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You searched for subject:(siRNA delivery). Showing records 1 – 30 of 95 total matches.

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Penn State University

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

Degree: MS, Bioengineering, 2012, Penn State University

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Masters Thesis, Penn State University. Accessed September 17, 2019. https://etda.libraries.psu.edu/catalog/15235.

MLA Handbook (7th Edition):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Web. 17 Sep 2019.

Vancouver:

Sutermaster BA. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. [Internet] [Masters thesis]. Penn State University; 2012. [cited 2019 Sep 17]. Available from: https://etda.libraries.psu.edu/catalog/15235.

Council of Science Editors:

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


Cornell University

2. Pelet, Jeisa. Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation .

Degree: 2011, Cornell University

 Gene therapy has emerged as a promising technique to treat many chronic diseases, genetic disorders and even cancer. Furthermore, the recent discovery that RNA interference… (more)

Subjects/Keywords: polymers; combinatorial libraries; siRNA delivery

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APA (6th Edition):

Pelet, J. (2011). Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29360

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):

Pelet, Jeisa. “Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation .” 2011. Thesis, Cornell University. Accessed September 17, 2019. http://hdl.handle.net/1813/29360.

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

MLA Handbook (7th Edition):

Pelet, Jeisa. “Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation .” 2011. Web. 17 Sep 2019.

Vancouver:

Pelet J. Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation . [Internet] [Thesis]. Cornell University; 2011. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/1813/29360.

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

Council of Science Editors:

Pelet J. Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29360

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


University of Debrecen

3. Koohestanu, Sina. Advanced siRNA delivery system .

Degree: DE – Gyógyszerésztudományi Kar, University of Debrecen

small interfering RNA which down regulate gene expression guided by sequence complementarity , can be used therapeutically to block the synthesis of disease causing proteins.siRNA play an essential role in treatment of cancer.the basic mechanism is the RNA interference. Advisors/Committee Members: Fenyvesi, Ferenc (advisor).

Subjects/Keywords: siRNA delivery

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APA (6th Edition):

Koohestanu, S. (n.d.). Advanced siRNA delivery system . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/241046

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Koohestanu, Sina. “Advanced siRNA delivery system .” Thesis, University of Debrecen. Accessed September 17, 2019. http://hdl.handle.net/2437/241046.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Koohestanu, Sina. “Advanced siRNA delivery system .” Web. 17 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Koohestanu S. Advanced siRNA delivery system . [Internet] [Thesis]. University of Debrecen; [cited 2019 Sep 17]. Available from: http://hdl.handle.net/2437/241046.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Koohestanu S. Advanced siRNA delivery system . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/241046

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Manchester

4. Frede, Annika. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.

Degree: PhD, 2016, University of Manchester

 In this thesis nanoparticles consisting of a calcium phosphate core encapsulated by poly(lactic-co-glycolic) acid and polyethylenimine were developed for the delivery of siRNA in vivo.… (more)

Subjects/Keywords: siRNA delivery; nanoparticles; IBD; COPD

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APA (6th Edition):

Frede, A. (2016). Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458

Chicago Manual of Style (16th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 17, 2019. https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458.

MLA Handbook (7th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Web. 17 Sep 2019.

Vancouver:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458.

Council of Science Editors:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458


University of Manchester

5. Frede, Annika. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.

Degree: 2016, University of Manchester

 In this thesis nanoparticles consisting of a calcium phosphate core encapsulated by poly(lactic-co-glycolic) acid and polyethylenimine were developed for the delivery of siRNA in vivo.… (more)

Subjects/Keywords: siRNA delivery; nanoparticles; IBD; COPD

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APA (6th Edition):

Frede, A. (2016). Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897

Chicago Manual of Style (16th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Doctoral Dissertation, University of Manchester. Accessed September 17, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897.

MLA Handbook (7th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Web. 17 Sep 2019.

Vancouver:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Sep 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897.

Council of Science Editors:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897


Johannes Gutenberg Universität Mainz

6. Krieg, Bettina Sarah. Evaluation of polymeric nanocarriers for RNA delivery.

Degree: 2014, Johannes Gutenberg Universität Mainz

Therapeutic RNAs, especially siRNAs, are a promising approach for treating diseases like cancer, neurodegenerative disorders and viral infections. Their application, however, is limited due to… (more)

Subjects/Keywords: siRNA; polyplexes; delivery; siRNA; Polyplexe; Transport; Natural sciences and mathematics

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APA (6th Edition):

Krieg, B. S. (2014). Evaluation of polymeric nanocarriers for RNA delivery. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/

Chicago Manual of Style (16th Edition):

Krieg, Bettina Sarah. “Evaluation of polymeric nanocarriers for RNA delivery.” 2014. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 17, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/.

MLA Handbook (7th Edition):

Krieg, Bettina Sarah. “Evaluation of polymeric nanocarriers for RNA delivery.” 2014. Web. 17 Sep 2019.

Vancouver:

Krieg BS. Evaluation of polymeric nanocarriers for RNA delivery. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2014. [cited 2019 Sep 17]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/.

Council of Science Editors:

Krieg BS. Evaluation of polymeric nanocarriers for RNA delivery. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2014. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/


University of Alberta

7. Alshamsan, Aws. Development of stat-3 targeting siRNA nano-carriers for cancer therapy.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2010, University of Alberta

 In many tumors, persistently-active signal transducer and activator of transcription 3 (STAT3) imparts several oncogenic features such as survival, proliferation, angiogenesis, and immune escape. Therefore,… (more)

Subjects/Keywords: STAT-3; Cancer; siRNA; Nanomedicine; Drug Delivery

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APA (6th Edition):

Alshamsan, A. (2010). Development of stat-3 targeting siRNA nano-carriers for cancer therapy. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/fx719n70b

Chicago Manual of Style (16th Edition):

Alshamsan, Aws. “Development of stat-3 targeting siRNA nano-carriers for cancer therapy.” 2010. Doctoral Dissertation, University of Alberta. Accessed September 17, 2019. https://era.library.ualberta.ca/files/fx719n70b.

MLA Handbook (7th Edition):

Alshamsan, Aws. “Development of stat-3 targeting siRNA nano-carriers for cancer therapy.” 2010. Web. 17 Sep 2019.

Vancouver:

Alshamsan A. Development of stat-3 targeting siRNA nano-carriers for cancer therapy. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2019 Sep 17]. Available from: https://era.library.ualberta.ca/files/fx719n70b.

Council of Science Editors:

Alshamsan A. Development of stat-3 targeting siRNA nano-carriers for cancer therapy. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/fx719n70b


Texas A&M University

8. 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 September 17, 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. 17 Sep 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 Sep 17]. 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

9. Jackson, Meredith Allyn. Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery.

Degree: MS, Biomedical Engineering, 2016, Vanderbilt University

 Although siRNA-based therapeutics hold great promise for systemic cancer treatment, polyplex nanocarrier systems face many intravenous challenges that limit their pharmacokinetic potential and therefore reduce… (more)

Subjects/Keywords: siRNA; pharmacokinetics; zwitterionic materials; polyplexes; drug delivery

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APA (6th Edition):

Jackson, M. A. (2016). Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-11172016-131552/ ;

Chicago Manual of Style (16th Edition):

Jackson, Meredith Allyn. “Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery.” 2016. Masters Thesis, Vanderbilt University. Accessed September 17, 2019. http://etd.library.vanderbilt.edu//available/etd-11172016-131552/ ;.

MLA Handbook (7th Edition):

Jackson, Meredith Allyn. “Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery.” 2016. Web. 17 Sep 2019.

Vancouver:

Jackson MA. Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery. [Internet] [Masters thesis]. Vanderbilt University; 2016. [cited 2019 Sep 17]. Available from: http://etd.library.vanderbilt.edu//available/etd-11172016-131552/ ;.

Council of Science Editors:

Jackson MA. Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery. [Masters Thesis]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu//available/etd-11172016-131552/ ;


University of Waterloo

10. Pan, Ran. Stearylated Peptides for Therapeutic siRNA Delivery and Their Cellular Uptake Mechanisms.

Degree: 2015, University of Waterloo

 Small interfering RNA (siRNA) shows great potential as a powerful tool in gene therapy, due to its ability to regulate gene expression in a highly… (more)

Subjects/Keywords: siRNA; cell-penetrating peptide; RNAi; gene delivery

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APA (6th Edition):

Pan, R. (2015). Stearylated Peptides for Therapeutic siRNA Delivery and Their Cellular Uptake Mechanisms. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/9822

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):

Pan, Ran. “Stearylated Peptides for Therapeutic siRNA Delivery and Their Cellular Uptake Mechanisms.” 2015. Thesis, University of Waterloo. Accessed September 17, 2019. http://hdl.handle.net/10012/9822.

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

MLA Handbook (7th Edition):

Pan, Ran. “Stearylated Peptides for Therapeutic siRNA Delivery and Their Cellular Uptake Mechanisms.” 2015. Web. 17 Sep 2019.

Vancouver:

Pan R. Stearylated Peptides for Therapeutic siRNA Delivery and Their Cellular Uptake Mechanisms. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10012/9822.

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

Council of Science Editors:

Pan R. Stearylated Peptides for Therapeutic siRNA Delivery and Their Cellular Uptake Mechanisms. [Thesis]. University of Waterloo; 2015. Available from: http://hdl.handle.net/10012/9822

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


Vanderbilt University

11. Werfel, Thomas Anthony. Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation.

Degree: MS, Biomedical Engineering, 2015, Vanderbilt University

 A combinatorial library of ternary polyplexes was herein investigated to optimize formulations for siRNA delivery. The compositions tested build from our previous finding that balancing… (more)

Subjects/Keywords: Polyplexes; pH-responsive; intravenous delivery; siRNA

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APA (6th Edition):

Werfel, T. A. (2015). Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03202015-092139/ ;

Chicago Manual of Style (16th Edition):

Werfel, Thomas Anthony. “Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation.” 2015. Masters Thesis, Vanderbilt University. Accessed September 17, 2019. http://etd.library.vanderbilt.edu//available/etd-03202015-092139/ ;.

MLA Handbook (7th Edition):

Werfel, Thomas Anthony. “Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation.” 2015. Web. 17 Sep 2019.

Vancouver:

Werfel TA. Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation. [Internet] [Masters thesis]. Vanderbilt University; 2015. [cited 2019 Sep 17]. Available from: http://etd.library.vanderbilt.edu//available/etd-03202015-092139/ ;.

Council of Science Editors:

Werfel TA. Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation. [Masters Thesis]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu//available/etd-03202015-092139/ ;


University of Minnesota

12. Xue, Lian. Synthesis and Evaluation of Carbohydrate Based Cationic Polymers for siRNA Delivery and Tracking.

Degree: PhD, Chemistry, 2014, University of Minnesota

 Biocompatible and biodegradable macromolecules have been intensively used in pharmaceutical industries in various formulation preparations to fulfill different requirements. In the last two decades, RNA… (more)

Subjects/Keywords: biocompatible; : Carbohydrate based polymers; siRNA delivery; theranostics

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APA (6th Edition):

Xue, L. (2014). Synthesis and Evaluation of Carbohydrate Based Cationic Polymers for siRNA Delivery and Tracking. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174909

Chicago Manual of Style (16th Edition):

Xue, Lian. “Synthesis and Evaluation of Carbohydrate Based Cationic Polymers for siRNA Delivery and Tracking.” 2014. Doctoral Dissertation, University of Minnesota. Accessed September 17, 2019. http://hdl.handle.net/11299/174909.

MLA Handbook (7th Edition):

Xue, Lian. “Synthesis and Evaluation of Carbohydrate Based Cationic Polymers for siRNA Delivery and Tracking.” 2014. Web. 17 Sep 2019.

Vancouver:

Xue L. Synthesis and Evaluation of Carbohydrate Based Cationic Polymers for siRNA Delivery and Tracking. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/11299/174909.

Council of Science Editors:

Xue L. Synthesis and Evaluation of Carbohydrate Based Cationic Polymers for siRNA Delivery and Tracking. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/174909


University of Texas – Austin

13. Knipe, Jennifer Marie. Multi-responsive microencapsulated nanogels for the oral delivery of small interfering RNA.

Degree: PhD, Chemical Engineering, 2014, University of Texas – Austin

 Multi-responsive, anionic poly(methacrylic acid-co-N-vinyl-2-pyrrolidone) microscale hydrogels (microgels) encapsulating polycationic nanoscale hydrogels (nanogels) were synthesized with either degradable or nondegradable crosslinks. The pH-responsive volume phase transition… (more)

Subjects/Keywords: Hydrogel; Oral delivery; Ph-responsive; Biodegradable; SiRNA

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APA (6th Edition):

Knipe, J. M. (2014). Multi-responsive microencapsulated nanogels for the oral delivery of small interfering RNA. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46514

Chicago Manual of Style (16th Edition):

Knipe, Jennifer Marie. “Multi-responsive microencapsulated nanogels for the oral delivery of small interfering RNA.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed September 17, 2019. http://hdl.handle.net/2152/46514.

MLA Handbook (7th Edition):

Knipe, Jennifer Marie. “Multi-responsive microencapsulated nanogels for the oral delivery of small interfering RNA.” 2014. Web. 17 Sep 2019.

Vancouver:

Knipe JM. Multi-responsive microencapsulated nanogels for the oral delivery of small interfering RNA. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/2152/46514.

Council of Science Editors:

Knipe JM. Multi-responsive microencapsulated nanogels for the oral delivery of small interfering RNA. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/46514


University of Southern Mississippi

14. Shi, Yongliang. Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery.

Degree: MS, Chemistry and Biochemistry, 2014, University of Southern Mississippi

  Through layer-by-layer method, the authors have constructed three Au nanoplexes: AuPEI/RNA/PEI, AuPEI/RNA/PEI-mPEG, and AuPEI/NA/PEI-PEG-FA. All the nanoplexes are characterized by UV-vis spectrometry, DLS, and… (more)

Subjects/Keywords: gold nanoparticles; siRNA delivery; cancer-targeted delivery; Biotechnology; Medical Biochemistry; Nanomedicine

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APA (6th Edition):

Shi, Y. (2014). Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery. (Masters Thesis). University of Southern Mississippi. Retrieved from https://aquila.usm.edu/masters_theses/37

Chicago Manual of Style (16th Edition):

Shi, Yongliang. “Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery.” 2014. Masters Thesis, University of Southern Mississippi. Accessed September 17, 2019. https://aquila.usm.edu/masters_theses/37.

MLA Handbook (7th Edition):

Shi, Yongliang. “Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery.” 2014. Web. 17 Sep 2019.

Vancouver:

Shi Y. Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery. [Internet] [Masters thesis]. University of Southern Mississippi; 2014. [cited 2019 Sep 17]. Available from: https://aquila.usm.edu/masters_theses/37.

Council of Science Editors:

Shi Y. Self-Assembled Gold Nanoplexes for Cancer-Targeted siRNA Delivery. [Masters Thesis]. University of Southern Mississippi; 2014. Available from: https://aquila.usm.edu/masters_theses/37


University of Western Ontario

15. Siu, King Sun. Development of Non-Covalent Functionalization of Carbon Nanotubes for siRNA Delivery.

Degree: 2014, University of Western Ontario

 RNA interference (RNAi) therapy is promising for treating various diseases but the delivery of small interfering RNA (siRNA) is difficult. To overcome the technical difficulties… (more)

Subjects/Keywords: CNT; SWCNT; RNAi; siRNA; non-viral gene delivery; siRNA delivery; Biotechnology; Macromolecular Substances; Medical Biotechnology; Nanomedicine; Nanotechnology

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

APA (6th Edition):

Siu, K. S. (2014). Development of Non-Covalent Functionalization of Carbon Nanotubes for siRNA Delivery. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2006

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):

Siu, King Sun. “Development of Non-Covalent Functionalization of Carbon Nanotubes for siRNA Delivery.” 2014. Thesis, University of Western Ontario. Accessed September 17, 2019. https://ir.lib.uwo.ca/etd/2006.

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

MLA Handbook (7th Edition):

Siu, King Sun. “Development of Non-Covalent Functionalization of Carbon Nanotubes for siRNA Delivery.” 2014. Web. 17 Sep 2019.

Vancouver:

Siu KS. Development of Non-Covalent Functionalization of Carbon Nanotubes for siRNA Delivery. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2019 Sep 17]. Available from: https://ir.lib.uwo.ca/etd/2006.

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

Council of Science Editors:

Siu KS. Development of Non-Covalent Functionalization of Carbon Nanotubes for siRNA Delivery. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/2006

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

16. Tzeng, Stephany Yi. Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering.

Degree: 2014, Johns Hopkins University

 The fields of biomaterials, nanobiotechnology, and gene and drug delivery have all progressed over the past decades and have rapidly become a focus of research… (more)

Subjects/Keywords: nanomedicine; nanoparticles; polymeric gene delivery; non-viral gene delivery; DNA delivery; siRNA delivery; targeted cancer therapy

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

APA (6th Edition):

Tzeng, S. Y. (2014). Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/36968

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):

Tzeng, Stephany Yi. “Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering.” 2014. Thesis, Johns Hopkins University. Accessed September 17, 2019. http://jhir.library.jhu.edu/handle/1774.2/36968.

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

MLA Handbook (7th Edition):

Tzeng, Stephany Yi. “Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering.” 2014. Web. 17 Sep 2019.

Vancouver:

Tzeng SY. Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2019 Sep 17]. Available from: http://jhir.library.jhu.edu/handle/1774.2/36968.

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

Council of Science Editors:

Tzeng SY. Polymeric Nanoparticle-Based DNA AND siRNA Delivery for Cancer Treatment and Stem Cell Engineering. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/36968

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

17. Solfiell, David J. Gold Nanoparticles and Drug Delivery.

Degree: MS(M.S.), Chemistry, 2014, U of Massachusetts : Masters

  Nanoparticles are important tools in biotechnology and biomedical research. Gold nanoparticles (AuNPs) have emerged as a particularly important class of nanobiotechnological tools as a… (more)

Subjects/Keywords: Gold Nanoparticles; Drug Delivery; Hydrophobicity; Protein Delivery; Sustained Release; siRNA; Organic Chemistry

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

APA (6th Edition):

Solfiell, D. J. (2014). Gold Nanoparticles and Drug Delivery. (Masters Thesis). U of Massachusetts : Masters. Retrieved from http://scholarworks.umass.edu/theses/1200

Chicago Manual of Style (16th Edition):

Solfiell, David J. “Gold Nanoparticles and Drug Delivery.” 2014. Masters Thesis, U of Massachusetts : Masters. Accessed September 17, 2019. http://scholarworks.umass.edu/theses/1200.

MLA Handbook (7th Edition):

Solfiell, David J. “Gold Nanoparticles and Drug Delivery.” 2014. Web. 17 Sep 2019.

Vancouver:

Solfiell DJ. Gold Nanoparticles and Drug Delivery. [Internet] [Masters thesis]. U of Massachusetts : Masters; 2014. [cited 2019 Sep 17]. Available from: http://scholarworks.umass.edu/theses/1200.

Council of Science Editors:

Solfiell DJ. Gold Nanoparticles and Drug Delivery. [Masters Thesis]. U of Massachusetts : Masters; 2014. Available from: http://scholarworks.umass.edu/theses/1200


University of Waterloo

18. Xu, Wen. Endosomolytic arginine-rich peptides for therapeutic siRNA delivery.

Degree: 2014, University of Waterloo

 At the forefront of revolutionizing medicine, gene therapy provides an effective way to treat a range of diseases by regulating defective genes at the root… (more)

Subjects/Keywords: siRNA; peptide; gene delivery system; characterization; knockdown efficiency; in vivo; co-delivery

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

APA (6th Edition):

Xu, W. (2014). Endosomolytic arginine-rich peptides for therapeutic siRNA delivery. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/8580

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):

Xu, Wen. “Endosomolytic arginine-rich peptides for therapeutic siRNA delivery.” 2014. Thesis, University of Waterloo. Accessed September 17, 2019. http://hdl.handle.net/10012/8580.

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

MLA Handbook (7th Edition):

Xu, Wen. “Endosomolytic arginine-rich peptides for therapeutic siRNA delivery.” 2014. Web. 17 Sep 2019.

Vancouver:

Xu W. Endosomolytic arginine-rich peptides for therapeutic siRNA delivery. [Internet] [Thesis]. University of Waterloo; 2014. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10012/8580.

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

Council of Science Editors:

Xu W. Endosomolytic arginine-rich peptides for therapeutic siRNA delivery. [Thesis]. University of Waterloo; 2014. Available from: http://hdl.handle.net/10012/8580

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


University of Alberta

19. Sahin,B. Development of a non-viral delivery system for siRNA for treatment of lymphoma.

Degree: MS, Department of Biomedical Engineering, 2013, University of Alberta

 The aim of this work is to develop an effective non-viral carrier and to identify suitable gene targets that would induce apoptosis specifically in lymphoma… (more)

Subjects/Keywords: lymphoma; PEI; polymeric carrier; non-viral; delivery; silencing; siRNA; cancer

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

APA (6th Edition):

Sahin,B. (2013). Development of a non-viral delivery system for siRNA for treatment of lymphoma. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/kk91fm497

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

Chicago Manual of Style (16th Edition):

Sahin,B. “Development of a non-viral delivery system for siRNA for treatment of lymphoma.” 2013. Masters Thesis, University of Alberta. Accessed September 17, 2019. https://era.library.ualberta.ca/files/kk91fm497.

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

MLA Handbook (7th Edition):

Sahin,B. “Development of a non-viral delivery system for siRNA for treatment of lymphoma.” 2013. Web. 17 Sep 2019.

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

Vancouver:

Sahin,B. Development of a non-viral delivery system for siRNA for treatment of lymphoma. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2019 Sep 17]. Available from: https://era.library.ualberta.ca/files/kk91fm497.

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

Council of Science Editors:

Sahin,B. Development of a non-viral delivery system for siRNA for treatment of lymphoma. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/kk91fm497

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

20. Novo, Luís. Decationized polyplexes for targeted delivery of nucleic acids : from carrier design to in vivo evaluation.

Degree: 2014, Universiteit Utrecht

 Gene therapy is considered a promising treatment for current intractable diseases. However, the clinical applicability of gene therapy is highly dependent on the development of… (more)

Subjects/Keywords: Gene delivery; pDNA; siRNA; polymer; biocompatibility; nanoparticle; targeting; biodistribution; in vivo

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APA (6th Edition):

Novo, L. (2014). Decationized polyplexes for targeted delivery of nucleic acids : from carrier design to in vivo evaluation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/300546

Chicago Manual of Style (16th Edition):

Novo, Luís. “Decationized polyplexes for targeted delivery of nucleic acids : from carrier design to in vivo evaluation.” 2014. Doctoral Dissertation, Universiteit Utrecht. Accessed September 17, 2019. http://dspace.library.uu.nl:8080/handle/1874/300546.

MLA Handbook (7th Edition):

Novo, Luís. “Decationized polyplexes for targeted delivery of nucleic acids : from carrier design to in vivo evaluation.” 2014. Web. 17 Sep 2019.

Vancouver:

Novo L. Decationized polyplexes for targeted delivery of nucleic acids : from carrier design to in vivo evaluation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2014. [cited 2019 Sep 17]. Available from: http://dspace.library.uu.nl:8080/handle/1874/300546.

Council of Science Editors:

Novo L. Decationized polyplexes for targeted delivery of nucleic acids : from carrier design to in vivo evaluation. [Doctoral Dissertation]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/300546


Georgia Tech

21. Liu, Jie. Development of multifunctional siRNA delivery systems and their applications in modulating gene expression in a cardiac ischemia-reperfusion model.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2013, Georgia Tech

 RNA interference (RNAi) is a conservative post-transcriptional gene silencing mechanism that can be mediated by small interfering RNAs (siRNAs). Given the effectiveness and specificity of… (more)

Subjects/Keywords: Delivery system; siRNA; Cell penetrating peptide; Dendrimer; Myocardial infarction

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

APA (6th Edition):

Liu, J. (2013). Development of multifunctional siRNA delivery systems and their applications in modulating gene expression in a cardiac ischemia-reperfusion model. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53391

Chicago Manual of Style (16th Edition):

Liu, Jie. “Development of multifunctional siRNA delivery systems and their applications in modulating gene expression in a cardiac ischemia-reperfusion model.” 2013. Doctoral Dissertation, Georgia Tech. Accessed September 17, 2019. http://hdl.handle.net/1853/53391.

MLA Handbook (7th Edition):

Liu, Jie. “Development of multifunctional siRNA delivery systems and their applications in modulating gene expression in a cardiac ischemia-reperfusion model.” 2013. Web. 17 Sep 2019.

Vancouver:

Liu J. Development of multifunctional siRNA delivery systems and their applications in modulating gene expression in a cardiac ischemia-reperfusion model. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/1853/53391.

Council of Science Editors:

Liu J. Development of multifunctional siRNA delivery systems and their applications in modulating gene expression in a cardiac ischemia-reperfusion model. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/53391


Carnegie Mellon University

22. Knapp, Christopher M. Engineering siRNA Lipid Nanoparticles for the Treatment of Mantle Cell Lymphoma.

Degree: 2017, Carnegie Mellon University

 Mantle cell lymphoma (MCL) is an extremely difficult to treat subtype of non-Hodgkin lymphoma (NHL) with a low patient survival rate compared to most common… (more)

Subjects/Keywords: drug delivery; lipidoid; nanoparticle; nanotechnology; non-Hodgkin lymphoma; siRNA

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APA (6th Edition):

Knapp, C. M. (2017). Engineering siRNA Lipid Nanoparticles for the Treatment of Mantle Cell Lymphoma. (Thesis). Carnegie Mellon University. Retrieved from http://repository.cmu.edu/dissertations/886

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):

Knapp, Christopher M. “Engineering siRNA Lipid Nanoparticles for the Treatment of Mantle Cell Lymphoma.” 2017. Thesis, Carnegie Mellon University. Accessed September 17, 2019. http://repository.cmu.edu/dissertations/886.

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

MLA Handbook (7th Edition):

Knapp, Christopher M. “Engineering siRNA Lipid Nanoparticles for the Treatment of Mantle Cell Lymphoma.” 2017. Web. 17 Sep 2019.

Vancouver:

Knapp CM. Engineering siRNA Lipid Nanoparticles for the Treatment of Mantle Cell Lymphoma. [Internet] [Thesis]. Carnegie Mellon University; 2017. [cited 2019 Sep 17]. Available from: http://repository.cmu.edu/dissertations/886.

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

Council of Science Editors:

Knapp CM. Engineering siRNA Lipid Nanoparticles for the Treatment of Mantle Cell Lymphoma. [Thesis]. Carnegie Mellon University; 2017. Available from: http://repository.cmu.edu/dissertations/886

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


University of California – Irvine

23. Zeng, Hanxiang. Rational Design of Synthetic Vectors for siRNA Delivery.

Degree: Chemistry, 2014, University of California – Irvine

 Despite promising potentials for disease treatment, clinical application of RNAi is greatly limited by the lack of safe and effective delivery vectors. In this dissertation,… (more)

Subjects/Keywords: Chemistry; Dendrimer; Gene delivery; Polyamide; siRNA; Synthetic Vector

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APA (6th Edition):

Zeng, H. (2014). Rational Design of Synthetic Vectors for siRNA Delivery. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/64z6f823

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):

Zeng, Hanxiang. “Rational Design of Synthetic Vectors for siRNA Delivery.” 2014. Thesis, University of California – Irvine. Accessed September 17, 2019. http://www.escholarship.org/uc/item/64z6f823.

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

MLA Handbook (7th Edition):

Zeng, Hanxiang. “Rational Design of Synthetic Vectors for siRNA Delivery.” 2014. Web. 17 Sep 2019.

Vancouver:

Zeng H. Rational Design of Synthetic Vectors for siRNA Delivery. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2019 Sep 17]. Available from: http://www.escholarship.org/uc/item/64z6f823.

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

Council of Science Editors:

Zeng H. Rational Design of Synthetic Vectors for siRNA Delivery. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/64z6f823

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


University of California – Berkeley

24. KIERSTEAD, PAUL HENRY. Polymers for Drug Delivery: Extended Circulation and siRNA Transfection.

Degree: Chemistry, 2013, University of California – Berkeley

 Polymers are extensively used in the field of drug delivery for many applications. The ability to tailor the physical and in vivo properties of polymers… (more)

Subjects/Keywords: Chemistry; Dendrimer; Drug Delivery; Extended Circulation; PEG; Polymer; siRNA

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APA (6th Edition):

KIERSTEAD, P. H. (2013). Polymers for Drug Delivery: Extended Circulation and siRNA Transfection. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6111q40t

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):

KIERSTEAD, PAUL HENRY. “Polymers for Drug Delivery: Extended Circulation and siRNA Transfection.” 2013. Thesis, University of California – Berkeley. Accessed September 17, 2019. http://www.escholarship.org/uc/item/6111q40t.

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

MLA Handbook (7th Edition):

KIERSTEAD, PAUL HENRY. “Polymers for Drug Delivery: Extended Circulation and siRNA Transfection.” 2013. Web. 17 Sep 2019.

Vancouver:

KIERSTEAD PH. Polymers for Drug Delivery: Extended Circulation and siRNA Transfection. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2019 Sep 17]. Available from: http://www.escholarship.org/uc/item/6111q40t.

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

Council of Science Editors:

KIERSTEAD PH. Polymers for Drug Delivery: Extended Circulation and siRNA Transfection. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/6111q40t

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

25. Alwani, Saniya. AMINO ACID FUNCTIONALIZED NANODIAMONDS AS GENE DELIVERY VECTORS: SYNTHESIS, PHYSICOCHEMICAL CHARACTERIZATION AND CELLULAR INTERACTION STUDIES.

Degree: 2015, University of Saskatchewan

 Nanodiamonds (NDs) are the most biocompatible member of the carbon nanofamily which are widely researched for diagnostic and therapeutic applications. Unlike other carbon nanomaterials, the… (more)

Subjects/Keywords: nanodiamonds; siRNA delivery

…Colloidal Dispersion for in vitro Cellular Uptake Studies and siRNA Delivery Application ..... 76… …73 4.5.6 Binding of fNDs with pDNA and siRNA… …101 5.6.10 Flow cytometry for lys-ND/siRNA diamoplexes… …Delivery and Expression of Small Interfering RNA and in vitro Toxicity Analysis… …142 10.1.5 Nanodiamonds for Small Molecule Delivery (Section 2.8.4.1)… 

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APA (6th Edition):

Alwani, S. (2015). AMINO ACID FUNCTIONALIZED NANODIAMONDS AS GENE DELIVERY VECTORS: SYNTHESIS, PHYSICOCHEMICAL CHARACTERIZATION AND CELLULAR INTERACTION STUDIES. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2015-09-2219

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):

Alwani, Saniya. “AMINO ACID FUNCTIONALIZED NANODIAMONDS AS GENE DELIVERY VECTORS: SYNTHESIS, PHYSICOCHEMICAL CHARACTERIZATION AND CELLULAR INTERACTION STUDIES.” 2015. Thesis, University of Saskatchewan. Accessed September 17, 2019. http://hdl.handle.net/10388/ETD-2015-09-2219.

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

MLA Handbook (7th Edition):

Alwani, Saniya. “AMINO ACID FUNCTIONALIZED NANODIAMONDS AS GENE DELIVERY VECTORS: SYNTHESIS, PHYSICOCHEMICAL CHARACTERIZATION AND CELLULAR INTERACTION STUDIES.” 2015. Web. 17 Sep 2019.

Vancouver:

Alwani S. AMINO ACID FUNCTIONALIZED NANODIAMONDS AS GENE DELIVERY VECTORS: SYNTHESIS, PHYSICOCHEMICAL CHARACTERIZATION AND CELLULAR INTERACTION STUDIES. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10388/ETD-2015-09-2219.

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

Council of Science Editors:

Alwani S. AMINO ACID FUNCTIONALIZED NANODIAMONDS AS GENE DELIVERY VECTORS: SYNTHESIS, PHYSICOCHEMICAL CHARACTERIZATION AND CELLULAR INTERACTION STUDIES. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/ETD-2015-09-2219

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


University of Waterloo

26. Chen, Baoling. Characterization and evaluation of amphipathic, cationic peptides for small interfering RNA delivery.

Degree: 2015, University of Waterloo

 RNA interference (RNAi) is a highly efficient and specific posttranscriptional gene silencing process, which can be triggered by small interfering RNA. The efficiency and specificity… (more)

Subjects/Keywords: Peptide; siRNA delivery; RNA interference; cytotoxicity; gene silencing

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APA (6th Edition):

Chen, B. (2015). Characterization and evaluation of amphipathic, cationic peptides for small interfering RNA delivery. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/9447

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

Chicago Manual of Style (16th Edition):

Chen, Baoling. “Characterization and evaluation of amphipathic, cationic peptides for small interfering RNA delivery.” 2015. Thesis, University of Waterloo. Accessed September 17, 2019. http://hdl.handle.net/10012/9447.

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

MLA Handbook (7th Edition):

Chen, Baoling. “Characterization and evaluation of amphipathic, cationic peptides for small interfering RNA delivery.” 2015. Web. 17 Sep 2019.

Vancouver:

Chen B. Characterization and evaluation of amphipathic, cationic peptides for small interfering RNA delivery. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10012/9447.

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

Council of Science Editors:

Chen B. Characterization and evaluation of amphipathic, cationic peptides for small interfering RNA delivery. [Thesis]. University of Waterloo; 2015. Available from: http://hdl.handle.net/10012/9447

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


Vanderbilt University

27. Sarett, Samantha Mara. Hydrophobic Modification of siRNA to Improve Delivery and Efficacy of RNAi Therapeutics.

Degree: PhD, Biomedical Engineering, 2017, Vanderbilt University

 Small interfering RNA (siRNA) can potently and specifically suppress translation of any gene, including intracellular targets traditionally considered âundruggableâ. However, emergence of translational siRNA therapies… (more)

Subjects/Keywords: hydrophobic modification; delivery efficacy; pharmacokinetics; gene silencing; siRNA

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APA (6th Edition):

Sarett, S. M. (2017). Hydrophobic Modification of siRNA to Improve Delivery and Efficacy of RNAi Therapeutics. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03272017-155710/ ;

Chicago Manual of Style (16th Edition):

Sarett, Samantha Mara. “Hydrophobic Modification of siRNA to Improve Delivery and Efficacy of RNAi Therapeutics.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed September 17, 2019. http://etd.library.vanderbilt.edu/available/etd-03272017-155710/ ;.

MLA Handbook (7th Edition):

Sarett, Samantha Mara. “Hydrophobic Modification of siRNA to Improve Delivery and Efficacy of RNAi Therapeutics.” 2017. Web. 17 Sep 2019.

Vancouver:

Sarett SM. Hydrophobic Modification of siRNA to Improve Delivery and Efficacy of RNAi Therapeutics. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2019 Sep 17]. Available from: http://etd.library.vanderbilt.edu/available/etd-03272017-155710/ ;.

Council of Science Editors:

Sarett SM. Hydrophobic Modification of siRNA to Improve Delivery and Efficacy of RNAi Therapeutics. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://etd.library.vanderbilt.edu/available/etd-03272017-155710/ ;


University of Waterloo

28. Law, Maggie Man Kei. Peptide Mediated siRNA Delivery: Physicochemical and in vitro Characterizations.

Degree: 2008, University of Waterloo

 Short interfering RNAs (siRNAs) trigger RNA interference (RNAi) both in vitro and in vivo, where the expression of the encoded protein is silenced. Its potential… (more)

Subjects/Keywords: siRNA; complexation; peptide; delivery

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APA (6th Edition):

Law, M. M. K. (2008). Peptide Mediated siRNA Delivery: Physicochemical and in vitro Characterizations. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/3504

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):

Law, Maggie Man Kei. “Peptide Mediated siRNA Delivery: Physicochemical and in vitro Characterizations.” 2008. Thesis, University of Waterloo. Accessed September 17, 2019. http://hdl.handle.net/10012/3504.

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

MLA Handbook (7th Edition):

Law, Maggie Man Kei. “Peptide Mediated siRNA Delivery: Physicochemical and in vitro Characterizations.” 2008. Web. 17 Sep 2019.

Vancouver:

Law MMK. Peptide Mediated siRNA Delivery: Physicochemical and in vitro Characterizations. [Internet] [Thesis]. University of Waterloo; 2008. [cited 2019 Sep 17]. Available from: http://hdl.handle.net/10012/3504.

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

Council of Science Editors:

Law MMK. Peptide Mediated siRNA Delivery: Physicochemical and in vitro Characterizations. [Thesis]. University of Waterloo; 2008. Available from: http://hdl.handle.net/10012/3504

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


University of California – San Francisco

29. Walsh, Colin. Design, Synthesis and Characterization of Novel Zwitterionic Lipids for Drug and siRNA Delivery Applications.

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

 Lipid-based nanoparticles have long been used to deliver biologically active molecules such as drugs, proteins, peptides, DNA, and siRNA in vivo. Liposomes and lipoplexes alter… (more)

Subjects/Keywords: Pharmaceutical sciences; Materials Science; Drug Delivery; Lipid Synthesis; Membrane Biophysics; siRNA

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

APA (6th Edition):

Walsh, C. (2012). Design, Synthesis and Characterization of Novel Zwitterionic Lipids for Drug and siRNA Delivery Applications. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/151167n1

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):

Walsh, Colin. “Design, Synthesis and Characterization of Novel Zwitterionic Lipids for Drug and siRNA Delivery Applications.” 2012. Thesis, University of California – San Francisco. Accessed September 17, 2019. http://www.escholarship.org/uc/item/151167n1.

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

MLA Handbook (7th Edition):

Walsh, Colin. “Design, Synthesis and Characterization of Novel Zwitterionic Lipids for Drug and siRNA Delivery Applications.” 2012. Web. 17 Sep 2019.

Vancouver:

Walsh C. Design, Synthesis and Characterization of Novel Zwitterionic Lipids for Drug and siRNA Delivery Applications. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Sep 17]. Available from: http://www.escholarship.org/uc/item/151167n1.

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

Council of Science Editors:

Walsh C. Design, Synthesis and Characterization of Novel Zwitterionic Lipids for Drug and siRNA Delivery Applications. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/151167n1

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


University of California – San Francisco

30. Tiffany, Matthew. Tracking Fluorescent Liposomes and Fluorescent siRNA Contents During Internalization and Trafficking in Cultured Cells.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2013, University of California – San Francisco

 The large molecular weight, poly-anionic, and labile nature of small interfering RNA (siRNA) necessitate that these macromolecules are associated with carriers for cellular delivery. Lipid-based… (more)

Subjects/Keywords: Pharmaceutical sciences; delivery; endocytosis; lipoplex; liposome; RNAi; siRNA

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

APA (6th Edition):

Tiffany, M. (2013). Tracking Fluorescent Liposomes and Fluorescent siRNA Contents During Internalization and Trafficking in Cultured Cells. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7nv2v78c

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):

Tiffany, Matthew. “Tracking Fluorescent Liposomes and Fluorescent siRNA Contents During Internalization and Trafficking in Cultured Cells.” 2013. Thesis, University of California – San Francisco. Accessed September 17, 2019. http://www.escholarship.org/uc/item/7nv2v78c.

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

MLA Handbook (7th Edition):

Tiffany, Matthew. “Tracking Fluorescent Liposomes and Fluorescent siRNA Contents During Internalization and Trafficking in Cultured Cells.” 2013. Web. 17 Sep 2019.

Vancouver:

Tiffany M. Tracking Fluorescent Liposomes and Fluorescent siRNA Contents During Internalization and Trafficking in Cultured Cells. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2019 Sep 17]. Available from: http://www.escholarship.org/uc/item/7nv2v78c.

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

Council of Science Editors:

Tiffany M. Tracking Fluorescent Liposomes and Fluorescent siRNA Contents During Internalization and Trafficking in Cultured Cells. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/7nv2v78c

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

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