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You searched for subject:(Cell delivery). Showing records 1 – 30 of 219 total matches.

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1. WHYTE, WILLIAM. THEREPI: A therapeutic epicardial reservoir for the treatment of cardiac disease.

Degree: School of Engineering. Discipline of Mechanical & Manuf. Eng, 2019, Trinity College Dublin

 The clinical translation of regenerative therapy for the diseased heart, whether in the form of cells, macromolecules or small molecules, is hampered by several factors:… (more)

Subjects/Keywords: Replenishable cell delivery

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APA (6th Edition):

WHYTE, W. (2019). THEREPI: A therapeutic epicardial reservoir for the treatment of cardiac disease. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/86761

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):

WHYTE, WILLIAM. “THEREPI: A therapeutic epicardial reservoir for the treatment of cardiac disease.” 2019. Thesis, Trinity College Dublin. Accessed November 27, 2020. http://hdl.handle.net/2262/86761.

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

MLA Handbook (7th Edition):

WHYTE, WILLIAM. “THEREPI: A therapeutic epicardial reservoir for the treatment of cardiac disease.” 2019. Web. 27 Nov 2020.

Vancouver:

WHYTE W. THEREPI: A therapeutic epicardial reservoir for the treatment of cardiac disease. [Internet] [Thesis]. Trinity College Dublin; 2019. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2262/86761.

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

Council of Science Editors:

WHYTE W. THEREPI: A therapeutic epicardial reservoir for the treatment of cardiac disease. [Thesis]. Trinity College Dublin; 2019. Available from: http://hdl.handle.net/2262/86761

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


Texas A&M University

2. Erazo, Alfredo. Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms.

Degree: PhD, Biochemistry, 2014, Texas A&M University

Cell-penetrating peptides (CPPs) facilitate the delivery of cell-impermeable macrmolecules across the plasma membrane of live cells. CPPs act as biological Trojan horses by hijacking and… (more)

Subjects/Keywords: protein delivery; cell-penetrating peptides

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APA (6th Edition):

Erazo, A. (2014). Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154025

Chicago Manual of Style (16th Edition):

Erazo, Alfredo. “Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms.” 2014. Doctoral Dissertation, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/154025.

MLA Handbook (7th Edition):

Erazo, Alfredo. “Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms.” 2014. Web. 27 Nov 2020.

Vancouver:

Erazo A. Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/154025.

Council of Science Editors:

Erazo A. Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154025


University of Illinois – Urbana-Champaign

3. Cheng, Felice. Study of drug delivery and cell encapsulation using biocompatible hydrogel.

Degree: PhD, 1200, 2011, University of Illinois – Urbana-Champaign

 Hydrogel particles encapsulating biomolecules or living cells are becoming an attractive means to mediate drug delivery or facilitate cell-based treatment of diseases. These particles are… (more)

Subjects/Keywords: Hydrogel; drug delivery; cell encapsulation

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APA (6th Edition):

Cheng, F. (2011). Study of drug delivery and cell encapsulation using biocompatible hydrogel. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18647

Chicago Manual of Style (16th Edition):

Cheng, Felice. “Study of drug delivery and cell encapsulation using biocompatible hydrogel.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 27, 2020. http://hdl.handle.net/2142/18647.

MLA Handbook (7th Edition):

Cheng, Felice. “Study of drug delivery and cell encapsulation using biocompatible hydrogel.” 2011. Web. 27 Nov 2020.

Vancouver:

Cheng F. Study of drug delivery and cell encapsulation using biocompatible hydrogel. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2142/18647.

Council of Science Editors:

Cheng F. Study of drug delivery and cell encapsulation using biocompatible hydrogel. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18647


University of Toronto

4. Caicco, Matthew. Hyaluronan-methylcellulose Hydrogels for Cell and Drug Delivery to the Injured Central Nervous System.

Degree: 2012, University of Toronto

Spinal cord injury and stroke are two devastating neurological events that lack effective clinical treatments. Recent neuroregenerative approaches involving the delivery of cells or drugs… (more)

Subjects/Keywords: Drug Delivery; Cell Delivery; Hydrogel; Central Nervous System; 0542; 0541

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APA (6th Edition):

Caicco, M. (2012). Hyaluronan-methylcellulose Hydrogels for Cell and Drug Delivery to the Injured Central Nervous System. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33350

Chicago Manual of Style (16th Edition):

Caicco, Matthew. “Hyaluronan-methylcellulose Hydrogels for Cell and Drug Delivery to the Injured Central Nervous System.” 2012. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/33350.

MLA Handbook (7th Edition):

Caicco, Matthew. “Hyaluronan-methylcellulose Hydrogels for Cell and Drug Delivery to the Injured Central Nervous System.” 2012. Web. 27 Nov 2020.

Vancouver:

Caicco M. Hyaluronan-methylcellulose Hydrogels for Cell and Drug Delivery to the Injured Central Nervous System. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/33350.

Council of Science Editors:

Caicco M. Hyaluronan-methylcellulose Hydrogels for Cell and Drug Delivery to the Injured Central Nervous System. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33350


Cornell University

5. Kiatwuthinon, Pichamon. Synthetic Dna Nanomaterials For Drug Delivery And 3D Cell Culture.

Degree: PhD, Agricultural and Biological Engineering, 2013, Cornell University

 Interest in the use of DNA nanotechnology in biomedical applications has increased tremendously in the last decade due to the uniqueness of DNA properties that… (more)

Subjects/Keywords: dna nanomaterials; drug delivery; 3d cell culture

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APA (6th Edition):

Kiatwuthinon, P. (2013). Synthetic Dna Nanomaterials For Drug Delivery And 3D Cell Culture. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34331

Chicago Manual of Style (16th Edition):

Kiatwuthinon, Pichamon. “Synthetic Dna Nanomaterials For Drug Delivery And 3D Cell Culture.” 2013. Doctoral Dissertation, Cornell University. Accessed November 27, 2020. http://hdl.handle.net/1813/34331.

MLA Handbook (7th Edition):

Kiatwuthinon, Pichamon. “Synthetic Dna Nanomaterials For Drug Delivery And 3D Cell Culture.” 2013. Web. 27 Nov 2020.

Vancouver:

Kiatwuthinon P. Synthetic Dna Nanomaterials For Drug Delivery And 3D Cell Culture. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1813/34331.

Council of Science Editors:

Kiatwuthinon P. Synthetic Dna Nanomaterials For Drug Delivery And 3D Cell Culture. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34331


University of Notre Dame

6. Kara Marie Harmatys. Fluorescence Molecular Imaging and Photothermal Therapy Using Small Molecules</h1>.

Degree: Chemistry and Biochemistry, 2015, University of Notre Dame

  Second-generation fluorescent molecular imaging probes were evaluated for their ability to target dead and dying cells. This was accomplished using epi-fluorescence microscopy, whole-body fluorescence… (more)

Subjects/Keywords: cell death; croconaine dyes; drug delivery

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APA (6th Edition):

Harmatys, K. M. (2015). Fluorescence Molecular Imaging and Photothermal Therapy Using Small Molecules</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/m900ns08d68

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):

Harmatys, Kara Marie. “Fluorescence Molecular Imaging and Photothermal Therapy Using Small Molecules</h1>.” 2015. Thesis, University of Notre Dame. Accessed November 27, 2020. https://curate.nd.edu/show/m900ns08d68.

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

MLA Handbook (7th Edition):

Harmatys, Kara Marie. “Fluorescence Molecular Imaging and Photothermal Therapy Using Small Molecules</h1>.” 2015. Web. 27 Nov 2020.

Vancouver:

Harmatys KM. Fluorescence Molecular Imaging and Photothermal Therapy Using Small Molecules</h1>. [Internet] [Thesis]. University of Notre Dame; 2015. [cited 2020 Nov 27]. Available from: https://curate.nd.edu/show/m900ns08d68.

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

Council of Science Editors:

Harmatys KM. Fluorescence Molecular Imaging and Photothermal Therapy Using Small Molecules</h1>. [Thesis]. University of Notre Dame; 2015. Available from: https://curate.nd.edu/show/m900ns08d68

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


University of Waterloo

7. 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 November 27, 2020. 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. 27 Nov 2020.

Vancouver:

Pan R. Stearylated Peptides for Therapeutic siRNA Delivery and Their Cellular Uptake Mechanisms. [Internet] [Thesis]. University of Waterloo; 2015. [cited 2020 Nov 27]. 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


University of New South Wales

8. Kim, Yoseop. Core-Shell drug delivery system for albendazole to treat Ovarian Cancer: From RAFT polymer synthesis to Cellular Uptake.

Degree: Centre for Advanced Macromolecular Design, 2011, University of New South Wales

 The aim of this thesis is to investigate the applicability of polymeric nano-particles synthesized via reversible addition fragmentation chain transfer (RAFT) polymerization that can be… (more)

Subjects/Keywords: Drug delivery; RAFT polymerization; Micelles; Cell uptake

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APA (6th Edition):

Kim, Y. (2011). Core-Shell drug delivery system for albendazole to treat Ovarian Cancer: From RAFT polymer synthesis to Cellular Uptake. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51781 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10448/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Kim, Yoseop. “Core-Shell drug delivery system for albendazole to treat Ovarian Cancer: From RAFT polymer synthesis to Cellular Uptake.” 2011. Doctoral Dissertation, University of New South Wales. Accessed November 27, 2020. http://handle.unsw.edu.au/1959.4/51781 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10448/SOURCE02?view=true.

MLA Handbook (7th Edition):

Kim, Yoseop. “Core-Shell drug delivery system for albendazole to treat Ovarian Cancer: From RAFT polymer synthesis to Cellular Uptake.” 2011. Web. 27 Nov 2020.

Vancouver:

Kim Y. Core-Shell drug delivery system for albendazole to treat Ovarian Cancer: From RAFT polymer synthesis to Cellular Uptake. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2020 Nov 27]. Available from: http://handle.unsw.edu.au/1959.4/51781 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10448/SOURCE02?view=true.

Council of Science Editors:

Kim Y. Core-Shell drug delivery system for albendazole to treat Ovarian Cancer: From RAFT polymer synthesis to Cellular Uptake. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51781 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10448/SOURCE02?view=true


Stellenbosch University

9. Visser, Johan Georg. Development of a transendothelial shuttle by macrophage modification.

Degree: MSc, Physiological Sciences, 2016, Stellenbosch University

ENGLISH ABSTRACT: Background: Targeted stem cell delivery via macrophage modification is a novel and relatively non-invasive therapeutic intervention. Monocytes circulate through the vasculature and infiltrate… (more)

Subjects/Keywords: Macrophages  – Activation; Delivery of stem cell; Stem cell delivery via macrophage modification; UCTD

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APA (6th Edition):

Visser, J. G. (2016). Development of a transendothelial shuttle by macrophage modification. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/101404

Chicago Manual of Style (16th Edition):

Visser, Johan Georg. “Development of a transendothelial shuttle by macrophage modification.” 2016. Masters Thesis, Stellenbosch University. Accessed November 27, 2020. http://hdl.handle.net/10019.1/101404.

MLA Handbook (7th Edition):

Visser, Johan Georg. “Development of a transendothelial shuttle by macrophage modification.” 2016. Web. 27 Nov 2020.

Vancouver:

Visser JG. Development of a transendothelial shuttle by macrophage modification. [Internet] [Masters thesis]. Stellenbosch University; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10019.1/101404.

Council of Science Editors:

Visser JG. Development of a transendothelial shuttle by macrophage modification. [Masters Thesis]. Stellenbosch University; 2016. Available from: http://hdl.handle.net/10019.1/101404


California State University – Sacramento

10. Jyothi, Harsha. Human placenta-derived mesenchymal stromal cell exosome-mimicking nanovesicles for neuroprotection.

Degree: MA, Biological Sciences (Stem Cell, 2019, California State University – Sacramento

 Neurological disorders are devastating and affect the daily activities of millions of people globally. A number of neurological diseases lead to neurodegeneration characterized by irreversible… (more)

Subjects/Keywords: Cell-free therapy; Cell-derived drug delivery system; Artificial exosome

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APA (6th Edition):

Jyothi, H. (2019). Human placenta-derived mesenchymal stromal cell exosome-mimicking nanovesicles for neuroprotection. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/210450

Chicago Manual of Style (16th Edition):

Jyothi, Harsha. “Human placenta-derived mesenchymal stromal cell exosome-mimicking nanovesicles for neuroprotection.” 2019. Masters Thesis, California State University – Sacramento. Accessed November 27, 2020. http://hdl.handle.net/10211.3/210450.

MLA Handbook (7th Edition):

Jyothi, Harsha. “Human placenta-derived mesenchymal stromal cell exosome-mimicking nanovesicles for neuroprotection.” 2019. Web. 27 Nov 2020.

Vancouver:

Jyothi H. Human placenta-derived mesenchymal stromal cell exosome-mimicking nanovesicles for neuroprotection. [Internet] [Masters thesis]. California State University – Sacramento; 2019. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10211.3/210450.

Council of Science Editors:

Jyothi H. Human placenta-derived mesenchymal stromal cell exosome-mimicking nanovesicles for neuroprotection. [Masters Thesis]. California State University – Sacramento; 2019. Available from: http://hdl.handle.net/10211.3/210450


Texas A&M University

11. Wang, Ting-Yi. Membrane Oxidation Governed Direct Plasma Membrane Translocation of Cell-Penetrating Peptides in Live Cells: Mechanisms and Implications.

Degree: PhD, Biochemistry, 2016, Texas A&M University

Cell-penetrating peptides (CPPs) enter cells primarily through escaping from endosomal compartments or directly translocating across the plasma membrane. Due to their capability of permeating into… (more)

Subjects/Keywords: Cell-penetrating peptide (CPP); cell delivery; plasma membrane; cell culture; oxidative stress; oxidized lipids

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APA (6th Edition):

Wang, T. (2016). Membrane Oxidation Governed Direct Plasma Membrane Translocation of Cell-Penetrating Peptides in Live Cells: Mechanisms and Implications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158117

Chicago Manual of Style (16th Edition):

Wang, Ting-Yi. “Membrane Oxidation Governed Direct Plasma Membrane Translocation of Cell-Penetrating Peptides in Live Cells: Mechanisms and Implications.” 2016. Doctoral Dissertation, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/158117.

MLA Handbook (7th Edition):

Wang, Ting-Yi. “Membrane Oxidation Governed Direct Plasma Membrane Translocation of Cell-Penetrating Peptides in Live Cells: Mechanisms and Implications.” 2016. Web. 27 Nov 2020.

Vancouver:

Wang T. Membrane Oxidation Governed Direct Plasma Membrane Translocation of Cell-Penetrating Peptides in Live Cells: Mechanisms and Implications. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/158117.

Council of Science Editors:

Wang T. Membrane Oxidation Governed Direct Plasma Membrane Translocation of Cell-Penetrating Peptides in Live Cells: Mechanisms and Implications. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158117


UCLA

12. Boehnke, Natalie. Degradable Hydrogels and Nanogels for the Delivery of Cells and Therapeutics.

Degree: Chemistry, 2017, UCLA

 Degradable polymeric materials such as hydrogels are extensively utilized as delivery vehicles due to their biocompatibility and tunable properties. Encapsulating therapeutic agents inside hydrogels stabilizes… (more)

Subjects/Keywords: Organic chemistry; Materials Science; Biomaterial; Cell Delivery; Degradable; Hydrogel; Nanogel; Protein Delivery

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APA (6th Edition):

Boehnke, N. (2017). Degradable Hydrogels and Nanogels for the Delivery of Cells and Therapeutics. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1t9969gq

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):

Boehnke, Natalie. “Degradable Hydrogels and Nanogels for the Delivery of Cells and Therapeutics.” 2017. Thesis, UCLA. Accessed November 27, 2020. http://www.escholarship.org/uc/item/1t9969gq.

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

MLA Handbook (7th Edition):

Boehnke, Natalie. “Degradable Hydrogels and Nanogels for the Delivery of Cells and Therapeutics.” 2017. Web. 27 Nov 2020.

Vancouver:

Boehnke N. Degradable Hydrogels and Nanogels for the Delivery of Cells and Therapeutics. [Internet] [Thesis]. UCLA; 2017. [cited 2020 Nov 27]. Available from: http://www.escholarship.org/uc/item/1t9969gq.

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

Council of Science Editors:

Boehnke N. Degradable Hydrogels and Nanogels for the Delivery of Cells and Therapeutics. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/1t9969gq

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


McMaster University

13. Fitzpatrick, Scott D. MINIMALLY INVASIVE COPOLYMERS FOR POSTERIOR SEGMENT OCULAR THERAPEUTICS.

Degree: PhD, 2012, McMaster University

Efficient delivery of therapeutic cell and pharmaceutical suspensions to the posterior segment of the eye remains an elusive goal. Delivery is made difficult by… (more)

Subjects/Keywords: Ophthalmic materials; biomaterials; N-isopropylacrylamide; PNIPAAm; drug delivery; cell delivery; Biomaterials; Biomaterials

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APA (6th Edition):

Fitzpatrick, S. D. (2012). MINIMALLY INVASIVE COPOLYMERS FOR POSTERIOR SEGMENT OCULAR THERAPEUTICS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12080

Chicago Manual of Style (16th Edition):

Fitzpatrick, Scott D. “MINIMALLY INVASIVE COPOLYMERS FOR POSTERIOR SEGMENT OCULAR THERAPEUTICS.” 2012. Doctoral Dissertation, McMaster University. Accessed November 27, 2020. http://hdl.handle.net/11375/12080.

MLA Handbook (7th Edition):

Fitzpatrick, Scott D. “MINIMALLY INVASIVE COPOLYMERS FOR POSTERIOR SEGMENT OCULAR THERAPEUTICS.” 2012. Web. 27 Nov 2020.

Vancouver:

Fitzpatrick SD. MINIMALLY INVASIVE COPOLYMERS FOR POSTERIOR SEGMENT OCULAR THERAPEUTICS. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/11375/12080.

Council of Science Editors:

Fitzpatrick SD. MINIMALLY INVASIVE COPOLYMERS FOR POSTERIOR SEGMENT OCULAR THERAPEUTICS. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12080


University of Southern California

14. Kuwahara, Kenrick. Enzymatically crosslinked scaffold with controllable cell and growth factor delivery for use in tissue engineering.

Degree: PhD, Biomedical Engineering, 2011, University of Southern California

 Tissue engineering is a multidisciplinary field that applies the principles of biology and engineering to restore, improve, or maintain functions of tissue or organs. Damaged… (more)

Subjects/Keywords: gelatin; transglutaminase; tissue engineering; cell delivery; growth factor delivery; BMP-2; mesenchymal stem cells

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APA (6th Edition):

Kuwahara, K. (2011). Enzymatically crosslinked scaffold with controllable cell and growth factor delivery for use in tissue engineering. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/461989/rec/2410

Chicago Manual of Style (16th Edition):

Kuwahara, Kenrick. “Enzymatically crosslinked scaffold with controllable cell and growth factor delivery for use in tissue engineering.” 2011. Doctoral Dissertation, University of Southern California. Accessed November 27, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/461989/rec/2410.

MLA Handbook (7th Edition):

Kuwahara, Kenrick. “Enzymatically crosslinked scaffold with controllable cell and growth factor delivery for use in tissue engineering.” 2011. Web. 27 Nov 2020.

Vancouver:

Kuwahara K. Enzymatically crosslinked scaffold with controllable cell and growth factor delivery for use in tissue engineering. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Nov 27]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/461989/rec/2410.

Council of Science Editors:

Kuwahara K. Enzymatically crosslinked scaffold with controllable cell and growth factor delivery for use in tissue engineering. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/461989/rec/2410


Georgia Tech

15. Liu, Ying. The impact of physical and biological factors on intracellular uptake, trafficking and gene transfection after ultrasound exposure.

Degree: PhD, Chemical Engineering, 2011, Georgia Tech

 We used megahertz pulsed ultrasound and studied gene transfection with a human prostate cancer cell line. We first studied the compromise of cell viability and… (more)

Subjects/Keywords: Drug delivery; Gene therapy; Gene transfection; Ultrasound; Drug delivery systems; Ultrasonics in medicine; Cell death

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

APA (6th Edition):

Liu, Y. (2011). The impact of physical and biological factors on intracellular uptake, trafficking and gene transfection after ultrasound exposure. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/43626

Chicago Manual of Style (16th Edition):

Liu, Ying. “The impact of physical and biological factors on intracellular uptake, trafficking and gene transfection after ultrasound exposure.” 2011. Doctoral Dissertation, Georgia Tech. Accessed November 27, 2020. http://hdl.handle.net/1853/43626.

MLA Handbook (7th Edition):

Liu, Ying. “The impact of physical and biological factors on intracellular uptake, trafficking and gene transfection after ultrasound exposure.” 2011. Web. 27 Nov 2020.

Vancouver:

Liu Y. The impact of physical and biological factors on intracellular uptake, trafficking and gene transfection after ultrasound exposure. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1853/43626.

Council of Science Editors:

Liu Y. The impact of physical and biological factors on intracellular uptake, trafficking and gene transfection after ultrasound exposure. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/43626

16. HUANG, PO-JU. From Nano to Micro: Versatile Strategies for Near-Infrared Light-controlled Nitric Oxide Delivery and Their Therapeutic Applications.

Degree: 2017, University of California – eScholarship, University of California

 Nitric oxide (NO) has attracted considerable attention due to its promising applications in cancer treatment. The therapeutic effect of NO pro-drugs greatly depends on the… (more)

Subjects/Keywords: Inorganic chemistry; Bioengineering; Materials Science; cell-meidated micro-delivery; Nitric oxide; peptide modified nano-delivery; photochemical drug delivery

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APA (6th Edition):

HUANG, P. (2017). From Nano to Micro: Versatile Strategies for Near-Infrared Light-controlled Nitric Oxide Delivery and Their Therapeutic Applications. (Thesis). University of California – eScholarship, University of California. Retrieved from http://www.escholarship.org/uc/item/61c2210j

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):

HUANG, PO-JU. “From Nano to Micro: Versatile Strategies for Near-Infrared Light-controlled Nitric Oxide Delivery and Their Therapeutic Applications.” 2017. Thesis, University of California – eScholarship, University of California. Accessed November 27, 2020. http://www.escholarship.org/uc/item/61c2210j.

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

MLA Handbook (7th Edition):

HUANG, PO-JU. “From Nano to Micro: Versatile Strategies for Near-Infrared Light-controlled Nitric Oxide Delivery and Their Therapeutic Applications.” 2017. Web. 27 Nov 2020.

Vancouver:

HUANG P. From Nano to Micro: Versatile Strategies for Near-Infrared Light-controlled Nitric Oxide Delivery and Their Therapeutic Applications. [Internet] [Thesis]. University of California – eScholarship, University of California; 2017. [cited 2020 Nov 27]. Available from: http://www.escholarship.org/uc/item/61c2210j.

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

Council of Science Editors:

HUANG P. From Nano to Micro: Versatile Strategies for Near-Infrared Light-controlled Nitric Oxide Delivery and Their Therapeutic Applications. [Thesis]. University of California – eScholarship, University of California; 2017. Available from: http://www.escholarship.org/uc/item/61c2210j

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


The Ohio State University

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

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 27, 2020. 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. 27 Nov 2020.

Vancouver:

Qian Z. Developments and Applications of Cyclic Cell Penetrating Peptides. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Nov 27]. 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


University of California – Berkeley

18. Downing, Timothy. Biomaterials for Cell Engineering and Regenerative Medicine.

Degree: Bioengineering, 2013, University of California – Berkeley

 The promise of regenerative medicine relies on the ability to tightly control cell behavior. Given the broad influence of epigenetics in cell behavior and phenotype… (more)

Subjects/Keywords: Biomedical engineering; Biomechanics; Drug-delivery; Epigenetics; iPS cell reprogramming; Nanomaterials; Stem cell therapy

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APA (6th Edition):

Downing, T. (2013). Biomaterials for Cell Engineering and Regenerative Medicine. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/13m6r4sr

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):

Downing, Timothy. “Biomaterials for Cell Engineering and Regenerative Medicine.” 2013. Thesis, University of California – Berkeley. Accessed November 27, 2020. http://www.escholarship.org/uc/item/13m6r4sr.

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

MLA Handbook (7th Edition):

Downing, Timothy. “Biomaterials for Cell Engineering and Regenerative Medicine.” 2013. Web. 27 Nov 2020.

Vancouver:

Downing T. Biomaterials for Cell Engineering and Regenerative Medicine. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Nov 27]. Available from: http://www.escholarship.org/uc/item/13m6r4sr.

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

Council of Science Editors:

Downing T. Biomaterials for Cell Engineering and Regenerative Medicine. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/13m6r4sr

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


UCLA

19. Wu, Yi-Chien. Massively Parallel Delivery of Large-sized Cargo into Mammalian Cells with Light Pulses.

Degree: Mechanical Engineering, 2014, UCLA

 Enabling technologies that transfer micron-sized objects into mammalian cells are needed to advance key applications in cell engineering. High-throughput delivery of organelles, modified intracellular pathogens,… (more)

Subjects/Keywords: Biomedical engineering; Engineering; Mechanical engineering; Cell engineering; Cell surgery; Large cargo delivery

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APA (6th Edition):

Wu, Y. (2014). Massively Parallel Delivery of Large-sized Cargo into Mammalian Cells with Light Pulses. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/2zx6b8kf

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):

Wu, Yi-Chien. “Massively Parallel Delivery of Large-sized Cargo into Mammalian Cells with Light Pulses.” 2014. Thesis, UCLA. Accessed November 27, 2020. http://www.escholarship.org/uc/item/2zx6b8kf.

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

MLA Handbook (7th Edition):

Wu, Yi-Chien. “Massively Parallel Delivery of Large-sized Cargo into Mammalian Cells with Light Pulses.” 2014. Web. 27 Nov 2020.

Vancouver:

Wu Y. Massively Parallel Delivery of Large-sized Cargo into Mammalian Cells with Light Pulses. [Internet] [Thesis]. UCLA; 2014. [cited 2020 Nov 27]. Available from: http://www.escholarship.org/uc/item/2zx6b8kf.

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

Council of Science Editors:

Wu Y. Massively Parallel Delivery of Large-sized Cargo into Mammalian Cells with Light Pulses. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/2zx6b8kf

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


University of Michigan

20. Zhang, Zhanpeng. Advanced Microspheres as Injectable Cell Carriers for Tissue Engineering.

Degree: PhD, Biomedical Engineering, 2015, University of Michigan

 Biodegradable polymer microspheres have emerged as injectable cell carriers for the regeneration and repair of irregularly-shaped tissue defects. The physical structure and chemical composition of… (more)

Subjects/Keywords: tissue regeneration; cell carrier; stem cell; polymer self-assembly; biomimetic; drug delivery; Biomedical Engineering; Engineering

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APA (6th Edition):

Zhang, Z. (2015). Advanced Microspheres as Injectable Cell Carriers for Tissue Engineering. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111559

Chicago Manual of Style (16th Edition):

Zhang, Zhanpeng. “Advanced Microspheres as Injectable Cell Carriers for Tissue Engineering.” 2015. Doctoral Dissertation, University of Michigan. Accessed November 27, 2020. http://hdl.handle.net/2027.42/111559.

MLA Handbook (7th Edition):

Zhang, Zhanpeng. “Advanced Microspheres as Injectable Cell Carriers for Tissue Engineering.” 2015. Web. 27 Nov 2020.

Vancouver:

Zhang Z. Advanced Microspheres as Injectable Cell Carriers for Tissue Engineering. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2027.42/111559.

Council of Science Editors:

Zhang Z. Advanced Microspheres as Injectable Cell Carriers for Tissue Engineering. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111559


Georgia Tech

21. Headen, Devon M. Microfluidics-based microgel synthesis for immunoisolation and immunomodulation in pancreatic islet transplantation.

Degree: PhD, Mechanical Engineering, 2017, Georgia Tech

 Encapsulation of islets in hydrogel microspheres (microgels) before transplantation into diabetic recipients can establish an adequate immuno-isolation barrier to mitigate allogeneic rejection. The synthetic hydrogel… (more)

Subjects/Keywords: Microfluidics; Cell encapsulation; Microencapsulation; Protein delivery; Pancreatic islet; Mesenchymal stem cell; Biomaterials

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APA (6th Edition):

Headen, D. M. (2017). Microfluidics-based microgel synthesis for immunoisolation and immunomodulation in pancreatic islet transplantation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59763

Chicago Manual of Style (16th Edition):

Headen, Devon M. “Microfluidics-based microgel synthesis for immunoisolation and immunomodulation in pancreatic islet transplantation.” 2017. Doctoral Dissertation, Georgia Tech. Accessed November 27, 2020. http://hdl.handle.net/1853/59763.

MLA Handbook (7th Edition):

Headen, Devon M. “Microfluidics-based microgel synthesis for immunoisolation and immunomodulation in pancreatic islet transplantation.” 2017. Web. 27 Nov 2020.

Vancouver:

Headen DM. Microfluidics-based microgel synthesis for immunoisolation and immunomodulation in pancreatic islet transplantation. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1853/59763.

Council of Science Editors:

Headen DM. Microfluidics-based microgel synthesis for immunoisolation and immunomodulation in pancreatic islet transplantation. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/59763


Texas A&M University

22. Muthukrishnan, Nandhini. Intracellular Delivery Using Fluorophore-CPP Conjugates and Light: Mechanisms and Implications.

Degree: PhD, Biochemistry, 2014, Texas A&M University

Cell-penetrating peptides (CPPs) can induce translocation of conjugated macromolecules across the plasma membrane of live cells. The major route of uptake of these CPPs by… (more)

Subjects/Keywords: cell-penetrating peptide; TAT peptide; photochemical internalization; intracellular delivery

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APA (6th Edition):

Muthukrishnan, N. (2014). Intracellular Delivery Using Fluorophore-CPP Conjugates and Light: Mechanisms and Implications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152737

Chicago Manual of Style (16th Edition):

Muthukrishnan, Nandhini. “Intracellular Delivery Using Fluorophore-CPP Conjugates and Light: Mechanisms and Implications.” 2014. Doctoral Dissertation, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/152737.

MLA Handbook (7th Edition):

Muthukrishnan, Nandhini. “Intracellular Delivery Using Fluorophore-CPP Conjugates and Light: Mechanisms and Implications.” 2014. Web. 27 Nov 2020.

Vancouver:

Muthukrishnan N. Intracellular Delivery Using Fluorophore-CPP Conjugates and Light: Mechanisms and Implications. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/152737.

Council of Science Editors:

Muthukrishnan N. Intracellular Delivery Using Fluorophore-CPP Conjugates and Light: Mechanisms and Implications. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152737


UCLA

23. Wattanatorn, Natcha. Nanosphere Lithography for Intracellular Delivery.

Degree: Chemistry, 2019, UCLA

 Nanosphere lithography (NSL) is a simple, high-throughput technique that can be used to form large-area, close-packed monolayer arrays of nanospheres. These arrays can be directly… (more)

Subjects/Keywords: Chemistry; Biomedical engineering; CAR T Cell; gene delivery; nanosphere lithography

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APA (6th Edition):

Wattanatorn, N. (2019). Nanosphere Lithography for Intracellular Delivery. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/7ct205z6

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):

Wattanatorn, Natcha. “Nanosphere Lithography for Intracellular Delivery.” 2019. Thesis, UCLA. Accessed November 27, 2020. http://www.escholarship.org/uc/item/7ct205z6.

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

MLA Handbook (7th Edition):

Wattanatorn, Natcha. “Nanosphere Lithography for Intracellular Delivery.” 2019. Web. 27 Nov 2020.

Vancouver:

Wattanatorn N. Nanosphere Lithography for Intracellular Delivery. [Internet] [Thesis]. UCLA; 2019. [cited 2020 Nov 27]. Available from: http://www.escholarship.org/uc/item/7ct205z6.

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

Council of Science Editors:

Wattanatorn N. Nanosphere Lithography for Intracellular Delivery. [Thesis]. UCLA; 2019. Available from: http://www.escholarship.org/uc/item/7ct205z6

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


University of Toronto

24. Guo, Melinda. Functionalization of Cellulose Nanocrystals with PEG-metal-chelating Diblock Copolymers via Controlled Conjugation in Aqueous Medium.

Degree: 2016, University of Toronto

The surface of cellulose nanocrystals (CNCs) was successfully functionalized with metal chelating diblock copolymers via HyNic-4FB conjugation. Two types of PEG-metal-chelating block polymers with hydrazinonicotinate… (more)

Subjects/Keywords: Cell imaging; Cellulose nanocrystals; Drug delivery; Nanomedicine; 0485

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APA (6th Edition):

Guo, M. (2016). Functionalization of Cellulose Nanocrystals with PEG-metal-chelating Diblock Copolymers via Controlled Conjugation in Aqueous Medium. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/71669

Chicago Manual of Style (16th Edition):

Guo, Melinda. “Functionalization of Cellulose Nanocrystals with PEG-metal-chelating Diblock Copolymers via Controlled Conjugation in Aqueous Medium.” 2016. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/71669.

MLA Handbook (7th Edition):

Guo, Melinda. “Functionalization of Cellulose Nanocrystals with PEG-metal-chelating Diblock Copolymers via Controlled Conjugation in Aqueous Medium.” 2016. Web. 27 Nov 2020.

Vancouver:

Guo M. Functionalization of Cellulose Nanocrystals with PEG-metal-chelating Diblock Copolymers via Controlled Conjugation in Aqueous Medium. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/71669.

Council of Science Editors:

Guo M. Functionalization of Cellulose Nanocrystals with PEG-metal-chelating Diblock Copolymers via Controlled Conjugation in Aqueous Medium. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/71669


University of Toronto

25. Moghaddam, Bahar. Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions.

Degree: 2011, University of Toronto

Conjugation of the Human Immunodeficiency Virus Transactivator of Transcription (TAT) to active proteins allows transport into the intracellular environment. This feature can be harnessed to… (more)

Subjects/Keywords: Cell Penetrating Peptides; Induced pluripotent stem cells; Transcription Factor Delivery; 0541

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APA (6th Edition):

Moghaddam, B. (2011). Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31344

Chicago Manual of Style (16th Edition):

Moghaddam, Bahar. “Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions.” 2011. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/31344.

MLA Handbook (7th Edition):

Moghaddam, Bahar. “Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions.” 2011. Web. 27 Nov 2020.

Vancouver:

Moghaddam B. Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/31344.

Council of Science Editors:

Moghaddam B. Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31344


Australian National University

26. Wang, Yi. Functionalised self-assembled peptide hydrogel for cell transplantation .

Degree: 2018, Australian National University

Cell transplantation has provided a novel approach for the treatment of brain disorders due to its inherent ability to introduce replacement cells for tissue regeneration.… (more)

Subjects/Keywords: self-assembled peptide; hydrogel; drug delivery; cell transplantation; tissue engineering

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APA (6th Edition):

Wang, Y. (2018). Functionalised self-assembled peptide hydrogel for cell transplantation . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/160784

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):

Wang, Yi. “Functionalised self-assembled peptide hydrogel for cell transplantation .” 2018. Thesis, Australian National University. Accessed November 27, 2020. http://hdl.handle.net/1885/160784.

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

MLA Handbook (7th Edition):

Wang, Yi. “Functionalised self-assembled peptide hydrogel for cell transplantation .” 2018. Web. 27 Nov 2020.

Vancouver:

Wang Y. Functionalised self-assembled peptide hydrogel for cell transplantation . [Internet] [Thesis]. Australian National University; 2018. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1885/160784.

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

Council of Science Editors:

Wang Y. Functionalised self-assembled peptide hydrogel for cell transplantation . [Thesis]. Australian National University; 2018. Available from: http://hdl.handle.net/1885/160784

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

27. 임, 선우. Studies on the efficient intracellular delivery vehicle using variable region domain of a cell-penetrating anti-DNA monoclonal antibody.

Degree: 2016, Ajou University

The cell-penetrating antibodies and antibody fragments can be utilized as a tool for the medical diagnosis and treatment. In this study, we have produced the… (more)

Subjects/Keywords: Cell-penetrating antibody; Single domain antibody; Cellular delivery vehicle

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APA (6th Edition):

임, . (2016). Studies on the efficient intracellular delivery vehicle using variable region domain of a cell-penetrating anti-DNA monoclonal antibody. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/13030 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000023101

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):

임, 선우. “Studies on the efficient intracellular delivery vehicle using variable region domain of a cell-penetrating anti-DNA monoclonal antibody.” 2016. Thesis, Ajou University. Accessed November 27, 2020. http://repository.ajou.ac.kr/handle/201003/13030 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000023101.

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

MLA Handbook (7th Edition):

임, 선우. “Studies on the efficient intracellular delivery vehicle using variable region domain of a cell-penetrating anti-DNA monoclonal antibody.” 2016. Web. 27 Nov 2020.

Vancouver:

임 . Studies on the efficient intracellular delivery vehicle using variable region domain of a cell-penetrating anti-DNA monoclonal antibody. [Internet] [Thesis]. Ajou University; 2016. [cited 2020 Nov 27]. Available from: http://repository.ajou.ac.kr/handle/201003/13030 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000023101.

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

Council of Science Editors:

임 . Studies on the efficient intracellular delivery vehicle using variable region domain of a cell-penetrating anti-DNA monoclonal antibody. [Thesis]. Ajou University; 2016. Available from: http://repository.ajou.ac.kr/handle/201003/13030 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000023101

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


Northeastern University

28. Kosovrasti, Verbena Y. Hyaluronic-acid based nanocarriers for RNAi therapy of advanced sepsis.

Degree: PhD, School of Pharmacy, 2015, Northeastern University

 Ever since the first representation of RNAi phenomenon in 1998, its ride has been quite complicated. If handled carefully, RNAi could have the potential of… (more)

Subjects/Keywords: cell delivery; cytokine; hyaluronic acid; inflammation; sepsis; siRNA

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APA (6th Edition):

Kosovrasti, V. Y. (2015). Hyaluronic-acid based nanocarriers for RNAi therapy of advanced sepsis. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20197272

Chicago Manual of Style (16th Edition):

Kosovrasti, Verbena Y. “Hyaluronic-acid based nanocarriers for RNAi therapy of advanced sepsis.” 2015. Doctoral Dissertation, Northeastern University. Accessed November 27, 2020. http://hdl.handle.net/2047/D20197272.

MLA Handbook (7th Edition):

Kosovrasti, Verbena Y. “Hyaluronic-acid based nanocarriers for RNAi therapy of advanced sepsis.” 2015. Web. 27 Nov 2020.

Vancouver:

Kosovrasti VY. Hyaluronic-acid based nanocarriers for RNAi therapy of advanced sepsis. [Internet] [Doctoral dissertation]. Northeastern University; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2047/D20197272.

Council of Science Editors:

Kosovrasti VY. Hyaluronic-acid based nanocarriers for RNAi therapy of advanced sepsis. [Doctoral Dissertation]. Northeastern University; 2015. Available from: http://hdl.handle.net/2047/D20197272


Colorado State University

29. Bruce, Virginia Jane. Protein based technologies to identify, study, and control intracellular processes.

Degree: PhD, Chemistry, 2017, Colorado State University

 Proteins are increasingly used as basic research tools and therapeutics. Their large size, complex structure, and functional group diversity, by virtue of amino acids, often… (more)

Subjects/Keywords: cellular delivery; proteins; cell penetrating peptides; resurfacing; protein engineering

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APA (6th Edition):

Bruce, V. J. (2017). Protein based technologies to identify, study, and control intracellular processes. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/183950

Chicago Manual of Style (16th Edition):

Bruce, Virginia Jane. “Protein based technologies to identify, study, and control intracellular processes.” 2017. Doctoral Dissertation, Colorado State University. Accessed November 27, 2020. http://hdl.handle.net/10217/183950.

MLA Handbook (7th Edition):

Bruce, Virginia Jane. “Protein based technologies to identify, study, and control intracellular processes.” 2017. Web. 27 Nov 2020.

Vancouver:

Bruce VJ. Protein based technologies to identify, study, and control intracellular processes. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10217/183950.

Council of Science Editors:

Bruce VJ. Protein based technologies to identify, study, and control intracellular processes. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/183950


North-West University

30. Burger, Cornel. Formulation, in vitro release and transdermal diffusion of pravastatin by the implementation of the delivery gap principle / Cornel Burger .

Degree: 2014, North-West University

 Active pharmaceutical ingredients (APIs), which are incorporated in different formulations, i.e. creams, gels, foams, etc., are applied to the skin for a therapeutic effect. This… (more)

Subjects/Keywords: Pravastatin; Wiechers; Franz cell; Diffusion studies; Polarity formulations; Delivery Gap Principle

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

APA (6th Edition):

Burger, C. (2014). Formulation, in vitro release and transdermal diffusion of pravastatin by the implementation of the delivery gap principle / Cornel Burger . (Thesis). North-West University. Retrieved from http://hdl.handle.net/10394/14221

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):

Burger, Cornel. “Formulation, in vitro release and transdermal diffusion of pravastatin by the implementation of the delivery gap principle / Cornel Burger .” 2014. Thesis, North-West University. Accessed November 27, 2020. http://hdl.handle.net/10394/14221.

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

MLA Handbook (7th Edition):

Burger, Cornel. “Formulation, in vitro release and transdermal diffusion of pravastatin by the implementation of the delivery gap principle / Cornel Burger .” 2014. Web. 27 Nov 2020.

Vancouver:

Burger C. Formulation, in vitro release and transdermal diffusion of pravastatin by the implementation of the delivery gap principle / Cornel Burger . [Internet] [Thesis]. North-West University; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10394/14221.

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

Council of Science Editors:

Burger C. Formulation, in vitro release and transdermal diffusion of pravastatin by the implementation of the delivery gap principle / Cornel Burger . [Thesis]. North-West University; 2014. Available from: http://hdl.handle.net/10394/14221

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

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