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You searched for subject:(Cyclooxygenase). Showing records 1 – 30 of 238 total matches.

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Vanderbilt University

1. Sprinkel, Katie Connors. Investigating the Biological Activity of the Novel Hemiketal Eicosanoid E2.

Degree: MS, Interdisciplinary Studies: Analytical Pharmacology, 2016, Vanderbilt University

 Eicosanoids, such as prostaglandins, leukotrienes, hydroxy- and epoxy-derivatives of arachidonic acid (AA), are lipid autacoids that regulate constitutive as well as inflammatory processes. Prostaglandins (PGs)… (more)

Subjects/Keywords: eicosanoid; cyclooxygenase 2

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APA (6th Edition):

Sprinkel, K. C. (2016). Investigating the Biological Activity of the Novel Hemiketal Eicosanoid E2. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11528

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):

Sprinkel, Katie Connors. “Investigating the Biological Activity of the Novel Hemiketal Eicosanoid E2.” 2016. Thesis, Vanderbilt University. Accessed April 18, 2021. http://hdl.handle.net/1803/11528.

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

MLA Handbook (7th Edition):

Sprinkel, Katie Connors. “Investigating the Biological Activity of the Novel Hemiketal Eicosanoid E2.” 2016. Web. 18 Apr 2021.

Vancouver:

Sprinkel KC. Investigating the Biological Activity of the Novel Hemiketal Eicosanoid E2. [Internet] [Thesis]. Vanderbilt University; 2016. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1803/11528.

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

Council of Science Editors:

Sprinkel KC. Investigating the Biological Activity of the Novel Hemiketal Eicosanoid E2. [Thesis]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/11528

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


Mississippi State University

2. Thomason, John Metcalfe. THE EFFECTS OF ASPIRIN AND CYCLOSPORINE ON CANINE PLATELET FUNCTION AND CYCLOOXYGENASE EXPRESSION.

Degree: MS, Department of Clinical Sciences, 2012, Mississippi State University

  Immune-mediated hemolytic anemia (IMHA) is one of the most common causes of anemia in dogs. Despite aggressive therapy, there is a 50% mortality rate… (more)

Subjects/Keywords: dog; cyclosporine; cyclooxygenase; aspirin; Platelets

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APA (6th Edition):

Thomason, J. M. (2012). THE EFFECTS OF ASPIRIN AND CYCLOSPORINE ON CANINE PLATELET FUNCTION AND CYCLOOXYGENASE EXPRESSION. (Masters Thesis). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-03192012-124504/ ;

Chicago Manual of Style (16th Edition):

Thomason, John Metcalfe. “THE EFFECTS OF ASPIRIN AND CYCLOSPORINE ON CANINE PLATELET FUNCTION AND CYCLOOXYGENASE EXPRESSION.” 2012. Masters Thesis, Mississippi State University. Accessed April 18, 2021. http://sun.library.msstate.edu/ETD-db/theses/available/etd-03192012-124504/ ;.

MLA Handbook (7th Edition):

Thomason, John Metcalfe. “THE EFFECTS OF ASPIRIN AND CYCLOSPORINE ON CANINE PLATELET FUNCTION AND CYCLOOXYGENASE EXPRESSION.” 2012. Web. 18 Apr 2021.

Vancouver:

Thomason JM. THE EFFECTS OF ASPIRIN AND CYCLOSPORINE ON CANINE PLATELET FUNCTION AND CYCLOOXYGENASE EXPRESSION. [Internet] [Masters thesis]. Mississippi State University; 2012. [cited 2021 Apr 18]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-03192012-124504/ ;.

Council of Science Editors:

Thomason JM. THE EFFECTS OF ASPIRIN AND CYCLOSPORINE ON CANINE PLATELET FUNCTION AND CYCLOOXYGENASE EXPRESSION. [Masters Thesis]. Mississippi State University; 2012. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-03192012-124504/ ;


Vanderbilt University

3. Goodman, Michael Christopher. Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis.

Degree: PhD, Chemistry, 2018, Vanderbilt University

 Polyunsaturated fatty acids can be liberated from phospholipids in the membrane bilayer and enzymatically converted to oxygenated bioactive lipid compounds that contribute to the pathology,… (more)

Subjects/Keywords: prostaglandins; cyclooxygenase; Inflammation; enzyme kinetics

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APA (6th Edition):

Goodman, M. C. (2018). Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10966

Chicago Manual of Style (16th Edition):

Goodman, Michael Christopher. “Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed April 18, 2021. http://hdl.handle.net/1803/10966.

MLA Handbook (7th Edition):

Goodman, Michael Christopher. “Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis.” 2018. Web. 18 Apr 2021.

Vancouver:

Goodman MC. Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1803/10966.

Council of Science Editors:

Goodman MC. Investigations of the enzymatic mechanisms and inhibition of prostaglandin E2 biosynthesis. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/10966


University of Rochester

4. Matousek, Sarah Bliss; O'Banion, M. Kerry. Chronic Neuroinflammation: Contribution of IL-1β to Prostaglandin Production and Alzheimer's Disease Pathology.

Degree: PhD, 2011, University of Rochester

 Interleukin-1β (IL-1β) is a pleiotropic cytokine capable of initiating and propagating brain neuroinflammatory responses to injury and infection. The role of IL-1 in acute inflammatory… (more)

Subjects/Keywords: Neuroinflammation; Alzheimer's Disease; Interleukin-1β; Prostaglandins; Cyclooxygenase-1; Cyclooxygenase-2

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APA (6th Edition):

Matousek, Sarah Bliss; O'Banion, M. K. (2011). Chronic Neuroinflammation: Contribution of IL-1β to Prostaglandin Production and Alzheimer's Disease Pathology. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/13948

Chicago Manual of Style (16th Edition):

Matousek, Sarah Bliss; O'Banion, M Kerry. “Chronic Neuroinflammation: Contribution of IL-1β to Prostaglandin Production and Alzheimer's Disease Pathology.” 2011. Doctoral Dissertation, University of Rochester. Accessed April 18, 2021. http://hdl.handle.net/1802/13948.

MLA Handbook (7th Edition):

Matousek, Sarah Bliss; O'Banion, M Kerry. “Chronic Neuroinflammation: Contribution of IL-1β to Prostaglandin Production and Alzheimer's Disease Pathology.” 2011. Web. 18 Apr 2021.

Vancouver:

Matousek, Sarah Bliss; O'Banion MK. Chronic Neuroinflammation: Contribution of IL-1β to Prostaglandin Production and Alzheimer's Disease Pathology. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1802/13948.

Council of Science Editors:

Matousek, Sarah Bliss; O'Banion MK. Chronic Neuroinflammation: Contribution of IL-1β to Prostaglandin Production and Alzheimer's Disease Pathology. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/13948


Brigham Young University

5. Xu, Yibing. Studies on Cyclooxygenase-1, its Structure and Splice Variants, and Modulation of Cyclooxygenase-2 by Inducible Nitric Oxide Synthase and Novel Phytochemicals.

Degree: PhD, 2006, Brigham Young University

 Cyclooxygenases (COXs) are of important therapeutic value as they are the target site of aspirin-like drugs. Here I report nine new COX-1 splice variants in… (more)

Subjects/Keywords: cyclooxygenase-1; cyclooxygenase-2; Chemistry

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APA (6th Edition):

Xu, Y. (2006). Studies on Cyclooxygenase-1, its Structure and Splice Variants, and Modulation of Cyclooxygenase-2 by Inducible Nitric Oxide Synthase and Novel Phytochemicals. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7208&context=etd

Chicago Manual of Style (16th Edition):

Xu, Yibing. “Studies on Cyclooxygenase-1, its Structure and Splice Variants, and Modulation of Cyclooxygenase-2 by Inducible Nitric Oxide Synthase and Novel Phytochemicals.” 2006. Doctoral Dissertation, Brigham Young University. Accessed April 18, 2021. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7208&context=etd.

MLA Handbook (7th Edition):

Xu, Yibing. “Studies on Cyclooxygenase-1, its Structure and Splice Variants, and Modulation of Cyclooxygenase-2 by Inducible Nitric Oxide Synthase and Novel Phytochemicals.” 2006. Web. 18 Apr 2021.

Vancouver:

Xu Y. Studies on Cyclooxygenase-1, its Structure and Splice Variants, and Modulation of Cyclooxygenase-2 by Inducible Nitric Oxide Synthase and Novel Phytochemicals. [Internet] [Doctoral dissertation]. Brigham Young University; 2006. [cited 2021 Apr 18]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7208&context=etd.

Council of Science Editors:

Xu Y. Studies on Cyclooxygenase-1, its Structure and Splice Variants, and Modulation of Cyclooxygenase-2 by Inducible Nitric Oxide Synthase and Novel Phytochemicals. [Doctoral Dissertation]. Brigham Young University; 2006. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=7208&context=etd


Vanderbilt University

6. Hermanson, Daniel John. Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects.

Degree: PhD, Chemistry, 2014, Vanderbilt University

 Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. Daniel John Hermanson Dissertation under the direction of Professor Lawrence J. Marnett Cyclooxygenase-2… (more)

Subjects/Keywords: pain; anxiety; cyclooxygenase-2; endocannabinoids; inflammation; NSAIDs

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APA (6th Edition):

Hermanson, D. J. (2014). Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11000

Chicago Manual of Style (16th Edition):

Hermanson, Daniel John. “Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed April 18, 2021. http://hdl.handle.net/1803/11000.

MLA Handbook (7th Edition):

Hermanson, Daniel John. “Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects.” 2014. Web. 18 Apr 2021.

Vancouver:

Hermanson DJ. Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1803/11000.

Council of Science Editors:

Hermanson DJ. Substrate-selective Inhibition of Cyclooxygenase-2: Molecular Determinants, Probe Development, and In Vivo Effects. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/11000


Nelson Mandela Metropolitan University

7. Fredericks, Ernst. Molecular signaling in colorectal carcinogenesis : the roles and relationships of beta-catenin, PPARgamma and COX-2.

Degree: PhD, Faculty of Science, 2013, Nelson Mandela Metropolitan University

 Colorectal cancer (CRC) is a common disease with significant morbidity and mortality. In spite of significant advances in understanding the molecular signaling in this disorder,… (more)

Subjects/Keywords: Colon (Anatomy)  – Cancer; Cyclooxygenase 2; Peroxisomes

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APA (6th Edition):

Fredericks, E. (2013). Molecular signaling in colorectal carcinogenesis : the roles and relationships of beta-catenin, PPARgamma and COX-2. (Doctoral Dissertation). Nelson Mandela Metropolitan University. Retrieved from http://hdl.handle.net/10948/d1021014

Chicago Manual of Style (16th Edition):

Fredericks, Ernst. “Molecular signaling in colorectal carcinogenesis : the roles and relationships of beta-catenin, PPARgamma and COX-2.” 2013. Doctoral Dissertation, Nelson Mandela Metropolitan University. Accessed April 18, 2021. http://hdl.handle.net/10948/d1021014.

MLA Handbook (7th Edition):

Fredericks, Ernst. “Molecular signaling in colorectal carcinogenesis : the roles and relationships of beta-catenin, PPARgamma and COX-2.” 2013. Web. 18 Apr 2021.

Vancouver:

Fredericks E. Molecular signaling in colorectal carcinogenesis : the roles and relationships of beta-catenin, PPARgamma and COX-2. [Internet] [Doctoral dissertation]. Nelson Mandela Metropolitan University; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10948/d1021014.

Council of Science Editors:

Fredericks E. Molecular signaling in colorectal carcinogenesis : the roles and relationships of beta-catenin, PPARgamma and COX-2. [Doctoral Dissertation]. Nelson Mandela Metropolitan University; 2013. Available from: http://hdl.handle.net/10948/d1021014


University of Guelph

8. Sim, Zhi Hui. Cyclooxygenase-2 expression in feline eyes with and without uveitis.

Degree: MS, Department of Clinical Studies, 2016, University of Guelph

 Uveitis is one of the leading causes of blindness in cats, and an important potential therapeutic target is cyclooxygenase-2 (COX-2). This case-control study aimed to… (more)

Subjects/Keywords: Cyclooxygenase-2; Feline eyes; Uveitis; Immunohistochemistry

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APA (6th Edition):

Sim, Z. H. (2016). Cyclooxygenase-2 expression in feline eyes with and without uveitis. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9718

Chicago Manual of Style (16th Edition):

Sim, Zhi Hui. “Cyclooxygenase-2 expression in feline eyes with and without uveitis.” 2016. Masters Thesis, University of Guelph. Accessed April 18, 2021. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9718.

MLA Handbook (7th Edition):

Sim, Zhi Hui. “Cyclooxygenase-2 expression in feline eyes with and without uveitis.” 2016. Web. 18 Apr 2021.

Vancouver:

Sim ZH. Cyclooxygenase-2 expression in feline eyes with and without uveitis. [Internet] [Masters thesis]. University of Guelph; 2016. [cited 2021 Apr 18]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9718.

Council of Science Editors:

Sim ZH. Cyclooxygenase-2 expression in feline eyes with and without uveitis. [Masters Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/9718


University of Ottawa

9. Thibodeau, Jean-François. Prostaglandin E2 Signaling Through Kidney EP1 and EP4 Receptors; Implications in Diabetes and Hypertension .

Degree: 2015, University of Ottawa

 Chronic kidney disease is defined as the appearance of kidney functional or structural injury. Cyclooxygenase and prostaglandin E2 have been implicated in the pathogenesis of… (more)

Subjects/Keywords: prostaglandin receptors; diabetic nephropathy; hypertension; cyclooxygenase

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APA (6th Edition):

Thibodeau, J. (2015). Prostaglandin E2 Signaling Through Kidney EP1 and EP4 Receptors; Implications in Diabetes and Hypertension . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32749

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):

Thibodeau, Jean-François. “Prostaglandin E2 Signaling Through Kidney EP1 and EP4 Receptors; Implications in Diabetes and Hypertension .” 2015. Thesis, University of Ottawa. Accessed April 18, 2021. http://hdl.handle.net/10393/32749.

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

MLA Handbook (7th Edition):

Thibodeau, Jean-François. “Prostaglandin E2 Signaling Through Kidney EP1 and EP4 Receptors; Implications in Diabetes and Hypertension .” 2015. Web. 18 Apr 2021.

Vancouver:

Thibodeau J. Prostaglandin E2 Signaling Through Kidney EP1 and EP4 Receptors; Implications in Diabetes and Hypertension . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10393/32749.

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

Council of Science Editors:

Thibodeau J. Prostaglandin E2 Signaling Through Kidney EP1 and EP4 Receptors; Implications in Diabetes and Hypertension . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32749

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


University of Arizona

10. Basudhar, Debashree. NITROGEN OXIDE RELEASING PRODRUGS AS ANTIINFLAMMATORY, ANTICANCER AND CARDIOPROTECTIVE AGENTS .

Degree: 2011, University of Arizona

 This dissertation focuses on chemical and biological evaluation of diazeniumdiolate based nitrogen oxide releasing prodrugs. Three projects are described. i. Synthesis and biological evaluation of… (more)

Subjects/Keywords: aspirin; cancer; Cyclooxygenase; Nitric oxide; Nitroxyl; NSAID

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APA (6th Edition):

Basudhar, D. (2011). NITROGEN OXIDE RELEASING PRODRUGS AS ANTIINFLAMMATORY, ANTICANCER AND CARDIOPROTECTIVE AGENTS . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/145745

Chicago Manual of Style (16th Edition):

Basudhar, Debashree. “NITROGEN OXIDE RELEASING PRODRUGS AS ANTIINFLAMMATORY, ANTICANCER AND CARDIOPROTECTIVE AGENTS .” 2011. Doctoral Dissertation, University of Arizona. Accessed April 18, 2021. http://hdl.handle.net/10150/145745.

MLA Handbook (7th Edition):

Basudhar, Debashree. “NITROGEN OXIDE RELEASING PRODRUGS AS ANTIINFLAMMATORY, ANTICANCER AND CARDIOPROTECTIVE AGENTS .” 2011. Web. 18 Apr 2021.

Vancouver:

Basudhar D. NITROGEN OXIDE RELEASING PRODRUGS AS ANTIINFLAMMATORY, ANTICANCER AND CARDIOPROTECTIVE AGENTS . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10150/145745.

Council of Science Editors:

Basudhar D. NITROGEN OXIDE RELEASING PRODRUGS AS ANTIINFLAMMATORY, ANTICANCER AND CARDIOPROTECTIVE AGENTS . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/145745


University of Cambridge

11. Arthur, Sabastine. Identification of host cellular factors that regulate human norovirus replication.

Degree: PhD, 2020, University of Cambridge

 The human norovirus (HuNoV) is one of the most predominant causes of gastroenteritis, yet no suitable therapeutics are available for its control. Currently, our knowledge… (more)

Subjects/Keywords: Interferon Lamda; Hsp90; Human norovirus; Cyclooxygenase; Replicons

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APA (6th Edition):

Arthur, S. (2020). Identification of host cellular factors that regulate human norovirus replication. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/315713

Chicago Manual of Style (16th Edition):

Arthur, Sabastine. “Identification of host cellular factors that regulate human norovirus replication.” 2020. Doctoral Dissertation, University of Cambridge. Accessed April 18, 2021. https://www.repository.cam.ac.uk/handle/1810/315713.

MLA Handbook (7th Edition):

Arthur, Sabastine. “Identification of host cellular factors that regulate human norovirus replication.” 2020. Web. 18 Apr 2021.

Vancouver:

Arthur S. Identification of host cellular factors that regulate human norovirus replication. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 Apr 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/315713.

Council of Science Editors:

Arthur S. Identification of host cellular factors that regulate human norovirus replication. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/315713


Johannes Gutenberg Universität Mainz

12. Gellner, Katrin. Das Phosphoproteom von Plattenepithelkarzinomen des Kopf-Hals-Bereichs nach Bestrahlung und Applikation des Cyclooxygenase-Inhibitors Flurbiprofen.

Degree: 2012, Johannes Gutenberg Universität Mainz

Ziel: Die Radiotherapie hat in der Behandlung von Plattenepithelkarzinomen des Kopf- und Halsbereichs nach wie vor einen hohen Stellenwert. Der Erfolg eines Therapieregimes, das die… (more)

Subjects/Keywords: Phosphoproteom, HNSCC, Bestrahlung, Cyclooxygenase-Inhibitor; phosphoproteome, HNSCC, irradiation, cyclooxygenase-inhibitor; Medical sciences Medicine

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APA (6th Edition):

Gellner, K. (2012). Das Phosphoproteom von Plattenepithelkarzinomen des Kopf-Hals-Bereichs nach Bestrahlung und Applikation des Cyclooxygenase-Inhibitors Flurbiprofen. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3336/

Chicago Manual of Style (16th Edition):

Gellner, Katrin. “Das Phosphoproteom von Plattenepithelkarzinomen des Kopf-Hals-Bereichs nach Bestrahlung und Applikation des Cyclooxygenase-Inhibitors Flurbiprofen.” 2012. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed April 18, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2013/3336/.

MLA Handbook (7th Edition):

Gellner, Katrin. “Das Phosphoproteom von Plattenepithelkarzinomen des Kopf-Hals-Bereichs nach Bestrahlung und Applikation des Cyclooxygenase-Inhibitors Flurbiprofen.” 2012. Web. 18 Apr 2021.

Vancouver:

Gellner K. Das Phosphoproteom von Plattenepithelkarzinomen des Kopf-Hals-Bereichs nach Bestrahlung und Applikation des Cyclooxygenase-Inhibitors Flurbiprofen. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2012. [cited 2021 Apr 18]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3336/.

Council of Science Editors:

Gellner K. Das Phosphoproteom von Plattenepithelkarzinomen des Kopf-Hals-Bereichs nach Bestrahlung und Applikation des Cyclooxygenase-Inhibitors Flurbiprofen. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2012. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3336/

13. Ghewa, El Achkar. Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2 : Anti-inflammatory properties of statins, triterpenoids and thiazole derivatives : role of heme oxygenase-1 (HO-1) and cyclooxygenase-2 (COX-2).

Degree: Docteur es, Biologie cellulaire et moléculaire, 2015, Université Paris-Est

 Les statines sont des inhibiteurs sélectifs de la 3-hydroxy-3-méthylglutaryl-coenzyme A réductase, utilisées pour diminuer la biosynthèse du cholestérol. Ces molécules possèdent en plus de leur… (more)

Subjects/Keywords: Inflammation; Statines; Heme oxygenase; Cucurbitacine; Cyclooxygenase; Thiazole; Inflammation; Statins; Heme oxygenase; Cucurbitacin; Cyclooxygenase; Thiazol; 615

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APA (6th Edition):

Ghewa, E. A. (2015). Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2 : Anti-inflammatory properties of statins, triterpenoids and thiazole derivatives : role of heme oxygenase-1 (HO-1) and cyclooxygenase-2 (COX-2). (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2015PESC0033

Chicago Manual of Style (16th Edition):

Ghewa, El Achkar. “Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2 : Anti-inflammatory properties of statins, triterpenoids and thiazole derivatives : role of heme oxygenase-1 (HO-1) and cyclooxygenase-2 (COX-2).” 2015. Doctoral Dissertation, Université Paris-Est. Accessed April 18, 2021. http://www.theses.fr/2015PESC0033.

MLA Handbook (7th Edition):

Ghewa, El Achkar. “Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2 : Anti-inflammatory properties of statins, triterpenoids and thiazole derivatives : role of heme oxygenase-1 (HO-1) and cyclooxygenase-2 (COX-2).” 2015. Web. 18 Apr 2021.

Vancouver:

Ghewa EA. Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2 : Anti-inflammatory properties of statins, triterpenoids and thiazole derivatives : role of heme oxygenase-1 (HO-1) and cyclooxygenase-2 (COX-2). [Internet] [Doctoral dissertation]. Université Paris-Est; 2015. [cited 2021 Apr 18]. Available from: http://www.theses.fr/2015PESC0033.

Council of Science Editors:

Ghewa EA. Propriétés anti-inflammatoires des statines, des triterpénoïdes et des dérivés de thiazole : rôle de la hème-oxygénase-1 et de la cyclooxygénase-2 : Anti-inflammatory properties of statins, triterpenoids and thiazole derivatives : role of heme oxygenase-1 (HO-1) and cyclooxygenase-2 (COX-2). [Doctoral Dissertation]. Université Paris-Est; 2015. Available from: http://www.theses.fr/2015PESC0033

14. Gagnaire, Aurelie. Rôle de la voie COX-2 au cours de l'infection par Brucella : Investigating the involvement of the COX-2 pathway during Brucella infection.

Degree: Docteur es, Biologie, 2016, Aix Marseille Université

Brucella est une bactérie intracellulaire facultative à Gram négatif responsable d’une zoonose, la brucellose. Pour persister dans l’organisme, Brucella agit comme un pathogène furtif en… (more)

Subjects/Keywords: Brucella; Cyclooxygenase-2; Ptgs2; Cellules dendritiques; Infection intradermale; Maladies infectieuses; Brucella; Cyclooxygenase-2; Ptgs2; Dendritic cells; Intradermal infection; Infectious diseases; 570

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APA (6th Edition):

Gagnaire, A. (2016). Rôle de la voie COX-2 au cours de l'infection par Brucella : Investigating the involvement of the COX-2 pathway during Brucella infection. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2016AIXM4054

Chicago Manual of Style (16th Edition):

Gagnaire, Aurelie. “Rôle de la voie COX-2 au cours de l'infection par Brucella : Investigating the involvement of the COX-2 pathway during Brucella infection.” 2016. Doctoral Dissertation, Aix Marseille Université. Accessed April 18, 2021. http://www.theses.fr/2016AIXM4054.

MLA Handbook (7th Edition):

Gagnaire, Aurelie. “Rôle de la voie COX-2 au cours de l'infection par Brucella : Investigating the involvement of the COX-2 pathway during Brucella infection.” 2016. Web. 18 Apr 2021.

Vancouver:

Gagnaire A. Rôle de la voie COX-2 au cours de l'infection par Brucella : Investigating the involvement of the COX-2 pathway during Brucella infection. [Internet] [Doctoral dissertation]. Aix Marseille Université 2016. [cited 2021 Apr 18]. Available from: http://www.theses.fr/2016AIXM4054.

Council of Science Editors:

Gagnaire A. Rôle de la voie COX-2 au cours de l'infection par Brucella : Investigating the involvement of the COX-2 pathway during Brucella infection. [Doctoral Dissertation]. Aix Marseille Université 2016. Available from: http://www.theses.fr/2016AIXM4054

15. Paulo Roberto Gabbai Armelin. Modelagem molecular de derivados pirimidínicos e estudos de docking nas enzimas ciclooxigenase 1 e ciclooxigenase 2.

Degree: 2010, Universidade Federal de São Carlos

Neste trabalho, o docking molecular foi utilizado para o estudo da formação de complexos alvoligante das enzimas Ciclooxigenase 1 (COX-1) e Ciclooxigenase 2 (COX-2) com… (more)

Subjects/Keywords: Biotecnologia; Ciclooxigenase 1; Ciclooxigenase 2; Pirimidinas; Docking; Docking; OUTROS; Modelagem molecular; Cyclooxygenase 1; Cyclooxygenase 2; Pyrimidines; Molecular modeling

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APA (6th Edition):

Armelin, P. R. G. (2010). Modelagem molecular de derivados pirimidínicos e estudos de docking nas enzimas ciclooxigenase 1 e ciclooxigenase 2. (Thesis). Universidade Federal de São Carlos. Retrieved from http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=4191

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):

Armelin, Paulo Roberto Gabbai. “Modelagem molecular de derivados pirimidínicos e estudos de docking nas enzimas ciclooxigenase 1 e ciclooxigenase 2.” 2010. Thesis, Universidade Federal de São Carlos. Accessed April 18, 2021. http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=4191.

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

MLA Handbook (7th Edition):

Armelin, Paulo Roberto Gabbai. “Modelagem molecular de derivados pirimidínicos e estudos de docking nas enzimas ciclooxigenase 1 e ciclooxigenase 2.” 2010. Web. 18 Apr 2021.

Vancouver:

Armelin PRG. Modelagem molecular de derivados pirimidínicos e estudos de docking nas enzimas ciclooxigenase 1 e ciclooxigenase 2. [Internet] [Thesis]. Universidade Federal de São Carlos; 2010. [cited 2021 Apr 18]. Available from: http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=4191.

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

Council of Science Editors:

Armelin PRG. Modelagem molecular de derivados pirimidínicos e estudos de docking nas enzimas ciclooxigenase 1 e ciclooxigenase 2. [Thesis]. Universidade Federal de São Carlos; 2010. Available from: http://www.bdtd.ufscar.br/htdocs/tedeSimplificado//tde_busca/arquivo.php?codArquivo=4191

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


University of Toronto

16. Winnett, Brenton Paul Lauder Coverdale. The Role of NSAIDs in Impaired Osseointegration in Dental Implant Prosthodontics.

Degree: 2013, University of Toronto

Objective: To appraise whether adverse events following oral implant placement may be associated with peri-operative use of non-steroidal anti-inflammatory drugs (NSAIDs). Methods: All patients with… (more)

Subjects/Keywords: Dental Implants; Anti-Inflammatory Agents, Non-Steroidal; Dental Restoration Failure; Cyclooxygenase 1; Cyclooxygenase 2; Osseointegration; 0567; 0564; 0766

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APA (6th Edition):

Winnett, B. P. L. C. (2013). The Role of NSAIDs in Impaired Osseointegration in Dental Implant Prosthodontics. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43335

Chicago Manual of Style (16th Edition):

Winnett, Brenton Paul Lauder Coverdale. “The Role of NSAIDs in Impaired Osseointegration in Dental Implant Prosthodontics.” 2013. Masters Thesis, University of Toronto. Accessed April 18, 2021. http://hdl.handle.net/1807/43335.

MLA Handbook (7th Edition):

Winnett, Brenton Paul Lauder Coverdale. “The Role of NSAIDs in Impaired Osseointegration in Dental Implant Prosthodontics.” 2013. Web. 18 Apr 2021.

Vancouver:

Winnett BPLC. The Role of NSAIDs in Impaired Osseointegration in Dental Implant Prosthodontics. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1807/43335.

Council of Science Editors:

Winnett BPLC. The Role of NSAIDs in Impaired Osseointegration in Dental Implant Prosthodontics. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43335


Technical University of Lisbon

17. Marques, Daniela Cristina Sobreiro. Avaliação da expressão da Cox-2 em tumores mamários de cadela.

Degree: 2013, Technical University of Lisbon

Dissertação de Mestrado Integrado em Medicina Veterinária

A ciclooxigenase-2 (COX-2) é uma proteína que se encontra envolvida na oncogénese e na inflamação, tendo sido demonstrada… (more)

Subjects/Keywords: Ciclooxigenase-2; tumor mamário; cadela; cyclooxygenase-2; mammary tumour; bitch

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APA (6th Edition):

Marques, D. C. S. (2013). Avaliação da expressão da Cox-2 em tumores mamários de cadela. (Thesis). Technical University of Lisbon. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/6222

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):

Marques, Daniela Cristina Sobreiro. “Avaliação da expressão da Cox-2 em tumores mamários de cadela.” 2013. Thesis, Technical University of Lisbon. Accessed April 18, 2021. http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/6222.

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

MLA Handbook (7th Edition):

Marques, Daniela Cristina Sobreiro. “Avaliação da expressão da Cox-2 em tumores mamários de cadela.” 2013. Web. 18 Apr 2021.

Vancouver:

Marques DCS. Avaliação da expressão da Cox-2 em tumores mamários de cadela. [Internet] [Thesis]. Technical University of Lisbon; 2013. [cited 2021 Apr 18]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/6222.

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

Council of Science Editors:

Marques DCS. Avaliação da expressão da Cox-2 em tumores mamários de cadela. [Thesis]. Technical University of Lisbon; 2013. Available from: http://www.rcaap.pt/detail.jsp?id=oai:www.repository.utl.pt:10400.5/6222

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


NSYSU

18. Chu, Tian-huei. Therapeutic Efficacy and Mechanism of Celecoxib for Hepatocellular Carcinoma.

Degree: PhD, Institute of Biomedical Sciences, 2014, NSYSU

 Hepatocellular carcinoma (HCC) is the one of most common malignancies in Taiwan. Current HCC therapies include surgery, chemotherapy, radiofrequency ablation and target therapy. However, the… (more)

Subjects/Keywords: cyclooxygenase 2; sorafenib; cancer stem cells; celecoxib; hepatocellular carcinoma

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APA (6th Edition):

Chu, T. (2014). Therapeutic Efficacy and Mechanism of Celecoxib for Hepatocellular Carcinoma. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809114-182128

Chicago Manual of Style (16th Edition):

Chu, Tian-huei. “Therapeutic Efficacy and Mechanism of Celecoxib for Hepatocellular Carcinoma.” 2014. Doctoral Dissertation, NSYSU. Accessed April 18, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809114-182128.

MLA Handbook (7th Edition):

Chu, Tian-huei. “Therapeutic Efficacy and Mechanism of Celecoxib for Hepatocellular Carcinoma.” 2014. Web. 18 Apr 2021.

Vancouver:

Chu T. Therapeutic Efficacy and Mechanism of Celecoxib for Hepatocellular Carcinoma. [Internet] [Doctoral dissertation]. NSYSU; 2014. [cited 2021 Apr 18]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809114-182128.

Council of Science Editors:

Chu T. Therapeutic Efficacy and Mechanism of Celecoxib for Hepatocellular Carcinoma. [Doctoral Dissertation]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0809114-182128


NSYSU

19. Ho, Ying-Hao. Peripheral inflammation increases seizure susceptibility via the induction of neuroinflammation and oxidative stress in the hippocampus.

Degree: PhD, Biological Sciences, 2015, NSYSU

 Epilepsy is a common neurological disorder. Neuroinflammation is involved in the pathophysiology of epilepsy. Tissue oxidative stress is another confounding factor in epilepsy. While both… (more)

Subjects/Keywords: Neuroinflammation; Proinflammatory cytokines; Cyclooxygenase-2; Oxidative stress; Seizure; Hippocampus; Peripheral inflammation

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APA (6th Edition):

Ho, Y. (2015). Peripheral inflammation increases seizure susceptibility via the induction of neuroinflammation and oxidative stress in the hippocampus. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720115-114205

Chicago Manual of Style (16th Edition):

Ho, Ying-Hao. “Peripheral inflammation increases seizure susceptibility via the induction of neuroinflammation and oxidative stress in the hippocampus.” 2015. Doctoral Dissertation, NSYSU. Accessed April 18, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720115-114205.

MLA Handbook (7th Edition):

Ho, Ying-Hao. “Peripheral inflammation increases seizure susceptibility via the induction of neuroinflammation and oxidative stress in the hippocampus.” 2015. Web. 18 Apr 2021.

Vancouver:

Ho Y. Peripheral inflammation increases seizure susceptibility via the induction of neuroinflammation and oxidative stress in the hippocampus. [Internet] [Doctoral dissertation]. NSYSU; 2015. [cited 2021 Apr 18]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720115-114205.

Council of Science Editors:

Ho Y. Peripheral inflammation increases seizure susceptibility via the induction of neuroinflammation and oxidative stress in the hippocampus. [Doctoral Dissertation]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0720115-114205


Universiteit Utrecht

20. Schenning, M. Phosphatidylinositol transfer proteins in cell survival and apoptosis.

Degree: 2007, Universiteit Utrecht

 Mouse fibroblast cells overexpressing phosphatidylinositol transfer protein alpha [PI-TPalpha; sense PI-TPalpha (SPIalpha) cells] show a significantly increased rate of proliferation and an extreme resistance toward… (more)

Subjects/Keywords: Scheikunde; phosphatidylinositol transfer protein; cyclooxygenase 2; proliferation; eicosanoids; endocannabinoid; apoptosis; prostaglandins

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APA (6th Edition):

Schenning, M. (2007). Phosphatidylinositol transfer proteins in cell survival and apoptosis. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/21526

Chicago Manual of Style (16th Edition):

Schenning, M. “Phosphatidylinositol transfer proteins in cell survival and apoptosis.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed April 18, 2021. http://dspace.library.uu.nl:8080/handle/1874/21526.

MLA Handbook (7th Edition):

Schenning, M. “Phosphatidylinositol transfer proteins in cell survival and apoptosis.” 2007. Web. 18 Apr 2021.

Vancouver:

Schenning M. Phosphatidylinositol transfer proteins in cell survival and apoptosis. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2021 Apr 18]. Available from: http://dspace.library.uu.nl:8080/handle/1874/21526.

Council of Science Editors:

Schenning M. Phosphatidylinositol transfer proteins in cell survival and apoptosis. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/21526


University of Utah

21. Doyle, Kelly. Oxidation of peroxiredoxins and carbonylation of class I histone deacetylases by arachidonic acid metabolites.

Degree: PhD, Medicinal Chemistry;, 2010, University of Utah

 Redox signaling is a mechanism that facilitates homeostasis during redox insult resulting from cellular respiration, defense, and inflammation. Cellular perception of, and adaptation to redox… (more)

Subjects/Keywords: Cyclooxygenase; Cyclopentenone; Histone deacetylase; Lipoxygenase; Peroxiredoxin; Redox Biochemistry

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APA (6th Edition):

Doyle, K. (2010). Oxidation of peroxiredoxins and carbonylation of class I histone deacetylases by arachidonic acid metabolites. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/930/rec/853

Chicago Manual of Style (16th Edition):

Doyle, Kelly. “Oxidation of peroxiredoxins and carbonylation of class I histone deacetylases by arachidonic acid metabolites.” 2010. Doctoral Dissertation, University of Utah. Accessed April 18, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/930/rec/853.

MLA Handbook (7th Edition):

Doyle, Kelly. “Oxidation of peroxiredoxins and carbonylation of class I histone deacetylases by arachidonic acid metabolites.” 2010. Web. 18 Apr 2021.

Vancouver:

Doyle K. Oxidation of peroxiredoxins and carbonylation of class I histone deacetylases by arachidonic acid metabolites. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2021 Apr 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/930/rec/853.

Council of Science Editors:

Doyle K. Oxidation of peroxiredoxins and carbonylation of class I histone deacetylases by arachidonic acid metabolites. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/930/rec/853

22. Kawakita, Fumihiro. Effects of Toll-Like Receptor 4 Antagonists Against Cerebral Vasospasm After Experimental Subarachnoid Hemorrhage in Mice.

Degree: 博士(医学), 2017, Mie University / 三重大学

Toll-like receptor 4 (TLR4) signaling may play a crucial role in the occurrence of cerebral vasospasm after subarachnoid hemorrhage (SAH). The main purpose of this… (more)

Subjects/Keywords: Cerebral vasospasm; Cyclooxygenase-1; Subarachnoid hemorrhage; Toll-like receptor 4

Page 1 Page 2 Page 3

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APA (6th Edition):

Kawakita, F. (2017). Effects of Toll-Like Receptor 4 Antagonists Against Cerebral Vasospasm After Experimental Subarachnoid Hemorrhage in Mice. (Thesis). Mie University / 三重大学. Retrieved from http://hdl.handle.net/10076/00017131

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):

Kawakita, Fumihiro. “Effects of Toll-Like Receptor 4 Antagonists Against Cerebral Vasospasm After Experimental Subarachnoid Hemorrhage in Mice.” 2017. Thesis, Mie University / 三重大学. Accessed April 18, 2021. http://hdl.handle.net/10076/00017131.

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

MLA Handbook (7th Edition):

Kawakita, Fumihiro. “Effects of Toll-Like Receptor 4 Antagonists Against Cerebral Vasospasm After Experimental Subarachnoid Hemorrhage in Mice.” 2017. Web. 18 Apr 2021.

Vancouver:

Kawakita F. Effects of Toll-Like Receptor 4 Antagonists Against Cerebral Vasospasm After Experimental Subarachnoid Hemorrhage in Mice. [Internet] [Thesis]. Mie University / 三重大学; 2017. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10076/00017131.

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

Council of Science Editors:

Kawakita F. Effects of Toll-Like Receptor 4 Antagonists Against Cerebral Vasospasm After Experimental Subarachnoid Hemorrhage in Mice. [Thesis]. Mie University / 三重大学; 2017. Available from: http://hdl.handle.net/10076/00017131

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


University of Rochester

23. Ghosh, Simantini; O'Banion, M. Kerry. The Effect of Sustained Overexpression of Interleukin-1β on Pathology in Murine Models of Alzheimer’s disease and Tauopathy.

Degree: PhD, 2014, University of Rochester

 Alzheimer’s disease (AD) is the most common form of dementia in the elderly and is marked by extraneuronal beta Amyloid (Aβ) plaques and intraneuronal tangles… (more)

Subjects/Keywords: 3xTgAD; IL-1β; Interleukin; Microglia; Tau; JNPL3; COX-1; SC560; Cyclooxygenase

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APA (6th Edition):

Ghosh, Simantini; O'Banion, M. K. (2014). The Effect of Sustained Overexpression of Interleukin-1β on Pathology in Murine Models of Alzheimer’s disease and Tauopathy. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/28434

Chicago Manual of Style (16th Edition):

Ghosh, Simantini; O'Banion, M Kerry. “The Effect of Sustained Overexpression of Interleukin-1β on Pathology in Murine Models of Alzheimer’s disease and Tauopathy.” 2014. Doctoral Dissertation, University of Rochester. Accessed April 18, 2021. http://hdl.handle.net/1802/28434.

MLA Handbook (7th Edition):

Ghosh, Simantini; O'Banion, M Kerry. “The Effect of Sustained Overexpression of Interleukin-1β on Pathology in Murine Models of Alzheimer’s disease and Tauopathy.” 2014. Web. 18 Apr 2021.

Vancouver:

Ghosh, Simantini; O'Banion MK. The Effect of Sustained Overexpression of Interleukin-1β on Pathology in Murine Models of Alzheimer’s disease and Tauopathy. [Internet] [Doctoral dissertation]. University of Rochester; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1802/28434.

Council of Science Editors:

Ghosh, Simantini; O'Banion MK. The Effect of Sustained Overexpression of Interleukin-1β on Pathology in Murine Models of Alzheimer’s disease and Tauopathy. [Doctoral Dissertation]. University of Rochester; 2014. Available from: http://hdl.handle.net/1802/28434


University of Alberta

24. Tietz, Ole. Novel radiotracers for the molecular imaging of cyclooxygenase-2 (COX-2) using positron emission tomography (PET).

Degree: PhD, Department of Oncology, 2015, University of Alberta

 Cancer remains one of the most prevalent causes of death in the western world. Effective treatment of this disease relies on the ability to diagnose… (more)

Subjects/Keywords: cyclooxygenase-2 (COX-2); positron emission tomography (PET)

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APA (6th Edition):

Tietz, O. (2015). Novel radiotracers for the molecular imaging of cyclooxygenase-2 (COX-2) using positron emission tomography (PET). (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/ccv43nx04g

Chicago Manual of Style (16th Edition):

Tietz, Ole. “Novel radiotracers for the molecular imaging of cyclooxygenase-2 (COX-2) using positron emission tomography (PET).” 2015. Doctoral Dissertation, University of Alberta. Accessed April 18, 2021. https://era.library.ualberta.ca/files/ccv43nx04g.

MLA Handbook (7th Edition):

Tietz, Ole. “Novel radiotracers for the molecular imaging of cyclooxygenase-2 (COX-2) using positron emission tomography (PET).” 2015. Web. 18 Apr 2021.

Vancouver:

Tietz O. Novel radiotracers for the molecular imaging of cyclooxygenase-2 (COX-2) using positron emission tomography (PET). [Internet] [Doctoral dissertation]. University of Alberta; 2015. [cited 2021 Apr 18]. Available from: https://era.library.ualberta.ca/files/ccv43nx04g.

Council of Science Editors:

Tietz O. Novel radiotracers for the molecular imaging of cyclooxygenase-2 (COX-2) using positron emission tomography (PET). [Doctoral Dissertation]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/ccv43nx04g


Vanderbilt University

25. Duggan, Kelsey Constance. Structural and Functional Analysis of Cyclooxygenase-2 Inhibition by Non-Steroidal Anti-Inflammatory Drugs.

Degree: PhD, Biochemistry, 2011, Vanderbilt University

 The cyclooxygenase enzymes (COX-1 and COX-2) catalyze the conversion arachidonic acid (AA) to prostaglandin H2 (PGH2), which is the precursor to biologically active prostanoids. The… (more)

Subjects/Keywords: naproxen; prostaglandins; cyclooxygenase; non-steroidal anti-inflammatory drugs

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APA (6th Edition):

Duggan, K. C. (2011). Structural and Functional Analysis of Cyclooxygenase-2 Inhibition by Non-Steroidal Anti-Inflammatory Drugs. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10425

Chicago Manual of Style (16th Edition):

Duggan, Kelsey Constance. “Structural and Functional Analysis of Cyclooxygenase-2 Inhibition by Non-Steroidal Anti-Inflammatory Drugs.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed April 18, 2021. http://hdl.handle.net/1803/10425.

MLA Handbook (7th Edition):

Duggan, Kelsey Constance. “Structural and Functional Analysis of Cyclooxygenase-2 Inhibition by Non-Steroidal Anti-Inflammatory Drugs.” 2011. Web. 18 Apr 2021.

Vancouver:

Duggan KC. Structural and Functional Analysis of Cyclooxygenase-2 Inhibition by Non-Steroidal Anti-Inflammatory Drugs. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1803/10425.

Council of Science Editors:

Duggan KC. Structural and Functional Analysis of Cyclooxygenase-2 Inhibition by Non-Steroidal Anti-Inflammatory Drugs. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/10425


Vanderbilt University

26. Mitchener, Michelle Marie. A. Competition and allostery govern substrate selectivity of cyclooxygenase-2 B. Enzymatic oxidation of M1dG in the genome.

Degree: PhD, Chemistry, 2017, Vanderbilt University

 Part A: Cyclooxygenase-2 (COX-2) oxygenates arachidonic acid (AA) and its ester analog, 2-arachidonoylglycerol (2-AG), to prostaglandins (PGs) and prostaglandin glyceryl esters (PG-Gs), respectively. Although the… (more)

Subjects/Keywords: M1dG; chemical kinetics; endocannabinoids; cyclooxygenase-2; DNA adducts

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APA (6th Edition):

Mitchener, M. M. (2017). A. Competition and allostery govern substrate selectivity of cyclooxygenase-2 B. Enzymatic oxidation of M1dG in the genome. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15119

Chicago Manual of Style (16th Edition):

Mitchener, Michelle Marie. “A. Competition and allostery govern substrate selectivity of cyclooxygenase-2 B. Enzymatic oxidation of M1dG in the genome.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed April 18, 2021. http://hdl.handle.net/1803/15119.

MLA Handbook (7th Edition):

Mitchener, Michelle Marie. “A. Competition and allostery govern substrate selectivity of cyclooxygenase-2 B. Enzymatic oxidation of M1dG in the genome.” 2017. Web. 18 Apr 2021.

Vancouver:

Mitchener MM. A. Competition and allostery govern substrate selectivity of cyclooxygenase-2 B. Enzymatic oxidation of M1dG in the genome. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1803/15119.

Council of Science Editors:

Mitchener MM. A. Competition and allostery govern substrate selectivity of cyclooxygenase-2 B. Enzymatic oxidation of M1dG in the genome. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/15119


Vanderbilt University

27. Shockley, Erin Michelle. Biochemical Reaction Networks from a Systems Biology Perspective.

Degree: PhD, Chemical and Physical Biology, 2019, Vanderbilt University

 Cells constantly sense and respond to cues via signaling networks. These networks operate in dynamic systems and often serve multiple purposes, translating multiple inputs into… (more)

Subjects/Keywords: systems biology; cyclooxygenase-2; biological modeling; bayesian analysis; network analysis

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APA (6th Edition):

Shockley, E. M. (2019). Biochemical Reaction Networks from a Systems Biology Perspective. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10918

Chicago Manual of Style (16th Edition):

Shockley, Erin Michelle. “Biochemical Reaction Networks from a Systems Biology Perspective.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed April 18, 2021. http://hdl.handle.net/1803/10918.

MLA Handbook (7th Edition):

Shockley, Erin Michelle. “Biochemical Reaction Networks from a Systems Biology Perspective.” 2019. Web. 18 Apr 2021.

Vancouver:

Shockley EM. Biochemical Reaction Networks from a Systems Biology Perspective. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1803/10918.

Council of Science Editors:

Shockley EM. Biochemical Reaction Networks from a Systems Biology Perspective. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/10918

28. REILA TAINÁ MENDES. EFEITOS CARDIOVASCULARES DA INIBIÇÃO DA CICLOOXIGENASE-2 EM UM MODELO EXPERIMENTAL DE PERIODONTITE INDUZIDA POR LIGADURA.

Degree: 2012, UNIVERSIDADE ESTADUAL DE PONTA GROSSA

A periodontite é uma doença inflamatória crônica iniciada e perpetuada por bactérias anaeróbicas gram-negativas que colonizam a área subgengival. Esta doença é caracterizada pela destruição… (more)

Subjects/Keywords: Periodontite; Ciclooxigenase-2; Endotélio Vascular; Periodontitis; Cyclooxygenase-2; Vascular Endothelium; ODONTOLOGIA

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APA (6th Edition):

MENDES, R. T. (2012). EFEITOS CARDIOVASCULARES DA INIBIÇÃO DA CICLOOXIGENASE-2 EM UM MODELO EXPERIMENTAL DE PERIODONTITE INDUZIDA POR LIGADURA. (Thesis). UNIVERSIDADE ESTADUAL DE PONTA GROSSA. Retrieved from http://www.bicen-tede.uepg.br/tde_busca/arquivo.php?codArquivo=736

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):

MENDES, REILA TAINÁ. “EFEITOS CARDIOVASCULARES DA INIBIÇÃO DA CICLOOXIGENASE-2 EM UM MODELO EXPERIMENTAL DE PERIODONTITE INDUZIDA POR LIGADURA.” 2012. Thesis, UNIVERSIDADE ESTADUAL DE PONTA GROSSA. Accessed April 18, 2021. http://www.bicen-tede.uepg.br/tde_busca/arquivo.php?codArquivo=736.

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

MLA Handbook (7th Edition):

MENDES, REILA TAINÁ. “EFEITOS CARDIOVASCULARES DA INIBIÇÃO DA CICLOOXIGENASE-2 EM UM MODELO EXPERIMENTAL DE PERIODONTITE INDUZIDA POR LIGADURA.” 2012. Web. 18 Apr 2021.

Vancouver:

MENDES RT. EFEITOS CARDIOVASCULARES DA INIBIÇÃO DA CICLOOXIGENASE-2 EM UM MODELO EXPERIMENTAL DE PERIODONTITE INDUZIDA POR LIGADURA. [Internet] [Thesis]. UNIVERSIDADE ESTADUAL DE PONTA GROSSA; 2012. [cited 2021 Apr 18]. Available from: http://www.bicen-tede.uepg.br/tde_busca/arquivo.php?codArquivo=736.

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

Council of Science Editors:

MENDES RT. EFEITOS CARDIOVASCULARES DA INIBIÇÃO DA CICLOOXIGENASE-2 EM UM MODELO EXPERIMENTAL DE PERIODONTITE INDUZIDA POR LIGADURA. [Thesis]. UNIVERSIDADE ESTADUAL DE PONTA GROSSA; 2012. Available from: http://www.bicen-tede.uepg.br/tde_busca/arquivo.php?codArquivo=736

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


Texas A&M University

29. Li, Min. Constrictor prostanoid-potentiated vascular contraction: regulation of endothelial and vascular smooth muscle mechanism by estrogen.

Degree: PhD, Veterinary Physiology, 2004, Texas A&M University

 The objectives of this research were to elucidate the involvement of constrictor prostanoids in the vascular reactivity to vasopressin (VP) and the role of estrogen… (more)

Subjects/Keywords: estrogen; thromboxane; aorta; rat; cyclooxygenase

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

APA (6th Edition):

Li, M. (2004). Constrictor prostanoid-potentiated vascular contraction: regulation of endothelial and vascular smooth muscle mechanism by estrogen. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/549

Chicago Manual of Style (16th Edition):

Li, Min. “Constrictor prostanoid-potentiated vascular contraction: regulation of endothelial and vascular smooth muscle mechanism by estrogen.” 2004. Doctoral Dissertation, Texas A&M University. Accessed April 18, 2021. http://hdl.handle.net/1969.1/549.

MLA Handbook (7th Edition):

Li, Min. “Constrictor prostanoid-potentiated vascular contraction: regulation of endothelial and vascular smooth muscle mechanism by estrogen.” 2004. Web. 18 Apr 2021.

Vancouver:

Li M. Constrictor prostanoid-potentiated vascular contraction: regulation of endothelial and vascular smooth muscle mechanism by estrogen. [Internet] [Doctoral dissertation]. Texas A&M University; 2004. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1969.1/549.

Council of Science Editors:

Li M. Constrictor prostanoid-potentiated vascular contraction: regulation of endothelial and vascular smooth muscle mechanism by estrogen. [Doctoral Dissertation]. Texas A&M University; 2004. Available from: http://hdl.handle.net/1969.1/549


North Carolina State University

30. Tomlinson, Julia Elizabeth. Cyclooxygenase Inhibitors Affect Recovery of Ischemic-injured Jejunum.

Degree: PhD, Physiology, 2005, North Carolina State University

 he cyclooxygenase (COX) enzyme produces prostaglandins. There are 3 isoforms of COX (including COX-1 and COX-2). As prostaglandins are involved in intestinal repair, the objective… (more)

Subjects/Keywords: cyclooxygenase; NSAID; intestine; equine; ischemia

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APA (6th Edition):

Tomlinson, J. E. (2005). Cyclooxygenase Inhibitors Affect Recovery of Ischemic-injured Jejunum. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/4741

Chicago Manual of Style (16th Edition):

Tomlinson, Julia Elizabeth. “Cyclooxygenase Inhibitors Affect Recovery of Ischemic-injured Jejunum.” 2005. Doctoral Dissertation, North Carolina State University. Accessed April 18, 2021. http://www.lib.ncsu.edu/resolver/1840.16/4741.

MLA Handbook (7th Edition):

Tomlinson, Julia Elizabeth. “Cyclooxygenase Inhibitors Affect Recovery of Ischemic-injured Jejunum.” 2005. Web. 18 Apr 2021.

Vancouver:

Tomlinson JE. Cyclooxygenase Inhibitors Affect Recovery of Ischemic-injured Jejunum. [Internet] [Doctoral dissertation]. North Carolina State University; 2005. [cited 2021 Apr 18]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4741.

Council of Science Editors:

Tomlinson JE. Cyclooxygenase Inhibitors Affect Recovery of Ischemic-injured Jejunum. [Doctoral Dissertation]. North Carolina State University; 2005. Available from: http://www.lib.ncsu.edu/resolver/1840.16/4741

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