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Artykuły w czasopismach na temat "Cholesterol"

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Liang, Congxin, Liqun Yan, J�rg-R. Hill, Carl S. Ewig, Terry R. Stouch, and Arnold T. Hagler. "Force field studies of cholesterol and cholesteryl acetate crystals and cholesterol-cholesterol intermolecular interactions." Journal of Computational Chemistry 16, no. 7 (1995): 883–97. http://dx.doi.org/10.1002/jcc.540160706.

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Vill, V., J. Thiem, and P. Rollin. "Flüssigkristalline aromatische Cholesterin-Derivate." Zeitschrift für Naturforschung A 47, no. 3 (1992): 515–20. http://dx.doi.org/10.1515/zna-1992-0313.

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Abstract Liquid Crystalline Aromatic Cholesterol Derivates A series of aromatic cholesteryl ethers, esters, phenylcarbonates and benzylcarbonates were prepared and their liquid crystalline properties studied. The occurence of ferroelectric phases as well as properties of cholesteric and blue phases alternate with the number of linking atomes between steroid and atomatic system
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Robins, S. J., J. M. Fasulo, C. R. Pritzker, J. M. Ordovas, and G. M. Patton. "Diurnal changes and adaptation by the liver of hamsters to an atherogenic diet." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 269, no. 6 (1995): R1327—R1332. http://dx.doi.org/10.1152/ajpregu.1995.269.6.r1327.

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Studies were performed in freely feeding, male (F1B) Syrian hamsters fed a high-fat diet to determine the extent and manner of adaptation of the liver to diurnal changes in eating patterns and an increase in serum lipids. Serum cholesterol and triglycerides strongly paralleled changes in food consumption and were 40-50% greater during the 12-h dark period than the 12-h light period of the diurnal cycle. Hepatic cholesterol changes closely approximated changes in serum cholesterol (r = 0.916) due principally to changes in hepatic cholesteryl esters that were on average about 10-fold greater wit
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Khan, B., H. G. Wilcox, and M. Heimberg. "Cholesterol is required for secretion of very-low-density lipoprotein by rat liver." Biochemical Journal 258, no. 3 (1989): 807–16. http://dx.doi.org/10.1042/bj2580807.

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To study potential effects of hepatic cholesterol concentration on secretion of very-low-density lipoprotein (VLDL) by the liver, male rats were fed on unsupplemented chow, chow with lovastatin (0.1%), or chow with lovastatin (0.1%) and cholesterol (0.1%) for 1 week. Livers were isolated from these animals and perfused in vitro, with a medium containing [2-14C]acetate, bovine serum albumin and glucose in Krebs-Henseleit buffer, and with an oleate-albumin complex. With lovastatin feeding, the hepatic concentrations of cholesteryl esters and triacylglycerols before perfusion were decreased, alth
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Gylling, H., S. Pyrhönen, E. Mäntylä, H. Mäenpää, L. Kangas, and T. A. Miettinen. "Tamoxifen and toremifene lower serum cholesterol by inhibition of delta 8-cholesterol conversion to lathosterol in women with breast cancer." Journal of Clinical Oncology 13, no. 12 (1995): 2900–2905. http://dx.doi.org/10.1200/jco.1995.13.12.2900.

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PURPOSE Long-term effects of tamoxifen and toremifene, a new antiestrogen that closely resembles tamoxifen, were investigated on serum lipids and cholesterol metabolism. PATIENTS AND METHODS The study group consisted of 24 postmenopausal Finnish women with advanced breast cancer from an international multicenter study of 415 patients. Cholesterol metabolism was evaluated by measuring the cholesterol precursor (delta 8-cholestenol, desmosterol, and lathosterol, reflecting cholesterol synthesis) and plant sterol (markers of cholesterol absorption) and cholestanol levels by gas-liquid chromatogra
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Scobey, M. W., F. L. Johnson, and L. L. Rudel. "Delivery of high-density lipoprotein free and esterified cholesterol to bile by the perfused monkey liver." American Journal of Physiology-Gastrointestinal and Liver Physiology 257, no. 4 (1989): G644—G652. http://dx.doi.org/10.1152/ajpgi.1989.257.4.g644.

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The movement of cholesterol from high-density lipoproteins (HDL) into bile has been studied using perfused livers from cholesterol-fed African Green monkeys. Mass amounts of HDL were isolated from the plasma of African Green monkeys and were doubly labeled with either 125I-apolipoprotein and [3H]cholesteryl ester or with [3H]cholesteryl ester and [14C]cholesterol. For 3 h of perfusion HDL-free cholesterol was cleared from perfusate at a faster rate than HDL ester cholesterol which, in turn, was cleared at a faster rate than HDL protein. [14C]cholesterol from HDL appeared in biliary bile acids
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Rodriguez-Agudo, Daniel, Shunlin Ren, Eric Wong, et al. "Intracellular cholesterol transporter StarD4 binds free cholesterol and increases cholesteryl ester formation." Journal of Lipid Research 49, no. 7 (2008): 1409–19. http://dx.doi.org/10.1194/jlr.m700537-jlr200.

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Lystvan, V., A. Zhmurchuk, and V. Lystvan. "SYNTHESIS OF POTENTIAL LIQUID CRYSTALS WITH CHOLESTEROL FRAGMENT BY WITTIG REACTION." Ukrainian Journal of Natural Sciences, no. 2 (January 28, 2023): 143–54. http://dx.doi.org/10.35433/naturaljournal.2.2023.144-154.

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Liquid crystals are substances that owing to the features of their structure and physical properties are of interest not only as objects for theoretical research, but also significantly important practically due to the possibilities of their effective application in various brunches of industry, medicine, in household etc. Among the known classes of liquid crystals, substances known as cholesterics are an important group.
 Cholesteric liquid crystals demonstrate very high optical activity, that significantly exceeds the optical activity of most other known classes of organic compounds. Th
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Hallikainen, Maarit, Henri Tuomilehto, Tarja Martikainen, et al. "Cholesterol Metabolism and Weight Reduction in Subjects with Mild Obstructive Sleep Apnoea: A Randomised, Controlled Study." Cholesterol 2013 (May 16, 2013): 1–9. http://dx.doi.org/10.1155/2013/769457.

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To evaluate whether parameters of obstructive sleep apnoea (OSA) associate with cholesterol metabolism before and after weight reduction, 42 middle-aged overweight subjects with mild OSA were randomised to intensive lifestyle intervention (N=23) or to control group (N=18) with routine lifestyle counselling only. Cholesterol metabolism was evaluated with serum noncholesterol sterol ratios to cholesterol, surrogate markers of cholesterol absorption (cholestanol and plant sterols) and synthesis (cholestenol, desmosterol, and lathosterol) at baseline and after 1-year intervention. At baseline, art
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Mayorek, N., та J. Bar-Tana. "Hypocholesterolaemic effect of β β'-methyl-substituted hexadecanedioic acid (MEDICA 16) in the male hamster". Biochemical Journal 289, № 3 (1993): 911–17. http://dx.doi.org/10.1042/bj2890911.

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Treatment of cholesterol-fed male hamsters kept on a diet of purina chow with beta beta'-methyl-substituted hexadecanedioic acid (MEDICA 16) resulted in a progressive hypocholesterolaemic effect, amounting to a 50% decrease in the cholesterol content of all plasma lipoproteins. The decrease in plasma cholesterol could be accounted for by activation of plasma-cholesterol efflux through the liver into the bile mediated by MEDICA 16-induced (a) increase of the number of liver LDL receptors, (b) activation of liver neutral cholesteryl ester hydrolase with a concomitant inhibition of liver acyl-CoA
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Rozprawy doktorskie na temat "Cholesterol"

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Edington, J. "The relationship of dietary cholesterol to plasma cholesteroll." Thesis, University of Oxford, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236284.

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Malcolmson, Richard Joseph. "Physical studies of cholesterol and cholesteryl esters in model membranes." Thesis, Edinburgh Napier University, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.385910.

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Velarde, Laos Edmundo, and Ana Gonzalez. "Cholesterol and Cholesterol Oxides in Chicken Meat." Revista de Química, 2012. http://repositorio.pucp.edu.pe/index/handle/123456789/99119.

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Se determinó el contenido de lípidos totales, colesterol yóxidos de colesterol en carne de pollo adquiridos en 3avícolas de Lima. La carne de pollo presentó valores de lípidostotales y colesterol diferentes porpresentó los menores valores demientras que la piel presentó losavícola. La carne de pecholípidos totales y colesterol,mayores valores de estos. Por cromatografía de gases acoplado a espectrómetro demasas (CG-EM) se confirmó la estructura de los siguientes óxidosde colesterol: 7-cetocolesterol, en las 3 avícolas; 7 β -hidroxicolesterol en ala de la avícola 1 y piel de la avícola 2; 7 -hi
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Kingdon, Lorraine B. "Speedy Cholesterol." College of Agriculture, University of Arizona (Tucson, AZ), 1990. http://hdl.handle.net/10150/295659.

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Famer, Daniel. "Implications of cholesterol and cholesterol-lowering therapy in Alzheimer's disease /." Stockholm, 2007. http://diss.kib.ki.se/2007/978-91-7357-260-6/.

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Burkett, Paul A. "Frequent cholesterol feedback as an aid in lowering cholesterol levels." Thesis, Virginia Tech, 1989. http://hdl.handle.net/10919/44704.

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Twenty six male and two female participants in the Cardiac Therapy Program at Virginia Tech were stratified, based upon level of total cholesterol (TC) and length of time in the Cardiac Program, and then randomly assigned to either experimental or control groups. Participants ranged in age from 43 to 68 years and all had baseline TC levels greater than 200 mg/dl. There were no significant differences between groups in terms of baseline TC (control M : 248 mg/dl; experimental M = 251 mg/dl), blood pressure (BP), weight, predicted percent body fat, dietary fat/cholesterol, age, education, or
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Alasmi, Mahmood Mohamed. "EFFECTS OF CHOLESTEROL SUPPLEMENTATION ON CHOLESTEROL SYNTHESIS RATES IN INFANTS." University of Cincinnati / OhioLINK, 2000. http://rave.ohiolink.edu/etdc/view?acc_num=ucin974741712.

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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.

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<p>Cholesterol 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 D<sub>3</sub>. The enzymes studied belong to the cytochrome P450 enzyme families CYP7 and CYP27.</p><p>The study describes purification of a cytochrome P450 enzyme fraction active in 7α-hydroxylation of 25-hydroxycholesterol, 27-hydroxycholesterol, dehydroepiandroste
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Trevenen, Alexandra H. "Investigations of phospholipid/cholesterol and cholesterol derivative interactions in model membranes." Thesis, Imperial College London, 2010. http://hdl.handle.net/10044/1/5582.

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Multinuclear solid state MAS NMR (1H and 31P), 31P CSA solid state NMR, 2H NMR and x-ray diffraction techniques have been used to compare the structure and properties of DPPC: Andro and DPPC: 4β-hydroxycholesterol with that of the properties known of DPPC: Chol mixtures in excess water. The formation of the Lo phase is known to occur with PC: Chol mixtures with sufficient concentrations of cholesterol. The formation and properties of the Lo phase was looked at with the cholesterol derivatives Andro (lacking in the hydrocarbon tail present in cholesterol) and 4β-hydroxycholesterol (possessing a
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Beehler, Kaitlyn. "MiR-1908 Is a Cholesterol Responsive MicroRNA Implicated In Cholesterol Regulation." Thesis, Université d'Ottawa / University of Ottawa, 2020. http://hdl.handle.net/10393/40422.

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Leveraging miRNA-Seq data and the 1000 Genomes imputed genotypes, we identified rs174561-C as a strong miRQTL for circulating miRNA-1908-5p (P=4.8x10-31) which has an inverse relationship with circulating LDL-C, fasting glucose and A1c. Here I investigated the molecular mechanism(s) linking miR1908-5p to cholesterol metabolism. First, by overexpression experiments in HuH-7 cells demonstrate that the presence of the C allele, associated with lower LDL-C levels, significantly increases miR-1908-5p by 2.15-fold relative to the T allele. Further experiments revealed that 72-hour cholesterol deplet
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Książki na temat "Cholesterol"

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Roth, Eli. Good cholesterol, bad cholesterol. 2nd ed. Prima Pub., 1995.

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Roth, Eli. Good cholesterol, bad cholesterol. Prima Pub. & Communications, 1988.

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Roth, Eli. Good cholesterol, bad cholesterol. Prima Pub. & Communications, 1988.

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A, Kramer M., ed. Cholesterol. Nova Science Publishers, 2005.

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Møller, Jens. Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3.

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Daninos, Jean-Michel. Cholesterol. W.A.B., 1995.

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Carole, Michaud, ed. Cholesterol. Modus Vivendi, 2014.

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Sabine, John R. Cholesterol. University Microfilms International, 1992.

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G, Williams David. Cholesterol. Mountain Home Pub., 1988.

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Lupovici, Zaharia. Good cholesterol, bad cholesterol, and the most discussed cholesterol-- HDL. Vantage Press, 1992.

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Części książek na temat "Cholesterol"

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Møller, Jens. "Cholesterol." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_1.

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Møller, Jens. "Infarction Due to Metabolic Processes Other than Vessel Occlusion." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_10.

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Møller, Jens. "Testosterone as an Alternative to Surgery for CVD." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_11.

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Møller, Jens. "Diabetic States and CVD." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_12.

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Møller, Jens. "Use of Anabolic Steroids in Surgical Stress." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_13.

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Møller, Jens. "Increasing Testosterone and Decreasing Cholesterol by Physical Training." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_14.

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Møller, Jens. "The Negative Nitrogen Balance." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_15.

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Møller, Jens. "Evaluation of the Parameters of CVD." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_16.

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Møller, Jens. "Comments on Photographs." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_17.

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Møller, Jens. "The Balance Between Hormone Sensitive Lipase and Postheparin Lipoprotein Lipase." In Cholesterol. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-71600-3_18.

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Streszczenia konferencji na temat "Cholesterol"

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Halim, Erwin, Steven, Aurellia Nurfadhila Sembada Putri, Davine Dorothy Halim, and Dedy Syamsuar. "Utilizing Digital Information for Personalized Cholesterol Management." In 2024 Ninth International Conference on Informatics and Computing (ICIC). IEEE, 2024. https://doi.org/10.1109/icic64337.2024.10956936.

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Maram, Balajee, Gotte Vasavi, V. Vasudha Rani, B. Ramesh, M. Narendra Nadh Reddy, and Sasibhushana Rao Pappu. "Predictive Models of Cholesterol Levels through Protein Expression Patterns." In 2024 International Conference on Intelligent Systems and Advanced Applications (ICISAA). IEEE, 2024. https://doi.org/10.1109/icisaa62385.2024.10829210.

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Pescador, R., R. Porta, R. Niada, M. Mantovani, and G. Prino. "DEFIBROTIDE DECREASES CHOLESTEROL CONTENT IN HYPERCHOLESTEROLEMIC RABBIT AORTA, WITH NO MODIFICATION OF PLASMA OR LIPOPROTEIN CHOLESTEROL." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643153.

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Defibrotide was shown to stimulate the production of endogenous PGI2 from rat and hamster aortic tissue, as well as the production of PGi2 frcm the coronary vascular bed in the platelet perfused heart model. This effect was only seen in presence of platelets. Durirg the infusion period with Defibrotide thromboxane release remained unaffected while platelet cAMP rised. Defibrotide, was also able to reduce the secretion of ATP from platelets as well as to deaggregate platelet cluTps. It has been postulated that long-term administration of stable PGI^ metabolites or analogues could be a more usef
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Perdani, Meka Saima, Muhamad Sahlan, Siti Farida, Dwini Normayulisa Putri, Sri Angky Soekanto, and Heri Hermansyah. "Kinetic study of cholesterol oxidation by cholesterol oxidase enzyme as application for cholesterol biosensor." In SECOND INTERNATIONAL CONFERENCE OF MATHEMATICS (SICME2019). Author(s), 2019. http://dx.doi.org/10.1063/1.5096731.

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Heiremans, J., M. Claeys, and A. G. Herman. "DETERMINATION OF CHOLESTERYL HYDROXYOCTADBCADIENOATES IN VASCULAR TISSUE BY HPLC AND ITS RELEVANCE TO ATHEROSCLEROSIS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643084.

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Accumulation of lipids in the intimal arterial layer, and of cholesterol esters in particular, has been recognised as an early and prominent phenomenon in atherogenesis. Several attempts have been made to link putative peroxidation of these lipids in vivo to causal or deteriorating etiological determinants of plaque formation. The occurrence in advanced human atheromata of oxidized derivatives of cholesteryl linoleate -a major polyunsaturated cholesterol ester species in plasma and vessel wall - has been described by Brooks et al. (Atherosclerosis, 1970,13,223) and a positive correlation betwe
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Zhang, Peipei, Jun Huang, Mengshi Li, Pengfei Zhang, and Liyun Ding. "A fiber optic cholesterol biosensor based on magnetic immobilized cholesterol oxidase." In Asia-Pacific Optical Sensors Conference. OSA, 2016. http://dx.doi.org/10.1364/apos.2016.w4a.59.

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Ghelmez, Mihaela A., Maria Honciuc, and Cristian Gheorghe. "Estimation of the cholesterol percentages in mixtures of arachidonic acid and cholesterol." In OE/LASE '94, edited by Joseph R. Lakowicz. SPIE, 1994. http://dx.doi.org/10.1117/12.182774.

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Kokal, Sunil L., and Selim G. Sayegh. "Asphaltenes: The Cholesterol Of Petroleum." In Middle East Oil Show. Society of Petroleum Engineers, 1995. http://dx.doi.org/10.2118/29787-ms.

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Rathinam, R., Devesh Pratap Singh, Arjun Dutta, S. Rudresha, Shaikh Rajesh Ali, and Pratik Chatterjee. "TiO<sub>2</sub> Nanoparticles Based Peroxidase Mimics for Colorimetric Sensing of Cholesterol and Hydrogen Peroxide." In International Conference on Recent Advancements in Biomedical Engineering. Trans Tech Publications Ltd, 2022. http://dx.doi.org/10.4028/p-7in58j.

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It's still a challenge to detect cholesterol more rapidly and easily. As a result, using a colorimetric sensor to detect cholesterol may result in the development of a ready-to-use. This research shows how a TiO2 nanoparticles may be utilized as a peroxidase mimic to detect H2O2 and free cholesterol. The TiO2 Nanoparticles was carefully studied in terms of structural, morphological, and functional characteristics. In the existence of cholesterol oxidase, and the proposed approach comprises detecting H2O2 produced during cholesterol oxidation. The TiO2 nanoparticles sensor has shown good choles
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Perdani, Meka Saima, Muhammad Faturrohman, Dwini Normayulisa Putri, and Heri Hermansyah. "Oxidation of extracted cholesterol from fatty food by using crude cholesterol oxidase Streptomyces sp." In THE 4TH BIOMEDICAL ENGINEERING’S RECENT PROGRESS IN BIOMATERIALS, DRUGS DEVELOPMENT, HEALTH, AND MEDICAL DEVICES: Proceedings of the International Symposium of Biomedical Engineering (ISBE) 2019. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5139357.

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Raporty organizacyjne na temat "Cholesterol"

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Hausmann, Ricardo, and Eduardo Fernández-Arias. Foreign Direct Investment: Good Cholesterol? Inter-American Development Bank, 2000. http://dx.doi.org/10.18235/0010777.

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This paper studies the proposition that capital inflows tend to take the form of FDI -i.e., the share of FDI in total liabilities tends to be higher- in countries that are safer, more promising and with better institutions and policies. It finds that this view is patently wrong since it stands the historical record on its head. It then uses alternative theories to make sense of the facts. It begins by studying the determinants of the size and composition of the flows of private capital across countries. It finds that while capital flows tend to go to countries that are safer and have better in
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Hung, Hsuan-Yu, Hui-Hsiung Lai, Hui-Chuan Lin, and 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, 2022. http://dx.doi.org/10.37766/inplasy2022.7.0055.

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Review question / Objective: P: ("Hepatitis C"[Mesh] AND "Hepacivirus"[Mesh] AND "Hepatitis C, Chronic”[Mesh]) I: (direct acting antiviral OR asunaprevir OR boceprevir OR daclatasvir OR dasabuvir OR elbasvir OR glecaprevir OR grazoprevir OR ledipasvir OR ombitasvir OR paritaprevir OR pibrentasvir OR simeprevir OR sofosbuvir OR telaprevir OR velpatasvir OR voxilaprevir) C: placebo O: ( "Cholesterol, VLDL"[Mesh] OR "Cholesterol, LDL"[Mesh] OR "Cholesterol, HDL"[Mesh] OR "Dyslipidemias"[Mesh] OR "lipoprotein cholesterol ester, human" [Supplementary Concept] OR "lipoprotein cholesterol" [Supplemen
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Min, Byungrok, Il Suk Kim, and Dong U. Ahn. Dietary Cholesterol Affects Lipid Metabolism in Rabbits. Iowa State University, 2015. http://dx.doi.org/10.31274/ans_air-180814-1348.

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สุขเจริญ, นเรศร, та เอนก อารีพรรค. การกดการสร้างอสุจิด้วย Depot medroxyprogesterone acetate (DMPA) และ Testosterone enanthate. จุฬาลงกรณ์มหาวิทยาลัย, 1998. https://doi.org/10.58837/chula.res.1998.18.

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ได้ทำการศึกษาผลของ Depot medroxyprogesterone acetate (DMPA) กับ Testosterone enanthate (TE) ในการกดการสร้างอสุจิในชายไทย โดยทำการศึกษาในอาสาสมัครชายไทยปกติจำนวน 10 คน ได้แบ่งอาสาสมัครออกเป็น 2 กลุ่ม โดยกลุ่มที่ 1 (จำนวน 5 คน) ได้รับการฉีด DMPA 100 มก. ร่วมกับ TE 125 มก. เข้ากล้ามเนื้อทุก 4 สัปดาห์ และกลุ่มที่ 2 (จำนวน 5 คน) ได้รับการฉีด DMPA 100 มก. ร่วมกับ TE 250 มก. เข้ากล้ามเนื้อทุก 4 สัปดาห์ ทำการตรวจติดตามการเปลี่ยนแปลงของอสุจิเพื่อดูผลของฮอร์โมนต่อการสร้างอสุจิ ค่ามัธยฐานของระยะเวลาตั้งแต่เริ่มฉีดยาจนกระทั่งความเข้มข้นของอสุจิลดลงเป็น 5, 3, 1 และ 0 ล้านตัวต่อ มล. ของทั้งสองกลุ่มเป็น 70,
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ชัยเจริญพงศ์, จรรยา. การสังเคราะห์อนุพันธ์ของคาร์เพสเตอรอลและฤทธิ์ยับยั้งไลเพส : รายงานการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2014. https://doi.org/10.58837/chula.res.2014.94.

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อนุพันธ์ของสารคาร์เพสเตอรอล (13-15) ถูกสังเคราะห์ขึ้นโดยเปลี่ยนหมู่ฟังก์ชันไฮดรอกซิที่ตำแหน่ง C22 ไปเป็นหมู่ acetyl (13) หมู่ benzyl (14) และหมู่ benzoyl (15) สารเหล่านี้แสดงฤทธิ์ยับยั้งไลเพสด้วยค่าเปอร์เซ็นต์การยับยั้งไลเพส เท่ากับ 72.60 ± 5.9%, 87.82 ± 3.00% และ 81.26 ± 3.64% ตามลำดับ ที่ความเข้มข้น 1.25 mg/ml ขณะที่สารคาร์เพสเตอรอลแสดงฤทธิ์ยับยั้งไลเพสด้วยค่าเปอร์เซ็นต์การยับยั้งไลเพส เท่ากับ 62.3 ± 6.2% ที่ความเข้มข้นเดียวกัน นอกจากนี้ยังทดสอบฤทธิ์ยับยั้งไลเพสของสารที่มีโครงสร้างหลักคล้ายคาร์เพสเตอรอล ได้แก่ stigmasterol, β-sitosterol, campesterol และ cholesterol พบว่าสารทั้งสี่มีฤทธิ์ยับย
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Freeman, Michael R. A Cholesterol-Sensitive Regulator of the Androgen Receptor. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada543533.

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Hur, Sun Jin, Kwon Il Seo, and Dong U. Ahn. Effects of Dietary Cholesterol and its Oxidation Products on Pathological Lesions and Cholesterol and Lipid Oxidation in the Rabbit Liver. Iowa State University, 2015. http://dx.doi.org/10.31274/ans_air-180814-1349.

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Lawanprasert, Somsong, Chaiyo Chaichantipyuth, Supatra Srichairat, Nuansri Niwattisaiwong, and Laddawal Phivthong-ngam. Subchronic exposure of Pueraria mirifica in normal - and high cholesterol diet fed rats : influence on hepatic cytochrome P450, lipid profile and toxicity. Chulalongkorn University, 2004. https://doi.org/10.58837/chula.res.2004.28.

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Pueraria mirifica airy shaw and suvatabandhu, know locally as Kwao Keur, is a plant in family Leguminosae. In this study, effects of P.mirifica on hepatic cytochrome P450 (CYP), serum lipid profile and subchronic toxicity were investigated in male Wistar rats. Rats were randomly divided into four treatment groups as following: normal diet-fed group; normal diet-fed supplemented with P.mirifica group; high cholesterol diet-fed group; high cholesterol diet-fed supplemented with P.mirifica group. Each group comprised 10 rats. P.mirifica was administered orally at a dosage of 100 mg/kg/day for 90
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Wood, W. G. Mechanisms of Alcohol Induced Effects on Cellular Cholesterol Dynamics. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada398121.

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Wood, W. G. Mechanisms of Alcohol Induced Effects on Cellular Cholesterol Dynamics. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada431885.

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