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You searched for subject:(Liposome). Showing records 1 – 30 of 223 total matches.

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Dalhousie University

1. Li, Zhiyu. ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES.

Degree: MS, Department of Process Engineering and Applied Science, 2014, Dalhousie University

 Bioactive low molecular weight protein hydrolysates need to be protected, transported to the targeted absorption site, and released in a controlled manner to optimize their… (more)

Subjects/Keywords: Encapsulation; Liposome; Chitosan; Protein hydrolysates

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APA (6th Edition):

Li, Z. (2014). ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/54045

Chicago Manual of Style (16th Edition):

Li, Zhiyu. “ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES.” 2014. Masters Thesis, Dalhousie University. Accessed June 20, 2019. http://hdl.handle.net/10222/54045.

MLA Handbook (7th Edition):

Li, Zhiyu. “ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES.” 2014. Web. 20 Jun 2019.

Vancouver:

Li Z. ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10222/54045.

Council of Science Editors:

Li Z. ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES. [Masters Thesis]. Dalhousie University; 2014. Available from: http://hdl.handle.net/10222/54045


University of Alberta

2. Mahmoud, Maysoon. Liposome-based therapy: An alternative approach to treat Helicobacter pylori infection in high prevalence communities such as Aklavik, NWT.

Degree: PhD, Medical Sciences-Laboratory Medicine and Pathology, 2015, University of Alberta

 Helicobacter pylori infects about half of the world population causing chronic gastritis, peptic ulcer or gastric cancer. The Aboriginal people in Aklavik, NWT, Canada are… (more)

Subjects/Keywords: Helicobacter pylori; Liposome; Aklavik

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APA (6th Edition):

Mahmoud, M. (2015). Liposome-based therapy: An alternative approach to treat Helicobacter pylori infection in high prevalence communities such as Aklavik, NWT. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/cz890rt24h

Chicago Manual of Style (16th Edition):

Mahmoud, Maysoon. “Liposome-based therapy: An alternative approach to treat Helicobacter pylori infection in high prevalence communities such as Aklavik, NWT.” 2015. Doctoral Dissertation, University of Alberta. Accessed June 20, 2019. https://era.library.ualberta.ca/files/cz890rt24h.

MLA Handbook (7th Edition):

Mahmoud, Maysoon. “Liposome-based therapy: An alternative approach to treat Helicobacter pylori infection in high prevalence communities such as Aklavik, NWT.” 2015. Web. 20 Jun 2019.

Vancouver:

Mahmoud M. Liposome-based therapy: An alternative approach to treat Helicobacter pylori infection in high prevalence communities such as Aklavik, NWT. [Internet] [Doctoral dissertation]. University of Alberta; 2015. [cited 2019 Jun 20]. Available from: https://era.library.ualberta.ca/files/cz890rt24h.

Council of Science Editors:

Mahmoud M. Liposome-based therapy: An alternative approach to treat Helicobacter pylori infection in high prevalence communities such as Aklavik, NWT. [Doctoral Dissertation]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/cz890rt24h


Penn State University

3. Sutermaster, Bryan A. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.

Degree: MS, Bioengineering, 2012, Penn State University

 Nanoliposomes continue to be an interesting candidate for overcoming disadvantages in conventional systemic drug delivery, including off-target toxicities and short circulation times. Various modifications, like… (more)

Subjects/Keywords: liposome; siRNA; cancer; drug delivery

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APA (6th Edition):

Sutermaster, B. A. (2012). Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/15235

Chicago Manual of Style (16th Edition):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Masters Thesis, Penn State University. Accessed June 20, 2019. https://etda.libraries.psu.edu/catalog/15235.

MLA Handbook (7th Edition):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Web. 20 Jun 2019.

Vancouver:

Sutermaster BA. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. [Internet] [Masters thesis]. Penn State University; 2012. [cited 2019 Jun 20]. Available from: https://etda.libraries.psu.edu/catalog/15235.

Council of Science Editors:

Sutermaster BA. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. [Masters Thesis]. Penn State University; 2012. Available from: https://etda.libraries.psu.edu/catalog/15235


Louisiana State University

4. Chanda, Dipon. Liposomal uptake of silver and gold nanoparticles.

Degree: MSME, Mechanical Engineering, 2013, Louisiana State University

 The main objective of this work is to study the liposomal uptake of silver and old nanoparticles. Liposomes were prepared in Heating Method. The phospholipids… (more)

Subjects/Keywords: Liposome; Nanoparticle; Heating Method

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APA (6th Edition):

Chanda, D. (2013). Liposomal uptake of silver and gold nanoparticles. (Masters Thesis). Louisiana State University. Retrieved from etd-07082013-094604 ; https://digitalcommons.lsu.edu/gradschool_theses/1821

Chicago Manual of Style (16th Edition):

Chanda, Dipon. “Liposomal uptake of silver and gold nanoparticles.” 2013. Masters Thesis, Louisiana State University. Accessed June 20, 2019. etd-07082013-094604 ; https://digitalcommons.lsu.edu/gradschool_theses/1821.

MLA Handbook (7th Edition):

Chanda, Dipon. “Liposomal uptake of silver and gold nanoparticles.” 2013. Web. 20 Jun 2019.

Vancouver:

Chanda D. Liposomal uptake of silver and gold nanoparticles. [Internet] [Masters thesis]. Louisiana State University; 2013. [cited 2019 Jun 20]. Available from: etd-07082013-094604 ; https://digitalcommons.lsu.edu/gradschool_theses/1821.

Council of Science Editors:

Chanda D. Liposomal uptake of silver and gold nanoparticles. [Masters Thesis]. Louisiana State University; 2013. Available from: etd-07082013-094604 ; https://digitalcommons.lsu.edu/gradschool_theses/1821


University of Saskatchewan

5. Rutherford, Hayley. Structural investigations of liposomes: effect of phospholipid hydrocarbon length and incorporation of sphingomyelin.

Degree: 2011, University of Saskatchewan

 The liquid crystal morphologies of symmetrical diacyl phosphatidylcholine liposomes examined in this research were found to be dependent on saturated hydrocarbon chain length. Both powder… (more)

Subjects/Keywords: liposome; phospholipid; supramolecular structure

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APA (6th Edition):

Rutherford, H. (2011). Structural investigations of liposomes: effect of phospholipid hydrocarbon length and incorporation of sphingomyelin. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-08-148

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):

Rutherford, Hayley. “Structural investigations of liposomes: effect of phospholipid hydrocarbon length and incorporation of sphingomyelin.” 2011. Thesis, University of Saskatchewan. Accessed June 20, 2019. http://hdl.handle.net/10388/ETD-2011-08-148.

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

MLA Handbook (7th Edition):

Rutherford, Hayley. “Structural investigations of liposomes: effect of phospholipid hydrocarbon length and incorporation of sphingomyelin.” 2011. Web. 20 Jun 2019.

Vancouver:

Rutherford H. Structural investigations of liposomes: effect of phospholipid hydrocarbon length and incorporation of sphingomyelin. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/10388/ETD-2011-08-148.

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

Council of Science Editors:

Rutherford H. Structural investigations of liposomes: effect of phospholipid hydrocarbon length and incorporation of sphingomyelin. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-08-148

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


Cornell University

6. Tsai, Wen-Chyan. Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process .

Degree: 2015, Cornell University

 A novel supercritical fluid (SCF) process, composed of SCF extraction, rapid expansion of a supercritical solution, and vacuum-driven cargo loading based on the Bernoulli principle,… (more)

Subjects/Keywords: supercritical carbon dioxide; liposome; microencapsulation

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APA (6th Edition):

Tsai, W. (2015). Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/41168

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):

Tsai, Wen-Chyan. “Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process .” 2015. Thesis, Cornell University. Accessed June 20, 2019. http://hdl.handle.net/1813/41168.

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

MLA Handbook (7th Edition):

Tsai, Wen-Chyan. “Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process .” 2015. Web. 20 Jun 2019.

Vancouver:

Tsai W. Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process . [Internet] [Thesis]. Cornell University; 2015. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1813/41168.

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

Council of Science Editors:

Tsai W. Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process . [Thesis]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41168

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


University of Notre Dame

7. Victoria Elizabeth Froude. AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>.

Degree: PhD, Chemical Engineering, 2011, University of Notre Dame

  Recently, lipid based biocolloids, such as micelles and liposomes, have been of increasing interest as drug delivery systems for controlled release, specific cell targeting,… (more)

Subjects/Keywords: Electroformation; Liposome; Dielectrophoresis; Micelle

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APA (6th Edition):

Froude, V. E. (2011). AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/pc289g5791g

Chicago Manual of Style (16th Edition):

Froude, Victoria Elizabeth. “AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>.” 2011. Doctoral Dissertation, University of Notre Dame. Accessed June 20, 2019. https://curate.nd.edu/show/pc289g5791g.

MLA Handbook (7th Edition):

Froude, Victoria Elizabeth. “AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>.” 2011. Web. 20 Jun 2019.

Vancouver:

Froude VE. AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2011. [cited 2019 Jun 20]. Available from: https://curate.nd.edu/show/pc289g5791g.

Council of Science Editors:

Froude VE. AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>. [Doctoral Dissertation]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/pc289g5791g


University of California – San Francisco

8. Perttu, Emily. The Effect of Lipid Chemistry and Structure on Liposome Formation.

Degree: Bioengineering, 2012, University of California – San Francisco

 Lipids have been known to self-assemble into vesicles for over four decades; a process that has been exploited in fields ranging from drug delivery to… (more)

Subjects/Keywords: Chemistry; Drug Delivery; Lipid; Liposome

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APA (6th Edition):

Perttu, E. (2012). The Effect of Lipid Chemistry and Structure on Liposome Formation. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/11w3j6k2

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):

Perttu, Emily. “The Effect of Lipid Chemistry and Structure on Liposome Formation.” 2012. Thesis, University of California – San Francisco. Accessed June 20, 2019. http://www.escholarship.org/uc/item/11w3j6k2.

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

MLA Handbook (7th Edition):

Perttu, Emily. “The Effect of Lipid Chemistry and Structure on Liposome Formation.” 2012. Web. 20 Jun 2019.

Vancouver:

Perttu E. The Effect of Lipid Chemistry and Structure on Liposome Formation. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Jun 20]. Available from: http://www.escholarship.org/uc/item/11w3j6k2.

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

Council of Science Editors:

Perttu E. The Effect of Lipid Chemistry and Structure on Liposome Formation. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/11w3j6k2

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

9. Chen, Su. Photothérapie dynamique vectorisée contre le rétinoblastome : conception, Synthèse et Etudes photobiologiques de photosensibilisateurs excitables à deux photons : Synthesis and Photobiological Evaluations of Porphyrine Dimers for Targeted Two-Photon Photodynamic Therapy.

Degree: Docteur es, Chimie, 2016, Paris Saclay

La photothérapie dynamique (PDT) est un nouveau traitement n’induisant potentiellement pas de mutation et utilisable pour lutter contre le rétinoblastome. Les dérivés de porphyrine utilisés… (more)

Subjects/Keywords: Pdt-Adp; Rétinoblastome; Liposome; 2pa-Pdt; Retinoblastoma; Liposome

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APA (6th Edition):

Chen, S. (2016). Photothérapie dynamique vectorisée contre le rétinoblastome : conception, Synthèse et Etudes photobiologiques de photosensibilisateurs excitables à deux photons : Synthesis and Photobiological Evaluations of Porphyrine Dimers for Targeted Two-Photon Photodynamic Therapy. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLS031

Chicago Manual of Style (16th Edition):

Chen, Su. “Photothérapie dynamique vectorisée contre le rétinoblastome : conception, Synthèse et Etudes photobiologiques de photosensibilisateurs excitables à deux photons : Synthesis and Photobiological Evaluations of Porphyrine Dimers for Targeted Two-Photon Photodynamic Therapy.” 2016. Doctoral Dissertation, Paris Saclay. Accessed June 20, 2019. http://www.theses.fr/2016SACLS031.

MLA Handbook (7th Edition):

Chen, Su. “Photothérapie dynamique vectorisée contre le rétinoblastome : conception, Synthèse et Etudes photobiologiques de photosensibilisateurs excitables à deux photons : Synthesis and Photobiological Evaluations of Porphyrine Dimers for Targeted Two-Photon Photodynamic Therapy.” 2016. Web. 20 Jun 2019.

Vancouver:

Chen S. Photothérapie dynamique vectorisée contre le rétinoblastome : conception, Synthèse et Etudes photobiologiques de photosensibilisateurs excitables à deux photons : Synthesis and Photobiological Evaluations of Porphyrine Dimers for Targeted Two-Photon Photodynamic Therapy. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2016SACLS031.

Council of Science Editors:

Chen S. Photothérapie dynamique vectorisée contre le rétinoblastome : conception, Synthèse et Etudes photobiologiques de photosensibilisateurs excitables à deux photons : Synthesis and Photobiological Evaluations of Porphyrine Dimers for Targeted Two-Photon Photodynamic Therapy. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLS031

10. Borborema, Samanta Etel Treiger. Desenvolvimento e farmacocinética de antimônio encapsulado em lipossomas de fosfatidilserina utilizando radioisótopos em leishmaniose experimental.

Degree: PhD, Tecnologia Nuclear - Aplicações, 2010, University of São Paulo

Leishmanioses são um complexo de doenças infecciosas causadas por protozoários intramacrofágicos do gênero Leishmania, fatal se não tratadas adequadamente. Os antimoniais pentavalentes são os medicamentos… (more)

Subjects/Keywords: antimônio; antimony; leishmaniasis; leishmaniose; liposome; lipossoma

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APA (6th Edition):

Borborema, S. E. T. (2010). Desenvolvimento e farmacocinética de antimônio encapsulado em lipossomas de fosfatidilserina utilizando radioisótopos em leishmaniose experimental. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/85/85131/tde-29082011-131053/ ;

Chicago Manual of Style (16th Edition):

Borborema, Samanta Etel Treiger. “Desenvolvimento e farmacocinética de antimônio encapsulado em lipossomas de fosfatidilserina utilizando radioisótopos em leishmaniose experimental.” 2010. Doctoral Dissertation, University of São Paulo. Accessed June 20, 2019. http://www.teses.usp.br/teses/disponiveis/85/85131/tde-29082011-131053/ ;.

MLA Handbook (7th Edition):

Borborema, Samanta Etel Treiger. “Desenvolvimento e farmacocinética de antimônio encapsulado em lipossomas de fosfatidilserina utilizando radioisótopos em leishmaniose experimental.” 2010. Web. 20 Jun 2019.

Vancouver:

Borborema SET. Desenvolvimento e farmacocinética de antimônio encapsulado em lipossomas de fosfatidilserina utilizando radioisótopos em leishmaniose experimental. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2019 Jun 20]. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-29082011-131053/ ;.

Council of Science Editors:

Borborema SET. Desenvolvimento e farmacocinética de antimônio encapsulado em lipossomas de fosfatidilserina utilizando radioisótopos em leishmaniose experimental. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/85/85131/tde-29082011-131053/ ;

11. Shetty, Raghavendra. Liposome formulation of anticancer drug and its pharmacokinetics and toxicokinetic evaluation.

Degree: 2010, Nirma University

The aim of the present study was to design a controlled delivery system of Irinotecan using PEGylated liposomes to overcome the limitations of conventional i.v.… (more)

Subjects/Keywords: Pharmacy; Liposome; Pharmacokinetics; Toxicokinetic; Anticancer drug

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APA (6th Edition):

Shetty, R. (2010). Liposome formulation of anticancer drug and its pharmacokinetics and toxicokinetic evaluation. (Thesis). Nirma University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/2315

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):

Shetty, Raghavendra. “Liposome formulation of anticancer drug and its pharmacokinetics and toxicokinetic evaluation.” 2010. Thesis, Nirma University. Accessed June 20, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/2315.

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

MLA Handbook (7th Edition):

Shetty, Raghavendra. “Liposome formulation of anticancer drug and its pharmacokinetics and toxicokinetic evaluation.” 2010. Web. 20 Jun 2019.

Vancouver:

Shetty R. Liposome formulation of anticancer drug and its pharmacokinetics and toxicokinetic evaluation. [Internet] [Thesis]. Nirma University; 2010. [cited 2019 Jun 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2315.

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

Council of Science Editors:

Shetty R. Liposome formulation of anticancer drug and its pharmacokinetics and toxicokinetic evaluation. [Thesis]. Nirma University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/2315

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


NSYSU

12. Yang, Hsin-yi. Bovine serum albumin with glycated carboxyl groups shows a novel membrane-damaging activity.

Degree: Master, Institute of Biomedical Sciences, 2013, NSYSU

 The aim of the present study is to investigate the effect of glycation on structur and functional properties of bovine serum albumin (BSA). Glucose and… (more)

Subjects/Keywords: glycation; liposome; membrane fusion; membrane-damaging activities

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APA (6th Edition):

Yang, H. (2013). Bovine serum albumin with glycated carboxyl groups shows a novel membrane-damaging activity. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622113-093117

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):

Yang, Hsin-yi. “Bovine serum albumin with glycated carboxyl groups shows a novel membrane-damaging activity.” 2013. Thesis, NSYSU. Accessed June 20, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622113-093117.

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

MLA Handbook (7th Edition):

Yang, Hsin-yi. “Bovine serum albumin with glycated carboxyl groups shows a novel membrane-damaging activity.” 2013. Web. 20 Jun 2019.

Vancouver:

Yang H. Bovine serum albumin with glycated carboxyl groups shows a novel membrane-damaging activity. [Internet] [Thesis]. NSYSU; 2013. [cited 2019 Jun 20]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622113-093117.

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

Council of Science Editors:

Yang H. Bovine serum albumin with glycated carboxyl groups shows a novel membrane-damaging activity. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0622113-093117

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


Penn State University

13. Wiley, Nicholas J. Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model.

Degree: MS, Neuroscience, 2008, Penn State University

 Amyotrophic lateral sclerosis (ALS) is a rapidly progressive and fatal neurological disease characterized by the selective death of motor neurons. There is substantial evidence that… (more)

Subjects/Keywords: amyotrophic lateral sclerosis; SOD1; liposome; minocycline; microglia

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APA (6th Edition):

Wiley, N. J. (2008). Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8464

Chicago Manual of Style (16th Edition):

Wiley, Nicholas J. “Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model.” 2008. Masters Thesis, Penn State University. Accessed June 20, 2019. https://etda.libraries.psu.edu/catalog/8464.

MLA Handbook (7th Edition):

Wiley, Nicholas J. “Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model.” 2008. Web. 20 Jun 2019.

Vancouver:

Wiley NJ. Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model. [Internet] [Masters thesis]. Penn State University; 2008. [cited 2019 Jun 20]. Available from: https://etda.libraries.psu.edu/catalog/8464.

Council of Science Editors:

Wiley NJ. Targeted Liposomes for Treatment of ALS in Mutant SOD1-G93A Mouse Model. [Masters Thesis]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8464


Penn State University

14. Skibinski, Christine G. preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention.

Degree: PhD, Biochemistry and Molecular Biology, 2015, Penn State University

 As discussed in Chapter 1, Breast cancer is the second leading cause of cancer death in women in the United States, with about 2 million… (more)

Subjects/Keywords: Docosahexaenoic Acid; Liposome; Breast Cancer Prevention

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APA (6th Edition):

Skibinski, C. G. (2015). preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/26720

Chicago Manual of Style (16th Edition):

Skibinski, Christine G. “preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention.” 2015. Doctoral Dissertation, Penn State University. Accessed June 20, 2019. https://etda.libraries.psu.edu/catalog/26720.

MLA Handbook (7th Edition):

Skibinski, Christine G. “preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention.” 2015. Web. 20 Jun 2019.

Vancouver:

Skibinski CG. preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention. [Internet] [Doctoral dissertation]. Penn State University; 2015. [cited 2019 Jun 20]. Available from: https://etda.libraries.psu.edu/catalog/26720.

Council of Science Editors:

Skibinski CG. preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention. [Doctoral Dissertation]. Penn State University; 2015. Available from: https://etda.libraries.psu.edu/catalog/26720


University of Toronto

15. Huang. Comparison of CT and Optical Image-based Assessment of Liposome Distribution.

Degree: 2012, University of Toronto

The use of multimodal imaging as a tool to assess the in vivo pharmacokinetics and biodistribution of nanoparticles is important in drug development and imaging-guided… (more)

Subjects/Keywords: liposome; contrast agents; CT; optical; FMT; 0572

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APA (6th Edition):

Huang. (2012). Comparison of CT and Optical Image-based Assessment of Liposome Distribution. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/35551

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Huang. “Comparison of CT and Optical Image-based Assessment of Liposome Distribution.” 2012. Masters Thesis, University of Toronto. Accessed June 20, 2019. http://hdl.handle.net/1807/35551.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Huang. “Comparison of CT and Optical Image-based Assessment of Liposome Distribution.” 2012. Web. 20 Jun 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Huang. Comparison of CT and Optical Image-based Assessment of Liposome Distribution. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Jun 20]. Available from: http://hdl.handle.net/1807/35551.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Huang. Comparison of CT and Optical Image-based Assessment of Liposome Distribution. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/35551

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

16. Garnier, Boris. Développement de vecteurs liposomaux fonctionnalisés par des protéines dérivées de l’Annexine 5 et encapsulant des marqueurs pour l’imagerie : Development of liposomal vectors functionalized by Annexin5 derived proteins and encapsulating imaging compounds.

Degree: Docteur es, Sciences, technologie, santé. Biochimie, 2009, Université de Bordeaux Segalen

Ce sujet se situe dans le cadre de la mise au point de systèmes de délivrance de composés thérapeutiques ou d’imagerie, c’est à dire d’objets… (more)

Subjects/Keywords: Annexine 5 (Anx5); Liposome; Fonctionnalisation; Magnétoliposome; Encapsulation

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APA (6th Edition):

Garnier, B. (2009). Développement de vecteurs liposomaux fonctionnalisés par des protéines dérivées de l’Annexine 5 et encapsulant des marqueurs pour l’imagerie : Development of liposomal vectors functionalized by Annexin5 derived proteins and encapsulating imaging compounds. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2009BOR21651

Chicago Manual of Style (16th Edition):

Garnier, Boris. “Développement de vecteurs liposomaux fonctionnalisés par des protéines dérivées de l’Annexine 5 et encapsulant des marqueurs pour l’imagerie : Development of liposomal vectors functionalized by Annexin5 derived proteins and encapsulating imaging compounds.” 2009. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed June 20, 2019. http://www.theses.fr/2009BOR21651.

MLA Handbook (7th Edition):

Garnier, Boris. “Développement de vecteurs liposomaux fonctionnalisés par des protéines dérivées de l’Annexine 5 et encapsulant des marqueurs pour l’imagerie : Development of liposomal vectors functionalized by Annexin5 derived proteins and encapsulating imaging compounds.” 2009. Web. 20 Jun 2019.

Vancouver:

Garnier B. Développement de vecteurs liposomaux fonctionnalisés par des protéines dérivées de l’Annexine 5 et encapsulant des marqueurs pour l’imagerie : Development of liposomal vectors functionalized by Annexin5 derived proteins and encapsulating imaging compounds. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2009. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2009BOR21651.

Council of Science Editors:

Garnier B. Développement de vecteurs liposomaux fonctionnalisés par des protéines dérivées de l’Annexine 5 et encapsulant des marqueurs pour l’imagerie : Development of liposomal vectors functionalized by Annexin5 derived proteins and encapsulating imaging compounds. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2009. Available from: http://www.theses.fr/2009BOR21651


University of Minnesota

17. Atchison, Nicole Ann. Nanomaterial solutions for the protection of insulin producing beta cells.

Degree: PhD, Biomedical Engineering, 2013, University of Minnesota

 Islet transplantation is a promising treatment for type 1 diabetes. However, even with the many successes, islet transplantation has yet to reach its full potential.… (more)

Subjects/Keywords: ATP; Beta cells; Liposome; Nanomaterials; Peptides

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APA (6th Edition):

Atchison, N. A. (2013). Nanomaterial solutions for the protection of insulin producing beta cells. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/161507

Chicago Manual of Style (16th Edition):

Atchison, Nicole Ann. “Nanomaterial solutions for the protection of insulin producing beta cells.” 2013. Doctoral Dissertation, University of Minnesota. Accessed June 20, 2019. http://purl.umn.edu/161507.

MLA Handbook (7th Edition):

Atchison, Nicole Ann. “Nanomaterial solutions for the protection of insulin producing beta cells.” 2013. Web. 20 Jun 2019.

Vancouver:

Atchison NA. Nanomaterial solutions for the protection of insulin producing beta cells. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2019 Jun 20]. Available from: http://purl.umn.edu/161507.

Council of Science Editors:

Atchison NA. Nanomaterial solutions for the protection of insulin producing beta cells. [Doctoral Dissertation]. University of Minnesota; 2013. Available from: http://purl.umn.edu/161507


University of California – San Francisco

18. Dolor, Aaron. Modifications of the Target or Therapeutic for Improved Drug Delivery.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2018, University of California – San Francisco

 Liposomes featuring a lipid bilayer surrounding an aqueous core, have been utilized as carriers for drugs and macromolecules since the 1970s. Liposomal drug encapsulation improves… (more)

Subjects/Keywords: Pharmaceutical sciences; Collagenase; Drug delivery; Liposome; PEG

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APA (6th Edition):

Dolor, A. (2018). Modifications of the Target or Therapeutic for Improved Drug Delivery. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2nm111c4

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):

Dolor, Aaron. “Modifications of the Target or Therapeutic for Improved Drug Delivery.” 2018. Thesis, University of California – San Francisco. Accessed June 20, 2019. http://www.escholarship.org/uc/item/2nm111c4.

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

MLA Handbook (7th Edition):

Dolor, Aaron. “Modifications of the Target or Therapeutic for Improved Drug Delivery.” 2018. Web. 20 Jun 2019.

Vancouver:

Dolor A. Modifications of the Target or Therapeutic for Improved Drug Delivery. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Jun 20]. Available from: http://www.escholarship.org/uc/item/2nm111c4.

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

Council of Science Editors:

Dolor A. Modifications of the Target or Therapeutic for Improved Drug Delivery. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/2nm111c4

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


Tulane University

19. Kurtz, Samantha. Diffusion Kinetics, Ductal Targeting, and Efficacy of Transpapillary Drug Delivery for Breast Cancer Prevention.

Degree: 2019, Tulane University

[email protected]

Transpapillary drug delivery is a novel drug administration technique that integrates the non-invasive, passive aspect of transdermal drug delivery with the targeted approach of… (more)

Subjects/Keywords: transpapillary drug delivery; breast cancer prevention; liposome

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APA (6th Edition):

Kurtz, S. (2019). Diffusion Kinetics, Ductal Targeting, and Efficacy of Transpapillary Drug Delivery for Breast Cancer Prevention. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:90931

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):

Kurtz, Samantha. “Diffusion Kinetics, Ductal Targeting, and Efficacy of Transpapillary Drug Delivery for Breast Cancer Prevention.” 2019. Thesis, Tulane University. Accessed June 20, 2019. https://digitallibrary.tulane.edu/islandora/object/tulane:90931.

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

MLA Handbook (7th Edition):

Kurtz, Samantha. “Diffusion Kinetics, Ductal Targeting, and Efficacy of Transpapillary Drug Delivery for Breast Cancer Prevention.” 2019. Web. 20 Jun 2019.

Vancouver:

Kurtz S. Diffusion Kinetics, Ductal Targeting, and Efficacy of Transpapillary Drug Delivery for Breast Cancer Prevention. [Internet] [Thesis]. Tulane University; 2019. [cited 2019 Jun 20]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:90931.

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

Council of Science Editors:

Kurtz S. Diffusion Kinetics, Ductal Targeting, and Efficacy of Transpapillary Drug Delivery for Breast Cancer Prevention. [Thesis]. Tulane University; 2019. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:90931

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

20. Vincourt-Vitse, Véronique. Contribution à la formulation et à l'évaluation de liposomes d'ATP : Contribution to the formulation and the evaluation of ATP liposomes.

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

Les liposomes d’ATP incluant des ligands hépatiques pourraient contribuer à améliorer le statut énergétique du greffon hépatique. Une première phase de développement a mis en… (more)

Subjects/Keywords: ATP; Liposome; Lyophilisation; HepG2; Etomoxir; ATP; Liposome; Freeze drying; HepG2; Etomoxir; 612.015

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APA (6th Edition):

Vincourt-Vitse, V. (2012). Contribution à la formulation et à l'évaluation de liposomes d'ATP : Contribution to the formulation and the evaluation of ATP liposomes. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2012PA05P651

Chicago Manual of Style (16th Edition):

Vincourt-Vitse, Véronique. “Contribution à la formulation et à l'évaluation de liposomes d'ATP : Contribution to the formulation and the evaluation of ATP liposomes.” 2012. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed June 20, 2019. http://www.theses.fr/2012PA05P651.

MLA Handbook (7th Edition):

Vincourt-Vitse, Véronique. “Contribution à la formulation et à l'évaluation de liposomes d'ATP : Contribution to the formulation and the evaluation of ATP liposomes.” 2012. Web. 20 Jun 2019.

Vancouver:

Vincourt-Vitse V. Contribution à la formulation et à l'évaluation de liposomes d'ATP : Contribution to the formulation and the evaluation of ATP liposomes. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2012. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2012PA05P651.

Council of Science Editors:

Vincourt-Vitse V. Contribution à la formulation et à l'évaluation de liposomes d'ATP : Contribution to the formulation and the evaluation of ATP liposomes. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2012. Available from: http://www.theses.fr/2012PA05P651

21. Thebault, Caroline. Liposomes théranostiques pour le ciblage magnétique et le relargage d'un antitumoral par ultrasons focalisés, suivis par IRM multiparamétrique : Theranostic liposomes for magnetic targeting and antitumoral drug release triggered by focused ultrasounds, monitored by multiparametric MRI.

Degree: Docteur es, Chimie Moléculaire, 2017, Université Pierre et Marie Curie – Paris VI

Les systèmes théranostiques associant des propriétés thérapeutiques et des propriétés d'imagerie sont développés pour permettre le suivi de traitement in vivo. La stratégie que nous… (more)

Subjects/Keywords: Liposome; Théranostic; Irm; Ca4p; Hifu; Ciblage magnétique; Theranostic liposome; Magnetic targeting / MRI; Thermosensitive; 541.2

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APA (6th Edition):

Thebault, C. (2017). Liposomes théranostiques pour le ciblage magnétique et le relargage d'un antitumoral par ultrasons focalisés, suivis par IRM multiparamétrique : Theranostic liposomes for magnetic targeting and antitumoral drug release triggered by focused ultrasounds, monitored by multiparametric MRI. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066022

Chicago Manual of Style (16th Edition):

Thebault, Caroline. “Liposomes théranostiques pour le ciblage magnétique et le relargage d'un antitumoral par ultrasons focalisés, suivis par IRM multiparamétrique : Theranostic liposomes for magnetic targeting and antitumoral drug release triggered by focused ultrasounds, monitored by multiparametric MRI.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed June 20, 2019. http://www.theses.fr/2017PA066022.

MLA Handbook (7th Edition):

Thebault, Caroline. “Liposomes théranostiques pour le ciblage magnétique et le relargage d'un antitumoral par ultrasons focalisés, suivis par IRM multiparamétrique : Theranostic liposomes for magnetic targeting and antitumoral drug release triggered by focused ultrasounds, monitored by multiparametric MRI.” 2017. Web. 20 Jun 2019.

Vancouver:

Thebault C. Liposomes théranostiques pour le ciblage magnétique et le relargage d'un antitumoral par ultrasons focalisés, suivis par IRM multiparamétrique : Theranostic liposomes for magnetic targeting and antitumoral drug release triggered by focused ultrasounds, monitored by multiparametric MRI. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2017PA066022.

Council of Science Editors:

Thebault C. Liposomes théranostiques pour le ciblage magnétique et le relargage d'un antitumoral par ultrasons focalisés, suivis par IRM multiparamétrique : Theranostic liposomes for magnetic targeting and antitumoral drug release triggered by focused ultrasounds, monitored by multiparametric MRI. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066022

22. Massiot, Julien. Conception de nanomédicaments photostimulables à base de lipides et porphyrines ou de conjugués lipide-porphyrine pour la libération contrôlée de substances actives : Design of photoactivatable drug delivery systems made of lipids and porphyrins or lipid-porphyrin conjugates for the controlled release of active pharmaceutical ingredients.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2018, Paris Saclay

L’objectif des travaux de cette thèse était de développer un système de délivrance stimulus-sensible innovant. Basé sur des vésicules lipidiques, il permet la libération d’une… (more)

Subjects/Keywords: Lipide; Porphyrine; Conjugué; Libération; Lumière; Liposome; Lipid; Porphyrin; Conjugate; Release; Light; Liposome

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APA (6th Edition):

Massiot, J. (2018). Conception de nanomédicaments photostimulables à base de lipides et porphyrines ou de conjugués lipide-porphyrine pour la libération contrôlée de substances actives : Design of photoactivatable drug delivery systems made of lipids and porphyrins or lipid-porphyrin conjugates for the controlled release of active pharmaceutical ingredients. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS290

Chicago Manual of Style (16th Edition):

Massiot, Julien. “Conception de nanomédicaments photostimulables à base de lipides et porphyrines ou de conjugués lipide-porphyrine pour la libération contrôlée de substances actives : Design of photoactivatable drug delivery systems made of lipids and porphyrins or lipid-porphyrin conjugates for the controlled release of active pharmaceutical ingredients.” 2018. Doctoral Dissertation, Paris Saclay. Accessed June 20, 2019. http://www.theses.fr/2018SACLS290.

MLA Handbook (7th Edition):

Massiot, Julien. “Conception de nanomédicaments photostimulables à base de lipides et porphyrines ou de conjugués lipide-porphyrine pour la libération contrôlée de substances actives : Design of photoactivatable drug delivery systems made of lipids and porphyrins or lipid-porphyrin conjugates for the controlled release of active pharmaceutical ingredients.” 2018. Web. 20 Jun 2019.

Vancouver:

Massiot J. Conception de nanomédicaments photostimulables à base de lipides et porphyrines ou de conjugués lipide-porphyrine pour la libération contrôlée de substances actives : Design of photoactivatable drug delivery systems made of lipids and porphyrins or lipid-porphyrin conjugates for the controlled release of active pharmaceutical ingredients. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2018SACLS290.

Council of Science Editors:

Massiot J. Conception de nanomédicaments photostimulables à base de lipides et porphyrines ou de conjugués lipide-porphyrine pour la libération contrôlée de substances actives : Design of photoactivatable drug delivery systems made of lipids and porphyrins or lipid-porphyrin conjugates for the controlled release of active pharmaceutical ingredients. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS290

23. Sala, Mourad. Nanovecteurs lipidiques pour une application topique dans le psoriasis et sa complication arthritique : Lipid nanocarriers for topical application in psoriasis and psoriatic arthritis.

Degree: Docteur es, Pharmacotechnie, 2017, Lyon

Le psoriasis est une maladie de peau auto-immune et chronique. Le rhumatisme psoriasique est une de ses principales complications qui est très invalidante pour les… (more)

Subjects/Keywords: Vésicule lipidique; Liposome; Préparation; Diclofénac; Ciclosporine A; Encapsulation; Lipid vesicles; Liposome; Preparation; Diclofenac; Ciclosporine A; Encapsulation; 615

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APA (6th Edition):

Sala, M. (2017). Nanovecteurs lipidiques pour une application topique dans le psoriasis et sa complication arthritique : Lipid nanocarriers for topical application in psoriasis and psoriatic arthritis. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2017LYSE1193

Chicago Manual of Style (16th Edition):

Sala, Mourad. “Nanovecteurs lipidiques pour une application topique dans le psoriasis et sa complication arthritique : Lipid nanocarriers for topical application in psoriasis and psoriatic arthritis.” 2017. Doctoral Dissertation, Lyon. Accessed June 20, 2019. http://www.theses.fr/2017LYSE1193.

MLA Handbook (7th Edition):

Sala, Mourad. “Nanovecteurs lipidiques pour une application topique dans le psoriasis et sa complication arthritique : Lipid nanocarriers for topical application in psoriasis and psoriatic arthritis.” 2017. Web. 20 Jun 2019.

Vancouver:

Sala M. Nanovecteurs lipidiques pour une application topique dans le psoriasis et sa complication arthritique : Lipid nanocarriers for topical application in psoriasis and psoriatic arthritis. [Internet] [Doctoral dissertation]. Lyon; 2017. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2017LYSE1193.

Council of Science Editors:

Sala M. Nanovecteurs lipidiques pour une application topique dans le psoriasis et sa complication arthritique : Lipid nanocarriers for topical application in psoriasis and psoriatic arthritis. [Doctoral Dissertation]. Lyon; 2017. Available from: http://www.theses.fr/2017LYSE1193

24. Kakhi, Zahra. Conception de constructions liposomiques destinées à la vaccination antitumorale par voie respiratoire : Conception of liposomal constructs for antitumoral vaccination by respiratory route.

Degree: Docteur es, Chimie biologique et thérapeutique, 2014, Université de Strasbourg

Avec l’identification des antigènes tumoraux et la compréhension de la réponse immunitaire mucosale, la vaccination par voie respiratoire est devenue un champ d’investigation prometteur pour… (more)

Subjects/Keywords: Vaccin peptidique; Liposome; Nanovecteur; Formulation; Voie respiratoire; Voie nasale; Cancer; Peptide vaccine; Liposome; Nanoparticle; Formulation; Respiratory route; Nasal route; Cancer; 615.37

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APA (6th Edition):

Kakhi, Z. (2014). Conception de constructions liposomiques destinées à la vaccination antitumorale par voie respiratoire : Conception of liposomal constructs for antitumoral vaccination by respiratory route. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2014STRAF044

Chicago Manual of Style (16th Edition):

Kakhi, Zahra. “Conception de constructions liposomiques destinées à la vaccination antitumorale par voie respiratoire : Conception of liposomal constructs for antitumoral vaccination by respiratory route.” 2014. Doctoral Dissertation, Université de Strasbourg. Accessed June 20, 2019. http://www.theses.fr/2014STRAF044.

MLA Handbook (7th Edition):

Kakhi, Zahra. “Conception de constructions liposomiques destinées à la vaccination antitumorale par voie respiratoire : Conception of liposomal constructs for antitumoral vaccination by respiratory route.” 2014. Web. 20 Jun 2019.

Vancouver:

Kakhi Z. Conception de constructions liposomiques destinées à la vaccination antitumorale par voie respiratoire : Conception of liposomal constructs for antitumoral vaccination by respiratory route. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2014. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2014STRAF044.

Council of Science Editors:

Kakhi Z. Conception de constructions liposomiques destinées à la vaccination antitumorale par voie respiratoire : Conception of liposomal constructs for antitumoral vaccination by respiratory route. [Doctoral Dissertation]. Université de Strasbourg; 2014. Available from: http://www.theses.fr/2014STRAF044


Université de Bordeaux I

25. Wan, Yali. Développement de nanovecteurs polymériques et lipidiques fonctionnalisés par des anticorps pour cibler des cellules cancéreuses : Development of antibody functionalized polymeric and lipidic nanoparticles for targeting cancer cells.

Degree: Docteur es, Biochimie, 2012, Université de Bordeaux I

Ce travail, qui fait partie d’un projet européen, « NANOTHER », est focalisé sur la fonctionnalisation de nanoparticules polymériques et lipidiques fonctionnalisées par des anticorps Herceptine® pour… (more)

Subjects/Keywords: Polymersome; Liposome; Anx5-ZZ; Herceptine®; Fonctionnalisation; Cellules HER2+; Polymersome; Liposome; Anx5-ZZ; Herceptin®; Functionalization; HER2+ cells

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APA (6th Edition):

Wan, Y. (2012). Développement de nanovecteurs polymériques et lipidiques fonctionnalisés par des anticorps pour cibler des cellules cancéreuses : Development of antibody functionalized polymeric and lipidic nanoparticles for targeting cancer cells. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2012BOR14736

Chicago Manual of Style (16th Edition):

Wan, Yali. “Développement de nanovecteurs polymériques et lipidiques fonctionnalisés par des anticorps pour cibler des cellules cancéreuses : Development of antibody functionalized polymeric and lipidic nanoparticles for targeting cancer cells.” 2012. Doctoral Dissertation, Université de Bordeaux I. Accessed June 20, 2019. http://www.theses.fr/2012BOR14736.

MLA Handbook (7th Edition):

Wan, Yali. “Développement de nanovecteurs polymériques et lipidiques fonctionnalisés par des anticorps pour cibler des cellules cancéreuses : Development of antibody functionalized polymeric and lipidic nanoparticles for targeting cancer cells.” 2012. Web. 20 Jun 2019.

Vancouver:

Wan Y. Développement de nanovecteurs polymériques et lipidiques fonctionnalisés par des anticorps pour cibler des cellules cancéreuses : Development of antibody functionalized polymeric and lipidic nanoparticles for targeting cancer cells. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2012. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2012BOR14736.

Council of Science Editors:

Wan Y. Développement de nanovecteurs polymériques et lipidiques fonctionnalisés par des anticorps pour cibler des cellules cancéreuses : Development of antibody functionalized polymeric and lipidic nanoparticles for targeting cancer cells. [Doctoral Dissertation]. Université de Bordeaux I; 2012. Available from: http://www.theses.fr/2012BOR14736

26. Saliba, Hanadi. Development of innovative liposome-based constructs for non-invasive cancer immunotherapy in humans : Développement de constructions liposomiques innovantes pour l’immunothérapie humaine.

Degree: Docteur es, Immunologie, 2017, Université de Strasbourg

La voie d’administration d’un vaccin et le modèle préclinique dans le lequel il est évalué sont des facteurs majeurs qui contribuent à son succès chez… (more)

Subjects/Keywords: Vaccin antitumoral; Liposome; Voie transcutanée; Souris humanisée; Tumor-specific vaccine; Liposome; Transcutaneous route; Humanized mouse; 571.96; 615.7; 616.99

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APA (6th Edition):

Saliba, H. (2017). Development of innovative liposome-based constructs for non-invasive cancer immunotherapy in humans : Développement de constructions liposomiques innovantes pour l’immunothérapie humaine. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAJ070

Chicago Manual of Style (16th Edition):

Saliba, Hanadi. “Development of innovative liposome-based constructs for non-invasive cancer immunotherapy in humans : Développement de constructions liposomiques innovantes pour l’immunothérapie humaine.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed June 20, 2019. http://www.theses.fr/2017STRAJ070.

MLA Handbook (7th Edition):

Saliba, Hanadi. “Development of innovative liposome-based constructs for non-invasive cancer immunotherapy in humans : Développement de constructions liposomiques innovantes pour l’immunothérapie humaine.” 2017. Web. 20 Jun 2019.

Vancouver:

Saliba H. Development of innovative liposome-based constructs for non-invasive cancer immunotherapy in humans : Développement de constructions liposomiques innovantes pour l’immunothérapie humaine. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2017STRAJ070.

Council of Science Editors:

Saliba H. Development of innovative liposome-based constructs for non-invasive cancer immunotherapy in humans : Développement de constructions liposomiques innovantes pour l’immunothérapie humaine. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAJ070

27. El kechai, Naila. Gels d'acide hyaluronique contenant des liposomes pour la libération prolongée d'un corticoïde dans l'oreille interne : Hyaluronic acid liposomal gels for the sustained delivery of a corticoid to the inner ear.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2015, Paris Saclay

Les traitements des pathologies de l’oreille interne par voie locale se développent en alternative aux traitements par voie générale peu efficaces et responsables de nombreux… (more)

Subjects/Keywords: Acide hyaluronique; Liposome; Oreille interne; Dexamethasone phosphate; Administration locale; Gel; Hyaluronic acid; Liposome; Inner ear; Gel; Local drug delivery; Dexamethasone phosphate

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

APA (6th Edition):

El kechai, N. (2015). Gels d'acide hyaluronique contenant des liposomes pour la libération prolongée d'un corticoïde dans l'oreille interne : Hyaluronic acid liposomal gels for the sustained delivery of a corticoid to the inner ear. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2015SACLS155

Chicago Manual of Style (16th Edition):

El kechai, Naila. “Gels d'acide hyaluronique contenant des liposomes pour la libération prolongée d'un corticoïde dans l'oreille interne : Hyaluronic acid liposomal gels for the sustained delivery of a corticoid to the inner ear.” 2015. Doctoral Dissertation, Paris Saclay. Accessed June 20, 2019. http://www.theses.fr/2015SACLS155.

MLA Handbook (7th Edition):

El kechai, Naila. “Gels d'acide hyaluronique contenant des liposomes pour la libération prolongée d'un corticoïde dans l'oreille interne : Hyaluronic acid liposomal gels for the sustained delivery of a corticoid to the inner ear.” 2015. Web. 20 Jun 2019.

Vancouver:

El kechai N. Gels d'acide hyaluronique contenant des liposomes pour la libération prolongée d'un corticoïde dans l'oreille interne : Hyaluronic acid liposomal gels for the sustained delivery of a corticoid to the inner ear. [Internet] [Doctoral dissertation]. Paris Saclay; 2015. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2015SACLS155.

Council of Science Editors:

El kechai N. Gels d'acide hyaluronique contenant des liposomes pour la libération prolongée d'un corticoïde dans l'oreille interne : Hyaluronic acid liposomal gels for the sustained delivery of a corticoid to the inner ear. [Doctoral Dissertation]. Paris Saclay; 2015. Available from: http://www.theses.fr/2015SACLS155

28. Wu, Xiao. Approche physico-chimique de la formulation de bêta-lapachone complexée ou non à des cyclodextrines, dans des préparations liposomales : Physico-chemical approach to the formulation of beta-lapachone, and its complexes with cyclodextrins, in liposomes.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2018, Paris Saclay

La bêta-lapachone (b-lap) est une substance active présentant des activités trypanocides, anti-infectieuses et anticancéreuses, avec une sélectivité thérapeutique. Cependant, en raison de sa faible hydrosolubilité… (more)

Subjects/Keywords: Beta-Lapachone; Thérapie anticancéreuse; Cyclodextrine; Liposome; Méthodes physicochimiques; Cytotoxicité; Beta-Lapachone; Anticancer therapy; Cyclodextrin; Liposome; Physico-Chemical Methods; Cytotoxicity

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

APA (6th Edition):

Wu, X. (2018). Approche physico-chimique de la formulation de bêta-lapachone complexée ou non à des cyclodextrines, dans des préparations liposomales : Physico-chemical approach to the formulation of beta-lapachone, and its complexes with cyclodextrins, in liposomes. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2018SACLS348

Chicago Manual of Style (16th Edition):

Wu, Xiao. “Approche physico-chimique de la formulation de bêta-lapachone complexée ou non à des cyclodextrines, dans des préparations liposomales : Physico-chemical approach to the formulation of beta-lapachone, and its complexes with cyclodextrins, in liposomes.” 2018. Doctoral Dissertation, Paris Saclay. Accessed June 20, 2019. http://www.theses.fr/2018SACLS348.

MLA Handbook (7th Edition):

Wu, Xiao. “Approche physico-chimique de la formulation de bêta-lapachone complexée ou non à des cyclodextrines, dans des préparations liposomales : Physico-chemical approach to the formulation of beta-lapachone, and its complexes with cyclodextrins, in liposomes.” 2018. Web. 20 Jun 2019.

Vancouver:

Wu X. Approche physico-chimique de la formulation de bêta-lapachone complexée ou non à des cyclodextrines, dans des préparations liposomales : Physico-chemical approach to the formulation of beta-lapachone, and its complexes with cyclodextrins, in liposomes. [Internet] [Doctoral dissertation]. Paris Saclay; 2018. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2018SACLS348.

Council of Science Editors:

Wu X. Approche physico-chimique de la formulation de bêta-lapachone complexée ou non à des cyclodextrines, dans des préparations liposomales : Physico-chemical approach to the formulation of beta-lapachone, and its complexes with cyclodextrins, in liposomes. [Doctoral Dissertation]. Paris Saclay; 2018. Available from: http://www.theses.fr/2018SACLS348

29. Karim, Reatul. Design of Nanocarriers to Deliver Small Hydrophobic Molecules for Glioblastoma Treatment : Développement des nanoparticules pour la délivrance de molécules hydrophobes de faible poids moléculaire dans le contexte du traitement du glioblastome.

Degree: Docteur es, Pharmacie, 2017, Angers; Université de Liège. Faculté de médecine

Le but de cette thèse de doctorat fut de développer des nanoparticules pour la délivrance de deux molécules hydrophobes de faible poids moléculaire, l’apigénine (AG)… (more)

Subjects/Keywords: Nanoparticule; Nanocapsule lipidique; Liposome; Peptide pénétrant; Apigénine; Ferrocifène; Nanocarrier; Lipid nanocapsule; Liposome; Glioblastoma; Cell-Penetrating peptide; Apigenin; Ferrocifen; 615.6

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

APA (6th Edition):

Karim, R. (2017). Design of Nanocarriers to Deliver Small Hydrophobic Molecules for Glioblastoma Treatment : Développement des nanoparticules pour la délivrance de molécules hydrophobes de faible poids moléculaire dans le contexte du traitement du glioblastome. (Doctoral Dissertation). Angers; Université de Liège. Faculté de médecine. Retrieved from http://www.theses.fr/2017ANGE0055

Chicago Manual of Style (16th Edition):

Karim, Reatul. “Design of Nanocarriers to Deliver Small Hydrophobic Molecules for Glioblastoma Treatment : Développement des nanoparticules pour la délivrance de molécules hydrophobes de faible poids moléculaire dans le contexte du traitement du glioblastome.” 2017. Doctoral Dissertation, Angers; Université de Liège. Faculté de médecine. Accessed June 20, 2019. http://www.theses.fr/2017ANGE0055.

MLA Handbook (7th Edition):

Karim, Reatul. “Design of Nanocarriers to Deliver Small Hydrophobic Molecules for Glioblastoma Treatment : Développement des nanoparticules pour la délivrance de molécules hydrophobes de faible poids moléculaire dans le contexte du traitement du glioblastome.” 2017. Web. 20 Jun 2019.

Vancouver:

Karim R. Design of Nanocarriers to Deliver Small Hydrophobic Molecules for Glioblastoma Treatment : Développement des nanoparticules pour la délivrance de molécules hydrophobes de faible poids moléculaire dans le contexte du traitement du glioblastome. [Internet] [Doctoral dissertation]. Angers; Université de Liège. Faculté de médecine; 2017. [cited 2019 Jun 20]. Available from: http://www.theses.fr/2017ANGE0055.

Council of Science Editors:

Karim R. Design of Nanocarriers to Deliver Small Hydrophobic Molecules for Glioblastoma Treatment : Développement des nanoparticules pour la délivrance de molécules hydrophobes de faible poids moléculaire dans le contexte du traitement du glioblastome. [Doctoral Dissertation]. Angers; Université de Liège. Faculté de médecine; 2017. Available from: http://www.theses.fr/2017ANGE0055

30. Nakhuru, K S. Carcinogenesis response modulation by gelonin encapsulated in liposome; -.

Degree: Biochemistry, 2006, North-Eastern Hill University

Abstract not available newline

Bibliography p. 112-125

Advisors/Committee Members: Alam, Anis.

Subjects/Keywords: Carcinogenesis; Modulation; Gelonin Encapsulated; Liposome

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

APA (6th Edition):

Nakhuru, K. S. (2006). Carcinogenesis response modulation by gelonin encapsulated in liposome; -. (Thesis). North-Eastern Hill University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/54873

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):

Nakhuru, K S. “Carcinogenesis response modulation by gelonin encapsulated in liposome; -.” 2006. Thesis, North-Eastern Hill University. Accessed June 20, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/54873.

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

MLA Handbook (7th Edition):

Nakhuru, K S. “Carcinogenesis response modulation by gelonin encapsulated in liposome; -.” 2006. Web. 20 Jun 2019.

Vancouver:

Nakhuru KS. Carcinogenesis response modulation by gelonin encapsulated in liposome; -. [Internet] [Thesis]. North-Eastern Hill University; 2006. [cited 2019 Jun 20]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54873.

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

Council of Science Editors:

Nakhuru KS. Carcinogenesis response modulation by gelonin encapsulated in liposome; -. [Thesis]. North-Eastern Hill University; 2006. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/54873

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

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