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You searched for subject:(Eicosanoids). Showing records 1 – 30 of 54 total matches.

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University of Illinois – Urbana-Champaign

1. Meling, Daryl Duane. Protein-protein interactions and mechanistic insights for CYP2J2 and CYP5A1.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

Eicosanoids are signaling molecules formed from the oxidation of -3 and -6 fatty acids. CYP2J2 and CYP5A1 are two key enzymes involved in the formation… (more)

Subjects/Keywords: eicosanoids; cytochrome P450s

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APA (6th Edition):

Meling, D. D. (2016). Protein-protein interactions and mechanistic insights for CYP2J2 and CYP5A1. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90774

Chicago Manual of Style (16th Edition):

Meling, Daryl Duane. “Protein-protein interactions and mechanistic insights for CYP2J2 and CYP5A1.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed August 09, 2020. http://hdl.handle.net/2142/90774.

MLA Handbook (7th Edition):

Meling, Daryl Duane. “Protein-protein interactions and mechanistic insights for CYP2J2 and CYP5A1.” 2016. Web. 09 Aug 2020.

Vancouver:

Meling DD. Protein-protein interactions and mechanistic insights for CYP2J2 and CYP5A1. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/2142/90774.

Council of Science Editors:

Meling DD. Protein-protein interactions and mechanistic insights for CYP2J2 and CYP5A1. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90774


University of Manitoba

2. Shi, Hong. Effects of conjugated linoleic acid isomers on eicosanoid metabolism in kidney and liver tissues of obese zucker rats.

Degree: Human Nutritional Sciences, 2011, University of Manitoba

 Seventeen wk old male obese Zucker rats were given 0.4% (w/w) conjugated linoleic acid (CLA) isomers for 8 wk to determine effects of specific isomers… (more)

Subjects/Keywords: CLA; Zucker rat; eicosanoids; tissues

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APA (6th Edition):

Shi, H. (2011). Effects of conjugated linoleic acid isomers on eicosanoid metabolism in kidney and liver tissues of obese zucker rats. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4971

Chicago Manual of Style (16th Edition):

Shi, Hong. “Effects of conjugated linoleic acid isomers on eicosanoid metabolism in kidney and liver tissues of obese zucker rats.” 2011. Masters Thesis, University of Manitoba. Accessed August 09, 2020. http://hdl.handle.net/1993/4971.

MLA Handbook (7th Edition):

Shi, Hong. “Effects of conjugated linoleic acid isomers on eicosanoid metabolism in kidney and liver tissues of obese zucker rats.” 2011. Web. 09 Aug 2020.

Vancouver:

Shi H. Effects of conjugated linoleic acid isomers on eicosanoid metabolism in kidney and liver tissues of obese zucker rats. [Internet] [Masters thesis]. University of Manitoba; 2011. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/1993/4971.

Council of Science Editors:

Shi H. Effects of conjugated linoleic acid isomers on eicosanoid metabolism in kidney and liver tissues of obese zucker rats. [Masters Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4971


University of Missouri – Columbia

3. Cunningham, Anna Maria. Immune Mediators of Murine Lyme Arthritis.

Degree: 2014, University of Missouri – Columbia

 Lyme disease is the most common vector-borne disease in both the United States and Europe; however, its pathogenesis is incompletely understood. The studies described in… (more)

Subjects/Keywords: Lyme disease; Eicosanoids  – Pathophysiology; Arthritis

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APA (6th Edition):

Cunningham, A. M. (2014). Immune Mediators of Murine Lyme Arthritis. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/45872

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):

Cunningham, Anna Maria. “Immune Mediators of Murine Lyme Arthritis.” 2014. Thesis, University of Missouri – Columbia. Accessed August 09, 2020. http://hdl.handle.net/10355/45872.

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

MLA Handbook (7th Edition):

Cunningham, Anna Maria. “Immune Mediators of Murine Lyme Arthritis.” 2014. Web. 09 Aug 2020.

Vancouver:

Cunningham AM. Immune Mediators of Murine Lyme Arthritis. [Internet] [Thesis]. University of Missouri – Columbia; 2014. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/10355/45872.

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

Council of Science Editors:

Cunningham AM. Immune Mediators of Murine Lyme Arthritis. [Thesis]. University of Missouri – Columbia; 2014. Available from: http://hdl.handle.net/10355/45872

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


University of Kansas

4. Johnson, Ryan Tyler. Advances and Applications of Capillary Electrophoresis-Mass Spectrometry.

Degree: PhD, Chemistry, 2016, University of Kansas

 Capillary electrophoresis-mass spectrometry (CE-MS) is a useful analytical technique capable of high efficiency separations from complex and low volume samples. However, the interface between CE… (more)

Subjects/Keywords: Analytical chemistry; Biochemistry; Capillary Electrophoresis; Eicosanoids; Flavonoids; Interface; Mass Spectrometry; Sheathless

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APA (6th Edition):

Johnson, R. T. (2016). Advances and Applications of Capillary Electrophoresis-Mass Spectrometry. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/24202

Chicago Manual of Style (16th Edition):

Johnson, Ryan Tyler. “Advances and Applications of Capillary Electrophoresis-Mass Spectrometry.” 2016. Doctoral Dissertation, University of Kansas. Accessed August 09, 2020. http://hdl.handle.net/1808/24202.

MLA Handbook (7th Edition):

Johnson, Ryan Tyler. “Advances and Applications of Capillary Electrophoresis-Mass Spectrometry.” 2016. Web. 09 Aug 2020.

Vancouver:

Johnson RT. Advances and Applications of Capillary Electrophoresis-Mass Spectrometry. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/1808/24202.

Council of Science Editors:

Johnson RT. Advances and Applications of Capillary Electrophoresis-Mass Spectrometry. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/24202


Universiteit Utrecht

5. 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 August 09, 2020. 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. 09 Aug 2020.

Vancouver:

Schenning M. Phosphatidylinositol transfer proteins in cell survival and apoptosis. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2020 Aug 09]. 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


Montana Tech

6. Wang, Rong. Analysis of eicosanoids released from activated macrophages.

Degree: MS, 1998, Montana Tech

Subjects/Keywords: Eicosanoids.; Arachidonic acid.; Macrophages.

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APA (6th Edition):

Wang, R. (1998). Analysis of eicosanoids released from activated macrophages. (Masters Thesis). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/6653

Chicago Manual of Style (16th Edition):

Wang, Rong. “Analysis of eicosanoids released from activated macrophages.” 1998. Masters Thesis, Montana Tech. Accessed August 09, 2020. https://scholarworks.umt.edu/etd/6653.

MLA Handbook (7th Edition):

Wang, Rong. “Analysis of eicosanoids released from activated macrophages.” 1998. Web. 09 Aug 2020.

Vancouver:

Wang R. Analysis of eicosanoids released from activated macrophages. [Internet] [Masters thesis]. Montana Tech; 1998. [cited 2020 Aug 09]. Available from: https://scholarworks.umt.edu/etd/6653.

Council of Science Editors:

Wang R. Analysis of eicosanoids released from activated macrophages. [Masters Thesis]. Montana Tech; 1998. Available from: https://scholarworks.umt.edu/etd/6653


University of Stirling

7. Collier, Ian D. Towards the synthesis of fluoro-thromboxane A₂ analogues.

Degree: PhD, 1988, University of Stirling

 Firstly, the biosynthesis and physiological role of thromboxanes and the potential for a thromboxane A₂ antagonist in cardiovascular therapy are discussed. Secondly, the importance of… (more)

Subjects/Keywords: Thromboxanes Analysis; Eicosanoids; Prostanoids

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APA (6th Edition):

Collier, I. D. (1988). Towards the synthesis of fluoro-thromboxane A₂ analogues. (Doctoral Dissertation). University of Stirling. Retrieved from http://hdl.handle.net/1893/31181

Chicago Manual of Style (16th Edition):

Collier, Ian D. “Towards the synthesis of fluoro-thromboxane A₂ analogues.” 1988. Doctoral Dissertation, University of Stirling. Accessed August 09, 2020. http://hdl.handle.net/1893/31181.

MLA Handbook (7th Edition):

Collier, Ian D. “Towards the synthesis of fluoro-thromboxane A₂ analogues.” 1988. Web. 09 Aug 2020.

Vancouver:

Collier ID. Towards the synthesis of fluoro-thromboxane A₂ analogues. [Internet] [Doctoral dissertation]. University of Stirling; 1988. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/1893/31181.

Council of Science Editors:

Collier ID. Towards the synthesis of fluoro-thromboxane A₂ analogues. [Doctoral Dissertation]. University of Stirling; 1988. Available from: http://hdl.handle.net/1893/31181


UCLA

8. Solaimani, Parrisa Sherry. RNAi High Throughput Screenings Facilitate the Identification of Proteins Necessary for TCDD-induced CYP1A1 Enzymatic Activity and Aid in the Discovery of a Novel Role for Sin3A in AHR-Mediated Gene Expression.

Degree: Molecular Toxicology, 2012, UCLA

 The aryl hydrocarbon receptor (AHR) pathway is activated upon exposure to environmental pollutants 2,3,7,8-tetrachlorodibenzo-�-dioxin (TCDD) and benzo[a]pyrene (B[a]P), which leads to the induced expression of… (more)

Subjects/Keywords: Toxicology; Genetics; Molecular biology; AHR; CYP1A1; CYP2S1; Eicosanoids; High Throughput Screening; TCDD

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APA (6th Edition):

Solaimani, P. S. (2012). RNAi High Throughput Screenings Facilitate the Identification of Proteins Necessary for TCDD-induced CYP1A1 Enzymatic Activity and Aid in the Discovery of a Novel Role for Sin3A in AHR-Mediated Gene Expression. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/39p7h68f

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):

Solaimani, Parrisa Sherry. “RNAi High Throughput Screenings Facilitate the Identification of Proteins Necessary for TCDD-induced CYP1A1 Enzymatic Activity and Aid in the Discovery of a Novel Role for Sin3A in AHR-Mediated Gene Expression.” 2012. Thesis, UCLA. Accessed August 09, 2020. http://www.escholarship.org/uc/item/39p7h68f.

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

MLA Handbook (7th Edition):

Solaimani, Parrisa Sherry. “RNAi High Throughput Screenings Facilitate the Identification of Proteins Necessary for TCDD-induced CYP1A1 Enzymatic Activity and Aid in the Discovery of a Novel Role for Sin3A in AHR-Mediated Gene Expression.” 2012. Web. 09 Aug 2020.

Vancouver:

Solaimani PS. RNAi High Throughput Screenings Facilitate the Identification of Proteins Necessary for TCDD-induced CYP1A1 Enzymatic Activity and Aid in the Discovery of a Novel Role for Sin3A in AHR-Mediated Gene Expression. [Internet] [Thesis]. UCLA; 2012. [cited 2020 Aug 09]. Available from: http://www.escholarship.org/uc/item/39p7h68f.

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

Council of Science Editors:

Solaimani PS. RNAi High Throughput Screenings Facilitate the Identification of Proteins Necessary for TCDD-induced CYP1A1 Enzymatic Activity and Aid in the Discovery of a Novel Role for Sin3A in AHR-Mediated Gene Expression. [Thesis]. UCLA; 2012. Available from: http://www.escholarship.org/uc/item/39p7h68f

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

9. Stevanatto, Pollyana Bulgarelli. Análise do papel das ciclooxigenases 1 e 2 na migração da linhagem celular de glioma humano U251-MG.

Degree: Mestrado, Biologia Celular e Tecidual, 2013, University of São Paulo

O glioblastoma multiforme (GBM) é um dos gliomas mais comuns, classificado como um glioma de grau IV (Organização Mundial da Saúde - OMS) e notoriamente… (more)

Subjects/Keywords: Antiinflamatórios não-esteróides; Eicosanóides; Eicosanoids; Glioblastoma multiforme; Glioblastoma multiforme; Neoplasias; Neoplasms; NSAIDs; Prostaglandinas; Prostaglandins

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APA (6th Edition):

Stevanatto, P. B. (2013). Análise do papel das ciclooxigenases 1 e 2 na migração da linhagem celular de glioma humano U251-MG. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-17062013-085430/ ;

Chicago Manual of Style (16th Edition):

Stevanatto, Pollyana Bulgarelli. “Análise do papel das ciclooxigenases 1 e 2 na migração da linhagem celular de glioma humano U251-MG.” 2013. Masters Thesis, University of São Paulo. Accessed August 09, 2020. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-17062013-085430/ ;.

MLA Handbook (7th Edition):

Stevanatto, Pollyana Bulgarelli. “Análise do papel das ciclooxigenases 1 e 2 na migração da linhagem celular de glioma humano U251-MG.” 2013. Web. 09 Aug 2020.

Vancouver:

Stevanatto PB. Análise do papel das ciclooxigenases 1 e 2 na migração da linhagem celular de glioma humano U251-MG. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2020 Aug 09]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-17062013-085430/ ;.

Council of Science Editors:

Stevanatto PB. Análise do papel das ciclooxigenases 1 e 2 na migração da linhagem celular de glioma humano U251-MG. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-17062013-085430/ ;

10. Souto, Pollyana Cristina Maggio de Castro. Caracterização da reação inflamatória induzida pelo veneno da serpente Bothrops insularis: Influxo leucocitário, liberação de mediadores inflamatórios e mecanismos envolvidos nesses efeitos.

Degree: Mestrado, Farmacologia, 2010, University of São Paulo

Este estudo teve por objetivos: i) caracterizar o influxo leucocitário induzido pelo veneno de Bothrops insularis (VBi); ii) avaliar a liberação de PGD2 e PGE2,… (more)

Subjects/Keywords: Bothrops insularis; Bothrops insularis; Ciclooxigenases; Ciclooxygenases; Eicosanóides; Eicosanoids; Leucócitos; Leukocytes; Lipooxigenases; Lipooxygenases

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APA (6th Edition):

Souto, P. C. M. d. C. (2010). Caracterização da reação inflamatória induzida pelo veneno da serpente Bothrops insularis: Influxo leucocitário, liberação de mediadores inflamatórios e mecanismos envolvidos nesses efeitos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42136/tde-25032010-151949/ ;

Chicago Manual of Style (16th Edition):

Souto, Pollyana Cristina Maggio de Castro. “Caracterização da reação inflamatória induzida pelo veneno da serpente Bothrops insularis: Influxo leucocitário, liberação de mediadores inflamatórios e mecanismos envolvidos nesses efeitos.” 2010. Masters Thesis, University of São Paulo. Accessed August 09, 2020. http://www.teses.usp.br/teses/disponiveis/42/42136/tde-25032010-151949/ ;.

MLA Handbook (7th Edition):

Souto, Pollyana Cristina Maggio de Castro. “Caracterização da reação inflamatória induzida pelo veneno da serpente Bothrops insularis: Influxo leucocitário, liberação de mediadores inflamatórios e mecanismos envolvidos nesses efeitos.” 2010. Web. 09 Aug 2020.

Vancouver:

Souto PCMdC. Caracterização da reação inflamatória induzida pelo veneno da serpente Bothrops insularis: Influxo leucocitário, liberação de mediadores inflamatórios e mecanismos envolvidos nesses efeitos. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Aug 09]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42136/tde-25032010-151949/ ;.

Council of Science Editors:

Souto PCMdC. Caracterização da reação inflamatória induzida pelo veneno da serpente Bothrops insularis: Influxo leucocitário, liberação de mediadores inflamatórios e mecanismos envolvidos nesses efeitos. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/42/42136/tde-25032010-151949/ ;


University of Pennsylvania

11. Snyder, Nathaniel W. Investigations of Bioactivity, Disposition, and Metabolism of Lipids Through Liquid Chromatography-Mass Spectrometry.

Degree: 2013, University of Pennsylvania

 Inflammatory diseases and multiple human cancers are associated with increased cyclooxygenase-2 (COX-2) expression together with decreased expression of 15-hydroxyprostaglandin dehydrogenase (15-PGDH). This has been hypothesized… (more)

Subjects/Keywords: eicosanoids; lipidomics; liquid chromatography; mass spectrometry; Analytical Chemistry; Biochemistry; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Snyder, N. W. (2013). Investigations of Bioactivity, Disposition, and Metabolism of Lipids Through Liquid Chromatography-Mass Spectrometry. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/929

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):

Snyder, Nathaniel W. “Investigations of Bioactivity, Disposition, and Metabolism of Lipids Through Liquid Chromatography-Mass Spectrometry.” 2013. Thesis, University of Pennsylvania. Accessed August 09, 2020. https://repository.upenn.edu/edissertations/929.

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

MLA Handbook (7th Edition):

Snyder, Nathaniel W. “Investigations of Bioactivity, Disposition, and Metabolism of Lipids Through Liquid Chromatography-Mass Spectrometry.” 2013. Web. 09 Aug 2020.

Vancouver:

Snyder NW. Investigations of Bioactivity, Disposition, and Metabolism of Lipids Through Liquid Chromatography-Mass Spectrometry. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2020 Aug 09]. Available from: https://repository.upenn.edu/edissertations/929.

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

Council of Science Editors:

Snyder NW. Investigations of Bioactivity, Disposition, and Metabolism of Lipids Through Liquid Chromatography-Mass Spectrometry. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/929

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


University of Toronto

12. Lin, Lauren. The Effect of a Low n-6 Polyunsaturated Fatty Acid Diet on the Rate of Loss of Arachidonic Acid and Docosahexaenoic Acid from Rat Brain Phospholipids.

Degree: 2014, University of Toronto

Arachidonic acid (ARA) and docosahexaenoic acid (DHA) are the predominant n-6 and n-3 polyunsaturated fatty acids (PUFA) in the brain, and alterations in their metabolism… (more)

Subjects/Keywords: brain; eicosanoids; intracerebroventricular infusion; n-6 polyunsaturated fatty acid; phospholipids; rate of loss; 0570

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APA (6th Edition):

Lin, L. (2014). The Effect of a Low n-6 Polyunsaturated Fatty Acid Diet on the Rate of Loss of Arachidonic Acid and Docosahexaenoic Acid from Rat Brain Phospholipids. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67937

Chicago Manual of Style (16th Edition):

Lin, Lauren. “The Effect of a Low n-6 Polyunsaturated Fatty Acid Diet on the Rate of Loss of Arachidonic Acid and Docosahexaenoic Acid from Rat Brain Phospholipids.” 2014. Masters Thesis, University of Toronto. Accessed August 09, 2020. http://hdl.handle.net/1807/67937.

MLA Handbook (7th Edition):

Lin, Lauren. “The Effect of a Low n-6 Polyunsaturated Fatty Acid Diet on the Rate of Loss of Arachidonic Acid and Docosahexaenoic Acid from Rat Brain Phospholipids.” 2014. Web. 09 Aug 2020.

Vancouver:

Lin L. The Effect of a Low n-6 Polyunsaturated Fatty Acid Diet on the Rate of Loss of Arachidonic Acid and Docosahexaenoic Acid from Rat Brain Phospholipids. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/1807/67937.

Council of Science Editors:

Lin L. The Effect of a Low n-6 Polyunsaturated Fatty Acid Diet on the Rate of Loss of Arachidonic Acid and Docosahexaenoic Acid from Rat Brain Phospholipids. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67937


University of Tennessee – Knoxville

13. Rett, Brian. Increasing Dietary Linoleic Acid Does Not Increase Tissue Arachidonic Acid Content in Adults Consuming Western- Type Diets.

Degree: MS, Nutrition, 2011, University of Tennessee – Knoxville

  Linoleic acid, with a DRI of 12-17g/d, is the most highly consumed polyunsaturated fatty acid in the Western diet and is found in virtually… (more)

Subjects/Keywords: linoleic acid; arachidonic acid; eicosanoids; n-6; omega-6; Medicine and Health Sciences

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APA (6th Edition):

Rett, B. (2011). Increasing Dietary Linoleic Acid Does Not Increase Tissue Arachidonic Acid Content in Adults Consuming Western- Type Diets. (Thesis). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_gradthes/908

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):

Rett, Brian. “Increasing Dietary Linoleic Acid Does Not Increase Tissue Arachidonic Acid Content in Adults Consuming Western- Type Diets.” 2011. Thesis, University of Tennessee – Knoxville. Accessed August 09, 2020. https://trace.tennessee.edu/utk_gradthes/908.

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

MLA Handbook (7th Edition):

Rett, Brian. “Increasing Dietary Linoleic Acid Does Not Increase Tissue Arachidonic Acid Content in Adults Consuming Western- Type Diets.” 2011. Web. 09 Aug 2020.

Vancouver:

Rett B. Increasing Dietary Linoleic Acid Does Not Increase Tissue Arachidonic Acid Content in Adults Consuming Western- Type Diets. [Internet] [Thesis]. University of Tennessee – Knoxville; 2011. [cited 2020 Aug 09]. Available from: https://trace.tennessee.edu/utk_gradthes/908.

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

Council of Science Editors:

Rett B. Increasing Dietary Linoleic Acid Does Not Increase Tissue Arachidonic Acid Content in Adults Consuming Western- Type Diets. [Thesis]. University of Tennessee – Knoxville; 2011. Available from: https://trace.tennessee.edu/utk_gradthes/908

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


Penn State University

14. Chiaro, Christopher Richard. Identification of Endogenous Modulators for the Aryl Hydrocarbon Receptor.

Degree: PhD, Genetics, 2007, Penn State University

 The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor capable of being regulated by a structurally diverse array of chemicals ranging from environmental carcinogens… (more)

Subjects/Keywords: leukotrienes; eicosanoids; dioxins; TCDD; AhR; DiHETEs; HETEs

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APA (6th Edition):

Chiaro, C. R. (2007). Identification of Endogenous Modulators for the Aryl Hydrocarbon Receptor. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8032

Chicago Manual of Style (16th Edition):

Chiaro, Christopher Richard. “Identification of Endogenous Modulators for the Aryl Hydrocarbon Receptor.” 2007. Doctoral Dissertation, Penn State University. Accessed August 09, 2020. https://etda.libraries.psu.edu/catalog/8032.

MLA Handbook (7th Edition):

Chiaro, Christopher Richard. “Identification of Endogenous Modulators for the Aryl Hydrocarbon Receptor.” 2007. Web. 09 Aug 2020.

Vancouver:

Chiaro CR. Identification of Endogenous Modulators for the Aryl Hydrocarbon Receptor. [Internet] [Doctoral dissertation]. Penn State University; 2007. [cited 2020 Aug 09]. Available from: https://etda.libraries.psu.edu/catalog/8032.

Council of Science Editors:

Chiaro CR. Identification of Endogenous Modulators for the Aryl Hydrocarbon Receptor. [Doctoral Dissertation]. Penn State University; 2007. Available from: https://etda.libraries.psu.edu/catalog/8032

15. Luciana de Souza Moreira. Estudo da modulação de corpúsculos lipídicos em células epiteliais.

Degree: 2007, Fundação Oswaldo Cruz

Corpúsculos lipídicos (CLs) são inclusões citoplasmáticas compostas principalmente por triglicerídeos e ésteres de colesterol, sendo também depósitos intracelulares de ácido araquidônico (AA) que pode ser… (more)

Subjects/Keywords: Ácido Araquidônico; Células Epiteliais; Eicosanóides; Dinoprostona; Células Sanguíneas; BIOLOGIA MOLECULAR; Bovino; Humano; Arachidonic Acid; Epithelial Cells; Eicosanoids; Dinoprostone; Blood Cells

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APA (6th Edition):

Moreira, L. d. S. (2007). Estudo da modulação de corpúsculos lipídicos em células epiteliais. (Thesis). Fundação Oswaldo Cruz. Retrieved from http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=110

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):

Moreira, Luciana de Souza. “Estudo da modulação de corpúsculos lipídicos em células epiteliais.” 2007. Thesis, Fundação Oswaldo Cruz. Accessed August 09, 2020. http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=110.

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

MLA Handbook (7th Edition):

Moreira, Luciana de Souza. “Estudo da modulação de corpúsculos lipídicos em células epiteliais.” 2007. Web. 09 Aug 2020.

Vancouver:

Moreira LdS. Estudo da modulação de corpúsculos lipídicos em células epiteliais. [Internet] [Thesis]. Fundação Oswaldo Cruz; 2007. [cited 2020 Aug 09]. Available from: http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=110.

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

Council of Science Editors:

Moreira LdS. Estudo da modulação de corpúsculos lipídicos em células epiteliais. [Thesis]. Fundação Oswaldo Cruz; 2007. Available from: http://www.bdtd.cict.fiocruz.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=110

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

16. Feitoza, Fábio. Estudo in vitro do efeito da prostaglandina E2 na migração das células U87MG e U251MG, evidenciando a matriz extracelular e as moléculas de adesão.

Degree: Mestrado, Biologia Celular e Tecidual, 2014, University of São Paulo

O glioblastoma multiforme (GBM) é uma neoplasia do sistema nervoso central (SNC), caracterizada por uma elevada capacidade proliferativa e migratória. O desenvolvimento do tumor provoca… (more)

Subjects/Keywords: Adhesion molecules; Cell migration; Eicosanoides; Eicosanoids; Extracellular matrix; Glioblastoma multiforme; Glioma; Matriz extracelular; Migração; Moléculas de adesão

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APA (6th Edition):

Feitoza, F. (2014). Estudo in vitro do efeito da prostaglandina E2 na migração das células U87MG e U251MG, evidenciando a matriz extracelular e as moléculas de adesão. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-26062014-194701/ ;

Chicago Manual of Style (16th Edition):

Feitoza, Fábio. “Estudo in vitro do efeito da prostaglandina E2 na migração das células U87MG e U251MG, evidenciando a matriz extracelular e as moléculas de adesão.” 2014. Masters Thesis, University of São Paulo. Accessed August 09, 2020. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-26062014-194701/ ;.

MLA Handbook (7th Edition):

Feitoza, Fábio. “Estudo in vitro do efeito da prostaglandina E2 na migração das células U87MG e U251MG, evidenciando a matriz extracelular e as moléculas de adesão.” 2014. Web. 09 Aug 2020.

Vancouver:

Feitoza F. Estudo in vitro do efeito da prostaglandina E2 na migração das células U87MG e U251MG, evidenciando a matriz extracelular e as moléculas de adesão. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2020 Aug 09]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-26062014-194701/ ;.

Council of Science Editors:

Feitoza F. Estudo in vitro do efeito da prostaglandina E2 na migração das células U87MG e U251MG, evidenciando a matriz extracelular e as moléculas de adesão. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-26062014-194701/ ;

17. Rodrigues, Lilian Cataldi. Participação da galectina-1 na evolução da histoplasmose experimental.

Degree: Mestrado, Biociências Aplicadas à Farmácia, 2007, University of São Paulo

 A galectina-1 (Gal-1) pertence a uma família de lectinas endógenas que reconhecem ß-galactosídeos e atuam em vários processos biológicos. A Gal-1 pode modular a resposta… (more)

Subjects/Keywords: citocinas; cytokines; eicosanóides; eicosanoids; galectin-1; galectina-1; Histoplasma capsulatum; Histoplasma capsulatum; immunological response; inflamação; inflammation; modulação da resposta imunológica

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APA (6th Edition):

Rodrigues, L. C. (2007). Participação da galectina-1 na evolução da histoplasmose experimental. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60135/tde-01042009-133835/ ;

Chicago Manual of Style (16th Edition):

Rodrigues, Lilian Cataldi. “Participação da galectina-1 na evolução da histoplasmose experimental.” 2007. Masters Thesis, University of São Paulo. Accessed August 09, 2020. http://www.teses.usp.br/teses/disponiveis/60/60135/tde-01042009-133835/ ;.

MLA Handbook (7th Edition):

Rodrigues, Lilian Cataldi. “Participação da galectina-1 na evolução da histoplasmose experimental.” 2007. Web. 09 Aug 2020.

Vancouver:

Rodrigues LC. Participação da galectina-1 na evolução da histoplasmose experimental. [Internet] [Masters thesis]. University of São Paulo; 2007. [cited 2020 Aug 09]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-01042009-133835/ ;.

Council of Science Editors:

Rodrigues LC. Participação da galectina-1 na evolução da histoplasmose experimental. [Masters Thesis]. University of São Paulo; 2007. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-01042009-133835/ ;

18. Ferreira, Matthew Thomas. Analysis of how the production and activity of PGD2 affects glioma cell lines.

Degree: Mestrado, Biologia Celular e Tecidual, 2015, University of São Paulo

The World Health Organization classifies glioblastoma (GBM) as a type IV astrocytoma, making it one of the most fatal tumors that exists. Despite the advances… (more)

Subjects/Keywords: Cancer; Câncer; Eicosanoides; Eicosanoids; Glioblastoma; Glioblastoma; Opposing roles; Papeis opostos; PGD2; PGD2; PGE2; PGE2; Prostaglandin; Prostaglandina

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APA (6th Edition):

Ferreira, M. T. (2015). Analysis of how the production and activity of PGD2 affects glioma cell lines. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42134/tde-10042015-120110/ ;

Chicago Manual of Style (16th Edition):

Ferreira, Matthew Thomas. “Analysis of how the production and activity of PGD2 affects glioma cell lines.” 2015. Masters Thesis, University of São Paulo. Accessed August 09, 2020. http://www.teses.usp.br/teses/disponiveis/42/42134/tde-10042015-120110/ ;.

MLA Handbook (7th Edition):

Ferreira, Matthew Thomas. “Analysis of how the production and activity of PGD2 affects glioma cell lines.” 2015. Web. 09 Aug 2020.

Vancouver:

Ferreira MT. Analysis of how the production and activity of PGD2 affects glioma cell lines. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2020 Aug 09]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-10042015-120110/ ;.

Council of Science Editors:

Ferreira MT. Analysis of how the production and activity of PGD2 affects glioma cell lines. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/42/42134/tde-10042015-120110/ ;

19. Prage, Edward B. Structural Studies of Inhibition of the Human Inducible Prostaglandin E Synthase MPGES1.

Degree: PhD, Chemistry, 2012, Vanderbilt University

 The inducible enzyme microsomal prostaglandin E synthase 1 (MPGES1) is a glutathione-dependent prostaglandin H2 isomerase that has been implicated in a variety of inflammatory diseases… (more)

Subjects/Keywords: MAPEG; Eicosanoids; Inflammation; MPGES1; H/D Exchange

…23 11. Cytochrome P450-derived Eicosanoids… …the benefit of those who suffer from inflammatory diseases. Eicosanoids Metabolites of… …is eikosi, arachidonic acid-derived mediators are referred to as eicosanoids. Eicosanoids… …Signaling molecules that are derived from arachidonic acid are known as eicosanoids. 6… …classes of eicosanoids. Cytochrome P450 (CYP) enzymes utilize arachidonic acid as a… 

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APA (6th Edition):

Prage, E. B. (2012). Structural Studies of Inhibition of the Human Inducible Prostaglandin E Synthase MPGES1. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-02202012-105424/ ;

Chicago Manual of Style (16th Edition):

Prage, Edward B. “Structural Studies of Inhibition of the Human Inducible Prostaglandin E Synthase MPGES1.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed August 09, 2020. http://etd.library.vanderbilt.edu/available/etd-02202012-105424/ ;.

MLA Handbook (7th Edition):

Prage, Edward B. “Structural Studies of Inhibition of the Human Inducible Prostaglandin E Synthase MPGES1.” 2012. Web. 09 Aug 2020.

Vancouver:

Prage EB. Structural Studies of Inhibition of the Human Inducible Prostaglandin E Synthase MPGES1. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Aug 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-02202012-105424/ ;.

Council of Science Editors:

Prage EB. Structural Studies of Inhibition of the Human Inducible Prostaglandin E Synthase MPGES1. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu/available/etd-02202012-105424/ ;

20. MAINAK MAL. Metabolic profiling of colorectal cancer.

Degree: 2011, National University of Singapore

Subjects/Keywords: colorectal cancer; metabolic profiling; metabolites; eicosanoids; mass spectrometry; biomarkers

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APA (6th Edition):

MAL, M. (2011). Metabolic profiling of colorectal cancer. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/29946

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):

MAL, MAINAK. “Metabolic profiling of colorectal cancer.” 2011. Thesis, National University of Singapore. Accessed August 09, 2020. http://scholarbank.nus.edu.sg/handle/10635/29946.

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

MLA Handbook (7th Edition):

MAL, MAINAK. “Metabolic profiling of colorectal cancer.” 2011. Web. 09 Aug 2020.

Vancouver:

MAL M. Metabolic profiling of colorectal cancer. [Internet] [Thesis]. National University of Singapore; 2011. [cited 2020 Aug 09]. Available from: http://scholarbank.nus.edu.sg/handle/10635/29946.

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

Council of Science Editors:

MAL M. Metabolic profiling of colorectal cancer. [Thesis]. National University of Singapore; 2011. Available from: http://scholarbank.nus.edu.sg/handle/10635/29946

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


Freie Universität Berlin

21. Adel, Susan. Mechanistic aspects of lipoxygenase evolution.

Degree: 2016, Freie Universität Berlin

 Introduction: Lipoxygenases (LOXn) form a family of lipid peroxidizing enzymes, which are widely distributed in plants and animals. Unfortunately, there is no unifying concept for… (more)

Subjects/Keywords: 5-lipoxygenase; 15-lipoxygenase; reaction specificity; eicosanoids; evolution; inflammation; antiinflammatory agents; cancer; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Adel, S. (2016). Mechanistic aspects of lipoxygenase evolution. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-10527

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):

Adel, Susan. “Mechanistic aspects of lipoxygenase evolution.” 2016. Thesis, Freie Universität Berlin. Accessed August 09, 2020. http://dx.doi.org/10.17169/refubium-10527.

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

MLA Handbook (7th Edition):

Adel, Susan. “Mechanistic aspects of lipoxygenase evolution.” 2016. Web. 09 Aug 2020.

Vancouver:

Adel S. Mechanistic aspects of lipoxygenase evolution. [Internet] [Thesis]. Freie Universität Berlin; 2016. [cited 2020 Aug 09]. Available from: http://dx.doi.org/10.17169/refubium-10527.

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

Council of Science Editors:

Adel S. Mechanistic aspects of lipoxygenase evolution. [Thesis]. Freie Universität Berlin; 2016. Available from: http://dx.doi.org/10.17169/refubium-10527

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


Freie Universität Berlin

22. Zhu, Ye. Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI).

Degree: 2015, Freie Universität Berlin

 Hintergrund und Hypothese: Ischämie-bedingtes akutes Nierenversagen (ANV) kann als schwerwiegende Komplikation in verschiedenen klinischen Situationen auftreten und führt zu erhöhter Morbidität und Mortalität der Patienten.… (more)

Subjects/Keywords: cytochrome P450 (CYP); dependent eicosanoids; acute kidney injury (AKI); 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Zhu, Y. (2015). Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI). (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-6041

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):

Zhu, Ye. “Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI).” 2015. Thesis, Freie Universität Berlin. Accessed August 09, 2020. http://dx.doi.org/10.17169/refubium-6041.

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

MLA Handbook (7th Edition):

Zhu, Ye. “Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI).” 2015. Web. 09 Aug 2020.

Vancouver:

Zhu Y. Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI). [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2020 Aug 09]. Available from: http://dx.doi.org/10.17169/refubium-6041.

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

Council of Science Editors:

Zhu Y. Rolle von Cytochrom P450 (CYP) -abhängigen Eicosanoide bei der experimentellen akuten Nierenschädigung (AKI). [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-6041

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

23. Duflot, Thomas. Rôle de l'époxyde hydrolase soluble dans les maladies cardiovasculaires. : Role of soluble epoxide hydrolase in cardiovascular diseases.

Degree: Docteur es, Aspects moleculaires et cellulaires de la biologie, 2018, Normandie

L’époxyde hydrolase soluble (sEH) est une enzyme ubiquitaire, bifonctionnelle, codée par le gène EPHX2. La partie hydrolase (sEH-H) est responsable de la dégradation de facteurs… (more)

Subjects/Keywords: Epoxyde hydrolase soluble; Maladies cardiovasculaires; Endothélium; Eicosanoïdes; Phospholipides; Soluble epoxide hydrolase; Cardiovascular diseases; Endothelium; Eicosanoids; Phospholipids; 610; 570

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APA (6th Edition):

Duflot, T. (2018). Rôle de l'époxyde hydrolase soluble dans les maladies cardiovasculaires. : Role of soluble epoxide hydrolase in cardiovascular diseases. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2018NORMR037

Chicago Manual of Style (16th Edition):

Duflot, Thomas. “Rôle de l'époxyde hydrolase soluble dans les maladies cardiovasculaires. : Role of soluble epoxide hydrolase in cardiovascular diseases.” 2018. Doctoral Dissertation, Normandie. Accessed August 09, 2020. http://www.theses.fr/2018NORMR037.

MLA Handbook (7th Edition):

Duflot, Thomas. “Rôle de l'époxyde hydrolase soluble dans les maladies cardiovasculaires. : Role of soluble epoxide hydrolase in cardiovascular diseases.” 2018. Web. 09 Aug 2020.

Vancouver:

Duflot T. Rôle de l'époxyde hydrolase soluble dans les maladies cardiovasculaires. : Role of soluble epoxide hydrolase in cardiovascular diseases. [Internet] [Doctoral dissertation]. Normandie; 2018. [cited 2020 Aug 09]. Available from: http://www.theses.fr/2018NORMR037.

Council of Science Editors:

Duflot T. Rôle de l'époxyde hydrolase soluble dans les maladies cardiovasculaires. : Role of soluble epoxide hydrolase in cardiovascular diseases. [Doctoral Dissertation]. Normandie; 2018. Available from: http://www.theses.fr/2018NORMR037


Tampere University

24. Rossi, Perttu. Eicosanoids and Lower Limb Ischemia .

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

 Väitöskirjassa arvioidaan lääkehoidon mahdollisuuksia jalan verenkiertohäiriöissä. Jalan menetyksiä (amputaatioita) pyritään estämään pallolaajennoksilla ja verisuonileikkauksilla, mutta lääkehoitoa on ollut niukasti tarjolla - yleensä käytössä on ollut… (more)

Subjects/Keywords: Eicosanoids and lower limb ischemia; Eikosanoidit ja jalan verenkiertohäiriöt

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APA (6th Edition):

Rossi, P. (2004). Eicosanoids and Lower Limb Ischemia . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/67414

Chicago Manual of Style (16th Edition):

Rossi, Perttu. “Eicosanoids and Lower Limb Ischemia .” 2004. Doctoral Dissertation, Tampere University. Accessed August 09, 2020. https://trepo.tuni.fi/handle/10024/67414.

MLA Handbook (7th Edition):

Rossi, Perttu. “Eicosanoids and Lower Limb Ischemia .” 2004. Web. 09 Aug 2020.

Vancouver:

Rossi P. Eicosanoids and Lower Limb Ischemia . [Internet] [Doctoral dissertation]. Tampere University; 2004. [cited 2020 Aug 09]. Available from: https://trepo.tuni.fi/handle/10024/67414.

Council of Science Editors:

Rossi P. Eicosanoids and Lower Limb Ischemia . [Doctoral Dissertation]. Tampere University; 2004. Available from: https://trepo.tuni.fi/handle/10024/67414


Michigan State University

25. Rieke, Caroline Jill. Studies involving the cyclooxygenase active sites of prostaglandin endoperoxide H synthase-1 and -2.

Degree: MS, Department of Biochemistry, 1999, Michigan State University

Subjects/Keywords: Arachidonic acid; Cyclooxygenases; Prostaglandins; Essential fatty acids; Eicosanoids

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APA (6th Edition):

Rieke, C. J. (1999). Studies involving the cyclooxygenase active sites of prostaglandin endoperoxide H synthase-1 and -2. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:28499

Chicago Manual of Style (16th Edition):

Rieke, Caroline Jill. “Studies involving the cyclooxygenase active sites of prostaglandin endoperoxide H synthase-1 and -2.” 1999. Masters Thesis, Michigan State University. Accessed August 09, 2020. http://etd.lib.msu.edu/islandora/object/etd:28499.

MLA Handbook (7th Edition):

Rieke, Caroline Jill. “Studies involving the cyclooxygenase active sites of prostaglandin endoperoxide H synthase-1 and -2.” 1999. Web. 09 Aug 2020.

Vancouver:

Rieke CJ. Studies involving the cyclooxygenase active sites of prostaglandin endoperoxide H synthase-1 and -2. [Internet] [Masters thesis]. Michigan State University; 1999. [cited 2020 Aug 09]. Available from: http://etd.lib.msu.edu/islandora/object/etd:28499.

Council of Science Editors:

Rieke CJ. Studies involving the cyclooxygenase active sites of prostaglandin endoperoxide H synthase-1 and -2. [Masters Thesis]. Michigan State University; 1999. Available from: http://etd.lib.msu.edu/islandora/object/etd:28499

26. Gautier-Veyret, Elodie. Rôle des eicosanoïdes dans l'athérogénèse associée au syndrome d'apnées obstructives du sommeil : approches clinique et expérimentale : Role of eicosanoids in atherogenesis related to obstructive sleep apnea : clinical and experimental approach.

Degree: Docteur es, Physiologie-Physiopathogie-Pharmacologie, 2016, Université Grenoble Alpes (ComUE)

Le syndrome d’apnées obstructives du sommeil (SAOS) affecte 5 à 20% de la population générale et est associée à des complications cardiovasculaires, ce qui en… (more)

Subjects/Keywords: Eicosanoïdes; Athérosclérose; Hypoxie intermittente; Syndrome d’apnées obstructives du sommeil; Eicosanoids; Atherosclerosis; Intermittent hypoxia; Obstructive sleep apnea; 570; 610

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APA (6th Edition):

Gautier-Veyret, E. (2016). Rôle des eicosanoïdes dans l'athérogénèse associée au syndrome d'apnées obstructives du sommeil : approches clinique et expérimentale : Role of eicosanoids in atherogenesis related to obstructive sleep apnea : clinical and experimental approach. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2016GREAV088

Chicago Manual of Style (16th Edition):

Gautier-Veyret, Elodie. “Rôle des eicosanoïdes dans l'athérogénèse associée au syndrome d'apnées obstructives du sommeil : approches clinique et expérimentale : Role of eicosanoids in atherogenesis related to obstructive sleep apnea : clinical and experimental approach.” 2016. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed August 09, 2020. http://www.theses.fr/2016GREAV088.

MLA Handbook (7th Edition):

Gautier-Veyret, Elodie. “Rôle des eicosanoïdes dans l'athérogénèse associée au syndrome d'apnées obstructives du sommeil : approches clinique et expérimentale : Role of eicosanoids in atherogenesis related to obstructive sleep apnea : clinical and experimental approach.” 2016. Web. 09 Aug 2020.

Vancouver:

Gautier-Veyret E. Rôle des eicosanoïdes dans l'athérogénèse associée au syndrome d'apnées obstructives du sommeil : approches clinique et expérimentale : Role of eicosanoids in atherogenesis related to obstructive sleep apnea : clinical and experimental approach. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2016. [cited 2020 Aug 09]. Available from: http://www.theses.fr/2016GREAV088.

Council of Science Editors:

Gautier-Veyret E. Rôle des eicosanoïdes dans l'athérogénèse associée au syndrome d'apnées obstructives du sommeil : approches clinique et expérimentale : Role of eicosanoids in atherogenesis related to obstructive sleep apnea : clinical and experimental approach. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2016. Available from: http://www.theses.fr/2016GREAV088


University of Vienna

27. Hagn, Gerhard. Evaluation of eicosanoid releasates in platelet concentrates consequent to two different pathogen inactivation techniques.

Degree: 2019, University of Vienna

Plättchen sind an einer Vielzahl von Prozessen im menschlichen Körper involviert, aber ihre wichtigste Rolle ist die Beteiligung an der Wundheilung. Die Lagerung von Plättchenkonzentraten… (more)

Subjects/Keywords: 35.23 Analytische Chemie: Allgemeines; 35.26 Massenspektrometrie; Eicosanoide / LC-MS / Plättchen / Pathogeninaktivierung; eicosanoids / LC-MS / platelets / pathogen inactivation

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

APA (6th Edition):

Hagn, G. (2019). Evaluation of eicosanoid releasates in platelet concentrates consequent to two different pathogen inactivation techniques. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/58338/

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):

Hagn, Gerhard. “Evaluation of eicosanoid releasates in platelet concentrates consequent to two different pathogen inactivation techniques.” 2019. Thesis, University of Vienna. Accessed August 09, 2020. http://othes.univie.ac.at/58338/.

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

MLA Handbook (7th Edition):

Hagn, Gerhard. “Evaluation of eicosanoid releasates in platelet concentrates consequent to two different pathogen inactivation techniques.” 2019. Web. 09 Aug 2020.

Vancouver:

Hagn G. Evaluation of eicosanoid releasates in platelet concentrates consequent to two different pathogen inactivation techniques. [Internet] [Thesis]. University of Vienna; 2019. [cited 2020 Aug 09]. Available from: http://othes.univie.ac.at/58338/.

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

Council of Science Editors:

Hagn G. Evaluation of eicosanoid releasates in platelet concentrates consequent to two different pathogen inactivation techniques. [Thesis]. University of Vienna; 2019. Available from: http://othes.univie.ac.at/58338/

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

28. Nelson, Jonathan W. Disruption of soluble epoxide hydrolase dimerization as a novel therapeutic target for stroke.

Degree: PhD, 2013, Oregon Health Sciences University

Subjects/Keywords: Epoxy compounds; Hydrolases; Peroxisomes; Ischemia; Eicosanoids; Proteins  – Physiological transport; Dimerization; Epoxide Hydrolases; Peroxisomes; Ischemia; Eicosanoids; Protein Transport

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

APA (6th Edition):

Nelson, J. W. (2013). Disruption of soluble epoxide hydrolase dimerization as a novel therapeutic target for stroke. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4N877SB ; http://digitalcommons.ohsu.edu/etd/885

Chicago Manual of Style (16th Edition):

Nelson, Jonathan W. “Disruption of soluble epoxide hydrolase dimerization as a novel therapeutic target for stroke.” 2013. Doctoral Dissertation, Oregon Health Sciences University. Accessed August 09, 2020. doi:10.6083/M4N877SB ; http://digitalcommons.ohsu.edu/etd/885.

MLA Handbook (7th Edition):

Nelson, Jonathan W. “Disruption of soluble epoxide hydrolase dimerization as a novel therapeutic target for stroke.” 2013. Web. 09 Aug 2020.

Vancouver:

Nelson JW. Disruption of soluble epoxide hydrolase dimerization as a novel therapeutic target for stroke. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 2013. [cited 2020 Aug 09]. Available from: doi:10.6083/M4N877SB ; http://digitalcommons.ohsu.edu/etd/885.

Council of Science Editors:

Nelson JW. Disruption of soluble epoxide hydrolase dimerization as a novel therapeutic target for stroke. [Doctoral Dissertation]. Oregon Health Sciences University; 2013. Available from: doi:10.6083/M4N877SB ; http://digitalcommons.ohsu.edu/etd/885


Universitat de Barcelona

29. Planagumà Ferrer, Anna. Efectes dels inhibidors de la ciclooxigenasa en cèl·lules hepàtiques i el seu paper en la inflamació i fibrosi hepàtica experimental.

Degree: Departament de Medicina, 2005, Universitat de Barcelona

 <i>The mechanism of action of aspirin (ASA) is related to cyclooxygenase (COX) inhibition, but additional actions cannot be excluded for their antiinflammatory and antithrombotic properties.… (more)

Subjects/Keywords: Prostaglandines; Aspirina; Eicosanoids; Fibrosi hepàtica; Inflamació crònica; Ciències de la Salut; 616

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

APA (6th Edition):

Planagumà Ferrer, A. (2005). Efectes dels inhibidors de la ciclooxigenasa en cèl·lules hepàtiques i el seu paper en la inflamació i fibrosi hepàtica experimental. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/2209

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):

Planagumà Ferrer, Anna. “Efectes dels inhibidors de la ciclooxigenasa en cèl·lules hepàtiques i el seu paper en la inflamació i fibrosi hepàtica experimental.” 2005. Thesis, Universitat de Barcelona. Accessed August 09, 2020. http://hdl.handle.net/10803/2209.

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

MLA Handbook (7th Edition):

Planagumà Ferrer, Anna. “Efectes dels inhibidors de la ciclooxigenasa en cèl·lules hepàtiques i el seu paper en la inflamació i fibrosi hepàtica experimental.” 2005. Web. 09 Aug 2020.

Vancouver:

Planagumà Ferrer A. Efectes dels inhibidors de la ciclooxigenasa en cèl·lules hepàtiques i el seu paper en la inflamació i fibrosi hepàtica experimental. [Internet] [Thesis]. Universitat de Barcelona; 2005. [cited 2020 Aug 09]. Available from: http://hdl.handle.net/10803/2209.

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

Council of Science Editors:

Planagumà Ferrer A. Efectes dels inhibidors de la ciclooxigenasa en cèl·lules hepàtiques i el seu paper en la inflamació i fibrosi hepàtica experimental. [Thesis]. Universitat de Barcelona; 2005. Available from: http://hdl.handle.net/10803/2209

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

30. Jouvène, Charlotte. Caractérisation de métabolites oxygénés dérivés des acides arachidonique et docosahexaénoïque dans le cerveau de rat : Characterization of oxygenated metabolites derived from arachidonic and docosahexaenoic acids in rat brain.

Degree: Docteur es, Biochimie, 2016, Lyon

Les acides docosahexaénoïque (DHA) et arachidonique (ArA), qui appartiennent respectivement aux familles n-3 et n-6, sont présents en grande quantité dans les tissus cérébraux, en… (more)

Subjects/Keywords: Acides gras polyinsaturés; Eicosanoïdes; Docosanoïdes; Cerveau; Lipoxygénases; Inflammation; UHPLC-MS/MS; Polyunsaturated fatty acids; Eicosanoids; Docosanoids; Brain; Lipoxygenases; Inflammation; UHPLC-MS/MS; 572

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

APA (6th Edition):

Jouvène, C. (2016). Caractérisation de métabolites oxygénés dérivés des acides arachidonique et docosahexaénoïque dans le cerveau de rat : Characterization of oxygenated metabolites derived from arachidonic and docosahexaenoic acids in rat brain. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSE1293

Chicago Manual of Style (16th Edition):

Jouvène, Charlotte. “Caractérisation de métabolites oxygénés dérivés des acides arachidonique et docosahexaénoïque dans le cerveau de rat : Characterization of oxygenated metabolites derived from arachidonic and docosahexaenoic acids in rat brain.” 2016. Doctoral Dissertation, Lyon. Accessed August 09, 2020. http://www.theses.fr/2016LYSE1293.

MLA Handbook (7th Edition):

Jouvène, Charlotte. “Caractérisation de métabolites oxygénés dérivés des acides arachidonique et docosahexaénoïque dans le cerveau de rat : Characterization of oxygenated metabolites derived from arachidonic and docosahexaenoic acids in rat brain.” 2016. Web. 09 Aug 2020.

Vancouver:

Jouvène C. Caractérisation de métabolites oxygénés dérivés des acides arachidonique et docosahexaénoïque dans le cerveau de rat : Characterization of oxygenated metabolites derived from arachidonic and docosahexaenoic acids in rat brain. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2020 Aug 09]. Available from: http://www.theses.fr/2016LYSE1293.

Council of Science Editors:

Jouvène C. Caractérisation de métabolites oxygénés dérivés des acides arachidonique et docosahexaénoïque dans le cerveau de rat : Characterization of oxygenated metabolites derived from arachidonic and docosahexaenoic acids in rat brain. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSE1293

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