein; pharmacokinetic (PK) modeling; efflux ratio (ER); p-glykoproteiini; farmakokineettinen (PK) mallitus; efluksisuhde (ER); veri-aivoeste

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APA (6th Edition):

Sjöstedt, N. (2011). Literature Review: Investigating Drug Transport at the Blood-Brain Barrier and the Effects of P-glycoprotein on the Brain Distribution of Drugs. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/28695

Chicago Manual of Style (16th Edition):

Sjöstedt, Noora. “Literature Review: Investigating Drug Transport at the Blood-Brain Barrier and the Effects of P-glycoprotein on the Brain Distribution of Drugs.” 2011. Masters Thesis, University of Helsinki. Accessed June 26, 2019. http://hdl.handle.net/10138/28695.

MLA Handbook (7th Edition):

Sjöstedt, Noora. “Literature Review: Investigating Drug Transport at the Blood-Brain Barrier and the Effects of P-glycoprotein on the Brain Distribution of Drugs.” 2011. Web. 26 Jun 2019.

Vancouver:

Sjöstedt N. Literature Review: Investigating Drug Transport at the Blood-Brain Barrier and the Effects of P-glycoprotein on the Brain Distribution of Drugs. [Internet] [Masters thesis]. University of Helsinki; 2011. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10138/28695.

Council of Science Editors:

Sjöstedt N. Literature Review: Investigating Drug Transport at the Blood-Brain Barrier and the Effects of P-glycoprotein on the Brain Distribution of Drugs. [Masters Thesis]. University of Helsinki; 2011. Available from: http://hdl.handle.net/10138/28695


University of Pretoria

8. Durandt, Chrisna. Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans).

Degree: Immunology, 2006, University of Pretoria

The full text of this thesis/dissertation is not available online. Please <a href="mailto:[email protected]">contact us</a> if you need access. Read the abstract in the section 00front of this document. Advisors/Committee Members: Medlen, C.E. (advisor).

Subjects/Keywords: P-glycoprotein; Riminophenazines; Drug resistance; Membrane potential; Lipophilicity; UCTD

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APA (6th Edition):

Durandt, C. (2006). Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans). (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/27347

Chicago Manual of Style (16th Edition):

Durandt, Chrisna. “Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans).” 2006. Masters Thesis, University of Pretoria. Accessed June 26, 2019. http://hdl.handle.net/2263/27347.

MLA Handbook (7th Edition):

Durandt, Chrisna. “Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans).” 2006. Web. 26 Jun 2019.

Vancouver:

Durandt C. Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans). [Internet] [Masters thesis]. University of Pretoria; 2006. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/2263/27347.

Council of Science Editors:

Durandt C. Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans). [Masters Thesis]. University of Pretoria; 2006. Available from: http://hdl.handle.net/2263/27347


University of Pretoria

9. Durandt, Chrisna. Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans) .

Degree: 2006, University of Pretoria

The full text of this thesis/dissertation is not available online. Please <a href="mailto:[email protected]">contact us</a> if you need access. Read the abstract in the section 00front of this document. Advisors/Committee Members: Medlen, C.E (advisor).

Subjects/Keywords: P-glycoprotein; Riminophenazines; Drug resistance; Membrane potential; Lipophilicity; UCTD

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APA (6th Edition):

Durandt, C. (2006). Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans) . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-08182005-121909/

Chicago Manual of Style (16th Edition):

Durandt, Chrisna. “Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans) .” 2006. Masters Thesis, University of Pretoria. Accessed June 26, 2019. http://upetd.up.ac.za/thesis/available/etd-08182005-121909/.

MLA Handbook (7th Edition):

Durandt, Chrisna. “Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans) .” 2006. Web. 26 Jun 2019.

Vancouver:

Durandt C. Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans) . [Internet] [Masters thesis]. University of Pretoria; 2006. [cited 2019 Jun 26]. Available from: http://upetd.up.ac.za/thesis/available/etd-08182005-121909/.

Council of Science Editors:

Durandt C. Immuunregulerende, anti-mikrobiese en anti-tumor aktiwiteit van nuwe riminofenasiene (Afrikaans) . [Masters Thesis]. University of Pretoria; 2006. Available from: http://upetd.up.ac.za/thesis/available/etd-08182005-121909/


McGill University

10. Liu, Hao Yuan, 1961-. Genetic variation of a P-glycoprotein gene in unselected and ivermectin- and moxidectin-selected strains of Haemonchus contortus.

Degree: MS, Institute of Parasitology., 1998, McGill University

 Anthelmintics, antiparasitic agents, have been developed as a main weapon to control parasitic nematodes of domestic ruminants. Unfortunately, the intensive use of anthelmintics leads to… (more)

Subjects/Keywords: P-glycoprotein.; Ivermectin.; Haemonchus contortus.; Sheep  – Parasites.; Drug resistance.

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APA (6th Edition):

Liu, Hao Yuan, 1. (1998). Genetic variation of a P-glycoprotein gene in unselected and ivermectin- and moxidectin-selected strains of Haemonchus contortus. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile21597.pdf

Chicago Manual of Style (16th Edition):

Liu, Hao Yuan, 1961-. “Genetic variation of a P-glycoprotein gene in unselected and ivermectin- and moxidectin-selected strains of Haemonchus contortus.” 1998. Masters Thesis, McGill University. Accessed June 26, 2019. http://digitool.library.mcgill.ca/thesisfile21597.pdf.

MLA Handbook (7th Edition):

Liu, Hao Yuan, 1961-. “Genetic variation of a P-glycoprotein gene in unselected and ivermectin- and moxidectin-selected strains of Haemonchus contortus.” 1998. Web. 26 Jun 2019.

Vancouver:

Liu, Hao Yuan 1. Genetic variation of a P-glycoprotein gene in unselected and ivermectin- and moxidectin-selected strains of Haemonchus contortus. [Internet] [Masters thesis]. McGill University; 1998. [cited 2019 Jun 26]. Available from: http://digitool.library.mcgill.ca/thesisfile21597.pdf.

Council of Science Editors:

Liu, Hao Yuan 1. Genetic variation of a P-glycoprotein gene in unselected and ivermectin- and moxidectin-selected strains of Haemonchus contortus. [Masters Thesis]. McGill University; 1998. Available from: http://digitool.library.mcgill.ca/thesisfile21597.pdf


McGill University

11. Wang, Guanhua, 1970-. Genetic variation in P-glycoprotein in Haemonchus contortus following ivermectin selection.

Degree: MS, Institute of Parasitology., 2002, McGill University

 Resistance to ivermectin (IVM) in Haemonchus contortus has developed in many countries and its mechanism is still under investigation. P-glycoproteins (P-gp) are transmembrane proteins that… (more)

Subjects/Keywords: P-glycoprotein.; Haemonchus contortus.; Ivermectin.; Drug resistance.

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APA (6th Edition):

Wang, Guanhua, 1. (2002). Genetic variation in P-glycoprotein in Haemonchus contortus following ivermectin selection. (Masters Thesis). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile79203.pdf

Chicago Manual of Style (16th Edition):

Wang, Guanhua, 1970-. “Genetic variation in P-glycoprotein in Haemonchus contortus following ivermectin selection.” 2002. Masters Thesis, McGill University. Accessed June 26, 2019. http://digitool.library.mcgill.ca/thesisfile79203.pdf.

MLA Handbook (7th Edition):

Wang, Guanhua, 1970-. “Genetic variation in P-glycoprotein in Haemonchus contortus following ivermectin selection.” 2002. Web. 26 Jun 2019.

Vancouver:

Wang, Guanhua 1. Genetic variation in P-glycoprotein in Haemonchus contortus following ivermectin selection. [Internet] [Masters thesis]. McGill University; 2002. [cited 2019 Jun 26]. Available from: http://digitool.library.mcgill.ca/thesisfile79203.pdf.

Council of Science Editors:

Wang, Guanhua 1. Genetic variation in P-glycoprotein in Haemonchus contortus following ivermectin selection. [Masters Thesis]. McGill University; 2002. Available from: http://digitool.library.mcgill.ca/thesisfile79203.pdf


University of Toronto

12. Shi, Li. Repair of CFTR Defects Caused By Cystic Fibrosis Mutations.

Degree: 2013, University of Toronto

 <p>Cystic fibrosis is caused primarily by deletion of Phe508. An exciting discovery was that CFTR’s sister protein, the P-glycoprotein (P-gp) containing the equivalent mutation (ΔY490),… (more)

Subjects/Keywords: Biochemistry; cystic fibrosis; CFTR; membrane protein; chloride channel; P-glycoprotein; arginine mutagenesis; VX-809; 0307; 0566

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APA (6th Edition):

Shi, L. (2013). Repair of CFTR Defects Caused By Cystic Fibrosis Mutations. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42927

Chicago Manual of Style (16th Edition):

Shi, Li. “Repair of CFTR Defects Caused By Cystic Fibrosis Mutations.” 2013. Masters Thesis, University of Toronto. Accessed June 26, 2019. http://hdl.handle.net/1807/42927.

MLA Handbook (7th Edition):

Shi, Li. “Repair of CFTR Defects Caused By Cystic Fibrosis Mutations.” 2013. Web. 26 Jun 2019.

Vancouver:

Shi L. Repair of CFTR Defects Caused By Cystic Fibrosis Mutations. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/1807/42927.

Council of Science Editors:

Shi L. Repair of CFTR Defects Caused By Cystic Fibrosis Mutations. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42927

13. Romão, Carolina Martinez. Expressão da P-gp, MPR1 e LRP em células-tronco mesenquimais humanas derivadas do líquido amniótico e medula óssea.

Degree: Mestrado, Distúrbios do Crescimento Celular, Hemodinâmicos e da Hemostasia, 2012, University of São Paulo

 INTRODUÇÃO: O fenótipo de resistência a drogas é caracterizado pela superexpressão das proteínas da família ABC (ATP-Binding Cassette). A Pglicoproteína (P-gp), codificada pelo gene ABCB1,… (more)

Subjects/Keywords: Amniotic fluid; Bone marrow; Células-tronco mesenquimais; Drug resistance; Líquido amniótico; Medula óssea; Mesenchymal stem cells; P-glicoproteína; P-glycoprotein; Resistência a medicamentos

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APA (6th Edition):

Romão, C. M. (2012). Expressão da P-gp, MPR1 e LRP em células-tronco mesenquimais humanas derivadas do líquido amniótico e medula óssea. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5167/tde-27072012-154244/ ;

Chicago Manual of Style (16th Edition):

Romão, Carolina Martinez. “Expressão da P-gp, MPR1 e LRP em células-tronco mesenquimais humanas derivadas do líquido amniótico e medula óssea.” 2012. Masters Thesis, University of São Paulo. Accessed June 26, 2019. http://www.teses.usp.br/teses/disponiveis/5/5167/tde-27072012-154244/ ;.

MLA Handbook (7th Edition):

Romão, Carolina Martinez. “Expressão da P-gp, MPR1 e LRP em células-tronco mesenquimais humanas derivadas do líquido amniótico e medula óssea.” 2012. Web. 26 Jun 2019.

Vancouver:

Romão CM. Expressão da P-gp, MPR1 e LRP em células-tronco mesenquimais humanas derivadas do líquido amniótico e medula óssea. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2019 Jun 26]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5167/tde-27072012-154244/ ;.

Council of Science Editors:

Romão CM. Expressão da P-gp, MPR1 e LRP em células-tronco mesenquimais humanas derivadas do líquido amniótico e medula óssea. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/5/5167/tde-27072012-154244/ ;

14. Souza, Pamela Oliveira de. Polimorfismos de enzimas de fase 1 e 2 do metabolismo de drogas em pacientes portadores de linfoma difuso de grandes células B.

Degree: Mestrado, Distúrbios do Crescimento Celular, Hemodinâmicos e da Hemostasia, 2011, University of São Paulo

 <p>Para avaliar a influência dos polimorfismos de nucleotídeo único (SNPs) do CYP2B6, CYP3A5, GSTM1, GSTP1, GSTT1, PON1, NQO1 e MDR1 na resposta ao tratamento com… (more)

Subjects/Keywords: Diffuse large B-cell lymphoma; Enzymes polymorphisms; Farmacogenética; Genes MDR; Genes MDR; Glicoproteina P; Linfoma difuso de grandes células B; P-glycoprotein; Pharmacogenetics; Polimorfismos de enzimas; Polimorfismos de nucleotídeo único; Single nucleotide polymorphisms

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APA (6th Edition):

Souza, P. O. d. (2011). Polimorfismos de enzimas de fase 1 e 2 do metabolismo de drogas em pacientes portadores de linfoma difuso de grandes células B. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5167/tde-22072011-140320/ ;

Chicago Manual of Style (16th Edition):

Souza, Pamela Oliveira de. “Polimorfismos de enzimas de fase 1 e 2 do metabolismo de drogas em pacientes portadores de linfoma difuso de grandes células B.” 2011. Masters Thesis, University of São Paulo. Accessed June 26, 2019. http://www.teses.usp.br/teses/disponiveis/5/5167/tde-22072011-140320/ ;.

MLA Handbook (7th Edition):

Souza, Pamela Oliveira de. “Polimorfismos de enzimas de fase 1 e 2 do metabolismo de drogas em pacientes portadores de linfoma difuso de grandes células B.” 2011. Web. 26 Jun 2019.

Vancouver:

Souza POd. Polimorfismos de enzimas de fase 1 e 2 do metabolismo de drogas em pacientes portadores de linfoma difuso de grandes células B. [Internet] [Masters thesis]. University of São Paulo; 2011. [cited 2019 Jun 26]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5167/tde-22072011-140320/ ;.

Council of Science Editors:

Souza POd. Polimorfismos de enzimas de fase 1 e 2 do metabolismo de drogas em pacientes portadores de linfoma difuso de grandes células B. [Masters Thesis]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/5/5167/tde-22072011-140320/ ;

15. Koegle, Eric Richard. Determining the Intracellular Localization and Efficacy of Novel Anticancer Agents in Human Breast Cancer Cell Lines Through the Use of Fluorescent Microscopy.

Degree: MSin Pharmaceutical Sciences, Pharmaceutical Science, 2008, University of Toledo

 Breast cancer is the second most frequently diagnosed cancer and it ranks second among cancer deaths in women. The anthracycline antibiotic doxorubicin, more commonly known… (more)

Subjects/Keywords: Cellular Biology; Oncology; Pharmaceuticals; Pharmacology; Toxicology; Breast Cancer; Topoisomerase II; MCF-7; BBR3378; BBR3409; P-glycoprotein

…resistant is through the increased expression of a 170-kDa membrane glycoprotein called P… …amine side arms, therefore, it is not cross resistant in P-glycoprotein expressing cells… …compound in cells over expressing P-glycoprotein. The compound BBR3409 is structurally similar… …distribution of these two drugs in both the wild-type MCF-7 and the P-glycoprotein over expressing… …the drug to localize into distinct cytoplasmic vesicles in both wild type and P-gp… 

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

APA (6th Edition):

Koegle, E. R. (2008). Determining the Intracellular Localization and Efficacy of Novel Anticancer Agents in Human Breast Cancer Cell Lines Through the Use of Fluorescent Microscopy. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1234749487

Chicago Manual of Style (16th Edition):

Koegle, Eric Richard. “Determining the Intracellular Localization and Efficacy of Novel Anticancer Agents in Human Breast Cancer Cell Lines Through the Use of Fluorescent Microscopy.” 2008. Masters Thesis, University of Toledo. Accessed June 26, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1234749487.

MLA Handbook (7th Edition):

Koegle, Eric Richard. “Determining the Intracellular Localization and Efficacy of Novel Anticancer Agents in Human Breast Cancer Cell Lines Through the Use of Fluorescent Microscopy.” 2008. Web. 26 Jun 2019.

Vancouver:

Koegle ER. Determining the Intracellular Localization and Efficacy of Novel Anticancer Agents in Human Breast Cancer Cell Lines Through the Use of Fluorescent Microscopy. [Internet] [Masters thesis]. University of Toledo; 2008. [cited 2019 Jun 26]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1234749487.

Council of Science Editors:

Koegle ER. Determining the Intracellular Localization and Efficacy of Novel Anticancer Agents in Human Breast Cancer Cell Lines Through the Use of Fluorescent Microscopy. [Masters Thesis]. University of Toledo; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1234749487

16. Ellis, Kelstan Lynch. THE EFFECTS OF HIV INFECTION ON THE EXPRESSION OF THE DRUG EFFLUX PROTEINS P-GLYCOPROTEIN AND BREAST CANCER RESISTANCE PROTEIN IN A HUMAN INTESTINE MODEL.

Degree: MS, Preventive Medicine and Public Health, 2012, University of Kansas

 Background: Emerging evidence suggests poor antiretroviral penetration within human gastrointestinal (GI) tissues may contribute to HIV persistence within reservoirs despite effective therapy. We hypothesize that… (more)

Subjects/Keywords: Pharmacology; Biology; Bcrp; Drug efflux pumps; Gi tract; Hiv; P-glycoprotein; Viral reservoirs

…of P-glycoprotein and BCRP .. ….. ….. ….. . Table 2 – Summary of Primary and… …of P-glycoprotein Expression in Primary Lymphocytes in Response to Exposure with HIV… …Figure 6 – Representative Blot of P-glycoprotein and BCRP Expression Caco2 Cells Exposed to HIV… …Figure 7 – Analysis of P-glycoprotein Expression in Caco2 Cells in Response to Exposure with… …Exposure with HIV ….. ….. ….. Figure 9 – Exposure to Tat increases P-glycoprotein… 

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

APA (6th Edition):

Ellis, K. L. (2012). THE EFFECTS OF HIV INFECTION ON THE EXPRESSION OF THE DRUG EFFLUX PROTEINS P-GLYCOPROTEIN AND BREAST CANCER RESISTANCE PROTEIN IN A HUMAN INTESTINE MODEL. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/10240

Chicago Manual of Style (16th Edition):

Ellis, Kelstan Lynch. “THE EFFECTS OF HIV INFECTION ON THE EXPRESSION OF THE DRUG EFFLUX PROTEINS P-GLYCOPROTEIN AND BREAST CANCER RESISTANCE PROTEIN IN A HUMAN INTESTINE MODEL.” 2012. Masters Thesis, University of Kansas. Accessed June 26, 2019. http://hdl.handle.net/1808/10240.

MLA Handbook (7th Edition):

Ellis, Kelstan Lynch. “THE EFFECTS OF HIV INFECTION ON THE EXPRESSION OF THE DRUG EFFLUX PROTEINS P-GLYCOPROTEIN AND BREAST CANCER RESISTANCE PROTEIN IN A HUMAN INTESTINE MODEL.” 2012. Web. 26 Jun 2019.

Vancouver:

Ellis KL. THE EFFECTS OF HIV INFECTION ON THE EXPRESSION OF THE DRUG EFFLUX PROTEINS P-GLYCOPROTEIN AND BREAST CANCER RESISTANCE PROTEIN IN A HUMAN INTESTINE MODEL. [Internet] [Masters thesis]. University of Kansas; 2012. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/1808/10240.

Council of Science Editors:

Ellis KL. THE EFFECTS OF HIV INFECTION ON THE EXPRESSION OF THE DRUG EFFLUX PROTEINS P-GLYCOPROTEIN AND BREAST CANCER RESISTANCE PROTEIN IN A HUMAN INTESTINE MODEL. [Masters Thesis]. University of Kansas; 2012. Available from: http://hdl.handle.net/1808/10240

17. Suvanto, Satu. P-glycoprotein characteristics and investigation of P-glycoprotein mediated drug-drug interactions with in vitro methods.

Degree: Farmaceutiska fakulteten, 2014, University of Helsinki

 <p>P-glycoprotein is an ATP-dependent efflux protein expressed in many tissues which participate in absorption, distribution and elimination of drug molecules. It can mediate clinically significant… (more)

Subjects/Keywords: MDRI; MDCKII-MDR1; P-glycoprotein/MDRI; transporter; membrane vesicles; drug-drug; P-glykoproteiini; kuljetusproteiini; membraani vesikkelit; lääke-lääke yhteisvaikutus; Biofarmaci; Biopharmacy; Biofarmasia; MDRI; MDCKII-MDR1; P-glycoprotein/MDRI; transporter; membrane vesicles; drug-drug; P-glykoproteiini; kuljetusproteiini; membraani vesikkelit; lääke-lääke yhteisvaikutus

…STRUCTURAL CHARACTERISTICS OF P-GLYCOPROTEIN 2.1 Structure of P-glycoprotein Human P-gp is a… …cell. Figure 2. P-glycoprotein is located in the cell membrane with ATP (adenosine… …structure of mouse P-glycoprotein binding cavity hosting a P-gp inhibitor QZ59-RRR A) from… …gp can host two molecules of a P-glycoprotein substrate QZ59-SSS at the same time in the… …and transport function. 9 Figure 6. P-glycoprotein has two binding sites (H- and R… 

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APA (6th Edition):

Suvanto, S. (2014). P-glycoprotein characteristics and investigation of P-glycoprotein mediated drug-drug interactions with in vitro methods. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/44691

Chicago Manual of Style (16th Edition):

Suvanto, Satu. “P-glycoprotein characteristics and investigation of P-glycoprotein mediated drug-drug interactions with in vitro methods.” 2014. Masters Thesis, University of Helsinki. Accessed June 26, 2019. http://hdl.handle.net/10138/44691.

MLA Handbook (7th Edition):

Suvanto, Satu. “P-glycoprotein characteristics and investigation of P-glycoprotein mediated drug-drug interactions with in vitro methods.” 2014. Web. 26 Jun 2019.

Vancouver:

Suvanto S. P-glycoprotein characteristics and investigation of P-glycoprotein mediated drug-drug interactions with in vitro methods. [Internet] [Masters thesis]. University of Helsinki; 2014. [cited 2019 Jun 26]. Available from: http://hdl.handle.net/10138/44691.

Council of Science Editors:

Suvanto S. P-glycoprotein characteristics and investigation of P-glycoprotein mediated drug-drug interactions with in vitro methods. [Masters Thesis]. University of Helsinki; 2014. Available from: http://hdl.handle.net/10138/44691

18. Abadi, Marcia Datz. "Análise imunohistoquímica do osteossarcoma em pacientes com e sem metástases e sua correlação prognóstica".

Degree: Mestrado, Ortopedia e Traumatologia, 2005, University of São Paulo

 <p>As proteínas p53, MDM-2, c-Kit, ErbB-2, PCNA e p-glicoproteína foram estudadas em 42 amostras de osteossarcoma ao diagnóstico, através da técnica de imunohistoquímica, e foram… (more)

Subjects/Keywords: ANTÍGENO NUCLEAR DE CÉLULA EM PROLIFERAÇÃO; GLICOPROTEÍNA P; IMMUNOHISTOCHEMISTRY/methods; IMUNOHISTOQUÍMICA/métodos; OSTEOSARCOMA/pathology; OSTEOSARCOMA/patologia; P-GLYCOPROTEIN; PROGNOSIS; PROGNÓSTICO; PROLIFERATING CELL NUCLEAR ANTIGEN; PROTEIN p53; PROTEÍNA P53; PROTEÍNA PROTO-ONCOGÊNICA C-KIT; PROTO-ONCOGENE PROTEIN C-KIT; RECEPTOR ERBB-2; RECEPTOR ERBB-2

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

APA (6th Edition):

Abadi, M. D. (2005). "Análise imunohistoquímica do osteossarcoma em pacientes com e sem metástases e sua correlação prognóstica". (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5140/tde-17022006-132205/ ;

Chicago Manual of Style (16th Edition):

Abadi, Marcia Datz. “"Análise imunohistoquímica do osteossarcoma em pacientes com e sem metástases e sua correlação prognóstica".” 2005. Masters Thesis, University of São Paulo. Accessed June 26, 2019. http://www.teses.usp.br/teses/disponiveis/5/5140/tde-17022006-132205/ ;.

MLA Handbook (7th Edition):

Abadi, Marcia Datz. “"Análise imunohistoquímica do osteossarcoma em pacientes com e sem metástases e sua correlação prognóstica".” 2005. Web. 26 Jun 2019.

Vancouver:

Abadi MD. "Análise imunohistoquímica do osteossarcoma em pacientes com e sem metástases e sua correlação prognóstica". [Internet] [Masters thesis]. University of São Paulo; 2005. [cited 2019 Jun 26]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5140/tde-17022006-132205/ ;.

Council of Science Editors:

Abadi MD. "Análise imunohistoquímica do osteossarcoma em pacientes com e sem metástases e sua correlação prognóstica". [Masters Thesis]. University of São Paulo; 2005. Available from: http://www.teses.usp.br/teses/disponiveis/5/5140/tde-17022006-132205/ ;

.