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You searched for subject:(gene therapy). Showing records 1 – 30 of 1177 total matches.

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University of Oxford

1. Antepowicz, Agata. Development of lung and muscle factories to deliver therapeutic monoclonal antibodies.

Degree: PhD, 2018, University of Oxford

 Monoclonal antibodies (mAbs), which represent the largest market of any protein therapeutic, are used in the treatment of conditions such as cancer and autoimmune diseases,… (more)

Subjects/Keywords: Gene therapy

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APA (6th Edition):

Antepowicz, A. (2018). Development of lung and muscle factories to deliver therapeutic monoclonal antibodies. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:0bffd69b-6324-4edf-af7a-c5344cc70359 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780516

Chicago Manual of Style (16th Edition):

Antepowicz, Agata. “Development of lung and muscle factories to deliver therapeutic monoclonal antibodies.” 2018. Doctoral Dissertation, University of Oxford. Accessed September 26, 2020. http://ora.ox.ac.uk/objects/uuid:0bffd69b-6324-4edf-af7a-c5344cc70359 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780516.

MLA Handbook (7th Edition):

Antepowicz, Agata. “Development of lung and muscle factories to deliver therapeutic monoclonal antibodies.” 2018. Web. 26 Sep 2020.

Vancouver:

Antepowicz A. Development of lung and muscle factories to deliver therapeutic monoclonal antibodies. [Internet] [Doctoral dissertation]. University of Oxford; 2018. [cited 2020 Sep 26]. Available from: http://ora.ox.ac.uk/objects/uuid:0bffd69b-6324-4edf-af7a-c5344cc70359 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780516.

Council of Science Editors:

Antepowicz A. Development of lung and muscle factories to deliver therapeutic monoclonal antibodies. [Doctoral Dissertation]. University of Oxford; 2018. Available from: http://ora.ox.ac.uk/objects/uuid:0bffd69b-6324-4edf-af7a-c5344cc70359 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780516


University of Hawaii – Manoa

2. Anderson, Cynthia Dawn. Nonviral vector strategies for ultrasound targeted microbubble destruction-mediated hepatic gene therapy.

Degree: 2015, University of Hawaii – Manoa

Ph.D. University of Hawaii at Manoa 2014.

The goal of this research was to identify an improved delivery system and vectors for noninvasive gene therapy(more)

Subjects/Keywords: gene; therapy

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APA (6th Edition):

Anderson, C. D. (2015). Nonviral vector strategies for ultrasound targeted microbubble destruction-mediated hepatic gene therapy. (Thesis). University of Hawaii – Manoa. Retrieved from http://hdl.handle.net/10125/100285

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):

Anderson, Cynthia Dawn. “Nonviral vector strategies for ultrasound targeted microbubble destruction-mediated hepatic gene therapy.” 2015. Thesis, University of Hawaii – Manoa. Accessed September 26, 2020. http://hdl.handle.net/10125/100285.

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

MLA Handbook (7th Edition):

Anderson, Cynthia Dawn. “Nonviral vector strategies for ultrasound targeted microbubble destruction-mediated hepatic gene therapy.” 2015. Web. 26 Sep 2020.

Vancouver:

Anderson CD. Nonviral vector strategies for ultrasound targeted microbubble destruction-mediated hepatic gene therapy. [Internet] [Thesis]. University of Hawaii – Manoa; 2015. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10125/100285.

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

Council of Science Editors:

Anderson CD. Nonviral vector strategies for ultrasound targeted microbubble destruction-mediated hepatic gene therapy. [Thesis]. University of Hawaii – Manoa; 2015. Available from: http://hdl.handle.net/10125/100285

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


University of Texas Southwestern Medical Center

3. Ellis, Brian Lee. Improving Viral Vectors for Gene Targeting in Gene Therapy.

Degree: 2011, University of Texas Southwestern Medical Center

 Over 10,000 monogenic diseases in the world affect one out of every hundred live births (WHO). Gene targeting is a term that is used describe… (more)

Subjects/Keywords: Gene Targeting; Gene Therapy; Lentivirus

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APA (6th Edition):

Ellis, B. L. (2011). Improving Viral Vectors for Gene Targeting in Gene Therapy. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/837

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):

Ellis, Brian Lee. “Improving Viral Vectors for Gene Targeting in Gene Therapy.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed September 26, 2020. http://hdl.handle.net/2152.5/837.

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

MLA Handbook (7th Edition):

Ellis, Brian Lee. “Improving Viral Vectors for Gene Targeting in Gene Therapy.” 2011. Web. 26 Sep 2020.

Vancouver:

Ellis BL. Improving Viral Vectors for Gene Targeting in Gene Therapy. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2152.5/837.

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

Council of Science Editors:

Ellis BL. Improving Viral Vectors for Gene Targeting in Gene Therapy. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/837

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


Rutgers University

4. FENG, XING, 1987-. Roles of SETD4 in radiation sensitivity and tumorigenesis.

Degree: PhD, Pharmacology, Cellular and Molecular, 2018, Rutgers University

The SET domain protein methyltransferases play a critical role in histone modifications and global epigenetic regulations. Recent evidence suggests that some SET domain proteins may… (more)

Subjects/Keywords: Cancer – Gene therapy

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APA (6th Edition):

FENG, XING, 1. (2018). Roles of SETD4 in radiation sensitivity and tumorigenesis. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/59084/

Chicago Manual of Style (16th Edition):

FENG, XING, 1987-. “Roles of SETD4 in radiation sensitivity and tumorigenesis.” 2018. Doctoral Dissertation, Rutgers University. Accessed September 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/59084/.

MLA Handbook (7th Edition):

FENG, XING, 1987-. “Roles of SETD4 in radiation sensitivity and tumorigenesis.” 2018. Web. 26 Sep 2020.

Vancouver:

FENG, XING 1. Roles of SETD4 in radiation sensitivity and tumorigenesis. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2020 Sep 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59084/.

Council of Science Editors:

FENG, XING 1. Roles of SETD4 in radiation sensitivity and tumorigenesis. [Doctoral Dissertation]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59084/


University of Texas Southwestern Medical Center

5. Checketts, Joshua Allen. Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells.

Degree: 2013, University of Texas Southwestern Medical Center

Gene therapy is the ability to correct diseases at the DNA level and has long been a goal of science and medicine. The earliest gene(more)

Subjects/Keywords: Gene Therapy; Gene Targeting; Severe Combined Immunodeficiency

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APA (6th Edition):

Checketts, J. A. (2013). Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1727

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):

Checketts, Joshua Allen. “Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed September 26, 2020. http://hdl.handle.net/2152.5/1727.

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

MLA Handbook (7th Edition):

Checketts, Joshua Allen. “Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells.” 2013. Web. 26 Sep 2020.

Vancouver:

Checketts JA. Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2152.5/1727.

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

Council of Science Editors:

Checketts JA. Nuclease-Mediated Targeted Gene Insertion at the Adenosine Deaminase Locus in Primary Cells. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1727

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


University of Rochester

6. Badding, Melissa. Cytoplasmic Factors that Impact Intracellular Plasmid Trafficking During Gene Transfer.

Degree: PhD, 2012, University of Rochester

 For non-viral gene transfer to be successful, plasmids must cross several barriers. Very little is known about how plasmids overcome the barrier presented by the… (more)

Subjects/Keywords: Gene Therapy; Trafficking; Nuclear Import

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APA (6th Edition):

Badding, M. (2012). Cytoplasmic Factors that Impact Intracellular Plasmid Trafficking During Gene Transfer. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/25532

Chicago Manual of Style (16th Edition):

Badding, Melissa. “Cytoplasmic Factors that Impact Intracellular Plasmid Trafficking During Gene Transfer.” 2012. Doctoral Dissertation, University of Rochester. Accessed September 26, 2020. http://hdl.handle.net/1802/25532.

MLA Handbook (7th Edition):

Badding, Melissa. “Cytoplasmic Factors that Impact Intracellular Plasmid Trafficking During Gene Transfer.” 2012. Web. 26 Sep 2020.

Vancouver:

Badding M. Cytoplasmic Factors that Impact Intracellular Plasmid Trafficking During Gene Transfer. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1802/25532.

Council of Science Editors:

Badding M. Cytoplasmic Factors that Impact Intracellular Plasmid Trafficking During Gene Transfer. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/25532


University of Toronto

7. Berinstein, Elliot. The Development Of A Novel Chimeric Antigen Receptor Specific For Syndecan-1.

Degree: 2016, University of Toronto

The adoptive transfer of T lymphocytes expressing chimeric antigen receptors (CARs) has become a promising treatment for various cancers. CARs have been shown to redirect… (more)

Subjects/Keywords: Cancer; Gene Therapy; Immunotherapy; 0992

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APA (6th Edition):

Berinstein, E. (2016). The Development Of A Novel Chimeric Antigen Receptor Specific For Syndecan-1. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/90143

Chicago Manual of Style (16th Edition):

Berinstein, Elliot. “The Development Of A Novel Chimeric Antigen Receptor Specific For Syndecan-1.” 2016. Masters Thesis, University of Toronto. Accessed September 26, 2020. http://hdl.handle.net/1807/90143.

MLA Handbook (7th Edition):

Berinstein, Elliot. “The Development Of A Novel Chimeric Antigen Receptor Specific For Syndecan-1.” 2016. Web. 26 Sep 2020.

Vancouver:

Berinstein E. The Development Of A Novel Chimeric Antigen Receptor Specific For Syndecan-1. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1807/90143.

Council of Science Editors:

Berinstein E. The Development Of A Novel Chimeric Antigen Receptor Specific For Syndecan-1. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/90143


Boston University

8. Chammas, Chantal. Gene therapy as a viable therapeutic approach for Parkinson's disease.

Degree: MS, Medical Sciences, 2019, Boston University

 Parkinson’s Disease (PD) is a neurological disorder affecting the basal ganglia in which the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc)… (more)

Subjects/Keywords: Neurosciences; Gene therapy; Parkinson's disease

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APA (6th Edition):

Chammas, C. (2019). Gene therapy as a viable therapeutic approach for Parkinson's disease. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/36248

Chicago Manual of Style (16th Edition):

Chammas, Chantal. “Gene therapy as a viable therapeutic approach for Parkinson's disease.” 2019. Masters Thesis, Boston University. Accessed September 26, 2020. http://hdl.handle.net/2144/36248.

MLA Handbook (7th Edition):

Chammas, Chantal. “Gene therapy as a viable therapeutic approach for Parkinson's disease.” 2019. Web. 26 Sep 2020.

Vancouver:

Chammas C. Gene therapy as a viable therapeutic approach for Parkinson's disease. [Internet] [Masters thesis]. Boston University; 2019. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2144/36248.

Council of Science Editors:

Chammas C. Gene therapy as a viable therapeutic approach for Parkinson's disease. [Masters Thesis]. Boston University; 2019. Available from: http://hdl.handle.net/2144/36248


University of Manitoba

9. Wang, Xiaoxia. Molecular studies on the action of APOBEC3G against HIV-1 and development of an APOBEC-based anti-HIV approach.

Degree: Medical Microbiology, 2012, University of Manitoba

 Currently, the HIV pandemic remains a major global health challenge. In order to effectively control and cure HIV-1 infection, it is necessary to perform greater… (more)

Subjects/Keywords: APOBEC3G; HIV-1; gene therapy

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APA (6th Edition):

Wang, X. (2012). Molecular studies on the action of APOBEC3G against HIV-1 and development of an APOBEC-based anti-HIV approach. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/23226

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, Xiaoxia. “Molecular studies on the action of APOBEC3G against HIV-1 and development of an APOBEC-based anti-HIV approach.” 2012. Thesis, University of Manitoba. Accessed September 26, 2020. http://hdl.handle.net/1993/23226.

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

MLA Handbook (7th Edition):

Wang, Xiaoxia. “Molecular studies on the action of APOBEC3G against HIV-1 and development of an APOBEC-based anti-HIV approach.” 2012. Web. 26 Sep 2020.

Vancouver:

Wang X. Molecular studies on the action of APOBEC3G against HIV-1 and development of an APOBEC-based anti-HIV approach. [Internet] [Thesis]. University of Manitoba; 2012. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1993/23226.

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

Council of Science Editors:

Wang X. Molecular studies on the action of APOBEC3G against HIV-1 and development of an APOBEC-based anti-HIV approach. [Thesis]. University of Manitoba; 2012. Available from: http://hdl.handle.net/1993/23226

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


University of Adelaide

10. Kremer, Karlea Lee. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery.

Degree: 2010, University of Adelaide

Gene therapy potentially holds the key for the treatment and cure of many genetic diseases, including cystic fibrosis. A number of delivery methods have been… (more)

Subjects/Keywords: cystic fibrosis; gene therapy; lentivirus

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APA (6th Edition):

Kremer, K. L. (2010). Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/63153

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):

Kremer, Karlea Lee. “Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery.” 2010. Thesis, University of Adelaide. Accessed September 26, 2020. http://hdl.handle.net/2440/63153.

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

MLA Handbook (7th Edition):

Kremer, Karlea Lee. “Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery.” 2010. Web. 26 Sep 2020.

Vancouver:

Kremer KL. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2440/63153.

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

Council of Science Editors:

Kremer KL. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/63153

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


University of Oxford

11. Orlans, Harry. Developing treatments for rhodopsin-related dominant retinitis pigmentosa.

Degree: PhD, 2019, University of Oxford

 Mutations in the rhodopsin gene are one of the most common causes of autosomal dominant retinitis pigmentosa (ADRP) and there is at present no treatment… (more)

Subjects/Keywords: Gene Therapy; Ophthalmology; Genetics

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APA (6th Edition):

Orlans, H. (2019). Developing treatments for rhodopsin-related dominant retinitis pigmentosa. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:82b393a5-aeb5-498c-9d30-d5e988d651e0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780804

Chicago Manual of Style (16th Edition):

Orlans, Harry. “Developing treatments for rhodopsin-related dominant retinitis pigmentosa.” 2019. Doctoral Dissertation, University of Oxford. Accessed September 26, 2020. http://ora.ox.ac.uk/objects/uuid:82b393a5-aeb5-498c-9d30-d5e988d651e0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780804.

MLA Handbook (7th Edition):

Orlans, Harry. “Developing treatments for rhodopsin-related dominant retinitis pigmentosa.” 2019. Web. 26 Sep 2020.

Vancouver:

Orlans H. Developing treatments for rhodopsin-related dominant retinitis pigmentosa. [Internet] [Doctoral dissertation]. University of Oxford; 2019. [cited 2020 Sep 26]. Available from: http://ora.ox.ac.uk/objects/uuid:82b393a5-aeb5-498c-9d30-d5e988d651e0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780804.

Council of Science Editors:

Orlans H. Developing treatments for rhodopsin-related dominant retinitis pigmentosa. [Doctoral Dissertation]. University of Oxford; 2019. Available from: http://ora.ox.ac.uk/objects/uuid:82b393a5-aeb5-498c-9d30-d5e988d651e0 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.780804


University of Sydney

12. McAllery, Samantha Ann. Investigating the feasibility of incorporating Vpx into lentiviral gene therapy vectors: at a global and targeted scale .

Degree: 2016, University of Sydney

 Lentiviral gene therapy has the potential to target HIV-1 reservoirs. However, a major obstacle in effectively targeting the HIV-1 latent reservoir is the lack of… (more)

Subjects/Keywords: HIV; gene therapy; virology; Vpx

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APA (6th Edition):

McAllery, S. A. (2016). Investigating the feasibility of incorporating Vpx into lentiviral gene therapy vectors: at a global and targeted scale . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/16702

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):

McAllery, Samantha Ann. “Investigating the feasibility of incorporating Vpx into lentiviral gene therapy vectors: at a global and targeted scale .” 2016. Thesis, University of Sydney. Accessed September 26, 2020. http://hdl.handle.net/2123/16702.

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

MLA Handbook (7th Edition):

McAllery, Samantha Ann. “Investigating the feasibility of incorporating Vpx into lentiviral gene therapy vectors: at a global and targeted scale .” 2016. Web. 26 Sep 2020.

Vancouver:

McAllery SA. Investigating the feasibility of incorporating Vpx into lentiviral gene therapy vectors: at a global and targeted scale . [Internet] [Thesis]. University of Sydney; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2123/16702.

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

Council of Science Editors:

McAllery SA. Investigating the feasibility of incorporating Vpx into lentiviral gene therapy vectors: at a global and targeted scale . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/16702

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


University of Toronto

13. Scaife, Matthew. Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease.

Degree: 2010, University of Toronto

Lentivirus-mediated gene therapy has curative potential for a variety of disorders, however, insertional oncogenesis still remains a concern. One approach to increase safety of such… (more)

Subjects/Keywords: gene therapy; fabry disease; 0307

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APA (6th Edition):

Scaife, M. (2010). Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25794

Chicago Manual of Style (16th Edition):

Scaife, Matthew. “Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease.” 2010. Masters Thesis, University of Toronto. Accessed September 26, 2020. http://hdl.handle.net/1807/25794.

MLA Handbook (7th Edition):

Scaife, Matthew. “Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease.” 2010. Web. 26 Sep 2020.

Vancouver:

Scaife M. Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1807/25794.

Council of Science Editors:

Scaife M. Truncated Cell Surface Markers Fused with Mutant Human Tmpk: Versatile Cell Fate Control Safety Cassettes for Lentiviral Vector Mediated Correction of Fabry Disease. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25794


Rutgers University

14. Demiryurek, Yasir, 1985-. Transport and resealing dynamics of two pulse electroporation mediated molecular delivery.

Degree: MS, Mechanical and Aerospace Engineering, 2014, Rutgers University

 Electroporation-mediated molecular delivery is of interest for many drug-delivery and gene-therapy applications. Recent studies have shown that a two-pulse protocol consisting of a short-duration high-voltage… (more)

Subjects/Keywords: Electroporation; Fluorescein; Gene therapy

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APA (6th Edition):

Demiryurek, Yasir, 1. (2014). Transport and resealing dynamics of two pulse electroporation mediated molecular delivery. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45233/

Chicago Manual of Style (16th Edition):

Demiryurek, Yasir, 1985-. “Transport and resealing dynamics of two pulse electroporation mediated molecular delivery.” 2014. Masters Thesis, Rutgers University. Accessed September 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/45233/.

MLA Handbook (7th Edition):

Demiryurek, Yasir, 1985-. “Transport and resealing dynamics of two pulse electroporation mediated molecular delivery.” 2014. Web. 26 Sep 2020.

Vancouver:

Demiryurek, Yasir 1. Transport and resealing dynamics of two pulse electroporation mediated molecular delivery. [Internet] [Masters thesis]. Rutgers University; 2014. [cited 2020 Sep 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45233/.

Council of Science Editors:

Demiryurek, Yasir 1. Transport and resealing dynamics of two pulse electroporation mediated molecular delivery. [Masters Thesis]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45233/


Rutgers University

15. Karjoo Diarkhan, Zahra, 1980-. Customization and optimization of a histone h2a-based vector for targeted gene transfer to cancer cells.

Degree: PhD, Pharmaceutical Science, 2015, Rutgers University

Developing an efficient and safe system for gene delivery is considered the bottleneck of gene therapy, where a successful delivery of the nucleic acid can… (more)

Subjects/Keywords: Gene therapy; Cancer – Treatment; Nanoparticles

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APA (6th Edition):

Karjoo Diarkhan, Zahra, 1. (2015). Customization and optimization of a histone h2a-based vector for targeted gene transfer to cancer cells. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/46367/

Chicago Manual of Style (16th Edition):

Karjoo Diarkhan, Zahra, 1980-. “Customization and optimization of a histone h2a-based vector for targeted gene transfer to cancer cells.” 2015. Doctoral Dissertation, Rutgers University. Accessed September 26, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/46367/.

MLA Handbook (7th Edition):

Karjoo Diarkhan, Zahra, 1980-. “Customization and optimization of a histone h2a-based vector for targeted gene transfer to cancer cells.” 2015. Web. 26 Sep 2020.

Vancouver:

Karjoo Diarkhan, Zahra 1. Customization and optimization of a histone h2a-based vector for targeted gene transfer to cancer cells. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2020 Sep 26]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46367/.

Council of Science Editors:

Karjoo Diarkhan, Zahra 1. Customization and optimization of a histone h2a-based vector for targeted gene transfer to cancer cells. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/46367/


Rice University

16. Robinson, Tawana M. Engineering Adeno-Associated Virus for Protease Targeted Gene Therapy and Immune Avoidance.

Degree: PhD, Natural Sciences, 2019, Rice University

 Adeno-associated virus (AAV) has earned significant attention as a safe and efficient gene therapy tool. AAV has been used in over 100 clinical trials to… (more)

Subjects/Keywords: Adeno-associated; virus; gene therapy

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APA (6th Edition):

Robinson, T. M. (2019). Engineering Adeno-Associated Virus for Protease Targeted Gene Therapy and Immune Avoidance. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/106024

Chicago Manual of Style (16th Edition):

Robinson, Tawana M. “Engineering Adeno-Associated Virus for Protease Targeted Gene Therapy and Immune Avoidance.” 2019. Doctoral Dissertation, Rice University. Accessed September 26, 2020. http://hdl.handle.net/1911/106024.

MLA Handbook (7th Edition):

Robinson, Tawana M. “Engineering Adeno-Associated Virus for Protease Targeted Gene Therapy and Immune Avoidance.” 2019. Web. 26 Sep 2020.

Vancouver:

Robinson TM. Engineering Adeno-Associated Virus for Protease Targeted Gene Therapy and Immune Avoidance. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1911/106024.

Council of Science Editors:

Robinson TM. Engineering Adeno-Associated Virus for Protease Targeted Gene Therapy and Immune Avoidance. [Doctoral Dissertation]. Rice University; 2019. Available from: http://hdl.handle.net/1911/106024

17. Pouw, Nadine. Towards effective TCR gene therapy: preclinical requirements.

Degree: 2010, Erasmus University Medical Center

Subjects/Keywords: gene therapy

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APA (6th Edition):

Pouw, N. (2010). Towards effective TCR gene therapy: preclinical requirements. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/38592

Chicago Manual of Style (16th Edition):

Pouw, Nadine. “Towards effective TCR gene therapy: preclinical requirements.” 2010. Doctoral Dissertation, Erasmus University Medical Center. Accessed September 26, 2020. http://hdl.handle.net/1765/38592.

MLA Handbook (7th Edition):

Pouw, Nadine. “Towards effective TCR gene therapy: preclinical requirements.” 2010. Web. 26 Sep 2020.

Vancouver:

Pouw N. Towards effective TCR gene therapy: preclinical requirements. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2010. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1765/38592.

Council of Science Editors:

Pouw N. Towards effective TCR gene therapy: preclinical requirements. [Doctoral Dissertation]. Erasmus University Medical Center; 2010. Available from: http://hdl.handle.net/1765/38592


University of Minnesota

18. Ou, Li. Molecular Therapy and Gene Therapy for Hurler Syndrome.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2015, University of Minnesota

 Mucopolysaccharidosis type I (MPS I) is an autosomal recessive disease which leads to systemic disease, including progressive neurodegeneration, mental retardation and death before the age… (more)

Subjects/Keywords: gene therapy; Hurler syndrome

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APA (6th Edition):

Ou, L. (2015). Molecular Therapy and Gene Therapy for Hurler Syndrome. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/175288

Chicago Manual of Style (16th Edition):

Ou, Li. “Molecular Therapy and Gene Therapy for Hurler Syndrome.” 2015. Doctoral Dissertation, University of Minnesota. Accessed September 26, 2020. http://hdl.handle.net/11299/175288.

MLA Handbook (7th Edition):

Ou, Li. “Molecular Therapy and Gene Therapy for Hurler Syndrome.” 2015. Web. 26 Sep 2020.

Vancouver:

Ou L. Molecular Therapy and Gene Therapy for Hurler Syndrome. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/11299/175288.

Council of Science Editors:

Ou L. Molecular Therapy and Gene Therapy for Hurler Syndrome. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/175288

19. Vrins, Carlos. Modulation of gene expression in the liver: towards targeted correction of hyperlipidemia.

Degree: 2005, Leiden University, Faculty of Mathematics & Natural Sciences, Leiden/Amsterdam Center for Drug Research

Subjects/Keywords: Gene therapy

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APA (6th Edition):

Vrins, C. (2005). Modulation of gene expression in the liver: towards targeted correction of hyperlipidemia. (Doctoral Dissertation). Leiden University, Faculty of Mathematics & Natural Sciences, Leiden/Amsterdam Center for Drug Research. Retrieved from http://hdl.handle.net/1887/632

Chicago Manual of Style (16th Edition):

Vrins, Carlos. “Modulation of gene expression in the liver: towards targeted correction of hyperlipidemia.” 2005. Doctoral Dissertation, Leiden University, Faculty of Mathematics & Natural Sciences, Leiden/Amsterdam Center for Drug Research. Accessed September 26, 2020. http://hdl.handle.net/1887/632.

MLA Handbook (7th Edition):

Vrins, Carlos. “Modulation of gene expression in the liver: towards targeted correction of hyperlipidemia.” 2005. Web. 26 Sep 2020.

Vancouver:

Vrins C. Modulation of gene expression in the liver: towards targeted correction of hyperlipidemia. [Internet] [Doctoral dissertation]. Leiden University, Faculty of Mathematics & Natural Sciences, Leiden/Amsterdam Center for Drug Research; 2005. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1887/632.

Council of Science Editors:

Vrins C. Modulation of gene expression in the liver: towards targeted correction of hyperlipidemia. [Doctoral Dissertation]. Leiden University, Faculty of Mathematics & Natural Sciences, Leiden/Amsterdam Center for Drug Research; 2005. Available from: http://hdl.handle.net/1887/632

20. Mastorakos, Panagiotis. Γονιδιακή θεραπεία νόσων του κεντρικού νευρικού συστήματος.

Degree: 2017, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Gene therapy is a novel tool for treating central nervous system diseases with unfavorable prognosis. Despite the promising results of multiple clinical studies, the limited… (more)

Subjects/Keywords: Γονιδιακή θεραπεία; Gene therapy

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APA (6th Edition):

Mastorakos, P. (2017). Γονιδιακή θεραπεία νόσων του κεντρικού νευρικού συστήματος. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/42189

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):

Mastorakos, Panagiotis. “Γονιδιακή θεραπεία νόσων του κεντρικού νευρικού συστήματος.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed September 26, 2020. http://hdl.handle.net/10442/hedi/42189.

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

MLA Handbook (7th Edition):

Mastorakos, Panagiotis. “Γονιδιακή θεραπεία νόσων του κεντρικού νευρικού συστήματος.” 2017. Web. 26 Sep 2020.

Vancouver:

Mastorakos P. Γονιδιακή θεραπεία νόσων του κεντρικού νευρικού συστήματος. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10442/hedi/42189.

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

Council of Science Editors:

Mastorakos P. Γονιδιακή θεραπεία νόσων του κεντρικού νευρικού συστήματος. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/42189

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


University of Missouri – Columbia

21. Korampally, Madhuri. Fabrication and characterization of micro-chip based shockwave generator for particle delivery and cell transfection.

Degree: 2014, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Shock waves have potential applications in many areas such as in geology, seismological techniques, and… (more)

Subjects/Keywords: Shock waves; Gene therapy; Nanoparticles

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APA (6th Edition):

Korampally, M. (2014). Fabrication and characterization of micro-chip based shockwave generator for particle delivery and cell transfection. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/45908

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):

Korampally, Madhuri. “Fabrication and characterization of micro-chip based shockwave generator for particle delivery and cell transfection.” 2014. Thesis, University of Missouri – Columbia. Accessed September 26, 2020. http://hdl.handle.net/10355/45908.

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

MLA Handbook (7th Edition):

Korampally, Madhuri. “Fabrication and characterization of micro-chip based shockwave generator for particle delivery and cell transfection.” 2014. Web. 26 Sep 2020.

Vancouver:

Korampally M. Fabrication and characterization of micro-chip based shockwave generator for particle delivery and cell transfection. [Internet] [Thesis]. University of Missouri – Columbia; 2014. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10355/45908.

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

Council of Science Editors:

Korampally M. Fabrication and characterization of micro-chip based shockwave generator for particle delivery and cell transfection. [Thesis]. University of Missouri – Columbia; 2014. Available from: http://hdl.handle.net/10355/45908

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


California State University – Sacramento

22. Cicchetto, Andrew C. Genetically modified multipotent stromal cells for the treatment of osteoarthritis.

Degree: MA, Biological Science (Stem Cell, 2016, California State University – Sacramento

 Osteoarthritis (OA) is a degenerative joint disease estimated to affect 630 million people worldwide. OA is characterized by the progressive loss of articular cartilage, damage… (more)

Subjects/Keywords: Interleukin-10; Gene Therapy; Cell Therapy; Lentivirus

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APA (6th Edition):

Cicchetto, A. C. (2016). Genetically modified multipotent stromal cells for the treatment of osteoarthritis. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/171158

Chicago Manual of Style (16th Edition):

Cicchetto, Andrew C. “Genetically modified multipotent stromal cells for the treatment of osteoarthritis.” 2016. Masters Thesis, California State University – Sacramento. Accessed September 26, 2020. http://hdl.handle.net/10211.3/171158.

MLA Handbook (7th Edition):

Cicchetto, Andrew C. “Genetically modified multipotent stromal cells for the treatment of osteoarthritis.” 2016. Web. 26 Sep 2020.

Vancouver:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10211.3/171158.

Council of Science Editors:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Masters Thesis]. California State University – Sacramento; 2016. Available from: http://hdl.handle.net/10211.3/171158

23. Kobayashi, Yuji. Effects of Fibrotic Tissue on Liver-targeted Hydrodynamic Gene Delivery. : 肝臓選択的ハイドロダイナミック遺伝子導入法において、線維組織が導入効率に与える影響.

Degree: 博士(医学), 2017, Niigata University / 新潟大学

学位の種類: 博士(医学). 報告番号: 甲第4252号. 学位記番号: 新大院博(医)甲第730号. 学位授与年月日: 平成29年3月23日

Molecular Therapy. Nucleic Acids 5(8) e359 2016

Hydrodynamic gene delivery is a common method for gene transfer… (more)

Subjects/Keywords: gene therapy; hydrodynamic gene delivery; liver fibrosis; MMP13; nonviral gene delivery

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APA (6th Edition):

Kobayashi, Y. (2017). Effects of Fibrotic Tissue on Liver-targeted Hydrodynamic Gene Delivery. : 肝臓選択的ハイドロダイナミック遺伝子導入法において、線維組織が導入効率に与える影響. (Thesis). Niigata University / 新潟大学. Retrieved from http://hdl.handle.net/10191/47583

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):

Kobayashi, Yuji. “Effects of Fibrotic Tissue on Liver-targeted Hydrodynamic Gene Delivery. : 肝臓選択的ハイドロダイナミック遺伝子導入法において、線維組織が導入効率に与える影響.” 2017. Thesis, Niigata University / 新潟大学. Accessed September 26, 2020. http://hdl.handle.net/10191/47583.

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

MLA Handbook (7th Edition):

Kobayashi, Yuji. “Effects of Fibrotic Tissue on Liver-targeted Hydrodynamic Gene Delivery. : 肝臓選択的ハイドロダイナミック遺伝子導入法において、線維組織が導入効率に与える影響.” 2017. Web. 26 Sep 2020.

Vancouver:

Kobayashi Y. Effects of Fibrotic Tissue on Liver-targeted Hydrodynamic Gene Delivery. : 肝臓選択的ハイドロダイナミック遺伝子導入法において、線維組織が導入効率に与える影響. [Internet] [Thesis]. Niigata University / 新潟大学; 2017. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10191/47583.

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

Council of Science Editors:

Kobayashi Y. Effects of Fibrotic Tissue on Liver-targeted Hydrodynamic Gene Delivery. : 肝臓選択的ハイドロダイナミック遺伝子導入法において、線維組織が導入効率に与える影響. [Thesis]. Niigata University / 新潟大学; 2017. Available from: http://hdl.handle.net/10191/47583

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

24. Davis, Martin. Gene Editing and Human Flourishing.

Degree: 2020, The Catholic University of America

The advent of gene editing technology brings with it new ethical challenges. Among these challenges is the question of what kinds of gene editing should… (more)

Subjects/Keywords: Enhancement; Ethics; Gene Editing; Gene Enhancement; Gene Therapy; Human Flourishing

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APA (6th Edition):

Davis, M. (2020). Gene Editing and Human Flourishing. (Thesis). The Catholic University of America. Retrieved from http://hdl.handle.net/1961/cuislandora:214557

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):

Davis, Martin. “Gene Editing and Human Flourishing.” 2020. Thesis, The Catholic University of America. Accessed September 26, 2020. http://hdl.handle.net/1961/cuislandora:214557.

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

MLA Handbook (7th Edition):

Davis, Martin. “Gene Editing and Human Flourishing.” 2020. Web. 26 Sep 2020.

Vancouver:

Davis M. Gene Editing and Human Flourishing. [Internet] [Thesis]. The Catholic University of America; 2020. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/1961/cuislandora:214557.

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

Council of Science Editors:

Davis M. Gene Editing and Human Flourishing. [Thesis]. The Catholic University of America; 2020. Available from: http://hdl.handle.net/1961/cuislandora:214557

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


Massey University

25. Yang, Tian. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.

Degree: MSc, Biochemistry, 2013, Massey University

 Lentiviral vectors, originally derived from human immunodeficiency virus, provide highly efficient viral gene delivery vehicles. Lentiviral vectors often use a constitutive promoter to drive the… (more)

Subjects/Keywords: Lentiviral vectors; Gene therapy; Gene expression; Gene regulation; Tetracycline; Genetic vectors

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APA (6th Edition):

Yang, T. (2013). Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. (Masters Thesis). Massey University. Retrieved from http://hdl.handle.net/10179/4319

Chicago Manual of Style (16th Edition):

Yang, Tian. “Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.” 2013. Masters Thesis, Massey University. Accessed September 26, 2020. http://hdl.handle.net/10179/4319.

MLA Handbook (7th Edition):

Yang, Tian. “Development of a tetracycline-inducible lentiviral vector with an instant regulatory system.” 2013. Web. 26 Sep 2020.

Vancouver:

Yang T. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. [Internet] [Masters thesis]. Massey University; 2013. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10179/4319.

Council of Science Editors:

Yang T. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. [Masters Thesis]. Massey University; 2013. Available from: http://hdl.handle.net/10179/4319


University College Cork

26. Sadadcharam, Mira. Expanding the use of electroporation from cutaneous to intraluminal and systemic applications.

Degree: 2015, University College Cork

 Cancer is a global phenomenon transcending the boundaries of age, race, geography and socioeconomic background. As our understanding of cancer cell biology has improved, we… (more)

Subjects/Keywords: Electroporation; Electrochemotherapy; EndoVe; Cancer immunogene therapy; Immune therapy; Gene therapy

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APA (6th Edition):

Sadadcharam, M. (2015). Expanding the use of electroporation from cutaneous to intraluminal and systemic applications. (Thesis). University College Cork. Retrieved from http://hdl.handle.net/10468/3484

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):

Sadadcharam, Mira. “Expanding the use of electroporation from cutaneous to intraluminal and systemic applications.” 2015. Thesis, University College Cork. Accessed September 26, 2020. http://hdl.handle.net/10468/3484.

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

MLA Handbook (7th Edition):

Sadadcharam, Mira. “Expanding the use of electroporation from cutaneous to intraluminal and systemic applications.” 2015. Web. 26 Sep 2020.

Vancouver:

Sadadcharam M. Expanding the use of electroporation from cutaneous to intraluminal and systemic applications. [Internet] [Thesis]. University College Cork; 2015. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/10468/3484.

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

Council of Science Editors:

Sadadcharam M. Expanding the use of electroporation from cutaneous to intraluminal and systemic applications. [Thesis]. University College Cork; 2015. Available from: http://hdl.handle.net/10468/3484

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


University of California – Berkeley

27. Bai, Yong. In vivo Delivery of Catalytic RNase P Ribozyme as an Antiviral Agent.

Degree: Comparative Biochemistry, 2010, University of California – Berkeley

 Engineered M1GS ribozyme derived from RNA subunit of E. coli can be a very promising antiviral agent. The focus of this dissertation has been to… (more)

Subjects/Keywords: Biology; Virology; CMV; delivery; gene therapy; Ribozyme

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APA (6th Edition):

Bai, Y. (2010). In vivo Delivery of Catalytic RNase P Ribozyme as an Antiviral Agent. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/5kx3k87c

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):

Bai, Yong. “In vivo Delivery of Catalytic RNase P Ribozyme as an Antiviral Agent.” 2010. Thesis, University of California – Berkeley. Accessed September 26, 2020. http://www.escholarship.org/uc/item/5kx3k87c.

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

MLA Handbook (7th Edition):

Bai, Yong. “In vivo Delivery of Catalytic RNase P Ribozyme as an Antiviral Agent.” 2010. Web. 26 Sep 2020.

Vancouver:

Bai Y. In vivo Delivery of Catalytic RNase P Ribozyme as an Antiviral Agent. [Internet] [Thesis]. University of California – Berkeley; 2010. [cited 2020 Sep 26]. Available from: http://www.escholarship.org/uc/item/5kx3k87c.

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

Council of Science Editors:

Bai Y. In vivo Delivery of Catalytic RNase P Ribozyme as an Antiviral Agent. [Thesis]. University of California – Berkeley; 2010. Available from: http://www.escholarship.org/uc/item/5kx3k87c

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


University of California – San Diego

28. Corleto, Jose Alfredo. Electrophysiological and neurological characterization of a thoracic 9 model of spinal cord injury-induced muscle spasticity and the therapeutic anti-spastic effect following spinal GAD65 gene delivery in the rat.

Degree: Biomedical Sciences, 2016, University of California – San Diego

 Spinal cord injury is a problem that carries with it many implications including changes in motor circuit action that then lead to development of muscle… (more)

Subjects/Keywords: Biology; Gene Therapy; Pharmacology; Spinal Cord Injury

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APA (6th Edition):

Corleto, J. A. (2016). Electrophysiological and neurological characterization of a thoracic 9 model of spinal cord injury-induced muscle spasticity and the therapeutic anti-spastic effect following spinal GAD65 gene delivery in the rat. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/64h01790

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):

Corleto, Jose Alfredo. “Electrophysiological and neurological characterization of a thoracic 9 model of spinal cord injury-induced muscle spasticity and the therapeutic anti-spastic effect following spinal GAD65 gene delivery in the rat.” 2016. Thesis, University of California – San Diego. Accessed September 26, 2020. http://www.escholarship.org/uc/item/64h01790.

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

MLA Handbook (7th Edition):

Corleto, Jose Alfredo. “Electrophysiological and neurological characterization of a thoracic 9 model of spinal cord injury-induced muscle spasticity and the therapeutic anti-spastic effect following spinal GAD65 gene delivery in the rat.” 2016. Web. 26 Sep 2020.

Vancouver:

Corleto JA. Electrophysiological and neurological characterization of a thoracic 9 model of spinal cord injury-induced muscle spasticity and the therapeutic anti-spastic effect following spinal GAD65 gene delivery in the rat. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Sep 26]. Available from: http://www.escholarship.org/uc/item/64h01790.

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

Council of Science Editors:

Corleto JA. Electrophysiological and neurological characterization of a thoracic 9 model of spinal cord injury-induced muscle spasticity and the therapeutic anti-spastic effect following spinal GAD65 gene delivery in the rat. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/64h01790

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


University of Sydney

29. Wootton, Virginia. Evaluation of lentivirus-mediated reconstitution of the B-cell compartment in XLA patient-derived CD34+ cells in humanised mice .

Degree: 2016, University of Sydney

 X-Linked Agammaglobulinaemia (XLA) is a primary immune deficiency resulting in an absence of B-cells and antibody production due to mutations in the Bruton’s tyrosine kinase… (more)

Subjects/Keywords: Humanised mouse model; XLA gene therapy

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

APA (6th Edition):

Wootton, V. (2016). Evaluation of lentivirus-mediated reconstitution of the B-cell compartment in XLA patient-derived CD34+ cells in humanised mice . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/15864

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):

Wootton, Virginia. “Evaluation of lentivirus-mediated reconstitution of the B-cell compartment in XLA patient-derived CD34+ cells in humanised mice .” 2016. Thesis, University of Sydney. Accessed September 26, 2020. http://hdl.handle.net/2123/15864.

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

MLA Handbook (7th Edition):

Wootton, Virginia. “Evaluation of lentivirus-mediated reconstitution of the B-cell compartment in XLA patient-derived CD34+ cells in humanised mice .” 2016. Web. 26 Sep 2020.

Vancouver:

Wootton V. Evaluation of lentivirus-mediated reconstitution of the B-cell compartment in XLA patient-derived CD34+ cells in humanised mice . [Internet] [Thesis]. University of Sydney; 2016. [cited 2020 Sep 26]. Available from: http://hdl.handle.net/2123/15864.

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

Council of Science Editors:

Wootton V. Evaluation of lentivirus-mediated reconstitution of the B-cell compartment in XLA patient-derived CD34+ cells in humanised mice . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/15864

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


University of Utah

30. Christensen, Lane. Reducible poly(amido ethylenimine)s for gene delivery;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2007, University of Utah

 Much has been learned from the success and, more so, from the early failures of gene therapy, thereby providing a realistic therapeutic alternative for a… (more)

Subjects/Keywords: Polymetric Drug Delivery System; Gene Therapy

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

APA (6th Edition):

Christensen, L. (2007). Reducible poly(amido ethylenimine)s for gene delivery;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085

Chicago Manual of Style (16th Edition):

Christensen, Lane. “Reducible poly(amido ethylenimine)s for gene delivery;.” 2007. Doctoral Dissertation, University of Utah. Accessed September 26, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085.

MLA Handbook (7th Edition):

Christensen, Lane. “Reducible poly(amido ethylenimine)s for gene delivery;.” 2007. Web. 26 Sep 2020.

Vancouver:

Christensen L. Reducible poly(amido ethylenimine)s for gene delivery;. [Internet] [Doctoral dissertation]. University of Utah; 2007. [cited 2020 Sep 26]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085.

Council of Science Editors:

Christensen L. Reducible poly(amido ethylenimine)s for gene delivery;. [Doctoral Dissertation]. University of Utah; 2007. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/1611/rec/1085

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