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You searched for subject:(Cellular metabolism). Showing records 1 – 30 of 185 total matches.

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Vanderbilt University

1. Hardeman, Keisha Nicole. Cellular Metabolism Contributes To Therapeutic Responses in BRAF-Mutated Melanomas.

Degree: PhD, Cancer Biology, 2017, Vanderbilt University

 Melanoma is the deadliest form of skin cancer, and virtually all patients progress on targeted therapies. Dysregulated metabolism has been shown to affect therapy response,… (more)

Subjects/Keywords: metabolic reprogramming; melanoma; cellular metabolism; glycolysis

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APA (6th Edition):

Hardeman, K. N. (2017). Cellular Metabolism Contributes To Therapeutic Responses in BRAF-Mutated Melanomas. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12123

Chicago Manual of Style (16th Edition):

Hardeman, Keisha Nicole. “Cellular Metabolism Contributes To Therapeutic Responses in BRAF-Mutated Melanomas.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed September 22, 2020. http://hdl.handle.net/1803/12123.

MLA Handbook (7th Edition):

Hardeman, Keisha Nicole. “Cellular Metabolism Contributes To Therapeutic Responses in BRAF-Mutated Melanomas.” 2017. Web. 22 Sep 2020.

Vancouver:

Hardeman KN. Cellular Metabolism Contributes To Therapeutic Responses in BRAF-Mutated Melanomas. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1803/12123.

Council of Science Editors:

Hardeman KN. Cellular Metabolism Contributes To Therapeutic Responses in BRAF-Mutated Melanomas. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/12123


Harvard University

2. Stanley, Illana Allake. Metabolic Heterogeneity in Molecular Subsets of Diffuse Large B-cell Lymphoma.

Degree: PhD, Biology: Medical Sciences, Division of, 2014, Harvard University

 Cells adapt their metabolism to satisfy changing bioenergetic and biosynthetic needs. Investigation of metabolic reprogramming in cancer has provided insight into the metabolic control of… (more)

Subjects/Keywords: Cellular biology; cancer; DLBCL; lymphoma; metabolism; mitochondria

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APA (6th Edition):

Stanley, I. A. (2014). Metabolic Heterogeneity in Molecular Subsets of Diffuse Large B-cell Lymphoma. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:13069713

Chicago Manual of Style (16th Edition):

Stanley, Illana Allake. “Metabolic Heterogeneity in Molecular Subsets of Diffuse Large B-cell Lymphoma.” 2014. Doctoral Dissertation, Harvard University. Accessed September 22, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13069713.

MLA Handbook (7th Edition):

Stanley, Illana Allake. “Metabolic Heterogeneity in Molecular Subsets of Diffuse Large B-cell Lymphoma.” 2014. Web. 22 Sep 2020.

Vancouver:

Stanley IA. Metabolic Heterogeneity in Molecular Subsets of Diffuse Large B-cell Lymphoma. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Sep 22]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13069713.

Council of Science Editors:

Stanley IA. Metabolic Heterogeneity in Molecular Subsets of Diffuse Large B-cell Lymphoma. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13069713


University of New South Wales

3. Chang, Teddy. Synthesis of amphilic block copolymers for study of cellular interaction and uptake.

Degree: Centre for Advanced Macromolecular Design, 2012, University of New South Wales

 Therapeutics once administered into the human body begins to degrade almost immediately. This is a result of the body metabolizing the drug once it enters… (more)

Subjects/Keywords: amphilic block copolymers; therapeutics; metabolism; polymers; cellular uptake; cellular interaction

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APA (6th Edition):

Chang, T. (2012). Synthesis of amphilic block copolymers for study of cellular interaction and uptake. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/52048 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10718/SOURCE01?view=true

Chicago Manual of Style (16th Edition):

Chang, Teddy. “Synthesis of amphilic block copolymers for study of cellular interaction and uptake.” 2012. Masters Thesis, University of New South Wales. Accessed September 22, 2020. http://handle.unsw.edu.au/1959.4/52048 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10718/SOURCE01?view=true.

MLA Handbook (7th Edition):

Chang, Teddy. “Synthesis of amphilic block copolymers for study of cellular interaction and uptake.” 2012. Web. 22 Sep 2020.

Vancouver:

Chang T. Synthesis of amphilic block copolymers for study of cellular interaction and uptake. [Internet] [Masters thesis]. University of New South Wales; 2012. [cited 2020 Sep 22]. Available from: http://handle.unsw.edu.au/1959.4/52048 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10718/SOURCE01?view=true.

Council of Science Editors:

Chang T. Synthesis of amphilic block copolymers for study of cellular interaction and uptake. [Masters Thesis]. University of New South Wales; 2012. Available from: http://handle.unsw.edu.au/1959.4/52048 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10718/SOURCE01?view=true


University of California – San Francisco

4. Goldsmith, Juliet Eve. Translation regulation by autophagy and nutrient stress.

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

 Protein translation is necessary for cell function, but it is an incredibly energy demanding process, and is therefore tightly regulated by the metabolic state of… (more)

Subjects/Keywords: Cellular biology; Molecular biology; Autophagy; BRCA2; Cellular metabolism; Protein translation; RNA binding proteins

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APA (6th Edition):

Goldsmith, J. E. (2018). Translation regulation by autophagy and nutrient stress. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/59h0f8gw

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):

Goldsmith, Juliet Eve. “Translation regulation by autophagy and nutrient stress.” 2018. Thesis, University of California – San Francisco. Accessed September 22, 2020. http://www.escholarship.org/uc/item/59h0f8gw.

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

MLA Handbook (7th Edition):

Goldsmith, Juliet Eve. “Translation regulation by autophagy and nutrient stress.” 2018. Web. 22 Sep 2020.

Vancouver:

Goldsmith JE. Translation regulation by autophagy and nutrient stress. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/59h0f8gw.

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

Council of Science Editors:

Goldsmith JE. Translation regulation by autophagy and nutrient stress. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/59h0f8gw

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


Duke University

5. Yuan, Lifeng. Identification of Molecular Determinants of Cellular Senescence in Cancer and Aging .

Degree: 2018, Duke University

Cellular senescence is a fundamental cell fate playing significant and complex roles during tumorigenesis and natural aging process. However, the molecular determinants distinguishing senescence… (more)

Subjects/Keywords: Molecular biology; Cellular biology; Biochemistry; Aging; Cell Death; Cellular Senescence; Healthy Longevity; Metabolism; Mitochondria

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APA (6th Edition):

Yuan, L. (2018). Identification of Molecular Determinants of Cellular Senescence in Cancer and Aging . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/17470

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):

Yuan, Lifeng. “Identification of Molecular Determinants of Cellular Senescence in Cancer and Aging .” 2018. Thesis, Duke University. Accessed September 22, 2020. http://hdl.handle.net/10161/17470.

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

MLA Handbook (7th Edition):

Yuan, Lifeng. “Identification of Molecular Determinants of Cellular Senescence in Cancer and Aging .” 2018. Web. 22 Sep 2020.

Vancouver:

Yuan L. Identification of Molecular Determinants of Cellular Senescence in Cancer and Aging . [Internet] [Thesis]. Duke University; 2018. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/10161/17470.

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

Council of Science Editors:

Yuan L. Identification of Molecular Determinants of Cellular Senescence in Cancer and Aging . [Thesis]. Duke University; 2018. Available from: http://hdl.handle.net/10161/17470

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


UCLA

6. Flores, Aimee Alyssa. Investigating the Role of Metabolism in Tissue Homeostasis and Tumor Initiation by Hair Follicle Stem Cells.

Degree: Molecular Biology, 2018, UCLA

 For an increasing number of cancers, the cell of origin has been demonstrated to be theresident adult stem cell. One such cancer is squamous cell… (more)

Subjects/Keywords: Molecular biology; Cellular biology; Developmental biology; Adult Stem Cells; Cancer Metabolism; Cellular Metabolism; Hair Follicle Stem Cells

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APA (6th Edition):

Flores, A. A. (2018). Investigating the Role of Metabolism in Tissue Homeostasis and Tumor Initiation by Hair Follicle Stem Cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/4936t5nd

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):

Flores, Aimee Alyssa. “Investigating the Role of Metabolism in Tissue Homeostasis and Tumor Initiation by Hair Follicle Stem Cells.” 2018. Thesis, UCLA. Accessed September 22, 2020. http://www.escholarship.org/uc/item/4936t5nd.

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

MLA Handbook (7th Edition):

Flores, Aimee Alyssa. “Investigating the Role of Metabolism in Tissue Homeostasis and Tumor Initiation by Hair Follicle Stem Cells.” 2018. Web. 22 Sep 2020.

Vancouver:

Flores AA. Investigating the Role of Metabolism in Tissue Homeostasis and Tumor Initiation by Hair Follicle Stem Cells. [Internet] [Thesis]. UCLA; 2018. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/4936t5nd.

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

Council of Science Editors:

Flores AA. Investigating the Role of Metabolism in Tissue Homeostasis and Tumor Initiation by Hair Follicle Stem Cells. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/4936t5nd

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

7. Neumann, Chase K. A. Phosphatidylinositol Remodeling through Membrane Bound O-acyl Transferase Domain-7 (MBOAT7) Promotes the Progression of Clear Cell Renal Cell Carcinoma (ccRCC).

Degree: PhD, Molecular Medicine, 2020, Case Western Reserve University School of Graduate Studies

 In the metabolism of cancer, phosphatidylinositols (PI) sit at the apex of signaling decisions and structure. PI phospholipids like other phospholipids can be synthesized via… (more)

Subjects/Keywords: Cellular Biology; Biochemistry; Oncology; Molecular Biology; Cancer metabolism; Lipid metabolism; MBOAT7; Lands Cycle

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APA (6th Edition):

Neumann, C. K. A. (2020). Phosphatidylinositol Remodeling through Membrane Bound O-acyl Transferase Domain-7 (MBOAT7) Promotes the Progression of Clear Cell Renal Cell Carcinoma (ccRCC). (Doctoral Dissertation). Case Western Reserve University School of Graduate Studies. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1586250046745924

Chicago Manual of Style (16th Edition):

Neumann, Chase K A. “Phosphatidylinositol Remodeling through Membrane Bound O-acyl Transferase Domain-7 (MBOAT7) Promotes the Progression of Clear Cell Renal Cell Carcinoma (ccRCC).” 2020. Doctoral Dissertation, Case Western Reserve University School of Graduate Studies. Accessed September 22, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1586250046745924.

MLA Handbook (7th Edition):

Neumann, Chase K A. “Phosphatidylinositol Remodeling through Membrane Bound O-acyl Transferase Domain-7 (MBOAT7) Promotes the Progression of Clear Cell Renal Cell Carcinoma (ccRCC).” 2020. Web. 22 Sep 2020.

Vancouver:

Neumann CKA. Phosphatidylinositol Remodeling through Membrane Bound O-acyl Transferase Domain-7 (MBOAT7) Promotes the Progression of Clear Cell Renal Cell Carcinoma (ccRCC). [Internet] [Doctoral dissertation]. Case Western Reserve University School of Graduate Studies; 2020. [cited 2020 Sep 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1586250046745924.

Council of Science Editors:

Neumann CKA. Phosphatidylinositol Remodeling through Membrane Bound O-acyl Transferase Domain-7 (MBOAT7) Promotes the Progression of Clear Cell Renal Cell Carcinoma (ccRCC). [Doctoral Dissertation]. Case Western Reserve University School of Graduate Studies; 2020. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1586250046745924


University of California – Irvine

8. Ramirez, Manuel U. Starving cancer: the molecular mechanisms of nutrient transporter loss induced by anti-neoplastic sphingolipids.

Degree: Biological Sciences, 2017, University of California – Irvine

 Sphingolipids are found in all kingdoms of life. In mammals, sphingolipids regulate multiple cellular processes. Ceramide is a sphingolipid of interest to cancer biologists due… (more)

Subjects/Keywords: Biology; Molecular biology; Cellular biology; Arf6; Cancer; Metabolism; Sphingolipid

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APA (6th Edition):

Ramirez, M. U. (2017). Starving cancer: the molecular mechanisms of nutrient transporter loss induced by anti-neoplastic sphingolipids. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/2kp8054c

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):

Ramirez, Manuel U. “Starving cancer: the molecular mechanisms of nutrient transporter loss induced by anti-neoplastic sphingolipids.” 2017. Thesis, University of California – Irvine. Accessed September 22, 2020. http://www.escholarship.org/uc/item/2kp8054c.

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

MLA Handbook (7th Edition):

Ramirez, Manuel U. “Starving cancer: the molecular mechanisms of nutrient transporter loss induced by anti-neoplastic sphingolipids.” 2017. Web. 22 Sep 2020.

Vancouver:

Ramirez MU. Starving cancer: the molecular mechanisms of nutrient transporter loss induced by anti-neoplastic sphingolipids. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/2kp8054c.

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

Council of Science Editors:

Ramirez MU. Starving cancer: the molecular mechanisms of nutrient transporter loss induced by anti-neoplastic sphingolipids. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/2kp8054c

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


University of California – San Diego

9. Parker, Seth Jameson. Tracing Compartmentalized Metabolism in Mutant IDH Cancer Cells.

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

Cellular metabolism comprises of a network of reactions responsible for converting nutrients into energy and building blocks necessary for cells to carry out specific functions… (more)

Subjects/Keywords: Biomedical engineering; Biochemistry; Cellular biology; Cancer; Metabolism; Mitochondria; NADPH; TCA Cycle

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APA (6th Edition):

Parker, S. J. (2016). Tracing Compartmentalized Metabolism in Mutant IDH Cancer Cells. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9w39c4hn

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):

Parker, Seth Jameson. “Tracing Compartmentalized Metabolism in Mutant IDH Cancer Cells.” 2016. Thesis, University of California – San Diego. Accessed September 22, 2020. http://www.escholarship.org/uc/item/9w39c4hn.

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

MLA Handbook (7th Edition):

Parker, Seth Jameson. “Tracing Compartmentalized Metabolism in Mutant IDH Cancer Cells.” 2016. Web. 22 Sep 2020.

Vancouver:

Parker SJ. Tracing Compartmentalized Metabolism in Mutant IDH Cancer Cells. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/9w39c4hn.

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

Council of Science Editors:

Parker SJ. Tracing Compartmentalized Metabolism in Mutant IDH Cancer Cells. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/9w39c4hn

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


University of California – Berkeley

10. Benjamin, Daniel Isaac. Mapping Dysregulated Metabolic Pathways in Cancer Using Functional Metabolomic Platforms.

Degree: Molecular & Biochemical Nutrition, 2015, University of California – Berkeley

 Cancer cells possess fundamentally altered metabolic pathways that provide a foundation to support tumorigenicity and malignancy. Our understanding of the biochemical underpinnings of cancer has… (more)

Subjects/Keywords: Cellular biology; Biochemistry; Molecular biology; Cancer; Metabolism; Metabolomics

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APA (6th Edition):

Benjamin, D. I. (2015). Mapping Dysregulated Metabolic Pathways in Cancer Using Functional Metabolomic Platforms. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4vr6d02p

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):

Benjamin, Daniel Isaac. “Mapping Dysregulated Metabolic Pathways in Cancer Using Functional Metabolomic Platforms.” 2015. Thesis, University of California – Berkeley. Accessed September 22, 2020. http://www.escholarship.org/uc/item/4vr6d02p.

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

MLA Handbook (7th Edition):

Benjamin, Daniel Isaac. “Mapping Dysregulated Metabolic Pathways in Cancer Using Functional Metabolomic Platforms.” 2015. Web. 22 Sep 2020.

Vancouver:

Benjamin DI. Mapping Dysregulated Metabolic Pathways in Cancer Using Functional Metabolomic Platforms. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/4vr6d02p.

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

Council of Science Editors:

Benjamin DI. Mapping Dysregulated Metabolic Pathways in Cancer Using Functional Metabolomic Platforms. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/4vr6d02p

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


University of California – Berkeley

11. Hunerdosse, Devon. Using Chemoproteomic and Metabolomic Platforms to Identify Nodal Metabolic Pathways Important to Inflammation.

Degree: Endocrinology, 2015, University of California – Berkeley

 There are an increasing number of human pathologies that have been associated with altered metabolism, including obesity, diabetes, cancer, atherosclerosis, and neurodegenerative diseases. Most attention… (more)

Subjects/Keywords: Biology; Cellular biology; Molecular biology; Inflammation; Lipid metabolism; Metabolomics; Proteomics

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APA (6th Edition):

Hunerdosse, D. (2015). Using Chemoproteomic and Metabolomic Platforms to Identify Nodal Metabolic Pathways Important to Inflammation. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/53r571cj

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):

Hunerdosse, Devon. “Using Chemoproteomic and Metabolomic Platforms to Identify Nodal Metabolic Pathways Important to Inflammation.” 2015. Thesis, University of California – Berkeley. Accessed September 22, 2020. http://www.escholarship.org/uc/item/53r571cj.

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

MLA Handbook (7th Edition):

Hunerdosse, Devon. “Using Chemoproteomic and Metabolomic Platforms to Identify Nodal Metabolic Pathways Important to Inflammation.” 2015. Web. 22 Sep 2020.

Vancouver:

Hunerdosse D. Using Chemoproteomic and Metabolomic Platforms to Identify Nodal Metabolic Pathways Important to Inflammation. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/53r571cj.

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

Council of Science Editors:

Hunerdosse D. Using Chemoproteomic and Metabolomic Platforms to Identify Nodal Metabolic Pathways Important to Inflammation. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/53r571cj

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


University of California – Irvine

12. Araujo, Lindsey Renee. The Warburg effect controls cell growth and differentiation by altering N-glycosylation.

Degree: Biomedical Sciences, 2015, University of California – Irvine

 Rapidly proliferating cells such as T cells undergo the Warburg effect [1-3], a long-standing and poorly understood phenomenon that increases glucose uptake yet paradoxically reduces… (more)

Subjects/Keywords: Immunology; Cellular biology; Differentiation; Glycolysis; Hexosamine; Metabolism; N-glycosylation; Warburg

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APA (6th Edition):

Araujo, L. R. (2015). The Warburg effect controls cell growth and differentiation by altering N-glycosylation. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/45z7q3m9

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):

Araujo, Lindsey Renee. “The Warburg effect controls cell growth and differentiation by altering N-glycosylation.” 2015. Thesis, University of California – Irvine. Accessed September 22, 2020. http://www.escholarship.org/uc/item/45z7q3m9.

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

MLA Handbook (7th Edition):

Araujo, Lindsey Renee. “The Warburg effect controls cell growth and differentiation by altering N-glycosylation.” 2015. Web. 22 Sep 2020.

Vancouver:

Araujo LR. The Warburg effect controls cell growth and differentiation by altering N-glycosylation. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/45z7q3m9.

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

Council of Science Editors:

Araujo LR. The Warburg effect controls cell growth and differentiation by altering N-glycosylation. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/45z7q3m9

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


University of Michigan

13. Kucinski, Jan. Functional Characterization of Selected Chloroplast RNA-Binding Proteins from Arabidopsis thaliana.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2020, University of Michigan

 Plastids are indispensable, plant-specific organelles of prokaryotic origin. They serve a plethora of biological functions crucial for plant metabolism. Plastids contain their own genomes, which… (more)

Subjects/Keywords: Plastid RNA metabolism; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Kucinski, J. (2020). Functional Characterization of Selected Chloroplast RNA-Binding Proteins from Arabidopsis thaliana. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/155223

Chicago Manual of Style (16th Edition):

Kucinski, Jan. “Functional Characterization of Selected Chloroplast RNA-Binding Proteins from Arabidopsis thaliana.” 2020. Doctoral Dissertation, University of Michigan. Accessed September 22, 2020. http://hdl.handle.net/2027.42/155223.

MLA Handbook (7th Edition):

Kucinski, Jan. “Functional Characterization of Selected Chloroplast RNA-Binding Proteins from Arabidopsis thaliana.” 2020. Web. 22 Sep 2020.

Vancouver:

Kucinski J. Functional Characterization of Selected Chloroplast RNA-Binding Proteins from Arabidopsis thaliana. [Internet] [Doctoral dissertation]. University of Michigan; 2020. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/2027.42/155223.

Council of Science Editors:

Kucinski J. Functional Characterization of Selected Chloroplast RNA-Binding Proteins from Arabidopsis thaliana. [Doctoral Dissertation]. University of Michigan; 2020. Available from: http://hdl.handle.net/2027.42/155223


Vanderbilt University

14. Walsh, Alexandra Jule. Optical imaging of metabolism in HER2 overexpressing cells.

Degree: MS, Biomedical Engineering, 2012, Vanderbilt University

 The optical redox ratio (fluorescence intensity of NADH divided by that of FAD), was acquired for a panel of breast cancer cell lines to investigate… (more)

Subjects/Keywords: fluorescence; NADH; FAD; optical redox ratio; breast cancer; cellular metabolism; resistance

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APA (6th Edition):

Walsh, A. J. (2012). Optical imaging of metabolism in HER2 overexpressing cells. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11415

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):

Walsh, Alexandra Jule. “Optical imaging of metabolism in HER2 overexpressing cells.” 2012. Thesis, Vanderbilt University. Accessed September 22, 2020. http://hdl.handle.net/1803/11415.

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

MLA Handbook (7th Edition):

Walsh, Alexandra Jule. “Optical imaging of metabolism in HER2 overexpressing cells.” 2012. Web. 22 Sep 2020.

Vancouver:

Walsh AJ. Optical imaging of metabolism in HER2 overexpressing cells. [Internet] [Thesis]. Vanderbilt University; 2012. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1803/11415.

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

Council of Science Editors:

Walsh AJ. Optical imaging of metabolism in HER2 overexpressing cells. [Thesis]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/11415

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


Vanderbilt University

15. Gil, Daniel Ari. Assessing Tracheal Health Using Optical Metabolic Imaging and Optical Coherence Tomography.

Degree: MS, Biomedical Engineering, 2016, Vanderbilt University

 New therapies are needed to improve the mortality and morbidity of respiratory diseases, but few drug candidates for respiratory diseases are developed and only 3%… (more)

Subjects/Keywords: optical coherence tomography; trachea; cilia; autofluorescence; cellular metabolism

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APA (6th Edition):

Gil, D. A. (2016). Assessing Tracheal Health Using Optical Metabolic Imaging and Optical Coherence Tomography. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14704

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):

Gil, Daniel Ari. “Assessing Tracheal Health Using Optical Metabolic Imaging and Optical Coherence Tomography.” 2016. Thesis, Vanderbilt University. Accessed September 22, 2020. http://hdl.handle.net/1803/14704.

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

MLA Handbook (7th Edition):

Gil, Daniel Ari. “Assessing Tracheal Health Using Optical Metabolic Imaging and Optical Coherence Tomography.” 2016. Web. 22 Sep 2020.

Vancouver:

Gil DA. Assessing Tracheal Health Using Optical Metabolic Imaging and Optical Coherence Tomography. [Internet] [Thesis]. Vanderbilt University; 2016. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1803/14704.

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

Council of Science Editors:

Gil DA. Assessing Tracheal Health Using Optical Metabolic Imaging and Optical Coherence Tomography. [Thesis]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/14704

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


Vanderbilt University

16. Walsh, Alexandra Jule. Development of Optical Imaging of Metabolism for Monitoring and Predicting Drug Efficacy.

Degree: PhD, Biomedical Engineering, 2015, Vanderbilt University

 A clinical need exists for improved methods to identify cancer patients with tumors prone to drug resistance, and prescribe effective alternative therapies. Cellular metabolism is… (more)

Subjects/Keywords: NADH; fluorescence lifetime imaging; cellular metabolism; FAD; breast cancer; organoids

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APA (6th Edition):

Walsh, A. J. (2015). Development of Optical Imaging of Metabolism for Monitoring and Predicting Drug Efficacy. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10712

Chicago Manual of Style (16th Edition):

Walsh, Alexandra Jule. “Development of Optical Imaging of Metabolism for Monitoring and Predicting Drug Efficacy.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed September 22, 2020. http://hdl.handle.net/1803/10712.

MLA Handbook (7th Edition):

Walsh, Alexandra Jule. “Development of Optical Imaging of Metabolism for Monitoring and Predicting Drug Efficacy.” 2015. Web. 22 Sep 2020.

Vancouver:

Walsh AJ. Development of Optical Imaging of Metabolism for Monitoring and Predicting Drug Efficacy. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1803/10712.

Council of Science Editors:

Walsh AJ. Development of Optical Imaging of Metabolism for Monitoring and Predicting Drug Efficacy. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/10712


University of Hyderabad

17. Rao,verkata rama K. Cellular and subcellular transport and metabolism of branched chain amino acids in young Adult and aged bat brain; _.

Degree: Animal sciences, 1995, University of Hyderabad

None

_

Advisors/Committee Members: Murthy, R K.

Subjects/Keywords: Cellular; Subcellular; Transport; Metabolism; Branchedchain

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APA (6th Edition):

K, R. r. (1995). Cellular and subcellular transport and metabolism of branched chain amino acids in young Adult and aged bat brain; _. (Thesis). University of Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/25692

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):

K, Rao,verkata rama. “Cellular and subcellular transport and metabolism of branched chain amino acids in young Adult and aged bat brain; _.” 1995. Thesis, University of Hyderabad. Accessed September 22, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/25692.

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

MLA Handbook (7th Edition):

K, Rao,verkata rama. “Cellular and subcellular transport and metabolism of branched chain amino acids in young Adult and aged bat brain; _.” 1995. Web. 22 Sep 2020.

Vancouver:

K Rr. Cellular and subcellular transport and metabolism of branched chain amino acids in young Adult and aged bat brain; _. [Internet] [Thesis]. University of Hyderabad; 1995. [cited 2020 Sep 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25692.

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

Council of Science Editors:

K Rr. Cellular and subcellular transport and metabolism of branched chain amino acids in young Adult and aged bat brain; _. [Thesis]. University of Hyderabad; 1995. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/25692

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


University of Toronto

18. Chan, Olivia. The Role of CCL5/RANTES in Regulating Cellular Metabolism in Activated T cells.

Degree: 2011, University of Toronto

Recruitment of effector T cells to sites of infection is essential for an effective adaptive immune response. The inflammatory chemokine CCL5/RANTES activates its cognate receptor,… (more)

Subjects/Keywords: Chemokines; T Lymphocytes; Cellular Metabolism; Signal Transduction; 0982

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

APA (6th Edition):

Chan, O. (2011). The Role of CCL5/RANTES in Regulating Cellular Metabolism in Activated T cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30539

Chicago Manual of Style (16th Edition):

Chan, Olivia. “The Role of CCL5/RANTES in Regulating Cellular Metabolism in Activated T cells.” 2011. Masters Thesis, University of Toronto. Accessed September 22, 2020. http://hdl.handle.net/1807/30539.

MLA Handbook (7th Edition):

Chan, Olivia. “The Role of CCL5/RANTES in Regulating Cellular Metabolism in Activated T cells.” 2011. Web. 22 Sep 2020.

Vancouver:

Chan O. The Role of CCL5/RANTES in Regulating Cellular Metabolism in Activated T cells. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1807/30539.

Council of Science Editors:

Chan O. The Role of CCL5/RANTES in Regulating Cellular Metabolism in Activated T cells. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30539


University of Cincinnati

19. Udobi, Kenea C. The Critical Period for Creatine Transporter Deficiency.

Degree: PhD, Medicine: Neuroscience/Medical Science Scholars Interdisciplinary, 2018, University of Cincinnati

 The discovery of the creatine (Cr)-phosphocreatine (PCr) system has had profound impact on the understanding of cellular bioenergetics, physiology and human pathology. Cr is essential… (more)

Subjects/Keywords: Neurology; creatine; cellular metabolism; mitochondria; intellectual disability; creatine transporter

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APA (6th Edition):

Udobi, K. C. (2018). The Critical Period for Creatine Transporter Deficiency. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1543838614741075

Chicago Manual of Style (16th Edition):

Udobi, Kenea C. “The Critical Period for Creatine Transporter Deficiency.” 2018. Doctoral Dissertation, University of Cincinnati. Accessed September 22, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1543838614741075.

MLA Handbook (7th Edition):

Udobi, Kenea C. “The Critical Period for Creatine Transporter Deficiency.” 2018. Web. 22 Sep 2020.

Vancouver:

Udobi KC. The Critical Period for Creatine Transporter Deficiency. [Internet] [Doctoral dissertation]. University of Cincinnati; 2018. [cited 2020 Sep 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1543838614741075.

Council of Science Editors:

Udobi KC. The Critical Period for Creatine Transporter Deficiency. [Doctoral Dissertation]. University of Cincinnati; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1543838614741075


University of California – San Francisco

20. Jeng, Mark Yungjie. Elucidating Molecular Changes in CD8+ T cells During Aging.

Degree: Biomedical Sciences, 2016, University of California – San Francisco

 One of the consequences of human aging is an overall decline in immune function. A hallmark of this aging process, termed immunosenescence, is the downregulation… (more)

Subjects/Keywords: Immunology; Aging; Cellular biology; Aging; CD8 T cell; FoxO1; Metabolism; SIRT1

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APA (6th Edition):

Jeng, M. Y. (2016). Elucidating Molecular Changes in CD8+ T cells During Aging. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9m81j4k6

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):

Jeng, Mark Yungjie. “Elucidating Molecular Changes in CD8+ T cells During Aging.” 2016. Thesis, University of California – San Francisco. Accessed September 22, 2020. http://www.escholarship.org/uc/item/9m81j4k6.

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

MLA Handbook (7th Edition):

Jeng, Mark Yungjie. “Elucidating Molecular Changes in CD8+ T cells During Aging.” 2016. Web. 22 Sep 2020.

Vancouver:

Jeng MY. Elucidating Molecular Changes in CD8+ T cells During Aging. [Internet] [Thesis]. University of California – San Francisco; 2016. [cited 2020 Sep 22]. Available from: http://www.escholarship.org/uc/item/9m81j4k6.

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

Council of Science Editors:

Jeng MY. Elucidating Molecular Changes in CD8+ T cells During Aging. [Thesis]. University of California – San Francisco; 2016. Available from: http://www.escholarship.org/uc/item/9m81j4k6

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


University of Bath

21. White, Ian R. Thymic nuclear ADPRT.

Degree: PhD, 1988, University of Bath

Subjects/Keywords: 572; Enzymes in cellular metabolism

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

APA (6th Edition):

White, I. R. (1988). Thymic nuclear ADPRT. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/thymic-nuclear-adprt(6f60e637-d225-4ddb-a8f0-e67bc436a4f7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383328

Chicago Manual of Style (16th Edition):

White, Ian R. “Thymic nuclear ADPRT.” 1988. Doctoral Dissertation, University of Bath. Accessed September 22, 2020. https://researchportal.bath.ac.uk/en/studentthesis/thymic-nuclear-adprt(6f60e637-d225-4ddb-a8f0-e67bc436a4f7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383328.

MLA Handbook (7th Edition):

White, Ian R. “Thymic nuclear ADPRT.” 1988. Web. 22 Sep 2020.

Vancouver:

White IR. Thymic nuclear ADPRT. [Internet] [Doctoral dissertation]. University of Bath; 1988. [cited 2020 Sep 22]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/thymic-nuclear-adprt(6f60e637-d225-4ddb-a8f0-e67bc436a4f7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383328.

Council of Science Editors:

White IR. Thymic nuclear ADPRT. [Doctoral Dissertation]. University of Bath; 1988. Available from: https://researchportal.bath.ac.uk/en/studentthesis/thymic-nuclear-adprt(6f60e637-d225-4ddb-a8f0-e67bc436a4f7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383328


University of Sydney

22. Cheng, Delfine. Structure-function properties of the gastrodigestive and hepatic systems of zebrafish (Danio rerio) .

Degree: 2018, University of Sydney

 While they lack mammal-specific organs, zebrafish provide a high degree of resemblance in their genetic profile, molecular mechanisms and organ physiology to humans and have… (more)

Subjects/Keywords: cellular transport; correlative microscopy; metabolism; multi-modal scene understanding; ultrastructure

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APA (6th Edition):

Cheng, D. (2018). Structure-function properties of the gastrodigestive and hepatic systems of zebrafish (Danio rerio) . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/19797

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):

Cheng, Delfine. “Structure-function properties of the gastrodigestive and hepatic systems of zebrafish (Danio rerio) .” 2018. Thesis, University of Sydney. Accessed September 22, 2020. http://hdl.handle.net/2123/19797.

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

MLA Handbook (7th Edition):

Cheng, Delfine. “Structure-function properties of the gastrodigestive and hepatic systems of zebrafish (Danio rerio) .” 2018. Web. 22 Sep 2020.

Vancouver:

Cheng D. Structure-function properties of the gastrodigestive and hepatic systems of zebrafish (Danio rerio) . [Internet] [Thesis]. University of Sydney; 2018. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/2123/19797.

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

Council of Science Editors:

Cheng D. Structure-function properties of the gastrodigestive and hepatic systems of zebrafish (Danio rerio) . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/19797

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


Florida Atlantic University

23. Liu, Min. RNA oxidative damage and ribosomal RNA surveillance under oxidative stress.

Degree: PhD, 2012, Florida Atlantic University

Summary: We have studies oxidative damage of RNA, a major type of cellular macromolecules. RNA is a primary target of reactive oxygen species (ROS). Under… (more)

Subjects/Keywords: RNA – Metabolism; Cellular signal transduction; Genetic translation; Molecular biology

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APA (6th Edition):

Liu, M. (2012). RNA oxidative damage and ribosomal RNA surveillance under oxidative stress. (Doctoral Dissertation). Florida Atlantic University. Retrieved from http://purl.flvc.org/FAU/3355620

Chicago Manual of Style (16th Edition):

Liu, Min. “RNA oxidative damage and ribosomal RNA surveillance under oxidative stress.” 2012. Doctoral Dissertation, Florida Atlantic University. Accessed September 22, 2020. http://purl.flvc.org/FAU/3355620.

MLA Handbook (7th Edition):

Liu, Min. “RNA oxidative damage and ribosomal RNA surveillance under oxidative stress.” 2012. Web. 22 Sep 2020.

Vancouver:

Liu M. RNA oxidative damage and ribosomal RNA surveillance under oxidative stress. [Internet] [Doctoral dissertation]. Florida Atlantic University; 2012. [cited 2020 Sep 22]. Available from: http://purl.flvc.org/FAU/3355620.

Council of Science Editors:

Liu M. RNA oxidative damage and ribosomal RNA surveillance under oxidative stress. [Doctoral Dissertation]. Florida Atlantic University; 2012. Available from: http://purl.flvc.org/FAU/3355620


Florida Atlantic University

24. Kumari, Neeta. GAD 65 and its role in pancreatic tissue survival.

Degree: MS, 2012, Florida Atlantic University

Summary: We employed three genotypes of GAD 65, wildtype (GAD 65 +/+), heterozygous (GAD 65 +/-) and knockout (GAD 65 -/-) to investigate the role… (more)

Subjects/Keywords: Glutamic acids – Antagonists; Cellular signal transduction; Glutamic acid – Metabolism

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APA (6th Edition):

Kumari, N. (2012). GAD 65 and its role in pancreatic tissue survival. (Masters Thesis). Florida Atlantic University. Retrieved from http://purl.flvc.org/FAU/3342206

Chicago Manual of Style (16th Edition):

Kumari, Neeta. “GAD 65 and its role in pancreatic tissue survival.” 2012. Masters Thesis, Florida Atlantic University. Accessed September 22, 2020. http://purl.flvc.org/FAU/3342206.

MLA Handbook (7th Edition):

Kumari, Neeta. “GAD 65 and its role in pancreatic tissue survival.” 2012. Web. 22 Sep 2020.

Vancouver:

Kumari N. GAD 65 and its role in pancreatic tissue survival. [Internet] [Masters thesis]. Florida Atlantic University; 2012. [cited 2020 Sep 22]. Available from: http://purl.flvc.org/FAU/3342206.

Council of Science Editors:

Kumari N. GAD 65 and its role in pancreatic tissue survival. [Masters Thesis]. Florida Atlantic University; 2012. Available from: http://purl.flvc.org/FAU/3342206


Florida Atlantic University

25. John, Ciny. Determining the subcellular localization of a group II p21-activated kinase - PAK6.

Degree: MS, 2012, Florida Atlantic University

Summary: p-21-activated kinase 6 (PAK6) is a serine-threonine protein kinase originally identified as an Androgen Receptor (AR) interacting protein. In current study, we determined the… (more)

Subjects/Keywords: Cellular signal transduction; Serine proteinases; Phosphorylation; Protein kinases – Pathophysiology; Phosphoroproteins – Metabolism

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APA (6th Edition):

John, C. (2012). Determining the subcellular localization of a group II p21-activated kinase - PAK6. (Masters Thesis). Florida Atlantic University. Retrieved from http://purl.flvc.org/FAU/3355569

Chicago Manual of Style (16th Edition):

John, Ciny. “Determining the subcellular localization of a group II p21-activated kinase - PAK6.” 2012. Masters Thesis, Florida Atlantic University. Accessed September 22, 2020. http://purl.flvc.org/FAU/3355569.

MLA Handbook (7th Edition):

John, Ciny. “Determining the subcellular localization of a group II p21-activated kinase - PAK6.” 2012. Web. 22 Sep 2020.

Vancouver:

John C. Determining the subcellular localization of a group II p21-activated kinase - PAK6. [Internet] [Masters thesis]. Florida Atlantic University; 2012. [cited 2020 Sep 22]. Available from: http://purl.flvc.org/FAU/3355569.

Council of Science Editors:

John C. Determining the subcellular localization of a group II p21-activated kinase - PAK6. [Masters Thesis]. Florida Atlantic University; 2012. Available from: http://purl.flvc.org/FAU/3355569


Washington University in St. Louis

26. Roh, Hyun Cheol. Analysis of Zinc Transporters in C. elegans.

Degree: PhD, Biology and Biomedical Sciences: Molecular Cell Biology, 2011, Washington University in St. Louis

 Zinc is a trace element essential for organisms, and organisms have homeostatic mechanisms to control zinc metabolism. Zinc metabolism is mediated by numerous proteins including… (more)

Subjects/Keywords: Genetics; Cellular Biology; Molecular Biology; C. elegans; Zinc Metabolism; Zinc Transporters

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APA (6th Edition):

Roh, H. C. (2011). Analysis of Zinc Transporters in C. elegans. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/875

Chicago Manual of Style (16th Edition):

Roh, Hyun Cheol. “Analysis of Zinc Transporters in C. elegans.” 2011. Doctoral Dissertation, Washington University in St. Louis. Accessed September 22, 2020. https://openscholarship.wustl.edu/etd/875.

MLA Handbook (7th Edition):

Roh, Hyun Cheol. “Analysis of Zinc Transporters in C. elegans.” 2011. Web. 22 Sep 2020.

Vancouver:

Roh HC. Analysis of Zinc Transporters in C. elegans. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2011. [cited 2020 Sep 22]. Available from: https://openscholarship.wustl.edu/etd/875.

Council of Science Editors:

Roh HC. Analysis of Zinc Transporters in C. elegans. [Doctoral Dissertation]. Washington University in St. Louis; 2011. Available from: https://openscholarship.wustl.edu/etd/875


University of South Florida

27. Marking, Devon Nicole. Exploring the Role of Intracellular Aminopeptidases in Staphylococcus aureus Pathogenesis.

Degree: 2015, University of South Florida

 Staphylococcus aureus is a remarkably pathogenic bacterium that is widely prevalent among the human population. It is the leading agent of skin and soft tissue… (more)

Subjects/Keywords: Protease; Cellular Nutrition; Metabolism; Mass Spectrometry; N-Terminomics; Microbiology; Molecular Biology

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APA (6th Edition):

Marking, D. N. (2015). Exploring the Role of Intracellular Aminopeptidases in Staphylococcus aureus Pathogenesis. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5852

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):

Marking, Devon Nicole. “Exploring the Role of Intracellular Aminopeptidases in Staphylococcus aureus Pathogenesis.” 2015. Thesis, University of South Florida. Accessed September 22, 2020. https://scholarcommons.usf.edu/etd/5852.

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

MLA Handbook (7th Edition):

Marking, Devon Nicole. “Exploring the Role of Intracellular Aminopeptidases in Staphylococcus aureus Pathogenesis.” 2015. Web. 22 Sep 2020.

Vancouver:

Marking DN. Exploring the Role of Intracellular Aminopeptidases in Staphylococcus aureus Pathogenesis. [Internet] [Thesis]. University of South Florida; 2015. [cited 2020 Sep 22]. Available from: https://scholarcommons.usf.edu/etd/5852.

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

Council of Science Editors:

Marking DN. Exploring the Role of Intracellular Aminopeptidases in Staphylococcus aureus Pathogenesis. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5852

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


Universidad de Extremadura

28. Martín Hidalgo, David. Fisiología celular y calidad seminal durante la conservación del semen porcino refrigerado .

Degree: 2013, Universidad de Extremadura

 La Inseminación Artificial con semen diluido refrigerado es una de las tecnologías de la reproducción más utilizadas en el ganado porcino. Para un máximo aprovechamiento… (more)

Subjects/Keywords: Reproducción; Antioxidantes; Metabolismo celular; Reproduction; Antioxidants; Cellular metabolism; Semen; Sperm

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APA (6th Edition):

Martín Hidalgo, D. (2013). Fisiología celular y calidad seminal durante la conservación del semen porcino refrigerado . (Thesis). Universidad de Extremadura. Retrieved from http://hdl.handle.net/10662/799

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):

Martín Hidalgo, David. “Fisiología celular y calidad seminal durante la conservación del semen porcino refrigerado .” 2013. Thesis, Universidad de Extremadura. Accessed September 22, 2020. http://hdl.handle.net/10662/799.

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

MLA Handbook (7th Edition):

Martín Hidalgo, David. “Fisiología celular y calidad seminal durante la conservación del semen porcino refrigerado .” 2013. Web. 22 Sep 2020.

Vancouver:

Martín Hidalgo D. Fisiología celular y calidad seminal durante la conservación del semen porcino refrigerado . [Internet] [Thesis]. Universidad de Extremadura; 2013. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/10662/799.

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

Council of Science Editors:

Martín Hidalgo D. Fisiología celular y calidad seminal durante la conservación del semen porcino refrigerado . [Thesis]. Universidad de Extremadura; 2013. Available from: http://hdl.handle.net/10662/799

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


Duke University

29. McDonnell, Eoin. The Role of Acetylation in the Metabolic Reprogramming of Cancer Cells .

Degree: 2016, Duke University

  Identifying metabolic vulnerabilities of cancer cells remains a subject of investigation for the identification of potential metabolically based therapies for cancer. It is well… (more)

Subjects/Keywords: Molecular biology; Pharmacology; Cellular biology; Acetylation; Cancer; Epigenetics; Histone; Metabolism

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

APA (6th Edition):

McDonnell, E. (2016). The Role of Acetylation in the Metabolic Reprogramming of Cancer Cells . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/13387

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):

McDonnell, Eoin. “The Role of Acetylation in the Metabolic Reprogramming of Cancer Cells .” 2016. Thesis, Duke University. Accessed September 22, 2020. http://hdl.handle.net/10161/13387.

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

MLA Handbook (7th Edition):

McDonnell, Eoin. “The Role of Acetylation in the Metabolic Reprogramming of Cancer Cells .” 2016. Web. 22 Sep 2020.

Vancouver:

McDonnell E. The Role of Acetylation in the Metabolic Reprogramming of Cancer Cells . [Internet] [Thesis]. Duke University; 2016. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/10161/13387.

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

Council of Science Editors:

McDonnell E. The Role of Acetylation in the Metabolic Reprogramming of Cancer Cells . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/13387

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

30. Budzowska, Magdalena. Cellular Responses to Replication Problems.

Degree: Department of Molecular Genetics, 2008, Erasmus University Medical Center

 textabstractDuring every S-phase cells need to duplicate their genomes so that both daughter cells inherit complete copies of genetic information. It is a tremendous task,… (more)

Subjects/Keywords: DNA; cellular metabolism; genomes

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

APA (6th Edition):

Budzowska, M. (2008). Cellular Responses to Replication Problems. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/20412

Chicago Manual of Style (16th Edition):

Budzowska, Magdalena. “Cellular Responses to Replication Problems.” 2008. Doctoral Dissertation, Erasmus University Medical Center. Accessed September 22, 2020. http://hdl.handle.net/1765/20412.

MLA Handbook (7th Edition):

Budzowska, Magdalena. “Cellular Responses to Replication Problems.” 2008. Web. 22 Sep 2020.

Vancouver:

Budzowska M. Cellular Responses to Replication Problems. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 2008. [cited 2020 Sep 22]. Available from: http://hdl.handle.net/1765/20412.

Council of Science Editors:

Budzowska M. Cellular Responses to Replication Problems. [Doctoral Dissertation]. Erasmus University Medical Center; 2008. Available from: http://hdl.handle.net/1765/20412

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