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You searched for subject:(Autophagy). Showing records 1 – 30 of 989 total matches.

[1] [2] [3] [4] [5] … [33]

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University of Georgia

1. Nadal, Marina. Exploring the role of autophagy and cell wall degrading enzymes in the life cycle and pathogenic development of the basidiomycete fungal plant pathogen Ustilago maydis.

Degree: PhD, Plant Pathology, 2009, University of Georgia

 The plant pathogen Ustilago maydis, of the Basidiomycota is responsible for corn smut disease and an important model organism for this fungal phylum. One of… (more)

Subjects/Keywords: autophagy

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APA (6th Edition):

Nadal, M. (2009). Exploring the role of autophagy and cell wall degrading enzymes in the life cycle and pathogenic development of the basidiomycete fungal plant pathogen Ustilago maydis. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/nadal_marina_200912_phd

Chicago Manual of Style (16th Edition):

Nadal, Marina. “Exploring the role of autophagy and cell wall degrading enzymes in the life cycle and pathogenic development of the basidiomycete fungal plant pathogen Ustilago maydis.” 2009. Doctoral Dissertation, University of Georgia. Accessed February 19, 2020. http://purl.galileo.usg.edu/uga_etd/nadal_marina_200912_phd.

MLA Handbook (7th Edition):

Nadal, Marina. “Exploring the role of autophagy and cell wall degrading enzymes in the life cycle and pathogenic development of the basidiomycete fungal plant pathogen Ustilago maydis.” 2009. Web. 19 Feb 2020.

Vancouver:

Nadal M. Exploring the role of autophagy and cell wall degrading enzymes in the life cycle and pathogenic development of the basidiomycete fungal plant pathogen Ustilago maydis. [Internet] [Doctoral dissertation]. University of Georgia; 2009. [cited 2020 Feb 19]. Available from: http://purl.galileo.usg.edu/uga_etd/nadal_marina_200912_phd.

Council of Science Editors:

Nadal M. Exploring the role of autophagy and cell wall degrading enzymes in the life cycle and pathogenic development of the basidiomycete fungal plant pathogen Ustilago maydis. [Doctoral Dissertation]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/nadal_marina_200912_phd

2. Ladha, Feria A. Potential role for Human KCTD9 in the autophagy pathway: A novel autophagosome-associated protein.

Degree: 2014, Johns Hopkins University

 KCTD9 belongs to the human potassium channel tetramerization domain (KCTD) family and is of unknown biological function. Our studies in yeast showed that the yeast… (more)

Subjects/Keywords: KCTD9; Autophagy

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APA (6th Edition):

Ladha, F. A. (2014). Potential role for Human KCTD9 in the autophagy pathway: A novel autophagosome-associated protein. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37315

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):

Ladha, Feria A. “Potential role for Human KCTD9 in the autophagy pathway: A novel autophagosome-associated protein.” 2014. Thesis, Johns Hopkins University. Accessed February 19, 2020. http://jhir.library.jhu.edu/handle/1774.2/37315.

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

MLA Handbook (7th Edition):

Ladha, Feria A. “Potential role for Human KCTD9 in the autophagy pathway: A novel autophagosome-associated protein.” 2014. Web. 19 Feb 2020.

Vancouver:

Ladha FA. Potential role for Human KCTD9 in the autophagy pathway: A novel autophagosome-associated protein. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2020 Feb 19]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37315.

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

Council of Science Editors:

Ladha FA. Potential role for Human KCTD9 in the autophagy pathway: A novel autophagosome-associated protein. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/37315

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

3. 平井, 慎一郎. 2-Phenyl-APB-144を用いたラット網膜色素上皮変性メカニズムに関する研究 : Research on mechanism of rat retinal pigment epithelium degeneration induced by 2-Phenyl-APB-144; 2-Phenyl-APB-144 オ モチイタ ラット モウマク シキソ ジョウヒ ヘンセイ メカニズム ニ カンスル ケンキュウ.

Degree: 博士(バイオサイエンス), Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: autophagy

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APA (6th Edition):

平井, . (n.d.). 2-Phenyl-APB-144を用いたラット網膜色素上皮変性メカニズムに関する研究 : Research on mechanism of rat retinal pigment epithelium degeneration induced by 2-Phenyl-APB-144; 2-Phenyl-APB-144 オ モチイタ ラット モウマク シキソ ジョウヒ ヘンセイ メカニズム ニ カンスル ケンキュウ. (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/10061/10436

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):

平井, 慎一郎. “2-Phenyl-APB-144を用いたラット網膜色素上皮変性メカニズムに関する研究 : Research on mechanism of rat retinal pigment epithelium degeneration induced by 2-Phenyl-APB-144; 2-Phenyl-APB-144 オ モチイタ ラット モウマク シキソ ジョウヒ ヘンセイ メカニズム ニ カンスル ケンキュウ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed February 19, 2020. http://hdl.handle.net/10061/10436.

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):

平井, 慎一郎. “2-Phenyl-APB-144を用いたラット網膜色素上皮変性メカニズムに関する研究 : Research on mechanism of rat retinal pigment epithelium degeneration induced by 2-Phenyl-APB-144; 2-Phenyl-APB-144 オ モチイタ ラット モウマク シキソ ジョウヒ ヘンセイ メカニズム ニ カンスル ケンキュウ.” Web. 19 Feb 2020.

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

Vancouver:

平井 . 2-Phenyl-APB-144を用いたラット網膜色素上皮変性メカニズムに関する研究 : Research on mechanism of rat retinal pigment epithelium degeneration induced by 2-Phenyl-APB-144; 2-Phenyl-APB-144 オ モチイタ ラット モウマク シキソ ジョウヒ ヘンセイ メカニズム ニ カンスル ケンキュウ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10061/10436.

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:

平井 . 2-Phenyl-APB-144を用いたラット網膜色素上皮変性メカニズムに関する研究 : Research on mechanism of rat retinal pigment epithelium degeneration induced by 2-Phenyl-APB-144; 2-Phenyl-APB-144 オ モチイタ ラット モウマク シキソ ジョウヒ ヘンセイ メカニズム ニ カンスル ケンキュウ. [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/10061/10436

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


Victoria University of Wellington

4. Vithal, Tanisha. Investigating the function of CLU in Alzheimer's Disease in in vitro and in vivo models.

Degree: 2016, Victoria University of Wellington

 Alzheimer’s disease (AD) is a neurodegenerative disease that is responsible for 50-80% of dementia cases and is characterised by lack of visuospatial perception, impairment of… (more)

Subjects/Keywords: Clusterin; Cholesterol; Autophagy

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APA (6th Edition):

Vithal, T. (2016). Investigating the function of CLU in Alzheimer's Disease in in vitro and in vivo models. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/5050

Chicago Manual of Style (16th Edition):

Vithal, Tanisha. “Investigating the function of CLU in Alzheimer's Disease in in vitro and in vivo models.” 2016. Masters Thesis, Victoria University of Wellington. Accessed February 19, 2020. http://hdl.handle.net/10063/5050.

MLA Handbook (7th Edition):

Vithal, Tanisha. “Investigating the function of CLU in Alzheimer's Disease in in vitro and in vivo models.” 2016. Web. 19 Feb 2020.

Vancouver:

Vithal T. Investigating the function of CLU in Alzheimer's Disease in in vitro and in vivo models. [Internet] [Masters thesis]. Victoria University of Wellington; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10063/5050.

Council of Science Editors:

Vithal T. Investigating the function of CLU in Alzheimer's Disease in in vitro and in vivo models. [Masters Thesis]. Victoria University of Wellington; 2016. Available from: http://hdl.handle.net/10063/5050


University of Illinois – Urbana-Champaign

5. Wang, Huan. Autophagy: activation, function and regulation by a protein restricted diet during pregnancy and lactation.

Degree: PhD, Food Science & Human Nutrition, 2015, University of Illinois – Urbana-Champaign

 Developmental protein restriction is associated with numerous diseases including obesity, diabetes and cardiovascular disease, both in the mother and offspring. Recent intensive research efforts have… (more)

Subjects/Keywords: Low protein; Autophagy

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APA (6th Edition):

Wang, H. (2015). Autophagy: activation, function and regulation by a protein restricted diet during pregnancy and lactation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/89270

Chicago Manual of Style (16th Edition):

Wang, Huan. “Autophagy: activation, function and regulation by a protein restricted diet during pregnancy and lactation.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed February 19, 2020. http://hdl.handle.net/2142/89270.

MLA Handbook (7th Edition):

Wang, Huan. “Autophagy: activation, function and regulation by a protein restricted diet during pregnancy and lactation.” 2015. Web. 19 Feb 2020.

Vancouver:

Wang H. Autophagy: activation, function and regulation by a protein restricted diet during pregnancy and lactation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/2142/89270.

Council of Science Editors:

Wang H. Autophagy: activation, function and regulation by a protein restricted diet during pregnancy and lactation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/89270


Universiteit Utrecht

6. Wang, Z. The Role of Autophagy and its Inhibition in Cancer Treatment.

Degree: 2012, Universiteit Utrecht

Autophagy serves as a simple garbage disposal mechanism to eliminate damaged and outdated components from cells so as to maintain cellular homeostasis.Autophagy defects have been… (more)

Subjects/Keywords: autophagy; cancer; inhibition

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APA (6th Edition):

Wang, Z. (2012). The Role of Autophagy and its Inhibition in Cancer Treatment. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/253751

Chicago Manual of Style (16th Edition):

Wang, Z. “The Role of Autophagy and its Inhibition in Cancer Treatment.” 2012. Masters Thesis, Universiteit Utrecht. Accessed February 19, 2020. http://dspace.library.uu.nl:8080/handle/1874/253751.

MLA Handbook (7th Edition):

Wang, Z. “The Role of Autophagy and its Inhibition in Cancer Treatment.” 2012. Web. 19 Feb 2020.

Vancouver:

Wang Z. The Role of Autophagy and its Inhibition in Cancer Treatment. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2020 Feb 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/253751.

Council of Science Editors:

Wang Z. The Role of Autophagy and its Inhibition in Cancer Treatment. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/253751


Vanderbilt University

7. Eby, Kathryn Grace. Identification and Characterization of p53 Target Genes.

Degree: PhD, Biochemistry, 2010, Vanderbilt University

 After 30 years of research, p53 is recognized as one of the most frequently mutated genes in human cancer (Baker et al, 1989; Nigro et… (more)

Subjects/Keywords: ISG20L1; p53; autophagy

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APA (6th Edition):

Eby, K. G. (2010). Identification and Characterization of p53 Target Genes. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;

Chicago Manual of Style (16th Edition):

Eby, Kathryn Grace. “Identification and Characterization of p53 Target Genes.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed February 19, 2020. http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;.

MLA Handbook (7th Edition):

Eby, Kathryn Grace. “Identification and Characterization of p53 Target Genes.” 2010. Web. 19 Feb 2020.

Vancouver:

Eby KG. Identification and Characterization of p53 Target Genes. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2020 Feb 19]. Available from: http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;.

Council of Science Editors:

Eby KG. Identification and Characterization of p53 Target Genes. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;


University of Guelph

8. Preiss, Richard. Autophagy Gene Overexpression in Saccharomyces cerevisiae for Accelerated Sparkling Wine Production .

Degree: 2017, University of Guelph

 Traditional sparkling wines are the product of carbonation and aging of a base wine with yeast in the bottle, where yeast cell compounds are released… (more)

Subjects/Keywords: autophagy; wine; autolysis

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APA (6th Edition):

Preiss, R. (2017). Autophagy Gene Overexpression in Saccharomyces cerevisiae for Accelerated Sparkling Wine Production . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10469

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):

Preiss, Richard. “Autophagy Gene Overexpression in Saccharomyces cerevisiae for Accelerated Sparkling Wine Production .” 2017. Thesis, University of Guelph. Accessed February 19, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10469.

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

MLA Handbook (7th Edition):

Preiss, Richard. “Autophagy Gene Overexpression in Saccharomyces cerevisiae for Accelerated Sparkling Wine Production .” 2017. Web. 19 Feb 2020.

Vancouver:

Preiss R. Autophagy Gene Overexpression in Saccharomyces cerevisiae for Accelerated Sparkling Wine Production . [Internet] [Thesis]. University of Guelph; 2017. [cited 2020 Feb 19]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10469.

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

Council of Science Editors:

Preiss R. Autophagy Gene Overexpression in Saccharomyces cerevisiae for Accelerated Sparkling Wine Production . [Thesis]. University of Guelph; 2017. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10469

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


University of Guelph

9. Pereira, Leanne. THE ROLE OF A DEFECT IN THE CDP-ETHANOLAMINE PATHWAY IN AUTOPHAGY .

Degree: 2012, University of Guelph

Autophagy is the process that degrades cytosolic constituents into products that can be recycled for use in energy generation and other processes. The endoplasmic reticulum… (more)

Subjects/Keywords: Autophagy; Kennedy Pathway

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APA (6th Edition):

Pereira, L. (2012). THE ROLE OF A DEFECT IN THE CDP-ETHANOLAMINE PATHWAY IN AUTOPHAGY . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4845

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):

Pereira, Leanne. “THE ROLE OF A DEFECT IN THE CDP-ETHANOLAMINE PATHWAY IN AUTOPHAGY .” 2012. Thesis, University of Guelph. Accessed February 19, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4845.

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

MLA Handbook (7th Edition):

Pereira, Leanne. “THE ROLE OF A DEFECT IN THE CDP-ETHANOLAMINE PATHWAY IN AUTOPHAGY .” 2012. Web. 19 Feb 2020.

Vancouver:

Pereira L. THE ROLE OF A DEFECT IN THE CDP-ETHANOLAMINE PATHWAY IN AUTOPHAGY . [Internet] [Thesis]. University of Guelph; 2012. [cited 2020 Feb 19]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4845.

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

Council of Science Editors:

Pereira L. THE ROLE OF A DEFECT IN THE CDP-ETHANOLAMINE PATHWAY IN AUTOPHAGY . [Thesis]. University of Guelph; 2012. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/4845

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


Dalhousie University

10. Cyr, David P. KSHV vGPCR: A VIRAL ONCOPROTEIN THAT TRIGGERS AUTOPHAGY AND CELLULAR SENESCENCE.

Degree: MS, Department of Microbiology & Immunology, 2013, Dalhousie University

Autophagy (literally to ‘self-eat’) is an intracellular, catabolic mechanism to degrade and recycle cytoplasmic contents in response to metabolic, oxidative, and genotoxic stresses. Autophagy plays… (more)

Subjects/Keywords: KSHV; vGPCR; autophagy; senescence

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APA (6th Edition):

Cyr, D. P. (2013). KSHV vGPCR: A VIRAL ONCOPROTEIN THAT TRIGGERS AUTOPHAGY AND CELLULAR SENESCENCE. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/36316

Chicago Manual of Style (16th Edition):

Cyr, David P. “KSHV vGPCR: A VIRAL ONCOPROTEIN THAT TRIGGERS AUTOPHAGY AND CELLULAR SENESCENCE.” 2013. Masters Thesis, Dalhousie University. Accessed February 19, 2020. http://hdl.handle.net/10222/36316.

MLA Handbook (7th Edition):

Cyr, David P. “KSHV vGPCR: A VIRAL ONCOPROTEIN THAT TRIGGERS AUTOPHAGY AND CELLULAR SENESCENCE.” 2013. Web. 19 Feb 2020.

Vancouver:

Cyr DP. KSHV vGPCR: A VIRAL ONCOPROTEIN THAT TRIGGERS AUTOPHAGY AND CELLULAR SENESCENCE. [Internet] [Masters thesis]. Dalhousie University; 2013. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10222/36316.

Council of Science Editors:

Cyr DP. KSHV vGPCR: A VIRAL ONCOPROTEIN THAT TRIGGERS AUTOPHAGY AND CELLULAR SENESCENCE. [Masters Thesis]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/36316

11. Sing, Cierra Nicole. Role for the ESCRT complex in the relationship between nutrient signaling and autophagy in Saccharyomyces cerevisae.

Degree: 2014, Johns Hopkins University

 Nutrient sensing is a vital cellular pathway used by all organisms to synchronize their cellular proliferation to correspond with their nutritional status through TOR (target… (more)

Subjects/Keywords: ESCRT; Nutrient sensing; Autophagy

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APA (6th Edition):

Sing, C. N. (2014). Role for the ESCRT complex in the relationship between nutrient signaling and autophagy in Saccharyomyces cerevisae. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37259

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):

Sing, Cierra Nicole. “Role for the ESCRT complex in the relationship between nutrient signaling and autophagy in Saccharyomyces cerevisae.” 2014. Thesis, Johns Hopkins University. Accessed February 19, 2020. http://jhir.library.jhu.edu/handle/1774.2/37259.

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

MLA Handbook (7th Edition):

Sing, Cierra Nicole. “Role for the ESCRT complex in the relationship between nutrient signaling and autophagy in Saccharyomyces cerevisae.” 2014. Web. 19 Feb 2020.

Vancouver:

Sing CN. Role for the ESCRT complex in the relationship between nutrient signaling and autophagy in Saccharyomyces cerevisae. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2020 Feb 19]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37259.

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

Council of Science Editors:

Sing CN. Role for the ESCRT complex in the relationship between nutrient signaling and autophagy in Saccharyomyces cerevisae. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/37259

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


University of Edinburgh

12. Paro, Simona. RNA editing and autophagy in Drosophila melanogaster.

Degree: PhD, 2012, University of Edinburgh

 Post-transcriptional regulation of gene expression involves a diverse set of mechanisms such as RNA splicing, RNA localization, and RNA turn-over. Adenosine to Inosine (A-to-I) RNA… (more)

Subjects/Keywords: 572.8; RNA editing; autophagy

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APA (6th Edition):

Paro, S. (2012). RNA editing and autophagy in Drosophila melanogaster. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8254

Chicago Manual of Style (16th Edition):

Paro, Simona. “RNA editing and autophagy in Drosophila melanogaster.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed February 19, 2020. http://hdl.handle.net/1842/8254.

MLA Handbook (7th Edition):

Paro, Simona. “RNA editing and autophagy in Drosophila melanogaster.” 2012. Web. 19 Feb 2020.

Vancouver:

Paro S. RNA editing and autophagy in Drosophila melanogaster. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/1842/8254.

Council of Science Editors:

Paro S. RNA editing and autophagy in Drosophila melanogaster. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/8254


University of Missouri – Columbia

13. Morales Quiñones, Mariana. A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast.

Degree: 2011, University of Missouri – Columbia

 Misfolded protein aggregation causes disease and aging; autophagy counteracts this by eliminating damaged components, enabling cells to survive starvation. The Cytoplasm-to-vacuole-targeting (Cvt) pathway in yeast… (more)

Subjects/Keywords: aminopeptidase; autophagy; propeptide; protein aggregation

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APA (6th Edition):

Morales Quiñones, M. (2011). A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/14442

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):

Morales Quiñones, Mariana. “A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast.” 2011. Thesis, University of Missouri – Columbia. Accessed February 19, 2020. http://hdl.handle.net/10355/14442.

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

MLA Handbook (7th Edition):

Morales Quiñones, Mariana. “A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast.” 2011. Web. 19 Feb 2020.

Vancouver:

Morales Quiñones M. A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast. [Internet] [Thesis]. University of Missouri – Columbia; 2011. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10355/14442.

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

Council of Science Editors:

Morales Quiñones M. A unique way to form a vesicle: aminopeptidase 1 aggregation and its binding to receptor ATG19 for recruitment of autophagic proteins to form a vesicle in the cytoplasm-to-vacuole-targeting pathway in yeast. [Thesis]. University of Missouri – Columbia; 2011. Available from: http://hdl.handle.net/10355/14442

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


University of Minnesota

14. Otto, Neil. Exploring The Interactions And Functions Of The ULK1 Complex In The Autophagy Pathway.

Degree: PhD, Biochemistry, Molecular Bio, and Biophysics, 2014, University of Minnesota

Autophagy, an evolutionarily conserved process through which cellular components or organelles are degraded through lysosomes, is induced when eukaryotic cells are under nutrient starvation or… (more)

Subjects/Keywords: Atg13; Atg8; Autophagy; LIR; ULK1

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APA (6th Edition):

Otto, N. (2014). Exploring The Interactions And Functions Of The ULK1 Complex In The Autophagy Pathway. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/178934

Chicago Manual of Style (16th Edition):

Otto, Neil. “Exploring The Interactions And Functions Of The ULK1 Complex In The Autophagy Pathway.” 2014. Doctoral Dissertation, University of Minnesota. Accessed February 19, 2020. http://hdl.handle.net/11299/178934.

MLA Handbook (7th Edition):

Otto, Neil. “Exploring The Interactions And Functions Of The ULK1 Complex In The Autophagy Pathway.” 2014. Web. 19 Feb 2020.

Vancouver:

Otto N. Exploring The Interactions And Functions Of The ULK1 Complex In The Autophagy Pathway. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/11299/178934.

Council of Science Editors:

Otto N. Exploring The Interactions And Functions Of The ULK1 Complex In The Autophagy Pathway. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/178934


University of Minnesota

15. SUN, LEISHENG. Interactions between Human Two-pore Channels and Nonaspanin Proteins.

Degree: MS, Pharmacology, 2016, University of Minnesota

Autophagy is an evolutionary conserved lysosomal degradation pathway which is involved with a variety of cellular process, but the relevant mechanisms remain elusive. Here I… (more)

Subjects/Keywords: Autophagy; Nonaspanins; Two-pore channel

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APA (6th Edition):

SUN, L. (2016). Interactions between Human Two-pore Channels and Nonaspanin Proteins. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/182714

Chicago Manual of Style (16th Edition):

SUN, LEISHENG. “Interactions between Human Two-pore Channels and Nonaspanin Proteins.” 2016. Masters Thesis, University of Minnesota. Accessed February 19, 2020. http://hdl.handle.net/11299/182714.

MLA Handbook (7th Edition):

SUN, LEISHENG. “Interactions between Human Two-pore Channels and Nonaspanin Proteins.” 2016. Web. 19 Feb 2020.

Vancouver:

SUN L. Interactions between Human Two-pore Channels and Nonaspanin Proteins. [Internet] [Masters thesis]. University of Minnesota; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/11299/182714.

Council of Science Editors:

SUN L. Interactions between Human Two-pore Channels and Nonaspanin Proteins. [Masters Thesis]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/182714


University of New Mexico

16. Dinkins, Christina. Roles of autophagy in HIV-1 infection.

Degree: Biomedical Sciences Graduate Program, 2011, University of New Mexico

 Human immunodeficiency virus type 1 (HIV-1) chronically infects approximately 30 million people worldwide. HIV-1 has become one of the most difficult viral infections to treat… (more)

Subjects/Keywords: autophagy; HIV; Nef; RhTRIM5╬▒

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APA (6th Edition):

Dinkins, C. (2011). Roles of autophagy in HIV-1 infection. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/37

Chicago Manual of Style (16th Edition):

Dinkins, Christina. “Roles of autophagy in HIV-1 infection.” 2011. Doctoral Dissertation, University of New Mexico. Accessed February 19, 2020. https://digitalrepository.unm.edu/biom_etds/37.

MLA Handbook (7th Edition):

Dinkins, Christina. “Roles of autophagy in HIV-1 infection.” 2011. Web. 19 Feb 2020.

Vancouver:

Dinkins C. Roles of autophagy in HIV-1 infection. [Internet] [Doctoral dissertation]. University of New Mexico; 2011. [cited 2020 Feb 19]. Available from: https://digitalrepository.unm.edu/biom_etds/37.

Council of Science Editors:

Dinkins C. Roles of autophagy in HIV-1 infection. [Doctoral Dissertation]. University of New Mexico; 2011. Available from: https://digitalrepository.unm.edu/biom_etds/37


University of New Mexico

17. Jiang, Shanya. MOLECULAR MECHANISM OF AUTOPHAGY-BASED UNCONVENTIONAL SECRETION OF IL-β.

Degree: Biomedical Sciences Graduate Program, 2014, University of New Mexico

 Proteins without signal peptides can still be released into extracellular space via ER/Golgi-independent unconventional secretory pathway(s) that remain to be revealed. A class of leaderless… (more)

Subjects/Keywords: Autophagy; Unconventional Secretion; IL-β

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APA (6th Edition):

Jiang, S. (2014). MOLECULAR MECHANISM OF AUTOPHAGY-BASED UNCONVENTIONAL SECRETION OF IL-β. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/130

Chicago Manual of Style (16th Edition):

Jiang, Shanya. “MOLECULAR MECHANISM OF AUTOPHAGY-BASED UNCONVENTIONAL SECRETION OF IL-β.” 2014. Doctoral Dissertation, University of New Mexico. Accessed February 19, 2020. https://digitalrepository.unm.edu/biom_etds/130.

MLA Handbook (7th Edition):

Jiang, Shanya. “MOLECULAR MECHANISM OF AUTOPHAGY-BASED UNCONVENTIONAL SECRETION OF IL-β.” 2014. Web. 19 Feb 2020.

Vancouver:

Jiang S. MOLECULAR MECHANISM OF AUTOPHAGY-BASED UNCONVENTIONAL SECRETION OF IL-β. [Internet] [Doctoral dissertation]. University of New Mexico; 2014. [cited 2020 Feb 19]. Available from: https://digitalrepository.unm.edu/biom_etds/130.

Council of Science Editors:

Jiang S. MOLECULAR MECHANISM OF AUTOPHAGY-BASED UNCONVENTIONAL SECRETION OF IL-β. [Doctoral Dissertation]. University of New Mexico; 2014. Available from: https://digitalrepository.unm.edu/biom_etds/130


University of Rochester

18. Chesser, Adrianne S. Selectively Enhancing the Clearance of Pathological Tau Through the Use of Phytochemical Compounds.

Degree: PhD, 2015, University of Rochester

 Alzheimer disease (AD) is the leading cause of neurodegeneration worldwide. Unfortunately, there are limited therapeutic options, due in part to an incomplete understanding of disease… (more)

Subjects/Keywords: Alzheimer Disease; Tau; Autophagy; EGCG

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APA (6th Edition):

Chesser, A. S. (2015). Selectively Enhancing the Clearance of Pathological Tau Through the Use of Phytochemical Compounds. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30121

Chicago Manual of Style (16th Edition):

Chesser, Adrianne S. “Selectively Enhancing the Clearance of Pathological Tau Through the Use of Phytochemical Compounds.” 2015. Doctoral Dissertation, University of Rochester. Accessed February 19, 2020. http://hdl.handle.net/1802/30121.

MLA Handbook (7th Edition):

Chesser, Adrianne S. “Selectively Enhancing the Clearance of Pathological Tau Through the Use of Phytochemical Compounds.” 2015. Web. 19 Feb 2020.

Vancouver:

Chesser AS. Selectively Enhancing the Clearance of Pathological Tau Through the Use of Phytochemical Compounds. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/1802/30121.

Council of Science Editors:

Chesser AS. Selectively Enhancing the Clearance of Pathological Tau Through the Use of Phytochemical Compounds. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30121


University of Southern California

19. Sharma, Natasha. Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Southern California

 The ability of autophagy to support cancer cells under the conditions of metabolic, chemotherapeutic and endoplasmic reticulum stress (ERS) has led to its emergence as… (more)

Subjects/Keywords: autophagy; mefloquine; cancer; metabolism

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APA (6th Edition):

Sharma, N. (2013). Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3497

Chicago Manual of Style (16th Edition):

Sharma, Natasha. “Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 19, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3497.

MLA Handbook (7th Edition):

Sharma, Natasha. “Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism.” 2013. Web. 19 Feb 2020.

Vancouver:

Sharma N. Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Feb 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3497.

Council of Science Editors:

Sharma N. Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3497


University of Southern California

20. Zhang, Tian. UVRAG mediates Atg9 transport upon autophagy induction.

Degree: MS, Molecular Microbiology and Immunology, 2014, University of Southern California

Autophagy is a cellular process of self‐digestion to maintain homeostasis and avoid cell death. The normal functioning of autophagy is strongly linked to its molecular… (more)

Subjects/Keywords: UVRAG; autophagy; Atg9; Beclin1; autophagosome

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APA (6th Edition):

Zhang, T. (2014). UVRAG mediates Atg9 transport upon autophagy induction. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453471/rec/7788

Chicago Manual of Style (16th Edition):

Zhang, Tian. “UVRAG mediates Atg9 transport upon autophagy induction.” 2014. Masters Thesis, University of Southern California. Accessed February 19, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453471/rec/7788.

MLA Handbook (7th Edition):

Zhang, Tian. “UVRAG mediates Atg9 transport upon autophagy induction.” 2014. Web. 19 Feb 2020.

Vancouver:

Zhang T. UVRAG mediates Atg9 transport upon autophagy induction. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2020 Feb 19]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453471/rec/7788.

Council of Science Editors:

Zhang T. UVRAG mediates Atg9 transport upon autophagy induction. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453471/rec/7788


Boston University

21. Trudeau, Kyle Marvin. The role of mitochondrial dynamics and autophagy in pancreatic beta-cell response to nutrient stress.

Degree: PhD, Molecular and Translational Medicine, 2016, Boston University

 Mitochondrial dynamics includes the processes of fusion, fission, and motility. These processes form interdependent adaptive mechanisms that, together with autophagy, maintain mitochondrial function to meet… (more)

Subjects/Keywords: Biology; Autophagy; Beta-cell; Mitochondria

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APA (6th Edition):

Trudeau, K. M. (2016). The role of mitochondrial dynamics and autophagy in pancreatic beta-cell response to nutrient stress. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16731

Chicago Manual of Style (16th Edition):

Trudeau, Kyle Marvin. “The role of mitochondrial dynamics and autophagy in pancreatic beta-cell response to nutrient stress.” 2016. Doctoral Dissertation, Boston University. Accessed February 19, 2020. http://hdl.handle.net/2144/16731.

MLA Handbook (7th Edition):

Trudeau, Kyle Marvin. “The role of mitochondrial dynamics and autophagy in pancreatic beta-cell response to nutrient stress.” 2016. Web. 19 Feb 2020.

Vancouver:

Trudeau KM. The role of mitochondrial dynamics and autophagy in pancreatic beta-cell response to nutrient stress. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/2144/16731.

Council of Science Editors:

Trudeau KM. The role of mitochondrial dynamics and autophagy in pancreatic beta-cell response to nutrient stress. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/16731


Wright State University

22. Mercer, Carol A. Structural and Signaling Elements Important for the Efficient Degradation of BHMT through Macroautophagy.

Degree: PhD, Biomedical Sciences PhD, 2007, Wright State University

 Healthy cells maintain a dynamic and responsive intracellular environment that is marked by the synthesis and degradation of proteins, complex macromolecules and organelles. Autophagy, literally… (more)

Subjects/Keywords: Autophagy; BHMT; mTOR; S6 kinase

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APA (6th Edition):

Mercer, C. A. (2007). Structural and Signaling Elements Important for the Efficient Degradation of BHMT through Macroautophagy. (Doctoral Dissertation). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1176234559

Chicago Manual of Style (16th Edition):

Mercer, Carol A. “Structural and Signaling Elements Important for the Efficient Degradation of BHMT through Macroautophagy.” 2007. Doctoral Dissertation, Wright State University. Accessed February 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=wright1176234559.

MLA Handbook (7th Edition):

Mercer, Carol A. “Structural and Signaling Elements Important for the Efficient Degradation of BHMT through Macroautophagy.” 2007. Web. 19 Feb 2020.

Vancouver:

Mercer CA. Structural and Signaling Elements Important for the Efficient Degradation of BHMT through Macroautophagy. [Internet] [Doctoral dissertation]. Wright State University; 2007. [cited 2020 Feb 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1176234559.

Council of Science Editors:

Mercer CA. Structural and Signaling Elements Important for the Efficient Degradation of BHMT through Macroautophagy. [Doctoral Dissertation]. Wright State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1176234559


Case Western Reserve University

23. Liu, Elizabeth. The Autophagy Pathway and Toxoplasma gondii Infection.

Degree: PhD, Pathology, 2015, Case Western Reserve University

 Toxoplasma gondii is an intracellular protozoan that resides in a parasitophorous vacuole within infected host cells. This vacuole shields the parasite from lysosomal degradation. Our… (more)

Subjects/Keywords: Immunology; Pathology; Toxoplasma gondii; autophagy

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APA (6th Edition):

Liu, E. (2015). The Autophagy Pathway and Toxoplasma gondii Infection. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1428103561

Chicago Manual of Style (16th Edition):

Liu, Elizabeth. “The Autophagy Pathway and Toxoplasma gondii Infection.” 2015. Doctoral Dissertation, Case Western Reserve University. Accessed February 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1428103561.

MLA Handbook (7th Edition):

Liu, Elizabeth. “The Autophagy Pathway and Toxoplasma gondii Infection.” 2015. Web. 19 Feb 2020.

Vancouver:

Liu E. The Autophagy Pathway and Toxoplasma gondii Infection. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2015. [cited 2020 Feb 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1428103561.

Council of Science Editors:

Liu E. The Autophagy Pathway and Toxoplasma gondii Infection. [Doctoral Dissertation]. Case Western Reserve University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1428103561


NSYSU

24. Lee, Ya-che. Hexane fraction of Pluchea indica (L.) Less. root extract induce autophagic cell death on glioblastoma multiforme U87 cells.

Degree: Master, Biological Sciences, 2016, NSYSU

 Pluchea indica (L.) Less. is a perennial plant known for its versatile uses in traditional oriental medicine. In our previous study, we demonstrate the in… (more)

Subjects/Keywords: Glioblastoma Multiforme; Autophagy; Pluchea indica

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APA (6th Edition):

Lee, Y. (2016). Hexane fraction of Pluchea indica (L.) Less. root extract induce autophagic cell death on glioblastoma multiforme U87 cells. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0508116-175738

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):

Lee, Ya-che. “Hexane fraction of Pluchea indica (L.) Less. root extract induce autophagic cell death on glioblastoma multiforme U87 cells.” 2016. Thesis, NSYSU. Accessed February 19, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0508116-175738.

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

MLA Handbook (7th Edition):

Lee, Ya-che. “Hexane fraction of Pluchea indica (L.) Less. root extract induce autophagic cell death on glioblastoma multiforme U87 cells.” 2016. Web. 19 Feb 2020.

Vancouver:

Lee Y. Hexane fraction of Pluchea indica (L.) Less. root extract induce autophagic cell death on glioblastoma multiforme U87 cells. [Internet] [Thesis]. NSYSU; 2016. [cited 2020 Feb 19]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0508116-175738.

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

Council of Science Editors:

Lee Y. Hexane fraction of Pluchea indica (L.) Less. root extract induce autophagic cell death on glioblastoma multiforme U87 cells. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0508116-175738

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


University of Saskatchewan

25. Bridge, Rylan. INVESTIGATING THE ROLE OF CELLULAR AUTOPHAGY IN HUMAN MONOCYTIC CELL DEATH BY KINOME ANALYSIS.

Degree: 2016, University of Saskatchewan

 Cells of the Monocyte / Macrophage lineage are key players in innate and adaptive immunity. They eliminate pathogens through their phagocytic and antimicrobial properties, secretion… (more)

Subjects/Keywords: autophagy; cell death; kinome analysis

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APA (6th Edition):

Bridge, R. (2016). INVESTIGATING THE ROLE OF CELLULAR AUTOPHAGY IN HUMAN MONOCYTIC CELL DEATH BY KINOME ANALYSIS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7628

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):

Bridge, Rylan. “INVESTIGATING THE ROLE OF CELLULAR AUTOPHAGY IN HUMAN MONOCYTIC CELL DEATH BY KINOME ANALYSIS.” 2016. Thesis, University of Saskatchewan. Accessed February 19, 2020. http://hdl.handle.net/10388/7628.

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

MLA Handbook (7th Edition):

Bridge, Rylan. “INVESTIGATING THE ROLE OF CELLULAR AUTOPHAGY IN HUMAN MONOCYTIC CELL DEATH BY KINOME ANALYSIS.” 2016. Web. 19 Feb 2020.

Vancouver:

Bridge R. INVESTIGATING THE ROLE OF CELLULAR AUTOPHAGY IN HUMAN MONOCYTIC CELL DEATH BY KINOME ANALYSIS. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10388/7628.

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

Council of Science Editors:

Bridge R. INVESTIGATING THE ROLE OF CELLULAR AUTOPHAGY IN HUMAN MONOCYTIC CELL DEATH BY KINOME ANALYSIS. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7628

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


University of Victoria

26. Townsend, Katelin N. Understanding CD8 T cell function under the tumour environment condition hypoxia.

Degree: Dept. of Biochemistry and Microbiology, 2012, University of Victoria

 As CD8 T cells migrate to tumour sites, they experience conditions of low oxygen or hypoxia, in the tumour environment. Hypoxia results due to the… (more)

Subjects/Keywords: Immunology; Cancer; Hypoxia; Autophagy

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APA (6th Edition):

Townsend, K. N. (2012). Understanding CD8 T cell function under the tumour environment condition hypoxia. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/4107

Chicago Manual of Style (16th Edition):

Townsend, Katelin N. “Understanding CD8 T cell function under the tumour environment condition hypoxia.” 2012. Masters Thesis, University of Victoria. Accessed February 19, 2020. http://hdl.handle.net/1828/4107.

MLA Handbook (7th Edition):

Townsend, Katelin N. “Understanding CD8 T cell function under the tumour environment condition hypoxia.” 2012. Web. 19 Feb 2020.

Vancouver:

Townsend KN. Understanding CD8 T cell function under the tumour environment condition hypoxia. [Internet] [Masters thesis]. University of Victoria; 2012. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/1828/4107.

Council of Science Editors:

Townsend KN. Understanding CD8 T cell function under the tumour environment condition hypoxia. [Masters Thesis]. University of Victoria; 2012. Available from: http://hdl.handle.net/1828/4107

27. 유, 경남. The role of autophagy in allergic inflammation: a new target for severe asthma.

Degree: 2015, Ajou University

I.INTRODUCTION 1 II.MATERIALS AND METHODS 4 1. Mice 4 2. EthicsStatement 4 3. Sensitization and challenge 4 4. Treatment protocols 5 5. Airway resistance measurements… (more)

Subjects/Keywords: Allergicasthma; Autophagy; Eosinophil; Interleukin 5

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APA (6th Edition):

유, . (2015). The role of autophagy in allergic inflammation: a new target for severe asthma. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/11902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000020525

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):

유, 경남. “The role of autophagy in allergic inflammation: a new target for severe asthma.” 2015. Thesis, Ajou University. Accessed February 19, 2020. http://repository.ajou.ac.kr/handle/201003/11902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000020525.

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

MLA Handbook (7th Edition):

유, 경남. “The role of autophagy in allergic inflammation: a new target for severe asthma.” 2015. Web. 19 Feb 2020.

Vancouver:

유 . The role of autophagy in allergic inflammation: a new target for severe asthma. [Internet] [Thesis]. Ajou University; 2015. [cited 2020 Feb 19]. Available from: http://repository.ajou.ac.kr/handle/201003/11902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000020525.

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

Council of Science Editors:

유 . The role of autophagy in allergic inflammation: a new target for severe asthma. [Thesis]. Ajou University; 2015. Available from: http://repository.ajou.ac.kr/handle/201003/11902 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000020525

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


Virginia Tech

28. Su, Shengchen. Cellular Events During Coccidial Infection in Chickens.

Degree: PhD, Animal and Poultry Sciences, 2016, Virginia Tech

 Avian coccidiosis is caused by the intestinal protozoa Eimeria. The parasite's site of infection in the intestine is site specific. Eimeria acervulina mainly affects the… (more)

Subjects/Keywords: Eimeria; transporter; HDPs; apoptosis; autophagy

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

APA (6th Edition):

Su, S. (2016). Cellular Events During Coccidial Infection in Chickens. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/82505

Chicago Manual of Style (16th Edition):

Su, Shengchen. “Cellular Events During Coccidial Infection in Chickens.” 2016. Doctoral Dissertation, Virginia Tech. Accessed February 19, 2020. http://hdl.handle.net/10919/82505.

MLA Handbook (7th Edition):

Su, Shengchen. “Cellular Events During Coccidial Infection in Chickens.” 2016. Web. 19 Feb 2020.

Vancouver:

Su S. Cellular Events During Coccidial Infection in Chickens. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10919/82505.

Council of Science Editors:

Su S. Cellular Events During Coccidial Infection in Chickens. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/82505


Deakin University

29. Al Shamaileh, Hadi. Aptamer-mediated siRNA delivery to target colon cancer stem cells.

Degree: School of Medicine, 2016, Deakin University

 Cancer stem cells are often referred to as the root of cancer as they drive tumour growth and are resistant to traditional anti-cancer therapies. By… (more)

Subjects/Keywords: Cancer; Stem cell research; Autophagy

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

APA (6th Edition):

Al Shamaileh, H. (2016). Aptamer-mediated siRNA delivery to target colon cancer stem cells. (Thesis). Deakin University. Retrieved from http://hdl.handle.net/10536/DRO/DU:30088970

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):

Al Shamaileh, Hadi. “Aptamer-mediated siRNA delivery to target colon cancer stem cells.” 2016. Thesis, Deakin University. Accessed February 19, 2020. http://hdl.handle.net/10536/DRO/DU:30088970.

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

MLA Handbook (7th Edition):

Al Shamaileh, Hadi. “Aptamer-mediated siRNA delivery to target colon cancer stem cells.” 2016. Web. 19 Feb 2020.

Vancouver:

Al Shamaileh H. Aptamer-mediated siRNA delivery to target colon cancer stem cells. [Internet] [Thesis]. Deakin University; 2016. [cited 2020 Feb 19]. Available from: http://hdl.handle.net/10536/DRO/DU:30088970.

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

Council of Science Editors:

Al Shamaileh H. Aptamer-mediated siRNA delivery to target colon cancer stem cells. [Thesis]. Deakin University; 2016. Available from: http://hdl.handle.net/10536/DRO/DU:30088970

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


University of Cambridge

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

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 February 19, 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. 19 Feb 2020.

Vancouver:

Yu Q. Identification of regulators in autophagosome formation using image-based siRNA screening. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Feb 19]. 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

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