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You searched for subject:(endosomal escape). Showing records 1 – 22 of 22 total matches.

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Texas A&M University

1. Shrestha, Ritu 1984-. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.

Degree: 2012, Texas A&M University

 Applications of nanotechnology in medicine, also known as nanomedicine, is a rapidly growing field as it holds great potential in the development of novel therapeutics… (more)

Subjects/Keywords: siRNA delivery; nanomedicine; endosomal escape; nanoparticles; Polymers

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APA (6th Edition):

Shrestha, R. 1. (2012). Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148332

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):

Shrestha, Ritu 1984-. “Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.” 2012. Thesis, Texas A&M University. Accessed November 11, 2019. http://hdl.handle.net/1969.1/148332.

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

MLA Handbook (7th Edition):

Shrestha, Ritu 1984-. “Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.” 2012. Web. 11 Nov 2019.

Vancouver:

Shrestha R1. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1969.1/148332.

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

Council of Science Editors:

Shrestha R1. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148332

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


Vanderbilt University

2. Evans, Brian Connor. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.

Degree: PhD, Biomedical Engineering, 2015, Vanderbilt University

 Peptide-based therapeutics hold significant therapeutic potential for use in a variety of clinical applications ranging from cancer to cardiovascular disease. However, the potential of peptide-based… (more)

Subjects/Keywords: intimal hyperplasia; peptide; drug delivery; endosomal escape; polyplex; nanoparticle

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APA (6th Edition):

Evans, B. C. (2015). Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;

Chicago Manual of Style (16th Edition):

Evans, Brian Connor. “Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed November 11, 2019. http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;.

MLA Handbook (7th Edition):

Evans, Brian Connor. “Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.” 2015. Web. 11 Nov 2019.

Vancouver:

Evans BC. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Nov 11]. Available from: http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;.

Council of Science Editors:

Evans BC. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu//available/etd-03182015-162324/ ;


University of Toronto

3. Broad, Amaalia. A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells.

Degree: 2009, University of Toronto

The delivery of biomolecules by cell penetrating peptides (CPPs) is an innovative therapeutic strategy. However delivery efficiency is hindered by the entrapment of CPPs in… (more)

Subjects/Keywords: Drug Delivery; Endosomal Escape; 0491

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APA (6th Edition):

Broad, A. (2009). A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/18890

Chicago Manual of Style (16th Edition):

Broad, Amaalia. “A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells.” 2009. Masters Thesis, University of Toronto. Accessed November 11, 2019. http://hdl.handle.net/1807/18890.

MLA Handbook (7th Edition):

Broad, Amaalia. “A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells.” 2009. Web. 11 Nov 2019.

Vancouver:

Broad A. A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1807/18890.

Council of Science Editors:

Broad A. A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/18890


University of New South Wales

4. Sevimli, Sema. Cholesterol conjugated polymers as therapeutic delivery vehicles : correlation between physicochemical and biological properties.

Degree: Chemical Sciences & Engineering, 2013, University of New South Wales

 The use of nano-sized synthetic polymers, comprised of therapeutic entities like drugs, genes or peptides, in clinical development has established polymer therapeutics as a credible… (more)

Subjects/Keywords: endosomal escape; cholesterol; reversible-addition fragmentation chain transfer (RAFT) polymerization; siRNA delivery

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APA (6th Edition):

Sevimli, S. (2013). Cholesterol conjugated polymers as therapeutic delivery vehicles : correlation between physicochemical and biological properties. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52710 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11383/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Sevimli, Sema. “Cholesterol conjugated polymers as therapeutic delivery vehicles : correlation between physicochemical and biological properties.” 2013. Doctoral Dissertation, University of New South Wales. Accessed November 11, 2019. http://handle.unsw.edu.au/1959.4/52710 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11383/SOURCE01?view=true.

MLA Handbook (7th Edition):

Sevimli, Sema. “Cholesterol conjugated polymers as therapeutic delivery vehicles : correlation between physicochemical and biological properties.” 2013. Web. 11 Nov 2019.

Vancouver:

Sevimli S. Cholesterol conjugated polymers as therapeutic delivery vehicles : correlation between physicochemical and biological properties. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2019 Nov 11]. Available from: http://handle.unsw.edu.au/1959.4/52710 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11383/SOURCE01?view=true.

Council of Science Editors:

Sevimli S. Cholesterol conjugated polymers as therapeutic delivery vehicles : correlation between physicochemical and biological properties. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/52710 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:11383/SOURCE01?view=true

5. Mebarek, Naila. Optimisation d'un vecteur en immunothérapie avec les cellules dendritiques : micelles de copolymères à blocs double-hydrophiles : Optimization of a vector for immunotherapy with dendritic cells : double hydrophilic block copolymer micelles.

Degree: Docteur es, Chimie et Physicochimie des matériaux, 2013, Université Montpellier I

L'objectif de cette thèse repose sur le développement de micelles de polymères polyioniques, vecteurs de molécules thérapeutiques en immunothérapie avec des cellules dendritiques (DCs). Elles… (more)

Subjects/Keywords: Micelles; Cellules dendritiques; Poly methacrylique acide bloc copolymères; Présentation d'antigène; Echappement endosomal; ARN interférence; Micelles; Dendritic cells; Polymethacrylic acid copolymers; Antigen presentation; Endosomal escape; RNA interference; 576

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APA (6th Edition):

Mebarek, N. (2013). Optimisation d'un vecteur en immunothérapie avec les cellules dendritiques : micelles de copolymères à blocs double-hydrophiles : Optimization of a vector for immunotherapy with dendritic cells : double hydrophilic block copolymer micelles. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2013MON13526

Chicago Manual of Style (16th Edition):

Mebarek, Naila. “Optimisation d'un vecteur en immunothérapie avec les cellules dendritiques : micelles de copolymères à blocs double-hydrophiles : Optimization of a vector for immunotherapy with dendritic cells : double hydrophilic block copolymer micelles.” 2013. Doctoral Dissertation, Université Montpellier I. Accessed November 11, 2019. http://www.theses.fr/2013MON13526.

MLA Handbook (7th Edition):

Mebarek, Naila. “Optimisation d'un vecteur en immunothérapie avec les cellules dendritiques : micelles de copolymères à blocs double-hydrophiles : Optimization of a vector for immunotherapy with dendritic cells : double hydrophilic block copolymer micelles.” 2013. Web. 11 Nov 2019.

Vancouver:

Mebarek N. Optimisation d'un vecteur en immunothérapie avec les cellules dendritiques : micelles de copolymères à blocs double-hydrophiles : Optimization of a vector for immunotherapy with dendritic cells : double hydrophilic block copolymer micelles. [Internet] [Doctoral dissertation]. Université Montpellier I; 2013. [cited 2019 Nov 11]. Available from: http://www.theses.fr/2013MON13526.

Council of Science Editors:

Mebarek N. Optimisation d'un vecteur en immunothérapie avec les cellules dendritiques : micelles de copolymères à blocs double-hydrophiles : Optimization of a vector for immunotherapy with dendritic cells : double hydrophilic block copolymer micelles. [Doctoral Dissertation]. Université Montpellier I; 2013. Available from: http://www.theses.fr/2013MON13526


The Ohio State University

6. Qian, Ziqing. Developments and Applications of Cyclic Cell Penetrating Peptides.

Degree: PhD, Chemistry, 2014, The Ohio State University

 Cell penetrating peptides (CPP) have been featured as a powerful delivery vector for the intracellular delivery of membrane-impermeable cargoes. This dissertation primarily focuses on the… (more)

Subjects/Keywords: Chemistry; Cell Penetrating Peptide; Drug delivery; cyclic peptide; cyclic cell penetrating peptide; protein delivery; endosomal escape; calcineurin; VIVIT

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APA (6th Edition):

Qian, Z. (2014). Developments and Applications of Cyclic Cell Penetrating Peptides. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891

Chicago Manual of Style (16th Edition):

Qian, Ziqing. “Developments and Applications of Cyclic Cell Penetrating Peptides.” 2014. Doctoral Dissertation, The Ohio State University. Accessed November 11, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891.

MLA Handbook (7th Edition):

Qian, Ziqing. “Developments and Applications of Cyclic Cell Penetrating Peptides.” 2014. Web. 11 Nov 2019.

Vancouver:

Qian Z. Developments and Applications of Cyclic Cell Penetrating Peptides. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2019 Nov 11]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891.

Council of Science Editors:

Qian Z. Developments and Applications of Cyclic Cell Penetrating Peptides. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1405340891


Universiteit Utrecht

7. Fretz, M.M. Strategies to improve intracellular drug delivery by targeted liposomes.

Degree: 2007, Universiteit Utrecht

 Biotechnological advances increased the number of novel macromolecular drugs and new drug targets. The latter are mostly found intracellular. Unfortunately, most of the new macromolecular… (more)

Subjects/Keywords: Farmacie; liposomes; cell-penetrating peptides; intracellular drug delivery; boron neutron capture therapy; endosomal escape; photochemical internalisation

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APA (6th Edition):

Fretz, M. M. (2007). Strategies to improve intracellular drug delivery by targeted liposomes. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/22271

Chicago Manual of Style (16th Edition):

Fretz, M M. “Strategies to improve intracellular drug delivery by targeted liposomes.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed November 11, 2019. http://dspace.library.uu.nl:8080/handle/1874/22271.

MLA Handbook (7th Edition):

Fretz, M M. “Strategies to improve intracellular drug delivery by targeted liposomes.” 2007. Web. 11 Nov 2019.

Vancouver:

Fretz MM. Strategies to improve intracellular drug delivery by targeted liposomes. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2019 Nov 11]. Available from: http://dspace.library.uu.nl:8080/handle/1874/22271.

Council of Science Editors:

Fretz MM. Strategies to improve intracellular drug delivery by targeted liposomes. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/22271

8. Hou, Kirk Kohwa. Melittin-Derived Peptides for siRNA Delivery: Mechanisms of Efficient Cytoplasmic Release.

Degree: PhD, Biology & Biomedical Sciences (Computational & Molecular Biophysics), 2015, Washington University in St. Louis

  The development of small molecules as therapeutic agents for targeted disease treatment is unable to keep up with the rapid expansion of databases cataloguing… (more)

Subjects/Keywords: drug delivery, endosomal escape, melittin, siRNA; Biology

…vectors is required to safely promote endosomal escape and delivery of siRNA to the cytoplasm… …association with the cell membrane, 5) promote endosomal escape to deliver siRNA to the… …endosomal escape with high cytotoxicity or poor endosomal escape with low cytotoxicity.55, 56… …Consequently, there is a need for new siRNA delivery technology to enable endosomal escape with… …possibly due to low endosomal escape or nanoparticle disassembly on glomerular basement membranes… 

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APA (6th Edition):

Hou, K. K. (2015). Melittin-Derived Peptides for siRNA Delivery: Mechanisms of Efficient Cytoplasmic Release. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/450

Chicago Manual of Style (16th Edition):

Hou, Kirk Kohwa. “Melittin-Derived Peptides for siRNA Delivery: Mechanisms of Efficient Cytoplasmic Release.” 2015. Doctoral Dissertation, Washington University in St. Louis. Accessed November 11, 2019. https://openscholarship.wustl.edu/art_sci_etds/450.

MLA Handbook (7th Edition):

Hou, Kirk Kohwa. “Melittin-Derived Peptides for siRNA Delivery: Mechanisms of Efficient Cytoplasmic Release.” 2015. Web. 11 Nov 2019.

Vancouver:

Hou KK. Melittin-Derived Peptides for siRNA Delivery: Mechanisms of Efficient Cytoplasmic Release. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2015. [cited 2019 Nov 11]. Available from: https://openscholarship.wustl.edu/art_sci_etds/450.

Council of Science Editors:

Hou KK. Melittin-Derived Peptides for siRNA Delivery: Mechanisms of Efficient Cytoplasmic Release. [Doctoral Dissertation]. Washington University in St. Louis; 2015. Available from: https://openscholarship.wustl.edu/art_sci_etds/450

9. Wiedman, Gregory R. Developing Membrane Active Peptides for Endosomal Escape of Macromolecules.

Degree: 2015, Johns Hopkins University

 Membrane Active Peptides (MAPs) are an important class of short protein sequences that hold the potential to be used for a number of varied purposes… (more)

Subjects/Keywords: Membrane Active Peptides; Endosomal Escape; Drug Delivery

…Cells by Large Molecules p110 Figure 7.7 Endosomal Escape of Macromolecules Caused by pHD… …can cause endosomal escape via a “proton-sponge effect”.23-25 In this case, drug molecules… …concentrating of solutes on the membrane may lead to endosomal escape. There are certain peptide… …Of the various methods to cause endosomal escape, creating a pathway for molecules to… …pores in an endosomal membrane would allow for the contents to escape quickly without having… 

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APA (6th Edition):

Wiedman, G. R. (2015). Developing Membrane Active Peptides for Endosomal Escape of Macromolecules. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37820

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):

Wiedman, Gregory R. “Developing Membrane Active Peptides for Endosomal Escape of Macromolecules.” 2015. Thesis, Johns Hopkins University. Accessed November 11, 2019. http://jhir.library.jhu.edu/handle/1774.2/37820.

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

MLA Handbook (7th Edition):

Wiedman, Gregory R. “Developing Membrane Active Peptides for Endosomal Escape of Macromolecules.” 2015. Web. 11 Nov 2019.

Vancouver:

Wiedman GR. Developing Membrane Active Peptides for Endosomal Escape of Macromolecules. [Internet] [Thesis]. Johns Hopkins University; 2015. [cited 2019 Nov 11]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37820.

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

Council of Science Editors:

Wiedman GR. Developing Membrane Active Peptides for Endosomal Escape of Macromolecules. [Thesis]. Johns Hopkins University; 2015. Available from: http://jhir.library.jhu.edu/handle/1774.2/37820

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

10. LO SEONG LOONG. Multifuctional peptides as biocompatible non-viral vectors for gene delivery.

Degree: 2007, National University of Singapore

Subjects/Keywords: peptide; Tat; polyethylenimine; histidine; endosomal escape; gene delivery system

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APA (6th Edition):

LOONG, L. S. (2007). Multifuctional peptides as biocompatible non-viral vectors for gene delivery. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/23102

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):

LOONG, LO SEONG. “Multifuctional peptides as biocompatible non-viral vectors for gene delivery.” 2007. Thesis, National University of Singapore. Accessed November 11, 2019. http://scholarbank.nus.edu.sg/handle/10635/23102.

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

MLA Handbook (7th Edition):

LOONG, LO SEONG. “Multifuctional peptides as biocompatible non-viral vectors for gene delivery.” 2007. Web. 11 Nov 2019.

Vancouver:

LOONG LS. Multifuctional peptides as biocompatible non-viral vectors for gene delivery. [Internet] [Thesis]. National University of Singapore; 2007. [cited 2019 Nov 11]. Available from: http://scholarbank.nus.edu.sg/handle/10635/23102.

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

Council of Science Editors:

LOONG LS. Multifuctional peptides as biocompatible non-viral vectors for gene delivery. [Thesis]. National University of Singapore; 2007. Available from: http://scholarbank.nus.edu.sg/handle/10635/23102

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


University of Illinois – Urbana-Champaign

11. Yen, Jonathan. Materials and biological approach to gene delivery in human embryonic stem cells.

Degree: PhD, Bioengineering, 2015, University of Illinois – Urbana-Champaign

 Gene delivery is an important tool used in the study and manipulation of human pluripotent stem cells for regenerative medicine purposes. However current methods of… (more)

Subjects/Keywords: endosomal escape; hyaluronic acid; Fibroblasts; Stem Cells; Human Pluripotent Stem Cells; polypeptides; Human Embryonic Stem Cells; Gene Delivery

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APA (6th Edition):

Yen, J. (2015). Materials and biological approach to gene delivery in human embryonic stem cells. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/78586

Chicago Manual of Style (16th Edition):

Yen, Jonathan. “Materials and biological approach to gene delivery in human embryonic stem cells.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 11, 2019. http://hdl.handle.net/2142/78586.

MLA Handbook (7th Edition):

Yen, Jonathan. “Materials and biological approach to gene delivery in human embryonic stem cells.” 2015. Web. 11 Nov 2019.

Vancouver:

Yen J. Materials and biological approach to gene delivery in human embryonic stem cells. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2142/78586.

Council of Science Editors:

Yen J. Materials and biological approach to gene delivery in human embryonic stem cells. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/78586


University of Michigan

12. Kim, Na Hyung. Enhanced Gene Delivery Mediated by Incorporation of Recombinant Fusion Proteins: Listeriolysin O and Peptides Derived from Protamine.

Degree: PhD, Pharmaceutical Sciences, 2011, University of Michigan

 One of the important requirements for non-viral gene delivery systems is to achieve high levels of transfection efficiency by overcoming extracellular and intracellular barriers that… (more)

Subjects/Keywords: Non-viral Gene Delivery Vector; Listeriolysin O; Recombinant Fusion Protein; Protamine; Endosomal Escape; Pharmacy and Pharmacology; Health Sciences

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APA (6th Edition):

Kim, N. H. (2011). Enhanced Gene Delivery Mediated by Incorporation of Recombinant Fusion Proteins: Listeriolysin O and Peptides Derived from Protamine. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/84648

Chicago Manual of Style (16th Edition):

Kim, Na Hyung. “Enhanced Gene Delivery Mediated by Incorporation of Recombinant Fusion Proteins: Listeriolysin O and Peptides Derived from Protamine.” 2011. Doctoral Dissertation, University of Michigan. Accessed November 11, 2019. http://hdl.handle.net/2027.42/84648.

MLA Handbook (7th Edition):

Kim, Na Hyung. “Enhanced Gene Delivery Mediated by Incorporation of Recombinant Fusion Proteins: Listeriolysin O and Peptides Derived from Protamine.” 2011. Web. 11 Nov 2019.

Vancouver:

Kim NH. Enhanced Gene Delivery Mediated by Incorporation of Recombinant Fusion Proteins: Listeriolysin O and Peptides Derived from Protamine. [Internet] [Doctoral dissertation]. University of Michigan; 2011. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2027.42/84648.

Council of Science Editors:

Kim NH. Enhanced Gene Delivery Mediated by Incorporation of Recombinant Fusion Proteins: Listeriolysin O and Peptides Derived from Protamine. [Doctoral Dissertation]. University of Michigan; 2011. Available from: http://hdl.handle.net/2027.42/84648

13. Cordier, Céline. Internalisation cellulaire et activité biologique de PNA bloqueurs stériques de la traduction, conjugués au peptide (R/W)9 : Cellular internalization and biological activity of steric blocker PNA of translation, conjugated to the (R/W)9 peptide.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2014, Université Paris Descartes – Paris V

Les Peptide Nucleic Acids (PNA) sont des oligonucléotides antisens analogues de l’ADN, dont le squelette phosphodiester a été remplacé par un squelette pseudo-peptidique d’unités 2-aminoéthylglycine,… (more)

Subjects/Keywords: Peptide Nucleic Acids; Peptides vecteurs; Internalisation; Élongation de la traduction; Libération endosomale; Peptide Nucleic Acids; Cell Penetrating Peptides; Internalization; Translation elongation; Endosomal escape; 611.018 16

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APA (6th Edition):

Cordier, C. (2014). Internalisation cellulaire et activité biologique de PNA bloqueurs stériques de la traduction, conjugués au peptide (R/W)9 : Cellular internalization and biological activity of steric blocker PNA of translation, conjugated to the (R/W)9 peptide. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2014PA05P601

Chicago Manual of Style (16th Edition):

Cordier, Céline. “Internalisation cellulaire et activité biologique de PNA bloqueurs stériques de la traduction, conjugués au peptide (R/W)9 : Cellular internalization and biological activity of steric blocker PNA of translation, conjugated to the (R/W)9 peptide.” 2014. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed November 11, 2019. http://www.theses.fr/2014PA05P601.

MLA Handbook (7th Edition):

Cordier, Céline. “Internalisation cellulaire et activité biologique de PNA bloqueurs stériques de la traduction, conjugués au peptide (R/W)9 : Cellular internalization and biological activity of steric blocker PNA of translation, conjugated to the (R/W)9 peptide.” 2014. Web. 11 Nov 2019.

Vancouver:

Cordier C. Internalisation cellulaire et activité biologique de PNA bloqueurs stériques de la traduction, conjugués au peptide (R/W)9 : Cellular internalization and biological activity of steric blocker PNA of translation, conjugated to the (R/W)9 peptide. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2014. [cited 2019 Nov 11]. Available from: http://www.theses.fr/2014PA05P601.

Council of Science Editors:

Cordier C. Internalisation cellulaire et activité biologique de PNA bloqueurs stériques de la traduction, conjugués au peptide (R/W)9 : Cellular internalization and biological activity of steric blocker PNA of translation, conjugated to the (R/W)9 peptide. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2014. Available from: http://www.theses.fr/2014PA05P601


University of Michigan

14. Vaidyanathan, Sriram. Disruption of Endosomal Membrane by Cationic Vectors Drives Endosomal Release and Enables Successful Gene Delivery.

Degree: PhD, Biomedical Engineering, 2016, University of Michigan

 The potential of gene therapy to treat congenital disorders is hindered by the lack of safe and effective delivery agents (vectors). More effective viral vectors… (more)

Subjects/Keywords: Gene delivery; Gene therapy; Endosomal escape; Drug delivery; Proton sponge; siRNA delivery; Biomedical Engineering; Biological Chemistry; Chemistry; Science (General); Engineering; Health Sciences; Science

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

APA (6th Edition):

Vaidyanathan, S. (2016). Disruption of Endosomal Membrane by Cationic Vectors Drives Endosomal Release and Enables Successful Gene Delivery. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120751

Chicago Manual of Style (16th Edition):

Vaidyanathan, Sriram. “Disruption of Endosomal Membrane by Cationic Vectors Drives Endosomal Release and Enables Successful Gene Delivery.” 2016. Doctoral Dissertation, University of Michigan. Accessed November 11, 2019. http://hdl.handle.net/2027.42/120751.

MLA Handbook (7th Edition):

Vaidyanathan, Sriram. “Disruption of Endosomal Membrane by Cationic Vectors Drives Endosomal Release and Enables Successful Gene Delivery.” 2016. Web. 11 Nov 2019.

Vancouver:

Vaidyanathan S. Disruption of Endosomal Membrane by Cationic Vectors Drives Endosomal Release and Enables Successful Gene Delivery. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2027.42/120751.

Council of Science Editors:

Vaidyanathan S. Disruption of Endosomal Membrane by Cationic Vectors Drives Endosomal Release and Enables Successful Gene Delivery. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120751


Freie Universität Berlin

15. Weng, Alexander. Investigations on saponins as membran-transfer-enhancers for proteins.

Degree: 2009, Freie Universität Berlin

 Triterpenoid saponins from Gypsophila paniculata L. are known to enhance the cytotoxicity of type I ribosome-inactivating proteins (type I RIP). These proteins exhibit N-glycosidase activity… (more)

Subjects/Keywords: saponins; type I Rip; cytotoxicity; endosomal escape; 500 Naturwissenschaften und Mathematik::540 Chemie

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APA (6th Edition):

Weng, A. (2009). Investigations on saponins as membran-transfer-enhancers for proteins. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/11786

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):

Weng, Alexander. “Investigations on saponins as membran-transfer-enhancers for proteins.” 2009. Thesis, Freie Universität Berlin. Accessed November 11, 2019. https://refubium.fu-berlin.de/handle/fub188/11786.

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

MLA Handbook (7th Edition):

Weng, Alexander. “Investigations on saponins as membran-transfer-enhancers for proteins.” 2009. Web. 11 Nov 2019.

Vancouver:

Weng A. Investigations on saponins as membran-transfer-enhancers for proteins. [Internet] [Thesis]. Freie Universität Berlin; 2009. [cited 2019 Nov 11]. Available from: https://refubium.fu-berlin.de/handle/fub188/11786.

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

Council of Science Editors:

Weng A. Investigations on saponins as membran-transfer-enhancers for proteins. [Thesis]. Freie Universität Berlin; 2009. Available from: https://refubium.fu-berlin.de/handle/fub188/11786

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


Université de Montréal

16. Viricel, Warren. Nanoparticules lipidiques pH-sensibles basées sur une bascule moléculaire pour la délivrance intracytoplasmique de siRNA .

Degree: 2017, Université de Montréal

 La délivrance intracytoplasmique de petites molécules hydrophiles et de gènes (ADN, ARN) est un défi majeur pour l’industrie pharmaceutique, puisque ces composés sont incapables de… (more)

Subjects/Keywords: Lipides; pH-sensibilité; Bascule moléculaire; Thérapie génique; Liposomes; Nanoparticules lipidiques; Echappement endosomal; Délivrance de drogues; Délivrance de siRNA; Lipids; pH-sensitive; Molecular switch; Gene therapy; Lipid nanoparticles; Endosomal escape; Drug delivery; siRNA delivery; siRNA

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

APA (6th Edition):

Viricel, W. (2017). Nanoparticules lipidiques pH-sensibles basées sur une bascule moléculaire pour la délivrance intracytoplasmique de siRNA . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/18594

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):

Viricel, Warren. “Nanoparticules lipidiques pH-sensibles basées sur une bascule moléculaire pour la délivrance intracytoplasmique de siRNA .” 2017. Thesis, Université de Montréal. Accessed November 11, 2019. http://hdl.handle.net/1866/18594.

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

MLA Handbook (7th Edition):

Viricel, Warren. “Nanoparticules lipidiques pH-sensibles basées sur une bascule moléculaire pour la délivrance intracytoplasmique de siRNA .” 2017. Web. 11 Nov 2019.

Vancouver:

Viricel W. Nanoparticules lipidiques pH-sensibles basées sur une bascule moléculaire pour la délivrance intracytoplasmique de siRNA . [Internet] [Thesis]. Université de Montréal; 2017. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/1866/18594.

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

Council of Science Editors:

Viricel W. Nanoparticules lipidiques pH-sensibles basées sur une bascule moléculaire pour la délivrance intracytoplasmique de siRNA . [Thesis]. Université de Montréal; 2017. Available from: http://hdl.handle.net/1866/18594

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

17. Shivanna, Vinay. Studies on entry events during calicivirus replication.

Degree: PhD, Department of Diagnostic Medicine and Pathobiology, 2015, Kansas State University

 Caliciviruses are important pathogens of humans and animals. Noroviruses are major causes of foodborne gastroenteritis cases, but their research is hindered due to the inability… (more)

Subjects/Keywords: Calicivirus; Bile acid; Endosomal escape; Cathepsin; Endosomal acidification; Acid sphingomyelinase; Virology (0720)

…28 1.8 Endosomal escape… …165 Ceramide formation in cells is required for endosomal escape of calicivirus… …53 Figure 1-4. Sites of Endosomal escape of viruses… …25 1.7 Endosomal proteases involved in virus uncoating… …97 Bile acid is required for PEC escape from the late endosomes into the cytoplasm… 

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APA (6th Edition):

Shivanna, V. (2015). Studies on entry events during calicivirus replication. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/18801

Chicago Manual of Style (16th Edition):

Shivanna, Vinay. “Studies on entry events during calicivirus replication.” 2015. Doctoral Dissertation, Kansas State University. Accessed November 11, 2019. http://hdl.handle.net/2097/18801.

MLA Handbook (7th Edition):

Shivanna, Vinay. “Studies on entry events during calicivirus replication.” 2015. Web. 11 Nov 2019.

Vancouver:

Shivanna V. Studies on entry events during calicivirus replication. [Internet] [Doctoral dissertation]. Kansas State University; 2015. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/2097/18801.

Council of Science Editors:

Shivanna V. Studies on entry events during calicivirus replication. [Doctoral Dissertation]. Kansas State University; 2015. Available from: http://hdl.handle.net/2097/18801


University of Illinois – Chicago

18. Rivera Vera, Claudia Ivette. Peptide-Based Strategies of Delivering Semiconductor Nanocrystals into Living Cells.

Degree: 2017, University of Illinois – Chicago

 Semiconductor nanocrystals or quantum dots (QDs) possess exceptional optical and physicochemical properties, for instance, their brightness and long fluorescence lifetimes, which makes them valuable for… (more)

Subjects/Keywords: Quantum dots; endosomal escape ability; rhodamine; FRET; CPP; HA2; Aurein 1.2; HAfp23; Palmitoyl; SPPS; glutathione; endosomolytic; imaging; confocal microscopy; TAT; TAT-HA2; polyarginine; spermine; polyamine; ratiometric FRET; FRET donor; FRET acceptor; dark quencher; BHQ-2; QSY-7; QSY-21; facilitated delivery of QDs; synthesis; MALDI

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APA (6th Edition):

Rivera Vera, C. I. (2017). Peptide-Based Strategies of Delivering Semiconductor Nanocrystals into Living Cells. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22251

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):

Rivera Vera, Claudia Ivette. “Peptide-Based Strategies of Delivering Semiconductor Nanocrystals into Living Cells.” 2017. Thesis, University of Illinois – Chicago. Accessed November 11, 2019. http://hdl.handle.net/10027/22251.

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

MLA Handbook (7th Edition):

Rivera Vera, Claudia Ivette. “Peptide-Based Strategies of Delivering Semiconductor Nanocrystals into Living Cells.” 2017. Web. 11 Nov 2019.

Vancouver:

Rivera Vera CI. Peptide-Based Strategies of Delivering Semiconductor Nanocrystals into Living Cells. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Nov 11]. Available from: http://hdl.handle.net/10027/22251.

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

Council of Science Editors:

Rivera Vera CI. Peptide-Based Strategies of Delivering Semiconductor Nanocrystals into Living Cells. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22251

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

19. Fretz, M.M. Strategies to improve intracellular drug delivery by targeted liposomes.

Degree: 2007, University Utrecht

 Biotechnological advances increased the number of novel macromolecular drugs and new drug targets. The latter are mostly found intracellular. Unfortunately, most of the new macromolecular… (more)

Subjects/Keywords: liposomes; cell-penetrating peptides; intracellular drug delivery; boron neutron capture therapy; endosomal escape; photochemical internalisation

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APA (6th Edition):

Fretz, M. M. (2007). Strategies to improve intracellular drug delivery by targeted liposomes. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/22271 ; URN:NBN:NL:UI:10-1874-22271 ; urn:isbn:90-393-4521-4 ; URN:NBN:NL:UI:10-1874-22271 ; http://dspace.library.uu.nl/handle/1874/22271

Chicago Manual of Style (16th Edition):

Fretz, M M. “Strategies to improve intracellular drug delivery by targeted liposomes.” 2007. Doctoral Dissertation, University Utrecht. Accessed November 11, 2019. http://dspace.library.uu.nl/handle/1874/22271 ; URN:NBN:NL:UI:10-1874-22271 ; urn:isbn:90-393-4521-4 ; URN:NBN:NL:UI:10-1874-22271 ; http://dspace.library.uu.nl/handle/1874/22271.

MLA Handbook (7th Edition):

Fretz, M M. “Strategies to improve intracellular drug delivery by targeted liposomes.” 2007. Web. 11 Nov 2019.

Vancouver:

Fretz MM. Strategies to improve intracellular drug delivery by targeted liposomes. [Internet] [Doctoral dissertation]. University Utrecht; 2007. [cited 2019 Nov 11]. Available from: http://dspace.library.uu.nl/handle/1874/22271 ; URN:NBN:NL:UI:10-1874-22271 ; urn:isbn:90-393-4521-4 ; URN:NBN:NL:UI:10-1874-22271 ; http://dspace.library.uu.nl/handle/1874/22271.

Council of Science Editors:

Fretz MM. Strategies to improve intracellular drug delivery by targeted liposomes. [Doctoral Dissertation]. University Utrecht; 2007. Available from: http://dspace.library.uu.nl/handle/1874/22271 ; URN:NBN:NL:UI:10-1874-22271 ; urn:isbn:90-393-4521-4 ; URN:NBN:NL:UI:10-1874-22271 ; http://dspace.library.uu.nl/handle/1874/22271


Freie Universität Berlin

20. Gilabert-Oriol, Roger. Entwicklung einer Plattformtechnologie zur verstärkten endo/lysosomalen Freisetzung von zielgerichteten Toxinen mittels strukturspezifischer oleananer Saponine.

Degree: 2014, Freie Universität Berlin

 Zielgerichtete Toxine sind proteinbasierte Therapeutika, die im Hinblick auf ihre Anwendung in der zielgerichteten Tumortherapie erforscht werden. Sie bestehen aus einem toxischen Enzym, zum Beispiel… (more)

Subjects/Keywords: endosomal escape; targeted toxin; immunotoxin; oleanane saponin; platform technology; 500 Naturwissenschaften und Mathematik::500 Naturwissenschaften; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik

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APA (6th Edition):

Gilabert-Oriol, R. (2014). Entwicklung einer Plattformtechnologie zur verstärkten endo/lysosomalen Freisetzung von zielgerichteten Toxinen mittels strukturspezifischer oleananer Saponine. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-7621

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):

Gilabert-Oriol, Roger. “Entwicklung einer Plattformtechnologie zur verstärkten endo/lysosomalen Freisetzung von zielgerichteten Toxinen mittels strukturspezifischer oleananer Saponine.” 2014. Thesis, Freie Universität Berlin. Accessed November 11, 2019. http://dx.doi.org/10.17169/refubium-7621.

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

MLA Handbook (7th Edition):

Gilabert-Oriol, Roger. “Entwicklung einer Plattformtechnologie zur verstärkten endo/lysosomalen Freisetzung von zielgerichteten Toxinen mittels strukturspezifischer oleananer Saponine.” 2014. Web. 11 Nov 2019.

Vancouver:

Gilabert-Oriol R. Entwicklung einer Plattformtechnologie zur verstärkten endo/lysosomalen Freisetzung von zielgerichteten Toxinen mittels strukturspezifischer oleananer Saponine. [Internet] [Thesis]. Freie Universität Berlin; 2014. [cited 2019 Nov 11]. Available from: http://dx.doi.org/10.17169/refubium-7621.

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

Council of Science Editors:

Gilabert-Oriol R. Entwicklung einer Plattformtechnologie zur verstärkten endo/lysosomalen Freisetzung von zielgerichteten Toxinen mittels strukturspezifischer oleananer Saponine. [Thesis]. Freie Universität Berlin; 2014. Available from: http://dx.doi.org/10.17169/refubium-7621

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


Freie Universität Berlin

21. Sama, Simko. Investigation of saponins as novel transfection enhancer.

Degree: 2018, Freie Universität Berlin

 Die Fähigkeit bestimmter Triterpensaponine als Mediator des endosomalen Release zu agieren, wurde in der Vergangenheit intensiv beforscht. Durch Interaktion mit der Endosomenmembran sind diese Sekundärstoffe… (more)

Subjects/Keywords: Transfektion; Saponine; Endosomaler Release; Transfektionsverstärker; Suizidgentherapie; Endosomal escape; transfection enhancer; suicide gene therapy; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::615 Pharmakologie, Therapeutik; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::576 Genetik und Evolution

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APA (6th Edition):

Sama, S. (2018). Investigation of saponins as novel transfection enhancer. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-15

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):

Sama, Simko. “Investigation of saponins as novel transfection enhancer.” 2018. Thesis, Freie Universität Berlin. Accessed November 11, 2019. http://dx.doi.org/10.17169/refubium-15.

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

MLA Handbook (7th Edition):

Sama, Simko. “Investigation of saponins as novel transfection enhancer.” 2018. Web. 11 Nov 2019.

Vancouver:

Sama S. Investigation of saponins as novel transfection enhancer. [Internet] [Thesis]. Freie Universität Berlin; 2018. [cited 2019 Nov 11]. Available from: http://dx.doi.org/10.17169/refubium-15.

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

Council of Science Editors:

Sama S. Investigation of saponins as novel transfection enhancer. [Thesis]. Freie Universität Berlin; 2018. Available from: http://dx.doi.org/10.17169/refubium-15

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


Université Paris-Sud – Paris XI

22. Garcia-Castillo, Maria Daniela. Mechanisms of Endosomal Membrane Translocation Leading to Antigen Cross-presentation : Mécanismes de translocation de membrane endosomale menant à l'antigène présentation croisée.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2014, Université Paris-Sud – Paris XI

Dans l'introduction, diverses voies de trafic intracellulaire et endocytose seront discutées. Je familiarise le lecteur avec des protéines inactivant les ribosomes, en mettant l'accent sur… (more)

Subjects/Keywords: Transport rétrograde; Immunothérapie; Cellules dendritiques; Cholestérol; Rab7; Présentation d’antigène croisée; Petites molécules inhibiteurs; Petites molécules activateurs; Endosomal; STxB - saporine; Spectrométrie de masse; Petite Identification d’une cible d’une petite molécule; Chimie click; Syntaxine-5; Génétique chimique; Rétro-2; STxB; Retrograde transport; Immunotherapy; Dendritic cells; Cholesterol; Rab7; Antigen cross-presentation; Small molecule inhibitors; Small molecule activators; Endosomal escape; STxB-saporin conjugates; Mass spectrometry; Small molecule target identification; Copper-free click chemistry; Syntaxin-5; Chemical genetics; Retro-2; STxB

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

APA (6th Edition):

Garcia-Castillo, M. D. (2014). Mechanisms of Endosomal Membrane Translocation Leading to Antigen Cross-presentation : Mécanismes de translocation de membrane endosomale menant à l'antigène présentation croisée. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA11T075

Chicago Manual of Style (16th Edition):

Garcia-Castillo, Maria Daniela. “Mechanisms of Endosomal Membrane Translocation Leading to Antigen Cross-presentation : Mécanismes de translocation de membrane endosomale menant à l'antigène présentation croisée.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed November 11, 2019. http://www.theses.fr/2014PA11T075.

MLA Handbook (7th Edition):

Garcia-Castillo, Maria Daniela. “Mechanisms of Endosomal Membrane Translocation Leading to Antigen Cross-presentation : Mécanismes de translocation de membrane endosomale menant à l'antigène présentation croisée.” 2014. Web. 11 Nov 2019.

Vancouver:

Garcia-Castillo MD. Mechanisms of Endosomal Membrane Translocation Leading to Antigen Cross-presentation : Mécanismes de translocation de membrane endosomale menant à l'antigène présentation croisée. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2019 Nov 11]. Available from: http://www.theses.fr/2014PA11T075.

Council of Science Editors:

Garcia-Castillo MD. Mechanisms of Endosomal Membrane Translocation Leading to Antigen Cross-presentation : Mécanismes de translocation de membrane endosomale menant à l'antigène présentation croisée. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA11T075

.