Auswahl der wissenschaftlichen Literatur zum Thema „Metabolism of cholesterol derivatives“
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Zeitschriftenartikel zum Thema "Metabolism of cholesterol derivatives"
Zhao, Chunyan, und Karin Dahlman-Wright. „Liver X receptor in cholesterol metabolism“. Journal of Endocrinology 204, Nr. 3 (16.10.2009): 233–40. http://dx.doi.org/10.1677/joe-09-0271.
Der volle Inhalt der QuelleReboldi, Andrea, und Eric Dang. „Cholesterol metabolism in innate and adaptive response“. F1000Research 7 (16.10.2018): 1647. http://dx.doi.org/10.12688/f1000research.15500.1.
Der volle Inhalt der QuelleBilai, I. M., M. I. Romanenko und D. H. Ivanchenko. „Study on the influence of 7-β-hydroxy-γ-aryloxypropylxanthinyl-8-thioalkanic acid derivatives on the lipid metabolism in experiment“. Zaporozhye Medical Journal 23, Nr. 3 (07.06.2021): 411–16. http://dx.doi.org/10.14739/2310-1210.2021.3.207465.
Der volle Inhalt der QuelleNunomura, Satoshi, Makoto Makishima und Chisei Ra. „Liver X receptors and immune regulation“. BioMolecular Concepts 1, Nr. 5-6 (01.12.2010): 381–87. http://dx.doi.org/10.1515/bmc.2010.030.
Der volle Inhalt der QuellePirmoradi, Leila, Nayer Seyfizadeh, Saeid Ghavami, Amir A. Zeki und Shahla Shojaei. „Targeting cholesterol metabolism in glioblastoma: a new therapeutic approach in cancer therapy“. Journal of Investigative Medicine 67, Nr. 4 (14.02.2019): 715–19. http://dx.doi.org/10.1136/jim-2018-000962.
Der volle Inhalt der QuelleRoth, Andrew T., Jennifer A. Philips und Pallavi Chandra. „The role of cholesterol and its oxidation products in tuberculosis pathogenesis“. Immunometabolism 6, Nr. 2 (April 2024): e00042. http://dx.doi.org/10.1097/in9.0000000000000042.
Der volle Inhalt der QuelleKarolczak, Kamil, und Cezary Watala. „The Mystery behind the Pineal Gland: Melatonin Affects the Metabolism of Cholesterol“. Oxidative Medicine and Cellular Longevity 2019 (10.07.2019): 1–8. http://dx.doi.org/10.1155/2019/4531865.
Der volle Inhalt der QuelleSHAND, JOHN H., und DAVID W. WEST. „The effect of fibric acid derivatives on cholesterol metabolism in rat liver“. Biochemical Society Transactions 22, Nr. 2 (01.05.1994): 110S. http://dx.doi.org/10.1042/bst022110s.
Der volle Inhalt der QuelleSchroepfer, George J. „Oxysterols: Modulators of Cholesterol Metabolism and Other Processes“. Physiological Reviews 80, Nr. 1 (01.01.2000): 361–554. http://dx.doi.org/10.1152/physrev.2000.80.1.361.
Der volle Inhalt der QuelleGylling, Helena, und Tatu A. Miettinen. „The effect of plant stanol- and sterol-enriched foods on lipid metabolism, serum lipids and coronary heart disease“. Annals of Clinical Biochemistry: International Journal of Laboratory Medicine 42, Nr. 4 (01.07.2005): 254–63. http://dx.doi.org/10.1258/0004563054255605.
Der volle Inhalt der QuelleDissertationen zum Thema "Metabolism of cholesterol derivatives"
Norlin, Maria. „Cytochrome P450 Enzymes in the Metabolism of Cholesterol and Cholesterol Derivatives“. Doctoral thesis, Uppsala University, Department of Pharmaceutical Biosciences, 2000. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1086.
Der volle Inhalt der QuelleCholesterol is metabolized to a variety of important biological products in the body including bile acids and vitamin D. The present investigation is focused on enzymes that catalyze 7α-hydroxylation or 27-hydroxylation in the metabolism of cholesterol, oxysterols (side chain-hydroxylated derivatives of cholesterol) and vitamin D3. The enzymes studied belong to the cytochrome P450 enzyme families CYP7 and CYP27.
The study describes purification of a cytochrome P450 enzyme fraction active in 7α-hydroxylation of 25-hydroxycholesterol, 27-hydroxycholesterol, dehydroepiandrosterone and pregnenolone from pig liver microsomes. Peptide sequence analysis indicated that this enzyme fraction contains an enzyme belonging to the CYP7B subfamily. The purified enzyme was not active towards cholesterol or testosterone. Purification and inhibition experiments suggested that hepatic microsomal 7α -hydroxylation of 27-hydroxycholesterol and dehydroepiandrosterone involves at least two enzymes, probably closely related.
The study shows that recombinantly expressed human and rat cholesterol 7α -hydroxylase (CYP7A) and partially purified pig liver cholesterol 7α -hydroxylase are active towards 20(S)-, 24-, 25- and 27-hydroxycholesterol. CYP7A was previously considered specific for cholesterol and cholestanol. The 7α -hydroxylation of 20(S)-, 25-, and 27-hydroxycholesterol in rat liver was significantly increased by treatment with cholestyramine, an inducer of CYP7A. Cytochrome P450 of renal origin showed 7α -hydroxylase activity towards 25- and 27-hydroxycholesterol, dehydroepiaundrosterone and pregnenolone but not towards 20(S)-, 24-hydroxycholesterol or cholesterol. The results indicate a physiological role for CYP7A as an oxysterol 7α -hydroxylase, in addition to the previously known human oxysterol 7α -hydroxylase CYP7B.
The role of renal sterol 27-hydroxylase (CYP27A) in the bioactivation of vitamin D3 was studied with cytochrome P450 fractions purified from pig kidney mitochondria. Purification and inhibition experiments and experiments with a monoclonal antibody against CYP27A indicated that CYP27A plays a role in renal 25-hydroxyvitamin D3 l α -hydroxylation.
The expression of CYP7A, CYP7B and CYP27A during development was studied. The levels of CYP27A in livers of newborn and six months old pigs were similar whereas the levels of CYP7A increased. The expression of CYP7B varied depending on the tissue. The expression of CYP7B increased with age in the liver whereas the CYP7B levels in kidney showed a marked age-dependent decrease.
Patel, Dilipkumar. „Cholesterol metabolism in monocyte-derived macrophages“. Thesis, Imperial College London, 1990. http://hdl.handle.net/10044/1/46492.
Der volle Inhalt der QuelleHoang, Van Quyen. „Cholesterol metabolism in cultured hamster hepatocytes“. Thesis, Royal Veterinary College (University of London), 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.522583.
Der volle Inhalt der Quelle曾紹怡 und Siu-yee Patricia Tsang. „Regulation of cholesterol metabolism in hepatocytes“. Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2000. http://hub.hku.hk/bib/B31969835.
Der volle Inhalt der QuelleSimonen, Piia. „Cholesterol metabolism in type 2 diabetes“. Helsinki : University of Helsinki, 2002. http://ethesis.helsinki.fi/julkaisut/laa/kliin/vk/simonen/.
Der volle Inhalt der QuelleTsang, Siu-yee Patricia. „Regulation of cholesterol metabolism in hepatocytes“. Hong Kong : University of Hong Kong, 2000. http://sunzi.lib.hku.hk/hkuto/record.jsp?B22032459.
Der volle Inhalt der QuelleBoone, Lindsey R. „Thyroid Hormone Regulation of Cholesterol Metabolism“. [Tampa, Fla] : University of South Florida, 2009. http://purl.fcla.edu/usf/dc/et/SFE0003089.
Der volle Inhalt der QuelleSampson, William James. „The intracellular control of cholesterol metabolism“. Thesis, University of Edinburgh, 1988. http://hdl.handle.net/1842/26913.
Der volle Inhalt der QuelleJiang, Zhao-Yan. „Studies on cholesterol and bile acid metabolism in Chinese cholesterol gallstone patients“. Stockholm, 2010. http://diss.kib.ki.se/2010/978-91-7409-844-0/.
Der volle Inhalt der QuelleSkogsberg, Josefin. „PPAR delta : its role in cholesterol metabolism /“. Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-604-9.
Der volle Inhalt der QuelleBücher zum Thema "Metabolism of cholesterol derivatives"
Sabine, John R. Cholesterol. Ann Arbor, Mich: University Microfilms International, 1992.
Den vollen Inhalt der Quelle findenLupovici, Zaharia. Good cholesterol, bad cholesterol, and the most discussed cholesterol-- HDL. New York: Vantage Press, 1992.
Den vollen Inhalt der Quelle findenPhilip, Yeagle, Hrsg. Biology of cholesterol. Boca Raton, Fla: CRC Press, 1988.
Den vollen Inhalt der Quelle finden1939-, Esfahani Mojtaba, und Swaney John B. 1944-, Hrsg. Advances in cholesterol research. Caldwell, N.J: Telford Press, 1990.
Den vollen Inhalt der Quelle findenSymposium on Lipoprotein and Cholesterol Metabolism in Steroidogenic Tissues (1984 Laval University). Lipoprotein and cholesterol metabolism in steroidogenic tissues. Philadelphia: Georg F. Stickley Co., 1985.
Den vollen Inhalt der Quelle findenPearce, Jack B. Dietary dairy products and mammalian cholesterol metabolism. Belfast: Food and Agricultural Chemistry Department, Queen's University of Belfast, 1989.
Den vollen Inhalt der Quelle findenMyant, N. B. Cholesterol metabolism, LDL, and the LDL receptor. San Diego: Academic Press, 1990.
Den vollen Inhalt der Quelle finden1947-, Strauss Jerome F., und Menon K. M. J, Hrsg. Lipoprotein and cholesterol metabolism in steroidogenic tissues. Philadelphia: G. F. STickley, 1985.
Den vollen Inhalt der Quelle findenY, Chang T., und Freeman Dale A, Hrsg. Intracellular cholesterol trafficking. Boston: Kluwer Academic Publishers, 1998.
Den vollen Inhalt der Quelle findenShi-Kaung, Peng, und Morin Robert J, Hrsg. Biological effects of cholesterol oxides. Boca Raton: CRC Press, 1992.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Metabolism of cholesterol derivatives"
Van Berkel, Theo J. C., Helene Vietsch und Erik A. L. Biessen. „Lowering of Serum Cholesterol Levels by a Cholesterol Derivative of a New Triantennary Cluster Galactoside“. In Drugs Affecting Lipid Metabolism, 531–39. Dordrecht: Springer Netherlands, 1996. http://dx.doi.org/10.1007/978-94-009-0311-1_62.
Der volle Inhalt der QuelleMøller, Jens. „Free Fatty Acid Metabolism“. In Cholesterol, 8. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_5.
Der volle Inhalt der QuelleHowles, Philip N., und David Y. Hui. „Cholesterol Esterase“. In Intestinal Lipid Metabolism, 119–34. Boston, MA: Springer US, 2001. http://dx.doi.org/10.1007/978-1-4615-1195-3_7.
Der volle Inhalt der QuelleWüstner, Daniel. „Intracellular Cholesterol Transport“. In Cellular Lipid Metabolism, 157–90. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-00300-4_6.
Der volle Inhalt der QuelleSteinberg, D. „Transport of Cholesterol and Cholesterol Esters by HDL“. In Drugs Affecting Lipid Metabolism, 42–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71702-4_7.
Der volle Inhalt der QuelleHowles, Philip N. „Cholesterol Absorption and Metabolism“. In Methods in Molecular Biology, 157–79. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60761-058-8_10.
Der volle Inhalt der QuelleHowles, Philip N. „Cholesterol Absorption and Metabolism“. In Methods in Molecular Biology, 177–97. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3661-8_11.
Der volle Inhalt der QuelleMc Auley, Mark T. „Aging and Cholesterol Metabolism“. In Encyclopedia of Gerontology and Population Aging, 1–6. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-69892-2_122-1.
Der volle Inhalt der QuelleMc Auley, Mark T. „Aging and Cholesterol Metabolism“. In Encyclopedia of Gerontology and Population Aging, 220–25. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-22009-9_122.
Der volle Inhalt der QuelleMarinetti, Guido V. „Disorders of Cholesterol Metabolism“. In Disorders of Lipid Metabolism, 63–74. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-9564-9_5.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Metabolism of cholesterol derivatives"
Jovanović-Šanta, Suzana S., Aleksandar M. Oklješa, Antos B. Sachanka, Yaraslau U. Dzichenka und Sergei A. Usanov. „17-SUBSTITUTED STEROIDAL TETRAZOLES – NOVEL LIGANDS FOR HUMAN STEROID-CONVERTING CYP ENZYMES“. In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.336js.
Der volle Inhalt der QuelleYang, L., Q. Yang, Q. H. Liu, H. Zhang, S. H. Sun und T. C. Zhuang. „Rice protein level affects cholesterol metabolism“. In EM 2011). IEEE, 2011. http://dx.doi.org/10.1109/icieem.2011.6035585.
Der volle Inhalt der QuelleStopsack, Konrad H., Travis A. Gerke, Lorelei A. Mucci und Jennifer R. Rider. „Abstract 60: PTEN expression, cholesterol metabolism, and lethal prostate cancer“. In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-60.
Der volle Inhalt der QuelleHe, Sisi, Georgina Cheng, Edward Roy, Marta Spain, Ronald Kimball, Nikolas Snyder, Melina Salgado et al. „Abstract 2821: Cholesterol and its metabolism impact ovarian cancer progression“. In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-2821.
Der volle Inhalt der QuelleYue, Shuhua, Junjie Li, Seung Young Lee, Tian Shao, Bing Song, Liang Cheng, Chang-Deng Hu, Xiaoqi Liu, Timothy L. Ratliff und Ji-Xin Cheng. „Abstract 1893: Spectroscopic imaging unveils altered cholesterol metabolism in prostate cancer .“ In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-1893.
Der volle Inhalt der QuelleLudescher, M., N. Stamm, T. Fehm und H. Neubauer. „PGRMC1 interacts with proteins of the cholesterol synthesis pathway resulting in altered cholesterol metabolism in breast cancer cells“. In Abstracts of the 10th Scientific Symposium of the Comission for Translational Research of the Working group for Gynecologic Oncology AGO e.V. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1675447.
Der volle Inhalt der QuelleYoda, Tsuyoshi, Huong Phan Thi Thanh, Mun'delanji C. Vestergaard, Tsutomu Hamada und Masahiro Takagi. „Thermo-induced dynamics of membranes and liquid crystals containing cholesterol derivatives“. In 2012 International Symposium on Micro-NanoMechatronics and Human Science (MHS). IEEE, 2012. http://dx.doi.org/10.1109/mhs.2012.6492459.
Der volle Inhalt der QuelleWang, Sai, Frederik Link, Mei Han, Roohi Chaudhary, Anastasia Asimakopoulos, Roman Liebe, Ye Yao et al. „Reciprocal Inhibitory Regulation of TGF-β1 Signaling and Cholesterol Metabolism in Hepatocytes“. In 40. Jahrestagung der Deutschen Arbeitsgemeinschaft zum Studium der Leber. Georg Thieme Verlag, 2024. http://dx.doi.org/10.1055/s-0043-1777574.
Der volle Inhalt der QuelleVerbrugghe, Adronie, und Alexandra Rankovic. „Dietary choline in feline nutrition and its role in obesity prevention and liver health“. In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/gyun6061.
Der volle Inhalt der QuelleMuth, Aaron, Veethika Pandey, Xianlin Han, Deborah Altomare und Otto Phanstiel. „Abstract A108: Targeting sphingolipid metabolism and metastasis with motuporamine derivatives“. In Abstracts: AACR Special Conference on Pancreatic Cancer: Innovations in Research and Treatment; May 18-21, 2014; New Orleans, LA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.panca2014-a108.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Metabolism of cholesterol derivatives"
Min, Byungrok, Il Suk Kim und Dong U. Ahn. Dietary Cholesterol Affects Lipid Metabolism in Rabbits. Ames (Iowa): Iowa State University, Januar 2015. http://dx.doi.org/10.31274/ans_air-180814-1348.
Der volle Inhalt der QuelleHung, Hsuan-Yu, Hui-Hsiung Lai, Hui-Chuan Lin und Chung-Yu Chen. Impact of interferon-free antivirus therapy on lipid profiles in patients with chronic hepatitis C: A network meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, Juli 2022. http://dx.doi.org/10.37766/inplasy2022.7.0055.
Der volle Inhalt der QuelleGao, Hui, Chen Gong, Shi-chun Shen, Jia-ying Zhao, Dou-dou Xu, Fang-biao Tao, Yang Wang und Xiao-chen Fan. A systematic review on the associations between prenatal phthalate exposure and childhood glycolipid metabolism and blood pressure: evidence from epidemiological studies. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, Juni 2022. http://dx.doi.org/10.37766/inplasy2022.6.0111.
Der volle Inhalt der Quelleyu, luyou, jinping yang, xi meng und yanhua lin. Effectiveness of the gut microbiota-bile acid pathway (BAS) in the treatment of Type 2 diabetes: A protocol for systematic review and meta analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, Juli 2022. http://dx.doi.org/10.37766/inplasy2022.7.0117.
Der volle Inhalt der QuelleMeidan, Rina, und Robert Milvae. Regulation of Bovine Corpus Luteum Function. United States Department of Agriculture, März 1995. http://dx.doi.org/10.32747/1995.7604935.bard.
Der volle Inhalt der QuelleJander, Georg, und Daniel Chamovitz. Investigation of growth regulation by maize benzoxazinoid breakdown products. United States Department of Agriculture, Januar 2015. http://dx.doi.org/10.32747/2015.7600031.bard.
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