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You searched for subject:(siRNA). Showing records 1 – 30 of 453 total matches.

[1] [2] [3] [4] [5] … [16]

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1. Mota, Jorge Alexandre Pereira. Development and optimization of a methodology to synthetize chitosan/cetuximab conjugates for encapsulate siRNA and targeting to EGFR overexpressing cells.

Degree: 2014, RCAAP

 O uso terapêutico de Small Interfering RNA (siRNA) tem sido observado como uma potencial nova abordagem para o tratamento do cancro. O desafio-chave no campo… (more)

Subjects/Keywords: SiRNA; EGFR

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

APA (6th Edition):

Mota, J. A. P. (2014). Development and optimization of a methodology to synthetize chitosan/cetuximab conjugates for encapsulate siRNA and targeting to EGFR overexpressing cells. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/368

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):

Mota, Jorge Alexandre Pereira. “Development and optimization of a methodology to synthetize chitosan/cetuximab conjugates for encapsulate siRNA and targeting to EGFR overexpressing cells.” 2014. Thesis, RCAAP. Accessed April 07, 2020. https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/368.

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

MLA Handbook (7th Edition):

Mota, Jorge Alexandre Pereira. “Development and optimization of a methodology to synthetize chitosan/cetuximab conjugates for encapsulate siRNA and targeting to EGFR overexpressing cells.” 2014. Web. 07 Apr 2020.

Vancouver:

Mota JAP. Development and optimization of a methodology to synthetize chitosan/cetuximab conjugates for encapsulate siRNA and targeting to EGFR overexpressing cells. [Internet] [Thesis]. RCAAP; 2014. [cited 2020 Apr 07]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/368.

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

Council of Science Editors:

Mota JAP. Development and optimization of a methodology to synthetize chitosan/cetuximab conjugates for encapsulate siRNA and targeting to EGFR overexpressing cells. [Thesis]. RCAAP; 2014. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.cespu.pt:20.500.11816/368

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


Texas A&M University

2. Chern, Christina. The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications.

Degree: 2009, Texas A&M University

 The study of drug delivery for the treatment of illnesses and injuries is an important area of pharmaceutical technology. A relatively new area of drug… (more)

Subjects/Keywords: gene therapy; siRNA

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APA (6th Edition):

Chern, C. (2009). The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2327

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):

Chern, Christina. “The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications.” 2009. Thesis, Texas A&M University. Accessed April 07, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2327.

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

MLA Handbook (7th Edition):

Chern, Christina. “The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications.” 2009. Web. 07 Apr 2020.

Vancouver:

Chern C. The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2327.

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

Council of Science Editors:

Chern C. The investigation of controlled release microchips, nanoparticles, and sirna for gene therapy in tissue engineering applications. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2327

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


University of Arizona

3. Monasky, Ross Calvin. The Role of EspH and Host Cell Proteins in Enteropathogenic Escherichia Coli-Induced Cell Death and Virulence .

Degree: 2018, University of Arizona

 Enteropathogenic Escherichia coli (EPEC) is a leading cause of infantile diarrhea, particularly in developing countries. EPEC belongs to the attaching and effacing (A/E) family of… (more)

Subjects/Keywords: Apoptosis; EPEC; siRNA

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APA (6th Edition):

Monasky, R. C. (2018). The Role of EspH and Host Cell Proteins in Enteropathogenic Escherichia Coli-Induced Cell Death and Virulence . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/628172

Chicago Manual of Style (16th Edition):

Monasky, Ross Calvin. “The Role of EspH and Host Cell Proteins in Enteropathogenic Escherichia Coli-Induced Cell Death and Virulence .” 2018. Masters Thesis, University of Arizona. Accessed April 07, 2020. http://hdl.handle.net/10150/628172.

MLA Handbook (7th Edition):

Monasky, Ross Calvin. “The Role of EspH and Host Cell Proteins in Enteropathogenic Escherichia Coli-Induced Cell Death and Virulence .” 2018. Web. 07 Apr 2020.

Vancouver:

Monasky RC. The Role of EspH and Host Cell Proteins in Enteropathogenic Escherichia Coli-Induced Cell Death and Virulence . [Internet] [Masters thesis]. University of Arizona; 2018. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/10150/628172.

Council of Science Editors:

Monasky RC. The Role of EspH and Host Cell Proteins in Enteropathogenic Escherichia Coli-Induced Cell Death and Virulence . [Masters Thesis]. University of Arizona; 2018. Available from: http://hdl.handle.net/10150/628172


University of Alberta

4. Falamarzian, Arash. Lipid modification of polymeric nanocarriers for drug and siRNA delivery.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2013, University of Alberta

 The use of nanotechnology in pharmaceutical development has progressed significantly in recent decades. This rapid advancement is driven by crucial need for improving the performance… (more)

Subjects/Keywords: siRNA; Amphotericin B; Nanocarrier; Micelle

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APA (6th Edition):

Falamarzian, A. (2013). Lipid modification of polymeric nanocarriers for drug and siRNA delivery. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/p8418n60j

Chicago Manual of Style (16th Edition):

Falamarzian, Arash. “Lipid modification of polymeric nanocarriers for drug and siRNA delivery.” 2013. Doctoral Dissertation, University of Alberta. Accessed April 07, 2020. https://era.library.ualberta.ca/files/p8418n60j.

MLA Handbook (7th Edition):

Falamarzian, Arash. “Lipid modification of polymeric nanocarriers for drug and siRNA delivery.” 2013. Web. 07 Apr 2020.

Vancouver:

Falamarzian A. Lipid modification of polymeric nanocarriers for drug and siRNA delivery. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2020 Apr 07]. Available from: https://era.library.ualberta.ca/files/p8418n60j.

Council of Science Editors:

Falamarzian A. Lipid modification of polymeric nanocarriers for drug and siRNA delivery. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/p8418n60j

5. 岡野, 陽介. 植物においてsiRNAが誘導するDNAとクロマチンの修飾 : siRNA targeting of endogenous promoters induces DNA methylation but not necessarily gene silencing in rice; ショクブツ ニオイテ siRNA ガ ユウドウスル DNA ト クロマチン ノ シュウショク.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: イネ; siRNA

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APA (6th Edition):

岡野, . (n.d.). 植物においてsiRNAが誘導するDNAとクロマチンの修飾 : siRNA targeting of endogenous promoters induces DNA methylation but not necessarily gene silencing in rice; ショクブツ ニオイテ siRNA ガ ユウドウスル DNA ト クロマチン ノ シュウショク. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/4114

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

Chicago Manual of Style (16th Edition):

岡野, 陽介. “植物においてsiRNAが誘導するDNAとクロマチンの修飾 : siRNA targeting of endogenous promoters induces DNA methylation but not necessarily gene silencing in rice; ショクブツ ニオイテ siRNA ガ ユウドウスル DNA ト クロマチン ノ シュウショク.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed April 07, 2020. http://hdl.handle.net/10061/4114.

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

MLA Handbook (7th Edition):

岡野, 陽介. “植物においてsiRNAが誘導するDNAとクロマチンの修飾 : siRNA targeting of endogenous promoters induces DNA methylation but not necessarily gene silencing in rice; ショクブツ ニオイテ siRNA ガ ユウドウスル DNA ト クロマチン ノ シュウショク.” Web. 07 Apr 2020.

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

Vancouver:

岡野 . 植物においてsiRNAが誘導するDNAとクロマチンの修飾 : siRNA targeting of endogenous promoters induces DNA methylation but not necessarily gene silencing in rice; ショクブツ ニオイテ siRNA ガ ユウドウスル DNA ト クロマチン ノ シュウショク. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2020 Apr 07]. Available from: http://hdl.handle.net/10061/4114.

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

Council of Science Editors:

岡野 . 植物においてsiRNAが誘導するDNAとクロマチンの修飾 : siRNA targeting of endogenous promoters induces DNA methylation but not necessarily gene silencing in rice; ショクブツ ニオイテ siRNA ガ ユウドウスル DNA ト クロマチン ノ シュウショク. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/4114

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


Penn State University

6. Sutermaster, Bryan A. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.

Degree: MS, Bioengineering, 2012, Penn State University

 Nanoliposomes continue to be an interesting candidate for overcoming disadvantages in conventional systemic drug delivery, including off-target toxicities and short circulation times. Various modifications, like… (more)

Subjects/Keywords: liposome; siRNA; cancer; drug delivery

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APA (6th Edition):

Sutermaster, B. A. (2012). Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/15235

Chicago Manual of Style (16th Edition):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Masters Thesis, Penn State University. Accessed April 07, 2020. https://etda.libraries.psu.edu/catalog/15235.

MLA Handbook (7th Edition):

Sutermaster, Bryan A. “Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors.” 2012. Web. 07 Apr 2020.

Vancouver:

Sutermaster BA. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. [Internet] [Masters thesis]. Penn State University; 2012. [cited 2020 Apr 07]. Available from: https://etda.libraries.psu.edu/catalog/15235.

Council of Science Editors:

Sutermaster BA. Development of Novel Ultra-Deformable Cationic Liposomes for siRNA Delivery to Fibrous Tumors. [Masters Thesis]. Penn State University; 2012. Available from: https://etda.libraries.psu.edu/catalog/15235


Penn State University

7. Tran, Melissa Ann. TREATMENT OF MELANOMA AND BREAST CANCER WITH GENETIC BASED LIPOSOMAL DRUG FORMULATIONS.

Degree: PhD, Genetics, 2008, Penn State University

 Treatment options for patients with cancers such as breast carcinoma and melanoma are poor with early detection as the best therapy. For patients with advanced… (more)

Subjects/Keywords: siRNA; liposomes; melanoma; ultrasound

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APA (6th Edition):

Tran, M. A. (2008). TREATMENT OF MELANOMA AND BREAST CANCER WITH GENETIC BASED LIPOSOMAL DRUG FORMULATIONS. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8430

Chicago Manual of Style (16th Edition):

Tran, Melissa Ann. “TREATMENT OF MELANOMA AND BREAST CANCER WITH GENETIC BASED LIPOSOMAL DRUG FORMULATIONS.” 2008. Doctoral Dissertation, Penn State University. Accessed April 07, 2020. https://etda.libraries.psu.edu/catalog/8430.

MLA Handbook (7th Edition):

Tran, Melissa Ann. “TREATMENT OF MELANOMA AND BREAST CANCER WITH GENETIC BASED LIPOSOMAL DRUG FORMULATIONS.” 2008. Web. 07 Apr 2020.

Vancouver:

Tran MA. TREATMENT OF MELANOMA AND BREAST CANCER WITH GENETIC BASED LIPOSOMAL DRUG FORMULATIONS. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2020 Apr 07]. Available from: https://etda.libraries.psu.edu/catalog/8430.

Council of Science Editors:

Tran MA. TREATMENT OF MELANOMA AND BREAST CANCER WITH GENETIC BASED LIPOSOMAL DRUG FORMULATIONS. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8430

8. Edmonston, Chad. Predicting transacting small RNA (ta-siRNA) and their Target Transcripts in the Emiliania Huxleyi Genome .

Degree: 2012, California State University – San Marcos

 Abstract Motivation: Small RNAs play an important role in regulating post-transcription gene expression. Trans-acting (ta-siRNAs) are a specific type of small RNA that inhibits gene… (more)

Subjects/Keywords: Bioinformatics; ta-siRNA; Emiliania Huxleyi

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APA (6th Edition):

Edmonston, C. (2012). Predicting transacting small RNA (ta-siRNA) and their Target Transcripts in the Emiliania Huxleyi Genome . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.8/205

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):

Edmonston, Chad. “Predicting transacting small RNA (ta-siRNA) and their Target Transcripts in the Emiliania Huxleyi Genome .” 2012. Thesis, California State University – San Marcos. Accessed April 07, 2020. http://hdl.handle.net/10211.8/205.

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

MLA Handbook (7th Edition):

Edmonston, Chad. “Predicting transacting small RNA (ta-siRNA) and their Target Transcripts in the Emiliania Huxleyi Genome .” 2012. Web. 07 Apr 2020.

Vancouver:

Edmonston C. Predicting transacting small RNA (ta-siRNA) and their Target Transcripts in the Emiliania Huxleyi Genome . [Internet] [Thesis]. California State University – San Marcos; 2012. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/10211.8/205.

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

Council of Science Editors:

Edmonston C. Predicting transacting small RNA (ta-siRNA) and their Target Transcripts in the Emiliania Huxleyi Genome . [Thesis]. California State University – San Marcos; 2012. Available from: http://hdl.handle.net/10211.8/205

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


University of Manchester

9. Dhami, Neha. Interference of central metabolism (TCA cycle) to influence CHO cell productivity.

Degree: 2017, University of Manchester

 This PhD project explored the role of tricarboxylic acid (TCA) cycle enzymes in regulating Chinese hamster ovary (CHO) cell metabolism with respect to growth and… (more)

Subjects/Keywords: CHO cells; TCA cycle; siRNA

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APA (6th Edition):

Dhami, N. (2017). Interference of central metabolism (TCA cycle) to influence CHO cell productivity. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307813

Chicago Manual of Style (16th Edition):

Dhami, Neha. “Interference of central metabolism (TCA cycle) to influence CHO cell productivity.” 2017. Doctoral Dissertation, University of Manchester. Accessed April 07, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307813.

MLA Handbook (7th Edition):

Dhami, Neha. “Interference of central metabolism (TCA cycle) to influence CHO cell productivity.” 2017. Web. 07 Apr 2020.

Vancouver:

Dhami N. Interference of central metabolism (TCA cycle) to influence CHO cell productivity. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2020 Apr 07]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307813.

Council of Science Editors:

Dhami N. Interference of central metabolism (TCA cycle) to influence CHO cell productivity. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307813

10. 김, 진엽. RNAi Screening-based Identification of USP10 as a Novel Regulator of Paraptosis.

Degree: 2018, Ajou University

Accumulating reports demonstrate the innate and acquired resistance of malignant cancer cells to apoptosis and apoptosis does not explain all the effects of cancer therapy.… (more)

Subjects/Keywords: siRNA screening; Paraptosis; Mitochondria; USP10

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APA (6th Edition):

김, . (2018). RNAi Screening-based Identification of USP10 as a Novel Regulator of Paraptosis. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/16586 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027611

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):

김, 진엽. “RNAi Screening-based Identification of USP10 as a Novel Regulator of Paraptosis.” 2018. Thesis, Ajou University. Accessed April 07, 2020. http://repository.ajou.ac.kr/handle/201003/16586 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027611.

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

MLA Handbook (7th Edition):

김, 진엽. “RNAi Screening-based Identification of USP10 as a Novel Regulator of Paraptosis.” 2018. Web. 07 Apr 2020.

Vancouver:

김 . RNAi Screening-based Identification of USP10 as a Novel Regulator of Paraptosis. [Internet] [Thesis]. Ajou University; 2018. [cited 2020 Apr 07]. Available from: http://repository.ajou.ac.kr/handle/201003/16586 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027611.

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

Council of Science Editors:

김 . RNAi Screening-based Identification of USP10 as a Novel Regulator of Paraptosis. [Thesis]. Ajou University; 2018. Available from: http://repository.ajou.ac.kr/handle/201003/16586 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000027611

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


University of Manchester

11. Frede, Annika. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.

Degree: 2016, University of Manchester

 In this thesis nanoparticles consisting of a calcium phosphate core encapsulated by poly(lactic-co-glycolic) acid and polyethylenimine were developed for the delivery of siRNA in vivo.… (more)

Subjects/Keywords: siRNA delivery; nanoparticles; IBD; COPD

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APA (6th Edition):

Frede, A. (2016). Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897

Chicago Manual of Style (16th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 07, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897.

MLA Handbook (7th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Web. 07 Apr 2020.

Vancouver:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Apr 07]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897.

Council of Science Editors:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301897


University of Cambridge

12. Yu, Qijia. Identification of regulators in autophagosome formation using image-based siRNA screening.

Degree: PhD, 2017, University of Cambridge

 Autophagy, referring to macroautophagy, is an evolutionarily conserved degradation pathway. Through autophagy cells can degrade damaged organelles, lipid vesicles and misfolded protein aggregates with implications… (more)

Subjects/Keywords: Autophagy; siRNA screening; Autophagosome formation

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APA (6th Edition):

Yu, Q. (2017). Identification of regulators in autophagosome formation using image-based siRNA screening. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267912

Chicago Manual of Style (16th Edition):

Yu, Qijia. “Identification of regulators in autophagosome formation using image-based siRNA screening.” 2017. Doctoral Dissertation, University of Cambridge. Accessed April 07, 2020. https://www.repository.cam.ac.uk/handle/1810/267912.

MLA Handbook (7th Edition):

Yu, Qijia. “Identification of regulators in autophagosome formation using image-based siRNA screening.” 2017. Web. 07 Apr 2020.

Vancouver:

Yu Q. Identification of regulators in autophagosome formation using image-based siRNA screening. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Apr 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/267912.

Council of Science Editors:

Yu Q. Identification of regulators in autophagosome formation using image-based siRNA screening. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267912


Cornell University

13. Pelet, Jeisa. Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation .

Degree: 2011, Cornell University

 Gene therapy has emerged as a promising technique to treat many chronic diseases, genetic disorders and even cancer. Furthermore, the recent discovery that RNA interference… (more)

Subjects/Keywords: polymers; combinatorial libraries; siRNA delivery

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APA (6th Edition):

Pelet, J. (2011). Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/29360

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):

Pelet, Jeisa. “Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation .” 2011. Thesis, Cornell University. Accessed April 07, 2020. http://hdl.handle.net/1813/29360.

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

MLA Handbook (7th Edition):

Pelet, Jeisa. “Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation .” 2011. Web. 07 Apr 2020.

Vancouver:

Pelet J. Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation . [Internet] [Thesis]. Cornell University; 2011. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/1813/29360.

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

Council of Science Editors:

Pelet J. Combinatorial Libraries Of Polymeric Vectors For Sirna Delivery: Synthesis, Characterization And In Vitro Evaluation . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29360

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


Vanderbilt University

14. Nelson, Christopher Edward. Sustained local delivery of siRNA from an injectable scaffold.

Degree: MS, Biomedical Engineering, 2011, Vanderbilt University

 Controlled gene silencing technologies have significant, unrealized potential for use in tissue regeneration applications. The design described herein provides a means to package and protect… (more)

Subjects/Keywords: controlled release; RNAi; polyurethane; siRNA

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

APA (6th Edition):

Nelson, C. E. (2011). Sustained local delivery of siRNA from an injectable scaffold. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;

Chicago Manual of Style (16th Edition):

Nelson, Christopher Edward. “Sustained local delivery of siRNA from an injectable scaffold.” 2011. Masters Thesis, Vanderbilt University. Accessed April 07, 2020. http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;.

MLA Handbook (7th Edition):

Nelson, Christopher Edward. “Sustained local delivery of siRNA from an injectable scaffold.” 2011. Web. 07 Apr 2020.

Vancouver:

Nelson CE. Sustained local delivery of siRNA from an injectable scaffold. [Internet] [Masters thesis]. Vanderbilt University; 2011. [cited 2020 Apr 07]. Available from: http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;.

Council of Science Editors:

Nelson CE. Sustained local delivery of siRNA from an injectable scaffold. [Masters Thesis]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu//available/etd-10272011-113508/ ;


University of Manchester

15. Frede, Annika. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.

Degree: PhD, 2016, University of Manchester

 In this thesis nanoparticles consisting of a calcium phosphate core encapsulated by poly(lactic-co-glycolic) acid and polyethylenimine were developed for the delivery of siRNA in vivo.… (more)

Subjects/Keywords: siRNA delivery; nanoparticles; IBD; COPD

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APA (6th Edition):

Frede, A. (2016). Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458

Chicago Manual of Style (16th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Doctoral Dissertation, University of Manchester. Accessed April 07, 2020. https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458.

MLA Handbook (7th Edition):

Frede, Annika. “Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery.” 2016. Web. 07 Apr 2020.

Vancouver:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2020 Apr 07]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458.

Council of Science Editors:

Frede A. Modulation of inflammatory responses at mucosal surfaces by nanoparticle-based siRNA delivery. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modulation-of-inflammatory-responses-at-mucosal-surfaces-by-nanoparticlebased-sirna-delivery(188e5303-0b29-4d14-8635-7d1fcf448270).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764458


University of Bath

16. Metwally, Abdelkader. Pharmaceutical formulations of bionanoparticles for siRNA delivery.

Degree: PhD, 2012, University of Bath

 The aims of this thesis are to design and synthesize non-viral cationic lipid vectors based on spermine, for the intracellular delivery of siRNA (short interfering… (more)

Subjects/Keywords: 572.88; siRNA; spermine; Nanoparticles

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APA (6th Edition):

Metwally, A. (2012). Pharmaceutical formulations of bionanoparticles for siRNA delivery. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/pharmaceutical-formulations-of-bionanoparticles-for-sirna-delivery(4eb42130-7545-477c-9d33-6f160ba0e247).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.557824

Chicago Manual of Style (16th Edition):

Metwally, Abdelkader. “Pharmaceutical formulations of bionanoparticles for siRNA delivery.” 2012. Doctoral Dissertation, University of Bath. Accessed April 07, 2020. https://researchportal.bath.ac.uk/en/studentthesis/pharmaceutical-formulations-of-bionanoparticles-for-sirna-delivery(4eb42130-7545-477c-9d33-6f160ba0e247).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.557824.

MLA Handbook (7th Edition):

Metwally, Abdelkader. “Pharmaceutical formulations of bionanoparticles for siRNA delivery.” 2012. Web. 07 Apr 2020.

Vancouver:

Metwally A. Pharmaceutical formulations of bionanoparticles for siRNA delivery. [Internet] [Doctoral dissertation]. University of Bath; 2012. [cited 2020 Apr 07]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/pharmaceutical-formulations-of-bionanoparticles-for-sirna-delivery(4eb42130-7545-477c-9d33-6f160ba0e247).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.557824.

Council of Science Editors:

Metwally A. Pharmaceutical formulations of bionanoparticles for siRNA delivery. [Doctoral Dissertation]. University of Bath; 2012. Available from: https://researchportal.bath.ac.uk/en/studentthesis/pharmaceutical-formulations-of-bionanoparticles-for-sirna-delivery(4eb42130-7545-477c-9d33-6f160ba0e247).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.557824

17. CASSIDY, PAUL SIMON. Targeting the tight-junctions of the conventional outflow pathway in primary open-angle glaucoma.

Degree: School of Genetics & Microbiology. Discipline of Genetics, 2018, Trinity College Dublin

 Primary open-angle glaucoma (POAG) is one of the leading causes of blindness worldwide, affecting an estimated 44.1 million people (Tham et al. 2014). POAG is… (more)

Subjects/Keywords: Glaucoma siRNA tight-junction outflow

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APA (6th Edition):

CASSIDY, P. S. (2018). Targeting the tight-junctions of the conventional outflow pathway in primary open-angle glaucoma. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/82279

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):

CASSIDY, PAUL SIMON. “Targeting the tight-junctions of the conventional outflow pathway in primary open-angle glaucoma.” 2018. Thesis, Trinity College Dublin. Accessed April 07, 2020. http://hdl.handle.net/2262/82279.

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

MLA Handbook (7th Edition):

CASSIDY, PAUL SIMON. “Targeting the tight-junctions of the conventional outflow pathway in primary open-angle glaucoma.” 2018. Web. 07 Apr 2020.

Vancouver:

CASSIDY PS. Targeting the tight-junctions of the conventional outflow pathway in primary open-angle glaucoma. [Internet] [Thesis]. Trinity College Dublin; 2018. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/2262/82279.

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

Council of Science Editors:

CASSIDY PS. Targeting the tight-junctions of the conventional outflow pathway in primary open-angle glaucoma. [Thesis]. Trinity College Dublin; 2018. Available from: http://hdl.handle.net/2262/82279

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


University of Ontario Institute of Technology

18. Hagen, Gordon. Synthesis and in vitro assessment of chemically modified siRNAs targeting BCL2 that contain 2'-ribose and triazole-linked backbone modifications.

Degree: 2015, University of Ontario Institute of Technology

 Short interfering RNAs (siRNAs) are biomolecules used for post-transcriptional gene regulation, and therefore hold promise as a future therapeutic by silencing gene expression of overexpressed… (more)

Subjects/Keywords: RNAi; siRNA; Chemical modification

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APA (6th Edition):

Hagen, G. (2015). Synthesis and in vitro assessment of chemically modified siRNAs targeting BCL2 that contain 2'-ribose and triazole-linked backbone modifications. (Thesis). University of Ontario Institute of Technology. Retrieved from http://hdl.handle.net/10155/563

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):

Hagen, Gordon. “Synthesis and in vitro assessment of chemically modified siRNAs targeting BCL2 that contain 2'-ribose and triazole-linked backbone modifications.” 2015. Thesis, University of Ontario Institute of Technology. Accessed April 07, 2020. http://hdl.handle.net/10155/563.

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

MLA Handbook (7th Edition):

Hagen, Gordon. “Synthesis and in vitro assessment of chemically modified siRNAs targeting BCL2 that contain 2'-ribose and triazole-linked backbone modifications.” 2015. Web. 07 Apr 2020.

Vancouver:

Hagen G. Synthesis and in vitro assessment of chemically modified siRNAs targeting BCL2 that contain 2'-ribose and triazole-linked backbone modifications. [Internet] [Thesis]. University of Ontario Institute of Technology; 2015. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/10155/563.

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

Council of Science Editors:

Hagen G. Synthesis and in vitro assessment of chemically modified siRNAs targeting BCL2 that contain 2'-ribose and triazole-linked backbone modifications. [Thesis]. University of Ontario Institute of Technology; 2015. Available from: http://hdl.handle.net/10155/563

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


University of Ontario Institute of Technology

19. Hammill, Matthew. The synthesis and in vitro evaluation of chemically modified siRNAs that contain internal azobenzene derivative spacers for selective and tunable photocontrol of activity.

Degree: 2017, University of Ontario Institute of Technology

 Short interfering RNAs (siRNAs) are biopolymers that are used as post-transcriptional gene regulators and as a natural endogenous defense against attack from viruses. These molecules… (more)

Subjects/Keywords: siRNA; Azobenzene; Photochemical; Reversible

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APA (6th Edition):

Hammill, M. (2017). The synthesis and in vitro evaluation of chemically modified siRNAs that contain internal azobenzene derivative spacers for selective and tunable photocontrol of activity. (Thesis). University of Ontario Institute of Technology. Retrieved from http://hdl.handle.net/10155/836

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):

Hammill, Matthew. “The synthesis and in vitro evaluation of chemically modified siRNAs that contain internal azobenzene derivative spacers for selective and tunable photocontrol of activity.” 2017. Thesis, University of Ontario Institute of Technology. Accessed April 07, 2020. http://hdl.handle.net/10155/836.

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

MLA Handbook (7th Edition):

Hammill, Matthew. “The synthesis and in vitro evaluation of chemically modified siRNAs that contain internal azobenzene derivative spacers for selective and tunable photocontrol of activity.” 2017. Web. 07 Apr 2020.

Vancouver:

Hammill M. The synthesis and in vitro evaluation of chemically modified siRNAs that contain internal azobenzene derivative spacers for selective and tunable photocontrol of activity. [Internet] [Thesis]. University of Ontario Institute of Technology; 2017. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/10155/836.

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

Council of Science Editors:

Hammill M. The synthesis and in vitro evaluation of chemically modified siRNAs that contain internal azobenzene derivative spacers for selective and tunable photocontrol of activity. [Thesis]. University of Ontario Institute of Technology; 2017. Available from: http://hdl.handle.net/10155/836

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


University of Ontario Institute of Technology

20. McKim, Christopher J. The synthesis and in vitro evaluation of short interfering RNAs that contain internal modified alkyl spacers.

Degree: 2014, University of Ontario Institute of Technology

 The ability to silence genes effectively at the pre-translational level through the use of short interfering ribonucleic acid (siRNA) has become a widely studied area… (more)

Subjects/Keywords: siRNA; Alkyl spacer; Chemical modification

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APA (6th Edition):

McKim, C. J. (2014). The synthesis and in vitro evaluation of short interfering RNAs that contain internal modified alkyl spacers. (Thesis). University of Ontario Institute of Technology. Retrieved from http://hdl.handle.net/10155/872

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):

McKim, Christopher J. “The synthesis and in vitro evaluation of short interfering RNAs that contain internal modified alkyl spacers.” 2014. Thesis, University of Ontario Institute of Technology. Accessed April 07, 2020. http://hdl.handle.net/10155/872.

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

MLA Handbook (7th Edition):

McKim, Christopher J. “The synthesis and in vitro evaluation of short interfering RNAs that contain internal modified alkyl spacers.” 2014. Web. 07 Apr 2020.

Vancouver:

McKim CJ. The synthesis and in vitro evaluation of short interfering RNAs that contain internal modified alkyl spacers. [Internet] [Thesis]. University of Ontario Institute of Technology; 2014. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/10155/872.

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

Council of Science Editors:

McKim CJ. The synthesis and in vitro evaluation of short interfering RNAs that contain internal modified alkyl spacers. [Thesis]. University of Ontario Institute of Technology; 2014. Available from: http://hdl.handle.net/10155/872

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


Texas State University – San Marcos

21. Palacios, Adriana S. Transfection Efficiencies of Chitosan/Sirna Nanoparticles in Colorectal Cancer Cells.

Degree: MS, Biochemistry, 2012, Texas State University – San Marcos

 RNA interference (RNAi) is a recently discovered phenomenon that employs the use of miRNA (microRNA) and siRNA (short interfering RNA) that can be utilized for… (more)

Subjects/Keywords: Transfection efficiency; siRNA; Chitosan nanoparticles

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APA (6th Edition):

Palacios, A. S. (2012). Transfection Efficiencies of Chitosan/Sirna Nanoparticles in Colorectal Cancer Cells. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/5487

Chicago Manual of Style (16th Edition):

Palacios, Adriana S. “Transfection Efficiencies of Chitosan/Sirna Nanoparticles in Colorectal Cancer Cells.” 2012. Masters Thesis, Texas State University – San Marcos. Accessed April 07, 2020. https://digital.library.txstate.edu/handle/10877/5487.

MLA Handbook (7th Edition):

Palacios, Adriana S. “Transfection Efficiencies of Chitosan/Sirna Nanoparticles in Colorectal Cancer Cells.” 2012. Web. 07 Apr 2020.

Vancouver:

Palacios AS. Transfection Efficiencies of Chitosan/Sirna Nanoparticles in Colorectal Cancer Cells. [Internet] [Masters thesis]. Texas State University – San Marcos; 2012. [cited 2020 Apr 07]. Available from: https://digital.library.txstate.edu/handle/10877/5487.

Council of Science Editors:

Palacios AS. Transfection Efficiencies of Chitosan/Sirna Nanoparticles in Colorectal Cancer Cells. [Masters Thesis]. Texas State University – San Marcos; 2012. Available from: https://digital.library.txstate.edu/handle/10877/5487

22. Castro, Fernanda Cavallari de. Silenciamento gênico do BMPRII em células da granulosa bovinas.

Degree: Mestrado, Qualidade e Produtividade Animal, 2014, University of São Paulo

As células da granulosa (CG) são constituintes do ambiente folicular de suma importância para o desenvolvimento, maturação e aquisição da competência oocitária, desempenhando funções como… (more)

Subjects/Keywords: BMP15; BMP15; GDF9; GDF9; Knockdown; Knockdown; Lipofecção; Lipofection; siRNA; siRNA

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

APA (6th Edition):

Castro, F. C. d. (2014). Silenciamento gênico do BMPRII em células da granulosa bovinas. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/74/74131/tde-23092014-110104/ ;

Chicago Manual of Style (16th Edition):

Castro, Fernanda Cavallari de. “Silenciamento gênico do BMPRII em células da granulosa bovinas.” 2014. Masters Thesis, University of São Paulo. Accessed April 07, 2020. http://www.teses.usp.br/teses/disponiveis/74/74131/tde-23092014-110104/ ;.

MLA Handbook (7th Edition):

Castro, Fernanda Cavallari de. “Silenciamento gênico do BMPRII em células da granulosa bovinas.” 2014. Web. 07 Apr 2020.

Vancouver:

Castro FCd. Silenciamento gênico do BMPRII em células da granulosa bovinas. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2020 Apr 07]. Available from: http://www.teses.usp.br/teses/disponiveis/74/74131/tde-23092014-110104/ ;.

Council of Science Editors:

Castro FCd. Silenciamento gênico do BMPRII em células da granulosa bovinas. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/74/74131/tde-23092014-110104/ ;


Johannes Gutenberg Universität Mainz

23. Krieg, Bettina Sarah. Evaluation of polymeric nanocarriers for RNA delivery.

Degree: 2014, Johannes Gutenberg Universität Mainz

Therapeutic RNAs, especially siRNAs, are a promising approach for treating diseases like cancer, neurodegenerative disorders and viral infections. Their application, however, is limited due to… (more)

Subjects/Keywords: siRNA; polyplexes; delivery; siRNA; Polyplexe; Transport; Natural sciences and mathematics

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APA (6th Edition):

Krieg, B. S. (2014). Evaluation of polymeric nanocarriers for RNA delivery. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/

Chicago Manual of Style (16th Edition):

Krieg, Bettina Sarah. “Evaluation of polymeric nanocarriers for RNA delivery.” 2014. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed April 07, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/.

MLA Handbook (7th Edition):

Krieg, Bettina Sarah. “Evaluation of polymeric nanocarriers for RNA delivery.” 2014. Web. 07 Apr 2020.

Vancouver:

Krieg BS. Evaluation of polymeric nanocarriers for RNA delivery. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2014. [cited 2020 Apr 07]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/.

Council of Science Editors:

Krieg BS. Evaluation of polymeric nanocarriers for RNA delivery. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2014. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2014/3922/


Johannes Gutenberg Universität Mainz

24. Osman Oglou, Okan. First contact imaging of nanoparticular siRNA – From synthesis to application of a prodye concept.

Degree: 2015, Johannes Gutenberg Universität Mainz

Delivery of therapeutic nucleic acid based drugs is still very demanding and difficult to manage and monitor. For this reason, a precise method for the… (more)

Subjects/Keywords: siRNA, Erstkontakt, Profluoreszenz; siRNA, nanoformulation, prodye, biolability,; Chemistry and allied sciences

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APA (6th Edition):

Osman Oglou, O. (2015). First contact imaging of nanoparticular siRNA – From synthesis to application of a prodye concept. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2015/4099/

Chicago Manual of Style (16th Edition):

Osman Oglou, Okan. “First contact imaging of nanoparticular siRNA – From synthesis to application of a prodye concept.” 2015. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed April 07, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2015/4099/.

MLA Handbook (7th Edition):

Osman Oglou, Okan. “First contact imaging of nanoparticular siRNA – From synthesis to application of a prodye concept.” 2015. Web. 07 Apr 2020.

Vancouver:

Osman Oglou O. First contact imaging of nanoparticular siRNA – From synthesis to application of a prodye concept. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2015. [cited 2020 Apr 07]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4099/.

Council of Science Editors:

Osman Oglou O. First contact imaging of nanoparticular siRNA – From synthesis to application of a prodye concept. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2015. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4099/


Université de Bordeaux I

25. Bui, Laurent. Assemblages de copolymères à blocs pour la vectorisation de siRNA : Study and simulation of model fluids and of pigment colours during paper coating by curtain coater.

Degree: Docteur es, Polymères, 2011, Université de Bordeaux I

Les « siRNA » sont des molécules double brin d’acide ribonucléique capables d’inhiber l’expression d’un gène spécifique, présentant ainsi un fort potentiel thérapeutique pour les… (more)

Subjects/Keywords: Copolymère; Amphiphile; Vectoristaion; SiRNA; Hyaluronate; Polysacharide; Copolymer; Amphiphilic; SiRNA

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APA (6th Edition):

Bui, L. (2011). Assemblages de copolymères à blocs pour la vectorisation de siRNA : Study and simulation of model fluids and of pigment colours during paper coating by curtain coater. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2011BOR14457

Chicago Manual of Style (16th Edition):

Bui, Laurent. “Assemblages de copolymères à blocs pour la vectorisation de siRNA : Study and simulation of model fluids and of pigment colours during paper coating by curtain coater.” 2011. Doctoral Dissertation, Université de Bordeaux I. Accessed April 07, 2020. http://www.theses.fr/2011BOR14457.

MLA Handbook (7th Edition):

Bui, Laurent. “Assemblages de copolymères à blocs pour la vectorisation de siRNA : Study and simulation of model fluids and of pigment colours during paper coating by curtain coater.” 2011. Web. 07 Apr 2020.

Vancouver:

Bui L. Assemblages de copolymères à blocs pour la vectorisation de siRNA : Study and simulation of model fluids and of pigment colours during paper coating by curtain coater. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2011. [cited 2020 Apr 07]. Available from: http://www.theses.fr/2011BOR14457.

Council of Science Editors:

Bui L. Assemblages de copolymères à blocs pour la vectorisation de siRNA : Study and simulation of model fluids and of pigment colours during paper coating by curtain coater. [Doctoral Dissertation]. Université de Bordeaux I; 2011. Available from: http://www.theses.fr/2011BOR14457


University of Alberta

26. Alshamsan, Aws. Development of stat-3 targeting siRNA nano-carriers for cancer therapy.

Degree: PhD, Faculty of Pharmacy and Pharmaceutical Sciences, 2010, University of Alberta

 In many tumors, persistently-active signal transducer and activator of transcription 3 (STAT3) imparts several oncogenic features such as survival, proliferation, angiogenesis, and immune escape. Therefore,… (more)

Subjects/Keywords: STAT-3; Cancer; siRNA; Nanomedicine; Drug Delivery

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APA (6th Edition):

Alshamsan, A. (2010). Development of stat-3 targeting siRNA nano-carriers for cancer therapy. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/fx719n70b

Chicago Manual of Style (16th Edition):

Alshamsan, Aws. “Development of stat-3 targeting siRNA nano-carriers for cancer therapy.” 2010. Doctoral Dissertation, University of Alberta. Accessed April 07, 2020. https://era.library.ualberta.ca/files/fx719n70b.

MLA Handbook (7th Edition):

Alshamsan, Aws. “Development of stat-3 targeting siRNA nano-carriers for cancer therapy.” 2010. Web. 07 Apr 2020.

Vancouver:

Alshamsan A. Development of stat-3 targeting siRNA nano-carriers for cancer therapy. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2020 Apr 07]. Available from: https://era.library.ualberta.ca/files/fx719n70b.

Council of Science Editors:

Alshamsan A. Development of stat-3 targeting siRNA nano-carriers for cancer therapy. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/fx719n70b


Case Western Reserve University

27. Zheng, Zijie. IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA.

Degree: MSs, Biomedical Engineering, 2015, Case Western Reserve University

 Cells adapt themselves to the dynamic extracellular environment by responding to numerous signal stimuli. Strategies for engineering stimulus-responsive biomaterials as drug delivery vehicles may mimic… (more)

Subjects/Keywords: Biomedical Engineering; siRNA, photodegradable, hydrogel, controlled release

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

APA (6th Edition):

Zheng, Z. (2015). IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306

Chicago Manual of Style (16th Edition):

Zheng, Zijie. “IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA.” 2015. Masters Thesis, Case Western Reserve University. Accessed April 07, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306.

MLA Handbook (7th Edition):

Zheng, Zijie. “IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA.” 2015. Web. 07 Apr 2020.

Vancouver:

Zheng Z. IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA. [Internet] [Masters thesis]. Case Western Reserve University; 2015. [cited 2020 Apr 07]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306.

Council of Science Editors:

Zheng Z. IN SITU FORMING PHOTODEGRADABLE HYDROGEL FOR CONTROLLED DELIVERY OF siRNA. [Masters Thesis]. Case Western Reserve University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1434560306


Texas A&M University

28. Shrestha, Ritu 1984-. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.

Degree: 2012, Texas A&M University

 Applications of nanotechnology in medicine, also known as nanomedicine, is a rapidly growing field as it holds great potential in the development of novel therapeutics… (more)

Subjects/Keywords: siRNA delivery; nanomedicine; endosomal escape; nanoparticles; Polymers

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APA (6th Edition):

Shrestha, R. 1. (2012). Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148332

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):

Shrestha, Ritu 1984-. “Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.” 2012. Thesis, Texas A&M University. Accessed April 07, 2020. http://hdl.handle.net/1969.1/148332.

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

MLA Handbook (7th Edition):

Shrestha, Ritu 1984-. “Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics.” 2012. Web. 07 Apr 2020.

Vancouver:

Shrestha R1. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2020 Apr 07]. Available from: http://hdl.handle.net/1969.1/148332.

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

Council of Science Editors:

Shrestha R1. Multi-functional Bio-synthetic Hybrid Nanostructures for Enhanced Cellular Uptake, Endosomal Escape and Targeted Delivery Toward Diagnostics and Therapeutics. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148332

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


Punjabi University

29. Singh, Shailendra. Design and development of a model for sequences and structure of biomolecules.

Degree: 2012, Punjabi University

In the recent past it was observed that a growing interest of computer professionals in the field of molecular biology has resulted into development of… (more)

Subjects/Keywords: Bioinformatics; Biomolecules; siRNA; Deoxyribonucleic acid; Ribonucleic acid

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

APA (6th Edition):

Singh, S. (2012). Design and development of a model for sequences and structure of biomolecules. (Thesis). Punjabi University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/3588

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):

Singh, Shailendra. “Design and development of a model for sequences and structure of biomolecules.” 2012. Thesis, Punjabi University. Accessed April 07, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/3588.

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

MLA Handbook (7th Edition):

Singh, Shailendra. “Design and development of a model for sequences and structure of biomolecules.” 2012. Web. 07 Apr 2020.

Vancouver:

Singh S. Design and development of a model for sequences and structure of biomolecules. [Internet] [Thesis]. Punjabi University; 2012. [cited 2020 Apr 07]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3588.

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

Council of Science Editors:

Singh S. Design and development of a model for sequences and structure of biomolecules. [Thesis]. Punjabi University; 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/3588

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

30. Fogarty, Stuart A. SMURF1 as a Novel Regulator of PGC-1a.

Degree: Biological Sciences - Cell and Molecular: M.S., Biology, 2016, St. Cloud State University

  Parkinson’s disease is a neurodegenerative disorder caused by the impairment and/or death of the dopaminergic neurons in the area of the brain that controls… (more)

Subjects/Keywords: SMURF1 CRISPR siRNA PGC-1 Parkinson's Regulator

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

APA (6th Edition):

Fogarty, S. A. (2016). SMURF1 as a Novel Regulator of PGC-1a. (Masters Thesis). St. Cloud State University. Retrieved from https://repository.stcloudstate.edu/biol_etds/9

Chicago Manual of Style (16th Edition):

Fogarty, Stuart A. “SMURF1 as a Novel Regulator of PGC-1a.” 2016. Masters Thesis, St. Cloud State University. Accessed April 07, 2020. https://repository.stcloudstate.edu/biol_etds/9.

MLA Handbook (7th Edition):

Fogarty, Stuart A. “SMURF1 as a Novel Regulator of PGC-1a.” 2016. Web. 07 Apr 2020.

Vancouver:

Fogarty SA. SMURF1 as a Novel Regulator of PGC-1a. [Internet] [Masters thesis]. St. Cloud State University; 2016. [cited 2020 Apr 07]. Available from: https://repository.stcloudstate.edu/biol_etds/9.

Council of Science Editors:

Fogarty SA. SMURF1 as a Novel Regulator of PGC-1a. [Masters Thesis]. St. Cloud State University; 2016. Available from: https://repository.stcloudstate.edu/biol_etds/9

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