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You searched for subject:(Small Interfering RNA). Showing records 1 – 30 of 182 total matches.

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Oregon State University

1. Montgomery, Taiowa A. Small RNA pathways in plants.

Degree: PhD, Molecular and Cellular Biology, 2008, Oregon State University

 miRNA-guided cleavage initiates entry of primary transcripts into the trans-acting siRNA (tasiRNA) biogenesis pathway involving RNA-DEPENDENT RNA POLYMERASE6 (RDR6), DICER-LIKE 4 (DCL4), and SUPPRESSOR OF… (more)

Subjects/Keywords: microRNA; Small interfering RNA

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APA (6th Edition):

Montgomery, T. A. (2008). Small RNA pathways in plants. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/9322

Chicago Manual of Style (16th Edition):

Montgomery, Taiowa A. “Small RNA pathways in plants.” 2008. Doctoral Dissertation, Oregon State University. Accessed December 01, 2020. http://hdl.handle.net/1957/9322.

MLA Handbook (7th Edition):

Montgomery, Taiowa A. “Small RNA pathways in plants.” 2008. Web. 01 Dec 2020.

Vancouver:

Montgomery TA. Small RNA pathways in plants. [Internet] [Doctoral dissertation]. Oregon State University; 2008. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1957/9322.

Council of Science Editors:

Montgomery TA. Small RNA pathways in plants. [Doctoral Dissertation]. Oregon State University; 2008. Available from: http://hdl.handle.net/1957/9322

2. Pandya, Isha. Small RNA Sequencing Analysis of Inner Ear from Conditional Knockout Mice with Hair Cell-Specific Dgcr8 or Dicer1 Deletion.

Degree: PhD, Biomedical Sciences (graduate program), 2016, Creighton University

 Damage to mechanosensory hair cells (HCs) of the inner ear leads to permanent hearing loss. Small RNAs, namely endogenous small interfering RNAs (endo-siRNAs) and canonical… (more)

Subjects/Keywords: RNA, Small Interfering; Hearing Loss

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APA (6th Edition):

Pandya, I. (2016). Small RNA Sequencing Analysis of Inner Ear from Conditional Knockout Mice with Hair Cell-Specific Dgcr8 or Dicer1 Deletion. (Doctoral Dissertation). Creighton University. Retrieved from http://hdl.handle.net/10504/74482

Chicago Manual of Style (16th Edition):

Pandya, Isha. “Small RNA Sequencing Analysis of Inner Ear from Conditional Knockout Mice with Hair Cell-Specific Dgcr8 or Dicer1 Deletion.” 2016. Doctoral Dissertation, Creighton University. Accessed December 01, 2020. http://hdl.handle.net/10504/74482.

MLA Handbook (7th Edition):

Pandya, Isha. “Small RNA Sequencing Analysis of Inner Ear from Conditional Knockout Mice with Hair Cell-Specific Dgcr8 or Dicer1 Deletion.” 2016. Web. 01 Dec 2020.

Vancouver:

Pandya I. Small RNA Sequencing Analysis of Inner Ear from Conditional Knockout Mice with Hair Cell-Specific Dgcr8 or Dicer1 Deletion. [Internet] [Doctoral dissertation]. Creighton University; 2016. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10504/74482.

Council of Science Editors:

Pandya I. Small RNA Sequencing Analysis of Inner Ear from Conditional Knockout Mice with Hair Cell-Specific Dgcr8 or Dicer1 Deletion. [Doctoral Dissertation]. Creighton University; 2016. Available from: http://hdl.handle.net/10504/74482


University of Utah

3. Welker, Noah Christopher. The Role of Caenorhabditis Elegans Dicer in Endogenous Small RNA Silencing Pathways.

Degree: PhD, Biochemistry;, 2010, University of Utah

RNA interference (RNAi) was originally identified as a conserved biological response to exogenous double-stranded RNA (dsRNA). During this response, dsRNA is processed into 21-23 nucleotide… (more)

Subjects/Keywords: Small Interfering RNA; Caenorhabditis elegans

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APA (6th Edition):

Welker, N. C. (2010). The Role of Caenorhabditis Elegans Dicer in Endogenous Small RNA Silencing Pathways. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/715/rec/1217

Chicago Manual of Style (16th Edition):

Welker, Noah Christopher. “The Role of Caenorhabditis Elegans Dicer in Endogenous Small RNA Silencing Pathways.” 2010. Doctoral Dissertation, University of Utah. Accessed December 01, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/715/rec/1217.

MLA Handbook (7th Edition):

Welker, Noah Christopher. “The Role of Caenorhabditis Elegans Dicer in Endogenous Small RNA Silencing Pathways.” 2010. Web. 01 Dec 2020.

Vancouver:

Welker NC. The Role of Caenorhabditis Elegans Dicer in Endogenous Small RNA Silencing Pathways. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2020 Dec 01]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/715/rec/1217.

Council of Science Editors:

Welker NC. The Role of Caenorhabditis Elegans Dicer in Endogenous Small RNA Silencing Pathways. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/715/rec/1217


University of Texas Southwestern Medical Center

4. Hoshiyama, Hirotoshi. Human shRNA Library Screening to Dissect Pathways Involved in Telomerase Actions.

Degree: 2011, University of Texas Southwestern Medical Center

 The minimal components of human telomerase are the human telomerase reverse transcriptase (hTERT) and the human telomerase template RNA (hTR). Although it is known that… (more)

Subjects/Keywords: RNA, Small Interfering; Telomeres; Sequence Analysis, RNA

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APA (6th Edition):

Hoshiyama, H. (2011). Human shRNA Library Screening to Dissect Pathways Involved in Telomerase Actions. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/944

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):

Hoshiyama, Hirotoshi. “Human shRNA Library Screening to Dissect Pathways Involved in Telomerase Actions.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed December 01, 2020. http://hdl.handle.net/2152.5/944.

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

MLA Handbook (7th Edition):

Hoshiyama, Hirotoshi. “Human shRNA Library Screening to Dissect Pathways Involved in Telomerase Actions.” 2011. Web. 01 Dec 2020.

Vancouver:

Hoshiyama H. Human shRNA Library Screening to Dissect Pathways Involved in Telomerase Actions. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152.5/944.

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

Council of Science Editors:

Hoshiyama H. Human shRNA Library Screening to Dissect Pathways Involved in Telomerase Actions. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/944

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


Rutgers University

5. Naqvi, Ammar S., 1984-. Temporal patterns of short non-coding RNA modifications and expression.

Degree: PhD, Computational and Integrative Biology, 2015, Rutgers University

We investigated the function and properties of small RNAs, particularly microRNAs and tRNA-derived fragments (tRFs) with age. We report the characterization of a novel 3'-to-… (more)

Subjects/Keywords: Non-coding RNA; Small interfering RNA

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APA (6th Edition):

Naqvi, Ammar S., 1. (2015). Temporal patterns of short non-coding RNA modifications and expression. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/47155/

Chicago Manual of Style (16th Edition):

Naqvi, Ammar S., 1984-. “Temporal patterns of short non-coding RNA modifications and expression.” 2015. Doctoral Dissertation, Rutgers University. Accessed December 01, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/47155/.

MLA Handbook (7th Edition):

Naqvi, Ammar S., 1984-. “Temporal patterns of short non-coding RNA modifications and expression.” 2015. Web. 01 Dec 2020.

Vancouver:

Naqvi, Ammar S. 1. Temporal patterns of short non-coding RNA modifications and expression. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2020 Dec 01]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47155/.

Council of Science Editors:

Naqvi, Ammar S. 1. Temporal patterns of short non-coding RNA modifications and expression. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47155/


Drexel University

6. Biba, Mirlinda. Chromatographic Analysis and Separation of Short RNA Oligonucleotides with Novel Liquid Chromatography Methods.

Degree: 2014, Drexel University

Synthetic oligonucleotides have become increasingly important as part of new developments in the use of antisense and small interfering ribonucleic acid (siRNA) as potential therapies… (more)

Subjects/Keywords: Chemistry; Oligonucleotides – Therapeutic use; Small interfering RNA

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APA (6th Edition):

Biba, M. (2014). Chromatographic Analysis and Separation of Short RNA Oligonucleotides with Novel Liquid Chromatography Methods. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/4530

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):

Biba, Mirlinda. “Chromatographic Analysis and Separation of Short RNA Oligonucleotides with Novel Liquid Chromatography Methods.” 2014. Thesis, Drexel University. Accessed December 01, 2020. http://hdl.handle.net/1860/4530.

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

MLA Handbook (7th Edition):

Biba, Mirlinda. “Chromatographic Analysis and Separation of Short RNA Oligonucleotides with Novel Liquid Chromatography Methods.” 2014. Web. 01 Dec 2020.

Vancouver:

Biba M. Chromatographic Analysis and Separation of Short RNA Oligonucleotides with Novel Liquid Chromatography Methods. [Internet] [Thesis]. Drexel University; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1860/4530.

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

Council of Science Editors:

Biba M. Chromatographic Analysis and Separation of Short RNA Oligonucleotides with Novel Liquid Chromatography Methods. [Thesis]. Drexel University; 2014. Available from: http://hdl.handle.net/1860/4530

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


University of Texas Southwestern Medical Center

7. Yu, Dongbo 1984-. Using Chemically Modified Oligonucleotides to Modulate Gene Expression, Treat Genetic Diseases, and Probe Novel Mechanisms of RNA Interference.

Degree: 2013, University of Texas Southwestern Medical Center

 A number of inherited neurological disorders remain incurable despite having well-defined monogenic etiologies. One example is Huntington's disease (HD), which is caused by CAG trinucleotide… (more)

Subjects/Keywords: Huntington Disease; Nerve Tissue Proteins; RNA Interference; RNA, Small Interfering

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APA (6th Edition):

Yu, D. 1. (2013). Using Chemically Modified Oligonucleotides to Modulate Gene Expression, Treat Genetic Diseases, and Probe Novel Mechanisms of RNA Interference. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/ETD-UTSWMED-2014-05-59

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):

Yu, Dongbo 1984-. “Using Chemically Modified Oligonucleotides to Modulate Gene Expression, Treat Genetic Diseases, and Probe Novel Mechanisms of RNA Interference.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed December 01, 2020. http://hdl.handle.net/2152.5/ETD-UTSWMED-2014-05-59.

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

MLA Handbook (7th Edition):

Yu, Dongbo 1984-. “Using Chemically Modified Oligonucleotides to Modulate Gene Expression, Treat Genetic Diseases, and Probe Novel Mechanisms of RNA Interference.” 2013. Web. 01 Dec 2020.

Vancouver:

Yu D1. Using Chemically Modified Oligonucleotides to Modulate Gene Expression, Treat Genetic Diseases, and Probe Novel Mechanisms of RNA Interference. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2014-05-59.

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

Council of Science Editors:

Yu D1. Using Chemically Modified Oligonucleotides to Modulate Gene Expression, Treat Genetic Diseases, and Probe Novel Mechanisms of RNA Interference. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/ETD-UTSWMED-2014-05-59

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


University of Delaware

8. Wang, Yue. Development of RNA-based molecules for the inhibition of influenza A virus.

Degree: PhD, University of Delaware, Department of Animal and Food Sciences, 2014, University of Delaware

 Avian influenza has always been a serious threat to the poultry industry and public health. Limitations in the effectiveness and possible adverse effects of vaccines… (more)

Subjects/Keywords: RNA.; Small interfering RNA.; Influenza A virus.; Virus inhibitors.

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APA (6th Edition):

Wang, Y. (2014). Development of RNA-based molecules for the inhibition of influenza A virus. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/13426

Chicago Manual of Style (16th Edition):

Wang, Yue. “Development of RNA-based molecules for the inhibition of influenza A virus.” 2014. Doctoral Dissertation, University of Delaware. Accessed December 01, 2020. http://udspace.udel.edu/handle/19716/13426.

MLA Handbook (7th Edition):

Wang, Yue. “Development of RNA-based molecules for the inhibition of influenza A virus.” 2014. Web. 01 Dec 2020.

Vancouver:

Wang Y. Development of RNA-based molecules for the inhibition of influenza A virus. [Internet] [Doctoral dissertation]. University of Delaware; 2014. [cited 2020 Dec 01]. Available from: http://udspace.udel.edu/handle/19716/13426.

Council of Science Editors:

Wang Y. Development of RNA-based molecules for the inhibition of influenza A virus. [Doctoral Dissertation]. University of Delaware; 2014. Available from: http://udspace.udel.edu/handle/19716/13426


University of Hong Kong

9. Leung, Oi-ning. Identification and characterization of E3 ubiquitin ligase SIAH1 as a regulatory target of microRNA-135a in HeLa cells.

Degree: 2008, University of Hong Kong

Subjects/Keywords: Small interfering RNA.; Ubiquitin.

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APA (6th Edition):

Leung, O. (2008). Identification and characterization of E3 ubiquitin ligase SIAH1 as a regulatory target of microRNA-135a in HeLa cells. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/51995

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):

Leung, Oi-ning. “Identification and characterization of E3 ubiquitin ligase SIAH1 as a regulatory target of microRNA-135a in HeLa cells.” 2008. Thesis, University of Hong Kong. Accessed December 01, 2020. http://hdl.handle.net/10722/51995.

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

MLA Handbook (7th Edition):

Leung, Oi-ning. “Identification and characterization of E3 ubiquitin ligase SIAH1 as a regulatory target of microRNA-135a in HeLa cells.” 2008. Web. 01 Dec 2020.

Vancouver:

Leung O. Identification and characterization of E3 ubiquitin ligase SIAH1 as a regulatory target of microRNA-135a in HeLa cells. [Internet] [Thesis]. University of Hong Kong; 2008. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10722/51995.

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

Council of Science Editors:

Leung O. Identification and characterization of E3 ubiquitin ligase SIAH1 as a regulatory target of microRNA-135a in HeLa cells. [Thesis]. University of Hong Kong; 2008. Available from: http://hdl.handle.net/10722/51995

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


Stellenbosch University

10. Dias, Stephanie. MicroRNA expression profiling in peripheral blood mononuclear cells and serum of type 2 diabetic, pre-diabetic and normo-glycaemic individuals.

Degree: MSc, Biomedical Sciences, 2016, Stellenbosch University

 ENGLISH ABSTRACT: MicroRNAs (miRNAs) are small non-coding RNAs that play a fundamental role in cellular function by regulating messenger RNA gene expression. Alterations in miRNA… (more)

Subjects/Keywords: UCTD; Small interfering RNA; Non-insulin-dependent diabetes

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APA (6th Edition):

Dias, S. (2016). MicroRNA expression profiling in peripheral blood mononuclear cells and serum of type 2 diabetic, pre-diabetic and normo-glycaemic individuals. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/98823

Chicago Manual of Style (16th Edition):

Dias, Stephanie. “MicroRNA expression profiling in peripheral blood mononuclear cells and serum of type 2 diabetic, pre-diabetic and normo-glycaemic individuals.” 2016. Masters Thesis, Stellenbosch University. Accessed December 01, 2020. http://hdl.handle.net/10019.1/98823.

MLA Handbook (7th Edition):

Dias, Stephanie. “MicroRNA expression profiling in peripheral blood mononuclear cells and serum of type 2 diabetic, pre-diabetic and normo-glycaemic individuals.” 2016. Web. 01 Dec 2020.

Vancouver:

Dias S. MicroRNA expression profiling in peripheral blood mononuclear cells and serum of type 2 diabetic, pre-diabetic and normo-glycaemic individuals. [Internet] [Masters thesis]. Stellenbosch University; 2016. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10019.1/98823.

Council of Science Editors:

Dias S. MicroRNA expression profiling in peripheral blood mononuclear cells and serum of type 2 diabetic, pre-diabetic and normo-glycaemic individuals. [Masters Thesis]. Stellenbosch University; 2016. Available from: http://hdl.handle.net/10019.1/98823


University of Newcastle

11. Mihalas, Bettina P. Molecular mechanisms contributing to the age-related decline in oocyte quality.

Degree: PhD, 2019, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

Maternal ageing is accompanied by a precipitous decline in oocyte quality, culminating in increased rates of congenital disabilities,… (more)

Subjects/Keywords: oocyte; oxidative stress; lipid peroxidation; small interfering RNA; thesis by publication

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APA (6th Edition):

Mihalas, B. P. (2019). Molecular mechanisms contributing to the age-related decline in oocyte quality. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1403623

Chicago Manual of Style (16th Edition):

Mihalas, Bettina P. “Molecular mechanisms contributing to the age-related decline in oocyte quality.” 2019. Doctoral Dissertation, University of Newcastle. Accessed December 01, 2020. http://hdl.handle.net/1959.13/1403623.

MLA Handbook (7th Edition):

Mihalas, Bettina P. “Molecular mechanisms contributing to the age-related decline in oocyte quality.” 2019. Web. 01 Dec 2020.

Vancouver:

Mihalas BP. Molecular mechanisms contributing to the age-related decline in oocyte quality. [Internet] [Doctoral dissertation]. University of Newcastle; 2019. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/1959.13/1403623.

Council of Science Editors:

Mihalas BP. Molecular mechanisms contributing to the age-related decline in oocyte quality. [Doctoral Dissertation]. University of Newcastle; 2019. Available from: http://hdl.handle.net/1959.13/1403623


University of Hong Kong

12. Liu, Ming-lai. Roles of microRNAs in hepatocellular carcinoma: biomarkers, matabolisms and pathway regulators.

Degree: 2011, University of Hong Kong

Subjects/Keywords: Small interfering RNA.; Liver - Cancer.

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APA (6th Edition):

Liu, M. (2011). Roles of microRNAs in hepatocellular carcinoma: biomarkers, matabolisms and pathway regulators. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/173968

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):

Liu, Ming-lai. “Roles of microRNAs in hepatocellular carcinoma: biomarkers, matabolisms and pathway regulators.” 2011. Thesis, University of Hong Kong. Accessed December 01, 2020. http://hdl.handle.net/10722/173968.

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

MLA Handbook (7th Edition):

Liu, Ming-lai. “Roles of microRNAs in hepatocellular carcinoma: biomarkers, matabolisms and pathway regulators.” 2011. Web. 01 Dec 2020.

Vancouver:

Liu M. Roles of microRNAs in hepatocellular carcinoma: biomarkers, matabolisms and pathway regulators. [Internet] [Thesis]. University of Hong Kong; 2011. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10722/173968.

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

Council of Science Editors:

Liu M. Roles of microRNAs in hepatocellular carcinoma: biomarkers, matabolisms and pathway regulators. [Thesis]. University of Hong Kong; 2011. Available from: http://hdl.handle.net/10722/173968

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


University of Hong Kong

13. 何廷軒. Immunostimulatory function of the defective interfering RNA of Sendai virus.

Degree: 2013, University of Hong Kong

 The Cantell strain of Sendai virus (SeV-C) represents a typical laboratory attenuated virus which is less virulent and able to induce large amount of interferon… (more)

Subjects/Keywords: Small interfering RNA; Sendai virus

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APA (6th Edition):

何廷軒. (2013). Immunostimulatory function of the defective interfering RNA of Sendai virus. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/197496

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

Chicago Manual of Style (16th Edition):

何廷軒. “Immunostimulatory function of the defective interfering RNA of Sendai virus.” 2013. Thesis, University of Hong Kong. Accessed December 01, 2020. http://hdl.handle.net/10722/197496.

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

MLA Handbook (7th Edition):

何廷軒. “Immunostimulatory function of the defective interfering RNA of Sendai virus.” 2013. Web. 01 Dec 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

何廷軒. Immunostimulatory function of the defective interfering RNA of Sendai virus. [Internet] [Thesis]. University of Hong Kong; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10722/197496.

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

Council of Science Editors:

何廷軒. Immunostimulatory function of the defective interfering RNA of Sendai virus. [Thesis]. University of Hong Kong; 2013. Available from: http://hdl.handle.net/10722/197496

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


Brock University

14. Zhao, Yuyan. Chemical synthesis of glycosylated oligoribonucleotides for siRNA development .

Degree: Department of Chemistry, 2009, Brock University

 In this study, an efficient methodology for the preparation of carbohydrate-RNA conjugates was established, which involved the use of 3,4~diethoxy-3-cyclobutene-l,2- dione (diethyl squarate) as the… (more)

Subjects/Keywords: Small interfering RNA – Synthesis.

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APA (6th Edition):

Zhao, Y. (2009). Chemical synthesis of glycosylated oligoribonucleotides for siRNA development . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/2849

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):

Zhao, Yuyan. “Chemical synthesis of glycosylated oligoribonucleotides for siRNA development .” 2009. Thesis, Brock University. Accessed December 01, 2020. http://hdl.handle.net/10464/2849.

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

MLA Handbook (7th Edition):

Zhao, Yuyan. “Chemical synthesis of glycosylated oligoribonucleotides for siRNA development .” 2009. Web. 01 Dec 2020.

Vancouver:

Zhao Y. Chemical synthesis of glycosylated oligoribonucleotides for siRNA development . [Internet] [Thesis]. Brock University; 2009. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10464/2849.

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

Council of Science Editors:

Zhao Y. Chemical synthesis of glycosylated oligoribonucleotides for siRNA development . [Thesis]. Brock University; 2009. Available from: http://hdl.handle.net/10464/2849

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


Montana State University

15. Schwartz, Elizabeth Ann. Behavioral consequences of calcium/calmodulin kinase II inhibition in rats.

Degree: MS, College of Letters & Science, 2005, Montana State University

 CaM kinase II (CaMKII) comprises 2% of hippocampal protein and plays an important role in learning and models of neural plasticity. Previous studies have employed… (more)

Subjects/Keywords: Behavior.; Small interfering RNA.

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APA (6th Edition):

Schwartz, E. A. (2005). Behavioral consequences of calcium/calmodulin kinase II inhibition in rats. (Masters Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/2222

Chicago Manual of Style (16th Edition):

Schwartz, Elizabeth Ann. “Behavioral consequences of calcium/calmodulin kinase II inhibition in rats.” 2005. Masters Thesis, Montana State University. Accessed December 01, 2020. https://scholarworks.montana.edu/xmlui/handle/1/2222.

MLA Handbook (7th Edition):

Schwartz, Elizabeth Ann. “Behavioral consequences of calcium/calmodulin kinase II inhibition in rats.” 2005. Web. 01 Dec 2020.

Vancouver:

Schwartz EA. Behavioral consequences of calcium/calmodulin kinase II inhibition in rats. [Internet] [Masters thesis]. Montana State University; 2005. [cited 2020 Dec 01]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2222.

Council of Science Editors:

Schwartz EA. Behavioral consequences of calcium/calmodulin kinase II inhibition in rats. [Masters Thesis]. Montana State University; 2005. Available from: https://scholarworks.montana.edu/xmlui/handle/1/2222


University of Georgia

16. Zhang, Wenliang. Disease intervention strategies against respiratory syncytial virus infection.

Degree: 2014, University of Georgia

 Respiratory syncytial virus (RSV) is a major cause of morbidity and some mortality in infants, young children, and the elderly worldwide. Currently, there is no… (more)

Subjects/Keywords: Respiratory syncytial virus; Small interfering RNA; Vaccine; Chemokine; Disease intevention

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APA (6th Edition):

Zhang, W. (2014). Disease intervention strategies against respiratory syncytial virus infection. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/25724

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):

Zhang, Wenliang. “Disease intervention strategies against respiratory syncytial virus infection.” 2014. Thesis, University of Georgia. Accessed December 01, 2020. http://hdl.handle.net/10724/25724.

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

MLA Handbook (7th Edition):

Zhang, Wenliang. “Disease intervention strategies against respiratory syncytial virus infection.” 2014. Web. 01 Dec 2020.

Vancouver:

Zhang W. Disease intervention strategies against respiratory syncytial virus infection. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10724/25724.

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

Council of Science Editors:

Zhang W. Disease intervention strategies against respiratory syncytial virus infection. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/25724

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


University of Texas – Austin

17. Liechty, William Blaine. Tunable, responsive nanoscale hydrogels for intracellular delivery of small interfering RNA.

Degree: PhD, Chemical Engineering, 2013, University of Texas – Austin

 Responsive, polybasic nanoscale hydrogels were synthesized using photoemulsion polymerization. The nanoscale hydrogels (nanogels) are approximately 50 nm in diameter and consist of a pH-responsive poly(2-(diethylaminoethyl… (more)

Subjects/Keywords: Hydrogel; Small interfering RNA; Responsive polymer; Drug delivery

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APA (6th Edition):

Liechty, W. B. (2013). Tunable, responsive nanoscale hydrogels for intracellular delivery of small interfering RNA. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/46258

Chicago Manual of Style (16th Edition):

Liechty, William Blaine. “Tunable, responsive nanoscale hydrogels for intracellular delivery of small interfering RNA.” 2013. Doctoral Dissertation, University of Texas – Austin. Accessed December 01, 2020. http://hdl.handle.net/2152/46258.

MLA Handbook (7th Edition):

Liechty, William Blaine. “Tunable, responsive nanoscale hydrogels for intracellular delivery of small interfering RNA.” 2013. Web. 01 Dec 2020.

Vancouver:

Liechty WB. Tunable, responsive nanoscale hydrogels for intracellular delivery of small interfering RNA. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2013. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152/46258.

Council of Science Editors:

Liechty WB. Tunable, responsive nanoscale hydrogels for intracellular delivery of small interfering RNA. [Doctoral Dissertation]. University of Texas – Austin; 2013. Available from: http://hdl.handle.net/2152/46258

18. Zhang, Zhao. piRNA Biogenesis and Transposon Silencing in Drosophila: A Dissertation.

Degree: Interdisciplinary Graduate Program, RNA Therapeutics Institute, 2013, U of Massachusetts : Med

  piRNAs guide PIWI proteins to silence transposons in animal germ cells. In Drosophila, the heterochromatic piRNA clusters transcribe piRNA precursors to be transported into… (more)

Subjects/Keywords: Small Interfering RNA; RNA Interference; DNA Transposable Elements; Drosophila Proteins; Molecular Genetics

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APA (6th Edition):

Zhang, Z. (2013). piRNA Biogenesis and Transposon Silencing in Drosophila: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/689

Chicago Manual of Style (16th Edition):

Zhang, Zhao. “piRNA Biogenesis and Transposon Silencing in Drosophila: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed December 01, 2020. http://escholarship.umassmed.edu/gsbs_diss/689.

MLA Handbook (7th Edition):

Zhang, Zhao. “piRNA Biogenesis and Transposon Silencing in Drosophila: A Dissertation.” 2013. Web. 01 Dec 2020.

Vancouver:

Zhang Z. piRNA Biogenesis and Transposon Silencing in Drosophila: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2020 Dec 01]. Available from: http://escholarship.umassmed.edu/gsbs_diss/689.

Council of Science Editors:

Zhang Z. piRNA Biogenesis and Transposon Silencing in Drosophila: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/689


University of Texas Southwestern Medical Center

19. Zhang, Zhenyu. The Mechanism of Small Interfering RNA Biogenesis in Neurospora Crassa.

Degree: 2014, University of Texas Southwestern Medical Center

RNA interference is a well-conserved post-transcriptional gene silencing mechanism that regulates various biological processes including development, genome defense, and heterochromatin formation. In filamentous fungus Neurospora… (more)

Subjects/Keywords: Homologous Recombination; Neurospora; Repetitive Sequences, Nucleic Acid; RNA Interference; RNA, Small Interfering

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APA (6th Edition):

Zhang, Z. (2014). The Mechanism of Small Interfering RNA Biogenesis in Neurospora Crassa. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3334

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):

Zhang, Zhenyu. “The Mechanism of Small Interfering RNA Biogenesis in Neurospora Crassa.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed December 01, 2020. http://hdl.handle.net/2152.5/3334.

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

MLA Handbook (7th Edition):

Zhang, Zhenyu. “The Mechanism of Small Interfering RNA Biogenesis in Neurospora Crassa.” 2014. Web. 01 Dec 2020.

Vancouver:

Zhang Z. The Mechanism of Small Interfering RNA Biogenesis in Neurospora Crassa. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152.5/3334.

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

Council of Science Editors:

Zhang Z. The Mechanism of Small Interfering RNA Biogenesis in Neurospora Crassa. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3334

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


University of Johannesburg

20. Lugongolo, Masixole Yvonne. Using sodium bisulphite treatment and PCR to construct mammalian anti-HIV-1 long hairpin RNA expression cassettes.

Degree: 2012, University of Johannesburg

M.Tech.

RNA interference (RNAi) is a gene silencing mechanism that uses short RNA duplexes to block gene expression. This mechanism has been widely explored to… (more)

Subjects/Keywords: RNA editing; HIV (Viruses); Polymerase chain reaction; Sodium sulfate; Small interfering RNA

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APA (6th Edition):

Lugongolo, M. Y. (2012). Using sodium bisulphite treatment and PCR to construct mammalian anti-HIV-1 long hairpin RNA expression cassettes. (Thesis). University of Johannesburg. Retrieved from http://hdl.handle.net/10210/4686

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):

Lugongolo, Masixole Yvonne. “Using sodium bisulphite treatment and PCR to construct mammalian anti-HIV-1 long hairpin RNA expression cassettes.” 2012. Thesis, University of Johannesburg. Accessed December 01, 2020. http://hdl.handle.net/10210/4686.

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

MLA Handbook (7th Edition):

Lugongolo, Masixole Yvonne. “Using sodium bisulphite treatment and PCR to construct mammalian anti-HIV-1 long hairpin RNA expression cassettes.” 2012. Web. 01 Dec 2020.

Vancouver:

Lugongolo MY. Using sodium bisulphite treatment and PCR to construct mammalian anti-HIV-1 long hairpin RNA expression cassettes. [Internet] [Thesis]. University of Johannesburg; 2012. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10210/4686.

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

Council of Science Editors:

Lugongolo MY. Using sodium bisulphite treatment and PCR to construct mammalian anti-HIV-1 long hairpin RNA expression cassettes. [Thesis]. University of Johannesburg; 2012. Available from: http://hdl.handle.net/10210/4686

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


Michigan State University

21. Kini, Hemant Kamalakar. Interaction of dicer, TRBP with short interfering RNAs : effect on silencing efficacy of siRNAs.

Degree: PhD, Department of Chemical Engineering, 2009, Michigan State University

Subjects/Keywords: Small interfering RNA; Gene silencing; RNA

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APA (6th Edition):

Kini, H. K. (2009). Interaction of dicer, TRBP with short interfering RNAs : effect on silencing efficacy of siRNAs. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:17163

Chicago Manual of Style (16th Edition):

Kini, Hemant Kamalakar. “Interaction of dicer, TRBP with short interfering RNAs : effect on silencing efficacy of siRNAs.” 2009. Doctoral Dissertation, Michigan State University. Accessed December 01, 2020. http://etd.lib.msu.edu/islandora/object/etd:17163.

MLA Handbook (7th Edition):

Kini, Hemant Kamalakar. “Interaction of dicer, TRBP with short interfering RNAs : effect on silencing efficacy of siRNAs.” 2009. Web. 01 Dec 2020.

Vancouver:

Kini HK. Interaction of dicer, TRBP with short interfering RNAs : effect on silencing efficacy of siRNAs. [Internet] [Doctoral dissertation]. Michigan State University; 2009. [cited 2020 Dec 01]. Available from: http://etd.lib.msu.edu/islandora/object/etd:17163.

Council of Science Editors:

Kini HK. Interaction of dicer, TRBP with short interfering RNAs : effect on silencing efficacy of siRNAs. [Doctoral Dissertation]. Michigan State University; 2009. Available from: http://etd.lib.msu.edu/islandora/object/etd:17163


University of Western Ontario

22. Way, Colin J. Folate Receptor-Targeting Liposomes for the Delivery of Antisense Molecules to Cancer Cells.

Degree: 2013, University of Western Ontario

 RNAi (RNA interference) is emerging as a promising tool for cancer therapy. Small interfering RNA (siRNA) molecules are activated in that pathway to reduce specific… (more)

Subjects/Keywords: Cationic liposomes; folate receptor; cancer; small interfering RNA (siRNA); RNA interference; thymidylate synthase; Macromolecular Substances

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APA (6th Edition):

Way, C. J. (2013). Folate Receptor-Targeting Liposomes for the Delivery of Antisense Molecules to Cancer Cells. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/1485

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):

Way, Colin J. “Folate Receptor-Targeting Liposomes for the Delivery of Antisense Molecules to Cancer Cells.” 2013. Thesis, University of Western Ontario. Accessed December 01, 2020. https://ir.lib.uwo.ca/etd/1485.

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

MLA Handbook (7th Edition):

Way, Colin J. “Folate Receptor-Targeting Liposomes for the Delivery of Antisense Molecules to Cancer Cells.” 2013. Web. 01 Dec 2020.

Vancouver:

Way CJ. Folate Receptor-Targeting Liposomes for the Delivery of Antisense Molecules to Cancer Cells. [Internet] [Thesis]. University of Western Ontario; 2013. [cited 2020 Dec 01]. Available from: https://ir.lib.uwo.ca/etd/1485.

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

Council of Science Editors:

Way CJ. Folate Receptor-Targeting Liposomes for the Delivery of Antisense Molecules to Cancer Cells. [Thesis]. University of Western Ontario; 2013. Available from: https://ir.lib.uwo.ca/etd/1485

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


University of Texas Southwestern Medical Center

23. Carstens, Ryan Murray. Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer.

Degree: 2015, University of Texas Southwestern Medical Center

 Nuclear hormone receptors are master regulators of diverse cellular functions implicated in tumor pathogenesis and as oncogenic drivers of many human cancers. To better understand… (more)

Subjects/Keywords: Carcinoma, Non-Small-Cell Lung; Receptors, Cytoplasmic and Nuclear; RNA, Small Interfering

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APA (6th Edition):

Carstens, R. M. (2015). Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4115

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):

Carstens, Ryan Murray. “Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed December 01, 2020. http://hdl.handle.net/2152.5/4115.

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

MLA Handbook (7th Edition):

Carstens, Ryan Murray. “Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer.” 2015. Web. 01 Dec 2020.

Vancouver:

Carstens RM. Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/2152.5/4115.

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

Council of Science Editors:

Carstens RM. Exploration of Nuclear Receptor Activity and siRNA-Derived Phenotypes as Therapeutics in Non-Small Cell Lung Cancer. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4115

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


Universitat Politècnica de València

24. Minoia, Sofia. Degradación in vivo de un viroide de replicación nuclear: rutas catalizadas por proteínas Argonauta cargadas con pequeños RNAs viroidales y por otras ribonucleasas que generan RNAs subgenómicos.

Degree: 2015, Universitat Politècnica de València

 Los viroides, los agentes infecciosos más simples de la escala biológica, están constituidos por una molécula circular de RNA monocatenario de aproximadamente 250-400 nucleótios (nt)… (more)

Subjects/Keywords: Viroids; Small-non-coding RNAs; Small interfering RNAs; RNA silencing; Argonaute proteins; Viroid subgenomic RNAs

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APA (6th Edition):

Minoia, S. (2015). Degradación in vivo de un viroide de replicación nuclear: rutas catalizadas por proteínas Argonauta cargadas con pequeños RNAs viroidales y por otras ribonucleasas que generan RNAs subgenómicos. (Doctoral Dissertation). Universitat Politècnica de València. Retrieved from http://hdl.handle.net/10251/48553

Chicago Manual of Style (16th Edition):

Minoia, Sofia. “Degradación in vivo de un viroide de replicación nuclear: rutas catalizadas por proteínas Argonauta cargadas con pequeños RNAs viroidales y por otras ribonucleasas que generan RNAs subgenómicos. ” 2015. Doctoral Dissertation, Universitat Politècnica de València. Accessed December 01, 2020. http://hdl.handle.net/10251/48553.

MLA Handbook (7th Edition):

Minoia, Sofia. “Degradación in vivo de un viroide de replicación nuclear: rutas catalizadas por proteínas Argonauta cargadas con pequeños RNAs viroidales y por otras ribonucleasas que generan RNAs subgenómicos. ” 2015. Web. 01 Dec 2020.

Vancouver:

Minoia S. Degradación in vivo de un viroide de replicación nuclear: rutas catalizadas por proteínas Argonauta cargadas con pequeños RNAs viroidales y por otras ribonucleasas que generan RNAs subgenómicos. [Internet] [Doctoral dissertation]. Universitat Politècnica de València; 2015. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10251/48553.

Council of Science Editors:

Minoia S. Degradación in vivo de un viroide de replicación nuclear: rutas catalizadas por proteínas Argonauta cargadas con pequeños RNAs viroidales y por otras ribonucleasas que generan RNAs subgenómicos. [Doctoral Dissertation]. Universitat Politècnica de València; 2015. Available from: http://hdl.handle.net/10251/48553


University of Florida

25. Yao, Bing. GW182 Silences microRNA Targets by Divergent Functional Domains and Regulates microRNA Stability.

Degree: PhD, Medical Sciences - Molecular Cell Biology (IDP), 2012, University of Florida

 MicroRNA (miRNA) is a relatively new class of shortendogenous non-coding RNA. MiRNA can pair to the 3’ untranslated region ofmRNA. This interaction inactivates protein translation… (more)

Subjects/Keywords: Exosomes; Journalism; Messenger RNA; MicroRNAs; Proteins; Repression; RNA; RNA stability; Small interfering RNA; Transfection; argonaute  – gw182  – microrna

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APA (6th Edition):

Yao, B. (2012). GW182 Silences microRNA Targets by Divergent Functional Domains and Regulates microRNA Stability. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0044363

Chicago Manual of Style (16th Edition):

Yao, Bing. “GW182 Silences microRNA Targets by Divergent Functional Domains and Regulates microRNA Stability.” 2012. Doctoral Dissertation, University of Florida. Accessed December 01, 2020. https://ufdc.ufl.edu/UFE0044363.

MLA Handbook (7th Edition):

Yao, Bing. “GW182 Silences microRNA Targets by Divergent Functional Domains and Regulates microRNA Stability.” 2012. Web. 01 Dec 2020.

Vancouver:

Yao B. GW182 Silences microRNA Targets by Divergent Functional Domains and Regulates microRNA Stability. [Internet] [Doctoral dissertation]. University of Florida; 2012. [cited 2020 Dec 01]. Available from: https://ufdc.ufl.edu/UFE0044363.

Council of Science Editors:

Yao B. GW182 Silences microRNA Targets by Divergent Functional Domains and Regulates microRNA Stability. [Doctoral Dissertation]. University of Florida; 2012. Available from: https://ufdc.ufl.edu/UFE0044363


University of Florida

26. SRIRAM,SRINIWAS. Knockdown of Connective Tissue Growth Factor(ctgf), Transforming Growth Factor Beta 1 (tgf-B1) and Transforming Growth Factor Beta Receptor 2 (tgf-Br2) by the Topical Application of Short Interfering Rna Molecules in Rabbit Corneal Fibroblasts.

Degree: MS, Biomedical Engineering, 2011, University of Florida

 Purpose: Transforming Growth Factor ? (TGF-?) is a key mediator of the fibrotic response to wounding. It is up regulated during different types of wound… (more)

Subjects/Keywords: Cell extracts; Cell growth; Fibroblasts; Messenger RNA; Rabbits; Reagents; RNA; Small interfering RNA; Transfection; Wound healing; CTGF  – RBCF  – SIRNA  – TGF  – TGFBR2

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APA (6th Edition):

SRIRAM,SRINIWAS. (2011). Knockdown of Connective Tissue Growth Factor(ctgf), Transforming Growth Factor Beta 1 (tgf-B1) and Transforming Growth Factor Beta Receptor 2 (tgf-Br2) by the Topical Application of Short Interfering Rna Molecules in Rabbit Corneal Fibroblasts. (Masters Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0043062

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

SRIRAM,SRINIWAS. “Knockdown of Connective Tissue Growth Factor(ctgf), Transforming Growth Factor Beta 1 (tgf-B1) and Transforming Growth Factor Beta Receptor 2 (tgf-Br2) by the Topical Application of Short Interfering Rna Molecules in Rabbit Corneal Fibroblasts.” 2011. Masters Thesis, University of Florida. Accessed December 01, 2020. https://ufdc.ufl.edu/UFE0043062.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

SRIRAM,SRINIWAS. “Knockdown of Connective Tissue Growth Factor(ctgf), Transforming Growth Factor Beta 1 (tgf-B1) and Transforming Growth Factor Beta Receptor 2 (tgf-Br2) by the Topical Application of Short Interfering Rna Molecules in Rabbit Corneal Fibroblasts.” 2011. Web. 01 Dec 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

SRIRAM,SRINIWAS. Knockdown of Connective Tissue Growth Factor(ctgf), Transforming Growth Factor Beta 1 (tgf-B1) and Transforming Growth Factor Beta Receptor 2 (tgf-Br2) by the Topical Application of Short Interfering Rna Molecules in Rabbit Corneal Fibroblasts. [Internet] [Masters thesis]. University of Florida; 2011. [cited 2020 Dec 01]. Available from: https://ufdc.ufl.edu/UFE0043062.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

SRIRAM,SRINIWAS. Knockdown of Connective Tissue Growth Factor(ctgf), Transforming Growth Factor Beta 1 (tgf-B1) and Transforming Growth Factor Beta Receptor 2 (tgf-Br2) by the Topical Application of Short Interfering Rna Molecules in Rabbit Corneal Fibroblasts. [Masters Thesis]. University of Florida; 2011. Available from: https://ufdc.ufl.edu/UFE0043062

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Florida

27. Sriram, Sriniwas. Synergistic Triple Combination of siRNAs to Knockdown Key Growth Factors and Receptors That Regulate Corneal Haze in Rabbits.

Degree: PhD, Biomedical Engineering, 2013, University of Florida

 Purpose The Transforming Growth Factor ß1 (TGFB1), TGFB receptor (TGFBR2) and Connective Tissue Growth Factor (CTGF) are key regulators of fibrosis in the cornea and… (more)

Subjects/Keywords: Cornea; Fibroblasts; Messenger RNA; Nanoparticles; Organ culture techniques; Rabbits; RNA; Scars; Small interfering RNA; Transfection; cornea  – scarring  – sirna  – synergy

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APA (6th Edition):

Sriram, S. (2013). Synergistic Triple Combination of siRNAs to Knockdown Key Growth Factors and Receptors That Regulate Corneal Haze in Rabbits. (Doctoral Dissertation). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0046091

Chicago Manual of Style (16th Edition):

Sriram, Sriniwas. “Synergistic Triple Combination of siRNAs to Knockdown Key Growth Factors and Receptors That Regulate Corneal Haze in Rabbits.” 2013. Doctoral Dissertation, University of Florida. Accessed December 01, 2020. https://ufdc.ufl.edu/UFE0046091.

MLA Handbook (7th Edition):

Sriram, Sriniwas. “Synergistic Triple Combination of siRNAs to Knockdown Key Growth Factors and Receptors That Regulate Corneal Haze in Rabbits.” 2013. Web. 01 Dec 2020.

Vancouver:

Sriram S. Synergistic Triple Combination of siRNAs to Knockdown Key Growth Factors and Receptors That Regulate Corneal Haze in Rabbits. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2020 Dec 01]. Available from: https://ufdc.ufl.edu/UFE0046091.

Council of Science Editors:

Sriram S. Synergistic Triple Combination of siRNAs to Knockdown Key Growth Factors and Receptors That Regulate Corneal Haze in Rabbits. [Doctoral Dissertation]. University of Florida; 2013. Available from: https://ufdc.ufl.edu/UFE0046091


University of Florida

28. Fitzpatrick, Daniel M. Escape from Short-Interfering RNA-Induced Silencing in an Orthobunyavirus, Tensaw Virus.

Degree: MS, Entomology and Nematology, 2013, University of Florida

 Ribonucleic acid interference (RNAi) is a major component of antiviral immunity in dipteran insects, including mosquitoes. Virus-specific short-interfering RNA (siRNA) are being considered as a… (more)

Subjects/Keywords: Antivirals; Cell growth; Hela cells; Infections; Nonsense; RNA; RNA interference; Small interfering RNA; Vero cells; Viruses; arbovirus  – entomology  – mosquito  – rnai  – virus

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APA (6th Edition):

Fitzpatrick, D. M. (2013). Escape from Short-Interfering RNA-Induced Silencing in an Orthobunyavirus, Tensaw Virus. (Masters Thesis). University of Florida. Retrieved from https://ufdc.ufl.edu/UFE0045564

Chicago Manual of Style (16th Edition):

Fitzpatrick, Daniel M. “Escape from Short-Interfering RNA-Induced Silencing in an Orthobunyavirus, Tensaw Virus.” 2013. Masters Thesis, University of Florida. Accessed December 01, 2020. https://ufdc.ufl.edu/UFE0045564.

MLA Handbook (7th Edition):

Fitzpatrick, Daniel M. “Escape from Short-Interfering RNA-Induced Silencing in an Orthobunyavirus, Tensaw Virus.” 2013. Web. 01 Dec 2020.

Vancouver:

Fitzpatrick DM. Escape from Short-Interfering RNA-Induced Silencing in an Orthobunyavirus, Tensaw Virus. [Internet] [Masters thesis]. University of Florida; 2013. [cited 2020 Dec 01]. Available from: https://ufdc.ufl.edu/UFE0045564.

Council of Science Editors:

Fitzpatrick DM. Escape from Short-Interfering RNA-Induced Silencing in an Orthobunyavirus, Tensaw Virus. [Masters Thesis]. University of Florida; 2013. Available from: https://ufdc.ufl.edu/UFE0045564


University of Missouri – Kansas City

29. Jain, Akshay. Development of Protein Based PCBP2 siRNA Nanocomplex for Liver Fibrosis Therapy.

Degree: PhD, 2018, University of Missouri – Kansas City

 The objective of this dissertation is to develop a protein-based siRNA nanocomplex for the treatment of alcoholic liver fibrosis. Our laboratory recently discovered that silencing… (more)

Subjects/Keywords: Liver  – Cirrhosis  – Treatment; Small interfering RNA; Liver Cirrhosis  – therapy; RNA, Small Interfering; Dissertation  – University of Missouri – Kansas City  – Pharmacy; Dissertation  – University of Missouri – Kansas City  – Chemistry

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

APA (6th Edition):

Jain, A. (2018). Development of Protein Based PCBP2 siRNA Nanocomplex for Liver Fibrosis Therapy. (Doctoral Dissertation). University of Missouri – Kansas City. Retrieved from http://hdl.handle.net/10355/70641

Chicago Manual of Style (16th Edition):

Jain, Akshay. “Development of Protein Based PCBP2 siRNA Nanocomplex for Liver Fibrosis Therapy.” 2018. Doctoral Dissertation, University of Missouri – Kansas City. Accessed December 01, 2020. http://hdl.handle.net/10355/70641.

MLA Handbook (7th Edition):

Jain, Akshay. “Development of Protein Based PCBP2 siRNA Nanocomplex for Liver Fibrosis Therapy.” 2018. Web. 01 Dec 2020.

Vancouver:

Jain A. Development of Protein Based PCBP2 siRNA Nanocomplex for Liver Fibrosis Therapy. [Internet] [Doctoral dissertation]. University of Missouri – Kansas City; 2018. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10355/70641.

Council of Science Editors:

Jain A. Development of Protein Based PCBP2 siRNA Nanocomplex for Liver Fibrosis Therapy. [Doctoral Dissertation]. University of Missouri – Kansas City; 2018. Available from: http://hdl.handle.net/10355/70641


University of Hong Kong

30. 余麗賢. MicroRNA-125 and FBI-1 in choriocarcinoma.

Degree: 2014, University of Hong Kong

 Choriocarcinoma is a malignant form of gestational trophoblastic disease arising from the trophoblastic epithelium. It is characterized by the presence of a mixed population of… (more)

Subjects/Keywords: Transcription factors; Choriocarcinoma; Small interfering RNA

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

APA (6th Edition):

余麗賢. (2014). MicroRNA-125 and FBI-1 in choriocarcinoma. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/206592

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

Chicago Manual of Style (16th Edition):

余麗賢. “MicroRNA-125 and FBI-1 in choriocarcinoma.” 2014. Thesis, University of Hong Kong. Accessed December 01, 2020. http://hdl.handle.net/10722/206592.

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

MLA Handbook (7th Edition):

余麗賢. “MicroRNA-125 and FBI-1 in choriocarcinoma.” 2014. Web. 01 Dec 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

余麗賢. MicroRNA-125 and FBI-1 in choriocarcinoma. [Internet] [Thesis]. University of Hong Kong; 2014. [cited 2020 Dec 01]. Available from: http://hdl.handle.net/10722/206592.

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

Council of Science Editors:

余麗賢. MicroRNA-125 and FBI-1 in choriocarcinoma. [Thesis]. University of Hong Kong; 2014. Available from: http://hdl.handle.net/10722/206592

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

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