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You searched for subject:(MRP4). Showing records 1 – 13 of 13 total matches.

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University of California – San Francisco

1. Friedman, Jessica Lauren. Effect of ABCC4 Genetic Variation on MRP4 ATPase Activity.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2015, University of California – San Francisco

 ATP-binding cassette (ABC) transporters are a diverse family of transmembrane proteins that facilitate the ATP powered translocation of substrates across cellular membranes. Multidrug resistance-associated protein… (more)

Subjects/Keywords: Pharmaceutical sciences; Biochemistry; ABC transporter; MRP4

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APA (6th Edition):

Friedman, J. L. (2015). Effect of ABCC4 Genetic Variation on MRP4 ATPase Activity. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7xv9f7fb

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):

Friedman, Jessica Lauren. “Effect of ABCC4 Genetic Variation on MRP4 ATPase Activity.” 2015. Thesis, University of California – San Francisco. Accessed March 06, 2021. http://www.escholarship.org/uc/item/7xv9f7fb.

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

MLA Handbook (7th Edition):

Friedman, Jessica Lauren. “Effect of ABCC4 Genetic Variation on MRP4 ATPase Activity.” 2015. Web. 06 Mar 2021.

Vancouver:

Friedman JL. Effect of ABCC4 Genetic Variation on MRP4 ATPase Activity. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/7xv9f7fb.

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

Council of Science Editors:

Friedman JL. Effect of ABCC4 Genetic Variation on MRP4 ATPase Activity. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/7xv9f7fb

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

2. Carozzo, Alejandro Enrique. Estudio de los mecanismos de regulación de la proteína asociada a resistencia a multidrogas 4 (MRP4) y sus implicancias en adenocarcinomas ductales pancreáticos.

Degree: Farmacia y Bioquímica, 2015, Universidad de Buenos Aires

Pancreatic ductal adenocarcinoma (PDAC), the most common histological subtype of pancreatic cancer, is one of the most lethal human cancers, representing the fourth leading cause… (more)

Subjects/Keywords: AMPc; Páncreas; Diferenciación; MRP4; Ciencia de la vida

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APA (6th Edition):

Carozzo, A. E. (2015). Estudio de los mecanismos de regulación de la proteína asociada a resistencia a multidrogas 4 (MRP4) y sus implicancias en adenocarcinomas ductales pancreáticos. (Thesis). Universidad de Buenos Aires. Retrieved from http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1133 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1133.dir/1133.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):

Carozzo, Alejandro Enrique. “Estudio de los mecanismos de regulación de la proteína asociada a resistencia a multidrogas 4 (MRP4) y sus implicancias en adenocarcinomas ductales pancreáticos.” 2015. Thesis, Universidad de Buenos Aires. Accessed March 06, 2021. http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1133 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1133.dir/1133.PDF.

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

MLA Handbook (7th Edition):

Carozzo, Alejandro Enrique. “Estudio de los mecanismos de regulación de la proteína asociada a resistencia a multidrogas 4 (MRP4) y sus implicancias en adenocarcinomas ductales pancreáticos.” 2015. Web. 06 Mar 2021.

Vancouver:

Carozzo AE. Estudio de los mecanismos de regulación de la proteína asociada a resistencia a multidrogas 4 (MRP4) y sus implicancias en adenocarcinomas ductales pancreáticos. [Internet] [Thesis]. Universidad de Buenos Aires; 2015. [cited 2021 Mar 06]. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1133 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1133.dir/1133.PDF.

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

Council of Science Editors:

Carozzo AE. Estudio de los mecanismos de regulación de la proteína asociada a resistencia a multidrogas 4 (MRP4) y sus implicancias en adenocarcinomas ductales pancreáticos. [Thesis]. Universidad de Buenos Aires; 2015. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1133 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1133.dir/1133.PDF

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

3. NEO WEE LOONG, THOMAS. The transcriptional regulation of human multidrug resistance associated protein 4 gene expression by xenobiotics.

Degree: 2008, National University of Singapore

Subjects/Keywords: Transcriptional Regulation MRP4 Xenobiotics

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APA (6th Edition):

NEO WEE LOONG, T. (2008). The transcriptional regulation of human multidrug resistance associated protein 4 gene expression by xenobiotics. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/16101

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):

NEO WEE LOONG, THOMAS. “The transcriptional regulation of human multidrug resistance associated protein 4 gene expression by xenobiotics.” 2008. Thesis, National University of Singapore. Accessed March 06, 2021. http://scholarbank.nus.edu.sg/handle/10635/16101.

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

MLA Handbook (7th Edition):

NEO WEE LOONG, THOMAS. “The transcriptional regulation of human multidrug resistance associated protein 4 gene expression by xenobiotics.” 2008. Web. 06 Mar 2021.

Vancouver:

NEO WEE LOONG T. The transcriptional regulation of human multidrug resistance associated protein 4 gene expression by xenobiotics. [Internet] [Thesis]. National University of Singapore; 2008. [cited 2021 Mar 06]. Available from: http://scholarbank.nus.edu.sg/handle/10635/16101.

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

Council of Science Editors:

NEO WEE LOONG T. The transcriptional regulation of human multidrug resistance associated protein 4 gene expression by xenobiotics. [Thesis]. National University of Singapore; 2008. Available from: http://scholarbank.nus.edu.sg/handle/10635/16101

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


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 March 06, 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. 06 Mar 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 Mar 06]. 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


Texas State University – San Marcos

5. 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 March 06, 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. 06 Mar 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 Mar 06]. 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

6. 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 March 06, 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. 06 Mar 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 Mar 06]. 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

7. 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 March 06, 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. 06 Mar 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 Mar 06]. 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

8. YANG FEI. Effects of novel purine analogs and the role of aromatic amino acids on MRP4 functions.

Degree: 2005, National University of Singapore

Subjects/Keywords: MRP; MRP4; bimane-GS efflux; resistance to 6-TG; aromatic amino acid

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APA (6th Edition):

FEI, Y. (2005). Effects of novel purine analogs and the role of aromatic amino acids on MRP4 functions. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/15016

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):

FEI, YANG. “Effects of novel purine analogs and the role of aromatic amino acids on MRP4 functions.” 2005. Thesis, National University of Singapore. Accessed March 06, 2021. http://scholarbank.nus.edu.sg/handle/10635/15016.

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

MLA Handbook (7th Edition):

FEI, YANG. “Effects of novel purine analogs and the role of aromatic amino acids on MRP4 functions.” 2005. Web. 06 Mar 2021.

Vancouver:

FEI Y. Effects of novel purine analogs and the role of aromatic amino acids on MRP4 functions. [Internet] [Thesis]. National University of Singapore; 2005. [cited 2021 Mar 06]. Available from: http://scholarbank.nus.edu.sg/handle/10635/15016.

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

Council of Science Editors:

FEI Y. Effects of novel purine analogs and the role of aromatic amino acids on MRP4 functions. [Thesis]. National University of Singapore; 2005. Available from: http://scholarbank.nus.edu.sg/handle/10635/15016

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

9. 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 March 06, 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. 06 Mar 2021.

Vancouver:

QUAN T. Interactions of human multidrug resistance protein 4 with camptothecins. [Internet] [Thesis]. National University of Singapore; 2009. [cited 2021 Mar 06]. 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

10. Morgan, Jessica Ann. Mrp4 Is a Crucial Regulator of Testosterone Biosynthesis.

Degree: PhD, Biomedical Sciences, 2012, University of Tennessee Health Science Center

  The physiological role of multidrug resistance protein 4 (Mrp4) in the testes is unknown. It was discovered that Mrp4 is expressed primarily in mouse… (more)

Subjects/Keywords: cAMP; testosterone; Mrp4; Leydig cell; Amino Acids, Peptides, and Proteins; Chemicals and Drugs; Medical Cell Biology; Medical Sciences; Medicine and Health Sciences

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APA (6th Edition):

Morgan, J. A. (2012). Mrp4 Is a Crucial Regulator of Testosterone Biosynthesis. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/182

Chicago Manual of Style (16th Edition):

Morgan, Jessica Ann. “Mrp4 Is a Crucial Regulator of Testosterone Biosynthesis.” 2012. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed March 06, 2021. https://dc.uthsc.edu/dissertations/182.

MLA Handbook (7th Edition):

Morgan, Jessica Ann. “Mrp4 Is a Crucial Regulator of Testosterone Biosynthesis.” 2012. Web. 06 Mar 2021.

Vancouver:

Morgan JA. Mrp4 Is a Crucial Regulator of Testosterone Biosynthesis. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2012. [cited 2021 Mar 06]. Available from: https://dc.uthsc.edu/dissertations/182.

Council of Science Editors:

Morgan JA. Mrp4 Is a Crucial Regulator of Testosterone Biosynthesis. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2012. Available from: https://dc.uthsc.edu/dissertations/182

11. Sinha, Chandrima. MRP4-Dependent Regulation of Fibroblast Migration.

Degree: PhD, Biomedical Sciences, 2014, University of Tennessee Health Science Center

  Roles of cyclic nucleotides and cyclic nucleotide-dependent signaling molecules in regulating several signaling pathways including cell migration have long been known. However, the new… (more)

Subjects/Keywords: Actin; Cyclic nucleotides; Fibroblasts; Migration; MRP4; PKA; Chemicals and Drugs; Medical Biochemistry; Medical Cell Biology; Medical Sciences; Medicine and Health Sciences; Nucleic Acids, Nucleotides, and Nucleosides

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APA (6th Edition):

Sinha, C. (2014). MRP4-Dependent Regulation of Fibroblast Migration. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/248

Chicago Manual of Style (16th Edition):

Sinha, Chandrima. “MRP4-Dependent Regulation of Fibroblast Migration.” 2014. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed March 06, 2021. https://dc.uthsc.edu/dissertations/248.

MLA Handbook (7th Edition):

Sinha, Chandrima. “MRP4-Dependent Regulation of Fibroblast Migration.” 2014. Web. 06 Mar 2021.

Vancouver:

Sinha C. MRP4-Dependent Regulation of Fibroblast Migration. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2014. [cited 2021 Mar 06]. Available from: https://dc.uthsc.edu/dissertations/248.

Council of Science Editors:

Sinha C. MRP4-Dependent Regulation of Fibroblast Migration. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2014. Available from: https://dc.uthsc.edu/dissertations/248


University of Southern California

12. Bi, Lucun. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.

Degree: PhD, Pharmaceutical Sciences, 2008, University of Southern California

 High level of virologic failure was observed in HIV patients receiving combinations of tenofovir (TFV), lamivudine (3TC) combined with either abacavir (ABC) or didanosine (ddI).… (more)

Subjects/Keywords: nucleoside analog; NRTI; intracellular drug-drug interaction; efflux transporters; MRP2; MRP4; cellular adaptive response; ddNTP; TFV; ABC; ddI; endogenous nucleotide pools; PNP

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APA (6th Edition):

Bi, L. (2008). Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609

Chicago Manual of Style (16th Edition):

Bi, Lucun. “Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 06, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609.

MLA Handbook (7th Edition):

Bi, Lucun. “Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.” 2008. Web. 06 Mar 2021.

Vancouver:

Bi L. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 06]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609.

Council of Science Editors:

Bi L. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609

13. Turner, Patricia Kellie. The Role of Multi-Drug Resistance Associated Protein 4 and P-glycoprotein in Resistance of Neuroblastoma to Topotecan and Irinotecan.

Degree: PhD, Pharmaceutical Sciences, 2007, University of Tennessee Health Science Center

  High-risk neuroblastoma presents a significant therapeutic challenge because the 5-year survival rate remains less than 30% despite the use of surgery, multi-agent chemotherapy, radiation,… (more)

Subjects/Keywords: Neuroblastoma; topotecan; irinotecan; ABC transporter; multidrug resistance; MRP4; Pgp; RNAi; shRNA; siRNA; immunohistochemistry; Amino Acids, Peptides, and Proteins; Chemicals and Drugs; Diseases; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Neoplasms; Pharmaceutical Preparations; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Turner, P. K. (2007). The Role of Multi-Drug Resistance Associated Protein 4 and P-glycoprotein in Resistance of Neuroblastoma to Topotecan and Irinotecan. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/269

Chicago Manual of Style (16th Edition):

Turner, Patricia Kellie. “The Role of Multi-Drug Resistance Associated Protein 4 and P-glycoprotein in Resistance of Neuroblastoma to Topotecan and Irinotecan.” 2007. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed March 06, 2021. https://dc.uthsc.edu/dissertations/269.

MLA Handbook (7th Edition):

Turner, Patricia Kellie. “The Role of Multi-Drug Resistance Associated Protein 4 and P-glycoprotein in Resistance of Neuroblastoma to Topotecan and Irinotecan.” 2007. Web. 06 Mar 2021.

Vancouver:

Turner PK. The Role of Multi-Drug Resistance Associated Protein 4 and P-glycoprotein in Resistance of Neuroblastoma to Topotecan and Irinotecan. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2007. [cited 2021 Mar 06]. Available from: https://dc.uthsc.edu/dissertations/269.

Council of Science Editors:

Turner PK. The Role of Multi-Drug Resistance Associated Protein 4 and P-glycoprotein in Resistance of Neuroblastoma to Topotecan and Irinotecan. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2007. Available from: https://dc.uthsc.edu/dissertations/269

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