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You searched for +publisher:"University of Southern California" +contributor:("Chen, Lin"). Showing records 1 – 19 of 19 total matches.

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University of Southern California

1. Tsai, Sophia Jan. Structure and regulation of lymphoid tyrosine phosphatase (LYP) in autoimmune response.

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

 Protein tyrosine kinases and protein tyrosine phosphatases maintain a delicate balance via signaling in the human body. LYP is a cytosolic classical tyrosine phosphatase, known… (more)

Subjects/Keywords: autoimmunity; LYP; PTPN22; regulation; T-cell signalling; X-ray crystallography

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APA (6th Edition):

Tsai, S. J. (2012). Structure and regulation of lymphoid tyrosine phosphatase (LYP) in autoimmune response. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/337794/rec/6125

Chicago Manual of Style (16th Edition):

Tsai, Sophia Jan. “Structure and regulation of lymphoid tyrosine phosphatase (LYP) in autoimmune response.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/337794/rec/6125.

MLA Handbook (7th Edition):

Tsai, Sophia Jan. “Structure and regulation of lymphoid tyrosine phosphatase (LYP) in autoimmune response.” 2012. Web. 29 Jan 2020.

Vancouver:

Tsai SJ. Structure and regulation of lymphoid tyrosine phosphatase (LYP) in autoimmune response. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/337794/rec/6125.

Council of Science Editors:

Tsai SJ. Structure and regulation of lymphoid tyrosine phosphatase (LYP) in autoimmune response. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/337794/rec/6125


University of Southern California

2. Hu, Biliang. Lentiviral vaccine engineering towards enhanced safety and efficiency.

Degree: PhD, Chemical Engineering, 2013, University of Southern California

 Extensive understanding of the lentivirus biology has evolved the design of lentivector (LV) for therapeutic gene delivery, and transformed lentivector to one of the most… (more)

Subjects/Keywords: cancer immunotherapy; CD8 T cell; dendritic cell; lentivector; transgene integration; tumor microenvironment

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APA (6th Edition):

Hu, B. (2013). Lentiviral vaccine engineering towards enhanced safety and efficiency. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795

Chicago Manual of Style (16th Edition):

Hu, Biliang. “Lentiviral vaccine engineering towards enhanced safety and efficiency.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795.

MLA Handbook (7th Edition):

Hu, Biliang. “Lentiviral vaccine engineering towards enhanced safety and efficiency.” 2013. Web. 29 Jan 2020.

Vancouver:

Hu B. Lentiviral vaccine engineering towards enhanced safety and efficiency. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795.

Council of Science Editors:

Hu B. Lentiviral vaccine engineering towards enhanced safety and efficiency. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795


University of Southern California

3. Li, Yang. The polydispersity of human FOXP3 fragment with zinc finger, leucine zipper and forkhead domain.

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

 Forkhead Box Protein P3 (FOXP3) is essential for the development and maintenance of regulatory T cells (Treg) via regulating the expression of genes involved in… (more)

Subjects/Keywords: forkhead domain; polydispersity; zinc finger; structure

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APA (6th Edition):

Li, Y. (2010). The polydispersity of human FOXP3 fragment with zinc finger, leucine zipper and forkhead domain. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384355/rec/7099

Chicago Manual of Style (16th Edition):

Li, Yang. “The polydispersity of human FOXP3 fragment with zinc finger, leucine zipper and forkhead domain.” 2010. Masters Thesis, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384355/rec/7099.

MLA Handbook (7th Edition):

Li, Yang. “The polydispersity of human FOXP3 fragment with zinc finger, leucine zipper and forkhead domain.” 2010. Web. 29 Jan 2020.

Vancouver:

Li Y. The polydispersity of human FOXP3 fragment with zinc finger, leucine zipper and forkhead domain. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384355/rec/7099.

Council of Science Editors:

Li Y. The polydispersity of human FOXP3 fragment with zinc finger, leucine zipper and forkhead domain. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/384355/rec/7099


University of Southern California

4. Jayathilaka, Nimanthi. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.

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

 Enzymes that modify epigenetic status provide attractive targets for therapy in various diseases including cardiac hypertrophy, cancer, neurodegenerative diseases, and immune dysfunction. The therapeutic development… (more)

Subjects/Keywords: histone deacetylases (HDAC); HDAC inhibitors; myocyte enhancer factor 2 (MEF2); transcription regulation

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APA (6th Edition):

Jayathilaka, N. (2012). Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496

Chicago Manual of Style (16th Edition):

Jayathilaka, Nimanthi. “Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496.

MLA Handbook (7th Edition):

Jayathilaka, Nimanthi. “Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.” 2012. Web. 29 Jan 2020.

Vancouver:

Jayathilaka N. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496.

Council of Science Editors:

Jayathilaka N. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496


University of Southern California

5. Zhou, Bo. Structural and biochemical studies of large T antigen: the SV40 replicative helicase.

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

 Simian Virus 40 (SV40) replication has long been regarded as a useful model system in circumventing the complexity of studying the eukaryotic DNA replication process.… (more)

Subjects/Keywords: large T antigen; helicase; DNA polymerase; Primase; DNA replication; crystallography

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APA (6th Edition):

Zhou, B. (2012). Structural and biochemical studies of large T antigen: the SV40 replicative helicase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106

Chicago Manual of Style (16th Edition):

Zhou, Bo. “Structural and biochemical studies of large T antigen: the SV40 replicative helicase.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106.

MLA Handbook (7th Edition):

Zhou, Bo. “Structural and biochemical studies of large T antigen: the SV40 replicative helicase.” 2012. Web. 29 Jan 2020.

Vancouver:

Zhou B. Structural and biochemical studies of large T antigen: the SV40 replicative helicase. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106.

Council of Science Editors:

Zhou B. Structural and biochemical studies of large T antigen: the SV40 replicative helicase. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106


University of Southern California

6. Xu, Meng. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.

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

 The hetero-hexamer of the eukaryotic minichromosome maintenance (MCM) proteins plays an essential role in replication of genomic DNA. The ring-shaped Mcm2-7 hexamers comprising one of… (more)

Subjects/Keywords: helicase; cell cycle proteins; DNA-binding proteins; recombinant proteins; protein binding; protein oligomerization; schizosaccharomyces pombe; Escherichiai coli; simian virus 40

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APA (6th Edition):

Xu, M. (2012). Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106

Chicago Manual of Style (16th Edition):

Xu, Meng. “Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106.

MLA Handbook (7th Edition):

Xu, Meng. “Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.” 2012. Web. 29 Jan 2020.

Vancouver:

Xu M. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106.

Council of Science Editors:

Xu M. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106


University of Southern California

7. Zaro, Balyn Wood. Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping.

Degree: PhD, Chemistry, 2014, University of Southern California

 Post-translational modifications (PTMs) are ancillary decorations that are transferred onto fully-synthesized proteins. These modifications have been shown to significantly alter the fate and function of… (more)

Subjects/Keywords: O-GlcNAc; carbohydrates; chemical reporters; click chemistry; acetylation; post-translational modifications

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APA (6th Edition):

Zaro, B. W. (2014). Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4604

Chicago Manual of Style (16th Edition):

Zaro, Balyn Wood. “Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4604.

MLA Handbook (7th Edition):

Zaro, Balyn Wood. “Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping.” 2014. Web. 29 Jan 2020.

Vancouver:

Zaro BW. Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4604.

Council of Science Editors:

Zaro BW. Optimization of chemical reporters of O-GlcNAc for improved specificity and metabolic mapping. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/476825/rec/4604


University of Southern California

8. Grant, Gian Paola Gacho. Motions and conformations of nucleic acids studied using site-directed spin labeling.

Degree: PhD, Chemistry, 2009, University of Southern California

 Deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) play crucial roles in life. They carry and transmit genetic information, regulate and maintain gene expression, and in… (more)

Subjects/Keywords: site-directed spin labeling; DNA; RNA; structure; dynamics; EPR

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APA (6th Edition):

Grant, G. P. G. (2009). Motions and conformations of nucleic acids studied using site-directed spin labeling. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225

Chicago Manual of Style (16th Edition):

Grant, Gian Paola Gacho. “Motions and conformations of nucleic acids studied using site-directed spin labeling.” 2009. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225.

MLA Handbook (7th Edition):

Grant, Gian Paola Gacho. “Motions and conformations of nucleic acids studied using site-directed spin labeling.” 2009. Web. 29 Jan 2020.

Vancouver:

Grant GPG. Motions and conformations of nucleic acids studied using site-directed spin labeling. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225.

Council of Science Editors:

Grant GPG. Motions and conformations of nucleic acids studied using site-directed spin labeling. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225


University of Southern California

9. Philips, Michael Albert. Using novel small molecule modulators as a tool to elucidate the role of the Myocyte Enhancer Factor 2 (MEF2) family of transcription factors in leukemia.

Degree: PhD, Molecular Biology, 2013, University of Southern California

 The Myocyte Enhancer Factor 2 (MEF2) family of transcription factors are DNA-bound proteins that regulate gene expression via their interaction with co-regulatory proteins. This interaction… (more)

Subjects/Keywords: MEF2; HDAC; HDACi; leukemia; NKL-30; BML-210; 2-aminobenzamide; Imatinib Mesylate; Gleevec; Myocyte Enhancer Factor 2; histone deacetylase; histone deacetylase inhibitor; acute lymphoblastic leukemia; B cells; Nalm6; GM12878; epigenetics; crystallography; mRNA-seq

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APA (6th Edition):

Philips, M. A. (2013). Using novel small molecule modulators as a tool to elucidate the role of the Myocyte Enhancer Factor 2 (MEF2) family of transcription factors in leukemia. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323542/rec/7761

Chicago Manual of Style (16th Edition):

Philips, Michael Albert. “Using novel small molecule modulators as a tool to elucidate the role of the Myocyte Enhancer Factor 2 (MEF2) family of transcription factors in leukemia.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323542/rec/7761.

MLA Handbook (7th Edition):

Philips, Michael Albert. “Using novel small molecule modulators as a tool to elucidate the role of the Myocyte Enhancer Factor 2 (MEF2) family of transcription factors in leukemia.” 2013. Web. 29 Jan 2020.

Vancouver:

Philips MA. Using novel small molecule modulators as a tool to elucidate the role of the Myocyte Enhancer Factor 2 (MEF2) family of transcription factors in leukemia. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323542/rec/7761.

Council of Science Editors:

Philips MA. Using novel small molecule modulators as a tool to elucidate the role of the Myocyte Enhancer Factor 2 (MEF2) family of transcription factors in leukemia. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323542/rec/7761


University of Southern California

10. Noridomi, Kaori. Structural studies of nicotinic acetylcholine receptors and their regulatory complexes.

Degree: PhD, Chemistry, 2017, University of Southern California

 Nicotinic acetylcholine receptors (nAChRs) play a key role in neuronal communication by sending electric signals upon binding of neurotransmitters, acetylcholines. nAChRs relate closely to various… (more)

Subjects/Keywords: nicotinic acetylcholine receptors; crystal structure; crystallography; myasthenia gravis

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APA (6th Edition):

Noridomi, K. (2017). Structural studies of nicotinic acetylcholine receptors and their regulatory complexes. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117

Chicago Manual of Style (16th Edition):

Noridomi, Kaori. “Structural studies of nicotinic acetylcholine receptors and their regulatory complexes.” 2017. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117.

MLA Handbook (7th Edition):

Noridomi, Kaori. “Structural studies of nicotinic acetylcholine receptors and their regulatory complexes.” 2017. Web. 29 Jan 2020.

Vancouver:

Noridomi K. Structural studies of nicotinic acetylcholine receptors and their regulatory complexes. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117.

Council of Science Editors:

Noridomi K. Structural studies of nicotinic acetylcholine receptors and their regulatory complexes. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117


University of Southern California

11. Ostrow, Andrew Zachary. Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae.

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

 Forkhead box (FOX) transcription factors regulate a wide variety of cellular functions in higher eukaryotes, including cell cycle control and developmental regulation. In Saccharomyces cerevisiae,… (more)

Subjects/Keywords: replication timing; chromatin; Fkh1; Fkh2; Forkhead; transcription factors; dimer; dimers; dimerization; replication foci; genome architecture; genome structure; chromatin organization; replication origins

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APA (6th Edition):

Ostrow, A. Z. (2015). Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870

Chicago Manual of Style (16th Edition):

Ostrow, Andrew Zachary. “Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae.” 2015. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870.

MLA Handbook (7th Edition):

Ostrow, Andrew Zachary. “Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae.” 2015. Web. 29 Jan 2020.

Vancouver:

Ostrow AZ. Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870.

Council of Science Editors:

Ostrow AZ. Forkhead transcription factors regulate replication origin firing through dimerization and cell cycle-dependent chromatin binding in S. cerevisiae. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/520750/rec/2870


University of Southern California

12. Al-Bassam, Sarmad. A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons.

Degree: PhD, Molecular Biology, 2013, University of Southern California

 In neurons transmembrane proteins are targeted to dendrites in vesicles that traffic solely within the somatodendritic compartment. How these vesicles are retained within the somatodendritic… (more)

Subjects/Keywords: polarized trafficking; dissociated neurons; vesicle transport; axon tnitial segment; FKBP; conditional aggregation domain; shield-1; pulse-chase

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APA (6th Edition):

Al-Bassam, S. (2013). A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287

Chicago Manual of Style (16th Edition):

Al-Bassam, Sarmad. “A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287.

MLA Handbook (7th Edition):

Al-Bassam, Sarmad. “A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons.” 2013. Web. 29 Jan 2020.

Vancouver:

Al-Bassam S. A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287.

Council of Science Editors:

Al-Bassam S. A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287


University of Southern California

13. Lewis, Tommy L., Jr. Myosin-dependent targeting of transmembrane proteins in neurons.

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

 In neurons polarized trafficking of vesicle-bound membrane proteins gives rise to the distinct molecular composition and functional properties of axons and dendrites. Despite their central… (more)

Subjects/Keywords: myosin; neuron; dendritic targeting; cell biology; targeting; actin; Channelrhodopsin 2; vesicle filter

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APA (6th Edition):

Lewis, Tommy L., J. (2011). Myosin-dependent targeting of transmembrane proteins in neurons. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/335986/rec/4302

Chicago Manual of Style (16th Edition):

Lewis, Tommy L., Jr. “Myosin-dependent targeting of transmembrane proteins in neurons.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/335986/rec/4302.

MLA Handbook (7th Edition):

Lewis, Tommy L., Jr. “Myosin-dependent targeting of transmembrane proteins in neurons.” 2011. Web. 29 Jan 2020.

Vancouver:

Lewis, Tommy L. J. Myosin-dependent targeting of transmembrane proteins in neurons. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/335986/rec/4302.

Council of Science Editors:

Lewis, Tommy L. J. Myosin-dependent targeting of transmembrane proteins in neurons. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/335986/rec/4302


University of Southern California

14. Kalhor, Reza. Exploring three-dimensional organization of the genome by mapping chromatin contacts and population modeling.

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

 The genetic information in most organisms is stored in a double-helical fiber molecule known as DNA. The total DNA fiber inside every single human nucleus,… (more)

Subjects/Keywords: chromosome conformation capture; genome architecture; chromatin structure; TCC; Tethered Conformation Capture; Hi-C; Population-based modeling; population modeling; chromosome structure

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APA (6th Edition):

Kalhor, R. (2012). Exploring three-dimensional organization of the genome by mapping chromatin contacts and population modeling. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44451/rec/2678

Chicago Manual of Style (16th Edition):

Kalhor, Reza. “Exploring three-dimensional organization of the genome by mapping chromatin contacts and population modeling.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44451/rec/2678.

MLA Handbook (7th Edition):

Kalhor, Reza. “Exploring three-dimensional organization of the genome by mapping chromatin contacts and population modeling.” 2012. Web. 29 Jan 2020.

Vancouver:

Kalhor R. Exploring three-dimensional organization of the genome by mapping chromatin contacts and population modeling. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44451/rec/2678.

Council of Science Editors:

Kalhor R. Exploring three-dimensional organization of the genome by mapping chromatin contacts and population modeling. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44451/rec/2678


University of Southern California

15. Watanabe, Go. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.

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

 Nonhomologous DNA end joining (NHEJ) is the major repair mechanism for double‐strand DNA breaks. One of the key components in human NHEJ is DNA‐dependent protein… (more)

Subjects/Keywords: DNA repair; NHEJ; DNA-PKcs; X-ray crystallography

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

APA (6th Edition):

Watanabe, G. (2017). X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971

Chicago Manual of Style (16th Edition):

Watanabe, Go. “X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.” 2017. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971.

MLA Handbook (7th Edition):

Watanabe, Go. “X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals.” 2017. Web. 29 Jan 2020.

Vancouver:

Watanabe G. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971.

Council of Science Editors:

Watanabe G. X-ray structural studies on DNA-dependent protein kinase catalytic subunit:DNA co-crystals. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/583888/rec/7971


University of Southern California

16. Holden, Lauren Georgianna. A structure based study of the HIV restriction factor APOBEC3G.

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

 The Apolipoprotein B editing enzyme catalytic polypeptide-like (APOBEC) family of 11 proteins deaminate cytidines on either single-stranded DNA (ssDNA) or RNA substrates, introducing C to… (more)

Subjects/Keywords: cytidine deaminase; X-ray crystallography; anti-HIV

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

APA (6th Edition):

Holden, L. G. (2011). A structure based study of the HIV restriction factor APOBEC3G. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376

Chicago Manual of Style (16th Edition):

Holden, Lauren Georgianna. “A structure based study of the HIV restriction factor APOBEC3G.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376.

MLA Handbook (7th Edition):

Holden, Lauren Georgianna. “A structure based study of the HIV restriction factor APOBEC3G.” 2011. Web. 29 Jan 2020.

Vancouver:

Holden LG. A structure based study of the HIV restriction factor APOBEC3G. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376.

Council of Science Editors:

Holden LG. A structure based study of the HIV restriction factor APOBEC3G. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/416237/rec/376


University of Southern California

17. Peace, Jared Michael. Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program.

Degree: PhD, Molecular Biology, 2014, University of Southern California

 Eukaryotic cells initiate DNA replication from hundreds to thousands of origins genome wide. The coordinated firing of these origins across a range of times throughout… (more)

Subjects/Keywords: Forkhead; Fkh1; Fkh2; Cdc45; Rif1; Rap1; Pfa4; Mec1; Cdc7; Dbf4; Dbf4 Dependent Kinase (DDK); Orc1; replication origin timing; replication fork rate; chromatin; centromere; telomere; epigenetics; transcription; nuclear architecture; S. cerevisiae

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

APA (6th Edition):

Peace, J. M. (2014). Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869

Chicago Manual of Style (16th Edition):

Peace, Jared Michael. “Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869.

MLA Handbook (7th Edition):

Peace, Jared Michael. “Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program.” 2014. Web. 29 Jan 2020.

Vancouver:

Peace JM. Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869.

Council of Science Editors:

Peace JM. Forkhead transcription factors control genome wide dynamics of the S. cerevisiae replication timing program. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/514469/rec/2869


University of Southern California

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

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 29, 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. 29 Jan 2020.

Vancouver:

Li P. The centromere: replication, recombination, reassembly. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Jan 29]. 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

19. Prochnow, Courtney. The crystal structure of APOBEC-2 and implications for APOBEC enzymes.

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

 APOBEC-2 (Apo2) belongs to the Apolioprotein B (APOB) mRNA-editing enzyme catalytic polypeptide (APOBEC) family of cytidine deaminases that modify genes by deaminating cytosines in mRNA… (more)

Subjects/Keywords: APOBEC; cytidine deaminase; HIV; cytidine deamination; activation induced cytidine deaminase; AID; APOBEC-2

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

APA (6th Edition):

Prochnow, C. (2008). The crystal structure of APOBEC-2 and implications for APOBEC enzymes. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531

Chicago Manual of Style (16th Edition):

Prochnow, Courtney. “The crystal structure of APOBEC-2 and implications for APOBEC enzymes.” 2008. Doctoral Dissertation, University of Southern California. Accessed January 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531.

MLA Handbook (7th Edition):

Prochnow, Courtney. “The crystal structure of APOBEC-2 and implications for APOBEC enzymes.” 2008. Web. 29 Jan 2020.

Vancouver:

Prochnow C. The crystal structure of APOBEC-2 and implications for APOBEC enzymes. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Jan 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531.

Council of Science Editors:

Prochnow C. The crystal structure of APOBEC-2 and implications for APOBEC enzymes. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/39667/rec/6531

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