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You searched for subject:(Estrogen receptor). Showing records 1 – 30 of 472 total matches.

[1] [2] [3] [4] [5] … [16]

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Georgia Tech

1. Walker, Christopher L. Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application.

Degree: PhD, Chemistry and Biochemistry, 2019, Georgia Tech

 Nuclear receptors are ligand activated transcription factors that are widely distributed throughout the mammalians. There are 48 known human nuclear receptors within the body located… (more)

Subjects/Keywords: Estrogen receptor

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APA (6th Edition):

Walker, C. L. (2019). Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61211

Chicago Manual of Style (16th Edition):

Walker, Christopher L. “Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application.” 2019. Doctoral Dissertation, Georgia Tech. Accessed November 27, 2020. http://hdl.handle.net/1853/61211.

MLA Handbook (7th Edition):

Walker, Christopher L. “Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application.” 2019. Web. 27 Nov 2020.

Vancouver:

Walker CL. Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1853/61211.

Council of Science Editors:

Walker CL. Green fluorescent protein inspired chromophore as estrogen receptor agonist-synthesis, biological evaluations and cellular application. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/61211


Rutgers University

2. Yasrebi, Ali, 1987-. ERE-independent ERα signalling in feeding and exploratory behaviors.

Degree: MS, Endocrinology and Animal Biosciences, 2019, Rutgers University

 The reproductive steroid hormone, 17β-estradiol (E2), controls feeding and exploratory behaviors associated with mood disorders. The loss of circulating E2 puts menopausal women at an… (more)

Subjects/Keywords: Estrogen receptor alpha; Estrogen  – Receptors

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APA (6th Edition):

Yasrebi, Ali, 1. (2019). ERE-independent ERα signalling in feeding and exploratory behaviors. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/62067/

Chicago Manual of Style (16th Edition):

Yasrebi, Ali, 1987-. “ERE-independent ERα signalling in feeding and exploratory behaviors.” 2019. Masters Thesis, Rutgers University. Accessed November 27, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/62067/.

MLA Handbook (7th Edition):

Yasrebi, Ali, 1987-. “ERE-independent ERα signalling in feeding and exploratory behaviors.” 2019. Web. 27 Nov 2020.

Vancouver:

Yasrebi, Ali 1. ERE-independent ERα signalling in feeding and exploratory behaviors. [Internet] [Masters thesis]. Rutgers University; 2019. [cited 2020 Nov 27]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/62067/.

Council of Science Editors:

Yasrebi, Ali 1. ERE-independent ERα signalling in feeding and exploratory behaviors. [Masters Thesis]. Rutgers University; 2019. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/62067/

3. Magruder, Hilary. Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression.

Degree: PhD, Pathobiology, 2014, Brown University

 Stimulation of estrogen receptor (ER)-negative human breast cancer cells with 17β-estradiol (E2β) results in fibronectin (FN) matrix assembly and transactivation of the epidermal growth factor… (more)

Subjects/Keywords: estrogen receptor (ER)

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APA (6th Edition):

Magruder, H. (2014). Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:386260/

Chicago Manual of Style (16th Edition):

Magruder, Hilary. “Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression.” 2014. Doctoral Dissertation, Brown University. Accessed November 27, 2020. https://repository.library.brown.edu/studio/item/bdr:386260/.

MLA Handbook (7th Edition):

Magruder, Hilary. “Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression.” 2014. Web. 27 Nov 2020.

Vancouver:

Magruder H. Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression. [Internet] [Doctoral dissertation]. Brown University; 2014. [cited 2020 Nov 27]. Available from: https://repository.library.brown.edu/studio/item/bdr:386260/.

Council of Science Editors:

Magruder H. Signaling Effectors Required for G Protein-Coupled Estrogen Receptor-, GPER, Induced Events Associated with Breast Cancer Progression. [Doctoral Dissertation]. Brown University; 2014. Available from: https://repository.library.brown.edu/studio/item/bdr:386260/


University of Illinois – Urbana-Champaign

4. Parent, Alexander A. Second-site inhibitors of the estrogen and androgen hormone receptors.

Degree: PhD, 0335, 2012, University of Illinois – Urbana-Champaign

 The estrogen and androgen receptors are members of the nuclear hormone receptor protein superfamily and play an important role in the development of primary and… (more)

Subjects/Keywords: estrogen receptor; androgen receptor; inhibitor; nuclear receptor

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APA (6th Edition):

Parent, A. A. (2012). Second-site inhibitors of the estrogen and androgen hormone receptors. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29523

Chicago Manual of Style (16th Edition):

Parent, Alexander A. “Second-site inhibitors of the estrogen and androgen hormone receptors.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 27, 2020. http://hdl.handle.net/2142/29523.

MLA Handbook (7th Edition):

Parent, Alexander A. “Second-site inhibitors of the estrogen and androgen hormone receptors.” 2012. Web. 27 Nov 2020.

Vancouver:

Parent AA. Second-site inhibitors of the estrogen and androgen hormone receptors. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2142/29523.

Council of Science Editors:

Parent AA. Second-site inhibitors of the estrogen and androgen hormone receptors. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29523


Boston University

5. Koomson, Jacqueline Nyarkoa. The role of estrogen receptors alpha and beta in the development of uterine leiomyomas.

Degree: MS, Medical Sciences, 2017, Boston University

 Uterine leiomyomas are benign tumors within the uterus, where patients present with symptoms such as abnormal bleeding, urinary retention, and pelvic pressure. The exact etiology… (more)

Subjects/Keywords: Medicine; Estrogen; Estrogen receptor alpha; Estrogen receptor beta; Receptor-mediated therapies; Uterine fibroids; Uterine leiomyoma

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APA (6th Edition):

Koomson, J. N. (2017). The role of estrogen receptors alpha and beta in the development of uterine leiomyomas. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/23835

Chicago Manual of Style (16th Edition):

Koomson, Jacqueline Nyarkoa. “The role of estrogen receptors alpha and beta in the development of uterine leiomyomas.” 2017. Masters Thesis, Boston University. Accessed November 27, 2020. http://hdl.handle.net/2144/23835.

MLA Handbook (7th Edition):

Koomson, Jacqueline Nyarkoa. “The role of estrogen receptors alpha and beta in the development of uterine leiomyomas.” 2017. Web. 27 Nov 2020.

Vancouver:

Koomson JN. The role of estrogen receptors alpha and beta in the development of uterine leiomyomas. [Internet] [Masters thesis]. Boston University; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2144/23835.

Council of Science Editors:

Koomson JN. The role of estrogen receptors alpha and beta in the development of uterine leiomyomas. [Masters Thesis]. Boston University; 2017. Available from: http://hdl.handle.net/2144/23835


Cornell University

6. Melville, Katherine. Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading.

Degree: PhD, Biomedical Engineering, 2014, Cornell University

 Decreased bioavailable estrogen levels are a major cause of bone loss in postmenopausal women, but sex hormones are important regulators of bone mass in both… (more)

Subjects/Keywords: estrogen receptor alpha; bone; loading

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APA (6th Edition):

Melville, K. (2014). Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/38857

Chicago Manual of Style (16th Edition):

Melville, Katherine. “Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading.” 2014. Doctoral Dissertation, Cornell University. Accessed November 27, 2020. http://hdl.handle.net/1813/38857.

MLA Handbook (7th Edition):

Melville, Katherine. “Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading.” 2014. Web. 27 Nov 2020.

Vancouver:

Melville K. Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1813/38857.

Council of Science Editors:

Melville K. Estrogen Receptor Alpha In Osteoblasts Mediates Bone Mass And Bone’S Response To In Vivo Loading. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/38857


University of Otago

7. Tran, Khanh Bao. Synthetic Cannabinoids as a Novel Treatment for Triple Negative Breast Cancer .

Degree: 2012, University of Otago

 Approximately one in five breast cancer patients exhibits triple negative tumors that are characterized by the lack of estrogen receptor (ER), progesterone receptor and HER2.… (more)

Subjects/Keywords: cannabinoids; breast cancer; estrogen receptor

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APA (6th Edition):

Tran, K. B. (2012). Synthetic Cannabinoids as a Novel Treatment for Triple Negative Breast Cancer . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/2292

Chicago Manual of Style (16th Edition):

Tran, Khanh Bao. “Synthetic Cannabinoids as a Novel Treatment for Triple Negative Breast Cancer .” 2012. Masters Thesis, University of Otago. Accessed November 27, 2020. http://hdl.handle.net/10523/2292.

MLA Handbook (7th Edition):

Tran, Khanh Bao. “Synthetic Cannabinoids as a Novel Treatment for Triple Negative Breast Cancer .” 2012. Web. 27 Nov 2020.

Vancouver:

Tran KB. Synthetic Cannabinoids as a Novel Treatment for Triple Negative Breast Cancer . [Internet] [Masters thesis]. University of Otago; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10523/2292.

Council of Science Editors:

Tran KB. Synthetic Cannabinoids as a Novel Treatment for Triple Negative Breast Cancer . [Masters Thesis]. University of Otago; 2012. Available from: http://hdl.handle.net/10523/2292


Northeastern University

8. Gajadeera, Nisal. Design, Synthesis And In Vitro Investigations Of Novel Fluorescently Labeled Steroids.

Degree: MS, Department of Chemistry and Chemical Biology, 2018, Northeastern University

 Breast cancer is the most common cancer among women, accounting for nearly third of all the diagnosed cancers. According to the American cancer society, over… (more)

Subjects/Keywords: Estrogen receptor; Imaging agent; Chemistry

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APA (6th Edition):

Gajadeera, N. (2018). Design, Synthesis And In Vitro Investigations Of Novel Fluorescently Labeled Steroids. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20316349

Chicago Manual of Style (16th Edition):

Gajadeera, Nisal. “Design, Synthesis And In Vitro Investigations Of Novel Fluorescently Labeled Steroids.” 2018. Masters Thesis, Northeastern University. Accessed November 27, 2020. http://hdl.handle.net/2047/D20316349.

MLA Handbook (7th Edition):

Gajadeera, Nisal. “Design, Synthesis And In Vitro Investigations Of Novel Fluorescently Labeled Steroids.” 2018. Web. 27 Nov 2020.

Vancouver:

Gajadeera N. Design, Synthesis And In Vitro Investigations Of Novel Fluorescently Labeled Steroids. [Internet] [Masters thesis]. Northeastern University; 2018. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2047/D20316349.

Council of Science Editors:

Gajadeera N. Design, Synthesis And In Vitro Investigations Of Novel Fluorescently Labeled Steroids. [Masters Thesis]. Northeastern University; 2018. Available from: http://hdl.handle.net/2047/D20316349


University of Houston

9. Son, Jieun 1985-. Mechanism of Estrogen Receptor Alpha in Cervical Carcinogenesis.

Degree: PhD, Cell and Molecular Biology, 2017, University of Houston

 Most cervical cancers are associated with high-risk human papillomaviruses (HPVs). HPVs display tumorigenic functions in host cells mainly through viral oncogenes E6 and E7 that… (more)

Subjects/Keywords: Estrogen receptor alpha; Cervical cancer

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APA (6th Edition):

Son, J. 1. (2017). Mechanism of Estrogen Receptor Alpha in Cervical Carcinogenesis. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/4602

Chicago Manual of Style (16th Edition):

Son, Jieun 1985-. “Mechanism of Estrogen Receptor Alpha in Cervical Carcinogenesis.” 2017. Doctoral Dissertation, University of Houston. Accessed November 27, 2020. http://hdl.handle.net/10657/4602.

MLA Handbook (7th Edition):

Son, Jieun 1985-. “Mechanism of Estrogen Receptor Alpha in Cervical Carcinogenesis.” 2017. Web. 27 Nov 2020.

Vancouver:

Son J1. Mechanism of Estrogen Receptor Alpha in Cervical Carcinogenesis. [Internet] [Doctoral dissertation]. University of Houston; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10657/4602.

Council of Science Editors:

Son J1. Mechanism of Estrogen Receptor Alpha in Cervical Carcinogenesis. [Doctoral Dissertation]. University of Houston; 2017. Available from: http://hdl.handle.net/10657/4602


University of Manitoba

10. Chooniedass, Shilpa. The role of the newly discovered steroid receptor RNA activator protein (SRAP) in the estrogen signaling pathway and its implication in breast cancer.

Degree: Biochemistry and Medical Genetics, 2011, University of Manitoba

 In 1999, the discovery of the Steroid Receptor RNA Activator (SRA) was unprecedented in the field of steroid receptor co-regulator research. It was the first… (more)

Subjects/Keywords: steoid receptor RNA activator; estrogen receptor

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APA (6th Edition):

Chooniedass, S. (2011). The role of the newly discovered steroid receptor RNA activator protein (SRAP) in the estrogen signaling pathway and its implication in breast cancer. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4421

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chooniedass, Shilpa. “The role of the newly discovered steroid receptor RNA activator protein (SRAP) in the estrogen signaling pathway and its implication in breast cancer.” 2011. Thesis, University of Manitoba. Accessed November 27, 2020. http://hdl.handle.net/1993/4421.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chooniedass, Shilpa. “The role of the newly discovered steroid receptor RNA activator protein (SRAP) in the estrogen signaling pathway and its implication in breast cancer.” 2011. Web. 27 Nov 2020.

Vancouver:

Chooniedass S. The role of the newly discovered steroid receptor RNA activator protein (SRAP) in the estrogen signaling pathway and its implication in breast cancer. [Internet] [Thesis]. University of Manitoba; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1993/4421.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chooniedass S. The role of the newly discovered steroid receptor RNA activator protein (SRAP) in the estrogen signaling pathway and its implication in breast cancer. [Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4421

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Rochester

11. Hsu, Iawen. The Roles of Estrogen Receptors in the Bladder Cancer Development.

Degree: PhD, 2013, University of Rochester

 Early studies documented the existence of sexual dimorphism in bladder cancer occurrence and progression with higher bladder cancer incidence in males than females. However, the… (more)

Subjects/Keywords: Estrogen Receptor Alpha; Estrogen Receptor Beta; MCM5; Bladder Cancer BBN; Inpp4β

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APA (6th Edition):

Hsu, I. (2013). The Roles of Estrogen Receptors in the Bladder Cancer Development. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27302

Chicago Manual of Style (16th Edition):

Hsu, Iawen. “The Roles of Estrogen Receptors in the Bladder Cancer Development.” 2013. Doctoral Dissertation, University of Rochester. Accessed November 27, 2020. http://hdl.handle.net/1802/27302.

MLA Handbook (7th Edition):

Hsu, Iawen. “The Roles of Estrogen Receptors in the Bladder Cancer Development.” 2013. Web. 27 Nov 2020.

Vancouver:

Hsu I. The Roles of Estrogen Receptors in the Bladder Cancer Development. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1802/27302.

Council of Science Editors:

Hsu I. The Roles of Estrogen Receptors in the Bladder Cancer Development. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27302


University of Toronto

12. Tan, Susanna Shu Xian. Characterizing the Role of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible poly-ADP-ribose Polymerase (TIPARP) in Estrogen Receptor Signalling.

Degree: 2016, University of Toronto

Estrogens exert their effects by activating estrogen receptor alpha (ERα) and beta (ERβ). A number of different co-regulator proteins regulate the activities of both receptors.… (more)

Subjects/Keywords: Estrogen; Estrogen Receptor; Nuclear transcription factors; Receptor Signalling; TIPARP; 0307

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APA (6th Edition):

Tan, S. S. X. (2016). Characterizing the Role of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible poly-ADP-ribose Polymerase (TIPARP) in Estrogen Receptor Signalling. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76045

Chicago Manual of Style (16th Edition):

Tan, Susanna Shu Xian. “Characterizing the Role of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible poly-ADP-ribose Polymerase (TIPARP) in Estrogen Receptor Signalling.” 2016. Masters Thesis, University of Toronto. Accessed November 27, 2020. http://hdl.handle.net/1807/76045.

MLA Handbook (7th Edition):

Tan, Susanna Shu Xian. “Characterizing the Role of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible poly-ADP-ribose Polymerase (TIPARP) in Estrogen Receptor Signalling.” 2016. Web. 27 Nov 2020.

Vancouver:

Tan SSX. Characterizing the Role of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible poly-ADP-ribose Polymerase (TIPARP) in Estrogen Receptor Signalling. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1807/76045.

Council of Science Editors:

Tan SSX. Characterizing the Role of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)-inducible poly-ADP-ribose Polymerase (TIPARP) in Estrogen Receptor Signalling. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76045


Univerzitet u Beogradu

13. Božović, Ana M., 1977-. Metilovanje promotora i ekspresija estrogenskog receptora beta (ERß) u invazivnim karcinomima dojke.

Degree: Biološki fakultet, 2014, Univerzitet u Beogradu

Biologija - Molekularna genetika kancera / Biology - Molecular genetics of cancer

Invazivni karcinom dojke je najčešći kancer kod žena. Pored genetičkih i epigenetički faktori… (more)

Subjects/Keywords: Breast cancer; estrogen receptor alpha; estrogen receptor beta; progesterone receptor; methylation; quantitative PCR

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APA (6th Edition):

Božović, Ana M., 1. (2014). Metilovanje promotora i ekspresija estrogenskog receptora beta (ERß) u invazivnim karcinomima dojke. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:7126/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Božović, Ana M., 1977-. “Metilovanje promotora i ekspresija estrogenskog receptora beta (ERß) u invazivnim karcinomima dojke.” 2014. Thesis, Univerzitet u Beogradu. Accessed November 27, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:7126/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Božović, Ana M., 1977-. “Metilovanje promotora i ekspresija estrogenskog receptora beta (ERß) u invazivnim karcinomima dojke.” 2014. Web. 27 Nov 2020.

Vancouver:

Božović, Ana M. 1. Metilovanje promotora i ekspresija estrogenskog receptora beta (ERß) u invazivnim karcinomima dojke. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2020 Nov 27]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7126/bdef:Content/get.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Božović, Ana M. 1. Metilovanje promotora i ekspresija estrogenskog receptora beta (ERß) u invazivnim karcinomima dojke. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7126/bdef:Content/get

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Guelph

14. Ervin, Kelsy. The role of specific estrogen receptors in mediating rapid estrogenic improvements of social learning in female mice.

Degree: MS, Department of Psychology, 2014, University of Guelph

 Social learning is a process by which an animal gains information from another; however much of the research on estrogens effects on learning focuses on… (more)

Subjects/Keywords: estradiol; social transmission of food preference; estrogen receptor alpha; estrogen receptor beta; G protein-coupled estrogen receptor; GPER; GPR30

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APA (6th Edition):

Ervin, K. (2014). The role of specific estrogen receptors in mediating rapid estrogenic improvements of social learning in female mice. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7818

Chicago Manual of Style (16th Edition):

Ervin, Kelsy. “The role of specific estrogen receptors in mediating rapid estrogenic improvements of social learning in female mice.” 2014. Masters Thesis, University of Guelph. Accessed November 27, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7818.

MLA Handbook (7th Edition):

Ervin, Kelsy. “The role of specific estrogen receptors in mediating rapid estrogenic improvements of social learning in female mice.” 2014. Web. 27 Nov 2020.

Vancouver:

Ervin K. The role of specific estrogen receptors in mediating rapid estrogenic improvements of social learning in female mice. [Internet] [Masters thesis]. University of Guelph; 2014. [cited 2020 Nov 27]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7818.

Council of Science Editors:

Ervin K. The role of specific estrogen receptors in mediating rapid estrogenic improvements of social learning in female mice. [Masters Thesis]. University of Guelph; 2014. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/7818


Cornell University

15. Hah, Nasun. Signal Regulated Gene Expression: Defining The Effects Of Estrogen Signaling Through Genomic And Proteomic Analyses.

Degree: PhD, Biochemistry, 2011, Cornell University

 Estrogens play crucial roles in regulating gene expression in physiological and disease states. Estrogens acts through estrogen receptors (ERs) and their binding sites in genomic… (more)

Subjects/Keywords: estrogen; estrogen receptor; GRO-seq; swi/snf; baf57; baf180; silac; proteomic; enhancer; edc; estrogen signaling

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APA (6th Edition):

Hah, N. (2011). Signal Regulated Gene Expression: Defining The Effects Of Estrogen Signaling Through Genomic And Proteomic Analyses. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33589

Chicago Manual of Style (16th Edition):

Hah, Nasun. “Signal Regulated Gene Expression: Defining The Effects Of Estrogen Signaling Through Genomic And Proteomic Analyses.” 2011. Doctoral Dissertation, Cornell University. Accessed November 27, 2020. http://hdl.handle.net/1813/33589.

MLA Handbook (7th Edition):

Hah, Nasun. “Signal Regulated Gene Expression: Defining The Effects Of Estrogen Signaling Through Genomic And Proteomic Analyses.” 2011. Web. 27 Nov 2020.

Vancouver:

Hah N. Signal Regulated Gene Expression: Defining The Effects Of Estrogen Signaling Through Genomic And Proteomic Analyses. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1813/33589.

Council of Science Editors:

Hah N. Signal Regulated Gene Expression: Defining The Effects Of Estrogen Signaling Through Genomic And Proteomic Analyses. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33589


Vanderbilt University

16. Pruitt, Freddie Lee. A role for estrogen receptor and the estrogen-regulated protease cathepsin D in stromally-driven prostatic carcinogenesis.

Degree: PhD, Cancer Biology, 2013, Vanderbilt University

 Stromal-epithelial interactions are important in both prostate development and cancer. Stromal changes have been shown to be powerful prognostic indicators of prostate cancer progression and… (more)

Subjects/Keywords: Stroma; microenvironment; estrogen receptor; cathepsin D

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APA (6th Edition):

Pruitt, F. L. (2013). A role for estrogen receptor and the estrogen-regulated protease cathepsin D in stromally-driven prostatic carcinogenesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12683

Chicago Manual of Style (16th Edition):

Pruitt, Freddie Lee. “A role for estrogen receptor and the estrogen-regulated protease cathepsin D in stromally-driven prostatic carcinogenesis.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed November 27, 2020. http://hdl.handle.net/1803/12683.

MLA Handbook (7th Edition):

Pruitt, Freddie Lee. “A role for estrogen receptor and the estrogen-regulated protease cathepsin D in stromally-driven prostatic carcinogenesis.” 2013. Web. 27 Nov 2020.

Vancouver:

Pruitt FL. A role for estrogen receptor and the estrogen-regulated protease cathepsin D in stromally-driven prostatic carcinogenesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1803/12683.

Council of Science Editors:

Pruitt FL. A role for estrogen receptor and the estrogen-regulated protease cathepsin D in stromally-driven prostatic carcinogenesis. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/12683


Vanderbilt University

17. Ludwik, Katarzyna Anna. RSKy Business in the Mammary Gland.

Degree: PhD, Pathology, 2018, Vanderbilt University

 The family of ribosomal S6 Ser/Thr protein kinases (RSK) controls proliferation, viability and motility and, therefore, contributes to the etiology of numerous cancers, including breast.… (more)

Subjects/Keywords: breast cancer; mammary gland; RSK2; estrogen receptor

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APA (6th Edition):

Ludwik, K. A. (2018). RSKy Business in the Mammary Gland. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11180

Chicago Manual of Style (16th Edition):

Ludwik, Katarzyna Anna. “RSKy Business in the Mammary Gland.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed November 27, 2020. http://hdl.handle.net/1803/11180.

MLA Handbook (7th Edition):

Ludwik, Katarzyna Anna. “RSKy Business in the Mammary Gland.” 2018. Web. 27 Nov 2020.

Vancouver:

Ludwik KA. RSKy Business in the Mammary Gland. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1803/11180.

Council of Science Editors:

Ludwik KA. RSKy Business in the Mammary Gland. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/11180


Texas A&M University

18. Armstrong, Cameron Michelle. The Protective Effects of Estradiol on Sporadic and Inflammation-associated Colon Cancer.

Degree: PhD, Nutrition, 2013, Texas A&M University

 Epidemiological studies suggest pre-menopausal women have a reduced risk for sporadic and inflammation-associated colon cancer compared to post-menopausal women and men. The studies presented herein… (more)

Subjects/Keywords: colon cancer; estradiol; estrogen receptor; inflammation

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APA (6th Edition):

Armstrong, C. M. (2013). The Protective Effects of Estradiol on Sporadic and Inflammation-associated Colon Cancer. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151883

Chicago Manual of Style (16th Edition):

Armstrong, Cameron Michelle. “The Protective Effects of Estradiol on Sporadic and Inflammation-associated Colon Cancer.” 2013. Doctoral Dissertation, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/151883.

MLA Handbook (7th Edition):

Armstrong, Cameron Michelle. “The Protective Effects of Estradiol on Sporadic and Inflammation-associated Colon Cancer.” 2013. Web. 27 Nov 2020.

Vancouver:

Armstrong CM. The Protective Effects of Estradiol on Sporadic and Inflammation-associated Colon Cancer. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/151883.

Council of Science Editors:

Armstrong CM. The Protective Effects of Estradiol on Sporadic and Inflammation-associated Colon Cancer. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151883


University of Ottawa

19. Boucher, Julie. Perinatal Nicotine Exposure Upregulates ERα In the Dentate Gyrus of Adult Male Rat Offspring .

Degree: 2015, University of Ottawa

 Cigarette smoking during pregnancy contributes to the development of neurological health problems in offspring. As a result, public health organizations are recommending NRT to pregnant… (more)

Subjects/Keywords: nicotine; estrogen receptor; immunohistochemistry; astrocyte; neuron

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APA (6th Edition):

Boucher, J. (2015). Perinatal Nicotine Exposure Upregulates ERα In the Dentate Gyrus of Adult Male Rat Offspring . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32957

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Boucher, Julie. “Perinatal Nicotine Exposure Upregulates ERα In the Dentate Gyrus of Adult Male Rat Offspring .” 2015. Thesis, University of Ottawa. Accessed November 27, 2020. http://hdl.handle.net/10393/32957.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Boucher, Julie. “Perinatal Nicotine Exposure Upregulates ERα In the Dentate Gyrus of Adult Male Rat Offspring .” 2015. Web. 27 Nov 2020.

Vancouver:

Boucher J. Perinatal Nicotine Exposure Upregulates ERα In the Dentate Gyrus of Adult Male Rat Offspring . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10393/32957.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Boucher J. Perinatal Nicotine Exposure Upregulates ERα In the Dentate Gyrus of Adult Male Rat Offspring . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32957

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Houston

20. -8465-3791. Defining Anti-Tumorigenic and Anti-Inflammatory Effects Mediated By Estrogen Receptor Beta In Colon Epithelial Cells.

Degree: PhD, Biology and Biochemistry, 2015, University of Houston

 Despite its slow development and our capacity for early detection using endoscopy, colorectal cancer remains the second leading cause of cancer death in the United… (more)

Subjects/Keywords: Estrogen receptor beta; Colon cancer epithelial cells

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APA (6th Edition):

-8465-3791. (2015). Defining Anti-Tumorigenic and Anti-Inflammatory Effects Mediated By Estrogen Receptor Beta In Colon Epithelial Cells. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/2018

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8465-3791. “Defining Anti-Tumorigenic and Anti-Inflammatory Effects Mediated By Estrogen Receptor Beta In Colon Epithelial Cells.” 2015. Doctoral Dissertation, University of Houston. Accessed November 27, 2020. http://hdl.handle.net/10657/2018.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-8465-3791. “Defining Anti-Tumorigenic and Anti-Inflammatory Effects Mediated By Estrogen Receptor Beta In Colon Epithelial Cells.” 2015. Web. 27 Nov 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8465-3791. Defining Anti-Tumorigenic and Anti-Inflammatory Effects Mediated By Estrogen Receptor Beta In Colon Epithelial Cells. [Internet] [Doctoral dissertation]. University of Houston; 2015. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10657/2018.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-8465-3791. Defining Anti-Tumorigenic and Anti-Inflammatory Effects Mediated By Estrogen Receptor Beta In Colon Epithelial Cells. [Doctoral Dissertation]. University of Houston; 2015. Available from: http://hdl.handle.net/10657/2018

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Houston

21. Butler, Ryan 1986-. Physiological and pathological aspects of the ligand-activated transcription factors: AhR and ERβ.

Degree: PhD, Biology, 2013, University of Houston

 Ligand-activated transcription factors are a diverse group of proteins that are involved a variety of physiological processes. The purpose of these studies was to investigate… (more)

Subjects/Keywords: Aryl hydrocarbon receptor; Estrogen receptors; Transcription factors

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APA (6th Edition):

Butler, R. 1. (2013). Physiological and pathological aspects of the ligand-activated transcription factors: AhR and ERβ. (Doctoral Dissertation). University of Houston. Retrieved from http://hdl.handle.net/10657/956

Chicago Manual of Style (16th Edition):

Butler, Ryan 1986-. “Physiological and pathological aspects of the ligand-activated transcription factors: AhR and ERβ.” 2013. Doctoral Dissertation, University of Houston. Accessed November 27, 2020. http://hdl.handle.net/10657/956.

MLA Handbook (7th Edition):

Butler, Ryan 1986-. “Physiological and pathological aspects of the ligand-activated transcription factors: AhR and ERβ.” 2013. Web. 27 Nov 2020.

Vancouver:

Butler R1. Physiological and pathological aspects of the ligand-activated transcription factors: AhR and ERβ. [Internet] [Doctoral dissertation]. University of Houston; 2013. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10657/956.

Council of Science Editors:

Butler R1. Physiological and pathological aspects of the ligand-activated transcription factors: AhR and ERβ. [Doctoral Dissertation]. University of Houston; 2013. Available from: http://hdl.handle.net/10657/956


University of Canterbury

22. Graham, Lisa Anne. Environmental Estrogens: Assessing Human Gestational Exposure and Interactions with the Estrogen Receptor.

Degree: PhD, Chemistry, 2012, University of Canterbury

 Environmental xenoestrogens (EEs) are chemicals that when they enter the body, the body responds to them as it would to endogenous estrogens. Humans are exposed… (more)

Subjects/Keywords: Estradiol; human effects; gestational exposure; estrogen receptor

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APA (6th Edition):

Graham, L. A. (2012). Environmental Estrogens: Assessing Human Gestational Exposure and Interactions with the Estrogen Receptor. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/8979

Chicago Manual of Style (16th Edition):

Graham, Lisa Anne. “Environmental Estrogens: Assessing Human Gestational Exposure and Interactions with the Estrogen Receptor.” 2012. Doctoral Dissertation, University of Canterbury. Accessed November 27, 2020. http://dx.doi.org/10.26021/8979.

MLA Handbook (7th Edition):

Graham, Lisa Anne. “Environmental Estrogens: Assessing Human Gestational Exposure and Interactions with the Estrogen Receptor.” 2012. Web. 27 Nov 2020.

Vancouver:

Graham LA. Environmental Estrogens: Assessing Human Gestational Exposure and Interactions with the Estrogen Receptor. [Internet] [Doctoral dissertation]. University of Canterbury; 2012. [cited 2020 Nov 27]. Available from: http://dx.doi.org/10.26021/8979.

Council of Science Editors:

Graham LA. Environmental Estrogens: Assessing Human Gestational Exposure and Interactions with the Estrogen Receptor. [Doctoral Dissertation]. University of Canterbury; 2012. Available from: http://dx.doi.org/10.26021/8979


Virginia Tech

23. Rajalekshmi Devi, Sarika. Development of Novel anti-estrogens for endocrine resistant Breast Cancer.

Degree: MS, Chemistry, 2016, Virginia Tech

 ER+ breast cancer raises a significant diagnostic challenge since resistance invariably develops to the current endocrine therapies. 70% of breast cancers are ER+, which results… (more)

Subjects/Keywords: Chemistry; organic; breast cancer; estrogen receptor; OBHS

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APA (6th Edition):

Rajalekshmi Devi, S. (2016). Development of Novel anti-estrogens for endocrine resistant Breast Cancer. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/81275

Chicago Manual of Style (16th Edition):

Rajalekshmi Devi, Sarika. “Development of Novel anti-estrogens for endocrine resistant Breast Cancer.” 2016. Masters Thesis, Virginia Tech. Accessed November 27, 2020. http://hdl.handle.net/10919/81275.

MLA Handbook (7th Edition):

Rajalekshmi Devi, Sarika. “Development of Novel anti-estrogens for endocrine resistant Breast Cancer.” 2016. Web. 27 Nov 2020.

Vancouver:

Rajalekshmi Devi S. Development of Novel anti-estrogens for endocrine resistant Breast Cancer. [Internet] [Masters thesis]. Virginia Tech; 2016. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10919/81275.

Council of Science Editors:

Rajalekshmi Devi S. Development of Novel anti-estrogens for endocrine resistant Breast Cancer. [Masters Thesis]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/81275

24. Baatarsuren, Batmunkh; Narantsog, Choijookhuu; Naparee, Srisowanna; Uugantsetseg, Byambatsogt; Phyu Synn, Oo; Mohmand Noor, Ali; Yamaguchi, Yuya. Estrogen Accelerates Cell Proliferation through Estrogen Receptor α during Rat Liver Regeneration after Partial Hepatectomy.

Degree: 博士(医学), 2017, University of Miyazaki / 宮崎大学

学位論文の一部を構成しているため、http://hdl.handle.net/10458/5984 に本文を掲載。

Although estrogen is implicated in the regulation of cell growth and differentiation in many organs, the exact mechanism for liver regeneration is not… (more)

Subjects/Keywords: estrogen; estrogen receptor α; liver regeneration; partial hepatectomy; cell proliferation

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APA (6th Edition):

Baatarsuren, Batmunkh; Narantsog, Choijookhuu; Naparee, Srisowanna; Uugantsetseg, Byambatsogt; Phyu Synn, Oo; Mohmand Noor, Ali; Yamaguchi, Y. (2017). Estrogen Accelerates Cell Proliferation through Estrogen Receptor α during Rat Liver Regeneration after Partial Hepatectomy. (Thesis). University of Miyazaki / 宮崎大学. Retrieved from http://hdl.handle.net/10458/5983

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Baatarsuren, Batmunkh; Narantsog, Choijookhuu; Naparee, Srisowanna; Uugantsetseg, Byambatsogt; Phyu Synn, Oo; Mohmand Noor, Ali; Yamaguchi, Yuya. “Estrogen Accelerates Cell Proliferation through Estrogen Receptor α during Rat Liver Regeneration after Partial Hepatectomy.” 2017. Thesis, University of Miyazaki / 宮崎大学. Accessed November 27, 2020. http://hdl.handle.net/10458/5983.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Baatarsuren, Batmunkh; Narantsog, Choijookhuu; Naparee, Srisowanna; Uugantsetseg, Byambatsogt; Phyu Synn, Oo; Mohmand Noor, Ali; Yamaguchi, Yuya. “Estrogen Accelerates Cell Proliferation through Estrogen Receptor α during Rat Liver Regeneration after Partial Hepatectomy.” 2017. Web. 27 Nov 2020.

Vancouver:

Baatarsuren, Batmunkh; Narantsog, Choijookhuu; Naparee, Srisowanna; Uugantsetseg, Byambatsogt; Phyu Synn, Oo; Mohmand Noor, Ali; Yamaguchi Y. Estrogen Accelerates Cell Proliferation through Estrogen Receptor α during Rat Liver Regeneration after Partial Hepatectomy. [Internet] [Thesis]. University of Miyazaki / 宮崎大学; 2017. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/10458/5983.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Baatarsuren, Batmunkh; Narantsog, Choijookhuu; Naparee, Srisowanna; Uugantsetseg, Byambatsogt; Phyu Synn, Oo; Mohmand Noor, Ali; Yamaguchi Y. Estrogen Accelerates Cell Proliferation through Estrogen Receptor α during Rat Liver Regeneration after Partial Hepatectomy. [Thesis]. University of Miyazaki / 宮崎大学; 2017. Available from: http://hdl.handle.net/10458/5983

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


UCLA

25. Iorga, Andrea. Estrogen Therapy Rescues Advanced Heart Failure via Estrogen Receptor Beta.

Degree: Molec, Cell, & Integ Physiology, 2015, UCLA

 Cardiac hypertrophy, defined as an enlargement of the ventricles, is often triggered when the heart is subjected to hemodynamic stress from physiological stimuli such as… (more)

Subjects/Keywords: Physiology; Angiogenesis; Aromatase; Estrogen; Estrogen Receptor Beta; Fibrosis; Heart Failure

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APA (6th Edition):

Iorga, A. (2015). Estrogen Therapy Rescues Advanced Heart Failure via Estrogen Receptor Beta. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9f1833b6

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Iorga, Andrea. “Estrogen Therapy Rescues Advanced Heart Failure via Estrogen Receptor Beta.” 2015. Thesis, UCLA. Accessed November 27, 2020. http://www.escholarship.org/uc/item/9f1833b6.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Iorga, Andrea. “Estrogen Therapy Rescues Advanced Heart Failure via Estrogen Receptor Beta.” 2015. Web. 27 Nov 2020.

Vancouver:

Iorga A. Estrogen Therapy Rescues Advanced Heart Failure via Estrogen Receptor Beta. [Internet] [Thesis]. UCLA; 2015. [cited 2020 Nov 27]. Available from: http://www.escholarship.org/uc/item/9f1833b6.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Iorga A. Estrogen Therapy Rescues Advanced Heart Failure via Estrogen Receptor Beta. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/9f1833b6

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Loyola University Chicago

26. Shults, Cody Lee. Mechanisms of Estrogen Receptor Alternative Splicing and the Consequences for Aging in the Female Brain.

Degree: PhD, Cell Biology, Neurobiology and Anatomy, 2015, Loyola University Chicago

  The advances in healthcare and scientific knowledge have resulted in longer life expectancies in women. These advanced ages in women now means that they… (more)

Subjects/Keywords: aging; alternative splicing; estrogen; estrogen receptor; menopause; Endocrinology

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APA (6th Edition):

Shults, C. L. (2015). Mechanisms of Estrogen Receptor Alternative Splicing and the Consequences for Aging in the Female Brain. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/1969

Chicago Manual of Style (16th Edition):

Shults, Cody Lee. “Mechanisms of Estrogen Receptor Alternative Splicing and the Consequences for Aging in the Female Brain.” 2015. Doctoral Dissertation, Loyola University Chicago. Accessed November 27, 2020. https://ecommons.luc.edu/luc_diss/1969.

MLA Handbook (7th Edition):

Shults, Cody Lee. “Mechanisms of Estrogen Receptor Alternative Splicing and the Consequences for Aging in the Female Brain.” 2015. Web. 27 Nov 2020.

Vancouver:

Shults CL. Mechanisms of Estrogen Receptor Alternative Splicing and the Consequences for Aging in the Female Brain. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2015. [cited 2020 Nov 27]. Available from: https://ecommons.luc.edu/luc_diss/1969.

Council of Science Editors:

Shults CL. Mechanisms of Estrogen Receptor Alternative Splicing and the Consequences for Aging in the Female Brain. [Doctoral Dissertation]. Loyola University Chicago; 2015. Available from: https://ecommons.luc.edu/luc_diss/1969


Loyola University Chicago

27. Navarro Negredo, Flor Cecilia. Characterization of the Effects of Sex and Estrogen Receptor Signaling on Antigen-Specific T Cells for Immunotherapy.

Degree: PhD, Biological Science, 2019, Loyola University Chicago

 Adoptive cell transfer (ACT) immunotherapy using antigen (Ag)-specific T cells is partially effective treating several malignancies but numerous challenges remain in order to improve its… (more)

Subjects/Keywords: Estrogen; Estrogen Receptor; Hepatocellular Carcinoma; Immunotherapy; T cells; Tumor Immunology; Biochemistry

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APA (6th Edition):

Navarro Negredo, F. C. (2019). Characterization of the Effects of Sex and Estrogen Receptor Signaling on Antigen-Specific T Cells for Immunotherapy. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/3359

Chicago Manual of Style (16th Edition):

Navarro Negredo, Flor Cecilia. “Characterization of the Effects of Sex and Estrogen Receptor Signaling on Antigen-Specific T Cells for Immunotherapy.” 2019. Doctoral Dissertation, Loyola University Chicago. Accessed November 27, 2020. https://ecommons.luc.edu/luc_diss/3359.

MLA Handbook (7th Edition):

Navarro Negredo, Flor Cecilia. “Characterization of the Effects of Sex and Estrogen Receptor Signaling on Antigen-Specific T Cells for Immunotherapy.” 2019. Web. 27 Nov 2020.

Vancouver:

Navarro Negredo FC. Characterization of the Effects of Sex and Estrogen Receptor Signaling on Antigen-Specific T Cells for Immunotherapy. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2019. [cited 2020 Nov 27]. Available from: https://ecommons.luc.edu/luc_diss/3359.

Council of Science Editors:

Navarro Negredo FC. Characterization of the Effects of Sex and Estrogen Receptor Signaling on Antigen-Specific T Cells for Immunotherapy. [Doctoral Dissertation]. Loyola University Chicago; 2019. Available from: https://ecommons.luc.edu/luc_diss/3359


Texas A&M University

28. Weige, Charles. Estrogen Receptor Beta and p53 Play Integral Roles in Estradiol Mediated Protection against Colon Tumor Development.

Degree: PhD, Genetics, 2012, Texas A&M University

 Hormone replacement therapy and estrogen replacement therapy have shown the ability to reduce risk of colon cancer development in clinical and animal studies, but in… (more)

Subjects/Keywords: Estrogen; estrogen receptor beta; colon cancer; p53; apoptosis; aberrant crypt foci

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APA (6th Edition):

Weige, C. (2012). Estrogen Receptor Beta and p53 Play Integral Roles in Estradiol Mediated Protection against Colon Tumor Development. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11838

Chicago Manual of Style (16th Edition):

Weige, Charles. “Estrogen Receptor Beta and p53 Play Integral Roles in Estradiol Mediated Protection against Colon Tumor Development.” 2012. Doctoral Dissertation, Texas A&M University. Accessed November 27, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11838.

MLA Handbook (7th Edition):

Weige, Charles. “Estrogen Receptor Beta and p53 Play Integral Roles in Estradiol Mediated Protection against Colon Tumor Development.” 2012. Web. 27 Nov 2020.

Vancouver:

Weige C. Estrogen Receptor Beta and p53 Play Integral Roles in Estradiol Mediated Protection against Colon Tumor Development. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11838.

Council of Science Editors:

Weige C. Estrogen Receptor Beta and p53 Play Integral Roles in Estradiol Mediated Protection against Colon Tumor Development. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11838

29. Gustafsson, Karin. Estrogen receptor α and Bone – Posttranslational modifications and cell-specific deletion.

Degree: 2019, University of Gothenburg / Göteborgs Universitet

Estrogen is involved in the regulation and development of reproductive organs. In addition, estrogen regulates several other organs including the skeleton, immune system, and adipose… (more)

Subjects/Keywords: estrogen receptor α; bone; osteoporosis; adipose tissue; estrogen; posttranslational modifications

Page 1 Page 2

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APA (6th Edition):

Gustafsson, K. (2019). Estrogen receptor α and Bone – Posttranslational modifications and cell-specific deletion. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/60795

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gustafsson, Karin. “Estrogen receptor α and Bone – Posttranslational modifications and cell-specific deletion.” 2019. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed November 27, 2020. http://hdl.handle.net/2077/60795.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gustafsson, Karin. “Estrogen receptor α and Bone – Posttranslational modifications and cell-specific deletion.” 2019. Web. 27 Nov 2020.

Vancouver:

Gustafsson K. Estrogen receptor α and Bone – Posttranslational modifications and cell-specific deletion. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2019. [cited 2020 Nov 27]. Available from: http://hdl.handle.net/2077/60795.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gustafsson K. Estrogen receptor α and Bone – Posttranslational modifications and cell-specific deletion. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2019. Available from: http://hdl.handle.net/2077/60795

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Urbana-Champaign

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

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 November 27, 2020. 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. 27 Nov 2020.

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 2020 Nov 27]. 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

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