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You searched for subject:(Multidrug Resistance Protein 4). Showing records 1 – 30 of 42626 total matches.

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Queens University

1. Miah, Mohammad Fahad. Investigations into the Plasma Membrane Trafficking of Multidrug Resistance Protein 4 (ABCC4/MRP4) .

Degree: Pathology and Molecular Medicine, 2015, Queens University

Multidrug resistance protein 4 (MRP4) is a member of subfamily C of the ATP-binding cassette superfamily of membrane transport proteins. In polarized cells, MRP4 localizes… (more)

Subjects/Keywords: Multidrug Resistance Protein 4 ; Membrane Protein Trafficking

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

APA (6th Edition):

Miah, M. F. (2015). Investigations into the Plasma Membrane Trafficking of Multidrug Resistance Protein 4 (ABCC4/MRP4) . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13589

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):

Miah, Mohammad Fahad. “Investigations into the Plasma Membrane Trafficking of Multidrug Resistance Protein 4 (ABCC4/MRP4) .” 2015. Thesis, Queens University. Accessed April 15, 2021. http://hdl.handle.net/1974/13589.

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

MLA Handbook (7th Edition):

Miah, Mohammad Fahad. “Investigations into the Plasma Membrane Trafficking of Multidrug Resistance Protein 4 (ABCC4/MRP4) .” 2015. Web. 15 Apr 2021.

Vancouver:

Miah MF. Investigations into the Plasma Membrane Trafficking of Multidrug Resistance Protein 4 (ABCC4/MRP4) . [Internet] [Thesis]. Queens University; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1974/13589.

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

Council of Science Editors:

Miah MF. Investigations into the Plasma Membrane Trafficking of Multidrug Resistance Protein 4 (ABCC4/MRP4) . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13589

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


Texas State University – San Marcos

2. Freeman, Kris Ray. Proteomic Comparison Between Mrp4 Knockout and Wild Type Mouse Brain, Liver, Kidney and Serum.

Degree: MS, Biology, 2013, Texas State University – San Marcos

Multidrug resistance protein 4 (MRP4) is a transmembrane efflux protein capable of substrate-specific transport of endogenous and xenobiotic molecules across the cell membrane, including several… (more)

Subjects/Keywords: MRP4; Multidrug Resistance Protein 4; Proteomic; Knockout; Biomarkers; Inflammation

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APA (6th Edition):

Freeman, K. R. (2013). Proteomic Comparison Between Mrp4 Knockout and Wild Type Mouse Brain, Liver, Kidney and Serum. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/6336

Chicago Manual of Style (16th Edition):

Freeman, Kris Ray. “Proteomic Comparison Between Mrp4 Knockout and Wild Type Mouse Brain, Liver, Kidney and Serum.” 2013. Masters Thesis, Texas State University – San Marcos. Accessed April 15, 2021. https://digital.library.txstate.edu/handle/10877/6336.

MLA Handbook (7th Edition):

Freeman, Kris Ray. “Proteomic Comparison Between Mrp4 Knockout and Wild Type Mouse Brain, Liver, Kidney and Serum.” 2013. Web. 15 Apr 2021.

Vancouver:

Freeman KR. Proteomic Comparison Between Mrp4 Knockout and Wild Type Mouse Brain, Liver, Kidney and Serum. [Internet] [Masters thesis]. Texas State University – San Marcos; 2013. [cited 2021 Apr 15]. Available from: https://digital.library.txstate.edu/handle/10877/6336.

Council of Science Editors:

Freeman KR. Proteomic Comparison Between Mrp4 Knockout and Wild Type Mouse Brain, Liver, Kidney and Serum. [Masters Thesis]. Texas State University – San Marcos; 2013. Available from: https://digital.library.txstate.edu/handle/10877/6336

3. Carillion, Aude. Physiopathologie de la dysfonction bêta-adrénergique et rôle de la protéine MRP4 au cours du vieillissement, du diabète et du syndrome métabolique : Physiopathology of beta-adrenergic dysfunction and role of MRP4 during aging, diabetes mellitus and metabolic syndrom.

Degree: Docteur es, Physiologie et Physiopathologie, 2015, Université Pierre et Marie Curie – Paris VI

Les travaux présentés dans ce mémoire ont pour objectif d’approfondir la compréhension de l’altération de la réponse à la stimulation des récepteurs β-adrénergiques dans plusieurs… (more)

Subjects/Keywords: Stimulation β-adrénergique; Sénescente; Cardiopathie diabétique; Syndrome métabolique; Multidrug resistance associated protein 4; MRP4; Βeta-adrenergic stimulation; Aging; 572.4

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APA (6th Edition):

Carillion, A. (2015). Physiopathologie de la dysfonction bêta-adrénergique et rôle de la protéine MRP4 au cours du vieillissement, du diabète et du syndrome métabolique : Physiopathology of beta-adrenergic dysfunction and role of MRP4 during aging, diabetes mellitus and metabolic syndrom. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2015PA066485

Chicago Manual of Style (16th Edition):

Carillion, Aude. “Physiopathologie de la dysfonction bêta-adrénergique et rôle de la protéine MRP4 au cours du vieillissement, du diabète et du syndrome métabolique : Physiopathology of beta-adrenergic dysfunction and role of MRP4 during aging, diabetes mellitus and metabolic syndrom.” 2015. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed April 15, 2021. http://www.theses.fr/2015PA066485.

MLA Handbook (7th Edition):

Carillion, Aude. “Physiopathologie de la dysfonction bêta-adrénergique et rôle de la protéine MRP4 au cours du vieillissement, du diabète et du syndrome métabolique : Physiopathology of beta-adrenergic dysfunction and role of MRP4 during aging, diabetes mellitus and metabolic syndrom.” 2015. Web. 15 Apr 2021.

Vancouver:

Carillion A. Physiopathologie de la dysfonction bêta-adrénergique et rôle de la protéine MRP4 au cours du vieillissement, du diabète et du syndrome métabolique : Physiopathology of beta-adrenergic dysfunction and role of MRP4 during aging, diabetes mellitus and metabolic syndrom. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2015PA066485.

Council of Science Editors:

Carillion A. Physiopathologie de la dysfonction bêta-adrénergique et rôle de la protéine MRP4 au cours du vieillissement, du diabète et du syndrome métabolique : Physiopathology of beta-adrenergic dysfunction and role of MRP4 during aging, diabetes mellitus and metabolic syndrom. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. Available from: http://www.theses.fr/2015PA066485


Queens University

4. Slot, Andrew Johannes. Modulation of Human Multidrug Resistance Proteins by Reactive Quinone-based Glutathione Conjugates .

Degree: Pathology and Molecular Medicine, 2015, Queens University

 The multidrug resistance protein 1 (MRP1) and MRP2 mediate the ATP-dependent cellular efflux of a diverse set of organic molecules including many glutathione (GSH) conjugates.… (more)

Subjects/Keywords: Multidrug Resistance Protein ; Glutathione ; Quinone ; Conjugate

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APA (6th Edition):

Slot, A. J. (2015). Modulation of Human Multidrug Resistance Proteins by Reactive Quinone-based Glutathione Conjugates . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/12748

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):

Slot, Andrew Johannes. “Modulation of Human Multidrug Resistance Proteins by Reactive Quinone-based Glutathione Conjugates .” 2015. Thesis, Queens University. Accessed April 15, 2021. http://hdl.handle.net/1974/12748.

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

MLA Handbook (7th Edition):

Slot, Andrew Johannes. “Modulation of Human Multidrug Resistance Proteins by Reactive Quinone-based Glutathione Conjugates .” 2015. Web. 15 Apr 2021.

Vancouver:

Slot AJ. Modulation of Human Multidrug Resistance Proteins by Reactive Quinone-based Glutathione Conjugates . [Internet] [Thesis]. Queens University; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1974/12748.

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

Council of Science Editors:

Slot AJ. Modulation of Human Multidrug Resistance Proteins by Reactive Quinone-based Glutathione Conjugates . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/12748

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


University of Manitoba

5. Wang, Jie. Fibroblast growth factor-16 and acute doxorubicin cardiotoxicity: a target for early protection.

Degree: Physiology and Pathophysiology, 2018, University of Manitoba

 Background: Doxorubicin is an anti-cancer drug that is widely used in chemotherapy. However, doxorubicin-induced cardiotoxicity is a major risk factor for cancer patients and survivors,… (more)

Subjects/Keywords: Fibroblast growth factor 16; doxorubicin; multidrug resistance protein 1; cardioprotection

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APA (6th Edition):

Wang, J. (2018). Fibroblast growth factor-16 and acute doxorubicin cardiotoxicity: a target for early protection. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/33048

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):

Wang, Jie. “Fibroblast growth factor-16 and acute doxorubicin cardiotoxicity: a target for early protection.” 2018. Thesis, University of Manitoba. Accessed April 15, 2021. http://hdl.handle.net/1993/33048.

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

MLA Handbook (7th Edition):

Wang, Jie. “Fibroblast growth factor-16 and acute doxorubicin cardiotoxicity: a target for early protection.” 2018. Web. 15 Apr 2021.

Vancouver:

Wang J. Fibroblast growth factor-16 and acute doxorubicin cardiotoxicity: a target for early protection. [Internet] [Thesis]. University of Manitoba; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1993/33048.

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

Council of Science Editors:

Wang J. Fibroblast growth factor-16 and acute doxorubicin cardiotoxicity: a target for early protection. [Thesis]. University of Manitoba; 2018. Available from: http://hdl.handle.net/1993/33048

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


Queens University

6. Wang, Xiaoqian. Biochemical Characterization of Nucleotide and Protein Interactions of Human Multidrug Resistance Protein 1 (MRP1/ABCC1) .

Degree: Pathology and Molecular Medicine, 2008, Queens University

Multidrug resistance protein 1 (MRP1) is an integral membrane protein belonging to the ATP-binding cassette (ABC) superfamily that utilizes ATP binding and hydrolysis to transport… (more)

Subjects/Keywords: protein interaction ; multidrug resistance

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APA (6th Edition):

Wang, X. (2008). Biochemical Characterization of Nucleotide and Protein Interactions of Human Multidrug Resistance Protein 1 (MRP1/ABCC1) . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/1610

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):

Wang, Xiaoqian. “Biochemical Characterization of Nucleotide and Protein Interactions of Human Multidrug Resistance Protein 1 (MRP1/ABCC1) .” 2008. Thesis, Queens University. Accessed April 15, 2021. http://hdl.handle.net/1974/1610.

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

MLA Handbook (7th Edition):

Wang, Xiaoqian. “Biochemical Characterization of Nucleotide and Protein Interactions of Human Multidrug Resistance Protein 1 (MRP1/ABCC1) .” 2008. Web. 15 Apr 2021.

Vancouver:

Wang X. Biochemical Characterization of Nucleotide and Protein Interactions of Human Multidrug Resistance Protein 1 (MRP1/ABCC1) . [Internet] [Thesis]. Queens University; 2008. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1974/1610.

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

Council of Science Editors:

Wang X. Biochemical Characterization of Nucleotide and Protein Interactions of Human Multidrug Resistance Protein 1 (MRP1/ABCC1) . [Thesis]. Queens University; 2008. Available from: http://hdl.handle.net/1974/1610

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


University of Ottawa

7. Rainey, Jenna. The Regulation of Multidrug Resistance Phosphoglycoprotein (MDR1/P-gp) and Breast Cancer Resistance Protein (BCRP) in the Human Placenta .

Degree: 2011, University of Ottawa

Multidrug resistance phosphoglycoprotein (MDR1/P-gp) and breast cancer resistance protein (BCRP) were first isolated in chemoresistant cancer cells and have since been found in a variety… (more)

Subjects/Keywords: Multidrug Resistance Phosphoglycoprotein (MDR1/P-gp); Breast Cancer Resistance Protein (BCRP); Human Placenta

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APA (6th Edition):

Rainey, J. (2011). The Regulation of Multidrug Resistance Phosphoglycoprotein (MDR1/P-gp) and Breast Cancer Resistance Protein (BCRP) in the Human Placenta . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/19961

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):

Rainey, Jenna. “The Regulation of Multidrug Resistance Phosphoglycoprotein (MDR1/P-gp) and Breast Cancer Resistance Protein (BCRP) in the Human Placenta .” 2011. Thesis, University of Ottawa. Accessed April 15, 2021. http://hdl.handle.net/10393/19961.

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

MLA Handbook (7th Edition):

Rainey, Jenna. “The Regulation of Multidrug Resistance Phosphoglycoprotein (MDR1/P-gp) and Breast Cancer Resistance Protein (BCRP) in the Human Placenta .” 2011. Web. 15 Apr 2021.

Vancouver:

Rainey J. The Regulation of Multidrug Resistance Phosphoglycoprotein (MDR1/P-gp) and Breast Cancer Resistance Protein (BCRP) in the Human Placenta . [Internet] [Thesis]. University of Ottawa; 2011. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10393/19961.

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

Council of Science Editors:

Rainey J. The Regulation of Multidrug Resistance Phosphoglycoprotein (MDR1/P-gp) and Breast Cancer Resistance Protein (BCRP) in the Human Placenta . [Thesis]. University of Ottawa; 2011. Available from: http://hdl.handle.net/10393/19961

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


University of Kentucky

8. Ye, Cui. STABILITY STUDIES OF MEMBRANE PROTEINS.

Degree: 2014, University of Kentucky

 The World Health Organization has identified antimicrobial resistance as one of the top three threats to human health. Gram-negative bacteria such as Escherichia coli are… (more)

Subjects/Keywords: Multidrug resistance; multidrug efflux pump; outer membrane proteins; protein stability; AcrB; Biochemistry; Molecular Biology; Structural Biology

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APA (6th Edition):

Ye, C. (2014). STABILITY STUDIES OF MEMBRANE PROTEINS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/chemistry_etds/33

Chicago Manual of Style (16th Edition):

Ye, Cui. “STABILITY STUDIES OF MEMBRANE PROTEINS.” 2014. Doctoral Dissertation, University of Kentucky. Accessed April 15, 2021. https://uknowledge.uky.edu/chemistry_etds/33.

MLA Handbook (7th Edition):

Ye, Cui. “STABILITY STUDIES OF MEMBRANE PROTEINS.” 2014. Web. 15 Apr 2021.

Vancouver:

Ye C. STABILITY STUDIES OF MEMBRANE PROTEINS. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2021 Apr 15]. Available from: https://uknowledge.uky.edu/chemistry_etds/33.

Council of Science Editors:

Ye C. STABILITY STUDIES OF MEMBRANE PROTEINS. [Doctoral Dissertation]. University of Kentucky; 2014. Available from: https://uknowledge.uky.edu/chemistry_etds/33


Rutgers University

9. Udasin, Ronald G., 1987-. Resistance to vesicant injury by efflux transporters.

Degree: PhD, Toxicology, 2015, Rutgers University

Sulfur mustard and nitrogen mustard (mechlorethamine, HN2) are potent vesicants used in chemical warfare and cancer chemotherapy that primarily target skin, eye, and lung. These… (more)

Subjects/Keywords: Multidrug resistance; Chemotherapy

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APA (6th Edition):

Udasin, Ronald G., 1. (2015). Resistance to vesicant injury by efflux transporters. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/48705/

Chicago Manual of Style (16th Edition):

Udasin, Ronald G., 1987-. “Resistance to vesicant injury by efflux transporters.” 2015. Doctoral Dissertation, Rutgers University. Accessed April 15, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/48705/.

MLA Handbook (7th Edition):

Udasin, Ronald G., 1987-. “Resistance to vesicant injury by efflux transporters.” 2015. Web. 15 Apr 2021.

Vancouver:

Udasin, Ronald G. 1. Resistance to vesicant injury by efflux transporters. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2021 Apr 15]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48705/.

Council of Science Editors:

Udasin, Ronald G. 1. Resistance to vesicant injury by efflux transporters. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/48705/


University of Tennessee – Knoxville

10. Samuels, Ronita. An Epidemiologic Study of Antimicrobial Resistance.

Degree: 2019, University of Tennessee – Knoxville

 The emergence of antimicrobial resistant bacteria has become a serious public health concern. The use of antimicrobials for prophylaxis make it important to estimate the… (more)

Subjects/Keywords: Antimicrobial Resistance; multidrug resistance; Staphylococcus

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APA (6th Edition):

Samuels, R. (2019). An Epidemiologic Study of Antimicrobial Resistance. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/5703

Chicago Manual of Style (16th Edition):

Samuels, Ronita. “An Epidemiologic Study of Antimicrobial Resistance.” 2019. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed April 15, 2021. https://trace.tennessee.edu/utk_graddiss/5703.

MLA Handbook (7th Edition):

Samuels, Ronita. “An Epidemiologic Study of Antimicrobial Resistance.” 2019. Web. 15 Apr 2021.

Vancouver:

Samuels R. An Epidemiologic Study of Antimicrobial Resistance. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2019. [cited 2021 Apr 15]. Available from: https://trace.tennessee.edu/utk_graddiss/5703.

Council of Science Editors:

Samuels R. An Epidemiologic Study of Antimicrobial Resistance. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2019. Available from: https://trace.tennessee.edu/utk_graddiss/5703

11. Delmar, Jared Armand. A structural biology approach to the problem of antibiotic resistance in bacteria.

Degree: 2017, Iowa State University

 X-ray crystallography remains the most robust method to determine protein structure at the atomic level. We demonstrate how these structural studies can directly contribute to… (more)

Subjects/Keywords: Antimicrobial efflux; Chloroplast cell division; Membrane protein crystallization; Multidrug resistance; Xray crystallography; Biochemistry; Molecular Biology

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APA (6th Edition):

Delmar, J. A. (2017). A structural biology approach to the problem of antibiotic resistance in bacteria. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/15291

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):

Delmar, Jared Armand. “A structural biology approach to the problem of antibiotic resistance in bacteria.” 2017. Thesis, Iowa State University. Accessed April 15, 2021. https://lib.dr.iastate.edu/etd/15291.

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

MLA Handbook (7th Edition):

Delmar, Jared Armand. “A structural biology approach to the problem of antibiotic resistance in bacteria.” 2017. Web. 15 Apr 2021.

Vancouver:

Delmar JA. A structural biology approach to the problem of antibiotic resistance in bacteria. [Internet] [Thesis]. Iowa State University; 2017. [cited 2021 Apr 15]. Available from: https://lib.dr.iastate.edu/etd/15291.

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

Council of Science Editors:

Delmar JA. A structural biology approach to the problem of antibiotic resistance in bacteria. [Thesis]. Iowa State University; 2017. Available from: https://lib.dr.iastate.edu/etd/15291

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


University of the Western Cape

12. Witbooi, Christopher Jerome. In vitro investigation of putative interactions between the RING finger domain of Retinoblastoma Binding Protein 6 (RBBP6) and various substrates .

Degree: 2015, University of the Western Cape

 Retinoblastoma Binding Protein 6 (RBBP6) is a RING finger-containing protein which plays a critical role in the 3'-end processing of mRNA transcripts. It is a… (more)

Subjects/Keywords: Retinoblastoma Binding Protein 6 (RBBP6); Cancer; Ubiquitination; ; Polymerase chain reaction; Multidrug Resistance-Associated Proteins

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APA (6th Edition):

Witbooi, C. J. (2015). In vitro investigation of putative interactions between the RING finger domain of Retinoblastoma Binding Protein 6 (RBBP6) and various substrates . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/5347

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):

Witbooi, Christopher Jerome. “In vitro investigation of putative interactions between the RING finger domain of Retinoblastoma Binding Protein 6 (RBBP6) and various substrates .” 2015. Thesis, University of the Western Cape. Accessed April 15, 2021. http://hdl.handle.net/11394/5347.

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

MLA Handbook (7th Edition):

Witbooi, Christopher Jerome. “In vitro investigation of putative interactions between the RING finger domain of Retinoblastoma Binding Protein 6 (RBBP6) and various substrates .” 2015. Web. 15 Apr 2021.

Vancouver:

Witbooi CJ. In vitro investigation of putative interactions between the RING finger domain of Retinoblastoma Binding Protein 6 (RBBP6) and various substrates . [Internet] [Thesis]. University of the Western Cape; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11394/5347.

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

Council of Science Editors:

Witbooi CJ. In vitro investigation of putative interactions between the RING finger domain of Retinoblastoma Binding Protein 6 (RBBP6) and various substrates . [Thesis]. University of the Western Cape; 2015. Available from: http://hdl.handle.net/11394/5347

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


Tampere University

13. Haukipää, Mia. Efflux-geenien ilmentyminen hiPS-soluista erilaistetuissa sarveiskalvon epiteelisoluissa .

Degree: 2014, Tampere University

 Sarveiskalvon epiteelin on opittu ilmentävän efflux-proteiineja MRP1-6 (multiresistance protein 1-6), P-gp (P-glykoproteiini) ja BCRP (breast cancer resistance protein), jotka pumppaavat substraattejaan ulos solusta. Tämän tiedon… (more)

Subjects/Keywords: sarveiskalvon epiteeli; hiPSC; HCE; efflux-kuljettajaproteiini; multidrug resistance protein; P-glykoproteiini; breast cancer related proteiini

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APA (6th Edition):

Haukipää, M. (2014). Efflux-geenien ilmentyminen hiPS-soluista erilaistetuissa sarveiskalvon epiteelisoluissa . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/96116

Chicago Manual of Style (16th Edition):

Haukipää, Mia. “Efflux-geenien ilmentyminen hiPS-soluista erilaistetuissa sarveiskalvon epiteelisoluissa .” 2014. Masters Thesis, Tampere University. Accessed April 15, 2021. https://trepo.tuni.fi/handle/10024/96116.

MLA Handbook (7th Edition):

Haukipää, Mia. “Efflux-geenien ilmentyminen hiPS-soluista erilaistetuissa sarveiskalvon epiteelisoluissa .” 2014. Web. 15 Apr 2021.

Vancouver:

Haukipää M. Efflux-geenien ilmentyminen hiPS-soluista erilaistetuissa sarveiskalvon epiteelisoluissa . [Internet] [Masters thesis]. Tampere University; 2014. [cited 2021 Apr 15]. Available from: https://trepo.tuni.fi/handle/10024/96116.

Council of Science Editors:

Haukipää M. Efflux-geenien ilmentyminen hiPS-soluista erilaistetuissa sarveiskalvon epiteelisoluissa . [Masters Thesis]. Tampere University; 2014. Available from: https://trepo.tuni.fi/handle/10024/96116


Universiteit Utrecht

14. Lagas, J.S. Pharmacological functions of multidrug transporters: studies employing combination transporter knockout mice.

Degree: 2009, Universiteit Utrecht

 ATP-binding cassette (ABC) multidrug transporters are drug efflux pumps located in the plasma membrane that utilize the energy of ATP hydrolysis to extrude a wide… (more)

Subjects/Keywords: Farmacie; ATP-binding cassette (ABC); ABC multidrug transporter; ABC transporter knockout mice; Combination transporter knockout mice; P-glycoprotein; Multidrug Resistance Protein 2; Breast Cancer Resistance Protein; Multidrug Resistance; Pharmacokinetics; Blood-brain barrier

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

APA (6th Edition):

Lagas, J. S. (2009). Pharmacological functions of multidrug transporters: studies employing combination transporter knockout mice. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/34065

Chicago Manual of Style (16th Edition):

Lagas, J S. “Pharmacological functions of multidrug transporters: studies employing combination transporter knockout mice.” 2009. Doctoral Dissertation, Universiteit Utrecht. Accessed April 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/34065.

MLA Handbook (7th Edition):

Lagas, J S. “Pharmacological functions of multidrug transporters: studies employing combination transporter knockout mice.” 2009. Web. 15 Apr 2021.

Vancouver:

Lagas JS. Pharmacological functions of multidrug transporters: studies employing combination transporter knockout mice. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2009. [cited 2021 Apr 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/34065.

Council of Science Editors:

Lagas JS. Pharmacological functions of multidrug transporters: studies employing combination transporter knockout mice. [Doctoral Dissertation]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/34065


University of Technology, Sydney

15. Lu, Jamie Fung. Microparticles mediate trait dominance in cancer.

Degree: 2015, University of Technology, Sydney

Multidrug resistance (MDR) persists to be a major hindrance to the successful treatment in clinical oncology and is the cause of over 90% of treatment… (more)

Subjects/Keywords: Multidrug resistance (MDR).; P-glycoprotein (ABCB1/P-gp).; Multidrug Resistance-associated protein 1 (ABCC1/MRP1).; Chemotherapeutic treatments.; ABC-transporter mediated MDR.; Microparticles (MPs).; MP-mediated trait dominance .

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APA (6th Edition):

Lu, J. F. (2015). Microparticles mediate trait dominance in cancer. (Thesis). University of Technology, Sydney. Retrieved from http://hdl.handle.net/10453/44200

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):

Lu, Jamie Fung. “Microparticles mediate trait dominance in cancer.” 2015. Thesis, University of Technology, Sydney. Accessed April 15, 2021. http://hdl.handle.net/10453/44200.

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

MLA Handbook (7th Edition):

Lu, Jamie Fung. “Microparticles mediate trait dominance in cancer.” 2015. Web. 15 Apr 2021.

Vancouver:

Lu JF. Microparticles mediate trait dominance in cancer. [Internet] [Thesis]. University of Technology, Sydney; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10453/44200.

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

Council of Science Editors:

Lu JF. Microparticles mediate trait dominance in cancer. [Thesis]. University of Technology, Sydney; 2015. Available from: http://hdl.handle.net/10453/44200

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

16. Verchère, Alice. Functional investigation of the efflux pump MexA–MexB-OprM of Pseudomonas aeruginosa : Etude fonctionnelle de la pompe d’efflux MexA-MexB-OprM de Pseudomonas aeruginosa.

Degree: Docteur es, Biochimie et biologie moléculaire, 2014, Université Paris Descartes – Paris V

L’efflux actif, qui permet aux bactéries d’exporter les antibiotiques vers le milieu extérieur est l’un des mécanismes majeurs de résistance aux antibiotiques. L’une des pompes… (more)

Subjects/Keywords: Resistance aux antibiotiques; Pompe d’efflux; Protéine membranaire; Protéoliposome; Test fonctionnel; Multidrug resistance; Efflux pump; Membrane protein; Proteoliposome; Functional test; 572

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APA (6th Edition):

Verchère, A. (2014). Functional investigation of the efflux pump MexA–MexB-OprM of Pseudomonas aeruginosa : Etude fonctionnelle de la pompe d’efflux MexA-MexB-OprM de Pseudomonas aeruginosa. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05P622

Chicago Manual of Style (16th Edition):

Verchère, Alice. “Functional investigation of the efflux pump MexA–MexB-OprM of Pseudomonas aeruginosa : Etude fonctionnelle de la pompe d’efflux MexA-MexB-OprM de Pseudomonas aeruginosa.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed April 15, 2021. http://www.theses.fr/2014PA05P622.

MLA Handbook (7th Edition):

Verchère, Alice. “Functional investigation of the efflux pump MexA–MexB-OprM of Pseudomonas aeruginosa : Etude fonctionnelle de la pompe d’efflux MexA-MexB-OprM de Pseudomonas aeruginosa.” 2014. Web. 15 Apr 2021.

Vancouver:

Verchère A. Functional investigation of the efflux pump MexA–MexB-OprM of Pseudomonas aeruginosa : Etude fonctionnelle de la pompe d’efflux MexA-MexB-OprM de Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2014PA05P622.

Council of Science Editors:

Verchère A. Functional investigation of the efflux pump MexA–MexB-OprM of Pseudomonas aeruginosa : Etude fonctionnelle de la pompe d’efflux MexA-MexB-OprM de Pseudomonas aeruginosa. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05P622

17. ZHANG JING. Role of multidrug resistance-associated protein 4 (MRP4/ABCC4) in the resistance and toxicity of oxazaphosphorines.

Degree: 2009, National University of Singapore

Subjects/Keywords: cyclophosphamide; ifosfamide; multidrug-associated protein 4(MRP4/ABCC4)

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APA (6th Edition):

JING, Z. (2009). Role of multidrug resistance-associated protein 4 (MRP4/ABCC4) in the resistance and toxicity of oxazaphosphorines. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/16338

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):

JING, ZHANG. “Role of multidrug resistance-associated protein 4 (MRP4/ABCC4) in the resistance and toxicity of oxazaphosphorines.” 2009. Thesis, National University of Singapore. Accessed April 15, 2021. http://scholarbank.nus.edu.sg/handle/10635/16338.

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

MLA Handbook (7th Edition):

JING, ZHANG. “Role of multidrug resistance-associated protein 4 (MRP4/ABCC4) in the resistance and toxicity of oxazaphosphorines.” 2009. Web. 15 Apr 2021.

Vancouver:

JING Z. Role of multidrug resistance-associated protein 4 (MRP4/ABCC4) in the resistance and toxicity of oxazaphosphorines. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2021 Apr 15]. Available from: http://scholarbank.nus.edu.sg/handle/10635/16338.

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

Council of Science Editors:

JING Z. Role of multidrug resistance-associated protein 4 (MRP4/ABCC4) in the resistance and toxicity of oxazaphosphorines. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/16338

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

18. Bachas, Sharrol T. Multidrug recognition and Multidrug transcription activation by the gene regulator, BmrR.

Degree: 2014, Johns Hopkins University

Multidrug resistance (MDR) is conferred by multidrug (MD) transporters and MD-responsive gene regulators. Intriguingly, regulation of MD transporters and gene regulators depend on interactions with… (more)

Subjects/Keywords: Multidrug resistance; Multidrug recogniton,Multidrug signaling; Transcriptional activation; MerR family

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APA (6th Edition):

Bachas, S. T. (2014). Multidrug recognition and Multidrug transcription activation by the gene regulator, BmrR. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37156

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):

Bachas, Sharrol T. “Multidrug recognition and Multidrug transcription activation by the gene regulator, BmrR.” 2014. Thesis, Johns Hopkins University. Accessed April 15, 2021. http://jhir.library.jhu.edu/handle/1774.2/37156.

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

MLA Handbook (7th Edition):

Bachas, Sharrol T. “Multidrug recognition and Multidrug transcription activation by the gene regulator, BmrR.” 2014. Web. 15 Apr 2021.

Vancouver:

Bachas ST. Multidrug recognition and Multidrug transcription activation by the gene regulator, BmrR. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2021 Apr 15]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37156.

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

Council of Science Editors:

Bachas ST. Multidrug recognition and Multidrug transcription activation by the gene regulator, BmrR. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/37156

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


University of Utah

19. Kim, Dongin. pH-Sensitive Micelle for Multidrug Resistant Tumors.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2010, University of Utah

 The goal of this hypothesis-driven application is to develop a polymeric micelle that targets multidrug resistant (MDR) tumors via pH sensitivity. The micelles target tumors… (more)

Subjects/Keywords: Micelles; Cancer; Multidrug Resistance

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

APA (6th Edition):

Kim, D. (2010). pH-Sensitive Micelle for Multidrug Resistant Tumors. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2149/rec/881

Chicago Manual of Style (16th Edition):

Kim, Dongin. “pH-Sensitive Micelle for Multidrug Resistant Tumors.” 2010. Doctoral Dissertation, University of Utah. Accessed April 15, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2149/rec/881.

MLA Handbook (7th Edition):

Kim, Dongin. “pH-Sensitive Micelle for Multidrug Resistant Tumors.” 2010. Web. 15 Apr 2021.

Vancouver:

Kim D. pH-Sensitive Micelle for Multidrug Resistant Tumors. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 Apr 15]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2149/rec/881.

Council of Science Editors:

Kim D. pH-Sensitive Micelle for Multidrug Resistant Tumors. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/2149/rec/881


Queens University

20. Myette, Robert Leonard. Chalcogenopyrylium Dyes as Modulators of Multidrug Resistance Protein (MRP) 1, MRP2 and MRP4 Transport Activities .

Degree: Pathology and Molecular Medicine, 2011, Queens University

 MRPs mediate the ATP-dependent efflux of a structurally diverse array of compounds. Certain MRPs, including MRP1, MRP2 and MRP4, are involved in multidrug resistance in… (more)

Subjects/Keywords: Multidrug Resistance Proteins ; Chalcogenopyrylium Dyes

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APA (6th Edition):

Myette, R. L. (2011). Chalcogenopyrylium Dyes as Modulators of Multidrug Resistance Protein (MRP) 1, MRP2 and MRP4 Transport Activities . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6891

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):

Myette, Robert Leonard. “Chalcogenopyrylium Dyes as Modulators of Multidrug Resistance Protein (MRP) 1, MRP2 and MRP4 Transport Activities .” 2011. Thesis, Queens University. Accessed April 15, 2021. http://hdl.handle.net/1974/6891.

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

MLA Handbook (7th Edition):

Myette, Robert Leonard. “Chalcogenopyrylium Dyes as Modulators of Multidrug Resistance Protein (MRP) 1, MRP2 and MRP4 Transport Activities .” 2011. Web. 15 Apr 2021.

Vancouver:

Myette RL. Chalcogenopyrylium Dyes as Modulators of Multidrug Resistance Protein (MRP) 1, MRP2 and MRP4 Transport Activities . [Internet] [Thesis]. Queens University; 2011. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1974/6891.

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

Council of Science Editors:

Myette RL. Chalcogenopyrylium Dyes as Modulators of Multidrug Resistance Protein (MRP) 1, MRP2 and MRP4 Transport Activities . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6891

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


University of Oklahoma

21. Ntreh, Abigail. Mechanism and Interactions of Inner and Outer Membrane Components of RND Efflux Pumps.

Degree: PhD, 2016, University of Oklahoma

 Since the discovery of antibiotics, an ongoing race commenced between society’s ability to develop drugs and resistant bacteria. The combat has led to many drug… (more)

Subjects/Keywords: mechanism; multidrug resistance; efflux pumps

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APA (6th Edition):

Ntreh, A. (2016). Mechanism and Interactions of Inner and Outer Membrane Components of RND Efflux Pumps. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/44931

Chicago Manual of Style (16th Edition):

Ntreh, Abigail. “Mechanism and Interactions of Inner and Outer Membrane Components of RND Efflux Pumps.” 2016. Doctoral Dissertation, University of Oklahoma. Accessed April 15, 2021. http://hdl.handle.net/11244/44931.

MLA Handbook (7th Edition):

Ntreh, Abigail. “Mechanism and Interactions of Inner and Outer Membrane Components of RND Efflux Pumps.” 2016. Web. 15 Apr 2021.

Vancouver:

Ntreh A. Mechanism and Interactions of Inner and Outer Membrane Components of RND Efflux Pumps. [Internet] [Doctoral dissertation]. University of Oklahoma; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11244/44931.

Council of Science Editors:

Ntreh A. Mechanism and Interactions of Inner and Outer Membrane Components of RND Efflux Pumps. [Doctoral Dissertation]. University of Oklahoma; 2016. Available from: http://hdl.handle.net/11244/44931


University of Oxford

22. Ma, Jerome H. Y. Atomistic studies of the dynamics of P-glycoprotein and its ligands.

Degree: PhD, 2013, University of Oxford

 A signifficant obstacle facing the healthcare industry is the phenomenon of multidrug resistance (MDR) in which a cell acquires simultaneous resistance to many unrelated drugs… (more)

Subjects/Keywords: 572; Biochemistry; Computational chemistry; Molecular dynamics; Nuclear magnetic resonance; Structural Biology; P-glycoprotein; Membrane protein; Lipid bilayer; Multidrug resistance

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APA (6th Edition):

Ma, J. H. Y. (2013). Atomistic studies of the dynamics of P-glycoprotein and its ligands. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:e2e2bbe0-d4ae-4351-b339-c8e02ef3d3d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658390

Chicago Manual of Style (16th Edition):

Ma, Jerome H Y. “Atomistic studies of the dynamics of P-glycoprotein and its ligands.” 2013. Doctoral Dissertation, University of Oxford. Accessed April 15, 2021. http://ora.ox.ac.uk/objects/uuid:e2e2bbe0-d4ae-4351-b339-c8e02ef3d3d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658390.

MLA Handbook (7th Edition):

Ma, Jerome H Y. “Atomistic studies of the dynamics of P-glycoprotein and its ligands.” 2013. Web. 15 Apr 2021.

Vancouver:

Ma JHY. Atomistic studies of the dynamics of P-glycoprotein and its ligands. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2021 Apr 15]. Available from: http://ora.ox.ac.uk/objects/uuid:e2e2bbe0-d4ae-4351-b339-c8e02ef3d3d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658390.

Council of Science Editors:

Ma JHY. Atomistic studies of the dynamics of P-glycoprotein and its ligands. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:e2e2bbe0-d4ae-4351-b339-c8e02ef3d3d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.658390


Clemson University

23. Green, Benjamin. FOSINOPRIL, A POTENTIAL SUBSTRATE FOR MRP2, COMPETES WITH SEVERAL HIGH USE PHARMACEUTICALS FOR ELIMINATION.

Degree: MS, Biological Sciences, 2010, Clemson University

 The multidrug-resistance associated protein 2 (MRP2) is a membrane-bound transporter responsible for the efflux of a variety of drugs and endogenous compounds. MDCK cells transfected… (more)

Subjects/Keywords: : Multidrug resistance-associated protein 2; fosinopril; methotrexate; Molecular Biology

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APA (6th Edition):

Green, B. (2010). FOSINOPRIL, A POTENTIAL SUBSTRATE FOR MRP2, COMPETES WITH SEVERAL HIGH USE PHARMACEUTICALS FOR ELIMINATION. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/893

Chicago Manual of Style (16th Edition):

Green, Benjamin. “FOSINOPRIL, A POTENTIAL SUBSTRATE FOR MRP2, COMPETES WITH SEVERAL HIGH USE PHARMACEUTICALS FOR ELIMINATION.” 2010. Masters Thesis, Clemson University. Accessed April 15, 2021. https://tigerprints.clemson.edu/all_theses/893.

MLA Handbook (7th Edition):

Green, Benjamin. “FOSINOPRIL, A POTENTIAL SUBSTRATE FOR MRP2, COMPETES WITH SEVERAL HIGH USE PHARMACEUTICALS FOR ELIMINATION.” 2010. Web. 15 Apr 2021.

Vancouver:

Green B. FOSINOPRIL, A POTENTIAL SUBSTRATE FOR MRP2, COMPETES WITH SEVERAL HIGH USE PHARMACEUTICALS FOR ELIMINATION. [Internet] [Masters thesis]. Clemson University; 2010. [cited 2021 Apr 15]. Available from: https://tigerprints.clemson.edu/all_theses/893.

Council of Science Editors:

Green B. FOSINOPRIL, A POTENTIAL SUBSTRATE FOR MRP2, COMPETES WITH SEVERAL HIGH USE PHARMACEUTICALS FOR ELIMINATION. [Masters Thesis]. Clemson University; 2010. Available from: https://tigerprints.clemson.edu/all_theses/893


University of Sydney

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

Degree: 2015, University of Sydney

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Seebacher, Nicole Aveline. “Overcoming the Dual Mechanism of Stress-Induced, Pgp-Mediated Drug Resistance using Novel Thiosemicarbazones .” 2015. Thesis, University of Sydney. Accessed April 15, 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. 15 Apr 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 Apr 15]. 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

25. Schäfer, Andreas. Synthese des Cyclohepta[e]hydrindan-Kerns des marinen Homoverrucosan-Diterpenoids Gagunin E und Evaluation von Homoverrucosanoid-abgeleiteten Estern als MDR-Modulatoren.

Degree: 2018, Technische Universität Dortmund

 The present thesis describes the synthesis of the A−B-cis,B−C-trans annulated cyclohepta[e]hydrindane core of a gagunin E analogue featuring a fully elaborated B−C ring segment. The… (more)

Subjects/Keywords: Homoverrucosan-Diterpenoid; Gagunin E; Ringschlussmetathese (RCM); (4+2)-Cycloaddition; Cyclopropanierung und Ringöffnung; Multidrug Resistance (MDR)-Modulatoren; Homoverrucosane diterpenoid; Gagunin E; Ring-closing metathesis (RCM); (4+2)-cycloaddition; Cyclopropanation−ring opening; Multidrug esistance (MDR) modulators; 540; Metathese; Cycloaddition

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APA (6th Edition):

Schäfer, A. (2018). Synthese des Cyclohepta[e]hydrindan-Kerns des marinen Homoverrucosan-Diterpenoids Gagunin E und Evaluation von Homoverrucosanoid-abgeleiteten Estern als MDR-Modulatoren. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-18900

Chicago Manual of Style (16th Edition):

Schäfer, Andreas. “Synthese des Cyclohepta[e]hydrindan-Kerns des marinen Homoverrucosan-Diterpenoids Gagunin E und Evaluation von Homoverrucosanoid-abgeleiteten Estern als MDR-Modulatoren.” 2018. Doctoral Dissertation, Technische Universität Dortmund. Accessed April 15, 2021. http://dx.doi.org/10.17877/DE290R-18900.

MLA Handbook (7th Edition):

Schäfer, Andreas. “Synthese des Cyclohepta[e]hydrindan-Kerns des marinen Homoverrucosan-Diterpenoids Gagunin E und Evaluation von Homoverrucosanoid-abgeleiteten Estern als MDR-Modulatoren.” 2018. Web. 15 Apr 2021.

Vancouver:

Schäfer A. Synthese des Cyclohepta[e]hydrindan-Kerns des marinen Homoverrucosan-Diterpenoids Gagunin E und Evaluation von Homoverrucosanoid-abgeleiteten Estern als MDR-Modulatoren. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2018. [cited 2021 Apr 15]. Available from: http://dx.doi.org/10.17877/DE290R-18900.

Council of Science Editors:

Schäfer A. Synthese des Cyclohepta[e]hydrindan-Kerns des marinen Homoverrucosan-Diterpenoids Gagunin E und Evaluation von Homoverrucosanoid-abgeleiteten Estern als MDR-Modulatoren. [Doctoral Dissertation]. Technische Universität Dortmund; 2018. Available from: http://dx.doi.org/10.17877/DE290R-18900

26. Papavasileiou, Vasileios. Διερεύνηση της σχέσης μεταξύ retinol binding protein 4 και της αντίστασης στην ινσουλίνη στον αιμοκαθαιρόμενο πληθυσμό.

Degree: 2017, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας

Introduction: The Retinol Binding Protein-4 (RBP-4) is a unique, special protein-carrier of retinol (vitamin A) in blood and until recently, the only known function was… (more)

Subjects/Keywords: Αντίσταση στην ινσουλίνη; Δεσμεύουσα τη ρετινόλη πρωτεΐνη 4; Αιμοκάθαρση; Insulin resistance; Retinol binding protein 4; Haemodialysis

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APA (6th Edition):

Papavasileiou, V. (2017). Διερεύνηση της σχέσης μεταξύ retinol binding protein 4 και της αντίστασης στην ινσουλίνη στον αιμοκαθαιρόμενο πληθυσμό. (Thesis). University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Retrieved from http://hdl.handle.net/10442/hedi/42412

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):

Papavasileiou, Vasileios. “Διερεύνηση της σχέσης μεταξύ retinol binding protein 4 και της αντίστασης στην ινσουλίνη στον αιμοκαθαιρόμενο πληθυσμό.” 2017. Thesis, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Accessed April 15, 2021. http://hdl.handle.net/10442/hedi/42412.

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

MLA Handbook (7th Edition):

Papavasileiou, Vasileios. “Διερεύνηση της σχέσης μεταξύ retinol binding protein 4 και της αντίστασης στην ινσουλίνη στον αιμοκαθαιρόμενο πληθυσμό.” 2017. Web. 15 Apr 2021.

Vancouver:

Papavasileiou V. Διερεύνηση της σχέσης μεταξύ retinol binding protein 4 και της αντίστασης στην ινσουλίνη στον αιμοκαθαιρόμενο πληθυσμό. [Internet] [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10442/hedi/42412.

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

Council of Science Editors:

Papavasileiou V. Διερεύνηση της σχέσης μεταξύ retinol binding protein 4 και της αντίστασης στην ινσουλίνη στον αιμοκαθαιρόμενο πληθυσμό. [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2017. Available from: http://hdl.handle.net/10442/hedi/42412

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


University of California – Merced

27. Mahaffey, Christopher M. Multidrug resistant protein-three gene regulation.

Degree: Quantitative and Systems Biology, 2010, University of California – Merced

 This dissertation is presented in two sections. Section one recounts my investigations of modulating the multidrug-resistant protein-three (MRP3) levels, by either activating or silencing the… (more)

Subjects/Keywords: Biology.; Multidrug resistance.; Gene regulation.; MRP3.

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

APA (6th Edition):

Mahaffey, C. M. (2010). Multidrug resistant protein-three gene regulation. (Thesis). University of California – Merced. Retrieved from http://www.escholarship.org/uc/item/14h425vs

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):

Mahaffey, Christopher M. “Multidrug resistant protein-three gene regulation.” 2010. Thesis, University of California – Merced. Accessed April 15, 2021. http://www.escholarship.org/uc/item/14h425vs.

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

MLA Handbook (7th Edition):

Mahaffey, Christopher M. “Multidrug resistant protein-three gene regulation.” 2010. Web. 15 Apr 2021.

Vancouver:

Mahaffey CM. Multidrug resistant protein-three gene regulation. [Internet] [Thesis]. University of California – Merced; 2010. [cited 2021 Apr 15]. Available from: http://www.escholarship.org/uc/item/14h425vs.

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

Council of Science Editors:

Mahaffey CM. Multidrug resistant protein-three gene regulation. [Thesis]. University of California – Merced; 2010. Available from: http://www.escholarship.org/uc/item/14h425vs

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


California State University – Northridge

28. Yazdani, Arash. Characterization of a TetR/AcrR family transcriptional repressor gene NpR3597 in Nostoc punctiforme.

Degree: MS, Biology, 2012, California State University – Northridge

 Nostoc punctiforme is a filamentous cyanobacterium capable of differentiating its vegetative cells into spore-like akinetes that can withstand desiccation and cold. The NpR3597 gene was… (more)

Subjects/Keywords: Multidrug resistance; Dissertations, Academic  – CSUN  – Biology.

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APA (6th Edition):

Yazdani, A. (2012). Characterization of a TetR/AcrR family transcriptional repressor gene NpR3597 in Nostoc punctiforme. (Masters Thesis). California State University – Northridge. Retrieved from http://hdl.handle.net/10211.2/1198

Chicago Manual of Style (16th Edition):

Yazdani, Arash. “Characterization of a TetR/AcrR family transcriptional repressor gene NpR3597 in Nostoc punctiforme.” 2012. Masters Thesis, California State University – Northridge. Accessed April 15, 2021. http://hdl.handle.net/10211.2/1198.

MLA Handbook (7th Edition):

Yazdani, Arash. “Characterization of a TetR/AcrR family transcriptional repressor gene NpR3597 in Nostoc punctiforme.” 2012. Web. 15 Apr 2021.

Vancouver:

Yazdani A. Characterization of a TetR/AcrR family transcriptional repressor gene NpR3597 in Nostoc punctiforme. [Internet] [Masters thesis]. California State University – Northridge; 2012. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10211.2/1198.

Council of Science Editors:

Yazdani A. Characterization of a TetR/AcrR family transcriptional repressor gene NpR3597 in Nostoc punctiforme. [Masters Thesis]. California State University – Northridge; 2012. Available from: http://hdl.handle.net/10211.2/1198


Queens University

29. Csandl, Mark. The Effect of Leukotriene Modifiers (LTMs) on Organic Anion Transport by Multidrug Resistance Proteins (MRPs) .

Degree: Pharmacology and Toxicology, 2015, Queens University

 The multidrug resistance proteins (MRPs) are plasma membrane efflux transporters that transport a diverse array of compounds. MRP1, MRP2, MRP3 and MRP4 are considered the… (more)

Subjects/Keywords: Multidrug resistance proteins ; Leukotriene receptor antagonists

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

APA (6th Edition):

Csandl, M. (2015). The Effect of Leukotriene Modifiers (LTMs) on Organic Anion Transport by Multidrug Resistance Proteins (MRPs) . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13502

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):

Csandl, Mark. “The Effect of Leukotriene Modifiers (LTMs) on Organic Anion Transport by Multidrug Resistance Proteins (MRPs) .” 2015. Thesis, Queens University. Accessed April 15, 2021. http://hdl.handle.net/1974/13502.

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

MLA Handbook (7th Edition):

Csandl, Mark. “The Effect of Leukotriene Modifiers (LTMs) on Organic Anion Transport by Multidrug Resistance Proteins (MRPs) .” 2015. Web. 15 Apr 2021.

Vancouver:

Csandl M. The Effect of Leukotriene Modifiers (LTMs) on Organic Anion Transport by Multidrug Resistance Proteins (MRPs) . [Internet] [Thesis]. Queens University; 2015. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1974/13502.

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

Council of Science Editors:

Csandl M. The Effect of Leukotriene Modifiers (LTMs) on Organic Anion Transport by Multidrug Resistance Proteins (MRPs) . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13502

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


University of Manitoba

30. Singh, Cathleen. Phenotypic and genotypic characterization of high-level macrolide and lincosamide resistance in Corynebacterium species in Canada and the distribution of the ermX resistance determinant among Corynebacterium species.

Degree: Medical Microbiology, 2010, University of Manitoba

 Specific bacterial commensals demonstrating multidrug resistance (MDR) are opportunistic pathogens for immunocompromised patients, including Corynebacterium species (spp.). Severe infections due to MDR corynebacteria are being… (more)

Subjects/Keywords: Corynebacterium; macrolide; resistance; ermX; multidrug; resistant

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

APA (6th Edition):

Singh, C. (2010). Phenotypic and genotypic characterization of high-level macrolide and lincosamide resistance in Corynebacterium species in Canada and the distribution of the ermX resistance determinant among Corynebacterium species. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/3974

Chicago Manual of Style (16th Edition):

Singh, Cathleen. “Phenotypic and genotypic characterization of high-level macrolide and lincosamide resistance in Corynebacterium species in Canada and the distribution of the ermX resistance determinant among Corynebacterium species.” 2010. Masters Thesis, University of Manitoba. Accessed April 15, 2021. http://hdl.handle.net/1993/3974.

MLA Handbook (7th Edition):

Singh, Cathleen. “Phenotypic and genotypic characterization of high-level macrolide and lincosamide resistance in Corynebacterium species in Canada and the distribution of the ermX resistance determinant among Corynebacterium species.” 2010. Web. 15 Apr 2021.

Vancouver:

Singh C. Phenotypic and genotypic characterization of high-level macrolide and lincosamide resistance in Corynebacterium species in Canada and the distribution of the ermX resistance determinant among Corynebacterium species. [Internet] [Masters thesis]. University of Manitoba; 2010. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1993/3974.

Council of Science Editors:

Singh C. Phenotypic and genotypic characterization of high-level macrolide and lincosamide resistance in Corynebacterium species in Canada and the distribution of the ermX resistance determinant among Corynebacterium species. [Masters Thesis]. University of Manitoba; 2010. Available from: http://hdl.handle.net/1993/3974

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