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You searched for +publisher:"University of Illinois – Urbana-Champaign" +contributor:("Katzenellenbogen, Benita S"). Showing records 1 – 23 of 23 total matches.

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University of Illinois – Urbana-Champaign

1. Barnett, Daniel H. Identification and characterization of estrogen receptor-regulated gene expression programs.

Degree: PhD, 4094, 2010, University of Illinois – Urbana-Champaign

 The physiological effects of natural and synthetic estrogens are mediated by estrogen receptor alpha (ER alpha), and estrogen receptor beta (ER beta). Within the nucleus… (more)

Subjects/Keywords: Estrogen; Estradiol; Estrogen Receptor; Gene Regulation, Tamoxifen; Raloxifene; SERM; Transcription; Enhancer; Carbonic Anhydrase; Chromatin

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APA (6th Edition):

Barnett, D. H. (2010). Identification and characterization of estrogen receptor-regulated gene expression programs. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15500

Chicago Manual of Style (16th Edition):

Barnett, Daniel H. “Identification and characterization of estrogen receptor-regulated gene expression programs.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/15500.

MLA Handbook (7th Edition):

Barnett, Daniel H. “Identification and characterization of estrogen receptor-regulated gene expression programs.” 2010. Web. 16 Sep 2019.

Vancouver:

Barnett DH. Identification and characterization of estrogen receptor-regulated gene expression programs. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/15500.

Council of Science Editors:

Barnett DH. Identification and characterization of estrogen receptor-regulated gene expression programs. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15500


University of Illinois – Urbana-Champaign

2. Bhatt, Shweta. Cross-modulatory Actions of Cell Cycle Machinery on Estrogen Receptor-alpha Level and Transcriptional Activity in Breast Cancer Cells.

Degree: PhD, 0318, 2010, University of Illinois – Urbana-Champaign

 Breast cancer is one of the most highly diagnosed cancers in women and the second largest cause of death of women in United States. The… (more)

Subjects/Keywords: Estrogen Receptor signaling; Breast Cancer; Skp2 mediated Ubiquitination; p38MAPK signaling; Cell cycle regulation in Breast cancer cells.

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APA (6th Edition):

Bhatt, S. (2010). Cross-modulatory Actions of Cell Cycle Machinery on Estrogen Receptor-alpha Level and Transcriptional Activity in Breast Cancer Cells. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/17032

Chicago Manual of Style (16th Edition):

Bhatt, Shweta. “Cross-modulatory Actions of Cell Cycle Machinery on Estrogen Receptor-alpha Level and Transcriptional Activity in Breast Cancer Cells.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/17032.

MLA Handbook (7th Edition):

Bhatt, Shweta. “Cross-modulatory Actions of Cell Cycle Machinery on Estrogen Receptor-alpha Level and Transcriptional Activity in Breast Cancer Cells.” 2010. Web. 16 Sep 2019.

Vancouver:

Bhatt S. Cross-modulatory Actions of Cell Cycle Machinery on Estrogen Receptor-alpha Level and Transcriptional Activity in Breast Cancer Cells. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/17032.

Council of Science Editors:

Bhatt S. Cross-modulatory Actions of Cell Cycle Machinery on Estrogen Receptor-alpha Level and Transcriptional Activity in Breast Cancer Cells. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/17032


University of Illinois – Urbana-Champaign

3. Funk, Cory C. Estradiol regulation of leucine-rich repeat immunoglobulin-like domains protein 1 (LRIG 1) and roles of estrogen receptor in translational regulation in breast cancer cells.

Degree: PhD, 4094, 2011, University of Illinois – Urbana-Champaign

 Among the first diagnostic tests performed upon finding a tumor in the breast is the determination of the expression of three proteins: the Estrogen Receptor… (more)

Subjects/Keywords: LRIG1; eIF3f; breast cancer; estrogen receptor; translation; gene regulation; transcription; chromatin

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APA (6th Edition):

Funk, C. C. (2011). Estradiol regulation of leucine-rich repeat immunoglobulin-like domains protein 1 (LRIG 1) and roles of estrogen receptor in translational regulation in breast cancer cells. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18651

Chicago Manual of Style (16th Edition):

Funk, Cory C. “Estradiol regulation of leucine-rich repeat immunoglobulin-like domains protein 1 (LRIG 1) and roles of estrogen receptor in translational regulation in breast cancer cells.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/18651.

MLA Handbook (7th Edition):

Funk, Cory C. “Estradiol regulation of leucine-rich repeat immunoglobulin-like domains protein 1 (LRIG 1) and roles of estrogen receptor in translational regulation in breast cancer cells.” 2011. Web. 16 Sep 2019.

Vancouver:

Funk CC. Estradiol regulation of leucine-rich repeat immunoglobulin-like domains protein 1 (LRIG 1) and roles of estrogen receptor in translational regulation in breast cancer cells. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/18651.

Council of Science Editors:

Funk CC. Estradiol regulation of leucine-rich repeat immunoglobulin-like domains protein 1 (LRIG 1) and roles of estrogen receptor in translational regulation in breast cancer cells. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18651


University of Illinois – Urbana-Champaign

4. Kim, Kyuri. Regulation of estrogen receptor-alpha mediated gene expression and endocrine resistance through estrogen receptor-alpha phosphorylation and micro-RNA in breast cancer.

Degree: PhD, 0325, 2011, University of Illinois – Urbana-Champaign

 Estrogens are associated with the development and progression of breast cancer in addition to their role in normal reproductive physiology, and estrogen receptors (ER) mediate… (more)

Subjects/Keywords: Estrogen Receptor; Endocrine Resistance; Breast Cancer; microRNA; Phosphorylation

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APA (6th Edition):

Kim, K. (2011). Regulation of estrogen receptor-alpha mediated gene expression and endocrine resistance through estrogen receptor-alpha phosphorylation and micro-RNA in breast cancer. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24407

Chicago Manual of Style (16th Edition):

Kim, Kyuri. “Regulation of estrogen receptor-alpha mediated gene expression and endocrine resistance through estrogen receptor-alpha phosphorylation and micro-RNA in breast cancer.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/24407.

MLA Handbook (7th Edition):

Kim, Kyuri. “Regulation of estrogen receptor-alpha mediated gene expression and endocrine resistance through estrogen receptor-alpha phosphorylation and micro-RNA in breast cancer.” 2011. Web. 16 Sep 2019.

Vancouver:

Kim K. Regulation of estrogen receptor-alpha mediated gene expression and endocrine resistance through estrogen receptor-alpha phosphorylation and micro-RNA in breast cancer. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/24407.

Council of Science Editors:

Kim K. Regulation of estrogen receptor-alpha mediated gene expression and endocrine resistance through estrogen receptor-alpha phosphorylation and micro-RNA in breast cancer. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24407


University of Illinois – Urbana-Champaign

5. Park, Sung Hee. Repressor of Estrogen Receptor Activity (REA) is a gene dose-dependent coregulator protein affecting estrogen signaling and cell survival.

Degree: PhD, 0325, 2011, University of Illinois – Urbana-Champaign

 Repressor of Estrogen Receptor Activity (REA) is an evolutionarily conserved protein with established roles in multiple, essential cellular processes including transcription, mitochondrial biogenesis and replicative… (more)

Subjects/Keywords: estrogen; transcription; coregualator; uterus; mammary gland

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APA (6th Edition):

Park, S. H. (2011). Repressor of Estrogen Receptor Activity (REA) is a gene dose-dependent coregulator protein affecting estrogen signaling and cell survival. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24368

Chicago Manual of Style (16th Edition):

Park, Sung Hee. “Repressor of Estrogen Receptor Activity (REA) is a gene dose-dependent coregulator protein affecting estrogen signaling and cell survival.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/24368.

MLA Handbook (7th Edition):

Park, Sung Hee. “Repressor of Estrogen Receptor Activity (REA) is a gene dose-dependent coregulator protein affecting estrogen signaling and cell survival.” 2011. Web. 16 Sep 2019.

Vancouver:

Park SH. Repressor of Estrogen Receptor Activity (REA) is a gene dose-dependent coregulator protein affecting estrogen signaling and cell survival. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/24368.

Council of Science Editors:

Park SH. Repressor of Estrogen Receptor Activity (REA) is a gene dose-dependent coregulator protein affecting estrogen signaling and cell survival. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24368


University of Illinois – Urbana-Champaign

6. Charn, Tze Howe. An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells.

Degree: PhD, 0408, 2011, University of Illinois – Urbana-Champaign

 The nuclear hormone receptors, ER?? and ER??, are known to regulate the transcriptional response programs of their target cells, including breast cancer cells. However, their… (more)

Subjects/Keywords: Estrogen receptors; MCF-7; nuclear receptor coactivator 3 (SRC3); RIP140

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APA (6th Edition):

Charn, T. H. (2011). An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18589

Chicago Manual of Style (16th Edition):

Charn, Tze Howe. “An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/18589.

MLA Handbook (7th Edition):

Charn, Tze Howe. “An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells.” 2011. Web. 16 Sep 2019.

Vancouver:

Charn TH. An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/18589.

Council of Science Editors:

Charn TH. An integrated network of estrogen receptors alpha and beta, and coregulators, for deciphering estrogen signaling in breast cancer cells. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18589


University of Illinois – Urbana-Champaign

7. Ge, Yejing. Regulation of skeletal myogenesis by the mTOR signaling network.

Degree: PhD, 4094, 2012, University of Illinois – Urbana-Champaign

 Skeletal muscle is composed of post-mitotic multinucleated myofibers. During embryonic skeletal myogenesis, cells in somites commit to myogenic lineage and differentiate into myoblasts, which then… (more)

Subjects/Keywords: mTOR; myogenesis; myoblast differentiation; microRNA; miRNA; mammalian target of rapamycin (mTOR); Ribonucleic acid (RNA)

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APA (6th Edition):

Ge, Y. (2012). Regulation of skeletal myogenesis by the mTOR signaling network. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/32047

Chicago Manual of Style (16th Edition):

Ge, Yejing. “Regulation of skeletal myogenesis by the mTOR signaling network.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/32047.

MLA Handbook (7th Edition):

Ge, Yejing. “Regulation of skeletal myogenesis by the mTOR signaling network.” 2012. Web. 16 Sep 2019.

Vancouver:

Ge Y. Regulation of skeletal myogenesis by the mTOR signaling network. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/32047.

Council of Science Editors:

Ge Y. Regulation of skeletal myogenesis by the mTOR signaling network. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/32047


University of Illinois – Urbana-Champaign

8. Khanna, Nidhi. Molecular mechanisms of mammalian cell survival and differentiation.

Degree: PhD, 4094, 2015, University of Illinois – Urbana-Champaign

 Cellular and developmental processes are regulated by extracellular and intracellular signals that are mediated by networks of signaling pathways. In recent years, microRNAs have also… (more)

Subjects/Keywords: NA

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APA (6th Edition):

Khanna, N. (2015). Molecular mechanisms of mammalian cell survival and differentiation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/72978

Chicago Manual of Style (16th Edition):

Khanna, Nidhi. “Molecular mechanisms of mammalian cell survival and differentiation.” 2015. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/72978.

MLA Handbook (7th Edition):

Khanna, Nidhi. “Molecular mechanisms of mammalian cell survival and differentiation.” 2015. Web. 16 Sep 2019.

Vancouver:

Khanna N. Molecular mechanisms of mammalian cell survival and differentiation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2015. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/72978.

Council of Science Editors:

Khanna N. Molecular mechanisms of mammalian cell survival and differentiation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2015. Available from: http://hdl.handle.net/2142/72978


University of Illinois – Urbana-Champaign

9. Holton, Sarah E. Systems pathology: a bottom-up approach for understanding fibroblast-epithelial interactions in breast cancer.

Degree: PhD, 0408, 2014, University of Illinois – Urbana-Champaign

 Breast cancer is prevalent both in the United States and worldwide. While both screening tests and targeted therapies are available, there are still challenges in… (more)

Subjects/Keywords: Breast cancer; Systems pathology; Stromal-epithelial interactions; Fibroblasts; Cancer; Three-dimensional cell culture; Fourier transform infrared spectroscopy (FT-IR); label-free imaging; diagnostic imaging; Breast pathology

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APA (6th Edition):

Holton, S. E. (2014). Systems pathology: a bottom-up approach for understanding fibroblast-epithelial interactions in breast cancer. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46846

Chicago Manual of Style (16th Edition):

Holton, Sarah E. “Systems pathology: a bottom-up approach for understanding fibroblast-epithelial interactions in breast cancer.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/46846.

MLA Handbook (7th Edition):

Holton, Sarah E. “Systems pathology: a bottom-up approach for understanding fibroblast-epithelial interactions in breast cancer.” 2014. Web. 16 Sep 2019.

Vancouver:

Holton SE. Systems pathology: a bottom-up approach for understanding fibroblast-epithelial interactions in breast cancer. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/46846.

Council of Science Editors:

Holton SE. Systems pathology: a bottom-up approach for understanding fibroblast-epithelial interactions in breast cancer. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46846


University of Illinois – Urbana-Champaign

10. Kaya, Hatice. Identification of molecular signaling pathways underlying human endometrial stromal cell differentiation.

Degree: PhD, 0325, 2014, University of Illinois – Urbana-Champaign

 Decidualization, the differentiation of endometrial stromal cells, is essential for a successful pregnancy. Although the steroid hormones estrogen (E) and progesterone (P) are known to… (more)

Subjects/Keywords: Human endometrial stromal cell differentiation; estrogen receptor alpha; progesterone receptor isoforms

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APA (6th Edition):

Kaya, H. (2014). Identification of molecular signaling pathways underlying human endometrial stromal cell differentiation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/46949

Chicago Manual of Style (16th Edition):

Kaya, Hatice. “Identification of molecular signaling pathways underlying human endometrial stromal cell differentiation.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/46949.

MLA Handbook (7th Edition):

Kaya, Hatice. “Identification of molecular signaling pathways underlying human endometrial stromal cell differentiation.” 2014. Web. 16 Sep 2019.

Vancouver:

Kaya H. Identification of molecular signaling pathways underlying human endometrial stromal cell differentiation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/46949.

Council of Science Editors:

Kaya H. Identification of molecular signaling pathways underlying human endometrial stromal cell differentiation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/46949


University of Illinois – Urbana-Champaign

11. Pawar, Sandeep. Molecular mechanisms regulating implantation.

Degree: PhD, 0325, 2014, University of Illinois – Urbana-Champaign

 Implantation, a critical early event during pregnancy, is a three stage process. It starts with apposition and adhesion of the blastocyst to a receptive uterine… (more)

Subjects/Keywords: Decidualization; Implantation; Steroid; Epithelial-Stromal interaction; Pregnancy; Angiogenesis

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APA (6th Edition):

Pawar, S. (2014). Molecular mechanisms regulating implantation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/49759

Chicago Manual of Style (16th Edition):

Pawar, Sandeep. “Molecular mechanisms regulating implantation.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/49759.

MLA Handbook (7th Edition):

Pawar, Sandeep. “Molecular mechanisms regulating implantation.” 2014. Web. 16 Sep 2019.

Vancouver:

Pawar S. Molecular mechanisms regulating implantation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/49759.

Council of Science Editors:

Pawar S. Molecular mechanisms regulating implantation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/49759


University of Illinois – Urbana-Champaign

12. Dietrich, Alicia. Role of estrogen receptor α and oxidative stress response proteins in the central nervous system.

Degree: PhD, 0325, 2014, University of Illinois – Urbana-Champaign

 Cellular metabolism results in the production of reactive oxygen species (ROS) as byproducts and can damage proteins, lipids, and DNA. Cells utilize a number of… (more)

Subjects/Keywords: Oxidative stress; Estrogen receptor α; Cu/Zn superoxide dismutase; Amyotrophic lateral sclerosis; Apurinic endonuclease 1; Neuroprotection; Hypoxia; Estrogen

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APA (6th Edition):

Dietrich, A. (2014). Role of estrogen receptor α and oxidative stress response proteins in the central nervous system. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/50567

Chicago Manual of Style (16th Edition):

Dietrich, Alicia. “Role of estrogen receptor α and oxidative stress response proteins in the central nervous system.” 2014. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/50567.

MLA Handbook (7th Edition):

Dietrich, Alicia. “Role of estrogen receptor α and oxidative stress response proteins in the central nervous system.” 2014. Web. 16 Sep 2019.

Vancouver:

Dietrich A. Role of estrogen receptor α and oxidative stress response proteins in the central nervous system. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/50567.

Council of Science Editors:

Dietrich A. Role of estrogen receptor α and oxidative stress response proteins in the central nervous system. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2014. Available from: http://hdl.handle.net/2142/50567


University of Illinois – Urbana-Champaign

13. Carroll, Vincent. I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens.

Degree: PhD, Chemistry, 2012, University of Illinois – Urbana-Champaign

 Molecular imaging (MI) has revolutionized the visualization of complex biochemical processes in normal physiology and diseased states. Although still in its infancy, the data generated… (more)

Subjects/Keywords: 2-fluoroestradiol; estrogen dendrimer conjugate; estrogen receptor; fluorine-18

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APA (6th Edition):

Carroll, V. (2012). I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95662

Chicago Manual of Style (16th Edition):

Carroll, Vincent. “I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/95662.

MLA Handbook (7th Edition):

Carroll, Vincent. “I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens.” 2012. Web. 16 Sep 2019.

Vancouver:

Carroll V. I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/95662.

Council of Science Editors:

Carroll V. I. Development of novel silicon precursors for rapid and efficient radiofluorination reactions: synthesis and biological evaluation of a 18f-labelled estrogen dendrimer conjugate II. Other studies on 18f-labelled estrogens. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/95662


University of Illinois – Urbana-Champaign

14. Ramathal, Cyril Y. Analysis of the role of the transcription factor C/EBPβ in controlling uterine functions during early pregnancy.

Degree: PhD, 4094, 2010, University of Illinois – Urbana-Champaign

 Embryo implantation into the endometrium is a complex biological process involving the integration of steroid hormone signaling, endometrial tissue remodeling and maternal- fetal communications. A… (more)

Subjects/Keywords: Implantation; Infertility; decidualization; embryo; uterus; endometrium; estrogen; progesterone; Extracellular Matrix (ECM)

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APA (6th Edition):

Ramathal, C. Y. (2010). Analysis of the role of the transcription factor C/EBPβ in controlling uterine functions during early pregnancy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15569

Chicago Manual of Style (16th Edition):

Ramathal, Cyril Y. “Analysis of the role of the transcription factor C/EBPβ in controlling uterine functions during early pregnancy.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/15569.

MLA Handbook (7th Edition):

Ramathal, Cyril Y. “Analysis of the role of the transcription factor C/EBPβ in controlling uterine functions during early pregnancy.” 2010. Web. 16 Sep 2019.

Vancouver:

Ramathal CY. Analysis of the role of the transcription factor C/EBPβ in controlling uterine functions during early pregnancy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/15569.

Council of Science Editors:

Ramathal CY. Analysis of the role of the transcription factor C/EBPβ in controlling uterine functions during early pregnancy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15569


University of Illinois – Urbana-Champaign

15. Wang, Wei. Analysis of the role of the transcription factor-C/EBPβ in implantation.

Degree: PhD, 0325, 2010, University of Illinois – Urbana-Champaign

 During early pregnancy, the concerted actions of the maternal steroid hormones, estrogen and progesterone, promote a unique process known as decidualization, which involves extensive proliferation… (more)

Subjects/Keywords: CCAAT-Enhancer-Binding Protein-beta; pregnancy; Implantation; decidualization; hormone; estrogen; progesterone; uterus; cell proliferation; cell differentiation; gene expression regulation; Female; Mice; Human

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APA (6th Edition):

Wang, W. (2010). Analysis of the role of the transcription factor-C/EBPβ in implantation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15586

Chicago Manual of Style (16th Edition):

Wang, Wei. “Analysis of the role of the transcription factor-C/EBPβ in implantation.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/15586.

MLA Handbook (7th Edition):

Wang, Wei. “Analysis of the role of the transcription factor-C/EBPβ in implantation.” 2010. Web. 16 Sep 2019.

Vancouver:

Wang W. Analysis of the role of the transcription factor-C/EBPβ in implantation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/15586.

Council of Science Editors:

Wang W. Analysis of the role of the transcription factor-C/EBPβ in implantation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15586


University of Illinois – Urbana-Champaign

16. Hu, Yan. Changes in large-scale chromatin structure and dynamics of BAC transgenes during transcriptional activation.

Degree: PhD, 4094, 2010, University of Illinois – Urbana-Champaign

 Mounting evidence suggests that the eukaryotic cell nucleus is a dynamic and complex structure, and that changes in large-scale chromatin structure play an important role… (more)

Subjects/Keywords: large-scale chromatin structure; Bacterial artificial chromosome (BAC); SC-35 domains; nuclear speckle; immunogold; transcription; Heat shock protein 70 (Hsp70) promoter; promoter specificity; heat shock; cadmium

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APA (6th Edition):

Hu, Y. (2010). Changes in large-scale chromatin structure and dynamics of BAC transgenes during transcriptional activation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15600

Chicago Manual of Style (16th Edition):

Hu, Yan. “Changes in large-scale chromatin structure and dynamics of BAC transgenes during transcriptional activation.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/15600.

MLA Handbook (7th Edition):

Hu, Yan. “Changes in large-scale chromatin structure and dynamics of BAC transgenes during transcriptional activation.” 2010. Web. 16 Sep 2019.

Vancouver:

Hu Y. Changes in large-scale chromatin structure and dynamics of BAC transgenes during transcriptional activation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/15600.

Council of Science Editors:

Hu Y. Changes in large-scale chromatin structure and dynamics of BAC transgenes during transcriptional activation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15600


University of Illinois – Urbana-Champaign

17. Cherian, Milu. Small molecule inhibitors of steroid receptors for breast and prostate cancer.

Degree: PhD, 0325, 2012, University of Illinois – Urbana-Champaign

 Steroid hormone receptors play a critical role in the growth and progression of hormone-dependent cancers. This thesis aimed at identifying and characterizing new chemical entities… (more)

Subjects/Keywords: Androgen receptor; Prostate cancer; 1-(3-(2-chlorophenoxy)propyl)-1H-indole-3-carbonitrile (CPIC); Drug discovery; Small molecule; High throughput screening

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APA (6th Edition):

Cherian, M. (2012). Small molecule inhibitors of steroid receptors for breast and prostate cancer. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/34580

Chicago Manual of Style (16th Edition):

Cherian, Milu. “Small molecule inhibitors of steroid receptors for breast and prostate cancer.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/34580.

MLA Handbook (7th Edition):

Cherian, Milu. “Small molecule inhibitors of steroid receptors for breast and prostate cancer.” 2012. Web. 16 Sep 2019.

Vancouver:

Cherian M. Small molecule inhibitors of steroid receptors for breast and prostate cancer. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/34580.

Council of Science Editors:

Cherian M. Small molecule inhibitors of steroid receptors for breast and prostate cancer. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/34580

18. Chen, Congcong. Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells.

Degree: PhD, Molecular & Integrative Physi, 2016, University of Illinois – Urbana-Champaign

 Androgen receptor (AR) signaling is crucial to the development, growth, and homeostasis of the prostate gland, and its dysregulation mediates common prostate pathologies, including benign… (more)

Subjects/Keywords: Androgen Receptor; Prostate; Homeostasis; Prostate Cancer; Proliferation; Growth Suppression; Cell Cycle; Cell Death; Apoptosis; Stress; Autophagy

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APA (6th Edition):

Chen, C. (2016). Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95312

Chicago Manual of Style (16th Edition):

Chen, Congcong. “Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/95312.

MLA Handbook (7th Edition):

Chen, Congcong. “Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells.” 2016. Web. 16 Sep 2019.

Vancouver:

Chen C. Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/95312.

Council of Science Editors:

Chen C. Androgen receptor-mediated growth suppression and apoptosis of human prostate epithelial cells. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95312

19. Lee, Jiyoung. Gene selective regulation by hepatic Farnesoid x receptor (fxr) in health and disease.

Degree: PhD, 0325, 2011, University of Illinois – Urbana-Champaign

 Metabolic syndrome is a clustered condition including obesity, insulin resistance, hypertension, dyslipidemia, and liver steatosis. The incidence of metabolic syndrome and the accompanying risk of… (more)

Subjects/Keywords: Hepatic bile acid nuclear receptor; Farnesoid X Receptor (FXR); bile acid; diet-induced metabolic disease; obesity; SIRT1; miR-34a; ChIP-Sequencing (ChIP-seq)

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APA (6th Edition):

Lee, J. (2011). Gene selective regulation by hepatic Farnesoid x receptor (fxr) in health and disease. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24437

Chicago Manual of Style (16th Edition):

Lee, Jiyoung. “Gene selective regulation by hepatic Farnesoid x receptor (fxr) in health and disease.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/24437.

MLA Handbook (7th Edition):

Lee, Jiyoung. “Gene selective regulation by hepatic Farnesoid x receptor (fxr) in health and disease.” 2011. Web. 16 Sep 2019.

Vancouver:

Lee J. Gene selective regulation by hepatic Farnesoid x receptor (fxr) in health and disease. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/24437.

Council of Science Editors:

Lee J. Gene selective regulation by hepatic Farnesoid x receptor (fxr) in health and disease. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24437

20. Aninye, Irene. Small molecule inhibitors: novel probes of progesterone receptor action.

Degree: PhD, 0325, 2012, University of Illinois – Urbana-Champaign

 The progesterone receptor (PR) is an important member of the nuclear receptor superfamily of transcription regulatory proteins. It plays vital roles in a diverse set… (more)

Subjects/Keywords: progesterone; steroid receptor; small molecule inhibitor; theophylline; structure activity relationship

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APA (6th Edition):

Aninye, I. (2012). Small molecule inhibitors: novel probes of progesterone receptor action. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/31017

Chicago Manual of Style (16th Edition):

Aninye, Irene. “Small molecule inhibitors: novel probes of progesterone receptor action.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/31017.

MLA Handbook (7th Edition):

Aninye, Irene. “Small molecule inhibitors: novel probes of progesterone receptor action.” 2012. Web. 16 Sep 2019.

Vancouver:

Aninye I. Small molecule inhibitors: novel probes of progesterone receptor action. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/31017.

Council of Science Editors:

Aninye I. Small molecule inhibitors: novel probes of progesterone receptor action. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/31017

21. Anandan, Lavanya. Role of Cuzd1 in mammary gland development and tumorigenesis.

Degree: PhD, 0325, 2012, University of Illinois – Urbana-Champaign

 The mechanisms by which the pathways regulated by the steroid hormones and the epidermal growth factor (EGF) family control mammary development are unclear. We have… (more)

Subjects/Keywords: CUB and zona pellucida-like domain containing protein-1 (CUZD1); mammary gland; proliferation; tumorigenesis; breast cancer

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APA (6th Edition):

Anandan, L. (2012). Role of Cuzd1 in mammary gland development and tumorigenesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29561

Chicago Manual of Style (16th Edition):

Anandan, Lavanya. “Role of Cuzd1 in mammary gland development and tumorigenesis.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/29561.

MLA Handbook (7th Edition):

Anandan, Lavanya. “Role of Cuzd1 in mammary gland development and tumorigenesis.” 2012. Web. 16 Sep 2019.

Vancouver:

Anandan L. Role of Cuzd1 in mammary gland development and tumorigenesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/29561.

Council of Science Editors:

Anandan L. Role of Cuzd1 in mammary gland development and tumorigenesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29561

22. Moran, Tyler B. Uncovering novel actions of numb and aryl hydrocarbon receptor in the pituitary.

Degree: PhD, 0325, 2011, University of Illinois – Urbana-Champaign

 Many physiological responses are regulated by the pituitary including, but not limited to, growth, metabolism, response to stress, and fertility. These responses in the anterior… (more)

Subjects/Keywords: Numb; pituitary; Notch; Aryl hydrocarbon receptor (AhR or AHR)

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APA (6th Edition):

Moran, T. B. (2011). Uncovering novel actions of numb and aryl hydrocarbon receptor in the pituitary. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/24432

Chicago Manual of Style (16th Edition):

Moran, Tyler B. “Uncovering novel actions of numb and aryl hydrocarbon receptor in the pituitary.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/24432.

MLA Handbook (7th Edition):

Moran, Tyler B. “Uncovering novel actions of numb and aryl hydrocarbon receptor in the pituitary.” 2011. Web. 16 Sep 2019.

Vancouver:

Moran TB. Uncovering novel actions of numb and aryl hydrocarbon receptor in the pituitary. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/24432.

Council of Science Editors:

Moran TB. Uncovering novel actions of numb and aryl hydrocarbon receptor in the pituitary. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/24432


University of Illinois – Urbana-Champaign

23. Fang, Sungsoon. The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling.

Degree: PhD, Molecular & Integrative Physiology, 2008, University of Illinois – Urbana-Champaign

 Bile acids, the end-product of cholesterol catabolism, are important for absorption and solubilization of lipids in the intestine because of their detergent properties. In addition… (more)

Subjects/Keywords: Bile acids; Bile acid signaling; Farnesoid X receptor (FXR); Small heterodimer partner (SHP)

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APA (6th Edition):

Fang, S. (2008). The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/47090

Chicago Manual of Style (16th Edition):

Fang, Sungsoon. “The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling.” 2008. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 16, 2019. http://hdl.handle.net/2142/47090.

MLA Handbook (7th Edition):

Fang, Sungsoon. “The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling.” 2008. Web. 16 Sep 2019.

Vancouver:

Fang S. The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2008. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/2142/47090.

Council of Science Editors:

Fang S. The roles of orphan nuclear receptors, SHP and FXR, and their cofactors in bile acid signaling. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2008. Available from: http://hdl.handle.net/2142/47090

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