Advanced search options

Advanced Search Options 🞨

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

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(genome editing). Showing records 1 – 30 of 129 total matches.

[1] [2] [3] [4] [5]

Search Limiters

Last 2 Years | English Only

Degrees

Country

▼ Search Limiters


Harvard University

1. Rees, Holly A. Expanding the Capabilities of Genome Editing.

Degree: PhD, 2019, Harvard University

 The ability to precisely and efficiently edit DNA sequences within the genome of living cells has been a major goal of the life sciences since… (more)

Subjects/Keywords: Base editing; genome editing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rees, H. A. (2019). Expanding the Capabilities of Genome Editing. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029513

Chicago Manual of Style (16th Edition):

Rees, Holly A. “Expanding the Capabilities of Genome Editing.” 2019. Doctoral Dissertation, Harvard University. Accessed January 20, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029513.

MLA Handbook (7th Edition):

Rees, Holly A. “Expanding the Capabilities of Genome Editing.” 2019. Web. 20 Jan 2021.

Vancouver:

Rees HA. Expanding the Capabilities of Genome Editing. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2021 Jan 20]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029513.

Council of Science Editors:

Rees HA. Expanding the Capabilities of Genome Editing. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029513


Georgia Tech

2. Lin, Yanni. Design and optimization of engineered nucleases for genome editing applications.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2014, Georgia Tech

Genome editing mediated by engineered nucleases, including Transcription Activator-Like Effector Nucleases (TALENs) and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) / CRISPR-associated (Cas) systems, holds… (more)

Subjects/Keywords: Genome engineering; Genome editing; TALENs; CRISPRs

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lin, Y. (2014). Design and optimization of engineered nucleases for genome editing applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54249

Chicago Manual of Style (16th Edition):

Lin, Yanni. “Design and optimization of engineered nucleases for genome editing applications.” 2014. Doctoral Dissertation, Georgia Tech. Accessed January 20, 2021. http://hdl.handle.net/1853/54249.

MLA Handbook (7th Edition):

Lin, Yanni. “Design and optimization of engineered nucleases for genome editing applications.” 2014. Web. 20 Jan 2021.

Vancouver:

Lin Y. Design and optimization of engineered nucleases for genome editing applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1853/54249.

Council of Science Editors:

Lin Y. Design and optimization of engineered nucleases for genome editing applications. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54249

3. Wang, Yuemeng. Development of versatile genetic tools to study a DYRK family kinase in Caenorhabditis elegans.

Degree: 2015, Johns Hopkins University

 Screening for suppressors is a common genetic technique to identify mutations in genes that interact with one another. In Caenorhabditis elegans, suppressor screens are commonly… (more)

Subjects/Keywords: Suppressor screen; WGS mapping; Genome editing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, Y. (2015). Development of versatile genetic tools to study a DYRK family kinase in Caenorhabditis elegans. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37917

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, Yuemeng. “Development of versatile genetic tools to study a DYRK family kinase in Caenorhabditis elegans.” 2015. Thesis, Johns Hopkins University. Accessed January 20, 2021. http://jhir.library.jhu.edu/handle/1774.2/37917.

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

MLA Handbook (7th Edition):

Wang, Yuemeng. “Development of versatile genetic tools to study a DYRK family kinase in Caenorhabditis elegans.” 2015. Web. 20 Jan 2021.

Vancouver:

Wang Y. Development of versatile genetic tools to study a DYRK family kinase in Caenorhabditis elegans. [Internet] [Thesis]. Johns Hopkins University; 2015. [cited 2021 Jan 20]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37917.

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

Council of Science Editors:

Wang Y. Development of versatile genetic tools to study a DYRK family kinase in Caenorhabditis elegans. [Thesis]. Johns Hopkins University; 2015. Available from: http://jhir.library.jhu.edu/handle/1774.2/37917

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


University of Saskatchewan

4. Vasquez Arreaga, Oswaldo. CANADIAN CONSUMER PERCEPTION OF GENOME-EDITED FOOD PRODUCTS.

Degree: 2020, University of Saskatchewan

 New Breeding techniques (NBTs) have been developed in the last decade and allow for faster, more precise and less expensive genetic modification of new plant… (more)

Subjects/Keywords: New breeding techniques; genome editing; consumer perception

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vasquez Arreaga, O. (2020). CANADIAN CONSUMER PERCEPTION OF GENOME-EDITED FOOD PRODUCTS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12841

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):

Vasquez Arreaga, Oswaldo. “CANADIAN CONSUMER PERCEPTION OF GENOME-EDITED FOOD PRODUCTS.” 2020. Thesis, University of Saskatchewan. Accessed January 20, 2021. http://hdl.handle.net/10388/12841.

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

MLA Handbook (7th Edition):

Vasquez Arreaga, Oswaldo. “CANADIAN CONSUMER PERCEPTION OF GENOME-EDITED FOOD PRODUCTS.” 2020. Web. 20 Jan 2021.

Vancouver:

Vasquez Arreaga O. CANADIAN CONSUMER PERCEPTION OF GENOME-EDITED FOOD PRODUCTS. [Internet] [Thesis]. University of Saskatchewan; 2020. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10388/12841.

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

Council of Science Editors:

Vasquez Arreaga O. CANADIAN CONSUMER PERCEPTION OF GENOME-EDITED FOOD PRODUCTS. [Thesis]. University of Saskatchewan; 2020. Available from: http://hdl.handle.net/10388/12841

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


Texas A&M University

5. Pinzon Arteaga, Carlos Andres. PRECISE AND EFFICIENT THERAPEUTIC GENOME EDITING FOR THE CORRECTION OF GENETIC DISEASES IN ANIMALS.

Degree: MS, Biomedical Sciences, 2017, Texas A&M University

 There are more than 6,052 identified genetic mutations linked to disease in humans and animals. Thanks to the advent of gene editing based on programmable… (more)

Subjects/Keywords: genome editing; CRISPR; genetic engineering; CRISPR-Cas9

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pinzon Arteaga, C. A. (2017). PRECISE AND EFFICIENT THERAPEUTIC GENOME EDITING FOR THE CORRECTION OF GENETIC DISEASES IN ANIMALS. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187291

Chicago Manual of Style (16th Edition):

Pinzon Arteaga, Carlos Andres. “PRECISE AND EFFICIENT THERAPEUTIC GENOME EDITING FOR THE CORRECTION OF GENETIC DISEASES IN ANIMALS.” 2017. Masters Thesis, Texas A&M University. Accessed January 20, 2021. http://hdl.handle.net/1969.1/187291.

MLA Handbook (7th Edition):

Pinzon Arteaga, Carlos Andres. “PRECISE AND EFFICIENT THERAPEUTIC GENOME EDITING FOR THE CORRECTION OF GENETIC DISEASES IN ANIMALS.” 2017. Web. 20 Jan 2021.

Vancouver:

Pinzon Arteaga CA. PRECISE AND EFFICIENT THERAPEUTIC GENOME EDITING FOR THE CORRECTION OF GENETIC DISEASES IN ANIMALS. [Internet] [Masters thesis]. Texas A&M University; 2017. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1969.1/187291.

Council of Science Editors:

Pinzon Arteaga CA. PRECISE AND EFFICIENT THERAPEUTIC GENOME EDITING FOR THE CORRECTION OF GENETIC DISEASES IN ANIMALS. [Masters Thesis]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/187291


Harvard University

6. Lin, ChieYu. Characterization and Optimization of the CRISPR/Cas System for Applications in Genome Engineering.

Degree: Doctor of Medicine, 2014, Harvard University

 The ability to precisely manipulate the genome in a targeted manner is fundamental to driving both basic science research and development of medical therapeutics. Until… (more)

Subjects/Keywords: Genome editing; CRISPR-Cas; Molecular Biology; Cas9

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lin, C. (2014). Characterization and Optimization of the CRISPR/Cas System for Applications in Genome Engineering. (Doctoral Dissertation). Harvard University. Retrieved from http://etds.lib.harvard.edu/hms/admin/view/61 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407619

Chicago Manual of Style (16th Edition):

Lin, ChieYu. “Characterization and Optimization of the CRISPR/Cas System for Applications in Genome Engineering.” 2014. Doctoral Dissertation, Harvard University. Accessed January 20, 2021. http://etds.lib.harvard.edu/hms/admin/view/61 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407619.

MLA Handbook (7th Edition):

Lin, ChieYu. “Characterization and Optimization of the CRISPR/Cas System for Applications in Genome Engineering.” 2014. Web. 20 Jan 2021.

Vancouver:

Lin C. Characterization and Optimization of the CRISPR/Cas System for Applications in Genome Engineering. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2021 Jan 20]. Available from: http://etds.lib.harvard.edu/hms/admin/view/61 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407619.

Council of Science Editors:

Lin C. Characterization and Optimization of the CRISPR/Cas System for Applications in Genome Engineering. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://etds.lib.harvard.edu/hms/admin/view/61 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407619


York University

7. Ma, Myat Su Nwe. Tagging Endogenous H2A.Z1 and H2A.Z2 Histone Variant Isoforms Using CRISPR-Cas9 and Identifying SUMOylated Proteins in Proximity to H2A.Z-Containing Nucleosomes.

Degree: MSc -MS, Biology, 2018, York University

 H2A.Z is a variant of the H2A core histone, and is well known to be important for transcriptional regulation in eukaryotic cells. It was recently… (more)

Subjects/Keywords: Biology; CRISPR-Cas9; Genome Editing; Epigenetics; Histones

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ma, M. S. N. (2018). Tagging Endogenous H2A.Z1 and H2A.Z2 Histone Variant Isoforms Using CRISPR-Cas9 and Identifying SUMOylated Proteins in Proximity to H2A.Z-Containing Nucleosomes. (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/35593

Chicago Manual of Style (16th Edition):

Ma, Myat Su Nwe. “Tagging Endogenous H2A.Z1 and H2A.Z2 Histone Variant Isoforms Using CRISPR-Cas9 and Identifying SUMOylated Proteins in Proximity to H2A.Z-Containing Nucleosomes.” 2018. Masters Thesis, York University. Accessed January 20, 2021. http://hdl.handle.net/10315/35593.

MLA Handbook (7th Edition):

Ma, Myat Su Nwe. “Tagging Endogenous H2A.Z1 and H2A.Z2 Histone Variant Isoforms Using CRISPR-Cas9 and Identifying SUMOylated Proteins in Proximity to H2A.Z-Containing Nucleosomes.” 2018. Web. 20 Jan 2021.

Vancouver:

Ma MSN. Tagging Endogenous H2A.Z1 and H2A.Z2 Histone Variant Isoforms Using CRISPR-Cas9 and Identifying SUMOylated Proteins in Proximity to H2A.Z-Containing Nucleosomes. [Internet] [Masters thesis]. York University; 2018. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10315/35593.

Council of Science Editors:

Ma MSN. Tagging Endogenous H2A.Z1 and H2A.Z2 Histone Variant Isoforms Using CRISPR-Cas9 and Identifying SUMOylated Proteins in Proximity to H2A.Z-Containing Nucleosomes. [Masters Thesis]. York University; 2018. Available from: http://hdl.handle.net/10315/35593


Rice University

8. Pan, Yidan. Profiling Genome Editing Outcomes for Biological Studies and Disease Treatment.

Degree: PhD, Natural Sciences, 2020, Rice University

 CRISPR/Cas9 systems are designed to make site- and sequence-specific alterations to the genomes of a wide variety of organisms by targeting with user-defined guide RNAs… (more)

Subjects/Keywords: CRISPR/Cas9; genome editing; eQTL; mutagenesis profiling

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pan, Y. (2020). Profiling Genome Editing Outcomes for Biological Studies and Disease Treatment. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/108440

Chicago Manual of Style (16th Edition):

Pan, Yidan. “Profiling Genome Editing Outcomes for Biological Studies and Disease Treatment.” 2020. Doctoral Dissertation, Rice University. Accessed January 20, 2021. http://hdl.handle.net/1911/108440.

MLA Handbook (7th Edition):

Pan, Yidan. “Profiling Genome Editing Outcomes for Biological Studies and Disease Treatment.” 2020. Web. 20 Jan 2021.

Vancouver:

Pan Y. Profiling Genome Editing Outcomes for Biological Studies and Disease Treatment. [Internet] [Doctoral dissertation]. Rice University; 2020. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1911/108440.

Council of Science Editors:

Pan Y. Profiling Genome Editing Outcomes for Biological Studies and Disease Treatment. [Doctoral Dissertation]. Rice University; 2020. Available from: http://hdl.handle.net/1911/108440


University of Minnesota

9. Wheelwright, Matthew. Human iPSC-Derived Cardiac Myocytes: Toward an In Vitro Model of Cardiac Physiology.

Degree: PhD, Integrative Biology and Physiology, 2017, University of Minnesota

 Cardiovascular Disease is a growing public health issue in the modern world, with a high incidence rate that continues to increase, and poor mortality rates.… (more)

Subjects/Keywords: Cardiomyocyte; Development; Force; Genome Editing; Stem Cell

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wheelwright, M. (2017). Human iPSC-Derived Cardiac Myocytes: Toward an In Vitro Model of Cardiac Physiology. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/188928

Chicago Manual of Style (16th Edition):

Wheelwright, Matthew. “Human iPSC-Derived Cardiac Myocytes: Toward an In Vitro Model of Cardiac Physiology.” 2017. Doctoral Dissertation, University of Minnesota. Accessed January 20, 2021. http://hdl.handle.net/11299/188928.

MLA Handbook (7th Edition):

Wheelwright, Matthew. “Human iPSC-Derived Cardiac Myocytes: Toward an In Vitro Model of Cardiac Physiology.” 2017. Web. 20 Jan 2021.

Vancouver:

Wheelwright M. Human iPSC-Derived Cardiac Myocytes: Toward an In Vitro Model of Cardiac Physiology. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/11299/188928.

Council of Science Editors:

Wheelwright M. Human iPSC-Derived Cardiac Myocytes: Toward an In Vitro Model of Cardiac Physiology. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/188928


University of Minnesota

10. St. Martin, Amber. Improved Base Editing Technologies With Novel Editors and Assays.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2018, University of Minnesota

Genome engineering is a rapidly evolving area of study. One driver of the breakneck speed with which the field is moving forward is the application… (more)

Subjects/Keywords: APOBEC; Base Editing; Cas9; CRISPR; Engineering; Genome

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

St. Martin, A. (2018). Improved Base Editing Technologies With Novel Editors and Assays. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/201721

Chicago Manual of Style (16th Edition):

St. Martin, Amber. “Improved Base Editing Technologies With Novel Editors and Assays.” 2018. Doctoral Dissertation, University of Minnesota. Accessed January 20, 2021. http://hdl.handle.net/11299/201721.

MLA Handbook (7th Edition):

St. Martin, Amber. “Improved Base Editing Technologies With Novel Editors and Assays.” 2018. Web. 20 Jan 2021.

Vancouver:

St. Martin A. Improved Base Editing Technologies With Novel Editors and Assays. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/11299/201721.

Council of Science Editors:

St. Martin A. Improved Base Editing Technologies With Novel Editors and Assays. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/201721


University of Minnesota

11. Domenech Corts, Anna. Efficient and Precise Genome Editing in Shewanella with Recombineering and CRISPR/Cas9-mediated Counter-selection.

Degree: PhD, Plant and Microbial Biology, 2019, University of Minnesota

 Shewanella are invaluable hosts for the discovery and engineering of pathways important for bioremediation of toxic and radioactive metals, to create microbial fuel cells and… (more)

Subjects/Keywords: CRISPR/Cas9; genome editing; recombineering; Shewanella

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Domenech Corts, A. (2019). Efficient and Precise Genome Editing in Shewanella with Recombineering and CRISPR/Cas9-mediated Counter-selection. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/206302

Chicago Manual of Style (16th Edition):

Domenech Corts, Anna. “Efficient and Precise Genome Editing in Shewanella with Recombineering and CRISPR/Cas9-mediated Counter-selection.” 2019. Doctoral Dissertation, University of Minnesota. Accessed January 20, 2021. http://hdl.handle.net/11299/206302.

MLA Handbook (7th Edition):

Domenech Corts, Anna. “Efficient and Precise Genome Editing in Shewanella with Recombineering and CRISPR/Cas9-mediated Counter-selection.” 2019. Web. 20 Jan 2021.

Vancouver:

Domenech Corts A. Efficient and Precise Genome Editing in Shewanella with Recombineering and CRISPR/Cas9-mediated Counter-selection. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/11299/206302.

Council of Science Editors:

Domenech Corts A. Efficient and Precise Genome Editing in Shewanella with Recombineering and CRISPR/Cas9-mediated Counter-selection. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/206302

12. Li, Ting. Function and application of TAL effectors.

Degree: 2014, Iowa State University

 The transcription activator-like effectors (TALE) are the largest family of the type III effector proteins from Xanthomonas spp. Each TALE contains an N-terminal signal for… (more)

Subjects/Keywords: genome editing; genome modification; TAL effector; TAL effector nuclease; Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, T. (2014). Function and application of TAL effectors. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/13875

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, Ting. “Function and application of TAL effectors.” 2014. Thesis, Iowa State University. Accessed January 20, 2021. https://lib.dr.iastate.edu/etd/13875.

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

MLA Handbook (7th Edition):

Li, Ting. “Function and application of TAL effectors.” 2014. Web. 20 Jan 2021.

Vancouver:

Li T. Function and application of TAL effectors. [Internet] [Thesis]. Iowa State University; 2014. [cited 2021 Jan 20]. Available from: https://lib.dr.iastate.edu/etd/13875.

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

Council of Science Editors:

Li T. Function and application of TAL effectors. [Thesis]. Iowa State University; 2014. Available from: https://lib.dr.iastate.edu/etd/13875

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


University of Pennsylvania

13. Sharma, Rajiv. In Vivo Genome Editing: Proof of Concept in Neonatal and Adult Mouse Liver.

Degree: 2015, University of Pennsylvania

 Adeno-associated viral (AAV) vectors show great potential for therapeutic gene delivery for monogenic diseases, including hemophilia. Major limitations of this approach are the inability to… (more)

Subjects/Keywords: Gene Therapy; Genome Editing; Genome Engineering; Hemophilia; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sharma, R. (2015). In Vivo Genome Editing: Proof of Concept in Neonatal and Adult Mouse Liver. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1130

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):

Sharma, Rajiv. “In Vivo Genome Editing: Proof of Concept in Neonatal and Adult Mouse Liver.” 2015. Thesis, University of Pennsylvania. Accessed January 20, 2021. https://repository.upenn.edu/edissertations/1130.

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

MLA Handbook (7th Edition):

Sharma, Rajiv. “In Vivo Genome Editing: Proof of Concept in Neonatal and Adult Mouse Liver.” 2015. Web. 20 Jan 2021.

Vancouver:

Sharma R. In Vivo Genome Editing: Proof of Concept in Neonatal and Adult Mouse Liver. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2021 Jan 20]. Available from: https://repository.upenn.edu/edissertations/1130.

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

Council of Science Editors:

Sharma R. In Vivo Genome Editing: Proof of Concept in Neonatal and Adult Mouse Liver. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1130

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


Georgia Tech

14. Fine, Eli Jacob. A toolkit for analysis of gene editing and off-target effects of engineered nucleases.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2015, Georgia Tech

 Several tools were developed to help researchers facilitate clinical translation of the use of engineered nucleases towards their disease gene of interest. Two major issues… (more)

Subjects/Keywords: Genome editing; Genome engineering; Engineered nucleases; Off-target effects; TALENs; ZFNs; CRISPR; Cas9; Gene therapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fine, E. J. (2015). A toolkit for analysis of gene editing and off-target effects of engineered nucleases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54875

Chicago Manual of Style (16th Edition):

Fine, Eli Jacob. “A toolkit for analysis of gene editing and off-target effects of engineered nucleases.” 2015. Doctoral Dissertation, Georgia Tech. Accessed January 20, 2021. http://hdl.handle.net/1853/54875.

MLA Handbook (7th Edition):

Fine, Eli Jacob. “A toolkit for analysis of gene editing and off-target effects of engineered nucleases.” 2015. Web. 20 Jan 2021.

Vancouver:

Fine EJ. A toolkit for analysis of gene editing and off-target effects of engineered nucleases. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1853/54875.

Council of Science Editors:

Fine EJ. A toolkit for analysis of gene editing and off-target effects of engineered nucleases. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54875


Cornell University

15. Dolan, Adam Emin. CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2018, Cornell University

Genome editing techniques and platforms for nucleic acid targeting have been revolutionized by the discovery and technological adaptation of bacterial immune systems called CRISPR systems.… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Cas3; Cascade; CRISPR; Genome Editing; Bioengineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dolan, A. E. (2018). CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/64835

Chicago Manual of Style (16th Edition):

Dolan, Adam Emin. “CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING.” 2018. Doctoral Dissertation, Cornell University. Accessed January 20, 2021. http://hdl.handle.net/1813/64835.

MLA Handbook (7th Edition):

Dolan, Adam Emin. “CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING.” 2018. Web. 20 Jan 2021.

Vancouver:

Dolan AE. CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1813/64835.

Council of Science Editors:

Dolan AE. CHARACTERIZATION OF THE TYPE I-E CRISPR SYSTEM OF T. FUSCA AND ITS APPLICATION TO GENOME EDITING. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/64835


Texas A&M University

16. Morales, Karina Yazmine. CHARACTERIZATION AND VALIDATION OF FLOWERING TIME GENES IN A DIVERSITY PANEL OF RICE (Oryza sativa L.).

Degree: MS, Plant Breeding, 2018, Texas A&M University

 In order to meet the needs of a growing population, rice production must be doubled by 2050 in comparison to 2005 production levels. However, rice… (more)

Subjects/Keywords: Rice; genetics; days to flowering; GWAS; genome editing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Morales, K. Y. (2018). CHARACTERIZATION AND VALIDATION OF FLOWERING TIME GENES IN A DIVERSITY PANEL OF RICE (Oryza sativa L.). (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174070

Chicago Manual of Style (16th Edition):

Morales, Karina Yazmine. “CHARACTERIZATION AND VALIDATION OF FLOWERING TIME GENES IN A DIVERSITY PANEL OF RICE (Oryza sativa L.).” 2018. Masters Thesis, Texas A&M University. Accessed January 20, 2021. http://hdl.handle.net/1969.1/174070.

MLA Handbook (7th Edition):

Morales, Karina Yazmine. “CHARACTERIZATION AND VALIDATION OF FLOWERING TIME GENES IN A DIVERSITY PANEL OF RICE (Oryza sativa L.).” 2018. Web. 20 Jan 2021.

Vancouver:

Morales KY. CHARACTERIZATION AND VALIDATION OF FLOWERING TIME GENES IN A DIVERSITY PANEL OF RICE (Oryza sativa L.). [Internet] [Masters thesis]. Texas A&M University; 2018. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1969.1/174070.

Council of Science Editors:

Morales KY. CHARACTERIZATION AND VALIDATION OF FLOWERING TIME GENES IN A DIVERSITY PANEL OF RICE (Oryza sativa L.). [Masters Thesis]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/174070


Virginia Commonwealth University

17. Robinson, Jason M. Functional Significance of mtDNA Cytosine Modification Tested by Genome Editing.

Degree: MS, Molecular Biology and Genetics, 2016, Virginia Commonwealth University

  The field of epigenetics is gaining popularity and speed, due in part to its capability to answer lingering questions about the root cause of… (more)

Subjects/Keywords: DNMT1; DNMT3B; mitochondria; genome; editing; methyltransferase; Genetics; Integrative Biology; Molecular Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Robinson, J. M. (2016). Functional Significance of mtDNA Cytosine Modification Tested by Genome Editing. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/A612-YW17 ; https://scholarscompass.vcu.edu/etd/4561

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):

Robinson, Jason M. “Functional Significance of mtDNA Cytosine Modification Tested by Genome Editing.” 2016. Thesis, Virginia Commonwealth University. Accessed January 20, 2021. https://doi.org/10.25772/A612-YW17 ; https://scholarscompass.vcu.edu/etd/4561.

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

MLA Handbook (7th Edition):

Robinson, Jason M. “Functional Significance of mtDNA Cytosine Modification Tested by Genome Editing.” 2016. Web. 20 Jan 2021.

Vancouver:

Robinson JM. Functional Significance of mtDNA Cytosine Modification Tested by Genome Editing. [Internet] [Thesis]. Virginia Commonwealth University; 2016. [cited 2021 Jan 20]. Available from: https://doi.org/10.25772/A612-YW17 ; https://scholarscompass.vcu.edu/etd/4561.

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

Council of Science Editors:

Robinson JM. Functional Significance of mtDNA Cytosine Modification Tested by Genome Editing. [Thesis]. Virginia Commonwealth University; 2016. Available from: https://doi.org/10.25772/A612-YW17 ; https://scholarscompass.vcu.edu/etd/4561

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


University of Adelaide

18. Cui, Lun. DNA looping mediated transcriptional regulation.

Degree: 2014, University of Adelaide

 Protein binding to DNA sequences is the foundation of transcriptional regulation. By binding at specific DNA sequences, such as promoters, proteins can recruit other proteins… (more)

Subjects/Keywords: gene regulation; DNA looping; synthetic biology; genome editing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Cui, L. (2014). DNA looping mediated transcriptional regulation. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/92805

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):

Cui, Lun. “DNA looping mediated transcriptional regulation.” 2014. Thesis, University of Adelaide. Accessed January 20, 2021. http://hdl.handle.net/2440/92805.

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

MLA Handbook (7th Edition):

Cui, Lun. “DNA looping mediated transcriptional regulation.” 2014. Web. 20 Jan 2021.

Vancouver:

Cui L. DNA looping mediated transcriptional regulation. [Internet] [Thesis]. University of Adelaide; 2014. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/2440/92805.

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

Council of Science Editors:

Cui L. DNA looping mediated transcriptional regulation. [Thesis]. University of Adelaide; 2014. Available from: http://hdl.handle.net/2440/92805

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

19. Layer, Jacob. POLD2 Promotes Chromosomal Rearrangements and Inaccurate End-Joining in Human Cells.

Degree: PhD, 2019, Harvard University

Chromosomal translocations are recurrent genetic rearrangements with the potential to initiate carcinogenesis. While, the clinical etiology of chromosomal translocations is well established, the mechanisms responsible… (more)

Subjects/Keywords: DSB repair; Genome Editing

…aphidicolin, it being essential for in vitro SV40 genome replication, and that specific inhibition… …genome in mouse embryonic stem cells (mESCs) (Figure 2.1A) (Richardson… …genome of human lung adenocarcinoma A549 cells. These cells are infected with a ZFN expressing… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Layer, J. (2019). POLD2 Promotes Chromosomal Rearrangements and Inaccurate End-Joining in Human Cells. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41121277

Chicago Manual of Style (16th Edition):

Layer, Jacob. “POLD2 Promotes Chromosomal Rearrangements and Inaccurate End-Joining in Human Cells.” 2019. Doctoral Dissertation, Harvard University. Accessed January 20, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41121277.

MLA Handbook (7th Edition):

Layer, Jacob. “POLD2 Promotes Chromosomal Rearrangements and Inaccurate End-Joining in Human Cells.” 2019. Web. 20 Jan 2021.

Vancouver:

Layer J. POLD2 Promotes Chromosomal Rearrangements and Inaccurate End-Joining in Human Cells. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2021 Jan 20]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41121277.

Council of Science Editors:

Layer J. POLD2 Promotes Chromosomal Rearrangements and Inaccurate End-Joining in Human Cells. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41121277

20. Ballantyne, Maeve Kellett. Immune modulation in pigs through editing of the RELA locus.

Degree: PhD, 2017, University of Edinburgh

 Livestock animals are an ancient, vital renewable natural resource. Many livestock species have the ability to convert inedible crops and waste food into food fit… (more)

Subjects/Keywords: African swine fever; ASF; genome editing; RELA gene

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ballantyne, M. K. (2017). Immune modulation in pigs through editing of the RELA locus. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/28798

Chicago Manual of Style (16th Edition):

Ballantyne, Maeve Kellett. “Immune modulation in pigs through editing of the RELA locus.” 2017. Doctoral Dissertation, University of Edinburgh. Accessed January 20, 2021. http://hdl.handle.net/1842/28798.

MLA Handbook (7th Edition):

Ballantyne, Maeve Kellett. “Immune modulation in pigs through editing of the RELA locus.” 2017. Web. 20 Jan 2021.

Vancouver:

Ballantyne MK. Immune modulation in pigs through editing of the RELA locus. [Internet] [Doctoral dissertation]. University of Edinburgh; 2017. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1842/28798.

Council of Science Editors:

Ballantyne MK. Immune modulation in pigs through editing of the RELA locus. [Doctoral Dissertation]. University of Edinburgh; 2017. Available from: http://hdl.handle.net/1842/28798

21. Chowdhury, Rebecca. Insights into retinal cell fate determination in vertebrates using transcriptomic profiling and genome editing.

Degree: 2017, Iowa State University

 Deciphering the mechanisms of development of retinal neurons is not only of immense interest to developmental biologists, but is also vital for regenerative therapeutic applications.… (more)

Subjects/Keywords: Genome editing; Retina; Single cell transcriptomics; Developmental Biology; Genetics; Molecular Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chowdhury, R. (2017). Insights into retinal cell fate determination in vertebrates using transcriptomic profiling and genome editing. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16512

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):

Chowdhury, Rebecca. “Insights into retinal cell fate determination in vertebrates using transcriptomic profiling and genome editing.” 2017. Thesis, Iowa State University. Accessed January 20, 2021. https://lib.dr.iastate.edu/etd/16512.

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

MLA Handbook (7th Edition):

Chowdhury, Rebecca. “Insights into retinal cell fate determination in vertebrates using transcriptomic profiling and genome editing.” 2017. Web. 20 Jan 2021.

Vancouver:

Chowdhury R. Insights into retinal cell fate determination in vertebrates using transcriptomic profiling and genome editing. [Internet] [Thesis]. Iowa State University; 2017. [cited 2021 Jan 20]. Available from: https://lib.dr.iastate.edu/etd/16512.

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

Council of Science Editors:

Chowdhury R. Insights into retinal cell fate determination in vertebrates using transcriptomic profiling and genome editing. [Thesis]. Iowa State University; 2017. Available from: https://lib.dr.iastate.edu/etd/16512

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

22. Char, Si Nian. Development and utilization of genome editing tools in maize, sorghum and rice.

Degree: 2019, Iowa State University

Genome editing technologies have revolutionized the world of biology. Genome editing for site-specific genomic alterations started with engineered meganucleases, followed by programmable zinc finger nucleases… (more)

Subjects/Keywords: CRISPR/Cas9; genome editing; maize; rice; sorghum; TALENS; Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Char, S. N. (2019). Development and utilization of genome editing tools in maize, sorghum and rice. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16984

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):

Char, Si Nian. “Development and utilization of genome editing tools in maize, sorghum and rice.” 2019. Thesis, Iowa State University. Accessed January 20, 2021. https://lib.dr.iastate.edu/etd/16984.

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

MLA Handbook (7th Edition):

Char, Si Nian. “Development and utilization of genome editing tools in maize, sorghum and rice.” 2019. Web. 20 Jan 2021.

Vancouver:

Char SN. Development and utilization of genome editing tools in maize, sorghum and rice. [Internet] [Thesis]. Iowa State University; 2019. [cited 2021 Jan 20]. Available from: https://lib.dr.iastate.edu/etd/16984.

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

Council of Science Editors:

Char SN. Development and utilization of genome editing tools in maize, sorghum and rice. [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/16984

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


University of Washington

23. Findlay, Gregory. High-throughput interrogation of genome function and cellular lineage.

Degree: PhD, 2018, University of Washington

 Mutations can reveal how biological functions are encoded in our DNA, and how biological specimens relate to one another. In nature, mutations occur infrequently and… (more)

Subjects/Keywords: BRCA1; CRISPR; genetics; genome editing; lineage tracing; VUS; Genetics; Genetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Findlay, G. (2018). High-throughput interrogation of genome function and cellular lineage. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/41800

Chicago Manual of Style (16th Edition):

Findlay, Gregory. “High-throughput interrogation of genome function and cellular lineage.” 2018. Doctoral Dissertation, University of Washington. Accessed January 20, 2021. http://hdl.handle.net/1773/41800.

MLA Handbook (7th Edition):

Findlay, Gregory. “High-throughput interrogation of genome function and cellular lineage.” 2018. Web. 20 Jan 2021.

Vancouver:

Findlay G. High-throughput interrogation of genome function and cellular lineage. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1773/41800.

Council of Science Editors:

Findlay G. High-throughput interrogation of genome function and cellular lineage. [Doctoral Dissertation]. University of Washington; 2018. Available from: http://hdl.handle.net/1773/41800


University of Toronto

24. Mejdani, Marios. Anti-CRISPRs and CRISPR-Cas: Characterization and Biotechnology.

Degree: PhD, 2019, University of Toronto

Abstract Bacteria and phages (bacterial specific viruses) have been undergoing an evolutionary arms race for billions of years, whereby bacteria evolve mechanisms to inhibit phage… (more)

Subjects/Keywords: Anti-CRISPR; Bacteriophages; CRISPR-Cas; Gene regulation; Genome editing; 0487

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mejdani, M. (2019). Anti-CRISPRs and CRISPR-Cas: Characterization and Biotechnology. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/102773

Chicago Manual of Style (16th Edition):

Mejdani, Marios. “Anti-CRISPRs and CRISPR-Cas: Characterization and Biotechnology.” 2019. Doctoral Dissertation, University of Toronto. Accessed January 20, 2021. http://hdl.handle.net/1807/102773.

MLA Handbook (7th Edition):

Mejdani, Marios. “Anti-CRISPRs and CRISPR-Cas: Characterization and Biotechnology.” 2019. Web. 20 Jan 2021.

Vancouver:

Mejdani M. Anti-CRISPRs and CRISPR-Cas: Characterization and Biotechnology. [Internet] [Doctoral dissertation]. University of Toronto; 2019. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1807/102773.

Council of Science Editors:

Mejdani M. Anti-CRISPRs and CRISPR-Cas: Characterization and Biotechnology. [Doctoral Dissertation]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/102773


Virginia Tech

25. Perry, Justin Bradley. Novel approaches to treat mitochondrial complex-I mediated defects in disease.

Degree: PhD, Human Nutrition, Foods, and Exercise, 2019, Virginia Tech

 Dysfunction within complex I (CI) of the mitochondrial electron transport system has been implicated in a number of disease states ranging from cardiovascular diseases to… (more)

Subjects/Keywords: Mitochondria; Ischemia/Reperfusion; Mitochondrial Disease; Genome Editing; Idebenone

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Perry, J. B. (2019). Novel approaches to treat mitochondrial complex-I mediated defects in disease. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/100602

Chicago Manual of Style (16th Edition):

Perry, Justin Bradley. “Novel approaches to treat mitochondrial complex-I mediated defects in disease.” 2019. Doctoral Dissertation, Virginia Tech. Accessed January 20, 2021. http://hdl.handle.net/10919/100602.

MLA Handbook (7th Edition):

Perry, Justin Bradley. “Novel approaches to treat mitochondrial complex-I mediated defects in disease.” 2019. Web. 20 Jan 2021.

Vancouver:

Perry JB. Novel approaches to treat mitochondrial complex-I mediated defects in disease. [Internet] [Doctoral dissertation]. Virginia Tech; 2019. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10919/100602.

Council of Science Editors:

Perry JB. Novel approaches to treat mitochondrial complex-I mediated defects in disease. [Doctoral Dissertation]. Virginia Tech; 2019. Available from: http://hdl.handle.net/10919/100602


University of Minnesota

26. Dhande, Yogesh. Glycopolymers for Targeted Gene Delivery and Genome Editing.

Degree: PhD, Chemical Engineering, 2017, University of Minnesota

 Targeted delivery of therapeutics is of great interest to reduce toxicity and immunogenicity of the treatment. In particular, the liver is an ideal target for… (more)

Subjects/Keywords: Asialoglycoprotein receptor; Gene delivery; Genome editing; Glycopolymer; Liver targeting; Nanoparticle

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dhande, Y. (2017). Glycopolymers for Targeted Gene Delivery and Genome Editing. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/209051

Chicago Manual of Style (16th Edition):

Dhande, Yogesh. “Glycopolymers for Targeted Gene Delivery and Genome Editing.” 2017. Doctoral Dissertation, University of Minnesota. Accessed January 20, 2021. http://hdl.handle.net/11299/209051.

MLA Handbook (7th Edition):

Dhande, Yogesh. “Glycopolymers for Targeted Gene Delivery and Genome Editing.” 2017. Web. 20 Jan 2021.

Vancouver:

Dhande Y. Glycopolymers for Targeted Gene Delivery and Genome Editing. [Internet] [Doctoral dissertation]. University of Minnesota; 2017. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/11299/209051.

Council of Science Editors:

Dhande Y. Glycopolymers for Targeted Gene Delivery and Genome Editing. [Doctoral Dissertation]. University of Minnesota; 2017. Available from: http://hdl.handle.net/11299/209051

27. Garza, Johan. Efficient and Multiplex genome editing using GeneArt?? CRISPR Nuclease mRNA .

Degree: 2014, California State University – San Marcos

 CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) system is derived from a prokaryotic adaptive immune system that uses an RNA-guided DNA nuclease to mutate and… (more)

Subjects/Keywords: CRISPR; Cas9; GeneArt; Efficient; Multiplex; genome; editing; Nuclease; mRNA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Garza, J. (2014). Efficient and Multiplex genome editing using GeneArt?? CRISPR Nuclease mRNA . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.3/138870

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):

Garza, Johan. “Efficient and Multiplex genome editing using GeneArt?? CRISPR Nuclease mRNA .” 2014. Thesis, California State University – San Marcos. Accessed January 20, 2021. http://hdl.handle.net/10211.3/138870.

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

MLA Handbook (7th Edition):

Garza, Johan. “Efficient and Multiplex genome editing using GeneArt?? CRISPR Nuclease mRNA .” 2014. Web. 20 Jan 2021.

Vancouver:

Garza J. Efficient and Multiplex genome editing using GeneArt?? CRISPR Nuclease mRNA . [Internet] [Thesis]. California State University – San Marcos; 2014. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10211.3/138870.

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

Council of Science Editors:

Garza J. Efficient and Multiplex genome editing using GeneArt?? CRISPR Nuclease mRNA . [Thesis]. California State University – San Marcos; 2014. Available from: http://hdl.handle.net/10211.3/138870

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


Duke University

28. Thakore, Pratiksha Ishwarsinh. Targeted Gene Repression Technologies for Regenerative Medicine, Genomics, and Gene Therapy .

Degree: 2016, Duke University

  Gene regulation is a complex and tightly controlled process that defines cell function in physiological and abnormal states. Programmable gene repression technologies enable loss-of-function… (more)

Subjects/Keywords: Biomedical engineering; CRISPR/Cas9; Epigenome editing; Gene regulation; Genome engineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thakore, P. I. (2016). Targeted Gene Repression Technologies for Regenerative Medicine, Genomics, and Gene Therapy . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/12179

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):

Thakore, Pratiksha Ishwarsinh. “Targeted Gene Repression Technologies for Regenerative Medicine, Genomics, and Gene Therapy .” 2016. Thesis, Duke University. Accessed January 20, 2021. http://hdl.handle.net/10161/12179.

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

MLA Handbook (7th Edition):

Thakore, Pratiksha Ishwarsinh. “Targeted Gene Repression Technologies for Regenerative Medicine, Genomics, and Gene Therapy .” 2016. Web. 20 Jan 2021.

Vancouver:

Thakore PI. Targeted Gene Repression Technologies for Regenerative Medicine, Genomics, and Gene Therapy . [Internet] [Thesis]. Duke University; 2016. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10161/12179.

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

Council of Science Editors:

Thakore PI. Targeted Gene Repression Technologies for Regenerative Medicine, Genomics, and Gene Therapy . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/12179

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

29. Ferguson, Jack. Interaction of host and viral microRNAs with infectious laryngotracheitis virus transcripts.

Degree: PhD, 2019, University of Edinburgh

 Infectious Laryngotracheitis Virus (ILTV) is an Alphaherpesvirus of the domesticated chicken and other economically important fowl such as pheasants, peafowl and turkeys. It causes an… (more)

Subjects/Keywords: Infectious Laryngotracheitis; Infectious Laryngotracheitis Virus; microRNAs; 10 miRNAs; genome editing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ferguson, J. (2019). Interaction of host and viral microRNAs with infectious laryngotracheitis virus transcripts. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/35998

Chicago Manual of Style (16th Edition):

Ferguson, Jack. “Interaction of host and viral microRNAs with infectious laryngotracheitis virus transcripts.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed January 20, 2021. http://hdl.handle.net/1842/35998.

MLA Handbook (7th Edition):

Ferguson, Jack. “Interaction of host and viral microRNAs with infectious laryngotracheitis virus transcripts.” 2019. Web. 20 Jan 2021.

Vancouver:

Ferguson J. Interaction of host and viral microRNAs with infectious laryngotracheitis virus transcripts. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/1842/35998.

Council of Science Editors:

Ferguson J. Interaction of host and viral microRNAs with infectious laryngotracheitis virus transcripts. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/35998


Virginia Tech

30. Fang, Yufeng. Nuclear Localization of Proteins and Genome Editing in the Oomycete Phytophthora sojae.

Degree: PhD, Genetics, Bioinformatics, and Computational Biology, 2016, Virginia Tech

 Oomycetes are fungi-like eukaryotic microorganisms, which are actually phylogenetic relatives of diatoms and brown algae, within the kingdom Stramenopila. Many oomycete species, mainly in the… (more)

Subjects/Keywords: Oomycetes; Phytophthora sojae; nuclear localization signals; CRISPR/Cas9; genome editing

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fang, Y. (2016). Nuclear Localization of Proteins and Genome Editing in the Oomycete Phytophthora sojae. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/74232

Chicago Manual of Style (16th Edition):

Fang, Yufeng. “Nuclear Localization of Proteins and Genome Editing in the Oomycete Phytophthora sojae.” 2016. Doctoral Dissertation, Virginia Tech. Accessed January 20, 2021. http://hdl.handle.net/10919/74232.

MLA Handbook (7th Edition):

Fang, Yufeng. “Nuclear Localization of Proteins and Genome Editing in the Oomycete Phytophthora sojae.” 2016. Web. 20 Jan 2021.

Vancouver:

Fang Y. Nuclear Localization of Proteins and Genome Editing in the Oomycete Phytophthora sojae. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2021 Jan 20]. Available from: http://hdl.handle.net/10919/74232.

Council of Science Editors:

Fang Y. Nuclear Localization of Proteins and Genome Editing in the Oomycete Phytophthora sojae. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/74232

[1] [2] [3] [4] [5]

.