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You searched for subject:(Androgen receptor). Showing records 1 – 30 of 251 total matches.

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Vanderbilt University

1. Austin, David C. The Role of Nuclear Factor Kappa B in Benign Prostatic Hyperplasia.

Degree: PhD, Cancer Biology, 2016, Vanderbilt University

 Benign prostatic hyperplasia (BPH) is a common, progressive chronic disease. Inflammation is associated with prostatic enlargement and resistance to 5?-reductase inhibitor (5ARI) therapy. Activation of… (more)

Subjects/Keywords: Androgen Receptor Variant 7; Inflammation; Androgen Receptor

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APA (6th Edition):

Austin, D. C. (2016). The Role of Nuclear Factor Kappa B in Benign Prostatic Hyperplasia. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10843

Chicago Manual of Style (16th Edition):

Austin, David C. “The Role of Nuclear Factor Kappa B in Benign Prostatic Hyperplasia.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed May 09, 2021. http://hdl.handle.net/1803/10843.

MLA Handbook (7th Edition):

Austin, David C. “The Role of Nuclear Factor Kappa B in Benign Prostatic Hyperplasia.” 2016. Web. 09 May 2021.

Vancouver:

Austin DC. The Role of Nuclear Factor Kappa B in Benign Prostatic Hyperplasia. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1803/10843.

Council of Science Editors:

Austin DC. The Role of Nuclear Factor Kappa B in Benign Prostatic Hyperplasia. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/10843


University of Illinois – Urbana-Champaign

2. 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 May 09, 2021. 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. 09 May 2021.

Vancouver:

Parent AA. Second-site inhibitors of the estrogen and androgen hormone receptors. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2021 May 09]. 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

3. Takeda, Keisuke. Corepressive function of nuclear receptor coactivator 2 in androgen receptor of prostate cancer cells treated with antiandrogen : 前立腺癌細胞アンドロゲン受容体に対する抗アンドロゲン剤使用時のNCOA2の抑制共役因子作用.

Degree: 博士(医学), 2016, Niigata University / 新潟大学

学位の種類: 博士(医学). 報告番号: 甲第4206号. 学位記番号: 新大院博(医)甲第705号. 学位授与年月日: 平成28年9月20日

BMC Cancer(2016) 16:332

Background: Recruitment of cofactors in the Interaction of the androgen receptor (AR) and AR… (more)

Subjects/Keywords: Androgen receptor; Antiandrogen; Coactivator; Corepressor

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APA (6th Edition):

Takeda, K. (2016). Corepressive function of nuclear receptor coactivator 2 in androgen receptor of prostate cancer cells treated with antiandrogen : 前立腺癌細胞アンドロゲン受容体に対する抗アンドロゲン剤使用時のNCOA2の抑制共役因子作用. (Thesis). Niigata University / 新潟大学. Retrieved from http://hdl.handle.net/10191/45092

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):

Takeda, Keisuke. “Corepressive function of nuclear receptor coactivator 2 in androgen receptor of prostate cancer cells treated with antiandrogen : 前立腺癌細胞アンドロゲン受容体に対する抗アンドロゲン剤使用時のNCOA2の抑制共役因子作用.” 2016. Thesis, Niigata University / 新潟大学. Accessed May 09, 2021. http://hdl.handle.net/10191/45092.

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

MLA Handbook (7th Edition):

Takeda, Keisuke. “Corepressive function of nuclear receptor coactivator 2 in androgen receptor of prostate cancer cells treated with antiandrogen : 前立腺癌細胞アンドロゲン受容体に対する抗アンドロゲン剤使用時のNCOA2の抑制共役因子作用.” 2016. Web. 09 May 2021.

Vancouver:

Takeda K. Corepressive function of nuclear receptor coactivator 2 in androgen receptor of prostate cancer cells treated with antiandrogen : 前立腺癌細胞アンドロゲン受容体に対する抗アンドロゲン剤使用時のNCOA2の抑制共役因子作用. [Internet] [Thesis]. Niigata University / 新潟大学; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/10191/45092.

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

Council of Science Editors:

Takeda K. Corepressive function of nuclear receptor coactivator 2 in androgen receptor of prostate cancer cells treated with antiandrogen : 前立腺癌細胞アンドロゲン受容体に対する抗アンドロゲン剤使用時のNCOA2の抑制共役因子作用. [Thesis]. Niigata University / 新潟大学; 2016. Available from: http://hdl.handle.net/10191/45092

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


University of Minnesota

4. Mutha, Sarita Kumari. Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants.

Degree: 2012, University of Minnesota

University of Minnesota M.S. thesis. Major: Molecular, Cellular, Developmental Biology and Genetics. Advisors. Scott Dehm and Jim McCarthy. 1 computer file (PDF); viii, 45 pages.… (more)

Subjects/Keywords: Androgen receptor; Prostate cancer; Transcription

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APA (6th Edition):

Mutha, S. K. (2012). Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/143853

Chicago Manual of Style (16th Edition):

Mutha, Sarita Kumari. “Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants.” 2012. Masters Thesis, University of Minnesota. Accessed May 09, 2021. http://purl.umn.edu/143853.

MLA Handbook (7th Edition):

Mutha, Sarita Kumari. “Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants.” 2012. Web. 09 May 2021.

Vancouver:

Mutha SK. Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants. [Internet] [Masters thesis]. University of Minnesota; 2012. [cited 2021 May 09]. Available from: http://purl.umn.edu/143853.

Council of Science Editors:

Mutha SK. Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants. [Masters Thesis]. University of Minnesota; 2012. Available from: http://purl.umn.edu/143853


University of Adelaide

5. Trotta, Andrew Paul. Characterisation of the co-chaperone small glutamine-rich tetratricopeptide repeat containing protein alpha as a regulator of androgen receptor activity in prostate cancer cells.

Degree: 2011, University of Adelaide

 Prostate cancer remains one of the leading causes of cancer related morbidity and mortality in Australian men. The androgen receptor (AR) is an intracellular transcription… (more)

Subjects/Keywords: androgen receptor; prostate cancer

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APA (6th Edition):

Trotta, A. P. (2011). Characterisation of the co-chaperone small glutamine-rich tetratricopeptide repeat containing protein alpha as a regulator of androgen receptor activity in prostate cancer cells. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/73205

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):

Trotta, Andrew Paul. “Characterisation of the co-chaperone small glutamine-rich tetratricopeptide repeat containing protein alpha as a regulator of androgen receptor activity in prostate cancer cells.” 2011. Thesis, University of Adelaide. Accessed May 09, 2021. http://hdl.handle.net/2440/73205.

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

MLA Handbook (7th Edition):

Trotta, Andrew Paul. “Characterisation of the co-chaperone small glutamine-rich tetratricopeptide repeat containing protein alpha as a regulator of androgen receptor activity in prostate cancer cells.” 2011. Web. 09 May 2021.

Vancouver:

Trotta AP. Characterisation of the co-chaperone small glutamine-rich tetratricopeptide repeat containing protein alpha as a regulator of androgen receptor activity in prostate cancer cells. [Internet] [Thesis]. University of Adelaide; 2011. [cited 2021 May 09]. Available from: http://hdl.handle.net/2440/73205.

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

Council of Science Editors:

Trotta AP. Characterisation of the co-chaperone small glutamine-rich tetratricopeptide repeat containing protein alpha as a regulator of androgen receptor activity in prostate cancer cells. [Thesis]. University of Adelaide; 2011. Available from: http://hdl.handle.net/2440/73205

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


University of Adelaide

6. Butler, Miriam Simone. The role of small glutamine-rich tetratricopeptide repeat containing protein alpha in female reproductive tissues.

Degree: 2012, University of Adelaide

 Small glutamine-rich tetratricopeptide repeat containing protein alpha (SGTA) is an evolutionarily conserved protein that functions as a mediator of intracellular protein transport. In particular, SGTA… (more)

Subjects/Keywords: SGTA; androgen receptor; ovary

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APA (6th Edition):

Butler, M. S. (2012). The role of small glutamine-rich tetratricopeptide repeat containing protein alpha in female reproductive tissues. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/80189

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):

Butler, Miriam Simone. “The role of small glutamine-rich tetratricopeptide repeat containing protein alpha in female reproductive tissues.” 2012. Thesis, University of Adelaide. Accessed May 09, 2021. http://hdl.handle.net/2440/80189.

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

MLA Handbook (7th Edition):

Butler, Miriam Simone. “The role of small glutamine-rich tetratricopeptide repeat containing protein alpha in female reproductive tissues.” 2012. Web. 09 May 2021.

Vancouver:

Butler MS. The role of small glutamine-rich tetratricopeptide repeat containing protein alpha in female reproductive tissues. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2021 May 09]. Available from: http://hdl.handle.net/2440/80189.

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

Council of Science Editors:

Butler MS. The role of small glutamine-rich tetratricopeptide repeat containing protein alpha in female reproductive tissues. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/80189

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


University of Gothenburg / Göteborgs Universitet

7. Wu, Jianyao. Androgen receptor signaling mechanisms in bone.

Degree: 2018, University of Gothenburg / Göteborgs Universitet

 Osteoporosis is a common age-related disease that increases the risk of fractures. Androgens are crucial for bone health in males. Although a substantial part of… (more)

Subjects/Keywords: androgen receptor; bone; osteoporosis; mouse

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APA (6th Edition):

Wu, J. (2018). Androgen receptor signaling mechanisms in bone. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/57826

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):

Wu, Jianyao. “Androgen receptor signaling mechanisms in bone.” 2018. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed May 09, 2021. http://hdl.handle.net/2077/57826.

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

MLA Handbook (7th Edition):

Wu, Jianyao. “Androgen receptor signaling mechanisms in bone.” 2018. Web. 09 May 2021.

Vancouver:

Wu J. Androgen receptor signaling mechanisms in bone. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2018. [cited 2021 May 09]. Available from: http://hdl.handle.net/2077/57826.

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

Council of Science Editors:

Wu J. Androgen receptor signaling mechanisms in bone. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2018. Available from: http://hdl.handle.net/2077/57826

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


University of Minnesota

8. Mutha, Sarita Kumari. Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants.

Degree: MS, Molecular, Cellular, Developmental Biology and Genetics, 2012, University of Minnesota

 The standard treatment for advanced prostate cancer is chemical castration, which inhibits the activity of the androgen receptor (AR). Eventually, prostate cancer reemerges with a… (more)

Subjects/Keywords: Androgen receptor; Prostate cancer; Transcription

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

APA (6th Edition):

Mutha, S. K. (2012). Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/143853

Chicago Manual of Style (16th Edition):

Mutha, Sarita Kumari. “Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants.” 2012. Masters Thesis, University of Minnesota. Accessed May 09, 2021. http://purl.umn.edu/143853.

MLA Handbook (7th Edition):

Mutha, Sarita Kumari. “Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants.” 2012. Web. 09 May 2021.

Vancouver:

Mutha SK. Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants. [Internet] [Masters thesis]. University of Minnesota; 2012. [cited 2021 May 09]. Available from: http://purl.umn.edu/143853.

Council of Science Editors:

Mutha SK. Role of transcriptional activation unit 5 (TAU5) in mediating transcriptional activity of androgen receptor splice variants. [Masters Thesis]. University of Minnesota; 2012. Available from: http://purl.umn.edu/143853


University of Lund

9. Nenonen, Hannah. Functional characterisation of the CAG polymorphism in the androgen receptor- in vitro and in vivo.

Degree: 2011, University of Lund

 The androgen receptor (AR) is the mediator of androgen actions. In the AR coding region there is a polymorphic CAG repeat encoding a stretch of… (more)

Subjects/Keywords: Clinical Medicine; androgen receptor; polymorphism; CAG polymorphism; androgen receptor activity; infertility; prostate cancer; androgen receptor function

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APA (6th Edition):

Nenonen, H. (2011). Functional characterisation of the CAG polymorphism in the androgen receptor- in vitro and in vivo. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/1845310 ; https://portal.research.lu.se/ws/files/3390473/1845334.pdf

Chicago Manual of Style (16th Edition):

Nenonen, Hannah. “Functional characterisation of the CAG polymorphism in the androgen receptor- in vitro and in vivo.” 2011. Doctoral Dissertation, University of Lund. Accessed May 09, 2021. https://lup.lub.lu.se/record/1845310 ; https://portal.research.lu.se/ws/files/3390473/1845334.pdf.

MLA Handbook (7th Edition):

Nenonen, Hannah. “Functional characterisation of the CAG polymorphism in the androgen receptor- in vitro and in vivo.” 2011. Web. 09 May 2021.

Vancouver:

Nenonen H. Functional characterisation of the CAG polymorphism in the androgen receptor- in vitro and in vivo. [Internet] [Doctoral dissertation]. University of Lund; 2011. [cited 2021 May 09]. Available from: https://lup.lub.lu.se/record/1845310 ; https://portal.research.lu.se/ws/files/3390473/1845334.pdf.

Council of Science Editors:

Nenonen H. Functional characterisation of the CAG polymorphism in the androgen receptor- in vitro and in vivo. [Doctoral Dissertation]. University of Lund; 2011. Available from: https://lup.lub.lu.se/record/1845310 ; https://portal.research.lu.se/ws/files/3390473/1845334.pdf

10. Palethorpe, Helen Marie. Fibroblasts, Androgen Signalling And Oesophageal Adenocarcinoma.

Degree: 2017, University of Adelaide

 Fibroblasts and androgen signalling can influence the biology of cancer. In this thesis their role has been explored in oesophageal adenocarcinoma (OAC), and in prostate… (more)

Subjects/Keywords: Androgen receptor; androgen signalling; dihydrotestosterone; fibroblasts; myofibroblasts; oesophageal adenocarcinoma; prostate cancer

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APA (6th Edition):

Palethorpe, H. M. (2017). Fibroblasts, Androgen Signalling And Oesophageal Adenocarcinoma. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/122069

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):

Palethorpe, Helen Marie. “Fibroblasts, Androgen Signalling And Oesophageal Adenocarcinoma.” 2017. Thesis, University of Adelaide. Accessed May 09, 2021. http://hdl.handle.net/2440/122069.

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

MLA Handbook (7th Edition):

Palethorpe, Helen Marie. “Fibroblasts, Androgen Signalling And Oesophageal Adenocarcinoma.” 2017. Web. 09 May 2021.

Vancouver:

Palethorpe HM. Fibroblasts, Androgen Signalling And Oesophageal Adenocarcinoma. [Internet] [Thesis]. University of Adelaide; 2017. [cited 2021 May 09]. Available from: http://hdl.handle.net/2440/122069.

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

Council of Science Editors:

Palethorpe HM. Fibroblasts, Androgen Signalling And Oesophageal Adenocarcinoma. [Thesis]. University of Adelaide; 2017. Available from: http://hdl.handle.net/2440/122069

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


University of Minnesota

11. Brand, Lucas. Therapeutic Targeting of Intrinsically Disordered Androgen Recptor Functional Domains in Prostate Cancer.

Degree: PhD, Microbiology, Immunology and Cancer Biology, 2015, University of Minnesota

 Prostate cancer (PCa) is a leading cause of morbidity and mortality in the United States, and contributes to a significant healthcare burden due to an… (more)

Subjects/Keywords: Alkylating Agent; Androgen Deprivation Therapy; Androgen Receptor; Intrinsic Disorder; Prostate Cancer

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APA (6th Edition):

Brand, L. (2015). Therapeutic Targeting of Intrinsically Disordered Androgen Recptor Functional Domains in Prostate Cancer. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/174842

Chicago Manual of Style (16th Edition):

Brand, Lucas. “Therapeutic Targeting of Intrinsically Disordered Androgen Recptor Functional Domains in Prostate Cancer.” 2015. Doctoral Dissertation, University of Minnesota. Accessed May 09, 2021. http://hdl.handle.net/11299/174842.

MLA Handbook (7th Edition):

Brand, Lucas. “Therapeutic Targeting of Intrinsically Disordered Androgen Recptor Functional Domains in Prostate Cancer.” 2015. Web. 09 May 2021.

Vancouver:

Brand L. Therapeutic Targeting of Intrinsically Disordered Androgen Recptor Functional Domains in Prostate Cancer. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/11299/174842.

Council of Science Editors:

Brand L. Therapeutic Targeting of Intrinsically Disordered Androgen Recptor Functional Domains in Prostate Cancer. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/174842


University of Texas – Austin

12. Zhang, Chenan. Testosterone acts at the cell surface to induce granulosa/theca cell death via an apoptotic pathway in Atlantic croaker (Micropogonias undulatus).

Degree: MSin Marine Science, Marine Science, 2011, University of Texas – Austin

 The teleost ovarian follicle undergoes extensive remodeling and regression during the reproductive cycle—a process involving apoptosis and cell death. However, the hormonal regulation of these… (more)

Subjects/Keywords: Androgen; Apoptosis; Cell death; Membrane androgen receptor; Ovary; Teleost; Testosterone; Bax

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APA (6th Edition):

Zhang, C. (2011). Testosterone acts at the cell surface to induce granulosa/theca cell death via an apoptotic pathway in Atlantic croaker (Micropogonias undulatus). (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/23902

Chicago Manual of Style (16th Edition):

Zhang, Chenan. “Testosterone acts at the cell surface to induce granulosa/theca cell death via an apoptotic pathway in Atlantic croaker (Micropogonias undulatus).” 2011. Masters Thesis, University of Texas – Austin. Accessed May 09, 2021. http://hdl.handle.net/2152/23902.

MLA Handbook (7th Edition):

Zhang, Chenan. “Testosterone acts at the cell surface to induce granulosa/theca cell death via an apoptotic pathway in Atlantic croaker (Micropogonias undulatus).” 2011. Web. 09 May 2021.

Vancouver:

Zhang C. Testosterone acts at the cell surface to induce granulosa/theca cell death via an apoptotic pathway in Atlantic croaker (Micropogonias undulatus). [Internet] [Masters thesis]. University of Texas – Austin; 2011. [cited 2021 May 09]. Available from: http://hdl.handle.net/2152/23902.

Council of Science Editors:

Zhang C. Testosterone acts at the cell surface to induce granulosa/theca cell death via an apoptotic pathway in Atlantic croaker (Micropogonias undulatus). [Masters Thesis]. University of Texas – Austin; 2011. Available from: http://hdl.handle.net/2152/23902


University of Rochester

13. Hsu, Jong-Wei. Androgen Receptor and Vitamin D Signaling in Bladder Cancer.

Degree: PhD, 2012, University of Rochester

 Bladder cancer (BCa) is the fourth most common cancer in American men, and was estimated to be diagnosed in 70,530 people and cause 14,680 deaths… (more)

Subjects/Keywords: Bladder Cancer; Vitamin D; Androgen Receptor

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APA (6th Edition):

Hsu, J. (2012). Androgen Receptor and Vitamin D Signaling in Bladder Cancer. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/19819

Chicago Manual of Style (16th Edition):

Hsu, Jong-Wei. “Androgen Receptor and Vitamin D Signaling in Bladder Cancer.” 2012. Doctoral Dissertation, University of Rochester. Accessed May 09, 2021. http://hdl.handle.net/1802/19819.

MLA Handbook (7th Edition):

Hsu, Jong-Wei. “Androgen Receptor and Vitamin D Signaling in Bladder Cancer.” 2012. Web. 09 May 2021.

Vancouver:

Hsu J. Androgen Receptor and Vitamin D Signaling in Bladder Cancer. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2021 May 09]. Available from: http://hdl.handle.net/1802/19819.

Council of Science Editors:

Hsu J. Androgen Receptor and Vitamin D Signaling in Bladder Cancer. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/19819


University of Toronto

14. Ramzan, Firyal M. Effects of Androgen Receptor Overexpression on Select Sexually Dimorphic Neural Structures.

Degree: 2014, University of Toronto

There are a number of interesting sexual dimorphisms studied in the brain, each of which is affected by hormones in different ways. The purpose of… (more)

Subjects/Keywords: androgen receptor; differentiation; sex difference; transgenic; 0317

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APA (6th Edition):

Ramzan, F. M. (2014). Effects of Androgen Receptor Overexpression on Select Sexually Dimorphic Neural Structures. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70450

Chicago Manual of Style (16th Edition):

Ramzan, Firyal M. “Effects of Androgen Receptor Overexpression on Select Sexually Dimorphic Neural Structures.” 2014. Masters Thesis, University of Toronto. Accessed May 09, 2021. http://hdl.handle.net/1807/70450.

MLA Handbook (7th Edition):

Ramzan, Firyal M. “Effects of Androgen Receptor Overexpression on Select Sexually Dimorphic Neural Structures.” 2014. Web. 09 May 2021.

Vancouver:

Ramzan FM. Effects of Androgen Receptor Overexpression on Select Sexually Dimorphic Neural Structures. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/1807/70450.

Council of Science Editors:

Ramzan FM. Effects of Androgen Receptor Overexpression on Select Sexually Dimorphic Neural Structures. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/70450

15. Faber, P.W. Characterization of the androgen receptor transcription unit.

Degree: 1993, Erasmus University Medical Center

 textabstractln this study the androgen receptor (AR) transcription unit is presented. Chapter II describes the isolation and characterization of one genomic clone, from which the… (more)

Subjects/Keywords: DNA; androgen receptor

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APA (6th Edition):

Faber, P. W. (1993). Characterization of the androgen receptor transcription unit. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/39449

Chicago Manual of Style (16th Edition):

Faber, P W. “Characterization of the androgen receptor transcription unit.” 1993. Doctoral Dissertation, Erasmus University Medical Center. Accessed May 09, 2021. http://hdl.handle.net/1765/39449.

MLA Handbook (7th Edition):

Faber, P W. “Characterization of the androgen receptor transcription unit.” 1993. Web. 09 May 2021.

Vancouver:

Faber PW. Characterization of the androgen receptor transcription unit. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 1993. [cited 2021 May 09]. Available from: http://hdl.handle.net/1765/39449.

Council of Science Editors:

Faber PW. Characterization of the androgen receptor transcription unit. [Doctoral Dissertation]. Erasmus University Medical Center; 1993. Available from: http://hdl.handle.net/1765/39449


University of Cambridge

16. Fowler, Elaine. Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor.

Degree: PhD, 2020, University of Cambridge

 Proteolysis targeting chimeras (PROTACs) are an emerging field of therapeutics and promising potential drug candidates. PROTACs consist of a target protein binder connected via a… (more)

Subjects/Keywords: PROTAC; MDM2; Androgen Receptor; Photoswitch; Azobenzene

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APA (6th Edition):

Fowler, E. (2020). Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/305449

Chicago Manual of Style (16th Edition):

Fowler, Elaine. “Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor.” 2020. Doctoral Dissertation, University of Cambridge. Accessed May 09, 2021. https://www.repository.cam.ac.uk/handle/1810/305449.

MLA Handbook (7th Edition):

Fowler, Elaine. “Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor.” 2020. Web. 09 May 2021.

Vancouver:

Fowler E. Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 May 09]. Available from: https://www.repository.cam.ac.uk/handle/1810/305449.

Council of Science Editors:

Fowler E. Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/305449


University of Cambridge

17. Fowler, Elaine. Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor.

Degree: PhD, 2020, University of Cambridge

 Proteolysis targeting chimeras (PROTACs) are an emerging field of therapeutics and promising potential drug candidates. PROTACs consist of a target protein binder connected via a… (more)

Subjects/Keywords: 572; PROTAC; MDM2; Androgen Receptor; Photoswitch; Azobenzene

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APA (6th Edition):

Fowler, E. (2020). Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.52529 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805947

Chicago Manual of Style (16th Edition):

Fowler, Elaine. “Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor.” 2020. Doctoral Dissertation, University of Cambridge. Accessed May 09, 2021. https://doi.org/10.17863/CAM.52529 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805947.

MLA Handbook (7th Edition):

Fowler, Elaine. “Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor.” 2020. Web. 09 May 2021.

Vancouver:

Fowler E. Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 May 09]. Available from: https://doi.org/10.17863/CAM.52529 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805947.

Council of Science Editors:

Fowler E. Proteolysis targeting chimeras for the directed ubiquitination of the androgen receptor. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://doi.org/10.17863/CAM.52529 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805947


University of Melbourne

18. Pang, Pui Shi. Investigating non-DNA binding-dependent signalling pathways of the androgen receptor.

Degree: 2013, University of Melbourne

 Androgens regulate the development and function of reproductive and non-reproductive tissues, including muscle, bone and fat. Androgens induce their effects by binding to the androgen(more)

Subjects/Keywords: androgen receptor; non-genomic signalling pathway

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

APA (6th Edition):

Pang, P. S. (2013). Investigating non-DNA binding-dependent signalling pathways of the androgen receptor. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38116

Chicago Manual of Style (16th Edition):

Pang, Pui Shi. “Investigating non-DNA binding-dependent signalling pathways of the androgen receptor.” 2013. Doctoral Dissertation, University of Melbourne. Accessed May 09, 2021. http://hdl.handle.net/11343/38116.

MLA Handbook (7th Edition):

Pang, Pui Shi. “Investigating non-DNA binding-dependent signalling pathways of the androgen receptor.” 2013. Web. 09 May 2021.

Vancouver:

Pang PS. Investigating non-DNA binding-dependent signalling pathways of the androgen receptor. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2021 May 09]. Available from: http://hdl.handle.net/11343/38116.

Council of Science Editors:

Pang PS. Investigating non-DNA binding-dependent signalling pathways of the androgen receptor. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38116


Georgia State University

19. Schuppe, Eric. Conserved androgenic differentiation pathways are repurposed during the evolution of adult sexual plasticity.

Degree: MS, Biology, 2014, Georgia State University

  Early exposure to androgens is necessary to organize male phenotype, and inhibition of androgen signaling adversely affects external genitalia development. Nonetheless, vertebrates that remain… (more)

Subjects/Keywords: Androgen receptor; sexual plasticity; sexual differentiation

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APA (6th Edition):

Schuppe, E. (2014). Conserved androgenic differentiation pathways are repurposed during the evolution of adult sexual plasticity. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_theses/61

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):

Schuppe, Eric. “Conserved androgenic differentiation pathways are repurposed during the evolution of adult sexual plasticity.” 2014. Thesis, Georgia State University. Accessed May 09, 2021. https://scholarworks.gsu.edu/biology_theses/61.

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

MLA Handbook (7th Edition):

Schuppe, Eric. “Conserved androgenic differentiation pathways are repurposed during the evolution of adult sexual plasticity.” 2014. Web. 09 May 2021.

Vancouver:

Schuppe E. Conserved androgenic differentiation pathways are repurposed during the evolution of adult sexual plasticity. [Internet] [Thesis]. Georgia State University; 2014. [cited 2021 May 09]. Available from: https://scholarworks.gsu.edu/biology_theses/61.

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

Council of Science Editors:

Schuppe E. Conserved androgenic differentiation pathways are repurposed during the evolution of adult sexual plasticity. [Thesis]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/biology_theses/61

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


University of Iowa

20. Hsiao, Jordy Jame. Quantitative proteomics of androgen receptor-mediated signaling networks in prostate tumor cells.

Degree: PhD, Molecular Physiology and Biophysics, 2015, University of Iowa

  Aberrant androgen receptor (AR) activity plays a critical role in the development and progression of both early-staged organ-confined and late-staged metastatic human prostate cancer.… (more)

Subjects/Keywords: Androgen; Androgen receptor; Mass Spectrometry; Protein complexes; Proteomics; Steroid hormone receptor; Biophysics

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

APA (6th Edition):

Hsiao, J. J. (2015). Quantitative proteomics of androgen receptor-mediated signaling networks in prostate tumor cells. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5506

Chicago Manual of Style (16th Edition):

Hsiao, Jordy Jame. “Quantitative proteomics of androgen receptor-mediated signaling networks in prostate tumor cells.” 2015. Doctoral Dissertation, University of Iowa. Accessed May 09, 2021. https://ir.uiowa.edu/etd/5506.

MLA Handbook (7th Edition):

Hsiao, Jordy Jame. “Quantitative proteomics of androgen receptor-mediated signaling networks in prostate tumor cells.” 2015. Web. 09 May 2021.

Vancouver:

Hsiao JJ. Quantitative proteomics of androgen receptor-mediated signaling networks in prostate tumor cells. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2021 May 09]. Available from: https://ir.uiowa.edu/etd/5506.

Council of Science Editors:

Hsiao JJ. Quantitative proteomics of androgen receptor-mediated signaling networks in prostate tumor cells. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/5506


Monash University

21. KWAN, EDMOND MICHAEL KAM MING. WHOLE BLOOD TRANSCRIPTOMIC ANALYSIS AS BIOMARKERS IN METASTATIC PROSTATE CANCER.

Degree: Medicine, Nursing and Health Sciences, 2020, Monash University

 Treatment options for men with advanced prostate cancer have rapidly improved in the last decade. Despite this, choosing the best treatment for individual patients remains… (more)

Subjects/Keywords: Biomarkers; Cancer Genetics; Androgen receptor; biomarkers; androgen receptor splice variant; advanced prostate cancer; prognosis

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APA (6th Edition):

KWAN, E. M. K. M. (2020). WHOLE BLOOD TRANSCRIPTOMIC ANALYSIS AS BIOMARKERS IN METASTATIC PROSTATE CANCER. (Thesis). Monash University. Retrieved from http://hdl.handle.net/10.26180/5f0bb4645d719

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):

KWAN, EDMOND MICHAEL KAM MING. “WHOLE BLOOD TRANSCRIPTOMIC ANALYSIS AS BIOMARKERS IN METASTATIC PROSTATE CANCER.” 2020. Thesis, Monash University. Accessed May 09, 2021. http://hdl.handle.net/10.26180/5f0bb4645d719.

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

MLA Handbook (7th Edition):

KWAN, EDMOND MICHAEL KAM MING. “WHOLE BLOOD TRANSCRIPTOMIC ANALYSIS AS BIOMARKERS IN METASTATIC PROSTATE CANCER.” 2020. Web. 09 May 2021.

Vancouver:

KWAN EMKM. WHOLE BLOOD TRANSCRIPTOMIC ANALYSIS AS BIOMARKERS IN METASTATIC PROSTATE CANCER. [Internet] [Thesis]. Monash University; 2020. [cited 2021 May 09]. Available from: http://hdl.handle.net/10.26180/5f0bb4645d719.

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

Council of Science Editors:

KWAN EMKM. WHOLE BLOOD TRANSCRIPTOMIC ANALYSIS AS BIOMARKERS IN METASTATIC PROSTATE CANCER. [Thesis]. Monash University; 2020. Available from: http://hdl.handle.net/10.26180/5f0bb4645d719

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


Stellenbosch University

22. Ndlovu, Easter. Crosstalk between the androgen and estrogen receptors in breast cancer.

Degree: MSc, Biochemistry, 2016, Stellenbosch University

 ENGLISH ABSTRACT: Hormone replacement therapy (HRT) is used by post-menopausal women to alleviate symptoms associated with decreased endogenous estrogen levels, such as hot flashes and… (more)

Subjects/Keywords: Breast cancer; Androgen receptor; Estrogen receptor; Hormone replacement therapy; UCTD

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

APA (6th Edition):

Ndlovu, E. (2016). Crosstalk between the androgen and estrogen receptors in breast cancer. (Masters Thesis). Stellenbosch University. Retrieved from http://hdl.handle.net/10019.1/98345

Chicago Manual of Style (16th Edition):

Ndlovu, Easter. “Crosstalk between the androgen and estrogen receptors in breast cancer.” 2016. Masters Thesis, Stellenbosch University. Accessed May 09, 2021. http://hdl.handle.net/10019.1/98345.

MLA Handbook (7th Edition):

Ndlovu, Easter. “Crosstalk between the androgen and estrogen receptors in breast cancer.” 2016. Web. 09 May 2021.

Vancouver:

Ndlovu E. Crosstalk between the androgen and estrogen receptors in breast cancer. [Internet] [Masters thesis]. Stellenbosch University; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/10019.1/98345.

Council of Science Editors:

Ndlovu E. Crosstalk between the androgen and estrogen receptors in breast cancer. [Masters Thesis]. Stellenbosch University; 2016. Available from: http://hdl.handle.net/10019.1/98345


University of Illinois – Chicago

23. Abeer M. Mahmoud (7919072). Androgen Receptor Mutations and Estrogen Receptor-β Modulate Genistein Effects on Prostate Cancer Cells.

Degree: 2013, University of Illinois – Chicago

 Genistein is the most abundant and potent isoflavone in soy and it has an estradiol-like structure. Results from previous studies examining genistein effects on androgen(more)

Subjects/Keywords: Uncategorized; prostate cancer; androgen receptor; estrogen receptor; genistein; soy isoflavones; mutations

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APA (6th Edition):

(7919072), A. M. M. (2013). Androgen Receptor Mutations and Estrogen Receptor-β Modulate Genistein Effects on Prostate Cancer Cells. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10017

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):

(7919072), Abeer M. Mahmoud. “Androgen Receptor Mutations and Estrogen Receptor-β Modulate Genistein Effects on Prostate Cancer Cells.” 2013. Thesis, University of Illinois – Chicago. Accessed May 09, 2021. http://hdl.handle.net/10027/10017.

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

MLA Handbook (7th Edition):

(7919072), Abeer M. Mahmoud. “Androgen Receptor Mutations and Estrogen Receptor-β Modulate Genistein Effects on Prostate Cancer Cells.” 2013. Web. 09 May 2021.

Vancouver:

(7919072) AMM. Androgen Receptor Mutations and Estrogen Receptor-β Modulate Genistein Effects on Prostate Cancer Cells. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2021 May 09]. Available from: http://hdl.handle.net/10027/10017.

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

Council of Science Editors:

(7919072) AMM. Androgen Receptor Mutations and Estrogen Receptor-β Modulate Genistein Effects on Prostate Cancer Cells. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10017

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


University of California – San Diego

24. Ryan, Genevieve Elaine. Neuroendocrine Actions of Androgens in Male and Female Reproduction.

Degree: Biomedical Sciences, 2018, University of California – San Diego

 Androgens and androgen receptor (AR) have important roles in both male and female reproductive physiology. In males, androgens are critical for sexual differentiation, the development… (more)

Subjects/Keywords: Endocrinology; Neurosciences; Molecular biology; androgen excess; androgen receptor; kisspeptin; pituitary gonadotrope; polycystic ovary syndrome

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APA (6th Edition):

Ryan, G. E. (2018). Neuroendocrine Actions of Androgens in Male and Female Reproduction. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/0bm5x61w

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):

Ryan, Genevieve Elaine. “Neuroendocrine Actions of Androgens in Male and Female Reproduction.” 2018. Thesis, University of California – San Diego. Accessed May 09, 2021. http://www.escholarship.org/uc/item/0bm5x61w.

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

MLA Handbook (7th Edition):

Ryan, Genevieve Elaine. “Neuroendocrine Actions of Androgens in Male and Female Reproduction.” 2018. Web. 09 May 2021.

Vancouver:

Ryan GE. Neuroendocrine Actions of Androgens in Male and Female Reproduction. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2021 May 09]. Available from: http://www.escholarship.org/uc/item/0bm5x61w.

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

Council of Science Editors:

Ryan GE. Neuroendocrine Actions of Androgens in Male and Female Reproduction. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/0bm5x61w

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


University of Kentucky

25. Begemann, Diane. Prostate Cancer Resistance to Cabazitaxel Chemotherapy.

Degree: 2020, University of Kentucky

 The plasticity of prostate tumors contributes to the heterogeneity in response and acquisition of therapeutic resistance in advanced prostate cancer. Disruption of the phenotypic landscape… (more)

Subjects/Keywords: Prostate Cancer; Androgen Receptor; Microtubules; Taxanes; Anti-Androgen; Castration Resistant Prostate Cancer; Cancer Biology

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APA (6th Edition):

Begemann, D. (2020). Prostate Cancer Resistance to Cabazitaxel Chemotherapy. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/toxicology_etds/31

Chicago Manual of Style (16th Edition):

Begemann, Diane. “Prostate Cancer Resistance to Cabazitaxel Chemotherapy.” 2020. Doctoral Dissertation, University of Kentucky. Accessed May 09, 2021. https://uknowledge.uky.edu/toxicology_etds/31.

MLA Handbook (7th Edition):

Begemann, Diane. “Prostate Cancer Resistance to Cabazitaxel Chemotherapy.” 2020. Web. 09 May 2021.

Vancouver:

Begemann D. Prostate Cancer Resistance to Cabazitaxel Chemotherapy. [Internet] [Doctoral dissertation]. University of Kentucky; 2020. [cited 2021 May 09]. Available from: https://uknowledge.uky.edu/toxicology_etds/31.

Council of Science Editors:

Begemann D. Prostate Cancer Resistance to Cabazitaxel Chemotherapy. [Doctoral Dissertation]. University of Kentucky; 2020. Available from: https://uknowledge.uky.edu/toxicology_etds/31


University of Southern California

26. Liang, Mengmeng. Homologous cell systems for the study of progression of androgen-dependent prostate cancer to castration-resistant prostate cancer.

Degree: PhD, Pathobiology, 2013, University of Southern California

 Despite immense research progress made in recent years, the recurrence of castration-resistant prostate cancer (CRPC) still remains poorly understood. Androgen receptor (AR), an essential player… (more)

Subjects/Keywords: androgen-dependent and castration-resistant prostate cancer; androgen receptor; androgen receptor splice variants; conditional Pten-deletion mouse model of prostate cancer; mouse prostate cancer cell lines

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

APA (6th Edition):

Liang, M. (2013). Homologous cell systems for the study of progression of androgen-dependent prostate cancer to castration-resistant prostate cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323393/rec/3218

Chicago Manual of Style (16th Edition):

Liang, Mengmeng. “Homologous cell systems for the study of progression of androgen-dependent prostate cancer to castration-resistant prostate cancer.” 2013. Doctoral Dissertation, University of Southern California. Accessed May 09, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323393/rec/3218.

MLA Handbook (7th Edition):

Liang, Mengmeng. “Homologous cell systems for the study of progression of androgen-dependent prostate cancer to castration-resistant prostate cancer.” 2013. Web. 09 May 2021.

Vancouver:

Liang M. Homologous cell systems for the study of progression of androgen-dependent prostate cancer to castration-resistant prostate cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 May 09]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323393/rec/3218.

Council of Science Editors:

Liang M. Homologous cell systems for the study of progression of androgen-dependent prostate cancer to castration-resistant prostate cancer. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/323393/rec/3218


Universidade Estadual de Campinas

27. da Silva, Julio Cesar Araujo, 1974-. Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular.

Degree: Instituto de Química; Programa de Pós-Graduação em Química, 2012, Universidade Estadual de Campinas

Orientador: Munir Salomão Skaf

Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química

Made available in DSpace on 2018-08-21T17:39:27Z (GMT). No. of bitstreams: 1… (more)

Subjects/Keywords: Receptor nuclear; Receptor de androgênio; Simulação de dinâmica molecular; Nuclear receptor; Androgen receptor; Molecular dynamics simulations

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APA (6th Edition):

da Silva, Julio Cesar Araujo, 1. (2012). Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular. (Doctoral Dissertation). Universidade Estadual de Campinas. Retrieved from DA SILVA, Julio Cesar Araujo. Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular. 2012. 94 p. Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/248861>. Acesso em: 21 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/248861

Chicago Manual of Style (16th Edition):

da Silva, Julio Cesar Araujo, 1974-. “Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular.” 2012. Doctoral Dissertation, Universidade Estadual de Campinas. Accessed May 09, 2021. DA SILVA, Julio Cesar Araujo. Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular. 2012. 94 p. Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/248861>. Acesso em: 21 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/248861.

MLA Handbook (7th Edition):

da Silva, Julio Cesar Araujo, 1974-. “Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular.” 2012. Web. 09 May 2021.

Vancouver:

da Silva, Julio Cesar Araujo 1. Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular. [Internet] [Doctoral dissertation]. Universidade Estadual de Campinas; 2012. [cited 2021 May 09]. Available from: DA SILVA, Julio Cesar Araujo. Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular. 2012. 94 p. Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/248861>. Acesso em: 21 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/248861.

Council of Science Editors:

da Silva, Julio Cesar Araujo 1. Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular. [Doctoral Dissertation]. Universidade Estadual de Campinas; 2012. Available from: DA SILVA, Julio Cesar Araujo. Bases moleculares da diminuição da capacidade funcional do receptor de androgênio mutado estudadas por simulações de dinâmica molecular. 2012. 94 p. Tese (doutorado) - Universidade Estadual de Campinas, Instituto de Química, Campinas, SP. Disponível em: <http://www.repositorio.unicamp.br/handle/REPOSIP/248861>. Acesso em: 21 ago. 2018. ; http://repositorio.unicamp.br/jspui/handle/REPOSIP/248861


Universidad del Rosario

28. Rangel Jiménez, Nelson Enrique. "New molecular approches using AR, FOXA1 and HER2 for outcome classification of estrogen Receptor-Positive (ER+) breast cancers”.

Degree: 2018, Universidad del Rosario

Here, we studied new prognostic and predictive easy access strategies in breast cancer (molecular markers), for better classify ER+ breast cancer disease, which might provide… (more)

Subjects/Keywords: Breast cancer; Androgen Receptor; Estrogen Receptor; Prognosis; Molecular medicine; 616; Neoplasias de la mama; Receptores androgénicos; Medicina molecular; Breast cancer; Androgen Receptor; Estrogen Receptor; Prognosis; Molecular medicine

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

APA (6th Edition):

Rangel Jiménez, N. E. (2018). "New molecular approches using AR, FOXA1 and HER2 for outcome classification of estrogen Receptor-Positive (ER+) breast cancers”. (Thesis). Universidad del Rosario. Retrieved from http://repository.urosario.edu.co/handle/10336/18932

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):

Rangel Jiménez, Nelson Enrique. “"New molecular approches using AR, FOXA1 and HER2 for outcome classification of estrogen Receptor-Positive (ER+) breast cancers”.” 2018. Thesis, Universidad del Rosario. Accessed May 09, 2021. http://repository.urosario.edu.co/handle/10336/18932.

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

MLA Handbook (7th Edition):

Rangel Jiménez, Nelson Enrique. “"New molecular approches using AR, FOXA1 and HER2 for outcome classification of estrogen Receptor-Positive (ER+) breast cancers”.” 2018. Web. 09 May 2021.

Vancouver:

Rangel Jiménez NE. "New molecular approches using AR, FOXA1 and HER2 for outcome classification of estrogen Receptor-Positive (ER+) breast cancers”. [Internet] [Thesis]. Universidad del Rosario; 2018. [cited 2021 May 09]. Available from: http://repository.urosario.edu.co/handle/10336/18932.

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

Council of Science Editors:

Rangel Jiménez NE. "New molecular approches using AR, FOXA1 and HER2 for outcome classification of estrogen Receptor-Positive (ER+) breast cancers”. [Thesis]. Universidad del Rosario; 2018. Available from: http://repository.urosario.edu.co/handle/10336/18932

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


Vanderbilt University

29. Fuseini, Hubaida. The Role of Ovarian Hormones and Testosterone on Type 2 and IL-17A-Mediated Airway inflammation.

Degree: PhD, Microbiology and Immunology, 2019, Vanderbilt University

 Severe asthma is a significant health care concern, with patients having poorer asthma control, poorer lung function, and increased health care costs compared to milder… (more)

Subjects/Keywords: type 2; testosterone; ovarian hormones; estrogen receptor alpha; asthma; androgen receptor; IL-17A

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

APA (6th Edition):

Fuseini, H. (2019). The Role of Ovarian Hormones and Testosterone on Type 2 and IL-17A-Mediated Airway inflammation. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11949

Chicago Manual of Style (16th Edition):

Fuseini, Hubaida. “The Role of Ovarian Hormones and Testosterone on Type 2 and IL-17A-Mediated Airway inflammation.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed May 09, 2021. http://hdl.handle.net/1803/11949.

MLA Handbook (7th Edition):

Fuseini, Hubaida. “The Role of Ovarian Hormones and Testosterone on Type 2 and IL-17A-Mediated Airway inflammation.” 2019. Web. 09 May 2021.

Vancouver:

Fuseini H. The Role of Ovarian Hormones and Testosterone on Type 2 and IL-17A-Mediated Airway inflammation. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 May 09]. Available from: http://hdl.handle.net/1803/11949.

Council of Science Editors:

Fuseini H. The Role of Ovarian Hormones and Testosterone on Type 2 and IL-17A-Mediated Airway inflammation. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/11949


University of Melbourne

30. Chen, Yu. Hormone-responsive networks influence urethral closure and phallus growth.

Degree: 2018, University of Melbourne

 Phallus development in mammals is androgen-dependent but can be affected by oestrogen. Many genes that are important in regulating phallus development in mice are also… (more)

Subjects/Keywords: hypospadias; lncRNA; RNA-Seq; WGCNA; marsupial; androstanediol; phallus; androgen receptor; oestrogen receptor; castration

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

APA (6th Edition):

Chen, Y. (2018). Hormone-responsive networks influence urethral closure and phallus growth. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/221906

Chicago Manual of Style (16th Edition):

Chen, Yu. “Hormone-responsive networks influence urethral closure and phallus growth.” 2018. Doctoral Dissertation, University of Melbourne. Accessed May 09, 2021. http://hdl.handle.net/11343/221906.

MLA Handbook (7th Edition):

Chen, Yu. “Hormone-responsive networks influence urethral closure and phallus growth.” 2018. Web. 09 May 2021.

Vancouver:

Chen Y. Hormone-responsive networks influence urethral closure and phallus growth. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2021 May 09]. Available from: http://hdl.handle.net/11343/221906.

Council of Science Editors:

Chen Y. Hormone-responsive networks influence urethral closure and phallus growth. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/221906

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