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You searched for subject:(AAV). Showing records 1 – 30 of 191 total matches.

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1. Lostal, William. Approches thérapeutiques pour le traitement des dysferlinopathies : Therapeutical approaches for dysferlinopathies treatment.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2010, Evry-Val d'Essonne

Ce travail de thèse a porté sur le développement d'approches thérapeutiques pour les dysferlinopathies, pathologies dues à un déficit en dysferline, pour lesquelle sil n'existe… (more)

Subjects/Keywords: Aav

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

APA (6th Edition):

Lostal, W. (2010). Approches thérapeutiques pour le traitement des dysferlinopathies : Therapeutical approaches for dysferlinopathies treatment. (Doctoral Dissertation). Evry-Val d'Essonne. Retrieved from http://www.theses.fr/2010EVRY0009

Chicago Manual of Style (16th Edition):

Lostal, William. “Approches thérapeutiques pour le traitement des dysferlinopathies : Therapeutical approaches for dysferlinopathies treatment.” 2010. Doctoral Dissertation, Evry-Val d'Essonne. Accessed September 25, 2020. http://www.theses.fr/2010EVRY0009.

MLA Handbook (7th Edition):

Lostal, William. “Approches thérapeutiques pour le traitement des dysferlinopathies : Therapeutical approaches for dysferlinopathies treatment.” 2010. Web. 25 Sep 2020.

Vancouver:

Lostal W. Approches thérapeutiques pour le traitement des dysferlinopathies : Therapeutical approaches for dysferlinopathies treatment. [Internet] [Doctoral dissertation]. Evry-Val d'Essonne; 2010. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2010EVRY0009.

Council of Science Editors:

Lostal W. Approches thérapeutiques pour le traitement des dysferlinopathies : Therapeutical approaches for dysferlinopathies treatment. [Doctoral Dissertation]. Evry-Val d'Essonne; 2010. Available from: http://www.theses.fr/2010EVRY0009

2. Bello, Alexander Juanito Arquillano. Linking the tropism and transduction efficiency of porcine-derived adeno-associated viruses to their transgene-mediated protective efficacy.

Degree: Medical Microbiology, 2014, University of Manitoba

 Adeno-associated virus (AAV) is a small, non-pathogenic virus, exploited as a vector for gene therapy applications, with many successful clinical trials. However, these vectors are… (more)

Subjects/Keywords: AAV; Vaccine

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APA (6th Edition):

Bello, A. J. A. (2014). Linking the tropism and transduction efficiency of porcine-derived adeno-associated viruses to their transgene-mediated protective efficacy. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/23945

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):

Bello, Alexander Juanito Arquillano. “Linking the tropism and transduction efficiency of porcine-derived adeno-associated viruses to their transgene-mediated protective efficacy.” 2014. Thesis, University of Manitoba. Accessed September 25, 2020. http://hdl.handle.net/1993/23945.

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

MLA Handbook (7th Edition):

Bello, Alexander Juanito Arquillano. “Linking the tropism and transduction efficiency of porcine-derived adeno-associated viruses to their transgene-mediated protective efficacy.” 2014. Web. 25 Sep 2020.

Vancouver:

Bello AJA. Linking the tropism and transduction efficiency of porcine-derived adeno-associated viruses to their transgene-mediated protective efficacy. [Internet] [Thesis]. University of Manitoba; 2014. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/1993/23945.

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

Council of Science Editors:

Bello AJA. Linking the tropism and transduction efficiency of porcine-derived adeno-associated viruses to their transgene-mediated protective efficacy. [Thesis]. University of Manitoba; 2014. Available from: http://hdl.handle.net/1993/23945

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


University of Cambridge

3. Wong, Limy. The Genetics of Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis (AAV).

Degree: PhD, 2020, University of Cambridge

 Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a multi-systemic autoimmune disorder with evidence of circulating pathogenic ANCA. There are two main antigenic targets: proteinase 3… (more)

Subjects/Keywords: Genetics; AAV; GWAS

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

APA (6th Edition):

Wong, L. (2020). The Genetics of Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis (AAV). (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/303938

Chicago Manual of Style (16th Edition):

Wong, Limy. “The Genetics of Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis (AAV).” 2020. Doctoral Dissertation, University of Cambridge. Accessed September 25, 2020. https://www.repository.cam.ac.uk/handle/1810/303938.

MLA Handbook (7th Edition):

Wong, Limy. “The Genetics of Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis (AAV).” 2020. Web. 25 Sep 2020.

Vancouver:

Wong L. The Genetics of Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis (AAV). [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Sep 25]. Available from: https://www.repository.cam.ac.uk/handle/1810/303938.

Council of Science Editors:

Wong L. The Genetics of Anti-Neutrophil Cytoplasmic Antibody Associated Vasculitis (AAV). [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/303938


University of Cambridge

4. Wong, Limy. The genetics of anti-neutrophil cytoplasmic antibody associated vasculitis (AAV).

Degree: PhD, 2020, University of Cambridge

 Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a multi-systemic autoimmune disorder with evidence of circulating pathogenic ANCA. There are two main antigenic targets: proteinase 3… (more)

Subjects/Keywords: Genetics; AAV; GWAS

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

APA (6th Edition):

Wong, L. (2020). The genetics of anti-neutrophil cytoplasmic antibody associated vasculitis (AAV). (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/303938 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801925

Chicago Manual of Style (16th Edition):

Wong, Limy. “The genetics of anti-neutrophil cytoplasmic antibody associated vasculitis (AAV).” 2020. Doctoral Dissertation, University of Cambridge. Accessed September 25, 2020. https://www.repository.cam.ac.uk/handle/1810/303938 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801925.

MLA Handbook (7th Edition):

Wong, Limy. “The genetics of anti-neutrophil cytoplasmic antibody associated vasculitis (AAV).” 2020. Web. 25 Sep 2020.

Vancouver:

Wong L. The genetics of anti-neutrophil cytoplasmic antibody associated vasculitis (AAV). [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Sep 25]. Available from: https://www.repository.cam.ac.uk/handle/1810/303938 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801925.

Council of Science Editors:

Wong L. The genetics of anti-neutrophil cytoplasmic antibody associated vasculitis (AAV). [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/303938 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801925


Penn State University

5. Wang, Fan. Developing hippocampal delivery of AAV-NeuroD1 as a novel therapy for Alzheimer's disease.

Degree: 2016, Penn State University

 Alzheimer’s disease (AD) is the most common neurodegenerative disorder in the elderly and is the leading cause of most dementia cases. Patients with AD experience… (more)

Subjects/Keywords: Alzheimer's disease; NeuroD1; hippocampus; AAV

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

APA (6th Edition):

Wang, F. (2016). Developing hippocampal delivery of AAV-NeuroD1 as a novel therapy for Alzheimer's disease. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/27567

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, Fan. “Developing hippocampal delivery of AAV-NeuroD1 as a novel therapy for Alzheimer's disease.” 2016. Thesis, Penn State University. Accessed September 25, 2020. https://submit-etda.libraries.psu.edu/catalog/27567.

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

MLA Handbook (7th Edition):

Wang, Fan. “Developing hippocampal delivery of AAV-NeuroD1 as a novel therapy for Alzheimer's disease.” 2016. Web. 25 Sep 2020.

Vancouver:

Wang F. Developing hippocampal delivery of AAV-NeuroD1 as a novel therapy for Alzheimer's disease. [Internet] [Thesis]. Penn State University; 2016. [cited 2020 Sep 25]. Available from: https://submit-etda.libraries.psu.edu/catalog/27567.

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

Council of Science Editors:

Wang F. Developing hippocampal delivery of AAV-NeuroD1 as a novel therapy for Alzheimer's disease. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/27567

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


University of Rochester

6. Spahn, Jessica; Crispe, I. Nicholas. FasL and IFNy Effects on the CD8+ T cell Response to Hepatocellular Antigen.

Degree: PhD, 2011, University of Rochester

 Immune responses to hepatic pathogens often fail to elim invading organisms emphasizing the importance of understanding immune processes in the liver. CD8+ T cells are… (more)

Subjects/Keywords: Liver; Hepatitis; FasL; IFNy; AAV

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

APA (6th Edition):

Spahn, Jessica; Crispe, I. N. (2011). FasL and IFNy Effects on the CD8+ T cell Response to Hepatocellular Antigen. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/13981

Chicago Manual of Style (16th Edition):

Spahn, Jessica; Crispe, I Nicholas. “FasL and IFNy Effects on the CD8+ T cell Response to Hepatocellular Antigen.” 2011. Doctoral Dissertation, University of Rochester. Accessed September 25, 2020. http://hdl.handle.net/1802/13981.

MLA Handbook (7th Edition):

Spahn, Jessica; Crispe, I Nicholas. “FasL and IFNy Effects on the CD8+ T cell Response to Hepatocellular Antigen.” 2011. Web. 25 Sep 2020.

Vancouver:

Spahn, Jessica; Crispe IN. FasL and IFNy Effects on the CD8+ T cell Response to Hepatocellular Antigen. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/1802/13981.

Council of Science Editors:

Spahn, Jessica; Crispe IN. FasL and IFNy Effects on the CD8+ T cell Response to Hepatocellular Antigen. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/13981


Rice University

7. Lee, Esther Joy. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.

Degree: PhD, Bioengineering, 2018, Rice University

 Tissue engineering constitutes non-trivial processes that can be promoted through combinations of cells, materials and bioactive factors. The formation of tissues and organs demands spatiotemporal… (more)

Subjects/Keywords: AAV; gene delivery; tissue engineering

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

APA (6th Edition):

Lee, E. J. (2018). Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105809

Chicago Manual of Style (16th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Doctoral Dissertation, Rice University. Accessed September 25, 2020. http://hdl.handle.net/1911/105809.

MLA Handbook (7th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Web. 25 Sep 2020.

Vancouver:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/1911/105809.

Council of Science Editors:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105809


Rice University

8. Lee, Esther Joy. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.

Degree: PhD, Bioengineering, 2018, Rice University

 Tissue engineering constitutes non-trivial processes that can be promoted through combinations of cells, materials and bioactive factors. The formation of tissues and organs demands spatiotemporal… (more)

Subjects/Keywords: AAV; gene delivery; tissue engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lee, E. J. (2018). Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105810

Chicago Manual of Style (16th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Doctoral Dissertation, Rice University. Accessed September 25, 2020. http://hdl.handle.net/1911/105810.

MLA Handbook (7th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Web. 25 Sep 2020.

Vancouver:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/1911/105810.

Council of Science Editors:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105810


Rice University

9. Lee, Esther Joy. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.

Degree: PhD, Engineering, 2018, Rice University

 Tissue engineering constitutes non-trivial processes that can be promoted through combinations of cells, materials and bioactive factors. The formation of tissues and organs demands spatiotemporal… (more)

Subjects/Keywords: AAV; gene delivery; tissue engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lee, E. J. (2018). Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105807

Chicago Manual of Style (16th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Doctoral Dissertation, Rice University. Accessed September 25, 2020. http://hdl.handle.net/1911/105807.

MLA Handbook (7th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Web. 25 Sep 2020.

Vancouver:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/1911/105807.

Council of Science Editors:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105807


Rice University

10. Lee, Esther Joy. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.

Degree: PhD, Bioengineering, 2018, Rice University

 Tissue engineering constitutes non-trivial processes that can be promoted through combinations of cells, materials and bioactive factors. The formation of tissues and organs demands spatiotemporal… (more)

Subjects/Keywords: AAV; gene delivery; tissue engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lee, E. J. (2018). Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105808

Chicago Manual of Style (16th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Doctoral Dissertation, Rice University. Accessed September 25, 2020. http://hdl.handle.net/1911/105808.

MLA Handbook (7th Edition):

Lee, Esther Joy. “Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering.” 2018. Web. 25 Sep 2020.

Vancouver:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/1911/105808.

Council of Science Editors:

Lee EJ. Adeno-Associated Virus-Based Gene Delivery Approaches for Tissue Engineering. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105808


University of Florida

11. Huang, Lin-Ya. Engineering Improved Adeno-Associated Virus Vector Efficacy Guided by Capsid-Host Interactions.

Degree: PhD, Medical Sciences - Biochemistry and Molecular Biology (IDP), 2016, University of Florida

Subjects/Keywords: aav; parvovirus

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

APA (6th Edition):

Huang, L. (2016). Engineering Improved Adeno-Associated Virus Vector Efficacy Guided by Capsid-Host Interactions. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0050380

Chicago Manual of Style (16th Edition):

Huang, Lin-Ya. “Engineering Improved Adeno-Associated Virus Vector Efficacy Guided by Capsid-Host Interactions.” 2016. Doctoral Dissertation, University of Florida. Accessed September 25, 2020. https://ufdc.ufl.edu/UFE0050380.

MLA Handbook (7th Edition):

Huang, Lin-Ya. “Engineering Improved Adeno-Associated Virus Vector Efficacy Guided by Capsid-Host Interactions.” 2016. Web. 25 Sep 2020.

Vancouver:

Huang L. Engineering Improved Adeno-Associated Virus Vector Efficacy Guided by Capsid-Host Interactions. [Internet] [Doctoral dissertation]. University of Florida; 2016. [cited 2020 Sep 25]. Available from: https://ufdc.ufl.edu/UFE0050380.

Council of Science Editors:

Huang L. Engineering Improved Adeno-Associated Virus Vector Efficacy Guided by Capsid-Host Interactions. [Doctoral Dissertation]. University of Florida; 2016. Available from: https://ufdc.ufl.edu/UFE0050380


University of Florida

12. Lins, Bridget K. AAV Capsid Transitions in the Endolysosomal Pathway.

Degree: PhD, Medical Sciences - Biochemistry and Molecular Biology (IDP), 2015, University of Florida

Subjects/Keywords: aav; endolysosome

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APA (6th Edition):

Lins, B. K. (2015). AAV Capsid Transitions in the Endolysosomal Pathway. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0049109

Chicago Manual of Style (16th Edition):

Lins, Bridget K. “AAV Capsid Transitions in the Endolysosomal Pathway.” 2015. Doctoral Dissertation, University of Florida. Accessed September 25, 2020. https://ufdc.ufl.edu/UFE0049109.

MLA Handbook (7th Edition):

Lins, Bridget K. “AAV Capsid Transitions in the Endolysosomal Pathway.” 2015. Web. 25 Sep 2020.

Vancouver:

Lins BK. AAV Capsid Transitions in the Endolysosomal Pathway. [Internet] [Doctoral dissertation]. University of Florida; 2015. [cited 2020 Sep 25]. Available from: https://ufdc.ufl.edu/UFE0049109.

Council of Science Editors:

Lins BK. AAV Capsid Transitions in the Endolysosomal Pathway. [Doctoral Dissertation]. University of Florida; 2015. Available from: https://ufdc.ufl.edu/UFE0049109

13. Ameline, Baptiste. Evaluation du transfert d'optogènes pour le traitement par thérapie génique d'un modèle canin de dystrophies rétiniennes héréditaires. : Evaluation of optogene transfer for the treatment of a canine model of inherited retinal dystrophies.

Degree: Docteur es, Biomolécules pharmacologie thérapeutique, 2016, Nantes

La cécité ou la très grande malvoyance peut résulter de différentes pathologies comme les dystrophies rétiniennes héréditaires (DRH) caractérisées par la perte des photorécepteurs. Une… (more)

Subjects/Keywords: Optogénétique; AAV; ChR2; Opn4; Optogenetics; AAV; ChR2; Op4

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

APA (6th Edition):

Ameline, B. (2016). Evaluation du transfert d'optogènes pour le traitement par thérapie génique d'un modèle canin de dystrophies rétiniennes héréditaires. : Evaluation of optogene transfer for the treatment of a canine model of inherited retinal dystrophies. (Doctoral Dissertation). Nantes. Retrieved from http://www.theses.fr/2016NANT1001

Chicago Manual of Style (16th Edition):

Ameline, Baptiste. “Evaluation du transfert d'optogènes pour le traitement par thérapie génique d'un modèle canin de dystrophies rétiniennes héréditaires. : Evaluation of optogene transfer for the treatment of a canine model of inherited retinal dystrophies.” 2016. Doctoral Dissertation, Nantes. Accessed September 25, 2020. http://www.theses.fr/2016NANT1001.

MLA Handbook (7th Edition):

Ameline, Baptiste. “Evaluation du transfert d'optogènes pour le traitement par thérapie génique d'un modèle canin de dystrophies rétiniennes héréditaires. : Evaluation of optogene transfer for the treatment of a canine model of inherited retinal dystrophies.” 2016. Web. 25 Sep 2020.

Vancouver:

Ameline B. Evaluation du transfert d'optogènes pour le traitement par thérapie génique d'un modèle canin de dystrophies rétiniennes héréditaires. : Evaluation of optogene transfer for the treatment of a canine model of inherited retinal dystrophies. [Internet] [Doctoral dissertation]. Nantes; 2016. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2016NANT1001.

Council of Science Editors:

Ameline B. Evaluation du transfert d'optogènes pour le traitement par thérapie génique d'un modèle canin de dystrophies rétiniennes héréditaires. : Evaluation of optogene transfer for the treatment of a canine model of inherited retinal dystrophies. [Doctoral Dissertation]. Nantes; 2016. Available from: http://www.theses.fr/2016NANT1001


Temple University

14. Pokiniewski, Katie Ann. Understanding the cellular mechanism of Adeno-Associated Virus genome stabilization.

Degree: PhD, 2016, Temple University

Microbiology and Immunology

The Adeno-Associated Virus(AAV) is a small, single stranded DNA virus that has been developed as a gene transfer vector. Early clinical trials… (more)

Subjects/Keywords: Virology; Microbiology;

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

APA (6th Edition):

Pokiniewski, K. A. (2016). Understanding the cellular mechanism of Adeno-Associated Virus genome stabilization. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,385837

Chicago Manual of Style (16th Edition):

Pokiniewski, Katie Ann. “Understanding the cellular mechanism of Adeno-Associated Virus genome stabilization.” 2016. Doctoral Dissertation, Temple University. Accessed September 25, 2020. http://digital.library.temple.edu/u?/p245801coll10,385837.

MLA Handbook (7th Edition):

Pokiniewski, Katie Ann. “Understanding the cellular mechanism of Adeno-Associated Virus genome stabilization.” 2016. Web. 25 Sep 2020.

Vancouver:

Pokiniewski KA. Understanding the cellular mechanism of Adeno-Associated Virus genome stabilization. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2020 Sep 25]. Available from: http://digital.library.temple.edu/u?/p245801coll10,385837.

Council of Science Editors:

Pokiniewski KA. Understanding the cellular mechanism of Adeno-Associated Virus genome stabilization. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,385837


University of California – San Diego

15. Cheng, Yuhsiang. Development of a Novel Dual AAV System for Therapeutic Delivery of BDNF.

Degree: Biology, 2018, University of California – San Diego

 Alzheimer’s disease (AD) is a neurodegenerative disease that causes a reduction in brain-derived neurotrophic factor (BDNF) in multiple animal models, and delivery of BDNF provides… (more)

Subjects/Keywords: Neurosciences; AAV; Alzheimer's; BDNF; Gene; Regulatable; Therapy

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

APA (6th Edition):

Cheng, Y. (2018). Development of a Novel Dual AAV System for Therapeutic Delivery of BDNF. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/3v16w70m

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):

Cheng, Yuhsiang. “Development of a Novel Dual AAV System for Therapeutic Delivery of BDNF.” 2018. Thesis, University of California – San Diego. Accessed September 25, 2020. http://www.escholarship.org/uc/item/3v16w70m.

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

MLA Handbook (7th Edition):

Cheng, Yuhsiang. “Development of a Novel Dual AAV System for Therapeutic Delivery of BDNF.” 2018. Web. 25 Sep 2020.

Vancouver:

Cheng Y. Development of a Novel Dual AAV System for Therapeutic Delivery of BDNF. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Sep 25]. Available from: http://www.escholarship.org/uc/item/3v16w70m.

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

Council of Science Editors:

Cheng Y. Development of a Novel Dual AAV System for Therapeutic Delivery of BDNF. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/3v16w70m

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


The Ohio State University

16. Heller, Kristin Noreen. Alternative to Gene Replacement for Duchenne Muscular Dystrophy using Human Alpha7 Integrin (ITGA7).

Degree: PhD, Molecular, Cellular and Developmental Biology, 2014, The Ohio State University

 Duchenne Muscular Dystrophy (DMD) is a severe muscle disease caused by mutations in the dystrophin gene. Dystrophin helps link integral membrane proteins to the actin… (more)

Subjects/Keywords: Molecular Biology; AAV, DMD, ITGA7, Gene Therapy

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APA (6th Edition):

Heller, K. N. (2014). Alternative to Gene Replacement for Duchenne Muscular Dystrophy using Human Alpha7 Integrin (ITGA7). (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1388401639

Chicago Manual of Style (16th Edition):

Heller, Kristin Noreen. “Alternative to Gene Replacement for Duchenne Muscular Dystrophy using Human Alpha7 Integrin (ITGA7).” 2014. Doctoral Dissertation, The Ohio State University. Accessed September 25, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1388401639.

MLA Handbook (7th Edition):

Heller, Kristin Noreen. “Alternative to Gene Replacement for Duchenne Muscular Dystrophy using Human Alpha7 Integrin (ITGA7).” 2014. Web. 25 Sep 2020.

Vancouver:

Heller KN. Alternative to Gene Replacement for Duchenne Muscular Dystrophy using Human Alpha7 Integrin (ITGA7). [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Sep 25]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1388401639.

Council of Science Editors:

Heller KN. Alternative to Gene Replacement for Duchenne Muscular Dystrophy using Human Alpha7 Integrin (ITGA7). [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1388401639


Johannes Gutenberg Universität Mainz

17. Guggenhuber, Stephan. Targeting neuronal populations by AAV-mediated gene transfer for studying the endocannabinoid system.

Degree: 2013, Johannes Gutenberg Universität Mainz

 The cannabinoid type 1 (CB1) receptor is involved in a plethora of physiological functions and heterogeneously expressed on different neuronal populations. Several conditional loss-of-function studies… (more)

Subjects/Keywords: Neuroscience, Hippocampus, Endocannabinoid System, AAV; Life sciences

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APA (6th Edition):

Guggenhuber, S. (2013). Targeting neuronal populations by AAV-mediated gene transfer for studying the endocannabinoid system. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2015/4191/

Chicago Manual of Style (16th Edition):

Guggenhuber, Stephan. “Targeting neuronal populations by AAV-mediated gene transfer for studying the endocannabinoid system.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed September 25, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2015/4191/.

MLA Handbook (7th Edition):

Guggenhuber, Stephan. “Targeting neuronal populations by AAV-mediated gene transfer for studying the endocannabinoid system.” 2013. Web. 25 Sep 2020.

Vancouver:

Guggenhuber S. Targeting neuronal populations by AAV-mediated gene transfer for studying the endocannabinoid system. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2020 Sep 25]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4191/.

Council of Science Editors:

Guggenhuber S. Targeting neuronal populations by AAV-mediated gene transfer for studying the endocannabinoid system. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4191/


Colorado State University

18. Hemphill, Daniel. Development of an scAAVIGF-I gene therapeutic vector for the enhancement of cartilage repair.

Degree: PhD, Bioengineering, 2014, Colorado State University

 In this work, we hypothesize scAAVIGF-I can be efficiently engineered and used as a gene therapeutic vector to transduce cartilage and synovium and elicit biochemical… (more)

Subjects/Keywords: cartilage; AAV; gene therapy; IGF-I

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APA (6th Edition):

Hemphill, D. (2014). Development of an scAAVIGF-I gene therapeutic vector for the enhancement of cartilage repair. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/83777

Chicago Manual of Style (16th Edition):

Hemphill, Daniel. “Development of an scAAVIGF-I gene therapeutic vector for the enhancement of cartilage repair.” 2014. Doctoral Dissertation, Colorado State University. Accessed September 25, 2020. http://hdl.handle.net/10217/83777.

MLA Handbook (7th Edition):

Hemphill, Daniel. “Development of an scAAVIGF-I gene therapeutic vector for the enhancement of cartilage repair.” 2014. Web. 25 Sep 2020.

Vancouver:

Hemphill D. Development of an scAAVIGF-I gene therapeutic vector for the enhancement of cartilage repair. [Internet] [Doctoral dissertation]. Colorado State University; 2014. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/10217/83777.

Council of Science Editors:

Hemphill D. Development of an scAAVIGF-I gene therapeutic vector for the enhancement of cartilage repair. [Doctoral Dissertation]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/83777


Boston College

19. Rockwell, Hannah. AAV-Mediated Gene Delivery Corrects CNS Lysosomal Storage in Cats with Juvenile Sandhoff Disease.

Degree: MS, Biology, 2013, Boston College

 Sandhoff Disease (SD) is an autosomal recessive neurodegenerative disease caused by a mutation in the Hexb gene for the β-subunit of β-hexosaminidase A, resulting in… (more)

Subjects/Keywords: AAV; Cat; Cerebroside; GM2; Sandhoff Disease; Sulfatide

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APA (6th Edition):

Rockwell, H. (2013). AAV-Mediated Gene Delivery Corrects CNS Lysosomal Storage in Cats with Juvenile Sandhoff Disease. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101484

Chicago Manual of Style (16th Edition):

Rockwell, Hannah. “AAV-Mediated Gene Delivery Corrects CNS Lysosomal Storage in Cats with Juvenile Sandhoff Disease.” 2013. Masters Thesis, Boston College. Accessed September 25, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101484.

MLA Handbook (7th Edition):

Rockwell, Hannah. “AAV-Mediated Gene Delivery Corrects CNS Lysosomal Storage in Cats with Juvenile Sandhoff Disease.” 2013. Web. 25 Sep 2020.

Vancouver:

Rockwell H. AAV-Mediated Gene Delivery Corrects CNS Lysosomal Storage in Cats with Juvenile Sandhoff Disease. [Internet] [Masters thesis]. Boston College; 2013. [cited 2020 Sep 25]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101484.

Council of Science Editors:

Rockwell H. AAV-Mediated Gene Delivery Corrects CNS Lysosomal Storage in Cats with Juvenile Sandhoff Disease. [Masters Thesis]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101484


Victoria University of Wellington

20. Belhoul-Fakir, Hanane. Construction and optimization of novel recombinant Adeno-Associated Virus rAAV2/5 for targeting microglia to regulate immune responses during neuroinflammation.

Degree: 2014, Victoria University of Wellington

 Activated microglia promote central nervous system (CNS) inflammation through antigen presentation and secretion of pro-inflammatory cytokines and chemokines. Although this activation is necessary to protect… (more)

Subjects/Keywords: AAV; Adeno-Associated Virus; Microglia; Neuro-inflammation

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APA (6th Edition):

Belhoul-Fakir, H. (2014). Construction and optimization of novel recombinant Adeno-Associated Virus rAAV2/5 for targeting microglia to regulate immune responses during neuroinflammation. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/3650

Chicago Manual of Style (16th Edition):

Belhoul-Fakir, Hanane. “Construction and optimization of novel recombinant Adeno-Associated Virus rAAV2/5 for targeting microglia to regulate immune responses during neuroinflammation.” 2014. Masters Thesis, Victoria University of Wellington. Accessed September 25, 2020. http://hdl.handle.net/10063/3650.

MLA Handbook (7th Edition):

Belhoul-Fakir, Hanane. “Construction and optimization of novel recombinant Adeno-Associated Virus rAAV2/5 for targeting microglia to regulate immune responses during neuroinflammation.” 2014. Web. 25 Sep 2020.

Vancouver:

Belhoul-Fakir H. Construction and optimization of novel recombinant Adeno-Associated Virus rAAV2/5 for targeting microglia to regulate immune responses during neuroinflammation. [Internet] [Masters thesis]. Victoria University of Wellington; 2014. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/10063/3650.

Council of Science Editors:

Belhoul-Fakir H. Construction and optimization of novel recombinant Adeno-Associated Virus rAAV2/5 for targeting microglia to regulate immune responses during neuroinflammation. [Masters Thesis]. Victoria University of Wellington; 2014. Available from: http://hdl.handle.net/10063/3650

21. P. Tornabene. LARGE GENE DELIVERY TO THE RETINA BY MULTIPLE AAV VECTORS.

Degree: 2019, Università degli Studi di Milano

 Retinal gene therapy with adeno-associated viral (AAV) vectors is safe and effective yet it is limited by AAV cargo capacity of about 5 kb. AAV(more)

Subjects/Keywords: AAV, retinal gene therapy, triple AAV vectors, protein trans-splicing; Settore BIO/18 - Genetica

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APA (6th Edition):

Tornabene, P. (2019). LARGE GENE DELIVERY TO THE RETINA BY MULTIPLE AAV VECTORS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/608611

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):

Tornabene, P.. “LARGE GENE DELIVERY TO THE RETINA BY MULTIPLE AAV VECTORS.” 2019. Thesis, Università degli Studi di Milano. Accessed September 25, 2020. http://hdl.handle.net/2434/608611.

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

MLA Handbook (7th Edition):

Tornabene, P.. “LARGE GENE DELIVERY TO THE RETINA BY MULTIPLE AAV VECTORS.” 2019. Web. 25 Sep 2020.

Vancouver:

Tornabene P. LARGE GENE DELIVERY TO THE RETINA BY MULTIPLE AAV VECTORS. [Internet] [Thesis]. Università degli Studi di Milano; 2019. [cited 2020 Sep 25]. Available from: http://hdl.handle.net/2434/608611.

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

Council of Science Editors:

Tornabene P. LARGE GENE DELIVERY TO THE RETINA BY MULTIPLE AAV VECTORS. [Thesis]. Università degli Studi di Milano; 2019. Available from: http://hdl.handle.net/2434/608611

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


Uppsala University

22. Eriksson, Elin. Development and comparison of three immunoassay formats to screen for total anti-adeno-associated virus serotype 2 antibodies in human serum using the Gyrolab immunoassay platform.

Degree: Biology Education Centre, 2020, Uppsala University

  Recombinant adeno-associated virus vectors are one of the most promising gene delivery tools for applications within gene- and cell therapy. The high level of… (more)

Subjects/Keywords: Adeno-associated virus; AAV; anti-AAV; TAb; Gyrolab; immunity; immunoassay; Immunology; Immunologi

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APA (6th Edition):

Eriksson, E. (2020). Development and comparison of three immunoassay formats to screen for total anti-adeno-associated virus serotype 2 antibodies in human serum using the Gyrolab immunoassay platform. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413055

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):

Eriksson, Elin. “Development and comparison of three immunoassay formats to screen for total anti-adeno-associated virus serotype 2 antibodies in human serum using the Gyrolab immunoassay platform.” 2020. Thesis, Uppsala University. Accessed September 25, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413055.

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

MLA Handbook (7th Edition):

Eriksson, Elin. “Development and comparison of three immunoassay formats to screen for total anti-adeno-associated virus serotype 2 antibodies in human serum using the Gyrolab immunoassay platform.” 2020. Web. 25 Sep 2020.

Vancouver:

Eriksson E. Development and comparison of three immunoassay formats to screen for total anti-adeno-associated virus serotype 2 antibodies in human serum using the Gyrolab immunoassay platform. [Internet] [Thesis]. Uppsala University; 2020. [cited 2020 Sep 25]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413055.

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

Council of Science Editors:

Eriksson E. Development and comparison of three immunoassay formats to screen for total anti-adeno-associated virus serotype 2 antibodies in human serum using the Gyrolab immunoassay platform. [Thesis]. Uppsala University; 2020. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-413055

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

23. Wein, Nicolas. Nouveaux outils exploratoires et développement d'approches thérapeutiques dans les dysferlinopathies primaires : Development of novel diagnosis tools and exploration of innovative therapeutic approaches in primary dysferlinopathies.

Degree: Docteur es, Pathologie humaine, 2010, Aix-Marseille 2

Les dysferlinopathies constituent un groupe de dystrophies musculaires autosomiques récessives comprenantprincipalement la myopathie des ceintures (LGMD) de type 2B et la myopathie distale de Miyoshi.… (more)

Subjects/Keywords: Dysferline; Réparation membranaire; Saut d'exon; Miniprotéine; Aav; Cgh; Muscle; Dysferlinopathies; AAV gene transfer

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APA (6th Edition):

Wein, N. (2010). Nouveaux outils exploratoires et développement d'approches thérapeutiques dans les dysferlinopathies primaires : Development of novel diagnosis tools and exploration of innovative therapeutic approaches in primary dysferlinopathies. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX20704

Chicago Manual of Style (16th Edition):

Wein, Nicolas. “Nouveaux outils exploratoires et développement d'approches thérapeutiques dans les dysferlinopathies primaires : Development of novel diagnosis tools and exploration of innovative therapeutic approaches in primary dysferlinopathies.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed September 25, 2020. http://www.theses.fr/2010AIX20704.

MLA Handbook (7th Edition):

Wein, Nicolas. “Nouveaux outils exploratoires et développement d'approches thérapeutiques dans les dysferlinopathies primaires : Development of novel diagnosis tools and exploration of innovative therapeutic approaches in primary dysferlinopathies.” 2010. Web. 25 Sep 2020.

Vancouver:

Wein N. Nouveaux outils exploratoires et développement d'approches thérapeutiques dans les dysferlinopathies primaires : Development of novel diagnosis tools and exploration of innovative therapeutic approaches in primary dysferlinopathies. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2010AIX20704.

Council of Science Editors:

Wein N. Nouveaux outils exploratoires et développement d'approches thérapeutiques dans les dysferlinopathies primaires : Development of novel diagnosis tools and exploration of innovative therapeutic approaches in primary dysferlinopathies. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX20704

24. Meliani, Amine. Prevention and inhibition of adverse humoral immune response to gene therapy mediated by adeno-associated virus (AAV) vector : Prévention et inhibition de la réponse immune humorale indésirable à la thérapie génique médiée par le vecteur viral adéno-associés (AAV).

Degree: Docteur es, Immunologie, 2018, Sorbonne université

La thérapie génique peut être définie comme le transfert du gène thérapeutique dans le tissue d’intérêt à l’aide d’un vecteur. A ce jour, les vecteurs… (more)

Subjects/Keywords: AAV; Thérapie génique; Réponse immunitaire; Anticorps; Prévention; Tolérance; AAV; Gene therapy; Immune response; 615.37

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APA (6th Edition):

Meliani, A. (2018). Prevention and inhibition of adverse humoral immune response to gene therapy mediated by adeno-associated virus (AAV) vector : Prévention et inhibition de la réponse immune humorale indésirable à la thérapie génique médiée par le vecteur viral adéno-associés (AAV). (Doctoral Dissertation). Sorbonne université. Retrieved from http://www.theses.fr/2018SORUS051

Chicago Manual of Style (16th Edition):

Meliani, Amine. “Prevention and inhibition of adverse humoral immune response to gene therapy mediated by adeno-associated virus (AAV) vector : Prévention et inhibition de la réponse immune humorale indésirable à la thérapie génique médiée par le vecteur viral adéno-associés (AAV).” 2018. Doctoral Dissertation, Sorbonne université. Accessed September 25, 2020. http://www.theses.fr/2018SORUS051.

MLA Handbook (7th Edition):

Meliani, Amine. “Prevention and inhibition of adverse humoral immune response to gene therapy mediated by adeno-associated virus (AAV) vector : Prévention et inhibition de la réponse immune humorale indésirable à la thérapie génique médiée par le vecteur viral adéno-associés (AAV).” 2018. Web. 25 Sep 2020.

Vancouver:

Meliani A. Prevention and inhibition of adverse humoral immune response to gene therapy mediated by adeno-associated virus (AAV) vector : Prévention et inhibition de la réponse immune humorale indésirable à la thérapie génique médiée par le vecteur viral adéno-associés (AAV). [Internet] [Doctoral dissertation]. Sorbonne université; 2018. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2018SORUS051.

Council of Science Editors:

Meliani A. Prevention and inhibition of adverse humoral immune response to gene therapy mediated by adeno-associated virus (AAV) vector : Prévention et inhibition de la réponse immune humorale indésirable à la thérapie génique médiée par le vecteur viral adéno-associés (AAV). [Doctoral Dissertation]. Sorbonne université; 2018. Available from: http://www.theses.fr/2018SORUS051

25. Perdomini, Morgane. Développement d'une thérapie génique dans le modèle murin cardiaque de l'ataxie de Friedreich en utilisant le vecteur adéno-associé rAAVrh10 : Development of a gene therapy approach in a cardiac mouse model of Friedreich ataxia using a recombinant adeno-associated vector rAAVrh10.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Université de Strasbourg

L’ataxie de Friedreich (AF) est une maladie mitochondriale caractérisée par une ataxie spinocérébelleuse et sensitive, une cardiomyopathie et un diabète. L’AF est due à un… (more)

Subjects/Keywords: Ataxie de Friedreich; Thérapie génique; AAV; Cardiomyopathie; Freidreich ataxia; Gene therapy; AAV; Cardiomyopathie; 572.4; 572.8; 616

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APA (6th Edition):

Perdomini, M. (2013). Développement d'une thérapie génique dans le modèle murin cardiaque de l'ataxie de Friedreich en utilisant le vecteur adéno-associé rAAVrh10 : Development of a gene therapy approach in a cardiac mouse model of Friedreich ataxia using a recombinant adeno-associated vector rAAVrh10. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2013STRAJ105

Chicago Manual of Style (16th Edition):

Perdomini, Morgane. “Développement d'une thérapie génique dans le modèle murin cardiaque de l'ataxie de Friedreich en utilisant le vecteur adéno-associé rAAVrh10 : Development of a gene therapy approach in a cardiac mouse model of Friedreich ataxia using a recombinant adeno-associated vector rAAVrh10.” 2013. Doctoral Dissertation, Université de Strasbourg. Accessed September 25, 2020. http://www.theses.fr/2013STRAJ105.

MLA Handbook (7th Edition):

Perdomini, Morgane. “Développement d'une thérapie génique dans le modèle murin cardiaque de l'ataxie de Friedreich en utilisant le vecteur adéno-associé rAAVrh10 : Development of a gene therapy approach in a cardiac mouse model of Friedreich ataxia using a recombinant adeno-associated vector rAAVrh10.” 2013. Web. 25 Sep 2020.

Vancouver:

Perdomini M. Développement d'une thérapie génique dans le modèle murin cardiaque de l'ataxie de Friedreich en utilisant le vecteur adéno-associé rAAVrh10 : Development of a gene therapy approach in a cardiac mouse model of Friedreich ataxia using a recombinant adeno-associated vector rAAVrh10. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2013. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2013STRAJ105.

Council of Science Editors:

Perdomini M. Développement d'une thérapie génique dans le modèle murin cardiaque de l'ataxie de Friedreich en utilisant le vecteur adéno-associé rAAVrh10 : Development of a gene therapy approach in a cardiac mouse model of Friedreich ataxia using a recombinant adeno-associated vector rAAVrh10. [Doctoral Dissertation]. Université de Strasbourg; 2013. Available from: http://www.theses.fr/2013STRAJ105

26. Valencia Garcia, Sara. Décryptage du réseau neuronal responsable de l’atonie musculaire pendant le sommeil paradoxal chez le rat : création d’un modèle rongeur du RBD (REM sleep Behavior Disorder) : Neuronal network of paradoxical sleep muscle atonia : a pre-requirement in the creation of a RBD (REM sleep Behavior Disorder) rodent model.

Degree: Docteur es, Neurosciences, 2014, Université Claude Bernard – Lyon I

Les circuits neuronaux responsables du sommeil paradoxal (SP) et de l'atonie musculaire qui le caractéristique sont l'objet de nombreuses recherches expérimentales, notamment en raison de… (more)

Subjects/Keywords: Tronc cérébral; C-Fos; Glutamate; Glycine; AAV-shRNA; Motoneurones somatiques; Brainstem; C-Fos; Glutamate; Glycine; AAV-shRNA; Somatic motoneurons; 612.8

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APA (6th Edition):

Valencia Garcia, S. (2014). Décryptage du réseau neuronal responsable de l’atonie musculaire pendant le sommeil paradoxal chez le rat : création d’un modèle rongeur du RBD (REM sleep Behavior Disorder) : Neuronal network of paradoxical sleep muscle atonia : a pre-requirement in the creation of a RBD (REM sleep Behavior Disorder) rodent model. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2014LYO10324

Chicago Manual of Style (16th Edition):

Valencia Garcia, Sara. “Décryptage du réseau neuronal responsable de l’atonie musculaire pendant le sommeil paradoxal chez le rat : création d’un modèle rongeur du RBD (REM sleep Behavior Disorder) : Neuronal network of paradoxical sleep muscle atonia : a pre-requirement in the creation of a RBD (REM sleep Behavior Disorder) rodent model.” 2014. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed September 25, 2020. http://www.theses.fr/2014LYO10324.

MLA Handbook (7th Edition):

Valencia Garcia, Sara. “Décryptage du réseau neuronal responsable de l’atonie musculaire pendant le sommeil paradoxal chez le rat : création d’un modèle rongeur du RBD (REM sleep Behavior Disorder) : Neuronal network of paradoxical sleep muscle atonia : a pre-requirement in the creation of a RBD (REM sleep Behavior Disorder) rodent model.” 2014. Web. 25 Sep 2020.

Vancouver:

Valencia Garcia S. Décryptage du réseau neuronal responsable de l’atonie musculaire pendant le sommeil paradoxal chez le rat : création d’un modèle rongeur du RBD (REM sleep Behavior Disorder) : Neuronal network of paradoxical sleep muscle atonia : a pre-requirement in the creation of a RBD (REM sleep Behavior Disorder) rodent model. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2014. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2014LYO10324.

Council of Science Editors:

Valencia Garcia S. Décryptage du réseau neuronal responsable de l’atonie musculaire pendant le sommeil paradoxal chez le rat : création d’un modèle rongeur du RBD (REM sleep Behavior Disorder) : Neuronal network of paradoxical sleep muscle atonia : a pre-requirement in the creation of a RBD (REM sleep Behavior Disorder) rodent model. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2014. Available from: http://www.theses.fr/2014LYO10324

27. Ploquin, Aurélie. Les vecteurs AAV recombinants : un nouvel outil de vaccination contre les Hénipavirus : Recombinant AAV vectors : a new vaccination tool against Henipaviruses.

Degree: Docteur es, Sciences de la vie, 2012, Lyon, École normale supérieure

Les virus Hendra (HeV) et Nipah (NiV) sont des virus émergents appartenant à la famille des Paramyxovirus et au genre des Hénipavirus. Chaque année, ils… (more)

Subjects/Keywords: Hénipavirus; Vaccination; Vecteur AAV; Anticorps neutralisants; Glycoprotéine G; Henipavirus; Vaccination; AAV vectors; Neutralising antibodies; G glycoprotein

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APA (6th Edition):

Ploquin, A. (2012). Les vecteurs AAV recombinants : un nouvel outil de vaccination contre les Hénipavirus : Recombinant AAV vectors : a new vaccination tool against Henipaviruses. (Doctoral Dissertation). Lyon, École normale supérieure. Retrieved from http://www.theses.fr/2012ENSL0739

Chicago Manual of Style (16th Edition):

Ploquin, Aurélie. “Les vecteurs AAV recombinants : un nouvel outil de vaccination contre les Hénipavirus : Recombinant AAV vectors : a new vaccination tool against Henipaviruses.” 2012. Doctoral Dissertation, Lyon, École normale supérieure. Accessed September 25, 2020. http://www.theses.fr/2012ENSL0739.

MLA Handbook (7th Edition):

Ploquin, Aurélie. “Les vecteurs AAV recombinants : un nouvel outil de vaccination contre les Hénipavirus : Recombinant AAV vectors : a new vaccination tool against Henipaviruses.” 2012. Web. 25 Sep 2020.

Vancouver:

Ploquin A. Les vecteurs AAV recombinants : un nouvel outil de vaccination contre les Hénipavirus : Recombinant AAV vectors : a new vaccination tool against Henipaviruses. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; 2012. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2012ENSL0739.

Council of Science Editors:

Ploquin A. Les vecteurs AAV recombinants : un nouvel outil de vaccination contre les Hénipavirus : Recombinant AAV vectors : a new vaccination tool against Henipaviruses. [Doctoral Dissertation]. Lyon, École normale supérieure; 2012. Available from: http://www.theses.fr/2012ENSL0739

28. De Montigny, Charline. Compréhension de la neurophysiopathologie de l'ataxie de Friedreich et développement d'une approche de thérapie génique dans un nouveau modèle murin : Understanding Friedreich’s ataxia neuropathophysiology and development of a gene therapy approach using a new mouse model.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2018, Université de Strasbourg

L’ataxie de Friedreich (AF) est une maladie mitochondriale caractérisée par une ataxie sensitive et spinocérébelleuse, une cardiomyopathie et du diabète, pour laquelle il n’existe pas… (more)

Subjects/Keywords: Ataxie de Friedreich; Neurophysiopathologie; Neurones proprioceptifs; Thérapie génique; AAV; Friedreich ataxia; Neuropathophysiology; Proprioceptive neurons; Gene therapy; AAV; 572.8; 616.042

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APA (6th Edition):

De Montigny, C. (2018). Compréhension de la neurophysiopathologie de l'ataxie de Friedreich et développement d'une approche de thérapie génique dans un nouveau modèle murin : Understanding Friedreich’s ataxia neuropathophysiology and development of a gene therapy approach using a new mouse model. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAJ051

Chicago Manual of Style (16th Edition):

De Montigny, Charline. “Compréhension de la neurophysiopathologie de l'ataxie de Friedreich et développement d'une approche de thérapie génique dans un nouveau modèle murin : Understanding Friedreich’s ataxia neuropathophysiology and development of a gene therapy approach using a new mouse model.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed September 25, 2020. http://www.theses.fr/2018STRAJ051.

MLA Handbook (7th Edition):

De Montigny, Charline. “Compréhension de la neurophysiopathologie de l'ataxie de Friedreich et développement d'une approche de thérapie génique dans un nouveau modèle murin : Understanding Friedreich’s ataxia neuropathophysiology and development of a gene therapy approach using a new mouse model.” 2018. Web. 25 Sep 2020.

Vancouver:

De Montigny C. Compréhension de la neurophysiopathologie de l'ataxie de Friedreich et développement d'une approche de thérapie génique dans un nouveau modèle murin : Understanding Friedreich’s ataxia neuropathophysiology and development of a gene therapy approach using a new mouse model. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2018STRAJ051.

Council of Science Editors:

De Montigny C. Compréhension de la neurophysiopathologie de l'ataxie de Friedreich et développement d'une approche de thérapie génique dans un nouveau modèle murin : Understanding Friedreich’s ataxia neuropathophysiology and development of a gene therapy approach using a new mouse model. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAJ051

29. Dias Florencio Leite, Gabriella. Recombinant Adeno-Associated Viruses : process development and gene transfer application for muscular dystrophy : Virus recombinant associés à l'adénovirus : développement des procédés et application du transfert de gène pour la dystrophie musculaire.

Degree: Docteur es, Physiologie, physiopathologie, 2017, Université Paris-Saclay (ComUE)

L'intérêt de l’utilisation des vecteurs viraux comme le Adeno-Associated Virus recombinant (rAAV) dans la recherche pour le traitement des maladies génétiques a conduit à une… (more)

Subjects/Keywords: Dystrophie musculaire de Duchenne; Thérapie génique; AAV; CRISPR-Cas9; Duchenne muscular distrophy; Gene therapy; AAV; CRISPR-Cas9

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

APA (6th Edition):

Dias Florencio Leite, G. (2017). Recombinant Adeno-Associated Viruses : process development and gene transfer application for muscular dystrophy : Virus recombinant associés à l'adénovirus : développement des procédés et application du transfert de gène pour la dystrophie musculaire. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLV051

Chicago Manual of Style (16th Edition):

Dias Florencio Leite, Gabriella. “Recombinant Adeno-Associated Viruses : process development and gene transfer application for muscular dystrophy : Virus recombinant associés à l'adénovirus : développement des procédés et application du transfert de gène pour la dystrophie musculaire.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed September 25, 2020. http://www.theses.fr/2017SACLV051.

MLA Handbook (7th Edition):

Dias Florencio Leite, Gabriella. “Recombinant Adeno-Associated Viruses : process development and gene transfer application for muscular dystrophy : Virus recombinant associés à l'adénovirus : développement des procédés et application du transfert de gène pour la dystrophie musculaire.” 2017. Web. 25 Sep 2020.

Vancouver:

Dias Florencio Leite G. Recombinant Adeno-Associated Viruses : process development and gene transfer application for muscular dystrophy : Virus recombinant associés à l'adénovirus : développement des procédés et application du transfert de gène pour la dystrophie musculaire. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2017SACLV051.

Council of Science Editors:

Dias Florencio Leite G. Recombinant Adeno-Associated Viruses : process development and gene transfer application for muscular dystrophy : Virus recombinant associés à l'adénovirus : développement des procédés et application du transfert de gène pour la dystrophie musculaire. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLV051

30. Planul, Arthur. Evolution dirigée de virus adéno-associés pour un transfert de gène efficace dans le système visuel : Directed evolution of adeno-associated viruses for efficient gene transfer in the visual system.

Degree: Docteur es, Neurosciences, 2017, Université Pierre et Marie Curie – Paris VI

Les virus adéno-associés (AAVs) font partie des vecteurs les plus efficaces pour le transfert de gène, en particulier dans la rétine. Ils sont utilisés aussi… (more)

Subjects/Keywords: AAV; Evolution dirigée; Vecteurs; Transport axonal; Transfert de gène; Rétine humaine; AAV; Directed evolution; Human retina; 612.84

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

APA (6th Edition):

Planul, A. (2017). Evolution dirigée de virus adéno-associés pour un transfert de gène efficace dans le système visuel : Directed evolution of adeno-associated viruses for efficient gene transfer in the visual system. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2017PA066344

Chicago Manual of Style (16th Edition):

Planul, Arthur. “Evolution dirigée de virus adéno-associés pour un transfert de gène efficace dans le système visuel : Directed evolution of adeno-associated viruses for efficient gene transfer in the visual system.” 2017. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed September 25, 2020. http://www.theses.fr/2017PA066344.

MLA Handbook (7th Edition):

Planul, Arthur. “Evolution dirigée de virus adéno-associés pour un transfert de gène efficace dans le système visuel : Directed evolution of adeno-associated viruses for efficient gene transfer in the visual system.” 2017. Web. 25 Sep 2020.

Vancouver:

Planul A. Evolution dirigée de virus adéno-associés pour un transfert de gène efficace dans le système visuel : Directed evolution of adeno-associated viruses for efficient gene transfer in the visual system. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. [cited 2020 Sep 25]. Available from: http://www.theses.fr/2017PA066344.

Council of Science Editors:

Planul A. Evolution dirigée de virus adéno-associés pour un transfert de gène efficace dans le système visuel : Directed evolution of adeno-associated viruses for efficient gene transfer in the visual system. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2017. Available from: http://www.theses.fr/2017PA066344

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