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You searched for +publisher:"University of Southern California" +contributor:("Rice, Judd C."). Showing records 1 – 28 of 28 total matches.

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University of Southern California

1. Nugent, Rebecca Lynn. The S. pombe Mst1 histone acetyltransferase is required for genome stability.

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

 Within the cell DNA exists as chromatin, a complex mass of nucleic acids and proteins. Chromatin is highly structured and is compacted through the interaction… (more)

Subjects/Keywords: Mst1; MYST; fission yeast; genome stability; histone acetyltransferase; chromatin; centromere; DNA damage repair; transcription

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APA (6th Edition):

Nugent, R. L. (2010). The S. pombe Mst1 histone acetyltransferase is required for genome stability. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/380147/rec/7279

Chicago Manual of Style (16th Edition):

Nugent, Rebecca Lynn. “The S. pombe Mst1 histone acetyltransferase is required for genome stability.” 2010. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/380147/rec/7279.

MLA Handbook (7th Edition):

Nugent, Rebecca Lynn. “The S. pombe Mst1 histone acetyltransferase is required for genome stability.” 2010. Web. 22 Jan 2020.

Vancouver:

Nugent RL. The S. pombe Mst1 histone acetyltransferase is required for genome stability. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/380147/rec/7279.

Council of Science Editors:

Nugent RL. The S. pombe Mst1 histone acetyltransferase is required for genome stability. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/380147/rec/7279


University of Southern California

2. Ianculescu, Irina. One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2011, University of Southern California

 It is becoming increasingly evident that transcriptional coregulators are a diverse group of proteins of central importance to gene expression. Although some appear to be… (more)

Subjects/Keywords: transcriptional regulation; nuclear receptor coactivators; p300/CBP

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APA (6th Edition):

Ianculescu, I. (2011). One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561

Chicago Manual of Style (16th Edition):

Ianculescu, Irina. “One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561.

MLA Handbook (7th Edition):

Ianculescu, Irina. “One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription.” 2011. Web. 22 Jan 2020.

Vancouver:

Ianculescu I. One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561.

Council of Science Editors:

Ianculescu I. One play, many actors: the many roles coregulators play in nuclear receptor mediated transcription. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/175732/rec/4561


University of Southern California

3. Yates, Peter Christian. The histone H2A deubiquitinase MYSM1 regulates CCR9 expression on CD4⁺ T cells and thymocytes.

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

 Directed cellular migration, also known as homing, is the hallmark of an efficient and effective immune system. Not only is cellular migration a necessary requirement… (more)

Subjects/Keywords: CCR9; MYSM1; deubiquitinase; trafficking

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APA (6th Edition):

Yates, P. C. (2013). The histone H2A deubiquitinase MYSM1 regulates CCR9 expression on CD4⁺ T cells and thymocytes. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/345310/rec/6758

Chicago Manual of Style (16th Edition):

Yates, Peter Christian. “The histone H2A deubiquitinase MYSM1 regulates CCR9 expression on CD4⁺ T cells and thymocytes.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/345310/rec/6758.

MLA Handbook (7th Edition):

Yates, Peter Christian. “The histone H2A deubiquitinase MYSM1 regulates CCR9 expression on CD4⁺ T cells and thymocytes.” 2013. Web. 22 Jan 2020.

Vancouver:

Yates PC. The histone H2A deubiquitinase MYSM1 regulates CCR9 expression on CD4⁺ T cells and thymocytes. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/345310/rec/6758.

Council of Science Editors:

Yates PC. The histone H2A deubiquitinase MYSM1 regulates CCR9 expression on CD4⁺ T cells and thymocytes. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/345310/rec/6758


University of Southern California

4. Hu, Yixin. Impacts of post-translational modifications on interactions between G9a and its N-terminus binding partners.

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

 Nuclear receptors regulate transcription of target genes with the help of numerous coregulators, including G9a. G9a is well known as a histone methyltransferase and a… (more)

Subjects/Keywords: nuclear receptors; G9a; heterochromatin protein 1γ

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APA (6th Edition):

Hu, Y. (2015). Impacts of post-translational modifications on interactions between G9a and its N-terminus binding partners. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595843/rec/3378

Chicago Manual of Style (16th Edition):

Hu, Yixin. “Impacts of post-translational modifications on interactions between G9a and its N-terminus binding partners.” 2015. Masters Thesis, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595843/rec/3378.

MLA Handbook (7th Edition):

Hu, Yixin. “Impacts of post-translational modifications on interactions between G9a and its N-terminus binding partners.” 2015. Web. 22 Jan 2020.

Vancouver:

Hu Y. Impacts of post-translational modifications on interactions between G9a and its N-terminus binding partners. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595843/rec/3378.

Council of Science Editors:

Hu Y. Impacts of post-translational modifications on interactions between G9a and its N-terminus binding partners. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595843/rec/3378


University of Southern California

5. Spektor, Tanya Magazinnik. Identification and characterization of PR-Set7 and histone H4 lysine 20 methylation-associated proteins.

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

 Chromatin is the complex of DNA, histones, and nonhistone proteins found in the nucleus of a eukaryotic cell and is known to play a critical… (more)

Subjects/Keywords: chromatin; epigenetics; histone methylation; histone H4 lysine 20; sumoylation; DNA repair; Ku70/80; PARP1; PR-Set7; UBC9; mammalian tethered-catalysis (MTeC); methyl-binding proteins

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APA (6th Edition):

Spektor, T. M. (2009). Identification and characterization of PR-Set7 and histone H4 lysine 20 methylation-associated proteins. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/280858/rec/3310

Chicago Manual of Style (16th Edition):

Spektor, Tanya Magazinnik. “Identification and characterization of PR-Set7 and histone H4 lysine 20 methylation-associated proteins.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/280858/rec/3310.

MLA Handbook (7th Edition):

Spektor, Tanya Magazinnik. “Identification and characterization of PR-Set7 and histone H4 lysine 20 methylation-associated proteins.” 2009. Web. 22 Jan 2020.

Vancouver:

Spektor TM. Identification and characterization of PR-Set7 and histone H4 lysine 20 methylation-associated proteins. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/280858/rec/3310.

Council of Science Editors:

Spektor TM. Identification and characterization of PR-Set7 and histone H4 lysine 20 methylation-associated proteins. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/280858/rec/3310


University of Southern California

6. Erceg, David Ned James. The effects of whole body vibration exercise on metabolic systems in overweight Latino boys.

Degree: PhD, Biokinesiology, 2011, University of Southern California

 With an increasing childhood obesity epidemic, efficient methods of exercise are sought to improve health. Vibration training has been in use for decades to improve… (more)

Subjects/Keywords: vibration; insulin resistance; bone

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APA (6th Edition):

Erceg, D. N. J. (2011). The effects of whole body vibration exercise on metabolic systems in overweight Latino boys. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/645321/rec/6670

Chicago Manual of Style (16th Edition):

Erceg, David Ned James. “The effects of whole body vibration exercise on metabolic systems in overweight Latino boys.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/645321/rec/6670.

MLA Handbook (7th Edition):

Erceg, David Ned James. “The effects of whole body vibration exercise on metabolic systems in overweight Latino boys.” 2011. Web. 22 Jan 2020.

Vancouver:

Erceg DNJ. The effects of whole body vibration exercise on metabolic systems in overweight Latino boys. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/645321/rec/6670.

Council of Science Editors:

Erceg DNJ. The effects of whole body vibration exercise on metabolic systems in overweight Latino boys. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/645321/rec/6670


University of Southern California

7. Butuči, Melina. Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells.

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

 During early development in many animals, embryonic cells transition from periods of transcriptional quiescence to abrupt activation of RNA polymerase II (RNAPII)‐dependent transcription on a… (more)

Subjects/Keywords: C. elegans; primordial germ cells; PGC; Z2/Z3; DNA damage; transcription; X chromosome; TOPOII

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APA (6th Edition):

Butuči, M. (2015). Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988

Chicago Manual of Style (16th Edition):

Butuči, Melina. “Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells.” 2015. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988.

MLA Handbook (7th Edition):

Butuči, Melina. “Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells.” 2015. Web. 22 Jan 2020.

Vancouver:

Butuči M. Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988.

Council of Science Editors:

Butuči M. Zygotic genome activation triggers chromosome damage and checkpoint signaling in Caenorhabditis elegans primordial germ cells. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/637935/rec/7988


University of Southern California

8. Hughes, Michael Warren. Epigenetic and genetic reprogramming during embryonic chicken feather bud morphogenesis, hair morphogenesis, and de novo hair regeneration.

Degree: PhD, Pathobiology, 2012, University of Southern California

 The ability to engineer a tissue to replace diseased organs is a goal that when achieved will provide an incredible asset to clinicians. In order… (more)

Subjects/Keywords: stem cell; epigenetic; hair; feather bud; embryonic; morphogenesis; competence; de novo; regeneration; reprogramming; histone

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APA (6th Edition):

Hughes, M. W. (2012). Epigenetic and genetic reprogramming during embryonic chicken feather bud morphogenesis, hair morphogenesis, and de novo hair regeneration. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/14427/rec/2408

Chicago Manual of Style (16th Edition):

Hughes, Michael Warren. “Epigenetic and genetic reprogramming during embryonic chicken feather bud morphogenesis, hair morphogenesis, and de novo hair regeneration.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/14427/rec/2408.

MLA Handbook (7th Edition):

Hughes, Michael Warren. “Epigenetic and genetic reprogramming during embryonic chicken feather bud morphogenesis, hair morphogenesis, and de novo hair regeneration.” 2012. Web. 22 Jan 2020.

Vancouver:

Hughes MW. Epigenetic and genetic reprogramming during embryonic chicken feather bud morphogenesis, hair morphogenesis, and de novo hair regeneration. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/14427/rec/2408.

Council of Science Editors:

Hughes MW. Epigenetic and genetic reprogramming during embryonic chicken feather bud morphogenesis, hair morphogenesis, and de novo hair regeneration. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/14427/rec/2408


University of Southern California

9. Hinoue, Toshinori. DNA hypermethylation: its role in colorectal tumorigenesis and potential clinical applications.

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

 Aberrant DNA hypermethylation of CpG islands is a common and early event in colorectal tumorigenesis. Promoter DNA hypermethylation is associated with transcriptional gene silencing, and… (more)

Subjects/Keywords: colorectal cancer; DNA methylation; CIMP

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APA (6th Edition):

Hinoue, T. (2011). DNA hypermethylation: its role in colorectal tumorigenesis and potential clinical applications. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/238424/rec/2063

Chicago Manual of Style (16th Edition):

Hinoue, Toshinori. “DNA hypermethylation: its role in colorectal tumorigenesis and potential clinical applications.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/238424/rec/2063.

MLA Handbook (7th Edition):

Hinoue, Toshinori. “DNA hypermethylation: its role in colorectal tumorigenesis and potential clinical applications.” 2011. Web. 22 Jan 2020.

Vancouver:

Hinoue T. DNA hypermethylation: its role in colorectal tumorigenesis and potential clinical applications. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/238424/rec/2063.

Council of Science Editors:

Hinoue T. DNA hypermethylation: its role in colorectal tumorigenesis and potential clinical applications. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/238424/rec/2063


University of Southern California

10. Sims, Jennifer Kae. The role of histone H4 lysine 20 monomethylation in gene expression and differentiation.

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

 In developing multi-cellular organisms, cell fate decisions are largely determined by epigenetic programs that activate and repress specific sets of genes. For eukaryotic gene regulation,… (more)

Subjects/Keywords: histone H4 lysine 20; gene expression; differentiation

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APA (6th Edition):

Sims, J. K. (2010). The role of histone H4 lysine 20 monomethylation in gene expression and differentiation. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/88881/rec/7224

Chicago Manual of Style (16th Edition):

Sims, Jennifer Kae. “The role of histone H4 lysine 20 monomethylation in gene expression and differentiation.” 2010. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/88881/rec/7224.

MLA Handbook (7th Edition):

Sims, Jennifer Kae. “The role of histone H4 lysine 20 monomethylation in gene expression and differentiation.” 2010. Web. 22 Jan 2020.

Vancouver:

Sims JK. The role of histone H4 lysine 20 monomethylation in gene expression and differentiation. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/88881/rec/7224.

Council of Science Editors:

Sims JK. The role of histone H4 lysine 20 monomethylation in gene expression and differentiation. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/88881/rec/7224


University of Southern California

11. Houston, Sabrina Ishimaru. Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome.

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

 The post-translational modification of histones is thought to play a critical role in directing nuclear events involving chromatin. One such modification, Histone H4 Lysine 20… (more)

Subjects/Keywords: epigenetics; histone methylation

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APA (6th Edition):

Houston, S. I. (2009). Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6162

Chicago Manual of Style (16th Edition):

Houston, Sabrina Ishimaru. “Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6162.

MLA Handbook (7th Edition):

Houston, Sabrina Ishimaru. “Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome.” 2009. Web. 22 Jan 2020.

Vancouver:

Houston SI. Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6162.

Council of Science Editors:

Houston SI. Studies of the biological relevance of Histone H4 Lysine 20 monomethylation: discovery of its role in the cell cycle and localization within the human genome. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/558150/rec/6162


University of Southern California

12. Lee, Janet M. The mechanism of recruitment of Tip60 to ER target genes.

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

 The steroid receptors in the nuclear receptor superfamily are responsible for regulating many different functions including transcription. However, in order to completely and correctly activate… (more)

Subjects/Keywords: Tip60; coactivator; nuclear receptor

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APA (6th Edition):

Lee, J. M. (2011). The mechanism of recruitment of Tip60 to ER target genes. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/441052/rec/6975

Chicago Manual of Style (16th Edition):

Lee, Janet M. “The mechanism of recruitment of Tip60 to ER target genes.” 2011. Masters Thesis, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/441052/rec/6975.

MLA Handbook (7th Edition):

Lee, Janet M. “The mechanism of recruitment of Tip60 to ER target genes.” 2011. Web. 22 Jan 2020.

Vancouver:

Lee JM. The mechanism of recruitment of Tip60 to ER target genes. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/441052/rec/6975.

Council of Science Editors:

Lee JM. The mechanism of recruitment of Tip60 to ER target genes. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/441052/rec/6975


University of Southern California

13. Dieli-Conwright, Christina M. Influence of hormone replacement therapy with maximal eccentric exercise on estrogen receptor coregulators and skeletal muscle damage in postmenopausal women.

Degree: PhD, Biokinesiology & Physical Therapy, 2009, University of Southern California

 The use of hormone replacement therapy (HRT) is a potential treatment to relieve symptoms of menopause and prevent the onset of disease such as osteoporosis… (more)

Subjects/Keywords: skeletal muscle; resistance exercise; estrogen

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APA (6th Edition):

Dieli-Conwright, C. M. (2009). Influence of hormone replacement therapy with maximal eccentric exercise on estrogen receptor coregulators and skeletal muscle damage in postmenopausal women. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/218682/rec/3480

Chicago Manual of Style (16th Edition):

Dieli-Conwright, Christina M. “Influence of hormone replacement therapy with maximal eccentric exercise on estrogen receptor coregulators and skeletal muscle damage in postmenopausal women.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/218682/rec/3480.

MLA Handbook (7th Edition):

Dieli-Conwright, Christina M. “Influence of hormone replacement therapy with maximal eccentric exercise on estrogen receptor coregulators and skeletal muscle damage in postmenopausal women.” 2009. Web. 22 Jan 2020.

Vancouver:

Dieli-Conwright CM. Influence of hormone replacement therapy with maximal eccentric exercise on estrogen receptor coregulators and skeletal muscle damage in postmenopausal women. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/218682/rec/3480.

Council of Science Editors:

Dieli-Conwright CM. Influence of hormone replacement therapy with maximal eccentric exercise on estrogen receptor coregulators and skeletal muscle damage in postmenopausal women. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/218682/rec/3480


University of Southern California

14. Wu, Brian Wen-Long. Investigations into causes of muscle atrophy and improving clinical outcomes following lower limb surgeries.

Degree: PhD, Integrative Biology of Disease, 2015, University of Southern California

 Muscle atrophy is a major impediment to rehabilitation and continues to have billions of research dollars spent annually on the topic. Orthopedic surgery is a… (more)

Subjects/Keywords: muscle atrophy; testosterone; lower limb surgeries; tourniquet

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APA (6th Edition):

Wu, B. W. (2015). Investigations into causes of muscle atrophy and improving clinical outcomes following lower limb surgeries. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595160/rec/3653

Chicago Manual of Style (16th Edition):

Wu, Brian Wen-Long. “Investigations into causes of muscle atrophy and improving clinical outcomes following lower limb surgeries.” 2015. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595160/rec/3653.

MLA Handbook (7th Edition):

Wu, Brian Wen-Long. “Investigations into causes of muscle atrophy and improving clinical outcomes following lower limb surgeries.” 2015. Web. 22 Jan 2020.

Vancouver:

Wu BW. Investigations into causes of muscle atrophy and improving clinical outcomes following lower limb surgeries. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595160/rec/3653.

Council of Science Editors:

Wu BW. Investigations into causes of muscle atrophy and improving clinical outcomes following lower limb surgeries. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595160/rec/3653


University of Southern California

15. Li, Pao-Chen. The centromere: replication, recombination, reassembly.

Degree: PhD, Molecular Biology, 2012, University of Southern California

 Normal cell division requires faithful DNA replication and proper DNA segregation in order to generate two identical daughter cells. Within cells DNA is always assembled… (more)

Subjects/Keywords: centromere; replication; heterochromatin; recombination; chromosome segregation; hp1; swi6; cdc6; rad51

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APA (6th Edition):

Li, P. (2012). The centromere: replication, recombination, reassembly. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/213298/rec/6487

Chicago Manual of Style (16th Edition):

Li, Pao-Chen. “The centromere: replication, recombination, reassembly.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/213298/rec/6487.

MLA Handbook (7th Edition):

Li, Pao-Chen. “The centromere: replication, recombination, reassembly.” 2012. Web. 22 Jan 2020.

Vancouver:

Li P. The centromere: replication, recombination, reassembly. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/213298/rec/6487.

Council of Science Editors:

Li P. The centromere: replication, recombination, reassembly. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/213298/rec/6487


University of Southern California

16. Zhong, Yuan. The role of Cdc7 in replication fork progression in response to DNA damage.

Degree: PhD, Molecular Biology, 2012, University of Southern California

 Cdc7-Dbf4 is an essential protein kinase complex required for every single origin firing. As a target of the intra-S checkpoint, Cdc7 kinase activity has also… (more)

Subjects/Keywords: Cdc7; replication fork; DNA damage; fork progression; MMS

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APA (6th Edition):

Zhong, Y. (2012). The role of Cdc7 in replication fork progression in response to DNA damage. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199

Chicago Manual of Style (16th Edition):

Zhong, Yuan. “The role of Cdc7 in replication fork progression in response to DNA damage.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199.

MLA Handbook (7th Edition):

Zhong, Yuan. “The role of Cdc7 in replication fork progression in response to DNA damage.” 2012. Web. 22 Jan 2020.

Vancouver:

Zhong Y. The role of Cdc7 in replication fork progression in response to DNA damage. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199.

Council of Science Editors:

Zhong Y. The role of Cdc7 in replication fork progression in response to DNA damage. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/18011/rec/7199


University of Southern California

17. Congdon, Lauren Marie. Multiple functions of the PR-Set7 histone methyltransferase: from transcription to the cell cycle.

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

 Within the eukaryotic nucleus, DNA is packaged via its interaction with histones and non-histone proteins into a structure known as chromatin. Chromatin is dynamic in… (more)

Subjects/Keywords: histone code; histone methylation; PR-Set7; Riz1; transcription

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APA (6th Edition):

Congdon, L. M. (2012). Multiple functions of the PR-Set7 histone methyltransferase: from transcription to the cell cycle. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110854/rec/4269

Chicago Manual of Style (16th Edition):

Congdon, Lauren Marie. “Multiple functions of the PR-Set7 histone methyltransferase: from transcription to the cell cycle.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110854/rec/4269.

MLA Handbook (7th Edition):

Congdon, Lauren Marie. “Multiple functions of the PR-Set7 histone methyltransferase: from transcription to the cell cycle.” 2012. Web. 22 Jan 2020.

Vancouver:

Congdon LM. Multiple functions of the PR-Set7 histone methyltransferase: from transcription to the cell cycle. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110854/rec/4269.

Council of Science Editors:

Congdon LM. Multiple functions of the PR-Set7 histone methyltransferase: from transcription to the cell cycle. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110854/rec/4269


University of Southern California

18. Veerappan, Chendhore Sai. Epigenetic plasticity of cultured female human embryonic stem cells and regulation of gene expression and chromatin by PR-SET7 mediated H4K20me1.

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

 Epigenetics is the study of changes in gene expression that occur in cells without alterations to DNA sequence. Epigenetic modifications are critical components of eukaryotic… (more)

Subjects/Keywords: epigenetics; embryonic stem cells; X-chromosome inactivation; H4K4me3; H3K27me3; heterogeneity

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APA (6th Edition):

Veerappan, C. S. (2012). Epigenetic plasticity of cultured female human embryonic stem cells and regulation of gene expression and chromatin by PR-SET7 mediated H4K20me1. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112300/rec/2411

Chicago Manual of Style (16th Edition):

Veerappan, Chendhore Sai. “Epigenetic plasticity of cultured female human embryonic stem cells and regulation of gene expression and chromatin by PR-SET7 mediated H4K20me1.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112300/rec/2411.

MLA Handbook (7th Edition):

Veerappan, Chendhore Sai. “Epigenetic plasticity of cultured female human embryonic stem cells and regulation of gene expression and chromatin by PR-SET7 mediated H4K20me1.” 2012. Web. 22 Jan 2020.

Vancouver:

Veerappan CS. Epigenetic plasticity of cultured female human embryonic stem cells and regulation of gene expression and chromatin by PR-SET7 mediated H4K20me1. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112300/rec/2411.

Council of Science Editors:

Veerappan CS. Epigenetic plasticity of cultured female human embryonic stem cells and regulation of gene expression and chromatin by PR-SET7 mediated H4K20me1. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112300/rec/2411


University of Southern California

19. Anderson, Lindsey Jayne. Influence of endogenous and exogenous estrogen on skeletal muscle damage and systemic inflammation after electrically stimulated contraction in young women.

Degree: PhD, Biokinesiology and Physical Therapy, 2015, University of Southern California

 Exercise is a key regulator of skeletal muscle health as repeated exposure to acute bouts of exercise constitutes muscular adaptation to exercise training. The influence… (more)

Subjects/Keywords: exercise; skeletal muscle; muscle damage; estrogen; estradiol; oral contraceptives; young women; ethinyl estradiol

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APA (6th Edition):

Anderson, L. J. (2015). Influence of endogenous and exogenous estrogen on skeletal muscle damage and systemic inflammation after electrically stimulated contraction in young women. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/584653/rec/3477

Chicago Manual of Style (16th Edition):

Anderson, Lindsey Jayne. “Influence of endogenous and exogenous estrogen on skeletal muscle damage and systemic inflammation after electrically stimulated contraction in young women.” 2015. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/584653/rec/3477.

MLA Handbook (7th Edition):

Anderson, Lindsey Jayne. “Influence of endogenous and exogenous estrogen on skeletal muscle damage and systemic inflammation after electrically stimulated contraction in young women.” 2015. Web. 22 Jan 2020.

Vancouver:

Anderson LJ. Influence of endogenous and exogenous estrogen on skeletal muscle damage and systemic inflammation after electrically stimulated contraction in young women. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/584653/rec/3477.

Council of Science Editors:

Anderson LJ. Influence of endogenous and exogenous estrogen on skeletal muscle damage and systemic inflammation after electrically stimulated contraction in young women. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/584653/rec/3477


University of Southern California

20. 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 January 22, 2020. 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. 22 Jan 2020.

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 2020 Jan 22]. 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

21. Wolff, Erika Michele. Epigenetic mechanisms driving bladder cancer.

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

 Successes in the clinic have opened up the era of epigenetic therapy in which the goal is to reactivate genes silenced inappropriately during carcinogenesis. The… (more)

Subjects/Keywords: epigenetics; methylation; bladder cancer

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APA (6th Edition):

Wolff, E. M. (2009). Epigenetic mechanisms driving bladder cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/181217/rec/2410

Chicago Manual of Style (16th Edition):

Wolff, Erika Michele. “Epigenetic mechanisms driving bladder cancer.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/181217/rec/2410.

MLA Handbook (7th Edition):

Wolff, Erika Michele. “Epigenetic mechanisms driving bladder cancer.” 2009. Web. 22 Jan 2020.

Vancouver:

Wolff EM. Epigenetic mechanisms driving bladder cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/181217/rec/2410.

Council of Science Editors:

Wolff EM. Epigenetic mechanisms driving bladder cancer. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/181217/rec/2410


University of Southern California

22. Cortez, Connie C. Epigenetic regulation of non CPG island gene promoters.

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

 DNA methylation and post-translational modifications of histones can specify transcriptional competency in both normal and cancer cells. However these epigenetic processes have largely been studied… (more)

Subjects/Keywords: epigenetics; DNA methylation; LAMB3; RUNX3

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APA (6th Edition):

Cortez, C. C. (2008). Epigenetic regulation of non CPG island gene promoters. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/132193/rec/2412

Chicago Manual of Style (16th Edition):

Cortez, Connie C. “Epigenetic regulation of non CPG island gene promoters.” 2008. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/132193/rec/2412.

MLA Handbook (7th Edition):

Cortez, Connie C. “Epigenetic regulation of non CPG island gene promoters.” 2008. Web. 22 Jan 2020.

Vancouver:

Cortez CC. Epigenetic regulation of non CPG island gene promoters. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/132193/rec/2412.

Council of Science Editors:

Cortez CC. Epigenetic regulation of non CPG island gene promoters. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/132193/rec/2412


University of Southern California

23. Pregizer, Steven. Runx2 interactions with the osteoblast genome.

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

 Runx2 is a master transcription factor in osteoblasts, yet its mechanism is poorly understood. In particular, there is a paucity of information about its target… (more)

Subjects/Keywords: Runx2; osteoblast differentiation; transcriptional regulation; location analysis

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APA (6th Edition):

Pregizer, S. (2008). Runx2 interactions with the osteoblast genome. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5661

Chicago Manual of Style (16th Edition):

Pregizer, Steven. “Runx2 interactions with the osteoblast genome.” 2008. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5661.

MLA Handbook (7th Edition):

Pregizer, Steven. “Runx2 interactions with the osteoblast genome.” 2008. Web. 22 Jan 2020.

Vancouver:

Pregizer S. Runx2 interactions with the osteoblast genome. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5661.

Council of Science Editors:

Pregizer S. Runx2 interactions with the osteoblast genome. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5661


University of Southern California

24. Heo, Kyu. Investigation of two distinct chromatin events: H3 tail-mediated factor recruitment and H2A.X exchange.

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

 Posttranslational modifications of histones, ATP-dependent chromatin remodeling, and incorporation of histone variants are three major events to regulate DNA dependent processes in chromatin context.; Histones… (more)

Subjects/Keywords: histone chromatin

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APA (6th Edition):

Heo, K. (2007). Investigation of two distinct chromatin events: H3 tail-mediated factor recruitment and H2A.X exchange. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484083/rec/3648

Chicago Manual of Style (16th Edition):

Heo, Kyu. “Investigation of two distinct chromatin events: H3 tail-mediated factor recruitment and H2A.X exchange.” 2007. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484083/rec/3648.

MLA Handbook (7th Edition):

Heo, Kyu. “Investigation of two distinct chromatin events: H3 tail-mediated factor recruitment and H2A.X exchange.” 2007. Web. 22 Jan 2020.

Vancouver:

Heo K. Investigation of two distinct chromatin events: H3 tail-mediated factor recruitment and H2A.X exchange. [Internet] [Doctoral dissertation]. University of Southern California; 2007. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484083/rec/3648.

Council of Science Editors:

Heo K. Investigation of two distinct chromatin events: H3 tail-mediated factor recruitment and H2A.X exchange. [Doctoral Dissertation]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484083/rec/3648


University of Southern California

25. 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/1933

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 January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/117489/rec/1933.

MLA Handbook (7th Edition):

Galler, Janice Soratorio. “Development of DNA methylation biomarkers as an early detection tool for human lung adenocarcinoma.” 2008. Web. 22 Jan 2020.

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 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/117489/rec/1933.

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/1933


University of Southern California

26. 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/1932

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 January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/142191/rec/1932.

MLA Handbook (7th Edition):

Anglim, Paul P. “Development of DNA methylation based biomarkers for the early detection of squamous cell lung cancer.” 2008. Web. 22 Jan 2020.

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 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/142191/rec/1932.

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/1932


University of Southern California

27. Viggiani, Christopher John. New tools for whole-genome analysis of DNA replication timing and fork elongation in saccharomyces cerevisiae.

Degree: PhD, Biology, 2007, University of Southern California

 The faithful duplication of the genome during S phase is critical to a eukaryotic cell's healthy proliferation. Since errors in DNA replication can lead to… (more)

Subjects/Keywords: DNA replication; BrdU; Sin3-Rpd3; chromatin structure; replication forks; replication origin initiation

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APA (6th Edition):

Viggiani, C. J. (2007). New tools for whole-genome analysis of DNA replication timing and fork elongation in saccharomyces cerevisiae. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/515107/rec/4406

Chicago Manual of Style (16th Edition):

Viggiani, Christopher John. “New tools for whole-genome analysis of DNA replication timing and fork elongation in saccharomyces cerevisiae.” 2007. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/515107/rec/4406.

MLA Handbook (7th Edition):

Viggiani, Christopher John. “New tools for whole-genome analysis of DNA replication timing and fork elongation in saccharomyces cerevisiae.” 2007. Web. 22 Jan 2020.

Vancouver:

Viggiani CJ. New tools for whole-genome analysis of DNA replication timing and fork elongation in saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Southern California; 2007. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/515107/rec/4406.

Council of Science Editors:

Viggiani CJ. New tools for whole-genome analysis of DNA replication timing and fork elongation in saccharomyces cerevisiae. [Doctoral Dissertation]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/515107/rec/4406


University of Southern California

28. Szyjka, Shawn Joseph. The intra-S phase checkpoint and its effect on replication fork dynamics in saccharomyces cerevisiae.

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

 Duplication of a cell's genetic material is of paramount importance. This task must be completed accurately, efficiently and occur once and only once within any… (more)

Subjects/Keywords: DNA replication; DNA damage; replication fork; DNA repair; cell cycle checkpoint; phosphatase; Rad53; Mrc1; BrdU; microarray; Claspin; replication fork progression; Rrm3; Pph3; 2-D gel electro

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APA (6th Edition):

Szyjka, S. J. (2008). The intra-S phase checkpoint and its effect on replication fork dynamics in saccharomyces cerevisiae. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/119913/rec/6914

Chicago Manual of Style (16th Edition):

Szyjka, Shawn Joseph. “The intra-S phase checkpoint and its effect on replication fork dynamics in saccharomyces cerevisiae.” 2008. Doctoral Dissertation, University of Southern California. Accessed January 22, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/119913/rec/6914.

MLA Handbook (7th Edition):

Szyjka, Shawn Joseph. “The intra-S phase checkpoint and its effect on replication fork dynamics in saccharomyces cerevisiae.” 2008. Web. 22 Jan 2020.

Vancouver:

Szyjka SJ. The intra-S phase checkpoint and its effect on replication fork dynamics in saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Jan 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/119913/rec/6914.

Council of Science Editors:

Szyjka SJ. The intra-S phase checkpoint and its effect on replication fork dynamics in saccharomyces cerevisiae. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/119913/rec/6914

.