Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(Genetherapy). Showing records 1 – 10 of 10 total matches.

Search Limiters

Last 2 Years | English Only

No search limiters apply to these results.

▼ Search Limiters


University of Manchester

1. Faqih, Layla Ahmed A. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.

Degree: 2018, University of Manchester

 Production of an effective vaccine and long-term treatment against human immunodeficiency virus (HIV) is elusive. In this thesis two different techniques were used in an… (more)

Subjects/Keywords: HIV; SIV; Genetherapy; Immunotherapy; Vaccination; Baculovirus; BacMam

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Faqih, L. A. A. (2018). HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559

Chicago Manual of Style (16th Edition):

Faqih, Layla Ahmed A. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Doctoral Dissertation, University of Manchester. Accessed September 23, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559.

MLA Handbook (7th Edition):

Faqih, Layla Ahmed A. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Web. 23 Sep 2020.

Vancouver:

Faqih LAA. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Sep 23]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559.

Council of Science Editors:

Faqih LAA. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:315559

2. Faqih, Layla. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.

Degree: PhD, 2018, University of Manchester

 Production of an effective vaccine and long-term treatment against human immunodeficiency virus (HIV) is elusive. In this thesis two different techniques were used in an… (more)

Subjects/Keywords: Vaccination; Baculovirus; BacMam; Genetherapy; SIV; HIV; Immunotherapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Faqih, L. (2018). HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895

Chicago Manual of Style (16th Edition):

Faqih, Layla. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Doctoral Dissertation, University of Manchester. Accessed September 23, 2020. https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895.

MLA Handbook (7th Edition):

Faqih, Layla. “HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems.” 2018. Web. 23 Sep 2020.

Vancouver:

Faqih L. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Sep 23]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895.

Council of Science Editors:

Faqih L. HIV neutralising antibody delivered by gene therapy with a hybrid Vaccinia/retrovirus or BacMam/retrovirus expression systems. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/hiv-neutralising-antibody-delivered-by-gene-therapy-with-a-hybrid-vacciniaretrovirus-or-bacmamretrovirus-expression-systems(b540de64-0484-461c-9ccf-a59ae3681f7f).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756895

3. Thakur, Sarjeet Singh. Enzyme and gene therapy using oxalate degrading enzyme for kidney stone treatment; -.

Degree: Medicine, 2008, Jawaharlal Nehru University

None

Bibliography Given

Advisors/Committee Members: Datta, Asis.

Subjects/Keywords: kidney stone; Enzyme; genetherapy; oxalate

Page 1

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thakur, S. S. (2008). Enzyme and gene therapy using oxalate degrading enzyme for kidney stone treatment; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/22150

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):

Thakur, Sarjeet Singh. “Enzyme and gene therapy using oxalate degrading enzyme for kidney stone treatment; -.” 2008. Thesis, Jawaharlal Nehru University. Accessed September 23, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/22150.

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

MLA Handbook (7th Edition):

Thakur, Sarjeet Singh. “Enzyme and gene therapy using oxalate degrading enzyme for kidney stone treatment; -.” 2008. Web. 23 Sep 2020.

Vancouver:

Thakur SS. Enzyme and gene therapy using oxalate degrading enzyme for kidney stone treatment; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2008. [cited 2020 Sep 23]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/22150.

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

Council of Science Editors:

Thakur SS. Enzyme and gene therapy using oxalate degrading enzyme for kidney stone treatment; -. [Thesis]. Jawaharlal Nehru University; 2008. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/22150

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


Universitat Autònoma de Barcelona

4. Garcia Moure, Marc. Generación de una adenovirus Ad5/52s pseudotipado con la proteína fiber corta del Ad52 para su caracterización in vitro e in vivo como vector de terapia génica.

Degree: Departament de Bioquímica i Biologia Molecular, 2016, Universitat Autònoma de Barcelona

 Gene therapy is a biomedical approach, which consists of manipulating and delivering genes to treat a wide range of diseases. Nevertheless, a successful treatment also… (more)

Subjects/Keywords: Adenovirus quimèrics; Adenovirus quiméricos; Chimeric adenoviruses; Teràpia gènica; Terapia génica; Genetherapy; Fibra; Fiber; Ciències Experimentals; 577

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garcia Moure, M. (2016). Generación de una adenovirus Ad5/52s pseudotipado con la proteína fiber corta del Ad52 para su caracterización in vitro e in vivo como vector de terapia génica. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/370116

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):

Garcia Moure, Marc. “Generación de una adenovirus Ad5/52s pseudotipado con la proteína fiber corta del Ad52 para su caracterización in vitro e in vivo como vector de terapia génica.” 2016. Thesis, Universitat Autònoma de Barcelona. Accessed September 23, 2020. http://hdl.handle.net/10803/370116.

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

MLA Handbook (7th Edition):

Garcia Moure, Marc. “Generación de una adenovirus Ad5/52s pseudotipado con la proteína fiber corta del Ad52 para su caracterización in vitro e in vivo como vector de terapia génica.” 2016. Web. 23 Sep 2020.

Vancouver:

Garcia Moure M. Generación de una adenovirus Ad5/52s pseudotipado con la proteína fiber corta del Ad52 para su caracterización in vitro e in vivo como vector de terapia génica. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10803/370116.

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

Council of Science Editors:

Garcia Moure M. Generación de una adenovirus Ad5/52s pseudotipado con la proteína fiber corta del Ad52 para su caracterización in vitro e in vivo como vector de terapia génica. [Thesis]. Universitat Autònoma de Barcelona; 2016. Available from: http://hdl.handle.net/10803/370116

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


University of South Florida

5. Ramachandran, Niraj. Corona Ion Deposition: A Novel Non-Contact Method for Drug and Gene Delivery to Living Systems.

Degree: 2008, University of South Florida

 Application of corona ions produced in air to B16F10 murine melanoma cells in vitro and in animal models resulted in the transport of molecular therapeutics… (more)

Subjects/Keywords: Plasma ions; Genetherapy; Electroporation; Molecular delivery; Tumors; American Studies; Arts and Humanities

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ramachandran, N. (2008). Corona Ion Deposition: A Novel Non-Contact Method for Drug and Gene Delivery to Living Systems. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/463

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):

Ramachandran, Niraj. “Corona Ion Deposition: A Novel Non-Contact Method for Drug and Gene Delivery to Living Systems.” 2008. Thesis, University of South Florida. Accessed September 23, 2020. https://scholarcommons.usf.edu/etd/463.

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

MLA Handbook (7th Edition):

Ramachandran, Niraj. “Corona Ion Deposition: A Novel Non-Contact Method for Drug and Gene Delivery to Living Systems.” 2008. Web. 23 Sep 2020.

Vancouver:

Ramachandran N. Corona Ion Deposition: A Novel Non-Contact Method for Drug and Gene Delivery to Living Systems. [Internet] [Thesis]. University of South Florida; 2008. [cited 2020 Sep 23]. Available from: https://scholarcommons.usf.edu/etd/463.

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

Council of Science Editors:

Ramachandran N. Corona Ion Deposition: A Novel Non-Contact Method for Drug and Gene Delivery to Living Systems. [Thesis]. University of South Florida; 2008. Available from: https://scholarcommons.usf.edu/etd/463

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

6. Rademaker, Hendrik Jan. Improvements in adenovirus-vector technology: aiming at replication specificity and vector integration.

Degree: 2007, Virus and Stem Cell Biology Group, Department of Molecular Cell Biology, Faculty of Medicine, Leiden University

 Current generation adenoviral vectors (Ads) are not suitable for those gene therapy approaches that require long-term gene expression. This is due to their high immunogenicity… (more)

Subjects/Keywords: Genetherapy; Adenovirus; Integration; Replication; Agrobacterium Tumefaciens; Bacteriophage Mu; CELO; PHELPS; OTE; Genetherapy; Adenovirus; Integration; Replication; Agrobacterium Tumefaciens; Bacteriophage Mu; CELO; PHELPS; OTE

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rademaker, H. J. (2007). Improvements in adenovirus-vector technology: aiming at replication specificity and vector integration. (Doctoral Dissertation). Virus and Stem Cell Biology Group, Department of Molecular Cell Biology, Faculty of Medicine, Leiden University. Retrieved from http://hdl.handle.net/1887/12039

Chicago Manual of Style (16th Edition):

Rademaker, Hendrik Jan. “Improvements in adenovirus-vector technology: aiming at replication specificity and vector integration.” 2007. Doctoral Dissertation, Virus and Stem Cell Biology Group, Department of Molecular Cell Biology, Faculty of Medicine, Leiden University. Accessed September 23, 2020. http://hdl.handle.net/1887/12039.

MLA Handbook (7th Edition):

Rademaker, Hendrik Jan. “Improvements in adenovirus-vector technology: aiming at replication specificity and vector integration.” 2007. Web. 23 Sep 2020.

Vancouver:

Rademaker HJ. Improvements in adenovirus-vector technology: aiming at replication specificity and vector integration. [Internet] [Doctoral dissertation]. Virus and Stem Cell Biology Group, Department of Molecular Cell Biology, Faculty of Medicine, Leiden University; 2007. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1887/12039.

Council of Science Editors:

Rademaker HJ. Improvements in adenovirus-vector technology: aiming at replication specificity and vector integration. [Doctoral Dissertation]. Virus and Stem Cell Biology Group, Department of Molecular Cell Biology, Faculty of Medicine, Leiden University; 2007. Available from: http://hdl.handle.net/1887/12039

7. Saccardo, Paolo. Development of artificial viruses for nanomedicine and gene therapy.

Degree: Departament de Genètica i de Microbiologia, 2015, Universitat Autònoma de Barcelona

 The convergence of different field as biotechnology, molecular biology and genetic engineering in the development of a nano-scale therapeutical vector became matter of interest because… (more)

Subjects/Keywords: Virus artificials; Virus artificiales; Artificial viruses; Teràpia gènica; Terapia génica; Genetherapy; Ciències Experimentals; 578

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Saccardo, P. (2015). Development of artificial viruses for nanomedicine and gene therapy. (Thesis). Universitat Autònoma de Barcelona. Retrieved from http://hdl.handle.net/10803/287907

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):

Saccardo, Paolo. “Development of artificial viruses for nanomedicine and gene therapy.” 2015. Thesis, Universitat Autònoma de Barcelona. Accessed September 23, 2020. http://hdl.handle.net/10803/287907.

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

MLA Handbook (7th Edition):

Saccardo, Paolo. “Development of artificial viruses for nanomedicine and gene therapy.” 2015. Web. 23 Sep 2020.

Vancouver:

Saccardo P. Development of artificial viruses for nanomedicine and gene therapy. [Internet] [Thesis]. Universitat Autònoma de Barcelona; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10803/287907.

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

Council of Science Editors:

Saccardo P. Development of artificial viruses for nanomedicine and gene therapy. [Thesis]. Universitat Autònoma de Barcelona; 2015. Available from: http://hdl.handle.net/10803/287907

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


University of Florida

8. Grimstein, Christian. Alpha-1 Antitrypsin Protein and Gene Therapies for the Prevention of Rheumatoid Arthritis in Mouse Models.

Degree: PhD, Pharmaceutical Sciences - Pharmacy, 2008, University of Florida

 Rheumatoid arthritis (RA) is an autoimmune disease characterized by immune cell infiltration, synovial hyperplasia, and progressive destruction of bone and cartilage, affecting about 1% of… (more)

Subjects/Keywords: Animal models; Antibodies; Arthritis; Autoantibodies; Control groups; Cytokines; Diseases; Gene therapy; Medical treatment; Rheumatoid arthritis; alpha1antitrypsin, arthritis, doxycycline, genetherapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Grimstein, C. (2008). Alpha-1 Antitrypsin Protein and Gene Therapies for the Prevention of Rheumatoid Arthritis in Mouse Models. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0023517

Chicago Manual of Style (16th Edition):

Grimstein, Christian. “Alpha-1 Antitrypsin Protein and Gene Therapies for the Prevention of Rheumatoid Arthritis in Mouse Models.” 2008. Doctoral Dissertation, University of Florida. Accessed September 23, 2020. https://ufdc.ufl.edu/UFE0023517.

MLA Handbook (7th Edition):

Grimstein, Christian. “Alpha-1 Antitrypsin Protein and Gene Therapies for the Prevention of Rheumatoid Arthritis in Mouse Models.” 2008. Web. 23 Sep 2020.

Vancouver:

Grimstein C. Alpha-1 Antitrypsin Protein and Gene Therapies for the Prevention of Rheumatoid Arthritis in Mouse Models. [Internet] [Doctoral dissertation]. University of Florida; 2008. [cited 2020 Sep 23]. Available from: https://ufdc.ufl.edu/UFE0023517.

Council of Science Editors:

Grimstein C. Alpha-1 Antitrypsin Protein and Gene Therapies for the Prevention of Rheumatoid Arthritis in Mouse Models. [Doctoral Dissertation]. University of Florida; 2008. Available from: https://ufdc.ufl.edu/UFE0023517


Freie Universität Berlin

9. Albers, Andreas. Development and characterization of a method for direct ballistic transfer of genes into tumor cells, for production of autologous anti-tumor vaccines.

Degree: 2002, Freie Universität Berlin

 The weak point of all gene therapy projects is still the gene transfer procedure. For clinical applications, a transfection method would be optimal, by which… (more)

Subjects/Keywords: genetherapy; zytokines; tumor vaccine; gene transfer; interleukin-7; GM-CSF; ballistic; transfection; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Albers, A. (2002). Development and characterization of a method for direct ballistic transfer of genes into tumor cells, for production of autologous anti-tumor vaccines. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-13694

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):

Albers, Andreas. “Development and characterization of a method for direct ballistic transfer of genes into tumor cells, for production of autologous anti-tumor vaccines.” 2002. Thesis, Freie Universität Berlin. Accessed September 23, 2020. http://dx.doi.org/10.17169/refubium-13694.

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

MLA Handbook (7th Edition):

Albers, Andreas. “Development and characterization of a method for direct ballistic transfer of genes into tumor cells, for production of autologous anti-tumor vaccines.” 2002. Web. 23 Sep 2020.

Vancouver:

Albers A. Development and characterization of a method for direct ballistic transfer of genes into tumor cells, for production of autologous anti-tumor vaccines. [Internet] [Thesis]. Freie Universität Berlin; 2002. [cited 2020 Sep 23]. Available from: http://dx.doi.org/10.17169/refubium-13694.

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

Council of Science Editors:

Albers A. Development and characterization of a method for direct ballistic transfer of genes into tumor cells, for production of autologous anti-tumor vaccines. [Thesis]. Freie Universität Berlin; 2002. Available from: http://dx.doi.org/10.17169/refubium-13694

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

10. Scalabrino, Miranda Leigh. Adeno Associated Viral Gene Therapy Targeting ON Bipolar Cells Restores Function in a Mouse Model of Congenital Stationary Night Blindness.

Degree: PhD, Medical Sciences - Genetics (IDP), 2016, University of Florida

 Adeno associated virus (AAV) effectively targets therapeutic genes to photoreceptors, pigment epithelia, Muller glia and ganglion cells of the retina. To date, no one has… (more)

Subjects/Keywords: Capsid; Gene therapy; Genetic mutation; Genomes; Night blindness; Photoreceptors; Retina; Sand sheets; Satellite viruses; Signals; aav  – csnb  – genetherapy  – nyctalopin  – retina

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Scalabrino, M. L. (2016). Adeno Associated Viral Gene Therapy Targeting ON Bipolar Cells Restores Function in a Mouse Model of Congenital Stationary Night Blindness. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0049771

Chicago Manual of Style (16th Edition):

Scalabrino, Miranda Leigh. “Adeno Associated Viral Gene Therapy Targeting ON Bipolar Cells Restores Function in a Mouse Model of Congenital Stationary Night Blindness.” 2016. Doctoral Dissertation, University of Florida. Accessed September 23, 2020. https://ufdc.ufl.edu/UFE0049771.

MLA Handbook (7th Edition):

Scalabrino, Miranda Leigh. “Adeno Associated Viral Gene Therapy Targeting ON Bipolar Cells Restores Function in a Mouse Model of Congenital Stationary Night Blindness.” 2016. Web. 23 Sep 2020.

Vancouver:

Scalabrino ML. Adeno Associated Viral Gene Therapy Targeting ON Bipolar Cells Restores Function in a Mouse Model of Congenital Stationary Night Blindness. [Internet] [Doctoral dissertation]. University of Florida; 2016. [cited 2020 Sep 23]. Available from: https://ufdc.ufl.edu/UFE0049771.

Council of Science Editors:

Scalabrino ML. Adeno Associated Viral Gene Therapy Targeting ON Bipolar Cells Restores Function in a Mouse Model of Congenital Stationary Night Blindness. [Doctoral Dissertation]. University of Florida; 2016. Available from: https://ufdc.ufl.edu/UFE0049771

.