Rozprawy doktorskie na temat „Estrogen”
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Järvenpää, Paula. "Intestinal metabolism of estrogens including some studies on medroxiprogesterone acetate and megestrol acetate". Helsinki : Finnish Society of Sciences and Letters, 1991. http://books.google.com/books?id=ee5qAAAAMAAJ.
Pełny tekst źródłaWade, Christian Bernard. "Mechanisms of estrogen rapid signaling /". Thesis, Connect to this title online; UW restricted, 2002. http://hdl.handle.net/1773/6272.
Pełny tekst źródłaNilsson, Ola. "The role of estrogen in growth plate chondrogenesis /". Stockholm, 2002. http://diss.kib.ki.se/2002/91-7349-410-0/.
Pełny tekst źródłaLee, Isaish Chi Kin. "Measuring the binding kinetics of estrogen receptor alpha and dietary estrogens". HKBU Institutional Repository, 2014. https://repository.hkbu.edu.hk/etd_oa/28.
Pełny tekst źródłaZhang, Qiu-Xia. "Estrogen receptor gene alterations in human breast cancer". Lund : Jubileumsinstitutionen, Dept. of Oncology,Lund University, 1997. http://catalog.hathitrust.org/api/volumes/oclc/39738537.html.
Pełny tekst źródłaScherr, Frank. "Sorption, degradation and transport of estrogens and estrogen sulphates in agricultural soils". Diss., Lincoln University, 2009. http://hdl.handle.net/10182/1017.
Pełny tekst źródłaGraham, Lisa Anne. "Environmental Estrogens: Assessing Human Gestational Exposure and Interactions with the Estrogen Receptor". Thesis, University of Canterbury. Chemistry, 2012. http://hdl.handle.net/10092/7173.
Pełny tekst źródłaLambert, K. Chad. "The effects of estrogen signaling in innate and adaptive immune cells /". Free to MU Campus, others may purchase, 2005. http://wwwlib.umi.com/cr/mo/fullcit?p3189934.
Pełny tekst źródłaAnsell, Peter James. "Regulation of the antioxidant response element by estrogens : a potential mechanism to help explain estrogen-induced cancer? /". free to MU campus, to others for purchase, 2004. http://wwwlib.umi.com/cr/mo/fullcit?p3137674.
Pełny tekst źródłaLinford, Nancy J. "Effects of estrogenic compounds on neuronal apoptotic pathways /". Thesis, Connect to this title online; UW restricted, 2001. http://hdl.handle.net/1773/6289.
Pełny tekst źródłaStewart, Ceri Elisabeth. "Estrogen receptor beta and estrogen response in breast cancer cell lines". Thesis, University of Liverpool, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491371.
Pełny tekst źródłaTanemura, Mai. "The role of estrogen and estrogen receptor β in choroidal neovascularization". Kyoto University, 2005. http://hdl.handle.net/2433/144767.
Pełny tekst źródłaPettersson, Katarina. "Signal transduction via estrogen receptors (ERs) and estrogen receptor-related receptors (ERRs) /". Stockholm, 2000. http://diss.kib.ki.se/2000/91-628-4184-X/.
Pełny tekst źródłaLee, Chun-lun. "Actions of estrogen and estrogen-related compounds on prostate cancer cell growth /". View the Table of Contents & Abstract, 2007. http://sunzi.lib.hku.hk/hkuto/record/B38297061.
Pełny tekst źródłaLee, Chun-lun, i 李振倫. "Actions of estrogen and estrogen-related compounds on prostate cancer cell growth". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2007. http://hub.hku.hk/bib/B45011266.
Pełny tekst źródłaLee, Annie S. (Annie Sang) 1975. "Molecular mechanism of interactions between estrogen receptor and estrogen receptor selective genotoxins". Thesis, Massachusetts Institute of Technology, 2000. http://hdl.handle.net/1721.1/73348.
Pełny tekst źródłaIncludes bibliographical references (leaves 43-47).
Although one million new breast cancer cases arise each year worldwide, therapies to treat the disease are limited. Conventional treatments including the chemotherapeutic agent, Tamoxifen, have had only limited success, often showing uncomfortable side effects. Our group has proposed a new scheme for a rational drug design. This scheme utilizes recent findings on the mechanism of cisplatin, the drug found to cure in excess of 93% of all testicular cancer cases. Cisplatin forms DNA adducts that are toxic. The toxicity of these adducts is enhanced by the recruitment of proteins that bind to the adducts and impede adduct repair. This thesis was an attempt to duplicate this "repair shielding" mechanism with another cytotoxin. Specifically, this toxin will be programmed to kill breast cancer cells. Breast cancer cells often overexpress the estrogen receptor protein. By synthesizing a drug that not only binds and damages the DNA but also binds the abundant proteins in the cells, thereby blocking the damaged site from DNA repair proteins, a selective treatment of cancer cells can be achieved. In this study, the human estrogen receptor (hER) and the ligand binding domain of the hER genes were cloned into baculovirus expression vectors, establishing a system where a large quantity of the proteins can be expressed. The proteins expressed in insect cells were purified in one step, using the FLAG-epitope, yielding homogeneous proteins. The proteins were tested for binding to p-estradiol and were confirmed to be functional in ligand binding. They were also tested for their ability to bind the novel drugs synthesized to bind both the protein and the DNA. It was found that the ligand binding domain of the hER was capable of binding the drugs adducted to the DNA. In an effort to elucidate the mechanism of the protein-drug-DNA complex formation, an association experiment was carried out, which showed that the drug more readily bound to the protein than to DNA. However, a significant amount of the drug-protein complex still bound the DNA, if the ratio of the protein to the drug did not exceed 1.5.
by Annie S. Lee.
S.M.
Karolczak, Magdalena. "Estrogen synthesis and novel mechanisms of estrogen action in the developing brain". Ulm : Universität Ulm, Medizinische Fakultät, 2000. http://www.bsz-bw.de/cgi-bin/xvms.cgi?SWB9394023.
Pełny tekst źródłaLi, Xiangrong. "Hormonal activation of genes through nongenomic pathways by estrogen and structurally diverse estrogenic compounds". Diss., Texas A&M University, 2006. http://hdl.handle.net/1969.1/3839.
Pełny tekst źródłaAndersson, Therése. "Estrogen and Glucocorticoid Metabolism". Doctoral thesis, Umeå universitet, Medicin, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-33165.
Pełny tekst źródłaLjunggren, Ribom Eva. "Muscles, Estrogen, and Bone". Doctoral thesis, Uppsala : Acta Universitatis Upsaliensis : Univ.-bibl. [distributör], 2003. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3779.
Pełny tekst źródłaHarrell, Joshua C. "Dissecting roles of estrogen receptors in breast cancer lymphatic metastasis /". Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2007.
Znajdź pełny tekst źródłaTypescript. Includes bibliographical references (leaves 125-140). Free to UCD affiliates. Online version available via ProQuest Digital Dissertations;
Brown, Greta Suzanne. "The Effects of Estrogen on the Growth and Tuberization of Potato Plants (Solanum tuberosum cv. 'Iwa') Grown in Liquid Tissue Culture Media". Thesis, University of Canterbury. Biological Sciences, 2006. http://hdl.handle.net/10092/1376.
Pełny tekst źródłaKarolczak, Magdalena [Verfasser]. "Estrogen synthesis and novel mechanisms of estrogen action in the developing brain / Magdalena Karolczak". Ulm : Universität Ulm. Medizinische Fakultät, 2001. http://d-nb.info/1015473156/34.
Pełny tekst źródłaCurran, Edward M. "Regulation of the estrogen receptor in human breast cancer cells /". free to MU campus, to others for purchase, 1998. http://wwwlib.umi.com/cr/mo/fullcit?p9901231.
Pełny tekst źródłaIslander, Ulrika. "Immunomodulation by estrogen and estren /". Göteborg : Department of Rheumatology and Inflammation Research, The Sahlgrenska Academy at Göteborg University, 2007. http://hdl.handle.net/2077/3123.
Pełny tekst źródłaCouse, John Floyd. "THE ROLE OF ESTROGEN RECEPTOR-a AND ESTROGEN RECEPTOR-b IN THE HYPERLUTEINIZED MOUSE OVARY". NCSU, 2004. http://www.lib.ncsu.edu/theses/available/etd-05212004-123339/.
Pełny tekst źródłaRussell, Nancy. "Estrogen Receptor Alpha in the Medial Preopic Area Mediates Male Rat Sexual Responses to Estrogen". Digital Archive @ GSU, 2010. http://digitalarchive.gsu.edu/biology_theses/25.
Pełny tekst źródłaShen, Minqian. "Roles of estrogen hormones and estrogen receptors on regulation of liver and liver cancer metabolism". Miami University / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=miami1492612390075921.
Pełny tekst źródłaZushin, Peter-James H. "The selective effect of estrogen receptor alpha and beta on activity and social behavior in neonatal male praire voles". Akron, OH : University of Akron, 2009. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=akron1248102221.
Pełny tekst źródła"August, 2009." Title from electronic thesis title page (viewed 10/7/2009) Advisor, Bruce Cushing; Committee members, Qin Liu, Todd Blackledge; Department Chair, Monte Turner; Dean of the College, Chand Midha; Dean of the Graduate School, George R. Newkome. Includes bibliographical references.
Philips, Brian John. "Protein interactions with the catechol estrogens 4-hydroxyestrone and 4-hydroxyestradiol in mouse tissue lysate : binding and metabolism studies /". free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3036851.
Pełny tekst źródłaCox, Brian Joseph. "Development of an assay for estrogenic endocrine disrupters involving the rat liver estrogen receptor alpha". Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk2/ftp01/MQ31820.pdf.
Pełny tekst źródłaGreiwe, Kelly. "Effects of estrogen on aggressive behavior". Connect to resource, 2006. http://hdl.handle.net/1811/6576.
Pełny tekst źródłaTitle from first page of PDF file. Document formatted into pages: contains 18 p.; also includes graphics. Includes bibliographical references (p. 16-18) Available online via Ohio State University's Knowledge Bank.
Mhyre, Andrew James. "Mechanisms of estrogen signaling in astrocytes /". Thesis, Connect to this title online; UW restricted, 2005. http://hdl.handle.net/1773/6266.
Pełny tekst źródłaRafi, Ali. "Estrogen action in growth plate cartilage". Thesis, Högskolan i Skövde, Institutionen för vård och natur, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-5463.
Pełny tekst źródłaHeldring, Nina. "Molecular basis of estrogen receptor antagonism /". Stockholm, 2006. http://diss.kib.ki.se/2006/91-7140-634-4/.
Pełny tekst źródłaPark, Se Hyung. "Estrogen in ovarian cancer cell metastasis". Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/1287.
Pełny tekst źródłaEng, Frank Chung Sing 1972. "Molecular mechanisms of estrogen receptor signaling". Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=38483.
Pełny tekst źródłaActivation of transcription by the ER requires the recruitment of different classes of coactivators. L536P interacted with coactivators in the absence of hormone and this constitutive interaction can be abolished by antiestrogens. We conclude that constitutive activity of L536P-HEGO is manifested to in part from constitutive coactivator binding. We also demonstrated that different classes of coactivators do not recognize the ER LBD in the same manner and can compete for binding to the ER LBD suggesting that different classes of coactivators recognize distinct but overlapping binding sites. Interestingly, coexpression of RIP140 blocked enhanced transactivation by HEGO observed in the presence of TIF-2, suggesting that RIP140 may play a negative role in ER signaling.
Using a yeast two-hybrid system with the ER LBD as bait, we isolated a novel estrogen receptor cofactor (ERC) that interacts with the ER LBD in a hormone dependent manner. The primary structure of ERC consists of 4 ankyrin repeat domains, 2 LXXLL motifs and an ATP/GTP binding domain. ERC is highly expressed in ovary, testes, and spleen, with moderate levels in heart, brain, and placenta. ERC repressed ER transactivation in several cell lines in the presence of estradiol suggesting that ERC may function as a novel estrogen dependent repressor of the ER. Immunohistochemistry and confocal microscopy localized ERC to the cytoplasm with partial nuclear staining. Recently, synphilin-1, a novel protein that has been implicated in the pathogenesis of Parkinson's disease was isolated and is identical to ERC. A role for ERC in intracellular signaling through a membrane bound ER in the brain is currently being investigated.
Nelson, Adam William. "Estrogen receptor beta modulates prostate carcinogenesis". Thesis, University of Cambridge, 2017. https://www.repository.cam.ac.uk/handle/1810/267736.
Pełny tekst źródłaZilmer, Johansen Anne Katrine. "Estrogen metabolism in pulmonary arterial hypertension". Thesis, University of Glasgow, 2014. http://theses.gla.ac.uk/5199/.
Pełny tekst źródłaMobley, James Austin. "Oxidative mechanisms of estrogen induced carcinogenesis /". The Ohio State University, 2000. http://rave.ohiolink.edu/etdc/view?acc_num=osu148819623490807.
Pełny tekst źródłaSinger, Cherie A. "Neurotrophic and neuroprotective effects of estrogen /". Thesis, Connect to this title online; UW restricted, 1998. http://hdl.handle.net/1773/6301.
Pełny tekst źródłaJain, Disha. "New approaches to estrogen receptor modulation". Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 157 p, 2009. http://proquest.umi.com/pqdweb?did=1818417411&sid=4&Fmt=2&clientId=8331&RQT=309&VName=PQD.
Pełny tekst źródłaForyst-Ludwig, Anna [Verfasser]. "Obesity-related cardiovascular and metabolic diseases : the role of estrogens, estrogen receptors and PPARgamma / Anna Foryst-Ludwig". Berlin : Medizinische Fakultät Charité - Universitätsmedizin Berlin, 2014. http://d-nb.info/1052530788/34.
Pełny tekst źródłaBjörnström, Linda. "Molecular mechanisms of alternative estrogen receptor signaling /". Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-509-3/.
Pełny tekst źródłaSusiarjo, Martha. "IDENTIFICATION AND CHARACTERIZATION OF ESTROGEN-MEDIATED EFFECTS ON FEMALE MEIOSIS: STUDIES OF BISPHENOL A AND ESTROGEN RECEPTORS". Connect to text online, 2007. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1158685403.
Pełny tekst źródłaTasci, Arzu Gul. "Biomechanical Evaluation Of Effects Of Estrogen, Selective Estrogen Receptor Modulator Drugs And Vitamin K2 On Osteoporotic Bone". Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/12605451/index.pdf.
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s were resulted in numerically (though not statistically significant) higher values on femur mechanical properties, and significantly better on tibia compared to the untreated controls. VitK2 performs well in energy absorption upto fracture, but worse in others (PL, YL etc.) compared to other treatments indicating that it plays a specific role in modifying bone structure thus, rendering bone stronger under high stress. However, similar to estrogen case, its combination with raloxifen performs better than its individual administration. With combinations it was aimed to reduce the adverse effects of estrogen on uterus and mammary glands by using raloxifen. This idea appears to be achieved with better histological results of uterus in combinations than estrogen groups. Additionally it was observed that direct strain data obtained by strain gauge experiments can be more informative than theoretical model in calculating modulus of elasticity, and shown that shear contribution can be neglected if depth/span ratio and set up dimensions properly chosen. Biochemical analysis of the blood showed an increment in bone formation (ALP activity) compared to both controls. ALP activity was the highest in R group, which was lower in combinations. Thus existence of a different mechanism in osteoporotic bone repair in combinations was suggested.
Brummer, Tyson Peter Thomas. "Comparative Immunological Effects of a Natural Estrogen (17β-estradiol) versus a Pharmacologic Synthetic Estrogen (17α-ethinyl estradiol)". Thesis, Virginia Tech, 2007. http://hdl.handle.net/10919/34601.
Pełny tekst źródłaMaster of Science
Lau, Kin-Mang. "Estrogen and Antiestrogen Actions on Human Prostate Cancer: A Dissertation". eScholarship@UMMS, 2001. https://escholarship.umassmed.edu/gsbs_diss/37.
Pełny tekst źródłaStavréus-Evers, Anneli. "Implantation : morphological and biochemical characterization of the receptive human endometrium /". Stockholm, 2002. http://diss.kib.ki.se/2002/91-7349-313-9.
Pełny tekst źródłaTrauernicht, Amy Michelle. "The role of the deleted in breast cancer 1 gene product, DBC-1, in estrogen-independent breast cancer cell survival : a dissertation /". San Antonio : UTHSC, 2007. http://proquest.umi.com/pqdweb?did=1407489201&sid=1&Fmt=2&clientId=70986&RQT=309&VName=PQD.
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