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You searched for subject:( Lentivirus). Showing records 1 – 30 of 133 total matches.

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University of Texas Southwestern Medical Center

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

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 March 07, 2021. 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 Mar 2021.

Vancouver:

Ellis BL. Improving Viral Vectors for Gene Targeting in Gene Therapy. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2021 Mar 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


University of Adelaide

2. 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 March 07, 2021. 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 Mar 2021.

Vancouver:

Kremer KL. Cystic Fibrosis gene therapy: methods for the optimisation of CFTR gene delivery. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2021 Mar 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


Victoria University of Wellington

3. Upton, Jevon. Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes.

Degree: 2020, Victoria University of Wellington

 Developing transgenic livestock has become popular in recent years after advances in the field of genetic editing. Cattle are one of the main exports in… (more)

Subjects/Keywords: CRISPR/Cas9; Bovine Embryology; Lentivirus

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APA (6th Edition):

Upton, J. (2020). Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8944

Chicago Manual of Style (16th Edition):

Upton, Jevon. “Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes.” 2020. Masters Thesis, Victoria University of Wellington. Accessed March 07, 2021. http://hdl.handle.net/10063/8944.

MLA Handbook (7th Edition):

Upton, Jevon. “Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes.” 2020. Web. 07 Mar 2021.

Vancouver:

Upton J. Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes. [Internet] [Masters thesis]. Victoria University of Wellington; 2020. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10063/8944.

Council of Science Editors:

Upton J. Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes. [Masters Thesis]. Victoria University of Wellington; 2020. Available from: http://hdl.handle.net/10063/8944


Victoria University of Wellington

4. Ni, Shicheng. Adapting CRISPR/Cas9 Lentivirus Technology for Functional Studies of GATA6 & GATA4 during Bovine Preimplantation Embryogenesis.

Degree: 2020, Victoria University of Wellington

 In recent times, cattle embryology has been under the spotlight of investigation due to its apparent economic values. This is especially relevant in the case… (more)

Subjects/Keywords: CRISPR; Bovine Embryology; Lentivirus

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APA (6th Edition):

Ni, S. (2020). Adapting CRISPR/Cas9 Lentivirus Technology for Functional Studies of GATA6 & GATA4 during Bovine Preimplantation Embryogenesis. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8989

Chicago Manual of Style (16th Edition):

Ni, Shicheng. “Adapting CRISPR/Cas9 Lentivirus Technology for Functional Studies of GATA6 & GATA4 during Bovine Preimplantation Embryogenesis.” 2020. Masters Thesis, Victoria University of Wellington. Accessed March 07, 2021. http://hdl.handle.net/10063/8989.

MLA Handbook (7th Edition):

Ni, Shicheng. “Adapting CRISPR/Cas9 Lentivirus Technology for Functional Studies of GATA6 & GATA4 during Bovine Preimplantation Embryogenesis.” 2020. Web. 07 Mar 2021.

Vancouver:

Ni S. Adapting CRISPR/Cas9 Lentivirus Technology for Functional Studies of GATA6 & GATA4 during Bovine Preimplantation Embryogenesis. [Internet] [Masters thesis]. Victoria University of Wellington; 2020. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10063/8989.

Council of Science Editors:

Ni S. Adapting CRISPR/Cas9 Lentivirus Technology for Functional Studies of GATA6 & GATA4 during Bovine Preimplantation Embryogenesis. [Masters Thesis]. Victoria University of Wellington; 2020. Available from: http://hdl.handle.net/10063/8989


University of Southern California

5. Froelich, Steven Michael. Engineering lentiviral vectors for gene delivery.

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

 The development of lentiviral vectors to deliver genes to specific cell types are useful tools because they have the ability to produce stable transduction, maintain… (more)

Subjects/Keywords: lentivirus; DC-SIGN; dendritic cell

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APA (6th Edition):

Froelich, S. M. (2011). Engineering lentiviral vectors for gene delivery. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/459666/rec/2368

Chicago Manual of Style (16th Edition):

Froelich, Steven Michael. “Engineering lentiviral vectors for gene delivery.” 2011. Doctoral Dissertation, University of Southern California. Accessed March 07, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/459666/rec/2368.

MLA Handbook (7th Edition):

Froelich, Steven Michael. “Engineering lentiviral vectors for gene delivery.” 2011. Web. 07 Mar 2021.

Vancouver:

Froelich SM. Engineering lentiviral vectors for gene delivery. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2021 Mar 07]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/459666/rec/2368.

Council of Science Editors:

Froelich SM. Engineering lentiviral vectors for gene delivery. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/459666/rec/2368


University of Tasmania

6. Casey, NP. The Therapeutic potential of lentivector-delivered RNAi.

Degree: 2010, University of Tasmania

 Many forms of leukaemia are caused by chromosomal translocations, which result in specific and characteristic genomic sequences. Where these sequences are unique to the leukaemic… (more)

Subjects/Keywords: lentivirus; vector; RNAi; shRNA; chrosomal-translocation; leukaemia

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APA (6th Edition):

Casey, N. (2010). The Therapeutic potential of lentivector-delivered RNAi. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/10783/1/01_Casey_front.pdf ; https://eprints.utas.edu.au/10783/2/01_Casey_whole.pdf

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):

Casey, NP. “The Therapeutic potential of lentivector-delivered RNAi.” 2010. Thesis, University of Tasmania. Accessed March 07, 2021. https://eprints.utas.edu.au/10783/1/01_Casey_front.pdf ; https://eprints.utas.edu.au/10783/2/01_Casey_whole.pdf.

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

MLA Handbook (7th Edition):

Casey, NP. “The Therapeutic potential of lentivector-delivered RNAi.” 2010. Web. 07 Mar 2021.

Vancouver:

Casey N. The Therapeutic potential of lentivector-delivered RNAi. [Internet] [Thesis]. University of Tasmania; 2010. [cited 2021 Mar 07]. Available from: https://eprints.utas.edu.au/10783/1/01_Casey_front.pdf ; https://eprints.utas.edu.au/10783/2/01_Casey_whole.pdf.

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

Council of Science Editors:

Casey N. The Therapeutic potential of lentivector-delivered RNAi. [Thesis]. University of Tasmania; 2010. Available from: https://eprints.utas.edu.au/10783/1/01_Casey_front.pdf ; https://eprints.utas.edu.au/10783/2/01_Casey_whole.pdf

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


Purdue University

7. Nichols, Jamieson. Temporal Changes in Routine Health Markers and Their Association with Illness and Mortality Rates in Cats Naturally Infected with Feline Immunodeficiency Virus.

Degree: MS, Veterinary Clinical Science, 2015, Purdue University

 Feline immunodeficiency virus is an important lentiviral infection in cats. Infection is life-long and results in immune compromise, increased susceptibility to opportunistic infections and early… (more)

Subjects/Keywords: cats; feline immunodeficiency virus; FIV; lentivirus; retrovirus

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APA (6th Edition):

Nichols, J. (2015). Temporal Changes in Routine Health Markers and Their Association with Illness and Mortality Rates in Cats Naturally Infected with Feline Immunodeficiency Virus. (Thesis). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_theses/1157

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):

Nichols, Jamieson. “Temporal Changes in Routine Health Markers and Their Association with Illness and Mortality Rates in Cats Naturally Infected with Feline Immunodeficiency Virus.” 2015. Thesis, Purdue University. Accessed March 07, 2021. https://docs.lib.purdue.edu/open_access_theses/1157.

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

MLA Handbook (7th Edition):

Nichols, Jamieson. “Temporal Changes in Routine Health Markers and Their Association with Illness and Mortality Rates in Cats Naturally Infected with Feline Immunodeficiency Virus.” 2015. Web. 07 Mar 2021.

Vancouver:

Nichols J. Temporal Changes in Routine Health Markers and Their Association with Illness and Mortality Rates in Cats Naturally Infected with Feline Immunodeficiency Virus. [Internet] [Thesis]. Purdue University; 2015. [cited 2021 Mar 07]. Available from: https://docs.lib.purdue.edu/open_access_theses/1157.

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

Council of Science Editors:

Nichols J. Temporal Changes in Routine Health Markers and Their Association with Illness and Mortality Rates in Cats Naturally Infected with Feline Immunodeficiency Virus. [Thesis]. Purdue University; 2015. Available from: https://docs.lib.purdue.edu/open_access_theses/1157

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


University of Adelaide

8. Padmanabhan, Harshavardini. Development of lentiviral airway gene therapy aerosol delivery techniques for cystic fibrosis.

Degree: 2019, University of Adelaide

 Lentiviral (LV) vectors show promise as a gene therapy vector for cystic fibrosis (CF). The cystic fibrosis airway gene therapy group (CFARG) based in Adelaide,… (more)

Subjects/Keywords: Gene therapy; aerosols; lentivirus; cystic fibrosis

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

APA (6th Edition):

Padmanabhan, H. (2019). Development of lentiviral airway gene therapy aerosol delivery techniques for cystic fibrosis. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/120704

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):

Padmanabhan, Harshavardini. “Development of lentiviral airway gene therapy aerosol delivery techniques for cystic fibrosis.” 2019. Thesis, University of Adelaide. Accessed March 07, 2021. http://hdl.handle.net/2440/120704.

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

MLA Handbook (7th Edition):

Padmanabhan, Harshavardini. “Development of lentiviral airway gene therapy aerosol delivery techniques for cystic fibrosis.” 2019. Web. 07 Mar 2021.

Vancouver:

Padmanabhan H. Development of lentiviral airway gene therapy aerosol delivery techniques for cystic fibrosis. [Internet] [Thesis]. University of Adelaide; 2019. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2440/120704.

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

Council of Science Editors:

Padmanabhan H. Development of lentiviral airway gene therapy aerosol delivery techniques for cystic fibrosis. [Thesis]. University of Adelaide; 2019. Available from: http://hdl.handle.net/2440/120704

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


Colorado State University

9. Baker, Callie M. Development of ovine placental lactogen deficient pregnancies, The.

Degree: MS(M.S.), Biomedical Sciences, 2014, Colorado State University

 Intrauterine growth restriction (IUGR) results in significant fetal and neonatal mortalities and morbidities. Additionally, infants surviving IUGR experience increased incidence of heart disease, diabetes, hypertension… (more)

Subjects/Keywords: ovine; pregnancy; placental lactogen; IUGR; lentivirus; placenta

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APA (6th Edition):

Baker, C. M. (2014). Development of ovine placental lactogen deficient pregnancies, The. (Masters Thesis). Colorado State University. Retrieved from http://hdl.handle.net/10217/88500

Chicago Manual of Style (16th Edition):

Baker, Callie M. “Development of ovine placental lactogen deficient pregnancies, The.” 2014. Masters Thesis, Colorado State University. Accessed March 07, 2021. http://hdl.handle.net/10217/88500.

MLA Handbook (7th Edition):

Baker, Callie M. “Development of ovine placental lactogen deficient pregnancies, The.” 2014. Web. 07 Mar 2021.

Vancouver:

Baker CM. Development of ovine placental lactogen deficient pregnancies, The. [Internet] [Masters thesis]. Colorado State University; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10217/88500.

Council of Science Editors:

Baker CM. Development of ovine placental lactogen deficient pregnancies, The. [Masters Thesis]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/88500


California State University – Sacramento

10. 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 March 07, 2021. 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 Mar 2021.

Vancouver:

Cicchetto AC. Genetically modified multipotent stromal cells for the treatment of osteoarthritis. [Internet] [Masters thesis]. California State University – Sacramento; 2016. [cited 2021 Mar 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


University of Sydney

11. Li, Alisha Jean-King. Overexpression of DGAT1 in 3T3-L1 Cells by Lentiviral Transduction .

Degree: 2015, University of Sydney

 Adipocytes function as the major storage site for triacylglyerol (TAG) and have important roles as active endocrine cells. It is widely assumed that the endocrine… (more)

Subjects/Keywords: 3T3-L1; Adipocyte; Overexpression; DGAT1; Lentivirus; Transduction

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APA (6th Edition):

Li, A. J. (2015). Overexpression of DGAT1 in 3T3-L1 Cells by Lentiviral Transduction . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/14308

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):

Li, Alisha Jean-King. “Overexpression of DGAT1 in 3T3-L1 Cells by Lentiviral Transduction .” 2015. Thesis, University of Sydney. Accessed March 07, 2021. http://hdl.handle.net/2123/14308.

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

MLA Handbook (7th Edition):

Li, Alisha Jean-King. “Overexpression of DGAT1 in 3T3-L1 Cells by Lentiviral Transduction .” 2015. Web. 07 Mar 2021.

Vancouver:

Li AJ. Overexpression of DGAT1 in 3T3-L1 Cells by Lentiviral Transduction . [Internet] [Thesis]. University of Sydney; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2123/14308.

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

Council of Science Editors:

Li AJ. Overexpression of DGAT1 in 3T3-L1 Cells by Lentiviral Transduction . [Thesis]. University of Sydney; 2015. Available from: http://hdl.handle.net/2123/14308

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


University of New South Wales

12. Ledger, Scott. Use of Short-Hairpin RNA to CCR5, and maC46 Entry Inhibitor Gene-Therapies against HIV infection.

Degree: Clinical School - St Vincent's Hospital, 2016, University of New South Wales

 HIV currently infects 35 million people worldwide and antiretroviral treatments are expensive, lifelong, and fail to provide a cure. Gene therapy provides an alternate approach… (more)

Subjects/Keywords: shRNA; HIV; Gene therapy; CCR5; C46; lentivirus

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APA (6th Edition):

Ledger, S. (2016). Use of Short-Hairpin RNA to CCR5, and maC46 Entry Inhibitor Gene-Therapies against HIV infection. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56230 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40347/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Ledger, Scott. “Use of Short-Hairpin RNA to CCR5, and maC46 Entry Inhibitor Gene-Therapies against HIV infection.” 2016. Doctoral Dissertation, University of New South Wales. Accessed March 07, 2021. http://handle.unsw.edu.au/1959.4/56230 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40347/SOURCE02?view=true.

MLA Handbook (7th Edition):

Ledger, Scott. “Use of Short-Hairpin RNA to CCR5, and maC46 Entry Inhibitor Gene-Therapies against HIV infection.” 2016. Web. 07 Mar 2021.

Vancouver:

Ledger S. Use of Short-Hairpin RNA to CCR5, and maC46 Entry Inhibitor Gene-Therapies against HIV infection. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2021 Mar 07]. Available from: http://handle.unsw.edu.au/1959.4/56230 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40347/SOURCE02?view=true.

Council of Science Editors:

Ledger S. Use of Short-Hairpin RNA to CCR5, and maC46 Entry Inhibitor Gene-Therapies against HIV infection. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/56230 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40347/SOURCE02?view=true


Johannes Gutenberg Universität Mainz

13. Zidan, Mohamed. Lentivirus-mediated knockdown of Galectin-10 and Foxp3 in human immune cells.

Degree: 2013, Johannes Gutenberg Universität Mainz

Die Suppression von autoreaktiven T-Zellen ist eine Funktion von CD4+CD25+ regulatorischen T-Zellen (CD4+CD25+ Tregs). CD4+CD25+ Tregs unterdrücken autoaggressive Immunantworten. Galectin-10 und Foxp3 sind wichtige Proteine,… (more)

Subjects/Keywords: Galectin-10, Foxp3, Tregs, Knockdown, Lentivirus; Galectin-10, Foxp3, Tregs, Knockdown, Lentivirus; Life sciences

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APA (6th Edition):

Zidan, M. (2013). Lentivirus-mediated knockdown of Galectin-10 and Foxp3 in human immune cells. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3478/

Chicago Manual of Style (16th Edition):

Zidan, Mohamed. “Lentivirus-mediated knockdown of Galectin-10 and Foxp3 in human immune cells.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed March 07, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2013/3478/.

MLA Handbook (7th Edition):

Zidan, Mohamed. “Lentivirus-mediated knockdown of Galectin-10 and Foxp3 in human immune cells.” 2013. Web. 07 Mar 2021.

Vancouver:

Zidan M. Lentivirus-mediated knockdown of Galectin-10 and Foxp3 in human immune cells. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2021 Mar 07]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3478/.

Council of Science Editors:

Zidan M. Lentivirus-mediated knockdown of Galectin-10 and Foxp3 in human immune cells. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3478/

14. Hasegawa, Marjorie Yumi. Estudo sobre a transmissibilidade do vírus da artrite encefalite caprina através do sêmen e da placenta.

Degree: PhD, Clínica Veterinária, 2014, University of São Paulo

 Artrite Encefalite Caprina é uma enfermidade infecciosa, multissistêmica, causada pelo vírus da Artrite Encefalite Caprina, que pertence dentre os Lentivírus de Pequenos Ruminantes. Sobre o… (more)

Subjects/Keywords: AGID; Caprine lentivirus; cELISA; cELISA; IDGA; Lentivirus caprino; Nested-PCR; Nested-PCR; Transmissão; Transmission

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APA (6th Edition):

Hasegawa, M. Y. (2014). Estudo sobre a transmissibilidade do vírus da artrite encefalite caprina através do sêmen e da placenta. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10136/tde-07012015-081945/ ;

Chicago Manual of Style (16th Edition):

Hasegawa, Marjorie Yumi. “Estudo sobre a transmissibilidade do vírus da artrite encefalite caprina através do sêmen e da placenta.” 2014. Doctoral Dissertation, University of São Paulo. Accessed March 07, 2021. http://www.teses.usp.br/teses/disponiveis/10/10136/tde-07012015-081945/ ;.

MLA Handbook (7th Edition):

Hasegawa, Marjorie Yumi. “Estudo sobre a transmissibilidade do vírus da artrite encefalite caprina através do sêmen e da placenta.” 2014. Web. 07 Mar 2021.

Vancouver:

Hasegawa MY. Estudo sobre a transmissibilidade do vírus da artrite encefalite caprina através do sêmen e da placenta. [Internet] [Doctoral dissertation]. University of São Paulo; 2014. [cited 2021 Mar 07]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10136/tde-07012015-081945/ ;.

Council of Science Editors:

Hasegawa MY. Estudo sobre a transmissibilidade do vírus da artrite encefalite caprina através do sêmen e da placenta. [Doctoral Dissertation]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/10/10136/tde-07012015-081945/ ;

15. Bose, Deepanwita. Tat-independent lentivirus genomes for vaccination and host/pathogen interaction studies : Génomes de lentivirus Tat indépendants pour des études de vaccination et les interactions hôte/pathogène.

Degree: Docteur es, Virologie - Microbiologie - Immunologie, 2017, Université Grenoble Alpes (ComUE)

 Notre laboratoire a développé un prototype de vaccin unique contre le VIH-1 / SIDA. C'est un un lentivecteur ADN non-intégratif qui a été testé dans… (more)

Subjects/Keywords: Lentivirus; Promoteur; Réplication; Vih/vis; Caev; Immunité; Lentivirus; Promoter; Replication; Hiv/siv; Caev; Immunity; 610

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APA (6th Edition):

Bose, D. (2017). Tat-independent lentivirus genomes for vaccination and host/pathogen interaction studies : Génomes de lentivirus Tat indépendants pour des études de vaccination et les interactions hôte/pathogène. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2017GREAV009

Chicago Manual of Style (16th Edition):

Bose, Deepanwita. “Tat-independent lentivirus genomes for vaccination and host/pathogen interaction studies : Génomes de lentivirus Tat indépendants pour des études de vaccination et les interactions hôte/pathogène.” 2017. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed March 07, 2021. http://www.theses.fr/2017GREAV009.

MLA Handbook (7th Edition):

Bose, Deepanwita. “Tat-independent lentivirus genomes for vaccination and host/pathogen interaction studies : Génomes de lentivirus Tat indépendants pour des études de vaccination et les interactions hôte/pathogène.” 2017. Web. 07 Mar 2021.

Vancouver:

Bose D. Tat-independent lentivirus genomes for vaccination and host/pathogen interaction studies : Génomes de lentivirus Tat indépendants pour des études de vaccination et les interactions hôte/pathogène. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2017. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2017GREAV009.

Council of Science Editors:

Bose D. Tat-independent lentivirus genomes for vaccination and host/pathogen interaction studies : Génomes de lentivirus Tat indépendants pour des études de vaccination et les interactions hôte/pathogène. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2017. Available from: http://www.theses.fr/2017GREAV009

16. Ahmid, Simaa. Analyse fonctionnelle de génomes lentiviraux de primates réplicatifs sous le contrôle des promoteurs du lentivirus caprin CAEV : Modèle d'étude pour la latence et persistance des lentivirus : Functional analysis of replication-competent primate lentivirus genomes driven by CAEV promoters : A new model to study latency and persistence.

Degree: Docteur es, Virologie - Microbiologie - Immunologie, 2017, Université Grenoble Alpes (ComUE)

Le syndrome d'immunodéficience acquise (SIDA) est une maladie provoquée chez l'homme par le virus de l'immunodéficience humaine (VIH), un lentivirus à ARN monocaténaire qui infecte… (more)

Subjects/Keywords: Lentivirus; Pathogénèse; Latence; Persistence; Atténuation; Lentivirus; Pathogenesis; Latency; Persistence; Attenuation; 616.91; 579.2

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APA (6th Edition):

Ahmid, S. (2017). Analyse fonctionnelle de génomes lentiviraux de primates réplicatifs sous le contrôle des promoteurs du lentivirus caprin CAEV : Modèle d'étude pour la latence et persistance des lentivirus : Functional analysis of replication-competent primate lentivirus genomes driven by CAEV promoters : A new model to study latency and persistence. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2017GREAV018

Chicago Manual of Style (16th Edition):

Ahmid, Simaa. “Analyse fonctionnelle de génomes lentiviraux de primates réplicatifs sous le contrôle des promoteurs du lentivirus caprin CAEV : Modèle d'étude pour la latence et persistance des lentivirus : Functional analysis of replication-competent primate lentivirus genomes driven by CAEV promoters : A new model to study latency and persistence.” 2017. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed March 07, 2021. http://www.theses.fr/2017GREAV018.

MLA Handbook (7th Edition):

Ahmid, Simaa. “Analyse fonctionnelle de génomes lentiviraux de primates réplicatifs sous le contrôle des promoteurs du lentivirus caprin CAEV : Modèle d'étude pour la latence et persistance des lentivirus : Functional analysis of replication-competent primate lentivirus genomes driven by CAEV promoters : A new model to study latency and persistence.” 2017. Web. 07 Mar 2021.

Vancouver:

Ahmid S. Analyse fonctionnelle de génomes lentiviraux de primates réplicatifs sous le contrôle des promoteurs du lentivirus caprin CAEV : Modèle d'étude pour la latence et persistance des lentivirus : Functional analysis of replication-competent primate lentivirus genomes driven by CAEV promoters : A new model to study latency and persistence. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2017. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2017GREAV018.

Council of Science Editors:

Ahmid S. Analyse fonctionnelle de génomes lentiviraux de primates réplicatifs sous le contrôle des promoteurs du lentivirus caprin CAEV : Modèle d'étude pour la latence et persistance des lentivirus : Functional analysis of replication-competent primate lentivirus genomes driven by CAEV promoters : A new model to study latency and persistence. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2017. Available from: http://www.theses.fr/2017GREAV018

17. Antonia Regina Sessa da Silva. Diagnóstico da Anemia Infecciosa Eqüina: análise comparativa de sistemas comerciais de diagnóstico por imunodifusão.

Degree: 2007, Universidade Federal Rural do Rio de Janeiro

O Brasil possui atualmente o segundo maior rebanho de eqüídeos do mundo e a Eqüideocultura Brasileira desempenha um importante papel no desenvolvimento do setor de… (more)

Subjects/Keywords: anemia infecciosa eqüina; eqüinos; eqüídeos; lentivirus; retrovirus; diagnóstico e IDGA.; MEDICINA VETERINARIA; equine infectious anemia; equines; lentivirus; retrovirus

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APA (6th Edition):

Silva, A. R. S. d. (2007). Diagnóstico da Anemia Infecciosa Eqüina: análise comparativa de sistemas comerciais de diagnóstico por imunodifusão. (Thesis). Universidade Federal Rural do Rio de Janeiro. Retrieved from http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=807

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):

Silva, Antonia Regina Sessa da. “Diagnóstico da Anemia Infecciosa Eqüina: análise comparativa de sistemas comerciais de diagnóstico por imunodifusão.” 2007. Thesis, Universidade Federal Rural do Rio de Janeiro. Accessed March 07, 2021. http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=807.

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

MLA Handbook (7th Edition):

Silva, Antonia Regina Sessa da. “Diagnóstico da Anemia Infecciosa Eqüina: análise comparativa de sistemas comerciais de diagnóstico por imunodifusão.” 2007. Web. 07 Mar 2021.

Vancouver:

Silva ARSd. Diagnóstico da Anemia Infecciosa Eqüina: análise comparativa de sistemas comerciais de diagnóstico por imunodifusão. [Internet] [Thesis]. Universidade Federal Rural do Rio de Janeiro; 2007. [cited 2021 Mar 07]. Available from: http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=807.

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

Council of Science Editors:

Silva ARSd. Diagnóstico da Anemia Infecciosa Eqüina: análise comparativa de sistemas comerciais de diagnóstico por imunodifusão. [Thesis]. Universidade Federal Rural do Rio de Janeiro; 2007. Available from: http://bdtd.ufrrj.br//tde_busca/arquivo.php?codArquivo=807

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

18. Chougui, Ghina. Antagonism of HUSH restriction by lentiviral Vpx and Vpr proteins : Antagonisme de la restriction du complexe HUSH par les protéines lentivirales Vpx et Vpr.

Degree: Docteur es, Microbiologie, 2018, Sorbonne Paris Cité

Les rétrovirus VIH-1 et 2 responsables du SIDA, bien que très similaires sur le plan de leur organisation génomique, diffèrent par leurs protéines auxiliaires. Ces… (more)

Subjects/Keywords: Lentivirus; Vih; Vpr; Vpx; Facteur de restriction; Complexe HUSH; Lentivirus; Hiv; Vpr; Vpx; Restriction factor; HUSH complex; 579.25

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APA (6th Edition):

Chougui, G. (2018). Antagonism of HUSH restriction by lentiviral Vpx and Vpr proteins : Antagonisme de la restriction du complexe HUSH par les protéines lentivirales Vpx et Vpr. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2018USPCB080

Chicago Manual of Style (16th Edition):

Chougui, Ghina. “Antagonism of HUSH restriction by lentiviral Vpx and Vpr proteins : Antagonisme de la restriction du complexe HUSH par les protéines lentivirales Vpx et Vpr.” 2018. Doctoral Dissertation, Sorbonne Paris Cité. Accessed March 07, 2021. http://www.theses.fr/2018USPCB080.

MLA Handbook (7th Edition):

Chougui, Ghina. “Antagonism of HUSH restriction by lentiviral Vpx and Vpr proteins : Antagonisme de la restriction du complexe HUSH par les protéines lentivirales Vpx et Vpr.” 2018. Web. 07 Mar 2021.

Vancouver:

Chougui G. Antagonism of HUSH restriction by lentiviral Vpx and Vpr proteins : Antagonisme de la restriction du complexe HUSH par les protéines lentivirales Vpx et Vpr. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2018. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2018USPCB080.

Council of Science Editors:

Chougui G. Antagonism of HUSH restriction by lentiviral Vpx and Vpr proteins : Antagonisme de la restriction du complexe HUSH par les protéines lentivirales Vpx et Vpr. [Doctoral Dissertation]. Sorbonne Paris Cité; 2018. Available from: http://www.theses.fr/2018USPCB080


NSYSU

19. Chen, Man-Jing. Remote control of lentivirus for RNA interference therapy.

Degree: Master, Institute of Medical Science and Technology, 2016, NSYSU

 Clinical virotherapy has been successfully approved for use in cancer treatment by the US Food and Drug Administration (FDA). Innovative treatment of cancer, oncolytic viruses… (more)

Subjects/Keywords: RNA interference; Short hairpin RNA; Micro-transduction; Lentivirus; Magnetic nanoparticles

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APA (6th Edition):

Chen, M. (2016). Remote control of lentivirus for RNA interference therapy. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725116-122157

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):

Chen, Man-Jing. “Remote control of lentivirus for RNA interference therapy.” 2016. Thesis, NSYSU. Accessed March 07, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725116-122157.

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

MLA Handbook (7th Edition):

Chen, Man-Jing. “Remote control of lentivirus for RNA interference therapy.” 2016. Web. 07 Mar 2021.

Vancouver:

Chen M. Remote control of lentivirus for RNA interference therapy. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Mar 07]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725116-122157.

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

Council of Science Editors:

Chen M. Remote control of lentivirus for RNA interference therapy. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725116-122157

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


California State University – Northridge

20. Kawashima, Ryoko Lala. Regulatory functions of lipoprotein lipase on the cholesterol transporter ATP-binding cassette transporter A1.

Degree: MS, Chemistry and Biochemistry, 2014, California State University – Northridge

 Atherosclerosis is an inflammatory disorder triggered by an accumulation of cholesterol in macrophage-derived foam cells. Adherence of these cells to the vascular endothelium, leads to… (more)

Subjects/Keywords: Lentivirus (siRNA) technology; Dissertations, Academic  – CSUN  – Chemistry and Biochemistry  – Biochemistry.

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APA (6th Edition):

Kawashima, R. L. (2014). Regulatory functions of lipoprotein lipase on the cholesterol transporter ATP-binding cassette transporter A1. (Masters Thesis). California State University – Northridge. Retrieved from http://hdl.handle.net/10211.2/5013

Chicago Manual of Style (16th Edition):

Kawashima, Ryoko Lala. “Regulatory functions of lipoprotein lipase on the cholesterol transporter ATP-binding cassette transporter A1.” 2014. Masters Thesis, California State University – Northridge. Accessed March 07, 2021. http://hdl.handle.net/10211.2/5013.

MLA Handbook (7th Edition):

Kawashima, Ryoko Lala. “Regulatory functions of lipoprotein lipase on the cholesterol transporter ATP-binding cassette transporter A1.” 2014. Web. 07 Mar 2021.

Vancouver:

Kawashima RL. Regulatory functions of lipoprotein lipase on the cholesterol transporter ATP-binding cassette transporter A1. [Internet] [Masters thesis]. California State University – Northridge; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10211.2/5013.

Council of Science Editors:

Kawashima RL. Regulatory functions of lipoprotein lipase on the cholesterol transporter ATP-binding cassette transporter A1. [Masters Thesis]. California State University – Northridge; 2014. Available from: http://hdl.handle.net/10211.2/5013


Penn State University

21. Kazi, Abid A. ROLE OF PRAS40 AND DEPTOR – TWO mTOR BINDING PROTEINS IN C2C12 MYOCYTES .

Degree: 2011, Penn State University

 PRAS40 and DEPTOR are mTOR binding proteins that affect cell metabolism. Under catabolic conditions such as sepsis and glucocorticoid excess, there is an increase in… (more)

Subjects/Keywords: protein synthesis; mTOR; knockdown; lentivirus; shRNA; sepsis; disuse atrophy

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APA (6th Edition):

Kazi, A. A. (2011). ROLE OF PRAS40 AND DEPTOR – TWO mTOR BINDING PROTEINS IN C2C12 MYOCYTES . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11847

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):

Kazi, Abid A. “ROLE OF PRAS40 AND DEPTOR – TWO mTOR BINDING PROTEINS IN C2C12 MYOCYTES .” 2011. Thesis, Penn State University. Accessed March 07, 2021. https://submit-etda.libraries.psu.edu/catalog/11847.

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

MLA Handbook (7th Edition):

Kazi, Abid A. “ROLE OF PRAS40 AND DEPTOR – TWO mTOR BINDING PROTEINS IN C2C12 MYOCYTES .” 2011. Web. 07 Mar 2021.

Vancouver:

Kazi AA. ROLE OF PRAS40 AND DEPTOR – TWO mTOR BINDING PROTEINS IN C2C12 MYOCYTES . [Internet] [Thesis]. Penn State University; 2011. [cited 2021 Mar 07]. Available from: https://submit-etda.libraries.psu.edu/catalog/11847.

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

Council of Science Editors:

Kazi AA. ROLE OF PRAS40 AND DEPTOR – TWO mTOR BINDING PROTEINS IN C2C12 MYOCYTES . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/11847

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

22. Tessanne, Kimberly J. Development of Transgenic Livestock with Reduced Myostatin Expression Using RNA Interference.

Degree: PhD, Veterinary Physiology, 2012, Texas A&M University

 RNA interference (RNAi) is a means of regulating gene expression by targeting mRNA in a sequence-specific manner for degradation or translational inhibition. Short hairpin RNAs… (more)

Subjects/Keywords: transgenic; lentivirus; myostatin

…65 68 74 78 REPLICATION COMPETENT LENTIVIRUS (RCL) ANALYSIS IN RECIPIENT ANIMALS… …injection of lentivirus at the zygote stage .............................. 73 14 Transgenic… …competent lentivirus (RCL).39 Therefore, tests to detect these potential RCL are… …only expressed during in vitro production of recombinant lentivirus.42 Of these same 21… …recombinant lentivirus 17 can be injected into an oocyte or zygote prior to embryo transfer in… 

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APA (6th Edition):

Tessanne, K. J. (2012). Development of Transgenic Livestock with Reduced Myostatin Expression Using RNA Interference. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7594

Chicago Manual of Style (16th Edition):

Tessanne, Kimberly J. “Development of Transgenic Livestock with Reduced Myostatin Expression Using RNA Interference.” 2012. Doctoral Dissertation, Texas A&M University. Accessed March 07, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7594.

MLA Handbook (7th Edition):

Tessanne, Kimberly J. “Development of Transgenic Livestock with Reduced Myostatin Expression Using RNA Interference.” 2012. Web. 07 Mar 2021.

Vancouver:

Tessanne KJ. Development of Transgenic Livestock with Reduced Myostatin Expression Using RNA Interference. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7594.

Council of Science Editors:

Tessanne KJ. Development of Transgenic Livestock with Reduced Myostatin Expression Using RNA Interference. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7594


North Carolina State University

23. Jia, Bin. Role of the Cytoplasmic Tail of Equine Infectious Anemia Virus Transmembrane Glycoprotein in Acute Disease Induction.

Degree: PhD, Comparative Biomedical Sciences, 2004, North Carolina State University

 Equine infectious anemia virus (EIAV) is a macrophage-tropic lentivirus of horses. EIAV is unique among lentiviruses in that a further cleavage event occurs within the… (more)

Subjects/Keywords: EIAV; cytoplasmic tail; lentivirus pathogenesis

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APA (6th Edition):

Jia, B. (2004). Role of the Cytoplasmic Tail of Equine Infectious Anemia Virus Transmembrane Glycoprotein in Acute Disease Induction. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/5331

Chicago Manual of Style (16th Edition):

Jia, Bin. “Role of the Cytoplasmic Tail of Equine Infectious Anemia Virus Transmembrane Glycoprotein in Acute Disease Induction.” 2004. Doctoral Dissertation, North Carolina State University. Accessed March 07, 2021. http://www.lib.ncsu.edu/resolver/1840.16/5331.

MLA Handbook (7th Edition):

Jia, Bin. “Role of the Cytoplasmic Tail of Equine Infectious Anemia Virus Transmembrane Glycoprotein in Acute Disease Induction.” 2004. Web. 07 Mar 2021.

Vancouver:

Jia B. Role of the Cytoplasmic Tail of Equine Infectious Anemia Virus Transmembrane Glycoprotein in Acute Disease Induction. [Internet] [Doctoral dissertation]. North Carolina State University; 2004. [cited 2021 Mar 07]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5331.

Council of Science Editors:

Jia B. Role of the Cytoplasmic Tail of Equine Infectious Anemia Virus Transmembrane Glycoprotein in Acute Disease Induction. [Doctoral Dissertation]. North Carolina State University; 2004. Available from: http://www.lib.ncsu.edu/resolver/1840.16/5331


University of Adelaide

24. Stocker, Alice. Towards gene therapy for cystic fibrosis airway disease: development of single-dose lentiviral gene transfer for lifetime airway expression.

Degree: 2010, University of Adelaide

 Cystic Fibrosis (CF) is the most common, fatal autosomal recessive disorder affecting the Caucasian population with a frequency of 1 in 2500 live births and… (more)

Subjects/Keywords: cystic fibrosis; gene therapy; airway; lungs; respiratory; lentivirus

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APA (6th Edition):

Stocker, A. (2010). Towards gene therapy for cystic fibrosis airway disease: development of single-dose lentiviral gene transfer for lifetime airway expression. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/65308

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):

Stocker, Alice. “Towards gene therapy for cystic fibrosis airway disease: development of single-dose lentiviral gene transfer for lifetime airway expression.” 2010. Thesis, University of Adelaide. Accessed March 07, 2021. http://hdl.handle.net/2440/65308.

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

MLA Handbook (7th Edition):

Stocker, Alice. “Towards gene therapy for cystic fibrosis airway disease: development of single-dose lentiviral gene transfer for lifetime airway expression.” 2010. Web. 07 Mar 2021.

Vancouver:

Stocker A. Towards gene therapy for cystic fibrosis airway disease: development of single-dose lentiviral gene transfer for lifetime airway expression. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2440/65308.

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

Council of Science Editors:

Stocker A. Towards gene therapy for cystic fibrosis airway disease: development of single-dose lentiviral gene transfer for lifetime airway expression. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/65308

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


Boston University

25. Saxena, Debashree. Two functions of lysyl oxidase like-2 : extracellular matrix maturation and cell proliferation.

Degree: 2016, Boston University

 Lysyl oxidase like-2 (LOXL2) was found to be present extracellularly in primary human gingival fibroblast cells. This project has been primarily focused on investigating our… (more)

Subjects/Keywords: Molecular biology; CCN2; LOXL2; rLOXL2; Collagen accumulation; Lentivirus; Proliferation

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APA (6th Edition):

Saxena, D. (2016). Two functions of lysyl oxidase like-2 : extracellular matrix maturation and cell proliferation. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/18730

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):

Saxena, Debashree. “Two functions of lysyl oxidase like-2 : extracellular matrix maturation and cell proliferation.” 2016. Thesis, Boston University. Accessed March 07, 2021. http://hdl.handle.net/2144/18730.

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

MLA Handbook (7th Edition):

Saxena, Debashree. “Two functions of lysyl oxidase like-2 : extracellular matrix maturation and cell proliferation.” 2016. Web. 07 Mar 2021.

Vancouver:

Saxena D. Two functions of lysyl oxidase like-2 : extracellular matrix maturation and cell proliferation. [Internet] [Thesis]. Boston University; 2016. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2144/18730.

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

Council of Science Editors:

Saxena D. Two functions of lysyl oxidase like-2 : extracellular matrix maturation and cell proliferation. [Thesis]. Boston University; 2016. Available from: http://hdl.handle.net/2144/18730

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


Michigan Technological University

26. Salehi, Nasrin. ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT.

Degree: PhD, Department of Chemical Engineering, 2016, Michigan Technological University

  Localizing the drug at the site of action is one of the most important goals of drug delivery systems. This requires developing a vehicle… (more)

Subjects/Keywords: CD47; Antiphagocytosis; Cancer; Targeting; Lentivirus; RGD; Molecular Biology

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APA (6th Edition):

Salehi, N. (2016). ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT. (Doctoral Dissertation). Michigan Technological University. Retrieved from https://digitalcommons.mtu.edu/etdr/245

Chicago Manual of Style (16th Edition):

Salehi, Nasrin. “ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT.” 2016. Doctoral Dissertation, Michigan Technological University. Accessed March 07, 2021. https://digitalcommons.mtu.edu/etdr/245.

MLA Handbook (7th Edition):

Salehi, Nasrin. “ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT.” 2016. Web. 07 Mar 2021.

Vancouver:

Salehi N. ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT. [Internet] [Doctoral dissertation]. Michigan Technological University; 2016. [cited 2021 Mar 07]. Available from: https://digitalcommons.mtu.edu/etdr/245.

Council of Science Editors:

Salehi N. ENGINEERING ANTIPHAGOCYTIC AND TARGETING THERAPEUTIC CARRIERS FOR CANCER TREATMENT. [Doctoral Dissertation]. Michigan Technological University; 2016. Available from: https://digitalcommons.mtu.edu/etdr/245


University of Minnesota

27. LaRue, Rebecca St. Claire. Dynamics of the mammalian APOBEC3 locus and the relationship between mammalian APOBEC3 and Lentiviral Vif proteins.

Degree: Comparative and Molecular Biosciences, 2010, University of Minnesota

 The mammalian immune system must be dynamic in the face of a diverse and ever-changing array of pathogens. Successful pathogens have evolved to overcome host… (more)

Subjects/Keywords: APOBEC3; Comparative; HIV; Immunity; Lentivirus

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APA (6th Edition):

LaRue, R. S. C. (2010). Dynamics of the mammalian APOBEC3 locus and the relationship between mammalian APOBEC3 and Lentiviral Vif proteins. (Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/97083

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):

LaRue, Rebecca St Claire. “Dynamics of the mammalian APOBEC3 locus and the relationship between mammalian APOBEC3 and Lentiviral Vif proteins.” 2010. Thesis, University of Minnesota. Accessed March 07, 2021. http://purl.umn.edu/97083.

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

MLA Handbook (7th Edition):

LaRue, Rebecca St Claire. “Dynamics of the mammalian APOBEC3 locus and the relationship between mammalian APOBEC3 and Lentiviral Vif proteins.” 2010. Web. 07 Mar 2021.

Vancouver:

LaRue RSC. Dynamics of the mammalian APOBEC3 locus and the relationship between mammalian APOBEC3 and Lentiviral Vif proteins. [Internet] [Thesis]. University of Minnesota; 2010. [cited 2021 Mar 07]. Available from: http://purl.umn.edu/97083.

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

Council of Science Editors:

LaRue RSC. Dynamics of the mammalian APOBEC3 locus and the relationship between mammalian APOBEC3 and Lentiviral Vif proteins. [Thesis]. University of Minnesota; 2010. Available from: http://purl.umn.edu/97083

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


University of Southern California

28. Harboe-Schmidt, Jens Erik. Gene delivery to pulmonary mucosa.

Degree: PhD, Biochemistry & Molecular Biology, 2006, University of Southern California

 We investigated the use of a replication-defective human immunodeficiency virus-based lentivirus vector pseudotyped with VSV.G for GFP gene transfer to primary rat alveolar epithelial cells… (more)

Subjects/Keywords: gene; delivery; lentivirus; pulmonary; mucosa

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

APA (6th Edition):

Harboe-Schmidt, J. E. (2006). Gene delivery to pulmonary mucosa. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/21842/rec/2979

Chicago Manual of Style (16th Edition):

Harboe-Schmidt, Jens Erik. “Gene delivery to pulmonary mucosa.” 2006. Doctoral Dissertation, University of Southern California. Accessed March 07, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/21842/rec/2979.

MLA Handbook (7th Edition):

Harboe-Schmidt, Jens Erik. “Gene delivery to pulmonary mucosa.” 2006. Web. 07 Mar 2021.

Vancouver:

Harboe-Schmidt JE. Gene delivery to pulmonary mucosa. [Internet] [Doctoral dissertation]. University of Southern California; 2006. [cited 2021 Mar 07]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/21842/rec/2979.

Council of Science Editors:

Harboe-Schmidt JE. Gene delivery to pulmonary mucosa. [Doctoral Dissertation]. University of Southern California; 2006. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/21842/rec/2979


University of Kentucky

29. Trimby, Christopher Matthew. STRATEGIES FOR TARGETING LENTIVIRAL VECTORS.

Degree: 2011, University of Kentucky

 Lentiviral gene therapy has held great promise for treating a wide range of neurological disorders due to its ability to stably integrate into the genome… (more)

Subjects/Keywords: Gene Therapy; Neuroscience; Lentivirus; Chimeric Pseudotyping; Vector production; Medical Physiology

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

APA (6th Edition):

Trimby, C. M. (2011). STRATEGIES FOR TARGETING LENTIVIRAL VECTORS. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/gradschool_diss/157

Chicago Manual of Style (16th Edition):

Trimby, Christopher Matthew. “STRATEGIES FOR TARGETING LENTIVIRAL VECTORS.” 2011. Doctoral Dissertation, University of Kentucky. Accessed March 07, 2021. https://uknowledge.uky.edu/gradschool_diss/157.

MLA Handbook (7th Edition):

Trimby, Christopher Matthew. “STRATEGIES FOR TARGETING LENTIVIRAL VECTORS.” 2011. Web. 07 Mar 2021.

Vancouver:

Trimby CM. STRATEGIES FOR TARGETING LENTIVIRAL VECTORS. [Internet] [Doctoral dissertation]. University of Kentucky; 2011. [cited 2021 Mar 07]. Available from: https://uknowledge.uky.edu/gradschool_diss/157.

Council of Science Editors:

Trimby CM. STRATEGIES FOR TARGETING LENTIVIRAL VECTORS. [Doctoral Dissertation]. University of Kentucky; 2011. Available from: https://uknowledge.uky.edu/gradschool_diss/157

30. Harrington, Lauriane. The role of β4-containing nicotinic acetylcholine receptors in nicotine addiction : Rôle des récepteurs nicotiniques de l’acétylcholine contenant la sous-unité β4 dans l’addiction à la nicotine.

Degree: Docteur es, Neurosciences, 2015, Université Pierre et Marie Curie – Paris VI

Le tabac est consommé par environ un milliard de personnes. D'après l'Organisation Mondiale de la Santé, le tabagisme est la première cause évitable de mortalité… (more)

Subjects/Keywords: Nicotine; Récompense; Aversif; Lentivirus; Récepteurs; Acétylcholine; Nicotine; Receptors; 616.865

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

APA (6th Edition):

Harrington, L. (2015). The role of β4-containing nicotinic acetylcholine receptors in nicotine addiction : Rôle des récepteurs nicotiniques de l’acétylcholine contenant la sous-unité β4 dans l’addiction à la nicotine. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2015PA066328

Chicago Manual of Style (16th Edition):

Harrington, Lauriane. “The role of β4-containing nicotinic acetylcholine receptors in nicotine addiction : Rôle des récepteurs nicotiniques de l’acétylcholine contenant la sous-unité β4 dans l’addiction à la nicotine.” 2015. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed March 07, 2021. http://www.theses.fr/2015PA066328.

MLA Handbook (7th Edition):

Harrington, Lauriane. “The role of β4-containing nicotinic acetylcholine receptors in nicotine addiction : Rôle des récepteurs nicotiniques de l’acétylcholine contenant la sous-unité β4 dans l’addiction à la nicotine.” 2015. Web. 07 Mar 2021.

Vancouver:

Harrington L. The role of β4-containing nicotinic acetylcholine receptors in nicotine addiction : Rôle des récepteurs nicotiniques de l’acétylcholine contenant la sous-unité β4 dans l’addiction à la nicotine. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. [cited 2021 Mar 07]. Available from: http://www.theses.fr/2015PA066328.

Council of Science Editors:

Harrington L. The role of β4-containing nicotinic acetylcholine receptors in nicotine addiction : Rôle des récepteurs nicotiniques de l’acétylcholine contenant la sous-unité β4 dans l’addiction à la nicotine. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. Available from: http://www.theses.fr/2015PA066328

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