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You searched for subject:(genetic screens). Showing records 1 – 19 of 19 total matches.

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1. Zaini, Muhammad Nazhif Bin. Endogenous Reporter Systems for High-Throughput Functional Screening in Clear Cell Renal Cell Carcinoma.

Degree: PhD, 2019, University of Cambridge

 Tissue-specific transcriptional programs define cancer phenotypes. However, the molecular mechanism behind the transcriptional specificity is mostly unknown, hindering the development of therapeutic approaches. In clear… (more)

Subjects/Keywords: Genetic Screens; ccRCC; Endogenous Reporters; HIF2A

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

APA (6th Edition):

Zaini, M. N. B. (2019). Endogenous Reporter Systems for High-Throughput Functional Screening in Clear Cell Renal Cell Carcinoma. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/294122

Chicago Manual of Style (16th Edition):

Zaini, Muhammad Nazhif Bin. “Endogenous Reporter Systems for High-Throughput Functional Screening in Clear Cell Renal Cell Carcinoma.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 19, 2021. https://www.repository.cam.ac.uk/handle/1810/294122.

MLA Handbook (7th Edition):

Zaini, Muhammad Nazhif Bin. “Endogenous Reporter Systems for High-Throughput Functional Screening in Clear Cell Renal Cell Carcinoma.” 2019. Web. 19 Jan 2021.

Vancouver:

Zaini MNB. Endogenous Reporter Systems for High-Throughput Functional Screening in Clear Cell Renal Cell Carcinoma. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Jan 19]. Available from: https://www.repository.cam.ac.uk/handle/1810/294122.

Council of Science Editors:

Zaini MNB. Endogenous Reporter Systems for High-Throughput Functional Screening in Clear Cell Renal Cell Carcinoma. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/294122

2. Edokpolo, Anthony Omorodion. Screen for Suppressors and Enhancers of Excitotoxic Neurodegeneration.

Degree: MS(M.S.), Biology, 2014, City University of New York

  Excitotoxicity is an important and frequently observed neurodegenerative process. Excitotoxicity mediates brain damage in a range of diseases and conditions including stroke, and is… (more)

Subjects/Keywords: Excitotoxicity; genetic screens; neurodegeneration; Biology; Cell and Developmental Biology

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APA (6th Edition):

Edokpolo, A. O. (2014). Screen for Suppressors and Enhancers of Excitotoxic Neurodegeneration. (Thesis). City University of New York. Retrieved from https://academicworks.cuny.edu/cc_etds_theses/516

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):

Edokpolo, Anthony Omorodion. “Screen for Suppressors and Enhancers of Excitotoxic Neurodegeneration.” 2014. Thesis, City University of New York. Accessed January 19, 2021. https://academicworks.cuny.edu/cc_etds_theses/516.

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

MLA Handbook (7th Edition):

Edokpolo, Anthony Omorodion. “Screen for Suppressors and Enhancers of Excitotoxic Neurodegeneration.” 2014. Web. 19 Jan 2021.

Vancouver:

Edokpolo AO. Screen for Suppressors and Enhancers of Excitotoxic Neurodegeneration. [Internet] [Thesis]. City University of New York; 2014. [cited 2021 Jan 19]. Available from: https://academicworks.cuny.edu/cc_etds_theses/516.

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

Council of Science Editors:

Edokpolo AO. Screen for Suppressors and Enhancers of Excitotoxic Neurodegeneration. [Thesis]. City University of New York; 2014. Available from: https://academicworks.cuny.edu/cc_etds_theses/516

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


University of Cambridge

3. Dickson, Anna. Regulation of Protein Degradation at the Endoplasmic Reticulum.

Degree: PhD, 2020, University of Cambridge

 Endoplasmic reticulum (ER) associated degradation (ERAD) is important for removing damaged or misfolded proteins at the ER membrane, and is central to the physiological regulation… (more)

Subjects/Keywords: Endoplasmic reticulum; protein degradation; Cholesterol synthesis; Hypoxia; CRISPR Cas9 genetic screens

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APA (6th Edition):

Dickson, A. (2020). Regulation of Protein Degradation at the Endoplasmic Reticulum. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/312261

Chicago Manual of Style (16th Edition):

Dickson, Anna. “Regulation of Protein Degradation at the Endoplasmic Reticulum.” 2020. Doctoral Dissertation, University of Cambridge. Accessed January 19, 2021. https://www.repository.cam.ac.uk/handle/1810/312261.

MLA Handbook (7th Edition):

Dickson, Anna. “Regulation of Protein Degradation at the Endoplasmic Reticulum.” 2020. Web. 19 Jan 2021.

Vancouver:

Dickson A. Regulation of Protein Degradation at the Endoplasmic Reticulum. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 Jan 19]. Available from: https://www.repository.cam.ac.uk/handle/1810/312261.

Council of Science Editors:

Dickson A. Regulation of Protein Degradation at the Endoplasmic Reticulum. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/312261

4. le Sage, Carlos Karel. Identifying cancer-causing noncoding RNAs.

Degree: 2008, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 To circumvent the dependency on prediction models, we developed a microRNA-screen-based assay to establish links between cellular phenotypes and microRNAs (miRNAs). To this end, a… (more)

Subjects/Keywords: Genetic screens; MicroRNA; Noncoding RNA; Genetic screens; MicroRNA; Noncoding RNA

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APA (6th Edition):

le Sage, C. K. (2008). Identifying cancer-causing noncoding RNAs. (Doctoral Dissertation). Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/12553

Chicago Manual of Style (16th Edition):

le Sage, Carlos Karel. “Identifying cancer-causing noncoding RNAs.” 2008. Doctoral Dissertation, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed January 19, 2021. http://hdl.handle.net/1887/12553.

MLA Handbook (7th Edition):

le Sage, Carlos Karel. “Identifying cancer-causing noncoding RNAs.” 2008. Web. 19 Jan 2021.

Vancouver:

le Sage CK. Identifying cancer-causing noncoding RNAs. [Internet] [Doctoral dissertation]. Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2008. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1887/12553.

Council of Science Editors:

le Sage CK. Identifying cancer-causing noncoding RNAs. [Doctoral Dissertation]. Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2008. Available from: http://hdl.handle.net/1887/12553


University of California – Berkeley

5. Gowen, Benjamin Gregory. Regulation and Genetic Manipulation of Ligands for the Immunoreceptor NKG2D.

Degree: Molecular & Cell Biology, 2015, University of California – Berkeley

 NKG2D is an important activating receptor expressed by natural killer (NK) cells and some subsets of T cells. NKG2D recognizes a family of cell surface… (more)

Subjects/Keywords: Immunology; Alternative mRNA splicing; Cellular stress; CRISPR/Cas9; Forward genetic screens; NKG2D; Tumor immunology

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APA (6th Edition):

Gowen, B. G. (2015). Regulation and Genetic Manipulation of Ligands for the Immunoreceptor NKG2D. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/1vz119f1

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):

Gowen, Benjamin Gregory. “Regulation and Genetic Manipulation of Ligands for the Immunoreceptor NKG2D.” 2015. Thesis, University of California – Berkeley. Accessed January 19, 2021. http://www.escholarship.org/uc/item/1vz119f1.

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

MLA Handbook (7th Edition):

Gowen, Benjamin Gregory. “Regulation and Genetic Manipulation of Ligands for the Immunoreceptor NKG2D.” 2015. Web. 19 Jan 2021.

Vancouver:

Gowen BG. Regulation and Genetic Manipulation of Ligands for the Immunoreceptor NKG2D. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2021 Jan 19]. Available from: http://www.escholarship.org/uc/item/1vz119f1.

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

Council of Science Editors:

Gowen BG. Regulation and Genetic Manipulation of Ligands for the Immunoreceptor NKG2D. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/1vz119f1

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


University of Pennsylvania

6. Drake, Mary Jane. Uncovering Bunyavirus-Host Interactions.

Degree: 2016, University of Pennsylvania

 Bunyaviruses are a large family of enveloped RNA viruses that are distributed globally and include many important human and agricultural pathogens. Compared with other pathogenic… (more)

Subjects/Keywords: bunyavirus; hantavirus; haploid genetic screens; phlebovirus; virus; virus entry; Cell Biology; Virology

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APA (6th Edition):

Drake, M. J. (2016). Uncovering Bunyavirus-Host Interactions. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1691

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):

Drake, Mary Jane. “Uncovering Bunyavirus-Host Interactions.” 2016. Thesis, University of Pennsylvania. Accessed January 19, 2021. https://repository.upenn.edu/edissertations/1691.

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

MLA Handbook (7th Edition):

Drake, Mary Jane. “Uncovering Bunyavirus-Host Interactions.” 2016. Web. 19 Jan 2021.

Vancouver:

Drake MJ. Uncovering Bunyavirus-Host Interactions. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2021 Jan 19]. Available from: https://repository.upenn.edu/edissertations/1691.

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

Council of Science Editors:

Drake MJ. Uncovering Bunyavirus-Host Interactions. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/1691

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


University of Lund

7. Galeev, Roman. Identification of intrinsic regulators in normal and malignant human hematopoiesis. An RNA-interference approach.

Degree: 2018, University of Lund

 Bildandet av blodceller, hematopoesen, utgår från ett litet antal av de så kallade hematopoetiska stamceller som sitter i vår benmärg. Dessa celler har förmågan att… (more)

Subjects/Keywords: Hematology; hematopoietic stem cell; RNA interference; Acute myeloid leukemia; myelodysplastic syndrome; genetic screens; next generation sequencing; genetic regulators

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APA (6th Edition):

Galeev, R. (2018). Identification of intrinsic regulators in normal and malignant human hematopoiesis. An RNA-interference approach. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/04e4dc27-4903-4350-a588-b80eb8e6b941 ; https://portal.research.lu.se/ws/files/49805781/Roman_Galeev_thesis_only.pdf

Chicago Manual of Style (16th Edition):

Galeev, Roman. “Identification of intrinsic regulators in normal and malignant human hematopoiesis. An RNA-interference approach.” 2018. Doctoral Dissertation, University of Lund. Accessed January 19, 2021. https://lup.lub.lu.se/record/04e4dc27-4903-4350-a588-b80eb8e6b941 ; https://portal.research.lu.se/ws/files/49805781/Roman_Galeev_thesis_only.pdf.

MLA Handbook (7th Edition):

Galeev, Roman. “Identification of intrinsic regulators in normal and malignant human hematopoiesis. An RNA-interference approach.” 2018. Web. 19 Jan 2021.

Vancouver:

Galeev R. Identification of intrinsic regulators in normal and malignant human hematopoiesis. An RNA-interference approach. [Internet] [Doctoral dissertation]. University of Lund; 2018. [cited 2021 Jan 19]. Available from: https://lup.lub.lu.se/record/04e4dc27-4903-4350-a588-b80eb8e6b941 ; https://portal.research.lu.se/ws/files/49805781/Roman_Galeev_thesis_only.pdf.

Council of Science Editors:

Galeev R. Identification of intrinsic regulators in normal and malignant human hematopoiesis. An RNA-interference approach. [Doctoral Dissertation]. University of Lund; 2018. Available from: https://lup.lub.lu.se/record/04e4dc27-4903-4350-a588-b80eb8e6b941 ; https://portal.research.lu.se/ws/files/49805781/Roman_Galeev_thesis_only.pdf

8. Brunen, Diede. Improving cancer therapy through unraveling drug resistance.

Degree: 2017, University Utrecht

 The discovery that the growth and/or survival of cancer cells is dependent on certain oncogenic drivers — also described as ‘oncogene addiction’ — provided a… (more)

Subjects/Keywords: targeted therapy; drug resistance; genetic screens; biomarkers; combination therapies

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APA (6th Edition):

Brunen, D. (2017). Improving cancer therapy through unraveling drug resistance. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; http://dspace.library.uu.nl/handle/1874/354501

Chicago Manual of Style (16th Edition):

Brunen, Diede. “Improving cancer therapy through unraveling drug resistance.” 2017. Doctoral Dissertation, University Utrecht. Accessed January 19, 2021. http://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; http://dspace.library.uu.nl/handle/1874/354501.

MLA Handbook (7th Edition):

Brunen, Diede. “Improving cancer therapy through unraveling drug resistance.” 2017. Web. 19 Jan 2021.

Vancouver:

Brunen D. Improving cancer therapy through unraveling drug resistance. [Internet] [Doctoral dissertation]. University Utrecht; 2017. [cited 2021 Jan 19]. Available from: http://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; http://dspace.library.uu.nl/handle/1874/354501.

Council of Science Editors:

Brunen D. Improving cancer therapy through unraveling drug resistance. [Doctoral Dissertation]. University Utrecht; 2017. Available from: http://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; http://dspace.library.uu.nl/handle/1874/354501


University of Cambridge

9. Sharma, Sumana. Genome-scale identification of cellular pathways required for cell surface recognition.

Degree: PhD, 2018, University of Cambridge

 A range of biochemically diverse molecules located in the plasma membrane— such as proteins, glycans, and lipids—mediate cellular recognition events, initiation of signalling pathways, and… (more)

Subjects/Keywords: CRISPR-Cas9; Low-affinity interaction; Cellular-signalling; Loss-of-function genetic screens; Glycoseaminoglycans; Receptor-ligand interactions; GABA receptor

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APA (6th Edition):

Sharma, S. (2018). Genome-scale identification of cellular pathways required for cell surface recognition. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/271825

Chicago Manual of Style (16th Edition):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 19, 2021. https://www.repository.cam.ac.uk/handle/1810/271825.

MLA Handbook (7th Edition):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition.” 2018. Web. 19 Jan 2021.

Vancouver:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 19]. Available from: https://www.repository.cam.ac.uk/handle/1810/271825.

Council of Science Editors:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/271825

10. Brunen, Diede. Improving cancer therapy through unraveling drug resistance.

Degree: 2017, University Utrecht

 The discovery that the growth and/or survival of cancer cells is dependent on certain oncogenic drivers — also described as ‘oncogene addiction’ — provided a… (more)

Subjects/Keywords: targeted therapy; drug resistance; genetic screens; biomarkers; combination therapies

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APA (6th Edition):

Brunen, D. (2017). Improving cancer therapy through unraveling drug resistance. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; https://dspace.library.uu.nl/handle/1874/354501

Chicago Manual of Style (16th Edition):

Brunen, Diede. “Improving cancer therapy through unraveling drug resistance.” 2017. Doctoral Dissertation, University Utrecht. Accessed January 19, 2021. https://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; https://dspace.library.uu.nl/handle/1874/354501.

MLA Handbook (7th Edition):

Brunen, Diede. “Improving cancer therapy through unraveling drug resistance.” 2017. Web. 19 Jan 2021.

Vancouver:

Brunen D. Improving cancer therapy through unraveling drug resistance. [Internet] [Doctoral dissertation]. University Utrecht; 2017. [cited 2021 Jan 19]. Available from: https://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; https://dspace.library.uu.nl/handle/1874/354501.

Council of Science Editors:

Brunen D. Improving cancer therapy through unraveling drug resistance. [Doctoral Dissertation]. University Utrecht; 2017. Available from: https://dspace.library.uu.nl/handle/1874/354501 ; URN:NBN:NL:UI:10-1874-354501 ; urn:isbn:978-94-6233-691-9 ; URN:NBN:NL:UI:10-1874-354501 ; https://dspace.library.uu.nl/handle/1874/354501

11. Liao, Sida. A Genetic Interaction Analysis Identifies Novel Cancer Driver Modifiers and a Combination Therapy.

Degree: PhD, 2019, Harvard University

A large number of cancer drivers have been identified through tumor sequencing efforts but how they interact and the degree to which they can substitute… (more)

Subjects/Keywords: Cancer biology; Genetic screens; Drug resistance

…the biological function of these putative cancer drivers. Genetic Screens for Cancer Driver… …prior knowledge of the potential candidates, geneticists use forward genetic screens. The… …of the major tools currently used in forward genetic screens is described as follows. RNA… …non-mutagenic manner (38), further expanding its application in genetic screens… …Reading Frame screen To date, functional genetic screens have largely been done using a LOF… 

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APA (6th Edition):

Liao, S. (2019). A Genetic Interaction Analysis Identifies Novel Cancer Driver Modifiers and a Combination Therapy. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029794

Chicago Manual of Style (16th Edition):

Liao, Sida. “A Genetic Interaction Analysis Identifies Novel Cancer Driver Modifiers and a Combination Therapy.” 2019. Doctoral Dissertation, Harvard University. Accessed January 19, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029794.

MLA Handbook (7th Edition):

Liao, Sida. “A Genetic Interaction Analysis Identifies Novel Cancer Driver Modifiers and a Combination Therapy.” 2019. Web. 19 Jan 2021.

Vancouver:

Liao S. A Genetic Interaction Analysis Identifies Novel Cancer Driver Modifiers and a Combination Therapy. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2021 Jan 19]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029794.

Council of Science Editors:

Liao S. A Genetic Interaction Analysis Identifies Novel Cancer Driver Modifiers and a Combination Therapy. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029794

12. Zaini, Muhammad Nazhif Bin. Endogenous reporter systems for high-throughput functional screening in clear cell renal cell carcinoma.

Degree: PhD, 2019, University of Cambridge

 Tissue-specific transcriptional programs define cancer phenotypes. However, the molecular mechanism behind the transcriptional specificity is mostly unknown, hindering the development of therapeutic approaches. In clear… (more)

Subjects/Keywords: Genetic Screens; ccRCC; Endogenous Reporters; HIF2A

genetic screens as shown from an sgRNA -1- enrichment experiment that highlighted sgRNAs… …H2AmC fluorescent reporter systems for high-throughput genetic interrogation to delineate the… …systems for high-throughput genetic screening. 6.6 Conclusion REFERENCES 137-159 vii LIST… …lowest risk of developing metastases53,54,56. The genetic feature most closely associated with… …this risk65–67. Genetic predisposition for RCC risk exist in the form of family history of… 

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APA (6th Edition):

Zaini, M. N. B. (2019). Endogenous reporter systems for high-throughput functional screening in clear cell renal cell carcinoma. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.41223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782880

Chicago Manual of Style (16th Edition):

Zaini, Muhammad Nazhif Bin. “Endogenous reporter systems for high-throughput functional screening in clear cell renal cell carcinoma.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 19, 2021. https://doi.org/10.17863/CAM.41223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782880.

MLA Handbook (7th Edition):

Zaini, Muhammad Nazhif Bin. “Endogenous reporter systems for high-throughput functional screening in clear cell renal cell carcinoma.” 2019. Web. 19 Jan 2021.

Vancouver:

Zaini MNB. Endogenous reporter systems for high-throughput functional screening in clear cell renal cell carcinoma. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Jan 19]. Available from: https://doi.org/10.17863/CAM.41223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782880.

Council of Science Editors:

Zaini MNB. Endogenous reporter systems for high-throughput functional screening in clear cell renal cell carcinoma. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.41223 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782880


University of Cambridge

13. Sharma, Sumana. Genome-scale identification of cellular pathways required for cell surface recognition.

Degree: PhD, 2018, University of Cambridge

 A range of biochemically diverse molecules located in the plasma membrane— such as proteins, glycans, and lipids—mediate cellular recognition events, initiation of signalling pathways, and… (more)

Subjects/Keywords: 571.6; CRISPR-Cas9; Low-affinity interaction; Cellular-signalling; Loss-of-function genetic screens; Glycoseaminoglycans; Receptor-ligand interactions; GABA receptor

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APA (6th Edition):

Sharma, S. (2018). Genome-scale identification of cellular pathways required for cell surface recognition. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.18823 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744513

Chicago Manual of Style (16th Edition):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 19, 2021. https://doi.org/10.17863/CAM.18823 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744513.

MLA Handbook (7th Edition):

Sharma, Sumana. “Genome-scale identification of cellular pathways required for cell surface recognition.” 2018. Web. 19 Jan 2021.

Vancouver:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 19]. Available from: https://doi.org/10.17863/CAM.18823 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744513.

Council of Science Editors:

Sharma S. Genome-scale identification of cellular pathways required for cell surface recognition. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.18823 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744513


The Ohio State University

14. McWhorter, Michelle L. Development and analysis of a Zebrafish model of spinal muscular atrophy.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2005, The Ohio State University

 Spinal muscular atrophy (SMA) is an autosomal recessive disorder characterized by a loss of alpha-motoneurons in the spinal cord. SMA is caused by low levels… (more)

Subjects/Keywords: Biology, Molecular; SMA; SMN; motoneuron; zebrafish; reverse genetic screens

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APA (6th Edition):

McWhorter, M. L. (2005). Development and analysis of a Zebrafish model of spinal muscular atrophy. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1133212697

Chicago Manual of Style (16th Edition):

McWhorter, Michelle L. “Development and analysis of a Zebrafish model of spinal muscular atrophy.” 2005. Doctoral Dissertation, The Ohio State University. Accessed January 19, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1133212697.

MLA Handbook (7th Edition):

McWhorter, Michelle L. “Development and analysis of a Zebrafish model of spinal muscular atrophy.” 2005. Web. 19 Jan 2021.

Vancouver:

McWhorter ML. Development and analysis of a Zebrafish model of spinal muscular atrophy. [Internet] [Doctoral dissertation]. The Ohio State University; 2005. [cited 2021 Jan 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1133212697.

Council of Science Editors:

McWhorter ML. Development and analysis of a Zebrafish model of spinal muscular atrophy. [Doctoral Dissertation]. The Ohio State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1133212697

15. Reynolds, Mollie Megan. Identification of Novel Virulence Genes of Salmonella enterica Using an Array Based Analysis of Cistrons Under Selection.

Degree: PhD, Genetics, 2011, Texas A&M University

 Pools of mutants of minimal complexity but maximal coverage of genes of interest facilitate screening for genes under selection in a particular environment. Prior to… (more)

Subjects/Keywords: ABACUS; Salmonella; genetic screens; Twin arginine transport; motility

…Salmonella Genetic Screens: A Review ....................................... Problems with… …analyze pathways necessary for a particular process. Forward genetic screens, and now functional… …Genetic Screens: A Review In Vivo Expression Screens: IVET Promoter trap strategies were first… …be attributed to the differences in genetic make-up of each strain, however, this is only a… …and describe advances in forward genetic and functional genomic approaches that are… 

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APA (6th Edition):

Reynolds, M. M. (2011). Identification of Novel Virulence Genes of Salmonella enterica Using an Array Based Analysis of Cistrons Under Selection. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7675

Chicago Manual of Style (16th Edition):

Reynolds, Mollie Megan. “Identification of Novel Virulence Genes of Salmonella enterica Using an Array Based Analysis of Cistrons Under Selection.” 2011. Doctoral Dissertation, Texas A&M University. Accessed January 19, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7675.

MLA Handbook (7th Edition):

Reynolds, Mollie Megan. “Identification of Novel Virulence Genes of Salmonella enterica Using an Array Based Analysis of Cistrons Under Selection.” 2011. Web. 19 Jan 2021.

Vancouver:

Reynolds MM. Identification of Novel Virulence Genes of Salmonella enterica Using an Array Based Analysis of Cistrons Under Selection. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7675.

Council of Science Editors:

Reynolds MM. Identification of Novel Virulence Genes of Salmonella enterica Using an Array Based Analysis of Cistrons Under Selection. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7675

16. Pavlova, Natalya Nickolayevna. A Role for PVRL4-Driven Cell-Cell Interactions in Tumorigenesis.

Degree: PhD, Biological Chemistry and Molecular Pharmacology, 2012, Harvard University

 Deciphering genetic determinants of tumorigenesis is the greatest challenge and promise of the present-day era of biomedical research. As extensive tumor genome characterization efforts of… (more)

Subjects/Keywords: Genetics; anchorage independence; cancer; genetic screens; oncogene; transformation

…variety of biological phenotypes as a potential readout. Genetic screens with tumor-derived cDNA… …creating a whole-genome tool for performing gain-offunction genetic screens in mammalian systems… …mammalian cells. Logical frameworks are guiding the design of genetic screens Newly available… …decade, mammalian genetic screens have proven their utility as a 17 tool of systematic… …when designing genetic screens. Several of such frameworks could be isolated among those… 

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APA (6th Edition):

Pavlova, N. N. (2012). A Role for PVRL4-Driven Cell-Cell Interactions in Tumorigenesis. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:10423841

Chicago Manual of Style (16th Edition):

Pavlova, Natalya Nickolayevna. “A Role for PVRL4-Driven Cell-Cell Interactions in Tumorigenesis.” 2012. Doctoral Dissertation, Harvard University. Accessed January 19, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:10423841.

MLA Handbook (7th Edition):

Pavlova, Natalya Nickolayevna. “A Role for PVRL4-Driven Cell-Cell Interactions in Tumorigenesis.” 2012. Web. 19 Jan 2021.

Vancouver:

Pavlova NN. A Role for PVRL4-Driven Cell-Cell Interactions in Tumorigenesis. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2021 Jan 19]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10423841.

Council of Science Editors:

Pavlova NN. A Role for PVRL4-Driven Cell-Cell Interactions in Tumorigenesis. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10423841


Leiden University

17. Mezzadra, R. Genetic manipulation and genetic-based dissection of tumor-specific immunity.

Degree: 2019, Leiden University

 In this thesis I have firstly applied gene transfer technologies to the redirection of T cell specificity, by trying to overcome limitations related to non-viral… (more)

Subjects/Keywords: PD-L1; T cells; genetic screens; transposon-mediated gene-transfer; SLFN11; IFN-gamma; TCR; PD-L1; T cells; genetic screens; transposon-mediated gene-transfer; SLFN11; IFN-gamma; TCR

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APA (6th Edition):

Mezzadra, R. (2019). Genetic manipulation and genetic-based dissection of tumor-specific immunity. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/68811

Chicago Manual of Style (16th Edition):

Mezzadra, R. “Genetic manipulation and genetic-based dissection of tumor-specific immunity.” 2019. Doctoral Dissertation, Leiden University. Accessed January 19, 2021. http://hdl.handle.net/1887/68811.

MLA Handbook (7th Edition):

Mezzadra, R. “Genetic manipulation and genetic-based dissection of tumor-specific immunity.” 2019. Web. 19 Jan 2021.

Vancouver:

Mezzadra R. Genetic manipulation and genetic-based dissection of tumor-specific immunity. [Internet] [Doctoral dissertation]. Leiden University; 2019. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1887/68811.

Council of Science Editors:

Mezzadra R. Genetic manipulation and genetic-based dissection of tumor-specific immunity. [Doctoral Dissertation]. Leiden University; 2019. Available from: http://hdl.handle.net/1887/68811


Université Paris-Sud – Paris XI

18. Pellentz-Lemattre, Céline. Etude de la plasticité du protéasome : identification et caractérisation de cibles et de régulateurs : Study of proteasome plasticity : identification and characterization of targets and regulators.

Degree: Docteur es, Biologie, 2014, Université Paris-Sud – Paris XI

Le protéasome est une protéase multimérique essentielle et hautement conservée au cours de l’évolution. Le protéasome 26S eucaryote est l’unité catalytique du système Ubiquitine-Protéasome et… (more)

Subjects/Keywords: Protéasome; Saccharomyces cerevisiae; Cribles d’interactants physiques et génétiques; Logiciel R; Assemblage; Quiescence; Activité; Point de contrôle; Proteasome; Saccharomyces cerevisiae; Screens of physical and genetic interactors; R software; Assembly; Quiescence; Activity; Checkpoint

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APA (6th Edition):

Pellentz-Lemattre, C. (2014). Etude de la plasticité du protéasome : identification et caractérisation de cibles et de régulateurs : Study of proteasome plasticity : identification and characterization of targets and regulators. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA112128

Chicago Manual of Style (16th Edition):

Pellentz-Lemattre, Céline. “Etude de la plasticité du protéasome : identification et caractérisation de cibles et de régulateurs : Study of proteasome plasticity : identification and characterization of targets and regulators.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 19, 2021. http://www.theses.fr/2014PA112128.

MLA Handbook (7th Edition):

Pellentz-Lemattre, Céline. “Etude de la plasticité du protéasome : identification et caractérisation de cibles et de régulateurs : Study of proteasome plasticity : identification and characterization of targets and regulators.” 2014. Web. 19 Jan 2021.

Vancouver:

Pellentz-Lemattre C. Etude de la plasticité du protéasome : identification et caractérisation de cibles et de régulateurs : Study of proteasome plasticity : identification and characterization of targets and regulators. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2021 Jan 19]. Available from: http://www.theses.fr/2014PA112128.

Council of Science Editors:

Pellentz-Lemattre C. Etude de la plasticité du protéasome : identification et caractérisation de cibles et de régulateurs : Study of proteasome plasticity : identification and characterization of targets and regulators. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA112128


Leiden University

19. Annunziato, S. Precision modeling of breast cancer in the CRISPR era.

Degree: 2020, Leiden University

 The molecular mechanisms that instigate a healthy cell to become malignant are fueled by (epi)genetic alterations in so-called driver genes. While the Holy Grail of… (more)

Subjects/Keywords: breast cancer; mouse models; CRISPR-Cas9; gene editing; somatic models; intraductal injection; oncogenomics; genetic screens; drug resistance; PARP inhibitors; breast cancer; mouse models; CRISPR-Cas9; gene editing; somatic models; intraductal injection; oncogenomics; genetic screens; drug resistance; PARP inhibitors

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

APA (6th Edition):

Annunziato, S. (2020). Precision modeling of breast cancer in the CRISPR era. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/82703

Chicago Manual of Style (16th Edition):

Annunziato, S. “Precision modeling of breast cancer in the CRISPR era.” 2020. Doctoral Dissertation, Leiden University. Accessed January 19, 2021. http://hdl.handle.net/1887/82703.

MLA Handbook (7th Edition):

Annunziato, S. “Precision modeling of breast cancer in the CRISPR era.” 2020. Web. 19 Jan 2021.

Vancouver:

Annunziato S. Precision modeling of breast cancer in the CRISPR era. [Internet] [Doctoral dissertation]. Leiden University; 2020. [cited 2021 Jan 19]. Available from: http://hdl.handle.net/1887/82703.

Council of Science Editors:

Annunziato S. Precision modeling of breast cancer in the CRISPR era. [Doctoral Dissertation]. Leiden University; 2020. Available from: http://hdl.handle.net/1887/82703

.