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You searched for subject:(liposome). Showing records 1 – 30 of 245 total matches.

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California State Polytechnic University – Pomona

1. Faneuff, Eden. CMI Liposomes with Pam3CAG Adjuvant and No Influenza Proteins Protect Mice from Influenza Infection.

Degree: MS, Department of Biological Sciences, 2020, California State Polytechnic University – Pomona

 Introduction: Influenza virus can cause epidemic or pandemic infections due to the emergence of new viral strains to which the host has little or no… (more)

Subjects/Keywords: liposome

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APA (6th Edition):

Faneuff, E. (2020). CMI Liposomes with Pam3CAG Adjuvant and No Influenza Proteins Protect Mice from Influenza Infection. (Masters Thesis). California State Polytechnic University – Pomona. Retrieved from http://hdl.handle.net/10211.3/214801

Chicago Manual of Style (16th Edition):

Faneuff, Eden. “CMI Liposomes with Pam3CAG Adjuvant and No Influenza Proteins Protect Mice from Influenza Infection.” 2020. Masters Thesis, California State Polytechnic University – Pomona. Accessed November 26, 2020. http://hdl.handle.net/10211.3/214801.

MLA Handbook (7th Edition):

Faneuff, Eden. “CMI Liposomes with Pam3CAG Adjuvant and No Influenza Proteins Protect Mice from Influenza Infection.” 2020. Web. 26 Nov 2020.

Vancouver:

Faneuff E. CMI Liposomes with Pam3CAG Adjuvant and No Influenza Proteins Protect Mice from Influenza Infection. [Internet] [Masters thesis]. California State Polytechnic University – Pomona; 2020. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10211.3/214801.

Council of Science Editors:

Faneuff E. CMI Liposomes with Pam3CAG Adjuvant and No Influenza Proteins Protect Mice from Influenza Infection. [Masters Thesis]. California State Polytechnic University – Pomona; 2020. Available from: http://hdl.handle.net/10211.3/214801


Dalhousie University

2. 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 November 26, 2020. http://hdl.handle.net/10222/54045.

MLA Handbook (7th Edition):

Li, Zhiyu. “ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES.” 2014. Web. 26 Nov 2020.

Vancouver:

Li Z. ENCAPSULATION OF BIOACTIVE SALMON PROTEIN HYDROLYSATES WITH CHITOSAN-COATED LIPOSOMES. [Internet] [Masters thesis]. Dalhousie University; 2014. [cited 2020 Nov 26]. 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

3. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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


Cornell University

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

Degree: PhD, Food Science and Technology, 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. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/41168

Chicago Manual of Style (16th Edition):

Tsai, Wen-Chyan. “Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process.” 2015. Doctoral Dissertation, Cornell University. Accessed November 26, 2020. http://hdl.handle.net/1813/41168.

MLA Handbook (7th Edition):

Tsai, Wen-Chyan. “Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process.” 2015. Web. 26 Nov 2020.

Vancouver:

Tsai W. Characterization And Applications Of Liposomes Microencapsulated By A Novel Supercritical Fluid Process. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1813/41168.

Council of Science Editors:

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


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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Rutherford H. Structural investigations of liposomes: effect of phospholipid hydrocarbon length and incorporation of sphingomyelin. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Nov 26]. 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


Penn State University

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

Degree: 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. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15235

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):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Thesis, Penn State University. Accessed November 26, 2020. https://submit-etda.libraries.psu.edu/catalog/15235.

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

MLA Handbook (7th Edition):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Web. 26 Nov 2020.

Vancouver:

Sutermaster BA. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. [Internet] [Thesis]. Penn State University; 2012. [cited 2020 Nov 26]. Available from: https://submit-etda.libraries.psu.edu/catalog/15235.

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

Council of Science Editors:

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

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


University of California – San Francisco

7. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Perttu E. The Effect of Lipid Chemistry and Structure on Liposome Formation. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2020 Nov 26]. 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


University of Notre Dame

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

Degree: 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>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/pc289g5791g

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):

Froude, Victoria Elizabeth. “AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>.” 2011. Thesis, University of Notre Dame. Accessed November 26, 2020. https://curate.nd.edu/show/pc289g5791g.

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

MLA Handbook (7th Edition):

Froude, Victoria Elizabeth. “AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>.” 2011. Web. 26 Nov 2020.

Vancouver:

Froude VE. AC-Electrokinetic Formation, Manipulation, and Induced Release of Lipid and Surfactant Based Vesicles</h1>. [Internet] [Thesis]. University of Notre Dame; 2011. [cited 2020 Nov 26]. Available from: https://curate.nd.edu/show/pc289g5791g.

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

Council of Science Editors:

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

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


Louisiana State University

9. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Chanda D. Liposomal uptake of silver and gold nanoparticles. [Internet] [Masters thesis]. Louisiana State University; 2013. [cited 2020 Nov 26]. 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

10. 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, Université Paris-Saclay (ComUE)

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). Université Paris-Saclay (ComUE). 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, Université Paris-Saclay (ComUE). Accessed November 26, 2020. 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. 26 Nov 2020.

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]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Nov 26]. 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]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS031


NSYSU

11. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Yang H. Bovine serum albumin with glycated carboxyl groups shows a novel membrane-damaging activity. [Internet] [Thesis]. NSYSU; 2013. [cited 2020 Nov 26]. 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


Tulane University

12. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Kurtz S. Diffusion Kinetics, Ductal Targeting, and Efficacy of Transpapillary Drug Delivery for Breast Cancer Prevention. [Internet] [Thesis]. Tulane University; 2019. [cited 2020 Nov 26]. 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

13. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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/ ;

14. Michelon, Mariano, 1986-. Production of Liposomal Systems by Microfluidic Devices aiming Food Applications : Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias: Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias.

Degree: 2017, Universidade Estadual de Campinas

 Abstract: The project evaluated the technological development of microfluidic processes for production of liposomal structures aiming their use as delivery systems for food industries. In… (more)

Subjects/Keywords: Lipossomas; Microfluidica; Lecitina; Liposome; Microfluidics; Lecithin

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

APA (6th Edition):

Michelon, Mariano, 1. (2017). Production of Liposomal Systems by Microfluidic Devices aiming Food Applications : Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias: Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias. (Thesis). Universidade Estadual de Campinas. Retrieved from http://repositorio.unicamp.br/jspui/handle/REPOSIP/322495

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):

Michelon, Mariano, 1986-. “Production of Liposomal Systems by Microfluidic Devices aiming Food Applications : Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias: Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias.” 2017. Thesis, Universidade Estadual de Campinas. Accessed November 26, 2020. http://repositorio.unicamp.br/jspui/handle/REPOSIP/322495.

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

MLA Handbook (7th Edition):

Michelon, Mariano, 1986-. “Production of Liposomal Systems by Microfluidic Devices aiming Food Applications : Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias: Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias.” 2017. Web. 26 Nov 2020.

Vancouver:

Michelon, Mariano 1. Production of Liposomal Systems by Microfluidic Devices aiming Food Applications : Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias: Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias. [Internet] [Thesis]. Universidade Estadual de Campinas; 2017. [cited 2020 Nov 26]. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/322495.

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

Council of Science Editors:

Michelon, Mariano 1. Production of Liposomal Systems by Microfluidic Devices aiming Food Applications : Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias: Produção de sistemas lipossomais em dispositivos microfluídicos visando aplicações alimentícias. [Thesis]. Universidade Estadual de Campinas; 2017. Available from: http://repositorio.unicamp.br/jspui/handle/REPOSIP/322495

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

15. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Shetty R. Liposome formulation of anticancer drug and its pharmacokinetics and toxicokinetic evaluation. [Internet] [Thesis]. Nirma University; 2010. [cited 2020 Nov 26]. 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


Penn State University

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

Degree: 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. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/26720

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):

Skibinski, Christine G. “preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention.” 2015. Thesis, Penn State University. Accessed November 26, 2020. https://submit-etda.libraries.psu.edu/catalog/26720.

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

MLA Handbook (7th Edition):

Skibinski, Christine G. “preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention.” 2015. Web. 26 Nov 2020.

Vancouver:

Skibinski CG. preclinical investigations into the role of omega-3 fatty acids for breast cancer prevention. [Internet] [Thesis]. Penn State University; 2015. [cited 2020 Nov 26]. Available from: https://submit-etda.libraries.psu.edu/catalog/26720.

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

Council of Science Editors:

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

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


University of Toronto

17. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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


Northeastern University

18. Shi, Di. Multi-functionalized Liposome For Brain Drug Delivery To Treat Glioblastoma.

Degree: PhD, Department of Chemical Engineering, 2018, Northeastern University

 To date, delivery of therapeutic agents into the brain to target malignant brain tumors such as glioblastoma multiforme (GBM) remains a significant challenge due to… (more)

Subjects/Keywords: drug delivery; glioblastoma; liposome; nanomedicine; Chemical engineering

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

APA (6th Edition):

Shi, D. (2018). Multi-functionalized Liposome For Brain Drug Delivery To Treat Glioblastoma. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20316322

Chicago Manual of Style (16th Edition):

Shi, Di. “Multi-functionalized Liposome For Brain Drug Delivery To Treat Glioblastoma.” 2018. Doctoral Dissertation, Northeastern University. Accessed November 26, 2020. http://hdl.handle.net/2047/D20316322.

MLA Handbook (7th Edition):

Shi, Di. “Multi-functionalized Liposome For Brain Drug Delivery To Treat Glioblastoma.” 2018. Web. 26 Nov 2020.

Vancouver:

Shi D. Multi-functionalized Liposome For Brain Drug Delivery To Treat Glioblastoma. [Internet] [Doctoral dissertation]. Northeastern University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/2047/D20316322.

Council of Science Editors:

Shi D. Multi-functionalized Liposome For Brain Drug Delivery To Treat Glioblastoma. [Doctoral Dissertation]. Northeastern University; 2018. Available from: http://hdl.handle.net/2047/D20316322


University of Minnesota

19. 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 November 26, 2020. http://purl.umn.edu/161507.

MLA Handbook (7th Edition):

Atchison, Nicole Ann. “Nanomaterial solutions for the protection of insulin producing beta cells.” 2013. Web. 26 Nov 2020.

Vancouver:

Atchison NA. Nanomaterial solutions for the protection of insulin producing beta cells. [Internet] [Doctoral dissertation]. University of Minnesota; 2013. [cited 2020 Nov 26]. 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 Georgia

20. Li, Yanhong. Towards fully synthetic anticancer vaccines.

Degree: 2014, University of Georgia

 Cancer is a menacing, worldwide health problem for which there exist no effective therapies. In this thesis, an approach towards the development of novel fully… (more)

Subjects/Keywords: cancer; vaccine; carbohydrate; Lewis antigen; liposome.

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APA (6th Edition):

Li, Y. (2014). Towards fully synthetic anticancer vaccines. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/21565

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):

Li, Yanhong. “Towards fully synthetic anticancer vaccines.” 2014. Thesis, University of Georgia. Accessed November 26, 2020. http://hdl.handle.net/10724/21565.

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

MLA Handbook (7th Edition):

Li, Yanhong. “Towards fully synthetic anticancer vaccines.” 2014. Web. 26 Nov 2020.

Vancouver:

Li Y. Towards fully synthetic anticancer vaccines. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10724/21565.

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

Council of Science Editors:

Li Y. Towards fully synthetic anticancer vaccines. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/21565

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

21. 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, Université Paris-Saclay (ComUE)

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

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). Université Paris-Saclay (ComUE). 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, Université Paris-Saclay (ComUE). Accessed November 26, 2020. 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. 26 Nov 2020.

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]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Nov 26]. 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]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS290

22. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

23. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

24. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

25. 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, Université Paris-Saclay (ComUE)

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 (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). Université Paris-Saclay (ComUE). 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, Université Paris-Saclay (ComUE). Accessed November 26, 2020. 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. 26 Nov 2020.

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]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Nov 26]. 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]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS348

26. Wang, Zhiqiang. Innovative liposomes with double encapsulation properties for the treatment of acute myeloid leukemia : Mise au point des liposomes innovants avec double encapsulation des principes actifs pour le traitement des leucémies myéloïdes aigües.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2019, Université Paris-Saclay (ComUE)

 Les leucémies sont une famille de cancers issus de la prolifération maligne des cellules hématopoïétiques. La leucémie myéloïde aigüe (AML) représente 30% des leucémies chez… (more)

Subjects/Keywords: Leucémie myelôide aigüe; Liposome; Cyclodextrine; Chlorpromazine; Vectorisation; Libération contrôlée; Acute myeloid leukemia; Liposome; Cyclodextrin; Chlorpromazine; Drug delivery; Controlled release

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

APA (6th Edition):

Wang, Z. (2019). Innovative liposomes with double encapsulation properties for the treatment of acute myeloid leukemia : Mise au point des liposomes innovants avec double encapsulation des principes actifs pour le traitement des leucémies myéloïdes aigües. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS432

Chicago Manual of Style (16th Edition):

Wang, Zhiqiang. “Innovative liposomes with double encapsulation properties for the treatment of acute myeloid leukemia : Mise au point des liposomes innovants avec double encapsulation des principes actifs pour le traitement des leucémies myéloïdes aigües.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed November 26, 2020. http://www.theses.fr/2019SACLS432.

MLA Handbook (7th Edition):

Wang, Zhiqiang. “Innovative liposomes with double encapsulation properties for the treatment of acute myeloid leukemia : Mise au point des liposomes innovants avec double encapsulation des principes actifs pour le traitement des leucémies myéloïdes aigües.” 2019. Web. 26 Nov 2020.

Vancouver:

Wang Z. Innovative liposomes with double encapsulation properties for the treatment of acute myeloid leukemia : Mise au point des liposomes innovants avec double encapsulation des principes actifs pour le traitement des leucémies myéloïdes aigües. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Nov 26]. Available from: http://www.theses.fr/2019SACLS432.

Council of Science Editors:

Wang Z. Innovative liposomes with double encapsulation properties for the treatment of acute myeloid leukemia : Mise au point des liposomes innovants avec double encapsulation des principes actifs pour le traitement des leucémies myéloïdes aigües. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS432

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, Université Paris-Saclay (ComUE)

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). Université Paris-Saclay (ComUE). 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, Université Paris-Saclay (ComUE). Accessed November 26, 2020. 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. 26 Nov 2020.

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]. Université Paris-Saclay (ComUE); 2015. [cited 2020 Nov 26]. 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]. Université Paris-Saclay (ComUE); 2015. Available from: http://www.theses.fr/2015SACLS155

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

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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

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

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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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


Université de Bordeaux I

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

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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

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