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You searched for subject:(Gene therapy). Showing records 1 – 30 of 1141 total matches.

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University of Georgia

1. Kabiru, Paul. DNA condensation and packaging for potential application in gene therapy.

Degree: MS, Chemistry, 2009, University of Georgia

 The phenomenon of DNA condensation has been studied for decades, often as a model of DNA packaging within viruses and chromosomes, due to its medical… (more)

Subjects/Keywords: Gene Therapy

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

APA (6th Edition):

Kabiru, P. (2009). DNA condensation and packaging for potential application in gene therapy. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/kabiru_paul_k_200908_ms

Chicago Manual of Style (16th Edition):

Kabiru, Paul. “DNA condensation and packaging for potential application in gene therapy.” 2009. Masters Thesis, University of Georgia. Accessed April 07, 2020. http://purl.galileo.usg.edu/uga_etd/kabiru_paul_k_200908_ms.

MLA Handbook (7th Edition):

Kabiru, Paul. “DNA condensation and packaging for potential application in gene therapy.” 2009. Web. 07 Apr 2020.

Vancouver:

Kabiru P. DNA condensation and packaging for potential application in gene therapy. [Internet] [Masters thesis]. University of Georgia; 2009. [cited 2020 Apr 07]. Available from: http://purl.galileo.usg.edu/uga_etd/kabiru_paul_k_200908_ms.

Council of Science Editors:

Kabiru P. DNA condensation and packaging for potential application in gene therapy. [Masters Thesis]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/kabiru_paul_k_200908_ms


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 April 07, 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. 07 Apr 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 Apr 07]. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Ellis BL. Improving Viral Vectors for Gene Targeting in Gene Therapy. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Apr 07]. 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


Texas A&M University

4. Chern, Christina. The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications.

Degree: 2009, Texas A&M University

 The study of drug delivery for the treatment of illnesses and injuries is an important area of pharmaceutical technology. A relatively new area of drug… (more)

Subjects/Keywords: gene therapy; siRNA

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APA (6th Edition):

Chern, C. (2009). The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2327

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):

Chern, Christina. “The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications.” 2009. Thesis, Texas A&M University. Accessed April 07, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2327.

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

MLA Handbook (7th Edition):

Chern, Christina. “The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications.” 2009. Web. 07 Apr 2020.

Vancouver:

Chern C. The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2327.

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

Council of Science Editors:

Chern C. The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2327

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


Rutgers University

5. 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 April 07, 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. 07 Apr 2020.

Vancouver:

FENG, XING 1. Roles of SETD4 in radiation sensitivity and tumorigenesis. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2020 Apr 07]. 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 Hong Kong

6. Chan, Fu-lun. Effective DNA delivery mediated by pH responsive peptides.

Degree: Master of Medical Sciences, 2012, University of Hong Kong

Non-viral vectors have been used to deliver therapeutic genes to treat different diseases. There are a variety of non-viral vectors such as liposomes, cationic polymers… (more)

Subjects/Keywords: Peptides.; Gene targeting.; Genetic vectors.; Gene therapy.

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APA (6th Edition):

Chan, F. (2012). Effective DNA delivery mediated by pH responsive peptides. (Masters Thesis). University of Hong Kong. Retrieved from Chan, F. [陳賦麟]. (2012). Effective DNA delivery mediated by pH responsive peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833333 ; http://dx.doi.org/10.5353/th_b4833333 ; http://hdl.handle.net/10722/173921

Chicago Manual of Style (16th Edition):

Chan, Fu-lun. “Effective DNA delivery mediated by pH responsive peptides.” 2012. Masters Thesis, University of Hong Kong. Accessed April 07, 2020. Chan, F. [陳賦麟]. (2012). Effective DNA delivery mediated by pH responsive peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833333 ; http://dx.doi.org/10.5353/th_b4833333 ; http://hdl.handle.net/10722/173921.

MLA Handbook (7th Edition):

Chan, Fu-lun. “Effective DNA delivery mediated by pH responsive peptides.” 2012. Web. 07 Apr 2020.

Vancouver:

Chan F. Effective DNA delivery mediated by pH responsive peptides. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2020 Apr 07]. Available from: Chan, F. [陳賦麟]. (2012). Effective DNA delivery mediated by pH responsive peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833333 ; http://dx.doi.org/10.5353/th_b4833333 ; http://hdl.handle.net/10722/173921.

Council of Science Editors:

Chan F. Effective DNA delivery mediated by pH responsive peptides. [Masters Thesis]. University of Hong Kong; 2012. Available from: Chan, F. [陳賦麟]. (2012). Effective DNA delivery mediated by pH responsive peptides. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833333 ; http://dx.doi.org/10.5353/th_b4833333 ; http://hdl.handle.net/10722/173921


University of Texas Southwestern Medical Center

7. 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 April 07, 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. 07 Apr 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 Apr 07]. 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 Edinburgh

8. Jannetta, Evelyn Elena. Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy.

Degree: Thesis (D.Clin.Psy.), 2009, University of Edinburgh

 Introduction: Gene therapy is currently being developed for people with cystic fibrosis (CF), a life-threatening condition for which there is no cure. The UK CF… (more)

Subjects/Keywords: Cystic fibrosis; Gene therapy; Expectations

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APA (6th Edition):

Jannetta, E. E. (2009). Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8745

Chicago Manual of Style (16th Edition):

Jannetta, Evelyn Elena. “Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy.” 2009. Doctoral Dissertation, University of Edinburgh. Accessed April 07, 2020. http://hdl.handle.net/1842/8745.

MLA Handbook (7th Edition):

Jannetta, Evelyn Elena. “Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy.” 2009. Web. 07 Apr 2020.

Vancouver:

Jannetta EE. Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy. [Internet] [Doctoral dissertation]. University of Edinburgh; 2009. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/1842/8745.

Council of Science Editors:

Jannetta EE. Qualitative study of cystic fibrosis (CF) patients' expectations of gene therapy. [Doctoral Dissertation]. University of Edinburgh; 2009. Available from: http://hdl.handle.net/1842/8745


University of KwaZulu-Natal

9. [No author]. Novel siRNA lipoplexes : their targeted and untargeted delivery to mammalian cells in culture.

Degree: Genetics, 2011, University of KwaZulu-Natal

 The high gene knockdown specificity and efficiency of RNA interference (RNAi) provides a potentially viable avenue for the development of a new class of nucleic… (more)

Subjects/Keywords: RNA.; Liposomes.; Gene therapy.; Genetics.

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APA (6th Edition):

author], [. (2011). Novel siRNA lipoplexes : their targeted and untargeted delivery to mammalian cells in culture. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/11134

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):

author], [No. “Novel siRNA lipoplexes : their targeted and untargeted delivery to mammalian cells in culture. ” 2011. Thesis, University of KwaZulu-Natal. Accessed April 07, 2020. http://hdl.handle.net/10413/11134.

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

MLA Handbook (7th Edition):

author], [No. “Novel siRNA lipoplexes : their targeted and untargeted delivery to mammalian cells in culture. ” 2011. Web. 07 Apr 2020.

Vancouver:

author] [. Novel siRNA lipoplexes : their targeted and untargeted delivery to mammalian cells in culture. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/10413/11134.

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

Council of Science Editors:

author] [. Novel siRNA lipoplexes : their targeted and untargeted delivery to mammalian cells in culture. [Thesis]. University of KwaZulu-Natal; 2011. Available from: http://hdl.handle.net/10413/11134

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

10. 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 April 07, 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. 07 Apr 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 Apr 07]. 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 Rochester

11. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Badding M. Cytoplasmic Factors that Impact Intracellular Plasmid Trafficking During Gene Transfer. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2020 Apr 07]. 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


Boston University

12. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Chammas C. Gene therapy as a viable therapeutic approach for Parkinson's disease. [Internet] [Masters thesis]. Boston University; 2019. [cited 2020 Apr 07]. 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 Toronto

13. 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 April 07, 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. 07 Apr 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 Apr 07]. 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


University of Oxford

14. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Orlans H. Developing treatments for rhodopsin-related dominant retinitis pigmentosa. [Internet] [Doctoral dissertation]. University of Oxford; 2019. [cited 2020 Apr 07]. 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 Manitoba

15. 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 April 07, 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. 07 Apr 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 Apr 07]. 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

16. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Kremer KL. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2020 Apr 07]. 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 Sydney

17. 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 April 07, 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. 07 Apr 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 Apr 07]. 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

18. 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 April 07, 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. 07 Apr 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 Apr 07]. 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

19. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Demiryurek, Yasir 1. Transport and resealing dynamics of two pulse electroporation mediated molecular delivery. [Internet] [Masters thesis]. Rutgers University; 2014. [cited 2020 Apr 07]. 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

20. 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 April 07, 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. 07 Apr 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 Apr 07]. 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/

21. 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 April 07, 2020. http://hdl.handle.net/1765/38592.

MLA Handbook (7th Edition):

Pouw, Nadine. “Towards effective TCR gene therapy: preclinical requirements.” 2010. Web. 07 Apr 2020.

Vancouver:

Pouw N. Towards effective TCR gene therapy: preclinical requirements. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2010. [cited 2020 Apr 07]. 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


Rice University

22. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Robinson TM. Engineering Adeno-Associated Virus for Protease Targeted Gene Therapy and Immune Avoidance. [Internet] [Doctoral dissertation]. Rice University; 2019. [cited 2020 Apr 07]. 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

23. 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 April 07, 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. 07 Apr 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 Apr 07]. 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


University of Minnesota

24. 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 April 07, 2020. http://hdl.handle.net/11299/175288.

MLA Handbook (7th Edition):

Ou, Li. “Molecular Therapy and Gene Therapy for Hurler Syndrome.” 2015. Web. 07 Apr 2020.

Vancouver:

Ou L. Molecular Therapy and Gene Therapy for Hurler Syndrome. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2020 Apr 07]. 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


University of Missouri – Columbia

25. 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 April 07, 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. 07 Apr 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 Apr 07]. 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

26. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2020 Apr 07]. 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

27. 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 April 07, 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. 07 Apr 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 Apr 07]. 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


Massey University

28. 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 April 07, 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. 07 Apr 2020.

Vancouver:

Yang T. Development of a tetracycline-inducible lentiviral vector with an instant regulatory system. [Internet] [Masters thesis]. Massey University; 2013. [cited 2020 Apr 07]. 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

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

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 April 07, 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. 07 Apr 2020.

Vancouver:

Sadadcharam M. Expanding the use of electroporation from cutaneous to intraluminal and systemic applications. [Internet] [Thesis]. University College Cork; 2015. [cited 2020 Apr 07]. 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 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 April 07, 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. 07 Apr 2020.

Vancouver:

Christensen L. Reducible poly(amido ethylenimine)s for gene delivery;. [Internet] [Doctoral dissertation]. University of Utah; 2007. [cited 2020 Apr 07]. 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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