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You searched for +publisher:"Clemson University" +contributor:("Dr. Yanzhang Wei"). Showing records 1 – 6 of 6 total matches.

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1. Pennington-Krygier, Chelsea Anne. Interleukin-12/HFasTI: A Humanized Bifunctional Fusion Protein For Cancer Immunotherapy.

Degree: MS, Biological Sciences, 2017, Clemson University

 Cancer remains a major health issue worldwide, and the leading cause of death in nearly half the states in America. As our understanding of the… (more)

Subjects/Keywords: apoptosis; cancer; Fas; immunotherapy; Interleukin 12; natural killer cells

Clemson University Genomics Institute. Cells Human embryonic kidney cells HEK293 (ATCC No… …by double restriction enzyme digest and DNA sequencing at Clemson University Genomics… …confirmed by double restriction enzyme digest and DNA sequencing at Clemson University Genomics… 

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APA (6th Edition):

Pennington-Krygier, C. A. (2017). Interleukin-12/HFasTI: A Humanized Bifunctional Fusion Protein For Cancer Immunotherapy. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/2777

Chicago Manual of Style (16th Edition):

Pennington-Krygier, Chelsea Anne. “Interleukin-12/HFasTI: A Humanized Bifunctional Fusion Protein For Cancer Immunotherapy.” 2017. Masters Thesis, Clemson University. Accessed October 28, 2020. https://tigerprints.clemson.edu/all_theses/2777.

MLA Handbook (7th Edition):

Pennington-Krygier, Chelsea Anne. “Interleukin-12/HFasTI: A Humanized Bifunctional Fusion Protein For Cancer Immunotherapy.” 2017. Web. 28 Oct 2020.

Vancouver:

Pennington-Krygier CA. Interleukin-12/HFasTI: A Humanized Bifunctional Fusion Protein For Cancer Immunotherapy. [Internet] [Masters thesis]. Clemson University; 2017. [cited 2020 Oct 28]. Available from: https://tigerprints.clemson.edu/all_theses/2777.

Council of Science Editors:

Pennington-Krygier CA. Interleukin-12/HFasTI: A Humanized Bifunctional Fusion Protein For Cancer Immunotherapy. [Masters Thesis]. Clemson University; 2017. Available from: https://tigerprints.clemson.edu/all_theses/2777

2. Anderson, Amy Lauren. The Effects of Indirubin-3’-(2,3 dihydroxypropyl)-oximether (E804) on Inflammation Profile in Macrophages.

Degree: PhD, Environmental Toxicology, 2014, Clemson University

  Indirubin is a deep-red bis-indole isomer of indigo blue, both of which are biologically active ingredients in Danggui Longhui Wan, an ancient Chinese herbal… (more)

Subjects/Keywords: Toxicology

…Program in Environmental Toxicology Clemson University, Clemson SC USA 29634 16 Pages 19… 

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APA (6th Edition):

Anderson, A. L. (2014). The Effects of Indirubin-3’-(2,3 dihydroxypropyl)-oximether (E804) on Inflammation Profile in Macrophages. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1407

Chicago Manual of Style (16th Edition):

Anderson, Amy Lauren. “The Effects of Indirubin-3’-(2,3 dihydroxypropyl)-oximether (E804) on Inflammation Profile in Macrophages.” 2014. Doctoral Dissertation, Clemson University. Accessed October 28, 2020. https://tigerprints.clemson.edu/all_dissertations/1407.

MLA Handbook (7th Edition):

Anderson, Amy Lauren. “The Effects of Indirubin-3’-(2,3 dihydroxypropyl)-oximether (E804) on Inflammation Profile in Macrophages.” 2014. Web. 28 Oct 2020.

Vancouver:

Anderson AL. The Effects of Indirubin-3’-(2,3 dihydroxypropyl)-oximether (E804) on Inflammation Profile in Macrophages. [Internet] [Doctoral dissertation]. Clemson University; 2014. [cited 2020 Oct 28]. Available from: https://tigerprints.clemson.edu/all_dissertations/1407.

Council of Science Editors:

Anderson AL. The Effects of Indirubin-3’-(2,3 dihydroxypropyl)-oximether (E804) on Inflammation Profile in Macrophages. [Doctoral Dissertation]. Clemson University; 2014. Available from: https://tigerprints.clemson.edu/all_dissertations/1407

3. Guha, Sujay. Studies of Molecular Mechanisms of Cranberry Mediated Healthspan Promotion in Caenorhabditis Elegans.

Degree: PhD, Microbiology, 2013, Clemson University

  Extensive studies have demonstrated the potent ability of many nutraceuticals to alleviate the symptoms of aging and stress. We found that cranberry extract (CBE)… (more)

Subjects/Keywords: Microbiology

…Department of Biological Sciences, Clemson University, Clemson, SC 29634, USA 2 Institute 3 for… …Engaged Aging, Clemson University, Clemson, SC 29634, USA Laboratory of Experimental… 

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APA (6th Edition):

Guha, S. (2013). Studies of Molecular Mechanisms of Cranberry Mediated Healthspan Promotion in Caenorhabditis Elegans. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1408

Chicago Manual of Style (16th Edition):

Guha, Sujay. “Studies of Molecular Mechanisms of Cranberry Mediated Healthspan Promotion in Caenorhabditis Elegans.” 2013. Doctoral Dissertation, Clemson University. Accessed October 28, 2020. https://tigerprints.clemson.edu/all_dissertations/1408.

MLA Handbook (7th Edition):

Guha, Sujay. “Studies of Molecular Mechanisms of Cranberry Mediated Healthspan Promotion in Caenorhabditis Elegans.” 2013. Web. 28 Oct 2020.

Vancouver:

Guha S. Studies of Molecular Mechanisms of Cranberry Mediated Healthspan Promotion in Caenorhabditis Elegans. [Internet] [Doctoral dissertation]. Clemson University; 2013. [cited 2020 Oct 28]. Available from: https://tigerprints.clemson.edu/all_dissertations/1408.

Council of Science Editors:

Guha S. Studies of Molecular Mechanisms of Cranberry Mediated Healthspan Promotion in Caenorhabditis Elegans. [Doctoral Dissertation]. Clemson University; 2013. Available from: https://tigerprints.clemson.edu/all_dissertations/1408

4. Yang, Xi. Novel Fusion Protein IL-12/FasTI for Cancer Immunogene Therapy.

Degree: PhD, Biological Sciences, 2018, Clemson University

 Cancer immunotherapies using cytokines demonstrated effective in previous studies, whereas one major obstacle with the strategy is the severe side effects when administrated systemically at… (more)

Subjects/Keywords: Apoptosis; cancer immunotherapy; Fas; IL-12; Lentivirus; NK cell

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APA (6th Edition):

Yang, X. (2018). Novel Fusion Protein IL-12/FasTI for Cancer Immunogene Therapy. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/2092

Chicago Manual of Style (16th Edition):

Yang, Xi. “Novel Fusion Protein IL-12/FasTI for Cancer Immunogene Therapy.” 2018. Doctoral Dissertation, Clemson University. Accessed October 28, 2020. https://tigerprints.clemson.edu/all_dissertations/2092.

MLA Handbook (7th Edition):

Yang, Xi. “Novel Fusion Protein IL-12/FasTI for Cancer Immunogene Therapy.” 2018. Web. 28 Oct 2020.

Vancouver:

Yang X. Novel Fusion Protein IL-12/FasTI for Cancer Immunogene Therapy. [Internet] [Doctoral dissertation]. Clemson University; 2018. [cited 2020 Oct 28]. Available from: https://tigerprints.clemson.edu/all_dissertations/2092.

Council of Science Editors:

Yang X. Novel Fusion Protein IL-12/FasTI for Cancer Immunogene Therapy. [Doctoral Dissertation]. Clemson University; 2018. Available from: https://tigerprints.clemson.edu/all_dissertations/2092

5. Yang, Xi. INTERLEUKIN12/FASTI: A Novel Bi-Functional Fusion Protein for Cancer Immunogene Therapy.

Degree: MS, Biological Sciences, 2016, Clemson University

 Cancer is the second leading cause of disease death worldwide. Whereas cancer immunotherapy with cytokines in previous researches demonstrated effective in activating immune response against… (more)

Subjects/Keywords: apoptosis; cancer immunity; Fas; gene therapy; Interleukin-12; Natural killer cells

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

APA (6th Edition):

Yang, X. (2016). INTERLEUKIN12/FASTI: A Novel Bi-Functional Fusion Protein for Cancer Immunogene Therapy. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/2407

Chicago Manual of Style (16th Edition):

Yang, Xi. “INTERLEUKIN12/FASTI: A Novel Bi-Functional Fusion Protein for Cancer Immunogene Therapy.” 2016. Masters Thesis, Clemson University. Accessed October 28, 2020. https://tigerprints.clemson.edu/all_theses/2407.

MLA Handbook (7th Edition):

Yang, Xi. “INTERLEUKIN12/FASTI: A Novel Bi-Functional Fusion Protein for Cancer Immunogene Therapy.” 2016. Web. 28 Oct 2020.

Vancouver:

Yang X. INTERLEUKIN12/FASTI: A Novel Bi-Functional Fusion Protein for Cancer Immunogene Therapy. [Internet] [Masters thesis]. Clemson University; 2016. [cited 2020 Oct 28]. Available from: https://tigerprints.clemson.edu/all_theses/2407.

Council of Science Editors:

Yang X. INTERLEUKIN12/FASTI: A Novel Bi-Functional Fusion Protein for Cancer Immunogene Therapy. [Masters Thesis]. Clemson University; 2016. Available from: https://tigerprints.clemson.edu/all_theses/2407

6. Raval, Yash S. Application of Glycoconjugate-Functionalized Magnetic Nanoparticles as Potent Anti-Adhesion and Anti-Bacterial Agents.

Degree: PhD, Biological Sciences, 2017, Clemson University

 Magnetic nanoparticles (MNPs) are currently being extensively in multitude of biomedical applications on account of their exceptional biocompatibility. By attaching different targeting ligands/molecules, MNPs have… (more)

…O. Thompson Mefford, Clemson University) coined the term ‘magnetically mediated… 

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APA (6th Edition):

Raval, Y. S. (2017). Application of Glycoconjugate-Functionalized Magnetic Nanoparticles as Potent Anti-Adhesion and Anti-Bacterial Agents. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1964

Chicago Manual of Style (16th Edition):

Raval, Yash S. “Application of Glycoconjugate-Functionalized Magnetic Nanoparticles as Potent Anti-Adhesion and Anti-Bacterial Agents.” 2017. Doctoral Dissertation, Clemson University. Accessed October 28, 2020. https://tigerprints.clemson.edu/all_dissertations/1964.

MLA Handbook (7th Edition):

Raval, Yash S. “Application of Glycoconjugate-Functionalized Magnetic Nanoparticles as Potent Anti-Adhesion and Anti-Bacterial Agents.” 2017. Web. 28 Oct 2020.

Vancouver:

Raval YS. Application of Glycoconjugate-Functionalized Magnetic Nanoparticles as Potent Anti-Adhesion and Anti-Bacterial Agents. [Internet] [Doctoral dissertation]. Clemson University; 2017. [cited 2020 Oct 28]. Available from: https://tigerprints.clemson.edu/all_dissertations/1964.

Council of Science Editors:

Raval YS. Application of Glycoconjugate-Functionalized Magnetic Nanoparticles as Potent Anti-Adhesion and Anti-Bacterial Agents. [Doctoral Dissertation]. Clemson University; 2017. Available from: https://tigerprints.clemson.edu/all_dissertations/1964

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