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You searched for +publisher:"Duke University" +contributor:("Chi, Jen-Tsan A"). Showing records 1 – 5 of 5 total matches.

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Duke University

1. Doss, Jennifer. The Erythrocyte Transcriptome: Global Characterization and Therapeutic Implication .

Degree: 2015, Duke University

  A blood draw is one of the most readily accessible, commonly practiced medical procedures with biomarker utility. In particular, transcriptome signatures of blood cells… (more)

Subjects/Keywords: Genetics

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

APA (6th Edition):

Doss, J. (2015). The Erythrocyte Transcriptome: Global Characterization and Therapeutic Implication . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9812

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):

Doss, Jennifer. “The Erythrocyte Transcriptome: Global Characterization and Therapeutic Implication .” 2015. Thesis, Duke University. Accessed February 27, 2020. http://hdl.handle.net/10161/9812.

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

MLA Handbook (7th Edition):

Doss, Jennifer. “The Erythrocyte Transcriptome: Global Characterization and Therapeutic Implication .” 2015. Web. 27 Feb 2020.

Vancouver:

Doss J. The Erythrocyte Transcriptome: Global Characterization and Therapeutic Implication . [Internet] [Thesis]. Duke University; 2015. [cited 2020 Feb 27]. Available from: http://hdl.handle.net/10161/9812.

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

Council of Science Editors:

Doss J. The Erythrocyte Transcriptome: Global Characterization and Therapeutic Implication . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/9812

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


Duke University

2. Jiang, Xiaolei. Genomic Analysis of Cancer Heterogeneity and Oncogenic Mechanisms .

Degree: 2014, Duke University

  The development of cancer is a process by which an accumulation of genetic changes leads to uncontrolled replication of cells. Since the process of… (more)

Subjects/Keywords: Genetics; Molecular biology; Cancer; Mechanism; Oncogene; Therapeutics

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

APA (6th Edition):

Jiang, X. (2014). Genomic Analysis of Cancer Heterogeneity and Oncogenic Mechanisms . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9421

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):

Jiang, Xiaolei. “Genomic Analysis of Cancer Heterogeneity and Oncogenic Mechanisms .” 2014. Thesis, Duke University. Accessed February 27, 2020. http://hdl.handle.net/10161/9421.

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

MLA Handbook (7th Edition):

Jiang, Xiaolei. “Genomic Analysis of Cancer Heterogeneity and Oncogenic Mechanisms .” 2014. Web. 27 Feb 2020.

Vancouver:

Jiang X. Genomic Analysis of Cancer Heterogeneity and Oncogenic Mechanisms . [Internet] [Thesis]. Duke University; 2014. [cited 2020 Feb 27]. Available from: http://hdl.handle.net/10161/9421.

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

Council of Science Editors:

Jiang X. Genomic Analysis of Cancer Heterogeneity and Oncogenic Mechanisms . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/9421

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


Duke University

3. LaMonte, Greg. The Role of Erythrocytic miRNA in the lifecycle of Plasmodium falciparum .

Degree: 2012, Duke University

  Malaria, caused by the apicomplexan parasite Plasmodium, is a disease which affects up to 500 million people each year. Historically, malaria infection has been… (more)

Subjects/Keywords: Parasitology; Genetics; Host-Pathogen Interactions; Malaria; miRNA; Sickle Cell Disease

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

APA (6th Edition):

LaMonte, G. (2012). The Role of Erythrocytic miRNA in the lifecycle of Plasmodium falciparum . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5783

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):

LaMonte, Greg. “The Role of Erythrocytic miRNA in the lifecycle of Plasmodium falciparum .” 2012. Thesis, Duke University. Accessed February 27, 2020. http://hdl.handle.net/10161/5783.

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

MLA Handbook (7th Edition):

LaMonte, Greg. “The Role of Erythrocytic miRNA in the lifecycle of Plasmodium falciparum .” 2012. Web. 27 Feb 2020.

Vancouver:

LaMonte G. The Role of Erythrocytic miRNA in the lifecycle of Plasmodium falciparum . [Internet] [Thesis]. Duke University; 2012. [cited 2020 Feb 27]. Available from: http://hdl.handle.net/10161/5783.

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

Council of Science Editors:

LaMonte G. The Role of Erythrocytic miRNA in the lifecycle of Plasmodium falciparum . [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/5783

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


Duke University

4. Ding, Chien-Kuang Cornelia. Regulation of Ferroptosis by a novel NADPH phosphatase MESH1 .

Degree: 2019, Duke University

  Ferroptosis is a form of regulated cell death featured by lipid peroxidation and breakage of cell membrane. However, the molecular mediators and regulators are… (more)

Subjects/Keywords: Biochemistry; Molecular biology; Ferroptosis; HDDC3; MESH1; NADPH

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

APA (6th Edition):

Ding, C. C. (2019). Regulation of Ferroptosis by a novel NADPH phosphatase MESH1 . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/18658

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):

Ding, Chien-Kuang Cornelia. “Regulation of Ferroptosis by a novel NADPH phosphatase MESH1 .” 2019. Thesis, Duke University. Accessed February 27, 2020. http://hdl.handle.net/10161/18658.

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

MLA Handbook (7th Edition):

Ding, Chien-Kuang Cornelia. “Regulation of Ferroptosis by a novel NADPH phosphatase MESH1 .” 2019. Web. 27 Feb 2020.

Vancouver:

Ding CC. Regulation of Ferroptosis by a novel NADPH phosphatase MESH1 . [Internet] [Thesis]. Duke University; 2019. [cited 2020 Feb 27]. Available from: http://hdl.handle.net/10161/18658.

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

Council of Science Editors:

Ding CC. Regulation of Ferroptosis by a novel NADPH phosphatase MESH1 . [Thesis]. Duke University; 2019. Available from: http://hdl.handle.net/10161/18658

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


Duke University

5. Levitt, Brandt E. Drug Development in Dengue Virus and Molecular Epidemiology of Malaria in Western Kenya .

Degree: 2017, Duke University

  Dengue viruses (DENV) and other mosquito-borne flaviviruses are rapidly emerging human pathogens that threaten nearly half of the world’s population. There is currently no… (more)

Subjects/Keywords: Microbiology; Molecular biology; Epidemiology; Dengue; Drug; Gene; Malaria; Surveillance

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

APA (6th Edition):

Levitt, B. E. (2017). Drug Development in Dengue Virus and Molecular Epidemiology of Malaria in Western Kenya . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/14446

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):

Levitt, Brandt E. “Drug Development in Dengue Virus and Molecular Epidemiology of Malaria in Western Kenya .” 2017. Thesis, Duke University. Accessed February 27, 2020. http://hdl.handle.net/10161/14446.

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

MLA Handbook (7th Edition):

Levitt, Brandt E. “Drug Development in Dengue Virus and Molecular Epidemiology of Malaria in Western Kenya .” 2017. Web. 27 Feb 2020.

Vancouver:

Levitt BE. Drug Development in Dengue Virus and Molecular Epidemiology of Malaria in Western Kenya . [Internet] [Thesis]. Duke University; 2017. [cited 2020 Feb 27]. Available from: http://hdl.handle.net/10161/14446.

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

Council of Science Editors:

Levitt BE. Drug Development in Dengue Virus and Molecular Epidemiology of Malaria in Western Kenya . [Thesis]. Duke University; 2017. Available from: http://hdl.handle.net/10161/14446

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

.