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You searched for subject:(Tamoxifen). Showing records 1 – 30 of 184 total matches.

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University of Alberta

1. Cole, Laura Kathleen. Insights into the Transcriptional Regulation and Physiological Importance of Phosphatidylethanolamine N-Methyltransferase.

Degree: PhD, Department of Biochemistry, 2010, University of Alberta

 Phosphatidylcholine (PC) is made in all nucleated mammalian cells via the CDP-choline pathway. Another major pathway for PC biosynthesis in liver is catalyzed by phosphatidylethanolamine… (more)

Subjects/Keywords: Tamoxifen; Sp1; Phosphatidylcholine; Cardiac Dysfunction

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

APA (6th Edition):

Cole, L. K. (2010). Insights into the Transcriptional Regulation and Physiological Importance of Phosphatidylethanolamine N-Methyltransferase. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/m900nt98v

Chicago Manual of Style (16th Edition):

Cole, Laura Kathleen. “Insights into the Transcriptional Regulation and Physiological Importance of Phosphatidylethanolamine N-Methyltransferase.” 2010. Doctoral Dissertation, University of Alberta. Accessed January 28, 2021. https://era.library.ualberta.ca/files/m900nt98v.

MLA Handbook (7th Edition):

Cole, Laura Kathleen. “Insights into the Transcriptional Regulation and Physiological Importance of Phosphatidylethanolamine N-Methyltransferase.” 2010. Web. 28 Jan 2021.

Vancouver:

Cole LK. Insights into the Transcriptional Regulation and Physiological Importance of Phosphatidylethanolamine N-Methyltransferase. [Internet] [Doctoral dissertation]. University of Alberta; 2010. [cited 2021 Jan 28]. Available from: https://era.library.ualberta.ca/files/m900nt98v.

Council of Science Editors:

Cole LK. Insights into the Transcriptional Regulation and Physiological Importance of Phosphatidylethanolamine N-Methyltransferase. [Doctoral Dissertation]. University of Alberta; 2010. Available from: https://era.library.ualberta.ca/files/m900nt98v


Vanderbilt University

2. Reinert, Rachel Byerley. Vascular Endothelial Growth Factor A Coordinates Pancreatic Islet Vascularization, Innervation, and Function.

Degree: PhD, Molecular Physiology and Biophysics, 2012, Vanderbilt University

 Pancreatic islets are miniature endocrine organs that regulate glucose homeostasis. Islets are highly vascularized and richly innervated, but the molecular mechanisms directing this organization are… (more)

Subjects/Keywords: VEGF; Cre-loxP recombination; tamoxifen

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APA (6th Edition):

Reinert, R. B. (2012). Vascular Endothelial Growth Factor A Coordinates Pancreatic Islet Vascularization, Innervation, and Function. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14196

Chicago Manual of Style (16th Edition):

Reinert, Rachel Byerley. “Vascular Endothelial Growth Factor A Coordinates Pancreatic Islet Vascularization, Innervation, and Function.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed January 28, 2021. http://hdl.handle.net/1803/14196.

MLA Handbook (7th Edition):

Reinert, Rachel Byerley. “Vascular Endothelial Growth Factor A Coordinates Pancreatic Islet Vascularization, Innervation, and Function.” 2012. Web. 28 Jan 2021.

Vancouver:

Reinert RB. Vascular Endothelial Growth Factor A Coordinates Pancreatic Islet Vascularization, Innervation, and Function. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/1803/14196.

Council of Science Editors:

Reinert RB. Vascular Endothelial Growth Factor A Coordinates Pancreatic Islet Vascularization, Innervation, and Function. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/14196


University of Texas Southwestern Medical Center

3. Chen, Jian. Malignant Gliomas Originate From Neural Stem/Progenitor Cells and Are Maintained By Cancer Stem Cells.

Degree: 2011, University of Texas Southwestern Medical Center

 Malignant glioma is one of the most aggressive cancers. To study the biology of glioma, our lab previously developed a series of mouse models that… (more)

Subjects/Keywords: Gliomas; Adult Stem Cells; Tamoxifen

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APA (6th Edition):

Chen, J. (2011). Malignant Gliomas Originate From Neural Stem/Progenitor Cells and Are Maintained By Cancer Stem Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/938

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):

Chen, Jian. “Malignant Gliomas Originate From Neural Stem/Progenitor Cells and Are Maintained By Cancer Stem Cells.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed January 28, 2021. http://hdl.handle.net/2152.5/938.

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

MLA Handbook (7th Edition):

Chen, Jian. “Malignant Gliomas Originate From Neural Stem/Progenitor Cells and Are Maintained By Cancer Stem Cells.” 2011. Web. 28 Jan 2021.

Vancouver:

Chen J. Malignant Gliomas Originate From Neural Stem/Progenitor Cells and Are Maintained By Cancer Stem Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/2152.5/938.

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

Council of Science Editors:

Chen J. Malignant Gliomas Originate From Neural Stem/Progenitor Cells and Are Maintained By Cancer Stem Cells. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/938

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


Univerzitet u Beogradu

4. Abu Rabi, Zaki, 1980-. Značaj biološke heterogenosti karcinoma dojke za odgovor na terapiju antiestrogenima.

Degree: Biološki fakultet, 2014, Univerzitet u Beogradu

Molekularna biologija kancera dojke / Molekularna biologija kancera dojke

Karcinom dojke, kao najčešći oblik malignih tumora koji se javlja kod žena, spada u grupu heterogenih… (more)

Subjects/Keywords: breast cancer; tamoxifen; resistance

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APA (6th Edition):

Abu Rabi, Zaki, 1. (2014). Značaj biološke heterogenosti karcinoma dojke za odgovor na terapiju antiestrogenima. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get

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

Chicago Manual of Style (16th Edition):

Abu Rabi, Zaki, 1980-. “Značaj biološke heterogenosti karcinoma dojke za odgovor na terapiju antiestrogenima.” 2014. Thesis, Univerzitet u Beogradu. Accessed January 28, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get.

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

MLA Handbook (7th Edition):

Abu Rabi, Zaki, 1980-. “Značaj biološke heterogenosti karcinoma dojke za odgovor na terapiju antiestrogenima.” 2014. Web. 28 Jan 2021.

Vancouver:

Abu Rabi, Zaki 1. Značaj biološke heterogenosti karcinoma dojke za odgovor na terapiju antiestrogenima. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2021 Jan 28]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get.

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

Council of Science Editors:

Abu Rabi, Zaki 1. Značaj biološke heterogenosti karcinoma dojke za odgovor na terapiju antiestrogenima. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get

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


University of Edinburgh

5. Patel, Saloni Hiten. Inducible gene targeting in the male : tamoxifen adversely impacts postnatal testicular development and function.

Degree: PhD, 2016, University of Edinburgh

 Normal development and function of the male reproductive tract relies on the crucial balance between androgen and estrogen signalling, furthermore estrogens play an important role… (more)

Subjects/Keywords: 612.6; Tamoxifen; testis; Leydig cells

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APA (6th Edition):

Patel, S. H. (2016). Inducible gene targeting in the male : tamoxifen adversely impacts postnatal testicular development and function. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25870

Chicago Manual of Style (16th Edition):

Patel, Saloni Hiten. “Inducible gene targeting in the male : tamoxifen adversely impacts postnatal testicular development and function.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed January 28, 2021. http://hdl.handle.net/1842/25870.

MLA Handbook (7th Edition):

Patel, Saloni Hiten. “Inducible gene targeting in the male : tamoxifen adversely impacts postnatal testicular development and function.” 2016. Web. 28 Jan 2021.

Vancouver:

Patel SH. Inducible gene targeting in the male : tamoxifen adversely impacts postnatal testicular development and function. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/1842/25870.

Council of Science Editors:

Patel SH. Inducible gene targeting in the male : tamoxifen adversely impacts postnatal testicular development and function. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25870


Ruhr Universität Bochum

6. Alemi, Mohammad Aref. Endometriumveränderungen unter Tamoxifen bei Mammakarzinompatientinnen : Korrelation des sonographischen mit dem intraoperativen und histologischen Befund unter Berücksichtigung des endometrialen Rezeptorstatus.

Degree: 2014, Ruhr Universität Bochum

 Problem: In der vorliegenden Arbeit wurde untersucht, inwiefern die sonographische Diagnose mit dem hysteroskopischen und dem histologischen Befund korrelieren. Methode: Es wurden 52 hormonrezeptorpositive Mammakarzinompatientinnen… (more)

Subjects/Keywords: Gebärmutterschleimhaut / Änderung; Tamoxifen; Brustkrebs; Hormonrezeptor; Hysteroskopie

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APA (6th Edition):

Alemi, M. A. (2014). Endometriumveränderungen unter Tamoxifen bei Mammakarzinompatientinnen : Korrelation des sonographischen mit dem intraoperativen und histologischen Befund unter Berücksichtigung des endometrialen Rezeptorstatus. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-42183

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):

Alemi, Mohammad Aref. “Endometriumveränderungen unter Tamoxifen bei Mammakarzinompatientinnen : Korrelation des sonographischen mit dem intraoperativen und histologischen Befund unter Berücksichtigung des endometrialen Rezeptorstatus.” 2014. Thesis, Ruhr Universität Bochum. Accessed January 28, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-42183.

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

MLA Handbook (7th Edition):

Alemi, Mohammad Aref. “Endometriumveränderungen unter Tamoxifen bei Mammakarzinompatientinnen : Korrelation des sonographischen mit dem intraoperativen und histologischen Befund unter Berücksichtigung des endometrialen Rezeptorstatus.” 2014. Web. 28 Jan 2021.

Vancouver:

Alemi MA. Endometriumveränderungen unter Tamoxifen bei Mammakarzinompatientinnen : Korrelation des sonographischen mit dem intraoperativen und histologischen Befund unter Berücksichtigung des endometrialen Rezeptorstatus. [Internet] [Thesis]. Ruhr Universität Bochum; 2014. [cited 2021 Jan 28]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-42183.

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

Council of Science Editors:

Alemi MA. Endometriumveränderungen unter Tamoxifen bei Mammakarzinompatientinnen : Korrelation des sonographischen mit dem intraoperativen und histologischen Befund unter Berücksichtigung des endometrialen Rezeptorstatus. [Thesis]. Ruhr Universität Bochum; 2014. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-42183

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


University of Otago

7. Scandlyn, Marissa Jayne. Novel drug therapies for ER- basal-like breast cancer; preclinical evaluation in a xenograft model.

Degree: 2011, University of Otago

 Basal-like breast cancers are a subgroup of breast lesions that are triple-negative for the estrogen receptor (ER), progesterone receptor and human epidermal growth factor receptor… (more)

Subjects/Keywords: EGCG; Breast cancer; Tamoxifen; Raloxifene; Curcumin

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APA (6th Edition):

Scandlyn, M. J. (2011). Novel drug therapies for ER- basal-like breast cancer; preclinical evaluation in a xenograft model. (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/1688

Chicago Manual of Style (16th Edition):

Scandlyn, Marissa Jayne. “Novel drug therapies for ER- basal-like breast cancer; preclinical evaluation in a xenograft model. ” 2011. Doctoral Dissertation, University of Otago. Accessed January 28, 2021. http://hdl.handle.net/10523/1688.

MLA Handbook (7th Edition):

Scandlyn, Marissa Jayne. “Novel drug therapies for ER- basal-like breast cancer; preclinical evaluation in a xenograft model. ” 2011. Web. 28 Jan 2021.

Vancouver:

Scandlyn MJ. Novel drug therapies for ER- basal-like breast cancer; preclinical evaluation in a xenograft model. [Internet] [Doctoral dissertation]. University of Otago; 2011. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/10523/1688.

Council of Science Editors:

Scandlyn MJ. Novel drug therapies for ER- basal-like breast cancer; preclinical evaluation in a xenograft model. [Doctoral Dissertation]. University of Otago; 2011. Available from: http://hdl.handle.net/10523/1688

8. Nkuliyingoma, Anastase. Effects of Oestrogen Receptor Status of Women with Breast Cancer Treated with Tamoxifen at University Teaching Hospital and Cancer Diseases Hospital.

Degree: 2015, University of Zimbabwe

 The main objective of this study was to determine the prevalence of oestrogen receptor-negative breast cancers at UTH and CDH and its impact on tamoxifen(more)

Subjects/Keywords: Hormone Receptors; Breast – Cancer – Hormone Therapy; Tamoxifen

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APA (6th Edition):

Nkuliyingoma, A. (2015). Effects of Oestrogen Receptor Status of Women with Breast Cancer Treated with Tamoxifen at University Teaching Hospital and Cancer Diseases Hospital. (Thesis). University of Zimbabwe. Retrieved from http://dspace.unza.zm/handle/123456789/4364

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):

Nkuliyingoma, Anastase. “Effects of Oestrogen Receptor Status of Women with Breast Cancer Treated with Tamoxifen at University Teaching Hospital and Cancer Diseases Hospital.” 2015. Thesis, University of Zimbabwe. Accessed January 28, 2021. http://dspace.unza.zm/handle/123456789/4364.

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

MLA Handbook (7th Edition):

Nkuliyingoma, Anastase. “Effects of Oestrogen Receptor Status of Women with Breast Cancer Treated with Tamoxifen at University Teaching Hospital and Cancer Diseases Hospital.” 2015. Web. 28 Jan 2021.

Vancouver:

Nkuliyingoma A. Effects of Oestrogen Receptor Status of Women with Breast Cancer Treated with Tamoxifen at University Teaching Hospital and Cancer Diseases Hospital. [Internet] [Thesis]. University of Zimbabwe; 2015. [cited 2021 Jan 28]. Available from: http://dspace.unza.zm/handle/123456789/4364.

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

Council of Science Editors:

Nkuliyingoma A. Effects of Oestrogen Receptor Status of Women with Breast Cancer Treated with Tamoxifen at University Teaching Hospital and Cancer Diseases Hospital. [Thesis]. University of Zimbabwe; 2015. Available from: http://dspace.unza.zm/handle/123456789/4364

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


University of Aberdeen

9. Maley, Mary. The role of individual forms of cytochrome P450 in drug metabolism in human liver microsomes.

Degree: PhD, 1996, University of Aberdeen

 Human liver microsomal metabolism of nicardipine was investigated and compared to that of another dihydropyridine, felodipine, and to published results for other compounds belonging to… (more)

Subjects/Keywords: 572; Cytochrome; Tamoxifen

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APA (6th Edition):

Maley, M. (1996). The role of individual forms of cytochrome P450 in drug metabolism in human liver microsomes. (Doctoral Dissertation). University of Aberdeen. Retrieved from https://eu03.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886690005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327540

Chicago Manual of Style (16th Edition):

Maley, Mary. “The role of individual forms of cytochrome P450 in drug metabolism in human liver microsomes.” 1996. Doctoral Dissertation, University of Aberdeen. Accessed January 28, 2021. https://eu03.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886690005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327540.

MLA Handbook (7th Edition):

Maley, Mary. “The role of individual forms of cytochrome P450 in drug metabolism in human liver microsomes.” 1996. Web. 28 Jan 2021.

Vancouver:

Maley M. The role of individual forms of cytochrome P450 in drug metabolism in human liver microsomes. [Internet] [Doctoral dissertation]. University of Aberdeen; 1996. [cited 2021 Jan 28]. Available from: https://eu03.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886690005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327540.

Council of Science Editors:

Maley M. The role of individual forms of cytochrome P450 in drug metabolism in human liver microsomes. [Doctoral Dissertation]. University of Aberdeen; 1996. Available from: https://eu03.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152886690005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327540


University of Southern California

10. Schafer, Christopher A. The temporal and tissue specific requirement of Msx genes in murine skull vault osteogenesis.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2011, University of Southern California

 The homeobox genes Msx1 and Msx2 are set of transcription factors known to have both widespread and overlapping expression patterns throughout the developing murine embryo.… (more)

Subjects/Keywords: skull vault; neural crest; mesoderm; tamoxifen

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APA (6th Edition):

Schafer, C. A. (2011). The temporal and tissue specific requirement of Msx genes in murine skull vault osteogenesis. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/636188/rec/7353

Chicago Manual of Style (16th Edition):

Schafer, Christopher A. “The temporal and tissue specific requirement of Msx genes in murine skull vault osteogenesis.” 2011. Doctoral Dissertation, University of Southern California. Accessed January 28, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/636188/rec/7353.

MLA Handbook (7th Edition):

Schafer, Christopher A. “The temporal and tissue specific requirement of Msx genes in murine skull vault osteogenesis.” 2011. Web. 28 Jan 2021.

Vancouver:

Schafer CA. The temporal and tissue specific requirement of Msx genes in murine skull vault osteogenesis. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2021 Jan 28]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/636188/rec/7353.

Council of Science Editors:

Schafer CA. The temporal and tissue specific requirement of Msx genes in murine skull vault osteogenesis. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/636188/rec/7353


University of Southern California

11. Gordon, Michael Alexander. HER2 and co-amplified genes in breast and gastric cancer.

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

 Breast cancer is a heterogeneous disease containing numerous subtypes with disparate outcomes. Patients whose breast cancers contain HER2 gene amplification have a significantly worse prognosis;… (more)

Subjects/Keywords: breast cancer; gastric cancer; HER2; MYST2; tamoxifen

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APA (6th Edition):

Gordon, M. A. (2013). HER2 and co-amplified genes in breast and gastric cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/315085/rec/3156

Chicago Manual of Style (16th Edition):

Gordon, Michael Alexander. “HER2 and co-amplified genes in breast and gastric cancer.” 2013. Doctoral Dissertation, University of Southern California. Accessed January 28, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/315085/rec/3156.

MLA Handbook (7th Edition):

Gordon, Michael Alexander. “HER2 and co-amplified genes in breast and gastric cancer.” 2013. Web. 28 Jan 2021.

Vancouver:

Gordon MA. HER2 and co-amplified genes in breast and gastric cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Jan 28]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/315085/rec/3156.

Council of Science Editors:

Gordon MA. HER2 and co-amplified genes in breast and gastric cancer. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/315085/rec/3156


Duke University

12. Ogburn, Ryenne. Development of Data Analysis Methods and Applications for Proteome-Wide SPROX Measurements .

Degree: 2017, Duke University

  Protein-ligand interactions can be detected and quantified using protein folding stability measurements. Thus, protein folding stability changes are closely linked to protein function and… (more)

Subjects/Keywords: Biochemistry; Chemistry; allergens; Proteomics; SPROX; tamoxifen

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APA (6th Edition):

Ogburn, R. (2017). Development of Data Analysis Methods and Applications for Proteome-Wide SPROX Measurements . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/16251

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):

Ogburn, Ryenne. “Development of Data Analysis Methods and Applications for Proteome-Wide SPROX Measurements .” 2017. Thesis, Duke University. Accessed January 28, 2021. http://hdl.handle.net/10161/16251.

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

MLA Handbook (7th Edition):

Ogburn, Ryenne. “Development of Data Analysis Methods and Applications for Proteome-Wide SPROX Measurements .” 2017. Web. 28 Jan 2021.

Vancouver:

Ogburn R. Development of Data Analysis Methods and Applications for Proteome-Wide SPROX Measurements . [Internet] [Thesis]. Duke University; 2017. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/10161/16251.

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

Council of Science Editors:

Ogburn R. Development of Data Analysis Methods and Applications for Proteome-Wide SPROX Measurements . [Thesis]. Duke University; 2017. Available from: http://hdl.handle.net/10161/16251

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


Clemson University

13. Elraghy, Omaima. REPRESSION OF MULTIPLE CYP2D GENES IN MOUSE USING A SINGLE SIRNA CONSTRUCT.

Degree: MS, Biological Sciences, 2011, Clemson University

 The CYP2D subfamily is the second most important subfamily of hepatic drug metabolizing CYPs. In mouse, there are nine CYP2D subfamily members, while humans have… (more)

Subjects/Keywords: CYP2D; P450; siRNA; Tamoxifen; Testosterone; Biology

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APA (6th Edition):

Elraghy, O. (2011). REPRESSION OF MULTIPLE CYP2D GENES IN MOUSE USING A SINGLE SIRNA CONSTRUCT. (Masters Thesis). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_theses/1149

Chicago Manual of Style (16th Edition):

Elraghy, Omaima. “REPRESSION OF MULTIPLE CYP2D GENES IN MOUSE USING A SINGLE SIRNA CONSTRUCT.” 2011. Masters Thesis, Clemson University. Accessed January 28, 2021. https://tigerprints.clemson.edu/all_theses/1149.

MLA Handbook (7th Edition):

Elraghy, Omaima. “REPRESSION OF MULTIPLE CYP2D GENES IN MOUSE USING A SINGLE SIRNA CONSTRUCT.” 2011. Web. 28 Jan 2021.

Vancouver:

Elraghy O. REPRESSION OF MULTIPLE CYP2D GENES IN MOUSE USING A SINGLE SIRNA CONSTRUCT. [Internet] [Masters thesis]. Clemson University; 2011. [cited 2021 Jan 28]. Available from: https://tigerprints.clemson.edu/all_theses/1149.

Council of Science Editors:

Elraghy O. REPRESSION OF MULTIPLE CYP2D GENES IN MOUSE USING A SINGLE SIRNA CONSTRUCT. [Masters Thesis]. Clemson University; 2011. Available from: https://tigerprints.clemson.edu/all_theses/1149

14. Levinson, Nathanael Simeon. Towards the elucidation of the mechanism of the antibiotic activity of tamoxifen.

Degree: MS, Chemistry and Biochemistry, 2017, Georgia Tech

 Antibiotic resistance is increasingly a health and financial burden on the global population. Use and misuse of antibiotics has led to increased frequencies of antibiotic-resistant… (more)

Subjects/Keywords: Antibiotics; Tamoxifen

…Figure B9 – NMR of desmethyl tamoxifen 69 Figure B10 – Mass spec of NL-I-43 70 Figure B11… …of tamoxifen in SA 79 Figure C2 – MIC of tamoxifen in MRSA 79 Figure C3 – MIC of… …desmethyl tamoxifen in SA 80 Figure C4 – MIC of desmethyl tamoxifen in MRSA 80 Figure C5 – MIC… …of didesmethyl tamoxifen in SA 81 Figure C6 – MIC of didesmethyl tamoxifen in MRSA 81… …Figure C23 – MIC of 4-hydroxy tamoxifen in SA 90 Figure C24 – MIC of 4-hydroxy tamoxifen in… 

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

APA (6th Edition):

Levinson, N. S. (2017). Towards the elucidation of the mechanism of the antibiotic activity of tamoxifen. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58251

Chicago Manual of Style (16th Edition):

Levinson, Nathanael Simeon. “Towards the elucidation of the mechanism of the antibiotic activity of tamoxifen.” 2017. Masters Thesis, Georgia Tech. Accessed January 28, 2021. http://hdl.handle.net/1853/58251.

MLA Handbook (7th Edition):

Levinson, Nathanael Simeon. “Towards the elucidation of the mechanism of the antibiotic activity of tamoxifen.” 2017. Web. 28 Jan 2021.

Vancouver:

Levinson NS. Towards the elucidation of the mechanism of the antibiotic activity of tamoxifen. [Internet] [Masters thesis]. Georgia Tech; 2017. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/1853/58251.

Council of Science Editors:

Levinson NS. Towards the elucidation of the mechanism of the antibiotic activity of tamoxifen. [Masters Thesis]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58251


University of Georgia

15. Rubin, Valeria Norma. Tamoxifen analogs bearing acidic-side chain substituents.

Degree: 2014, University of Georgia

 The estrogen receptor (ER) ligand 4-[1-(p-hydroxyphenyl)-2-phenylethyl]phenoxyacetic acid (HPPA) was previously found to have differential bone loss suppressive effects in the ovariectomized (OVX) rat approaching those… (more)

Subjects/Keywords: tamoxifen; SERMs; osteoporosis; raloxifene; estrogen replacement therapy

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APA (6th Edition):

Rubin, V. N. (2014). Tamoxifen analogs bearing acidic-side chain substituents. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/20248

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):

Rubin, Valeria Norma. “Tamoxifen analogs bearing acidic-side chain substituents.” 2014. Thesis, University of Georgia. Accessed January 28, 2021. http://hdl.handle.net/10724/20248.

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

MLA Handbook (7th Edition):

Rubin, Valeria Norma. “Tamoxifen analogs bearing acidic-side chain substituents.” 2014. Web. 28 Jan 2021.

Vancouver:

Rubin VN. Tamoxifen analogs bearing acidic-side chain substituents. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/10724/20248.

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

Council of Science Editors:

Rubin VN. Tamoxifen analogs bearing acidic-side chain substituents. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/20248

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


University of Louisville

16. Manavalan, Tissa Thomas. Dysregulation of microRNA expression in acquired endocrine-resistant breast cancer.

Degree: PhD, 2012, University of Louisville

 MicroRNAs (miRNAs) regulate gene expression at the post-transcriptional level by repressing translation or stimulating mRNA degradation. In this study, I tested the hypothesis that miRNAs… (more)

Subjects/Keywords: Breast cancer; endocrine; microRNA; resistance; Tamoxifen

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APA (6th Edition):

Manavalan, T. T. (2012). Dysregulation of microRNA expression in acquired endocrine-resistant breast cancer. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/897 ; https://ir.library.louisville.edu/etd/897

Chicago Manual of Style (16th Edition):

Manavalan, Tissa Thomas. “Dysregulation of microRNA expression in acquired endocrine-resistant breast cancer.” 2012. Doctoral Dissertation, University of Louisville. Accessed January 28, 2021. 10.18297/etd/897 ; https://ir.library.louisville.edu/etd/897.

MLA Handbook (7th Edition):

Manavalan, Tissa Thomas. “Dysregulation of microRNA expression in acquired endocrine-resistant breast cancer.” 2012. Web. 28 Jan 2021.

Vancouver:

Manavalan TT. Dysregulation of microRNA expression in acquired endocrine-resistant breast cancer. [Internet] [Doctoral dissertation]. University of Louisville; 2012. [cited 2021 Jan 28]. Available from: 10.18297/etd/897 ; https://ir.library.louisville.edu/etd/897.

Council of Science Editors:

Manavalan TT. Dysregulation of microRNA expression in acquired endocrine-resistant breast cancer. [Doctoral Dissertation]. University of Louisville; 2012. Available from: 10.18297/etd/897 ; https://ir.library.louisville.edu/etd/897


University of Sydney

17. Stuart, Kirsten Elizabeth. Optimising the management of ductal carcinoma in situ of the breast: diagnosis, treatment and outcomes .

Degree: 2014, University of Sydney

 Ductal carcinoma in situ (DCIS) of the breast is common, now representing one-fifth of breast cancers detected at breast-screening; the incidence increased dramatically two decades… (more)

Subjects/Keywords: DCIS; Surgery; Radiotherapy; Tamoxifen; Outcomes; Cardiac

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APA (6th Edition):

Stuart, K. E. (2014). Optimising the management of ductal carcinoma in situ of the breast: diagnosis, treatment and outcomes . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/13331

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):

Stuart, Kirsten Elizabeth. “Optimising the management of ductal carcinoma in situ of the breast: diagnosis, treatment and outcomes .” 2014. Thesis, University of Sydney. Accessed January 28, 2021. http://hdl.handle.net/2123/13331.

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

MLA Handbook (7th Edition):

Stuart, Kirsten Elizabeth. “Optimising the management of ductal carcinoma in situ of the breast: diagnosis, treatment and outcomes .” 2014. Web. 28 Jan 2021.

Vancouver:

Stuart KE. Optimising the management of ductal carcinoma in situ of the breast: diagnosis, treatment and outcomes . [Internet] [Thesis]. University of Sydney; 2014. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/2123/13331.

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

Council of Science Editors:

Stuart KE. Optimising the management of ductal carcinoma in situ of the breast: diagnosis, treatment and outcomes . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/13331

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

18. Orias, Frédéric. Contribution à l'évaluation des risques écotoxicologiques des effluents hospitaliers : bioconcentration, bioaccumulation et bioamplification des résidus pharmaceutiques : Contribution to ecotoxicological risk assessment of hospital effluents : bioconcentration, bioaccumulation and biomagnification of pharmaceutical compounds.

Degree: Docteur es, Environnement, 2015, Vaulx-en-Velin, Ecole nationale des travaux publics

Les hôpitaux génèrent des effluents riches en résidus pharmaceutiques (RP), fonctions de leurs activités de soins et de diagnostic. Certains de ces RP sont aujourd’hui… (more)

Subjects/Keywords: Effluents hospitaliers; Résidus pharmaceutiques; Bioconcentration; Bioaccumulation; Isotopes stables; Tamoxifen; Hospital effluents; Pharmaceutical compounds; Bioconcentration; Bioaccumulation; Stable isotopes; Tamoxifen

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

APA (6th Edition):

Orias, F. (2015). Contribution à l'évaluation des risques écotoxicologiques des effluents hospitaliers : bioconcentration, bioaccumulation et bioamplification des résidus pharmaceutiques : Contribution to ecotoxicological risk assessment of hospital effluents : bioconcentration, bioaccumulation and biomagnification of pharmaceutical compounds. (Doctoral Dissertation). Vaulx-en-Velin, Ecole nationale des travaux publics. Retrieved from http://www.theses.fr/2015ENTP0005

Chicago Manual of Style (16th Edition):

Orias, Frédéric. “Contribution à l'évaluation des risques écotoxicologiques des effluents hospitaliers : bioconcentration, bioaccumulation et bioamplification des résidus pharmaceutiques : Contribution to ecotoxicological risk assessment of hospital effluents : bioconcentration, bioaccumulation and biomagnification of pharmaceutical compounds.” 2015. Doctoral Dissertation, Vaulx-en-Velin, Ecole nationale des travaux publics. Accessed January 28, 2021. http://www.theses.fr/2015ENTP0005.

MLA Handbook (7th Edition):

Orias, Frédéric. “Contribution à l'évaluation des risques écotoxicologiques des effluents hospitaliers : bioconcentration, bioaccumulation et bioamplification des résidus pharmaceutiques : Contribution to ecotoxicological risk assessment of hospital effluents : bioconcentration, bioaccumulation and biomagnification of pharmaceutical compounds.” 2015. Web. 28 Jan 2021.

Vancouver:

Orias F. Contribution à l'évaluation des risques écotoxicologiques des effluents hospitaliers : bioconcentration, bioaccumulation et bioamplification des résidus pharmaceutiques : Contribution to ecotoxicological risk assessment of hospital effluents : bioconcentration, bioaccumulation and biomagnification of pharmaceutical compounds. [Internet] [Doctoral dissertation]. Vaulx-en-Velin, Ecole nationale des travaux publics; 2015. [cited 2021 Jan 28]. Available from: http://www.theses.fr/2015ENTP0005.

Council of Science Editors:

Orias F. Contribution à l'évaluation des risques écotoxicologiques des effluents hospitaliers : bioconcentration, bioaccumulation et bioamplification des résidus pharmaceutiques : Contribution to ecotoxicological risk assessment of hospital effluents : bioconcentration, bioaccumulation and biomagnification of pharmaceutical compounds. [Doctoral Dissertation]. Vaulx-en-Velin, Ecole nationale des travaux publics; 2015. Available from: http://www.theses.fr/2015ENTP0005


Ruhr Universität Bochum

19. Vanheiden, Svenja. Der spannungsabhängige offene Kanalblock der G-Protein-gekoppelten einwärtsgleichrichtenden Kaliumkanäle durchTamoxifen an atrialen Myozyten von Ratten.

Degree: 2014, Ruhr Universität Bochum

Tamoxifen ist ein selektiver Östrogen-Antagonist und wird in der Therapie des hormonsensitiven Mammakarzinoms eingesetzt. In dieser Arbeit wurden die Effekte von Tamoxifen am G-Proteingekoppelten einwärtsgleichrichtenden… (more)

Subjects/Keywords: Tamoxifen; Kaliumkanal; GTP-bindende Proteine; Brustkrebs; Patch-Clamp-Methode

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APA (6th Edition):

Vanheiden, S. (2014). Der spannungsabhängige offene Kanalblock der G-Protein-gekoppelten einwärtsgleichrichtenden Kaliumkanäle durchTamoxifen an atrialen Myozyten von Ratten. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-43308

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):

Vanheiden, Svenja. “Der spannungsabhängige offene Kanalblock der G-Protein-gekoppelten einwärtsgleichrichtenden Kaliumkanäle durchTamoxifen an atrialen Myozyten von Ratten.” 2014. Thesis, Ruhr Universität Bochum. Accessed January 28, 2021. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-43308.

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

MLA Handbook (7th Edition):

Vanheiden, Svenja. “Der spannungsabhängige offene Kanalblock der G-Protein-gekoppelten einwärtsgleichrichtenden Kaliumkanäle durchTamoxifen an atrialen Myozyten von Ratten.” 2014. Web. 28 Jan 2021.

Vancouver:

Vanheiden S. Der spannungsabhängige offene Kanalblock der G-Protein-gekoppelten einwärtsgleichrichtenden Kaliumkanäle durchTamoxifen an atrialen Myozyten von Ratten. [Internet] [Thesis]. Ruhr Universität Bochum; 2014. [cited 2021 Jan 28]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-43308.

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

Council of Science Editors:

Vanheiden S. Der spannungsabhängige offene Kanalblock der G-Protein-gekoppelten einwärtsgleichrichtenden Kaliumkanäle durchTamoxifen an atrialen Myozyten von Ratten. [Thesis]. Ruhr Universität Bochum; 2014. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-43308

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


Universidade do Rio Grande do Norte

20. Jatobá, Carlos André Nunes. Avaliação bioquímica e hostológica de fígado de ratas wistar diabéticas e tratadas com tamoxifeno .

Degree: 2007, Universidade do Rio Grande do Norte

Tamoxifen (TX), a drug used in the treatment of breast cancer, may cause hepatic changes in some patients. The consequences of its use on the… (more)

Subjects/Keywords: Fígado; Hemossiderina; Siderose; Ferro; Tamoxifeno; Liver; Hemosiderin; Siderosis; Iron overload; Tamoxifen

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APA (6th Edition):

Jatobá, C. A. N. (2007). Avaliação bioquímica e hostológica de fígado de ratas wistar diabéticas e tratadas com tamoxifeno . (Thesis). Universidade do Rio Grande do Norte. Retrieved from http://repositorio.ufrn.br/handle/123456789/13111

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):

Jatobá, Carlos André Nunes. “Avaliação bioquímica e hostológica de fígado de ratas wistar diabéticas e tratadas com tamoxifeno .” 2007. Thesis, Universidade do Rio Grande do Norte. Accessed January 28, 2021. http://repositorio.ufrn.br/handle/123456789/13111.

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

MLA Handbook (7th Edition):

Jatobá, Carlos André Nunes. “Avaliação bioquímica e hostológica de fígado de ratas wistar diabéticas e tratadas com tamoxifeno .” 2007. Web. 28 Jan 2021.

Vancouver:

Jatobá CAN. Avaliação bioquímica e hostológica de fígado de ratas wistar diabéticas e tratadas com tamoxifeno . [Internet] [Thesis]. Universidade do Rio Grande do Norte; 2007. [cited 2021 Jan 28]. Available from: http://repositorio.ufrn.br/handle/123456789/13111.

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

Council of Science Editors:

Jatobá CAN. Avaliação bioquímica e hostológica de fígado de ratas wistar diabéticas e tratadas com tamoxifeno . [Thesis]. Universidade do Rio Grande do Norte; 2007. Available from: http://repositorio.ufrn.br/handle/123456789/13111

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


Penn State University

21. Blevins Primeau, Andrea Sascha. UDP-glucuronosyltransferase 2B7 glucuronidation of the active tamoxifen metabolites .

Degree: 2011, Penn State University

Tamoxifen (TAM) is a non-steroidal selective estrogen receptor modulator that was approved by the FDA in 1977 for the treatment of breast cancer. Although it… (more)

Subjects/Keywords: pharmacogenetics; drug metabolism; breast cancer; Src; tamoxifen; UGT; polymorphisms

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APA (6th Edition):

Blevins Primeau, A. S. (2011). UDP-glucuronosyltransferase 2B7 glucuronidation of the active tamoxifen metabolites . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12439

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):

Blevins Primeau, Andrea Sascha. “UDP-glucuronosyltransferase 2B7 glucuronidation of the active tamoxifen metabolites .” 2011. Thesis, Penn State University. Accessed January 28, 2021. https://submit-etda.libraries.psu.edu/catalog/12439.

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

MLA Handbook (7th Edition):

Blevins Primeau, Andrea Sascha. “UDP-glucuronosyltransferase 2B7 glucuronidation of the active tamoxifen metabolites .” 2011. Web. 28 Jan 2021.

Vancouver:

Blevins Primeau AS. UDP-glucuronosyltransferase 2B7 glucuronidation of the active tamoxifen metabolites . [Internet] [Thesis]. Penn State University; 2011. [cited 2021 Jan 28]. Available from: https://submit-etda.libraries.psu.edu/catalog/12439.

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

Council of Science Editors:

Blevins Primeau AS. UDP-glucuronosyltransferase 2B7 glucuronidation of the active tamoxifen metabolites . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/12439

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


Queens University

22. Sellars, Erin. Glucocorticoid Receptor Function and its Role in Tamoxifen Resistance .

Degree: Biochemistry, 2015, Queens University

 The function of the glucocorticoid receptor (GR) is crucial for the development and proliferation of normal human breast cells. The primary activity of GR is… (more)

Subjects/Keywords: Breast Cancer ; Tamoxifen Resistance ; Estrogen Receptor ; Glucocorticoid Receptor

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APA (6th Edition):

Sellars, E. (2015). Glucocorticoid Receptor Function and its Role in Tamoxifen Resistance . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13692

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):

Sellars, Erin. “Glucocorticoid Receptor Function and its Role in Tamoxifen Resistance .” 2015. Thesis, Queens University. Accessed January 28, 2021. http://hdl.handle.net/1974/13692.

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

MLA Handbook (7th Edition):

Sellars, Erin. “Glucocorticoid Receptor Function and its Role in Tamoxifen Resistance .” 2015. Web. 28 Jan 2021.

Vancouver:

Sellars E. Glucocorticoid Receptor Function and its Role in Tamoxifen Resistance . [Internet] [Thesis]. Queens University; 2015. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/1974/13692.

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

Council of Science Editors:

Sellars E. Glucocorticoid Receptor Function and its Role in Tamoxifen Resistance . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13692

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


University of Toronto

23. Gupta, Rashi. Tamoxifen Inhibits ERα Positive Breast Cancer Progression by Disrupting the ERα-JMJD2B Signaling Axis.

Degree: 2015, University of Toronto

JMJD2B is a histone demethylase for H3K9me3. Our lab has shown that JMJD2B is a co-factor of estrogen receptor in breast cancer proliferation: JMJD2B knockdown… (more)

Subjects/Keywords: Breast Cancer; Estrogen receptor; histone demethylation; JMJD2B; Tamoxifen; 0379

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APA (6th Edition):

Gupta, R. (2015). Tamoxifen Inhibits ERα Positive Breast Cancer Progression by Disrupting the ERα-JMJD2B Signaling Axis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/69638

Chicago Manual of Style (16th Edition):

Gupta, Rashi. “Tamoxifen Inhibits ERα Positive Breast Cancer Progression by Disrupting the ERα-JMJD2B Signaling Axis.” 2015. Masters Thesis, University of Toronto. Accessed January 28, 2021. http://hdl.handle.net/1807/69638.

MLA Handbook (7th Edition):

Gupta, Rashi. “Tamoxifen Inhibits ERα Positive Breast Cancer Progression by Disrupting the ERα-JMJD2B Signaling Axis.” 2015. Web. 28 Jan 2021.

Vancouver:

Gupta R. Tamoxifen Inhibits ERα Positive Breast Cancer Progression by Disrupting the ERα-JMJD2B Signaling Axis. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/1807/69638.

Council of Science Editors:

Gupta R. Tamoxifen Inhibits ERα Positive Breast Cancer Progression by Disrupting the ERα-JMJD2B Signaling Axis. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69638


Wayne State University

24. Haagenson, Kelly. Expression And Regulation Of Map Kinase Phosphatases 1 And 2 In Breast Cancer Tamoxifen Sensitivity.

Degree: PhD, Cancer Biology, 2013, Wayne State University

  ABSTRACT EXPRESSION AND REGULATION OF MAP KINASE PHOSPHATASES 1 and 2 IN BREAST CANCER TAMOXIFEN SENSITIVITY by KELLY K. HAAGENSON May 2013 Advisor: Dr.… (more)

Subjects/Keywords: Breast Cancer; MAP Kinase Phosphatases; Tamoxifen Sensitivity; Biology; Oncology

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

APA (6th Edition):

Haagenson, K. (2013). Expression And Regulation Of Map Kinase Phosphatases 1 And 2 In Breast Cancer Tamoxifen Sensitivity. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/659

Chicago Manual of Style (16th Edition):

Haagenson, Kelly. “Expression And Regulation Of Map Kinase Phosphatases 1 And 2 In Breast Cancer Tamoxifen Sensitivity.” 2013. Doctoral Dissertation, Wayne State University. Accessed January 28, 2021. https://digitalcommons.wayne.edu/oa_dissertations/659.

MLA Handbook (7th Edition):

Haagenson, Kelly. “Expression And Regulation Of Map Kinase Phosphatases 1 And 2 In Breast Cancer Tamoxifen Sensitivity.” 2013. Web. 28 Jan 2021.

Vancouver:

Haagenson K. Expression And Regulation Of Map Kinase Phosphatases 1 And 2 In Breast Cancer Tamoxifen Sensitivity. [Internet] [Doctoral dissertation]. Wayne State University; 2013. [cited 2021 Jan 28]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/659.

Council of Science Editors:

Haagenson K. Expression And Regulation Of Map Kinase Phosphatases 1 And 2 In Breast Cancer Tamoxifen Sensitivity. [Doctoral Dissertation]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_dissertations/659


Washington State University

25. [No author]. OVARIAN PHYSIOLOGY IN A NON-DOMESTICATED BIRD: MECHANISMS BEHIND THE ACCUMULATION AND VARIATION OF YOLK ANDROGENS IN HOUSE SPARROWS .

Degree: 2011, Washington State University

 In birds and other oviparous species, the accumulation of maternally-derived yolk androgens may represent an adaptive transgenerational information system. Researchers have found multiple effects of… (more)

Subjects/Keywords: GnRH; House sparrows; Maternal effects; Steroidogenic enzymes; Tamoxifen; Yolk androgens

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

APA (6th Edition):

author], [. (2011). OVARIAN PHYSIOLOGY IN A NON-DOMESTICATED BIRD: MECHANISMS BEHIND THE ACCUMULATION AND VARIATION OF YOLK ANDROGENS IN HOUSE SPARROWS . (Thesis). Washington State University. Retrieved from http://hdl.handle.net/2376/2919

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):

author], [No. “OVARIAN PHYSIOLOGY IN A NON-DOMESTICATED BIRD: MECHANISMS BEHIND THE ACCUMULATION AND VARIATION OF YOLK ANDROGENS IN HOUSE SPARROWS .” 2011. Thesis, Washington State University. Accessed January 28, 2021. http://hdl.handle.net/2376/2919.

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

MLA Handbook (7th Edition):

author], [No. “OVARIAN PHYSIOLOGY IN A NON-DOMESTICATED BIRD: MECHANISMS BEHIND THE ACCUMULATION AND VARIATION OF YOLK ANDROGENS IN HOUSE SPARROWS .” 2011. Web. 28 Jan 2021.

Vancouver:

author] [. OVARIAN PHYSIOLOGY IN A NON-DOMESTICATED BIRD: MECHANISMS BEHIND THE ACCUMULATION AND VARIATION OF YOLK ANDROGENS IN HOUSE SPARROWS . [Internet] [Thesis]. Washington State University; 2011. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/2376/2919.

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

Council of Science Editors:

author] [. OVARIAN PHYSIOLOGY IN A NON-DOMESTICATED BIRD: MECHANISMS BEHIND THE ACCUMULATION AND VARIATION OF YOLK ANDROGENS IN HOUSE SPARROWS . [Thesis]. Washington State University; 2011. Available from: http://hdl.handle.net/2376/2919

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


University of Illinois – Chicago

26. Patel, Hitisha K. Novel Approaches to Endocrine Therapy in Endocrine-Independent Breast Cancer.

Degree: 2016, University of Illinois – Chicago

Tamoxifen, an antagonist at estrogen receptor alpha (ERα) in breast tissue, and the prototypical selective estrogen receptor modulator (SERM), is the standard of care for… (more)

Subjects/Keywords: Breast cancer; estrogen receptor; tamoxifen resistance; partial agonists; therapeutics

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

APA (6th Edition):

Patel, H. K. (2016). Novel Approaches to Endocrine Therapy in Endocrine-Independent Breast Cancer. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/20928

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):

Patel, Hitisha K. “Novel Approaches to Endocrine Therapy in Endocrine-Independent Breast Cancer.” 2016. Thesis, University of Illinois – Chicago. Accessed January 28, 2021. http://hdl.handle.net/10027/20928.

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

MLA Handbook (7th Edition):

Patel, Hitisha K. “Novel Approaches to Endocrine Therapy in Endocrine-Independent Breast Cancer.” 2016. Web. 28 Jan 2021.

Vancouver:

Patel HK. Novel Approaches to Endocrine Therapy in Endocrine-Independent Breast Cancer. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2021 Jan 28]. Available from: http://hdl.handle.net/10027/20928.

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

Council of Science Editors:

Patel HK. Novel Approaches to Endocrine Therapy in Endocrine-Independent Breast Cancer. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/20928

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


University of Manchester

27. O'Brien, Ciara. Breast Cancer Initiating Cells in Tamoxifen Treatment and Resistance.

Degree: 2012, University of Manchester

 Resistance to endocrine treatments in oestrogen receptor positive (ER+) breast cancer (BC) significantly contribute to patient morbidity and mortality. ER+ BC constitute 60% of all… (more)

Subjects/Keywords: breast cancer; tamoxifen; stem cell; treatment resistance; xenograft; oestrogen receptor

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

APA (6th Edition):

O'Brien, C. (2012). Breast Cancer Initiating Cells in Tamoxifen Treatment and Resistance. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162494

Chicago Manual of Style (16th Edition):

O'Brien, Ciara. “Breast Cancer Initiating Cells in Tamoxifen Treatment and Resistance.” 2012. Doctoral Dissertation, University of Manchester. Accessed January 28, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162494.

MLA Handbook (7th Edition):

O'Brien, Ciara. “Breast Cancer Initiating Cells in Tamoxifen Treatment and Resistance.” 2012. Web. 28 Jan 2021.

Vancouver:

O'Brien C. Breast Cancer Initiating Cells in Tamoxifen Treatment and Resistance. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Jan 28]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162494.

Council of Science Editors:

O'Brien C. Breast Cancer Initiating Cells in Tamoxifen Treatment and Resistance. [Doctoral Dissertation]. University of Manchester; 2012. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:162494

28. Abu Rabi Zaki. Significance of biological heterogeneity of breast carcinomas in response to antiestrogen therapy.

Degree: PhD, Biology, 2010, University of Belgrade

Analysis of biological heterogeneity of estrogen-dependant primary operable breast cancer in postmenopausal patients treated with tamoxifen, had, as а goal, analysis of its significance in… (more)

Subjects/Keywords: breast cancer; tamoxifen; resistance; kancer dojke; tamoksifen; rezistencija

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

APA (6th Edition):

Zaki, A. R. (2010). Significance of biological heterogeneity of breast carcinomas in response to antiestrogen therapy. (Doctoral Dissertation). University of Belgrade. Retrieved from http://dx.doi.org/10.2298/BG20100618ABURABI ; http://eteze.bg.ac.rs/application/showtheses?thesesId=594 ; https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024545458

Chicago Manual of Style (16th Edition):

Zaki, Abu Rabi. “Significance of biological heterogeneity of breast carcinomas in response to antiestrogen therapy.” 2010. Doctoral Dissertation, University of Belgrade. Accessed January 28, 2021. http://dx.doi.org/10.2298/BG20100618ABURABI ; http://eteze.bg.ac.rs/application/showtheses?thesesId=594 ; https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024545458.

MLA Handbook (7th Edition):

Zaki, Abu Rabi. “Significance of biological heterogeneity of breast carcinomas in response to antiestrogen therapy.” 2010. Web. 28 Jan 2021.

Vancouver:

Zaki AR. Significance of biological heterogeneity of breast carcinomas in response to antiestrogen therapy. [Internet] [Doctoral dissertation]. University of Belgrade; 2010. [cited 2021 Jan 28]. Available from: http://dx.doi.org/10.2298/BG20100618ABURABI ; http://eteze.bg.ac.rs/application/showtheses?thesesId=594 ; https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024545458.

Council of Science Editors:

Zaki AR. Significance of biological heterogeneity of breast carcinomas in response to antiestrogen therapy. [Doctoral Dissertation]. University of Belgrade; 2010. Available from: http://dx.doi.org/10.2298/BG20100618ABURABI ; http://eteze.bg.ac.rs/application/showtheses?thesesId=594 ; https://fedorabg.bg.ac.rs/fedora/get/o:6759/bdef:Content/get ; http://vbs.rs/scripts/cobiss?command=SEARCH&base=99999&select=ID=1024545458


University of California – San Francisco

29. Tchu, Simone Ming. Tamoxifen Pharmacogenetics: CYP2D6 and Other Variables Influencing Tamoxifen and Tamoxifen Metabolite Exposure.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2013, University of California – San Francisco

Tamoxifen is a selective estrogen receptor modulator (SERM) that is used for the treatment of estrogen receptor positive (ER+) breast cancer, most commonly as an… (more)

Subjects/Keywords: Pharmaceutical sciences; Genetics; Breast Cancer; CYP2D6; Endoxifen; Pharmacogenetics; Tamoxifen

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

APA (6th Edition):

Tchu, S. M. (2013). Tamoxifen Pharmacogenetics: CYP2D6 and Other Variables Influencing Tamoxifen and Tamoxifen Metabolite Exposure. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/96r0s5cw

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):

Tchu, Simone Ming. “Tamoxifen Pharmacogenetics: CYP2D6 and Other Variables Influencing Tamoxifen and Tamoxifen Metabolite Exposure.” 2013. Thesis, University of California – San Francisco. Accessed January 28, 2021. http://www.escholarship.org/uc/item/96r0s5cw.

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

MLA Handbook (7th Edition):

Tchu, Simone Ming. “Tamoxifen Pharmacogenetics: CYP2D6 and Other Variables Influencing Tamoxifen and Tamoxifen Metabolite Exposure.” 2013. Web. 28 Jan 2021.

Vancouver:

Tchu SM. Tamoxifen Pharmacogenetics: CYP2D6 and Other Variables Influencing Tamoxifen and Tamoxifen Metabolite Exposure. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2021 Jan 28]. Available from: http://www.escholarship.org/uc/item/96r0s5cw.

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

Council of Science Editors:

Tchu SM. Tamoxifen Pharmacogenetics: CYP2D6 and Other Variables Influencing Tamoxifen and Tamoxifen Metabolite Exposure. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/96r0s5cw

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


University of Manchester

30. Azadbakht, Narges. Stromal and epithelial changes in breast cancer following endocrine treatment.

Degree: PhD, 2014, University of Manchester

 Anti-oestrogens and aromatase inhibitors are currently used as endocrine therapies in breast cancer. Despite the significant role that these treatments play in reducing breast cancer… (more)

Subjects/Keywords: 616.99; Breast cancer; endocrine treatment; tamoxifen; Systems biology

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

APA (6th Edition):

Azadbakht, N. (2014). Stromal and epithelial changes in breast cancer following endocrine treatment. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/stromal-and-epithelial-changes-in-breast-cancer-following-endocrine-treatment(c6542eba-83e2-48de-a566-8f5eccd9a7b1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632243

Chicago Manual of Style (16th Edition):

Azadbakht, Narges. “Stromal and epithelial changes in breast cancer following endocrine treatment.” 2014. Doctoral Dissertation, University of Manchester. Accessed January 28, 2021. https://www.research.manchester.ac.uk/portal/en/theses/stromal-and-epithelial-changes-in-breast-cancer-following-endocrine-treatment(c6542eba-83e2-48de-a566-8f5eccd9a7b1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632243.

MLA Handbook (7th Edition):

Azadbakht, Narges. “Stromal and epithelial changes in breast cancer following endocrine treatment.” 2014. Web. 28 Jan 2021.

Vancouver:

Azadbakht N. Stromal and epithelial changes in breast cancer following endocrine treatment. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2021 Jan 28]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/stromal-and-epithelial-changes-in-breast-cancer-following-endocrine-treatment(c6542eba-83e2-48de-a566-8f5eccd9a7b1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632243.

Council of Science Editors:

Azadbakht N. Stromal and epithelial changes in breast cancer following endocrine treatment. [Doctoral Dissertation]. University of Manchester; 2014. Available from: https://www.research.manchester.ac.uk/portal/en/theses/stromal-and-epithelial-changes-in-breast-cancer-following-endocrine-treatment(c6542eba-83e2-48de-a566-8f5eccd9a7b1).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.632243

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