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You searched for subject:(CRISPR Cas9). Showing records 1 – 30 of 377 total matches.

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Texas A&M University

1. Morin, Andrew. Characterization of Cas9-Mediated microRNA Knockout.

Degree: MS, Biomedical Sciences, 2015, Texas A&M University

 MicroRNAs are short regulatory RNAs that primarily operate at the posttranscriptional level, acting as part of the RISC complex to destabilize mRNA prior to, or… (more)

Subjects/Keywords: CRISPR/Cas9; microRNA

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APA (6th Edition):

Morin, A. (2015). Characterization of Cas9-Mediated microRNA Knockout. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156200

Chicago Manual of Style (16th Edition):

Morin, Andrew. “Characterization of Cas9-Mediated microRNA Knockout.” 2015. Masters Thesis, Texas A&M University. Accessed October 31, 2020. http://hdl.handle.net/1969.1/156200.

MLA Handbook (7th Edition):

Morin, Andrew. “Characterization of Cas9-Mediated microRNA Knockout.” 2015. Web. 31 Oct 2020.

Vancouver:

Morin A. Characterization of Cas9-Mediated microRNA Knockout. [Internet] [Masters thesis]. Texas A&M University; 2015. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1969.1/156200.

Council of Science Editors:

Morin A. Characterization of Cas9-Mediated microRNA Knockout. [Masters Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156200


Rice University

2. Rivera Longsworth, Gia Francesca. Expanding the Enzymatic Activity of the Programmable Endonuclease Cas9.

Degree: MA, Natural Sciences, 2018, Rice University

 The CRISPR-Cas9 gene editing system has revolutionized our ability to make targeted mutations in a variety of organisms. In zebrafish, we are able to use… (more)

Subjects/Keywords: zebrafish; Cas9; CRISPR

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APA (6th Edition):

Rivera Longsworth, G. F. (2018). Expanding the Enzymatic Activity of the Programmable Endonuclease Cas9. (Masters Thesis). Rice University. Retrieved from http://hdl.handle.net/1911/105841

Chicago Manual of Style (16th Edition):

Rivera Longsworth, Gia Francesca. “Expanding the Enzymatic Activity of the Programmable Endonuclease Cas9.” 2018. Masters Thesis, Rice University. Accessed October 31, 2020. http://hdl.handle.net/1911/105841.

MLA Handbook (7th Edition):

Rivera Longsworth, Gia Francesca. “Expanding the Enzymatic Activity of the Programmable Endonuclease Cas9.” 2018. Web. 31 Oct 2020.

Vancouver:

Rivera Longsworth GF. Expanding the Enzymatic Activity of the Programmable Endonuclease Cas9. [Internet] [Masters thesis]. Rice University; 2018. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1911/105841.

Council of Science Editors:

Rivera Longsworth GF. Expanding the Enzymatic Activity of the Programmable Endonuclease Cas9. [Masters Thesis]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105841


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 October 31, 2020. http://hdl.handle.net/10063/8944.

MLA Handbook (7th Edition):

Upton, Jevon. “Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes.” 2020. Web. 31 Oct 2020.

Vancouver:

Upton J. Using Lentivirus and CRISPR to Modify Cattle Embryonic Genes. [Internet] [Masters thesis]. Victoria University of Wellington; 2020. [cited 2020 Oct 31]. 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


University of Cambridge

4. Turner, Gemma. Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities.

Degree: PhD, 2020, University of Cambridge

 The development of targeted therapies has had a significant impact on cancer survival rates. However, targeting cancers that are driven by loss of tumour suppressor… (more)

Subjects/Keywords: CRISPR/Cas9; iPSCs; Cancer

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APA (6th Edition):

Turner, G. (2020). Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/303478https://www.repository.cam.ac.uk/bitstream/1810/303478/2/AppendixA.1_Oligonucleotide_sequences.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/3/AppendixA.2_Mass_spectrometry_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/4/AppendixA.3_NeoR-IRES_library_backbone.dna ; https://www.repository.cam.ac.uk/bitstream/1810/303478/5/AppendixA.4_gRNA_library_read%20counts.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/6/AppendixA.5_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/7/AppendixA.6_Scaled_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/8/AppendixA.7_MAGeCK_depletion_values_for_iPSC%20screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/9/AppendixA.8_Biological_replicate_overlaps.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/10/AppendixA.9_KO-specific_depleted_genes.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/11/AppendixA.10_MAGeCK_enrichment_values_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/12/AppendixA.11_PBAF-BAF_mutant_cancer_cell_lines.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/13/AppendixA.12_Sanger_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/14/AppendixA.13_Broad_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/15/AppendixA.14_Candidate_PBAF-BAF_gene_SLIs.txt

Chicago Manual of Style (16th Edition):

Turner, Gemma. “Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://www.repository.cam.ac.uk/handle/1810/303478https://www.repository.cam.ac.uk/bitstream/1810/303478/2/AppendixA.1_Oligonucleotide_sequences.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/3/AppendixA.2_Mass_spectrometry_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/4/AppendixA.3_NeoR-IRES_library_backbone.dna ; https://www.repository.cam.ac.uk/bitstream/1810/303478/5/AppendixA.4_gRNA_library_read%20counts.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/6/AppendixA.5_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/7/AppendixA.6_Scaled_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/8/AppendixA.7_MAGeCK_depletion_values_for_iPSC%20screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/9/AppendixA.8_Biological_replicate_overlaps.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/10/AppendixA.9_KO-specific_depleted_genes.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/11/AppendixA.10_MAGeCK_enrichment_values_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/12/AppendixA.11_PBAF-BAF_mutant_cancer_cell_lines.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/13/AppendixA.12_Sanger_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/14/AppendixA.13_Broad_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/15/AppendixA.14_Candidate_PBAF-BAF_gene_SLIs.txt.

MLA Handbook (7th Edition):

Turner, Gemma. “Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities.” 2020. Web. 31 Oct 2020.

Vancouver:

Turner G. Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 31]. Available from: https://www.repository.cam.ac.uk/handle/1810/303478https://www.repository.cam.ac.uk/bitstream/1810/303478/2/AppendixA.1_Oligonucleotide_sequences.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/3/AppendixA.2_Mass_spectrometry_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/4/AppendixA.3_NeoR-IRES_library_backbone.dna ; https://www.repository.cam.ac.uk/bitstream/1810/303478/5/AppendixA.4_gRNA_library_read%20counts.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/6/AppendixA.5_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/7/AppendixA.6_Scaled_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/8/AppendixA.7_MAGeCK_depletion_values_for_iPSC%20screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/9/AppendixA.8_Biological_replicate_overlaps.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/10/AppendixA.9_KO-specific_depleted_genes.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/11/AppendixA.10_MAGeCK_enrichment_values_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/12/AppendixA.11_PBAF-BAF_mutant_cancer_cell_lines.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/13/AppendixA.12_Sanger_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/14/AppendixA.13_Broad_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/15/AppendixA.14_Candidate_PBAF-BAF_gene_SLIs.txt.

Council of Science Editors:

Turner G. Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/303478https://www.repository.cam.ac.uk/bitstream/1810/303478/2/AppendixA.1_Oligonucleotide_sequences.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/3/AppendixA.2_Mass_spectrometry_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/4/AppendixA.3_NeoR-IRES_library_backbone.dna ; https://www.repository.cam.ac.uk/bitstream/1810/303478/5/AppendixA.4_gRNA_library_read%20counts.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/6/AppendixA.5_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/7/AppendixA.6_Scaled_Bayes_Factors_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/8/AppendixA.7_MAGeCK_depletion_values_for_iPSC%20screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/9/AppendixA.8_Biological_replicate_overlaps.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/10/AppendixA.9_KO-specific_depleted_genes.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/11/AppendixA.10_MAGeCK_enrichment_values_for_iPSC_screens.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/12/AppendixA.11_PBAF-BAF_mutant_cancer_cell_lines.xlsx ; https://www.repository.cam.ac.uk/bitstream/1810/303478/13/AppendixA.12_Sanger_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/14/AppendixA.13_Broad_Institute_screen_data.txt ; https://www.repository.cam.ac.uk/bitstream/1810/303478/15/AppendixA.14_Candidate_PBAF-BAF_gene_SLIs.txt


University of Cambridge

5. Garland, Sarah. Exploring Non-transgenic CRISPR-Cas9 gRNA Delivery Using Transactivation in Nicotiana benthamiana.

Degree: PhD, 2020, University of Cambridge

 Gene editing via CRISPR-Cas9 (Clustered, Regularly Interspaced, Short Palindromic Repeats – CRISPR-associated protein 9) is a powerful tool in biotechnology. The method involves an endonuclease… (more)

Subjects/Keywords: gene editing; CRISPR-Cas9; plants

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

APA (6th Edition):

Garland, S. (2020). Exploring Non-transgenic CRISPR-Cas9 gRNA Delivery Using Transactivation in Nicotiana benthamiana. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/301828

Chicago Manual of Style (16th Edition):

Garland, Sarah. “Exploring Non-transgenic CRISPR-Cas9 gRNA Delivery Using Transactivation in Nicotiana benthamiana.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://www.repository.cam.ac.uk/handle/1810/301828.

MLA Handbook (7th Edition):

Garland, Sarah. “Exploring Non-transgenic CRISPR-Cas9 gRNA Delivery Using Transactivation in Nicotiana benthamiana.” 2020. Web. 31 Oct 2020.

Vancouver:

Garland S. Exploring Non-transgenic CRISPR-Cas9 gRNA Delivery Using Transactivation in Nicotiana benthamiana. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 31]. Available from: https://www.repository.cam.ac.uk/handle/1810/301828.

Council of Science Editors:

Garland S. Exploring Non-transgenic CRISPR-Cas9 gRNA Delivery Using Transactivation in Nicotiana benthamiana. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/301828


Colorado School of Mines

6. Vogler, Brian W. Development of CRISPR/Cas9 in Nannochloropsis and other algae toward understanding and manipulating energy allocation.

Degree: PhD, Chemistry, 2018, Colorado School of Mines

 Nannochloropsis is a genus of eukaryotic microalgae that grows well in outdoor bioreactors and produces high yields of triacylglycerols (TAGs), which can be processed into… (more)

Subjects/Keywords: Bioengineering; Cas9; Algae; CRISPR; Carbohydrate

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APA (6th Edition):

Vogler, B. W. (2018). Development of CRISPR/Cas9 in Nannochloropsis and other algae toward understanding and manipulating energy allocation. (Doctoral Dissertation). Colorado School of Mines. Retrieved from http://hdl.handle.net/11124/172561

Chicago Manual of Style (16th Edition):

Vogler, Brian W. “Development of CRISPR/Cas9 in Nannochloropsis and other algae toward understanding and manipulating energy allocation.” 2018. Doctoral Dissertation, Colorado School of Mines. Accessed October 31, 2020. http://hdl.handle.net/11124/172561.

MLA Handbook (7th Edition):

Vogler, Brian W. “Development of CRISPR/Cas9 in Nannochloropsis and other algae toward understanding and manipulating energy allocation.” 2018. Web. 31 Oct 2020.

Vancouver:

Vogler BW. Development of CRISPR/Cas9 in Nannochloropsis and other algae toward understanding and manipulating energy allocation. [Internet] [Doctoral dissertation]. Colorado School of Mines; 2018. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/11124/172561.

Council of Science Editors:

Vogler BW. Development of CRISPR/Cas9 in Nannochloropsis and other algae toward understanding and manipulating energy allocation. [Doctoral Dissertation]. Colorado School of Mines; 2018. Available from: http://hdl.handle.net/11124/172561


University of Cambridge

7. Turner, Gemma. Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities.

Degree: PhD, 2020, University of Cambridge

 The development of targeted therapies has had a significant impact on cancer survival rates. However, targeting cancers that are driven by loss of tumour suppressor… (more)

Subjects/Keywords: CRISPR/Cas9; iPSCs; Cancer

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

APA (6th Edition):

Turner, G. (2020). Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.50566 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801883

Chicago Manual of Style (16th Edition):

Turner, Gemma. “Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://doi.org/10.17863/CAM.50566 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801883.

MLA Handbook (7th Edition):

Turner, Gemma. “Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities.” 2020. Web. 31 Oct 2020.

Vancouver:

Turner G. Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 31]. Available from: https://doi.org/10.17863/CAM.50566 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801883.

Council of Science Editors:

Turner G. Application of CRISPR/Cas9 screening to study cancer drivers and to identify novel cancer vulnerabilities. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://doi.org/10.17863/CAM.50566 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801883


University of Cambridge

8. Garland, Sarah. Exploring non-transgenic CRISPR-Cas9 gRNA delivery using transactivation in Nicotiana benthamiana.

Degree: PhD, 2020, University of Cambridge

 Gene editing via CRISPR-Cas9 (Clustered, Regularly Interspaced, Short Palindromic Repeats – CRISPR-associated protein 9) is a powerful tool in biotechnology. The method involves an endonuclease… (more)

Subjects/Keywords: gene editing; CRISPR-Cas9; plants

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

APA (6th Edition):

Garland, S. (2020). Exploring non-transgenic CRISPR-Cas9 gRNA delivery using transactivation in Nicotiana benthamiana. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.48896 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801747

Chicago Manual of Style (16th Edition):

Garland, Sarah. “Exploring non-transgenic CRISPR-Cas9 gRNA delivery using transactivation in Nicotiana benthamiana.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://doi.org/10.17863/CAM.48896 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801747.

MLA Handbook (7th Edition):

Garland, Sarah. “Exploring non-transgenic CRISPR-Cas9 gRNA delivery using transactivation in Nicotiana benthamiana.” 2020. Web. 31 Oct 2020.

Vancouver:

Garland S. Exploring non-transgenic CRISPR-Cas9 gRNA delivery using transactivation in Nicotiana benthamiana. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 31]. Available from: https://doi.org/10.17863/CAM.48896 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801747.

Council of Science Editors:

Garland S. Exploring non-transgenic CRISPR-Cas9 gRNA delivery using transactivation in Nicotiana benthamiana. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://doi.org/10.17863/CAM.48896 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801747


Texas A&M University

9. 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

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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 October 31, 2020. 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. 31 Oct 2020.

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 2020 Oct 31]. 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

10. Tsarmpopoulos, Iason. Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools.

Degree: Docteur es, Microbiologie - immunologie, 2017, Bordeaux

Les mycoplasmes sont des bactéries pathogènes, dotées de petits génomes d’environ 1Mbp, avec une faible teneur en G+C. L'intérêt de la communauté scientifique pour ces… (more)

Subjects/Keywords: Biologie de synthèse; CRISPR/Cas9; Mycoplasma; Synthetic Biology; CRISPR/Cas9; Mycoplasma

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APA (6th Edition):

Tsarmpopoulos, I. (2017). Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2017BORD0787

Chicago Manual of Style (16th Edition):

Tsarmpopoulos, Iason. “Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools.” 2017. Doctoral Dissertation, Bordeaux. Accessed October 31, 2020. http://www.theses.fr/2017BORD0787.

MLA Handbook (7th Edition):

Tsarmpopoulos, Iason. “Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools.” 2017. Web. 31 Oct 2020.

Vancouver:

Tsarmpopoulos I. Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools. [Internet] [Doctoral dissertation]. Bordeaux; 2017. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2017BORD0787.

Council of Science Editors:

Tsarmpopoulos I. Ingénierie de génome de bactéries minimales par des outils CRISPR/Cas9 : Engineering the genome of minimal bacteria using CRISPR/Cas9 tools. [Doctoral Dissertation]. Bordeaux; 2017. Available from: http://www.theses.fr/2017BORD0787

11. Raas, Quentin. Inactivation génique des transporteurs ABC peroxysomaux ABCD1 et ABCD2 dans les cellules microgliales BV-2 : étude de la physiopathogenèse de l’adrénoleucodystrophie liée à l’X. : Inactivation of peroxisomal ABC transporters, ABCD1 and ABCD2 in BV-2 microglial cells : Towards a better understanding of X-linked adrenoleukodystrophy.

Degree: Docteur es, Biochimie et biologie moléculaire, 2018, Bourgogne Franche-Comté

L’adrénoleucodystrophie liée à l’X (X-ALD) est une maladie neurodégénérative sévère caractérisée par une accumulation d’acides gras à très longue chaîne (AGTLC), conséquence d’un défaut de… (more)

Subjects/Keywords: CRISPR-Cas9; Peroxysome; Abcd1; Microglie; Microglia; Abcd1; Peroxisome; CRISPR-Cas9; 571.6

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

APA (6th Edition):

Raas, Q. (2018). Inactivation génique des transporteurs ABC peroxysomaux ABCD1 et ABCD2 dans les cellules microgliales BV-2 : étude de la physiopathogenèse de l’adrénoleucodystrophie liée à l’X. : Inactivation of peroxisomal ABC transporters, ABCD1 and ABCD2 in BV-2 microglial cells : Towards a better understanding of X-linked adrenoleukodystrophy. (Doctoral Dissertation). Bourgogne Franche-Comté. Retrieved from http://www.theses.fr/2018UBFCI011

Chicago Manual of Style (16th Edition):

Raas, Quentin. “Inactivation génique des transporteurs ABC peroxysomaux ABCD1 et ABCD2 dans les cellules microgliales BV-2 : étude de la physiopathogenèse de l’adrénoleucodystrophie liée à l’X. : Inactivation of peroxisomal ABC transporters, ABCD1 and ABCD2 in BV-2 microglial cells : Towards a better understanding of X-linked adrenoleukodystrophy.” 2018. Doctoral Dissertation, Bourgogne Franche-Comté. Accessed October 31, 2020. http://www.theses.fr/2018UBFCI011.

MLA Handbook (7th Edition):

Raas, Quentin. “Inactivation génique des transporteurs ABC peroxysomaux ABCD1 et ABCD2 dans les cellules microgliales BV-2 : étude de la physiopathogenèse de l’adrénoleucodystrophie liée à l’X. : Inactivation of peroxisomal ABC transporters, ABCD1 and ABCD2 in BV-2 microglial cells : Towards a better understanding of X-linked adrenoleukodystrophy.” 2018. Web. 31 Oct 2020.

Vancouver:

Raas Q. Inactivation génique des transporteurs ABC peroxysomaux ABCD1 et ABCD2 dans les cellules microgliales BV-2 : étude de la physiopathogenèse de l’adrénoleucodystrophie liée à l’X. : Inactivation of peroxisomal ABC transporters, ABCD1 and ABCD2 in BV-2 microglial cells : Towards a better understanding of X-linked adrenoleukodystrophy. [Internet] [Doctoral dissertation]. Bourgogne Franche-Comté; 2018. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2018UBFCI011.

Council of Science Editors:

Raas Q. Inactivation génique des transporteurs ABC peroxysomaux ABCD1 et ABCD2 dans les cellules microgliales BV-2 : étude de la physiopathogenèse de l’adrénoleucodystrophie liée à l’X. : Inactivation of peroxisomal ABC transporters, ABCD1 and ABCD2 in BV-2 microglial cells : Towards a better understanding of X-linked adrenoleukodystrophy. [Doctoral Dissertation]. Bourgogne Franche-Comté; 2018. Available from: http://www.theses.fr/2018UBFCI011

12. Parrot, Camila. Création d'un système rapporteur pour l'étude de mutations de p53 : Creating a reporter system for the analysis of p53 mutations.

Degree: Docteur es, Génétique, 2016, Bordeaux

Le cancer est responsable de plus de 15% des décès. L’activation d’oncogènes et l’inactivation de gènes suppresseurs de tumeur contribuent à la transformation des cellules.… (more)

Subjects/Keywords: Cancer; P53; TALEN; CRISPR-Cas9; Cancer; P53; TALEN; CRISPR-Cas9

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APA (6th Edition):

Parrot, C. (2016). Création d'un système rapporteur pour l'étude de mutations de p53 : Creating a reporter system for the analysis of p53 mutations. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2016BORD0198

Chicago Manual of Style (16th Edition):

Parrot, Camila. “Création d'un système rapporteur pour l'étude de mutations de p53 : Creating a reporter system for the analysis of p53 mutations.” 2016. Doctoral Dissertation, Bordeaux. Accessed October 31, 2020. http://www.theses.fr/2016BORD0198.

MLA Handbook (7th Edition):

Parrot, Camila. “Création d'un système rapporteur pour l'étude de mutations de p53 : Creating a reporter system for the analysis of p53 mutations.” 2016. Web. 31 Oct 2020.

Vancouver:

Parrot C. Création d'un système rapporteur pour l'étude de mutations de p53 : Creating a reporter system for the analysis of p53 mutations. [Internet] [Doctoral dissertation]. Bordeaux; 2016. [cited 2020 Oct 31]. Available from: http://www.theses.fr/2016BORD0198.

Council of Science Editors:

Parrot C. Création d'un système rapporteur pour l'étude de mutations de p53 : Creating a reporter system for the analysis of p53 mutations. [Doctoral Dissertation]. Bordeaux; 2016. Available from: http://www.theses.fr/2016BORD0198


University of California – San Diego

13. Lotfy, Peter. Elucidating the role of autophagy in the clearance of phosphorylated tau protein in human neurons.

Degree: Biology, 2016, University of California – San Diego

 More than 40 million people world-wide suffer from tauopathies–neurodegenerative diseases in which the aggregation of microtubule-associated protein tau into intracellular inclusions is a core pathology.… (more)

Subjects/Keywords: Biology; Alzheimer's; autophagy; Cas9; CRISPR; neuroscience; tau

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APA (6th Edition):

Lotfy, P. (2016). Elucidating the role of autophagy in the clearance of phosphorylated tau protein in human neurons. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/854345k3

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):

Lotfy, Peter. “Elucidating the role of autophagy in the clearance of phosphorylated tau protein in human neurons.” 2016. Thesis, University of California – San Diego. Accessed October 31, 2020. http://www.escholarship.org/uc/item/854345k3.

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

MLA Handbook (7th Edition):

Lotfy, Peter. “Elucidating the role of autophagy in the clearance of phosphorylated tau protein in human neurons.” 2016. Web. 31 Oct 2020.

Vancouver:

Lotfy P. Elucidating the role of autophagy in the clearance of phosphorylated tau protein in human neurons. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/854345k3.

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

Council of Science Editors:

Lotfy P. Elucidating the role of autophagy in the clearance of phosphorylated tau protein in human neurons. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/854345k3

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


University of California – San Diego

14. Plouffe, Steven W. Characterization of Hippo pathway regulation and the physiological implications of its downstream effectors YAP and TAZ.

Degree: Biomedical Sciences, 2018, University of California – San Diego

 The Hippo pathway and its downstream effectors, transcriptional coactivators YAP and TAZ, are important for regulating tissue homeostasis and their dysregulation has been implicated in… (more)

Subjects/Keywords: Pharmacology; CRISPR/Cas9; Hippo pathway; TAZ; YAP

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APA (6th Edition):

Plouffe, S. W. (2018). Characterization of Hippo pathway regulation and the physiological implications of its downstream effectors YAP and TAZ. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/15k9q60f

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):

Plouffe, Steven W. “Characterization of Hippo pathway regulation and the physiological implications of its downstream effectors YAP and TAZ.” 2018. Thesis, University of California – San Diego. Accessed October 31, 2020. http://www.escholarship.org/uc/item/15k9q60f.

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

MLA Handbook (7th Edition):

Plouffe, Steven W. “Characterization of Hippo pathway regulation and the physiological implications of its downstream effectors YAP and TAZ.” 2018. Web. 31 Oct 2020.

Vancouver:

Plouffe SW. Characterization of Hippo pathway regulation and the physiological implications of its downstream effectors YAP and TAZ. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/15k9q60f.

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

Council of Science Editors:

Plouffe SW. Characterization of Hippo pathway regulation and the physiological implications of its downstream effectors YAP and TAZ. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/15k9q60f

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


University of California – Berkeley

15. Limsirichai, Prajit. Reactivating Latent HIV-1.

Degree: Microbiology, 2016, University of California – Berkeley

 Complete eradication of HIV-1 infection is impeded by the existence of cells that harbor chromosomally integrated but transcriptionally inactive provirus. These latently-infected cells can persist… (more)

Subjects/Keywords: Virology; CRISPR/Cas9; HIV-1; latency; reactivation

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APA (6th Edition):

Limsirichai, P. (2016). Reactivating Latent HIV-1. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2hn437qt

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):

Limsirichai, Prajit. “Reactivating Latent HIV-1.” 2016. Thesis, University of California – Berkeley. Accessed October 31, 2020. http://www.escholarship.org/uc/item/2hn437qt.

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

MLA Handbook (7th Edition):

Limsirichai, Prajit. “Reactivating Latent HIV-1.” 2016. Web. 31 Oct 2020.

Vancouver:

Limsirichai P. Reactivating Latent HIV-1. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/2hn437qt.

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

Council of Science Editors:

Limsirichai P. Reactivating Latent HIV-1. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/2hn437qt

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


Harvard University

16. 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

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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 October 31, 2020. 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. 31 Oct 2020.

Vancouver:

Lin C. Characterization and Optimization of the CRISPR/Cas System for Applications in Genome Engineering. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Oct 31]. 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

17. Hanamirian, Michael Albert. ANALYZING THE POTENTIAL IMPACT AND ETHICAL QUESTIONS SURROUNDING CRISPR-CAS9 IN EMBRYONIC GENOME EDITING.

Degree: 2018, Wake Forest University

 Analyzing Potential Impact and Ethical Questions Concerning CRISPR-Cas9 in Genome Editing covers the current state of genome editing, and more specifically, the CRISPR-Cas9 system. The… (more)

Subjects/Keywords: CRISPR-Cas9

…perhaps changing society as we know it forever: CRISPR-Cas9 genome editing. Why the topic of… …genome editing? In brief,11 the CRISPR-Cas9 system is found exclusively in prokaryotic… …12 CRISPR stands for clustered regularly interspaced short palindromic repeats while Cas9… …are many reasons why successfully harnessing CRISPR-Cas9 would be the single most important… …advancement in modern medicine. CRISPR-Cas9 could be used on the somatic cells of humans to fight… 

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APA (6th Edition):

Hanamirian, M. A. (2018). ANALYZING THE POTENTIAL IMPACT AND ETHICAL QUESTIONS SURROUNDING CRISPR-CAS9 IN EMBRYONIC GENOME EDITING. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/90762

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):

Hanamirian, Michael Albert. “ANALYZING THE POTENTIAL IMPACT AND ETHICAL QUESTIONS SURROUNDING CRISPR-CAS9 IN EMBRYONIC GENOME EDITING.” 2018. Thesis, Wake Forest University. Accessed October 31, 2020. http://hdl.handle.net/10339/90762.

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

MLA Handbook (7th Edition):

Hanamirian, Michael Albert. “ANALYZING THE POTENTIAL IMPACT AND ETHICAL QUESTIONS SURROUNDING CRISPR-CAS9 IN EMBRYONIC GENOME EDITING.” 2018. Web. 31 Oct 2020.

Vancouver:

Hanamirian MA. ANALYZING THE POTENTIAL IMPACT AND ETHICAL QUESTIONS SURROUNDING CRISPR-CAS9 IN EMBRYONIC GENOME EDITING. [Internet] [Thesis]. Wake Forest University; 2018. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10339/90762.

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

Council of Science Editors:

Hanamirian MA. ANALYZING THE POTENTIAL IMPACT AND ETHICAL QUESTIONS SURROUNDING CRISPR-CAS9 IN EMBRYONIC GENOME EDITING. [Thesis]. Wake Forest University; 2018. Available from: http://hdl.handle.net/10339/90762

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


University of Connecticut

18. Rosiene, Joel. Astrocytic Expansion in a Model of Neurofibromatosis 1 (NF1) Deficiency.

Degree: MS, Physiology and Neurobiology, 2015, University of Connecticut

  Neurofibramatosis type 1 is an autosomal dominant disorder characterized by the development of both benign and malignant neoplasms of glial origin, as well as… (more)

Subjects/Keywords: NF1 Development IUE Neurofibromatosis CRISPR/Cas9

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APA (6th Edition):

Rosiene, J. (2015). Astrocytic Expansion in a Model of Neurofibromatosis 1 (NF1) Deficiency. (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/800

Chicago Manual of Style (16th Edition):

Rosiene, Joel. “Astrocytic Expansion in a Model of Neurofibromatosis 1 (NF1) Deficiency.” 2015. Masters Thesis, University of Connecticut. Accessed October 31, 2020. https://opencommons.uconn.edu/gs_theses/800.

MLA Handbook (7th Edition):

Rosiene, Joel. “Astrocytic Expansion in a Model of Neurofibromatosis 1 (NF1) Deficiency.” 2015. Web. 31 Oct 2020.

Vancouver:

Rosiene J. Astrocytic Expansion in a Model of Neurofibromatosis 1 (NF1) Deficiency. [Internet] [Masters thesis]. University of Connecticut; 2015. [cited 2020 Oct 31]. Available from: https://opencommons.uconn.edu/gs_theses/800.

Council of Science Editors:

Rosiene J. Astrocytic Expansion in a Model of Neurofibromatosis 1 (NF1) Deficiency. [Masters Thesis]. University of Connecticut; 2015. Available from: https://opencommons.uconn.edu/gs_theses/800


Harvard University

19. Najm, Fadi John. Combinatorial Genetic Screening in Cancer.

Degree: PhD, 2019, Harvard University

Chromatin-modifying enzymes impact cell state and function. They are frequently mutated in disease, including many cancers, and present promising opportunities for therapeutic intervention. These enzymes… (more)

Subjects/Keywords: Cancer; genetics; chromatin; CRISPR-Cas9; synthetic lethal

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APA (6th Edition):

Najm, F. J. (2019). Combinatorial Genetic Screening in Cancer. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029799

Chicago Manual of Style (16th Edition):

Najm, Fadi John. “Combinatorial Genetic Screening in Cancer.” 2019. Doctoral Dissertation, Harvard University. Accessed October 31, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029799.

MLA Handbook (7th Edition):

Najm, Fadi John. “Combinatorial Genetic Screening in Cancer.” 2019. Web. 31 Oct 2020.

Vancouver:

Najm FJ. Combinatorial Genetic Screening in Cancer. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2020 Oct 31]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029799.

Council of Science Editors:

Najm FJ. Combinatorial Genetic Screening in Cancer. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029799


Kansas State University

20. Kakeshpour, Tayebeh. Tomato class II glutaredoxin mutants generated via multiplex CRISPR/Cas9 genome editing technology are susceptible to multiple abiotic stresses.

Degree: PhD, Department of Horticulture and Natural Resources, 2020, Kansas State University

 Gene silencing technologies such as clustered regulatory short palindromic repeats (CRISPR)/Cas9 and RNA interference (RNAi) created a revolution in genome engineering. They are highly site-specific,… (more)

Subjects/Keywords: Abiotic Stress; CRISPR/Cas9; Glutaredoxin; Tomato

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APA (6th Edition):

Kakeshpour, T. (2020). Tomato class II glutaredoxin mutants generated via multiplex CRISPR/Cas9 genome editing technology are susceptible to multiple abiotic stresses. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/40823

Chicago Manual of Style (16th Edition):

Kakeshpour, Tayebeh. “Tomato class II glutaredoxin mutants generated via multiplex CRISPR/Cas9 genome editing technology are susceptible to multiple abiotic stresses.” 2020. Doctoral Dissertation, Kansas State University. Accessed October 31, 2020. http://hdl.handle.net/2097/40823.

MLA Handbook (7th Edition):

Kakeshpour, Tayebeh. “Tomato class II glutaredoxin mutants generated via multiplex CRISPR/Cas9 genome editing technology are susceptible to multiple abiotic stresses.” 2020. Web. 31 Oct 2020.

Vancouver:

Kakeshpour T. Tomato class II glutaredoxin mutants generated via multiplex CRISPR/Cas9 genome editing technology are susceptible to multiple abiotic stresses. [Internet] [Doctoral dissertation]. Kansas State University; 2020. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/2097/40823.

Council of Science Editors:

Kakeshpour T. Tomato class II glutaredoxin mutants generated via multiplex CRISPR/Cas9 genome editing technology are susceptible to multiple abiotic stresses. [Doctoral Dissertation]. Kansas State University; 2020. Available from: http://hdl.handle.net/2097/40823


University of California – San Diego

21. Glazer, Colby W. CRISPR/Cas9 in Saccharomyces cerevisiae and Its Application to Promote Future Scientists.

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

 Middle school and high school students are often confronted with the problem of textbook memorization as the singular form of biological learning, rather than acquiring… (more)

Subjects/Keywords: Biology; Biochemistry; Molecular biology; Cas9; CRISPR

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APA (6th Edition):

Glazer, C. W. (2018). CRISPR/Cas9 in Saccharomyces cerevisiae and Its Application to Promote Future Scientists. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0js5q7dp

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):

Glazer, Colby W. “CRISPR/Cas9 in Saccharomyces cerevisiae and Its Application to Promote Future Scientists.” 2018. Thesis, University of California – San Diego. Accessed October 31, 2020. http://www.escholarship.org/uc/item/0js5q7dp.

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

MLA Handbook (7th Edition):

Glazer, Colby W. “CRISPR/Cas9 in Saccharomyces cerevisiae and Its Application to Promote Future Scientists.” 2018. Web. 31 Oct 2020.

Vancouver:

Glazer CW. CRISPR/Cas9 in Saccharomyces cerevisiae and Its Application to Promote Future Scientists. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Oct 31]. Available from: http://www.escholarship.org/uc/item/0js5q7dp.

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

Council of Science Editors:

Glazer CW. CRISPR/Cas9 in Saccharomyces cerevisiae and Its Application to Promote Future Scientists. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/0js5q7dp

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


University of Cambridge

22. Hadi, Fazal. Understanding the Cancer Resistance Mechanisms of the Naked Mole-Rat.

Degree: PhD, 2020, University of Cambridge

 The naked mole-rat (NMR, Heterocephalus glaber) is a highly unusual mammal: eusocial, cold-blooded and with remarkable resistance to hypoxia, hypercapnia and acid-induced pain. Furthermore, NMRs… (more)

Subjects/Keywords: Naked Mole-Rat; Cancer Resistance; CRISPR-Cas9

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APA (6th Edition):

Hadi, F. (2020). Understanding the Cancer Resistance Mechanisms of the Naked Mole-Rat. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/303395

Chicago Manual of Style (16th Edition):

Hadi, Fazal. “Understanding the Cancer Resistance Mechanisms of the Naked Mole-Rat.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://www.repository.cam.ac.uk/handle/1810/303395.

MLA Handbook (7th Edition):

Hadi, Fazal. “Understanding the Cancer Resistance Mechanisms of the Naked Mole-Rat.” 2020. Web. 31 Oct 2020.

Vancouver:

Hadi F. Understanding the Cancer Resistance Mechanisms of the Naked Mole-Rat. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 31]. Available from: https://www.repository.cam.ac.uk/handle/1810/303395.

Council of Science Editors:

Hadi F. Understanding the Cancer Resistance Mechanisms of the Naked Mole-Rat. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/303395


York University

23. 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

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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 October 31, 2020. 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. 31 Oct 2020.

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 2020 Oct 31]. 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


Tampere University

24. Hetemäki, Saara. Targeting QTLs using the CRISPR/Cas9 system in yeast .

Degree: 2017, Tampere University

 Background and objectives: There is still limited knowledge about how phenotypes arise from genetic loci. It is especially difficult to understand complex traits that are… (more)

Subjects/Keywords: CRISPR/Cas9; genetic engineering; QTL; S. cerevisiae

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

APA (6th Edition):

Hetemäki, S. (2017). Targeting QTLs using the CRISPR/Cas9 system in yeast . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/101294

Chicago Manual of Style (16th Edition):

Hetemäki, Saara. “Targeting QTLs using the CRISPR/Cas9 system in yeast .” 2017. Masters Thesis, Tampere University. Accessed October 31, 2020. https://trepo.tuni.fi/handle/10024/101294.

MLA Handbook (7th Edition):

Hetemäki, Saara. “Targeting QTLs using the CRISPR/Cas9 system in yeast .” 2017. Web. 31 Oct 2020.

Vancouver:

Hetemäki S. Targeting QTLs using the CRISPR/Cas9 system in yeast . [Internet] [Masters thesis]. Tampere University; 2017. [cited 2020 Oct 31]. Available from: https://trepo.tuni.fi/handle/10024/101294.

Council of Science Editors:

Hetemäki S. Targeting QTLs using the CRISPR/Cas9 system in yeast . [Masters Thesis]. Tampere University; 2017. Available from: https://trepo.tuni.fi/handle/10024/101294


University of Houston

25. Anthony-Gonda, Kim 1980-. Genetically Reprogramming Immune Modulatory Activity in Cancer Cells using TALE and CRISPR/Cas9 Technologies.

Degree: PhD, Biochemistry, 2014, University of Houston

 The advent of TALE and CRISPR/Cas9 technologies has ushered in an era of new genome-engineering tools to precisely manipulate the human genome. These tools hold… (more)

Subjects/Keywords: Genome-engineering; TALE technology; CRISPR/Cas9 technology

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APA (6th Edition):

Anthony-Gonda, K. 1. (2014). Genetically Reprogramming Immune Modulatory Activity in Cancer Cells using TALE and CRISPR/Cas9 Technologies. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/1904

Chicago Manual of Style (16th Edition):

Anthony-Gonda, Kim 1980-. “Genetically Reprogramming Immune Modulatory Activity in Cancer Cells using TALE and CRISPR/Cas9 Technologies.” 2014. Doctoral Dissertation, University of Houston. Accessed October 31, 2020. http://hdl.handle.net/10657/1904.

MLA Handbook (7th Edition):

Anthony-Gonda, Kim 1980-. “Genetically Reprogramming Immune Modulatory Activity in Cancer Cells using TALE and CRISPR/Cas9 Technologies.” 2014. Web. 31 Oct 2020.

Vancouver:

Anthony-Gonda K1. Genetically Reprogramming Immune Modulatory Activity in Cancer Cells using TALE and CRISPR/Cas9 Technologies. [Internet] [Doctoral dissertation]. University of Houston; 2014. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/10657/1904.

Council of Science Editors:

Anthony-Gonda K1. Genetically Reprogramming Immune Modulatory Activity in Cancer Cells using TALE and CRISPR/Cas9 Technologies. [Doctoral Dissertation]. University of Houston; 2014. Available from: http://hdl.handle.net/10657/1904


University of Debrecen

26. Jebudánszki, Vivien. CRISPR CAS9 alapú genomszerkesztő technológiák alkalmazása a sejtvonal fejlesztésben .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 A diplomamunkámba a CRISPR Cas9 alapú genomszerkesztő technológiák alkalmazását mutattam be a sejtvonal fejlesztés területén közben egy kevés betekintést nyújtottam a sejttenyészet, plazmid klónozás, izolálás,… (more)

Subjects/Keywords: genomszerkesztés; CRISPR Cas9

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

APA (6th Edition):

Jebudánszki, V. (n.d.). CRISPR CAS9 alapú genomszerkesztő technológiák alkalmazása a sejtvonal fejlesztésben . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/234988

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jebudánszki, Vivien. “CRISPR CAS9 alapú genomszerkesztő technológiák alkalmazása a sejtvonal fejlesztésben .” Thesis, University of Debrecen. Accessed October 31, 2020. http://hdl.handle.net/2437/234988.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jebudánszki, Vivien. “CRISPR CAS9 alapú genomszerkesztő technológiák alkalmazása a sejtvonal fejlesztésben .” Web. 31 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Jebudánszki V. CRISPR CAS9 alapú genomszerkesztő technológiák alkalmazása a sejtvonal fejlesztésben . [Internet] [Thesis]. University of Debrecen; [cited 2020 Oct 31]. Available from: http://hdl.handle.net/2437/234988.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Jebudánszki V. CRISPR CAS9 alapú genomszerkesztő technológiák alkalmazása a sejtvonal fejlesztésben . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/234988

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Brigham Young University

27. Kempton, Colton E. The Effects of Nucleosome Positioning and Chromatin Architecture on Transgene Expression.

Degree: PhD, 2017, Brigham Young University

 Eukaryotes use proteins to carefully package and compact their genomes to fit into the nuclei of their individual cells. Nucleosomes are the primary level of… (more)

Subjects/Keywords: nucleosome; CRISPR/Cas9; Caenorhabditis elegans; Microbiology

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APA (6th Edition):

Kempton, C. E. (2017). The Effects of Nucleosome Positioning and Chromatin Architecture on Transgene Expression. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7463&context=etd

Chicago Manual of Style (16th Edition):

Kempton, Colton E. “The Effects of Nucleosome Positioning and Chromatin Architecture on Transgene Expression.” 2017. Doctoral Dissertation, Brigham Young University. Accessed October 31, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7463&context=etd.

MLA Handbook (7th Edition):

Kempton, Colton E. “The Effects of Nucleosome Positioning and Chromatin Architecture on Transgene Expression.” 2017. Web. 31 Oct 2020.

Vancouver:

Kempton CE. The Effects of Nucleosome Positioning and Chromatin Architecture on Transgene Expression. [Internet] [Doctoral dissertation]. Brigham Young University; 2017. [cited 2020 Oct 31]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7463&context=etd.

Council of Science Editors:

Kempton CE. The Effects of Nucleosome Positioning and Chromatin Architecture on Transgene Expression. [Doctoral Dissertation]. Brigham Young University; 2017. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7463&context=etd

28. Kosicki, Michal Konrad. Cas9-induced on-target genomic damage.

Degree: PhD, 2019, University of Cambridge

CRISPR/Cas9 is the gene editing tool of choice in basic research and poised to become one in clinical context. However, current studies on the topic… (more)

Subjects/Keywords: CRISPR; DNA damage repair; Cas9; mutagenesis

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

APA (6th Edition):

Kosicki, M. K. (2019). Cas9-induced on-target genomic damage. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/289911

Chicago Manual of Style (16th Edition):

Kosicki, Michal Konrad. “Cas9-induced on-target genomic damage.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 31, 2020. https://www.repository.cam.ac.uk/handle/1810/289911.

MLA Handbook (7th Edition):

Kosicki, Michal Konrad. “Cas9-induced on-target genomic damage.” 2019. Web. 31 Oct 2020.

Vancouver:

Kosicki MK. Cas9-induced on-target genomic damage. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 31]. Available from: https://www.repository.cam.ac.uk/handle/1810/289911.

Council of Science Editors:

Kosicki MK. Cas9-induced on-target genomic damage. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/289911


University of Toronto

29. Thavalingam, Annoj. The Functional Characterization of Anti-CRISPR AcrIIC2Nme.

Degree: 2019, University of Toronto

The CRISPR-Cas system is a prokaryotic adaptive immune system that provides protection against foreign genetic elements, such as bacteriophages. Phages have thus evolved a set… (more)

Subjects/Keywords: anti-CRISPR; Bacteria; Cas9; Protein; 0487

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APA (6th Edition):

Thavalingam, A. (2019). The Functional Characterization of Anti-CRISPR AcrIIC2Nme. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/98383

Chicago Manual of Style (16th Edition):

Thavalingam, Annoj. “The Functional Characterization of Anti-CRISPR AcrIIC2Nme.” 2019. Masters Thesis, University of Toronto. Accessed October 31, 2020. http://hdl.handle.net/1807/98383.

MLA Handbook (7th Edition):

Thavalingam, Annoj. “The Functional Characterization of Anti-CRISPR AcrIIC2Nme.” 2019. Web. 31 Oct 2020.

Vancouver:

Thavalingam A. The Functional Characterization of Anti-CRISPR AcrIIC2Nme. [Internet] [Masters thesis]. University of Toronto; 2019. [cited 2020 Oct 31]. Available from: http://hdl.handle.net/1807/98383.

Council of Science Editors:

Thavalingam A. The Functional Characterization of Anti-CRISPR AcrIIC2Nme. [Masters Thesis]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/98383

30. Welker, Jordan Michael. Application of precise genome editing tools in the zebrafish model to elucidate protein function with regards to developmental phenotypes.

Degree: 2019, Iowa State University

 Genetic engineering is a powerful tool for biologists and geneticists to study the natural world. In general, it allows for asking and answering precise gene… (more)

Subjects/Keywords: CRISPR/Cas9; Genetic engineering; Synthetic Alleles; Genetics

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

APA (6th Edition):

Welker, J. M. (2019). Application of precise genome editing tools in the zebrafish model to elucidate protein function with regards to developmental phenotypes. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/17121

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):

Welker, Jordan Michael. “Application of precise genome editing tools in the zebrafish model to elucidate protein function with regards to developmental phenotypes.” 2019. Thesis, Iowa State University. Accessed October 31, 2020. https://lib.dr.iastate.edu/etd/17121.

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

MLA Handbook (7th Edition):

Welker, Jordan Michael. “Application of precise genome editing tools in the zebrafish model to elucidate protein function with regards to developmental phenotypes.” 2019. Web. 31 Oct 2020.

Vancouver:

Welker JM. Application of precise genome editing tools in the zebrafish model to elucidate protein function with regards to developmental phenotypes. [Internet] [Thesis]. Iowa State University; 2019. [cited 2020 Oct 31]. Available from: https://lib.dr.iastate.edu/etd/17121.

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

Council of Science Editors:

Welker JM. Application of precise genome editing tools in the zebrafish model to elucidate protein function with regards to developmental phenotypes. [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/17121

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

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