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You searched for +publisher:"University of Southern California" +contributor:("Zandi, Ebrahim"). Showing records 1 – 20 of 20 total matches.

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University of Southern California

1. Mashayekhi, Kiarash. Role of a novel transmembrane protein, TMEM56, in tumorigenic growth of human PC3 prostate cancer cell line.

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

 A novel transmembrane protein, TMEM56, was identified in Dr. Ebrahim Zandi’s lab as an IKK-β interacting protein using co-immunoprecipitation and mass spectrometry. Previous studies in… (more)

Subjects/Keywords: transmembrane proteins; TMEM56; PC3 cells; prostate cancer

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APA (6th Edition):

Mashayekhi, K. (2014). Role of a novel transmembrane protein, TMEM56, in tumorigenic growth of human PC3 prostate cancer cell line. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515438/rec/5623

Chicago Manual of Style (16th Edition):

Mashayekhi, Kiarash. “Role of a novel transmembrane protein, TMEM56, in tumorigenic growth of human PC3 prostate cancer cell line.” 2014. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515438/rec/5623.

MLA Handbook (7th Edition):

Mashayekhi, Kiarash. “Role of a novel transmembrane protein, TMEM56, in tumorigenic growth of human PC3 prostate cancer cell line.” 2014. Web. 18 Jan 2020.

Vancouver:

Mashayekhi K. Role of a novel transmembrane protein, TMEM56, in tumorigenic growth of human PC3 prostate cancer cell line. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515438/rec/5623.

Council of Science Editors:

Mashayekhi K. Role of a novel transmembrane protein, TMEM56, in tumorigenic growth of human PC3 prostate cancer cell line. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515438/rec/5623


University of Southern California

2. Li, Sicong. Mechanisms of nucleases in non-homologous DNA end joining.

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

 DNA double-stranded breaks (DSB) can occur through programmed mechanisms such as V(D)J recombination and class switch recombination or pathological mechanisms such as ionizing radiation. To… (more)

Subjects/Keywords: NHEJ; Artemis; nuclease; DNA repair

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APA (6th Edition):

Li, S. (2013). Mechanisms of nucleases in non-homologous DNA end joining. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4011

Chicago Manual of Style (16th Edition):

Li, Sicong. “Mechanisms of nucleases in non-homologous DNA end joining.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4011.

MLA Handbook (7th Edition):

Li, Sicong. “Mechanisms of nucleases in non-homologous DNA end joining.” 2013. Web. 18 Jan 2020.

Vancouver:

Li S. Mechanisms of nucleases in non-homologous DNA end joining. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4011.

Council of Science Editors:

Li S. Mechanisms of nucleases in non-homologous DNA end joining. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/342055/rec/4011


University of Southern California

3. Mo, Lijuan. De novo peptide sequencing and spectral alignment algorithm via tandem mass spectrometry.

Degree: PhD, Computational Biology & Bioinformatics, 2009, University of Southern California

 Tandem mass spectrometry (MS/MS) has become an important experimental method for high throughput proteomics based biological discovery. The most common usage of MS/MS in biological… (more)

Subjects/Keywords: tandem mass spectrometry; mass spectrometry; de novo sequencing; spectral alignment; peptide sequencing; dynamic programing

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APA (6th Edition):

Mo, L. (2009). De novo peptide sequencing and spectral alignment algorithm via tandem mass spectrometry. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266475/rec/1781

Chicago Manual of Style (16th Edition):

Mo, Lijuan. “De novo peptide sequencing and spectral alignment algorithm via tandem mass spectrometry.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266475/rec/1781.

MLA Handbook (7th Edition):

Mo, Lijuan. “De novo peptide sequencing and spectral alignment algorithm via tandem mass spectrometry.” 2009. Web. 18 Jan 2020.

Vancouver:

Mo L. De novo peptide sequencing and spectral alignment algorithm via tandem mass spectrometry. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266475/rec/1781.

Council of Science Editors:

Mo L. De novo peptide sequencing and spectral alignment algorithm via tandem mass spectrometry. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266475/rec/1781


University of Southern California

4. Wang, Ling-Chi. Mass spectrometry-based proteomic analysis of inhibitor of kappa b kinase beta and its role in cytokine-induced drug resistance in cancer.

Degree: PhD, Molecular Microbiology & Immunology, 2009, University of Southern California

 IKKbeta is the key kinase in the TNFalpha-NF-kB pathway that phosphorylates IkBalpha and targets it for polyubiquitination and degradation. As a result, NF-kB is released… (more)

Subjects/Keywords: cancer drug resistance; frit fabrication; IKK; mass spectrometry; proteomics; tumor neurosis factor

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APA (6th Edition):

Wang, L. (2009). Mass spectrometry-based proteomic analysis of inhibitor of kappa b kinase beta and its role in cytokine-induced drug resistance in cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/590663/rec/3966

Chicago Manual of Style (16th Edition):

Wang, Ling-Chi. “Mass spectrometry-based proteomic analysis of inhibitor of kappa b kinase beta and its role in cytokine-induced drug resistance in cancer.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/590663/rec/3966.

MLA Handbook (7th Edition):

Wang, Ling-Chi. “Mass spectrometry-based proteomic analysis of inhibitor of kappa b kinase beta and its role in cytokine-induced drug resistance in cancer.” 2009. Web. 18 Jan 2020.

Vancouver:

Wang L. Mass spectrometry-based proteomic analysis of inhibitor of kappa b kinase beta and its role in cytokine-induced drug resistance in cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/590663/rec/3966.

Council of Science Editors:

Wang L. Mass spectrometry-based proteomic analysis of inhibitor of kappa b kinase beta and its role in cytokine-induced drug resistance in cancer. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/590663/rec/3966


University of Southern California

5. Mesfin, Fikir. Decreased levels of expression of transmembrane protein 56 (TMEM56) in breast cancer tissues.

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

 Membrane proteins are indispensable members of the cell membrane. They anchor the cell, regulate its communication with the environment and degrade damaged cell membrane. Transmembrane… (more)

Subjects/Keywords: transmembrane protein 56; ATP synthase; laser capture microdissection; breast cancer

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APA (6th Edition):

Mesfin, F. (2014). Decreased levels of expression of transmembrane protein 56 (TMEM56) in breast cancer tissues. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458722/rec/1805

Chicago Manual of Style (16th Edition):

Mesfin, Fikir. “Decreased levels of expression of transmembrane protein 56 (TMEM56) in breast cancer tissues.” 2014. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458722/rec/1805.

MLA Handbook (7th Edition):

Mesfin, Fikir. “Decreased levels of expression of transmembrane protein 56 (TMEM56) in breast cancer tissues.” 2014. Web. 18 Jan 2020.

Vancouver:

Mesfin F. Decreased levels of expression of transmembrane protein 56 (TMEM56) in breast cancer tissues. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458722/rec/1805.

Council of Science Editors:

Mesfin F. Decreased levels of expression of transmembrane protein 56 (TMEM56) in breast cancer tissues. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/458722/rec/1805


University of Southern California

6. Qin, Lan. Histone deacetylase 4 represses matrix metalloproteinases in myofibroblastic hepatic stellate cells.

Degree: PhD, Systems Biology & Disease, 2010, University of Southern California

 It is well established that matrix metalloproteinases (MMPs) play important roles in tissue injury, cell differentiation, and cancer metastasis. In liver injury, hepatic stellate cells… (more)

Subjects/Keywords: hepatic stellate cells; histone deacetylation; matrix metalloproteinases; liver fibrosis

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APA (6th Edition):

Qin, L. (2010). Histone deacetylase 4 represses matrix metalloproteinases in myofibroblastic hepatic stellate cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/292510/rec/3192

Chicago Manual of Style (16th Edition):

Qin, Lan. “Histone deacetylase 4 represses matrix metalloproteinases in myofibroblastic hepatic stellate cells.” 2010. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/292510/rec/3192.

MLA Handbook (7th Edition):

Qin, Lan. “Histone deacetylase 4 represses matrix metalloproteinases in myofibroblastic hepatic stellate cells.” 2010. Web. 18 Jan 2020.

Vancouver:

Qin L. Histone deacetylase 4 represses matrix metalloproteinases in myofibroblastic hepatic stellate cells. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/292510/rec/3192.

Council of Science Editors:

Qin L. Histone deacetylase 4 represses matrix metalloproteinases in myofibroblastic hepatic stellate cells. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/292510/rec/3192


University of Southern California

7. Gong, Songjie. Construction and testing of chimeric antigen receptor targeting CS1 for treatment of primary effusion lymphoma.

Degree: MS, Molecular Microbiology and Immunology, 2015, University of Southern California

 Currently, no effective therapies exist for human Primary effusion Lymphoma (PEL). Here we used a humanized CS1 monoclonal antibody (mAb) to target CS1, which is… (more)

Subjects/Keywords: primary effusion lymphoma; multiple myeloma; chimeric antigen receptor; CS1

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APA (6th Edition):

Gong, S. (2015). Construction and testing of chimeric antigen receptor targeting CS1 for treatment of primary effusion lymphoma. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615523/rec/1605

Chicago Manual of Style (16th Edition):

Gong, Songjie. “Construction and testing of chimeric antigen receptor targeting CS1 for treatment of primary effusion lymphoma.” 2015. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615523/rec/1605.

MLA Handbook (7th Edition):

Gong, Songjie. “Construction and testing of chimeric antigen receptor targeting CS1 for treatment of primary effusion lymphoma.” 2015. Web. 18 Jan 2020.

Vancouver:

Gong S. Construction and testing of chimeric antigen receptor targeting CS1 for treatment of primary effusion lymphoma. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615523/rec/1605.

Council of Science Editors:

Gong S. Construction and testing of chimeric antigen receptor targeting CS1 for treatment of primary effusion lymphoma. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615523/rec/1605


University of Southern California

8. Hong, Dai. Studies on the role of a novel protein, TMEM 56 in tumorigenic growth for MCF-7 cells.

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

 Transmembrane protein TMEM 56 was first identified as an IKK‐associated protein by mass spectrometry in Dr. Ebrahim Zandi’s lab. This 263AA protein was found to… (more)

Subjects/Keywords: protein; TMEM 56; tumorigenic growth; MCF-7 cells

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APA (6th Edition):

Hong, D. (2014). Studies on the role of a novel protein, TMEM 56 in tumorigenic growth for MCF-7 cells. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/404283/rec/6174

Chicago Manual of Style (16th Edition):

Hong, Dai. “Studies on the role of a novel protein, TMEM 56 in tumorigenic growth for MCF-7 cells.” 2014. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/404283/rec/6174.

MLA Handbook (7th Edition):

Hong, Dai. “Studies on the role of a novel protein, TMEM 56 in tumorigenic growth for MCF-7 cells.” 2014. Web. 18 Jan 2020.

Vancouver:

Hong D. Studies on the role of a novel protein, TMEM 56 in tumorigenic growth for MCF-7 cells. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/404283/rec/6174.

Council of Science Editors:

Hong D. Studies on the role of a novel protein, TMEM 56 in tumorigenic growth for MCF-7 cells. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/404283/rec/6174


University of Southern California

9. Le, Anh-Huy Phan. The importance of Dfp1 in alkylation damage response and meiosis.

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

 In Schizosaccharomyces pombe, the DDK complex is a conserved, essential kinase complex consisting of a catalytic subunit, Hsk1 (Cdc7), and its regulatory subunit Dfp1 (Dbf4).… (more)

Subjects/Keywords: alkylation damage; DDK; Dfp1; Hsk1; meiosis; S. Pombe

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APA (6th Edition):

Le, A. P. (2011). The importance of Dfp1 in alkylation damage response and meiosis. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856

Chicago Manual of Style (16th Edition):

Le, Anh-Huy Phan. “The importance of Dfp1 in alkylation damage response and meiosis.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856.

MLA Handbook (7th Edition):

Le, Anh-Huy Phan. “The importance of Dfp1 in alkylation damage response and meiosis.” 2011. Web. 18 Jan 2020.

Vancouver:

Le AP. The importance of Dfp1 in alkylation damage response and meiosis. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856.

Council of Science Editors:

Le AP. The importance of Dfp1 in alkylation damage response and meiosis. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/666811/rec/6856


University of Southern California

10. Reilly-Rhoten, Heather Noelle. Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM.

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

 The importance of histones for DNA management cannot be understated. From rearrangement to regulation of expression, histones act as the principle effectors of DNA availability… (more)

Subjects/Keywords: mass spectrometry; histones; post-translational modifications

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APA (6th Edition):

Reilly-Rhoten, H. N. (2012). Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3309

Chicago Manual of Style (16th Edition):

Reilly-Rhoten, Heather Noelle. “Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM.” 2012. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3309.

MLA Handbook (7th Edition):

Reilly-Rhoten, Heather Noelle. “Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM.” 2012. Web. 18 Jan 2020.

Vancouver:

Reilly-Rhoten HN. Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3309.

Council of Science Editors:

Reilly-Rhoten HN. Identification and characterization of post-translational modifications on histones: an on-line top-down mass spectrometry workflow for analysis using ProSight PTM. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8330/rec/3309


University of Southern California

11. Wei, Hsiao-Fan. Studies on the expression and function of the human TMEM56 protein.

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

 Transmembrane 56 (TMEM56) is a 30 KDa protein and it is highly conserved in most species. The protein was identified as an IKKβ-interacting protein by… (more)

Subjects/Keywords: ATP synthease enzyme activity assay; LTQ-ETD; mitochondria; TMEM56; transmembrane protein; western blotting

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APA (6th Edition):

Wei, H. (2011). Studies on the expression and function of the human TMEM56 protein. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/615287/rec/6171

Chicago Manual of Style (16th Edition):

Wei, Hsiao-Fan. “Studies on the expression and function of the human TMEM56 protein.” 2011. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/615287/rec/6171.

MLA Handbook (7th Edition):

Wei, Hsiao-Fan. “Studies on the expression and function of the human TMEM56 protein.” 2011. Web. 18 Jan 2020.

Vancouver:

Wei H. Studies on the expression and function of the human TMEM56 protein. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/615287/rec/6171.

Council of Science Editors:

Wei H. Studies on the expression and function of the human TMEM56 protein. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/615287/rec/6171


University of Southern California

12. Kuo, Wan-I. Snake venom proteins identification by nano high performance liquid chromatography tandem mass spectrometry.

Degree: MS, Biochemistry & Molecular Biology, 2009, University of Southern California

 In this study, a modified on-column frit preparation method for fused silica capillaries was used to analyze a venom mixture which contained the milkings from… (more)

Subjects/Keywords: Agkistrodon contortrix contortrix; mass spectrometry; proteomics; snake venomics

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APA (6th Edition):

Kuo, W. (2009). Snake venom proteins identification by nano high performance liquid chromatography tandem mass spectrometry. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/270646/rec/5896

Chicago Manual of Style (16th Edition):

Kuo, Wan-I. “Snake venom proteins identification by nano high performance liquid chromatography tandem mass spectrometry.” 2009. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/270646/rec/5896.

MLA Handbook (7th Edition):

Kuo, Wan-I. “Snake venom proteins identification by nano high performance liquid chromatography tandem mass spectrometry.” 2009. Web. 18 Jan 2020.

Vancouver:

Kuo W. Snake venom proteins identification by nano high performance liquid chromatography tandem mass spectrometry. [Internet] [Masters thesis]. University of Southern California; 2009. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/270646/rec/5896.

Council of Science Editors:

Kuo W. Snake venom proteins identification by nano high performance liquid chromatography tandem mass spectrometry. [Masters Thesis]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/270646/rec/5896


University of Southern California

13. Roy, Deepankar. The mechanism of R-loop formation in mammalian immunoglobulin class switch recombination.

Degree: PhD, Biochemistry & Molecular Biology, 2009, University of Southern California

 R-loops form at immunoglobulin (Ig) heavy chain locus in germinal center B-cells undergoing class switch recombination (CSR). These are triple-stranded structures formed upon transcription of… (more)

Subjects/Keywords: antibody class switch recombination; R-loop; RNA:DNA hybrid; isotype switch; RNA polymerase; transcription; thermodynamic stability; nucleic acid; G-cluster; G-quartet; template; nontemplate strand; RNA threadback

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APA (6th Edition):

Roy, D. (2009). The mechanism of R-loop formation in mammalian immunoglobulin class switch recombination. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/244005/rec/6974

Chicago Manual of Style (16th Edition):

Roy, Deepankar. “The mechanism of R-loop formation in mammalian immunoglobulin class switch recombination.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/244005/rec/6974.

MLA Handbook (7th Edition):

Roy, Deepankar. “The mechanism of R-loop formation in mammalian immunoglobulin class switch recombination.” 2009. Web. 18 Jan 2020.

Vancouver:

Roy D. The mechanism of R-loop formation in mammalian immunoglobulin class switch recombination. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/244005/rec/6974.

Council of Science Editors:

Roy D. The mechanism of R-loop formation in mammalian immunoglobulin class switch recombination. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/244005/rec/6974


University of Southern California

14. Xu, Shili. Discovery of novel small molecules for ovarian cancer treatment.

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

 Ovarian cancer is one of the leading cancers causing women’s death in the United States mainly due to its late diagnosis and resistance to current… (more)

Subjects/Keywords: ovarian cancer; protein disulfide isomerase (PDI); propynoic acid carbamoyl methyl amide (PACMA); PACMA 31; ER stress; unfolded protein response (UPR); glycoprotein 130 (gp130); SC144; small molecule; chemotherapy; drug resistance; inhibitor; quinoxalinhydrazide; xenograft; oral bioavailability; Stat3

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APA (6th Edition):

Xu, S. (2013). Discovery of novel small molecules for ovarian cancer treatment. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2026

Chicago Manual of Style (16th Edition):

Xu, Shili. “Discovery of novel small molecules for ovarian cancer treatment.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2026.

MLA Handbook (7th Edition):

Xu, Shili. “Discovery of novel small molecules for ovarian cancer treatment.” 2013. Web. 18 Jan 2020.

Vancouver:

Xu S. Discovery of novel small molecules for ovarian cancer treatment. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2026.

Council of Science Editors:

Xu S. Discovery of novel small molecules for ovarian cancer treatment. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2026


University of Southern California

15. Millard, Melissa. Discovery of novel small molecules targeting cancer cell metabolism.

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

 Advanced age is a risk-factor common to most cancers. In coming years, a marked increase in the population aged 65 and over will compound the… (more)

Subjects/Keywords: small molecule anti-cancer agents; pancreatic cancer; breast cancer; mitochondria; cancer cell metabolism; PKM2; pyruvate kinase M2; oncology; cancer therapy

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

APA (6th Edition):

Millard, M. (2013). Discovery of novel small molecules targeting cancer cell metabolism. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027

Chicago Manual of Style (16th Edition):

Millard, Melissa. “Discovery of novel small molecules targeting cancer cell metabolism.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027.

MLA Handbook (7th Edition):

Millard, Melissa. “Discovery of novel small molecules targeting cancer cell metabolism.” 2013. Web. 18 Jan 2020.

Vancouver:

Millard M. Discovery of novel small molecules targeting cancer cell metabolism. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027.

Council of Science Editors:

Millard M. Discovery of novel small molecules targeting cancer cell metabolism. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2027


University of Southern California

16. Geary, Lauren Alexandra Rios. Role of cancer-associated fibroblast secreted annexin A1 in generation and maintenance of prostate cancer stem cells.

Degree: PhD, Integrative Biology of Disease, 2014, University of Southern California

 Annexin A1 (AnxA1), a phospholipid-binding protein and known regulator of glucocorticoid-induced inflammatory signaling, has been implicated for its role in human cancers, including head and… (more)

Subjects/Keywords: adenocarcinoma; annexin A1; cancer stem cells; EMT; prostate cancer

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APA (6th Edition):

Geary, L. A. R. (2014). Role of cancer-associated fibroblast secreted annexin A1 in generation and maintenance of prostate cancer stem cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/327884/rec/5626

Chicago Manual of Style (16th Edition):

Geary, Lauren Alexandra Rios. “Role of cancer-associated fibroblast secreted annexin A1 in generation and maintenance of prostate cancer stem cells.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/327884/rec/5626.

MLA Handbook (7th Edition):

Geary, Lauren Alexandra Rios. “Role of cancer-associated fibroblast secreted annexin A1 in generation and maintenance of prostate cancer stem cells.” 2014. Web. 18 Jan 2020.

Vancouver:

Geary LAR. Role of cancer-associated fibroblast secreted annexin A1 in generation and maintenance of prostate cancer stem cells. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/327884/rec/5626.

Council of Science Editors:

Geary LAR. Role of cancer-associated fibroblast secreted annexin A1 in generation and maintenance of prostate cancer stem cells. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/327884/rec/5626


University of Southern California

17. Shabaik, Yumna Hosam. Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy.

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

 Pancreatic cancer is one of the deadliest cancers with a 5-year survival rate of 6%. Therapeutic options against this disease are limited and there is… (more)

Subjects/Keywords: cancer; mitochondria; small molecule; triphenylphosphonium cation

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

APA (6th Edition):

Shabaik, Y. H. (2013). Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1953

Chicago Manual of Style (16th Edition):

Shabaik, Yumna Hosam. “Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1953.

MLA Handbook (7th Edition):

Shabaik, Yumna Hosam. “Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy.” 2013. Web. 18 Jan 2020.

Vancouver:

Shabaik YH. Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1953.

Council of Science Editors:

Shabaik YH. Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1953


University of Southern California

18. Murali, Poornima. Role of a novel transmembrane protein, MTTS1 in mitochondrial regulation and tumor suppression.

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

 A novel transmembrane protein was identified in Dr. Ebrahim Zandi’s lab as an IKK-β interacting protein by mass spectrometry. Mass spectrometry and IP (Immunoprecipitation) studies… (more)

Subjects/Keywords: cancer; tumor supression; transmembrane protein; mitochondrial abundance

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APA (6th Edition):

Murali, P. (2014). Role of a novel transmembrane protein, MTTS1 in mitochondrial regulation and tumor suppression. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/86121/rec/5622

Chicago Manual of Style (16th Edition):

Murali, Poornima. “Role of a novel transmembrane protein, MTTS1 in mitochondrial regulation and tumor suppression.” 2014. Masters Thesis, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/86121/rec/5622.

MLA Handbook (7th Edition):

Murali, Poornima. “Role of a novel transmembrane protein, MTTS1 in mitochondrial regulation and tumor suppression.” 2014. Web. 18 Jan 2020.

Vancouver:

Murali P. Role of a novel transmembrane protein, MTTS1 in mitochondrial regulation and tumor suppression. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/86121/rec/5622.

Council of Science Editors:

Murali P. Role of a novel transmembrane protein, MTTS1 in mitochondrial regulation and tumor suppression. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/86121/rec/5622


University of Southern California

19. Gu, Jiafeng. Mechanism of human nonhomologous DNA end joining.

Degree: PhD, Molecular Biology, 2009, University of Southern California

 DNA double-strand breaks (DSBs) represent the most deleterious form of DNA damage, as both of the DNA strands are broken. In mammalian cells, DSBs are… (more)

Subjects/Keywords: biochemical reconstitution; cancer treatment; DNA double strand break; DNA repair and recombination; nonhomologous DNA end joining

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

APA (6th Edition):

Gu, J. (2009). Mechanism of human nonhomologous DNA end joining. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/407480/rec/4003

Chicago Manual of Style (16th Edition):

Gu, Jiafeng. “Mechanism of human nonhomologous DNA end joining.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/407480/rec/4003.

MLA Handbook (7th Edition):

Gu, Jiafeng. “Mechanism of human nonhomologous DNA end joining.” 2009. Web. 18 Jan 2020.

Vancouver:

Gu J. Mechanism of human nonhomologous DNA end joining. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/407480/rec/4003.

Council of Science Editors:

Gu J. Mechanism of human nonhomologous DNA end joining. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/407480/rec/4003


University of Southern California

20. Lu, Haihui. Biochemistry and reconstitution of V(D)J recombination in a purified system.

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

 Evolved from invertebrate transposons, V(D)J recombination is the vertebrate gene rearrangement process for assembling the antigen receptor genes, which encode immunoglobulins and T cell receptors.… (more)

Subjects/Keywords: VDJ recombination; reconstitution; RAG; Artemis; DNA-PKcs; NHEJ

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

APA (6th Edition):

Lu, H. (2008). Biochemistry and reconstitution of V(D)J recombination in a purified system. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/49964/rec/1108

Chicago Manual of Style (16th Edition):

Lu, Haihui. “Biochemistry and reconstitution of V(D)J recombination in a purified system.” 2008. Doctoral Dissertation, University of Southern California. Accessed January 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/49964/rec/1108.

MLA Handbook (7th Edition):

Lu, Haihui. “Biochemistry and reconstitution of V(D)J recombination in a purified system.” 2008. Web. 18 Jan 2020.

Vancouver:

Lu H. Biochemistry and reconstitution of V(D)J recombination in a purified system. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Jan 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/49964/rec/1108.

Council of Science Editors:

Lu H. Biochemistry and reconstitution of V(D)J recombination in a purified system. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/49964/rec/1108

.