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You searched for subject:(multidrug associated protein 4 MRP4 ABCC4 ). Showing records 1 – 30 of 29013 total matches.

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1. 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 10, 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. 10 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 10]. 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

2. 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 10, 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. 10 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 10]. 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


Texas State University – San Marcos

3. 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 10, 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. 10 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 10]. 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


University of New South Wales

4. Huynh, Tony. The Identification and Characterisation of Small Molecule Inhibitors of MRP4 for the Potential Treatment of Childhood Neuroblastoma.

Degree: Women's & Children's Health, 2016, University of New South Wales

Multidrug resistance is one of the major causes of treatment failure in cancer therapy. While multidrug transporter proteins are known for their contributions to chemotherapy… (more)

Subjects/Keywords: ATP-binding cassette transporter protein; neuroblastoma; MRP4/ABCC4

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APA (6th Edition):

Huynh, T. (2016). The Identification and Characterisation of Small Molecule Inhibitors of MRP4 for the Potential Treatment of Childhood Neuroblastoma. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/57118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42548/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Huynh, Tony. “The Identification and Characterisation of Small Molecule Inhibitors of MRP4 for the Potential Treatment of Childhood Neuroblastoma.” 2016. Doctoral Dissertation, University of New South Wales. Accessed April 10, 2021. http://handle.unsw.edu.au/1959.4/57118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42548/SOURCE02?view=true.

MLA Handbook (7th Edition):

Huynh, Tony. “The Identification and Characterisation of Small Molecule Inhibitors of MRP4 for the Potential Treatment of Childhood Neuroblastoma.” 2016. Web. 10 Apr 2021.

Vancouver:

Huynh T. The Identification and Characterisation of Small Molecule Inhibitors of MRP4 for the Potential Treatment of Childhood Neuroblastoma. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2021 Apr 10]. Available from: http://handle.unsw.edu.au/1959.4/57118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42548/SOURCE02?view=true.

Council of Science Editors:

Huynh T. The Identification and Characterisation of Small Molecule Inhibitors of MRP4 for the Potential Treatment of Childhood Neuroblastoma. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/57118 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:42548/SOURCE02?view=true


Queens University

5. 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 (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 10, 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. 10 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 10]. 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


University of the Western Cape

6. 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 10, 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. 10 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 10]. 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


Clemson University

7. 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 10, 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. 10 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 10]. 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 Technology, Sydney

8. 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 10, 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. 10 Apr 2021.

Vancouver:

Lu JF. Microparticles mediate trait dominance in cancer. [Internet] [Thesis]. University of Technology, Sydney; 2015. [cited 2021 Apr 10]. 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

9. GONG, CHAO. Analysis of the Human Microtubule Interactome Using Multidimensional Chromatography and Tandem Mass Spectrometry.

Degree: PhD, Chemistry, 2013, Brown University

 Recent developments in mass spectrometer technology has increased the sensitivity and speed to an unprecedented level, along with the continuing improvements of high performance liquid… (more)

Subjects/Keywords: microtubule associated protein

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APA (6th Edition):

GONG, C. (2013). Analysis of the Human Microtubule Interactome Using Multidimensional Chromatography and Tandem Mass Spectrometry. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:320463/

Chicago Manual of Style (16th Edition):

GONG, CHAO. “Analysis of the Human Microtubule Interactome Using Multidimensional Chromatography and Tandem Mass Spectrometry.” 2013. Doctoral Dissertation, Brown University. Accessed April 10, 2021. https://repository.library.brown.edu/studio/item/bdr:320463/.

MLA Handbook (7th Edition):

GONG, CHAO. “Analysis of the Human Microtubule Interactome Using Multidimensional Chromatography and Tandem Mass Spectrometry.” 2013. Web. 10 Apr 2021.

Vancouver:

GONG C. Analysis of the Human Microtubule Interactome Using Multidimensional Chromatography and Tandem Mass Spectrometry. [Internet] [Doctoral dissertation]. Brown University; 2013. [cited 2021 Apr 10]. Available from: https://repository.library.brown.edu/studio/item/bdr:320463/.

Council of Science Editors:

GONG C. Analysis of the Human Microtubule Interactome Using Multidimensional Chromatography and Tandem Mass Spectrometry. [Doctoral Dissertation]. Brown University; 2013. Available from: https://repository.library.brown.edu/studio/item/bdr:320463/


UCLA

10. Chen, Eric. Neurexin Family Member Contactin-Associated Protein Like-4 (CNTNAP4) is a specific cell membrane receptor of Neural EGFL Like 1 (NELL1).

Degree: Oral Biology, 2018, UCLA

 Secretory protein neural EGFL like 1 (Nell-1) has been shown to exert potent osteogenic effects in multiple small and large animal models. Here, we identified… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Cellular biology; Contactin-associated protein-like 4 (Cntnap4); Neural EGFL like 1 (Nell-1); Osteogenesis; Receptor

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APA (6th Edition):

Chen, E. (2018). Neurexin Family Member Contactin-Associated Protein Like-4 (CNTNAP4) is a specific cell membrane receptor of Neural EGFL Like 1 (NELL1). (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/67b4g7v5

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):

Chen, Eric. “Neurexin Family Member Contactin-Associated Protein Like-4 (CNTNAP4) is a specific cell membrane receptor of Neural EGFL Like 1 (NELL1).” 2018. Thesis, UCLA. Accessed April 10, 2021. http://www.escholarship.org/uc/item/67b4g7v5.

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

MLA Handbook (7th Edition):

Chen, Eric. “Neurexin Family Member Contactin-Associated Protein Like-4 (CNTNAP4) is a specific cell membrane receptor of Neural EGFL Like 1 (NELL1).” 2018. Web. 10 Apr 2021.

Vancouver:

Chen E. Neurexin Family Member Contactin-Associated Protein Like-4 (CNTNAP4) is a specific cell membrane receptor of Neural EGFL Like 1 (NELL1). [Internet] [Thesis]. UCLA; 2018. [cited 2021 Apr 10]. Available from: http://www.escholarship.org/uc/item/67b4g7v5.

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

Council of Science Editors:

Chen E. Neurexin Family Member Contactin-Associated Protein Like-4 (CNTNAP4) is a specific cell membrane receptor of Neural EGFL Like 1 (NELL1). [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/67b4g7v5

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


Queens University

11. 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 10, 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. 10 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 10]. 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


NSYSU

12. Hsieh, Li-Chen. Light-triggered Oncolytic Virotherapy Overcome Multidrug Resistance Cancer.

Degree: Master, Institute of Medical Science and Technology, 2016, NSYSU

 Recently, multidrug-resistant (MDR) is one of the major challenges in cancer therapy when the patients have been treated with the chemotherapy. Among potential factors associated(more)

Subjects/Keywords: Photodynamic therapy; Adeno-associated virus; Multidrug Resistance; Iron oxide nanoparticles; KillerRed

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APA (6th Edition):

Hsieh, L. (2016). Light-triggered Oncolytic Virotherapy Overcome Multidrug Resistance Cancer. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0729116-142939

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):

Hsieh, Li-Chen. “Light-triggered Oncolytic Virotherapy Overcome Multidrug Resistance Cancer.” 2016. Thesis, NSYSU. Accessed April 10, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0729116-142939.

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

MLA Handbook (7th Edition):

Hsieh, Li-Chen. “Light-triggered Oncolytic Virotherapy Overcome Multidrug Resistance Cancer.” 2016. Web. 10 Apr 2021.

Vancouver:

Hsieh L. Light-triggered Oncolytic Virotherapy Overcome Multidrug Resistance Cancer. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Apr 10]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0729116-142939.

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

Council of Science Editors:

Hsieh L. Light-triggered Oncolytic Virotherapy Overcome Multidrug Resistance Cancer. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0729116-142939

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


University of Kansas

13. Mitra, Pallabi. ROLES OF SULFOTRANSFERASE ENZYMES IN TRANS-PLACENTAL DISPOSITION.

Degree: PhD, Pharmaceutical Chemistry, 2009, University of Kansas

 The trophoblast cell layer constitutes the rate-determining barrier for trans-placental transfer. Several isoforms of the sulfotransferase enzymes are functional in placenta but there is only… (more)

Subjects/Keywords: Pharmaceutical chemistry; Bisphenol a; Breast cancer resistance protein (bcrp); Multidrug resistance-associated protein (mrp); Placenta; Sulfotransferase enzymes; Trophoblast

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APA (6th Edition):

Mitra, P. (2009). ROLES OF SULFOTRANSFERASE ENZYMES IN TRANS-PLACENTAL DISPOSITION. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6185

Chicago Manual of Style (16th Edition):

Mitra, Pallabi. “ROLES OF SULFOTRANSFERASE ENZYMES IN TRANS-PLACENTAL DISPOSITION.” 2009. Doctoral Dissertation, University of Kansas. Accessed April 10, 2021. http://hdl.handle.net/1808/6185.

MLA Handbook (7th Edition):

Mitra, Pallabi. “ROLES OF SULFOTRANSFERASE ENZYMES IN TRANS-PLACENTAL DISPOSITION.” 2009. Web. 10 Apr 2021.

Vancouver:

Mitra P. ROLES OF SULFOTRANSFERASE ENZYMES IN TRANS-PLACENTAL DISPOSITION. [Internet] [Doctoral dissertation]. University of Kansas; 2009. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1808/6185.

Council of Science Editors:

Mitra P. ROLES OF SULFOTRANSFERASE ENZYMES IN TRANS-PLACENTAL DISPOSITION. [Doctoral Dissertation]. University of Kansas; 2009. Available from: http://hdl.handle.net/1808/6185

14. Massot, Bérangère. Etudes de populations lymphocytaires T naturelles productrices d'IL-17 : iNKT17 et Th17 : Studies of populations natural lymphocytaires T producers of IL-17 : iNKT17 and Th17.

Degree: Docteur es, Immunologie, 2012, Université Paris Descartes – Paris V

 Le thymus est un organe permettant le développement des lymphocytes T, partie intégrante du système immunitaire. Ces cellules sont communément associées au système immunitaire adaptatif,… (more)

Subjects/Keywords: Cellules T; SLAM‐associated protein

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APA (6th Edition):

Massot, B. (2012). Etudes de populations lymphocytaires T naturelles productrices d'IL-17 : iNKT17 et Th17 : Studies of populations natural lymphocytaires T producers of IL-17 : iNKT17 and Th17. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2012PA05T036

Chicago Manual of Style (16th Edition):

Massot, Bérangère. “Etudes de populations lymphocytaires T naturelles productrices d'IL-17 : iNKT17 et Th17 : Studies of populations natural lymphocytaires T producers of IL-17 : iNKT17 and Th17.” 2012. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed April 10, 2021. http://www.theses.fr/2012PA05T036.

MLA Handbook (7th Edition):

Massot, Bérangère. “Etudes de populations lymphocytaires T naturelles productrices d'IL-17 : iNKT17 et Th17 : Studies of populations natural lymphocytaires T producers of IL-17 : iNKT17 and Th17.” 2012. Web. 10 Apr 2021.

Vancouver:

Massot B. Etudes de populations lymphocytaires T naturelles productrices d'IL-17 : iNKT17 et Th17 : Studies of populations natural lymphocytaires T producers of IL-17 : iNKT17 and Th17. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2012. [cited 2021 Apr 10]. Available from: http://www.theses.fr/2012PA05T036.

Council of Science Editors:

Massot B. Etudes de populations lymphocytaires T naturelles productrices d'IL-17 : iNKT17 et Th17 : Studies of populations natural lymphocytaires T producers of IL-17 : iNKT17 and Th17. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2012. Available from: http://www.theses.fr/2012PA05T036


University of Toronto

15. Tan, Kah Poh. Nuclear Factor (Erythroid 2-like) Factor 2 (Nrf2) as Cellular Protector in Bile Acid and Retinoid Toxicities.

Degree: 2008, University of Toronto

Exposure to toxic bile acids (BA) and retinoic acids (RA) is implicated in toxicities related to excessive oxidative stress. This thesis examined roles and mechanisms… (more)

Subjects/Keywords: oxidative stress; glutathione; bile acid; Nrf2; retinoic acid; cholestasis; ATP-binding cassette transporters; mitogen activated protein kinase; multidrug resistance associated proteins; adaptive response; antioxidants; thioredoxin reductase; 4-hydroxynonenal; lipid peroxidation; glutathione S-transferase; liver toxicity; antioxidant response element; cell defense; 0383

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APA (6th Edition):

Tan, K. P. (2008). Nuclear Factor (Erythroid 2-like) Factor 2 (Nrf2) as Cellular Protector in Bile Acid and Retinoid Toxicities. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/17287

Chicago Manual of Style (16th Edition):

Tan, Kah Poh. “Nuclear Factor (Erythroid 2-like) Factor 2 (Nrf2) as Cellular Protector in Bile Acid and Retinoid Toxicities.” 2008. Doctoral Dissertation, University of Toronto. Accessed April 10, 2021. http://hdl.handle.net/1807/17287.

MLA Handbook (7th Edition):

Tan, Kah Poh. “Nuclear Factor (Erythroid 2-like) Factor 2 (Nrf2) as Cellular Protector in Bile Acid and Retinoid Toxicities.” 2008. Web. 10 Apr 2021.

Vancouver:

Tan KP. Nuclear Factor (Erythroid 2-like) Factor 2 (Nrf2) as Cellular Protector in Bile Acid and Retinoid Toxicities. [Internet] [Doctoral dissertation]. University of Toronto; 2008. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1807/17287.

Council of Science Editors:

Tan KP. Nuclear Factor (Erythroid 2-like) Factor 2 (Nrf2) as Cellular Protector in Bile Acid and Retinoid Toxicities. [Doctoral Dissertation]. University of Toronto; 2008. Available from: http://hdl.handle.net/1807/17287

16. TIAN QUAN. Interactions of human multidrug resistance protein 4 with camptothecins.

Degree: 2009, National University of Singapore

Subjects/Keywords: multidrug resistance; ATP-binding cassette; MRP4; camptothecin; drug transporter; glutathione

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APA (6th Edition):

QUAN, T. (2009). Interactions of human multidrug resistance protein 4 with camptothecins. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15894

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):

QUAN, TIAN. “Interactions of human multidrug resistance protein 4 with camptothecins.” 2009. Thesis, National University of Singapore. Accessed April 10, 2021. http://scholarbank.nus.edu.sg/handle/10635/15894.

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

MLA Handbook (7th Edition):

QUAN, TIAN. “Interactions of human multidrug resistance protein 4 with camptothecins.” 2009. Web. 10 Apr 2021.

Vancouver:

QUAN T. Interactions of human multidrug resistance protein 4 with camptothecins. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2021 Apr 10]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15894.

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

Council of Science Editors:

QUAN T. Interactions of human multidrug resistance protein 4 with camptothecins. [Thesis]. National University of Singapore; 2009. Available from: http://scholarbank.nus.edu.sg/handle/10635/15894

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

17. 渡辺, 喬之. Modulatiion of arsenic toxicity via MRPs in cells : 多剤耐性タンパクMRPsを介した細胞のヒ素毒性調節機構.

Degree: 博士(医薬学), 2013, Chiba University / 千葉大学

研究科: 千葉大学大学院医学薬学府

学位:千大院医薬博甲第医薬58号

Advisors/Committee Members: 千葉大学大学院医学薬学府.

Subjects/Keywords: arsenic; toxicity; metabolism; multidrug-resistance associated protein; ヒ素; 毒性; 代謝; 多剤耐性タンパク

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APA (6th Edition):

渡辺, . (2013). Modulatiion of arsenic toxicity via MRPs in cells : 多剤耐性タンパクMRPsを介した細胞のヒ素毒性調節機構. (Thesis). Chiba University / 千葉大学. Retrieved from http://opac.ll.chiba-u.jp/da/curator/900118747/

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):

渡辺, 喬之. “Modulatiion of arsenic toxicity via MRPs in cells : 多剤耐性タンパクMRPsを介した細胞のヒ素毒性調節機構.” 2013. Thesis, Chiba University / 千葉大学. Accessed April 10, 2021. http://opac.ll.chiba-u.jp/da/curator/900118747/.

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

MLA Handbook (7th Edition):

渡辺, 喬之. “Modulatiion of arsenic toxicity via MRPs in cells : 多剤耐性タンパクMRPsを介した細胞のヒ素毒性調節機構.” 2013. Web. 10 Apr 2021.

Vancouver:

渡辺 . Modulatiion of arsenic toxicity via MRPs in cells : 多剤耐性タンパクMRPsを介した細胞のヒ素毒性調節機構. [Internet] [Thesis]. Chiba University / 千葉大学; 2013. [cited 2021 Apr 10]. Available from: http://opac.ll.chiba-u.jp/da/curator/900118747/.

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

Council of Science Editors:

渡辺 . Modulatiion of arsenic toxicity via MRPs in cells : 多剤耐性タンパクMRPsを介した細胞のヒ素毒性調節機構. [Thesis]. Chiba University / 千葉大学; 2013. Available from: http://opac.ll.chiba-u.jp/da/curator/900118747/

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


The Ohio State University

18. Park, Han-A. Natural Vitamin E, α-Tocotrienol, as a Neuroprotectant.

Degree: PhD, Human Ecology: Human Nutrition, 2010, The Ohio State University

  Natural vitamin E exists as the well known tocopherols and poorly studied tocotrienols. α-Tocotrienol (TCT) represents the most potent neuroprotective form of vitamin E.… (more)

Subjects/Keywords: Molecular Biology; Neurobiology; Nutrition; &945; -tocotrienol; glutathione disulfide; multidrug resistance-associated protein 1; stroke; 12-lipoxygenase

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APA (6th Edition):

Park, H. (2010). Natural Vitamin E, α-Tocotrienol, as a Neuroprotectant. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1291061955

Chicago Manual of Style (16th Edition):

Park, Han-A. “Natural Vitamin E, α-Tocotrienol, as a Neuroprotectant.” 2010. Doctoral Dissertation, The Ohio State University. Accessed April 10, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1291061955.

MLA Handbook (7th Edition):

Park, Han-A. “Natural Vitamin E, α-Tocotrienol, as a Neuroprotectant.” 2010. Web. 10 Apr 2021.

Vancouver:

Park H. Natural Vitamin E, α-Tocotrienol, as a Neuroprotectant. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2021 Apr 10]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1291061955.

Council of Science Editors:

Park H. Natural Vitamin E, α-Tocotrienol, as a Neuroprotectant. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1291061955


Indian Institute of Science

19. Kumar, Sushant. Structural Studies on DNA Damage Inducible Protein 1 (Ddi1) of Leishmania and the Rotavirus Nonstructural Protein NSP4.

Degree: PhD, Faculty of Science, 2018, Indian Institute of Science

 Structuraj investigations on the Ddi1 (DNA-damage inducible protein 1) of Leishmania major and on the rotavirus nonstructural protein NSP4 were carried out. Ddi1 belongs to… (more)

Subjects/Keywords: Rotavirus Nonstructural Protein NSP4; DNA Damage Inducible Protein (Ddi1); Retroviral Protease Domain (RVP); Ubiquitin-Like Domain (UBL); Ubiquitin Associated Domain (UBA); Nonstructural Protein 4; Rotavirus Strain MF66; Leishmania Major; Molecular Biophysics

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APA (6th Edition):

Kumar, S. (2018). Structural Studies on DNA Damage Inducible Protein 1 (Ddi1) of Leishmania and the Rotavirus Nonstructural Protein NSP4. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3018

Chicago Manual of Style (16th Edition):

Kumar, Sushant. “Structural Studies on DNA Damage Inducible Protein 1 (Ddi1) of Leishmania and the Rotavirus Nonstructural Protein NSP4.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed April 10, 2021. http://etd.iisc.ac.in/handle/2005/3018.

MLA Handbook (7th Edition):

Kumar, Sushant. “Structural Studies on DNA Damage Inducible Protein 1 (Ddi1) of Leishmania and the Rotavirus Nonstructural Protein NSP4.” 2018. Web. 10 Apr 2021.

Vancouver:

Kumar S. Structural Studies on DNA Damage Inducible Protein 1 (Ddi1) of Leishmania and the Rotavirus Nonstructural Protein NSP4. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2021 Apr 10]. Available from: http://etd.iisc.ac.in/handle/2005/3018.

Council of Science Editors:

Kumar S. Structural Studies on DNA Damage Inducible Protein 1 (Ddi1) of Leishmania and the Rotavirus Nonstructural Protein NSP4. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3018


University of Tasmania

20. Hoang, T. Role of the 39-kDa receptor-associated protein (RAP) in Alzheimer's disease.

Degree: 2012, University of Tasmania

 Alzheimer’s disease (AD) is the most common form of dementia that gradually worsens over time and leads to death. AD is characterized by an accumulation… (more)

Subjects/Keywords: receptor-associated protein; RAP; Alzheimer's disease

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APA (6th Edition):

Hoang, T. (2012). Role of the 39-kDa receptor-associated protein (RAP) in Alzheimer's disease. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/15010/2/whole-hoang-thesis-2012.pdf

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):

Hoang, T. “Role of the 39-kDa receptor-associated protein (RAP) in Alzheimer's disease.” 2012. Thesis, University of Tasmania. Accessed April 10, 2021. https://eprints.utas.edu.au/15010/2/whole-hoang-thesis-2012.pdf.

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

MLA Handbook (7th Edition):

Hoang, T. “Role of the 39-kDa receptor-associated protein (RAP) in Alzheimer's disease.” 2012. Web. 10 Apr 2021.

Vancouver:

Hoang T. Role of the 39-kDa receptor-associated protein (RAP) in Alzheimer's disease. [Internet] [Thesis]. University of Tasmania; 2012. [cited 2021 Apr 10]. Available from: https://eprints.utas.edu.au/15010/2/whole-hoang-thesis-2012.pdf.

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

Council of Science Editors:

Hoang T. Role of the 39-kDa receptor-associated protein (RAP) in Alzheimer's disease. [Thesis]. University of Tasmania; 2012. Available from: https://eprints.utas.edu.au/15010/2/whole-hoang-thesis-2012.pdf

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


Royal Holloway, University of London

21. Parolaro, Nathalie. The molecular composition and localization of Dystrophin-Associated Protein Complexes and ε-sarcoglycan in mammalian brain.

Degree: PhD, 2012, Royal Holloway, University of London

 Duchenne muscular dystrophies (DMD) arise from mutations in the DMD gene. In the brain, the DMD gene product, dystrophin, localizes at the post-synaptic density (PSD)… (more)

Subjects/Keywords: Dystrophin-Associated Protein Complex; epsilon sarcoglycan

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APA (6th Edition):

Parolaro, N. (2012). The molecular composition and localization of Dystrophin-Associated Protein Complexes and ε-sarcoglycan in mammalian brain. (Doctoral Dissertation). Royal Holloway, University of London. Retrieved from https://pure.royalholloway.ac.uk/portal/en/publications/the-molecular-composition-and-localization-of-dystrophinassociated-protein-complexes-and-sarcoglycan-in-mammalian-brain(1e88612e-ba63-4d02-a9d9-c615660db639).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792125

Chicago Manual of Style (16th Edition):

Parolaro, Nathalie. “The molecular composition and localization of Dystrophin-Associated Protein Complexes and ε-sarcoglycan in mammalian brain.” 2012. Doctoral Dissertation, Royal Holloway, University of London. Accessed April 10, 2021. https://pure.royalholloway.ac.uk/portal/en/publications/the-molecular-composition-and-localization-of-dystrophinassociated-protein-complexes-and-sarcoglycan-in-mammalian-brain(1e88612e-ba63-4d02-a9d9-c615660db639).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792125.

MLA Handbook (7th Edition):

Parolaro, Nathalie. “The molecular composition and localization of Dystrophin-Associated Protein Complexes and ε-sarcoglycan in mammalian brain.” 2012. Web. 10 Apr 2021.

Vancouver:

Parolaro N. The molecular composition and localization of Dystrophin-Associated Protein Complexes and ε-sarcoglycan in mammalian brain. [Internet] [Doctoral dissertation]. Royal Holloway, University of London; 2012. [cited 2021 Apr 10]. Available from: https://pure.royalholloway.ac.uk/portal/en/publications/the-molecular-composition-and-localization-of-dystrophinassociated-protein-complexes-and-sarcoglycan-in-mammalian-brain(1e88612e-ba63-4d02-a9d9-c615660db639).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792125.

Council of Science Editors:

Parolaro N. The molecular composition and localization of Dystrophin-Associated Protein Complexes and ε-sarcoglycan in mammalian brain. [Doctoral Dissertation]. Royal Holloway, University of London; 2012. Available from: https://pure.royalholloway.ac.uk/portal/en/publications/the-molecular-composition-and-localization-of-dystrophinassociated-protein-complexes-and-sarcoglycan-in-mammalian-brain(1e88612e-ba63-4d02-a9d9-c615660db639).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.792125


University of Missouri – Columbia

22. Spreng, Krista A. Identification and characterization of Bacillus anthracis spore-associated proteins.

Degree: 2012, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Bacillus anthracis is a Gram-positive, rod-shaped, spore-forming bacterium and the etiological agent of anthrax. Spore… (more)

Subjects/Keywords: anthrax; sporulation process; exosporium; spore-associated protein

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APA (6th Edition):

Spreng, K. A. (2012). Identification and characterization of Bacillus anthracis spore-associated proteins. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/15193

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):

Spreng, Krista A. “Identification and characterization of Bacillus anthracis spore-associated proteins.” 2012. Thesis, University of Missouri – Columbia. Accessed April 10, 2021. https://doi.org/10.32469/10355/15193.

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

MLA Handbook (7th Edition):

Spreng, Krista A. “Identification and characterization of Bacillus anthracis spore-associated proteins.” 2012. Web. 10 Apr 2021.

Vancouver:

Spreng KA. Identification and characterization of Bacillus anthracis spore-associated proteins. [Internet] [Thesis]. University of Missouri – Columbia; 2012. [cited 2021 Apr 10]. Available from: https://doi.org/10.32469/10355/15193.

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

Council of Science Editors:

Spreng KA. Identification and characterization of Bacillus anthracis spore-associated proteins. [Thesis]. University of Missouri – Columbia; 2012. Available from: https://doi.org/10.32469/10355/15193

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


Universiteit Utrecht

23. Laffont, Céline Marielle. Factors Affecting the Disposition of Ivermectin in the Target Species.

Degree: 2002, Universiteit Utrecht

 It was the aim of the thesis to contribute to the understanding of the diverse factors involved in the pharmacokinetics of ivermectin, a very potent… (more)

Subjects/Keywords: Diergeneeskunde; ivermectin; intestinal secretion; faecal elimination; P-glycoprotein (P-gp); multidrug resistance-associated protein 2 (MRP2); rat intestinal loops; Caco-2 cells; licking behaviour; endectocide

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APA (6th Edition):

Laffont, C. M. (2002). Factors Affecting the Disposition of Ivermectin in the Target Species. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/292

Chicago Manual of Style (16th Edition):

Laffont, Céline Marielle. “Factors Affecting the Disposition of Ivermectin in the Target Species.” 2002. Doctoral Dissertation, Universiteit Utrecht. Accessed April 10, 2021. http://dspace.library.uu.nl:8080/handle/1874/292.

MLA Handbook (7th Edition):

Laffont, Céline Marielle. “Factors Affecting the Disposition of Ivermectin in the Target Species.” 2002. Web. 10 Apr 2021.

Vancouver:

Laffont CM. Factors Affecting the Disposition of Ivermectin in the Target Species. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2002. [cited 2021 Apr 10]. Available from: http://dspace.library.uu.nl:8080/handle/1874/292.

Council of Science Editors:

Laffont CM. Factors Affecting the Disposition of Ivermectin in the Target Species. [Doctoral Dissertation]. Universiteit Utrecht; 2002. Available from: http://dspace.library.uu.nl:8080/handle/1874/292

24. Laffont, Céline Marielle. Factors Affecting the Disposition of Ivermectin in the Target Species.

Degree: 2002, University Utrecht

 It was the aim of the thesis to contribute to the understanding of the diverse factors involved in the pharmacokinetics of ivermectin, a very potent… (more)

Subjects/Keywords: ivermectin; intestinal secretion; faecal elimination; P-glycoprotein (P-gp); multidrug resistance-associated protein 2 (MRP2); rat intestinal loops; Caco-2 cells; licking behaviour; endectocide

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APA (6th Edition):

Laffont, C. M. (2002). Factors Affecting the Disposition of Ivermectin in the Target Species. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/292 ; URN:NBN:NL:UI:10-1874-292 ; 1874/292 ; URN:NBN:NL:UI:10-1874-292 ; https://dspace.library.uu.nl/handle/1874/292

Chicago Manual of Style (16th Edition):

Laffont, Céline Marielle. “Factors Affecting the Disposition of Ivermectin in the Target Species.” 2002. Doctoral Dissertation, University Utrecht. Accessed April 10, 2021. https://dspace.library.uu.nl/handle/1874/292 ; URN:NBN:NL:UI:10-1874-292 ; 1874/292 ; URN:NBN:NL:UI:10-1874-292 ; https://dspace.library.uu.nl/handle/1874/292.

MLA Handbook (7th Edition):

Laffont, Céline Marielle. “Factors Affecting the Disposition of Ivermectin in the Target Species.” 2002. Web. 10 Apr 2021.

Vancouver:

Laffont CM. Factors Affecting the Disposition of Ivermectin in the Target Species. [Internet] [Doctoral dissertation]. University Utrecht; 2002. [cited 2021 Apr 10]. Available from: https://dspace.library.uu.nl/handle/1874/292 ; URN:NBN:NL:UI:10-1874-292 ; 1874/292 ; URN:NBN:NL:UI:10-1874-292 ; https://dspace.library.uu.nl/handle/1874/292.

Council of Science Editors:

Laffont CM. Factors Affecting the Disposition of Ivermectin in the Target Species. [Doctoral Dissertation]. University Utrecht; 2002. Available from: https://dspace.library.uu.nl/handle/1874/292 ; URN:NBN:NL:UI:10-1874-292 ; 1874/292 ; URN:NBN:NL:UI:10-1874-292 ; https://dspace.library.uu.nl/handle/1874/292


University of Manitoba

25. 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 10, 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. 10 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 10]. 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


Texas Tech University

26. Swartz, Douglas. Genetic manipulation of P-glycoprotein provides new tools for biophysical studies of the ABC multidrug transport mechanism.

Degree: TTUHSC  – Biochemistry and Molecular Genetics, 2012, Texas Tech University

 P-glycoprotein (Pgp) is an ATP Binding Cassette (ABC) transporter that functions as a multidrug efflux pump, and contributes to multidrug resistance in cancer and other… (more)

Subjects/Keywords: P-gloycoprotein; Membrane protein; ATP binding cassette (ABC) transporter; Multidrug transporter

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APA (6th Edition):

Swartz, D. (2012). Genetic manipulation of P-glycoprotein provides new tools for biophysical studies of the ABC multidrug transport mechanism. (Thesis). Texas Tech University. Retrieved from http://hdl.handle.net/2346/47087

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):

Swartz, Douglas. “Genetic manipulation of P-glycoprotein provides new tools for biophysical studies of the ABC multidrug transport mechanism.” 2012. Thesis, Texas Tech University. Accessed April 10, 2021. http://hdl.handle.net/2346/47087.

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

MLA Handbook (7th Edition):

Swartz, Douglas. “Genetic manipulation of P-glycoprotein provides new tools for biophysical studies of the ABC multidrug transport mechanism.” 2012. Web. 10 Apr 2021.

Vancouver:

Swartz D. Genetic manipulation of P-glycoprotein provides new tools for biophysical studies of the ABC multidrug transport mechanism. [Internet] [Thesis]. Texas Tech University; 2012. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/2346/47087.

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

Council of Science Editors:

Swartz D. Genetic manipulation of P-glycoprotein provides new tools for biophysical studies of the ABC multidrug transport mechanism. [Thesis]. Texas Tech University; 2012. Available from: http://hdl.handle.net/2346/47087

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


Queens University

27. 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 10, 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. 10 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 10]. 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


Australian National University

28. Carey Hulyer, Alex Robert. Bioenergetic coupling in P-glycoprotein: determining the relative position, topography and role of transmembrane helices six and twelve .

Degree: 2018, Australian National University

Multidrug efflux pump P-glycoprotein (P-gp) has been the subject of significant research interest since the discovery of the protein in multi-drug resistant cancer cells 40… (more)

Subjects/Keywords: P-glycoprotein; Multidrug-efflux; Cancer; Chemotherapy; Membrane Protein; Biochemistry; Cross-linking

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APA (6th Edition):

Carey Hulyer, A. R. (2018). Bioenergetic coupling in P-glycoprotein: determining the relative position, topography and role of transmembrane helices six and twelve . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/156454

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):

Carey Hulyer, Alex Robert. “Bioenergetic coupling in P-glycoprotein: determining the relative position, topography and role of transmembrane helices six and twelve .” 2018. Thesis, Australian National University. Accessed April 10, 2021. http://hdl.handle.net/1885/156454.

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

MLA Handbook (7th Edition):

Carey Hulyer, Alex Robert. “Bioenergetic coupling in P-glycoprotein: determining the relative position, topography and role of transmembrane helices six and twelve .” 2018. Web. 10 Apr 2021.

Vancouver:

Carey Hulyer AR. Bioenergetic coupling in P-glycoprotein: determining the relative position, topography and role of transmembrane helices six and twelve . [Internet] [Thesis]. Australian National University; 2018. [cited 2021 Apr 10]. Available from: http://hdl.handle.net/1885/156454.

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

Council of Science Editors:

Carey Hulyer AR. Bioenergetic coupling in P-glycoprotein: determining the relative position, topography and role of transmembrane helices six and twelve . [Thesis]. Australian National University; 2018. Available from: http://hdl.handle.net/1885/156454

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


University of Kentucky

29. 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 10, 2021. https://uknowledge.uky.edu/chemistry_etds/33.

MLA Handbook (7th Edition):

Ye, Cui. “STABILITY STUDIES OF MEMBRANE PROTEINS.” 2014. Web. 10 Apr 2021.

Vancouver:

Ye C. STABILITY STUDIES OF MEMBRANE PROTEINS. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2021 Apr 10]. 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


University of Western Ontario

30. Knauer, Michael J. The Role of Drug Transporters in Statin-Induced Myopathy.

Degree: 2012, University of Western Ontario

 Statins are the first line therapy for treatment and prevention of cardiovascular disease. The 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitors, or statins, reduce plasma cholesterol levels… (more)

Subjects/Keywords: Organic anion transporting polypeptides; multidrug resistant associated proteins; drug transporter; statins; statin transport; statin pharmacokinetics; statin myopathy; Pharmacology

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

APA (6th Edition):

Knauer, M. J. (2012). The Role of Drug Transporters in Statin-Induced Myopathy. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1001

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):

Knauer, Michael J. “The Role of Drug Transporters in Statin-Induced Myopathy.” 2012. Thesis, University of Western Ontario. Accessed April 10, 2021. https://ir.lib.uwo.ca/etd/1001.

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

MLA Handbook (7th Edition):

Knauer, Michael J. “The Role of Drug Transporters in Statin-Induced Myopathy.” 2012. Web. 10 Apr 2021.

Vancouver:

Knauer MJ. The Role of Drug Transporters in Statin-Induced Myopathy. [Internet] [Thesis]. University of Western Ontario; 2012. [cited 2021 Apr 10]. Available from: https://ir.lib.uwo.ca/etd/1001.

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

Council of Science Editors:

Knauer MJ. The Role of Drug Transporters in Statin-Induced Myopathy. [Thesis]. University of Western Ontario; 2012. Available from: https://ir.lib.uwo.ca/etd/1001

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

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