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You searched for +publisher:"University of Southern California" +contributor:("Laird-Offringa, Ite A."). Showing records 1 – 23 of 23 total matches.

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University of Southern California

1. Alef-Omidy, Honey. DNA methylation markers for blood-based detection of small cell lung cancer in mouse models.

Degree: MS, Biochemistry and Molecular Biology, 2014, University of Southern California

 Lung cancer is the top cancer killer in the United States. This cancer starts in the cells lining the bronchi or other parts of the… (more)

Subjects/Keywords: small cell lung cancer; DNA methylation; biomarkers; mouse models; MethyLight; sodium bisulfite

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APA (6th Edition):

Alef-Omidy, H. (2014). DNA methylation markers for blood-based detection of small cell lung cancer in mouse models. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514619/rec/2068

Chicago Manual of Style (16th Edition):

Alef-Omidy, Honey. “DNA methylation markers for blood-based detection of small cell lung cancer in mouse models.” 2014. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514619/rec/2068.

MLA Handbook (7th Edition):

Alef-Omidy, Honey. “DNA methylation markers for blood-based detection of small cell lung cancer in mouse models.” 2014. Web. 21 Oct 2018.

Vancouver:

Alef-Omidy H. DNA methylation markers for blood-based detection of small cell lung cancer in mouse models. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514619/rec/2068.

Council of Science Editors:

Alef-Omidy H. DNA methylation markers for blood-based detection of small cell lung cancer in mouse models. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514619/rec/2068


University of Southern California

2. Chan, Nymph. Regulation of angiogenesis in choroidal neovascularization and proliferative vitreoretinopathy by histone acetylation.

Degree: PhD, Pathobiology, 2015, University of Southern California

 In Dr. Hinton’s laboratory, the main focuses of research are the leading blinding retinal diseases, including age-related macular degeneration (AMD) and proliferative vitreoretinopathy (PVR). These… (more)

Subjects/Keywords: age-related macular degeneration; choroidal neovascularization; proliferative vitreoretinopathy; retinal pigment epithelium; histone acetylation; trichostatin A

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APA (6th Edition):

Chan, N. (2015). Regulation of angiogenesis in choroidal neovascularization and proliferative vitreoretinopathy by histone acetylation. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/336799/rec/5482

Chicago Manual of Style (16th Edition):

Chan, Nymph. “Regulation of angiogenesis in choroidal neovascularization and proliferative vitreoretinopathy by histone acetylation.” 2015. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/336799/rec/5482.

MLA Handbook (7th Edition):

Chan, Nymph. “Regulation of angiogenesis in choroidal neovascularization and proliferative vitreoretinopathy by histone acetylation.” 2015. Web. 21 Oct 2018.

Vancouver:

Chan N. Regulation of angiogenesis in choroidal neovascularization and proliferative vitreoretinopathy by histone acetylation. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/336799/rec/5482.

Council of Science Editors:

Chan N. Regulation of angiogenesis in choroidal neovascularization and proliferative vitreoretinopathy by histone acetylation. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/336799/rec/5482


University of Southern California

3. Subramanian, Smita. Investigating the role of SASH1 gene located on chromosome 6 in ovarian cancer.

Degree: MS, Biochemistry & Molecular Biology, 2010, University of Southern California

 It is known that there is a strong interplay of various oncogenes and tumor suppressor genes underlying the mechanism of cancer formation and identifying these… (more)

Subjects/Keywords: ovarian cancer genetics; tumor suppressor genes

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APA (6th Edition):

Subramanian, S. (2010). Investigating the role of SASH1 gene located on chromosome 6 in ovarian cancer. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193090/rec/3631

Chicago Manual of Style (16th Edition):

Subramanian, Smita. “Investigating the role of SASH1 gene located on chromosome 6 in ovarian cancer.” 2010. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193090/rec/3631.

MLA Handbook (7th Edition):

Subramanian, Smita. “Investigating the role of SASH1 gene located on chromosome 6 in ovarian cancer.” 2010. Web. 21 Oct 2018.

Vancouver:

Subramanian S. Investigating the role of SASH1 gene located on chromosome 6 in ovarian cancer. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193090/rec/3631.

Council of Science Editors:

Subramanian S. Investigating the role of SASH1 gene located on chromosome 6 in ovarian cancer. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193090/rec/3631


University of Southern California

4. Selamat, Suhaida Adura. DNA methylation changes in the development of lung adenocarcinoma.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2012, University of Southern California

 Lung cancer accounted for 13% of total cancer cases and 18% of cancer deaths globally in 2008. The combination of increasing smoking prevalence in many… (more)

Subjects/Keywords: DNA methylation; lung adenocarcinoma; lung cancer; epigenetics

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APA (6th Edition):

Selamat, S. A. (2012). DNA methylation changes in the development of lung adenocarcinoma. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/2645/rec/2065

Chicago Manual of Style (16th Edition):

Selamat, Suhaida Adura. “DNA methylation changes in the development of lung adenocarcinoma.” 2012. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/2645/rec/2065.

MLA Handbook (7th Edition):

Selamat, Suhaida Adura. “DNA methylation changes in the development of lung adenocarcinoma.” 2012. Web. 21 Oct 2018.

Vancouver:

Selamat SA. DNA methylation changes in the development of lung adenocarcinoma. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/2645/rec/2065.

Council of Science Editors:

Selamat SA. DNA methylation changes in the development of lung adenocarcinoma. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/2645/rec/2065


University of Southern California

5. Si, Yuchen. Determinination of the causal potential of histone modifications on transcription and chromatin structure.

Degree: MS, Biochemistry and Molecular Biology, 2012, University of Southern California

 Histone modification is a major epigenetic regulatory mechanism that controls chromatin structure and gene expression potential. However, the causal potential of individual histone modifications remains… (more)

Subjects/Keywords: histone modification; G9a; Suv39h1; Suv39h2; Pr-set7; transcription; chromatin structure

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APA (6th Edition):

Si, Y. (2012). Determinination of the causal potential of histone modifications on transcription and chromatin structure. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/62768/rec/1890

Chicago Manual of Style (16th Edition):

Si, Yuchen. “Determinination of the causal potential of histone modifications on transcription and chromatin structure.” 2012. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/62768/rec/1890.

MLA Handbook (7th Edition):

Si, Yuchen. “Determinination of the causal potential of histone modifications on transcription and chromatin structure.” 2012. Web. 21 Oct 2018.

Vancouver:

Si Y. Determinination of the causal potential of histone modifications on transcription and chromatin structure. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/62768/rec/1890.

Council of Science Editors:

Si Y. Determinination of the causal potential of histone modifications on transcription and chromatin structure. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/62768/rec/1890


University of Southern California

6. Houshdaran, Sahar. DNA methylation as a biomarker in human reproductive health and disease.

Degree: PhD, Biochemistry & Molecular Biology, 2011, University of Southern California

 Epigenetics refers to the changes in gene expression that are not accounted for by the changes in DNA sequence. DNA methylation is one of the… (more)

Subjects/Keywords: DNA methylation; epigenetics; ovarian cancer; ovarian carcinoma; male infertility; sperm epigenetics

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APA (6th Edition):

Houshdaran, S. (2011). DNA methylation as a biomarker in human reproductive health and disease. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/254394/rec/2064

Chicago Manual of Style (16th Edition):

Houshdaran, Sahar. “DNA methylation as a biomarker in human reproductive health and disease.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/254394/rec/2064.

MLA Handbook (7th Edition):

Houshdaran, Sahar. “DNA methylation as a biomarker in human reproductive health and disease.” 2011. Web. 21 Oct 2018.

Vancouver:

Houshdaran S. DNA methylation as a biomarker in human reproductive health and disease. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/254394/rec/2064.

Council of Science Editors:

Houshdaran S. DNA methylation as a biomarker in human reproductive health and disease. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/254394/rec/2064


University of Southern California

7. Chen, Po-Han. The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b.

Degree: MS, Biochemistry & Molecular Biology, 2011, University of Southern California

 Mehtyl-CpG binding domain protein 2 and 3 (MBD2 and MBD3) contain methyl-CpG binding domains (MBD) and belong to a family of MBD proteins. Methyl-CpG binding… (more)

Subjects/Keywords: MBD protein; methyl-CpG

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APA (6th Edition):

Chen, P. (2011). The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6924

Chicago Manual of Style (16th Edition):

Chen, Po-Han. “The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b.” 2011. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6924.

MLA Handbook (7th Edition):

Chen, Po-Han. “The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b.” 2011. Web. 21 Oct 2018.

Vancouver:

Chen P. The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6924.

Council of Science Editors:

Chen P. The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6924


University of Southern California

8. Rhie, Suhn Kyong. Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2013, University of Southern California

 Breast Cancer (BCa) genome-wide association studies (GWAS) revealed allelic frequency differences between cases and controls at index single nucleotide polymorphisms (SNPs). To date 71 loci… (more)

Subjects/Keywords: breast cancer; GWAS; enhancer; single nucleotide polymorphism; epigenetics; predisposition

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APA (6th Edition):

Rhie, S. K. (2013). Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161

Chicago Manual of Style (16th Edition):

Rhie, Suhn Kyong. “Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161.

MLA Handbook (7th Edition):

Rhie, Suhn Kyong. “Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci.” 2013. Web. 21 Oct 2018.

Vancouver:

Rhie SK. Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161.

Council of Science Editors:

Rhie SK. Breast epithelial cell type specific enhancers and functional annotation of breast cancer risk loci. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/241673/rec/1161


University of Southern California

9. Kazarian, Meleeneh. Anti-Hu immuno-responsivenss in small-cell lung cancer.

Degree: PhD, Genetic, Molecular & Cellular Biology, 2010, University of Southern California

 Small-cell lung cancer (SCLC), which accounts for up to 15% of all lung cancers, is the most aggressive lung cancer subtype and lacks effective early… (more)

Subjects/Keywords: anti-Hu; autoantibody; autoantigen; small-cell lung cancer; isoaspartylation; mouse model

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APA (6th Edition):

Kazarian, M. (2010). Anti-Hu immuno-responsivenss in small-cell lung cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/411355/rec/840

Chicago Manual of Style (16th Edition):

Kazarian, Meleeneh. “Anti-Hu immuno-responsivenss in small-cell lung cancer.” 2010. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/411355/rec/840.

MLA Handbook (7th Edition):

Kazarian, Meleeneh. “Anti-Hu immuno-responsivenss in small-cell lung cancer.” 2010. Web. 21 Oct 2018.

Vancouver:

Kazarian M. Anti-Hu immuno-responsivenss in small-cell lung cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/411355/rec/840.

Council of Science Editors:

Kazarian M. Anti-Hu immuno-responsivenss in small-cell lung cancer. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/411355/rec/840


University of Southern California

10. Hung, Kuo-Chan. Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2014, University of Southern California

 mRNA display is an in vitro selection technique that can evolve novel ligands to modulating protein-protein interactions and regulate crucial biological functions. Previous efforts have… (more)

Subjects/Keywords: mRNA display; in vitro selection technique; G protein-coupled receptors; β 2AR; DC-SIGN; cancer vaccine; Dendritic cells; fibronectin scaffold

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APA (6th Edition):

Hung, K. (2014). Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1909

Chicago Manual of Style (16th Edition):

Hung, Kuo-Chan. “Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN.” 2014. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1909.

MLA Handbook (7th Edition):

Hung, Kuo-Chan. “Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN.” 2014. Web. 21 Oct 2018.

Vancouver:

Hung K. Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1909.

Council of Science Editors:

Hung K. Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1909


University of Southern California

11. Ankala, Ramya S. Investigating the function and epigenetic regulation of ABCA3, a novel LUAD tumor suppressor gene.

Degree: MS, Biochemistry and Molecular Biology, 2015, University of Southern California

 Lung cancer accounts for the majority of cancer deaths in the US and worldwide. Lung adenocarcinoma (LUAD) is the most common histological subtype of non-small… (more)

Subjects/Keywords: epigenetics; lung adenocarcinoma; ABCA3; ABCA17p; psuedogenes; epigenetic regulation

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APA (6th Edition):

Ankala, R. S. (2015). Investigating the function and epigenetic regulation of ABCA3, a novel LUAD tumor suppressor gene. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/614637/rec/3625

Chicago Manual of Style (16th Edition):

Ankala, Ramya S. “Investigating the function and epigenetic regulation of ABCA3, a novel LUAD tumor suppressor gene.” 2015. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/614637/rec/3625.

MLA Handbook (7th Edition):

Ankala, Ramya S. “Investigating the function and epigenetic regulation of ABCA3, a novel LUAD tumor suppressor gene.” 2015. Web. 21 Oct 2018.

Vancouver:

Ankala RS. Investigating the function and epigenetic regulation of ABCA3, a novel LUAD tumor suppressor gene. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/614637/rec/3625.

Council of Science Editors:

Ankala RS. Investigating the function and epigenetic regulation of ABCA3, a novel LUAD tumor suppressor gene. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/614637/rec/3625


University of Southern California

12. Johnson, Candace Jeanette-Sukey. CpG poor promoter SULT1C2 regulated by DNA methylation and is induced by cigarette smoke condensate in lung cell lines.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2017, University of Southern California

 We used the Illumina Infinium HumanMethylation27 BeadChip to investigate DNA methylation in lung cancer tissue and adjacent non tumor lung (AdjNTL) from sixty subjects with… (more)

Subjects/Keywords: SULT1C2; DNA methylation; non-CpG island promoter

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APA (6th Edition):

Johnson, C. J. (2017). CpG poor promoter SULT1C2 regulated by DNA methylation and is induced by cigarette smoke condensate in lung cell lines. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/604118/rec/1681

Chicago Manual of Style (16th Edition):

Johnson, Candace Jeanette-Sukey. “CpG poor promoter SULT1C2 regulated by DNA methylation and is induced by cigarette smoke condensate in lung cell lines.” 2017. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/604118/rec/1681.

MLA Handbook (7th Edition):

Johnson, Candace Jeanette-Sukey. “CpG poor promoter SULT1C2 regulated by DNA methylation and is induced by cigarette smoke condensate in lung cell lines.” 2017. Web. 21 Oct 2018.

Vancouver:

Johnson CJ. CpG poor promoter SULT1C2 regulated by DNA methylation and is induced by cigarette smoke condensate in lung cell lines. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/604118/rec/1681.

Council of Science Editors:

Johnson CJ. CpG poor promoter SULT1C2 regulated by DNA methylation and is induced by cigarette smoke condensate in lung cell lines. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/604118/rec/1681


University of Southern California

13. Oghamian, Shirley. The role of DNA methylation in early detection and progression of pancreatic cancer.

Degree: PhD, Biochemistry & Molecular Biology, 2011, University of Southern California

 Cancer is the second leading cause of death in the United States and each year nearly half a million Americans die of the disease. The… (more)

Subjects/Keywords: DNA methylation; pancreatic cancer; progression; early detection

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APA (6th Edition):

Oghamian, S. (2011). The role of DNA methylation in early detection and progression of pancreatic cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/242078/rec/7202

Chicago Manual of Style (16th Edition):

Oghamian, Shirley. “The role of DNA methylation in early detection and progression of pancreatic cancer.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/242078/rec/7202.

MLA Handbook (7th Edition):

Oghamian, Shirley. “The role of DNA methylation in early detection and progression of pancreatic cancer.” 2011. Web. 21 Oct 2018.

Vancouver:

Oghamian S. The role of DNA methylation in early detection and progression of pancreatic cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/242078/rec/7202.

Council of Science Editors:

Oghamian S. The role of DNA methylation in early detection and progression of pancreatic cancer. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/242078/rec/7202


University of Southern California

14. Khanna, Akshat. Characterizing the physiological roles and regulatory mechanisms of Maf1.

Degree: PhD, Molecular Biology, 2015, University of Southern California

 Obesity has become markedly more prevalent over the past two decades among developed countries however, the molecular events that connect obesity, lipid deregulation and human… (more)

Subjects/Keywords: obesity; RNA pol III; transcription

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APA (6th Edition):

Khanna, A. (2015). Characterizing the physiological roles and regulatory mechanisms of Maf1. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/563262/rec/1317

Chicago Manual of Style (16th Edition):

Khanna, Akshat. “Characterizing the physiological roles and regulatory mechanisms of Maf1.” 2015. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/563262/rec/1317.

MLA Handbook (7th Edition):

Khanna, Akshat. “Characterizing the physiological roles and regulatory mechanisms of Maf1.” 2015. Web. 21 Oct 2018.

Vancouver:

Khanna A. Characterizing the physiological roles and regulatory mechanisms of Maf1. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/563262/rec/1317.

Council of Science Editors:

Khanna A. Characterizing the physiological roles and regulatory mechanisms of Maf1. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/563262/rec/1317


University of Southern California

15. Wu, Shumin. Characterization and functional study of a novel human protein SFMBT, and PR-Set7 histone methyltransferase.

Degree: PhD, Biochemistry & Molecular Biology, 2010, University of Southern California

 Eukaryotic chromatin, a dynamic structure composed of DNA and chromatin-associated proteins, plays an essential role in key biological processes including gene transcription, cell cycle progression… (more)

Subjects/Keywords: PR-Set7; APC; Cdk1; Cdc14; cell cycle; chromatin

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APA (6th Edition):

Wu, S. (2010). Characterization and functional study of a novel human protein SFMBT, and PR-Set7 histone methyltransferase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/410757/rec/1292

Chicago Manual of Style (16th Edition):

Wu, Shumin. “Characterization and functional study of a novel human protein SFMBT, and PR-Set7 histone methyltransferase.” 2010. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/410757/rec/1292.

MLA Handbook (7th Edition):

Wu, Shumin. “Characterization and functional study of a novel human protein SFMBT, and PR-Set7 histone methyltransferase.” 2010. Web. 21 Oct 2018.

Vancouver:

Wu S. Characterization and functional study of a novel human protein SFMBT, and PR-Set7 histone methyltransferase. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/410757/rec/1292.

Council of Science Editors:

Wu S. Characterization and functional study of a novel human protein SFMBT, and PR-Set7 histone methyltransferase. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/410757/rec/1292


University of Southern California

16. Tomasian, Vanina. A new method to assess presence of SV40 in malignant mesothelioma.

Degree: MS, Biochemistry & Molecular Biology, 2006, University of Southern California

 Malignant mesothelioma, a tumor of the serosal lining of the pleura, pericardium and peritoneum, is a worldwide problem. Simian virus 40 (SV40) has been implicated… (more)

Subjects/Keywords: malignant mesothelioma

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APA (6th Edition):

Tomasian, V. (2006). A new method to assess presence of SV40 in malignant mesothelioma. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/26565/rec/275

Chicago Manual of Style (16th Edition):

Tomasian, Vanina. “A new method to assess presence of SV40 in malignant mesothelioma.” 2006. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/26565/rec/275.

MLA Handbook (7th Edition):

Tomasian, Vanina. “A new method to assess presence of SV40 in malignant mesothelioma.” 2006. Web. 21 Oct 2018.

Vancouver:

Tomasian V. A new method to assess presence of SV40 in malignant mesothelioma. [Internet] [Masters thesis]. University of Southern California; 2006. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/26565/rec/275.

Council of Science Editors:

Tomasian V. A new method to assess presence of SV40 in malignant mesothelioma. [Masters Thesis]. University of Southern California; 2006. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/26565/rec/275


University of Southern California

17. Yuksek, Kamile. Cellular proteins that interact with the hepatitis C virus F protein.

Degree: PhD, Molecular Microbiology & Immunology, 2008, University of Southern California

 Hepatitis C virus (HCV) F protein of unknown function is produced from the core protein coding region by ribosomal frameshift. It is a short lived… (more)

Subjects/Keywords: Hepatitis C Virus; F protein; proteasome subunit alpha3; hnRNPL

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APA (6th Edition):

Yuksek, K. (2008). Cellular proteins that interact with the hepatitis C virus F protein. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/99895/rec/1267

Chicago Manual of Style (16th Edition):

Yuksek, Kamile. “Cellular proteins that interact with the hepatitis C virus F protein.” 2008. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/99895/rec/1267.

MLA Handbook (7th Edition):

Yuksek, Kamile. “Cellular proteins that interact with the hepatitis C virus F protein.” 2008. Web. 21 Oct 2018.

Vancouver:

Yuksek K. Cellular proteins that interact with the hepatitis C virus F protein. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/99895/rec/1267.

Council of Science Editors:

Yuksek K. Cellular proteins that interact with the hepatitis C virus F protein. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/99895/rec/1267


University of Southern California

18. Lee, Charlene Sen-Yee. Obtaining insights into biomolecular interactions through surface plasmon resonance.

Degree: MS, Biochemistry & Molecular Biology, 2007, University of Southern California

 Surface plasmon resonance allows us to gain kinetic and equilibrium information of interactions occurring in real-time. Our biosensor instrument, BIACORE, has emerged as a powerful… (more)

Subjects/Keywords: surface plasmon resonance; biomolecular interactions; Biacore; Rev-RRE; Lyp-Csk

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APA (6th Edition):

Lee, C. S. (2007). Obtaining insights into biomolecular interactions through surface plasmon resonance. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/526716/rec/4499

Chicago Manual of Style (16th Edition):

Lee, Charlene Sen-Yee. “Obtaining insights into biomolecular interactions through surface plasmon resonance.” 2007. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/526716/rec/4499.

MLA Handbook (7th Edition):

Lee, Charlene Sen-Yee. “Obtaining insights into biomolecular interactions through surface plasmon resonance.” 2007. Web. 21 Oct 2018.

Vancouver:

Lee CS. Obtaining insights into biomolecular interactions through surface plasmon resonance. [Internet] [Masters thesis]. University of Southern California; 2007. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/526716/rec/4499.

Council of Science Editors:

Lee CS. Obtaining insights into biomolecular interactions through surface plasmon resonance. [Masters Thesis]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/526716/rec/4499


University of Southern California

19. Talwar, Sundeep. The expression of human carboxylesterases in normal tissues and cancer cell-lines.

Degree: MS, Biochemistry & Molecular Biology, 2008, University of Southern California

 Carboxylesterases (CESs) are serine esterases and are known to hydrolyze a variety of substances. CESs have been used to activate drugs that target a host… (more)

Subjects/Keywords: DNA methylation; CES expression

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APA (6th Edition):

Talwar, S. (2008). The expression of human carboxylesterases in normal tissues and cancer cell-lines. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89901/rec/6702

Chicago Manual of Style (16th Edition):

Talwar, Sundeep. “The expression of human carboxylesterases in normal tissues and cancer cell-lines.” 2008. Masters Thesis, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89901/rec/6702.

MLA Handbook (7th Edition):

Talwar, Sundeep. “The expression of human carboxylesterases in normal tissues and cancer cell-lines.” 2008. Web. 21 Oct 2018.

Vancouver:

Talwar S. The expression of human carboxylesterases in normal tissues and cancer cell-lines. [Internet] [Masters thesis]. University of Southern California; 2008. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89901/rec/6702.

Council of Science Editors:

Talwar S. The expression of human carboxylesterases in normal tissues and cancer cell-lines. [Masters Thesis]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89901/rec/6702


University of Southern California

20. Anglim, Paul P. Development of DNA methylation based biomarkers for the early detection of squamous cell lung cancer.

Degree: PhD, Biochemistry & Molecular Biology, 2008, University of Southern California

 Lung cancer is the number one cancer killer in the United States. This disease is divided into two sub-types, small cell lung cancer, (10-15% of… (more)

Subjects/Keywords: lung cancer; early detection; squamous; DNA methylation

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APA (6th Edition):

Anglim, P. P. (2008). Development of DNA methylation based biomarkers for the early detection of squamous cell lung cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/142191/rec/1931

Chicago Manual of Style (16th Edition):

Anglim, Paul P. “Development of DNA methylation based biomarkers for the early detection of squamous cell lung cancer.” 2008. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/142191/rec/1931.

MLA Handbook (7th Edition):

Anglim, Paul P. “Development of DNA methylation based biomarkers for the early detection of squamous cell lung cancer.” 2008. Web. 21 Oct 2018.

Vancouver:

Anglim PP. Development of DNA methylation based biomarkers for the early detection of squamous cell lung cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/142191/rec/1931.

Council of Science Editors:

Anglim PP. Development of DNA methylation based biomarkers for the early detection of squamous cell lung cancer. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/142191/rec/1931


University of Southern California

21. Galler, Janice Soratorio. Development of DNA methylation biomarkers as an early detection tool for human lung adenocarcinoma.

Degree: PhD, Biochemistry & Molecular Biology, 2008, University of Southern California

 Lung cancer is the leading cause of cancer-related death in the United States. It is estimated that more than 160,000 lung cancer patients will die… (more)

Subjects/Keywords: lung cancer; adenocarcinoma; DNA methylation; biomarkers; early detection

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APA (6th Edition):

Galler, J. S. (2008). Development of DNA methylation biomarkers as an early detection tool for human lung adenocarcinoma. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/117489/rec/1932

Chicago Manual of Style (16th Edition):

Galler, Janice Soratorio. “Development of DNA methylation biomarkers as an early detection tool for human lung adenocarcinoma.” 2008. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/117489/rec/1932.

MLA Handbook (7th Edition):

Galler, Janice Soratorio. “Development of DNA methylation biomarkers as an early detection tool for human lung adenocarcinoma.” 2008. Web. 21 Oct 2018.

Vancouver:

Galler JS. Development of DNA methylation biomarkers as an early detection tool for human lung adenocarcinoma. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/117489/rec/1932.

Council of Science Editors:

Galler JS. Development of DNA methylation biomarkers as an early detection tool for human lung adenocarcinoma. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/117489/rec/1932


University of Southern California

22. Ni, Min. Role of GRP78 and its novel cytosolic isoform GRP78va in regulating the unfolded protein response in cancer.

Degree: PhD, Biochemistry & Molecular Biology, 2008, University of Southern California

 The endoplasmic reticulum (ER) is an essential cellular compartment for protein synthesis and maturation and also functions as a Ca2+ storage organelle. The failure of… (more)

Subjects/Keywords: Robert Farley

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APA (6th Edition):

Ni, M. (2008). Role of GRP78 and its novel cytosolic isoform GRP78va in regulating the unfolded protein response in cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/82584/rec/5632

Chicago Manual of Style (16th Edition):

Ni, Min. “Role of GRP78 and its novel cytosolic isoform GRP78va in regulating the unfolded protein response in cancer.” 2008. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/82584/rec/5632.

MLA Handbook (7th Edition):

Ni, Min. “Role of GRP78 and its novel cytosolic isoform GRP78va in regulating the unfolded protein response in cancer.” 2008. Web. 21 Oct 2018.

Vancouver:

Ni M. Role of GRP78 and its novel cytosolic isoform GRP78va in regulating the unfolded protein response in cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/82584/rec/5632.

Council of Science Editors:

Ni M. Role of GRP78 and its novel cytosolic isoform GRP78va in regulating the unfolded protein response in cancer. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/82584/rec/5632


University of Southern California

23. Yoo, Christine Bora. Use of DNA methylation inhibitors for chemotherapy and chemoprevention of cancer.

Degree: PhD, Biochemistry & Molecular Biology, 2007, University of Southern California

 Aberrant DNA methylation is a common feature of cancer, which has been targeted for pharmacologic intervention because of its reversible nature. Nucleoside analogs such as… (more)

Subjects/Keywords: epigenetics

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APA (6th Edition):

Yoo, C. B. (2007). Use of DNA methylation inhibitors for chemotherapy and chemoprevention of cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/505277/rec/7722

Chicago Manual of Style (16th Edition):

Yoo, Christine Bora. “Use of DNA methylation inhibitors for chemotherapy and chemoprevention of cancer.” 2007. Doctoral Dissertation, University of Southern California. Accessed October 21, 2018. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/505277/rec/7722.

MLA Handbook (7th Edition):

Yoo, Christine Bora. “Use of DNA methylation inhibitors for chemotherapy and chemoprevention of cancer.” 2007. Web. 21 Oct 2018.

Vancouver:

Yoo CB. Use of DNA methylation inhibitors for chemotherapy and chemoprevention of cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2007. [cited 2018 Oct 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/505277/rec/7722.

Council of Science Editors:

Yoo CB. Use of DNA methylation inhibitors for chemotherapy and chemoprevention of cancer. [Doctoral Dissertation]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/505277/rec/7722

.