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You searched for subject:(gpr30). Showing records 1 – 19 of 19 total matches.

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1. Menad, Rafik. Régulation fonctionnelle de l’épididyme d’un rongeur déserticole, Psammomys obesus, CRETZSCHMAR, 1828 : Functional Regulation of Epididymis of Sand Rat Psammomys obesus, CRETZSCHMAR, 1828.

Degree: Docteur es, Sciences biologiques, 2015, Paris, EPHE; Université des sciences et de la technologie Houari Boumediene (Alger)

Afin de mettre en évidence les principaux éléments de la voie androgénique et œstrogénique dans l’épididyme du rat des sables adulte, capturé dans la région… (more)

Subjects/Keywords: P450 aromatase; GPR30; P450 aromatase; GPR30; Epididymis; Apoptosis; Estrogen Receptors; Androgen Receptors

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

APA (6th Edition):

Menad, R. (2015). Régulation fonctionnelle de l’épididyme d’un rongeur déserticole, Psammomys obesus, CRETZSCHMAR, 1828 : Functional Regulation of Epididymis of Sand Rat Psammomys obesus, CRETZSCHMAR, 1828. (Doctoral Dissertation). Paris, EPHE; Université des sciences et de la technologie Houari Boumediene (Alger). Retrieved from http://www.theses.fr/2015EPHE3011

Chicago Manual of Style (16th Edition):

Menad, Rafik. “Régulation fonctionnelle de l’épididyme d’un rongeur déserticole, Psammomys obesus, CRETZSCHMAR, 1828 : Functional Regulation of Epididymis of Sand Rat Psammomys obesus, CRETZSCHMAR, 1828.” 2015. Doctoral Dissertation, Paris, EPHE; Université des sciences et de la technologie Houari Boumediene (Alger). Accessed October 27, 2020. http://www.theses.fr/2015EPHE3011.

MLA Handbook (7th Edition):

Menad, Rafik. “Régulation fonctionnelle de l’épididyme d’un rongeur déserticole, Psammomys obesus, CRETZSCHMAR, 1828 : Functional Regulation of Epididymis of Sand Rat Psammomys obesus, CRETZSCHMAR, 1828.” 2015. Web. 27 Oct 2020.

Vancouver:

Menad R. Régulation fonctionnelle de l’épididyme d’un rongeur déserticole, Psammomys obesus, CRETZSCHMAR, 1828 : Functional Regulation of Epididymis of Sand Rat Psammomys obesus, CRETZSCHMAR, 1828. [Internet] [Doctoral dissertation]. Paris, EPHE; Université des sciences et de la technologie Houari Boumediene (Alger); 2015. [cited 2020 Oct 27]. Available from: http://www.theses.fr/2015EPHE3011.

Council of Science Editors:

Menad R. Régulation fonctionnelle de l’épididyme d’un rongeur déserticole, Psammomys obesus, CRETZSCHMAR, 1828 : Functional Regulation of Epididymis of Sand Rat Psammomys obesus, CRETZSCHMAR, 1828. [Doctoral Dissertation]. Paris, EPHE; Université des sciences et de la technologie Houari Boumediene (Alger); 2015. Available from: http://www.theses.fr/2015EPHE3011


Tampere University

2. Ahola, Tytti. The Role of Membrane-Initiated Signalling in Progestin-Induced Growth Inhibition in Mammary Epithelial and Breast Cancer Cells .

Degree: Lääketieteen laitos - Medical School, 2004, Tampere University

 Progesteronin synteettistä muotoa progestiinia käytetään laajalti rintasyövän hoidossa, osana hormonikorvaushoitoa ja hormonaalista ehkäisyä. Viimeaikaiset tutkimukset hormonikorvaushoidoista kuitenkin osoittavat, että progestiini lisää rintasyövän riskiä. Tämän johdosta… (more)

Subjects/Keywords: progestiini ; GPR30 ; rintasyöpäsolut ; progestin ; GPR30 ; breast cancer cells

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APA (6th Edition):

Ahola, T. (2004). The Role of Membrane-Initiated Signalling in Progestin-Induced Growth Inhibition in Mammary Epithelial and Breast Cancer Cells . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/67383

Chicago Manual of Style (16th Edition):

Ahola, Tytti. “The Role of Membrane-Initiated Signalling in Progestin-Induced Growth Inhibition in Mammary Epithelial and Breast Cancer Cells .” 2004. Doctoral Dissertation, Tampere University. Accessed October 27, 2020. https://trepo.tuni.fi/handle/10024/67383.

MLA Handbook (7th Edition):

Ahola, Tytti. “The Role of Membrane-Initiated Signalling in Progestin-Induced Growth Inhibition in Mammary Epithelial and Breast Cancer Cells .” 2004. Web. 27 Oct 2020.

Vancouver:

Ahola T. The Role of Membrane-Initiated Signalling in Progestin-Induced Growth Inhibition in Mammary Epithelial and Breast Cancer Cells . [Internet] [Doctoral dissertation]. Tampere University; 2004. [cited 2020 Oct 27]. Available from: https://trepo.tuni.fi/handle/10024/67383.

Council of Science Editors:

Ahola T. The Role of Membrane-Initiated Signalling in Progestin-Induced Growth Inhibition in Mammary Epithelial and Breast Cancer Cells . [Doctoral Dissertation]. Tampere University; 2004. Available from: https://trepo.tuni.fi/handle/10024/67383


Temple University

3. Deliu, Elena. GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation.

Degree: PhD, 2012, Temple University

Pharmacology

The G protein-coupled estrogen receptor GPER/GPER1, also known as GPR30, was originally cloned as an orphan receptor and later shown to be specifically activated… (more)

Subjects/Keywords: Pharmacology; Biochemistry; calcium imaging; estrogen; gpr30; pain; reactive oxygen species

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APA (6th Edition):

Deliu, E. (2012). GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,194862

Chicago Manual of Style (16th Edition):

Deliu, Elena. “GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation.” 2012. Doctoral Dissertation, Temple University. Accessed October 27, 2020. http://digital.library.temple.edu/u?/p245801coll10,194862.

MLA Handbook (7th Edition):

Deliu, Elena. “GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation.” 2012. Web. 27 Oct 2020.

Vancouver:

Deliu E. GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation. [Internet] [Doctoral dissertation]. Temple University; 2012. [cited 2020 Oct 27]. Available from: http://digital.library.temple.edu/u?/p245801coll10,194862.

Council of Science Editors:

Deliu E. GPER/GPR30 Estrogen Receptor: A Target for Pain Modulation. [Doctoral Dissertation]. Temple University; 2012. Available from: http://digital.library.temple.edu/u?/p245801coll10,194862


Freie Universität Berlin

4. Alscher, Sandra. Structure activity relationship studies on G1, the first selective GPR30 agonist.

Degree: 2012, Freie Universität Berlin

 The discovery of the first GPR30 agonist G1 motivates for further research on estrogens and their receptors. New compounds which selectively bind to GPR30 either… (more)

Subjects/Keywords: G1-Analogs, GPR30; cytotoxicity; estrogenicity; 500 Naturwissenschaften und Mathematik::540 Chemie

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APA (6th Edition):

Alscher, S. (2012). Structure activity relationship studies on G1, the first selective GPR30 agonist. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-4864

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):

Alscher, Sandra. “Structure activity relationship studies on G1, the first selective GPR30 agonist.” 2012. Thesis, Freie Universität Berlin. Accessed October 27, 2020. http://dx.doi.org/10.17169/refubium-4864.

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

MLA Handbook (7th Edition):

Alscher, Sandra. “Structure activity relationship studies on G1, the first selective GPR30 agonist.” 2012. Web. 27 Oct 2020.

Vancouver:

Alscher S. Structure activity relationship studies on G1, the first selective GPR30 agonist. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2020 Oct 27]. Available from: http://dx.doi.org/10.17169/refubium-4864.

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

Council of Science Editors:

Alscher S. Structure activity relationship studies on G1, the first selective GPR30 agonist. [Thesis]. Freie Universität Berlin; 2012. Available from: http://dx.doi.org/10.17169/refubium-4864

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


University of New Mexico

5. Scaling, Allison. Characterization of G protein-coupled estrogen receptor (GPER) in breast epithelial proliferation and morphogenesis.

Degree: Biomedical Sciences Graduate Program, 2012, University of New Mexico

  Estrogen (17β-estradiol, E2) plays an important role in regulating an array of functions in both male and female reproductive physiology. In the mammary gland,… (more)

Subjects/Keywords: "GPER; GPR30; Estrogen; Estrogen Receptor; Breast; Proliferation"; Medicine and Health Sciences

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APA (6th Edition):

Scaling, A. (2012). Characterization of G protein-coupled estrogen receptor (GPER) in breast epithelial proliferation and morphogenesis. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/57

Chicago Manual of Style (16th Edition):

Scaling, Allison. “Characterization of G protein-coupled estrogen receptor (GPER) in breast epithelial proliferation and morphogenesis.” 2012. Doctoral Dissertation, University of New Mexico. Accessed October 27, 2020. https://digitalrepository.unm.edu/biom_etds/57.

MLA Handbook (7th Edition):

Scaling, Allison. “Characterization of G protein-coupled estrogen receptor (GPER) in breast epithelial proliferation and morphogenesis.” 2012. Web. 27 Oct 2020.

Vancouver:

Scaling A. Characterization of G protein-coupled estrogen receptor (GPER) in breast epithelial proliferation and morphogenesis. [Internet] [Doctoral dissertation]. University of New Mexico; 2012. [cited 2020 Oct 27]. Available from: https://digitalrepository.unm.edu/biom_etds/57.

Council of Science Editors:

Scaling A. Characterization of G protein-coupled estrogen receptor (GPER) in breast epithelial proliferation and morphogenesis. [Doctoral Dissertation]. University of New Mexico; 2012. Available from: https://digitalrepository.unm.edu/biom_etds/57


University of Kansas

6. McAllister, Carrie E. Estradiol-induced desensitization of 5-HT1A receptor signaling.

Degree: PhD, Neurosciences, 2013, University of Kansas

 Depression is a common psychiatric illness, affecting over 120 million people worldwide. Women are affected disproportionately compared to men, and a large body of clinical… (more)

Subjects/Keywords: Neurosciences; 5-HT1A receptor; Estradiol; G-1; GPR30; RGSz1; sumoylation

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APA (6th Edition):

McAllister, C. E. (2013). Estradiol-induced desensitization of 5-HT1A receptor signaling. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21627

Chicago Manual of Style (16th Edition):

McAllister, Carrie E. “Estradiol-induced desensitization of 5-HT1A receptor signaling.” 2013. Doctoral Dissertation, University of Kansas. Accessed October 27, 2020. http://hdl.handle.net/1808/21627.

MLA Handbook (7th Edition):

McAllister, Carrie E. “Estradiol-induced desensitization of 5-HT1A receptor signaling.” 2013. Web. 27 Oct 2020.

Vancouver:

McAllister CE. Estradiol-induced desensitization of 5-HT1A receptor signaling. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1808/21627.

Council of Science Editors:

McAllister CE. Estradiol-induced desensitization of 5-HT1A receptor signaling. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/21627


Tampere University

7. Purmonen, Sami. Progesterone Target Genes in Breast Cancer Cells .

Degree: 2015, Tampere University

 Progesteronin kohdegeenit rintasyöpäsoluissa Progesteroni l. keltarauhashormoni on pääasiassa munasarjoista ja istukasta erittyvä steroidihormoni, joka yhdessä estrogeenin kanssa säätelee merkittävästi lisääntymisbiologisia tapahtumia. Progesteronin synteettisiä muotoja progestiineja… (more)

Subjects/Keywords: progesteroni ; rintasyöpä ; DLG5 ; GPR30 ; S100P ; progesterone ; breast cancer

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APA (6th Edition):

Purmonen, S. (2015). Progesterone Target Genes in Breast Cancer Cells . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/98038

Chicago Manual of Style (16th Edition):

Purmonen, Sami. “Progesterone Target Genes in Breast Cancer Cells .” 2015. Doctoral Dissertation, Tampere University. Accessed October 27, 2020. https://trepo.tuni.fi/handle/10024/98038.

MLA Handbook (7th Edition):

Purmonen, Sami. “Progesterone Target Genes in Breast Cancer Cells .” 2015. Web. 27 Oct 2020.

Vancouver:

Purmonen S. Progesterone Target Genes in Breast Cancer Cells . [Internet] [Doctoral dissertation]. Tampere University; 2015. [cited 2020 Oct 27]. Available from: https://trepo.tuni.fi/handle/10024/98038.

Council of Science Editors:

Purmonen S. Progesterone Target Genes in Breast Cancer Cells . [Doctoral Dissertation]. Tampere University; 2015. Available from: https://trepo.tuni.fi/handle/10024/98038

8. Nasiri - Ansari, Narjes. Effects of estrogens on endothelial - derived factors implicated in the atherosclerotic plaque vulnerability: clarification of the molecular mechanisms.

Degree: 2017, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 Introduction: Pre-menopausal women have a significantly lower risk for cardiovascular disease while postmenopausal women and women with impaired ovarian function have a greater chance of… (more)

Subjects/Keywords: Αθηρωμάτωση; Φλεγμονές; Οιστρογόνα; HAECS; p21; ER-α; ER-β; GPR30; TNF-α; Atherosclerotic plaques; Inflammation; Estrogen; HAECS; p21; ER-α; ER-β; GPR30; TNF-α

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APA (6th Edition):

Nasiri - Ansari, N. (2017). Effects of estrogens on endothelial - derived factors implicated in the atherosclerotic plaque vulnerability: clarification of the molecular mechanisms. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/41697

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):

Nasiri - Ansari, Narjes. “Effects of estrogens on endothelial - derived factors implicated in the atherosclerotic plaque vulnerability: clarification of the molecular mechanisms.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 27, 2020. http://hdl.handle.net/10442/hedi/41697.

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

MLA Handbook (7th Edition):

Nasiri - Ansari, Narjes. “Effects of estrogens on endothelial - derived factors implicated in the atherosclerotic plaque vulnerability: clarification of the molecular mechanisms.” 2017. Web. 27 Oct 2020.

Vancouver:

Nasiri - Ansari N. Effects of estrogens on endothelial - derived factors implicated in the atherosclerotic plaque vulnerability: clarification of the molecular mechanisms. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10442/hedi/41697.

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

Council of Science Editors:

Nasiri - Ansari N. Effects of estrogens on endothelial - derived factors implicated in the atherosclerotic plaque vulnerability: clarification of the molecular mechanisms. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/41697

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

9. Filipe, Juliana Faria. Estudo do efeito do Octilmetoxicinamato (OMC) em artérias umbilicais humanas.

Degree: 2016, RCAAP

Introdução: O octilmetoxicinamato é um dos filtros de radiação ultravioleta B mais utilizados em protetores solares e produtos cosméticos. Após alguns estudos in vitro e… (more)

Subjects/Keywords: Octilmetoxicinamato · Disruptor Endócrino · Artéria Umbilical Humana · Estrogénio · Gpr30; Domínio/Área Científica::Ciências Médicas::Ciências da Saúde

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APA (6th Edition):

Filipe, J. F. (2016). Estudo do efeito do Octilmetoxicinamato (OMC) em artérias umbilicais humanas. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5364

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):

Filipe, Juliana Faria. “Estudo do efeito do Octilmetoxicinamato (OMC) em artérias umbilicais humanas.” 2016. Thesis, RCAAP. Accessed October 27, 2020. https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5364.

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

MLA Handbook (7th Edition):

Filipe, Juliana Faria. “Estudo do efeito do Octilmetoxicinamato (OMC) em artérias umbilicais humanas.” 2016. Web. 27 Oct 2020.

Vancouver:

Filipe JF. Estudo do efeito do Octilmetoxicinamato (OMC) em artérias umbilicais humanas. [Internet] [Thesis]. RCAAP; 2016. [cited 2020 Oct 27]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5364.

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

Council of Science Editors:

Filipe JF. Estudo do efeito do Octilmetoxicinamato (OMC) em artérias umbilicais humanas. [Thesis]. RCAAP; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:ubibliorum.ubi.pt:10400.6/5364

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


University of Guelph

10. 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 October 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 Oct 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 Oct 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

11. Rafi, Ali. Estrogen action in growth plate cartilage.

Degree: Life Sciences, 2011, University of Skövde

Subjects/Keywords: Estrogen; growth plate; GPR30; GPER; IGF-1

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APA (6th Edition):

Rafi, A. (2011). Estrogen action in growth plate cartilage. (Thesis). University of Skövde. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-5463

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):

Rafi, Ali. “Estrogen action in growth plate cartilage.” 2011. Thesis, University of Skövde. Accessed October 27, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-5463.

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

MLA Handbook (7th Edition):

Rafi, Ali. “Estrogen action in growth plate cartilage.” 2011. Web. 27 Oct 2020.

Vancouver:

Rafi A. Estrogen action in growth plate cartilage. [Internet] [Thesis]. University of Skövde; 2011. [cited 2020 Oct 27]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-5463.

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

Council of Science Editors:

Rafi A. Estrogen action in growth plate cartilage. [Thesis]. University of Skövde; 2011. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-5463

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


University of Kansas

12. Liverman, Christopher S. Estrogen Signaling in Trigeminal Nociception.

Degree: PhD, Anatomy & Cell Biology, 2008, University of Kansas

 Migraine is much more common in women than in men, and painful episodes are linked to the hormonal fluctuations of the menstrual cycle. The MAP… (more)

Subjects/Keywords: Biology; Neurosciences; Erk; Estrogen; Gpr30; Trigeminal ganglion

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APA (6th Edition):

Liverman, C. S. (2008). Estrogen Signaling in Trigeminal Nociception. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/4327

Chicago Manual of Style (16th Edition):

Liverman, Christopher S. “Estrogen Signaling in Trigeminal Nociception.” 2008. Doctoral Dissertation, University of Kansas. Accessed October 27, 2020. http://hdl.handle.net/1808/4327.

MLA Handbook (7th Edition):

Liverman, Christopher S. “Estrogen Signaling in Trigeminal Nociception.” 2008. Web. 27 Oct 2020.

Vancouver:

Liverman CS. Estrogen Signaling in Trigeminal Nociception. [Internet] [Doctoral dissertation]. University of Kansas; 2008. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1808/4327.

Council of Science Editors:

Liverman CS. Estrogen Signaling in Trigeminal Nociception. [Doctoral Dissertation]. University of Kansas; 2008. Available from: http://hdl.handle.net/1808/4327

13. Liu, Bonan. The role of GRK2 in hypertension and regulation of GPR30.

Degree: 2012, University of Western Ontario

 In the hypertensive state, the expression of G protein-coupled receptor kinase 2 (GRK2) level is elevated. On the other hand, the expression of GPR30, a… (more)

Subjects/Keywords: GRK2; hypertension; GPR30; vascular; G protein signaling; Pharmacology

…2.10 GPR30 protein expression in heart, aorta and VSMCs.................................. 44… …50 2.14 Co-immunoprecipitation of GPR30 and GRK2… …66 3.6 GPR30 protein expression in heart and aorta tissues as well as cultured VSMCs… …69 3.7 Assessment of GPR30 mediated vascular reactivity in aortic rings .............. 73… …3.8 The effects of GPR30 agonist in cultured EC… 

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APA (6th Edition):

Liu, B. (2012). The role of GRK2 in hypertension and regulation of GPR30. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/578

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):

Liu, Bonan. “The role of GRK2 in hypertension and regulation of GPR30.” 2012. Thesis, University of Western Ontario. Accessed October 27, 2020. https://ir.lib.uwo.ca/etd/578.

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

MLA Handbook (7th Edition):

Liu, Bonan. “The role of GRK2 in hypertension and regulation of GPR30.” 2012. Web. 27 Oct 2020.

Vancouver:

Liu B. The role of GRK2 in hypertension and regulation of GPR30. [Internet] [Thesis]. University of Western Ontario; 2012. [cited 2020 Oct 27]. Available from: https://ir.lib.uwo.ca/etd/578.

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

Council of Science Editors:

Liu B. The role of GRK2 in hypertension and regulation of GPR30. [Thesis]. University of Western Ontario; 2012. Available from: https://ir.lib.uwo.ca/etd/578

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


University of Lund

14. Broselid, Stefan. The G protein-coupled receptor GPR30 signalosome - A novel G protein-independent mechanism regulating cAMP signaling and receptor trafficking.

Degree: 2014, University of Lund

 The large protein family called G Protein-coupled receptors (GPCRs) has co-evolved with life throughout evolution; from single cell organisms all the way to complex beings… (more)

Subjects/Keywords: Pharmacology and Toxicology; AKAP5; AKAP; MAGUK; cAMP signaling; constitutive signaling; signalosome; GPER; GPR30; GPCR; cytokeratin; RAMP3; apoptotic signaling; breast cancer; PDZ; PDZ-ligand

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

APA (6th Edition):

Broselid, S. (2014). The G protein-coupled receptor GPR30 signalosome - A novel G protein-independent mechanism regulating cAMP signaling and receptor trafficking. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/4858362 ; https://portal.research.lu.se/ws/files/4203594/4858383.pdf

Chicago Manual of Style (16th Edition):

Broselid, Stefan. “The G protein-coupled receptor GPR30 signalosome - A novel G protein-independent mechanism regulating cAMP signaling and receptor trafficking.” 2014. Doctoral Dissertation, University of Lund. Accessed October 27, 2020. https://lup.lub.lu.se/record/4858362 ; https://portal.research.lu.se/ws/files/4203594/4858383.pdf.

MLA Handbook (7th Edition):

Broselid, Stefan. “The G protein-coupled receptor GPR30 signalosome - A novel G protein-independent mechanism regulating cAMP signaling and receptor trafficking.” 2014. Web. 27 Oct 2020.

Vancouver:

Broselid S. The G protein-coupled receptor GPR30 signalosome - A novel G protein-independent mechanism regulating cAMP signaling and receptor trafficking. [Internet] [Doctoral dissertation]. University of Lund; 2014. [cited 2020 Oct 27]. Available from: https://lup.lub.lu.se/record/4858362 ; https://portal.research.lu.se/ws/files/4203594/4858383.pdf.

Council of Science Editors:

Broselid S. The G protein-coupled receptor GPR30 signalosome - A novel G protein-independent mechanism regulating cAMP signaling and receptor trafficking. [Doctoral Dissertation]. University of Lund; 2014. Available from: https://lup.lub.lu.se/record/4858362 ; https://portal.research.lu.se/ws/files/4203594/4858383.pdf


University of New Mexico

15. Dennis, Megan. Identification and characterization of steroid receptor ligands.

Degree: Biomedical Sciences Graduate Program, 2010, University of New Mexico

 This work focuses on steroid receptors, including the androgen receptor (AR), the estrogen receptors (ERs) ERα and ERβ, known as the classical ERs, and GPR30,… (more)

Subjects/Keywords: Estrogen; Androgen; GPR30; GPER; Small molecule discovery; High throughput screening

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APA (6th Edition):

Dennis, M. (2010). Identification and characterization of steroid receptor ligands. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/11

Chicago Manual of Style (16th Edition):

Dennis, Megan. “Identification and characterization of steroid receptor ligands.” 2010. Doctoral Dissertation, University of New Mexico. Accessed October 27, 2020. https://digitalrepository.unm.edu/biom_etds/11.

MLA Handbook (7th Edition):

Dennis, Megan. “Identification and characterization of steroid receptor ligands.” 2010. Web. 27 Oct 2020.

Vancouver:

Dennis M. Identification and characterization of steroid receptor ligands. [Internet] [Doctoral dissertation]. University of New Mexico; 2010. [cited 2020 Oct 27]. Available from: https://digitalrepository.unm.edu/biom_etds/11.

Council of Science Editors:

Dennis M. Identification and characterization of steroid receptor ligands. [Doctoral Dissertation]. University of New Mexico; 2010. Available from: https://digitalrepository.unm.edu/biom_etds/11


University of South Carolina

16. Balapanage, Sumith Jayasinghe. G-Protein-Coupled Estrogen Receptor-1 (GPER): A Potential Target For Xenoestrogens During Vertebrate Embryogenesis.

Degree: PhD, Environmental Health Sciences, 2012, University of South Carolina

  G-protein-coupled estrogen receptor 1 (GPER) is a G-protein-coupled receptor that induces non-genomic signaling in response to some nuclear estrogen receptor ligands. To date, the… (more)

Subjects/Keywords: Environmental Health; Environmental Sciences; Life Sciences; Pharmacology, Toxicology and Environmental Health; Physical Sciences and Mathematics; cardiovascular impairments; Developmental toxicology; endocrine distruption; GPER/ GPR30; ligand-induced activation; Zebrafish embryogenesis

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

APA (6th Edition):

Balapanage, S. J. (2012). G-Protein-Coupled Estrogen Receptor-1 (GPER): A Potential Target For Xenoestrogens During Vertebrate Embryogenesis. (Doctoral Dissertation). University of South Carolina. Retrieved from https://scholarcommons.sc.edu/etd/1114

Chicago Manual of Style (16th Edition):

Balapanage, Sumith Jayasinghe. “G-Protein-Coupled Estrogen Receptor-1 (GPER): A Potential Target For Xenoestrogens During Vertebrate Embryogenesis.” 2012. Doctoral Dissertation, University of South Carolina. Accessed October 27, 2020. https://scholarcommons.sc.edu/etd/1114.

MLA Handbook (7th Edition):

Balapanage, Sumith Jayasinghe. “G-Protein-Coupled Estrogen Receptor-1 (GPER): A Potential Target For Xenoestrogens During Vertebrate Embryogenesis.” 2012. Web. 27 Oct 2020.

Vancouver:

Balapanage SJ. G-Protein-Coupled Estrogen Receptor-1 (GPER): A Potential Target For Xenoestrogens During Vertebrate Embryogenesis. [Internet] [Doctoral dissertation]. University of South Carolina; 2012. [cited 2020 Oct 27]. Available from: https://scholarcommons.sc.edu/etd/1114.

Council of Science Editors:

Balapanage SJ. G-Protein-Coupled Estrogen Receptor-1 (GPER): A Potential Target For Xenoestrogens During Vertebrate Embryogenesis. [Doctoral Dissertation]. University of South Carolina; 2012. Available from: https://scholarcommons.sc.edu/etd/1114


Universidade do Rio Grande do Sul

17. Santin, Ana Paula. Estudo de hormônios sexuais em células foliculares de tireoide humana em cultura primária.

Degree: 2012, Universidade do Rio Grande do Sul

Os mecanismos etiopatogênicos que levam ao desenvolvimento dos nódulos e tumores da tireoide ainda não são bem conhecidos. É fato estabelecido que a prevalência dessas… (more)

Subjects/Keywords: Glândula tireóide; Thyroid; Primary culture; Cultura primária de células; Células dendríticas foliculares; Follicular thyroid cell; Hormônios gonadais; Thyroperoxidase; Thyroglobulin; Sodium/iodide simporter; Reference gene; Progesterone; Estradiol; Progesterone receptor; Estrogen receptor; GPR30

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

APA (6th Edition):

Santin, A. P. (2012). Estudo de hormônios sexuais em células foliculares de tireoide humana em cultura primária. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/69639

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):

Santin, Ana Paula. “Estudo de hormônios sexuais em células foliculares de tireoide humana em cultura primária.” 2012. Thesis, Universidade do Rio Grande do Sul. Accessed October 27, 2020. http://hdl.handle.net/10183/69639.

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

MLA Handbook (7th Edition):

Santin, Ana Paula. “Estudo de hormônios sexuais em células foliculares de tireoide humana em cultura primária.” 2012. Web. 27 Oct 2020.

Vancouver:

Santin AP. Estudo de hormônios sexuais em células foliculares de tireoide humana em cultura primária. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10183/69639.

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

Council of Science Editors:

Santin AP. Estudo de hormônios sexuais em células foliculares de tireoide humana em cultura primária. [Thesis]. Universidade do Rio Grande do Sul; 2012. Available from: http://hdl.handle.net/10183/69639

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


Freie Universität Berlin

18. Malek, Daniela. Einfluss auf die Migration humaner Mammakarzinomzellen.

Degree: 2007, Freie Universität Berlin

 Estrogene spielen eine wichtige Rolle bei einer Vielzahl physiologischer Prozesse, wie Fortpflanzung und Verhalten, sind aber auch bei Entstehung und Fortschreiten pathologischer Prozesse beteiligt. So… (more)

Subjects/Keywords: estradiol TGF-ß GPR30 MCF-7 migration; 500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete Wissenschaften

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

APA (6th Edition):

Malek, D. (2007). Einfluss auf die Migration humaner Mammakarzinomzellen. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-9917

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):

Malek, Daniela. “Einfluss auf die Migration humaner Mammakarzinomzellen.” 2007. Thesis, Freie Universität Berlin. Accessed October 27, 2020. http://dx.doi.org/10.17169/refubium-9917.

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

MLA Handbook (7th Edition):

Malek, Daniela. “Einfluss auf die Migration humaner Mammakarzinomzellen.” 2007. Web. 27 Oct 2020.

Vancouver:

Malek D. Einfluss auf die Migration humaner Mammakarzinomzellen. [Internet] [Thesis]. Freie Universität Berlin; 2007. [cited 2020 Oct 27]. Available from: http://dx.doi.org/10.17169/refubium-9917.

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

Council of Science Editors:

Malek D. Einfluss auf die Migration humaner Mammakarzinomzellen. [Thesis]. Freie Universität Berlin; 2007. Available from: http://dx.doi.org/10.17169/refubium-9917

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


University of Lund

19. Henic, Emir. The uPA receptor in ovarian cancer. Regulation by EGF and the estrogen responsive membrane receptor GPR30. Soluble uPAR in diagnosis and prognosis.

Degree: 2008, University of Lund

 Cell migration is the first step of the invasive process, which is part of the malignant phenotype, and the uPA receptor (uPAR) plays a central… (more)

Subjects/Keywords: Obstetrics, Gynecology and Reproductive Medicine; G-1.; GPR30; suPAR; prognosis; estradiol; ovarian cancer; EGFR; ER; diagnosis

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

APA (6th Edition):

Henic, E. (2008). The uPA receptor in ovarian cancer. Regulation by EGF and the estrogen responsive membrane receptor GPR30. Soluble uPAR in diagnosis and prognosis. (Doctoral Dissertation). University of Lund. Retrieved from https://lup.lub.lu.se/record/1259364 ; https://portal.research.lu.se/ws/files/4007119/1259782.pdf

Chicago Manual of Style (16th Edition):

Henic, Emir. “The uPA receptor in ovarian cancer. Regulation by EGF and the estrogen responsive membrane receptor GPR30. Soluble uPAR in diagnosis and prognosis.” 2008. Doctoral Dissertation, University of Lund. Accessed October 27, 2020. https://lup.lub.lu.se/record/1259364 ; https://portal.research.lu.se/ws/files/4007119/1259782.pdf.

MLA Handbook (7th Edition):

Henic, Emir. “The uPA receptor in ovarian cancer. Regulation by EGF and the estrogen responsive membrane receptor GPR30. Soluble uPAR in diagnosis and prognosis.” 2008. Web. 27 Oct 2020.

Vancouver:

Henic E. The uPA receptor in ovarian cancer. Regulation by EGF and the estrogen responsive membrane receptor GPR30. Soluble uPAR in diagnosis and prognosis. [Internet] [Doctoral dissertation]. University of Lund; 2008. [cited 2020 Oct 27]. Available from: https://lup.lub.lu.se/record/1259364 ; https://portal.research.lu.se/ws/files/4007119/1259782.pdf.

Council of Science Editors:

Henic E. The uPA receptor in ovarian cancer. Regulation by EGF and the estrogen responsive membrane receptor GPR30. Soluble uPAR in diagnosis and prognosis. [Doctoral Dissertation]. University of Lund; 2008. Available from: https://lup.lub.lu.se/record/1259364 ; https://portal.research.lu.se/ws/files/4007119/1259782.pdf

.